Measurement of the angular distribution of the polarization of the recoil proton from the photoproduction of neutral pions on hydrogen at a photon energy of 360 MeV. II

The angular distribution of the polarization of the recoil protons from the reactionγ+p→π ⁰+p has been measured at a photon energy of 360 MeV and at pion CM angles of 58°, 75°, 96° and 105°. The polarization of the protons has been determined by the left to right ratio in scattering on a helium gas target. The trajectory of each scattered proton has been measured by a system of spark chambers.     

Angular correlation measurements in the Be9(d,p, γ)Be10 reaction

Thep-γ angular correlations in the Be⁹(d, p, γ)Be¹⁰ reaction have been measured in the reaction plane atE _d =1.3, 1.5, 1.9, 2.3 and 2.45 MeV for proton anglesθ _p =35°, 80° and 120°. The anisotropy of the angular correlations measured forθ _p =35° is independent of deuteron energy. A systematic shift of the symmetry axis from the recoil direction has been observed. The shift is 20.5° at E_d=2.45 MeV. The anisotropy decreases with increasing proton angle and vanishes atθ _p =120°.     

Messung der Spinpolarisation langsamer Elektronen nach elastischer Streuung an festen Hg-Targets

SpinpolarizationP(Θ) of slow electrons elastically scattered by a solid Hg-target has been studied in a double-scattering experiment for electron energies between 300 eV and 900 eV. For the same energy range the angular dependence of the scattered intensity has been measured. Maximum degree of polarization found isP=?0.23±0.04 (E=900 eV,Θ=105°).     

Excitation of the Yb II transitions terminating on the low-lying odd levels

Excitation of the transitions from the even levels of a singly charged ytterbium ion that terminate on the low-lying odd levels 4f ¹³(² F°)6s ^{2 2} F°, 4f ¹⁴(¹ S)6p ² P°, and 4f ¹³(² F°_7/2)5d6p(³ D)³[3/2]° is experimentally studied by measuring 51 excitation cross sections at an electron energy of 50 eV, and 16 optical excitation functions are determined within the electron energy range 0–200 eV. The largest magnitudes of the measured cross sections exceed 3 × 10^?17 cm².     

Der Zerfall des Lu176m

The decay of Lu^176m has been investigated. TheK-conversion coefficient α _K of the 88,3 keV niveau of Hf¹⁷⁶ has been determined to α _K =1,35±0,07. Theβ-branching ratio to the 0+ and 2+ niveau of Hf¹⁷⁶ has been measured by means of aβ-γ-coincidental technique. (60,4±6,1)% of Lu^176m decay into the 2+ niveau and (39,6±6,1)% into the 0+ niveau of Hf¹⁷⁶.K-capture of Lu^176m to Yb¹⁷⁶ was not found. If there is any, it is less than 0,1% of all decays.     

Propriétés magnétiques du thulium à l'état de sesquioxyde et de métal entre 0 et 110 kOe et de 2 à 1560°K

Tm₂O₃ obeys between 80 and 980°K the Curie-Weiss lawχA (T+25=7,08) withμ _eff=7.56 Bohr magnetons, the theoretical value for Tm³⁺(J=6,g=7/6). In the behavior of the metal,χΛ(T-14)=7.45 between 80 and 1540°K, a contribution of the non-localized electrons should be considered at high temperatures. The susceptibility of the metal is maximum at 53°K, minimum near 35°K, and the behavior is antiferromagnetic between these two temperatures, ferromagnetic below 35°K. An additional transition occurs near 10°K, vanishing by cooling in a magnetic field. The effect of this cryomagnetic treatment on the magnetization and the remanence has been measured in six different cooling fields. The magnetization reaches 1.0 and 5.0 magnetons in 26.7 and 110 kOe (pulsed field) respectively, whereas the saturation for the ground state³H₆ isgJ=7.     

