Degree Of Graphitization Research Articles

A comprehensive investigation of thermal coke formation during rapid non-catalytic pyrolysis of rubber seed oil

Due to coking deposits, catalyst deactivation severely affects the upgrading of triglyceride biomass. Understanding the chemical nature and development of coke species is essential for mitigating the degree of coking and for the regeneration process of the catalysts. In this study, SEM, XRD, FT-IR, Raman and XPS are employed to gain insights into the coking behavior of RSO during the rapid pyrolysis process. The results show that pyrolysis of RSO produces high quality syngas with 98.72 % H2 and CO. The unstable O-containing functional groups in the cokes continue to be lost, which indirectly promotes the condensation reaction of aromatic hydrocarbons. The hydroxyl group is the main functional group that affects the reactivity of cokes, and it is one of its more active groups. Although the crystal size of the cokes is growing, its degree of graphitization is decreasing with the temperature increases. The size of the aromatic ring system in the cokes gradually increases with increasing temperature. The cross-linking structure in the coke is constantly being destroyed. Resulting in some O-containing functional groups entering the cokes. Based on this work, the coke evolutionary route of rapid pyrolysis of RSO is proposed.

Effect of Carbon Support on the Properties of Fe, N, S Co-Doped ORR Catalysts Prepared by Molten Salt Method

In recent years, the development of sustainable and environmentally friendly catalysts for various electrochemical processes has become a major focus in the fields of energy storage and fine chemicals. Efficient and cost-effective oxygen reduction reaction (ORR) catalysts are crucial for the advancement of fuel cells and metal-air batteries. This study explores the use of rice husk-based porous carbon (RHPC) with a hierarchically porous structure as a support material for sustainable ORR catalysts. The performance of RHPC was compared with other commercial carbon materials, such as acetylene black (AB) and coconut shell carbon (YP-50), evaluating key properties including particle size, specific surface area, oxygen-containing functional groups, degree of graphitization, and hydrophilicity/hydrophobicity. Compared to AB, which has higher conductivity, and YP-50, which has a greater abundance of oxygen functional groups, RHPC demonstrated significant advantages as a catalyst support. The resulting Fe-NS/RHPC catalyst exhibited high activity (E1/2 = 0.858 V vs RHE, J = 4.83 mA cm−2), outperforming the standard Pt/C (E1/2 = 0.844 V vs RHE, J = 4.99 mA cm−2). When tested in a liquid Zn-air battery, the Fe-NS/RHPC catalyst achieved a peak power density of 116.2 mW cm−2 and a capacity of up to 792.5 mAh g−1.

Microstructural transformation impact on mechanical and tribological performance of different temperature heat-treated carbon/carbon composites

Due to the harsher application environments of C/C composites, optimizing the internal structure of C/C materials through high-temperature treatments (HTT), specifically above 2300 °C, has become an effective method to enhance their properties. The current study investigates the influence of microstructural evolution on the mechanical and tribological behavior of carbon/carbon composites after heat treatments at 2300 °C and 2700 °C. The C/C composites experience a reduction in mechanical properties as the heat treatment temperature is raised. This may be due to the rearrangement of carbon atomic layers at high temperatures, resulting in increased orientation in pyrolytic carbon. However, fibers parallel to the friction surface are relatively less affected, while fibers perpendicular to the friction surface and PyC are more significantly affected. The average coefficient of friction increases from 0.19 to 0.42 as heat treatment temperature from 2300 °C to 2700 °C under the brake pressure of 1 MPa with 25 m/s brake speeds. This phenomenon is attributed to the samples with high graphitization degree (2700 °C) producing a large number of flaky chips under shear stress during friction, which can be easily ground and compacted to form a complete friction film. Additionally, the more easily deformable z-axis fiber asperities increase the contact area, resulting in an increase in the coefficient of friction and friction stability.

