Comments on the determination of vacancy parameters in calorimetric studies

Comments on the determination of vacancy parameters in calorimetric studies

Scripta METALLURGICA V o l . 7, pp. 4 2 7 - 4 3 0 , 1973 P r i n t e d in the U n i t e d S t a t e s COMMENTS ON THE DETERMINATION * ** and Pre...

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Scripta

METALLURGICA

V o l . 7, pp. 4 2 7 - 4 3 0 , 1973 P r i n t e d in the U n i t e d S t a t e s

COMMENTS ON THE DETERMINATION

* **

and

Press,

Inc,

OF VACANCY PARAMETERS

IN C A L O R I M E T R I C

G. M O Y A *

Pergamon

STUDIES

A. COUJOU * *

Laboratoire de Mbtallurgie - Universit~ de Provence, Centre de Saint J@rome - 13013 Marseille ,ffFrance) Laboratoire de Physique Electronique, Etude du m~tal - Universit~ Paul Sabatier- 31004 Toulouse (France)

(Received

February

8,

1973)

To date, few studies on quenched-in vacancies in metals are based upon calorimetric technique. However, among the various properties used to determine the vacancy parameters, stored energy measurements may be used to evaluate accurately the vacancy parameters and the concentrations of vacancies in metals. In the calorimetric method, the experimental procedure consists of rapidly cooling samples and then transferring them into a calorimeter for isothermal annealing. Thus the ener. gy released bE t during annihilation of the vacancies can be determined from the temperature rise /I/ (adiabatic calorimeter) or from the thermal flux measurement /2/ (conduction calorimeter). Such energy can be described experimentally by an Arrhenius plot in specimens quenched from various temperatures Tq : (I)

bEt = A exp(- B/Tq)

If the only quenched-in defects are monovacancies - in

concentration

Co

-

then the

energy stored bE e may be written in the form :

(2~)

~Ee

=

Co

E~v

where Co = exp(Si~k) exp(- E/~kTq). Horeover, if the energy released AEt, which is the quantity experimentally measured, represents exactly the energy stored, then : (2b)

AE e = bE t

From equations (2a) and (2b) : (3)

AE t = Co E fIv

427

C-OMMENTS

428

ON

VACANCY

Using identification monovaeancy

formation

these conditions, calculated

PARAMETERS

of equations

can be determined

the concentration

IN

CALORIMETRIC

(I) and (3)

'

STUDIES

of quenched-in

7, N o . 4

the energy E lfv and the entropy S fI v of

from the Arrhenius plot of in AE t versus vacancies

I/Tq. Under

is given by eq (3), or may be

f

from Eflv and Sty .

For gold, a detailed discussion

has recently be made /3/ of both the assumptions

herent in eqs (2a) and (2b), and this is to be published elsewhere. llke to emphasize that, in calorimetric tion (2 @.

Vol.

studies,

This may affect the determination

AE e # AEt, which is in contradiction

of the parameters

lysis, and in order to evaluate the error reported here an estimation

in-

In this note, we should to equa-

as derived from the above ana-

for these calorimetric

data, we shall give

of AE t.

I~termination of AEt

The quantities tric technique.

of heat involved during the annealing does limit in fact the calorime-

Since the bulk samples should be thin enough to give a sufficient

rate, it follows that a heavier comparatively

quenching

sample can not be used to increase the heat released.

high quench temperatures

Thus

are required to obtain a rather high concentration

of

vacancies. For the range of quench temperatures

used in the calorimetric

methods,

tion of vacancies

does not take place on fixed sinks such as dislocations,

etc : the theory

indicates that the vacancies

can generate their own sinks growing during

the annealing and leading to stable secondary defects ~hich can be observed by electron microscopy

(tetrahedra,

when annealing

dislocation

It is clear that the energy released by annihilation

is in agrement with the contribution

is L (tetrahedron

energy E~ff . The difference

of the vacancy to the energy of

is known, and

edge length or loop diameter

example), the total energy evolved on annealing can be described by the relation (4)

...)

of a vacancy in a cluster is not

the cluster under consideration. that If one asst~nes/the exact nature of secondary defects after annealing that the mean size of these aggregates

loops,

is completed.

to be taken as its own energy of formation but as an effective between these energies

the annihila-

grain boundaries,

for

:

AEt = C O E'iv - C T E(L)

where E(L) is the contribution

of one vacancy to the energy associated with aggregates

of

size L, CT

the total concentration

Further,

: C o -- C T

(5)

stored in these aggregates.

if it is assumed that essentially

led to these secondary defects investigated)

of vacancies

all of the quenched-in

(which is a reasonable

and then eq (4) may be expressed

A%

= co {E~- E(L)}

vacancies

have annea-

assumption under the atandard conditions in the form :

Vol.

