Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/45749
標題: Effects of acid treatments of activated carbon on its physiochemical structure as a support for copper oxide in DeSO(2) reaction catalysts
作者: Tseng, H.H.
魏銘彥
Wey, M.Y.
關鍵字: activated carbon;surface oxygen groups;Cu/AC catalyst;acid treatment;adsorption properties;flue-gas desulfurization;sulfur-dioxide;surface-chemistry;ammonia-synthesis;so2 oxidation;no reduction;nitric-acid;adsorption;sorbent;regeneration
Project: Chemosphere
期刊/報告no:: Chemosphere, Volume 62, Issue 5, Page(s) 756-766.
摘要: 
To enhance the dispersion of active sites, modification of the AC supports with different acid solution might result in various surface oxygen groups which act as anchoring sites for metallic precursor to stay and improve the reactivity between AC supports and copper precursor. In the present work, the AC support is tailored with HCl and HNO3, respectively. The pore structure, surface oxygen groups of the AC support and catalysts as well as catalyst dispersion before and after acid treatments are systematically studied by BET, pH(slurry), TPD, and XRPD analyses. It is found that the order of activity in DeSO(2) reaction is as follows: Cu/AC-HCI > Cu/AC > Cu/AC-HNO3. The same sequence is also observed for the pore structure of AC supports, the catalyst dispersion, but not for the amounts of CO2 evolving during TPD experiments of supports. The key role of acid treatment on carbon surface chemistry and pore structure, which are closly related to catalyst dispersion and adsorption capacity, is examined to rationalize these findings. Furthermore, under the NO/NH3 = 1 the NO could be selective catalytic reduction with NH3 in the presence of O-2, which catalyzed by fresh and spent AC-supported catalyst. (c) 2005 Elsevier Ltd. All rights reserved.
URI: http://hdl.handle.net/11455/45749
ISSN: 0045-6535
DOI: 10.1016/j.chemosphere.2005.04.077
Appears in Collections:環境工程學系所

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