WO2007120712A2 - Additif et composition lubrifiants pour moteur à faible taux de soufre, de cendre et de phosphore contenant du soufre non corrosif et des borates organiques - Google Patents
Additif et composition lubrifiants pour moteur à faible taux de soufre, de cendre et de phosphore contenant du soufre non corrosif et des borates organiques Download PDFInfo
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- WO2007120712A2 WO2007120712A2 PCT/US2007/008946 US2007008946W WO2007120712A2 WO 2007120712 A2 WO2007120712 A2 WO 2007120712A2 US 2007008946 W US2007008946 W US 2007008946W WO 2007120712 A2 WO2007120712 A2 WO 2007120712A2
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- 239000000203 mixture Substances 0.000 title claims abstract description 105
- 239000000654 additive Substances 0.000 title claims abstract description 95
- 230000000996 additive effect Effects 0.000 title claims abstract description 60
- 229910052717 sulfur Inorganic materials 0.000 title claims abstract description 59
- 239000011593 sulfur Substances 0.000 title claims abstract description 58
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 title claims abstract description 57
- 230000009972 noncorrosive effect Effects 0.000 title claims description 33
- 239000010705 motor oil Substances 0.000 title description 26
- 150000001642 boronic acid derivatives Chemical class 0.000 title description 9
- 239000010687 lubricating oil Substances 0.000 claims abstract description 22
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 17
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000011574 phosphorus Substances 0.000 claims abstract description 16
- 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 claims abstract description 16
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910052796 boron Inorganic materials 0.000 claims abstract description 13
- 238000000034 method Methods 0.000 claims abstract description 12
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 12
- 239000011701 zinc Substances 0.000 claims abstract description 12
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 230000002349 favourable effect Effects 0.000 claims abstract description 11
- 239000003112 inhibitor Substances 0.000 claims abstract description 9
- 230000001050 lubricating effect Effects 0.000 claims abstract description 6
- 239000003963 antioxidant agent Substances 0.000 claims description 21
- 235000006708 antioxidants Nutrition 0.000 claims description 19
- 239000002270 dispersing agent Substances 0.000 claims description 18
- 239000000314 lubricant Substances 0.000 claims description 17
- 239000003599 detergent Substances 0.000 claims description 16
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 15
- -1 polyol esters Chemical class 0.000 claims description 14
- 230000003647 oxidation Effects 0.000 claims description 12
- 238000007254 oxidation reaction Methods 0.000 claims description 12
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 7
- 230000003749 cleanliness Effects 0.000 claims description 7
- 229910052750 molybdenum Inorganic materials 0.000 claims description 7
- 239000011733 molybdenum Substances 0.000 claims description 7
- 239000012990 dithiocarbamate Substances 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- HAXFWIACAGNFHA-UHFFFAOYSA-N aldrithiol Chemical compound C=1C=CC=NC=1SSC1=CC=CC=N1 HAXFWIACAGNFHA-UHFFFAOYSA-N 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 150000004659 dithiocarbamates Chemical class 0.000 claims description 4
- 125000001741 organic sulfur group Chemical group 0.000 claims description 4
- 150000004867 thiadiazoles Chemical class 0.000 claims description 4
- BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 claims description 3
- PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 claims description 3
- 238000002485 combustion reaction Methods 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 239000003607 modifier Substances 0.000 claims description 3
- 229920005862 polyol Polymers 0.000 claims description 3
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 claims description 3
- AFSHUZFNMVJNKX-CLFAGFIQSA-N 1,2-dioleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCC\C=C/CCCCCCCC AFSHUZFNMVJNKX-CLFAGFIQSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 239000007866 anti-wear additive Substances 0.000 claims description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims description 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims description 2
- 229940071160 cocoate Drugs 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 229920000768 polyamine Polymers 0.000 claims description 2
- 150000003900 succinic acid esters Chemical class 0.000 claims description 2
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 2
- GVIJJXMXTUZIOD-UHFFFAOYSA-N thianthrene Chemical compound C1=CC=C2SC3=CC=CC=C3SC2=C1 GVIJJXMXTUZIOD-UHFFFAOYSA-N 0.000 claims description 2
- 239000003879 lubricant additive Substances 0.000 claims 6
- GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 claims 2
