Mechanical Behavior of Spray-Coated Metallic Laminates

Thermal spray (TS) coatings have been extensively utilized for various surface modifications such as enhancing wear/erosion resistance and thermal protection. In the present study, a new function of TS material is explored by studying its load-carrying capability. Due to the inherent microstructures containing voids and interfaces, it has been presumed TS materials were not suitable to bear loads. However, the recent advances in TS technology to manufacture near fully dense TS coatings have expanded their potential applications. In the current experiments, TS nickel coatings are deposited onto metallic substrates, and their mechanical behaviors are closely examined. Based on the measured data, the estimated elastic modulus of TS Ni is about 130 GPa (35% less than bulk value), and the maximum tensile strength is about 500 MPa (comparable to bulk value). It was found that such a high value is attainable because the coating is deposited onto a substrate, enabling a load-transfer mechanism and preventing coating failure at a much lower stress level. Three distinct deformation stages are identified to describe this behavior. Such a clarification is critical for enabling TS process to restore structural parts as well as to additively manufacture load-bearing components.     

Support Effects of Carbon on Pt Catalysts

Experimental evidence for support effect of carbon are summarized for Pt or PtRu catalysts supported by carbon nanotubes and graphene as well as for model catalysts of Pt/HOPG (highly oriented pyrolytic graphite). The electronic modification of Pt catalysts by the support effect is explained by a π–d interaction at the interface between graphitic surface and Pt. The interface interaction is related to non-bonding localized states of carbon, which are observed by scanning tunneling spectroscopy near defects or the doped-nitrogen atom on HOPG. The localized states propagate to a few nanometer regions behaving as acid and basic sites.     

Paper-structured catalyst with porous fiber-network microstructure for autothermal hydrogen production

Copper–zinc oxide catalyst powders were supported on a microstructured matrix composed of ceramic fiber-network by a papermaking technique. As-prepared catalyst materials, called paper-structured catalyst, were applied to the autothermal reforming (ATR) of methanol to produce hydrogen for fuel cell applications. The paper-structured catalyst demonstrated higher methanol conversion and lower undesirable carbon monoxide concentration, as compared with commercial catalysts. Besides, excellent catalyst durability was exhibited by the suppression of Cu sintering during the ATR reaction. The paper-structured catalyst showed remarkable superiority in methanol conversion even in the case of using sintered catalysts. Such features were possibly induced by the unique fiber-network microstructure (average pore size: ca. 20 μm and porosity: ca. 50%) of the paper composites, which may allow the effective transfer of heat and reactants to the catalyst surfaces. The porous paper-structured catalyst is expected as a promising catalytic material for improving the practical performances in the catalytic gas-reforming process.     

Characterization and gas‐permeation properties of crosslinked diacetylene‐containing polymer membranes from ferulic acid

Thermally and UV crosslinked poly[propargyl(3‐methoxy‐4‐propargyloxy) cinnamate] (PPOF) were investigated in terms of their physical, thermal, optical, and gas‐permeation properties. The crosslinked membranes had high gel contents because of the formation of a diacetylene network. The wide‐angle X‐ray diffraction patterns showed that all of the membranes were amorphous in structure, regardless of the type of crosslinking reaction. The membrane density increased after the crosslinking reaction; this suggested that the free volume of the crosslinked membrane was lower than that of the untreated membranes. Drastic color changes in the membranes were also observed because of the highly conjugated crosslinked network of diacetylene. In addition, the conjugation caused by diacetylene crosslinking led to visible absorption within the range 400–600 nm. The gas permeation of the crosslinked membrane was reduced compared with that of the untreated membranes. In particular, the gas permeability of the thermally crosslinked membrane was lower than that of UV‐irradiated membrane. On the basis of this result, the degree of crosslinking by thermal treatment was higher than that of UV irradiation. Hence, the crosslinked PPOF membranes showed improved gas‐barrier properties due to the high conjugation of the crosslinked diacetylene network induced by thermal treatment and UV irradiation. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Lessons from Mouse Models of High-Fat Diet-Induced NAFLD

Nonalcoholic fatty liver disease (NAFLD) encompasses a clinicopathologic spectrum of diseases ranging from isolated hepatic steatosis to nonalcoholic steatohepatitis (NASH), the more aggressive form of fatty liver disease that may progress to cirrhosis and cirrhosis-related complications, including hepatocellular carcinoma. The prevalence of NAFLD, including NASH, is also increasing in parallel with the growing epidemics of obesity and diabetes. However, the causal relationships between obesity and/or diabetes and NASH or liver tumorigenesis have not yet been clearly elucidated. Animal models of NAFLD/NASH provide crucial information, not only for elucidating the pathogenesis of NAFLD/NASH, but also for examining therapeutic effects of various agents. A high-fat diet is widely used to produce hepatic steatosis and NASH in experimental animals. Several studies, including our own, have shown that long-term high-fat diet loading, which can induce obesity and insulin resistance, can also induce NASH and liver tumorigenesis in C57BL/6J mice. In this article, we discuss the pathophysiology of and treatment strategies for NAFLD and subsequent NAFLD-related complications such as NASH and liver tumorigenesis, mainly based on lessons learned from mouse models of high-fat diet-induced NAFLD/NASH.     

