http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2019514824-A
Outgoing Links
Predicate | Object |
---|---|
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C01B39-04 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J29-85 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C01B39-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C01B37-08 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J29-85 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C01B39-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C01B37-08 |
filingDate | 2017-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2019-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2019514824-A |
titleOfInvention | Method of making SAPO-56, AFX containing molecular sieve |
abstract | The present invention relates to lower alkylamines, preferably trimethylamine, and preferably 1,4- (1,4-diazabicyclo [2.2.2] octane) butyl cation or 1,5-, as a structure directing agent (SDA). Preparation of SAPO-56, (AFX) using 1,4-diazabicyclo [2.2.2] octane derivatives containing any of the (1,4-diazabicyclo [2.2.2] octane) pentyl cations On how to do it. Lower alkyl ammonium hydroxides such as tetrabutyl ammonium hydroxide (TBAOH) can be used to control the pH. The present invention relates to lower alkylamines such as trimethylamine and 1,4-diazabicyclo [2.2.2] octane derivatives such as 1,4- (1,4-diazabicyclo [2.2.2] octane) butyl cation or It also relates to SAPO-56 which comprises a compound comprising any of the 1,5- (1,4-diazabicyclo [2.2.2] octane) pentyl cations. [Selected figure] Figure 1 |
priorityDate | 2016-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 103.