510g Adsorption Isotherm of Sodium Dodecyl Sulfate In Hydrate Particles

Jae W. Lee1, Chi Lo2, Junshe Zhang3, Alexander Couzis4, S. Lu5, and Ponisseril Somasundaran5. (1) Department of Chemical Engineering, The City College of New York, 140th street and Convent Ave, New York, NY 10031, (2) Chem Eng Dept, The City College of New York, 140th St and Convent Ave, New York, NY 10031, (3) Chemical Engineering Dept, The City College of New York, 140th St and Convent Ave, New York, NY 10031, (4) Chemical Engineering, City College and the Graduate Center of the City University of New York, Steinman Hall, 140th St @ Convent Ave, New York, NY 10031, (5) Earth and Environmental Eng, Columbia University, Room 911, Mudd Bldg., 500W 120th Street, New York, NY 10027

Sodium dodecyl sulfate (SDS) has been known to accelerate gas hydrate formation. One possible mechanism proposed that SDS forms micelles in bulk water phase and the hydrophobic environment inside the micelles accommodates non-polar guest molecules such as methane, ethane, propane, etc. so the fast nucleation may be induced by having better contact between water and guest molecules [1]. However, recent studies [2-4] reported that SDS does not form micelles if the gas hydrate formation temperature is below the normal Krafft point (281-289 K) for SDS. We proposed [5] that SDS reduces the energy barrier of hydrate nucleation by adsorbing onto hydrate nucleus surface. We will characterize the SDS adsorption onto the CP hydrates using zeta-potential measurements and will present the SDS isotherm with particle size distribution of gas hydrates.

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