JPH10324587A - Granular fertilizer coating agent - Google Patents
Granular fertilizer coating agentInfo
- Publication number
- JPH10324587A JPH10324587A JP9152817A JP15281797A JPH10324587A JP H10324587 A JPH10324587 A JP H10324587A JP 9152817 A JP9152817 A JP 9152817A JP 15281797 A JP15281797 A JP 15281797A JP H10324587 A JPH10324587 A JP H10324587A
- Authority
- JP
- Japan
- Prior art keywords
- component
- fertilizer
- weight
- coating
- polyol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003337 fertilizer Substances 0.000 title claims abstract description 63
- 239000011248 coating agent Substances 0.000 title claims abstract description 42
- 229920005862 polyol Polymers 0.000 claims abstract description 32
- 150000003077 polyols Chemical class 0.000 claims abstract description 30
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 24
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 24
- 238000000576 coating method Methods 0.000 claims abstract description 23
- 125000005702 oxyalkylene group Chemical group 0.000 claims abstract description 14
- 125000004185 ester group Chemical group 0.000 claims abstract description 12
- 229920005749 polyurethane resin Polymers 0.000 claims abstract description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 10
- -1 amine polyol Chemical class 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 5
- 238000010828 elution Methods 0.000 abstract description 15
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 abstract description 7
- 239000000178 monomer Substances 0.000 abstract description 5
- 125000002947 alkylene group Chemical group 0.000 abstract description 4
- 125000005442 diisocyanate group Chemical group 0.000 abstract description 4
- 229920000728 polyester Polymers 0.000 abstract description 3
- 150000001298 alcohols Chemical class 0.000 abstract description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 abstract description 2
- 239000008158 vegetable oil Substances 0.000 abstract description 2
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 description 15
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 9
- 239000004359 castor oil Substances 0.000 description 8
- 235000019438 castor oil Nutrition 0.000 description 8
- 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 8
- 230000000052 comparative effect Effects 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 5
- 230000000903 blocking effect Effects 0.000 description 5
- 239000012948 isocyanate Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 4
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 4
- 235000011130 ammonium sulphate Nutrition 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 239000004166 Lanolin Substances 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000001023 inorganic pigment Substances 0.000 description 2
- 229940039717 lanolin Drugs 0.000 description 2
- 235000019388 lanolin Nutrition 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000013268 sustained release Methods 0.000 description 2
- 239000012730 sustained-release form Substances 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- GFNDFCFPJQPVQL-UHFFFAOYSA-N 1,12-diisocyanatododecane Chemical compound O=C=NCCCCCCCCCCCCN=C=O GFNDFCFPJQPVQL-UHFFFAOYSA-N 0.000 description 1
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical compound O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 description 1
- QFGCFKJIPBRJGM-UHFFFAOYSA-N 12-[(2-methylpropan-2-yl)oxy]-12-oxododecanoic acid Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCC(O)=O QFGCFKJIPBRJGM-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- 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 1
- SNZYOYGFWBZAQY-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;2-methyloxirane Chemical compound CC1CO1.CCC(CO)(CO)CO SNZYOYGFWBZAQY-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- OUCNSFUASBNULY-UHFFFAOYSA-O [NH4+].[K].[O-][N+]([O-])=O Chemical compound [NH4+].[K].[O-][N+]([O-])=O OUCNSFUASBNULY-UHFFFAOYSA-O 0.000 description 1
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N tolylenediamine group Chemical group CC1=C(C=C(C=C1)N)N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
- C05G5/00—Fertilisers characterised by their form
- C05G5/30—Layered or coated, e.g. dust-preventing coatings
- C05G5/37—Layered or coated, e.g. dust-preventing coatings layered or coated with a polymer
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Fertilizers (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は粒状肥料用被覆剤に
関する。更に詳しくは、肥料成分溶出の遅延性が良好で
あり、かつブロッキング性のなく肥料への密着性に優
れ、また、被膜を溶剤を使用することなく、短時間で形
成することのできる被覆剤に関する。The present invention relates to a coating for granular fertilizer. More specifically, the present invention relates to a coating agent which has a good delay in elution of fertilizer components, has excellent blocking adhesion, and excellent adhesion to fertilizers, and can form a film in a short time without using a solvent. .
【0002】[0002]
【従来の技術】従来、粒状肥料の成分の効果を持続させ
るため、各種の合成高分子材料を粒状肥料の表面に被覆
した被覆肥料が検討されてきた。このような被覆材料の
うち、ウレタン系のものとしては、例えばポリイソシ
アネート、フェノールホルマリン縮合物、ヒドロキシ基
含有軟化剤、触媒アミンからなる無溶剤型被覆剤(特開
昭62−14474号公報);ポリイソシアネート
と、ウールまたはラノリン等から誘導されるポリオール
とを有機溶剤に溶解してなる被覆剤(特開平4−305
085号公報)等が提案されている。2. Description of the Related Art In order to maintain the effects of the components of granular fertilizers, coated fertilizers in which various synthetic polymer materials are coated on the surface of granular fertilizers have been studied. Among such coating materials, urethane-based coating materials include, for example, a solventless coating agent comprising a polyisocyanate, a phenol-formalin condensate, a hydroxy group-containing softener, and a catalytic amine (Japanese Patent Application Laid-Open No. Sho 62-14474); Coating agent obtained by dissolving polyisocyanate and polyol derived from wool or lanolin in an organic solvent (Japanese Patent Laid-Open No. 4-305
No. 085) has been proposed.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、上記
は肥料成分のブロッキングする問題があり、また肥料成
分溶出の遅延性にも問題がある。は所定の被膜厚とす
るためには何回も塗布乾燥を繰り返す必要があり、手間
がかかる問題がある。However, the above method has a problem of blocking the fertilizer component, and also has a problem of a delay in elution of the fertilizer component. It is necessary to repeat coating and drying many times in order to obtain a predetermined coating thickness, which is troublesome.
