http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105668585-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C01P2004-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C01P2004-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C01P2004-03
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C01B39-32
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C01B39-32
filingDate 2016-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2018-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105668585-B
titleOfInvention Method for preparing L-type zeolite using directing agent
abstract The invention relates to a method for preparing L-type zeolite directing agent and using the directing agent to prepare the L-type zeolite. The preparation method of the L-type zeolite is as follows: the molar ratio formula range is as follows: K 2 O/(K 2 O+Na 2 O)=0.6-1:1, (K 2 O+Na 2 O)/SiO 2 =0.35-0.5:1, SiO 2 /Al 2 O 3 =1:0.003-0.0005, solvent/(K 2 O+Na 2 ( O)=100-1000:1, template R/SiO 2 =0.01-0.02:1 synthetic mixture, add the directing agent, stir evenly, add the corresponding template R, microwave heating to 150°C to crystallize, react After 24 hours, the colloidal suspension of the L-type zeolite was obtained, and the colloidal suspension was centrifuged with a high-speed centrifuge. After removing the supernatant, the remaining precipitate was repeatedly washed with water, and then washed with absolute ethanol. Clean until the clear liquid is colorless. After drying, the L-type zeolite is obtained. The molar ratio of the solid components in the formula is calculated according to the oxide.
priorityDate 2016-01-04-04:00^^<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: 42.