化学
无机化学
X射线光电子能谱
煅烧
氢氧化物
催化作用
双金属片
混合氧化物
傅里叶变换红外光谱
镍
吸附
氧化物
路易斯酸
碳酸盐
层状双氢氧化物
有机化学
物理
量子力学
核磁共振
作者
Olivier Cairon,Emil Dumitriu,C. Guímon
摘要
The acido-basicity of Mg−Ni−Al mixed oxides generated from the calcination of layered double hydroxides (with the atomic ratios Mg/Ni variable and Mg + Ni/Al equal to 2) has been investigated by adsorption experiments, using FTIR with pyrrole and pyridine as probe molecules and XPS with ammonia and sulfur dioxide. The spectroscopic data were compared with microcalorimetric data and with the results of catalytic tests (cyclohexanol conversion). The acidity, comparable to that of alumina, is mainly of Lewis type. It increases with the nickel content. The FTIR spectra of chemisorbed pyrrole indicate the presence of strong, medium and weak basic sites. The bulk basicity of trimetallic oxides is stronger than that of the bimetallic ones. The effective basicity of the bimetallic Mg−Al oxide is minimized by the presence of numerous remaining carbonate ions. The XPS analyses show that the surface basicity increases with the Mg content, as indicated by the reaction test. Moreover it appears that the majority of the basic surface sites are hydroxyl OH- groups.
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