Polymer Brushes on Single-Walled Carbon Nanotubes by Atom Transfer Radical Polymerization of n-Butyl Methacrylate

Abstract

Polymer brushes with single-walled carbon nanotubes (SWNT) as backbones were synthesized by grafting n-butyl methacrylate (nBMA) from the ends and sidewalls of SWNT via atom transfer radical polymerization (ATRP). Carboxylic acid groups on SWNT were formed by nitric acid oxidation. The ATRP initiators were covalently attached to the SWNT by esterification of 2-hydroxyethyl 2'-bromopropionate with carboxylic acid groups. Methyl 2-bromopropionate (MBP) was added as free initiator during the brush preparation to control growth of the brushes and to monitor the polymerization kinetics. Size-exclusion chromatography (SEC) results show that the molecular weight of free poly(n-butyl methacrylate) (PnBMA) increased linearly with nBMA monomer conversion. PnBMA cleaved from the SWNT after high conversion had the same molecular weight as PnBMA produced in solution. Thermogravimetric analyses (TGA) show that the amount of PnBMA grown from the SWNT increased linearly with the molecular weight of the free PnBMA. The most highly PnBMA-functionalized SWNT dissolve in 1,2-dichlorobenzene, chloroform, and tetrahydrofuran, and solubility increases with the amount of PnBMA bound to SWNT. Near-infrared and Raman spectra indicate that the side walls of the SWNT were lightly functionalized by the nitric acid treatment and that the degree of functionalization of the SWNT did not change significantly during the formation of initiator or during the polymerization. Atomic force microscopy (AFM) images show contour lengths of the SWNT brushes on a mica surface from 200 nm to 2.0 microm and an average height of the backbone of 2-3 nm, indicating that the bundles of original SWNT were broken into individual tubes by functionalization and polymerization.