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A ternary deep eutectic solvent-modified magnetic mixed iron hydroxide@MIL-101(Cr)-NH(2) composite as a sorbent in magnetic solid phase extraction of organochlorine pesticides prior to GC-MS

A green solvent of ternary deep eutectic solvent (menthol-thymol-dodecanoic acid) was prepared and used as a functional reagent to modify a magnetic mixed iron hydroxide@MIL-101(Cr)-NH(2) composite. The proposed sorbent (MIH@MIL-101(Cr)-NH(2)-TDES) was applied in magnetic solid phase extraction (MSP...

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Detalles Bibliográficos
Autores principales: Phosiri, Preeyaporn, Pongpinyo, Prachathipat, Santaladchaiyakit, Yanawath, Burakham, Rodjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018794/
https://www.ncbi.nlm.nih.gov/pubmed/36936839
http://dx.doi.org/10.1039/d2ra07704c
Descripción
Sumario:A green solvent of ternary deep eutectic solvent (menthol-thymol-dodecanoic acid) was prepared and used as a functional reagent to modify a magnetic mixed iron hydroxide@MIL-101(Cr)-NH(2) composite. The proposed sorbent (MIH@MIL-101(Cr)-NH(2)-TDES) was applied in magnetic solid phase extraction (MSPE) for the enrichment of organochlorine pesticides. The analytes were quantitively analyzed by GC-MS. The relationships of experimental parameters for preparing the proposed sorbent and the MSPE method were studied through a Box–Behnken design and a central composite design, respectively. Their optimized conditions were investigated using response surface methodology. Application of the MIH@MIL-101(Cr)-NH(2)-TDES sorbent in MSPE successfully enhanced the sensitivity of GC-MS analysis, giving enrichment factors in the range of 56–168. The MSPE/GC-MS method was developed using MIH@MIL-101(Cr)-NH(2)-TDES as a sorbent and was successfully employed for the preconcentration/determination of organochlorine residues in honey and tea samples. The satisfactory detection limits were in the ranges of 0.07–0.80 ng g(−1) and 0.7–8.5 ng g(−1) for honey and tea samples, respectively. Acceptable recoveries were obtained in the ranges of 81.7–107.3% and 85.4–109.3% for the spiked honey and tea samples, respectively, with RSDs lower than 10.0%.