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Publication numberUS3159608 A
Publication typeGrant
Publication dateDec 1, 1964
Filing dateJan 8, 1963
Priority dateJan 8, 1963
Publication numberUS 3159608 A, US 3159608A, US-A-3159608, US3159608 A, US3159608A
InventorsIlnyckyj Stephan
Original AssigneeExxon Research Engineering Co
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Copolymerization of ethylene and vinyl acetate
US 3159608 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

United States Patent 3,159,608 COPOLYMERIZATION 0F ETHYLENE AND VINY L ACETATE Stephan llnycliyj, Sarnia, Ontario, Canada, assignor to Esso Research and Engineering Company, a corporation of Delaware No Drawing. Filed Jan. 8, 1963, Ser. No. 249,989 3 Claims. (Cl. 260-873) The present invention relates to the manufacture of pour depressants, particularly for use with middle distillates. The pour depressant of the present invention comprises copolymers of ethylene with up to about 50% by weight of an olefinically unsaturated aliphatic monomer containing from about 3 to 5 carbon atoms per molecule. The copolymers of a particular average molecular weight are obtained by controlling the conditions of reaction. The preferred copolymer of the present invention is a panticular copolymer of ethylene and vinyl acetate. Pour depressants of improved potency and at a higher yield relative to amount of peroxide employed are secured by utilizing a benzene solvent containing a critical quantity of toluene.

The present application is a continuation-in-part of Serial No. 1,838, filed January 5, 1960, entitled Process for the Manufacture of Improved Pour Depressants for Middle Distillates, inventor: Stephan Ilnyckyj.

With the increase in the use of hydrocarbon fuels of all kinds, a serious problem has arisen in areas frequently subjected to low temperatures in the cold test characteristics of fuels. Particularly, serious problems have been encountered with heating oils and diesel and jet fuels that have too high a pour point, resulting either in distributional or operating difiicul ties or both. For eX- ample, the distribution of heating oils by pumping or syphoning is rendered difiicult or impossible at temperatures around or below the pour point of the oil. Furthermore, the flow of the oil at such temperatures through the filters cannot be maintained, leading to the failure of the equipment to operate.

Also, the low temperature properties of petroleum distillate fuels boiling in the range between about 250 and about 750 F. have attracted increasing attention in recent years because of the growth of market for such fuels in subarctic areas and because of the development of turbo-jet aircraft capable of operating at altitudes where temperatures of 50 F. or lower may be encountered.

It is, therefore, an object of the present invention to set forth an improved process for the manufacture of very elfective pour depressants for middle distillates and lighter oils. In general, these oils boil in the range from about 250 to 750 F.

It is a still further object of the present invention to provide heating oils, diesel fuel oils, kerosines and jet fuels having low pour points. Aviation turbo-jet fuels in which the polymers may be used normally boil between about 250 and about 550 F. and are used in both military and civilian aircraft. Such fuels are more fully defined by US. Military Specifications MIL-F-5624C, MILF25554A, MlI .--'l-"25558A, and amendments thereto. Kerosines and heating oils will normally have boiling ranges between about 300 and about 750 F. and are more fully described in ASTM Specification D- 396-48T and supplements thereto, Where they are re- 3,159,608 Patented Dec. 1, 1964 ferred to as No. 1 and No. 2 fuel oils. Diesel fuels in which the polymers may be employed are described in detail in ASTM Specification D-975-53T and later versions of the same specification.

The process of the present invention produces copolymers of ethylene and up to about 50% by weight of an olefinically unsaturated aliphatic monomer containing from about 3 to 5 carbon atoms per molecule. In general, these compounds may comprise vinyl acetate, vinyl propionate, methyl methacrylate, allyl ethyl ether, divinyl ether, acrylonitrile, vinylacetonitrile and the like.

The preferred copolymers comprise ethylene-vinyl acetate copolymer. It is preferred that the parts by by weight of ethylene in the copolymer be in the range from about 60 to 99% as compared to parts by weight of vinyl acetate in the range from about 40 to about 1%. A very desirable ethylene vinyl acetate copolymer contains about 15 to 28% by weight of vinyl acetate as, for example, about 20 parts by weight of vinyl acetate.

