Volume 68, Issue 11 pp. 2202-2210
ARTICLE

Response surface methodology optimization of supramolecular dispersive liquid-liquid microextraction-solidified floating organic drop of brilliant green and its spectrophotometric determination

Mohammad Bahrami

Mohammad Bahrami

Department of Chemistry, Faculty of Science, Yazd University, Yazd, Iran

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Ali Mohammad Haji Shabani

Corresponding Author

Ali Mohammad Haji Shabani

Department of Chemistry, Faculty of Science, Yazd University, Yazd, Iran

Correspondence

Ali Mohammad Haji Shabani and Shayessteh Dadfarnia, Department of Chemistry, Faculty of Science, Yazd University, 89195-741, Yazd, Iran.

Email: [email protected] (A. M. H) and Email: [email protected] (S. D).

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Shayessteh Dadfarnia

Corresponding Author

Shayessteh Dadfarnia

Department of Chemistry, Faculty of Science, Yazd University, Yazd, Iran

Correspondence

Ali Mohammad Haji Shabani and Shayessteh Dadfarnia, Department of Chemistry, Faculty of Science, Yazd University, 89195-741, Yazd, Iran.

Email: [email protected] (A. M. H) and Email: [email protected] (S. D).

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Mohamad Reza Samadzadeh Yazdi

Mohamad Reza Samadzadeh Yazdi

Department of Mining & Metallurgical Engineering, Yazd University, Yazd, Iran

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First published: 12 September 2021
Citations: 2

Abstract

A simple supramolecular dispersive liquid-liquid microextraction-solidified floating organic drop (SMDLLME-SFOD) method was developed for the separation and preconcentration of brilliant green (BG) before its spectrophotometric determination. The method is based on the extraction of ion-pair of BG with sodium dodecyl sulfate into the coacervates made up of decanoic acid reverse micelles in the tetrahydrofuran-water mixture. The influence of the effective parameters on the extraction of BG was investigated and optimized using response surface methodology. Under the optimized conditions, the calibration graph was linear in the range of 1.0–50.0 μg L−1 of BG. The limit of detection (LOD) and limit of quantification (LOQ) were 0.28 μg L−1 and 0.94 μg L−1, respectively. The repeatability expressed as the relative standard deviation for six replicate measurements at 5.0 μg L−1 BG was 3.6%. The method was successfully applied to the extraction and determination of BG in different water and fish samples.

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