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Title: Novel Diblock Copolymer-Grafted Multiwalled Carbon Nanotubes via a combination of Living and Controlled/Living Surface Polymerizations

Journal Article · · Journal of Polymer Science, Part A: Polymer Chemistry
DOI:https://doi.org/10.1002/pola.23865· OSTI ID:1009940
 [1];  [1];  [2];  [3]
  1. ORNL
  2. University of Tennessee, Knoxville (UTK)
  3. University of Athens, Athens, Greece

Diels Alder cycloaddition reactions were used to functionalize multiwalled carbon nanotubes (MWNTs) with 1-benzocylcobutene-10-phenylethylene (BCB-PE) or 4-hydroxyethylbenzocyclobutene (BCB-EO). The covalent functionalization of the nanotubes with these initiator precursors was verified by FTIR and thermogravimetric analysis (TGA). After appropriate transformations/additions, the functionalized MWNTs were used for surface initiated anionic and ring opening polymerizations of ethylene oxide and e-caprolactone (e-CL), respectively. The OH-end groups were transformed to isopropylbromide groups by reaction with 2-bromoisobutyryl bromide, for subsequent atom transfer radical polymerization of styrene or 2-dimethylaminoethyl methacrylate to afford the final diblock copolymers. 1H NMR, differential scanning calorimetry (DSC), TGA, and transmission electron microscopy (TEM) were used for the characterization of the nanocomposite materials. TEM images showed the presence of a polymer layer around the MWNTs as well as the dissociation of MWNT bundles. Consequently, this general methodology, employing combinations of different polymerization techniques, increases the diversity of diblocks that can be grafted from MWNTs.

Research Organization:
Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
DOE Contract Number:
DE-AC05-00OR22725
OSTI ID:
1009940
Journal Information:
Journal of Polymer Science, Part A: Polymer Chemistry, Vol. 48, Issue 5; ISSN 0887-624X
Country of Publication:
United States
Language:
English