Fluorimetric determination of beryllium with 3-hydroxy-2-naphthoic acid by flow injection analysis after preconcentration on a silica gel microcolumn

1989 ◽  
Vol 54 (7) ◽  
pp. 1777-1784 ◽  
Author(s):  
Vlastimil Kubáň ◽  
Josef Havel ◽  
Bronislava Patočková

A method was worked out for the selective determination of trace concentrations of beryllium by flow injection analysis (FIA) with fluorimetric detection using 3-hydroxy-2-naphthoic acid (λex = 375 nm, λem = 455 nm) at cL = 50 μmol l-1 in 0.1M ammonium acetate, pH 7·1. In injected sample volumes of 80 μl, Be can be determined in concentrations of 10 to 156 μg l-1 with relative standard deviations not exceeding 5%, after its selective sorption on a microcolumn (2 x 40 or 3 x 30 mm) of silica gel from a medium of 0.05M-EDTA and 0.1M tartaric acid followed by elution with 0.1M-HCl. After preconcentration from 5 to 15 ml volumes, Be can be determined under the same conditions in samples at concentrations of ρBe = 0.5 to 4.6 or 0.1 to 0.8 μg l-1, respectively, with sr from 6 to 12%, the enrichment factor being as high as 200. The method was applied to beryllium bronzes and to dust from the atmosphere of the beryllium bronze foundry. The relative deviations of the beryllium content did not exceed 8% for the bronzes as compared to certified values, and 5% for the dust as compared to results obtained by ETA AAS.

1987 ◽  
Vol 35 (3) ◽  
pp. 315-320 ◽  
Author(s):  
Baldomero Bermúdez ◽  
Fernando Lázaro ◽  
M.Dolores Luque de Castro ◽  
Miguel Valcárcel

1988 ◽  
Vol 332 (7) ◽  
pp. 809-812 ◽  
Author(s):  
Fernando Lazaro ◽  
M. Dolores Luque de Castro ◽  
Miguel Valcarcel

1990 ◽  
Vol 23 (12) ◽  
pp. 2315-2325 ◽  
Author(s):  
J. Martinez Calatayud ◽  
A. Sanchez Sampedro ◽  
P. Villar Civera ◽  
C. Gomez Benito

1980 ◽  
Vol 26 (2) ◽  
pp. 331-334 ◽  
Author(s):  
B W Renoe ◽  
K K Stewart ◽  
G R Beecher ◽  
M R Wills ◽  
J Savory

Abstract We describe an adaptation of automated multiple flow-injection analysis instrumentation to an analysis for albumin in serum. The bromcresol green reaction was used to test the utility of the system. The approach yielded albumin results with excellent sensitivity, no measurable carryover, a relative standard deviation of less than 1%, good correlations with published procedures, and no measurable interferences. The simplicity and flexibility of the instrumentation and its performance integrity, as indicated by the analytical results, make this a viable clinical chemical tool.


1996 ◽  
Vol 79 (3) ◽  
pp. 764-768 ◽  
Author(s):  
Oroncio Jiménez De Blas ◽  
N Rodriguez Mateos ◽  
A Garcia Sanchez

Abstract A procedure has been developed for determination of total arsenic and selenium in soils and plants by atomic absorption spectrometry with hydride generation associated with flow injection analysis (FIA-AAS-HG). Samples were wet-digested by using 2 systems: heating in a metal digestion block with controlled temperature and time and heating in a microwave oven. Total arsenic and selenium were reduced with NaBH4 and concentrated HCI, respectively. In both digestion systems used for the 2 matrix types, detection limits below 1 μg/L were found for both elements for an injection volume of 160 μL, with relative standard deviations of 3–6%. Recoveries by the method ranged from 93 to 105%; with the reference materials FD8 and MRG-1, the values obtained in all cases were consistent with the certified data. The FIA-AAS-HG procedure is highly suitable for determination of total arsenic and selenium in soils and plants, and because of the coupled system used, it is an improvement over other procedures in terms of sample treatment, sample consumption, and automation.


2002 ◽  
Vol 372 (2) ◽  
pp. 387-390 ◽  
Author(s):  
Tomás Pérez-Ruiz ◽  
Carmen Martínez-Lozano ◽  
Virginia Tomás ◽  
Jesús Martín

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