High-temperature Carbonization Research Articles

In Situ Self-Assembly of Nitrogen-Doped 3D Flower-like Hierarchical Porous Carbon and Its Application for Supercapacitors

The hierarchical porous carbon-based materials derived from biomass are beneficial for the enhancement of electrochemical performances in supercapacitors. Herein, we report the fabrication of nitrogen-doped 3D flower-like hierarchical porous carbon (NPC) assembled by nanosheets using a mixture of urea, ZnCl2, and starch via a low-temperature hydrothermal reaction and high-temperature carbonization process. As a consequence, the optimized mass ratio for the mixture is 2:2:2 and the temperature is 700 °C. The NPC structures are capable of electron transport and ion diffusion owing to their high specific surface area (1498.4 m2 g−1) and rich heteroatoms. Thereby, the resultant NPC electrodes display excellent capacitive performance, with a high specific capacitance of 249.7 F g−1 at 1.0 A g−1 and good cycling stability. Remarkably, this implies a superior energy density of 42.98 Wh kg−1 with a power density of 7500 W kg−1 in organic electrolyte for the symmetrical supercapacitor. This result verifies the good performance of as-synthesized carbon materials in capacitive energy storage applications, which is inseparable from the hierarchical porous features of the materials.

In Situ Construction of CdS/g-C3N4 Heterojunctions in Spent Thiolation@Wood-Aerogel for Efficient Excitation Peroxymonosulfate to Degradation Tetracycline.

Pollutant treatment, hazardous solid waste conversion, and biomass resource utilization are significant topics in environmental pollution control, and simultaneously achieving them is challenging. Herein, we developed a "from waste absorbent to effective photocatalyst" upcycle strategy for nontoxic conversion of Cd(II) adsorbed on thiolation@wood-aerogel (TWA) into CdS/g-C3N4 heterojunctions through the in situ chemical deposition high-temperature carbonization combined conversion method to overcome the above problems simultaneously. We used Schiff base reaction to graft l-cysteine into dialdehyde@wood-aerogel to prepare TWA with a high Cd(II) adsorption capacity (600 mg/L, 294.66 mg/g). Subsequently, the spent Cd(II)-loaded-TWA was used as a substrate for in situ construction of Cd(II) into CdS/g-C3N4 heterojunction for activating peroxymonosulfate (PMS) under simulated sunlight [simulated solar light (SSL)], achieving efficient tetracycline (TC) degradation (20 mg/L, 95.32%). The Langmuir and pseudo-second-order models indicate single-layer chemical adsorption of Cd(II) on the TWA adsorption process. In the PMS/SSL system, CdS/g-C3N4@TWA efficiently and rapidly degraded TC via an adsorption-photocatalytic synergistic degradation mechanism. The used CdS/g-C3N4@TWA has a good biocompatibility. This study proposed design and preparation of a new type of wood aerogel absorbent and provided a novel upcycling strategy for innovative use of the spent waste adsorbent.

Core–Double-Shell TiO2@Fe3O4@C Microspheres with Enhanced Cycling Performance as Anode Materials for Lithium-Ion Batteries

Due to the volume expansion effect during charge and discharge processes, the application of transition metal oxide anode materials in lithium-ion batteries is limited. Composite materials and carbon coating are often considered feasible improvement methods. In this study, three types of TiO2@Fe3O4@C microspheres with a core–double-shell structure, namely TFCS (TiO2@Fe3O4@C with 0.0119 g PVP), TFCM (TiO2@Fe3O4@C with 0.0238 g PVP), and TFCL (TiO2@Fe3O4@C with 0.0476 g PVP), were prepared using PVP (polyvinylpyrrolidone) as the carbon source through homogeneous precipitation and high-temperature carbonization methods. After 500 cycles at a current density of 2 C, the specific capacities of these three microspheres are all higher than that of TiO2@Fe2O3 with significantly improved cycling stability. Among them, TFCM exhibits the highest specific capacity of 328.3 mAh·g−1, which was attributed to the amorphous carbon layer effectively mitigating the capacity decay caused by the volume expansion of iron oxide during charge and discharge processes. Additionally, the carbon coating layer enhances the electrical conductivity of the TiO2@Fe3O4@C materials, thereby improving their rate performance. Within the range of 100 to 1600 mA·g−1, the capacity retention rates for TiO2@Fe2O3, TFCS, TFCM, and TFCL are 27.2%, 35.2%, 35.9%, and 36.9%, respectively. This study provides insights into the development of new lithium-ion battery anode materials based on Ti and Fe oxides with the abundance and environmental friendliness of iron, titanium, and carbon resources in TiO2@Fe3O4@C microsphere anode materials, making this strategy potentially applicable.

