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1.
A new method for the determination of butyltin species by ion-exchange chromatography linked with graphite-furnace electrothermal atomic absorption spectrometry (ETAAS) is presented. The separation is achieved on a strong cation-exchange column with a 0.18 mol dm?3 solution of diammonium citrate at pH 6.5 with a step change to pH 4.0 in 60:40 methanol/water solvent. ETAAS detection is performed on-line using an oxidizing matrix modifier. Mono-, di- and tri-butyltin may be determined in a single experiment with detection limits of (respectively) 0.5, 1.1 and 0.8 ng (Sn). Applications to actual samples are reported. 相似文献
2.
Centineo G Rodríguez-González P Blanco González E García Alonso JI Sanz-Medel A Font Cardona N Aranda Mares JL Ballester Nebot S 《Analytical and bioanalytical chemistry》2006,384(4):908-914
A standard GC-MS instrument with electron impact ionisation has been used to develop a fast, simple and reliable method for
the simultaneous determination of monobutyltin (MBT), dibutyltin (DBT) and tributyltin (TBT) in water samples. Isotope dilution
analysis (IDA) is used for the determination of species, taking advantage of a commercially available spike solution containing
a mixture of MBT, DBT and TBT enriched in 119Sn. Method detection limits for 100-mL samples were between 0.18 and 0.25 ng L−1 for the three butyltin compounds with typical RSD between 2 and 4% at levels between 100 and 10 ng L−1, respectively. Recovery of tin species in spiked samples (natural water, wastewater and seawater) was quantitative. The stability
of butyltin compounds in collected seawater samples was also studied. The addition of a 1% (v/v) glacial acetic acid preserved
tin species in the samples for at least 5 days at room temperature. The IDA method was finally implemented in a routine testing
laboratory and it was subsequently accredited by the Spanish National Accreditation Body according to the requirements of
UNE-EN ISO/IEC 17025. 相似文献
3.
There have been many methods available for the determination of butyltin compounds in sediment. The variations of these methods are not in the methods of determination but rather in the extraction of these compounds from the complex matrices. All of these methods have not been critically compared or evaluated, mainly because of the lack of a suitable reference sediment for butyltin compounds. Recently, the National Research Council of Canada has introduced a reference sediment (PACS-1) which contains certified values of butyltin compounds. The present study compares the recoveries of ten extraction techniques for butyltin species using ethylation derivatization and GC AA as the method of determination. Of these ten methods, only four were found satisfactory for extraction of the dibutyltin and tributyltin species. None of the methods evaluated, however, could quantitatively extract monobutyltin from sediment. 相似文献
4.
Speciation of butyltin compounds by liquid chromatography coupled to electrothermal atomic absorption spectrometry of toluene solutions containing tropolone is applied to sediment samples. Tributyltin and dibutyltin may be determined at concentrations as low as a few ng · g–1. Monobutyltin is strongly retained, tetrabutyltin is not separated from tributyltin. 相似文献
5.
A large amount of data has appeared in the literature within the last few years dealing with the monitoring of butyltin compounds in coastal environments. However, the strategies used strongly differed from one author to another, which led to difficulties in the comparison of contamination levels and the evaluation of long-term trends. In this paper, different causes of pitfalls due to uncontrolled sources of variability are addressed; they involve precautions to be undertaken for the monitoring of butylins in water and sediment, particularly: sample collection; sample pretreatment (filtration/centrifugation, acidification, sieving); sample storage (different methods for storage and drying procedures); variability over the same site; variations over a tidal cycle; and variability due to diffusion (e.g. due to flushing). 相似文献
6.
Nil Ozbek 《International journal of environmental analytical chemistry》2016,96(6):505-514
In this work, water and nitric acid extractable sulphur concentrations in PM2.5 fraction of urban aerosols were determined by high-resolution continuum source electrothermal molecular absorption spectrometry using most suitable CS molecular absorption band at 258.056 nm. For this purpose, the PM2.5 airborne particulates were collected on quartz filters using a high-volume sampler (500 L/min) in Istanbul (Turkey) during six months (January–June) of two consecutive years. The instrumental and experimental parameters (pyrolysis temperature, molecule formation temperature and leaching reagents) were optimised. The validity of the method for the sulphur was tested using standard reference material and the results were found to be in the uncertainty limits of the certified value. 相似文献
7.
