On orientational relief of inter-molecular potential and the structure of domain walls in fullerite C60

A simple planar model for an orientational ordering of threefold molecules on a triangular lattice modelling a close-packed (111) plane of fullerite is considered. The system has 3-sublattice ordered ground state which includes 3 different molecular orientations. There exist 6 kinds of orientational domains, which are related with a permutation or a mirror symmetry. Interdomain walls are found to be rather narrow. The model molecules have two-well orientational potential profiles, which are slightly effected by a presence of a straight domain wall. The reason is a stronger correlation between neighbour molecules in triangular lattice versus previously considered square lattice A considerable reduction (up to one order) of orientational interwell potential barrier is found in the core regions of essentially two-dimentional potential defects, such as a three-domain boundary or a kink in the domain wall. For ultimately uncorrelated nearest neighbours the height of the interwell barrier can be reduced even by a factor of 100.Comment: 11 pages, 13 figures, LaTeX, to appear in Low Temperature Physic

Flow analysis of viscoelastic liquid film in a rotational mixer

The flow of a viscoelastic liquid film in a field of centrifugal forces was studied within the framework of the Oldroyd model. © 1978 Plenum Publishing Corporation

Evolution of forest pedogenesis in the south of the forest-steppe of the Central Russian Upland in the Late Holocene

The Late Holocene stage of forest pedogenesis has been studied on the interfluves along river valleys in the forest-steppe zone of the Central Russian Upland. The development of gray forest soils from the former chernozems as a result of the Late Holocene advance of forest vegetation over steppes is discusse

Low temperature thermal expansion of pure and inert gas-doped Fullerite C60

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 high-resolution capacitance dilatometer. The investigation of the time dependence of the sample length variations on heating 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 quantum character. The inert gas impurities affect very strongly the reorientation of the C60 molecules 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.Comment: 18 pages, 12 figure

Thermal expansion of solid solutions Kr-CH4 at temperatures of liquid helium

A negative contribution of the CH4 impurity to the thermal expansion of the solution has been revealed in dilatometric studies of solid Kr+0.76% CH4, Kr+5.25% CH4 and Kr+10.5% CH4 solutions at 1-23 K. It is shown that the negative contribution results from changes in the occupancy of the ground state of the A-modifications of isolated CH4 molecules. Assuming that the CH4 impurity singles and clusters contribute to the thermal expansion independently, we can estimate their contributions. The contribution of the singles to the thermal expansion of the solid solution is negative. The energies of the first excitational rotational states were determined for singles and two-body and three-body clusters of CH4 molecules.Comment: 10 pages, 7 figure

Thermal expansion of solid solutions Kr-CH₄ at temperatures of liquid helium

A negative contribution of the CH₄ impurity to the thermal expansion of the solution has been revealed in the dilatometric studies of solid Kr + 0.76% CH4, Kr + 5.25% CH₄, and Kr + 10.5% CH₄ solutions at 1-23 K. It is shown that the negative contribution results from changes in the occupancy of the ground state of the A-modifications of isolated CH₄ molecules. Assuming that the CH₄ impurity singles and clusters contribute to the thermal expansion independently, we can estimate their contributions. The contribution of the singles to the thermal expansion of the solid solution is negative. The energies of the first excitational rotational states were determined for singles and two-body and three-body clusters of the CH₄ molecules

On the polyamorphism of fullerite-based orientational glasses

The dilatometric investigation in the temperature range of 2-28K shows that a first-order polyamorphous transition occurs in the orientational glasses based on C60 doped with H2, D2 and Xe. A polyamorphous transition was also detected in C60 doped with Kr and He. It is observed that the hysteresis of thermal expansion caused by the polyamorphous transition (and, hence, the transition temperature) is essentially dependent on the type of doping gas. Both positive and negative contributions 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 positive contribution. The positive contribution is found to be due to phonon and libron modes, whilst the negative contribution is attributed to tunneling states of the C60 molecules. The characteristic time of the phase transformation from the low-T phase to the high-T phase has been found for the C60-H2 system at 12K. A theoretical model is proposed to interpret these observed phenomena. The theoretical model proposed, includes a consideration of the nature of polyamorphism in glasses, as well as the thermodynamics and kinetics of the transition. A model of non-interacting tunneling states is used to explain the negative contribution to the thermal expansion. The experimental data obtained is considered within the framework of the theoretical model. From the theoretical model 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 the Kolmogorov law with an exponent of n=1. At this stage of the transformation, the two-dimensional phase boundary moves along the normal, and the nucleation is not important.Comment: 29 pages, 14 figures, added references, corrected typo

Low temperature thermal expansion of fullerite C₆₀ alloyed with argon and neon

Динамика кристаллической решетки 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

Argon effect on thermal expansion of fullerite C₆₀

The linear thermal expansion of compacted Ar-doped fullerite C₆₀(ArxC₆₀) is investigated at 2-12 K using dilatometric method. The thermal expansion of ArxC₆₀ was also studied after partial desaturation of argon from fullerite. It is revealed that argon doping resulted in the considerable change of the temperature dependence of the thermal expansion of fullerite. An explanation of the observed effects is proposed

Mapping of periodically poled crystals via spontaneous parametric down-conversion

A new method for characterization of periodically poled crystals is developed based on spontaneous parametric down-conversion. The method is demonstrated on crystals of Y:LiNbO3, Mg:Y:LiNbO3 with non-uniform periodically poled structures, obtained directly under Czochralski growth procedure and designed for application of OPO in the mid infrared range. Infrared dispersion of refractive index, effective working periods and wavelengths of OPO were determined by special treatment of frequency-angular spectra of spontaneous parametric down-conversion in the visible range. Two-dimensional mapping via spontaneous parametric down-conversion is proposed for characterizing spatial distribution of bulk quasi-phase matching efficiency across the input window of a periodically poled sample.Comment: 19 pages, 6 figure