Pyrolytic Graphite Research Articles

Application of DPG/KH550 modified pyrolysis carbon black in oil and high temperature‐resistant NBR composites

AbstractIn this paper, pyrolysis carbon black (CBp) was introduced into nitrile butadiene rubber (NBR), the effects of the ratio of CBp and carbon black (N326) on the properties of NBR composites were investigated, and the optimal ratio was determined. On this basis, the accelerator DPG, coupling agent KH550 and CBp were modified by ball milling and plasma. The results showed that when the ratio of CBp to N326 was 40:15, the overall properties of NBR composites was better. Compared with the unmodified CBp/NBR composites, the change rate of tensile product, resilience and DIN abrasion of ball milling‐plasma modified CBp/NBR composites in oil environment were reduced by 52.96%, 12.81%, and 27.19%, respectively, and the tear strength after double damage by high temperature and oil bath was increased by 15.63%, which resulted in better oil and high temperature‐resistance. In summary, the ball milling‐plasma combined with DPG/KH550 modified CBp can not only replace N326 carbon black, but also realize the preparation of NBR composites with better oil and high temperature‐resistance.

Low-temperature treatment optimization for diesel-contaminated kaolin: Mutual impacts of generated pyrolytic carbon and particle agglomeration

Efficiency improvement in low-temperature treatment for diesel-contaminated sites is urgent because changes in soil properties and the generation of new substance during the remediation process can influence the duration and energy utilization. This paper focuses on low-temperature treatment optimization based on the mutual impacts of pyrolytic carbon and kaolin aggregation. Results reveal that the peak mass loss rate occurred between 100–150°C, with minimal loss beyond 200°C. Samples thermally treated at 150–200°C exhibited darker colors, indicating pyrolytic carbon formation, corroborated by x-ray photoelectron spectroscopy (XPS), fourier transform infrared spectroscopy (FTIR), and three-dimensional fluorescence spectrum (3D-EEM) analyses. Additionally, diesel contamination influenced the fractal dimension of aggregates by influencing adhesion forces (<10000 mg/kg) and forming liquid bridges (≥10000 mg/kg) in untreated kaolin, resulting in an initial increase and subsequent fall in fractal dimension with increasing concentration. Decline rates of pollutant gas concentration were closely correlated with fractal dimension changes under thermal conditions due to pollutant volatilization and pyrolytic carbon formation. Based on the consistency between fractal dimension and decline rate, two critical remediation concentrations (C0) and temperatures (T0) indices were identified to optimize the low-temperature remediation.

Mechanical properties and microstructure of quartz fiber-reinforced silica matrix composite with a single layer pyrocarbon interphase

Silica matrix composites (SiO2f/SiO2), reinforced with pyrolytic carbon (PyC) interfacial layers, were synthesized using the precursor impregnation and pyrolysis (PIP) method, mechanical properties and microstructure of these composites were thoroughly investigated. The flexural strength of SiO2f/PyC/SiO2 composites exceeded 55 MPa after treatment at 450°C. Notably, at medium and high temperatures, strength of SiO2f/SiO2 composites was significantly enhanced compared to that of uncoated PyC composites. The experimental resulted indicate that PyC temporary interfacial layer effectively mitigated the strong interfacial reaction between quartz fibers and matrix. Furthermore, fiber pull-out phenomenon observed at the fracture of SiO2f/PyC/SiO2 composites suggested that interfacial bonding was weak, which contributed to the high mechanical strength of these composites.

Spatial confinement strategy modulated by kinetic diameters of gaseous molecules for sodium storage

Constructing closed pore structures is essential for improving the plateau capacity of high-capacity hard carbon (HC) anodes for sodium-ion batteries. However, the absence of a straightforward and efficient strategy for constructing closed pores has hindered the advancement of high-capacity HC anodes. Here, we have developed a spatial confinement strategy for constructing closed pore structures using pyrolytic carbon (PC) as substrate and pyrolysis gas as the carbon source for chemical vapor deposition. The deposition of pyrolysis gas effectively tightens the pore entrance, thereby preventing electrolyte infiltration and transforming the open pores in the PC into highly efficient sites for sodium storage. The obtained optimal anodes demonstrate a remarkable specific capacity of 324.6 mAh g-1. More importantly, we calculate the kinetic diameters of the carbon source molecules from their iso-electron density surfaces and correlate them with the mechanism of closed pore formation, which will effectively guide the fabrication of closed pores for sodium storage.

