The Effect of Calcination Temperature on Structure and Photocatalytic Properties of WO 3

Series of WO3/TiO2 nanocomposites were obtained by hydrothermal method followed by calcination in the temperature range from 400°C to 900°C. The characteristics of photocatalysts by X-ray diffractometry (XRD), scanning electron microscope (SEM), and diffuse reflectance spectroscopy (DRS) showed that increasing the calcination temperature from 400 to 900°C resulted in change of photocatalytic activity under UV-Vis light. Moreover, the amount of WO3 crystalline phase and amorphous phase in WO3/TiO2 aggregates, as revealed by XRD analysis, was dependent on the calcination temperature. The WO3/TiO2 samples with 8 mol% load of WO3 in respect to TiO2 calcinated at 500 and 800°C possess the highest photocatalytic activity in reaction of phenol degradation, which is about 1.2 and 1.5 times that with calcination at 400°C. The increase in calcination temperature above 400°C resulted in increase of WO3 crystallinity and reduction of the amount of amorphous phase in the nanocomposite structure. Moreover, the annealing of nanocomposites above 700°C decreases the value of optical band gap energies of obtained WO3/TiO2 nanomaterials

Surface and trapping energies as predictors for the photocatalytic degradation of aromatic organic pollutants

In this study, anatase samples enclosed by the majority of three different crystal facets {0 0 1}, {1 0 0}, and {1 0 1} were successfully synthesized. These materials were further studied toward photocatalytic degradation of phenol and toluene as model organic pollutants in water and gas phases. The obtained results were analyzed concerning their surface structure, reaction type, and surface development. Moreover, the regression model was created to find the correlation between the possible predictors and the photodegradation rate constants (k). From the studied factors, the trapping energy of charge carriers at the surface was found to be the most significant one, exponentially affecting the observed k. This resulted in the overall per-surface activity between the samples being in the order {1 0 1} > {1 0 0} > {0 0 1}. Further introduction of the surface energy (Esurf) to the regression model and the number of possible trapping centers per number of pollutant’s molecules (ntrap·n–1) improved the model accuracy, simultaneously showing the dependence on the reaction type. In the case of phenol photocatalytic degradation, the best accuracy was observed for the model including Esurf ·(ntrap·n–1)1/2 relation, while for the toluene degradation, it included Esurf2 and the S·n–1 ratio, where S is the simple surface area. Concerning different surface features which influence photocatalytic performance and are commonly discussed in the literature, the results presented in this study suggest that trapping is of particular importance.publishe

Antioxidative assessment of new trans-palladium (II) complexes in head and neck cancer

Background: Head and neck neoplasms stand for 6% of all malignant neoplasms worldwide. Chemotherapy has limited use due to the biological properties of the tumor (in the majority of cases moderately and poorly differentiated squamous cell carcinoma). The fundamental molecule used in treatment is cisplatin and its derivates, that can be associated with fluorouracil. The new chemotherapeutic agents are not in common use during the treatment of head and neck malignancies. However, the use of low molecular weight complexes Pd (II) carries the potential of being more effective in therapy. Material and Methods: Fifty-one patients, 30 men and 21 women (aged 52.9 ± 12.1 years) with head and neck cancer were included in the study. Fifty-one healthy subjects, 31 men and 20 women, (aged 54.1 ± 14.7 years) years formed the control group. Antioxidant enzymes, superoxide dismutase, and catalase activities in erythrocytes were examined. Results: An increased level of antioxidant enzymes was seen in the blood samples from patients with head and neck cancer after incubation with Pd (II) complex. In the group we obtained a statistically significant result p = <0.001. Discussion: That project may contribute to the development of new, more efficient head and neck cancer treatment strategies. In our opinion, the results can be used in the future to develop a valuable prognostic marker of the disease. This is important because the initial phase of cancer is asymptomatic. The search for factors involved in pathogenesis translates into economic benefits and makes therapy more effectiveness through the reduction of treatment expenses

Progress, Challenge, and Perspective of Bimetallic TiO2-Based Photocatalysts

Bimetallic TiO2-based photocatalysts have attracted considerable attention in recent years as a class of highly active catalysts and photocatalysts under both UV and Vis light irradiation. Bimetallic noble metal structures deposited on TiO2 possess the ability to absorb visible light, in a wide wavelength range (broad LSPR peak), and therefore reveal the highest level of activity as a result of utilization of a large amount of incident photons. On the other hand they can enhance the rate of trapping photoexcited electrons and inhibit the recombination process due to the capability of the storage of photoexcited electrons. Based on literature two groups of bimetallic photocatalysts were distinguished. The first group includes bimetallic TiO2 photocatalysts (BMOX), highly active under UV and Vis light irradiation in a variety of oxidation reactions, and the second group presents bimetallic photocatalysts (BMRED) exceptionally active in hydrogenation reactions. This review summarizes recent advances in the preparation and environmental application of bimetallic TiO2-based photocatalysts. Moreover, the effects of various parameters such as particle shape, size, amount of metals, and calcination on the photocatalytic activity of bimetallic TiO2-based photocatalysts are also discussed

Enhanced visible light photocatalytic activity of Pt/I-TiO2 in a slurry system and supported on glass packing

Highly photoactive I/TiO2, Pt/I-TiO2 nanocomposites were obtained using a hydrothermal and wet impregnation method. The incorporation of iodine and modification with 0.05 mol% of platinum leads to enhanced photocatalytic activity as compared to singly doped TiO2 due to the presence of impurity energy level in the structure of TiO2. X-ray diffraction, TEM microscopy, UV–Vis spectroscopy, X-ray photoelectron spectroscopy and BET methods showed that the most active photocatalyst had anatase structure, 187 m2/g specific surface area, absorbed UV–Vis light and contained 3 nm platinum particles. XPS analysis revealed that iodine exists in the form of I¯ and IO3¯ species and platinum was present as Pt and PtO2. The photocatalytic activity of Pt/I-TiO2 nanocomposite was maintained after 4 runs, suggesting stability and reusability of the obtained photocatalyst. The efficiency of degradation of model organic compound was measured in a slurry type photoreactor as well as in a fixed-bed photoreactor equipped with parabolic mirror with Pt/I-TiO2 immobilized on glass beads or glass Raschig rings.</p

Crystal Facet Engineering of TiO₂ from Theory to Application

Recently, the surface structure effect on photocatalytic activity has gathered increasing attention due to its reported influence on the charge carrier trapping and separation. Detailed control over the surface structure can be achieved by exposing the specific crystal facets. As a result, the photogenerated electrons and holes can be effectively separated between the different facets of semiconductor crystals. TiO2 is the most studied photocatalyst, with the particles exposing {0 0 1}, {1 0 0}, {1 0 1}, {1 1 0}, {1 1 1}, and {1 0 5} crystal facets. The performed studies have shown that the efficiency of the photocatalytic process strongly depends on the nature of the crystal facet exposed at the photocatalyst surface. In this regard, this chapter focuses on the comparison of possible surface-related parameters and photocatalytic activity of anatase, rutile, and brookite polymorphs with exposed different crystal facets. Particularly, computational data on their different possible surface structures are summarized, focusing on the geometry, energy, and possible reconstructions. This is followed by the general description of the hypothetical Wulff constructions and existing stabilization/synthesis strategies. Such an approach could help to further design, simulate, and optimize photocatalyst surface for efficient photoreduction and photooxidation processes