US2221162A - Lubricating oil - Google Patents
Lubricating oil Download PDFInfo
- Publication number
- US2221162A US2221162A US223527A US22352738A US2221162A US 2221162 A US2221162 A US 2221162A US 223527 A US223527 A US 223527A US 22352738 A US22352738 A US 22352738A US 2221162 A US2221162 A US 2221162A
- Authority
- US
- United States
- Prior art keywords
- oil
- phosphatide
- emulsion
- bearings
- motor
- 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
- 239000010687 lubricating oil Substances 0.000 title description 8
- 239000010705 motor oil Substances 0.000 description 38
- 239000003921 oil Substances 0.000 description 38
- 235000019198 oils Nutrition 0.000 description 38
- 239000000839 emulsion Substances 0.000 description 33
- 239000003795 chemical substances by application Substances 0.000 description 21
- 150000001875 compounds Chemical class 0.000 description 16
- 238000005260 corrosion Methods 0.000 description 16
- 230000007797 corrosion Effects 0.000 description 16
- 239000004922 lacquer Substances 0.000 description 14
- 239000000787 lecithin Substances 0.000 description 14
- 235000010445 lecithin Nutrition 0.000 description 14
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 13
- 230000015572 biosynthetic process Effects 0.000 description 13
- 238000002485 combustion reaction Methods 0.000 description 13
- 229940067606 lecithin Drugs 0.000 description 13
- 230000001050 lubricating effect Effects 0.000 description 13
- 239000010688 mineral lubricating oil Substances 0.000 description 13
- 239000000344 soap Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 12
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 10
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 8
- 229940083466 soybean lecithin Drugs 0.000 description 8
- 239000003513 alkali Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 125000005609 naphthenate group Chemical group 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- CFWRDBDJAOHXSH-SECBINFHSA-N 2-azaniumylethyl [(2r)-2,3-diacetyloxypropyl] phosphate Chemical compound CC(=O)OC[C@@H](OC(C)=O)COP(O)(=O)OCCN CFWRDBDJAOHXSH-SECBINFHSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 150000001342 alkaline earth metals Chemical class 0.000 description 5
- 230000002401 inhibitory effect Effects 0.000 description 5
- KQSJSRIUULBTSE-UHFFFAOYSA-M sodium;3-(3-ethylcyclopentyl)propanoate Chemical compound [Na+].CCC1CCC(CCC([O-])=O)C1 KQSJSRIUULBTSE-UHFFFAOYSA-M 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 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 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 150000001414 amino alcohols Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- NSAODVHAXBZWGW-UHFFFAOYSA-N cadmium silver Chemical compound [Ag].[Cd] NSAODVHAXBZWGW-UHFFFAOYSA-N 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical group 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000002195 soluble material Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical group CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000005608 naphthenic acid group Chemical group 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- ZVUVJTQITHFYHV-UHFFFAOYSA-M potassium;naphthalene-1-carboxylate Chemical group [K+].C1=CC=C2C(C(=O)[O-])=CC=CC2=C1 ZVUVJTQITHFYHV-UHFFFAOYSA-M 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- C10M141/10—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/16—Naphthenic acids
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/062—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups bound to the aromatic ring
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/26—Amines
-
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
-
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/086—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing sulfur atoms bound to carbon atoms of six-membered aromatic rings
-
- 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
- C10M2223/10—Phosphatides, e.g. lecithin, cephalin
-
- 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
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
Definitions
- X in the case of lecithin, X, or the amino alcohol group, is ch0lineCI-I2CHzN(CH3)aOH; and in the case of cephalin X is colamine-CHzCHnNHz.
- Other types of compounds falling within the class of phosphatides can be employed such as sphengomyelin.
- metal derivatives or salts of the leclthins can be employed.
- the free acid group of the compound can be neutralized with alkali, alkaline earth and other bases to form the corresponding salts thereof.
- a preferred composition for this purpose is commercial soybean lecithin, such as the product known commercially as LipoidoP which consists essentially of about equal proportions of lecithin and cephalin with a smaller proportion of soybean oil.
- a bleached commercial soybean lecithin such as the product sold commercially as Coloidol BT" which is commercial soybean lecithin bleached with hydrogen peroxide and dibenzoyl peroxide, or the product sold commercially as Coloidol HX which is commercial soybean lecithin bleached with hydrogen peroxide.
