缩聚物
微尺度化学
盐(化学)
固态
材料科学
成核
界面聚合
化学工程
高分子化学
化学
热力学
有机化学
聚合物
物理化学
物理
数学教育
单体
工程类
数学
作者
Angeliki D. Mytara,Athanasios D. Porfyris,Stamatina Vouyiouka,C. D. Papaspyrides
出处
期刊:Polymers
[MDPI AG]
日期:2021-08-06
卷期号:13 (16): 2625-2625
被引量:2
标识
DOI:10.3390/polym13162625
摘要
The direct solid state polymerization (DSSP) of hexamethylene diammonium dodecanoate (PA 612 salt) was investigated for two different salt grades, fossil-based and bio-based. Aliphatic polyamide salts (such as PA 612 salt) are highly susceptible to solid melt transition (SMT) phenomena, which restrain the industrial application of DSSP. To that end, emphasis was given on reactor design, being the critical parameter influencing byproduct diffusion, amine loss and inherent DSSP kinetics. Experiments took place both at the microscale and the laboratory scale, in which two different reactors were tested in terms of bypassing SMT phenomena. The new reactor designed here proved quite successful in maintaining the solid state during the reaction. Scouting experiments were conducted in order to assess the effect of critical parameters and determine appropriate reaction conditions. Fossil-based PA 612 products proved to have a better end-group imbalance in comparison to bio-based ones, which is critical in terms of achieving high molecular weight. Finally, a real DSSP process was demonstrated, starting from PA 612 salt crystals and ending with PA 612 particles.
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