Preferable phosphate sequestration using polymer-supported Mg/Al layered double hydroxide nanosheets

吸附 层状双氢氧化物 氢氧化物 磷酸盐 化学 氧阴离子 无机化学 膨润土 化学工程 朗缪尔 浸出(土壤学) 有机化学 催化作用 土壤水分 土壤科学 工程类 环境科学
作者
Guangze Nie,Lirui Wu,Shijun Qiu,Zhengwen Xu,Hai‐Ling Wang
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:614: 583-592 被引量:43
标识
DOI:10.1016/j.jcis.2022.01.158
摘要

The efficient removal of phosphate from waters is critical to mitigating eutrophication. Recently, layered double hydroxides (LDHs) have been believed to be promising adsorbents for phosphate removal. Nevertheless, the scaled-up application of LDHs is limited by the difficulties of separation, excessive pressure drops, and potential metal leaching. In this study, a millimeter-sized nanocomposite, MgAl-201, was fabricated by impregnating Mg/Al LDH nanosheets into a polystyrene anion exchanger D201. The resulting MgAl-201 combines the inherent affinity of Mg/Al LDH toward phosphate and the excellent hydrodynamic performance of the support material. Benefiting from the shielding effect from the cross-linked polymeric host, MgAl-201 exhibits satisfactory chemical stability in the range of pH 3-11 with a negligible metal release. Adsorption experiments show that MgAl-201 has superb applicability to neutral phosphate-contaminated waters. It reaches adsorption equilibrium within 270 min, and the maximum adsorption capacity calculated by the double Langmuir model is 52.0 mg/g. Meanwhile, MgAl-201 exhibits more preferable adsorption toward phosphate than D201 when coexisting anions are at relatively high levels. FTIR and XPS surveys revealed that two distinct adsorption interactions were involved in phosphate removal, that is, electrostatic interactions from the quaternary ammonium groups bonded on the host and the interlayer exchangeable anions in the encapsulated Mg/Al LDH, and specific inner-sphere complexation from the -OH groups in the Mg/Al LDH layers. For wastewater application, a satisfactory treatable volume of 580 BV was achieved to reduce the effluents from 2.0 mg/L to 0.5 mg/L, which was up to 8 times that of the traditional anion exchanger D201. Furthermore, MgAl-201 could be easily regenerated using the Na2CO3-NaCl binary solution and maintained good reusability without significant capacity loss after 5 adsorption-desorption cycles. The results suggest that MgAl-201 is of great application capability for preferable phosphate sequestration in advanced wastewater treatment.
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