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Sökning: L773:1063 777X

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1.
  • Aleksandrovskii, A. N., et al. (författare)
  • Low-temperature thermal expansion of pure and inert gas-doped fullerite C60
  • 2003
  • Ingår i: Fizika Nizkikh Temperatur (Kharkov). - : AIP Publishing. - 0132-6414 .- 1816-0328. ; 29:4, s. 432-442
  • Tidskriftsartikel (refereegranskat)abstract
    • The low temperature (2–24 K) thermal expansion of pure (single-crystal and polycrystalline) C60 and polycrystalline C60 intercalated with He, Ne, Ar, and Kr has been investigated using the high-resolution capacitance dilatometer. The investigation of the time dependence of the sample length variations deltaL(t) on heating by deltaT shows that the thermal expansion is determined by the sum of positive and negative contributions, which have different relaxation times. The negative thermal expansion usually prevails at helium temperatures. The positive expansion is connected with the phonon thermalization of the system. The negative expansion is caused by reorientation of the C60 molecules. It is assumed that the reorientation is of a quantum character. The inert gas impurities affect the reorientation of the C60 molecules very strongly, especially at liquid helium temperatures. A temperature hysteresis of the thermal expansion coefficient of Kr– and He–C60 solutions has been revealed. The hysteresis is attributed to orientational polyamorphous transformation in these systems.
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2.
  • Aleksandrovskii, A. N., et al. (författare)
  • Effect of argon on the thermal expansion of fullerite C60 at helium temperatures
  • 2001
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : American Institute of Physics. - 1063-777X .- 1090-6517. ; 27:3, s. 245-246
  • Tidskriftsartikel (refereegranskat)abstract
    • The linear thermal expansion of compacted Ar-doped fullerite C60(ArxC60) is investigated at 2–12 K using a dilatometric method. The thermal expansion of ArxC60 is also studied after partial desaturation of argon from fullerite. It is revealed that argon doping resulted in a considerable change of the temperature dependence of the thermal expansion of fullerite. An explanation of the observed effects is proposed.
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3.
  • Aleksandrovskii, A. N., et al. (författare)
  • Negative thermal expansion of fullerite C60 at helium temperatures
  • 1997
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : AIP Publishing. - 1063-777X .- 1090-6517. ; 23:11, s. 943-946
  • Tidskriftsartikel (refereegranskat)abstract
    • The thermal expansion of fullerite C60 has been measured in the temperature range 2–9 K. A compacted fullerite sample with a diameter of about 6 mm and height of 2.4 mm was used. It was found that at temperatures below ~ 3.4 K the linear thermal expansion coefficient becomes negative. At temperatures above 5 K our results are in good agreement with the available literature data. A qualitative explanation of the results is proposed
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4.
  • Aleksandrovskii, A.N., et al. (författare)
  • On the polyamorphism of fullerite-based orientational glasses.
  • 2005
  • Ingår i: Low Temperature Physics. - : AIP Publishing. - 1063-777X .- 1090-6517. ; 31:5, s. 429-444
  • Tidskriftsartikel (refereegranskat)abstract
    • The dilatometric investigation in the temperature range of 2–28 K shows that a first-orderpolyamorphous transition occurs in the orientational glasses based on C60 doped with H2, D2 andXe. A polyamorphous transition was also detected in C60 doped with Kr and He. It is observed thatthe hysteresis of thermal expansion caused by the polyamorphous transition (and, hence, the transitiontemperature) is essentially dependent on the type of doping gas. Both positive and negativecontributions to the thermal expansion were observed in the low-temperature phase of the glasses.The relaxation time of the negative contribution occurs to be much longer than that of the positivecontribution. The positive contribution is found to be due to phonon and libron modes, whilst thenegative contribution is attributed to tunneling states of the C60 molecules. The characteristictime of the phase transformation from the low-T phase to the high-T phase has been found for theC60–H2 system at 12 K. A theoretical model is proposed to interpret these observed phenomena.The theoretical model proposed, includes a consideration of the nature of polyamorphism inglasses, as well as the thermodynamics and kinetics of the transition. A model of noninteractingtunneling states is used to explain the negative contribution to the thermal expansion. The experimentaldata obtained is considered within the framework of the theoretical model. From the theoreticalmodel the order of magnitude of the polyamorphous transition temperature has been estimated.It is found that the late stage of the polyamorphous transformation is described well by theKolmogorov law with an exponent of n = 1. At this stage of the transformation, the two-dimensionalphase boundary moves along the normal, and the nucleation is not important.
