Effects of Preform Shear on Tensile Properties of a Woven C/SiC Composite

This article addresses effects of weave defects in an angle‐interlock C‐fiber preform on the tensile properties of the resulting fully processed C‐fiber/SiC‐matrix composite. For this purpose, a preform was intentionally sheared in a controlled manner after weaving. The resulting distortions were quantified by analyzing high‐resolution images of the preform surface after the first step of matrix processing, while the tows were still clearly visible. Comparisons are made of tensile test results on specimens cut from this composite panel and from a pristine panel in select loading orientations. Strain maps obtained by digital image correlation are used to identify local strain variations that are attributable to weave defects. The results are discussed in terms of: (i) the shear‐normal coupling that arises in loading orientations of present interest, and (ii) the geometric effects of tow misalignment on tow continuity along the specimen gauge length. The composite is found to perform in a robust manner, in the sense that the tensile properties are not sensitive to the presence of the defects.     

rGO Sheets/ZnFe2O4 Nanocomposities as an Efficient Electro Catalyst Material for I3−/I− Reaction for High Performance DSSCs

In this paper, Reduced Graphene Oxide (rGO)/ZnFe₂O₄ (rZnF) nanocomposite is synthesized by a simple hydrothermal method and employed as a counter electrode (CE) material for tri-iodide redox reactions in Dye sensitized solar cells (DSSC) to replace the traditional high cost platinum (Pt) CE. X-ray diffraction analysis and High resolution Transmission electron microscopy, clearly indicated the formation of rZnF nanocomposite and also amorphous rGO sheets were smoothly distributed on the surface of ZnFe₂O₄ (ZnF) nanostructure. The rZnF-50 CE shows excellent electro catalytic activity toward I₃^? reduction, which has simultaneously been confirmed by cyclic voltammetry, electrochemical impedance spectroscopy and Tafel polarization measurements. A DSSC developed by rZnF-50 CE (η?=?8.71%) obtained quite higher than the Pt (η?=?8.53%) based CE under the same condition. The superior performances of rZnF-50 CE due to addition of graphene in to Spinel (ZnF) nanostructure results in creation of highly active electrochemical sites, fast electron transport linkage between CE and electrolyte. Thus it’s a promising low cost CE material for DSSCs.

     

Severity of delayed (“secondary”) cerebral energy failure after acute hypoxia-ischemia is related to the time integral of acute ATP depletion

The aim of this study was to reproduce the delayed (secondary) cerebral energy failure previously described in birth-asphyxiated newborn infants and to investigate relationships between primary insult severity and the extent of the delayed energy failure. Phosphorus (³¹P) magnetic resonance spectroscopy (MRS) at 7 T was used to study the brains of 12 newborn piglets during an acute, reversible, cerebral hypoxic-ischemic episode which continued until nucleotide triphosphates (NTP) were depleted. After reperfusion and reoxygenation, spectroscopy was continued for 48 h. High-energy metabolite concentrations returned to near normal levels after the insult, but later they fell as delayed energy failure developed. The time integral of NTP depletion in the primary insult correlated strongly with the minimum [phosphocreatine (PCr)]/[inorganic orthophosphate (P_i)] observed 24–48 h after the insult. (Linear regression analysis gave slope –8.04 h^–1; ordinate intercept=1.23;r=0.92;P<0.0001.) This model is currently being used to investigate the therapeutic potential of various cerebroprotective strategies including hypothermia.     

Effect of Temperatures up to 90°C on the Early Hydration of Portland–Blastfurnace Slag Cements

Isothermal conduction calorimetry has been used to monitor the early hydration of Portland–blastfurnace slag (BFS)-blended cements. Portland:BFS composite cements with ordinary Portland cement replacements from 0 to 90 wt% were studied at curing temperatures from 12° to 90°C. Peak II, principally associated with alite (Ca₃SiO₅) hydration, was accelerated with increasing temperature for all blends. Peak S, associated with BFS hydration, was particularly noticeable at 40° and 60°C. At higher curing temperatures, peak S merged with peak II, indicating thermal activation of BFS. Novel plots of total heat output against percentage replacement show that BFS contributes to the heat of hydration, even at temperatures below its thermal activation.     

