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dc.contributor.authorDas, J-
dc.contributor.authorLohokare, S P-
dc.contributor.authorChakrabarty, D K-
dc.date.accessioned2019-03-20T06:41:59Z-
dc.date.available2019-03-20T06:41:59Z-
dc.date.issued1992-10-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46240-
dc.description742-746en_US
dc.description.abstractAIPO4-11 as well as substituted SAPO-11 and CoAPO-11 have been synthesized hydrothermally in the pure state. Results of acidity measurement show that the acid strength depends on the substituent. This is also supported by the results of alkylation of toluene with methanol on these catalysts. These molecular sieves exhibit very high para selectively because of the elliptical 10-membered oxygen ring chennals.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.31A(10) [October 1992]en_US
dc.titleSubstituted AIPO4-11 molecular sieves-SAPO-11 and CoAPO-11: Synthesis, acidity and alkylation 'of toluene with methanolen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.31A(10) [October 1992]

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