Transverse polarization of the lepton in the decay process <Emphasis Type="Italic">B</Emphasis> → <Emphasis Type="Italic">Dlν</Emphasis><Subscript>l</Subscript> due to electromagnetic final-state interaction

The emergence of transverse polarization of the lepton in the decay processes B⁰ → D^?l⁺ν_l and \(B^ + \to \bar D^0 l + \nu _l \) for l = τ, μ is studied on the basis of the Standard Model in the leading approximation of heavy-quark effective theory. It is shown that a nonzero transverse polarization appears owing to electromagnetic final-state interactions at the one-loop level. Diagrams involving D and D* mesons in the intermediate state and making a nonzero contribution to the transverse polarization of the outgoing lepton are considered. If only these mesons are taken into account in evaluating the mean values of the τ-lepton polarization in the decays B⁰→D^?τ⁺ν_τ and \(B^ + \to \bar D^0 \tau ^ + \nu _\tau \), the results are 2.60×10^-3 and ?1.59×10^?3, respectively. The corresponding values of the transverse muon polarization averaged over the Dalitz plot are 2.97×10^?4 and-6.79×10^?4.     

Paramagnetische Relaxation im Terbiumäthylsulfat

The paramagnetic relaxation of Tb_0,01 Y_0,99(C₂H₅SO₄)₃·9H₂O at temperatures between 1,14°K and 4,21°K has been investigated with the absorption-dispersion method at frequencies between 5 sec^?1 and 10240 sec^?1 and different magnetic fields. AtH=700 Oe. The relaxation time follows the equationτ ^?1=[A H ³ coth (g _z μ _B H/2k T)+B T ⁷] sec^?1 as a function of temperature. ForH<800 Oe the paramagnetic relaxation is influenced by cross relaxation processes between the hyperfine structure levels.     

Zur Konzentrationsabhängigkeit der Elektronenspin-Relaxationszeiten von Diphenyl-Picryl-Hydrazyl in fester Phase

The influence of exchange and dipol interaction on the EPR-relaxation timesT ₁ andT ₂ of DPPH has been measured in theX-band between 295 and 2°K. The spinconcentration has been varied between 1.5·10²¹ spins/cm³ (single crystals) and 1.5·10¹⁸ spins/cm³ (solid solution in polystyrene). The EPR absorption was saturated stationarily. This gave the productT ₁ T ₂ from the saturation curve and the timeT ₂ from saturation broadening of the absorption spectrum.     

Zeitliches Abklingen und Anisotropie von p-Terphenyl- undp-Terphenyl-Anthrazen-Mischkristallen bei Beschuß mit α-Teilchen

The time dependence of scintillation intensity from single crystals ofp-terphenyl and mixed crystals ofp-terphenyl and anthracene after bombarding with α-particles was investigated at the two temperaturesT=296 °K andT=92 °K. For the crystals ofp-terphenyl the time dependence of the scintillation anisotropy was also measured. Using the formulas given byKing andVoltz the decay curves ofp-terphenyl were decomposed into two components. Good agreement between experiment and theory was found. The ratio of the prompt intensity to the delayed intensity was determined to be 1∶2 atT=296 °K and 1∶3 atT=92 °K. The diffusion constants for triplet excitons were calculated to beD _T(296 °K)≈10^?5 cm² sec^?1 andD _T(92 °K)≈ 2×10^?6 cm² sec^?1, and the triplet-triplet interaction rate constantsχ _tt(296 °K)≈ 2.5×10^?11 cm³ sec^?1 andχ _tt(92 °K)≈0.5×10^?11 cm³ sec^?1.     

Thermal conductivity of partially graphitized biocarbon obtained by carbonization of medium-density fiberboard in the presence of a Ni-based catalyst

