Patent US3612164A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4256840A Expired / Lapsed US ⏱️ 0.0 years remaining

Macroreticular cation exchange beads and preparation of same

Assignee: Rohm and Haas Co
•
Filing: 1979-05-21
•
Granted: 1981-03-17
•
Expires: 1999-05-21
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract Process for preparing cation exchange resin having macroreticular structure, high surface area and lowered apparent density from a macroreticulated copolymer produced by copolymerizing a mixture of a monoethylenically unsaturated monomer and a polyethylenically unsaturated monomer dissolved in an organic liquid which is a solvent for said monomers but unable to substantially swell the resulting copolymer, and macroreticulated cation exchange resin beads produced by the process.

Inventors

  • 👤 Erich F. Meitzner
  • 👤 James A. Oline

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 17:48
CPC Classifications
C; C08; C08F; C08F2/00; C08F2/12; C08F2/16; C08F2/18; B; B01; B01D; B01D15/00; B01D15/08; B01D15/26; B01D15/36; B01D15/361; B01J; B01J20/00; B01J20/22; B01J20/26; B01J39/00; B01J39/08; B01J39/16; B01J39/18; B01J39/20; B01J41/00; B01J41/08; B01J41/12; B01J41/14; C08F2/14; C08F36/00; C08F36/02; C08F36/20; C08F8/00; C08F8/30; C08F8/32; C08F8/44; C08J; C08J9/00; C08J9/28; C08J9/286; C08J2357/00

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 194 words
Cation exchange resin beads of macroreticular structure, high surface area, and lowered apparent density crosslinking essentially of a macroreticular crosslinked copolymer matrix with cation exchange functional groups bonded thereto, said resin beads having (1) an apparent density of at least 0.02 density units less than, and (2) a surface area much greater than gel-type ion exchange beads of the same composition, said beads resulting from the presence therein of microscopic channels or voids of much larger dimensions than the micropores of gel-type ion exchange beads of the same composition, and which crosslinked copolymer matrix is prepared by copolymerizing a mixture consisting essentially of (i) a monovinyl carbocyclic aromatic compound or an ester of an acrylic or methacrylic acid, with (ii) a polyethylenically unsaturated monomer selected from the group consisting of a polyvinyl carbocyclic aromatic compound, an ester of a dihydric alcohol and an α-β-ethylenically unsaturated carboxylic acid, diallyl maleate, and divinyl ketone, the copolymerization being conducted while the monomers are dissolved in a phase separating amount of an organic liquid or mixture of organic liquids which is a solvent for said monomers but which is unable to substantially swell the copolymers resulting from copolymerization.
Claim 2
Dependent Claim 194 words
Cation exchange resin beads of macroreticular structure, high surface area, and lowered apparent density crosslinking essentially of a macroreticular crosslinked copolymer matrix with cation exchange functional groups bonded thereto, said resin beads having (1) an apparent density of at least 0.02 density units less than, and (2) a surface area much greater than gel-type ion exchange beads of the same composition, said beads resulting from the presence therein of microscopic channels or voids of much larger dimensions than the micropores of gel-type ion exchange beads of the same composition, and which crosslinked copolymer matrix is prepared by copolymerizing a mixture consisting essentially of (i) a monovinyl carbocyclic aromatic compound or an ester of an acrylic or methacrylic acid, with (ii) a polyethylenically unsaturated monomer selected from the group consisting of a polyvinyl carbocyclic aromatic compound, an ester of a dihydric alcohol and an α-β-ethylenically unsaturated carboxylic acid, diallyl maleate, and divinyl ketone, the copolymerization being conducted while the monomers are dissolved in a phase separating amount of an organic liquid or mixture of organic liquids which is a solvent for said monomers but which is unable to substantially swell the copolymers resulting from copolymerization.
Claim 3
Dependent Claim 21 words
Cation exchange resin beads of claim 1 wherein the apparent density of the resin beads is not greater than 1.0 g/ml.
Claim 4
Dependent Claim 24 words
Cation exchange resin beads of claim 1 wherein the microscopic channels or voids comprise at least about 17.5% by volume of the resin beads.
Claim 5
Dependent Claim 150 words
In a process for preparing a cation exchange resin having a water insoluble matrix and cation exchange groups bonded thereto, the improvement comprising employing as said matrix a solid copolymer of macroreticular structure which is permeated by small channels or voids into which liquids are able to penetrate, which matrix is prepared by copolymerizing a mixture consisting essentially of (1) a monovinyl carbocyclic aromatic compound or an ester of an acrylic or methacrylic acid, with (2) a polyethylenically unsaturated monomer selected from the group consisting of a polyvinyl carbocyclic aromatic compound, an ester of a dihydric alcohol and an α-β-ethylenically unsaturated carboxylic acid, diallyl maleate, and divinyl ketone, the copolymerization being conducted while the monomers are dissolved in a phase separating amount of an organic liquid or mixture of organic liquids which is a solvent for said monomers but which is unable to substantially swell the copolymers resulting from copolymerization.
Claim 6
Dependent Claim 150 words
In a process for preparing a cation exchange resin having a water insoluble matrix and cation exchange groups bonded thereto, the improvement comprising employing as said matrix a solid copolymer of macroreticular structure which is permeated by small channels or voids into which liquids are able to penetrate, which matrix is prepared by copolymerizing a mixture consisting essentially of (1) a monovinyl carbocyclic aromatic compound or an ester of an acrylic or methacrylic acid, with (2) a polyethylenically unsaturated monomer selected from the group consisting of a polyvinyl carbocyclic aromatic compound, an ester of a dihydric alcohol and an α-β-ethylenically unsaturated carboxylic acid, diallyl maleate, and divinyl ketone, the copolymerization being conducted while the monomers are dissolved in a phase separating amount of an organic liquid or mixture of organic liquids which is a solvent for said monomers but which is unable to substantially swell the copolymers resulting from copolymerization.
Claim 7
Dependent Claim 23 words
The process of claim 4 wherein said organic liquid is selected from the group consisting of an aliphatic hydrocarbon and an aliphatic alcohol.
Claim 8
Dependent Claim 39 words
The process of claim 4 wherein said monomers dissolved in said organic liquid are suspended in an aqueous medium and polymerization is effected in said suspension to obtain the copolymer in the form of resin beads of macroreticular structure.
Claim 9
Dependent Claim 35 words
The process of claim 4 wherein said cation exchange groups are sulfonic acid groups, said monoethylenically unsaturated monomer is a monovinyl carbocyclic aromatic compound, and said polyethylenically unsaturated monomer is a polyvinyl carbocyclic aromatic compound.
Claim 10
Dependent Claim 19 words
The process of claim 4 wherein said monoethylenically unsaturated monomer is styrene and said polyethylenically unsaturated monomer is divinylbenzene.

References Cited (Backward Citations)

US2366008A Cited
US2500149A Cited
US2591573A Cited
US2591574A Cited
US2540984A Cited
US2643995A Cited
US2629710A Cited
US2597440A Cited
US2862892A Cited
US3586646A Cited
US3549562A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-03-16 1984-09-15 1985-03-17 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-03-16 1988-09-15 1989-03-17 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-03-16 1992-09-15 1993-03-17 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag