US2168674A - Lubricant - Google Patents
Lubricant Download PDFInfo
- Publication number
- US2168674A US2168674A US114435A US11443536A US2168674A US 2168674 A US2168674 A US 2168674A US 114435 A US114435 A US 114435A US 11443536 A US11443536 A US 11443536A US 2168674 A US2168674 A US 2168674A
- Authority
- US
- United States
- Prior art keywords
- bearings
- alkyl
- oils
- cadmium
- corrosive
- 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 9
- -1 octyl isocyanate phenyl isocyanate isobutyl isocyanate propyl isocyanate Chemical compound 0.000 description 22
- 239000010687 lubricating oil Substances 0.000 description 13
- 238000005260 corrosion Methods 0.000 description 10
- 230000007797 corrosion Effects 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 9
- NSAODVHAXBZWGW-UHFFFAOYSA-N cadmium silver Chemical compound [Ag].[Cd] NSAODVHAXBZWGW-UHFFFAOYSA-N 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 229910045601 alloy Inorganic materials 0.000 description 7
- 239000000956 alloy Substances 0.000 description 7
- 238000002485 combustion reaction Methods 0.000 description 7
- WIKSRXFQIZQFEH-UHFFFAOYSA-N [Cu].[Pb] Chemical group [Cu].[Pb] WIKSRXFQIZQFEH-UHFFFAOYSA-N 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- OJIJEKBXJYRIBZ-UHFFFAOYSA-N cadmium nickel Chemical compound [Ni].[Cd] OJIJEKBXJYRIBZ-UHFFFAOYSA-N 0.000 description 6
- XLJMAIOERFSOGZ-UHFFFAOYSA-N cyanic acid Chemical compound OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 description 6
- 229910001092 metal group alloy Inorganic materials 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- 229910000978 Pb alloy Inorganic materials 0.000 description 5
- 150000005840 aryl radicals Chemical class 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 4
- 230000001050 lubricating effect Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- OWIKHYCFFJSOEH-UHFFFAOYSA-N Isocyanic acid Chemical compound N=C=O OWIKHYCFFJSOEH-UHFFFAOYSA-N 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000010705 motor oil Substances 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- 150000003254 radicals Chemical group 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 229910000897 Babbitt (metal) Inorganic materials 0.000 description 1
- 229910000713 I alloy Inorganic materials 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000001412 amines Chemical group 0.000 description 1
- METKIMKYRPQLGS-UHFFFAOYSA-N atenolol Chemical compound CC(C)NCC(O)COC1=CC=C(CC(N)=O)C=C1 METKIMKYRPQLGS-UHFFFAOYSA-N 0.000 description 1
- 239000001996 bearing alloy Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- DMCJFWXGXUEHFD-UHFFFAOYSA-N diheptadecyl ketone Natural products CCCCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCCCCCC DMCJFWXGXUEHFD-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- YJMNOKOLADGBKA-UHFFFAOYSA-N naphthalene-1-carbonitrile Chemical compound C1=CC=C2C(C#N)=CC=CC2=C1 YJMNOKOLADGBKA-UHFFFAOYSA-N 0.000 description 1
- PLZZPPHAMDJOSR-UHFFFAOYSA-N nonanenitrile Chemical compound CCCCCCCCC#N PLZZPPHAMDJOSR-UHFFFAOYSA-N 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- XAHRZZCLDVBCBJ-UHFFFAOYSA-N s-cyano octadecanethioate Chemical group CCCCCCCCCCCCCCCCCC(=O)SC#N XAHRZZCLDVBCBJ-UHFFFAOYSA-N 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- RHSBIGNQEIPSCT-UHFFFAOYSA-N stearonitrile Chemical compound CCCCCCCCCCCCCCCCCC#N RHSBIGNQEIPSCT-UHFFFAOYSA-N 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical group [SH] PXQLVRUNWNTZOS-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
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- 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
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty 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
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C10M2215/082—Amides [having hydrocarbon substituents containing less than thirty carbon atoms] containing hydroxyl groups; Alkoxylated 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/16—Nitriles
-
- 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
- C10M2215/28—Amides; Imides
-
- 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
- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
-
- 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
Definitions
- This invention relates to lubricants and, in particular, to addition agents imparting to lubricants improved properties.
- Our invention has particular utility in preventing and/or inhibiting the corrosion of hard metal alloy bearings such as copper-lead, cadmiumnickel, and cadmium-silver bearings which, to a large extent, have replaced soft metal bearings such as Babbitt metal in the trend toward internal combustion engines having high compression ratios and increased acceleration and increased speed characteristics.