【0004】[0004]
【課題を解決するための手段】本発明者らは、上記問題
点を解決するため、遅延性が良好で、ブロッキング性の
ない被膜を形成できる無溶剤型被覆剤を得るべく鋭意検
討した結果、本発明に到達した。すなわち本発明は、ポ
リオール成分(A)とポリイソシアネート成分(B)か
ら誘導され、かつ分子内に、0.5〜20重量%の炭素
数3〜12のオキシアルキレン基と、1〜10重量%の
エステル基(−COO−)を含有するポリウレタン樹脂
からなることを特徴とする粒状肥料用被覆剤;ポリオー
ル成分(A)とポリイソシアネート成分(B)からな
り、該ポリオール成分(A)および/または該ポリイソ
シアネート成分(B)が分子内に炭素数3〜12のオキ
シアルキレン基とエステル基(−COO−)を含有し、
(A)と(B)の合計重量に基づいてオキシアルキレン
単位の含有量が0.5〜20重量%であり、(A)と
(B)の合計重量に基づいてエステル基含有量が1〜1
0重量%である、2成分系のポリウレタン形成性組成物
であることを特徴とする粒状肥料用被覆剤;さらに該被
覆剤で被覆されてなる粒状肥料である。Means for Solving the Problems In order to solve the above-mentioned problems, the present inventors have conducted intensive studies to obtain a solvent-free type coating agent which can form a film having good retardation and no blocking property. The present invention has been reached. That is, the present invention relates to a polyol component (A) and a polyisocyanate component (B), wherein 0.5 to 20% by weight of an oxyalkylene group having 3 to 12 carbon atoms and 1 to 10% by weight in a molecule. A granular fertilizer coating agent comprising a polyurethane resin containing an ester group (—COO—) of the following: a polyol component (A) and a polyisocyanate component (B), wherein the polyol component (A) and / or The polyisocyanate component (B) contains an oxyalkylene group having 3 to 12 carbon atoms and an ester group (—COO—) in the molecule,
The content of oxyalkylene units is 0.5 to 20% by weight based on the total weight of (A) and (B), and the ester group content is 1 to 20 based on the total weight of (A) and (B). 1
A coating material for a granular fertilizer, which is a two-component polyurethane-forming composition in an amount of 0% by weight; and a granular fertilizer further coated with the coating material.
【0005】[0005]
【発明の実施の形態】本発明におけるポリウレタン樹脂
は、分子内にオキシアルキレン基とエステル基(−CO
O−)を含有する。オキシアルキレン基としては、肥料
成分溶出の遅延性の点および肥料への密着性の点から、
通常炭素数3〜12のオキシアルキレン基、好ましくは
3〜6のオキシアルキレン基である。炭素数2以下では
過剰に肥料成分が溶出される場合があり、炭素数13以
上では肥料への密着性が低下する場合があり好ましくな
い。DETAILED DESCRIPTION OF THE INVENTION The polyurethane resin of the present invention has an oxyalkylene group and an ester group (-CO
O-). As an oxyalkylene group, from the point of delay of elution of fertilizer components and adhesion to fertilizer,
Usually, it is an oxyalkylene group having 3 to 12 carbon atoms, preferably an oxyalkylene group having 3 to 6 carbon atoms. If the number of carbon atoms is 2 or less, the fertilizer component may be excessively eluted, and if the number of carbon atoms is 13 or more, the adhesion to the fertilizer may decrease, which is not preferable.
【0006】該ポリウレタン樹脂中のオキシアルキレン
単位の含有量は、肥料成分溶出の遅延性の点および肥料
への密着性の点からから、通常0.5〜20重量%、好
ましくは1〜17重量%である。0.5重量%未満では
過剰に肥料成分が溶出される場合があり、20重量%を
超えると肥料への密着性が低下する場合があり好ましく
ない。[0006] The content of oxyalkylene units in the polyurethane resin is usually 0.5 to 20% by weight, preferably 1 to 17% by weight, from the viewpoint of delay in elution of fertilizer components and adhesion to fertilizers. %. If it is less than 0.5% by weight, the fertilizer component may be excessively eluted, and if it exceeds 20% by weight, the adhesion to the fertilizer may be reduced, which is not preferable.
【0007】また該ポリウレタン樹脂中のエステル基の
含有量は、肥料成分溶出後の残存被膜成分の加水分解性
の点から、通常1〜10重量%、好ましくは1.5〜8
重量%である。1重量%未満では被膜の肥料成分溶出後
の加水分解性が悪くなり、10重量%を超えると肥料成
分の溶出途中で被膜の加水分解が起こり徐放性が損なわ
れる。The content of the ester group in the polyurethane resin is usually 1 to 10% by weight, preferably 1.5 to 8%, in view of the hydrolyzability of the remaining film component after elution of the fertilizer component.
