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Unsupported trimetallic CoMoW sulfide HDS catalysts prepared by in situ decomposition of sulfur-containing precursors

机译:通过原位分解含硫前体制备的无载体三金属CoMoW硫化物HDS催化剂

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Unsupported CoMoW sulfide hydrodesulfurization (HDS) catalysts were prepared by in situ decomposition of sulfur-containing precursors. The precursors were synthesized by reaction of the ammonium and tetraalkylammonium thiomolybdotungstates (R4N)(4)MoWS8 (where R = H, methyl, propyl) with an aqueous solution of CoCl2 center dot 6H(2)O in order to give molar ratios of Co/[Co + (Mo + W)] = 0.3. Co-promoted precursors were then in situ decomposed during the HDS of dibenzothiophene (DBT)-producing CoMoW sulfide catalysts. Solids were analyzed after the in situ activation by scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction and for textural properties by using the BET and BJH methods. Catalysts with relatively high surface area and type IV N-2 adsorption-desorption isotherms were obtained. The use of the Co-promoted ammonium thiomolybdotungstate as precursor was found to be beneficial in the catalytic activity. The positive role of carbon in monometallic HDS catalysts confirmed by Chianelli and Berhault was not evidenced here since the catalytic activity decreased with the introduction of an alkyl group in the precursor. (C) 2014 Elsevier B.V. All rights reserved.
机译:通过原位分解含硫前体制备无载体的CoMoW硫化物加氢脱硫(HDS)催化剂。通过使铵盐和四烷基铵硫钼钼酸盐(R4N)(4)MoWS8(其中R = H,甲基,丙基)与CoCl2中心点6H(2)O的水溶液反应合成前驱体,以得到Co的摩尔比/ [Co +(Mo + W)] = 0.3。然后,在生产二苯并噻吩(DBT)的CoMoW硫化物催化剂的HDS过程中,将共助催化的前体原位分解。在原位活化后,通过扫描电子显微镜(SEM),高分辨率透射电子显微镜(HRTEM),X射线衍射对固体进行了分析,并使用BET和BJH方法对其结构进行了分析。获得了具有相对高表面积和IV N-2型吸附-吸附等温线的催化剂。发现使用共促进的硫代钼酸铵铵作为前体有利于催化活性。 Chianelli和Berhault证实了碳在单金属HDS催化剂中的积极作用,因为随着前体中烷基的引入,催化活性降低。 (C)2014 Elsevier B.V.保留所有权利。

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