过硫酸盐
催化作用
降级(电信)
化学
吸附
2,4-二氯苯酚
机制(生物学)
金属
化学工程
环境化学
无机化学
有机化学
地质学
电信
古生物学
计算机科学
细菌
哲学
认识论
工程类
作者
Shuang Zhou,Yonglian Hu,Minglei Yang,Yun Liu,Qingke Li,Yanhong Wang,Guohua Gu,Min Gan
标识
DOI:10.1016/j.envres.2023.115639
摘要
Superabsorbent resin (SAR) saturated with heavy metals poses a threat to surrounding ecosystem. To promote the reutilization of waste, resins adsorbed by Fe2+ and Cu2+ were carbonized and used as catalysts ([email protected]/[email protected]) to activate persulfate (PS) for 2,4-dichlorophenol (2,4-DCP) degradation. The heterogeneous catalytic reaction was mainly responsible for 2,4-DCP removal. The synergistic effect of [email protected] and [email protected] was propitious to 2,4-DCP degradation. [email protected]/[email protected] with a ratio of 2:1 showed the highest performance of 2,4-DCP removal. 40 mg/L 2,4-DCP was completely removed within 90 min under reaction conditions of 5 mM PS, pH = 7.0 and T = 25 °C. The cooperation of [email protected] and [email protected] facilitated the redox cycling of Fe and Cu species to supply accessible PS activation sites, enhancing ROS generation for 2,4-DCP degradation. Carbon skeleton enhanced 2,4-DCP removal via radical/nonradical oxidation pathways and via its adsorption to 2,4-DCP. SO4˙ˉ, HO˙ and O2•− were the dominate radical species involved in 2,4-DCP destruction. Meanwhile, the possible pathways of 2,4-DCP degradation were proposed based on GC-MS. Finally, recycling tests proved catalysts exhibited recyclable stability. Aiming to resource utilization, [email protected]/[email protected] with satisfactory catalysis and stability, is promising catalyst for contaminated water treatment.
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