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Processing and properties of poly( p ‐phenylene benzobisthiazole)/nylon fibers
Author(s) -
Wickliffe Susan M.,
Malone Michael F.,
Farris Richard J.
Publication year - 1987
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.1987.070340306
Subject(s) - differential scanning calorimetry , poly(p phenylene) , materials science , nylon 6 , ultimate tensile strength , composite material , nylon 66 , composite number , fiber , synthetic fiber , glass transition , polymerization , young's modulus , polymer chemistry , polymer , polyamide , physics , thermodynamics
Composite fibers of poly( p ‐phenylene benzobisthiazole) (PBT) with nylons were spun from dilute acid solutions. The effects of wet‐stretching, heat treatment time, tension, and temperature on the tensile properties are reported. Nylon 6,6 and nylon 6 at several molecular weights were studied. Moduli of 40 GPa and tensile strengths of 375 MPa were achieved for 30/70 PBT/nylon composites. Heat treatment of the nylon/PBT fibers at 160–225°C for 12–19 h increased the tensile modulus by 20–50% and the tensile strength by a smaller amount. At the same time, the intrinsic viscosity of the nylons increased as much as 100%, indicating the solid‐state polymerization of the nylon. The largest tensile modulus attained is less than half the theoretical value predicted by a linear “rule of mixtures” as might be expected for an oriented molecular composite. Although differential scanning calorimetry shows a melting transition at temperatures 5–10°C higher than the pure nylons, the composite does not flow at temperatures above this transition. Sulfuric acid dissolves most of the nylon, but does not destroy the mechanical integrity of the fibers; differential scanning calorimetry indicates that the remaining fiber contains little or no nylon. The results are consistent with a microstructure consisting of a microfibrillar network of PBT, surrounded by a separate nylon phase.