ABSTRACT
Laser ablation coupled to inductively coupled plasma optical emission spectrometry (LA-ICP-OES) and laser-induced breakdown spectroscopy (LIBS) were investigated for the determination of Ca, Mg, Zn and Na in milk samples. The accuracy of both methods was evaluated by comparison of the concentration found using LA-ICP-OES and LIBS with classical wet digestion associated with ICP-OES determination. The results were not fully acceptable, with biases from less than 1% to more than 60%. Matrix effects were also investigated. The sample matrix can influence the temperature, electron number density (n (e)) and other excitation characteristics in the ICP. These ICP characteristics were studied and evaluated during ablation of eight milk samples. Differences in n (e) (from 8.9 to 13.8 × 10(14) cm(-3)) and rotational temperature (ranging from 3,400 to 4,400 K) occurred with no correlation with trueness. LIBS results obtained after classical external calibration procedure gave degraded accuracy, indicating a strong matrix effect. The LIBS measurements clearly showed that the major problem in LA-ICP was related to the ablation process and that LIBS spectroscopy is an excellent diagnostic tool for LA-ICP techniques.
Subject(s)
Milk/chemistry , Powders/chemistry , Spectrophotometry, Atomic/standards , Spectrum Analysis/standards , Animals , Calcium/analysis , Calibration , Female , Lasers , Magnesium/analysis , Sensitivity and Specificity , Sodium/analysis , Spectrophotometry, Atomic/methods , Spectrum Analysis/methods , Temperature , Zinc/analysisABSTRACT
The retention of organic selenium compounds on a porous graphitic carbon stationary phase was investigated. Different acids were studied as mobile phases to elute selenocystamine, selenoethionine, selenomethionine and selenocystine. Detection was achieved using inductively coupled plasma-atomic emission spectrometry to provide selenium-specific and sensitive detection. The separation of the four species was carried out using methanoic acid. An important on-column preconcentration was obtained when solutes were injected in nitric acid or trifluoroacetic acid (TFA) media. The large injection volume employed (2,500 micro L) allowed us to reach low relative detection limits (2-6 micro g/L). The method, employing TFA as injection solvent and methanoic acid as the eluent was found to be robust with respect to different matrices spiked with selenocompounds.
Subject(s)
Chromatography, High Pressure Liquid/methods , Graphite/chemistry , Selenium Compounds/isolation & purification , Buffers , Calibration , Hydrogen-Ion Concentration , Porosity , Selenium Compounds/analysis , Sensitivity and Specificity , Yeasts/chemistryABSTRACT
A new liquid chromatographic separation method was developed for the speciation of the four main arsenic compounds present in water. Arsenite (As(III)), dimethylarsinic acid (DMA), monomethylarsonic acid (MMA) and arsenate (As(V)) were separated on a recently introduced stationary phase: porous graphitic carbon (PGC). The separation was first obtained under formic acid gradient conditions, but an adsorption phenomenon of As(V) on PGC was observed. To overcome this problem, As(V) was backflushed, and an efficient separation of the four solutes was achieved within 10 min. Extremely low detection limits (ranging from 10 to 70 ng x L(-1)) were obtained by coupling LC with an ICPMS. The method was successfully applied to different spiked mineral waters and a naturally arsenic-containing freshwater.
ABSTRACT
High performance liquid chromatography coupled to ICP-AES detection provides a rapid, reliable and sensitive method for arsenic speciation. The separation of As(III), As(V), DMA and MMA was achieved with ion exchange chromatography coupled to an axially-viewed sequential ICP-AES. After optimization of the chromatographic parameters (pH and concentration of the mobile phase), a careful study of the interface was conducted. Five nebulizers associated to three spray chambers were tested. Response of the ICP to each arsenic species was strongly affected by the selection of the nebulizer and spray chamber, however similar responses were obtained for each arsenic species. Best signal-to-noise ratios were obtained by using a microconcentric nebulizer and a cyclone spray chamber and did not affect the chromatographic resolution. Detection limits better than 10 microg L(-1) were obtained for As(III), DMA, MMA and 20 microg L(-1) for As(V), which is a significant improvement over previously published results.