- 125000005233 alkylalcohol group Chemical group 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- AVWMIWJCGFMMNP-UHFFFAOYSA-N 1-(nonyldisulfanyl)nonane Chemical compound CCCCCCCCCSSCCCCCCCCC AVWMIWJCGFMMNP-UHFFFAOYSA-N 0.000 claims 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 claims 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims 1
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000004034 viscosity adjusting agent Substances 0.000 claims 1
- 239000003921 oil Substances 0.000 abstract description 64
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 abstract description 12
- 239000002585 base Substances 0.000 description 60
- 239000002199 base oil Substances 0.000 description 34
- 230000000052 comparative effect Effects 0.000 description 20
- 238000005260 corrosion Methods 0.000 description 19
- 239000000463 material Substances 0.000 description 18
- 239000001993 wax Substances 0.000 description 18
- 230000007797 corrosion Effects 0.000 description 17
- 238000009472 formulation Methods 0.000 description 15
- 238000012360 testing method Methods 0.000 description 15
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 11
- 229910052802 copper Inorganic materials 0.000 description 11
- 239000010949 copper Substances 0.000 description 11
- 230000008901 benefit Effects 0.000 description 8
- 230000009467 reduction Effects 0.000 description 8
- 125000004122 cyclic group Chemical group 0.000 description 6
- GVPWHKZIJBODOX-UHFFFAOYSA-N dibenzyl disulfide Chemical compound C=1C=CC=CC=1CSSCC1=CC=CC=C1 GVPWHKZIJBODOX-UHFFFAOYSA-N 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 150000002430 hydrocarbons Chemical group 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 230000006872 improvement Effects 0.000 description 5
- 231100000241 scar Toxicity 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 4
- 230000003064 anti-oxidating effect Effects 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229920002367 Polyisobutene Polymers 0.000 description 3
- 150000004982 aromatic amines Chemical class 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 229920013639 polyalphaolefin Polymers 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
- 150000007970 thio esters Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910001868 water Inorganic materials 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000003042 antagnostic effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 230000007096 poisonous effect Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 229960002317 succinimide Drugs 0.000 description 2
- 150000003464 sulfur compounds Chemical class 0.000 description 2
- 239000011885 synergistic combination Substances 0.000 description 2
- KMKSVAGOBVUFRO-UHFFFAOYSA-N 1-nonylsulfanylnonane Chemical compound CCCCCCCCCSCCCCCCCCC KMKSVAGOBVUFRO-UHFFFAOYSA-N 0.000 description 1
- 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 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
- UHBAPGWWRFVTFS-UHFFFAOYSA-N 4,4'-dipyridyl disulfide Chemical compound C=1C=NC=CC=1SSC1=CC=NC=C1 UHBAPGWWRFVTFS-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
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- MQHWFIOJQSCFNM-UHFFFAOYSA-L Magnesium salicylate Chemical class [Mg+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O MQHWFIOJQSCFNM-UHFFFAOYSA-L 0.000 description 1
- 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
- 229910019142 PO4 Inorganic materials 0.000 description 1
- XYRMLECORMNZEY-UHFFFAOYSA-B [Mo+4].[Mo+4].[Mo+4].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S Chemical class [Mo+4].[Mo+4].[Mo+4].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S XYRMLECORMNZEY-UHFFFAOYSA-B 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- VBIGULIJWJPALH-UHFFFAOYSA-L calcium;2-carboxyphenolate Chemical class [Ca+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O VBIGULIJWJPALH-UHFFFAOYSA-L 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 125000005044 dihydroquinolinyl group Chemical group N1(CC=CC2=CC=CC=C12)* 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 150000002193 fatty amides Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical class C(N)([S-])=S.[Mo+4].C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S KHYKFSXXGRUKRE-UHFFFAOYSA-J 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- QAUCEEIOCLCCFG-UHFFFAOYSA-N trihydroxy borate Chemical class OOB(OO)OO QAUCEEIOCLCCFG-UHFFFAOYSA-N 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical class [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 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
- C10M141/12—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 compound containing atoms of elements not provided for in groups C10M141/02 - C10M141/10
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions used as base material
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
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Definitions
- This invention relates to lubricating oil compositions suitable for use in internal combustion engines. More particularly, this invention relates to a low ash, sulfur, and phosphorous lubricating oil composition.
