Partial Reactions Research Articles

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.

Nanoporous Carbon-Supported Bimetallic (Ni, Cu, and Fe)-Mo Catalysts for Partial Hydrogenation of Biodiesel.

Upgrading biodiesel or hydrogenated fatty acid methyl esters (H-FAMEs) by partial hydrogenation is a second-generation biofuel with high specific fuel characteristics, such as superior cold flow properties, higher oxidative stability, and lower hazardous gas emissions, allowing this biofuel to provide excellent fuel properties, over conventional biodiesel. This study assessed the potential of using nanoporous carbon produced from cattail leaves (CL) as an alternative catalyst support. We synthesized various catalysts including monometallic Mo/NPC, Ni/NPC, Ce/NPC, and Fe/NPC catalysts, as well as bimetallic molybdenum-based catalysts doped with nickel, copper, or iron for the partial hydrogenation of soybean biodiesel. The NPC support demonstrated a surface area (S BET) of approximately 1,323 m2g-1, which greatly increases the catalytic activity through the efficient dispersion of catalyst active sites. The partial hydrogenation reaction of soybean FAME over the MoNi/NPC catalyst obtained the highest catalytic activity with enhanced oxidation stability from 3 to 14 h, and the cloud point and pour point increased from 2 to 13 °C and -1 to 10 °C, respectively. Hence, the selection of catalysts is crucial due to their impact on the feasibility of the process and its economic viability. This article focuses on highlighting the effectiveness of a highly promising catalyst for partial hydrogenation as well as examining the variables that influence the primary reaction pathway.

Selective methanol production via CO2 reduction on Cu2O revealed by micro-kinetic study combined with constant potential model

High efficiency electrocatalysis of greenhouse gas CO2 to liquid fuel methanol attracts great attentions that allows energy transformation from renewable electric energy to storable chemical energy. Catalytically converting CO2 to methanol using green hydrogen is a promising pathway to achieve carbon neutrality. In this work, the catalytic activity and product selectivity of the electrochemical CO2 reduction reaction on Cu2O were studied using a micro-kinetic model based on Marcus charge transfer theory. The constant potential model under the grand-canonical ensemble enables the accurate description of binding energies and ground-state charge transfer upon surface adsorption as a function of electrode potential. Firstly, the potential-dependent activation energies and rate constants of all possible elementary reactions involved in CO2 reduction are calculated. Then, the surface coverage and its derivative can be obtained in a steady-state approximation. Finally, the total reaction rate and partial reaction rate can be deduced, allowing for direct comparison with catalytic activity (current density) and product selectivity (Faradaic efficiency). It is found that CH3OH is the dominant product on the Cu2O(111) surface, while CO is the main product on the Cu2O(110) surface. Based on the derived total and partial reaction rates under the steady-state approximation, it is demonstrated that Cu2O(111) exhibits the highest electrocatalytic activity and methanol selectivity at U = −0.6 V vs. SHE. This research presents a methodology for predicting apparent electrocatalytic performance from microscopic reaction energy calculations, which can be applied to other important electrocatalytic reaction mechanisms and performance predictions.

Photonuclear partial reaction cross sections: Systematic uncertainties and reliability

The well-known significant systematic disagreements between cross sections of partial photoneutron reactions (γ,1n) and (γ, 2n) obtained in various experiments majority of which have been carried out at Livermore (USA) and Saclay (France) were analyzed using the objective physical criteria of data reliability. It was found that experimental data for more than 50 nuclei from 51V to 209Bi in general do not meet those criteria and therefore are more or less unreliable. The experimental-theoretical method based on the Combined PhotoNuclear Reaction Model (CPNRM) was used to evaluate partial reaction cross sections that meet the reliability criteria. It was shown using the analysis in detail of differences between evaluated and experimental cross sections that the major sources of large systematic uncertainties in obtained cross sections are certain shortcomings of experimental neutron multiplicity sorting method have been used for indirect separation of partial reactions. It was shown that the newly evaluated cross sections of partial photoneutron reactions differ significantly (at least noticeably) from the ones obtained using the method of neutron multiplicity sorting but agree with experimental data obtained by alternative methods used for reliable direct separation of partial reactions. The consolidated review of many problems with partial photoneutron reaction experimental data reliability and some ways to solve ones are presented.

