半碳化处理对生物质和煤炭联合气化的影响研究

IF 0.8 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Solid Fuel Chemistry Pub Date : 2024-03-20 DOI:10.3103/S0361521923080074
Wu Chengli, Shen Shuhao, Li Hanxu, Fan Honggui, Gui Guoyang
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引用次数: 0

摘要

摘要 巨大的能源需求导致煤炭大量消耗,造成严重的资源和环境问题。生物质能源资源丰富,对环境影响小,可再生,开发潜力大。但由于其固有的缺点,难以大规模利用。通过热解对生物质进行预处理,可以显著改善其性能。同时,生物质与煤的共气化可以充分发挥煤的高能量密度和生物质的高反应活性的优势,弥补单独气化的不足。这对于大规模工业化利用生物质能源、优化我国能源结构具有重要意义。本文以玉米秸秆、水稻秸秆、小麦秸秆和烟煤为实验材料。首先,在 200-600°C 下对生物质进行半碳化,研究生物质结构和化学性质的变化。然后,利用热分析技术研究了半碳化生物质和生物质-煤混合物的 CO2 反应特性,并进一步探讨了其协同作用机理。随着热解温度的升高,半碳化生物质的固定碳和挥发物含量增加,挥发物减少,O/C 和 H/C 原子比降低,生物质的煤化程度转变为无烟煤。利用扫描电子显微镜(SEM)、比表面积、傅立叶变换红外吸收光谱(FTIR)等对生物质的化学特性进行了研究。结果表明,生物质中的极性官能团不断减少,芳香度不断提高,碳结构更加稳定,耐热性增强。更高的固定碳含量和更稳定的碳结构提高了非等温气化过程的起始温度、终止温度和最大失重率;等温气化实验表明,低温(200-300℃)制备的生物质样品的气化性能略高于原料样品,而中高温(400-600℃)生物质碳的气化性能低于原料样品。气化性能的差异是碳结构稳定性和生物质中碱金属含量共同作用的结果。利用扫描电子显微镜-能量色散 X 射线光谱(SEM-EDX)研究了共热解焦炭和气化残渣的理化结构。结果表明,共热解焦炭的芳香度下降,芳香层的堆积高度降低。半焦中的碱金属阻碍了共热解焦的有序化过程,抑制了石墨化,碱金属在煤焦表面积累,在气化过程中与碳基质反应,成为气化反应的活性中心,促进了共气化反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Study on Influence of Semi-carbonization Treatment on Co-gasification of Biomass and Coal

The huge demand for energy has led to the massive consumption of coal, causing serious resource and environmental problems. Biomass energy resources are abundant, have a small impact on the environment, are renewable, and have great development potential. However, due to their inherent disadvantages, they are difficult to use on a large scale. Pre-treating biomass through pyrolysis can significantly improve its performance. At the same time, co-gasification of biomass and coal can fully exploit the advantages of high energy density of coal and high reactivity of biomass, making up for the shortcomings of gasification alone. This is of great significance for the industrial utilization of biomass energy on a large scale and the optimization of China’s energy structure. In this paper, corn stalks, rice straw, wheat straw and bituminous coal were used as experimental materials. Firstly, biomass was semi-carbonized at 200–600°C, and the changes in the structure and chemical properties of biomass were investigated. Then, thermal analysis technology was used to study the CO2 reaction characteristics of semi-carbonized biomass and biomass-coal mixture, and further explore the synergistic mechanism.

As the pyrolysis temperature increased, the fixed carbon and volatile content of semi-carbonized biomass increased, volatile matter decreased, O/C and H/C atomic ratios decreased, and the degree of coalification of biomass was transformed into anthracite. The chemical characteristics of biomass were studied using scanning electron microscopy (SEM), specific surface area, Fourier transform infrared absorption spectroscopy (FTIR), etc. The results showed that the polar functional groups in biomass decreased continuously, aromaticity increased continuously, carbon structure became more stable, and heat resistance increased. Higher fixed carbon content and more stable carbon structure increased the starting temperature, ending temperature and maximum weight loss rate of non-isothermal gasification process; isothermal gasification experiments determined that the gasification performance of biomass samples prepared at low temperature (200–300°C) would be slightly higher than that of raw samples, while the gasification performance of medium-high temperature (400–600°C) biomass carbon was lower than that of raw samples. The difference in gasification performance was the result of the combined effect of carbon structure stability and alkali metal content in biomass. Scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDX) was used to study the physicochemical structure of co-pyrolysis coke and gasification residue. The results showed that the aromaticity of co-pyrolysis coke decreased and the stacking height of aromatic layers decreased. Alkali metals in semi-coke hindered the ordering process of co-pyrolysis coke, inhibited graphitization, and alkali metals accumulated on the surface of coal coke and reacted with carbon matrix during gasification process to become active centers for gasification reaction, promoting co-gasification reaction.

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来源期刊
Solid Fuel Chemistry
Solid Fuel Chemistry CHEMISTRY, MULTIDISCIPLINARY-ENERGY & FUELS
CiteScore
1.10
自引率
28.60%
发文量
52
审稿时长
6-12 weeks
期刊介绍: The journal publishes theoretical and applied articles on the chemistry and physics of solid fuels and carbonaceous materials. It addresses the composition, structure, and properties of solid fuels. The aim of the published articles is to demonstrate how novel discoveries, developments, and theories may be used in improved analysis and design of new types of fuels, chemicals, and by-products. The journal is particularly concerned with technological aspects of various chemical conversion processes and includes papers related to geochemistry, petrology and systematization of fossil fuels, their beneficiation and preparation for processing, the processes themselves, and the ultimate recovery of the liquid or gaseous end products.
期刊最新文献
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