% By weight. If it is less than 1% by weight, the hydrolyzability of the film after elution of the fertilizer component is poor, and if it exceeds 10% by weight, the film is hydrolyzed during the elution of the fertilizer component and the sustained release property is impaired.
【0008】該ポリウレタン樹脂中への炭素数3〜12
のオキシアルキレン基、エステル基の導入方法は特に限
定はなく、ポリオール成分(A)由来、ポリイソシアネ
ート成分(B)由来のいずれでもかまわない。さらに、
2種の基が単独成分の由来でも異なる成分由来でもよ
い。[0008] 3 to 12 carbon atoms in the polyurethane resin
The method for introducing the oxyalkylene group and ester group is not particularly limited, and may be derived from the polyol component (A) or the polyisocyanate component (B). further,
The two groups may be from a single component or from different components.
【0009】本発明における粒状肥料用被覆剤は、ポリ
オール成分(A)とポリイソシアネート成分(B)から
誘導されるポリウレタン樹脂であり、また、ポリオール
成分(A)とポリイソシアネート成分(B)からなる2
成分系のポリウレタン樹脂である。オキシアルキレン単
位の含有量は、肥料成分溶出の遅延性の点および肥料へ
の密着性の点からから、(A)と(B)の合計重量に対
し、通常0.5〜20重量%、好ましくは1〜17重量
%である。また、エステル基含有量は、肥料成分溶出の
遅延性の点および肥料への密着性の点からから、(A)
と(B)の合計重量に基づき、通常1〜10重量%、好
ましくは1.5〜8重量%である。1重量%未満では被
膜の肥料成分溶出後の加水分解性が悪くなり、10重量
%を超えると肥料成分の溶出途中で被膜の加水分解が起
こり徐放性が損なわれる。The coating material for granular fertilizer in the present invention is a polyurethane resin derived from a polyol component (A) and a polyisocyanate component (B), and comprises a polyol component (A) and a polyisocyanate component (B). 2
It is a component-based polyurethane resin. The content of the oxyalkylene unit is usually 0.5 to 20% by weight, preferably 0.5 to 20% by weight, based on the total weight of (A) and (B), from the viewpoint of delay in elution of the fertilizer component and adhesion to the fertilizer. Is 1 to 17% by weight. Further, the ester group content is determined from the viewpoint of the delay of elution of the fertilizer component and the adhesion to the fertilizer, (A)
It is usually 1 to 10% by weight, preferably 1.5 to 8% by weight, based on the total weight of (B) and (B). If it is less than 1% by weight, the hydrolyzability of the film after elution of the fertilizer component is poor, and if it exceeds 10% by weight, the film is hydrolyzed during the elution of the fertilizer component and the sustained release property is impaired.
【0010】ポリオール成分(A)としては、たとえば
植物油およびその誘導体(たとえばヒマシ油、ヒマシ
油のアルキレンオキサイド付加体、ヒマシ油脂肪酸の多
価アルコール変性体等)、低分子多官能アルコールの
アルキレンオキサイド付加体(たとえばグリセリン、ト
リメチロールプロパンのプロピレンオキサイド、ブチレ
ンオキサイド、スチレンオキサイドの単独付加体、共付
加体等)、低分子多官能カルボン酸のアルキレンオキ
サイド付加体(たとえばドデカン二酸のプロピレンオキ
サイド、ブチレンオキサイド、スチレンオキサイドの単
独付加体、共付加体等)低分子多官能ポリエステルの
アルキレンオキサイド付加体(たとえばグリセリンとド
デカン二酸とのポリエステルのプロピレンオキサイド、
ブチレンオキサイド、スチレンオキサイドの単独付加
体、共付加体等);およびこれら2種以上の混合物が挙
げられる。ポリオール1分子中の官能基(水酸基)数は
皮膜形成性の点から通常2〜10であり、好ましくは2
〜6である。Examples of the polyol component (A) include vegetable oils and derivatives thereof (eg, castor oil, alkylene oxide adducts of castor oil, modified polyhydric alcohols of castor oil fatty acids, etc.) and alkylene oxide additions of low molecular weight polyfunctional alcohols. (Eg, glycerin, trimethylolpropane propylene oxide, butylene oxide, homo-adducts and co-adducts of styrene oxide), low-molecular weight polyfunctional carboxylic acid alkylene oxide adducts (eg, dodecane diacid propylene oxide, butylene oxide) Styrene oxide homo-adducts, co-adducts, etc.) alkylene oxide adducts of low molecular weight polyfunctional polyesters (for example, propylene oxide of polyester of glycerin and dodecanedioic acid,
Butylene oxide, a single adduct of styrene oxide, a co-adduct and the like); and a mixture of two or more of these. The number of functional groups (hydroxyl groups) in one molecule of the polyol is usually 2 to 10 in view of film forming property, and preferably 2 to 10.
~ 6.
