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31.
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
32.
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
33.
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
34.
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
35.
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
36.
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
37.
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
38.
Juliana Vaz Bevilaqua Lidia M. Lima Aline Gomes Cunha Eliezer J. Barreiro Tito L. M. Alves Lucia Moreira Campos Paiva Denise M.Guimarães Freire 《Applied biochemistry and biotechnology》2005,121(1-3):117-128
The last step of the production of four phthalimide-derived acids, designed to act as antiasthma drugs, was performed by enzymatic hydrolysis of the respective methyl or ethyl esters. The esters 4-ethyl-[2-(1,3-dioxo-1,3-dihydro-2-isoindoylyl)]-phenoxyacetic methyl ester (PHT-MET), 4-ethyl-[2-(1,3-dioxo-1,3-dihydro-2-isoindoylyl)]-phenoxyacetic ethyl ester, 4-(1,3-dioxo-1,3-dihydro-2-isoindoylyl)-phenoxyacetic ethyl ester, and 2-(1,3-dioxo-1, 3-dihydro-2-isoindoylyl)-phenoxyacetic ethyl ester were hydrolyzed by immobilized lipase. The enzymatic reaction could be used only to produce the desired 4-substituted compounds. The best result that was found to hydrolysis of PHT-MET, and, therefore, that ester was selected for optimization experiments in a three-phase system. Reactions were performed with solid biocatalyst (Lipozyme® RM IM), organic solvent phase (ethyl acetate), and aqueous phase (saturated Na2CO3 solution). To optimize the reaction conditions, an experimental design optimization procedure was used. The variables studied were the amount of enzyme, the temperature, and the volume of the aqueous solution. Time course experiments were then performed for different initial enzyme concentrations (0.5, 0.9, and 1.4 UH/mL of solvent). The optimized reaction conditions found were 20 mg of Lipozyme (0.9 UH/mLsolvent) and 5.0 mL of Na2CO3(sat) at 40°C for 6 h. 相似文献
39.
do Nascimento Filho I Schossler P Santos Freitas L Melecchi MI Rodrigues Vale MG Bastos Caramão E 《Journal of chromatography. A》2004,1027(1-2):167-170
In this work a simple method was described for selective extraction of benzoic acid from landfill leachate samples. The samples were submitted to solid-phase extraction (SPE) with XAD-4 resin as the stationary phase and ion-exchange chromatography (IEC) using the ion-exchange resin Amberlyst A-27. The instrumental analysis was performed by gas chromatography with mass spectrometric detection (GC-MSD). Benzoic acid was isolated, identified and quantified. The extraction process is rapid, simple and of low cost. It was also environmental friendly, that is, it was used a minimum amounts of hazardous organic solvents and produced also minimum quantities of residues. 相似文献
40.
Mojca Dobnikar Marijan Kočevar Andrej Petrič Miha Tišler Bojan Verček 《Monatshefte für Chemie / Chemical Monthly》1989,120(3):269-272
Summary Syntheses of 1-methylimidazo[1,2-c]quinazolinium iodide (3) and 1-methylimidazo[2,1-f]pyrido[3,2-d]pyrimidinium iodide (4) are described. These tricyclic compounds react with nucleophiles derived from active methylene compounds to give the corresponding open-chain enamines.
Reaktionen von quaternisierten Imidazo-Chinazolinen und -Pyridopyrimidinen mit Verbindungen mit reaktiven Methylengruppen
Zusammenfassung Synthesen von 1-Methylimidazo[1,2-c]chinazoliniumjodid (3) und 1-Methylimidazo[2,1-f]pyrido[3,2-d]pyrimidiniumjodid (4) werden beschrieben. Diese tricyclischen Verbindungen reagieren mit einigen Carbanionen aus Verbindungen mit reaktiven Methylengruppen, wobei die offenkettigen Enamine entstehen.相似文献