US4031037A
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Three-dimensional polymeric gel materials containing phosphoric acid residues capable of dissociation and a method for their preparation
Assignee: Individual
•
Filing: 1975-02-20
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Granted: 1977-06-21
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Expires: 1995-02-20
Abstract
Abstract Organic three-dimensional polymeric gel-like materials containing covalently bonded phosphoric acid or a derivative thereof and a method for their manufacture. The bonding is accomplished by the reaction of the free hydroxy or epoxide groups in the homogeneous or macroporous gel-like matrix with the H 3 PO 4 , P 2 O 5 , phosphorus pentahalide and oxyhalide. The halide containing groups may then be hydrolyzed to form acid groups which then may be modified to form complex compounds by reaction with Lewis acids. The gel material may serve as a strongly acidic cation exchanger, catalyst or polymer reagent.
Inventors
- 👤 Jaroslav Kalal
- 👤 Jiri Coupek
- 👤 Svatopluk Pokorny
- 👤 Frantisek Svec
- 👤 Karel Bouchal
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-24 17:18
CPC Classifications
C; C08; C08G; C08G59/00; C08G59/18; C08G59/40; C08G59/4007; C08G59/4071; B; B01; B01J; B01J39/00; B01J39/08; B01J39/12; C08F; C08F8/00; C08F8/40
Claims Analysis
Total Claims: 14
Claim 1
Independent Claim
140 words
An organic polymeric composition prepared by directly reacting a macroporous copolymer matrix of (a) an acrylic or methacrylic acid ester monomer containing at least one functional hydroxyl group or an acrylic or methacrylic acid derivative monomer containing at least one epoxide group and (b) a cross-linking monomer containing at least two double bonds, said cross-linking monomer (b) being at least 10% by weight based on the total weight of the monomers, with a member selected from the group consisting of phosphoric acid, phosphorus pentoxide, phosphorus halide, phosphorus oxyhalide and complexes of phosphoric acid with strong Lewis acids, at a temperature of 0° to 110° C. in the presence of an organic solvent selected from the group consisting of dry benzene, toluene and xylene for at least 2 hours to covalently bond phosphoric acid moieties to said hydroxyl or epoxide groups.
Claim 2
Dependent Claim
140 words
An organic polymeric composition prepared by directly reacting a macroporous copolymer matrix of (a) an acrylic or methacrylic acid ester monomer containing at least one functional hydroxyl group or an acrylic or methacrylic acid derivative monomer containing at least one epoxide group and (b) a cross-linking monomer containing at least two double bonds, said cross-linking monomer (b) being at least 10% by weight based on the total weight of the monomers, with a member selected from the group consisting of phosphoric acid, phosphorus pentoxide, phosphorus halide, phosphorus oxyhalide and complexes of phosphoric acid with strong Lewis acids, at a temperature of 0° to 110° C. in the presence of an organic solvent selected from the group consisting of dry benzene, toluene and xylene for at least 2 hours to covalently bond phosphoric acid moieties to said hydroxyl or epoxide groups.
Claim 3
Dependent Claim
35 words
A composition as defined in claim 1, wherein component (a) is selected from the group consisting of lower alkylene glycol monoacrylates and monomethacrylates, lower polyalkylene glycol monoacrylates and monomethacrylates and lower epoxyalkyl acrylates and methacrylates.
Claim 4
Dependent Claim
46 words
A composition as defined in claim 1, wherein component (a) is selected from the group consisting of hydroxy C 2 to C 6 alkyl acrylates, hydroxy C 2 to C 6 alkyl methacrylates, oligo- or polyglycol acrylates, oligo- or polyglycolmethacrylates and glycidyl acrylate and glycidyl methacrylate.
