{"title":"贵金属催化剂上烃类蒸汽重整(二)","authors":"E. Kikuchi, Y. Yamazaki, Y. Morita","doi":"10.1627/JPI1959.17.3","DOIUrl":null,"url":null,"abstract":"Steam-reforming of n-heptane on rhodium catalysts was investigated under atmospheric pressure and in the temperature range from 550 to 800°C. The degree of dispersion of supported rhodium was determined from hydrogen chemisorption data measured at 25°C by a pulse technique.Rhodium supported on silica was found to sinter considerably on reduction in hydrogen flow, and its activity also decreased. On the other hand, γ-alumina support was found to keep the dispersion of rhodium unchanged on reduction in the temperature range from 550 to 800°C.The activity per weight of a catalyst increased with the concentration of rhodium supported on γ-alumina. The activity was correlated with the amount of hydrogen uptake when more than 0.2% of rhodium was supported.The product composition from reactions at 600°C was compared with the equilibrium composition determined by the following two reactions: i) CH4+H2O=CO+3H2, and ii) CO+H2O=CO2+H2. The composition was found to deviate considerably from the equilibrium at earlier stages of the reaction, but to approach it with increasing conversion of n-heptane. It was suggested that the rate of these equilibrating reactions, especially of the reaction ii), was smaller than that of the initial decomposition of the feed hydrocarbon.","PeriodicalId":9596,"journal":{"name":"Bulletin of The Japan Petroleum Institute","volume":"61 1","pages":"3-8"},"PeriodicalIF":0.0000,"publicationDate":"1975-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":"{\"title\":\"Steam Reforming of Hydrocarbons on Noble Metal Catalysts (Part 2)\",\"authors\":\"E. Kikuchi, Y. Yamazaki, Y. Morita\",\"doi\":\"10.1627/JPI1959.17.3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Steam-reforming of n-heptane on rhodium catalysts was investigated under atmospheric pressure and in the temperature range from 550 to 800°C. The degree of dispersion of supported rhodium was determined from hydrogen chemisorption data measured at 25°C by a pulse technique.Rhodium supported on silica was found to sinter considerably on reduction in hydrogen flow, and its activity also decreased. On the other hand, γ-alumina support was found to keep the dispersion of rhodium unchanged on reduction in the temperature range from 550 to 800°C.The activity per weight of a catalyst increased with the concentration of rhodium supported on γ-alumina. The activity was correlated with the amount of hydrogen uptake when more than 0.2% of rhodium was supported.The product composition from reactions at 600°C was compared with the equilibrium composition determined by the following two reactions: i) CH4+H2O=CO+3H2, and ii) CO+H2O=CO2+H2. The composition was found to deviate considerably from the equilibrium at earlier stages of the reaction, but to approach it with increasing conversion of n-heptane. It was suggested that the rate of these equilibrating reactions, especially of the reaction ii), was smaller than that of the initial decomposition of the feed hydrocarbon.\",\"PeriodicalId\":9596,\"journal\":{\"name\":\"Bulletin of The Japan Petroleum Institute\",\"volume\":\"61 1\",\"pages\":\"3-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1975-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bulletin of The Japan Petroleum Institute\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1627/JPI1959.17.3\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of The Japan Petroleum Institute","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1627/JPI1959.17.3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Steam Reforming of Hydrocarbons on Noble Metal Catalysts (Part 2)
Steam-reforming of n-heptane on rhodium catalysts was investigated under atmospheric pressure and in the temperature range from 550 to 800°C. The degree of dispersion of supported rhodium was determined from hydrogen chemisorption data measured at 25°C by a pulse technique.Rhodium supported on silica was found to sinter considerably on reduction in hydrogen flow, and its activity also decreased. On the other hand, γ-alumina support was found to keep the dispersion of rhodium unchanged on reduction in the temperature range from 550 to 800°C.The activity per weight of a catalyst increased with the concentration of rhodium supported on γ-alumina. The activity was correlated with the amount of hydrogen uptake when more than 0.2% of rhodium was supported.The product composition from reactions at 600°C was compared with the equilibrium composition determined by the following two reactions: i) CH4+H2O=CO+3H2, and ii) CO+H2O=CO2+H2. The composition was found to deviate considerably from the equilibrium at earlier stages of the reaction, but to approach it with increasing conversion of n-heptane. It was suggested that the rate of these equilibrating reactions, especially of the reaction ii), was smaller than that of the initial decomposition of the feed hydrocarbon.