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Cloud condensation nuclei droplet growth kinetics of ultrafine particles during anthropogenic nucleation events

机译:人为成核过程中超细颗粒云凝结核滴的生长动力学

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摘要

Evolution of the cloud condensation nucleus (CCN) activity of 36 ±4nm diameter anthropogenic aerosol particles at a water supersaturation of 1.0 ± 0.1% is examined for particle nucleation and growth. During the early stages of one event, relatively few of the anthropogenic particles at 36 nm were CCN active and their growth rates by water condensation were delayed relative to ammonium sulphate particles. As the event progressed, the particle size distribution evolved to larger sizes and the relative numbers of particles at 36 nm that were CCN active increased until all the 36 nm particles were activating at the end of the event. Based on the chemistry of larger particles and the results from an aerosol chemical microphysics box model, the increase in CCN activity of the particles was most likely the result of the condensation of sulphate in this case. Despite the increased CCN activity, a delay was observed in the initial growth of these particles into cloud droplets, which persisted even when the aerosol was most CCN active later in the afternoon. Simulations show that the delay in water uptake is explained by a reduction of the mass accommodation coefficient assuming that the composition of the 36 nm particles is the same as the measured composition of the 60—100 nm particles.
机译:检查了水过饱和度为1.0±0.1%时,直径为36±4nm的人为气溶胶颗粒的云凝结核(CCN)活性的演变,以了解颗粒的成核和生长情况。在一个事件的早期阶段,在36 nm处的人为颗粒相对很少,具有CCN活性,相对于硫酸铵颗粒,它们因水凝结而产生的生长速率被延迟。随着事件的进行,粒度分布逐渐变大,并且具有CCN活性的36 nm粒子的相对数量增加,直到事件结束时所有36 nm粒子都被激活为止。基于较大颗粒的化学性质和气溶胶化学微物理学箱模型的结果,在这种情况下,颗粒CCN活性的增加很可能是硫酸盐缩合的结果。尽管CCN活性增加,但观察到这些颗粒最初形成云滴的时间有所延迟,即使在下午晚些时候气溶胶中CCN的活性最高时,这种影响仍然持续。模拟表明,假设36 nm颗粒的组成与60-100 nm颗粒的测量组成相同,则吸水延迟可通过降低质量调节系数来解释。

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  • 来源
    《Atmospheric environment》 |2012年第2期|p.389-398|共10页
  • 作者单位

    Department of Chemistry, University of Toronto, Toronto, Ontario, Canada;

    Department of Physics and Atmospheric Science, Dalhousie University, Halifax, Nova Scotia, Canada;

    Department of Chemistry, University of Toronto, Toronto, Ontario, Canada;

    Department of Chemistry, University of Toronto, Toronto, Ontario, Canada,Science and Technology Branch, Environment Canada, 4905 Dufferin St., Toronto, ON, M3H 5T4, Canada;

    Department of Chemistry, University of Toronto, Toronto, Ontario, Canada,Institute of Chemical Engineering and High Temperature Processes (ICE-HT), Foundation for Research & Technology, Hellas (FORTH), Patras, Greece;

    Department of Chemistry, University of Toronto, Toronto, Ontario, Canada;

    Department of Chemistry, University of Toronto, Toronto, Ontario, Canada;

    Science and Technology Branch, Environment Canada, 4905 Dufferin St., Toronto, ON, M3H 5T4, Canada;

    Science and Technology Branch, Environment Canada, 4905 Dufferin St., Toronto, ON, M3H 5T4, Canada;

    Department of Chemistry, University of Toronto, Toronto, Ontario, Canada;

    Science and Technology Branch, Environment Canada, 4905 Dufferin St., Toronto, ON, M3H 5T4, Canada;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    aerosols; CCN; water uptake; growth kinetics; nucleation;

    机译:气雾剂CCN;水分吸收生长动力学;成核;

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