Ch-5 Compatibility Mode
Ch-5 Compatibility Mode
Ch-5 Compatibility Mode
Chapter 4-
IMPERFECTIONS IN SOLIDS
ISSUES TO ADDRESS...
What are crystal imperfections? What types of defects arise in solids? Can the number and type of defects be varied and controlled? How do defects affect material properties? Are defects undesirable?
Chapter 4- 1
Mechanical properties are often related to the defect structure, with macroscopic failure commonly resulting from a coalescence of damage around existing flaws in a material compact
We have to better understand material structure in order to predict mechanical performance of a material.
Chapter 4-
Chapter 4-
TYPES OF IMPERFECTIONS
Vacancy atoms Interstitial atoms Substitutional atoms Dislocations Grain Boundaries
Foreign particle/ Large Voids/pores/ Non-Cryst regions~10
Chapter 4-
Point defects
(0-D)
Line defects
(1-D)
Area defects
(2-D)
Volume defects
3-D
POINT IMPERFECTIONS
Imperfections of zero dimensions May be created at the time of formation of crystals May be created at a later time due to some thermal disorder They are thermodynamically stable
Chapter 4-
POINT DEFECTS
Vacancies:
-vacant atomic sites in a structure.
Vacancy
distortion of planes
Impurity
Substitutional
Interstitial
Chapter 4- 3
Self-Interstitials:
-"extra" atoms positioned between atomic sites.
distortion of planes
selfinterstitial
Low probability because atoms are substantially larger than the void
Chapter 4-
Defects in Ceramics
Still have interstitials and vacancies
Chapter 4-
Substitutional ions
Chapter 4-
Defect
~e
QD /2 kT
Chapter 4- 7
Na+
Clcation vacancy
initial geometry
ClClO2- impurity
resulting geometry
Chapter 4- 8
Nonstoichiometry
Fe 2+ O 2- Fe 2+ O 2O 2Fe 3+ O 2Fe 2+ O 2-
O 2- Fe 2+ Fe 2+ O 2-
Fe 3+ O 2-
O 2- Fe 2+ O 2- Fe 2+
O 2-
Fe 3+ O 2-
Fe 2+ O 2- Fe 2+ O2Chapter 4-
The variation of Gibbs free energy with the number of point imperfections.
Chapter 4-
Q ND = D exp kT N
Replot it...
ND ln N 1 slope -QD/k
ND N
exponential dependence!
defect concentration
1/T
Chapter 4- 5
For 1m3, N =
Answer:
kT
= 2.7 10
Impurities in Solids
Completely pure metal (or other substance) Impossible!! for 99.9999% - purity still 1022 to 1023 impurities per m3
Chapter 4-
Terminology - Alloys
Solvent component in highest concentration also called host Solute component present in minor concentration
Chapter 4-
OR
Substitutional alloy (e.g., Cu in Ni) Interstitial alloy (e.g., C in Fe)
Solid solution of B in A plus particles of a new phase (usually for a larger amount of B)
Second phase particle --different composition --often different structure.
Chapter 4- 8
Atomic size - < 15% difference Crystal structure same Electro-negativity - ?? Valences more likely to dissolve another metal of higher valence Ag-Au, Cu-Ni, Ge-Si are ideal examples
Chapter 4-
Expect to form solid solution? Ni 3d8 4s2 (28) Cu - 3d10 4s1 (29) Substitutional solid solution
Chapter 4-
Copper-Zinc
Unit cell Zn (HCP) Cu (FCC)
35% of Zn dissolves in Cu where as 1% of Cu dissolves in Zn. The extra bonding electron of Zn is more easily accommodated than a deficiency of bonding electron.
