维普中文期刊产品整合服务

Rare earth oxides doped NiO/γ-Al_2O_3 catalyst for oxidative dehydrogenation of cyclohexane

查看全文 作  者:Hany M.AbdelD [1,2,3]ayem;[4]M.Faiz;Hesham S.Abdel-[3,5]Samad;Salah [3]A.Hassan 高影响力作者 机构地区:[1]Center of Research Excellence in Petroleum Refining & Petrochemicals (CoR E-PRP), King Fahd University of Petroleum & Minerals;[2]Chemistry Department, College of Science, King Faisal University;[3]Chemistry Department,Faculty of Science, Ain Shams University;[4]Surface Science Laboratory, Physics Department, King Fahd University of Petroleum &Minerals;[5]Department of Basic Sciences and Technology, Community College, Taibah University高影响力机构 出  处:《Journal of Rare Earths》索引2015年第33卷第6期,共8页高影响力期刊 基  金:the Center of Research Excellence in Petroleum Refining & Petrochemicals (project: CoRE-PRP-06) established by the Ministry of Higher Education at the King Fahd University of Petroleum & Minerals, Dhahran, Saudi Arabia for finical support of this work 摘  要:The effect of rare earth oxides(RE=Ce, La, Gd, and Dy) doping of alumina support in NiO/γ-Al2O3 system was investigated on its catalytic performance in oxidative dehydrogenation(ODH) of cyclohexane. The physicochemical properties of various samples were followed up through N2 physisorption, temperature programmed reduction(H2-TPR), X-ray diffraction(XRD), X-ray photoelectron spectroscopy(XPS) and potentiometric acid-base titration techniques. In the parent NiO/γ-Al2O3 catalyst, Ni species were found to be strongly interacted with alumina surface. Addition of rare earth dopants to γ-Al2O3 in the catalyst system affected the nickel-alumina interaction and resulted in significant modifications in the catalytic performances in the ODH reaction. The results revealed the beneficial role of both La2O3 and Gd2O3 doping in enhancing the ODH catalytic activity and selectivity to cyclohexene. H2-TPR and XPS results indicated that majority of Ni species in NiO/La2O3 modified γ-Al2O3 were more weakly interacted with La2O3 and alumina whereas both NiO like species and nickel aluminate were present on the surface. Doping with cerium or dysprosium increased the nickel-support interaction and led to a decrease in surface nickel concentration. In case of doping with Ce, surface concentration of cerium oxide was higher than those of the other RE oxides; the doped catalyst reached its steady state activity faster than the other catalysts. The acid-base results suggested that RE metals were interacted most likely with acidic surface hydroxyl groups. The degree of nickel-alumina interaction decreased in the following order: LaAl>GdAl>CeAl>DyAl. 关 键 词:催化剂体系 氧化物掺杂 稀土氧化物 氧化脱氢 NIO 环己烷 X-射线光电子能谱 氧化铝载体
相关文献

参考文献(38)

引证文献(7)

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费