Phase Composition Research Articles

Kinetics and mechanisms of high-temperature oxidation in BCC and FCC high-alloy Fe-based alloys with high volume fraction of carbides

This study conducts a detailed analysis of high-temperature oxidation and microstructural evolution in two high-alloy Fe-based alloys, each characterized by a high-volume fraction of carbides but differentiated by their matrices − body-centered cubic (BCC) and face-centered cubic (FCC), which was achieved by the addition of nickel. By investigating the intricate interplay of factors such as phase composition, nickel content, and the presence of carbides, this research aims to elucidate the diverse oxidation kinetics and underlying mechanisms specific to each alloy type. Results show that the BCC alloy exhibits slower oxidation kinetics compared to its FCC counterpart, suggesting better performance in high-temperature environments. Moreover, while both alloys develop strong adhesive oxide scales primarily composed of Cr2O3, the FCC alloy experiences more pronounced scale spallation and cracking. A faster progression of decarburization was observed in the BCC alloy. This comprehensive comparison highlights how variations in matrix structure, along with nickel content and carbide behavior, critically influence oxidation kinetics, scale adhesion, and the overall integrity of oxide scales. Understanding these nuanced interactions is crucial for designing high-performance alloys tailored for extreme operating conditions.

Rapid determination of nine preservatives in tobacco flavor by three phase-hollow fiber-liquid phase microextraction-high performance liquid chromatography

Tobacco flavors are extensively utilized in traditional tobacco products, electronic nicotine, heated tobacco products, and snuff. To inhibit fungal growth arising from high moisture content, preservatives such as benzoic acid (BA), sorbic acid (SA), and parabens are often incorporated into tobacco flavors. Nonetheless, consuming preservatives beyond safety thresholds may pose health risks. Therefore, analytical determination of these preservatives is crucial for both quality assurance and consumer protection. For example, BA and SA can induce adverse reactions in susceptible individuals, including asthma, urticaria, metabolic acidosis, and convulsions. Parabens, because of their endocrine activity, are classified as endocrine-disrupting chemicals. Despite extensive research, the concurrent quantification of trace-level hydrophilic (BA and SA) and hydrophobic (methylparaben, ethylparaben, isopropylparaben, propylparaben, butylparaben, isobutylparaben, and benzylparaben) preservatives in tobacco flavors remains challenging. Traditional liquid phase extraction coupled with high performance liquid chromatography (HPLC) often results in high false positive rates and inadequate sensitivity. In contrast, tandem mass spectrometry offers high sensitivity and specificity; however, its widespread application is limited by laborious sample preparation and significant operational costs. Therefore, it is crucial to establish a fast and sensitive sample pretreatment and analysis method for the nine preservatives in tobacco flavors. In this study, a method for the simultaneous determination of the nine preservatives (SA, BA and seven parabens) in tobacco flavor was established based on three phase-hollow fiber-liquid phase microextraction (3P-HF-LPME) technology combined with HPLC. To obtain the optimal pretreatment conditions, extraction solvent type, sample phase pH, acceptor phase pH, sample phase volume, extraction time, and mass fraction of sodium chloride, were examined. Additionally, the HPLC parameters, including UV detection wavelength and mobile phase composition, were refined. The optimal extraction conditions were as follows: dihexyl ether was used as extraction solvent, 15 mL sample solution (pH 4) was used as sample phase, sodium hydroxide aqueous solution (pH 12) was used as acceptor phase, and the extraction was carried out at 800 r/min for 30 min. Chromatographic separation was accomplished using an Agilent Poroshell 120 EC-C18 column (100 mm×3 mm, 2.7 μm) and a mobile phase comprising methanol, 0.02 mol/L ammonium acetate aqueous solution (containing 0.5% acetic acid), and acetonitrile for gradient elution. Under the optimized conditions, the nine target analytes showed good linear relationships in their respective linear ranges, the correlation coefficients (r) were ≥0.9967, limits of detection (LODs) and quantification (LOQs) were 0.02-0.07 mg/kg and 0.08-0.24 mg/kg, respectively. Under two spiked levels, the enrichment factors (EFs) and extraction recoveries (ERs) of the nine target analytes were 30.6-91.1 and 6.1%-18.2%, respectively. The recoveries of the nine target analytes ranged from 82.2% to 115.7% and the relative standard deviations (RSDs) (n=5) were less than 14.5% at low, medium and high levels. The developed method is straightforward, precise, sensitive, and well-suited for the rapid screening of preservatives in tobacco flavor samples.

