Taxonomic Analysis involving Dental Microbiome during Orthodontic Treatment

Au/Pd/Al₂O₃ catalyst showed the best catalytic activity, and acetylene conversion and ethylene selectivity were 100% and about 80% at 40 °C, respectively.Tenofovir disoproxil (TD) has narrow absorption site mostly in upper intestinal tract where tenofovir rapidly decomposes. The aim of this work was to prepare and evaluate tenofovir disoproxil-loaded enteric microparticles (TDEMs) for the enhanced duodenal delivery. TDEMs were composed of TD, eudragit L-100 (EL) and ethyl cellulose (EC) as release-controlling polymers. For the physicochemical characterization, TDEMs were evaluated in terms of encapsulation efficiency (EE%), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR). The dissolution test was also performed while continuously changing the medium pH. The EE% of TD in TDEMs was good and more than 90%. The EC and EL formed a physically mixed structure and maintained their respective properties in TDEMs as confirmed by SEM image and FT-IR analysis. Combination of EL and EC gave higher enteric properties to TDEMs than the single use of EL or EC. The optimized TDEM (TD/EL/EC = 0.2/1/1, w/w/w ratio) yielded mean dissolution rate less than 10% in 1 h at pH 1.2, but completed dissolution with a dissolution more than 85% within 1 h at pH 6.5. Thus, the suggested TDEM would be promising enteric microparticles for the intensive delivery of TD to the duodenum.In this study, the highly ordered nanotube formation on beta typed Ti-xTa alloy surface was investigated. The Ti-xTa binary alloys were manufactured using a vacuum arc-melting furnace with varying Ta contents (10, 30, and 50 wt%), and then homogenized by heat treatment at 1050 °C for 1 h. The nanotube formation of Ti-xTa (x = 10-50 wt%) alloys were performed using a DC power source of 30 V in 1.0 M H₃PO₄ + 0.8 wt% NaF electrolyte solution for 2 hrs. The surface characterization was performed using field-emission scanning electron microscopy and energy-dispersive X-ray spectroscopy. The microstructure of Ti-xTa alloy showed martensite structure α', α″-phase, and a '-phase structure. As the Ta content increased, the needle-like structures of α' and α'-phase gradually disappeared and only the equiaxed structure of β-phase appeared. Nanotube morphology of Ti-xTa alloy changed according to Ta content. As the Ta content increased, the size of the nanotubes decreased and the number of the smaller nanotubes increased. In the cross-sectioned nanotube layer, the gap size between the nanotubes decreased as the Ta content increased.In this study, Molybdenum precursors were synthesized with Triphenylphosphine, 1,2-Bis(diphenylphosphino)ethane, Pyridine, 2,2-Bipyridine as a ligands. The molybdenum precursors was used for Hydrocraking reaction of Vacuum Residue (VR). Hydrocracking reactions were carried out under the 430 °C and H₂ pressure of 80 bar in an 100 ml high pressure reactor. New Molybdenum precursors were tested and their activities were compared with Mo-octoate. The Molybdeum-Phosphine precursor showed the best performances, high yield and low coke contents (below 0,5 wt%), in of hydrocracking for VR. To characterize the physicochemical properties of Moprecursor catalyst, various characterization techniques (NMR, XPS) were carried out. We confirmed that cokes in the reactor were contained the P atoms derived from ligand of Mo-precursor after hydrocracking of VR.SSZ-13 zeolite was modified by two kinds of post-treatment methods such as steaming and SiO₂ surface passivation (silylation) for ETP catalyst with high activity. The former steaming treatment was conducted in the range of 400-700 °C, whereas the latter surfaces passivation was applied to a chemical liquid deposition (CLD) technique that uses various silylation agents such as tetramethylorthosilicate (TMOS), tetraethylorthosilicate (TEOS), and tetrabuthylorthosilicate (TBOS). Catalysts were characterized by powder-XRD, ICP, Ar-phsisorption, solid-state 27Al MAS NMR, and NH₃-TPD, and their activities were tested in fixed bed reaction system. Regarding the effects of steaming temperature, the results show that a relatively higher selectivity is observed in SSZ-13 catalysts treated at proper steaming temperatures such as 450 and 500 °C compared to parent and other steam treated catalysts. For optimum surface passivation treatments for ETP reactions, one-step surface passivation using TEOS agents among various passivation agents led to enhanced propylene selectivity to 80% when compared with parent and other silylated SSZ-13 catalysts. However, a sequential passivation treatment with a TEOS agent was not highly affected by the reaction activity.The change of the Ir/Al₂O₃ catalyst before and after the reaction with ADN based low-toxicity monopropellant was confirmed. The catalyst were recovered after decomposition reaction with propellant in a monopropellant thruster at 350 °C preheating condition. Catalyst analysis was performed using a scanning electron microscope (SEM) and Brunauer-Emmett-Teller (BET) analyzer. The change of the catalyst specific devices.Mass production technique of nanoscale TiO₂ particle-embedded expanded polystyrene (EPS) balls with temperature-controlled melting method was developed, and the photocatalytic activity of TiO₂-embedded EPS (TiEPS) balls to suppress the excessive growth of Microcystis aeruginosa (M. aeruginosa) cultured from both indoor and outdoor experiments was verified under ultraviolet and solar light irradiation, respectively. According to the experimental results, the growth inhibition of M. aeruginosa was evidently observed by applying TiEPS balls, and increased proportionally with the surface area coverage of TiEPS balls. Based on the comparison of both specific growth