Powder Mixtures Research Articles

In situ phase engineering during additive manufacturing enables high-performance soft-magnetic medium-entropy alloys.

Additive manufacturing (AM) shows promise as a method for producing soft-magnetic multicomponent alloys for use in electric motors and sustainable electromobility applications. However, the simultaneous achievement of a high saturation magnetic flux density (Bs) and a low coercivity (Hc) in AM soft-magnetic materials remains challenging. Herein, we present an approach that integrates an elemental powder mixture of Fe45Co30Ni25 with Fe2O3 nano-oxides, which is then subjected to laser powder bed fusion (LPBF) followed by high-temperature annealing to achieve an FCC-structured Fe45Co30Ni25 MEA/FeO composite. The FeO nanoparticles, a byproduct of the reaction between Fe powders and Fe2O3 nano-oxides, serve as nucleation sites for the formation of a single FCC phase in the MEA matrix. The resulting LPBF MEA/FeO composite has a Bs of 2.05 T and an exceedingly low Hc of 115 A m-1, compared to those of the BCC/FCC dual phase MEA and other state-of-the-art additively manufactured soft-magnetic alloys. In situ Lorentz transmission electron microscope (TEM) revealed that the low Hc of the FCC-structured MEA/FeO composite originates from the reduced pinning effect of grain boundaries in the FCC phase on domain wall movement compared with those in the FCC/BCC dual phase.

Synthesis of ZrW2O8–ZrC composite powders by solid‐state exothermic oxidation reaction of ZrC and WO3 powders

AbstractIn this work, ZrW2O8‐coated ZrC composite powders are synthesized by solid‐state reaction method using ZrC and WO3 powders. Thermodynamic analysis shows that when the molar ratio of ZrC to WO3 is larger than 5:4, ZrW2O8 cannot be synthesized by solid reaction of ZrC and WO3. The favorable molar ratio of ZrC to WO3 for solid reaction synthesis ZrW2O8 is 1:2. After reacted below 800°C for 8 hours, only ZrC in the ZrC and WO3 mixture powders partially reacts with oxygen to form ZrO2. And there is no detectable reaction between WO3 and the formed ZrO2 to produce ZrW2O8. ZrC and WO3 can synthesize ZrW2O8 at 900°C. ZrW2O8‐coated ZrC composite powders can be synthesized using powder mixtures with molar ratio of ZrC:WO3 = 1:1.7 and ZrC:WO3 = 1:1.9 after heat treatment at 1000°C for 4 hours. The synthesized ZrW2O8‐coated ZrC particles show cubic shape with obvious particles growth. The exothermic oxidation reaction of ZrC leads to a significant increase in local temperature, which is believed to trigger partial reaction between ZrO2 and WO3 to form ZrW2O8.

Enhancing magnesium oxalate cements with copper slag and silica fume

Magnesium oxalate cement is an alternative binder made by reacting dead-burned magnesia and oxalic acid salts. Dead-burned magnesia, which has a high carbon footprint, was replaced at different levels (25–100 %) with copper slag, as a source of iron and thus a reactive component, or silica fume, as an inert or low-reactivity component. The powder mixtures contained ∼25–35 % oxalate, by mass. Physical and mechanical properties were investigated as well as changes in the mineralogy and morphology of paste and mortar specimens. Replacement of up to 50 % of dead-burned magnesia yielded strong (> 30 MPa) and water-resistant mortars with extended setting times, for mixtures with lower oxalate content. Mixtures with higher oxalate content and those without any dead-burned magnesia suffered significant strength loss in water. When copper slag was used, humboldtine, an iron oxalate, formed instead of or in addition to glushinskite, the main reaction product of magnesium and oxalate ions. Silica fume did not yield any crystalline reaction products.

