The mechanism of color reversion in soybean salad oil

An enzymatic reaction might be the major cause of color reversion in soybean oil. During the soybean flaking process, enzymatic reactions take place to convertγ-tocopherol to 5-(tocopheryloxy)-γ-tocopherol (γ-TED), and then further convertγ-TED to the precursors which are the cause of color reversion. The variations ofγ-tocopherol andγ-TED contents in soybean oil are accompanied by an inverse change in the precursors’ concentration. Therefore, the contents ofγ-tocopherol orγ-TED in crude soybean oil could be used as an index for predicting the color quality (color reversion) of soybean salad oil. Almost all the precursors (such as tocored) were converted to color-reverted substances under catalysis after bleaching treatment, and they were converted back to the precursors during deodorization. Those precursors might be gradually reconverted into the color reverted substances during storage to cause the color reversion in soybean salad oil.     

Hydrolytic degradation of polyglycolic acid: Tensile strength and crystallinity study

The hydrolytic degradation of polyglycolic acid (PGA) was studied by examining the changes of tensile strength and the level of crystallinity of the suture material. It was found that the breaking stress decreased from 6.369 × 10^?1 at 0 day to 3.97 × 10^?3 Newton/Tex at 49 days. The sigmodial shape of the stress–strain curves gradually disappeared with increase in the duration of in vitra degradation. The endpoint titration method used to assess the degree of degradation beyond the period of measurable tensile strength showed that the percent of PGA degraded were 42, 56, and 70% at 49, 60, and 90 days, respectively. The level of crystallinity of PGA at various durations of degradation exhibited an initial increase in the degree of crystallinity from 40% at 0 day to an upper limit of 52% at 21 days, then gradual decrease to 23% at 90 days. This observation is essentially parallel to hydrolysis of cellulose and polyethylene terephthalate. The concept of microfibrillar structure of fibers provides the basis for the proposed degradation mechanism of PGA in vitro. It is believed that degradation proceeds through two main stages which are different in rate of degradation.     

A rheological model for iron oxide suspensions

We have examined the rheological properties of a Co-adsorbed γ-Fe₂O₃ magnetic suspension with polyurethane (PU) as a binder and methyl ethyl ketone (MEK) or cyclohexanone (CH) as a solvent. A Haake RV20 viscometer was used to measure the suspension viscosity and the vane method was adopted to determine the fluid yield stress. A rheological model which can be viewed as a combination of the Casson model and the Bingham model is proposed to describe the suspension viscosity. The effects of temperature, particle content, and binder concentration are included in the model.     

高吸水性树脂的性能及应用

综述了高吸水性树脂的性能及其应用，并预测其广阔的开发前景。     

甲基丙烯酸缩水甘油酯的合成

在季铵盐催化作用下 ,甲基丙烯酸与环氧氯丙烷反应生成甲基丙烯酸缩水甘油酯。实验结果表明 ,二步法可获得较高的产率     

Packed bed electrodes. I. The electrochemical extraction of copper ions from dilute aqueous solutions

A study has been made of the cathodic deposition of copper ions from flowing dilute aqueous solutions onto a packed bed of graphite. The electrodeposition reaction is mass transfer controlled and expressions are presented for the cathodic current as a function of time, solution flow rate and bed characteristics. These have been verified from potentiostatic experiments. The cathode current efficiency is shown to approach 100% and packed bed electrodes are shown to be an effective means of extracting or removing metal ions from dilute solutions.     

An evaluation of commercial nickel catalysts during hydrogenation of soybean oil

The activities of several commercial nickel catalysts were determined by measuring their activation energies. Among these catalysts, G95E, Resan 22, Nysosel 222 and 325, all with low activation energy, were more active than DM3 and G95H, which had higher activation energy. However, the less active catalysts increased the linoleate selectivity of soybean oil during hydrogenation. The yields of bothtrans isomers and winterized oil were higher for the more selectively hydrogenated oil catalyzed by the less active catalysts. In the sensory evaluation, the fractionated solid fat that contained moretrans isomers was lower in flavor scores than the fractionated liquid oil after hydrogenation and winterization of soybean oil.     

An accelerated algorithm for full band electron–phonon scattering rate computation

Computing scattering rates of electrons and phonons stands at the core of studies of electron transport properties. In the high field regime, the interactions between all electron bands with all phonon bands need to be considered. This full band interaction implies a huge computational burden in calculating scattering rates. In this study, a new accelerated algorithm is presented for this task, which speeds up the computation by two orders of magnitude (100 times) and dramatically simplifies the coding. At the same time, it visually demonstrates the physical process of scattering more clearly.     

相位测量定位法在焦炉车辆上的应用与研究

文中通过测量载波相位进行定位的方法来解决焦炉车辆的定位问题，以达到无线定位的目的。并对定位的数学模型进行了详细的分析与论述。     

Recent studies of self-condensation and co-condensation of melamine-formaldehyde resins; cure at low temperatures

Self-condensation: recent research on the chemical pathways by which alcoholated melamine-formaldehyde (MF) resins react with themselves and on the product structures is summarized. Model compound studies suggest that bridges are less stable than widely thought unless they are in hexahydro-1,3,5-triazine ring structures. In acyclic structures they are probably less stable than bridges. Co-condensation: studies of how the composition of MF resins influences the rates of reaction with poly(ol) co-reactant show that MF resins that contain very low levels of and/or functionality are quite reactive. Reactivities of a variety of poly(ester) and acrylic coreactants were studied. By combining reactive MF resins with reactive co-reactants one can formulate high solids enamels that cure by co-condensation in 30 min at 50 to 65 °C with 0.5 parts per hundred (phr) of p-toluenesulfonic acid (p-TSA) catalyst. Cure at 25 °C appears feasible with higher catalyst levels.