Acoustic Emission Studies of Alumina-13% Titania Free-Standing Forms during Four-Point Bend Tests

Free-standing alumina-13% titania samples were manufactured with a water-stabilized plasma spray gun to a thickness of ∼5 mm. A thin layer of aluminum was arc sprayed prior to depositing the thick coating and etched away using hydrochloric acid. The so-obtained free-standing plate was cut into four-point-bend-test specimens with dimensions of ∼5 mm × 5 mm × 50 mm. The as-sprayed material consisted of a supersaturated solid solution, where titania was frozen inside the alumina matrix. Heat treatment was performed at 1450°C for 24 h and then at 1100°C for another 24 h. After heat treatment, titania precipitates were observed. The major phases of the as-sprayed and heat-treated samples were γ- and α-alumina, respectively. The porosity was ∼10% for as-sprayed samples; this value was reduced to ∼3% after heat treatment. Four-point bend tests were performed on the as-sprayed and heat-treated specimens in cross-section and in-plane directions. An acoustic emission technique was used to examine the cracking during the tests in situ. Microcracking prior to failure was observed for as-sprayed samples that were tested in the cross-section direction. However, when tested in the in-plane direction, catastrophic failure with less evidence of microcracking occurred. For heat-treated specimens, microcracks were usually observed when tests were performed in either of the orientations. Energy and amplitude distributions for each testing condition were examined. These distributions changed after heat treatment; however, no significant differences were distinguished when tests were performed in the cross-section or in-plane directions.     

Application of citric acid as natural adhesive for wood

The development of natural adhesives derived from nonfossil resources is very important for the future. Besides, it is desirable to be safe adhesives without using harmful chemical substances. In this study, application of citric acid as a natural adhesive was investigated. Citric acid powder and bark powder obtained from Acacia mangium were used as raw materials. Citric acid powder was mixed with the bark powder, and the resulting powder mixture was poured into a metal mold. The mold was hot‐pressed at 180°C and 4 MPa for 10 min, and a bark molding was then obtained. The specific modulus of rupture and modulus of elasticity values of the molding containing 20 wt % citric acid were 18.1 MPa and 4.9 GPa, respectively. The molding did not decompose during a repeated boiling treatment. To clarify the effect of tannin on the adhesiveness of molding, bark was separated into tannin and residue. The molding was not obtained while using the tannin due to the marked fluidity, whereas it was obtained while using the residue, the same as while using the bark. It was considered that components other than tannin contributed to the adhesiveness. Based on the results of Fourier transform infrared spectra, the formation of ester linkages between carboxyl groups derived from citric acid and hydroxyl groups in the bark was confirmed. Accordingly, citric acid brought an adhesion by chemical bonding, and it could be used as a safe natural adhesive. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effects of Amino Acids and Peptide on Lipid Oxidation in Emulsion Systems

We investigated the effects of amino acids and peptide on lipid oxidation in emulsion systems. For comparative purposes, we also tested the antioxidant activity of ferulic acid, a typical phenolic antioxidant. Histidine and cysteine retarded lipid oxidation (the amount of thiobarbituric acid [TBA]-reactive substances reached approximately 13 and 18 μM after 7 days, respectively), whereas arginine, methionine, and tryptophan did not inhibit the progression of oxidation. Soy peptide also inhibited lipid oxidation. Ferulic acid was found to be the most effective suppressor of lipid oxidation (TBA-reactive substances were suppressed to <3 μM over 7 days). The antioxidant activities of soy peptide and ferulic acid were related to the purity of the emulsifier used. The radical scavenging activities of soy peptide and ferulic acid were closely related to their inhibitory effects on lipid oxidation. However, this was not the case for amino acids. Decreases in the turbidity of emulsions were closely related to increases in TBA values.     

Influence of Cu metal on the domain structure and carrier mobility in single-layer graphene

We demonstrate that domain structure of single-layer graphene grown by ambient pressure chemical vapor deposition is strongly dependent on the crystallinity of the Cu catalyst. Low energy electron microscopy analysis reveals that graphene grown using a Cu foil gives small and mis-oriented graphene domains with a number of domain boundaries. On the other hand, no apparent domain boundaries are observed in graphene grown over a heteroepitaxial Cu(111) film deposited on sapphire due to unified orientation of graphene hexagons. The difference in the domain structures is correlated with the difference in the crystal plane and grain structure of the Cu metal. The graphene film grown on the heteroepitaxial Cu film exhibits much higher carrier mobility than that grown on the Cu foil.     

Non‐Enzymatic Geometry‐Selective Acylation of Tri‐ and Tetrasubstituted α,α′‐Alkenediols

A highly geometry‐selective organocatalytic acylation of tri‐ and tetra‐substituted 2‐alkylidene‐1,3‐propanediols has been developed. The highly E‐selective acylation of various tetrasubstituted 2‐alkylidene‐1,3‐propanediols was achieved in 96 to >99% selectivity for the first time by a non‐enzymatic protocol.     

