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• W1964196502 startingPage "1935" @default.
• W1964196502 abstract "Molecular dynamics simulations using a modified Drieding 2.21 force field were carried out to study the coalescence behavior of nanometer-sized water droplets in vacuum and in n-heptane. The coalescence mechanisms of the water droplets in the above-noted environments are fairly similar in a sense that the water droplets form a bridge linking the droplets before they merge. However, in the latter situation, due to the presence of n-heptane molecules in between the water droplets, the coalescence was observed to be slowed down considerably, especially in the first 10 ps of the process. However, once the bridge is formed, the water droplets, in both situations, spend about the same amount of time to form a single droplet. The maximum distance between the droplets above which coalescence does not occur was found to be 10 Å. In terms of the dynamics, the diffusion coefficient of n-heptane in the emulsion system was very close to its value in the pure liquid form. This may be because n-heptane is the continuous phase. Nonetheless, the dynamic behavior of water in n-heptane is different from that of pure water during and after the coalescence. In particular, the self-diffusion coefficient of water molecules in n-heptane is about 20% higher than the experimental value of pure water. Due to the lack of strong attraction forces between water and n-heptane molecules, the n-heptane molecules were observed to orient themselves perpendicularly to the water/n-heptane interfaces so that the contacting area is minimized." @default.
• W1964196502 created "2016-06-24" @default.
• W1964196502 creator A5039073467 @default.
• W1964196502 creator A5058757443 @default.
• W1964196502 date "2004-01-22" @default.
• W1964196502 modified "2023-10-14" @default.
• W1964196502 title "Molecular dynamics simulation of the coalescence of nanometer-sized water droplets in <i>n</i>-heptane" @default.
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• W1964196502 doi "https://doi.org/10.1063/1.1635804" @default.
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