Green catalyst innovation: Enhanced Fischer-Tropsch synthesis using potassium-promoted cobalt catalysts supported on pyrolyzed peanut shells and Cladophora Glomerata modified biochars

IF 7.2 2区 工程技术 Q1 CHEMISTRY, APPLIED Fuel Processing Technology Pub Date : 2024-04-29 DOI:10.1016/j.fuproc.2024.108094
Fatemeh Bayat , S.M. Pirbazari , Nastaran Shojaei , Shiva Kiani , Ahmad Tavasoli
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Abstract

This paper explores pyrolysis potential for effective modified biochar (MB) production, serving as a green and novel carbon-based catalyst support in Fischer-Tropsch to olefins synthesis. For this purpose, the MB produced from the pyrolysis of pre-treated Peanut shell (PS) and Cladophora glomerata algae (CG) was used as a high porosity support for cobalt catalyst synthesis. The impregnation technique was applied to prepare the cobalt catalysts, and the catalysts were promoted with potassium. Various methods examine catalysts physico-chemical properties. After 10  h of reduction at 400 °C, the catalysts' activity and selectivity were studied in a fixed-bed reactor. TEM images show that the metal particles are suitably distributed on the porous surface of the modified biochars. The majority of the particles were between 5 and 15 nm in size. Also, TPR results indicate a suitable metal dispersion of about 10% and good catalyst reducibility have been achieved. The cobalt catalysts produced on MBs of CG and PS exhibited FT rates of 0.245 and 0.223 (g HC/g cat.h), with CO conversion rates of 50.25% and 45.68% in each case. Finally, K-promoted cobalt catalysts supported on MBs of CG and PS showed the α-olefins selectivities of 38.67% and 35.49% for C2-C13 hydrocarbons, respectively.

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绿色催化剂创新:使用支撑在热解花生壳和经改性生物秸秆上的钾促进钴催化剂强化费托合成
本文探讨了有效生产改性生物炭(MB)的热解潜力,将其作为费托合成烯烃过程中的绿色新型碳基催化剂载体。为此,预处理花生壳(PS)和藻类(CG)热解产生的生物炭被用作钴催化剂合成的高孔隙率载体。采用浸渍技术制备钴催化剂,并用钾对催化剂进行促进。采用多种方法检测催化剂的物理化学性质。在 400 °C 下还原 10 小时后,在固定床反应器中研究了催化剂的活性和选择性。TEM 图像显示,金属颗粒适当地分布在改性生物沥青的多孔表面上。大部分颗粒的大小在 5 至 15 纳米之间。此外,TPR 结果表明,金属分散度约为 10%,催化剂还原性良好。在 CG 和 PS 的 MBs 上生产的钴催化剂的 FT 率分别为 0.245 和 0.223(g HC/g cat.h),CO 转化率分别为 50.25% 和 45.68%。最后,以 CG 和 PS 甲基溴为载体的 K 促进钴催化剂对 C2-C13 碳氢化合物的 α-olefins 选择性分别为 38.67% 和 35.49%。
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来源期刊
Fuel Processing Technology
Fuel Processing Technology 工程技术-工程:化工
CiteScore
13.20
自引率
9.30%
发文量
398
审稿时长
26 days
期刊介绍: Fuel Processing Technology (FPT) deals with the scientific and technological aspects of converting fossil and renewable resources to clean fuels, value-added chemicals, fuel-related advanced carbon materials and by-products. In addition to the traditional non-nuclear fossil fuels, biomass and wastes, papers on the integration of renewables such as solar and wind energy and energy storage into the fuel processing processes, as well as papers on the production and conversion of non-carbon-containing fuels such as hydrogen and ammonia, are also welcome. While chemical conversion is emphasized, papers on advanced physical conversion processes are also considered for publication in FPT. Papers on the fundamental aspects of fuel structure and properties will also be considered.
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