AU535697B2 - Improved aqueous soap-based lubricant composition - Google Patents
Improved aqueous soap-based lubricant compositionInfo
- Publication number
- AU535697B2 AU535697B2 AU61237/80A AU6123780A AU535697B2 AU 535697 B2 AU535697 B2 AU 535697B2 AU 61237/80 A AU61237/80 A AU 61237/80A AU 6123780 A AU6123780 A AU 6123780A AU 535697 B2 AU535697 B2 AU 535697B2
- Authority
- AU
- Australia
- Prior art keywords
- percent
- weight
- concentrate
- fatty acid
- water
- 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.)
- Ceased
Links
- 239000000203 mixture Substances 0.000 title claims description 37
- 239000000314 lubricant Substances 0.000 title claims description 21
- 239000000344 soap Substances 0.000 title claims description 18
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 35
- 239000000194 fatty acid Substances 0.000 claims description 35
- 229930195729 fatty acid Natural products 0.000 claims description 35
- 150000004665 fatty acids Chemical class 0.000 claims description 33
- 239000012141 concentrate Substances 0.000 claims description 25
- 239000004094 surface-active agent Substances 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 21
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 18
- YPIFGDQKSSMYHQ-UHFFFAOYSA-N 7,7-dimethyloctanoic acid Chemical compound CC(C)(C)CCCCCC(O)=O YPIFGDQKSSMYHQ-UHFFFAOYSA-N 0.000 claims description 15
- 239000002738 chelating agent Substances 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 9
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 8
- 150000002191 fatty alcohols Chemical class 0.000 claims description 8
- 239000003784 tall oil Substances 0.000 claims description 7
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 6
- 229960001484 edetic acid Drugs 0.000 claims description 6
- 230000001050 lubricating effect Effects 0.000 claims description 5
- KKEBXNMGHUCPEZ-UHFFFAOYSA-N 4-phenyl-1-(2-sulfanylethyl)imidazolidin-2-one Chemical compound N1C(=O)N(CCS)CC1C1=CC=CC=C1 KKEBXNMGHUCPEZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000000908 ammonium hydroxide Substances 0.000 claims description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 1
- -1 more particularly Substances 0.000 description 35
- 239000002253 acid Substances 0.000 description 15
- 125000005702 oxyalkylene group Chemical group 0.000 description 12
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000002585 base Substances 0.000 description 7
- 230000002209 hydrophobic effect Effects 0.000 description 7
- 125000004430 oxygen atom Chemical group O* 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000008399 tap water Substances 0.000 description 7
- 235000020679 tap water Nutrition 0.000 description 7
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 6
- 239000012895 dilution Substances 0.000 description 6
- 238000010790 dilution Methods 0.000 description 6
- 235000019602 lubricity Nutrition 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 5
- 244000060011 Cocos nucifera Species 0.000 description 4
- 235000013162 Cocos nucifera Nutrition 0.000 description 4
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 3
- ZFIVKAOQEXOYFY-UHFFFAOYSA-N Diepoxybutane Chemical compound C1OC1C1OC1 ZFIVKAOQEXOYFY-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 239000004519 grease Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 235000021313 oleic acid Nutrition 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 150000003333 secondary alcohols Chemical class 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 125000006353 oxyethylene group Chemical group 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- HNSDLXPSAYFUHK-UHFFFAOYSA-N 1,4-bis(2-ethylhexyl) sulfosuccinate Chemical compound CCCCC(CC)COC(=O)CC(S(O)(=O)=O)C(=O)OCC(CC)CCCC HNSDLXPSAYFUHK-UHFFFAOYSA-N 0.000 description 1
- QGJDXUIYIUGQGO-UHFFFAOYSA-N 1-[2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]pyrrolidine-2-carboxylic acid Chemical compound CC(C)(C)OC(=O)NC(C)C(=O)N1CCCC1C(O)=O QGJDXUIYIUGQGO-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- JKTAIYGNOFSMCE-UHFFFAOYSA-N 2,3-di(nonyl)phenol Chemical compound CCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCC JKTAIYGNOFSMCE-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- URDCARMUOSMFFI-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound OCCN(CC(O)=O)CCN(CC(O)=O)CC(O)=O URDCARMUOSMFFI-UHFFFAOYSA-N 0.000 description 1
