US2389527A - Lubricants - Google Patents
Lubricants Download PDFInfo
- Publication number
- US2389527A US2389527A US449177A US44917742A US2389527A US 2389527 A US2389527 A US 2389527A US 449177 A US449177 A US 449177A US 44917742 A US44917742 A US 44917742A US 2389527 A US2389527 A US 2389527A
- Authority
- US
- United States
- Prior art keywords
- oil
- phosphorus
- hydrocarbon
- unsaturated alkyl
- sulfurized
- 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 description 24
- -1 ester radical Chemical class 0.000 description 48
- 239000003921 oil Substances 0.000 description 37
- 229930195733 hydrocarbon Natural products 0.000 description 26
- 150000002430 hydrocarbons Chemical class 0.000 description 26
- 239000004215 Carbon black (E152) Substances 0.000 description 25
- 239000011574 phosphorus Substances 0.000 description 25
- 229910052698 phosphorus Inorganic materials 0.000 description 25
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 24
- 229910052751 metal Inorganic materials 0.000 description 18
- 239000002184 metal Substances 0.000 description 18
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 17
- 239000002253 acid Substances 0.000 description 17
- 239000000203 mixture Substances 0.000 description 16
- 239000011593 sulfur Substances 0.000 description 16
- 229910052717 sulfur Inorganic materials 0.000 description 16
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 14
- 150000003839 salts Chemical class 0.000 description 14
- 239000010687 lubricating oil Substances 0.000 description 12
- 239000000654 additive Substances 0.000 description 10
- 230000003078 antioxidant effect Effects 0.000 description 10
- 230000000996 additive effect Effects 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 238000012360 testing method Methods 0.000 description 8
- 241000208223 Anacardiaceae Species 0.000 description 7
- 241000693997 Anacardium Species 0.000 description 7
- 235000001271 Anacardium Nutrition 0.000 description 7
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000010688 mineral lubricating oil Substances 0.000 description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 229910052788 barium Inorganic materials 0.000 description 4
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- JOLVYUIAMRUBRK-UHFFFAOYSA-N 11',12',14',15'-Tetradehydro(Z,Z-)-3-(8-Pentadecenyl)phenol Natural products OC1=CC=CC(CCCCCCCC=CCC=CCC=C)=C1 JOLVYUIAMRUBRK-UHFFFAOYSA-N 0.000 description 3
- YLKVIMNNMLKUGJ-UHFFFAOYSA-N 3-Delta8-pentadecenylphenol Natural products CCCCCCC=CCCCCCCCC1=CC=CC(O)=C1 YLKVIMNNMLKUGJ-UHFFFAOYSA-N 0.000 description 3
- JOLVYUIAMRUBRK-UTOQUPLUSA-N Cardanol Chemical compound OC1=CC=CC(CCCCCCC\C=C/C\C=C/CC=C)=C1 JOLVYUIAMRUBRK-UTOQUPLUSA-N 0.000 description 3
- FAYVLNWNMNHXGA-UHFFFAOYSA-N Cardanoldiene Natural products CCCC=CCC=CCCCCCCCC1=CC=CC(O)=C1 FAYVLNWNMNHXGA-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- PTFIPECGHSYQNR-UHFFFAOYSA-N cardanol Natural products CCCCCCCCCCCCCCCC1=CC=CC(O)=C1 PTFIPECGHSYQNR-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000006704 dehydrohalogenation reaction Methods 0.000 description 2
- 150000002148 esters Chemical group 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 150000003016 phosphoric acids Chemical class 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 2
- 238000005987 sulfurization reaction Methods 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- RMTXUPIIESNLPW-UHFFFAOYSA-N 1,2-dihydroxy-3-(pentadeca-8,11-dienyl)benzene Natural products CCCC=CCC=CCCCCCCCC1=CC=CC(O)=C1O RMTXUPIIESNLPW-UHFFFAOYSA-N 0.000 description 1
- QARRXYBJLBIVAK-UEMSJJPVSA-N 3-[(8e,11e)-pentadeca-8,11-dienyl]benzene-1,2-diol;3-[(8e,11e)-pentadeca-8,11,14-trienyl]benzene-1,2-diol;3-[(8e,11e,13e)-pentadeca-8,11,13-trienyl]benzene-1,2-diol;3-[(e)-pentadec-8-enyl]benzene-1,2-diol;3-pentadecylbenzene-1,2-diol Chemical compound CCCCCCCCCCCCCCCC1=CC=CC(O)=C1O.CCCCCC\C=C\CCCCCCCC1=CC=CC(O)=C1O.CCC\C=C\C\C=C\CCCCCCCC1=CC=CC(O)=C1O.C\C=C\C=C\C\C=C\CCCCCCCC1=CC=CC(O)=C1O.OC1=CC=CC(CCCCCCC\C=C\C\C=C\CC=C)=C1O QARRXYBJLBIVAK-UEMSJJPVSA-N 0.000 description 1
- IYROWZYPEIMDDN-UHFFFAOYSA-N 3-n-pentadec-8,11,13-trienyl catechol Natural products CC=CC=CCC=CCCCCCCCC1=CC=CC(O)=C1O IYROWZYPEIMDDN-UHFFFAOYSA-N 0.000 description 1
