Synthesis and Thermomechanical Characterization of Nylon 6/Cu Nanocomposites Produced by an Ultrasound-Assisted Extrusion Method

Author:

Sierra-Ávila Rubén1ORCID,Pérez-Alvarez Marissa2ORCID,Valdez-Garza Janett1,Avila-Orta Carlos Alberto1ORCID,Jiménez-Regalado Enrique Javier1ORCID,Mata-Padilla José M.3ORCID,Soto-Castruita Enrique2,Cadenas-Pliego Gregorio1ORCID

Affiliation:

1. Centro de Investigación en Química Aplicada, Blvd. Enrique Reyna 140, 25294 Saltillo, Coahuila, Mexico

2. CONACyT Research Fellow, Instituto Mexicano del Petróleo, Eje Central Lázaro Cárdenas Norte 152, 07730 Ciudad de México, Mexico

3. CONACyT Research Fellow, Centro de Investigación en Química Aplicada, 25294 Saltillo, Mexico

Abstract

A nylon 6 nanocomposite with copper nanoparticles processed by ultrasound-assisted extrusion was prepared at concentrations between 0.01 and 0.50 wt.%, and its thermal and mechanical properties were determined. The presence of the crystalline phase α (α1 and α2) in the polymer matrix was confirmed by X-ray diffraction, and the presence of the α2 phase showed a greater increase than the α1 phase as a function of the copper nanoparticle concentration. This process was attributed to secondary crystallization. Furthermore, it was determined that the chemical composition of the nanoparticles is a blend of metallic copper and cupric oxide. The formation of copper nanowires was observed by scanning electron microscopy, and the concentration of 0.10% exhibited the best dispersion in comparison with the other concentrations. The melting temperature of the nanocomposites underwent a slight decrease in comparison with the nylon 6, while thermal stability, crystallization temperature, and crystallinity were increased in relation to the pure polymer. This behavior is attributed to an efficient dispersion of the nanoparticles and to their functionality as crystal nucleation sites. For the 0.10% concentration nanocomposite, higher mechanical properties were obtained; tensile strength increased by 8.9%, and the tensile modulus increased by 25.4%; as a consequence, elongation at break was 62% less than that of the polymer matrix.

Funder

CONACYT/Innovate UK

Publisher

Hindawi Limited

Subject

General Engineering,General Materials Science

Reference51 articles.

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