Facile hydroxylation of halloysite nanotubes for epoxy nanocomposite applications
Polymer nanocomposites have been extensively investigated over the past two decades, resulting in a wide range of applications because of their excellent performance. Halloysite, a type of naturally occurring aluminosilicate, has attracted increasing interest in polymer nanocomposite applications, e...
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Veröffentlicht in: | Polymer (Guilford) 2014-12, Vol.55 (25), p.6519-6528 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Polymer nanocomposites have been extensively investigated over the past two decades, resulting in a wide range of applications because of their excellent performance. Halloysite, a type of naturally occurring aluminosilicate, has attracted increasing interest in polymer nanocomposite applications, especially for the enhancement of mechanical properties owing to its tubular structure. Herein, we report a facile approach to achieve a high level of dispersion of halloysite nanotubes (HNTs) in epoxy by treating HNTs with a low concentration of sodium hydroxide (NaOH). The NaOH treatment resulted in the formation of hydroxyl groups on the surface of HNTs, leading to a much higher level of dispersion of HNTs in water, organic polar solvents, and epoxy matrix. The higher density of external silanol groups (Si–OH) of hydroxylated HNTs (h-HNTs) was confirmed by X-ray photoelectron spectroscopy (XPS) characterization. Such a higher level of dispersion and stronger interface led to simultaneous enhancement in both the stiffness and the toughness of epoxy/h-HNT nanocomposites. Systematic characterizations were performed to investigate the related stiffening and toughening mechanism. The implication of the present findings is discussed.
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•The halloysite nanotubes were treated with a low concentration of sodium hydroxide.•The treated halloysite showed good dispersion in polar solvents, and epoxy matrix.•The epoxy/treated halloysite nanocomposite showed enhancing mechanical properties. |
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ISSN: | 0032-3861 1873-2291 |
DOI: | 10.1016/j.polymer.2014.10.044 |