Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67274429 | HCID 67274429 | — |
| Solvent | Water | HCID 962 | — |
| Product | Divinylbenzene-styrene | HCID 174664 | — |
Reaction Steps
This example illustrates the hydrolysis and resuspension of the methylacrylate-divinylbenzene copolymer of Example 7 to produce a weak-acid-functionalized ion exchange resin emulsion. A 200-g sample of the emulsion produced in Example 7 is added to a stirred solution of 57.4 g of 50% aqueous sodium hydroxide solution in 250 ml of water--this represents a 20% excess of base--and the emulsion is observed to coagulate. This mixture is heated to 93° C., held at that temperature for 2 hours, and cooled to room temperature. The coagulum is observed to re-suspend in the sodium hydroxide solution during the stirring and heating period. The emulsion product is diluted to 800-850 ml with water and is passed through a column of Amberlite IR-120 cation exchange resin (trademark of Rohm and Haas Company, Philadelphia, Pa., for a sulfonic acid functionalized, styrene/divinylbenzene gel cation exchange bead resin) in the H+ form to remove the excess sodium hydroxide and convert the product to the free acid form. The solids content of the resulting emulsion is 4.74%, and the weak acid cation exchange capacity is 9.4 meq/g of dry polymer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04359537 |
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| Source dataset | uspto-grants-1982_11 |
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| ORD ID | ord-48b0e42b89d74873b79cdd811f9bc6d7 |
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| Source note | uspto-grants-1982_11 |
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