Carbon in Iron
Element Radii Unit cell Electro negativity Valence
Solid solution ? Interstitial or substitional? C - 2s2 2p2 Fe 3d6 4s2
Octahedral void in fcc Fe has radius 0.53 Tetrahedral void in bcc Fe has radius 0.365
Chapter 4-
Specification of Composition of Alloy of 1 and 2 Weight % Atom % C1 = [m1 / m1 + m2] x 100 nm1 = m1/ / A1 C1/ = [nm1 / nm1 + nm2] x 100 C2/ = [nm2 / nm1 + nm2] x 100
Composition conversion:
C1/ = [C1A2 / C1A2 + C2A1] x 100 C2/ = [C2A1 / C1A2 + C2A1] x 100 C1 = [C1/A1 / C1/A1 + C2/A2] x 100 C2 = [C2/A2 / C1/A1 + C2/A2] x 100 C1 + C2 = 100 C1/ + C2/ = 100
Chapter 4-
Wt. % to mass of 1 component / unit volume of material C1// = [C1 / (C1/1) + (C2/2)] x 1000 C2// = [C2 / (C1/1) + (C2/2)] x 1000
ave = [100 / (C1/ 1) + (C2/ 2)] ave = (C1/A1 + C2/A2) / [(C1/A1/ 1) + (C2/A2)/ 2] A ave = [100 / (C1/ A1) + (C2/ A2)] A ave = (C1/A1 + C2/A2) / 100
Chapter 4-
Derivation of composition conversion equation C1/ = [C1A2/(C1A2 + C2A1)] x 100 Total alloy mass : M/ = m1/ + m2/ (in units of grams) C1/ = (nm1/ nm1 + nm2) x 100 = [(m1/ /A1) (m1/ /A1) + (m2/ /A2)] x 100 m1/ = C1M // 100A1 ( since C1 = (m1 / / m1 / + m2 / ) x 100) C1/ = [(C1M // 100A1)(C1M // 100A1+ C2M // 100A2)] x 100 C1/ = (C1A2/C1A2 + C2A1) x 100 Problem: Determine the composition in atom percent of an alloy that consists of 97 wt% Al and 3 wt% Cu
Chapter 4-
CAl/ = {(CAlACu) / (CAlACu + CCuAAl} x 100 = {(97 x 63.55 g/mol) / (97x63.55 g/mol + 3x26.98 g/mol)} x 100 = 98.7 at% CCu/ = {(CCuAAl) / (CAlACu + CCuAAl} x 100 = {(3)(26.98 g/mol) / (3)(26.98 g/mol) + (97)(63.55 g/mol)} x 100 = 1.30 at%
Chapter 4-
LINEAR DEFECTS
Dislocations:
are linear defects,
geometrically one dimensional defect may arise due to incomplete crystal plane or due to plastic deformation crystal undergoes shear part of the crystal is displaced in the direction of the shear due to the shear stress cause slip between crystal plane when they move, produce permanent (plastic) deformation. Boundary between slipped and unslipped region is the line of dislocation
Chapter 4- 11
before deformation
Chapter 4-
Edge dislocations
a
T
Slip vector
Chapter 4-
Chapter 4-
Chapter 4-
To determine the Burgers vector of a dislocation in a twodimensional primitive square lattice, proceed as follows: Trace around the end of the dislocation plane to form a closed loop. Record the number of lattice vectors traveled along each side of the loop (shown here by the numbers in the boxes):
Chapter 4-
Screw dislocation: The dislocation line is parallel to the the slip vector.
Chapter 4-
Screw Dislocation
Chapter 4-
Apply shear
Chapter 4-
Chapter 4-
Mixed Dislocation
Chapter 4-
those of opposite sign cancel each other Dislocations can interact with point imperfections Dislocations usually appear during growth of crystals or as a result of prior mechanical deformation of the crystal. Unlike point imperfections they are not thermodynamically stable They can be removed by proper post treatment
Chapter 4-
Atomic view of edge dislocation motion from left to right as a crystal is sheared.
For metallic materials, b will point in A close-packed crystallograhic direction and will be of magnitude Chapter 4- 13 Equal to interatomic spacing.
Chapter 4-
AREA DEFECTS
2 D imperfections Regions of distortions that lie on the surface or grain boundaries having a layer of thickness of a few Surface atoms are bonded to less nearest neighbours as compared to coordination numbers. Hence they are at higher energy state compared to atoms in the interior. The broken bonds of these atoms give rise to surface energy.
Chapter 4-
grain boundaries
heat flow
Angle of misalignment
Chapter 4-
Area Defects
Tilt Boundary array of edge defects Twin Boundary
Twist Boundary array of screw defects (atleast 2 sets of parallel screw dislocation)
Chapter 4-
Twin Boundaries
A twin boundary is a special type of grain boundary across which there is a specific mirror lattice symmetry. Atoms on one side of the boundary are located in mirror-image positions of the atoms on the other side. The region of material between these boundaries is termed a twin.
Chapter 4-
Twin Boundary
Twinned region
Twin boundaries
Chapter 4-
ABCABCABABCABC Stacking fault is a thin region of hcp in fcc lattice. ABCACBCA Twin stacking fault Bulk defects like pores, cracks etc during process occur
Atomic vibrations Not all atoms vibrate with same energy, distribution of energies Chapter 4present.
Adapted from Fig. 4.11(b) and (c), Callister 6e. (Fig. 4.11(c) is courtesy of J.E. Burke, General Electric Co.
0.75mm
Chapter 4- 16
N = 2n-1
no. grains/in2 at 100x magnification
Fe-Cr alloy
Chapter 4- 17
SUMMARY
Point, Line, and Area defects arise in solids. The number and type of defects can be varied and controlled (e.g., T controls vacancy conc.) Defects affect material properties (e.g., grain boundaries control crystal slip). Defects may be desirable or undesirable
(e.g., dislocations may be good or bad, depending on whether plastic deformation is desirable or not.)
Chapter 4- 18
C
Chapter 4-
Mixed dislocation
Edge dislocation
Screw dislocation
Chapter 4-