EP0819754B1 - Beta-dithiophosphorilated propionic acid in lubricants - Google Patents
Beta-dithiophosphorilated propionic acid in lubricants Download PDFInfo
- Publication number
- EP0819754B1 EP0819754B1 EP97810446A EP97810446A EP0819754B1 EP 0819754 B1 EP0819754 B1 EP 0819754B1 EP 97810446 A EP97810446 A EP 97810446A EP 97810446 A EP97810446 A EP 97810446A EP 0819754 B1 EP0819754 B1 EP 0819754B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- tert
- butyl
- bis
- composition according
- lubricants
- 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.)
- Expired - Lifetime
Links
- 239000000314 lubricant Substances 0.000 title claims description 30
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 title description 3
- 235000019260 propionic acid Nutrition 0.000 title description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 title 2
- -1 2-ethylhexyl Chemical group 0.000 claims description 52
- 239000000203 mixture Substances 0.000 claims description 39
- 150000001875 compounds Chemical class 0.000 claims description 20
- 239000003921 oil Substances 0.000 claims description 20
- 239000000654 additive Substances 0.000 claims description 18
- 239000012530 fluid Substances 0.000 claims description 17
- 238000005555 metalworking Methods 0.000 claims description 12
- 239000000446 fuel Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 6
- 239000011707 mineral Substances 0.000 claims description 6
- 239000003963 antioxidant agent Substances 0.000 claims description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 239000002270 dispersing agent Substances 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 239000003112 inhibitor Substances 0.000 claims description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 235000013311 vegetables Nutrition 0.000 claims description 4
- 239000003599 detergent Substances 0.000 claims description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 2
- 239000007866 anti-wear additive Substances 0.000 claims description 2
- 239000002199 base oil Substances 0.000 claims description 2
- 239000004519 grease Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 230000005540 biological transmission Effects 0.000 claims 1
- 150000002148 esters Chemical class 0.000 description 15
- 239000002253 acid Substances 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- 239000007983 Tris buffer Substances 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 6
- 229910052717 sulfur Inorganic materials 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 5
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 4
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 4
- BVUXDWXKPROUDO-UHFFFAOYSA-N 2,6-di-tert-butyl-4-ethylphenol Chemical compound CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BVUXDWXKPROUDO-UHFFFAOYSA-N 0.000 description 4
- SLUKQUGVTITNSY-UHFFFAOYSA-N 2,6-di-tert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLUKQUGVTITNSY-UHFFFAOYSA-N 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 4
- LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 4
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 125000005037 alkyl phenyl group Chemical group 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 235000006708 antioxidants Nutrition 0.000 description 4
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 4
- 239000011575 calcium Substances 0.000 description 4
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000003925 fat Substances 0.000 description 4
- 235000019197 fats Nutrition 0.000 description 4
- 239000012208 gear oil Substances 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000003760 tallow Substances 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- GZIFEOYASATJEH-VHFRWLAGSA-N δ-tocopherol Chemical compound OC1=CC(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 GZIFEOYASATJEH-VHFRWLAGSA-N 0.000 description 4
- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical compound S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 description 3
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- JWUXJYZVKZKLTJ-UHFFFAOYSA-N Triacetonamine Chemical compound CC1(C)CC(=O)CC(C)(C)N1 JWUXJYZVKZKLTJ-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- 239000010720 hydraulic oil Substances 0.000 description 3
- 239000003879 lubricant additive Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- ZQMPWXFHAUDENN-UHFFFAOYSA-N n,n'-bis(2-methylphenyl)ethane-1,2-diamine Chemical compound CC1=CC=CC=C1NCCNC1=CC=CC=C1C ZQMPWXFHAUDENN-UHFFFAOYSA-N 0.000 description 3
- 229920013639 polyalphaolefin Polymers 0.000 description 3
- 150000004672 propanoic acids Chemical class 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 239000008158 vegetable oil Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 150000000178 1,2,4-triazoles Chemical class 0.000 description 2
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 2
- ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 2
- NRKKTPXKEYHVCZ-UHFFFAOYSA-N 1-(1-butoxyethyl)-1,2,4-triazole Chemical compound CCCCOC(C)N1C=NC=N1 NRKKTPXKEYHVCZ-UHFFFAOYSA-N 0.000 description 2
- BUGAMLAPDQMYNZ-UHFFFAOYSA-N 1-(2,4,4-trimethylpentan-2-yl)-10h-phenothiazine Chemical class S1C2=CC=CC=C2NC2=C1C=CC=C2C(C)(C)CC(C)(C)C BUGAMLAPDQMYNZ-UHFFFAOYSA-N 0.000 description 2
- KSYAJTVGOSTFLK-UHFFFAOYSA-N 1-(nonoxymethyl)benzotriazole Chemical compound C1=CC=C2N(COCCCCCCCCC)N=NC2=C1 KSYAJTVGOSTFLK-UHFFFAOYSA-N 0.000 description 2
- VMDYMJSKWCVEEB-UHFFFAOYSA-N 1-[3,5-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyl]-1,3,5-triazinan-1-yl]-3-(3,5-ditert-butyl-4-hydroxyphenyl)propan-1-one Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)N2CN(CN(C2)C(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 VMDYMJSKWCVEEB-UHFFFAOYSA-N 0.000 description 2
- IQYDSMJRFWLGKA-UHFFFAOYSA-N 1-[bis(2-hydroxyethyl)amino]-3-(4-nonylphenoxy)propan-2-ol Chemical compound CCCCCCCCCC1=CC=C(OCC(O)CN(CCO)CCO)C=C1 IQYDSMJRFWLGKA-UHFFFAOYSA-N 0.000 description 2
- PIDRVLYMNGNSPO-UHFFFAOYSA-N 1-methyl-2-[(1-methylimidazol-2-yl)-octoxymethyl]imidazole Chemical compound N=1C=CN(C)C=1C(OCCCCCCCC)C1=NC=CN1C PIDRVLYMNGNSPO-UHFFFAOYSA-N 0.000 description 2
- BBRHQNMMUUMVDE-UHFFFAOYSA-N 1-n,2-n-diphenylpropane-1,2-diamine Chemical compound C=1C=CC=CC=1NC(C)CNC1=CC=CC=C1 BBRHQNMMUUMVDE-UHFFFAOYSA-N 0.000 description 2
- JUHXTONDLXIGGK-UHFFFAOYSA-N 1-n,4-n-bis(5-methylheptan-3-yl)benzene-1,4-diamine Chemical compound CCC(C)CC(CC)NC1=CC=C(NC(CC)CC(C)CC)C=C1 JUHXTONDLXIGGK-UHFFFAOYSA-N 0.000 description 2
- ZJNLYGOUHDJHMG-UHFFFAOYSA-N 1-n,4-n-bis(5-methylhexan-2-yl)benzene-1,4-diamine Chemical compound CC(C)CCC(C)NC1=CC=C(NC(C)CCC(C)C)C=C1 ZJNLYGOUHDJHMG-UHFFFAOYSA-N 0.000 description 2
- BJLNXEQCTFMBTH-UHFFFAOYSA-N 1-n,4-n-di(butan-2-yl)-1-n,4-n-dimethylbenzene-1,4-diamine Chemical compound CCC(C)N(C)C1=CC=C(N(C)C(C)CC)C=C1 BJLNXEQCTFMBTH-UHFFFAOYSA-N 0.000 description 2
- APTGHASZJUAUCP-UHFFFAOYSA-N 1-n,4-n-di(octan-2-yl)benzene-1,4-diamine Chemical compound CCCCCCC(C)NC1=CC=C(NC(C)CCCCCC)C=C1 APTGHASZJUAUCP-UHFFFAOYSA-N 0.000 description 2
