WO2019204163A1 - Liquid nitrogen fertilizer compositions and additives therefore - Google Patents
Liquid nitrogen fertilizer compositions and additives therefore Download PDFInfo
- Publication number
- WO2019204163A1 WO2019204163A1 PCT/US2019/027346 US2019027346W WO2019204163A1 WO 2019204163 A1 WO2019204163 A1 WO 2019204163A1 US 2019027346 W US2019027346 W US 2019027346W WO 2019204163 A1 WO2019204163 A1 WO 2019204163A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fertilizer
- urea
- liquid
- inhibitor
- nitrification
- Prior art date
Links
- 239000000654 additive Substances 0.000 title claims abstract description 118
- 239000007788 liquid Substances 0.000 title claims abstract description 114
- 239000000203 mixture Substances 0.000 title claims description 61
- 239000000618 nitrogen fertilizer Substances 0.000 title claims description 20
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 293
- 239000003337 fertilizer Substances 0.000 claims abstract description 264
- 239000004202 carbamide Substances 0.000 claims abstract description 142
- 230000000996 additive effect Effects 0.000 claims abstract description 113
- 239000003112 inhibitor Substances 0.000 claims abstract description 111
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 88
- 239000002601 urease inhibitor Substances 0.000 claims abstract description 77
- 229940090496 Urease inhibitor Drugs 0.000 claims abstract description 46
- 239000006184 cosolvent Substances 0.000 claims abstract description 37
- 239000000243 solution Substances 0.000 claims description 187
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 82
- 150000001875 compounds Chemical class 0.000 claims description 79
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 48
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 47
- 239000011593 sulfur Substances 0.000 claims description 47
- 229910052717 sulfur Inorganic materials 0.000 claims description 47
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 33
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 claims description 28
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 18
- 239000011550 stock solution Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 14
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 14
- 230000008569 process Effects 0.000 claims description 13
- 239000003586 protic polar solvent Substances 0.000 claims description 13
- 239000005077 polysulfide Substances 0.000 claims description 12
- 229920001021 polysulfide Polymers 0.000 claims description 12
- 150000008117 polysulfides Polymers 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 10
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 10
- 239000003086 colorant Substances 0.000 claims description 6
- 239000012736 aqueous medium Substances 0.000 claims description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 4
- DMSZORWOGDLWGN-UHFFFAOYSA-N ctk1a3526 Chemical compound NP(N)(N)=O DMSZORWOGDLWGN-UHFFFAOYSA-N 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 3
- 239000010452 phosphate Substances 0.000 claims description 3
- 238000007865 diluting Methods 0.000 claims description 2
- 239000006193 liquid solution Substances 0.000 claims description 2
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 claims 3
- JLYVRXJEQTZZBE-UHFFFAOYSA-N ctk1c6083 Chemical compound NP(N)(N)=S JLYVRXJEQTZZBE-UHFFFAOYSA-N 0.000 claims 1
- 108010046334 Urease Proteins 0.000 abstract description 19
- 239000000463 material Substances 0.000 abstract description 8
- HEPPIYNOUFWEPP-UHFFFAOYSA-N n-diaminophosphinothioylbutan-1-amine Chemical compound CCCCNP(N)(N)=S HEPPIYNOUFWEPP-UHFFFAOYSA-N 0.000 description 75
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 47
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 42
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 33
- 239000002689 soil Substances 0.000 description 28
- 229910052757 nitrogen Inorganic materials 0.000 description 26
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 23
- 239000002904 solvent Substances 0.000 description 21
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 20
- 229910021529 ammonia Inorganic materials 0.000 description 19
- 239000003960 organic solvent Substances 0.000 description 17
- 239000003795 chemical substances by application Substances 0.000 description 16
- 229910002651 NO3 Inorganic materials 0.000 description 14
- -1 isobutylidene aldehyde Chemical class 0.000 description 14
- 239000000975 dye Substances 0.000 description 13
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 12
- 241000196324 Embryophyta Species 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 10
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 10
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 9
- 229920001276 ammonium polyphosphate Polymers 0.000 description 9
- 239000011575 calcium Substances 0.000 description 8
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 8
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 7
- 229910052791 calcium Inorganic materials 0.000 description 7
- 239000011777 magnesium Substances 0.000 description 7
- 230000000873 masking effect Effects 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 229910052749 magnesium Inorganic materials 0.000 description 6
- 229910052700 potassium Inorganic materials 0.000 description 6
- 239000011591 potassium Substances 0.000 description 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 5
- 239000004114 Ammonium polyphosphate Substances 0.000 description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 230000007062 hydrolysis Effects 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- DCUJJWWUNKIJPH-UHFFFAOYSA-N nitrapyrin Chemical compound ClC1=CC=CC(C(Cl)(Cl)Cl)=N1 DCUJJWWUNKIJPH-UHFFFAOYSA-N 0.000 description 5
- 235000015097 nutrients Nutrition 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 150000001414 amino alcohols Chemical class 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 150000002012 dioxanes Chemical class 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 229940031098 ethanolamine Drugs 0.000 description 4
- 150000002334 glycols Chemical class 0.000 description 4
- PQLMXFQTAMDXIZ-UHFFFAOYSA-N isoamyl butyrate Chemical compound CCCC(=O)OCCC(C)C PQLMXFQTAMDXIZ-UHFFFAOYSA-N 0.000 description 4
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 4
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 4
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 4
- AOSFMYBATFLTAQ-UHFFFAOYSA-N 1-amino-3-(benzimidazol-1-yl)propan-2-ol Chemical compound C1=CC=C2N(CC(O)CN)C=NC2=C1 AOSFMYBATFLTAQ-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 241000282326 Felis catus Species 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- FAYYUXPSKDFLEC-UHFFFAOYSA-L calcium;dioxido-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound [Ca+2].[O-]S([O-])(=O)=S FAYYUXPSKDFLEC-UHFFFAOYSA-L 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- FGRVOLIFQGXPCT-UHFFFAOYSA-L dipotassium;dioxido-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound [K+].[K+].[O-]S([O-])(=O)=S FGRVOLIFQGXPCT-UHFFFAOYSA-L 0.000 description 3
- 231100001261 hazardous Toxicity 0.000 description 3
- 229940062135 magnesium thiosulfate Drugs 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 238000003971 tillage Methods 0.000 description 3
- 229960004418 trolamine Drugs 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 239000004254 Ammonium phosphate Substances 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- QFHMNFAUXJAINK-UHFFFAOYSA-N [1-(carbamoylamino)-2-methylpropyl]urea Chemical compound NC(=O)NC(C(C)C)NC(N)=O QFHMNFAUXJAINK-UHFFFAOYSA-N 0.000 description 2
- MMDJDBSEMBIJBB-UHFFFAOYSA-N [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] Chemical compound [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] MMDJDBSEMBIJBB-UHFFFAOYSA-N 0.000 description 2
- YNNGZCVDIREDDK-UHFFFAOYSA-N aminocarbamodithioic acid Chemical compound NNC(S)=S YNNGZCVDIREDDK-UHFFFAOYSA-N 0.000 description 2
- ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical class [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 2
- 235000019289 ammonium phosphates Nutrition 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 230000003139 buffering effect Effects 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- 238000012272 crop production Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000003673 groundwater Substances 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229940094941 isoamyl butyrate Drugs 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- TZKHCTCLSRVZEY-UHFFFAOYSA-L magnesium;dioxido-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound [Mg+2].[O-]S([O-])(=O)=S TZKHCTCLSRVZEY-UHFFFAOYSA-L 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 150000002823 nitrates Chemical class 0.000 description 2
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 2
- 235000019252 potassium sulphite Nutrition 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 244000000000 soil microbiome Species 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- 239000004034 viscosity adjusting agent Substances 0.000 description 2
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
- VSNHCAURESNICA-NJFSPNSNSA-N 1-oxidanylurea Chemical compound N[14C](=O)NO VSNHCAURESNICA-NJFSPNSNSA-N 0.000 description 1
- AFBBKYQYNPNMAT-UHFFFAOYSA-N 1h-1,2,4-triazol-1-ium-3-thiolate Chemical compound SC=1N=CNN=1 AFBBKYQYNPNMAT-UHFFFAOYSA-N 0.000 description 1
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
- DJEFWCDUJJUZGY-UHFFFAOYSA-N 3-sulfanyl-2h-1,3-benzothiazole Chemical compound C1=CC=C2N(S)CSC2=C1 DJEFWCDUJJUZGY-UHFFFAOYSA-N 0.000 description 1
- MVXMNHYVCLMLDD-UHFFFAOYSA-N 4-methoxynaphthalene-1-carbaldehyde Chemical compound C1=CC=C2C(OC)=CC=C(C=O)C2=C1 MVXMNHYVCLMLDD-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 101000808346 Canavalia ensiformis Urease Proteins 0.000 description 1
- YYLLIJHXUHJATK-UHFFFAOYSA-N Cyclohexyl acetate Chemical compound CC(=O)OC1CCCCC1 YYLLIJHXUHJATK-UHFFFAOYSA-N 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- ZFMSMUAANRJZFM-UHFFFAOYSA-N Estragole Chemical compound COC1=CC=C(CC=C)C=C1 ZFMSMUAANRJZFM-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 235000006679 Mentha X verticillata Nutrition 0.000 description 1
- 235000002899 Mentha suaveolens Nutrition 0.000 description 1
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- 241000605159 Nitrobacter Species 0.000 description 1
- 241000605122 Nitrosomonas Species 0.000 description 1
- 241001495394 Nitrosospira Species 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 244000141698 Prunus lannesiana Species 0.000 description 1
- 235000014001 Prunus serrulata Nutrition 0.000 description 1
- 244000050053 Rosa multiflora Species 0.000 description 1
- 235000000656 Rosa multiflora Nutrition 0.000 description 1
- 235000000659 Rosa rugosa Nutrition 0.000 description 1
- 229910006069 SO3H Inorganic materials 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- JNVCSEDACVAATK-UHFFFAOYSA-L [Ca+2].[S-]SSS[S-] Chemical compound [Ca+2].[S-]SSS[S-] JNVCSEDACVAATK-UHFFFAOYSA-L 0.000 description 1
- PNNCWTXUWKENPE-UHFFFAOYSA-N [N].NC(N)=O Chemical compound [N].NC(N)=O PNNCWTXUWKENPE-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- UZFLPKAIBPNNCA-BQYQJAHWSA-N alpha-ionone Chemical compound CC(=O)\C=C\C1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-BQYQJAHWSA-N 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- AOBXGGAGUYYNQH-UHFFFAOYSA-N ammonium sulfate urea Chemical compound [NH4+].[NH4+].NC(N)=O.[O-]S([O-])(=O)=O AOBXGGAGUYYNQH-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 125000001691 aryl alkyl amino group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- NGLMYMJASOJOJY-UHFFFAOYSA-O azanium;calcium;nitrate Chemical compound [NH4+].[Ca].[O-][N+]([O-])=O NGLMYMJASOJOJY-UHFFFAOYSA-O 0.000 description 1
- CSGLCWIAEFNDIL-UHFFFAOYSA-O azanium;urea;nitrate Chemical compound [NH4+].NC(N)=O.[O-][N+]([O-])=O CSGLCWIAEFNDIL-UHFFFAOYSA-O 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- 229910000085 borane Inorganic materials 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 125000005586 carbonic acid group Chemical group 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 230000000881 depressing effect Effects 0.000 description 1
- 230000001687 destabilization Effects 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229940075933 dithionate Drugs 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000035558 fertility Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910001867 inorganic solvent Inorganic materials 0.000 description 1
- 239000003049 inorganic solvent Substances 0.000 description 1
- 239000003621 irrigation water Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229910001960 metal nitrate Inorganic materials 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000011785 micronutrient Substances 0.000 description 1
- 235000013369 micronutrients Nutrition 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- 239000006012 monoammonium phosphate Substances 0.000 description 1
- 239000002362 mulch Substances 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- MPOFVZMCKSOGHZ-UHFFFAOYSA-N n-diaminophosphinothioylpropan-1-amine Chemical compound CCCNP(N)(N)=S MPOFVZMCKSOGHZ-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000014075 nitrogen utilization Effects 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 230000001863 plant nutrition Effects 0.000 description 1
- 239000010908 plant waste Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical class O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012812 sealant material Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- JNMRHUJNCSQMMB-UHFFFAOYSA-N sulfathiazole Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CS1 JNMRHUJNCSQMMB-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 231100000378 teratogenic Toxicity 0.000 description 1
- 230000003390 teratogenic effect Effects 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- KKEOZWYTZSNYLJ-UHFFFAOYSA-O triazanium;nitrate;sulfate Chemical compound [NH4+].[NH4+].[NH4+].[O-][N+]([O-])=O.[O-]S([O-])(=O)=O KKEOZWYTZSNYLJ-UHFFFAOYSA-O 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- AYTGUZPQPXGYFS-UHFFFAOYSA-N urea nitrate Chemical compound NC(N)=O.O[N+]([O-])=O AYTGUZPQPXGYFS-UHFFFAOYSA-N 0.000 description 1
- WTHDKMILWLGDKL-UHFFFAOYSA-N urea;hydrate Chemical compound O.NC(N)=O WTHDKMILWLGDKL-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05C—NITROGENOUS FERTILISERS
- C05C9/00—Fertilisers containing urea or urea compounds
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05C—NITROGENOUS FERTILISERS
- C05C9/00—Fertilisers containing urea or urea compounds
- C05C9/005—Post-treatment
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05C—NITROGENOUS FERTILISERS
- C05C9/00—Fertilisers containing urea or urea compounds
- C05C9/02—Fertilisers containing urea or urea compounds containing urea-formaldehyde condensates
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
- C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
- C05G3/90—Mixtures of one or more fertilisers with additives not having a specially fertilising activity for affecting the nitrification of ammonium compounds or urea in the soil
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P60/00—Technologies relating to agriculture, livestock or agroalimentary industries
- Y02P60/20—Reduction of greenhouse gas [GHG] emissions in agriculture, e.g. CO2
- Y02P60/21—Dinitrogen oxide [N2O], e.g. using aquaponics, hydroponics or efficiency measures
Definitions
- the present invention is related to liquid nitrogen fertilizer compositions, and a method for producing such fertilizer compositions.
- the present invention furthermore relates to additive packages for liquid nitrogen fertilizer compositions, and to nitrogen fertilizer compositions with urease and/or nitrification inhibitors.
- Urea is a white crystalline solid containing about 46% nitrogen that is widely used in the agricultural industry as a nitrogen fertilizer. World urea consumption is estimated to have exceeded 160 million tons in 2014-2016.
- urea fertilizer can be purchased as prills or as a granulated material.
- Urea can be applied to soil as a solid or as an aqueous solution.
- Aqueous urea solutions also can be applied to certain crops as a foliar spray.
- Urea's high nitrogen content (-46%) helps reduce handling, storage and transportation costs over other dry nitrogen forms. Urea, when properly applied, results in crop yield increases equal to other forms of nitrogen fertilizer.
- Nitrogen from urea can be lost to the atmosphere if urea fertilizer remains on the soil surface for extended periods of time during warm weather. Urea breakdown can begin as soon as it is applied to the soil. Typically, urea does not break down if the soil is totally dry. However, in the presence of the enzyme urease and a small amount of soil moisture, urea normally hydrolyzes to ammonia and carbon dioxide. This can occur in 2 to 4 days; more quickly on high pH soils and at higher temperatures.
- Urease is a nickel-dependent metallo-enzyme, which catalyzes the hydrolysis of urea to ammonia and carbamate. The carbamate then spontaneously hydrolyzes to form carbonic acid and a second molecule of ammonia. At physiological pH, the carbonic acid proton dissociates and the ammonia molecules equilibrate with water, becoming protonated and resulting in a net increase in pH.
- the rate of catalyzed hydrolysis is 10 14 times the rate of the uncatalyzed reaction.
- Nickel-dependent ureases are found in a wide array of different organisms; many have been isolated from various bacteria, fungi, and higher plants.
- nitrate rather than ammonium. Once an ammonium ion is formed, volatilization losses are not a factor and the nitrogen can be utilized for crop growth directly or be converted to nitrate-nitrogen by soil microorganisms. This conversion occurs rapidly in the presence of bacteria and may lead to an excess of nitrate-nitrogen in the soil environment. In order to prevent this rapid conversion, nitrification inhibitors have been developed to inhibit bacterial activity. For example, Nitrosomonas bacteria in the soil transform ammonia into nitrite anion (N0 2 ) that in turn is oxidized to form a nitrate (N0 3 ) anion by Nitrobacter and
- Nitrosolobus bacteria as follows:
- the nitrification rate is most rapid in soils with pH values between 7 and 8, and decreases with decreasing pH values.
- Nitrification of ammonia to nitrate introduces nitrate into the soil, from which the nitrate then leaches into vicinal groundwater.
- urea containing liquid fertilizers like for example UAN, triazone-urea mixtures (like N-sure) and urea-aldehyde adducts.
- Liquid fertilizer solutions and fluid fertilizers are popular in many areas because they are safe to handle, convenient to mix with other nutrients and chemicals and are easily applied.
- a solution of urea [CO(NH 2 ) 2 ] and ammonium nitrate [NH 4 NO 3 ] (UAN) containing between 28 and 32 percent nitrogen (N) is one of the most popular liquid N fertilizers. It is frequently used with other fertilizers, including ammonium thiosulfate.
- UAN ammonium thiosulfate.
- Such solutions of UAN are widely used as a source of N for plant nutrition.
- the NO 3 portion (25 percent of the total N) is immediately available for plant uptake.
- the NH 4 + fraction (25 percent of the total N) can also be assimilated directly by most plants, but is rapidly oxidized by soil bacteria to form NO 3 (nitrate). Soil enzymes hydrolyze the remaining urea portion
- SCU sulfur coated urea
- PCU polymer coated urea
- PSCU sulfur/polymer coated urea
- a device for a slow-release fertilizers based on ammonium for low nitrate plant feeding comprising a hollow body with an opening is described in EP356755.
- the hollow body is filled with the ammonium fertilizer.
- EP476550 describes a soil additive ball for the nitrate-free supply of nitrogen to plants consisting of gypsum to slow down volatilization of urea.
- urease inhibitor prevent or depress the transformation of amide nitrogen in urea to ammonia. They slow down the rate of hydrolysis of urea and reduce the volatilization of ammonia.
- Nitrification inhibitors delay the oxidation of ammonium by depressing the activity of the soil bacteria responsible for nitrification.
- nitrification inhibitors and urease inhibitors.
- agents for improving the nitrogen utilization of mineral and/or organic fertilizers that contain urea are described in EP1183220. These agents comprised alkyl, aryl, and aralkylamino compounds.
- Urea fertilizers containing urease inhibitors comprising metal nitrate are described in GB2285803.
- urease inhibition in urea based fertilizers by phosphorus compounds is described in EP119494, EP119495, EP119487, WO02/083697, WO00/058317, WO97/022568, US569800, US4824783, US5883297, US5883297, US5698003, US4618691, US4540428, US4539037, US4537614, US4530714, US4518413, US4517007, US4517004, US4517003, US45l7,002, US4932992, US4932992 and US4242325.
- Urease and nitrification inhibition of nitrogenous fertilizers with castor oil and oil derived from plants is described in US6315807 and US4932991.
- Use of heterocyclic compounds as urease inhibitors is described in US4932991 and US4954156.
- Organo Boranes or their derivatives are used as an antagonistic inhibitor to urease with urea fertilizers in US4462819.
- a commercially successful urease inhibitor preferably is (1) environmentally and toxicologically safe under a reasonable set of handling conditions, (2) non-phytotoxic, (3) highly active and specific for the urease enzyme, (4) cost effective, (5) nonvolatile and compatible with a wide range of fertilizer materials, and (6) has mobility similar to that of urea.
- N-(n-butyl)-thiophosphoric triamide is a well-known example of urease inhibitors.
- NBPT is commercially available under the trademark Agrotain® available from Agrotain International, St. Louis, MO (Koch).
- Dicyandiamide DCD
- 2-chloro-6-(trichloromethyl)-pyridine nitrapyrin
- DCD diicyandiamide
- nitrapyrin 2-chloro-6-(trichloromethyl)-pyridine
- DMPP 3, 4- dimethylpyrazolphosphate
- NBPT and DCD are organic compounds and not freely soluble in aqueous inorganic fertilizers.
- Several references describe the dissolution of NBPT and/or DCD and its incorporation into urea based liquid fertilizers. Usually organic solvents are used to dissolve these compounds, which either are not compatible with aqueous (water) based fertilizers and/or environmentally hazardous (WO2017/083714, US4517003, W02017/081183, US4530714, US2007/157689, US8048189, US2015/0174140, US2014/40090432).
