US2385964A - Lubricant - Google Patents
Lubricant Download PDFInfo
- Publication number
- US2385964A US2385964A US510037A US51003743A US2385964A US 2385964 A US2385964 A US 2385964A US 510037 A US510037 A US 510037A US 51003743 A US51003743 A US 51003743A US 2385964 A US2385964 A US 2385964A
- Authority
- US
- United States
- Prior art keywords
- thiol
- oil
- carbamate
- addition
- dithiocarbamate
- 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
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
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/12—Thio-acids; Thiocyanates; Derivatives thereof
- C10M135/14—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond
- C10M135/18—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond thiocarbamic type, e.g. containing the groups
-
- 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
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
- C10M2219/066—Thiocarbamic type compounds
-
- 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
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
- C10M2219/066—Thiocarbamic type compounds
- C10M2219/068—Thiocarbamate metal salts
-
- 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
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/102—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon only in the 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
-
- 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
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/106—Thiadiazoles
Definitions
- This invention relates to lubricants and in particular, it relates to addition agents imparting to lubricants increased stability towards oxidation and sludge formation.
- My invention is particularly useful in retarding the formation of insoluble material usually called sludge, in lubricants.
- This solid and sludgy matter results from the action of atmospheric oxygen upon certain constituents of lubricants in the presence or in the absence of metals such as, for example, alloy bearings of the copperlead, cadmium-nickel, or cadmium-silver types. Elevated temperatures such as those encountered in automotive crank ca'ses accelerate this sludge formation.
- Many chemical compounds and materials have been proposed as addition agents which when added to lubricants may improved one or more of the properties thereof, for example, increase viscosity index of the oil, increase the oiliness or film strength, or decrease the corrosiveness thereof. some of these addition agents while, for example, improving the oiliness or film strength of the oil, may have no effect on these other properties, or may even be deleterious as regards other characteristics.
- An object of my invention is to provide a lubricant having reduced oxidation and sludge formation tendencies.
- Another object of my invention is to provide a lubricant having generally improved qualities as well as reduced oxidation and sludge formation tendencies obtained by the addition of one or more agents or materials.
- R and B. may be alike or diflerent. Any of these groups may contain substituted nitro, halogen, amino and/or hydroxy groups.
- Primary aromatic amines, such as aniline, are an exception in that they continue-the reaction to form substituted thioureas in place of the carbamates.
- dithiocarbamates to lubricating oils in concentrations from less than 0.005% to approximately 1% by weight, efiects a marked increase in the stability of the oils toward oxidation and sludge formation.
- the viscosity index of the dithiocarbamate treated oils is somewhat increased, as well as the pour point being lowered.
- Other properties of the oils, such as lubricity, oiliness, and film strength may also be improved.
- Table I indicates the results of Indiana oxidation tests of an unstable oil containing 0.005 to Piperidine dithiocerbamate Pipecoline dithiocarbamate. Piperazine ditniocarbamate Di-n-butyl thiol thiono carbamate. Bi-di-iso amyl thiol thiono carbamate Tetra hydro quinoline dithio carbamate Exmrra II The addition of 0.005% by weight of pipecoline methyl hexamethylene dithiocarbamate to a lubricating oil forming 10 milligrams of sludge per 10 grams of oil in 22 hours by Indiana oxidation extended the 10 milligram period to 28 hours.
- the viscosity index or the oil cited in Example II was increased from 94 to 97 by that additive.
- the groups RR may be a cycle t ns
- V. I. of this same oil was increased from 94 to 98.5 by the addition oi 0.005% dipiperazyl thiol thiono carbamate.
- dithiocarbamate is synonymous with the grouping thiol thiono carbamate.
- thiocarbamic acid namely, HsN-CS-OH
- HsN-CS-SH a dithiocarbamic acid
- the -SH group is called the thiol group.
- thiol thiono carbamates or dithiocarbamates a molecule containing both groups, as in the compounds disclosed, may be termed thiol thiono carbamates or dithiocarbamates and refer to the same molecule.
- di-nbutyl thiol thiono carbamate is the same molecule as di-n-butyl dithiocarbamate; similarly bi-diisoamyi thiol thlono carbamate is synonymous within the scope of my invention.
- An improved lubricating oil composition comprising a mineral lubricating oil having incorporated therein a small quantity of bi-di-isoamyi thiol thlono carbamate sufficient to increase the stability of the so treated lubricating 011 against oxidation and sludge formation at crank case temperatures.
- An improved lubricating oil composition comprising a mineral lubricating oil havin incorporated therein from 0.005% to,0.05% by weight 01' bi-di-isoamyl thiol thiono carbamate to increase the stability 01. the so treated lubrieating oil against oxidation and sludge formation at crank case temperatures.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Oct. 2, 1945 LUBRICANT Daniel E. Bergen, Phillips, Tex asslgnor to Phillips Petroleum Company, a corporation oi Delaware No Drawing. Original application December 19,
1940, Serial No.