Characteristics of powder charging behavior via forced triboelectric charging on an inclined chute

This study presents a novel method for selective charging of powders by dry triboelectric forced charging utilized as the first stage of material sorting in an electric field. In forced triboelectric charging, a high voltage is applied to the copper chute in which particles are charged during their transportation. In this research, the effect of the operating parameters of the chute, including mass flow rate, angle of inclination, and length, on the specific particle charge of limestone powders was investigated. In addition, the behavior of the charged particles in an electrostatic sorter was analyzed by evaluating their charge distribution after sorting. The results reveal that as the length of the chute increases, the specific charge asymptotically approaches a saturation value, which is determined by the high voltage applied. Furthermore, for a given chute length, the high voltage influences the amount and the sign of the specific particle charge, including a high voltage value at which the particles are neutral on average, i.e. the so-called point of zero net charge (PZNC). This PZNC is of particular interest for sorting out a target component from a powder mixture. However, if the mass flow rate is increased above a certain value, the specific charge decreases as the number of particle wall contacts is reduced due to stratification. Bipolar charge distributions were observed for all investigated high voltages, with the distribution width increasing with particle size to the power of 2.1. The modal value of the charge distribution shifts according to the difference in voltage applied to the PZNC.

A room temperature chemical process for homogeneous mixing of precursor phases for low temperature tetracalcium phoshate preparation

The aim of this study was to prepare phase pure tetracalcium phosphate (TTCP) from the precursor phase mixtures homogeneous at the nano/microscale level at lower heat treatment temperatures in much shorter dwell times.Two different precursor powder mixtures were prepared by reacting CaCO3 with H3PO4 in ethanol or water. The resultant precursor powder mixtures were heat treated at temperatures in the 1200–1350 °C range for 2 and 5 h. Phase structures of the powders were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) and Raman spectroscopy analysis. Scanning electron microscopy (SEM) was used for the investigation of powder particle sizes and morphology. Powders synthesized by the heat treatment of both of the starting powder mixtures prepared in ethanol or water with 2 and 5 h of dwell times at 1350 °C were determined to be phase pure TTCP. SEM analysis along with the phase identification showed that the precursor powder prepared in ethanol had micron sized plates formed by aggregation of sub-micron sized thin CaHPO4 plates covering CaCO3 particles. The precursor powder prepared in water contained large aggregates of sub-micron sized CaCO3 particles whose surface was covered by precipitated nano-sized hydroxyapatite. TTCP powders were composed of large irregularly shaped particles formed by sintering of smaller equiaxed grains. Average grain and particles sizes of the TTCP powders synthesized from the precursor powder prepared in ethanol were 3.2–3.9 and 8.1–8.4 μm, respectively. Average grain and particle sizes of the TTCP powders synthesized from the precursor powder prepared in water however were measured to be 3.3–5.1 and 11.2–11.6 μm, respectively.The TTCP preparation method presented in this study provides homogeneous and well-mixed precursor powders prepared from cheap and commonly available precursors without milling and decreases the heat treatment time to 2 h at 1350 °C.

Multi-functional polysaccharides composite film containing cashew and jik leaf carbon dots: Properties and bioactivities

Carbon dots (CDs) from the leaf powders of cashew (C-CDs), jik (J-CDs) and the mixed cashew/jik (1:1) (CJ-CDs) using hydrothermal method were synthesized and characterized. All three CDs were incorporated into chitosan/starch composite (CS) film at the level of 3 % (w/w). Microstructure images revealed that all films had slight differences in surface and internal structure. Thickness of the CS film increased with the inclusion of fillers (CDs). Inclusion of CDs slightly reduced the tensile and water vapor barrier properties of the CS film. CS film containing C-CDs exhibited the improved elasticity, UV barrier and antioxidant activity among all the films tested. Color and opaqueness of the resulting films were governed by the yellowish CDs. Distinctive peaks of resulting CS film were detected in FTIR spectra, while all CDs had no marked effect on the spectra. The release of CDs from films was more pronounced in water than in alcoholic solutions (10–95 % ethanol). Strongest antibacterial activities against Listeria monocytogenes and Escherichia coli were recorded for CDs added film, in which the highest activities were found for CS/CJ-CDs film. Thermal stability was also enhanced in CS/CJ-CDs film. Thus, the CS film loaded with CDs, especially from the mixture of cashew and jik leaf powders could serve as a promising active packaging for inactivation of some pathogens in food products.