Enhancing selectivity through forced dynamic operation with intraparticle diffusion limitations: Ethane oxidative dehydrogenation

During steady state operation (SSO) of industrial fixed-bed reactors diffusion limitations are often present. Well-known impacts include the reduced rate of a positive order reaction and reduced selectivity of the desired intermediate product in a sequential reaction system. This work presents an approach for circumventing diffusion limitations through forced dynamic operation (FDO) of metal oxide catalyzed partial oxidation reactions. Through coupled experiments and modeling, we examine the use of FDO to mitigate selectivity losses of the intermediate product in a parallel-consecutive reaction. With the oxidative dehydrogenation (ODH) of ethane (C2H6) to ethylene (C2H4) over an Al2O3 supported VOx catalyst as the model reaction system, FDO is shown to mitigate undesired C2H4 overoxidation to COx that predominates in steady state diffusion-limited pellets, resulting in C2H4 selectivities that are 15 % (absolute) higher compared to SSO in 2.6 mm catalyst pellets. A kinetic model reveals that FDO beneficially alters the distribution of chemisorbed (O*) and lattice (OL) oxygen, which respectively primarily participate in reactions consuming C2H4 and C2H6. FDO is shown to lead to less detrimental impact of diffusion on the ethylene selectivity and yield compared to SSO. During FDO, generated C2H4 reacts with unselective O*, leaving behind selective OL. The reduced bulk phase O2 in the reductive half cycle leads to accumulation of OL, suppressing C2H4 overoxidation. This effect is amplified via C2H4 trapping in the catalyst pellet. Thus, larger catalyst pellets exhibit selectivities that more rapidly increase with reduction time, inducing higher FDO cycle averages compared to SSO. The findings raise the prospect of applying FDO through feed switching or chemical looping as a way to increase intermediate yield in the class of partial oxidation reactions.

Inhibiting the Formation of Toxic HCN Induced by C3H6 Coexistence and Enhancing C3H6 Resistance of Cu-Zeolite in the NH3-SCR Reaction.

The presence of light hydrocarbons (HCs) in diesel exhaust, specifically C3H6, significantly affects the performance of the state-of-the-art Cu-SSZ-13 zeolite NH3-SCR catalysts. It also leads to the formation of highly toxic HCN, posing risks to the environment and human health. In this work, the highly toxic HCN formation is inhibited, and the C3H6 resistance of Cu-SSZ-13 is improved by secondary metal modification via doping with rare earth/transition metal elements. Upon introduction of C3H6, the activity of Cu-SSZ-13 significantly decreases at medium-high temperatures. This is primarily due to the competitive reaction between C3H6 and NH3, which compete for the NH3 reductant required in the NH3-SCR reaction, resulting in the production of HCN. The unfavorable effect is alleviated on the modified catalysts due to their enhanced oxidation capabilities toward C3H6 and the HCHO intermediate, facilitating the complete oxidation of C3H6 to COx. This inhibits the undesirable partial oxidation reaction between C3H6 and NH3, thereby improving the activity of Cu-SSZ-13 at medium to high temperatures and significantly reducing the formation of highly toxic HCN.

Quantitative localisation of titanium in the framework of titanium silicalite-1 using anomalous X-ray powder diffraction

One of the biggest obstacles to developing better zeolite-based catalysts is the lack of methods for quantitatively locating light heteroatoms on the T-sites in zeolites. Titanium silicalite-1 (TS-1) is a Ti-bearing zeolite-type catalyst commonly used in partial oxidation reactions with H2O2, such as aromatic hydroxylation and olefin epoxidation. The reaction mechanism is controlled by the configuration of titanium sites replacing silicon in the zeolite framework, but these sites remain unknown, hindering a fundamental understanding of the reaction. This study quantitatively determines heteroatoms within the zeolite-type framework using anomalous X-ray powder diffraction (AXRD) and the changes in the titanium X-ray scattering factor near the Ti K-edge (4.96 keV). Two TS-1 samples, each with approximately 2 Ti atoms per unit cell, were examined. Half of the titanium atoms are primarily split between sites T3 and T9, with the remainder dispersed among various T-sites within both MFI-type frameworks. One structure showed significant non-framework titanium in the micropores of a more distorted lattice. In both samples, isolated titanium atoms were more prevalent than dinuclear species, which could only potentially arise at site T9, but with a significant energy penalty and were not detected.