Bimetallic-doped three-dimensional carbon skeleton porous material as efficient catalysts for oxygen reduction reaction

The slowness of the oxygen reduction reaction (ORR) kinetics of the fuel cell cathode has terrifically inhibited its development process. Now it is of considerable importance to research low-cost, multi-defect, high-performance non-noble metal ORR catalysts. Specifically, CuO nanosheets are grown in situ on ZIF-8 to form a composite material (zif-8@CuO), and then undergo a high-temperature carbonization process. Finally, the Zn-Cu codoped composite material Zn-xCu-N/C with a porous structure supported by a three-dimensional carbon skeleton can be obtained. The material has a 3D carbon skeleton support and a rich pore structure, which can expose more active sites. The combination of bimetallic Zn and Cu with carbon materials also increases the overall stability and conductivity of the material, which is beneficial to improvement of catalytic performance. The electrochemical performance test results show that the onset potential and half-wave potential of the Zn-0.1Cu-N/C material are 0.889 V and 0.803 V respectively, with a low Tafel slope of 62 mV dec−1 and excellent long-term stability. After 10000 cycles, the ORR curve only changed 18 mV, while the carbon skeleton can still maintain unchanged.

Synthesis and Catalytic Performance of Mo2C/MoS2 Composite Heterojunction Catalysts.

Hydrogen, as a clean, safe, and efficient energy carrier, is one of the hot energy sources that have attracted much attention. Mo2C, due to the introduction of C atoms, makes the atomic spacing of the Mo lattice decrease and changes the width of the d-band, which makes the electronic properties of Mo2C similar to that of Pt noble metals, exhibiting excellent electrochemical hydrogen precipitation performance. MoS2, due to its special crystal structure and tunable electronic structure, has been widely studied. In this paper, Mo2C nanoparticles were prepared by high-temperature carbonization, and then two-dimensional layered MoS2 were be loaded on Mo2C nanoparticles by the hydrothermal method to synthesize Mo2C/MoS2 composite catalysts. Their electrochemical hydrogen precipitation (HER) performance under acidic conditions was tested. The above catalysts were also characterized by modern material testing methods such as XRD, SEM, TEM, and XPS. The results showed that the composite catalysts exhibited the most excellent electrochemical hydrogen precipitation performance at Mo2C/MoS2-3, with the lowest overpotential at a current density of 10 mA cm-2, Tafel slope, and electrochemical impedance. At the same time, the electrochemically active area was dramatically enhanced, with good stability under prolonged testing. The catalytic activity was significantly improved compared with that of Mo2C and MoS2. The characterization and experimental results indicate that the heterogeneous structure of Mo2C and MoS2 formed a built-in electric field between the two, which accelerated the electron transfer efficiency and provided more active sites. The Mo2C/MoS2 composite catalyst is a low-cost, easy-to-prepare, and high-efficiency electrochemical hydrogen precipitation catalyst, providing a new idea for developing green and clean energy.

Boosting Molecular Cross-Linking in a Phenolic Resin for Spherical Hard Carbon with Enriched Closed Pores toward Enhanced Sodium Storage Ability.

