吸附
甲基丙烯酸缩水甘油酯
螯合作用
化学
嫁接
离子交换
X射线光电子能谱
胺气处理
核化学
朗缪尔吸附模型
聚丙烯
质子化
动力学
无机化学
高分子化学
化学工程
有机化学
离子
单体
聚合物
物理
量子力学
工程类
作者
Xiaohan Pan,Lingxiao Fu,Huan Wang,Yi Xue,Jianhua Zu
标识
DOI:10.1016/j.seppur.2021.118778
摘要
• A novel sulfydryl-functionalized chelating adsorbent is synthesized by radiation grafting using stable polypropylene non-woven fabrics. • The adsorbent contains two functional groups, amine and sulfhydryl. • The adsorbent has two adsorption mechanisms for silver(Ⅰ) under high acid: ion exchange and chelate adsorption. The sulfhydryl has an excellent chelating affinity towards silver(Ⅰ) and the protonated amine adsorbs [Ag(NO 3 ) 2 ] −1 by ion exchange. • Silver(Ⅰ) is effectively and selectively adsorbed in high acid environment. A novel sulfydryl-functionalized adsorbent PP-g-GMA@MEA for recovery of Ag(I) was synthesized by γ-ray induced simultaneous grafting of glycidyl methacrylate (GMA) onto polypropylene (PP) non-woven fabric, followed by ring-opening processes with mercaptoethylamine (MEA). The obtained adsorbents before and after adsorption of Ag(I) were fully characterized by SEM, EDS, FT-IR spectra, XRD and XPS. Batch adsorption experiments were carried out to evaluate adsorption abilities of the adsorbents under high acidity. The adsorption kinetics of Ag(I) were well fitted with pseudo-second-order kinetics model. The maximum adsorption capacity calculated by the Langmuir isotherm model was 262.51 mg/g at 25 °C. EDS, XRD and XPS analyses confirmed the mechanism of adsorption under high acidity was chelating reaction between -SH and Ag(I) and ion exchange adsorption towards [Ag(NO 3 ) 2 ] −1 . Through competitive adsorption tests, the PP-g-GMA@MEA was found remarkably selective towards Ag(I) when it coexisted with Cu(II), Co(II), Ni(II) and Cr(III) in high acidity medium. Therefore, the developed PP-g-GMA@MEA composite would be a promising adsorbent for Ag(I) recovery from industrial effluents.
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