- PWNBRRGFUVBTQG-UHFFFAOYSA-N 1-n,4-n-di(propan-2-yl)benzene-1,4-diamine Chemical compound CC(C)NC1=CC=C(NC(C)C)C=C1 PWNBRRGFUVBTQG-UHFFFAOYSA-N 0.000 description 2
- AIMXDOGPMWDCDF-UHFFFAOYSA-N 1-n,4-n-dicyclohexylbenzene-1,4-diamine Chemical compound C1CCCCC1NC(C=C1)=CC=C1NC1CCCCC1 AIMXDOGPMWDCDF-UHFFFAOYSA-N 0.000 description 2
- ZRMMVODKVLXCBB-UHFFFAOYSA-N 1-n-cyclohexyl-4-n-phenylbenzene-1,4-diamine Chemical compound C1CCCCC1NC(C=C1)=CC=C1NC1=CC=CC=C1 ZRMMVODKVLXCBB-UHFFFAOYSA-N 0.000 description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 2
- TUYBEVLJKZQJPO-UHFFFAOYSA-N 19-(3,5-ditert-butyl-4-hydroxyphenyl)heptatriacontan-19-ylphosphonic acid Chemical compound CCCCCCCCCCCCCCCCCCC(CCCCCCCCCCCCCCCCCC)(P(O)(O)=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 TUYBEVLJKZQJPO-UHFFFAOYSA-N 0.000 description 2
- CDWOTAMGTNNLHY-UHFFFAOYSA-N 19-(3-tert-butyl-4-hydroxy-5-methylphenyl)heptatriacontan-19-ylphosphonic acid Chemical compound CCCCCCCCCCCCCCCCCCC(CCCCCCCCCCCCCCCCCC)(P(O)(O)=O)C1=CC(C)=C(O)C(C(C)(C)C)=C1 CDWOTAMGTNNLHY-UHFFFAOYSA-N 0.000 description 2
- VDVUCLWJZJHFAV-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1 VDVUCLWJZJHFAV-UHFFFAOYSA-N 0.000 description 2
- UUAIOYWXCDLHKT-UHFFFAOYSA-N 2,4,6-tricyclohexylphenol Chemical compound OC1=C(C2CCCCC2)C=C(C2CCCCC2)C=C1C1CCCCC1 UUAIOYWXCDLHKT-UHFFFAOYSA-N 0.000 description 2
- LXWZXEJDKYWBOW-UHFFFAOYSA-N 2,4-ditert-butyl-6-[(3,5-ditert-butyl-2-hydroxyphenyl)methyl]phenol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)C)C(C)(C)C)O)=C1O LXWZXEJDKYWBOW-UHFFFAOYSA-N 0.000 description 2
- DXCHWXWXYPEZKM-UHFFFAOYSA-N 2,4-ditert-butyl-6-[1-(3,5-ditert-butyl-2-hydroxyphenyl)ethyl]phenol Chemical compound C=1C(C(C)(C)C)=CC(C(C)(C)C)=C(O)C=1C(C)C1=CC(C(C)(C)C)=CC(C(C)(C)C)=C1O DXCHWXWXYPEZKM-UHFFFAOYSA-N 0.000 description 2
- FLLRQABPKFCXSO-UHFFFAOYSA-N 2,5-ditert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C=C1C(C)(C)C FLLRQABPKFCXSO-UHFFFAOYSA-N 0.000 description 2
- YEWBOZCFGXOUQW-UHFFFAOYSA-N 2,6,7-trioxa-1-phosphabicyclo[2.2.2]octan-4-ylmethanol Chemical compound C1OP2OCC1(CO)CO2 YEWBOZCFGXOUQW-UHFFFAOYSA-N 0.000 description 2
- LKALLEFLBKHPTQ-UHFFFAOYSA-N 2,6-bis[(3-tert-butyl-2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound OC=1C(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=CC(C)=CC=1CC1=CC(C)=CC(C(C)(C)C)=C1O LKALLEFLBKHPTQ-UHFFFAOYSA-N 0.000 description 2
- FRAQIHUDFAFXHT-UHFFFAOYSA-N 2,6-dicyclopentyl-4-methylphenol Chemical compound OC=1C(C2CCCC2)=CC(C)=CC=1C1CCCC1 FRAQIHUDFAFXHT-UHFFFAOYSA-N 0.000 description 2
- JBYWTKPHBLYYFJ-UHFFFAOYSA-N 2,6-ditert-butyl-4-(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 JBYWTKPHBLYYFJ-UHFFFAOYSA-N 0.000 description 2
- SCXYLTWTWUGEAA-UHFFFAOYSA-N 2,6-ditert-butyl-4-(methoxymethyl)phenol Chemical compound COCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SCXYLTWTWUGEAA-UHFFFAOYSA-N 0.000 description 2
- UDFARPRXWMDFQU-UHFFFAOYSA-N 2,6-ditert-butyl-4-[(3,5-ditert-butyl-4-hydroxyphenyl)methylsulfanylmethyl]phenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CSCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 UDFARPRXWMDFQU-UHFFFAOYSA-N 0.000 description 2
- QHPKIUDQDCWRKO-UHFFFAOYSA-N 2,6-ditert-butyl-4-[2-(3,5-ditert-butyl-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(C(C)(C)C=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 QHPKIUDQDCWRKO-UHFFFAOYSA-N 0.000 description 2
- FURXDDVXYNEWJD-UHFFFAOYSA-N 2,6-ditert-butyl-4-[[4-(3,5-ditert-butyl-4-hydroxyanilino)-6-octylsulfanyl-1,3,5-triazin-2-yl]amino]phenol Chemical compound N=1C(NC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=NC(SCCCCCCCC)=NC=1NC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 FURXDDVXYNEWJD-UHFFFAOYSA-N 0.000 description 2
- JMCKNCBUBGMWAY-UHFFFAOYSA-N 2,6-ditert-butyl-4-[[4-(3,5-ditert-butyl-4-hydroxyphenoxy)-6-octylsulfanyl-1,3,5-triazin-2-yl]oxy]phenol Chemical compound N=1C(OC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=NC(SCCCCCCCC)=NC=1OC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 JMCKNCBUBGMWAY-UHFFFAOYSA-N 0.000 description 2
- DEHILEUXPOWXIS-UHFFFAOYSA-N 2-(2,5-ditert-butyl-4-hydroxyphenyl)propan-2-ylphosphonic acid Chemical compound CC(C)(C)C1=CC(C(C)(C)P(O)(O)=O)=C(C(C)(C)C)C=C1O DEHILEUXPOWXIS-UHFFFAOYSA-N 0.000 description 2
- BNGLZYYFFZFNDJ-UHFFFAOYSA-N 2-(2-heptadec-1-enyl-4,5-dihydroimidazol-1-yl)ethanol Chemical compound CCCCCCCCCCCCCCCC=CC1=NCCN1CCO BNGLZYYFFZFNDJ-UHFFFAOYSA-N 0.000 description 2
- LBOGPIWNHXHYHN-UHFFFAOYSA-N 2-(2-hydroxy-5-octylphenyl)sulfanyl-4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C(SC=2C(=CC=C(CCCCCCCC)C=2)O)=C1 LBOGPIWNHXHYHN-UHFFFAOYSA-N 0.000 description 2
- QLMGIWHWWWXXME-UHFFFAOYSA-N 2-(3,5-ditert-butyl-4-hydroxyphenyl)acetic acid Chemical compound CC(C)(C)C1=CC(CC(O)=O)=CC(C(C)(C)C)=C1O QLMGIWHWWWXXME-UHFFFAOYSA-N 0.000 description 2
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- 239000011777 magnesium Substances 0.000 description 1
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- 238000004519 manufacturing process Methods 0.000 description 1
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- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
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- 238000003756 stirring Methods 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
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- SHEXSXZCZQBTFI-UHFFFAOYSA-N tridecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)-2-sulfanylpropanoate Chemical compound CCCCCCCCCCCCCOC(=O)C(S)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SHEXSXZCZQBTFI-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- IKXFIBBKEARMLL-UHFFFAOYSA-N triphenoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=S)OC1=CC=CC=C1 IKXFIBBKEARMLL-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- SMVBWTKCDCPTQG-UHFFFAOYSA-N tris[2-(7-methyloctyl)phenoxy]-sulfanylidene-$l^{5}-phosphane Chemical compound CC(C)CCCCCCC1=CC=CC=C1OP(=S)(OC=1C(=CC=CC=1)CCCCCCC(C)C)OC1=CC=CC=C1CCCCCCC(C)C SMVBWTKCDCPTQG-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
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- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/26—Organic compounds containing phosphorus
- C10L1/2633—Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond)
- C10L1/265—Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond) oxygen and/or sulfur bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/08—Use of additives to fuels or fires for particular purposes for improving lubricity; for reducing wear
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
- C10M137/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
- C10M137/04—Phosphate esters
- C10M137/10—Thio derivatives
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Definitions
- the present invention relates to compositions containing a lubricant (preferably an industrial oil or a grease), a metalworking or a Hydraulic fluid and at least one ⁇ -dithiophosphorylated propionic acid Formula I described below.
