Development of simple pocket test tools for fast determination of dissolved sulfate in waters

Citation
Vm. Ostrovskaya et al., Development of simple pocket test tools for fast determination of dissolved sulfate in waters, FIELD A C T, 4(2-3), 2000, pp. 147-153
Citations number
4
Categorie Soggetti
Environment/Ecology,"Spectroscopy /Instrumentation/Analytical Sciences","Instrumentation & Measurement
Journal title
FIELD ANALYTICAL CHEMISTRY AND TECHNOLOGY
ISSN journal
1086900X → ACNP
Volume
4
Issue
2-3
Year of publication
2000
Pages
147 - 153
Database
ISI
SICI code
1086-900X(2000)4:2-3<147:DOSPTT>2.0.ZU;2-Y
Abstract
A rapid field method for routine checks on dissolved sulfate in surface, ru nning, and potable waters is presented. The method uses reagent indicator p aper strips and a thermometric unit. The RIS-Sulfate-Test was developed by immobilization of an Arsenate III-barium complex together with buffer and m asking reagents on cellulose paper. It was adapted to sulfate-ion determina tion with the use of visual, densitometric, and photometric techniques, the lower detection limit being 0.05-0.1 g L-1. The sensing principle is based on the reaction, which gives a colorless barium sulfate precipitate with a heat of formation of Delta H = 4.6 kcal M-1. After the strip is immersed i nto a sample solution for 1 s, the color changes from black-blue to pink-vi olet because of sulfate-induced complex decomposition. Color changes are mo nitored with the use of a standard color scale and a miniaturized reflectom eter with 660-nm light diode. A miniaturized calorimeter was used for deter mining high concentrations of sulfate. A 0.3-ml aliquot of sample solution is placed on the bottom of a 5-ml polyethylene vessel, and 0.1-0.2 ml of 0. 3-M barium chloride is introduced into the vessel with a 1-ml syringe. The lower part of the syringe with the reagent is immersed into the sample solu tion for a quicker thermal equilibration. After 10 min, the reagent is inje cted into the solution and readings are taken with a small voltmeter. A lin ear dependence of the instrument readings on sulfate concentration was obse rved in the 0.2 to 5-g L-1 range (P = 0.95, n = 3, RSD = 20%). Both methods were checked by standard addition and dilution procedures, and their relia bility was confirmed by flow-injection analysis of seawater with the use of spectrophotometric detection of a turbidimetric indicator reaction. (C) 20 00 John Wiley & Sons, Inc.