Biochar: Preserving the Long-Term Catalytic Activity of Biosynthesized PdNPs/AuNPs in Cr(VI) Reduction

Palladium nanoparticles (PdNPs) and gold nanoparticles (AuNPs) synthesized within yeast biomass can be effectively preserved in yeast biochar while maintaining their catalytic activity. Herein, we observe well-preserved PdNPs/AuNPs within yeast biochars, alongside the retention of cell morphology. Notably, the crystal structures of AuNPs within biochars exhibit similarity to that of uncarbonized samples, suggesting minimal influence of carbonization on nanoparticle structure. XPS analysis reveals the transformation of organic bacterial cells into heterocyclic aromatic-carbon material during pyrolytic carbonization. Chemical states analysis indicates the prevalence of metallic Pd(0)/Au(0) with limited PdOx/AuOx content in yeast biochars. FTIR analysis highlights increased aromaticity of biochars with typical bands for aromatic ring, and new bands appeared in Pd/Au-loaded biochars possibly attribute to PdOx/AuOx. Moreover, yeast biochars exhibit significantly improved Cr(VI) removal capacities compared to yeast biomass. Specifically, we detect complete removal within 18h for CYPd and CYPdG biochars, contrasting with less than 65% removal efficiency in yeast biomass. These findings underscore the potential of carbonization in enhancing the long-term catalytic activity of biosynthesized PdNPs/AuNPs for efficient Cr(VI) reduction, offering promising avenues for environmental remediation strategies.

Biochar from Malt Residue: Toward a Circular Economy for Sustainable Fluoroquinolone Removal in Aqueous Systems

Malt bagasse holds potential as a high-value material, contributing to a circular economy. Biochars were synthesized via pyrolysis (PC-500) and hydrothermal carbonization (HC-150), with one-pot activation using phosphoric acid. Additionally, PC-500 activated with H3PO4 was synthesized for comparison. Various analytical methods were used to characterize the materials. The PC-500 and PCA-500 samples exhibited higher degrees of carbonization, whereas the HC-150 sample retained its functional groups more effectively. Biochars showed higher porosity than biomass, with microspheres present in HC-150. Evaluations were conducted on the removal of fluoroquinolones from water using biochars. Maximum removal efficiency was obtained at pH 8, favoring neutral fluoroquinolone species with a Brønsted acid-base nature. The experimental outcomes were further rationalized by the computational calculation of the physicochemical properties of the adsorbates, in analogy with the structural activity relationship approach in medicinal chemistry. The pseudo-second-order kinetic model proved to be the most suitable for fitting the experimental data, while the Langmuir model effectively described the adsorption isotherms. Ciprofloxacin, enrofloxacin, and norfloxacin showed maximum adsorption capacities (qmax) of 95, 164, and 99mgg-1, respectively, when HC-150 was used. On the other hand, with PC-500, qmax of 57, 12, and 20mgg-1 were obtained for ciprofloxacin, enrofloxacin, and norfloxacin, respectively. Although PCA-500 enhanced adsorption capacity compared to PC-500, the qmax remained lower than the results obtained with HC-500, measuring at 51, 102, and 95mgg-1. These findings emphasize malt bagasse biochar as a viable adsorbent.

Effects of different low-temperature pyrolysis treatments on the biotoxicity of biochar derived from tobacco stalks

The pyrolytic treatment of tobacco stalk (TS) waste results in the production of a large amount of biochar, which is usually used for environmental remediation. However, little attention has been given to the effects of different pyrolysis methods on the biotoxicity of TS biochar. This study examined the effects of three different pyrolysis methods at 350 °C (fast pyrolysis, slow pyrolysis, and low-temperature carbonization) on the biotoxicity of TS biochar (Escherichia coli (E. coli) growth and wheat germination). The results revealed that the dissolved organic matter (DOM) of the three types of biochar promoted the growth of E. coli, and the maximum growth of E. coli was ranked as DOM-F350 > DOM-S350 > DOM-350. However, the DOM inhibited the growth of the wheat seeds, with the growth index (below 0.8) of the wheat seeds ranked as DOM-350 > DOM-F350 > DOM-S350. The alkali metal content, pH and humus-like substance content of biochar may be responsible for the biotoxicity of biochar through various mechanisms. In addition, TS-S350 exhibited greater biotoxicity than did TS-F350 because of the greater content of toxic nitrogen-containing organic compounds. These findings can provide reliable theoretical guidance for the effective management and safe utilization of TS waste.

