TY - JOUR
T1 - Magnetic extraction and preconcentration of perfluorooctanoic acid in aqueous solutions using magnetic tea waste activated carbon
AU - Malatji, Nompumelelo
AU - Mpupa, Anele
AU - Mizaikoff, Boris
AU - Nomngongo, Philiswa Nosizo
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2026/5
Y1 - 2026/5
N2 - This study developed a method to determine perfluorooctanoic acid in real water samples using ultra-high performance liquid chromatography-electrospray-tandem mass spectrometry after dispersive magnetic solid phase extraction. The adsorbent used in dispersive magnetic solid phase extraction was tea waste activated carbon modified with magnetic nanoparticles. Successful synthesis of the adsorbent was confirmed by Fourier Transform infrared spectroscopy, X-ray diffraction, and energy-dispersive X-ray spectroscopy. The morphological and surface properties were investigated using scanning and transmission electron microscopy. Various experimental factors affecting the extraction and preconcentration efficiency were optimised using the design of experiments. Under the optimised conditions, the developed method had a wide linear range (39-5000 ng/L) with a correlation coefficient of 0.9915. The limit of detection was 11.7 ng/L, whereas the limit of quantification was 39.0 ng/L. The precision in terms of repeatability (intraday, n = 4 replicates) and reproducibility (interday, n = 3 days) expressed as %RSD were 2.40% and 3.10% respectively, which indicated that the developed method had good precision. The trueness of the developed method was investigated using a spike recovery test, and percentage recoveries ranged from 88.2% to 98.4 %. The magnetic activated carbon adsorbent could be reused up to 4 cycles. The developed method was successfully applied to detect perfluorooctanoic acid in three river water samples. Finally, the extent of greenness of the developed method was evaluated using six metric tools, and the findings showed that the method was environmentally friendly, cost-effective, highly practical and applicable.
AB - This study developed a method to determine perfluorooctanoic acid in real water samples using ultra-high performance liquid chromatography-electrospray-tandem mass spectrometry after dispersive magnetic solid phase extraction. The adsorbent used in dispersive magnetic solid phase extraction was tea waste activated carbon modified with magnetic nanoparticles. Successful synthesis of the adsorbent was confirmed by Fourier Transform infrared spectroscopy, X-ray diffraction, and energy-dispersive X-ray spectroscopy. The morphological and surface properties were investigated using scanning and transmission electron microscopy. Various experimental factors affecting the extraction and preconcentration efficiency were optimised using the design of experiments. Under the optimised conditions, the developed method had a wide linear range (39-5000 ng/L) with a correlation coefficient of 0.9915. The limit of detection was 11.7 ng/L, whereas the limit of quantification was 39.0 ng/L. The precision in terms of repeatability (intraday, n = 4 replicates) and reproducibility (interday, n = 3 days) expressed as %RSD were 2.40% and 3.10% respectively, which indicated that the developed method had good precision. The trueness of the developed method was investigated using a spike recovery test, and percentage recoveries ranged from 88.2% to 98.4 %. The magnetic activated carbon adsorbent could be reused up to 4 cycles. The developed method was successfully applied to detect perfluorooctanoic acid in three river water samples. Finally, the extent of greenness of the developed method was evaluated using six metric tools, and the findings showed that the method was environmentally friendly, cost-effective, highly practical and applicable.
KW - Activated carbon
KW - Perfluoroalkyl substances
KW - Perfluorooctanoic acid
KW - Preconcentration
KW - Solid phase extraction
UR - https://www.scopus.com/pages/publications/105022289454
U2 - 10.1016/j.jcoa.2025.100290
DO - 10.1016/j.jcoa.2025.100290
M3 - Article
AN - SCOPUS:105022289454
SN - 2772-3917
VL - 9
JO - Journal of Chromatography Open
JF - Journal of Chromatography Open
M1 - 100290
ER -