http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108097327-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_72e6ffa4858f7457fdd0d311a99edb47
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2531-26
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J35-004
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-1691
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-26
filingDate 2016-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7976a3cccf619333bbec7fe030ab8b51
publicationDate 2018-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108097327-A
titleOfInvention The preparation of galapectite modified composite material
abstract The present invention relates to the preparation of galapectite modified composite material, including:It weighs 3.0g galapectites, adds in 75 90mL absolute ethyl alcohols, 3 5g deionized waters after 80 DEG C of 1 3h of reflux, add in 3.0gKH 570, after reaction for 24 hours, washs 3 times with absolute ethyl alcohol, 80 DEG C of dryings, you can obtain the galapectite for being grafted double bond;Weigh 1.25g Zn (NO 3 ) 2 ·6H 2 O, 0.25g amino terephthalic acid (TPA) are dissolved in 33mLDMF, 0.1g, 0.25g and 0.5g carboxylated galapectite, and by transfer reaction kettle after gained suspension ultrasound 20min, 100 DEG C stand 34h.It is collected by centrifugation, 60 80 DEG C of 24 36h of drying, IRMOF 3/COOH HNT composite materials is made.
priorityDate 2016-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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