Ions and Aggregates of Tetra-n-Butylammonium Picrate in Nonaqueous Solvents: A Thermodynamic Study

1971 ◽  
Vol 49 (24) ◽  
pp. 4096-4109 ◽  
Author(s):  
Saul Goldman ◽  
G. C. B. Cave

Values of ΔG0, ΔH0, and ΔS0 at 25 °C were obtained by distribution studies and by calorimetry, for the dimerization and trimerization of tetra-n-butylammonium picrate (1) in anhydrous benzene, chlorobenzene, and o-dichlorobenzene. The standard enthalpy of sublimation of 1 was calculated. The values of ΔG0 for the ionization, dimerization, and trimerization of 1 were linear functions of the reciprocal of the dielectric constant of the solvent. The intercepts and slopes of these graphs are interpreted; partial desolvation of the ions, and of the monomers on association is invoked. A simple potential function is used with the data, in order to deduce suitable models of the dimer and the trimer of 1.

Author(s):  
A. V. Blokhin ◽  
Ya. N. Yurkshtovich

Objectives. Menthol causes a cooling sensation and reduces the nerve activity when it is applied locally, ingested, or inhaled. This feature explains its extensive use as both an aromatizer and a flavoring agent in food manufacturing, tobacco industry, cosmetics production, as well as a mild anesthetic and antiseptic in dentistry. This work aimed to perform a comprehensive thermodynamic study of L-menthol in both crystalline and gaseous states.Methods. To determine the combustion energy of L-menthol in the crystalline state, combustion bomb calorimetry was used. The temperature dependence of L-menthol’s heat capacity in the range of 5–370 K and the melting (fusion) parameters were determined using adiabatic calorimetry. Quantum chemical calculations were performed on a standalone virtual machine in the Google Cloud Platform using an eight-core Intel Xeon Scalable Processor (Skylake) with a 2.0 GHz (up to 2.7 GHz at peak load) clock frequency and 8 GB RAM.Results. The energy and enthalpy of L-menthol combustion in the crystalline state were determined, and the standard enthalpy of L-menthol formation in the gaseous state was calculated using the standard enthalpy of sublimation. The standard thermodynamic functions (reduced enthalpy, entropy, and reduced Gibbs energy) of L-menthol in both crystalline and liquid states were obtained based on the smoothed values of heat capacity and melting parameters. The group of isodesmic reactions for the ab initio calculation of the enthalpy of formation for gaseous L-menthol was substantiated. Electronic energy and frequencies of normal modes of the molecules involved in these reactions were calculated using the Gaussian 4 composite quantum chemical method. Further, the sublimation enthalpy of L-menthol was calculated using the extended Politzer equation according to the electrostatic potential model.Conclusions. The first comprehensive thermodynamic study of L-menthol in various states of aggregation was performed, and the values calculated using semiempirical methods were consistent with the experimental values within error limits, which confirms the reliability of the results.


Geophysics ◽  
1948 ◽  
Vol 13 (4) ◽  
pp. 584-594 ◽  
Author(s):  
Haakon M. Evjen

Based directly on Maxwell’s Field Equations, the extremely low end of the frequency spectrum may be reduced in first approximation to simple potential theory. The approximation theory is borne out by some field experiments, the results of which are presented. Agreement with the theory, however, requires that the ground have a very large effective dielectric constant. This conclusion is supported by previous observations by a number of independent observers. Thus, the relaxation time has been found to be extremely great, not only in observations directly on the ground, but also in small samples of mud, and the sign of an electric anomaly over a relative insulator, such as crystalline salt or gas and oil, invariably has been found to be negative. Both of these observations can be explained in terms of a very great dielectric constant. The value yielded by the present experimental work is of the order of [Formula: see text].


1971 ◽  
Vol 49 (10) ◽  
pp. 1726-1735 ◽  
Author(s):  
Saul Goldman ◽  
G. C. B. Cave

The values of ΔG0 at 25 °C were determined for the ionization, dimerization, and trimerization of tetra-n-butylammonium picrate (1) in benzene, chlorobenzene, and o-dichlorobenzene by a solvent extraction method. Corrections were applied for the presence of hydrates in the organic phase, in order to report ΔG0 values for the anhydrous solvents. In chlorobenzene, hexamers of 1 were also indicated in measurable concentrations. The various values of ΔG0 are related in a simple way to the bulk dielectric constant of the solvent.


2013 ◽  
Vol 32 (6) ◽  
pp. 587-596 ◽  
Author(s):  
Chenhui Liu ◽  
Libo Zhang ◽  
Jinhui Peng ◽  
Wenwen Qu ◽  
Bingguo Liu ◽  
...  

AbstractThe effects of moisture content and temperature on the dielectric property of sodium chloride were investigated by using open-ended senor dielectric measurement system at the frequency of 2.45 GHz. Moisture content is a major influencing factor in the variation of dielectric properties. Dielectric constant, loss factor and loss tangent all increase linearly with moisture content increasing. Three predictive models were developed to obtain dielectric constant, loss factor, loss tangent and of sodium chloride as linear functions of moisture content. Temperature between 20 °C and 100 °C has a positive effect on dielectric constant and loss factor. Penetration depth decreased nonlinearly with moisture and temperature increasing. A predictive model was developed to calculate penetration depth for sodium chloride as a fifth function of moisture content. In addition, the measurements indicate that the particles temperature increases linearly with microwaving heating time at different power levels. The knowledge gained from these results is useful in developing more effective applications of microwave drying and designing better sensors for measuring moisture content of sodium chloride.


2007 ◽  
Vol 452 (1) ◽  
pp. 1-6 ◽  
Author(s):  
R. Pankajavalli ◽  
Ashish Jain ◽  
S. Anthonysamy ◽  
K. Ananthasivan ◽  
P.R. Vasudeva Rao

2005 ◽  
Vol 345 (2-3) ◽  
pp. 96-100 ◽  
Author(s):  
R. Pankajavalli ◽  
K. Ananthasivan ◽  
S. Anthonysamy ◽  
P.R. Vasudeva Rao

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