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Perxanthate determination in flotation solutions by ultraviolet spectrophotometry
1CSIRO Division of Mineral Chemistry, P.O. Box 124, Port Melbourne, Victoria 3207, Australia.
Talanta
|September 1, 1979
Summary
Alkyl perxanthates can be quantified in solutions using ultraviolet spectrophotometry, either directly or after solvent extraction. This method offers a reliable detection limit of 0.2 mg/l for accurate analysis.
Area of Science:
- Analytical Chemistry
- Spectroscopy
- Mineral Processing
Background:
- Alkyl perxanthates are crucial reagents in mineral flotation.
- Accurate quantification of alkyl perxanthates is essential for process control and optimization.
- Existing analytical methods may have limitations in complex industrial matrices.
Purpose of the Study:
- To develop and validate a robust spectrophotometric method for determining alkyl perxanthates.
- To compare direct spectrophotometry with solvent extraction for perxanthate analysis.
- To establish the analytical parameters, including molar absorptivity and detection limits.
Main Methods:
- Direct ultraviolet spectrophotometry of alkaline solutions (pH > 8) at 348 nm.
- Solvent extraction into chloroform after acidification (pH < 2).
- Spectrophotometric analysis of the organic extract at 302 nm.
Main Results:
- Direct method: molar absorptivity of 1.042 x 10^4 l.mole^-1.cm^-1, Beer's law up to 25 mg/l, detection limit 0.2 mg/l.
- Extraction method: molar absorptivity of 5.47 x 10^3 l.mole^-1.cm^-1, Beer's law up to 25 mg/l, detection limit 0.2 mg/l.
- Minimal interferences observed for both methods, with specific thresholds noted for nickelocyanide, mercaptobenzothiazole, sodium sulphite, and cuprocyanide.
Conclusions:
- Both direct and extraction-based UV spectrophotometry are effective for alkyl perxanthate determination.
- Direct method is suitable for clear solutions, while extraction enhances applicability for complex matrices.
- The validated methods provide accurate and sensitive quantification of alkyl perxanthates in industrial settings.
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