- Such solutions advantageously can then be added as additive to N- and/or S-containing fertilizers, wherein especially a mixed N-S fertilizer (III) can be advantageous to the end user.
- Additives are easy to use and give less dosage problems. The use of concentrates further reduces transport costs.
- the art does not yet provide a water based solution of such urease and/or nitrification inhibitors, wherein the inhibitors are present in high concentration.
- the art does not yet provide either solutions with reduced amount of organic solvents.
- sulfur containing fertilizers are in use for liquid fertilizer applications, for example (bi)sulfite based liquid fertilizers (like potassium sulfite), polysulfide based liquid fertilizers, and/or thiosulfate based liquid fertilizers.
- Preferred in the present invention are thiosulfate based liquid fertilizers.
- Thiosulfate based liquid fertilizers are well known, and comprise for example:
- Thio-Sul® Ammonium thiosulfate (Thio-Sul®), which is a 50-60% aqueous solution, (grade is 12-0- 0-26S).
- KTS® Potassium thiosulfate
- CaTs® Calcium thiosulfate
- Magnesium thiosulfate which is a 24-25% solution, (grade is 0-0-0- 10S- 4Mg)
- Thiosulfate is an important intermediate in microbial sulfur cycling in soils and sediments. It has been suggested that tetrathionate might be an inhibitor of soil urease by reacting with -SH groups in jackbean urease to form an S-sulpho derivative, as follows:
- Ammonium thiosulfate has been used in conjunction with urea and urea-containing fertilizer products for the purpose of reducing nitrogen loss.
- urea ammonium nitrate fertilizer solution UAN
- addition of ammonium thiosulfate to an urea ammonium nitrate fertilizer solution (UAN) can slow the urea hydrolysis rates after application to soil (Sullivan, D.M., and Havlin, J. L., Soil Sci. Soc. Am. J., 56, 957-960, 1992).
- UAN urea ammonium nitrate fertilizer solution
- the urease inhibition activity of ammonium thiosulfate is not observed in all circumstances, and the effect is considered insufficient.
- thiosulfate may be the effective nitrification inhibitor.
- Liquid sulfur based fertilizers like thiosulfate fertilizers are often combined by a distributor or farmer with other liquid fertilizers, like for example dissolved urea or UAN.
- liquid fertilizer compositions comprising a sulfur based fertilizer, urea and an urease and/or nitrification inhibitor.
- US 5024689 describes liquid fertilizers comprising urea, ammonium thiosulfate, and dicyandi amide.
- Gautney et al. (Ind. Eng. Chem. Prod. Res. Dev. (1985) 24: 155-181) describe the solubility of DCD and some other inhibitors in liquid fertilizers.
- US 5364438 describes a UAN with added NBPT and DCD. The amounts are described as up to 0.4wt% NBPT and up to 2 wt% DCD.
- US 5364438 further describes a UAN with 1.4 wt% of DCD and 2 wt% of ammonium thiosulfate.
- the amount of S in this liquid fertilizer is below 1 wt%.
- the invention relates to an additive solution (I) of at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), said solution comprising: urea (al) and/or an urea-aldehyde adduct (a2) and/or an urea-triazone fertilizer (a3), water (b), at least one organic co-solvent (c), and further
- At least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) wherein compounds (a) are present in an amount of at least about 20 wt%, preferably at least about 25 wt%, relative to the total weight of compounds (a)+(b)+(c), and
- compounds (d) are generally present in an amount of from about 0.04 to about 75 wt%, from about 0.04 to about 60 wt%, usually from about 0.04 to about 40 wt%, preferably from about 0.1 to about 30 wt%, relative to the total weight of the additive solution (I).
- compounds (al) and/or (a3) are preferred over compounds (a2) in view of their capacity to dissolve high amounts of the inhibitors (dl and/or d2).
- Compounds (al), (a2) and (a3) may be referred to herein individually or collectively as“(a)” or“compound (a)” or“compounds (a)”.
- the additive solution hence comprises: urea (al) and/or an urea-triazone fertilizer (a3), water (b), at least one organic co-solvent (c), and further
- the amount of urease inhibitors (dl) is at least about 1 wt%, preferably at least about 2 wt%, at least about 2.5 wt%, at least about 3 wt%, at least about 4 wt%, more preferably at least about 5 wt%, relative to the total weight of the additive solution (I).
- the additive solution comprises: urea (al) and/or an urea-triazone fertilizer (a3), water (b), at least one organic co-solvent (c), and further
- nitrification inhibitor (d2) at least one nitrification inhibitor (d2), or a combination of at least one nitrification (d2) inhibitor and at least one urease inhibitor (dl),
- the amount of nitrification inhibitors (d2) is at least about 0.1 wt%, preferably at least about 1 wt%, more preferably at least about 2 wt%, at least about 2.5 wt%, at least about 3 wt%, at least about 4 wt%, even at least about 5 wt%, relative to the total weight of the additive solution (I).
- the amount of compounds (d) is at most about 80, 75, 70, 65, 60, 55, 50, 49,
- the amount of compounds (d) is at least about 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1 wt% or more.
- the amount of compounds (d) is from about 0.04 to about 50 wt%, preferably from about 0.04 to about 40 wt%, and more preferably from about 0.1 to about 30 wt%.
- the minimal amount of compounds (d) in the additive solution (I) of the invention is at least about 1, 2, 3, 4 or 5wt%.
- the additive solution comprises urease inhibitors (dl) in an amount of at least about 3, 4, 5, 6, 7, 8, 9 wt%, at least about 10 wt%, preferably at least about 15 wt%, up to 30 about wt% and more, and/or a nitrification inhibitors (d2) in an amount of at least about 3, 4,
- the co-solvent generally is a polar protic and/or a polar non-protic solvent that is miscible with water, though some non-polar solvents can be used too.
- the invention furthermore relates to a process for preparing an additive solution (I) as described above, comprising the step of dissolving at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) in a solution comprising: (a) urea (al) and/or an urea- aldehyde adduct (a2) and/or an urea-triazone fertilizer (a3), (b) water and at (c) least one organic co-solvent that preferably is selected from polar protic and/or polar non-protic solvents that are miscible with water.
- Preferred solvents (a) are urea (al), urea-triazone fertilizers or a mixture of both (al+a3).
- the invention furthermore relates to a process for preparing a liquid fertilizer (II) having at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), comprising the step of adding to a liquid fertilizer at least one additive solution (I) as described above.
- the liquid fertilizer (II) comprises a sulfur containing fertilizer, the sulfur containing fertilizer preferably being chosen from polysulfides, (bi)sulfites and/or from thiosulfate fertilizers.
- the sulfur containing fertilizer is selected from thiosulfate fertilizers.
- the sulfur containing fertilizer is selected from (bi)sulfites fertilizers.
- the sulfur containing fertilizer is selected from polysulfide fertilizer.
- the liquid fertilizer (II) comprises a liquid nitrogen containing fertilizer (like UAN) that can be provided in the form of a stock solution that still has to be diluted with water.
- the invention also relates to a liquid fertilizer (II) that is prepared from a process as described herein [any of the above]
- the invention furthermore relates to a liquid mixed N-S fertilizer composition (III) comprising: water,
- a sulfur containing fertilizer selected from polysulfides, (bi)sulfites and/or thiosulfate fertilizers,
- a nitrogen containing fertilizer more in particular an urea based nitrogenous fertilizer
- At least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) wherein the amount of S is more than about 2 wt%, preferably more than about 5 wt%, relative to the total weight of the fertilizer (III), and
- N is more than about 5 wt%, preferably more than about 20 wt%, and more preferably more than about 25 wt%, relative to the total weight of the fertilizer (III).
- the liquid mixed N-S fertilizer composition (III) further comprises at least one co-solvent selected from polar protic and/or from polar non-protic solvents that are miscible with water.
- the liquid mixed N-S fertilizer composition (III) further comprises at least one of compounds (al) and/or (a2) and/or (a3) as defined above.
- the at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) present in said composition (III), are dissolved in an aqueous solution containing at least one of compounds (al) and/or (a2) and/or (a3), and further at least one co-solvent that preferably is selected from polar protic and/or polar non-protic solvents that are miscible with water.
- the composition (III) of the invention is prepared from an additive solution (I) as described above [any of the above]
- the invention furthermore relates to a kit-in-parts containing:
- At least one additive solution (I) as described optionally containing a dye
- liquid sulfur containing fertilizer that preferably is a stock solution of a thiosulfate fertilizer, the liquid sulfur containing fertilizer optionally containing a different dye, and,
- a sheet or a card with dosage recommendations optionally, a sheet or a card with dosage recommendations.
- an urea solution in water in combination with an organic solvent provided a way to permit the dissolution of high concentrations of urease inhibitors like NBPT and/or nitrification inhibitors like DCD. Inhibitor concentrations of up to about 20 wt% and more, even up to about 30 wt% and more could be reached, with substantially lowered amount of organic solvents.
- the urea solution in its most simple form is an aqueous solution of "free" urea in water.
- Urea dissolves well in water.
- the form of urea plays herein no role. Both prills and granules can be used.
- "liquid" urea products available in the market such as the products from Rentech Energy that are provided under the form of a liquid (having ⁇ 52 wt% urea) or under the form of a paste (having ⁇ 69 wt% of urea).
- N-Sure® which is an urea-triazone fertilizer.
- Urea-aldehyde adducts can also be used.
- urea (al) and/or of urea-aldehyde adducts (a2) and/or of urea-triazone fertilizers (a3) is present in the additive solution (I) of the invention, which in a preferred embodiment is an aqueous solution.
- suitable urea-aldehyde adducts are urea-formaldehyde adducts.
- Compounds (al), (a2) and (a3) advantageously are all different from each other.
- the amount of urea (al) and/or urea-aldehyde adducts (a2) and/or of urea-triazone fertilizers (a3) is at least about 25 wt%, more preferably at least about 30 wt%. Weight percentages (wt%) are herein relative to the total weight of compounds (a)+(b)+(c). [0058] Preferred in the context of the invention are urea (al) and/or urea-triazone fertilizers (a3), as these permit dissolving of the highest amounts of NBPT and/or DCD.
- An urea-water solution is one example of a preferred way according to the invention to dissolve the urease (dl) and/or nitrification inhibitors (d2).
- the ratio of water to urea generally will be between about 40 wt% water to about 60 wt% urea and about 60 wt% water to about 40 wt% urea, relative to the total weight of water and urea.
- the preferred ratio of urea to water is about 1 : 1.
- an urea-triazone fertilizer (a3) is used as solvent.
- Urea-triazone is a liquid composition that may contain an amount of water of as low as about 8 wt%.
- an urea (al) solution in water (b) is used for dissolving the above inhibitors (like NBPT and/or DCD).
- an urea-triazone fertilizer generally having from about 5 to about 10 wt% of water is used as solvent by itself or in combination with urea.
- both urea (al) and urea-triazone fertilizers (a3) were used as solvent.
- Compounds (al), (a2) and/or (a3) are preferred over UAN as the latter does not allow to dissolve the same high amounts of the above inhibitors (like NBPT and/or DCD).
- the amount of UAN in the additive solution (I) of the invention is less than about 20 wt%, less than about 15 wt%, less than about 10, 9, 8, 7, 6, 5, 4, 3, 2 or 1 wt%, relative to the total weight of this solution (I). Even more preferably less than about 0.5, 0.4, 0.3, 0.2 or 0.1 wt% of UAN is present in the additive solution (I) of the invention.
- the additive solution will contain about 3 wt% water or more, preferable about 4 wt% or more. If urea is used, the amount of water generally will be about 15 wt% or more, preferably about 20 wt% or more. In one embodiment, the amount of water is about 40 wt% or less, preferably about 35 wt% or less.
- the additive solution further comprises one or more organic solvents (further referred to herein as "co-solvents").
- co-solvents organic solvents
- the combination of dissolved urea and organic solvent is unexpectedly effective to dissolve high amounts of the inhibitors (d) in solution.
- the same is true for the combination of an urea-triazone fertilizer and organic solvents.
- This provides significant benefits, such as the ability to produce a highly stable additive solution.
- This provides significant economic benefits, because the additive solution may be stored in a stable condition for extended periods of time at room temperature, without the need to add stabilizers such as ammonium polyphosphates.
- the co-solvent (c) is herein different from compounds (a) and also different from (b) water (which is an inorganic solvent).
- Co-solvents (c) for use in the additive solution of the invention are preferably chosen from one or more polar protic and/or polar non-protic solvents. Most preferred in the context of the invention are solvents that are miscible with water.
- Protic organic solvents that might be used include C1-C6 alcohols like methanol, ethanol, n-propanol, i-propanol, n-butanol, i-butanol; glycols like ethylene glycol, propylene glycol, glycerol; amino-alcohols like ethanolamine, di- ethanol amine and triethanol amine.
- Other suitable solvents are dimethylsulfonoxide,
- Non-protic polar solvents include dimethylsulfoxide (DMSO), dimethyl formamide (DMF), triethyl phosphate, dioxane and the like.
- Preferred organic co-solvents include ethanol, ethylene glycol, DMSO and/or dioxane. Most preferred are ethanol and/or DMSO for dissolving for increasing the solubility of the inhibitors. Ethanol can work for both NBPT and DCD. DMSO is preferred for DCD.
- the amounts of inhibitors (in particular NBPT and/or DCD) throughout the invention are expressed as weight percentages (wt%) relative to the total weight of the additive solution (I).
- the co-solvent (c) is preferably used in an amount from about 5 to about 60 wt%, preferably in an amount from about 10 to about 55 wt%, and more preferably from about 15 to about 50 wt%, relative to the total weight of the additive solution (I) of the invention. In preferred embodiments, their amount is below about 45 wt%, preferably below about 40 wt%.
- NMP N-methyl-2-pyrrolidone
- PVP polyvinylpyrrolidone
- the amount of NMP and PVP is less than about 10, 9, 9, 7, 6, 5, 4, 3, 2 wt%, more preferably less than about 1 wt%, more preferably less than about 0.5, 0.4, 0.3, 0.2 or 0.1 wt%.
- the additive solution of the invention is substantially free from NMP and PVP, as these can be health deleterious . NMP for instance is listed as teratogenic.
- Solutions (I) of the invention comprise at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (dl). Compounds (dl) and (d2) herein are different from each other, otherwise they would not have been mentioned separately.
- a solution (I) of at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) said solution comprising urea (al), an urea- aldehyde adduct (a2) and/or an urea-triazone fertilizer (a3), water (b) and, ideally, also at least one organic co- solvent (c).
- At least one urease inhibitor (dl) and/or at least one nitrification inhibitor(d2) at least one urease inhibitor (dl) and/or at least one nitrification inhibitor(d2), with compounds (dl) and (d2) advantageously being different from each other.
- compounds (a) are usually present in an amount of at least about 20 wt%, preferably at least about 25 wt%, relative to the total weight of compounds (a)+(b)+(c). For compounds (a3) this amount can even be higher.
- the inhibitors (dl and/or d2) are present in an amount of from about 0.04 to about 70 wt%, from about 0.04 to about 60 wt%, from about 0.04 to about 50 wt%, from about 0.04 to about 40 wt%, relative to the total weight of the solution (I), preferably in an amount of from about 0.1 to about 30 wt%.
- the amount of inhibitors (dl and/or d2) in said solution (I) is at least about 1 wt%, more preferably at least about 2 wt%, at least about 2.5 wt%, at least about 3 wt%, at least about 3.5 wt%, at least about 4 wt%, at least about 4.5 wt%, more preferably at least about 5 wt%. Even more preferably, their amount is at least about 6, 7, 8, 9 or 10 wt%, relative to the total weight of the solution (I). More information on preferred amounts for the different compounds infra.
- additive solutions Such solutions with possibly relative high amounts of nitrification and/or urease inhibitors are named hereinafter "additive solutions”. They can also be referred to as “inhibitor compositions” or “inhibitor solutions”. Preferred in the context of the invention are “water based” solutions.
- the additive solutions (I) of the invention are in the form of "concentrates” that can be added easily to liquid fertilizers (II).
- the liquid fertilizer (II) is provided in the form of a stock solution, meaning that in general water or another aqueous medium is added to become a final liquid fertilizer.
- the inhibitors in question usually are present in an amount of at least about 5, 6, 7, 8, 9 wt%, preferably at least about 10, 11, 12, 13, 14 wt%, or even more preferably at least about 15, 16, 17, 18, 19 wt%, relative to the total weight of the additive solution (I). Even amounts up to about 20 wt%, up to about 25 wt%, up to about 30 wt% and more, or even up to about 40 wt% and more are achievable.
- the urease inhibitors (dl) like NBPT usually are present in an amount from about 0.04 to about 40 wt% in the additive solution, preferably this amount is from about 0.1 to about 30 wt%, and more preferably this amount is from about 0.25 to about 30 wt%. Suitable amounts include for example at least about 1 wt%, preferably at least about 2 wt%, more preferably at least about 3 wt%, and even more preferably at least about 5 wt%.
- concentrates that comprise at least about 10 wt%, at least about 15 wt%, at least about 20 wt%, at least about 25 wt% up to about 30 wt% or more of urease inhibitors such as NBPT.
- the nitrification inhibitors (d2) like DCD preferably are present in amount from about 0.1 to about 40 wt% in the additive solution, more preferably the amount is from about 0.1 to about 30 wt%. Suitable amounts include for example at least about 0.1 wt%, at least about 2 wt%, at least about 3 wt%, or at least about 5 wt%. Preferred though are concentrates that comprise at least about 10 wt%, at least about 15 wt%, at least about 20 wt%, at least about 25 wt% up to at least about 30 wt% or more of nitrification inhibitors such as DCD.
- An embodiment of the invention relates to an additive solution (I) of at least one urease inhibitor (dl), or a combination of at least one urease inhibitor (dl) and at least one nitrification inhibitor (d2), wherein the solution comprises:
- compounds (a) are present in an amount of at least about 20 wt%, relative to the total weight of compounds (a)+(b)+(c), and
- compounds (dl) are present in amount of at least about 0.04 wt%, preferably at least about 1 wt%, more preferably at least about 2 wt%, at least about 3 wt%, relative to the total weight of the solution (I), and
- Another embodiment of the invention relates to an additive solution (I) of at least one nitrification inhibitor (d2), or a combination of at least one nitrification inhibitor (d2) and at least one urease inhibitor (dl), wherein the solution comprises:
- nitrification inhibitor (d2) at least one nitrification inhibitor (d2), and optionally also at least one urease inhibitor
- compounds (a) are present in an amount of at least about 20 wt%, relative to the total weight of compounds (a)+(b)+(c), and
- compounds (d2) are present in amount of at least about 0.1 wt%, preferably at least about 1 wt%, more preferably at least about 2 wt%, at least about 3 wt%, relative to the total weight of the solution (I), and
- Urease inhibitors (dl) are generally chosen from the group of: hydroxyurea, a-hydroxyketone, triketone oximes, hydroquinone (HQ), nitrapyrin and/or phosphoric triamide type inhibitors. Preferred are phosphoric triamide type inhibitors. Preferred urease inhibitors includes phosphoric triamide type inhibitors, preferred are thiophosphoric triamides, more preferred aliphatic thiophosphoric triamides. Particularly preferred are N-alkyl and/or N-acyl thiophosphoric triamides.
- NPPT N-( n-Propyl)-thiophosphoric triamid
- NBPT N-(n-butyl)-thiophosphoric triamide
- NPPT N-(n-Propyl)-thiophosphoric triamid
- NBPT N-(n-butyl)-thiophosphoric triamide
- the urease inhibitor present in the additive solution is NPBT, used alone or in combination with one or more other urease inhibitors.
- compound (dl) advantageously are different from compounds (d2).
- Nitrification inhibitors (d2) are generally chosen from the group of: dicyandiamide (DCD), 3,4-dimethylpyrazzole phosphate (DMPP), 2-chloro-6- (trichloromethyl)-pyridine (N-Serve), thiourea (TU), 2-sulfanilamidothiazole, 4-amino- 1,2,1, triazole, 3 -mercapto- 1,2, 4-triazole, ammonium dithiocarbamate (ADTC), ammonium thiosulfate (ATS) and/or 3-mercapto-benzothiazole (MBT).
- DCD dicyandiamide
- DMPP 3,4-dimethylpyrazzole phosphate
- N-Serve 2-chloro-6- (trichloromethyl)-pyridine
- TU thiourea
- 2-sulfanilamidothiazole 4-amino- 1,2,1, triazole, 3 -mercapto- 1,2, 4-triazole, am
- DCD DCD
- ATS TU and/or DMPP
- DCD DCD
- ATS TU and/or DMPP
- the nitrification inhibitor present in the additive solution is DCD, used alone or in combination with one or more other nitrification inhibitors.
