Applicability of Johnson-Mehl-Avrami model to crystallization kinetics of Zr60Al15Ni25 bulk amorphous alloy
YAN Zhi-jie(闫志杰), DANG Shu-e(党淑娥), WANG Xiang-hui(王祥辉), LIAN Pei-xia(廉培霞)
School of Materials Science and Engineering, Taiyuan University of Science and Technology, Taiyuan 030024, China
Received 3 April 2007; accepted 4 September 2007
Abstract:
The applicability of Johnson-Mehl-Avrami(JMA) model to the crystallization kinetics of Zr60Al15Ni25 bulk amorphous alloy is investigated by differential scanning calorimetry(DSC) under isochronal and isothermal conditions. A criterion xm, at which a defined function z(x) exhibits the maximum value, is introduced to check the validity of JMA model to the kinetics analysis. The value of xm has a constant of 0.632 for JMA model. It is found that the values of xm at different isothermal annealing temperatures (743, 748, 753 and 758 K) are almost near 0.632, which indicates that the isothermal crystallization kinetics can be modeled by JMA equation. However, the values of xm at different heating rates (10, 20, 30 and 40 K/min) are about 0.52, implying that JMA model is not valid to the isochronal crystallization kinetics. The reason why the JMA model is not valid to the isochronal crystallization kinetics is discussed.
Key words:
amorphous alloys; phase transition; thermal analysis; crystallization kinetics; JMA model;
1 Introduction
Amorphous alloys are synthesized when liquid alloys are solidified sufficiently rapidly so that the atomic configuration of liquids is frozen into solids. Overcoming the tendency of conventional liquids to crystallization usually requires extremely high cooling rates only attainable by rapid quenching such as melt- spinning. Since 1989, a new class of amorphous alloys, which can be produced at much lower cooling rates, has emerged[1-7]. These are the so-called bulk amorphous alloys. One of the attractions of the bulk amorphous alloys is that they exhibit a large supercooled liquid region ?Tx (defined as the temperature region between the glass transition temperature Tg and the onset temperature of crystallization Tx), which provides a large experimentally accessible time and temperature window to investigate the crystallization kinetics at the supercooled liquid region[8-9].
Thermal analysis(TA) methods such as DTA or DSC are quite popular for crystallization kinetics analysis of amorphous alloys. An aspect of considerable importance to kinetic analysis is the determination of the kinetics parameters that reflect the crystallization behaviors. The crystallization kinetics based on the TA data is usually modeled by Johnson-Mehl-Avrami(JMA) equation[10-12]:
x(t)=1-exp{-[k(t-τ)]n} (1)
where x is the crystallized volume fraction, t the annealing time, τ the incubation time, n (called as Avrami exponent) a constant related to the behaviors of nucleation and growth, and k a reaction rate constant.
The JMA equation was first derived for transformations under isothermal annealing condition based on the following assumptions[13-15]: 1) homo- genous nucleation or heterogeneous nucleation at randomly dispersed second-phase particles; 2) growth rate of new phase controlled by temperature and independent on time; and 3) low anisotropy of growing crystals. HENDERSON has pointed out that the validity of the JMA equation can be extended under isochronal condition if the entire nucleation behavior completes at the early stage of the transformation, and it becomes negligible afterward[13-14]. Thus, the crystallization ate is defined only by temperature and does not depend on the previous thermal history. Nevertheless, the assumptions above should be carefully considered before JMA model is used for crystallization kinetics analysis. The most popular testing method for isothermal TA data is an inspection of the linearity of JMA plot ln[-ln(1-x)] vs ln(t-τ). In some cases, the JMA plots show straight lines, but the crystallization kinetics cannot be modeled by JMA equation[16]. Thus, a more practical and reliable test method is needed. Based on a function z(x) (seen in the appendix), which can be easily obtained by a simple transformation of DSC data, a simple and practical method to verify the validity of JMA equation is derived to check the value of crystallized volume fraction xm corresponding to the peak of function z(x). For crystallization kinetics that can be modeled by JMA equation, it has been calculated that the value of xm is a constant of 0.632[16]. The detail can be seen in the appendix. In this paper, within the frame of criterion of xm, the applicability of JMA model to the crystallization kinetics of Zr60Al15Ni25 bulk amorphous alloy is discussed under isothermal and isochronal conditions.
