Corrosion 6 Flashcards

1
Q

is also
known as general corrosion. A
type of corrosion where the
corroded areas occur in a
manner evenly distributed
across the material being
attacked.

A

Uniform corrosion

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2
Q

is a primary cause of
uniform corrosion in steels,
alloys, and other metals in
natural environments.

A

Oxygen

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3
Q

is
also known as
intergranular attack (IGA).
This is a specialized type of
attack that takes place at
the grain boundaries of a
metal.

A

Intergranular corrosion

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4
Q

This form of corrosion is
often caused by impurities
in the metal, leading to
chemical or
electrochemical attack on
the grain boundaries.

A

INTERGRANULAR CORROSION

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5
Q

is also known
as dissimilar metal corrosion or
bimetallic corrosion. When two
different metallic
materials are electrically
connected and placed in a
conductive solution (electrolyte),
an electric potential exists.

A

Galvanic corrosion

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6
Q

is a
localized type of corrosion
occurring within or adjacent
to narrow gaps.

A

Crevice corrosion

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7
Q

is
characterized by a highly
localized loss of metal. The
initiation of a pit is associated
with the breakdown of the
protective film on the metal
surface

A

Pitting corrosion

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8
Q

is
usually caused by an
aqueous or gaseous
corrodent flowing over
the metal surface or
impinging upon it.

A

Erosion corrosion

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9
Q

is a phenomenon where cracks
form and propagate in a
material due to the combined
effects of sustained tensile
stress and exposure to a
corrosive environment.

A

Stress corrosion cracking

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10
Q

refers to the
degradation of metals caused
by the activity of living
organisms. This is also referred
to as microbial-induced
corrosion (MIC).

A

Biologically influenced
corrosion

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11
Q

is the term to
describe the leaching of zinc
from brass.

A

Dezincification

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12
Q

is the term
used to describe the selective
leaching of iron from gray cast
iron.

A

Graphite corrosion

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13
Q

When intergranular corrosion
takes place in a metal with a
highly directional grain structure,
it propagates internally, parallel
to the surface of the metal.

A

EXFOLIATION

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14
Q

is the cracking of a
metal or alloy under the combined
action of a corrosive environment and
repeated or fluctuating stress.

A

Corrosion fatigue

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15
Q

is when metals and
alloys fail by cracking when subjected
to cyclic or repetitive stress

A

Fatigue failure

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16
Q

The growth formation is explained by the
formation of a differential aeration cell

A

FILIFORM CORROSION

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17
Q

the process
of a metal returning to
the material’s
thermodynamic stat

A

Corrosion

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18
Q

The measure of the potential
difference between two half
cells in an electrochemical cell

A

Cell Potential

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19
Q

may be formed when two
dissimilar metals are in
contact or due to the
heterogeneity of the
same metal surface

A

Dissimilar electrode cells

20
Q

are
formed when the
electrodes are identical
but are in contact with
solutions of differing
composition

A

Concentration cells

21
Q

Formed when electrodes
of the same metal, each of
which is at a different
temperature, are
immersed in an
electrolyte of the same
initial composition

A

DIFFERENTIAL TEMPERATURE CELL

22
Q

This situation arises when
a significant difference in
metal ion concentration
exists over ametal
surface

A

METAL ION CONCENTRATION CELLS

23
Q

Also knownas Pourbaix Diagram

A

Potential-Ph Diagrams

24
Q

Constructed from calculations
based on the Nernst equation and
the solubility data for various
metal compounds

A

Potential-Ph Diagrams

25
Under these condition of potential and pH, the metal remains in metallic form and is free from corrosion
Immunity Zone
26
Under these condition of potential and pH, the metal corrodes
Corrosion Zone
27
Under these condition of potential and pH, protective layer of the metal's hydroxide or oxide form on iron and further corrosion of metal doesn’t take place
Passive zone
28
The potential change caused by net current to or from an electrode, measured in volts
POLARIZATION
29
is a manifestation of the relative changes in the activation energies for dissolution and deposition, when equilibrium is disturbed.
Activation polarization
30
Polarization of an electrolytic cell resulting from changes in the electrolyte concentration due to the passage of current through the electrode/solution interface
Concentration Polarization
31
The change in voltage associated with effects of the environment and the circuit between the anode and cathode sites. It includes the effects of the resistivity of the media, surface films, corrosion products, etc.
Resistance Polarization
32
is a complicated electrochemical process taking place in corrosion cells consisting of base metal, metallic corrosion products, surface electrolytes, and the atmosphere
Atmospheric corrosion
33
is negligible in climates where the air temperature is below the freezing point of water because ice is a poor conductor and does not function effectively as an electrolyte
Rusting
34
refers to the length of time during which the metal surface is covered by a film of water
Time of wetness
35
The amount of water adsorbed on a metal surface depends on the relative humidity of the atmosphere and on the chemical and physical properties of the corrosion products.
Adsorption Layers
36
Occurs when the temperature of the metal surface is below the dew point of the atmosphere
Dew
37
creates even thicker layers of electrolyte on the surface than dew. It affects corrosion by adding a phase layer of moisture and corrosion stimulators.
Rain
38
high acidity and high concentrations of sulfates and nitrate can be found in fog droplets in areas of high air pollution
Fog
39
can promote corrosion because of their hygroscopic nature
Dust
40
on the surface will contain various species deposited from the atmosphere or originating from the corroding metal.
electrolyte film
41
The metal is covered with a spontaneously formed oxide and aqueous layer
INDUCTION PERIOD
42
The oxide layer transforms into a fully developed layer of corrosion products
TRANSITION PERIOD
43
The surface being fully covered by corrosion product and reach constant corrosion rate
STATIONARY PERIOD
44
defined as the ratio of deposition rate of any gaseous compound and the concentration of that compound in the atmosphere
dry deposition velocity
45
When small amounts of copper, chromium, nickel, etc. are added to carbon steel, low-alloy carbon steel results. These steels are known as
weathering steels