Effect of BN nanoparticle content in SiC matrix on microstructure and mechanical properties of SiC/SiC composites

BN-nanoparticle-containing SiC-matrix-based composites comprising SiC fibers and lacking a fiber/matrix interface (SiC/BN + SiC composites) were fabricated by spark plasma sintering (SPS) at 1800°C for 10 min under 50 MPa in Ar. The content of added BN nanoparticles was varied from 0 to 50 vol.%. The mechanical properties of the SiC/BN + SiC composites were investigated thoroughly. The SiC/BN + SiC composites with a BN nanoparticle content of 50 vol.%, which had a bulk density of 2.73 g/cm³ and an open porosity of 5.8%, exhibited quasiductile fracture behavior, as indicated by a short nonlinear region and significantly shorter fiber pullouts owing to the relatively high modulus. The composites also exhibited high strength as well as bending, proportional limit stress, and ultimate tensile strength values of 496 ± 13, 251 ± 30, and 301 MPa ± 56 MPa, respectively, under ambient conditions. The SiC fibers with contents of BN nanoparticles above 30 vol.% were not severely damaged during SPS and adhered to the matrix to form a relatively weak fiber/matrix interface.     

Evaluation of MPN method combined with PCR procedure for detection and enumeration of Vibrio parahaemolyticus in seafood

Vibrio parahaemolyticus densities in spiked and naturally contaminated seafood samples were enumerated by the MPN method combined with a PCR procedure (MPN-PCR method) targeting the species-specific thermolabile hemolysin gene (tlh), and by the MPN method using subcultivation of alkaline-peptone-water (APW) enrichment culture on thiosulfate-citrate-bile-sucrose (TCBS) agar (MPN-TCBS method). In the samples spiked with both V. parahaemolyticus and V. alginolyticus, the numbers of V. parahaemolyticus enumerated by the MPN-PCR method were similar to, or higher than the numbers of spiked cells, whereas those enumerated by the MPN-TCBS method were below the numbers of spiked cells. In naturally contaminated seafood samples, the numbers of V. parahaemolyticus enumerated by the MPN-PCR method were higher than those by the MPN-TCBS method. In the case of the MPN-TCBS method, isolation of V. parahaemolyticus from some APW cultures was difficult because of the overgrowth of many colonies other than V. parahaemolyticus (e.g., V. alginolyticus) on TCBS agar. In contrast, the PCR technique could detect tlh from APW culture without isolation of V. parahaemolyticus, so the possibility of failing to obtain a positive result in APW culture by the MPN-PCR method was considered to be lower than that by the MPN-TCBS method. Furthermore, utilization of the PCR technique reduces the time and labor required for the biochemical identification tests used in the MPN-TCBS method. For the detection and enumeration of V. parahaemolyticus in seafood, especially for samples that show many colonies other than V. parahaemolyticus on TCBS agar, the MPN-PCR method may be more convenient and reliable than the MPN-TCBS method.     

Cover Image,Volume 97, Issue 8

The cover image, by Yuko Shimamura et al, is based on the Research Article Inhibitory effects of Japanese horseradish (Wasabia japonica) on the formation and genotoxicity of a potent carcinogen, acrylamide, DOI: 10.1002/jsfa.8055 .

     

Preparation of smooth and dense composite films consisting of MEHPPV and neat C60 by means of electrophoretic deposition

A procedure to prepare flat and dense composite films of a conjugated polymer poly[2-methoxy-5-(2′-ethylhexyloxy)-1,4-phenylene vinylene] (MEHPPV) and various amounts of neat C₆₀ by means of electrophoretic deposition from dilute suspensions is reported. It has been observed that deposition from suspensions containing both components results in pinhole-free films, which are applicable to photovoltaic devices, while inhomogeneous films are formed from the suspensions containing only one of the components. The applicability of electrophoretic deposition to obtain polymer-C₆₀ composite films showing photovoltaic effects has been successfully demonstrated.     

