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首页> 外文期刊>Applied Surface Science >Selective hydrodechlorination of 1,2-dichloroethane catalyzed by trace Pd decorated Ag/Al2O3 catalysts prepared by galvanic replacement
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Selective hydrodechlorination of 1,2-dichloroethane catalyzed by trace Pd decorated Ag/Al2O3 catalysts prepared by galvanic replacement

机译:电流置换制备的痕量钯装饰Ag / Al2O3催化剂选择性催化1,2-二氯乙烷加氢脱氯。

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摘要

Ag catalysts decorated by trace Pd supported on gamma-Al2O3 with different structure and chemical properties were prepared using a combined impregnation and galvanic replacement method. For comparison, monometallic Ag/gamma-Al2O3 and Pd/gamma-Al2O3 catalysts were prepared using the impregnation method. Gas-phase catalytic hydrodechlorination of 1,2-dichloroethane to ethylene was investigated on those catalysts. The structures and chemical compositions of bimetallic Pd-Ag particles in the catalysts were controlled by adjusting Pd replacement amount. The as-prepared catalysts were characterized by X-ray diffraction, transmission electron microscopy, UV-vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, and in-situ FTIR spectroscopy of CO adsorption. The results demonstrated that contiguous Pd sites dominated in the monometallic Pd/gamma-Al2O3 catalyst, while Pd atoms were separately decorated on the surface of Ag particles in the bimetallic Pd/gamma-Al2O3 catalysts when Pd replacement amount was below 0.30 wt.%. At Pd replacement amount of 0.30 wt.%, Pd ensembles with contiguous Pd sites developed in the bimetallic catalyst. Thus, monometallic Pd/gamma-Al2O3 catalyst displayed negligible ethylene selectivity toward the catalytic hydrodechlorination of 1,2-dichloroethane, while bimetallic Pd/gamma-Al2O3 catalyst with a Pd replacement amount of 0.13 wt.% exhibited 94.6% of ethylene selectivity. Furthermore, selectivity to incompletely dechlorinated byproduct chloroethylene decreased with Pd replacement amount, due to the enhanced decoration effect of Pd on large Ag ensembles. Findings in this work provide a promising bimetallic catalyst prepared by galvanic replacement for the selective catalytic hydrodechlorination of 1,2-dichloroethane. (C) 2017 Elsevier B.V. All rights reserved.
机译:采用浸渍和电置换相结合的方法,制备了负载在γ-Al2O3上的痕量Pd修饰的Ag催化剂。为了比较,使用浸渍法制备了单金属Ag /γ-Al2O3和Pd /γ-Al2O3催化剂。在这些催化剂上研究了1,2-二氯乙烷的气相催化加氢脱氯制乙烯。通过调节Pd的置换量来控制催化剂中双金属Pd-Ag颗粒的结构和化学组成。通过X射线衍射,透射电子显微镜,UV-vis漫反射光谱,X射线光电子光谱和CO吸附原位FTIR光谱对所制备的催化剂进行表征。结果表明,当Pd置换量低于0.30wt。%时,在单金属Pd /γ-Al2O3催化剂中,连续的Pd位点占主导,而在双金属Pd /γ-Al2O3催化剂中,Ag颗粒表面上分别装饰有Pd原子。在Pd替换量为0.30重量%时,Pd与在双金属催化剂中形成的连续的Pd位点聚集。因此,单金属Pd /γ-Al2 O 3催化剂对1,2-二氯乙烷的催化加氢脱氯显示出可忽略的乙烯选择性,而Pd替代量为0.13重量%的双金属Pd /γ-Al2 O 3催化剂显示出94.6%的乙烯选择性。此外,由于Pd对大型Ag团簇的装饰效果增强,对不完全脱氯的副产物氯乙烯的选择性随Pd置换量而降低。在这项工作中的发现提供了一种有前途的双金属催化剂,该双金属催化剂是通过电流置换制备的,用于1,2-二氯乙烷的选择性催化加氢脱氯。 (C)2017 Elsevier B.V.保留所有权利。

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  • 来源
    《Applied Surface Science 》 |2018年第15期| 703-709| 共7页
  • 作者单位

    Nanjing Univ, Sch Environm, Jiangsu Key Lab Vehicle Emiss Control, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Jiangsu, Peoples R China;

    Nanjing Univ, Sch Environm, Jiangsu Key Lab Vehicle Emiss Control, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Jiangsu, Peoples R China;

    Nanjing Univ, Sch Environm, Jiangsu Key Lab Vehicle Emiss Control, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Jiangsu, Peoples R China;

    Nanjing Univ, Sch Environm, Jiangsu Key Lab Vehicle Emiss Control, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Jiangsu, Peoples R China;

    Nanjing Univ, Sch Environm, Jiangsu Key Lab Vehicle Emiss Control, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Jiangsu, Peoples R China;

    Nanjing Univ, Sch Environm, Jiangsu Key Lab Vehicle Emiss Control, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Jiangsu, Peoples R China;

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  • 正文语种 eng
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  • 关键词

    1,2-Dichloroethane; Catalytic hydrodechlorination; Pd decoration; Ethylene selectivity; Galvanic replacement;

    机译:1,2-二氯乙烷;催化加氢脱氯;钯装饰;乙烯选择性;电取代;

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