高促进型Fe-Zn-Cu-K催化剂CO2费托合成性能研究

IF 4.8 2区 化学 Q2 CHEMISTRY, PHYSICAL
Beda Rolandi, Mattia Piacentini, Riccardo Ometto, Alessandro Porta, Carlo Giorgio Visconti
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引用次数: 0

摘要

比较了最先进的100Fe:10Zn:1Cu:4 K催化剂和Cu、K负载较高的催化剂在CO2费托合成中的活性、选择性和稳定性。较高的促进剂负载增加了对较重碳氢化合物的选择性,对高转化条件下的活性影响较小。在这种条件下,两种催化剂样品的活性损失可能是由于高水分压下的碳化铁氧化,但最先进的催化剂的选择性也受到影响,高度促进的催化剂保留了重产物的选择性。值得注意的是,在CO2/H2流动下,通过降低压力和提高温度,高促进催化剂可以成功地原位再生。这一过程几乎可以完全恢复初始活性,同时保持良好的C2+碳氢化合物选择性。相反,传统的费托催化剂,经过同样的回春处理后,表现出更明显的选择性转向更轻的产物。这些发现有助于制定稳定的催化剂,促进在工业相关条件下由二氧化碳一锅合成长链碳氢化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
On the performances of highly promoted Fe-Zn-Cu-K catalysts for CO2 Fischer-Tropsch synthesis
A state-of-the-art Fischer-Tropsch 100Fe:10Zn:1Cu:4 K catalyst and catalysts promoted with higher Cu and K loadings were compared in terms of activity, selectivity and stability in the CO2 Fischer-Tropsch synthesis. Higher promoter loadings increased selectivity towards heavier hydrocarbons, with a minor impact on activity at high conversion conditions. In such conditions, both catalysts samples experienced activity loss possibly due to iron carbide oxidation at high water partial pressure, but while the state-of-the-art catalyst had also selectivity affected, the highly promoted catalyst preserved heavy products selectivity. Notably, the highly promoted catalyst could be successfully rejuvenated in-situ by decreasing pressure and increasing temperature under CO2/H2 flow. This procedure allowed to restore almost completely the initial activity while preserving an excellent C2+ hydrocarbon selectivity. On the contrary, the traditional Fischer-Tropsch catalyst, after the same rejuvenation treatment, showed a more pronounced selectivity shift towards lighter products. These findings can help in formulating stable catalysts that promote the one-pot synthesis of long chain hydrocarbons from CO2 at industrially relevant conditions.
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来源期刊
Applied Catalysis A: General
Applied Catalysis A: General 化学-环境科学
CiteScore
9.00
自引率
5.50%
发文量
415
审稿时长
24 days
期刊介绍: Applied Catalysis A: General publishes original papers on all aspects of catalysis of basic and practical interest to chemical scientists in both industrial and academic fields, with an emphasis onnew understanding of catalysts and catalytic reactions, new catalytic materials, new techniques, and new processes, especially those that have potential practical implications. Papers that report results of a thorough study or optimization of systems or processes that are well understood, widely studied, or minor variations of known ones are discouraged. Authors should include statements in a separate section "Justification for Publication" of how the manuscript fits the scope of the journal in the cover letter to the editors. Submissions without such justification will be rejected without review.
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