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Molybdocobaltate cobalt salts: New starting materials for hydrotreating catalysts

机译:钼酸二钴钴盐:加氢处理催化剂的新原料

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This paper deals with the use of Anderson heteropolyanions as alternative starting materials to the ammonium heptamolybdate and cobalt nitrate for the preparation of hydrotreatment oxidic precursors. Ammonium and cobalt salts of molybdocobaltate anions were synthesized and impregnated on alumina. The evolution of these compounds along the different steps of preparation of the oxidic precursors has been followed using various physical techniques such as Raman, XAS and UV-vis spectroscopies. It has been shown that the nature of the surface oxomolybdenum phase strongly depends on the nature of the starting salt. After sulfidation under H-2/H2S, the performances of these new catalysts have been evaluated in hydro&sulfuration of thiophene. It appears that the cobalt salt of the decamolybdocobaltate, anion [Co2Mo10O38H4](6-), with a Co/Mo ratio equal to 0.5, allows us to improve the catalytic conversion by comparison to reference catalysts prepared with ammonium heptamolybdate and cobalt nitrate as starting materials. It has been shown that this improvement is due to the preservation of the heteropolyanionic structure up to the drying step. (c) 2006 Elsevier B.V. All rights reserved.
机译:本文涉及使用安德森杂多阴离子作为七钼酸铵和硝酸钴的替代原料来制备加氢处理氧化前体。合成了钼二钴酸根阴离子的铵盐和钴盐并将其浸渍在氧化铝上。使用各种物理技术,例如拉曼光谱,XAS和紫外可见分光光度法,跟踪了这些化合物沿氧化前体制备不同步骤的演变。已经表明,表面氧钼相的性质很大程度上取决于起始盐的性质。在H-2 / H2S下硫化后,已在噻吩的加氢硫化中评估了这些新催化剂的性能。看起来十钴钼酸钴的钴盐阴离子[Co2Mo10O38H4](6-)的Co / Mo比等于0.5,与以七钼酸铵和硝酸钴为起始原料制备的参比催化剂相比,可以提高催化转化率。材料。已经表明,这种改进是由于直至干燥步骤都保留了杂多阴离子结构。 (c)2006 Elsevier B.V.保留所有权利。

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