MCQ V - Raghavan - Materials - Science - and
MCQ V - Raghavan - Materials - Science - and
starting from room temperature required to double the reaction rate for a
value of Q equal to (i) 100 kJ mol–l and (ii) 200 kJ mol–l.
Answer: (i) ~5°C, (ii) ~2.5°C.
2.7 Find the activation energy from an Arrhenius plot for a reaction that
requires the following times for completion at the indicated temperatures:
Temperature, K Time, s
600 9360
700 27.5
800 0.73
900 0.01
Answer: ~200 kJ mol–l.
2.8 A reaction takes 500 min at 10°C for completion. It takes 1 min at 80°C.
Find the time it would take at 40°C.
Answer: 25 min.
2.9 The vibrations of atoms in a solid can be considered as elastic waves. The
limiting wavelength of the elastic waves can be taken to be the interatomic
spacing, which has a value of about 10–10 m. Estimate in order of
magnitude the velocity of elastic waves in a solid above room temperature.
Answer: 1 km s–l.
2.10 In Eq. (2.12), show that (dDS/dn) ® ¥, as n ® 0. Explain why it is very
difficult to remove the last traces of impurities during purification of a
material.
2.11 A reaction with activation energy equal to 100 kJ mol–l takes 50 min for
completion at 300 K. At what temperature will it be complete in 5 min?
Answer: 318.3 K.
Answers
1. B 2. C 3. A 4. D 5. A
6. A 7. B 8. D 9. C 10. A
11. C 12. C 13. D
Problems/Multiple Choice Questions 49
3.29 Explain with a neat sketch why a (100) reflection is not possible from an
FCC crystal.
3.30 A Debye-Scherrer pattern is obtained from an FCC crystal with
a = 3.61 Å. X-rays of wavelength equal to 1.54 Å are used. Determine the
Miller indices of the planes with the lowest and the highest Bragg angles
in this pattern.
Answer: {111} and {420}.
3.31 Only two reflections are observed on the powder pattern of a cubic crystal
at Bragg angles of 34.06° and 65.51°. Chromium Ka radiation is used.
Determine the crystal structure (if possible) and the lattice parameter.
Show that the third and higher reflections cannot occur.
Answer: DC, 3.56 Å.
3.32 The entry point and the exit point of x-rays on a powder pattern taken
from a cubic material could not be distinguished. Assuming one of the
points to be the exit point, the following S values were obtained: 311.95,
319.10 and 335.05 mm. The camera radius is 57.3 mm. Molybdenum Ka
radiation was used. Determine the structure and the lattice parameter of the
material.
Answer: DC, 5.66 Å.
3.33 The first two reflections as seen in the powder photograph of a cubic
material have S values of 90.1 and 154.7 mm, respectively. As the film
between these two reflections was torn, it was not clear whether an
additional line was present between the two observed lines. Determine, if
possible, the crystal structure and the lattice parameter. The third and the
fourth reflections as seen in the torn film have S values of 188.4 and
199.8 mm. The camera radius is 57.3 mm. Cobalt Ka radiation was used.
Answer: FCC, 4.05 Å.
3.34 In the damaged powder film of a cubic material, the locations of only the
first two pairs of lines could be accurately measured. They had S values of
24.95 and 40.9 mm. The camera radius is 57.3 mm. Molybdenum Ka
radiation was used. If possible, determine the crystal structure and the
lattice parameter of the material. The third pair of lines in the damaged
film was estimated to have an S value of about 49 mm. Determine whether
this confirms your conclusion or not.
Answer: DC, 5.66 Å.