- Contemporary lubricants such as engine oils use mixtures of additive components to include numerous performances benefits.
- additives components include, anti-wear and extreme pressure components, fuel economy improving components, friction reducers, dispersants, detergents, corrosion inhibitors and viscosity index improving additive. These additives provide energy conservation, engine cleanliness and durability and high performance levels to the lubricating oil under a wide range of engine operability conditions including temperature, pressure and lubricant service life.
- ZnDTP zinc (dialkyl) dithiophosphate
- ZnDDP zinc (dialkyl) dithiophosphate
- Sulfur is known to be poisonous to deNox catalysts and zinc phosphates cause plugging of the exhaust particulate filters.
- SAP sulfur, ash and phosphorous components in oil are commonly referred to as "SAP" or "SAPS" in the art.
- ZnDTP The major problem with ZnDTP is the poisoning effects to after- treatment devices that may aggravate emission problems.
- ZnDTP has strong interactions with dispersants, detergents, other anti-wear components and MoDTC causing antagonistic effects on friction, sludge and deposit, if inappropriate concentrations are utilized.
- Replacing ZnDTP additives is not a simple endeavor because the wear protection demand for today's engine is extremely high and place extremely rigorous chemical limits on any reductions in ZnDTP treat levels.
- a lubricating oil composition comprises a lubricating oil basestock, a boron-containing additive present in the amount in the range of at least 0.1 weight percent of the composition and less than 8.0 weight percent, a non-corrosive sulfur additive present in the amount in the range of at least 0.1 weight percent of the composition and less than 4.0 weight percent , a dispersant— detergent-inhibitor system of less than 15 percent weight percent of the composition, a zinc dithiophosphate additive present in the amount in the range of at least 0.2 weight percent of the composition and no more than 2.0 weight percent of the composition wherein weight percent is active ingredient weight of the composition.
- the formulated oil composition having at least 100 and less than 630 PPM phosphorus, at least 1,000 PPM and less than 3,000 PPM sulfur, and at least 105 PPM and less than 710 PPM zinc, at least 80 PPM and less than 450 PPM boron.
- an additive composition for lubricating oils comprises an organic boron containing additive present in the amount in the range of at least 0.4 weight percent and less than 32 weight percent of the additive, a detergent-dispersant system of less than 60 percent weight percent of the additive, a zinc dithiophosphate additive present in the amount in the range of at least 0.8 weight percent and less than 8.0 weight percent of the additive, a non-corrosive ashless sulfur additive present in the amount in the range of at 0.4 and less than 16.0 weight percent of the additive.
- a method of obtain a favorable lubricating properties comprises obtaining a composition comprising a lubricating oil basestock, an organic boron containing additive of at least 0.1 and less than 8 weight percent of the composition, a dispersant— detergent- inhibitor system of less than 15 percent weight percent of the composition, zinc dithiophosphate additive of at least 0.2 weight percent of the composition and no more than 2.0 weight percent of the composition, a non corrosive ashless sulfur additive of at 0.1 and less than 4.0 weight percent of the 08946
- the formulated oil composition having at least 100 and less than 630 PPM phosphorus, at least 1,000 PPM and less than 3,000 PPM sulfur, and at least 105 PPM and less than 710 PPM zinc, at least 80 PPM and less than 450 PPM boron.
- This invention relates to engine lubricants formulated with unique functional fluids and/or additives to achieve performance improvements.
- One embodiment is a low SAP engine lubricant composition comprising combinations of organic borates, non-corrosive sulfur compounds, optional high levels of ashless antioxidants, and low levels of ZnDTP to achieve high level of performance equal to or better than using high level of ZnDTP alone.
- component synergy is built upon a variety of functionalities to achieve well balanced performance features. In a preferred embodiment, these performance features favorably exceed engine oils formulated with high levels of zinc dithiophosphates and metallic detergents.
- the lubricating oils maintain low frictional properties of film under various operating conditions.
