二氧化碳流下褐煤与森林残渣催化共气化的研究

D. Vamvuka, Christia Loulashi
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摘要

本研究调查了两种不同的褐煤与来自希腊北部托勒密盆地地区露天矿土地恢复活动地点收集的森林残留物混合在二氧化碳流下进行的共气化。在气化评估之前,所有样品在固定床单元中进行脱挥发。气化评价使用热分析系统(TG/DTG)在高达1000°C的温度下进行。考察了反应性、转化率、冷气效率以及外源催化剂CaO和K2CO3的影响。林渣的反应速率比褐煤高2 ~ 3倍,前者的转化率达到96.4%(干基),而褐煤的转化率在43.4% ~ 51.6%之间。最大弯曲温度为859 ~ 939℃。褐煤/生物质混合物的反应性比褐煤高,最终转化率提高了约30%。当单个生物炭浸渍30%的CaO或K2CO3时,该过程发生在较低的温度下,褐煤的转化率提高了35% ~ 40%,森林残渣的转化率达到100%。CaO催化剂性能较好。最后,将等量的Kardia褐煤或Ahlada褐煤与含有30% CaO的森林残渣混合配制,分别产生89.6%和71.7%的一氧化碳气体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Catalytic Co-gasification of Lignites Blended with a Forest Residue under the Carbon Dioxide Stream
The present study investigated the co-gasification of two different lignites blended with the forest residue collected from the land restoration activity sites of open-pit mines located in the region of the Ptolemais basin in North Greece performed under the carbon dioxide stream. All samples were devolatilized in a fixed bed unit prior to the gasification evaluations. The gasification evaluations were performed using a thermal analysis system (TG/DTG) operated at temperatures of up to 1000 °C. The reactivity, conversion, cold gas efficiency, and influence of the external catalysts CaO and K2CO3 were assessed in the evaluations. The reaction rate of the forest residue was 2–3 folds higher than that of the lignites, with the conversion of the former reaching a value of 96.4% (dry basis), while the conversion of the lignites varied between 43.4% and 51.6%. The peak inflection temperature was in the range of 859–939 °C. The reactivity of the lignite/biomass blends was higher than that of the lignites, and the final conversion was increased by approximately 30%. When individual biochars were impregnated with 30% CaO or K2CO3, the process occurred at lower temperatures, and the conversion of the lignites increased by 35%–40% while that of the forest residue reached a value of 100%. The CaO catalyst performed better. Finally, a blend of equal amounts of Kardia lignite or Ahlada lignite and the forest residue with 30% CaO was formulated, which resulted in an 89.6% or 71.7% conversion to carbon monoxide gas, respectively.
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