Phenolic resin (PF) is considered a promising precursor of hard carbon (HC) for advanced-performance anodes in sodium-ion batteries (SIBs) because of its facile designability and high residual carbon yield. However, understanding how the structure of PF precursors influences sodium storage in their derived HC remains a significant challenge. Herein, the microstructure of HC is controlled by the degree of cross-linking of resorcinol-benzaldehyde (RB) resin. We reveal that robust molecular cross-linking in RB resin induced by hydrothermal treatment promotes closed-pore formation in the derived HC. The mechanism is devised for the decomposition of a highly cross-linked RB three-dimensional network into randomly stacked short-range graphitic microcrystals during high-temperature carbonization, contributing to the abundant closed pores in the derived HC. In addition, the high cross-linking degree of RB resin endows its derived HC with a small-sized spherical morphology and large interlayer spacing, which improves the rate performance of HC. Consequently, the optimized hydrothermal treatment HC anode shows a higher specific capacity of 372.7 mAh g-1 and better rate performance than the HC anode without hydrothermal treatment (276.0 mAh g-1). This strategy can provide feasible molecular cross-linking engineering for the development of closed pores in PF-based HC toward enhanced sodium storage.

Characteristics of Fe/C catalysts based on pyrolysis of ferric citrate and its peroxymonosulfate activation performance to degrade sulfadiazine in water.

Advanced oxidation techniques based on peroxysulfate activation have been paid much attention owing to their excellent performance in degrading stubborn pollutants in water. In response to the current situation that requires more raw materials and higher costs and involves more complicated processes for the preparation of Fe/C catalysts to activate persulfates, novel catalysts (Fe/C-700, Fe/C-800, Fe/C-900 and Fe/C-1000) were prepared by a high-temperature carbonization method at different pyrolysis temperatures (700, 800, 900 and 1000 °C) using inexpensive and environmentally friendly ferric citrate as raw material. Fe/C catalysts were characterized using SEM, EDS, XRD, XPS, and VSM and were screened for the activation of peroxymonosulfate (PMS) to degrade sulfadiazine (SDZ) in water, where Fe/C-900 exhibited higher efficiency. Thus, its activation performance for PMS to degrade SDZ was comprehensively investigated and the mechanisms of activation degradation were analyzed. The results showed that the degradation rate of 98.7% can be achieved to 10 mg L-1 SDZ by 0.1 g L-1 Fe/C-900 and 0.5 mmol L-1 PMS within 60 min. A wide range of solution pH, low catalyst dosage and good recycling performance were found in the Fe/C-900 application and the amount of iron ions dissolved at the end of the reaction was low (0.350 mg L-1). It was shown that both free radical and non-free radical pathways existed in the reaction system, where 1O2, SO4-˙ and O2-˙ played dominant roles in the degradation process of SDZ. The results could provide new ideas for the preparation of Fe/C catalysts and their heterogeneous activation for PMS to degrade stubborn organic pollutants in water.

Polyoxometalate coupled polymers induced molybdenum phosphide with large surface area for efficient hydrogen evolution

Developing highly active hydrogen evolution reaction (HER) electrocatalysts possesses great significance for the green renewable energy conversion and storage. Here, through the electrostatic attraction between polyoxometalate (PMo12) and ammonium polyphosphate (APP) and the coordination with polyallylamine hydrochloride (PAH), the precursor was constructed, and then nitrogen-doped graphite carbon layer-coated MoP active particles (MoP@NC) were successfully prepared by high temperature carbonization. For HER, the overpotential of η10 for MoP@NC is 119 and 126 mV in acidic and alkaline electrolyte. Furthermore, in alkaline solution, when the current density reaches a certain degree (≥110 mA cm−2), the hydrogen production activity of the catalysts are the same as that of the industrial Pt/C catalysts, or even have a slight advantage. The synergistic interaction of active particles (MoP) and graphitic carbon layers and high specific surface area ensure the excellent activity of HER. N-doped porous carbon layers also protect MoP@NC working for 24 h. Moreover, the catalysts prepared in the same experimental environment with ammonium molybdate as metal source also showed good HER performance in acidic and alkaline environments. This study opens a general way to develop earth-rich Mo-based phosphide electrocatalysts with high activity for hydrolysis applications.

