双金属Na-Fe0.9Mg0.1Ox上直接CO2加氢合成长链石蜡

IF 2.8 3区 化学 Q2 CHEMISTRY, APPLIED Topics in Catalysis Pub Date : 2023-11-28 DOI:10.1007/s11244-023-01888-3
Sheraz Ahmed, Syeda Sidra Bibi, Muhammad Irshad, Muhammad Asif, Muhammad Kashif Khan, Jaehoon Kim
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引用次数: 0

摘要

在铁催化剂上直接将二氧化碳加氢成长链碳氢化合物被认为是缓解全球变暖问题最有希望的方法。然而,铁催化剂通常会产生富含烯烃的碳氢化合物,这使得它们很难直接用作液体运输燃料。本文提出了一种双金属Na-Fe0.9Mg0.1Ox催化剂,该催化剂可生成富含石蜡的长链烃,C5+产率高达17.9%,CO2转化率高达42.1%。催化剂表面氧空位的形成和电子从MgO到Fe相的转移提高了Fe3O4对α-Fe的还原性。此外,MgO的存在增加了H2和CO2的吸附,促进了C-C偶联反应生成长链烷烃。Fe0.9Mg0.1Ox具有CO2转化率高、C5+产率高、产物石蜡丰富等特点,是工业条件下生产液体运输燃料极具前景的催化剂。
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Synthesis of Long-chain Paraffins over Bimetallic Na–Fe0.9Mg0.1Ox by Direct CO2 Hydrogenation

Direct CO2 hydrogenation into long-chain hydrocarbons over iron catalysts is considered the most promising approach to mitigate global warming issues. However, iron catalysts typically produce olefin-rich hydrocarbons, which make it difficult to directly use them as liquid transportation fuels. Here, we present a bimetallic Na–Fe0.9Mg0.1Ox catalyst that produced paraffin-rich long-chain hydrocarbons with a high C5+ yield of 17.9% at a high CO2 conversion of 42.1%. The formation of oxygen vacant sites at the catalyst surface and electron transfer from MgO to Fe phase increased the reducibility of Fe3O4 to α–Fe. In addition, the presence of MgO increased the H2 and CO2 adsorption and facilitated the C–C coupling reaction to produce long-chain paraffins. The high CO2 conversion, high C5+ yield, and paraffin-rich products make Fe0.9Mg0.1Ox a highly promising catalyst to produce liquid transportation fuels under industry-relevant conditions.

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来源期刊
Topics in Catalysis
Topics in Catalysis 化学-物理化学
CiteScore
5.70
自引率
5.60%
发文量
197
审稿时长
2 months
期刊介绍: Topics in Catalysis publishes topical collections in all fields of catalysis which are composed only of invited articles from leading authors. The journal documents today’s emerging and critical trends in all branches of catalysis. Each themed issue is organized by renowned Guest Editors in collaboration with the Editors-in-Chief. Proposals for new topics are welcome and should be submitted directly to the Editors-in-Chief. The publication of individual uninvited original research articles can be sent to our sister journal Catalysis Letters. This journal aims for rapid publication of high-impact original research articles in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis.
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