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Catalytic performance of Iron-based catalyst in Fischer-Tropsch synthesis using CO2 containing syngas

机译:使用Syngas的CO2催化铁基催化剂在Fischer-Tropsch合成中的催化性能

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This paper focuses on the catalytic performance of iron-based catalyst in Fischer-Tropsch Synthesis (FTS) using CO2 containing syngas. The catalysts were prepared by incipient wetness impregnation method of silica with solution of iron nitrate followed by calcination in air. Physical and chemical properties of iron-based catalyst were carried out using N2 adsorption-desorption, H2-TPR, CO-TPR and TPH. The catalysts were tested in Fischer-Tropsch conditions (T = 220°C, P = 1 bar, GHSV = 300 h~(-1), H2/CO_x = 0.5). The results show that iron-based catalyst activated by CO is more active for hydrogenation than the catalyst activated by H2. The activation of iron-based catalyst by CO provides iron carbide combining with iron oxide which was reduced partially. Fe3O4 (partial reduced iron oxide) is expected to be exist in the iron-based catalyst pretreated by CO. This oxide phase allows the conversion of CO2 to CO through the reverse water-gas-shift (RWGS) reaction. Thus, iron-based catalyst activated by CO is a candidate catalyst for FTS using CO2 containing syngas. Fe3O4 enhances RWGS activity while iron carbide is effective for the hydrogenation. The different product distributions of H2-CO, H2-CO2 and H2-CO-CO2 mixtures are due to the different reaction pathway of CO and CO2. The key of reaction pathway is the active site generated from pretreatment method.
机译:本文侧重于使用CO 2含有合成气的Fischer-Tropsch合成(FTS)中铁基催化剂的催化性能。通过二氧化硅的初期湿润浸渍方法使用二氧化硅的溶液和硝酸铁溶液制备催化剂,然后在空气中进行煅烧。使用N 2吸附 - 解吸,H2-TPR,CO-TPR和TPH进行铁基催化剂的物理和化学性质。在Fischer-Tropsch条件下测试催化剂(T = 220℃,P = 1巴,GHSV = 300h〜(-1),H2 / CO_X = 0.5)。结果表明,由CO激活的铁基催化剂比由H 2活化的催化剂更活跃。 CO通过CO的铁基催化剂的激活提供与部分减少的氧化铁组合的碳化铁。预期Fe3O4(部分还原的氧化铁)在CO的铁基催化剂中存在。该氧化物相可以通过反向水 - 气体移(RWGS)反应转化CO 2。因此,由CO活化的铁基催化剂是使用含有CO 2的FTS的候选催化剂。 Fe3O4增强了rwgs活性,而碳化铁对氢化有效。 H 2-CO,H 2 -CO2和H 2-CO2混合物的不同产品分布是由于CO和CO2的不同反应途径。反应途径的关键是从预处理方法产生的活性位点。

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