Confinement and nucleation effects in poly(ethylene oxide) melt-compounded with neat and coated sepiolite nanofibers: Modulation of the structure and semicrystalline morphology

• Published in: European polymer journal Vol. 49; no. 1; pp. 118 - 129
• Main Authors: Mejía, Alberto, García, Nuria, Guzmán, Julio, Tiemblo, Pilar
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier Ltd 01.01.2013; Elsevier
• Subjects: Applied sciences; Composites; Confinement; Crystallization; Exact sciences and technology; Forms of application and semi-finished materials; Nanocomposites; Poly(ethylene oxide); Polymer industry, paints, wood; Sepiolite; Surface modification; Technology of polymers; Surface modification; Confinement; Poly(ethylene oxide); Nanocomposites; Sepiolite; Crystallization; Mixing; Transport properties; Gaseous diffusion; Coated fiber; Mineral fiber; Transformation temperature; Ethylene oxide polymer; Spherulites; Nanocomposite; Manufacturing; Clay; Crystallinity; Experimental study; Gas permeability; Melt crystallization; Dynamic mechanical properties; Morphology; Concentration effect; Growth from melt
• ISSN: 0014-3057; 1873-1945
• DOI: 10.1016/j.eurpolymj.2012.09.014

[Display omitted] ► In PEO/clay nanofibers composites, nanofibers are seen to both confine and nucleate the polymer. ► Confinement effects are better evidenced in composites prepared with coated clay nanofibers. ► Nucleation is better evidenced in composites prepared with neat clay nanofibers. ► Clay nanofibers alter the PEO crystalline lamellae orientation and so the composite tortuosity. ► Gas diffusion coefficients increase a two-fold because of the tortuosity modification. Composites have been prepared by melt compounding poly(ethylene oxide) with neat sepiolite, sepiolite coated with polyethylene glycol and with d-α-tocopherol polyethylene glycol 1000 succinate. It has been found that the nature of the sepiolite surface and its ratio in the composite enable the modulation of interfacial (nucleation) and confinement phenomena, both of which have distinct and opposed effects on the polymer’s crystalline phase. The modulation of both phenomena allows to tune the final morphology and structure of the polymer, this tuning including spherulite size, orientation of the crystalline lamellae, tortuosity of the crystalline phase, chain conformational disorder, glass transition temperature and pre-melting α′relaxation. Some of these modifications are thickness dependent, what is frequently found when the semicrystalline morphology of polymers is altered by its confinement into micrometric domains. Basic properties of the polymer such as elastic modulus and gas permeability are seen to depend very strongly on the morphology and structure modulation.