【0011】また、被膜形成性の低温での硬化性を付与
する目的で、必要によりアミン系ポリオール(A−1)
をポリオール成分の一部として併用してもよい。アミン
系ポリオール(A−1)としては、例えば炭素数3〜
20のオキシアルキレン化ポリアミン(エチレンジアミ
ンのプロピレンオキサイド4モル付加体、ジエチレント
リアミンのプロピレンオキサイド5モル付加体、トリエ
チレンテトラミンのプロピレンオキサイド6モル付加
体、トリレンジアミンのエチレンオキサイド4モル付加
体等);アルカノールアミン(トリプロパノールアミ
ン、トリプロパノールアミンのプロピレンオキサイド3
モル付加体等)が挙げられる。これらのうち、被膜の硬
化速度および硬化被膜の耐ブロッキング性の点から好ま
しいものは上記であり、分子内に少なくとも3個の水
酸基を含有する上記がさらに好ましい。アミン系ポリ
オール(A−1)に基づく3級窒素含有量は、室温での
硬化性を付与するためには、(A)と(B)の合計重量
に対し、通常0.01〜1.5重量%、好ましくは0.
1〜1.0重量%である。0.01重量%未満では室温
での硬化速度が遅くなり、1.5重量%を超えると硬化
速度が速くなりすぎ、均質な被膜形成が困難となること
がある。In order to impart film-forming curability at a low temperature, an amine-based polyol (A-1) is optionally used.
May be used in combination as a part of the polyol component. Examples of the amine-based polyol (A-1) include, for example, C3 to C3.
20 oxyalkylenated polyamines (such as a 4-mol adduct of propylene oxide with ethylenediamine, a 5-mol adduct of propylene oxide with diethylenetriamine, a 6-mol adduct of propylene oxide with triethylenetetramine, and a 4-mol adduct of tolylenediamine with ethylene oxide); Amines (tripropanolamine, propylene oxide 3 of tripropanolamine)
Mole adduct). Among them, those preferred from the viewpoint of the curing speed of the coating and the blocking resistance of the cured coating are described above, and those containing at least three hydroxyl groups in the molecule are more preferred. The tertiary nitrogen content based on the amine polyol (A-1) is usually 0.01 to 1.5 with respect to the total weight of (A) and (B) in order to impart curability at room temperature. % By weight, preferably 0.
1 to 1.0% by weight. If it is less than 0.01% by weight, the curing rate at room temperature will be slow, and if it exceeds 1.5% by weight, the curing rate will be too fast, and it may be difficult to form a uniform film.
【0012】さらに、前記のポリオールを少量のポリイ
ソシアネートと予め反応させたポリウレタンポリオール
プレポリマーをポリオール成分(A)として用いてもか
まわない。ポリオールの水酸基と、ポリイソシアネート
のイソシアネート基の当量比(OH/NCO)は、通常
(1.2〜100)/1、好ましくは(2〜50)/1
である。Further, a polyurethane polyol prepolymer obtained by previously reacting the above polyol with a small amount of polyisocyanate may be used as the polyol component (A). The equivalent ratio (OH / NCO) of the hydroxyl group of the polyol to the isocyanate group of the polyisocyanate is usually (1.2 to 100) / 1, preferably (2 to 50) / 1.
It is.
【0013】ポリオール成分(A)中には、必要により
他の成分として公知のポリマー、溶剤等を添加してもか
まわない。The polyol component (A) may contain other known components such as a polymer and a solvent, if necessary.
【0014】ポリイソシアネ−ト成分(B)としては、
例えばジイソシアネートモノマー〔芳香族イソシアネ
ート(トリレンジイソシアネート、ジフェニルメタンジ
イソシアネートなど)、芳香脂肪族イソシアネート(キ
シリレンジイソシアネート、α、α、α'、α'−テトラ
メチルキシリレンジイソシアネートなど)、脂環式イソ
シアネート(イソホロンジイソシネート、ジシクロヘキ
シルメタンジイソシアネートなど)、脂肪族イソシアネ
ート(ヘキサメチレンジイソシアネート、ドデカメチレ
ンジイソシアネートなど)〕;これらジイソシアネー
トモノマーの変性体(イソシアヌレート体、ビューレッ
ト体、ウレトジオン体、トリメチロールプロパン付加体
など);ポリイソシアネートプレポリマー(たとえば
ポリオールと過剰のイソシアネート化合物との反応
物);およびこれらの2種以上の混合物が挙げられる。
これらのうち好ましいものは反応性の高い芳香族ジイソ
シアネートモノマー、その変性体およびプレポリマーで
あり、特に好ましいものはジフェニルメタンジイソシア
ネートモノマーおよびそのプレポリマーである。ポリイ
ソシアネート1分子中の官能基(イソシアネート基)数
は皮膜形成性の点から通常2〜10であり、好ましくは
2〜6である。As the polyisocyanate component (B),
For example, diisocyanate monomers [aromatic isocyanates (tolylene diisocyanate, diphenylmethane diisocyanate, etc.), araliphatic isocyanates (xylylene diisocyanate, α, α, α ', α'-tetramethylxylylene diisocyanate, etc.), alicyclic isocyanates (isophorone Diisocyanate, dicyclohexylmethane diisocyanate, etc.), aliphatic isocyanates (hexamethylene diisocyanate, dodecamethylene diisocyanate, etc.)]; modified products of these diisocyanate monomers (isocyanurate, buret, uretdione, trimethylolpropane adduct, etc.) A polyisocyanate prepolymer (eg, a reactant of a polyol with an excess of an isocyanate compound); and two or more of these. Mixtures are mentioned.
