Patent US4076921A successfully refreshed from Google Patents.
US4076921A
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US
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Method of producing glycol methacrylate or glycol acrylate polymers and copolymers
Assignee: Czech Academy of Sciences
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Filing: 1972-10-13
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Granted: 1978-02-28
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Expires: 1992-10-13
Abstract
Abstract A starting monomer mixture containing a minor amount of a cross linking agent is precipitation polymerized in a diluent/precipitant which is an unlimited solvent for the starting monomers but is neither a solvent nor a substantial swelling agent for the resultant polymer. The resultant product falling from the polymerization contains soluble and insoluble hydrophilic polymers and copolymers.
Inventors
- 👤 Miroslav Stol
- 👤 Vladimir Stoy
- 👤 Zdenek Tuzar
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-23 14:21
CPC Classifications
C; C08; C08F; C08F220/00; C08F220/02; C08F220/10; C08F220/26; C08F220/28; C08F220/282; Y; Y10; Y10S; Y10S526/00; Y10S526/93
Claims Analysis
Total Claims: 11
Claim 1
Independent Claim
313 words
The method of producing hydrophilic polymer products comprising a mixture of both soluble and insoluble components which comprises forming a starting monomer mixture consisting essentially of (1) a major portion of monoesters of methacrylic and/or acrylic acids and polyvalent alcohols selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propylene glycol, 1,4-butylene glycol, glycerol, pentaerythritol, mannitol and sorbitol, and (2) a minor amount of a crosslinking agent selected from the group consisting of di- and triesters of methacrylic and/or acrylic acid and polyvalent alcohols selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propylene glycol, 1,4-butylene glycol, glycerol, pentaerythritol, mannitol and sorbitol; combining said starting monomer mixture with (3) a member selected from the group consisting of monocyclic and bicyclic aromatic and partly hydrogenated monocyclic and bicyclic aromatic hydrocarbons, halogenated aliphatic and cycloaliphatic hydrocarbons, esters of carboxylic acids and aliphatic and aromatic alcohols, ethers, cycloethers, ketones and cycloketones, said last mentioned group member being capable of unlimitedly dissolving all of the monomer components but being a nonsolvent and/or swelling agent for the polymer product, said monomer being present in an amount of less than 66% by weight of the total polymerization mixture including said last mentioned group member; polymerizing said monomer mixture under conditions of free radical polymerization to form a polymeric product which is in part soluble and in part insoluble in a member selected from the group consisting of lower aliphatic alcohols, dimethylformamide, glycol methacrylate and glycol acrylate; and effecting the combination of the monomer mixture with the group (3) member during such polymerization in small quantities under controlled stirring at a rate at which the polymeric product formed separates out of the polymerization solution and at which the concentration of the crosslinking agent is maintained within the critical range of 0.02 to 0.2% by volume based on the total volume of the polymerization mixture.
Claim 2
Independent Claim
313 words
The method of producing hydrophilic polymer products comprising a mixture of both soluble and insoluble components which comprises forming a starting monomer mixture consisting essentially of (1) a major portion of monoesters of methacrylic and/or acrylic acids and polyvalent alcohols selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propylene glycol, 1,4-butylene glycol, glycerol, pentaerythritol, mannitol and sorbitol, and (2) a minor amount of a crosslinking agent selected from the group consisting of di- and triesters of methacrylic and/or acrylic acid and polyvalent alcohols selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propylene glycol, 1,4-butylene glycol, glycerol, pentaerythritol, mannitol and sorbitol; combining said starting monomer mixture with (3) a member selected from the group consisting of monocyclic and bicyclic aromatic and partly hydrogenated monocyclic and bicyclic aromatic hydrocarbons, halogenated aliphatic and cycloaliphatic hydrocarbons, esters of carboxylic acids and aliphatic and aromatic alcohols, ethers, cycloethers, ketones and cycloketones, said last mentioned group member being capable of unlimitedly dissolving all of the monomer components but being a nonsolvent and/or swelling agent for the polymer product, said monomer being present in an amount of less than 66% by weight of the total polymerization mixture including said last mentioned group member; polymerizing said monomer mixture under conditions of free radical polymerization to form a polymeric product which is in part soluble and in part insoluble in a member selected from the group consisting of lower aliphatic alcohols, dimethylformamide, glycol methacrylate and glycol acrylate; and effecting the combination of the monomer mixture with the group (3) member during such polymerization in small quantities under controlled stirring at a rate at which the polymeric product formed separates out of the polymerization solution and at which the concentration of the crosslinking agent is maintained within the critical range of 0.02 to 0.2% by volume based on the total volume of the polymerization mixture.
Claim 3
Dependent Claim
53 words
The method according to claim 1 wherein said monomer group member (1) is introduced at a rate adapted to the amount of crosslinking agent and is held above a limit where crosslinked polymer is formed but under a limit where the content of said crosslinked polymer exceeds 90 wt.% of the polymer product.
Claim 4
Dependent Claim
18 words
The method according to claim 1 wherein said polymer product has a grain size of about 1 μ.
Claim 5
Dependent Claim
40 words
The method according to claim 1 wherein said monomer (1) is in part replaced by a monomer selected from the group consisting of acrylamide, methacrylamide, acrylic-, methacrylic-, itaconic-, citraconic-, maleic- and fumaric-acids, N-vinyl pyrrolidone, 2-aminoethylmethacrylate, N-methylaminoethylacrylate, N,N-dimethylaminoethylmethacrylate, acrylonitrile and methacrylonitrile.
Claim 6
Dependent Claim
41 words
The method according to claim 1 wherein monomer (1) is in part replaced by up to about 40% by weight of a monomer selected from the group consisting of alkylacrylates and methacrylates, alkoxyalkylacrylates and methacrylates, styrene, vinyl acetate and maleic anhydride.
Claim 7
Dependent Claim
67 words
The method according to claim 1 wherein group member (3) is selected from the group consisting of benzene, toluene, xylene isomers and mixtures thereof, ethylbenzene, cumene, tetraline, chlorobenzene, 2-chlorotoluene, benzyl chloride, methylene chloride, chloroform, bromoform, tetrachloromethane, ethylene dichloride, trichloroethylene, trichlorotrifluoroethane, ethyl acetate, butyl acetate, isoamyl acetate, di-n-butylphthalate, di-iso-octylphthalate, diethylene glycol dimethyl ether, tri-ethylene glycol dimethyl ether, di-n-butyl ether, di-isopropyl ether, dioxane, tetrahydrofurane, acetone, methylethyl ketone and cyclohexanone.
Claim 8
Dependent Claim
34 words
The method according to claim 1 wherein said group member (3) is admixed with up to about 50% by volume of a member selected from the group consisting of petroleum ether, hexane and cyclohexane.
Claim 9
Dependent Claim
29 words
The method according to claim 1 wherein said polymer product is separated from any excess of said group member (3) by drying at a temperature below about 80° C.
Claim 10
Dependent Claim
22 words
The method according to claim 1 wherein said polymerization is carried out at a temperature of about 20 to about 100° C.
Claim 11
Dependent Claim
34 words
The method according to claim 1 carried out continuously comprising charging monomer (1) with crosslinking agent (2) and group member (3) at a rate sufficient to maintain said concentration of said group member constant.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1981-02-27 | 1981-08-29 | 1982-02-28 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1985-02-27 | 1985-08-29 | 1986-02-28 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1989-02-27 | 1989-08-29 | 1990-02-28 | $7700.00 | Window Closed / Lapsed |