Nanostructure of pure iron anodically oxidized in borate buffer solution and annealed by infrared radiation

The behavior of oxide film on pure iron passivated in a borate buffer solution and subsequently radiated by infrared light (IR) was investigated in comparing to that by just IR annealing without passivation, and was evaluated by film structure, etc. The effect of thermal annealing over 250 degrees C was observed with gamma-Fe2O3 grain growth and sharp increase in surface roughness, film thickness and oxygen content. An ellipsometric parameter of tan psi was sensitively reflected by annealing effect, and tan psi curve had a shoulder at 150 degrees C for 5 min and a peak of tan psi was shifted from 350 nm to 450 nm in wavelength. This shift was also caused by the formation of gamma-Fe2O3, because the peak was also observed in tan psi of the bulk Fe2O3 family. Passivation effects at 800 mV prior to IR annealing on thickness and oxygen content changed at 150 degrees C, and decreased tan psi at 350 nm and excessive film growth over 250 degrees C, and increased oxygen content under 100 degrees C and surface roughness at 50-250 degrees C. The terrace width with atomic scale flatness was slightly increase by passivation prior to IR annealing at 50-250 degrees C, and the maximum terrace width reached larger than 10 nm by passivation and IR annealing at 100 degrees C for 30 min.     

Syntheses and characterizations of a new calixarene-porphyrin conjugate as electron transfer system

A new calixarene-based donor-acceptor system, cone conformer 1, was prepared for the first time. In this compound, the calix[4]arene serves to juxtapose a tri-chloroquinone acceptor near the porphyrin photo-donor plane. As to the conformational control, the cone conformer 1 gave two peaks of phenolic OH groups at 8.40 and 8.43 ppm. This shows that cone conformer 1 is stabilized by intramolecular hydrogen bonds. The fluorescence intensity of 1 was 35% of that for the control compound 2. This means the tri-chloroquinone group in 1 efficiently quenched the fluorescence of ZnP*. The shortest edge-to-edge separation of the chromophores of 1 is ca. 8 A (as judged by CPK models). This provides a new calixarene-based supramolecular system in which through-space donor-to-acceptor electron transfer is observed upon photoexcitation.     

Establishment and characterization of rat dental epithelial derived ameloblast-lineage clones

Teeth are the hardest tissues covered with enamel produced by ameloblasts. The ameloblast differentiation is controlled by sequential epithelial-mesenchymal interactions during tooth morphogenesis. However, the molecular mechanism of ameloblast differentiation remains unclear. To address this question, we developed an in vitro assay system to evaluate the molecular mechanism of amelogenesis. First, we established dental epithelium-derived clones from 6-day-old rat incisors and established that cells of the clone SRE-G5 were the largest producers of amelogenin mRNA. Next, we analyzed the effects of several chemicals on the amelogenin expression in SRE-G5 cells. Only mitogen-activated protein kinase (MAPK) activators enhanced amelogenin mRNA expression. This finding corresponded to the immunohistochemical data showing the presence of phosphorylated forms of p38, c-Jun N-terminal kinase (JNK), and extracellular signal-regulated kinase (ERK) during ameloblast differentiation. To examine the roles of MAPK signals, we compared the effects of anisomycin and sodium salicylate on the expression of tooth-related differentiation markers. Both anisomycin and sodium salicylate induced amelogenin, Abcg2, and Bmp4 mRNA and down-regulated p75NGFR mRNA. On the other hand, ALP, ectodin, Bmp2 and Fgf8 mRNA were up-regulated only by anisomycin. These results indicate that MAPK signaling functions, at least in part, as the inducer of ameloblast differentiation.     

