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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
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本文阐述了通过Friedel-Crafts反应合成邻-(4-乙基苯甲酰基)苯甲酸的方法.研究了影响产物质量的因素,提出了适宜的工艺条件. 相似文献
3.
马来酸酐在乙丙橡胶上的接枝共聚 总被引:4,自引:0,他引:4
马来酸酐在乙丙橡胶上的接枝共聚,用过氧化苯甲酰为引发剂的效果优于偶氮二异丁腈。研究了温度、马来酸酐用量和引发剂用量等对接枝率的影响。用红外光谱和薄层色谱证明了接枝物的存在。用接触角技术测定了接枝物的表面性能。 相似文献
4.
Toru Ikegami Hideyuki Negishi Dai Kitamoto Keiji Sakaki Tomohiro Imura Masayoshi Okamoto Yasushi Idemoto Nobuyuki Koura Tsuneji Sano Kenji Haraya Hiroshi Yanagishita 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2005,80(4):381-387
In order to produce highly concentrated bioethanol by pervaporation using an ethanol‐permselective silicalite membrane, techniques to suppress adsorption of succinic acid, which is a chief by‐product of ethanol fermentation and causes the deterioration in pervaporation performance, onto the silicalite crystals was investigated. The amount adsorbed increased as the pH of the aqueous succinic acid solution decreased. The pervaporation performance also decreased with decreasing pH when the ternary mixtures of ethanol/water/succinic acid were separated. Using silicalite membranes individually coated with two types of silicone rubber, pervaporation performance was significantly improved in the pH range of 5 to 7, when compared with that of non‐coated silicalite membranes in ternary mixtures of ethanol/water/succinic acid. Moreover, when using a silicalite membrane double‐coated with the two types of silicone rubber, pervaporation performance was stabilized at lower pH values. In the separation of bioethanol by pervaporation using the double‐coated silicalite membrane, removal of accumulated substances having an ultraviolet absorption maximum at approximately 260 nm from the fermentation broth proved to be vital for efficient pervaporation. Copyright © 2005 Society of Chemical Industry 相似文献
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马来酸及其酐和衣康酸与PP熔体接枝反应机理的研究 总被引:13,自引:0,他引:13
以马来酸酐作对照,用热分析、流变、化学分析等方法,研究了马来酸和衣康酸在非隔氧条件下与PP熔体催化接枝反应的特点和规律,阐述了单体结构-单元反应相对速率--接枝产物结构之间的关系,提出了3种接枝物的结构模型。 相似文献
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以偏苯三甲酸酐和氯化亚砜为原料 ,其摩尔比为 1:1 2 ,在回流状态下首先合成中间体 4 -氯甲酰基苯甲酸酐Ⅱ ,产率可达 98%。Ⅱ经过胺化、减压脱水制得 4 -氰基苯甲酸酐 ,其沸点为 175~ 180 C/ 0 2 6KPa ,各反应物摩尔比为n (Ⅱ ) :n (NH3 ) :n (P2 O5) =1 0 :4 7:2 1。通过红外分析、1H -NMR分析及元素分析证明 ,所得到的化合物即为目标物。 相似文献
9.
A series of polyurethane microcapsules containing a phase change material (PCM) of n‐octadecane was successfully synthesized by an interfacial polymerization in aqueous styrene‐maleic anhydride (SMA) dispersion with diethylene triamine (DETA) as a chain extender reacting with toluene‐2,4‐diisocyanate (TDI). The average diameter of microPCMs is in the range of 5–10 μm under the stirring speed of 3000–4000 rpm. Optical and SEM morphologies of microPCMs had ensured that the shell was regularly fabricated with the influence of SMA. FTIR results confirmed that the shell material was polyurethane and the SMA chains associated on core material reacted with TDI forming a part of shell material. The shell thickness was decreasing in the range of 0.31–0.55 μm with the molar ratio of DETA/TDI from 0.84 to 1.35 and the weight of core material increasing from 40 to 80% (wt %). By controlling the weight ratio of PCM as 40, 50, 60, 70, and 80% in microPCMs, it was found using DSC that the Tm and Tc of microPCMs were in the range of 29.8–31.0oC and 21.1–22.0°C and an obvious phase change had been achieved nearly the same temperature range of that of PCM. The results from release curves of microPCM samples prepared by 1.4, 1.7, and 2.0 g of SMA indicated the release properties were affected by the amount of the dispersant, which attributed to the emulsion effect and shell polymerization structure. The above results suggest that the shell structure of microPCMs can be controlled and the properties of microPCMs determined by shell will perform proper practical usage. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4996–5006, 2006 相似文献
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