We have used multiple-beam interferometry to study the temperature dependence of tert-butanol adsorption from vapor on mica, at an isolated surface and in a slit pore. The film thickness at one surface increases from 2 nm for 17 -24 ± C to .7 nm above the triple point T tr (25.5 ± C). Concomitantly, the surface separation at which the slit fills with liquid increases from 11 to 27 nm. These results show for the first time how a continuous triple-point wetting transition at one surface and suppression of the freezing transition in a slit pore affect capillary condensation near T tr PACS numbers: 68.15. + e, 64.70.Dv, 68.35.Rh, 68.45.Gd The thickness of films adsorbed from vapor depends on the relative strengths of substrate-adsorbent interactions and interactions between the molecules of the adsorbent [1]. Strong attraction between substrate and adsorbent often leads to complete wetting, where the absorbed film thickness t diverges as the vapor pressure approaches saturation. Wetting is common above the bulk triple point T tr of the adsorbent, where the film is fluid and similar in structure to the bulk liquid. At low temperatures, however, incompatibility in the structure of the adsorbed film imposed by the surface and that of the bulk crystalline phase often precludes complete wetting by the solid phase. The adsorbed film may grow to a thickness of a few molecular layers, and no further growth occurs unless nucleation of bulk solid takes place at or above saturation. Often there is thus a transition from incomplete wetting below T tr to complete wetting above T tr [2,3].There have been many experimental observations of wetting transitions near T tr [4][5][6][7][8]. In most cases, the transition to wetting is continuous with t diverging with a critical exponent of 21͞3 as T tr is approached along the solid-vapor coexistence line, i.e., t~DT 21͞3 [3][4][5][6][7][8]. This is expected theoretically on the basis of simple arguments involving long-range Van der Waals forces [2,3]. However, a first-order wetting transition at the bulk triple point has recently been reported for Ar and CH 4 on Au [9].One important example of a triple-point wetting transition is surface melting of bulk solids [10], where a fluid layer is formed on solid surfaces below the bulk melting point. In the presence of long-range, i.e., van der Waals forces, the thickness of the fluid layer should diverge with an exponent of 21͞3 as T approaches T tr .Other wetting transitions that have been discussed in the literature include wetting at the critical point T c [2,3]. A wetting transition at temperatures between T tr and T c requires strong temperature dependence of the substrateadsorbent interactions, and has been observed with shortchain alkanes adsorbed on water [11,12].In a slit, or a system of two parallel surfaces at a separation H, the phase behavior is more complex than at a single surface [13,14]. Complete wetting is no longer possible, since it would require t . H. Above T tr capillary condensation, a first-order vapor-liquid transiti...