材料科学
复合数
吸附
铬
膜
纤维
氢键
复合材料
化学工程
氢
分子
冶金
有机化学
化学
生物
工程类
遗传学
作者
Juanjuan Li,Baohui Shi,Fei Gao,Hui Liu,Xuhan Zheng,Yan He,Qingyan Pan,Junqing Chen,Xueji Zhang,Lijun Qu,Chaoji Chen,Yingjie Zhao,Yuanyuan Shang
标识
DOI:10.1021/acsami.5c02896
摘要
Covalent organic frameworks (COFs) are widely used due to their high structural order, tunable pore size, and large specific surface area. However, COFs are typically bulk solid microcrystalline powders that are insoluble and challenging to process, which significantly impacts their application prospects. We report a method for the in situ growth of COF-COOH on the surface of polyacrylonitrile (PAN) fibers by using electrospinning. COFs were synthesized via a solvothermal method suitable for most COF materials. Nitrogen atoms in the nitrile groups of the PAN macromolecular chain form hydrogen bonds with the hydrogen atoms of the monomer 2,5-diamino-terephthalic acid (DABDA). This interaction facilitates the effective mixing of PAN and DABDA, resulting in the uniform growth of COF-COOH, which adheres firmly to the fiber surface. The resulting PAN@COF-COOH fiber membrane exhibits remarkable structural stability. It has obvious adsorbability to chromium(VI) (Cr(VI)) in aqueous solution under acidic conditions and also for cationic dyes such as Rhodamine B and methylene blue. It is revealed that COF materials exhibit selective adsorption due to pore size limitations. The integration of the electrospinning method with COF materials allows for the large-scale production of COF fiber membranes, which holds significant importance and offers broad application prospects in this field.
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