Relationship between oxidative stability of vitamin E and production of fatty acids in oils during microwave heating

Effects of microwave heating on the oxidative stability ofd-tocopherols were studied in relation to the production of fatty acids in oils. During microwave heating, the stability of tocopherols decreased in the orderδ>β>γ>α. This order did not depend on the types of ethyl esters of fatty acids or oils present. But, the shorter the chainlength and the lower the degree of unsaturation of the fatty acid ethyl esters, the greater was the reduction in amount of individual tocopherols. A similar tendency was observed when tocopherol-stripped vegetable oils, with equimolar mixtures of tocopherols added, were treated under the same conditions. The reduction in tocopherols became greater with increasing levels of free fatty acids.     

Diffusion/adsorption model of cellulose dyeing. II. Ordinary cellulose–direct dye system

The diffusion and adsorption of C.I. Direct Yellow 12 and Blue 15 in water-swollen ordinary cellophane sheets were examined at various ionic strengths. The concentration dependence of apparent diffusion coefficients, D_c, for these dyes was obtained from the diffusion profiles in the substrate, which were measured by the use of the cylindrical film roll method. The decrease of apparent porosity with an increase in the amounts of adsorption was observed. To explain the diffusion/adsorption behaviors of these systems, a variable porosity model was proposed and was applied to analyze the concentration dependence of D_c's. The diffusion/adsorption behaviors of these dyes could be quantitatively described by this model at relatively low ionic strengths. At higher ionic strengths and/or lower values of C, i.e., at the large values of C_im/C_m, where the C's are the concentrations of immobilized (suffix im) and mobile (suffix m) species, it needed to introduce the concept of dynamic equilibria which occurred simultaneously with diffusion but deviated from the true equiliblia measured by the adsorption experiments.     

Depolymerization of fluoroalkyl methacrylate polymers as studied with thermogravimetry

Thermal behaviors of a few kinds of poly(fluoroalkyl methacrylate) prepared by γ-or UV-ray polymerization were investigated by using thermogravimetric measurements with the intermittent analysis of the gaseous products. The degradation of fluoroalkyl methacrylate polymers, monomeric units of which were CH₂=C(CH₃)COOCH₂(CF₂CF₂)_nH, n = 1, 2, and 3, proceeded according to the depolymerization mechanism reproducing the pristine monomer exclusively, but the thermogram in inert atmosphere showed the features of a two-step reaction. Two species of polymer differing in the heat stability were supposed to exist in the polymeric substance produced by γ- or UV-ray irradiation, and the fraction of polymer having lower heat stability increased with the increasing length of the fluoroalkyl ester group. In air, however, the thermogram of poly(fluoroalkyl methacrylate) showed no such a stepwise weight decrease as was observed in inert atomsphere with the elevating temperature, and the temperatures at which the depolymerization was introduced shifted to a much higher region. The results were ascribed to the reaction of initiating polymer radicals produced on polymer having lower stability with oxygen to form hydroperoxide, which once stabilized the polymer radicals and obstructed the initiaition of the unzipping reaction till higher temperature.     

Depolymerization of poly(fluoroalkyl methacrylate-co-methyl methacrylate) as studied with thermogravimetry

Thermal behaviors of a few kinds of poly(fluoroalkyl methacrylate-co-methyl methacrylate) prepared by γ-ray copolymerization were investigated by using thermogravimetric measurements together with the intermittent analysis of the gaseous products. The thermal degradation of copolymers composed of one of fluoroalkyl methacrylates of the following structures: CH₂?C(CH₃)COOCH₂(CF₂CF₂)_nH, where n = 1,2, and 3, and methyl methacrylate proceeded according to the depolymerization mechanism reproducing the pristine component comonomers exclusively, but their thermograms in inert atmosphere showed the feature of a two-step reaction. In air, however, thermograms of copolymers did not show such a stepwise decrease in weight with the elevating temperature, and temperatures at which depolymerization was introduced shifted to a much higher region. The overall aspects of depolymerization of copolymers seemed to be much similar to that of fluoroalkyl methacrylate homopolymer previously reported, and the retardation of depolymerization by air was considered to be due mainly to the stabilization of once-formed polymer radicals by oxygen.     

