4.6 Article

Keggin type phosphotungstic acid intercalated copper-chromium-layered double hydroxide reinforced porous hollow fiber as a sorbent for hollow fiber solid phase microextraction of selected chlorophenols besides their quantification via high performance liquid chromatography

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1697, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.chroma.2023.463993

Keywords

Layered double hydroxide; Keggin-type polyoxometalate; Chlorophenols; Hollow fiber solid phase microextraction

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A copper-chromium-layered double hydroxide (Cu/Cr-LDH) was synthesized by the co-precipitation method and intercalated with Keggin-type polyoxometalate (H3PW12O40). The modified LDH was used for the extraction of chlorophenols from water and tea samples using the HF-solid phase microextraction method (HF-SPME). The method showed good performance with high enrichment factors and accurate quantification of the target analytes.
Herein, a copper-chromium-layered double hydroxide (Cu/Cr-LDH) was synthesized by the co -precipitation method. The Cu/Cr-LDH was intercalated to the Keggin-type polyoxometalate (H3PW12O40). The modified LDH accommodated in the pores of hollow fiber (HF), to prepare the extracting device for the HF-solid phase microextraction method (HF-SPME). The method was used for the extraction of 4-chlorophenol, 2,4-dichlorophenol, and 2,4,6-trichlorophenol from tap water, river water, and tea sample. The extracted target analytes were quantified via high-performance liquid chromatography-UV detection. The figures of merit of the method such as, linear dynamic ranges (LDRs), limit of detections (LODs) and, limit of quantifications (LOQs), were determined based on the obtained optimum condition. Based on the results, the LDR was between 1 and 500 mu g L - 1 and r 2 higher than 0.9960. The LODs and LOQs were obtained in the ranges of 0.28-0.36 mu g L - 1 and 0.92-1.1 mu g L - 1 , respectively. The relative standard deviations ((RSDs% for inter-and intra-day) of the method for the extraction of target analytes were cal-culated in two different concentrations of (2 and 10 mu g L - 1 ) and (5 and 10 mu g L - 1 ) between 3.70% -5.30% and 3.50% -5.70%-respectively. The enrichment factors were obtained between 57 and 61. In order to investigate the accuracy of the method, also the relative recovery was obtained, between 93 and 105%. Finally, the proposed method was used for the extraction of the selected analytes in different water and tea samples.(c) 2023 Elsevier B.V. All rights reserved.

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