• Title of article

    Surface Modified Nanomagnetite-Assisted Hollow Fiber Solid/ Liquid Phase Microextraction for Pre-concentration and Determination of Palladium in Water Samples by Differential Pulse Voltammetry

  • Author/Authors

    اسحاقي ، زرين نويسنده , , معين پور، فاطمه نويسنده Department of Chemistry, Faculty of Sciences, Payame Noor University, PO Box 19395-3697, Tehran, Iran Moeinpour, Fatemeh

  • Issue Information
    دوفصلنامه با شماره پیاپی 0 سال 2014
  • Pages
    7
  • From page
    58
  • To page
    64
  • Abstract
    يك روش پيش تغليظ و جداسازي كارآمد موسوم به ميكرو استخراج فاز جامد / مايع با فيبر متخلخل براي تعيين مقادير بسيار كم پالاديوم در نمونه هاي آبي همراه با روش ولتامتري پالسي تفاضلي ارايه شد. در اين روش يك ماده جاذب هيبريدي با استفاده از نانوذرات عاملدار گنجانيده شده در حلال آلي به عنوان فاز استخراج گر مورد استفاده قرار گرفت. نانوذرات پخش شده در حلال آلي در داخل منافذ و مجراي فيبر متخلخل پلي پروپيلن قرارداده شد. اين قطعه فيبر به طور مستقيم با فاز آبي دهنده در تماس بوده است. روش ارايه شده براي تعيين مقدار بسيار كم پالاديوم در نمونه هاي واقعي آب به كار گرفته شد و نتايج رضايت بخشي به دست آمد.
  • Abstract
    An efficient separation-preconcentration procedure namely hollow fiber solid/liquid phase microextraction (HF-SLPME) was developed for determination of trace amounts of palladium in water samples by differential pulse voltammetry. In this method, a hybrid sorbent utilizing functionalized nanoparticles incorporated in an organic solvent was used as the extractor phase. The nanoparticle dis­persed in the organic solvent is held in the pores and lumen of a porous polypropylene hollow fiber. It is in contact directly with the aqueous donor phase. The influence of the various analytical parameters such as pH, kind and amounts of nanoparticle and matrix effects, sample volume, extraction time, etc. were studied for the quantitative recoveries of the analyte ions. Under the optimized experimental conditions, the calibration curves for Pd (II) was linear from 0.1 to 500 ng/mL. The relative standard deviation for seven replicate determinations of 0.1 mg/mL palladium in the standard solutions was 3.95 %. The detection limit based on 3Sb for Pd (II) in the standard solutions was 0.01 ng/mL. The proposed method has been applied for determination of trace amounts of palladium in the real water samples and satisfactory results were obtained.
  • Journal title
    Iranian Journal of Analytical Chemistry
  • Serial Year
    2014
  • Journal title
    Iranian Journal of Analytical Chemistry
  • Record number

    2395725