http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105268466-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-141
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-96
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J29-072
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C68-04
filingDate 2014-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ece334956bb0948abdf3a4bbc4e39185
publicationDate 2016-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105268466-A
titleOfInvention Method for preparing Cu-Ni diatom doped mesoporous molecular sieve catalyst
abstract The present invention discloses a method for preparing a Cu-Ni diatom doped mesoporous molecular sieve catalyst. The Cu-Ni diatom doped mesoporous molecular sieve catalyst is prepared by ion thermal synthesis method. First, sodium metaaluminate, silica, water glass, copper sulfate and nickel sulfate are evenly mixed in a high pressure reactor, and then crystallized at 100-140 DEG C for 4h; subsequently, EO20PO70EO20 (P123) is added into the high pressure reactor, an acid functional ionic liquid is used as a template agent for stirring for 20h at constant temperature of 40 DEG C, mesoporous molecular sieve product raw powder is obtained by crystallization, filtration, washing and drying and other processes; finally, the raw powder is calcined in a muffle furnace for 6 hours at 450-550 DEG C to obtain the catalyst. The Cu-Ni diatom doped mesoporous molecular sieve catalyst prepared by the ion thermal synthesis method has high reactivity, good stability and other characteristics in a carbon dioxide ethanol reaction vessel, meanwhile by use of the catalyst, the methanol conversion rate is over 20%, and the DMC selectivity is 95% or more.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114054100-B
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priorityDate 2014-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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