The dynamics of evaporation from a liquid surface

We explore the collisional energy transfer dynamics of benzene molecules spontaneously evaporating from an in vacuo water -ethanol liquid beam. We find that rotations are cooled significantly more than the lowest-energy vibrational modes, while the rotational energy distributions are Boltzmann. With...

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Main Authors: Maselli, O, Gascooke, J., Lawrance, W., Buntine, Mark
Format: Journal Article
Published: Elsevier 2011
Online Access:http://hdl.handle.net/20.500.11937/25892
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author Maselli, O
Gascooke, J.
Lawrance, W.
Buntine, Mark
author_facet Maselli, O
Gascooke, J.
Lawrance, W.
Buntine, Mark
author_sort Maselli, O
building Curtin Institutional Repository
collection Online Access
description We explore the collisional energy transfer dynamics of benzene molecules spontaneously evaporating from an in vacuo water -ethanol liquid beam. We find that rotations are cooled significantly more than the lowest-energy vibrational modes, while the rotational energy distributions are Boltzmann. Within experimental uncertainty, the rotational temperatures of vibrationally-excited evaporating molecules are the same as the ground state. Collision-induced gas phase energy transfer measurements reveal that benzene undergoes fast rotational relaxation, from which we deduce that the rotational temperature measured in the evaporation experiments (200-230 K) is an indication of the translational energy of the evaporate. Conversely, vibrational relaxation of the high frequency mode, m6, is very inefficient, suggesting that the m6 temperature (260-270 K) is an indication of the liquid surface temperature. Modelling of the relaxation dynamics by both 'temperature gap' and 'Master Equation' approaches indicates that the equivalent of 150-260 hard-sphere collisions occur during the transition from liquid to vacuum.
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institution Curtin University Malaysia
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publishDate 2011
publisher Elsevier
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spelling curtin-20.500.11937-258922017-09-13T15:55:38Z The dynamics of evaporation from a liquid surface Maselli, O Gascooke, J. Lawrance, W. Buntine, Mark We explore the collisional energy transfer dynamics of benzene molecules spontaneously evaporating from an in vacuo water -ethanol liquid beam. We find that rotations are cooled significantly more than the lowest-energy vibrational modes, while the rotational energy distributions are Boltzmann. Within experimental uncertainty, the rotational temperatures of vibrationally-excited evaporating molecules are the same as the ground state. Collision-induced gas phase energy transfer measurements reveal that benzene undergoes fast rotational relaxation, from which we deduce that the rotational temperature measured in the evaporation experiments (200-230 K) is an indication of the translational energy of the evaporate. Conversely, vibrational relaxation of the high frequency mode, m6, is very inefficient, suggesting that the m6 temperature (260-270 K) is an indication of the liquid surface temperature. Modelling of the relaxation dynamics by both 'temperature gap' and 'Master Equation' approaches indicates that the equivalent of 150-260 hard-sphere collisions occur during the transition from liquid to vacuum. 2011 Journal Article http://hdl.handle.net/20.500.11937/25892 10.1016/j.cplett.2011.06.010 Elsevier restricted
spellingShingle Maselli, O
Gascooke, J.
Lawrance, W.
Buntine, Mark
The dynamics of evaporation from a liquid surface
title The dynamics of evaporation from a liquid surface
title_full The dynamics of evaporation from a liquid surface
title_fullStr The dynamics of evaporation from a liquid surface
title_full_unstemmed The dynamics of evaporation from a liquid surface
title_short The dynamics of evaporation from a liquid surface
title_sort dynamics of evaporation from a liquid surface
url http://hdl.handle.net/20.500.11937/25892