Nano-thick surface-modified layer governs bending deformation of micrographite

This study aimed to investigate the impact of surface-modified layer (SML) on the bending deformation of van der Waals (vdW)-stacked materials. Bending tests were conducted on micrographite (highly oriented pyrolytic graphite, HOPG) cantilevers with controlled SML thickness using various ion beam irradiation conditions. Irradiation of the HOPG surface with ion beams at accelerating voltages of 30, 5 and 0.1 kV resulted in the formation of SMLs with thicknesses of approximately 10, 5 and less than 3 nm, respectively. Microcantilever-beam specimens with SML thicknesses of less than 3 nm and approximately 5 nm exhibited shear deformation with localized interlayer slip. In contrast, specimens with a thickness of approximately 10 nm showed no interlayer slip, with bending deformation dominating. This transition was attributed to the increase in SML thickness. The nominal shear modulus increased by a factor of approximately 1.58 and 2.23 for specimens with SML thicknesses of approximately 5 and 10 nm, respectively, compared with those with thicknesses of less than 3 nm. The resistance to subsequent nonlinear deformation also increased with thicker SML. These results indicate that the presence of SMLs of only a few nanometers to 10 nm suppressed interlayer slip and significantly enhanced the deformation resistance of micro-HOPGs.

Characterizing the surface compositions of supported bimetallic PtSn clusters: Effects of cluster-support interactions and surface adsorbates

PtSn bimetallic clusters on TiO2(110) and highly oriented pyrolytic graphite (HOPG) surfaces have been characterized by scanning tunneling microscopy, low energy ion scattering (LEIS), X-ray photoelectron spectroscopy, and temperature programmed desorption (TPD); density functional theory (DFT) calculations have also been performed to better understand adsorption of CO and D2 on the PtSn surfaces. On TiO2 at coverages of 2 ML of Pt and 2 ML of Sn, exclusively bimetallic clusters are formed for both orders of deposition because clusters of the first metal completely cover the surface such that all atoms of the second metal are incorporated into the existing clusters. In contrast, on HOPG, the high mobility and weak cluster-support interactions on HOPG result in much larger 2 ML monometallic clusters (∼30 Å high) that do not completely cover the surface, and deposition of the second metal produces larger clusters as well as smaller ones. Despite the difference in cluster morphologies for the different orders of deposition and supports, the LEIS experiments demonstrate that in all cases, the PtSn clusters are rich in Sn at the surface, as expected based on the lower surface free energy for Sn compared to Pt. Furthermore, the +0.2 eV shift in the Sn(3d5/2) binding energy observed on all surfaces in the presence of Pt is consistent with PtSn alloy formation. Deposition of 2 ML of Sn on TiO2 produces two-dimensional clusters with oxidation of Sn and reduction of titania at the cluster-support interface, but addition of Pt to the Sn clusters causes Sn to diffuse away from this interface, leaving Sn in the metallic state. TPD experiments on 2 ML Pt/TiO2 with increasing coverages of Sn show that the number of adsorption sites for D2 sharply decreases to nearly zero at 0.5 ML, while CO adsorption decreases to zero only at much higher Sn coverages of 2 ML. DFT studies for Sn modified Pt surfaces and bulk structures demonstrate that for CO adsorption at low Sn coverages (≤0.25 ML), the strong Pt-CO interactions induce diffusion of Pt to the cluster surface and the formation of a bulk Pt3Sn alloy, whereas D2 adsorption does not lead to interactions with the Pt surface that are strong enough to induce alloy formation. A single Sn adatom prevents D2 adsorption on four neighboring Pt atoms via site-blocking and the donation of electron density to Pt.

