Publication | Open Access
Electrostatically Driven Coassembly of a Diblock Copolymer and an Oppositely Charged Homopolymer in Aqueous Solutions
53
Citations
16
References
2007
Year
EngineeringChemistrySoft MatterCorona BlockAcrylic AcidDriven CoassemblyGuinier RadiusBiophysicsPolymer ChemistryMaterials ScienceDiblock CopolymerMicelleMolecular EngineeringAqueous SolutionsColloidal SystemBlock Co-polymersPolymer SolutionDepolymerizationSelf-assemblyPolymer SciencePolymer Self-assembly
Electrostatically driven coassembly of poly(acrylic acid)-block-poly(acrylamide), PAA-b-PAAm, and poly(2-methylvinylpyridinium iodide), P2MVP, leads to formation of micelles in aqueous solutions. Light scattering and small angle neutron scattering experiments have been performed to study the effect of concentration and length of the corona block (NPAAm = 97, 208, and 417) on micellar characteristics. Small angle neutron scattering curves were analyzed by generalized indirect Fourier transformation and model fitting. All scattering curves could be well described with a combination of a form factor for polydisperse spheres in combination with a hard sphere structure factor for the highest concentrations. Micellar aggregation numbers, shape, and internal structure are relatively independent of concentration for Cp < 23.12 g L-1. The Guinier radius, average micellar radius, hydrodynamic radius, and polydispersity were found to increase with increasing NPAAm. Micellar mass and aggregation number were found to decrease with increasing NPAAm.
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