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Measured particle water uptake enhanced by co-condensing vapours

机译:通过共聚蒸气增强了测量的颗粒水摄取

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Co-condensation of inorganic or organic vapours on growing droplets could significantly enhance both cloud condensation nucleus (CCN) and cloud droplet number concentration, thereby influencing cloud albedo and climate. Until now, there has been very few direct observational evidence of this process. We have measured the growth of inorganic salt particles exposed to both water and organic vapours at 291.15K in the laboratory, showing that co-condensation of the organic vapours significantly enhances water uptake of aerosols. After exposure to water and propylene glycol vapours, ammonium sulfate particles grew much more than any previously measured particles, inorganic or organic, at the same relative humidity (RH). The maximum equivalent hygroscopicity parameter, κ, was observed to reach up to 2.64, very much higher than values (0.1κ0.9) measured for atmospheric particulate matter using conventional instrumentation, which may be blind to this effect. Under a continuously replenishing organic vapour field, the particles never reached equilibrium owing to the presence of the involatile solute and were observed to continuously grow with increasing exposure time, in agreement with model simulations. Co-condensation of butylene glycol (which has similar volatility but, at aw?=?0.9, a higher Sorg than propylene glycol in our system) and tri-ethylene glycol (which has lower volatility and, at aw?=?0.9, lower Sorg than propylene glycol in our system) vapours was additionally measured in this study. The maximum equivalent hygroscopicity parameter, κ, reached as high as 8.48 for ammonium sulfate particles exposed to water and tri-ethylene glycol vapours at 90% RH. This enhancement of particle water uptake through co-condensation of vapours constitutes the direct measurement of this process, which may substantially influence cloud droplet formation in the atmosphere. In addition, the model simulations for exposure to co-condensing butylene glycol and tri-ethylene glycol vapours with water show that there are factors other than Sorg which influence the co-condensation of semi-volatile organic compounds (SVOCs) that are as yet not understood.
机译:在生长液滴上的无机或有机蒸汽的共聚可以显着增强云凝结核(CCN)和云液滴数浓度,从而影响云反玻璃和气候。到目前为止,这一过程的直接观察证据很少。我们已经测量了在实验室中291.15K暴露于水和有机蒸汽的无机盐颗粒的生长,表明有机蒸汽的共凝聚显着增强了气溶胶的吸水。暴露于水和丙二醇蒸气中后,硫酸铵颗粒在相同的相对湿度(RH)处比任何先前测量的颗粒,无机或有机物增长得多。观察到最大等效的吸湿性参数κ达到高达2.64,非常高于使用常规仪器测量的大气颗粒物测量的值(0.1k0.9),这可能对这种效果视而不见。在连续补充有机蒸气场下,由于存在脱脂溶质的存在,颗粒从未达到平衡,并且观察到与模型模拟一致,随着曝光时间的增加而连续生长。丁二醇的共聚(其具有相似的挥发性,但在AW?= 0.9,比我们的系统中的丙二醇高于丙二醇)和三乙二醇(挥发性较低,在AWα= 0.9,下部在本研究中另外测量了我们系统中的丙二醇的载体。对于暴露于水和三乙二醇蒸汽的硫酸铵颗粒,最高等效的吸湿性参数,κ达到高达8.48,以90%RH暴露于水和三乙二醇蒸汽。这种通过蒸气共缩的颗粒水吸收的增强构成了该方法的直接测量,这可能会在大气中显着影响云液滴形成。此外,用于暴露于共缩丁二醇和三乙二醇蒸气的模型模拟与水的蒸气显示出存在的因素除Sorg以外,影响了半挥发性有机化合物(SVOCs)的共聚缩合了解。

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