International mobility of researchers in robotics,computer vision and electron devices: A quantitative and comparative analysis

We investigated author information in scientific articles by approximately 7,000 researchers for a quantitative analysis of researchers’ international mobility. From top journals, we traced the movements of more than 2,200 researchers in the research domains of robotics, computer vision and electron devices. We categorized countries’ characteristics for the balance between the inflow and the outflow of researchers moving internationally. Flow patterns of international mobility confirm that the United States, China and India exhibit the greatest global flows of researchers, with Singapore and Hong Kong attracting remarkable numbers of researchers from other countries. International mobility focusing on institutions reveals that universities in Singapore receive as many foreign researchers as do research universities in the United States. Furthermore, firms and international collaborative research institutes act as alternative receivers to the universities in the electron devices research domain.     

Biocompatibility of a-C:H film coating for synthetic vascular graft

Amorphous hydrogenated carbon (a-C:H) films have many excellent properties such as biocompatibility, anti-corrosion, and chemical stability. Therefore, there are many reports on application of a-C:H film as surface modification technique for biomaterials. However, it is difficult to deposit a-C:H film on complex structures such as artificial heart blood pump and synthetic vascular grafts. In our previous work, we have developed an electrode which is adapted to such irregular structures for plasma CVD technique.In this study, a-C:H film was deposited on a synthetic vascular graft inner-wall by r.f. plasma CVD technique with cylindrical electrode. The purpose of such coating is improvement of biocompatibility of the vascular graft. The biocompatibility of the a-C:H film was evaluated by cytocompatibility and plasma protein adhesion. For the a-C:H film deposition, cytocompatibility and protein adsorbent of the vascular grafts were improved for biological response under cell culture with mouth fibroblasts and plasma proteins (albumin, fibrinogen, and globulin), respectively. This study indicates that the a-C:H films coatings is expected to surface modification for medical appliances.     

The cationic oligomerization of p-aminostyrene 2. Dimerization in the intial stage

Summary It was found that p-aminostyrene (PAS) could be oligomerized by using several aminium perchlorates as catalysts in acetonitrile to give a dimer D in the initial stage of the reaction and finally the isomerization oligomer 1 at the end, in quite similar manner to the preceding paper (1), where dimerization (hydroamination) is the main reaction in the initial stage. The pK_a values for the amines were evaluated by the indicator method, and the [H⁺]₀ and [MH⁺]₀ values were calculated from equilibrium equations. As a result, the rate increased with decreasing pK_a of the catalytic amine used and reached an overall constant value. From the relationships between the rate of the reaction and the [H⁺]₀ or [MH⁺]₀ values calculated numerically, however, it was determined that the rate was more affected by the [H⁺]₀ or [M⁺]₀ values rather than the pK_a of the catalyst. It was assumed that the reaction would be initiated by the electrophilic attack of MH⁺ on the double bond of the monomer. Three successive reactions were proposed for the dimerization step: slow protonation followed by subsequent fast reactions; amine addition to the resultant styryl cation and proton elimination. It was assumed that oligomerization might proceed via the same three successive reactions as proposed for the dimerization step. Received: 24 July 2000/Revised version: 8 September 2000/Accepted: 18 September 2000     

Decreasing the initial irreversible capacity loss of graphite negative electrode by alkali-addition

The effect of alkali function group contained in electrode binder was investigated. Carboxy methyl cellulose (CMC) improved the initial irreversible capacity loss in graphite negative electrode. Lithium acetate also improved the initial cycle efficiency. On the other hand, ethyl cellulose (EC) and hydroxyl propyl methyl cellulose (HPMC), which do not have a carboxylic group, did not decrease the reductive electrolyte decomposition. After charge and discharge cycle, the surface film composition on the electrode with CMC was less than on the electrode without CMC. This suggests that a carboxylic group in the binder acted as a catalyst and promoted the solid electrolyte interphase (SEI) formation which prevents the excess electrolyte decomposition on the graphite electrode.