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1. Group Discussion: It is said that corrosion is a natural phenomenon. Explain the context
and implications of this statement. Can corrosion be used to our benefit? Give an example
if you think so.
2. For design engineers and corrosion engineers it is important to determine the corrosion rate.
One way of determining corrosion rate is to measure the weight loss of a sample coupon
over a period of time submerged in a corroding medium.
(a) Group Discussion: Design an immersion test for a carbon steel in seawater:
describe sample specification and preparation; describe test procedure and
conditions, describe what to measure and how to obtain the data.
(b) Individual Work: Derive an expression of the rate of corrosion in mmpy using data
from such a measurement. (Identify every variable in your equations).
(c) Individual Work: A piece of uncoated low carbon steel plate coupon of 40 10 2
mm was measured to have lost 5.4 g after exposure in a production pipeline for 3
months. Determine the rate of corrosion in mmpy.
Additional Question
5. The company plans to produce a new printed circuit heat exchanger using SS3016L, and
needs to determine the time required for chemical etching. The heat exchange passage are
designed to have 3 x 1 mm cross section. The task is given to you. How would you do it?
http://www.heatric.com/typical_characteristics_of_PCHEs.html
1. Individual Work: Another way to determine corrosion rate is to measure the current
discharged from a corroding metal. A metal, M, of valence z, atomic mass W and density
D (kgm-3) is corroding uniformly over its exposed surface by an electrochemical process
with a current density of icorr (Am-2).
(a) Derive an expression of corrosion rate in mmpy of the metal, assuming that the build-
up of corrosion product does not affect the corrosion reaction.
(b) If the metal is Cu and the corrosion current density is 0.01 Am-2, calculate the
corrosion rate. (0.0116 mmpy)
(c) Group Discussion: Discuss the similarities and differences between this method and
the coupon weight loss method.
2. Group Discussion: Explain why crevice corrosion is considered autocatalytic. Explain
why it is accelerated by the migration of Cl- into the crevice. Explain why it is said to be
particularly difficult to detect. Does the above also apply to pitting corrosion?
3. Group Discussion: Two plates of mild steel are bolted together by a plastic bolt, forming
a small gap between them. Explain what is likely to happen within the gap if the pair is
placed in
(a) neutral water
(b) seawater
(c) If the plates are austenitic stainless steel, what is likely to happen?
4. Group Discussion: What is the sensitisation of austenitic stainless steels? What are the
typical conditions that cause sensitisation? Can it be avoided? Once happened, can it be
eliminated?
5. Individual Work: You are required to
design a small stainless steel pipe flange
fitting that requires welding. The pipe and
flange are made of type 304 steel. What
should you consider in terms of corrosion?
Would using type 347 welding rod resolve
the issue? If not, make your
recommendation.
4. Individual Work: Calculate the Pilling Bedworth ratio of Al2O3 (you may request any
information you need)
1. Electrochemical corrosion occurs always with concurrent anodic and cathodic reactions.
Whereas there are many different anodic reactions depending on the corroding metal,
there are five generic cathodic reactions. Please write out the five common cathodic
reactions.
2. Write the possible oxidation and reduction half-cell reactions that occur when a piece of
Mg is immersed in each of the following media: (i) de-aerated HCl aqueous solution, (ii)
HCl aqueous solution containing dissolved oxygen, (iii) HCl aqueous solution containing
dissolved oxygen and Fe+2 ions. In which of these solutions would you expect the
magnesium to oxidize most rapidly? Why?
3. Assuming standard states for all reactants and products,
(a) Determine the spontaneous direction of the following reaction by calculating the cell
potential: Cu + 2HCl = CuCl2 + H2
(b) Define the standard state for each reactants and products
4. A galvanic cell at 25°C consists of an electrode of zinc in a 0.1M ZnSO4 solution and
another electrode of nickel in a 0.05M NiSO4 solution. The two electrodes are separated
by a porous membrane. What is the driving force (the potential) of the cell? [Ecell =
0.504 V]
5. Group Discussion:
(a) What is an E/pH diagram
(Pourbaix diagram)?
(b) What can Pourbaix diagrams
do and cannot do?
(c) What do the parallel lines
mean?