- This embodiment favorably maintains sufficiently high film thickness at high operating temperatures to provide a minimum lubricant film to protect against wear at a variety of temperatures.
- the lubricating oil maintains cleanliness over the entire range of operating conditions while reducing wear to a minimum.
- the lubricating oil provides favorable oxidation and corrosion control, under the most severe operating conditions.
- non-corrosive, organic sulfur compounds when blended with high levels of organic borates, and low level of zinc dithiophosphates provide substantial property benefits.
- high levels of ashless antioxidants are added to the compounds to achieve even more favorable property benefits. These benefits include but are not limited to reductions in wear, corrosion, and increases in oil induction temperature or time (OIT) during oxidative conditions that result in potentially significant improvements in engine oil service life and durability with excellent overall performance benefits.
- these benefits can be achieved without deleterious effects such as instability, undesirable high viscosity, deposits and the like, when the additives are added to lubricating oils.
- This new engine oil technology is based on an advanced anti-wear, anti-friction and antioxidant system, in combination of some typical, contemporary dispersants, ashless antioxidants, detergents, defoamants and other additives including contemporary DI additive packages. These additives enhance anti- wear, anti-oxidation and anti-corrosion performance.
- the preferred organic borates are borated hydroxyl esters, such as borated glycerol .mono-oleate (GMO), borated glycerol di-oleate (GDO), borated glycerol tri-oleate (GTO), borated glycerol mono-cocoate (GMC), borated mono-talloate (GMT), borated glycerol mono-sorbitate (GMS), borated polyol esters with pendant hydroxyl groups, such as borated pentaerythritol di-C8 ester, and any combination thereof.
- GMO borated glycerol .monoleate
- GDO borated glycerol di-oleate
- GTO borated glycerol tri-oleate
- GMC borated glycerol mono-cocoate
- GTT mono-talloate
- GMS borated polyol esters with pendant hydroxyl groups, such as borated pentaerythri
- Short chain tri-hydroxyl orthoborates may be used but are not desirable due to their relatively poor thermal/oxidative stability properties when compared to borated hydroxyl esters.
- Borated dispersants and borated detergents can be used as a source of boron.
- specific organic borates, such as borated hydroxyl esters are more preferable.
- the preferred non-corrosive sulfur compounds are chosen from the group consisting of ashless derivatives of thiadiazoles, ashless derivatives of benzothiazoles, ashless alkyl or aryl sulfides and poly sulfides, for example, disulfides and tri-sulfide including thianthrene and its alkylates, diphenyl sulfide and disulfide, and their alkylates, dinonyl sulfide or disulfide, dipyridyl sulfide or disulfide, and their alkylates, ashless dithiocarbamates, and thioesters/sulfurized esters including thioglycolates, dialkyl thiodipropionates, dialkyl dithiopropionates.
- ashless thiadiazoles are Vanlube 871TM, Cuvan 826TM and Cuvan 484TM.
- Examples of ashless dithiocarbamates are Vanlube 7723TM and Vanlube 981.
- a prerequisite to the selection of sulfur additives is that they all need to meet copper corrosion requirements according to ASTM (D 130) and low temperature storage compatibility tests.
- the anti-corrosion performance can be judged by the copper corrosion test ASTDM D130 under normal conditions.
- ASTDM test D130-6 normal conditions are at 250 degrees Fahrenheit at 3 hours.
- ASTDM test D130-8 normal conditions are set at 210 degrees Fahrenheit for 6 hours with percent 46
- non-corrosive sulfur shall be defined as any sulfur that provides a performance classification of 2B or better under the ASTM D- 130 Copper Corrosion Test.
- Dibenzyl disulfide was deficient in a severe copper corrosion test at degrees Fahrenheit for 24 hours and 2,2'-dipyridyl disulfide has poor low temperature compatibility in engine oils. Therefore, both additives are deemed less favorable, despite of their strong EP performance. Sulfur additives containing a small portion of polysulfides (tri-sulfide/tetra-sulf ⁇ de and higher order of polysulfides) are still acceptable providing that they could meet the copper corrosion requirements.
