...
首页> 外文期刊>Journal of Applied Polymer Science >Phase behavior and mechanism of formation of protofiber morphology of solution spun poly(acrylonitrile) copolymers in DMF-water system
【24h】

Phase behavior and mechanism of formation of protofiber morphology of solution spun poly(acrylonitrile) copolymers in DMF-water system

机译:DMF-水体系中溶液纺丝聚丙烯腈共聚物的相行为和形成原生纤维形态的机理

获取原文
获取原文并翻译 | 示例

摘要

Phase diagrams of a series of copolymers of acrylonitrile (AN) and acrylic acid (AAc) were constructed using linearized cloud point correlation. The miscibility region in the phase diagram was found to increase with the increase in AAc content of the copolymers. For various compositions, π_(13) (polymer-water interaction parameter) values were estimated by sorption experiment. As the hydrophilic nature of the polymer increased with the increase in the content of acrylic acid, the π_(13) interaction parameter was found to decrease from poly(acrylonitrile) homopolymer to its copolymer with 50 mol % acrylic acid (AA50B). The polymer-solvent interaction parameters (π_(23)) and composition at the critical points for all the polymers were determined by fitting the theoretical bimodal curves to the experimental cloud point curves using Kenji Kamide equations. The polymer composition at the critical point was found to increase by 400% with increasing AAc content. The polymers were solution spun in DMF-water coagulation bath at 30°C and their protofiber structures were investigated under scanning electron microscopy. The observed morphological differences in protofibers were explained on the changes brought about in the phase separation behavior of the polymer-solvent-nonsolvent systems. The copolymers with higher acrylic acid content could be solution spun into void free homogeneous fibers even at conditions that produced void-filled inhomogeneous fibers in poly(acrylonitrile) and its copolymers with lower AAc content. The experiments demonstrate the important role of thermodynamics in deciding the protofiber morphology during coagulation process.
机译:使用线性浊点相关性构建了一系列丙烯腈(AN)和丙烯酸(AAc)共聚物的相图。发现相图中的可混溶区域随着共聚物中AAc含量的增加而增加。对于各种组成,通过吸附实验估算π_(13)(聚合物-水相互作用参数)值。随着聚合物的亲水性随丙烯酸含量的增加而增加,发现π_(13)相互作用参数从聚(丙烯腈)均聚物向其与50 mol%丙烯酸(AA50B)的共聚物降低。通过使用Kenji Kamide方程将理论双峰曲线拟合到实验浊点曲线,可以确定所有聚合物的聚合物-溶剂相互作用参数(π_(23))和组成。发现在临界点处的聚合物组成随着AAc含量的增加而增加400%。将聚合物在30°C的DMF-水混凝浴中溶液纺丝,并在扫描电子显微镜下研究其原纤维结构。观察到的原纤维形态差异是由聚合物-溶剂-非溶剂体系的相分离行为所引起的变化解释的。具有较高丙烯酸含量的共聚物即使在会在聚(丙烯腈)及其较低AAc含量的共聚物中产生空隙填充的不均匀纤维的条件下,也可以溶液纺成无空隙的均质纤维。实验证明了热力学在决定凝固过程中原纤维形态方面的重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号