沸石咪唑盐骨架
物理吸附
吸附
化学工程
咪唑酯
光催化
膜
化学
降级(电信)
挥发性有机化合物
甲苯
范德瓦尔斯力
金属有机骨架
布基纸
多孔性
无机化学
聚合物
水蒸气
X射线光电子能谱
材料科学
吸附
甲基蓝
朗缪尔
化学稳定性
地下水修复
光化学
作者
Vijayarohini Parasuraman,Yogesh Hari Krishnan,Woo Ram Lee,Syeda Mahnoor Zehra,Huyen Ngoc Ly,Su Jeong Sim,Tae Uk Han,Seungdo Kim
出处
期刊:Chemsuschem
[Wiley]
日期:2026-02-18
卷期号:19 (4): e202501998-e202501998
被引量:2
标识
DOI:10.1002/cssc.202501998
摘要
A major obstacle to the commercial application of metal‐organic frameworks (MOFs) is that their powder form hinders scalable membrane fabrication and significantly compromises stability under humid conditions. To address these limitations, this study presents a novel, humidity‐resistant zeolitic imidazolate framework ZIF‐67/alumina composite membrane (MMF) that combines visible‐light volatile organic compound (VOC) degradation and CO 2 adsorption in a single, scalable platform. Using an in situ self‐conversion strategy, ZIF‐67 crystals were directly anchored onto porous alumina, providing strong interfacial bonding, mechanical durability, and efficient mass transport. The MMF exhibited excellent toluene adsorption, as described by the Langmuir model, and achieved 96.4% photocatalytic degradation under visible light. Radical‐trapping and Electron spin resonance (ESR) studies confirmed superoxide anions ( . O 2 − ) as the dominant active species. The photocatalytic performance declined at 70–80% relative humidity (RH). To overcome this, ultrathin hydrophobic polysiloxane and perfluorinated polymer coatings minimized water uptake and maintained >92% photocatalytic activity, as supported by water vapor isotherms. Beyond VOC abatement, the MMFs demonstrated promising CO 2 adsorption predominantly by physisorption with higher uptake at low temperature and high pressure, attributed to enhanced pore filling and van der Waals interactions with nitrogen‐rich active sites. This work establishes a scalable strategy for MOF‐based membranes for simultaneous VOC abatement and CO 2 capture, offering a promising pathway for air‐purification technologies.
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