A kinetic model for the enzyme-catalyzed self-epoxidation of oleic acid

This paper reports a kinetic model for the selfepoxidation of oleic acid with toluene as solvent and Novozym 435 (a commercially available preparation of immobilized Candida antarctica lipase) as catalyst at 30°C. The effects of various parameters on the conversion and rates of reaction were studied. Both the initial rate and the progress curve data were used to fit an ordered bi-bi model. At low temperatures, the rate of epoxidation was faster than the rate of deactivation of the enzyme by hydrogen peroxide.     

Mathematical modelling and its use for design of feeding strategies for L‐Sorbose fermentation

Batch sorbitol to sorbose bioconversion by Acetobacter suboxydans using initial sorbitol concentration (S₀ = 100 g/L) yielded a productivity of 10.11 g/L‐h and 98.6% conversion in 10 h time. The batch kinetics was then used to develop an unstructured mathematical model. Model parameters were identified using a nonlinear regression technique assisted by a computer program which minimized the deviation between the model predictions and actual batch experimental data. F test indicated 99% confidence on the prediction of model using optimized parameters. The batch model was eventually extrapolated to identify nutrient feeding strategies to maintain constant noninhibitory sorbitol supply and eliminate substrate limitation for fed‐batch fermentation in order to improve the sorbose productivity. The adequacy of the fed‐batch model was established by excellent agreement between experimental data and model simulation (except towards the end of fermentation).     

数据库技术在磷矿脱镁动力学中的应用

将现代计算机的数据库技术与反应动力学相结合，提出了使用数据库技术对膦矿脱镁动力学过程进行描述的新方法，并利用计算机对磷矿在二级串联釜中脱镁的过程进行了仿真模拟，其结果与实验值较为吻合。     

Synthesis and air separation of soluble terpolymers from Aniline,Toluidine, and Xylidine

A series of terpolymers were synthesized by oxidative polymerization of aniline, o-toluidine, and 2,3-xylidine with three monomer ratios using ammonium persulfate as an oxidant in two acidic media. The yield and intrinsic viscosity of the terpolymers were studied by changing the polymerization temperature and medium. The resulting terpolymers were characterized by ¹H–NMR, wide-angle X-ray diffraction, differential scanning calorimetry, thermogravimetry, and constant pressure-variable volume methods. The results showed that the terpolymers are amorphous and exhibit enhanced solubility, high thermostability, and high char yield, greater than 35 wt % at 900°C in nitrogen. A blend membrane of the terpolymer with ethyl cellulose shows good air-separation ability. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 790–798, 2001     

表面活性剂在非线性化学动力学研究中的应用

本文以化学振荡为例 ,系统地总结了表面活性剂在非线性化学动力学研究中的各种应用 ,包括对已知振荡反应的影响、引发的振荡反应 ,液膜振荡器及在等动力学关系探索中的应用等。     

Development of a green two‐dimensional HPLC‐DAD/ESI‐MS method for the determination of anthocyanins from Prunus cerasifera var. atropurpurea leaf and improvement of their stability in energy drinks

This study aimed to develop a green two‐dimensional HPLC‐DAD/ESI‐MS method for analysing anthocyanins from Prunus cerasifera var. atropurpurea leaf and improve their stability in energy drinks by the addition of phenolic acids. Ethanol and tartaric acid solutions were used as mobile phases for one‐dimensional HPLC‐DAD for quantitative analysis of anthocyanins, and the primary anthocyanins were identified as cyanidin‐3‐O‐galactoside, cyanidin‐3‐O‐glucoside and cyanidin‐3‐O‐rutinoside using two‐dimensional HPLC‐MS. Method validation showed that the developed method was accurate, stable and reliable for the analysis of P. cerasifera anthocyanins. The effects of gallic, ferulic and caffeic acid on the stability of cyanidin‐3‐O‐galactoside, cyanidin‐3‐O‐glucoside, cyanidin‐3‐O‐rutinoside and total anthocyanins from P. cerasifera leaf in energy drinks were evaluated, and the degradation of P. cerasifera anthocyanins ideally followed a first‐order model (R² > 0.98). Gallic acid showed stronger protective effects on P. cerasifera anthocyanins in energy drinks, and adding/increasing ferulic and caffeic acids accelerated the degradation reactions.     

New insight to the oxidation kinetics of silicon-containing steel at high temperature

This study investigated the oxidation kinetics of silicon-containing steel at 1150–1300 °C using a Simultaneous Thermal Analyzer under atmospheric conditions similar to that of an industry reheating furnace. There is a critical time point for the oxidation kinetics at an oxygen concentration of 4·0 vol.-%., following which the oxidation rate constant increases with the increasing oxidation temperature. The model coefficient A in the kinetic oxidation equation was found to be constant. However, before the critical time point, the oxidation rate constant remained unchanged; the model coefficient A decreased with the increasing temperature. Therefore, the kinetic model of silicon-containing steel for isothermal oxidation was observed to be a modified one on the basis of the experimental data. In addition, the critical time point was prolonged with the increasing isothermal oxidation temperature. Moreover, the oxidation activation energy of the tested silicon-containing steel was 366·16 kJ mol^?1.     

Hydrogels Based on 2-Hydroxyethylmethacrylate and Chitosan: Preparation,Swelling Behavior,and Drug Delivery

The authors report preparation of chitosan by deacetylation of chitin extracted from shrimp shells. The quality of chitosan depended on the chemical extraction process, the concentration of chemicals used, soaking time, sequence of deproteination, decalcification, and deacetylation. Hydrogels composed of hydroxyethylmethacrylate and chitosan were subsequently prepared and their swelling and ibuprofen delivery kinetics at various chitosan concentrations were studied. The swelling properties of the network varied with the chitosan concentration. Furthermore, the swelling process followed second-order kinetics, while ibuprofen diffusion into the hydrogel showed Fickian behavior.     

Peculiarities of the Thermal Degradation of Chlorosulphonated Polyethylenes

Abstract

A kinetic study is made of the thermal degradation of chlorosulphonated polyethylenes containing 3–40 wt% of Cl and 1.4–2.2 wt% of sulphur. It is concluded that the instability of these polymers is principally due to activation of the CHCl structures in the β-position to the [sbnd]CH₂[sbnd]SO₂Cl groups.     

Rheokinetic of a gelled resol resin curing by dynamic‐temperature rheometry based on rectangular torsion strain

The rheological behavior of a phenolic resol resin during its curing process was studied through a rheological dynamic‐temperature analysis. Two heating ramps from 0 to 120°C (1°C/min) and from 0 to 150°C (5°C/min) were performed. The resin's complex viscosity data were obtained by applying a rectangular torsion strain. The overall change of complex viscosity with temperature was due to a combination of thermal softening, described by the Andrade equation, and the resin crosslinking process. The four‐ and six‐parameter Arrhenius rheokinetic model was applied to the profiles obtained for the resin's complex viscosity, and the viscous flow and activation energies of curing kinetics were established. Two calculation methods are proposed to obtain the flow and curing parameters of the material. The six‐parameter Arrhenius model was more suitable for predicting changes in the resin's complex viscosity, obtaining an activation energy of ～ 38.0 kJ/mol for the resol resin curing process. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011