- a lubricant preferably an industrial oil or a grease
- metalworking or a Hydraulic fluid preferably an industrial oil or a grease
- at least one ⁇ -dithiophosphorylated propionic acid Formula I described below preferably an industrial oil or a grease
- Additives are added to modern lubricants, which perform tasks such as high-pressure and wear protection, corrosion protection and antioxidation effects [WJ Bartz (Editor), et al., "Additives for lubricants” (expert-Verlag 1994)].
- Zinc dialkyldithiophosphates which combine antioxidative and high-pressure and wear protection effects, are of particular importance.
- efforts have been made to largely replace these heavy metal additives with metal-free compounds, because this is environmentally friendly and has a positive effect on the service life of the exhaust gas catalysts of internal combustion engines.
- Type of ester are available under the trade name lrgalube TM 63.
- US 4,333,841 dithiophosphorylated mercaptoacetic acids and their salts are described as lubricant additives.
- R 1 and R 2 are, independently of one another, C 3 -C 18 alkyl, C 5 -C 6 cycloalkyl or C 7 -C 18 alkylphenyl.
- R 1 and R 2 are particularly preferably i-propyl, i-butyl or 2-ethylhexyl, and R 3 is hydrogen.
- IR 1 and R 2 are C 3 -C 18 -alkyl in the above formula, these are branched or unbranched radicals. Examples include propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, isopentyl, hexyl, heptyl, 3-heptyl, octyl, 2-ethylhexyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl , Heptadecyl, octadecyl, 2-ethylbutyl, 1-methylpentyl, 1,3-dimethylbutyl, 1,1,3,3-tetramethylbutyl, 1-methylhexyl, isoheptyl, 1-methylheptyl, 1,1,3-trimethylhexyl or
- R 1 and R 2 as C 5 -C 12 cycloalkyl can be, for example, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl or cyclododecyl. Cyclopentyl and cyclohexyl are preferred, especially cyclohexyl.
- R 1 and R 2 are C 5 -C 6 -cycloalkyl-methyl, this means cyclopentylmethyl and especially cyclohexylmethyl.
- R 1 and R 2 are C 5 -C 6 -cycloalkyl-methyl, this means cyclopentylmethyl and especially cyclohexylmethyl.
- R 1 and R 2 are, for example, decalinylmethyl as C 9 -C 10 bicycloalkylmethyl. As C 9 -C 10 tricycloalkylmethyl, R 1 and R 2 preferably have the meaning of a group of the formula
- alkylphenyl examples include methylphenyl, dimethylphenyl, trimethylphenyl, Ethylphenyl, isopropylphenyl, t-butylphenyl, di-t-butylphenyl or 2,6 di-t-butyl-4-methylphenyl.
- the invention also relates to the use of component B) as additives in Lubricants (industrial oils or greases), hydraulic or metalworking fluids, preferred in hydraulic and gear oils.
- Lubricants industrial oils or greases
- the use according to the invention closes the protection of the metal parts to be lubricated from mechanical Wear (high pressure and wear protection) and an anti-corrosion effect on. Therefore, the present invention also relates to a method for improvement the performance characteristics of lubricants, metalworking and Hydraulic fluids, characterized in that these compounds of Formula I can be added.
- the lubricants or fuels mentioned are based for example on mineral or synthetic oils or mixtures thereof.
- the lubricants are familiar to the specialist and in the relevant specialist literature, as for example in Dieter Klamann, "Lubricants and related Products “(Verlag Chemie, Weinheim, 1982), in Schewe-Kobek,” The Lubricant Paperback “ (Dr. Alfred Wilsonhig-Verlag, Heidelberg, 1974) and in “Ullmanns Encyclopedia of Technical Chemistry ", Vol. 13, pages 85-94 (Verlag Chemie, Weinheim, 1977).
- the lubricants are especially oils and fats, for example based on a mineral oil. Oils are preferred.
- lubricants that can be used are vegetable or animal oils, fats, tallow and waxes or their mixtures with each other or mixtures with the mineral or synthetic oils mentioned.
- Vegetable and animal oils, fats, tallow and waxes are for example Tree nut oil and mixtures thereof, fish oils, tallow from slaughter animals such as Beef tallow, claw fat and bone oil as well as their modified, epoxidized and sulfoxidized forms, for example epoxidized soybean oil.
- the mineral oils are based in particular on hydrocarbon compounds.
- Examples of synthetic lubricants include based lubricants the aliphatic or aromatic carboxyl esters, the polymeric esters, the Polyalkylene oxides, phosphoric acid esters, poly- ⁇ -olefins or silicones, a diester of a dihydric acid with a monohydric alcohol, e.g. Dioctyl sebacate or dinonyl adipate, a triester of trimethylolpropane with a monovalent acid or with a mixture of such acids, e.g.
- Trimethylolpropane tripelargonate Trimethylolpropane tricaprylate or mixtures thereof, one Pentaerythritol tetraesters with a monovalent acid or with a mixture such acids, e.g. Pentaerythritol tetracaprylate, or a complex ester of monohydric and dihydric acids with polyhydric alcohols, e.g. on complex ester of trimethylolpropane with caprylic and sebacic acid or of a mixture of them.
- mineral oils e.g. Poly- ⁇ -olefins, Ester based lubricants, phosphates, glycols, polyglycols and Polyalkylene glycols and their mixtures with water.
- Industrial oils, greases, metalworking fluids and hydraulic fluids can be produced on the basis of the same substances as for the above Lubricant described. Often these are also emulsions such substances in water or other liquids.
- Lubricant compositions according to the invention find e.g. Use in Internal combustion engines, e.g. in motor vehicles, e.g. with motors of the Otto, diesel, two-stroke, Wankel or orbital types.
- Component B is also suitable as an additive for fuels in motor vehicles, which are equipped with motors of the type mentioned.
- the compounds of the formula I are used in lubricants, fuels, metalworking and hydraulic fluids well soluble and therefore as additives Lubricants, metalworking and hydraulic fluids are particularly suitable.
- compositions advantageously contain 0.005 to 1.0% by weight of one Compound of the formula I, preferably 0.005-0.1% by weight, in particular 0.005- 0.05% by weight.
- compositions advantageously contain 0.005 to 1.0% by weight of one Compound of the formula I, preferably 0.005-0.1% by weight, in particular 0.005- 0.05% by weight.
- the compounds of formula I can the lubricants or fuels per se be mixed in a known manner.
- the compounds are in oils, for example readily soluble. It is also possible to produce a so-called master batch that in accordance with the consumption to use concentrations with the corresponding Lubricant can be diluted. In such cases there are also concentrations over 1% by weight possible.
- the lubricants or fuels, metalworking and hydraulic fluids can additionally contain other additives that be added to further improve their basic properties; to include: antioxidants, metal passivators, other rust inhibitors, viscosity index improvers, Pour point depressants, solid lubricants, dispersants, Detergents, anti-foaming agents, other high-pressure additives, anti-wear additives and coefficient of friction.
- additives are used in the usual way Amounts in the range of about 0.01 to 10.0% by weight each.
- viscosity index improvers examples include: polyacrylates, polymethacrylates, vinyl pyrrolidone / methacrylate copolymers, polyvinyl pyrrolidones, polybutenes, olefin copolymers, styrene / acrylate copolymers, polyethers.
- pour point depressants are: polymethacrylate, alkylated naphthalene derivatives.
