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Synthesis and characterization of the feed ratio of polyethylene oxide (0 ∼ 10 wt % PEO) in the nylon‐6/PEO copolymer system
Author(s) -
Tseng YuChi,
Rwei SyangPeng
Publication year - 2011
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.34653
Subject(s) - materials science , copolymer , differential scanning calorimetry , polymer chemistry , fourier transform infrared spectroscopy , crystallization , dynamic mechanical analysis , ultimate tensile strength , crystallinity , izod impact strength test , composite material , chemical engineering , polymer , physics , engineering , thermodynamics
In this work, we have synthesis nylon‐6/polyethylene oxide (PEO) copolymer system based on feed ratio of PEO (0∼ 10 wt %) through condensation polymerization in a pilot scale. The structure of copolymer was confirmed by Fourier transform infrared (FTIR) spectroscopy and verified by 1 H nuclear magnetic resonance ( 1 HNMR). The thermal properties were investigated by differential scanning calorimetry (DSC) and indicated both melting temperature ( T m ) and cold crystallization temperature ( T c ) appearing unapparent decreased while increased PEO content in copolymers. The incorporation of PEO into the nylon‐6 chain reduced its tensile strength, modulus, and heat distortion temperature (HDT). The notched Izod impact strength of and ductility of the copolymers improved significantly as the PEO content was increased. The plasticizing effect was caused by the soft segments from PEO, which increases the mobility of the molecular chain in the copolymers. The results of mechanical tests agree closely with dynamic mechanical analysis (DMA) measurements. A rheological investigation revealed that neat nylon‐6 and its copolymer displayed similar behavior. The crystalline structure was examined by wide‐angle X‐ray diffraction (WAXD). The results demonstrate that the addition of a little PEO altered the crystallization from the α form to the γ form, mainly owing to the breaking parts of the original H‐bonds by the incorporation of ether groups. A mechanism of interaction between the amide and the ether group in nylon‐6/PEO copolymers is proposed. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011