Nuray Şatıroğlu İlknur Tokgöz 《International journal of environmental analytical chemistry》2013,93(7):560-572
Cloud point extraction was applied as a preconcentration step for the determination of trace level of Al(III) in water samples with electrothermal atomic absorption spectrometry (ETAAS), flame atomic absorption spectrometry (FAAS) and UV-visible spectrophotometry. The aluminum was extracted as aluminum-Eriochrome Cyanine R (ECR) complex, at pH 6 by micelles of the non-ionic surfactant octylphenoxypolyethoxyethanol (Triton X-114). The investigations showed that the same CPE procedure can be used for different detection techniques. The results obtained from these techniques were evaluated. Under the optimal conditions, limit of detection obtained with ETAAS, FAAS and UV-visible spectrophotometry were 0.03 ng mL?1, 0.06 µg mL?1 and 0.01 µg mL?1, respectively. The accuracy of the procedure was tested by analysing certified reference material. The method was successfully applied to determination of aluminum in water samples and dialysis fluid. 相似文献
8.
对海水中甲基、丁基锡的氢化反应与捕集、色谱分离及其原子化等进行了条件实验和最佳化。采用15cmChromosorbGAW—DMCS载体和OV—3固定液,色谱分离锡的无机、一甲、二甲、三甲、一丁、二丁、三丁基化合物的保留时间分别为40、100、125、139、160、191、228s;在0.200dm3水样中直接测定海水中各形态锡的检出限分别为1.9、1.6、1.8、3.0、1.3、1.4、22.4、ngSn·dm-3;其相应的测量精密度在10%左右。 相似文献
9.
Nadica Todorovska Irina Karadjova Sonja Arpadjan Trajce Stafilov 《Central European Journal of Chemistry》2007,5(1):230-238
A simple, accurate and reliable method for direct electrothermal atomic absorption spectrometric (ETAAS) determination of
chromium in serum and urine samples without any preliminary sample pretreatment is described. Instrumental parameters are
optimized in order to define: the most suitable atomizer, optimal temperature program and efficient modifier. An appropriate
quantification method is proposed taking into account a matrix interference study. Pyrocoated graphite tubes and wall atomization,
pretreatment temperature of 700 °C, atomization temperature of 2600 °C, hydrogen peroxide as modifier and standard addition
calibration are recommended. The accuracy of the method proposed for Cr determination in serum and urine was confirmed by
comparative analysis of parallel samples after wet or dry ashing as well as by the analysis of two certified reference materials:
Serum, Clin Rep 1 and Lypochek Urine, level 1. The detection and determination limits achieved for both matrices are 0.08
μg/L and 0.15 μg/L respectively. The relative standard deviation varied between 15 and 18 % for the chromium content in the
samples in the range 0.08–0.2 μg/L and between 4 and 7 % for the chromium content in the range 0.2–2.0 μg/L for both matrices.
相似文献
10.
Carbon nanotubes are a kind of new carbon-based nanomaterials, which have drawn great attention in many application fields. The potential of single-walled carbon nanotubes (SWCNTs) as solid-phase microextraction (SPME) adsorbent for the preconcentration of environmental pollutants has been investigated in recent years. In the present study, the feasibility of SWCNTs as SPME adsorbent for the determination of monobutyltin, dibutyltin and tributyltin in seawater samples was studied. To achieve this aim, the potential factors affecting the SPME efficiency, including extraction time, extraction temperature, desorption time, desorption temperature, and salinity were optimized. The developed method showed good performance according to the ICH (International Conference on Harmonization of Technical Requirements for Analytical Methods) criteria. The acquired calibration curves were linear (r ≥ 0.992) over the concentration range from ≤12 to 2000 ng L−1. For all of the analytes, the limit of detection at signal-to-noise ratio of 3 was below 5 ng L−1. Furthermore, in comparison with the commercial carboxen/polydimethylsiloxane fiber, the developed SWCNT fiber showed better thermal stability (over 350 °C) and longer life span (over 150 times). The application of the proposed method in environmental analyses was shown by analyzing seawater samples from the harbors on the Persian Gulf for butyltin residues. Some of the butyltins were detected in the analyzed samples. Results of the present study demonstrate the feasibility of the SWCNTs as SPME adsorbent for the determination of butyltins in seawater samples. 相似文献
11.
