“…This difference can be explained by the synthesis procedure which led probably to a strong agglomeration 52–54 of the ZnO and Li 2 O structures. Furthermore, there is no correlation between BET surface area and the photocatalytic activity since our samples which suggests that the most important parameter is the presence of the doping agent and electron-hole mobility modification 55 . The decrease of specific surface area while the photocatalytic activity increases in the presence of Li atoms can be also attributed to a better adsorption of the organic dye on the surface of the photocatalysts and the decrease in the recombination rate, since more defects are created in the structure of the semiconductor material (ZnO) 56 at higher concentrations of doping agent.…”
Our study was focused on the synthesis of photocatalytic materials for the degradation of organic dyes based on the valorization of biomass resources. The biochar resulted from pyrolysis process of cherry pits wastes was activated by CO2 flow. Activated and inactivated carbon was used to obtain carbon-based photocatalysts impregnated with different zinc salt precursors. The activation of carbon had no significant influence on the photodegradation process. The doping procedure used Li2CO3 and Zn(CH3COO)2 of different concentrations to impregnate the biochar. The carbon-ZnO-Li2O based nanomaterials were analysed by TEM and SEM, while the presence of hexagonal wurtzite ZnO was investigated by XRD. The solid samples were analysed by PL at 360 nm excitation fixed wavelength to correlate their morphology with the optical and photocatalytic properties. The presence of Li atoms led to photocatalytic activities of the doped ZnO similar to the undoped ZnO obtained at higher concentrations of zinc acetate precursor.
“…This difference can be explained by the synthesis procedure which led probably to a strong agglomeration 52–54 of the ZnO and Li 2 O structures. Furthermore, there is no correlation between BET surface area and the photocatalytic activity since our samples which suggests that the most important parameter is the presence of the doping agent and electron-hole mobility modification 55 . The decrease of specific surface area while the photocatalytic activity increases in the presence of Li atoms can be also attributed to a better adsorption of the organic dye on the surface of the photocatalysts and the decrease in the recombination rate, since more defects are created in the structure of the semiconductor material (ZnO) 56 at higher concentrations of doping agent.…”
Our study was focused on the synthesis of photocatalytic materials for the degradation of organic dyes based on the valorization of biomass resources. The biochar resulted from pyrolysis process of cherry pits wastes was activated by CO2 flow. Activated and inactivated carbon was used to obtain carbon-based photocatalysts impregnated with different zinc salt precursors. The activation of carbon had no significant influence on the photodegradation process. The doping procedure used Li2CO3 and Zn(CH3COO)2 of different concentrations to impregnate the biochar. The carbon-ZnO-Li2O based nanomaterials were analysed by TEM and SEM, while the presence of hexagonal wurtzite ZnO was investigated by XRD. The solid samples were analysed by PL at 360 nm excitation fixed wavelength to correlate their morphology with the optical and photocatalytic properties. The presence of Li atoms led to photocatalytic activities of the doped ZnO similar to the undoped ZnO obtained at higher concentrations of zinc acetate precursor.
“…The influence of this HCl presence on photocatalysis is still unclear in the literature: There are only a low number of papers discussing its effect on photocatalysis, and some of them report it is detrimental [ 48 , 49 ], while others report it is beneficial [ 50 , 51 , 52 , 53 ]. HCl might be partly responsible for the low nanoparticle size [ 54 , 55 , 56 ], and there might be a correlation between HCl and surface properties that deeply influence photocatalysis [ 57 , 58 , 59 , 60 , 61 , 62 , 63 ]. A deep understanding of the role of the trapped HCl on the photocatalytic properties of this material is out of the scope of this work, but this phenomenon might deserve more attention in the future since, in our case, it does not seem to be detrimental for photocatalysis.…”
A new method for fast and simple synthesis of crystalline TiO2 nanoparticles with photocatalytic activity was developed by carrying out a classic sol–gel reaction directly under vacuum. The use of microwaves for fast heating of the reaction medium further reduces synthesis times. When the solvent is completely removed by vacuum, the product is obtained in the form of a powder that can be easily redispersed in water to yield a stable nanoparticle suspension, exhibiting a comparable photocatalytic activity with respect to a commercial product. The present methodology can, therefore, be considered a process intensification procedure for the production of nanotitania.
“…In our earlier works, a comparative study has been performed on different commercial catalysts of TiO 2 having different surface areas for the photodegradation of synthetic dyes [7,30], the results have shown that TiO 2 particles size and surface area are not the only factors influencing their photocatalytic activity, but it is rather surface properties such as surface acidity and the crystalline phase. Vorontsov et al [31] have also concluded, in their study on the photocatalytic activity of several synthesized samples of TiO 2 , that TiO 2 surface area and particle size are only secondary factors influencing photocatalytic activity, while other surface properties such as acidity, surface structure, and also extent of surface hydroxylation should play a major role in obtaining high performance of the photocatalytic process. In the case of ZnO, ZnO nanostructures of different morphologies were fabricated by Morales et al [32], and compared for dyes photocatalytic degradation.…”
Section: Kinetic Of Photocatalytic Degradationmentioning
Zinc oxide ZnO nanoparticles synthesized by sol-gel method and commercial titanium dioxide TiO2 were studied in the present work. The structural properties of the ZnO and TiO2 nanoparticles were determined by Fourier transform infrared (FTIR), X-ray diffraction (XRD) and Raman spectra techniques (RS). The average crystallite sizes were calculated by using the powder X-ray and were found to be 48 nm and 20 nm and the specific surface areas were about 1047 m 2 g −1 and 381 m 2 g −1 for ZnO and TiO2, respectively. The FTIR and Raman spectroscopy results have shown high purity of the ZnO and TiO2 samples and they are consistent with the one obtained from XRD. The ZnO and TiO2 nanoparticles were used as catalysts for the elimination of an azo dye, Mordant Violet 5 (MV5), in aqueous solution, by an advanced oxidation process which is heterogeneous photocatalysis. Synthesized ZnO was more efficient than commercial TiO2 to degrade MV5 under UV irradiation. The adsorption of MV5 on TiO2 and ZnO was found favorable by the Langmuir approach. The MV5 adsorption constant on TiO2 was higher than that obtained in the case of ZnO. The photocatalytic reaction of MV5 in presence of each catalyst was investigated at different concentration of the dye and at different conditions of pH. The solar radiation of MV5 in the presence of each catalyst was also tested.
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