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Laminar Flame Speed, Markstein Length and Flame Chemistry of the Butanol Isomers from 1 atm to 5 atm

机译:Laminar火焰速度,Markstein长度和丁醇异构体的火焰化学从1atm到5atm的丁醇异构体

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Laminar flame speeds and Markstein lengths for n-butanol, s-butanol, i-butanol and t-butanol at pressures from 1 atm to 5 atm were experimentally measured in a heated, dual-chamber vessel. Results at all pressures show that n-butanol has the highest flame speeds, followed by s-butanol and i-butanol, and then t-butanol, which quantitatively agree reasonably well with the computed results using the recent mechanism of Sarathy and co-authors. Results further show that while the isomers have different Markstein lengths, they have similar Markstein numbers which is the appropriate nondimensional parameter to quantify flame stretch. Investigations on thermal effects, reaction rate sensitivities, intermediate species distributions and reaction paths subsequently demonstrate that kinetic effect is the primary reason for the ordering of the flame speed. Specifically, since s-butanol, i-butanol and t-butanol all have branched molecular structures, they crack into relatively stable branched intermediate species, such as iso-butene, iso-propenol and acetone, with the resulting flame speeds depending on the extent of fuel molecule branching.
机译:在加热的双室容器中,在1atm至5atm的压力下,在加热的双腔容器中测量压力下正丁醇,S-丁醇,叔丁醇和叔丁醇的层状火焰速度和Markstein长度。所有压力的结果表明,正丁醇具有最高的火焰速度,其次是S-丁醇和叔丁醇,然后是叔丁醇,其使用最近的SARATHY和共同作者的机制可以合理地与计算结果相当良好。 。结果进一步表明,虽然异构体具有不同的Markstein长度,但它们具有类似的Markstein数字,这是用于量化火焰伸展的适当非倾向参数。对热效应,反应速率敏感性,中间物种分布和反应路径的研究随后证明动力学效应是火焰速度排序的主要原因。具体地,由于S-丁醇,丁醇和叔丁醇都具有支链分子结构,它们裂成相对稳定的支链中间物质,例如异丁烯,异丙肾和丙酮,因此取决于一定程度的火焰速度燃料分子支化。

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