Activation of sodium percarbonate with ferrous ions for degradation of chlorobenzene in aqueous solution: mechanism, pathway and comparison with hydrogen peroxide

氯苯 化学 过氧化氢 水溶液 无机化学 降级(电信) 铁质 激进的 电子顺磁共振 核化学 催化作用 有机化学 计算机科学 电信 物理 核磁共振
作者
Sai Zhang,Xuebin Hu,Li Li,Xiaoliu Huangfu,Yingzhi Xu,Yuhang Qin
出处
期刊:Environmental Chemistry [CSIRO Publishing]
卷期号:14 (8): 486-486 被引量:23
标识
DOI:10.1071/en17137
摘要

Environmental contextIt is practicable to remediate chlorobenzene-contaminated groundwater by in situ chemical oxidation. This study shows highly efficient degradation of chlorobenzene by an Fe-based process in a wide range of pH values. The technology is feasible for the removal of chlorobenzene from aqueous solutions and is appropriate for remediation of groundwater. AbstractSodium percarbonate (SPC) could be applied as a strong oxidant to degrade organic compounds activated by transition metals. In this study, the degradation performance of chlorobenzene (CB) in the Fe2+-catalysed SPC system was investigated at different Fe2+ and SPC concentrations and pH conditions. Fe2+/Fe3+ conversion was also studied, and the SPC system was compared with the H2O2 and H2O2/Na2CO3 systems. Free radicals were identified through scavenging tests and electron paramagnetic resonance (EPR) experiments, and the reaction intermediates and by-products were determined as well. The results show that CB was completely removed when the molar concentration ratio of Fe2+/SPC/CB was 8 : 8 : 1 and that the decomposition of CB increased as the initial Fe2+/SPC dosage increased. The optimal molar concentration of Fe2+/SPC/CB was 2 : 1 : 1, and the degradation rate was inhibited when increasing or decreasing Fe2+ or SPC. CB degradation was not significantly affected by variation of initial pH, and the variation of pH during the degradation process corresponded well with the degree of Fe2+ to Fe3+ conversion and the formation of •OH. It was confirmed that •OH, O2•− and 1O2 participate in the degradation process. Moreover, not all the •OH takes part in the degradation process, as some transforms into O2•− and 1O2. The same degradation efficiency was obtained when replacing SPC by equal stoichiometric amounts of H2O2, compared with inhibition with the addition of Na2CO3. Further, a likely degradation pathway for CB is proposed based on the identified products. These results show that the Fe2+/SPC system can form the basis of a promising technology for the remediation of CB-contaminated groundwater.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
不可思宇完成签到,获得积分10
刚刚
tyhmugua完成签到,获得积分10
刚刚
five完成签到,获得积分10
1秒前
金甲狮王完成签到,获得积分10
2秒前
Bran完成签到,获得积分10
4秒前
开心向真完成签到,获得积分10
4秒前
ZBM完成签到,获得积分10
4秒前
未来的幻想完成签到,获得积分10
6秒前
王sir完成签到 ,获得积分10
6秒前
7秒前
ltc发布了新的文献求助10
7秒前
张文静完成签到,获得积分10
8秒前
惠JUI完成签到,获得积分10
8秒前
neilphilosci完成签到 ,获得积分10
8秒前
8秒前
楚之杰者完成签到,获得积分10
9秒前
聪明摩托完成签到,获得积分10
10秒前
大方婷冉发布了新的文献求助10
11秒前
盒子应助洽洽瓜子shine采纳,获得10
11秒前
lilian完成签到,获得积分10
11秒前
dui完成签到,获得积分10
12秒前
合适的Y完成签到 ,获得积分20
13秒前
14秒前
16秒前
富贵完成签到 ,获得积分10
16秒前
WJ1989完成签到,获得积分10
16秒前
123发布了新的文献求助10
17秒前
踏雪飞鸿完成签到,获得积分10
17秒前
菠萝汁完成签到,获得积分10
18秒前
rayqiang完成签到,获得积分10
19秒前
i羽翼深蓝i完成签到,获得积分10
19秒前
隋同学完成签到,获得积分10
19秒前
天天快乐应助科研通管家采纳,获得10
19秒前
科研通AI2S应助科研通管家采纳,获得10
19秒前
19秒前
小绵羊完成签到,获得积分20
19秒前
Link完成签到,获得积分10
21秒前
共享精神应助自转无风采纳,获得10
21秒前
Autin完成签到,获得积分10
21秒前
潜放完成签到,获得积分10
22秒前
高分求助中
Lire en communiste 1000
Ore genesis in the Zambian Copperbelt with particular reference to the northern sector of the Chambishi basin 800
Becoming: An Introduction to Jung's Concept of Individuation 600
Communist propaganda: a fact book, 1957-1958 500
Briefe aus Shanghai 1946‒1952 (Dokumente eines Kulturschocks) 500
A new species of Coccus (Homoptera: Coccoidea) from Malawi 500
A new species of Velataspis (Hemiptera Coccoidea Diaspididae) from tea in Assam 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3167282
求助须知:如何正确求助?哪些是违规求助? 2818793
关于积分的说明 7922334
捐赠科研通 2478522
什么是DOI,文献DOI怎么找? 1320396
科研通“疑难数据库(出版商)”最低求助积分说明 632776
版权声明 602443