Abstract

This work reviews an eco-friendly process for producing TiO2 via colloidal aqueous sol–gel synthesis, resulting in crystalline materials without a calcination step. Three types of colloidal aqueous TiO2 are reviewed: the as-synthesized type obtained directly after synthesis, without any specific treatment; the calcined, obtained after a subsequent calcination step; and the hydrothermal, obtained after a specific autoclave treatment. This eco-friendly process is based on the hydrolysis of a Ti precursor in excess of water, followed by the peptization of the precipitated TiO2. Compared to classical TiO2 synthesis, this method results in crystalline TiO2 nanoparticles without any thermal treatment and uses only small amounts of organic chemicals. Depending on the synthesis parameters, the three crystalline phases of TiO2 (anatase, brookite, and rutile) can be obtained. The morphology of the nanoparticles can also be tailored by the synthesis parameters. The most important parameter is the peptizing agent. Indeed, depending on its acidic or basic character and also on its amount, it can modulate the crystallinity and morphology of TiO2. Colloidal aqueous TiO2 photocatalysts are mainly being used in various photocatalytic reactions for organic pollutant degradation. The as-synthesized materials seem to have equivalent photocatalytic efficiency to the photocatalysts post-treated with thermal treatments and the commercial Evonik Aeroxide P25, which is produced by a high-temperature process. Indeed, as-prepared, the TiO2 photocatalysts present a high specific surface area and crystalline phases. Emerging applications are also referenced, such as elaborating catalysts for fuel cells, nanocomposite drug delivery systems, or the inkjet printing of microstructures. Only a few works have explored these new properties, giving a lot of potential avenues for studying this eco-friendly TiO2 synthesis method for innovative implementations.

Highlights

  • Photocatalysis is a well-established process for the effective and sustainable removal of a large range of organic pollutants, both in liquid and gaseous media [1]

  • The goal of this review is to evaluate the state of the art of the research into this not very well-known eco-friendly process for producing TiO2 via colloidal aqueous sol–gel synthesis, resulting inin crystalline materials without a calcination step

  • The aim of this review was to establish the state of the art of the research in the area of the little known eco-friendly process of producing TiO2 via colloidal aqueous sol–gel synthesis, resulting in a crystalline material without a calcination step

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Summary

Introduction

Photocatalysis is a well-established process for the effective and sustainable removal of a large range of organic pollutants, both in liquid and gaseous media [1] This phenomenon consists of a set of oxidation-reduction (redox) reactions between the organic compounds (pollutants) and the active species formed at the surface of an illuminated photocatalyst (usually a photoactivable semiconductor solid). Most works ergetic light be usedTiO for 2activation, corresponds to 5–8% of theasolar in will modifying materials which by doping or modification with largespectrum range of different [8] To prevent these limitations, several studies have been conducted [9,10,11,12]. Micelle [21],needed, hydrothermal [22],on and pyrolysis [23] These processes often use seSeveral processes exist to produce photocatalysts, the main methods being protocols.

Hydrolysis
Synthesis of TiO2 with in main
Crystallinity
As-Synthesized Aqueous TiO2
Acid Peptizing Agent
Basic Peptizing Agent
Aqueous TiO22after a Calcination Treatment
For temperatures belowfor
Calcination after Acidic Peptization
Evolution
Basic Peptization Followed by Calcination
Aqueous
Morphology of As-Synthesized Aqueous TiO2
Morphology of Aqueous TiO22 after Calcination Treatment
Morphology
Doping and Additives
Photocatalytic Properties
Photoactivity of As-Synthesized Aqueous TiO2
Photoactivity of Aqueous TiO2 after a Calcination Treatment
Photoactivity of Aqueous TiO2 after Hydrothermal Treatment
Addition Features for Aqueous Sol–Gel TiO2
Conclusions and Outlook
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