US2671760A - Lubricating oil compositions - Google Patents
Lubricating oil compositions Download PDFInfo
- Publication number
- US2671760A US2671760A US227096A US22709651A US2671760A US 2671760 A US2671760 A US 2671760A US 227096 A US227096 A US 227096A US 22709651 A US22709651 A US 22709651A US 2671760 A US2671760 A US 2671760A
- Authority
- US
- United States
- Prior art keywords
- lubricating oil
- polymer
- copolymer
- lubricating
- palmitate
- 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 claims description 24
- 239000000203 mixture Substances 0.000 title claims description 13
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 9
- UJRIYYLGNDXVTA-UHFFFAOYSA-N ethenyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC=C UJRIYYLGNDXVTA-UHFFFAOYSA-N 0.000 claims description 7
- 229920000140 heteropolymer Polymers 0.000 claims description 4
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 description 21
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 229920000642 polymer Polymers 0.000 description 18
- 239000000178 monomer Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 10
- 239000000654 additive Substances 0.000 description 6
- 238000007334 copolymerization reaction Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000004342 Benzoyl peroxide Substances 0.000 description 5
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
- 235000019400 benzoyl peroxide Nutrition 0.000 description 5
- 229920001519 homopolymer Polymers 0.000 description 5
- 239000003921 oil Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- YQAHABBBFVAGBK-UHFFFAOYSA-N acetic acid;hexadecanoic acid Chemical compound CC(O)=O.CCCCCCCCCCCCCCCC(O)=O YQAHABBBFVAGBK-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000007614 solvation Methods 0.000 description 2
- 239000002199 base oil Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000012674 dispersion polymerization Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/04—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/06—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/06—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
- C10M2209/062—Vinyl esters of saturated carboxylic or carbonic acids, e.g. vinyl acetate
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/082—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type monocarboxylic
Definitions
- This invention relates to lubricating compositions and particularly to the improvement of lubricating oil compositions by the incorporation therein of copolymeric additives which improve their viscosity index.
- the viscosity of a high polymer solution depends on the size of the polymer, the extent of the intraand intermolecular. interaction of the sec. 266
- polymer molecules the extent of the interaction between the polymer molecules and the solvent, the concentration of the polymer and the nature of the solvent.
- a polymer having a high degree of polymerization because its higher molecular volume acts toimpede the liquid flow, gives a solution of higher viscosity than does a low molecular weight polymer. If the intramolecular forces are high and the. degree .of solvation is low (i. e. a poor solvent), the in temal attracting forces will cause the polymer molecules to curl up in compact form decreasing the effective volume and surface area of contact, giving solutions of low viscosity.
- a lubricating oil composition having an improved viscosity index may be obtained by incorporating in the lubricating oil a linear heteropolymer, particularly a copolymer, prepared by the copolymerization of I two or more monomers.
- a linear heteropolymer particularly a copolymer, prepared by the copolymerization of I two or more monomers.
- monomers used in preparing the heteropolymer are chosen in such a manner that one of them gives a homopolymer having high solubility in lubricating oils whereas the other gives a homo polymer. having substantially no solubility in lubricating oils.
- An example of suitable monomers are vinyl palmitate which gives a homopolymer quite soluble in lubricating oils and vinyl acetate which gives a homopolymer quite insoluble in lubricating oils.
- Monomers which give polymers having considerable solubility in lubricating oils may be chosen from the group of vinyl esters and ethers having from about 8 to 22 carbon atoms per molecule.
- polymers having molecular weights in the range of about 5,000 to 100,000 are most valuable for this purpose.
- This invention makes it possible .to provide an effective additive for lubricants substantially regardless of the solvent powers of the base stock. Hitherto only two methods were available for improving the viscosity index of lubricating oils to a significant degree. These were, first, the use of polymers having a very high degree of polymerization and, second, addition to the oil of insolubilizing agents which render the additive less soluble. The first of these methods is limited by several factors, of which an important one is the tendency of high molecular weight additives to shear and break down under stress. The second of these methods, the addition of insolubilizing agents is expensive and diflicult to control and therefore has not been used generally.