2 Experimental
An ingot with nominal composition of Zr60Al15Ni25 was prepared by arc melting a mixture of metals Zr (99.9%, mass fraction), Al (99.99%) and Ni (99.99%) in a water-cooled copper crucible under titanium-gettered argon atmosphere. A plate-like specimen with a cross-section of 1 mm×10 mm and length of 50 mm was produced by suction casting in a copper mold, and its amorphous nature was identified by X-ray diffractometry(XRD) using monochromatic Cu Kα radia- tion. The crystallization kinetics of Zr60Al15Ni25 bulk amorphous alloy was investigated under isothermal and isochronal conditions using a differential scanning calorimeter (NETZCH, DSC 404) under flowing high purity argon. For the isothermal analysis, the amorphous samples were firstly heated to the annealing temperature (743, 748, 753 and 758 K) at a rate of 50 K/min, and then held for a certain period of time until the completion of crystallization. The isochronal DSC plots were recorded at the heating rates of 10, 20, 30 and 40 K/min. Al2O3 and Al pans were utilized for the isochronal and isothermal annealing, respectively. The crystallization products were identified by XRD.
3 Results and discussion
The Zr60Al15Ni25 specimen produced by suction casting in a copper mold is verified to be a single amorphous phase by XRD (not shown here). The isothermal crystallization kinetics of Zr60Al15Ni25 bulk amorphous alloy is investigated by DSC in the supercooled liquid region at 743, 748, 753 and 758 K. All the isothermal DSC traces exhibit a single exothermic peak after a certain incubation period (Fig.1). The detailed isothermal DSC data are listed in Table 1.
Fig.1 Isothermal DSC plots of Zr60Al15Ni25 bulk amorphous alloy at different annealing temperatures
Table 1 Isothermal kinetic parameters of crystallization of Zr60Al15Ni25 bulk amorphous alloy at different annealing temperatures
The exothermic reaction corresponds to the simultaneous precipitation of Al2NiZr6 and AlNi4Zr5 phases (Fig.2(a)). From Table 1, it can be seen that the incubation time τ (defined as the time scale between the time t0 and t1%, t0 is the time to reach the annealing temperature and t1% the time to reach 1% crystallized volume fraction) is relatively short for different annealing temperatures, which is maybe attributed to relatively high annealing temperatures. The value of τ increases slightly when the annealing temperature decreases, however, the exothermic peak width (referred to the time scale between 1% and 95% of transformation into the crystalline state) broadens significantly, indicating a more sluggish crystallization behavior.
Fig.2 XRD patterns of crystallization products of Zr60Al15Ni25 bulk amorphous alloy isothermally annealed at 758 K for 30 min (a) and linearly heated to 1 000 K at heating rate of 40 K/min (b)
The crystallized volume fraction in a given time during crystallization is determined by measuring the partial area of the exothermic peak, and the results are shown in Fig.3. Plotting ln[-ln(1-x)] vs ln(t-τ) using the data x=15%-85%, the isothermal JMA plots at different annealing temperatures are obtained (Fig.4). These plots are nearly straight lines, indicating that the isothermal crystallization kinetics may be modeled by JMA equation. The Avrami exponents n and the reaction rate constants k are calculated by the slopes and intercepts of these JMA lines (Table 1).
Fig.3 Crystallized volume fraction x as function of annealing time t for Zr60Al15Ni25 bulk amorphous alloy at different annealing temperatures
Fig.4 Isothermal JMA plots of crystallization of Zr60Al15Ni25 bulk amorphous alloy at different annealing temperatures
Fig.5 shows the isochronal DSC curves of Zr60Al15Ni25 bulk amorphous alloy at the heating rates of 10, 20, 30 and 40 K/min and the detailed results are listed in Table 2. All the DSC curves show a single exothermic peak, during which Al2NiZr6 and AlNi4Zr5 phases precipitate (Fig.2(b)). The precipitation of complicated compounds Al2NiZr6 and AlNi4Zr5 indicates that substantial redistribution of elements occurs during the crystallization under isothermal and isochronal conditions. The Kissinger plot 
vs 1/Tp is shown in Fig.6. Based on the slope of the Kissinger plot, the effective activation energy Ec is calculated to be 345 kJ/mol. The crystallized volume fraction x in a given time during isochronal crystallization is also determined by measuring the corresponding partial area of the exothermic peak. Plotting ln[-ln(1-x)] vs ln(1/T) using the data x=15%-85%, the isochronal JMA plots at different heating rates are obtained (Fig.7). These plots are obviously non-linear, suggesting that the JMA model is not valid to the isochronal crystallization kinetics. The Avrami exponents obtained by the slopes of these plots are found to be approximately 3.59.
