Zobrazit minimální záznam

dc.contributor.authorPraus, Petr
dc.contributor.authorDvorský, Richard
dc.contributor.authorHorínková, Petra
dc.contributor.authorPospíšil, Miroslav
dc.contributor.authorKovář, Petr
dc.date.accessioned2012-07-30T11:13:57Z
dc.date.available2012-07-30T11:13:57Z
dc.date.issued2012
dc.identifier.citationJournal of Colloid and Interface Science. 2012, vol. 377, issue 1, p. 58-63.cs
dc.identifier.issn0021-9797
dc.identifier.urihttp://hdl.handle.net/10084/94924
dc.description.abstractZnS nanoparticles were precipitated in aqueous dispersions of cationic surfactant cetyltrimethylammonium bromide (CTAB). The sphere radii of ZnS nanoparticles calculated by using band-gap energies steeply decreased from 4.5 nm to 2.2 nm within CTAB concentrations of 0.4–1.5 mmol L−1. Above the concentration of 1.5 mmol L−1, the radii were stabilized at R = 2.0 nm and increased up to R = 2.5 nm after 24 h. The hydrodynamic diameters of CTAB–ZnS structures observed by the dynamic light scattering (DLS) method ranged from 130 nm to 23 nm depending on CTAB concentrations of 0.5–1.5 mmol L−1. The complex structures were observed by transmission electron microscopy (TEM). At the higher CTAB concentrations, ZnS nanoparticles were surrounded by CTA+ bilayers forming positively charged micelles with the diameter of 10 nm. The positive zeta-potentials of the micelles and their agglomerates were from 16 mV to 33 mV. Wurtzite and sphalerite nanoparticles with R = 2.0 nm and 2.5 nm covered by CTA+ were modeled with and without water. Calculated sublimation energies confirmed that a bilayer arrangement of CTA+ on the ZnS nanoparticles was preferred to a monolayer.cs
dc.language.isoencs
dc.publisherElseviercs
dc.relation.ispartofseriesJournal of Colloid and Interface Sciencecs
dc.relation.urihttps://doi.org/10.1016/j.jcis.2012.03.073cs
dc.subjectZnS nanoparticlescs
dc.subjectCetyltrimethylammonium bromidecs
dc.subjectmolecular modelingcs
dc.titlePrecipitation, stabilization and molecular modeling of ZnS nanoparticles in the presence of cetyltrimethylammonium bromidecs
dc.typearticlecs
dc.identifier.locationNení ve fondu ÚKcs
dc.identifier.doi10.1016/j.jcis.2012.03.073
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume377cs
dc.description.issue1cs
dc.description.lastpage63cs
dc.description.firstpage58cs
dc.identifier.wos000304432400009


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