http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1051589-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G64-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G64-24
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G64-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G63-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G64-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G64-24
filingDate 1975-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1979-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_60082d9876ab1a5cae99f18c30f3661c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_890b038ceb5e9d16d67bfced2783e0e4
publicationDate 1979-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1051589-A
titleOfInvention Phase boundary process for the preparation of aromatic polycarbonates using a chlorinated aromatic hydrocarbon as the polymer solvent
abstract A PHASE BOUNDARY PROCESS FOR THE PREPARATION OF AROMATIC POLYCARBONATES USING A CHLORINATED AROMATIC HYDROCARBON AS THE POLYMER SOLVENT Abstract of the Invention The present invention provides a process for the preparation of a polycarbonate by the phase boundary conden-sation method, by phosgenation of an aqueous alkali metal salt solution of one or more aromatic dihydroxy compounds, in which process an aromatic chlorinated hydrocarbon is used as the solvent and the synthesis of the polycarbonate is carried out in two stages, in the first stage of which the reaction of the alkali metal salt solution of the aromatic dihydroxy compound(s) with phosgene is carried out at an OH concentration of between 0.01 and 0.1% by weight of OH, relative to the aqueous phase, in the presence of 0.1 to 2.5 mol% of trialkyl-amine, relative to aromatic dihydroxy compound(s), and at a temperature higher than 70°C, with a dwell time of less than 5 minutes, while in the second stage the polycondensation is effected by adjusting the OH concentration to 0.20 to 0.50% by weight of OH, relative to the aqueous phase, optionally with further addition of trialkylamine, at a temperature higher than 80°C and with a dwell time of more than 1 minute. .
priorityDate 1974-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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