Hexagonal boron nitride-doped carbon membrane as anode for the enhanced adsorption and electrochemical oxidation of phenol

An activated carbon membrane (ACM) doped with hexagonal boron nitride (h-BN) was fabricated by using activated carbon as the raw material and phenolic resin as the binder. The preparation process involves blending raw materials, ball milling, membrane pressing, and high-temperature carbonization. The conductive ACM was employed as an anode to constitute an electrochemical membrane reactor (EMR) for phenol removal. The effect of h-BN doping rate (0–5wt.%) on the properties of ACM was explored. Results showed that ACM1 (1wt.% h-BN) displayed a small pore size (20nm), high porosity (41.6%), large specific surface area (446.8 m2/g), and strong mechanical strength (15.4MPa) compared to the pristine ACM0. The oxygen precipitation potential of ACM1 (2.11V) was much higher than that of ACM0 (1.53V), thus reducing oxygen generation at the anode in EMR for phenol degradation. The phenol removal rate of phenol obtained from EMR with ACM1 as the anode at 1.5V was up to 95.6%, which was much higher than that for ACM0 (39.3%). Density functional theory (DFT) calculations and experimental results confirmed that h-BN-doping enhanced the adsorption active sites, and adsorption energy, leading to the high performance of EMR for phenol removal. In addition, the equilibrium adsorption capacity of ACM1 (10.2mg/g) was much higher than that of ACM0 (3.7mg/g). The C atoms adjacent to pyridine N in ACM1 were identified as the adsorption and active catalytic sites by X-ray photoelectron spectroscopy (XPS) and DFT calculations. Therefore, this study sheds light on the design and fabrication of conductive carbon membranes for enhanced performance in industrial wastewater treatment.

Multiscale enhancement of carbon/carbon composite performance by self-assembly of sulfonated graphene with silane-treated carbon fibers

The application prospects of carbon/carbon composites are greatly limited by interfacial cracks and pores caused by binder pitch displacement and cracking during high-temperature carbonization. In this study, silane coupling agent was coated on the surface of oxygen plasma-treated carbon fibers (CFs) and subsequently electrostatically self-assembled with sulfonated graphene (SG) to improve the interfacial bonding between filler and CTP. The results indicate that the tensile strength of carbon fiber treated with silane coupling agent increased by 19 % compared to untreated CF. This increase in strength may be related to the layer of silane coupling agent that repaired the grooves and imperfections on the CF surface. The addition of SG not only improves the distribution characteristics of the fibers, allowing the silane-treated CF to play a greater role in the matrix, but also creates a three-dimensional hydrogen-bonded cross-linking between the SG and the coal tar pitch (CTP) on the surface of the fibers. This inhibits CTP displacement and pyrolysis, achieving a tight bonding of the fiber to the matrix. The composites' structural integrity and mechanical properties were significantly improved due to the synergistic effect of silane-treated CF and SG. The compressive strength was 216.98 MPa, with a flexural strength of 54.78 MPa, 250 % higher than the untreated carbon fiber-reinforced composites. Additionally, the porosity decreased by 31.5 %, and the antioxidant properties increased. The study presents a potential solution to improve the performance of carbon/carbon composites by using the silane-treated CF-SG multiscale reinforced phase.

Nickel-Fe3O4@Graphene coated lightweight carbonized wood for efficient electromagnetic interference shielding

The miniaturization and integration of electronic equipment promote electromagnetic effect radiation pollution more and more serious. The lightweight, renewable electromagnetic interference (EMI) shielding materials is urgently needed. This study developed a high temperature carbonization, Fe3O4@Graphene impregnation, and electroless Ni technique to construct a carbonized wood composite with strong EMI shielding performance using sustainable natural wood as the raw material. The Fe3O4@Graphene is distributed throughout the carbonized wood to provide the conductivity and magnetism of the reinforced composite material, and provide more interfaces to increase the dielectric loss and magnetic loss, thereby exhibiting excellent EMI shielding performance. The results show that at low thickness (2 mm) and ultra-low density (0.284 g/cm3), the CWN-7 composite exhibits excellent EMI shielding effectiveness of up to 84.2 dB in the whole X-band (8.2–12.4 GHz). At the same time, it has extraordinary compressive strength and good thermal insulation performance. This study offers a different method for creating composite multifunctional electromagnetic shields out of carbonized green wood.

