Sustainable Mining: Reuse of Clay from Abandoned Areas in the South of Brazil for Ceramic Production Based on a Simplex Design.

The environmental impact of clay mining can be minimized using extractive mineral circularity practices. Combining the available knowledge of the characteristics of different clays with statistical tools was a decisive step for the improved use of mining resources. Through blends, all the mined materials can be incorporated to produce quality ceramic products. This study identified two types of clay from abandoned mining areas in the southern state of Santa Catarina, Brazil. These raw materials were valued together with plastic clay, which is widely used in the region, to develop 10 different formulations using a mixture design method. The clays were characterized using average granulometric distribution, mineralogical composition, and chemical, thermal and plasticity analyses. The specimens were shaped by extrusion, dried in an oven, fired in a muffle furnace and characterized based on their shrinkage, water absorption and compressive strength values. Two clays with varying characteristics-one with low workability and the other with a high silica content-exhibited difficulties (generating defects) in the extrusion shaping process, which compromised the final quality of the ceramic paste. Results showed that incorporating up to 45% by mass of the low-workability clay resulted in an increase in water absorption. The more siliceous clay improved dimensional control; however, its use at high contents (~80%) decreased the mechanical resistance. Nevertheless, when used in controlled amounts, these clays can be beneficial to the production of blocks and bricks because they have the potential to improve some properties of the finished ceramic products.

Tip and taper compatibility of accessory gutta-percha points with rotary and reciprocating instruments.

Objectives: This study was conducted to evaluate and compare the tip and taper compatibility of accessory gutta-percha points (AGPs) with various rotary and reciprocating instruments. Materials and Methods: Using a profile analyzer, tip and taper measurements were taken of 10 AGPs of each of the 14 models available from Odous de Deus and the 4 models available from Dentsply-Maillefer. Diameter measurements were taken at 1-mm intervals, from 3 mm from the tip (D3) to 16 mm. Results: Based on the mean values obtained, 3-dimensional (3D) models of the AGPs were drawn in Autodesk Fusion 360 and superimposed on 3D models of each instrument selected (Mtwo, Reciproc, RaCe, K3, and ProDesign Logic) to determine the compatibility between the instrument and the AGP. Data corresponding to the tips and tapers of the various AGPs, as well as the tip and taper differences between the AGPs and the instruments, were analyzed using descriptive statistics. The tapers of the AGPs were subject to the American National Standards Institute/American Dental Association No. 57 standard. The Odous de Deus extra-long medium and extra-long extra-medium AGPs were shown to be compatible with Mtwo, K3, and ProDesign Logic instruments with taper 0.06 and tip sizes 25 and 30, while the Dentsply fine and fine medium cones were compatible with Mtwo, RaCe, and K3 instruments with conicity of 0.04 and tip sizes 35 and 40. Conclusions: Both the Odous de Deus and Dentsply commercial brands included 2 AGP models with tip (D3) and taper compatibility with Mtwo, RaCe, K3, and/or Prodesign Logic instruments.

Impact of Particle Size on the Setting Behavior of Tricalcium Silicate: A Comparative Study Using ISO 6876 Indentation Testing and Isothermal Induction Calorimetry.

This study examines the impact of particle size on the setting behavior of tricalcium silicate powders. The setting behavior was evaluated using ISO 6876 indentation testing and isothermal induction calorimetry techniques. The objective was to compare the outcomes obtained from these methods and establish a correlation between particle size and setting characteristics. The cement pastes were manually mixed with a water-to-solid ratio of 0.66 for conducting indentation tests according to ISO 6876, while calorimetry measurements were performed using isothermal (conduction) calorimetry at room temperature. The findings demonstrate a significant influence of smaller particle sizes on accelerating the hydration process of cement pastes, resulting in a reduction of setting time by up to 24%. Moreover, the final setting times obtained through the indentation method closely approximate the inflection points of the acceleration curves acquired by calorimetry, with time deviations of less than 12% regardless of particle size.

Dissolution, bioactivity behavior, and cytotoxicity of 19.58Li2 O·11.10ZrO2 ·69.32SiO2 glass-ceramic.

Glass and bioactive glass-ceramic can be used in several applications. In bone growth where good bone/biomaterial adhesion was required, bioactive coatings for implants can improve bone formation. The glass and glass-ceramics of the LZS (Li2 O-ZrO2 -SiO2 ) system are very interesting because of their mechanical, electrical, and thermal properties. Very recently, their biological response in contact with human osteoblast has been evaluated. However, despite several initiatives, there are still no studies that systematically assess this system's bioactivity, dissolution, and cytotoxicity in vitro. This work aims to investigate the dissolution, bioactivity behavior, and cytotoxicity of LZS glass-ceramic. LZS glass-ceramics were produced from SiO2 , Li2 CO3, and ZrSiO4 by melting followed by quenching. The obtained glass frits were milled and uniaxially pressed and heat-treated at 800 and 900°C and submitted to physical-chemical, structural and mechanical characterization. Their dissolution behavior was studied in Tris-HCl, while bioactivity was performed in simulated solution body fluid (SBF). The cytotoxicity test was performed using glass-ceramic in direct contact with mesenchymal stem/stromal cells (SC) isolated from human exfoliated deciduous teeth. Structural and microstructural analyzes confirmed bioactivity. The results show that it was possible to produce bioactive glass-ceramic from LZS, proven by the formation of new calcium phosphate structures such as hydroxyapatite on the surface of the samples after exposure to SBF. The SC viability test performed indicated that the materials were not cytotoxic at 0.25, 0.5, and 1.0 mg/ml. The glass-ceramic system under study is very promising for a medicinal application that requires bioactivity and/or biocompatibility for bone regeneration.