- dispersants / surfactants are: polybutenylsuccinic acid amides or - imides, polybutenylphosphonic acid derivatives, basic magnesium, calcium and barium sulfonates and phenolates.
- anti-foaming agents silicone oils and polymethacrylene.
- solid lubricants examples include Teflon TM or molybdenum sulfide.
- wear protection additives are: Sulfur and / or phosphorus and / or halogen-containing compounds, such as sulfurized olefins and vegetable oils, zinc dialkyldithiophosphates, tritolyl phosphate, tricresyl phosphate, chlorinated paraffins, alkyl and aryl di- and tri-sulfides, amine salts of mono- and Dialkyl phosphates, amine salts of methylphosphonic acid, diethanolaminomethyltolyltriazole, di (2-ethylhexyl) aminomethyltolyltriazole, derivatives of 2,5-dimercapto-1,3,4-thiadiazole, 3 - [(bis-isopropyloxy-phosphinothioyl) thio] -prophosphate-ethyl-propionate (Triphenylphosphorothioate), tris (alkylphenyl) phosphorothioate and mixtures thereof (
- the compounds according to the invention are prepared, for example, according to the following scheme: CA 90: 120801s] and in LA Belova, et al, Zh. Obshch. Khim 51 (9) (1981) 1982-88 (Russian) [CA 96: 103597 m].
- compositions are good wear protection and especially the very good load carrying properties - especially for hydraulic and Gear oils, with surprisingly relatively small amounts of ⁇ -dithiophosphorylated Sufficient propionic acids. This can cause any negative Accompanying effects such as corrosiveness to Cu and incompatibility with any existing ones Ca compounds (precipitation reactions) can be minimized. Furthermore, a additional corrosion protection potential available.
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Description
Die vorliegende Erfindung betrifft Zusammensetzungen, die einen Schmierstoff (vorzugsweise ein Industrieöl oder ein Fett), eine Metallbearbeitungs- oder eine Hydraulikflüssigkeit und mindestens eine β-dithiophosphorylierte Propionsäure der unten beschriebenen Formel I enthalten.The present invention relates to compositions containing a lubricant (preferably an industrial oil or a grease), a metalworking or a Hydraulic fluid and at least one β-dithiophosphorylated propionic acid Formula I described below.
Modernen Schmierstoffen werden Additive zugesetzt, welche Aufgaben wie Hochdruck- und Verschleißschutz, Korrosionschutz und Antioxidationswirkung erfüllen [W. J. Bartz (Editor), et al., "Additive für Schmierstoffe" (expert-Verlag 1994)]. Eine besondere Bedeutung kommt dabei den Zinkdialkyldithiophosphaten zu, die antioxidative und Hochdruck- und Verschleißschutzwirkung in sich vereinigen. In neuerer Zeit ist man bemüht, diese schwermetallhaltigen Zusatzstoffe weitgehend durch metallfreie Verbindungen zu ersetzen, weil dies umweltfreundlich ist und sich positiv auf die Lebensdauer der Abgas-Katalysatoren von Verbrennungsmotoren auswirkt. Es besteht in der Industrie zur Zeit ein Bedürfnis an metallfreien und aschefreien Additiven. Ester des Typs: sind unter dem Handelsnamen lrgalube™ 63 erhältlich. Ferner sind in US 4,333,841 dithiophosphorylierte Mercaptoessigsäuren und deren Salze als Schmierstoffzusätze beschrieben.Additives are added to modern lubricants, which perform tasks such as high-pressure and wear protection, corrosion protection and antioxidation effects [WJ Bartz (Editor), et al., "Additives for lubricants" (expert-Verlag 1994)]. Zinc dialkyldithiophosphates, which combine antioxidative and high-pressure and wear protection effects, are of particular importance. In recent times, efforts have been made to largely replace these heavy metal additives with metal-free compounds, because this is environmentally friendly and has a positive effect on the service life of the exhaust gas catalysts of internal combustion engines. There is currently a need in the industry for metal-free and ash-free additives. Type of ester: are available under the trade name lrgalube ™ 63. Furthermore, US 4,333,841 dithiophosphorylated mercaptoacetic acids and their salts are described as lubricant additives.
Bis-Dithiophosphorsäurederivate werden in GB-A 2'267'493 als Schmiermitteladditive beschrieben. Für dieselbe Anwendung werden in EP-A 98,809 [CA 101: 55323 s] Salze der Formel (RO)2P(S)S (CH2)n (C(O)OM, M = Li, K, Na, HNR, vorgeschlagen. US-A 5,362,419 beschreibt als Zwischenprodukte Säuren der Formel (RO)2P(S)S (CH2)2 C(O)OH zur Herstellung von als Schmierstoffzusätze geeigneten Glykolestern, wie z.B. (RO)2P(S)(CH2)2 C(O)OCH2 (CHOH)CH2OH (s. auch H. Zinke, R. Schumacher, Wear 179 (1-2) (1994) 45-8 [CA 122: 85158 t]).Bis-dithiophosphoric acid derivatives are described in GB-A 2'267'493 as lubricant additives. For the same application, EP-A 98,809 [CA 101: 55323 s] salts of the formula (RO) 2 P (S) S (CH 2 ) n (C (O) OM, M = Li, K, Na, HNR, US-A 5,362,419 describes as intermediates acids of the formula (RO) 2 P (S) S (CH 2 ) 2 C (O) OH for the production of glycol esters suitable as lubricant additives, such as (RO) 2 P (S) ( CH 2 ) 2 C (O) OCH 2 (CHOH) CH 2 OH (see also H. Zinke, R. Schumacher, Wear 179 (1-2) (1994) 45-8 [CA 122: 85158 t]).
Es wurde überraschenderweise gefunden, daß die den oben angeführten Propionsäureeestern zugrundeliegenden β-dithiophosphorylierten Propionsäuren selbst schon bei sehr kleinen Konzentrationen hervorragende Hochdruck- und Verschleißschutzmittel darstellen. It has surprisingly been found that the above-mentioned propionic acid esters underlying β-dithiophosphorylated propionic acids themselves excellent high-pressure and wear protection agents even at very low concentrations represent.
Die Erfindung betrifft daher Zusammensetzungen (vorzugsweise zink- und aschefrei)
enthaltend
Bevorzugt sind bei der Komponente B) R1 und R2 unabhängig voneinander C3-C18-Alkyl, C5-C6-Cycloalkyl oder C7-C18-Alkylphenyl.In component B), R 1 and R 2 are, independently of one another, C 3 -C 18 alkyl, C 5 -C 6 cycloalkyl or C 7 -C 18 alkylphenyl.
Besonders bevorzugt sind bei der Komponente B) R1 und R2 i-Propyl, i-Butyl oder 2-Ethyl-hexyl, und R3 Wasserstoff.Component B) R 1 and R 2 are particularly preferably i-propyl, i-butyl or 2-ethylhexyl, and R 3 is hydrogen.
Stellen in der obigen Formel I R1 und R2 C3-C18-Alkyl dar, so handelt es sich dabei um verzweigte oder unverzweigte Reste. Beispiele hierfür sind Propyl, Isopropyl, n-Butyl, Isobutyl, t-Butyl, Pentyl, Isopentyl, Hexyl, Heptyl, 3-Heptyl, Octyl, 2-Ethylhexyl, Nonyl, Decyl, Undecyl, Dodecyl, Tridecyl, Tetradecyl, Pentadecyl, Hexadecyl, Heptadecyl, Octadecyl, 2-Ethylbutyl, 1-Methylpentyl, 1,3-Dimethylbutyl, 1,1,3,3-Tetramethylbutyl, 1-Methylhexyl, Isoheptyl, 1-Methylheptyl, 1,1,3-Trimethylhexyl oder 1-Methylundecyl.If IR 1 and R 2 are C 3 -C 18 -alkyl in the above formula, these are branched or unbranched radicals. Examples include propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, isopentyl, hexyl, heptyl, 3-heptyl, octyl, 2-ethylhexyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl , Heptadecyl, octadecyl, 2-ethylbutyl, 1-methylpentyl, 1,3-dimethylbutyl, 1,1,3,3-tetramethylbutyl, 1-methylhexyl, isoheptyl, 1-methylheptyl, 1,1,3-trimethylhexyl or 1-methylundecyl .
