Photoreactivity of Carboxylated Single-Walled Carbon Nanotubes in Sunlight: Reactive Oxygen Species Production in Water

Very limited information exists on transformation processes of carbon nanotubes in the natural aquatic environment Because the conjugated pi-bond structure of these materials is efficient in absorbing sunlight photochemical transformations are a potential fate process with reactivity predicted to vary with their diameter, chirality, number and type of defects, functionalization, residual metal catalyst and amorphous carbon content, and with the composition of the water, including the type and composition of materials that act to disperse them into the aqueous environment. In this study, the photochemical reactions involving colloidal dispersions of carboxylated single-walled carbon nanotubes (SWNT-COOH) in sunlightwere examined. Production of reactive oxygen species (ROS) during irradiation occurs and is evidence for potential further phototransformation and may be significant in assessing their overall environmental impacts. In aerated samples exposed to sunlight or to lamps that emit light only within the solar spectrum, the probe compounds, furfuryl alcohol (FFA), tetrazolium salts (NBT2' and XTT), and p-chlorobenzoic acid (pCBA), were used to indicate production of 102, 02, and "OH, respectively. All three ROS were produced in the presence of SWNT-COOH and molecular oxygen (302). 102 production was confirmed by observing enhanced FFA decay in deuterium oxide, attenuated decay of FFA inthe presence of azide ion, and the lack of decay of FFA in deoxygenated solutions. Photogeneration of 02 and "OH was confirmed by applying superoxide dismutase (SOD) and tert-butanol assays, respectively. In air-equilibrated suspensions, the loss of 0.2 mM FFA in 10 mg/L SWNT-COOH was 85% after 74 h. Production of 102 was not dependent on pH from 7 to 11; however photoinduced aggregation was observed at pH 3.