Alkaline activation via in-situ caustification of one-part binders of composite precursors of waste glass and limestone

Mixtures of powders of waste glass (WG), limestone (LS), Na2CO3 and CaO were used to formulate novel one-part in situ alkali-activated cement (WG-AAC). The in-situ interaction Na2CO3-CaO-H2O promoted the formation of CaCO3 and NaOH, which promoted the WG and LS dissolution and influenced the micro- and molecular features of the resulting cementitious products. Pastes and mortars developed 1-year strengths of up to 29 MPa and were stable underwater. Characterization by XRD, SEM, EDS, and 29Si-NMR indicated that a Na2CO3:CaO ratio close to 1:1 resulted in polymerized C-S-H, CaCO3, silica gel, and Ca-modified silica gel, which were intimately intermixed and possibly crosslinked through Q3 bonds. Such phases interacted synergistically improving the underwater stability of the WG-AAC, indicating that in-situ caustification is a suitable and practical alkaline activation for SiO2-rich precursors.

Accelerating pharmaceutical tablet development by transfer of powder compaction equipment across types and scales

Roller compaction is a key unit operation in a dry granulation line for pharmaceutical tablet manufacturing. During product development, one would like to find the roller compactor (RC) settings that are required to achieve a desired ribbon solid fraction. These settings can be determined from the compression profile of the powder mixture being compacted and a mathematical model that interprets it. However, establishing compression profiles in an RC requires relatively large amounts of powder, which are expensive and may not be available during drug development. As a cost-effective alternative to an RC, a compactor simulator (CS) can be used, which is a small-scale equipment that uses minimal amounts of powder to build the compression profile. However, since the working principles of a CS and an RC are different, the compression profiles obtained from the two devices for a given powder are also different. In this study, we propose a transfer learning approach that allows the RC compression profile of a given powder to be easily predicted from the compression profile obtained in a CS for the same powder. Based on the well-known Johanson model and on the mass correction factor theory, we examine the compaction behavior of six formulations, two of which including active ingredients, and we find that the mass correction factor does not depend significantly on the powder being compacted. We develop a simple, generalized correlation (transfer model) that allows the mass correction factor to be predicted solely as a function of the pressure at which the compaction is carried out. By using the proposed transfer model, the prediction of the RC compression profiles for the validation powders is significantly improved over the case where a constant value of the mass correction factor is used.

Detection of Organic Explosive Residues from Outdoor Detonations using Confocal Raman Microscopy

The detection of post-blast residues in the aftermath of an explosion involving organic explosives with spectroscopic techniques is challenging as, typically, no microscopically visible unreacted particles remain after the explosion. However, some low-order explosions may leave visible particles behind, as well as the presence of significant amounts of unreacted material. In this study, four authentic open-air detonations using two simulated improvised explosive devices (IEDs) containing a mixture of military explosives (TNT and RDX), and two IEDs containing smokeless powder were conducted. The various materials they contained, including plastic, wood, and metal, were swabbed and extracted with acetone to create post-blast liquid extracts. The extracts were then dried and examined using confocal Raman microscopy, alongside a 50 ppm reference mixture of smokeless powder constituents, which was created to evaluate the effects of Raman scattering within the full smokeless powder mixture. Smokeless powder constituents, such as ethyl centralite, diphenylamine, nitroglycerin, and dibutyl phthalate, were successfully identified by comparison to the reference mixture on most substrates, with the exception of the paint stick (wood) substrate. TNT/RDX was also able to be identified in the extracts, with RDX crystals being observed in some dried extracts after solvent evaporation. However, the detection of TNT/RDX in the second detonation was unsuccessful, possibly due to an explosive chain reaction that was highly efficient. No trends were seen in substrate affinity for TNT/RDX. The challenges and benefits with the developed methodology for the detection of organic explosive residues from a variety of substrates are discussed in detail.

Bioconversion of insect protein biomass into a fishmeal alternate for freshwater fish, Oreochromis mossambicus (Peters, 1852) diets

Abstract The demand for alternative fishmeal has increased significantly in recent years due to the expansion of the fishing industry. Therefore, insect proteins are becoming more popular as an alternative low-cost bio-source for fish than plant-based fish feeds. In the present study, a dietary mixture of insect protein powder derived from four Indian grasshopper species, namely Oxya hyla hyla, Atractomorpha crenulata, Oxya japonica japonica, and Phlaeoba infumata (insect meal, IM) was substituted for conventionally used fishmeal (FM) in the diet formulation for growing Mozambique tilapia, Oreochromis mossambicus (Peters, 1852) fingerlings. Three formulated diets with IM were prepared, with FM substituted at the rates of 25%, 50%, and 75%, respectively, with a control diet with no IM but only 20% FM. All dietary treatments were administered to tilapia fingerlings for 60 days under laboratory conditions. IM-incorporated diets outperform FM-incorporated diets in growth and digestibility due to their higher food conversion ratio for IM. In terms of growth and survivability in tilapia fingerlings, a 75% replacement of FM with IM demonstrated the most significant efficacy. According to the findings, mixed insect powder derived from four grasshopper species can be used as a partial replacement for FM in formulating the compound fish diet for tilapia fingerlings.

