Isothermal Vapor Pressures of Three Binary Systems: n-Tetradecane + Methyl Dodecanoate, Methyl Tetradecanoate, or Methyl Hexadecanoate between 353.15 and 453.15 K

2017 ◽  
Vol 62 (6) ◽  
pp. 1842-1852
Author(s):  
Lakhdar Sahraoui ◽  
Kamel Khimeche ◽  
Ilham Mokbel ◽  
Mokhtar Benziane ◽  
Jacques Jose
1990 ◽  
Vol 16 (6) ◽  
pp. 1263-1265 ◽  
Author(s):  
Masaru Hongo ◽  
Mitsuhisa Kusunoki ◽  
Kenji Mishima ◽  
Yasuhiko Arai

1970 ◽  
Vol 48 (20) ◽  
pp. 3173-3184 ◽  
Author(s):  
A. N. Campbell ◽  
G. M. Musbally

The saturation vapor pressures of ten mixtures of the binary systems (1) acetone – chloroform, (2) acetone – carbon tetrachloride, and (3) benzene – carbon tetrachloride have been determined, from 100 to 230° for system 1 and from 100° up to the highest temperature at which liquid and vapor coexist for systems 2 and 3. The system acetone – chloroform could not be studied at higher temperatures because of decomposition.The gas–liquid critical temperatures of the three binary systems have been determined by the disappearance of meniscus method. The orthobaric compositions of the vapour–liquid equilibria of the binary systems have been measured from 100 to 180° for system 1 and from 100° to the critical region for systems 2 and 3, using a glass bomb enclosed in a steel bomb.From the vapour–liquid composition curves and the vapor pressure curves at constant temperatures (100, 150, 160, 170, and 180°), the existence of an azeotrope in the system acetone–chloroform at these temperatures, and having a composition of 36.2 mole% acetone at 100°, was confirmed. The composition of the azeotrope shifts towards lower acetone content as the temperature is raised. Azeotropes were not found in the systems acetone – carbon tetrachloride and benzene – carbon tetrachloride, over the ranges of temperature and pressure of this research.The data of the binary systems were treated thermodynamically to yield the liquid phase activity coefficients and, as suggested by Chueh and Prausnitz, the Redlick–Kwong equation was used in a modified form to obtain the fugacity coefficients of components in the vapor phase. Several liquid phase parameters, such as the binary interaction constant, Henry's constant, and dilation constant have been calculated, using the van Laar equation as modified by Chueh and Prausnitz.


1966 ◽  
Vol 44 (10) ◽  
pp. 1183-1189 ◽  
Author(s):  
A. N. Campbell ◽  
E. M. Kartzmark ◽  
R. M. Chatterjee

The volume changes on mixing of the three binary mixtures, acetone–chloroform, benzene–chloroform, acetone–benzene, and the ternary mixture, acetone–chloroform–benzene, and their molar refractivities and viscosities, were determined.Determinations of total and partial vapor pressures were made. The systems acetone–chloroform and benzene–chloroform show negative deviations from Raoult's law. The system acetone–benzene shows positive deviations.The excess Gibbs free energies of mixing have been calculated for all systems. By combining these data with previously measured heats of mixing (1), the excess entropy has also been calculated. The curves representing zero excess volume, zero heat of mixing, zero excess free energy of mixing, and zero excess viscosity as functions of composition in the ternary system do not coincide. It, therefore, must be concluded that they result from compensating effects and do not represent ideality.


1965 ◽  
Vol 5 ◽  
pp. 120-130
Author(s):  
T. S. Galkina

It is necessary to have quantitative estimates of the intensity of lines (both absorption and emission) to obtain the physical parameters of the atmosphere of components.Some years ago at the Crimean observatory we began the spectroscopic investigation of close binary systems of the early spectral type with components WR, Of, O, B to try and obtain more quantitative information from the study of the spectra of the components.


1979 ◽  
Vol 46 ◽  
pp. 77-88
Author(s):  
Edward L. Robinson

Three distinct kinds of rapid variations have been detected in the light curves of dwarf novae: rapid flickering, short period coherent oscillations, and quasi-periodic oscillations. The rapid flickering is seen in the light curves of most, if not all, dwarf novae, and is especially apparent during minimum light between eruptions. The flickering has a typical time scale of a few minutes or less and a typical amplitude of about .1 mag. The flickering is completely random and unpredictable; the power spectrum of flickering shows only a slow decrease from low to high frequencies. The observations of U Gem by Warner and Nather (1971) showed conclusively that most of the flickering is produced by variations in the luminosity of the bright spot near the outer edge of the accretion disk around the white dwarf in these close binary systems.


Author(s):  
John T. Armstrong

One of the most cited papers in the geological sciences has been that of Albee and Bence on the use of empirical " α -factors" to correct quantitative electron microprobe data. During the past 25 years this method has remained the most commonly used correction for geological samples, despite the facts that few investigators have actually determined empirical α-factors, but instead employ tables of calculated α-factors using one of the conventional "ZAF" correction programs; a number of investigators have shown that the assumption that an α-factor is constant in binary systems where there are large matrix corrections is incorrect (e.g, 2-3); and the procedure’s desirability in terms of program size and computational speed is much less important today because of developments in computing capabilities. The question thus exists whether it is time to honorably retire the Bence-Albee procedure and turn to more modern, robust correction methods. This paper proposes that, although it is perhaps time to retire the original Bence-Albee procedure, it should be replaced by a similar method based on compositiondependent polynomial α-factor expressions.


Author(s):  
Douglas L. Dorset

A variety of linear chain materials exist as polydisperse systems which are difficultly purified. The stability of continuous binary solid solutions assume that the Gibbs free energy of the solution is lower than that of either crystal component, a condition which includes such factors as relative molecular sizes and shapes and perhaps the symmetry of the pure component crystal structures.Although extensive studies of n-alkane miscibility have been carried out via powder X-ray diffraction of bulk samples we have begun to examine binary systems as single crystals, taking advantage of the well-known enhanced scattering cross section of matter for electrons and also the favorable projection of a paraffin crystal structure posited by epitaxial crystallization of such samples on organic substrates such as benzoic acid.


Author(s):  
M. Yamada ◽  
K. Ueda ◽  
K. Kuboki ◽  
H. Matsushima ◽  
S. Joens

Use of variable Pressure SEMs is spreading among electron microscopists The variable Pressure SEM does not necessarily require specimen Preparation such as fixation, dehydration, coating, etc which have been required for conventional scanning electron microscopy. The variable Pressure SEM allows operating Pressure of 1˜270 Pa in specimen chamber It does not allow microscopy of water-containing specimens under a saturated vapor Pressure of water. Therefore, it may cause shrink or deformation of water-containing soft specimens such as plant cells due to evaporation of water. A solution to this Problem is to lower the specimen temperature and maintain saturated vapor Pressures of water at low as shown in Fig. 1 On this technique, there is a Published report of experiment to have sufficient signal to noise ratio for scondary electron imaging at a relatively long working distance using an environmental SEM. We report here a new low temperature microscopy of soft Plant cells using a variable Pressure SEM (Hitachi S-225ON).


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