- compound (d2) is DCD, used alone or in combination with one or more other nitrification inhibitors.
- the additive solution (I) comprises NBPT. In another or the same embodiment, the additive solution (I) comprises DCD.
- the additive solution (I) comprises NBPT and no other urease and/or nitrification inhibitors.
- the additive solution comprises DCD and no other nitrification and/or urease inhibitors.
- the additive solution comprises both NBPT and DCD but no other nitrification and/or urease inhibitors.
- the co-solvent (c) that is used in the invention can be any organic solvent that is able to dissolve the inhibitors in question (like NBPT and/or DCD) and that is miscible with water. Suitable candidates can for instance be found amongst polar protic solvents and/or polar non- protic solvents.
- Protic organic solvents include C1-C6 alcohols like methanol, ethanol, n-propanol, i-propanol, n-butanol, i-butanol; glycols like ethylene glycol, propylene glycol, glycerol; amino-alcohols like ethanolamine, di-ethanol amine and tri ethanol amine and the like.
- Non-protic polar solvents include dimethyl sulfoxide (DMSO), dimethyl formamide (DMF), triethyl phosphate, dioxane and the like.
- Particularly suitable are: lower alcohols (especially C1-C6 alcohols, and in particular ethanol), glycols (like e.g., ethylene glycol), dimethylsufonoxide (DMSO), amino-alcohols, dimethylformamide (DMF), dioxanes and/or triethyl phosphate.
- glycols like e.g., ethylene glycol
- DMSO dimethylsufonoxide
- amino-alcohols amino-alcohols
- DMF dimethylformamide
- dioxanes dioxanes and/or triethyl phosphate.
- Preferred are ethanol, glycols like ethylene glycol, DMSO, DMF and/or dioxanes.
- Most preferred are ethanol and/or DMSO.
- C1-C6 alcohols and in particular ethanol were found suitable to dissolve high amounts of urease inhibitors like NBPT. They can be used to dissolve DCD too.
- Organic solvents like DMSO, dioxanes and DMF were found most suitable to dissolve high amounts of nitrification inhibitors like DCD. Particularly preferred for that purpose was DMSO.
- the urease and/or nitrification inhibitors are dissolved in an urea solution in water supplemented with at least one co-solvent to reach high enough concentrations of the inhibitors.
- the urease and/or nitrification inhibitors are dissolved in an urea-triazone fertilizer (having e.g., about 5 to about 10 wt% of water) supplemented with at least one co-solvent to reach high enough concentrations of the inhibitors. In that case no extra addition of water is needed to prepare a solution, as there is enough water in the product.
- a combination of (1) urea in water and of (2) an urea-triazone fertilizer are used to dissolve the inhibitors, and advantageously at least one co-solvent is then used to arrive at high enough concentrations.
- the additive solutions of the invention may further comprise at least one of (e): dyes, colorants, odor masking agents, flow aids, surfactants, silicas, thickeners, viscosity modifiers, pH control agents, etc.
- Preferred compounds (e) are dyes and/or colorants.
- the sum of the weight percentages of compounds (a)+(b)+(c)+(d), when expressed relative to the total weight of the additive solution (I) equals at least about 70 wt%, preferably at least about 80 wt%, more preferably at least about 90 wt%, and most preferably this sum adds up to 100 wt%.
- a process for preparing an additive solution of the invention comprising the step of dissolving at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) in a solution comprising: urea (al) and/or an urea-triazone fertilizer (a3), water(b) and at least one co-solvent (c).
- a solution comprising: urea (al) and/or an urea-triazone fertilizer (a3), water(b) and at least one co-solvent (c).
- urea (al) and/or an urea-triazone fertilizer (a3) water(b) and at least one co-solvent (c).
- urea (al) and/or an urea-triazone fertilizer (a3) water(b) and at least one co-solvent (c).
- urease inhibitors (dl) are there.
- nitrification inhibitor (d2) are present.
- one or more compounds (a3) are used as solvent. Possibly a mix of compounds (al) and (a2) is used in the process of the invention. With the process of the invention any of the earlier described additive solutions (I) of the invention can be prepared.
- a solution of urea (al) in water (b), and at least one organic co-solvent (c) is used to dissolve the inhibitors (d).
- a solution of urea-triazone fertilizer (a3), water (a3, b), and at least one organic co- solvent (c) is used to dissolve the inhibitors (d).
- one or more of the following compounds may be included in the additive solution of the invention: dye, colorant, odor masking agent, flow aid, surfactant, silica, thickener, viscosity modifier, pH control agent, etc (compounds e).
- dye colorant
- odor masking agent flow aid
- surfactant silica
- thickener thickener
- viscosity modifier pH control agent
- pH control agent etc
- An advantage of additive solutions (I) of the invention is also that they are stable at room temperature (RT) for longer periods, without the need for stabilizers like ammonium polyphosphates.
- RT room temperature
- ammonium polyphosphates usually less than about 0.5 wt%, preferably less than about 0.4 wt% of ammonium polyphosphates are present in additive solutions of the invention.
- no ammonium polyphosphates are present in additive solutions of the invention.
- a process for preparing a liquid fertilizer (II) having at least urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) comprising the step of adding an additive solution (I) of the invention (any of the above) to a sulfur containing liquid fertilizer (II).
- an additive solution (I) of the invention any of the above
- DCD containing additive solutions of the invention were found compatible with thiosulfate fertilizers like ammonium thiosulfate.
- a process for preparing a liquid fertilizer (II) having at least one nitrification inhibitor (dl) and/or at least one urease inhibitor (d2) comprising the step of adding an additive solution (I) of the invention (any of the above) to a nitrogen containing liquid fertilizer (II).
- the nitrogen containing liquid fertilizer herein advantageously is different from compounds (d; dl and/or d2).
- a preferred nitrogen fertilizer is one that comprises urea, more in particular urea and ammonium nitrate (like UAN, preferably UAN 28-32). Another example is liquid urea.
- the nitrogen fertilizer can further comprise a sulfur containing fertilizer too.
- the sulfur containing fertilizer in general is chosen from polysulfides, (bi)sulfite and/or thiosulfate fertilizers.
- (bi)sulfite is meant sulfite, bisulfite or a mixture of both.
- the sulfur containing liquid fertilizer herein advantageously is different from compounds (d; dl and/or d2).
- the urease inhibitors (dl) are present in the liquid fertilizer in an amount of from about 0.04 to about 5 wt%, and preferably the nitrification inhibitors (d2) are present in the liquid fertilizer in an amount of from about 0.5 to about 10 wt%, this relative to the total weight of the liquid fertilizer.
- the preferred concentration of NBPT in the liquid fertilizer (II) is from about 0.04 to about 2 wt%, preferably from about 0.04 to about 1.5 wt%.
- the amount of NBPT herein is at least about 0.05 wt%, at least about 0.06 wt%.
- the preferred end concentration for DCD in the liquid fertilizer (II) is from about 0.2 to about 5 wt%, preferably from about 1 to about 2 wt%.
- both urease inhibitors and nitrification inhibitors are present then they are generally present in a ratio of between 1 : 10 to 6: 10, preferably 2: 10 to 3 : 10.
- Provided in the invention are any liquid fertilizers that can be obtained via the process(es) here described.
- the present invention furthermore provides for liquid "concentrated” nitrogen based fertilizers (II), preferably comprising urea, and more preferably comprising urea and ammonium nitrate, to which an additive solution of the present invention (any of the above) is added.
- liquid "concentrated” nitrogen based fertilizers (II) preferably comprising urea, and more preferably comprising urea and ammonium nitrate, to which an additive solution of the present invention (any of the above) is added.
- an additive solution having up to about 30 wt% NBPT and an additive solution having up to about 30 wt% DCD are both prepared, where after at least one of them, possibly both, are added to a stock solution of a liquid fertilizer (II), for example a stock solution comprising an UAN fertilizer, or a stock solution comprising an UAN fertilizer combined with a thiosulfate liquid fertilizer.
- a liquid fertilizer for example a stock solution comprising an UAN fertilizer, or a stock solution comprising an UAN fertilizer combined with a thiosulfate liquid fertilizer.
- an additive solution of urea in water and a co-solvent with up to about 30 wt% NBPT and another one with up to about 30 wt% DCD (possibly with an urea-triazone fertilizer (a3) as solvent instead of an urea solution in water), and combine the required amounts of NBPT and/or DCD solutions with a stock solution of a liquid fertilizer (II), for example one comprising an UAN fertilizer, or an UAN fertilizer combined with a thiosulfate liquid fertilizer (II).
- a liquid fertilizer for example one comprising an UAN fertilizer, or an UAN fertilizer combined with a thiosulfate liquid fertilizer (II).
- an additive solution of urea in water and optionally a co-solvent with up to about 30 wt% NBPT and another one with up to about 30 wt% DCD possibly with urea-triazone fertilizer as solvent instead of an urea solution in water
- a stock solution of a liquid sulfur containing fertilizer for instance a thiosulfate liquid fertilizer to which, optionally, an UAN fertilizer is added.
- This is suitable in particular for use with one or more DCD-based additive solutions of the invention, possibly one containing DCD and NBPT.
- an additive solution of urea in water and optionally a co-solvent with up to about 30 wt% NBPT and another one with up to about 30 wt% DCD possibly with urea-triazone fertilizer as solvent instead of an urea solution in water
- a stock solution of a mixed N-S fertilizer (III) comprising e.g., both an UAN fertilizer and a thiosulfate liquid fertilizer.
- the invention further provides for additive solutions (I) obtainable according to any of the processes described herein and for liquid fertilizers (II) or (III) obtainable according to any of the processes described herein.
- Additive solutions (I) of the invention are in particular suitable for the making of liquid mixed N-S fertilizers (III).
- liquid mixed N-S fertilizer (III) composition comprising: water,
- a sulfur containing fertilizer selected for instance from polysulfide, (bi)sulfite and/or thiosulfate fertilizers,
- NF2 nitrogen containing fertilizer
- At least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) (like NBPT and/or DCD)
- the amount of S is more than about 2 wt%, preferably more than about 5 wt%, relative to the total weight of the fertilizer (III), and
- the amount of N is more than about 5 wt%, preferably more than about 20 wt%, and more preferably more than about 25 wt% relative to the total weight of the fertilizer (III) .
- Such liquid mixed fertilizer (III) can be prepared from one or more additive solutions (I) of the invention (any of those described heretofore).
- Preferred sulfur containing fertilizers are thiosulfates, and more in particular Me- thiosulfates, wherein "Me” is (NH 4 ) 2 , K 2 , Ca, Mg, Mn, Zn, Cu and/or Fe. "Me” preferably is (NH 4 ) 2 , K 2 , Ca, Mg and/or Mn. Preferred are (NH 4 ) 2 , K 2 , Ca and/or Mg. Most preferred is (NH 4 ) 2.
- the thiosulfates are provided in the form of an aqueous solution having > 4 wt% Me-thiosulfate (on solids); preferably more than about 5 wt%, more preferably more than about 10 wt%.
- the thiosulfates are different from compounds (d).
- the sulfur containing fertilizer (SF1) added is different from compounds (d).
- Preferred nitrogen containing fertilizers are urea based fertilizers that can be urea, UAN, N-sure (urea-triazone), urea-methylene etc. Preferred are nitrogenous fertilizers that contain urea and ammonium nitrate, like UAN.
- N-S fertilizer (III) at least one urease inhibitor and/or at least one nitrification inhibitor are present.
- both the sulfur containing fertilizer (SF1) and the nitrogen containing fertilizer (NF2) are liquid fertilizers. They can be added as separate fertilizers, or can be provided under the form of a single liquid N-S fertilizer to which then at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) (like NBPT and/or DCD) are then added.
- part of the fertilizers can be solid in nature.
- a solid urea ammonium sulfate like e.g., a 33-0-0-12S fertilizer
- a solid urea ammonium sulfate like e.g., a 33-0-0-12S fertilizer
- a solid urea ammonium sulfate can be added to or be present in the liquid mixed N-S fertilizer (III) of the invention.
- the urease inhibitor preferably is NBPT and the nitrification preferably is DCD. If NBPT is present, then often in a concentration of more than about 0.04 wt%, more preferably more than about 0.1 wt%, relative to the total weight of the mixed liquid fertilizer (III). If DCD is present, then often in a concentration more than about 0.04 wt%, preferably more than about 0.1 wt%, and more preferably more than about 0.2 wt%, relative to the total weight of the mixed liquid fertilizer (III).
- NBPT is present, either alone or with DCD.
- DCD is present, either alone or with NBPT.
- both NBPT and DCD are present in the mixed N-S liquid fertilizer (III) as described herein.
- the preferred ratio of NBPT to DCD is from 0.1 : 1 to 10: 1; preferred is a ratio of from 0.1 : 1 to 1 : 1, an example of a possible ratio is about 0.25: 1.
- the claimed N-S fertilizers of the invention can be prepared avoiding the use of expensive or hazardous solvents such as DMF, NMP, etc. In fact they can be prepared using environmentally friendly solvents for delivery of the inhibitors (d), such as urea solutions or urea based compounds. Using materials of the invention it is possible to deliver these additives (compounds d) in aqueous N-S fertilizers.
- NBPT for instance is not easy to dissolve in an aqueous solution any may present stability issues with some of the standard liquid fertilizers. Materials of the invention help reduce this incompatibility.
- solutions (I) of the invention proved very stable and led to stable end fertilizers, in particular stable N-S fertilizers.
- stock solutions (I) of the invention brings the necessary flexibility to the end user, they are easy to handle and friendly to man and the environment.
- the mixing, adding of the required amounts of inhibitors from one or more additive solutions (I) of the invention can be done at the level of the liquid fertilizer producer or the distributor.
- another aspect of the invention relates to a container tank holding one or more of the above described fertilizer compositions.
- the container tank can be holding tank.
- the liquid fertilizers (II) or (III) herein described can be pumped to tanker trucks for distribution.
- kits-in-parts containing: at least one additive solution (I) of the invention, optionally containing a dye
- At least one liquid sulfur containing fertilizer (any of those described), optionally containing a different dye, and,
- a sheet or card with dosage recommendations optionally, a sheet or card with dosage recommendations.
- the liquid sulfur containing fertilizer is a liquid thiosulfate fertilizer, most preferably is a stock solution of a liquid thiosulfate fertilizer.
- Liquid fertilizers (II) or (III) as described herein preferably contain from about 28 to about 32 wt% of nitrogen. Preferred is an amount of about 28 wt% of total nitrogen. In another or the same embodiment, liquid fertilizers (II) or (III) as described herein preferably contain from about 1 to about 10 wt% of sulfur, preferably they contain about 5 wt% of total sulfur.
- Yet another aspect of the invention relates to the use of one or more additive solutions (I) of the invention for the making of an 28-0-0-5 S fertilizer.
- the most preferred urease inhibitor is NBPT and the most preferred nitrification inhibitor is DCD.
- the ratio of water : urea : co-solvent is about 1 : 1 : 1. In another preferred embodiment the ratio of water : urea : co-solvent is about 1 : 1 :2.
- the use of ethanol (used in relatively small amounts) further has the advantage that the additive solution obtained is not flammable.
- urease and nitrification inhibitors are combined in one solution, it is preferred to use relative amounts according their required activity, but other relative amounts can be used. Suitable amounts are 10: 1 to 1 :20, preferably 1 : 1 to 1 : 10, like for example about 1 :2 for NBPT to DCD, preferably about 1 :4 for NBPT to DCD. More preferred ratios of the urease inhibitor to nitrification inhibitor given as ratio of NBPT to DCD is between 1 : 10 to 6: 10, more preferably between 2: 10 to 3: 10.
- the additive solution may further comprise further components like for example odor masking agents, colorants, dyes, pH control agents, flow aids, surfactants, and combinations thereof (compounds e).
- the odor of the compositions of the present invention is anyhow relatively low, in comparison to the whole-organic solvent solutions of the prior art. Nevertheless, it can be useful to add such a component, in particular if the additive has further useful properties, like for example also lowering the salt out temperature.
- a preferred odor masking agent includes one of isoamyl butyrate, 4-allylanisole, limonene, terpineol, terpenes, 4-(2, 6, 6-trimethyl -2-cyclo-hex enyl)-3-buten-2-one, benzaldehyde, diethyl malonate, cyclohexyl acetate, anisole, a-ionone, mint oil, Japanese cherry and rose ketones.
- the additive solution comprises an amount of less than about 5 wt% (by total weight of composition) of odor masking agent, preferably, less than about 3 wt%.
- the additive solution comprises an amount of from about 1 wt% to about 3 wt% of the odor masking agent (for example, isoamyl butyrate).
- the odor masking agent preferably lowers the salt-out temperature of the composition
- a dye or colorant is present in the additive solution at an amount of about 0.05 wt% or higher, preferably about 0.1 wt%, or higher (wt% relative to the total composition).
- Preferred are dyes and more in particular food grade dyes.
- the dye - if present - generally is present in the composition in an amount of about 3 wt% or lower, preferably about 1 wt% or lower. Suitable examples include yellow, blue, red and/or green food grade dyes.
- acid control agents acid, base or buffering compounds can be used.
- an acidic compound can be included as a pH control agent to maintain or to adjust the pH of the additive solution.
- Illustrative acids can include, but are not limited to, mineral acids such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, acetic acid, ammonium bisulfite (ABS) or any combination thereof.
- a basic compound can be included as a pH control agent to maintain or to adjust the pH of the additive solution.
- Illustrative base compounds for adjusting the pH can include, but are not limited to, ammonia, amines, e.g., primary, secondary, and tertiary amines and polyamines, sodium hydroxide (NaOH), potassium hydroxide (KOH), or a combination thereof.
- Other Illustrative pH buffering compounds are for instance triethanolamine, sodium borate, potassium bicarbonate, sodium carbonate, potassium carbonate, or any combination thereof.
- the additive solution (I) can be mixed with dissolved fertilizers.
- Fertilizers are common water soluble inorganic fertilizers that provide nitrogen, and optionally further nutrients such as phosphorus, potassium, sulfur and other nutrients.
- Examples of such fertilizers include: for nitrogen as the nutrient: urea, urea-aldehyde oligomers, nitrates and or ammonium salts such as ammonium nitrate, including in combination with urea e.g., as UAN type materials, calcium ammonium nitrate, ammonium sulfate nitrate, ammonium phosphates, like mono-ammonium phosphate, di -ammonium phosphate and ammonium polyphosphate, ammonium sulfate, ammonium thiosulfate, and the like.
- a fertilizer composition can comprise one or a combination of the fertilizers described herein.
- Preferred nitrogenous fertilizers are those containing a nitrogenous compound such as urea, urea-aldehyde oligomers, nitrate salts, ammonium salt, or a mixture thereof, such as ammonium nitrate, ammonium sulfate, ammonium thiosulfate, ammonium polysulfide, ammonium phosphates, ammonium chloride, ammonium bicarbonate, ammonia, calcium nitrate, nitrate soda, calcium cyanamide.
- a nitrogenous compound such as urea, urea-aldehyde oligomers, nitrate salts, ammonium salt, or a mixture thereof, such as ammonium nitrate, ammonium sulfate, ammonium thiosulfate, ammonium polysulfide, ammonium phosphates, ammonium chloride, ammonium bicarbonate, ammonia, calcium nitrate, nitrate soda
- the nitrogenous fertilizer comprises urea (often about 1% to about 23% N solutions), or urea and ammonium nitrate (UAN).
- urea and ammonium nitrate- containing fertilizers include, for example, UAN 18, UAN 28, UAN 30 and UAN 32, triazone, urea methylene, urea-aldehyde adducts and the like.
- Preferred UAN concentrates include UAN 18, UAN 28, UAN 30, UAN 32, and more preferred UAN concentrates are UAN 28 or UAN 32, UAN 32 being most preferred.
- Preferred urea (often about 2% to about 20% N solutions) and urea adducts include N-sure, an urea- triazone fertilizer and Trisert ® triazone fertilizers (often about 5% to about 25% N solutions).
- the urea based fertilizer solution further comprises a sulfur containing fertilizer.
- Suitable sulfur containing fertilizers include polysulfide, (bi)sulfite and/or thiosulfate salts.
- Preferred polysulfide salts include calcium polysulfide (sold for instance under the name Solmenda ® (formerly Soil-MendTM), Sulforix ® or Rex Lime Sulfur) more preferred sulfur containing fertilizer salts include (bi)sulfite and thiosulfates.
- Suitable (bi)sulfite based liquid fertilizer include K-ROW 23 ® (potassium sulfite) and ammonium bisulfite.
- Sulfite components like sodium sulfite have been described as urease inhibitors.
- the inhibitor is believed to bind to the di -nuclear Ni(II) center of some bacterial urease in a tridentate mode involving bonds between the two Ni(II) ions in the active site and all three oxygen atoms of the inhibitor.
