Cr(VI) has several industrial applications but it is one of the most dangerous pollutants because of its carcinogenicity and high toxicity. Thus, the removal of Cr(VI) by photocatalytic reduction was investigated. The catalyst applied, Ce–ZrO2, was immobilized, through a sol–gel process on a silicon carbide (SiC) support, to increase the efficiency and avoid using suspended nanoparticles. The influence of initial pH, humic acid (HA), and catalyst dosage was investigated for Cr(VI) containing solutions. Then, a real galvanizing industry effluent (Cr(VI) = 77 mg L-1mg.L−1, Zn = 1789 mg L−1) was treated. It was observed that Cr(VI) adsorption and photoreduction are greatly favored at low pH values. HA can decrease Cr(VI) adsorption but also acts as holes scavenger, reducing the electron–hole recombination, favoring then the photoreduction. With the immobilized Ce–ZrO2, more than 97% of Cr(VI) was removed from the diluted effluent. These results indicate the feasibility to treat Cr(VI) effluents even in the presence of other metals and natural organic matter. The developed material has great chemical and mechanical resistances and avoids the use of nanoparticles, dangerous for the environment and hard to recover. Moreover, solar light can be used to drive the process, which contributes to the development of more sustainable, cleaner, and cost-effective wastewater treatments.
1 December 2021 in Journal of Environmental Chemical Engineering
Natural water bodies and treated wastewaters contain an increasing variety of organic micropollutants with a negative impact on ecosystems and human health. Herein, we propose an integrated process based on membrane distillation and advanced oxidation, in which thermal energy is simultaneously used to drive the permeation of pure water through a hydrophobic membrane and to activate the generation of reactive oxygen species by a thermocatalytic perovskite, namely Ce-doped strontium ferrate. At a feed temperature of 65 °C, our thermocatalytic distillation apparatus can effectively retain and degrade bisphenol A, as model pollutant, while producing distilled water at the constant rate of 1.60 ± 0.03 L h−1 m−2, over four continuous runs. Moreover, the membrane makes degradation faster by concentrating the pollutant during filtration. Our technology is effective in the production of pure water without creating a toxic concentrate, it relies on simple process design, and it does not require high pressure or additional chemicals. In addition, it can potentially work continuously driven by renewable thermal energies or waste heat.