Significant Improvement in Thermoelectric Properties of Carbon-Reinforced Cementitious Composites Achieved by Regulating the Graphitization Degree of Expanded Graphite.

Building structures are exposed to direct sunlight for a long time, accumulating a large amount of low-grade thermal energy, which aggravates environmental pollution and energy consumption. Thermoelectric cement-based composites can realize the interconversion of thermal and electrical energy, showing great potential benefits in large-scale heat collection and energy conversion. Although a lot of exploration and research has been carried out on the thermoelectric properties of cement-based composites reinforced with carbon materials, the contribution of the characteristics of carbon materials, such as the graphitization degree, to the thermoelectric properties of cement-based composites is still unclear. In this article, the graphitization degree of expanded graphite (EG) was modulated by etching EG with an acid solution. The low graphitization degree improves the effective mass of carriers and aggravates the electron and phonon scattering at the interface of EG/cement-based composites. Low thermal conductivity was obtained while increasing the Seebeck coefficient of EG/cement-based composites. The power factor (17.1 μW m-1 K-2) and thermoelectric figure of merit (2.95 × 10-3) of the sample are increased by 18.6 times and 44.2 times, respectively, achieving the highest thermoelectric performance in cement-based composites reinforced with carbon materials. This study provides a direction for improving the thermoelectric properties of cement-based composites by structural regulation of carbon materials.

Fabrication of matrix graphite with a high degree of graphitization for spherical fuel elements by using natural microcrystalline graphite fillers

Matrix graphite is used as a structural material, thermal conductor, moderator, and secondary fission product barrier for fuel elements in high-temperature gas-cooled reactors (HTRs). Due to its high graphitization degree and compressibility, natural flake graphite (NFG) is used as the main filler in traditional A3-3 matrix graphite, whereas artificial graphite (AG), with a lower graphitization degree than NFG, serves as an additive for toughness and gas permeability. Matrix graphite could be improved in terms of thermal conductivity, oxidation resistance, and irradiation performance by increasing the degree of graphitization. However, reports on the development of new matrix graphite formulations are scarce. In this study, MG-20 matrix graphite was prepared by mixing 60 wt% NFG, 20 wt% natural microcrystalline graphite (MG), and 20 wt% phenolic resin. Due to the high graphitization degree (higher than AG) and low coefficient of thermal expansion (CTE) of MG, MG-20 exhibited higher thermal conductivity (∼6%) and lower CTE (∼2.4%) than A3-3. Thus, MG-20 with higher graphitization degree and better thermal properties than A3-3 could improve the performance of HTR fuel elements in the future.

An investigation on purity enhancement through hydrofluoric acid treatment in graphite powder derived from coconut shell

The present research emphasizes a novel approach for synthesizing graphite powder derived from coconut shell (CS) as a precursor, particularly focusing on investigating the effects of hydrofluoric acid (HF) in removing silica and other impurities. The cost-effective pyrolysis technique employed in synthesizing graphite powder entails heating CS to 900 °C, followed by treatment with HF at varying sample-to-acid ratios. Several characterization methods are used to validate the successful synthesis of graphite powder, such as X-ray Diffraction (XRD), Raman Spectroscopy, Fourier-transform Infrared Spectroscopy (FTIR), and Scanning Electron Microscopy (SEM). XRD analysis shows a distinctive graphitic structure, with Gr14 (graphite prepared with a CSCP to HF ratio of 1:4) exhibiting a high graphitization degree of 93.02 %, indicative of excellent crystal structure and high-quality graphite. FTIR analysis of coconut shell charcoal powder (CSCP) reveals the presence of various oxygen-related functional groups, effectively removed by HF washing, leading to graphite with minimal impurities. The Raman spectra of Gr14 demonstrate fewer defects and a more organized structure than other samples. SEM image of CSCP reveals particles with non-uniform morphologies, while the EDX spectra indicate that Gr14 consists of 97.84 % carbon. Treating CSCP with HF enhances the electrical conductivity of the graphite, with Gr14 exhibiting a higher conductivity value. TGA results reveal the improved thermal stability of the graphite. The residual weight of Gr14 is maximum, confirming its exceptional thermal stability and purity. The findings suggest that HF has a significant influence on improving the purity of CS-derived graphite. The study concludes that, among the prepared samples, Gr14 exhibits favorable characteristics, such as minimal impurities, superior crystal structure, higher carbon content, good electrical conductivity, high thermal stability, and fewer defects, comparable to pure graphite. Future research in this study aims to use CS-derived graphite powder for synthesizing nanomaterials like graphene oxide (GO) and reduced graphene oxide (rGO).