Selective Data Deactivation Mechanism in Sustainable Area-based Cache for Mobile Social Networks

This paper presents a proposal of a more resilient mechanism of an area-based sustainable cache system under a temporary decrease of the number of terminals. This mechanism suppresses interruptions of data relay and disappearances of cache data in the cache continually. The core technology enables each terminal to retain the received data in cache areas as ??deactivated data?? instead of deleting the data, even after a terminal leaves the area. Deactivated data are not relayed outside the target designated cache area. The data are reactivated and redistributed to others as relay data once the terminal revisits there. Consequently, the data are shared across time. Furthermore, particularly addressing the limitation of terminal storage, we proposed an adaptive scheme to select which data should be retained as deactivation data. This new mechanism leverages the proposed method under the storage limitation. As presented at the end of this paper, the simulation evaluations underscore the effectiveness of the proposed mechanism, and the adaptive selective scheme of deactivated data.     

Growth energetics of Lactococcus lactis subsp. lactis biovar diacetylactis in cometabolism of citrate and glucose

Certain strains of lactic acid bacteria present in commercial cheese starters, characterized by faint transparent colonies on an agar plate containing 1 mg kg ⁻¹ crystal violet (CVT), were identified as Lactococcus lactis subsp. (ssp) lactis biovar diacetylactis. The effect of citrate on the growth of these strains (CVT strains) in the presence of glucose was studied, in comparison with L. lactis strains. Molar growth yield from glucose (Y_G, g dry weight/mole of glucose consumed) for CVT strains grown on glucose plus citrate was significantly higher than the control (i.e. without citrate), but not for other L. lactis strains tested. Enhanced Y_G was also observed at a pH-controlled experiment, indicating that enhanced Y_G did not result from a buffering effect of citrate. CVT strains, in contrast to other strains of the same species, were shown to obtain enough energy to enhance Y_G on glucose–citrate mixtures.     

Improved efficiency of polymer light-emitting diodes by inserting a hole transport layer formed without thermal treatment above glass transition temperature

We have demonstrated a significant improvement in the performance of polymer light-emitting diodes (PLEDs) by inserting the fluorene-triatylamine copolymer as hole transport layer (HTL) without a thermal treatment above the glass transition temperature (T_g). A thin HTL insolubilized by a thermal treatment above T_g is often inserted as an interlayer between an anode buffer layer and a light-emitting polymer (LEP) in PLEDs fabricated by using a conventional solution process. The evaporative spray deposition using ultradiluted solution (ESDUS) method has enabled fabricating polymer bilayer structure without an insolublizing procedure. The bilayer PLEDs fabricated by ESDUS without the thermal treatment showed significantly higher and more stable external quantum efficiency than PLEDs having the conventional interlayer. Thermal treatment above T_g of the copolymer would induce degradation of its hole injection property. Furthermore, ESDUS bilayer devices showed much higher power efficiency than interlayer devices when calcium was used for cathode. The improvements would be caused by the enhancement of hole injection and the effective electron blocking at the copolymer/LEP interface in the ESDUS bilayer devices.     

掺锡As2S8非饱和光阻断效应实验与机理研究

为了研究微量Sn掺As2S8非晶态薄膜波导非饱和光阻断效应的内在机理,采用双棱镜耦合技术,对波导样品进行了实验研究,在实验观测数据,分析了薄膜材料内部的化学键结构,结合电子能带理论和轨道杂化理论,建立了非饱和光阻断效应的动力学模型,并对实验数据进行数值拟合,得到了描述非饱和光阻断效应性质的参数。数值分析与实验结果吻合,说明本文模型能解释实验现象,揭示实验本质。