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Prof. Sivanesan Subramanian

Anna University, India

 

Prof. Hassan Karimi-Maleh

University of Electronic Science
and Technology of China (UESTC)

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Home > Archives > Vol. 8 No. 2(Published) > Original Research Article
ACE-5603

Published

2025-05-19

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Vol. 8 No. 2(Published)

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Original Research Article

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Copyright (c) 2025 Zianab Tariq, Alaa S. Alwan, Layth S. Jasim

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How to Cite

Tariq, Z., S. Alwan, A., & S. Jasim, L. (2025). Application of central composite design and desirability function in the optimization of spectrophotometric method for quantification of fast green FCF using a green microextraction method. Applied Chemical Engineering, 8(2), ACE-5603. https://doi.org/10.59429/ace.v8i2.5603
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Application of central composite design and desirability function in the optimization of spectrophotometric method for quantification of fast green FCF using a green microextraction method

Zianab Tariq

Department of Chemistry, College of Sciences, University of Al-Qadisiyah, Dewanyia, 58002, Iraq

Alaa S. Alwan

Department of Chemistry, College of Sciences, University of Al-Qadisiyah, Dewanyia, 58002, Iraq

Layth S. Jasim

Department of Chemistry, College of Education, University of Al-Qadisiyah, Diwaniyah, 58002, Iraq


DOI: https://doi.org/10.59429/ace.v8i2.5603


Keywords: SHS-LPME: switchable hydrophilicity solvent liquid phase microextraction, FG: Fast green FCF and df: degree of freedom


Abstract

The aim of this article is to develop a "switchable hydrophilicity solvent liquid phase microextraction" (SHS-LPME) for the effectual extraction of fast green FCF. Three "switchable hydrophilicity solvents" (SHSs) were practiced for the extraction of fast green FCF. The attained extract phase afterward phase separation was evaluated by UV-VIS spectrophotometry. The extraction parameters such as, SHS volume, HNO3 volume and NaOH volume, were enhanced using central composite design and desirability function. Under optimized conditions, the linear range 0.50-5.00 µg/ mL with R2 = 0.9886, limit of detection 0.341 µg/ mL, limit of quantitation 1.026 µg/ mL. The method showed a relative standard deviation (RSD) of 1.16% for 7 replicate measurements. Preconcentration and Enrichment factors were determined to be 20 and 35 respectively, indicating the method’s efficiency in enhancing fast green detection. The proposed method was applied in real samples successfully.


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