Abstract
We investigate the phase behavior of an asymmetric binary liquid A-W mixture confined between two planar homogenous substrates (slit pore). Molecules of species W interact preferentially with the solid walls via a long-range potential. Assuming nearest-neighbor attractions between the liquid molecules, we employ a lattice-gas model and a mean-field approximation for the grand potential. Minimization of this potential yields the density profiles of thermodynamically stable phases for fixed temperature, chemical potentials of both species, pore width and strengths of attraction. This model is used to analyze experimental small-angle neutron-scattering (SANS) data on the microscopic structure of the binary system isobutyric acid (iBA)+heavy water (D2 O) inside a mesoscopic porous matrix (controlled-pore glass of about 10 nm mean pore width). Confinement-independent model parameters are adjusted so that the theoretical liquid-liquid coexistence curve in the bulk matches its experimental counterpart. By choosing appropriate values of the pore width and the attraction strength between substrates and water we analyze the effect of confinement on the phase diagram. In addition to a depression of the liquid-liquid critical point we observe surface induced phase transitions as well as water-film adsorption near the walls. The temperature dependence of the structure of water-rich and iBA-rich phases of constant composition are discussed in detail. The theoretical predictions are consistent with results of the SANS study and assist their interpretation.
Original language | English |
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Article number | 124510 |
Journal | Journal of Chemical Physics |
Volume | 122 |
Issue number | 12 |
DOIs | |
State | Published - Mar 22 2005 |
Externally published | Yes |
Funding
This work was supported by the Deutsche Forschungsgemeinschaft in the framework of the Sonderforschungsbereich 448 “Mesoskopisch strukturierte Verbundsysteme.” The SANS measurements 13 were performed at GeNF (GKSS Forschungszentrum Geesthacht).
Funders | Funder number |
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Deutsche Forschungsgemeinschaft |