Preparation and application of aramid nanofiber via carbodiimide assisted polymerization

被引:2
|
作者
Zhang, Dongmei [1 ]
Zhang, Mingmin [2 ]
Su, Xin [1 ]
Feng, Yujun [1 ]
机构
[1] Sichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Sichuan, Peoples R China
[2] Tianjin Univ, Zhejiang Res Inst, Shaoxing 312369, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbodiimide assisted polymerization; Aramid nanofiber; Mechanical properties; Thermal properties; POLYCONDENSATION; COMPOSITES; MORPHOLOGY; BEHAVIOR; FIBERS;
D O I
10.1016/j.matdes.2024.113317
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Poly (p-phenylene terephthalamide) (PPTA), is well known as a material with excellent properties, but its application is greatly limited due to the harsh methods required for its preparation. This study proposes an innovative carbodiimide-assisted polymerization (CAP) method to simplify the synthesis process of PPTA. The eta(inh) of the prepared PPTA is 4.97 dl/g. Achieving amidation condensation at normal temperature and pressure, this method is suitable for synthesizing PPTA and allows for the recycling of the condensation reagent, offering a novel approach to green synthesis. Compared to the commercial fiber Kevlar 29, PPTA exhibits similar thermal stability, with negligible decomposition before 500 degrees C. Using the deprotonation method to prepare aramid nanofiber (ANF) resulted in various shapes of bulk materials. The ANF bulk exhibits excellent mechanical properties, with tensile and compressive strengths of 36.9 MPa and 60.68 MPa, respectively, on par with standard engineering materials. Additionally, ANF and PPTA share similar thermal stability. Furthermore, the study prepared aramid nanofiber/partially hydrolyzed polyacrylamide (ANF/HPAM) composite paper, which demonstrated outstanding mechanical performance and thermal stability. The ANF/HPAM composite paper (2% concentration of HPAM) exhibited a tensile strength of 63.32 MPa. These findings offer new insights into developing high-performance fiber materials.
引用
收藏
页数:11
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