Claim 5
Dependent Claim
46 words
A composition as defined in claim 1, wherein component (b) is selected from the group consisting of ethylene dimethacrylate, C 2 to C 10 alkylene diacrylates, oligo- or polyglycol diacrylates, oligo- or polyglycol dimethacrylates, di or polyacryloylated or methacryloylated polyfunctional alcohols, triacryloylperhydrotriazine, methylenebismethacrylamide, divinylbenzene and divinylsulfone.
Claim 6
Dependent Claim
66 words
A composition as defined in claim 1, wherein said polymer matrix is a terpolymer matrix additionally containing (c) a monomer selected from the group consisting of styrene, methyl-styrene, C 1 to C 18 alkyl esters of acrylic and methacrylic acids, acrylonitrile, methacrylonitrile, acrylamide, methacrylamide and acryloylmorpholine, said component (c) being present in an amount of 10 to 50% by weight based on the total monomer weight.
Claim 7
Dependent Claim
19 words
A composition as defined in claim 1, wherein the ratio of component (a) to component (b) is about 20:80.
Claim 8
Dependent Claim
153 words
A method of making the organic polymeric composition of claim 1 which comprises directly reacting a macroporous copolymer matrix of an acrylic or methacrylic acid ester monomer containing at least one functional hydroxyl group or an acrylic or methacrylic acid derivative monomer containing at least one epoxide group and (b) a cross-linking monomer containing at least two double bonds wherein said cross-linking monomer is present in an amount of at least 10% based on the total weight of said monomers, with a member selected from the group consisting of phosphoric acid, phosphorus pentoxide, phosphorus halide, phosphorus oxyhalide and complexes of phosphoric acid with strong Lewis acids, at a temperature of 0° to 110° C in the presence of an organic solvent selected from the group consisting of dry benzene, toluene and xylene for at least 2 hours to covalently bond phosphoric acid moieties to said hydroxyl or epoxide groups and recovering said copolymer.
Claim 9
Dependent Claim
202 words
A method of making the organic polymeric composition of claim 5, which comprises directly reacting a macroporous terpolymer matrix of (a) an acrylic or methacrylic acid ester monomer containing at least one functional hydroxyl group or an acrylic or methacrylic acid derivative monomer containing at least one epoxide group and (b) a cross-linking monomer containing at least two double bonds and (c) a monomer selected from the group consisting of styrene, methylstyrene, C 1 to C 18 alkyl esters of acrylic and methacrylic acids, acrylonitrile, methacrylonitrile, acrylamide, methacrylamide and acryloylmorpholine, said cross-linking monomer being present in an amount of at least 10% by weight based on the total weight of said monomers and said component (c) being present in an amount of 10 to 50% by weight based on the total monomer weight, with a member selected from the group consisting of phosphoric acid, phosphorus pentoxide, phosphorus halide, phosphorus oxyhalide and complexes of phosphoric acid with strong Lewis acids at a temperature of 0° to 110° C in the presence of an organic solvent selected from dry benzene, toluene and xylene for at least 2 hours to covalently bond phosphoric acid moieties to said hydroxyl or epoxide groups, and recovering said terpolymer.
Claim 10
Dependent Claim
25 words
Method according to claim 7, wherein said organic solvent is a solvent for the copolymer of (a) and (b) but not for the phorphorylated copolymer.
Claim 11
Dependent Claim
26 words
Method according to claim 7, wherein about 1 mol of phosphorylating agent is employed for each mol equivalent of hydroxyl or epoxide groups in said copolymer.
Claim 12
Dependent Claim
10 words
A catalyst consisting essentially of the composition of claim 1.
Claim 13
Dependent Claim
16 words
A coordination complex consisting essentially of the composition of claim 1 complexed with a Lewis acid.
Claim 14
Dependent Claim
12 words
A cation exchange composition consisting essentially of the composition of claim 1.
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) | 1980-06-20 | 1980-12-20 | 1981-06-21 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1984-06-20 | 1984-12-20 | 1985-06-21 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1988-06-20 | 1988-12-20 | 1989-06-21 | $7700.00 | Window Closed / Lapsed |