DE69703226T2 - Schmierölzusammensetzung - Google Patents
SchmierölzusammensetzungInfo
- Publication number
- DE69703226T2 DE69703226T2 DE69703226T DE69703226T DE69703226T2 DE 69703226 T2 DE69703226 T2 DE 69703226T2 DE 69703226 T DE69703226 T DE 69703226T DE 69703226 T DE69703226 T DE 69703226T DE 69703226 T2 DE69703226 T2 DE 69703226T2
- Authority
- DE
- Germany
- Prior art keywords
- compound
- lubricating oil
- ppm
- proportion
- groups
- 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 - Fee Related
Links
- 239000010687 lubricating oil Substances 0.000 title claims description 58
- 239000000203 mixture Substances 0.000 title claims description 43
- 150000001875 compounds Chemical class 0.000 claims description 70
- 229910052717 sulfur Inorganic materials 0.000 claims description 18
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 17
- 239000002199 base oil Substances 0.000 claims description 16
- 239000011593 sulfur Substances 0.000 claims description 16
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 13
- 125000003118 aryl group Chemical group 0.000 claims description 13
- 229910052750 molybdenum Inorganic materials 0.000 claims description 13
- 239000011733 molybdenum Substances 0.000 claims description 13
- 230000001050 lubricating effect Effects 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 description 29
- 125000004432 carbon atom Chemical group C* 0.000 description 25
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 21
- 239000003921 oil Substances 0.000 description 20
- 235000019198 oils Nutrition 0.000 description 20
- -1 fatty acid esters Chemical class 0.000 description 17
- 230000001603 reducing effect Effects 0.000 description 14
- 238000002485 combustion reaction Methods 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 13
- 150000002430 hydrocarbons Chemical group 0.000 description 12
- 239000007789 gas Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 9
- GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 description 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- 125000000753 cycloalkyl group Chemical group 0.000 description 7
- 239000002480 mineral oil Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 125000003342 alkenyl group Chemical group 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 125000004434 sulfur atom Chemical group 0.000 description 6
- 239000010913 used oil Substances 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000003112 inhibitor Substances 0.000 description 5
- 239000003607 modifier Substances 0.000 description 5
- SHMVRUMGFMGYGG-UHFFFAOYSA-N [Mo].S=O Chemical compound [Mo].S=O SHMVRUMGFMGYGG-UHFFFAOYSA-N 0.000 description 4
- 239000010775 animal oil Substances 0.000 description 4
- GVPWHKZIJBODOX-UHFFFAOYSA-N dibenzyl disulfide Chemical compound C=1C=CC=CC=1CSSCC1=CC=CC=C1 GVPWHKZIJBODOX-UHFFFAOYSA-N 0.000 description 4
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 4
- ALVPFGSHPUPROW-UHFFFAOYSA-N dipropyl disulfide Chemical compound CCCSSCCC ALVPFGSHPUPROW-UHFFFAOYSA-N 0.000 description 4
- 150000002019 disulfides Chemical class 0.000 description 4
- 244000144993 groups of animals Species 0.000 description 4
- 125000004492 methyl ester group Chemical group 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 238000007670 refining Methods 0.000 description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 description 4
- 239000008158 vegetable oil Substances 0.000 description 4
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000002877 alkyl aryl group Chemical group 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 235000010290 biphenyl Nutrition 0.000 description 3
- 239000004305 biphenyl Substances 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000000567 combustion gas Substances 0.000 description 3
