Coal Pitch Research Articles

Preparation of pitch semi-coke water slurry and its properties of slurryability and gasification

ABSTRACT A new strategy for the preparation of pitch semi-coke water slurry (p-SCWS) with pitch as raw material and semi-coke powder was proposed. The slurryability and gasification performance of p-SCWS were evaluated by apparent viscosity, stability, FTIR, XRD, and TG/DTG characterization methods. Compared with SCWS, the hydrophilic functional groups of SCWS prepared by coal pitch (CP), modified pitch (MP), and petroleum pitch (PP) increased significantly. p-SCWS and SCWS have similar pseudoplastic rheological properties-shear thinning. p-SCWS exhibits better stability than SCWS, with the lowest WSR at 0% and the highest at 8.49%. The addition of pitch lowered the initial (Ts) and final reaction temperatures (Te) of gasification, increased the activation energy and pre-exponential factor, and enhanced the gasification activity. The Ts and Te of CP-SCWS showed the most significant decrease, reaching 869.95°C and 1010.96°C, respectively, compared to 902.39°C and 1075.60°C for SCWS. The activation energy and pre-exponential factor were highest for PP-SCWS.

Construction of Low‐Softening‐Point Coal Pitch Derived Carbon Nanofiber Films as Self‐Standing Anodes Toward Sodium Dual‐Ion Batteries

AbstractTo achieve high‐quality hard carbon nanofibers (HCNFs), and particularly flexible HCNFs films is the eternal pursuit from low‐cost coal pitch (CP). However, it is still trapped seriously by the inborn bottleneck of low‐softening‐point (LSP) characteristics of CP itself. Herein, an efficient Bi(NO3)3·5H2O‐assisted electrospinning‐carbonization methodology is creatively devised to obtain flexible HCNFs films directly from LSP CP. The essential roles of Bi(NO3)3·5H2O and pre‐oxidation in constructing flexible films are rationally proposed. With further regulation in Bi(NO3)3·5H2O dosage and calcination temperatures, specific micro‐structures/morphologies of flexible HCNFs films are finely optimized. The optimum HCNFs‐1.2 film is endowed with robust structural flexibility/stability, high‐content active oxygen/nitrogen groups, abundant graphic microcrystalline zones of large interlayer spacing, and convenient ion‐diffusion channels. Thanks to such remarkable merits, HCNFs‐1.2 retains a large reversible capacity of 125.3 mAh g‒1 over 1000 cycles at 1.0 A g‒1, when evaluated as a self‐supporting film anode for sodium dual‐ion batteries (SDIBs). Furthermore, the HCNFs‐1.2‐based SDIBs deliver a specific capacity of 90.9 mAh g‒1 at 0.1 A g‒1, along with a capacity retention of 78.4% after 1500 cycles at 1.0 A g‒1. The insightful understanding here will provide meaningful guidance for rational design of advanced flexible film electrodes toward next‐generation SDIBs and beyond.

N-Doped Porous Carbon Based on Anion and Cation Storage Chemistry for High-Energy and Power-Density Zinc Ion Capacitor.

Zinc ion hybrid capacitors (ZIHCs) show promise for large-scale energy storage because of their low cost, highly intrinsic safety, and eco-friendliness. However, their energy density has been limited by the lack of advanced cathodes. Herein, a high-capacity cathode material named N-doped porous carbon (CFeN-2) is introduced for ZIHCs. CFeN-2, synthesized through the annealing of coal pitch with FeCl3·6H2O as a catalytic activator and melamine as a nitrogen source, exhibits significant N content (10.95 wt%), a large surface area (1037.66 m2 g-1), abundant lattice defects and ultrahigh microporosity. These characteristics, validated through theoretical simulations and experimental tests, enable a dual-ion energy storage mechanism involving Zn2+ ions and CF3SO3 - anions for CFeN-2. When used as a cathode in ZIHCs, CFeN-2 achieves a high-energy density of 142.5W h kg-1 and a high-power density of 9500.1W kg-1. Furthermore, using CFeN-2 ZIHCs demonstrate exceptional performance with 77% capacity retention and nearly 100% coulombic efficiency after 10 000 cycles at 10 A g-1, showcasing substantially superior performance to current ZIHCs. This study offers a pathway for developing high-energy and high-power cathodes derived from coal pitch carbon for ZIHC applications.

