A centrifuge-less cloud point extraction-spectrophotometric determination of copper(II) using 6-hexyl-4-(2-thiazolylazo)resorcinol
[Display omitted] •A new cloud point extraction-chromogenic system for Cu(II) was studied.•A novel commercially available hydrophobic thiazolylazo dye was used.•The developed procedure is simple, sensitive, economical, and green.•Water samples and a saline solution for infusion were analyzed for Cu(...
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Published in: | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Vol. 262; p. 120106 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier B.V
05-12-2021
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Subjects: | |
Online Access: | Get full text |
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Summary: | [Display omitted]
•A new cloud point extraction-chromogenic system for Cu(II) was studied.•A novel commercially available hydrophobic thiazolylazo dye was used.•The developed procedure is simple, sensitive, economical, and green.•Water samples and a saline solution for infusion were analyzed for Cu(II).
A simple, cheap, and environmentally friendly centrifuge-less cloud point extraction procedure was developed for the preconcentration of traces of Cu(II) before its spectrophotometric determination. It is based on a complexation reaction with the hydrophobic azo reagent 6-hexyl-4-(2-thiazolylazo)resorcinol (HTAR), in which a complex with a stoichiometric ratio of 1:1 and an absorption maximum at 535 nm is formed. The experimental conditions for Cu(II) determination were found: HTAR concentration (8 × 10−6 mol mL−1), mass fraction of the surfactant Triton X-114 (2.2%), pH (5.9, ammonium acetate buffer), and incubation time (10 min at 60 °C). The linear range, limit of detection, molar absorption coefficient and preconcentration factor were calculated to be 4.5–254 ng mL−1, 1.34 ng mL−1, 2.54 × 105 L mol−1 cm−1, and 10, respectively. The effect of foreign ions was studied, and the proposed procedure was applied to the analysis of water samples and a saline solution for intravenous infusion. |
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ISSN: | 1386-1425 |
DOI: | 10.1016/j.saa.2021.120106 |