Precipitation morphology and kinetics of T-Al6Mg11Zn11 intermetallic phase in Al–Mg–Zn ternary alloys

2021 ◽  
Vol 139 ◽  
pp. 107364
Author(s):  
Naoki Takata ◽  
Rikito Takagi ◽  
Ruoqi Li ◽  
Hiroki Ishii ◽  
Asuka Suzuki ◽  
...  
Author(s):  
Mohammad Faizan ◽  
Guo-X. Wang

Soldering has become an indispensable joining process in the electronic packaging industry. The industry is aiming for the use of environment friendly lead-free solders. All the lead-free solders are high tin-containing alloys. During the soldering process, an intense interaction of metallization on PCB and tin from the solder occurs at the metallization/solder interface. Intermetallic compound (IMC) is formed at the interface and subsequently PCB bond-metal (substrate) is dissolved into the molten solder. In the present study the terms bond-metal and substrate will be used interchangeably and the term 'substrate' refers to the top layer of the PCB which comes in contact with the molten solder during soldering reaction. Thickness of the intermetallic phase formed at the joint interface and amount of substrate lost is critical in achieving reliable solder joints. During the wet phase of soldering process, the IMC does not grow as layered structure; rather it takes the shape of scallops. The growth of scalloped IMC during the solder/substrate interaction entails complicated physics. Understanding of the actual kinetics involved in the formation of IMC phase is important in controlling the process to achieve desired results. This paper presents theoretical analysis of the kinetics involved in the formation of the scalloped intermetallic phase. The intermetallic phase growth is experimentally investigated to support the underlying kinetics of the process. Numerical model has been suggested to translate the physics of the process. The model is based on the basic mass diffusion equations and can predict the substrate dissolution and IMC thickness as a function of soldering time.


2013 ◽  
Vol 212 ◽  
pp. 137-140 ◽  
Author(s):  
Janusz Cebulski ◽  
Stanisław Lalik

The aim of this paper was to determine the resistance to high-temperature corrosion in atmosphere of air for alloy Fe-40Al-5Cr-0.2Ti-0.2B. Corrosion tests were conducted in temperatures from 600 to 900°C in time from 2 to 64 hours. Conducted tests have shown a slight increase of weight of samples in periods of time which followed. Increase of weight is connected with corrosion products in the form of passive oxides which form on the surface of the alloy. Kinetics of corrosion processes has parabolic course in tested temperature range which proves the formation of passive layers of corrosion products on the surface of samples. Heat resistance of the alloy on intermetallic phase matrix FeAl brings about potential possibilities to apply this alloy as a material meant for work in elevated and high temperatures in the environment which includes oxygen.


2011 ◽  
Vol 1295 ◽  
Author(s):  
Ayan Bhowmik ◽  
Hon Tong Pang ◽  
Steffen Neumeier ◽  
Howard J. Stone ◽  
Ian Edmonds

ABSTRACTThe phase equilibria and oxidation resistance of alloys lying near the Cr-rich end of the Cr- Ta-Si system have been investigated. Samples were prepared by arc-melting and homogenized at 1300°C for 500hrs. Identification of the phases present and their compositions were carried out using x-ray diffraction and electron probe micro-analysis and the ternary phase diagram on the Cr-rich end was plotted. A three-phase equilibria was found to exist between an A2 Cr-solid solution, a hexagonal Laves phase and the A15 Cr3Si intermetallic phase for alloys with higher contents of Si.Thermo-gravimetric analysis of the alloys at 1100°C demonstrated an improvement in the oxidation resistance of the ternary alloys with increasing Si-content. The microstructures of the oxidized samples revealed the formation of a thick chromia layer on top of a Cr,Ta-mixed oxide layer and an internal oxidation zone for all the alloys. A protective silica layer was not observed to form in any of the alloys tested.


1994 ◽  
Vol 364 ◽  
Author(s):  
Mark Asta ◽  
Alim Ormeci ◽  
John M. Wills ◽  
Robert C. Albers

AbstractThe stability of bcc-based phases in the Ti-Al-Nb alloy system has been studied from first-principles using a combination of ab-initio total energy and cluster variation method (CVM) calculations. Total energies have been computed for 18 binary and ternary bcc superstructures in order to determine low temperature ordering tendencies. From the results of these calculations a set of effective cluster interaction parameters have been derived. These interaction parameters are required input for CVM computations of alloy thermodynamic properties. The CVM has been used to study the effect of composition on finite-temperature ordering tendencies and site preferences for bcc-based phases. Strong ordering tendencies are observed for binary Nb-Al and Ti-Al bcc phases as well as for ternary alloys with compositions near Ti2AlNb. For selected superstructures we have also analyzed structural stabilities with respect to tetragonal distortions which transform the bcc into an fcc lattice. Instabilities with respect to such distortions are found to exist for binary but not ternary bcc compounds.


2002 ◽  
Vol 43 (2) ◽  
pp. 271-276 ◽  
Author(s):  
Yoshihiro Suwa ◽  
Yoshiyuki Saito ◽  
Kazumi Ochi ◽  
Takahiro Aoki ◽  
Kanako Goto ◽  
...  

1998 ◽  
Vol 514 ◽  
Author(s):  
X. Federspiel ◽  
F. Voiron ◽  
M. Ignat ◽  
T. Marieb ◽  
H. Fujimoto

ABSTRACTThe knowledge of the reaction kinetics which can occur at an interface of a couple of materials, remains a crucial issue to establish the structural limits of a diffusion barrier intended for microelectronic structures.In the past years, the interfacial reactions activated at an interface of a couple of materials, as for example aluminum and titanium, have been analyzed extensively using different experimental tools, as for example: Ruthreford Back Scattering (thickness determination) and Differential Scanning Calorimetry (DSC). Then, these experimental methods were useful to deduce parameters, characterizing the interfacial reactions in bulk samples: apparent activation energies, enthalpy of formation. Because in thin films, the kinetics of the reactions that can be activated at an interface will be different; we studied interfacial reactions in submicronic Al/Ti layers.Taking advantage of the accuracy of the DSC (reaction rate determinations and detection of earlier stages of intermetallic phase formation), our experimental approach consisted in a series of isothermal and non-isothermal DSC experiments on submicron Al/Ti layered structures. From the reaction rate determination, analytical methods as the Kissinger Ozawa approach were used, to determine the apparent activation energies of the phase formation. Also the results allowed to model and discuss the first steps of the interfacial reaction.


2008 ◽  
Vol 1128 ◽  
Author(s):  
H. Zapolsky ◽  
J. Boisse ◽  
R. Patte ◽  
N. Lecoq

AbstractThe coarsening kinetics of γ’ precipitates in binary and ternary Al3Sc1-xZrx alloys is studied by using the two- and three-dimensional phase-field simulations. Our focus is on the influence of diffusion coefficients of Sc and Zr atoms on the transformation path kinetics from disordered f.c.c. matrix to two phases equilibrium state with γ’ precipitates and f.c.c. disordered matrix. Our simulation results demonstrate that in the case of binary alloys taking into account the concentration dependence of the mobility of atoms decreases the coarsening rate. In the case of ternary alloys we show that the Al3Sc particles precipitate first following by appearance of a Zr-rich shell. Our simulations results are in good agreement with experimental observations.


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