Butyltin compounds are widespread contaminants which have also been found in some wines, determined by liquid-liquid extraction followed by alkylation with a Grignard reagent and gas chromatography-mass spectrometric (GC-MS) analysis. A promising alternative to this extraction/derivatization method is the one-step tetraethylborate in situ ethylation/solid-phase micro-extraction (SPME) method. In this work, a SPME-GC-MS method for the determination of butyltin compounds in wine was optimised. The optimised parameters concerned the pre-treatment with tetramethylammonium hydroxide, matrix modification with sodium chloride, tetraethylborate concentration, extraction time and temperature, and the GC separation program. The analytical figures of merit of the optimised method (range, limit of detection (LOD) and reproducibility) were evaluated. The sensitivity (range 20-1421 kcounts μg−1 l−1 as Sn) and LOD (range, 0.01-0.2 μg l−1 as Sn) depended greatly on the butyltin species to be measured and on the type of wine. For the tested species (monobutyltin, dibutyltin and tributyltin) the highest sensitivities were achieved for Port wine samples, followed by red wine>white wine>white Verde wine. The method allowed acceptable repeatability (relative standard deviation (R.S.D.), 6-8%; n=4) and reproducibility (R.S.D., 8-9%; n=3). 相似文献
12.
Experimental instrumentation for the speciation of butyltin compounds by hydride generation and gas chromatography-quartz furnace atomic absorption spectrometry is described. Evaluation of a number of extraction methods revealed that simple acid leaching of oyster samples gave adequate recoveries. The levels of each butyltin species in oyster flesh and gill are reported together with the tentative identification of a mixed methylbutyltin compound. 相似文献
13.
The optimization and application of gas chromatograph coupled with inductively coupled plasma mass spectrometer (GC-ICPMS) (equipped with a commercially available interface) for the speciation of butyltin compounds in freshwater origin sediment and mussel samples is described. Optimization focused on the system parameters that have the greatest effect on signal intensity such as plasma power, ion lenses and make up gas flow (in the interface). Xenon (Xe) containing argon gas (Ar) was applied as tuning gas providing continuous Xe signal for the optimization of system parameters. It was found that plasma power and make up gas are interrelated variables and provide a set of paired optimum values at each power settings. The absolute optimum values obtained at 800 W plasma power and 1.2 L min−1 make up gas flow rate when 7 mm sample depth was adjusted. The optimum settings obtained were then checked by means of a test solution (tetraethyltin dissolved in hexane). Same optimum conditions were found when tin (Sn) transient signals were monitored. Detection limits were calculated for the three species using the optimized system parameters. Detection limits are the following: for monobutyltin (MBT) 5.6 ng Sn kg−1, for dibutyltin (DBT) 6.6 ng Sn kg−1 and for tributyltin (TBT) 3.4 ng Sn kg−1 obtained. Determination of the butyltin compounds were carried out by means of species-specific isotope dilution analysis. The spike solution contained all species investigated but with altered isotopic composition. Each species were enriched in their 119Sn isotope. Concentrations found in Hungarian freshwater origin mussel and sediment samples ranged between 19 and 39 ng g−1for MBT, between 1.2 and 6.3 ng g−1 for DBT and between 1.2 and 3.2 ng g−1 for TBT indicated as Sn in dry weight. Validation of the method was done by means of certified reference materials (BCR CRM 646 and 477). Good agreement was found between certified and experimental values. Normalized deviation (En) was also computed in order to validate the method used. En values obtained ranged between 0.07 and 0.11 for mussel samples and between 0.26 and 0.72 for sediment samples. These values show that isotope dilution-GC-ICPMS methodology is valid for the determination of MBT, DBT and TBT from both types of matrices. 相似文献
14.
The highly qualified primary method of species-specific isotope dilution analysis has been employed in this work to evaluate for the first time the levels of butyltin compounds in the estuary of the river Eo (Northwest Spain) where there is, since many years, a high oyster farming activity. A spike solution containing mono-, di- and tributyltin enriched in 119Sn allowed the simultaneous determination of the three compounds in different marine environmental and biological samples collected in this area (seawater samples, sediments and biological tissues of four different marine species). The results obtained in this work showed toxic TBT levels for many marine species in 45% of the seawater samples analyzed whereas significant organotin concentrations were found to be obtained only in one of the sediments analyzed. On the other hand, TBT levels ranging from 20 to almost 200 ng g− 1 (dry weight) were obtained in the different biological tissues analyzed demonstrating the bioaccumulation of organotin compounds in certain marine species. 相似文献
15.
16.