- CDOUZKKFHVEKRI-UHFFFAOYSA-N 3-bromo-n-[(prop-2-enoylamino)methyl]propanamide Chemical compound BrCCC(=O)NCNC(=O)C=C CDOUZKKFHVEKRI-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 101100080971 Caenorhabditis elegans cps-6 gene Proteins 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical class C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 150000002193 fatty amides Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229940102253 isopropanolamine Drugs 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 238000005555 metalworking Methods 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Substances [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- UXIDHQPACNSJJP-UHFFFAOYSA-M sodium;2-[2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetate Chemical compound [Na+].OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC([O-])=O UXIDHQPACNSJJP-UHFFFAOYSA-M 0.000 description 1
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
- 235000014214 soft drink Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 230000010148 water-pollination Effects 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Lubricants (AREA)
Description
PROVED AQUEOUS SOAP-BASED LUBRICANT COMPOSITION
1. Field of the Invention
This invention relates to improved soap-based lubricants, more particularly, chain conveyor lubricants and even more particularly, to aqueous compositions for such application containing fatty acid soaps.
2. Description of the Prior Art
In breweries, soft drink bottling operations and food processing plants, conveyors are used to move the bottles, jars, cans, and the like along the line. In order to keep the conveyor chains clean and provide lubrication, it is customary to use a lubricant such as an aqueous soap- based lubricant. These compositions also include chelating agents to prevent precipitation of calcium and magnesium soaps. These lubricants are generally manufactured and sold as concentrates which must then- be diluted to in general about 1:100 with tap water at the point of use.
However, prior to dilution, the concentrate is fed through proportioning pumps or injectors whereby it is important that the concentrated soaps which tend to be very viscous have their viscosity reduced. In the prior art, materials have been added to reduce viscosity of the concentrated lubricants, more particularly, propylene glycol, isopropyl alcohol, eaprie
(decanoic) acid and coconut fatty acid. Also, some surfactants such as alkoxylated alcohols have been employed to reduce viscosity. However, antifreezes such as propylene glycol and isopropyl alcohol, while they may reduce viscosity to some extent, also may reduce lubricity. Natural materials such as eaprie (decanoic) acid and coconut fatty acid may reduce viscosity but lubricity is slightly reduced and they often require more chelating agents to handle the additional precipitates when diluted with normal tap water. Further, lubricants which contain eaprie or coconut
fatty acid tend to cause an objectionable black film on the bottoms of the bottles and other containers passing along the conveyor. The surfac¬ tants generally have the disadvantages of higher costs, and an excess of surfactant sometimes cleans the metal surface to a point where lubricity may be lost completely.
Accordingly, it is the purpose of this invention to provide an aqueous soap-based lubricant particularly a lubricant for chain conveyors which has low viscosity, good lubricity, which does not blacken the bottoms of the bottles and cans or other containers when employed on conveyors and which does not require extra chelating agents to handle the additional precipitates when diluted with normal tap water.
Statement of Relevant Patents To the best of applicants' knowledge, the following patents are the ones most relevant to a determination of patentability:
References U.S. Patent No. Inventor Issue Date Assignee
3,923,671 ' Knepp 12/02Λ975 Aluminum Co. of Amer.
3,663,438 Smith et al 05/16/1972 Shell Oil Co.
2,863,847 Morway 12/09/1958 Esso
3,923,671, Knepp - Discloses a metal working lubricant which comprises a combination of a carboxylic acid with other lubricating agents, i.e., carboxylic acid esters, emulsifiers and mineral oil. The carboxylic acid useful in the invention contains at least 12 carbon atoms. 3,663,438, Smith - Discloses grease compositions comprising a mineral lubricating oil thickened to grease consistency having incorporated therein minor amounts of a phenothiazine-type inhibitor and a polyester of a C,_2Q alcohol and a C, ,„ carboxylic acid. Among the carboxylic acids listed are decanoic acid.
