Temperature Dependence of the Permittivity of o-Nitroanisole-Benzene and o-Nitroanisole-Carbon Tetrachloride Mixtures in the Vicinity of its Melting Point

1993 ◽  
Vol 97 (5) ◽  
pp. 731-736 ◽  
Author(s):  
B. Szurkowski ◽  
T. Hilczer ◽  
M. Saliwińska-Bartkowiak
Keyword(s):  
Melting Point ◽  
Carbon Tetrachloride ◽  
Temperature Dependence

Conductivity and Viscosity of the Tetrabutylammonium Bromide – Carbon Tetrachloride System

1972 ◽  
Vol 50 (10) ◽  
pp. 1600-1603 ◽  
Author(s):  
K. F. Denning ◽  
James A. Plambeck
Keyword(s):  
Carbon Tetrachloride ◽  
Temperature Dependence ◽  
Tetrabutylammonium Bromide ◽  
Viscosity Measurements ◽  
Ratio Range

Conductivity and viscosity measurements have been made on tetra-n-butylammonium bromide – carbon tetrachloride solutions for the mole ratio range 1:40 to 1:2 at temperatures from 25 to 40 °C. At any individual concentration, both conductivity and viscosity follow an Arrhenius type temperature dependence. Viscosity increases exponentially with tetrabutylammonium bromide concentration while conductivity has a maximum at approximately 1:5 mole ratio R4NBr–CCl4.

scholarly journals Thermochromism of Highly Luminescent Photopolymer Flexible Films Based On Eu (III) Salts Confined in Polysulfone

Materials ◽  
2020 ◽  
Vol 13 (23) ◽  
pp. 5394
Author(s):  
Mani Outis ◽  
João Paulo Leal ◽  
Maria Helena Casimiro ◽  
Bernardo Monteiro ◽  
Cláudia Cristina Lage Pereira
Keyword(s):  
Thermal Stability ◽  
Ionic Liquid ◽  
Melting Point ◽  
Quantum Yield ◽  
Thermal Behavior ◽  
Temperature Dependence ◽  
Strong Temperature Dependence ◽  
Host Matrix ◽  
Flexible Films ◽  
First Time

Here we discuss the influence of two different cations on the emissive properties of the highly emissive [Eu(fod)4]− anion. The studied Eu(III) salts were [C16Pyr][Eu(fod)4] (1), and the previously reported [Chol][Eu(fod)4]. C16Pyr stands for N-cetylpyridinium, Chol for cholinium and fod for 1,1,1,2,2,3,3-heptafluoro-7,7-dimethyloctane-4,6-dionate. 1 is classified as ionic liquid, with melting point close to 60 °C, and presented a luminescence quantum yield of (ϕ) 100%. Ultrabright emissive photopolymers were obtained for the first time using polysulfone as the host matrix. The films were prepared with incorporation of 10% (w/w) of 1 and [Chol][Eu(fod)4] in the polymeric matrix, which improved its thermal stability. Additionally, the luminescence of CholEu(fod)4/PSU presented a strong temperature dependence with a ratiometric thermal behavior.

scholarly journals Effects of Local Heating and Premelting in the Terminal Part of the e+ Track

2012 ◽  
Vol 733 ◽  
pp. 15-18 ◽  
Author(s):  
Dmitry Zvezhinskiy ◽  
Sergey V. Stepanov ◽  
Vsevolod Byakov ◽  
Bożena Zgardzińska
Keyword(s):  
Melting Point ◽  
Temperature Dependence ◽  
Local Heating ◽  
Bulk Temperature ◽  
Melting Points ◽  
Terminal Part ◽  
Slowing Down ◽  
Positronium Lifetime ◽  
Molten Region

The terminal part of the e+ track (the positron blob) is formed during ionization slowing down and subsequent ion-electron recombinations produced by a positron. It releases up to 1 keV of energy, which is converted into heat within few picoseconds. If a bulk temperature of a medium is below, but close enough to its melting point, some region of a substance may melt, yielding a peculiar temperature dependence of the lifetime (LT) spectra. We have estimated properties of the molten region with a help of macroscopic heat con- duction equation and suggested a model describing temperature dependence of the ortho- positronium lifetime in frozen methanol, ethanol, butanol and water close to their melting points.

