posted on 2018-11-14, 00:00authored byAdam J. Clancy, Hannah S. Leese, Noelia Rubio, David J. Buckley, Jake L. Greenfield, Milo S. P. Shaffer
Grafting
polymers onto single-walled carbon nanotubes (SWCNTs)
usefully alters properties but does not typically yield stable, solvated
species directly. Despite the expectation of steric stabilization,
a damaging (re)dispersion step is usually necessary. Here, poly(vinyl
acetate)s (PVAc’s) of varying molecular weights are grafted
to individualized, reduced SWCNTs at different concentrations to examine
the extent of reaction and degree of solvation. The use of higher
polymer concentrations leads to an increase in grafting ratio (weight
fraction of grafted polymer relative to the SWCNT framework), approaching
the limit of random sequentially adsorbed Flory “mushrooms”
on the surface. However, at higher polymer concentrations, a larger
percentage of SWCNTs precipitate during the reaction; an effect which
is more significant for larger weight polymers. The precipitation
is attributed to depletion interactions generated by ungrafted homopolymer
overcoming Coulombic repulsion of adjacent like-charged SWCNTs; a
simple model is proposed. Larger polymers and greater degrees of functionalization
favor stable solvation, but larger and more concentrated homopolymers
increase depletion aggregation. By using low concentrations (25 μM)
of larger molecular weight PVAc (10 kDa), up to 65% of grafted SWCNTs
were retained in solution (at 65 μg mL–1)
directly after the reaction.