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FISGHER-TROPSCH SYNTHESIS: HIGH OXYGENATE SELECTIVITY OF HYDORTHERMAL CARBON SUPPORTED COBALT CATALYSTS

机译:表面滴合成:高含氧化合物的硫代甲基碳负载钴催化剂

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Synthesis gas, a mixture of carbon monoxide and hydrogen (H2/CO) can be converted into hydrocarbons using cobalt (Co) catalysts during Fischer Tropsch Synthesis (FTS). Cobalt is well known for its activity in FTS and is typically supported on metal oxides, chiefly Al2O3 or SiO2. Extensive efforts have been made to develop FTS catalysts with high activity and high C_(5+) selectivity [1,2] and the prospect of using ordered porous carbon materials as support for Co catalysts was previously introduced to minimize or even by-pass the catalyst-support-interactions typically encountered for small cobalt particles [3]. Carbon support structures have been shown to influence the reactivity and product distribution during FTS and for Co catalysts the activities for various mesoporous carbon supports were previously assessed [4]. Carbon support structures are an appealing alternative to metal oxides since the surfaces can be manipulated with appropriate surface functionalization and surface areas can be enhanced through physical and chemical treatments [5]. However, there are great variations in carbon support materials including fibers, nanotubes, nanowires and molecular sieves, just to mention a few, and they may produce many different outcomes for FTS [6]. The current study focuses on hydrothermally-derived carbon spheres as a support for Co nanoparticles. Carbonaceous materials made from the hydrothermal process are unique in that properties such as microstructure, surface functionality, size, morphology, chemical composition, surface area and micro- and meso-porosity can be tailored by the selection of the carbohydrate precursor and synthetic growth conditions. The hydrothermal synthesis (HTS) process for generating carbonaceous materials in the form of nano- and microspheres can use mono- and polysaccharides
机译:合成气,可以在费 - 托托合成(FTS)期间使用钴(CO)催化剂将一氧化碳和氢气(H2 / CO)的混合物转化为烃基。钴以其FTS的活性众所周知,通常在金属氧化物上负载,主要是Al 2 O 3或SiO 2。已经进行了广泛的努力,以高活性和高C_(5+)选择性[1,2]和使用有序多孔碳材料作为对CO催化剂的载体的前景,以最小化甚至通过通过通常遇到用于小钴颗粒的催化剂 - 载体相互作用[3]。已显示碳载体结构以影响FTS期间的反应性和产品分布,并且对于CO催化剂,先前评估了各种介孔碳载体的活性[4]。碳载体结构是一种吸引金属氧化物的替代方案,因为表面可以用适当的表面官能化操纵,并且通过物理和化学处理可以提高表面积[5]。然而,碳载体材料存在很大的变化,包括纤维,纳米管,纳米线和分子筛,只是提及一些,它们可以为FTS产生许多不同的结果[6]。目前研究重点介绍了水热源衍生的碳球作为CO纳米颗粒的载体。通过选择碳水化合物前体和合成生长条件,可以通过选择微观结构,表面功能,尺寸,形态,化学组合物,表面积和微孔和微孔隙等性质,所述碳质材料是独一无二的。用于产生纳米和微球形式的水热合成(HTS)方法可以使用单糖和多糖

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