Color control of Japanese soy sauce (shoyu) using membrane technology

The present study systemically decolorized soy sauce using a membrane process to analyze the separation mechanism. An ultrafiltration (UF) membrane (NTU-2120) exhibited only slight decolorization ability. A nanofiltration (NF) membrane with a lower molecular weight cut-off and produced by sulfonated polysulfone (NTR-7400 series) rather than polyvinyl alcohol/polyamide (NTR-7250) had higher decolorization ability. The NF membranes rejected total nitrogen by 17–24%, unsalted soluble solid content by 24–32%, reducing sugar by 25–43%, and amino acids by 10–25%. The NTR-7400 series membrane rejected lactic acid by 6–9%, and pyroglutamic acid by 11–21%; other quality indexes were maintained. In the NF membrane processes, higher rejection of acidic amino acids than neutral and base amino acids was observed. The separation performance was governed by the electrical effect as well as the sieve effect. Soy sauce color could be controlled by blending NF membrane-processed soy sauce with feed soy sauce. Color can be matched to preference in accordance with dishes by suitably blending NF membrane-processed soy sauce with feed soy sauce.     

Optical Active Nano-Glass-Ceramics

This paper reviews the synthesis and characterization of several transparent glass-ceramics with optical active nanocrystals. Glass-ceramics containing ferroelectric Sr_xBa_1-xNb₂O₆ nanocrystals with an ellipsoidal shape show optical phase modulations in the presence of alternative electric fields. In the glass-ceramics with Ba₂TiSi₂O₈ (BTS) nanocrystals, BTS crystalline layers with a thickness of approximately 120 nm are formed at the surface and ellipsoidal-shaped crystallites with a diameter of 100–200 nm are dispersed in the glass matrix. Some TeO₂-based and GeO₂-based glasses show a prominent nanocrystallization. RE-doped CaF₂ nanocrystals are patterned in a spatially selected region by laser irradiations. The size, morphology, and dispersion state of nanocrystals should be carefully checked in each glass system and composition. The basic concept for the design of glass system and composition is also discussed. Some data on optical active performances in transparent glass-ceramics with nanocrystals were introduced.     

Crystalline Phases and YAG Laser-Induced Crystallization in Sm2O3–Bi2O3–B2O3 Glasses

The glass formation region, crystalline phases, second harmonic (SH) generation, and Nd:yttrium aluminum garnet (YAG) laser-induced crystallization in the Sm₂O₃–Bi₂O₃–B₂O₃ system were clarified. The crystalline phases of Bi₄B₂O₉, Bi₃B₅O₁₂, BiBO₃, Sm _x Bi_{1− x} BO₃, and SmB₃O₆ were formed through the usual crystallization in an electric furnace. The crystallized glasses consisting of BiBO₃ and Sm _x Bi_{1− x} BO₃ showed SH generations. The formation of the nonlinear optical BiB₃O₆ phase was not confirmed. The formation (writing) region of crystal lines consisting of Sm _x Bi_{1− x} BO₃ by YAG laser irradiation was determined, in which Sm₂O₃ contents were∼10 mol%. The present study demonstrates that Sm₂O₃–Bi₂O₃–B₂O₃ glasses are promising materials for optical functional applications.     

Photoluminescence of Rare-Earth-Doped Ca-α-SiAlON Phosphors: Composition and Concentration Dependence

Rare-earth-doped Ca-α-SiAlON phosphors, with the compositions of (Ca_{1−3/2 x} RE _x ) _{m /2}Si_{12− m − n} Al _m+n O _n N_{16− n} (RE=Ce, Sm, and Dy, 0.5≤ m =2 n ≤3.0), were prepared by sintering at 1700°C for 2 h under 10 atm N₂. The concentration of rare earths varied from 3 to 30 at.% with respect to Ca. The photoluminescence (PL) properties were investigated as functions of the composition of the host matrix (i.e., m ) and the concentration of rare earths (i.e., x ). The results show that the emission properties can be optimized by tailoring m and x . The Ce³⁺ luminescence originating from the 4 f –5 d interconfigurational transitions is greatly affected by the environment surrounding the Ce³⁺ ions, which differs from the Sm³⁺ or Dy³⁺ luminescence arising from the 4 f –4 f intraconfigurational transitions. X-ray diffraction and scanning electron microscopy were used to explain the composition and concentration dependence of PL properties.     

Preparation and characterization of electroplated amorphous gold-nickel alloy film for electrical contact applications

A process for electroplating amorphous gold-nickel alloy with the atomic ratio of unity was developed. The plating bath was prepared by adding potassium cyanoaurate(I) into a known plating bath which produces amorphous nickel-tungsten alloy. At a sufficiently high gold concentration, the alloy deposit did not contain any tungsten. The amorphous nature of the Au-Ni alloy produced in the new bath was confirmed by using TEM and THEED. Hardness, resistivity, and contact resistance of this new alloy were determined, and the results are discussed for applications as an electrical contact material.     