2,863,847, Morway - Discloses lubricating compositions consisting of hydrous mixtures of metal salts of low molecular weight carboxylic acids and moderate molecular weight carboxylic acids and to sols, gels and greases containing the same. Among the intermediate molecular weight
OM
monocarboxylie acids disclosed are decanoic (eaprie).
The two latter patents do not disclose decanoic acid by itself as a grease additive but only compounds thereof. Further, there is no disclosure in either reference of even a compound of neodecanoic acid. .
Summary of the Invention In accordance with this invention, there is provided in an aqueous water-soluble soap lubricant concentrate, most particularly for lubricating continuously moving conveyor systems, the improvement comprising the inclusion therein of neodecanoic acid in amount from about 0.1 to 50.0 percent by weight of the concentrate. The concentrate, when diluted with water, is then ready for use in a lubricating composition. Description of the Preferred Embodiments The typical chain conveyor lubricant for convenience and economy in transporting and storing is manufactured and sold as a concen¬ trate which is then diluted with water in proportions by volume of from about 1:50 parts concentrate to water to about 1:500 parts concentrate to water for usage. The lubricant concentrate typically contains about 2 to 40 percent by weight water-soluble fatty acid soap, about 0 to 15 percent by weight chelating agent, about 0 to 45 percent by weight surface active agent which may be either anionie, nonionic or both, and about 20 to 80 percent by weight water. Usually, it is more preferred that the concentrate contain by weight about 4 to 20 percent water-soluble fatty acid soap, about 2 to 15 percent chelating agent, about 1 to 20 percent surface active agent and about 30 to 70 percent water.
According to this invention, neodecanoic acid is added to the foregoing composition to achieve the purposes of the present invention. Typically, the neodecanoic acid is added in an amount from about 0.1 to 50 percent by weight of the concentrate, more preferably, from about o.5 to 5.0 percent by weight of the concentrate, and most preferably, about 1.0 to 3.0 percent by weight concentrate. While decanoic, also known as eaprie, acid has been well known in the art for years, the neoacids, which are synthetic highly-branched organic acids, are relatively new. The "neo" structure is generally considered to be as follows:
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_ _
c — c — c
I c
Commercially produced neodecanoic acid is composed of a number of C.Q isomers characterized by the presence of the above , structure but in varying locations along the chain. It is generally a liquid with a low freezing point, i.e., less than -40° C, whereas decanoic (eaprie) acid is a solid melting at 31.4° C. Neodecanoic acid is synthesized starting with an olefin of mixed nonenes (at equilibrium) yielding a C,Q neoacid containing many isomers. This very highly branched and multi-isomer acid combination yields a liquid C]0 neoacid with a typical hydrocarbon- type odor. A typical structure and isomer distribution for neodecanoic acid is set forth below.
Typical Isomer Distribution for Neodecanoic Acid
χ
R C COOH
3 I ' R2
Alkyl group 96 Rj and R„ = methyl 31
Ε = methyl; R2 methyl 67
R, and „ > methyl 2
R, always > methyl
This product is described in the article entitled "Neoacids: Synthetic Highly Branched Organic Acids", Journal of American Oil Chemists
Society, Vol. 55, No. 4, pp. 342A to 345A (1978).
It is preferred to employ as the chelating agent salts of ethylene diamine tetraacetic acid. These sequestering agents may be added to the composition in the form of the salts or the acid may be added along with a sufficient amount of metallic hydroxide or alkanolamine to neutralize the acids. A preferred chelating agent is the tetrasodium
salt of ethylene diamine tetraacetic acid.
