Bimetallic Ni-Fe Supported by Gadolinium Doped Ceria (GDC) Catalyst for CO2 Methanation

Anis Kristiani, K. Takeishi, S. N. A. Jenie, H. T. Petrus
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Abstract

CO2 conversion into fuels and high value-added chemical feedstocks, such as methane, has gained novel interest as a crucial process for further manufacturing multi-carbon products. Methane, CH4, becomes a promising alternative for environmental and energy supply issues. Nickel-based catalysts were found to be very active and selective for CH4 production. The use of promoter and support material to develop high activity, high selectivity, and durable catalysts for CO2 methanation at low temperature is a challenge. Gadolinium-Doped Ceria (GDC) has been known as material for Solid Oxide Fuel Cell (SOFC) and Solid Oxide Electrolysis Cell (SOEC) due to higher ionic conductivity and lower operating temperatures. However, few researches have been done regarding to CO2 methanation over GDC as catalyst support so far. In this present work, CO2 methanation was investigated over bimetallic Ni-Fe catalyst supported by GDC. The results showed that CH4 production rate by using Ni-Fe/GDC catalyst was higher than that of GDC at all reaction temperatures carried on. Ni-Fe/GDC showed remarkable CH4 production rate as of 17.73 mmol.gcat−1.h−1 at 280 °C. No catalytic activity was produced by GDC catalyst only. The highest CO2 conversion (46.50%) was observed at 280 °C, with almost 100% selectivity to CH4. The turnover frequency (TOF) value of Ni-Fe/GDC (4529.32 h−1) was the highest than that of Ni and common CO2 methanation catalyst, Ni/Al2O3 catalysts at 280 °C, further displaying the outstanding low-temperature catalytic activity. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
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掺杂钆的铈 (GDC) 支持的双金属 Ni-Fe 催化剂用于二氧化碳甲烷化
将二氧化碳转化为燃料和高附加值化学原料(如甲烷)作为进一步生产多碳产品的关键工艺,已引起人们的新兴趣。甲烷(CH4)已成为解决环境和能源供应问题的有前途的替代品。研究发现,镍基催化剂对 CH4 的生产具有很高的活性和选择性。如何使用促进剂和支撑材料来开发高活性、高选择性和耐久性的催化剂,以便在低温条件下进行 CO2 甲烷化是一项挑战。掺钆铈(GDC)具有较高的离子传导性和较低的工作温度,因此一直被认为是固体氧化物燃料电池(SOFC)和固体氧化物电解电池(SOEC)的材料。然而,迄今为止,以 GDC 为催化剂载体进行二氧化碳甲烷化的研究还很少。本研究对以 GDC 为载体的双金属 Ni-Fe 催化剂进行了二氧化碳甲烷化研究。结果表明,在所有反应温度下,使用 Ni-Fe/GDC 催化剂的甲烷产生率均高于 GDC 催化剂。280 °C 时,Ni-Fe/GDC 的 CH4 产率高达 17.73 mmol.gcat-1.h-1。只有 GDC 催化剂没有催化活性。在 280 ℃ 时,二氧化碳转化率最高(46.50%),对 CH4 的选择性几乎达到 100%。在 280 °C时,Ni-Fe/GDC的翻转频率(TOF)值(4529.32 h-1)比Ni和普通二氧化碳甲烷化催化剂Ni/Al2O3催化剂的翻转频率(TOF)值最高,进一步显示了其出色的低温催化活性。作者版权所有 © 2024 年,BCREC 出版集团出版。本文采用 CC BY-SA 许可协议 (https://creativecommons.org/licenses/by-sa/4.0) 公开发表。
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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