Characterization of protein immobilization on nanoporous gold using atomic force microscopy and scanning electron microscopy

Nanoporous gold (NPG), made by dealloying low carat gold alloys, is a relatively new nanomaterial finding application in catalysis, sensing, and as a support for biomolecules. NPG has attracted considerable interest due to its open bicontinuous structure, high surface-to-volume ratio, tunable porosity, chemical stability and biocompatibility. NPG also has the attractive feature of being able to be modified by self-assembled monolayers. Here we use scanning electron microscopy (SEM) and atomic force microscopy (AFM) to characterize a highly efficient approach for protein immobilization on NPG using N-hydroxysuccinimide (NHS) ester functionalized self-assembled monolayers on NPG with pore sizes in the range of tens of nanometres. Comparison of coupling under static versus flow conditions suggests that BSA (Bovine Serum Albumin) and IgG (Immunoglobulin G) can only be immobilized onto the interior surfaces of free standing NPG monoliths with good coverage under flow conditions. AFM is used to examine protein coverage on both the exterior and interior of protein modified NPG. Access to the interior surface of NPG for AFM imaging is achieved using a special procedure for cleaving NPG. AFM is also used to examine BSA immobilized on rough gold surfaces as a comparative study. In principle, the general approach described should be applicable to many enzymes, proteins and protein complexes since both pore sizes and functional groups present on the NPG surfaces are controllable.     

A comparative study of the emotional assessment of automotive exterior colors in Asia

This article compares color assessments of automotive exteriors at four locations in China, Thailand and Japan. This study employed painted panels of twelve colors, thirty sensory words and fifteen pairs of emotion variables. It also used reference figures of nine cars that included four styling categories, namely sedans, compacts, sport utility vehicles and sports cars. The results of like-dislike tests revealed that basic automotive exterior colors, such as black, white and red, were highly preferred across locations. However, geographical differences are apparent in the preference for some non-basic colors. To elucidate these geographical differences, a Chi-square test and principal component analysis were performed on the data on emotion variables. The results revealed both similarities and differences in color preferences among the four locations. Color preferences were similar in Hong Kong and Shanghai when simply evaluated by color samples. However, similar preferences for automotive exterior colors were observed in Hong Kong, Kyoto and Bangkok, but not in Shanghai. These results suggest that there is fluctuation in the emotion evoked by a color when the color is considered in the context of automotive exteriors. Therefore, this study indicates that automotive sales can be secured in the global marketplace by creating a single palette of exterior colors based on similar color preferences across countries. However, these results also indicate that preparing market-specific automotive-color line-ups can be an effective marketing strategy.     

Pyro-catalytic deoxgenated bio-oil from palm oil empty fruit bunch and fronds with boric oxide in a fixed-bed reactor

The catalytic effect of boric oxide on the pyrolysis of empty palm oil fruit bunch (EFB) and oil palm fronds (OPF) in a fixed-bed reactor at 400 °C was investigated. Boric oxide was found to selectively reduce 50-80% of the hydroxyl and methoxy groups in both water soluble (WS) and non water soluble (NWS) fractions of the oil. The increase in water and char yield suggested that pyro-catalysis of boric oxide enhanced the cleavage of C-O bonds in the biomass polymers and the capability to retain the inherent oxygen of the biomass in the solid product. This allows organic compounds with less oxygen substitution to become volatile and condenses as bio-oil. A mechanism for pyrolysis of boric oxide with biomass showing the hydroxyl removal pathway is proposed in this study.     

Assessing the catalytic effect of coal ash constituents on the CO2 gasification rate of high ash, South African coal

The catalytic effect of inorganic species, within the ash, on the CO₂ gasification of three South African coals containing similar carbon-structural properties (elemental, structural and petrographical properties) was assessed. The reactivity of the coals with a particle size between 150 and 250 μm was determined in a thermo gravimetric analyser. The reactivity was measured at temperatures between 900 and 1000 °C, pressures between 1 and 10 bar, and fractions of CO₂ between 10 and 30%. For the selected coals, the reactivity decreased with ash content, and was found to be dependent on the composition of the ash. Specifically, the reactivity increased with calcium and magnesium content and alkali index.     

Efficient H-NMR Quantitation and Investigation of N-Acetyl-d-glucosamine (GlcNAc) and N,N'-Diacetylchitobiose (GlcNAc)(2) from Chitin

A quantitative determination method of N-acetyl-d-glucosamine (GlcNAc) and N,N'-diacetylchitobiose (GlcNAc)(2) is proposed using a proton nuclear magnetic resonance experiment. N-acetyl groups of GlcNAc and (GlcNAc)(2) are chosen as target signals, and the deconvolution technique is used to determine the concentration of the corresponding compound. Compared to the HPLC method, (1)H-NMR spectroscopy is simple and fast. The method can be used for the analysis of chitin hydrolyzed products with real-time analysis, and for quantifying the content of products using internal standards without calibration curves. This method can be used to quickly evaluate chitinase activity. The temperature dependence of (1)H-NMR spectra (VT-NMR) is studied to monitor the chemical shift variation of acetyl peak. The acetyl groups of products are involved in intramolecular H-bonding with the OH group on anomeric sites. The rotation of the acetyl group is closely related to the intramolecular hydrogen bonding pattern, as suggested by the theoretical data (molecular modeling).