Corrosion 4 Flashcards

1
Q

term used to describe this reduction, denoted as ΔG

A

Reaction affinity

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2
Q

a quantitative measure of a chemical reaction’s tendency to start, which includes the reaction of a metallic material with its environment.

A

Gibbs free energy change (ΔG)

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3
Q
  • a direct measure of the work capacity or the maximum electric energy possible that is available from a system.
A

Gibbs free energy change (ΔG)

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4
Q

said to be lost and a spontaneous reaction direction of the system is observed.

A

negative free energy

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5
Q

change means that the transition indicates an energy increase, and it requires additional energy to be added to the system.

A

positive value of Gibbs free energy

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6
Q

can be classified as a state function and is independent of the reaction path.

A

change in free energy

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7
Q

can be defined as a product of charges moved (Q) and the electrochemical potential (E) through which it is moved.

A

electrical work (w)

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8
Q

crucial part of the corrosion process, can be used to express the tendency of a metal to corrode.

A

electromotive force (emf)

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9
Q

higher tendency for the overall chemical reaction of the cell to proceed

A

higher value of E

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10
Q

larger tendency to make the reaction proceed.

A

More negative value of ΔG

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11
Q

value refers to a reaction that has no tendency to start at all.

A

positive ΔG°

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12
Q

For a reaction to take place, the driving voltage must be

A

positive.

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13
Q

ΔG = 0, ΔG > 0

A

reaction might not occur

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14
Q

system is more likely to change in the other direction to that stated.

A

when ΔG > 0,

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15
Q

activity coefficient

A

dissolved species

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16
Q

fugacity coefficient

A

gaseous species

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17
Q

the tendency of a material to corrode is not a direct measure of reaction rate.

A

true

18
Q

The standard conditions for solid, liquid compounds, and even elements is the pure compound or element; in the case of gases, it is set at a pressure of

A

100 kPa and for solutes, the ideal concentration is 1 M (mol/L).

19
Q

equilibrium electrodes are also termed

A

half-cells

20
Q

”. If these electrodes are maintained at equilibrium conditions, they are now called

A

standard half-cells

21
Q

an equation can be derived to determine the emf of a certain cell by virtue of the reactants and products’ concentration.

A

The Nernst Equation

22
Q

used to determine the potential of a system wherein the reactants are not in unit activity.

A

Nernst equation

23
Q

study of reaction rates at the interface between an electrode and a liquid.

A

Electrode Kinetics

24
Q

The deviation from equilibrium potential is called

A

polarization

25
Q

measurement of magnitude of polarization with respect to the equilibrium potential of an electrode.

A

Overvoltage

26
Q

electrochemical process that is controlled by the reaction sequence at the metal-electrolyte interface.

A

Activation Polarization

27
Q

usually is the controlling factor during corrosion in media containing a high concentration of active species.

A

Activation Polarization

28
Q

generally predominates when the concentration of the reducible species is small.

A

Concentration polarization

29
Q
  • electrochemical reactions that are controlled by the diffusion in the electrolyte.
A

Concentration polarization

30
Q

polarization can lead to the formation of a protective oxide layer on the metal’ s surface which acts as a barrier, slowing down further corrosion.

A

Passivation

31
Q

polarization can also increase corrosion rates by promoting more aggressive electrochemical reactions. This can happen if conditions favor the dissolution of the protective oxide layer.

A

Increased Corrosion

32
Q

polarization gradients within the metal surface can lead to the concentration of corrosive agents in specific areas, accelerating corrosion rates locally.

A

Localized Corrosion

33
Q

amount of current (I) over a given area (A)
- The total charge that passes through the cell when N moles of the metal M react is Q.

A

CURRENT DENSITY

34
Q

a model for the current density of an electrode when the only significant limiting factor is activation.

A

tafel equation

35
Q

uniformly over the entire exposed surface.
- does not create a great concern, because the life of equipment can be accurately estimated on the basis of comparatively simple tests.

A

Uniform Corrosion

36
Q

Metal deterioration that happens in tight spaces where a stagnant liquid gets trapped.

A

Crevice Corrosion

37
Q
  • A highly localized form of attack that eats away at the metal, creating small holes or cavities.
A

Pitting Corrosion

38
Q

Due to chemical composition difference at the grain boundaries from the bulk of the grain.

A
39
Q

two dissimilar metals with potential difference in a conductive solution.
- s a serious threat because it accelerates the deterioration of the less resistant metal.

A

Galvanic Corrosion

40
Q

Degradation that occurs when hydrogen penetrates the surface of a metal.

A

Hydrogen Damage

41
Q
A
42
Q
A