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1.
Epoxy novolac/anhydride cure kinetics has been studied by differential scanning calorimetry under isothermal conditions. The system used in this study was an epoxy novolac resin (DEN431), with nadic methyl anhydride as hardener and benzyldimethylamine as accelerator. Kinetic parameters including the reaction order, activation energy and kinetic rate constants, were investigated. The cure reaction was described with the catalyst concentration, and a normalized kinetic model developed for it. It is shown that the cure reaction is dependent on the cure temperature and catalyst concentration, and that it proceeds through an autocatalytic kinetic mechanism. The curing kinetic constants and the cure activation energies were obtained using the Arrhenius kinetic model. A suggested kinetic model with a diffusion term was successfully used to describe and predict the cure kinetics of epoxy novolac resin compositions as a function of the catalyst content and temperature. Copyright © 2003 Society of Chemical Industry 相似文献
2.
加氢渣油催化裂化七集总动力学模型的建立 总被引:1,自引:0,他引:1
以加工加氢渣油的茂名石化3^#重油催化裂化装置的工业数据为基础,针对加氢渣油的特点,提出了以渣油四组分作为划分原料集总基础的催化裂化七集总动力学模型。通过变尺度法(B-F-G-S)和龙格库塔法确定动力学参数,并通过工业实测数据验证,表明该模型具有良好的拟合性和外推性,较好地反映了加氢渣油催化裂化反应规律。 相似文献
3.
4.
枪械振动测试包含刚体线位移和角位移六维运动参数.其测试方法是,将光电传感器光源与被测体固结在一起,通过求解光源在三个投影屏上随着被测体运动变化的数学模型而实现的.该传感器由激光器、投影屏、光电探测器件及处理电路、数据采集、数据处理等部分组成.并以固结在被测体上的三个激光器的交点为基点,建立其线位移数学模型;以方向余弦法来确定被测体的角位移,建立其角位移数学模型. 相似文献
5.
6.
Omar Snchez Estrella Asp María C Martí Marlene Roeckel 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2005,80(11):1261-1267
Most of the kinetic studies on nitrification have been performed in diluted salts medium. In this work, the ammonia oxidation rate (AOR) was determined by respirometry at different ammonia (0.01 and 33.5 mg N‐NH3 L?1), nitrite (0–450 mg N‐NO2? L?1) and nitrate (0 and 275 mg N‐NO3? L?1) concentrations in a saline medium at 30 °C and pH 7.5. Sodium azide was used to uncouple the ammonia and nitrite oxidation, so as to measure independently the AOR. It was determined that ammonia causes substrate inhibition and that nitrite and nitrate exhibit product inhibition upon the AOR. The effects of ammonia, nitrite and nitrate were represented by the Andrews equation (maximal ammonia oxidation rate, rAOMAX, = 43.2 [mg N‐NH3 (g VSSAO h)?1]; half saturation constant, KSAO, = 0.11 mg N‐NH3 L?1; inhibition constant KIAO, = 7.65 mg N‐NH3 L?1), by the non‐competitive inhibition model (inhibition constant, KINI, = 176 mg N‐NO2? L?1) and by the partially competitive inhibition model (inhibition constant, KINA, = 3.3 mg N‐NO3? L?1; α factor = 0.24), respectively. The rAOMAX value is smaller, and the KSAO value larger, than the values reported in diluted salts medium; the KIAO value is comparable to those reported. Process simulations with the kinetic model in batch nitrifying reactors showed that the inhibitory effects of nitrite and nitrate are significant for initial ammonia concentrations larger than 100 mg N‐NH4+ L?1. Copyright © 2005 Society of Chemical Industry 相似文献
7.
In this work a new class of numerical methods for the BGK model of kinetic equations is presented. In principle, schemes of
any order of accuracy in both space and time can be constructed with this technique. The methods proposed are based on an
explicit–implicit time discretization. In particular the convective terms are treated explicitly, while the source terms are
implicit. In this fashion even problems with infinite stiffness can be integrated with relatively large time steps. The conservation
properties of the schemes are investigated. Numerical results are shown for schemes of order 1, 2 and 5 in space, and up to
third-order accurate in time. 相似文献
8.
Chia‐Yin Chen Yu‐Chi Cheng Shau‐Wei Tsai 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2002,77(6):699-705
A lipase‐catalyzed enantioselective hydrolysis process under in situ racemization of the remaining (R)‐thioetser substrate with trioctylamine as the catalyst was developed for the production of (S)‐fenoprofen from (R,S)‐fenoprofen 2,2,2‐trifluoroethyl thioester in isooctane. Detailed investigations of trioctylamine concentration on the enzyme activation and the kinetic behavior of the thioester in racemization and enzymatic reactions were conducted, in which good agreement between the experimental data and theoretical results was observed. © 2002 Society of Chemical Industry 相似文献
9.
V. A. Roginsky T. K. Barsukova A. A. Remorova W. Bors 《Journal of the American Oil Chemists' Society》1996,73(6):777-786
The relative reactivities as well as the stoichiometric coefficients for a number of flavonoids, catechols, and—for comparison—standard
phenolic antioxidants were determined by analyzing the kinetics of oxygen consumption in organic and micellar systems, with
peroxidation initiated by lipid- and water-soluble azo initiators. The results demonstrated that the flavonoids did not behave
as classic phenolic antioxidants such as α-tocopherol, but showed only moderate chain-breaking activities. The results were
in line with other structure-activity relationship studies on the importance of the B-ring catechol structure, the 2,3-double
bond, and the 3,5-hydroxy groups. The data are discussed in view of possible explanations of the deviations flavonoids reveal
in their behavior compared with regular phenolic antioxidants. 相似文献
10.
N. JostJ. Karger-Kocsis 《Polymer》2002,43(4):1383-1389
Curing kinetics of a vinylester-urethane hybrid (VEUH) resin consisting of vinylester resin (VE) diluted in styrene and novolac type polyisocyanate (NPI) have been studied by differential scanning calorimetry (DSC). As VEUH is crosslinked via free radical polymerisation between the vinyl functions of styrene and VE, and polyaddition reaction between the secondary -OH groups of VE and -NCO of NPI, it was necessary to study these reactions separately. This was achieved by studying the curing with and without incorporating the NPI. The curing reaction was monitored by measuring the heat of reaction under isothermal and dynamic temperature conditions. Models describing the curing were developed, which are in good agreement with the experiments. A comparison between the curing of the VEUH and the VE resin without NPI leads to the conclusion that the curing of the VEUH as accessed by DSC is dominated by the radical polymerisation of styrene with VE although the two reactions are not time separated. 相似文献