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首页> 外文期刊>International journal of hydrogen energy >Influence of calcination temperature on CuO-CeO2/SiC catalysts for SO3 decomposition in the sulfur-iodine cycle for hydrogen production
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Influence of calcination temperature on CuO-CeO2/SiC catalysts for SO3 decomposition in the sulfur-iodine cycle for hydrogen production

机译:煅烧温度对硫碘循环制氢中SO3分解用CuO-CeO2 / SiC催化剂的影响

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摘要

The copper-cerium composite oxides supported on silicon carbide (SiC) catalysts (CuO-CeO2/SiC) for sulfuric acid decomposition were studied in sulfur-iodine (SI or IS) cycle. The influence of calcination temperatures (800 degrees C-1000 degrees C) of CuO-CeO2/SiC catalysts on their activities and morphology were investigated in this study. The activity of CuO-CeO2/SiC was prominently higher than that of CuO-CeO2 composite oxides catalyst. The SO3 conversion ratio of CuO-CeO2/SiC catalyst increased with calcination temperature from 800 degrees C to 900 degrees C, while decreased with calcination temperature at 900 degrees C-1000 degrees C. XRD pattern, TEM (HRTEM) images and Energy Dispersive X-ray (EDX) spectra revealed that copper-cerium composite oxides were well dispersed and immobilized on the surface of SiC grains. XRD pattern showed that the accelerated transformation of SiC crystals to amorphous SiO2 and the rapid expansion of CeO2 sub-grains at the calcination temperature of 900 degrees C-1000 degrees C, as well as the accelerated amorphization of CuO crystals at 800 degrees C-900 degrees C. The agglomeration of catalysts with sintering temperature was also proven by the BET test. At a higher calcination temperature, X-ray photoelectron spectroscopy (XPS) of Cu-2p spectra revealed the reduction of more Cu2+ in the process of SiC oxidation. According to TEM (HRTEM), XPS, and infrared radiation, the amorphous SiO2 was produced by the oxidation of superficial SiC particles, and the thickness of the SiO2 layers on SiC grains increased with the calcination temperature. A simple mechanism depicted the oxidation of CuO-CeO2/SiC was created. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
机译:以硫碘(SI或IS)循环研究了负载在碳化硅(SiC)催化剂(CuO-CeO2 / SiC)上用于硫酸分解的铜-铈复合氧化物。研究了CuO-CeO2 / SiC催化剂的煅烧温度(800-1000摄氏度)对其活性和形貌的影响。 CuO-CeO2 / SiC的活性明显高于CuO-CeO2复合氧化物催化剂。 CuO-CeO2 / SiC催化剂的SO3转化率随着煅烧温度从800摄氏度增加到900摄氏度而增加,而随着煅烧温度在900摄氏度至1000摄氏度之间而降低。XRD图谱,TEM(HRTEM)图像和能量色散X射线(EDX)光谱表明,铜-铈复合氧化物很好地分散并固定在SiC晶粒的表面上。 XRD图谱表明,在900℃〜1000℃的煅烧温度下,SiC晶体加速转变为非晶态SiO2,CeO2亚晶迅速膨胀,在800℃〜900℃下CuO晶体加速非晶化。 BET试验也证明了催化剂与烧结温度的附聚。在较高的煅烧温度下,Cu-2p光谱的X射线光电子能谱(XPS)显示SiC氧化过程中更多的Cu2 +还原了。根据TEM(HRTEM),XPS和红外辐射,通过表面SiC颗粒的氧化产生了非晶SiO2,并且SiC颗粒上SiO2层的厚度随煅烧温度的增加而增加。创建了描述CuO-CeO2 / SiC氧化的简单机制。 Hydrogen Energy Publications,LLC版权所有(C)2015。由Elsevier Ltd.出版。保留所有权利。

著录项

  • 来源
    《International journal of hydrogen energy》 |2016年第5期|3339-3348|共10页
  • 作者单位

    Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Zhejiang, Peoples R China;

    Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Zhejiang, Peoples R China;

    Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Zhejiang, Peoples R China;

    Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Zhejiang, Peoples R China;

    Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Zhejiang, Peoples R China;

    Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Zhejiang, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Hydrogen production; SO3 decomposition; Cu-Ce/SiC catalyst; Calcination temperature; Oxidation;

    机译:制氢;SO3分解;Cu-Ce / SiC催化剂;煅烧温度;氧化;

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