Abstract
Background: B-TiO2 was supported on the surface of iM16K glass bubbles to achieve a suitable density for the B-TiO2/iM16K composite hollow spheres. Aeration or stirring in the wastewater can lead to thorough mixing of photocatalyst and wastewater. Solid-water separation is relatively easy because the materials can float on the water surface while stopping aeration or stirring.
Methods: The iM16K glass bubbles were used to prepare boron-doped B-TiO2/iM16K composite hollow spheres through a sol-gel route. The materials were characterized by X-ray diffraction, scanning electron microscope, Fourier transforms infrared spectroscopy, UV-Visible diffuse reflectance spectrometry, and N2 adsorption-desorption techniques. The photocatalytic degradation of azophloxine on the composites was determined.
Results: The bandgap energy of the B-TiO2/iM16K composite was slightly less than 3.0 eV when the calcination temperature was below 500°C. The sample calcined at 350°C had a BET surface area of 88.6 m2/g, while the value of the sample calcined at 800°C was 1.2 m2/g. The maximum photocatalytic degradation efficiency was obtained for the sample calcined at 450°C, and nearly all of the original azophloxine molecules were decomposed after 120 min of irradiation. Photocatalytic degradation efficiency after 30 min of irradiation was enhanced from 18.8% to 47.9% when the B-TiO2 dosage increased from 100 to 800 mg/L.
Conclusion: Crystallization of anatase TiO2 was temperature-dependent, and the properties of BTiO2/ iM16K composite hollow spheres were affected by the phase composition of the boron-doped TiO2 layer. The change in calcination temperature can have a significant effect on the photocatalytic degradation of azophloxine. The production of hydroxyl radical depended on the photocatalytic activity of the B-TiO2/iM16K composite hollow spheres.
Keywords: Photocatalytic, hollow sphere, TiO2, calcination, azophloxine, composite.
Graphical Abstract
[http://dx.doi.org/10.1007/s10895-018-2319-z] [PMID: 30338428]
[http://dx.doi.org/10.1016/j.jclepro.2019.01.172]
[http://dx.doi.org/10.1021/cr00033a004]
[http://dx.doi.org/10.1016/S1389-5567(00)00002-2]
[http://dx.doi.org/10.1016/j.jphotochem.2018.07.007]
[http://dx.doi.org/10.1016/j.mssp.2018.11.025]
[http://dx.doi.org/10.1016/j.scitotenv.2019.06.172] [PMID: 31271990]
[http://dx.doi.org/10.1016/j.jclepro.2018.04.274]
[http://dx.doi.org/10.1016/j.apcatb.2016.08.012]
[http://dx.doi.org/10.1016/j.apsusc.2018.05.073]
[http://dx.doi.org/10.1016/j.jcat.2017.02.015]
[http://dx.doi.org/10.1016/j.apt.2018.02.034]
[http://dx.doi.org/10.1016/j.ultsonch.2019.02.026] [PMID: 31084793]
[http://dx.doi.org/10.1016/j.apcatb.2016.08.022]
[http://dx.doi.org/10.1016/j.jallcom.2018.11.398]
[http://dx.doi.org/10.1016/j.jallcom.2016.06.182]
[http://dx.doi.org/10.1007/s00339-018-1599-0]
[http://dx.doi.org/10.1515/jaots-2014-0109]
[http://dx.doi.org/10.2174/1573413714666180717112803]
[http://dx.doi.org/10.2174/1573413713666171117160154]
[http://dx.doi.org/10.1016/j.jclepro.2018.08.189]
[http://dx.doi.org/10.1016/j.cej.2019.122636]
[http://dx.doi.org/10.1016/j.jenvman.2019.109472] [PMID: 31521031]
[http://dx.doi.org/10.1016/S0030-4018(97)00469-0]
[http://dx.doi.org/10.1016/j.materresbull.2018.01.032]
[http://dx.doi.org/10.1016/j.ceramint.2013.07.143]
[http://dx.doi.org/10.1016/j.msec.2015.07.048]
[http://dx.doi.org/10.1016/j.mssp.2017.11.040]
[http://dx.doi.org/10.1063/1.323948]