Fine structure of tooth enamel in the yellowing human teeth: SEM and HRTEM studies

Objective : The aim of this study was to clarify an influence of the fine structure of human tooth enamel to the yellowing teeth. Materials and methods : Sound maxillary first premolars of 15–50‐year‐old females that were extracted for the orthodontic treatment were used as the test samples. The tooth enamel sections of these teeth that prepared by ion polishing were observed by scanning electron microscopy (SEM). Furthermore, the fine structure of substance filling the inter‐rod spaces was analyzed by high resolution transmission electron microscopy (HRTEM). Results : In white tooth, the inter‐rod spaces were observed at the width of about 0.1 μm, while in yellow tooth, the inter‐rod spaces were not clearly observed by SEM. HRTEM observations revealed for the first time that the inter‐rod spaces were filled with fine particles of poorly crystallized hydroxyapatite in the yellow tooth. In yellow tooth, it was considered that the color of the inner dentin was recognized due to the decrease of light scattering by filling the tooth enamel inter‐rod spaces. The generation of particles in the tooth enamel inter‐rod spaces was considered to be caused by the long‐time progression of calcification. Conclusions : These results suggested that the change in fine structure, filling in inter‐rod spaces of tooth enamel, was related to progression of calcification in the inter‐rod spaces with advancing age and one of the factors of yellowness of human tooth. Microsc. Res. Tech. 79:14–22, 2016. © 2015 Wiley Periodicals, Inc.     

Effects of Some Light Alloying Elements on the Oxidation Behavior of Fe and Ni-Cr Based Alloys During Air Plasma Spraying

The oxidation behavior of iron binary powders with addition of Si (1, 4 wt.%) and B (1, 3 wt.%) and that of a Ni-Cr based alloy powder with Si (4.3 wt.%), B (3.0 wt.%), and C (0.8 wt.%) additions during atmosphere plasma spray (APS) have been investigated. Analysis of the chemical composition and phases of oxides in the captured in-flight particles and deposited coatings was carried out. The results show that the addition of Si and B to iron effectively reduced the oxygen contents in the coatings, especially during the in-flight period at higher particles temperature. Ni-Cr based alloy powder with Si, B, and C additions reduced the oxidation of the base alloys significantly. Preferential oxidation and subsequent vaporization of Si, B, and C from the surface of the sprayed particles are believed to play a major role in controlling oxidation in the APS process.     

The effect of thickness on the steady-state creep properties of freestanding aluminum nano-films

To clarify the effects of film thickness on the creep properties of nano-films we conducted tensile creep experiments on freestanding aluminum films with thickness values in the range ～100–800 nm at room temperature. The nano-films showed typical creep behavior comprising transient, steady-state, and accelerated creep stages. The steady-state creep exponents of the 100–800 nm thick specimens were 0.84–2.7 in the stress range 30–120 MPa, which are close to the value for diffusion creep (1). Creep deformation clearly shows a thickness effect: the steady-state creep rate increases as the thickness decreases from 800 to 400 nm, shows a peak in the range 400–200 nm, and then decreases in the 200–100 nm thickness range. The creep experiments under a small stress of 1 MPa show a negative strain rate, indicating the presence of a driving force to reduce the surface area due to surface tension. The explanation for the thickness effect is as follows. Since the ratio of surface and grain boundary area to volume increases with decreasing thickness, diffusion creep along these paths is enhanced, resulting in an increase in the creep rate. As the thickness decreases to 200–100 nm, however, the surface tension effect to reduce the surface area becomes dominant, decreasing the creep rate. In addition, the creep rate of the nano-films is about two or three orders of magnitude smaller than that of the bulk material dominated by the dislocation creep mechanism.     

Thermodynamic Regularities in Perovskite and K2NiF4 Compounds

It has been found that the enthalpy of formation of perovskite compounds, Δ_fH° (ABO₃, B = transition metais), from binary oxides can be well characterized in terms the tolerance factor, t≡(r_A+ r_o)√2 (r_B+ r_o), where r_A and r_B are the radii of A-site ions with 12-coordination and B-site ions with 6-coordination, respectively, and Δ_fH°=−168 + 270(1 − t) kJ·mol⁻¹ for A^IB^VO₃, Δ_fH°=−125 + 1000(1 − t) kJ·mol⁻¹ for A^IIB^IVO₃, and Δ_fH°=− 90 + 720(1 − t) kJ·mol⁻¹ for A^IIIB^IIIO₃. Although the thermodynamic data of K₂NiF₄ compounds are not extensive, a similar regularity can be found when use is made of the radii of A-site ions with 9-coordination for the K₂NiF₄ compounds. These correlations will be quite useful in predicting.     