Development and thermal property analysis of biobased binary composite heat storage materials

Natural aliphatic dibasic acids are a type of bio-based material that shows promising potential as green phase change thermal storage materials due to their favorable thermophysical properties. However, these materials have been found to have issues with subcooling, low thermal conductivity, and poor temperature matching. In this study, three aliphatic dibasic acids, namely adipic acid (AA), sebacic acid (SA), and azelaic acid (ZA), were selected for further investigation. Three biobased eutectic systems, AA-SA (melting point: 118.3 °C), ZA-SA (melting point: 96.2 °C), and AA-ZA (melting point: 98.4 °C), were then prepared based on the calculation of Schrader's equation and experimental screening. The eutectic systems were thoroughly characterized, revealing thermal conductivities ranging from 0.4 to 0.5 W·m−1·K−1, with all systems exhibiting a subcooling of around 20 °C. Based on the principle of optimal overall performance, the AA-SA system was selected for modification. By incorporating Expanded graphite (EG) as a highly thermally conductive additive and nucleating agent, the AA-SA/EG composite phase change material (CPCM) was successfully prepared. This modification effectively reduced the supercooling degree of the bio-based phase change materials (PCM) and significantly improved its thermal conductivity by a factor of four. The resulting AA-SA/EG CPCM demonstrated excellent temperature suitability and has the potential to contribute to the application of bio-based phase change materials in waste heat recovery and solar energy systems. This study provides valuable insights into the development and optimization of bio-based phase change materials, contributing to the sustainable utilization of renewable resources for thermal energy storage applications.

Investigation of the mechanical properties of lead-free Sn-58Bi solder alloy with cobalt addition through flux doping

Purpose This study aims to investigate the effect of incorporating cobalt (Co) into Sn-58Bi alloy on its phase composition, tensile properties, hardness and thermal aging performances. The fracture morphologies of tensile-tested solders are also investigated to correlate the microstructural changes with tensile properties of the solder alloys. Then, the thermal aging performances of the solder alloys are investigated in terms of their intermetallic compound (IMC) layer morphology and thickness. Design/methodology/approach The Sn-58Bi and Sn-58Bi-xCo, where x = 1.0, 1.5 and 2.0 Wt.%, were prepared using the flux doping technique. X-ray diffraction (XRD) is used to study the phase composition of the solder alloys, whereas scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX) are used to investigate the microstructure, fractography and compositions of the solders. Tensile properties such as ultimate tensile strength (UTS), Young’s modulus and elongation are tested using the tensile test, whereas the microhardness value is gained from the micro-Vickers hardness test. The morphology and thickness of the IMC layer at the solder’s joints are investigated by varying the thermally aging duration up to 56 days at 80°C. Findings XRD analysis shows the presence of Co3Sn2 phase and confirms that Co was successfully incorporated via the flux doping technique. The microstructure of all Sn-58Bi-xCo solders did not differ significantly from Sn-58Bi solders. Sn-58Bi-2.0Co solder exhibited optimum properties among all compositions, with the highest UTS (87.89 ± 2.55 MPa) at 0.01 s−1 strain rate and the lowest IMC layer thickness at the interface after being thermally aged for 56 days (3.84 ± 0.67 µm). Originality/value The originality and value of this research lie in its novel exploration of the flux doping technique to introduce minor alloying of Co into Sn-58Bi solder alloys, providing new insights into enhancing the properties and performance of these solders. This new Sn-Bi-Co alloy has the potential to replace lead-containing solder alloy in low-temperature soldering.