- thiosulfate salts include Me thiosulfate, wherein Me is ammonium, potassium, calcium, magnesium, manganese, zinc, copper and/or iron.
- Preferred Me ions include ammonium, potassium, calcium and/or magnesium.
- ammonium thiosulfate is used, because of its additional stabilizing effect on urea.
- Thiosulfate based liquid fertilizers are well known, and comprise for example:
- Thio-Sul® Ammonium thiosulfate (Thio-Sul®), which is a 50-60% aqueous solution, (grade is 12-
- KTS® Potassium thiosulfate
- CaTs® Calcium thiosulfate
- Magnesium thiosulfate which is a 24-25% solution, (grade is 0-0-0- 10S-
- a concentrated fertilizer composition is made by combining the inhibitor composition (additive solution) of the present invention with a concentrated
- a diluted fertilizer composition is prepared by subsequently diluting the concentrated liquid nitrification-inhibited fertilizer composition with an aqueous medium, preferably water in a ratio of up to about 500 pbw, more preferably from about 10 to about 500 pbw and even more preferably from about 100 to about 300 pbw, of the aqueous medium per about 1 pbw concentrated liquid nitrogenous fertilizer composition.
- an aqueous medium preferably water in a ratio of up to about 500 pbw, more preferably from about 10 to about 500 pbw and even more preferably from about 100 to about 300 pbw, of the aqueous medium per about 1 pbw concentrated liquid nitrogenous fertilizer composition.
- the end use fertilizer composition of the present invention is made by combining the additive solution(s) (I) of the present invention, a concentrated liquid nitrogenous fertilizer, and an aqueous medium.
- the end use fertilizer composition of the present invention comprises one or more urease inhibitors, preferably NBPT, alone or in combination with one or more nitrification inhibitors.
- the end use fertilizer composition (II) of the present invention comprises from about 0.001 to about 5 pbw, preferably from about 0.01 to about 2 pbw urease inhibitor and/or nitrification inhibitor per about 100 pbw of the one or more nitrogenous fertilizer compounds.
- the end use fertilizer composition is applied to target plants or to an environment for the target plants, i.e., to ground on or within which the target plants are growing or to be grown, at a rate of from about 0.01 pounds to about 5 pounds of the fertilizer composition, preferably from about 0.05 pounds to about 2 pounds of the fertilizer composition, per 1000 square feet of ground.
- the end use fertilizer composition is applied to target plants or to an environment for the target plants at a rate effective to provide a dosage of fertilizer of from about 0.01 pounds to about 5 pounds of fertilizer, preferably from about 0.05 pounds to about 2 pounds of fertilizer, per 1000 square feet of ground.
- composition of the present invention provides improved ease of handling of urease inhibitors and/or nitrification inhibitors, improved solubility characteristics, low toxicity of the water based solution with only a relatively low amount of organic solvents, good storage characteristics, and excellent miscibility with aqueous compositions, such as aqueous nitrogenous fertilizer formulations.
- compositions are described as percent by weight on a ton basis.
- Additive solutions (I) of the invention and liquid fertilizers (II) of the invention help stimulate plant growth, and reduce ammonia loss and slow down nitrification.
- formulations of the current invention are for illustration only and not limited to just these formulations but includes all known formulations that are suitable for obtaining good inhibition of urease and of nitrification.
- the products listed below are not limited to just these products but includes all liquid fertilizers and suspension fertilizers commonly used in the liquid fertilizer industry that would require the use of NBPT as an urease inhibitor to reduce or minimize ammonia loss or the use of DCD as a nitrification inhibitor to slow or reduce nitrification reaction in the soil.
- compositions can be made by mixing concentrated additive solutions with urea and/or UAN solutions.
- nitrogen content can range from about 1% N as UAN1 to about 31.9% N as UAN32, preferably between about 5 and about 31.9% and more preferably between about 16 and about 31.9%.
- nitrogen content can range about 1% to about 23%, preferably between about 5% and about 23% and more preferably between about 15 and about 20%.
- Ranges for liquid phosphate are from about 0.1% to about 33.9% while ranges for potassium are from about 0.1% to about 24.9% using potassium thiosulfate and from about 0.1% to about 22.9% using potassium bi/sulfite.
- Ranges for NBPT are from about 0.01% to about 5%, for DCD from about 0.1 to about 20% and for Thio-Sul from about 1.0% to about 25.9% sulfur.
- Other nutrients and micronutrients that can be added include zinc, boron, calcium, iron, copper, molybdenum, manganese, and magnesium.
- compositions are relatively high strength compositions, and particularly preferred are high strength compositions with a relatively high amount of sulfur.
- Urea is dissolved in the same amount of water by stirring. Thereafter - if applicable - the co- solvent is mixed, and thereafter the urease and/or nitrification inhibitor.
- the amounts are given in the Table below.
- N-Sure® an urea-triazone fertilizer contains about 8% water; hence, of the 20 wt% about 1.6 wt% is water.
- the resulting solutions are clear to the eye.
- the solutions are storage stable at temperatures between about 15 °C and about 40 °C.
- the solution can be used to add a required amount of NBPT and/or DCD to a liquid fertilizer as wanted.
- Example 9 As an alternative to Example 9, a stock solution of 10 kg urea and 10 L of water 10 kg of ethanol with 5 kg DCD and 1.25 kg NBPT was prepared by stirring first water and urea, adding ethanol and thereafter adding DCD and NBPT and further stirring, till a clear solution was obtained.
- a solution of 187.6 kg urea, 52.4 kg ammonium thiosulfate and 189.46 kg water was prepared. To this mixture, the 25 kg of stock solution was added. The resulting solution was clear and storage stable.
- the additive solutions (I) of the invention could be stored for several months, even up to 1 year without phase separation and/or precipitation.
- An additive solution according to the invention containing about 20 wt% of NBPT in urea/ethanol, was subjected to a HPLC method to see if the NBPT had remained stable.
- Gradient HPLC was used for these purposes. Were used herein: a propylamine column, a Diode Array Detector set at 2014 nm, and acetonitrile : water as mobile phase.
- the gradient table is the one below: [00180] Gradient Table:
- Additive solutions (I) of the invention are thus both chemically and physically stable when stored in closed containers under normal conditions of pressure and temperature (about 1 bar, about l8-25°C). This is surprising, as water was thought to facilitate the decomposition of NBPT into a non-effective substance. Without being bound by theory, it is believed that compounds (a) protect compounds (d) from destabilization, even sensitive compounds like NBPT.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Soil Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Fertilizers (AREA)
Abstract
The present invention relates to additive solutions of at least one urease inhibitor and/or at least one nitrification inhibitor, wherein the solution comprises: urea, an urea-aldehyde adduct and/or an urea-triazone fertilizer, water and at least one co-solvent, and further at least about 2.5 wt%, preferably at least about 5 wt% of urease and/or nitrification inhibitors. Up to about 30 wt% and more of the inhibitors could be dissolved as such. Additive solutions of the invention are highly suitable for the adding to liquid N and/or S fertilizers. A liquid 28-0-0-5S fertilizer can for instance be made from materials of the invention.
Description
TITLE OF THE INVENTION
LIQUID NITROGEN FERTILIZER COMPOSITIONS AND ADDITIVES THEREFORE
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application claims priority to U.S. provisional application no. 62/660,663 filed April 20, 2018, which is hereby incorporated herein by reference for all that it discloses.
FIELD OF THE INVENTION
[0002] The present invention is related to liquid nitrogen fertilizer compositions, and a method for producing such fertilizer compositions. The present invention furthermore relates to additive packages for liquid nitrogen fertilizer compositions, and to nitrogen fertilizer compositions with urease and/or nitrification inhibitors.
BACKGROUND OF THE INVENTION
[0003] Urea is a white crystalline solid containing about 46% nitrogen that is widely used in the agricultural industry as a nitrogen fertilizer. World urea consumption is estimated to have exceeded 160 million tons in 2014-2016. Commercially, urea fertilizer can be purchased as prills or as a granulated material. Urea can be applied to soil as a solid or as an aqueous solution. Aqueous urea solutions also can be applied to certain crops as a foliar spray. Urea's high nitrogen content (-46%) helps reduce handling, storage and transportation costs over other dry nitrogen forms. Urea, when properly applied, results in crop yield increases equal to other forms of nitrogen fertilizer.
[0004] The stability of urea today is receiving greater attention due to a major increase in no- tillage or minimum-tillage crop production. In no- or minimum-tillage crop production, fertilizer materials are placed on the soil surface, as opposed to placement in the soil for conventional seedbed operations. Also, improved stability of urea has major nitrogen efficiency implications for the turf industry, where fertilizer products are placed on the soil and turf surface.
[0005] Nitrogen from urea can be lost to the atmosphere if urea fertilizer remains on the soil surface for extended periods of time during warm weather. Urea breakdown can begin as soon as it is applied to the soil. Typically, urea does not break down if the soil is totally dry. However, in
the presence of the enzyme urease and a small amount of soil moisture, urea normally hydrolyzes to ammonia and carbon dioxide. This can occur in 2 to 4 days; more quickly on high pH soils and at higher temperatures.
[0006] Urease is a nickel-dependent metallo-enzyme, which catalyzes the hydrolysis of urea to ammonia and carbamate. The carbamate then spontaneously hydrolyzes to form carbonic acid and a second molecule of ammonia. At physiological pH, the carbonic acid proton dissociates and the ammonia molecules equilibrate with water, becoming protonated and resulting in a net increase in pH.
[0007] The rate of catalyzed hydrolysis is 1014 times the rate of the uncatalyzed reaction.
Nickel-dependent ureases are found in a wide array of different organisms; many have been isolated from various bacteria, fungi, and higher plants.
[0008] When urea hydrolysis takes place on the soil surface, NH3 can escape into the atmosphere. Such escape into the atmosphere is called ammonia volatilization. This type of nitrogen fertilizer loss does not occur if urea or urea-containing materials are placed below the soil surface, as in typical seed bed operations. Direct placement of urea below the soil surface is the most secure way to prevent nitrogen loss by way of ammonia volatilization. Nitrogen losses also are minimized if rainfall occurs soon after a surface application or if overhead irrigation water is applied.
[0009] When placed in the soil environment, ammonia further undergoes the following reaction:
NH3 + ¾0 NH4 + + OH
[0010] Many crops prefer nitrate rather than ammonium. Once an ammonium ion is formed, volatilization losses are not a factor and the nitrogen can be utilized for crop growth directly or
be converted to nitrate-nitrogen by soil microorganisms. This conversion occurs rapidly in the presence of bacteria and may lead to an excess of nitrate-nitrogen in the soil environment. In order to prevent this rapid conversion, nitrification inhibitors have been developed to inhibit bacterial activity. For example, Nitrosomonas bacteria in the soil transform ammonia into nitrite anion (N02 ) that in turn is oxidized to form a nitrate (N03 ) anion by Nitrobacter and
Nitrosolobus bacteria, as follows:
2NH4 + 302 2N03 + 8H+
[0011] The nitrification rate is most rapid in soils with pH values between 7 and 8, and decreases with decreasing pH values.
[0012] Leaching of nitrate into groundwater has drawn the attention of public health officials. Therefore, reduction of the nitrification rate is desirable. Nitrification of ammonia to nitrate introduces nitrate into the soil, from which the nitrate then leaches into vicinal groundwater.
[0013] Several urea containing liquid fertilizers exist, like for example UAN, triazone-urea mixtures (like N-sure) and urea-aldehyde adducts. Liquid fertilizer solutions and fluid fertilizers are popular in many areas because they are safe to handle, convenient to mix with other nutrients and chemicals and are easily applied. A solution of urea [CO(NH2)2] and ammonium nitrate [NH4NO3] (UAN) containing between 28 and 32 percent nitrogen (N) is one of the most popular liquid N fertilizers. It is frequently used with other fertilizers, including ammonium thiosulfate. Such solutions of UAN are widely used as a source of N for plant nutrition. The NO3 portion (25 percent of the total N) is immediately available for plant uptake. The NH4 + fraction (25 percent of the total N) can also be assimilated directly by most plants, but is rapidly oxidized by soil bacteria to form NO3 (nitrate). Soil enzymes hydrolyze the remaining urea portion
(approximately 50 percent of the total N but can vary between as little as 10% to as much as 90% urea- nitrogen depending on the manufacturer) to form NH4 +, which subsequently transforms to NO3 in most soil conditions.
[0014] Many different ways have been proposed to combat extensive nitrogen loss to the atmosphere and/or nitrification.
[0015] For instance, several types of slow release fertilizers have been introduced onto the market. Chemical reaction of urea with aldehydes, including formaldehyde as liquid (formalin),
and as partially condensed with urea (UFC, UF 85), making UF fertilizers, and with acetaldehyde making urea-crotonaldehyde (CDU), or with isobutylidene aldehyde making isobutylidene diurea fertilizers (IBDU) have been employed for the chemical protection of urea providing slow release nitrogen (SRN) fertilizers. The foregoing are examples of fertilizers produced by the reaction of urea with aldehydes. Products from the reaction of urea with aldehydes are also known as urea-aldehyde adducts.
[0016] Physical barriers such as sulfur coating, polymer coating, and sulfur polymer coating have been applied to urea forming sulfur coated urea (SCU), polymer coated urea (PCU), and sulfur/polymer coated urea (PSCU) in order to slow down the hydrolyses of surface applied urea fertilizers.
[0017] A device for a slow-release fertilizers based on ammonium for low nitrate plant feeding comprising a hollow body with an opening is described in EP356755. The hollow body is filled with the ammonium fertilizer. EP476550 describes a soil additive ball for the nitrate-free supply of nitrogen to plants consisting of gypsum to slow down volatilization of urea.
[0018] Polymer coatings for controlled fertilizer release are described in EP357687,
W089/003811, W097/004819, US6262183 and US5435821. Sulfur coated urea fertilizers are described in W002/090294. ETse of coating, binding and sealant materials such as Palm Oil for urea fertilizers are described in GB2164640.
[0019] Furthermore, a number of additives have been described, that are aimed at reducing the conversion from urea to ammonia (urease inhibitor) and/or to reduce the oxidation from ammonia to nitrate (nitrification inhibitor). Thus, urease inhibitors prevent or depress the transformation of amide nitrogen in urea to ammonia. They slow down the rate of hydrolysis of urea and reduce the volatilization of ammonia. Nitrification inhibitors delay the oxidation of ammonium by depressing the activity of the soil bacteria responsible for nitrification.
[0020] Numerous products have been promoted as nitrification inhibitors and urease inhibitors. For example, agents for improving the nitrogen utilization of mineral and/or organic fertilizers that contain urea are described in EP1183220. These agents comprised alkyl, aryl, and
aralkylamino compounds. Urea fertilizers containing urease inhibitors comprising metal nitrate are described in GB2285803.
[0021] Similarly, many compounds, including organic compounds, inorganic materials, metal ions, organophosphorus compounds, and agriculture chemicals, have been tested as soil urease inhibitors (Bock, B. R. and D. E. Kissel, Ammonia Volatilization from Urea Fertilizers. Bulletin Y-206, National Fertilizer Development Center, TVA, Muscle Shoals, AL. 1988). For example, urease inhibition in urea based fertilizers by phosphorus compounds is described in EP119494, EP119495, EP119487, WO02/083697, WO00/058317, WO97/022568, US569800, US4824783, US5883297, US5883297, US5698003, US4618691, US4540428, US4539037, US4537614, US4530714, US4518413, US4517007, US4517004, US4517003, US45l7,002, US4932992, US4932992 and US4242325.
[0022] Urease and nitrification inhibition of nitrogenous fertilizers with castor oil and oil derived from plants is described in US6315807 and US4932991. Use of heterocyclic compounds as urease inhibitors is described in US4932991 and US4954156. Organo Boranes or their derivatives are used as an antagonistic inhibitor to urease with urea fertilizers in US4462819.
[0023] A commercially successful urease inhibitor preferably is (1) environmentally and toxicologically safe under a reasonable set of handling conditions, (2) non-phytotoxic, (3) highly active and specific for the urease enzyme, (4) cost effective, (5) nonvolatile and compatible with a wide range of fertilizer materials, and (6) has mobility similar to that of urea.
[0024] N-(n-butyl)-thiophosphoric triamide (NBPT) is a well-known example of urease inhibitors. NBPT is commercially available under the trademark Agrotain® available from Agrotain International, St. Louis, MO (Koch).
[0025] Dicyandiamide (DCD) and 2-chloro-6-(trichloromethyl)-pyridine (nitrapyrin) are two examples of well-known nitrification inhibitors. Also well-known is 3, 4- dimethylpyrazolphosphate (DMPP).
[0026] It is prudent to stabilize the urea content of UAN by nitrogen stabilizers such as NBPT, DCD or both.
[0027] Yet, NBPT and DCD are organic compounds and not freely soluble in aqueous inorganic fertilizers. Several references describe the dissolution of NBPT and/or DCD and its incorporation into urea based liquid fertilizers. Mostly organic solvents are used to dissolve these compounds, which either are not compatible with aqueous (water) based fertilizers and/or environmentally hazardous (WO2017/083714, US4517003, W02017/081183, US4530714, US2007/157689, US8048189, US2015/0174140, US2014/40090432).
[0028] Other references disclose the dissolution of NBPT and DCD in protic or non-protic organic water miscible solvents, like alcohols, amino alcohols, DMSO, triethyl phosfate and N- methyl-2-pyrrolidone (NMP). Examples are US2010/206031, US2014/0090432,
US2014/0037570, WO 2014/028767, W02014/100561, W02016/054012, W0017/031186, and US2018/002246. These solutions of one or more organic solvents generally still have a flash point, and are flammable. Some of these solutions make use of relatively expensive solvents.
[0029] There is a demand for the dissolution of NBPT and/or DCD in materials that are less hazardous, cheaper and that lead to non-flammable products. There is further a demand for solutions that are compatible with aqueous (water) based fertilizers.
[0030] Such solutions advantageously can then be added as additive to N- and/or S-containing fertilizers, wherein especially a mixed N-S fertilizer (III) can be advantageous to the end user. Additives are easy to use and give less dosage problems. The use of concentrates further reduces transport costs.
[0031] The art does not yet provide a water based solution of such urease and/or nitrification inhibitors, wherein the inhibitors are present in high concentration. The art does not yet provide either solutions with reduced amount of organic solvents. Today no solution has been provided for combining such inhibitors to sulfur based liquid fertilizers, as this has been seen as problematic and difficult.
[0032] Several sulfur containing fertilizers are in use for liquid fertilizer applications, for example (bi)sulfite based liquid fertilizers (like potassium sulfite), polysulfide based liquid fertilizers, and/or thiosulfate based liquid fertilizers. Preferred in the present invention are thiosulfate based liquid fertilizers.
[0033] Thiosulfate based liquid fertilizers are well known, and comprise for example:
Ammonium thiosulfate (Thio-Sul®), which is a 50-60% aqueous solution, (grade is 12-0- 0-26S).
- Potassium thiosulfate (KTS®), which is a 50% aqueous solution, (grade is 0-0-25-17S).
Calcium thiosulfate (CaTs®), which is a 24-25% aqueous solution, (grade is 0-0-0-10S- 6Ca)
- Magnesium thiosulfate (MagThio®), which is a 24-25% solution, (grade is 0-0-0- 10S- 4Mg)
[0034] Thiosulfates readily oxidize to dithionate, then to tetrathionate, and finally to sulfates, in accordance with the following sequence:
S203 2 + O2 S406 2 S04 '2
[0035] This transformation makes thiosulfates useful as fertilizers especially in combination with cations such as ammonium, potassium, calcium, and magnesium.
[0036] Thiosulfate is an important intermediate in microbial sulfur cycling in soils and sediments. It has been suggested that tetrathionate might be an inhibitor of soil urease by reacting with -SH groups in jackbean urease to form an S-sulpho derivative, as follows:
RSH + S406-2 RS-S2O3H + S203 '2
RS-S2O3H + O2 RS-SO3H + S02
[0037] Ammonium thiosulfate has been used in conjunction with urea and urea-containing fertilizer products for the purpose of reducing nitrogen loss. For example, it has been suggested that addition of ammonium thiosulfate to an urea ammonium nitrate fertilizer solution (UAN) can slow the urea hydrolysis rates after application to soil (Sullivan, D.M., and Havlin, J. L., Soil Sci. Soc. Am. J., 56, 957-960, 1992). However, the urease inhibition activity of ammonium thiosulfate is not observed in all circumstances, and the effect is considered insufficient. For example, ammonium thiosulfate was ineffective when applied on a vegetable mulch, wheat stubble, or crop residue (Goos, R.J., 1987. Proceedings of the l7thN. Central Extension Industry
Soil Fertility Workshop, October 28-29, 1987). Although some suggestions have been made, the precise cause for the varying results is unclear. Yet, thiosulfate, may be the effective nitrification inhibitor.
