This paper describes a new method for rubber toughening brittle powder
coatings. The design involves the use of toughening agents with speci
fic physical and chemical properties. The modifiers arc low-to-medium
molecular weight polymers with polymerizable end groups (macromonomers
), To achieve the physical properties required for fabrication into fi
ne powders for subsequent deposition using conventional powder coating
equipment, semi-crystalline polymers with T(g)'s well below room temp
erature and melting points above approximately 70-degrees-C were requi
red. Upon copolymerization with a thermosetting resin, crystallization
of the modifier was precluded provided that low ethylene oxide compos
itions were employed. This scheme, in principle, yields an amorphous l
ow T(g) modifier chemically bound to the cured network. Poly(ethylene
oxide), PEO, was found to be an excellent candidate, since it has a T(
g) of -68-degrees-C and a T(m) of 70-degrees-C, sufficient crystallini
ty for friability and functional end groups for copolymerization. Free
radical polymerization of 2,2-bis[4-vinylbenzoyloxyphenyl] hexanuorop
ropane and step-growth polymerization of 4,4'-(hexafluoroisopropyliden
e)diphenyl cyanate were utilized to demonstrate the feasibility of thi
s approach. An electrostatic powder coater was used to co-deposit the
PEO macromonomers with either of the thermosetting precursor monomers,
followed by thermal curing to produce the modified networks. The resu
lting networks showed multiphase morphologies with improved toughness.