- the preferred ashless antioxidants are hindered phenols and arylamines. Typical examples are butylated/octylated/styrenated/nonylated/ dodecylated diphenyl amines, 4,4'-methylene bis-(2,6-di-tert-butylphenol), 2,6- di-tert-butyl-p-cresol, octylated phenyl-alpha-naphthylamine, alkyl ester of 3,5- di-tert-butyl-4-hydroxy-phenyl propionic acid, and many others. Sulfur- containing antioxidants, such as sulfur linked hindered phenols and thiol esters can also be used.
- Suitable dispersants include borated and non-borated succinimides, succinic acid-esters and amides, alkylphenol-polyamine coupled Mannich adducts, other related components and any combination thereof. In some embodiments, it can often be advantageous to use mixtures of such above described dispersants and other related dispersants.
- Examples include additives that are borated, those that are primarily of higher molecular weight, those that consist of primarily mono-succinimide, bis-succinimide, or mixtures of above, those made with different amines, those that are end-capped, dispersants wherein the back-bone is derived from polymerization of branched olefins such as polyisobutylene or from polymers such as other polyolefins other than polyisobutylene, such as ethylene, propylene, butene, similar dispersants and any combination thereof.
- the averaged molecular weight of the hydrocarbon backbone of most dispersants, including polyisobutylene is in the range from 1000 to 6000, preferably from 1500 to 3000 and most preferably around 2200.
- Suitable detergents include but are not limited to calcium phenates, calcium sulfonates, calcium salicylates, magnesium phenates, magnesium sulfonates, magnesium salicylates, metal carbonates, related components including borated detergents, and any combination thereof.
- the detergents can be neutral, mildly overbased, or highly overbased.
- the amount of detergents usually contributes a total base number (TBN) in a range from 1 to 9 for the formulated lubricant composition.
- Metal detergents have been chosen from alkali or alkaline earth calcium or magnesium phenates, sulfonates, salicylates, carbonates and similar components.
- Antioxidants have been chosen from hindered phenols, arylamines, dihydroquinolines, phosphates, thiol/thiolester/disulfide/trisulfide, low sulfur peroxide decomposers and other related components. These additives are rich in sulfur, phosphorus and/or ash content as they form strong chemical films to the metal surfaces and thus need to be used in limited amount in reduced sulfur, ash and phosphorous lubricating oils.
- Base stocks having a high paraffinic/naphthenic and saturation nature of greater than 90 weight percent can often be used advantageously in certain embodiments.
- Such base stocks include Group II and/or Group III hydroprocessed or hydrocracked base stocks, or their synthetic counterparts such as polyalphaolefin oils, GTL or similar base oils or mixtures of similar base oils.
- At least about 20 percent of the total composition should consist of such Group II or Group III base stocks or GTL, with at least about 30 percent being preferable, and more than about 80 percent on being most preferable.
- Gas to liquid base stocks can also be preferentially used with the components of this invention as a portion or all of the base stocks used to formulate the finished lubricant.
- GTL materials are materials that are derived via one or more synthesis, combination, transformation, rearrangement, and/or degradation/deconstructive processes from gaseous carbon-containing compounds, hydrogen-containing compounds, and/or elements as feedstocks such as hydrogen, carbon dioxide, carbon monoxide, water, methane, ethane, ethylene, acetylene, propane, propylene, propyne, butane, butylenes, and butynes.
- GTL base stocks and base oils are GTL materials of lubricating viscosity that are generally derived from hydrocarbons, for example waxy synthesized hydrocarbons, that are themselves derived from simpler gaseous carbon-containing compounds, hydrogen-containing compounds and/or elements as feedstocks.
- GTL base stock(s) include oils boiling in the lube oil boiling range separated/fractionated from GTL materials such as by, for example, distillation or thermal diffusion, and subsequently subjected to well-known catalytic or solvent dewaxing processes to produce lube oils of reduced/low pour point; wax isomerates, comprising, for example, hydroisomerized or isodewaxed synthesized hydrocarbons; hydroisomerized or isodewaxed Fischer-Tropsch ("F- T") material (i.e., hydrocarbons, waxy hydrocarbons, waxes and possible analogous oxygenates); preferably hydroisomerized or isodewaxed F-T hydrocarbons or hydroisomerized or isodewaxed F-T waxes, hydroisomerized or isodewaxed synthesized waxes, or mixtures thereof.
