Phase formation of Mn-doped zinc silicate in water at high-temperatures and high-pressures

Phase formation of Mn-doped zinc silicate (Zn₂SiO₄:Mn²⁺, ZSM) in high-temperature and high-pressure water was studied by in situ observations with a hydrothermal diamond anvil cell (HDAC). Precursor was prepared with zinc oxalate dihydrate, manganese oxalate, and silica, where the Zn/Mn/Si molar ratio was 192/8/120 to 199/1/120. Conditions of particle formation were at temperatures up to 650 °C and at pressures up to 1250 MPa. Precursors dissolved at temperatures of 145–203 °C and needle-like particles formed through homogeneous nucleation at temperatures from 357 to 374 °C, close to the critical point of water. The needle-like particles grew at growth rates of 0.5–3.8 μm/s and were identified to be ZSM as evident from their green luminescence. ZSM synthesized in supercritical water (400 °C for 180 min) by batch reactions had comparable luminescence with that of ZSM produced by solid-state reaction (1200 °C for 240 min) using the same precursor. The key finding in this work is that the precursors can be made to dissolve in near-critical water and that this allows ZSM to form via a homogeneous nucleation process.     

Solid‐state polymerization of melt‐spun poly(ethylene terephthalate) fibers and their tensile properties

The production of high modulus and high strength poly(ethylene terephthalate) fibers was examined by using commercially available melt‐spun fibers with normal molecular weight (intrinsic viscosity = 0.6 dL/g). First, molecular weight of as‐spun fibers was increased up to 2.20 dL/g by a solid‐state polymerization, keeping the original shape of as‐spun fibers. Second, the polymerized as‐spun fibers were drawn by a conventional tensile drawing. The achieved tensile modulus and strength of as‐drawn fibers (without heat setting) were 20.0 and 1.1 GPa, respectively. A heat setting was carried out for the as‐drawn fibers. Tensile properties of the treated fibers were greatly affected by the condition of the heat setting. This was related to the increase of sample crystallinity and molecular degradation during the treatments. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1791–1797, 2007     

Release Property of Progesterone from a Mixed-Base Suppository Consisting of Witepsol® W35 and Witepsol® E85

The mechanism of drug release from progesterone suppositories that consist of two types of hard fat (Witepsol® W35 and Witepsol® E85) was investigated. The strength, the thermodynamic characteristics, the surface structures, the drug release property, methylene blue penetration into suppositories, and change of surface structure after the dissolution test were employed for detecting characteristics of progesterone suppositories. The formulation with a mixing ratio of Witepsol W35 and Witepsol E85 at a 1:1 ratio showed the maximum strength value. The peak temperature of the suppositories showed a tendency to increase with increases in the ratio of Witepsol E85. The maximum height of the profiles measured with laser microscopy, from 20.8 μm to 29.2 μm, reached a maximum after 3 h of the dissolution test. When the suppositories were immersed in pH 7.4 phosphate buffer containing 0.5% methylene blue at 37°C, the penetrating area increased with time. The weight of the suppositories also increased with time. According to these findings, it was suggested that the release of drug from a mixed type of suppository containing progesterone was via the matrix and pores.     

Perception as evidence accumulation and Bayesian inference: Insights from masked priming.

The authors argue that perception is Bayesian inference based on accumulation of noisy evidence and that, in masked priming, the perceptual system is tricked into treating the prime and the target as a single object. Of the 2 algorithms considered for formalizing how the evidence sampled from a prime and target is combined, only 1 was shown to be consistent with the existing data from the visual word recognition literature. This algorithm was incorporated into the Bayesian Reader model (D. Norris, 2006), and its predictions were confirmed in 3 experiments. The experiments showed that the pattern of masked priming is not a fixed function of the relations between the prime and the target but can be changed radically by changing the task from lexical decision to a same-different judgment. Implications of the Bayesian framework of masked priming for unconscious cognition and visual masking are discussed. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Control of pit initiation sites on aluminum foil using colloidal crystals as mask

The electrochemical etching of aluminum foils using a physical mask of colloidal spheres was studied to directly control the initiation sites of pits independent of the surface activation state of the substrate. A two-dimensional array of colloidal spheres used as a mask was prepared by self-assembly on an aluminum substrate. The transfer of the hexagonally ordered pattern of self-assembled colloidal spheres to the aluminum substrate could be achieved by the selective electrochemical etching of an exposed aluminum surface. That is, etch pits were generated only in the triangular void space among the three spheres on the aluminum surface. Based on this process, the dispersibility of the initiation sites of pits was improved clearly in comparison with that for the conventional method. The density of pits could also be controlled by changing the diameter of spheres used as a mask.     

