首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Bismuth supported SBA-15 catalyst for vapour phase Beckmann rearrangement reaction of cyclohexanone oxime to epsilon-caprolactam
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Bismuth supported SBA-15 catalyst for vapour phase Beckmann rearrangement reaction of cyclohexanone oxime to epsilon-caprolactam

机译:铋负载的SBA-15催化剂,用于环己酮肟与ε-己内酰胺的气相贝克曼重排反应

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Development of environmental benign as well as low cost metal precursor based catalyst is a challenge for chemical industry. In this work we report Bi promoted SBA-15 catalyst for vapour phase Beckmann rearrangement reaction of cyclohexanone oxime. The three different Bi loaded SBA-15 catalysts are prepared and characterized by BET surface area and porosity measurement, small angle X-ray scattering, wide angle X-ray diffraction, field emission scanning electron microscope, high resolution transmission electron microscope, ultraviolet-visible spectroscope, Fourier transform infrared spectroscopy and temperature programmed desorption techniques. Further, catalytic activity is optimized by changing reaction temperature, pre-treatment temperature and pre-treatment time so that 100% cyclohexanone oxime conversion and 100% epsilon-caprolactam selectivity has been achieved. Role of solvent, silylation and time on stream has also been examined. The TPD profiles of all three bismuth loaded samples are mainly characterized by weak acidic sites or surface silanol groups. The FTIR profile shows hydroxyl rich surface in the vicinity of bismuth at Bi-SBA-15 (Bi/Si = 1/100). Based on catalyst characterization and activity data correlation, it can be suggested that protonation at oxime oxygen can be triggered by surface silanol in the vicinity of a Lewis acid centre bismuth. The high space-time-yield of caprolactum was 114.3 mol g(cat)(-1) h(-1) was obtained. (C) 2015 Elsevier B.V. All rights reserved.
机译:开发环境友好的以及低成本的基于金属前体的催化剂是化学工业的挑战。在这项工作中,我们报道了Bi促进SBA-15催化剂用于环己酮肟的气相贝克曼重排反应。制备了三种不同的Bi负载SBA-15催化剂,并通过BET表面积和孔隙率测量,小角X射线散射,广角X射线衍射,场发射扫描电子显微镜,高分辨率透射电子显微镜,紫外可见光进行了表征。光谱仪,傅立叶变换红外光谱仪和程序升温解吸技术。此外,通过改变反应温度,预处理温度和预处理时间来优化催化活性,从而实现了100%的环己酮肟转化率和100%的ε-己内酰胺选择性。还检查了溶剂,甲硅烷基化和生产时间的作用。所有三个铋负载样品的TPD谱图的主要特征是弱酸性部位或表面硅烷醇基团。 FTIR曲线显示Bi-SBA-15处铋附近的富羟基表面(Bi / Si = 1/100)。基于催化剂的表征和活性数据的相关性,可以认为肟酸氧的质子化可以由路易斯酸中心铋附近的表面硅烷醇引发。己内酯的高时空产率为114.3 mol g(cat)(-1)h(-1)。 (C)2015 Elsevier B.V.保留所有权利。

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