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High temperature interactions of alkali vapors with solids during coal combustion and gasification.

机译:煤燃烧和气化过程中碱蒸气与固体的高温相互作用。

摘要

The high temperature interactions of alkali metal compounds with solids present in coal conversion processes are investigated. A temperature and concentration programmed reaction method is used to investigate the mechanism by which organically bound alkali is released from carbonaceous substrates. Vaporization of the alkali is preceded by reduction of oxygen-bearing groups during which CO is generated. A residual amount of alkali remains after complete reduction. This residual level is greater for potassium, indicating that potassium has stronger interactions with graphitic substrates than sodium. Other mineral substrates were exposed to high temperature alkali chloride vapors under both nitrogen and simulated flue gas atmospheres to investigate their potential application as sorbents for the removal of alkali from coal conversion flue gases. The compounds containing alumina and silica are found to readily adsorb alkali vapors and the minerals kaolinite, bauxite and emathlite are identified as promising alkali sorbents. The fundamentals of alkali adsorption on kaolinite, bauxite and emathlite are compared and analyzed both experimentally and through theoretical modeling. The experiments were performed in a microgravimetric reactor system; the sorbents were characterized before and after alkali adsorption using scanning Auger microscopy, X-ray diffraction analysis, mercury porosimetry and atomic emission spectrophotometry. The results show that the process is not a simple physical condensation, but a complex combination of several diffusion steps and reactions. There are some common features among these sorbents in their interactions with alkali vapors: In all cases the process is diffusion influenced, the rate of adsorption decreases with time and there is a final saturation limit. However, there are differences in reaction mechanisms leading to potentially different applications for each sorbent. Bauxite and kaolinite react with NaCl and water vapor to form nephelite and carnegieite and release HCl to the gas phase. However, emathlite reacts to form albite and HCl vapor. Albite has a melting point significantly lower than nephelite and carnegieite; therefore, emathlite is more suitable for lower temperature sorption systems downstream of the combustors/gasifiers, while kaolinite and bauxite are suitable as in-situ additives.
机译:研究了碱金属化合物与煤转化过程中存在的固体之间的高温相互作用。使用温度和浓度编程的反应方法来研究从碳质底物中释放有机结合的碱的机理。在碱汽化之前,先还原含氧基团,在此期间生成CO。完全还原后,残留有碱。钾的残留水平更高,表明钾与石墨底物的相互作用强于钠。其他矿物基质在氮气和模拟烟气气氛下均暴露于高温碱金属氯化物蒸汽中,以研究其潜在的应用作为吸附剂,以从煤炭转化烟气中脱除碱。发现含有氧化铝和二氧化硅的化合物易于吸附碱蒸汽,矿物高岭石,铝土矿和玄武岩被认为是有前途的碱吸附剂。通过实验和理论建模,比较和分析了碱在高岭石,铝土矿和玄武岩上吸附的基本原理。实验在微重力反应器系统中进行。通过扫描俄歇显微镜,X射线衍射分析,汞孔隙率法和原子发射分光光度法对碱吸附前后的吸附剂进行了表征。结果表明,该过程不是简单的物理冷凝,而是几个扩散步骤和反应的复杂组合。这些吸附剂与碱蒸气的相互作用具有一些共同的特征:在所有情况下,该过程都受到扩散的影响,吸附速率随时间降低,并且存在最终的饱和极限。但是,反应机理存在差异,导致每种吸附剂的潜在用途不同。铝土矿和高岭石与NaCl和水蒸气反应形成软玉和卡耐基石,并向气相中释放HCl。但是,辉石起反应生成钠长石和HCl蒸气。阿尔比特的熔点明显低于霞石和卡耐基石。因此,天青石更适合于燃烧器/气化炉下游的低温吸附系统,而高岭石和铝土矿则适合作为原位添加剂。

著录项

  • 作者

    Punjak Wayne Andrew;

  • 作者单位
  • 年度 1988
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
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