- the commercial soybean lecithin can be purified by extracting the soybean oil with acetone to obtain a product consisting essentially of lecithin and cephalin, which is also suitable for the purposes of the present invention.
- the cephalin constituent can be separated from the lecithin by alcohol extraction, and either the purified lecithin or purified cephalin or mixtures of the two in any desired proportion may be employed for purposes of the present invention.
- the purified constituents do not display any marked improvement over the bleached commercial soybean lecithin, and the latter is generally preferred for economical reasons.
- phosphatide compound is used throughout the description and claims, it is to be understood that this includes any of the purified compounds falling within this group as well as any of the comparatively impure mixtures such as the commercial grades mentioned above.
- the phosphatide compound is added to the motor oil in a critical proportion range of about 0.01-2.0%. It is found that these percentages are critical in securing the desired improvement with respect to inhibiting bearing corrosion and lacquer formation and without affecting other desirable properties of the oil, while proportions above this range produce undue sludging. In the case of motor oils adapted for automotive use, a range of 0.01 to 0.25% appears most satisfactory, with about 0.1% preferred. Somewhat higher percentages may be employed in Diesel lubricating oil or airplane oil where it is desired to improve materially the ring sticking properties of the oil in addition to obtaining the benefits of inhibiting bearing corrosion and lacquer formation.
- a very satisfactory method for adding the phosphatide compound to the mineral lubricating oil is to first form a concentrate, such as a solution of the lecithin or other phosphatide compound in a S. A. E. 30 oil or other lubricating 011 within the motor oil viscosity range, and then add the concentrate to the mineral lubricating oil in an amount suflicient to give the desired percenta'g of phosphatide compound therein.
- a concentrate such as a solution of the lecithin or other phosphatide compound in a S. A. E. 30 oil or other lubricating 011 within the motor oil viscosity range
- the phosphatide additive is particularly efl'ective in connection with highly solvent refined lubricat- 'varnish or lacquer formation.
- This lacquer generally appears as a yellowish or reddish brown film which deposits upon the metal surfaces, piston rings and cylinder walls during operation of the engine over extended periods of time.
- this problem is so severe as to frequently result in seizure of the pistons when the motor is stopped and allowed to cool.
- the phosphatide compound is unique in combining in one substance the properties of inhibiting or minimizing this objectionable lacquer formation and of also inhibiting bearing corrosion, reducing cylinder and piston wear, reducing oil ring and compression groove deposits and improving ring sticking of the motor oil to which the compound is added in the small proportion range specified above.
- the quaternary organic ammonium soaps ofthe general formula in which R, R, R", R' represent the same or different alkyl, aralkyl or aryl groups or combinations thereof, and in which x is a fatty acid or naphthenic acid radical, are also highly effective for this purpose.
- compounds formed by substituting one or more of the hydrogens of the alkyl, aralkyl or aryl groups of such quaternary organic ammonium soaps with halogen, oxygen or sulfur, are also included.
- tetrone B naphthenate which is a quaternary ammonium soap and is believed to be trimethyl phenyl ammonium naphthenate (CaHs) (CHa)aN-naphthenate.
- CaHs trimethyl phenyl ammonium naphthenate
- emulsion preventing agent is preferably used in the range of 0.02-0.5%.
- a very satisfactory motor oil for automotive purposes is obtained by adding about 0.1% of a phosphatide, and about 0.10.2% of an emulsion preventing agent of the character of sodium naphthenate or tetrone B naphthenate.
- a light lubricating oil having a Saybolt viscosity of less than seconds at 100 F. to produce a textile fiber spraying oil (see U. S. Patent No. 2,002,885).
- the lecithin was employed here to improve the wetting or filming of the oil for the textile fibres and the soap was employed to assist in washing off the 011 after the fibres had been processed.
- the present invention is distinguished in the addition of lecithin to a different type of lubricating oil (a motor oil adapted for lubricating the bearings and cylinders of an internal combustion engine) which is of a different viscosity range as falling within the motor oil viscosity range and having a Saybolt viscosity in excess of 100 at 100 F.
- a motor oil viscosity range it is understood that this embraces the motor oils falling within the S. A. E. 10 to 60 grades as well as certain heavier motor oils adapted for special use in heavy duty truck or bus engines, at higher atmospheric temperatures and having a viscosity range varying from about 90 seconds at F. up to about seconds at 210 F. Saybolt Universal, as shown on page 444 of the 1936 edition of the S. A. E. Handbook.
