Dispersive liquid-liquid microextraction followed by high-performance liquid chromatography-diode array detection as an efficient and sensitive technique for determination of antioxidants
(2007) In Analytica Chimica Acta 591(1). p.69-79- Abstract
- Dispersive liquid-liquid microextraction (DLLME) and high performance liquid chromatography-diode array detection (HPLC-DAD) was presented for extraction and determination of Irganox 1010, Irganox 1076 and Irgafos 168 (antioxidants) in aqueous samples. Carbon tetrachloride at microliter volume level and acetonitrile were used as extraction and dispersive solvents, respectively. The main advantages of method are high speed, high enrichment factor, high recovery, good repeatability and extraction solvent volume at mu L level. Limit of detection for analytes is between 3 and 7 ng mL(-1). One variable at a time optimization and response surface modeling were used to obtain optimum conditions for microextraction procedure and nearly same... (More)
- Dispersive liquid-liquid microextraction (DLLME) and high performance liquid chromatography-diode array detection (HPLC-DAD) was presented for extraction and determination of Irganox 1010, Irganox 1076 and Irgafos 168 (antioxidants) in aqueous samples. Carbon tetrachloride at microliter volume level and acetonitrile were used as extraction and dispersive solvents, respectively. The main advantages of method are high speed, high enrichment factor, high recovery, good repeatability and extraction solvent volume at mu L level. Limit of detection for analytes is between 3 and 7 ng mL(-1). One variable at a time optimization and response surface modeling were used to obtain optimum conditions for microextraction procedure and nearly same experimental conditions were obtained using both optimization methods. Recoveries in the ranges 78-86% and 84-110% were obtained by one variable at a time and response surface modeling, respectively. Using tap water and packed water as matrices do not show any detrimental effect on the extraction recoveries and enrichment factors of analytes. (C) 2007 Elsevier B.V. All rights reserved. (Less)
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https://lup.lub.lu.se/record/659728
- author
- Farajzadeh, Mir Ali ; Bahram, Morteza and Jönsson, Jan Åke LU
- organization
- publishing date
- 2007
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- one variable at a time, sample preparation, liquid chromatography, high-performance, dispersive liquid-liquid extraction, antioxidant, optimization, response surface modeling
- in
- Analytica Chimica Acta
- volume
- 591
- issue
- 1
- pages
- 69 - 79
- publisher
- Elsevier
- external identifiers
-
- wos:000246498900011
- scopus:34247156770
- ISSN
- 1873-4324
- DOI
- 10.1016/j.aca.2007.03.040
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Analytical Chemistry (S/LTH) (011001004)
- id
- 1af8042a-e5b0-4c70-bd88-3b2fa00fd07e (old id 659728)
- date added to LUP
- 2016-04-01 16:23:46
- date last changed
- 2022-04-22 21:41:08
@article{1af8042a-e5b0-4c70-bd88-3b2fa00fd07e,
abstract = {{Dispersive liquid-liquid microextraction (DLLME) and high performance liquid chromatography-diode array detection (HPLC-DAD) was presented for extraction and determination of Irganox 1010, Irganox 1076 and Irgafos 168 (antioxidants) in aqueous samples. Carbon tetrachloride at microliter volume level and acetonitrile were used as extraction and dispersive solvents, respectively. The main advantages of method are high speed, high enrichment factor, high recovery, good repeatability and extraction solvent volume at mu L level. Limit of detection for analytes is between 3 and 7 ng mL(-1). One variable at a time optimization and response surface modeling were used to obtain optimum conditions for microextraction procedure and nearly same experimental conditions were obtained using both optimization methods. Recoveries in the ranges 78-86% and 84-110% were obtained by one variable at a time and response surface modeling, respectively. Using tap water and packed water as matrices do not show any detrimental effect on the extraction recoveries and enrichment factors of analytes. (C) 2007 Elsevier B.V. All rights reserved.}},
author = {{Farajzadeh, Mir Ali and Bahram, Morteza and Jönsson, Jan Åke}},
issn = {{1873-4324}},
keywords = {{one variable at a time; sample preparation; liquid chromatography; high-performance; dispersive liquid-liquid extraction; antioxidant; optimization; response surface modeling}},
language = {{eng}},
number = {{1}},
pages = {{69--79}},
publisher = {{Elsevier}},
series = {{Analytica Chimica Acta}},
title = {{Dispersive liquid-liquid microextraction followed by high-performance liquid chromatography-diode array detection as an efficient and sensitive technique for determination of antioxidants}},
url = {{http://dx.doi.org/10.1016/j.aca.2007.03.040}},
doi = {{10.1016/j.aca.2007.03.040}},
volume = {{591}},
year = {{2007}},
}