A tubular ceramic membrane coated with TiO2-P25 for radial addition of H2O2 towards AMX removal from synthetic solutions and secondary urban wastewater.

This work aims to integrate several hydrogen peroxide (H2O2) activation mechanisms, photolysis (UVC irradiation), chemical electron transfer (TiO2-P25 photocatalysis), and reaction with TiO2-P25 in dark conditions, for reactive oxygen species (ROS) generation towards the removal of contaminants of emerging concern (CECs), in a single unit operated in continuous-flow mode. An H2O2 stock solution is fed by the lumen side of a tubular ceramic membrane, delivering the oxidant to the (i) catalyst immobilized in the membrane shell-side and (ii) annular reaction zone (ARZ, space between membrane shell-side and outer quartz tube) where CECs contaminated water flows with a helix trajectory, being activated by UV light provided by four lamps placed symmetrically around the reactor. First, the effect of several parameters in the removal of a CEC target molecule, amoxicillin (AMX), was evaluated using a synthetic solution ([AMX]inlet = 2.0 mg L-1): (i) light source (UVA or UVC radiation), (ii) H2O2 dose, (iii) H2O2 injection method (radial permeation vs. upstream injection), and (iv) number of TiO2-P25 layers deposited on the membrane. The UVC/H2O2/TiO2 system with radial addition of H2O2 (20 mg L-1) and 9-TiO2-P25 layers provided the highest AMX removal efficiency (72.2 ± 0.5%) with a UV fluence of 45 mJ cm-2 (residence time of 4.6 s), due to the synergic effect of four mechanisms: (i) AMX photolysis, (ii) H2O2 photocleavage, (iii) TiO2-P25 photoactivation, and (iv) chemical reactions between H2O2 and TiO2-P25. The urban wastewater matrix showed a negative effect on AMX removal (~44%) due to the presence of ROS scavengers and light-filtering species.

Engineering and modeling perspectives on photocatalytic reactors for water treatment.

The debate on whether photocatalysis can reach full maturity at commercial level as an effective and economical process for treatment and purification of water and wastewater has recently intensified. Despite a bloom of scientific investigations in the last 30 years, particularly with regards to innovative photocatalytic materials, photocatalysis has so far seen a few industrial applications. Regardless of the points of view, it has been realized that research on reactor design and modeling are now equally urgent to match the extensive research carried out on innovative photocatalytic materials. In reality, the development of photocatalytic reactors has advanced steadily in terms of modeling and reactor design over the last two decades, though this topic has captured a smaller specialized audience. In this critical review, we introduce the latest developments on photocatalytic reactors for water treatment from an engineering perspective. The focus is on the modeling and design of photocatalytic reactors for water treatment at pilot- or at greater scale. Photocatalytic reactors utilizing both natural sunlight and UV irradiation sources are comprehensively discussed. The most promising photoreactor designs and models are examined giving key design guidelines. Other engineering considerations, such as operation, cost analysis, patents, and several industrial applications of photocatalytic reactors for water treatment are also presented. The dissemination of key photocatalytic reactor design principles among the scientific community and the water industry is currently one of the greatest obstacles in translating PWT research into widespread real-world application.

Synthesis of Mg-Al layered double hydroxides by electrocoagulation.

Recently, layered double hydroxides (LDHs) have attracted much consideration due to their versatility and easily manipulating properties and their potential applications such as anion exchangers, support of catalysts, flame retardants, biomedical drug delivery. A novel method for the in-situ preparation in situ of LDHs, using electrocoagulation (EC) processes was developed, the EC process was performed under two different conditions, at 5 mA m-2, changing polarity of the electrodes to find out the composition that leads to LDHs generation. The final product was characterized using XRD, BET and FTIR techniques. This method presented the following advantages: (1) Simultaneously LDHs synthesis and wastewater treatment by ion removal; (2) Polarity control allows to manipulate the M2+/M3+ molar ratio, LDHs properties and its potential applications; (3) The method spent less time to carry out the synthesis and; (4) it did not need complicated solid-liquid separation processes.