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141.
142.
InP/InGaAs multiple quantum well structures with up to 200 periods have been grown by CBE. These structures exhibit exceptional lateral uniformity, measured as ±1 Å in period, ±13 ppm in lattice mismatch and ±0.5 nm in wavelength across a 2 inch wafer. Good surface morphology, sharp interfaces and excellent growth control have all been demonstrated.  相似文献   
143.
Biosynthetic human growth hormone specifically 13C-labelled in the carbonyl positions of all 26 leucine residues has been obtained by recombinant DNA techniques using 13C-labelled leucine and an E. coli strain that requires leucine. It is shown that, on the whole, the labelling is specific with no significant mislabelling as would have been the case had the 13C-labelled leucine been metabolized.  相似文献   
144.
Particle motion in the SU(2) manifold is quantized by path integrals. It is shown that the Poschl-Teller, Wood-Saxon, and Rosen-Morse potentials are solved by relating their propagators to the path integrations over the SU(2) manifold. Examples with some other groups are mentioned.  相似文献   
145.
A 480 L evacuable reaction chamber, equipped with FT-IR spectroscopy on-line and ion chromatography off-line, has been used to study the gas phase reaction between the nitrate radical, NO3, and the reduced organic sulphur compounds CH3CH2SH, (CH3CH2)2S, (CH3CH2)2S2, and CH3CH2SCH3 in air. The products CH3CH2SO3H, SO2, H2SO4, CH3CHO, and CH3CH2ONO2 were identified and quantified in the reactions of the first three compounds, CH3CH2SH, (CH3CH2)2S, and (CH3CH2)2S2. The reaction products were CH3CH2SO3H, CH3SO3H, SO2, H2SO4, CH3CHO, and CH2O in the reaction of CH3CH2SCH3. On the basis of identified reaction products and intermediates observed in the infrared spectra, mechanisms are proposed for the reactions between the NO3 radical and the four reduced organic sulphur compounds. The results of this study, together with those from previous experiments performed in this laboratory on CH3SCH3, CH3SH, and CH3SSCH3 lead to the conclusion that all these species, in the reaction with the NO3 radical, follow a similar degradation mechanism producing SO2, H2SO4, R? SO3H, R? CHO, and R? CH2ONO2, as the main reaction products. The inital step of the reaction of NO3 with R? S? R and R? S? H type (R = CH3, CH2CH3) reduced organic sulphur compounds was found to be H-atom abstraction, probably after the formation of an initial adduct. For the reaction between NO3 and R? S? S? R type compounds, evidence for an addition-decomposition reaction, as the initial steps, was obtained. R? S·, R? S(O)·, and R? S(O)2· appear to be formed as intermediates in all the reactions. © John Wiley & Sons, Inc.  相似文献   
146.
Summary Four different bottled water brands sold in Greece in the winter of 2001-2002 were analyzed for a wide range of chemical elements, using neutron activation analysis (NAA). The elements Na and Br were determined instrumentally (INAA), whereas the other metals and trace elements radiochemically (RNAA). The results indicated that the mean level of all the elements determined in the samples were well within the European Union (EU) directive on drinking water and accomplish the drinking water standards of the World Health Organisation (WHO) as well as of the Food and Drug Administration (FDA).  相似文献   
147.
148.
The application, the advantage and limits of neutron monitoring techniques, such as Hf-monitors, fissile material accumulation and concentration monitors are being discussed. The active neutron counting technique applied to emptied pulsed extraction columns containing Hf-sieve plates allows conclusive answers as to the position of the plates in the columns. Pu-accumulations on Hf-sieve plates in pulsed extraction columns can be estimated within a factor of two, whereby the detection limit is about equal to or less than 1 g Pu/plate. Fissile material concentration changes of 1.1 g/l can be detected in the case of235U in solution and of 0.4 Pu/l if a239Pu/240Pu ratio of 4 to 1 is assumed.  相似文献   
149.
150.
Polarized absorption and emission spectra, and temperature dependences of the fluorescence lifetimes and intensities for the chromium-doped LiNbGeO5 laser crystal are presented. Crystal symmetry and comparison with the infrared fluorescence properties of the Cr-doped Mg2SiO4 and Y3Al5O12 laser crystals seem to identify the active center as a Cr4+ ion in a tetrahedral site.  相似文献   
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