- the present invention is further distinguished in that the lecithin is employed for an entirely different purpose of inhibiting lacquer formation and bearing corrosion, which are entirely new and unexpected properties unrelated to the fibre wetting or filming action of the prior art.
- the present invention is further distinguished in the use of a different and critical proportion range of "sodium naphthenate or other emulsion preventing agent for the different purpose of improving the emulsion test of the motor oil, which is remote from the detergent action of the soap of the prior art.
- i'Reierence oil was furiural refined dewaxed Mid-Continent distiliajtgflSAE. 20 grade.
- the oil was circulated between the bushing and its journal by a suitable propeller or "whirligig" for a period of five hours.
- the bushing was removed from the pot at intervals of five hours, weighed and returned. The loss in weight is expressed in milligrams and is considered the corrosion loss.
- the reference oil employed was furfural refined dewaxed Mid-Continent lubricating oil of S. A. E. 30 grade.
- these phosphatide compounds and particularly the purified compounds or the bleached soybean lecithin, and the emulsion preventing agents, such as the naphthenates prepared from purified naphthenic acids, can be added to high grade typical motor oils without objectionably aifecting desirable properties or tests of these oils as illustrated in the followin table:
- Reference Reference oil plus oil additives Material A, added Coloidol BT. Material A- ercent Material B, added sodutgn naphthena Material B .-peroent 0.1 Gravity A P I 28. 2 Flash. 0 475 Fire, 0. 0 540 Viscosity, 1 526-528 Viscosity, 63-63 Color Lovlbond 6"- 300 Pour F -5 0 Carbon residue percent 0. 09-0. 10 0. 13-0. 11 Neut. N um r 0. 01 m. Number 0. 7-0. 6 mrmnt ,0]
- a motor oil for lubricating the bearings and cylinders of an internal combustion engine comprising a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about at F. to about at 210 F., containing about 0.01-2.0% of a phosphatide to inhibit bearing corrosion and lacquer formation and less than 1% of an emulsion preventing agent capable of improving the emulsion test of the oil in the presence of the phosphatide.
- a motor oil for lubricating the bearings and cylinders of an internal combustion engine comprising a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about at F, to about at 210 F., containing about 0.012.0% of a lecithin, and about 0.02-0.9% of an emulsion preventing agent capable of improving the emulsion test of the oil in the presence of the lecithin.
- a motor oil for lubricating the bearings and cylinders of an internal combustion engines comprising a highly solvent refined mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 containing about 0.01-0.257. of a phosphatide and about 0.02-0.5% of an emulsion preventing agent which is oil soluble and which hydrolyzes in the presence of water to give an alkaline reaction.
- a motor oil for lubricating bearings and cylinders of an internal combustion engine comprising a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing about 0.1% of a phosphatide and about 0.l-0.2% of an oil soluble soap of an alkali or alkaline earth metal which acts as an agent capable of improving the emulsion test of the oil in the presence of the phosphatide.
- a motor oil for lubricating bearings and cylinders of an internal combustion engine comprising a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing about 0.1% of a bleached commercial soybean lecithin and about 0.1% of sodium naphthenate'.
- the method of lubricating bearings and cylinders of an internal combustion engine which comprises supplying to the bearings and cylinders of said engine a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing a small proportion of a phosphatide of the order of about 0.01-2.0% suillcient to inhibit bearing corrosion and lacquer formation, and containing less than about 1% of an agent capable of improving the emulsion test of the oil in the presence of the phosphatide.
- the method of lubricating bearings and cylinders of an internal combustion engine which comprises supplying to the bearings and cylinders of said engine a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing less than about 1% of a phosphatide and containing less than about 1% of an oil soluble soap of an alkali or alkaline earth metal capable of improving the emulsion test of the oil in the presence of the phosphatide.
- the method of lubricating the bearings and cylinders in an internal combustion engine which comprises supplying to the bearings and cylinders of said engine a highly solvent refined mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing about 0.010.25% of a phosphatide to inhibit bearing corrosion and lacquer formation, and about 0.02-0.5% of an agent capable of improving the emulsion test of the oil in the presence of the phosphatide.
- the method of lubricating the bearings and cylinders in an internal combustion engine which comprises supplying to the bearings and cylinders of said engine a highly solvent refined mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing about 0.1% of a phosphatide to inhibit bearing corrosion and lacquer formation and about 0.0l0.2% of an oil soluble soap of an alkali or alkaline earth metal capable of improving the emulsion test of the oil in the presence of the phosphatide.