- Example 1 Polyvinyl palmitate A solution of 141.2 g. of vinyl palmitate and 0.605 g. of benzoyl peroxide in 97.5 g. of benzene was heated in a nitrogen atmosphere for 6.5 hours at 75 C. The solution was then diluted with 500 ml. of benzene and poured into 3 l. of acetone to precipitate the polymer. A 58% conversion was obtained.
- Example 2 Polyvinyl acetate palmitate A solution of 105 g. of vinyl palmitate, 95 g. of vinyl acetate and 1.78 g. of benzoyl peroxide in 288 g. of benzene was heated in a nitrogen atmosphere for 7 hours at 70-73 C. The resulting solution was poured into 2.6 l. of methanol to precipitate the copolymer. The yield of copolymer after a total of three precipitations was 66%. The copolymer contained about 75 mole percent of vinyl acetate.
- Example 3 Polyvinyl acetate palmitate A copolymer containing approximately 50 mole percent of vinyl acetate was prepared by heating a solution of 153.2 g. of vinyl palmitate, 46.8 g. of vinyl acetate and 1.31 g. of benzoyl peroxide in 210 g. of benzene, as described in .Example 2. The yield of copolymer after purification was 59%.
- Example 4 Polyvinyl acetate :palmitate A copolymer containing approximately 25 mole percent of vinyl acetate was prepared by heating a solution of 181.4 g. of vinyl palmitate, 18.6 g. of vinyl acetate and 1.04 g. of benzoyl peroxide in 168 g. of benzene, as described in Example 2. The yield of copolymer after purification was 60%.
- Example 5 Polyvznyl acetate :palmitate oleate Viscosity Index ol Treated and Untreated Lubricating Polymer Oils From Exam 4..-. From Example 3.--. From Example 2 I Calculated from tables of Dean and Davis [Chem. & Met. Eng 36, #10, 618 (1929)].
- the copolymerization temperature may be varied over wide limits. Temperatures much in excess of 75 C. often cause the copolymerizations to proceed too rapidly for effective control.
- the preferred operative temperatures are in the range of about 20 to C.
- the isolation of the copolymer can be efl'ected in a variety of known ways depending mainly on the copolymerization technique employed.
- the polymer may be isolated, if desired, by evaporation and recovery of solvent; alternatively, the copolymerization solution may be added directly to the petroleum base stock followed by removal of residual solvent in the usual ways.
- copolymers which are valuable for additives to lubricating oils may be prepared from monomer mixtures containing up to about 50 mol percent of the insolubilizing monomer. Below about 5 mol percent of the insolubilizing monomer we have not observed the desired effect on viscosity index. We prefer to employ copolymers prepared from mixed monomers containing between 25 mol percent and 50 mol percent of the insolubilizing monomer.
- a lubricating oil composition having an improved viscosity index comprising a'lubricating oil having incorporated therein a linear heteropolymer having a molecular weight of about from 5,000 to 100,000 and having been prepared by polymerizing a mixture containing, as polymerizable components, monomeric vinyl acetate and monomeric vinyl palmitate.
- a lubricating oil composition having an improved viscosity index comprising a lubricating -oil having incorporated therein a linear copoly- References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 2,020,703 Shumann et al. Nov. 12, 1935 2,020,714 Wuefi et al. Nov. 12, 1935 2,091,627 Bruson Aug. 31, 1937 2,104,408 Wiezevich Jan. 4, 1938- 2600385 Bauer et a1 June 17, 1952
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
I Patented 9, 1954 LUBRICATING on. COMPOSITIONS William s. Port, James w. O'Brien, and Daniel Swern, Philadelphia, Pa., assignors to the United States of America as represented by the Secretary of Agriculture No Drawing. ApplicationMay 1a, 1951,
Serial No. 227,090
3 Claims. (01. 252-56) (Granted under Title 35,)U. S. Code (1952),
The invention herein described may be manuiactured and used by or'for the Government of the United States of America for governmental purposes throughout the world without the payment to. us of any royalty thereon.
