US2671760A - Lubricating oil compositions - Google Patents

Lubricating oil compositions Download PDF

Info

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
Application number
US227096A
Inventor
William S Port
Swern Daniel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US227096A priority Critical patent/US2671760A/en
Application granted granted Critical
Publication of US2671760A publication Critical patent/US2671760A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/04Macromolecular 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/06Macromolecular 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/06Macromolecular 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
    • C10M2209/062Vinyl esters of saturated carboxylic or carbonic acids, e.g. vinyl acetate
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular 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
    • C10M2209/082Macromolecular 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.
US227096A 1951-05-18 1951-05-18 Lubricating oil compositions Expired - Lifetime US2671760A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Patent Citations (5)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
US2655479A (en) Polyester pour depressants
US3996180A (en) High shear mixing of latex polymers
US3816314A (en) Block copolymers of unsaturated ester and a nitrogen containing monomer as v.i.improving and dispersant additives for oils
US2604453A (en) New copolymer compositions
US3951929A (en) Polyacrylates and waxy residual fuel compositions thereof
KR890002251A (en) Acrylic acid type viscosity giving agent without solvent and its manufacturing method
US4970260A (en) Novel viscosifiers for salt-containing solutions based on polymer complexes
KR950005856A (en) Solid Sheared Polymer Mixtures and Their Production Processes
US4756843A (en) Copolymer compositions usable as additives for lubricating oils
RU1788957C (en) Method of grafted copolymer preparation
US4496691A (en) Additives for lubricating oils containing styrene and heavy C12 -C.sub.
US2746925A (en) Lubricants and additives therefor
EP0439254A2 (en) Dispersant polymethacrylate viscosity index improvers
US3856685A (en) Lubricant compositions
US2671760A (en) Lubricating oil compositions
DE2216590C3 (en) Process for the preparation of copolymers from olefins and acrylic acid compounds
FI83090C (en) FOERFARANDE FOER BILDANDE AV EN LOESNING AV EN VATTEN LOESLIG POLYMER, VILKEN INNEHAOLLER SURA GRUPPER, I EN BLANDNING AV ETT POLART LOESNINGSMEDEL, VATTEN OCH BAS.
US3394115A (en) Trifluoroethoxyethyl acrylate and polymers thereof
CA1079444A (en) N-substituted acrylamidine copolymers of n-substituted acrylamidines and esters of acrylic and methacrylic acid and uses of the copolymers
Port et al. Viscosity Index Improvers for Lubricating Oils. Polyvinyl Esters ofLong-Chain Fatty Acids.
US2944974A (en) Lubricating oil compositions
Ronel et al. Terpolymerization studies. I. Terpolymerization of acrylonitrile, styrene, and esters of α‐cyanocinnamic acid
US2430993A (en) Plasticizing polyisobutylene utilizing benzoyl peroxide
US2615864A (en) Esterified allyl ester-polycarboxylic acid copolymers
US3718591A (en) Lubricant compositions containing terpolymers