A metal/liquid interface corrosion-reaction model is developed forthe flow electrification of low-conductivity liquids in metal
pipes. In the proposed model,impurity anions participate in acorrosion reaction at the wall, leaving a net positive ionconcentration in the diffuse electricaldouble layer. Convection of this positive charge constitutes thestreaming current. Theoreticalcalculations for the convected space charge density demonstrate avelocity-dependent entranceeffect that diminishes in
pipes of larger radii, in agreement withexperimental data for heptanein stainless
steel pipes. Far downstream, the proposed model alsocorrectly predicts that theconvected space charge density falls with increasing
pipe radius.As in previous work, theconvected space charge density far downstream,(
I/
Qecb)
, is found tobe
linear with the
-potential. However, the proposed model is self-consistent inthat the
-potential arises aspart of the calculation and is not an adjustable constantcharacteristic only of the metal/hydrocarbon interface. In the entrance region, the convected spacecharge density is assumedto vary exponentially with axial position with the form(
I/
Qecb) =(
I/
Qecb)
-
A(
I/
Qecb)
1×exp(-
), where
A is a preexponentialfactor, (
I/
Qecb)
1 is adeviation function,
is a characteristiceigenvalue, and
is the dimensionless axial coordinate.With a known value of 79.8
m for thesolution Debye length, calculations show
A to be 0.075, and(
I/
Qecb)
1 and
to be7.98 (10
-4),1.42 (10
-4), and 2.60 (10
-5) and 1.242,2.425, and 2.938, respectively, for
pipe radii of 0.24,0.58,and 1.25 mm, respectively.