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{"title":"Physicochemical synergistic adsorption of CO2 by PEI-impregnated hierarchical porous polymers","authors":"Lanxin Li, Zhibo Luo, Wei Zou, Shengke Liang, Hong Wang, Chen Zhang","doi":"10.1002/ghg.2263","DOIUrl":null,"url":null,"abstract":"<p>Amine-functionalized porous polymers have been considered as a prominent chemical adsorption material for carbon capture and storage (CCS) process, because of their large adsorption capacity and high selectivity. By comparison, the low energy-consumption for desorption and high recyclability are the advantages of the physical adsorption approach. In this work, an amine-functionalized hierarchical porous polymer was prepared by HIPE (high internal phase emulsions) template and amine impregnation strategy, and applied as CO<sub>2</sub> adsorbent to realize chemical adsorption and physical adsorption simultaneously. First, a hierarchical porous matrix of poly(styrene-glycidyl methacrylate) was prepared by the HIPE method. The formed meso/micropores in the typical porous polymer matrix could attract CO<sub>2</sub> molecules, where the physical adsorption was achieved. Subsequently, PEI (polyethyleneimine) was impregnated into the porous polymer with abundant macropores, and the numerous of amino groups provided the reaction sites, where the chemical adsorption was achieved. As a result, an effective CO<sub>2</sub> adsorption material was obtained via controlling the porous structure by changing the volume fraction of dispersive phase, impregnation condition and amine loading. Aided by the chemical adsorption of amino groups, the CO<sub>2</sub> adsorption capacity of the obtained adsorbent reached 3.029 mmol/g. Moreover, the CO<sub>2</sub> adsorption thermodynamics confirmed the physicochemical synergistic adsorption, and then the <i>Q</i><sub>st</sub> reduced to 31–42 kJ/mol and a good cyclic stability was obtained. As conclusion, the porous adsorbent showed a good industrial application prospect. © 2024 Society of Chemical Industry and John Wiley & Sons, Ltd.</p>","PeriodicalId":12796,"journal":{"name":"Greenhouse Gases: Science and Technology","volume":"14 2","pages":"270-283"},"PeriodicalIF":2.7000,"publicationDate":"2024-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Greenhouse Gases: Science and Technology","FirstCategoryId":"93","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ghg.2263","RegionNum":4,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
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Abstract
Amine-functionalized porous polymers have been considered as a prominent chemical adsorption material for carbon capture and storage (CCS) process, because of their large adsorption capacity and high selectivity. By comparison, the low energy-consumption for desorption and high recyclability are the advantages of the physical adsorption approach. In this work, an amine-functionalized hierarchical porous polymer was prepared by HIPE (high internal phase emulsions) template and amine impregnation strategy, and applied as CO2 adsorbent to realize chemical adsorption and physical adsorption simultaneously. First, a hierarchical porous matrix of poly(styrene-glycidyl methacrylate) was prepared by the HIPE method. The formed meso/micropores in the typical porous polymer matrix could attract CO2 molecules, where the physical adsorption was achieved. Subsequently, PEI (polyethyleneimine) was impregnated into the porous polymer with abundant macropores, and the numerous of amino groups provided the reaction sites, where the chemical adsorption was achieved. As a result, an effective CO2 adsorption material was obtained via controlling the porous structure by changing the volume fraction of dispersive phase, impregnation condition and amine loading. Aided by the chemical adsorption of amino groups, the CO2 adsorption capacity of the obtained adsorbent reached 3.029 mmol/g. Moreover, the CO2 adsorption thermodynamics confirmed the physicochemical synergistic adsorption, and then the Q st reduced to 31–42 kJ/mol and a good cyclic stability was obtained. As conclusion, the porous adsorbent showed a good industrial application prospect. © 2024 Society of Chemical Industry and John Wiley & Sons, Ltd.
聚乙烯醇浸渍分层多孔聚合物对二氧化碳的物理化学协同吸附作用
胺功能化多孔聚合物具有吸附容量大、选择性高的特点,因此被认为是碳捕集与封存(CCS)工艺中一种重要的化学吸附材料。相比之下,物理吸附法具有解吸能耗低、可回收性高等优点。本研究采用 HIPE(高内相乳化)模板和胺浸渍策略制备了胺功能化分层多孔聚合物,并将其用作二氧化碳吸附剂,同时实现了化学吸附和物理吸附。首先,采用 HIPE 法制备了聚苯乙烯-甲基丙烯酸缩水甘油酯的分层多孔基质。典型多孔聚合物基质中形成的中孔/微孔可以吸附二氧化碳分子,从而实现物理吸附。随后,PEI(聚乙烯亚胺)被浸渍到具有丰富大孔的多孔聚合物中,大量的氨基提供了反应位点,实现了化学吸附。因此,通过改变分散相的体积分数、浸渍条件和胺负载量来控制多孔结构,从而获得了一种有效的二氧化碳吸附材料。在氨基的化学吸附作用下,所得吸附剂的二氧化碳吸附容量达到了 3.029 mmol/g。此外,二氧化碳吸附热力学证实了物理化学协同吸附作用,Qst 降至 31-42 kJ/mol,并获得了良好的循环稳定性。综上所述,该多孔吸附剂具有良好的工业应用前景。© 2024 化学工业协会和 John Wiley & Sons, Ltd. 保留所有权利。
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