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Closed Access item Polyelectrolyte Multilayers Containing Triblock Copolymers of Different Charge Ratio

Authors:Guzman, Eduardo
San Miguel, Veronica
Peinado, Carmen
Ortega, Francisco
Rubio, Ramon G
Issue Date:2010
Publisher:American Chemical Society
Citation:Langmuir 26 (13) : 11494–11502 (2010)
Abstract:Multilayers formed by the sodium salt of poly(4-styrenesulfonate), PSS, and triblock copolymers of the form PDMAEMA-PCL-PDMAEMA (PDMAEMA corresponding to poly[2-(N,N-dimethylamino)ethyl methacrylate), and PCL, to poly(epsilon-caprolactone) have been built by layer-by-layer self-assembly from the aqueous polyelectrolyte solutions. Two types of block copolymers have been used which differ on the type of the amino groups, either hydrochloride or quaternized. This leads to changes in the charge density of the chains for the same content of amino groups. The growth of the multilayers has been followed using dissipative quartz crystal microbalance and ellipsometry techniques. The results show that, independently of the conditions used in the assembling, the film thickness grows linearly with the number of layers. The comparison of the thickness values obtained from D-QCM and ellipsometry has allowed us to calculate the water content of the polymer film. The analysis of the D-QCM data also provides the shear modulus, whose values are typical of a rubber-like polymer system. The analysis of the mass adsorbed calculated by the ellipsometric measurements indicated that the nature of the charge compensation mechanism is extrinsic for all the studied systems, although the degree of extrinsic compensation is strongly dependent on the copolymer used and the concentration in solution. Finally, it was found that the adsorption kinetic of the layers is bimodal for all the films built. Even though the characteristic adsorption times depend on the specific copolymer used, no dependence on the number of layers has been found for a given multilayer
Publisher version (URL):http://dx.doi.org/10.1021/la101043z
URI:http://hdl.handle.net/10261/57815
ISSN:0743-7463
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Appears in Collections:(ICTP) Artículos

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