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971.
Techniques of uniformization are used to prove that it is not consistent that the Whitehead groups of cardinality ℵ1 are exactly the strongly ℵ1-free groups. Some consequences of the assumption that every strongly ℵ1-free group of cardinality ℵ1 is Whitehead are derived. Other results about uniformization are also proved.
Research partially supported by NSERC grant #9848.
Research partially supported by the BSF. The authors thank Rutgers University for its support. Publication #441. 相似文献
972.
973.
974.
Christian R. Noe M. Knollmüller K. Dungler C. Miculka P. Gärtner 《Monatshefte für Chemie / Chemical Monthly》1991,122(8-9):705-718
Summary Acetals3 and4 of alkylthienylcarbinols1 were prepared using an enantiomerically pure lactol2. In the key step these compounds were desulfurized. After deprotection the target compounds7 andent-7 were obtained.
Herrn Prof. Dr. H. Oelschläger zum 70. Geburtstag gewidmet 相似文献
975.
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
976.
Magnetization reversal processes by a switching field in single-domain nano-sized magnetic particles in the presence of a small transverse non-static bias field are studied. Applying an oscillating bias field instead of a static field, the reversal time becomes much shorter when the switching field is slightly stronger than the effective anisotropy field. A pulsed bias field of a suitably chosen duration in the nanosecond scale is found to induce a rapid switching, even when the switching field is smaller than the anisotropy field. The dependence of the reversal time on the frequency of an oscillating bias field and the duration of a pulsed bias field are studied. The present work thus complement the earlier studies on switching in the presence of a static bias field. 相似文献
977.
Marilyn M. Olmstead James C. Fettinger Soya Gamsey Jacob W. Clary Bakthan Singaram 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(6):o333-o335
The structures of three chiral vinyldioxazaborocanes are reported, namely (2E)‐ and (2Z)‐6‐benzyl‐2‐buten‐2‐yl‐1,3,6,2‐dioxazaborocane, C27H30BNO2, (II) and (III), respectively, and (2Z)‐2‐buten‐2‐yl‐6‐isobutyl‐1,3,6,2‐dioxazaborocane, C24H32BNO2, (IV). These compounds may be useful in asymmetric reactions. In the structures reported here, the N—B donor–acceptor bond is longer than in any previously reported analogous compounds. 相似文献
978.
The electrocatalytic oxidation of 2-propanol was investigated using on line differential electrochemical mass spectrometry (DEMS) on electrodeposited Pt and an arrange of bimetallics: Pt0.84Rh0.16, Pt0.70Rh0.30, Pt0.55Rh0.45. It has been observed that the Pt0.84Rh0.16 bimetallic electrode presented the best catalytic activity for 2-propanol electrochemical oxidation. Since 2-propanol is a secondary alcohol, only acetone and CO2 are produced. The total yield of CO2 and acetone has been determined from the DEMS measurements. It is found that acetone is the major product, as reported before for other electrodes. The acetone and CO2 yield depends on the electrode composition. High amount of rhodium in the electrode composition strongly diminish the reaction rate as indicated by the decrease of both the acetone and CO2 yield. However, acetone inhibition is much more intense. The only bimetallic electrode that presents considerable mass spectroscopy signals intensity for CO2 and acetone is the Pt0.84Rh0.16 electrode. This electrode shows a slight increase in CO2 selectivity, compared to the other electrodes studied in this work. Only very low coverages of stable adsorbates were present during the reaction. Two and one carbon adsorbate were observed for all the electrodes. Three carbon adsorbates were detected only for the Pt0.84Rh0.16 electrode. Therefore, acetone production does not require a stable adsorbate. 相似文献
979.
K. Adu-Wusu N. M. Hassan C. A. Nash J. C. Marra 《Journal of Radioanalytical and Nuclear Chemistry》2006,267(2):381-388
Summary The removal of cesium from aqueous waste solution was investigated in a column setup using a relatively coarse SuperLigò644 resin. The bed volume (BV=140) at the onset of breakthrough surpassed the design requirement of 100 BV at 50% breakthrough,
and also corresponds to 99.96% cesium removal. Cesium elution with 0.5M HNO3was satisfactory with a peak BV of 2.5. The elution BV for C/C0=0.01 was 10, which is less than the target of 15 BV. The percent of sorbed cesium eluted was 99.88%. Further, the BV of the
various solutions used for the supporting process steps was sufficient. 相似文献
980.
We present a review of our recent measurements of total cross sections (Q
T's) for the scattering of positrons by Na, K, and Rb, and positronium-formation cross sections (Q
Ps's) for Na and K. For our total cross section measurements, a beam transmission technique has been used. For ourQ
Ps measurements, our approach involves setting upper and lower limits onQ
Ps using a combination of (1) measuring the transmission of the positron beam with the angular discrimination of the apparatus made as poor as possible, and (2) measuring the 511 keV annihilation gamma rays in coincidence produced by the decay of para-Ps formed in the scattering cell. Comparison with theoretical calculations shows that our measuredQ
T's andQ
Ps's for Na and K agree reasonably well with a close coupling approximation (CCA) calculation which takes into account the formation of Ps in then=1 andn=2 states. In the 3–10 eV energy range, this calculation predicts a peak in theQ
T's andQ
Ps's for K which also appears in our measurements. The absence of such a peak in our measuredQ
T's andQ
Ps's (preliminary) for Na in this energy range is also consistent with the same theory. Comparisons with five-state CCA calculations ofQ
T which do not take Ps-formation into account also show good agreement with our positron-Na, K, and RbQ
T measurements for energies above 20 eV, but show dramatic departures from our measurements below 10 eV for K and Rb. 相似文献