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MAY 16, 1931] NATURE 741

because of the interaction between the electrons, without discontinuity. The jelly has had no way of
there is a finite probability for the energy (and ' knowing ' that the liquid within its meshes has
momentum) of an electron in one part of the core to become a gas. All that remains is to allow the gas
pass directly to another electron in some other part to escape, and there is left behind a coherent aerogel
of the core without the intervening process of radia- of unchanged volume.
tion taking place : that is, in the degenerate core the Silica aerogel with a density so low as 0·1 is very
transfer of energy mostly takes place by the radiation- easy to prepare, and we have prepared some with a
less process and this energy is then converted into density of only 0·02. The silica aerogels are highly
radiation in the non-degenerate envelope surrounding opalescent, although quite transparent ; they display
the core. Because the energy is transferred by the a glassy fracture and small pieces emit a metallic ring
radiationless process, the 'opacity' may be (as in the when dropped.
case of the radioactive atom) considerably higher So far, we have prepared silica, alumina, nickel
than it would be if this transfer of energy took place tartarate, stannic oxide, tungstic oxide, gelatine,
in the form of radiation. We may thus connect the agar, nitrocellulose, cellulose, and egg albumin aerogels
discrepancy in stellar opacity to the same cause as that and see no reason why this list may not be extended
of the internal photoelectric effect in the atom. indefinitely. Apart from the scientific significance
Another interesting point which may be mentioned of these observations, the new physical properties
is that of the emission of high-speed electrons from developed in the materials are of unusual interest.
the white dwarfs, which are almost completely de- S. S. KISTLER.
generate, and hence the chances of collision for an
escaping electron are very small. These high-speed College of the Pacific, Stockton, and
electrons will in some cases have energies comparable Stanford University, California,
to the cosmic radiation. In fact, it can be easily April 8.
seen that due to this electron escape a black dwarf
will lose almost all of its mass-the final state of a
black dwarf is a diffuse mass. These considerations Two Modifications of Liquid Nitrobenzene.
will be published elsewhere in detail. THE changes of dielectric constant and density of
D. S. KoTHARI. liquid nitrobenzene with temperature, studied by one
45 Belvoir Road, Cambridge, of us (J. M.) and described in communications to
April 19. NATURE, suggest that at 9·5° the liquid undergoes an
1
Ellis: a very lucid account is given in Science Progress, April 31,
energy transformation analogous to that found for
p. 615. liquid helium by M. Wolfke and W. H. Keesom, 1 and
' Fowler, Proc. Roy. Soc., vol. 129, p, 1. for liquid ethyl ether by M. Wolfke and J. Mazur. 2
' Milne, Mon. Not. Roy. Ast. Soc., vol. 91, p, 4.
' Obserratory, Feb. 1931, p, 36. To confirm this supposition we have made a study
of the heating curve of carefully chemically purified
nitrobenzene. Nitrobenzene cooled to a temperature
Coherent Expanded Aerogels and Jellies. lower than the point in question (6° C.) was contained
THE continuity of the liquid permeating jellies is in a Dewar vessel provided with a nickel-plated

+_;
demonstrated by diffusion, syneresis, and ultra-
filtration, and the fact that the liquid may be replaced
by other liquids of very diverse character indicates I I ! I
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clearly that the gel structure may be independent of
the liquid in which it is bathed. Hitherto the attempt
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to remove the liquid by evaporation has resulted in
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shrinkage so great that the effect upon the structure


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may be profound. I I i '


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t--_:--t--t-; :
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Mr. Charles Learned and I, with the kindly assistance I i ' i I I i I i


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and advice of Prof. J. W. McBain, undertook to test i ! l
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the hypothesis that the liquid in a jelly can be
replaced by a gas with little or no shrinkage. Our
---+ •
.........!.. --- - ..
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. 'R I i I I I
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efforts have met with complete success. i I I I I
The procedure that we have adopted is as follows :
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The jelly is first formed in a suitable liquid in dilute , '

form. The liquid is then replaced by another which i I I i I I I ! , '


does not dissolve the structure and has a reasonably
I '-/ I ! ! ! '
low critical temperature. Alcohol has proved quite IV ' I I I ! '
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satisfactory for most of the inorganic gels, ether has
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advantages in the case of easily reduced substances, './f I I I j I


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and propane was used for all of the organic jellies.


In making the replacement, it is necessary that each Sec. === )>
liquid used be completely miscible with both that FIG. 1.
which precedes and that which follows it. For
example, water may be replaced by alcohol and then refrigerator. We have studied the change with time
by ether. Mere evaporation would inevitably cause on gradually increasing the temperature of nitro-
shrinkage. However, the jelly is placed in a closed benzene which was isolated from all external dis-
autoclave with an excess of liquid and the temperature turbances.
is raised above the critical temperature of the liquid, The platinum resistance thermometer, calibrated
while the pressure is maintained at all times at or with the aid of the standard thermometer of the
above the vapour pressure, so that no evaporation of Cryogenic Laboratory at Leyden, was used as a stirrer.
liquid can occur and consequently no contraction of The experiments were repeated three times and
the gel can be brought about by capillary forces at they show that at 9·5° there is a distinct slowing down
its surface. of the rate of change of temperature (see the part A B
When the critical temperature is passed, the liquid of the curve, Fig. 1). The parts of the curve above and
has been converted directly into a permanent gas below the point 9·5° are parallel straight lines, which
No. 3211, VoL. 127] u2
© 1931 Nature Publishing Group

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