High-throughput liquid chromatography-vacuum differential mobility spectrometry-mass spectrometry for the analysis of isomeric drugs of abuse in human urine.

The use of differential mobility spectrometry at low pressure coupled to liquid chromatography-mass spectrometry (LC-vDMS-MS) was investigated for the analysis of 13 drugs of abuse (DoA) including the following: cocaine, ecgonine methyl ester, cocaethylene, benzoylecgonine, norcocaine, tramadol, isomeric pairs of metabolites; O-desmethyl-cis-tramadol and N-desmethyl-cis-tramadol, and cannabinoids: Δ9-tetrahydrocannabinol, Δ9-tetrahydrocannabidiol, 11-hydroxy-Δ9-tetrahydrocannabinol, 11-nor-9carboxy-Δ9-tetrahydrocannabinol, and 11-nor-9carboxy-Δ9-tetrahydrocannabinol glucuronide. Different parameters were optimized for isomeric separation, such as LC mobile phase composition (20%-100% methanol acetonitrile and isopropanol, flow rate: 8-100 μL/min) and DMS separation voltage. Methanol and acetonitrile significantly affected the compensation voltage of the analytes and improved DMS separation. A short trap/elute LC-vDMS-SIM/MS screening method of 1min was developed to quantify 11 drugs of abuse (except THC/CBD), in addition to a 4-min LC-vDMS-SIM/MS method to identify and quantify five cannabinoids including the isomers THC/CBD and three THC metabolites. THC is the principal psychoactive constituent of cannabis and is a controlled substance in comparison to its isomeric counterpart CBD; this highlights the importance and challenges to resolve these isomeric pairs by analytical techniques. The signal responses were linear over a concentration range of 0.005-10μg/mL for the DoA and 1-1000 ng/mL for cannabinoids. The intraday and interday precision were better than 12.2% and accuracy better than 115%. Urine samples from subjects who tested positive for THC and/or cocaine during roadside drug testing were evaluated to assess the performance of the methods LC-vDMS-SIM/MS and LC-MRM/MS. Results show that the developed LC-vDMS-SIM/MS method presents similar performance to LC-MRM/MS with improved sample throughput.

Evaluation of tribo-mechanical measurements and thermal expansion of Cu-based nanocomposites reinforced by high strength hybrid ceramics

It is known that Copper’s (Cu) electrical conductivity makes it a desirable material for use in industry. Due to poor properties such as hardness, thermal expansion, and corrosion resistance, its applications are limited. This manuscript solves these problems while maintaining no breakdown in electrical conductivity. In this study, high-strength ceramics (SiC nanoparticles and graphene nanosheets) were used as reinforcements in the manufacture of Cu-based hybrid nanocomposites using powder metallurgy technique. X-ray diffraction analysis (XRD) was used to investigate phase composition and crystal size of the milled powders. Transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM), respectively examined the microstructure of the prepared powder powders and sintered nanocomposites. Then, various properties of the sintered samples are measured, including physical, electrical and thermal properties and wear resistance. The obtained XRD technique and TEM images showed decreases in the crystal and particle size of milled samples reaching up to 14.08 and 28.30 nm, respectively for the sample contained 8 vol. % SiC + 0.8 vol. % graphene (SG8). A surprising improvement in the mechanical properties of up to 809.15, 341.84 MPa and 336.56 GPa for microhardness, strength and longitudinal modulus for the sample containing the highest reinforcements, achieving an improvement of up to 122, 61.37 and 41 percent compared to the Cu matrix. Moreover, there was a noticeable improvement in the coefficient of thermal expansion (CTE) and wear rate values of the samples by increasing the percentages of hybrid reinforcements in the examined sintered nanocomposite samples. The Sample SG8 recorded the lowest value, decreasing by about 50.2 and 76.5% compared to the SG1 sample. Finally, adding reinforcements to the Cu matrix had a negative effect on the relative density and electrical conductivity, and the lowest values was 92.94% and8.59 × 106 S/m, respectively for the SG sample.

