Mechanism of phosphate adsorption on superparamagnetic microparticles modified with transitional elements: Experimental observation and computational modelling

Microparticle sorbents (MPSs) containing nano-Fe3O4 core, nano-layered double hydroxides shell modified with different transitional elements (TE-MPSs) are effective for capturing phosphate from wastewater. In present article, different TE-MPSs loaded with Ce, La, Zr and Hf were synthesized and the p...

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Veröffentlicht in:Chemosphere (Oxford) 2020-11, Vol.258, p.127327-127327, Article 127327
Hauptverfasser: Zhao, Qian, Liu, Chengfang, Song, Hongquan, Liu, Yu, Wang, Hongbo, Tian, Fuyang, Meng, Shujun, Zhang, Kefeng, Wang, Ning, Mu, Ruimin, Li, Mei
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Sprache:eng
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Zusammenfassung:Microparticle sorbents (MPSs) containing nano-Fe3O4 core, nano-layered double hydroxides shell modified with different transitional elements (TE-MPSs) are effective for capturing phosphate from wastewater. In present article, different TE-MPSs loaded with Ce, La, Zr and Hf were synthesized and the phosphorous removal performances were compared. The molecular-level mechanism of phosphate adsorption was successfully simulated by pseudo-atom model based on virtual crystal approximation method, which was in line with the spectroscopic data. The results confirmed the inter-sphere complexation reaction between phosphate and TE-MPSs under neutral pH. And the adsorption mechanism probably changed during cycles of adsorption/regeneration. As revealed by elemental composition analysis, ion exchange mechanism probably played an important part in phosphate adsorption in Cycle 1 while the ligand complexation became dominant after regenerated with NaOH in the following cycles. This work indicates that the highly effective, easily separable and repeatedly usable TE-MPSs has the potential for phosphate sequestration and recovery from sewage wastewater. •EM-MPSs were developed to recovery phosphate from DSL and DSW.•Inner-sphere complexation was the dominant adsorption mechanism of P with TE-MPSs.•Ion exchange probably dominated in the P adsorption with TE-MPSs in Cycle 1.
ISSN:0045-6535
1879-1298
DOI:10.1016/j.chemosphere.2020.127327