吸附
砷
原位
化学
壳聚糖
化学工程
无机化学
材料科学
环境化学
有机化学
物理化学
工程类
作者
Jessy Joseph,Ari Väisänen,Ajay B. Patil,Manu Lahtinen
标识
DOI:10.1016/j.jhazmat.2023.132893
摘要
Efficient sequestration of arsenic from drinking water is a global need. Herein we report eco-friendly porous hybrid adsorbent beads for removal of arsenic, through in situ synthesis of MIL-100(Fe) in the chitosan solvogel. To understand the structural vs. performance correlation, series of hybrid adsorbents were synthesized by modulating synthesis conditions like temperature, crystallization time, and concentration. Adsorbents were investigated using PXRD, FT-IR, SEM, and ICP-OES. Intriguing correlation between crystallinity and adsorption performance was observed as low and high crystalline MIL-100(Fe)-chitosan (ChitFe5 and ChitFe7, respectively) exhibited exceptional adsorption towards As5+ by removing it from water with 99% efficiency, whereas for As3+ species removal of about 85% was afforded. Adsorption isotherms indicated that increase in crystallinity (ChitFe5 -> ChitFe7), adsorption capacities of As5+ and As3+ increased from 23.2 to 64.5, and from 28.1 to 35.3 mg/g, respectively. Selectivity tests of the adsorbents towards As5+ and As3+ over competitive anions in the equimolar competitive systems having nitrates, sulfates, and carbonates demonstrated that the performance of the absorbents was fully maintained, relative to the control system. Through this study a highly selective and efficient adsorbent for arsenic species is designed and a clear insight into the structural tuning and its effect on adsorption performance is provided. Arsenic is one of the elements with a threatening effect on human health from prolonged exposure even at acute concentrations. The major issue of concern with arsenic is that the prominent carrier of this deadly pollutant to the human body is drinking water. Developing countries like Bangladesh, India, and Ghana are the areas most affected by arsenic poisoning. Through this study, we design a new adsorbent with a high selectivity and adsorption capacity to mitigate arsenic content from aqueous systems. Moreover, we aimed to create a clear insight regarding to the effects of the structural alterations for the adsorption capacity of the adsorbent.
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