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无铂和含铂催化剂用于甲烷光热干重整:综述

Photo-Thermal Dry Reforming of Methane with PGM-Free and PGM-Based Catalysts: A Review.

作者信息

Varotto Alessio, Pasqual Laverdura Umberto, Feroci Marta, Grilli Maria Luisa

机构信息

Energy Technologies and Renewable Sources Department, Italian National Agency for New Technologies, Energy and Sustainable Economic Development (ENEA), Via Anguillarese 301, 00123 Rome, Italy.

Department of Fundamental and Applied Sciences for Engineering (SBAI), Sapienza University of Rome, Via Castro Laurenziano, 7, 00161 Rome, Italy.

出版信息

Materials (Basel). 2024 Aug 1;17(15):3809. doi: 10.3390/ma17153809.

DOI:10.3390/ma17153809
PMID:39124473
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11312950/
Abstract

Dry reforming of methane (DRM) is considered one of the most promising technologies for efficient greenhouse gas management thanks to the fact that through this reaction, it is possible to reduce CO and CH to obtain syngas, a mixture of H and CO, with a suitable ratio for the Fischer-Tropsch production of long-chain hydrocarbons. Two other main processes can yield H from CH, i.e., Steam Reforming of Methane (SRM) and Partial Oxidation of Methane (POM), even though, not having CO as a reagent, they are considered less green. Recently, scientists' challenge is to overcome the many drawbacks of DRM reactions, i.e., the use of precious metal-based catalysts, the high temperatures of the process, metal particle sintering and carbon deposition on the catalysts' surfaces. To overcome these issues, one proposed solution is to implement photo-thermal dry reforming of methane in which irradiation with light is used in combination with heating to improve the efficiency of the process. In this paper, we review the work of several groups aiming to investigate the pivotal promoting role of light radiation in DRM. Focus is also placed on the catalysts' design and the progress needed for bringing DRM to an industrial scale.

摘要

由于通过该反应可以将一氧化碳和甲烷转化为合成气(一种氢气和一氧化碳的混合物,其比例适合费托合成生产长链烃),甲烷干重整(DRM)被认为是高效温室气体管理最有前景的技术之一。甲烷转化制氢还有另外两个主要过程,即甲烷蒸汽重整(SRM)和甲烷部分氧化(POM),不过,由于它们不使用一氧化碳作为反应物,所以被认为绿色程度较低。最近,科学家面临的挑战是克服DRM反应的诸多缺点,即使用贵金属基催化剂、该过程的高温、金属颗粒烧结以及催化剂表面的积碳。为克服这些问题,一种提出的解决方案是实施甲烷光热干重整,其中将光照射与加热结合使用以提高该过程的效率。在本文中,我们综述了几个研究小组旨在研究光辐射在DRM中的关键促进作用的工作。同时也关注催化剂的设计以及将DRM扩大到工业规模所需的进展。

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本文引用的文献

1
Facing Global Climate and Environmental Change.面对全球气候与环境变化
ACS Environ Au. 2023 May 17;3(3):121-122. doi: 10.1021/acsenvironau.3c00014.
2
Highly Efficient Solar-Driven Dry Reforming of Methane on a Rh/LaNiO Catalyst through a Light-induced Metal-To-Metal Charge Transfer Process.通过光诱导金属-金属电荷转移过程在Rh/LaNiO催化剂上实现高效太阳能驱动的甲烷干重整反应
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Photothermal Catalytic CO Conversion: Beyond Catalysis and Photocatalysis.
光热协同 CO 转化:超越催化和光催化。
Top Curr Chem (Cham). 2023 May 30;381(4):21. doi: 10.1007/s41061-023-00430-z.
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Thermo-photo catalysis: a whole greater than the sum of its parts.热光催化:整体大于部分之和。
Chem Soc Rev. 2022 May 10;51(9):3609-3647. doi: 10.1039/d1cs00782c.
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Accelerating photo-thermal CO reduction to CO, CH or methanol over metal/oxide semiconductor catalysts.在金属/氧化物半导体催化剂上加速光热将二氧化碳还原为一氧化碳、甲烷或甲醇。
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Light-Induced Redox Looping of a Rhodium/Ce WO Photocatalyst for Highly Active and Robust Dry Reforming of Methane.用于高活性和稳健甲烷干重整的铑/铈钨光催化剂的光诱导氧化还原循环
Angew Chem Int Ed Engl. 2022 May 16;61(21):e202200567. doi: 10.1002/anie.202200567. Epub 2022 Mar 23.
7
Indirect to Direct Charge Transfer Transition in Plasmon-Enabled CO Photoreduction.等离子体增强一氧化碳光还原中的间接到直接电荷转移跃迁
Adv Sci (Weinh). 2022 Jan;9(2):e2102978. doi: 10.1002/advs.202102978. Epub 2021 Nov 12.
8
Fundamentals and applications of photo-thermal catalysis.光热催化的基础与应用。
Chem Soc Rev. 2021 Feb 15;50(3):2173-2210. doi: 10.1039/d0cs00357c.
9
Photoassisted Selective Steam and Dry Reforming of Methane to Syngas Catalyzed by Rhodium-Vanadium Bimetallic Oxide Cluster Anions at Room Temperature.铑-钒双金属氧化物簇阴离子在室温下光辅助选择性催化甲烷蒸汽和干重整制合成气
Angew Chem Int Ed Engl. 2020 Nov 16;59(47):21216-21223. doi: 10.1002/anie.202010026. Epub 2020 Sep 11.
10
Visible-light-driven dry reforming of methane using a semiconductor-supported catalyst.使用半导体负载型催化剂的可见光驱动甲烷干重整
Chem Commun (Camb). 2020 Apr 28;56(33):4611-4614. doi: 10.1039/d0cc00729c. Epub 2020 Mar 25.