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首页> 外文期刊>Journal of Applied Polymer Science >Methacrylate/acrylate terminated derivatives of diglycidyl hexahydrophthalate: Synthesis, structural, and thermal characterization
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Methacrylate/acrylate terminated derivatives of diglycidyl hexahydrophthalate: Synthesis, structural, and thermal characterization

机译:六氢邻苯二甲酸二缩水甘油酯的甲基丙烯酸酯/丙烯酸酯封端的衍生物:合成,结构和热表征

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Mono- or di(meth)acrylate-terminated derivatives of diglycidyl hexahydrophthalate (ER) were prepared by reacting 1:1 or 1:2M ratio of ER and methacrylic acid or acrylic acid. These vinyl ester (VE) resins were characterized by determining epoxy equivalent weight, acid number, and molecular weight by gel permeation chromatography. Structural characterization was done by FTIR and H-1 NMR spectroscopy. In the H-1 NMR spectra of acrylate-terminated VE resins, three proton resonance signals were observed in the region 5.8-6.4 ppm due to vinyl group while in methacrylate-terminated VE resins only two proton resonance signals due to vinylidene protons were observed at 5.6-6.1 ppm. The Brookfield viscosity (room temperature (25 +/- 2)degrees C) of these resins diluted with varying amounts of MMA was determined at 20 rpm. Curing behavior was monitored by determination of gel time and differential scanning calorimetry. An exothermic transition was observed in the DSC scans in the temperature range of (81-150)degrees C. Isothermal curing of MMA-diluted VE resins containing AIBN as an initiator was done at 60 degrees C for 2 h in N-2 atmosphere, and then heating for another 2 h in static air atmosphere. Thermal stability of isothermally cured resins in N-2 atmosphere was evaluated by thermogravimetric analysis. All cured resins decomposed above 310 degrees C in single step. Thermal stability of the cured resins having acrylate end caps was marginally higher than the resins having methacrylate end groups. (c) 2005 Wiley Periodicals, Inc.
机译:通过使比例为1:1或1:2M的ER与甲基丙烯酸或丙烯酸反应,制得六氢邻苯二甲酸二缩水甘油酯的单或二(甲基)丙烯酸酯封端的衍生物。这些乙烯基酯(VE)树脂的特征在于通过凝胶渗透色谱法测定环氧当量,酸值和分子量。通过FTIR和H-1 NMR光谱进行结构表征。在丙烯酸​​酯封端的VE树脂的H-1 NMR光谱中,在5.8-6.4 ppm范围内由于乙烯基而观察到三个质子共振信号,而在甲基丙烯酸酯封端的VE树脂中仅在亚乙烯基质子引起的两个质子共振信号被观察到5.6-6.1 ppm。在20rpm下测定用不同量的MMA稀释的这些树脂的布鲁克菲尔德粘度(室温(25 +/- 2)℃)。通过确定胶凝时间和差示扫描量热法监测固化行为。在(81-150)℃的温度范围内的DSC扫描中观察到放热转变。含有AIBN作为引发剂的MMA稀释VE树脂的等温固化在N-2气氛中于60℃进行2 h,然后在静态空气中再加热2小时。通过热重分析评价在N-2气氛中等温固化的树脂的热稳定性。所有固化树脂在310摄氏度以上均会一步分解。具有丙烯酸酯端基的固化树脂的热稳定性略高于具有甲基丙烯酸酯端基的树脂。 (c)2005年Wiley Periodicals,Inc.

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