Molecular mechanisms of epigenetic variation in plants

Natural variation is defined as the phenotypic variation caused by spontaneous mutations. In general, mutations are associated with changes of nucleotide sequence, and many mutations in genes that can cause changes in plant development have been identified. Epigenetic change, which does not involve alteration to the nucleotide sequence, can also cause changes in gene activity by changing the structure of chromatin through DNA methylation or histone modifications. Now there is evidence based on induced or spontaneous mutants that epigenetic changes can cause altering plant phenotypes. Epigenetic changes have occurred frequently in plants, and some are heritable or metastable causing variation in epigenetic status within or between species. Therefore, heritable epigenetic variation as well as genetic variation has the potential to drive natural variation.     

The Potential Role of Hepatocyte Growth Factor in Degenerative Disorders of the Synovial Joint and Spine

This paper aims to provide a comprehensive review of the changing role of hepatocyte growth factor (HGF) signaling in the healthy and diseased synovial joint and spine. HGF is a multifunctional growth factor that, like its specific receptor c-Met, is widely expressed in several bone and joint tissues. HGF has profound effects on cell survival and proliferation, matrix metabolism, inflammatory response, and neurotrophic action. HGF plays an important role in normal bone and cartilage turnover. Changes in HGF/c-Met have also been linked to pathophysiological changes in degenerative joint diseases, such as osteoarthritis (OA) and intervertebral disc degeneration (IDD). A therapeutic role of HGF has been proposed in the regeneration of osteoarticular tissues. HGF also influences bone remodeling and peripheral nerve activity. Studies aimed at elucidating the changing role of HGF/c-Met signaling in OA and IDD at different pathophysiological stages, and their specific molecular mechanisms are needed. Such studies will contribute to safe and effective HGF/c-Met signaling-based treatments for OA and IDD.     

Catalyst Design of Pt-Modified Ni/Al2O3 Catalyst with Flat Temperature Profile in Methane Reforming with CO2 and O2

Pt(0.3)/Ni(10)/Al₂O₃, prepared by a sequential impregnation method, exhibited a more excellent performance in methane reforming with CO₂ and O₂ in terms of the catalytic activity and the temperature profile of the catalyst bed than Pt(0.3) + Ni(10)/Al₂O₃ prepared by a coimpregnation method, Ni(10)/Al₂O₃, Pt(0.3)/Al₂O₃, and Pt(10)/Al₂O₃. It is thought that this is because the surface Pt atoms on Ni catalyst can contribute to the enhancement of the catalyst reducibility.     

New class of cellulose fiber spun from the novel solution of cellulose by wet spinning method

A novel cellulose solution, prepared by dissolving an alkali-soluble cellulose, which was obtained by the steam explosion treatment on almost pure natural cellulose (soft wood pulp), into the aqueous sodium hydroxide solution with specific concentration (9.1 wt %) was employed for the first time to prepare a new class of multifilament-type cellulose fiber. For this purpose a wet spinning system with acid coagulation bath was applied. The mechanical properties and structural characteristics of the resulting cellulose fibers were compared with those of regenerated cellulose fibers such as viscose rayon and cuprammonium rayon commercially available. X-ray analysis shows that the new cellulose fiber is crystallographically cellulose II, and its crystallinity is higher but its crystalline orientation is slightly lower than those of other commercial regenerated fibers. The degree of breakdown of intramolecular hydrogen bond at C₃[X_am(C₃)] of the cellulose fiber, as determined by solid-state cross-polarization magic-angle sample spinning (CP/MAS) ¹³C NMR, is much lower than other, and the NMR spectra of its dry and wet state were significantly different from each other, indicating that cellulose molecules in the new cellulose fiber are quite mobile when wet. This phenomenon has not been reported for so-called regenerated cellulose fibers.     

Sintering of Ceria-Doped Tetragonal Zirconia Crystallized in Organic Solvents, Water, and Air

Amorphous CeO₂–ZrO₂ gels were prepared by coprecipitation in ammonia solutions. The onset of crystallization of the gels, from calcining in air, was 420°C, while 200° to 250°C in the presence of water and organic solvents such as methanol and ethanol. The sintering behaviors of CeO₂–ZrO₂ powders were sensitive to the crystallizing conditions, since hard agglomerates formed when the precipitated gels were crystallized by normal calcination in air, whereas soft agglomerates formed when they were crystallized in water or organic solvents. CeO₂–ZrO₂ powders crystallized in methanol and water at 250°C were sintered to full theoretical density at 1150° and 1400°C, respectively, whereas that crystallized by calcination in air at 450°C was sintered to only 95.2% of theoretical density, even at 1500°C.