Control of Thermochemical Transformations of Components of Coal-Based Binders

The possibility of considering coal pitch as a material suitable for research modeling the processes of thermochemical transformations of the plastic mass of coal carbonization and their interaction with the solid carbon phase is analyzed. The possibilities of controlling the properties of coal pitch and blast furnace coke during its production with the help of aprotic acid additives in the presence of a co-catalyst are shown.

Impregnation of Graphite with Aluminum under High Pressure

To impregnate graphite of the GMZ brand with liquid aluminum alloy D16, a high-pressure method and apparatus previously used for impregnating carbon frames with liquid coal pitch in the isostatic technology for the production of carbon-carbon composite materials were used. The graphite blank and the amount of aluminum alloy calculated from the initial porosity of graphite were placed in a thin-walled container, degassed in a vacuum furnace, after which the container with the contents was sealed. Thermobaric treatment was carried out at a temperature of 750°C and pressure of 100 and 200 MPa. After finishing the treatment, the density and porosity of the obtained metallographic composites, as well as their compressive strength, were determined. As a result of these thermobaric treatments, the density and compressive strength of the obtained composites increased significantly, and the porosity decreased markedly.

Mechanism of coal pitch pre-hydrogenation catalyzed by metal-free catalytic system and preparation of mesophase pitch

Coal pitch (CP) molecules have high aromaticity, planarity and condensation degree, usually requiring hydrogenation to prepare high-quality mesophase pitch (MP). However, current hydrogenation methods often face challenges such as harsh conditions, residual ash or insufficient hydrogenation. Here, with 5 wt% tetrahydronaphthalene (THN) as the hydrogen donor, hydrogenated CP (HCP) with low ash content and high H/C was prepared at low temperature and pressure via a metal-free catalytic system with boron trifluoride ether (BF3·Et2O) as catalyst and p-toluenesulfonic acid (TsOH) as co-catalyst and 5 wt%. Subsequently, MP was prepared from the HCP, and the mechanisms of catalytic hydrogenation and the formation of mesophase macromolecules were elucidated. The characterization results indicated that CP achieved optimal hydrogenation when the molar ratio of BF3 to TsOH was 1:1. The HCP obtained under this condition can further prepare a wide-area streamlined MP. During the hydrogenation process, TsOH provided proton hydrogen to BF3, forming a complex acid that facilitated carbocation reactions between THN and CP molecules, thereby enhancing hydrogenation efficiency. However, when the molar amount of TsOH exceeded that of BF3, it would catalyze the polymerization of HCP molecules to a certain extent, reducing the hydrogenation effect. Meanwhile, it could introduce more sulfonic acid groups into the molecular structure, causing cross-linking of polycyclic aromatic hydrocarbons and excessive system viscosity during the preparation of the MP, resulting in a mosaic optical texture. This work is of significant importance for promoting the efficient hydrogenation of CP and the preparation of high-quality MP.

Facile construction of porous carbon fibers from coal pitch for Li-S batteries

Coal pitch, an important by-product in the coal coking industry with a high output, is a low-cost and high-carbon yield precursor for the manufacturing of high-value carbon materials. Herein, N/O co-doped carbon fiber (CFCP), fabricated by electrospinning using pre-oxidized coal pitch as the precursor, was employed as the sulfur host for Li-S batteries. The presence of more pyrrolic N and graphic N in CFCP than carbon fiber made from polyacrylonitrile benefits the adsorption of lithium polysulfide and the battery’s life. Sulphur-CFCP cathode (S@CFCP) exhibited excellent specific capacity and cyclability, with a specific capacity of 701.1 mAh/g and a low capacity decay rate of 0.088% per cycle over 200 cycles at 2.0 C, respectively. The high ion diffusion rate, low charge transfer resistance, and effective conversion of lithium polysulfides enable the high electrochemical performance of S@CFCP.

