Cationic poly(N-isopropylacrylamide) block copolymer adsorption investigated by dual polarization interferometry and lattice mean-field theory

A series of cationic diblock copolymers, poly(N-isopropylacrylamide)(48)-block-poly((3-acrylamidopropyl)trimethylammonium chloride)(X), abbreviated as PNIPAAM(48)-b-PAMPTMA(+)(X) (X = 0, 6, 10, 14, and 20), has been synthesized, and their adsorption onto silicon oxynitride from aqueous solution has...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 28(2012), 39 vom: 02. Okt., Seite 14028-38
1. Verfasser: Shovsky, Alexander (VerfasserIn)
Weitere Verfasser: Knohl, Stefan, Dedinaite, Andra, Zhu, Kaizheng, Kjøniksen, Anna-Lena, Nyström, Bo, Linse, Per, Claesson, Per M
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2012
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Acrylamides Acrylic Resins Cations Polymers Silicon Compounds poly-N-isopropylacrylamide 25189-55-3 silicon nitride QHB8T06IDK
Beschreibung
Zusammenfassung:A series of cationic diblock copolymers, poly(N-isopropylacrylamide)(48)-block-poly((3-acrylamidopropyl)trimethylammonium chloride)(X), abbreviated as PNIPAAM(48)-b-PAMPTMA(+)(X) (X = 0, 6, 10, 14, and 20), has been synthesized, and their adsorption onto silicon oxynitride from aqueous solution has been investigated using dual polarization interferometry. The polymer adsorption was modeled by using a lattice mean-field theory, and a satisfactory consistency between theory and experiments was found in terms of surface excess and layer thickness. Both theory and experiments show that the adsorption is limited by steric repulsion for X < X(max) and by electrostatic interactions for X > X(max). Modeling demonstrates that significant surface charge regulation occurs due to adsorption. Both the nonionic and cationic block exhibit nonelectrostatic affinity to silicon oxynitride and thus contribute to the driving force for adsorption, and modeling is used for clarifying how changes in the nonelectrostatic affinity affects the surface excess. The segments of the nonionic and cationic blocks seem less segregated when both have a nonelectrostatic affinity for the surface compared to the case where the segments had no surface affinity. Adsorption kinetics was investigated experimentally. Two kinetic regimes were observed: the adsorption rate is initially controlled by the mass transfer rate to the surface and at higher coverage is limited by the attachment rate
Beschreibung:Date Completed 19.02.2013
Date Revised 25.09.2018
published: Print-Electronic
Citation Status MEDLINE
ISSN:1520-5827
DOI:10.1021/la302154p