RESUMO
OBJECTIVES: The development of new bleaching agents with minimum concentration of hydrogen peroxide (HP), without adverse effects, and with bleaching effectiveness, has great clinical relevance. The aim of this study was to evaluate the bleaching efficacy and cytotoxicity of a new niobium-based bleaching gel, compared to already available HP-based gels. MATERIALS AND METHODS: For the bleaching efficacy analysis, 40 bovine incisors were randomly divided into 4 groups according to the established bleaching protocol: control, untreated; 35HP, 35% HP bleaching gel; 6HP, 6% HP bleaching gel; NbHP, niobium gel associated with 3% HP gel. The color variation was measured in a spectrophotometer and the values of ΔL, Δa, Δb, and ΔE obtained. For the cell viability assay by MTT, MC3T3 cells were exposed to bleaching gel extracts (1:500, 1:250, 1:125 dilutions; immediately and 24 h). Statistical tests were performed (P < 0.05). RESULTS: The color alteration for all bleaching gels was significant compared to control (P < 0.05), but the NbHP gel showed a significant ΔE than other gels, with expressive color alteration at 14 days (P < 0.05). The 35HP showed high cytotoxicity regarding control and the most groups in all periods and extracts analyzed (P < 0.05), while the NbHP showed greater cell viability than control in the immediate period, dilution of the 1:500 and superior to 6HP in the most extracts at 24 h. CONCLUSION: The new experimental niobium-based gel has bleaching efficacy similar to that of gels with a high concentration of HP, and it has high cytocompatibility. CLINICAL RELEVANCE: The use of this new generation of niobium-based whitening gel associated with a low concentration of hydrogen peroxide represents the possibility of a tooth whitening with lower dentin sensitivity.
Assuntos
Clareadores Dentários , Clareamento Dental , Animais , Bovinos , Géis , Peróxido de Hidrogênio/toxicidade , Nióbio/toxicidade , Clareadores Dentários/toxicidadeRESUMO
Mesoporous carbon (MC) derived from cassava starch was used to remove Acid Blue 113 azo dye from aqueous solutions. The influence of temperature, pH, ionic strength, and the adsorbent dose was investigated in a set of batch experiments. Experimental data showed that Acid Blue 113 adsorption was higher in the acid pH range than in the alkaline one, that dye adsorption increases when the ionic strength and temperature increase, and that adsorption results presented a good correlation with the Langmuir isotherm model. The adsorption capacity of MC was 295 mg g-1, at pH = 7.0 and 298 K, respectively. Zeta potential (ζ) showed the compression of the diffuse double layer of adsorbent with an increase in temperature and ionic strength, promoting the decrease of electrostatic repulsion between the negatively charged surface of the carbon particles and the anionic dye. Thermodynamic results demonstrate that the adsorption process was spontaneous and endothermic. Moreover, for the first time, this work has demonstrated that the pH, temperature, and ionic strength of the aqueous medium are also able to change the surface charge of carbon-based adsorbents and surely influence the adsorption capacity. Finally, the regeneration of the adsorbent by the photo-Fenton reaction regenerated the adsorption capacity of the adsorbent without generating secondary pollution to the environment.
Assuntos
Carbono , Poluentes Químicos da Água , Adsorção , Temperatura , Compostos Azo , Concentração Osmolar , Água , Concentração de Íons de Hidrogênio , Amido , CinéticaRESUMO
We demonstrate morphology and pore size dependence of silica nanoparticles (SNPs) synthesized via control of the iron oxidation state. In the absence of any Fe species, only spherical SNPs are produced, whereas in the presence of Fe³âº and Fe²âº ions, SNPs with rod-like and nanosheet morphologies, respectively, are formed. The average pore size increases from 1.7 nm in the absence of iron to 3.2 and 5.9 nm as Fe³âº and Fe²âº, respectively, were used during the synthesis. Both samples of SNPs synthesized in the presence of Fe²âº and Fe³âº have 0.2 wt% of tetrahedral iron in the silica framework, whereas most of the iron is in the silica extraframework, as verified by Mössbauer spectroscopy, UV-vis diffuse reflectance, FTIR, XRD data and TPR analysis. These Fe²âº and Fe³âº cations play a fundamental role in controlling these properties because they change the curvature and the surface charge density of CTAB micelles, thus favoring the spherical to rod-like transition. The rod-like shape was retained in Fe-containing samples, whereas a nanosheet-like morphology was produced in Fe²âº-containing samples due to the breakage of silica walls during the thermal treatment to remove the template. The control of the textural properties is interesting to allow the fabrication of selective photocatalysts for oxidation of different organic substrates.
Assuntos
Compostos Férricos/química , Compostos Ferrosos/química , Nanopartículas/química , Dióxido de Silício/química , Catálise , Íons/química , Nanopartículas/ultraestrutura , Oxirredução , PorosidadeRESUMO
A friendly environmental material for organic contaminants removal was prepared in this work: small particles of iron oxide dispersed over activated carbon from coffee waste for Fenton-like application. The materials were characterized by means of XRD, N2 physisorption, Mössbauer spectroscopy and H2 pulse titration. The composites showed very good catalytic performances for methylene blue organic dye oxidation. The small goethite particles are the predominant iron oxide phase in the composites. The apparent surface area is quite high and is not very affected after iron impregnation. ESI-MS studies revealed that the dye removal occurs through a Fenton-type system by the composite whereas for the activated carbon the dye removal occurs mainly via adsorption. The iron leaching from the catalysts was negligible, less than 0.5 ppm, which evidences the occurrence of a heterogenous oxidation process. The catalyst was very active for methylene blue oxidation and could be repeatedly used for at least 5 cycles. The catalyst was also active in the oxidation of other organic compounds, such as caffeine and atrazine.