Photo-Fenton Degradation of Methyl Orange with Dunino Halloysite as a Source of Iron

The Fenton reaction is one of the most important processes for water and soil remediation, although this process has some drawbacks such as the use of H2O2 in large amounts, the formation of sludge due to the use of iron salts, and the need for acid pH values. Here we present the use of a natural clay, modified by acid treatment, as a heterogeneous catalyst to replace soluble iron salts and to avoid the use of water peroxide, resulting in a considerable increase in the attractiveness of the process. Halloysite (HT) clay from the Dunino mine consists of alumina and silica layers with the presence of iron species acting as a source of Fe ions. The etching of alumina layers using hydrochloric acid induces the release of iron species (mainly ions) in the solution, giving rise to the photodegradation activity of organic contaminants in water (i.e., Methyl Orange, MO) under UV irradiation without the need for hydrogen peroxide and avoiding the formation of sludges. MO adsorption properties and MO photodegradation ability were investigated for untreated and acid treated samples, respectively, to achieve the optimal process conditions. MO was not adsorbed on the clay's surface due to electrostatic repulsion, but a complete degradation was observed after three hours under UV irradiation. The kinetics of photodegradation and the values of the half-life time are presented as a measure of the degradation rate. The proposed process shows a new route for effective remediation of water containing biologically active organic substances dissolved in it.

Automated summary

The Fenton reaction plays a crucial role in water and soil remediation, but drawbacks such as the use of H2O2 and iron salts can be avoided by using acid-treated natural clay as a heterogeneous catalyst. This process effectively degrades organic contaminants in water under UV irradiation without the need for hydrogen peroxide, offering a new route for remediation of water contaminated with biologically active organic substances.