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Organic aerosol volatility and viscosity in the North China Plain: contrast between summer and winter

机译:华北平原有机气溶胶波动和粘度:夏季与冬季对比

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Volatility and viscosity have substantial impacts on gas–particle partitioning, formation and evolution of aerosol and hence the predictions of aerosol-related air quality and climate effects. Here aerosol volatility and viscosity at a rural site (Gucheng) and an urban site (Beijing) in the North China Plain (NCP) in summer and winter were investigated by using a thermodenuder coupled with a high-resolution aerosol mass spectrometer. The effective saturation concentration ( C * ) of organic aerosol (OA) in summer was smaller than that in winter (0.55? μ g?m ?3 vs. 0.71–0.75? μ g?m ?3 ), indicating that OA in winter in the NCP is more volatile due to enhanced primary emissions from coal combustion and biomass burning. The volatility distributions varied and were largely different among different OA factors. In particular, we found that hydrocarbon-like OA (HOA) contained more nonvolatile compounds compared to coal-combustion-related OA. The more oxidized oxygenated OA (MO-OOA) showed overall lower volatility than less oxidized OOA (LO-OOA) in both summer and winter, yet the volatility of MO-OOA was found to be relative humidity (RH) dependent showing more volatile properties at higher RH. Our results demonstrated the different composition and chemical formation pathways of MO-OOA under different RH levels. The glass transition temperature ( T g ) and viscosity of OA in summer and winter are estimated using the recently developed parameterization formula. Our results showed that the T g of OA in summer in Beijing (291.5?K) was higher than that in winter (289.7–290.0?K), while it varied greatly among different OA factors. The viscosity suggested that OA existed mainly as solid in winter in Beijing (RH? = ?29? ± ?17?%), but as semisolids in Beijing in summer (RH? = ?48? ± ?25?%) and Gucheng in winter (RH? = ?68? ± ?24?%). These results have the important implication that kinetically limited gas–particle partitioning may need to be considered when simulating secondary OA formation in the NCP.
机译:挥发性和粘度对气溶胶的气体颗粒分配,形成和演化具有显着影响,因此对气溶胶相关的空气质量和气候效应的预测。这里通过使用与高分辨率气溶胶质谱仪相结合的夏季和冬季农村遗址(古城)和冬季城市网站(北京)的气溶胶波动和粘度(北京)。夏季有机气溶胶(OA)的有效饱和浓度(C *)小于冬季(0.55Ωμg≤m≤3vs.0.71-0.75Ωm≤3),表明冬季OA在NCP中,由于煤燃烧和生物质燃烧的初级排放,更具挥发性。波动性分布在不同的OA因子之间变化并且在很大程度上不同。特别是,与煤燃烧相关的OA相比,我们发现烃状OA(HOA)含有更多的非挥发性化合物。夏季和冬季的氧化含氧OA(Mo-OOA)越低挥发性挥发性较低,但发现Mo-OOA的挥发性是相对湿度(RH)依赖性显示出更多的挥发性特性在更高的RH。我们的结果证明了在不同RH水平下MO-OOA的不同组成和化学形成途径。使用最近开发的参数化公式估算夏季和冬季玻璃化转变温度(T g)和粘度。我们的研究结果表明,北京夏季(291.5'K)的oa oa(291.5?k)高于冬季(289.7-290.0.0?k),而在不同的OA因素中可能变化大大变化。粘度表明,OA在北京(RH?=?29?29?±17?17?17?%),但夏季(Rh?= 48?48?25?25?25?25?25?25?25?25?25?25?25?25?25?25?25?25?25?25?25?25?25?25?25?%)和古城的半醇冬天(RH?=?68?±24?%)。这些结果具有重要的意义,即在模拟NCP中模拟次级OA形成时可能需要考虑动力学限制的气体颗粒分配。

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