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Gas phase mineralization and mesoscopic replication of polyvinyl alcohol (PVA) nanofibers represents an attractive route to the preparation of silica nanotubes and hollow fibers with independent control of pore diameter and wall size. In the sol/gel gas phase process, PVA nanofibers, produced by electrospinning of aqueous PVA, were encapsulated in a thin silica shell by repeated sequenced feed of SiCl 4 and H 2 O vapors, followed by thermal degradation of the PVA core at 550 °C. The hollow fiber wall thickness was governed by the number of SiCl 4 /H 2 O cycles with an average increase of the wall size of 0.7 nm per cycle. In contrast to conventional sol/gel electrospinning and wet sol/gel dip coating, shearing of such hollow silicate nanofibers afforded single silica nanotubes with an average length of a few microns. Aqueous silica sols added together with PVA gave control of the inner pore architectures. Methylalumoxane (MAO) activated silica nanotubes were used as supports for half sandwich chromium (III) ( Cr ) and post metallocene ( Fe ) catalysts for ethylene polymerization and in-situ nanocomposite formation with uniform dispersion of silica nanotubes within the polyethylene matrix. A blend of Cr and Fe was supported on silica nanotubes to produce melt processable polyethylene nanocomposites with bimodal molecular weight distributions. |
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