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Controlled Superacid-Catalyzed Self-Cross-Linked Polymer of Intrinsic Microporosity for High-Performance CO2 Separation
Macromolecules ( IF 5.1 ) Pub Date : 2020-08-31 , DOI: 10.1021/acs.macromol.0c01590 Shengyang Zhou 1, 2 , Yuxuan Sun 1, 2 , Boxin Xue 1, 2 , Shenghai Li 1, 2 , Jifu Zheng 1, 2 , Suobo Zhang 1, 2
Macromolecules ( IF 5.1 ) Pub Date : 2020-08-31 , DOI: 10.1021/acs.macromol.0c01590 Shengyang Zhou 1, 2 , Yuxuan Sun 1, 2 , Boxin Xue 1, 2 , Shenghai Li 1, 2 , Jifu Zheng 1, 2 , Suobo Zhang 1, 2
Affiliation
Polymers of intrinsic microporosity (PIMs) with superhigh permeability have been widely studied for higher selectivity in the various separation processes. However, the disorder and wide-distribution of pore size limit their molecule selectivity. In this work, at low temperature (60 °C), we design and prepare a superacid-induced self-cross-linked PIM-1 membrane with a rebuilt microstructure by swelling and catalysis of the superacid to achieve fast and accurate gas transport. For PIM-1 membranes, the polymer chains can be activated by CF3SO3H solvation to possess enhanced motion and reactivity. Then, the partial swelled porosities can be solidified with cross-linking of nitrile groups and further be interconnected by narrow channels to form alternating gas pathways, which was supported by X-ray diffraction and small-angle X-ray scattering. As a result, these cross-linked membranes maintain high gas permeability, even approaching to that of pristine PIM-1, and meanwhile exhibit excellent molecular sieving ability, such as CO2/N2 permeation selectivity increasing from 20.4 to 58.1. This indicates that superacid-catalyzed self-cross-linking can effectively adjust the topological structure of PIM-1 for microstructure-dependent applications including but not limited to CO2 separation and fuel cells.
中文翻译:
可控超强酸催化固有性质的微孔自交联聚合物,用于高效CO 2分离
具有超高渗透性的本征微孔性(PIM)聚合物已被广泛研究以在各种分离过程中提高选择性。然而,孔径的无序和广泛分布限制了它们的分子选择性。在这项工作中,我们在低温(60°C)下设计并制备了一种由超酸诱导的自交联PIM-1膜,该膜通过溶胀和催化超酸来重建微观结构,从而实现了快速,准确的气体传输。对于PIM-1膜,聚合物链可以被CF 3 SO 3活化H溶剂化具有增强的运动性和反应性。然后,可以通过腈基的交联来固化部分溶胀的孔隙,并进一步通过狭窄的通道相互连接,形成交替的气体通道,这由X射线衍射和小角度X射线散射来支持。结果,这些交联的膜保持高的气体渗透性,甚至接近原始的PIM-1的气体渗透性,同时表现出优异的分子筛分能力,例如CO 2 / N 2的渗透选择性从20.4增加到58.1。这表明超酸催化的自交联可以有效地调节PIM-1的拓扑结构,以用于依赖于微结构的应用,包括但不限于CO 2分离和燃料电池。
更新日期:2020-09-22
中文翻译:
可控超强酸催化固有性质的微孔自交联聚合物,用于高效CO 2分离
具有超高渗透性的本征微孔性(PIM)聚合物已被广泛研究以在各种分离过程中提高选择性。然而,孔径的无序和广泛分布限制了它们的分子选择性。在这项工作中,我们在低温(60°C)下设计并制备了一种由超酸诱导的自交联PIM-1膜,该膜通过溶胀和催化超酸来重建微观结构,从而实现了快速,准确的气体传输。对于PIM-1膜,聚合物链可以被CF 3 SO 3活化H溶剂化具有增强的运动性和反应性。然后,可以通过腈基的交联来固化部分溶胀的孔隙,并进一步通过狭窄的通道相互连接,形成交替的气体通道,这由X射线衍射和小角度X射线散射来支持。结果,这些交联的膜保持高的气体渗透性,甚至接近原始的PIM-1的气体渗透性,同时表现出优异的分子筛分能力,例如CO 2 / N 2的渗透选择性从20.4增加到58.1。这表明超酸催化的自交联可以有效地调节PIM-1的拓扑结构,以用于依赖于微结构的应用,包括但不限于CO 2分离和燃料电池。