Self-propagating Reaction Research Articles

Demonstrating the Simplicity and In Situ Temperature Monitoring of the Mechanochemical Synthesis of Metal Chalcogenides Suitable for Thermoelectrics.

Mechanochemical synthesis is an extremely useful strategy to reach thermoelectric materials due to its solvent-free one-step character, as the targeted thermoelectricity (TE) materials in a nanocrystalline format can be prepared by mere high-energy milling of elemental precursors. Nevertheless, the subsequent densification method (e.g., spark plasma sintering or hot pressing) is required afterward, similarly to other synthetic methodologies. In this study, the simplicity of mechanochemical synthesis ispresented for two selected metal chalcogenides, namely copper sulfide (Cu1.8S, digenite) and tin selenide (SnSe, svetlanaite), which are known for high ZT values. These compounds can be prepared via a mechanically induced self-propagating reaction (MSR), which is a combustion-like process instantly yielding the products in a very short timeframe (within 1 min). The occurrence of MSR can be well-tracked by in situ temperature monitoring since an abrupt temperature increase occurs at the moment of MSR. We have developed a device which is capable of monitoring the temperature inside the milling jar every 80 ms during planetary ball milling, and it is therefore possible to very precisely track the moment of MSR ignition. The developed device presents an improvement in the monitoring capabilities in comparison with commercially available analogs. This contribution aims to provide a visual insight into all steps, with simple high-energy ball milling of elements to reach TE materials and in situ temperature monitoring being the central points.

Enhanced Multifaceted Properties of Nanoscale Metallic Multilayer Composites.

This study explored the fascinating field of high-performance nanoscale metallic multilayer composites, focusing on their magnetic, optical, and radiation tolerance properties, as well as their thermal and electrical properties. In general, nanoscale metallic multilayer composites have a wide range of outstanding properties, which differ greatly from those observed in monolithic films. Their exceptional properties are primarily due to the large number of interfaces and nanoscale layer thicknesses. Through a comprehensive review of existing literature and experimental data, this paper highlights the remarkable performance enhancements achieved by the precise control of layer thicknesses and interfaces in these composites. Furthermore, it will discuss the underlying mechanisms responsible for their exceptional properties and provide insights into future research directions in this rapidly evolving field. Many studies have investigated these materials, focusing on their magnetic, mechanical, optical, or radiation-tolerance properties. This paper summarizes the findings in each area, including a description of the general attributes, the adopted synthesis methods, and the most common characterization techniques used. The paper also covers related experimental data, as well as existing and promising applications. The paper also covers other phenomena of interest, such as thermal stability studies, self-propagating reactions, and the progression from nanomultilayers to amorphous and/or crystalline alloys. Finally, the paper discusses challenges and future perspectives relating to nanomaterials. Overall, this paper is a valuable resource for researchers and engineers interested in harnessing the full potential of nanoscale metallic multilayer composites for advanced technological applications.

Investigating Enhanced Microwave Absorption of CNTs@Nd0.15-BaM/PE Plate via Low-Temperature Sintering and High-Energy Ball Milling.

Composite plates comprising a blend of rare earth neodymium-(Nd) doped M-type barium ferrite (BaM) with CNTs (carbon nanotubes) and polyethylene WERE synthesized through a self-propagating reaction and hot-pressing treatment. The plates' microscopic characteristics were analyzed utilizing X-ray diffraction (XRD), Fourier transform infrared spectrophotometry (FTIR), thermo-gravimetric analysis (TGA), Raman, and scanning electron microscopy (SEM) analytical techniques. Their microwave absorption performance within the frequency range of 8.2 to 18 GHz was assessed using a vector network analyzer. It showed that CNTs formed a conductive network on the surface of the Nd-BaM absorber, significantly enhancing absorption performance and widening the absorption bandwidth. Furthermore, dielectric polarization relaxation was investigated using the Debye theory, analyzing the Cole-Cole semicircle. It was observed that the sample exhibiting the best absorbing performance displayed the most semicircles, indicating that the dielectric polarization relaxation phenomenon can increase the dielectric relaxation loss of the sample. These findings provide valuable data support for the lightweight preparation of BaM-based absorbing materials.

