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Antistatic‐reinforced biocomposites of polyamide‐6 and polyaniline‐coated curauá fibers prepared on a pilot plant scale
Author(s) -
Araujo J.R.,
Adamo C.B.,
Costa e Silva M.V.,
Paoli M.A.
Publication year - 2013
Publication title -
polymer composites
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.577
H-Index - 82
eISSN - 1548-0569
pISSN - 0272-8397
DOI - 10.1002/pc.22516
Subject(s) - materials science , antistatic agent , composite material , polyamide , polyaniline , extrusion , ultimate tensile strength , composite number , polymer , polymerization , layer (electronics)
Curauá fibers were used with success as a reinforcing agent in polyamide‐6, however, for several applications, an antistatic dissipation property is also desirable and the incorporation of an intrinsically conducting polymer is a suitable way to promote this. The novelty of this work is the simultaneous introduction of these two properties, antistatic and reinforcement, using one filler, obtained by depositing polyaniline on the surface of short curauá fibers. Nearly 5–30 wt% of these modified fibers were dispersed by extrusion in polyamide‐6, the composites were injection molded and characterized by electrical, mechanical, morphological, and rheological properties. The tensile strength of the polyamide‐6 composites reinforced with 5 and 30 wt% of polyaniline coated curauá fibers, was 56% higher and 23% lower than the values obtained for pure polyamide‐6, respectively. Also, the composite reinforced with 5 wt% of fibers, when processed with lower shearing rates, showed conductivity in the range of antistatic materials, 4 μS cm −1 . Scanning electronic microscopy and infrared spectroscopy showed an improvement in interfacial adhesion in PA‐6/CF‐PAni composites. The composite prepared with 5 wt% of polyaniline coated curauá fibers gave the best balance between the electrical and the mechanical properties. Extrusion and injection molding methods used here are suitable for continuous large scale production. POLYM. COMPOS., 34:1081–1090, 2013. © 2013 Society of Plastics Engineers

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