1. The space lattices with two lattice parameters belong to the crystal systems
A. tetragonal B. rhombohedral C. hexagonal D. triclinic
50 Multiple Choice Questions
15. The angle between [111] and [112] directions in a cubic crystal is
A. 0° B. 45° C. 90° D. 180°
16. The number of members in the family <123> in a cubic crystal are
A. 8 B. 12 C. 24 D. 48
17. The (1 11) plane is parallel to
A. (111) B. (11 1) C. (1 11) D. (11 1)
18. The Miller indices of a plane in an orthorhombic unit cell (a : b : c =
1 : 2 : 3) making intercepts of 3, 2, 1 Å on a, b, c, axes are
A. (931) B. (139) C. (321) D. (123)
19. The four non-parallel body diagonals of a cube have Miller indices
A. [111], [111], [1 11], [11 1] B. [111], [1 1 1], [1 11], [11 1]
C. [1 1 1], [1 1 1], [11 1], [1 11] D. [1 11], [11 1], [1 11], [111]
20. The Miller indices of the line of intersection of a (1 11) and a (1 10)
plane are
A. [1 10] B. [110] C. [1 10] D. [1 11]
21. If the interplanar spacing obtained from the second reflection of a DC
crystal is 1.81 Å, the lattice parameter is
A. 0.905 Å B. 2.56 Å C. 3.62 Å D. 5.12 Å
22. The first S value on the powder pattern of an FCC crystal (a = 4.05 Å)
taken with a camera of radius 57.3 mm using cobalt Ka radiation of
1.79 Å is
A. 45 mm B. 51 mm C. 72.8 mm D. 90.0 mm.
23. The second order reflection from (200) planes coincides with the first
order reflection from
A. (100) B. (200) C. (400) D. none of these
24. The interplanar spacing of the first reflecting plane (lowest q) in an FCC
crystal
A. a 3 B. a/ 3 C. a / 2 D. a
25. The first reflection from polonium powder (SC) occurs at Bragg angle of
28.7°. The fourth reflection is at Bragg angle
A. 57.4° B. 114.8° C. 73.8° D. none of these
26. If the first reflection from a BCC crystal has a Bragg angle q of 22.2°, the
second reflection will have a q of
A. 32.3° B. 25.9° C. 38.1° D. 44.4°
27. No reflection will be observed from a DC crystal (a = 3 Å) if the
wavelength of x-rays is greater than
A. 3.0 Å B. 3.25 Å C. 3.37 Å D. 3.46 Å
52 Source for Experimental Data/Suggestions for Further Reading
28. If the first reflection from a FCC crystal has a Bragg angle q of 21.5°, the
second reflection will have an angle q of
A. 18.5° B. 25° C. 31.2° D. 36.8°
29. The first three reflecting planes of silicon (DC) are
A. 111, 200, 220 B. 110, 200, 211
C. 111, 220, 311 D. 100, 110, 111
30. Using X-rays of 2.29 Å, the first two reflections have Bragg angles of
34.06° and 65.51°. The Bragg angle for the third reflection is
A. 68.1° B. 75.9° C. 89.9° D. reflection absent
31. The Miller indices of the fifth reflection in an FCC crystal is
A. 331 B. 222 C. 311 D. 400
Answers
1. A, B, C 2. D 3. D 4. B 5. C
6. B 7. D 8. D 9. B 10. B
11. A 12. B 13. A 14. B 15. C
16. D 17. B 18. B 19. A, C 20. B, C
21. D 22. D 23. C 24. B 25. C
26. A 27. D 28. B 29. C 30. D
31. B
4.9 The potential energy W for the formation of a bond between two univalent
ions is given by Eq. (4.4). A¢ = 1.13 ´ 1011 in appropriate SI units. The
equilibrium spacing r0 = 2.50 Å. Find the value of the constant B, given
m = 9.
Answer: 4.92 ´ 10–105 J m9.
4.10 The potential energy W of a system of two atoms varies as a function of
their distance of separation r as follows:
W = –A/r n + B/r m
Show that at equilibrium
(i) r = r0 = (mB/nA)1/(m – n),
(ii) the energy of attraction is m/n times the energy of repulsion, and
(ii) the bond energy W0 = A/r0n (m – n)/m.
4.11 Calculate the enthalpy of atomization of copper and tungsten from the
bond energy values given in Table 4.9.
Answer: 338.4 kJ mol–1; 849.2 kJ mol–1.
4.12 Explain why the bond lengths in Table 4.11 increase with increasing
atomic number, in spite of the increase in the bond energy.
4.13 Make a plot of the melting points and the boiling points of materials of
different bonding characteristics as a function of their bond energy.
4.14 Compare the values of the dipole moments given in Table 4.10 with the
electronegativity differences of the appropriate atoms and give reason for
any correlation you notice.
4.15 Explain why the increasing trend of melting and boiling points in
Table 4.12 shows a reversal after silicon, even though the bond energy
continues to increase.
4.16 The fraction of ionic character of a bond in a compound AB is given by
fionic = 1 – exp [–(XA – XB)2/4]
where XA and XB are the electronegativities of the elements A and B.
Calculate the fraction of ionic character of (i) GaAs, (ii) ZnS, and
(iii) AgCl.
Comment on the trend you observe.
Answer: (i) 0.04 (ii) 0.18 (iii) 0.26.