Spectroscopic Characterization of Ti Sites in MWW Zeolite in Presence of Hydrogen Peroxide

AbstractTi‐MWW zeolite is a promising catalyst for partial oxidation reactions. In the present work, a Ti‐MWW sample with high TiO2 loading was synthesized. It was revealed that the Ti insertion in the purely siliceous MWW framework mainly occurs during the post treatment washing with HNO3, when the double structure directing agent synthetic method is used. By exploiting carbon monoxide, acetonitrile, pyridine and ammonia as probe molecules in infrared spectroscopy and diffuse reflectance ultraviolet spectroscopy, the acidic behavior of the Ti sites and the interaction of the Ti sites with hydrogen peroxide (H2O2) were revealed. The Ti Lewis acid sites showed stronger acidity than the one observed in Titanium Silicalite‐1 (TS‐1), with MFI framework. This is coherent with previously reported results, suggesting that a significative fraction of the Ti sites in Ti‐MWW are TiOH(SiO)3 instead of Ti(OSi)4. The Ti‐peroxo and ‐hydroperoxo complexes formed upon H2O2 were shown to be more labile than in TS‐1 and they were shown to be completely reversible upon calcination.

Liquefaction pathway of corn stalk cellulose in the presence of polyhydric alcohols under acid catalysis

In this paper, the experiment of cellulose from corn stalk using 1, 2-propylene glycol (PG) and diethylene glycol (DEG) liquefaction catalyzed by phosphoric acid at atmosphere pressure was carried out. The effect of reaction time on the structural changes of cellulose in the liquefaction process of polyhydric alcohols was investigated, aiming at understanding the mechanism of cellulose liquefaction reaction under the action of acid catalyzed polyhydric alcohols. It was found that the liquefaction yield increased first and then decreased with the extension of reaction time, and reached the highest at 150 min (99.34 %). In the phase of increasing liquefaction yield, cellulose was degraded and translated into glucose, which was then converted into plenty of glycosides with PG/DEG. These glycosides were further converted into low molecular weight (LMW) substances such as hydrocarbons, acids, alcohols, esters, ketones, and ethers. At this time, the biofuel contained 70 %–85 % compounds with carbon number less than 25 and 5 %–10 % compounds with carbon number more than 25. As the prolongation of reaction time (after 150 min), quantities of unstable free radicals formed by cellulose degradation could combine with each other or with hydrogen atoms provided by PG/DEG to produce relatively stable macromolecular substances. That is, the polydispersity (Mw/Mn, abbreviated Ð = 1.28) of the generated biofuel at this stage no longer decreased. However, liquefaction residue produced at 240 min had changed essentially, which was completely different from the liquefaction residue produced in the early stage of liquefaction. In conclusion, this paper revealed the partial reaction process of cellulose by studying the structural changes in the liquefaction process of polyhydric alcohols, which laid a theoretical foundation for exploring the liquefaction mechanism of cellulose.

Tuning Ce-doping La0.7Sr0.3Fe0.9Ni0.1O3-δ internal reforming catalyst to enhanced conversion efficiency and coking tolerance of solid oxide fuel cells fueled by oxygen-bearing low concentration coal mine methane

Solid oxide fuel cells (SOFCs) possess the potential to directly utilize abundant low concentration coal mine methane for power generation, which is crucial for energy conservation and reducing greenhouse gas emissions. Herein, Ce-doped La0.55Ce0.15Sr0.3Fe0.9Ni0.1O3-δ (LCSFN) perovskite is firstly employed as an anode internal reforming catalyst to enhance the electrochemical performance, stability, and resistance against carbon deposition in SOFCs. The results demonstrate that Ni-Fe alloy nanoparticles can be effectively precipitated from LCSFN under reducing atmosphere, thereby significantly promoting the partial oxidation reaction of methane while preventing direct contact between methane and Ni particles for the anode. The anode-supported single cells demonstrated exceptional electrochemical performance using a composite catalytic layer consisting of LCSFN-Ce0.9Gd0.1O2-δ (LCSFN-GDC). At 800℃, the utilization of both H2 and 16 %CH4-1 %O2-N2 resulted in the attainment of maximum power densities (MPD) measuring 881.66 mW·cm−2 and 824.69 mW·cm−2, respectively, with the recorded values for polarization resistance were 0.32 and 1.16 Ω·cm2. Additionally, the single cells equipped with LCSFN-GDC internal reforming catalytic exhibit remarkable resistance to carbon deposition, maintaining stable performance for a duration of 100 h using 16 %CH4-1 %O2-N2. These findings underscore the efficacy of methane catalysts in SOFCs, as it not only enhances power generation efficiency through using internal reforming catalyst but also ensures long-term stability by mitigating carbon-related issues.

Manganese-rhodium nanoparticles: Adsorption on titanium oxide surfaces and catalyst for syngas reactions.