- the method of lubricating the bearings, cylinders and pistons of an internal combustion engine which comprises supplying to the bearings, cylinders and pistons of said engine a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F.
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Description
Boh -ED. "STATES even date herewith, there is disclosed and claimed Patented Nov. 12, 1940 PATENT. OFFICE LUBRICA'I'ING OIL Harry V. Ashburn, Gienham, and William G. Aisop, Fishkill, N. Y., assignors to The Texas Compm, New York, N. Y., a corporation of Dela- This invention relates to a lubricating oil, and particularly to a motor oil adapted for lubrication of the bearings and cylinders of internal combustion engines, such as automotive engines, airplane engines, Diesel engines and the like.
In the co-pending application of Frank W. Hall and CharlesC. Towne Serial No. 223,487 filed of the addition to a motor oil of this type of a small proportion of a phosphatide or phospholipine, such as lecithin, to reduce or inhibit bearing corrosion and lacquer formation while affording other advantages as set forth more fully therein. The phosphatides, orthe lecithins as they are frequently called, belong to the class of compounds having the general formula CHaOR now on mo-r=o where R and R. are similar or dissimilar fatty acyl radicals derived from stearic, palmitic, oleic acid, etc., and whereXrepresents an amino alcohol group. In the case of lecithin, X, or the amino alcohol group, is ch0lineCI-I2CHzN(CH3)aOH; and in the case of cephalin X is colamine-CHzCHnNHz. Other types of compounds falling within the class of phosphatides can be employed such as sphengomyelin. Also metal derivatives or salts of the leclthins can be employed. For example, the free acid group of the compound can be neutralized with alkali, alkaline earth and other bases to form the corresponding salts thereof.
A preferred composition for this purpose is commercial soybean lecithin, such as the product known commercially as LipoidoP which consists essentially of about equal proportions of lecithin and cephalin with a smaller proportion of soybean oil. In some cases it is found preferable to employ a bleached commercial soybean lecithin, such as the product sold commercially as Coloidol BT" which is commercial soybean lecithin bleached with hydrogen peroxide and dibenzoyl peroxide, or the product sold commercially as Coloidol HX which is commercial soybean lecithin bleached with hydrogen peroxide. If desired, the commercial soybean lecithin can be purified by extracting the soybean oil with acetone to obtain a product consisting essentially of lecithin and cephalin, which is also suitable for the purposes of the present invention. Also,- the cephalin constituent can be separated from the lecithin by alcohol extraction, and either the purified lecithin or purified cephalin or mixtures of the two in any desired proportion may be employed for purposes of the present invention. However, it has been found that the purified constituents do not display any marked improvement over the bleached commercial soybean lecithin, and the latter is generally preferred for economical reasons.
Wherever the expression phosphatide compound" is used throughout the description and claims, it is to be understood that this includes any of the purified compounds falling within this group as well as any of the comparatively impure mixtures such as the commercial grades mentioned above.
As set forth in the said application mentioned above, the phosphatide compound is added to the motor oil in a critical proportion range of about 0.01-2.0%. It is found that these percentages are critical in securing the desired improvement with respect to inhibiting bearing corrosion and lacquer formation and without affecting other desirable properties of the oil, while proportions above this range produce undue sludging. In the case of motor oils adapted for automotive use, a range of 0.01 to 0.25% appears most satisfactory, with about 0.1% preferred. Somewhat higher percentages may be employed in Diesel lubricating oil or airplane oil where it is desired to improve materially the ring sticking properties of the oil in addition to obtaining the benefits of inhibiting bearing corrosion and lacquer formation. A very satisfactory method for adding the phosphatide compound to the mineral lubricating oil is to first form a concentrate, such as a solution of the lecithin or other phosphatide compound in a S. A. E. 30 oil or other lubricating 011 within the motor oil viscosity range, and then add the concentrate to the mineral lubricating oil in an amount suflicient to give the desired percenta'g of phosphatide compound therein.
As set forth in said mentioned application, the phosphatide additive is particularly efl'ective in connection with highly solvent refined lubricat- 'varnish or lacquer formation. This lacquer generally appears as a yellowish or reddish brown film which deposits upon the metal surfaces, piston rings and cylinder walls during operation of the engine over extended periods of time. In the newest engines having extremely small clearances and high compression, this problem is so severe as to frequently result in seizure of the pistons when the motor is stopped and allowed to cool.