2. The order of increasing energy of orbitals in the sixth row of the Periodic
Table is
A. 6s4f 5d6p B. 6s6p4f 5d C. 6s6p6d6f D. 6s5f 5d6p
3. If an electron transition occurs across the energy gap in GaAs of 1.43 eV,
the radiation emitted or absorbed has a wavelength (Planck’s constant =
6.626 ´ 10–34 J s; velocity of light = 2.998 ´ 108 m s–1)
A. 86.7 Å B. 12400 Å C. 8670 Å D. 13890 Å
10 1
4. Nickel, which is to the left of Cu (3d 4s ) in the first transition series, has
an outer electron configuration
A. 3d94s1 B. 3d84s2 C. 3d114s1 D. 3d104s2
5. If there are six electrons in the d orbital of a transition metal, the number
of unpaired electrons are
A. 6 B. 5 C. 4 D. 0
–1
6. The electron affinity of He in kJ mol is
A. 369 B. –704 C. 86 D. 0
–1
7. Primary bonds have energy range in kJ mol
A. 1000–5000 B. 100–1000 C. 10–100 D. 1–10
8. If the Fe–Fe bond length is 2.48 Å, the radius of the iron atom is
A. 2.48 Å B. 1.75 Å C. 1.43 Å D. 1.24 Å
9. The tetrahedral bond angle of (sp3) bonds is
A. 90° B. 99° C. 104° D. 109.5°
–1
10. If copper has bond energy of 56 kJ mol of bonds, the enthalpy of
atomization of copper in the same units is about
A. 56 B. 112 C. 336 D. 672
11. Thermal expansion of materials arises from
A. strong bonds C. thermal vibrations
B. weak bonds D. asymmetry of potential energy curve
12. Hydrogen bonds are stronger than
A. van der Waals bonds C. ionic bonds
B. metallic bonds D. covalent bonds
13. If the radius of anion is ra and of cation is rc, the bond length is
A. (rc + ra) B. 3 (rc + ra) C. 3 /2 (rc + ra) D. ra – rc
80 Suggestions for Further Reading
Answers
1. C 2. A 3. C 4. B 5. C
6. D 7. B 8. D 9. D 10. C
11. D 12. A 13. A
M.F.C. Ladd, Structure and Bonding in Solid State Chemistry, Ellis Horwood,
Chichester, UK (1979).
L. Pauling, The Nature of the Chemical Bond, Cornell University Press, Ithaca
(1960).
H.H. Sisler, Electronic Structure, Properties and the Periodic Law, Reinhold
Publishing Corporation, New York (1963).
116 Problems/Multiple Choice Questions
5.35 Calculate the density and packing efficiency of the NaCl crystal.
Answer: 2230 kg m–3, 0.66.
5.36 List the space lattice, basis, number of ions of each type in the unit cell,
and lattice parameter-ionic radii relationships for the cubic ionic crystals
MgO and CsCl. The cation-to-anion ratios are 0.59 and 0.91, respectively.
5.37 Distinguish between thermoplastics and thermosets, using any three of
their characteristics.
5.38 On the basis of their structure, describe how elastomers are different from
the other long-chain polymers.
5.39 List the factors that promote noncrystallinity in long-chain polymers.
1. In the DC unit cell of silicon (a = 5.43 Å), the number of atoms per metre
along the body diagonal are
A. 8.5 ´ 109 m–l B. 2.1 ´ 109 m–1
C. 2.6 ´ 10 m
9 –1
D. 1.84 ´ 109 m–1
2. The average distance between atoms along the body diagonal of the DC
crystal is
A. a 3/4 B. a 3/8 C. a 3/2 D. a 3
3. If the lattice parameter of Si = 5.43 Å and the mass of Si atom is 28.08 ´
1.66 ´ 10–27 kg, the density of silicon in kg m–3 is
A. 2330 B. 1115 C. 3445 D. 1673
4. The close packed direction in Ge crystal is
A. [100] B. [110] C. [111] D. none of these
5. The lattice parameter of GaAs (radius of Ga = 1.22 Å, As = 1.25 Å) is
