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Synthesis and Concentration of Organosols of Silver Nanoparticles Stabilized by AOT: Emulsion Versus Microemulsion

In this work, we tried to combine the advantages of microemulsion and emulsion synthesis to obtain stable concentrated organosols of Ag nanoparticles, promising liquid-phase materials. Starting reagents were successively introduced into a micellar solution of sodium bis-(2-ethylhexyl)­sulfosuccinate...

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Bibliographic Details
Published in:Langmuir 2018-02, Vol.34 (8), p.2815-2822
Main Authors: Bulavchenko, Alexander I, Arymbaeva, Aida T, Demidova, Marina G, Popovetskiy, Pavel S, Plyusnin, Pavel E, Bulavchenko, Olga A
Format: Article
Language:English
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Summary:In this work, we tried to combine the advantages of microemulsion and emulsion synthesis to obtain stable concentrated organosols of Ag nanoparticles, promising liquid-phase materials. Starting reagents were successively introduced into a micellar solution of sodium bis-(2-ethylhexyl)­sulfosuccinate (AOT) in n-decane in the dynamic reverse emulsion mode. During the contact of the phases, Ag+ passes into micelles and Na+ passes into emulsion microdroplets through the cation exchange AOTNaOrg + AgNO3 Aq = AOTAgOrg + NaNO3 Aq. High concentrations of NaNO3 and hydrazine in the microdroplets favor an osmotic outflow of water from the micelles, which reduces their polar cavities to ∼2 nm. As a result, silver ions are contained in the micelles, and the reducing agent is present mostly in emulsion microdroplets. The reagents interact in the polar cavities of micelles to form ∼7 nm Ag nanoparticles. The produced nanoparticles are positively charged, which permitted their electrophoretic concentration to obtain liquid concentrates (up to 30% Ag) and a solid Ag–AOT composite (up to 75% Ag). Their treatment at 250 °C leads to the formation of conductive films (180 mOhm per square). The developed technique makes it possible to increase the productivity of the process by ∼30 times and opens up new avenues of practical application for the well-studied microemulsion synthesis.
ISSN:0743-7463
1520-5827
DOI:10.1021/acs.langmuir.7b04071