[0038] Liquid sulfur based fertilizers like thiosulfate fertilizers are often combined by a distributor or farmer with other liquid fertilizers, like for example dissolved urea or UAN.
[0039] Only a few references describe liquid fertilizer compositions comprising a sulfur based fertilizer, urea and an urease and/or nitrification inhibitor. US 5024689 describes liquid fertilizers comprising urea, ammonium thiosulfate, and dicyandi amide. Gautney et al. (Ind. Eng. Chem. Prod. Res. Dev. (1985) 24: 155-181) describe the solubility of DCD and some other inhibitors in liquid fertilizers. US 5364438 describes a UAN with added NBPT and DCD. The amounts are described as up to 0.4wt% NBPT and up to 2 wt% DCD. US 5364438 further describes a UAN with 1.4 wt% of DCD and 2 wt% of ammonium thiosulfate. The amount of S in this liquid fertilizer is below 1 wt%. These are end fertilizers and not additive solutions for delivering NBPT and/or DCD.
[0040] There is a need for water based solutions of urease inhibitors like NBPT and/or nitrification inhibitors like DCD that can be mixed with other water based liquid fertilizer compositions in varying amounts, including the above sulfur containing liquid fertilizers.
[0041] There is furthermore a need for concentrated solutions comprising urea and sulfur containing fertilizers, with in particular relatively large amounts of sulfur, having an improved long availability of nitrogen fertilizer.
SUMMARY OF THE INVENTION
[0042] In a first aspect, the invention relates to an additive solution (I) of at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), said solution comprising: urea (al) and/or an urea-aldehyde adduct (a2) and/or an urea-triazone fertilizer (a3), water (b), at least one organic co-solvent (c), and further
at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2),
wherein compounds (a) are present in an amount of at least about 20 wt%, preferably at least about 25 wt%, relative to the total weight of compounds (a)+(b)+(c), and
wherein compounds (d) are generally present in an amount of from about 0.04 to about 75 wt%, from about 0.04 to about 60 wt%, usually from about 0.04 to about 40 wt%, preferably from about 0.1 to about 30 wt%, relative to the total weight of the additive solution (I).
[0043] Within the context of the invention, compounds (al) and/or (a3) are preferred over compounds (a2) in view of their capacity to dissolve high amounts of the inhibitors (dl and/or d2). Compounds (al), (a2) and (a3) may be referred to herein individually or collectively as“(a)” or“compound (a)” or“compounds (a)”.
[0044] Preferably, the additive solution hence comprises: urea (al) and/or an urea-triazone fertilizer (a3), water (b), at least one organic co-solvent (c), and further
at least one urease inhibitor (dl), or a combination of at least one urease inhibitor (dl) and at least one nitrification inhibitor (d2),
wherein the amount of urease inhibitors (dl) is at least about 1 wt%, preferably at least about 2 wt%, at least about 2.5 wt%, at least about 3 wt%, at least about 4 wt%, more preferably at least about 5 wt%, relative to the total weight of the additive solution (I).
[0045] In a further embodiment, preferably, the additive solution comprises: urea (al) and/or an urea-triazone fertilizer (a3), water (b), at least one organic co-solvent (c), and further
at least one nitrification inhibitor (d2), or a combination of at least one nitrification (d2) inhibitor and at least one urease inhibitor (dl),
wherein the amount of nitrification inhibitors (d2) is at least about 0.1 wt%, preferably at least about 1 wt%, more preferably at least about 2 wt%, at least about 2.5 wt%, at least about 3 wt%, at least about 4 wt%, even at least about 5 wt%, relative to the total weight of the additive solution (I).
[0046] Usually, the amount of compounds (d) is at most about 80, 75, 70, 65, 60, 55, 50, 49,
48, 47, 46 or 45 wt%, relative to the total weight of the additive solution (I). Preferably, the
amount of compounds (d) is at least about 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1 wt% or more. Preferably, the amount of compounds (d) is from about 0.04 to about 50 wt%, preferably from about 0.04 to about 40 wt%, and more preferably from about 0.1 to about 30 wt%. Usually the minimal amount of compounds (d) in the additive solution (I) of the invention is at least about 1, 2, 3, 4 or 5wt%.
[0047] Preferably, the additive solution comprises urease inhibitors (dl) in an amount of at least about 3, 4, 5, 6, 7, 8, 9 wt%, at least about 10 wt%, preferably at least about 15 wt%, up to 30 about wt% and more, and/or a nitrification inhibitors (d2) in an amount of at least about 3, 4,
5, 6, 7, 8, 9 wt%, at least about 10 wt%, preferably at least about 15 wt%, up to about 30 wt% and more, relative to the total weight of the additive solution (I).
[0048] The co-solvent generally is a polar protic and/or a polar non-protic solvent that is miscible with water, though some non-polar solvents can be used too.
[0049] The invention furthermore relates to a process for preparing an additive solution (I) as described above, comprising the step of dissolving at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) in a solution comprising: (a) urea (al) and/or an urea- aldehyde adduct (a2) and/or an urea-triazone fertilizer (a3), (b) water and at (c) least one organic co-solvent that preferably is selected from polar protic and/or polar non-protic solvents that are miscible with water. Preferred solvents (a) are urea (al), urea-triazone fertilizers or a mixture of both (al+a3).
[0050] Preferred is hence a process for preparing an additive solution as described above (I), comprising the step of dissolving at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) in a solution comprising: (a) urea (al), and/or an urea-triazone fertilizer (a3), (b) water and at (c) least one organic co-solvent that preferably is selected from polar protic and/or polar non-protic solvents that are miscible with water.
[0051] The invention furthermore relates to a process for preparing a liquid fertilizer (II) having at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), comprising the step of adding to a liquid fertilizer at least one additive solution (I) as described above. In an embodiment of the invention, the liquid fertilizer (II) comprises a sulfur containing
fertilizer, the sulfur containing fertilizer preferably being chosen from polysulfides, (bi)sulfites and/or from thiosulfate fertilizers. In one embodiment of the invention the sulfur containing fertilizer is selected from thiosulfate fertilizers. In another embodiment, the sulfur containing fertilizer is selected from (bi)sulfites fertilizers. In yet another embodiment, the sulfur containing fertilizer is selected from polysulfide fertilizer. In the same or another embodiment of the invention, the liquid fertilizer (II) comprises a liquid nitrogen containing fertilizer (like UAN) that can be provided in the form of a stock solution that still has to be diluted with water. The invention also relates to a liquid fertilizer (II) that is prepared from a process as described herein [any of the above]
[0052] The invention furthermore relates to a liquid mixed N-S fertilizer composition (III) comprising: water,
a sulfur containing fertilizer, selected from polysulfides, (bi)sulfites and/or thiosulfate fertilizers,
a nitrogen containing fertilizer, more in particular an urea based nitrogenous fertilizer, and
at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), wherein the amount of S is more than about 2 wt%, preferably more than about 5 wt%, relative to the total weight of the fertilizer (III), and
wherein the amount of N is more than about 5 wt%, preferably more than about 20 wt%, and more preferably more than about 25 wt%, relative to the total weight of the fertilizer (III).
[0053] Preferably the liquid mixed N-S fertilizer composition (III) further comprises at least one co-solvent selected from polar protic and/or from polar non-protic solvents that are miscible with water. Preferably the liquid mixed N-S fertilizer composition (III) further comprises at least one of compounds (al) and/or (a2) and/or (a3) as defined above. In a preferred embodiment, the at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) present in said composition (III), are dissolved in an aqueous solution containing at least one of compounds (al) and/or (a2) and/or (a3), and further at least one co-solvent that preferably is selected from polar protic and/or polar non-protic solvents that are miscible with water. In a preferred embodiment
of the invention, the composition (III) of the invention is prepared from an additive solution (I) as described above [any of the above]
[0054] The invention furthermore relates to a kit-in-parts containing:
at least one additive solution (I) as described, optionally containing a dye,
at least one liquid sulfur containing fertilizer, that preferably is a stock solution of a thiosulfate fertilizer, the liquid sulfur containing fertilizer optionally containing a different dye, and,
optionally, a sheet or a card with dosage recommendations.
DETAILED DESCRIPTION OF THE INVENTION
[0055] The inventors discovered that an urea solution in water, in combination with an organic solvent provided a way to permit the dissolution of high concentrations of urease inhibitors like NBPT and/or nitrification inhibitors like DCD. Inhibitor concentrations of up to about 20 wt% and more, even up to about 30 wt% and more could be reached, with substantially lowered amount of organic solvents.
[0056] The urea solution in its most simple form is an aqueous solution of "free" urea in water. Urea dissolves well in water. The form of urea plays herein no role. Both prills and granules can be used. Alternatively one can use "liquid" urea products available in the market such as the products from Rentech Energy that are provided under the form of a liquid (having ~52 wt% urea) or under the form of a paste (having ~69 wt% of urea). Also suitable was N-Sure®, which is an urea-triazone fertilizer. Urea-aldehyde adducts can also be used.
[0057] Preferably at least about 20 wt% of urea (al) and/or of urea-aldehyde adducts (a2) and/or of urea-triazone fertilizers (a3) is present in the additive solution (I) of the invention, which in a preferred embodiment is an aqueous solution. Examples of suitable urea-aldehyde adducts are urea-formaldehyde adducts. Compounds (al), (a2) and (a3) advantageously are all different from each other. The term‘urea’ in particular refers to‘free urea’, not to urea adducts. Preferably the amount of urea (al) and/or urea-aldehyde adducts (a2) and/or of urea-triazone fertilizers (a3) is at least about 25 wt%, more preferably at least about 30 wt%. Weight percentages (wt%) are herein relative to the total weight of compounds (a)+(b)+(c).
[0058] Preferred in the context of the invention are urea (al) and/or urea-triazone fertilizers (a3), as these permit dissolving of the highest amounts of NBPT and/or DCD.
[0059] An urea-water solution is one example of a preferred way according to the invention to dissolve the urease (dl) and/or nitrification inhibitors (d2). The ratio of water to urea generally will be between about 40 wt% water to about 60 wt% urea and about 60 wt% water to about 40 wt% urea, relative to the total weight of water and urea. The preferred ratio of urea to water is about 1 : 1.
[0060] In another preferred embodiment of the invention, an urea-triazone fertilizer (a3) is used as solvent. Urea-triazone is a liquid composition that may contain an amount of water of as low as about 8 wt%.
[0061] In one embodiment of the invention an urea (al) solution in water (b) is used for dissolving the above inhibitors (like NBPT and/or DCD). In yet another embodiment of the invention, an urea-triazone fertilizer (generally having from about 5 to about 10 wt% of water is used as solvent by itself or in combination with urea. In some embodiments, both urea (al) and urea-triazone fertilizers (a3) were used as solvent. Compounds (al), (a2) and/or (a3) are preferred over UAN as the latter does not allow to dissolve the same high amounts of the above inhibitors (like NBPT and/or DCD).
[0062] Typically the amount of UAN in the additive solution (I) of the invention is less than about 20 wt%, less than about 15 wt%, less than about 10, 9, 8, 7, 6, 5, 4, 3, 2 or 1 wt%, relative to the total weight of this solution (I). Even more preferably less than about 0.5, 0.4, 0.3, 0.2 or 0.1 wt% of UAN is present in the additive solution (I) of the invention.
[0063] Depending on the urea source, the additive solution will contain about 3 wt% water or more, preferable about 4 wt% or more. If urea is used, the amount of water generally will be about 15 wt% or more, preferably about 20 wt% or more. In one embodiment, the amount of water is about 40 wt% or less, preferably about 35 wt% or less.
[0064] The additive solution further comprises one or more organic solvents (further referred to herein as "co-solvents"). The combination of dissolved urea and organic solvent is unexpectedly effective to dissolve high amounts of the inhibitors (d) in solution. The same is true for the
combination of an urea-triazone fertilizer and organic solvents. This provides significant benefits, such as the ability to produce a highly stable additive solution. This, in turn, provides significant economic benefits, because the additive solution may be stored in a stable condition for extended periods of time at room temperature, without the need to add stabilizers such as ammonium polyphosphates. The co-solvent (c) is herein different from compounds (a) and also different from (b) water (which is an inorganic solvent).
[0065] Co-solvents (c) for use in the additive solution of the invention are preferably chosen from one or more polar protic and/or polar non-protic solvents. Most preferred in the context of the invention are solvents that are miscible with water. Protic organic solvents that might be used include C1-C6 alcohols like methanol, ethanol, n-propanol, i-propanol, n-butanol, i-butanol; glycols like ethylene glycol, propylene glycol, glycerol; amino-alcohols like ethanolamine, di- ethanol amine and triethanol amine. Other suitable solvents are dimethylsulfonoxide,
dimethylformamide (DMF), dioxanes, triethyl phosphate and/or N-methyl-2-pyrrolidone (NMP). Non-protic polar solvents include dimethylsulfoxide (DMSO), dimethyl formamide (DMF), triethyl phosphate, dioxane and the like. Preferred organic co-solvents include ethanol, ethylene glycol, DMSO and/or dioxane. Most preferred are ethanol and/or DMSO for dissolving for increasing the solubility of the inhibitors. Ethanol can work for both NBPT and DCD. DMSO is preferred for DCD.
[0066] The amounts of inhibitors (in particular NBPT and/or DCD) throughout the invention are expressed as weight percentages (wt%) relative to the total weight of the additive solution (I).
[0067] The co-solvent (c) is preferably used in an amount from about 5 to about 60 wt%, preferably in an amount from about 10 to about 55 wt%, and more preferably from about 15 to about 50 wt%, relative to the total weight of the additive solution (I) of the invention. In preferred embodiments, their amount is below about 45 wt%, preferably below about 40 wt%.
[0068] Preferably little to no N-methyl-2-pyrrolidone (NMP) and/or polyvinylpyrrolidone (PVP) is used. Preferably the amount of NMP and PVP is less than about 10, 9, 9, 7, 6, 5, 4, 3, 2 wt%, more preferably less than about 1 wt%, more preferably less than about 0.5, 0.4, 0.3, 0.2 or 0.1 wt%. Preferably the additive solution of the invention is substantially free from NMP and PVP, as these can be health deleterious . NMP for instance is listed as teratogenic.
[0069] Solutions (I) of the invention comprise at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (dl). Compounds (dl) and (d2) herein are different from each other, otherwise they would not have been mentioned separately.
[0070] Presented in the present invention, is a solution (I) of at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), said solution comprising urea (al), an urea- aldehyde adduct (a2) and/or an urea-triazone fertilizer (a3), water (b) and, ideally, also at least one organic co- solvent (c).
[0071] More in particular there is provided a solution (I) of an urease inhibitor (dl), a nitrification inhibitor (d2), or a combination of both, wherein the solution comprises:
- urea (al) and/or an urea- aldehyde adduct (a2) and/or an urea-triazone fertilizer (a3), water (b), advantageously, also at least one organic co-solvent (c), and further at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), with compounds (dl) and (d2) advantageously being different from each other.
[0072] Even more in particular there is provided a solution (I) of an urease inhibitor (dl), a nitrification inhibitor (d2), or a combination of both, wherein the solution comprises:
- urea (al) and/or an urea-triazone fertilizer (a3), water (b), advantageously, at least one organic co- solvent (c), and further
at least one urease inhibitor (dl) and/or at least one nitrification inhibitor(d2), with compounds (dl) and (d2) advantageously being different from each other.
[0073] In any of the above, compounds (a) are usually present in an amount of at least about 20 wt%, preferably at least about 25 wt%, relative to the total weight of compounds (a)+(b)+(c). For compounds (a3) this amount can even be higher.
[0074] Usually the inhibitors (dl and/or d2) are present in an amount of from about 0.04 to about 70 wt%, from about 0.04 to about 60 wt%, from about 0.04 to about 50 wt%, from about 0.04 to about 40 wt%, relative to the total weight of the solution (I), preferably in an amount of from about 0.1 to about 30 wt%. Preferably the amount of inhibitors (dl and/or d2) in said solution (I) is at least about 1 wt%, more preferably at least about 2 wt%, at least about 2.5 wt%,
at least about 3 wt%, at least about 3.5 wt%, at least about 4 wt%, at least about 4.5 wt%, more preferably at least about 5 wt%. Even more preferably, their amount is at least about 6, 7, 8, 9 or 10 wt%, relative to the total weight of the solution (I). More information on preferred amounts for the different compounds infra.
[0075] Such solutions with possibly relative high amounts of nitrification and/or urease inhibitors are named hereinafter "additive solutions". They can also be referred to as "inhibitor compositions" or "inhibitor solutions". Preferred in the context of the invention are "water based" solutions. In a preferred embodiment of the invention the additive solutions (I) of the invention are in the form of "concentrates" that can be added easily to liquid fertilizers (II). In a preferred embodiment of the invention, the liquid fertilizer (II) is provided in the form of a stock solution, meaning that in general water or another aqueous medium is added to become a final liquid fertilizer.
[0076] In additive solutions (I) of the invention, the inhibitors in question usually are present in an amount of at least about 5, 6, 7, 8, 9 wt%, preferably at least about 10, 11, 12, 13, 14 wt%, or even more preferably at least about 15, 16, 17, 18, 19 wt%, relative to the total weight of the additive solution (I). Even amounts up to about 20 wt%, up to about 25 wt%, up to about 30 wt% and more, or even up to about 40 wt% and more are achievable.
[0077] The urease inhibitors (dl) like NBPT usually are present in an amount from about 0.04 to about 40 wt% in the additive solution, preferably this amount is from about 0.1 to about 30 wt%, and more preferably this amount is from about 0.25 to about 30 wt%. Suitable amounts include for example at least about 1 wt%, preferably at least about 2 wt%, more preferably at least about 3 wt%, and even more preferably at least about 5 wt%. Preferred though are concentrates that comprise at least about 10 wt%, at least about 15 wt%, at least about 20 wt%, at least about 25 wt% up to about 30 wt% or more of urease inhibitors such as NBPT.
[0078] The nitrification inhibitors (d2) like DCD preferably are present in amount from about 0.1 to about 40 wt% in the additive solution, more preferably the amount is from about 0.1 to about 30 wt%. Suitable amounts include for example at least about 0.1 wt%, at least about 2 wt%, at least about 3 wt%, or at least about 5 wt%. Preferred though are concentrates that
comprise at least about 10 wt%, at least about 15 wt%, at least about 20 wt%, at least about 25 wt% up to at least about 30 wt% or more of nitrification inhibitors such as DCD.
[0079] An embodiment of the invention relates to an additive solution (I) of at least one urease inhibitor (dl), or a combination of at least one urease inhibitor (dl) and at least one nitrification inhibitor (d2), wherein the solution comprises:
- urea (al) and/or urea-triazone fertilizers (a3), water (b) and at least one organic co- solvent (c), and further
- at least one urease inhibitor (dl), and optionally also at least one nitrification inhibitor
(d2),
wherein compounds (a) are present in an amount of at least about 20 wt%, relative to the total weight of compounds (a)+(b)+(c), and
wherein compounds (dl) are present in amount of at least about 0.04 wt%, preferably at least about 1 wt%, more preferably at least about 2 wt%, at least about 3 wt%, relative to the total weight of the solution (I), and
wherein compounds (dl) and (d2) advantageously are different from each other.
[0080] Another embodiment of the invention relates to an additive solution (I) of at least one nitrification inhibitor (d2), or a combination of at least one nitrification inhibitor (d2) and at least one urease inhibitor (dl), wherein the solution comprises:
- urea (al) and/or urea-triazone fertilizers (a3), water (b) and at least one organic co- solvent (c), and
- at least one nitrification inhibitor (d2), and optionally also at least one urease inhibitor
(dl),
wherein compounds (a) are present in an amount of at least about 20 wt%, relative to the total weight of compounds (a)+(b)+(c), and
wherein compounds (d2) are present in amount of at least about 0.1 wt%, preferably at least about 1 wt%, more preferably at least about 2 wt%, at least about 3 wt%, relative to the total weight of the solution (I), and
wherein compounds (dl) and (d2) advantageously are different from each other.
[0081] More typical amounts for compounds (a), compounds (dl) and compounds (d2) are given above. Typical amounts for the other compounds you find below.