- hard metal alloy bearings such as copper-lead, cadmiumnickel, and cadmium-silver bearings
- soft metal bearings such as Babbitt metal in the trend toward internal combustion engines having high compression ratios and increased acceleration and increased speed characteristics.
- the use of the hard metal bearings has created lubricatingand corrosion problems, particularly in connection with highly refined oils, some of which may be very corrosive to the hard metal bearings.
- highly refined lubricating oils we mean viscous oils which have a minimum viscosity in the range of S. A. E. 10 oils, and which'have been subjected to such refining processes such as, for example, solvent extraction, that the parafiinicity of the oil is markedly increased. It has been found that highly refined lubricating oils cause corrosion to alloy bearings of the cadmium-silver type to the extent of 5 mg/cm. and even greater when such bearings are submerged for hours or less in an air agitated oil which has been preoxidized at about 340 F. for 25 to 50 hours.
- the motor oils may be highly refined lubricating oils as such or mixtures of highly refined lubricating oils with less highly refined lubricating oils, or stated in another way, mixtures of corrosive oils and non-corrosive oils, examples of the latter being lubricating oil fractions from Winkler crude or crudes of the Winkler type.
- alkyl or aryl derivatives as used herein include the alkyl and aryl radicals and said radicals substituted with alkoxy, amines, mercapto, halogen or other substituent group or groups and/ or mixtures thereof.
- alkyl or aryl derivatives of cyanic acid and isocyanic acid which have the general formula ROCN or RNCO in which R is an alkyl or aryl radical:
- octyl isocyanate phenyl isocyanate isobutyl isocyanate propyl isocyanate examples of the alkyl. or aryl derivatives of hydrocyanic acid and isohydrocyanic acid having the general formula RCN or RNC in which R is an alkyl or aryl radical are listed below:
- octyl cyanide cetyl nitrile trimethyl acetonitrile phenyl acetonitrile lauryl nitrile alpha naphthyl nitrile stearonitrile benzonitrile octyl isocyanide
- R is an alkyl radical, such as .lauroyl thiocyanate, stearoyl thiocyanate, etc.
- thiocyan ketones having the general formula in which R and R are alkyl radicals such as alpha thiocyanoamyl-butyl ketone, alpha thiocyano stearone, etc.
- These compounds may also be used to impart other desirable properties to lubricating oils such as non-stickingring properties and the like.
- cadmium-nickel and copper-lead alloys which comprises-applying to said bearings a lubricant comprising a highly refined lubricating oil normally corrosive to said bearings and ahydrocarbon isocyanate having the general formula RNCO in which R.” is a hydrocarbon group, said hydrocarbon isocyanate being used in a small but suflicient proportion to substantially inhibit the corrosion of said bearings.
- cadmium-nickel and copper-lead alloys which comprises applying to said bearings a lubricant comprising .a highly refined lubricating oil normally corrosive to said bearings and an alkyl cyanide having the general formula RUN in which R is an alkyl radical, said alkyl cyanide being used in a small but suflicient proportion to substantially inhibit the corrosion of said bearings.
- the method of lubricating internal combustion engines provided with hard metal alloy bearings having the corrosive susceptibility of alloys of the class consisting of cadmium-silver, cadmium-nickel and copper-lead alloys, which comprises applying to'said bearings a lubricant comprising a highly refined lubricating oil normally corrosive to said bearings and an aryl cyanide having the general formula RCN in which R" is an aryl radical, said aryl cyanide being used in a small butsuflicient proportion to substantially inhibit the corrosion of said bearings.
- the methodof lubricating internal com-' bustionengines provided with hard metal alloy bearings having the corrosive susceptibility of alloys of the class consisting of, cadmiumsilver, cadmium-nickel and copper-lead alloys which comprises applying to said bearings a lubricant comprising a highly refined lubricating oil nor- -mally corrosive to said bearings and, an organic compound selected from the group consisting of hydrocarbon cyanates having the general formula RDCN, hydrocarbon isocyanates having the general formula RNCO', hydrocarbon cyanides having the general formula RCN, and hydrocarbon isocyanides having the general formula RNC,vin which 'R in each instance is a radical selected from the group consisting of. alkyl radicals and aryl radicals; said organic compound being used in a, small but sufilcient proportion to substantially inhibit the corrosion or said bearings.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
?ateni:eri Aug. 8, 1939 taunt i i E e i e LUBRICANT diana No Drawing. Application December 5, 1936, Serial No. 1l4,435
4 Claims.
This invention relates to lubricants and, in particular, to addition agents imparting to lubricants improved properties.
