Whether interfacial tension between two molten polymers can be reduced sign
ificantly by the formation of copolymer at the interface by chemical reacti
on of functionalized chains is the question addressed by this paper. To ans
wer it, model experiments are carried out by grafting of benzylamine end-fu
nctionalized deuterated polystyrene (dPS-NH2) onto poly(styrene-r-maleic an
hydride) (PSMA) random copolymer at an initially planar melt interface betw
een polystyrene (PS) and PSMA. Various volume fractions of dPS-NH2 with pol
ymerization indices N = 33, 55, and 270 were mixed with PS and then reacted
with PSMA above the T-g of PS and PSMA. The interfacial excess, z*, of the
dPS portion of the graft copolymer formed at the boundary was measured usi
ng forward recoil spectrometry. The values of normalized grafting density z
*/R-g where R-g is the radius of gyration of dPS-NH2, are observed to be as
large as 40, 9, and 4 for the N = 33, 55, and 270 dPS-NH2 chains, respecti
vely. These large values signal the formation of a layer of microemulsion w
hich occurs when the interfacial tension of the flat interface is driven ne
gative by the increasing graft copolymer excess at the interface. The inter
facial instability is followed by monitoring the positions of Au particles
deposited on the original (flat) interface using cross-sectional transmissi
on electron microscopy (TEM). Evidence of the interfacial corrugation induc
ed by the instability is also available from scanning force microscopy (SFM
) of the exposed PSMA interface after selective removal of PS using a solve
nt wash. The length scale of the corrugation is around 200 nm, which is the
same magnitude as the size of the emulsion droplets shown by TEM near the
interface. The onset of the interface instability occurs at critical values
of z*/R-g of about 1.8 for N = 55 and z*/R-g of about 2.5 for N = 270 dPS-
NH2 chains. These values are predicted qualitatively by self-consistent mea
n field theory.