This invention relates to lubricating compositions and particularly to the improvement of lubricating oil compositions by the incorporation therein of copolymeric additives which improve their viscosity index.
In recent years, because of increased use of complex machines operating through wide temperature ranges, necessity has arisen for the ready availability of lubricating oils having improved viscosity-temperature characteristics. The ideal lubricant, of course, would show little or no viscosity change with temperature. Various attempts have been made to impart .improved' viscosity-temperature characteristics to lubricating oils. The improvement in viscosity index which can be obtained from increased refining g and from mixing of petroleum stocks is limited and, therefore, other methods must be used. It is accordingly an object of this invention to provide improvements .in the viscosity properties of lubricating oils and lubricating oil compositions.
The viscosity of a high polymer solution depends on the size of the polymer, the extent of the intraand intermolecular. interaction of the sec. 266
polymer molecules, the extent of the interaction between the polymer molecules and the solvent, the concentration of the polymer and the nature of the solvent. In general, a polymer having a high degree of polymerization, because its higher molecular volume acts toimpede the liquid flow, gives a solution of higher viscosity than does a low molecular weight polymer. If the intramolecular forces are high and the. degree .of solvation is low (i. e. a poor solvent), the in temal attracting forces will cause the polymer molecules to curl up in compact form decreasing the effective volume and surface area of contact, giving solutions of low viscosity.
In polymer solutions where the intraand intermolecular forces are low, and the solvation forces are high (i. e. a good solvent), each polymer molecule is sheathed by solvent mole= cules and tends to uncurl into long chains increasing the effective volume and the surface area of contact, giving solutions of higher viscosity than in a poor solvent.
According to the invention, a lubricating oil composition having an improved viscosity index may be obtained by incorporating in the lubricating oil a linear heteropolymer, particularly a copolymer, prepared by the copolymerization of I two or more monomers. We have discovered that it is possible to prepare ,copolymers having gradually changing solubility in any given lubricating oil by merely controlling the relative proportions of each of the monomers introduced into the polymer chain and that such copolymers are desirable additives for lubricating oils. The
monomers used in preparing the heteropolymer are chosen in such a manner that one of them gives a homopolymer having high solubility in lubricating oils whereas the other gives a homo polymer. having substantially no solubility in lubricating oils. An example of suitable monomers are vinyl palmitate which gives a homopolymer quite soluble in lubricating oils and vinyl acetate which gives a homopolymer quite insoluble in lubricating oils. Monomers which give polymers having considerable solubility in lubricating oils may be chosen from the group of vinyl esters and ethers having from about 8 to 22 carbon atoms per molecule. Monomers which givepolymers having substantially no solubilityin preparation of the copolymer to be added, it
is possible to control the solubility of the polymer in the base oil to a considerable degree. Co-
polymers having molecular weights in the range of about 5,000 to 100,000 are most valuable for this purpose. This invention makes it possible .to provide an effective additive for lubricants substantially regardless of the solvent powers of the base stock. Hitherto only two methods were available for improving the viscosity index of lubricating oils to a significant degree. These were, first, the use of polymers having a very high degree of polymerization and, second, addition to the oil of insolubilizing agents which render the additive less soluble. The first of these methods is limited by several factors, of which an important one is the tendency of high molecular weight additives to shear and break down under stress. The second of these methods, the addition of insolubilizing agents is expensive and diflicult to control and therefore has not been used generally.
The following examples are illustrative of the nature of our invention, but our invention is not restricted to these examples.