- F- T Fischer-Tropsch
- GTL base stock(s) derived from GTL materials especially, hydroisomerized/isodewaxed F-T material derived base stock(s), and other hydroisomerized/isodewaxed wax derived base stock(s) are characterized typically as having kinematic viscosities at 100 0 C of from about 2 mm 2 /s to about 50 mm 2 /s, preferably from about 3 mm 2 /s to about 50 mm 2 /s, more preferably from about 3.5 mm /s to about 30 mm /s, as exemplified by a GTL base stock derived by the isodewaxing of F-T wax, which has a kinematic viscosity of about 4 mm 2 /s at 100 0 C and a viscosity index of about 130 or greater.
- GTL base oil/base stock and/or wax isomerate base oil/base stock as used herein and in the claims is to be understood as embracing individual fractions of GTL base stock/base oil or wax isomerate base stock/base oil as recovered in the production process, mixtures of two or more GTL base stocks/base oil fractions and/or wax isomerate base stocks/base oil fractions, as well as mixtures of one or two or more low viscosity GTL base stock(s)/base oil fraction(s) and/or wax isomerate base stock(s)/base oil fraction(s) with one, two or more high viscosity GTL base stock(s)/base oil fraction(s) and/or wax isomerate base stock(s)/base oil fraction(s) to produce a dumbbell blend wherein the blend exhibits a viscosity within the aforesaid recited range.
- Kinematic viscosity refers to a measurement made by ASTM method D445.
- GTL base stocks and base oils derived from GTL materials are further characterized typically as having pour points of about -5°C or lower, preferably about -10 0 C or lower, more preferably about -15°C or lower, still more preferably about -20 0 C or lower, and under some conditions may have advantageous pour points of about -25°C or lower, with useful pour points of about -30 0 C to about -40 0 C or lower. If necessary, a separate dewaxing step may be practiced to achieve the desired pour point.
- pour point refer to measurement made by ASTM D97 and similar automated versions. 46
- the GTL base stock(s) derived from GTL materials, especially hydroisomerized/isodewaxed F-T material derived base stock(s), and other hydroisomerized/isodewaxed wax-derived base stock(s) which are base stock components which can be used in this invention are also characterized typically as having viscosity indices of 80 or greater, preferably 100 or greater, and more preferably 120 or greater. Additionally, in certain particular instances, viscosity index of these base stocks may be preferably 130 or greater, more preferably 135 or greater, and even more preferably 140 or greater.
- GTL base stock(s) that derive from GTL materials preferably F-T materials especially F-T wax generally have a viscosity index of 130 or greater. References herein to viscosity index refer to ASTM method D2270.
- the GTL base stock(s) are typically highly paraffinic of greater than 90 percent saturates), and may contain mixtures of monocycloparaffins and multicycloparaffins in combination with non-cyclic isoparaffins.
- the ratio of the naphthenic (i.e., cycloparaffin) content in such combinations varies with the catalyst and temperature used.
- GTL base stocks and base oils typically have very low sulfur and nitrogen content, generally containing less than about 10 ppm, and more typically less than about 5 ppm of each of these elements.
- the sulfur and nitrogen content of GTL base stock and base oil obtained by the hydroisomerization/isodewaxing of F-T material, especially F-T wax is essentially nil.
- the GTL base stock(s) comprises paraffinic materials that consist predominantly of non-cyclic isoparaffins and only minor amounts of cycloparaffins.
- These GTL base stock(s) typically comprise paraffinic materials that consist of greater than 60 wt% non-cyclic isoparaffins, preferably greater than 80 wt% non-cyclic isoparaffins, more preferably greater than 85 wt% non-cyclic isoparaffins, and most preferably greater than 90 wt% non-cyclic isoparaffins.
- compositions of GTL base stock(s), hydroisomerized or isodewaxed F-T material derived base stock(s), and wax-derived hydroisomerized/isodewaxed base stock(s), such as wax isomerates/isodewaxates are recited in U.S. Pat. Nos. 6,080,301; 6,090,989, and 6,165,949 for example.