Mesoporous N‐Doped Carbon Nanospheres as Anode Material for Sodium Ion Batteries with High Rate Capability and Superior Power Densities

AbstractOptimized sodium ion battery (SIB) carbon anodes with high stability supporting high power densities are a much‐needed material class and therefore intensively researched. The optimum graphitization degree to accommodate sodium ions, while providing high conductivity, as well as the influence of particle size distribution or pore sizes on the performance of carbon anodes, is one of the most discussed topics in this field. While a lot of studies have been published discussing these questions, the convoluted nature of these parameters, originating from material synthesis constraints, usually prevents their independent optimization. Based on Mesoporous N‐doped Carbon Nanospheres (MPNC) as model carbon material systems, the graphitization temperaturefor spherical particles with a monomodal particle size distribution (≈280 nm) and a narrow pore size distribution (≈30 nm) is optimized for faradaic sodium ion storage (plateau capacity) and electrodes with a very high power density of 2680 W kg−1 at 1000 mA g−1 and a remarkable capacity retention over 2000 cycles of 86 %, only losing 0.04 % of its specific capacity per cycle, are demonstrated.

Impact of Organic Sulfur on Coal Graphitization

AbstractThe utilization of high‐sulfur coal, especially high‐organic coal, has always been a difficult hot spot in the energy field. To study the influence of sulfur in coal on coal‐based graphite products, a series of coal samples with different sulfur content and different degrees of coalification were collected for proximate analysis, ultimate analysis, and sulfur species analysis. The structural characteristics of coal‐based graphite products were analyzed by X‐ray diffraction (XRD). The relationships between the sulfur in coal and the yield (Y), graphitization degree (G), cell diameter (La), and stacking height (Lc) of coal‐based graphite products were explored. The yield of coal‐based graphite ranges from 8.92 % to 64.45 %, and it was found that the yield of coal‐based graphite is not only affected by the degree of coalification, fixed carbon content, and volatile matter content of coal but also significantly inhibited by organic sulfur in coal when the reflectance is less than 2.00 %. The graphitization degree (G) of coal‐based graphite is distributed between 76.02 % and 91.02 %, and positively related to the degree of coalification, and negatively related to the content of volatile matter. Organic sulfur in coal is an unfavorable factor for the graphitization degree (G) of coal‐based graphite. Both the cell diameter (La) and stacking height (Lc) of coal‐based graphite are positively correlated with the degree of coalification and negatively correlated with the volatile matter content in coal. Organic sulfur in coal plays an important inhibitory role on the cell diameter (La) of coal‐based graphite. Still, it has almost no effect on the stacking height (Lc) of coal‐based graphite, resulting in a low ratio of horizontal‐to‐vertical (La/Lc), which is not conducive to the horizontal development of coal‐based graphite cells.