Hierarchical porous carbon originated from the directing associated with activation as high-performance electrodes for supercapacitor and Li ion capacitor

A template-directing methodology combined with post-activation methodology is developed to synthesize hierarchical porous carbon (HPC) with a unique nanocage-like morphology and exceptional structural integrity, utilizing light MgO nanocapsules as templates and coal pitch as precursor. The specific surface area and pore volume of HPC can be precisely adjusted by varying the mass ratio between the chemical activator and PC. This optimized pore structure significantly enhances the kinetics of electrolyte ion diffusion, which is a crucial point for the high-performance supercapacitors. The superior capacitive energy-storage behavior with respect to capacitance and rate capability (168 and 160 F g−1 at 1 and 100 A g−1) can be delivered by HPC electrode as compared to commercial activated carbon and pristine PC. The great compatibility to high gravimetric and areal capacitances (173 F g−1 and 1391 mF cm−2) can still be achieved even at 8 mg cm−2 for HPC electrode. Moreover, a full hybrid Li ion capacitor fabricated using HPC, delivers outstanding rate capability, excellent Ragone performance, and exceptional cyclability, establishing the potential of this material for advanced energy storage systems. The successful integration of template-directed synthesis with activation techniques presents a scalable approach to convert coal pitch into high-performance electrode materials.

Excellent capacitive storage performance of N-doped porous carbon derived from the orientation-guidance coupled with in-situ activation methodology

The orientation-guidance coupled with in-situ activation methodology is developed to synthesize the N-doped porous carbon (NPC) with well-developed porosity and high specific surface area, using coal pitch as a carbon precursor. The orientation-guidance and activation are dedicated to generating microporous and mesoporous channels, respectively. The in-situ N incorporation into the carbon skeleton is realized along with the formation of porous carbon (PC), ensuring the uniformity of N doping. As an electrode material of supercapacitor, benefiting from the robust hexagon-like building block decorated with micro-mesoporous channels and N doping, NPC electrode affords a significant improvement in capacitive energy-storage performance, achieving a specific capacitance of up to 333F g−1 at 1 A/g, which far exceeds those of PC and activated carbon. Notably, even under high mass loading of 10 mg cm−2, the NPC maintains a satisfactory capacitance of 258F g−1 at 1 A/g. When employed as the anode in Li-ion capacitor (LIC), apart from exhibiting enhanced anode behavior compared to graphite anode, NPC also delivers exceptional cyclability. Furthermore, density functional theory calculations have validated the enhanced electrical conductivity and Li storage ability contributed by N doping, providing a theoretical foundation for the observed improvements in electrochemical performance. A full LIC configured with NPC anode delivers extraordinary Ragone performance and outstanding cyclability. This work also proposes a feasible way to realize the oriented conversion of coal pitch into high-performance electrode materials for electrochemical energy-storage devices.

Mesophase pitch-based high performance carbon fiber production using coal extracts from mild direct coal liquefaction

Mild direct coal liquefaction (autogenous pressure, no catalyst, no H2 gas) of Springfield coal in fluid catalytic cracking decant oil is shown to effectively produce coal extract precursors to spinnable mesophase pitch. This work demonstrates that the coal extract can be thermally treated to obtain mesophase pitch in a facile one-step process, bypassing the production of an intermediate isotropic pitch. Furthermore, the presence of 25 wt.% coal in the initial slurry can increase the yield to mesophase pitch nearly twofold and yield to carbon fiber by approximately 70%. The coal extract-derived mesophase pitch was melt-spun and heat treated to produce carbon fiber with graphitic texture, high modulus (>400 GPa) and tensile strength up to 943 MPa. Overall, this work demonstrates that coal can be effectively utilized to markedly amplify the mesophase pitch and carbon fiber yield from fluid catalytic cracking decant oil by relatively simple processing, while conserving utility as a precursor to high performance carbon fiber and potentially other high value graphitic products.

Effect of isopropyl chloride addition in AlCl3 catalytic system on the formation of coal tar pitch-based mesophases

Mesophase pitch is a high-quality precursor for the synthesis of high-performance pitch-based carbon fibers. The mesophase content, texture and softening point are the most important factors for the structure, properties and spinnability of mesophase pitch (MP). Herein, we report a novel approach for the preparation of mesophase pitch with high anisotropic content and low softening point by AlCl3 catalytic pyrolysis in the presence of isopropyl chloride (PrCl). The variation of anisotropic content and mesophase texture under different PrCl additions and the effect of the introduction of isopropyl on the molecular stacking of aromatic lamellar molecules were investigated. The results confirmed that, except for their role in improving catalytic activity, carbocation co-catalysts can improve the structure and molecular assembly of aromatic molecules through the introduction of alkyl groups. The reaction of isopropyl chloride (PrCl) as a co-catalyst catalyzed pyrolysis of medium-temperature coal pitch at 370 ℃ for 8 h produced a bulk mesophase with a content close to 100 %. Compared to the AlCl3 system (without PrCl), the AlCl3-PrCl system can catalyze the preparation of mesophases at lower temperatures. In addition, it is logical that the introduction of isopropyl group significantly increases the stacking spacing of the mesophase pitch layer molecules, which can effectively improve the mobility of the aromatic layer molecules resulting in the growth of mesophase. The fusion texture and anisotropic content of mesophase pitch were significantly improved by replacing the nucleophilic reagent of the AlCl3-catalyzed system. This work provides feasible ideas for the preparation of high-performance coal tar based mesophase pitch.