The regulatory role of cysteine in active phase construction of polyoxometalate-based hydrodesulfurization catalysts: Reduction, chelation, and dispersion

Polyoxometalate-based hydrodesulfurization (HDS) catalysts were modified using cysteine to construct efficient CoMoS active phase. Cysteine, characterized by chelating (–COOH, –NH2) and reducing (−SH) groups, assumed a triple role in catalyst synthesis, including reduction, chelation, and dispersion. Cysteine pre-reduced polyoxometalates to heteropoly blue, significantly increasing the catalyst sulfidation. The increased nucleophilicity of heteropoly blue enhanced their attraction to Co2+ ions, intensifying the Co-Mo bimetallic synergy. The formation of Co-chelate species delayed Co sulfidation, allowing for the concurrent sulfidation of both Co and Mo species and promoting the generation of the CoMoS active phase. Carbonaceous deposits from the high-temperature carbonization of cysteine weakened the metal-support interaction, facilitating the dispersion of the active phase. The S-CoPMo12-Cys/Al2O3 catalyst demonstrated high activity in the HDS reaction of dibenzothiophene, showcasing their potential for advanced HDS reaction.

Two-phase magnetic nanospheres with magnetic coupling effect encapsulated in porous carbon to achieve lightweight and efficient microwave absorbers

Component selection is crucial for microwave absorbents. Multi-component absorbers are increasingly useful and can be prepared through the rational design and control of various electrical, magnetic, and other auxiliary components. In this paper, Ni3Fe/NiFe2O4 nanospheres with two-phase magnetism were designed for use as a multi-component absorber. Specifically, a Ni3Fe/ NiFe2O4@SPC composite with 3D networks was successfully fabricated by hydrothermal method, high-temperature carbonization for activation, and electrostatic self-assembly. The contact interface and coupling effect between the two magnetic components can promote the attenuation of electromagnetic waves. Moreover, the introduction of porous carbon successfully inhibits the easy aggregation of the magnetic particles. Impressively, with a filling load of 10 wt%, the optimal RL of the prepared Ni3Fe/NiFe2O4@SPC composite reaches −60.6 dB, and the effective absorption bandwidth is 5.2 GHz at 2 mm. The combination of two magnetic components and porous carbon in this multiphase microwave-absorbing composite demonstrates a feasible strategy for designing efficient microwave absorbers in the future.

Fluorinated polymer-derived microporous carbon spheres for CFx cathodes with high energy density

Fluorinated carbon (CFx) compounds have extensive applications in lithium primary battery cathodes owing to their high energy density. In this investigation, a novel CFx compound offering superior electrochemical properties was synthesized via a low-temperature fluorination process, utilizing Pluronic F127 as a template agent and microporous carbon spheres produced through soft template-assisted high-temperature carbonization and chemical activation as precursors, and by regulating the amount of soft template F127 added. The reduction in microsphere size, narrower particle size distribution, and introduction of defects contribute to augmenting the molar ratio of F to C (F/C) of CFx while preserving the electrochemical activity of C-F bonds. The specific capacity of fluorinated polymer-derived microporous carbon spheres (FPMCSs) with a high fluorination degree rivals that of commercial fluorinated graphite (FG). The microsphere morphology and microporous structure not only furnish abundant sites for fluorination reactions in electrode processes but also facilitate Li+ diffusion, ensuring ample rate capability. The synthesized FPMCSs exhibited a peak specific capacity of 1079 mAh g–1 and a maximum energy density of 2679 Wh kg–1 (substantially surpassing the 2180 Wh kg–1 of commercial FG). Hence, the prepared FPMCSs underscore the significance of selecting suitable carbonaceous materials and designing structures deliberately, showing promising potential for achieving high energy density in CFx cathodes in the future, employing readily available and cost-effective raw materials.

Transforming Waste into Wealth: Advanced Carbon-Based Electrodes Derived from Refinery and Coal By-Products for Next-Generation Energy Storage.