Hybrid additive manufacturing of ceramic/aluminum-titanium gradient composites via arc and laser cladding eutectic pools

ABSTRACT There is a great deal of interest in improving the efficiency of arc-directed energy deposition (Arc-DED) of aluminium matrix composites and the uniform introduction of reinforcing particles. In this work, ceramic/aluminum-titanium gradient composites were manufactured by hybrid additive manufacturing with arc and laser cladding eutectic pools. The results show that the laser cladding powder feed method can have a higher powder capture rate compared to bypass feeding. Coupling the laser and powder changed the pulsed base-arc characteristics and increased the peak arc length. After the addition of the powder mixture, the aluminium matrix formed an Al3Ti reinforced phase, which evolved from needles to rods as the amount of powder increased. As the content of ceramic particles and the Al3Ti phase increased, the average hardness of the AMC components increased from 55.5–126 HV0.1 and the wear rate decreased from 6.16 × 10−3–1.25 × 10.−3 mm3·N−1·m−1.

3D model of a stable triangle LiF–NaBr–KBr four-component reciprocal system Li+, Na+, K+ || F-, Вr-

A 3D model of the phase equilibrium states of the quasi-three-component system LiF–NaBr–KBr, which is a stable triangle of the four-component reciprocal system Li+, Na+, K+ || F-, Br-, has been constructed. Based on the 3D-model, polythermal, isothermal sections and the polytherm of phase crystallization were constructed for the first time. Two polythermal sections contain wide areas of boundary solid solutions based on sodium and potassium bromide. In an isothermal section at 650 оC, the fields of the liquid phase and the coexisting two and three phases are delimited. The crystallization polytherm is represented by three fields. In the crystallization field of lithium fluoride, the area of separation of two liquids is limited. The direction of the ion exchange reaction 2LiBr + NaF + KF = 2LiF + NaBr + KBr was confirmed by thermodynamic calculations at temperatures of 400, 600, 800, 1000K. The exothermic nature of the exchange reaction is confirmed by taking a DTA heating curve for a mixture of powders from 50% LiBr + 25% NaF + 25% KF, and the phase composition of the reaction products LiF + NaBr(OTR) + KBr(OTR) is confirmed by X-ray phase analysis data, where OTR is limited solid solution.

Magnesium-Titanium Alloys: A Promising Solution for Biodegradable Biomedical Implants.

Magnesium (Mg) has attracted considerable attention as a biodegradable material for medical implants owing to its excellent biocompatibility, mitigating long-term toxicity and stress shielding. Nevertheless, challenges arise from its rapid degradation and low corrosion resistance under physiological conditions. To overcome these challenges, titanium (biocompatibility and corrosion resistance) has been integrated into Mg. The incorporation of titanium significantly improves mechanical and corrosion resistance properties, thereby enhancing performance in biological settings. Mg-Ti alloys are produced through mechanical alloying and spark plasma sintering (SPS). The SPS technique transforms powder mixtures into bulk materials while preserving structural integrity, resulting in enhanced corrosion resistance, particularly Mg80-Ti20 alloy in simulated body fluids. Moreover, Mg-Ti alloy revealed no more toxicity when assessed on pre-osteoblastic cells. Furthermore, the ability of Mg-Ti-based alloy to create composites with polymers such as PLGA (polylactic-co-glycolic acid) widen their biomedical applications by regulating degradation and ensuring pH stability. These alloys promote temporary orthopaedic implants, offering initial load-bearing capacity during the healing process of fractures without requiring a second surgery for removal. To address scalability constraints, further research is necessary to investigate additional consolidation methods beyond SPS. It is essential to evaluate the relationship between corrosion and mechanical loading to confirm their adequacy in physiological environments. This review article highlights the importance of mechanical characterization and corrosion evaluation of Mg-Ti alloys, reinforcing their applicability in fracture fixation and various biomedical implants.

