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dc.creatorRajić, Nevenka
dc.creatorStojaković, Djordje
dc.creatorKaučič, Venčeslav
dc.date.accessioned2022-04-15T13:12:51Z
dc.date.available2022-04-15T13:12:51Z
dc.date.issued1991
dc.identifier.issn0004-9425
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/5056
dc.description.abstractThe SAPO, MeAPO and MeSAPO microporous materials (Me=Co2+ and/or 2n2+) having a sodalite structure have been obtained hydrothermally at 200°C in the presence of tetramethylammonium ion as the template. The SAPO and MeSAPO products prepared at lower template concentrations are formed through a partial replacement of both aluminium and phosphorus by silicon in the parent aluminophosphate lattice; at higher pH only phosphorus is replaced. While the Me2+ ions are in all cases constituents of the framework, most zinc-containing materials have a fraction of the Zn2+ ions located in the cavities. T.g.a . shows that complete removal of the trapped organic component can not be easily accomplished. This can be explained by the small size of the openings in the sodalite cages. Powder diffraction analysis shows that replacement of aluminium by silicon, cobalt and zinc, and phosphorus by silicon leads to an expansion of the parent aluminophosphate unit cell. Kinetic studies suggest that crystallization of the silicon-containing products is preceded by an induction period of about 2 h, the nucleation taking place both in the liquid and solid phase.sr
dc.language.isoensr
dc.publisherCSIRO PUBLISHINGsr
dc.rightsrestrictedAccesssr
dc.sourceAustralian Journal of Chemistrysr
dc.titlePreparation and Properties of Sodalite-Type Aluminophosphates Containing Silicon, Cobalt and Zincsr
dc.typearticlesr
dc.rights.licenseARRsr
dc.citation.epage553
dc.citation.issue4
dc.citation.spage543
dc.citation.volume44
dc.identifier.doi10.1071/CH9910543
dc.identifier.scopus2-s2.0-84970551366
dc.type.versionpublishedVersionsr


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