Manganese-rhodium (Mn-Rh) nanoparticles have emerged as a promising candidate for catalytic applications in the production of syngas, a critical precursor for a wide range of industrial processes. This study employs a comprehensive, theoretical, and computational approach to investigate the structural and electronic properties of Mn-Rh nanoparticles, with a specific focus on their interaction with titanium oxide (TiO2) surfaces and their potential as catalysts for syngas reactions. The density functional theory calculations are employed to explore the adsorption behavior of Mn-Rh nanoparticles on TiO2 surfaces. By analyzing the adsorption energies, geometries, and electronic structure at the nanoscale interface, we provide valuable insights into the stability and reactivity of Mn-Rh nanoparticles when immobilized on TiO2 supports. Furthermore, the catalytic performance of Mn-Rh nanoparticles in syngas production is thoroughly examined. Through detailed reaction mechanism studies and kinetic analysis, we elucidate the role of Mn and Rh in promoting syngas generation via carbon dioxide reforming and partial oxidation reactions. The findings demonstrate the potential of Mn-Rh nanoparticles as efficient catalysts for these crucial syngas reactions. This research work not only enhances our understanding of the fundamental properties of Mn-Rh nanoparticles but also highlights their application as catalysts for sustainable and industrially significant syngas production.

Effect of MAX phase Ti2SnC content on microstructure, mechanical properties, and friction behavior of iron-based self-lubricating composites

This work focuses on developing novel iron-based self-lubricating composites reinforced with Ti2SnC MAX phase produced by powder metallurgy. Two amounts of Ti2SnC (5 and 10 vol%) and the addition of 10 vol% graphite were evaluated. The microstructure revealed a partial reaction between the matrix and the Ti2SnC, exhibiting a degree of dissociation in the presence of graphite, leading to the precipitation of carbides. The addition of the MAX phase significantly improved the hardness and compression strength. The dry coefficient of friction was around 0.12 for Fe + 5Ti2SnC + 10Gr, showing a remarkable reduction in wear rate up to 85 % compared to pure iron. The results demonstrate a synergistic effect between the MAX phase and graphite, enhancing tribological performance and wear resistance.

Novel Caputo fractional differential approach and hybrid control scheme for finite‐time synchronization of nonidentical delayed reaction–diffusion neural networks

AbstractThis work focuses on the finite‐time synchronization (F‐TS) for nonidentical delayed neural networks (DNNs) including Caputo fractional partial differential operator and reaction–diffusion terms. A novel F‐TS lemma is proposed by constructing a new Caputo differential inequality. Applying the new lemma and designing two hybrid controllers with time delay and the sign function, the F‐TS criteria on the introduced Caputo reaction–diffusion nonidentical DNNs under the Neumann boundary condition are derived by making use of the Filippov differential inclusion, Green's theorem, and fractional Razumikhin theorem. The conditions are expressed through the algebraic inequality which can greatly decrease the computation in checking the F‐TS performance. Moreover, the validity and correctness of the F‐TS results are illustrated by selecting various orders, spatial positions, and diffusion parameters.

Effect of O2/n-C5H12 Ratio on Oxygenates Production from Plasma N-pentane Partial Oxidation

Objective: Non-thermal plasma is a promising method for producing clean fuels. This work provides a deeper understanding of the impact of O2/n-C5H12 ratio on the partial oxidation of n-pentane from both physical and chemical perspectives. Moreover, this work offers insight into improving fuel combustion efficiency and technical support for the preparation of clean fuels. Methods: An experimental system based on dielectric barrier discharge plasma was established. The discharge characteristics and product generation status of n-pentane partial oxidation were measured by changing the concentration of oxygen and n-pentane to evaluate different O2/n-C5H12 ratios. Results: Research on discharge characteristics showed that the O2/n-C5H12 ratio did not affect the discharge mode, and typical Lissajous shapes were present at different ratios. Changing the O2/n-C5H12 ratio affected the oxygen concentration, average electron energy or electron density, and background temperature. As the O2/n-C5H12 ratio increased, the conversion of the n-pentane partial oxidation reaction increased. However, changing the O2/n-C5H12 ratio did not affect the type of generated products. The oxygenates exhibited a volcano curve, and an O2/n-C5H12 ratio of 1.00 achieved the highest selectivity of 35.1%. As the O2/n-C5H12 ratio continued to increase, the selectivity of oxygenates decreased and the selectivity of CO2 increased. This was potentially due to a shift from partial oxidation toward complete oxidation, which led to the generation of secondary pollutants. Thus, higher O2/n-C5H12 ratios were not conducive to clean fuel production and environmental friendliness. Conclusion: In the partial oxidation of n-pentane, the highest clean fuel production rate was achieved when the O2/n-C5H12 ratio was 1.00. When this ratio exceeded 1.00, the reaction shifted toward complete oxidation, producing secondary pollutants. This study provides ideas for improving fuel combustion efficiency and technical support for the preparation of clean fuels.

