Wagner P E, Kaller D, Vrtala A, Lauri A, Kulmala M, Laaksonen A
Institut für Experimentalphysik, Universität Wien, Boltzmanngasse 5, A-1090 Wien, Austria.
Phys Rev E Stat Nonlin Soft Matter Phys. 2003 Feb;67(2 Pt 1):021605. doi: 10.1103/PhysRevE.67.021605. Epub 2003 Feb 24.
Nucleation probabilities for binary heterogeneous nucleation have been measured quantitatively. Heterogeneous nucleation of binary n-propanol-water vapor mixtures on partially soluble 6.9-nm NaCl particles and on nonsoluble oxidized and nonoxidized 8-nm Ag particles at a constant nucleation temperature of 288 K (NaCl) or 285 K (Ag) has been investigated experimentally and theoretically. An expansion chamber was applied to generate supersaturated vapor mixtures. Number concentrations of particles activated to condensational growth were determined optically for various vapor phase activities at constant temperature. Nucleation probabilities have been measured as functions of the vapor phase activities for several n-propanol-water vapor mixing ratios. Beyond certain vapor phase activities a sharp onset of heterogeneous nucleation was observed both for NaCl and for Ag particles. For insoluble particle surfaces the theoretical slopes of the nucleation probability versus vapor phase activity curves were found to be somewhat steeper as compared to the experiment. On the other hand, for soluble particles the experimental slopes were found to be in satisfactory agreement with theory. The onset of the nucleation process is defined at an activity value where 50% of the particles were activated to condensational growth. Onset activities were obtained for various mixing ratios of the binary vapor mixtures. In the case of NaCl nuclei for n-propanol rich mixtures, the heterogeneous nucleation calculations based on a thermodynamically consistent version of Fletcher theory and an experimentally determined contact angle provide a reasonable approximation of the experimental data. However, it appears that the Fletcher theory is not applicable in the region of transition from n-propanol rich to water rich mixtures. Based on the Köhler theory of activation of soluble particles, a theory was formulated accounting for the presence of two condensable vapors and limited solubility of NaCl in water-propanol liquid mixtures. This approach provides a satisfactory description of the transition from activation of soluble particles to nucleation of vapors on insoluble particles. In the case of silver particles Fletcher theory with macroscopic experimental contact angles as well as with contact angle zero results in strong deviations from experimental data. A significant improvement was achieved by introducing fit contact angles, which are substantially lower than the macroscopic experimental values and may be considered as approximate values of the microscopic contact angles.
已对二元异质成核的成核概率进行了定量测量。在288K(NaCl)或285K(Ag)的恒定成核温度下,研究了二元正丙醇 - 水蒸气混合物在部分可溶的6.9纳米NaCl颗粒以及不可溶的氧化和未氧化的8纳米Ag颗粒上的异质成核现象,包括实验研究和理论研究。采用膨胀室来产生过饱和蒸气混合物。在恒温下,通过光学方法测定了各种气相活度下被激活进行凝结生长的颗粒的数浓度。测量了几种正丙醇 - 水蒸气混合比下成核概率与气相活度的函数关系。在超过特定气相活度时,观察到NaCl颗粒和Ag颗粒的异质成核均急剧开始。对于不可溶颗粒表面,发现成核概率与气相活度曲线的理论斜率相比实验值略陡。另一方面,对于可溶颗粒,实验斜率与理论值吻合良好。成核过程的起始定义为50%的颗粒被激活进行凝结生长时的活度值。获得了二元蒸气混合物各种混合比下的起始活度。对于富含正丙醇的混合物中的NaCl核,基于热力学一致的弗莱彻理论版本和实验确定的接触角进行的异质成核计算,能合理地近似实验数据。然而,在从富含正丙醇的混合物过渡到富含水的混合物区域,弗莱彻理论似乎并不适用。基于可溶颗粒活化的克勒理论,提出了一种考虑两种可凝蒸气存在以及NaCl在水 - 丙醇液体混合物中有限溶解度的理论。这种方法能令人满意地描述从可溶颗粒活化到不可溶颗粒上蒸气成核的转变。对于银颗粒,采用宏观实验接触角以及接触角为零的弗莱彻理论与实验数据有很大偏差。通过引入拟合接触角取得了显著改进,拟合接触角远低于宏观实验值,可视为微观接触角的近似值。