Javier Marugán

Removal of cyanides in wastewater by supported TiO2-based photocatalysts

Abstract Titania supported samples on different types of silica have been prepared through a sol–gel method followed by hydrothermal processing. The photocatalytic activity of the samples was tested for free cyanides photo-oxidation. As compared to commercial TiO2 all the synthesised materials showed not only similar photocatalytic efficiencies but improved recovery properties. The degradation of iron(III) cyanocomplexes was also studied in the absence or presence of titania catalyst. In all cases, a photoinduced CN− released from the complex takes place through a homogeneous process. The further oxidation of those cyanides ions to cyanate species is significantly enhanced in the presence of the catalyst in which mesostructured SBA-15 silica is used as support.

Analogies and differences between photocatalytic oxidation of chemicals and photocatalytic inactivation of microorganisms

This study reports the analogies and differences found when comparing TiO(2) photocatalytic treatment for chemical oxidation and microorganisms inactivation, using methylene blue and Escherichia coli as references, respectively. In both processes the activation is based on the same physicochemical phenomena and consequently a good correlation between them is observed when analyzing the effect of operational variables such as catalyst concentration or incident radiation flux, both factors influencing common stages such radiation absorption and generation of reactive oxygen species. However, different microbiological aspects (osmotic stress, repairing mechanism, regrowth, bacterial adhesion to the titania surface, etc) makes disinfection kinetics significantly more complex than the first-order profiles usually observed for the oxidation of chemical pollutants. Moreover, bacterial inactivation reactions are found to be extremely sensitive to the composition of water and modifications of the catalysts in comparison with the decolorization of the dye solutions, showing opposite behaviors to the presence of chlorides, incorporation of silver to the catalysts or the use of different types of immobilized TiO(2) systems. Therefore, the activity observed for the photocatalytic oxidation of organics can not be always extrapolated to photocatalytic disinfection processes.

Emerging micropollutant oxidation during disinfection processes using UV-C, UV-C/H2O2, UV-A/TiO2 and UV-A/TiO2/H2O2.

Regeneration of wastewater treatment plant effluents constitutes a solution to increase the availability of water resources in arid regions. Water reuse legislation imposes an exhaustive control of the microbiological quality of water in the operation of disinfection tertiary treatments. Additionally, recent reports have paid increasing attention to emerging micropollutants with potential biological effects even at trace level concentration. This work focuses on the evaluation of several photochemical technologies as disinfection processes with the aim of simultaneously achieving bacterial inactivation and oxidation of pharmaceuticals as examples of emerging micropollutants typically present in water and widely studied in the literature. UV-C-based processes show a high efficiency to inactivate bacteria. However, the bacterial damages are reversible and only when using H(2)O(2), bacterial reproduction is affected. Moreover, a complete elimination of pharmaceutical compounds was not achieved at the end of the inactivation process. In contrast, UV-A/TiO(2) required a longer irradiation time to inactivate bacteria but pharmaceuticals were completely removed along the process. In addition, its oxidation mechanism, based on hydroxyl radicals (OH), leads to irreversible bacterial damages, not requiring of chemicals to avoid bacterial regrowth. For UV-A/TiO(2)/H(2)O(2) process, the addition of H(2)O(2) improved Escherichia coli inactivation since the cell wall weakening, due to OH attacks, allowed H(2)O(2) to diffuse into the bacteria. However, a total elimination of the pharmaceuticals was not achieved during the inactivation process.

Comparative evaluation of acute toxicity by Vibrio fischeri and fern spore based bioassays in the follow- up of toxic chemicals degradation by photocatalysis

The development of efficient bioassays is a necessary step for cost-effective environmental monitoring and evaluation of novel decontamination technologies. Marine Vibrio fischeri kits have demonstrated to be extremely sensitive but lack of ecological relevance, especially when assessing impacts on freshwater higher organisms. A novel riparian are fern spore microbioassay could merge higher ecological relevance and reduced costs. The aim of this work is the comparative evaluation of the V. fischeri and fern spore bioassays for the follow up of detoxification processes of water contaminated with cyanide and phenol by advanced oxidation technologies, using heterogeneous photocatalysis as example. In both cases, EC(50) values differed significantly for V. fischeri commercial kit, V. fischeri lab cultures and Polystichum setiferum fern spores (1.9, 16 and 101 mg cyanide L(-1) and 27.0, 49.3 and 1440 mg phenol L(-1), respectively). Whereas V. fischeri bioassays are extremely sensitive and dilution series must be prepared, toxicant solutions can be directly applied to spores. Spore microbioassay was also useful in the follow up of photoxidation processes of cyanide and phenol, also reflecting the formation of intermediate degradation by-products even more toxic than phenol. We conclude that this new microbioassay is a promising cost-effective tool for the follow up of decontamination processes.

Solar photocatalytic disinfection with immobilised TiO2 at pilot-plant scale

The photocatalytic disinfection efficiency has been investigated for two immobilized TiO(2) catalytic systems (wall reactor and fixed-bed reactor) in a solar pilot plant. Their performances have been compared with the use of a slurry reactor and the solar disinfection without catalyst. The use of photocatalytic TiO(2) wall reactors does no show clear benefits over the solar disinfection process in the absence of catalyst. The reason is that the efficiency of the solar disinfection is so high that the presence of titania in the reactor wall reduces the global efficiency due to the competition for the absorption of photons. As expected, the maximum efficiency was shown by the slurry TiO(2) reactor, due to the optimum contact between bacteria and catalyst. However, it is noticeable that the use of the fixed-bed reactor leads to inactivation rate quite close to that of the slurry, requiring comparable accumulated solar energy of about 6 kJ L(-1) to achieve a 6-log decrease in the concentration of viable bacteria and allowing a total disinfection of the water (below the detection limit of 1 CFU mL(-1)). Not only the high titania surface area of this configuration is responsible for the bacteria inactivation but the important contribution of the mechanical stress has to be considered. The main advantage of the fixed-bed TiO(2) catalyst is the outstanding stability, without deactivation effects after ten reaction cycles, being readily applicable for continuous water treatment systems.

