On-line electrochemically controlled in-tube solid phase microextraction of inorganic selenium followed by hydride generation atomic absorption spectrometry
Creators
- 1. Department of Chemistry, Tarbiat Modares University, P.O. Box 14115-175, Tehran (Iran, Islamic Republic of)
- 2. Department of Analytical Chemistry, Faculty of Chemistry, K.N. Toosi University of Technology, Tehran (Iran, Islamic Republic of)
Description
In this work, for the first time, a rapid, simple and sensitive microextraction procedure is demonstrated for the matrix separation, preconcentration and determination of inorganic selenium species in water samples using an electrochemically controlled in-tube solid phase microextraction (EC-in-tube SPME) followed by hydride generation atomic absorption spectrometry (HG-AAS). In this approach, in which EC-in-tube SPME and HG-AAS system were combined, the total analysis time, was decreased and the accuracy, repeatability and sensitivity were increased. In addition, to increases extraction efficiency, a novel nanostructured composite coating consisting of polypyrrole (PPy) doped with ethyleneglycol dimethacrylate (EGDMA) was prepared on the inner surface of a stainless-steel tube by a facile electrodeposition method. To evaluate the offered setup and the new PPy-EGDMA coating, it was used to extract inorganic selenium species in water samples. Extraction of inorganic selenium species was carried out by applying a positive potential through the inner surface of coated in-tube under flow conditions. Under the optimized conditions, selenium was detected in amounts as small as 4.0 parts per trillion. The method showed good linearity in the range of 0.012–200 ng mL−1, with coefficients of determination better than 0.9996. The intra- and inter-assay precisions (RSD%, n = 5) were in the range of 2.0–2.5% and 2.7–3.2%, respectively. The validated method was successfully applied for the analysis of inorganic selenium species in some water samples and satisfactory results were obtained. - Graphical abstract: An electrochemically controlled in-tube solid phase microextraction followed by hydride generation atomic absorption spectrometry was developed for extraction and determination ultra-trace amounts of Se in aqueous solutions. - Highlights: • A nanostructured composite coating consisting of PPy doped with EGDMA was prepared. • The coating was synthesised electrochemically in inner surface of a stainless-steel capillary tube. • It was used to extract Se from water samples followed by hydride generation AAS. • Extraction of selenium was carried out by applying a positive potential into in-tube SPME. • Ultra trace amounts of Se with LOD = 8.0 ppt was detected in aqueous solutions.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.aca.2016.04.001Additional details
Identifiers
- DOI
- 10.1016/j.aca.2016.04.001;
- PII
- S0003-2670(16)30423-8;
Publishing Information
- Journal Title
- Analytica Chimica Acta
- Journal Volume
- 922
- Journal Page Range
- p. 37-47
- ISSN
- 0003-2670
- CODEN
- ACACAM
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48002235
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ABSORPTION SPECTROSCOPY; AQUEOUS SOLUTIONS; ATOMIZATION; DOPED MATERIALS; ELECTROCHEMISTRY; ELECTRODEPOSITION; EXTRACTION; HYDRIDES; NANOSTRUCTURES; ORGANIC POLYMERS; PYRROLES; SELENIUM; STAINLESS STEELS; SYNTHESIS; TRACE AMOUNTS
- Descriptors DEC
- ALLOYS; AZOLES; CARBON ADDITIONS; CHEMISTRY; DEPOSITION; DISPERSIONS; ELECTROLYSIS; ELEMENTS; HETEROCYCLIC COMPOUNDS; HIGH ALLOY STEELS; HOMOGENEOUS MIXTURES; HYDROGEN COMPOUNDS; IRON ALLOYS; IRON BASE ALLOYS; LYSIS; MATERIALS; MIXTURES; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; POLYMERS; SEMIMETALS; SEPARATION PROCESSES; SOLUTIONS; SPECTROSCOPY; STEELS; SURFACE COATING; TRANSITION ELEMENT ALLOYS
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.