Surface tension for octafluorocyclobutane, n-butane and their mixtures from 233 K to 254 K, and vapour pressure, excess Gibbs function and excess volume for the mixture at 233 K

1978 ◽  
Vol 2 (3) ◽  
pp. 199-213 ◽  
Author(s):  
Jorge C.G. Calado ◽  
Ian A. McLure ◽  
Virgilio A.M. Soares
1971 ◽  
Vol 24 (4) ◽  
pp. 675 ◽  
Author(s):  
WW Mansfield

The properties of anomalous aqueous condensates, prepared in the manner described by Deryagin,1 vary with aqueous vapour pressure. The changes of column length and of melting point are similar to those of ordinary aqueous solutions. There is no sound evidence that the condensate exhibits abnormal viscosity, density, electrical conductivity, or surface tension.


1986 ◽  
Vol 90 (6) ◽  
pp. 1137-1143 ◽  
Author(s):  
Bernardo Celda ◽  
Agustin Campos ◽  
Juan E. Figueruelo ◽  
Arturo Horta
Keyword(s):  

The behaviour of radon at low temperatures presents some features which have been hitherto difficult to explain. As is well known, this gas can be condensed at the temperature of liquid air, the condensation commencing at about 120° K and being practically complete at 90° K. One would be tempted to conclude that the vapour pressure of radon is extremely small at 90° K. It is clear, however, that in usual conditions radon cannot form a solid phase extending over any area of appreciable size. In fact, the number of atoms in a monatomic layer covering an area of 1 cm 2 is of the order of 10 15 , which corresponds to 57 millicuries of radon, whereas we know that condensation occurs with very much smaller quantities than this. Of course, there is still a possibility that condensed radon exists in the form of microscopic crystals with dimensions, say, of the order of 10 -3 cm. Such crystals would contain some 1013 atoms and would have a well-determined vapour pressure not very different from the vapour pressure of microscopic crystals if the surface tension of radon is not exceptionally large. We see, therefore, that it is possible at least theoretically to treat the problem of condensation of radon from the point of view of a thermodynamical equilibrium between the gaseous and the condensed phase. Very serious objections can, however, be raised against this interpretation. Owing to the investigations of Rutherford, and of Whytlaw-Gray and Ramsay, we know fairly well the vapour pressure of radon in a region of temperatures including the boiling point (210° K) and extending over some 100°. Extrapolating these results to low temperatures, one finds that the vapour pressure of radon at 90° K should be of the order of some tenths of a bar which corresponds to a concentration of some tenths of a millicurie in 1 cm 3 , and is at least 1000 times greater than the amount of gaseous radon in equilibrium with a surface cooled in liquid air. These conclusions are supported by some measurements of the vapour pressure of radon at low temperatures to be described in this paper. In these experiments the volume occupied by radon and the area of the cooled surface were sufficiently small to allow the formation of a polyatomic layer.


2021 ◽  
Author(s):  
Nicole S.M. Vieira ◽  
Margarida L. Ferreira ◽  
Paulo J. Castro ◽  
João M.M. Araújo ◽  
Ana B. Pereiro

This chapter is focused on the massive potential and increasing interest on Fluorinated Ionic Liquids (FILs) as task-specific materials. FILs are a specific family of ionic liquids, with fluorine tags equal or longer than four carbon atoms, that share and improve the properties of both traditional ionic liquids and perfluoro surfactants. These compounds have unique properties such as three nanosegregated domains, a great surfactant power, chemical/biological inertness, easy recovery and recyclability, low surface tension, extreme surface activity, high gas solubility, negligible vapour pressure, null flammability, and high thermal stability. These properties allied to the countless possible combinations between cations and anions allow the design and development of FILs with remarkable properties to be used in specific applications. In this review, we highlight not only the unique thermophysical, surfactant and toxicological properties of these fluorinated compounds, but also their application as task-specific materials in many fields of interest, including biomedical applications, as artificial gas carries and drug delivery systems, as well as solvents for separations in engineering processes.


1944 ◽  
Vol 22a (6) ◽  
pp. 77-94 ◽  
Author(s):  
R. Ruedy

The first and most difficult stage in the condensation of water vapour is the increase in the size of the drops until their radius satisfies the Kelvin–Helmholtz equation for the degree of undercooling or supersaturation reached at the temperature Tc of the vapour; the second stage is the increase in size by continued addition of molecules until the vapour pressure p(v) of the drop containing v molecules approaches the pressure p∞ exerted at the same temperature by a pool of water. A gradual enlargement to visible drops follows. Consideration of the number of collisions of the molecules with the drops forming at the vapour pressure pc of steam, and the loss of molecules by virtue of the higher vapour pressure of small drops leads to the conclusion that at condensation temperatures between 0° and 50 °C. the centres of condensation in the absence of dust or ions contain fewer than a hundred molecules. When the degree of supersaturation corresponds to larger drops, condensation is bound to fail. The conclusion drawn from the theory is confirmed by the values obtained in the tests with flowing steam and with cloud chambers. At higher temperatures larger drops act as nuclei. The growth in the second stage is also extremely rapid, at least until the radius equals in size the wave-length of visible radiation. Water drops of this size, that is, drops that produce coloured diffraction rings, behave as large drops. The heat of condensation may furnish part of the work to be performed against the surface tension.


2013 ◽  
Vol 58 (3) ◽  
pp. 653-659 ◽  
Author(s):  
Antonio Blanco ◽  
Alicia García-Abuín ◽  
Diego Gómez-Díaz ◽  
José M. Navaza ◽  
Óscar L. Villaverde

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