首页> 外文期刊>Chemosphere >Effect of pyrite on enhancement of zero-valent iron corrosion for arsenic removal in water: A mechanistic study
【24h】

Effect of pyrite on enhancement of zero-valent iron corrosion for arsenic removal in water: A mechanistic study

机译:黄铁矿对增强零价铁腐蚀以去除水中砷的作用机理的研究

获取原文
获取原文并翻译 | 示例
           

摘要

In this study, the enhanced effect of pyrite (FeS2) on zero-valent iron (Fe-0) corrosion for arsenic (As) removal was investigated in a combined-Fe-0/FeS2 system. The effects of different Fe-0/FeS2 composition, dosage and initial pH were evaluated by batch experiments. Results showed that the best combination ratio of Fe-0/FeS2 (w/w) was 1:1 and the optimal dosage of mixture was 2.0 g/L. The combination of Fe-0 and FeS2 in a system significantly enhanced the reactivity of Fe-0 for effective As removal within a broad pH range (3.0-9.0). The effective As removal in the combined-Fe-0/FeS2 system was primarily ascribed to being enhanced corrosion of Fe-0 by addition of FeS2. SEM and XRD characterizations strongly verified this point. Specifically, the mechanism study (the releases of Fe2+ and total Fe ion, variations of pH values as well as XPS characterization) suggested that FeS2 in the combined-Fe-0/FeS2 system could alleviate the passivation of Fe-0 (pH(ini) 3.0-5.0) and accelerate the dissolution of pristine oxide film that coated on Fe-0 surface (PHini 6.8-9.0). Besides, FeS2 in combined-Fe-0/FeS2 system could also accelerate the reactions between Fe-0 to O-2 at pH(ini) 3.0-9.0. These phenomena were well explained by a galvanic couple between Fe-0 and FeS2, where FeS2 was a cathode and Fe-0 was an anode. Consequently, electrons released from Fe-0 that mediated by FeS2 to oxide film, passivation layer and O-2 were accelerated in combined-Fe-0/FeS2 system and thereby enhanced the corrosion of Fe-0 for efficient As removal. Our findings suggest that utilizing FeS2 to enhance the corrosion of Fe-0 would be a promising technology for remediation of As-contaminated water. (C) 2019 Elsevier Ltd. All rights reserved.
机译:在这项研究中,在Fe-0 / FeS2组合系统中研究了黄铁矿(FeS2)对零价铁(Fe-0)腐蚀以去除砷(As)的增强作用。通过分批实验评估了不同的Fe-0 / FeS2组成,剂量和初始pH值的影响。结果表明,Fe-0 / FeS2的最佳混合比(w / w)为1:1,最佳混合剂量为2.0 g / L。 Fe-0和FeS2在系统中的组合显着增强了Fe-0在宽广的pH范围(3.0-9.0)中有效去除As的反应性。在Fe-0 / FeS2组合系统中有效去除As的主要原因是通过添加FeS2增强了Fe-0的腐蚀。 SEM和XRD表征强烈证实了这一点。具体而言,机理研究(Fe2 +和总Fe离子的释放,pH值的变化以及XPS表征)表明,Fe-0 / FeS2组合系统中的FeS2可以减轻Fe-0(pH(ini )3.0-5.0)并加速涂在Fe-0表面的原始氧化膜的溶解(PHini 6.8-9.0)。此外,Fe-0 / FeS2组合体系中的FeS2还可以促进pH-0(ini)3.0-9.0时Fe-0至O-2之间的反应。 Fe-0和FeS2之间的电偶很好地解释了这些现象,其中FeS2为阴极,Fe-0为阳极。因此,在Fe-0 / FeS2混合体系中,由Fe-0释放的,由FeS2介导的电子被氧化膜,钝化层和O-2加速,从而增强了Fe-0的腐蚀,从而有效地去除了As。我们的发现表明,利用FeS2增强Fe-0的腐蚀将是一种有前途的技术,用于修复As污染的水。 (C)2019 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Chemosphere》 |2019年第10期|744-753|共10页
  • 作者单位

    South China Univ Technol, Sch Environm & Energy, Guangdong Prov Key Lab Atmospher Environm & Pollu, Guangzhou 510006, Guangdong, Peoples R China;

    South China Univ Technol, Sch Environm & Energy, Guangdong Prov Key Lab Atmospher Environm & Pollu, Guangzhou 510006, Guangdong, Peoples R China|Minist Educ, Key Lab Pollut Control & Ecosyst Restorat Ind Clu, Guangzhou 510006, Guangdong, Peoples R China|South China Univ Technol, State Key Lab Pulp & Paper Engn, Guangzhou 510640, Guangdong, Peoples R China;

    South China Univ Technol, Sch Environm & Energy, Guangdong Prov Key Lab Atmospher Environm & Pollu, Guangzhou 510006, Guangdong, Peoples R China;

    South China Univ Technol, Sch Environm & Energy, Guangdong Prov Key Lab Atmospher Environm & Pollu, Guangzhou 510006, Guangdong, Peoples R China;

    South China Univ Technol, Sch Environm & Energy, Guangdong Prov Key Lab Atmospher Environm & Pollu, Guangzhou 510006, Guangdong, Peoples R China;

    Griffith Univ, Griffith Sch Environm, Environm Futures Res Inst, Ctr Clean Environm & Energy, Gold Coast Campus, Gold Coast, Qld 4222, Australia;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Zero-valent iron; Pyrite; Enhanced corrosion; Arsenic removal;

    机译:零价铁;硫铁矿;增强腐蚀;除砷;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号