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

被引:5
|
作者
Mahata, Biplab K. [1 ,3 ]
Chang, Sue-Min [1 ,2 ]
Bose, Purnendu [3 ]
机构
[1] Natl Yang Ming Chiao Tung Univ, Int Coll Semicond Technol, 1001 Univ Rd, Hsinchu, Taiwan
[2] Natl Yang Ming Chiao Tung Univ, Inst Environm Engn, 1001 Univ Rd, Hsinchu 30010, Taiwan
[3] Indian Inst Technol, Dept Civil Engn, Kanpur 208016, UP, India
关键词
Hybrid anion exchanger; Complexation; Hydrogen bonds; Selectivity; Mechanism; WASTE-WATER; PHOSPHORUS REMOVAL; SELECTIVE REMOVAL; MASS-TRANSFER; RECOVERY; RESIN; EUTROPHICATION; SPECIFICITY; KINETICS; COMPLEX;
D O I
10.1016/j.seppur.2022.121339
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
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 Cu2+ 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 Cu2+ ions mainly drove phosphate diffusion from the liquid to the resin and then induced the phosphate species to bond with multiple -NH2-/-NH groups. Such adsorption exhibited a high entropy (Delta S-0 = 132.47 J/mol-K) and was highly exergonic (Delta G(0) = -16.83 similar to -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 Cu2+ -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.
引用
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页数:13
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