{"title":"CO在过量H2中优于CeO2/CuO催化剂的优先氧化:煅烧温度的影响","authors":"Zhiming Gao , Ming Zhou , Hao Deng , Yong Yue","doi":"10.1016/S1003-9953(11)60399-X","DOIUrl":null,"url":null,"abstract":"<div><p>Different from the classical configuration CuO/CeO<sub>2</sub> catalyst, the inverse configuration CeO<sub>2</sub>/CuO catalyst (atomic ratio of Ce/Cu = 10/100) was prepared by impregnation method. Five calcination temperatures were selected to investigate the interaction between CeO<sub>2</sub> and CuO support. It is found that as calcination temperature increased from 500 to 900°C, sintering of CeO<sub>2</sub> particles on the support occurred together with the diffusion of a portion of Ce<sup>4+</sup> ions into CuO crystals, forming solid solution. Formation of interface complex Ce-O-Cu was suggested by TPR measurements. The catalyst calcined at 700°C gives the highest activity for preferential oxidation of CO in excess H<sub>2</sub> stream.</p></div>","PeriodicalId":56116,"journal":{"name":"Journal of Natural Gas Chemistry","volume":"21 5","pages":"Pages 513-518"},"PeriodicalIF":0.0000,"publicationDate":"2012-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1003-9953(11)60399-X","citationCount":"12","resultStr":"{\"title\":\"Preferential oxidation of CO in excess H2 over CeO2/CuO catalyst: Effect of calcination temperature\",\"authors\":\"Zhiming Gao , Ming Zhou , Hao Deng , Yong Yue\",\"doi\":\"10.1016/S1003-9953(11)60399-X\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Different from the classical configuration CuO/CeO<sub>2</sub> catalyst, the inverse configuration CeO<sub>2</sub>/CuO catalyst (atomic ratio of Ce/Cu = 10/100) was prepared by impregnation method. Five calcination temperatures were selected to investigate the interaction between CeO<sub>2</sub> and CuO support. It is found that as calcination temperature increased from 500 to 900°C, sintering of CeO<sub>2</sub> particles on the support occurred together with the diffusion of a portion of Ce<sup>4+</sup> ions into CuO crystals, forming solid solution. Formation of interface complex Ce-O-Cu was suggested by TPR measurements. The catalyst calcined at 700°C gives the highest activity for preferential oxidation of CO in excess H<sub>2</sub> stream.</p></div>\",\"PeriodicalId\":56116,\"journal\":{\"name\":\"Journal of Natural Gas Chemistry\",\"volume\":\"21 5\",\"pages\":\"Pages 513-518\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1003-9953(11)60399-X\",\"citationCount\":\"12\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Natural Gas Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S100399531160399X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Gas Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S100399531160399X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Preferential oxidation of CO in excess H2 over CeO2/CuO catalyst: Effect of calcination temperature
Different from the classical configuration CuO/CeO2 catalyst, the inverse configuration CeO2/CuO catalyst (atomic ratio of Ce/Cu = 10/100) was prepared by impregnation method. Five calcination temperatures were selected to investigate the interaction between CeO2 and CuO support. It is found that as calcination temperature increased from 500 to 900°C, sintering of CeO2 particles on the support occurred together with the diffusion of a portion of Ce4+ ions into CuO crystals, forming solid solution. Formation of interface complex Ce-O-Cu was suggested by TPR measurements. The catalyst calcined at 700°C gives the highest activity for preferential oxidation of CO in excess H2 stream.