The Romance of Modern Chemistry
Forfatter: James C. Phillip
År: 1912
Forlag: Seeley, Service & Co. Limited
Sted: London
Sider: 347
UDK: 540 Phi
A Description in non-technical Language of the diverse and wonderful ways in which chemical forces are at work and of their manifold application in modern life.
With 29 illustrations & 15 diagrams.
Søgning i bogen
Den bedste måde at søge i bogen er ved at downloade PDF'en og søge i den.
Derved får du fremhævet ordene visuelt direkte på billedet af siden.
Digitaliseret bog
Bogens tekst er maskinlæst, så der kan være en del fejl og mangler.
CHEMISTRY AND ELECTRICITY
the fused salt itself, decomposition took place, with the
result that the metallic part of the salt was liberated at
one wire (the cathode), and the acidic part of the salt at
the other wire (the anode). Investigation, indeed, has
shown that the passage of an electric current through
a salt solution consists in a general movement of the
metallic part towards the cathode, and a general move-
ment of the acidic part in the opposite direction; but
most obvious to the onlooker is what happens at the
wires or electrodes.
What the observer sees taking place at the electrodes is
sometimes only the secondary, not the direct, result of
electrolysis. I1 or instance, if we were to pass a current
through a solution of common salt, or sodium chloride,
to give it the systematical chemical name, the metallic
part of the salt, the sodium, would be liberated primarily
at the cathode. Any particle of sodium, however, which
was thus liberated, would immediately be set upon by
the surrounding water molecules; hydrogen gas would be
evolved, and caustic soda would be formed in solution
round the cathode. The action of water on sodium
prevents our obtaining this metal by the electrolysis of an
aqueous solution of any sodium salt.
Sometimes the wire or plate which forms the anode is
attacked and dissolved by the acidic part of the salt which
is being electrolysed. An interesting example of this
is furnished by the electrolysis of a solution of copper
sulphate between copper electrodes. During this process
the metallic part of the salt, the copper, is deposited on
the cathode, which therefore becomes gradually heavier.
The sulphate, or acidic part of the salt, instead of being
liberated at the copper anode, attacks it, forming copper
sulphate, which dissolves in the water. So the net
298