Processability and mechanical properties for binary blends of PP and LLDPE produced by metallocene catalyst

Processability at extrusion coating and mechanical properties of the films obtained are investigated by means of linear and nonlinear rheological measurements and tensile tests for blends of polypropylene (PP) and linear low‐density polyethylene (LLDPE). Both materials are produced by metallocene catalyst. The processability of PP is found to be improved by the addition of LLDPE; the blend shows low level of motor torque and head pressure in an extruder and small level of neck‐in as compared with pure PP. Further, the anisotropy of ultimate tensile strength, which is prominent for PP, is reduced by blending with LLDPE. As a result, the blend having 20 wt % of LLDPE shows appropriate properties in the molten state for extrusion coating and in the solid state as a film. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Oxide ionic conductivities of apatite-type lanthanum silicates and germanates and their possibilities as an electrolyte of lower temperature operating SOFC

Electrical properties of La_xM₆O_12+1.5x (M = Si, Ge) as an electrolyte for solid oxide fuel cell (SOFC) have been investigated. In La_xSi₆O_12+1.5x and La_xGe₆O_12+1.5x of x = 8–11, the highest conductivities were achieved at x = 9.7 (La_9.7Si₆O_26.55) and x = 9.0 (La_9.0(GeO₄)₆O_1.5), respectively. The conductivity of La_9.0(GeO₄)₆O_1.5 was higher than that of La_9.7Si₆O_26.55 in a temperature region higher than 700 °C, and the conductivity (2.4 × 10⁻³ S cm⁻¹) of La_9.7Si₆O_26.55 at 400 °C was higher than that (8.3 × 10⁻⁵ S cm⁻¹) of La_9.0(GeO₄)₆O_1.5. The power densities of SOFC (H₂ | Pt | electrolyte (thickness: 1 mm) | Pt | O₂) using La_9.0(GeO₄)₆O_1.5 as an electrolyte were 14.3 mW cm⁻² (700 °C) and 24.0 mW cm⁻² (800 °C). The corresponding SOFC using La_9.7Si₆O_26.55 was found to work even at lower temperatures of 400 and 500 °C with power densities of 0.011 and 0.12 mW cm⁻². The SOFC (H₂ | Ni–Sm_0.2Ce_0.8O_1.9 | electrolyte | Ba_0.5Sr_0.5Co_0.8Fe_0.2O_2.5 | air) using 0.3 mm thickness La_9.7Si₆O_26.55 electrolyte gave the 3.4 mW cm⁻² power density at 500 °C.     

Precision die-casting of optical MU/SC conversion sleeve

The performance of MU/SC conversion sleeve produced by bulk metallic glass (Zr₅₅Al₁₀Ni₅Cu₃₀) was examined. A precision die-casting method was applied to improve size accuracy. The size accuracy of the conversion sleeve produced by the precision die-casting method was ±1 μm, and optical insertion loss (Li) was less than 0.3 dB for a standard value. The wear resistance of metallic glass is improved by surface oxidation treatment in air at 673 K. The MU/SC conversion sleeve produced from bulk metallic glass has superior characteristics for optical parts.     

Inhibitory Effects of Cholesterol Derivatives on DNA Polymerase and Topoisomerase Activities, and Human Cancer Cell Growth

This paper describes the inhibitory activities of cholesterol derivatives such as cholesterol, sodium cholesteryl sulfate, cholesteryl-5α, 6α-epoxide, cholesteryl chloride, cholesteryl bromide, and cholesteryl hemisuccinate (compounds 1–6, respectively) against DNA polymerase (pol), DNA topoisomerase (topo), and human cancer cell growth. Among the compounds tested, compounds 2 and 6 revealed themselves to be potent inhibitors of animal pols, and the IC₅₀ values for pols were 0.84–11.6 and 2.9–148 μM, respectively. Compounds 2, 3 and 6 inhibited the activity of human topo II, with IC₅₀ values of 5.0, 12.5 and 120 μM, respectively. Compounds 2, 3 and 6 also suppressed human cancer cell (promyelocytic leukemia cell line, HL-60) growth, and LD₅₀ values were 8.8, 20.2 and 72.3 μM, respectively, suggesting that cell growth inhibition had the same tendency as the inhibition of topos rather than pols. Compounds 2 and 6 arrested the cells in S and G2/M phases, compound 3 arrested the cells in the G2/M phase, and these compounds also increased sub-G1 phase in the cell cycle. These results suggested that the effect of cell cycle arrest might be effective on both pols and topos activities. From these findings, the action mode of cholesterol derivatives as anti-cancer compounds is discussed.