Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Mixing of two or more solid polymers; mixing of solid...
Reexamination Certificate
1999-09-30
2002-01-15
Zitomer, Fred (Department: 1713)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Mixing of two or more solid polymers; mixing of solid...
C427S385500, C525S374000, C525S382000, C525S410000, C525S417000, C526S269000, C526S270000, C526S314000
Reexamination Certificate
active
06339129
ABSTRACT:
BACKGROUND OF THE INVENTION
Polymers containing the 5-membered cyclic carbonate functionality may be obtained via a number of methods. A recent review (
Polymer News,
23(6), 187-192 (1998)) summarizes many of the methods that have been reported in the literature of the synthesis of cyclic carbonate functional polymers and oligomers.
Seisan Kenkyu,
25 (7), (1973), describes the synthesis of the homopolymer of vinyl ethylene carbonate and copolymers of vinyl ethylene carbonate with styrene, vinyl acetate, and maleic anhydride. The only vinyl ester comonomer described is vinyl acetate. Copolymerizations were conducted in bulk to low conversion and solubility of the copolymers made was not discussed. This article also describes an attempt to crosslink a vinyl ethylene carbonate containing copolymer with ethylene diamine. This attempt was unsuccessful.
Plasticheskie Massy
, No. 2, 1996, 19-22 describes copolymerization of vinyl ethylene carbonate with methyl methacrylate, ethyl acrylate, and styrene. Yields of the copolymers were low and decreased as the level of vinyl ethylene carbonate was increased. The highest level of vinyl ethylene carbonate incorporated into a copolymer was 31.98 mole percent. This study did not include the copolymerization of vinyl ethylene carbonate with any vinyl ester monomers.
U.S. Pat. No. 5,567,527 describes the formation of coatings by copolymerization of vinyl ethylene carbonate with other comonomers and then crosslinking with multifunctional primary amines.
ACS Symposium Series 704 (Functional Polymers), 303-320 (1998) describes copolymerization experiments with vinyl ethylene carbonate and other unsaturated monomers. Copolymers of vinyl ethylene carbonate with vinyl acetate were incompatible with the solvent at vinyl ethylene carbonate contents of 40 percent and higher.
Cyclic carbonate functional acrylic copolymers may be prepared from the copolymerization of the acrylate and methacrylate esters of glycerin carbonate with other unsaturated monomers and are described for example in U.S. Pat. No. 2,979,514.
U.S. Pat. No. 5,726,251 discloses the use of certain amine carbamate salts as crosslinkers for epoxy resins in powder coatings. The amine carbamate salts are made by the reaction of a polyfunctional amine with carbon dioxide. Amine carbamate salts suitable for this application are solids and are stable toward water absorption and decomposition. The amine carbamate salts are blended with a solid epoxide functional resin using either melt extrusion or supercritical carbon dioxide. Upon coating the resulting powder on a substrate and heating, the powder melts and flows, the carbon dioxide is liberated from the amine carbamate salt, and the resulting amine reacts with the epoxy functional resin effecting cure. This patent only teaches the use of an epoxy functional resin with the amine carbamate salt. It also only discloses the use of difunctional amines as amine carbamate salt crosslinkers.
BRIEF SUMMARY OF THE INVENTION
The present invention describes the formation of cyclic carbonate functional polymer compositions by reaction of ethylenically unsaturated cyclic carbonate functional monomers and at least one other comonomer compatible with cyclic carbonate functional monomers. The resulting polymer compositions may be reacted with amine carbamate salts to form curable powder coating compositions.
DETAILED DESCRIPTION OF THE INVENTION
Cyclic carbonate polymer compositions of the present invention may be formed by reaction of ethylenically unsaturated cyclic carbonate functional monomers and at least one other comonomer compatible with cyclic carbonate functional monomers.
