首页> 外文期刊>Physical chemistry chemical physics: PCCP >Product distributions form the OH radical-induced oxidation of but-1-ene, methyl-substituted but-1-enes and isoprene in NO_x-free air
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Product distributions form the OH radical-induced oxidation of but-1-ene, methyl-substituted but-1-enes and isoprene in NO_x-free air

机译:产物分布形成了在无NO_x的空气中OH自由基引起的丁-1-烯,甲基取代的丁-1-烯和异戊二烯的氧化

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Product distributions resulting from the OH-induced oxidation of but-1ene, 2-methylbut-1-ene, 3-methylbut-1-ene and isoprene in air were measured i nthe absence of nitrogen oxides and compared with predictions based on currently accepted oxidation mechanisms. In the case of butenes, the observed distributios of carbonyl compounds, hydroxyketones, hydroxyalkanals and diols were evaluated to obtain probatilities for the initial attack of OH radical on the outer position of the double bond(#gamma#=0.90+-0.03 for 2-Me-but-1-ene and #gamma#-0.76+-0.05 for both but-1ene and 3-Me-but-1-ene), for the probability of formation of stable products in the self-reaction of secondary #beta#-hydroxyperoxyl radicals (K_(ssb)/K_(SS)=0.29+-0.07 for but-1-ene and K_(ssb)/K_(ss)=0.19+-0.06 for 3-Me-but-1-ene), and for the ratio of the reaction with oxygen vs. decomposition of #beta#-hydroxyalkoxyl radicals, K_3[O_2]/(K_4 + k_3[O_2])= 0.25+-0.04 for but-1-ene and = 0.38 +- 0.04 for 3-Me-but-1-ene. The last two values disagree with other published data, which suggest a smaller effet of oxygen. The oxidation of isoprene produced methacrolein and methyl vinyl ketone with a ratio 0.93+-0.10, the ratio of methyl vinyl ketone and 3-methylfuran was 7.3+-1.0. Other products were 1-hydroxy-3-methylbut-3-n-2-one distribution was complex and could not be fully elucidated. Computer simulations based on several mechanisms applied the relative probabilities for OH addition found fro the but-1-enes. Comparison with the experimental data suggests probabilities for OH additon to the methylated double bond of 0.504+-0.027 (outer position) and 0.056+-0.003(inner position), and to the non-methylated double bond of 0.335+-0.023 (outer position) and 0.015+--0.008(inner position)
机译:在没有氮氧化物的情况下测量了空气中OH诱导的丁烯(1-丁烯,2-甲基丁-1-烯,3-甲基丁-1-烯和异戊二烯)氧化产生的产物分布,并将其与基于当前公认的氧化的预测值进行了比较机制。在丁烯的情况下,评估观察到的羰基化合物,羟基酮,羟基链烷醛和二醇的分布,以获得OH自由基对双键外部位置的初始攻击的能力(对于2-,#gamma#= 0.90 + -0.03 Me-but-1-ene和#gamma#-0.76 + -0.05(对于but-1ene和3-Me-but-1-ene而言),用于在次要#beta的自反应中形成稳定产物的可能性#-羟基过氧自由基(对于丁-1-烯,K_(ssb)/ K_(SS)= 0.29 + -0.07;对于3-Me-丁-1-烯,K_(ssb)/ K_(ss)= 0.19 + -0.06 ),并且对于与氧反应的比率与#beta#-羟基烷氧基自由基分解的比率,丁1烯的K_3 [O_2] /(K_4 + k_3 [O_2])= 0.25 + -0.04和= 0.38 + -3-Me-but-1-ene为0.04。最后两个值与其他已发表的数据不一致,这表明氧气的释放量较小。异戊二烯的氧化产生的甲基丙烯醛和甲基乙烯基酮的比例为0.93 + -0.10,甲基乙烯基酮和3-甲基呋喃的比例为7.3 + -1.0。其他产物为1-羟基-3-甲基丁-3-n-2-one分布较复杂,无法完全阐明。基于几种机制的计算机模拟应用了从丁-1-烯发现OH的相对概率。与实验数据的比较表明,OH加成有0.504 + -0.027(外部)和0.056 + -0.003(内部)的甲基化双键以及0.335 + -0.023(外部位置)的非甲基化双键的可能性。 )和0.015 +-0.008(内部位置)

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