The Energy-Efficient Processing of Fine Materials by the Micropyretic Synthesis Route

Li, H. P.

doi:https://doi.org/10.1155/2012/727656

Journal of Nanomaterials

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Nanocrystals-Related Synthesis, Assembly, and Energy Applications 2012

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Research Article | Open Access

Volume 2012 | Article ID 727656 | https://doi.org/10.1155/2012/727656

The Energy-Efficient Processing of Fine Materials by the Micropyretic Synthesis Route

H. P. Li¹

Academic Editor: William W. Yu

Received26 Sept 2011

Revised28 Nov 2011

Accepted02 Dec 2011

Published23 Feb 2012

Abstract

Energy-efficient processing of TiB compound with nanowhiskers by micropyretic synthesis is investigated in this paper. Micropyretic synthesis not only offers shorter processing time but also excludes the requirement for high-temperature sintering and it is considered as the one of the novel energy-saving processing techniques. Experimental study and numerical simulation are both carried out to investigate the correlation of the processing parameters on the microstructures of the micropyretically synthesized products. The diffusion-controlled reaction mechanism is proposed in this study. It is noted that nanosize TiB whiskers only occurred when the combustion temperature is lower than the melting point of TiB but higher than the extinguished temperature. The results generated in the numerical calculation can be used as a helpful reference to select the proper route of processing nanosize materials. The Arrhenius-type plot of size and temperature is used to calculate the activation energy of TiB reaction. In addition to verifying the accuracy of the experimental measures, the reaction temperature for producing the micropyretically synthesized products with nanofeatures can be predicted.

1. Introduction

The micropyretic synthesis, or so-called combustion synthesis (CS) or self-propagating high-temperature synthesis (SHS), employs exothermic reaction processing, which circumvents difficulties associated with conventional methods of time- and energy-intensive sinter processing [1–17]. Two basic micropyretic synthesis modes are commonly employed, namely, the wave propagation mode and the thermal explosion mode. In the wave propagation mode, the compacted powders are ignited at a point by a heat source. After ignition, the heat to propagate the combustion wave is obtained from the heat released by the formation of the synthesized product. The unreacted portion in front of the combustion wave is heated by this exothermic heat, undergoes synthesis, the wave propagates, thus causing further reaction and synthesis, as shown in Figure 1. In the thermal explosion mode, the specimen is heated in a furnace. The furnace may be kept at the ignition temperature or the specimen may be heated in the furnace at a predetermined heating rate to the ignition temperature. The micropyretic reaction in this mode may occur more or less simultaneously at all points in the specimen. Although the synthesized product phases obtained by both techniques are similar [1], there may be differences in the amount of residual porosity, final dimensions, and the thermal gradient during the processing.

(a)

(b)

The advantages of micropyretic synthesis techniques include rapid net shape processing and clean products. When compared with conventional powder metallurgy operations, micropyretic synthesis not only offers shorter processing time but also excludes the requirement for high-temperature sintering. Volatile contaminants or impurities may be eliminated as the high temperature combustion wave propagates through the sample, and thus the synthesized products have the higher purity [2, 3]. The steep temperature gradient also gives rise to the occurrence of metastable, nonequilibrium phases or nanosize features, which are not available in the conventional processing [2, 3].

In the past decades, the conventional powder processing routes or other techniques are used to synthesize the materials with the nanofeatures [18–22]. During the nanomaterial processing, there are three main difficulties for making reliable, uniform, nanostructure bulk alloys, including the following (1) The microstructural nonuniformity often occurred in the synthesized product. (2) Energy wastage impacts the cost of production. (3) Human safety is encountered when nanoparticles are processed during the synthesis. Micropyretic synthesis offers the rapid net-shape processing and clean homogeneous product and is thus considered as one of novel processing candidates to process the nano materials [10]. In this study, the micropyretic synthesis is used to process the nanosize materials.

