DEVELOPMENT OF FLOW INJECTION ANALYSIS SYSTEM FOR DETERMINATION OF IRON(II) AND TOTAL IRON IN GROUND WATER
Jintana Klamtet
Abstract
Jintana Klamtet
Abstract
A reversed flow injection spectrophotometric determination of iron(II) and total iron has been carried out. It is based on the reaction between iron(II) and 4-(2-pyridylazo)-resorcinol (PAR) in acetate buffer pH 9.0 yielding a yellowish-orange coloured complex with an absorption maximum at 714 nm. The 50 μl of 5×10-4 mol L-1 PAR solution was injected into a continuous flowing stream of 0.01 M HCl with an appropriate flow rate of 0.9 ml min- 1. Then, it was merged with sample solution and acetate buffer flowing at the rate of 2.2 and 2.4 ml min-1, respectively, and the sample zone was detected by spectrophotometer. The optimum conditions of this system were determined. Two linear calibration curves over the concentration range 0.05-3.00 mg L-1 of iron(II) and iron(III) solutions were obtained with the regression equations A=0.176C+0.0128 (r2=0.9988) and A=0.1116C + 0.0018 (r2=0.9966), respectively. A detection limit (defined as 2σ) was 0.012 mg L-1 with a sample throughput of 180 samples h-1. The relative standard deviation was 0..21% (n = 15) at the 3.00 mg L-1 Fe (II). The proposed method was successfully applied to the determination of iron (II) and total iron in groundwater. Analytical results obtained by the proposed method were in good agreement with those obtained by reference methods. Keywords : Flow injection analysis, PAR,Iron
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A reversed flow injection spectrophotometric determination of iron(II) and total iron has been carried out. It is based on the reaction between iron(II) and 4-(2-pyridylazo)-resorcinol (PAR) in acetate buffer pH 9.0 yielding a yellowish-orange coloured complex with an absorption maximum at 714 nm. The 50 μl of 5×10-4 mol L-1 PAR solution was injected into a continuous flowing stream of 0.01 M HCl with an appropriate flow rate of 0.9 ml min- 1. Then, it was merged with sample solution and acetate buffer flowing at the rate of 2.2 and 2.4 ml min-1, respectively, and the sample zone was detected by spectrophotometer. The optimum conditions of this system were determined. Two linear calibration curves over the concentration range 0.05-3.00 mg L-1 of iron(II) and iron(III) solutions were obtained with the regression equations A=0.176C+0.0128 (r2=0.9988) and A=0.1116C + 0.0018 (r2=0.9966), respectively. A detection limit (defined as 2σ) was 0.012 mg L-1 with a sample throughput of 180 samples h-1. The relative standard deviation was 0..21% (n = 15) at the 3.00 mg L-1 Fe (II). The proposed method was successfully applied to the determination of iron (II) and total iron in groundwater. Analytical results obtained by the proposed method were in good agreement with those obtained by reference methods. Keywords : Flow injection analysis, PAR,Iron
Key concepts: Chemistry, Resorcinol, Analytical Chemistry (journal), Detection limit, Flow injection analysis, Volumetric flow rate, Calibration curve, Buffer solution