The performance of solid-phase microextraction (SPME) applied to the determination of butyltin compounds in sediment samples is systematically evaluated. Matrix effects and influence of blank signals on the detection limits of the method are studied in detail. The interval of linear response is also evaluated in order to assess the applicability of the method to sediments polluted with butyltin compounds over a large range of concentrations. Advantages and drawbacks of including an SPME step, instead of the classic liquid–liquid extraction of the derivatized analytes, in the determination of butyltin compounds in sediment samples are considered in terms of achieved detection limits and experimental effort. Analytes were extracted from the samples by sonication using glacial acetic acid. An aliquot of the centrifuged extract was placed on a vial where compounds were ethylated and concentrated on a PDMS fiber using the headspace mode. Determinations were carried out using GC-MIP AED. 相似文献
17.
The present publication describes a microwave-assisted digestion procedure for the subsequent trace and ultra-trace analysis of palladium in road dust of varying origin. Digestion reagents are nitric acid, hydrogen peroxide and hydrofluoric acid. Boric acid is used as masking agent for fluoride ions to avoid removal of excess hydrofluoric acid by vaporization. After the three-step digestion procedure, a colorless and residue-free solution is obtained in which the determination of palladium can be directly performed using a recently developed highly selective on-line pre-concentration system, coupled with graphite furnace atomic absorption spectrometry (GF-AAS). Dust samples of varying origin (tunnel dust, road dust, filter dust from Frankfurt, Munich and Japan) and sampling dates (1987-2001) were investigated and characterized in detail with respect to matrix composition and palladium content. Validation of the analytical results was performed by recovery experiments. 相似文献
18.
We have devised a new method for bis(tributyltin)oxide (TBTO) determination in marine sediments and mussels. This technique involves an n-hexane/methylene chloride mixture extraction and extract purification with a sodium hydroxide wash in order to eliminate interfering compounds. TBTO is then extracted again by nitric acid and converted into an inorganic tin species; the analysis has been effected using Zeeman graphite furnace-atomic absorption spectrophotometry. The method detection limit for the matrices examined is 0.004 μg TBTO g?1 (wet weight) and is sufficient for the analysis in real samples. The percentage recovery of TBTO from sediments and mussels samples is higher than 85% and 95% respectively. This method has been applied to TBTO level determination in sediments and mussels (Mytilus galloprovincialis) sampled in the harbour area in Taranto, where mussel culture activities are much developed; the TBTO levels obtained in sediments and mussels were in the range 15-47 ng g?1 (wet weight) and 11-30 ng g?1 (wet weight) respectively. Such values are comparable with those found in other harbour areas in the Mediterranean Sea. 相似文献
19.
Nanogram quantities of heavy metals in 200 ml of water were quantitatively preconcentrated by coprecipitation with magnesium oxinate at pH 9–9.5. The precipitate was collected on a 1-m Nuclepore membrane filter and then dissolved in 5 ml of 1 mol/l nitric acid. After diluting to 10 ml with water, a 10- or 20-l aliquot of the solution was directly analyzed by electrothermal atomic absorption spectrometry using deuterium background correction. The background absorption due to the collector magnesium oxinate was negligibly small. The optimized coprecipitation technique has been applied to the determination of cobalt, nickel, copper, cadmium and lead at the ppt level in river and seawater. The relative standard deviations were within 10% and the detection limits were 0.025 (for Co), 0.019 (for Ni), 0.006 (for Cu), 0.001 (for Cd) and 0.017 g/l (for Pb). Blanks through the whole procedure were not detectable. 相似文献
20.
Ján Medved’ Milan Kališ Ingrid Hagarová Peter Matúš Marek Bujdoš Jana Kubová 《Chemical Papers》2008,62(2):168-175
Determination of thallium in polluted environmental samples and their extracts obtained by a modified BCR three-step sequential
extraction procedure was used to study thallium distribution and mobility in the monitored polluted area affected by acidification
(Šobov, Central Slovakia). The results of fractionation applied to 5 soil certified reference materials and 14 environmental
samples show that the vast majority of thallium occurred in the residual fraction. This means that highly toxic thallium is
strongly entrapped in the parent rock materials remains immobile and its environmental toxicity is therefore reduced. The
limit of detection for thallium in the studied fractions was lower than 0.050 mg kg−1, the precision (RSD) of the ultratrace determination of thallium in the studied fractions was better than 17 % and the accuracy
of the used method was verified by analyzing certified reference materials.
Presented at the XVIIIth Slovak Spectroscopic Conference, Spišská Nová Ves, 15–18 October 2006. 相似文献