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Optimising crystallisation during rapid prototyping of Fe3O4-PA6 polymer nanocomposite component.

Gupta, Ranjeetkumar; Njuguna, James; Pancholi, Ketan

Authors



Abstract

Polymer components capable of self-healing can rapidly be manufactured by injecting the monomer (ε-caprolactam), activator and catalyst mixed with a small amount of magnetic nanoparticles into a steel mould. The anionic polymerisation of the monomer produces a polymer component capturing magnetic nanoparticles in a dispersed state. Any microcracks developed in this nanocomposite component can be healed by exposing it to an external alternating magnetic field. Due to the magnetocaloric effect, the nanoparticles locally melt the polymer in response to the magnetic field and fill the cracks, but the nanoparticles require establishing a network within the matrix of the polymer through effective dispersion for functional and uniform melting. The dispersed nanoparticles, however, affect the degree of crystallinity of the polymer depending on the radius of gyration of the polymer chain and the diameter of the magnetic nanoparticle agglomerates. The variation in the degree of crystallinity and crystallite size induced by nanoparticles can affect the melting temperature as well as its mechanical strength after testing for applications, such as stimuli-based self-healing. In the case of in situ synthesis of the polyamide-6 (PA6) magnetic nanocomposite (PMC), there is an opportunity to alter the degree of crystallinity and crystallite size by optimising the catalyst and activator concentration in the monomer. This optimisation method offers an opportunity to tune the crystallinity and, thus, the properties of PMC, which otherwise can be affected by the addition of nanoparticles. To study the effect of the concentration of the catalyst and activator on thermal properties, the degree of crystallinity and the crystallite size of the component (PMC), the ratio of activator and catalyst is varied during the anionic polymerisation of ε-caprolactam, but the concentration of Fe3O4 nanoparticles is kept constant at 1 wt%. Differential Scanning Calorimetry (DSC), Fourier-transform infrared spectroscopy (FTIR), XRD (X-ray diffraction) and Thermogravimetric analysis (TGA) were used to find the required concentration of the activator and catalyst for optimum properties. It was observed that the sample with 30% N-acetyl caprolactam (NACL) (with 50% EtMgBr) among all of the samples was most suitable to Rapid Prototype the PMC dog-bone sample with the desired degree of crystallinity and required formability.

Citation

GUPTA, R., NJUGUNA, J. and PANCHOLI, K. 2022. Optimising crystallisation during rapid prototyping of Fe3O4-PA6 polymer nanocomposite component. Journal of composites science [online], 6(3), article 83. Available from: https://doi.org/10.3390/jcs6030083

Journal Article Type Article
Acceptance Date Mar 1, 2022
Online Publication Date Mar 7, 2022
Publication Date Mar 31, 2022
Deposit Date Mar 10, 2022
Publicly Available Date Mar 10, 2022
Journal Journal of Composites Science
Electronic ISSN 2504-477X
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 6
Issue 3
Article Number 83
DOI https://doi.org/10.3390/jcs6030083
Keywords Degree of crystallinity; Polyamide-6; Rapid prototyping; Nanocomposite; Self-healing
Public URL https://rgu-repository.worktribe.com/output/1615854
Related Public URLs https://rgu-repository.worktribe.com/output/1615987

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Copyright Statement
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).





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