UV pretreatment has proven effective in enhancing the sulfur heterocycle specificity and saturation capacity of TiO2 adsorbents. Previous efforts in our laboratory have shown this effect to persist for over two weeks and were attributed to increased densities of surface hydroxyl groups as assessed by XPS and FTIR evaluations. This paper presents further evidence of the previous assertion by tracking the UV-induced conversion of adsorbed water and lattice oxygen into surface hydroxyls as monitored by XPS. Two different commercial TiO2 adsorbents (@ 163 and 70 m(2)/g) were investigated at various hydration levels as determined by TGA. Deconvolution of the XPS spectra demonstrated both the qualitative nature and quantitative conversion of adsorbed water and lattice oxygen according to the following stoichiometry, where one lattice oxygen is converted into two surface hydroxyls. O-(lattice)(2-) + H2O(ads) ->(uv)2OH(- ) Eight different reaction cases were examined using the 163 and 70 m(2)/g supports at four different hydration levels each. The measured stoichiometry for the above-noted conversion varied from 1.83 to 2.15 with an average value of 1.98 and a standard deviation of 0.10. Samples removed from the XPS chamber and stored in laboratory conditions showed that photo-generated surface hydroxyls could persist for over two weeks with or without handling.