Polypropylene (PP) was functionalized with acrylic acid IAA) and styrene (s
t) as a comonomer by means of a radical-initiated melt-grafting reaction. F
TTR, ESCA, and H-1-NMR spectroscopies were used to characterize the formati
on of polypropylene grafted with acrylic acid (PP-g-AA) and polypropylene g
rafted with acrylic acid and styrene (PP-g-AAst). The content of AA grafted
onto PP was determined by using volumetric titration. Blends of PP with 0-
100 wt % of PP-g-AA were prepared by melt mixing. The effect of the modifie
d polymer content on the surfaces of cast films was characterized through F
TIR-ATR and ESCA analysis as well as contact-angle, wetting tension, and in
k-adhesion measurements. The influence of the content, of AA on the melting
and crystallization temperature of PP was investigated by DSC. The contact
angles of water on cast-film surfaces of PP/PF-g-AA blends decreases with
increasing modified polymer content and decreasing PP-g-AA molecular weight
. A notorious improvement on wetting tension was observed with increasing m
odified polymer content and decreasing PP-g-AA molecular weight. From FTIR-
ATR and ESCA spectra of the blends, a calculation was made of the carbonyl
index on the films' surfaces. It was found that the higher the carbonyl ind
ex, the lower the contact-angle value for the polypropylene blends. An incr
ease in crystallization temperature of PP was observed when AA monomers wer
e grafted into PP and with increasing PP-g-AA content in the blend, probabl
y caused by a nucleation effect, of AA monomers that would improve the crys
tallization capability of PP. (C) 2000 John Wiley & Sons, Inc.