Construction of coal pitch-based HA-K grafted poly condensates and their excellent anti-temperature and viscosity-reducing properties

Humic acids (HAs) are widely used as filtrate and viscosity reducers in drilling fluids. However, their practical utility is limited due to poor stability in salt resistance and high-temperature resistance. High-temperature coal pitch (CP) is a by-product from coal pyrolysis above 650 °C. The substance's molecular structure is characterized by a dense arrangement of aromatic hydrocarbon and alkyl substituents. This unique structure gives it unique chemical properties and excellent drilling performance, surpassing traditional humic acids in drilling operations. Potassium humate is prepared from CP (CP-HA-K) by thermal catalysis. A new type of high-quality humic acid temperature-resistant viscosity-reducer (Graft CP-HA-K polymer) is synthesized with CP-HA-K, hydrolyzed polyacrylonitrile sodium salt (Na-HPAN), urea, formaldehyde, phenol and acrylamide (AAM) as raw materials. The experimental results demonstrate that the most favorable conditions for the catalytic preparation of CP-HA-K are 1 wt% catalyst dosage, 30 wt% KOH dosage, a reaction temperature of 250 °C, and a reaction time of 2 h, resulting in a maximum yield of CP-HA-K of 39.58%. The temperature resistance of the Graft CP-HA-K polymer is measured to be 177.39 °C, which is 55.39 °C higher than that of commercial HA-K. This is due to the abundant presence of amide, hydroxyl, and amine functional groups in the Graft CP-HA-K polymer, which increase the length of the carbon chains, enhance the electrostatic repulsion on the surface of solid particles. After being aged to 120 °C for a specified duration, the Graft CP-HA-K polymer demonstrates significantly higher viscosity reduction (42.12%) compared to commercial HA-K (C-HA-K). Furthermore, the Graft CP-HA-K polymer can tolerate a high salt concentration of 8000 mg·L−1, measured after the addition of optimum amount of 3 wt% Graft CP-HA-K polymer. The action mechanism of Graft CP-HA-K polymer on high-temperature drilling fluid is that the Graft CP-HA-K polymer can increase the repulsive force between solid particles and disrupt bentonite's reticulation structure. Overall, this research provides novelty insights into the synthesis of artificial humic acid materials and the development of temperature-resistant viscosity reducers, offering a new avenue for the utilization of CP resources.

Study on the characterization and thermal conversion behavior of sequential extraction products from medium temperature coal pitch

To achieve the high value-added clean utilization of medium temperature coal pitch (MTP), five fractions were separated from MTP by the sequential extraction method using n-heptane, n-butanol, toluene, tetrahydrofuran and quinoline as solvents. Briefly, the extracts were analysed using proximate analysis, elemental analysis, fourier infrared spectrum (FTIR), ultraviolet visible spectrum (UV–vis), fluorescence spectrum, and thermogravimetric analysis (TGA) to investigate their structural parameters, aromatic condensation degree and pyrolysis properties. Meanwhile, Raman spectrum, X-ray diffraction (XRD), and polarizing microscope were used to quantitatively analyze the microstructures of thermal conversion products of the extracts. This allowed for investigation of the thermal conversion mechanism and determination of the thermal conversion behavior. In fact, the chain index (CH3/CH2), aromatic index (Iar), aromatic condensation degree and thermal stability of the extracts increase gradually with deeper extraction. Extracts with high aromatic condensation degree are more favorable for the formation of mesocarbon microbeads (MCMBs). However, overly aromatic condensation degree will lead to excessive coalescence of MCMBs. The ideal carbon microcrystalline content increases with higher temperatures during the thermal conversion of the same fraction. But the change of amorphous carbon content has no obvious regularity. The results of this work will provide theoretical and experimental support for the selection of precursors for carbon/graphite materials.

