Corrosion Flashcards

1
Q

determines whether the reaction is
spontaneous, non-spontaneous or at equilibrium .

A

Gibbs free energy

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1
Q

quantifies the tendency of any
metal’
s to react with its environment.

A

CHANGE OF GIBBS FREE
ENERGY

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2
Q

a simple
“chemical” reaction that can be used to understand how
electrochemical concepts can be applied to predict
corrosion tendency of a metal.

A

Corrosion of iron in an acid

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3
Q

metal atoms lose
electrons and form metal ions

A

Oxidation

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4
Q

non-metallic
substances such as oxygen gain
electron

A

Reduction

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5
Q

overall corrosion reaction can be described in terms of

A

half-reactions

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6
Q

corrosion of metals occurs
within a localized electrochemical
cell

A

corrosion cell.

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7
Q

involves the spatial
separation of anodic and cathodic
areas on the metal surface leading
to formation of corrosion sites.

A

corrosion cell

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8
Q

where oxidation occurs,
leading to the release of metal ions.

A

anode

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9
Q

Reduction reactions take place at
the

A

cathode

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10
Q

serves as a medium
for ion transport

A

electrolyte

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11
Q

the potential difference
measured under standard conditions (1 M concentration, 1 atm
pressure, and a temperature of 25°C) for a half-cell reaction
relative to the SHE.

A

standard electrode potential

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12
Q

quantifies the tendency of a metal to undergo
oxidation or reduction relative to a standard reference electrode

A

standard electrode potential

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13
Q

historically important electrode. It is the halfcell in which hydrogen gas is bubbled over a
platinum electrode immersed in a solution having
a known concentration of hydrogen ions

A

STANDARD HYDROGEN ELECTRODE

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14
Q

On coupling
one of them turns into anodic and the other cathodic such that
the cell potential becomes positive.

A

ELECTRO MOTIVE
FORCE (EMF) SERIES

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15
Q

Hydrogen equilibrium bears

A

zero value

16
Q

most negative or
active half-cell tends to be

A

oxidized

17
Q

most
positive or noble half-cell tends to be

A

reduced

18
Q

Relations between the energy and the potential of a cell

A

NERNST EQUATION

19
Q

outline regions of
active corrosion, oxides/hydroxides
formation, and thermodynamic immunity
for a metal

A

Potential-pH diagrams/Pourbaix diagrams

20
Q

If the oxides/hydroxides protect the underlying metal, then
this region

A

passive region

21
Q

Thermodynamically immune region ensures complete
prevention of metal from corrosio

A

anodic protection and cathodic protection

22
Q

control the cathodic and
anodic currents that are integral components of
corrosion processes

A

polarization effects

23
Q

deviation in
the potential (voltage) of an electrode from its
equilibrium

A

Overpotential

24
Q

quired to
initiate the electrochemical reaction at the electrode
surface.

A

activation energy

25
Q

Activation polarization is due to

A

retarding factors

26
Q

most important
variable that explains the large differences in the rate of
hydrogen production on metallic surfaces.

A

exchange current density

27
Q

often added to power cells
such as the popular alkaline primary
cells to stifle the thermodynamically
favored production of gaseous hydrogen
and prevent unpleasant incidents

A

Mercury

28
Q

provide power in a highly
acidic environment in a relatively safe
manner unless excessive charging
currents are used.

A

lead acid battery

29
Q

arises from the variation in ion
concentrations at the electrode interface

A

CONCENTRATION POLARIZATION

30
Q

related to the mass transport limitations of reactants or
products to or from the electrode surface.

A

CONCENTRATION POLARIZATION

31
Q

When a chemical species participating in a corrosion process is
in short supply, the mass transport of that species to the
corroding surface can

A

become rate limiting

32
Q

Mass transport to a surface is
governed by three forces, that is

A

diffusion, migration, and
convection.

33
Q

The flux of a species O to a surface from the bulk is described with

A

Fick’s first law.

34
Q
A