Determination of Cu(2+), Zn(2+) and Pb(2+) in biological and food samples by FAAS after preconcentration with hydroxyapatite nanorods originated from eggshell

• Published in: Materials science & engineering. C, Materials for biological applications Materials for biological applications, 2015, Vol.52, p.288-296
• Main Authors: Mortada, Wael I, Kenawy, Ibrahim M M, Abdelghany, Amr M, Ismail, Amani M, Donia, Ahmed F, Nabieh, Kareem A
• Format: Article
• Language: English
• Subjects: Copper - analysis; Durapatite - chemistry; Lead - analysis; Nanotubes - chemistry; Solid Phase Extraction; Spectrophotometry, Atomic; Zinc - analysis
• ISSN: 1873-0191
• DOI: 10.1016/j.msec.2015.03.061

Hydroxyapatite nanorods (HAPNRs) were prepared from recycled eggshell by using precipitation method. The structure of the HAPNRs was physicochemically and morphologically characterized by X-ray diffraction, transmission electron microscopy and Fourier transform infrared spectroscopy. The resulting HAPNRs were used for solid phase extractive preconcentration of Cu(2+), Zn(2+) and Pb(2+) prior to its determination by flame atomic absorption spectrometry. Experimental variables that influence the quantitative extraction of metal ions were optimized by both batch and column methods. The analytes were quantitatively sorbed on the matrix between pHs6 and 9. The maximum sorption capacity of the HAPNRs has been found to be 2.43, 2.37 and 2.53 mmol g(-1) for Cu(2+), Zn(2+) and Pb(2+), respectively, with the preconcentration factor of 250. The 3σ detection limit and 10σ quantification limit for Cu(2+), Zn(2+) and Pb(2+) were found to be 0.72, 0.55 and 5.12 μg L(-1) and 2.40, 1.83 and 17.06 μg L(-1), respectively. The calibration curves were linear up to 250 μg L(-1) for Cu(2+), 300 μg L(-1) for Zn(2+) and 400 μg L(-1) for Pb(2+). Accuracy of the proposed method was verified using certified reference materials (NCS ZC85006 Tomato, Seronorm Trace Elements Whole Blood L-1, Seronorm Trace Elements Whole Blood L-3 and Seronorm Trace Elements Urine). The present method was successfully applied to the analysis of these metal ions in sea water, biological and food samples.