Distrontium Cerate as a Radiopaque Component of Hydraulic Endodontic Cement

This study aimed to synthesize distrontium cerate (2SrO·CeO2: S2Ce) and evaluate its properties as an alternative component of the endodontic cement. S2Ce cement was prepared through calcination of strontium hydroxide and cerium carbonate. Subsequently, the crystal phase was confirmed using X-ray diffraction. S2Ce cement exhibited a rapid setting time (121 min) and achieved a high compressive strength (72.1 MPa) at 1 d after mixing, comparable to the compressive strength of a commercial mineral trioxide aggregate (MTA) cement (ProRoot MTA) after 28 d post mixing. However, the compressive strength decreased after 28 d of storage when the W/P ratio was 0.30–0.40 (p < 0.05). Ion dissolution test of the S2Ce cement showed that strontium ions were released after immersion in water (5.27 mg/mL after 1 d), whereas cerium dissolution was not detected. S2Ce exhibited approximately three times higher radiopacity (9.0 mm aluminum thickness equivalent) compared to the commercial MTA (p < 0.05). These findings suggest that S2Ce is a possible component for hydraulic endodontic cement that demonstrates a rapid setting and high radiopacity.

Effect of hydrogen, and vapors of water and organic compounds on the structure of Sr2CuO3

The effect of hydrogen, and vapors of water and the simplest organic compounds of various classes on the structure of strontium orthocuprate (Sr2CuO3) in the temperature range of 150–300 °C has been investigated. At temperatures up to 200 °C, hydrogen and water are embedded in the structure of Sr2CuO3 from the annealing atmosphere. Under these conditions, organic compounds are oxidized to form water followed by hydration of Sr2CuO3. It has been revealed that Sr2CuO3 is a catalyst for oxidation reactions. Water absorption > 2 wt.% provokes hydrolytic decomposition of Sr2CuO3 with the formation of strontium hydroxide and copper-richer cuprates (SrCuO2 and SrCu2O3). At a temperature of 300 °C, organic compounds partially reduce copper, which is also the cause of the decomposition of Sr2CuO3.

Antimicrobial Potential of Strontium Hydroxide on Bacteria Associated with Peri-Implantitis

Background: Peri-implantitis due to infection of dental implants is a common complication that may cause significant patient morbidity. In this study, we investigated the antimicrobial potential of Sr(OH)2 against different bacteria associated with peri-implantitis. Methods: The antimicrobial potential of five concentrations of Sr(OH)2 (100, 10, 1, 0.1, and 0.01 mM) was assessed with agar diffusion test, minimal inhibitory concentration (MIC), and biofilm viability assays against six bacteria commonly associated with biomaterial infections: Streptococcus mitis, Staphylococcus epidermidis, Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Escherichia coli, and Fusobacterium nucleatum. Results: Zones of inhibition were only observed for, 0.01, 0.1, and 1 mM of Sr(OH)2 tested against P. gingivalis, in the agar diffusion test. Growth inhibition in planktonic cultures was achieved at 10 mM for all species tested (p < 0.001). In biofilm viability assay, 10 and 100 mM Sr(OH)2 showed potent bactericidal affect against S. mitis, S. epidermidis, A. actinomycetemcomitans, E. coli, and P. gingivalis. Conclusions: The findings of this study indicate that Sr(OH)2 has antimicrobial properties against bacteria associated with peri-implantitis.

Effects of Nanostructure Additives on Supercooling and Freezing of Distilled Water

The phenomenon of supercooling, which prevents freezing of water below the freezing point, is an obstacle to the production of inexpensive ice. In the case of ice heat storage systems using bio-preservation, low-temperature refrigeration of food and ice capsules in the HVAC industry, the supercooled water in capsules that indirectly come into contact with the outside is one of the problems that must be solved to maintain energy costs and the quality of food or organs. To improve this, experimental evaluation of additives that serve as crude nuclear agents is needed. However, research on this area needs to be supported because the types of additives are limited and their physical properties are unstable. In this paper, the effect of distilled water containing an additive of average diameter nanometer size on solution (frozen) supercooled below the freezing point was investigated. The supercooling time and supercooling level of each specimen were analyzed after addition of kaolin, strontium hydroxide, oxidizing mineral and nano-sized single-wall carbon nanotubes (SWCNT) as mineral fine particles in the distilled water. As a result, it has been confirmed that kaolin and SWCNT can be used as nuclear materials to release supercooling of water. In addition, when kaolin, a mineral fine particle, is used as a nuclear material, its size affects the performance of nuclearization. This confirmed the impact of nuclear material particle size and structure on overcooled emissions.

Visible Light Responsive Strontium Carbonate Catalyst Derived from Solvothermal Synthesis

A single crystalline phase of strontium carbonate (SrCO3) was successfully obtained from solvothermal treatments of hydrated strontium hydroxide in ethanol (EtOH) at 100 °C for 2 h, using specific Sr:EtOH mole ratios of 1:18 or 1:23. Other solvothermal treatment times (0.5, 1.0 and 3 h), temperatures (80 and 150 °C) and different Sr:EtOH mole ratios (1:13 and 1:27) led to formation of mixed phases of Sr-containing products, SrCO3 and Sr(OH)2 xH2O. The obtained products (denoted as 1:18 SrCO3 and 1:23 SrCO3), containing a single phase of SrCO3, were further characterized in comparison with commercial SrCO3, and each SrCO3 material was employed as a photocatalyst for the degradation of methylene blue (MB) in water under visible light irradiation. Only the 1:23 SrCO3 sample is visible light responsive (Eg = 2.62 eV), possibly due to the presence of ethanol in the structure, as detected by thermogravimetric analysis. On the other hand, the band gap of 1:18 SrCO3 and commercial SrCO3 are 4.63 and 3.25 eV, respectively, and both samples are UV responsive. The highest decolourisation efficiency of MB solutions was achieved using the 1:23 SrCO3 catalyst, likely due to its narrow bandgap. The variation in colour removal results in the dark and under visible light irradiation, with radical scavenging tests, suggests that the high decolourisation efficiency was mainly due to a generated hydroxyl-radical-related reaction pathway. Possible degradation products from MB oxidation under visible light illumination in the presence of SrCO3 are aromatic sulfonic acids, dimethylamine and phenol, as implied by MS direct injection measurements. Key findings from this work could give more insight into alternative synthesis routes to tailor the bandgap of SrCO3 materials and possible further development of cocatalysts and composites for environmental applications.

Determination of Thermodynamic Parameters from the Dissolution of Strontium Hydroxide in Water and Mixed Solvent Systems by pH-Metric Method

In this study, saturated solutions of Sr(OH)2 in pure water and in mixed solvent systems (methanol - water, ethanol - water, 1-propanol - water, and 2-propanol - water) at two temperatures were prepared and titrated with standard HCl solution by using pH metry. Using these titration data, the molar solubility (s), solubilty product (Ksp) and Gibbs free energy (Go), entropy change (ΔSand#176;) and enthalpy change (ΔHand#176;) for dissolution of strontium hydroxide was determined. At room temperature (20and#176;C), the s, Ksp, ∆Go were found to be 4.28 x 10-2 mol L-1, 3.13 x 10-4 mol3L-3 and 19.70 kJ mol-1 respectively. The ΔHand#176; and ΔSand#176; of the reaction is 2.90 kJ mol-1 and – 60.80 J. mol-1 K-1. With increasing percentage content of organic solvent in mixed solvents, the molar solubility and Ksp decreased and ∆Go, ΔHand#176; and ΔSand#176; values increased. The results were correlated with the dielectric constant value of the solvents used in the study.