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A Comparison study of NiW and NiPW hydrodesulfurization catalysts supported on SBA-15 and alumina

机译:SBA-15和氧化铝支持NiW和NIPW加氢脱硫催化剂的比较研究

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A series of Ni-promoted W HDS catalysts supported on SBA-15 or γ-alumina was prepared using two different active phase precursors, Keggin-type heteropolyacid, H3PW_(12)O_(40) (HPW), and ammonium metatungstate. Prepared catalysts were characterized by N2 physisorption, small- and wide-angle XRD, UV-Vis DRS, FT-IR, TPR, ~(31)P MAS-NMR, HRTEM and evaluated in hydrodesulfurization (HDS) of 4,6-dimethyldibenzothiophene (4,6-DMDBT). It was found that Keggin structure is preserved in the oxide precursor supported on SBA-15, whereas it is partially destroyed on γ-Al2O3 due to the strong interaction of parent HPW with this support. The catalysts supported on SBA-15 showed better catalytic performance than those supported on γ-alumina and the use of heteropolyacid precursor resulted in a further increase in catalytic activity. NiPW/SBA-15 catalyst showed the highest activity in 4,6-DMDBT HDS and an enhancement of the HYD route, which were attributed to the good dispersion and the appropriate morphology of the WS2 active phase.
机译:一系列支撑在SBA-15或γ氧化铝的Ni-促进W¯¯HDS催化剂的使用两种不同的活性相前体,Keggin型杂多酸,H3PW_(12)O_(40)(HPW),和偏钨酸铵制备。制备的催化剂是由N2物理吸附,小型和广角X射线衍射,紫外 - 可见DRS,FT-IR,TPR,〜(31)p MAS-NMR,HRTEM 4,6-二甲基的(HDS),其特征在于和加氢脱硫评价(4,6-DMDBT)。据发现,Keggin结构在支撑在SBA-15的氧化物前体由于父HPW与此支持强相互作用保留,而它被部分上γ-Al2O3的破坏。支持SBA-15催化剂表现出比那些支持γ氧化铝和使用杂多酸前体的更好的催化性能导致催化活性的进一步增加。 NiPW / SBA-15催化剂表现出4,6-DMDBT HDS活性最高和HYD的路线,这归因于良好的分散性和WS2活性相的适当形态的增强。

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