自动生成先进生物燃料的燃烧机理:二乙醚案例研究

IF 1.5 4区 化学 Q4 CHEMISTRY, PHYSICAL
Christian A. Michelbach, Alison S. Tomlin
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引用次数: 0

摘要

先进生物燃料有可能取代相当一部分传统液体化石燃料。然而,根据所选原料和生产工艺的不同,潜在化合物的范围可能很广。人们对许多此类燃料的发动机相关行为了解不够,尤其是在复杂的混合燃料中使用时。模拟工具可以帮助探索此类混合燃料的燃烧行为,但需要依靠强大的化学机制,才能在热化学空间的大范围内对性能目标进行准确预测。自动机理生成(AMG)等工具可以帮助生成合适的机理。此类工具通常用于生成描述非含氧、非芳香烃氧化的机理,但由于生物燃料中含有含氧官能团,因此生物燃料的出现增加了新的挑战。本研究以二乙醚 (DEE) 为例,研究了 AMG 工具反应机理生成器在此类任务中的能力。研究提出了一种生成高级生物燃料机理的方法,并根据文献来源的实验测量结果对点火延迟时间、喷射搅拌反应器物种浓度和火焰速度进行了评估,实验条件包括 φ = 0.5-2.0、P = 1-100 巴和 T = 298-1850 K。需要高质量的燃料特定反应速率和含氧物种的热化学,还需要一个种子机理、一个热化学库,并扩展反应族数据库以包括含氧化合物的训练数据。最终的 DEE 机理包含 146 个物种和 4392 个反应,总体而言,在所调查的目标数据中,与文献来源的机理相比,DEE 预测更为准确或具有可比性。为其他潜在的先进生物燃料成分生成燃烧机理可以很容易地利用这些数据库更新,减少未来用户干预的需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Automatic mechanism generation for the combustion of advanced biofuels: A case study for diethyl ether

Automatic mechanism generation for the combustion of advanced biofuels: A case study for diethyl ether

Advanced biofuels have the potential to supplant significant fractions of conventional liquid fossil fuels. However, the range of potential compounds could be wide depending on selected feedstocks and production processes. Not enough is known about the engine relevant behavior of many of these fuels, particularly when used within complex blends. Simulation tools may help to explore the combustion behavior of such blends but rely on robust chemical mechanisms providing accurate predictions of performance targets over large regions of thermochemical space. Tools such as automatic mechanism generation (AMG) may facilitate the generation of suitable mechanisms. Such tools have been commonly applied for the generation of mechanisms describing the oxidation of non-oxygenated, non-aromatic hydrocarbons, but the emergence of biofuels adds new challenges due to the presence of functional groups containing oxygen. This study investigates the capabilities of the AMG tool Reaction Mechanism Generator for such a task, using diethyl ether (DEE) as a case study. A methodology for the generation of advanced biofuel mechanisms is proposed and the resultant mechanism is evaluated against literature sourced experimental measurements for ignition delay times, jet-stirred reactor species concentrations, and flame speeds, over conditions covering φ = 0.5–2.0, P = 1–100 bar, and T = 298–1850 K. The results suggest that AMG tools are capable of rapidly producing accurate models for advanced biofuel components, although considerable upfront input was required. High-quality fuel specific reaction rates and thermochemistry for oxygenated species were required, as well as a seed mechanism, a thermochemistry library, and an expansion of the reaction family database to include training data for oxygenated compounds. The final DEE mechanism contains 146 species and 4392 reactions and in general, provides more accurate or comparable predictions when compared to literature sourced mechanisms across the investigated target data. The generation of combustion mechanisms for other potential advanced biofuel components could easily capitalize on these database updates reducing the need for future user interventions.

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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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