High stability under extreme condition of the poly(vinyl alcohol) nanofibers crosslinked by glutaraldehyde in organic medium

Water-soluble poly(vinyl alcohol) (PVA) nanofibers cannot be applied in aqueous condition. Fortunately, the PVA nanofibers can become stable in aqueous condition after physically or chemically crosslinked. However, these crosslinking methods require some harsh experimental conditions. In this articl...

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Veröffentlicht in:Polymer degradation and stability 2017-03, Vol.137, p.229-237
Hauptverfasser: Li, Yanbao, Yao, Song
Format: Artikel
Sprache:eng
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Zusammenfassung:Water-soluble poly(vinyl alcohol) (PVA) nanofibers cannot be applied in aqueous condition. Fortunately, the PVA nanofibers can become stable in aqueous condition after physically or chemically crosslinked. However, these crosslinking methods require some harsh experimental conditions. In this article, organic solvents were introduced as the media to crosslink PVA nanofibers with glutaraldehyde, which is different from the conventional crosslinking method. The results of the field emission scanning electron microscopy (FESEM) show that the crosslinked PVA nanofibers can maintain the morphology not only in water but also in extreme solutions (such as hot water for 2 d, strong acid/alkaline solutions at 95 °C for 2 h). The tensile strength of the crosslinked PVA nanofiber mats can maintain more than 12.1 ± 1.1 MPa after soaked into these extreme solutions. The crosslinked PVA nanofiber mats with high stability and porous morphology have potential applications as filter membrane and adsorbing material. The stability of the popular poly(vinyl alcohol) nanofibers has been improved highly after crosslinked by glutaraldehyde in organic medium. The crosslinked PVA nanofibers can maintain the morphology not only in water but also in extreme solutions (such as hot water for 2 d, strong acid/alkaline solutions at 95 °C for 2 h). The crosslinked PVA nanofiber mats with high stability and porous morphology have potential applications as filter membrane and adsorbing material. [Display omitted]
ISSN:0141-3910
1873-2321
DOI:10.1016/j.polymdegradstab.2017.01.018