Degradation of crystal violet over heterogeneous TiO2-based catalysts: The effect of process parameters

In this study, modified sol-gel method was employed to synthesize the pure and Zr-doped titania catalysts. Brunauer-Emmett-Teller (BET) method was applied to determine porosity, X-ray diffraction (XRD) analysis was used to study crystal structure, scanning electron microscopy (SEM) was used to investigate morphology and Fourier transform infrared spectroscopy (FTIR) was used to examine surface properties/total acidity of the obtained catalysts samples. Photocatalytic activity was tested in the reaction of crystal violet (CV) dye decolourization/degradation under UV light irradiation. The effects of several photocatalysis operational parameters were considered, such as catalyst dosage, initial dye concentrations, duration of UV irradiation treatment, as well as catalysts calcination temperatures and dopant amounts. The obtained results indicated faster dye decolourization/degradation with the increase of the catalyst dosage and the decrease of initial CV concentrations. The Zr-doping affects photocatalytic properties, i.e. CV decolourization/degradation of the prepared catalytic materials. Thus, addition of 5 wt.% of ZrO2 to titania increases photocatalytic effect for similar to 15% and addition of 10 wt.% of ZrO2 improves the photocatalytic efficiency of titania for nearly 30%

Effect of Fe2+ (Fe3+) Doping on Structural Properties of CeO2 Nanocrystals

We have measured the Raman scattering and magnetization of pure and Fe2+(Fe3+) doped CeO2 nanopowders at room temperature. The Raman scattering spectra revealed the existence of CeO2 fluorite cubic structure for all investigated samples. The Raman active mode at about 600 cm(-1), seen in all samples, can be ascribed to the CeO2 intrinsic oxygen vacancies. Additional Raman modes at 720 cm(-1), 1320 cm(-1) and 1600 cm(-1), which appear in the spectra of doped samples, can be assigned to maghemite (gamma-Fe2O3) cation deficient structure, to 2 omega(LO) IR-allowed overtone and two magnon structure, respectively. This implies that our powders are composed of mixed valence states and have defective structure. Presence of oxygen defect states and magnetic ions can be responsible for the observed ferromagnetism at room temperature in both pure and Fe doped samples.Symposium on Raman Scattering in Materials Science, Sep 15-19, 2008, Warsaw, Polan

Raman study of Ba-doped ceria nanopowders

A series of Ce1-xBaxO2-y (5 LT = x LT = 0.20) nanometric powders were synthesized by self-propagating room temperature synthesis. XRD and Raman scattering measurements were used to characterize the samples. at room temperature. All the samples are solid solutions with fluorite type structure with an average crystallite size about 5 nm. The redshift and asymmetric broadening of the Raman F g mode can be well explained with combined confinement and strain effects because of the nanocrystalline powders nature. The appearance of the additional peaks at similar to 560 cm(-1) and similar to 600 cm(-1), are attributed to extrinsic and intrinsic O2- vacancies in ceria lattice. Raman spectra of temperature treated Ce0.80Ba0.20O2-delta sample revealed the instability of this system

Hydrothermal Synthesis of CeO2 and Ce0.9Fe0.1O2 Nanocrystals

Pure and 10 mol% Fe3+ doped CeO2 nanocrystals were synthesized by hydrothermal method using two different basic solutions (NH4OH and NaOH). All the samples were calcinated at 140 degrees C and 200 degrees C. The characterization of crystalline structure, vibrational and optical properties was performed using X-ray diffraction, Raman spectroscopy and spectroscopic ellipsometry. The obtained results showed that the Fe-doped samples are solid solutions with different size of nanocrystals, very dependent on the synthesis temperature and type of basic solution. The Raman measurements demonstrated electron molecular vibrational coupling and increase of oxygen vacancy concentration whereas doping provokes a small decrease of optical absorption edge in comparison with pure ceria.International School and Conference on Photonics (PHOTONICA09), Aug 24-28, 2009, Belgrade, Serbi

Decolorization of crystal violet over TiO2 and TiO2 doped with zirconia photocatalysts

Titania based catalyst and TiO2 doped with zirconia were prepared by modified sol-gel method. The synthesized catalysts samples were characterized by BET, XRD, SEM and FTIR techniques. Photocatalytic activity was tested in the reaction of crystal violet (CV) dye decolorization/decomposition under UV light irradiation. The effect of several operational parameters, such as catalyst dosage, initial dye concentrations, duration of UV irradiation treatment and number of reaction cycles were also considered. The obtained results indicated faster dye decolorization with the increase of the catalyst amount and a decrease of initial CV concentrations. An influence of doping with zirconia on the physico-chemical properties of bare titania was studied. The doping procedure had affected photocatalytic properties of the final catalytic material, and had improved photocatalytic performances of doped catalyst on crystal violet decolorization/degradation in comparison to bare titania

Prospective of the LDI MS to characterization the corrosion products of silver-copper alloys on an example of the Ag-Cu-X (X- Zn, Pd, In) system

