Breakup of non-newtonian emulsion jets

The breakup of non-Newtonian emulsion jets into drops was experimentally studied by ejecting both O/W and W/O emulsions vertically downward into stagnant air through nozzles. Breakup lengths of non-Newtonian emulsion jets were found to be almost equivalent to those of Newtonian jets. Experimental breakup data establish that the static surface tension of the oil phase can be used as the surface tension of W/O emulsion jets, whereas the dynamic surface tension of aqueous surfactant solutions is used as that of O/W emulsion jets. Diameters of drops formed from non-Newtonian emulsion jets are in good agreement with the prediction from the stability theory previously developed by the authors. When the rheological index in a power law model is appreciably smaller than unity and the Ohnesorge number is significantly large, however, drop sizes are larger than the prediction because of the profile relaxation in jets. The critical velocity of emulsion jets, either O/W or W/O emulsion, is significantly lower than that of homogeneous Newtonian jets.     

High-gain GaAs avalanche photodiodes with proton-implanted guard ring

A GaAs avalanche photodiode with a multiplication factor as high as 8000 was prepared by Zn diffusion and proton double implantation. The proton-implanted guard ring completely prevented edge breakdown, and multiplication occurred uniformly over the junction area. Dark current was proved to be due to a leakage current at the periphery between junction and implanted layer.     

Synthesis of rodlike polysiloxane containing polyol moieties derived from glucose with regularly controlled higher-ordered structure

A rodlike polysiloxane (3) containing polyol moieties derived from the sugar has been synthesized by reaction of an amine-functionalized rodlike polysiloxane (1) with gluconolactone (2) in the presence of triethylamine in DMF. Formation of 3 was estimated by the IR and ¹H NMR measurements. The functionality of 2 to the amino groups in 1 was ca. 75%, based on the ¹H NMR spectrum of the product. The XRD profile of 3 showed three peaks for a typical hexagonal phase, and the d-value of (100) peak of 3 was larger than that of 1, indicating the regularly controlled higher-ordered structure of 3.     

Ohmic contacts to Si-implanted InP

Ohmic contacts to Si-implanted, n⁺ layers on semi-insulating InP are investigated on the basis of the transmission line model. It is found that Au/Ni/AuGeNi/InP system shows a good ohmic behaviour with the specific contact resistance $\text{ρ}{}_{\mathrm{c}}\text{of}\text{2 × 10}{}^{\mathrm{?5}}\text{Ω}\text{cm}{}^2$ and the minimum contact resistance $\text{Z}{}_{\mathrm{c}}\text{of}\text{～ 2 × 10}{}^{\mathrm{?3}}\text{Ω}\text{cm}$ for a Si-dose higher than 2 × 10¹⁴ cm^?2 at 100 or 200 keV. The results indicate that, in the FET fabrication, at least 120 μm in length is necessary in order to obtain source and drain electrodes with the minimized resistance.     

Observation of GaAs—AlxGa1 — x as heterostructures and quantum-well-wire structures using backscattered electron image

As a microscale tool for observing GaAs-Al_x Ga_1–xAs heterostructures, backscattered electron (BE) images in the scanning electron microscope (SEM) were compared with conventional secondary electron (SE) images. BE images were found to be more sensitive to compositional differences between GaAs and Al_xGa_1–xAs and less sensitive to surface roughness. BE images have a spatial resolution of 10 nm or better. This method enables the nondestructive observation of ultrafine lateral periodic structures, such as quantum-well-wire (QWW) structures, fabricated by compositional disordering technology using focused Ga ion-beam (Ga-FIB) implantation into GaAs-Al_xGa_1–xAs material.     

Dynamic profile calculation of deposition resolution by high-energy electrons in electron-beam-induced deposition

The effect of the accelerating voltage of incident electrons on the resolution of electron-beam-induced deposition was investigated by a dynamic Monte Carlo profile simulator which includes the electron scattering in the already grown deposit structure. By simulating the deposition at two different accelerating voltages of 20 and 200 kV with an idealistic zero-diameter incident probe on a bulk substrate, it was revealed that the smaller size structures were attainable by 200 keV than by 20 keV. The effect of the substrate was also argued by comparing the above results with the simulation results obtained for a point-like starting substrate. Surprisingly, the shapes of the deposits grown on bulk substrates were reproduced well by the simulations starting from point-like substrates indicating the small effect of the substrate on the shape of deposits.     