Further, the modern development of the highly refined motor oils together with the modern development of the new type bearings including the connecting rod and main bearings, of internal combustion engines, which has involved a departure from the old Babbitt bearings and has given rise to new alloy bearings of the type of cadmium-silver, has also presented the industry with the problem of bearing corrosion. This latter problem has been recognized for the last several years, and various materials have been heretofore suggested as additives for lubricating oil to inhibit such bearing corrosion. However, the materials heretofore suggested and used for this purpose, such as triphenyl phosphite, are ineffective in overcoming the more recent problem of lacquer formation. The phosphatide compound is unique in combining in one substance the properties of inhibiting or minimizing this objectionable lacquer formation and of also inhibiting bearing corrosion, reducing cylinder and piston wear, reducing oil ring and compression groove deposits and improving ring sticking of the motor oil to which the compound is added in the small proportion range specified above.
While the phosphatide additive is highly effective for the purposes stated, it is found that this addition seriously increases the emulsion difliculties of the oil when that oil comes in contact with water or salt water, as determined by the Navy emulsion test which is the United States Government Test No. 320.12 as found on page 76 et seq. of appendix 6-, Lubricants and Liquid Fuels, issued by the Navy Department August 1, 1928. with specifications set forth on page 7 of Naval Engineering Bulletin 31, Lubricating Oil, published by the U. S. Government Printing Office in 1937.
We have discovered that this difliculty can be effectively overcome by incorporating along with the phosphatide asmall amount of an emulsion preventing agent capable of improving the emulsion test of the oil in the presence of the phosphatide. We have further discovered that an oil soluble material which hydrolyzes in the presence of water to give an alkaline reaction is a very suitable agent for this purpose. For example, soaps of the alkali or alkaline earth metals, such as the stearates, palmitates, oleates, naphthenates, etc. of sodium, potassium, ammonium, lithium, calcium, etc., which can be dissolved in oil in small proportions, are effective for this purpose. The quaternary organic ammonium soaps ofthe general formula in which R, R, R", R' represent the same or different alkyl, aralkyl or aryl groups or combinations thereof, and in which x is a fatty acid or naphthenic acid radical, are also highly effective for this purpose. Moreover, compounds formed by substituting one or more of the hydrogens of the alkyl, aralkyl or aryl groups of such quaternary organic ammonium soaps with halogen, oxygen or sulfur, are also included. As an example of this type of compound, there may be mentioned tetrone B naphthenate, which is a quaternary ammonium soap and is believed to be trimethyl phenyl ammonium naphthenate (CaHs) (CHa)aN-naphthenate. We have found that agents of this type are effective in a small proportion range of about 0.02-0.9% by weight, higher percentages being employed in conjunction with the higher percentages of phosphatide additive. In the case of an automotive lubricant containing from about 0.01 to 0.25% of a phosphatide, the emulsion preventing agent is preferably used in the range of 0.02-0.5%. By way of example, a very satisfactory motor oil for automotive purposes is obtained by adding about 0.1% of a phosphatide, and about 0.10.2% of an emulsion preventing agent of the character of sodium naphthenate or tetrone B naphthenate.
We are aware that it has been heretofore suggested to add lecithin together with about 5% or less of a soap, such as sodium naphthenate, to
a light lubricating oil having a Saybolt viscosity of less than seconds at 100 F. to produce a textile fiber spraying oil (see U. S. Patent No. 2,002,885). The lecithin was employed here to improve the wetting or filming of the oil for the textile fibres and the soap was employed to assist in washing off the 011 after the fibres had been processed. The present invention is distinguished in the addition of lecithin to a different type of lubricating oil (a motor oil adapted for lubricating the bearings and cylinders of an internal combustion engine) which is of a different viscosity range as falling within the motor oil viscosity range and having a Saybolt viscosity in excess of 100 at 100 F. and generally in excess of 150 at 100 F. By a motor oil viscosity range, it is understood that this embraces the motor oils falling within the S. A. E. 10 to 60 grades as well as certain heavier motor oils adapted for special use in heavy duty truck or bus engines, at higher atmospheric temperatures and having a viscosity range varying from about 90 seconds at F. up to about seconds at 210 F. Saybolt Universal, as shown on page 444 of the 1936 edition of the S. A. E. Handbook. The present invention is further distinguished in that the lecithin is employed for an entirely different purpose of inhibiting lacquer formation and bearing corrosion, which are entirely new and unexpected properties unrelated to the fibre wetting or filming action of the prior art. The present invention is further distinguished in the use of a different and critical proportion range of "sodium naphthenate or other emulsion preventing agent for the different purpose of improving the emulsion test of the motor oil, which is remote from the detergent action of the soap of the prior art.
