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用于高性能气体分离的“全聚酰亚胺”混合基质膜

"All Polyimide" Mixed Matrix Membranes for High Performance Gas Separation.

作者信息

Li Maijun, Zheng Zhibo, Zhang Zhiguang, Li Nanwen, Liu Siwei, Chi Zhenguo, Xu Jiarui, Zhang Yi

机构信息

PCFM Lab, GD HPPC Lab, Guangdong Engineering Technology Research Centre for High-performance Organic and Polymer Photoelectric Functional Films, State Key Laboratory of Optoelectronic Materials and Technologies, School of Chemistry, Sun Yat-sen University, Guangzhou 510275, China.

State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China.

出版信息

Polymers (Basel). 2021 Apr 19;13(8):1329. doi: 10.3390/polym13081329.

Abstract

To improve the interfacial compatibility of mixed matrix membranes (MMMs) for gas separation, microporous polyimide particle (AP) was designed, synthesized, and introduced into intrinsic microporous polyimide matrix (6FDA-Durene) to form "all polyimide" MMMs. The AP fillers showed the feature of thermal stability, similar density with polyimide matrix, high porosity, high fractional free volume, large microporous dimension, and interpenetrating network architecture. As expected, the excellent interfacial compatibility between 6FDA-Durene and AP without obvious agglomeration even at a high AP loading of 10 wt.% was observed. As a result, the CO permeability coefficient of MMM with AP loading as low as 5 wt.% reaches up to 1291.13 Barrer, which is 2.58 times that of the pristine 6FDA-Durene membrane without the significant sacrificing of ideal selectivity of CO/CH. The improvement of permeability properties is much better than that of the previously reported MMMs, where high filler content is required to achieve a high permeability increase but usually leads to significant agglomeration or phase separation of fillers. It is believed that the excellent interfacial compatibility between the PI fillers and the PI matrix induce the effective utilization of porosity and free volume of AP fillers during gas transport. Thus, a higher diffusion coefficient of MMMs has been observed than that of the pristine PI membrane. Furthermore, the rigid polyimide fillers also result in the excellent anti-plasticization ability for CO. The MMMs with a 10 wt.% AP loading shows a CO plasticization pressure of 300 psi.

摘要

为了提高用于气体分离的混合基质膜(MMMs)的界面相容性,设计、合成了微孔聚酰亚胺颗粒(AP),并将其引入固有微孔聚酰亚胺基质(6FDA-均苯四甲酸二酐)中以形成“全聚酰亚胺”MMMs。AP填料具有热稳定性、与聚酰亚胺基质相似的密度、高孔隙率、高自由体积分数、大微孔尺寸和互穿网络结构等特点。正如预期的那样,即使在10 wt.%的高AP负载量下,也观察到6FDA-均苯四甲酸二酐与AP之间具有优异的界面相容性,且无明显团聚现象。结果,AP负载量低至5 wt.%的MMM的CO渗透系数高达1291.13 Barrer,是原始6FDA-均苯四甲酸二酐膜的2.58倍,同时CO/CH的理想选择性没有显著牺牲。其渗透性能的改善比先前报道的MMMs要好得多,在先前的MMMs中,需要高填料含量才能实现高渗透性增加,但通常会导致填料的明显团聚或相分离。据信,PI填料与PI基质之间优异的界面相容性促使在气体传输过程中AP填料的孔隙率和自由体积得到有效利用。因此,观察到MMMs的扩散系数高于原始PI膜。此外,刚性聚酰亚胺填料还导致MMMs对CO具有优异的抗增塑能力。AP负载量为10 wt.%的MMMs的CO增塑压力为300 psi。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b0d/8073420/2b8fe1296bdd/polymers-13-01329-sch001.jpg

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