NOTE ON THE DIELECTRIC CONSTANTS OF ETHYL CHLORIDE AND n-BUTANE ADSORBED ON NONPOROUS TiO2

1953 ◽  
Vol 31 (11) ◽  
pp. 998-1003 ◽  
Author(s):  
M. H. Waldman ◽  
J. A. Snelgrove ◽  
R. Mcintosh

The dielectric constants of ethyl chloride and n-butane adsorbed on nonporous TiO2 were measured. The plot of capacity change versus volume adsorbed was found to reveal two linear sections in the case of ethyl chloride with an abrupt change in the slope of the plot occurring at the Vm value calculated using the B.E.T. or Hüttig adsorption equations. With n-butane the plot was linear beyond Vm. For ethyl chloride on rutile a slight temperature dependence in the polarization was observed for the volume of gas adsorbed above Vm, while a negligible temperature dependence was noted for the portion below Vm. It is postulated that the observations with the polar gas on the nonporous rutile can be explained by a change from oscillatory to rotational motion of the adsorbed molecule after the monolayer is complete. It was noted that gases adsorbed on nonporous TiO2 behaved differently from gases adsorbed on porous silica gel. This appears to lead to the necessity of postulating changes of density for the adsorbed phase on silica gel.

1947 ◽  
Vol 25b (6) ◽  
pp. 566-574 ◽  
Author(s):  
R. McIntosh ◽  
L. McLeod ◽  
H. S. Johnson ◽  
N. Hollies

A measure of the dielectric constants of several substances adsorbed on silica gel has been obtained by measuring the change in the capacity of an electrical condenser when measured amounts of the substances were adsorbed on silica gel situated between the plates of the condenser. The substances examined were ethyl chloride, n-butane, and ethylene oxide. The plot of capacity change vs. amount adsorbed was found, in all cases, to consist of two or more quite distinct sections, each approximating to linearity. The temperature coefficients of dielectric constant were evaluated. The dielectric constant calculated for adsorbed n-butane was close to that calculated for the bulk liquid, whereas the value calculated for adsorbed ethyl chloride was significantly lower than the value calculated for the liquid.


1995 ◽  
Vol 190 (3) ◽  
pp. 206-211 ◽  
Author(s):  
S. Satoh ◽  
I. Matsuyama ◽  
K. Susa

2008 ◽  
Vol 18 (24) ◽  
pp. 2833 ◽  
Author(s):  
Joanna Claire Rooke ◽  
Alexandre Léonard ◽  
Hugo Sarmento ◽  
Jean-Pierre Descy ◽  
Bao-Lian Su

1978 ◽  
Vol 173 (1) ◽  
pp. 245-254 ◽  
Author(s):  
T Feizi ◽  
R A Childs ◽  
S I Hakomori ◽  
M E Powell

More than ten new types of gangliosides, in addition to haematoside and sialosylparagloboside, were isolated from human erythrocyte membranes. These were separated by successive chromatographies on DEAE-Sephadex, on porous silica-gel columns and on thin-layer silica gel as acetylated compounds. Highly potent blood-group-Ii and moderate blood-group-H activities were demonstrated in some of the ganglioside fractions. The gangliosides incorporated into cholesterol/phosphatidylcholine liposomes stoicheiometrically inhibited binding of anti-(blood-group I and i) antibodies to a radioiodinated blood-group-Ii-active glycoprotein. The fraction with the highest blood-group-I-activity, I(g) fraction, behaved like sialosyl-deca- to -dodeca-glycosylceramides on t.l.c. Certain blood-group-I and most of the -i determinants were in partially or completely cryptic form and could be unmasked by sialidase treatment. Thus the I and i antigens, which are known to occur on internal structures of blood-group-ABH-active glycoproteins in secretions, also occur in the interior of the carbohydrate chains of erythrocyte gangliosides.


1987 ◽  
Vol 26 (S3-1) ◽  
pp. 275 ◽  
Author(s):  
K. I. Blum ◽  
S. Murphy ◽  
M. H. W. Chan ◽  
D. D. Awschalom ◽  
J. D. Reppy

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