Spray-Flame Synthesis of NASICON-Type Rhombohedral (α) Li1+xYxZr2−x(PO4)3 [x = 0–0.2] Solid Electrolytes

Since solid electrolytes have a broad electrochemical stability window, are exceptionally electrochemically stable against Li metal, and function as a physical separator to prevent dendrite growth, they are at the forefront of alternate possibilities, further increasing the stability and energy density of Li-ion batteries. NASICON-type electrolytes are a promising candidate due to their negligible moisture sensitivity, which results in outstanding stability and a lower probability of Li2CO3 passivity under the ambient atmosphere. However, one of the most promising representatives, Li1+xYxZr2−x(PO4)3 (LYZP), has multiple stable phases with significant variation in their corresponding Li-ion conductivity. In this paper, we have successfully synthesized the highly ionically conductive rhombohedral phase of LYZP via spray-flame synthesis. Two different solvent mixtures (e.g., 2-ethyl hexanoic acid/ethanol, propanol/propanoic acid) were chosen to explore the effect of precursor composition and combustion enthalpy on the phase composition of the nanoparticle. The as-synthesized nanoparticles from spray-flame synthesis consisted of the crystalline tetragonal zirconia (t-ZrO2) phase, while lithium, yttrium, and phosphate were present on the nanoparticles’ surface as amorphous phases. However, a short annealing step (1 h) was sufficient to obtain the NASICON phase. Moreover, we have shown the gradual phase conversion from orthorhombic β phase to rhombohedral α phase as the annealing temperature increased from 700 °C to 1300 °C (complete removal of β phase). In this context, Y3+ doping was also crucial, along with the appropriate solvent mixture and annealing temperature, for obtaining the much-desired rhombohedral α phase. Further, 0.2 at% Y3+ doping was added to the solvent mixture of 2-ethyl hexanoic acid/ethanol, and annealing at 1300 °C for 1 h resulted in a high ionic conductivity of 1.14∙10−5 S cm−1.

Expanded Insights into Martian Mineralogy: Updated Analysis of Gale Crater’s Mineral Composition via CheMin Crystal Chemical Investigations

This study presents mineral composition estimates of rock and sediment samples analyzed with the CheMin X-ray diffraction instrument on board the NASA Mars Science Laboratory rover, Curiosity, in Gale crater, Mars. Mineral composition is estimated using crystal-chemically derived algorithms applied to X-ray diffraction data, specifically unit-cell parameters. The mineral groups characterized include those found in major abundance by the CheMin instrument (i.e., feldspar, olivine, pyroxene, and spinel oxide). In addition to estimating the composition of the major mineral phases observed in Gale crater, we place their compositions in a stratigraphic context and provide a comparison to that of martian meteorites. This work provides expanded insights into the mineralogy and chemistry of the martian surface.

Effect of superstoichiometric amounts of sodium and phosphorus on the phase composition and ionic conductivity of zirconium and sodium silicophosphates (NASICON)

Effect of superstoichiometric amounts of sodium and phosphorus on the phase composition and ionic conductivity of zirconium and sodium silicophosphates (NASICON)

Synergistic enhancement of metal–organic framework-derived hierarchical porous materials towards photothermal conversion and storage properties of phase change materials

