dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:22:55Z
dc.date.accessioned2022-10-05T13:09:04Z
dc.date.available2014-05-20T13:22:55Z
dc.date.available2022-10-05T13:09:04Z
dc.date.created2014-05-20T13:22:55Z
dc.date.issued2004-06-03
dc.identifierJournal of Physical Chemistry B. Washington: Amer Chemical Soc, v. 108, n. 22, p. 7033-7039, 2004.
dc.identifier1520-6106
dc.identifierhttp://hdl.handle.net/11449/6808
dc.identifier10.1021/jp049778n
dc.identifierWOS:000221700300023
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3883862
dc.description.abstractPoly(styrene-co-methyl methacrylate) (PS-PMMA) ionomers with several degrees of sulfonation were synthesized and characterized by infrared, UV-vis, and NMR spectroscopies, elemental analysis, and differential scanning calorimetry (DSC). Stable Langmuir films could be produced with PS-PMMA with 3 and 6 mol % of sulfonation, while PS-PMMA 8% exhibited material loss to the water subphase, probably due to its higher solubility. Surface pressure and surface potential isotherms with PS-PMMA 3% spread onto salt-containing subphases pointed to a film behavior characteristic of the polyelectrolyte effect, where charge repulsion governs the film properties. The Langmuir-Blodgett films of this ionomer were successfully transferred onto various substrates, as confirmed by UV-vis and FTIR spectroscopies. Using cycling voltammetry, we show that LB films from PS-PMMA 3% can be applied in selective sensing of dopamine, even in the presence of interferents such as ascorbic acid.
dc.languageeng
dc.publisherAmer Chemical Soc
dc.relationJournal of Physical Chemistry B
dc.relation3.146
dc.relation1,331
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.titleSynthesis of poly(styrene-co-methyl methacrylate)-based ionomers and their Langmuir and Langmuir-Blodgett (LB) film formation
dc.typeArtigo


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