Efficient adsorption removal of anionic dyes by an imidazolium-based mesoporous poly(ionic liquid) including the continuous column adsorption-desorption process

吸附 化学 解吸 介孔材料 离子液体 弗伦德利希方程 无机化学 朗缪尔 氯化物 有机化学 催化作用
作者
Ju Lin,Tiezhu Su,Jiawen Chen,Tianwei Xue,Shuliang Yang,Peiwen Guo,Hongying Lin,Hongtao Wang,Yanzhen Hong,Yuzhong Su,Peng Li,Jun Li
出处
期刊:Chemosphere [Elsevier BV]
卷期号:272: 129640-129640 被引量:70
标识
DOI:10.1016/j.chemosphere.2021.129640
摘要

The mesoporous poly(N,N′-methylene-bis(1-(3-vinylimidazolium)) chloride), labeled as PDVIm-Cl, with double anions (Cl−) and low monomer molecular weight was synthesized and applied in the adsorption of anionic dyes (acid orange 7 (AO7), sunset yellow (SY), reactive blue 19 (RB19), congo red (CR)). Due to the mesoporous structure, abundant Cl− and positively charged imidazole rings, the poly(ionic liquid) (PIL) exhibited superior adsorption ability towards anionic dyes. What is more, the RB19 adsorption by PDVIm-Cl could achieve the highest capacity (2605 ± 254 mg g−1) which was nearly twice higher than the maximum adsorption capacity of the previously reported materials. All the adsorption kinetic data and isotherms fitted well with the pseudo second-order model and Langmuir-Freundlich model. To better explore the practical potential of the PIL for dye adsorption, the adsorption under different pH values and column adsorption performances were also evaluated. Results showed that PDVIm-Cl exhibited high removal efficiencies for anionic dyes over a wide pH range (2−10). Also, the great reusability could be well demonstrated by the achievable continuous column adsorption-desorption process. It is worth mentioning that the regeneration could be realized with very little desorbent which was far less than the adsorption volume flowing through the column and the desorption efficiency was well maintained after three consecutive cycles. At last, the adsorption mechanism was explored by experiments combined with quantum chemical calculations and showed anionic dyes adsorption by PDVIm-Cl was a joint process dominated by the ion exchange, electrostatic interaction, hydrogen bond and π-π stacking.
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