P/N synergistic integrated flame retardants with instant cross-linking at high-temperature for flame retardancy and impact resistance of epoxy resins

With the development of flame retardant technology, intumescent flame retardant (IFR) systems, and instant cross-linking in case of fire have become important directions for epoxy resin (EP) flame retardancy. A carbonized matrix containing a benzoxazine structure was constructed with the triazine structure, and the integrated flame retardant (TRBPO) was constructed by introducing the phosphorus source through a partial ring-opening reaction. It can maintain its structural characteristics during the curing process of EP. When EP materials are exposed to fire, TRBPO will cross-link in the EP matrix and work as the P/N synergistic IFR system to achieve excellent flame retardancy. The results showed that 5 wt% of TRBPO could make EP composites reach UL-94 rating of V-0 with a PHRR of 303.7 kW/m2, and the TSP and TSR were reduced by 48.5 % and 48.9 %, respectively, compared with pure EP. The introduction of TRBPO has a impact resistance effect on EP, and its excellent stress dispersion effect made the impact strength of 5-TRBPO/EP reached 36.49 KJ/m2. The analysis of the flame retardant mechanism proved that the rapid carbon formation function of IFR and the self-crosslinking flame retardancy of TRBPO in the fire are the main reasons for flame retardancy. In addition, the capture of flammable groups in the gas phase is an important source of flame retardant effect.

Influence of Nitrogen Loading on the Performance of Partial Nitrification Processes and the Evolution of Microbial Communities

Stable and efficient partial nitrification reaction and nitrite accumulation are essential for the operation of partial nitrification-anaerobic ammonia oxidation process. This paper investigated the changes in the performance of a partial nitrification bioreactor during the domestication process. After 40 days of domestication, the partial nitrification reaction remained stable, the nitrite accumulation rate (NAR) increased significantly to 85.7%, and the NO2 --N/NH4 +-N ratio stabilized at 1.25 ± 0.04. Both diversity indices (Simpson and Shannon) and richness indices (Ace and Chao1) tend to decrease with domestication. Nitrosomonas as a typical ammonia oxidizing bacterium it increased its relative abundance in the reactor from 0.02 ± 0.007% at P1 to 11.6 ± 2.2% at P2, and at P3 stage the denitrifying functional bacteria norank_f_AKYH76, Dokdonella and unclassified_f_Comamonadaceae reached 33.4 ± 12.5%, 18.8 ± 1.8%, and 10.1 ± 1.3%, respectively, and the increase in the relative abundance of these functional species was also consistent with the accumulation of nitrite nitrogen in the reactor.

Catalytic mechanism of calcium ion on the NOx precursors formation during the pyrolysis of kitchen waste

Calcium ion (Ca2+) in kitchen waste exerts a significant impact on the formation of NOx precursors to affect the release of nitrogen oxides during the incineration process. However, the catalytic mechanism of Ca2+ is still unclear. Herein, 2,4-imidazolidinedione is employed as the nitrogen-containing model to study the effect of Ca2+ on the generation of NOx precursors during pyrolysis. Through density functional theory calculations (DFT) and wave function analysis of the catalytic effect of Ca2+, the results indicate that Ca2+ has different degrees of impact on the energy barriers of the initial ring opening reaction. Ca2+ not only changes the rate determining steps of NOx precursors formation pathways, but also reduces the total energy barriers formed by NH3. At the same time, the total energy barriers of all paths formed by HCN are raised. This work theoretically explains the phenomenon of Ca2+ promoting the formation of NH3, whereas inhibiting the release of HCN in pyrolysis experiments. In addition, Ca2+ promotes partial reaction pathways for the formation of HNCO, and the total energy barriers of catalytic pathways are lower than that of the uncatalyzed pathways. Therefore, under the catalysis of Ca2+, the generation pathway of HNCO is more competitive and it is conducive to the formation of HNCO.