Sub-100-nm ordered silicon hole arrays by metal-assisted chemical etching

Sub-100-nm silicon nanohole arrays were fabricated by a combination of the site-selective electroless deposition of noble metals through anodic porous alumina and the subsequent metal-assisted chemical etching. Under optimum conditions, the formation of deep straight holes with an ordered periodicity (e.g., 100 nm interval, 40 nm diameter, and high aspect ratio of 50) was successfully achieved. By using the present method, the fabrication of silicon nanohole arrays with 60-nm periodicity was also achieved.     

Chemical constituents of the leaves of rabbiteye blueberry (Vaccinium ashei) and characterisation of polymeric proanthocyanidins containing phenylpropanoid units and A-type linkages

Chemical constituents of the leaves of rabbiteye blueberry (Vaccinium ashei READE) were investigated in detail. The major phenolic components were caffeoyl quinic acids, flavonol glycosides, flavan-3-ols and proanthocyanidins. Catechins and proanthocyanidins having additional phenylpropanoid units, such as cinchonains, kandelins and mururins, characterised the polyphenols of this plant. Among them, vaccinin A, an isomer of mururin A, was found to be a new compound, and the structure was characterised by spectroscopic methods. The most abundant polyphenols (11.3% of freeze-dried leaves) were oligomeric proanthocyanidins. Thiol degradation with mercaptoethanol indicated that the polymer was constituted of (+)-catechin and (−)-epicatechin as the terminal units and (−)-epicatechin, procyanidin A-2, and cinchonains Ia and Ib as the extension units. Mass spectral analysis suggested the presence of at least dodecamers with A-type linkages and phenylpropanoid moieties.     

Copper‐ion adsorption and gold‐ion reduction by polyphenols prepared by the enzymatic reaction of horseradish peroxidase

Polyphenols were synthesized via a horseradish peroxidase reaction from phenol, catechol, and pyrogallol for use as copper‐ion adsorbents. The molecular weights of the polyphenols ranged from about 1000 to 3000 g/mol. The hydroxyl group contents in the polyphenols from phenol, catechol, and pyrogallol were 5.9, 4.0, and 0.94 mol/kg, respectively, as determined by titration. The saturation binding capacity for copper ions of the polyphenols from phenol, catechol, and pyrogallol were calculated to be 1.44, 0.88, and 0.22 mol/kg, respectively, at pH 4.5. Copper ions were efficiently adsorbed via an ion‐exchange interaction by the synthesized polyphenols with vicinal hydroxyl groups, and those polyphenols could be applied to metal adsorption. Gold ions were selectively reduced by the phenol group in polypyrogallol in acid media to form gold particles. The reduced gold particles were eluted with a solution of 1.0M thiourea plus 0.5M HCl. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Synthesis of Silicon Carbide Ceramics Using Chemically Modified Polycarbosilanes as a Compaction Binder

A chemically modified polycarbosilane (PC) containing organofluoric groups (PCOCF) has been synthesized from PC and fluoroalkylmethyldimethoxysilane. PCOCF acts as an efficient compaction binder for SiC powders and as a coating material with excellent oxidation resistance in wet air. PCOCF-coated SiC powders also show excellent packing properties because of the organofluoric side chains, which give highly dense green compacts. PCOCF provides a high ceramic yield of 75% and highly dense SiC ceramics. Four-point bending strength increases and the scatter in strength values decreases significantly by PCOCF coating.     

High corrosion resistance of magnesium coated with hydroxyapatite directly synthesized in an aqueous solution

Anticorrosion coatings are crucial for practical applications of magnesium alloys, which are used to reduce the weight of vehicles, aircraft, electronics enclosures etc. Hydroxyapatite (HAp) potentially offers high corrosion resistance and no environmental toxicity because its thermodynamic structural stability is high and it is a basic component of bone. However, direct synthesis of HAp on magnesium in aqueous solutions has been a scientific challenge because Mg ions prevent HAp crystallization. A new method of direct synthesis of HAp on magnesium was developed using a Ca chelate compound, which can maintain a sufficiently high concentration of Ca ions on the magnesium surface to overcome prevention of HAp crystallization with Mg ions. Highly crystallized HAp coatings were successfully formed on pure magnesium and AZ series alloys. Corrosion behavior of HAp-coated pure magnesium was examined by cyclic dry and wet tests with 1 g m⁻² NaCl on the surface and polarization tests in a 3.5 wt% NaCl solution. A HAp-coated pure magnesium showed no noticeable corrosion pits after the dry and wet test. HAp-coated specimens showed 10³-10⁴ times lower anodic current density than as-polished specimen in the polarization test. The results demonstrate the remarkable anticorrosion performance of HAp coatings on magnesium for the first time.