Additive Effects of Solid Paraffins on Mechanical Properties of High-Density Polyethylene.

In this work, two types of solid paraffins (i.e., linear and branched) were added to high-density polyethylene (HDPE) to investigate their effects on the dynamic viscoelasticity and tensile properties of HDPE. The linear and branched paraffins exhibited high and low crystallizability, respectively. The spherulitic structure and crystalline lattice of HDPE are almost independent of the addition of these solid paraffins. The linear paraffin in the HDPE blends exhibited a melting point at 70 °C in addition to the melting point of HDPE, whereas the branched paraffins showed no melting point in the HDPE blend. Furthermore, the dynamic mechanical spectra of the HDPE/paraffin blends exhibited a novel relaxation between -50 °C and 0 °C, which was absent in HDPE. Adding linear paraffin toughened the stress-strain behavior of HDPE by forming crystallized domains in the HDPE matrix. In contrast, branched paraffins with lower crystallizability compared to linear paraffin softened the stress-strain behavior of HDPE by incorporating them into its amorphous layer. The mechanical properties of polyethylene-based polymeric materials were found to be controlled by selectively adding solid paraffins with different structural architectures and crystallinities.

Validation of a Method for Quantification of Lutein in Spinach Using High-Performance Liquid Chromatography: Interlaboratory Study.

BACKGROUND: Lutein is gaining attention as a strong antioxidant contained in foods. It accumulates in the human blood and retina, and is considered to play an important role in the body, especially in the eyes. OBJECTIVE: A method to determine the lutein content of raw spinach (Spinacia oleracea L.) was developed with the aim of its enactment as a Japanese agricultural standard (JAS) measurement method for components beneficial to human health. METHODS: An interlaboratory study was conducted to evaluate an analytical method for the determination of lutein in spinach. The detection limit and quantification limit of lutein for this method were 0.2 and 0.7 mg/kg, respectively. Twelve participating laboratories independently analyzed test samples (five pairs of blind duplicates) using high-performance liquid chromatography (HPLC). RESULTS: After removal of a few outliers, the repeatability relative standard deviation (RSDr), reproducibility (RSDR), and predicted RSDR of the evaluated method were 3.4-7.5, 4.6-13, and 7.5-8.5%, respectively, in a concentration range from 64.9-150 mg/kg. CONCLUSIONS: The HorRat values (RSDR/predicted RSDR) of the lutein concentration were calculated to be 0.61-1.6. HIGHLIGHTS: The study results indicate the acceptable precision of this method.

Electrochemical carboxylation of alpha-chloroethylbenzene in ionic liquids compressed with carbon dioxide.

Electrochemical carboxylation is conducted in ionic liquids compressed with carbon dioxide. It is found that the current efficiency increases with temperature and pressure. The diffusion coefficient of the substrate, which is obtained from the electrochemical measurements, also remarkably increases with temperature and pressure. The increase of the current efficiency is mainly explained by improvement in the mass transfer, and the promotion of the electrochemical carboxylation in the ionic liquid is achieved by pressurizing the carbon dioxide moderately.

Reaction between diiodide anion radicals in ionic liquids.

Photodetachment of electrons from iodide ions produced diiodide anion radicals in ionic liquids containing ammonium, pyrrolidinium, and piperidinium cations. The rates of reaction between diiodide anion radicals in molecular solvents such as H2O, methanol, and ethanol could be estimated by the Debye-Smoluchowski equation, which accounts for electrostatic interactions using dielectric constants for the molecular solvents. In contrast, the rates of reaction between diiodide anion radicals in the ionic liquids were close to the diffusion-limited rates for the neutral molecules, suggesting that electrostatic repulsion between the diiodide anion radicals is weakened by Coulombic shielding in the ionic liquids.

Melting point depression of ionic liquids confined in nanospaces.

A new physical method was proposed to control the liquid properties of room temperature ionic liquids (RT-ILs) in combination with nanoporous materials; the melting point of ILs confined in nanopores remarkably decreases in proportion to the inverse of the pore size.

Temperature dependence of local density augmentation for acetophenone N,N,N',N'-tetramethylbenzidine exciplex in supercritical water.

Local density augmentation around exciplex between acetophenone and N,N,N',N'-tetramethylbenzidine in supercritical water was measured by observing the peak shift of transient absorption spectrum at temperatures from 380 to 410 degrees C and at pressures from 6 to 37 MPa. Large local density augmentation was observed at lower solvent densities. Local density augmentation was evaluated by the excess density, which was defined as the difference between local density and bulk density, and the density enhancement factor, which was defined by the ratio of the local density to the bulk density. The number of solvating molecules was estimated with a Langmuir adsorption model. The excess density was found to exhibit a maximum at approximately 0.15 g cm(-3), which decreased with increasing temperature. The density enhancement factor was found to decrease with increasing temperature; however, its value was much greater than unity at 410 degrees C, which provides evidence that exciplex-water interactions still exist at these conditions. The temperature dependence of local density augmentation around the exciplex in supercritical water was comparable with that in supercritical carbon dioxide, which suggests that the ratios of the solute-solvent and solvent-solvent interactions are comparable between these two systems.

Solution structures of 1-butyl-3-methylimidazolium hexafluorophosphate ionic liquid saturated with CO2: Experimental evidence of specific anion-CO2 interaction.

X-ray diffraction measurements for 1-butyl-3-methylimidazolium hexafluorophosphate ionic liquid ([BMIM][PF6])-CO2 systems were carried out at high pressures with a newly developed polymer cell. The intermolecular distribution functions (g(inter)(r)) were obtained at 25 degrees C for neat [BMIM][PF6] and its solutions saturated with CO2 at 4 and 15 MPa, where the mole fractions (x) of CO2 correspond to 0.5 and 0.7, respectively. In g(inter)(r) for x = 0.5, two peaks appeared at around 2.8 and 3.2 A. These two peaks in g(inter)(r) appreciably increased for x = 0.7; moreover, there was another peak observed at approximately 3.8 A. Only assuming the correlations between CO2 and [PF6]-, it is reasonably determined that the nearest-neighbor P([PF6]-). . .C(CO2) distances are 3.57 and 3.59 A with the coordination numbers being 1.8 and 4.0 for x = 0.5 and 0.7, respectively. It is concluded that CO2 molecules are preferentially solvated to the [PF6]- anion.