- the principle advantage of one embodiment of this invention is the unique synergistic combination of organic borates, non-corrosive sulfur additives in the presence of low level zinc dithiophosphates and high level of ashless antioxidants that provides favorable oxidation, corrosion stability, and more importantly, anti-wear performance. These favorable performance levels can be achieved while reducing the levels of sulfur, phosphorus and zinc in the engine oil formulations compared to the typical engine oil used today.
- Table 3 illustrates low temperature stabilities for different ashless antiwear additives for low phosphorous lubricant oils with a phosphorous level of 0.05 weight percent of the composition.
- Table 3 illustrates various embodiments for two reference base oils formulations. Both base Reference oils A and B are formulated with the premium Group III base oils.
- comparative oils 1, 2, 3 and 4 are variations of reference oil A.
- the formulation for reference oil A is disclosed in Table 4.
- comparative oil 5 is a variations of reference oil B.
- the formulation for reference oil B is disclosed in Table 5.
- Table 3 also illustrates copper corrosion test from the ASTM D- 130 method.
- Table 6 illustrates the various classifications from the ASTDM Copper Corrosion test. As shown in table 6, Classifications IA, IB, 2A, and 2B are the non-corrosive preferred classifications with classifications 2C, 2D, 2,E. 3A, 3B, 4A, 4B, and 4C being the non preferred classifications.
- Reference oil B is a ZnDTP free blend developed so different amounts of ZnDTP as well as other non-corrosive organic sulfur additives can be added to show comparative performance results.
- the base formulation is formulated with Group III base oils with a minimum of 120 viscosity index, a typical pour point of -15°C, a typical Noack of 15 and a typical sulfur of 10 ppm with a miximum sulfur content less than 30 ppm.
- the base engine oil formulated is also formulated with GTL oils with a minimum of 135 viscosity index, a typical pour point of -17°C and a typical sulfur of less than 1 ppm.
- Table 7 illustrates that very good oxidation/corrosion control can be achieved with combinations of non-corrosive sulfur additives, borated dispersants, high level of ashless antioxidants and low level of zinc dithiophosphates in a low Phosphorus engine oil.
- Columns one and two represent reference oils C and D and Columns 3, 4 and 5 represent respectively comparative oils 6, 7, and 8 which are variation of reference oil D.
- Reference oil C is a low SAP group III base oil with 0.1 weight percent phosphorous.
- reference oil D and example comparative oils 6, 7, and 8 are Group III low SAP base oils with 0.05 weight percent phosphorous. Slight variations in the formulations are also documented in Table 7.
- the non-corrosive sulfur additives in comparative example embodiment oil 6 is an ashless dithiocarbamates ("DTC") called VanlubeTM981.
- VanlubeTM981 is an experimental additive avsailable from R.T. Vanderbilt Chemical Company.
- Comparative oils 7 and 8 are specific sulfurized ester/olefins with low sulfur content with or without DTC as in comparative oils 7 and 8 and are respectively labeled RC-2411 and RC-2515.
- RC-2411 and RC- 2515 are commercially available from Rhein Chemie Chemical Company]
- the good corrosion control is evidenced by IA to 2B copper corrosion ratings under various conditions.
- the anti-oxidation performance of oils 6, 7, and 8 are slightly better than reference oil D.
- example comparison oils 6, 7, and 8 formulated with 0.05% phosphorus plus non- corrosive sulfur additives provide favorable performance when compared to a typical engine oil, with full load of ZDDP as in the 1 weight percent reference oil C. This demonstrates the strong synergistic effect exists of the various embodiments of example oils 6, 7, and 8. All the additive components of examples 6, 7, and 8 are fully compatible with engine oils as evidenced by their clear and bright appearance in storage over a period of several months.
- Table 7 demonstrates satisfactory stability for oils containing non-corrosive sulfur additives. Lastly, the pin-on-. V block shown as Falex wear test results correlate well with 4-Ball wear/EP results indicating better wear control with comparative oils 6 and 7 versus Reference oil D.
- Table 9 illustrates the evaluation of non-corrosive sulfur additives in low SAP commercial vehicle lubricants ("CVL"). Table 9 is formulated with a low SAP base oil with no phosphorous.