A. 5.635 Å B. 5.704 Å C. 5.774 Å D. 4.94 Å
6. In cubic ZnS (II-VI compound), if the radii of Zn and S atoms are 0.83 Å
and 1.74 Å, the lattice parameter of cubic ZnS is
A. 11.87 Å B. 5.94 Å C. 5.14 Å D. 2.97 Å
7. The number of atoms along the body diagonal of the diamond cubic unit
cell is
A. 1 B. 2 C. 3 D. 4
8. The close packed directions that lie on a (111) plane of an FCC crystal are
A. [101], [110], [0 1 1] B. [11 1], [1 11]
C. [100], [0 10], [00 1] D. [10 1], [1 10], [011]
Multiple Choice Questions 117
21. The density of the CsCl crystal with ionic radii of Cs+ = 1.65 Å and Cl–
= 1.81 Å is (at.wt. Cs = 132.9, Cl = 35.45; 1 amu = 1.66 ´ 10–27 kg)
A. 4383 kg m–3 B. 3373 kg m–3 C. 2386 kg m–3 D. 6746 kg m–3
22. The fraction of octahedral voids filled by Al3+ ions in Al2O3
(rAl3+/rO2– = 0.43) is
A. 0.43 B. 0.287 C. 0.667 D. 1
23. If the lattice parameter of CsCl is 3.995 Å, the bond length (between
bonding species) is
A. 3.46 Å B. 6.92 Å C. 1.73 Å D. 5.65 Å
24. The packing efficiency of a NaCl crystal (radius of Na+ = 0.98 Å, Cl– =
1.81 Å) is
A. 0.52 B. 0.66 C. 0.68 D. 0.74
25. In ruby, Cr3+ ions substitute for
A. Al3+ ions B. Fe3+ ions C. Mg2+ ions D. O2– ions
26. In CaF2 with the eight-fold cubic coordination, the fraction of voids at the
body centre occupied by Ca2+ ions is
A. 1 B. 0.5 C. 0.25 D. 0
27. The length of an uncoiled polyethylene chain with 500 mers is (C–C bond
length = 1.54 Å)
A. 500 Å B. 770 Å C. 1540 Å D. 1258 Å
28. Apart from three H atoms, the fourth side group in the monomer of
polypropylene is
A. Cl B. CH3 C. C6H5 D. COOCH3
29. The side groups in polyvinyl chloride are
A. H, H, H, H B. H, H, H, Cl C. H, H, CH3, Cl D. H, Cl, Cl, Cl
30. The weight of sulphur in kg required to achieve 5% cross-linking of 68 kg
of polyisoprene is
A. 1.6 kg B. 3.2 kg C. 16 kg D. 32 kg
31. The factors that promote noncrystallinity in polymers are
A. large random side groups B. branching
C. addition of plasticizers D. copolymerization
32. The degree of polymerization in polyethylene is 50,000. The average
molecular weight in amu is
A. 700,000 B. 1,300,000 C. 1,400,000 D. none of these
33. In the PTFE (teflon) monomer, the four side groups are
A. F, F, F, F B. H, H, H, H C. H, H, H, Cl D. H, H, H, CH3
34. The weight in amu of a polyethylene chain with 1000 mers is
A. 28,000 B. 280,000 C. 62,000 D. 42,000
Sources for Experimental Data/Suggestions for Further Reading 119
35. The minimum number of double bonds required in the monomer for cross-
linking is
A. 0 B. 1 C. 2 D. 3
36. The bulkiest side group in the monomer is in
A. teflon B. PVC C. PTFE D. polystyrene
37. The chemical formula of the isoprene molecule is
A. C4H5CH3 B. C3H4CH3Cl C. C4H3Cl D. C2H3CH3
Answers
1. B 2. C 3. A 4. D 5. B
6. B 7. B 8. A, D 9. B 10. A, B, C
11. C 12. B 13. D 14. C 15. C
16. C 17. B 18. B, D 19. D 20. B
21. A 22. C 23. A 24. B 25. A
26. B 27. D 28. B 29. B 30. A
31. A, B, C, D 32. C 33. A 34. A 35. C
36. D 37. A
Answers
1. B 2. B 3. A 4. A, D 5. A
6. A 7. A 8. A 9. D 10. C
11. A 12. B 13. C, D 14. B 15. C
16. C
J.P. Hirth and J. Lothe, Theory of Dislocations, McGraw-Hill, New York (1984).
A. Kelly, G.W. Groves and P. Kidd, Crystallography and Crystal Defects, John
Wiley, Chichester, UK (2000).
