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Updated: Mar 1, 2026

Functionalization and Dispersion of Carbon Nanomaterials Using an Environmentally Friendly Ultrasonicated Ozonolysis Process
Published on: May 30, 2017
Probing the interphase "HO zone" originated by carbon nanotube during catalytic ozonation
Shuo Zhang1, Xie Quan2, Jian-Feng Zheng3
1Key Laboratory of Industrial Ecology and Environmental Engineering (MOE), School of Environmental Science and Technology, Dalian University of Technology, Linggong Road 2, Dalian 116024, China; Tianjin Key Laboratory of Aquatic Science and Technology, School of Environmental and Municipal Engineering, Tianjin Chengjian University, Jinjing Road 26, Tianjin 300384, China.
Abstract:
Carbon nanotube (CNT) is an attractive metal-free catalyst that can be explored in combination with ozone treatment. Using fluorescence microscopy image analysis, we investigated the production of hydroxyl radicals (HO) within the solid-liquid interphase for CNT-mediated catalytic ozonation. The visualized results suggest that HO was vastly generated via catalysis and accumulated within a surface region of the CNT (we defined this region as the interphase "HO zone"). In this region, using 7-hydroxycoumarin as a HO marker, the radical abundance was at least 1000 times higher than that in the aqueous bulk phase. Owing to the observed inhomogeneity of HO, the CNT/ozone system effectively decomposed perfluorooctane sulfonate that was fairly resistant to non-catalytic ozonation, and the decomposition kinetics was not much inhibited by tert-butanol as bulk-phase HO scavenger due to the remaining "HO zone" at surface region available for reaction. A longevity trial revealed the sustained formation of the interphase "HO zone" and strongly indicated that the graphitic structure may optimize the density of surface active sites responsible for the proliferation and local concentration of HO. CNT, with good catalytic efficiency, longevity and stability, is anticipated as the basis of future nanomaterials able to promote HO exposure in ozone treatment for advanced oxidation process.
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