- a 0.3 weight percent of a non-corrosive sulfur additive in this example an ashless dithiocarbamate, is included in the engine oil formulated with 0.03 weight percent phosphorus as shown by reference oil G.
- the 4-Ball wear performance resulted in 2 to 15 percent improvement in wear reduction or wear scar diameter ("WSD") and 8 to 51 percent improvement in calculated wear volume or K-factor.
- Comparative oils 11 and 12 illustrate the synergists effect of combining borated GMO with borated dispersants.
- Table 11 illustrates the 4-Ball EP and Hot Tube performance of the combination of 0.3 percent ZDDP and 0.3 percent of a non- corrosive sulfur additive for comparative oil 13 versus the 0.6 percent ZDDP reference oil H.
- the total AW/EP additive treat rate is the same 0.6 percent and the EP performance is about the same, but the Hot Tube of Entry 4 is much better indicating a cleaner environment.
- the 4-Ball EP performance of comparative oil 13 is stronger than reference oil I with reduced ZDDP at 0.3% and the base oil in column 3 with 0% ZDDP.
- Table l l l
- a new low SAP engine oil system has been discosvered based on very unique combinations of non-corrosive sulfur additives, low level of ZDDP, borated components, with preferably high level of ashless anti-oxidants.
- This formulation exhibits outstanding and unexpected performance to modern engines.
- One embodiment of this discovery provides an effective way to reduce the amount of ZDDP for contemporary engine oils while maintaining excellent wear, oxidation and corrosion protection.
- This unique component synergism concept is believed to be applicable to similar formulations containing low sulfur base oils of less than 300 ppm, borated additives with borated hydroxy esters such as borated GMO 5 and alternate organic borates such as borated dispersants, non-corrosive sulfur additives, and preferably with ashless antioxidants.
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Abstract
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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JP2009505459A JP5555487B2 (ja) | 2006-04-13 | 2007-04-10 | 非腐食性硫黄および有機ボレートを含む低sapエンジン潤滑油添加剤および組成物 |
EP07775190.7A EP2010636B1 (fr) | 2006-04-13 | 2007-04-10 | Additif et composition lubrifiantes pour moteur à faible taux de soufre, de cendre et de phosphore contenant un composé soufré non corrosif et des borates organiques |
CA002648220A CA2648220A1 (fr) | 2006-04-13 | 2007-04-10 | Additif et composition lubrifiants pour moteur a faible taux de soufre, de cendre et de phosphore contenant du soufre non corrosif et des borates organiques |
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US79177506P | 2006-04-13 | 2006-04-13 | |
US60/791,775 | 2006-04-13 | ||
US11/731,880 US20080171677A1 (en) | 2006-04-13 | 2007-03-30 | Low SAP engine lubricant additive and composition containing non-corrosive sulfur and organic borates |
US11/731,880 | 2007-03-30 |
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WO2007120712A2 true WO2007120712A2 (fr) | 2007-10-25 |
WO2007120712A3 WO2007120712A3 (fr) | 2008-02-21 |
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PCT/US2007/008946 WO2007120712A2 (fr) | 2006-04-13 | 2007-04-10 | Additif et composition lubrifiants pour moteur à faible taux de soufre, de cendre et de phosphore contenant du soufre non corrosif et des borates organiques |
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US (1) | US20080171677A1 (fr) |
EP (1) | EP2010636B1 (fr) |
JP (1) | JP5555487B2 (fr) |
CA (1) | CA2648220A1 (fr) |
WO (1) | WO2007120712A2 (fr) |
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US11788027B2 (en) | 2022-02-18 | 2023-10-17 | Afton Chemical Corporation | Engine oil formulation with improved sequence VIII performance |
Also Published As
Publication number | Publication date |
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WO2007120712A3 (fr) | 2008-02-21 |
JP5555487B2 (ja) | 2014-07-23 |
CA2648220A1 (fr) | 2007-10-25 |
US20080171677A1 (en) | 2008-07-17 |
JP2009533528A (ja) | 2009-09-17 |
EP2010636B1 (fr) | 2015-07-08 |
EP2010636A2 (fr) | 2009-01-07 |
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