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Preparation Of Graphite / TiO 2 Catalyst And Its Photocatalytic Activity

Posted on:2017-01-09Degree:MasterType:Thesis
Country:ChinaCandidate:J L JiaFull Text:PDF
GTID:2131330485992848Subject:Environmental Science
Abstract/Summary:PDF Full Text Request
The combination of TiO2 with graphite(G) could solve the problem of recombination of the photogenerated electron-hole. In this work, G/TiO2 composite was synthesized via a sol-gel method, meanwhile, G/TiO2/foam-Ni and G/TiO2/PTFE were prepared by using the foam nikel as the support and PTFE latex as binder, and the photocatalytic performance of three photocatalysts has been investigated.The G/TiO2 composite were characterized by XRD, Raman, BET, XPS, SEM and TEM. The results showed that TiO2 in composite was anatase phase, and dispersed uniformly on the surface of the graphite with average diameter of 10 nm.The photoelectrochemical properties of G/TiO2 were investigated by UV-visible diffuse reflectance spectrum(DRS) and surface photovoltage spectrum(SPS). The results showed that the absorption edge of G/TiO2 exhibited a remarkable red-shift of20-25 nm and the stronger photoabsorbance over the whole visible light region as well as the significantly improved separation efficency of photogenerated electron-hole in comparison with the pristine TiO2.Photocatalytic systems were established with the methyl orange(MO) as the target pollutant, the 500 W Xenon lamp as simulated solar light and the G/TiO2,G/TiO2/foam-Ni and G/TiO2/PTFE as photocatalysts. The results showed that when the graphite content was 0.03 g, the calcination temperature was 350℃, the ratio of the powder G/TiO2 and PTFE latex of the G/TiO2/foam-Ni was 1:3, the ratio of the powder G/TiO2 and PTFE latex of the G/TiO2/PTFE was 1:5, the catalysts exhibited the best photocatalytic effect. Under illumination for 120 min, the MO degradation rate over G/TiO2, G/TiO2/foam-Ni and G/TiO2/PTFE was 77.5%, 85.1% and 95.6%, respectively.
Keywords/Search Tags:TiO2, graphite, immobilization, photocatalysis
PDF Full Text Request
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