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121.
122.
123.
Santos E 《Physical review letters》1991,66(11):1388-1390
124.
Emilio Santos 《International Journal of Theoretical Physics》1992,31(10):1909-1913
The problem of hidden variables in quantum mechanics is formalized as follows. A general or contextual (noncontextual) hidden-variables theory is defined as a mappingf: Q×M C (f: QC) whereQ is the set of projection operators in the appropriate (quantum) Hilbert space,M is the set of maximal Boolean subalgebras ofQ andC is a (classical) Boolean algebra. It is shown that contextual (noncontextual) hidden-variables always exist (do not exist). 相似文献
125.
126.
Sérgio L. C. Ferreira Marcus L. S. F. Bandeira Valfredo A. Lemos Hilda C. dos Santos A. C. Spinola Costa Djane S. de Jesus 《Analytical and bioanalytical chemistry》1997,357(8):1174-1178
A simple and very sensitive method has been developed for the determination of ascorbic acid based on the oxidation of ascorbic
acid to dehydroascorbic acid by iron(III), followed by a complexation of iron(II) with 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol(Br-PADAP).
The iron(II) complex is formed immediately, with absorption maxima at 560 and 748 nm and a molar absorptivity of 1.31 × 105 l mole–1cm–1 and 5.69 × 104 l mole–1cm–1, respectively. The ascorbic acid determination is possible with a linear range up to 2.4 μg ml–1, a calibration sensitivity of 0.744 ml μg–1 at 560 nm and 0.323 ml μg–1 at 748 nm, and a detection limit of 15 ng ml–1 and 44 ng ml–1, respectively. The procedure was used for the ascorbic acid determination in several fruit juices and pharmaceutical formulations.
The results demonstrated a good precision (R.S.D. < 1%) and are in agreement with those obtained with others methods. The
Br-PADAP method proposed is six times more sensitive than the method using the iron(II)-1,10-phenanthroline system.
Received: 7 May 1996 / Revised: 1 July 1996 / Accepted: 8 August 1996 相似文献
127.
Amélia Santos M Gama S Gano L Cantinho G Farkas E 《Dalton transactions (Cambridge, England : 2003)》2004,(21):3772-3781
A new bis(3-hydroxy-4-pyridinone) derivative of iminodiacetic acid, imino-bis(acetyl(1-(3'-aminopropyl)-3-hydroxy-2-methyl-4-pyridinone)), IDAPr(3,4-HP)(2), has been prepared and studied in its interaction with a set of hard metal ions. This tetradentate ligand presents a much higher chelating efficiency for trivalent hard metal ions (Fe, Ga, Al) than the monodentate derivative Deferriprone, namely at the diluted conditions prevailing in physiological conditions and at low clinical doses. A similar behaviour was also observed for the complexation with Zn(II) but at a significantly lower extent. This compound presents a moderate hydrophilic character at physiological pH (logD=-1.72). In vivo assays showed much more rapid clearance of (67)Ga from most tissues of metal-loaded mice than the drug Deferriprone and the radioactivity excretion occurs mostly through the kidneys. Therefore, results from in vitro and in vivo studies indicated good perspectives for this compound to be a potential decorporating agent for hard metal ions in overload situations without depletion of essential metal ions such as zinc. 相似文献
128.
Denilson S.S. dos Santos Alete P. Teixeira José T.P. Barbosa Sérgio L.C. Ferreira Maria das Graças A. Korn Leonardo S.G. Teixeira 《Spectrochimica Acta Part B: Atomic Spectroscopy》2007
In this work, the use of cetyltrimethylammonium bromide as surfactant for the preparation of oil-in-water emulsions for the determination of Cu and Cr in gasoline by electrothermal atomic absorption spectrometry (ET AAS) was evaluated. The surfactant amount was tested in the range of 25 to 300 mg, added to 2 ml of gasoline, and completed to 10 mL with 0.1% (v/v) nitric acid solution. 150 mg of surfactant was found optimum, and a sonication time of 10 min sufficient to form an oil-in-water emulsion that was stable for several hours. The ET AAS temperature program was established based on pyrolysis and atomization curves. The pyrolysis temperatures were set at 700 and 1300 °C for Cu and Cr, respectively and the selected atomization temperatures were 2400 and 2500 °C. The time and temperature of the drying stage and the atomization time were experimentally tested to provide optimum conditions. The limits of detection were found to be 5 μg L− 1 and 1.5 μg L− 1 for Cu and Cr, respectively in the original gasoline samples. The relative standard deviation (RSD) ranged from 4 to 9% in oil-in-water emulsions spiked with 5 μg L− 1 and 15 μg L− 1 of each metal, respectively. Recoveries varied from 90 to 98%. The accuracy of the proposed method was tested by an alternate procedure using complete evaporation of the gasoline sample. The method was adequate for the determination of Cu and Cr in gasoline samples collected from different gas stations in Salvador, BA, Brazil. 相似文献
129.
Inverse gas chromatography (IGC) has been used to study the Lewis acid-base properties of a technologically and commercially important core-shell type elastomer (MBS rubber). The parameters determined were the dispersive component of the surface tension, the surface free energy, the enthalpy and the entropy of adsorption of polar and apolar probes, the surface Lewis acidity constant (Ka), and the surface Lewis basicity constant (Kb). The results show that the MBS rubber is amphoteric but strongly Lewis basic. It is weakly Lewis acidic. The results are in accord with the analysis of the molecular structure of PMMA, the shell component of this impact modifier (IM). The interactivity of this elastomer with the remaining materials in multicomponent polymeric systems is expected to be strongly influenced by the particular surface energetic properties of the MBS rubber. The results presented would contribute to the interpretation, forecast and optimization of the adhesion properties and phase preferences shown by this impact modifier when incorporated in such complex polymeric systems as polymer blends and composites. 相似文献
130.
Sarrión MN Santos FJ Galceran MT 《Rapid communications in mass spectrometry : RCM》2000,14(23):2271-2281
Headspace solid-phase microextraction combined with gas chromatography/ion trap tandem mass spectrometry (HS-SPME/GC/ITMS/MS) was used for the analysis of 12 halobenzenes from soil samples. For MS/MS optimisation, the experiments were performed by precursor ion selection and software controlled operations. Collision-induced dissociation (CID) can be achieved by two different approaches, resonant and non-resonant excitation modes. Different results were obtained using the two approaches, and the resonant excitation mode was chosen as the best for all halobenzenes. Parameters such as the CID excitation amplitude, excitation RF storage level and CID bandwidth frequency were optimised to maximise the formation of halobenzene product ions. A 100-microm polydimethylsiloxane fibre was used for the isolation and preconcentration of the analytes. The HS-SPME/GC/ITMS/MS method was applied to the analysis of halobenzenes in an agricultural soil sample. The halobenzenes were quantified by standard addition, which led to good reproducibility (RSD between 4.7 and 9.2%) and detection limits in the low pg/g range. The method was validated by comparing the results with those obtained in a European inter-laboratory exercise. 相似文献