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One dimensional (1D) ZnO nanorods were successfully synthesized via a facile solution route by refluxing their acetate precursors in diethylene glycol medium at 160°C. The as‐prepared ZnO nanorods were characterized by field emission scanning electron microscopy, X‐ray diffraction, and Fourier transform infrared spectroscopy. Experimental results demonstrated that the resultant products showed a 1D rod‐like hexagonal wurtzite crystal structure with diameters of about 5 nm and lengths of up to 100–200 nm. A possible growth mechanism of ZnO nanorods was tentatively proposed. Photocatalytic measurements demonstrated that the as‐prepared ZnO nanorods showed higher photocatalytic activities than the commercial photocatalyst TiO2 P25 nanoparticles. In addition, the effect of solution pH values and initial solution concentrations on the photocatalytic activities of as‐prepared ZnO nanorods was also evaluated. © 2014 American Institute of Chemical Engineers Environ Prog, 34: 74–80, 2015

Well-ordered TiO 2 nanotube arrays (TNAs) were fabricated by electrochemical anodization in a mixed organic electrolyte consisting of ethylene glycol and glycerol. The morphology, structure, crystalline phase, and photocatalytic properties of TNAs were characterized by using TEM, SEM, XRD and photodegradation of methylene blue. It was found that the morphology and structure of TNAs could be significantly influenced by the anodization time and applied voltage. The obtained tube length was found to be proportional to anodization time, and the calculated growth rate of nanotubes was 0.6 m/h. The microstructure analysis demonstrated that the diameter and thickness of the nanotubes increased with the increase of anodization voltage. The growth mechanism of TNAs was also proposed according to the observed relationship between current density and time during anodization. As expected, the obtained TNAs showed a higher photocatalytic activity than the commercial TiO 2 P25 nanoparticles.TiO 2 nanotube arrays (TNAs), anodization, organic electrolytes, photocatalysis

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