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31.
32.
M. C. Freitas M. M. Farinha A. M. G. Pacheco M. G. Ventura S. M. Almeida M. A. Reis 《Journal of Radioanalytical and Nuclear Chemistry》2005,263(3):710-720
Summary Selenium is determined by instrumental neutron activation analysis (INAA), based on measurement of the long-lived 75Se nuclide. In the urban and industrialized areas of Portugal selenium contents have been found of the order of of 0.5-1 ng/m3 in PM10 and PM2.5, according to the data collected since 1994. From November 12, 2001 and for not more than 3 months, the Se contents in PM10 and PM2.5 increased by a factor of 1000 in the northern area of Lisbon. More than other nutrients, selenium illustrates the dichotomy between essentiality and toxicity. There is no legislation on Se for ambient air and on indoor ambient point threshold limit values (US and Germany legislation), were 100 times higher than the abnormal values found that winter. The increase was also visible for mercury although not to such an extent. Attempts were made to understand the trend, going into a study of the emission sources located in the area using both INAA and PIXE. It was concluded that the observation occurred due to abnormal meteorological wind direction, which pushed the pollutants towards the populated area, when usually they flow into the Tagus estuary. 相似文献
33.
We describe a simple method for the determination of phenobarbital, diphenylhydantoin, carbamazepine, and primidone in serum, by use of gas-liquid chromatography with temperature programming. The methylated derivatives of these anticonvulsants were well resolved, as was 5-(p-methylphenyl)-5-phenylhydantoin, the internal standard. In this procedure we used the jet tube for separation of the drug from the serum. The proposed procedure requires only 100 μl of serum and can be done in less than 30 min. The lower limit of detection for each of the drugs is 0.5 mg/liter. Analytical recoveries of drug from serum were excellent and peak height and concentration were linearly related up to twice the toxic concentration for serum. 相似文献
34.
V. R. S. Rao G. Erdtmann H. Petri 《Journal of Radioanalytical and Nuclear Chemistry》1989,135(4):257-264
The extent of exchange of bromine-82 with bromamine-T in strong acid medium is low due to the formation of
at lower acid concentrations and bromine at higher acidities.
formation occurs over a narrow acid concentration range and is less stable than
. 相似文献
35.
M. C. Freitas A. M. G. Pacheco E. Ferreira 《Journal of Radioanalytical and Nuclear Chemistry》2006,270(1):123-130
The present study aims the identification and quantification of trace elements in samples of honey from the Azores and the
Portuguese mainland. Elemental concentrations were determined for Al, Br, Cl, Cs, Cu, Eu, Fe, K, Mg, Mn, Na, Rb, Sb, and Zn.
Some of these elements are essential dietary nutrients for humans. The essential elements, K and to a lesser extent Na and
Cl were the most abundant in the honey samples. However, overall, the elemental content was very low, inferior to the recommended
allowances for daily dietary intake (DDI), with the exception of Na whose concentration exceeded that of the recommended DDI.
The results of the present investigation and data reported for other countries compare well. The honeys correlate much better
when they are from Azores or from Portugal mainland, however, some good correlations were found between honeys from the islands
and the mainland. The color of the honey, which depends of the flower-source, could have a role in the differences and similarities
between the different honeys as suggested by the cluster analysis of the data. The correlation between honey, soil, tree bark
and lichens, all collected in Azores, was poor. 相似文献
36.
We report here our findings on a new and highly efficient strategy for the synthesis of β-amino acids involving the addition of bis(O-silyl) ketene acetals on Mannich type iminium electrophiles. 相似文献
37.