- 125000002704 decyl group Chemical group [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])* 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000002960 margaryl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 125000001421 myristyl 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])C([H])([H])[H] 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 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 3
- 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 3
- 125000004430 oxygen atom Chemical group O* 0.000 description 3
- 125000000913 palmityl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000002958 pentadecyl 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])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 3
- 239000005077 polysulfide Substances 0.000 description 3
- 229920001021 polysulfide Polymers 0.000 description 3
- 150000008117 polysulfides Polymers 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 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 3
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 3
- 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 3
- AROCLDYPZXMJPW-UHFFFAOYSA-N 1-(octyldisulfanyl)octane Chemical compound CCCCCCCCSSCCCCCCCC AROCLDYPZXMJPW-UHFFFAOYSA-N 0.000 description 2
- 101100422771 Caenorhabditis elegans sup-9 gene Proteins 0.000 description 2
- CETBSQOFQKLHHZ-UHFFFAOYSA-N Diethyl disulfide Chemical compound CCSSCC CETBSQOFQKLHHZ-UHFFFAOYSA-N 0.000 description 2
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 2
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical group CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 125000001204 arachidyl 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])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
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 2
- YSQZSPCQDXHJDJ-UHFFFAOYSA-N di-n-pentyl disulfide Natural products CCCCCSSCCCCC YSQZSPCQDXHJDJ-UHFFFAOYSA-N 0.000 description 2
- WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical compound CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 description 2
- 239000012990 dithiocarbamate Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 125000005456 glyceride group Chemical group 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical group CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 2
- KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical compound C(N)([S-])=S.[Mo+4].C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S KHYKFSXXGRUKRE-UHFFFAOYSA-J 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 125000001196 nonadecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 230000010355 oscillation Effects 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical group CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 2
- 238000005292 vacuum distillation Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 125000005023 xylyl group Chemical group 0.000 description 2
- WYHWGJJOJLOJSZ-UHFFFAOYSA-N (phenyltrisulfanyl)benzene Chemical compound C=1C=CC=CC=1SSSC1=CC=CC=C1 WYHWGJJOJLOJSZ-UHFFFAOYSA-N 0.000 description 1
- IDJPKRIELSFBPE-UHFFFAOYSA-N 1-(decyldisulfanyl)decane Chemical compound CCCCCCCCCCSSCCCCCCCCCC IDJPKRIELSFBPE-UHFFFAOYSA-N 0.000 description 1
- GUBWMRCVCQFLOJ-UHFFFAOYSA-N 1-(hexadecyldisulfanyl)hexadecane Chemical compound CCCCCCCCCCCCCCCCSSCCCCCCCCCCCCCCCC GUBWMRCVCQFLOJ-UHFFFAOYSA-N 0.000 description 1
- GJPDBURPGLWRPW-UHFFFAOYSA-N 1-(hexyldisulfanyl)hexane Chemical compound CCCCCCSSCCCCCC GJPDBURPGLWRPW-UHFFFAOYSA-N 0.000 description 1
- MQQKTNDBASEZSD-UHFFFAOYSA-N 1-(octadecyldisulfanyl)octadecane Chemical compound CCCCCCCCCCCCCCCCCCSSCCCCCCCCCCCCCCCCCC MQQKTNDBASEZSD-UHFFFAOYSA-N 0.000 description 1