R1 und R2 als C5-C12-Cycloalkyl können z.B. Cyclopentyl, Cyclohexyl, Cycloheptyl, Cyclooctyl oder Cyclododecyl sein. Cyclopentyl und Cyclohexyl sind bevorzugt, insbesondere Cyclohexyl.R 1 and R 2 as C 5 -C 12 cycloalkyl can be, for example, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl or cyclododecyl. Cyclopentyl and cyclohexyl are preferred, especially cyclohexyl.
Sind R1 und R2 C5-C6-Cycloalkyl-methyl, so ist darunter Cyclopentylmethyl und vor allem Cyclohexylmethyl zu verstehen. If R 1 and R 2 are C 5 -C 6 -cycloalkyl-methyl, this means cyclopentylmethyl and especially cyclohexylmethyl.
Sind R1 und R2 C5-C6-Cycloalkyl-methyl, so ist darunter Cyclopentylmethyl und vor allem Cyclohexylmethyl zu verstehen.If R 1 and R 2 are C 5 -C 6 -cycloalkyl-methyl, this means cyclopentylmethyl and especially cyclohexylmethyl.
Als C9-C10-Bicycloalkyl-methyl sind R1 und R2 z.B. Decalinylmethyl. Als C9-C10-Tricycloalkyl-methyl haben R1 und R2 vorzugsweise die Bedeutung einer Gruppe der Formel R 1 and R 2 are, for example, decalinylmethyl as C 9 -C 10 bicycloalkylmethyl. As C 9 -C 10 tricycloalkylmethyl, R 1 and R 2 preferably have the meaning of a group of the formula
Beispiele für Alkylphenyl sind Methylphenyl, Dimethylphenyl, Trimethylphenyl, Ethylphenyl, Isopropylphenyl, t-Butylphenyl, Di-t-butylphenyl oder 2,6 Di-t-butyl-4-methylphenyl.Examples of alkylphenyl are methylphenyl, dimethylphenyl, trimethylphenyl, Ethylphenyl, isopropylphenyl, t-butylphenyl, di-t-butylphenyl or 2,6 di-t-butyl-4-methylphenyl.
Die Erfindung betrifft auch die Verwendung der Komponente B) als Additive in Schmierstoffen (Industrieölen oder Fetten), Hydraulik- oder Metallbearbeitungsflüssigkeiten, bevorzugt in Hydraulik- und Getriebeölen. Die erfindungsgemäße Verwendung schließt den Schutz der zu schmierenden Metallteile vor mechanischer Abnutzung (Hochdruck- und Verschleißschutz) sowie eine Korrosionsschutzwirkung ein. Daher betrifft die vorliegende Erfindung ebenfalls ein Verfahren zur Verbesserung der Gebrauchseigenschaften von Schmierstoffen, Metallbearbeitungs- und Hydraulikflüssigkeiten, dadurch gekennzeichnet, daß diesen Verbindungen der Formel I zugesetzt werden.The invention also relates to the use of component B) as additives in Lubricants (industrial oils or greases), hydraulic or metalworking fluids, preferred in hydraulic and gear oils. The use according to the invention closes the protection of the metal parts to be lubricated from mechanical Wear (high pressure and wear protection) and an anti-corrosion effect on. Therefore, the present invention also relates to a method for improvement the performance characteristics of lubricants, metalworking and Hydraulic fluids, characterized in that these compounds of Formula I can be added.
Die erwähnten Schmier- oder Kraftstoffe (wie z.B. Industrieöle und Fette), Metallbearbeitungs- und Hydraulikflüssigkeiten der Komponente A) basieren beispielsweise auf mineralischen oder synthetischen Ölen oder Mischungen davon. Die Schmierstoffe sind dem Fachmann geläufig und in der einschlägigen Fachliteratur, wie beispielsweise in Dieter Klamann, "Schmierstoffe und verwandte Produkte" (Verlag Chemie, Weinheim, 1982), in Schewe-Kobek, "Das Schmiermittel-Taschenbuch" (Dr. Alfred Hüthig-Verlag, Heidelberg, 1974) und in "Ullmanns Enzyklopädie der technischen Chemie", Bd.13, Seiten 85-94 (Verlag Chemie, Weinheim, 1977) beschrieben.The lubricants or fuels mentioned (such as industrial oils and greases), Metalworking and hydraulic fluids of component A) are based for example on mineral or synthetic oils or mixtures thereof. The lubricants are familiar to the specialist and in the relevant specialist literature, as for example in Dieter Klamann, "Lubricants and related Products "(Verlag Chemie, Weinheim, 1982), in Schewe-Kobek," The Lubricant Paperback " (Dr. Alfred Hüthig-Verlag, Heidelberg, 1974) and in "Ullmanns Encyclopedia of Technical Chemistry ", Vol. 13, pages 85-94 (Verlag Chemie, Weinheim, 1977).
Die Schmierstoffe sind insbesondere Öle und Fette, beispielsweise basierend auf einem Mineralöl. Bevorzugt sind Öle.The lubricants are especially oils and fats, for example based on a mineral oil. Oils are preferred.
Eine weitere Gruppe von Schmierstoffen, die zur Anwendung gelangen können, sind pflanzliche oder tierische Öle, Fette, Talge und Wachse oder deren Gemische untereinander oder Gemische mit den erwähnten mineralischen oder synthetischen Ölen. Pflanzliche und tierische Öle, Fette, Talge und Wachse sind beispielsweise Baumnußöl und Mischungen davon, Fischöle, Talge von Schlachttieren wie Rindertalg, Klauenfett und Knochenöl sowie deren modifizierte, epoxidierte und sulfoxidierte Formen, beispielsweise epoxidiertes Sojabohnenöl. Die Mineralöle basieren insbesondere auf Kohlenwasserstoffverbindungen.Another group of lubricants that can be used are vegetable or animal oils, fats, tallow and waxes or their mixtures with each other or mixtures with the mineral or synthetic oils mentioned. Vegetable and animal oils, fats, tallow and waxes are for example Tree nut oil and mixtures thereof, fish oils, tallow from slaughter animals such as Beef tallow, claw fat and bone oil as well as their modified, epoxidized and sulfoxidized forms, for example epoxidized soybean oil. The mineral oils are based in particular on hydrocarbon compounds.
Beispiele von synthetischen Schmierstoffen umfassen Schmierstoffe auf der Basis der aliphatischen oder aromatischen Carboxylester, der polymeren Ester, der Polyalkylenoxide, der Phosphorsäureester, der Poly-α-olefine oder der Silicone, eines Diesters einer zweiwertigen Säure mit einem einwertigen Alkohol, wie z.B. Dioctylsebacat oder Dinonyladipat, eines Triesters von Trimethylolpropan mit einer einwertigen Säure oder mit einem Gemisch solcher Säuren, wie z.B. Trimethylolpropantripelargonat, Trimethylolpropan-tricaprylat oder Gemische davon, eines Tetraesters von Pentaerythrit mit einer einwertigen Säure oder mit einem Gemisch solcher Säuren, wie z.B. Pentaerythrit-tetracaprylat, oder eines komplexen Esters von einwertigen und zweiwertigen Säuren mit mehrwertigen Alkoholen, z.B. ein komplexer Ester von Trimethylolpropan mit Capryl- und Sebacinsäure oder von einem Gemisch davon. Besonders geeignet sind neben Mineralölen z.B. Poly-α-Olefine, Schmierstoffe auf Esterbasis, Phosphate, Glykole, Polyglykole und Polyalkylenglykole, sowie deren Mischungen mit Wasser.Examples of synthetic lubricants include based lubricants the aliphatic or aromatic carboxyl esters, the polymeric esters, the Polyalkylene oxides, phosphoric acid esters, poly-α-olefins or silicones, a diester of a dihydric acid with a monohydric alcohol, e.g. Dioctyl sebacate or dinonyl adipate, a triester of trimethylolpropane with a monovalent acid or with a mixture of such acids, e.g. Trimethylolpropane tripelargonate, Trimethylolpropane tricaprylate or mixtures thereof, one Pentaerythritol tetraesters with a monovalent acid or with a mixture such acids, e.g. Pentaerythritol tetracaprylate, or a complex ester of monohydric and dihydric acids with polyhydric alcohols, e.g. on complex ester of trimethylolpropane with caprylic and sebacic acid or of a mixture of them. In addition to mineral oils, e.g. Poly-α-olefins, Ester based lubricants, phosphates, glycols, polyglycols and Polyalkylene glycols and their mixtures with water.
