光催化
双酚A
吸附
降级(电信)
辐照
X射线光电子能谱
复合数
化学工程
可见光谱
激进的
光化学
核化学
反应速率常数
朗缪尔吸附模型
材料科学
化学
动力学
复合材料
催化作用
光电子学
有机化学
环氧树脂
计算机科学
电信
物理
工程类
量子力学
核物理学
作者
Hongjie Zhu,Zhengkui Li,Jianhua Yang
标识
DOI:10.1016/j.cej.2017.11.148
摘要
A novel hydrogel catalyst (P(HEA-co-HAM)-CdS) was synthesized to remove bisphenol A (BPA) from water through adsorption and in-situ photocatalytic degradation. The characterization of P(HEA-co-HAM)-CdS hydrogel through SEM-EDS, TEM, XPS and FT-IR demonstrated heterogeneous structure and chemical combination between CdS and hydrogel. Besides, the optical properties of P(HEA-co-HAM)-CdS hydrogel illustrated enhanced photocatalytic activity under visible light irradiation with efficient separation ability of electron-hole pairs and effective visible light utilization capability. In addition, the ability of hydrogel in adsorption and degradation were observed. BPA adsorption capacity of P(HEA-co-HAM)-CdS hydrogel was 11.26 mg/g, higher than similar adsorbents. The adsorption process fitted in pseudo-second-order rate equation and Langmuir monolayer adsorption. Under 500 W visible light irradiation, BPA degradation rate of P(HEA-co-HAM)-CdS hydrogel reached 92% in 3 h and photocatalytic oxidative radicals detection experiment verified holes (h+) and ·O2− play major role in this system, mineralization rate of BPA was 47%. HPLC-TOF-MS was employed to detect the degradation intermediates, with theoretically Fed2 value calculating results, possible degradation pathway of BPA was proposed. Furthermore, degradation rate remained over 84.4% after recycle. The results indicated that P(HEA-co-HAM)-CdS hydrogel was a promising catalyst material in application.
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