- QYVIBJKOSSAQLE-UHFFFAOYSA-N 1-(tridecyldisulfanyl)tridecane Chemical compound CCCCCCCCCCCCCSSCCCCCCCCCCCCC QYVIBJKOSSAQLE-UHFFFAOYSA-N 0.000 description 1
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical class C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- WSDOGTIHAHFYEX-UHFFFAOYSA-J 2-ethylhexoxy-oxido-sulfanylidene-sulfido-lambda5-phosphane molybdenum(4+) sulfur monoxide Chemical compound C(C)C(COP([O-])(=S)[S-])CCCC.O=S.[Mo+4].C(C)C(COP([O-])(=S)[S-])CCCC WSDOGTIHAHFYEX-UHFFFAOYSA-J 0.000 description 1
- OHKYIUYPQIFGKN-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)-3-oxopropanenitrile Chemical compound COC1=CC=CC(C(=O)CC#N)=C1OC OHKYIUYPQIFGKN-UHFFFAOYSA-N 0.000 description 1
- MDWVSAYEQPLWMX-UHFFFAOYSA-N 4,4'-Methylenebis(2,6-di-tert-butylphenol) Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 MDWVSAYEQPLWMX-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- PPZYHXJABUOTCJ-UHFFFAOYSA-J C(=CCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(=CCC)OP([O-])(=S)[S-] Chemical compound C(=CCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(=CCC)OP([O-])(=S)[S-] PPZYHXJABUOTCJ-UHFFFAOYSA-J 0.000 description 1
- GQTSPYQKLKNYGK-UHFFFAOYSA-J C(CC(C)C)NC([S-])=S.O=S.[Mo+4].C(CC(C)C)NC([S-])=S.C(CC(C)C)NC([S-])=S.C(CC(C)C)NC([S-])=S Chemical compound C(CC(C)C)NC([S-])=S.O=S.[Mo+4].C(CC(C)C)NC([S-])=S.C(CC(C)C)NC([S-])=S.C(CC(C)C)NC([S-])=S GQTSPYQKLKNYGK-UHFFFAOYSA-J 0.000 description 1
- DOQNYPIPOJEYML-UHFFFAOYSA-J C(CC)C(CNC([S-])=S)CCC.O=S.[Mo+4].C(CC)C(CNC([S-])=S)CCC.C(CC)C(CNC([S-])=S)CCC.C(CC)C(CNC([S-])=S)CCC Chemical compound C(CC)C(CNC([S-])=S)CCC.O=S.[Mo+4].C(CC)C(CNC([S-])=S)CCC.C(CC)C(CNC([S-])=S)CCC.C(CC)C(CNC([S-])=S)CCC DOQNYPIPOJEYML-UHFFFAOYSA-J 0.000 description 1
- DCKUABUQYGDNNV-UHFFFAOYSA-J C(CCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCC)OP([O-])(=S)[S-] Chemical compound C(CCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCC)OP([O-])(=S)[S-] DCKUABUQYGDNNV-UHFFFAOYSA-J 0.000 description 1
- DAGUOLAXWRRFDI-UHFFFAOYSA-J C(CCCCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCCCC)OP([O-])(=S)[S-] Chemical compound C(CCCCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCCCC)OP([O-])(=S)[S-] DAGUOLAXWRRFDI-UHFFFAOYSA-J 0.000 description 1
- YAXIHUXKRMYGCH-UHFFFAOYSA-J C(CCCCCCCC)NC([S-])=S.O=S.[Mo+4].C(CCCCCCCC)NC([S-])=S.C(CCCCCCCC)NC([S-])=S.C(CCCCCCCC)NC([S-])=S Chemical compound C(CCCCCCCC)NC([S-])=S.O=S.[Mo+4].C(CCCCCCCC)NC([S-])=S.C(CCCCCCCC)NC([S-])=S.C(CCCCCCCC)NC([S-])=S YAXIHUXKRMYGCH-UHFFFAOYSA-J 0.000 description 1
- XOLLAADSZZBOQE-UHFFFAOYSA-J C(CCCCCCCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCCCCCCC)OP([O-])(=S)[S-] Chemical compound C(CCCCCCCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCCCCCCC)OP([O-])(=S)[S-] XOLLAADSZZBOQE-UHFFFAOYSA-J 0.000 description 1
- YOQBPRJNXTUENU-UHFFFAOYSA-J C(CCCCCCCCCCCCCCCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCCCCCCCCCCCCCCC)OP([O-])(=S)[S-] Chemical compound C(CCCCCCCCCCCCCCCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCCCCCCCCCCCCCCC)OP([O-])(=S)[S-] YOQBPRJNXTUENU-UHFFFAOYSA-J 0.000 description 1
- JLMNLOTWPAOKAJ-UHFFFAOYSA-J C(N)([O-])=S.O=S.[Mo+4].C(N)([O-])=S.C(N)([O-])=S.C(N)([O-])=S Chemical class C(N)([O-])=S.O=S.[Mo+4].C(N)([O-])=S.C(N)([O-])=S.C(N)([O-])=S JLMNLOTWPAOKAJ-UHFFFAOYSA-J 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- CUDSBWGCGSUXDB-UHFFFAOYSA-N Dibutyl disulfide Chemical compound CCCCSSCCCC CUDSBWGCGSUXDB-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- MQHWFIOJQSCFNM-UHFFFAOYSA-L Magnesium salicylate Chemical compound [Mg+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O MQHWFIOJQSCFNM-UHFFFAOYSA-L 0.000 description 1