Average dose rate is the primary determinant of lipid peroxidation in liposome membranes exposed to pulsed electron FLASH beam

BackgroundLipid peroxidation, a self-propagating chain reaction that oxydates lipid molecules, contributes to harmful effects of ionizing radiation. A decrease in peroxidation at higher dose rates could play a role in the FLASH sparing effect. PurposeWe explored how lipid peroxidation induced by FLASH (>100 Gy/s) and conventional (CONV, <0.2 Gy/s) radiation depends on lipid concentration and content of polyunsaturated fatty acids (PUFA). Additionally, we investigated the correlation between the lipid peroxidation and the main beam parameters characterizing pulsed electron beams, namely the dose per pulse (DRp) and the average dose rate (DRav). MethodsWe employed phosphatidylcholine (PC) liposomes as a model of biological membranes. Suspensions of liposomes containing different proportions of linoleic acid (LA) were prepared at various concentrations and irradiated at FLASH and CONV dose rates. Additionally, the liposomes were exposed to beams characterized by diverse combinations of DRp and DRav. The extent of lipid peroxidation was assessed by monitoring oxygen consumption (ΔpO2) and measuring the yield of malondialdehyde (MDA), and in certain instances, of lipid peroxides (LOOH). ResultsRegardless of the radiation dose, liposome concentration or LA content, ΔpO2 and the yield of MDA were significantly lower for FLASH than for CONV irradiation. Increase in the proportion of readily oxidizable LA in the lipid had negative effect on the MDA yield but correlated positively with ΔpO2 and LOOH yield. Exposing liposomes to beams operating at different pulse repetition frequencies, while keeping the total dose and DRp constant, resulted in markedly different ΔpO2 and MDA yields. In contrast, DRav was found to exhibit stable correlation with both MDA yield and ΔpO2. ConclusionsIrradiation at FLASH dose rates produces lower yield of lipid peroxidation in PUFA-containing artificial PC membranes than CONV irradiation under all tested conditions. Time-averaged dose rate, in contrast to pulse dose rate, was the critical parameter determining the level of lipid peroxidation induced by pulsed electron beams.

Production of iron triad-based colored spinels by the self-propagating high-temperature synthesis

Blue, green, and khaki spinels were produced by self-propagating high-temperature synthesis (SHS) using Co3O4–ZnO–Mg(NO3)2·6H2O–Al(OH)3–Al, Ni2O3–ZnO–Cr2O3–Al(OH)3–Al, and Co2O3–Fe2O3–Al(OH)3–Al mixtures. The composition of the synthesis products was characterized by X-ray diffraction and IR spectroscopy. The oxides Co3O4, Co2O3, ZnO, Ni2O3, Cr2O3, Fe2O3, and aluminum hydroxide Al(OH)3 were used for the synthesis. Fuel was provided by aluminum powder (ASD-4). The spinel-type ceramic pigments were synthesized using layer-by-layer combustion, which involves two parallel exothermic reactions: aluminum oxidation and aluminothermic reactions. The fast self-propagating reactions and high synthesis temperatures rapidly destroy the structure of Al(OH)3 hydroxide in the starting mixture, producing gaseous reaction products that prevent the sintering of the spinels. The surface morphology of pigment powders and their composition was studied using a Quanta 3D 200i, FEI Co. scanning electron microscope and a Philips SEM 515 scanning electron microscope equipped with a local energy dispersive X-ray analysis (EDAX). The particle size of the synthesized spinels was approximately 1–5 μm. Colored spinels powders obtained by the SHS process can be used as ceramic pigments.

Sub-millisecond lithiothermal synthesis of graphitic meso–microporous carbon

Porous carbons with concurrently high specific surface area and electronic conductivity are desirable by virtue of their desirable electron and ion transport ability, but conventional preparing methods suffer from either low yield or inferior quality carbons. Here we developed a lithiothermal approach to bottom–up synthesize highly meso–microporous graphitized carbon (MGC). The preparation can be finished in a few milliseconds by the self-propagating reaction between polytetrafluoroethylene powder and molten lithium (Li) metal, during which instant ultra-high temperature (>3000 K) was produced. This instantaneous carbon vaporization and condensation at ultra-high temperatures and in ultra-short duration enable the MGC to show a highly graphitized and continuously cross-coupled open pore structure. MGC displays superior electrochemical capacitor performance of exceptional power capability and ultralong-term cyclability. The processes used to make this carbon are readily scalable to industrial levels.

