How do gas hydrates spread on a substrate?

International audience Growth of gas hydrates as fast-growing polycrystalline crusts at interfaces between water and guest phases is well documented, but the mechanisms of hydrate growth on solid substrates are much less known. We report here on cyclopentane (CP) hydrate spreading on glass (fused si...

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Bibliographic Details
Published in:Crystal Growth & Design
Main Authors: de Banos, M.L.M., Hobeika, N., Bouriat, Patrick, Broseta, Daniel, Enciso, E., Clement, Franck, Brown, Ross
Other Authors: Laboratoire des Fluides Complexes et leurs Réservoirs (LFCR), TOTAL FINA ELF-Université de Pau et des Pays de l'Adour (UPPA)-Centre National de la Recherche Scientifique (CNRS), Institut des sciences analytiques et de physico-chimie pour l'environnement et les materiaux (IPREM), Université de Pau et des Pays de l'Adour (UPPA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)
Format: Article in Journal/Newspaper
Language:English
Published: HAL CCSD 2016
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Online Access:https://hal.science/hal-01498748
https://doi.org/10.1021/acs.cgd.6b00471
Description
Summary:International audience Growth of gas hydrates as fast-growing polycrystalline crusts at interfaces between water and guest phases is well documented, but the mechanisms of hydrate growth on solid substrates are much less known. We report here on cyclopentane (CP) hydrate spreading on glass (fused silica) under CP. As seen for methane hydrate by Beltrán and Servio (Cryst. Growth Des. 2010, 10, 4339-4347), CP hydrate grows on glass as a "halo" radiating from the contact line of a "primary" drop. Complementary optical microscopies at micron resolution here allow identification of the mechanisms of halo growth and melting. We conclude that forms of water on the substrate control halo spreading, namely, a precursor film near the contact line and a breath figure (dew) condensed from the CP (halo spreading at ≤2 μm s-1 at T 0 °C or subcooling ∼7 °C), and "leap-frogging" (at ∼10 μm s-1) over "secondary" drops left behind by melting a previous halo. Halo thickening, about 5 nm s-1, is attributed to water condensation, either incorporation of water dissolved in CP (like ablimation) or settling of water "fog" from the CP. Halos spread slower on untreated, compared to hydrophilic, glass, an effect attributed to the quantity of water present on the substrate; a similar trend is noted when the CP phase is not pre-equilibrated with water prior to the experiment. No hydrate halo was detected on hydrophobized (silane-treated) glass, where the breath figure is absent.