-in improving the Navy Emulsion Test oi lubribearing corrosion, as illustrated in the table set forth below:
eatin oi s tainin a sma l propo tion 01' a Concentration OloidolBT 1a.- 0.0 0.0 0.1 phosphatide, the following data is given: cimenmmn 0 percent" 0.0 0.1 0.1
Materials added :0 0i! 00101601 H0111 m K U MaterialA g Milli- Mllltmm- Cone. oimaterialA n g percent" 0.1 0.1 0.1 0.1 0.1 0.1 m 12 14 3 as 100 14 3 MaterialB 0 Sodium nephthenate 51 3 i5 3 2g 11:; 24 9 Cone. of material B 40 1g percent 0.0 0.1 0.07 0.02 0.1 0.1
sees sees sees sees were seas sees mass Reference oil was iuriural refined dewaxed Mid-Continent distillate S.A.E. grade.
i'Reierence oil was furiural refined dewaxed Mid-Continent distiliajtgflSAE. 20 grade.
The following table illustrates the effectiveness of quaternary organic ammonium soaps, such as tetrone B naphthenate in improving the Navy Emulsion Test of lubricating 011 containing a small proportion of a'phosphatide:
on S.A. E. S.A.E. $.A. E. B.A.E.
I Material A added Coloidol BT Material A percent-- 0.1 0. 1 0.1 0.1
Material B added Tetrone-B naphthenate Material B -.percent-. 0. 2 0. 15 0. 1 0. 05
Cc. oil separated:
15 min 40 3 1 30 min 40 4 1 m 40 4 1 00 min I 40 4 1 Ce. water separated:
rnln. 40 19 37 32 30 min 23 38 34 45 m 28 38 35 min 28 38 35 Cc. actual emulsion:
15 min 0 '21 40 47 30 min '17 38 45 45 min '12 38 44 00 min I '12 as 44 'Cufl.
The bearing corrosion test by which these data were obtained was carried out as follows:
A bushing lined with the same cadmium-silver or other alloy as employed in connecting rod bearings in some automotive engines, was immersed in a pot of oil to be tested, the oil being heated to a temperature of the order of 325-350 F. The oil was circulated between the bushing and its journal by a suitable propeller or "whirligig" for a period of five hours. The bushing was removed from the pot at intervals of five hours, weighed and returned. The loss in weight is expressed in milligrams and is considered the corrosion loss. The reference oil employedwas furfural refined dewaxed Mid-Continent lubricating oil of S. A. E. 30 grade.
In addition to the advantages enumerated above, it is found that these phosphatide compounds and particularly the purified compounds or the bleached soybean lecithin, and the emulsion preventing agents, such as the naphthenates prepared from purified naphthenic acids, can be added to high grade typical motor oils without objectionably aifecting desirable properties or tests of these oils as illustrated in the followin table:
Reference Reference oil plus oil additives Material A, added Coloidol BT. Material A- ercent Material B, added sodutgn naphthena Material B .-peroent 0.1 Gravity A P I 28. 2 Flash. 0 475 Fire, 0. 0 540 Viscosity, 1 526-528 Viscosity, 63-63 Color Lovlbond 6"- 300 Pour F -5 0 Carbon residue percent 0. 09-0. 10 0. 13-0. 11 Neut. N um r 0. 01 m. Number 0. 7-0. 6 mrmnt ,0]
Obviously many modifications and variations of the invention herein set forth may be made without departing from the spirit and scope thereof, and therefore only such limitations should be imposed-as are indicated in the appended claims.
We claim:
1. A motor oil for lubricating the bearings and cylinders of an internal combustion engine comprising a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about at F. to about at 210 F., containing about 0.01-2.0% of a phosphatide to inhibit bearing corrosion and lacquer formation and less than 1% of an emulsion preventing agent capable of improving the emulsion test of the oil in the presence of the phosphatide.
2. A motor oil according to claim 1 in which the emulsion preventing agent is an oi soluble material that hydrolyzes in the presence of water to give an alkaline reaction.
