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Autor(en): Albernaz, Vanessa L.
Bach, Monika
Weber, Achim
Southan, Alexander
Tovar, Günter E. M.
Titel: Active ester containing surfmer for one-stage polymer nanoparticle surface functionalization in mini-emulsion polymerization
Erscheinungsdatum: 2018
Dokumentart: Zeitschriftenartikel
Seiten: 16, 3
Erschienen in: Polymers 10 (2018), No. 408
URI: http://elib.uni-stuttgart.de/handle/11682/10080
http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-100805
http://dx.doi.org/10.18419/opus-10063
ISSN: 2073-4360
Zusammenfassung: Functional surface active monomers (surfmers) are molecules that combine the functionalities of surface activity, polymerizability and reactive groups. This study presents an improved pathway for the synthesis of the active ester containing surfmer p-(11-acrylamido)undecanoyloxyphenyl dimethylsulfonium methyl sulfate (AUPDS). Further, the preparation of poly(methyl methacrylate) and polystyrene nanoparticles (NPs) by miniemulsion polymerization using AUPDS is investigated, leading to NPs with active ester groups on their surface. By systematically varying reaction parameters and reagent concentrations, it was found that AUPDS feed concentrations between 2-4 mol-% yielded narrowly distributed and stable spherical particles with average sizes between 83 nm and 134 nm for non-cross-linked NPs, and up to 163 nm for cross-linked NPs. By basic hydrolysis of the active ester groups in aqueous dispersion, the positive ζ-potential (ZP) was converted into a negative ZP and charge quantities determined by polyelectrolyte titrations before and after hydrolysis were in the same range, indicating that the active ester groups were indeed accessible in aqueous suspension. Increasing cross-linker amounts over 10 mol-% also led to a decrease of ZP of NPs, probably due to internalization of the AUPDS during polymerization. In conclusion, by using optimized reaction conditions, it is possible to prepare active ester functionalized NPs in one stage using AUPDS as a surfmer in miniemulsion polymerization.
Enthalten in den Sammlungen:04 Fakultät Energie-, Verfahrens- und Biotechnik

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