Related Experiment Video
Updated: Jun 28, 2026

08:04
Preparation of Functional Silica Using a Bioinspired Method
Published on: August 1, 2018
Stability of reduced molybdosilicic acids
1Academy of Mining and Metallurgy in Kraków, Institute of Materials Science, Al. Mickiewicza 30, 30-059 Kraków, Poland.
Talanta
|April 1, 1990
Summary
Reduction stabilizes molybdosilicic acids (MSA) in alkaline solutions. Specifically, reducing two or more Mo(VI) atoms to Mo(V) yields stable products, impacting silicon determination methods.
Area of Science:
- Inorganic Chemistry
- Analytical Chemistry
- Solution Chemistry
Background:
- Molybdosilicic acids (MSA) are important heteropoly acids.
- The stability of reduced forms of MSA is crucial for analytical applications.
- Understanding reduction effects is key to accurate silicon determination.
Purpose of the Study:
- To investigate the impact of reduction on the stability of alpha- and beta-molybdosilicic acids (MSA).
- To determine the conditions under which reduced MSA species are stable.
- To explore implications for silicon analysis and purification of MSA isomers.
Main Methods:
- Controlled reduction of molybdosilicic acids (MSA) in alkaline media.
- Spectroscopic analysis to determine the degree of reduction (Mo(VI) to Mo(V)).
- Stability studies at varying temperatures and solution compositions.
Main Results:
- Reduced MSA (≥2 Mo(V) per MSA) exhibit stability in alkaline solutions.
- Beta-MSA reduced to this extent remains stable at higher temperatures, resisting transformation to alpha-MSA.
- Mixtures with apparent reduction <2 Mo(V) are treated as mixtures of unreduced and fully reduced (2 Mo(V)) MSA.
- Unreduced MSA reacts with reduced forms, indicating instability in mixtures with 4 Mo(V) per MSA.
Conclusions:
- The degree of reduction significantly influences MSA stability in alkaline media.
- Specific reduction levels yield stable MSA species, essential for reliable silicon determination.
- A method for isolating pure beta-MSA from mixed solutions was developed based on stability differences.
Related Concept Videos
Stability of Substituted Cyclohexanes
This lesson discusses the stability of substituted cyclohexanes with a focus on energies of various conformers and the effect of 1,3-diaxial interactions.
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
Complexation Equilibria: Factors Influencing Stability of Complexes
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
Molecular Structure and Acidity
An acid can be deprotonated to form a conjugate base or an anion. If the produced anion is more stable, then the acid is stronger. On the contrary, if the anion is unstable, then the acid is weaker. Hence, to determine the acidity of the compound, the stability of its conjugate base is studied using various factors.
The size effect explains the change in atomic size on acidity. When comparing the acids formed from elements that belong to the same column in the periodic table, their atomic sizes...
The size effect explains the change in atomic size on acidity. When comparing the acids formed from elements that belong to the same column in the periodic table, their atomic sizes...
Acid Halides to Alcohols: LiAlH4 Reduction
Acid halides are reduced to alcohols in the presence of a strong reducing agent like lithium aluminum hydride.
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...
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...
Stability of Conjugated Dienes
Introduction
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
Solvating Effects
An understanding of the solvating effect helps rationalize the relation between solvation and acidity of the compound. In addition, this also explains the relative stability of conjugate bases for compounds with different pKa values. This lesson details, in-depth, the principle of solvating effects. The strength of an acid and the stability of its corresponding conjugate base are determined using pKa values. This observed relationship is a consequence of solvation, which is the interaction...

