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Synthesis and Characterisation of Co-based Fischer-Tropsch Catalysts and Supports, using hydrothermal and chemical attrition Method - The magnesium moderation Effect

机译:水热和化学磨损法合成和表征钴基费-托催化剂和载体-镁缓和作用

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摘要

Magnesium modification at different calcination temperatures of γ-alumina supports for cobalt Fischer-Tropsch catalysts was investigated. Support modification and catalyst preparation were performed by applying the incipient wetness impregnation method and resulted in supports containing 7,5 wt. % Mg and catalysts containing 12 wt. % Co and 0,5 wt. % Re. Selected support samples have in addition been promoted with 2 wt. % Al post magnesium modification, while others have been treated hydrothermally with water at 300 °C and 30 bar. The modified supports and the corresponding catalysts have been characterized by N2 adsorption, H2 chemisorption, X-ray diffraction and Fischer-Tropsch synthesis analysis in a dual isotherm fixed-bed unit at 20 bar, 210 ± 0,5 °C and H2/CO = 2,1.It was established that high temperature calcination of magnesium modified γ-alumina leads to a support material consisting of crystalline α-alumina and MgAl2O4 spinel.α-alumina formation was intensified by the addition of extra aluminium post magnesium impregnation. For the low temperature calcined magnesium modified γ-alumina supports only γ-alumina was detected, and for the medium temperature calcined supports only MgAl2O4 spinel was detected. Hydrothermal treatment with water appeared to induce boehmite formation in the magnesium modified support material. High temperature calcination led to low surface areas, small pore volumes and large pore diameters and magnesium modification does not have the ability to counteract this effect. High to medium temperature calcination resulted in larger surface areas, indicating that the collapse of pore structure to a certain degree is counteracted by introducing a 2-valent metal in the support material. A small decrease in surface area was observed upon addition of extra aluminium due to the initiating effect of extra aluminium addition to form α-alumina.Both the low temperature and the high temperature calcined magnesium modified alumina supported cobalt/rhenium catalyst were essentially inactive for the Fischer-Tropsch synthesis. The medium temperature calcined samples displayed relatively low activity as well.Increased C5+ selectivity was observed accompanying an increase in CO conversion and an increase in C5+ selectivity was observed upon magnesium modification of the γ-alumina support compared to the standard when MgAl2O4 spinel and/or α-alumina were present. The effect of increased surface acidity was an increase in C5+ selectivity at the expense of C4. It appears that magnesium moderation does not cause any changes in methane selectivity.
机译:研究了用于钴费-托催化剂的γ-氧化铝载体在不同煅烧温度下的镁改性。载体改性和催化剂的制备是通过采用初期湿润浸渍法进行的,得到的载体中含有7.5wt。 %的Mg和含有12wt。%的催化剂。 %Co和0.5 wt。 % 回覆。所选的支持物样品还用2 wt。镁改性后的Al含量为%,而其他Al则在300°C和30 bar的条件下用水进行水热处理。在20 bar,210±0.5°C和H2 / CO的双等温固定床装置中,通过N2吸附,H2化学吸附,X射线衍射和Fischer-Tropsch合成分析来表征改性载体和相应的催化剂= 2,1。已确定镁改性的γ-氧化铝的高温煅烧会导致由结晶α-氧化铝和MgAl2O4尖晶石组成的载体材料。镁浸渍后添加额外的铝可增强α-氧化铝的形成。对于低温煅烧的镁改性的γ-氧化铝载体,仅检测到γ-氧化铝,对于中温煅烧的载体,仅检测到MgAl2O4尖晶石。用水进行水热处理似乎在镁改性的载体材料中引起勃姆石的形成。高温煅烧导致表面积低,孔体积小和孔径大,并且镁改性不能抵消这种作用。高温至中温煅烧导致较大的表面积,这表明通过在载体材料中引入2价金属可在一定程度上抵消孔结构的崩溃。由于添加了额外的铝以形成α-氧化铝的引发作用,添加了额外的铝后发现表面积有小幅下降。低温和高温煅烧的镁改性氧化铝负载的钴/ r催化剂对催化剂基本上没有活性。费-托合成。与MgAl2O4尖晶石和/或MgAl2O4尖晶石相比,对γ-氧化铝载体进行镁改性后,观察到C5 +选择性增加,伴随着CO转化率的增加,C5 +选择性增加。存在α-氧化铝。增加表面酸度的作用是增加了C5 +的选择性,但以C4为代价。看来镁适量不会引起甲烷选择性的任何变化。

著录项

  • 作者

    Karlsen Aina Elin;

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  • 年度 2011
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  • 原文格式 PDF
  • 正文语种 eng
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