Aging of TiO2 nanocomposites used in sunscreen. Dispersion and fate of the degradation products in aqueous environment
2010
Labille, Jérôme | Feng, Jinghuan | Botta, Céline | Borschneck, Daniel | Sammut, Magali | Cabié, Martiane | Auffan, Melanie | Rose, Jérôme | Bottero, Jean-Yves | Centre Européen de Recherche et d'Enseignement des Géosciences de l'Environnement (CEREGE) ; Institut de Recherche pour le Développement (IRD)-Institut National de la Recherche Agronomique (INRA)-Aix Marseille Université (AMU)-Collège de France (CdF (institution))-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS) | Spectropôle - Aix Marseille Université (AMU SPEC) ; Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)
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Afficher plus [+] Moins [-]anglais. Aging in water of a TiO2-based nanocomposite used in sunscreen cosmetics has been studied as a function of light and time. It consisted initially in a TiO2 core, coated with Al(OH)(3) and polydimethylsiloxane (PDMS) layers. Size measurement, coating alteration, and surface charge were followed by laser diffraction, TEM/EDS, ICP-AES and electrophoretic mobility measurement. The nanocomposite rapidly underwent progressive dispersion in the aqueous phase, enabled by the dissolution of the PDMS layer. A stable suspension of colloidal byproducts from 50 to 700 nm in size was formed. Their positively charged Al(OH)(3) surface was evidenced with an isoelectric point around 7-8, controlling the dispersion stability. The critical coagulation concentrations measured with NaCl and CaCl2 was 2 x 10(-2) and 8 x 10(-3) M respectively. The presence of natural organic matter affected the colloidal stability according to the NOM/byproduct ratio. A 2 wt% ratio favored bridging flocculation, whereas a 20 wt% ratio induced sterical stabilization. (C) 2010 Elsevier Ltd. All rights reserved.
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