2009Metallurgical AnalysisRequires access

Determination of trace silicon in water samples by reverse flow injection spectrophotometry

Zhang Xin-shen

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Abstract

The determination of silicon in water by reverse flow injection spectrophotometry was developed using ammonium molybdate as color agent and methylaminophenol-sodium sulfite as reducing agent.The optimized technical conditions of flow injection were as follows: sulfuric acid-oxalic acid as reference solution;the sampling loop volume,250 μL;the lengths of reaction coils for mixing sample and carrying out reaction,both 3 m;the flow rate of sample solution,0.85mL/min;the flow rate of reference solution,color agent and reducing agent,all 0.40 mL/min.Under these optimized experimental conditions,a good calibration curve could be obtained with the linear range of 25-1500 μg/L and detection limit of 21.3 μg/L.200 μg/L Si(Ⅳ) standard solution was determined for 16 times,with the RSD of 2.2 %.The recovery of standard addition for actual water sample was 95 %-105 %.

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The determination of silicon in water by reverse flow injection spectrophotometry was developed using ammonium molybdate as color agent and methylaminophenol-sodium sulfite as reducing agent.The optimized technical conditions of flow injection were as follows: sulfuric acid-oxalic acid as reference solution;the sampling loop volume,250 μL;the lengths of reaction coils for mixing sample and carrying out reaction,both 3 m;the flow rate of sample solution,0.85mL/min;the flow rate of reference solution,color agent and reducing agent,all 0.40 mL/min.Under these optimized experimental conditions,a good calibration curve could be obtained with the linear range of 25-1500 μg/L and detection limit of 21.3 μg/L.200 μg/L Si(Ⅳ) standard solution was determined for 16 times,with the RSD of 2.2 %.The recovery of standard addition for actual water sample was 95 %-105 %.

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Available abstract

The determination of silicon in water by reverse flow injection spectrophotometry was developed using ammonium molybdate as color agent and methylaminophenol-sodium sulfite as reducing agent.The optimized technical conditions of flow injection were as follows: sulfuric acid-oxalic acid as reference solution;the sampling loop volume,250 μL;the lengths of reaction coils for mixing sample and carrying out reaction,both 3 m;the flow rate of sample solution,0.85mL/min;the flow rate of reference solution,color agent and reducing agent,all 0.40 mL/min.Under these optimized experimental conditions,a good calibration curve could be obtained with the linear range of 25-1500 μg/L and detection limit of 21.3 μg/L.200 μg/L Si(Ⅳ) standard solution was determined for 16 times,with the RSD of 2.2 %.The recovery of standard addition for actual water sample was 95 %-105 %.

Key concepts: Spectrophotometry, Chemistry, Sodium sulfite, Flow injection analysis, Volumetric flow rate, Analytical Chemistry (journal), Detection limit, Ammonium molybdate

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