370,903, now Patent No.
2,343,393, dated March 7, 1944. Divided and this application November 12, 1943, Serial No.
This invention relates to lubricants and in particular, it relates to addition agents imparting to lubricants increased stability towards oxidation and sludge formation.
This application is a division of my copending application, Serial Number 370,903, filed December 19, 1940, and which has been issued as Patent No. 2,343,393 on March '7, 1944.
My invention is particularly useful in retarding the formation of insoluble material usually called sludge, in lubricants. This solid and sludgy matter results from the action of atmospheric oxygen upon certain constituents of lubricants in the presence or in the absence of metals such as, for example, alloy bearings of the copperlead, cadmium-nickel, or cadmium-silver types. Elevated temperatures such as those encountered in automotive crank ca'ses accelerate this sludge formation. Many chemical compounds and materials have been proposed as addition agents which when added to lubricants may improved one or more of the properties thereof, for example, increase viscosity index of the oil, increase the oiliness or film strength, or decrease the corrosiveness thereof. some of these addition agents while, for example, improving the oiliness or film strength of the oil, may have no effect on these other properties, or may even be deleterious as regards other characteristics.
An object of my invention is to provide a lubricant having reduced oxidation and sludge formation tendencies.
Another object of my invention is to provide a lubricant having generally improved qualities as well as reduced oxidation and sludge formation tendencies obtained by the addition of one or more agents or materials.
Still other objects and advantages will be apparent to those skilled in the art by a careful study of the following disclosure.
3: have found that the addition of dithiocarbamate to lubricating oils causes a marked increase in the stability of the oils toward oxidation and sludg formation.
Most primary and secondary organic amines react with carbon disulnde to form dithiocarbamates having the general formula,
R\ s R N-C:S;I\ a" 11 R in which R and B. may be hydrogen and/or normal or iso-alkyl; alicyclic; aryl; aryl-alkyl groups; or nitrogen, sulfur or oxygen heterocyclic 2 Claims. (01. 252-47) ing the amino nitrogen atom in the ring, such as in the secondary amines resulting from the partial or complete reduction of nitrogen heterocyclics. R and B. may be alike or diflerent. Any of these groups may contain substituted nitro, halogen, amino and/or hydroxy groups. Primary aromatic amines, such as aniline, are an exception in that they continue-the reaction to form substituted thioureas in place of the carbamates.
The use of the thioureas as additives to lubricating oils is known.
The addition of these dithiocarbamates to lubricating oils in concentrations from less than 0.005% to approximately 1% by weight, efiects a marked increase in the stability of the oils toward oxidation and sludge formation. In addition, the viscosity index of the dithiocarbamate treated oils is somewhat increased, as well as the pour point being lowered. Other properties of the oils, such as lubricity, oiliness, and film strength may also be improved.
The following examples will illustrate the improvement in these properties by the addition of the dithiocarbamates, but I do not wish to limit my invention by the specific examples.
EXAMPLE I Table I indicates the results of Indiana oxidation tests of an unstable oil containing 0.005 to Piperidine dithiocerbamate Pipecoline dithiocarbamate. Piperazine ditniocarbamate Di-n-butyl thiol thiono carbamate. Bi-di-iso amyl thiol thiono carbamate Tetra hydro quinoline dithio carbamate Exmrra II The addition of 0.005% by weight of pipecoline methyl hexamethylene dithiocarbamate to a lubricating oil forming 10 milligrams of sludge per 10 grams of oil in 22 hours by Indiana oxidation extended the 10 milligram period to 28 hours.
as m
The viscosity index or the oil cited in Example II was increased from 94 to 97 by that additive.
groups. The groups RR may be a cycle t ns Similarly, the V. I. of this same oil was increased from 94 to 98.5 by the addition oi 0.005% dipiperazyl thiol thiono carbamate.
EXAMPLE IV The pour point of a waxy oil was lowered from 40 to 25 F. by the addition of 0.005% of dipiperazyl thiol thiono carbamate.
In describing this aforementioned type 0! sulfur containing compounds, it might be mentioned that the term dithiocarbamate is synonymous with the grouping thiol thiono carbamate. The structural formula for carbamic acid,
is well known, and is a derivative similar in structure to the urea molecule, while thiocarbamic acid, namely, HsN-CS-OH, may be considered in a similar relation to thiourea. The second or remaining oxygen in this thiocarbamic acid molecule may be replaced by a sulfur atom yielding a dithiocarbamic acid, HsN-CS-SH. This ==C=S group is known as the thiono group, while the -SH group is called the thiol group. Hence, a molecule containing both groups, as in the compounds disclosed, may be termed thiol thiono carbamates or dithiocarbamates and refer to the same molecule. For example, di-nbutyl thiol thiono carbamate is the same molecule as di-n-butyl dithiocarbamate; similarly bi-diisoamyi thiol thlono carbamate is synonymous within the scope of my invention.