Co-pyrolysis of cellulose and lignin: Effects of pyrolysis temperature, residence time, and lignin percentage on the properties of biochar using response surface methodology

Cellulose, hemicellulose, and lignin constitute the basic components of biomass. Knowledge of the interactions between cellulose and lignin during pyrolysis is crucial for unraveling the pyrolysis characteristics of biomass. In this study, for the co-pyrolysis of cellulose and lignin to produce biochar, three influencing factors were selected: pyrolysis temperature (400–800 °C), residence time (5–30 min), and lignin percentage (0–100 %). Pyrolysis experiments were conducted in a vertical tube furnace and the impact of these three factors on the characteristics of biochar was comprehensively explored employing response surface methodology. The results revealed obvious differences between actual values and theoretical values. Specifically, the results showed that the interaction between cellulose and lignin increased the biochar yield, oxygen content, volatile content, and ash content by 6.14 %, 22.85 %, 30.95 %, and 46.75 %, respectively. In contrast, the carbon content, fixed carbon content, and HHV of biochar were relatively reduced by 9.38 %, 11.80 %, and 3.3 %, respectively. Furthermore, Raman spectra of biochar showed that the actual value of graphitization degree of biochar was higher than the theoretical value. This was further corroborated by XPS analysis, wherein owing to the interactions between cellulose and lignin, the actual C-C bond content decreased in contrast to the theoretical value. However, the contents of C-O, CO, COOH functional groups, and aromatic rings increased. Finally, the summary of the co-pyrolysis rules of cellulose and lignin provided a reference for optimal pyrolysis conditions and understanding the mechanism of co-pyrolysis.

Microwave-absorbed porous carbon was prepared from agricultural coconut shell waste by a simple one-step high temperature charring

Coconut shell was a resourceful and renewable biomass waste in our country, which can obtain a rich pore structure after simple charring treatment. In this paper, coconut shell porous carbon (CSPC) material with good wave-absorbing properties was successfully prepared by activating coconut shell powder with KOH and charring at high temperature. The material had a porous structure, honeycomb, with the charring temperature and the proportion of activator gradually increased, the degree of graphitization gradually increased. When the charring temperature was 600 ℃ and the activator ratio was 0.5:1, the minimum reflection loss (RL min) value was −37.23 dB when the sample thickness was 1.5 mm and the test frequency was 16.72 GHz. The coconut shell porous carbon prepared was a new type of electromagnetic wave-absorbing material made from agricultural waste, which can obtain a better microwave absorption effect after simple processing.

Machine learning-assisted thermomechanical coupling fabrication of hard carbon for sodium-ion batteries

This study conducts an extensive investigation into the application of hard carbon in sodium-ion batteries. More than 100 hard carbon samples are meticulously synthesized by precisely controlling temperature and pressure, and their microstructure and performance are comprehensively evaluated. This research introduced innovative standardized parameters, including degree of graphitization, degree of crystallinity and degree of defect, which can be universally applied to the field of amorphous carbon materials. Furthermore, the utilization of machine learning facilitates rapid prediction and screening of high-performance hard carbon materials. As a result, a fully optimized hard carbon anode is successfully developed. At a current density of 0.03 A g−1, the material demonstrates a reversible capacity of 375 mAh g−1 and an initial coulombic efficiency of 92.3 %. At a high current rate of 2 A g−1, it delivers a capacity of 250 mAh g−1. The investigation further provides robust evidence for the pore-filling mechanism of Na clusters by in situ spectroscopic studies. This study not only introduces novel approaches for controlling and quantifying the microstructure of hard carbon but also demonstrates a case study of efficient material development by machine learning.