The molecular weights of the ethylene-vinyl acetate copolymer are critical and should be in the range from about 1,000 to 3,000, preferably in the range from about 1,500 to 2,200. The molecular weights are determined by K. Rasts method (Ber. 55, 1051, 3727 (1922)).

The ethylene-vinyl acetate copolymer as described above is used in a concentration in the range from about .001 to 0.2% by weight, preferably in a concentration in the range from about .005 to .1% by weight.

In accordance with the present invention, the polymerization process is conducted in a benzene solvent having added thereto a critical quantity of toluene. The initiator comprises any peroxy compound, preferably ditertiary-butylperoxide. The temperature of the polymerization reaction is in the range from about 280 to 340 F. A very desirable temperature is about 300 F. The pressure is in the range from about 1000 pounds to 5000 pounds, preferably in the range from about 1200 to 3000 pounds. The amount of toluene present is in the range from 1% to 30% by volume, preferably in the range from about 5 to 20% by volume based upon the quantity of benzene present.

The autoclave or similar equipment containing the solvent, initiator and vinyl acetate is purged with nitrogen, then with ethylene before charging with a suificient amount of ethylene to yield the desired pressure when heated to the reaction temperature. During the polymerization, additional ethylene is added to maintain the pressure at the desired level. Polymerization is considered complete when the pressure drops less than 50 p.s.i.g. per hour. The product is stripped free of solvent and unreacted vinyl acetate under vacuum.

A number of operations were carried out wherein copolymers were produced under different pressures and other varying conditions. These copolymers were then tested as pour depressants in a blend of virgin gas oil and a catalytically cracked gas oil having an ASTM pour of +20 F. The virgin gas oil boiled in :the range from about 350 to 700 F., and the cracked gas oil boiled in the range from about 350 to 650 -F. As pointed out heretofore, the critical factors with respect to producing desirable polymers are the molecular weights and the concentration of the vinyl acetate in the polymer. The results of these tests are shown in the following Table I.

3 Table I [Oonditionsz Temperature 300 F., total time 3% hours. Vinyl acetate 300 mls. over 3 hours, di-t-butyl peroxide 30 mls. over 3% hours] Operation A B C D Conditions:

Pressure, p.s.i.g 900 1, 200 1,200 1, 200 Benzene, mls 1, 800 1, 800 1, 710 1, 440 Toluene, mls nil nil 90 360 Product:

Yield, g 731 970 870 753 Oopolymer, gm/Peroxide, g 30. 7 40. 8 36.6 31. Yield and Efiiciency, Increase,

Percent 36. 0 19. 4 3. 0 Vinyl Acetate, wt. percent 30. 4 23. 7 24. 0 26. 4 Molecular Weight 1 1, 800 3, 170 2, 780 1, 800 Viscosity at 100 F., 08."... 318 995 345 102 Pour Depression, F.:

With 0.015 wt. percent 55 25 50 With 0.026 wt. percent 75 56 65 85 1 By cryoscopy in phenanthrene. 2 50/60 copolymer/kerosene solution. 3 In Reference Oil, ASTM Pour +25 F.

From the above it is apparent that in Operation A with :a pressure at 900 pounds, a very satisfactory pour depressant was secured. This depressant had a molecular weight of about 1800 and a satisfactory viscosity of 318.

On the other hand, in Operation B, the yield was greatly increased. However, the product had a molecular weight of about 3170 and a viscosity which is not at all satisfactory. Furthermore, the potency of the product was not satisfactory.

In Operation C and D conducted at 1200 pounds, in the presence of relatively minor quantities of toluene, the yields were appreciably increased and the viscosities excellent. Furthermore, the potency of the resulting products were very great. The increased yield obtained in Operation C indicates that there is an optimum concentration of toluene in benzene for any given conditions.

This optimum concentration is determined by pressure and desired composition of copolymer.

