H2O2/periodate: a novel advanced oxidation process.

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International audienceIn recent years, heterogeneous photocatalysis has emerged as a new effective, powerful, clean, and safe decontamination technology for the treatment of organic pollutants and the transformation of hazardous chemicals into different forms. This review focuses on the recent development of various conventional technologies of reactors designated for the photodegradation of hazardous organic pollutants with their limitations. This phenomenon is strongly influenced by reaction conditions such as temperature of reaction, pH, light intensity and wavelength, pollutant concentration, photocatalyst quantity, relative humidity (RH), and other parameters. The catalyst photoactivity depends on the structural characteristics of the semiconductor, its morphology, and its particles size. This paper presents the progression of photocatalytic reactors for synthetic dyes degradation with special consideration to the use of supported photocatalyst and nanostructured titanium supported over volcanic ashes, owing to the major advantage of an easy separation of the catalyst when compared to homogenous system, namely suspended catalyst. In addition, special attention was paid to the literature dealing with the promotion of light efficiency by testing various light sources. © 2016, Copyright © Taylor & Francis Group, LLC

We have recently reported that the reaction of H2O2/IO4− could be a new advanced oxidation process for water treatment [N. E. Chadi, S. Merouani, O. Hamdaoui, M. Bouhelassa and M. Ashokkumar, Environ. Sci.: Water Res. Technol., 2019, 5, 1113–1123].

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In this work, we have explored for the first time the potential application of trace‐Fe(III)/chlorine system as an innovative oxidation technology for the degradation of persistent textile dyes. Fe(III)/chlorine combination improved the dye removal by ~40% within 30 s, as compared with chlorination alone, mainly through a radical pathway induced by the catalytic activation of chlorine in the presence of Fe(III). A chemical probe method was used for identifying the main reactive species. Cl2●− was found to be the key species responsible of huge abatement of dyes in the Fe(III)/chlorine system, whereas ●OH and Cl● can participate with only ~5% in the overall removal efficiency. At pH 3, 77% of reactive green 12 (RG12) was removed after 30 s, and then the removal efficiency diminished to 60% at pH 4, 20% at pH 5, and ~10% at pH 6 and 7. However, the best implication of free radicals was achieved at pH 4, at which the degradation rate was 3.3 time higher than that of chlorination alone. The dye removal efficiency increased with an increase in chlorine and iron loads up to certain optimums, but detrimental effect was observed at higher dosage levels. An increase in the solution temperature notably accelerated the removal yield (i.e., 81% of RG12 was removed at 50°C against 67% at 30°C and 57% at 10°C). NO2− and HSO3− as well as the cationic surfactant Adogen 464 showed strongest inhibiting effect on the performance of the process. Based on these findings, the Fe(III)/chlorine process is highly efficient in removing dyes from wastewaters.

The aim of our research is to apply experimental design methodology to the optimization of photocatalytic degradation of indole present in wastewater. Heterogeneous photocatalysis for the oxidation of organic biorecalcitrant pollutants in water is an environmental promising method. We used the response surface methodology (RSM) for the modelization and optimization of the photodegradation of indole in the presence of titanium dioxide. The effect of indole concentration, UV intensity and stirring speed on the yield of indole degradation was determined. According to the mathematic optimization of the process, the optimum point when 100% of degradation is achieved is given by the following values: UV intensity = 250 W/m 2 , stirring speed = 536.36 tr/min and initial indole concentration = 10.10 mg/l.