用于燃料气生产的乙醇超临界水气化

Brian R. Pinkard, Elizabeth G. Rasmussen, J. Kramlich, P. Reinhall, I. Novosselov
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引用次数: 2

摘要

工业规模的稀乙醇超临界水气化有望为联合循环发电厂提供可持续的生物合成气生产途径。具有成本效益的生物合成气生产将减少对化石燃料发电的依赖,并通过利用废弃生物质资源减少温室气体排放。连续超临界水气化在不添加催化剂的情况下,在短停留时间内提供高反应物转化率。在连续反应器中研究了乙醇在超临界水中的分解,温度为560℃,温度为25 MPa,停留时间为3 ~ 8 s,初始乙醇浓度为8.1 wt%。高分辨率,原位拉曼光谱有助于识别反应产物。H2、CO和CH4的显著产率表明在研究条件下脱氢反应途径占主导地位,乙烷的少量产率表明二次脱水反应途径占主导地位。乙烯产率几乎不存在,这表明在这些条件下乙烯迅速加氢成乙烷。乙醇脱氢生成H2、CO和CH4的总体燃料价值提升为84.5 kJ/mol-EtOH。乙醇脱水为乙烷导致燃料的总体降解为−3.8 kJ/mol-EtOH。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Supercritical Water Gasification of Ethanol for Fuel Gas Production
Supercritical water gasification of dilute ethanol at the industrial scale promises a sustainable route to bio-syngas production for use in combined cycle power plants. Cost-effective bio-syngas production would reduce reliance on fossil fuels for electricity generation and reduce greenhouse gas emissions by utilizing waste biomass resources. Continuous supercritical water gasification offers high reactant conversion at short residence times without an added catalyst. The decomposition of ethanol in supercritical water is studied in a continuous reactor at 560 °C, 25 MPa, residence times between 3 and 8 s, and a constant initial ethanol concentration of 8.1 wt%. High-resolution, in-situ Raman spectroscopy facilitates identification of reaction products. Significant yields of H2, CO, and CH4 indicate the dominance of a dehydrogenation reaction pathway at studied conditions, while minor yields of ethane indicate a secondary dehydration reaction pathway. Ethylene yields are virtually nonexistent, indicating rapid hydrogenation of ethylene to ethane at these conditions. Ethanol dehydrogenation to H2, CO, and CH4 results in an overall fuel value upgrade of 84.5 kJ/mol-EtOH. Dehydration of ethanol to ethane results in an overall fuel degradation of −3.8 kJ/mol-EtOH.
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