Piezoelectric properties of vinylidene fluoride oligomer for use in medical tactile sensor applications

The piezoelectric effect of vinylidene fluoride (VDF) oligomer was evaluated with respect to its medical use as a new tactile sensor. VDF oligomer is a new substance that has a smaller number of VDF units and a lower molecular weight than poly(vinylidene fluoride) (PVDF); among the organic ferroelectrics, it has the largest reported remanent polarization. In this work, the performance of a prototype sensor device based on this material was evaluated. The piezoelectric coefficient of VDF oligomer was found to be greater than that of P(VDF/TrFE) copolymer; a film composed of VDF oligomer was thin and uniform. Based on the experimental results, possible applications of VDF oligomer in medical tactile sensors are discussed. This study confirms that VDF oligomer is a promising ferroelectric material for use in tactile sensors.     

Structure and magnetic properties of mono- and bi-layer graphene films on ultraprecision figured 4H-SiC(0001) surfaces

Monolayer and bilayer graphene films with a few hundred nm domain size were grown on ultraprecision figured 4H-SiC(0001) on-axis and 8 degrees -off surfaces by annealing in ultra-high vacuum. Using X-ray photoelectron spectroscopy (XPS), atomic force microscopy, reflection high-energy electron diffraction, low-energy electron diffraction (LEED), Raman spectroscopy, and scanning tunneling microscopy, we investigated the structure, number of graphene layers, and chemical bonding of the graphene surfaces. Moreover, the magnetic property of the monolayer graphene was studied using in-situ surface magneto-optic Kerr effect at 40 K. LEED spots intensity distribution and XPS spectra for monolayer and bilayer graphene films could become an obvious and accurate fingerprint for the determination of graphene film thickness on SiC surface.     

Crystal ice formation of solution and its removal phenomena on inclined cooled plate

Experimental studies for freezing phenomena of ethylene glycol solution on an inclined polyvinyl-chloride plate have been performed. It is found that the crystal ice formed on the inclined cooled plate is removed from the plate surface due to a buoyancy force acting on the crystal ice. It is shown that the crystal ice grows in a shape of sheet by joining with neighboring ice and that the ice slides along the inclined surface when it is removed. The onset of the ice removal condition is related to the cooling heat flux at the surface. The ice removal occurs more easily for the plate of large inclination than that of a small one.     

Adhesion control of fungal spores on solid surfaces using hydrophilic nanoparticles

Mold growth can trigger a variety of serious problems such as allergies and asthma. Designing surfaces that are unfavorable for the adhesion of fungal spores is considered an effective method to prevent fungal growth. In this study, the effect of hydrophilic surface treatment on the adhesion of fungal spores onto substrates was investigated using Aspergillus oryzae as a model fungus. The fungal spores that strongly adhered on the hydrophilic substrates under atmospheric conditions were easily removed by lightly washing by hand in water. These experimental results agreed well with thermodynamic predictions based on contact angle measurements. In addition, the removal ratio of the fungal spores on substrates coated with silica nanoparticles was higher than that on plasma-treated glass. It is believed that the contact area between a spore and substrate depended on the substrate roughness. Atomic force microscopy revealed that there was almost no adhesive force between the spores and glass substrate coated with silica nanoparticles. These results suggest that hydrophilic treatment using hydrophilic silica nanoparticles is more effective than hydrophilic plasma treatment to prevent fungal spore adhesion on glass substrates.     

Estimation of thermodynamic properties of solutes in silicon II

This paper proposes a computational method for estimating activity coefficients and interaction parameters of solutes in dilute solution taking into consideration the excess entropy of mixing using the grand canonical Monte Carlo simulation. The proposed method was applied to oxygen in silicon solution and its activity coefficient was estimated where a three-body potential was used as inter atomic potentials to reduce computational time. The solubility limit of oxygen was obtained by the reciprocal of the calculated activity coefficient. The calculated value was significantly changed by taking into consideration the excess entropy of mixing.     

