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Hull 1964
Hull 1964
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BY D. HULLAND F. NOBLE
Dept. of Metallurgy, The University, Liverpool, 3
Received 15th June, 1964
Three indirect methods of determining the variation of dislocation velocity with stress are de-
scribed and their limitations discussed. Experiments on single crystals of silicon iron have shown
that the three methods give comparable results. The variation of the parameter rn, in the empirical
relation II = (./TO)" between velocity and stress, has been measured as a function of strain using a
stress relaxation method and the results considered in relation to.observations on the macroscopic
deformation processes in single crystals. Additional experimental observations using the relaxation
method are presented for polycrystalline silicon iron, pure iron and tantalum, and for tantalum
single crystals.
Gilman 1 found that the rapid variation of dislocation velocity with applied stress
in lithium fluoride could be described by
v = vo exp (-A/z), (1)
where vo is the elastic shear wave velocity of the material and z the applied stress.
Stein and Low 2 also found that their velocity data for dislocations in iron+3& <;
silicon could be expressed in this way, though an extrapolation to 112 = 0 did not
give the shear wave velocity for this material. Over the lower range of dislocation
velocities the relation
D = (.Cl.to)", (2)
where 70 is the resolved shear'stress required to produce a dislocation velocity of
1 cm sec-1 and m is a constant characteristic of the temperature and material, has
been found to represent adequately the lithium fluoride and silicon iron results.
Schadler 3 has confirmed this relationship for tungsten,
Both relations (1) and (2) are purely empirical and, in particular, refer to results
at a particular temperature. Johnston and GiIman 4 found that the temperature
dependence could be represented by
v = (z/zo)mexp (-E/kT), (3)
where E is the activation energy associated with dislocation movement. This relation
was found to be applicable to silicon iron only over a small range of stress and
temperature.
In attempts 6 to study dislocation mobility by indirect experiments, the velocity-
59
stress relationship in eqn. (2) has been assumed to apply and the value of the exponent
m obtained in such experiments compared with the value obtained by direct observa-
tion. The basis of the indirect experiments is the relation
E = bpv (4)
where 4 is the plastic strain rate and p is the density of moving dislocations. Assuming
p is constant at constant strain and substituting from eqn. (2),
4 = Kz", (5)
25 1
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D . H U L L A N D F . NOBLE 253
can be applied to the specimen in a dead loading machine. Changes in strain rate
are large (fig. 2) even for small load increments. Machine transients are not necessarily
eliminated in this test but can be completely eliminated in the third type of test
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(fig. 3). The value of m is obtained from the full relaxation curve, and good agree-
ment is obtained with eqn. (12), as demonstrated in fig. 4. Since it was assumed in
the derivation of eqn. (12) that the dislocation density remained constant this type of
experiment provides a direct check on this postulate.
elongation, %
FIG.1.-Change in flow stress associated with change in strain rate for a single crystal of silicon
iron at 293°K.
In table 1 the values of rn for iron +3$ % silicon single crystals (orientation as
in fig. 1) determined using the three tests are listed. As shown later, m is independent
of strain during the Luders strain but changes during work hardening and depends
on strain ; the work-hardening values refer, therefore, to a given strain ( 0.03). N
The results are in fairly good agreement and give confidence that each method gives a
true value of pn for the specimen. It seems most unlikely that a substantial change
in the mobile dislocation density, as postulated by Guard,s can occur to the same
-
Test region region, strain 4 - 0 3
(1) strain rate change 54 75
(2) load increments 53 - 84
(3) stress relaxation 58 N 77
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(b)
W o r k Hardening Region
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Luders . Region
0
strain time
FIG.3.-Stress relaxation curve for a single crystal of silicon iron at 293°K
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D . H U L L A N D F . NOBLE 255
extent in the three types of test to give similar values of m. If one accepts that the
values of rn measured are due solely to the movement of dislocations then these values
may be used as a basis for assessing the relevancy of direct observations of dislocation
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orientations and testing temperatures and it was possible to follow the formation
and growth of slip lines during deformation on the polished surfaces of the crystals
using an optical microscope attached to the tensile machine. Plastic deformation is
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initiated usually at both specimen grips in the form of discrete, coarse, slip lines.
Yielding occurs by the spread of the deformation in four ways : (i) the slip lines grow
in length across the specimen; (ii) further slip occurs within the slipped volume
producing larger steps on the surface; (iii) the slip lines broaden, often into wide
bands; (iv) new slip lines are nucleated further along the specimen and between
existing slip lines.
