Highly efficient separation and equilibrium recovery of H2/CO2 in hydrate-based pre-combustion CO2 capture

笼状水合物 水合物 燃烧 硅胶 多孔介质 润湿 气体分离 化学 化学工程 多孔性 二氧化碳 色谱法 有机化学 生物化学 工程类
作者
Yunseok Lee,Seungin Lee,Dongju Seo,Seokyoon Moon,Yun‐Ho Ahn,Youngjune Park
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:481: 148709-148709 被引量:13
标识
DOI:10.1016/j.cej.2024.148709
摘要

Gas hydrate-based CO2 capture processes have attracted considerable attention due to their potentials for energy-efficient pre-combustion CO2 capture. Recent investigations have explored the use of tailored-wettability porous silica gels, highlighting benefits in thermodynamic and kinetic efficiencies, specifically characterized by low energy requirements and rapid formation. However, achieving high purity levels for both H2 and CO2 is crucial for practical implementation. Consequently, identifying and optimizing an effective separation route becomes imperative. In this study, we examined the thermodynamic stability, gas uptake, and separation factors of THF (5.56 mol%) + H2 + CO2 hydrates with varying compositions (H2:CO2 = 80:20, 60:40, 30:70, or 20:80 mol%) in C0 and C1 silica gel (functionalized by monofunctional alkylsilanes (X-(CH3)2-Si-Cn)) systems with SDS (0 or 500 ppm). Pressure-composition diagrams for THF + H2 + CO2 systems in C0 and C1 silica gel were meticulously measured. Notably, the C1 silica gel system without SDS demonstrated good thermodynamic stability, substantial gas uptake, and a significant separation factor. Based on the pressure-composition diagram of the C1 silica gel system, we proposed a highly efficient route for separating H2 and CO2. This proposed cyclic process involves a three-stage reactor and achieve to gas hydrate-based pre-combustion CO2 capture, yielding a purity of approximately 91 % H2 and 94 % CO2. The present findings provide valuable insights into optimizing the wettability of porous media and efficient separation routes, demonstrating the feasibility of a gas hydrate-based pre-combustion carbon dioxide capture process.
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