Dietary exposure to acrylamide in a group of Japanese adults based on 24-hour duplicate diet samples

Acrylamide is a probable human carcinogen and known human neurotoxin that can be generated in food through heating. Using a mathematical modelling approach, our previous study estimated long-term average dietary exposure to acrylamide in the Japanese people; however, the validity of these estimates remained unknown. Here, we aimed to obtain a more accurate estimate of acrylamide exposure that would reflect the usual practice of heat processing and consumption of foods in the population. We collected duplicate diet samples and dietary records during 24 h from a group of Japanese adults. A total of 110 duplicate diet samples were analysed for acrylamide by LC-MS/MS. Data from individual dietary records were used to examine the association between dietary acrylamide exposure and consumption of selected food groups (e.g., coffee, tea, confectioneries, and vegetables prepared at high temperature [deep-frying, stir-frying, sautéing, and baking]). Of the 110 homogenised diet samples, 108 contained detectable levels of acrylamide. Dietary exposure to acrylamide ranged from 8 to 1582 ng/kg body weight (bw)/day, with the mean value of 215 ng/kg-bw/day and median value of 143 ng/kg-bw/day. This mean value was higher than the value we previously estimated for Japanese adults using a mathematical approach. Multiple linear regression analysis showed log dietary acrylamide exposure was significantly associated with consumption of coffee and vegetables prepared at high temperature during 24-hr of sampling (adj. R² = 0.250, p < 0.001). We revealed significant difference in dietary acrylamide exposure between participants who had coffee and vegetables prepared at high temperature (median, 169 ng/kg-bw/day; range, 35–1224 ng/kg-bw/day, n = 42) and those who had none of them (median, 75 ng/kg-bw/day; range, 8–311 ng/kg-bw/day, n = 15) (Steel-Dwass test, p < 0.05).     

Selective vapor phase hydroformylation of ethylene over cluster-derived cobalt catalyst

Vapor phase hydroformylation of ethylene was studied with silica-supported metal catalysts. A cobalt metal catalyst derived from Co₂(CO)₈ gave propanal and its derivatives in as high selectivity of about 36% as Rh/SiO₂ catalyst under the reaction conditions of 1.1 MPa of a gas-mixture of ArCOC₂H₄H₂ = 1333 at 423–503 K. On the other hand, conventional cobalt catalysts derived from cobalt nitrate, chloride, or acetate, and other noble metal catalysts (Pd/SiO₂ and Ir/SiO₂) produced mainly ethane.     

Color and Vanadium Valency in V-Doped ZrO2

The distribution and chemical states of vanadium in V-doped ZrO₂ were studied to clarify the origin of the color of vanadium-zirconium yellow pigment in comparison with vanadium-tin yellow pigment. ESCA data and measurements of lattice constants of V-doped ZrO₂ revealed that vanadium was dissolved mainly as V⁴⁺ substituting for Zr in ZrO₂ lattice, and its solubility limit was 0.5 wt% as V₂O₅. It was found that the yellow color of vanadium-zirconium yellow was produced predominantly by the dissolved vanadium and that the contribution of vanadium oxide on ZrO₂ grains to the yellow color was about 1/30 of that of the dissolved vanadium when compared on the basis of equimolar quantity of vanadium. Most of the undissolved vanadium oxide was in an amorphous or a poorly crystallized state.     

Synthetic Molecular Gear Based on Double-Decker Porphyrin Complexes

New rotary molecular machines (1 and 2) were synthetically constructed from two distinct porphyrin-based rotors, a cerium(IV) bis(porphyrinate)s double-decker (CeDD) and a porphyrinatorhodium(III)-based rotor. These rotors are adjacently mounted on rotational axes aligned to near vertical as resembling the bevel-gear-shaped structure. Structural study using NMR analysis reveals that these distinct rotors are connected through a coordination bond between rhodium(III) and a pyridyl group. At temperature from 193 to 393 K, each rotor represents rotational motion driven by heat fluctuation without decomposition into the corresponding precursors in dichloromethane-d ₂ and tetrachloroethane-d ₄. Importantly, the mechanical interaction between the teeth of these rotors is strongly dependent on the central metal atom in a DD rotor and the teeth structure in a porphyrinatorhodium(III)-based rotor. Understanding such relationship between the chemical structures and mechanical interaction is of importance for generating cooperative motion in the hybrid machinery system.     