Table 2 Isochronal DSC data of Zr60Al15Ni25 bulk glassy alloy at different heating rates
Fig.5 Isochronal DSC plots of Zr60Al15Ni25 bulk amorphous alloy at different heating rates
Fig.6 Kissinger plot of crystallization of Zr60Al15Ni25 bulk amorphous alloy
Fig.7 Isochronal JMA plots for crystallization of Zr60Al15Ni25 bulk amorphous alloy at different heating rates
The normalized isothermal functions z(x) with respect to the crystallized volume fraction x for the crystallization of Zr60Al15Ni25 bulk amorphous alloy at different annealing temperatures are shown in Fig.8. It can be seen that the values of xm corresponding to the maximum value of isothermal function z(x) locate at the range of 0.61-0.65, which further demonstrates that the JMA model is valid to the isothermal crystallization kinetics. The normalized isochronal functions z(x) with respect to the crystallized volume fraction x at different heating rates are shown in Fig.9. It can be seen that the values of xm of the isochronal function z(x) locate at the range of 0.51-0.55, which further verifies that the isochronal crystallization kinetics can not be modeled by JMA equation.
Fig.8 Normalized function z(x) obtained by transformation of isothermal DSC data of crystallization of Zr60Al15Ni25 bulk amorphous alloy
Fig.9 Normalized function z(x) obtained by transformation of isochronal DSC data of crystallization of Zr60Al15Ni25 bulk amorphous alloy
During the crystallization of an amorphous alloy, the ordered regions in the amorphous phase, as the so- called quenched-in nuclei, maybe provide the nucleation sites for the precipitation of the primary phase[17-18]. When the active size of the quenched-in nuclei is larger than the critical cluster radius at a given temperature, these nuclei may directly grow with time. There exist numerous orders (nanocrystallites) in the Zr60Al15Ni25 amorphous alloys and their average size is about 7 nm [19]. Within the frame of transient nucleation theory, the critical radius of the nucleus during the crystallization of an amorphous alloy is estimated to be about 1 nm[20]. Then, it can be concluded that the size of orders in the Zr60Al15Ni25 bulk amorphous alloy is overcritical. As a result, it is reasonable that the crystallization reaction is activated by the growth of these pre-existing short-range orders.
Under the isothermal condition, the Avrami exponents varying from 1.51 to 4.15 (Fig.4) suggest a diffusion-controlled three-dimensional growth during the crystallization of Zr60Al15Ni25 bulk amorphous alloy. At lower annealing temperatures (743 and 748 K), the Avrami exponents (1.51 and 2.32 respectively) are smaller than 2.5, which indicates that the crystallization is governed by three-dimensional growth with a decreasing nucleation rate[21]. The amorphous state of a multi-component system with significant atomic size difference forms dense random packed atomic configuration[22]. Mobility of atoms in such atomic configuration is obviously difficult. The large effective activation energy for crystallization Ec demonstrates that the atomic diffusion in Zr-Al-Ni system is difficult, especially at low temperature. At the initial crystallization stage, the overcritical orders grow with the nucleation rate of zero. The growth of the overcritical cluster nuclei and formation of new nuclei need the atomic rearrangement. The difficult atomic diffusion at low temperature retards the nucleation and growth, resulting in a decreased nucleation rate and broad exothermic peak width (Fig.2). However, the Avrami exponents at 753 K and 758 K are larger than 2.5, which implies an increased nucleation rate[21]. At higher temperatures, such as 753 K and 758 K, the growth of the overcritical nuclei changes the composition in their neighborhood and results in an enhancement of the nucleation rate adjacent to the growing nuclei because of the easy mobility of atoms, which causes a chain reaction-like process, leading to an increased nucleation rate.
The JMA model can be valid in isochronal crystallization kinetics provided that a new crystalline phase grows from a constant number of nuclei and all nucleation is completed before the crystallization reaction starts. This is the so-called isokinetic crystallization, where the crystallization rate only depends on temperature but not on the previous thermal history[12]. As it is known that the crystallization process of Zr60Al15Ni25 bulk amorphous alloy starts from the growth of pre-existing overcritical orders and is governed by three-dimensional growth with an increased nucleation rate when being annealed at 753 K. In the case of isochronal crystallization, the onset temperatures of crystallization Tx are higher than 753 K (Table 2). Thus, it can be concluded that the nucleation rate during isochronal crystallization process increases with time, since the higher the temperature is, the easier the mobility of atoms is. The nucleation and growth during the isochronal crystallization of Zr60Al15Ni25 bulk amorphous alloy are overlapped. Therefore, the isochronal crystallization kinetics does not fulfill the isokinetic premise, which is the reason why it cannot be modeled by JMA equation.
