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51.
We investigate the tail behavior of the sojourn-time distribution for a request of a given length in an M/G/1 Processor-Sharing (PS) queue. An exponential asymptote is proven for general service times in two special cases: when the traffic load is sufficiently high and when the request length is sufficiently small. Furthermore, using the branching process technique we derive exact asymptotics of exponential type for the sojourn time in the M/M/1 queue. We obtain an equation for the asymptotic decay rate and an exact expression for the asymptotic constant. The decay rate is studied in detail and is compared to other service disciplines. Finally, using numerical methods, we investigate the accuracy of the exponential asymptote. AMS 2000 Subject Classifications Primary:60K25,Secondary: 60F10,68M20,90B22  相似文献   
52.
An all-fiber 1.48-mum generator based on a laser-diode-pumped Yb-doped double-clad laser and a cascaded Raman wavelength converter has been developed. Second-order Raman Stokes radiation was generated in a phosphosilicate-fiber resonator formed by two pairs of Bragg gratings. A slope efficiency of the Raman converter of 48% with respect to the power emitted by the double-clad Yb laser has been achieved. We obtained an output power of 1 W at a slope efficiency of 34% with respect to the laser-diode array power, with a total optical-to-optical efficiency of 23%.  相似文献   
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Interfacial interactions and dynamics were studied in silica and alumina core-poly(vinyl pyrrolidone) (PVP) shell nanoparticles with different shell thicknesses starting from 1-2 nm (monolayer); their geometry and structural organization were comprehensively characterized by several techniques. Far- and mid-IR spectroscopy, combined with DSC activation analysis of the glass transition, allowed to register hydrogen bonding and Lewis/Brønsted interactions, and the multi-modal glass transition dynamics in PVP nanoshells, as well as their interrelationship. For PVP monolayer, only a few “abnormal” modes constituted glass transition which covered the temperature range from 80 to 230 °C, with varying the activation energy by an order of magnitude.  相似文献   
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The results of a study on the activity and operational stability of an Au–Pd/MFI/Al2O3 catalyst in the reaction of ethanol conversion into a gasoline fraction of hydrocarbons are reported. In the presence of the Au–Pd/MFI/Al2O3 catalyst, ethanol was almost completely converted into an alkane–aromatic fraction of C3–C11 hydrocarbons at 300°C in an atmosphere of Ar; the yield of this fraction was as high as 90% on a feed carbon basis. It was established that, in the presence of the bimetallic Au–Pd catalyst, the yield of the target fraction increased by 10%, as compared with that on a monometallic Au-containing sample. The Au–Pd/MFI/Al2O3 catalyst exhibited much higher stability in a long-term experiment in comparison with the previously tested pilot sample of Pd–Zn/MFI/Al2O3. After a 40-h operation, the yield of the target fraction of C3+ hydrocarbons in the presence of the Au–Pd/MFI/Al2O3 catalyst decreased by 15%. The treatment of the catalyst with hydrogen led to the complete restoration of its activity. The structure of the Au–Pd active constituents was studied by transmission electron microscopy X-ray photoelectron spectroscopy. methods of the and microscopy.  相似文献   
58.
Pentaphenylantimony and -phosphorus react with arylmercury chlorides in toluene at room temperature to give diaryl derivatives of mercury in yields of up to 95%. The reactions of pentaphenylantimony and -phosphorus with silicon and tin halides involve arylation of the latter in yields of up to 79%. The products of the reaction of pentaphenylphosphorus with triphenylbismuth dihalides are tetraphenylphosphorus halides, triphenylbismuth, and halobenzene.  相似文献   
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The standard enthalpies of formation of uranophosphates MI I(PUO6)2·nH2O (MI I = Mn, Fe, Co, Ni, Cu, Zn, Cd) are determined. The standard enthalpies of the synthesis and dehydration of these compounds are calculated and analyzed.  相似文献   
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Spiropyrrolidine derivatives were synthesized for the first time by [3+2]-cycloaddition of 3-arylmethylene-3H-furan(pyrrol)-2-ones to N-benzylidenebenzylamine activated by the system AcOAg-Et3N. The reaction route and the spectral characteristics of the first obtained compounds have been discussed.  相似文献   
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