Dispersive magnetic solid‐phase extraction of phthalate esters from water samples and human plasma based on a nanosorbent composed of MIL‐101(Cr) metal–organic framework and magnetite nanoparticles before their determination by GC–MS. Issue 4 (30th January 2018)

• Record Type: Journal Article
• Authors: Dargahi, Rosa; Ebrahimzadeh, Homeira; Asgharinezhad, Ali Akbar; Hashemzadeh, Alireza; Amini, Mostafa M.
• Is Part Of: Journal of separation science. Volume 41:Issue 4(2018)
• Page Start: 948
• Page End: 957
• Publication Date: 2018-01-30
• Subjects: dispersive magnetic solid‐phase extraction -- magnetite nanoparticles -- metal‐organic frameworks -- phthalate esters; Separation (Technology) -- Periodicals; Chromatographic analysis -- Periodicals; 543.089
• DOI: 10.1002/jssc.201700700
• Languages: English
• ISSNs: 1615-9306

Abstract

Abstract: In this study, a magnetic metal–organic framework was synthesized simply and utilized in the dispersive magnetic solid‐phase extraction of five phthalate esters followed by their determination by gas chromatography with mass spectrometry. First, MIL‐101(Cr) was prepared hydrothermally in water medium without using highly corrosive hydrofluoric acid, utilizing an autoclave oven heat supply. Afterward, Fe3 O4 nanoparticles were decorated into the matrix of MIL‐101(Cr) to fabricate magnetic MIL‐101 nanocomposite. The nanocomposite was characterized by various techniques. The parameters affecting dispersive magnetic solid‐phase extraction efficiency were optimized and obtained as: a sorbent amount of 15 mg; a sorption time of 20 min; an elution time of 5 min; NaCl concentration, 10% w/v; type and volume of the eluent 1 mL n ‐hexane/acetone (1:1 v/v). Under the optimum conditions detection limits and linear dynamic ranges were achieved in the range of 0.08–0.15 and 0.5–200 μg/L, respectively. The intra‐ and interday RSD% values were obtained in the range of 2.5–9.5 and 4.6–10.4, respectively. Ultimately, the applicability of the method was successfully confirmed by the extraction and determination of the model analytes in water samples, and human plasma in the range of microgram per liter and satisfactory results were obtained.