Industrieöle, Fette, Metallbearbeitungsflüssigkeiten und Hydraulikflüssigkeiten können auf Basis der gleichen Substanzen hergestellt werden wie vorstehend für die Schmiermittel beschrieben. Häufig handelt es sich dabei auch um Emulsionen solcher Substanzen in Wasser oder anderen Flüssigkeiten.Industrial oils, greases, metalworking fluids and hydraulic fluids can be produced on the basis of the same substances as for the above Lubricant described. Often these are also emulsions such substances in water or other liquids.
Erfindungsgemäße Schmierstoffzusammensetzungen finden z.B. Verwendung in Verbrennungsmotoren, z.B. in Kraftfahrzeugen, ausgerüstet z.B. mit Motoren des Otto-, Diesel-, Zweitakt-, Wankel- oder Orbitaltyps.Lubricant compositions according to the invention find e.g. Use in Internal combustion engines, e.g. in motor vehicles, e.g. with motors of the Otto, diesel, two-stroke, Wankel or orbital types.
Die Komponente B ist auch als Additiv für Kraftstoffe in Kraftfahrzeugen geeignet, welche mit den Motoren des genannten Typs ausgerüstet sind.Component B is also suitable as an additive for fuels in motor vehicles, which are equipped with motors of the type mentioned.
Die Verbindungen der Formel I sind in Schmierstoffen, Kraftstoffen, Metallbearbeitungs- und Hydraulikflüssigkeiten gut löslich und deshalb als Zusätze zu Schmierstoffen, Metallbearbeitungs- und Hydraulikflüssigkeiten besonders geeignet.The compounds of the formula I are used in lubricants, fuels, metalworking and hydraulic fluids well soluble and therefore as additives Lubricants, metalworking and hydraulic fluids are particularly suitable.
Vorteilhafterweise enthalten die Zusammensetzungen 0,005 bis zu 1,0 Gew.% einer Verbindung der Formel I, bevorzugt 0,005 - 0,1 Gew.%, insbesondere 0,005 - 0,05 Gew. %. The compositions advantageously contain 0.005 to 1.0% by weight of one Compound of the formula I, preferably 0.005-0.1% by weight, in particular 0.005- 0.05% by weight.
Vorteilhafterweise enthalten die Zusammensetzungen 0,005 bis zu 1,0 Gew.% einer Verbindung der Formel I, bevorzugt 0,005 - 0,1 Gew.%, insbesondere 0,005 - 0,05 Gew. %.The compositions advantageously contain 0.005 to 1.0% by weight of one Compound of the formula I, preferably 0.005-0.1% by weight, in particular 0.005- 0.05% by weight.
Die Verbindungen der Formel I können den Schmier- oder Kraftstoffen auf an sich bekannte Weise beigemischt werden. Die Verbindungen sind beispielsweise in Ölen gut löslich. Es ist auch möglich, einen sogenannten Masterbatch herzustellen, der nach Maßgabe des Verbrauchs auf Einsatzkonzentrationen mit dem entsprechenden Schmierstoff verdünnt werden kann. In solchen Fällen sind auch Konzentrationen über 1 Gew.% möglich.The compounds of formula I can the lubricants or fuels per se be mixed in a known manner. The compounds are in oils, for example readily soluble. It is also possible to produce a so-called master batch that in accordance with the consumption to use concentrations with the corresponding Lubricant can be diluted. In such cases there are also concentrations over 1% by weight possible.
Die erfindungsgemäß stabilisierten Schmier- oder Kraftstoffe, Metallbearbeitungs- und Hydraulikflüssigkeiten können zusätzlich andere Additive enthalten, die zugegeben werden, um ihre Grundeigenschaften noch weiter zu verbessern; dazu gehören: Antioxidantien, Metallpassivatoren, weitere Rostinhibitoren, Viskositätsindex-Verbesserer, Stockpunkterniedriger, Festschmierstoffe, Dispergiermittel, Detergentien, Antischaummittel, weitere Hochdruck-Zusätze, Antiverschleiß-Additive und Reibwertverminderer. Solche Additive gibt man in den jeweils dafür üblichen Mengen im Bereich von je etwa 0,01 bis 10,0 Gew.% zu.The lubricants or fuels, metalworking and hydraulic fluids can additionally contain other additives that be added to further improve their basic properties; to include: antioxidants, metal passivators, other rust inhibitors, viscosity index improvers, Pour point depressants, solid lubricants, dispersants, Detergents, anti-foaming agents, other high-pressure additives, anti-wear additives and coefficient of friction. Such additives are used in the usual way Amounts in the range of about 0.01 to 10.0% by weight each.
Es folgen Beispiele solcher weiteren Zusatzstoffe:The following are examples of such other additives:
Beispiele für phenolische Antioxidantien:
Aliphatische oder aromatische Phosphite, Ester der Thiodipropionsäure oder der Thiodiessigsäure, oder Salze der Dithiocarbamid- oder Dithiophosphorsäure, 2,2,12,12-Tetramethyl-5,9-dihydroxy-3,7,11-trithiatridecan und 2,2,15,15-Tetramethyl-5,12-dihydroxy-3,7,10,14-tetrathiahexadecan.Aliphatic or aromatic phosphites, esters of thiodipropionic acid or Thiodiacetic acid, or salts of dithiocarbamide or dithiophosphoric acid, 2,2,12,12-tetramethyl-5,9-dihydroxy-3,7,11-trithiatridecane and 2,2,15,15-tetramethyl-5,12-dihydroxy-3,7,10,14-tetrathiahexadecane.
Beispiele für Metall-Desaktivatoren, z.B. für Kupfer, sind:
Beispiele für Rost-Inhibitoren sind:
Beispiele für Viskositätsindex-Verbesserer sind: Polyacrylate, Polymethacrylate, Vinylpyrrolidon/Methacrylat-Copolymere, Polyvinylpyrrolidone, Polybutene, Olefin-Copolymere, Styrol/Acrylat-Copolymere, Polyether. Examples of viscosity index improvers are: polyacrylates, polymethacrylates, vinyl pyrrolidone / methacrylate copolymers, polyvinyl pyrrolidones, polybutenes, olefin copolymers, styrene / acrylate copolymers, polyethers.
Beispiele für Stockpunkterniedriger sind: Polymethacrylat, alkylierte Naphthalinderivate. Examples of pour point depressants are: polymethacrylate, alkylated naphthalene derivatives.
Beispiele für Dispergiermittel/Tenside sind: Polybutenylbernsteinsäureamide oder - imide, Polybutenylphosphonsäurederivate, basische Magnesium-, Calcium-, und Bariumsulfonate und -phenolate. Examples of dispersants / surfactants are: polybutenylsuccinic acid amides or - imides, polybutenylphosphonic acid derivatives, basic magnesium, calcium and barium sulfonates and phenolates.
Beispiele für Antischaummittel sind: Silikonöle und Polymethacrylen. Examples of anti-foaming agents are: silicone oils and polymethacrylene.
Beispiele für Festschmierstoffe sind: Teflon™ oder Molybdänsulfid. Examples of solid lubricants are: Teflon ™ or molybdenum sulfide.
