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Adsorption and reduction of nitrate in water on hydrotalcite-supported Pd-Cu catalyst

机译:水滑石负载钯铜催化剂对水中硝酸盐的吸附和还原

摘要

The hydrotalcite-supported Pd-Cu catalysts were successfully prepared by the impregnation or coprecipitation method, and their adsorption and catalytic reduction activity for nitrate in water were evaluated. The catalysts were characterized by X-ray diffraction (XRD) and surface area (BET) analysis. The results demonstrated that hydrotalcite-supported Pd-Cu catalysts could significantly adsorb nitrate ions, and then, effectively catalytically reduce them. The excellent adsorption ability for nitrate resulted from the regenerated layer structure of calcined hydrotalcite catalyst in nitrate aqueous solution. Nitrate was forced into the interlayer space and adsorbed on the external surface. The adsorption kinetics and the adsorption isotherm could be well described by pseudo-second-order model and the Langmuir model, respectively. The comparison of catalytic reduction with the adsorption for nitrate indicated that catalytic hydrogenation activity for nitrate increased with increasing adsorption capacity; nitrate reduction on hydrotalcite-supported Pd-Cu catalysts was a consecutive and dynamic adsorption and catalytic hydrogenation process. In addition, the catalyst obtained by coprecipitation method, with intact regeneration of hydrotalcite structure and a high dispersion of active metals, hold higher adsorption and catalytic activity than that prepared by co-impregnation method. (c) 2007 Elsevier B.V. All rights reseved.
机译:通过浸渍或共沉淀法成功制备了水滑石负载的Pd-Cu催化剂,并评价了其对水中硝酸盐的吸附和催化还原活性。通过X射线衍射(XRD)和表面积(BET)分析来表征催化剂。结果表明,水滑石负载的Pd-Cu催化剂可以显着吸附硝酸根离子,然后有效地催化还原它们。煅烧水滑石催化剂在硝酸盐水溶液中的再生层结构,使硝酸盐具有优异的吸附能力。硝酸盐被迫进入层间空间并吸附在外表面上。吸附动力学和吸附等温线可以分别用伪二级模型和Langmuir模型很好地描述。催化还原与硝酸盐吸附的比较表明,硝酸盐的催化加氢活性随吸附量的增加而增加。在水滑石负载的Pd-Cu催化剂上还原硝酸盐是一个连续的动态吸附和催化加氢过程。此外,与共浸渍法相比,通过共沉淀法获得的催化剂具有完整的水滑石结构再生和高活性金属分散性,具有更高的吸附和催化活性。 (c)2007 Elsevier B.V.保留所有权利。

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