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Measurement of Vapor Phase Mercury Emissions at Coal-Fired Power Plants Using Regular and Speciating Sorbent Traps with In-Stack and Out-of-Stack Sampling Methods

机译:使用烟囱内和烟囱外采样方法使用常规捕集阱和特定吸附阱测量燃煤电厂的气相汞排放

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摘要

A systematic investigation of sorbent-trap sampling, which is a method that uses paired sorbent traps to measure total vapor phase mercury (Hg), was carried out at two coal-fired power plants. The objective of the study was to evaluate the effects (if any) on data quality when the following aspects of the sorbent trap method are varied: (a) sorbent trap configuration; (b) sampling time; and (c) analytical technique. Also, the performance of a speciating sorbent trap (i.e., a trap capable of separating elemental Hg from oxidized Hg), developed by the Western Kentucky University's Institute for Combustion Science and Environmental Technology (ICSET), was evaluated by direct comparison against the Ontario Hydro (OH) reference method. Flue gas samples were taken using both "regular" and modified sorbent trap measurement systems. The regular sorbent trap systems used a dual-trap, in-stack sampling technique. The modified systems were equipped with either inertial or cyclone probes and used paired, out-of-stack sorbent traps. Both short-term (1.5 h) and long-term (18 h to 10 days) samples were collected. The OH method was run concurrently during the short-term test runs, to provide reference Hg concentrations. At one facility, mercury concentration data from continuous emission monitoring systems were also recorded during the sorbent trap sampling runs. After sampling, the conventional (nonspeciating) sorbent traps were analyzed for Hg, using either a direct combustion method or a wet-chemistry analytical method (i.e., microwave-assisted digestion coupled with cold vapor atomic absorption spectroscopy). The speciating traps were analyzed only by the direct combustion method. All of the sorbent trap data collected in the study were evaluated with respect to relative accuracy, relative deviation of paired traps, and mercury breakthrough. The in-stack and out-of-stack sampling methods produced satisfactory relative accuracy results for both the short-term and long-term testing. For the short-term tests, the in-stack sampling results compared more favorably to the OH method than did the out-of-stack results. The relative deviation between the paired traps was considerably higher for the short-term out-of-stack tests than for the long-term tests. A one-way analysis of variance (ANOVA), showed a statistically significant difference (p < 0.1) between the direct combustion and wet-chemistry analytical methods used in the study; the results from the direct combustion method were consistently higher than the wet-chemistry results. The evaluation of the speciating mercury sorbent trap demonstrated that the trap is capable of providing reasonably accurate total mercury concentrations and speciation data that are somewhat comparable to data obtained with the OH method. Although the results of the study were informative and promising, further evaluation of both the out-of-stack sampling methods and the speciating sorbent trap is recommended.
机译:在两个燃煤电厂对吸附剂捕集器进行了系统的研究,该方法是使用成对的吸附剂捕集器来测量总气相汞(Hg)。本研究的目的是评估吸附剂捕集方法的以下方面变化时对数据质量的影响(如果有):(a)吸附剂捕集器配置; (b)采样时间; (c)分析技术。此外,由西肯塔基大学燃烧科学与环境技术研究所(ICSET)开发的特殊吸附剂捕集阱(即能够从氧化汞中分离出元素汞的捕集阱)的性能通过与安大略水电公司的直接比较进行了评估。 (OH)参考方法。使用“常规”和改进的吸附剂捕集器测量系统采集烟气样品。常规的吸附剂捕集系统使用双重捕集,堆叠式采样技术。改进后的系统配备有惯性或旋风探针,并使用了成对的堆外吸附阱。收集了短期(1.5小时)和长期(18小时至10天)样品。在短期测试运行中同时运行OH方法,以提供参考Hg浓度。在一个设施中,在吸附剂捕集器采样过程中还记录了来自连续排放监测系统的汞浓度数据。采样后,使用直接燃烧法或湿化学分析法(即微波辅助消解结合冷蒸气原子吸收光谱法)分析常规(非特殊)吸附剂阱中的Hg。仅通过直接燃烧法分析了形成陷阱。评估了研究中收集的所有吸附剂捕集阱数据的相对精度,成对捕集阱的相对偏差和汞穿透。对于短期和长期测试,堆内和堆外采样方法均产生令人满意的相对准确度结果。对于短期测试,与栈外结果相比,栈内采样结果比OH方法更具优势。短期堆栈外测试的成对陷阱之间的相对偏差要比长期测试高得多。单向方差分析(ANOVA)显示,研究中使用的直接燃烧和湿化学分析方法之间存在统计学上的显着差异(p <0.1);直接燃烧法的结果始终高于湿化学法的结果。对特定汞吸附剂捕集阱的评估表明,该捕集阱能够提供合理准确的总汞浓度和形态数据,这些数据在某种程度上可与使用OH方法获得的数据相比。尽管研究的结果是有益的和有希望的,但建议进一步评估堆外采样方法和特定的吸附阱。

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  • 来源
    《Energy & fuels》 |2009年第5期|4831-4839|共9页
  • 作者单位

    Institute for Combustion Science and Environmental Technology, Department of Chemistry, Western Kentucky University, 2413 Nashville Road, Bowling Green, Kentucky 42101;

    Institute for Combustion Science and Environmental Technology, Department of Chemistry, Western Kentucky University, 2413 Nashville Road, Bowling Green, Kentucky 42101;

    Institute for Combustion Science and Environmental Technology, Department of Chemistry, Western Kentucky University, 2413 Nashville Road, Bowling Green, Kentucky 42101;

    Department of Chemical Engineering, Ming-Chi University of Technology, 84 Gungjuan RD., Taishan, Taipei, Taiwan 243 R.O.C;

    Department of Chemical Engineering, Ming-Chi University of Technology, 84 Gungjuan RD., Taishan, Taipei, Taiwan 243 R.O.C;

    Department of Chemical Engineering, Ming-Chi University of Technology, 84 Gungjuan RD., Taishan, Taipei, Taiwan 243 R.O.C;

    Department of Chemical Engineering, Ming-Chi University of Technology, 84 Gungjuan RD., Taishan, Taipei, Taiwan 243 R.O.C;

    Department of Chemical Engineering, Ming-Chi University of Technology, 84 Gungjuan RD., Taishan, Taipei, Taiwan 243 R.O.C;

    Department of Chemical Engineering, Ming-Chi University of Technology, 84 Gungjuan RD., Taishan, Taipei, Taiwan 243 R.O.C;

    Institute for Combustion Science and Environmental Technology, Department of Chemistry, Western Kentucky University, 2413 Nashville Road, Bowling Green, Kentucky 42101;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 00:42:21

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