“Click Peptide“: pH‐Triggered in Situ Production and Aggregation of Monomer Aβ1–42

Into neutral : We demonstrate the unique features of a pH click peptide based on an O‐acyl isopeptide method. Under acidic conditions, the click peptide remains in a monomeric form. Upon increase of the pH to 7.4, the click peptide is quickly able to convert into Aβ1–42 through an O‐to‐N intramolecular acyl migration. Further study using this pH click peptide would elucidate the pathological role of Aβ1–42 in Alzheimer's disease.

     

Electrochemically Assisted Photocatalysis of Hybrid WO3/TiO2 Films: Effect of the WO3 Structures on Charge Separation Behavior

In this study, the photocatalysis of hybrid WO₃/TiO₂ films with different loadings of WO₃ were investigated with and without potential bias. It was clearly indicated that hybrid WO₃/TiO₂ films show less photo-reactivity under only UV-irradiation, while more effective photocatalysis under potential bias than either TiO₂ or WO₃ by themselves, their photocatalytic performance depending on the loadings of WO₃. In particular, a hybrid WO₃/TiO₂ film involving an amorphous-like WO₃ phase plays a significant role in an enhancement of the electrochemically assisted photocatalysis.     

Removal of phosphate ions with a chemically modified chitosan/metal‐ion complex

The adsorption of metal ions (Mo⁶⁺, Cu²⁺, Fe²⁺, and Fe³⁺) was examined on chemically modified chitosans with a higher fatty acid glycidyl (CGCs), and the adsorption of Cu²⁺ was examined on ethylenediamine tetraacetic acid dianhydride modified CGCs (EDTA‐CGCs) synthesized by the reaction of the CGCs with ethylenediamine tetraacetic acid dianhydride. The adsorption of phosphate ions onto the resulting substrate/metal‐ion complex was measured. Mo⁶⁺ depicted remarkable adsorption toward the CGCs, although all the Mo⁶⁺ was desorbed under the adsorption conditions of the phosphate ions. The other metal ions were adsorbed to some extent on CGCs by chelating to the amino group in the substrate, except for CGC‐1, which had the highest degree of substitution (83.9%). Considerable amounts of Fe²⁺ were adsorbed onto CGCs; however, only a limited number of phosphate ions was adsorbed onto the substrate/metal‐ion complex. As a result, the following adsorbent/metal‐ion complexes gave higher adsorption ability toward phosphate ions: CGC‐4/Cu²⁺, CGC‐4/Fe³⁺, and EDTA‐CGC‐3/Fe³⁺. Where, CGC‐3 is a chemically modified chitosan with the degree of substitution of 26.5 percentage, and CGC‐4 is one with the degree of substitution of 16.0 percentage. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Effect of friction stir processing on microstructure of laser clad cobalt-based alloy

(The microstructural refinement of cobalt-based alloy (Stellite No. 6) by laser cladding and friction stir processing (FSP) was studied. A nanometer-sized microstructure consisting of fine carbide (particle size: 100–200 nm) and a grain (grain size: 150–250 nm) was successfully fabricated by the FSP on the laser clad cobalt-based alloy. The nanostructured cobalt-based alloy (Stellite No. 6) had an extremely high hardness of about 750 HV.     

Preparation of carbon-based transparent and conductive thin films by pyrolysis of silylated graphite oxides

Thin films of silylated graphite oxide were obtained from a chloroform/cyclohexane dispersion of n-hexadecylamine-intercalated silylated graphite oxide by a casting method at a low temperature. Carbon-based thin films were obtained from the pyrolysis of the resulting films under a reduced pressure at 500 °C or higher temperatures. The resulting samples were well adhered to the substrate because of the presence of silicon containing species as a “glue”. The resistivity decreased with an increase in the film thickness or a decrease in the transparency. Based on the data obtained for the samples prepared from graphite with different particle sizes and graphite oxide with different oxygen contents, the conduction of the electrons within each carbon sheet seemed important for large film thickness and conduction through the boundary seemed important when the film thickness was small. A low sheet resistance of 3.7 kΩ/sq for 80% of transmittance was achieved, when graphite oxide with a lower oxygen content was prepared from graphite with smaller particle sizes and the precursor film was heated at 500 °C. At 900 °C, it further decreased to a value of 700 Ω/sq.     

