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On the Preparation of Low Temperature Iron Fischer-Tropsch Catalysts: Strategies That Work and Those That Do Not

机译:在低温铁型鼠催化剂的制备:工作的策略和不这样做的策略

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Iron-based Fisher-Tropsch (FeFT) catalysts have a number of advantages over cobalt-based catalysts that make them attractive in the Biomass to Liquids (BTL) arena. This includes their ability to operate optimally with syngas of H_2/CO≤1.5. Historically, Low Temperature FeFT (LTFeFT) catalysts have been prepared by precipitating a copper-doped iron (hydr)oxide from a copper-containing iron nitrate solution. A major drawback of this preparation route is the resulting large quantity of nitrate-rich waste water. Recently, an approach utilizing carboxylic acids was proposed to overcome many of the environmental problems associated with the preparation of LTFeFT catalysts. Although promising, no FT performance data for catalysts prepared according to the organic acid method have been reported. We compared the performance of FT catalysts prepared according to the historical procedure and variants thereof with that of catalysts prepared according to the organic acid method. The catalysts prepared via the historical route exhibited superior surface area, pore volume and FT activity compared to those prepared via the carboxylic route. Fundamental principles of aqueous solution chemistry and precipitation theory provide an explanation for these differences.
机译:铁基捕捞(FeFT)催化剂具有与基于钴的催化剂的许多优点,使它们在生物质中具有吸引力至液体(BTL)竞技场。这包括它们与H_2 /Co≤1.5的合成气最佳地操作的能力。历史上,通过从含铜铁硝酸盐溶液沉淀铜掺杂的铁(氢)氧化物来制备低温FeFt(LTFeft)催化剂。该制备途径的主要缺点是由此产生大量富含硝酸盐的废水。最近,提出了一种利用羧酸的方法来克服与制备LTFeft催化剂相关的许多环境问题。虽然有希望,但已经报道了根据有机酸法制备的催化剂的FT性能数据。我们比较了根据历史程序和其变体制备的FT催化剂的性能与根据有机酸法制备的催化剂的催化剂。通过历史途径制备的催化剂与通过羧酸途径制备的那些表现出优异的表面积,孔体积和FT活性。水溶液化学和降水理论的基本原理提供了对这些差异的解释。

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