Metal borides are a group of ceramic materials with outstanding and attractive properties for technological applications [8]. Among these materials, Ti-B compound differs with high electrical conductivity, and superconductivity at cryogenic temperatures. The formation of nanosize phase in the Ti-B brittle synthesize product can aid to enhance the mechanical properties dramatically and increase its application. In addition, Ti-B materials can also be synthesized in a net shape by micropyretic synthesis due to the higher exothermic heat. In the previous studies [15–17], we have found that the changes in the processing parameters have the significant impact on the properties of micropyretically synthesized products, including the formation of the nanosize features. Thus, the understanding of the processing parameters is important and can help to select the proper processing nanomaterial route during micropyretic synthesis. In this study, Ti+B micropyretic reaction is chosen to study the effects of the processing parameters on the formation of nano size material. The experimental investigation and numerical calculation are both carried out to study the effects of processing parameters on the formation of nanosize TiB whisker in the micropyretically synthesized products.

1.1. Experimental Procedure

Ti+B micropyretic reaction is chosen to study the effect of processing parameters. Samples are obtained by mixing powders, pressing them into shape and finally combusting the shape by ignition from one end. The particle sizes of titanium and amorphous boron powders are both −325 mesh (<44 μm). In order to retard the propagation velocity and further study the sequential reaction of Ti-B combustion, the larger B particle (−60 mesh, <250 μm) is also chosen in this study. The powders are first tumble mixed for ~10 minutes without the addition of any liquid medium. Subsequently, the well-mixed powders are pressed at 15000 psi (−100 MPa), using a double-acting press and die to form an ASTM-ESM [23] standard specimen. The thickness and longitudinal length of the unreacted green compact are 5 mm and 90 mm, respectively. For obtaining unidirectional wave propagation combustion, the compacted specimen is ignited from one end with an external heating source, which is held against the sample until combustion initiates. The heat source is then removed as the combustion front begins to propagate.

Microstructures are taken by scanning electron microscopy (SEM). For some of the microstructures, energy-dispersive analysis of X-ray (EDAX) is performed to obtain compositional data. X-ray diffraction (XRD) work is carried out in a Siemens diffractometer (model: D500) employing a Cu tube (wavelength: 0.15406 nm) operating at 40 KV and 30 mA. Extremely fine (~100 μm) tungsten-rhenium (W-5% Re and W-26% Re) thermocouples are used to measure combustion temperature and propagation velocity during the combustion reaction. The thermocouples are embedded in the central area of a sample, at a depth of half the sample height. A data acquisition system is used to record the temperature at every 0.1-second interval. The combustion temperature is defined as the highest temperature during the combustion reaction. The average propagation velocity is calculated from the known distance between the thermocouples and the time lapse between the first signs of propagation of each thermocouple.

1.2. Numerical Simulation

During the passage of a combustion front in the micropyretic reaction, the energy equation for transient heat conduction, including the source term, containing heat release due to the exothermic reaction is given as [6, 12, 13] Each symbol in the equation is explained in the nomenclature section. The reaction rate, , in (1) is given as

In this study, a numerical calculation for (1) is carried out with the assumption of the first-order kinetics. In (1), the energy required for heating the synthesized product from the initial temperature to the adiabatic combustion temperature is shown on the left-hand side. The terms on the right-hand side are the conduction heat transfer term, the surface heat loss parameter, and the heat release due to the exothermic micropyretic reaction, respectively. The previous two-dimension study [12] has indicated that the conduction heat transfer and surface heat loss are so small as compared with the exothermic heat. Thus, the surface heat loss is assumed to be radically Newtonian and is taken to be zero in this study.

A middle-difference approximation and an enthalpy-temperature method coupled with Gauss-Seidel iteration procedure are used to solve the equations of the micropyretic synthesis problems. In the computational simulation, a one-dimensional sample of 1 cm long is divided into 1201 nodes (regions) to calculate the local temperature. This one-dimensional numerical model assumes the following sequence of events: (1) the specimen is gradually heated by a surface heat source; (2) the reaction is ignited and the combustion front propagates along the specimen; (3) there is a cooling source at one end. The choice of 1 cm sample length is only for computational purpose, and the simulation results are applicable to practical experimental conditions. The proper initial conditions are used to initialize the temperatures and enthalpies at all nodes. At time = 0, the temperatures are taken to be the same as the substrate temperature ( (300 K) and = 0). The energy is gradually added at the ignition node in very small time steps until the combustion front starts to propagate.

