Synthesis and properties of Nylon 4/5 copolymers for hydrophilic fibers
Autor: | Kyeong-Suk Kang, Joon Ho Kim, Yu-Kyoung Hong, Young-Jun Kim |
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Rok vydání: | 2014 |
Předmět: |
chemistry.chemical_classification
Thermogravimetric analysis Materials science Polymers and Plastics General Chemical Engineering Comonomer General Chemistry Polymer Nylon 4 chemistry.chemical_compound Differential scanning calorimetry Polymerization chemistry Chemical engineering Polymer chemistry Copolymer Thermal stability |
Zdroj: | Fibers and Polymers. 15:1343-1348 |
ISSN: | 1875-0052 1229-9197 |
DOI: | 10.1007/s12221-014-1343-0 |
Popis: | Nylon 4, which can be synthesized by anionic ring-opening polymerization, has good mechanical properties and a very high affinity for water owing to its high polarity. On the other hand, despite its high melting temperature, the polymer has not been commercialized because of its low thermal stability. In this study, copolymerization of 2-pyrrolidone (C4) with 2-piperidone (C5) was performed to reduce the melting temperature of Nylon 4 homopolymer. The copolymerization reaction was controlled by changing the comonomer content, catalyst content, temperature, initiator content, and reaction time. The Nylon copolymers were characterized by 1H-nuclear magnetic resonance (NMR) spectroscopy, differential scanning calorimetry, and thermogravimetric analysis. The hydrophilic properties of Nylon 4 and its copolymers were evaluated by surface free energy analysis and moisture regain measurement. The intrinsic viscosity and polymerization yield of Nylon 4 increased with increasing catalyst concentration until 5 mole% and decreased with further increases in catalyst loading. The proton NMR spectrum revealed the composition of the Nylon 4/5 copolymer to be 62.5 % C4 moiety at a 5:5 comonomer feed ratio. The melting temperature of the Nylon 4/5 copolymers decreased considerably according to the composition. The moisture regain of the Nylon 4/5 copolymer was higher than 6.4 % even at 77.3 % C4 in composition. |
Databáze: | OpenAIRE |
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