Fabrication of Flexible and Transparent Conductive Nanosheets by the UV‐Irradiation of Gold Nanoparticle Monolayers

Conductive films that are highly transparent and flexible are extremely attractive for emerging optoelectronic applications. Currently, indium‐doped tin oxide films are the most widely used transparent conductive films and much research effort is devoted to developing alternative transparent conductive materials to overcome their drawbacks. In this work, a novel and facile approach for fabricating transparent conductive Au nanosheets from Au nanoparticles (AuNPs) is proposed. Irradiating an AuNP monolayer at the air–water interface with UV light results in a nanosheet with ≈3.5 nm thickness and ≈80% transparency in the UV–visible region. Further, the so‐fabricated nanosheets are highly flexible and can maintain their electrical conductivity even when they are bent to a radius of curvature of 0.6 mm. Fourier‐transform infrared and X‐ray photoelectron spectroscopy characterizations reveal that the transformation of the monolayer of AuNPs into the nanosheet is induced by the photodecomposition and/or photodetachment of the dodecanethiol ligands capping the AuNPs. Further, the UV‐irradiation of a hybrid monolayer consisting of AuNPs and silica particles affords the patterning of Au nanosheets with periodic hole arrays.     

Fabrication of lead-free piezoelectric (Bi<Subscript>0.5</Subscript>Na<Subscript>0.5</Subscript>)TiO<Subscript>3</Subscript>–BaTiO<Subscript>3</Subscript> ceramics using electrophoretic deposition

Electrophoretic deposition (EPD) process has certain advantages such as it can be applied for a mass production and also can be combined with magnetic crystal alignment technique. In this work, we prepared lead-free 85(Bi_0.5Na_0.5)TiO₃–15BaTiO₃ (85BNT–15BT) piezoelectric ceramics by conventional uniaxial pressing and EPD process. Various conditions were optimized such as suspension media, applied electrical field, and deposition time in order to yield dense green ceramics of 85BNT–15BT composition using EPD process. 85BNT–15BT ceramics prepared using EPD process revealed the Curie temperature of about 250 °C, coercive field of about 30 kV/cm, and piezoelectric constant (d ₃₃) of 75 pC/N. The EPD-processed samples exhibited structural and electrical properties similar to that of the conventionally processed one suggesting the successful fabrication of 85BNT–15BT piezoelectric ceramics by EPD method without composition deviation. This study lays a foundation on the fabrication of Bi-based lead-free piezoelectric ceramics by an alternative route other than the conventionally practiced solid-state reaction method maintaining the similar chemical composition, moreover, leaving a large space to explore more in the future.     

Bending fracture rule for 3D-printed curved continuous-fiber composite

Three-dimensional (3D) printing is an attractive technology to produce complex structures without the need for expensive tools and molds. Additives are usually incorporated with the plastic materials used in 3D printing to increase their strength and rigidity. In particular, carbon fiber-reinforced plastic (CFRP) shows promise as a material for use in 3D printing. However, the strength of CFRP after printing is still unclear, although it is known that its strength is affected by the plastic melting during printing. In this study, we analyzed the fracture behavior of CFRP specimens before and after bending to different curvature radii. From the experimental results, a fracture criterion that described the behavior of the materials by considering tensile and compressive loads was developed. The fracture mechanism was the same for CFRP specimens with different curvature radii. These results increase our understanding of the mechanical properties of CFRP materials used in 3D printing.     

Syntheses and properties of tetramethyl-p-silphenylenesiloxanealkenylmethyl-siloxane copolymers and their derivatives

$\text{Tetramethyl}\text{-p-}\text{silphenylenesiloxane}\text{alkenylmethylsiloxane}$ (TMPS/AMS) copolymers were snyhtesized from p-bis-dimethylhydroxysilylbenzene and a series of alkenylmethyldichlorosilanes as the starting materials. The alkenyl groups of the copolymers were vinyl, allyl, 2-(3-cyclohexenyl)ethyl, methacryloxypropyl and 3-bicycloheptenyl groups. The composition ranged from TMPS/AMS mole% ratio of $\text{92}\text{8}$ to $\text{83}\text{17}$ and the molecular weights were in the range 10⁴ to 10⁵. These copolymers were confirmed to have two compositions, one a certain length of TMPS segment and the other an AMS monomer unit, and that they could form films on the basis of the crystallization character of the TMPS segment. The melting temperatures of these copolymers decreased as the TMPS mole content decreased and as the alkenyl group contents were increased. The epoxidation reactions of these copolymers with m-chloroperbenzoic acid were carried out and the proportions of conversions of the alkenyl groups into epoxy groups varied depending upon the types of alkenyl groups involved. Cyclic olefin groups such as the 2-(3-cyclohexenyl)ethyl or the 3-bicycloheptenyl group were more easily epoxidized than the vinyl or allyl groups. The TMPS/dimethylsiloxane (DMS) graft copolymer could also be synthesized by the reaction of TMPS/vinylmethylsiloxane copolymer with dimethylhydrosilyl-terminated DMS oligomer in the presence of chloroplatinic acid acting as the catalyst.