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Designing novel hybrid materials by one-pot co-condensation: from hydrophobic mesoporous silica nanoparticles to superamphiphobic cotton textiles.

Authors
  • Pereira, C
  • Alves, C
  • Monteiro, A
  • Magén, C
  • Pereira, A M
  • Ibarra, A
  • Ibarra, M R
  • Tavares, P B
  • Araújo, J P
  • Blanco, G
  • Pintado, J M
  • Carvalho, A P
  • Pires, J
  • Pereira, M F R
  • Freire, C
Type
Published Article
Journal
ACS Applied Materials & Interfaces
Publisher
American Chemical Society (ACS)
Publication Date
Jul 01, 2011
Volume
3
Issue
7
Pages
2289–2299
Identifiers
DOI: 10.1021/am200220x
PMID: 21615151
Source
Medline
License
Unknown

Abstract

This work reports the synthesis and characterization of mesoporous silica nanoparticles (MSNs) functionalized with tridecafluorooctyltriethoxysilane (F13) and their in situ incorporation onto cotton textiles. The hybrid MSNs and the functional textiles were prepared by a one-pot co-condensation methodology between tetraethylorthosilicate (TEOS) and F13, with hexadecyltrimethylammonium chloride (CTAC) as the template and triethanolamine as the base. The influence of the F13 to TEOS molar ratio (1:10, 1:5 and 1:3) on the nanoparticle morphology, porosity, degree of functionalization, and hydro/oleophobic properties is discussed. The hybrid nanosilicas presented high colloidal stability and were spherical and monodispersed with average particle size of ∼45 nm. They also showed high surface areas, large pore volumes, and a wormhole-type mesoporous structure. The increase in the organosilane proportion during the co-condensation process led to a more radially branched wormhole-like mesoporosity, a decrease in the surface area, pore volume, and amount of surface silanol groups, and an enrichment of the surface with fluorocarbon moieties. These changes imparted hydrophobic and oleophobic properties to the materials, especially to that containing the highest F13 loading. Cotton textiles were coated with the F13-MSNs through an efficient and less time-consuming route. The combination between surface roughness and mesoporosity imparted by the MSNs, and the low surface energy provided by the organosilane resulted in superhydrophobic functional textiles. Moreover, the textile with the highest loading of fluorocarbon groups was superamphiphobic.

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