The thermal conductivity k and resistivity ρ of biocarbon matrices, prepared by carbonizing medium-density fiberboard at T _carb = 850 and 1500°C in the presence of a Ni-based catalyst (samples MDF-C( Ni)) and without a catalyst (samples MDF-C), have been measured for the first time in the temperature range of 5–300 K. X-ray diffraction analysis has revealed that the bulk graphite phase arises only at T _carb = 1500°C. It has been shown that the temperature dependences of the thermal conductivity of samples MDFC- 850 and MDF-C-850(Ni) in the range of 80–300 K are to each other and follow the law of k(T) ～ T ^1.65, but the use of the Ni-catalyst leads to an increase in the thermal conductivity by a factor of approximately 1.5, due to the formation of a greater fraction of the nanocrystalline phase in the presence of the Ni-catalyst at T _carb = 850°C. In biocarbon MDF-C-1500 prepared without a catalyst, the dependence is k(T) ～ T ^1.65, and it is controlled by the nanocrystalline phase. In MDF-C-1500(Ni), the bulk graphite phase formed increases the thermal conductivity by a factor of 1.5–2 compared to the thermal conductivity of MDF-C-1500 in the entire temperature range of 5–300 K; k(T = 300 K) reaches the values of ～10 W m^–1 K^–1, characteristic of biocarbon obtained without a catalyst only at high temperatures of T _carb = 2400°C. It has been shown that MDF-C-1500(Ni) in the temperature range of 40?300 K is characterized by the dependence, k(T) ～ T ^1.3, which can be described in terms of the model of partially graphitized biocarbon as a composite of an amorphous matrix with spherical inclusions of the graphite phase.     

Calculation of the polarization of the recoil proton in πN-scattering near the inelastic threshold

The polarization of the recoil proton in πN-scattering has been calculated as a function of the scattering angle at the energies 150, 170, 190 MeV. It is shown that this polarization depends sensitively on the πN-scattering phase-shiftP ₁₁. Slight changes of the other phase-shifts do not affect the polarization to the same extent. New measurements of the differential cross-section and of the polarization in the process π^?+p→π^?+p are suggested. They would allow for a new precise phase-shift analysis, which could possibly determine the sign of theP ₁₁-phase at the inelastic threshold. This sign is important in connection with the bound-state picture of the nucleon.     

Observation of high efficiency of Raman scattering in the process of the three-photon ionization of samarium atom

Very high efficiency of Raman scattering on samarium atoms in the process of three-photon ionization has been detected. An intense maximum attributed to the one-photon transition 4f ⁶5d6s ⁹ H ₂ → 4f ⁵5d6s ^{2 7} D ₃° between two excited states is observed in the dependence of the yield of Sm⁺ ions on the laser-radiation frequency. The 4f ⁶5d6s ⁹ H ₂ state is populated owing to the spontaneous Raman scattering 4f ⁶6s ^{2 7} F ₃ + ω ? ν → 4f ⁶5d6s ⁹ H ₂.     

Manifestation of the Coster-Kronig effect in the near-threshold electron-impact excitation of the Cd<Superscript>+</Superscript> ion

The near-threshold portions of the energy dependences of the effective excitation cross sections of the resonance transition 4d¹⁰5p²P_1/2° → 4d¹⁰5s²S_1/2 and the two-electron forbidden transition 4d⁹5s²²D_5/2 → 4d¹⁰5p²P_3/2° in the spectrum of the Cd⁺ ion were investigated by the spectroscopic method in crossed electron and ion beams. In the region of energy splitting of the ²P° and ²D levels, a significant resonance contribution of the autoionizing states of cadmium (decaying during the Coster-Kronig process) to the effective excitation cross sections of the noted transitions was revealed for the first time. It is found that the resonance contribution manifests itself much more strongly for the forbidden transition in comparison with the more intense resonance transition; i.e., the manifestation of the Coster-Kronig effect in the electron excitation of ions depends strongly on the cross section of the direct process. It is ascertained that, during the Coster-Kronig process, the main contribution to the resonance excitation of both the resonance and the two-electron forbidden spectral transitions is from the low-lying terms of the series of autoionizing states 4d¹⁰5p(²P_3/2°)ns, md and 4d⁹(²D_3/2)5s²ns, md, which are in the splitting region of the ²P_{1/2, 3/2}° and ²D_{5/2, 3/2} levels, rather than from the high-lying atomic autoionizing states of cadmium, which are located near the ionization limits (corresponding to the and ²P_3/2° and ²D_3/2 levels).     

