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Water uptake of clay and desert dust aerosol particles at sub- and supersaturated water vapor conditions

机译:在亚饱和和过饱和水蒸气条件下吸收粘土和沙漠尘埃气溶胶颗粒的水

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Airborne mineral dust particles serve as cloud condensation nuclei (CCN), thereby influencing the formation and properties of warm clouds. It is therefore of atmospheric interest how dust aerosols with different mineralogy behave when exposed to high relative humidity (RH) or supersaturation (SS) with respect to liquid water. In this study the subsaturated hygroscopic growth and the supersaturated cloud condensation nucleus activity of pure clays and real desert dust aerosols were determined using a hygroscopicity tandem differential mobility analyzer (HTDMA) and a cloud condensation nuclei counter (CCNC), respectively. Five different illite, montmorillonite and kaolinite clay samples as well as three desert dust samples (Saharan dust (SD), Chinese dust (CD) and Arizona test dust (ATD)) were investigated. Aerosols were generated both with a wet and a dry disperser. The water uptake was parameterized via the hygroscopicity parameter κ. The hygroscopicity of dry generated dust aerosols was found to be negligible when compared to processed atmospheric aerosols, with CCNC derived κ values between 0.00 and 0.02 (the latter corresponds to a particle consisting of 96.7% by volume insoluble material and ~3.3% ammonium sulfate). Pure clay aerosols were generally found to be less hygroscopic than natural desert dust particles. The illite and montmorillonite samples had κ ~ 0.003. The kaolinite samples were less hygroscopic and had κ = 0.001. SD (κ = 0.023) was found to be the most hygroscopic dry-generated desert dust followed by CD (κ = 0.007) and ATD (κ = 0.003). Wet-generated dust showed an increased water uptake when compared to dry-generated samples. This is considered to be an artifact introduced by redistribution of soluble material between the particles. Thus, the generation method is critically important when presenting such data. These results indicate any atmospheric processing of a fresh mineral dust particle which leads'to the addition of more than ~3% soluble material will significantly enhance its hygroscopicity and CCN activity.
机译:空气中的矿物尘埃颗粒充当云凝结核(CCN),从而影响暖云的形成和性质。因此,当暴露于相对于液态水的高相对湿度(RH)或过饱和度(SS)时,具有不同矿物学特征的粉尘气溶胶的行为在大气中引起了人们的关注。在这项研究中,分别使用吸湿性串联差动迁移率分析仪(HTDMA)和云凝结核计数器(CCNC)确定了纯黏土和真实沙漠粉尘气溶胶的亚饱和吸湿性增长和过饱和云凝结核活性。调查了五个不同的伊利石,蒙脱土和高岭石粘土样品,以及三个沙漠尘埃样品(撒哈拉尘埃(SD),中国尘埃(CD)和亚利桑那尘埃(ATD))。湿分散剂和干分散剂均产生气溶胶。通过吸湿性参数κ对吸水率进行参数化。与经处理的大气气溶胶相比,干燥产生的粉尘气溶胶的吸湿性可以忽略不计,CCNC得出的κ值介于0.00和0.02之间(后者对应于由96.7%体积不溶物和〜3.3%硫酸铵组成的颗粒) 。通常发现,纯粘土气溶胶的吸湿性低于天然沙漠尘埃颗粒。伊利石和蒙脱石样品的κ〜0.003。高岭石样品吸湿性较低,κ= 0.001。发现SD(κ= 0.023)是最易吸湿的干燥产生的沙漠尘,其次是CD(κ= 0.007)和ATD(κ= 0.003)。与干产生的样品相比,湿产生的灰尘显示出更高的吸水率。这被认为是由于可溶性材料在颗粒之间的重新分布而引入的假象。因此,在呈现此类数据时,生成方法至关重要。这些结果表明对新鲜矿物粉尘颗粒进行任何大气处理都会导致添加约3%以上的可溶性物质,这将显着提高其吸湿性和CCN活性。

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