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991.
Strontium has been determined in a human serum reference material by ICP-MS and by NAA. By ICP-MS, results for (88)Sr and (86)Sr in both 10- and 5-fold diluted serum were in good agreement. For (88)Sr the precision was better than 3% and the detection limit was 0.05 mug/l. under the conditions used. The results were 25.5 mug/l. in the liquid serum or 0.281 mug/g in the lyophilized reference material. In the NAA the (87m)Sr produced was radiochemically separated by extraction with oxine in chloroform. The precision was about 10% and the detection limit 0.02-0.05 mug/g.  相似文献   
992.
The use and limitations of the microcomputer as an aid for the analyst in the identification of powdered vegetable materials is presented and suggestions are given for extending the applicability of the method and the programs described.  相似文献   
993.
Reaction of phenyl N-(8-quinolinyl)carbamate with sodium borohydride afforded 1,2-dihydro-4H-imidazo-[5,4,1-ij]quinolin-2-one, 2a . The 5,6-double bond of 2a was functionalized by reaction with nitrosyl chloride to give the nitroolefin 4 and by reaction with hypobromous acid to give the trans-bromohydrin 5 . Reaction of 5 with sodium azide led to the rearranged trans-6-azido-5-ol 7 , the structure of which was determined by 1H nmr studies.  相似文献   
994.
On the Structure of Ill-crystallized Calcium Hydrogen Silicates. II. A Phase Consisting of Poly and Disilicate Both by condensation reactions of a calcium hydrogen disilicate phase [1] under the mother liquid at 80°C and by hydrothermal reactions of lime and silica at 150°C an ill-crystallized calcium hydrogen silicate phase is formed, being built up by nearly equal parts (referred to Si) of poly-and disilicate anions. The CaO content of the phase synthesized at 80°C varies between 1.1 and 2CaO/SiO2, depending on the Ca(OH)2 concentration in the mother liquid. In the phase formed at 150°C is CaO/SiO2 = l.l–l.5. A proposal for the constitution of this phase is given.  相似文献   
995.
Standard explosives and technical mixtures of explosives have been investigated by field desorption mass spectrometry. The compounds investigated gave intense molecular ions or protonated molecules and structurally significant fragmentation. For comparison, the corresponding electron impact and chemical ionization mass spectrometry data are reported. Emission-controlled field desorption, photographic detection, and accurate mass measurements enabled the components of the technical mixtures to be identified. An example of the determination of an additive in a technical product by field desorption mass spectrometry and stable isotope dilution is given. The use of these techniques for quality control of explosives and for forensic investigations appears to be promising.  相似文献   
996.
The separation of racemic benoxaprofen into the two benoxaprofen enantiomers by preparative high-performance liquid chromatography and the application of the activated enantiomers as derivatization reagents for the simultaneous stereoselective determination of chiral amines in biological material is described. Activated (+)- and (-)-benoxaprofen are both shown to be very sensitive and stable chiral fluorescence markers, applicable to thin-layer chromatography as well as to high-performance liquid chromatography.  相似文献   
997.
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1000.
We investigate the dynamics of one anisotropic spin in an external time-dependent magnetic field. The classical dynamics of the system is nonintegrable (and very similar to the standard map). We present results on this model for a quantum spin (i.e. for finite values of the spin lengthS). In particular we discuss the semiclassical regime,S1, using the concept of Wigner functions to define a suitable probability distribution. In regular regions of phase space the time evolution of the probability distribution shows an algebraic decay of correlations as in quantum mechanics. In chaotic regions of phase space it is characterised by a positive Lyapunov exponent which depends onS. In these regions semiclassical trajectories coincide with classical ones fort <0 where 0InS.  相似文献   
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