The Wulff Shape of Alumina: II, Experimental Measurements of Pore Shape Evolution Rates

The rate at which a facetted tetragonal cavity of nonequilibrium shape approaches a cubic equilibrium (Wulff) shape via surface diffusion was modeled. The shape relaxation rate of a facetted stretched cylinder was also modeled. For the first geometry, only an approximate solution based on linearizing the mean potential difference between the source and sink facets was obtained. For the stretched cylinder, both an approximate and an exact solution can be obtained; the approximate solution underestimates the evolution rate by a factor of ∼2. To assess the applicability of the models, nonequilibrium shape pores of identical initial geometry (∼20 μm × 20 μm × 0.5 μm) were introduced into (0001), {10[Onemacr]2}, {1120}, and {100} surfaces of sapphire single crystals using microfabrication techniques, ion-beam etching, and hot pressing. The large (∼20 μm × 20 μm) faces of the pore are low-index surfaces whose nature is dictated by the wafer orientation. A series of anneals was performed at 1900°C, and the approach of the pore shape to an equilibrium shape was monitored. The kinetics of shape evolution are highly sensitive to the crystallographic orientation and stability of the low-index surface that dominates the initial pore shape. The measured variations of the pore aspect ratio were compared to those predicted by the kinetic model. The observations suggest that when the initial bounding surface is unstable, shape relaxation may be controlled by diffusion. However, surface-attachment-limited kinetics (SALK) appears to play a major role in determining the pore shape evolution rate in cases where the initial bounding surfaces have orientations that are part of the Wulff shape.     

Kinetics of Enthalpy Relaxation at the Glass Transition in Ternary Tellurite Glasses

The kinetics of enthalpy relaxation (recovery) at the glass transition in x K₂O·(20− x )MgO·80TeO₂ glasses has been examined from heat capacity measurements using differential scanning calorimetry to clarify the features of the structural relaxation in ternary TeO₂-based glasses. Ternary glasses such as 10K₂O·10MgO·80TeO₂ show high thermal resistance against crystallization compared with binary glasses. The degree of fragility m estimated from the activation energy for viscous flow E _η and the glass transition temperature T _g is m = 55–62, indicating a fragile character in TeO₂-based glasses. Large heat capacity changes of 43.1–48.2 J·mol⁻¹·K⁻¹ are also observed at the glass transition. The activation energy for enthalpy relaxation Δ H is evaluated from the cooling rate dependence of the limiting fictive temperature, and values of Δ H = 897–1268 kJ·mol⁻¹ are obtained. Negative deviation from additivity in Δ H is also observed. Values of the Kovacs–Aklonis–Huchinson–Ramos (KAHR) parameter θ estimated from Δ H and T _g are 0.33–0.42 K⁻¹. It has been proposed that ternary glasses have more homogeneous and constrained glass structure compared with binary glasses.     

Effect of crosslinking structure on sorption of CO2 in photocrosslinked PVCA film

The sorption behavior of CO₂ gas in photocrosslinked poly(vinyl cinnamate) film was examined under atmospheric pressure. The sorption isotherm was well described by the Langmuir equation, suggesting that sorption of CO₂ is mainly governed by adsorption in the microvoids. The amount of sorbed CO₂ was significantly affected by the degree of crosslinking. The CO₂ sorption was enhanced at a lower degree of crosslinking but was decreased at a higher degree of crosslinking. The unexpected increase in the amount of adsorbed CO₂ correlated with the increase in the number of microvoids that occurred as a result of the crosslinking reaction. However, further crosslinking led to a decrease in the mean size of the microvoids. The smaller microvoids, in comparison to CO₂ molecules, did not act as adsorption sites, so that the amount of sorbed CO₂ decreased. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 1744–1750, 2000     

Cathodic performance of LiMn1−xMxPO4 (M = Ti, Mg and Zr) annealed in an inert atmosphere

To improve the cathodic performance of olivine-type LiMnPO₄, we investigated the optimal annealing conditions for a composite of carbon with cation doping. Nanocrystalline and the cation-doped LiMn_1−xM_xPO₄ (M = Ti, Mg, Zr and x = 0, 0.01, 0.05 and 0.10) was synthesized in aqueous solution using a planetary ball mill. The synthesis was performed at the fairly low temperature of 350 °C to limit particle size. The obtained samples except for the Zr doped one consisted of uniform and nano-sized particles. The performance of LiMnPO₄ was much improved by an annealing treatment between 500 and 550 °C with carbon in an inert atmosphere. A small amount of metal-rich phosphide (Mn₂P) was detected in the sample annealed at 900 °C. In addition, 1 at.% Mg doping for Fe enhanced the rate capability in our doped samples. The discharge capacity of LiMn_0.99Mg_0.01PO₄/C was 146 mAh/g at 0.1 mA/cm² and 125 mAh/g even at 2.0 mA/cm².     

Temperature- and pH-responsive photosensitization activity of polymeric sensitizers based on poly-N-isopropylacrylamide

We previously reported that a copolymer consisting of N-isopropylacrylamide (NIPAM) and benzophenone (BP) units, behaves as a photosensitizer showing temperature-controlled oxygenation activity in water (J. Am. Chem. Soc.2006, 128, 8751). This polymer shows a heat-induced oxygenation enhancement at low temperature region (5-20 °C), while showing a heat-induced oxygenation suppression at high temperature region (20-60 °C), resulting in an off-on-off activity profile against the temperature window. This is driven by a heat-induced phase transition of the polymer from coil to micelle and then to globule states. In the present work, effects of adding an amine component (N-[3-(dimethylamino)propyl]acrylamide: DMAPAM) to the polymer on the sensitization activity were studied, where the relationship between the phase transition behavior and the activity was clarified by several spectroscopic analyses. The polymers, poly(NIPAM_x-co-BP_y-co-DMAPAM_z), show activity controlled by temperature and pH. The off-on-off activity profile shifts to higher temperature with a pH decrease. This is because protonation of the DMAPAM units leads to an increase in the polymer polarity and, hence, the polymer aggregates at higher temperature. In addition, increase in the DMAPAM content of the polymer leads to further shift of the activity profile. In contrast, at pH < 8, no activity enhancement is observed because complete protonation of the DMAPAM units suppresses polymer aggregation.