Sonochemical Preparation and Properties of Pt–3Y-TZP Nano-Composites

A uniformly aggregated 3 mol% yttria-stabilized tetragonal zirconia nano-powder (3Y-TZP) was prepared using thermal hydrolysis and the ultrasonic deagglomeration technique. The possibility of nano-engineering of Pt–3Y-TZP composite aggregates was studied. The as-synthesized Pt nano-particles (∼2 nm) were impregnated into zirconia nano-aggregates (20–45 nm). The morphology manipulation technique allowed production of the composite zirconia-based aggregates in which a significant fraction of the Pt particles was embedded into the densified zirconia aggregates. Using the colloidal technique and low-temperature (1150°C) sintering, we prepared the Pt-zirconia (0.5–1.5 wt% of platinum) nano-composites with average 3Y-TZP grain sizes of 120 nm, and with the platinum grains size in the range of 20–60 nm. The catalytic properties of composite Pt–3Y-TZP nano-composites were studied and described.     

Complex impedance and admittance of a silver-conducting glass

From the analysis of complex impedance and admittance data of (Agl)₇₅(Ag₄P₂O₇)₂₅ glass, an Ag⁺-ion conductor, it was revealed that the sample can be approximated by a seriesRC ₁ circuit at high temperature, with the capacitorC ₁ arising from the charge-carrier depleted region near the anode which develops as conduction proceeds, and by a parallelRC ₂ circuit at low temperature, with the capacitorC ₂ arising from the saturated value for ionic polarization of, say, the silver-iodine pairs as well as from the relaxation effect of the Ag⁺ ions for conduction. TheC ₁ andC ₂ values were found to be almost temperature-independent at peak frequencies of the distorted semicircles in respective complex planes, with the ratioC ₁/C ₂ as large as 10⁴.     

Incorporation of a well-defined polyether side-chain into segmented poly(ether-urethane urea) and examination for blood-compatibility

A new method of introducing a hydrophilic polyether side chain into segmented polyurethane using a polypropylene oxide macromer with 1,3-diol at one chain-end, which behaves as chain extender, is described. In this procedure, a molecular-designed side-chain is incorporated quantitatively and directly into polyurethane biomedical elastomer. The design is also of interest to biomaterials in artificial organs.     

The black layer underneath the anode of dc-biased silver metaphosphate glass

The black layer was generated underneath the anode when a gold-electroded silver metaphosphate glass, a silver-ion conductor, was dc biased with 500 V/cm or 250 V/cm at 140°C . It was concluded that this layer corresponded to the silver-depleted region formed by conduction of the silver ions towards the cathode. The blackening was ascribed to be due to the shortened Ag-O distance, caused by structural rearrangement within the region into the P₂O₅-like structure on biasing.     

Effects of light guides and optical filters for a high density lead glass counter

Effects of various light guides on energy resolution, position dependence of the output pulse and the hadron suppression factor were studied for a high density lead glass counter with particles of energies between 1 GeV and 16 GeV. The best hadron suppression factor was obtained for a configuration with a plastic light guide and a short wave cutoff filter at little expense to energy resolution. The energy resolution is worse at high energy and is dependent on the hit position of an incident particle for a BK7 light guide.     

Supramolecular Ligands for Histone Tails by Employing a Multivalent Display of Trisulfonated Calix[4]arenes

Post‐translational modification of histone tails plays critical roles in gene regulation. Thus, molecules recognizing histone tails and controlling their epigenetic modification are desirable as biochemical tools to elucidate regulatory mechanisms. There are, however, only a few synthetic ligands that bind to histone tails with substantial affinity. We report CA2 and CA3, which exhibited sub‐micromolar affinity to histone tails (especially tails with a trimethylated lysine). Multivalent display of trisulfonated calix[4]arene was important for strong binding. CA2 was applicable not only to synthetic tail peptides but also to endogenous histone proteins, and was successfully used to pull‐down endogenous histones from nuclear extract. These findings indicate the utility of these supramolecular ligands as biochemical tools for studying chromatin regulator protein and as a targeting motif in ligand‐directed catalysis to control epigenetic modifications.     

