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Related Concept Videos

Redox Reactions01:24

Redox Reactions

Oxidation-reduction or redox reactions involve the transfer of electrons from one molecule or atom to another. When an atom gains an electron, another atom must lose an electron, meaning oxidation and reduction must occur together. Since the redox occurs in pairs, the atom that gets oxidized is also called the reducing agent or reductant, and the atom that is reduced is also called the oxidizing agent or oxidant. A straightforward way to remember the definitions of oxidation and reduction is...
Redox Reactions01:27

Redox Reactions

Redox reactions are vital biochemical processes that underpin energy metabolism in cells. These reactions involve the transfer of electrons between molecules, occurring in tandem as oxidation and reduction. Oxidation refers to the loss of electrons, while reduction denotes their gain. This coupling ensures the seamless flow of electrons through metabolic pathways. For example, in bacterial metabolism, glucose undergoes oxidation to carbon dioxide, while oxygen is simultaneously reduced to...
Acid Mine Drainage01:19

Acid Mine Drainage

Mining activities that disturb sulfide-rich rocks, particularly those containing pyrite (FeS₂), initiate a cascade of geochemical and microbiological processes with serious environmental implications. When exposed to air and water, pyrite undergoes oxidation, releasing sulfate, ultimately forming sulfuric acid and mobilizing heavy metals into surrounding water systems. This phenomenon, known as acid mine drainage (AMD), results in low pH waters laden with toxic elements that threaten aquatic...
Redox Titration: Other Oxidizing and Reducing Agents01:26

Redox Titration: Other Oxidizing and Reducing Agents

Besides iodine, other oxidizing or reducing agents can serve as titrants in redox titrations. Common oxidizing titrants include KMnO4, cerium(IV), and K2Cr2O7. The choice of oxidizing titrants depends on factors like stability, cost, analyte strength, and reaction rate between the analyte and titrant. KMnO4 is a strong oxidizing titrant that reduces from Mn(VII) to Mn(II) in a highly acidic solution, simultaneously oxidizing the analyte to a higher oxidation state. In this case, KMnO4 acts as a...
Redox Equilibria: Overview01:23

Redox Equilibria: Overview

A reduction-oxidation reaction is commonly called a redox reaction. In a redox reaction, electrons are transferred from one species to another rather than being shared between or among atoms. The reducing agent or reductant is the species that loses electrons and gets oxidized in the process. The species that gains electrons and gets reduced in the process is the oxidizing agent or oxidant. Redox reactions are represented as two separate equations called half-reactions, where one equation...
Ladder Diagrams: Redox Equilibria01:30

Ladder Diagrams: Redox Equilibria

Ladder diagrams are useful tools for understanding redox equilibrium reactions, especially the effects of concentration changes on the electrochemical potential of the reaction. The vertical axis in the redox ladder diagrams represents the electrochemical potential, E. The area of predominance is demarcated using the Nernst equation.
Consider the Fe3+/Fe2+ half-reaction, which has a standard-state potential of +0.771 V. At potentials more positive than +0.771 V, Fe3+ predominates, whereas Fe2+...

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Related Experiment Video

Updated: May 15, 2026

Experimental Column Setup for Studying Anaerobic Biogeochemical Interactions Between Iron (Oxy)Hydroxides, Trace Elements, and Bacteria
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Arsenic release from deep natural solid matrices under experimentally controlled redox conditions.

A Molinari1, L Guadagnini, M Marcaccio

  • 1Politecnico di Milano, DIIAR, Piazza L. Da Vinci 32, 20133 Milano, Italy. ant.molinari2002@libero.it

The Science of the Total Environment
|January 1, 2013
PubMed
Summary

Iron (Fe) and redox changes significantly impact arsenic (As) release from soil, particularly in vegetal matter. These findings explain critical arsenic levels in Emilia-Romagna aquifers.

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Last Updated: May 15, 2026

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Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

Area of Science:

  • Environmental Science
  • Geochemistry
  • Hydrogeology

Background:

  • Arsenic (As) contamination in groundwater is a global environmental concern.
  • Aquifer systems can act as reservoirs for naturally occurring arsenic.
  • Iron (Fe) cycling is known to influence arsenic mobility in soils and sediments.

Purpose of the Study:

  • To investigate the role of iron (Fe) in arsenic (As) release from different soil matrices under varying redox conditions.
  • To correlate arsenic mobilization with iron release and redox potential in natural soil samples.
  • To explain the high arsenic concentrations observed in Emilia-Romagna aquifers.

Main Methods:

  • Batch experiments were conducted on two distinct soil samples (sand and vegetal matter) from an Italian aquifer.
  • Alternating aerobic and anaerobic conditions were applied, mimicking field redox and pH variations.
  • Arsenic and iron concentrations were measured in relation to oxidation-reduction potential.

Main Results:

  • Arsenic mobilization was strongly correlated with abrupt changes in redox conditions for both soil types.
  • Vegetal matter exhibited high arsenic binding capacity and significant arsenic release.
  • Arsenic release was directly linked to the release of iron from the soil matrices.

Conclusions:

  • The study confirms that fluctuating redox conditions are a primary driver of arsenic release from soils.
  • High natural arsenic content in vegetal matter, combined with redox oscillations, likely contributes to critical arsenic levels in Emilia-Romagna aquifers.
  • Iron mobilization plays a crucial role in the release mechanism of arsenic from these soil environments.