Fischer-Tropsch Synthesis on Co/SBA-15 Catalyst: Characterization and Oligomerization Modeling

V. Menezes, G. M. Paula, L. A. Lima, M. Rodrigues, F. Fernandes
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Abstract

In this study, we investigated the oligomerization mechanism of the Fischer-Tropsch synthesis catalyzed by a cobalt-based catalyst supported by SBA-15. The Co/SBA-15 catalyst contained 20% w/w of cobalt. It was prepared by the wet impregnation method and characterized by X-ray diffraction (XRD), N2 adsorption-desorption, temperature-programmed reduction (TPR), and scanning electron microscopy coupled to X-ray energy dispersion spectroscopy (SEM-EDS). The FT synthesis was conducted in a slurry bed reactor operating at 240–270°C, 2.0–3.0 MPa, and 1:1–2:1 H2:CO ratio (mol:mol). An oligomerization model, based on alkyl and alkenyl mechanisms for hydrocarbon chain propagation, was used for product distribution. Impregnation with cobalt and calcination did not alter the structure of SBA-15. Cobalt oxides, including Co2O3 and Co3O4, were the active phases of the reaction. Adding cobalt to the support lowered the specific surface area and the pore volume of the support but did not change the structure of SBA-15. Fischer-Tropsch synthesis and C5+ hydrocarbon selectivity increased at a low H2:CO ratio (1.0) and low temperatures (240–255°C). The content of branched-chain paraffin and olefins increased with a decrease in the H2:CO ratio and temperature. The parameters of the model were estimated, and the assumption of a dual mechanism was satisfied.
Co/SBA-15催化剂上的费托合成:表征和寡聚化模拟
在这项研究中,我们研究了SBA-15负载的钴基催化剂催化费托合成的寡聚化机理。Co/SBA-15催化剂的钴含量为20% w/w。采用湿浸渍法制备,通过x射线衍射(XRD)、N2吸附-解吸、程序升温还原(TPR)、扫描电镜- x射线能谱(SEM-EDS)等手段对其进行表征。在料浆床反应器中,在240 ~ 270℃,2.0 ~ 3.0 MPa, 1:1 ~ 2:1 H2:CO比(mol:mol)条件下合成FT。产品分布采用基于烷基和烯基机制的低聚化模型。钴浸渍和煅烧均未改变SBA-15的结构。Co2O3和Co3O4是反应的活性相。在支架中添加钴降低了支架的比表面积和孔隙体积,但没有改变SBA-15的结构。在较低的H2:CO比(1.0)和较低的温度(240 ~ 255℃)下,费托合成和C5+碳氢化合物选择性提高。支链烷烃和烯烃的含量随着H2:CO比和温度的降低而增加。对模型参数进行了估计,满足双机构的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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