This comprehensive review addresses the need for sustainable and efficient energy storage technologies against escalating global energy demand and environmental concerns. It explores the innovative utilization of waste materials from oil refineries and coal processing industries as precursors for carbon-based electrodes in next-generation energy storage systems, including batteries and supercapacitors. These waste-derived carbon materials, such as semi-coke, coal gasification fine ash, coal tar pitch, petroleum coke, and petroleum vacuum residue, offer a promising alternative to conventional electrode materials. They present an optimal balance of high carbon content and enhanced electrochemical properties while promoting environmental sustainability through effectively repurposing waste materials from coal and hydrocarbon industries. This review systematically examines recent advancements in fabricating and applying waste-derived carbon-based electrodes. It delves into the methodologies for converting industrial by-products into high-quality carbon electrodes, with a particular emphasis on carbonization and activation processes tailored to enhance the electrochemical performance of the derived materials. Key findings indicate that while higher carbonization temperatures may impede the development of a porous structure, using KOH as an activating agent has proven effective in developing mesoporous structures conducive to ion transport and storage. Moreover, incorporating heteroatom doping (with elements such as sulfur, potassium, and nitrogen) has shown promise in enhancing surface interactions and facilitating the diffusion process through increased availability of active sites, thereby demonstrating the potential for improved storage capabilities. The electrochemical performance of these waste-derived carbon materials is evaluated across various configurations and electrolytes. Challenges and future directions are identified, highlighting the need for a deeper understanding of the microstructural characteristics that influence electrochemical performance and advocating for interdisciplinary research to achieve precise control over material properties. This review contributes to advancing electrode material technology and promotes environmental sustainability by repurposing industrial waste into valuable resources for energy storage. It underscores the potential of waste-derived carbon materials in sustainably meeting global energy storage demands.

Tailoring the A and B site of Fe-based perovskites for high selectivity in the reverse water-gas shift reaction

The reverse water-gas shift reaction (rWGS) is of particular interest as it is the first step to producing high-added-value products from carbon dioxide (CO2) and renewable hydrogen (H2), such as synthetic fuels or other chemical building blocks (e.g. methanol) through a modified Fischer-Tropsch process. However, side reactions and material deactivation issues, depending on the conditions used, still make it challenging. Efforts have been put into developing and improving scalable catalysts that can deliver high selectivity while at the same time being able to avoid deactivation through high temperature sintering and/or carbon deposition. Here we design a set of perovskite ferrites specifically tailored to the hydrogenation of CO2 via the reverse water-gas shift reaction. We tailor the oxygen vacancies, proven to play a major role in the process, by partially substituting the primary A-site element (Barium, Ba) with Praseodymium (Pr) and Samarium (Sm), and also dope the B-site with a small amount of Nickel (Ni). We also take advantage of the exsolution process and manage to produce highly selective Fe-Ni alloys that suppress the formation of any by-products, leading to up to 100% CO selectivity.

Long-Chain Hydrocarbons from Nonthermal Plasma-Driven Biogas Upcycling.

The burgeoning necessity to discover new methodologies for the synthesis of long-chain hydrocarbons and oxygenates, independent of traditional reliance on high-temperature, high-pressure, and fossil fuel-based carbon, is increasingly urgent. In this context, we introduce a nonthermal plasma-based strategy for the initiation and propagation of long-chain carbon growth from biogas constituents (CO2 and CH4). Utilizing a plasma reactor operating at atmospheric room temperature, our approach facilitates hydrocarbon chain growth up to C40 in the solid state (including oxygenated products), predominantly when CH4 exceeds CO2 in the feedstock. This synthesis is driven by the hydrogenation of CO2 and/or amalgamation of CHx radicals. Global plasma chemistry modeling underscores the pivotal role of electron temperature and CHx radical genesis, contingent upon varying CO2/CH4 ratios in the plasma system. Concomitant with long-chain hydrocarbon production, the system also yields gaseous products, primarily syngas (H2 and CO), as well as liquid-phase alcohols and acids. Our finding demonstrates the feasibility of atmospheric room-temperature synthesis of long-chain hydrocarbons, with the potential for tuning the chain length based on the feed gas composition.

Synthesis and Characterization of a Temperature-Sensitive Microcapsule Gelling Agent for High-Temperature Acid Release.

