Semi-annual cycle of sea-surface temperature in the East/Japan Sea and cooling process

Semi-annual cycles of the sea-surface temperature (SST) in the East/Japan Sea (EJS) and their forcings were examined by analysing National Oceanic and Atmospheric Administration/Advanced Very-High-Resolution Radiometer data, scatterometer wind vectors, and heat flux data. The semi-annual cycle contributed to the total variance of the SST by 8% and amounted to 25% of the amplitudes of the annual SST cycle, particularly in the Tatarskiy Strait and along the continental shelf off Russia. The lowest phase, corresponding to the minimum SST, occurred during early November and 6 months earlier in May or June depending on the position. The forcings of the semi-annual cycle were not semi-annual but substantially annual with a lag of 6 months, which gave rise to SST cooling in spring and autumn. Our analyses illustrated that SST cooling in autumn was caused by direct, local atmospheric wind forcings, whereas the cooling with large amplitudes of the semi-annual cycle in spring was caused by the non-local, remotely forced cold water advection of the Liman Current associated with sea-ice melting in the Tatarskiy Strait. The phase lag of 1–2 months between the complete melting of the sea ice in the Tatarskiy Strait and the surface cooling along the Russian continental shelf was related to the advection of cold water from sea ice in the form of the Liman Cold Current. The semi-annual cycle also resulted from asymmetry of the time series of the SST due to a long cold winter and a short warm summer. To understand how SST curves are distorted and asymmetric, we suggested two mathematical parameters of kurtosis and skewness. In addition, we suggest that the ratio of the semi-annual amplitude to the annual amplitude of SST harmonics can be used as a typical indicator of the asymmetry in year-to-year SST variations.     

The use of non–physical standards in colour communication and matching

As a result of developments in spectrophotometry, together with improved accuracy in computer colour matching and laboratory dyeing, non–physical standards (reflectance data) can now be used for the successful communication, matching and quality control of colour. In colour palette generation, ‘matching by numbers’ has become a reality.     

Microstructural Evidence for Diffusion-Driven Tetragonal-to-Orthorhombic Phase Transformation in Y-Ba-Cu-O Superconductor

Microstructures of Y-Ba-Cu-O superconductor were observed using a polarized microscope. Orthorhombic and tetragonal phases were easily distinguished by the optical etching with cross-polarized light. In the specimen cooled rapidly in oxygen, it was possible to see the path of oxygen diffusion by observing the variation of the twin concentration. At the boundary between transformed and untransformed materials, evidence for diffusion-driven transformation could be clearly seen.     

Adsorption and desorption characteristics of 2-methyl-4-chlorophenoxyacetic acid onto activated carbon

Adsorption and desorption characteristics of the 2-methyl-4-chlorophenoxyacetic acid (MCPA) from aqueous solution onto the activated carbon (GAC, F-400) were studied. Adsorption equilibrium capacities of the MCPA increased with decreasing pH and temperature of the solution. Adsorption equilibrium of the MCPA could be represented by the Sips equation. The internal diffusion coefficients were determined by comparing the experimental concentration decay curves with those predicted from surface diffusion model and pore diffusion model. The adsorption model based on the linear driving force approximation (LDFA) was used for simulating the adsorption behavior of the MCPA in a fixed bed. Over ninety five percent desorption of the MCPA could be obtained using distilled water.     

Monodisperse polymer/metal composite particles by electroless chemical deposition: Effect of surface functionality of polymer particles

Micron‐sized polymer particles were coated with layers of nickel compounds by plating electrolessly in the presence of aqueous solutions of nickel chloride, sodium hypophosphite, sodium citrate, and ammonium chloride at elevated temperature. The uniform functional polymer particle could be obtained by seeded polymerization. To investigate the effect of surface functionality on the conditions for nickel deposition, the polymer particle was functionalized with the thiol group. From morphological observation, it was found that the mode of nickel deposition was greatly dependent on the surface functionality of the polymer particle. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 420–424, 2003     

Preparation of nano-sized silicon carbide powder using thermal plasma

Nano-sized silicon carbide (SiC) powder was prepared by thermal plasma process using silicon tetrachloride (SiCl₄) and methane (CH₄). The synthesized powder was characterized by X-ray diffraction pattern, scanning electron microscopy, transmission electron microscopy, FT-IR spectroscopy and particle size analyzer. The powder was dominated by β-SiC including some of α-SiC and free carbon species. The quality of the powder was varied with process conditions such as the molar ratio of H/Si and C/Si, and collecting positions. It was known that the conversion to SiC was mainly affected by the addition of hydrogen gas because it promoted the decomposition and reduction of SiCL. CH₄ was easily decomposed to carbon species for the formation of SiC as well as removal of impure oxygen, but excessive carbon suppressed the formation of crystalline SiC and resulted in the solid carbon contamination. The optimum ratio of H/Si was approx. 26 and that of C/Si was 1.1. For collecting positions, the powder collected at the vessel and filter was preferable to that at the reaction tube. The average size of the powder synthesized was estimated to be below 100 nm and uniform in distribution.     