E
i
w
-
4
In this way a stable slip band configuration, as shown in fig. 5, is established and
this propagates down the gauge length as a Luders band. No discontinuity in this
process is observed during the yield drop (if one is present). Macroscopic work
hardening occurs when the Luders region completely covers the specimen and there
are no more deformation-free regons. Since an important contribution to the
Luders strain is the movement of slip lines into undeformed parts of the crystal
some direct correlation is expected between directly and indirectly determined values
of m.
In fig. 6 a typical set of results from stress relaxation tests at different strains has
been plotted. rn is independent of strain during the Luders strain and then increases
sharply at the onset of work hardening. There is a slow increase of m during work
hardening. The variation of rn with strain was found to be almost independent of
orientation. Two specific orientations were studied in more detail. These were
chosen such that, at 293"K, slip was restricted to (a) two { 1 lo} (1 11) systems, i.e., the
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FIG. 5.. -Distribution of slip bands at the Luders front in a single crystal of silicon iron ( x 100).
[Toface page 256.
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table 2 demonstrates that there is only a small, and probably insignificant, difference
between m in these two extreme cases. This agrees with Erickson's etch-pit observa-
tions 9 that the stress dependence of the velocity of dislocations moving in (1 12)
planes is the same as for dislocations moving in (110) planes, as measured by Stein
and Low.2 Table 2 also gives values of m determined by stress relaxation at 77°K
and shows that in this material there is only a small variation of m with temperature
cf. Stein and Low 2, which is only significant in the Luders strain region.
(a) Crystal oriented for (110) slip tested at 293°K; Luders strain = 0-038
strain true tensile stress m
kg mm-2
0.005 323 64
0-014 32.3 64
0.027 31.9 61
0.052 33.1 76
0.083 35.5 79
0.133 38.0 80
0.197 40.5 81
0.236 42.0 85
(b) Crystal oriented for (112) slip tested at 293°K; luders strain = 0.004
strain true tensile stress m
kg mm-2
0.0002 31-4 59
0.0017 31-4 62
0.016 326 68
0.041 346 71
0.088 37-1 82
0.260 46.0 86
(c) Crystals oriented for (1 10) slip tested at 77°K ; Luders strain = 0-054
strain true tensile stress m
kg mm-a
0405 70 76
0.025 69.5 73
0.044 69.5 74
0.085 76.2 81
0.121 80.5 82
0.176 87.0 82
measured slip lines in a given specimen. It was found that the slip lines did not move
at a uniform velocity and for a given time of pulse the velocity of the individual slip
lines varied over a wide range. In spite of the limited reproducibility of results nz,
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determined by this method, was usually between 40 and 50, and a line corresponding
to rn = 40 is marked in fig. 7.
log velocity
FIG.7.-Variation of the velocity of the tips ofslip bands as a function of stress for a single crystal
of silicon iron tested at 293°K.
For comparison and information, the results of stress relaxation tests on poly-
crystalline silicon iron, pure iron (0.004 % C), and tantalum, and single crystals of
tantalum are listed in table 3. The polycrystalline silicon iron gave comparable,
though slightly higher, values of m to those in single crystals. The polycrystalline
iron and tantalum showed exceptionally marked increases of m at the onset of work
(b) VARIATION
OF m WITH STRAIN FOR SINGLE CRYSTALS OF TANTALUM
temp. OK LGde,s region work-hardening
region
293 11 13-23
77 87 87
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D . H U L L A N D F. NOBLE 259
hardening and fig. 8 demonstrates this particularly well. In the tantalum single
crystals, m was appreciably lower in the Luders-strain region than in the poly-
crystalline material, although this might be due to compositional changes. The
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orientation of the crystal was such that the Luders strain was short. The crystals
deformed in a similar way to the silicon-iron single crystals. In contrast to the silicon
iron there was a marked dependence of rn on temperature.
.4 1-0 2.0
log time
FIG.8 . 4 tress relaxation curves of polycrystallinepure iron at 293°K showing pronounced changein
slope at the end of Luders strain, (log u is replaced by A u in this example, see reference 8).
DISCUSSION
All the results show a definite discontinuity in the indirectly determined values of
m obtained in the Luders and work-hardening regions. In silicon-iron single crystals
this discontinuity is slight but reproducible. The values of rn obtained in the Luders
region are constant and lower than values obtained in the work-hardening region.
In the work-hardening region, m becomes greater with increasing strain when the
applied stress is used in calculating rn and hence extrapolation in the work-hardening
region as discussed previously may be justified. However, in crystals which show a
Luders region, extrapolation to zero strain can only be performed by ignoring the
constant values obtained in this region. The justification for such a procedure is
far from clear.
