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Modified Fenton's Reagent
Technology >
Modified Fenton's Reagent
ISOTECSM’s modified Fenton’s process is based on the
fundamental principles of Fenton’s chemistry. H.J.H. Fenton first
demonstrated the use of Fenton’s chemistry in 1894 by oxidation of
tartaric acid using a soluble iron-catalyzed decomposition of dilute
hydrogen peroxide under acidic conditions. The modified Fenton’s
process was developed with the fundamental goal of enhancing in
situ treatment of soil and groundwater contamination using
Fenton’s chemistry while mitigating the negatives associated with
application of Fenton’s reagent in its conventional form (such as
acidic pH, limited catalyst mobility, etc). The process generates
powerful free radicals when the catalyst reacts with hydrogen
peroxide. The principal chemical reaction associated with the modified
Fenton’s process is provided below.
H2O2 + Fe2+ => OH• + OH- +
Fe3+
Where,
H2O2 = Hydrogen Peroxide, Fe2+ =
Ferrous Ion, Fe3+ = Ferric Ion, OH• = Hydroxyl
Radicals
In addition to the initiation reaction (1) described above that
produces hydroxyl radical oxidants, the modified Fenton’s
process also produces superoxide radical and hydroperoxide anion
reductants by additional chain propagation reactions described
below. The perhydroxyl radical is known to be a weaker reductant
compared to superoxide radical and hydroperoxide anions.
H2O2 + OH• => HO2• + H2O
HO2• => H+ + O2•-
HO2• + O2•- => HO2-
+ O2
Where
O2•- = superoxide radical anion, HO2-
= hydroperoxide anion, HO2• = perhydroxyl radical
The
co-existing oxidation-reduction reactions associated with a modified
Fenton’s process promote enhanced desorption and degradation of
recalcitrant compounds. These include compounds such as carbon
tetrachloride and chloroform, which were previously considered
untreatable by Fenton’s chemistry
WHY USE MODIFIED
FENTON'S REAGENT?
ISOTEC's modified Fenton's Reagent is quickly emerging as the leading
remedial technique of the 21st century. However, if you are familiar
with how conventional Fenton's is most often applied, using strong
acids and high reagent concentrations under pressure, then you are
familiar with its shortcomings, often including incomplete treatment,
explosive reactions, organic vapor generation and contaminant
migration.
ISOTEC's modified Fenton's Reagent process was specifically designed
to overcome these problems. ISOTEC's patented catalysts allow reagents
at background neutral pH conditions to be effectively
distributed within the aquifer, destroying contaminants in saturated
soil and groundwater without generating organic vapors or high
temperatures.
COMPARISON OF
OTHER PEROXIDE-BASED TECHNOLOGIES
| Technology Features | Hydrogen Peroxide | Classic Fenton’s Reagent | Modified Fenton’s Reagent | | Aquifer Acidification | No | Yes |
No | | Hydroxyl Radical Production | Limited | Yes, if pH < 3 |
Yes | | Superoxide Radical Production | No | Limited |
Yes | | Controlled Reaction | No | No |
Yes | | Bioremediation Stimulation | Yes | Limited |
Yes |
The modified Fenton's Reagent process is an in-situ remedial treatment technology that destroys organic contamination through co-existing chemical oxidation and reduction. This process consists of injecting patented chelated iron catalysts and hydrogen peroxide into contaminated aquifers. As compared to conventional Fenton's Reagent, which require acidic conditions (pH~3), ISOTEC's modified Fenton's Reagent process is effective at neutral (pH~7) conditions. This is an important consideration in full-scale application, since acidifying an aquifer is typically impractical. Additionally, the production of superoxide, which is the driving reaction for contaminant reduction and desorption, is inhibited at acidic conditions. ISOTEC uses patented reagents designed for neutral subsurface conditions and efficient hydroxyl radical and superoxide generation. ISOTEC's oxidation and reduction method utilizes a site-specific delivery system designed to treat organic contaminants within an area of concern. ISOTEC oxidants and catalysts react with the organic contaminants within the subsurface producing innocuous by-products such as carbon dioxide and water (and chloride ions if chlorinated compounds are being treated).
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