Highly Exothermic and Fast Mechanochemical Redox and Intercalation Reactions of V2O5 with Sodium Hydride.

Vanadium oxides exhibit promising characteristics for electrochemical energy storage, owing to their capability to switch between different oxidation states, in combination with the incorporation of alkali metals. Here, we report on a systematic investigation of the mechanochemical reduction of V2O5 with NaH. In contrast to conventional high-temperature synthesis methods, the mechanochemical reaction occurs already after a few minutes. We observed a mixture of different (sodium) vanadium oxides with vanadium oxidation states ranging from +III to +V. Remarkably, these highly exothermic self-propagating reactions occur even within a rudimentary pistil-mortar setup. Hereby, the hydride concentration has a greater effect on the final sample composition than the milling time. In general, higher percentages of sodium vanadates are formed instead of vanadium oxides, and the lower oxidation states of vanadium are accessible with increasing amounts of NaH. Theoretical calculations confirm these experimental observations and emphasize the central role of sodium vanadates, especially with vanadium in the +V oxidation state, in carrying out the observed exothermic reactions. This comprehensive study sheds light on the mechanochemical reduction of vanadium oxides and underlines their potential for further development of electrochemical energy storage systems.

Modelling reaction transfer velocities in disconnected compact heterogeneous multilayer reactive material systems

The tuning of the self-propagating reaction is studied theoretically by introducing a non-reactive material between two reactive material elements. For the study, the Ni/Al bilayer system was chosen. The Ni/Al elements were placed on a silicon wafer covered with a 1-µm-thick silicon dioxide. The spaces between the multilayer reactive material elements were filled with different non-reactive materials covering a wide range of thermal properties. On top of this heterogeneous layer, a 1-µm-thick sealing layer was placed consisting of the filler material. The carried out two-dimensional simulations demonstrated that embedding material allows to scale the ignition transfer time and the heat propagation velocity. For example, for a transfer length of 1 µm, the ignition time can be tuned from nano- to microseconds. Consequently, in contrast to previous results embedding materials allow scaling the properties of the self-propagating reaction in heterogeneous reactive material systems.Graphical abstract

Mechanochemical ignition of self-propagating reactions in equimolar Al-Ni powder mixtures and multilayers.

This work addresses a long standing question in the field of mechanochemistry, namely the role of mesostructure in the initiation of self-propagating high-temperature reactions in exothermic chemical systems, commonly referred to as ignition. In an attempt to find robust evidence in this regard, we compare the ignition behaviour of equimolar Al-Ni powder mixtures and equimolar Al-Ni multilayers. To achieve the best possible control of experimental conditions and allowing high reproducibility, we used elemental powders sieved in the range between 20 μm and 44 μm, and multilayers with bi-layer thickness between 10 nm and 800 nm. We carried out systematic ball milling experiments involving pristine powder mixtures and multilayers as well as a mix of pristine material and material prone to ignition suitably prepared. Experimental findings suggest that pristine powder mixtures and multilayers with bi-layer thickness of 240 nm have analogous ignition behaviour. Along the same lines, data suggest that pristine powder mixtures undergo ignition when they attain a mesostructure similar to that of multilayers with bi-layer thickness of 10 nm.

Preparation of Ti3SiC2-based diamond composites by Ni–Al assisted self-propagating reaction of Ti–SiC–C system in microwave field

In this paper, the self-propagating reaction of the Ti–SiC–C system for synthesising Ti3SiC2-based diamond composites is ignited by the combustion of Ni–Al alloy powders in a microwave field. The heating curves of Ni–Al-assisted microwave sintering show that the self-propagating reaction could be successfully ignited after heating samples to 685.2 °C in a microwave field for 456 s. This finding indicates that ignition could occur at temperatures below the diamond graphitisation temperature (727 °C). X-ray diffraction analysis indicates that the sintered samples primarily comprise Ti3SiC2, TiC, Ti5Si3 and C. Scanning electron microscopy coupled with energy dispersive spectroscopy observations demonstrates that the diamond grains are tightly bonded with the surrounding matrix and are intact. The best wear ratio of 302.26 was obtained for the Ti3SiC2-bonded diamond composite when the diamond grain size was 140/170 mesh and the molar ratio of Ti, SiC and C was 3:1.1:0.9.

