Determination of toxic elements in plastics from waste electrical and electronic equipment by slurry sampling electrothermal atomic absorption spectrometry

Author(s)

Santos, Mirian C. ^[1] ; Nobrega, Joaquim A. ^[2] ; Baccan, Nivaldo ^{[1, 3]} ; Cadore, Solange ^[1]

Affiliation

^[1] Univ Estadual Campinas, Inst Chem, BR-13083970 Campinas, SP - Brazil

^[2] Univ Fed Sao Carlos, Dept Quim, Grp Anal Instrumental Aplicada, BR-13560 Sao Carlos, SP - Brazil

^[3] Fac Paulinia, BR-13140000 Paulinia, SP - Brazil

• Document type: Journal article
• Source: Talanta; v. 81, n. 4-5, p. 1781-1787, JUN 15 2010.
• Web of Science Citations: 25

Abstract

Cadmium, chromium, lead and antimony were determined in slurries prepared using pulverized samples of personal computers and mobile phones dispersed in dimethylformamide medium. Determinations were carried out by electrothermal atomic absorption spectrometry (ETAAS) using a graphite furnace atomic absorption spectrometer The optimization of the experimental conditions (chemical modifier. pyrolysis time, pyrolysis temperature and atomization temperatures) was accomplished by evaluating pyrolysis and atomization curves. Optimization was also used to determine the temperatures corresponding to the best sensitivities and the lowest background signals The pyrolysis temperatures were Fixed at 600 degrees C (for Cd), 700 degrees C (for Pb), 1100 degrees C (for Sb), and 1200 degrees C (for Cr), atomization temperatures were established as 1400 degrees C (for Cd), 1300 degrees C (for PI)), 1900 degrees C (for Sb). and 2300 degrees C (for Cr), and the chemical modifier (50 mu g NH(4)H(2)PO(4) + 3 mu g Mg(NO(3))(2) was used for Cd and Pb while 5 mu g Pd + 3 mu g Mg(NO(3))(2) was used for Sb) The use of a chemical modifier for Cr determination was not necessary. The characteristic masses were 1 9 pg for Cd, 32.3 pg for Pb, 54.1 pg for Sb, and 9.1 pg for Cr, Calibration was performed using standard additions in a range of 5-20 mu g L(-1) for Cd, 5-30 mu g L(-1) for Cr, 12 5-50 mu g L(-1) for Pb, and 25-100 mu g L(-1) for Sb with linear correlation coefficients higher than 0.99 Limits of detection were 0 9, 1.4, 6.8, and 2.9 mu g L(-1) for Cd. Pb, Sb, and Cr. respectively. The results indicate that recoveries for all metals agreed at a 95% confidence level when a paired t-test was applied and presented good precision The accuracy of the proposed method was evaluated by addition-recovery experiments, showing results in the 96-112% range, and also by comparison of the results using Student's t-test with another method developed using ETAAS for digested samples Analyte concentrations in the samples investigated varied from 5 to 525, 51 to 611, and 30 to 458 mg kg(-1) for Cd, Cr, and Pb. respectively, while the content of SI) was in the 02-1 65% range. (C) 2010 Elsevier B V All rights reserved (AU)