4.8 Article

Enhanced selective hydrodechlorination of 1,2-dichloroethane to ethylene on Pt-Ag/TiO2 catalysts prepared by sequential photodeposition

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 125, 期 -, 页码 172-179

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcatb.2012.05.016

关键词

Catalytic hydrodechlorination; 1,2-Dichloroethane; Ethylene selectivity; Pt-Ag/TiO2 catalyst; Sequential photodeposition

资金

  1. Natural Science Foundation of China [21107043, 20877039]
  2. Program of New Century Excellent Talents in University [NECT-08-0277]
  3. Natural Science Foundation of Jiangsu Province, China [BK2010378, BK2010051]
  4. Special of Foundation for the Doctor-subject of China [20100091120016]

向作者/读者索取更多资源

TiO2 supported Pt-Ag bimetallic catalysts were prepared using a sequential photodeposition method (denoted as pd-Pt-Ag/TiO2). For comparison, supported bimetallic catalysts were also prepared using the conventional impregnation method (denoted as im-Pt-Ag/TiO2). The catalysts were characterized by X-ray diffraction, transition electron microscopy, CO chemisorption, IR spectroscopy of CO adsorption, and X-ray photoelectron spectroscopy. Characterization results indicated that photodeposition led to site-specific deposition of metallic Ag domain on the surface of Pt particles and thus to the formation of core-shell (Pt@Ag) like bimetallic species, which effectively blocked the adjacent Pt sites. However, Pt-Ag ensemble was predominant in im-Pt-Ag/TiO2. Accordingly, hydrodechlorination of 1,2-dichloroethane exhibited substantially higher ethylene selectivity and catalytic stability on pd-Pt-Ag/TiO2 than on fm-Pt-Ag/TiO2 at similar Ag loading levels. Findings from this study highlight the potential of using sequentially photodeposited core-shell like bimetallic catalysts to enhance the ethylene selectivity in hydrodechlorination of 1,2-dichloroethane. (C) 2012 Elsevier B.V. All rights reserved.

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