首页> 外文期刊>Environmental Science & Technology >Dissolved Organic Matter Affects Arsenic Mobility and Iron(Ⅲ) (hydr)oxide Formation: Implications for Managed Aquifer Recharge
【24h】

Dissolved Organic Matter Affects Arsenic Mobility and Iron(Ⅲ) (hydr)oxide Formation: Implications for Managed Aquifer Recharge

机译:溶解的有机物影响砷的迁移和氧化铁(Ⅲ)的形成:对蓄水层补给的意义

获取原文
获取原文并翻译 | 示例
       

摘要

During managed aquifer recharge (MAR), injected water significantly alters water chemistry in an aquifer, affecting arsenic mobility. To elucidate the effects of dissolved organic matter (DOM) on arsenic mobilization during MAR, this bench-scale study examined arsenic mobilization from arsenopyrite (FeAsS, an arsenic-containing sulfide) in the presence of Suwannee River natural organic matter, humic acid, and fulvic acid (SRNOM, SRHA, and SRFA), alginate (Alg), polyaspartate (PA), and glutamate (Glu). Suwannee River DOM (SRDOM) decreased arsenic mobility in the short term (<6 h) via inhibiting arsenopyrite oxidative dissolution, but increased arsenic mobility over a longer experimental time (similar to 7 days) via inhibiting secondary iron(III) (hydr)oxide precipitation and decreasing arsenic adsorption onto iron(III) (hydr)oxide. In situ grazing incidence small-angle X-ray scattering measurements indicated that SRDOM decreased iron(III) (hydr)oxide nucleus sizes and growth rates. A combined analysis of SRDOM and other proteinaceous or labile DOM (Alg, PA, and Glu) revealed that DOM with higher molecular weights would cause more increased arsenic mobility. These new observations advance our understanding of the impacts of DOM in injected water on arsenic mobility and secondary precipitate formation during MAR, and in other systems where interactions between DOM, arsenic, and iron(III) (hydr)oxides take place.
机译:在受控含水层补给(MAR)期间,注入的水会显着改变含水层中的水化学性质,从而影响砷的迁移率。为阐明溶解有机物(DOM)对MAR期间砷移动的影响,这项基准规模研究研究了在Suwannee河天然有机物,腐殖酸和四氢呋喃存在下从毒砂(FeAsS,一种含砷的硫化物)中砷的移动。富里酸(SRNOM,SRHA和SRFA),藻酸盐(Alg),聚天冬氨酸(PA)和谷氨酸(Glu)。 Suwannee River DOM(SRDOM)通过抑制毒砂黄铁矿的氧化溶解而在短期内(<6 h)降低了砷的迁移率,但在较长的实验时间内(类似于7天)通过抑制次要铁(III)(氢氧化)的氧化物提高了砷的迁移率。沉淀并减少砷吸附在三氧化二铁上的吸附。原位放牧入射角的小角度X射线散射测量表明SRDOM降低了铁(III)(氢)氧化物核的大小和生长速率。对SRDOM和其他蛋白质或不稳定DOM(Alg,PA和Glu)的组合分析显示,分子量较高的DOM会引起更多的砷迁移。这些新发现使我们对注入水中的DOM对MAR期间砷迁移率和二次沉淀物形成以及其他在DOM,砷和三价铁氧化物之间发生相互作用的系统的影响的理解。

著录项

  • 来源
    《Environmental Science & Technology》 |2019年第24期|14357-14367|共11页
  • 作者单位

    Washington Univ Dept Energy Environm & Chem Engn St Louis MO 63130 USA;

    Washington Univ Dept Energy Environm & Chem Engn St Louis MO 63130 USA|Missouri Univ Sci & Technol Dept Geol Engn Rolla MO 65409 USA;

    Washington Univ Dept Energy Environm & Chem Engn St Louis MO 63130 USA|MIT Dept Civil & Environm Engn 77 Massachusetts Ave Cambridge MA 02139 USA;

    Argonne Natl Lab Xray Sci Div 9700 S Cass Ave Argonne IL 60439 USA;

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

  • 入库时间 2022-08-18 05:04:56

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