[0082] Urease inhibitors (dl) (in any of the above) are generally chosen from the group of: hydroxyurea, a-hydroxyketone, triketone oximes, hydroquinone (HQ), nitrapyrin and/or phosphoric triamide type inhibitors. Preferred are phosphoric triamide type inhibitors. Preferred urease inhibitors includes phosphoric triamide type inhibitors, preferred are thiophosphoric triamides, more preferred aliphatic thiophosphoric triamides. Particularly preferred are N-alkyl and/or N-acyl thiophosphoric triamides. Examples thereof are N-( n-Propyl)-thiophosphoric triamid (NPPT) and/or N-(n-butyl)-thiophosphoric triamide (NBPT). Most preferred is NBPT due to its proven activity. In a particular embodiment of the invention the urease inhibitor present in the additive solution is NPBT, used alone or in combination with one or more other urease inhibitors. Herein, compound (dl) advantageously are different from compounds (d2).
[0083] Nitrification inhibitors (d2) (in any of the above) are generally chosen from the group of: dicyandiamide (DCD), 3,4-dimethylpyrazzole phosphate (DMPP), 2-chloro-6- (trichloromethyl)-pyridine (N-Serve), thiourea (TU), 2-sulfanilamidothiazole, 4-amino- 1,2,1, triazole, 3 -mercapto- 1,2, 4-triazole, ammonium dithiocarbamate (ADTC), ammonium thiosulfate (ATS) and/or 3-mercapto-benzothiazole (MBT). Preferred herein are DCD, ATS, TU and/or DMPP, more preferred are DCD, ATS and/or DMPP, and most preferred is DCD due to its efficacy, besides it availability and environmental safety. In a particular embodiment of the invention the nitrification inhibitor present in the additive solution is DCD, used alone or in combination with one or more other nitrification inhibitors. Herein, compound (d2)
advantageously are different from compounds (dl).
[0084] In one embodiment of the invention the additive solution (I) comprises NBPT. In another or the same embodiment, the additive solution (I) comprises DCD.
[0085] In another embodiment of the invention the additive solution (I) comprises NBPT and no other urease and/or nitrification inhibitors. In yet another embodiment of the invention the additive solution comprises DCD and no other nitrification and/or urease inhibitors. In still yet another embodiment of the invention, the additive solution comprises both NBPT and DCD but no other nitrification and/or urease inhibitors.
[0086] The co-solvent (c) that is used in the invention can be any organic solvent that is able to dissolve the inhibitors in question (like NBPT and/or DCD) and that is miscible with water. Suitable candidates can for instance be found amongst polar protic solvents and/or polar non- protic solvents. Preferably no strong acids are used. Protic organic solvents include C1-C6 alcohols like methanol, ethanol, n-propanol, i-propanol, n-butanol, i-butanol; glycols like ethylene glycol, propylene glycol, glycerol; amino-alcohols like ethanolamine, di-ethanol amine and tri ethanol amine and the like. Non-protic polar solvents include dimethyl sulfoxide (DMSO), dimethyl formamide (DMF), triethyl phosphate, dioxane and the like.
[0087] Particularly suitable are: lower alcohols (especially C1-C6 alcohols, and in particular ethanol), glycols (like e.g., ethylene glycol), dimethylsufonoxide (DMSO), amino-alcohols, dimethylformamide (DMF), dioxanes and/or triethyl phosphate. Preferred are ethanol, glycols like ethylene glycol, DMSO, DMF and/or dioxanes. Most preferred are ethanol and/or DMSO.
[0088] C1-C6 alcohols and in particular ethanol were found suitable to dissolve high amounts of urease inhibitors like NBPT. They can be used to dissolve DCD too. Organic solvents like DMSO, dioxanes and DMF were found most suitable to dissolve high amounts of nitrification inhibitors like DCD. Particularly preferred for that purpose was DMSO.
[0089] In one embodiment of the invention the urease and/or nitrification inhibitors are dissolved in an urea solution in water supplemented with at least one co-solvent to reach high enough concentrations of the inhibitors. In another embodiment of the invention the urease and/or nitrification inhibitors are dissolved in an urea-triazone fertilizer (having e.g., about 5 to about 10 wt% of water) supplemented with at least one co-solvent to reach high enough concentrations of the inhibitors. In that case no extra addition of water is needed to prepare a solution, as there is enough water in the product. In yet another embodiment of the invention, a combination of (1) urea in water and of (2) an urea-triazone fertilizer are used to dissolve the inhibitors, and advantageously at least one co-solvent is then used to arrive at high enough concentrations.
[0090] Apart from the above, the additive solutions of the invention (any of the above) optionally may further comprise at least one of (e): dyes, colorants, odor masking agents, flow
aids, surfactants, silicas, thickeners, viscosity modifiers, pH control agents, etc. Preferred compounds (e) are dyes and/or colorants.
[0091] In an embodiment, the sum of the weight percentages of compounds
(a)+(b)+(c)+(d)+(e), when expressed relative to the total weight of the additive solution (I) equals 100 wt%. In another embodiment, the sum of the weight percentages of compounds (a)+(b)+(c)+(d), when expressed relative to the total weight of the additive solution (I) equals at least about 70 wt%, preferably at least about 80 wt%, more preferably at least about 90 wt%, and most preferably this sum adds up to 100 wt%.
[0092] Further provided in the invention is a process for preparing additive solutions according to the invention (any of the above).
[0093] Provided for instance is a process for preparing an additive solution of the invention, comprising the step of dissolving at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) in a solution comprising: urea (al) and/or an urea-triazone fertilizer (a3), water(b) and at least one co-solvent (c). In an embodiment of the invention only urease inhibitors (dl) are there. In another embodiment of the invention only one nitrification inhibitor (d2) are present. In yet another embodiment of the invention both compounds (dl) and (d2) are present in the additive solution. A preferred solvent is urea (al). In a particular embodiment of the invention one or more compounds (a3) are used as solvent. Possibly a mix of compounds (al) and (a2) is used in the process of the invention. With the process of the invention any of the earlier described additive solutions (I) of the invention can be prepared.
[0094] In one embodiment of the invention a solution of urea (al) in water (b), and at least one organic co-solvent (c) is used to dissolve the inhibitors (d). In another embodiment of the invention a solution of urea-triazone fertilizer (a3), water (a3, b), and at least one organic co- solvent (c) is used to dissolve the inhibitors (d).
[0095] If needed, then some heating is used to prepare a clear liquid solution. If the reaction is endothermic then heating till room temperature (RT, about 18 °C to about 25 °C) may suffice. In other instances a heating up to about 100 °C, more preferably up to about 90 °C may be useful.
[0096] Generally the solution is stirred for a while to become a homogeneous solution. Shear stirring can be used but is not necessary. In general solutions of the invention can be stored at temperatures from about 10 °C to about 40 °C (in particular at RT) for about 6 months, even up to 1 year without phase separation.
[0097] Optionally, one or more of the following compounds may be included in the additive solution of the invention: dye, colorant, odor masking agent, flow aid, surfactant, silica, thickener, viscosity modifier, pH control agent, etc (compounds e). An advantage of the invention is that even without surfactants and pH control agents a clear and stable solution can be obtained.
[0098] Provided in the invention are also additive solutions that can be obtained via the above process(es).
[0099] An advantage of additive solutions (I) of the invention is also that they are stable at room temperature (RT) for longer periods, without the need for stabilizers like ammonium polyphosphates. Usually less than about 0.5 wt%, preferably less than about 0.4 wt% of ammonium polyphosphates are present in additive solutions of the invention. In a specific embodiment of the invention no ammonium polyphosphates are present in additive solutions of the invention.
[00100] Additive solutions of the invention were found to mix well with liquid fertilizers well known in the art.
[00101] Provided in the invention is for instance a process for preparing a liquid fertilizer (II) having at least urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), comprising the step of adding an additive solution (I) of the invention (any of the above) to a sulfur containing liquid fertilizer (II). For instance DCD containing additive solutions of the invention were found compatible with thiosulfate fertilizers like ammonium thiosulfate.
[00102] Further provided in the invention is a process for preparing a liquid fertilizer (II) having at least one nitrification inhibitor (dl) and/or at least one urease inhibitor (d2), comprising the step of adding an additive solution (I) of the invention (any of the above) to a nitrogen containing liquid fertilizer (II). The nitrogen containing liquid fertilizer herein advantageously is different
from compounds (d; dl and/or d2). A preferred nitrogen fertilizer is one that comprises urea, more in particular urea and ammonium nitrate (like UAN, preferably UAN 28-32). Another example is liquid urea.
[00103] The nitrogen fertilizer can further comprise a sulfur containing fertilizer too. The sulfur containing fertilizer in general is chosen from polysulfides, (bi)sulfite and/or thiosulfate fertilizers. By "(bi)sulfite" is meant sulfite, bisulfite or a mixture of both. The sulfur containing liquid fertilizer herein advantageously is different from compounds (d; dl and/or d2).
[00104] Preferably the urease inhibitors (dl) are present in the liquid fertilizer in an amount of from about 0.04 to about 5 wt%, and preferably the nitrification inhibitors (d2) are present in the liquid fertilizer in an amount of from about 0.5 to about 10 wt%, this relative to the total weight of the liquid fertilizer.
[00105] The preferred concentration of NBPT in the liquid fertilizer (II) is from about 0.04 to about 2 wt%, preferably from about 0.04 to about 1.5 wt%. Preferably the amount of NBPT herein is at least about 0.05 wt%, at least about 0.06 wt%.
[00106] The preferred end concentration for DCD in the liquid fertilizer (II) is from about 0.2 to about 5 wt%, preferably from about 1 to about 2 wt%.
[00107] When both urease inhibitors and nitrification inhibitors are present then they are generally present in a ratio of between 1 : 10 to 6: 10, preferably 2: 10 to 3 : 10. Provided in the invention are any liquid fertilizers that can be obtained via the process(es) here described.
[00108] The present invention furthermore provides for liquid "concentrated" nitrogen based fertilizers (II), preferably comprising urea, and more preferably comprising urea and ammonium nitrate, to which an additive solution of the present invention (any of the above) is added.
Possibly an additive solution having up to about 30 wt% NBPT and an additive solution having up to about 30 wt% DCD (possibly with an urea-triazone fertilizer (a3) as solvent instead of an urea solution in water) are both prepared, where after at least one of them, possibly both, are added to a stock solution of a liquid fertilizer (II), for example a stock solution comprising an UAN fertilizer, or a stock solution comprising an UAN fertilizer combined with a thiosulfate liquid fertilizer.
[00109] In one embodiment, it is preferred to prepare an additive solution of urea in water and a co-solvent with up to about 30 wt% NBPT and another one with up to about 30 wt% DCD (possibly with an urea-triazone fertilizer (a3) as solvent instead of an urea solution in water), and combine the required amounts of NBPT and/or DCD solutions with a stock solution of a liquid fertilizer (II), for example one comprising an UAN fertilizer, or an UAN fertilizer combined with a thiosulfate liquid fertilizer (II).
[00110] In another embodiment, it is preferred to prepare an additive solution of urea in water and optionally a co-solvent with up to about 30 wt% NBPT and another one with up to about 30 wt% DCD (possibly with urea-triazone fertilizer as solvent instead of an urea solution in water), and combine the required amounts of NBPT and/or DCD solutions with a stock solution of a liquid sulfur containing fertilizer, for instance a thiosulfate liquid fertilizer to which, optionally, an UAN fertilizer is added. This is suitable in particular for use with one or more DCD-based additive solutions of the invention, possibly one containing DCD and NBPT.
[00111] In yet another embodiment, it is preferred to prepare an additive solution of urea in water and optionally a co-solvent with up to about 30 wt% NBPT and another one with up to about 30 wt% DCD (possibly with urea-triazone fertilizer as solvent instead of an urea solution in water), and combine the required amounts of NBPT and/or DCD solutions with a stock solution of a mixed N-S fertilizer (III), comprising e.g., both an UAN fertilizer and a thiosulfate liquid fertilizer.
[00112] In any of the above, it is possible to use one stock solution having both NBPT and DCD, instead of using 2 separate stock solutions ("additive solutions").
[00113] The invention further provides for additive solutions (I) obtainable according to any of the processes described herein and for liquid fertilizers (II) or (III) obtainable according to any of the processes described herein.
[00114] Additive solutions (I) of the invention are in particular suitable for the making of liquid mixed N-S fertilizers (III).
[00115] Provided in the invention is hence a liquid mixed N-S fertilizer (III) composition comprising:
water,
a sulfur containing fertilizer (SF1), selected for instance from polysulfide, (bi)sulfite and/or thiosulfate fertilizers,
a nitrogen containing fertilizer (NF2), more in particular an urea based nitrogenous fertilizer, and
at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) (like NBPT and/or DCD),
wherein compounds (dl) advantageously are different from compounds (d2),
wherein the amount of S is more than about 2 wt%, preferably more than about 5 wt%, relative to the total weight of the fertilizer (III), and
wherein the amount of N is more than about 5 wt%, preferably more than about 20 wt%, and more preferably more than about 25 wt% relative to the total weight of the fertilizer (III) .
[00116] Such liquid mixed fertilizer (III) can be prepared from one or more additive solutions (I) of the invention (any of those described heretofore).
[00117] Preferred sulfur containing fertilizers are thiosulfates, and more in particular Me- thiosulfates, wherein "Me" is (NH4)2, K2, Ca, Mg, Mn, Zn, Cu and/or Fe. "Me" preferably is (NH4)2, K2, Ca, Mg and/or Mn. Preferred are (NH4)2, K2, Ca and/or Mg. Most preferred is (NH4)2. Often the thiosulfates are provided in the form of an aqueous solution having > 4 wt% Me-thiosulfate (on solids); preferably more than about 5 wt%, more preferably more than about 10 wt%. Advantageously the thiosulfates are different from compounds (d). Advantageously, the sulfur containing fertilizer (SF1) added is different from compounds (d).
[00118] Preferred nitrogen containing fertilizers are urea based fertilizers that can be urea, UAN, N-sure (urea-triazone), urea-methylene etc. Preferred are nitrogenous fertilizers that contain urea and ammonium nitrate, like UAN. In the mixed liquid N-S fertilizer (III) at least one urease inhibitor and/or at least one nitrification inhibitor are present.
[00119] Preferred for use in the context of the present invention are liquid N and/or liquid S fertilizers. In a preferred embodiment of the invention, both the sulfur containing fertilizer (SF1) and the nitrogen containing fertilizer (NF2) are liquid fertilizers. They can be added as separate fertilizers, or can be provided under the form of a single liquid N-S fertilizer to which then at
least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) (like NBPT and/or DCD) are then added.
[00120] In another embodiment of the invention, part of the fertilizers can be solid in nature. For instance, a solid urea ammonium sulfate (like e.g., a 33-0-0-12S fertilizer) can be added to or be present in the liquid mixed N-S fertilizer (III) of the invention.
[00121] The urease inhibitor preferably is NBPT and the nitrification preferably is DCD. If NBPT is present, then often in a concentration of more than about 0.04 wt%, more preferably more than about 0.1 wt%, relative to the total weight of the mixed liquid fertilizer (III). If DCD is present, then often in a concentration more than about 0.04 wt%, preferably more than about 0.1 wt%, and more preferably more than about 0.2 wt%, relative to the total weight of the mixed liquid fertilizer (III).
[00122] In an embodiment of the invention, NBPT is present, either alone or with DCD. In another embodiment of the invention, DCD is present, either alone or with NBPT.
[00123] In a particular embodiment of the invention both NBPT and DCD are present in the mixed N-S liquid fertilizer (III) as described herein. In that case the preferred ratio of NBPT to DCD is from 0.1 : 1 to 10: 1; preferred is a ratio of from 0.1 : 1 to 1 : 1, an example of a possible ratio is about 0.25: 1.
[00124] The claimed N-S fertilizers of the invention can be prepared avoiding the use of expensive or hazardous solvents such as DMF, NMP, etc. In fact they can be prepared using environmentally friendly solvents for delivery of the inhibitors (d), such as urea solutions or urea based compounds. Using materials of the invention it is possible to deliver these additives (compounds d) in aqueous N-S fertilizers. NBPT for instance is not easy to dissolve in an aqueous solution any may present stability issues with some of the standard liquid fertilizers. Materials of the invention help reduce this incompatibility. In fact, solutions (I) of the invention proved very stable and led to stable end fertilizers, in particular stable N-S fertilizers.
[00125] The presence of compounds (a) increases the stability of compounds (d) delivered. The presence of the co-solvent(s) (c) allows the delivery of compounds (d) over whatever
concentration range wanted and allows to further reduce of noxious and expensive organic
solvents. The use of stock solutions (I) of the invention brings the necessary flexibility to the end user, they are easy to handle and friendly to man and the environment.
[00126] The mixing, adding of the required amounts of inhibitors from one or more additive solutions (I) of the invention can be done at the level of the liquid fertilizer producer or the distributor. In that respect, another aspect of the invention relates to a container tank holding one or more of the above described fertilizer compositions. The container tank can be holding tank. Alternatively, the liquid fertilizers (II) or (III) herein described (any of those described) can be pumped to tanker trucks for distribution.
[00127] Alternatively, the mixing can be done at the level of the end user, just before use. In that respect, another aspect of the invention relates to a kit-in-parts containing: at least one additive solution (I) of the invention, optionally containing a dye
at least one liquid sulfur containing fertilizer (any of those described), optionally containing a different dye, and,
optionally, a sheet or card with dosage recommendations.
[00128] Preferably the liquid sulfur containing fertilizer is a liquid thiosulfate fertilizer, most preferably is a stock solution of a liquid thiosulfate fertilizer.
[00129] Liquid fertilizers (II) or (III) as described herein preferably contain from about 28 to about 32 wt% of nitrogen. Preferred is an amount of about 28 wt% of total nitrogen. In another or the same embodiment, liquid fertilizers (II) or (III) as described herein preferably contain from about 1 to about 10 wt% of sulfur, preferably they contain about 5 wt% of total sulfur.
[00130] Yet another aspect of the invention relates to the use of one or more additive solutions (I) of the invention for the making of an 28-0-0-5 S fertilizer.
[00131] In any of the embodiments described herein the most preferred urease inhibitor is NBPT and the most preferred nitrification inhibitor is DCD.
[00132] In a preferred embodiment the ratio of water : urea : co-solvent is about 1 : 1 : 1. In another preferred embodiment the ratio of water : urea : co-solvent is about 1 : 1 :2. This means
that in additive solutions (I) of the invention far less organic solvents are used compared to solutions in organic solvents that are on the market. And if e.g., ethanol is used as co-solvent then carcinogenic solvents like DMSO can be avoided. The use of ethanol (used in relatively small amounts) further has the advantage that the additive solution obtained is not flammable.
[00133] When an urea-triazone fertilizer (a3) is used as solvent instead of the urea in water solution then extra water can be added, but this is not necessary as this type of fertilizer in general is a liquid product. Additive solutions of this type were particularly suitable to dissolve up to about 15 wt% and more, preferably from about 20 wt% and more of DCD.
[00134] In case the urease and nitrification inhibitors are combined in one solution, it is preferred to use relative amounts according their required activity, but other relative amounts can be used. Suitable amounts are 10: 1 to 1 :20, preferably 1 : 1 to 1 : 10, like for example about 1 :2 for NBPT to DCD, preferably about 1 :4 for NBPT to DCD. More preferred ratios of the urease inhibitor to nitrification inhibitor given as ratio of NBPT to DCD is between 1 : 10 to 6: 10, more preferably between 2: 10 to 3: 10.
[00135] The additive solution may further comprise further components like for example odor masking agents, colorants, dyes, pH control agents, flow aids, surfactants, and combinations thereof (compounds e).
[00136] The odor of the compositions of the present invention is anyhow relatively low, in comparison to the whole-organic solvent solutions of the prior art. Nevertheless, it can be useful to add such a component, in particular if the additive has further useful properties, like for example also lowering the salt out temperature.
[00137] A preferred odor masking agent includes one of isoamyl butyrate, 4-allylanisole, limonene, terpineol, terpenes, 4-(2, 6, 6-trimethyl -2-cyclo-hex enyl)-3-buten-2-one, benzaldehyde, diethyl malonate, cyclohexyl acetate, anisole, a-ionone, mint oil, Japanese cherry and rose ketones.
[00138] Generally, the additive solution comprises an amount of less than about 5 wt% (by total weight of composition) of odor masking agent, preferably, less than about 3 wt%. Preferably, the additive solution comprises an amount of from about 1 wt% to about 3 wt% of the odor masking
agent (for example, isoamyl butyrate). The odor masking agent preferably lowers the salt-out temperature of the composition
[00139] In one embodiment, a dye or colorant is present in the additive solution at an amount of about 0.05 wt% or higher, preferably about 0.1 wt%, or higher (wt% relative to the total composition). Preferred are dyes and more in particular food grade dyes. The dye - if present - generally is present in the composition in an amount of about 3 wt% or lower, preferably about 1 wt% or lower. Suitable examples include yellow, blue, red and/or green food grade dyes.
