scholarly journals A Sequential Injection System for the Spectrophotometric Determination of Calcium, Magnesium and Alkalinity in Water Samples

2004 ◽  
Vol 20 (8) ◽  
pp. 1205-1210 ◽  
Author(s):  
Raquel B. R. MESQUITA ◽  
António O. S. S. RANGEL
2005 ◽  
Vol 88 (2) ◽  
pp. 639-644 ◽  
Author(s):  
Inês P A Morais ◽  
M Renata S Souto ◽  
António O S S Rangel

Abstract A double-line sequential injection system was developed for the spectrophotometric determination of several metal ions in waters. The proposed double-line configuration was used to enable adding sample and chromogenic reagents as merging zones. The methodology was applied to the spectrophotometric determination of copper, iron, manganese, and zinc in samples of diverse origins at the range of 0.15–5.00, 0.10–10.0, 0.48–4.00, and 0.11–5.00 mg/L, respectively. Different chromogenic reagents and detection wavelengths were used. The chromogenic reagents for iron and manganese were 1,10-phenanthroline and formaldoxime, respectively. Copper and zinc were both determined using the analytical reagent zincon. Analytical characteristics of the methodology, such as manifold parameters, buffer pH, and reagent concentrations were optimized, and interference of some of the metal ions commonly present in water sample was assessed. Results of the analysis were in agreement with those obtained by atomic absorption spectrometry. Repeatability, expressed as the relative standard deviation for 10 consecutive injections of water samples, was lower than 6%. The determination rate was approximately 36/h.


2020 ◽  
Vol 12 (6) ◽  
pp. 855-864 ◽  
Author(s):  
Wanpen Khongpet ◽  
Pattama Yanu ◽  
Somkid Pencharee ◽  
Chanida Puangpila ◽  
Supaporn Kradtap Hartwell ◽  
...  

A miniaturized microfluidic hydrodynamic sequential injection system for sensitive colorimetric detection was developed for performance improvement in the measurement of phosphate, nitrite, and nitrate based on molybdenum blue and Griess methods.


2001 ◽  
Vol 84 (2) ◽  
pp. 337-341 ◽  
Author(s):  
José Antonio Erustes ◽  
Rarel Forteza ◽  
Victor Cerdà

Abstract A novel sequential-injection system was developed for determination of iodide at very low concentrations by using a kinetic method. The method is based on the catalytic effect of iodide on the redox reaction between Ce4+ and As3+ first described by Sandell and Kolthoff. The calibration curve is constructed by measuring the decrease of Ce4+ absorbance versus iodide concentration with a delay time of 30 s. The detection limit is 1.5 μg/L, the working temperature is 45°C, and the working range is 0.002–0.5 mg/L. Reasonable agreement was obtained when the method was applied to pharmaceutical and drinking water samples. The method has a sample throughput of approximately 15/h.


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