Determination of vanadium (V) in drinking water by flow injection and pre-concentration in a knotted reactor by inductively coupled plasma optical emission spectrometry with ultrasonic nebulization

An on-line vanadium pre-concentration and determination system implemented with inductively coupled plasma optical emission spectrometry (ICP-OES) associated with a flow injection (FI) method with ultrasonic nebulization (USN) system was studied, The vanadium was retained as vanadium-2-(5-bromo-2-pyridylazo)-5-diethylaminophenol V(V)-(5-Br-PADAP) complex, at pH 3.2. The vanadium complex was removed from the knotted reactor (KR) with 30% v/v nitric acid, A sensitivity enhancement factor of 180 was obtained with respect to ICP-OES using pneumatic nebulization (15 for USN and 12 for KR). The value of detection limit for the pre-concentration of 10 mi of aqueous solution was 19 ng 1(-1). The precision for 10 replicate determinations at the 5 mu g 1(-1) V(V) level was 2.6% relative standard deviation (R.S.D.), calculated with the peak heights obtained. The calibration graph using the pre-concentration system for vanadium was linear with a correlation coefficient of 0.9995 at levels near the detection limits up to at least 100 mu g 1(-1). The method was successfully applied to the determination of vanadium in drinking water samples, (C) 2000 Elsevier Science B.V. All rights reserved.An on-line vanadium pre-concentration and determination system implemented with inductively coupled plasma optical emission spectrometry (ICP-OES) associated with a flow injection (FI) method with ultrasonic nebulization (USN) system was studied, The vanadium was retained as vanadium-2-(5-bromo-2-pyridylazo)-5-diet V(V)-(5-Br-PADAP) complex, at pH 3.2. The vanadium complex was removed from the knotted reactor (KR) with 30% v/v nitric acid, A sensitivity enhancement factor of 180 was obtained with respect to ICP-OES using pneumatic nebulization (15 for USN and 12 for KR). The value of detection limit for the pre-concentration of 10 mi of aqueous solution was 19 ng 1(-1). The precision for 10 replicate determinations at the 5 mu g 1(-1) V(V) level was 2.6% relative standard deviation (R.S.D.), calculated with the peak heights obtained. The calibration graph using the pre-concentration system for vanadium was linear with a correlation coefficient of 0.9995 at levels near the detection limits up to at least 100 mu g 1(-1). The method was successfully applied to the determination of vanadium in drinking water samples, (C) 2000 Elsevier Science B.V. All rights reserved.