Kulmala Markku, Riipinen Ilona, Sipilä Mikko, Manninen Hanna E, Petäjä Tuukka, Junninen Heikki, Maso Miikka Dal, Mordas Genrik, Mirme Aadu, Vana Marko, Hirsikko Anne, Laakso Lauri, Harrison Roy M, Hanson Ian, Leung Carl, Lehtinen Kari E J, Kerminen Veli-Matti
Department of Physical Sciences, University of Helsinki, Post Office Box 64, FI-00014, Helsinki, Finland.
Science. 2007 Oct 5;318(5847):89-92. doi: 10.1126/science.1144124. Epub 2007 Aug 30.
Atmospheric aerosol formation is known to occur almost all over the world, and the importance of these particles to climate and air quality has been recognized. Although almost all of the processes driving aerosol formation take place below a particle diameter of 3 nanometers, observations cover only larger particles. We introduce an instrumental setup to measure atmospheric concentrations of both neutral and charged nanometer-sized clusters. By applying the instruments in the field, we come to three important conclusions: (i) A pool of numerous neutral clusters in the sub-3 nanometer size range is continuously present; (ii) the processes initiating atmospheric aerosol formation start from particle sizes of approximately 1.5 nanometers; and (iii) neutral nucleation dominates over the ion-induced mechanism, at least in boreal forest conditions.
众所周知,大气气溶胶的形成几乎在世界各地都会发生,并且这些颗粒物对气候和空气质量的重要性已得到认可。尽管几乎所有驱动气溶胶形成的过程都发生在粒径小于3纳米的情况下,但观测仅涵盖较大的颗粒。我们引入了一种仪器装置来测量大气中中性和带电纳米级团簇的浓度。通过在实地应用这些仪器,我们得出了三个重要结论:(i)在亚3纳米尺寸范围内持续存在大量中性团簇;(ii)引发大气气溶胶形成的过程从大约1.5纳米的粒径开始;(iii)至少在北方森林条件下,中性成核比离子诱导机制占主导地位。