Our invention has particular utility in preventing and/or inhibiting the corrosion of hard metal alloy bearings such as copper-lead, cadmiumnickel, and cadmium-silver bearings which, to a large extent, have replaced soft metal bearings such as Babbitt metal in the trend toward internal combustion engines having high compression ratios and increased acceleration and increased speed characteristics. The use of the hard metal bearings has created lubricatingand corrosion problems, particularly in connection with highly refined oils, some of which may be very corrosive to the hard metal bearings.
By highly refined lubricating oils we mean viscous oils which have a minimum viscosity in the range of S. A. E. 10 oils, and which'have been subjected to such refining processes such as, for example, solvent extraction, that the parafiinicity of the oil is markedly increased. It has been found that highly refined lubricating oils cause corrosion to alloy bearings of the cadmium-silver type to the extent of 5 mg/cm. and even greater when such bearings are submerged for hours or less in an air agitated oil which has been preoxidized at about 340 F. for 25 to 50 hours. The motor oils may be highly refined lubricating oils as such or mixtures of highly refined lubricating oils with less highly refined lubricating oils, or stated in another way, mixtures of corrosive oils and non-corrosive oils, examples of the latter being lubricating oil fractions from Winkler crude or crudes of the Winkler type.
We have found that corrosion of hard metal bearing alloys of the cadmium-silver type due to corrosive highly refined lubricating oil can be inhibiting and other desirable properties can be imparted to lubricating oils by adding to said oils certain organic compounds, particularly the alkyl or aryl derivatives of an acid selected from the group consisting of cyanic acid, isocyanic acid, hydrocyanic acid and isohydrocyanic acid. The
' terms alkyl or aryl derivatives as used herein include the alkyl and aryl radicals and said radicals substituted with alkoxy, amines, mercapto, halogen or other substituent group or groups and/ or mixtures thereof.
Below are examples of alkyl or aryl derivatives of cyanic acid and isocyanic acid which have the general formula ROCN or RNCO in which R is an alkyl or aryl radical:
octyl isocyanate phenyl isocyanate isobutyl isocyanate propyl isocyanate Examples of the alkyl. or aryl derivatives of hydrocyanic acid and isohydrocyanic acid having the general formula RCN or RNC in which R is an alkyl or aryl radical are listed below:
octyl cyanide cetyl nitrile trimethyl acetonitrile phenyl acetonitrile lauryl nitrile alpha naphthyl nitrile stearonitrile benzonitrile octyl isocyanide In addition'to the alkyl or aryl derivatives of the cyanic acids and the hydrocyanic acids we may use the fatty acid thiocyanates having the general formula in which R is an alkyl radical, such as .lauroyl thiocyanate, stearoyl thiocyanate, etc. We may also use the thiocyan ketones having the general formula in which R and R are alkyl radicals such as alpha thiocyanoamyl-butyl ketone, alpha thiocyano stearone, etc.
While we may use any alkyl or aryl derivative of the hereinbefore disclosed acids we prefer to use those derivatives having a boiling point of about 400 F. or higher in order to avoid volatization of the addition agent at the temperature attained in internal combustion engines during operation.
As has been heretofore mentioned many of the recent models of automobiles now in use are equipped with bearings of the hard metal alloy type such as cadmium-silver alloy, cadmiumnickel alloy, copper-lead alloy, etc. for the purpose of permitting increased speed characteristics and increased acceleration. Also in recent years mineral lubricating oils adapted for use in internal combustion engines have been more drastically refined by acid treatment and/or solventextraction for the purpose of improving certain properties thereof suchas the viscosity index, sludge stability and the like. While oils so refined give satisfactory performance in many respects they have been found to cause more or less trouble in internal combustion engines equipped with bearings of the cadmium-silver type due to the corrosion of such alloys. We have found that the addition of very small amounts, such as 0.01% to 0.75% of the compounds hereinbefore disclosed, to corrosive highly refined motor oils will inhibit the corrosion of such alloys.
These compounds may also be used to impart other desirable properties to lubricating oils such as non-stickingring properties and the like.
Under certain conditions some of the compounds falling within the class herein disclosed may not be completely soluble in the lubricant,
as defined by the appended claims.
