The interactions of furan and its hydrogenated derivatives (2,3-dihydrofuran, 2,5-dihydrofuran, tetrahydrofuran, and diethyl ether) with the isolated silanol groups at the surface of a highly dehydrated amorphous silica have been investigated by means of IR spectroscopy, at both constant and variable temperature. The adsorbate molecules studied form H-bonds of different strengths with surface silanols. With hydrogenated derivatives, the interaction involves the basic O atom, whereas with the aromatic furan molecule, the interaction probably occurs at the C═C double bond. The spectroscopic features of the stretching mode of H-bonded silanols change with the interacting molecule: classical correlations are observed. Because isolated silanols act as an ideal thermodynamic ensemble, the Langmuir model applies to all interactions. The fraction of silanols engaged in H-bonding can be measured from the decrement in intensity of the 3745 cm−1 band, so that corresponding optical isotherms can readily be drawn. The...
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