This work presents the perspective of applying the laser desorption/ionization mass spectrometry (LDI MS) for characterization the anode film of the Ag60Cu26Zn14, Ag58.5Cu31.5Pd10, and Ag63Cu27In10 alloys (at high concentrations of chloride ions in solutions). The reference LDI mass spectra of anode films of pure Ag and Cu have been used for the identification of product corrosion. Knowing the clusters detected in the reference spectra lead to the facilitating identification of the LDI mass spectrum of the sample and reduces the analysis time. The LDI MS analysis of these alloys revealed that the predominant corrosion product are AgCl (from AgnCln+1−/+, n = 1–3), and CuCl (from “superhalogen” CumCln− clusters, m = 1–2, n = 2–6); it also revealed Cu2(OH)3Cl (from Cu2(OH)(H2O)2+) and Cu2O (from Cu(H2O)+, Cu2O doped with chlorine). These results are in accordance with the X-ray diffraction and Raman analysis. The LDI MS spectra of alloys contain the additional peaks formed due to the mutual influences of different metals in the alloys (AgCuCl3− (AgCl-CuCl2−), AgCu2Cl4− (AgCl-CuCl-CuCl2−), and Ag2CuCl4− (AgCl-AgCl-CuCl−), which is consistent with the identified corrosion products. It should be noted that the LDI MS suggest the presence of CuCl2, which can be interpreted as the corrosion products retained in the porous films of alloys, and not detected by the other methods due to a small amount. The future theoretical and experimental studies of metal clusters, significant for metallurgy, can contribute that the LDI MS is becoming a powerful analytical tool for characterization the metal surfaces

Synthesis and characterization of new Ti–Bi2O3 anode and its use for reactive dye degradation

This paper reports the synthesis, characterization and application of a Ti–Bi2O3 anode for the electrochemical decolorization of the textile dye Reactive Red 2. The anode was synthesized by electrodeposition on a Ti substrate immersed in an acidic bismuth (III) solution at constant potential, followed by calcination in air at 600 °C. Thermogravimetric Analysis (TGA), Energy-dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD) analysis revealed that the electrodeposited material was predominantly metallic bismuth, which was oxidized to pure α-Bi2O3 during the calcination in air. SEM micrographs revealed that the Bi2O3 coat at the anode surface was inhomogeneous and porous. Reactive Red 2 was completely electrochemically decolorized at the synthesized anode in the presence of H2O2. The applied current density, H2O2 and Na2SO4 concentration, medium pH and initial dye concentration affected the dye decolorization rate. The optimal process parameters were found to be as follows: an applied current density of 40 mA cm−2 using a mixture of 10 mmol dm−3 H2O2 and 10 mmol dm−3 Na2SO4 at pH 7. The dye decolorization rate was shown to decrease as its initial concentration increased. The decolorization reactions were found to follow pseudo-first order kinetics

Synthesis and dielectric behavior of lead-free (Na0.5Bi0.5)(1-x)BaxTi1-yTayO3 piezoelectric ceramics

Solid solution of (Na0.5Bi0.5)(1-x)BaxTi1-yTayO3 in the composition range x = 0.06 and 0.0 LT = y LT = 0.05 were prepared by conventional ceramics sintering technique. These new group of lead-free piezoelectric ceramic were studied for their crystal structure, dielectric and piezoelectric properties. It is shown that the system possess pure perovskite phase in its as calcined state. A morphotropic phase boundary (MPB) between tetragonal and rhombohedral phases appears at x = 0.06 and y = 0.05. The room temperature measurements of dielectric and piezoelectric properties reveal that the obtained ceramics with MPB composition has potential for use as piezoelectric material

Synthesis and dielectric behavior of lead-free (Na0.5Bi0.5)(1-x)BaxTi1-yTayO3 piezoelectric ceramics

Solid solution of (Na0.5Bi0.5)(1-x)BaxTi1-yTayO3 in the composition range x = 0.06 and 0.0 LT = y LT = 0.05 were prepared by conventional ceramics sintering technique. These new group of lead-free piezoelectric ceramic were studied for their crystal structure, dielectric and piezoelectric properties. It is shown that the system possess pure perovskite phase in its as calcined state. A morphotropic phase boundary (MPB) between tetragonal and rhombohedral phases appears at x = 0.06 and y = 0.05. The room temperature measurements of dielectric and piezoelectric properties reveal that the obtained ceramics with MPB composition has potential for use as piezoelectric material

Crystal structure analysis of Nd-doped ceria solid solutions

This paper deals with Nd-doped ceria solid solutions: Ce(1-x)Nd(x)O(2-delta) with x ranging from 0 to 0.25. Six different powders were synthesized by applying the method based on self-propagating room temperature reaction (SPRT) between metallic nitrates and sodium hydroxide. The method is known to assure very precise stoichiometry of the final product in comparison with a tailored composition. Rietveld refinement was employed to get structural information on the. synthesized powder. An increase of Nd ion concentration increases the unit cell parameters and average bond distances. We have shown that all obtained powders were solid solutions with a fluorite-type crystal structure and all powder particles were of nanometric size (about 3 nm)