- 244000226021 Anacardium occidentale Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000871335 Semecarpus anacardium Species 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- RDVQTQJAUFDLFA-UHFFFAOYSA-N cadmium Chemical compound [Cd][Cd][Cd][Cd][Cd][Cd][Cd][Cd][Cd] RDVQTQJAUFDLFA-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 235000020226 cashew nut Nutrition 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 208000020442 loss of weight Diseases 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
- 229940031826 phenolate Drugs 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 150000003582 thiophosphoric acids Chemical class 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- DQTMTQZSOJMZSF-UHFFFAOYSA-N urushiol Natural products CCCCCCCCCCCCCCCC1=CC=CC(O)=C1O DQTMTQZSOJMZSF-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- 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
-
- 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
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
-
- 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
- C10N2010/06—Groups 3 or 13
-
- 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
- C10N2010/08—Groups 4 or 14
-
- 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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/14—Group 7
-
- 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
- C10N2010/16—Groups 8, 9, or 10
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/135—Steam engines or turbines
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/46—Textile oils
-
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
Definitions
- This invention relates to an improved lubricant, and particularly to a compounded lubricant containing an oil-soluble metal derivative of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a suliurized alkyi phenol.
- the improved lubricants to which the present invention is directed are those lubricants which are normally subject to oxidation and corrosion tendencies during service and include the petroleum lubricating oils for internal combustion engines such as Diesel oils, motor oils, heavy duty oils and aviation oils, together with the compounding lubricants such as are used in textile oils, greases and industrial lubricants.
- the term-sulfur-containing substituted acid of phosphorus is used to denote the acidic radical or radicals obtained by reacting a sulfide of phosphorus with a phenol or metal phenolate.
- the arrangement of the sulfur, oxygen, and phosphorus atoms in the radicals apparently depends upon the conditions of reaction and probably results in a mixture of different types of sulfur-containing acids of phosphorus in the final composition.
- the particular sulfide of phosphorus used in the preparation of the additive composition depends upon whether a thio derivative of phosphoric or phosphorous acid is preferred.
- phosphorus pentasulfide In the present instance the thin-derivatives of phosphoric acid are preferred and for that reason phosphorus pentasulfide will be used in the description of the invention. This is not to be construed as limiting the invention to the use of phosphorus pentasulfide or the thiophosphoric acids resulting therefrom but merely as an example of a sulfide of phosphorus and one method of preparing the sulfur-containing acids of phosphorus.
- the ester substituent of the additive composition is derived from a sulfurized alkyl phenol and is linked to the sulfur-containing acid of phosphorus through the, hydroxyl group.
- the unsaturated alkyl phenol may be either a monoor polyhydric phenol and may contain one or more unsaturated alkyl substituents attached to the nucleus. Included within this category are the unsaturated alkyl phenols which contain further substituents attached to the nucleus in the form of aliphatic or aromatic substituents.
- oilsolubility depends on the number of aliphatic carbon atoms attached to the nucleus of the phenols and for the purposes of the present invention the aliphatic carbon atoms should exceed five in number.
- the unsaturated alkyl phenols are selected from the phenolic'compositions obtained or derived from the Anacardium genus of the Anacardiaceae family which includes such unsaturated alhyl phenols as cardanol (CzoHazO), anacardol (018E300) and urushiol (CzoHanOa).