Mechanically induced self-propagating reactions (MSRs) to instantly prepare binary metal chalcogenides: assessing the influence of particle size, bulk modulus, reagents melting temperature difference and thermodynamic constants on the ignition time

Mechanically induced self-propagating reactions (MSRs) of metal chalcogenides can be completed within few minutes and seem to be partly governed by particle size distribution and bulk modulus of the reagents.

Electrodeposition of Reactive Aluminum-Nickel Coatings in an AlCl3:[Emim]Cl Ionic Liquid Containing Nickel Nanoparticles

The electrodeposition of reactive aluminum-nickel dispersion coatings was performed by pulsed direct current (PDC) onto copper substrates in the ionic liquid 1.5:1 AlCl3:[EMIm]Cl (1-Ethyl-3-methylimidazolium chloride). A cathodic current density of 15 mA/cm2 was used with two different frequency (f)/duty cycle (r c) combinations, i.e., f= 0.33 Hz/ r c= 0.33 (t on= 1 s, t off= 2 s) and f= 0.05 Hz/ r c= 0.5 (t on= 10 s, t off= 10 s). Several electrochemical techniques like Cyclic Voltammetry, Electrochemical Impedance Spectroscopy and Open Circuit Potential measurements were used besides X-Ray Diffraction, Confocal Microscopy, Scanning Electron Microscopy, Atomic Absorption Spectroscopy and 27Al/1H Nuclear Magnetic Resonance in order to shed more light on the mechanism of Ni particle incorporation into the Al metal matrix. We could show that particle incorporation at the beginning of the deposition mainly takes place via particle adsorption at the substrate. As the thickness of the coating increases, it seems that the main mechanism for particle incorporation is via the reduction of Al2Cl7 - ions adsorbed at the particles surface. Three different Ni NPs concentration were tested in this work: 5, 10 and 20 g/L. Although a considerable high incorporation of Ni NPs has been achieved from the IL electrolyte containing the highest concentration of Ni NPs (i.e. ~ 33 wt.% from a 20 g/L of Ni NPs bath), a high concentration of NPs in the ionic liquid resulted having a negative effect in terms of quality of the coatings, due to local cathodic passivation, or solidification of the electrolyte in a poorly conductive compound. This phenomenon has been related to the increase in viscosity originating from the decrease in rotational mobility of the [EMIm]+ cation, as detected by 1H NMR. Despite this fact, almost equivalent amounts of Ni and Al (Ni ~ 45 wt.% and Al ~ 44 wt.%) have been detected by energy-dispersive X-ray spectroscopy mapping in some areas of the coatings prepared with longer pulse off-time (f = 0.05 Hz, t off= 10 s). Such a layer composition would be convenient for the targeted application. Nevertheless, more studies related to the homogeneity of the deposits, as well as ignition tests, must be performed to evaluate the suitability of the coatings to trigger a self-propagating reaction.

A Self-Healing System for Polydicyclopentadiene Thermosets.

Self-healing offers promise for addressing structural failures, increasing lifespan, and improving durability in polymeric materials. Implementing self-healing in thermoset polymers faces significant manufacturing challenges, especially due to the elevated temperature requirements of thermoset processing. To introduce self-healing into structural thermosets, the self-healing system must be thermally stable and compatible with the thermoset chemistry. This article demonstrates a self-healing microcapsule-based system stable to frontal polymerization (FP), a rapid and energy-efficient manufacturing process with a self-propagating exothermic reaction (≈200 °C). A thermally latent Grubbs-type complex bearing two N-heterocyclic carbene ligands addresses limitations in conventional G2-based self-healing approaches. Under FP's elevated temperatures, the catalyst remains dormant until activated by a Cu(I) co-reagent, ensuring efficient polymerization of the dicyclopentadiene (DCPD) upon damage to the polyDCPD matrix. The two-part microcapsule system consists of one capsule containing the thermally latent Grubbs-type catalyst dissolved in the solvent, and another capsule containing a Cu(I) coagent blended with liquid DCPD monomer. Using the same chemistry for both matrix fabrication and healing results in strong interfaces as demonstrated by lap-shear tests. In an optimized system, the self-healing system restores the mechanical properties of the tough polyDCPD thermoset. Self-healing efficiencies greater than 90% via tapered double cantilever beam tests are observed.

