Thermosetting polyester in a sheet molding compound (SMC) shrinks by 7
to 10% and causes fiber show-through and poor surface quality. Adding
certain thermoplastics results in zero shrinkage and smooth surfaces;
these are called low-profile additives (LPA). Poly(vinyl acetate) (PV
Ac), a highly effective LPA, decreases the fracture energy from 66.3 t
o 35.1 J/m(2) when present as 14 wt% of the matrix, even though the PV
Ac is tough. It produces a nodular three dimensional network; the cros
slinked polyester nodules are interconnected by weak polyester bridges
and the PVAc forms a thin coating on each nodule. The macroscopic cro
sslinking shrinkage is offset by void formation in the PVAc phase. Cra
ck follows the void structure and cleaves the bridges between the nodu
les. Low matrix fracture toughness leads to high microcracking and ear
ly gross failure of the SMC. This paper presents alternative low profi
le additives that give excellent low profile effect with improved matr
ix fracture energy and SMC strength, Commercially available styrene-bu
tadiene block copolymers were studied. These are less polar and form d
iscrete cavitated domains of a few 100 mu m in the solid polyester mat
rix. With this morphology, good low profile and toughening usually are
contradictory, since the former requires small LPA particles for smoo
th surfaces and the latter requires large particles for crack bridging
by the rubber. However, a good compromise was found in Epoxidized Kra
ton D1300X (a 50% diblock and 50% triblock copolymer of styrene and bu
tadiene) with the compatibilizer Ricon 131MA17 (a maleic anhydride-pol
ybutadiene adduct). This produces a low profile effect equivalent to P
VAc, but with a higher matrix fracture energy of 70.7 J/m(2) and highe
r matrix modulus. With the epoxidized rubber, the flexural strength of
the SMC increases by 13% over that with PVAc, with no sacrifice of th
e modulus or strain-to-failure.