- These phenolic coinpositions are usually monoor dihydric phenols containing long-chain unsaturated alhyl radi cals attached to the nucleus and are either pre sent in the oils such as cashew nut shell oil, marking nut shell 011, Japanese lac, etc, or are formed by the decomposition of other aromatic compounds contained therein.
- the metal salts of the invention may consist of any of the metals found in groups I, II, III, IV, VI, VH, and VIII of the period table. of elements and includes such metals as sodium, potassium, lithium, calcium, barium, strontium, tin, bismuth, aluminum, zinc, magnesium,'cadmium, lead, titanium, antimony, chrominum, manganese, cobalt, nickel, iron and copper with preference givento the alkaline earth metals and tin and zinc.
- the amount of additive incorporated in the oil is dependent upon the type of lubricant and the degree of improvement desired. In the majority of instances, the proportion of additive compounded with the oil will not exceed 5% and will vary from 0.01-5%.
- compositions of the present invention whenincorporated in a hydrocarbonllubricating oil, has been demonstrated by.
- Example I To 285 grams of partially hydrogenated cardahol (bromine number 64-65) were added 315 grams of 300 pale oil and 28'grams of elemental sulfur. The mass was heated to 150l60 C. and the sulfurization reaction .was conducted for six hours. were added 50 grams of barium hydroxide and 300 cc. of toluene. The mixture was heated on a pressure steam bath and refluxed until no more water was removed after which the product was filtered.
- a lubricant comprising a hydrocarbon lubri-' eating oil having incorporated therein 0.01-5.0%
- a lubricant comprising a hydrocarbon lubricating oil having incorporated therein 0.01-5.0% by weight of an oil-miscible metal salt of a sulfurcontaining substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized phenolic composition obtained from the Anacardium' genus of the Anacardiaceae family.
- a lubricant comprising a hydrocarbon oil and 0.0l5.0% by weight of an oil-miscible alkaline earth metal salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized phenolic composition obtained from the Anacardium genus 4.
- a lubricant comprising a hydrocarbon oil and 0.01-5.0% by weight of an oil-miscible tin salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized unsaturated alkyl phenol containing at least five carbon atoms in the unsaturated alkyl radical thereof.
- a lubricant comprising a hydrocarbon oil and 0.01-5.0% by weight of an oil-miscible tin salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized phenolic composition obtained from the Anacardium genus of the Anacardiaceae family.
- a lubricant comprising a hydrocarbon oil and an amount, suflicient to impart anti-oxidant properties to said hydrocarbon oil, of an oil-miscible metal salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized unsaturated alkyl phenol containing at least five carbon atoms in the unsaturated alkyl radical thereof.
- a lubricant comprising a mineral lubricating oil and an amount, sufiicient to impart anti-oxidant properties to said mineral lubricating oil, of an oil-miscible metal salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized unsaturated alkyl phenol containing at least five carbon atoms in the unsaturated alkyl radical thereof.
- a lubricant comprising a hydrocarbon oil and an amount, sufiicient to impart anti-oxidant properties to said hydrocarbon oil, of an oil-miscible metal salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized phenolic composition obtained from the Anacardium genus of the Anacardiaceae family.
- a lubricant comprising a mineral lubricating oil and an amount, sumcient to impart anti-oxidant properties to said mineral lubricating oil, of an oil-miscible metal salt of a sulfur-con substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized phenolic composition obtained from the Anacardium genus of the Anacardiaceae family.
- a lubricant comprising a hydrocarbon lubricating oil and an amount. suflicient to impart anti-oxidant properties to said hydrocarbon lubricating oil, of an oil-soluble metal salt of the acidic reaction product obtained by reacting a sulfide of phosphorus with a suifurlzed unsaturated alhl phenol containing at least flve carbon atoms in the unsaturated alkyl radical thereof.
- a lubricant comprising a hydrocarbon lubricating oil and an amount, suilicient to impmt anti-oxidant propertiesto said hydrocarbon lubricating oil, of an oil-soluble metal salt of the acidic reaction product obtained by reacting a sulfide of phosphorus with a sulfurized phenolic composition derived from the Anacardium genus of the Anacardiaceae family.