Problems/Multiple Choice Questions 175
3. The degree of freedom when ice, water and water vapour co-exist in
equilibrium is
A. 1 B. triple pt C. 0 D. –1
4. The degrees of freedom, when FCC iron and BCC iron co-exist in
equilibrium, are
A. 2 B. 1 C. 0 D. –1
5. The phase boundary between alpha and (alpha + beta) regions is called
A. liquidus B. solidus C. solvus D. none of these
6. The reaction that yields two solid phases on cooling a single solid phase is
called
A. eutectoid B. peritectoid C. eutectic D. congruent
7. If one solid phase splits into two solid phases on heating, the reaction is
A. eutectic B. peritectic C. eutectoid D. peritectoid
8. The reaction that, on heating one solid phase, yields another solid phase
plus one liquid phase is called
A. eutectic B. eutectoid C. peritectic D. peritectoid
9. If alpha of 82% B and liquid of 57% B are in equilibrium in an alloy of
73% B, the fraction of liquid is
A. 0.36 B. 0.64 C. 36% B D. 0
10. If the fraction of liquid with 57% B, which is in equilibrium with solid of
82% B, is 0.7, the overall composition is
A. 0.3 B. 74.5% B C. 64.5% B D. 25% B
11. In the eutectic phase diagram of Ag–Cu system, the solubility limit at
500°C of copper is 3% in the Ag-rich phase and of Ag is 2% in the
Cu-rich phase. In sterling silver (92.5% Ag –7.5% Cu), the per cent of
copper in the Ag-rich phase at 500°C is
A. 95.26 B. 4.74 C. 3 D. 98
12. The eutectic mixture in a Pb–Sn solder alloy should be 90%. At the
eutectic temperature, alpha of 19% Sn, liquid of 62% Sn and beta of 97%
Sn are in equilibrium. The possible compositions of the solder alloy are
A. 57.7% Sn B. 61% Sn C. 65.5% Sn D. 66.3% Sn
13. The fraction of pearlite in a 0.55% C steel is
A. 0.55 B. 0.31 C. 0.69 D. 0
14. At 30°C, hot chocolate (liquid) with 35% chocolate and 65% vanilla
transforms to chocolate ripple (eutectic mixture of vanilla containing 10%
chocolate and chocolate containing 5% vanilla). Just below 30°C, the
fraction of chocolate ripple in a composition with 45% chocolate is
A. 0.17 B. 0.83 C. 0.41 D. 0.59
Sources for Experimental Data/Suggestions for Further Reading 177
15. Zone refining will be more efficient if the ratio of impurity in the solid to
that in the liquid is
A. 0.01 B. 0.1 C. 0.4 D. ~1.0
Answers
1. D 2. B 3. C 4. B 5. C
6. A 7. D 8. C 9. A 10. C
11. C 12. A, C 13. C 14. B 15. A
W.D. Kingery, H.K. Bowen and D.R. Uhlmann, Introduction to Ceramics, Wiley,
New York (1976), Chap. 7.
A. Prince, Alloy Phase Equilibria, Elsevier, Amsterdam (1966).
F.N. Rhines, Phase Diagrams in Metallurgy, McGraw-Hill, New York (1956).
Multiple Choice Questions 199
11. If the enthalpy of motion of a vacancy is 100 kJ mol–1, the time that a
vacancy takes to jump to an adjacent site at 25°C is about
A. 3 ´ 1017 s B. 2 ´ 1026 s C. 1013 s D. 3 ´ 104 s
12. The units of the ratio s /D (= ne2z/kT) are
A. A2 m–3 J–1 B. C2 m–3 J–1 C. C2 m–3 J D. V2 A–2 m–3 J
Answers
1. C 2. A, C 3. C 4. B 5. D
6. D 7. D 8. D 9. A 10. C
11. D 12. B
J. Crank and G.S. Park, Diffusion in Polymers, Academic Press, New York
(1968).
W.D. Kingery, H.K. Bowen and D.R. Uhlmann, Introduction to Ceramics, Wiley,
New York (1976), Chap. 6.
P.G. Shewmon, Diffusion in Solids, McGraw-Hill, New York (1963).
Multiple Choice Questions 235
9.28 At any instant of time, the grain growth, i.e., the rate of increase of the
grain radius with time, dr/dt, is proportional to the grain boundary energy
stored per unit volume of the material. Show that the radius of spherical
grains increases as the square root of time.
Answers
1. B 2. C 3. C 4. D 5. D
6. D 7. A 8. B, C, D 9. A, B, C 10. A
11. B, D 12. C 13. B 14. A 15. D
16. C 17. C 18. B 19. A, C, D 20. C
W.D. Kingery, H.K. Bowen and D.R. Uhlmann, Introduction to Ceramics, Wiley,
New York (1976), Chaps. 8–10.
V. Raghavan, Solid State Phase Transformations, Prentice-Hall of India, New
Delhi (1987).
Problems/Multiple Choice Questions 257
Answers
1. A, C 2. A 3. D 4. C 5. C
6. B 7. B, C 8. A 9. A 10. C
11. B 12. D
K.A. Gschneidner Jr., in Solid State Physics (1964), Vol. 16, p. 275 on Physical
Properties and Interrelationships of Metallic and Semimetallic Elements.
294 Problems/Multiple Choice Questions
11.22 Compute the mean grain diameters in mm, corresponding to ASTM grain
size numbers (i) 3, (ii) 0, and (iii) –2.5.
Answer: 0.125 mm, 0.35 mm, and 0.84 mm.