- UVIPMGGWVCXPKY-UHFFFAOYSA-J N-(2-ethylbutyl)carbamodithioate molybdenum(4+) sulfur monoxide Chemical compound C(C)C(CNC([S-])=S)CC.O=S.[Mo+4].C(C)C(CNC([S-])=S)CC.C(C)C(CNC([S-])=S)CC.C(C)C(CNC([S-])=S)CC UVIPMGGWVCXPKY-UHFFFAOYSA-J 0.000 description 1
- OVBFWOPOEWPRLS-UHFFFAOYSA-J N-(2-methyloctadecyl)carbamodithioate molybdenum(4+) sulfur monoxide Chemical compound CC(CNC([S-])=S)CCCCCCCCCCCCCCCC.O=S.[Mo+4].CC(CNC([S-])=S)CCCCCCCCCCCCCCCC.CC(CNC([S-])=S)CCCCCCCCCCCCCCCC.CC(CNC([S-])=S)CCCCCCCCCCCCCCCC OVBFWOPOEWPRLS-UHFFFAOYSA-J 0.000 description 1
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- 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 1
- HHYSHHLEKWFLGQ-UHFFFAOYSA-J P(OCCC)([O-])(=S)[S-].O=S.[Mo+4].C(CC)OP([O-])(=S)[S-] Chemical compound P(OCCC)([O-])(=S)[S-].O=S.[Mo+4].C(CC)OP([O-])(=S)[S-] HHYSHHLEKWFLGQ-UHFFFAOYSA-J 0.000 description 1
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- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical class CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- LUFPJJNWMYZRQE-UHFFFAOYSA-N benzylsulfanylmethylbenzene Chemical compound C=1C=CC=CC=1CSCC1=CC=CC=C1 LUFPJJNWMYZRQE-UHFFFAOYSA-N 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 150000001638 boron Chemical class 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 description 1
- VULUBWFPLUQZFD-UHFFFAOYSA-J butoxy-oxido-sulfanylidene-sulfido-lambda5-phosphane molybdenum(4+) sulfur monoxide Chemical compound C(CCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCC)OP([O-])(=S)[S-] VULUBWFPLUQZFD-UHFFFAOYSA-J 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- AVVIDTZRJBSXML-UHFFFAOYSA-L calcium;2-carboxyphenolate;dihydrate Chemical compound O.O.[Ca+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O AVVIDTZRJBSXML-UHFFFAOYSA-L 0.000 description 1
- ZMRQTIAUOLVKOX-UHFFFAOYSA-L calcium;diphenoxide Chemical compound [Ca+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 ZMRQTIAUOLVKOX-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- FJCJVVNXCKMOOP-UHFFFAOYSA-J dodecoxy-oxido-sulfanylidene-sulfido-lambda5-phosphane molybdenum(4+) sulfur monoxide Chemical compound C(CCCCCCCCCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCCCCCCCCC)OP([O-])(=S)[S-] FJCJVVNXCKMOOP-UHFFFAOYSA-J 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- ZQRSQKSUPJBTBT-UHFFFAOYSA-J hexoxy-oxido-sulfanylidene-sulfido-lambda5-phosphane molybdenum(4+) sulfur monoxide Chemical compound C(CCCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCCC)OP([O-])(=S)[S-] ZQRSQKSUPJBTBT-UHFFFAOYSA-J 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000006317 isomerization reaction Methods 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
- 229940072082 magnesium salicylate Drugs 0.000 description 1
- KRPXAHXWPZLBKL-UHFFFAOYSA-L magnesium;diphenoxide Chemical compound [Mg+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 KRPXAHXWPZLBKL-UHFFFAOYSA-L 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- OZFOEEDAMPGQDB-UHFFFAOYSA-J molybdenum(4+) N-(2-propylhexyl)carbamodithioate sulfur monoxide Chemical compound C(CC)C(CNC([S-])=S)CCCC.O=S.[Mo+4].C(CC)C(CNC([S-])=S)CCCC.C(CC)C(CNC([S-])=S)CCCC.C(CC)C(CNC([S-])=S)CCCC OZFOEEDAMPGQDB-UHFFFAOYSA-J 0.000 description 1
- PFANWDKTZYAONO-UHFFFAOYSA-J molybdenum(4+) N-octadecylcarbamodithioate sulfur monoxide Chemical compound C(CCCCCCCCCCCCCCCCC)NC([S-])=S.O=S.[Mo+4].C(CCCCCCCCCCCCCCCCC)NC([S-])=S.C(CCCCCCCCCCCCCCCCC)NC([S-])=S.C(CCCCCCCCCCCCCCCCC)NC([S-])=S PFANWDKTZYAONO-UHFFFAOYSA-J 0.000 description 1
- OKVXVKMNSMHPIP-UHFFFAOYSA-J molybdenum(4+) octoxy-oxido-sulfanylidene-sulfido-lambda5-phosphane sulfur monoxide Chemical compound C(CCCCCCC)OP([O-])(=S)[S-].O=S.[Mo+4].C(CCCCCCC)OP([O-])(=S)[S-] OKVXVKMNSMHPIP-UHFFFAOYSA-J 0.000 description 1
