Preparation of a New Solid-Phase Microextraction Fiber by Coating Silylated Nanoporous Silica on a Copper Wire (original) (raw)
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Analytica Chimica Acta, 2009
Nanoporous silica (SBA-15) was prepared and functionalized with 3-[Bis(2-hydroxyethyl)amino] propyl-triethoxysilane (HPTES) to be used as a highly porous fiber coating material for solid-phase microextraction (SPME). The prepared HPTES-SBA-15 particles had a lengthy morphology and a specific surface area of 790 m 2 g −1 . They were characterized by N 2 sorption analyses, scanning electron microscopy and thermogravimetric analysis. The prepared nanomaterial was immobilized onto a copper wire for fabrication of the SPME fiber. The fiber was evaluated for the extraction of BTEX and some phenolic compounds in combination with GC-MS. For optimization of factors affecting the extraction efficiency of the phenolic compounds, a simplex optimization method was used. The proposed fiber showed some selectivity towards the polar phenolic compounds with extraction efficiencies better than a PDMS commercial fiber. The repeatability for one fiber (n = 5), expressed as relative standard deviation (RSD), was between 6.5% and 9.8% and the reproducibility for five prepared fibers was between 8.2% and 11.3% for the test compounds. No significant change was observed in the extraction efficiency of the new SPME fiber over 50 extractions. The fiber was successfully applied to the determination of phenolic compounds in spiked river water and sewage samples. Thus, HPTES-SBA-15 fiber is a promising alternative to the commercial fibers as it is robust, selective, highly porous and easily and inexpensively prepared.
Inorganic/organic mesoporous silica as a novel fiber coating of solid-phase microextraction
Talanta, 2004
Mesoporous materials were employed as fast, sensitive and efficient fiber coatings of solid-phase microextraction (SPME) for the first time. Three micrometer as-synthesized C(16)-MCM-41 particles were immobilized onto stainless steel wire with 100mum coating thickness. In combination with high performance liquid chromatography (HPLC), extraction efficiency and selectivity of C(16)-MCM-41 were investigated using aromatic hydrocarbons. Effect of extraction and desorption time, extraction temperature, stirring rate and ionic strength on extraction efficiency were examined. Aanalytical merits of SPME with C(16)-MCM-41 coating were evaluated. The chromatographic peak area is proportional to the concentration of anthracene in the range 0.5-150mugl(-1). The limit of detection was 0.05mugl(-1) (S/N=3) and the relative standard deviation (R.S.D.) was 0.033%.
Journal of chromatography. A, 2015
In the present study, 12-tungstophosphoric (PW) acid as heteropoly acid, supported on silica-coated γ-Fe2O3 nanoparticles (NPs), was used as a new fiber coating for solid-phase microextraction (SPME). The γ-Fe2O3@SiO2-PW nanocomposite with high surface area was synthesized and characterized by SEM and FT-IR. The prepared nanocomposite was immobilized on a stainless steel wire for fabrication of the SPME fiber. The fiber was evaluated for the extraction of some phenolic compounds (PCs) from water sample in combination with gas chromatography-mass spectrometry (GC-MS). A one-at-a-time optimization strategy was applied for optimizing the important extraction parameters such as extraction temperature, extraction time, ionic strength, stirring rate, pH, and desorption temperature and time. In optimum conditions, the repeatability for one fiber (n=3), expressed as relative standard deviation (R.S.D. %), was between 4.8% and 9.6% for the test compounds. The detection limits for the studied...
Journal of Chromatographic Science, 2002
In this study, solid-phase microextraction fibers coated with modified silica particles (5 µm dp) bonded to methyl (C 1 ), hexyl (C 6 ), octyl (C 8 ), and polymeric octadecyl (C 18 ) groups are prepared and evaluated. Selective extraction of polycyclic aromatic hydrocarbons (PAHs) from river water is used to demonstrate the selective behavior of the fibers as a function of the alkyl chains bonded to the silica phase. Scanning electron micrography suggests that the coating structure consists in a monolayer of particles bonded to the surface of the fiber. The behavior of the fibers upon the extraction of PAHs from water samples is compared with the use of standard polydimethylsiloxane fibers that are commercially available.
