Photodegradation of methylene blue with a titanium dioxide/polyacrylamide photocatalyst under sunlight. Issue 19 (28th January 2016)

• Record Type: Journal Article
• Authors: Kazemi, Foad; Mohamadnia, Zahra; Kaboudin, Babak; Karimi, Zeinab
• Is Part Of: Journal of applied polymer science. Volume 133:Issue 19(2016)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2016-01-28
• Subjects: crosslinking -- hydrophilic polymers -- photopolymerization -- properties and characterization -- swelling; Polymers -- Periodicals; Polymerization -- Periodicals; 668.9
• DOI: 10.1002/app.43386
• Languages: English
• ISSNs: 0021-8995

Abstract

ABSTRACT: Hydrogels containing TiO2 nanoparticles (NPs) have photocatalytic properties and degrade pollutants under light. In this study, a polyacrylamide (PAAm) hydrogel was synthesized with TiO2 P25 NPs as the initiator, acrylamide as a monomer, and N, N ′‐methylene bisacrylamide as a crosslinker in aqueous media under sunlight. Fourier transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy, and transmission electron microscopy were applied to characterize the TiO2 /PAAm hydrogel. The effects of different synthetic conditions, such as the initiator concentration, crosslinker, and dilution, on swelling were investigated. The maximum swelling of the TiO2 /PAAm hydrogel was 45 g/g in the hydrogel synthesized with optimum conditions by 0.2% TiO2 . The photocatalytic degradability of the hydrogel was investigated with methylene blue (MB) as the pollutant target. Also, the effects of the pH and MB concentration were studied. Under optimum conditions, 95.00% of the MB was degraded by the TiO2 /PAAm photocatalyst after 5 h of irradiation under sunlight. The comparison of the results with those of the TiO2 P25 powder showed that the TiO2 NPs had better activity than the hydrogel, but unlike the hydrogel, the activity of these NPs decreased in each recycling time because of the aggregation of NPs. Finally, the hydrogel was recycled seven times without a considerable reduction in the degradation efficiency. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci.2016, 133, 43386. Abstract :