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Molecular segregation observed in a concentrated alcohol–water solution

Abstract

When a simple alcohol such as methanol or ethanol is mixed with water1,2, the entropy of the system increases far less than expected for an ideal solution of randomly mixed molecules3. This well-known effect has been attributed to hydrophobic headgroups creating ice-like or clathrate-like structures in the surrounding water4, although experimental support for this hypothesis is scarce5,6,7. In fact, an increasing amount of experimental and theoretical work suggests that the hydrophobic headgroups of alcohol molecules in aqueous solution cluster together2,8,9,10. However, a consistent description of the details of this self-association is lacking11,12,13. Here we use neutron diffraction with isotope substitution to probe the molecular-scale structure of a concentrated alcohol–water mixture (7:3 molar ratio). Our data indicate that most of the water molecules exist as small hydrogen-bonded strings and clusters in a ‘fluid’ of close-packed methyl groups, with water clusters bridging neighbouring methanol hydroxyl groups through hydrogen bonding. This behaviour suggests that the anomalous thermodynamics of water–alcohol systems arises from incomplete mixing at the molecular level and from retention of remnants of the three-dimensional hydrogen-bonded network structure of bulk water.

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Figure 1: HH, XH and XX composite partial structure factors for a methanol–water mixture (70 mol% methanol).
Figure 2: Methanol–methanol site–site radial distribution functions.
Figure 3: Water–water OWOW radial distribution functions.
Figure 4: One of the simulated molecular boxes.

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Acknowledgements

S. D. is supported by the Edinburgh Chalmers Scholarship and the ORS award. Funding from the EPSRC Liquid Network and help from D. Bowron at an early stage of the experiments are gratefully acknowledged.

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Correspondence to A. K. Soper.

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Dixit, S., Crain, J., Poon, W. et al. Molecular segregation observed in a concentrated alcohol–water solution. Nature 416, 829–832 (2002). https://doi.org/10.1038/416829a

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