2022
DOI: 10.1007/s11696-022-02330-w
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Preconcentration of heavy metal ions on magnetic multi-walled carbon nanotubes using magnetic solid-phase extraction and determination in vegetable samples by electrothermal atomic absorption spectrometry: Box–Behnken design

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Cited by 15 publications
(7 citation statements)
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“…The corresponding values for Zn, determined over a period of 6 months using the CRM IRMM-3702 and CRM IRMM-651, were d 66 Zn 3702 : 0.00 ± 0.02& (n = 15) and d 66 Zn 3702 : −11.6 ± 0.03& (n = 8). Measurements of the207 Pb :206 Pb and208 Pb :206 Pb ratios in NIST SRM 981 yielded the values (±2 SD, n = 36) of 0.9145 ± 0.0003 and 2.1661 ± 0.0004 (2 SD, n = 36), respectively, reported as being in good agreement with other literature values. Copper, Pb and Zn isotope data in RMs were obtained from four replicate analysis of each material.…”
supporting
confidence: 87%
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“…The corresponding values for Zn, determined over a period of 6 months using the CRM IRMM-3702 and CRM IRMM-651, were d 66 Zn 3702 : 0.00 ± 0.02& (n = 15) and d 66 Zn 3702 : −11.6 ± 0.03& (n = 8). Measurements of the207 Pb :206 Pb and208 Pb :206 Pb ratios in NIST SRM 981 yielded the values (±2 SD, n = 36) of 0.9145 ± 0.0003 and 2.1661 ± 0.0004 (2 SD, n = 36), respectively, reported as being in good agreement with other literature values. Copper, Pb and Zn isotope data in RMs were obtained from four replicate analysis of each material.…”
supporting
confidence: 87%
“…Recovery aer the separation process, evaluated from eight RMs, was 99.2%. Comparison of the208 Pb :206 Pb and207 Pb :206 Pb values of the reference solution NIST SRM 981 analysed with or without the chemical separation step did not show evidence of isotope fractionation. AE647 and CRM ERM-AE633, were d 65 Cu AE647 : 0.00 ± 0.02& (n = 54) and d 65 Cu AE647 : −0.21 ± 0.03& (n = 33).…”
mentioning
confidence: 84%
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“…Currently, methods for detecting heavy metals can be categorised as instrumental analysis and rapid detection methods. Instrumental methods, such as electrothermal atomic absorption spectrometry (ET‐AAS; Khodadadi et al ., 2022), graphite furnace atomic absorption spectrometry (GFAAS; Ge et al ., 2020), atomic absorption spectrometry (AAS; Peter et al ., 2012), laser‐induced breakdown spectroscopy (LIBS; Wang et al ., 2020b), X‐ray fluorescence (XRF; Farahani et al ., 2015), inductively coupled plasma mass spectrometry (ICP‐MS) and inductively coupled plasma optical emission spectrometry (ICP‐OES; El Chafic et al ., 2013), offer high sensitivity, low detection limits, minimal spectral interference and a wide linear range (Planeta et al ., 2021). However, their use for real‐time and on‐site monitoring is limited due to their dependence on expensive equipment, specialised procedures, intricate sample preparation and time‐consuming analysis (Klotz et al ., 2013).…”
Section: Introductionmentioning
confidence: 99%