Thin films were deposited by plasma co-polymerization of 2-isopropenyl-2-oxazoline and 1-octene, varying the total monomers flow rate and the 1-octene percentage in the mixture. The coatings wettability was evaluated by water contact angle measurements, while their stability was investigated by immersion in Phosphate Buffer Saline at 37 °C. The chemical characterization of the coatings, performed by means of Attenuated Total Reflectance Fourier Transform Infrared spectroscopy and by reaction with poly(acrylic acid), assessed a partial retention of the reactive oxazoline ring, as already observed for plasma polymerization of several oxazoline monomers alone. However, the addition of 1-octene had significant effects on the coating stability and on the surface availability of reactive oxazoline rings. Compared to those obtained by plasma polymerization of 2-isopropenyl-2-oxazoline alone, this coatings exhibited higher stability in aqueous environments but lower reactivity towards carboxylic acid groups.
Zanini, S., Lehocky, M., Lopez-Garcia, J., Riccardi, C. (2019). Plasma polymerization of 2-isopropenyl-2-oxazoline: Improvement of the coating stability by co-polymerization with 1-octene. THIN SOLID FILMS, 677, 55-61 [10.1016/j.tsf.2019.03.014].
Plasma polymerization of 2-isopropenyl-2-oxazoline: Improvement of the coating stability by co-polymerization with 1-octene
Zanini, S
;Riccardi, C
Membro del Collaboration Group
2019
Abstract
Thin films were deposited by plasma co-polymerization of 2-isopropenyl-2-oxazoline and 1-octene, varying the total monomers flow rate and the 1-octene percentage in the mixture. The coatings wettability was evaluated by water contact angle measurements, while their stability was investigated by immersion in Phosphate Buffer Saline at 37 °C. The chemical characterization of the coatings, performed by means of Attenuated Total Reflectance Fourier Transform Infrared spectroscopy and by reaction with poly(acrylic acid), assessed a partial retention of the reactive oxazoline ring, as already observed for plasma polymerization of several oxazoline monomers alone. However, the addition of 1-octene had significant effects on the coating stability and on the surface availability of reactive oxazoline rings. Compared to those obtained by plasma polymerization of 2-isopropenyl-2-oxazoline alone, this coatings exhibited higher stability in aqueous environments but lower reactivity towards carboxylic acid groups.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.