Standardization of sodium thiosulfate
Applications | 2025 | MetrohmInstrumentation
The accurate standardization of sodium thiosulfate solutions at low concentrations (0.01 and 0.002 mol/L) is critical for precise iodometric titrations and other redox analyses in quality control, environmental monitoring, and pharmaceutical applications. Ensuring reliable titrant titer minimizes systematic errors and enhances confidence in analytical results across diverse laboratory settings.
This application note presents a detailed protocol for the determination of sodium thiosulfate titrant concentration at 0.01 and 0.002 mol/L. It outlines challenges associated with low-concentration titrants—such as sluggish electrode response and overtitration risks—and demonstrates how to optimize potentiometric titration parameters to obtain reproducible “S”-shaped titration curves using an OMNIS Titrator and Pt Titrode.
Preparation of titrant solutions and auxiliary reagents was carried out using analytical-grade chemicals. For each target concentration, a known volume of potassium iodate standard (0.01 mol/L or 0.002 mol/L) was pipetted into the titration vessel, followed by addition of potassium iodide and sulfuric acid to generate iodine in situ.
The titrant addition was controlled to reach a clear potentiometric endpoint near 6 mL of thiosulfate. Titration parameters were set with a drift limit of 30 mV/min, a minimum dosing increment of 20 µL, and a maximum increment of 150 µL to smooth the titration curve and avoid overshooting.
For 0.002 mol/L sodium thiosulfate (n = 5), the average titer was determined as 2.008 mmol/L with an absolute standard deviation of 0.013 mmol/L (0.6 % RSD). For 0.01 mol/L titrant, the mean value was 10.057 mmol/L with a 0.041 mmol/L deviation (0.4 % RSD). The high reproducibility and low relative error highlight the suitability of potentiometric titration under the optimized conditions for dilute thiosulfate solutions.
Advancements may include integration of flow-through systems to further improve response times at low concentrations, expanded software routines for automated endpoint detection, and broader application of ultra-low-volume dispensing technologies. Coupling potentiometric titration with spectrophotometric detectors could also open new avenues for multi-signal endpoint confirmation.
The described protocol demonstrates that the OMNIS Titrator with Pt Titrode delivers accurate and reproducible titer determinations for sodium thiosulfate at challenging low concentrations. Careful optimization of titration increments, drift limits, and sample handling ensures consistent potentiometric endpoints, supporting reliable analytical workflows.
No external literature references were cited in the original application note.
Electrochemistry, Titration
IndustriesPharma & Biopharma
ManufacturerMetrohm
Summary
Importance of the Topic
The accurate standardization of sodium thiosulfate solutions at low concentrations (0.01 and 0.002 mol/L) is critical for precise iodometric titrations and other redox analyses in quality control, environmental monitoring, and pharmaceutical applications. Ensuring reliable titrant titer minimizes systematic errors and enhances confidence in analytical results across diverse laboratory settings.
Objectives and Study Overview
This application note presents a detailed protocol for the determination of sodium thiosulfate titrant concentration at 0.01 and 0.002 mol/L. It outlines challenges associated with low-concentration titrants—such as sluggish electrode response and overtitration risks—and demonstrates how to optimize potentiometric titration parameters to obtain reproducible “S”-shaped titration curves using an OMNIS Titrator and Pt Titrode.
Methodology
Preparation of titrant solutions and auxiliary reagents was carried out using analytical-grade chemicals. For each target concentration, a known volume of potassium iodate standard (0.01 mol/L or 0.002 mol/L) was pipetted into the titration vessel, followed by addition of potassium iodide and sulfuric acid to generate iodine in situ.
The titrant addition was controlled to reach a clear potentiometric endpoint near 6 mL of thiosulfate. Titration parameters were set with a drift limit of 30 mV/min, a minimum dosing increment of 20 µL, and a maximum increment of 150 µL to smooth the titration curve and avoid overshooting.
Instrumentation Used
- OMNIS Professional Titrator equipped with magnetic stirrer
- Digital Pt Titrode (combined platinum ring electrode with reference)
- 20 mL OMNIS cylinder unit
- Macro pipettes for accurate aliquoting
Key Results and Discussion
For 0.002 mol/L sodium thiosulfate (n = 5), the average titer was determined as 2.008 mmol/L with an absolute standard deviation of 0.013 mmol/L (0.6 % RSD). For 0.01 mol/L titrant, the mean value was 10.057 mmol/L with a 0.041 mmol/L deviation (0.4 % RSD). The high reproducibility and low relative error highlight the suitability of potentiometric titration under the optimized conditions for dilute thiosulfate solutions.
Benefits and Practical Applications
- Enhanced precision for low-level redox titrations in environmental and industrial laboratories.
- Reduction of weighing errors through use of macro pipettes for dilution.
- Flexible OMNIS platform enabling parallel titrations and automation for routine quality control.
Future Trends and Potential Applications
Advancements may include integration of flow-through systems to further improve response times at low concentrations, expanded software routines for automated endpoint detection, and broader application of ultra-low-volume dispensing technologies. Coupling potentiometric titration with spectrophotometric detectors could also open new avenues for multi-signal endpoint confirmation.
Conclusion
The described protocol demonstrates that the OMNIS Titrator with Pt Titrode delivers accurate and reproducible titer determinations for sodium thiosulfate at challenging low concentrations. Careful optimization of titration increments, drift limits, and sample handling ensures consistent potentiometric endpoints, supporting reliable analytical workflows.
References
No external literature references were cited in the original application note.
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