- a lubricant comprising a hydrocarbon lubricating oil and an amount, sufficient to impart anti-oxidant properties to said hydrocarbon lubricating oil, of an oil-soluble reaction product obtained by reacting a sulfide of phosphorus with a metal salt of a sulfurized unsaturated al yl phenol containing at least flve carbon atoms in the unsaturated alkyl radical thereof.
- a lubricant comprising a hydrocarbon oil and an amount, sufficient toimpart anti-oxidant properties to said hydrocarbon oil, of an oil-soluble metal salt of a sulfur-containing substituted phosphoric acid possessing at least one ester radical derived from a sulfm'ized unsaturated alkyl phenol containing at least five carbon atoms in the unsaturated alkyl radical thereof.
- a lubricant comprising a hydrocarbon oil and an amount, suflicient to impart anti-oxidant properties to said hydrocarbon oil, of an oil-soluble metal salt of the acidic reaction product obtained by reacting phosphorus pentasulflde with a sulfurized unsaturated alkyl phenol containing at least five carbon atoms in the unsaturated alkyl radical thereof.
- a lubricant comprising a hydrocarbon oil and an amount, suflicient to impart anti-oxidant properties to said hydrocarbon oil.
- suflicient to impart anti-oxidant properties to said hydrocarbon oil.
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- Chemical & Material Sciences (AREA)
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- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Nov. 20, 1945 LUBRICAN T S Rush F. McClcary, Beacon, N. 1., assignor to The Texas Company, New York, N. lit, a corporation of Delaware No Drawing. Application June 30, 1942, SerialNo. M9927? 15 Claims.
This invention relates to an improved lubricant, and particularly to a compounded lubricant containing an oil-soluble metal derivative of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a suliurized alkyi phenol.
The improved lubricants to which the present invention is directed are those lubricants which are normally subject to oxidation and corrosion tendencies during service and include the petroleum lubricating oils for internal combustion engines such as Diesel oils, motor oils, heavy duty oils and aviation oils, together with the compounding lubricants such as are used in textile oils, greases and industrial lubricants.
It has been discovered that when small amounts of an oil-soluble or oil-miscible metal salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurlzed alkyl phenol are incorporated in a hydrocarbon lubricating oil, the resulting oil, together with lubricants compounded therewith, are rendered substantially resistant to oxidation and corrosion under operating conditions.
Although the principal function of this type of additive ingredient in a lubricating oil is the inhibition of oxidation and corrosion, other advantageous features result which enhance their value as improving agents. It has been found 7 that besides the foregoing properties mentioned these additives increase the load-carrying or extreme pressure qualities of the oil and act as a dispersing agent for undissolved carbonaceous materials.
In defining the additive ingredients of the present invention, the term-sulfur-containing substituted acid of phosphorus is used to denote the acidic radical or radicals obtained by reacting a sulfide of phosphorus with a phenol or metal phenolate. The arrangement of the sulfur, oxygen, and phosphorus atoms in the radicals apparently depends upon the conditions of reaction and probably results in a mixture of different types of sulfur-containing acids of phosphorus in the final composition. The particular sulfide of phosphorus used in the preparation of the additive composition depends upon whether a thio derivative of phosphoric or phosphorous acid is preferred. In the present instance the thin-derivatives of phosphoric acid are preferred and for that reason phosphorus pentasulfide will be used in the description of the invention. This is not to be construed as limiting the invention to the use of phosphorus pentasulfide or the thiophosphoric acids resulting therefrom but merely as an example of a sulfide of phosphorus and one method of preparing the sulfur-containing acids of phosphorus.
The ester substituent of the additive composition is derived from a sulfurized alkyl phenol and is linked to the sulfur-containing acid of phosphorus through the, hydroxyl group. These sul= furized alkyl phenols are obtained by the sulfurization of unsaturated alkyl phenols containing one or more double bonds in the alkyl radical. The unsaturated alkyl phenol may be either a monoor polyhydric phenol and may contain one or more unsaturated alkyl substituents attached to the nucleus. Included within this category are the unsaturated alkyl phenols which contain further substituents attached to the nucleus in the form of aliphatic or aromatic substituents. It has been found desirable to start the chain of reactions with an unsaturated alkyl phenol which is oil-soluble since the ester substituent is usually the determining factor in the oil-solubility of the final composition. The oilsolubility depends on the number of aliphatic carbon atoms attached to the nucleus of the phenols and for the purposes of the present invention the aliphatic carbon atoms should exceed five in number.
