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制备方法及焙烧温度对Co3O4/CeO2催化剂上CO低温氧化反应的影响
引用本文:邵建军,张平,唐幸福,张保才,宋巍,徐奕德,申文杰.制备方法及焙烧温度对Co3O4/CeO2催化剂上CO低温氧化反应的影响[J].催化学报,2007,28(2):163-169.
作者姓名:邵建军  张平  唐幸福  张保才  宋巍  徐奕德  申文杰
作者单位:1. 装甲兵工程学院装备再制造国防科技重点实验室,北京,100072;中国科学院大连化学物理研究所催化基础国家重点实验室,辽宁大连,116023
2. 装甲兵工程学院装备再制造国防科技重点实验室,北京,100072
3. 中国科学院大连化学物理研究所催化基础国家重点实验室,辽宁大连,116023
摘    要: 分别采用沉淀氧化法、均匀沉淀法及络合燃烧法制备了Co3O4/CeO2复合氧化物催化剂,并在干燥及湿气条件下进行了CO氧化反应. 结果表明,采用沉淀氧化法经538 K焙烧制得的Co3O4/CeO2催化剂具有优异的CO低温氧化活性和较高的抗湿性能. 在196 K条件下,该催化剂上CO氧化的转化率为99%, 并且可连续保持400 min以上; 当温度上升到298 K时,经过 2400 min反应后, CO的转化率仍可达到94%; 当反应气中含3.1%湿气,温度为383 K时,经过2400 min反应后, CO的转化率仍保持在79%. 实验表明, Co3O4/CeO2催化剂的制备方法及焙烧温度对Co3O4与CeO2之间的相互作用有显著的影响,进而影响催化剂催化CO低温氧化的活性.

关 键 词:氧化钴  氧化铈  一氧化碳
文章编号:0253-9837(2007)02-0163-07
收稿时间:2007-02-25
修稿时间:2006-08-22

Effect of Preparation Method and Calcination Temperature on Low-Temperature CO Oxidation over Co3O4/CeO2 Catalyst
SHAO Jianjun,ZHANG Ping,TANG Xingfu,ZHANG Baocai,SONG Wei,XU Yide,SHEN Wenjie.Effect of Preparation Method and Calcination Temperature on Low-Temperature CO Oxidation over Co3O4/CeO2 Catalyst[J].Chinese Journal of Catalysis,2007,28(2):163-169.
Authors:SHAO Jianjun  ZHANG Ping  TANG Xingfu  ZHANG Baocai  SONG Wei  XU Yide  SHEN Wenjie
Institution:1. National Key Laboratory for Remanufacturing, Academy of Armored Force Engineering, Beijing 100072 , China ; 2. State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, The Chinese Academy of Sciences, Dalian 116023, Liaoning, China
Abstract:Co3O4/CeO2 mixed oxides were prepared by coprecipitation-oxidation, homogeneous precipitation, and complexation-combustion methods. The catalysts were used to catalyze low-temperature CO oxidation under dry and humid conditions. The Co3O4/CeO2 catalyst prepared by the coprecipitation-oxidation method followed by calcination at 538 K exhibited excellent activity and good resistance to water vapor poisoning. Remarkably, a CO conversion of 99% was achieved at a temperature as low as 196 K and was maintained more than 400 min under the dry condition. When the reaction was carried out at 298 K, a CO conversion of 94% was obtained after running the reaction for 2 400 min. Even when 3.1% steam was added, a CO conversion of 79% could be kept after 2 400 min time-on-stream at 383 K. It is suggested that the strong interaction between Co3O4 and CeO2 is closely related to the preparation route and the calcination temperature and plays a crucial role in the CO oxidation over the Co3O4/CeO2 catalyst.
Keywords:cobalt oxide  ceria  carbon monoxide
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