Institute for Atmospheric and Earth System Research/Physics, Faculty of Science, University of Helsinki, 00014 Helsinki, Finland.
Center for Atmospheric Particle Studies, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Science. 2021 Feb 5;371(6529):589-595. doi: 10.1126/science.abe0298. Epub 2021 Feb 4.
Iodic acid (HIO) is known to form aerosol particles in coastal marine regions, but predicted nucleation and growth rates are lacking. Using the CERN CLOUD (Cosmics Leaving Outdoor Droplets) chamber, we find that the nucleation rates of HIO particles are rapid, even exceeding sulfuric acid-ammonia rates under similar conditions. We also find that ion-induced nucleation involves IO and the sequential addition of HIO and that it proceeds at the kinetic limit below +10°C. In contrast, neutral nucleation involves the repeated sequential addition of iodous acid (HIO) followed by HIO, showing that HIO plays a key stabilizing role. Freshly formed particles are composed almost entirely of HIO, which drives rapid particle growth at the kinetic limit. Our measurements indicate that iodine oxoacid particle formation can compete with sulfuric acid in pristine regions of the atmosphere.
碘酸(HIO)已知在沿海海洋地区形成气溶胶颗粒,但缺乏预测的成核和生长速率。使用 CERN CLOUD(宇宙离开室外液滴)室,我们发现 HIO 颗粒的成核速率很快,即使在类似条件下也超过了硫酸-氨的速率。我们还发现,离子诱导成核涉及 IO ,并且 HIO 的顺序添加,并且它在+10°C 以下的动力学极限处进行。相比之下,中性成核涉及碘酸(HIO)的反复顺序添加,然后是 HIO,表明 HIO 起着关键的稳定作用。新形成的颗粒几乎完全由 HIO 组成,这在动力学极限下驱动快速的颗粒生长。我们的测量表明,碘氧酸颗粒的形成可以与大气原始区域中的硫酸竞争。