Fine grained textured BaTiO3-based piezoelectric ceramics with outstanding strain properties for the lead-free multilayer actuator

Textured BaTiO3-based piezoelectric ceramics show the excellent application potential as their piezoelectric characteristics almost approach the commercial lead-based ceramics. Piezoelectric multilayer actuators (MLAs) with low driving voltages and compact structures are great in line with the equipment trend of miniaturization and functional integration. However, the coarse textured grains result in few grain layers in each thin ceramic layer of MLAs, hardly guaranteeing the electromechanical dependability. In this work, we combined the composition regulation with a modified template grain growth (TGG) to prepare fine-grained textured ceramics. The Zr4+ and Sn4+ co-substituted (Ba0.95Ca0.05)(Ti0.94Zr0.05Sn0.01)O3 (BCZTS) was chosen as the matrix composition. Unreacted BaCO3 (BC, 7.3 % in content) was artificially introduced into matrix to realize the partial reaction template grain growth (RTGG), reducing textured grains from 9.7 μm to 6.9 μm. Textured BCTZS-BC MLAs achieved high texture degree of 92 % and further smaller grain size of 3.4 μm at 1300 °C, due to inhibition on mass transfer and improvement on thermal conductivity of Pt electrodes. The high strain of 0.12 % in textured MLAs is almost 2.3 times enhancement compared to non-textured counterparts, and the ultralow strain hysteresis Hs of 5.6 % at 30 kV/cm is equivalent to that in PZT MLAs. The microscopic coercive voltage is 3.1 V with a maximum displacement of 210 p.m., which is mainly ascribed to the smaller domain sizes and the favorable “4O” domain configuration in textured MLAs.

Partial melting mechanisms of peraluminous felsic magmatism in a collisional orogen: An example from the Khondalite belt, North China craton

AbstractSedimentary‐derived (S‐type) granites are an important product of orogenic metamorphism, and a range of subtypes can be recognized by differences in field occurrence, mineralogy and geochemistry. These subtypes can reflect variations of initial protolith composition, partial melting reactions, pressure and temperature of anatexis, or magmatic processes that occur during ascent through the crust (e.g. mineral fractional crystallization or crustal assimilation). Together, these diverse factors complicate geological interpretation of the history of peraluminous felsic melt fractions in orogenic settings. To assess the influence of these factors, we performed integrated field investigation, petrology, geochemistry, geochronology and phase equilibrium modelling on a series of leucosomes within migmatite associated with different S‐type granites within the Khondalite belt, North China craton (NCC), which is an archetypal collisional orogen. Three types of leucosome are recognized in the east Khondalite belt: leucogranitic leucosome, K‐feldspar (Kfs)‐rich granitic leucosome and garnet (Grt)‐rich granitic leucosome. Phase equilibrium modelling of partial melting and fractional crystallization processes indicate that the leucogranitic leucosomes were mostly produced through fluid‐present melting, Kfs‐rich granitic leucosomes are produced through muscovite dehydration melting with 3 vol.% garnet fractional crystallization, and Grt‐rich granitic leucosomes are produced through biotite dehydration melting with 20–40 vol.% K‐feldspar fractional crystallization and up to 20 vol.% peritectic garnet entrainment. Mineral fractional crystallization and peritectic mineral entrainment occur in the source during melting, and play equally important roles in partial melting mechanisms in terms of affecting the geochemical compositions of granitic melts. Thus, we suggest that peraluminous felsic magmas preserved in collisional orogens are dominantly produced by fluid‐absent melting in the middle to deep continental crust, although extraction of low‐volume melt fractions from an anatectic source region at shallower depths during fluid‐present melting can also generate small amounts of S‐type granites that subsequently crystallize at high structural levels in the crust.

Structural characteristics and mechanical properties of partially reacted and non-reacted Al–Fe66Cr10Nb5B19 metallic glass composites

The microstructure and mechanical properties of partially reacted and non-reacted Al–Fe66Cr10Nb5B19 metallic glass composites obtained by spark plasma sintering were comparatively analyzed. For the first time, the compositional features of core-shell particles formed upon the partial reaction of the Fe66Cr10Nb5B19 metallic glass with aluminum were examined using transmission electron microscopy combined with elemental mapping. The key finding is that iron of the alloy selectively dissolved in aluminum. The inner layer of the shell formed via diffusion of aluminum into the metallic glass. The introduction of the glassy reinforcement did not lead to such a dramatic ductility reduction as the formation of a complex “metallic glass core-thick intermetallic shell” reinforcement. In the non-reacted composite, the glassy reinforcement did not reveal its full potential in terms of the strengthening effect.