Hung Hui-Ming, Ariya Parisa
Department of Atmospheric and Oceanic Sciences, 805 Sherbrooke Street West, Montreal QC H3A 2T5, Canada.
J Phys Chem A. 2007 Feb 1;111(4):620-32. doi: 10.1021/jp0654563.
The heterogeneous reactions of oleic acid (OL) and oleic-acid/sodium-chloride(aq) (OL/NaCl(aq)) mixture droplets with ozone are studied at two relative humidities (RH). The reactions were monitored concomitantly using attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FT-IR) for the organic species and UV-vis spectrometry for the ozone concentration in order to investigate reaction rate discrepancies reported in literature as well as the oxidation mechanism. The less volatile products were identified and resolved by a Fourier transform ion cyclotron resonance mass spectrometer (FT-ICR-MS). This led to identification of 13 organic molecules (up to 45 carbons). Identified products were predominantly composed by nananoic acid and azelaic acid. Our results suggest that the propagation reaction is possibly initiated by a secondary reaction such as the stabilized Criegee intermediates reacting with oleic acid. For hygroscopic properties, the ATR-IR spectra at high RH (87 +/- 5%) showed that the hydrophobic oleic acid droplets can take up water slightly when exposed to ozone. For internally mixed OL/NaCl(aq) droplets, the hygroscopic properties of the droplets upon ozone exposure were found to be complex; hygroscopic properties or the growth factors of the droplets are altered as the oxidation products of oleic acid exist concurrently with NaCl(aq). Furthermore, the concentration of ozone was monitored to examine the kinetics of the oxidation reaction. The integrated ozone profile recorded by UV-vis spectrometry showed the consumed ozone represents only 30 +/- 2% of total oleic acid and hence confirmed the existence of secondary reactions. A kinetic model was used to simulate an ozone temporal profile that could only be described if the secondary reactions were included. The discrepancy of ozone uptake coefficients according to the OL and ozone measurements as well as their atmospheric implications are herein discussed.
在两种相对湿度(RH)条件下,研究了油酸(OL)以及油酸/氯化钠水溶液(OL/NaCl(aq))混合液滴与臭氧的非均相反应。使用衰减全反射傅里叶变换红外光谱(ATR-FT-IR)监测有机物种的反应情况,同时用紫外可见光谱法监测臭氧浓度,以研究文献中报道的反应速率差异以及氧化机制。用傅里叶变换离子回旋共振质谱仪(FT-ICR-MS)对挥发性较小的产物进行鉴定和解析。这使得鉴定出了13种有机分子(碳原子数最多为45个)。鉴定出的产物主要由壬二酸和壬二酸组成。我们的结果表明,传播反应可能是由诸如稳定的Criegee中间体与油酸反应这样的二级反应引发的。对于吸湿性,高相对湿度(87±5%)下的ATR-IR光谱表明,疏水性的油酸液滴在暴露于臭氧时会轻微吸水。对于内部混合的OL/NaCl(aq)液滴,发现臭氧暴露后液滴的吸湿性很复杂;由于油酸的氧化产物与NaCl(aq)同时存在,液滴的吸湿性或生长因子会发生改变。此外,监测臭氧浓度以研究氧化反应的动力学。紫外可见光谱法记录的积分臭氧曲线表明,消耗的臭氧仅占总油酸的30±2%,从而证实了二级反应的存在。使用动力学模型模拟臭氧时间曲线,只有包含二级反应才能描述该曲线。本文讨论了根据OL和臭氧测量得出的臭氧吸收系数差异及其大气影响。