The design and synthesis of composite phase change materials that integrate photothermal conversion and latent heat storage have guiding significance for the efficient development and utilisation of solar energy. In this study, taking into consideration the advantages of metal–organic frameworks (MOFs) with adjustable structure and properties, HKUST-1-derived CuO/hierarchical porous carbon materials were employed and integrated with palmitic acid (PA) to synthesise composite phase change materials that exhibit exceptional comprehensive properties. The effects of different carbonation temperatures on HKUST-1-derived CuO/hierarchical porous carbon were analysed through a series of characterisations. The hierarchical porous structure in the blended system offers abundant pore structure and high specific surface area to prevent leakage of phase change materials. Composite phase change materials can maintain good shape stability and excellent thermal energy storage capacity. The thermal storage efficiency and photothermal conversion efficiency are 98.28% and 81.83%, respectively. Meanwhile, the thermal conductivity of the composite phase change material is 3.65 times that of pure PA. In conclusion, the MOFs derivative-based composite phase change materials designed in this study exhibited potential for thermal energy storage and can be applied to the field of solar energy conversion and storage systems.

Laser-directed energy deposition of low-carbon, low-temperature ultra-fine bainitic multi-physical modeling, microstructure and performance studies

An innovative iron-based alloy powder characterized by reduced carbon content and elevated Mn content was developed, leading to the fabrication of iron-based ultrafine bainitic steel with exceptional mechanical properties utilizing laser-directed energy deposition (L-DED). The layers' morphology, microstructure, phase composition, and elemental distribution were analyzed, indicating that the melting depth of the layer was deep and ultra-fine dendrite formed in the top region. A multi-physical powder and melt pool simulation was conducted to analyze the melt flow and pool solidification characteristics, showing that the strong downward flow inside the molten pool caused by the powder impingement increased the melting depth. The cooling rate G × R, where G was the temperature gradient and R was the solidification rate, was higher at the top pool boundary, facilitating the ultra-fine dendrite formation at this location. Following subsequent low-temperature isothermal heat treatment, a refined bainitic microstructure emerged within the deposited layer. The bainitic plates in the 573 K isothermally transformed bainite were interspersed with film-retained austenite (RA). Conversely, the bainitic plates formed at a lower temperature (523 K) exhibited a coalesced morphology stemming from the diminished stability of super-cooled austenite. The bainite plates underwent growth and coalescence, ultimately giving rise to the bainitic microstructure. The 523 K transformed coatings demonstrated superior hardness (509.2 HV), strength (1435 MPa), and elongation (11.5 %) compared to the 573 K transformed coatings (456.5 HV, 1241 MPa, 10.1 %). This research holds significant implications for advancing low-carbon bainitic materials with remarkable comprehensive mechanical properties in additive manufacturing applications.

High temperature oxidation behavior of Mo-Zr alloys in pure oxygen condition

In the current study, alloys of Mo-95Zr, Mo-80Zr, Mo-50Zr, Mo-35Zr, Mo-20Zr and Mo-3Zr (at. %) were prepared to investigate the microstructure and oxidation behaviors of the whole composition range of Mo-Zr as-cast alloys. Laves, (Zr) and/or (Mo) intermetallic phases were presented in the primary dendrite, eutectic or peritectic structures in the prepared alloys. The isothermal oxidation process was accompanied by the formation of multi-layer, consisting of the porous and loose ZrO2 and MoO3, which was individually changed from the (Zr), Laves and (Mo). The specimens were examined using a combination of gravimetry and several surface-analytical techniques, including X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscope and electron microprobe. Phases composition on the microstructure and oxidation behavior, and the sources of internal stress and defects formation in oxide layer on these alloys during oxidation have been discussed.

Synthesis of nitrogen-doped crystalline Ga2O3 thin films via trimethylgallium doped NH3/H2/N2/O2 premixed stagnation flames

