Novel analytical reagent for the application of cloud-point preconcentration and flame atomic absorption spectrometric determination of nickel in natural water samples

• Published in: Journal of hazardous materials Vol. 144; no. 1-2; pp. 126 - 131
• Main Authors: SUVARDHAN, K, REKHA, D, KUMAR, K. Suresh, PRASAD, P. Reddy, KUMAR, J. Dilip, JAYARAJ, B, CHIRANJEEVI, P
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier 01.06.2007
• Subjects: Applied sciences; Chelating Agents - chemistry; Exact sciences and technology; Hydrogen-Ion Concentration; Imines - chemistry; Indicators and Reagents; Nickel - analysis; Nickel - chemistry; Pollution; Polyethylene Glycols - chemistry; Spectrophotometry, Atomic; Surface-Active Agents - chemistry; Water Pollutants, Chemical - analysis; Water Pollutants, Chemical - chemistry; Clouds; Enhancement factor; Surfactant; Flame spectrometry; Analytical reagent; Detection limit; Water samples; Preconcentration; N-quino[8,7-b]azin-5-yl-2,3,5,6,8,9,11,12octahydrobenzo[b] [ 1,4,7,10,13]pentaoxacyclopentadecin-15-yl-methanimine; Nickel; Flame atomic absorption spectrometry (FAAS); Cloud-point extraction- preconcentration (CPE-P); Triton X-114; Flame; Atomic absorption spectrometry
• ISSN: 0304-3894; 1873-3336
• DOI: 10.1016/j.jhazmat.2006.10.001

Cloud-point extraction was applied as a preconcentration of nickel after formation of complex with newly synthesized N-quino[8,7-b]azin-5-yl-2,3,5,6,8,9,11,12octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecin-15-yl-methanimine, and later determined by flame atomic absorption spectrometry (FAAS) using octyl phenoxy polyethoxy ethanol (Triton X-114) as surfactant. Nickel was complexed with N-quino[8,7-b]azin-5-yl-2,3,5,6,8,9,11,12octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecin-15-yl-methanimine in an aqueous phase and was kept for 15 min in a thermo-stated bath at 40 degrees C. Separation of the two phases was accomplished by centrifugation for 15 min at 4000 rpm. The chemical variables affecting the cloud-point extraction were evaluated, optimized and successfully applied to the nickel determination in various water samples. Under the optimized conditions, the preconcentration system of 100 ml sample permitted an enhancement factor of 50-fold. The detailed study of various interferences made the method more selective. The detection limits obtained under optimal condition was 0.042 ngml(-1). The extraction efficiency was investigated at different nickel concentrations (20-80 ngml(-1)) and good recoveries (99.05-99.93%) were obtained using present method. The proposed method has been applied successfully for the determination of nickel in various water samples and compared with reported method in terms of Student's t-test and variance ratio f-test which indicate the significance of present method over reported and spectrophotometric methods at 95% confidence level.