吸附
废水
吸附
化学
镍
化学工程
核化学
色散(光学)
动力学
环境工程
有机化学
量子力学
光学
物理
工程类
作者
Chenghan Ji,Jingyue Zhang,Ruxue Jia,Weiming Zhang,Lu Lv,Bingcai Pan
标识
DOI:10.1016/j.cej.2021.128812
摘要
Effective removal of toxic metal Ni(II) from wastewater is essential to water safety and human health. Although zeolitic imidazolate framework-8 (ZIF-8) has demonstrated outstanding selective removal of Ni(II) in high-salinity wastewater, the practical applications of ZIF-8 are mainly limited by low active sites utilization, slow adsorption kinetics and poor reusability. In this study, we prepared a novel negatively charged poly (sodium 4-styrenesulfonate) (PSS)-modified ZIF-8 adsorbent, [email protected] (12 h), which increased the adsorption rate of Ni(II) (kinetic constant k = 0.0299 g mg−1 min−1) by nearly 10 times and the adsorption capacity (329.58 mg/g) by 1.6 times compared to pristine ZIF-8 (k = 0.0021 g mg−1 min−1). [email protected] (12 h) (0.5 g/L) could quickly decrease Ni(II) (C0 = 1.0 mg/L) to 0.1 mg/L (discharged standard) in 25 min, while 600 min for ZIF-8. Batch experiments and characterization analyses revealed PSS can improve particle dispersion, increase active sites utilization, and strengthen Ni(II) diffusion kinetics, thereby enhancing the adsorption of Ni(II). Among them, the increase in active sites utilization of ZIF-8 contributes 83.3% to capacity improvement, while the –SO3− on PSS is 16.7%. Furthermore, the enhancements of adsorption kinetics and capacity were also applicable to other heavy metals (e.g., Cu2+, Pb2+, Cr3+, Cd2+). Column experiments using real nickel plating effluent shown that 1 g [email protected] (12 h) could produce ~3675 mL of clean water before breakthrough (Ni2+ < 0.1 mg/L). Moreover, a specific nickel chelator, dimethylglyoxime was used to regenerate the exhausted adsorbent and showed an insignificant capacity loss after four cycles. This study indicates the potential of [email protected] (12 h) to remove Ni(II) from nickel plating effluent.
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