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Structure property relationships of biobased n-alkyl bisferulate epoxy resins

机译:生物基正烷基双阿魏酸酯环氧树脂的结构性质关系

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In this work, a series of bio-based chemically recyclable epoxy resins were synthesized from n-alkyl bis-ferulate esters that do not activate human estrogen receptor alpha (ERa). Viscosities of corresponding glycidyl ether n-alkyl bisferulate resins, determined by steady shear rheology, range from 12-9.4 Pa s. Activation energies of flow range from 83-96 kJ mol(-1) and are similar to the diglycidyl ether bisphenol A (DGEBA). Thermomechanical properties of diglycidyl ether n-alkyl bisferulate resins cured with isophorone diamine were governed by the length of alpha,omega-diols that link glycidyl ether ferulate units. That is, the glassy phase modulus and alpha transition temperatures range from 3400-2400 MPa (at 25 degrees C) and 40-53 degrees C (peak of E''), respectively. Furthermore, the onset of thermal degradation (T-d5%) varied from 331-300 degrees C. Chemical recycling of cured epoxy resins was performed by static immersion in 10 w/w sodium hydroxide aqueous solutions at 60 degrees C. Times required for complete conversion of cured resins to water-soluble degradation products was also alpha,omega-diol length dependent and varied from 5 to 65 h. Thus, diglycidyl ether of n-alkyl bisferulate resins provides a viable biobased alternative to BPA epoxy resins as well as the option of chemical degradability and recovery of fillers in composite applications.
机译:在这项工作中,从不激活人类雌激素受体α(ERa)的正烷基双阿魏酸酯合成了一系列生物基化学可循环利用的环氧树脂。通过稳定的剪切流变学确定的相应缩水甘油醚正烷基二阿魏酸酯树脂的粘度为12-9.4Pa·s。流动的活化能范围为83-96 kJ mol(-1),类似于二缩水甘油醚双酚A(DGEBA)。用异佛尔酮二胺固化的二缩水甘油基醚正烷基二阿魏酸酯树脂的热机械性能受连接缩水甘油基醚阿魏酸酯单元的α,ω-二醇的长度支配。即,玻璃相模量和α转变温度分别在3400-2400MPa(在25℃)和40-53℃(E”的峰值)的范围内。此外,热降解的开始时间(T-d5%)在331-300摄氏度之间变化。固化的环氧树脂的化学循环通过在60摄氏度的温度下静态浸入10 w / w的氢氧化钠水溶液中进行。固化树脂向水溶性降解产物的转化率也取决于α,ω-二醇的长度,从5小时到65小时不等。因此,正烷基二阿魏酸酯树脂的二缩水甘油醚为BPA环氧树脂提供了一种可行的生物基替代品,并且在复合应用中提供了化学降解性和填料回收的选择。

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