Beispiele für Verschleißschutz-Additive sind: Schwefel und/oder Phosphor und/oder Halogen enthaltende Verbindungen, wie geschwefelte Olefine und pflanzliche Oele, Zinkdialkyldithiophosphate, Tritolylphosphat, Tricresylphosphat, chlorierte Paraffine, Alkyl- und Aryldi- und tri-sulfide, Aminsalze von Mono- und Dialkylphosphaten, Aminsalze der Methylphosphonsäure, Diethanolaminomethyltolyltriazol, Di(2-ethylhexyl)aminomethyltolyltriazol, Derivate des 2,5-Dimercapto-1,3,4-thiadiazols, 3-[(Bis-isopropyloxy-phosphinothioyl)thio]-propionsäure-ethylester, Triphenylthiophosphat (Triphenylphosphorothioat), Tris(alkylphenyl)phosphorothioate und deren Gemische, (z.B. Tris(isononylphenyl)phosphorothioat), Diphenyl-monononylphenyl-phosphorothioat, Isobutylphenyl-diphenyl-phosphorothioat, Dodecylaminsalz des 3-Hydroxy-1,3-thiaphosphetan-3-oxids, Trithiophosphorsäure-5,5,5-tris[isooctylacetat (2)], Derivate von 2-Mercaptobenzthiazol wie 1-[N,N-Bis(2-ethylhexyl)aminomethyl]-2-mercapto-1H-1,3-benzthiazol, Ethoxycarbonyl-5-octyldithiocarbamat. Examples of wear protection additives are: Sulfur and / or phosphorus and / or halogen-containing compounds, such as sulfurized olefins and vegetable oils, zinc dialkyldithiophosphates, tritolyl phosphate, tricresyl phosphate, chlorinated paraffins, alkyl and aryl di- and tri-sulfides, amine salts of mono- and Dialkyl phosphates, amine salts of methylphosphonic acid, diethanolaminomethyltolyltriazole, di (2-ethylhexyl) aminomethyltolyltriazole, derivatives of 2,5-dimercapto-1,3,4-thiadiazole, 3 - [(bis-isopropyloxy-phosphinothioyl) thio] -prophosphate-ethyl-propionate (Triphenylphosphorothioate), tris (alkylphenyl) phosphorothioate and mixtures thereof (e.g. tris (isononylphenyl) phosphorothioate), diphenyl monononylphenyl phosphorothioate, isobutylphenyl diphenyl phosphorothioate, dodecylamine salt of 3-hydroxy-1,3-thiaphosphetane Trithiophosphoric acid 5,5,5-tris [isooctylacetate (2)], derivatives of 2-mercaptobenzothiazole such as 1- [N, N-bis (2-ethylhexyl) aminomethyl] -2-mercapto-1H-1,3-benzthi azole, ethoxycarbonyl-5-octyldithiocarbamate.
Die Verbindungen der Formel I und ihre Herstellung sind an sich bekannt. Sie dienen in erster Linie als Zwischenprodukte für diverse Produkte und Anwendungen, wie z.B in V.V. Ovchinnikov, et al., Org. React (Tartu) 15(2) (1978), 194-203 (engl.) [CA 90: 120801s] sowie in L.A. Belova, et al, Zh. Obshch. Khim 51 (9) (1981) 1982-88 (russ.) [CA 96: 103597 m], beschrieben.The compounds of formula I and their preparation are known per se. she primarily serve as intermediates for various products and applications, as e.g. in V.V. Ovchinnikov, et al., Org. React (Tartu) 15 (2) (1978), 194-203 [CA 90: 120801s] and in L.A. Belova, et al, Zh. Obshch. Khim 51 (9) (1981) 1982-88 (Russian) [CA 96: 103597 m].
Die Herstellung der erfindungsgemäßen Verbindungen erfolgt beispielsweise nach
dem folgenden Schema:
CA 90: 120801s] sowie in L.A. Belova, et al, Zh. Obshch. Khim 51 (9) (1981) 1982-88
(russ.) [CA 96: 103597 m], beschrieben.The compounds according to the invention are prepared, for example, according to the following scheme:
CA 90: 120801s] and in LA Belova, et al, Zh. Obshch. Khim 51 (9) (1981) 1982-88 (Russian) [CA 96: 103597 m].
Die Herstellung der erfindungsgemäßen Verbindungen erfolgt beispielsweise nach dem folgenden Schema: The compounds according to the invention are prepared, for example, according to the following scheme:
Diese Synthese von β-dithiophosphorylierter Propionsäure durch Addition von Dithiophosphorsäure an Acryl- oder Methacrylsäure ist bekannt und beispielsweise in US 5,362,419 (Bsp. 1-11) beschrieben. Die folgenden Beispiele 1-3 dokumentieren die Synthese einiger in den erfindungsgemäßen Zusammensetzungen verwandten b-dithiophosphorylierten Propionsäuren. Teile- und Prozentangaben beziehen sich, sofern nicht anders angegeben, auf das Gewicht. This synthesis of β-dithiophosphorylated propionic acid by adding dithiophosphoric acid to acrylic or methacrylic acid is known and is described, for example, in US Pat. No. 5,362,419 (Ex. 1-11). The following examples 1-3 document the synthesis of some b-dithiophosphorylated propionic acids used in the compositions according to the invention. Unless otherwise stated, parts and percentages are by weight.
Zu 21,4 g (0.1 mol) O,O-Diisopropyldithiophosphorsäure in 50 ml Toluol werden
innerhalb von 20 min. bei 80°C 7,2 g (0.1 mol) Acrylsäure zugetropft. Es wird 5 h
bei 80°C weitergerührt. Nach Abziehen des Lösungsmittels am Rotationsverdampfer
wird der Rückstand säulenchromatographisch an Silicagel fraktioniert: Man erhält
11,8 g gelbes, flüssiges Hauptprodukt (41 % d. Th.).
Zu 252,4 g (0.1 mol) O,O-Diisobutyldithiophosphorsäure werden bei 70°C innerhalb
von 1 h 81,4 g (1.1 mol) Acrylsäure zugetropft, und es wird 4 h bei 70°C weitergerührt.
Das Rohprodukt wird in 500 ml Natriumhydroxid 2N gelöst und mit zweimal
300 ml Siedegrenzbenzin (Sdp. 80-110°C) gewaschen. Dann wird mit konz.
Salzsäure auf pH 1 angesäuert und mit ca. 150 ml Siedegrenzbenzin extrahiert. Die
organische Phase wird mit Wasser gewaschen und am Rotationsverdampfer
eingedampft: Es ergeben sich 287,6 g klares, mittelviskoses, hellgelbes Öl(91 % d.
Th.).
1H-NMR (in CDCl3-Lösung, relativ zu Tetramethylsilan):81.4 g (1.1 mol) of acrylic acid are added dropwise at 70 ° C. to 252.4 g (0.1 mol) of O, O-diisobutyldithiophosphoric acid, and stirring is continued at 70 ° C. for 4 h. The crude product is dissolved in 500 ml of 2N sodium hydroxide and washed twice with 300 ml of mineral spirits (bp 80-110 ° C). Then with conc. Acidified hydrochloric acid to pH 1 and extracted with approx. 150 ml of mineral spirits. The organic phase is washed with water and evaporated on a rotary evaporator: 287.6 g of clear, medium-viscosity, light yellow oil (91% of theory) result.
1 H-NMR (in CDCl 3 solution, relative to tetramethylsilane):
1.02 ppm (d, 12H), 2.05 ppm (hept, 2H), 2,86 ppm (t, 2H), 3.17 ppm (d x t, 2H), 3.89 ppm (d x hept, 4H). 1.02 ppm (d, 12H), 2.05 ppm (hept, 2H), 2.86 ppm (t, 2H), 3.17 ppm (dxt, 2H), 3.89 ppm (dx hept, 4H).
Zu 35,5 g (0.1 mol) O,O-Di(2-ethylhexyl)dithiophosphorsäure in 50 ml Toluol werden
bei 75°C innerhalb von 15 min. 7,21 g (1.1 mol) Acrylsäure zugetropft. Es wird 5 h
bei 75°C weitergerührt. Die Aufarbeitung erfolgt wie in Bsp. 1, und man erhält 21,8 g
gelbliches Öl (51 % d. Th.).