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5.
  • Aleksandrovskii, A.N., et al. (författare)
  • Thermal expansion of fullerite C60 alloyed with argon and neon
  • 2001
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - Woodbury : American Institute of Physics. - 1063-777X .- 1090-6517. ; 27:12, s. 1033-1036
  • Tidskriftsartikel (refereegranskat)abstract
    • The linear thermal expansion of compacted fullerite C60 alloyed with argon (ArxC60) and neon (NexC60) are investigated by a dilatometric method. The experimental temperature is 2–12 K. In the same temperature interval the thermal expansion of ArxC60 and NexC60 are examined after partial desaturation of the gases from fullerite. It is found that Ar and Ne alloying affects the temperature dependence of the thermal expansion coefficient of C60 quite appreciably. The libration and translation contributions to the thermal expansion of pure C60 are separated. The experimental results on the thermal expansion are used to obtain the Debye temperature of pure C60. The effects observed are tentatively interpreted.
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6.
  • Aleksandrovskii, A. N., et al. (författare)
  • Thermal expansion of single-crystal fullerite C60 at helium temperatures
  • 2000
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : AIP Publishing. - 1063-777X .- 1090-6517. ; 26:1, s. 75-80
  • Tidskriftsartikel (refereegranskat)abstract
    • The thermal expansion of single-crystal fullerite C60 has been studied in the range of liquid-helium temperatures (2–10 K). At temperatures below ~4.5 K the thermal expansion of fullerite C60 becomes negative, in agreement with the previous results on polycrystalline materials. A qualitative explanation of the results is proposed.
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7.
  • Alekseeva, L. A., et al. (författare)
  • Determination of the low-temperature self-diffusion coefficient in solid p-H-2 from creep experiments
  • 2018
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : American Institute of Physics (AIP). - 1063-777X .- 1090-6517. ; 44:9, s. 946-951
  • Tidskriftsartikel (refereegranskat)abstract
    • Dependencies of the relative elongation epsilon under the constantly applied stress at T = 1.8 K on the endurance time t of polycrystalline parahydrogen (p-H-2, similar to 0.2% of o-H-2) of high purity (99.9999 mol.%), with varying deuterium content, were measured. The region of linear dependence between the measured creep rates (epsilon) over dot of samples and the applied stress s was revealed. The conclusion that the low-temperature creep of the studied p-H-2 possesses a vacancy-type diffusion character was made on the basis of linear dependence (epsilon) over dot similar to s. Determination of the low-temperature self-diffusion coefficient of vacancies D in solid p-H-2, which characterizes the rate of low-temperature mass transfer, was performed. The cases of migration of vacancies in the crystal bulk, along boundaries separating individual crystallites, as well as between dislocations existing in crystals, are considered. A significant decrease in the (epsilon) over dot and D values with an increase in the isotope concentration in the samples was observed, while maintaining the linear relationship between (epsilon) over dot and s for the studied p-H-2. Published by AIP Publishing.
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8.
