Related Experiment Video
Updated: Nov 19, 2025

Development and Validation of Chromium Getters for Solid Oxide Fuel Cell Power Systems
Published on: May 26, 2019
Hexavalent chromium reduction by gallic acid.
Christiana Mystrioti1, Stefania Koursari1, Anthimos Xenidis1
1Sch. of Mining and Metallurgical Eng., National Technical University of Athens, 15780, Greece.
Gallic acid effectively reduces toxic hexavalent chromium (Cr(VI)) to beneficial trivalent chromium (Cr(III)). This rapid reaction occurs under mild acidic conditions, offering a promising environmental cleanup solution.
Area of Science:
- Environmental Chemistry
- Green Chemistry
- Water Treatment Technologies
Background:
- Hexavalent chromium (Cr(VI)) is a toxic industrial pollutant released into the environment.
- Cr(VI) in wastewater poses significant environmental and health risks due to its toxicity and solubility.
- Trivalent chromium (Cr(III)) is an essential micronutrient, making Cr(VI) reduction a desirable remediation strategy.
Purpose of the Study:
- To investigate the reduction of hexavalent chromium (Cr(VI)) to trivalent chromium (Cr(III)) using gallic acid (GA).
- To evaluate the kinetics of Cr(VI) reduction by GA under varying pH, temperature, and Cr(VI) concentrations.
- To assess the efficiency of GA as a reducing agent for Cr(VI) remediation in contaminated waters.
Main Methods:
- Batch tests were conducted to study the reduction of Cr(VI) by gallic acid.
- The effects of pH (3-6), temperature (25-35 °C), and initial Cr(VI) concentration were systematically examined.
- Reaction kinetics were analyzed to determine the reaction order and rate under different conditions.
Main Results:
- Cr(VI) reduction by GA is a rapid process under mild acidic conditions (pH 3-5).
- The reduction follows a second-order kinetic with respect to Cr(VI) concentration in the pH range of 3-5.
- Complete reduction of 100 μM Cr(VI) was achieved in 20 min at pH 3 and 40 min at pH 4.
- At higher pH (5-6), the reduction mechanism changed, requiring significantly longer reaction times (10-42 hours).
- Slight acceleration of the reaction rate was observed with a temperature increase from 25 °C to 35 °C at pH 6.
Conclusions:
- Gallic acid is an effective natural reducing agent for the detoxification of Cr(VI) in contaminated water.
- Mild acidic conditions (pH 3-5) are optimal for rapid Cr(VI) reduction by gallic acid.
- The study demonstrates a promising, green chemistry approach for environmental remediation of Cr(VI) pollution.
Related Concept Videos
Acid Halides to Ketones: Gilman Reagent
As shown below, the mechanism proceeds in two steps. First, one of the alkyl groups of the reagent acts as a nucleophile and attacks the acyl carbon of the acid chloride to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen...
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Acid Halides to Alcohols: Grignard Reaction
Grignard reagents are a source of carbanions and function as nucleophiles. The mechanism begins with the nucleophilic attack by the carbanion at the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs,...
Redox Titration: Other Oxidizing and Reducing Agents
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...

