Taewoo Lee , Sangyoon Lee , Yiu Fai Tsang , Eilhann E. Kwon
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引用次数: 0
摘要
木质纤维素生物质通常通过选择性转化生物质中的糖类转化为生物燃料,留下相当数量的木质素作为废物。热解是高效利用原料的另一种解决方案;然而,由于生物原油的成分异质性,生物原油的燃料使用面临着挑战。因此,生物质热解转化为合成气可以在可控的等效比下有效燃烧。本研究的重点是提高木质纤维素生物质,如核桃壳(WNSs)的热解合成气产量,同时利用二氧化碳作为部分氧化剂。在热解过程中,CO2与wns衍生的挥发性化合物反应,将其转化为富含co的合成气。在≥520°C时观察到CO2驱动的CO增强,需要采取措施加速CO2反应动力学。因此,考察了包括测试温度和CO2组成在内的操作参数,以优化催化热解过程中CO2的反应性。为了评估工业适用性,将合成的富含CO的合成气应用于燃气轮机系统的发电。在最佳条件下(80 vol% CO2和700°C),理论计算能够估计净涡轮功为1882.5 MJ s - 1,热效率为76.18%,与参考天然气相比增加了2.71倍和3.01倍。
Carbon-negative power generation using syngas produced from CO2-cofeeding pyrolysis of lignocellulosic biomass
Lignocellulosic biomass is typically converted into biofuels through selective conversion of saccharides in the biomass, leaving considerable amounts of lignin as waste. Pyrolysis is an alternative solution for efficient feedstock utilization; however, the fuel use of biocrude face challenges due to their compositional heterogeneity. Thus, the pyrolytic conversion of biomass into syngas could be practical for efficient combustion under manageable equivalent ratios. This study focuses on enhancing syngas production from the pyrolysis of lignocellulosic biomass, such as walnut shells (WNSs), while leveraging CO2 as a partial oxidant. During pyrolysis, CO2 reacted with WNS-derived volatile compounds, converting them into CO-rich syngas. The CO2-driven CO enhancement was observed at ≥ 520 °C, requiring measures to accelerate CO2 reaction kinetics. Therefore, operational parameters, including test temperature and CO2 composition, were scrutinized to optimize CO2 reactivity during catalytic pyrolysis. To assess industrial applicability, the resultant syngas enriched with CO was applied for power generation in a gas-turbine system. Under optimal conditions (80 vol% CO2 and 700 °C), theoretical calculations enabled to estimate 1882.5 MJ s−1 of net turbine work and 76.18 % of thermal efficiency, revealing 2.71- and 3.01-fold increases compared to reference natural gases.
期刊介绍:
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