Chapter 10: Corrosion Flashcards

1
Q

Corrosion

A

Destructive attack of a metal by electrochemical interaction or chemical reaction with its environment.

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2
Q

Corrosion conditions (2)

A

The presence of an oxidizing agent (O2, CO2, H2O) and a reducing agent (metal being corroded). The reaction must be thermodynamically favorable.

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3
Q

Oxidization

A

Loss of electrons at the anode (LEO)

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4
Q

Reduction

A

Gain of electron at the cathode (GER)

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5
Q

Oxidizing agent

A

A chemical compound that readily transfers oxygen atoms that gains electrons in a redox chemical reaction. It is reduced.

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6
Q

Reducing agent

A

A chemical compound that readily donates electrons in a redox chemical reaction. It is oxidized.

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7
Q

Rust on steel

A
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8
Q

Components of an electrochemical (galvanic) cell (4)

A

Anode, cathode, electrical connection, electrolyte

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9
Q

Anode

A

Gives up electrons and produces ions (cations). Is the reducing agent that undergoes oxidation.

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10
Q

Cathode

A

Accepts electrons and consumes ions (cations) Is the oxidizing agent that undergoes reduction. Is rich in anions (at surface)

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11
Q

Electrical connection

A

Connects and allows electrons to flow from the anode to the cathode.

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12
Q

Electrolyte

A

Conducts current from the cathode to the anode. Must be in contact with anode and cathode.

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13
Q

Standard conditions

A

25°C,1.0M concentration of ions in the electrolyte solution, and 1atm.

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14
Q

Electrochemical potential equation

A

ΔVo = Vcathode - Vanode

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15
Q

Spontaneous reaction voltage sign

A

Positive voltage

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16
Q

Non-spontaneous reaction

A

Negative voltage

17
Q

Electrochemical potential

A

Helps decide where the anode is (where corrosion occurs)

18
Q

Effect of concentration on potential

A

The higher the concentration of the cation species, the more cathodic (+) the potential.
V = Vo - 0.0592/n*log(1/Cion)
If C < 1, V is more negative

19
Q

Faraday’s law

A

The total weight of metal oxidized at the anode.

20
Q

Faraday’s Law formula

A

w = ItM/nF
I = corrosion current (A)
t = time (s)
M = molar mass (g/mol)
n = valence electrons
F = Faraday constant

21
Q

Corrosion penetration rate

A

CPR = KW/pAt (mm/yr)
K = constant
W = weight loss
p = density
A = exposed area
t = time

22
Q

Corrosion rate

A

r = i/nF (mol/m^2s)
i = current density (A/m^2)
n = electrons associated with ionization
F = Faraday constant

23
Q

Types of corrosion (5)

A

Uniform attack, galvanic corrosion, crevice corrosion, pitting corrosion, intergranular corrosion

24
Q

Uniform attack

A

Corrosion attack is of uniform intensity throughout the part (EX: silverware tarnishing).

25
Q

Galvanic Corrosion

A

When two dissimilar metals are in contact with an electrolyte. Less noble metal corrodes (EX: plumbing does not connect stat to tubing).

26
Q

Crevice Corrosion

A

Corrosion, which occurs because of differences in concentration of a solution is usually because of stagnant flow conditions in a crevice.

27
Q

Pitting corrosion

A

Cause similar to crevice corrosion. Pits form on surface of material

28
Q

Intergranular corrosion

A

Corrosion occurs in preferential mode in the structure of the material. Caused by processing, impurities or welding

29
Q

Stress Cell

A

Stressed area has a higher free energy and becomes the anode. Tensile stress accelerates corrosion, whereas compressive stress slows corrosion.

30
Q

Concentration cell

A

A dissolved species involved in either the anode or cathode reaction varies in concentration at different locations in the electrolyte.

31
Q

Corrosion control methods (6)

A
  1. Coatings
  2. Inhibitors
  3. Reduce dissolved oxygen
  4. Galvanic protection
  5. Cathodic protection
  6. Reducing temperature
32
Q

Coatings and Inhibitors

A

Coating the surface to isolate it from the electrolyte and/or make adherent ions that coat the surface and isolate it from the electrochemical reaction. These methods must be replenished periodically.

33
Q

Reducing dissolved oxygen

A

Inhibiting corrosion by adding hydrazine to water or treating the water using a hydrogen protection cell that replaces the oxygen in the water with hydrogen.

34
Q

Galvanic protection

A

Where a more anodic metal is hooked up to the metal to be protected and dipped in the electrolyte. Commonly used in metal ships.

35
Q

Cathodic protection

A

A small DC voltage is used to impress electrons into the steel, rendering the metal cathodic. This is used in addition to protective coatings.