We claim: f
1. The method of lubricating internal combustion engines provided with hard metal alloy bearings having the corrosive susceptibility of alloys of the class consisting of cadmium-silver,
cadmium-nickel and copper-lead alloys, which comprises-applying to said bearings a lubricant comprising a highly refined lubricating oil normally corrosive to said bearings and ahydrocarbon isocyanate having the general formula RNCO in which R." is a hydrocarbon group, said hydrocarbon isocyanate being used in a small but suflicient proportion to substantially inhibit the corrosion of said bearings. -v
2. The method of lubricating internal combus tion engines provided with hard metal alloy bearings having thecorrosive susceptibility of I alloys of the class consisting of cadmium-silver,
cadmium-nickel and copper-lead alloys,- which comprises applying to said bearings a lubricant comprising .a highly refined lubricating oil normally corrosive to said bearings and an alkyl cyanide having the general formula RUN in which R is an alkyl radical, said alkyl cyanide being used in a small but suflicient proportion to substantially inhibit the corrosion of said bearings.
3. The method of lubricating internal combustion engines provided with hard metal alloy bearings having the corrosive susceptibility of alloys of the class consisting of cadmium-silver, cadmium-nickel and copper-lead alloys, which comprises applying to'said bearings a lubricant comprising a highly refined lubricating oil normally corrosive to said bearings and an aryl cyanide having the general formula RCN in which R" is an aryl radical, said aryl cyanide being used in a small butsuflicient proportion to substantially inhibit the corrosion of said bearings.
4; The methodof lubricating internal com-' bustionengines provided with hard metal alloy bearings having the corrosive susceptibility of alloys of the class consisting of, cadmiumsilver, cadmium-nickel and copper-lead alloys which comprises applying to said bearings a lubricant comprising a highly refined lubricating oil nor- -mally corrosive to said bearings and, an organic compound selected from the group consisting of hydrocarbon cyanates having the general formula RDCN, hydrocarbon isocyanates having the general formula RNCO', hydrocarbon cyanides having the general formula RCN, and hydrocarbon isocyanides having the general formula RNC,vin which 'R in each instance is a radical selected from the group consisting of. alkyl radicals and aryl radicals; said organic compound being used in a, small but sufilcient proportion to substantially inhibit the corrosion or said bearings. l
' CLARENCE M. LOANE.
BERNARD H. SHOEMAKER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US114435A US2168674A (en) | 1936-12-05 | 1936-12-05 | Lubricant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US114435A US2168674A (en) | 1936-12-05 | 1936-12-05 | Lubricant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2168674A true US2168674A (en) | 1939-08-08 |
Family
ID=22355187
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US114435A Expired - Lifetime US2168674A (en) | 1936-12-05 | 1936-12-05 | Lubricant |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2168674A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2682336A (en) * | 1950-01-04 | 1954-06-29 | Phillips Petroleum Co | Rubber swelling additives for fuels |
| US2723944A (en) * | 1954-02-03 | 1955-11-15 | Universal Oil Prod Co | Treatment of hydrocarbon distillates with isocyanates |
| US3376220A (en) * | 1966-03-25 | 1968-04-02 | Chevron Res | Polycyano lubricating oil detergents |
| US4717754A (en) * | 1979-09-12 | 1988-01-05 | Exxon Research & Engineering Co. | Oil additives containing a thiocarbamyl moiety |
| US4794146A (en) * | 1980-01-07 | 1988-12-27 | Exxon Research & Engineering Co. | Oil additives containing a thiocarbamyl moiety |
| US4910263A (en) * | 1980-01-07 | 1990-03-20 | Exxon Research & Engineering Company | Oil additives containing a thiocarbamyl moiety |
-
1936
- 1936-12-05 US US114435A patent/US2168674A/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2682336A (en) * | 1950-01-04 | 1954-06-29 | Phillips Petroleum Co | Rubber swelling additives for fuels |
| US2723944A (en) * | 1954-02-03 | 1955-11-15 | Universal Oil Prod Co | Treatment of hydrocarbon distillates with isocyanates |
| US3376220A (en) * | 1966-03-25 | 1968-04-02 | Chevron Res | Polycyano lubricating oil detergents |
| US4717754A (en) * | 1979-09-12 | 1988-01-05 | Exxon Research & Engineering Co. | Oil additives containing a thiocarbamyl moiety |
| US4794146A (en) * | 1980-01-07 | 1988-12-27 | Exxon Research & Engineering Co. | Oil additives containing a thiocarbamyl moiety |
| US4910263A (en) * | 1980-01-07 | 1990-03-20 | Exxon Research & Engineering Company | Oil additives containing a thiocarbamyl moiety |
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