Carbon-coated stainless steel as PEFC bipolar plate material

Stainless steel is quite attractive as bipolar plate material for polymer electrolyte fuel cells (PEFCs). Passive film on stainless steel protects the bulk of it from corrosion. However, passive film is composed of mixed metal oxides and causes a decrease in the interfacial contact resistance (ICR) between the bipolar plate and gas diffusion layer. Low ICR and high corrosion resistance are both required. In order to impart low ICR to stainless steel (SUS304), carbon-coating was prepared by using plasma-assisted chemical vapor deposition. Carbon-coated SUS304 was characterized by Raman spectroscopy and atomic force microscopy. Anodic polarization behavior under PEFC operating conditions (H₂SO₄ solution bubbled with H₂ (anode)/O₂ (cathode) containing 2 ppm HF at 80 °C) was examined. Based on the results of the ICR evaluated before and after anodic polarization, the potential for using carbon-coated SUS304 as bipolar plate material for PEFC was discussed.     

Calculations of heats of formation for nitroaromatics with PM3 and MM2

Abstract

We have attempted to calculate heats of formation (Δ H _f °) for various aromatic nitro compounds with the semi-empirical molecular orbital theory and the molecular mechanics. As the results we may say that PM3, a semi-empirical MO method, and MM2, molecular mechanics, can estimate Δ H _f ° of energetic materials with accuracy enough to use Δ H_f° for energy hazards prediction. In case of aromatic polynitro compounds, both methods may be able to calculate accurate Δ H_f°.     

Linking sanitation and wastewater treatment: from evaluation on the basis of effluent pollutant concentrations to evaluation on the basis of pollutant removal efficiencies

The evaluation of centralised wastewater treatment plants (WWTPs) in planning and management is sometimes based solely on effluent pollutant concentrations or pollutant loads. For sanitation purposes, the effluent pollutant concentrations/loads of WWTPs are important; of course, but from the point of view of wastewater treatment, the pollutant removal performance should also be evaluated. Focussing on low- and middle-income countries, especially those in tropical regions, published kinetics studies on biological WWTPs (such as oxidation ditches and aerated lagoons) are summarised in this paper. In most studies, effluent pollutant concentrations/loads are described as first-order linear functions of influent pollutant concentrations/loads. Therefore, pollutant removal efficiencies can be expressed as first-order linear functions of the reciprocal of influent pollutant concentrations/loads with negative coefficients. This implies that pollutant removal efficiencies increase with influent pollutant concentration/load increases. Based on pollutant removal efficiency functions, biological or ecological WWTPs when operating with small influent pollutant concentrations/loads should change their management to increase influent pollutant concentrations/loads in order to increase pollutant removal efficiencies. It may, however, be possible for technological development in wastewater treatment to overcome this problem.     

Experimental study of hydrogen storage with reaction heat recovery using metal hydride in a totalized hydrogen energy utilization system

Experimental results for hydrogen storage tanks with metal hydrides used for load leveling of electricity in commercial buildings are described. Variability in electricity demand due to air conditioning of commercial buildings necessitates installation of on-site energy storage. Here, we propose a totalized hydrogen energy utilization system (THEUS) as an on-site energy storage system, present feasibility test results for this system with a metal hydride tank, and discuss the energy efficiency of the system. This system uses a water electrolyzer to store electricity energy via hydrogen at night and uses fuel cells to generate power during the day. The system also utilizes the cold heat of reaction heat during the hydrogen desorption process for air conditioning. The storage tank has a shell-like structure and tube heat exchangers and contains 50 kg of metal hydride. Experimental conditions were specifically designed to regulate the pressure and temperature range. Absorption and desorption of 5,400 NL of hydrogen was successfully attained when the absorption rate was 10 NL/min and desorption rate was 6.9 NL/min. A 24-h cycle experiment emulating hydrogen generation at night and power generation during the day revealed that the system achieved a ratio of recovered thermal energy to the entire reaction heat of the hydrogen storage system of 43.2% without heat loss.     

Modification of cleanup methods for dioxin analysis in green leafy vegetables and comparison of packing methods for a multi-layer silica gel column

To determine polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs) and coplanar polychlorinated biphenyls (Co-PCBs) in green leafy vegetables, the cleanup method was modified, and packing methods for a multi-layer silica gel column were compared in food samples. First, the additional cleanup was examined for a mono-ortho PCBs fraction obtained by alumina column chromatography from spinach extract. Small solids such as rough crystals that remained after concentration of the mono-ortho PCBs fraction were identified as long-chain hydrocarbons from leaf epicuticular wax by GC/MS. Cleanup using an activated carbon silica gel column with n-hexane as the washing solvent was effective. Next, multi-layer silica gel columns packed by wet packing and dry packing were compared using komatsuna, salmon and butter as samples. The columns prepared by both methods gave similar values at each isomeric concentration level and showed similar efficiency with favorable recoveries.