The
solubility, polymerization, and the macromolecular structure
of cured blends of BPA-based benzoxazine (BA-a) in end-group tosylated
poly(ethylene glycol) (mPEGOTs) are studied and compared to analogues
from hydroxyl-terminated poly(ethylene glycol). BA-a can be homogeneously
dispersed in both polymers where a wide loading range of ∼100–40
wt % BA-a is possible. The cure temperature for blended BA-a/mPEGOTs
was up to 50 °C less than that of pure BA-a or mPEGOH blends.
It is proposed that nucleophilic attack of BA-a on the end-group of
mPEGOTs produces free tosylate and cationic BA-a-based initiators
that act as cure catalystswhere the former was detected by
TGA-FTIR and TGA-MS. H-NMR and FTIR revealed the polybenzoxazine (PBA-a)
synthesized in mPEGOTs consists of a phenolic rich molecular structure
with H-bonded hydroxyl residues and grafted PEG-chains. SEM confirmed
that this material, P(BA-a)-graft-mPEGOTs, has a
homogeneous microstructure. The glass transition and the thermal stability
of the P(BA-a)-graft-mPEGOTs can be tuned based on
the blend composition.