Glancing-angle Raman spectroscopic probe for reaction kinetics at water surfaces

Abstract

We report glancing-angle Raman spectra acquired at the surface of aqueous dimethyl sulfoxide solutions and demonstrate that this technique can be used to measure the surface concentration of solutes. The presence of some solute molecules at the surface suppresses the intensity of the OH-stretching band of water there. We used this phenomenon to study the interfacial reaction of gas-phase ozone with aqueous NaX solutions (X = Br, I) by monitoring the decrease in intensity of the OH-stretching band of water over time. UV-VIS analysis of the product solutions indicates that X₃⁻, formed from X₂ evolved in the ozonation reaction, is the species most likely responsible for the decrease in OH-stretching intensity at the surface. The dependence of the rate of OH-Raman signal loss at the water surface on the bulk halide concentration is well described by a Langmuir–Hinshelwood kinetic model. The Langmuir–Hinshelwood parameters indicated that iodide has a ∼50 times greater propensity for the surface compared to bromide.