T3-6: Basic Principles of Corrosion Flashcards

(33 cards)

1
Q

Name three global implications of corrosion

A
  • More CO2 emissions (new steel, cement, zinc, paints; transport, removal)
  • Use of more natural resources (iron ore, lime stone, coal)
  • Reduced recyclability
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2
Q

Name six local implications of corrosion

A
  • Reduced operational life
  • Safety risk
  • Costs (both environmental and financial)
  • Maintenance down time
  • Impact on traffic flow; pollution
  • Higher whole life cost
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3
Q

Define corrosion

A

A reaction between a refined metal and the environment

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4
Q

What are the causes (x2) of corrosion?

A
  • Metal loss/degradation
  • Modification of the environment (pH, ions, etc)
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5
Q

[NAQ] simple energy diagram for corrosion

A

Metal has highest energy after refining energy is applied, and before corrosion causes energy out

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6
Q

Describe the process from metals as ores to refined metals

A
  • Engineering metal exist as ore (low energy, very poor mechanical properties)
  • The ore is refined to improve mechanical properties; adding energy
  • The refined metal is a loaded energy source
  • The “right conditions energy” is released
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7
Q

What are the four elements needed for corrosion to occur?

A
  • Anode
  • Cathode
  • Metallic bridge
  • Electrolyte
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8
Q

What is the role of the anode in a corrosion cell?

What occurs at the anode?

Name the equation

A
  • The anode is the site where oxidation (loss of electrons) occurs, leading to metal dissolution and the formation of metal ions, which then migrate to the cathode
  • Energy production (metal lost to environment)
  • Anode = high electrode potential site; ionisation occurs

Metal → Energy + Metal with less energy (m → e- + m2+)

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9
Q

What is the role of the cathode in a corrosion cell?

What occurs at the cathode?

What is developed and how does the pH change?

Name the equation

A
  • The cathode is the site where reduction occurs, receiving electrons from the anode and preventing corrosion at that location
  • Consumption of energy
  • Energy generated by anode accumulates on the surface - develops hydroxide - pH becomes more alkaline
  • Cathode = lower electrode potential site; electrons flow through electrolyte to cathode (combine with water and oxygen)

Environment + Energy → Environment uses up energy and produces new product

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10
Q

What is the role of the metallic bridge in a corrosion cell?

A
  • Energy transport
  • Facilitates the flow of electrons between the anode (where oxidation occurs) and the cathode (where reduction occurs), thus completing the electrical circuit and enabling the corrosion process
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11
Q

What is the role of the electrolyte in a corrosion cell?

What does it act as?

A
  • Transport of reactants to the surface
  • Removal of products from the surface
  • Acts as a conductive medium, enabling the flow of ions (charge carriers) between the anode and cathode, facilitating the electrochemical reactions that drive corrosion
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12
Q

How can you prevent electrolytes from reaching the surface?

A

Paint the structure

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13
Q

How is steel normally protected against corrosion in (uncontaminated) concrete?

What is formed?

A
  • Cement hydration produces large quantities of calcium, sodium and potassium hydroxides, leading to high pH
  • This promotes the formation of passive oxide layers, which prevent further corrosion
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14
Q

What pH promotes the formation of passive oxide layers, for protection against corrosion?

Is this a low or high pH?

A

pH 12.5 to 13.5

High pH

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15
Q

How do the following uncontaminated concrete elements protect against corrosion?

a) Uncracked concrete (what name is given?)
b) Steel reinforcement

A

a) Restricts movement and access of chlorides and CO2 - diffusion controlled migration

b) The passive oxide layer (if intact) prevents further corrosion of reinforcement

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16
Q

What are the metal states at the different parts (A-D) of the potential-pH diagram for iron in water?

A

A - Corrosion
B - Immunity (metal is thermodynamically stable and doesn’t corrode)
C - Passivity (metal forms a protective layer on its surface that inhibits further corrosion)
D - Corrosion

17
Q

What are the two main concrete deterioration processes?

