Combination of graphene oxide-based solid phase extraction and electro membrane extraction for the preconcentration of chlorophenoxy acid herbicides in environmental samples
| Autor: | Mohammad Behbahani, Hadi Tabani, Akbar Bagheri, Abolfath Shahsavani, Ali Reza Fakhari, Saeed Nojavan, Mani Salarian |
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| Rok vydání: | 2013 |
| Předmět: |
Biochemistry
Phenoxyacetates Analytical Chemistry chemistry.chemical_compound Acetic acid Capillary electrophoresis Rivers Sample preparation Solid phase extraction Aqueous solution Chromatography Chemistry Elution Herbicides Organic Chemistry Solid Phase Extraction Electrophoresis Capillary Reproducibility of Results Membranes Artificial General Medicine 1-Octanol Hydrogen-Ion Concentration Propanoic acid Distilled water Research Design Graphite Water Pollutants Chemical |
| Zdroj: | Journal of chromatography. A. 1300 |
| ISSN: | 1873-3778 |
| Popis: | Combination of different extraction methods is an interesting and debatable work in the field of sample preparation. In the current study, for the first time, solid phase extraction combined with electro membrane extraction (SPE–EME) was developed for ultra-preconcentration and determination of chlorophenoxy acid herbicides in environmental samples using capillary electrophoresis (CE). In the mentioned method, first, a 100 mL of chlorophenoxy acid herbicides (2-methyl-4-chlorophenoxyacetic acid (MCPA), 2-(2,4-dichlorophenoxy) propanoic acid (2,4-DP) and 2-(4-chloro-2-methylphenoxy) propanoic acid (MCPP)) was passed through a column of graphene oxide as a solid phase, and then the adsorbed herbicides were eluted by 4.0 mL of 8% acetic acid (HOAC) in methanol. Then, the elution solvent was evaporated and the herbicides residue was dissolved in 4.0 mL of double distilled water (pH 9.0). Afterwards, the herbicides in 4.0 mL of the aqueous solution were transferred to an EME glass vial. In the EME step, the herbicides were extracted from the sample solution into the basic acceptor solution (pH 13.0) under electrical potential, which was held inside the lumen of the fiber with 1-octanol as the supported liquid membrane (SLM). Under the optimized conditions, high enrichment factors were obtained in the range of 1950–2000. The limits of quantification (LOQs) and method detection limits (MDLs) were obtained in the range of 1.0–1.5 and 0.3–0.5 ng mL −1 , respectively. Finally, the performance of the present method was evaluated for extraction and determination of chlorophenoxy acid herbicides in environmental samples. |
| Databáze: | OpenAIRE |
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