- BCBHLWYLGWJAJF-UHFFFAOYSA-J molybdenum(4+) sulfur monoxide tetracarbamodithioate Chemical class [Mo+4].S=O.NC([S-])=S.NC([S-])=S.NC([S-])=S.NC([S-])=S BCBHLWYLGWJAJF-UHFFFAOYSA-J 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 150000008301 phosphite esters Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
- MBBWTVUFIXOUBE-UHFFFAOYSA-L zinc;dicarbamodithioate Chemical class [Zn+2].NC([S-])=S.NC([S-])=S MBBWTVUFIXOUBE-UHFFFAOYSA-L 0.000 description 1
Classifications
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- 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
- C10M141/10—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 at least one of them being an organic phosphorus-containing compound
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- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
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- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/08—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium containing a sulfur-to-oxygen bond
- C10M135/10—Sulfonic acids or derivatives thereof
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- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/12—Thio-acids; Thiocyanates; Derivatives thereof
- C10M135/14—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond
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- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/12—Thio-acids; Thiocyanates; Derivatives thereof
- C10M135/14—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond
- C10M135/18—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond thiocarbamic type, e.g. containing the groups
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- C10M135/22—Thiols; Sulfides; Polysulfides containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
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- C10M135/26—Thiols; Sulfides; Polysulfides containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing carboxyl groups; Derivatives thereof
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- C10M135/28—Thiols; Sulfides; Polysulfides containing sulfur atoms bound to a carbon atom of a six-membered aromatic ring
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- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/20—Thiols; Sulfides; Polysulfides
- C10M135/28—Thiols; Sulfides; Polysulfides containing sulfur atoms bound to a carbon atom of a six-membered aromatic ring
- C10M135/30—Thiols; Sulfides; Polysulfides containing sulfur atoms bound to a carbon atom of a six-membered aromatic ring containing hydroxy groups; Derivatives thereof
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- C10M135/32—Heterocyclic sulfur, selenium or tellurium compounds
- C10M135/36—Heterocyclic sulfur, selenium or tellurium compounds the ring containing sulfur and carbon with nitrogen or oxygen
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- 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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- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
- C10M159/22—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing phenol radicals
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- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
- C10M159/24—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing sulfonic radicals
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- C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/04—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing aromatic monomers, e.g. styrene
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/06—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing conjugated dienes
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