Wave-optical evaluation of interference fringes and wavefront phase in a hard-x-ray beam totally reflected by mirror optics

The intensity flatness and wavefront shape in a coherent hard-x-ray beam totally reflected by flat mirrors that have surface bumps modeled by Gaussian functions were investigated by use of a wave-optical simulation code. Simulated results revealed the necessity for peak-to-valley height accuracy of better than 1 nm at a lateral resolution near 0.1 mm to remove high-contrast interference fringes and appreciable wavefront phase errors. Three mirrors that had different surface qualities were tested at the 1 km-long beam line at the SPring-8/Japan Synchrotron Radiation Research Institute. Interference fringes faded when the surface figure was corrected below the subnanometer level to a spatial resolution close to 0.1 mm, as indicated by the simulated results.     

Simultaneous Quantification of Plant Glyceroglycolipids Including Sulfoquinovosyldiacylglycerol by HPLC–ELSD with Binary Gradient Elution

Membrane lipids of photosynthetic organisms consist of glycerophospholipids and glyceroglycolipids. We investigated a method for the simultaneous quantitative analysis of neutral and acidic lipids using HPLC–ELSD, and quantified monogalactosyldiacylglycerol (MGDG), digalactosyldiacylglycerol (DGDG) and sulfoquinovosyldiacylglycerol (SQDG). Ten complex lipid classes were separated with a binary gradient system consisting of chloroform and methanol–acetone–water–acetic acid (30:60:9:1, v/v/v/v) with 0.3% triethylamine (pH 4), and were eluted within 16 min. The contents of SQDG in ten edible plants ranged from 3 to 101 mg/100 g, and were positively correlated to the neutral glyceroglycolipids contents.     

Influence of domain orientation on the mechanical properties of lead zirconate titanate piezoelectric ceramics

The influence of domain orientation on the mechanical properties of lead zirconate titanate (PZT) piezoelectric ceramics has been investigated using un-poled and poled PZT ceramics. High mechanical properties, e.g., high elastic modulus and compressive strength, were obtained for the polarized PZT ceramics due to strain hardening caused by more severe domain switching during the loading process, while low mechanical properties for the un-poled ceramics. Fracture mechanics of the ceramics were influenced by the direction of the tetragonal lattice structure since cracks propagate along the long axis of the tetragonal structure (c-axis). Using X-ray diffraction and electron back scatter diffraction analysis, the domain switching characteristics could be clarified.     

Thermal properties and dielectric relaxation of a multi‐component poly(ether‐co‐amide) based on polyamide‐12

DSC, dielectric relaxation and dynamic mechanical thermal analysis (DMTA) were carried out on two multi‐component poly(ether‐co‐amide) samples having different weight ratios of polyamide prepared by condensation polymerization with 12‐aminododecanoic acid, adipic acid and polyetherdiamine consisting of poly(tetramethylene oxide) and poly(propylene oxide). The melting temperature was lowered by an increase in the weight ratio of the polyamide segment. Three relaxation modes, α′, α_s and β, were found from dielectric relaxation measurements in different temperature ranges. The high temperature relaxation mode, α′, has a large dielectric constant, which disappears at the melting temperature of the polyamide crystal in the sample. The relaxation times for the segmental motion, α_s, were different for the samples, which is attributed to the difference in the composition of the uncrystallized polyamide segments in the amorphous domain. The glass transition temperature estimated from DMTA is located between those of constituting polymers. On the other hand, the activation energy of β‐mode observed at low temperatures is the same for samples with different polyamide ratios, which is attributed to the local motion of the polyether segments. The uncrystallized polyamide segments are miscible with the polyether segments, which results in a lowering of the glass transition temperature of the amorphous domain and enlarges the temperature range of the rubber state of the copolymer due to the high melting temperature of the polyamide segments. © 2016 Society of Chemical Industry