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使用功能化TiCT大幅提高Matrimid的CO渗透性和CO/CH选择性。

Substantially Improving CO Permeability and CO/CH Selectivity of Matrimid Using Functionalized-TiCT.

作者信息

Mozafari Mohammad, Khoshhal Salestan Saeed, Arabi Shamsabadi Ahmad, Jha Kritika, Tanwar Manushree, Kim Hyehyun, Fakhraai Zahra, Soroush Masoud

机构信息

Department of Chemical and Biological Engineering, Drexel University, Philadelphia, Pennsylvania 19104, United States.

Department of Chemical Engineering, Babol Noshirvani University of Technology, Babol 47148-71167, Iran.

出版信息

ACS Appl Mater Interfaces. 2025 Jan 15;17(2):3897-3910. doi: 10.1021/acsami.4c17315. Epub 2025 Jan 2.

Abstract

Mixed-matrix membranes (MMMs) with favorable interfacial interactions between dispersed and continuous phases offer a promising approach to overcome the traditional trade-off between permeability and selectivity in membrane-based gas separation. In this study, we developed free-standing MMMs by embedding pristine and surface-modified TiCT MXenes into Matrimid 5218 polymer for efficient CO/CH separation. Two-dimensional TiCT with adjustable surface terminations provided control over these critical interfacial interactions. Characterization (Raman spectroscopy, XPS, DSC, FTIR) indicated the formation of hydrogen bonds between the termination groups on TiCT and the carbonyl groups of Matrimid, promoting enhanced compatibility and dispersion of MXenes within the polymer matrix. The resulting MMMs with 5 wt % TiCT showed a 67% increase in CO permeability and an 84% enhancement in CO/CH selectivity compared to pristine Matrimid membranes. Surface modification of TiCT using [3-(2-aminoethylamino)propyl]trimethoxysilane (AEAPTMS) further enhanced compatibility, leading to MMMs with 140% higher CO permeability and 130% greater CO/CH selectivity. Molecular simulations suggested that AEAPTMS functionalization improved interfacial interactions with Matrimid chains, increasing the affinity of MXenes toward CO molecules. Additionally, the elongation of gas pathways, polymer chain disruption, and the presence of interlayer nanogalleries contributed positively to the enhanced separation performance. This work provides insights into tailoring nanomaterial-polymer interfaces to address the challenges of gas separation, paving the way for environmentally friendly CO separation technologies.

摘要

在分散相和连续相之间具有良好界面相互作用的混合基质膜(MMM)为克服基于膜的气体分离中渗透率和选择性之间的传统权衡提供了一种很有前景的方法。在本研究中,我们通过将原始的和表面改性的TiCT MXene嵌入Matrimid 5218聚合物中来制备独立的MMM,以实现高效的CO/CH分离。具有可调节表面端基的二维TiCT能够控制这些关键的界面相互作用。表征(拉曼光谱、X射线光电子能谱、差示扫描量热法、傅里叶变换红外光谱)表明,TiCT上的端基与Matrimid的羰基之间形成了氢键,促进了MXene在聚合物基质中的相容性和分散性增强。与原始的Matrimid膜相比,含有5 wt% TiCT的所得MMM的CO渗透率提高了67%,CO/CH选择性提高了84%。使用[3-(2-氨基乙氨基)丙基]三甲氧基硅烷(AEAPTMS)对TiCT进行表面改性进一步增强了相容性,得到的MMM的CO渗透率提高了140%,CO/CH选择性提高了130%。分子模拟表明,AEAPTMS功能化改善了与Matrimid链的界面相互作用,增加了MXene对CO分子的亲和力。此外,气体通道的延长、聚合物链的破坏以及层间纳米画廊的存在对分离性能的提高有积极贡献。这项工作为定制纳米材料-聚合物界面以应对气体分离挑战提供了见解,为环境友好型CO分离技术铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14f2/11744502/5881cf6716b1/am4c17315_0001.jpg

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