Example 1.-Polyvinyl palmitate A solution of 141.2 g. of vinyl palmitate and 0.605 g. of benzoyl peroxide in 97.5 g. of benzene was heated in a nitrogen atmosphere for 6.5 hours at 75 C. The solution was then diluted with 500 ml. of benzene and poured into 3 l. of acetone to precipitate the polymer. A 58% conversion was obtained.
Example 2.Polyvinyl acetate palmitate A solution of 105 g. of vinyl palmitate, 95 g. of vinyl acetate and 1.78 g. of benzoyl peroxide in 288 g. of benzene was heated in a nitrogen atmosphere for 7 hours at 70-73 C. The resulting solution was poured into 2.6 l. of methanol to precipitate the copolymer. The yield of copolymer after a total of three precipitations was 66%. The copolymer contained about 75 mole percent of vinyl acetate.
Example 3.Polyvinyl acetate palmitate A copolymer containing approximately 50 mole percent of vinyl acetate was prepared by heating a solution of 153.2 g. of vinyl palmitate, 46.8 g. of vinyl acetate and 1.31 g. of benzoyl peroxide in 210 g. of benzene, as described in .Example 2. The yield of copolymer after purification was 59%.
Example 4Polyvinyl acetate :palmitate A copolymer containing approximately 25 mole percent of vinyl acetate was prepared by heating a solution of 181.4 g. of vinyl palmitate, 18.6 g. of vinyl acetate and 1.04 g. of benzoyl peroxide in 168 g. of benzene, as described in Example 2. The yield of copolymer after purification was 60%.
Example 5.Polyvznyl acetate :palmitate oleate Viscosity Index ol Treated and Untreated Lubricating Polymer Oils From Exam 4..-. From Example 3.--. From Example 2 I Calculated from tables of Dean and Davis [Chem. & Met. Eng 36, #10, 618 (1929)].
It is evident that the improvement in viscosity index obtained by copolymers is significantly greater than that obtained by addition of a homopolymer (from Example 1). It is also obvious that the copolymer from Examples 2 and 3 tends to be superior to that from Example 4 for oil A whereas the copolymer from Example 4 would be preferred over that of Example 3 for addition to oil 13.
Although the examples given above describe the copolymerization of the mixed monomers in benzene solution using benzoyl peroxide as a catalyst, we have found that equally valuable products can be prepared by bulk, emulsion, reductive-activation or dispersion polymerization techniques. Other solvents and chain transfer agents may also be employed and other peroxide. or free radical type catalysts may be used.
The copolymerization temperature may be varied over wide limits. Temperatures much in excess of 75 C. often cause the copolymerizations to proceed too rapidly for effective control. The preferred operative temperatures are in the range of about 20 to C.
The isolation of the copolymer can be efl'ected in a variety of known ways depending mainly on the copolymerization technique employed. When solution polymerization is employed, the polymer may be isolated, if desired, by evaporation and recovery of solvent; alternatively, the copolymerization solution may be added directly to the petroleum base stock followed by removal of residual solvent in the usual ways.
We have found that the copolymers which are valuable for additives to lubricating oils may be prepared from monomer mixtures containing up to about 50 mol percent of the insolubilizing monomer. Below about 5 mol percent of the insolubilizing monomer we have not observed the desired effect on viscosity index. We prefer to employ copolymers prepared from mixed monomers containing between 25 mol percent and 50 mol percent of the insolubilizing monomer.
We have found that the operable range of copolymer concentration in the lubricating oil is somewhat dependent upon the solvent power of the petroleum base stock as well as upon the specific composition of the copolymer being used. We prefer to add the copolymers in amounts varying from about 1% to about 10% of the base stock.
We claim:
1. A lubricating oil composition having an improved viscosity index comprising a'lubricating oil having incorporated therein a linear heteropolymer having a molecular weight of about from 5,000 to 100,000 and having been prepared by polymerizing a mixture containing, as polymerizable components, monomeric vinyl acetate and monomeric vinyl palmitate.