Real‐time histological imaging of kidneys stained with food dyes using multiphoton microscopy

We have developed a real‐time imaging technique for diagnosis of kidney diseases which is composed of two steps, staining renal cells safely with food dyes and optical sectioning of living renal tissue to obtain histological images by multiphoton microscopy (MPM). Here, we demonstrated that the MPM imaging with food dyes, including erythrosine and indigo carmine, could be used as fluorescent agents to visualize renal functions and structures such as glomerular bloodstreams, glomerular filtration, and morphology of glomeruli and renal tubules. We also showed that the kidneys of IgA nephropathy model‐mice stained with the food dyes presented histopathological characteristics different from those observed in normal kidneys. The use of the food dyes enhances the quality of tissue images obtained by MPM and offers the potential to contribute to a clinical real‐time diagnosis of kidney diseases. Microsc. Res. Tech. 78:847–858, 2015. © 2015 Wiley Periodicals, Inc.     

A facile approach to the fabrication of ultrathin polymer films and application to optical lenses

A facile approach to the fabrication of ultrathin polymer films on a flat or curved substrate is presented. Polymers with unsaturated pendant groups were spin-coated on a photoinitiator tethered surface, which was then photoirradiated and washed with a solvent. The obtained films were uniform, smooth (R_a < 0.2 nm) and exhibited robustness toward solvents. The thickness of the films was determined by the molecular weight of the coated polymer and was not dependent on the initial spin-coated thickness. A mechanism for the formation of the ultrathin film and application to optical lenses is presented.     

Titanium-aluminum oxynitride (TAON) as high-k gate dielectric for sub-32 nm CMOS technology

High-k insulators for the next generation (sub-32 nm CMOS (complementary metal-oxide-semiconductor) technology), such as titanium-aluminum oxynitride (TAON) and titanium-aluminum oxide (TAO), have been obtained by Ti/Al e-beam evaporation, with additional electron cyclotron resonance (ECR) plasma oxynitridation and oxidation on Si substrates, respectively. Physical thickness values between 5.7 and 6.3 nm were determined by ellipsometry. These films were used as gate insulators in MOS capacitors fabricated with Al electrodes, and they were used to obtain capacitance-voltage (C-V) measurements. A relative dielectric constant of 3.9 was adopted to extract the equivalent oxide thickness (EOT) of films from C-V curves under strong accumulation condition, resulting in values between 1.5 and 1.1 nm, and effective charge densities of about 10¹¹ cm⁻². Because of these results, nMOSFETs with Al gate electrode and TAON gate dielectric were fabricated and characterized by current-voltage (I-V) curves. From these nMOSFETs electrical characteristics, a sub-threshold slope of 80 mV/dec and an EOT of 0.87 nm were obtained. These results indicate that the obtained TAON film is a suitable gate insulator for the next generation (MOS) devices.     

Poly[(R)-3-hydroxybutyrate] formation in Escherichia coli from glucose through an enoyl-CoA hydratase-mediated pathway

In this study, a new metabolic pathway for the synthesis of poly[(R)-3-hydroxybutyrate] [P(3HB)] was constructed in a recombinant Escherichia coli strain that utilized forward and reverse reactions catalyzed by two substrate-specific enoyl-CoA hydratases, R-hydratase (PhaJ) and S-hydratase (FadB), to epimerize (S)-3HB-CoA to (R)-3HB-CoA via a crotonyl-CoA intermediate. The R-hydratase gene (phaJ(Ac)) from Aeromonas caviae was coexpressed with the PHA synthase gene (phaC(Re)) and 3-ketothiolase gene (phaA(Re)) from Ralstonia eutropha in fadR mutant E. coli strains (CAG18497 and LS5218), which had constitutive levels of the beta-oxidation multienzyme FadB(Ec). When grown on glucose as the sole carbon source, the cells accumulated P(3HB) up to an amount 6.5 wt% of the dry cell weight, whereas the control cells without phaJ(Ac) or fadR mutation accumulated significantly smaller amounts of P(3HB). These results suggest that PhaJ(Ac) and FadB(Ec) played an important role in supplying monomers for P(3HB) synthesis in the pathway. Furthermore, by using this pathway, a P(3HB)-concentration-dependent fluorescent staining screening technique was developed to rapidly identify cells that possess active R-hydratase.