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Cryogenic Liquid Jets for High Repetition Rate Discovery Science
Published on: May 9, 2020
Argon nucleation in a cryogenic nucleation pulse chamber
Kristina Iland1, Judith Wölk, Reinhard Strey
1Institut für Physikalische Chemie, Universität zu Köln, 50939 Cologne, Germany.
The Journal of Chemical Physics
|October 24, 2007
Summary
Homogeneous nucleation of argon droplets was measured, revealing significant discrepancies with classical nucleation theory. New data show experimental rates are orders of magnitude lower than theoretical predictions.
Area of Science:
- Physical Chemistry
- Thermodynamics
- Materials Science
Background:
- Homogeneous nucleation is a fundamental process in phase transitions.
- Previous studies lacked systematic nucleation onset data for argon.
- Classical nucleation theory (CNT) often overestimates nucleation rates.
Purpose of the Study:
- To present the first systematic nucleation onset data for argon.
- To compare experimental data with predictions from various nucleation theories.
- To determine the size of the critical nucleus for argon droplet formation.
Main Methods:
- Utilized a newly designed cryogenic nucleation pulse chamber.
- Measured nucleation onset data across a temperature range of 42-58 K and vapor pressures of 0.3-10 kPa.
- Employed optical detection and Gibbs-Thomson equation for analysis.
Main Results:
- Experimental nucleation rates differ from CNT by 16-26 orders of magnitude.
- Self-consistent theory (Girshick and Chiu) showed improved temperature dependence but still large discrepancies (11-17 orders of magnitude).
- Thermodynamically consistent theory (Kashchiev) agreed well with temperature dependence, predicting rates 5-7 orders of magnitude below experimental values.
Conclusions:
- Classical and self-consistent nucleation theories significantly overestimate argon nucleation rates.
- The thermodynamically consistent theory provides a better, though still quantitatively different, prediction.
- The critical nucleus for argon contains approximately 40-80 atoms.

