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Enhanced catalytic performance for CO oxidation and preferential CO oxidation over CuO/CeO_2 catalysts synthesized from metal organic framework: Effects of preparation methods

机译:与金属有机骨架合成的CuO / CeO_2催化剂相比,增强了CO氧化的催化性能和优先CO氧化:制备方法的影响

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In this paper, CuO/CeO2 catalysts derived from Ce-BTC metal organic framework as the precursor were synthesized by various methods (in-situ synthesis method, mechanical mixing method and impregnation method). The precursors and catalysts were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), N-2 adsorption-desorption, H-2-temperature program reduction (H-2-TPR), inductively coupled plasma optical emission spectroscopy (ICP-OES) and X-ray photoelectron spectroscopy (XPS). It was found that the preparation methods strongly affected the low temperature reduction behavior and oxygen vacancies of CuO/CeO2 catalysts. The CuCeO-ETH catalyst showed excellent catalytic activity for CO oxidation (T-100 = 100 degrees C). Meanwhile, a broad temperature window to match CO conversion and selectivity higher than 98% at the same time appeared for preferential CO oxidation. In addition, the CuCeO-ETH catalyst displayed high reaction stability and CO catalytic performance for CO oxidation and preferential CO oxidation even after three cycles. The addition of H2O and CO2 in the stream caused a lightly decrease in the CO conversion. The CuCeO-ETH catalyst still maintains a CO conversion of 100% at 130 degrees C. The improved catalytic performance for CO oxidation and preference CO oxidation could be attributed to easily reducible surface copper species, more Cu+ oxygen vacancies and surface lattice oxygen. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:本文采用多种方法(原位合成法,机械混合法和浸渍法)合成了以Ce-BTC金属有机骨架为前驱体的CuO / CeO2催化剂。通过扫描电子显微镜(SEM),X射线衍射(XRD),N-2吸附-解吸,H-2温度程序还原(H-2-TPR),电感耦合等离子体发射光谱法对前体和催化剂进行了表征(ICP-OES)和X射线光电子能谱(XPS)。发现该制备方法强烈影响CuO / CeO2催化剂的低温还原行为和氧空位。 CuCeO-ETH催化剂显示出出色的CO氧化催化活性(T-100 = 100摄氏度)。同时,出现了宽广的温度窗口以匹配CO转化率,同时选择性高于98%,可以优先进行CO氧化。另外,即使在三个循环之后,CuCeO-ETH催化剂也显示出高的反应稳定性和对CO氧化和优先CO氧化的CO催化性能。物流中加入H2O和CO2导致CO转化率略有下降。 CuCeO-ETH催化剂在130摄氏度下仍保持100%的CO转化率。改进的CO氧化和优先CO氧化性能可归因于易于还原的表面铜物种,更多的Cu +氧空位和表面晶格氧。 (C)2018氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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