Any chelating agent which will complex calcium and magnesium ions from water may be employed in this invention. Additional suitable chelating agents are trans-l,2-diaminocyclohexane tetraacetic acid monohy- drate, diethylene triamine pentaacetic acid, sodium salt of nitrilotriacetic acid, pentasodium salt of N-hydroxy ethylene diamine triacetic acid, trisodium salt of N,N-di(beta-hydroxyethyl) glycine, and sodium salt of sodium glucoheptonate.
Where the formula is diluted in tap water, conventional metallic soap dispersions may be necessary or desirable in addition to the chelating agents.
For the sake of simplicity in formulating the composition, instead of adding fatty acid soap as such, it is preferred to simply add fatty acid in amount from about 2 to 30 weight percent for the broad composition or 4 to 15 percent by weight of the preferred composition and then add a sufficient amount of an alkali metal (from the first column of the periodic table) hydroxide, ammonium hydroxide or an alkanolamine to neutralize the fatty acid to produce a fatty acid soap. Where the chelating agent is also added in the acid form, the foregoing hydroxide or alkanolamine is added in sufficient amount to neutralize both the chelating agent and the fatty acid. Preferred fatty acids for this purpose are tall oil fatty acids with low rosin content of about 0.5 to about 0.9 percent by weight and which generally comprise approximately 52 percent by weight oleic acid, 45 percent by weight linoleic acid, 1 percent by weight linolenic acid and 2.3 percent by weight saturated acid. Coconut oil fatty acids generally comprised of 50 percent lauric, 20 percent myristic, 10 percent oleic, 10 percent palmitic, 8 percent of other saturated fatty acids, and about 2 percent unsaturated fatty acids are also desirable for this purpose. Additional useful fatty acids include those derived from tallow, soya beans, corn, cotton seed, palm, and blends or hydrogenated forms of the basic type of fatty acid to give desired characteristics such as low solubilization temperature, viscosity and reduced corrosion tendency.
Sodium, ammonium or potassium hydroxide and mono, di, and triethanolamine or isopropanolamine are the preferred source used in neutralizing and converting fatty acids to soaps. Potassium hydroxide
and monethanolamine are preferred for their ability to produce compounds with a pH and foam generating capacity suitable for conveyor lubricants.
Conventional anionic and nonionic surface active agents are often also included in the composition. Anionic surface active agents which may be employed include linear alkyl benzene sulfonic acids, alpha- olefin sulfonates, alkyl δiphenyl oxide disulfonates, sodium N-methyl- N-alkyl-taurate, alkyl sulf onated amides, di(2-ethylhexyl) sulfosuccinate, dioctyl sodium sulfosuccinate, sodium sulfonate of oleic acid, anionic phosphate esters, alkyl ether sulf ates, alkyl polyethyleneoxy esters, alcohol sulfates such as sodium lauryl sulfonate, the product of ehlorosulfonation of paraffin hydrocarbons, e.g., octadecenyl sulfonate and the condensate of a fatty acid chloride with an amine.
. The nonionic surface active agents which are advantageously employed in the compositions of the invention are generally the polyoxy- alkylene adducts of hydrophobic bases wherein the oxygen/carbon atom ratio in the oxyalkylene portion of the molecule is greater than 0.40. Those compositions which are condensed with hydrophobic bases to provide a polyoxyalkylene portion having an oxygen/carbon atom ratio greater than 0.40 include ethylene oxide, butadiene dioxide and glycidol, mixtures of these alkylene oxides with each other and with minor amounts of propylene oxide, butylene oxide, amylene oxide, styrene oxide, and other higher molecular weight alkylene oxides. Ethylene oxide, for example, is condensed with the hydrophobic base in an amount sufficient to impart water dispersi- bility or solubility and surface active properties to the molecule being prepared. The exact amount of ethylene oxide condensed with the hydro- phobic base will depend upon the chemical characteristics of the base employed and is readily apparent to those of ordinary skill in the art relating to the synthesis of oxyalkylene surfactant condensates.
