Morphological changes of a molten polymer/polymer interface driven by grafting

Citation
Jb. Jiao et al., Morphological changes of a molten polymer/polymer interface driven by grafting, MACROMOLEC, 32(19), 1999, pp. 6261-6269
Citations number
45
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
MACROMOLECULES
ISSN journal
00249297 → ACNP
Volume
32
Issue
19
Year of publication
1999
Pages
6261 - 6269
Database
ISI
SICI code
0024-9297(19990921)32:19<6261:MCOAMP>2.0.ZU;2-A
Abstract
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.