http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S627732-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1374dd16777534b65ad4422333245af8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G69-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G69-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G69-32
filingDate 1985-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2205edfc410ccf7e6c3230b152bb5bb3
publicationDate 1987-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S627732-A
titleOfInvention Production of wholly aromatic polyamide carrying pendant primary amino group
abstract PURPOSE: To obtain in an industrially stable manner the titled polyamide suitable for, e.g., adhesivity enhancer for aramid fiber, by polymerization between a substituted nitro group-carrying aromatic dicarboxylic acid dichloride and aromatic diamine followed by reduction of the nitro group. n CONSTITUTION: First, a pendant nitro group-carrying wholly aromatic polyamide is prepared by low-temperature polymerization, in the presence of, e.g., an acid acceptor (e.g., alkali metal carbonate) and water, between (A) a 6W22C (constituted by 1W3 aromatic ring) aromatic dicarboxylic acid dichloride carrying 1W2 substituted nitro group per molecule (e.g., 2-nitroterephthaloyl chloride) and (B) an aromatic diamine (e.g., p-phenylenediamine). The objective polyamide can be obtained by reduction, using a reducing agent (e.g., sodium hydrosulfite), in a medium such as water, of said aromatic polyamide. If desired, the component A may be incorporated with 0W50mol% of a nitro group-free analogue thereof. n COPYRIGHT: (C)1987,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012082399-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109337065-A
priorityDate 1985-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 28.