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Bench-scale gasification of cedar wood - Part II: Effect of Operational conditions on contaminant release

机译:雪松木的台式气化-第二部分:操作条件对污染物释放的影响

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摘要

Here, we present the evolution profile of tar in the product gas during cedar biomass gasification. We also discuss the evolution of other contaminants (H_2S, COS, NH_3, HCN, and HC1). The cedar wood was gasified under various operating conditions in a bench-scale externally heated updraft gasifier; this was followed by thermal reforming. Tar levels in the product gas were significantly affected by the operating conditions used. At a gasification temperature of 923 K, there was no clear relation between the evolution of phenolic tar in the product gas as a function of residence time. The evolution of PAH tar at a low gasification temperature was lower than the evolution of phenolic tar. With increasing temperature, the proportion of PAH tar content became significant. At a gasification temperature of 1223 K, increasing the residence time reduced the content of PAH tar owing to a catalytic effect associated with ash generation at high temperatures. Increasing the steam-to-carbon (S/C) ratio under thermal conditions had a slight effect on PAH conversion. However, increasing the equivalence ratio (ER) effectively reduced the tar levels. The conversion of fuel-sulfur and fuel-nitrogen to volatile-sulfur and volatile-nitrogen, respectively, increased with increasing S/C ratio and ER. The evolutions of COS and HCN gases were much smaller than the evolution of H_2S and NH_3. The evolution of HCl in the product gas decreased slightly with increasing ER. Increasing the S/C ratio decreased the HCl levels in the product gas. The effect of temperature on contaminant levels could not be fully understood due to limited availability of experimental data at various temperatures. We also compare our findings with data in the literature.
机译:在这里,我们介绍了柏木生物质气化过程中产物气中焦油的演变过程。我们还讨论了其他污染物(H_2S,COS,NH_3,HCN和HCl)的演变。在各种规模的操作条件下,将雪松木放在台式规模的外部加热的上升气流式气化炉中进行气化;然后进行热重整。产物气中的焦油含量受所用操作条件的影响很大。在923 K的气化温度下,产物气中酚焦油的释放与停留时间的函数之间没有明确的关系。在低气化温度下,PAH焦油的释放量低于酚醛焦油的释放量。随着温度升高,PAH焦油含量的比例变得显着。在1223 K的气化温度下,由于与高温下产生灰分相关的催化作用,增加停留时间会降低PAH焦油的含量。在热条件下提高蒸汽碳比(S / C)对PAH转化率有轻微影响。但是,增加当量比(ER)有效降低了焦油含量。随着S / C比和ER的增加,燃料硫和燃料氮分别转化为挥发性硫和挥发性氮的转化率增加。 COS和HCN气体的逸出量远小于H_2S和NH_3的逸出量。随着ER的增加,产物气中HCl的释放量略有减少。提高S / C比会降低产物气中的HCl含量。由于各种温度下的实验数据有限,无法完全理解温度对污染物水平的影响。我们还将我们的发现与文献数据进行比较。

著录项

  • 来源
    《Chemosphere》 |2013年第4期|1501-1507|共7页
  • 作者单位

    Department of Chemical Engineering, College of Engineering, Mutah University, Karak 61710, Jordan;

    Center for Material Cycles and Waste Management Research, National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki 305-8506, Japan;

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

    ammonia; chlorine; biomass; gasification; sulfur; tar;

    机译:氨;氯;生物质气化;硫;柏油;

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