1. do not wish to limit my invention to the specific examples given since many dithiocarbamate molecules prepared from the amines and containing the radicals given above serve within degree toimprove the properties or characteristics oi mineral lubricating oils and yet remain within the scope of my invention.
I claim:
1. An improved lubricating oil composition comprising a mineral lubricating oil having incorporated therein a small quantity of bi-di-isoamyi thiol thlono carbamate sufficient to increase the stability of the so treated lubricating 011 against oxidation and sludge formation at crank case temperatures.
2. An improved lubricating oil composition comprising a mineral lubricating oil havin incorporated therein from 0.005% to,0.05% by weight 01' bi-di-isoamyl thiol thiono carbamate to increase the stability 01. the so treated lubrieating oil against oxidation and sludge formation at crank case temperatures.
DANIEL E. BERGEN.
CERTIFICATE OF CORRECTI 0N.
Patent No. 2,585,96L
- DANIEL E.
October 2, i9i 5.
BERGEN It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as follows: Page 2, second column, line 5, strike out the words "within the scope of my invention" and insert instead --with bi-di-isoamyl dithiocarbamate-; and that the said Letters Patent should be read with this correction therein that the same may conform to the record of the case in the Patent Office.
Signed. and sealed this 25th day of December, A. D. 1915.
(Seal) Leslie Frazer First Assistant Commissioner of Patents.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US508381A US2368106A (en) | 1940-12-19 | 1943-10-30 | Lubricant |
US510037A US2385964A (en) | 1940-12-19 | 1943-11-12 | Lubricant |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US370903A US2343393A (en) | 1940-12-19 | 1940-12-19 | Lubricant |
US508381A US2368106A (en) | 1940-12-19 | 1943-10-30 | Lubricant |
US510037A US2385964A (en) | 1940-12-19 | 1943-11-12 | Lubricant |
Publications (1)
Publication Number | Publication Date |
---|---|
US2385964A true US2385964A (en) | 1945-10-02 |
Family
ID=27408992
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US508381A Expired - Lifetime US2368106A (en) | 1940-12-19 | 1943-10-30 | Lubricant |
US510037A Expired - Lifetime US2385964A (en) | 1940-12-19 | 1943-11-12 | Lubricant |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US508381A Expired - Lifetime US2368106A (en) | 1940-12-19 | 1943-10-30 | Lubricant |
Country Status (1)
Country | Link |
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US (2) | US2368106A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2765277A (en) * | 1951-11-21 | 1956-10-02 | Exxon Research Engineering Co | Lubricating oil additives |
US2785129A (en) * | 1951-07-03 | 1957-03-12 | Texas Co | Lubricating compositions containing 2-benzothiazyl-n, n-dialkyldithiocarbamates |
US2912314A (en) * | 1956-05-01 | 1959-11-10 | Du Pont | Cracked fuel oils stabilized with amine salts of dithiocarbamic acids |
US5940247A (en) * | 1997-03-26 | 1999-08-17 | International Business Machines Corporation | Magnetic recording device with spindle motor lubricant of specified amine and carbamate concentrations/ratios |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2599350A (en) * | 1949-09-17 | 1952-06-03 | Standard Oil Dev Co | Oxidation inhibitor |
US3097168A (en) * | 1960-07-08 | 1963-07-09 | Dow Chemical Co | Gelling hydrocarbon liquids |
-
1943
- 1943-10-30 US US508381A patent/US2368106A/en not_active Expired - Lifetime
- 1943-11-12 US US510037A patent/US2385964A/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2785129A (en) * | 1951-07-03 | 1957-03-12 | Texas Co | Lubricating compositions containing 2-benzothiazyl-n, n-dialkyldithiocarbamates |
US2765277A (en) * | 1951-11-21 | 1956-10-02 | Exxon Research Engineering Co | Lubricating oil additives |
US2912314A (en) * | 1956-05-01 | 1959-11-10 | Du Pont | Cracked fuel oils stabilized with amine salts of dithiocarbamic acids |
US5940247A (en) * | 1997-03-26 | 1999-08-17 | International Business Machines Corporation | Magnetic recording device with spindle motor lubricant of specified amine and carbamate concentrations/ratios |
Also Published As
Publication number | Publication date |
---|---|
US2368106A (en) | 1945-01-30 |
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