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NICKEL BASED CATALYSTS FOR SELECTIVE HYDROGENATION OF CINNAMALDEHYDE- INFLUENCE OF SUPPORT PHASES

机译:镍基肉桂醛选择性加氢的催化剂-支持相的影响

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摘要

Ni (15% w/w) supported on alumina, silica and titania (P-25, anatase and rutile phases) have been investigated for the liquid phase hydrogenation of cinnamaldehyde. XRD, TPR and XPS data (binding energy shifts for Ni 2p ) indicate metal-support interactions in all supported catalysts. Weaker bonding of H 2 on Ni/TiO 2 (H 2 -TPD) improves activity. Ni/TiO 2 phases display higher cinnamaldehyde conversion and selectivity to cinnamyl alcohol compared to the catalysts supported on alumina and silica. Amongst the three polymorphs of titania, the maximum activity and selectivity displayed by Ni/ TiO 2 -P-25, is attributed to the active Ni crystallites located at the interface between anatase and rutile phases in titania P-25 matrix (HRTEM). Though Ni crystallites on alumina and silica are relatively smaller (compared to those on the three TiO2 phases) in size, their activity vis-à-vis for those supported on titania phases is less, implying that factors other than crystallite size influence the performance.
机译:已经研究了负载在氧化铝,二氧化硅和二氧化钛(P-25,锐钛矿和金红石相)上的Ni(15%w / w)用于肉桂醛的液相加氢。 XRD,TPR和XPS数据(Ni 2p的结合能移动)表明在所有负载型催化剂中金属与载体之间的相互作用。 H 2在Ni / TiO 2(H 2 -TPD)上的弱结合提高了活性。与负载在氧化铝和二氧化硅上的催化剂相比,Ni / TiO 2相显示出更高的肉桂醛转化率和对肉桂醇的选择性。在二氧化钛的三种多晶型物中,Ni / TiO 2 -P-25显示的最大活性和选择性归因于位于二氧化钛P-25基质(HRTEM)中的锐钛矿相和金红石相之间的界面的活性Ni微晶。尽管在氧化铝和二氧化硅上的镍微晶尺寸相对较小(与三个TiO2相相比),但其对二氧化钛相负载的活性却相对较小,这表明除晶粒尺寸以外的其他因素也会影响性能。

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