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Please use this identifier to cite or link to this item: http://apo.ansto.gov.au/dspace/handle/10238/5478

Title: Novel CaO-SiO2 Sorbent and Bifunctional Ni/Co-CaO/SiO2 Complex for Selective H-2 Synthesis from Cellulose
Authors: Zhao, M
Yang, X
Church, TL
Harris, AT
Keywords: Hydrogen
Porosity
Catalysis
Gasification
Mixtures
Cellulose
Pyrolysis
Calcium
Oxides
Surface Area
Issue Date: 17-Jan-2012
Publisher: American Chemical Society
Citation: Zhao, M., Yang, X. S., Church, T. L., & Harris, A. T. (2012). Novel CaO-SiO2 Sorbent and Bifunctional Ni/Co-CaO/SiO2 Complex for Selective H-2 Synthesis from Cellulose. Environmental Science & Technology, 46(5), 2976-2983.
Abstract: Catalysis- and sorption-enhanced biomass gasification is a promising route to high-purity hydrogen (H-2); however, most CaO-based sorbents for CO2 capture have poor surface area and mechanical properties, lose carrying capacity over multiple uses, and have insufficient porosity to accommodate extra catalyst sites. We aimed to develop a high-surface-area CaO-SiO2 framework onto which catalysts could be grafted. The best CaO-SiO2 sorbent (n(Ca)/n(Si) = 2:1) maintained a Cao conversion of 65% even after 50 carbonation-decarbonation cycles, better than commercial micrometer-sized CaO or tailored CaO, because of stabilization via Ca-O-Si interactions and an ordered porous structure. Bimetallic catalyst grains (Ni/Co alloy, <20 nm) could be evenly loaded onto this structure by impregnation. The resulting bifunctional complex produced H-2 at nearly the same rate as a mixture of catalyst and commercial CaO while using less total sorbent/catalyst. Furthermore, this complex was much more durable due to its higher coking resistance and stable structure. After 25 carbonation decarbonation cycles, the new catalyst sorbent complex enhanced the H-2 yield from cellulose far more than a mixture of catalyst and commercial CaO did following the same treatment. © 2012, American Chemical Society.
URI: http://dx.doi.org/10.1021/es300135d
http://apo.ansto.gov.au/dspace/handle/10238/5478
ISSN: 0013-936X
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