Related Experiment Video
Updated: Mar 3, 2026

Experimental Column Setup for Studying Anaerobic Biogeochemical Interactions Between Iron OxyHydroxides, Trace Elements, and Bacteria
Published on: December 19, 2017
An insight into mercury reduction process by humic substances in aqueous medium under dark condition
Krushna Vudamala1, Parthasarathi Chakraborty2, Budati Bala Venkata Sailaja3
1CSIR-National Institute of Oceanography, Dona Paula, Goa, 403004, India.
Abstract:
Mercury (Hg) reduction by humic substances (HS) in the aquatic medium under the dark condition is a poorly understood but important process in Hg biogeochemical cycling. In this study, an effort was made to provide a better understanding of Hg(II) reduction by well-characterized humic substances under dark condition. Reduction of Hg(II) by dissolved HS in aquatic systems increases with increasing Hg loading. However, Hg(II) reduction gradually decreases with the increasing total S content and oxygen containing functional groups in the dissolved HS under dark condition. Increasing major cation concentration decreases the rate of Hg(II) reduction in aquatic systems. High concentration of Ca2+ ion slows down the intermolecular electron transfer from HS to Hg(II) and inhibits the formation of Hg0 in absence of light. This study indicates that complexation of Hg(II) and HS is essential for Hg reduction under dark condition.
Related Concept Videos
Oxymercuration-Reduction of Alkenes
Extraction: Advanced Methods
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...
Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...
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...
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...

