零价铁
化学
降级(电信)
废水
可重用性
羟基自由基
核化学
硫酸盐
芬顿反应
超声
光催化
催化作用
生物降解
高级氧化法
激进的
环境化学
化学工程
色谱法
有机化学
环境工程
吸附
环境科学
电信
软件
计算机科学
程序设计语言
作者
Gelavizh Barzegar,Helder Gomes,Vahid Zarezade,Masoumeh Khatebasreh,Fayyaz Mehdipour,Farshid Ghanbari
出处
期刊:Chemosphere
[Elsevier BV]
日期:2018-06-01
卷期号:201: 370-379
被引量:134
标识
DOI:10.1016/j.chemosphere.2018.02.143
摘要
In this study, nanoscale-zero valent iron (nZVI) was synthesized and its function was assessed in ultrasound (US)/peroxymonosulfate (PMS)/nZVI process to degrade 4-chlorphenol (4-CP). The influential operation parameters of US/PMS/nZVI were evaluated on 4-CP degradation. 95% of 4-CP was degraded during 30 min under the conditions of pH = 3.0, nZVI = 0.4 g/L, PMS = 1.25 mM, US power = 200 W. The rate constants of 4-CP degradation for US/PMS/nZVI, PMS/nZVI, US/PMS and US/nZVI were 0.1159, 0.03, 0.0134 and 0.0088 min-1 respectively. Simultaneous application of US and nZVI synergistically increased 4-CP degradation and PMS activation. nZVI was compared with Fe2+, Fe3+ and micro-ZVI and their results indicated high performance of nZVI compared to others. Reusability of nZVI was examined in four cycles. nZVI exhibited that reusability was acceptable in three runs. The results of effect of anions showed that phosphate had significant inhibitory effect on 4-CP degradation in US/PMS/nZVI process. The scavenging experiments indicated that hydroxyl radical had more contribution compared to sulfate radical. Intermediates of 4-CP degradation were identified including five aromatic compounds. Reaction pathway of 4-CP degradation was proposed. Finally, the performance of US/PMS/nZVI process was evaluated on real petrochemical wastewater. The results showed that US/PMS/nZVI can be a suitable pretreatment for biological treatment.
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