3. A motor oil according to claim 1 in which the emulsion preventing agent is an oil soluble soap of an alkali or alkaline earth metal.
4. A motor oil according to claim 1 in which the emulsion'preventing agent is a quaternary organic ammonium soap.
5. A motor oil according to claim 1 in which the emulsion preventing agent is a compound having the formula in which R, R, R", R' represent the same or different alkyl, aralkyl or aryl groups or combinations thereof, or halogen, oxygen and sulfur substituted derivatives thereof, and in which X represents a fatty acid or naphthenic acid' radical,
6. A motor oil according to claim 1 in which the emulsion preventing agent is an alkali metal naphthenate.
7. A motor oil according to claim 1 in which the emulsion preventing agent is sodium naphthenate.
8. A motor oil according to claim 1 in which the emulsion preventing agent is potassium naphthenate.
9. A motor oil according to claim 1 in which the emulsion preventing agent is trimethyl phenyl ammonium naphthenate.
10. A motor oil for lubricating the bearings and cylinders of an internal combustion engine, comprising a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about at F, to about at 210 F., containing about 0.012.0% of a lecithin, and about 0.02-0.9% of an emulsion preventing agent capable of improving the emulsion test of the oil in the presence of the lecithin.
11. A motor oil for lubricating the bearings and cylinders of an internal combustion engines, comprising a highly solvent refined mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 containing about 0.01-0.257. of a phosphatide and about 0.02-0.5% of an emulsion preventing agent which is oil soluble and which hydrolyzes in the presence of water to give an alkaline reaction.
12. A motor oil for lubricating bearings and cylinders of an internal combustion engine, comprising a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing about 0.1% of a phosphatide and about 0.l-0.2% of an oil soluble soap of an alkali or alkaline earth metal which acts as an agent capable of improving the emulsion test of the oil in the presence of the phosphatide.
13. A motor oil for lubricating bearings and cylinders of an internal combustion engine, comprising a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing about 0.1% of a bleached commercial soybean lecithin and about 0.1% of sodium naphthenate'.
14. The method of lubricating bearings and cylinders of an internal combustion engine, which comprises supplying to the bearings and cylinders of said engine a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing a small proportion of a phosphatide of the order of about 0.01-2.0% suillcient to inhibit bearing corrosion and lacquer formation, and containing less than about 1% of an agent capable of improving the emulsion test of the oil in the presence of the phosphatide.
15. The method of lubricating bearings and cylinders of an internal combustion engine, which comprises supplying to the bearings and cylinders of said engine a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing less than about 1% of a phosphatide and containing less than about 1% of an oil soluble soap of an alkali or alkaline earth metal capable of improving the emulsion test of the oil in the presence of the phosphatide.
16. The method of lubricating the bearings and cylinders in an internal combustion engine, which comprises supplying to the bearings and cylinders of said engine a highly solvent refined mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing about 0.010.25% of a phosphatide to inhibit bearing corrosion and lacquer formation, and about 0.02-0.5% of an agent capable of improving the emulsion test of the oil in the presence of the phosphatide.
17. The method of lubricating the bearings and cylinders in an internal combustion engine, which comprises supplying to the bearings and cylinders of said engine a highly solvent refined mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 F., containing about 0.1% of a phosphatide to inhibit bearing corrosion and lacquer formation and about 0.0l0.2% of an oil soluble soap of an alkali or alkaline earth metal capable of improving the emulsion test of the oil in the presence of the phosphatide.
18. The method of lubricating the bearings, cylinders and pistons of an internal combustion engine, which comprises supplying to the bearings, cylinders and pistons of said engine a mineral lubricating oil within the motor oil viscosity range having a Saybolt viscosity of from about 90 at 130 F. to about 150 at 210 R, which lubri eating oil of itself would normally cause corrosion of said bearings and lacquer formation on said pistons, incorporating in said mineral lubricating oil about 0.01-2.0% of a phosphatide to inhibit said bearing corrosion and lacquer formation but which is suflicient to increase the emulsion difliculties of the oil in the presence of watar as determined by the Navy emulsion test, and also incorporating in said oil about 0.02-0.9% of an alkali metal naphthenate to improve the said oil containing the phosphatide with respect to said emulsion test.
HARRY V. ASHBURN.
