Reference : Highly regular polyampholytic structures adsorbed directly from solution
Scientific journals : Article
Engineering, computing & technology : Materials science & engineering
Physical, chemical, mathematical & earth Sciences : Chemistry
http://hdl.handle.net/2268/10204
Highly regular polyampholytic structures adsorbed directly from solution
English
Mahltig, Boris [Institut für Polymerforschung, Dresden, Germany > > > >]
Müller-Buschbaum, P. [Technische Universität, München, Germany > > > >]
Wolkenhauer, M. [Max-Planck-Institut für Polymerforschung, Mainz, Germany > > > >]
Wunnicke, O. [Institut für Polymerforschung, Dresden, Germany > > > >]
Wiegand, S. [Max-Planck-Institut für Polymerforschung, Mainz, Germany > > > >]
Gohy, Jean-François [Université de Liège - ULiège > Department of Chemistry > Center for Education and Research on Macromolecules (CERM) > >]
Jérôme, Robert mailto [Université de Liège - ULiège > Department of Chemistry > Center for Education and Research on Macromolecules (CERM) > >]
Stamm, Manfred [Institut für Polymerforschung, Dresden, Germany > > > >]
1-Oct-2001
Journal of Colloid and Interface Science
Academic Press Inc Elsevier Science
242
1
36-43
Yes (verified by ORBi)
International
0021-9797
1095-7103
San Diego
CA
[en] This article concerns the adsorption of the diblock polyampholyte poly(methacrylic acid)-block-poly((dimethylamino)ethyl methary-late) (PMAA-b-PDMAEMA) from aqueous solution on silicon substrates. The investigated polyampholyte is characterized by a small molecular weight around 15,000 g/mol and a big positively charged PDMAEMA block. The adsorbed amount determined by ellipsom-etry was str ongly influenced by the pH of the adsorption solution. Using dynamic light scattering polyampholytic structures with diameters around 50 nm were found in aqueous solution. The hy-drodynamic diameter was hardly affected by changing the pH of the polymer solution. Analogous regular structures were also found by scanning force microscopy (SFM) and grazing incidence, small angle X-ray scattering (GISAXS) at the silicon surface after the adsorption process. While SFM provides a topographical image of a small part of the adsorbed polyampholytic layer; GISAXS was used to get a statistical description of the lateral surface structures. The adsorbed structures were highly regular and their sizes were nearly pH independent over a lar ge pH region. Only directly at the isoelectric point of the polyampholyte larger adsorbed structures were observed. Compared with earlier investigated PMAA-b-PDMAEMA systems we are now able to prepare highly regular polyampholytic structures at silicon surfaces. There are two kinds of interactions for the adsorbed micelles. First, the charged block of the chains is directly attracted to the substrate via electrostatic interactions, while the uncharged part of the chains is only hydrophobically attracted via the hydrophobic core of the adsorbed micelle.
Center for Education and Research on Macromolecules (CERM)
The DFG Schwerpunkt Polyelektrolyte (Grant IIC10-322 1009) ; Politique Scientifique Fédérale (Belgique) = Belgian Federal Science Policy ; The European Science Foundation Program SUPERNET
Researchers
http://hdl.handle.net/2268/10204
10.1006/jcis.2001.7771
http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6WHR-45B63PX-3N-1&_cdi=6857&_user=532038&_orig=browse&_coverDate=10%2F01%2F2001&_sk=997579998&view=c&wchp=dGLzVtb-zSkzV&md5=6ef01e3baf571458409dac6ebaa7c5b6&ie=/sdarticle.pdf
http://www.elsevier.com/wps/find/journaldescription.cws_home/622861/description#description
The authors acknowledge Journal of Colloid and Interface Science (Elsevier) for allowing them to archive this paper.

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