147
Views
2
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis and characterization of core-shell type silica-polymer composites by surface-initiated SET-LRP

, , , , &
Pages 174-180 | Published online: 22 Nov 2017
 

ABSTRACT

A facile route for preparation of poly(tert-butyl acrylate) covalently wrapped silica nanoparticles (SiO2/PtBA) was demonstrated by the single-electron transfer mediated living radical polymerization (SET-LRP). Firstly, the surface of silica nanoparticles (SiO2 NPs) was modified with (3-aminopropyl) trimethoxysilane. Subsequently, a SET-LRP initiator was immobilized on the amine functional SiO2 NPs by the Ugi reaction of 2-bromo-2-methylpropionic acid, benzaldehyde, and 1-pentyl isocyanide. The SET-LRP of tert-butyl acrylate was carried out by using copper wire and PMDTA as a catalyst system. The grafting of PtBA on the surface of SiO2 NPs was investigated by FT-IR, XRD, TGA, and TEM analysis. Gel permeation chromatography analysis illustrated the molecular weight of PtBA increased with monomer conversion. The hydrolysis of the PtBA part yielded hydrophilic poly(acrylic acid) decorated SiO2 NPs, which showed high colloidal stability.

Funding

This work was supported by the Korea Industrial Complex Corporation Grant funded by the Ministry of Trade, Industry and Energy.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 2,387.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.