In the preferred form of the invention, the unsaturated alkyl phenols are selected from the phenolic'compositions obtained or derived from the Anacardium genus of the Anacardiaceae family which includes such unsaturated alhyl phenols as cardanol (CzoHazO), anacardol (018E300) and urushiol (CzoHanOa). These phenolic coinpositions are usually monoor dihydric phenols containing long-chain unsaturated alhyl radi cals attached to the nucleus and are either pre sent in the oils such as cashew nut shell oil, marking nut shell 011, Japanese lac, etc, or are formed by the decomposition of other aromatic compounds contained therein.
The invention is not restricted to this source of unsaturated alkyl phenols and includes such unsaturated compounds as may be prepared by chlorination of high molecular weight hydrocarbons followed by condensation with a phenol and subsequent dehydrohalogenation of the chlorine atoms remaining in the alkyl radical or by chlo= rination of a poly substituted alkyl phenol followed by dehydrohalogenation.
These methods of preparing the unsaturated alkyl phenols are only an illustration of the various method of preparation and may be modified or changed in accordance with the desired prodnot.
When sulfurizing the unsaturated alkyl radicals, it is preferable to sulfurize with elemental sulfur at comparatively low'temperatures, e. g., below 200 C. in the'presence of a hydrocarbon solvent. It has been found that reactions carried out at higher temperatures tend to promote polymerization of thephenol and result in oil-insoluble sulfurized products. Another suitable method for preventing polymerization inthe highly unsaturated phenols is to partially hydrogenat the unsaturated alkyl radical and thereby stabilize the more reactive double bonds.
The metal salts of the invention may consist of any of the metals found in groups I, II, III, IV, VI, VH, and VIII of the period table. of elements and includes such metals as sodium, potassium, lithium, calcium, barium, strontium, tin, bismuth, aluminum, zinc, magnesium,'cadmium, lead, titanium, antimony, chrominum, manganese, cobalt, nickel, iron and copper with preference givento the alkaline earth metals and tin and zinc.
In compounding the additive ingredient in a hydrocarbon lubricating oil, the amount of additive incorporated in the oil is dependent upon the type of lubricant and the degree of improvement desired. In the majority of instances, the proportion of additive compounded with the oil will not exceed 5% and will vary from 0.01-5%.
The effectiveness of the compositions of the present invention, whenincorporated in a hydrocarbonllubricating oil, has been demonstrated by.
empirical tests which were designed to simulate actual operating conditions in automotive engines.- The following empirical test was designed oil was heated to a controlled temperature of 350 F. and continuously circulated between the bear-' ing specimen and the shaft for a period'ofhours. uouslyagitated by copper 'ballles which acted as oxidation accelerators. The bearing specimen was weighed before the test and after the 10- hour period and the loss of weight recorded in milligrams. The reference oil used in this test was a solvent-refined, dewaxed, Mid-Continent lubricating oil of an S. A. E. v grade. The results of.=the reference oil were then used as a comparison against the reference oil compounded with the composition prepared in the foregoing For simplicity, the composition presulfurized cardanyl thio-phosphate.
The preferred range of proportions in a mineral lubricating oil when used in a few of the more common services are as follows:
Per cent by weight of The following example illustrates one of the various methods of preparing the metal salts of sulfurcontaining substituted acids of-phosphorus possessing at least one ester radical derived from a sulfurized alkyl phenol:
Example I To 285 grams of partially hydrogenated cardahol (bromine number 64-65) were added 315 grams of 300 pale oil and 28'grams of elemental sulfur. The mass was heated to 150l60 C. and the sulfurization reaction .was conducted for six hours. were added 50 grams of barium hydroxide and 300 cc. of toluene. The mixture was heated on a pressure steam bath and refluxed until no more water was removed after which the product was filtered.