Manufacturing multifunctional vascularized composites by through-thickness frontal polymerization and depolymerization: A numerical study on the impact of sacrificial fiber configurations

Concurrent through-thickness frontal polymerization and vascularization (FP-VaSC) is emerging as a promising alternative to conventional multi-step fabrication approaches for vascularized thermoset polymers and composites. This method relies on a localized and self-propagating exothermic polymerization reaction front of the polymer matrix, to simultaneously cure the matrix, and depolymerize pre-embedded sacrificial templates. It delivers fully cured thermoset polymers and composites rapidly and energy-efficiently with the desired vascular system in a single step. While previous studies demonstrated the capability of this method for making woven laminates with a single vascular channel created by embedding a single straight sacrificial fiber, it is desirable to explore the potential of this method for making composites with multiple channels for more practical applications. We employ a previously validated thermo-chemical model from our prior study, to systematically investigate the reaction process with the presence of multiple sacrificial fibers. Two sacrificial fiber configurations are considered, namely, inline and staggered fiber configurations. Within each configuration, we consider a range of horizontal and vertical fiber spacing, which also lead to different sacrificial fiber volume fractions. This study reveals the interactions between the sacrificial fiber and the reactions, identifies the working window of this method for different sacrificial fiber configurations, and provides guidance for manufacturing laminates with multiple vascular channels. We also propose an analytical model that can quickly approximate the maximum sacrificial fiber volume fraction that can lead to successful FP-VaSC for a given carbon fiber volume fraction and compare the results with those from the thermo-chemical modeling.

The research on the application of self-propagating interconnection technology in silicon optical transceiver module for aerospace

PurposeThis paper aims to investigate the bonding of the photonic integrated circuit (PIC) chip with the heat sink using the AlNi self-propagating soldering method.Design/methodology/approachCompared to industrial optical modules, optical modules for aerospace applications require better reliability and stability, which is hard to achieve via the dispensing adhesive process that is used for traditional industrial optical modules. In this paper, 25 µm SAC305 solder foils and the AlNi nanofoil heat source were used to bond the back of the PIC chip with the heat sink. The temperature field and temperature history were analyzed by the finite element analysis (FEA) method. The junction-to-case thermal resistance is 0.0353°C/W and reduced by 85% compared with the UV hybrid epoxy joint.FindingsThe self-propagating reaction ends within 2.82 ms. The maximum temperature in the PIC operating area during the process is 368.5°C. The maximum heating and cooling rates of the solder were 1.39 × 107°C/s and −5.15 × 106°C/s, respectively. The microstructure of SAC305 under self-propagating reaction heating is more refined than the microstructure of SAC305 under reflow. The porosity of the heat sink-SAC305-PIC chip self-propagating joint is only 4.7%. Several metastable phases appear as AuSn3.4 and AgSn3.Originality/valueA new bonding technology was used to form the bonding between the PIC chip with the heat sink for the aerospace optical module. The reliability and thermal resistance of the joint are better than that of the UV hybrid epoxy joint.

Effects of diffusion barriers on reaction wave stability in Co/Al reactive multilayers

Bimetallic, reactive multilayers are uniformly structured materials composed of alternating sputter-deposited layers that may be ignited to produce self-propagating mixing and formation reactions. These nanolaminates are most commonly used as rapid-release heat sources. The specific chemical composition at each metal/metal interface determines the rate of mass transport in a mixing and formation reaction. The inclusion of engineered diffusion barriers at each interface will not only inhibit solid-state mixing but also may impede the self-propagating reactions by introducing instabilities to wavefront morphology. This work examines the effect of adding diffusion barriers on the propagation of reaction waves in Co/Al multilayers. The Co/Al system has been shown to exhibit a reaction propagation instability that is dependent on the bilayer thickness, which allows for the occurrence of unstable modes in otherwise stable designs from the inclusion of diffusion barriers. Based on the known stability criteria in the Co/Al multilayer system, the way in which the inclusion of diffusion barriers changes a multilayer's heat of reaction, thermal conductivity, and material mixing mechanisms can be determined. These factors, in aggregate, lead to changes in the wavefront velocity and stability.

