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Multilayers of Weak Polyelectrolytes of Low and High Molecular Mass Assembled on Polypropylene and Self-Assembled Hydrophobic Surfaces

Year: 2011

Journal: Langmuir, 2011, 27 (8), pp 4541–4550, 20110525

Authors: Liu X. †, Goli K.K. ‡, Genzer J. ‡, Rojas O.J. *†§

Last authors: Orlando J. Rojas

Organizations: †Department of Forest Biomaterials and ‡Department of Chemical and Bimolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, United States § Faculty of Chemistry and Materials Sciences, Department of Forest Products Technology, Aalto University, Espoo, Finland

Country: Finland, USA, US, United States, United States of America, America

Hydrophobic self-assembled octadecyltrichlorosilane (ODTS), ultrathin films of polypropylene, and ODTS modified with cationic dioctadecyldimethylammonium bromide are employed as substrates for deposition of multilayers of poly(allylamine hydrochloride) and poly(acrylic acid) from aqueous solution. The assembly of highly dissipative polyelectrolyte multilayers (PEMs) is demonstrated by quartz crystal microgravimetry. The initial rate of adsorption is faster and the adsorbed amount larger on the cationic surface, while the detailed structure of the PEMs, as determined by atomic force microscopy imaging, is related primarily to the molecular weight of the adsorbing polymers. A more extensive PEM adsorption on the hydrophobic surfaces takes place with increasing ionic strength of the background electrolyte solution. The water contact angle depends on the type of polymer adsorbed as the outermost layer, indicating that, despite the expected interdifusion for the different polymer chains, there is a net macromolecular segregation to the free surface. Surface modification with the high molecular weight PEMs produces a more marked reduction of the hydrophilicity of the substrate.