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Selective hydrogenation of phenylacetylene over bimetallic Pd-Cu/Al2O3 and Pd-Zn/Al2O3 catalysts

机译:在双金属Pd-Cu / Al2O3和Pd-Zn / Al2O3催化剂上苯乙炔的选择性加氢

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Bimetallic Pd-Cu/Al2O3 and Pd-Zn/Al2O3 catalysts with various Cu/Pd and Zn/Pd molar ratios were prepared and applied to the selective hydrogenation of phenylacetylene to styrene. The structure properties of the bimetallic catalysts were characterized by inductively coupled plasma-optical emission spectroscopy (ICP-OES), CO chemisorption, high-resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS). Different from Pd-Cu/Al2O3 where the interaction between Pd and Cu only generated the geometric effect, both geometric and electronic effects were observed for Pd-Zn/Al2O3. The activity and selectivity of the bimetallic catalysts can be tuned by varying the Cu/Pd and Zn/Pd molar ratios, which were essentially determined by the geometric and electronic effects of the catalysts. Although both Pd-Cu/Al2O3 and Pd-Zn/Al2O3 exhibited improved selectivity to styrene compared to monometallic Pd/Al2O3, there is a difference in the activity and selectivity between the two types of bimetallic catalysts at the same Cu/Pd and Zn/Pd molar ratio, which is mainly caused by the different modification degrees of Cu and Zn on Pd. Among all the catalysts prepared in this work, the Pd-Zn/Al2O3 with a Zn/Pd molar ratio of 6 displayed the best selectivity to styrene, being 86.3% at 99.5% phenylacetylene conversion. (C) 2015 Elsevier B.V. All rights reserved.
机译:制备了具有不同Cu / Pd和Zn / Pd摩尔比的双金属Pd-Cu / Al2O3和Pd-Zn / Al2O3催化剂,并将其用于苯乙炔选择性加氢制苯乙烯。通过电感耦合等离子体发射光谱法(ICP-OES),CO化学吸附,高分辨率透射电子显微镜(HRTEM)和X射线光电子能谱(XPS)表征了双金属催化剂的结构性能。与Pd-Cu / Al2O3的Pd-Cu相互作用仅产生几何效应不同,Pd-Zn / Al2O3的几何效应和电子效应均得到观察。可以通过改变Cu / Pd和Zn / Pd的摩尔比来调节双金属催化剂的活性和选择性,这主要是由催化剂的几何和电子效应决定的。尽管与单金属Pd / Al2O3相比,Pd-Cu / Al2O3和Pd-Zn / Al2O3均表现出对苯乙烯的提高的选择性,但在相同的Cu / Pd和Zn /下,两种类型的双金属催化剂的活性和选择性有所不同。 Pd摩尔比主要是由于Cu和Zn对Pd的改性程度不同所致。在这项工作中制备的所有催化剂中,Zn / Pd摩尔比为6的Pd-Zn / Al2O3显示出最佳的苯乙烯选择性,在99.5%的苯乙炔转化率下为86.3%。 (C)2015 Elsevier B.V.保留所有权利。

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