Evaluation of ZnO/Carbon Xerogel Composite as a Photocatalyst for Solar and Visible Light Degradation of the Rhodamine B Dye

2021 ◽  
Vol 21 (4) ◽  
pp. 2292-2301
Author(s):  
Gabriela Spirandelli dos Santos ◽  
Clarice Moreira Goes ◽  
Juliana Giancoli Martins de Sousa ◽  
Nicolas Perciani de Moraes ◽  
Livia Chaguri ◽  
...  

This study is focused on the evaluation of the Rhodamine B photodegradation using ZnO/carbon xerogel composite as a photocatalyst, in order to enhance the photocatalytic process efficiency under visible light. The proposed synthesis employs tannin as a precursor for the carbon xerogel, which enhances the economic and environmental aspect of the composite. The synthesized materials have the hexagonal structure of the zinc oxide (wurtzite), which is homogeneously distributed on the carbonaceous matrix. The diffuse reflectance test shows that light absorption was significantly enhanced for the composite. The solar light-driven photodegradation results revealed that the synthesized composite achieved virtually complete degradation of the dye present in the solution in less than 3 h, in all concentrations tested. The results of visible light driven photocatalysis showed that the carbonaceous material presents better photoactivity than the pure oxide (70% and 40% degradation of Rhodamine B, respectively), due to the synergistic effect between the carbon xerogel and zinc oxide on the properties of the composite. The photocatalytic mechanism main active species are the photogenerated vacancies and superoxide radicals.

Author(s):  
Nicolas Perciani de Moraes ◽  
Ricardo Bertholo Valim ◽  
Robson da Silva Rocha ◽  
Maria Lucia Caetano Pinto da Silva ◽  
Tiago Moreira Bastos Campos ◽  
...  

2019 ◽  
Vol 886 ◽  
pp. 146-153
Author(s):  
Natkritta Boonprakob ◽  
Anchalee Masa-Ad

Indium sulfide and zinc oxide (In2S3-ZnO) films have successfully synthesized by doctor blading method coupling with low temperature precipitation-reflux rout. The weight ratio of In2S3 was varied from 0-70 wt.%. Physical characterization results obtained from various analytical techniques exhibit the well crystallinity phase of cubic β-In2S3 and wurtzite ZnO structure from XRD patterns. TEM micrograph of 35% In2S3-ZnO sample showed the small ZnO particles are embedded into β-In2S3. The obtained results exhibited the phase well crystallinity of cubic β-In2S3. A strong adsorption spectra shifted toward visible light region and the narrower optical band gap results of In2S3-ZnO composite films suggesting that synthesized samples could be used as the visible-light-driven photocatalyst. The photocatalytic activity of rhodamine B had been investigated over entire composite films under visible light illumination. It can be seen that the entire In2S3-ZnO composite catalyst films revealed degradation of rhodamine B performance obviously higher than pure ZnO and pure In2S3. Moreover, the highest photocatalytic activity was found from 35% wt. In2S3-ZnO film which showed 69.5% degradation within 4 h under visible light irradiation.


2014 ◽  
Vol 193 ◽  
pp. 154-159 ◽  
Author(s):  
Jianfeng Ma ◽  
Liangyin Li ◽  
Jing Zou ◽  
Yong Kong ◽  
Sridhar Komarneni

Nanomaterials ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 756 ◽  
Author(s):  
Jingjing Yang ◽  
Hongqing Zhu ◽  
Yuan Peng ◽  
Pengxi Li ◽  
Shuyan Chen ◽  
...  

TS-1/C3N4 composites were prepared by calcining the precursors with cooling crystallization method and were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), UV-Vis diffuse reflection spectrum (DRS) and nitrogen adsorption–desorption isotherm. The photocatalytic performance of TS-1/C3N4 composites was investigated to degrade Rhodamine B (RhB) under visible light irradiation. The results showed that all composites exhibited better photocatalytic performance than pristine TS-1 and C3N4; TS-1/C3N4-B composite (the measured mass ratio of TS-1 to C3N4 is 1:4) had best performance, with a rate constant of 0.04166 min−1, which is about two and ten times higher than those of C3N4 and TS-1, respectively. We attributed the enhanced photocatalytic performance of TC-B to the optimized heterostructure formed by TS-1 and C3N4 with proper proportion. From the results of photoluminescence spectra (PL) and the enhanced photocurrent, it is concluded that photogenerated electrons and holes were separated more effectively in TS-1/C3N4 composites. The contribution of the three main active species for photocatalytic degradation followed a decreasing order of ·O2−, ·OH and h+. The degradation products of RhB were identified by liquid chromatography tandem mass spectrometry (LC-MS/MS), and the possible photocatalytic degradation pathways were proposed.


2015 ◽  
Vol 448 ◽  
pp. 564-572 ◽  
Author(s):  
Fangfang Gao ◽  
Yan Zhao ◽  
Yawen Li ◽  
Gongjuan Wu ◽  
Yan Lu ◽  
...  

2011 ◽  
Vol 1352 ◽  
Author(s):  
Emilly A. Obuya ◽  
William Harrigan ◽  
Tim O’Brien ◽  
Dickson Andala ◽  
Eliud Mushibe ◽  
...  

ABSTRACTThe synthesis and application of environmentally benign, efficient and low cost heterogeneous catalysts is increasingly important for affordable and clean chemical technologies. Nanomaterials have been proposed to have new and exciting properties relative to their bulk counterparts due to the quantum level interactions that exist at nanoscale. These materials also offer enormous surface to volume ratios that would be invaluable in heterogeneous catalysis. Recent studies point at titanium dioxide nanomaterials as having strong potential to be applied in heterogeneous photocatalysis for environmental remediation and pollution control. This work reports the use of surface modified anatase TiO2 nanofibers with rhodium (Rh) nanoparticles in the photodegradation of rhodamine B (RH-B), an organic pollutant. The dimensions of TiO2 nanofibers were 150±50 nm in diameter and the size of the Rh nanoparticles was ~5 nm. The Rh-doped TiO2 catalyst exhibited an enhanced photocatalytic activity in photodegradation of rhodamine B under visible light irradiation, with 95 % degradation within 180 minutes reaction time. Undoped TiO2 did not show any notable phocatalytic activity under visible light.


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