  • Alekseeva, L.A., et al. (författare)
  • Unusual changes in the shape of solid parahydrogen with higher than natural isotope content
  • 2016
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : AIP Publishing. - 1063-777X .- 1090-6517. ; 42:6, s. 484-490
  • Tidskriftsartikel (refereegranskat)abstract
    • The relative elongation epsilon of samples of high purity (99.9999 mol. % with respect to nonhydrogenic impurities) parahydrogen (p-H-2, similar to 0.2% o-H-2) with different amounts of the stable hydrogen isotope deuterium is measured as a function of applied stress sigma at temperatures of 1.8-4.2 K. The samples were subjected to uniaxial tension by stepwise loading. The ratio [D]/[H] of the number [D] of deuterium atoms to the number [H] of p-H-2 hydrogen atoms ranged from 0.0055 +/- 0.0005 at. % up to 0.07 at. %. For deuterium enriched p-H-2, the easy slip dislocation stage vanished from the sigma(epsilon) curves and there was a significant reduction in the total relative elongation of the samples, as well as a substantial increase in the hardening coefficient d sigma/d epsilon. Deformation of samples of p-H-2 with deuterium contents higher than the natural amount produces an unusual change in their shape owing to the appearance of a rotational component of the low-temperature plastic mass transfer
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9.
  • Bagatskii, M.I., et al. (författare)
  • Low-temperature dynamics of matrix isolated methane molecules in fullerite C60 : the heat capacity, isotope effects
  • 2014
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : American Institute of Physics (AIP). - 1063-777X .- 1090-6517. ; 40:8, s. 678-684
  • Tidskriftsartikel (refereegranskat)abstract
    • The heat capacity of the interstitial solid solution (CH4)0.4C60 has been investigated in the temperature interval 1.4–120 K. The contribution of CH4 molecules to the heat capacity of the solution has been separated. The contributions of CH4 and CD4 molecules to the heat capacity of the solutions (CH4)0.40C60 and (CD4)0.40C60 have been compared. It is found that above 90 K the character of the rotational motion of CH4 and CD4 molecules changes from libration to hindered rotation. In the interval 14–35 K the heat capacities of CH4 and CD4 molecules are satisfactorily described by contributions of the translational and libration vibrations, as well as the tunnel rotation for the equilibrium distribution of the nuclear spin species. The isotope effect is due to mainly the difference in the frequencies of local translational and libration vibrations of molecules CH4 and CD4. The contribution of the tunnel rotation of the CH4 and CD4 molecules to the heat capacity is dominant below 8 K. The isotopic effect is caused by the difference between both the conversion rates and the rotational spectra of the nuclear spin species of CH4 and CD4 molecules. The conversion rate of CH4 molecules is several times lower than that of CD4 ones. Weak features observed in the curves of temperature dependencies of the heat capacity of CH4 and CD4 molecules near 6 and 8 K, respectively, are most likely a manifestation of first-order polyamorphic phase transitions in the orientational glasses of these solutions.
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10.
  • Bagatskii, M. I., et al. (författare)
  • Low-temperature heat capacity of fullerite C-60 doped with deuteromethane
  • 2012
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - Melville, NY : American Institute of Physics (AIP). - 1063-777X .- 1090-6517. ; 38:1, s. 67-73
  • Tidskriftsartikel (refereegranskat)abstract
    • The heat capacity C of fullerite doped with deuteromethane (CD4)(0.4)(C-60) has been investigated in the temperature interval 1.2-120K. The contribution Delta C-CD4 of the CD4 molecules to the heat capacity C has been isolated. It is shown that at T approximate to 120K the rotational motion of CD4 molecules in the octahedral voids of the C-60 lattice is weakly hindered. When the temperature is lowered to 80K, the rotational motion of the CD4 molecules changes from weakly hindered rotation to libration. In the range T = 1.2-30 K, Delta C-CD4 is described quite accurately by the sum of contributions from the translational and librational vibrations and tunneling rotation of CD4 molecules. The contribution of tunneling rotation to the heat capacity Delta C-CD4(T) is dominant below 5K. The effect of nuclear-spin conversion of the CD4 molecules on the heat capacity has been observed and the characteristic times for nuclear spin conversion between the lowest levels of the A- and T-species of CD4 molecules at T < 5K have been estimated. A feature observed in Delta C-CD4(T) near T = 5.5K is most likely a manifestation of a first-order phase transition in the orientational glass form of the solution. (C) 2012 American Institute of Physics. [doi: 10.1063/1.3677237]
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