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首页> 外文期刊>Journal of Colloid and Interface Science >Microporous polyimides with high surface area and CO2 selectivity fabricated from cross-linkable linear polyimides
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Microporous polyimides with high surface area and CO2 selectivity fabricated from cross-linkable linear polyimides

机译:具有高表面积和来自可交联线性聚酰亚胺的高表面积和CO 2选择性的微孔聚酰亚胺

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Linear polyimides of intrinsic microporosity have been intensively investigated for gas separation due to their microporous structure and high surface area. The microporous structure in the linear polyimides of intrinsic microporosity comes from their contorted structure. Therefore, most linear polyimides without contorted structure do not have micropores. In this work, the microporous polyimides are constructed through the condensation of a cross-linkable dianhydride monomer with two novel nitrogen-rich diamine monomers and post crosslinking reaction. The linear polyimide precursors without contorted structure have the same main-chain structure. The introduction of crosslinked structure endow the crosslinked polyimides (PI-CLs) with microporous structure. The microporous structure in PI-CLs can be tuned by changing the substituents of the linear polyimide precursors. The PI-CLs have competitive CO2 uptake capacity (7.3-9.4 wt%) at 273 K and 1 bar. Particularly, the crosslinked polyimide containing trifluoromethyl groups (CF3 -PI-CL) shows high CO2/N-2 and CO2/CH4 selectivity (72 and 22) at 273 K, which are among the best results for reported porous materials. This work reveals that the introduction of crosslinked structure and changing substituents is an efficient method for constructing microporous polyimides with abundant micropores and excellent CO2 selective adsorption capacity. This method also has great potential for fabricating high-performance microporous polymers based on other linear poly- mers without rigid contorted structure. (C) 2020 Elsevier Inc. All rights reserved.
机译:由于其微孔结构和高表面积,已经强烈地研究了固有微孔的线性聚酰亚胺。内在微孔的线性聚酰亚胺中的微孔结构来自其扭曲的结构。因此,没有扭曲结构的大多数线性聚酰亚胺没有微孔。在这项工作中,微孔聚酰亚胺通过具有两种新的富含氮二胺单体和后交联反应的可交联二酐单体的冷凝构成。没有扭曲结构的线性聚酰亚胺前体具有相同的主链结构。交联结构的引入赋予了微孔结构的交联的聚酰亚胺(PI-CLS)。通过改变线性聚酰亚胺前体的取代基可以调节PI-CLS中的微孔结构。 PI-CLS在273 k和1巴的竞争性二氧化碳吸收能力(7.3-9.4wt%)。特别地,含有三氟甲基(CF3-PI-CL)的交联聚酰亚胺在273k处显示出高CO 2 / N-2和CO 2 / CH 4选择性(72和22),这是报告多孔材料的最佳结果。本作作品揭示了交联结构和变化取代基的引入是构建具有丰富微孔的微孔聚酰亚胺的有效方法和优异的CO 2选择性吸附能力。该方法还具有基于没有刚性扭曲结构的其他线性聚酯来制造高性能微孔聚合物的潜力。 (c)2020 Elsevier Inc.保留所有权利。

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