Bonding with brazing alloys as high-temperature interconnection filler through self-propagating exothermic reaction

There has been growing interest in wide bandgap (WBG) semiconductors including SiC and GaN due to the increasing demands for electronic devices serving at high temperatures. However, to maximise the potential capacity of WBG devices, new high-temperature interconnection materials and processes are indispensable as the current existing Sn-based solder alloys and bonding processes developed for Si devices are unable to meet the reliability requirements. In the present work, reactive brazing alloys including Cu-15Ag-5P and Incusil (Ag-27.25Cu-12.5In-1.25Ti) with melting points above 600°C have been utilized as the interconnection materials which offer excellent properties under high operation temperature. The self-propagating exothermic reaction (SPER) was applied for the bonding process via an intense rapid local heating and cooling at a millisecond scale. The strong Cu/Cu-15Ag-5P/Cu and Cu/Incusil/Cu sandwich bonded structures have been created with the assistance of SPER, where the nanofoil was applied from the outside of stacked structures as an external heat source and the bonding process was conducted in the ambient atmosphere without using flux. It has been found that the P element in Cu-15Ag-P alloy has the self-flux effect, which is beneficial for the ultra-fast interfacial reaction process. The experiments where the nanofoil was placed inside of stacked structures between two sheets of brazing alloys have also been conducted, which exhibited the well-bonded interface microstructures between nanofoil and brazing alloys. The outlook on the design for practicality and industrial uses for SPER-assisted bonding with brazing alloys has also been discussed, as a potential viable assembly route for the high-temperature and high-power electronics packaging.

In situ synthesis and regulation of spherical Ti6Al4V powder by calciothermic self-propagating metallurgy

In this paper, spherical Ti6Al4V alloy powder was successfully prepared by calciothermic self-propagating rapid reaction method, in which TiO2, V2O5, Al and Ca were used as raw materials. The reduction reaction can be completed in minutes with no need for any external energy and additives in the reaction process. By investigating the influence of the additives, the amount of reductant Ca added, the reaction pressure and the particle size of Ca, on the composition as well as the morphology of the product, the optimal alloy powder with an low oxygen content of 0.21 wt% was obtained, whose average particle size and specific surface area were 15.28 μm and 0.284 m2/g respectively. Moreover, this research implied the adiabatic temperature of the system and the liquid Ca are the main factors that pose influence to the powder morphology during sintering-reduction-spheroidization-solidification process. Compared with the traditional Ti6Al4V alloy powder preparation process, this process stands out with characteristics of high purity, short production cycle and environmental friendliness, which show high commercialization potential for industrial preparation of Ti6Al4V and similar alloy powders.

Mechano-Activated Self-Immolation of Hydrogels via Signal Amplification.

Cellular organisms possess intricate mechano-adaptive systems that enable them to sense forces and process them with (bio)chemical circuits for functional adaptation. Inspired by such processes, this study introduces a hydrogel system capable of mechanically activated and chemically transduced self-destruction. Our judiciously designed hydrogels can mechanically generate radicals that are processed and amplified in a self-propagating radical de-crosslinking reaction, ultimately leading to mechanically triggered self-immolation. We put such systems to work in mechano-induced debonding, and in a bilayer actuator, where swelling-induced bending generates sufficient force for selective degradation of one layer, leading to autonomous self-regulation associated with unbending. Our work helps define design criteria for molecularly controlled adaptive and self-regulating materials with embodied mechano-chemical information processing, and showcases their potential for adhesives and soft robotics.

Low-temperature joining of alumina ceramic and nickel by Al-Ni self-propagating nanofoil

To meet the requirements of alumina ceramics in delicate electronics, there is an urgent need for a low-temperature bonding technology that can realize a good combination of alumina and metal. In this work, alumina ceramics and nickel metals were successfully connected at a low temperature (25–150 °C) by Al-Ni self-propagating nanofoil as a heat source. The interface microstructure and element distributions of the solder joints from cross-section and fracture surface were investigated. In addition, the solder joint formation process was simulated by finite element analysis and molecular dynamics. These results showed that their shear strengths could be continuously improved with the growing temperature, which were 17.4 MPa (room temperature, 25 °C), 19.5 MPa (50 °C), 22.9 MPa (100 °C) and 25.69 MPa (150 °C). The Al2O3/Al-Ni nanofoil/Ni solder joints were prone to crack at the corner and boundary at Al2O3/solder interfaces due to the stress concentration. Moreover, the increase in ambient temperature not only raises the melting time and transient temperature during the self-propagating reaction, but also improves the interdiffusion of Ni and Sn atoms at the Ni/Sn interfaces.