L. C. Machado A. A. L. Marins E. J. B. Muri J. A. S. Lacerda V. O. Balthar P. F. Fulvio J. C. C. Freitas 《Journal of Thermal Analysis and Calorimetry》2004,75(2):615-621
This paper presents the reactions of synthesis between the ligand sodium diphenylamine-4-sulfonate and the lanthanum(III)
chloride hydrated. The compounds (LaCl3)2·(C12H10NSO3Na)3·2(CH3CH2OH) (A) and (LaCl3)·(C12H10NSO3Na)·(CH3CH2OH)·12H2O (B) were obtained using the solvents ethanol and methanol (synthesis A) and ethanol and water (synthesis B). The produced
compounds and the ligand were characterized by thermogravimetric and differential thermogravimetric analysis, IR spectroscopy
and elemental analysis of sodium, carbon, hydrogen, nitrogen, sulfur, chlorine and lanthanum, whereas the residues from thermal
decomposition were investigated by X-ray diffractometry.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
38.
Rafael Fogel Rafaela Rodrigues Garcia Rebeca da Silva Oliveira Denise Neves Menchero Palacio Luciana da Silva Madeira Nei Pereira Jr. 《Applied biochemistry and biotechnology》2005,122(1-3):741-752
The dilute-acid hydrolysis of sugarcane bagasse was optimized using a statistical experimental design resulting in hydrolysates
containing 57.25 g/L of xylose, which were fermented with a high inoculum concentration (10 g/L of the yeast Candida guilliermondii IM/UFRJ 50088). The addition of urea reduced the time of conversion (t
C) to 75 h (without nitrogen source addition t
C>127 h), and, consequently, improving the rates of xylitol bioproduction. Fermentator experiments, using the optimized conditions,
resulted in enhanced conversion rates, reducing t
C to 30 h. The stability of the yeast in the hydrolysate was also verified in a 480-h cultivation. 相似文献
39.
Denise Bohrer Uwe Heitmann Mao-dong Huang Helmut Becker-Ross Stefan Florek Bernhard Welz Denise Bertagnolli 《Spectrochimica Acta Part B: Atomic Spectroscopy》2007
High-resolution continuum source atomic absorption spectrometry (HR-CS AAS) has been used to investigate spectral and non-spectral interferences found with a conventional line source atomic absorption spectrometer in the determination of aluminum in pharmaceutical products containing elevated iron and sugar concentrations. A transversely heated graphite furnace was used as the atomizer in both spectrometers. The two most sensitive aluminum lines at 309.3 nm and 396.2 nm were investigated and it was found that an iron absorption line at 309.278 nm, in the vicinity of the aluminum line at 309.271 nm, could be responsible for some spectral interference. The simultaneous presence of iron and the organic components of the matrix were responsible for radiation scattering, causing high continuous and also structured background absorption at both wavelengths. The aluminum and iron absorption could not be separated in time, i.e., the iron interference could not be eliminated by optimizing the graphite furnace temperature program. However, an interference-free determination of aluminum was possible carrying out the measurements with HR-CS AAS at 396.152 nm after applying least squares background correction for the elimination of the structured background. Analytical working range and other figures of merit were determined and are presented for both wavelengths using peak volume registration (center pixel ± 1) and the center pixel only. Limits of detection and characteristic masses ranged from 1.1 to 2.5 pg and 13 to 43 pg, respectively. The method was used for the determination of the aluminum contamination in pharmaceutical formulations for iron deficiency treatment, which present iron concentrations from 10 to 50 g l− 1. Spike recoveries from 89% to 105% show that the proposed method can be satisfactorily used for the quality control of these formulations. 相似文献
40.
A universal temperature controlled membrane interface (TCMI) has been constructed for hollow-fibre membranes. The membrane temperature is controllable in the range -70 to 250 degrees C using an electric heater and a flow of cooled nitrogen or helium gas. Volatile and semi-volatile organic compounds may be detected either by continuous diffusion across the membrane or by in-membrane pre-concentration followed by thermal desorption into the detector. The TCMI interface is demonstrated in combination with mass spectrometry and GC-MS, for the determination of VOCs and SVOCs in aqueous and air samples and for the on-line monitoring of a bioreactor. 相似文献