| The Properties of Small Water Clusters from Isothermal Nucleation Rate Measurements | ||
| Barbara E. Wyslouzil1, Yoojeong Kim2, Gerald Wilemski3, Judith Wölk4 and Reinhard Strey4, (1)Chemical and Biomolecular Engineering, The Ohio State University, 140 W 19th Avenue, Columbus, OH 43210, (2)Chemical Engineering, Worcester Polytechnic Institute, 100 Institute Road, Worcester, MA 01609, (3)Physics, University of Missouri - Rolla, Rolla, MO 65409, (4)Institut für Physikalische Chemie, Universität zu Köln, 116 Luxemburgerstrasse, Köln, Germany We have made direct measurements of the stationary, homogeneous nucleation rates, J=N/Δt, in supersonic Laval nozzles. The number densities, N, of droplets formed are measured using small angle neutron scattering (SANS) experiments and the time intervals during which nucleation occurs, Δt <10 μs, are derived from static pressure measurements along the axis of the nozzle. By using nozzles with different expansion rates, we obtain the first isothermal nucleation rate measurements as a function of supersaturation for these devices with a relatively small error margin in J of +/-50%. At temperatures T of 210, 220, and 230 K, the maximum nucleation rates for D2O range between 4•1016< J /cm-3s-1 < 3•1017 for supersaturations S ranging from 46 to 143. Applying the first and second nucleation theorems to isothermal nucleation rate data directly yields estimates for the number of molecules in the critical cluster n* and the excess internal energy Ex(n*), respectively. The agreement between these values and the classical values predicted assuming the critical cluster is a compact spherical object are really quite good even though under our conditions n* is less than 10 and the water is highly supercooled. Extended Abstract Status: Not Uploaded | ||