How CO2 gas accelerates water nucleation at low temperature.

IF 3.1 2区 化学 Q3 CHEMISTRY, PHYSICAL Journal of Chemical Physics Pub Date : 2024-11-14 DOI:10.1063/5.0233794
Stefan Feusi, Felix Graber, Jai Khatri, Chenxi Li, Ruth Signorell
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Abstract

We conducted homogeneous nucleation experiments for dilute binary H2O-CO2 mixtures in Ar-N2 carrier gas with different CO2/H2O ratios at temperatures of 57 and 75 K and total pressures of ∼40 and 70 Pa, respectively. Direct experimental information on the number and type of molecules in the clusters and on the cluster number concentration is obtained by mass spectrometric detection of nucleating clusters that form in the uniform region of Laval expansions. Only homo-molecular water clusters are observed in the mass spectra. However, as the CO2/H2O ratio increases, a significant increase in the nucleation rate is observed. A simple kinetic model suggests that this acceleration of nucleation is due to the formation of short-lived, transient hetero-molecular H2O-CO2 dimers. Comparison with homogeneous binary nucleation of toluene-CO2 and unary nucleation of H2O shows that nucleation becomes more efficient in systems with stronger intermolecular interactions and a larger number of degrees of freedom. Such studies at the molecular level will improve our understanding of homogeneous nucleation mechanisms in atmospheric and industrial processes.

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二氧化碳气体如何在低温下加速水的成核。
我们对 Ar-N2 载气中不同 CO2/H2O 比率的稀二元 H2O-CO2 混合物进行了均匀成核实验,实验温度分别为 57 和 75 K,总压力分别为 40 和 70 Pa。通过对在拉瓦尔膨胀均匀区域形成的成核簇进行质谱检测,获得了有关簇中分子数量和类型以及簇数量浓度的直接实验信息。在质谱中只能观察到同分子水簇。然而,随着 CO2/H2O 比率的增加,成核率也会显著增加。一个简单的动力学模型表明,成核加速是由于形成了短寿命、瞬时的异分子 H2O-CO2 二聚体。与甲苯-CO2 的同质二元成核和 H2O 的单元成核比较表明,在分子间相互作用更强、自由度更大的体系中,成核效率更高。这种分子水平的研究将提高我们对大气和工业过程中均相成核机制的理解。
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来源期刊
Journal of Chemical Physics
Journal of Chemical Physics 物理-物理:原子、分子和化学物理
CiteScore
7.40
自引率
15.90%
发文量
1615
审稿时长
2 months
期刊介绍: The Journal of Chemical Physics publishes quantitative and rigorous science of long-lasting value in methods and applications of chemical physics. The Journal also publishes brief Communications of significant new findings, Perspectives on the latest advances in the field, and Special Topic issues. The Journal focuses on innovative research in experimental and theoretical areas of chemical physics, including spectroscopy, dynamics, kinetics, statistical mechanics, and quantum mechanics. In addition, topical areas such as polymers, soft matter, materials, surfaces/interfaces, and systems of biological relevance are of increasing importance. Topical coverage includes: Theoretical Methods and Algorithms Advanced Experimental Techniques Atoms, Molecules, and Clusters Liquids, Glasses, and Crystals Surfaces, Interfaces, and Materials Polymers and Soft Matter Biological Molecules and Networks.
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