Synthesis by emulsion polymerization of poly(butyl acrylate-co-silver acrylate) ionomers and evaluation of their possible applications

H. R. Acevedo-Parra, M. R. Torres-Vitela, M. M. Castillo-Ortega, F. Bautista, J. E. Puig, S. M. Nuño-Donlucas*

*Autor correspondiente de este trabajo

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

2 Citas (Scopus)

Resumen

The synthesis by emulsion polymerization and the characterization by a battery of techniques of poly(butyl acrylate-co-silver acrylate) [poly(BuAc-co-AgAc)] ionomers are reported here. Reaction rates were fast and conversions around 90% were obtained in less than one hour, regardless of the initial ratio of butyl acrylate and silver acrylate employed (BuAc/AgAc = 90/10, 80/20, 70/30). Particle size was in the range of 176 to 200nm, depending on the BuAc/AgAc ratio. Ionomers formation was corroborated by infrared spectroscopy and inferred by differential scanning calorimetry (DSC). DSC disclosed that the poly(BuAc-co-AgAc) has two glass transition temperatures: one at ca. 49C due to relaxation of the ionomer backbone domains rich in BuAc and another ca. 35C due to the relaxation of the backbone domains where the AgAc-units content was higher. Young moduli increased as the copolymers became richer in AgAc. Antibacterial tests against Escherichia coli with the 90/10 (BuAc/AgAc) ionomer revealed that the bacteria population diminishes from 5 log CFU/mL to less than 0.3 MPN/mL after one hour of contact with the ionomers. Also, we demonstrated that the ionomers are excellent compatibilizers for making semiconductive films of n-dodecylbenzene sulfonic acid-doped polyaniline (PANIDBSA)-poly(BuAc-co- AgAc) and poly(n-butyl methacrylate) (PBMA) blends. The electrical conductivity of the blend films, which were homogeneous, rose as the AgAc content in the films increased.

Idioma originalInglés
Páginas (desde-hasta)876-884
Número de páginas9
PublicaciónJournal of Macromolecular Science, Part A: Pure and Applied Chemistry
Volumen49
N.º10
DOI
EstadoPublicada - 1 oct. 2012

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