Volume 217, Issue 20 pp. 2321-2329
Full Paper

Colloidal and Supported TiO2: Toward Nonextractable and Recyclable Photocatalysts for Radical Polymerizations in Aqueous Dispersed Media

Emeline Lobry

Emeline Lobry

Laboratory of Macromolecular Photochemistry and Engineering, University of Haute-Alsace, 3 rue Alfred Werner, 68093 Mulhouse Cedex, France

Search for more papers by this author
Abdoul Salam BT Bah

Abdoul Salam BT Bah

Laboratory of Macromolecular Photochemistry and Engineering, University of Haute-Alsace, 3 rue Alfred Werner, 68093 Mulhouse Cedex, France

Search for more papers by this author
Loïc Vidal

Loïc Vidal

Institut de Science des Matériaux de Mulhouse, CNRS UMR 7361, University of Haute-Alsace, 15 rue Jean Starcky, 68057 Mulhouse, France

Search for more papers by this author
Esther Oliveros

Esther Oliveros

Laboratoire des Interactions Moléculaires et Réactivité Chimique et Photochimique (IMRCP), UMR 5623-CNRS/UPS, Université Toulouse III Paul Sabatier, 118, route de Narbonne, 31062 Toulouse Cedex 9, France

Search for more papers by this author
André M. Braun

André M. Braun

Engler-Bunte-Institute, Karlsruhe Institute of Technology, 76131 Karlsruhe, Germany

Search for more papers by this author
Adrien Criqui

Adrien Criqui

Mäder Research, MADER GROUP, 130 rue de la Mer Rouge, 68200 Mulhouse, France

Search for more papers by this author
Abraham Chemtob

Corresponding Author

Abraham Chemtob

Institut de Science des Matériaux de Mulhouse, CNRS UMR 7361, University of Haute-Alsace, 15 rue Jean Starcky, 68057 Mulhouse, France

E-mail: [email protected]Search for more papers by this author
First published: 20 July 2016
Citations: 18

Abstract

Two high surface area titania forms, dispersed as stable nanoparticles or coated on fused silica microfiber, are used as nonleachable photocatalysts for the radical photopolymerization of methyl methacrylate miniemulsion in water. At low loading (0.17 wt%/wtmonomer), both nanoscale TiO2 yield ≈50% conversion after 10 min UV irradiation, compared to 63% with a conventional type I photoinitiatior (hydroxyacetophenone). High-molecular-weight values (>180 kDa) and a polydispersity index of about 1.5 are achieved, indicating that undesirable degradation is negligible. In the proposed mechanism, a surface initiation takes place through the generation of hydroxyl radicals from H2O oxidation. It is shown that irradiance and TiO2 content are two key parameters for controlling molecular weight and conversion values. The supported TiO2 form can be easily recovered and reused up to four times, despite a gradual reduction in conversion. Deposited on the wall of the annular photochemical reactor, it enables reaction scaling-up.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.