Of these, preferred are highly reactive aromatic diisocyanate monomers, modified products and prepolymers, and particularly preferred are diphenylmethane diisocyanate monomers and prepolymers thereof. The number of functional groups (isocyanate groups) in one molecule of the polyisocyanate is usually 2 to 10, preferably 2 to 6, from the viewpoint of film-forming properties.
【0015】さらに、前記のポリイソシアネートを少量
のポリオールと予め反応させたポリウレタンポリイソシ
アネートをポリイソシアネート成分(B)として用いて
もかまわない。ポリイソシアネートのイソシアネート基
とポリオールの水酸基の当量比(NCO/OH)は、通
常(1.2〜100)/1、好ましくは(2〜50)/
1である。Further, a polyurethane polyisocyanate obtained by previously reacting the above-mentioned polyisocyanate with a small amount of a polyol may be used as the polyisocyanate component (B). The equivalent ratio (NCO / OH) of the isocyanate group of the polyisocyanate to the hydroxyl group of the polyol is usually (1.2 to 100) / 1, preferably (2 to 50) /
It is one.
【0016】ポリイソシアネート成分(B)には、必要
により他の成分として公知のポリマー、溶剤等を添加し
てもかまわない。The polyisocyanate component (B) may contain other known components such as a polymer and a solvent, if necessary.
【0017】成分(A)の水酸基と、成分(B)のイソ
シアネート基の当量比(OH/NCO)は、通常(85
〜115)/(115〜85)、好ましくは(90〜1
10)/(110〜90)である。比率が上記範囲外で
は十分な被膜強度および耐久性が得られないことがあ
る。The equivalent ratio (OH / NCO) of the hydroxyl group of the component (A) to the isocyanate group of the component (B) is usually (85 / NCO).
To 115) / (115 to 85), preferably (90 to 1)
10) / (110-90). If the ratio is out of the above range, sufficient coating strength and durability may not be obtained.
【0018】本発明において(A)、(B)の混合方法
および被覆剤としての使用方法については特に限定され
ず、(A)と(B)を予め混合し被覆剤として用いる
方法、(A)と(B)から誘導されるウレタン樹脂の
溶剤(たとえばトルエン、キシレン、クロロホルム、テ
トラヒドロフラン、ジメチルホルムアミド)希釈品を被
覆剤として用いる方法等が挙げられる。粘度によって異
なるが、通常、樹脂濃度は5〜100%である。好まし
くは希釈剤を用いる必要がなく、乾燥行程が省けるとい
う利点を持つである。In the present invention, the method of mixing (A) and (B) and the method of using it as a coating agent are not particularly limited, and a method in which (A) and (B) are mixed in advance and used as a coating agent, And a method in which a solvent (for example, toluene, xylene, chloroform, tetrahydrofuran, or dimethylformamide) diluted with a urethane resin derived from (B) is used as the coating agent. Although it depends on the viscosity, the resin concentration is usually 5 to 100%. Preferably, there is no need to use a diluent, and there is an advantage that the drying step can be omitted.
【0019】本発明の被覆剤には、必要により他の成分
として公知のポリマー、分散剤、界面活性剤、無機顔料
等を添加してもよい。上記ポリマーの具体例としてはポ
リエステル樹脂、ポリアミド樹脂、エポキシ樹脂、塩化
ビニル−酢酸ビニル共重合樹脂などをあげることができ
る。また、無機顔料の例としては、カオリン、タルク、
炭酸カルシウム、マイカ、クレー、硅酸カルシウムなど
があげられる。If necessary, the coating agent of the present invention may contain other known components such as a polymer, a dispersant, a surfactant and an inorganic pigment. Specific examples of the above polymer include polyester resin, polyamide resin, epoxy resin, vinyl chloride-vinyl acetate copolymer resin, and the like. Examples of inorganic pigments include kaolin, talc,
Examples include calcium carbonate, mica, clay, and calcium silicate.
【0020】本発明の被覆剤を使用できる肥料は粒状で
あれば特に限定はなく、例えば、尿素、硫安、硝安、塩
化カリの如き単肥や、硫化燐安、燐化安、燐硝安カリの
如き複合肥料が代表例として挙げられる。The fertilizer to which the coating agent of the present invention can be used is not particularly limited as long as it is granular. For example, monofertilizers such as urea, ammonium sulfate, ammonium nitrate, potassium chloride, and phosphorus ammonium sulfide, ammonium phosphide, and potassium nitrate ammonium can be used. Compound fertilizers such as those described above are typical examples.
【0021】本発明の被覆剤を使用する場合の粒状肥料
への被覆方法としては、流動浮遊状態にある粒状肥料
に対しスプレー粉霧する方法、回転パン中にある粒状
肥料に対しスプレー粉霧する方法が挙げられる。被覆剤
被膜は塗布後10〜20分で硬化するが、60〜100
℃の熱風で加熱すれば更に短時間で硬化させることがで
きる。As a method of coating the granular fertilizer when the coating agent of the present invention is used, a method of spraying and atomizing the granular fertilizer in a fluid floating state, and a method of spraying and atomizing the granular fertilizer in a rotating pan. Method. The coating film cures in 10 to 20 minutes after application, but 60 to 100
If it is heated with hot air at ℃, it can be cured in a shorter time.