Coal mining pyritic waste in Fenton-like processes: Raw and purified catalysts in Reactive Blue 21 dye discoloration.

Raw pyritic waste (RPW) from South Brazilian coal deposits and pure pyritic waste (PPW) were used as catalysts for organic dyes discoloration. Samples were characterized for their chemical, morphological, and structural properties. There was a significant content of Fe and S in both samples from the presence of iron sulfide. The average particle size is 10.9 µm for RPW and 7.4 µm for PPW, demonstrating that the beneficiation process could remove the larger quartz particles, interfered in the distribution, and average particle size. Smaller particle sizes promoted a larger surface area for the PPW. The influence of the pyritic waste in dosage, H2O2 concentration, and pH was evaluated, obtaining discoloration values above 95% for 0.5 g/L of pyritic waste, 2 g/L of H2O2, and pH 4.3 for both pyritic wastes. The degradation kinetics of the Reactive Blue 21 using the raw pyritic waste obtained a dye concentration removal above 93% in 90 min, with an iron release of 5.4 mg/L into the solution. Using PPW, the dye concentration removal was over 92% in 40 min, with the iron release of 15.5 mg/L into the solution. Discoloration rate for the PPW sample is 7 times greater than the rate obtained for RPW, indicating a faster decay rate for the purified sample. A decrease in discoloration efficiency is observed for PPW after 6 cycles of use, due to the higher concentration of iron leached into the medium. From the results, it was concluded that the raw pyritic waste has excellent potential for use as a catalyst for Fenton reaction, especially for dye-containing water discoloration, thus demonstrating the excellent applicability potential of pyritc waste in the degradation of organic pollutants in wastewater.

Effect of Feldspar Substitution by Basalt on Pyroplastic Behaviour of Porcelain Tile Composition.

This work aims to evaluate the effects of feldspar substitution by basalt on porcelain tile composition with respect to its porosity, flexural strength, and pyroplastic deformation. Three ceramic formulations with different amounts of feldspar substituted with basalt, 50% (C1), 75% (C2), and 100% (C3), were evaluated at three different temperatures, 1200, 1220, and 1240 °C. Specifically, the effect of replacing feldspar with basalt on the pyroplastic deformation of ceramic bodies was analysed using optical fleximetry. The porosity of C1 at 1200 °C was 19.3 ± 2.9%, while that of composition C3 was 22.2 ± 0.7% at 1240 °C. The flexural strength was strongly influenced by the temperature. For C1 at 1200 and 1240 °C, flexural strengths of 11.1 ± 0.6 and 22.2 ± 1.9 MPa, respectively, were obtained. Regarding fleximetry, thermal deformation decreased with an increase in the amount of feldspar substituted with basalt. It was observed that C2 and C3 deformed less at high temperatures than the other combinations of compositions and temperature, probably owing to the lower amount of residual glass phase present during cooling. Compositions with higher substitution amounts of basalt (i.e., C2 and C3) exhibited more stable thermal behaviour than C0.

Novel core-shell nanocomposites based on TiO2 -covered magnetic Co3 O4 for biomedical applications.

Magnetic Co3 O4 nanoparticles (NPs) have great potential for applications in biomedicine, as contrast enhancement agents for magnetic resonance imaging, or for drug delivery. Although these NPs are so attractive, their potential toxicity raises serious questions about decreasing cellular viability. In this context, Co3 O4 NPs were prepared via sol-gel method and encapsulated with a layer of TiO2 , a biocompatible oxide, and subjected to structural, magnetic and toxicity characterization. X-ray diffractograms of the samples demonstrate the successful synthesis of the spinel and Raman spectroscopy confirms the coating of the Co3 O4 spinel with TiO2 . The Co3 O4 cores showed a very intense superparamagnetic character; however, this behavior is strongly suppressed when the material is covered with TiO2 . According to the neutral red uptake assay, the coating of the cores with TiO2 significantly decreases the cytotoxic character of the Co3 O4 particles and, as it can be observed with the zeta (ξ) potential measurements, they form a stable colloidal dispersion at cytoplasmic pH. The effect of the thermal treatment enhances the biocompatibility even further, with no statistically significant effect on cell viability even at the highest analyzed concentration. The proposed pathway presents a successful sol-gel method for the preparation of Co3 O4 @TiO2 core-shell nanoparticles. This work opens up possibilities for future application of these materials not only for magnetic resonance imaging but also in catalysis and hyperthermia.