Victor Barreto

New membrane-based electrolytic suppressor device for suppressed conductivity detection in ion chromatography

Abstract This paper discusses the newest advancement in chemical suppression preceding conductivity detection. The new suppressor uses electrolysis of deionized water to generate the required acid or base for the suppression neutralization reaction and utilizes the electrical field to enhance, through electrodialysis, the suppressors capacity for neutralization. The suppressor is able to accommodate eluents as high as 150 mM NaOH, without the need for a separate regenerant solution, by recycling the conductivity detector cell waste to the regenerant and electrolysing the water in the waste stream to the required acid or base. The device is able to use deionized water as regenerant and neutralize the eluent stream to deionized water without the expected increase in resistance by employing ion exchange material in intimate contact with the electrodes and the membranes. The current is carried with low resistance through the ion-exchange material via ion transport from one ion-exchange site to another.

Capillary ion chromatography

This review summarizes progress in capillary ion chromatography. Theoretical aspects and practical limitations of packed and open tubular capillary columns are considered. Applications of packed and open tubular capillary IC are described. Emerging technologies such chip-scale IC and the use of monolithic columns are discussed.

Determination of anions at trace levels in power plant water samples by ion chromatography with electrolytic eluent generation and suppression

An ion chromatographic method was developed for the determination of nine inorganic and organic acid anions at sub- to low-microg/l levels in power plant water samples. In this method, samples were injected using a large-volume direct injection technique, the analyte anions were separated on a hydroxide-selective anion-exchange column using high-purity hydroxide eluents generated by an on-line electrolytic eluent generator and detected using the suppressed conductivity detection method. The method performance was evaluated by analyzing synthetic water samples containing additives encountered in the power plant water samples and four water samples from a fossil fuel power plant. The relative standard deviations of retention times of analyte ions separated on the hydroxide-selective anion-exchange column were less than 0.4%. The recoveries of analyte ions spiked into the synthetic water samples at concentrations of 0.13-1.0 microg/l were in the range of 70-120%. The method detection limits for analyte ions in deionized water were 0.0099, 0.0056, 0.019, 0.057, 0.0084, 0.023, 0.067, 0.037, and 0.079 microg/l for fluoride, acetate, formate, chloride, nitrite, sulfate, bromide, nitrate, and phosphate, respectively.