【0022】このようにして得られた被覆粒状肥料は被
覆途中でブロッキング現象を引き起こすこともなく、ま
た保管中にブロッキングすることもない。また、該被覆
剤は短い時間で任意の厚さに被覆することができ、得ら
れた粒状肥料は水中に浸積した場合その肥料成分の溶出
量を適度に制御することができる。The coated granular fertilizer thus obtained does not cause a blocking phenomenon during coating and does not block during storage. Further, the coating agent can be coated to an arbitrary thickness in a short time, and when the obtained granular fertilizer is immersed in water, the elution amount of the fertilizer component can be appropriately controlled.
【0023】[0023]
【実施例】以下実施例により本発明を更に詳細に説明す
るが、本発明はこれに限定されるものではない。尚、以
下において「部」は重量部、「%」は重量%を示す。The present invention will be described in more detail with reference to the following Examples, but it should not be construed that the invention is limited thereto. In the following, "parts" indicates parts by weight and "%" indicates% by weight.
【0024】製造例、実施例および比較例における使用
原料の略号の意味は下記のとおりである。 〔ポリオール(A)成分〕 A1:ヒマシ油(分子量1000、水酸基価161) A2:ヒマシ油プロピレンオキサイド付加体(分子量1
350、水酸基価125) A3:ヒマシ油(分子量1000、水酸基価161)7
00部とペンタエリスリトールのプロピレンオキサイド
付加体(分子量400)300部の混合物(水酸基価2
80) 〔ポリイソシアネート(B)成分〕 B1:グリセリンのプロピレンオキサイド付加体(分子
量3000)とジフェニルメタンジイソシアネートの反
応物(NCO%15.1) B2:トリメチロールプロパンのプロピレンオキサイド
付加体(分子量700)とジフェニルメタンジイソシア
ネートの反応物(NCO%18.9) B3:ヒマシ油とジフェニルメタンジイソシアネートの
反応物(NCO%19.1) 〔アミン系ポリオール(A−1)成分〕 C1:エチレンジアミンのプロピレンオキサイド付加体
(分子量300) C2:エチレンジアミンのプロピレンオキサイド付加体
(分子量400)The meanings of the abbreviations of the raw materials used in Production Examples, Examples and Comparative Examples are as follows. [Polyol (A) component] A1: Castor oil (molecular weight: 1,000, hydroxyl value: 161) A2: Castor oil propylene oxide adduct (molecular weight: 1)
A3: castor oil (molecular weight 1000, hydroxyl value 161) 7
00 parts and 300 parts of a propylene oxide adduct of pentaerythritol (molecular weight 400) (hydroxyl value 2
80) [Polyisocyanate (B) component] B1: Reaction product of propylene oxide adduct of glycerin (molecular weight 3000) and diphenylmethane diisocyanate (NCO% 15.1) B2: Propylene oxide adduct of trimethylolpropane (molecular weight 700) Reaction product of diphenylmethane diisocyanate (NCO% 18.9) B3: Reaction product of castor oil and diphenylmethane diisocyanate (NCO% 19.1) [Amine-based polyol (A-1) component] C1: Propylene oxide adduct of ethylenediamine (molecular weight) 300) C2: Propylene oxide adduct of ethylenediamine (molecular weight 400)
【0025】実施例1〜5 表1に示す配合量のポリオール成分(A)、ポリイソシ
アネート成分(B)およびアミン系ポリオール(A−
1)を使用し被覆剤を作成した。粒状肥料への被覆は、
噴流層による流動コーテイング装置を用い、装置内で浮
遊している平均粒子径が3〜5mmである市販の硫安粒
状肥料1kgに、各被覆剤を固形分として60gスプレ
ー粉霧で添加し被覆を行い、室温硬化させて被覆剤被覆
率6重量%の本発明の被覆粒状肥料を得た。Examples 1 to 5 Polyol component (A), polyisocyanate component (B) and amine-based polyol (A-
A coating agent was prepared using 1). The coating on granular fertilizer is
Using a fluid coating apparatus with a spouted bed, 60 g of each coating agent is added as a solid content to 1 kg of a commercially available ammonium sulfate fertilizer having an average particle diameter of 3 to 5 mm, which is suspended in the apparatus, by spraying and atomizing, and coating is performed. After curing at room temperature, a coated granular fertilizer of the present invention having a coating agent coverage of 6% by weight was obtained.
【0026】[0026]
【表1】 [Table 1]
【0027】比較例1 特開平4−305085号公報明細書の実施例3の記載
の方法に従って、ラノリンアルコール10部、2,4−
トリレンジイソシアネート10部およびテトラクロロエ
チレン50部を混合溶解した溶液に、実施例1で用いた
粒状肥料を浸漬し、100℃で20分乾燥する操作を繰
り返して、被覆率10重量%の比較の被覆粒状肥料を得
た。Comparative Example 1 According to the method described in Example 3 of JP-A-4-305085, 10 parts of lanolin alcohol, 2,4-
The operation of immersing the granular fertilizer used in Example 1 in a solution obtained by mixing and dissolving 10 parts of tolylene diisocyanate and 50 parts of tetrachloroethylene and drying it at 100 ° C. for 20 minutes is repeated to obtain a coated granular material having a coverage of 10% by weight. Got fertilizer.
