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  • 1
    Publication Date: 2015-08-29
    Description: We study the dynamics of two pinned droplets under the influence of an applied electric stress. We find that at a sufficiently strong field, this stress is sufficient to induce contact of the droplets. Interestingly, upon such contact, the dynamic behavior sensitively depends on the separation distance between the droplets. Besides the classical “coalescence” regime, we identify two other dynamic regimes: “fuse-and-split” and “periodic non-coalescence.” In the “fuse-and-split” regime, the droplets first fuse to form a jet, which subsequently breaks up into two droplets. In the “periodic non-coalescence” regime, the droplets contact and bounce away periodically without coalescence. Further analysis indicates that while the electric stress stretches the droplets into shapes that depend on the initial droplet separation, the surface tension stress dominates over the electric stress as soon as the droplets touch. We show that the shapes of the contacting droplets determine their subsequent dynamics. Our work provides a rationale for understanding the interplay between surface tension and electric stresses that govern the behavior of charged droplets and could inspire new methods for characterizing emulsion stability and surfactant performance.
    Print ISSN: 1070-6631
    Electronic ISSN: 1089-7666
    Topics: Physics
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 9280-9286 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The electronic absorption spectra of mono-hydrogenated carbon chain anions C2nH− (n=5–10) have been measured in the gas-phase and in 6 K neon matrices (n=8–12). The techniques of resonant two-color electron photodetachment in the gas-phase and absorption spectroscopy of mass-selected anions in neon matrix were used. A homologous series is observed, with band system origins shifting from 304 nm for C10H− to 590 nm for C20H−. In conjunction with ab initio calculations the band systems are attributed to a 1Σ+←X 1Σ+ transition of linear acetylenic anions. Another near lying electronic transition due to a second isomer is also apparent for C10H− up to C24H−. Comparison with tables of the known diffuse interstellar bands indicates possible matches for the origin bands of the C18H− and C20H− isomers. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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