7, No.

4

Therefore

COMMENTS ON VACANCY

eq(5)

instead of eq(3)

PARAMETERS

IN CALORIMETRIC

should be applied to calculate

STUDIES

the parameters

429

of for-

mation.

Suac~_~n~faulttetrahedraasseconda~defects In quenched metals, We shall consider tetraedra

several types o f secondary defects are experimentally

only metals

(SFT) are generally

of low stacking fault energy y. In these metals,

of SFT measured

E(L) = (ET)L n (ET)L represents b the nearest

with

It must be emphasized

and recent theorical locations,

n vacancies,

that E(L) is the mean contribution

isotropic,

infinite medium.

for E T in SFT /4/ depends on three terms

energy between dislocations,

In the above equation,

the contribution

(ET)L m a y be calculated

O is the shear modulus,

parameter which can be determine&

approximately

of a vacan-

from the elastic

The most complete : the energy of dis-

and the stacking fault energy.

Gb3 (ET)L = 12~(1--~) bL I 21n ~aL + ( ~2 + 21n 2 + 2 / ~ ( ~ 2

(6)

and

of a vacancy to the energy

- and does not represent

assuming a continuous,

expression

the interaction

:

n = L2/2b 2

into an SFT of edge length L. The value

theory of dislocations

its follows

atom spacing.

(ET)L of SFT - ie the energy per vacancy cy vanishing

after annealing,

the energy of such SFT containing

neighbour

- ~gl2

,,~)}1 +

~ is Poisson's

/~

~(

)2

ratio and a is a core

b y means of atomic calculations

( a ~ 0,5).

Applicationofabovea~lysistog~d For gold, computations

have been made for E T as a function

Taking M

0.3-

of L using eq (6).

:

G = 2,78.10 -3 N.m -2

¢ = 4

b = 2,88.10 -10 m

a = 0,42

Y = 45 .10-3 J.m -2 /5/

0,2-

the results

/l~/

,

are shown on FIGURE I.

0.1 FIGURE

I :VARIATION OF THE ENERGY PER VACANCY

AS A F U N C T I O N O F E D G E L E N G T H F O R S F T .

0 o

5Oo

fault

formed from v a c a n c y clusters.

If L Js the edge length

where

observed.

stacking

lOOO

430

COMMENTS

ON

VACANCY

PARAMETERS

IN C A L O R I M E T R I C

STUDIES

Vol.

7, No.

4

For the quenching temperature range used 1750 - 900 °Cl and for an annealing temperature of about 25 °C, the final edge lengths of SFT are practically constant /6/, /3/, for the specimen purity usually available (Johnson Matthey spectrographically pure gold). Thus if we identify eq. (I) with eq.( 5 ) instead of eq.(3), the determination of ~v from the slope of the experimental straight line in AE t =

f(I/Tq) is not changed. On the other hand, because

of tetrahedra, the entropy and the vacancy concentration determinations should be recalculated. For example the exact concentration C~ can be written as : CA = Co/(I - E(L)/E~) Thus since E(L) < E~v , C~ will be greater than Co. In our experiments, the SFT edge length observed after calorimeter annealing was L = 200 ~. According to the above analysis, our data suggest that the entropy ~

will be

enlarged by 50 % and the vacancy concentrations by about 20 % with regard to the values given by the classical calorimetric method. Under these conditions, the error is larger than the mean accuracy of the calorimetric measurements /3/. Therefore it should be emphasized, in summary, that an accurate determination of vacancy parameters cannot be obtained without a coordination of calorimetric and electron microscopy techniques.

REFERENCES

/1/

W. DE SORBO, Phys. Rev. 11.__77, 444 (1960)

/2/

G. MOYA, L. LAGARDE, Phys. Stat. Sol. 4 2 , 8 3 5 (1970)

/3/

G. MOYA, Th~se Marseille (1973)

/4/

T. JOSSANG, J.P. HIRTH, Phil. Mag. 1.~3 , 657 (1966)

/5/

P.J.C. GALLAGHER~'Symposium of measurement of stacking fault energy" in Metal. Trans. , 1 , 2429 (1970)

/6/

R.W. SIEGEL, Phil. Mag. 13 , 337 (1966)