rate (μ) and first-order degradation rate (k), the experimental cases using TiEPS balls with surface area coverage of 100% suppressed more significantly the growth of M. aeruginosa cultured from both indoor and outdoor experiments during the initial period of the experiment. However, through the whole experiment, both μ and k values between experimental cases using TiEPS balls and EPS balls with surface area coverage of 100% were not statistically different (p > 0.05). These results indicated that the photocatalytic degradation effect was dominant during the initial period of application, and the irradiation shading became dominant with the elapsed time. Therefore, the growth of M. aeruginosa can be suppressed due to both synergistic and combinational effects of photocatalytic degradation and irradiation shading under natural solar light. Based on the aforementioned results, self-floating TiEPS balls produced from this simple and cost-effective mass production technique can be readily applied to inhibit the excessive growth of harmful algae in the stagnant water body.The purpose of this study was to examine the effect of plasma treatment by treating the surface of Co-Cr alloy, Ti-6Al-4V alloy, and CP-Ti alloy as a material for denture metal frameworks with non-thermal atmospheric pressure plasma (NTAPP) and measuring their shear bond strength (SBS) with a heat-cured resin. 20 specimens were prepared for each of Co-Cr, Ti-6Al-4V, and CP-Ti alloys. Each metal alloy group was divided into the following subgroups depending on NTAPP treatment C (Co-Cr alloy without plasma), T (CP-Ti without plasma), A (Ti-6Al-4V alloy without plasma), CP (Co-Cr alloy with plasma), TP (CP-Ti with plasma) and AP (Ti-6Al-4V alloy with plasma). Specimens were treated with a metal conditioner and bonded to a denture base resin. SBS was measured using a universal testing machine. All data obtained were statistically analyzed using two-way analysis of variance (ANOVA), Tukey's honestly significant difference (HSD) test, and independent t-test. The mean values (SD) of SBS (MPa) were 10.31 (1.19) for C group; 12.43 (0.98) for T group; 13.75 (2.02) for A group; 13.53 (1.61) for CP group; 16.87 (1.55) for TP group; 17.46 (1.65) for AP group. The SBS of the AP group was the highest while that of the C group was the lowest. SBS of specimen treated with NTAPP was significantly increased regardless of metal alloy types (p less then 0.001). Within the limitations of this study, NTAPP can increases the SBS of Co-Cr alloy, CP-Ti alloy, and Ti-6Al-4V alloy with a denture base resin.Sulfonated poly(phenylene) oxide (sPPO) polymer is coated in a dopamine hydrochloride solution to prepare a highly durable, low-price polymer membrane for vanadium redox flow batteries (VRFBs). The polydopamine (PDA) coating on the sPPO membrane is confirmed using SEM and EDX analysis. sPPO coated with PDA exhibits decreased proton conductivity due to high resistance. However, VO+₂ reducibility tests shows that the chemical stability is improved due to the introduction of the PDA coating layer on the sPPO membrane, which has a chemical structure with poor durability in VO+₂ solution under the operating conditions of a VRFB. These results show that this polymer electrolyte membrane based on PDA-coated sPPO is a candidate for application in the long-term operation of VRFBs.Herein, we report the facile synthesis, characterization and visible-light-driven photocatalytic degradation of perforated curly Zn0.1Ni0.9O nanosheets synthesized by hydrothermal process. The X-ray diffraction (XRD) and scanning electron microscopy (SEM) studies confirmed the cubic phase crystalline structure and growth of high density perforated curly Zn0.1Ni0.9O nanosheets, respectively. As a photocatalyst, using methylene blue (MB) as model pollutant, the synthesized nanosheets demonstrated a high degradation efficiency of ~76% in 60 min under visible light irradiation. The observed results suggest that the synthesized Zn0.1Ni0.9O nanosheets are attractive photocatalysts for the degradation of toxic organic waste in the water under visible light.The purpose of this study was to investigate the surface observation of PEO-treated Ti-6Al-4V alloy after 2-step nano-mesh formation was investigated by FE-SEM, EDS, and XRD. Anodic oxidation treatment was performed on the electrolyte containing 0.8 wt.% Na/F and 1M H₃PO₄ to form a nanotube structure on the Ti-6Al-4V alloy. After removing the nanotube layer, PEO-treatment was performed on the electrolyte containing Mg and Zn ions. After forming the nanotubes, the nanomesh surface was obtained by removing the layer, and the surface roughness increased with cycle number of nanotube formation. Also, as the number of nanotubes increased, the anatase peak increased.The purpose of this study was to investigate the nanotube morphology changes of Ti-xNb-Ag-Pt alloys with Nb content. read more Ti-xNb-Ag-Pt was fabricated using arc melting vacuum furnace. The Ti- xNb-Ag-Pt ingot was further homogenized in an Ar atmosphere at 1100 °C for 1 h in a vacuum and then quenched at 0 °C. Nanotube formation on the samples was performed using anodization method with a DC power supply at 30 V for 2 h in 1 M H₃PO₄ +0.8 wt.% NaF at 25 °C. The surface morphology was observed using OM, FE-SEM, EDS, and XRD. In the microstructure of Ti-xNb-Ag-Pt alloy, needle-like structures on α and α″ gradually disappeared with increasing Nb, β-phase equilibrium structure appeared, and particle size decreased. The nanotube morphology of the Ti-xNb-Ag-Pt alloy changed according to the content of Nb. As the Nb content increases, the highly ordered nanotubes have changed to irregular nanotubes. The difference in dissolution area at the bottom of the nanotube was depending on the Nb content.