4 Conclusions
The normalized functions z(x) obtained by transformation of isothermal and isochronal DSC data demonstrate that the JMA model is valid to isothermal crystallization kinetics of Zr60Al15Ni25 bulk amorphous alloy but not to the isochronal crystallization kinetics. From the isothermal kinetics parameters at different annealing temperatures, it is concluded that isothermal crystallization reaction starts from the three-dimensional growth of pre-existing overcritical ordered regions (nanocrystallites), with a decreased nucleation rate at 743 K and 748 K but an increased nucleation rate at 753 K and 758 K. The difference of the nucleation behavior at different annealing temperatures is attributed to the change of the mobility of atoms at different temperatures. During the isochronal crystallization of Zr60Al15Ni25 bulk amorphous alloy, the nucleation and growth overlap, which does not fulfill the isokinetic crystallization that is the premise of the validity for JMA model to the isochronal condition. As a result, the isochronal crystallization kinetics cannot be modeled by JMA equation.
Appendix 1 Basic assumptions of JMA model
There are three basic assumptions inherent in any kinetics analysis of isothermal and isochronal TA data. These assumptions are formulated as follows[16]:
1) The crystallization rate dx/dt is proportional to the measured specific heat flow φ, normalized per sample mass (W/g):
(2)
where ?Hc is the total enthalpy change associated with the crystallization reaction. It is assumed that the crystallized volume fraction x, up to any time t, is proportional to the corresponding partial area of the exothermic peak. Thus the crystallized volume fraction in a given time during crystallization can be calculated by measuring the partial area of the exothermic peak.
2) The crystallization rate can be expressed as a product of temperature dependent reaction rate constant k(T) and x dependent kinetic model function f(x):
(3)
3) The rate constant k(T) in Eqn.(3) follows Arrhenius form:
(4)
where k0 is a pre-exponential factor, Ec the effective activation energy and R the gas constant.
Taking into account the three assumptions above, the kinetic equation for the JMA model can be expressed as:
(5)
in which the kinetic model function f(x) is an algebraic expression of JMA model as:
f(x)=n(1-x)[-ln(1-x)](n-1)/n (6)
The function f(x) should be invariable with respect to procedural parameters, such as sample mass and heating rate (isochronal) or temperature (isothermal).
The validity of the three assumptions above (Eqn.(2)-(4)) should be verified before kinetics analysis of TA data using JMA model.
2 Test criterion xm for JMA model
From the logarithmic form of Eqn.(1), the Avrami exponent n can be obtained from the slope of a JMA plot:
(7)
A similar testing method has also been developed for isochronal TA data. The slope of plot ln[-ln(1-x)] vs ln(1/T) can be expressed as[16]
(8)
The value of Avrami exponent n can be calculated if the effective activation energy Ec is known. Ec can be evaluated by Kissinger equation[23]:
(9)
where β is the heating rate and Tp the temperature of exothermic peak where φ has the maximum value. A Kissinger plot 
vs 1/Tp should be a straight line with a slope of -Ec/R. Then the effective activation energy Ec can be calculated.
The DSC curves φ(t) (isothermal) and φ(T) (isochronal) corresponding to the same kinetic model may be quite different. Moreover, the DSC curves φ(t) and φ(T) depend on the annealing temperature T and heating rate β respectively. However, the function f(x) should be independent on these procedural variables. The function f(x) is proportional to a function z(x), which is defined under isothermal condition as[24]:
z(x)=φ(t) (10)
And under isochronal condition, z(x) is expressed as
z(x)=φT2 (11)
For practical reasons, the function z(x) is usually normalized within the (0 1) range, which exhibits the maximum value at xm. It has been verified that the value of xm is a constant of 0.632 for the JMA model [16]. Then, the applicability of JMA model to a crystallization kinetics can be tested by checking the value of xm.
The criterion of xm has been verified as a simple and practical method to test the applicability of kinetics analysis to JMA model[25]. The error limit of xm by typical TA data is about ±0.02. Thus, the validity of the JMA model to a certain crystallization kinetics can easily be tested by checking the value of xm of the function z(x). If the value of xm locates into the range (0.61 0.65), the crystallization kinetics can be modeled by JMA equation. Reversely, JMA model does not work.
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Foundation item: Project(20051032) supported by the Natural Science Foundation of Shanxi Province, China; Project supported by the Shanxi Provincial Foundation for Leaders of Disciplines in Science and the Doctoral Science Foundation of Taiyuan University of Science and Technology, China
Corresponding author: YAN Zhi-jie; Tel: +86-351-6998062; Fax: +86-351-6998256; E-mail: yanzhijie74@sohu.com
