首页> 美国卫生研究院文献>Materials >Synthesis and Thermal Properties of Acrylonitrile/Butyl Acrylate/Fumaronitrile and Acrylonitrile/Ethyl Hexyl Acrylate/Fumaronitrile Terpolymers as a Potential Precursor for Carbon Fiber
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Synthesis and Thermal Properties of Acrylonitrile/Butyl Acrylate/Fumaronitrile and Acrylonitrile/Ethyl Hexyl Acrylate/Fumaronitrile Terpolymers as a Potential Precursor for Carbon Fiber

机译:丙烯腈/丙烯酸丁酯/富马腈和丙烯腈/乙基己酸乙酯/富马腈三元共聚物作为碳纤维的潜在前体的合成和热性能

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摘要

A synthesis of acrylonitrile (AN)/butyl acrylate (BA)/fumaronitrile (FN) and AN/EHA (ethyl hexyl acrylate)/FN terpolymers was carried out by redox polymerization using sodium bisulfite (SBS) and potassium persulphate (KPS) as initiator at 40 °C. The effect of comonomers, BA and EHA and termonomer, FN on the glass transition temperature (Tg) and stabilization temperature was studied using Differential Scanning Calorimetry (DSC). The degradation behavior and char yield were obtained by Thermogravimetric Analysis. The conversions of AN, comonomers (BA and EHA) and FN were 55%–71%, 85%–91% and 76%–79%, respectively. It was found that with the same comonomer feed (10%), the Tg of AN/EHA copolymer was lower at 63 °C compared to AN/BA copolymer (70 °C). AN/EHA/FN terpolymer also exhibited a lower Tg at 63 °C when compared to that of the AN/BA/FN terpolymer (67 °C). By incorporating BA and EHA into a PAN system, the char yield was reduced to ~38.0% compared to that of AN (~47.7%). It was found that FN reduced the initial cyclization temperature of AN/BA/FN and AN/EHA/FN terpolymers to 228 and 221 °C, respectively, in comparison to that of AN/BA and AN/EHA copolymers (~260 °C). In addition, FN reduced the heat liberation per unit time during the stabilization process that consequently reduced the emission of volatile group during this process. As a result, the char yields of AN/BA/FN and AN/EHA/FN terpolymers are higher at ~45.1% and ~43.9%, respectively, as compared to those of AN/BA copolymer (37.1%) and AN/EHA copolymer (38.0%).
机译:以亚硫酸氢钠(SBS)和过硫酸钾(KPS)为引发剂,通过氧化还原聚合合成丙烯腈(AN)/丙烯酸丁酯(BA)/富马腈(FN)和AN / EHA(丙烯酸乙基己酯)/ FN三元共聚物。在40°C下。使用差示扫描量热法(DSC)研究了共聚单体BA和EHA以及三聚单体FN对玻璃化转变温度(Tg)和稳定温度的影响。通过热重分析获得降解行为和炭产率。 AN,共聚单体(BA和EHA)和FN的转化率分别为55%–71%,85%–91%和76%–79%。发现在相同的共聚单体进料(10%)下,与AN / BA共聚物(70℃)相比,AN / EHA共聚物的Tg在63℃下较低。与AN / BA / FN三元共聚物(67°C)相比,AN / EHA / FN三元共聚物在63°C下的Tg也较低。通过将BA和EHA合并到PAN系统中,与AN(约47.7%)相比,焦炭产率降低至〜38.0%。结果发现,与AN / BA和AN / EHA共聚物相比,FN将AN / BA / FN和AN / EHA / FN三元共聚物的初始环化温度分别降低至228和221°C(〜260°C )。另外,FN减少了稳定过程中每单位时间的热量释放,从而减少了该过程中挥发性基团的释放。结果,与AN / BA共聚物(37.1%)和AN / EHA相比,AN / BA / FN和AN / EHA / FN三元共聚物的炭收率分别更高,分别为〜45.1%和〜43.9%。共聚物(38.0%)。

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