Influence of the Y3Al5O12 on the structure formation and properties of ceramics of the Al2O3 – Y2O3 system

The paper presents results of the study of the structure and physico-mechanical properties of ceramics composits α-Al2O3 + n Y2O3 (n = 0; 0.5; 1; 1.5; 2; 3; 4; 5 wt.%) based on the basis of polymorphic modifications γ+θ-Al2O3 depending on the concentration of the Y2O3 doping impurity and the annealing temperature of the powder mixtures (800 and 900°C). The effect of mutual protection against crystallization was discovered, which results in mutual inhibition of crystallization processes in Al2O3–Y2O3 powder systems. By X-ray diffraction analysis, the formation of a phase of yttrium-aluminum garnet Y3Al5O12 (YAG) in ceramics has been established. The dependence of the mechanical characteristics of the materials under study on the amount and size of the formed phase YAG has been revealed.

Binder Jetting Additive Manufacturing of Inconel 718/TiC Metal Matrix Composites: Influence of TiC Content on Processing, Microstructure, Mechanical and Tribological Properties.

This paper investigated the influence of titanium carbide (TiC) content on the processing, microstructure, mechanical and tribological properties of Inconel 718/TiC composites produced by binder jetting additive manufacturing. It was found that increasing the amount of TiC required an increase of the drying intensity during printing due to a decrease in the thermal conductivity of the powder mixture. The sintering process also depended on the TiC content. The most optimal modes were 1270 °C for 10 h for samples with 0 and 3% TiC and 1280 °C for 5 h for samples with 5 and 10% TiC. The hardness of the materials increased as the proportion of reinforcement increased. The best tensile properties, also at high temperatures, were possessed by samples with 3% TiC, showing high strength and, in addition, satisfactory plasticity. The maximum wear resistance was achieved by the composite material containing 5% TiC.

Characterization of hot‐pressed ZrC–TiC composites

AbstractSynthesis and consolidation of (Zr,Ti)C were investigated in the present work. ZrC–TiC powder mixture was synthesized at 1650°C for 90 min by the carbothermal method. The prepared powder mixture was hot‐pressed at 1800 C for 60 min under a pressure of 40Mpa and then heat‐treated at 2100 C for 60 min. There were ZrC‐rich and TiC‐rich phases together with zirconium oxide phases in powder mixture and hot‐pressed samples, while there were no oxide phases in the heat‐treated sample and only ZrC‐rich and TiC‐rich phases were present in the sample. The FESEM image of the fracture surface of the samples shows that the porosity of the samples decreases with increasing temperature. Relative density, microhardness, and flexural strength increased from 93.8% to 98.6%, from 15.26 to 21.41 GPa, and from 185.02 to 220.69 MPa, respectively, with increasing temperatures from 1800 C to 2100 C. In contrast to these properties, the fracture toughness of the samples was reduced from 3.71 to 3.47 MPa·m1/2. The investigation of oxidation behavior also showed that oxidation is influenced by oxygen diffusion and exhibits nonlinear behavior as a function of time. With increasing oxidation temperature of hot‐pressed and heat‐treated samples from 600 to 1000°C, parabolic oxidation rate constants (kp) increased from .267 to 11.793 and from .367 to 10.993, respectively.

Synthesis of Mo-Cu nanocomposite powder by hydrogen reduction of copper nitrate coated MoO3 powder mixture

The fabrication of Mo-based nanocomposite powder with homogeneous dispersion of Cu was investigated. The fine MoO3 powders were prepared by high energy ball milling, and Cu particles on the ball-milled powder surfaces were formed by calcination of a precursor solution copper nitrate. In the powder mixture calcined at 300 °C, MoO3 and CuO appeared in the form of aggregates with fine particles. Microstructural analysis showed that the oxide powders were changed to Mo-Cu nanocomposite powders with an average particle size of about 150 nm and had microstructural homogeneity by hydrogen reduction at 800 °C for 1 h. These results are help to optimize the synthesis process of homogeneous Mo-Co nanocomposite powders.

