Self-Assembled Polyoxometalates Nanoparticles as Pickering Emulsion Stabilizers

被引:23
作者
Leclercq, Loic [1 ]
Mouret, Adrien [1 ]
Renaudineau, Severine [2 ]
Schmitt, Veronique [3 ]
Proust, Anna [2 ]
Nardello-Rataj, Veronique [1 ]
机构
[1] Univ Lille Sci & Technol, UCCS, CNRS, UMR 8181, F-59655 Villeneuve Dascq, France
[2] Univ Paris 06, Sorbonne Univ, UMR CNRS 8332, Inst Parisien Chim Mol, F-75005 Paris, France
[3] Univ Bordeaux, UPR CNRS 8641, Ctr Rech Paul Pascal, F-33600 Pessac, France
关键词
ULTRA-DEEP DESULFURIZATION; BOTTOM-UP APPROACH; INTERFACIAL PROPERTIES; SELECTIVE OXIDATION; MOLECULAR TECTONICS; CATALYSIS; LIQUID; SURFACTANTS; KEGGIN; ANION;
D O I
10.1021/acs.jpcb.5b01805
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We easily produced a series of polyoxometalate (POM) nanoparticles by taking benefit from electrostatic attractions between various POMs , and alkylammonium cations. These self-assembled supramolecular nanoparticles are fully characterized in terms of shape, nanostructure, and physicochemical properties. The nanoparticle differences are discussed on the basis of the chemical composition of the initial POM. Moreover, such particles have the ability to stabilize water-in-oil Pickering emulsions. Using a gel-trapping technique coupled to atomic force microscopy (AFM) observations, we determined their affinity toward oil by the contact angle of adsorbed nanoparticles: We show that the emulsion droplet size and stability can be directly linked to the nanoparticle hydrophobicity, which is tuned by the charge localization and molecular packing of POMs with the ammonium cations. Such particles are of special interest as they open large possibilities for Pickering interfacial catalysis.
引用
收藏
页码:6326 / 6337
页数:12
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