Precision measurement of the rate of nuclear muon capture in the muonic hydrogen atom and the determination of the pseudoscalar form factor of the nucleon

The rate Λ _S of nuclear muon capture by a proton from the hyperfine singlet ground state of the µp atom has been measured using a new experimental method based on a time-projection chamber operating in an ultrapure hydrogen gas at a pressure of 10 atm. The capture rate has been determined from the difference between the measured lifetime of the negative muon in hydrogen and the world average lifetime of the positive muon. The analysis of 10% of the collected statistics (2 × 10¹⁰) of µe decays yields the muon capture rate Λ _S = 725.0 ± 17.4 s^?1, from which the pseudoscalar form factor of the nucleon, g _P (q _c ² = ?0.88m _µ ² ) = 7.3 ± 1.1, is determined. The further analysis of the collected experimental data should improve the precision of this measurement by a factor of 3.     

Heat capacity and thermodynamic properties of HoMnO<Subscript>3</Subscript> in the range of 364–1046 K

The temperature dependence of the molar heat capacity of HoMnO₃ has been measured by differential scanning calorimetry. The experimental data have been used to calculate the thermodynamic properties of the oxide compound (changes in the enthalpy H°(T)–H°(364 K), entropy S°(T)–S°(364 K), and reduced Gibbs energy Φ°(T)). The data on the heat capacity of HoMnO₃ have been generalized in the range of 40–1000 K.     

M-Zentrenbildung in röntgenbestrahltem KCl

The equilibrium betweenF- andM-center concentration in KCl after X-irradiation at temperatures between 77 °K and 298 °K has been studied. At low temperatures (<200 °K) onlyF-centers which are formed statistically as nearest neighbours give aM-center. At higher temperaturesF-centers within a certain sphere of interaction with a radiusr formM-centers. The temperature dependance of this radiusr has been evaluated. The equilibrium constantK depends on the temperature in the form K=K₀exp(-Q/kT). The activation energy was determined to be Q=(0.5±0.1) eV.     

M-Zentrenbildung in röntgenbestrahlten KCl-Kristallen

The production of F- and M-centres in KCl by X-irradiation has been studied at temperatures between ?20 °C and 50 °C. The optical absorption measurements could be conducted without interrupting the X-irradiation. The results can be summarized as follows: 1. In Harshaw KCl crystals the number of F-centres created by the so-called fast coloration process was proportional to the height of the absorption band at 204 mμ prior to the irradiation. 2. The F-centres formed by the fast process did not contribute to the formation of M-centres. 3. In crystals with a strong absorption band at 204 mμ unstable M-centres were observed, which decayed rapidly after the cessation of the X-irradiation. Their concentration was found to be independent of the F-centre concentration. 4. At temperatures below 0 °C the relation between the concentration of the stable M-centres and the F-centre concentration could not any longer be represented by [M]=k ₁₂·[F₁]·[F₂]+k ₂₂·[F₂]², F₁ and F₂ referring to the F-centres created respectively by the fast and the slow coloration process. Except at very low F₂-centre concentrations however the relationship [M]=k ₀+k ₂·[F₂]² represented the experimental data at all temperatures between ?20 °C and 50 °C. At constant temperaturek ₂ varied withL, the X-ray energy absorbed per unit time and unit volume, according to 1/k ₂=a+bL+cL ². The temperature dependence ofa ^?1 b ^?1 andc ^?1 could be approximated by Boltzmann factors. The corresponding activation energies wereE _a=0.12 eV,E _b=0.53 eV,E _c=0.97 eV.     

Eine empfindliche magnetische Waage zur Bestimmung kleiner Suszeptibilitätsdifferenzen

For a determination of thecarrier susceptibility in a semiconductor sample it is necessary to measure the susceptibilitydifference between different doped samples. The present article describes a susceptibility balance (torsion pendulum) for difference measurements between 140 and 300° K in vacuo. A permanent magnet with cylindrical yoke is used. The achievable accuracy of the susceptibilitydifference amounts to ±0·03% of thewhole susceptibility. The smallest detectable difference in mass susceptibility isΔχ=3 · 10^?11 cgs _m (according to the paramagnetism of 3 · 10¹⁵ electron spins at 140° K).