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- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/108—Phenothiazine
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
-
- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/041—Siloxanes with specific structure containing aliphatic substituents
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/12—Groups 6 or 16
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2060/00—Chemical after-treatment of the constituents of the lubricating composition
- C10N2060/04—Oxidation, e.g. ozonisation
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Lubrication Of Internal Combustion Engines (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22046296A JP3497952B2 (ja) | 1996-08-02 | 1996-08-02 | 潤滑油組成物 |
Publications (2)
Publication Number | Publication Date |
---|---|
DE69703226D1 DE69703226D1 (de) | 2000-11-09 |
DE69703226T2 true DE69703226T2 (de) | 2001-03-15 |
Family
ID=16751502
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE69703226T Expired - Fee Related DE69703226T2 (de) | 1996-08-02 | 1997-07-30 | Schmierölzusammensetzung |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0822246B1 (es) |
JP (1) | JP3497952B2 (es) |
AU (1) | AU718688B2 (es) |
CA (1) | CA2210974C (es) |
DE (1) | DE69703226T2 (es) |
ES (1) | ES2153161T3 (es) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11269477A (ja) * | 1998-03-20 | 1999-10-05 | Cosmo Sogo Kenkyusho Kk | エンジン油組成物 |
KR101083151B1 (ko) * | 2003-02-05 | 2011-11-11 | 이데미쓰 고산 가부시키가이샤 | 윤활유 및 연료유용 첨가제, 윤활유 조성물 및 연료유조성물 |
JP4563082B2 (ja) * | 2004-06-03 | 2010-10-13 | 出光興産株式会社 | 潤滑油基油及び潤滑油組成物 |
JP5175462B2 (ja) | 2006-09-04 | 2013-04-03 | 出光興産株式会社 | 内燃機関用潤滑油組成物 |
JP5468728B2 (ja) | 2007-05-29 | 2014-04-09 | 出光興産株式会社 | 内燃機関用潤滑油組成物 |
EP2231681B1 (en) * | 2007-12-14 | 2013-11-06 | Vanderbilt Chemicals, LLC | Additive composition for ep greases with excellent antiwear and corrosion properties |
US20100152074A1 (en) * | 2008-12-17 | 2010-06-17 | Chevron Oronite Company Llc | Lubricating oil compositions |
US20100152072A1 (en) * | 2008-12-17 | 2010-06-17 | Chevron Oronite Company Llc | Lubricating oil compositions |
FR2990213B1 (fr) | 2012-05-04 | 2015-04-24 | Total Raffinage Marketing | Composition lubrifiante pour moteur |
FR2998303B1 (fr) | 2012-11-16 | 2015-04-10 | Total Raffinage Marketing | Composition lubrifiante |
CN109652171B (zh) * | 2017-10-12 | 2021-12-14 | 中国石油化工股份有限公司 | 一种工业机器人关节rv减速机专用油组合物 |
CN114686189B (zh) * | 2022-04-22 | 2023-10-20 | 中国石油天然气集团有限公司 | 水基钻井液用润滑剂及其制备方法以及水基钻井液 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06200270A (ja) * | 1992-12-29 | 1994-07-19 | Tonen Corp | 終減速機用潤滑油組成物 |
CA2195475A1 (en) * | 1994-09-01 | 1996-03-07 | Michiya Yamada | Lubricants with sustained fuel economy performance |
JP2971748B2 (ja) * | 1994-09-05 | 1999-11-08 | 株式会社ジャパンエナジー | エンジン油組成物 |
-
1996
- 1996-08-02 JP JP22046296A patent/JP3497952B2/ja not_active Expired - Lifetime
-
1997
- 1997-07-30 EP EP97305728A patent/EP0822246B1/en not_active Expired - Lifetime
- 1997-07-30 ES ES97305728T patent/ES2153161T3/es not_active Expired - Lifetime
- 1997-07-30 DE DE69703226T patent/DE69703226T2/de not_active Expired - Fee Related
- 1997-07-30 CA CA002210974A patent/CA2210974C/en not_active Expired - Fee Related
- 1997-07-31 AU AU32421/97A patent/AU718688B2/en not_active Ceased
Also Published As
Publication number | Publication date |
---|---|
ES2153161T3 (es) | 2001-02-16 |
CA2210974C (en) | 2004-09-14 |
EP0822246A2 (en) | 1998-02-04 |
EP0822246B1 (en) | 2000-10-04 |
CA2210974A1 (en) | 1998-02-02 |
DE69703226D1 (de) | 2000-11-09 |
AU3242197A (en) | 1998-02-12 |
EP0822246A3 (en) | 1998-04-15 |
JPH1046177A (ja) | 1998-02-17 |
JP3497952B2 (ja) | 2004-02-16 |
AU718688B2 (en) | 2000-04-20 |
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