Temperature dependence of proton magnetic resonance solvent shifts. 3,5-Dichlorosalicylaldehyde in carbon tetrachloride and benzene

1968 ◽  
Vol 46 (19) ◽  
pp. 3110-3112 ◽  
Author(s):  
G. Kotowycz ◽  
T. Schaefer
Keyword(s):  
Carbon Tetrachloride ◽  
Temperature Dependence ◽  
Proton Magnetic Resonance ◽  
Benzene Solution ◽  
Chemical Shifts ◽  
Relative Temperature ◽  
Proton Shift ◽  
Solvent Shifts ◽  
Solvent Molecules ◽  
Proton Chemical Shifts

The ring proton chemical shifts of 3,5-dichlorosalicylaldehyde as a function of temperature in carbon tetrachloride and benzene solutions indicate that if there is association with solvent molecules in benzene solution, then there is also association with carbon tetrachloride solvent molecules. The aldehydic proton shift shows a much smaller (relative) temperature dependence in the carbon tetrachloride solution.

EFFECT OF IMPURITIES ON THE DIELECTRIC PROPERTIES OF OLEIC ACID

2012 ◽  
Vol 02 (03) ◽  
pp. 1250014
Author(s):  
F. F. DE SOUSA ◽  
P. T. C. FREIRE ◽  
J. MENDES FILHO ◽  
A. C. OLIVEIRA ◽  
E. LONGHINOTTI ◽  
...  
Keyword(s):  
Dielectric Constant ◽  
Dipole Moment ◽  
Oleic Acid ◽  
Dielectric Properties ◽  
Melting Point ◽  
Temperature Dependence ◽  
Effect Of Impurities ◽  
Correlation Parameters

Temperature dependence of the dielectric constant of oleic acid with different degrees of purity was measured in the 233–313 K range. It was observed that the presence of impurities (palmitic and linolenic acids) strongly influences the dielectric constant, melting point and dipole moment of the oleic acid. The values of apparent dipole moment and the Kirkwood correlation parameters were evaluated using the Kirkwood's model and were estimated to be about 1.20, 1.61 and 2.27 D, respectively for 60, 90 and 97 wt% oleic acid.

Temperature dependence of chemical shifts of protons in hydrogen bonds. Experimental evidence on an intramolecular hydrogen bond

1968 ◽  
Vol 46 (17) ◽  
pp. 2865-2868 ◽  
Author(s):  
T. Schaefer ◽  
G. Kotowycz
Keyword(s):  
Hydrogen Bond ◽  
Carbon Tetrachloride ◽  
Chemical Shift ◽  
Hydrogen Bonds ◽  
Temperature Dependence ◽  
Intramolecular Hydrogen Bond ◽  
Chemical Shifts ◽  
Hydroxyl Proton ◽  
Intramolecular Hydrogen ◽  
Strong Intramolecular Hydrogen Bond

A temperature dependence of the chemical shift of the hydroxyl proton in the strong intramolecular hydrogen bond in 3,5-dichlorosalicylaldehyde is observed in carbon tetrachloride and benzene-d6 solutions. Its magnitude of 0.25 to 0.30 × 10−2 p.p.m. per ° C over a range of 100 °C is in agreement with the model described by Muller and Reiter (1).

scholarly journals On the Temperature Dependence of Vaporization Enthalpy and its Correlation with Surface Tension.

2021 ◽  
Author(s):  
Amin Alibakhshi ◽  
Bernd Hartke
Keyword(s):  
Surface Tension ◽  
Critical Temperature ◽  
Melting Point ◽  
Temperature Dependence ◽  
Wide Temperature Range ◽  
Thermophysical Properties ◽  
Vaporization Enthalpy ◽  
Temperature Range

Temperature dependence of vaporization enthalpy is one of the most important thermophysical properties of compounds. In the present study, we theoretically developed relationships applicable to evaluation of vaporization enthalpy of compounds from diverse chemical families for a wide temperature range from melting point to the critical temperature. One outcome of the proposed approach is a relationship describing the correlation between the surface tension and vaporization enthalpy which outperforms the extensively applied Kabo method proposed for the same purpose.<br>

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