2. A lubricating oil composition having an improved viscosity index comprising a lubricating -oil having incorporated therein a linear copoly- References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 2,020,703 Shumann et al. Nov. 12, 1935 2,020,714 Wuefi et al. Nov. 12, 1935 2,091,627 Bruson Aug. 31, 1937 2,104,408 Wiezevich Jan. 4, 1938- 2600385 Bauer et a1 June 17, 1952
Claims (1)
1. A LUBRICATING OIL COMPOSITION HAVING AN IMPROVED VISCOSITY INDEX COMPRISING A LUBRICATING OIL HAVING INCORPORATED THEREIN A LINEAR HETEROPOLYMER HAVING A MOLECULAR WEIGHT OF ABOUT FROM 5,000 TO 100,000 AND HAVING BEEN PREPARED BY POLYMERIZING A MIXTURE CONTAINING, AS POLYMERIZABLE COMPONENTS, MONOMERIC VINYL ACETATE AND MONOMERIC VINYL PALMITATE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US227096A US2671760A (en) | 1951-05-18 | 1951-05-18 | Lubricating oil compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US227096A US2671760A (en) | 1951-05-18 | 1951-05-18 | Lubricating oil compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2671760A true US2671760A (en) | 1954-03-09 |
Family
ID=22851730
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US227096A Expired - Lifetime US2671760A (en) | 1951-05-18 | 1951-05-18 | Lubricating oil compositions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2671760A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3052623A (en) * | 1960-04-29 | 1962-09-04 | Socony Mobil Oil Co Inc | Process for dewaxing of lube oils and deoiling of waxes |
| US3344100A (en) * | 1965-07-28 | 1967-09-26 | Goodrich Co B F | Emulsion polymerization using water insoluble metal salts of fatty acids |
| US3390089A (en) * | 1961-11-30 | 1968-06-25 | Exxon Research Engineering Co | Lubricating oil containing polymeric additive |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2020714A (en) * | 1932-10-12 | 1935-11-12 | Ig Farbenindustrie Ag | Lubricating hydrocarbon product |
| US2020703A (en) * | 1932-10-11 | 1935-11-12 | Ig Farbenindustrie Ag | Improved hydrocarbon products, especially lubricating oils |
| US2091627A (en) * | 1934-06-08 | 1937-08-31 | Rohm & Haas | Composition of matter and process |
| US2104408A (en) * | 1933-09-20 | 1938-01-04 | Standard Oil Dev Co | Lubricant |
| US2600385A (en) * | 1950-05-12 | 1952-06-17 | Rohm & Haas | Vinyl ester copolymers |
-
1951
- 1951-05-18 US US227096A patent/US2671760A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2020703A (en) * | 1932-10-11 | 1935-11-12 | Ig Farbenindustrie Ag | Improved hydrocarbon products, especially lubricating oils |
| US2020714A (en) * | 1932-10-12 | 1935-11-12 | Ig Farbenindustrie Ag | Lubricating hydrocarbon product |
| US2104408A (en) * | 1933-09-20 | 1938-01-04 | Standard Oil Dev Co | Lubricant |
| US2091627A (en) * | 1934-06-08 | 1937-08-31 | Rohm & Haas | Composition of matter and process |
| US2600385A (en) * | 1950-05-12 | 1952-06-17 | Rohm & Haas | Vinyl ester copolymers |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3052623A (en) * | 1960-04-29 | 1962-09-04 | Socony Mobil Oil Co Inc | Process for dewaxing of lube oils and deoiling of waxes |
| US3390089A (en) * | 1961-11-30 | 1968-06-25 | Exxon Research Engineering Co | Lubricating oil containing polymeric additive |
| US3344100A (en) * | 1965-07-28 | 1967-09-26 | Goodrich Co B F | Emulsion polymerization using water insoluble metal salts of fatty acids |
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