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1.
J Autom Methods Manag Chem ; 22(3): 83-8, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-18924860

RESUMO

A low inner volume (ca. 64 ml) probe was built up in an injector-commutator in order to behave as a photometric leaping detector in flow analysis. It comprises a bicolour light-emitting diode (BLED), as a source of pulsed radiation in the red and green visible region, and two phototransistors as transducers. Sample injection, detector relocation, analytical signal recording, data treatment and definition of the spectral working range were computer-controlled. The feasibility of the system was initially demonstrated in the flow-injection speciation of iron, and the overall standard deviation of results was estimated as +/- 1.6 and +/- 1.4% for 1.6-4.0 mg l(-1) Fe(II) or total iron after eightfold processing of synthetic samples. The system was further applied to drug analysis: the mean deviations of results for typical samples were estimated as +/- 5.2 and +/- 3.3%, and the relative standard deviation as +/- 1.6 and +/- 1.3% for Fe(II) and total iron, respectively. Results were compared with those obtained by a conventional spectrophotometric procedure and no statistic differences at the 95% confidence level were found. In relation to an earlier system with multi-site detection, the proposed system is more stable, presenting low drift with a relative standard deviation of 0.026% and 0.039% for measurements (n=120 during 4 h of observation) with green and red emission. It is also faster with a sampling rate of 133 h(-1) and carryover problems are not found. The possibility of compensating the Schlieren noise by dual-wavelength spectrophotometry is discussed.

2.
Fresenius J Anal Chem ; 368(5): 496-500, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11227532

RESUMO

A flow-batch system allowing in-line individual sample matrix matching is proposed for analysis of sample lots with high variability in acidity. The feasibility of the approach is demonstrated in the spectrophotometric determination of total nitrogen in Kjeldahl digests, using a column with a slightly soluble reagent (AgCl). The solutions are sequentially injected by means of an 8-port selecting valve and processed in a mixing chamber that is also used as a monitoring unit. The system yields reproducible results (r.s.d. usually < 2.5%) and the sampling rate is 14 samples/h. The analytical curve is linear within 1.00 and 6.00% N (dry basis), and the regression coefficient is > 0.999 (n = 6). Results are in agreement with certified values of standard reference materials and with results obtained by conductometry.


Assuntos
Análise de Alimentos/métodos , Nitrogênio/análise , Extratos Vegetais/análise , Ácidos/análise , Citrus/química , Café/química , Análise de Alimentos/normas , Oryza/química , Sensibilidade e Especificidade , Glycine max/química , Análise Espectral
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