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Separation and preconcentration of cadmium ions in natural water using a liquid membrane system with 2-acetylpyridine benzoylhydrazone as carrier by flame atomic absorption spectrometry
Institution:1. Department of Energy and Mechanical Engineering, The Institute of Marine Industry, Cheondaegukchi-Gil 38, Tongyeong, Gyeongnam 650-160, South Korea;2. School of Chemical Engineering, The University of Adelaide, Adelaide, SA 5005, Australia;3. Department of Biomedical Engineering, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur, Malaysia;1. School of Chemical Sciences, Universiti Sains Malaysia (USM), 11800 Minden, Pulau Pinang, Malaysia;2. School of Chemical Sciences & Food Technology, Faculty of Science & Technology, Universiti Kebangsaan Malaysia (UKM), 43600 Bangi, Selangor, Malaysia;3. Faculty of Science & Technology, Universiti Sains Islam Malaysia (USIM), Bandar Baru Nilai, 71800 Nilai, Negeri Sembilan, Malaysia
Abstract:A method for the determination of Cd in natural water by flame atomic absorption spectrometry after separation and preconcentration with a bulk liquid membrane containing 2-acetylpyridine benzoylhydrazone as mobile carrier dissolved in toluene has been developed. Effects of carrier concentration, volume of organic phase and pH of feed and receiving solutions on the flux for Cd across the membrane have been studied, being optimized by the modified simplex method. Optimum values for these variables were: carrier concentration of 0.84 g l?1, 74 ml of toluene, pH 7.8 in the feed solution and 0.06 mol l?1 of HNO3 in the receiving solution, allowing a preconcentration factor of 17.9. The preconcentration step required 7 h to be accomplished. The recovery of Cd at optimum conditions was 101.0±2.7%, even with saline matrix, with good relative standard deviation (2.5%) at 95% confidence level. The detection limit of blank sample was 6 ng l?1 of Cd. The method was validated using a certified reference material (TMDA-62) and also applied successfully to the analysis of Cd in four samples of seawater collected from the coast of Huelva (Spain). The relative errors of determinations were ?7.6% for certified reference material and ranging between +2.4 and +7.1%, for samples of seawater (obtained between the results of the proposed and differential pulse anodic stripping voltammetry methods).
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