Runoff Analysis for a Small Watershed of Tono Area Japan by Back Propagation Artificial Neural Network with Seasonal Data

The rainfall runoff (R-R) process was studied for two small sub-basins having different sizes in a mountainous catchment of Tono area Japan. The runoff and other meterological data have been collected in this catchment for the last 14 years. The major objective of this study was to construct numerical models for these sub-basins to predict runoff after 1/2 and 1 h. The effects of season and the size of the catchment on R-R process were also investigated. The hydrogeological conditions of the catchment were studied prior to the analyses. The data obtained for summer (rainy) and winter (dry) seasons were treated separately in order to study the seasonal effects on the model development. The back propagation artificial neural network technique (BPANN) and the multivariate autoregressive and moving average models (ARMA) were adopted for the analysis. It was found that for very small catchments the seasonal effects are dominant and therefore separate models should be developed for each season to obtain better forecasting estimates. It was also found that the predictions by BPANN models were better than multivariate ARMA models for intense rains having complex R-R relationships in summer. On the other hand, both the modelling techniques yielded almost similar results for smaller rains in winter. It was also found clearly that the accuracy of prediction decreased with the increase of the time period for prediction.     

Geometry Dependence of Magnetization Reversal in Nanocomposite Alloys

The geometrical optimization of aligned hard-soft permanent-magnet nanocomposites is investigated by model calculations. Considered criteria are the shapes of the soft and c-axis-aligned hard phases, the packing fraction of the soft phase, and magnetostatic interactions. Taking into account that the energy product is enhanced via the volume fraction of the soft phase, subject to maintaining coercivity, we find that the best structures are soft-magnetic cubes as well as long rods with a square cross section. Comparing embedded soft cubes with embedded soft spheres of the same size, our nucleation-field analysis shows that the volume fraction of the soft phase is enhanced by 91%, with a coercivity reduction of only 25%. Magnetostatic interactions often but not always deteriorate the permanent-magnet performance, as exemplified by the example of MnBi:FeCo bilayers and multilayers.     

Thermal decomposition of cellulose/synthetic polymer blends containing grafted products. V. Cellulose/polystyrene blends

Homogeneous grafting of styrene onto cellulose was carried out in a dimethylacetamide/lithium chloride solvent system. The grafted products were added to cellulose/polystyrene (PS) blends as compatibilizers. The thermal decomposition behavior of the blends was investigated by thermogravimetry. The thermal stability of the blends decreased with an increase in grafted product content. The crystallinity of the blends decreased with grafted product content. The microphase‐separated structures of the blends became finer with grafted product content. The glass transition temperatures for cellulose and PS in the blends were lowered with grafted product content. Differences in thermal decomposition behavior of the blends were correlated with compatibility. Thermogravimetry was effective for compatibility estimation in cellulose/PS blends containing grafted products. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Silver vanadium phosphorous oxide, Ag2VO2PO4: Chimie douce preparation and resulting lithium cell electrochemistry

Recently, we have shown silver vanadium phosphorous oxide (Ag₂VO₂PO₄, SVPO) to be a promising cathode material for lithium based batteries. Whereas the first reported preparation of SVPO employed an elevated pressure, hydrothermal approach, we report herein a novel ambient pressure synthesis method to prepare SVPO, where our chimie douce preparation is readily scalable and provides material with a smaller, more consistent particle size and higher surface area relative to SVPO prepared via the hydrothermal method. Lithium electrochemical cells utilizing SVPO cathodes made by our new process show improved power capability under constant current and pulse conditions over cells containing cathode from SVPO prepared via the hydrothermal method.     

Pd20Pt20Cu20Ni20P20 high-entropy alloy as a bulk metallic glass in the centimeter

A Pd₂₀Pt₂₀Cu₂₀Ni₂₀P₂₀ bulk metallic glass (BMG) with a high-entropy (HE) alloy composition and a maximum diameter of 10 mm was fabricated by fluxed water quenching. The system and composition of the Pd₂₀Pt₂₀Cu₂₀Ni₂₀P₂₀ alloy were determined from a prototype ternary Pd₄₀Ni₄₀P₂₀ BMG in accordance with two strategic alloy designs of (1) HE alloy defined by an equi-atomic alloy with five or more elements and (2) exchangeability of the constituent elements with a similar chemical nature in the periodic table. Pd₂₀Pt₂₀Cu₂₀Ni₂₀P₂₀ HE-BMG had a supercooled liquid range of 65 K and a reduced glass transition temperature of 0.71. Successful formation of Pd₂₀Pt₂₀Cu₂₀Ni₂₀P₂₀ HE-BMG is significant to develop new alloys for HE alloys and BMGs.