Phosphorus recovery from wastewater using extracellular polymeric substances (EPS)-like hydrogels

自愈水凝胶 吸附 化学 浸出(土壤学) 胞外聚合物 核化学 废水 腐植酸 氯化物 磷酸盐 动力学 有机化学 环境工程 土壤水分 环境科学 肥料 细菌 遗传学 土壤科学 生物膜 量子力学 工程类 物理 生物
作者
Xiao Tan,Lan Yi,Zhipeng Duan,Xiaoge Wu,Imran Ali,Li Gao
出处
期刊:Journal of water process engineering [Elsevier BV]
卷期号:52: 103512-103512
标识
DOI:10.1016/j.jwpe.2023.103512
摘要

Phosphorus (P) recovery from wastewater is meaningful in wastewater treatment and resource recycling. Natural extracellular polymeric substances (EPS) of microbes show impressive P uptake ability. However, natural EPS is difficult to assist in P recovery due to the high harvesting cost in extraction. Thus, EPS-like hydrogels constructed by sodium alginate (SA)-Fe(III) and humic acids(HA) were designed. The results showed that the optimal formation conditions of EPS-like hydrogel were 0.1 M Fe(III) and m(HA):m(SA) = 1. Fe(III) ions were the key crosslinkers in constructing the 3-dimensional sodium alginate (SA)-Fe(III) hydrogels and in the embedding of humic acid (HA) for [email protected](III) hydrogels. [email protected](III) hydrogels showed bigger pore sizes, lesser Fe leaching, and higher phosphate selectivity in SO42− compared to SA-Fe(III) hydrogels. The highest P adsorption amounts were 56 and 134.33 mg-P/g for the [email protected](III) and SA-Fe(III), respectively. The adsorption isotherm results exhibited that when the initial P concentration was in a range of 0–35 mg/L, the adsorption mainly existed on the surface of the adsorbent. While in the pore-filling stage (i.e., the initial P concentration was higher than 35 mg/L), internal diffusion controlled the adsorption process based on the kinetics. The X-ray photoelectron spectroscopy (XPS) analysis detected an appearance of Fe-O-P and O-P bonds and a disappearance of chloride ions in the hydrogels after adsorption, which confirmed the major driving forces on adsorption (ligand exchange and ion exchange). Moreover, [email protected](III) hydrogel saturated by P adsorption passed a test as sustainable-release P fertilizers. Overall, the EPS-like hydrogels developed here provide new absorbents for P recovery.

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