Tailoring CO2/CH4 Separation Efficiency with [THTDP][Cl]/Pebax-1657 Supported Ionic Liquid Membranes: Design, Characterization, and Theoretical Insights

IF 2.8 3区 化学 Q2 CHEMISTRY, APPLIED Topics in Catalysis Pub Date : 2024-06-20 DOI:10.1007/s11244-024-01978-w
Tushar Patil, Sarthak Patel, Manish Kumar Sinha, Swapnil Dharaskar, Jalaja Pandya, Satyam Shinde, Mika Sillanpaa, Chang Yoo, Mohammad Khalid
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Abstract

The use of renewable resources to generate energy is growing, but regrettably, the large amount of CO2 emissions it releases harms the environment. The main greenhouse gas, CO2, is a major factor in global climate change, which eventually disrupts the delicate balance of ecosystems within the globe. Therefore, the development of effective and sustainable technology for CO2 capture and storage is both urgent and compelling. Among many different approaches for CO2 capture, membrane separation has shown to be one of the most promising, yielding excellent results in terms of effectiveness as well as affordability. Nonetheless, to enhance membrane performance more significantly in CO2 separation, researchers have focused on ionic liquids, a family of organic salts recognized for their high thermal stability, low volatility, and tuneable characteristics. Because of this, ionic liquids have attracted a lot of attention from the academic and industrial sectors as possible additions to enhance membranes’ capacity for CO2 separation. This study explores the potential of Tetrahexyl tetradecyl phosphonium chloride incorporated into Pebax-1657 to enhance CO2/CH4 separation performance. Ion gel membranes were synthesized with varying ionic liquid concentrations (5, 10, 20 wt%) and characterized for structural and morphological evaluations. Gas separation performance was assessed through permeation experiments, showing increased CO2/CH4 selectivity from 19.23 to 21.81 with higher IL concentrations, especially under high pressure. CO2 permeability increased from 70.01 to 273.61 barrer with the addition of 20% [THTDP][Cl]. Density functional theory calculations provided theoretical insights into the interaction energies between ionic liquid and gas molecules, corroborating experimental findings. The study demonstrates the novelty of integrating phosphonium-based ionic liquid with Pebax-1657, significantly enhancing CO2/CH4 selectivity due to strong CO2 interactions. This research offers a promising approach to developing advanced membranes for efficient and selective CO2 capture, contributing to sustainable gas separation technologies.

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利用[THTDP][Cl]/Pebax-1657 支持离子液体膜定制 CO2/CH4 分离效率:设计、表征和理论见解
利用可再生资源生产能源的现象越来越多,但令人遗憾的是,它所排放的大量二氧化碳会对环境造成危害。主要温室气体二氧化碳是导致全球气候变化的主要因素,最终会破坏全球生态系统的微妙平衡。因此,开发有效、可持续的二氧化碳捕集与封存技术既迫切又必要。在许多不同的二氧化碳捕获方法中,膜分离是最有前途的方法之一,在有效性和经济性方面都取得了卓越的成果。然而,为了更显著地提高膜在二氧化碳分离中的性能,研究人员把重点放在了离子液体上。离子液体是一种有机盐类,因其具有高热稳定性、低挥发性和可调节的特性而被公认。正因为如此,离子液体作为增强膜的二氧化碳分离能力的可能添加物,吸引了学术界和工业界的大量关注。本研究探讨了在 Pebax-1657 中加入四己基十四烷基氯化鏻以提高 CO2/CH4 分离性能的潜力。研究人员合成了不同离子液体浓度(5、10、20 wt%)的离子凝胶膜,并对其结构和形态进行了评估。通过渗透实验评估了气体分离性能,结果表明随着离子液体浓度的增加,二氧化碳/四氯化碳的选择性从 19.23 增加到 21.81,尤其是在高压条件下。加入 20% [THTDP][Cl]后,二氧化碳渗透率从 70.01barrer 增加到 273.61barrer。密度泛函理论计算从理论上揭示了离子液体和气体分子之间的相互作用能量,证实了实验结果。该研究证明了将鏻基离子液体与 Pebax-1657 结合在一起的新颖性,由于二氧化碳的强相互作用,大大提高了 CO2/CH4 的选择性。这项研究为开发用于高效和选择性捕获二氧化碳的先进膜提供了一种前景广阔的方法,有助于可持续气体分离技术的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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