Английская Википедия:Fenton's reagent

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Шаблон:Short description Fenton's reagent is a solution of hydrogen peroxide (H₂O₂) and an iron catalyst (typically iron(II) sulfate, FeSO₄). It is used to oxidize contaminants or waste water as part of an advanced oxidation process. Fenton's reagent can be used to destroy organic compounds such as trichloroethylene and tetrachloroethylene (perchloroethylene). It was developed in the 1890s by Henry John Horstman Fenton as an analytical reagent.

Overview

Iron(II) is oxidized by hydrogen peroxide to iron(III), forming a hydroxyl radical and a hydroxide ion in the process. Iron(III) is then reduced back to iron(II) by another molecule of hydrogen peroxide, forming a hydroperoxyl radical and a proton. The net effect is a disproportionation of hydrogen peroxide to create two different oxygen-radical species, with water (H⁺ + OH⁻) as a byproduct.

The free radicals generated by this process then engage in secondary reactions. For example, the hydroxyl is a powerful, non-selective oxidant. Oxidation of an organic compound by Fenton's reagent is rapid and exothermic and results in the oxidation of contaminants to primarily carbon dioxide and water.

Reaction (Шаблон:EquationNote) was suggested by Haber and Weiss in the 1930s as part of what would become the Haber–Weiss reaction.

Iron(II) sulfate is typically used as the iron catalyst. The exact mechanisms of the redox cycle are uncertain, and non-OH^• oxidizing mechanisms of organic compounds have also been suggested.Шаблон:Citation needed Therefore, it may be appropriate to broadly discuss Fenton chemistry rather than a specific Fenton reaction.

In the electro-Fenton process, hydrogen peroxide is produced in situ from the electrochemical reduction of oxygen.

Fenton's reagent is also used in organic synthesis for the hydroxylation of arenes in a radical substitution reaction such as the classical conversion of benzene into phenol.

An example hydroxylation reaction involves the oxidation of barbituric acid to alloxane. Another application of the reagent in organic synthesis is in coupling reactions of alkanes. As an example tert-butanol is dimerized with Fenton's reagent and sulfuric acid to 2,5-dimethyl-2,5-hexanediol. Fenton's reagent is also widely used in the field of environmental science for water purification and soil remediation. Various hazardous wastewater were reported to be effectively degraded through Fenton's reagent.

Effect of pH on formation of free radicals

pH affects the reaction rate due to a variety of reasons. At a low pH, complexation of Шаблон:Chem2 also occurs, leading to lower availability of Шаблон:Chem2 to form reactive oxidative species (OH^•). Lower pH also results in the scavenging of ^•OH by excess Шаблон:Chem2, hence reducing its reaction rate. Whereas at high pH, the reaction slows down due to precipitation of Fe(OH)₃, lowering the concentration of the Шаблон:Chem2 species in solution. Solubility of iron species is directly governed by the solution's pH. Шаблон:Chem2 is about 100 times less soluble than Шаблон:Chem2 in natural water at near-neutral pH, the ferric ion concentration is the limiting factor for the reaction rate. Under high pH conditions, the stability of the H₂O₂ is also affected, resulting in its self-decomposition. Higher pH also decreased the redox potential of ^•OH thereby reducing its effectiveness. pH plays a crucial role in the formation of free radicals and hence the reaction performance. Thus ongoing research has been done to optimize pH and amongst other parameters for greater reaction rates.

Impacts of operation pH on reaction rate

Low pH	Formation of [Fe(H2O)6]2+ complex, hence reducing Fe2+ for radical generation
	Scavenging of •OH by excess H+
High pH	Lower redox potential of •OH
	Self-decomposition of H2O2 due to decreased stability at high pH
	Precipitation of Fe(OH)3 species in solution

Biomedical implications

The Fenton reaction has different implications in biology because it involves the formation of free radicals by chemical species naturally present in the cell under in vivo conditions. Transition-metal ions such as iron and copper can donate or accept free electrons via intracellular reactions and so contribute to the formation, or at the contrary to the scavenging, of free radicals. Superoxide ions and transition metals act in a synergistic way in the appearance of free radical damages. Therefore, although the clinical significance is still unclear, it is one of the viable reasons to avoid iron supplementation in patients with active infections, whereas other reasons include iron-mediated infections.

Applications

Шаблон:See also Fenton's reagent is used as a sewage treatment agent.

Fenton's reagent can be used in different chemical procesess that supply hydroxyl ion or oxidize certain compounds:

• The first stage of Fenton’s reaction (oxidation of Fe³⁺ with hydrogen peroxide) is used in Haber–Weiss reaction
• Fenton's reagent can be used in organic synthesis reactions: e.g. hydroxylation of arenes via a free radical substitution
• Conversion of benzene into phenol by using Fenton's reagent
• Oxidation of barbituric acid into alloxan.
• Coupling reactions of alkanes

Fenton-like reagent

Mixtures of Шаблон:Chem2 and Шаблон:Chem2 are called Fenton reagent. If Шаблон:Chem2 is replaced by Шаблон:Chem2, it is called Fenton-like reagent.

Numerous transition metal ions and their complexes in their lower oxidation states (Шаблон:Chem2) were found to have the oxidative features of the Fenton reagent, and, therefore, the mixtures of these metal compounds with Шаблон:Chem2 were named "Fenton-like" reagents.

See also

• Carbon monoxide-releasing molecules

Further reading

• Шаблон:Cite journal
• Шаблон:Cite journal

External links

• Reference Library Peroxide Applications
• Companies that use Fenton's Reagent for chemical remediation: ORIN