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Mercury transformation and speciation in flue gases from anthropogenic emission sources: a critical review

机译:人为排放源产生的烟气中汞的转化和形态分析:一项重要评论

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摘要

Mercury transformation mechanisms and speciation profiles arereviewed for mercury formed in and released from flue gases of coal-firedboilers, non-ferrous metal smelters, cement plants, iron and steel plants, waste incinerators, biomass burning and so on. Mercury in coal,ores, and other raw materials is released to flue gases in the form ofHg during combustion or smelting in boilers, kilns or furnaces.Decreasing temperature from over 800 °C to below 300 °Cin flue gases leaving boilers, kilns or furnaces promotes homogeneous andheterogeneous oxidation of Hg to gaseousdivalent mercury (Hg), with a portion of Hg adsorbed onto flyash to form particulate-bound mercury (Hg). Halogen is the primaryoxidizer for Hg in flue gases, and active components (e.g., TiO,FeO, etc.) on fly ash promote heterogeneous oxidation andadsorption processes. In addition to mercury removal, mercury transformationalso occurs when passing through air pollution control devices (APCDs),affecting the mercury speciation in flue gases. In coal-fired power plants,selective catalytic reduction (SCR) system promotes mercury oxidation by34–85 %, electrostatic precipitator (ESP) and fabric filter (FF) removeover 99 % of Hg, and wet flue gas desulfurization system (WFGD)captures 60–95 % of Hg. In non-ferrous metal smelters, mostHg is converted to Hg and removed in acid plants (APs). Forcement clinker production, mercury cycling and operational conditionspromote heterogeneous mercury oxidation and adsorption. The mercuryspeciation profiles in flue gases emitted to the atmosphere are determinedby transformation mechanisms and mercury removal efficiencies by variousAPCDs. For all the sectors reviewed in this study, Hg accounts forless than 5 % in flue gases. In China, mercury emission has a higherHg fraction (66–82 % of total mercury) in flue gases from coalcombustion, in contrast to a greater Hg fraction (29–90 %) fromnon-ferrous metal smelting, cement and iron and/or steel production. The higherHg fractions shown here than previous estimates may imply strongerlocal environmental impacts than previously thought, caused by mercuryemissions in East Asia. Future research should focus on determining mercuryspeciation in flue gases from iron and steel plants, waste incineration andbiomass burning, and on elucidating the mechanisms of mercury oxidation andadsorption in flue gases.
机译:综述了燃煤锅炉,有色金属冶炼厂,水泥厂,钢铁厂,垃圾焚烧炉,生物质燃烧等中烟气中形成和释放的汞的汞转化机理和形态分布。煤,矿石和其他原材料中的汞在锅炉,窑炉或熔炉中燃烧或熔融过程中以汞的形式释放到烟道气中。从锅炉,窑炉或窑炉中排出的烟气温度从800摄氏度降低到300摄氏度以下促进汞的均质和异质氧化为气态二价汞(Hg),并将一部分汞吸附到粉煤灰上,形成结合颗粒的汞(Hg)。卤素是烟气中Hg的主要氧化剂,粉煤灰中的活性成分(例如TiO,FeO等)促进了异质氧化和吸附过程。除除汞外,通过空气污染控制装置(APCD)时还会发生汞转化,从而影响烟道气中的汞形态。在燃煤电厂中,选择性催化还原(SCR)系统可将汞氧化提高34%至85%,静电除尘器(ESP)和织物过滤器(FF)可去除99%以上的汞,而湿法烟气脱硫系统(WFGD)则可捕获60 –95%的汞在有色金属冶炼厂中,大多数汞会转化为汞,并在酸工厂(AP)中去除。强制熟料生产,汞循环和运行条件促进了异质汞的氧化和吸附。排放到大气中的烟道气中的汞形态由各种APCD的转化机制和除汞效率决定。对于本研究中所审查的所有部门,汞在烟气中的含量不足5%。在中国,燃煤烟气中的汞排放具有较高的汞含量(占总汞的66-82%),而有色金属冶炼,水泥,铁和/或钢的汞排放具有较高的汞含量(29-90%)生产。此处显示的汞含量高于先前的估计值,可能暗示东亚地区的汞排放给当地环境带来的影响要比以前认为的要强。未来的研究应侧重于确定钢铁厂烟气中的汞形态,废物焚烧和生物质燃烧,并阐明汞氧化和烟气吸附机理。

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