Ürst sheet in the solution. In the
Helmholtz model the double layer is
regarded as consisting of two planes
of charge, with the inner plane of
ions from the solution being caused
by the charge on the electrode and
the outer plane being caused by op-
positely charged ions in the solution
responding to theÜrst layer of ions.
In the *Gouy–Chapman model (dif-
fuse double layer) thermal motion of
ions is taken into account. Neither
model is completely successful since
the Helmholtz model exaggerates the
rigidity of the structure of the
charges and the Gouy–Chapman
model underestimates the rigidity of
the structure. The Stern model im-
proves on both models by assuming
that the ions next to the electrode
have a rigid structure, while taking
the second layer to be as described
by the Gouy–Chapman model.
electric-arc furnace A furnace
used in melting metals to make al-
loys, especially in steel manufacture,
in which the heat source is an elec-
tric arc. In the direct-arc furnace,
such as the Héroult furnace, an arc is
formed between the metal and an
electrode. In the indirect-arc furnace,
such as the Stassano furnace, the arc
is formed between two electrodes
and the heat is radiated onto the
metal.
electrochemical cell See cell.
electrochemical equivalent
Symbol z. The mass of a given el-
ement liberated from a solution of its
ions in electrolysis by one coulomb
of charge. See faraday’s laws.
electrochemical series See elec-
tromotive series.
electrochemistry The study of
chemical properties and reactions in-
volving ions in solution, including
electrolysis and electric cells.
electrochromatography See elec-
trophoresis.
electrocyclic reaction A type of
cyclic rearrangement in which a
sigma bond is formed between two
terminal carbon atoms of a conju-
gated molecule, resulting in a de-
crease of one in the number of pi
bonds present.
electric-arc furnace 194
e
Electrocyclic reaction
electrode 1.A conductor that
emits or collects electrons in a cell,
thermionic valve, semiconductor de-
vice, etc. The anodeis the positive
electrode and the cathodeis the neg-
ative electrode. 2.See half cell.
electrodeposition The process of
depositing one metal on another by
electrolysis, as in *electroforming
and *electroplating.
electrode potential The potential
difference produced between the
electrode and the solution in a *half
cell. It is not possible to measure this
directly since any measurement in-
volves completing the circuit with
the electrolyte, thereby introducing
another half cell. Standard electrode
potentialsEŠare deÜned by measur-
ing the potential relative to a stan-
dard *hydrogen half cell using 1.0
molar solution at 25°C. The conven-
tion is to designate the cell so that
the oxidized form is writtenÜrst. For
example,
Pt(s)|H 2 (g)H+(aq)|Zn2+(aq)|Zn(s)
The e.m.f. of this cell is –0.76 volt (i.e.
the zinc electrode is negative). Thus
the standard electrode potential of
the Zn2+|Zn half cell is –0.76 V. Elec-
trode potentials are also called reduc-