TiO2 photocatalysis and related surface phenomena

Jenny Schneider,*,† Masaya Matsuoka,‡ Masato Takeuchi,‡ Jinlong Zhang, Yu Horiuchi,‡ Masakazu Anpo,‡ and Detlef W. Bahnemann*,† †Institut fur Technische Chemie, Leibniz Universitaẗ Hannover, Callinstrasse 3, D-30167 Hannover, Germany ‡Faculty of Engineering, Osaka Prefecture University, 1 Gakuen-cho, Sakai Osaka 599-8531, Japan Key Lab for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, Shanghai 200237, China

Understanding TiO2 photocatalysis: mechanisms and materials.

http://publicationslist.org/data/meng.chong/ref-18/sdarticle.pdf

Recent Developments in Photocatalytic Water Treatment Technology: A Review

Photoinduced reactivity of titanium dioxide

Nano-sized TiO 2 photocatalytic water-splitting technology has great potential for low-cost, environmentally friendly solar-hydrogen production to support the future hydrogen economy. Presently, the solar-to-hydrogen energy conversion efficiency is too low for the technology to be economically sound. The main barriers are the rapid recombination of photo-generated electron/hole pairs as well as backward reaction and the poor activation of TiO 2 by visible light. In response to these deficiencies, many investigators have been conducting research with an emphasis on effective remediation methods. Some investigators studied the effects of addition of sacrificial reagents and carbonate salts to prohibit rapid recombination of electron/hole pairs and backward reactions. Other research focused on the enhancement of photocatalysis by modification of TiO 2 by means of metal loading, metal ion doping, dye sensitization, composite semiconductor, anion doping and metal ion-implantation. This paper aims to review the up-to-date development of the above-mentioned technologies applied to TiO 2 photocatalytic hydrogen production. Based on the studies reported in the literature, metal ion-implantation and dye sensitization are very effective methods to extend the activating spectrum to the visible range. Therefore, they play an important role in the development of efficient photocatalytic hydrogen production.

A review and recent developments in photocatalytic water-splitting using TiO2 for hydrogen production

Section 2: Arsenic in food

Lethal and sublethal effects of As(V) on early larval development of Rhinella arenarum and utility of AMPHITOX as an ecotoxicological test for As(V) solutions after treatment with zerovalent iron nanoparticles

As(Iii) Removal of Aqueous Solutions Using Zerovalent Iron Nanoparticles: The Role of the Uva-Vis Irradiation Wavelength

The photocatalytic and mechanical performance of TiO2 nanotubular coatings obtained by anodic oxidation of commercial titanium, using an NH4F and 3.5% v/v water in ethylene glycol solution as electrolyte was investigated. After the anodization, the coatings were thermally treated at 450 °C for 2 h. The effects of the anodizing voltage (40-80 V) and NH4F concentration (0.06, 0.15, 0.27 M) on the formation of the nanotube arrays were evaluated. Nanotube diameters (57 to 114 nm), wall thicknesses (4 to 13 nm), and lengths (5 to 17 µm) increased with the anodizing voltage and the NH4F concentration. The photocatalysts were characterized by scanning electron microscopy, glancing incidence X-ray diffraction, and UV-Vis diffuse reflectance spectroscopy. The mechanical properties of the photocatalysts were determined: adhesion using the tape test (ASTM D3359) and erosion resistance through a 3 h accelerated test. The photocatalytic activity of the nanotubes under UV irradiation was evaluated using hexavalent chromium (Cr(VI)) in the presence of ethylenediaminetetraacetic acid (EDTA), using a 1.25 EDTA/Cr(VI) molar ratio solution at pH 2. A complete Cr(VI) transformation after 3 h of irradiation was obtained for all samples, with a better performance than that of an immobilized P25 sample. The photocatalyst obtained with 0.27 M NH4F at 40 V presented a good behavior in adherence and erosion resistance, together with a very good photocatalytic activity. This novel analysis, combining photocatalytic and mechanical tests, proved that the new TiO2 nanotubular coatings could be successfully used as immobilized photocatalysts in photoreactors for water treatment. 

https://link.springer.com/content/pdf/10.1007/s43630-022-00257-5.pdf

Photocatalytic and mechanical properties of immobilized nanotubular TiO_2 photocatalysts obtained by anodic oxidation: a novel combined analysis

The plasma electrolytic oxidation (PEO) is a variation of the anodic oxidation technique, one of the simplest and most economical methods to obtain crystalline and porous TiO2 coatings. Beyond the conventional approach of establishing a relationship between the variables of synthesis and the characteristics of the TiO2 coatings, a new figure of merit was defined in the present work for the synthesis of TiO2 coatings by PEO: the total energy per unit of surface (TSE). A strong relationship was found between TSE and the TiO2 anatase fraction. The application of TSE, together with the known influence of the variables of synthesis on the coating characteristics, allows a prediction, previously to the anodization and with reasonable precision, of the anatase fraction and the pore diameter of the coating. Applying the TSE new concept, three coatings were successfully designed. This is the first step toward a surface design using the PEO technique. 

Marta I. Litter

Papers

Section 2: Arsenic in food

Lethal and sublethal effects of As(V) on early larval development of Rhinella arenarum and utility of AMPHITOX as an ecotoxicological test for As(V) solutions after treatment with zerovalent iron nanoparticles

As(Iii) Removal of Aqueous Solutions Using Zerovalent Iron Nanoparticles: The Role of the Uva-Vis Irradiation Wavelength

Photocatalytic and mechanical properties of immobilized nanotubular TiO_2 photocatalysts obtained by anodic oxidation: a novel combined analysis

Total Specific Energy as a New Figure of Merit for the Design of Porous TiO2 Surfaces Synthesized via Plasma Electrolytic Oxidation