A
  • Chloride-induced corrosion
  • Carbonation
18
Q

Describe the main steps (x3) of chloride-induced corrosion of steel in concrete?

A
  • Chloride contamination leads to a loss of the protective oxide layers
  • Corrosion initiates once a critical chloride level occurs at the steel surface
  • Very localised pitting corrosion and section loss can occur
19
Q

[NAQ] chloride-induced pitting corrosion of steel in concrete

What is the active pit zone pH?

A

Concrete pH>12.15
Active pit zone pH<5

20
Q

What is the impact of chloride-induced pitting corrosion of steel in concrete?

A
  • Presence of chloride-ions leads to localised ‘pitting’ corrosion
  • Common to have significant section loss of rebar
  • This impacts tensile capacity
21
Q

Describe the main steps (x3) of carbonation-induced corrosion of steel in concrete

What does the CO2 from the atmoshphere do?

A
  • The passive films rely entirely on the pH; any drop in pH will lead to the breakdown of this film and initiation of corrosion
  • CO2 from the atmosphere can react with the free OH- (hydroxide) within the concrete; lowering the pH of the pore water
  • General corrosion occurs; leading to uniform loss of metal (typical of general atmospheric corrosion)
22
Q

[NAQ] diagram of carbonation-induced corrosion

A

Concrete pH>12.5

23
Q

[NAQ] potential-pH diagram for iron in water, showing movement from passivity to corrosion state

24
Q

What is the impact of carbonation-induced corrosion of steel in concrete?

What can happen in ‘extreme cases’?

A
  • The loss of pH leads to general corrosion
  • Section loss in extreme cases is tapered, due to general section loss following loss of protective concrete cover
25
What is the impact of corrosion of steel in concrete with O2? What forms as a result, and why?
- O2 available (concrete - wet and dry) - **Expansive forces** and **expansive corrosion product** occur - **Cover concrete cracks form** to **relieve pressure build up** from the expansive corrosion product
26
What causes a loss of tensile capacity and what causes a loss of compressive strength, due to corrosion?
Loss of **tensile** capacity from **reinforcing steel section loss** Loss of **compressive** strength from **cover concrete cracks**
27
What is the impact of corrosion of steel in concrete without O2? What forms as a result?
- **No** **O2 in water saturated** concrete - **Non-expansive corrosion product forms** on top of chloride-induced pitting corrosion - The corrosion product **leaches out of concrete as a soluble by-product** - The cover concrete is **stained but not cracked**; hammer survey does not indicate damaged concrete
28
What provides corrosion protection to steel in concrete?
The high pH (hydroxide content)
29
Describe the difference between chloride-induced corrosion and carbonation
- **Chlorides don't change the pH**, but compete with the hydroxide and **perforate the passive oxide layer**; causing **pitting** - In carbonation, **carbon dioxide neutralises the hydroxide and lowers the pH** to levels where the **passive oxide is no longer stable**; causing generalised corrosion
30
What do expansive corrosion products cause?
Expansive corrosion products (rust) **crack** the cover concrete, then normal aqueous corrosion continues
31
Name three design factors
1. **Asset life** - **predicted** design life, based on **concrete cover** and **diffusion ratio** - **actual** design life based on build quality, exposure conditions, etc 2. **Buildability** - **concrete cover required** - even with PFA and GGBS it only works if it is crack-free 3. **Corrosion risk** - corrosion **control options** needed at design stage, based on **exposure conditions** - anticipate construction faults, life extension requirement, changes to purpose of use
32
Why is concrete cover required?
For **pH and diffusion control** of **chlorides and CO2**
33
Why can pitting lead to a rapid loss of tensile capacity?
- Once pitting corrosion starts it is **difficult to stop** - **Pit zone** continues to **attract chlorides** - Pitting corrosion is very localised and leads to **tensile capacity being lost** very quickly