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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C2-82
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C9-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C11-04
filingDate 1989-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c09fa7d32f98565be127f32bc8f388dc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31c1b41493a191bc76d92ed4628b0984
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_642f4c7738147156fd0c309374282ee6
publicationDate 1990-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0349419-A1
titleOfInvention Process for preparing a catalyst capable of promoting the oxidative conversion of methane into higher hydrocarbons
abstract First of all, an aqueous phase is brought into contact containing cations of at least one metal from the lanthanide group and cations of at least one alkaline earth metal with a sufficient amount of a source of carbonate ions and optionally a source of hydroxide ions to form a coprecipitate of carbonates and hydroxycarbonates of said metals containing at least 5% by weight of carbonates and bring the pH of the reaction medium to a value greater than 8. The coprecipitate obtained is optionally maintained between 60 ° C and 150 ° C for at least 30 minutes, then it is subjected to washing and then to drying. The washed and dried coprecipitate is finally calcined between 400 ° C and 1000 ° C. The calcined coprecipitate is useful as a catalyst capable of promoting the oxidative conversion of methane to C en hydrocarbons with high activity and selectivity.
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