4.7 Article

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

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 614, Issue -, Pages 583-592

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.01.158

Keywords

Phosphate removal; Polymeric nanocomposite; Layered double hydroxides; Selective adsorption

Funding

  1. National Key R&D Program of China [2017YFE0107200]
  2. National Natural Science Foundation of China [21507060, 22176096]
  3. Postgraduate Research & Practice Innovation Program of Jiangsu Province [SJCX21_0460]

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Efficient removal of phosphate is crucial for addressing eutrophication. A millimeter-sized nanocomposite, MgAl-201, was developed by impregnating Mg/Al LDH nanosheets into a polystyrene anion exchanger. MgAl-201 exhibited excellent adsorption performance and chemical stability in a wide pH range. It showed great potential for phosphate removal from neutral contaminated waters and achieved a treatable volume 8 times that of traditional anion exchangers.
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 innersphere 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.(c) 2022 Elsevier Inc. All rights reserved.

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