Characterization of highly dispersed Ni/Al2O3 catalysts by EXAFS analysis of higher shells

The size and morphology of Ni/Al₂O₃ catalysts in the oxidic, reduced, and passivated state were determined by EXAFS analysis of the higher shells around the Ni atoms. In the oxidic state, the Ni cations were present in small NiO_x particles with predominant (111) plane. Below 4.5 wt% Ni loading, the NiO_x particles consisted of one Ni layer, and of two or three Ni layers above 4.5 wt% Ni. A Ni–Al contribution was observed in samples with low Ni loading. The layer which is in contact with the Al₂O₃ surface is affected by the support surface and its structure is highly distorted, while the other layers were not distorted and have a structure similar to that in bulk NiO. In the reduced state, the number of Ni metal atoms in the reduced Ni particles was smaller than 100 with a narrow distribution below a loading of 15.6 wt% Ni. Above this loading, the particle size suddenly increased and the distribution became wider. The distances and Debye–Waller factors were similar to those of bulk nickel which suggested a weak interaction between the particles and the support. In the passivated state, Ni kernels with 20–40 metal atoms were covered by a one layer thick NiO skin. This revised version was published online in June 2006 with corrections to the Cover Date.     

Solubility of propylene in semicrystalline polypropylene

Gas solubilities and polymer swelling in propylene and semicrystalline polypropylene system at temperatures of 323.2 and 348.2 K and pressures up to propylene's vapor pressure were measured. Pressure, specific volume, and temperature (PVT) measurements of polypropylene were carried out at temperatures from 313 to 573 K and pressures up 200 MPa. Two kinds of polypropylenes, which had different stereoregularities, were used for both solubility and PVT measurements. The solubilities were correlated with the Sanchez–Lacombe equation of state (EOS) with temperature‐dependent binary interaction parameters to within 5% average relative percentage deviation. Swelling ratios estimated with Sanchez–Lacombe EOS coupled with optimized interaction parameters were 20% lower than the experimental values. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 1134–1143, 2001     

Improvement in mechanical properties of poly(p‐phenylene sulfide) fibers by high‐tension multiannealing method

High‐tension multiannealing (HTMA) was applied to improve the tensile properties of poly(p‐phenylene sulfide) fibers, which was furthermore applied to the fibers produced and improved with the zone‐drawing and zone‐annealing treatments. The HTMA treatment was repeatedly applied to the fibers under the conditions of a 250°C temperature and an applied tension of between 201.0 and 188.0 MPa. As a result, at the 13th treatment the degree of crystallinity increased to 40%. On the other hand, the orientation factor of crystallites increased dramatically to 0.982 during the zone‐drawing treatment, but increased only slightly during the subsequent treatments of zone annealing and HTMA. The finally obtained fiber had a tensile modulus of 10.4 GPa and a tensile strength of 0.73 GPa. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 75: 1569–1576, 2000     

Thermal properties of solution flow-induced PVA crystals

Poly(vinyl alcohol) was crystallized from its aqueous solution under a steady-state flow with different conditions. Using a differential scanning calorimeter (DSC), the thermal properties of PVA precipitates obtained by the flow-induced crystallization were measured, showing a single melting peak in the DSC curve. The melting temperature of PVA crystallized depended on the rate of stirring, crystallization temperature, concentration of PVA, yield of precipitates, and morphology of the crystals. Particularly, there was a closer relationship between the melting temperature and the yield of precipitates, i.e., it was through the effect on the yield of precipitates that crystallization conditions influenced the melting temperature. Generally, with certain conditions, the higher the yield of precipitates, the lower the melting temperature. Moreover, using electron microscopy, it was observed that there were some structural differences between the inner and outer sides of a PVA crystal mat round stirrer and between film-shaped and block-shaped crystals, leading to different melting temperatures. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 64: 1337–1344, 1997     

Interactive aesthetic curve segments

To meet highly aesthetic requirements in industrial design and styling, we propose a new category of aesthetic curve segments. To achieve these aesthetic requirements, we use curves whose logarithmic curvature histograms (LCH) are represented by straight lines. We call such curves aesthetic curves. We identify the overall shapes of aesthetic curves depending on the slope of LCH α, by imposing specific constraints to the general formula of aesthetic curves. For interactive control, we propose a novel method for drawing an aesthetic curve segment by specifying two endpoints and their tangent vectors. We clarify several characteristics of aesthetic curve segments.