Claims
- 1. 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 .alpha.-.beta.-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.
- 2. Cation exchange resin beads of claim 1 wherein the apparent density of the resin beads is not greater than 1.0 g/ml.
- 3. 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.
- 4. 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 .alpha.-.beta.-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.
- 5. The process of claim 4 wherein said organic liquid is selected from the group consisting of an aliphatic hydrocarbon and an aliphatic alcohol.
- 6. 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.
- 7. 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.
- 8. The process of claim 4 wherein said monoethylenically unsaturated monomer is styrene and said polyethylenically unsaturated monomer is divinylbenzene.
Parent Case Info
This is a division of application Ser. No. 749,526 filed July 12, 1958, now U.S. Pat. No. Des. 250,972.
US Referenced Citations (11)
Non-Patent Literature Citations (2)
Entry |
Abrams-Industrial Engineering Chemistry, vol. 48, pp. 1469-1472 (1956). |
Schildknecht-Polymer Processes, pp. 82-83, (1956), Interscience. |
Divisions (1)
|
Number |
Date |
Country |
Parent |
749526 |
Jul 1958 |
|