The various microscale events, that is, local processes such as warming of the sample, melting of lower refractory reactant, formation of product, and cooling of the sample at one end, are included in this calculation procedure. Depending on the values of the temperature and enthalpy occurring in the reaction, the proper thermophysical/chemical parameters are considered and the limits of the reaction zone are determined for each node in the numerical calculation. At any given time, the fraction reacted and enthalpy of the current iteration are calculated from the previous fraction reacted and enthalpy of the earlier iteration. The range of the enthalpy as well as the molar ratio among each material for each node is thus determined, and the values of temperature, density, and thermal conductivity at each node can be further calculated in appropriate zone.

The various thermophysical/chemical parameters, such as thermal conductivity, density, and heat capacity of the reactants and product, are assumed to be independent of temperature, but they are different in each state. The average values of these parameters vary as the reaction proceeds, depending upon the degree of reaction. The parameter values used in the computational calculation are shown in Table 1 [24] and Table 2 [25, 26]. In this study, the combustion temperature is defined as the highest reaction temperature during micropyretic synthesis, and the propagation velocity is the velocity of the combustion front propagation. In addition, the higher preexponential factor () value, 1.0 × 10¹⁰ 1/s, is used to be capable of illustrating the variation of the propagation velocity for the Ti-B micropyretic reaction.

2. Results and Discussion

2.1. Ti-B Micropyretic Reaction

It has been proposed that the micropyretic/combustion synthesis includes the diffusion and the capillary-controlled reaction mechanisms, which are dependent on the size of the reactant particle [27–29]. Following the study of Nekrasov et al. [29], the diffusion control is dominant when where and are the diameters of the particle sizes for the low melting point component and high melting point component, respectively. The other symbols and the values of the variables used for calculating (3) are shown in Table 3 [24–26, 30]. The Ti particle (low melting component) size threshold between the diffusion-controlled and the capillary-controlled combustion propagation may be thus calculated using (3). Employing (3), we note that the diffusion control can take place when the B size (diameter) should be higher than 0.14 nm for 30 μm Ti. The boron sizes we used in this study are in the microscare (−60 mesh and −325 mesh, <250 μm and <44 μm) and are much higher than the correspondingly calculated critical size. Thus the studied mixtures are expected to be all in the range of diffusion-controlled combustion.

For investigating the possible titanium boride reaction mechanism in the Ti-B binary system, a sample with larger B particles (−60 mesh (<250 μm)), which propagates at a lower velocity, is intentionally extinguished during the propagation. It is inferred from microstructures that as the combustion starts, the unreacted portion in front of the combustion front is preheated by the released energy. The temperature of the unreacted portion is increased to a high level, melting the less refractory phase (Ti). The molten Ti encapsulates the nonmelting B particles (Figure 2). The resultant increase in the contact area between Ti and B significantly increases the reaction kinetics. The reacted product subsequently forms a layer on the surface of the nonmelting B particle. The exothermic heat of the product formation is released and conducts to unreacted materials, which in turn react, continuing the chain reaction.

From the diffusion-control mechanism theory and the observed microstructures (Figure 2), we propose the following reaction sequences for Ti-B reaction. (1) The Ti particles first melt and flow around the B particles. (2) The contact efficiency of B particles with the Ti liquid is now increased and the molten Ti ignites the rapid reaction. (3) An intermediate complex forms. (4) The Ti atoms diffuse from the melt, across the complex, to readily react with the B particle at its surface. (5) The intermediate complex of reaction is dissolved on the Ti-liquid side. Fresh new intermediate complex phase is formed between the intermediate complex phase and B particle at such a rate that the thickness of the complex is a constant. (6) The final Ti-B stoichiometric product is then precipitated from the molten liquid.

