过硫酸盐
化学
吸附
双酚A
石墨烯
催化作用
无机化学
氧化物
反应速率常数
激进的
化学工程
协同催化
苯酚
核化学
有机化学
动力学
物理
量子力学
环氧树脂
工程类
作者
Xiaobo Wang,Yanlei Qin,Li Zhu,Heqing Tang
标识
DOI:10.1021/acs.est.5b01059
摘要
Nitrogen modified reduced graphene oxide (N-RGO) was prepared by a hydrothermal method. The nitrogen modification enhanced its adsorption and catalysis ability. For an initial bisphenol concentration of 0.385 mmol L–1, the adsorption capacity of N-RGO was evaluated as 1.56 and 1.43 mmol g–1 for bisphenol A (BPA) and 1.43 mmol g–1 for bisphenol F (BPF), respectively, both of which were about 1.75 times that (0.90 and 0.84 mmol g–1) on N-free RGO. N-RGO could activate persulfate, producing strong oxidizing sulfate radicals. The apparent degradation rate constant of BPA on N-RGO was 0.71 min–1, being about 700 times that (0.001 min–1) on N-free RGO. In mixtures of various phenols, the degradation rate constant of each phenol was linearly increased with its adsorption capacity. A simultaneous use of N-RGO and persulfate yielded fast and efficient removal of bisphenols. The use of N-RGO (120 mg L–1) and persulfate (0.6 mmol L–1) almost completely removed the added bisphenols (0.385 mmol L–1) at pH 6.6 within 17 min. A mechanism study indicated that the adsorption enriched the pollutant, and the catalytically generated sulfate radicals rapidly degrade the adsorbed pollutant, accelerating in turn the adsorption of residual pollutant.
科研通智能强力驱动
Strongly Powered by AbleSci AI