Imidacloprid removal by modified graphitic biochar with Fe/Zn bimetallic oxides

Coping with the critical challenge of imidacloprid (IMI) contamination in sewage treatment and farmland drainage purification, this study presents a pioneering development of an advanced modified graphitic white melon seed shells biochar (Fe/Zn@WBC). The Fe/Zn@WBC demonstrates a substantial enhancement in adsorption efficiency for IMI, achieving a remarkable removal rate of 87.69% within 30 min and a significantly higher initial adsorption rate parameter h = 4.176 mg g−1·min−1. This significant improvement outperforms WBC (12.22%, h = 0.115 mg g−1·min−1) and highlights the influence of optimized adsorption conditions at 900 °C and the graphitization degree resulting from Fe/Zn bimetallic oxide modification. Characterization analysis and batch sorption experiments including kinetics, isotherms, thermodynamics and pH factors illustrate that chemical adsorption is the main type of adsorption mechanism responsible for this superior ability to remove IMI through pore filling, hydrogen bonding, hydrophobic interaction, electrostatics interaction, π-π interactions as well as complexation processes. Furthermore, we demonstrate exceptional stability of Fe/Zn@WBC across a broad pH range (pH = 3–11), co-existing ions presence along with humic acid under various real water conditions while maintaining high removal efficiency. This study presents an advanced biochar adsorbent, Fe/Zn@WBC, with efficient adsorption capacity and easy preparation. Through three regeneration cycles via pyrolysis method, it demonstrates excellent pyrolysis regeneration capabilities with an average removal efficiency of 92.02%. The magnetic properties enable rapid separation facilitated by magnetic analysis. By elucidating the efficacy and mechanistic foundations of Fe/Zn@WBC, this research significantly contributes to the field of environmental remediation by providing a scalable solution for IMI removal and enhancing scientific understanding of bimetallic oxides-hydrophilic organic pollutant interactions.

Straw-derived macroporous biochar as high-performance anode in microbial fuel cells

Large-scale application of MFCs is limited by the high cost of electrode and low power density. In this study, the electrochemical structure and power output performance of three novel straw-derived biochar are discussed and characterized by scanning electron microscope, specific surface area, cyclic voltammetry, Raman spectrum, electrochemical impedance spectroscopy etc. Compared with the common carbon felt electrode, the optimal electricity generation ability and electrochemical affinity are obtained in corn straw biochar electrode: the rough surface with macroporous structure and high degree of graphitization facilitates the attachment of electroactive bacteria; the maximum output voltage, open circuit voltage, power density and coulombic efficiency reach 662.64±4.03 mV, 798.24±3.65 mV, 1.54±0.18 W m−2 and 50.39±1.68 %, respectively; the maximum COD removal efficiency of 77.45±1.69 % is achieved; exchange current density (4.6142×10−4 A cm−2) in corn straw electrode presents the better electrochemical activity than that of carbon felt electrode. These implies that corn straw-derived biochar is a competitive raw material for MFC anode.

Enhanced energy efficiency and fast co-pyrolysis characteristics of biogas residues and long-flame coal using infrared heating and TG-FTIR-MS

Co-pyrolysis may enhance the energy efficiency of anaerobic digestion waste (biogas residues), while simultaneously facilitating the clean utilization of coal. A thermogravimetric analyzer (TG), TG-FTIR-MS, and infrared heating technique were employed to investigate the rapid co-pyrolysis properties of long-flame coal (LFC) and biogas residues (BR) in this study. Meanwhile, the effects of temperature on the co-pyrolysis product distributions and compositions were studied in reactors that were heated with electric heating and rapid infrared heating. The co-pyrolysis of LFC and BR had the potential to decrease greenhouse gas emissions, as indicated by the TG-FTIR/MS findings. The co-pyrolysis kinetics were calculated using two models (KAS and FWO); the average Eα values are 176.09 and 187.26 kJ/mol, respectively. Tar yields increased initially in IH (electric heating) and EH (infrared heating) reactors, before declining as the temperature rose. The tar yields are greatest for EH at 500 °C (16.12 wt%) and IH at 600 °C (16.02 wt%). Tar yields generated via infrared heating were greatly higher than those generated by EH at 600–700 ℃. IH has a higher tar yield due to the fact that there are significant synergistic effects between coal and lignin, protein, and lipid at high temperatures. The GC-MS results indicate that IH has promoted the aromatization and ketonization reactions. Moreover, more monocyclic aromatic and bicyclic aromatic products are generated by infrared heating, suggesting an indication of tar quality improvement. An elevated co-pyrolysis temperature results in a greater degree of graphitization in char.