AMMONIA CATALYZED ORGANOSOLV DELIGNIFICATION OF POPLAR

A parametric investigation of NH₄OH catalyzed solvent delignification of poplar was conducted to define pretreatment conditions which would yield an optimal separation of the biomass components and an enzymatic susceptible solid carbohydrate phase. Delignification parameters of interest included concentration of NH₄OH, time and temperature of the reaction, and type of solvent. The addition of 0.82 M NH₄OH to the delignification liquor increased lignin removal and decreased carbohydrate degradation, but increasing NH₄OH concentration had no additional effect. At lower reaction temperatures, the extent of delignification increased with reaction time; at higher temperatures, a “relignification” of the pretreated wood was observed. The delignification and hemicellulose solubilization were modelled and rate constants reported. No major difference between three potential pulping solvents—ethanol, butanol, phenol—was observed. The enzymatic susceptibility of pretreated wood samples was approximately 6-fold greater than that of the untreated poplar. UV absorbance was used to qualitatively characterize the soiubilized lignins.     

Concentration of tocopherols from soybean sludge by supercritical carbon dioxide

A supercritical fluid extraction method has been applied to test the feasibility of tocopherol concentration from soybean sludge with carbon dioxide at temperatures and pressures ranging from 35 to 70°C and 200 to 400 bar, respectively. The supercritical solubility of the esterified soybean sludge was over 4–6 times greater than that of the original soybean sludge. By a simple batch-type one-stage method the tocopherols in the esterified soybean sludge could be concentrated up to 40 wt%. The overall results of the present study show that soybean sludge initially containing about 13–14 wt% tocopherols may require a countercurrent multistage column to be highly and effectively concentrated.     

High catalytic activity of PdOx/MnO2 for CO oxidation and importance of oxidation state of Mn

PdO_x/MnO₂ has been examined as a catalyst for CO oxidation using a conventional flow reactor at reaction temperatures between 50 and 150°C. In the reaction conditions of GHSV (gashourlyspacevelocity) of 1.22 × 10⁵/h and CO concentration of 2000 ppm, PdO_x/MnO₂ showed higher catalytic activity compared with PdO_x/Mn₂O₃, which had been previously reported as an effective catalyst due to the cooperative action of Pd and Mn₂O₃ for this reaction. The reason for higher activity of PdO_x/MnO₂ than PdO_x/Mn₂O₃ has been investigated using TPR (temperatureprogrammed reduction) and XPS studies. TPR showed that PdO_x/MnO₂ could be reduced by CO at much lower temperature than PdO_x/Mn₂O₃. During the experiment of reduction and oxidation, XPS showed that the valence of Mn in the PdO_x/MnO₂ was between 4+ and 3+, which is higher than that of Mn in the PdO_x/Mn₂O₃ catalyst of which the valence has been reported to be between 3+ and 2+. It is known that in this catalyst system the support supplies oxygen onto Pd, where the oxidation occurs with adsorbed CO, and the ability of the support to provide oxygen improves the performance of the catalyst. Therefore, it was concluded that the readiness of MnO₂ to be reduced with maintaining a higher oxidation state showed higher CO oxidation activity than Mn₂O₃ as support for PdO_x.     

Effect of extrusion temperature on elongational flow behavior of PVC melt

The effect of the sample extrusion temperature between 160° and 180°C on the elongational flow properties of a low molecular weight suspension PVC (unplasticized) has been studied with the Rheometrics Extensional Rheometer. The results of both the tensile creep measurements at a constant stress of 24 KPa and the stretching experiment at a constant strain rate of 0.01 sec^?1 indicated the existence of a rheological transition at 185°C marked by the dual valued flow activation energy and also by the temperature dependence of the tensile stress-strain curves. Increasing extrusion temperature increased both the flow activation energy and the extensional viscosity below the transition temperature.