【0028】比較例2 特開昭62−144474号公報明細書の実施例1の記
載の方法に従って、1モルのフェノールと1.2モルの
ホルムアルデヒドから調整したベンジルエーテル樹脂、
ヒマシ油、およびジアセトンアルコール混合物50部と
ジフェニルメタンジイソシアネート50部を混合溶解し
た溶液を、ジメチルアミン含有窒素ガスを導入しなが
ら、実施例1と同様の操作を行い、被覆率10重量%の
比較の被覆粒状肥料を得た。Comparative Example 2 A benzyl ether resin prepared from 1 mol of phenol and 1.2 mol of formaldehyde according to the method described in Example 1 of JP-A-62-144474.
A solution prepared by mixing and dissolving 50 parts of castor oil and 50 parts of diacetone alcohol mixture with 50 parts of diphenylmethane diisocyanate was subjected to the same operation as in Example 1 while introducing dimethylamine-containing nitrogen gas. A coated granular fertilizer was obtained.
【0029】比較例3 ポリカプロラクトン樹脂(ダイセル化学工業製、「プラ
クセルH7000」)をメチルエチルケトンに溶解して
25%溶液を作成し、この溶液に実施例1で用いた粒状
肥料を浸漬し100℃で20分乾燥する操作を繰り返し
て、被覆率10重量%の比較の被覆粒状肥料を得た。Comparative Example 3 A 25% solution was prepared by dissolving a polycaprolactone resin ("Placcel H7000", manufactured by Daicel Chemical Industries, Ltd.) in methyl ethyl ketone, and the granular fertilizer used in Example 1 was immersed in this solution and heated at 100.degree. The operation of drying for 20 minutes was repeated to obtain a comparative coated granular fertilizer having a coverage of 10% by weight.
【0030】実施例1〜5、比較例1〜3で得られた被
覆粒状肥料を10gずつ、各々別々に200mlの水中
に入れて25℃で放置し、水相の導電率を測定し硫安の
溶出率を算出した。硫安の溶出率を表2に示す。10 g of each of the coated granular fertilizers obtained in Examples 1 to 5 and Comparative Examples 1 to 3 was separately placed in 200 ml of water and allowed to stand at 25 ° C., and the conductivity of the aqueous phase was measured. The elution rate was calculated. Table 2 shows the dissolution rate of ammonium sulfate.
【0031】[0031]
【表2】 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 被覆肥料中硫安の溶出率(%) 1ヶ月後 2ヶ月後 3ヶ月後 4ヶ月後 5ヶ月後 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 実施例1 0 13.0 30.2 56.7 82.3 2 0 25.3 55.9 80.3 97.5 3 0 33.2 69.1 85.3 99.2 4 0 12.7 29.3 52.9 80.3 5 0 24.9 52.7 77.9 95.9 6 0 30.0 62.9 87.4 96.7 7 0 29.3 59.3 86.2 94.7 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 比較例1 1.0 1.5 1.6 5.5 90.2 2 4.5 10.5 100 − − 3 100 − − − − −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− Table 2-Dissolution rate (%) of ammonium sulfate in coated fertilizer 1 After 2 months After 3 months After 4 months After 5 months 5 months -------------------------- Example 10 13.0 30.2 56.7 82.3 2 20 55.3 55.9 80.3 97.5 30 33.2 69.1 85.3 99.2 40 12.7 29. 3 52.9 80.3 50 24.9 52.7 77.9 95.9 60 30.0 62.9 87.4 96.7 70 29.3 59.3 86.2 94.7- −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− Comparative example 1 1.0 1.5 1.6 5.5 5.5 90 .2 2 4.5 10.5 100 − − 3 100 − − − − −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−
【0032】[0032]
【発明の効果】本発明の粒状肥料用被覆剤は、下記の効
果を奏する。 (1)溶剤を使用することなく、短時間で粒状肥料表面
に有機質被膜を形成することができる。 (2)従来より薄い膜厚でも均質な被膜を形成すること
ができる。 (3)肥料に長期にわたり遅延性を付与し、肥料成分の
土中への溶出量を制御することができる。 (4)肥料成分放出後の樹脂被膜は、土中の酸またはア
ルカリによって加水分解するので、最終的に土中に残存
することがない。The coating agent for granular fertilizer of the present invention has the following effects. (1) An organic film can be formed on the surface of the granular fertilizer in a short time without using a solvent. (2) A uniform film can be formed even with a film thickness smaller than the conventional one. (3) The fertilizer can be given a delay over a long period of time, and the amount of the fertilizer component eluted into the soil can be controlled. (4) Since the resin film after the release of the fertilizer component is hydrolyzed by the acid or alkali in the soil, it does not finally remain in the soil.
─────────────────────────────────────────────────────
────────────────────────────────────────────────── ───
【手続補正書】[Procedure amendment]
【提出日】平成10年3月18日[Submission date] March 18, 1998
【手続補正1】[Procedure amendment 1]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】特許請求の範囲[Correction target item name] Claims
【補正方法】変更[Correction method] Change
【補正内容】[Correction contents]
【特許請求の範囲】[Claims]
Claims (4)
ート成分(B)から誘導され、かつ分子内に、0.5〜
20重量%の炭素数3〜12のオキシアルキレン基と、
1〜10重量%のエステル基(−COO−)を含有する
ポリウレタン樹脂からなることを特徴とする粒状肥料用
被覆剤。1. A polymer derived from a polyol component (A) and a polyisocyanate component (B) and having a molecular weight of 0.5 to
20% by weight of an oxyalkylene group having 3 to 12 carbon atoms,
A coating material for granular fertilizer, comprising a polyurethane resin containing 1 to 10% by weight of an ester group (-COO-).