Low resistance bisphenol-A based polybenzoxazine derived laser-induced graphene (LIG) and its microsupercapacitor application

Herein, we demonstrate the use of conventional BA-a based polybenzoxazine as a laser-induced graphene (LIG) forming precursor. The effects of laser power and the engraving speed on formation and properties of LIG are explored. By optimizing the laser fluency related to laser power along with engraving speed, poly(BA-a) derived LIG with high graphitization degree and low sheet resistance (Rs) of ∼ 2–10 Ω/sq can be acquired. The morphologies and surface area of LIGs in such low Rs region are then validated through SEM and BET, respectively. The resulting poly(BA-a) derived LIG exhibits a high amount of macropores in the structure with marginal differences in the specific surface area being 27–88 m2/g. In addition, electrochemical performances of the two-electrode based microsupercapacitor (LIG-MSC) of the selected samples in low Rs region with different specific surface area are evaluated. The LIG-MSC shows a specific capacitance of 1.39 mF/cm2 (0.04 mA/cm2), and good cycling stability of 10,000 cycles with capacitance retention of 92% (0.2 mA/cm2). Our results highlight that poly(BA-a) derived LIG is promising for high performance LIG applications.

Unlocking the influence of pitch-based and acetylene-based carbon coating on the electrochemical performance of SiO anodes: bridging insights from half-cell to full-cell studies

Silicon monoxide (SiO) has garnered significant attention as a prominent candidate for high-energy-density lithium-ion batteries (LIBs) owing to its reduced volume expansion and enhanced cycling stability compared to pure silicon (Si). However, the effect of carbon layers derived from different carbon sources on the electrochemical performance of SiO in both half and full cells has not been comprehensively studied, and the industrial consensus regarding the selection of carbon sources for SiO remains elusive. Herein, a systematic comparative evaluation was conducted to analyze the physicochemical properties and electrochemical behaviors of SiO with two different carbon layers. Additionally, comprehensive assessments were carried out to investigate the electrochemical performance of SiO employing two distinct carbon coating methods in 6 Ah pouch full-cell configurations, where SiO coated acetylene-based carbon exhibits advantages in cycling stability and Li+ kinetic. In industrial SiO carbon coating processes, it is advisable to prioritize acetylene-derived carbon using chemical vapor deposition (CVD) characterized by a high degree of graphitization, enhanced electrical conductivity, and uniform surface coverage. The investigation rooted in electrochemical performance of different carbon layers on SiO in both half-cell and full-cell configurations, provides fundamental insights for the advancement of research in silicon-based anodes’ development.

Thermal-mechanical evolution behaviors of metal matrix diamond composite by powder bed fusion-laser beam

The thermal damage of diamond and the residual stress have always been the critical issues to be resolved in the development of metal matrix diamond composites. In the presented study, FeCoCrNi high entropy alloys (HEAs)-diamond composites were fabricated by powder bed fusion-laser beam of metals (PBF-LB/M), using un-coated diamond and Ti–Ni coated diamond, respectively. Based on the numerical and experimental analysis, the effect of thermal-mechanical behavior on the microstructures and mechanical properties of the composites was systematically investigated. By establishing the temperature field of the PBF-LB molten pool, the defects, diamond graphitization and in-situ TiC formation were studied. The start-temperature for diamond graphitization in coated samples was 365 °C higher than that of un-coated samples, due to the diffusion barrier effect of TiC. Subsequently, by thermo-mechanical coupling, the property and value of the residual stress exhibited sudden change at the diamond/matrix interface. The TiC intermediate layer significantly relieved the stress concentration at interface, and effectively avoided cleavage fracture of the diamond and the initiation of interfacial cracks. At the moderate molten-pool temperature, the coated diamond composites exhibited optimal performance, as bending strength of 913 MPa, friction coefficient of 0.25 and worn mass loss of 0.67 mg. Finally, the quantitative relationship between PBF-LB molten-pool temperature and the relative density, graphitization degree, residual stress, retention(bending strength) and wear performance was established, to demonstrate the thermal-mechanical evolution of the HEAs-diamond composites by PBF-LB.

