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Grant: Discovery Grants Program - Individual

University of British Columbia

$124,000.00

Phase state and diffusion within atmospheric particles

EF 2017-18

Résumé
Biological sources (for example vegetation) and anthropogenic sources (for example transportation) emit copious quantities of volatile organic compounds. In the atmosphere, these volatile organic compounds are oxidized by a complex series of reactions to form semivolatile organic compounds, followed by condensation of the low volatility products and formation of microscopic particles. We refer to these microscopic particles as secondary organic material (SOM) particles. The term secondary indicates the material is formed in the atmosphere rather than emitted directly into the atmosphere. SOM particles can affect Earths climate by scattering and absorbing solar radiation and by acting as seeds (i.e. nuclei) for clouds. SOM particles can also negatively affect air quality and human health. Currently the scientific understanding of SOM particles is low, which limits our ability to predict their impact on climate, air quality and health. Recent studies have shown that predictions of the mass, size, reactivity, optical properties and cloud nucleating properties of SOM particles are sensitive to the following properties: 1) molecular diffusion of organics within SOM particles, 2) glass formation within SOM particles and 3) liquid-liquid phase separation within SOM particles. This proposal focuses on these three key properties. We will directly measure molecular diffusion rates of organics within SOM particles. The results will be used to quantify the accuracy of the Stokes-Einstein equation, which is often used to estimate diffusion rates of organics in SOM particles. In addition, we will carry out the first direct measurements of diffusion rates of organics within SOM at temperatures less than 293 K, a temperature range relevant to a large part of the atmosphere. We will also determine conditions at which individual SOM particles in the atmosphere become a glass (the same physical state as a glass window pane). Finally, we will determine conditions at which SOM particles undergo liquid-liquid phase separation to form two liquids (a water-rich liquid and an organic-rich liquid) within individual particles. We expect these results will be used by others when predicting the mass, size, reactivity, optical properties and cloud nucleating properties of SOM particles in the atmosphere. In short, these results will be important to many future modelling studies of atmospheric chemistry and climate.
Programme
Discovery Grants Program - Individual
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
RGPIN-2017-04441
Name nom
Bertram, Allan
Department département
Chemistry - Chemistry
Organization id
2
Institution établissement
University of British Columbia
Province en
British Columbia
Province fr
Colombie-Britannique
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2017
Competition year année de concours
2017
Award amount
124000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1504
Committee name en
Chemistry
Committee name fr
Chimie
Area of application code
401
Area of application group en
Environment
Area of application group fr
Environnement
Area of application en
Climate and atmosphere
Area of application fr
Climat et atmosphère
Research subject code
4405
Research subject group en
Atmospheric science
Research subject group fr
Étude de l'atmosphère
Research subject en
Atmospheric chemistry (including air pollution)
Research subject fr
Chimie atmosphérique (y compris pollution atmosphérique)
Partie
1
Nb partie
5
Application title
Phase state and diffusion within atmospheric particles
Keyword
NSERC
Application summary
Biological sources (for example vegetation) and anthropogenic sources (for example transportation) emit copious quantities of volatile organic compounds. In the atmosphere, these volatile organic compounds are oxidized by a complex series of reactions to form semivolatile organic compounds, followed by condensation of the low volatility products and formation of microscopic particles. We refer to these microscopic particles as secondary organic material (SOM) particles. The term secondary indicates the material is formed in the atmosphere rather than emitted directly into the atmosphere. SOM particles can affect Earths climate by scattering and absorbing solar radiation and by acting as seeds (i.e. nuclei) for clouds. SOM particles can also negatively affect air quality and human health. Currently the scientific understanding of SOM particles is low, which limits our ability to predict their impact on climate, air quality and health. Recent studies have shown that predictions of the mass, size, reactivity, optical properties and cloud nucleating properties of SOM particles are sensitive to the following properties: 1) molecular diffusion of organics within SOM particles, 2) glass formation within SOM particles and 3) liquid-liquid phase separation within SOM particles. This proposal focuses on these three key properties. We will directly measure molecular diffusion rates of organics within SOM particles. The results will be used to quantify the accuracy of the Stokes-Einstein equation, which is often used to estimate diffusion rates of organics in SOM particles. In addition, we will carry out the first direct measurements of diffusion rates of organics within SOM at temperatures less than 293 K, a temperature range relevant to a large part of the atmosphere. We will also determine conditions at which individual SOM particles in the atmosphere become a glass (the same physical state as a glass window pane). Finally, we will determine conditions at which SOM particles undergo liquid-liquid phase separation to form two liquids (a water-rich liquid and an organic-rich liquid) within individual particles. We expect these results will be used by others when predicting the mass, size, reactivity, optical properties and cloud nucleating properties of SOM particles in the atmosphere. In short, these results will be important to many future modelling studies of atmospheric chemistry and climate.