hours, 4 hours and 6 hours. The lower part, respectively presented the surface morphologies of test
specimens from group B which went the same corrosion environment and corrosion time. As can be
seen from the figure, the corrosion of A and B test specimens is increasing with time. However,
under the same conditions, the degree of corrosion in group A was more serious than that in group B.
This shows that greater roughness causes severe corrosion of the surface. When the other conditions
are kept unchanged, and the ambient temperature is set to 40° C and 55° C, the above experiment is
repeated and the same trend is obtained. Figure 3 respectively shows the surface corrosion state of
Group A and Group B specimens observed under a microscope at an corrosion time of 2hour. As can
be seen from the figure, in the same size area, group A had a number of pits of varying sizes and
were independent of each other, while group B had only one pit, showing that group A corrosion was
more severe than group B.
3.2. Potentiometric scan test
Table 3 shows the self-corrosion potential, self-corrosion current density, and corrosion velocity of
aluminum alloys 2A12 with 2 different surface roughness. According to Table 3, at 25°C, as the
surface roughness of the test specimen decreases, the corrosion potential moves positively from -
0.77786 V in group A to -0.73949V in group B,. The corrosion current density decreased from
0.002082 A/cm
2
in group A to 0.002003 cm
2
in group B, indicating that the ion concentration in the
solution decreased, the conductivity decreased, and the corrosion velocity gradually decreased. This
shows that the surface quality has a direct effect on the pitting corrosion of aluminum alloy 2A12,
and the larger the surface roughness is, the easier the pitting corrosion is. In the process of aluminum
alloy corrosion, because of the sensitivity of aluminum to the corrosive medium with chloride ions,
the chloride ions will replace the hydroxides in the aluminum hydroxide sediments by “replacement”
to form highly soluble corrosion product AlCl
3
and falls off from the surface of the substrate.
Corrosion products cannot accumulate for a long time on the surface of the substrate. With the
extension of time, the pits gradually increase, and corrosion solutions accumulate in the pits, which
constitutes a localized micro-electrochemical corrosion environment, which causes the metal in the
pits to continuously undergo anode dissolution. The pits develop simultaneously in both depth and
radial directions. Contact area between the corrosion solution and the metal become larger, and the
corrosion velocity increases. As the corrosion pit expands in the radial direction, adjacent pits will be
connected to each other to form larger pits, destroying the surface integrity of the material. A large
number of pits develop along the depth direction, making the material within a certain depth a porous
material and destroying the continuity of the material. This will inevitably cause a decrease in the
mechanical properties of the material, resulting in a shortened service life and even an abrupt failure.
The above experiment was repeated while maintaining the other conditions unchanged, and the
ambient temperature was set to 40° C. and 55° C. The same change rule of the electrochemical
parameters was obtained.
From Figure 4, it can be seen that the corrosion velocity is increasing with time. However, the
corrosion velocity in group A increased almost linearly, while in group B, the corrosion velocity
hardly changed within the first 4 hours of the onset of corrosion, but it increased linearly after 4
hours. The reason is that the test specimens of group B have small roughness values and have smooth
surfaces and are not prone to corrosion. Therefore, within 4 hours after the corrosion occurs, the
material-medium contact surface caused by the corrosion changes very little and contributes little to
the increase of the corrosion velocity. With the prolongation of time, when the corrosion develops to
a certain extent, pits on the surface of the test specimen increase, the original microroughness of the
material gradually disappears, the effect on the corrosion velocity tend to disappear, and the material-
medium contact surface begins to rapidly increase. As a result, the corrosion velocity rapidly
increases. Therefore, the difference between the corrosion velocity of Groups A and B also continues
to decrease.