Simultaneous photocatalytic oxidation of pharmaceuticals and inactivation of Escherichia coli in wastewater treatment plant effluents with suspended and immobilised TiO(2).

Simultaneous Escherichia coli inactivation and oxidation of pharmaceuticals in simulated wastewater treatment plant effluents has been investigated using a photocatalytic treatment with TiO(2) in suspension and immobilised onto a fixed-bed reactor. Non-photocatalytic reference experiments of dark adsorption and photolysis showed a higher sensitivity of E. coli towards the chemical composition of water in comparison with the concentration of pharmaceuticals that remains unaffected. Moreover, it must be underlined that the presence of pharmaceuticals (including antibiotics) did not seem to affect the bacterial viability at such low concentrations. Concerning photocatalytic experiments, both suspended and immobilised TiO(2) were able to simultaneously inactivate and oxidise both kinds of pollutants (bacteria and pharmaceuticals). The fixed-bed reactor showed similar activity to that of the slurry without deactivation after several cycles of reuse. That makes TiO(2) photocatalysis a quite interesting technology for the treatment of drinking water supplies or wastewater plant effluents, allowing the removal of emerging contaminants such as pharmaceuticals during the disinfection treatment.

Kinetics and influence of water composition on photocatalytic disinfection and photocatalytic oxidation of pollutants.

This work is focused on the comparison between the photocatalytic inactivation of Escherichia coli and the photocatalytic oxidation of methylene blue, regarding the reaction kinetics and the influence of water composition. Disinfection profiles show an initial delay, in contrast with the exponential decay shown by the decolorization of methylene blue solutions. A serial‐event mechanism is proposed for both disinfection and mineralization processes, the number of intermediate species being the main difference between them. Concerning the influence of water composition, inactivation of bacteria is more sensitive to the presence of inorganic ions and/or organic matter in the solution. In some cases opposite behaviours are observed, such as in the presence of chloride ions, which enhance the disinfection rate but decrease degradation activity for methylene blue. Consequently, the results obtained in the evaluation of photocatalytic processes for the degradation of chemical pollutants cannot be always extrapolated to the inactivation of microorganisms.

Photocatalytic gold recovery from spent cyanide plating bath solutions

A new procedure is presented for the photocatalytic treatment of the highly stable gold-cyanide complexes remaining in spent plating bath solutions. The process allows the recovery of gold by photocatalytic reduction, increasing simultaneously the availability of cyanide for removal treatment. Gold recovery requires a non-oxidant atmosphere and the presence of hydroxyl radical scavengers. The use of mixed TiO2/SiO2 photocatalysts leads to an improvement in the gold recovery rate.

Photocatalytic inactivation of E. faecalis in secondary wastewater plant effluents

Photocatalytic inactivation of Enterococcus faecalis using TiO(2) suspensions was investigated and compared to the inactivation of the most commonly used faecal indicator strain Escherichia coli. In contrast to the inactivation in pure deionized water, disinfection of effluents from the biological process of an urban wastewater plant showed a longer initial lag phase and higher survival fractions after several hours of irradiation. Moreover, the fluctuation of the composition of the effluents strongly affects the overall inactivation rate, not directly related to changes in the values of organic matter content. Additionally, it was found that E. faecalis seems to be more resistant than E.coli towards the photocatalytic treatment. These results could be related to the differences in the cell wall structure of both microorganisms. The main conclusion of this work is that attention must be paid when transferring results obtained for model organism to real bacteria consortia and from laboratory experiments with deionized water to effluents from sewage plants.

Electrochemical Enhancement of Photocatalytic Disinfection on Aligned TiO2 and Nitrogen Doped TiO2 Nanotubes

TiO2 photocatalysis is considered as an alternative to conventional disinfection processes for the inactivation of waterborne microorganisms. The efficiency of photocatalysis is limited by charge carrier recombination rates. When the photocatalyst is immobilized on an electrically conducting support, one may assist charge separation by the application of an external electrical bias. The aim of this work was to study electrochemically assisted photocatalysis with nitrogen doped titania photoanodes under visible and UV-visible irradiation for the inactivation of Escherichia coli. Aligned TiO2 nanotubes were synthesized (TiO2-NT) by anodizing Ti foil. Nanoparticulate titania films were made on Ti foil by electrophoretic coating (P25 TiO2). N-doped titania nanotubes and N,F co-doped titania films were also prepared with the aim of extending the active spectrum into the visible. Electrochemically assisted photocatalysis gave higher disinfection efficiency in comparison to photocatalysis (electrode at open circuit) for all materials tested. It is proposed that electrostatic attraction of negatively charged bacteria to the positively biased photoanodes leads to the enhancement observed. The N-doped TiO2 nanotube electrode gave the most efficient electrochemically assisted photocatalytic inactivation of bacteria under UV-Vis irradiation but no inactivation of bacteria was observed under visible only irradiation. The visible light photocurrent was only a fraction (2%) of the UV response.