首页|Bio-Inspired phosphate adsorption by Copper-Decorated weak base anion exchanger

Bio-Inspired phosphate adsorption by Copper-Decorated weak base anion exchanger

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Hybrid-based phosphate adsorbents have high adsorption ability but are challenged with regeneration because of strong bonding.Inspired by phosphate-binding proteins(PBPs)which reached a trade-off between high adsorption and regeneration ability by binding phosphate species with multiple hydrogen bonds,a weak-base anion(WBA)exchange resin was decorated with Cu~(2+)ions to develop an alternative advanced phosphate adsorbent.Different from the role of metal species in the promoted adsorption of existing hybrid-based adsorbents,the Cu~(2+)ions mainly drove phosphate diffusion from the liquid to the resin and then induced the phosphate species to bond with multiple-NH_2~+/-NH groups.Such adsorption exhibited a high entropy(AS0 = 132.47 J/mol-K)and was highly exergonic(ΔG~0 =-16.83 ~-20.14 kJ/mol).Moreover,it enhanced the phosphate selectivity because the driving force for the sorption process originated from the complexation.During the regeneration,the Cu~(2+)-to-Cu-O~-transformation could occur under weak alkaline conditions and repelled the adsorbed phosphate species to facilitate desorption.Therefore,the Cu-WBA resin not only exhibited high phosphate adsorptions(31.94 to 61.03 mg-P/g)and high competing-anion tolerance but also was successfully recovered with a diluted NaOH solution(0.05 N).Detailed adsorption behaviors under different pHs,temperatures,and interference of competing anions were examined,and the mechanisms were elucidated.

Hybrid anion exchangerComplexationHydrogen bondsSelectivityMechanism

Biplab K.Mahata、Sue-min Chang、Purnendu Bose

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International College of Semiconductor Technology,National Yang Ming Chiao Tung University,1001 University Road,Hsinchu,Taiwan

Department of Civil Engineering,Indian Institute of Technology,Kanpur,UP 208016,India

2022

Separation and Purification Technology

Separation and Purification Technology

EISCI
ISSN:1383-5866
年,卷(期):2022.296
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