This study presents a novel and cost-effective technique for fabricating nitrogen-doped crystalline α-Ga2O3 and β-Ga2O3 thin films under atmospheric pressure conditions through flame synthesis for the first time. We employ metal–organic ammonia (NH3)-assisted flame synthesis (MO-NAFS) in a quasi-one-dimensional trimethylgallium (TMG) doped NH3/H2/N2/O2 flat flame to achieve a one-step deposition of Ga2O3 onto c-plane α-Al2O3 substrates. We found that hydrogen (H2) addition directly impacts the crystallinity of the Ga2O3 thin film. When only NH3 is employed as the fuel, a thin-film single-crystal nitrogen-doped β-Ga2O3 was observed. Blending the NH3 with 5 % of H2 yields a single-crystal nitrogen-doped α-Ga2O3, while a further increase of H2 fraction up to 10 % results in a mixture of both α-Ga2O3 and β-Ga2O3 crystals. Remarkably, the nitrogen doping through MO-NAFS was found to persistently result in an N/O atomic ratio as high as 1.12, as determined by the XPS analysis. This approach paves the way to a simple and scalable means for producing crystalline nitrogen-doped Ga2O3 thin films with potential control of crystal phase composition through parameter adjustments.

Optimization of energy storage and electrocaloric performance in Pb(Zr,Ti)O3 via A-Site La and Bi Co-doping

Lead-based ferroelectrics are one of the most fascinating candidates in the field of state-of-the-art electronic technology. Their intriguing properties are further enriched via the realization of morphotropic phase boundaries. Moreover, the A-site chemical substitution provides insight into the emergence of various exotic phases. Here, we employ co-doping of La3+ and Bi3+ at the A-site of Pb(Zr,Ti)O3 (PZT) ferroelectric to broaden the practical perspective of relaxor systems. Here, we emphasize that the A-site co-doping approach introduces technologically appealing amendments in the well-established temperature composition phase diagram of the PZT system. La3+ and Bi3+ doping favors the evolution of a novel response to thermal and field fluctuations. The maximum values of −ΔS are found to be ∼0.157, 0.118 and 0.176 J (kg·K)−1 for x=0.01, 0.02 and 0.03 , respectively. We employ the electrocaloric characteristics and Arrott plot as probing tools. The observation of a negative electrocaloric effect and the systematic reversal of Arrott lines, followed by a poling effect on the dielectric constant, reveals the emergence of ergodic phase as a novel phase. This further reveals that the Bi doping approach leads to the emergence of exotic characteristics in the chemically modified PZT system. The maximum observed recoverable energy for the composition for x = 0.01 is 0.0479 J cm−3 at a temperature of 388 K.

Understanding and Predicting the Thermodynamic Behavior of Fission Products Encountered Between the (U,Pu)O2 Fuel Pellet and the Cladding: Characterization and Modeling Approaches

AbstractThis study provides a comprehensive investigation of the formation and behavior of a layer enriched in fission products encountered between the (U,Pu)O2 fuel pellet and the cladding, designated as JOG (“Joint Oxyde Gaine” in French). Employing a multifaceted approach that combined thermodynamic calculations, experimental synthesis, and advanced characterization techniques, simulated JOG has been synthetized (without radioactive fission products). Using thermodynamic calculations with the TAF-ID database, the phase compositions in the JOG was assessed for various temperatures, pressures, and oxygen potential conditions, revealing insights into the environmental factors influencing JOG formation. Experimental simulation of the JOG composition, exposed to controlled conditions, confirmed the presence of key compounds such as Cs2MoO4, CsI, and PdTe, as evidenced by SEM, EDS, and XRD analyses. The results of the calculations highlighted notable differences in the nature of the phases constituting the JOG under varying pressure and oxygen potential conditions. At 873 K and oxygen partial pressure of 10–4 bar, Cs2MoO4, Pd–Te, and a gas phase rich in tellurium and CsI were predominant, contrasting with the emergence of liquid phases at 70 bar. This study offered a comprehensive understanding of JOG microstructure, and highlighting the importance of accurate characterization for reactor safety. This information lays the foundations for future studies on the chemical interaction between the JOG and the steel cladding.

