Interactions of Mercury and Other Metals with NOM: Binding by Dissolved OM, Inhibition of Metal Sulfide Precipitation, and Enhancement of Metal Sulfide Dissolution
Interactions of Mercury and Other Metals with NOM: Binding by Dissolved OM, Inhibition of Metal Sulfide Precipitation, and Enhancement of Metal Sulfide Dissolution
批准号:
0447310
负责人:
Kathryn Nagy
金额:
$14.89万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-01 至 2008-08-31
中文摘要
汞在水生系统中的生态命运在很大程度上取决于溶解有机物(DOM)的浓度、无机配体(尤其是硫化物)的浓度以及硫酸盐还原细菌的存在,这些细菌将Hg 2+转化为甲基汞,甲基汞是一种剧毒形式的汞,易于生物累积。最近的研究表明,在环境相关条件下,Hg(II)与DOM的结合强度(KDOM 1023 L kg-1)比以前认为的更强。汞的DOM,这是由一小部分的DOM含有反应性硫醇官能团控制的强结合,是仅次于硫化物相比,其他配体的地球化学意义。除了强结合的汞(II)与DOM的硫醇样部分,强DOM-Hg相互作用是显而易见的DOM的溶解和沉淀的相对不溶性朱砂(HgS)的影响的研究。有机质通过富含芳香族基团的DOM所支持的表面反应增强了HgS的溶解。沉淀的metacinnabar(HgS)被抑制低浓度(=3毫克C L-1)的DOM通过防止纳米胶体硫化汞的聚集。HgS与DOM的相互作用可以通过维持比当前形态模型预测的更高的溶解总汞浓度来影响水生环境中汞的地球化学和生物有效性。(科罗拉多大学博尔德分校)(伊利诺伊大学芝加哥分校)和乔治艾肯(美国地质调查局,博尔德,科罗拉多)概述了一项计划,以调查更具挑战性的方面汞有机物的相互作用。将研究与选定金属(从软到硬)的类似相互作用。这些相互作用的更好的定义是需要改进的金属形态模型和增加了解的因素控制金属在水生系统中的循环。本研究的具体目标是(1)量化有机质、金属性质和硫化物浓度对环境相关浓度下溶解和固体有机质结合金属的影响,(2)阐明有机质中硫、氮和氧官能团对金属结合的贡献,(3)考察了有机质性质对金属硫化物沉淀的抑制作用,重点研究了汞硫化物的抑制作用;(4)探讨了DOM促进金属硫化物溶解的机理。这项研究的主要成果将是确定某些有毒金属在与环境有关的浓度下的有机物质结合常数,并评估胶体稳定化作为一个促使在水生系统中出现溶解金属的过程,拟议研究的更广泛影响包括在国家会议和同行审查的期刊上传播研究结果,此外还有下列特别活动。共同研究员及其研究助理将与广泛使用的地球化学平衡模型(WHAM)的开发者Edward Tipping博士合作,将新的DOM-金属结合常数纳入金属形态计算中,并与Alain Manceau博士合作,描述金属的竞争性结合特征生物修复计划中使用的有机物质。合作PI将开发一个关于有机物与污染物相互作用的研究生课程。从这项研究中得到的信息将直接适用于水生态系统的有效管理,并对生态系统恢复计划具有重要意义。艾肯博士将继续参与美国地质调查局的工作,为管理佛罗里达大沼泽地和加州圣华金-萨克拉门托河三角洲的环境监管机构提供科学依据。
英文摘要
The ecological fate of mercury in aquatic systems depends, in large part, on dissolved organic matter (DOM) concentration, the concentrations of inorganic ligands, especially sulfide, and the presence of sulfate-reducing bacteria that convert Hg2+ into methylmercury, a highly toxic form of mercury that is readily bioaccumulated. Recent research shows that Hg(II) binds to DOM more strongly (KDOM 1023 L kg-1) than previously thought under environmentally relevant conditions. Strong binding of mercury by DOM, which is controlled by a small fraction of the DOM containing reactive thiol functional groups, is second only to sulfide when compared to other ligands of geochemical significance. In addition to strong binding of Hg(II) by thiol-like moieties associated with DOM, strong DOM-Hg interactions are apparent from studies of the effects of DOM on the dissolution and precipitation of relatively-insoluble cinnabar (HgS). Organic matter enhances HgS dissolution through surface reactions favored by DOM rich in aromatic moieties. Precipitation of metacinnabar (HgS) is inhibited by low concentrations (=3 mg C L-1) of DOM by prevention of the aggregation of nanocolloidal mercuric sulfide. Interactions of HgS with DOM can influence the geochemistry and bioavailability of Hg in aquatic environments by maintaining higher dissolved total Hg concentrations than predicted by current speciation models.In this proposal, Joe Ryan (University of Colorado at Boulder), Kathryn Nagy (University of Illinois at Chicago), and George Aiken (U.S. Geological Survey, Boulder, Colorado) outline a plan to investigate more challenging aspects of Hg-organic matter interactions. Similar interactions with selected metals (from soft to hard) will be studied. Better definition of these interactions is required for the improvement of metal speciation models and increased understanding of the factors controlling metal cycling in aquatic systems. Specific objectives of this research are to (1) quantify the effects of organic matter, metal nature, and sulfide concentration on metal binding by dissolved and solid organic matter at environmentally relevant concentrations, (2) elucidate the contributions to metal binding by sulfur, nitrogen, and oxygen functional groups in organic matter, (3) examine the effect of organic matter nature on the inhibition of metal sulfide precipitation, with an emphasis on mercuric sulfide, and (4) probe the mechanism of DOM enhancement of metal-sulfide dissolution. Major products of this research will be the determination of organic matter binding constants for selected toxic metals at environmentally relevant concentrations and the assessment of colloidal stabilization as a process contributing to the occurrence of dissolved metals in aquatic systems.Broader impacts of the proposed research include dissemination of the research results at national conferences and in peer-reviewed journals in addition to the following special activities. The co-PIs and their research assistants will collaborate with Dr. Edward Tipping, developer of a widely used geochemical equilibrium model (WHAM), to incorporate new DOM-metal binding constants into metal speciation calculations and with Dr. Alain Manceau to characterize competitive binding of metals with organic matter used in bioremediation schemes. The co-PIs will develop a graduate class on the interactions of organic matter with contaminants. The information resulting from this study will be directly applicable to the effective management of aquatic ecosystems, and has important implications for ecosystem restoration programs. Dr. Aiken will continue to participate in U.S. Geological Survey efforts to make science accessible for environmental regulators managing the Florida Everglades and the San Joaquin-Sacramento River delta in California.
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会议论文
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批准号:1726335
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项目类别:Standard Grant
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资助金额:$20.99万
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财政年份:2017
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Formation of Kaolinite in Inorganic and Organic Low-Temperature Systems
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项目类别:Continuing Grant
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财政年份:2004
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负责人:Kathryn Nagy
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依托单位:
Formation of Kaolinite in Inorganic and Organic Low-Temperature Systems
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