ート成分(B)からなり、該ポリオール成分(A)およ
び/または該ポリイソシアネート成分(B)が分子内に
炭素数3〜12のオキシアルキレン基とエステル基(−
COO−)を含有し、(A)と(B)の合計重量に基づ
いてオキシアルキレン単位の含有量が0.5〜20重量
%であり、(A)と(B)の合計重量に基づいてエステ
ル基含有量が1〜10重量%である、2成分系のポリウ
レタン形成性組成物であることを特徴とする粒状肥料用
被覆剤。2. A composition comprising a polyol component (A) and a polyisocyanate component (B), wherein the polyol component (A) and / or the polyisocyanate component (B) have an oxyalkylene group having 3 to 12 carbon atoms in a molecule. Ester group (-
COO-), the content of oxyalkylene units is 0.5 to 20% by weight based on the total weight of (A) and (B), and the content of (A) and (B) is based on the total weight of (A) and (B). A coating material for granular fertilizer, which is a two-component polyurethane-forming composition having an ester group content of 1 to 10% by weight.
価以上のアミン系ポリオール(A−1)を用いてなる請
求項2または3記載の粒状肥料用被覆剤。3. As part of the polyol component (A), 3
The coating material for granular fertilizer according to claim 2 or 3, comprising an amine polyol (A-1) having a valency or higher.
覆されてなる粒状肥料。4. A granular fertilizer coated with the coating agent according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15281797A JP3161997B2 (en) | 1997-05-26 | 1997-05-26 | Coating agent for granular fertilizer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15281797A JP3161997B2 (en) | 1997-05-26 | 1997-05-26 | Coating agent for granular fertilizer |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH10324587A true JPH10324587A (en) | 1998-12-08 |
JP3161997B2 JP3161997B2 (en) | 2001-04-25 |
Family
ID=15548815
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15281797A Expired - Lifetime JP3161997B2 (en) | 1997-05-26 | 1997-05-26 | Coating agent for granular fertilizer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3161997B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6364925B1 (en) * | 1999-12-10 | 2002-04-02 | Bayer Corporation | Polyurethane encapsulated fertilizer having improved slow-release properties |
JP2007277429A (en) * | 2006-04-07 | 2007-10-25 | Chisso Asahi Hiryo Kk | Polyols, polyurethane coatings and coated particulate plant actives |
JP2011178650A (en) * | 2010-02-08 | 2011-09-15 | Central Glass Co Ltd | Method for producing coated granular water-soluble substance |
WO2013077725A3 (en) * | 2011-11-21 | 2013-07-18 | Malaysian Palm Oil Board | A controlled-release fertilizer |
JP2014512938A (en) * | 2011-02-09 | 2014-05-29 | オーエムエス・インベストメンツ・インク | Method and system for coating granular substrates |
WO2017043413A1 (en) * | 2015-09-11 | 2017-03-16 | 住友化学株式会社 | Coated granular fertilizer, method for producing coated granular fertilizer, and fertilizer composition |
JP2017202970A (en) * | 2016-05-09 | 2017-11-16 | 三洋化成工業株式会社 | Polyurethane resin formative composition for fertilizer coating material |
-
1997
- 1997-05-26 JP JP15281797A patent/JP3161997B2/en not_active Expired - Lifetime
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6364925B1 (en) * | 1999-12-10 | 2002-04-02 | Bayer Corporation | Polyurethane encapsulated fertilizer having improved slow-release properties |
JP2007277429A (en) * | 2006-04-07 | 2007-10-25 | Chisso Asahi Hiryo Kk | Polyols, polyurethane coatings and coated particulate plant actives |
JP2011178650A (en) * | 2010-02-08 | 2011-09-15 | Central Glass Co Ltd | Method for producing coated granular water-soluble substance |
JP2014512938A (en) * | 2011-02-09 | 2014-05-29 | オーエムエス・インベストメンツ・インク | Method and system for coating granular substrates |
US11142488B2 (en) | 2011-02-09 | 2021-10-12 | Everris International B.V. | Methods and systems for coating granular substrates |
WO2013077725A3 (en) * | 2011-11-21 | 2013-07-18 | Malaysian Palm Oil Board | A controlled-release fertilizer |
US9090517B2 (en) | 2011-11-21 | 2015-07-28 | Malaysian Palm Oil Board | Controlled-release fertilizer |
WO2017043413A1 (en) * | 2015-09-11 | 2017-03-16 | 住友化学株式会社 | Coated granular fertilizer, method for producing coated granular fertilizer, and fertilizer composition |
CN108025992A (en) * | 2015-09-11 | 2018-05-11 | 住友化学株式会社 | Coated granular fertilizer, the manufacture method of coated granular fertilizer and Ru 2006101161 |
CN108025992B (en) * | 2015-09-11 | 2021-04-30 | 住友化学株式会社 | Coated granular fertilizer, method for producing coated granular fertilizer, and fertilizer composition |
US11001539B2 (en) | 2015-09-11 | 2021-05-11 | Sumitomo Chemical Company, Limited | Coated granular fertilizer, method for producing coated granular fertilizer, and fertilizer compostion |
JP2017202970A (en) * | 2016-05-09 | 2017-11-16 | 三洋化成工業株式会社 | Polyurethane resin formative composition for fertilizer coating material |
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