Die Vorteile der Zusammensetzungen liegen im guten Verschleißschutz und besonders den sehr guten Lasttrage-Eigenschaften - speziell für Hydraulik- und Getriebeöle, wobei überraschenderweise relativ geringe Mengen an β-dithiophosphorylierten Propionsäuren ausreichen. Dadurch können eventuelle negative Begleiteffekte wie Korrosivität gegenüber Cu und Unverträglichkeit mit etwa vorhandenen Ca-Verbindungen (Fällungsreaktionen) minimiert werden. Ferner ist ein zusätzliches Korrosionschutzpotential vorhanden.The advantages of the compositions are good wear protection and especially the very good load carrying properties - especially for hydraulic and Gear oils, with surprisingly relatively small amounts of β-dithiophosphorylated Sufficient propionic acids. This can cause any negative Accompanying effects such as corrosiveness to Cu and incompatibility with any existing ones Ca compounds (precipitation reactions) can be minimized. Furthermore, a additional corrosion protection potential available.
Für Hydraulik- und Getriebeöle sind sowohl ein sehr guter Verschleißschutz (antiwear, AW) als auch ein sehr gutes Lasttragevermögen (extreme pressure, EP) gefordert. For hydraulic and gear oils, both very good wear protection (antiwear, AW) as well as a very good load bearing capacity (extreme pressure, EP) required.
Ausgezeichnete Werte im FZG-Test (Fehlerlaststufe > 12) sind mit den üblichen Verschleißschutzadditiven bei niedrigen Einsatzkonzentrationen (geringer als 0.2%) nur schwer zu erreichen. Überraschenderweise erzielt man jedoch mit relativ geringen Konzentrationen an Verbindungen der Formel I (bereits 0.005-0.05%) sehr gute bis ausgezeichnete FZG-Werte (vgl Tabelle 1, achte und zehnte Spalte).Excellent values in the FZG test (error load level> 12) are with the usual Wear protection additives at low application concentrations (less than 0.2%) difficult to reach. Surprisingly, however, you can achieve with relatively low Concentrations of compounds of formula I (already 0.005-0.05%) very much good to excellent FZG values (see Table 1, eighth and tenth columns).
Folgende nachstehende Formulierungen wurden im FZG-Getriebetest (Beschreibung in DIN 51.354, A/8.3./90) getestet (Tabelle 1). In diesem Test wird das Lasttragevermögen von Schmiermitteln für die Anwendung als Getriebeöle beurteilt. Im Tauchschmierungsverfahren laufen in dem zu prüfenden Schmieröl definierte Zahnräder bei konstanter Drehzahl und festgelegter Anfangsöltemperatur. Die Belastung der Zahnräder wird stufenweise gesteigert. Ab Kraftstufe 4 wird nach jeder Kraftstufe die Veränderung der Zahnflanken durch Beschreibung und gegebenenfalls durch Photo, Rauheitsmessung oder Kontrastabdruck festgehalten. Die Grenzlaststufe liegt eine Stufe unter der sog. Fehlerlaststufe, bei der die Flanken mindestens zweier Zahnräder eindeutige Schäden (Risse oder ähnliches) aufweisen. The following formulations were tested in the FZG gearbox test (description in DIN 51.354, A / 8.3. / 90) (Table 1). In this test, the load carrying capacity of lubricants for use as gear oils is assessed. In the splash lubrication process, defined gears run in the lubricating oil to be tested at a constant speed and a specified initial oil temperature. The load on the gears is gradually increased. From force level 4, the change of the tooth flanks is recorded after each force level by description and, if necessary, by photo, roughness measurement or contrast impression. The limit load level is one level below the so-called error load level, at which the flanks of at least two gear wheels have clear damage (cracks or the like).
Claims (13)
- A composition comprisingA) a lubricant or fuel, a metalworking fluid or a hydraulic fluid;B) at least one compound of the formula in whichR1 and R2 independently of one another are C3-C18alkyl, C5-C12cycloalkyl, C5-C6cycloalkylmethyl, C9-C10bicycloalkylmethyl, C9-C10tricycloalkylmethyl, phenyl or C7-C24alkylphenyl or together are (CH3)2C(CH2)2, andR3 is hydrogen or methyl, and, if desired,C) other customary oil additives.
- A composition according to claim 1 containing from 0.005 to 0.01 % by weight of a compound of the formula I.
- A composition according to claim 1 containing 0.005 - 0.05 % by weight of a compound of the formula I.
- A composition according to claim 1, in which component A) is an industrial oil or a grease.
- A composition according to claim 1, in which component A) is a base oil from the group consisting of mineral, vegetable and synthetic oils.
- A composition according to claim 1, in which R1 and R2 independently of one another are C3-C18alkyl, C5-C6cycloalkyl or C7-C18alkylphenyl.
- A composition according to claim 1, in which R1 and R2 are i-propyl, i-butyl or 2-ethylhexyl, and R3 is hydrogen.
- A composition according to claim 1, which additionally comprises C) other oil additives from the groups consisting of antioxidants, metal passivators, rust inhibitors, dispersants, detergents, antifoams, solid lubricants, viscosity index improvers, pour point depressants and antiwear additives.
- A method of improving the service properties of lubricants, hydraulic fluids or metalworking fluids, which comprises adding thereto at least one compound of the formula I as described in claim 1.
- A method according to claim 9 for improving the service properties of hydraulic fluids or transmission oils.
- A zinc-free composition according to claim 1.
- An essentially ash-free composition according to claim 1.
- The use of component B) described in claim 1 as an additive for lubricants, hydraulic fluids or metalworking fluids.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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CH1769/96 | 1996-07-15 | ||
CH176996 | 1996-07-15 | ||
CH176996 | 1996-07-15 |
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Publication Number | Publication Date |
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EP0819754A1 EP0819754A1 (en) | 1998-01-21 |
EP0819754B1 true EP0819754B1 (en) | 2001-04-25 |
Family
ID=4218165
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EP97810446A Expired - Lifetime EP0819754B1 (en) | 1996-07-15 | 1997-07-07 | Beta-dithiophosphorilated propionic acid in lubricants |
Country Status (11)
Country | Link |
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US (1) | US5922657A (en) |
EP (1) | EP0819754B1 (en) |
JP (1) | JP3882154B2 (en) |
KR (1) | KR100441550B1 (en) |
BR (1) | BR9703974A (en) |
CA (1) | CA2210216C (en) |
DE (1) | DE59703420D1 (en) |
ES (1) | ES2157549T3 (en) |
SG (1) | SG84506A1 (en) |
SK (1) | SK283148B6 (en) |
ZA (1) | ZA976208B (en) |
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-
1997
- 1997-07-07 EP EP97810446A patent/EP0819754B1/en not_active Expired - Lifetime
- 1997-07-07 ES ES97810446T patent/ES2157549T3/en not_active Expired - Lifetime
- 1997-07-07 SG SG9702390A patent/SG84506A1/en unknown
- 1997-07-07 DE DE59703420T patent/DE59703420D1/en not_active Expired - Lifetime
- 1997-07-11 KR KR1019970032255A patent/KR100441550B1/en not_active IP Right Cessation
- 1997-07-11 SK SK949-97A patent/SK283148B6/en not_active IP Right Cessation
- 1997-07-11 CA CA002210216A patent/CA2210216C/en not_active Expired - Fee Related
- 1997-07-14 ZA ZA9706208A patent/ZA976208B/en unknown
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US5922657A (en) | 1999-07-13 |
JPH1067993A (en) | 1998-03-10 |
BR9703974A (en) | 1998-11-17 |
ZA976208B (en) | 1998-01-15 |
JP3882154B2 (en) | 2007-02-14 |
MX9705300A (en) | 1998-08-30 |
ES2157549T3 (en) | 2001-08-16 |
KR980009432A (en) | 1998-04-30 |
EP0819754A1 (en) | 1998-01-21 |
CA2210216C (en) | 2006-01-31 |
SG84506A1 (en) | 2001-11-20 |
DE59703420D1 (en) | 2001-05-31 |
CA2210216A1 (en) | 1998-01-15 |
KR100441550B1 (en) | 2004-11-20 |
SK283148B6 (en) | 2003-03-04 |
SK94997A3 (en) | 1998-02-04 |
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