TY - JOUR
T1 - N-1-alkylitaconamic acids-co-styrene copolymers. 1. Synthesis, characterization and monomer reactivity ratios
AU - Urzúa, M.
AU - Gatica, N.
AU - Gargallo, L.
AU - Radic', D.
PY - 2000
Y1 - 2000
N2 - Copolymers containing N-1-ethylitaconamic acid, N-1-propylitaconamic acid, N-1-butylitaconamic acid, N-1-hexylitaconamic acid, N-1-octylitaconamic acid and N-1-decylitaconamic acid with styrene of different comonomer compositions were synthesized and characterized. Copolymer composition was determined by elemental analysis following the nitrogen content in the resulting copolymers. Monomer reactivity ratios r1 and r2 of the different copolymers were estimated using straight line intersection procedures such as Fineman-Ross (F-R) and Kelen-Tüdos (K-T) and by a nonlinear one, according to the reactivity ratios error-in-variables model (RREVM). Good agreement between the different procedures for r1 and r2 determination was found. Differences in the reactivity of N-1-alkylitaconamic acids (NAIA) relative to styrene were found i.e., ethyl and propyl derivative are less reactive with itself than butyl, hexyl, octyl, and decyl derivatives with itself. Copolymers with some tendency toward small block formation are found.
AB - Copolymers containing N-1-ethylitaconamic acid, N-1-propylitaconamic acid, N-1-butylitaconamic acid, N-1-hexylitaconamic acid, N-1-octylitaconamic acid and N-1-decylitaconamic acid with styrene of different comonomer compositions were synthesized and characterized. Copolymer composition was determined by elemental analysis following the nitrogen content in the resulting copolymers. Monomer reactivity ratios r1 and r2 of the different copolymers were estimated using straight line intersection procedures such as Fineman-Ross (F-R) and Kelen-Tüdos (K-T) and by a nonlinear one, according to the reactivity ratios error-in-variables model (RREVM). Good agreement between the different procedures for r1 and r2 determination was found. Differences in the reactivity of N-1-alkylitaconamic acids (NAIA) relative to styrene were found i.e., ethyl and propyl derivative are less reactive with itself than butyl, hexyl, octyl, and decyl derivatives with itself. Copolymers with some tendency toward small block formation are found.
UR - https://www.scopus.com/pages/publications/0003001714
U2 - 10.1081/MA-100101079
DO - 10.1081/MA-100101079
M3 - Article
AN - SCOPUS:0003001714
SN - 1060-1325
VL - 37 A
SP - 37
EP - 47
JO - Journal of Macromolecular Science, Part A: Pure and Applied Chemistry
JF - Journal of Macromolecular Science, Part A: Pure and Applied Chemistry
IS - 1-2
ER -