RESUMO
A fully automated multipumping flow system (MPFS) using water-soluble CdTe quantum dots (QD) as sensitizers is proposed for the chemiluminometric determination of the anti-diabetic drugs gliclazide and glipizide in pharmaceutical formulations. The nanocrystals acted as enhancers of the weak CL emission produced upon oxidation of sulphite by Ce(IV) in acidic medium, thus improving sensitivity and expanding the dynamical analytical concentration range. By interacting with the QD, the two analytes prevented their sensitizing effect yielding a chemiluminescence quenching of the Ce(IV)-SO(3)(2-)CdTe QD system. The pulsed flow inherent to MPFS assured a fast and efficient mixing of all solutions inside the flow cell, circumventing the need for a reaction coil and facilitating the monitoring of the short-lived generated chemiluminescent species. QD crystal size, concentration and spectral region for measurement were investigated.
RESUMO
A novel flow-based strategy for implementing simultaneous determinations of different chemical species reacting with the same reagent(s) at different rates is proposed and applied to the spectrophotometric catalytic determination of iron and vanadium in Fe-V alloys. The method relies on the influence of Fe(II) and V(IV) on the rate of the iodide oxidation by Cr(VI) under acidic conditions; the Jones reducing agent is then needed. Three different plugs of the sample are sequentially inserted into an acidic KI reagent carrier stream, and a confluent Cr(VI) solution is added downstream. Overlap between the inserted plugs leads to a complex sample zone with several regions of maximal and minimal absorbance values. Measurements performed on these regions reveal the different degrees of reaction development and tend to be more precise. Data are treated by multivariate calibration involving the PLS algorithm. The proposed system is very simple and rugged. Two latent variables carried out ca 95% of the analytical information and the results are in agreement with ICP-OES.
RESUMO
Multi-pumping flow systems exploit pulsed flows delivered by solenoid pumps. Their improved performance rely on the enhanced radial mass transport inherent to the pulsed flow, which is a consequence of the establishment of vortices thus a tendency towards turbulent mixing. This paper presents several evidences of turbulent mixing in relation to pulsed flows, such as recorded peak shape, establishment of fluidized beds, exploitation of flow reversal, implementation of relatively slow chemical reactions and/or heating of the reaction medium. In addition, Reynolds number associated with the GO period of a pulsed flow is estimated and photographic images of dispersing samples flowing under laminar regime and pulsed flow conditions are presented.
RESUMO
The concept of multi-commutation in flow analysis is revisited, and emphasis is given to recent methodological and applicative achievements. Multi-commutation is compatible with different flow patterns (unsegmented, segmented, pulsed, tandem) and amenable to concentration-oriented feedback mechanisms. Its exploitation has led to significant attainments mainly in relation to versatility of the flow system. Characteristics and potentialities of the multi-commuted flow systems are discussed, and guidelines for assisting methodological implementation are given. The number of applications has experienced remarkable increase during last years; therefore, the applicative part of this review is focused on the recent noteworthy applications, mainly in relation to environmental, agronomical, pharmaceutical, biological, food and industrial samples.
Assuntos
Análise de Injeção de Fluxo , Animais , Simulação por Computador , Desenho de Equipamento , Análise de Injeção de Fluxo/instrumentação , Análise de Injeção de Fluxo/métodos , Humanos , Hidroquinonas/análise , Metais/análise , Compostos Orgânicos/análise , Sensibilidade e Especificidade , Sulfetos/análise , Ácido Úrico/urinaRESUMO
Differential kinetic analysis can be implemented in a multi-pumping flow system, and this was demonstrated in relation to an improved spectrophotometric catalytic determination of iron and vanadium in Fe-V alloys. The method exploited the influence of Fe(II) and V(IV) on the rate of iodide oxidation by Cr(VI) under acidic conditions; therefore the Jones reductor was needed. The sample was inserted into an acidic KI stream that acted also as carrier stream, and a Cr(VI) solution was added by confluence. Successive measurements were performed during sample passage through the detector, each one related to a different yet reproducible condition for reaction development. Data treatment involved multivariate calibration by the PLS algorithm. The proposed system is very simple and rugged, allowing about 50 samples to be run per hour, meaning 48 mg KI per determination. The first two latent variables carry ca. 94% of the analytical information, pointing out that the intrinsic dimensionality of the data set is two. Results are in agreement with inductively coupled argon plasma-optical emission spectrometry.
RESUMO
A flow-injection procedure for simultaneous spectrophotometric determination of tungsten and molybdenum in steel alloys is proposed. The method exploits the catalytic effects of Mo(VI) and W(VI) on the rate of iodide oxidation by hydrogen peroxide under acidic conditions. A novel strategy for ion-exchange separation of the potential interfering species is proposed, and an AG50W-X8 cationic resin mini-column is used. The sample is injected twice, originating two sequential plugs, citrate being added to one of them in order to suppress the W(VI) catalytic activity thus providing the kinetic discrimination. The system handles 70 samples per hour and requires 1.6mg KI per determination. A linear response is verified up to 10mgl(-1) Mo (or W) in the injectate, and signal additivity is 98-103%. Results are precise (R.S.D.<0.04) and in agreement with ICP-OES. Running a standard reference material (IPT-50) assessed also accuracy.