(d) Identify the regions where Fe
is not corroding.
(e) What will be the status of iron
if it is immersed in an aqueous
solution of 10-4 M [H+]
concentration or 10-13 M [H+]
concentration?
(f) What will happen if you put a
piece of 1020 steel in coca
cola?
3. Explain the concept of exchange current density. Figure 3 shows exchange current
densities of the same hydrogen electrode on different metal substrates. Explain the
information presented in the figure (e.g., what does 𝑖𝑜 (Fe) mean relative to 𝑖𝑜 (Pt)).
Can you prove the linear relationship between overpotential and current density? (hint:
this is activation polarization, and the law of activation is expressed by Arrhenius
equation) (Solution is given in lecture ppt)
4. What would happen to the corrosion rates in the question above if:
(a) the acid solution was stirred?
(b) the temperature of the solution was increased?
(c) the concentration of the acid was increased?
5. Calculate the free energy change ∆𝐺𝑜 for iron oxidation to Fe2+ under standard conditions.
(-84.9 kJ mol-1)
6. A common impurity in commercial hydrochloric acid (HCl) is ferric ion Fe+3, present as
ferric chloride, FeCl3. Using a schematic E vs log i diagram to illustrate the corrosion of an
active metal (e.g., mild steel coupon) immersed in a dilute HCl solution contaminated by
ferric chloride. On the diagram, find the corrosion rate icorr and corrosion potential Ecorr.
Compare the corrosion rate of this metal when the ferric ions are absent in the solution to
that when the ferric ions are present. Can you explain the main cause of the decreased
hydrogen evolution when the ferric ions are present?
Most questions of this tutorial requires no further explanation beyond the lectures, except
question 6. They are offered to help with your study and revision of chapter 4.
2. How is crevice corrosion tested and how is crevice corrosion tendency of a material
evaluated?
3. Comment on the methods used to evaluate the tendency of pitting corrosion.
4. What are the main techniques for stress corrosion cracking testing? Comment briefly on
their main differences.
5. How is sensitization of stainless steels tested?
6. In an electrochemical testing of lead (Pb) in a dilute acid solution, it is found that the
potential applied to it and the current density generated by its corrosion follow a linear
∆𝐸 𝑚𝑉
relationship with a slope of ∆𝑖 = 0.72 (𝑚𝐴/𝑐𝑚2 ). The Tafel constants of the Pb/Pb+2
electrode and the H/H+ electrode in the solution are determined to be Pb/Pb+2 = 0.12 and
+
H/H = - 0.10. Estimate the self-corrosion rate of Pb under this condition.
Most questions of this tutorial requires no further explanation beyond the lectures, except
question 6. They are offered to help with your study and revision of chapter 4.
--------------
Saturated calomel electrode (Hg-Hg2Cl2, SCE): E = +0.244 V
Cu-CuSO4 electrode: E = +0.314 V
Saturated Ag-AgCl electrode: E = +0.197 V
1. Calculate the theoretical capacity of zinc sacrificial anode material. The measured capacity
of a zinc anode is 780 Ahkg-1. Calculate the efficiency of the metal as a sacrificial anode.
Calculate the consumption rate of the zinc anode. (819 Ahkg-1)
3. Self-investigation: There are three common sacrificial anode materials: Zn, Al and Mg.
Comment on which, or if all, is suitable for use in seawater.
6. You are asked to design a sacrificial anode cathodic protection system for a subsea
structure. What information would you need?
http://dynamicdivers.gr/wpcontent/gallery/anodeswelding/dynamic_divers00003.jpg
1. The figure below shows a schematic of an impressed current cathodic protection system
using an overhead power line.
(1) Explain the function of the rectifier.
(2) Determine the connection polarity to the pipeline and the anode.
(3) Explain what the anode is made off.
pipe
d
anode
D
3. The figure below shows corrosion protection monitoring using a saturated Ag/AgCl
reference electrode of an underwater carbon steel structure protected by sacrificial anode.
The case with a reading of -0.6 V is considered under-protected (not properly protected)
and the case with reading of -0.95 V is considered fully protected. Explain why.
5. Discuss the electrical current consumptions of ICCP under three conditions: under-
protected; protected and over-protected (graphically).