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Homo- and Heterogeneous Mercury Oxidation in a Bench-Scale Flame-Based Flow Reactor

机译:台式规模火焰流反应器中的均相和异相汞氧化

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摘要

An experimental study of hetero- and homogeneous mercury oxidation chemistry was conducted in a bench-scale flame-based flow reactor with a residence time of 2.9 s. Homogeneous mercury oxidation levels increased with an increasing HCl concentration, with oxidation increasing to 29% at HCl concentrations of 555 parts per million by volume (ppmv). The presence of SO_2 alone also led to Hg oxidation, with approximately 20% oxidation observed at SO_2 concentrations ranging from 100 to 900 ppmv. When both HCl and SO_2 were present, mercury oxidation was enhanced in the presence of SO_2 when the concentration of HCl was 200 ppmv and inhibited when concentration of HCI was 555 ppmv. To examine heterogeneous effects, iron oxide or montmorillonite particles were injected into the post-flame gases of the system. Mercury oxidation by HO was enhanced at high iron oxide particle concentrations (> 100 m~2_(a-Fe_2O_3)of flue gas) compared to the homogeneous system. When iron oxide particles were injected in the presence of 100-400 ppmv SO2 without HCl, mercury oxidation was enhanced at particle loadings less than or equal to 1m~2_(a-Fe_2O_3) of flue gas and decreased with an increasing particle loading. At a SO_2 concentration of 500 ppmv, mercury oxidation increased with an increasing particle concentration. Without HO or SO_2 in the system, mercury oxidation in the presence of iron oxide particles alone was found to be negligible. To determine if the increased oxidation by HCl or SO_2 occurred solely because of an increased surface area, montmorillonite particles were injected, and under these conditions, no increase in the extent of* mercury oxidation was observed, suggesting that iron oxide particle surfaces are an important contributor to the promotion of mercury oxidation in coal combustion systems.
机译:在台式规模的基于火焰的流动反应器中进行了异质和均质汞氧化化学实验研究,其停留时间为2.9 s。均相汞的氧化水平随着HCl浓度的增加而增加,当HCl浓度为百万分之555(ppmv)时,氧化增加到29%。单独存在SO_2也会导致Hg氧化,在浓度范围为100至900 ppmv的SO_2上观察到大约20%的氧化。当同时存在HCl和SO_2时,当HCl浓度为200 ppmv时,在SO_2存在下汞氧化增强,而当HCl浓度为555 ppmv时,汞氧化被抑制。为了检查异质效应,将氧化铁或蒙脱石颗粒注入系统的火焰后气体中。与均相系统相比,在高氧化铁颗粒浓度(> 100 m〜2_(a-Fe_2O_3)烟气)下,HO氧化汞的能力增强。当在没有HCl的100-400 ppmv SO2存在下注入氧化铁颗粒时,汞氧化在小于或等于烟道气的1m〜2_(a-Fe_2O_3)的颗粒负载量下会增强,并随着颗粒负载量的增加而降低。在SO_2浓度为500 ppmv时,汞氧化随着颗粒浓度的增加而增加。在体系中没有HO或SO_2的情况下,仅存在氧化铁颗粒时的汞氧化被忽略不计。为了确定是否仅由于表面积增加而导致HCl或SO_2氧化增加,就注入了蒙脱石颗粒,在这些条件下,没有观察到汞氧化程度的增加,这表明氧化铁颗粒表面是重要的促进了煤燃烧系统中汞的氧化。

著录项

  • 来源
    《Energy & fuels》 |2011年第sepaaocta期|p.4367-4376|共10页
  • 作者单位

    Thayer School of Engineering, Dartmouth College, Hanover, New Hampshire 03755, United States;

    Department of Chemical, Materials, and Biomolecular Engineering, University of Connecticut, Storrs, Connecticut 06269, United States;

    Thayer School of Engineering, Dartmouth College, Hanover, New Hampshire 03755, United States;

  • 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 00:41:38

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