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
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
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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