11.23 A grain size of ASTM 7 in a mild steel is refined to ASTM 14 by the
addition of microalloying elements. Estimate the increase in the yield
strength of the steel.
Answer: 300 MN m–2.
11.24 Two samples of an Fe-3%Si alloy have grain sizes of ASTM 1 and 8
respectively. They have yield strengths of 118 and 207 MN m–2.
Calculate the yield strength of a single crystal of this alloy.
Answer: 8l MN m–2.
11.25 Estimate the yield strength of a cold-worked microalloyed steel from the
following data:
Peierls–Nabarro (tensile) stress for Fe : 35 MN m–2
Solid solution strengthening by Mn and Si : 135 MN m–2
Dislocation density due to cold working : 1014 m–2
ASTM grain size number : 13
Assume that the constant A in the work hardening equation is 10 N m–1.
Answer: 630 MN m–2.
11.26 Describe briefly the main strengthening methods against plastic yield at
low temperatures.
11.27 Reexamine critically the above strengthening methods against plastic
yield for temperatures above 0.4Tm.
11.28 Discuss the role of (i) grain boundaries and (ii) precipitate particles, in
strengthening crystalline materials against yield at low as well as high
temperatures of deformation.
13. The yield stress of a copper crystal is 100 and 10 MN m–2, when cold
worked to a dislocation density of 3 ´ 1014 and 2 ´ 1012 m–2, respectively.
The yield stress of the softest crystal is
A. 0 MN m–2 B. 2 MN m–2 C. 10 MN m–2 D. 3.33 MN m–2
14. If ASTM grain size number 7 corresponds to grain diameter of 0.03 mm,
ASTM 4 corresponds to
A. 0.24 mm B. 0.085 mm C. 0.011 mm D. 0.004 mm
15. A grain size measured wrongly at a magnification of 300 ´ gave an ASTM
number of 2. The correct grain size number should be
A. –1 B. 5.2 C. 6.0 D. 5.0
16. The mean grain diameter corresponding to ASTM number = – 0.5 is
A. 5 mm B. 0.05 mm C. 0.43 mm D. 0.30 mm
17. The ASTM grain size number of a material which has 28 grains per sq.in.
at a magnification 75 ´ is about
A. 14 B. 7 C. 5 D. 4
18. A mild steel (k = 0.7 MN m–3/2) of 0.03 mm grain diameter is grain
refined to 0.003 mm. The increase in yield strength (MN m–2) will be
about
A. 275 B. –275 C. –0.00275 D. 8.1
19. The yield stresses of an Fe-4%Si alloy at grain sizes of 0.015 and
0.045 mm are 214 and 147 MN m–2. The yield stress of a single crystal is
A. 55.5 MN m–2 B. 120 MN m–2 C. 80 MN m–2 D. 360 MN m–2
20. The yield stresses of both Au and Ag single crystals are 0.7 MPa. The
yield stress of a 50 : 50 solid solution is
A. 0.7 MPa B. > 0.7 MPa C. < 0.7 MPa D. 0
21. The radii of copper, zinc and tin are 1.28, 1.31 and 1.51 Å respectively. As
compared to zinc, tin in copper will produce a strengthening effect that is
A. large B. small C. very small D. same
22. When the inter-precipitate spacing increases from 200 to 2000 Å, the ratio
of the new yield strength to the initial strength is
A. 10 B. 1 C. 0.1 D. none of these
23. The methods to increase the yield strength of a crystalline material are
A. grain refinement B. annealing
C. solute additions D. precipitation hardening
24. The most desirable method of increasing the yield strength of mild steel is
A. grain refinement B. cold working
C. solute additions D. precipitation hardening
Sources for Experimental Data/Suggestions for Further Reading 297
Answers
1. A 2. B, C 3. C 4. C 5. D
6. D 7. C 8. D 9. B 10. A
11. A 12. C 13. B 14. B 15. B
16. C 17. C 18. A 19. A 20. B
21. A 22. C 23. A, C, D 24. A 25. D
26. A, C 27. B
ASM International, Metals Handbook, 10th ed., Vol. 1, Irons and Steels and
High Performance Alloys: Specialty Steels and Heat Resistant Alloys,
pp. 755–1003, Materials Park, Ohio (1990).
A. Kelly and R.B. Nicholson, Strengthening Methods in Crystals, Elsevier,
Amsterdam (1971).
12.11 A heat treated steel chisel and a glass window pane are both brittle.
Explain why the chisel is strong and the window pane is weak.
12.12 Suggest one of the following alloys for use as a container for liquid
oxygen in a rocket, giving your reasons for the choice: mild steel, copper
and austenitic stainless steel.
