http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2012118-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J20-26
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F8-24
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J20-26
filingDate 1990-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_062a7fdb7a91a1e66aa1e4f29d76f5bc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bb9f5e607700acb19903c7e7295001c
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publicationDate 1990-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2012118-A1
titleOfInvention Process for preparing adsorptive porous resin beads
abstract ABSTRACT Organic materials, for example halocarbons, hydrocarbons or halogenated hydrocarbons are recovered from fluid streams, such as air or water, by passing these streams over post-cross-linked adsorptive porous resin beads. These beads have been prepared by a) haloalkylating cross-linked copolymer beads of i) styrene or an alkylstyrene and ii) divinylbenzene and/or trivinylbenzene, b) purifying the haloalkylated copolymer beads, c) swelling the haloalkylated copolymer beads in an inert organic liquid and post-cross-linking the swollen beads in the presence of a Friedel-Crafts catalyst. The cross-linked copolymer beads which are 36,179-F used in the haloalkylation step are microporous copolymer beads of i) 99.8 to 98.2 weight percent of styrene or an alkylstyrene and ii) 0.2 to 1.8 weight percent of divinylbenzene and/or trivinylbenzene, based on the total weight of i) and ii). 36,179-F
priorityDate 1989-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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