Vinyl ethylene carbonate is a preferred ethylenically unsaturated cyclic carbonate functional monomer for free radical copolymerization to form cyclic carbonate polymers. The homopolymer of vinyl ethylene carbonate may also be prepared by free radical polymerization. This polymer, however, has a low molecular weight and is soluble in only dipolar aprotic solvents, such as N-methyl pyrrolidinone, N,N-dimethyl acetamide, N,N-dimethyl formamide, dimethyl sulfoxide, and the like. These type solvents may be undesirable in a number of coating applications due to their toxicity and generally slow evaporation rate from a coating film. For use in powder coatings, the polymer must also be freed from solvents by either precipitation or extrusion.
In addition, the homopolymer of vinyl ethylene carbonate has poor compatibility with other resins or materials containing functional groups that would react with the cyclic carbonate groups for the formation of a cured thermosetting coating. This incompatibility may lead to incomplete reaction of the cyclic carbonate groups and the groups on the other resin and result in a coating with poor performance.
Vinyl ethylene carbonate may however be copolymerized with other ethylenically unsaturated monomers to form useful polymer compositions of the present invention. Preferred compositions include those containing from about 20 to about 50 percent vinyl ethylene carbonated reacted with at least one other comonomer.
Other monomers which may be used in copolymerizations with vinyl ethylene carbonate include, but are not limited to, the following:
(i) acrylic, methacrylic, crotonic or other unsaturated acids and their esters. These esters include methyl acrylate, ethyl acrylate, propyl acrylate, methyl methacrylate, butyl acrylate, butyl methacrylate, 2-ethyl hexyl acrylate, 2-ethyl hexyl methacrylate, hydroxy ethyl acrylate, hydroxy ethyl methacrylate, and the like;
(ii) Styrene-type monomers such as styrene, alpha-methyl styrene, vinyl toluene, and the like;
(iii) vinyl ester monomers such as vinyl acetate, vinyl propanoate, vinyl butyrate, vinyl 2-ethyl hexanoate, vinyl neononanoate, vinyl pivalate, vinyl neodecanoate, vinyl neoundecanoate, and the like;
(iv) allyl compounds which include allyl alcohol, allyl acetate, allyl chloride, and the like;
(v) other copolymerizable unsaturated monomers such as dimethyl maleate, dimethyl itaconate, diethyl maleate, dioctyl maleate, vinyl chloride, ethylene, acrylonitrile, acrylamide, and the like.
When copolymerized with esters of acrylic acid, esters of methacrylic acid or styrene, complete incorporation of vinyl ethylene carbonate into the copolymer is not achieved. By freeing the cyclic carbonate copolymer formed from the solvent by either precipitation or extrusion, any unreacted vinyl ethylene carbonate would also be removed. Thus, the fact that vinyl ethylene carbonate is not completely incorporated into a copolymer with methacrylic or acrylic monomers is not a significant barrier to use in powder coating applications.
More than one other comonomer may be used with vinyl ethylene carbonate in the copolymerization to yield the desired performance properties.
Particularly preferred polymer compositions are copolymers of vinyl ethylene carbonate with vinyl neononanoate, where vinyl ethylene carbonate is present in an amount from about 20 to about 50 weight percent.
Preferred compositions are those containing at least two cyclic carbonate groups per molecule, having a glass transition temperature of 40° C., and those compatible with the crosslinker.
The copolymerization of vinyl ethylene carbonate with vinyl ester monomers may be effected by any process used for free radical copolymerization including bulk, solution, emulsion, and suspension polymerization. A preferred process of the present invention involves gradual or incremental addition of a mixture of monomers simultaneously with the initiator to a vessel containing preheated solvent.
The choice of free radical initiator depends on the reaction conditions desired for the copolymerization. The polymerization may be initiated by conventional free radical initiators such as benzoyl peroxide, di-t-butyl peroxide, t-butyl peroctoate, t-amyl peroxy-2-ethyl hexanoate, t-butyl peroxy-2-ethyl hexanoate, hydrogen peroxide, dicumyl peroxide, t-butyl hydroperoxide, potassium or ammonium peroxydisulfate, 2,2′-azobis(2-methylpropanenitrile), 2,2′-azobis(
Boshears B. J.
Eastman Chemical Company
Graves, Jr. Bernard J.
Zitomer Fred
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