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Parametric Study on the CO_2 Capture Capacity of CaO-Based Sorbents in Looping Cycles

机译:循环中CaO基吸附剂CO_2捕集能力的参数研究

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An experimental parametric study on the CO_2 capture activity of four limestone-derived CaO-based sorbents has been performed. Experiments were done in a thermogravimetric analyzer (TGA) at temperatures ranging from 650 to 850 ℃. Three particle-size fractions of Kelly Rock limestone and powders obtained by their grinding were also tested, while the influence of carbonation and calcination durations was examined at 750 and 850 ℃. Calcination is typically performed in an atmosphere of N_2 and carbonation in 50% CO_2 (N_2 balance), and the influence of the effective CO_2 concentration surrounding reacting particles was examined by changing the sample mass in some experiments. The results indicated that increasing the calcination/carbonation temperature had a negative influence on the sorbent activity, while the influence of particle size was small, although larger particles have higher activity. This was unexpected, but it can be explained by the higher content of impurities in the smaller particles. Grinding enhances sorbent activity, and this appears to be more than simply due to increased external surface area of the sorbent particles in the powdered samples. Prolonged carbonation time has a negative effect on the sorbent performance. The formation and decomposition of CaCO_3 as well as its presence on the sorbent surface at higher temperatures appear to be key factors in the loss of surface area (i.e., decrease in sorbent activity). However, it is shown that the prolonged exposure to calcination conditions employed in this work (inert atmosphere) has a slightly beneficial effect on sorbent behavior as a function of the number of calcination/carbonation cycles. Experiments with larger sample masses typically resulted in better conversions. Analysis of scanning electron microscope (SEM) images of spent sorbent particles obtained from different reactor types indicated that thermal stresses are the main cause for sorbent particle fracture and attrition.
机译:已对四种石灰石衍生的CaO基吸附剂的CO_2捕集活性进行了实验参数研究。实验在热重分析仪(TGA)中进行,温度范围为650至850℃。还测试了Kelly Rock石灰石的三种粒度级分和通过研磨得到的粉末,并在750和850℃下研究了碳化和煅烧时间的影响。煅烧通常在N_2气氛下进行,并在50%CO_2(N_2平衡)下进行碳酸化,在某些实验中,通过改变样品质量来检查反应颗粒周围有效CO_2浓度的影响。结果表明,提高煅烧/碳酸化温度对吸附剂活性具有负面影响,而粒径的影响较小,尽管较大的颗粒具有较高的活性。这是出乎意料的,但是可以用较小颗粒中较高的杂质含量来解释。研磨增强了吸附剂的活性,这似乎不仅仅是由于粉末状样品中吸附剂颗粒的外表面积增加而引起的。延长碳酸化时间会对吸附性能产生负面影响。 CaCO 3的形成和分解以及其在较高温度下在吸附剂表面上的存在似乎是表面积损失(即吸附剂活性降低)的关键因素。但是,已表明,在这项工作中使用的长时间暴露于煅烧条件(惰性气氛),对煅烧/碳酸化循环次数的函数,对吸附剂的行为有轻微的有利影响。使用更大质量的样品进行实验通常会带来更好的转化率。从不同反应器类型获得的废吸附剂颗粒的扫描电子显微镜(SEM)图像分析表明,热应力是造成吸附剂颗粒破裂和磨损的主要原因。

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  • 来源
    《Energy & fuels》 |2008年第3期|p.1851-1857|共7页
  • 作者单位

    CANMET Energy Technology Centre-Ottawa, Natural Resources Canada, 1 Haanel Drive, Ottawa, Ontario, Canada K1A 1M1;

  • 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
  • 中图分类 TK-;
  • 关键词

  • 入库时间 2022-08-18 00:42:37

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