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Organic aerosol growth by acid-catalyzed heterogeneous reactions of octanal in a flow reactor

机译:流动反应器中辛烷的酸催化异相反应使有机气溶胶生长

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摘要

Octanal was chosen as a model carbonyl compound to study aerosol growth by the heterogeneous acid-catalyzed reactions. The heterogeneous reactions of octanal in the presence/absence of acidified seed aerosols were conducted in a 2 m flow reactor (2.5 cm. ID) under darkness in the presence of background seed aerosols. To facilitate hemiacetal/acetal formation via the acid-catalyzed heterogeneous reaction of octanal, 1-nonanol was also co-injected with inorganic seed aerosols into the flow reactor system. The aerosol population was measured from a series of sampling ports down the flow reactor as a function of distance using a scanning mobility particle sizer (SMPS). These results were used to predict the apparent rate constants for heterogeneous reactions of octanal, optimizing experimentally observed aerosol growth from condensation and heterogeneous reactions. The aldehyde heterogeneous reactions were accelerated in the presence of an acid catalyst (H2SO4), and led to higher aerosol yields, than when H2SO4 was not present in the seed aerosol. Our results showed that the log of the organic aerosol yield is inversely related to humidity in the presence of an acid-catalyst (R-2 = 0.98). When aerosols were not catalyzed with an acid, aerosol growth %yields were neither sensitive nor linear with %RH (R-2 = 0.18). These results may be explained by the fact that acid-catalyzed heterogeneous reactions of aldehydes are significantly accelerated as the acidity increases. The SMPS was also operated in two different aerosol-sampling flow rates to characterize particle off-gassing while particles were inside the SMPS. The off-gassing of organic compounds from the particle phase was smaller with an acid catalyst than without an acid catalyst. Fourier transform infrared spectrometry (FTIR) was employed to demonstrate the direct transformation of chemical functional groups by acid-catalyzing the reactions of octanal with 1-nonanol as a thin liquid layer on a zinc selenide (ZnSe) FTIR disk. It was concluded that carbonyls, which are produced by atmospheric photochemical oxidation reactions, can significantly contribute to secondary organic aerosol formation through acid-catalyzed heterogeneous reactions. (C) 2003 Elsevier Science Ltd. All rights reserved. [References: 58]
机译:选择辛酸为模型的羰基化合物,以研究异质酸催化反应中气溶胶的生长。在存在/不存在酸化种子气溶胶的情况下,辛烷的异相反应是在2m流动反应器(2.5厘米内径)中,在黑暗条件下,在有背景种子气溶胶的条件下进行的。为了通过辛酸的酸催化异相反应促进半缩醛/缩醛的形成,还将1-壬醇与无机种子气雾剂共同注入流动反应器系统中。使用扫描迁移率粒度仪(SMPS),从距离流动反应器向下的一系列采样端口测量的气溶胶数量与距离成函数关系。这些结果被用于预测八角形异相反应的表观速率常数,优化了从凝结和异相反应中观察到的气溶胶生长。与在种子气雾剂中不存在H2SO4的情况相比,在酸催化剂(H2SO4)的存在下,醛的异相反应会加速,并导致更高的气雾剂产率。我们的结果表明,在存在酸催化剂(R-2 = 0.98)的情况下,有机气溶胶产量的对数与湿度成反比。当气溶胶不被酸催化时,气溶胶的生长百分率既不敏感也不与线性关系成线性关系(R-2 = 0.18)。这些结果可以通过以下事实来解释:随着酸度的增加,醛的酸催化的异相反应显着加速。 SMPS还以两种不同的气溶胶采样流速运行,以表征颗粒在SMPS内时的除气特性。用酸催化剂的颗粒相中的有机化合物的放气要比不用酸催化剂的小。傅里叶变换红外光谱(FTIR)用于通过酸催化辛酸与1-壬醇(作为硒化锌(ZnSe)FTIR圆盘上的薄液层)的反应,对化学官能团进行直接转化。结论是,大气光化学氧化反应产生的羰基可通过酸催化的异相反应显着促进二次有机气溶胶的形成。 (C)2003 Elsevier ScienceLtd。保留所有权利。 [参考:58]

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