B. Sandner et al., COPOLYMERIZATION AND ACTIVATION OF PEROXIDE DECOMPOSITION WITH ACRYLIC DERIVATIVES OF TERTIARY AROMATIC-AMINES, Polymer, 35(15), 1994, pp. 3285-3289
The reactivity parameters of the copolymerization of N,N-bis(2-methacr
yloyloxyethyl)-p-toluidine (BMAT) (M1) with methyl methacrylate (MMA)
(M2) in 1,4-dioxane, i.e. r1 = 1.07 +/- 0.20, and r2 = 0.11 +/- 0.19,
and with bisphenol-A bis(2-hydroxypropyl methacrylate) (Bis-GMA) (M2)
in benzene, i.e. r1 = 0.58 +/- 0.04, and r2 = 0.03 +/- 0.03, were dete
rmined at 60-degrees-C at low concentration and low conversion (approx
imately 5%) of the monomers. Strongly delayed gelation occurred during
the copolymerization of BMAT and MMA at monomer conversions of 20-30%
, relatively independently of the composition of the monomer mixture.
The efficiency of BMAT and N-acryloyl-N'-phenylpiperazine as activator
s in the redox initiated copolymerization of Bis-GMA in dental composi
tes at ambient temperatures was found to be comparatively low. In the
case where BMAT was used in equimolar proportions to benzoyl peroxide
the former component was not detectable in the extract of the cured co
mposite.