{"title":"Reduction of NO by CO over alumina-supported palladium catalyst","authors":"H. Muraki, H. Shinjoh, Y. Fujitani","doi":"10.1021/I300023A009","DOIUrl":null,"url":null,"abstract":"The kinetics of NO reduction by CO have been investigated over a Pd/Al/sub 2/O/sub 3/ catalyst. These studies have been complemented by pulse reaction, transient response method, and TPD. The performance of the Pd catalyst depended strongly on the ratio of NO/CO and the reaction temperature. It was shown that the N/sub 2/O selectivity was minimum at the stoichiometric ratio of NO/CO. For NO conversion below 20% at 350/sup 0/C, the kinetics for NO reduction and N/sub 2/ and N/sub 2/O formation over Pd catalysts were first order in NO and inverse first order in CO. The kinetics and product selectivity were found to be in good agreement with a mechanism based on the chemisorption of NO as the rate-limiting step.","PeriodicalId":13540,"journal":{"name":"Industrial & Engineering Chemistry Product Research and Development","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1986-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Industrial & Engineering Chemistry Product Research and Development","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/I300023A009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 19
Abstract
The kinetics of NO reduction by CO have been investigated over a Pd/Al/sub 2/O/sub 3/ catalyst. These studies have been complemented by pulse reaction, transient response method, and TPD. The performance of the Pd catalyst depended strongly on the ratio of NO/CO and the reaction temperature. It was shown that the N/sub 2/O selectivity was minimum at the stoichiometric ratio of NO/CO. For NO conversion below 20% at 350/sup 0/C, the kinetics for NO reduction and N/sub 2/ and N/sub 2/O formation over Pd catalysts were first order in NO and inverse first order in CO. The kinetics and product selectivity were found to be in good agreement with a mechanism based on the chemisorption of NO as the rate-limiting step.
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