Issue 13, 2011

Monomer, clusters, liquid: an integrated spectroscopic study of methanol condensation

Abstract

We have combined static pressure, spectroscopic temperature, Fourier transform infrared spectroscopy (FTIR), and small angle X-ray scattering (SAXS) measurements to develop a detailed picture of methanol condensing from a dilute vapor–carrier gas mixture under the highly supersaturated conditions present in a supersonic nozzle. In our experiments, methanol condensation can be divided into three stages as the gas mixture expands in the nozzle. In the first stage, as the temperature decreases rapidly, small methanoln-mers (clusters) form, increase in concentration, and evolve in size. In the second stage, the temperature decreases more slowly, and the n-mer concentrations continue to rise. Thermodynamic and FTIR experiments cannot, however, definitively establish if the average cluster size is constant or if it continues to increase. Finally, when the vapor becomes supersaturated enough, liquid droplets form via nucleation and growth, consuming more monomer and reducing the concentration of clusters. At the point where liquid first appears, cluster formation has already consumed up to 30% of the monomer. This is significantly more than is predicted by a model that describes the vapor phase as an equilibrium mixture of methanol monomer, dimer, and tetramer. An energy balance suggests that a significant fraction of the cluster population is larger than the tetramer, while preliminary SAXS measurements suggest that these clusters contain, on average, 6 monomers.

Graphical abstract: Monomer, clusters, liquid: an integrated spectroscopic study of methanol condensation

Supplementary files

Article information

Article type
Paper
Submitted
10 Nov 2010
Accepted
14 Jan 2011
First published
18 Feb 2011

Phys. Chem. Chem. Phys., 2011,13, 5855-5871

Monomer, clusters, liquid: an integrated spectroscopic study of methanol condensation

H. Laksmono, S. Tanimura, H. C. Allen, G. Wilemski, M. S. Zahniser, J. H. Shorter, D. D. Nelson, J. B. McManus and B. E. Wyslouzil, Phys. Chem. Chem. Phys., 2011, 13, 5855 DOI: 10.1039/C0CP02485F

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