Abstract
A novel method for the spectrophotometric determination of trace amounts of molybdenum has been developed. This method utilizes a centrifuge-less cloud point extraction (CL-CPE) in a mixed micellar (MM) system containing a nonionic surfactant (Triton X-114) and an ionic liquid (Aliquat® 336, A336). The chromophore chelating reagent employed was 4-nitrocatechol (4NC, H2L). This work marks its first application as a CPE reagent. Under the optimal conditions, Mo(VI) forms a yellow ternary complex with 4NC and A336, which can be represented by the formula (A336+)2[MoO2L2]. The method possesses the following characteristics: limit of detection (LOD) of 3.2 ng mL−1, linear range of 10.8–580 ng/mL, absorption maximum of 435 nm, molar absorptivity coefficient of 3.34 × 105 L mol−1 cm−1, and Sandell’s sensitivity of 0.29 ng cm−2. The method has been successfully employed for the determination of molybdenum in reference standard steel samples, bottled mineral water, and a molybdenum-containing dietary supplement.
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Divarova, V., Gajdošová, A., Racheva, P., & Gavazov, K. (2025). An Ionic Liquid-Assisted Mixed Micelle-Mediated Centrifuge-Less Cloud Point Extraction Spectrophotometric Method for the Determination of Molybdenum(VI). International Journal of Molecular Sciences, 26(10). https://doi.org/10.3390/ijms26104597
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