Deep, high-temperature carbonate reservoirs, represented by the Chuanzhong-Gaomo Block and the Penglai Gas Field, have become important supports for increased storage and production in Sichuan Basin. However, acidization in high-temperature to ultrahigh-temperature reservoirs faces several technical challenges, such as fast acid-rock reaction rates, limited acid corrosion distances, and high risks of tubular corrosion. In this study, a novel high-temperature-resistant microencapsulated gelling agent GLE-3 was prepared using N-isopropylacrylamide (NIPAM) as the wall material, acrylamide (AM), 2-acrylamido-2-methylpropanesulfonic acid (AMPS), and N-vinylcaprolactam (NVCL) as the core materials, and N,N'-methylenebis(acrylamide) (MBA) as the cross-linking agent through inverse emulsion polymerization. GLE-3 was structurally characterized using infrared spectroscopy, transmission electron microscopy, and particle size analysis, and its properties were evaluated. The results showed that GLE-3 exhibited uniform particle size distribution ranging from 10 to 100 μm. Under high-temperature conditions of 180 °C and a shear rate of 170 s-1, the viscosity of the gel acid solution remained above 27.8 mPa·s, with a viscosity retention rate of 63.76%. Compared to GLE-1 (uncapsulated), GLE-3 demonstrated improved thermal stability and shear stability after microencapsulation. After 60 min of shearing at 180 °C and shear rate of 170 s-1, the viscosity retention rate was 88.99%. Furthermore, under 180 °C conditions, GLE-3 exhibited good high-temperature slow-release performance compared to GLE-1, which unencapsulated with the same raw materials. By increasing the viscosity of the gel acid, delaying the acid-rock reaction rate, and providing high-temperature slow-release effects, the high-temperature resistance of the acid system was enhanced, ultimately achieving deep acidization in high-temperature reservoirs.

Cotton stalk decomposition with DBD low-temperature plasma: Characteristics and kinetics

DBD low-temperature plasma (DLTP) is recognized as one of the most efficient technologies for treating cotton stalks. This study investigates the impact of various conditions on the gas production characteristics of cotton stalks (CS) and delves into the DLTP decomposition kinetics of CS and CSC in oxygen-enriched (30 % O2/Ar) and CO2 atmospheres. The decomposition rates of CS followed the order CO2 > N2 > Ar. The decomposition behavior of CSC in oxygen-enriched DLTP (30 % O2/Ar) aligned well with the chemical reaction model. The activation energies for CSC decomposition at 900 °C and 1000 °C were determined to be 23.8 kJ/mol and 33.8 kJ/mol, respectively. Moreover, the reaction rate decreased at higher carbonization temperatures, which proved to be detrimental to the decomposition of CSC. The DLTP decomposition of CSC in CO2 exhibited consistency with the fitting results of the unreacted shrinking core model, revealing an observed activation energy of 19.4 kJ/mol.

Preparation and electrochemical performance of cellulose-based biomass-derived carbon materials

Biomass-derived carbon materials are regarded as an ideal precursor for activated carbon owing to their unique structure, widely used in energy storage applications. Porous biomass carbon materials were prepared by high-temperature carbonization and activation methods using corn stalk stem pith as the carbon source. The structures and morphology of biomass-derived carbon materials were also characterized and analyzed, and it was employed as the electrode material to study the electrochemical properties. The results showed that the specific surface area and pore volume increased with the increase of temperature under the action of the same activator. The activation degree of carbon materials by different activators showed obvious differences under the same temperature conditions, and the structure and properties of the carbon materials obtained by sodium hydroxide activation were better than those obtained by sodium bicarbonate activation. When the temperature was fixed at 900 ℃, the carbon materials obtained by sodium hydroxide activation showed the best structural characteristics and electrochemical properties, with the specific surface area up to 532.881 m2·g−1 and the microporous volume accounting for 76.266 % of the total pore volume. By cyclic voltammetry test, the specific capacity was 139 F·g−1 at a scan rate of 10 mV·s−1, and the electrochemical impedance was much smaller than the impedance of the product obtained by sodium bicarbonate activation. Meanwhile, the specific capacity remained basically unchanged after 1000 cycles of charging and discharging, with excellent cycling stability and electrochemical performance. The relevant results provide a new way for the efficient utilization and functionalization of biomass resources.