Self-doped Na-carbon materials derived from a lyocell fiber for a high-performance trimethylamine gas sensor at room temperature

In this study, biomass-derived carbon material obtained from Lyocell fibers was first utilized as a gas sensor. The impacts of varying pyrolytic carbonization temperatures and pregrinding treatments on the structure, surface morphology, elemental composition, and gas sensitivity of the samples were thoroughly examined. The CL-500 sensor can realize rapid detection of trimethylamine with a high response (12.79k%, 500 ppm) and high selectivity at room temperature; the response/recovery times are 10 s and 2 s, respectively, and the theoretical detection limit is 3.96 ppm. Moreover, after four months, the response of the CL-500 sensor to trimethylamine fluctuated by less than 9.7 % compared with that of the fresh sensor, indicating good stability. It also shows good recovery after seven consecutive response-recovery cycles. Additionally, the CL-500 sensor has promising applications in real-life fish freshness monitoring. Theoretical calculations indicate that the introduction of trace amounts of Na enhances the sensing performance of this sensor for target gases. This study serves as a guide for developing cost-effective, high-performance gas sensors, promoting the efficient and high-value utilization of biomass waste.

Influence of Carbon Content on Element Diffusion in Silicon Carbide-Based TRISO Composite Fuel

The coating layers of Tri-structural Isotropic Particles (TRISO) serve to protect the kernel and act as barriers to fission products. Sintering aids in the silicon carbide matrix variably react with TRISO coating layers, leading to the destruction of the coating layers. Investigating how carbon content affects element diffusion in silicon carbide-based TRISO composite fuel is of great significance for predicting reactor safety. In this study, silicon carbide-based TRISO composite fuels with different carbon contents were prepared by adding varying amounts of phenolic resin to the silicon carbide matrix. X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM) were employed to characterize the phase composition, morphology, and microstructure of the composite fuels. The elemental content in each coating layer of TRISO was quantified using Energy-Dispersive X-ray Spectroscopy (EDS). The results demonstrated that the addition of phenolic resin promoted the uniform distribution of sintering aids in the silicon carbide matrix. The atomic percentage (at.%) of aluminum (Al) in the pyrolytic carbon layer of the TRISO particles reached its lowest value of 0.55% when the phenolic resin addition was 1%. This is because the addition of phenolic resin caused the Al and silicon (Si) in the matrix to preferentially react with the carbon in the phenolic resin to form a metastable liquid phase, rather than preferentially consuming the pyrolytic carbon in the outer coating layer of the TRISO particles. The findings suggest that carbon addition through phenolic resin incorporation can effectively mitigate the deleterious reactions between the TRISO coating layers and sintering aids, thereby enhancing the durability and safety of silicon carbide-based TRISO composite fuels.

Improved demineralization of the carbon black obtained from the pyrolysis of the sidewall and tread of scrap Tires: Extraction of some micro-/macro-nutrient elements of plants

In parallel with the increasing tyre production in the world, the amount of scrap tyres is also increasing. Within the scope of scrap tyre management, studies aimed at preventing the accumulation of tyres that threaten the world in terms of human health and the environment can be briefly defined as 4RL, including recycling, reuse, recovery, regeneration, landfill. Current methods have not yet completely controlled the accumulation of scrap tires. In this study, sidewall and tread parts of scrap tires with different compositions were pyrolyzed separately. Pyrolytic carbon black has been upgraded with an improved acid-base extraction method. Two different carbon blacks of high commercial value were obtained from the tire sidewall and tread. Since the mixture obtained from acidic-basic extraction, consisting of elements such as Zn, K, Na, Ca and S, are micro and macro nutrients of plants, the solution can be used directly in the fertilizer industry. With this study, the commercial value of solid residue, which is a major bottleneck in tire pyrolysis plants, has been increased. The pyrolysis method has been transformed into a more feasible project.

Peroxymonosulfate Activation by Fe@N Co-Doped Biochar for the Degradation of Sulfamethoxazole: The Key Role of Pyrrolic N

In this study, Fe, N co-doped biochar (Fe@N co-doped BC) was synthesized by the carbonization–pyrolysis method and used as a carbocatalyst to activate peroxymonosulfate (PMS) for sulfamethoxazole (SMX) removal. In the Fe@N co-doped BC/PMS system, the degradation efficiency of SMX (10.0 mg·L−1) was 90.2% within 40 min under optimal conditions. Radical quenching experiments and electron spin resonance (ESR) analysis suggested that sulfate radicals (SO4•−), hydroxyl radicals (•OH), and singlet oxygen (1O2) participated in the degradation process. After the reaction, the proportion of pyrrolic N decreased from 57.9% to 27.1%. Pyrrolic N served as an active site to break the inert carbon network structure and promote the generation of reactive oxygen species (ROS). In addition, pyrrolic N showed a stronger interaction with PMS and significantly reduced the activation energy required for the reaction (∆G = 23.54 kcal/mol). The utilization potentiality of Fe@N co-doped BC was systematically evaluated in terms of its reusability and selectivity to organics. Finally, the intermediates of SMX were also detected.

