Determination of Inorganic Cations and Ammonium in Environmental Waters Using a Compact, Integrated, High-Pressure Ion Chromatography System
Applications | 2016 | Thermo Fisher ScientificInstrumentation
The determination of inorganic cations and ammonium in environmental waters is essential for regulatory compliance, water quality assessment and corrosion control in distribution systems.
This work aims to evaluate a compact high-pressure ion chromatography system equipped with a 4-µm particle cation exchange column for rapid and sensitive quantification of alkali and alkaline earth cations along with ammonium in drinking water, wastewater and acidic soil extracts.
The analysis employed the Thermo Scientific Dionex Integrion HPIC system with Reagent-Free™ IC technology, an automated eluent generator cartridge (EGC 500 MSA) and a Thermo Scientific Dionex IonPac CS16-4 µm column set. PEEK Viper™ fittings and a suppressed conductivity detector were used to enhance reproducibility and sensitivity.
Samples were filtered through 0.2 µm syringe filters prior to injection. Soil extracts were prepared by sonicating 3 g of soil with 30 mL of 30 mM methanesulfonic acid, followed by centrifugation and filtration.
Chromatographic conditions included a 4 mm IonPac CS16-4 µm column, 30 mM MSA eluent generated in situ, a 0.9 mL/min flow rate, column temperature of 40 °C and a 10 µL injection volume. The detector compartment was maintained at 15 °C with suppressed conductivity detection.
Retention times of the six analytes were well separated in under 19 minutes at 0.9 mL/min. Temperature influenced cation selectivity, particularly potassium, highlighting the need for tight temperature control for reproducible retention. Flow rate optimization up to 1.0 mL/min reduced run times without compromising resolution. Calibration was linear over three orders of magnitude for all cations except ammonium, where a quadratic fit extended the range to 40 mg/L. Method detection limits were in the low µg/L range. The system resolved trace ammonium in the presence of 10 000-fold higher sodium concentrations and handled acidic soil extracts without pH adjustment.
Advancements may include coupling with mass spectrometry or optical detectors for multi-mode analysis, further miniaturization for field-deployable systems, online monitoring capabilities and automated workflows to support high-throughput environmental and industrial analytics.
Integrating high-pressure ion chromatography with 4 µm-particle columns and reagent-free eluent generation enables fast, sensitive and reproducible analysis of inorganic cations and ammonium in diverse environmental samples. The method supports regulatory monitoring, water quality control and industrial process analysis.
Ion chromatography
IndustriesEnvironmental
ManufacturerThermo Fisher Scientific
Summary
Importance of the Topic
The determination of inorganic cations and ammonium in environmental waters is essential for regulatory compliance, water quality assessment and corrosion control in distribution systems.
Objectives and Study Overview
This work aims to evaluate a compact high-pressure ion chromatography system equipped with a 4-µm particle cation exchange column for rapid and sensitive quantification of alkali and alkaline earth cations along with ammonium in drinking water, wastewater and acidic soil extracts.
Used Instrumentation
The analysis employed the Thermo Scientific Dionex Integrion HPIC system with Reagent-Free™ IC technology, an automated eluent generator cartridge (EGC 500 MSA) and a Thermo Scientific Dionex IonPac CS16-4 µm column set. PEEK Viper™ fittings and a suppressed conductivity detector were used to enhance reproducibility and sensitivity.
Methodology and Instrumentation
Samples were filtered through 0.2 µm syringe filters prior to injection. Soil extracts were prepared by sonicating 3 g of soil with 30 mL of 30 mM methanesulfonic acid, followed by centrifugation and filtration.
Chromatographic conditions included a 4 mm IonPac CS16-4 µm column, 30 mM MSA eluent generated in situ, a 0.9 mL/min flow rate, column temperature of 40 °C and a 10 µL injection volume. The detector compartment was maintained at 15 °C with suppressed conductivity detection.
Main Results and Discussion
Retention times of the six analytes were well separated in under 19 minutes at 0.9 mL/min. Temperature influenced cation selectivity, particularly potassium, highlighting the need for tight temperature control for reproducible retention. Flow rate optimization up to 1.0 mL/min reduced run times without compromising resolution. Calibration was linear over three orders of magnitude for all cations except ammonium, where a quadratic fit extended the range to 40 mg/L. Method detection limits were in the low µg/L range. The system resolved trace ammonium in the presence of 10 000-fold higher sodium concentrations and handled acidic soil extracts without pH adjustment.
Benefits and Practical Applications
- Rapid analysis with total run times below 24 minutes
- Sensitive quantification of cations and ammonium across a wide concentration range
- Robust performance in matrices with high ionic strength and acidic extracts
- Improved peak efficiency from small-particle column technology
Future Trends and Potential Applications
Advancements may include coupling with mass spectrometry or optical detectors for multi-mode analysis, further miniaturization for field-deployable systems, online monitoring capabilities and automated workflows to support high-throughput environmental and industrial analytics.
Conclusion
Integrating high-pressure ion chromatography with 4 µm-particle columns and reagent-free eluent generation enables fast, sensitive and reproducible analysis of inorganic cations and ammonium in diverse environmental samples. The method supports regulatory monitoring, water quality control and industrial process analysis.
References
- Jackson P.E. Ion Chromatography in Environmental Analysis. In Encyclopedia of Analytical Chemistry; Meyers R.A., ed.; John Wiley & Sons, Chichester, U.K., 2000; pp 2779–2801.
- World Health Organization. Hardness in Drinking-water; Background Document for Development of WHO Guidelines for Drinking-water Quality, Geneva, Switzerland, 2011.
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