机构地区:[1]Institute of Catalysis, Department of Chemistry, Zhejiang University, Hangzhou 310028, China [2]College of Chemical and Material Engineering, Quzhou University, Quzhou 324000, China
出 处:《Journal of Zhejiang University-Science A(Applied Physics & Engineering)》2012年第5期395-406,共12页浙江大学学报(英文版)A辑(应用物理与工程)
基 金:supported by the National Natural Science Foundation of China (Nos. 21073159 and 90610002);the National Basic Research Program (973) of China (No. 2007CB210207);the Zhejiang Provincial Natural Science Foundation of China (No. Z406142)
摘 要:The synthesis of methanol and dimethyl ether(DME) from CO hydrogenation has been investigated on Cu-based catalysts.A series of Cu/ZnO/Al2O3 catalysts were prepared using a solvent-free routine which involved a direct blend of copper/zinc/aluminum salts and citric acid,followed by calcination at 450 °C.The calcination processes were monitored using thermogravimetry differential scanning calorimetry(TG-DSC).Catalysts were further characterized using N2 adsorption,scanning electronic microscopy(SEM),X-ray diffraction(XRD),N2O oxidation followed by H2 titration,and temperature-programmed reduction with H2(H2-TPR).The reduction processes were also monitored with in-situ XRD.The physicochemical properties of catalysts depended strongly on the types of precursor salts,and catalysts prepared using Al acetate and Cu nitrate as starting materials had a larger surface area,larger exposed metallic copper surface area,and lower reduction temperature.The CO hydrogenation performances of these catalysts were compared and discussed in terms of their structures.Catalysts prepared with copper nitrate,zinc and aluminum acetates exhibited the highest catalytic activity.The synthesis of methanol and dimethyl ether (DME) from CO hydrogenation has been investigated on Cu-based catalysts. A series of Cu/ZnO/AI203 catalysts were prepared using a solvent-free routine which involved a direct blend of copper/zinc/aluminum salts and citric acid, followed by calcination at 450 ~C. The calcination processes were monitored using thermogravimetry differential scanning calorimetry (TG-DSC). Catalysts were further characterized using N2 adsorption, scanning electronic microscopy (SEM), X-ray diffraction (XRD), N20 oxidation followed by H2 titration, and temperature-programmed reduction with H2 (HE-TPR). The reduction processes were also monitored with in-situ XRD. The physicochemical properties of catalysts depended strongly on the types of precursor salts, and catalysts prepared using A1 acetate and Cu nitrate as starting materials had a larger surface area, larger exposed metallic copper surface area, and lower reduction temperature. The CO hy- drogenation performances of these catalysts were compared and discussed in terms of their structures. Catalysts prepared with copper nitrate, zinc and aluminum acetates exhibited the highest catalytic activity.
关 键 词:Cu/ZnO/Al2O3 catalyst Solvent-free routine CO hydrogenation METHANOL Dimethyl ether
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