12.13 When a sodium silicate glass is immersed in a lithium nitrate bath at
260°C for a few minutes, cracks develop on the surface. Why?
12.14 A sample of borosilicate glass contains two cracks: a surface crack of
1 mm deep and an inner crack of 1.8 mm long. Both the cracks
are normal to the tensile axis. Determine which one will propagate
first on increasing the applied load and at what stress? Y = 65 GN m–2;
g = 0.5 J m–2.
Answer: Surface crack at 144 MN m–2.
12.15 A sheet of glass, with Y = 70 GN m–2 and g = 0.5 J m–2, has an internal
crack of length equal to 2 mm. A surface crack of 0.8 mm depth is
introduced by scratching the surface with a sharp tool. Adsorption at the
surface lowers the surface energy by 50%. Determine which crack will
propagate first, on increasing the applied stress and at what value of the
stress?
Answer: Surface crack at 118 MN m –2.
12.16 Estimate the fracture strength of a sodium silicate glass with Y = 70 GN
m–2 and g = 0.5 J m–2. A number of cracks are present both inside and on
the surface of the glass, varying in size from 1 to 5 mm. How will the
fracture strength change, if the glass is dipped in (i) HF solution, and
(ii) LiNO3 solution?
Answer: 67 MN m –2.
Answers
1. B 2. C 3. A 4. D 5. B
6. B 7. B 8. C 9. A, B, C 10. D
13.5 What is the potential difference that is observed, when a standard zinc
electrode is connected to the calomel reference electrode whose potential
is + 0.334 V?
Answer: 1.094 V.
13.6 Calculate the ampere-hour required to plate out one mole of copper from
a copper sulphate solution.
Answer: 53.61 A hr.
13.7 Calculate the cupric ion concentration in the elecrolyte that is required to
make the potential of copper to become equal to that of the standard zinc
electrode. Is this potential likely to be realized in practice? Explain.
Answer: 1.0 ´ 10–37.
13.8 1 mm thick layer of nickel is to be plated on a steel article. What is the
current density required to do this in one hour?
Answer: 8130 A m–2.
13.9 Why is tin preferred to zinc on a steel food can? Why is enamelling
preferred to paint on a steel refrigerator body?
13.10 Show how rust, Fe(OH)3, can form in a galvanic cell, where iron is the
anode and the cathode reaction is as given in Eq. (13.5).
13.11 Which of the following coatings is expected to protect iron even if the
coating has cracks: Polyethylene, enamel, Zn, Ni, Sn and Pb? Give a
reason for your answer.
Answer: Zn.
1. For a protective oxide layer to form, the ratio of the volume of oxide
formed to that of metal consumed should be
A. < 1 B. 1 C. > 1 D. 1
2. The keys to good oxidation resistance of an oxide film are
A. low electrical conductivity B. low electrical resistivity
C. continuous oxide film D. porous oxide film
3. In parabolic rate of oxidation, the oxide thickness is proportional to
A. t1/2 B. t C. t2 D. none of these
4. Tick the elements added to iron to improve its oxidation resistance
A. zinc B. chromium C. magnesium D. aluminium
5. If the activation energy for oxidation is 100 kJ/mol, the ratio of oxidation
rates at 800 and 500°C is
A. 8270 B. 78 C. 1.0 D. 0.031
Sources for Experimental Data/Suggestions for Further Reading 331
Answers
1. C 2. A, C 3. A 4. B, D 5. B
6. A 7. A 8. C 9. A 10. A
S. Lamb (Ed.) Practical Handbook of Stainless Steels and Nickel Alloys, ASM
International, Materials Park, Ohio (1999).
14.16 Explain why aluminium used in long distance transmission lines cannot
be strengthened by solid solution.
Answers
1. A 2. A 3. C 4. C 5. B
6. C 7. B 8. C 9. A 10. C
11. D 12. A, B 13. C 14. C 15. B
16. A 17. C 18. C 19. C 20. C
21. D 22. D 23. B, C, D 24. C 25. A, B, C
26. D 27. A, B 28. C 29. A, B, C 30. A, C
31. A 32. A 33. B 34. A, B, C
C. Kittel, Introduction to Solid State Physics, Wiley, New York (1976), Chaps. 6
and 12.
L.E. Murr, A.W. Hare and N.G. Eror, Introducing the Metal Matrix High
Temperature Superconductor, in Advanced Materials and Processes, ASM
International, Materials Park, Ohio (1987), Vol. 145(10), pp. 36–44.
