S C Mehrotra
Articles written in Pramana – Journal of Physics
Volume 13 Issue 4 October 1979 pp 447-449 Spectrescopy
Microwave spectral line widths of the transition
Volume 20 Issue 6 June 1983 pp 439-449 Atomic And Molecular Physics
The longitudinal relaxation time
Volume 21 Issue 1 July 1983 pp 35-39 Molecular Physics
The theoretical calculation of line widths and line shifts for CO2-Ar system is computed by the Mehrotra-Boggs theory. It is shown for this system that the phase shift effect is very important at large values of |
Volume 35 Issue 1 July 1990 pp 81-87
When the collisional dynamics of two states under consideration for a radiative transition is different, the polarization and population relaxations in gas phase at low pressure are governed by four-, instead of three-, coupled Bloch-type equations. The general transient solutions of these four-coupled equations are solved by using the Laplace transformation technique. It has been found that an additional exponential term appears because of the effect. This is also responsible for the non-exponential character in the decay signal of a transient microwave pulse experiment, besides other factors reported earlier.
Volume 44 Issue 1 January 1995 pp 33-44
The dielectric relaxation studies of 4-ethylphenol-methanol mixtures have been carried out at various temperatures ranging from 10°C to 40°C using time domain reflectometry in the frequency range 10 MHz to 10 GHz. The relaxation mechanism in these systems is explained by Cole-Davidson model. The excess dielectric parameters, Kirkwood correlation factor and activation energy have been calculated and discussed with respect to molecular arrangements, and microdynamics of the binary mixture composed of both the associative type of liquids.
Volume 44 Issue 5 May 1995 pp 405-410
Time domain reflectometry method has been used in the frequency range of 10 MHz to 10 GHz to determine dielectric properties of aqueous solutions of acetonitrile in temperature range of 0°C to 40°C. The calibration method based on the least squares fit method has been used. The excess permittivity, activation energy, Kirkwood correlation factor and activation energy of acetonitrile-water system have also been determined. The dielectric data show that acetonitrile molecules interact such that the dipoles have a tendency to remain antiparallel.
Volume 45 Issue 1 July 1995 pp 19-24
Dielectric properties of nitriles have been studied using time domain reflectometry in the frequency range of 10 MHz to 10 GHz over the temperature range of 0°C to 45°C. The calculated dielectric relaxation parameters are compared with values for the corresponding n-alcohols. The dielectric behaviour in n-nitrile systems is quite different from the corresponding behaviour in n-alcohols. The dipoles in n-nitrile systems show a tendency to remain antiparallel, unlike in alcohol systems. The activation energy decreases with the increase of molecular size, whereas in hydrogen bonded liquid it increases.
Volume 46 Issue 2 February 1996 pp 91-98
The complex permittivity, static dielectric constant and relaxation time for tetrahydrofuran-water and acetone-water mixtures have been determined at 0°, 10°, 25° and 35°C using time domain reflectometry technique (TDR). The behaviour of relaxation time of the mixture shows a maxima for the mixture with 30% of water by volume. This suggests that the tendency to form cluster between water and solute molecule is maximum for this mixture. The excess permittivity for both tetrahydrofuran-water mixture and acetone-water mixtures, are found to be negative. The Kirkwood correlation factor has been determined at various concentrations of water. Static dielectric constant for the mixtures have been fitted well with the modified Bruggeman model. The values of the Bruggeman parameter
Volume 59 Issue 4 October 2002 pp 693-699 Brief Reports
The dielectric relaxation parameters, viz., static dielectric constant,
Volume 93 | Issue 5
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