Measurement of the Lambda0b lifetime in the decay lambda0b--> J/psiLambda0 with the D0 detector

We present measurements of the Lambda(0)(b) lifetime in the exclusive decay channel Lambda(0)(b)--> J/psiLambda(0), with J/psi--> mu(+)mu(-) and Lambda(0)--> ppi(-), the B0 lifetime in the decay B0-->J/psiK(0)(S) with J/psi--> mu(+)mu(-) and K(0)(S)-->pi(+)pi(-), and the ratio of these lifetimes. The analysis is based on approximately 250 pb(-1) of data recorded with the D0 detector in pp collisions at sqrt[s] = 1.96 TeV. The Lambda(0)(b) lifetime is determined to be tau(Lambda(0)(b)) = 1.22(+0.22)(-0.18)(stat) +/- 0.04(syst) ps, the B0 lifetime tau(B0) = 1.40(+0.11)(-0.10)(stat) +/- 0.03(syst) ps, and the ratio tau(Lambda(0)(b))/tau(B0) = 0.87(+0.17)(-0.14)(stat) +/- 0.03(syst). In contrast with previous measurements using semileptonic decays, this is the first determination of the Lambda(0)(b) lifetime based on a fully reconstructed decay channel.     

An unconventional method for measuring the Tc L3‐edge of technetium compounds

Tc L₃‐edge XANES spectra have been collected on powder samples of SrTcO₃ (octahedral Tc⁴⁺) and NH₄TcO₄ (tetrahedral Tc⁷⁺) immobilized in an epoxy resin. Features in the Tc L₃‐edge XANES spectra are compared with the pre‐edge feature of the Tc K‐edge as well as other 4d transition metal L₃‐edges. Evidence of crystal field splitting is obvious in the Tc L₃‐edge, which is sensitive to the coordination number and oxidation state of the Tc cation. The Tc L₃ absorption edge energy difference between SrTcO₃ (Tc⁴⁺) and NH₄TcO₄ (Tc⁷⁺) shows that the energy shift at the Tc L₃‐edge is an effective tool for studying changes in the oxidation states of technetium compounds. The Tc L₃‐edge spectra are compared with those obtained from Mo and Ru oxide standards with various oxidation states and coordination environments. Most importantly, fitting the Tc L₃‐edge to component peaks can provide direct evidence of crystal field splitting that cannot be obtained from the Tc K‐edge.     

The Effect of Platinum on Diffusion Kinetics in β‐NiAl: Implications for Thermal Barrier Coating Lifetimes

Platinum is added to thermal barrier coatings (TBCs) as it is observed empirically to extend their lifetime, but the mechanism by which Pt acts is unknown. Since Pt has been proposed to alter diffusivities in NiAl, a key component of TBCs, we use first‐principles quantum mechanics calculations to investigate atomic level diffusion mechanisms. Here, we examine the effect of Pt on five previously proposed mechanisms for Ni diffusion in NiAl: next‐nearest‐neighbor jumps, the triple defect mechanism, and three variants of the six jump cycle. We predict that Pt increases the rate of Ni diffusion by stabilizing point defects and defect clusters that are diffusion intermediates. Previously, we predicted the triple defect mechanism to be a dominant Ni diffusion mechanism; it simultaneously results in long‐range Al diffusion in the opposite direction. Since Pt increases the rate of Ni diffusion, it also increases Al diffusion in NiAl, which may be key to extending the coating lifetime.     

Evidence of upward spread of suppression in DPOAE measurements

Measurements of DPOAE level in the presence of a suppressor were used to describe a pattern that is qualitatively similar to population studies in the auditory nerve and to behavioral studies of upward spread of masking. DPOAEs were measured in the presence of a suppressor (f3) fixed at either 2.1 or 4.2 kHz, and set to each of seven levels (L3) from 20 to 80 dB SPL. In the presence of a fixed f3 and L3 combination, f2 was varied from about 1 oct below to at least 1/2 oct above f3, while L2 was set to each of 6 values (20-70 dB SPL). L1 was set according to the equation L1 = 0.4L2 + 39 [Janssen et al., J. Acoust. Soc. Am. 103, 3418-3430 (1998)]. At each L2, L1 combination, DPOAE level was measured in a control condition in which no suppressor was presented. Data were converted into decrements (the amount of suppression, in dB) by subtracting the DPOAE level in the presence of each suppressor from the DPOAE level in the corresponding control condition. Plots of DPOAE decrements as a function of f2 showed maximum suppression when f2 approximately = f3. As L3 increased, the suppressive effect spread more towards higher f2 frequencies, with less spread towards lower frequencies relative to f3. DPOAE decrement versus L3 functions had steeper slopes when f2 > f3, compared to the slopes when f2 < f3. These data are consistent with other findings that have shown that response growth for a characteristic place (CP) or frequency (CF) depends on the relation between CP or CF and driver frequency, with steeper slopes when driver frequency is less than CF and shallower slopes when driver frequency is greater than CF. For a fixed amount of suppression (3 dB), L3 and L2 varied nearly linearly for conditions in which f3 approximately = f2, but grew more rapidly for conditions in which f3 < f2, reflecting the basal spread of excitation to the suppressor. The present data are similar in form to the results observed in population studies from the auditory nerve of lower animals and in behavioral masking studies in humans.     

Order-parameter and the discontinuous antiferro-paramagnetic transition in manganese oxide

Studies of monodomain manganese oxide by neutron diffraction and strain gauge measurements show that the antiferro-paramagnetic transition is clearly discontinuous. At the transition the order-parameter drops by about 60 percent of the T = 0 K value.     

The magnetic properties of FexCo1-x and FexTi1-x alloys

High pressures and high magnetic field behaviour give indications on the nature of magnetism encountered in transition metal alloys. We present experiments performed under pressure up to 7 kbar, in fields up to 150 kOe, between 1.4 K and 300 K. The results are used to discuss the occurence of ferromagnetism in Fe_xCo_10xSi and Fe_xCo_1-xTi systems. These systems exhibit two critical concentrations for the onset of ferromagnetism. Their magnetic properties are very sensitive to magnetic fields and high pressures and this allows us to characterize them as weak itinerant ferromagnets. A more localized behaviour is evidenced for the iron rich alloys and the appearance to ferromagnetism is different for cobalt rich side and for iron rich one.     

The high field-high pressure magnetic properties of MnSi

Experiments at high pressures and magnetic fields indicate that although MnSi is an unsaturated ferromagnet it cannot be characterized as a simple weak itinerant one.