Polymer Composites with Carbon Fillers Based on Coal Pitch and Petroleum Pitch Cokes: Structure, Electrical, Thermal, and Mechanical Properties.

The effect of particle size and oxidation degree of new carbon microfillers, based on coal pitch (CP) and petroleum pitch (PET) cokes, on the structure as well as thermal, mechanical, and electrical properties of the composites based on ultrahigh molecular weight polyethylene (UHMWPE) was investigated. The composites studied have a segregated structure of filler particle distribution in the UHMWPE matrix. It was found that composite with smaller CP grain fraction has the highest Young's modulus and electrical conductivity compared to the other composites studied, which can be the result of a large contribution of flake-shaped particles. Additionally, conductivity of this composite turned out to be similar to composites with well-known carbon nanofillers, such as graphene, carbon black, and CNTs. Additionally, the relationship between electrical conductivity and Young's modulus values of composites studied was revealed, which indicates that electrical conductivity is very sensitive to the structure of the filler phase in the polymer matrix. In general, it was established that the properties, especially the electrical conductivity, of the composites studied strongly depends on the size, shape, and oxidative treatment of CP and PET filler particles, and that the CP coke of appropriately small particle sizes and flake shape has significant potential as a conductive filler for polymer composites.

Preparation of layered porous carbon supported ruthenium catalyst and its performance for ammonia borane hydrolyzing to hydrogen

In this paper, layered porous carbon sheet (LPCS) was obtained through high temperature calcination under argon atmosphere by using coal pitch as carbon material, sodium chloride as template agent and potassium carbonate as activator. Then, the active component Ru was loaded onto the LPCS support by impregnation to synthesize Ru/LPCS catalyst whose catalytic performance for hydrogen production by hydrolysis of ammonia borane was studied. The results showed that in the presence of light, the maximum value of the turnover frequency (TOF), 334.8 min–1, was obtained at a calcination temperature of 1123 K and a loading of 2% of Ru which is 1.38 times higher than that in the absence of light. The activation energy (Ea) of the catalyst decreased from 90.60 to 70.33 kJ/mol in the presence of light. The hydrogen production rate order with respect to ammonia borane concentration was 0.75, which is first-order relation to the amount of the catalyst.

Experimental and theoretical insight into the effect of a novel composite dispersant on the properties of coal pitch water slurry

To optimize the utilization efficiency of coal pitch (CP), an innovative composite dispersant was designed and employed in the preparation of coal pitch water slurry (CPWS) by effectively combining modified sodium lignosulfonate (MLS) and amphoteric polycarboxylate (AAD) based on the principle of complementary advantages. The effects of the proportion of MLS to AAD on the characteristics of CPWS were systematically analyzed and assessed by various technical methods, including apparent viscosity, rheological behavior, static stability, adsorption behavior, etc. Results indicated that the CPWSs utilizing distinct composite dispersants belonged to the category of yield pseudoplastic fluids and had a good correlation with the Herschel-Bulkley model. Among them, the CD-2, composite dispersant with a mass ratio of MLS:AAD = 1:1, exhibited superior performance in terms of viscosity reduction and stabilization properties. It demonstrated the maximum adsorption capacity (5.23 mg/g) and adsorption layer thickness (7.22 nm) compared to other dispersants. Meanwhile, it could significantly increase the wettability (with a contact angle of 74.5°) and the absolute Zeta potential value (32.5 mV) of CP. The density functional theory (DFT), molecular dynamics (MD) simulation, and extended Derjaguin-Landua-Verwey-Overbeek (eDLVO) theory were carried out to investigate the interaction mechanism of composite dispersant with CP and the interaction energy among CP particles. The differences in energy levels between the lowest unoccupied molecular orbital (LUMO) and the highest occupied molecular orbital (HUMO) of MLS and AAD were significantly smaller than that of H2O. The hydrophobic groups of composite dispersants were efficiently adsorbed onto CP, while the hydrophilic groups adsorbed water molecules, with an adsorption energy reaching −169.36 kcal/mol. The steric hindrance of composite dispersant exerted a crucial influence on the dispersion of CPWS, enabling CP particles to be stabilized in water. The present study offers a novel approach to enhance the characteristics of CPWS and establishes a theoretical foundation for the design of efficient composite dispersants.

The Microstructure and Thermal Conductive Behavior of Three-Dimensional Carbon/Carbon Composites with Ultrahigh Thermal Conductivity.