Typical hydrophobic bases which can be condensed with ethylene oxide in order to prepare nonionic surface active agents include mono- and polyalkyl phenols, polyoxypropylene condensed with a base having from about 1 to 6 carbon atoms and at least one reactive hydrogen atom, fatty acids, fatty amines, fatty amides and fatty alcohols. The hydrocarbon ethers such as the benzyl or lower alkyl ether of the polyoxy- ethylene surfactant condensates are also advantageously employed in
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the compositions of the invention.
Among the suitable nonionic surface active agents are the polyoxyethylene condensates of alkyl phenols having from about 6 to 20 carbon atoms in the alkyl portion and from about 5 to 30 ethenoxy groups in the polyoxyethylene radical. The alkyl substituent on the aromatic nucleus may be octyl, diamyl, n-dodeeyl, polymerized propylene such as propylene tetramer and trimer, isooctyl, nonyl, etc. The benzyl ethers of the polyoxyethylene condensates of monoalkyl phenols impart good properties to the compositions of the invention and a typical product corresponds to the formula:
C8H17 J (°CH2CH2)15OCH2C6H5
Higher polyalkyl oxyethylated phenols corresponding to the formula:
wherein R is hydrogen or an alkyl radical having from about 1 to 12 carbon atoms, R 1 and R 2 are alkyl radicals having from about 6 to 16 carbon atoms and n has a value from about 10 to 40, are also suitable as nonionic surface active agents. A typical oxyethylated polyalkyl phenol is dinonyl phenol condensed with 14 moles of ethylene oxide. Other suitable nonionic surface active agents are eogeneric mixtures of conjugated polyoxyalkylene compounds containing in their structure at least one hydrophobic oxyalkylene chain in which the oxygen/car¬ bon atom ratio does not exceed 0.40 and at least one hydrophilie oxyalkylene chain in which the oxygen/carbon atom ratio is greater than 0.40. Polymers of oxyalkylene groups obtained from propylene oxide, butylene oxide, amylene oxide, styrene oxide, mixtures of such oxyalkylene groups with each other and with minor amounts of polyoxy¬ alkylene groups obtained from ethylene oxide, butadiene dioxide, and glyeidol are illustrative of hydrophobic oxyalkylene chains having an oxygen/carbon atom ratio not exceeding 0.40. Polymers of oxyalkylene
groups obtained from ethylene oxide, butadiene dioxide, glycidol, mixtures of such oxyalkylene groups with each other and with minor amounts of oxyalkylene groups obtained from propylene oxide, butylene oxide, amylene oxide and styrene oxide are illustrative of hydrophilic oxyalkylene chains having an oxygen/carbon atom ratio greater than 0.40.
Further suitable nonionic surface active agents are the polyoxyethylene esters of higher fatty acids having from about 8 to 22 carbon atoms in the acyl group and from about 8 to 30 ethenoxy units in the oxyethylene portion. Typical products are the polyoxyethylene adducts of tall oil, rosin acids, lauric, stearic and oleic acids and the like. Additional nonionic surface active agents are the polyoxyethylene condensates of higher fatty acid amines and amides having from about 8 to 22 carbon atoms in the fatty alkyl or acyl group and about 10 to 30 ethenoxy units in the oxyethylene portion. Illustrative products are coconut oil fatty acid amines and amides condensed with about 10 to 30 moles of ethylene oxide.
Other suitable polyoxyalkylene nonionic surface active agents are the alkylene oxide adducts of higher aliphatic alcohols and thioalcohols having from about 8 to 22 carbon atoms in the aliphatic portion and about 3 to 50 in the oxyalkylene portion. Typical products are synthetic fatty alcohols, such as n-deeyl, n-undecyl, n-dodecyl, n- trideeyl, n-tetradecyl, n-hexadecyl, n-octadecyl and mixtures thereof condensed with 3 to 50 moles of the ethylene oxide, a mixture of normal fatty alcohols condensed with 8 to 20 moles of ethylene oxide and capped with benzyl halide or an alkyl halide, a mixture of normal fatty alcohols condensed with 10 to 30 moles of a mixture of ethylene and propylene oxides, a mixture of several fatty alcohols condensed sequentially with 2 to 20 moles of ethylene oxide and 3 to 10 moles of propylene oxide, in either order; or a mixture of normal fatty alcohols condensed with a mixture of propylene and ethylene oxides, in which the oxygen/carbon atom ratio is less than 0.40 followed by a mixture of propylene and ethylene oxides in which the oxygen/carbon atom ratio is greater than 0.40 or a linear secondary alcohol condensed with 3 to 30 moles of ethylene oxide, or a linear secondary alcohol condensed with a mixture of propylene and
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9 -
ethylene oxides, or a linear secondary alcohol condensed with a mixture of ethylene, propylene, and higher alkylene oxides.