[00140] As pH control agents, acid, base or buffering compounds can be used. If required, suitably, an acidic compound can be included as a pH control agent to maintain or to adjust the pH of the additive solution. Illustrative acids can include, but are not limited to, mineral acids such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, acetic acid, ammonium bisulfite (ABS) or any combination thereof. If required, suitably a basic compound can be included as a pH control agent to maintain or to adjust the pH of the additive solution. Illustrative base compounds for adjusting the pH can include, but are not limited to, ammonia, amines, e.g., primary, secondary, and tertiary amines and polyamines, sodium hydroxide (NaOH), potassium hydroxide (KOH), or a combination thereof. Other Illustrative pH buffering compounds are for instance triethanolamine, sodium borate, potassium bicarbonate, sodium carbonate, potassium carbonate, or any combination thereof.
[00141] The additive solution (I) can be mixed with dissolved fertilizers. Fertilizers are common water soluble inorganic fertilizers that provide nitrogen, and optionally further nutrients such as phosphorus, potassium, sulfur and other nutrients. Examples of such fertilizers include: for nitrogen as the nutrient: urea, urea-aldehyde oligomers, nitrates and or ammonium salts such as ammonium nitrate, including in combination with urea e.g., as UAN type materials, calcium ammonium nitrate, ammonium sulfate nitrate, ammonium phosphates, like mono-ammonium phosphate, di -ammonium phosphate and ammonium polyphosphate, ammonium sulfate, ammonium thiosulfate, and the like. It is understood that a fertilizer composition can comprise one or a combination of the fertilizers described herein.
[00142] Preferred nitrogenous fertilizers are those containing a nitrogenous compound such as urea, urea-aldehyde oligomers, nitrate salts, ammonium salt, or a mixture thereof, such as
ammonium nitrate, ammonium sulfate, ammonium thiosulfate, ammonium polysulfide, ammonium phosphates, ammonium chloride, ammonium bicarbonate, ammonia, calcium nitrate, nitrate soda, calcium cyanamide.
[00143] Preferably, the nitrogenous fertilizer comprises urea (often about 1% to about 23% N solutions), or urea and ammonium nitrate (UAN). Suitable urea and ammonium nitrate- containing fertilizers include, for example, UAN 18, UAN 28, UAN 30 and UAN 32, triazone, urea methylene, urea-aldehyde adducts and the like.
[00144] Preferred UAN concentrates include UAN 18, UAN 28, UAN 30, UAN 32, and more preferred UAN concentrates are UAN 28 or UAN 32, UAN 32 being most preferred. Preferred urea (often about 2% to about 20% N solutions) and urea adducts include N-sure, an urea- triazone fertilizer and Trisert® triazone fertilizers (often about 5% to about 25% N solutions).
[00145] In one embodiment of the invention, the urea based fertilizer solution further comprises a sulfur containing fertilizer. Suitable sulfur containing fertilizers include polysulfide, (bi)sulfite and/or thiosulfate salts. Preferred polysulfide salts include calcium polysulfide (sold for instance under the name Solmenda® (formerly Soil-Mend™), Sulforix® or Rex Lime Sulfur) more preferred sulfur containing fertilizer salts include (bi)sulfite and thiosulfates. Suitable (bi)sulfite based liquid fertilizer, include K-ROW 23® (potassium sulfite) and ammonium bisulfite. Sulfite components like sodium sulfite have been described as urease inhibitors. The inhibitor is believed to bind to the di -nuclear Ni(II) center of some bacterial urease in a tridentate mode involving bonds between the two Ni(II) ions in the active site and all three oxygen atoms of the inhibitor.
[00146] Most preferred thiosulfate salts include Me thiosulfate, wherein Me is ammonium, potassium, calcium, magnesium, manganese, zinc, copper and/or iron. Preferred Me ions include ammonium, potassium, calcium and/or magnesium. In one embodiment, ammonium thiosulfate is used, because of its additional stabilizing effect on urea. Thiosulfate based liquid fertilizers are well known, and comprise for example:
Ammonium thiosulfate (Thio-Sul®), which is a 50-60% aqueous solution, (grade is 12-
0-0-26).
Potassium thiosulfate (KTS®), which is a 50% aqueous solution, (grade is 0-0-25-17S). Calcium thiosulfate (CaTs®), which is a 24-25% aqueous solution, (grade is 0-0-0-10S-
6Ca)
Magnesium thiosulfate (MagThio®), which is a 24-25% solution, (grade is 0-0-0- 10S-
4Mg)
[00147] In one embodiment, a concentrated fertilizer composition is made by combining the inhibitor composition (additive solution) of the present invention with a concentrated
nitrogenous fertilizer to form a concentrated liquid nitrification-inhibited fertilizer composition.
[00148] In a further embodiment of the invention, a diluted fertilizer composition is prepared by subsequently diluting the concentrated liquid nitrification-inhibited fertilizer composition with an aqueous medium, preferably water in a ratio of up to about 500 pbw, more preferably from about 10 to about 500 pbw and even more preferably from about 100 to about 300 pbw, of the aqueous medium per about 1 pbw concentrated liquid nitrogenous fertilizer composition.
[00149] In one embodiment, the end use fertilizer composition of the present invention is made by combining the additive solution(s) (I) of the present invention, a concentrated liquid nitrogenous fertilizer, and an aqueous medium.
[00150] In one embodiment, the end use fertilizer composition of the present invention comprises one or more urease inhibitors, preferably NBPT, alone or in combination with one or more nitrification inhibitors.
[00151] In one embodiment, the end use fertilizer composition (II) of the present invention comprises from about 0.001 to about 5 pbw, preferably from about 0.01 to about 2 pbw urease inhibitor and/or nitrification inhibitor per about 100 pbw of the one or more nitrogenous fertilizer compounds.
[00152] In one embodiment, the end use fertilizer composition is applied to target plants or to an environment for the target plants, i.e., to ground on or within which the target plants are growing or to be grown, at a rate of from about 0.01 pounds to about 5 pounds of the fertilizer
composition, preferably from about 0.05 pounds to about 2 pounds of the fertilizer composition, per 1000 square feet of ground.
[00153] In one embodiment, the end use fertilizer composition is applied to target plants or to an environment for the target plants at a rate effective to provide a dosage of fertilizer of from about 0.01 pounds to about 5 pounds of fertilizer, preferably from about 0.05 pounds to about 2 pounds of fertilizer, per 1000 square feet of ground.
[00154] The composition of the present invention provides improved ease of handling of urease inhibitors and/or nitrification inhibitors, improved solubility characteristics, low toxicity of the water based solution with only a relatively low amount of organic solvents, good storage characteristics, and excellent miscibility with aqueous compositions, such as aqueous nitrogenous fertilizer formulations.
[00155] Below are listed some combinations of these products that can be made to reduce ammonia loss and slow down nitrification. The compositions are described as percent by weight on a ton basis.
[00156] Additive solutions (I) of the invention and liquid fertilizers (II) of the invention help stimulate plant growth, and reduce ammonia loss and slow down nitrification.
[00157] Below are listed some formulations of the current invention. It should be understood that any of the named formulations below are for illustration only and not limited to just these formulations but includes all known formulations that are suitable for obtaining good inhibition of urease and of nitrification. The products listed below are not limited to just these products but includes all liquid fertilizers and suspension fertilizers commonly used in the liquid fertilizer industry that would require the use of NBPT as an urease inhibitor to reduce or minimize ammonia loss or the use of DCD as a nitrification inhibitor to slow or reduce nitrification reaction in the soil.
[00158] The tables below describe a number of possible compositions. These compositions can be made by mixing concentrated additive solutions with urea and/or UAN solutions.
[00159] For UAN (urea nitrogen containing fertilizers) formulations using this technology nitrogen content can range from about 1% N as UAN1 to about 31.9% N as UAN32, preferably between about 5 and about 31.9% and more preferably between about 16 and about 31.9%. For liquid urea, nitrogen content can range about 1% to about 23%, preferably between about 5% and about 23% and more preferably between about 15 and about 20%. Ranges for liquid phosphate are from about 0.1% to about 33.9% while ranges for potassium are from about 0.1% to about 24.9% using potassium thiosulfate and from about 0.1% to about 22.9% using potassium bi/sulfite. Ranges for NBPT are from about 0.01% to about 5%, for DCD from about 0.1 to about 20% and for Thio-Sul from about 1.0% to about 25.9% sulfur. Other nutrients and micronutrients that can be added include zinc, boron, calcium, iron, copper, molybdenum, manganese, and magnesium.
[00160] Examples of potential blends with UAN32, NBPT, Ammonium thiosulfate (ATS) and DCD:
[00161] Examples of UAN32, Potassium thiosulfate (KTS®), Ammonium polyphosphate (APP), NBPT and DCD:
[00162] Examples of UAN32, Calcium thiosulfate (CaTs®), NBPT and DCD:
[00165] Preferred compositions are relatively high strength compositions, and particularly preferred are high strength compositions with a relatively high amount of sulfur.
[00166] The invention will be elucidated with the following examples, without being limited thereto.
[00167] EXAMPLES [00168] Examples 1-8
Urea is dissolved in the same amount of water by stirring. Thereafter - if applicable - the co- solvent is mixed, and thereafter the urease and/or nitrification inhibitor. The amounts are given in the Table below.
*N-Sure® (an urea-triazone fertilizer) contains about 8% water; hence, of the 20 wt% about 1.6 wt% is water.
** Strength (wt% on the total weight of a+b+c)
*** Strength (wt% on the total of the additive solution I)
[00169] The resulting solutions are clear to the eye. The solutions are storage stable at temperatures between about 15 °C and about 40 °C. The solution can be used to add a required amount of NBPT and/or DCD to a liquid fertilizer as wanted.
[00170] Example 9
[00171] To prepare a liquid fertilizer with the composition 20-0-0-3 S plus NBPT and DCD (from urea and ammonium thiosulfate), 197.6 grams urea, 52.4 grams ammonium thiosulfate, 199.46 grams water, 0.99 grams NBPT, 3.95 grams DCD were mixed and stirred to dissolve.
[00172] Example 10
[00173] As an alternative to Example 9, a stock solution of 10 kg urea and 10 L of water 10 kg of ethanol with 5 kg DCD and 1.25 kg NBPT was prepared by stirring first water and urea, adding ethanol and thereafter adding DCD and NBPT and further stirring, till a clear solution was obtained.
[00174] A solution of 187.6 kg urea, 52.4 kg ammonium thiosulfate and 189.46 kg water was prepared. To this mixture, the 25 kg of stock solution was added. The resulting solution was clear and storage stable.
[00175] Example 11
[00176] In yet another example according to the invention, 30 grams of an urea-triazone fertilizer (N-Sure®, about 8 wt% is water) was mixed with 15 grams of DMSO to form a homogeneous solution. To this, 15 grams of DCD was added and the mixture was heated to 85° C to dissolve the DCD with stirring. The resulting 25% DCD solution (15 grams DCD/60 grams total weight - 25 wt%) was cooled to ambient and packed as such.
[00177] Example 12
[00178] In yet another example according to the invention, 100 grams of Ethanol, 100 grams of urea-triazone fertilizer (N-Sure®), 100 grams of 50% urea in water solution and 130 grams of NBPT were mixed and heated to about 45°C until dissolved. The resulting 30% NBPT solution (130 grams NBPT/430 grams total weight Ά >30 wt%) was cooled to ambient and packaged as such.
[00179] Packaged, the additive solutions (I) of the invention could be stored for several months, even up to 1 year without phase separation and/or precipitation. An additive solution according to the invention, containing about 20 wt% of NBPT in urea/ethanol, was subjected to a HPLC method to see if the NBPT had remained stable. Gradient HPLC was used for these purposes. Were used herein: a propylamine column, a Diode Array Detector set at 2014 nm, and acetonitrile : water as mobile phase. The gradient table is the one below:
[00180] Gradient Table:
[00181] In one year time, the NBPT had lost less than 4% of its activity. Additive solutions (I) of the invention are thus both chemically and physically stable when stored in closed containers under normal conditions of pressure and temperature (about 1 bar, about l8-25°C). This is surprising, as water was thought to facilitate the decomposition of NBPT into a non-effective substance. Without being bound by theory, it is believed that compounds (a) protect compounds (d) from destabilization, even sensitive compounds like NBPT.
Claims
1. An additive solution (I) of at least one urease inhibitor (dl) and/or at least one
nitrification inhibitor (d2), said solution comprising:
- urea (al) and/or an urea-aldehyde adduct (a2) and/or an urea-triazone fertilizer (a3), water (b), at least one organic co-solvent (c), and further
- at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), wherein compounds (a) are present in an amount of at least 20 wt%, preferably at least 25 wt%, relative to the total weight of compounds (a)+(b)+(c),
wherein compounds (dl) and (d2) are different from each other, and
wherein compounds (d) are present in an amount of at least 2.5 wt%, at least 3 wt%, preferably at least 5 wt%, relative to the total weight of the additive solution (I).
2. The additive solution according to claim 1, comprising:
- urea (al) and/or an urea-triazone fertilizer (a3), water (b), at least one organic co-solvent (c), and further
- at least one urease inhibitor (dl), or a combination of at least one urease inhibitor (dl) and at least one nitrification inhibitor (d2),
wherein the amount of urease inhibitors (dl) is at least 1 wt%, preferably at least 2 wt%, more preferably at least 3 wt%, relative to the total weight of the additive solution (I).
3. The additive solution according to claim 1 comprising:
- urea (al) and/or an urea-triazone fertilizer (a3), water (b), at least one organic co-solvent (c), and further
- at least one nitrification inhibitor (d2), or a combination of at least one nitrification (d2) inhibitor and at least one urease inhibitor (dl),
wherein the amount of nitrification inhibitors (d2) is at least 0.1 wt%, preferably at least 1 wt%, more preferably at least 2 wt%, relative to the total weight of the additive solution (I).
4. The additive solution according to any one of claims 1-3, wherein urease inhibitors (dl) are present in an amount of at least 5 wt%, preferably at least 15 wt%, up to 30 wt% and more, and/or wherein nitrification inhibitors (d2) are present in an amount of at least 5 wt%, preferably at least 15 wt%, up to 30 wt% and more, relative to the total weight of the additive solution (I).
5. The additive solution according to any one of claims 1-4, wherein compounds (d) are present in an amount up to 40 wt%.
6. The additive solution according to any one of claims 1-5 wherein the urease inhibitor (dl) is a phosphoric triamide type inhibitor, preferably a thiophosphoric triamide type inhibitor.
7. The additive solution according to any one of claims 1-6 wherein the nitrification inhibitor (d2) is dicyandiamide (DCD), ammonium thiosulfate (ATS), thiourea (TU) and/or dimethylpyrazzole phosphate (DMPP), preferably DCD, ATS and/or DMPP.
8. The additive solution according to any one of claims 1-7, wherein the co-solvent is a polar protic and/or a polar non-protic solvent that is miscible with water, such as ethanol, ethylene glycol, DMSO and/or dioxane.
9. The additive solution according to any one of claims 1-8 further containing (e) at least one dye and/or colorant.
10. A process for preparing an additive solution (I) according to any one of claims 1-9, comprising the step of dissolving at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2) in a solution comprising: (a) urea (al) and/or an urea-aldehyde adduct (a2) and/or an urea-triazone fertilizer (a3), (b) water and at (c) least one organic co-solvent that preferably is selected from polar protic and/or polar non-protic solvents that are miscible with water.
11. The process according to claim 10 wherein some heating is used to prepare a clear liquid solution.
12. A process for preparing a liquid fertilizer (II) having at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), comprising the step of adding to a liquid fertilizer at least one additive solution (I) according to any one of claims 1-9.
13. The process of claim 12 wherein the liquid fertilizer comprises a nitrogen containing fertilizer, preferably a liquid nitrogen containing fertilizer that can be provided in the form of a stock solution that still has to be diluted with water.
14. The process of any one of claims 12-13, wherein the liquid fertilizer comprises a sulfur containing fertilizer, the sulfur containing fertilizer preferably being chosen from polysulfides, (bi)sulfites and/or from thiosulfate fertilizers, wherein the sulfur containing fertilizer
advantageously is different from compounds (d).
15. The process according to any one of claims 12-14 wherein urease inhibitors (dl) are present in an amount of from 0.5-10 wt% and/or wherein nitrification inhibitors (d2) are present in an amount of from 1-5 wt%, relative to the total weight of the liquid fertilizer (II).
16. The process according to any one of claims 12-15, wherein both urease inhibitors (dl) and nitrification inhibitors (d2) are present and this in a ratio of from 1 : 10 to 6: 10, preferably from 2: 10 to 3:10.
17. The process according to any of claims 12-16 further comprising the step of diluting the fertilizer by the addition of an aqueous medium, preferably water.
18. A liquid mixed N-S fertilizer composition (III) comprising:
water,
a sulfur containing fertilizer, selected for instance from polysulfide, (bi)sulfite and/or thiosulfate fertilizers,
a nitrogen containing fertilizer, more in particular an urea based nitrogenous fertilizer, and
at least one urease inhibitor (dl) and/or at least one nitrification inhibitor (d2), wherein compounds (dl) and (d2) are different from each other, and wherein the sulfur containing fertilizer advantageously is different from compounds (d),
wherein the amount of S is more than 2 wt%, preferably more than 5 wt%, relative to the total weight of the fertilizer (III), and
wherein the amount of N is more than 5 wt%, preferably more than 20 wt%, and more preferably more than 25 wt%, relative to the total weight of the fertilizer (III) and
wherein the amount of compounds (d) in said composition (III) is at least 0.04 wt%.
19. The liquid N-S fertilizer of claim 18, wherein the urease inhibitor (dl) is NBPT and wherein the nitrification inhibitor (d2) is DCD.
20. The liquid N-S fertilizer of any of claims 18 to 19, comprising DCD, optionally combined with NBPT.
21. The liquid N-S fertilizer of any of claims 18 to 19, comprising NPBT, optionally combined with DCD.
22. The liquid N-S fertilizer of any of claims 18 to 21, comprising at least one co-solvent (c) that is selected from one or more polar protic and/or polar non-protic solvents that are miscible with water.
23. The liquid N-S fertilizer of any of claims 18 to 22, prepared from an additive solution (I) according to any one of claims 1-9.
