The role of low-volatility organic compounds in initial particle growth in the atmosphere
By J. Tröstl, W. Chuang, H. Gordon, M. Heinritzi, Chao Yan, U. Molteni, L. Ahlm, C. Frege, Richard H. Wagner, M. Simon and 59 more. Nature, 2016
708 citations recorded by the source corpus.
About half of present-day cloud condensation nuclei originate from atmospheric nucleation, frequently appearing as a burst of new particles near midday. Atmospheric observations show that the growth rate of new particles often accelerates when the diameter of the particles is between one and ten nanometres. In this critical size range, new particles are most likely to be lost by coagulation with pre-existing particles, thereby failing to form new cloud condensation nuclei that are typically 50 to 100 nanometres across. Sulfuric acid vapour is often involved in nucleation but is too scarce to explain most subsequent growth, leaving organic vapours as the most plausible alternative, at least in the planetary boundary layer. Although recent studies predict that low-volatility organic vapours contribute during initial growth, direct evidence has been lacking. The accelerating growth may result from increased photolytic production of condensable organic species in the afternoon, and the presence of a possible Kelvin (curvature) effect, which inhibits organic vapour condensation on the smallest particles (the nano-Köhler theory), has so far remained ambiguous. Here we present experiments performed in a large chamber under atmospheric conditions that investigate the role of organic vapours in the initial growth of nucleated organic particles in the absence of inorganic acids and bases such as sulfuric acid or ammonia and amines, respectively. Using data from the same set of experiments, it has been shown that organic vapours alone can drive nucleation. We focus on the growth of nucleated particles and find that the organic vapours that drive initial growth have extremely low volatilities (saturation concentration less than 10−4.5 micrograms per cubic metre). As the particles increase in size and the Kelvin barrier falls, subsequent growth is primarily due to more abundant organic vapours of slightly higher volatility (saturation concentrations of 10−4.5 to 10−0.5 micrograms per cubic metre). We present a particle growth model that quantitatively reproduces our measurements. Furthermore, we implement a parameterization of the first steps of growth in a global aerosol model and find that concentrations of atmospheric cloud concentration nuclei can change substantially in response, that is, by up to 50 per cent in comparison with previously assumed growth rate parameterizations.
Subfields: Atmospheric Science, Global and Planetary Change
View Paper: https://www.semanticscholar.org/paper/9dd4aa3e15380db17358c957cebf4736246b07ed
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Atmospheric Science
- Tuukka Petäjä
- Markku Kulmala
- V. Kerminen
- Xuemeng Chen
- Ville Vakkari
- K. Carslaw
- J. Kirkby
- Richard H. Wagner
In Global and Planetary Change
- Tuukka Petäjä
- V. Kerminen
- Markku Kulmala
- Xuemeng Chen
- Ville Vakkari
- J. Kirkby
- K. Carslaw
- Richard H. Wagner
Citations in the corpus
- Atmospheric new particle formation and growth: review of field observations (2018, background): “Likewise, it has been shown that the growth of atmospheric aerosol particles is affected not only by the least volatile compounds, but also by low- and semi-volatile compounds (e.g. Tröstl et al 2016).”
- JournalofGeophysicalResearch : Atmospheres Causes and importance of new particle formation in the present-day and preindustrial atmospheres (2017, positive): “The ionization rates from cosmic rays are calculated from lookup tables [Usoskin et al., 2005, 2011] which are provided for solar cycles from 1952 to 2009, so the effect of the Sun’s magnetic field can be incorporated via the heliospheric modulation potential. The technique of Fraser-Smith [1987] is”