The compositions of this invention are prepared by standard well-known open kettle mixing techniques known in the industry. The practice of this invention is illustrated by the examples
• given below. Unless otherwise noted, temperature is expressed in degrees Centigrade and parts and percentages are by weight.
Laboratory tests were conducted to compare viscosities, lubricities, and maximum dilutions in terms of effectiveness value of neodecanoic acid with various materials previously used in the industry as viscosity reducers. The results are shown in the Table below.
The viscosities were run with a Brookfield viscosity meter at 25° C. Viscosities below 100 cps are considered ideal. Maximum dilution was determined by adding 6 grain water hardness tap water at 20° C to 1 gram of concentrated lubricant until the solution becomes cloudy. The friction-power coefficient, which is a measure of lubricity, is determined on a 5-foot section of an actual industrial bottle conveyor chain. The unit is powered by a DC motor and a Servodyne control unit from Cole- Parmer Instrument Company. The Servodyne unit measures motor torque. A Varian Recorder, Model 9176, then records the changes in power as the lubricant is added to the conveyor chain. A load consists of 10 to 12 bottles filled with water and the lubricated chain slides under the restricted bottles. The friction-power coefficient indicates the average recorded value during a 30-minute run using a dilution with tap water at 1:80. The effectiveness value (E) at a specific concentration of these materials is determined with the following equation:
E = 100 x D
V x F
Where
E = Effectiveness value
V = Viscosity cps
F = Friction-power coefficient as measured on lab lube tester D = Maximum dilution (with 6 grain tap water)
In order to compare a series of viscosity reducers, a standard water-based formula was prepared as follows:
Ingredients Parts by Weight Water 74
Tetrasodium Salt of Ethylenediamine- tetraacetic acid 4
Tall Oil Fatty Acid 12 KOH, 45% aqueous solution 6
Surfactant* 1
97
* The surfactant was an oxyalkylated alcohol from 22 percent by weight Ci2-Tϊ &ttv a 0000!? 47 percent by weight ethylene oxide and 31 percent by weight propylene oxide.
To 97 parts by weight of the above formula, 2 parts by weight viscosity reducing agent was added. One part by weight of either water or 45 percent aqueous KOH solution or mixture thereof was added in order to maintain the same desired pH of 10.0.
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F
Viscosity V D Friction E Reducing Agent Viscosity Max. Dilution Power Effectiveness 2% by wt. cps 6 grain water Coefficient Value
Water 10,000 1:85 5.40 1.60
Capric acid 125 1:90 5.55 129.70
Neodecanoic acid 20 1:100 5.48 912.40
I
-ti Coconut fatty acid 9,600 1:90 5.60 1.67
I
Surfactant* 680 1:100 5.65 26.00
Propylene glycol 2,900 1:110 5.55 6.80
Isopropyl alcohol 1,200 1:110 5.60 16.40
* The surfactant was an oxyalkylated alcohol from 22 percent by weight C12_,,- fatty alcohol, 47 percent by weight ethylene oxide and 31 percent by weight propylene oxide.
o ©
© O
O
A further study was made to compare viscosity reducing characteristics of neodecanoic acid to eaprie acid, the results of which are shown in Figures 1 and 2 of the drawing wherein:
Figure 1 shows the viscosities for a water-based formula, similar to that set forth above, with neodecanoic acid and with eaprie
(decanoic) acid in varying amounts up to 5 percent by weight of the concentrate. The formula consisted of by weight 12 percent tall oil fatty acid, 4 percent tetrasodium salt of ethylenediamine tetraacetic acid and 1 percent surfactant. Sufficient KOH and water were added to maintain a pH of 10 and to make up the balance for a total of 100 percent.