Decoding organic compounds in lava tube sulfates to understand potential biomarkers in the Martian subsurface

Exploring molecular biomarkers in lava tube speleothems offers insights into environmental dynamics, biogeochemical processes, and subsurface life, with implications for astrobiology, particularly in Martian analog environments. Despite extensive biomarker research in marine and terrestrial settings, lava tube studies are limited. This study employed molecular, isotope and mineralogical characterization to analyze sulfate speleothems from six lava tubes of Lanzarote (Canary Islands), considered analog for the Moon and Mars. The combination of mass spectrometry, thermogravimetry, and mineralogical techniques, revealed geological processes, biomarkers and their biological sources. The identified minerals were primarily calcium and sodium sulfates. Sulfur isotope analyses indicated volcanic and oceanic origins, while carbon isotope composition and pyrolysis analyses suggested influences from vegetation and microbial activity. Lipidic profiles highlighted branched and n-alkanes, as well as palmitic and stearic acid methyl esters, suggesting microbial origins. These findings contribute to understanding geological and environmental dynamics in lava tubes and recognizing potential biosignatures on Earth and other planets.

Controllable photoexfoliation of monolayer graphene quantum dots using temporally and spatially shaped femtosecond laser

Graphene quantum dots (GQDs) have displayed significant momentum in numerous fields due to their unique electronic properties. However, how to obtain uniformly monolayer quantum dots and explain the synthesis mechanism are still a key technical problem. Here, a rapid and controllable photoexfoliation rate of monolayer graphene quantum dots of up to 80 % was achieved by using temporally and spatially shaped femtosecond laser to ablate bulk highly oriented pyrolytic graphite targets in liquid. Theoretical calculations suggested that the temporally shaped laser can minimize the spatial range of electron excitation, maximize the Coulomb repulsion between the outer layers and Coulomb explosion within the topmost layer through multi-level electron excitation. The above multilevel photoexfoliations lead to the formation of monolayer GQDs. These findings demonstrate a perfect theoretical explanation of controllable and rapid preparation of monolayer quantum dots, accelerating its industrialization in energy storage devices.

Room-temperature superconductivity in carbons – a mini review

The search for room-temperature superconductivity in carbons is gathering momentum because it has a long history, impressive track record, clear advancement route, and theoretical backup. The report of a suspected Josephson current in Al-C-Al sandwiches at room temperature, published in Nature 50 years ago, led to the report of a voltage in nano-graphite films believed to mark the reverse Josephson effect. The report on oxygen-doped diamonds led to full-blown superconductivity in boron-doped diamonds. The reports on highly oriented pyrolytic graphite (HOPG) and water-treated graphite powder led to the claim of a current running by itself for 50 days in a ring of HOPG soaked with alkane at room temperature. It also led to a claim of a current running for 1,000 seconds in a ring of graphene soaked in hexane. The carbons are amicable to intercalation chemistry, electrostatic carrier doping, and surface-proving techniques to promote an increase in carrier density, metallization, and applicability of the Ashcroft proposal. Consequently, the high Debye temperatures (1,670, 2,230 and 2,500 K in graphene, diamond and HOPG) may be sufficient to underwrite superconductivity at T∼300 K in carbons, provided the phonon-exchange factor, λ, is around 3 to mark strong enough interactions between electrons and phonons.

Green Power: The Role of Plant-Based Biochar in Advanced Energy Storage.

This comprehensive review aims to provide an overview of recent progress in utilizing plant-based biochar for supercapacitors. It specifically focuses on biochar derived from plant biomass such as agricultural residues, weeds and aquatic plants, examining their potential in energy storage applications. It explores various synthesis methods like pyrolysis and hydrothermal carbonization and evaluates their impact on biochar's structure and electrochemical properties. Additionally, it examines the electrochemical performance of biochar-based supercapacitors, focusing on parameters such as capacitance, cycling stability, and rate capability. Strategies to enhance biochar's electrochemical performance, such as surface modification and composite fabrication, are also discussed. Furthermore, it addresses existing challenges and prospects in harnessing plant-based biochar for supercapacitor applications, highlighting its potential as a sustainable and efficient electrode material for next-generation energy storage devices.

