Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5204592 | Polymer Degradation and Stability | 2006 | 7 Pages |
Abstract
A series of polyaniline-anatase TiO2 (PANI-TiO2) nanocomposite powders with different PANI:TiO2 ratios were prepared by 'in-situ' deposition oxidative polymerization of aniline hydrochloride using ammonium persulfate (APS) as oxidant in the presence of ultrafine grade powder of anatase TiO2 cooled in an ice bath. And the solid-phase photocatalytic degradation of PANI-TiO2 nanocomposites was investigated under the ambient air in order to assess the feasibility of developing photodegradable polymers. The photodegradation of the composite powders was compared with that of pure PANI powders by performing weight loss monitoring, elemental analysis, FT-IR and UV-vis spectroscopy and X-ray photoelectron spectroscopy (XPS). The PANI-TiO2 nanocomposite powders showed highly enhanced photodegradation and the photodegradation increased with decreasing ratios of PANI:TiO2. A weight loss of about 6.8% was found for the PANI-TiO2 (1:3) nanocomposite; however, the weight loss of the PANI-HCl powder was only 0.3% after being irradiated for 60Â h under air. The photocatalytic degradation of the nanocomposite powders accompanied the peak intensity decrease in the FT-IR spectra at 1235Â cmâ1, attributed to C-N stretching mode for benzenoid unit, and the depigmentation of the powders due to the visible light scattering from growing cavities. The elemental analysis and XPS analysis of the composite showed that the bulk and surface concentrations of N decreased with irradiation. A possible mechanism for the photocatalytical oxidative degradation was also mentioned.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Liuxue Zhang, Peng Liu, Zhixing Su,