Figure 2 shows the viscosities with neodecanoic acid and with eaprie (decanoic) acid in varying amounts up to 6 percent by weight of the concentrate for another more viscous formula consisting of by weight 18 percent tall oil fatty acid, 4 percent tetrasodium salt of ethylenediamine tetraacetic acid and 1 percent surfactant. Sufficient
KOH and water were added to maintain a pH of 10.0 and to make up the balance for a total of 100 percent. Higher concentrations of tall oil fatty acid produce much higher viscosities and the viscosity reducing character¬ istics of neodecanoic acid become more apparent in the more eoneen- trated products.
The foregoing examples and methods have been described in the foregoing specification for purpose of illustration. Many other modifications will naturally suggest themselves to those skilled in the art based on this disclosure. These are intended to be comprehended as being within the scope of this invention.
-BURE
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Claims (9)
1. In an aqueous water-soluble soap lubricant concentrate, the improvement comprising the inclusion therein of neodecanoic acid in amount from about 0.1 to 50.0 percent by weight of said concentrate.
2. The improvement of claim 1 wherein said concentrate is for a continuously moving conveyor system lubricant.
3. The improvement of claim 1 wherein said concentrate contains a water-soluble fatty acid soap and a chelating agent.
4. The improvement of claim 3 wherein said concentrate also includes a surfactant.
5. The improvement of claim 3 wherein said concentrate contains about 2 to 40 percent by weight fatty acid soap, about 0 to 15 percent by weight chelating agent, about 0 to 45 percent by weight surface active agent, and about 20 to 80 percent by weight water.
6. The improvement of claim 5 wherein the fatty acid soap is obtained by incorporating in said concentrate a fatty acid in an amount from about 2 to 30 weight percent along with an agent selected from the group consisting of alkali metal hydroxide, ammonium hydroxide, and alkanol-amines in amounts sufficient to react with the fatty acid to produce the fatty acid soap.
7. The improvement of claim 6 wherein said fatty acid is tall oil fatty acid, said agent to react with the fatty acid is potassium hydroxide, said chelating agent is tetrasodium salt of ethylene diamine tetraacetic acid, and said surface active agent is an oxyalkylated fatty alcohol from 22 percent by weight C,2_1 £. fatty alcohol, 47 percent by weight ethylene oxide and 31 percent by weight propylene oxide.
"BUREAU
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8. A lubricating composition consisting essentially of the concentrate according to claim 5 and water in a volumetric proportion of concentrate to water of about 1:50 to about 1:500.
9. A lubricating composition consisting essentially of the concentrate according to claim 6 and water in a volumetric proportion of concentrate to water of about 1:50 to about 1:500.
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US06/051,008 US4274973A (en) | 1979-06-22 | 1979-06-22 | Aqueous water-soluble soap lubricant concentrates and aqueous lubricants containing same |
US051008 | 1979-06-22 | ||
PCT/US1980/000757 WO1981000014A1 (en) | 1979-06-22 | 1980-06-19 | Improved aqueous soap-based lubricant composition |
Publications (2)
Publication Number | Publication Date |
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AU6123780A AU6123780A (en) | 1981-01-14 |
AU535697B2 true AU535697B2 (en) | 1984-03-29 |
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ID=26728952
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Application Number | Title | Priority Date | Filing Date |
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AU61237/80A Ceased AU535697B2 (en) | 1979-06-22 | 1980-06-19 | Improved aqueous soap-based lubricant composition |
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AU (1) | AU535697B2 (en) |
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1980
- 1980-06-19 AU AU61237/80A patent/AU535697B2/en not_active Ceased
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