Figures 3(a) and 3(b) show the microstructures for the Ti-B reactions with the different compositions. Note from Figure 3 that microstructures are significantly changed when the composition is varied from 10 wt.% B to 25 wt.% B. The formation of the nanosize feature is only observed in the composition with 10 wt.% B. The average measured propagation velocity for the composition with 25 wt.% B (>20 cm/s) is much higher than that for composition 10 wt.% B ( cm/s). The combustion temperature for the composition with 25 wt.% B exceeds the upper limit of thermocouples, and the combustion temperature is increased with the increase in the propagation velocity, as shown in Table 3. These experimental demonstrations show that the changes in the processing parameters influence the combustion temperature and propagation velocity, further altering the microstructures and properties of the synthesized products. To understand the processing parameters as nanosize structures form, the computer simulation is then used to aim towards an understanding.

(a)

(b)

2.2. Numerical Study Is Used to Forecast the Formation of Nanosize Structures

The previous experimental and numerical studies [12, 15, 16] have shown that the processing parameters, including the initial temperature, reactant particle size, diluents, compact density, compositions, exothermic heat, and activation energy have a significant impact on the reaction parameters, like propagation velocity and combustion temperature. A change in the reaction parameters has significantly influenced the properties of the synthesized products. It is noted that the combustion temperature and propagation velocity are increased as increasing the initial temperature or exothermic heat or are decreased as increasing the reactant size, activation energy, or amount of the diluents.

Figure 4 shows the numerical calculating results for the temperature-time plots for the compositions with the different processing parameters (different values of activation energy). The micropyretic reactions are ignited by ignition power (per gram) of 175 Joule/(ms·g) at the position 0 cm, and the heating sources are removed immediately after the combustion front has been ignited. The interval time between two consecutive time steps (profiles) in Figure 4 is 0.001 s. It is found from Figure 4(b) that the combustion front takes 21.04 ms to start propagating for the Ti-B micropyretic reaction with the reported experimental activation energy (318 KJ/mole) [27]. This ignition time interval corresponds to the ignition energy of 3682.0 Joule/g. Figure 4(b) also displays an alternating increase and decrease in the temperature and propagation velocity during the combustion front propagation, indicating that the combustion front for Ti-B micropyretic reaction propagates in an unstable oscillatory manner. When 80% of reported experimental activation energy value is taken in the numerical calculation, the propagation manner is noted to change from unstable manner to stable manner; in addition, the ignition time is reduced from 21.04 ms to 16.38 ms, which corresponds to the ignition energy of 2866.5 Joule/g (Figure 4(a)). When 120% of reported experimental activation energy is taken in the calculation, the ignition time is increased to 25.66 ms (corresponding to the ignition energy of 4490.5 Joule/g) and the combustion front extinguishes immediately after the start of propagation (Figure 4(c)).

(a)

(b)

(c)

Figure 4

Time variations of the combustion front temperature along the TiB₂ specimen with the preexponential factor of 1 × 10¹⁰ s⁻¹. The interval time between two consecutive time steps (profiles) is 1.0 ms. The ignition power is taken as 175 Joule/(ms·g) in the numerical calculation. The activation energy in (a), (b), and (c) are taken as 254.4 KJ/mole (80% of reported experimental value) [27], 318.0 KJ/mole (reported experimental value), and 381.6 KJ/mole (120% of reported experimental value), respectively.

It is known that the decrease in the propagation velocity reduces the oscillating combustion temperature. A further decrease in the velocity may extinguish the propagation of the combustion front. The study of Borovinskaya et al. [8] also shows the oscillating patterns for Ti- (and Ta-, Nb-, Zr-) B reaction. Thus, the above results generated from the above numerical demonstrations indicate that the nanowhisker formation can be acquired only at the low reaction temperature but without stopping the chain reaction. This study next tries to select the proper reaction temperature to synthesize the nanosize material by changing the reactant compositions.

2.3. Selection of the Proper Processing Parameters to Synthesize Nanosize Products

Figure 5 shows the SEM morphologies of the synthesized products with different boron content. It is noted from Figure 5 and Table 4 that the sizes of the whiskers are decreased with the decrease in the combustion temperature. The new nonwhisker structures are observed when the combustion temperature exceeds 2100 K. It is expected that the average measured combustion temperature of composition with 25 wt.% B is much higher than the melting point of TiB phase. The TiB whiskers may be melted and then solidified. The nonwhisker microstructure is thus formed.

