Chitosan magnetic graphene grafted polyaniline doped with cobalt oxide for removal of Arsenic(V) from water

吸附 弗伦德利希方程 聚苯胺 物理吸附 石墨烯 化学吸附 朗缪尔吸附模型 化学工程 朗缪尔 材料科学 水溶液 核化学 氧化物 吉布斯自由能 吸热过程 化学 无机化学 聚合物 物理化学 纳米技术 有机化学 聚合 热力学 工程类 物理
作者
Mohammad Ali Gabris,Shahabaldin Rezania,Mahdi Rafieizonooz,Elnaz Khankhaje,Sandhanasamy Devanesan,Mohamad S. AlSalhi,Mamduh J. Aljaafreh,Arvin Shadravan
出处
期刊:Environmental Research [Elsevier]
卷期号:207: 112209-112209 被引量:44
标识
DOI:10.1016/j.envres.2021.112209
摘要

The present study reports the successful functionalization/magnetization of bio-polymer to produce chitosan-magnetic graphene oxide grafted polyaniline doped with cobalt oxide (ChMGOP-Co3O4). Analytical techniques furrier transform infra-red (FT-IR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) were used to confirm the formation of ChMGOP-Co3O4. The effects of several experimental factors (solution pH, adsorbent dosage and coexisting ions) on the uptake of As(V) ions using ChMGOP-Co3O4 were examined through batch experiments. As(V) removal process was validated by experimentally and theoretically investigating the adsorption capacity, rate, and thermal effects. Thermodynamic parameters such as free energy (ΔG°), entropy (ΔS°) and enthalpy (ΔH°) were also calculated and were used to explain the mechanism of adsorption. Based on the results, the sorbent showed a high adsorption capacities (90.91 mg/g) at favorable neutral pH and superior removal efficiencies as high as 89% within 50 min. In addition, the adsorption isotherm followed the Langmuir isotherm in compare to the Freundlich, due to its higher R2 value (0.992 < 0.941). Meanwhile, the kinetic data revealed that the of As(V) adsorption was controlled by pseudo-second-order. Overall, the adsorption mechanism studies revealed a spontaneous endothermic nature with predominance of physisorption over chemisorption. This study indicated that ChMGOP-Co3O4 is an exceptional novel adsorbent material for the efficient isolation of As(V) from aqueous media.
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