Problems/Multiple Choice Questions 387
6. The fraction of electrons excited across the energy gap in Ge (Eg = 0.7 eV)
at room temperature is
A. 0 B. l.7 ´ 10–12 C. 2 ´ 10–12 D. 1.3 ´ 10–6
7. During an electron transition across the energy gap in Si,
A. the momentum of the electron changes
B. the direction of motion of the electron changes
C. the potential energy of the electron changes
D. the kinetic energy of the electron remains constant
8. The energy gap in divalent metals is
A. very small B. fairly small C. zero D. large
9. If the electron positions corresponding to the standing wave solutions in
Ge (energy gap = 0.7 eV) differ by 1.22 Å, the field gradient in V m–1
required to promote an electron to the conduction band is
A. 0.85 ´ 1010 B. 0.57 ´ 1010 C. 106 D. 0.7
10. Pure silicon at 0 K is an
A. intrinsic semiconductor B. extrinsic semiconductor
C. metal D. insulator
11. The temperature at which the resistivity of pure diamond will equal that of
pure Si at room temperature is
A. above m.p. of diamond B. 3000 K
C. 300 K D. can’t be estimated without data
12. Ignoring variation in mobilities, the temperature at which pure Si will have
the same conductivity as pure Ge at 300 K is
A. 190 K B. 300 K C. 470 K D. 1470 K
13. The resistivity of pure silicon at 0°C is 3000 ohm m. The intrinsic carrier
density per cubic metre is ( me = 0.14 and m h = 0.05 m2 V–1 s–1)
A. 1.095 ´ 1016 B. 2.19 ´ 1016 C. 1018 D. zero
14. In an extrinsic semiconductor, in the region where mobility variation with
temperature is evident, the slope of log(conductivity) vs. l/T plot is
A. positive B. negative C. 0 D. infinity
15. The two most common doping elements in Si are
A. P B. B C. Sb D. Bi
16. The majority charge carriers in p-type Ge are
A. free electrons B. ions
C. holes D. conduction electrons
17. The temperature at which 50% of holes become available for conduction in
B-doped Si (ionization energy = 0.045 eV) is
A. 52°C B. 104°C C. 377°C D. 480°C
18. If the drift velocity of holes under a field gradient of 100 V m–1 is
5 m s–1, their mobility (in the same SI units) is
A. 0.05 B. 0.5 C. 50 D.500
Multiple Choice Questions 389
Answers
1. D 2. D 3. D 4. A 5. A
6. D 7. A, B, C, D 8. C 9. B 10. D
11. D 12. C 13. A 14. A 15. A, B
16. C 17. D 18. A 19. C 20. B, C
21. C 22. B 23. A 24. A 25. C
26. A 27. C, D 28. B, C 29. D 30. C
31. A 32. A 33. C 34. A 35. A
36. C 37. B 38. C 39. A, C, D 40. A
41. B 42. D 43. A, B, C 44. B, C 45. B
46. A 47. A 48. D
Multiple Choice Questions 409
Answers
1. C, D 2. D 3. B 4. B 5. A
6. B 7. B 8. D 9. A 10. C
11. A, B, C, D 12. A 13. A 14. D 15. A
16. B 17. A 18. B 19. C 20. C
21. A
424 Problems
PROBLEMS
17.1 The electric field strength can be expressed as V m–1 or as N C–1. Express
these in base SI units and show that they are equivalent.
17.2 Derive the units of ae from that of E and the dipole moment.
17.3 Find the capacitance of a layer of Al2O3 that is 0.5 mm thick and
2000 mm2 of surface area. er = 8.
Answer: 2.83 ´ 10–7 F.
17.4 The electronic polarizability of helium is 0.18 ´ 10–40 F m2. Calculate its
relative dielectric constant at 0°C and 1 atm pressure.
Answer: 1.000 055.
17.5 Estimate the shift of the electron cloud with respect to the nucleus in an
argon atom, when a field of 105 V m–1 is applied.
Answer: 5 ´ 10–18 m.
17.6 The dielectric constant of polyethylene is independent of temperature,
while that of polyvinylchloride is not. Explain this difference in
behaviour on the basis of their monomer structures.
17.7 When ice melts into water, the dielectric constant increases, in contrast to
the decrease observed during the melting of HCl. Explain why this is so.
17.8 What is the variation expected in the loss factor in a sodium silicate
glass, when some of the Na+ ions are replaced by Rb+ ions? Explain.
17.9 Compare the hysteresis loops in Figs. 16.4 and 17.6. Explain why there is
a constant saturation induction Bs in Fig. 16.4, and no saturation value of
polarization in Fig. 17.6.
Answers
1. A 2. C 3. B 4. C 5. B
6. A 7. D 8. B 9. A 10. C
11. D 12. C 13. D