Analytica Chimica Acta, 2005
An aniline-based polymer was electrochemically prepared and applied as a new fiber coating for solid phase microextraction (SPME) of some priority phenols from water samples. The polyaniline (PANI) film was directly electrodeposited on the platinum wire surface in sulfuric acid solution using cyclic voltammetry (CV) technique. The efficiency of new coating was investigated using a laboratory-made SPME device and gas chromatography with flame ionization detection for the extraction of some phenols from the headspace of aqueous samples. The scanning electron microscopy (SEM) images showed the homogeneity and the porous surface structure of the film. The results obtained proved the ability of this polymer as a suitable SPME fiber coating for trapping the selected phenols. Influential parameters affecting the extraction process were optimized and an extraction time of 50 min at 50 • C gave maximum efficiency, when the aqueous sample was saturated with NaCl and adjusted at pH 2. This new coating can be prepared easily in a reproducible manner and it is rather inexpensive and stable against most of organic solvents. The PANI thickness can be precisely controlled by the number of CV cycles. At the optimum conditions, the R.S.D. for a double distilled water spiked with phenol and chlorophenols at ppb level were 4.8-17% (n = 3) and detection limits for the studied compounds were between 0.69 and 3.7 ng ml −1 , except for phenol and 4-chlorophenol. The optimized method was successfully applied to some real-life water samples.
Analytica Chimica Acta, 2007
A new fiber for solid-phase microextraction (SPME) employing a metallic support coated with an inorganic material is proposed. A nitinol alloy (NiTi) was used as the support material due to its super elasticity and shape memory properties. Zirconium oxide (ZrO 2) was electrodeposited onto NiTi using chronoamperometry. The surface characteristics and morphology of the coated and uncoated support were evaluated through scanning electronic microscopy and dispersive energy microanalysis. This assembly was applied in the extraction of three halophenols from aqueous samples. A multivariate approach was used for optimization of the variables involved in the system. The Doehlert matrix was used for evaluation of the best derivatization conditions and a Box-Behnken design to obtain the best extraction conditions. In order to investigate the repeatability, one fiber was used for six extraction tests under similar conditions and the relative standard deviations (R.S.D.) were lower than 12.5%. Detection limits were lower than 0.30 ng mL −1. Correlation coefficients were higher than 0.997. Extraction efficiency of the NiTi-ZrO 2 fiber was similar to a PDMS 7 m commercial fiber, even though it had a lower coating thickness of 1.35 m. Considering the amount extracted per unit volume, the NiTi-ZrO 2 fiber had a better extraction profile when compared to commercial fibers. The new SPME fiber has a lifetime of over 500 extractions. Thus, it is a promising alternative for low-cost analysis, as the proposed fiber is robust, and easily and inexpensively prepared.
Journal of separation science, 2015
In this research, a carbon nanotube/layered double hydroxide nanocomposite was synthesized by an in situ growth route by electrostatic force. The prepared carbon nanotube/layered double hydroxide nanocomposite was successfully prepared and deposited on a stainless-steel wire for the fabrication of the solid-phase microextraction fiber. The fiber was evaluated for the extraction of phenolic compounds from water samples. Analytical merits of the method, under optimum conditions (extraction temperature: 75°C, extraction time: 30 min, desorption time: 2 min, desorption temperature 260°C, salt concentration: 10% w/v) are 0.01-300 ng/mL for the linear dynamic range and 0.005-0.08 for the limit of detection. In optimum conditions, the repeatability for one fiber (n = 3), expressed as relative standard deviation, was between 6.5 and 9.9% for the phenolic compounds.
Novel unbreakable solid-phase microextraction fiber by electrodeposition of silica sol-gel on gold
Journal of Separation Science, 2011
A new technique for preparation of an unbreakable solid-phase microextraction (SPME) fiber, using sol-gel technology is developed. Primarily, an ultrathin two-dimensional intermediate film was prepared by hydrolysis of 3-(trimethoxysilyl)-1-propanthiol selfassembled monolayer grafted onto gold, then a stationary phase by electrodeposition of 3-(trimethoxysilyl)propylmethacrylate as a precursor, tetramethyl orthosilicate and polyethylene glycol as a coating polymer was produced. The scanning electron microscopy images revealed that the new fiber exhibits a rather porous and homogenous surface. The thermal stability of the fabricated fiber was investigated by thermogravimetric analysis. The applicability of the prepared fiber coating in conjunction with gas chromatographymass spectrometry was examined by SPME of polycyclic aromatic hydrocarbons, as model analytes, from aquatic media. An extraction time of 20 min at 501C gave maximum peak areas when NaCl, 15% was added to the aqueous samples. Limits of detection were in the range of 0.01-0.02 ng/mL and relative standard deviation values were in the range of 4-16% at 1 ng/mL. The developed method was successfully applied for the analysis of real water samples while the relative recovery percentage was in the range of 102-118%.