Binary transition metal oxide: A novel and efficient catalyst for the synthesis of boron nitride nanotubes

AbstractA novel binary transition metal oxide (NiFe2O4) nanosphere catalyst with a diameter of 500 nm has been synthesized by the hydrothermal reaction, which can efficiently catalyze the formation of hexagonal boron nitride nanotubes (BNNTs) with high‐yield and large aspect ratio. Based on the temperature dependence of the product phase composition and microstructure, combined with results generated using single‐component catalysts, the BNNTs formation process can be summarized as follows: NiFe2O4 reacts with NH3 to generate Fe0.64Ni0.36, which dissolves to form a liquid‐phase Ni‐Fe alloy at high temperatures, where the B component in the precursor and the N atom formed by the decomposition of NH3 diffuse on the surface of the Ni‐Fe alloy; when the concentration of B and N exceed the saturation threshold, hollow BNNTs containing catalyst at the tips are precipitated. The formation process is dominated by a vapor‐liquid‐solid mechanism with tip‐growth mode, where the synergistic catalytic effect of the Ni‐Fe binary system promotes a high yield of large aspect ratio BNNTs.

Modification of cement-based circulating fluidized bed combustion slag: Physical grinding and chemical excitation

This study investigates the effects of physical grinding (ball, impact, and jet milling) and chemical modification (using various dosages of Na2SO4, CaO, triethanolamine (TEA), and their composite modifiers) on CFBCS. The fluidity, flexural strength, compressive strength, and expansion rate of different modification methods were tested. Microstructural and phase composition analyses were conducted using X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, mercury intrusion porosimetry, and thermogravimetry-differential thermogravimetry. The results indicated that impact milling improved mortar fluidity by 2.9 % compared to ball milling, while jet milling reduced it by 5.7 %. Chemical modifications decreased paste fluidity but increased mortar strength and reduced expansion rates. Impact milling and jet milling improved 28-day compressive strength by 13.76 % and 16.01 %, respectively, and reduced the 90-day expansion rate by 0.007 % and 0.012 %, respectively. Composite chemical modification (CM-C) enhanced 28-day compressive strength by 23.88 % and reduced the 90-day expansion rate by 0.019 %. Microscopic analysis shows that modification reduced the pores and pore size of the mortar while increasing the hydration products. After TEA modification, rod-shaped AFt forms a reticulated structure, with C–S–H gel and CH crystals adhering to it. The hydration products of CFBCS mortar formed a network after jet milling, and the addition of composite modifiers resulted in a layered, dense structure.

Evaluation and Design for Magnetic Lens Thermal Management Systems Driven by a Layer of Graphite/Paraffin-Based Composite Phase Change Material

Evaluation and Design for Magnetic Lens Thermal Management Systems Driven by a Layer of Graphite/Paraffin-Based Composite Phase Change Material

Self-Propagating High Temperature Synthesis of Composite Material Based on Zirconium and Chromum Oxide

Ceramic composite materials based on stabilized zirconium oxide were obtained by self-propagating high-temperature synthesis. Yttrium oxide was used as a stabilizing additive. The work studied the effect of the content of yttrium oxide additive on the temperature and combustion rate of the materials studied. Also, based on the results of X-ray phase analysis and scanning electron microscopy, the effect of yttrium oxide on the phase composition and microstructure of the synthesized materials was studied.

Direct Fabrication of 3D Electrodes Based on Graphene and Conducting Polymers for Supercapacitor Applications

AbstractThe development of commercially viable composite conducting polymer electrodes for energy storage is limited by the requirement of multiple and complex fabrication steps, low energy density, and poor cycling stability. In this work, a straightforward, economical, single‐step method is developed for creating densely packed nanostructured PEDOT/graphene composite material demonstrating its application as an electrode for supercapacitors. The electrode achieved the highest mass loading reported so far in the literature for composite vapor phase polymerized PEDOT/rGO using aqueous FeCl3 (25.2 mg cm−2), and displayed an ultrahigh areal capacitance of 4628.3 mF cm−2 at 0.5 mA cm−2. The symmetric two‐electrode setup displayed an energy density of 169.3 µWh cm−2 and a 70% capacitance retention after 70 000 cycles, showcasing its exceptional performance and durability.