WILLIAM G. ALSOP.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US223527A US2221162A (en) | 1938-08-06 | 1938-08-06 | Lubricating oil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US223527A US2221162A (en) | 1938-08-06 | 1938-08-06 | Lubricating oil |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2221162A true US2221162A (en) | 1940-11-12 |
Family
ID=22836897
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US223527A Expired - Lifetime US2221162A (en) | 1938-08-06 | 1938-08-06 | Lubricating oil |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2221162A (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2415353A (en) * | 1944-03-15 | 1947-02-04 | Standard Oil Dev Co | Rust preventing turbine oil |
| US2430951A (en) * | 1943-11-27 | 1947-11-18 | Standard Oil Co | Corrosion inhibiting compositions |
| US2431652A (en) * | 1943-09-03 | 1947-11-25 | American Lecithin Co | Sulphur-containing phosphatide, lubricant, and method of making |
| US2458535A (en) * | 1943-12-29 | 1949-01-11 | Shappirio Sol | Modified hydrocarbon compositions and petroleum distillates |
| US3017283A (en) * | 1959-04-30 | 1962-01-16 | Reichard Coulston Inc | Corrosion inhibitive pigment |
| US3070500A (en) * | 1955-07-12 | 1962-12-25 | Buer Carl Heinz | Process for preparing stable alcoholic emulsion of grape sugar |
| US3255108A (en) * | 1961-08-30 | 1966-06-07 | Lubrizol Corp | Water-in-oil emulsions containing succinic esters |
| US4599185A (en) * | 1985-03-25 | 1986-07-08 | Borg-Warner Corporation | Refrigerant additive and method for reducing corrosion in refrigeration systems |
| US4600518A (en) * | 1985-07-15 | 1986-07-15 | Nalco Chemical Company | Choline for neutralizing naphthenic acid in fuel and lubricating oils |
| US5120357A (en) * | 1991-02-06 | 1992-06-09 | Amico, Inc. | Lecithin corrosion inhibitor |
| US5135669A (en) * | 1989-03-09 | 1992-08-04 | Exxon Chemical Patents Inc. | Hydrogenated lecithin for friction and flow properties |
| WO2014150099A1 (en) * | 2013-03-14 | 2014-09-25 | Buckman Laboratories International, Inc. | Modified lecithin corrosion inhibitor in fluid systems |
-
1938
- 1938-08-06 US US223527A patent/US2221162A/en not_active Expired - Lifetime
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2431652A (en) * | 1943-09-03 | 1947-11-25 | American Lecithin Co | Sulphur-containing phosphatide, lubricant, and method of making |
| US2430951A (en) * | 1943-11-27 | 1947-11-18 | Standard Oil Co | Corrosion inhibiting compositions |
| US2458535A (en) * | 1943-12-29 | 1949-01-11 | Shappirio Sol | Modified hydrocarbon compositions and petroleum distillates |
| US2415353A (en) * | 1944-03-15 | 1947-02-04 | Standard Oil Dev Co | Rust preventing turbine oil |
| US3070500A (en) * | 1955-07-12 | 1962-12-25 | Buer Carl Heinz | Process for preparing stable alcoholic emulsion of grape sugar |
| US3017283A (en) * | 1959-04-30 | 1962-01-16 | Reichard Coulston Inc | Corrosion inhibitive pigment |
| US3255108A (en) * | 1961-08-30 | 1966-06-07 | Lubrizol Corp | Water-in-oil emulsions containing succinic esters |
| US4599185A (en) * | 1985-03-25 | 1986-07-08 | Borg-Warner Corporation | Refrigerant additive and method for reducing corrosion in refrigeration systems |
| US4600518A (en) * | 1985-07-15 | 1986-07-15 | Nalco Chemical Company | Choline for neutralizing naphthenic acid in fuel and lubricating oils |
| US5135669A (en) * | 1989-03-09 | 1992-08-04 | Exxon Chemical Patents Inc. | Hydrogenated lecithin for friction and flow properties |
| US5120357A (en) * | 1991-02-06 | 1992-06-09 | Amico, Inc. | Lecithin corrosion inhibitor |
| WO2014150099A1 (en) * | 2013-03-14 | 2014-09-25 | Buckman Laboratories International, Inc. | Modified lecithin corrosion inhibitor in fluid systems |
| US10060038B2 (en) | 2013-03-14 | 2018-08-28 | Buckman Laboratories International, Inc. | Modified lecithin corrosion inhibitor in fluid systems |
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