To the resulting barium salt of sulfurized cardanol was added 45 grams of phosphorus pentasulfide and the reaction mixture heated on the steam bath for 12 hours. This product was then cooled, filtered and stripped of the solvent. The resulting reaction product analyzed as follows:
To 314 grams of the sulfurized cardanol Per cent Barium 7.8 Phosphorus 2.5 Sulfur BEARING CORROSIONCOPPERLE AD (10 Hotms) Loss of weightmgs.
350 F. Reference oil 162-139 Reference oil+l.0% of barium sulfurized cardanyl thio'phosphate Z 4-3 An additional test was carried out on a conventional Almen testing machine to demonstrate the improvement in load-carrying or extreme This Throughout the test the oil was continf pressure properties produced by the incorporation of the aforementioned additive ingredients. same reference oil and compounded oil which was used for the bearing corrosiontest was used in the present Almen test. The results obtained are as follows:
' ALMEN Tssr A Load in lbs. Reference oil 5.3 Reference oil+l.0% of barium sulfurized cardanyl thiophosphate 21.6+
The hydrocarbon oilsto which the additive inmade without departing from the spirit and scope thereof and, therefore, only such limitations should be imposed as are indicated in the appended claims.
I claim:
1. A lubricant comprising a hydrocarbon lubri-' eating oil having incorporated therein 0.01-5.0%
by weight of an oil-miscible metal salt of a sulfurcontaining substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized unsaturated alkyl phenol containing at 'of the'Anacardiaceae family. 7
least flve carbon atoms in the unsaturated alkyl radical thereof.
2. A lubricant comprising a hydrocarbon lubricating oil having incorporated therein 0.01-5.0% by weight of an oil-miscible metal salt of a sulfurcontaining substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized phenolic composition obtained from the Anacardium' genus of the Anacardiaceae family.
3. A lubricant comprising a hydrocarbon oil and 0.0l5.0% by weight of an oil-miscible alkaline earth metal salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized phenolic composition obtained from the Anacardium genus 4. A lubricant comprising a hydrocarbon oil and 0.01-5.0% by weight of an oil-miscible tin salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized unsaturated alkyl phenol containing at least five carbon atoms in the unsaturated alkyl radical thereof.
5. A lubricant comprising a hydrocarbon oil and 0.01-5.0% by weight of an oil-miscible tin salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized phenolic composition obtained from the Anacardium genus of the Anacardiaceae family.
6. A lubricant comprising a hydrocarbon oil and an amount, suflicient to impart anti-oxidant properties to said hydrocarbon oil, of an oil-miscible metal salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized unsaturated alkyl phenol containing at least five carbon atoms in the unsaturated alkyl radical thereof.
'7. A lubricant comprising a mineral lubricating oil and an amount, sufiicient to impart anti-oxidant properties to said mineral lubricating oil, of an oil-miscible metal salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized unsaturated alkyl phenol containing at least five carbon atoms in the unsaturated alkyl radical thereof.
8. A lubricant comprising a hydrocarbon oil and an amount, sufiicient to impart anti-oxidant properties to said hydrocarbon oil, of an oil-miscible metal salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized phenolic composition obtained from the Anacardium genus of the Anacardiaceae family.
9. A lubricant comprising a mineral lubricating oil and an amount, sumcient to impart anti-oxidant properties to said mineral lubricating oil, of an oil-miscible metal salt of a sulfur-con substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized phenolic composition obtained from the Anacardium genus of the Anacardiaceae family.
10. A lubricant comprising a hydrocarbon lubricating oil and an amount. suflicient to impart anti-oxidant properties to said hydrocarbon lubricating oil, of an oil-soluble metal salt of the acidic reaction product obtained by reacting a sulfide of phosphorus with a suifurlzed unsaturated alhl phenol containing at least flve carbon atoms in the unsaturated alkyl radical thereof.
11. A lubricant comprising a hydrocarbon lubricating oil and an amount, suilicient to impmt anti-oxidant propertiesto said hydrocarbon lubricating oil, of an oil-soluble metal salt of the acidic reaction product obtained by reacting a sulfide of phosphorus with a sulfurized phenolic composition derived from the Anacardium genus of the Anacardiaceae family.
12. A lubricant comprising a hydrocarbon lubricating oil and an amount, sufficient to impart anti-oxidant properties to said hydrocarbon lubricating oil, of an oil-soluble reaction product obtained by reacting a sulfide of phosphorus with a metal salt of a sulfurized unsaturated al yl phenol containing at least flve carbon atoms in the unsaturated alkyl radical thereof.
