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Thermal properties of glass fiber reinforced polyamide 6 composites throughout the direct long‐fiber reinforced thermoplastic process
Author(s) -
Whitfield Thomas,
Kuboki Takashi,
Wood Jeffrey,
Ugresic Vanja,
Sathyanarayana Shyam,
Dag Koffi
Publication year - 2018
Publication title -
polymer engineering and science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 111
eISSN - 1548-2634
pISSN - 0032-3888
DOI - 10.1002/pen.24529
Subject(s) - materials science , composite material , differential scanning calorimetry , thermogravimetric analysis , thermoplastic , glass fiber , polyamide , crystallization , fiber , extrusion , isothermal process , chemical engineering , physics , engineering , thermodynamics
The direct long‐fiber reinforced thermoplastic (D‐LFT) process offers a streamlined material processing technique and decreases the degradation of the material. To ensure product consistency and process optimization, it is imperative to understand how the process sequence affects degradation and thermal properties of the material during the D‐LFT process. This study investigates variation in molecular weight and thermal properties of the glass fiber reinforced polyamide 6 (PA6) composites throughout the D‐LFT process. Viscosity number (VN) measurements, thermogravimetric analyses (TGA), and differential scanning calorimetry (DSC) analyses were performed on samples taken from different locations along the D‐LFT process. It was found that VN, which is a measure of molecular weight of the PA6 base resin, decreased throughout the processes. In contrast, TGA results suggested that apparent activation energy for decomposition increased during consecutive process stages. Non‐isothermal DSC results showed that there were no significant changes to the degree of crystallization; however, isothermal DSC results indicated that later stages of the process showed a decrease in crystallization half‐time, and the largest changes were observed in areas after the two extrusion portions of the process. POLYM. ENG. SCI., 58:46–54, 2018. © 2017 Society of Plastics Engineers