TY - JOUR
T1 - Blends containing amphiphilic polymers VI. Compatibilization of N-alkylitaconamic acid-co-styrene copolymers with poly(hydroxypropyl methacrylate) and poly(4-vinylphenol)
AU - Urzua, Marcela
AU - Leiva, Angel
AU - Alegria, Luz
AU - Gargallo, Ligia
AU - Radic, Deodato
PY - 2007/7
Y1 - 2007/7
N2 - Blends containing copolymers of N-alkylitaconamic acid (NAIA) with styrene (NAIA-co-S) of two copolymer compositions, that is, 80% and 50% styrene, with poly(hydoxypropyl methacrylate (PHPM) and poly(vinyl phenol) (PVPh) were studied by differential scanning calorimetry (DSC) and Fourier Transform Infrared spectroscopy (FT-IR). The phase diagrams of Tg against blend composition show one single Tg value, which are intermediate to those of the pure components. This is interpreted as miscibility over the whole range of compositions in both systems. The Calorimetric Analysis using Gordon Taylor, Couchman, and Kwei treatments allows one to conclude that interactions between the components is favorable to the miscibility. FT-IR spectra show important displacements in the wavenumber corresponding to the carbonyl groups of the itaconamic acid moiety. This behavior is atributed to strong interaction by hydrogen bonds formation, taking into account that PHPM and PVPh are interacting polymers. FTIR analysis of the blends suggests that the driving force for miscibility is hydrogen bonds formation. The variation of the absorptions of the carbonyl groups of PNAIA and the hydroxyl groups of P4VPh allows to attribute the miscibility to weak acid-base like interactions.
AB - Blends containing copolymers of N-alkylitaconamic acid (NAIA) with styrene (NAIA-co-S) of two copolymer compositions, that is, 80% and 50% styrene, with poly(hydoxypropyl methacrylate (PHPM) and poly(vinyl phenol) (PVPh) were studied by differential scanning calorimetry (DSC) and Fourier Transform Infrared spectroscopy (FT-IR). The phase diagrams of Tg against blend composition show one single Tg value, which are intermediate to those of the pure components. This is interpreted as miscibility over the whole range of compositions in both systems. The Calorimetric Analysis using Gordon Taylor, Couchman, and Kwei treatments allows one to conclude that interactions between the components is favorable to the miscibility. FT-IR spectra show important displacements in the wavenumber corresponding to the carbonyl groups of the itaconamic acid moiety. This behavior is atributed to strong interaction by hydrogen bonds formation, taking into account that PHPM and PVPh are interacting polymers. FTIR analysis of the blends suggests that the driving force for miscibility is hydrogen bonds formation. The variation of the absorptions of the carbonyl groups of PNAIA and the hydroxyl groups of P4VPh allows to attribute the miscibility to weak acid-base like interactions.
KW - Amphiphilic polymers
KW - Functionalized polymers
KW - Hydrogen bonds
KW - Miscibility
KW - Phase behavior
KW - Poly(N-1-alkylitaconamic acids)
KW - Polymer blends
UR - https://www.scopus.com/pages/publications/34247327363
U2 - 10.1080/00914030601100706
DO - 10.1080/00914030601100706
M3 - Article
AN - SCOPUS:34247327363
SN - 0091-4037
VL - 56
SP - 687
EP - 696
JO - International Journal of Polymeric Materials and Polymeric Biomaterials
JF - International Journal of Polymeric Materials and Polymeric Biomaterials
IS - 7
ER -