13. A lubricant comprising a hydrocarbon oil and an amount, sufficient toimpart anti-oxidant properties to said hydrocarbon oil, of an oil-soluble metal salt of a sulfur-containing substituted phosphoric acid possessing at least one ester radical derived from a sulfm'ized unsaturated alkyl phenol containing at least five carbon atoms in the unsaturated alkyl radical thereof.
14. A lubricant comprising a hydrocarbon oil and an amount, suflicient to impart anti-oxidant properties to said hydrocarbon oil, of an oil-soluble metal salt of the acidic reaction product obtained by reacting phosphorus pentasulflde with a sulfurized unsaturated alkyl phenol containing at least five carbon atoms in the unsaturated alkyl radical thereof.
15. A lubricant comprising a hydrocarbon oil and an amount, suflicient to impart anti-oxidant properties to said hydrocarbon oil. of an oil-m1scible alkaline earth metal salt of a sulfur-containing substituted acid of phosphorus possessing at least one ester radical derived from a sulfurized alkyl phenol containing at least flve carbon atoms in the unsaturated alkyl radical thereof.
Rusrr F. MccLEARY.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US449177A US2389527A (en) | 1942-06-30 | 1942-06-30 | Lubricants |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US449177A US2389527A (en) | 1942-06-30 | 1942-06-30 | Lubricants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2389527A true US2389527A (en) | 1945-11-20 |
Family
ID=23783184
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US449177A Expired - Lifetime US2389527A (en) | 1942-06-30 | 1942-06-30 | Lubricants |
Country Status (1)
| Country | Link |
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| US (1) | US2389527A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2417562A (en) * | 1942-07-15 | 1947-03-18 | Texas Co | Lubricant |
| US2475143A (en) * | 1945-12-19 | 1949-07-05 | Texas Co | Phosphoric acid ester of hydrogenated sulfurized cardanol |
| US2497132A (en) * | 1947-03-14 | 1950-02-14 | Standard Oil Dev Co | Lubricating oil composition |
| US2530339A (en) * | 1946-12-24 | 1950-11-14 | Standard Oil Dev Co | Compounded petroleum hydrocarbon products |
| US2552570A (en) * | 1947-11-28 | 1951-05-15 | Standard Oil Dev Co | Oxidation resisting hydrocarbon products |
| US5102566A (en) * | 1987-10-02 | 1992-04-07 | Exxon Chemical Patents Inc. | Low ash lubricant compositions for internal combustion engines (pt-727) |
| US5141657A (en) * | 1987-10-02 | 1992-08-25 | Exxon Chemical Patents Inc. | Lubricant compositions for internal combustion engines |
| US5320765A (en) * | 1987-10-02 | 1994-06-14 | Exxon Chemical Patents Inc. | Low ash lubricant compositions for internal combustion engines |
-
1942
- 1942-06-30 US US449177A patent/US2389527A/en not_active Expired - Lifetime
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2417562A (en) * | 1942-07-15 | 1947-03-18 | Texas Co | Lubricant |
| US2475143A (en) * | 1945-12-19 | 1949-07-05 | Texas Co | Phosphoric acid ester of hydrogenated sulfurized cardanol |
| US2530339A (en) * | 1946-12-24 | 1950-11-14 | Standard Oil Dev Co | Compounded petroleum hydrocarbon products |
| US2497132A (en) * | 1947-03-14 | 1950-02-14 | Standard Oil Dev Co | Lubricating oil composition |
| US2552570A (en) * | 1947-11-28 | 1951-05-15 | Standard Oil Dev Co | Oxidation resisting hydrocarbon products |
| US5102566A (en) * | 1987-10-02 | 1992-04-07 | Exxon Chemical Patents Inc. | Low ash lubricant compositions for internal combustion engines (pt-727) |
| US5141657A (en) * | 1987-10-02 | 1992-08-25 | Exxon Chemical Patents Inc. | Lubricant compositions for internal combustion engines |
| US5320765A (en) * | 1987-10-02 | 1994-06-14 | Exxon Chemical Patents Inc. | Low ash lubricant compositions for internal combustion engines |
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