Modeling Kinetics and Transport Mechanism Study of Poorly Soluble Drug Formulation in High Acidic Medium

Some medicinal particles are poorly soluble in highly acidic solutions, particularly those subjected to various production processes. Therefore, the present research investigated the kinetics and mechanisms of the drug release rate of newly formulated solid pills in a low pH medium. Three pills were prepared: one from a non-moisturized powder mixture (PILD) and the other two, PILC and PILM, from the dried powder mixtures, which were dried using hot-air heating and microwave radiation, respectively. These pills were subjected to drug release tests, and the outcomes were considered in the kinetics investigation using various models. Zero-order, Hixson–Crowell, First-order, Higuchi, Hopfenberg, Korsmeyer-Peppas, Logistic, and Peppas-Sahlin were the kinetic models used to inspect the release rate mechanism of these tablets. It was found that the Peppas-Sahlin and zero-order were the most reliable models to represent the drug release profile of all prepared pills with very high accuracy, estimated by R^2>0.99. The Hixon and first-order models were the weakest to characterize this work outcome. This work also applied these models to describe the controlling mechanism of the drug release for each prepared pill. It is detected that the non-Fickian diffusion and polymer chain relaxation control the PILC’s release behavior. However, case II transport and super case II transport with erosions is the dominant mechanism for PILD and PILM pills, respectively. Additionally, new semi-empirical models were modified to describe the kinetics of the solid release of those tablets with greater accuracy.

Penetration of Intracoronal Bleaching Agents Across a Calcium Silicate-Based Coronal Barrier in Pulpless Immature Permanent Teeth: An In Vitro Study.

Tooth bleaching procedures on nonvital teeth have been performed for crown discoloration caused by regenerative endodontic therapy (RET). However, leakage of bleaching agents across the root canal can be detrimental. This study aimed to assess and compare the penetration levels of hydrogen peroxide (HP) from different bleaching agents across calcium silicate-based coronal barriers in immature permanent teeth. Fifty extracted single-rooted human teeth were randomly divided into four groups (n = 10): Group I (HH)-35% hydrogen peroxide (HP); Group II (SS)-a mixture of sodium perborate (SP) powder and saline; Group III (SH)-a mixture of SP powder and 30% HP liquid; Group IV (CP)-10% carbamide peroxide gel. The control group (Group V, CC) was treated with distilled water. The bleaching agent was replaced on the 4th day, and penetration analysis was performed on the 7th day using ferro thiocyanate (FTC) method and a UV-spectrophotometer at a wavelength of 480 nm. Compared with the control group, the SH group (SP mixed with HP) showed a significant difference, indicating substantial HP penetration across the root canal space (p value < 0.0001). Intergroup comparisons also revealed a significant difference between the SS and SH groups (p value < 0.0001), suggesting that the SS group had less penetration. Compared with other bleaching agents, SP mixed with saline/water resulted in the lowest HP penetration in the pulp canals of the RET-simulated tooth models. This study is the first to investigate HP penetration from different bleaching agents in teeth that have undergone RET, identifying the safest bleaching agent for use in these cases. This study also provides a foundation for further research to develop precise guidelines for nonvital tooth bleaching protocols in RET-treated teeth.

Study of patterns and mechanisms of combustion of powdered and granulated T-C-B system

Experimental studies of the combustion patterns of the ternary system (100 – x)(Ti + C) – x(Ti + 2B) of bulk density in powder and granular form used for the synthesis of composite ceramics TiC–TiB2 were carried out. The study shows that the dependence of the powder mixture combustion rate on the Ti + 2B content has a non-monotonic character, which is associated with the influence of impurity gas release on the combustion process. By removing the influence of impurity gas by granulation, a monotonic dependence with two characteristic sections was obtained. For the granulated mixture, an increase in the Ti + 2B content 60 wt. % leads to a change from the conductive combustion mode to the convective one, accompanied by a sharp increase in the combustion rate. For the conductive combustion mode, the combustion rate of the substance inside the granule and the combustion transfer time from the granule to the granule were determined, which allowed us to estimate the inhibitory effect of impurity gas release on the combustion rate of powder mixtures of different composition. For the convective combustion mode, it was shown that a decrease in the content of the gasifying additive in the mixture (granulation with ethyl alcohol) led to an unexpected result: an increase in the combustion rate of the mixture. For compositions with (Ti + 2B) 60 wt. % the combustion rate with counter filtration of impurity gases was determined for the first time, which made it possible to estimate the front rate increase according to the filtration combustion theory. According to XRD results, the combustion products of all compositions contain only two main phases TiC and TiB2.