(a)

(b)

(c)

The whisker structures are further analyzed by XRD. The X-ray patterns show that the whisker structures tend to be the TiB phase. Similar Ti-B whisker morphologies have also been observed in several studies [31–34]. In the study of Andrievskii et al. [31], it was shown that TiB₂ (hexagona1 type) and TiB (orthorhombic type) are probably characterized by anisotropy of surface energy, and consequently the grains are expected to be faceted. Hashimoto et al. [32] found that at sintering temperatures of 1373 K, and 1473 K the needle- or fiber-type TiB₂ precipitates when the coarse B powder (~150 μm) is chosen. Hyman et al. [33] performed extensive as-cast-binary as well as TEM studies on the formation of TiB and TiB₂ in the ternary Ti-Al-B system. It was shown that the crystal structures of both TiB and TiB₂ are based on the same building block and have the same needle-like morphology [33]. Similar whisker-like structures are also observed on the Ti-B compounds by micropyretic synthesis [34]. Yang et al. [34] show that the morphologies of the combustion synthesized Ti-B compounds varied from flake type to whisker type, depending on boron content.

2.4. Robust Check of the Error of the Measured Sizes and Temperatures

Arrhenius-type plot of size and temperature is used to calculate the activation energy of Ti-B reaction. As compared with the reported experimental value, the calculated activation energy can be used to verify the accuracy of the measured size and temperature in this study. The diameters of the TiB whisker-type structures are noted to increase when the combustion temperature is raised by changing the composition. The correlation of the whisker diameter with the temperature is thus used to calculate the activation energy [35–38]. The general relation between the whisker/grain size and the temperature is expressed as [35, 36] where is the grain size or whisker diameter, is the activation energy for the whisker growth, is the combustion temperature, and is the universal constant (= 8.314 J/mole/K). As employing (4), the activation energy for TiB whisker growth is determined from the plot of and . From an Arrhenius-type plot in Figure 6, the activation energy for the whisker growth is calculated to be 231 KJ/mole. As compared with the reported values for TiB combustion, 230 KJ/mole [39] or 251 KJ/mole [40], which was approached from the combustion wave velocity and temperature profile investigation, respectively, the calculated value for the whisker growth is in good agreement with the reported values for the Ti-B combustion, verifying the accuracy of the measured size and temperature in this study.

In addition, from the Arrhenius-type plot of diameter and measure combustion temperature, we can also forecast the reaction temperature for the nanosize whisker. Note from the calculated results that the <10 nm TiB whisker starts to form when the combustion temperature is decreased to 1500 K.

3. Summary and Conclusions

Processing of TiB compound by micropyretic synthesis is carried out in this study. Experimental study and numerical simulation are both used to investigate the correlation of the processing parameters on the microstructure of the synthesized products. It is noted that nanosize TiB whisker is expected to occur when the combustion temperature is lower but higher than the extinguish temperature. The results generated in the numerical calculation can be used as a helpful reference to select properly the processing route of producing nanosize features product. The Arrhenius-type plot of size and temperature is also used to calculate the activation energy of TiB reaction. The calculation activation energy is in a good appointment with the reported value, verifying that the accuracy of the experimental measures of the grain size in this study. In addition, the Arrhenius-type plot can be used to forecast the combustion temperature for producing nanosize TiB whisker.

Nomenclature

:	Heat capacity, Jkg⁻¹ K⁻¹
:	Activation energy, Jmole⁻¹
:	Surface heat transfer coefficient, Jm⁻² K⁻¹ s⁻¹
:	Preexponential factor, s⁻¹
:	Exothermic heat of reaction, Jmole⁻¹
:	Universal gas constant, Jmole⁻¹ K⁻¹
:	Temperature, K
:	Initial temperature of the unreacted compact, K
:	Time, s
:	Dimensional coordinate, m
:	Diameter of the specimen, m.

Greek Letters

:	Thermal conductivity, Jm⁻¹ s⁻¹ K⁻¹
:	Reaction rate, s⁻¹
:	Density, km⁻³
:	Reacted fraction.

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Copyright © 2012 H. P. Li. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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