What is claimed is:

1. Process for the manufacture of a pour depressant comprising a copolymer of ethylene and vinyl acetate which comprises introducing ethylene into a reaction zone containing a peroxy compound and a benzene solvent to which has been added from about 130% by volume of toluene, thereafter raising the temperature of said reaction zone to a temperature in the range from 280 to 340 F. and to a pressure in the range from 1000 to 5000 pounds per sq. in., thereafter adding to said reaction zone vinyl acetate and suflicient ethylene to maintain the pressure in said range, carrying out said reaction at a temperature in the range from 280 to 340 F. for a period of from 2 to 16 hours under conditions wherein the concentration of the vinyl acetate in the benzene solution varies from about 0.2 to 10.0%, whereby a polymer having a molecular weight in the range from about 1000 to 3000 is secured, wherein the concentration of the vinyl acetate in the product will vary from about 15 to 28% by weight.

2. Process as defined by claim 1 wherein the amount of toluene present is in the range from about 5 to 20% by volume as compared to the benzene present.

3. The process as defined by claim 1 wherein said peroxy compound is di-ter'tiary-butyl-peroxide.

OTHER REFERENCES Mellan: Industrial Solvents, page 272, Reinhold 1950).

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2396785 *Mar 15, 1941Mar 19, 1946Du PontProcess for polymerizing olefins with other polymerizable organic compounds
US3093623 *Jan 5, 1960Jun 11, 1963Exxon Research Engineering CoProcess for the manufacture of improved pour depressants for middle distillates
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3344129 *May 26, 1964Sep 26, 1967Hoechst AgProcess of hydrolyzing vinyl ester-ethylene copolymers
US3367896 *Sep 29, 1964Feb 6, 1968Allied ChemScuff resistant inks comprising drying oil and ethylene-vinyl acetate copolymer
US3522041 *Jan 19, 1967Jul 28, 1970Addressograph MultigraphPhotoelectrostatic recording member
US4076679 *Jan 21, 1977Feb 28, 1978The Dow Chemical CompanyRapid setting polyurethane elastomers and process of preparation
US4417038 *Dec 4, 1981Nov 22, 1983Basf AktiengesellschaftEthylene-alkyne copolymers, their preparation and their use as additives to petroleum distillates
US4497941 *Sep 30, 1982Feb 5, 1985Exxon Research & Engineering Co.Ethylene copolymers for hot melt systems
US4559155 *Mar 12, 1985Dec 17, 1985The Lubrizol CorporationHydrocarbyl substituted carboxylic acylating agent derivative containing combinations, and fuels containing same
US4564460 *Aug 9, 1982Jan 14, 1986The Lubrizol CorporationHydrocarbyl-substituted carboxylic acylating agent derivative containing combinations, and fuels containing same
US4575526 *Mar 12, 1985Mar 11, 1986The Lubrizol CorporationHydrocarbyl substituted carboxylic acylaging agent derivative containing combinations, and fuels containing same
US4613342 *Oct 16, 1985Sep 23, 1986The Lubrizol CorporationHydrocarbyl substituted carboxylic acylating agent derivative containing combinations, and fuels containing same
US4649186 *Jul 1, 1985Mar 10, 1987Eastman Kodak CompanyProcess for preparing copolymers of ethylene and vinyl acetate
US5200484 *Jun 18, 1991Apr 6, 1993Hoechst AktiengesellschaftVinyl acetate and isobutyl vinyl ether
US6099601 *Feb 20, 1997Aug 8, 2000Basf AktiengesellschaftEthylene-vinyl formate copolymers, process for their preparation, their use as flow improvers, and fuel and propellant compositions comprising them
US6235069 *May 24, 2000May 22, 2001Basf AktiengesellschaftEthylene-vinyl formate copolymers, process for their preparation, their use as flow improvers, and fuel and propellant compositions comprising them
DE1570528A1 *Dec 10, 1965Mar 5, 1970Exxon Research Engineering CoVerfahren zur Herstellung von Stockpunktsdepressoren
DE1914756A1 *Mar 22, 1969Nov 6, 1969Exxon Research Engineering CoVerfahren zur Herstellung von Mischpolymerisaten sowie deren Verwendung in Destillatoelen
DE2515805A1 *Apr 11, 1975Oct 30, 1975Exxon Research Engineering CoAethylencopolymere, verfahren zu deren herstellung und dieselben enthaltende destillatoele
Classifications
U.S. Classification526/227, 526/87, 526/331
International ClassificationC08F10/00
Cooperative ClassificationC08F10/00
European ClassificationC08F10/00