Adhesion properties of polyurethane pressure-sensitive adhesive

In this study, the adhesion properties of polyurethane (PUR) pressure-sensitive adhesive (PSA) were investigated. The PUR-PSA was prepared by the cross-linking reaction of a urethane polymer consisting of toluene-2,4-diisocyanate and poly(propylene glycol) components using polyisocyanate as a cross-linking agent. The peel strength increased with the cross-linking agent content and exhibited cohesive failure until the maximum value, after which it decreased with interfacial failure. The PUR-PSA exhibited frequency dependence of the storage modulus obtained from dynamic viscoelastic measurements, but did not show dependence of the tack on the rolling rate measured using a rolling cylinder tack test under the experimental conditions used, which is quite different from the acrylic block copolymer/tackifier system. The PUR-PSA showed strong contact time dependence of tack measured by a probe tack test. The tendency was significantly larger than for the acrylic block copolymer/tackifier system. Therefore, the storage modulus increased, whereas the interfacial adhesion seems to be decreased with increase in the rolling rate for this PUR-PSA system. It was estimated that the influence of rolling rate on the interfacial adhesion and the storage modulus was offset, and, as a result, the rolling cylinder tack did not exhibit rate dependency.     

Multiangle Polarimetry of Thermal Emission and Light Scattering by Individual Particles in Airflow

The generalized Kirchhoff's law predicts that the polarization state of thermal emission from an individual small particle depends on the particle shape. We show for the first time experimental evidence confirming this prediction for particles smaller than the wavelength by using a newly developed laser-induced incandescence instrument and a theoretical model that can predict the signals of thermal emission and light scattering for an ellipsoid under the dipole approximation (Rayleigh ellipsoid). We use single-sphere (singlet) and two-sphere clusters (doublet) of polystyrene latex spheres as primary test particles. These are currently available, well-characterized spherical and nonspherical particles, respectively. The polarization states of thermal emission and scattered light of graphite particles smaller than the wavelength show a good agreement with model calculations for plate-like Rayleigh-spheroids, consistent with their plate-like shapes observed by a transmission electron microscope. We propose that the measurement of the polarization state of thermal emission may be applicable to real-time analysis of the shape of light-absorbing particles in air.     

Evaluation of a New Particle Trap in a Laser Desorption Mass Spectrometer for Online Measurement of Aerosol Composition

We have developed a new analyzer for the online measurement of aerosol composition: a particle trap laser desorption mass spectrometer (PT-LDMS). The main components of the instrument include an aerodynamic lens, a particle trap enclosed by a quartz cell, a quadrupole mass spectrometer (QMS), a vacuum chamber incorporating the above components, and a carbon dioxide (CO₂) laser (wavelength 10.6 μm). The aerodynamic lens generates a beam of submicron particles, which is focused on a small area on the particle trap. The particle trap consists of custom-made mesh layers, the structure of which was newly designed using engineering techniques for micro electro mechanical systems (MEMS). A large number of mesh frames are well arranged in the trap, and particles can be efficiently captured after multiple impactions on the frames. The CO₂ laser is used to vaporize aerosol compounds captured on the particle trap. The evolved gas confined within the quartz cell is analyzed using an electron impact ionization (EI) QMS to quantify the chemical composition of the particles. The concept of the PT-LDMS and first evaluation of its performance are presented, specifically focusing on the structure and performance of the particle trap.     

Long-term effect of an enteral diet with a different n-6/n-3 ratio on fatty acid composition and blood parameters in rats

The n-6/n-3 ratio of polyunsaturated fatty acids (PUFAs) in enteral feeding formulas is not considered to be important, because the short-term administration of these formulas has been the norm for postoperative digestive organs. However, the long-term administration of enteral feeding formulas has been increasingly recommended for patients with aging-associated aphagia. This study is aimed at investigating the effect of the long-term administration of an enteral feeding formula containing n-3 polyunsaturated fatty acids (PUFAs) on the fatty acid composition of endogenous phospholipids. Rats, which were initially fed a diet lacking n-3 PUFAs for 2 generations, were subsequently fed an enteral feeding formula containing or lacking n-3 PUFAs for 12 weeks (n = 10). Then, the fatty acid composition of phospholipids in the brain, liver, red blood cells, and plasma of the rats was analyzed. Although the fatty acid composition of neural tissues is suggested to be not affected by diet, the n-6/n-3 ratio of phospholipids in the brains of rats that were fed an enteral feeding formula containing n-3 PUFAs was significantly lower than those of rats that were fed a formula lacking n-3 PUFAs. The enteral feeding formula containing n-3 PUFAs may be effective for the regulation of brain functions and the prevention of atherosclerosis.     

Synthesis of high molecular weight copolymer of styrene and butadiene bearing high 1,4‐cis butadiene unit from copolymerization with CpTiCl3/methylaluminoxane catalyst

Copolymerization of styrene (St) and butadiene (Bd) with CpTiCl₃/methylaluminoxane (MAO) catalyst in the presence or absence of chloranil (CA) was investigated. The CpTiCl₃/MAO catalyst showed a high activity for the copolymerization of St with Bd. The 1,4‐cis contents in the Bd units for the copolymerization of St and Bd with the CpTiCl₃/MAO catalyst was observed, and the 1,4‐cis content was optimum at a MAO/Ti mole ratio of around 225. The effect of the polymerization temperature on the copolymerization was noted, as was the effect of the 1,4‐cis microstructure in the Bd units for the copolymerization of St and Bd. The addition of CA to the CpTiCl₃/MAO catalyst was found to influence the molecular weight of the copolymer. The high weight‐average molecular weight copolymer (M_w = ca. 50 × 10⁴) consisting of mainly a 1,4‐cis microstructure of Bd units (1,4‐cis = 80.0%) was obtained from the copolymerization with the CpTiCl₃/MAO catalyst in the presence of CA (CA/Ti mole ratio = 1) at 0°C. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2942–2946, 2003