Good agreement with the results of direct observation experiments is expected
only when exactly the same process is being studied in each case. Since the direct
method involves the propagation of a slip line into undeformed material this process
must be responsiblefor the whole of the observed strain rate in the indirect experiments
if agreement is to be achieved. Undoubtedly, this process is contributing to the
Luders-strain rate in the deformation of a single crystal but the contribution to the
strain rate by the propagation of a limited number of slip lines is likely to be small in
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260 E F F E C T O F STRESS ON D i S L O C A T l O N V E L O C l T Y
proportion to the strain rate contribution due to continuing deformation in the existing
slip lines. The process being studied in the indirect test in the Liiders region is
therefore the mobility of dislocations in an already deformed region with a small
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contribution from the dislocations at the tips of the slip lines moving into undeformed
material. In the steady state-region of Liiders propagation a constant value of m
should be obtained since there will be a fixed contribution to the plastic strain rate by
the various mechanisms. When work hardening begins, the small contribution
from the slip-line tips vanishes and a discontinuity in values of m occurs at this point.
Because the contribution from the slip-line tips is small similar values of m should be
obtained in both Liiders and work-hardening regions because essentially the same
process is being studied in each case. It is not clear why values of m should be
higher even at the yield point for dislocations moving within slip bands though the
reason is probably due to the velocity distribution which exists within the bands and
the complex stress field through which the dislocation moves.
Evaluation of the values of m obtained in the work-hardening region assuming the
effective stress on the dislocations was constant at the value at the end of the Luders
region did not give a constant m but the values obtained were more nearly constant
than if the applied stress were used.
The values of m obtained in the tests on polycrystalline silicon iron follow much
the same pattern as those for the single crystals but the values in general are slightly
higher. As with single crystals, a slight but reproducible discontinuity in values of m
between Luders and work-hardening regions is observed. Constancy of m in the
Luders region is found as would be expected. The results may be explained by
analogy with the single crystal results, namely, that in the Luders region by far the
greater contribution to the strain rate is due to the movement of dislocations in already
yielded grains behind the Luders front. The reason for the slightly lower values
obtained in the Luders region is the small but measurable contribution of the dis-
location movement in the grains in the process of YieldingattheLiidersfront. Such an
explanation implies a fairly wide Luders-strain profile and a diffuse band front in
silicon iron. At low enough strains, therefore, the band may not be fully developed
and the contribution from the yielding grains in the Liiders front will be correspond-
ingly enhanced. The lower values of m which were obtained close to the yield point
may be the result of such a situation.
Unfortunately, no directly observed values are available for pure iron or tantalum
so the results of relaxation experiments can only be compared with the corresponding
tests on silicon iron. For the polycrystalline case the change in values of m obtained
in Luders and work-hardening regions is very large-about three times. If we
accept the above reasoning on Luders-band profiles, then these results suggest that
in polycrystalline pure iron and tantalum the Liiders profile is extremely sharp and
that the yielding grains in the front are the only ones contributing to the deformation
rate.
As with silicon iron, the values of rn obtained in the Liiders region for polycrystal-
line tantalum are somewhat higher than for the single crystal results. This dis-
crepancy is presumably due to the effect of really measuring a weighted average of m
in the polycrystalline case as discussed by Li.10
The activation volume associated with any particular value of m can be calculated
from eqn. (9). The results show a considerable discontinuous change in u* between
the Luders and work-hardening regions, particularly in polycrystalline pure iron and
tantalum. These results contradict those of Conrad 7 who found that in pure iron
v* was independent of the deformation process occurring. However, in silicon iron
the indirectly determined values of m in the Liiders region are closer to those determined
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We are grateful to many colleagues for helpful discussion. One of us (F. N.)
acknowledgesthe generous financial assistance provided by a Leverhulme Fellowship.
1Ghan, in
Fracture, Wiley, 1959.
2 Stein and Low, J. Appl. Physics, 1960,31, 362.
3 Schadler, Acta. Met., to be
published.
4 Johnston and Gilman, J. Appl. Physics, 1959,30, 129.
5 Guard, Acta Met., 1961, 9, 163.
6 Johnston and Stein, Acta Met., 1963, 11, 317.
7 Conrad, J. Iron Steel Inst., 1961,198, 364.
* Noble and Hull, Acta Met., to be published.
9 Erickson, J. Appl. Physics, 1962,33,2499.
10 Li, U.S. Steel Report No. 1129, 1963.