Spatial confinement and erbium-mediated electronic modulation for enhanced 4-nitrophenol destruction through peroxymonosulfate activation

The development of efficient strategies to modulate the electron structure of active sites in heterogeneous catalysts is crucial but remains challenging for enhancing peroxomonosulfate (PMS) activation to degrade organic contaminants. In this study, Co-Er-N-doped carbon black materials are successfully synthesized by pyrolyzing the CB@Er/Co-complex precursor. Er-doping does not enhance the defect level or graphitization degree of the carbon matrix, but rather regulates the electronic structure of Co sites, thereby generating abundant metallic Co species for activating PMS and yield increased reactive oxygen species towards 4-nitrophenol (4-NP) degradation. The optimal Er/Co@NCB-0.6 catalyst exhibits a removal efficiency of 97.9 % in 20 min. Furthermore, this catalyst exhibits broad degradation capabilities against various organic contaminants. Due to the spatial confinement effect from carbon layers, the encapsulated Co nanoparticles in the Er/Co@NCB-0.6 catalyst demonstrate excellent stability and reusability for the reaction. Radical quenching and electron paramagnetic resonance results indicate that the Er/Co@NCB-0.6/PMS system involves radical and non-radical pathways, and 1O2 and SO4•− play essential role in degrading 4-NP. The pollutant is degraded into seventeen intermediates via two plausible pathways. This study provides a valuable rare metal-mediated strategy to regulate the electronic structure of Co-based catalytic materials towards activating PMS in removing persistent organic pollutants.

Absorption frequency band switchable intelligent electromagnetic wave absorbing carbon composite by cobalt confined catalysis

The dielectric loss of carbon materials is closely related to the microstructure and the degree of crystallization, and the microstructure modulation of electromagnetic wave absorbing carbon materials is the key to enhancing absorption properties. In this work, a porous elastic Co@CNF-PDMS composite was prepared by freeze-drying and confined catalysis. The graphitization degree and conductivity loss of carbon nanofibers (CNFs) were regulated by heat treatment temperature and Co catalyst content. The construction of a heterointerface between Co and C enhances the interfacial polarization loss. The Co@CNF-PDMS composite with 4.5 mm achieves the minimum reflection loss (RLmin) of –81.0 dB at 9.9 GHz and RL no higher than –12.1 dB in the whole of the X-band. After applying a load of up to 40 % strain and 100 cycles to Co@CNF-PDMS, the dielectric properties of the composite remain stable. With the increase of compression strain, the distribution density of the absorbent increases, and the CNF sheet layer extrusion contact forms a conductive path, which leads to the conductive loss increase, finally, the absorption band moves to a high frequency. The absorption band can be bi-directionally regulated by loading and strain with good stability, which provides a new strategy for the development of intelligent electromagnetic wave absorbing materials.

Effects of adding n-amyl alcohol, dimethylfuran to fuel on soot formation in aviation kerosene diffusion flame

As the main energy consumption of aviation and aerospace, the study of combustion characteristics of aviation kerosene is of great significance. In this paper, through the self-built experimental system, the combustion flame characteristics of pure aviation kerosene, aviation kerosene mixed with n-amyl alcohol, aviation kerosene mixed with dimethylfuran were studied under different working conditions, and the physicochemical properties of soot particles generated in the flame, and the effects of mixing n-amyl alcohol and dimethylfuran on the formation of soot particles were analyzed from the microscopic perspective. The results show that: 1. The soot particles in the combustion of aviation kerosene mixed with n-amyl alcohol and dimethylfuran show some characteristics of amorphous structure, unclear outline and incomplete curing; 2. Under K-D20 condition, nitrates are included in particulate matter generated by soot; 3. After mixing n-amyl alcohol and dimethylfuran, the degree of graphitization continues to decrease.