Abstract
Poly(methyl methacrylate-co-vinylbenzyl chloride), P(MMA-co-VBC) microfibers (with submicron diameters) of about 1 μm in size were prepared by electrospinning. Silyl-functional groups were introduced onto the P(MMA-co-VBC) microfibers templates via surface-initiated atom transfer radical polymerization of 3-(trimethoxysilyl)propyl methacrylate. The silyl groups were then converted into a silica shell, approximately 0.25 μm thick, via a reaction with tetraethoxysilane in ethanolic ammonia. Hollow silica microfibers were finally generated by thermal decomposition of the P(MMA-co-VBC) template cores. Scanning electron microscopy and transmission electron microscopy were used to characterize the intermediate products and the hollow microtubes. Fourier-transform infrared spectroscopy results indicated that the polymer cores were completely decomposed. The microfibers were characterized by X-ray photoelectron spectroscopy, X-ray diffraction and the thermal gravimetric analysis.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