24. A kit-in-parts containing:
- at least one additive solution (I) according to any one of claims 1-9, optionally
containing a dye,
- at least one liquid sulfur containing fertilizer, that preferably is a stock solution of a thiosulfate fertilizer, the liquid sulfur containing fertilizer optionally containing a different dye, and,
- optionally, a sheet or a card with dosage recommendations.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862660663P | 2018-04-20 | 2018-04-20 | |
US62/660,663 | 2018-04-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2019204163A1 true WO2019204163A1 (en) | 2019-10-24 |
Family
ID=66323976
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2019/027346 WO2019204163A1 (en) | 2018-04-20 | 2019-04-12 | Liquid nitrogen fertilizer compositions and additives therefore |
Country Status (2)
Country | Link |
---|---|
AR (1) | AR114791A1 (en) |
WO (1) | WO2019204163A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114057522A (en) * | 2021-11-17 | 2022-02-18 | 中化农业(临沂)研发中心有限公司 | Biological stimulator composition containing double-effect slow-release nitrogen and preparation method thereof |
FR3113811A1 (en) | 2020-09-08 | 2022-03-11 | VALORISATION DES INNOVATIONS EN AGROFOURNITURES VEGETALES par abréviation VIA VEGETALE | Nitrogen fertilizer composition intended for root application |
Citations (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US569800A (en) | 1896-10-20 | Beer-tap | ||
US4242325A (en) | 1979-07-06 | 1980-12-30 | Morton-Norwich Products, Inc. | Phosphorotriamides as urease inhibitors |
US4462819A (en) | 1983-04-07 | 1984-07-31 | Allied Corporation | Urease inhibited urea based fertilizer compositions containing organo boron acid compounds |
EP0119495A1 (en) | 1983-03-16 | 1984-09-26 | Allied Corporation | S-aryl and S-aliphatic diamidophosphorothiolates as urease inhibitors and urease inhibited urea based fertilizer compositions |
EP0119487A1 (en) | 1983-03-16 | 1984-09-26 | Allied Corporation | Novel N-aliphatic and N,N-aliphatic phosphoric triamide urease inhibitors and urease inhibited urea based fertilizer compositions |
EP0119494A1 (en) | 1983-03-16 | 1984-09-26 | Allied Corporation | Urease inhibited urea based fertilizer compositions containing phosphorus compounds |
US4517003A (en) | 1983-06-08 | 1985-05-14 | Allied Corporation | N-acyl phosphoric triamide urease inhibitors and urease inhibited urea based fertilizer compositions |
US4517004A (en) | 1983-06-08 | 1985-05-14 | Allied Corporation | Aryl phosphoric triamide and aryl phosphorodiamidate urease and nitrification inhibitors and urease and nitrification inhibited urea and reduced nitrogen based fertilizer compositions |
US4517007A (en) | 1983-06-09 | 1985-05-14 | Allied Corporation | Phosphoroamide urease inhibitors and urease inhibited urea based fertilizer compositions |
US4517002A (en) | 1983-03-16 | 1985-05-14 | Allied Corporation | Phosphorodiamide urease inhibitors and urease inhibited urea based fertilizer compositions |
US4518413A (en) | 1983-06-06 | 1985-05-21 | Allied Corporation | Poly-phosphorodiamide urease inhibitors and urease inhibited urea based fertilizer compositions |
US4539037A (en) | 1983-03-16 | 1985-09-03 | Allied Corporation | Urease inhibited urea based fertilizer compositions containing N-aryl-N-aliphatic phosphorotriamide compounds |
US4540428A (en) | 1983-03-16 | 1985-09-10 | Allied Corporation | Phosphorotriamidate urease inhibitors and urease inhibited urea based fertilizer compositions |
GB2164640A (en) | 1984-09-19 | 1986-03-26 | H R H Sdn Bhd Highlands Resear | Coating, binding and sealant materials for fertilisers and other substances |
US4618691A (en) | 1984-06-28 | 1986-10-21 | Tennessee Valley Authority | Cyclotriphosphazatriene-derivatives |
US4824783A (en) | 1983-12-20 | 1989-04-25 | Enichem S.P.A. | Oxidized sulfur derivatives of diaminophosphinyl compounds as urease inhibitors |
WO1989003811A1 (en) | 1987-10-20 | 1989-05-05 | Exxon Chemical Patents, Inc. | Sulfonated polymer coatings for controlled fertilizer release |
EP0356755A1 (en) | 1988-08-08 | 1990-03-07 | Aglukon Spezialdünger Gmbh | Device for slow release fertilisation |
US4932991A (en) | 1988-11-03 | 1990-06-12 | Tennessee Valley Authority | Thiopyridine-N-oxides, thiopyridines, and thiopyrimidines as urease inhibitors |
US4932992A (en) | 1988-11-03 | 1990-06-12 | Tennessee Valley Authority | Dual purpose urease and nitrification inhibitors |
US4954156A (en) | 1989-01-17 | 1990-09-04 | Tennessee Valley Authority | N,N-dihalo-2-imidazolidinones and N-halo-2-oxazolidinones as urease and nitrification inhibitors |
US5024689A (en) | 1988-02-08 | 1991-06-18 | Freeport Mcmoran Resource Partners | Nitrogen fertilizer |
EP0476550A1 (en) | 1990-09-20 | 1992-03-25 | ProMineral Gesellschaft zur Verwendung von Mineralstoffen mbH | Soil additive pellets, to feed plants with nitrogen, and process for their production |
US5364438A (en) | 1993-11-12 | 1994-11-15 | Freeport-Mcmoran Resource Partners, Limited Partnership | Fluid urea-containing fertilizer |
US5435821A (en) | 1985-12-12 | 1995-07-25 | Exxon Research & Engineering Co. | Controlled release vegetation enhancement agents coated with sulfonated polymers, method of production and prcesses of use |
GB2285803A (en) | 1993-12-30 | 1995-07-26 | Norsk Hydro As | Urea - containing fertilizer |
WO1997004819A1 (en) | 1995-07-31 | 1997-02-13 | Caphco, Inc. | Novel compositions and devices for controlled release of active ingredients |
WO1997022568A1 (en) | 1995-12-19 | 1997-06-26 | Imc-Agrico Company | Improved formulation for fertilizer additive concentrate |
US5883297A (en) | 1997-01-21 | 1999-03-16 | Albemarle Corporation | Preparation and recovery of N-hydrocarbylthiophosphoric triamides or N-hydrocarbylphosphoric triamides |
US6262183B1 (en) | 1987-02-26 | 2001-07-17 | Cytec Technology Corp. | Hydroxamic acid polymers formed from primary amide polymers |
US6315807B1 (en) | 2000-03-28 | 2001-11-13 | Council Of Scientific And Industrial Research | Formulation useful as a nitrification and urease inhibitor and a method of producing the same |
EP1183220A1 (en) | 1999-04-08 | 2002-03-06 | SKW STICKSTOFFWERKE PIESTERITZ GmbH | Agents for improving the n-utilization of mineral and/or organic fertilizers that contain urea |
WO2002083697A1 (en) | 2001-04-12 | 2002-10-24 | Skw Stickstoffwerke Piesteritz Gmbh | Heterocyclically substituted (thio)phosphoric triamides |
WO2002090294A1 (en) | 2001-05-09 | 2002-11-14 | Summit-Quinphos (Nz) Limited | Sulphur coated urea particles using wet ground sulphur |
US20070157689A1 (en) | 2006-01-12 | 2007-07-12 | Agrotain International, L.L.C. | Additive containing N-(n-butyl)thiophsphoric triamide for urea-based fertilizer |
US20100206031A1 (en) | 2009-02-17 | 2010-08-19 | Whitehurst Associates, Inc. | Amino alcohol solutions of N-(n-butyl)thiophosphoric triamide (NBPT) and urea fertilizers using such solutions as urease inhibitors |
US8048189B2 (en) | 2009-02-17 | 2011-11-01 | Whitehurst Associates Inc. | Buffered amino alcohol solutions of N-(n-butyl)thiophosphoric triamide (NBPT) and urea fertilizers using such solutions as urease inhibitors |
US20140037570A1 (en) | 2012-08-02 | 2014-02-06 | Whitehurst Associates Inc. | NBPT solution for preparing urease inhibited urea fertilizers prepared from N-alkyl; N, N-alkyl; and N-alkyl-N-alkoxy amino alcohols |
WO2014028767A1 (en) | 2012-08-15 | 2014-02-20 | Koch Agronomic Services, Llc | Liquid compositions containing urease inhibitors and glycol alkyl ethers |
US20140090432A1 (en) | 2012-10-01 | 2014-04-03 | Gary David McKnight | Liquid Formulations of Urease Inhibitors for Fertilizers |
WO2014100561A1 (en) | 2012-12-20 | 2014-06-26 | Rhodia Operations | Liquid dicyandiamide and/or alkyl thiophosphoric triamide compositions and their use in agricultural applications |
US8888886B1 (en) * | 2013-08-06 | 2014-11-18 | Garnett B Whitehurst | NBPT solutions for preparing urease inhibited urea fertilizers prepared from N-substituted morpholines |
US20150174140A1 (en) | 2009-04-14 | 2015-06-25 | Laboratoire Hra Pharma | Method for on-demand contraception |
WO2016054012A1 (en) | 2014-09-30 | 2016-04-07 | Iannotta Leahann | Solvent for thiophosphoric triamide or dicyandiamide solutions, and related methods |
WO2017031186A1 (en) | 2015-08-17 | 2017-02-23 | Rhodia Operations | High temperature amine-stabilized dcd and/or alkyl thiophosphoric triamide solvent systems and use in agricultural applications |
WO2017083714A1 (en) | 2015-11-11 | 2017-05-18 | Koch Agronomic Services, Llc | Composition containing n-(n-butyl) thiophosphoric triamide adducts and reaction products |
WO2017081183A1 (en) | 2015-11-12 | 2017-05-18 | Yara International Asa | Improved urea-based blend composition and method for the manufacture thereof |
EP3210959A1 (en) * | 2016-02-24 | 2017-08-30 | YARA International ASA | Liquid urease inhibitor formulation, method of manufacturing and solid particulates comprising it |
US20180002246A1 (en) | 2016-06-29 | 2018-01-04 | Rhodia Operations | Stabilized dcd and/or alkyl thiophosphoric triamide solvent systems and use in agricultural applications |
-
2019
- 2019-04-12 WO PCT/US2019/027346 patent/WO2019204163A1/en active Application Filing
- 2019-04-17 AR ARP190101032A patent/AR114791A1/en unknown
Patent Citations (53)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US569800A (en) | 1896-10-20 | Beer-tap | ||
US4242325A (en) | 1979-07-06 | 1980-12-30 | Morton-Norwich Products, Inc. | Phosphorotriamides as urease inhibitors |
US4537614A (en) | 1983-03-16 | 1985-08-27 | Allied Corporation | S-aryl and S-aliphatic diamidophosphorothiolates as urease inhibitors and urease inhibited urea based fertilizer compositions |
EP0119495A1 (en) | 1983-03-16 | 1984-09-26 | Allied Corporation | S-aryl and S-aliphatic diamidophosphorothiolates as urease inhibitors and urease inhibited urea based fertilizer compositions |
EP0119487A1 (en) | 1983-03-16 | 1984-09-26 | Allied Corporation | Novel N-aliphatic and N,N-aliphatic phosphoric triamide urease inhibitors and urease inhibited urea based fertilizer compositions |
EP0119494A1 (en) | 1983-03-16 | 1984-09-26 | Allied Corporation | Urease inhibited urea based fertilizer compositions containing phosphorus compounds |
US4540428A (en) | 1983-03-16 | 1985-09-10 | Allied Corporation | Phosphorotriamidate urease inhibitors and urease inhibited urea based fertilizer compositions |
US4539037A (en) | 1983-03-16 | 1985-09-03 | Allied Corporation | Urease inhibited urea based fertilizer compositions containing N-aryl-N-aliphatic phosphorotriamide compounds |
US4517002A (en) | 1983-03-16 | 1985-05-14 | Allied Corporation | Phosphorodiamide urease inhibitors and urease inhibited urea based fertilizer compositions |
US4530714A (en) | 1983-03-16 | 1985-07-23 | Allied Corporation | N-aliphatic and N,N-aliphatic phosphoric triamide urease inhibitors and urease inhibited urea based fertilizer compositions |
US4462819A (en) | 1983-04-07 | 1984-07-31 | Allied Corporation | Urease inhibited urea based fertilizer compositions containing organo boron acid compounds |
US4518413A (en) | 1983-06-06 | 1985-05-21 | Allied Corporation | Poly-phosphorodiamide urease inhibitors and urease inhibited urea based fertilizer compositions |
US4517003A (en) | 1983-06-08 | 1985-05-14 | Allied Corporation | N-acyl phosphoric triamide urease inhibitors and urease inhibited urea based fertilizer compositions |
US4517004A (en) | 1983-06-08 | 1985-05-14 | Allied Corporation | Aryl phosphoric triamide and aryl phosphorodiamidate urease and nitrification inhibitors and urease and nitrification inhibited urea and reduced nitrogen based fertilizer compositions |
US4517007A (en) | 1983-06-09 | 1985-05-14 | Allied Corporation | Phosphoroamide urease inhibitors and urease inhibited urea based fertilizer compositions |
US4824783A (en) | 1983-12-20 | 1989-04-25 | Enichem S.P.A. | Oxidized sulfur derivatives of diaminophosphinyl compounds as urease inhibitors |
US4618691A (en) | 1984-06-28 | 1986-10-21 | Tennessee Valley Authority | Cyclotriphosphazatriene-derivatives |
GB2164640A (en) | 1984-09-19 | 1986-03-26 | H R H Sdn Bhd Highlands Resear | Coating, binding and sealant materials for fertilisers and other substances |
US5435821A (en) | 1985-12-12 | 1995-07-25 | Exxon Research & Engineering Co. | Controlled release vegetation enhancement agents coated with sulfonated polymers, method of production and prcesses of use |
US6262183B1 (en) | 1987-02-26 | 2001-07-17 | Cytec Technology Corp. | Hydroxamic acid polymers formed from primary amide polymers |
WO1989003811A1 (en) | 1987-10-20 | 1989-05-05 | Exxon Chemical Patents, Inc. | Sulfonated polymer coatings for controlled fertilizer release |
EP0357687A1 (en) | 1987-10-20 | 1990-03-14 | Exxon Chemical Patents Inc. | Sulfonated polymer coatings for controlled fertilizer release |
US5024689A (en) | 1988-02-08 | 1991-06-18 | Freeport Mcmoran Resource Partners | Nitrogen fertilizer |
EP0356755A1 (en) | 1988-08-08 | 1990-03-07 | Aglukon Spezialdünger Gmbh | Device for slow release fertilisation |
US4932992A (en) | 1988-11-03 | 1990-06-12 | Tennessee Valley Authority | Dual purpose urease and nitrification inhibitors |
US4932991A (en) | 1988-11-03 | 1990-06-12 | Tennessee Valley Authority | Thiopyridine-N-oxides, thiopyridines, and thiopyrimidines as urease inhibitors |
US4954156A (en) | 1989-01-17 | 1990-09-04 | Tennessee Valley Authority | N,N-dihalo-2-imidazolidinones and N-halo-2-oxazolidinones as urease and nitrification inhibitors |
EP0476550A1 (en) | 1990-09-20 | 1992-03-25 | ProMineral Gesellschaft zur Verwendung von Mineralstoffen mbH | Soil additive pellets, to feed plants with nitrogen, and process for their production |
US5364438A (en) | 1993-11-12 | 1994-11-15 | Freeport-Mcmoran Resource Partners, Limited Partnership | Fluid urea-containing fertilizer |
GB2285803A (en) | 1993-12-30 | 1995-07-26 | Norsk Hydro As | Urea - containing fertilizer |
WO1997004819A1 (en) | 1995-07-31 | 1997-02-13 | Caphco, Inc. | Novel compositions and devices for controlled release of active ingredients |
WO1997022568A1 (en) | 1995-12-19 | 1997-06-26 | Imc-Agrico Company | Improved formulation for fertilizer additive concentrate |
US5698003A (en) | 1995-12-19 | 1997-12-16 | Imc-Agrico Company | Formulation for fertilizer additive concentrate |
US5883297A (en) | 1997-01-21 | 1999-03-16 | Albemarle Corporation | Preparation and recovery of N-hydrocarbylthiophosphoric triamides or N-hydrocarbylphosphoric triamides |
EP1183220A1 (en) | 1999-04-08 | 2002-03-06 | SKW STICKSTOFFWERKE PIESTERITZ GmbH | Agents for improving the n-utilization of mineral and/or organic fertilizers that contain urea |
US6315807B1 (en) | 2000-03-28 | 2001-11-13 | Council Of Scientific And Industrial Research | Formulation useful as a nitrification and urease inhibitor and a method of producing the same |
WO2002083697A1 (en) | 2001-04-12 | 2002-10-24 | Skw Stickstoffwerke Piesteritz Gmbh | Heterocyclically substituted (thio)phosphoric triamides |
WO2002090294A1 (en) | 2001-05-09 | 2002-11-14 | Summit-Quinphos (Nz) Limited | Sulphur coated urea particles using wet ground sulphur |
US20070157689A1 (en) | 2006-01-12 | 2007-07-12 | Agrotain International, L.L.C. | Additive containing N-(n-butyl)thiophsphoric triamide for urea-based fertilizer |
US8048189B2 (en) | 2009-02-17 | 2011-11-01 | Whitehurst Associates Inc. | Buffered amino alcohol solutions of N-(n-butyl)thiophosphoric triamide (NBPT) and urea fertilizers using such solutions as urease inhibitors |
US20100206031A1 (en) | 2009-02-17 | 2010-08-19 | Whitehurst Associates, Inc. | Amino alcohol solutions of N-(n-butyl)thiophosphoric triamide (NBPT) and urea fertilizers using such solutions as urease inhibitors |
US20150174140A1 (en) | 2009-04-14 | 2015-06-25 | Laboratoire Hra Pharma | Method for on-demand contraception |
US20140037570A1 (en) | 2012-08-02 | 2014-02-06 | Whitehurst Associates Inc. | NBPT solution for preparing urease inhibited urea fertilizers prepared from N-alkyl; N, N-alkyl; and N-alkyl-N-alkoxy amino alcohols |
WO2014028767A1 (en) | 2012-08-15 | 2014-02-20 | Koch Agronomic Services, Llc | Liquid compositions containing urease inhibitors and glycol alkyl ethers |
US20140090432A1 (en) | 2012-10-01 | 2014-04-03 | Gary David McKnight | Liquid Formulations of Urease Inhibitors for Fertilizers |
WO2014100561A1 (en) | 2012-12-20 | 2014-06-26 | Rhodia Operations | Liquid dicyandiamide and/or alkyl thiophosphoric triamide compositions and their use in agricultural applications |
US8888886B1 (en) * | 2013-08-06 | 2014-11-18 | Garnett B Whitehurst | NBPT solutions for preparing urease inhibited urea fertilizers prepared from N-substituted morpholines |
WO2016054012A1 (en) | 2014-09-30 | 2016-04-07 | Iannotta Leahann | Solvent for thiophosphoric triamide or dicyandiamide solutions, and related methods |
WO2017031186A1 (en) | 2015-08-17 | 2017-02-23 | Rhodia Operations | High temperature amine-stabilized dcd and/or alkyl thiophosphoric triamide solvent systems and use in agricultural applications |
WO2017083714A1 (en) | 2015-11-11 | 2017-05-18 | Koch Agronomic Services, Llc | Composition containing n-(n-butyl) thiophosphoric triamide adducts and reaction products |
WO2017081183A1 (en) | 2015-11-12 | 2017-05-18 | Yara International Asa | Improved urea-based blend composition and method for the manufacture thereof |
EP3210959A1 (en) * | 2016-02-24 | 2017-08-30 | YARA International ASA | Liquid urease inhibitor formulation, method of manufacturing and solid particulates comprising it |
US20180002246A1 (en) | 2016-06-29 | 2018-01-04 | Rhodia Operations | Stabilized dcd and/or alkyl thiophosphoric triamide solvent systems and use in agricultural applications |
Non-Patent Citations (4)
Title |
---|
BOCK, B. R.; D. E. KISSEL: "Bulletin Y-206", 1988, NATIONAL FERTILIZER DEVELOPMENT CENTER, article "Ammonia Volatilization from Urea Fertilizers" |
GAUTNEY ET AL., IND. ENG. CHEM. PROD. RES. DEV., vol. 24, 1985, pages 155 - 181 |
GOOS, R.J., PROCEEDINGS OF THE 17TH N. CENTRAL EXTENSION INDUSTRY SOIL FERTILITY WORKSHOP, 1987 |
SULLIVAN, D.M.; HAVLIN, J. L., SOIL SCI. SOC. AM. J., vol. 56, 1992, pages 957 - 960 |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3113811A1 (en) | 2020-09-08 | 2022-03-11 | VALORISATION DES INNOVATIONS EN AGROFOURNITURES VEGETALES par abréviation VIA VEGETALE | Nitrogen fertilizer composition intended for root application |
CN114057522A (en) * | 2021-11-17 | 2022-02-18 | 中化农业(临沂)研发中心有限公司 | Biological stimulator composition containing double-effect slow-release nitrogen and preparation method thereof |
CN114057522B (en) * | 2021-11-17 | 2023-02-24 | 中化农业(临沂)研发中心有限公司 | Biological stimulin type liquid fertilizer containing double-effect slow-release nitrogen and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
AR114791A1 (en) | 2020-10-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US11148982B2 (en) | Reaction products and methods for making and using the same | |
US12134587B2 (en) | Reaction products and methods for making and using the same | |
CN106365927B (en) | Composition containing N- (normal-butyl) thiophosphoryl triamide adduct and reaction product | |
CA2931450C (en) | Nitrification inhibitors designed for urea and manure based fertilizers | |
EP1979294B1 (en) | Additive containing n-(n-butyl) thiophosphoric triamide for urea-based fertilizer | |
TWI421228B (en) | Fertilizer-polymer mixtures which inhibit nitrification in soils | |
AU2013202217B2 (en) | Urease inhibitor formulations | |
JP5455938B2 (en) | Double salt fertilizer increases crop yield | |
AU2011245115A1 (en) | Reaction products and methods for making and using the same | |
CA2947740C (en) | Increased longevity of the nitrogen content of soil through improved liquid delivery formulations of nitrification inhibitors designed for urea and manure based fertilizers | |
CN108473383B (en) | Composition containing N-n-butylthiophosphoric triamide adduct and reaction product | |
EP3575278A1 (en) | Liquid nitrogen fertilizer compositions and additives therefor | |
US11866384B2 (en) | Compositions and their use in agricultural applications | |
US20200102255A1 (en) | New method for fertilizing agricultural soil | |
WO2019204163A1 (en) | Liquid nitrogen fertilizer compositions and additives therefore | |
EP4359368A1 (en) | Combination of a pyrazole and a thiophosphoric triamide | |
CA2941176A1 (en) | An agricultural composition and methods for making and using the same | |
ZA200309364B (en) | Plant treatment composition. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 19720297 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 19720297 Country of ref document: EP Kind code of ref document: A1 |