Search results for "Microwave oven"
showing 10 items of 25 documents
Hydride generation atomic fluorescence spectrometric determination of ultratraces of selenium and tellurium in cow milk
2003
Abstract A sensitive procedure has been developed for selenium and tellurium determination in milk by hydride generation atomic fluorescence spectrometry (HG-AFS) after microwave-assisted sample digestion. The method provides sensitivity values of 1591 and 997 fluorescence units ng−1 ml−1 with detection limits of 0.005 and 0.015 ng ml−1 for Se and Te, respectively. The application of the developed methodology to the analysis of cow milk samples of the Spanish market evidenced the presence of concentration ranges from 11.1 to 26.0 ng ml−1 for Se, and from 1.04 to 9.7 ng ml−1 for Te having found a good comparability with data obtained after dry-ashing of samples.
Determination of mercury in dry-fish samples by microwave digestion and flow injection analysis system cold vapor atomic absorption spectrometry
1997
Abstract Flow injection analysis system cold vapor atomic absorption spectrometry (FIAS-CV-AAS) preceded by a wet digestion in a microwave oven, as a method for measuring mercury in fish was studied. The digestion process and conditions of the FIAS (carrier concentration: HCl 3% v v ; reducing agent: SnCl2 2% w v : filling and injection times: 8 and 25 min, respectively; and sample volumes) were optimized. The analytical parameters of the proposed method (detection limit = 7.7 ng/g; precision intraassay = 6.7%; interassay = 14.0%) demonstrates its adequacy and are similar to the ones (detection limit = 19.4 ng/g; precision intraassay = 11.2%; interassay = 15.9%) obtained using a conventiona…
Multicommutation hydride generation atomic fluorescence determination of inorganic tellurium species in milk
2005
Abstract A multicommutated flow system has been developed for hydride generation, atomic fluorescence (HG-AFS) determination of tellurate (Te VI ) and tellurite (Te IV ) in milk samples. After a batch leaching of Te by sonication at room temperature for 10 min with aqua regia, sample slurries in acidic medium were merged with sodium borohydride and HCl to obtain data on Te IV . Another portion of the acidic slurry was mixed with KBr and passed through a reaction coil introduced inside a microwave oven to reduce quantitatively Te VI to Te IV which was analyzed by HG-AFS. The detection limit was 0.57 ng g −1 in the original samples. The linear range obtained was till 4 ng ml −1 and the averag…
Microwave-assisted vapour-generation Fourier transform infrared spectrometric determination of carbonate in waters
1998
Abstract A microwave-assisted vapour-generation Fourier transform infrared spectrometric procedure is proposed for the determination of total carbonate in waters. The method is based on the simultaneous injection of 100 μl of sample and 300 μl of 0.1 M nitric acid in a two-channel manifold with a merging zone; a coil located inside a microwave oven encourages the removal of CO 2 . The carbon dioxide is separated from the distilled water employed as carrier by means of gas–liquid separator and is introduced by a nitrogen carrier flow inside a long-path infrared absorption gas cell, from which the corresponding flow analysis recording is registered as a function of time in the wavenumber rang…
Determination of mercury in rice by cold vapor atomic fluorescence spectrometry after microwave-assisted digestion.
2010
Abstract A cold vapor atomic fluorescence spectrometry method (CV-AFS) has been developed for the determination of Hg in rice samples at a few ng g−1 concentration level. The method is based on the previous digestion of samples in a microwave oven with HNO3 and H2O2 followed by dilution with water containing KBr/KBrO3 and hydroxylamine and reduction with SnCl2 in HCl using external calibration. The matrix interferences and the effect of nitrogen oxide vapors have been evaluated and the method validated using a certified reference material. The limit of detection of the method was 0.9 ng g−1 with a recovery percentage of 95 ± 4% at an added concentration of 5 ng g−1. The concentration level …
GFAAS determination of selenium in infant formulas using a microwave digestion method.
1994
A method for determining the selenium content of infant formulas is proposed. It includes wet digestion with nitric acid and hydrogen peroxide in medium pressure teflon bombs in a microwave oven and determination by graphite furnace atomic absorption spectrometry (GFAAS). The absence of interferences is checked. Values obtained for the limit of detection (19.4 ng/g), precision (RSD = 2.2%) and accuracy by analysis of a reference material show that the method is reliable.
Atomic fluorescence determination of inorganic arsenic in soils after microwave-assisted distillation
2000
Abstract An inexpensive microwave-assisted distillation procedure has been developed for quantitative determination of inorganic arsenic in soils by atomic fluorescence spectrometry (AFS). After reduction of As(V) to its trivalent state with potassium iodide, inorganic arsenic was distilled as AsCl 3 that was finally determined by atomic fluorescence after hydride generation with NaBH 4 in HCl medium. The different parameters that control the distillation: concentration and volume of HCl, time of distillation, sample weight, and oven load, were studied. The methodology developed has a detection limit of 0.015 μg l −1 , which corresponds to a concentration of 0.006 μg of As per gram of soil,…
Determination of essential metals in complete diet feed by flow injection and flame atomic absorption spectrometry
2002
A prior study of different sample pre-treatments for the determination of metallic elements in complete diet feeds was performed in order to choose the most suitable for these samples. The studied pre-treatment were: acid extraction (lixiviation), wet digestion (on microwave oven) and dry ashing mineralization (calcination). Lixiviation (acid extraction) with hydrochloric acid was selected due to its accuracy, fast and simple pre-treatment procedure. Due of the different levels of concentration of the metallic elements in the samples, the same manifold was used but with small variations. Copper (with on-line pre-concentration by chelating Chelex-100 resin), calcium (with on-line dilution) a…
Rapid on-line sample dissolution assisted by focused microwave radiation for silicate analysis employing flame atomic absorption spectrometry: iron d…
2004
An on-line automated flow injection system with microwave-assisted sample digestion was used to perform silicate rock dissolution in acid medium for iron determination. For this purpose, a continuous flow system was built up by using an automatic flow injection analysis (FIA) system coupled to a flame atomic absorption spectrometer (FAAS), including a focused microwave oven unit. Inside the microwave cavity was inserted a polytetrafluoroethylene (PTFE) reactor coil (300cm length and 0.8mm i.d.) where the dissolution takes place. Chemical and flow variables as well as iron determination parameters were studied. In the flow system, a slurry of the rock sample (50mg in 200ml of acid mixture HF…
Microwave muffle furnace assisted decomposition of vegetable samples for flame atomic spectrometric determination of Ca, Mg, K, Fe, Mn and Zn
1992
Calcium, magnesium, potassium, iron, manganese and zinc can be accurately determined in vegetable samples by flame atomic absorption and flame emission spectrophotometry after a previous dry ashing of the sample in a microwave muffle furnace. This treatment is carried out in 45 min using a new accessory developed by us to obtain high temperatures on a domestic microwave oven. Sample ashes, obtained in the muffle, are diluted with nitric acid and the obtained slurry is introduced directly into an air-C2H2 flame for the analysis of Fe, Mn, and Zn, or injected into a double-channel FIA manifold to determine Ca, Mg and K. The obtained results agree with those certified and also with those obtai…