Carbon-based composite materials, denoted as C/C composites and possessing high thermal conductivity, were synthesized utilizing a three-dimensional (3D) preform methodology. This involved the orthogonal weaving of mesophase pitch-based fibers in an X (Y) direction derived from low-temperature carbonization, and commercial PAN-based carbon fibers in a Z direction. The 3D preforms were saturated with mesophase pitch in their raw state through a hot-pressing process, which was executed under relatively low pressure at a predetermined temperature. Further densification was achieved by successive stages of mesophase pitch impregnation (MPI), followed by impregnation with coal pitch under high pressure (IPI). The microstructure and thermal conductivity of the C/C composites were systematically examined using a suite of analytical techniques, including Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD), and PLM, amongst others. The findings suggest that the volumetric fraction of fibers and the directional alignment of the mesophase pitch molecules can be enhanced via hot pressing. The high graphitization degree of the mesophase pitch matrix results in an increased microcrystalline size and thus improved thermal conductivity of the C/C composite. Conversely, the orientation of the medium-temperature coal pitch matrix is relatively low, which compensates for the structural inadequacies of the composite material, albeit contributing minimally to the thermal conductivity of the resultant C/C composites. Following several stages of impregnation with mesophase pitch and subsequent impregnation with medium-temperature coal pitch, the 3D C/C composites yielded a density of 1.83 and 2.02 g/cm3. The thermal conductivity in the X (Y) direction was found to be 358 and 400 W/(m·K), respectively.

Construction of the N, S co-doped C/FeS2 materials for low thickness and high-efficiency microwave absorption

Research into electromagnetic wave-absorbing materials is essential to tackle the growing impact of electromagnetic wave pollution on human health and social advancement. Therefore, a method for synthesizing N,S co-doped C/FeS2 porous carbon composite absorbers (N,S@APCs) with low thickness, low filler content, and high performance is reported. The porous carbon structures were prepared by a high-temperature-hydrothermal two-step method using directly liquefied coal pitch as the carbon source. The successful doping of diatomic N and S at optimal concentrations enhances their impedance matching capacity. At the same time, forming FeS2 through the reaction between S and Fe3+ in the raw material efficiently improves the dielectric loss effect and enhances interfacial and dipole polarization effects. These factors together contribute to the strong absorption performance and low matching thickness of the fabricated N, S@APCs. At a thickness of 1.5 mm, 10 wt% of absorber filling resulted in a strong absorption performance with RLmin=-51.05 dB. Meanwhile, at a thickness of 1.7 mm, an effective absorption bandwidth of 4.76 GHz was achieved. This research offers a novel viewpoint on investigating porous carbon absorbers at low thicknesses. It serves as a reference for later investigations into polyatomic co-doped porous carbon absorbers.

RESEARCHES OF THERMO-OXIDATIVE TREATMENT OF ELECTRODE COAL PITCH

RESEARCHES OF THERMO-OXIDATIVE TREATMENT OF ELECTRODE COAL PITCH

Modification of the properties of coal electrode pitch

We considered the use of electrode pitch as a binding material and the ways of processing it in order to improve its operational properties as an electrode material. The existing methods of modifying electrode pitches do not sufficiently ensure the formation of the properties of electrode masses and, accordingly, the operational characteristics of self-igniting electrodes. Therefore, in this research, a technological method was developed aimed at improving these properties by modifying it with a surface-active substance. The modification with a surface-active substance made it possible to establish the structural and chemical modification of the electrode masses by evaluating, based on the structural changes, the main characteristics and physicochemical properties that determine their behavior in the process of carbonization of the working end of the self-igniting electrode. Phenol-formaldehyde resin was used as a surfactant. The results of the study showed that the use of phenol-formaldehyde resin as a modifier of electrode pitch allowed reducing the specific electrical resistance of carbon masses by 11% and increasing the tensile strength limits by 9% due to the change in diffusion properties in the "filler–binder" system. It was established that the modifier contributes to the intensification of the processes of association of supramolecular substances (graphitosomes); the relationship between the rheological parameters and the rational composition of the polydisperse system of organic pitch mass was revealed. It was proposed to add a modifier of up to 2% at the expense of medium-temperature pitch B1 in the composition of carbon masses. This made it possible to reduce the use of medium-temperature pitch, improve the operational properties of carbon graphite products and reduce the burden on the environment.