10.6084/m9.figshare.8231150.v2
Caroline Dang
Caroline
Dang
Thomas Bannan
Thomas
Bannan
Petroc Shelley
Petroc
Shelley
Michael Priestley
Michael
Priestley
Stephen D. Worrall
Stephen D.
Worrall
John Waters
John
Waters
Hugh Coe
Hugh
Coe
Carl J. Percival
Carl J.
Percival
David Topping
David
Topping
The effect of structure and isomerism on the vapor pressures of organic molecules and its potential atmospheric relevance
Taylor & Francis Group
2019
isomerism
KEMS
mass spectrometry techniques
vapor pressure values
state vapor pressures
mass loadings show
vapor pressure
use group contribution methods
state vapor pressure
vapor pressures
alkyl chain length
carboxylic acid groups
relevance Knudsen Effusion Mass Spectrometry
molecule
2019-06-24 21:25:44
Journal contribution
https://tandf.figshare.com/articles/journal_contribution/The_effect_of_structure_and_isomerism_on_the_vapour_pressures_of_organic_molecules_and_its_potential_atmospheric_relevance/8231150
<p>Knudsen Effusion Mass Spectrometry (KEMS) was used to find the solid state vapor pressures of a range of atmospherically relevant organic molecules from 298 K to 333 K. The selection of species analyzed allowed for the effect of structural isomerism, specifically positional isomerism, and stereoisomerism, specifically geometric isomerism, on solid state vapor pressure to be investigated. In addition, the effect of varying the number of carboxylic acid groups present within a molecule’s structure and of varying alkyl chain length was assessed. The solid state vapor pressures were converted to subcooled liquid vapor pressures using experimental heat of fusion and melting point values. The resulting subcooled liquid vapor pressures were found to be up to 7 orders of magnitude lower than the vapor pressures estimated from models. Some of this variation between experimentally determined subcooled liquid vapor pressures and predicted vapor pressures, which use group contribution methods, can be attributed to the effects of isomerism which are largely not taken into account in models. Whilst these techniques might have both structural and parametric uncertainties, of the compound classes tested, a general inverse relationship between melting point and solid state vapor pressure was observed. Within each compound class the variations in vapor pressure can be attributed to the number and size of functional groups present and the relative positions of those functional groups to each other both positionally and geometrically. These two factors impact upon both the molecules’ dipole moments and upon their ability to interact both intramolecularly and intermolecularly via hydrogen bonding, thus explaining the differences in observed vapor pressure. Partitioning calculations using a range of condensed mass loadings show that whilst using vapor pressure values derived from models would put most of the compounds in the vapor phase, using the experimental values obtained here would mean a significant fraction of the organic molecules would be in the condensed phase. This could have a significant impact upon the formation and nature of atmospheric aerosol, and comparisons with ambient data obtained from other mass spectrometry techniques during bonfire night in Manchester in 2016 are made in an attempt to assess this potential atmospheric importance.</p>