Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.aca.2014.01.022
Title: Evaluation of a cloud point extraction approach for the preconcentration and quantification of trace CuO nanoparticles in environmental waters
Authors: Majedi, S.M.
Kelly, B.C. 
Lee, H.K. 
Keywords: Adsorption
Cloud point extraction
Copper(II) oxide nanoparticle
Dissolution
Environmental water analysis
NP-micelle assembly
Issue Date: 3-Mar-2014
Citation: Majedi, S.M., Kelly, B.C., Lee, H.K. (2014-03-03). Evaluation of a cloud point extraction approach for the preconcentration and quantification of trace CuO nanoparticles in environmental waters. Analytica Chimica Acta 814 : 39-48. ScholarBank@NUS Repository. https://doi.org/10.1016/j.aca.2014.01.022
Abstract: The cloud point extraction (CPE) of commercial copper(II) oxide nanoparticles (CuO NPs, mean diameter of 28nm) in water samples was fully investigated. Factors such as Triton X-114 (TX-114) concentration, pH, incubation temperature and time, were optimized. The effects of CuO NP behavior like agglomeration, dissolution, and surface adsorption of natural organic matter, Cu2+, and coating chemicals, on its recovery were studied. The results indicated that all the CPE factors had significant effects on the extraction efficiency. An enrichment factor of ~89 was obtained under optimum CPE conditions. The hydrodynamic diameter of CuO NPs increased to 4-5μm upon agglomeration of NP-micelle assemblies, and decreased at pH >10.0 at which the extraction efficiency was also lowered. The solubility and therefore, the loss of NPs were greatly enhanced at pH 5mgCL-1 and Cu2+ >2 times that of CuO NPs, lowered and enhanced the extraction efficiency, respectively. Pre-treatment of samples with 3% wv-1 of hydrogen peroxide and 10mM of ethylenediaminetetraacetic acid minimized the interferences posed by DOC and Cu2+, respectively. The decrease in CPE efficiency was also evident for ligands like poly(ethylene glycol). The TX-114-rich phase could be determined with either inductively coupled plasma mass spectrometry following microwave digestion, or graphite furnace atomic absorption spectrometry. The detection limits for CuO NPs were 0.02 and 0.06μgL-1 using these techniques, respectively. The optimum sample pre-treatment and CPE conditions were successfully applied to the river and wastewater samples. The relative recoveries of CuO NPs spiked at 5-100μgL-1 (as Cu) in these samples were in the range of between 59.2 and 108.2%. The approach demonstrates a robust analytical method for detecting trace levels of CuO NPs at their original states and assessing their exposure risks in real aquatic environments. © 2014 Elsevier B.V.
Source Title: Analytica Chimica Acta
URI: http://scholarbank.nus.edu.sg/handle/10635/90964
ISSN: 00032670
DOI: 10.1016/j.aca.2014.01.022
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