http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101415483-B1

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-265
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C63-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-47
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-265
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C63-26
filingDate 2007-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2014-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101415483-B1
titleOfInvention Method for producing isophthalic acid
abstract Isophthalic acid is subjected to solid-liquid separation to obtain a mother liquor. (1) The mother liquor is adjusted to a bromine ratio of 0.3 to 3 and then brought into contact with a pyridine ring-containing chelating resin heated at 35 to 140 ° C to form a heavy metal ion (2) contacting the pyridine ring-containing chelating resin having undergone the adsorption step with a water acetic acid having a water concentration of 1 to 15% by weight to form a mixture containing the by-produced carboxylic acid mixture An eluting step (A) for obtaining an eluent, (3) an eluting step (B) for obtaining an eluent containing heavy metal ions and bromide ions derived from the catalyst, and (4) a series of replacement steps for regenerating the pyridine ring- Wherein the catalyst is recovered and at least a part of the catalyst is reused for the liquid phase oxidation reaction.
priorityDate 2006-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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