Polymer Science and Technology, Istanbul Technical University, Maslak, 34469 Istanbul, Turkey.
Department of Textile Engineering, Istanbul Technical University, Gumussuyu, 34437 Istanbul, Turkey.
J Nanosci Nanotechnol. 2019 Jul 1;19(7):3844-3853. doi: 10.1166/jnn.2019.16309.
This study aimed to produce poly(acrylonitrile-co-vinylacetate-co-itaconic acid) (poly(AN-co-VAc-co-IA)) terpolymer as a carbon nanofiber precursor. In this respect, terpolymer samples with different IA amounts were synthesized by free radical polymerization. Produced terpolymer samples were electrospun in order to obtain nanofibers which were then converted to carbon nanofibers. Obtained electrospun nanofibers were oxidized at different temperatures between 200-325 °C. After the oxidation process, carbonization process was applied at 1100 °C in the presence of N₂. Viscosity and molecular weight distribution of produced samples were measured with ubbelohde viscosimeter and gel permeation chromatography (GPC), respectively. Thermal features of the ter-polymer samples were analyzed by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). Spectroscopic characterization of terpolymer samples, oxidized and carbonized nanofibers were performed by Fourier transform infrared-attenuated total reflectance (FTIR-ATR). Original electrospun nanofibers, oxidized and carbonized nanofibers were investigated morphologically by scanning electron microscope (SEM). Inclusion of IA had considerable effect on terpolymer properties and electrospun nanofibers. Moreover, it was proven that oxidation temperature was a crucial parameter for carbon nanofiber production from terpolymer. Both morphology and color of the produced nanofiber mats changed when carbonization process was accomplished. It was observed that poly(AN-co-VAc-co-IA) terpolymer has lower initiation temperature when compared to poly(AN-co-VAc) and poly(AN-co-IA) copolymers, giving the opportunity to obtain carbon nanofibers easier, and poly(AN-co-VAc-co-IA) terpolymer can be used as an effective precursor for carbon nanofiber production.
本研究旨在制备聚(丙烯腈-共-醋酸乙烯酯-共-衣康酸)(poly(AN-co-VAc-co-IA))三元共聚物作为碳纤维前驱体。为此,通过自由基聚合合成了不同 IA 含量的三元共聚物样品。为了得到纳米纤维,将制备的共聚物样品进行静电纺丝,然后将纳米纤维转化为碳纤维。所得静电纺纳米纤维在 200-325°C 之间的不同温度下进行氧化。氧化后,在 N₂存在下于 1100°C 进行碳化。使用乌贝洛德粘度计和凝胶渗透色谱(GPC)分别测量所制备样品的粘度和分子量分布。通过热重分析(TGA)和差示扫描量热法(DSC)分析三元共聚物样品的热特性。通过傅里叶变换衰减全反射红外光谱(FTIR-ATR)对三元共聚物样品、氧化和碳化纳米纤维进行光谱表征。原始静电纺纳米纤维、氧化和碳化纳米纤维通过扫描电子显微镜(SEM)进行形貌研究。IA 的加入对三元共聚物的性能和静电纺纳米纤维有显著影响。此外,证明了氧化温度是从三元共聚物制备碳纤维的关键参数。当完成碳化过程时,所制备的纳米纤维毡的形貌和颜色都发生了变化。观察到与聚(丙烯腈-共-醋酸乙烯酯)和聚(丙烯腈-共-衣康酸)共聚物相比,聚(丙烯腈-共-醋酸乙烯酯-共-衣康酸)三元共聚物的引发温度较低,这为更容易获得碳纤维提供了机会,并且聚(丙烯腈-共-醋酸乙烯酯-共-衣康酸)三元共聚物可用作碳纤维生产的有效前驱体。