二氧化碳捕集技术的多孔碳:揭示基础和创新

Surfaces Pub Date : 2023-09-18 DOI:10.3390/surfaces6030023
Gazi A. K. M. Rafiqul Bari, Jae-Ho Jeong
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引用次数: 0

摘要

多孔碳是一种新兴的材料,由于其高结构、机械和化学稳定性,以及可重复使用的优势,从排放的点源捕获二氧化碳。目前,研究工作主要集中在高压或中压吸附,而不是低压或DAC(直接空气捕获)条件。采用不同的活化合成途径,如硬模板、软模板、化学活化等,合成了含有杂原子(N、O等)的高多孔、功能化碳,在不同的温度和压力范围内实现了较高的CO2捕集效率。对不同活化途径下的基本孔隙形成机制进行了评价和探索。如果没有适当的CO2转移饱和扩散途径,光有更高的孔隙率是无效的。因此,必须强调更合理的宏/中/微/超/超孔隙多级设计策略,以提高这些孔隙的利用效率。此外,目前的研究主要集中在粉末基分层多孔碳材料上,这可能会降低捕获性能的效率,当将粉末塑造成颗粒或固定床形状时。因此,研究多孔碳颗粒的合成策略,探索其合成机理和捕集潜力是当务之急。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Porous Carbon for CO2 Capture Technology: Unveiling Fundamentals and Innovations
Porous carbon is an emerging material for the capture of CO2 from point sources of emissions due to its high structural, mechanical, and chemical stability, along with reusability advantages. Currently, research efforts are mainly focused on high- or medium-pressure adsorption, rather than low-pressure or DAC (direct air capture) conditions. Highly porous and functionalized carbon, containing heteroatoms (N, O, etc.), is synthesized using different activation synthesis routes, such as hard template, soft template, and chemical activation, to achieve high CO2 capture efficiency at various temperatures and pressure ranges. Fundamental pore formation mechanisms with different activation routes have been evaluated and explored. Higher porosity alone can be ineffective without the presence of proper saturated diffusion pathways for CO2 transfer. Therefore, it is imperative to emphasize more rational multi-hierarchical macro-/meso-/micro-/super-/ultra-pore design strategies to achieve a higher utilization efficiency of these pores. Moreover, the present research primarily focuses on powder-based hierarchical porous carbon materials, which may reduce the efficiency of the capture performance when shaping the powder into pellets or fixed-bed shapes for applications considered. Therefore, it is imperative to develop a synthesis strategy for pelletized porous carbon and to explore its mechanistic synthesis route and potential for CO2 capture.
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