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dc.contributor.authorHe, C.
dc.contributor.authorLi, Qin
dc.contributor.authorLi, P.
dc.contributor.authorWang, Y.
dc.contributor.authorZhang, X.
dc.contributor.authorCheng, J.
dc.contributor.authorHao, Z.
dc.date.accessioned2017-01-30T11:33:53Z
dc.date.available2017-01-30T11:33:53Z
dc.date.created2015-03-03T20:16:47Z
dc.date.issued2010
dc.identifier.citationHe, C. and Li, Q. and Li, P. and Wang, Y. and Zhang, X. and Cheng, J. and Hao, Z. 2010. Templated silica with increased surface area and expanded microporosity: Synthesis, characterization, and catalytic application. Chemical Engineering Journal. 162 (3): pp. 901-909.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/12949
dc.identifier.doi10.1016/j.cej.2010.06.037
dc.description.abstract

In this paper, we report a convenient and effective approach to synthesizing mesoporous SBA-15 materials with increased surface area (up to 836.7 cm3/g) and expanded microporosity (up to 0.22 cm3/g), where the textural properties of the synthesized materials can be systematically controlled. These micro/mesoporous composite materials exhibit excellent performance in catalysis, adsorption and separation. Moreover, the synthesized materials that supported Pd catalysts obtained through impregnation and grafting approaches were tested to explore their flexibility in toluene elimination. Grafting is an effective method to obtain highly dispersed Pd nanoparticles compared with traditional impregnation approach. The catalyst prepared via the grafting procedure possesses higher activity and CO2 selectivity than that was prepared by impregnation method. Moreover, the catalytic performance of synthesized catalysts can be well sustained during the stability tests. Therefore, these novel Pd-supported catalysts are promising materials for effective removal of some types of volatile organic compounds (VOCs) such as toluene.

dc.publisherElsevier BV
dc.titleTemplated silica with increased surface area and expanded microporosity: Synthesis, characterization, and catalytic application
dc.typeJournal Article
dcterms.source.volume162
dcterms.source.startPage901
dcterms.source.endPage909
dcterms.source.issn13858947
dcterms.source.titleChemical Engineering Journal
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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