Synthesis of ZrB2-SiC-ZrC composite powders with core-shell structure via sol-gel molecular modulation

In this study, ZrB2-SiC-ZrC (ZSZ) composite powders with molar ratios C/(B + Zr + Si) = 1.5, 1.9 and 2.4 were obtained by sol-gel method and boro/carbothermal reduction reaction. Meanwhile, the impact of heat treatment temperature (1100 °C–1600 °C) and holding time (1 h–2.5 h) on the resulting powders were studied. The results showed that the ZSZ powder precursors were first completely converted to ZrO2, SiO2, B2O3 and pyrolytic carbon after heat treatment at 1200 °C under the optimized molar ratio (2.4) and holding time (2.5 h). Then, the transformed oxidation products and pyrolytic carbon were completely transformed into ZSZ composite powders after optimized heat treatment at 1500 °C. The synthesized ZSZ composite powders are characterized by the core-shell structure, in which ZSZ particles act as the inner core are encapsulated by the low-crystalline ZrB2 phase as the outer shell to form a core shell structure. The ZSZ composite ceramic materials prepared using the core-shell structural powders have excellent ablative properties in the range of 2000 °C, with the mass and line ablation rate of −3.5 × 10−4 g/cm3 and 2.39 × 10−3 mm/s, respectively.

Microcrystalline Engineering of Anthracite-Based Carbon Via Salt-Assisted Ball Milling for Enhanced Sodium Storage Performance.

Coal-based carbon material, characterized by abundant resources and low cost, has gained considerable interests as a promising anode candidate for sodium-ion batteries (SIBs). However, the coal-based carbon generally shows inferior Na-storage performance due to its highly-ordered microstructure with narrow interlayer spacing. Herein, a salt-assisted mechanical ball-milling strategy is proposed to disrupt the polycyclic aromatic hydrocarbon structure in anthracite molecules, thereby reducing the microcrystalline regularity of the derived carbon during following pyrolysis process. In addition, the induced C─O─C bonds during ball-milling process can alter the pyrolysis behavior of anthracite and restrain the formation of surface defects. Consequently, in contrast to pristine anthracite-based pyrolytic carbon, which exhibits a Na-storage capacity of 198.4 mAh g-1 with a low initial Coulombic efficiency (ICE) of 65.1%, the ball-milling modified carbon assisted by NaCl salt (NAC), with enhanced structural disordering and reduced surface defects, demonstrate significantly improved Na-storage capacity of 332.1 mAh g-1 and ICE value of 82.0%. The NAC electrode also realizes excellent cycle and rate performance, retaining a capacity of 196.0 mAh g-1 at 1 C after 1000 cycles. Furthermore, when coupled with NaNi1/3Fe1/3Mn1/3O2 cathode, the assembled Na-ion full cell deliveres an exceptional electrochemical performance, highlighting its promising prospect as high-performance anode for SIBs.

Numerical Assessment of Effective Elastic Properties of Needled Carbon/Carbon Composites Based on a Multiscale Method

Needled carbon/carbon composites contain complex microstructures such as irregular pores, anisotropic pyrolytic carbon, and interphases between fibers and pyrolytic carbon matrices. Additionally, these composites have hierarchical structures including weftless plies, short-cut fiber plies, and needled regions. To predict the effective elastic properties of needled carbon/carbon composites, this paper proposes a novel sequential multiscale method. At the microscale, representative volume element (RVE) models are established based on the microstructures of the weftless ply, short-cut fiber ply, and needled region, respectively. In the microscale RVE model, a modified Voronoi tessellation method is developed to characterize anisotropic pyrolytic carbon matrices. At the macroscale, an RVE model containing hierarchical structures is developed to predict the effective elastic properties of needled carbon/carbon composites. For the data interaction between scales, the homogenization results of microscale models are used as inputs for the macroscale model. By comparing these against the experimental results, the proposed multiscale model is validated. Furthermore, the effect of porosity on the effective elastic properties of needled carbon/carbon composites is investigated based on the multiscale model. The results show that the effective elastic properties of needled carbon/carbon composites decrease with the increase in porosity, but the extent of decrease is different in different directions.