High-temperature Pyrolysis Research Articles

Co-crosslinking and anchoring strategy: One-step preparation of N-doped porous carbon for supercapacitors and zinc ion hybrid capacitors

Porous carbon has been widely used in aqueous capacitors due to its wide source, high stability, and controllable preparation. However, the two-step preparation strategy of carbonization and activation with complex operation and serious energy consumption severely limits its further application. In this paper, resorcinol/urea-furfural resin was successfully prepared by using cleaner and greener furfural as raw material and co-crosslinking with resorcinol and urea under the action of catalyst. It is noteworthy that during the curing process, KOH is uniformly anchored inside the resin, so the system only needs one-step high-temperature pyrolysis to obtain a N-doped ant-nest-like three-dimensional interconnected porous carbon material. Consequently, the porous carbon exhibited an impressive specific capacitance of 283F g−1. The assembled symmetrical device shows a capacitance retention of 92 % after 50 000 cycles, showing excellent cycle stability. In addition, the assembled zinc ion hybrid capacitor exhibits a capacitance of 138 mAh g−1 and an energy density of 111 Wh kg−1. The one-step carbonization-doping-activation strategy of this bottom-up in-situ anchoring activator will provide further insights into the hierarchical pore structure design of porous carbon and facilitate the simple and efficient preparation of carbon materials.

Defect-rich hard carbon designed by heteroatom escape assists sodium storage performance for sodium-ion batteries

Sodium-ion batteries (SIBs) avoids the use of expensive cobalt element, and the abundance of sodium element is high, so it shows great application potential, and the development of sodium-ion battery materials is of great value. Biomass precursors have the advantages of low cost and widely and sufficiently distributed resources, and embody the environmental concept of waste utilization, however, the poor reversible specific capacity and initial coulombic efficiency (ICE) of pristine corn stover-derived hard carbons (CSHCs) limit their practical application value. In this paper, we propose a method to increase the reversible specific capacity of hard carbon and maintain high ICE, introduce heteroatoms into graphene-like nanosheets at low carbonization temperature, then escape heteroatoms through high pyrolysis temperature, create defects in the graphene-like carbon layer and expand the (002) layer spacing. Density functional theory (DFT) calculations show that defects are beneficial to the adsorption of Na+ on graphene-like nanosheets, and Na+ have a lower diffusion barrier between layers rich in defects and extended (002) layer spacing. Compared with the conventional low pyrolysis temperature heteroatom doping process, the present method exhibits superior ICE. In the ester-based electrolyte, the modified hard carbon (D-CSHC) exhibits a superior specific capacity of 284.5 mAh/g and an ICE of 85.9 % as compared to the pristine corn stover-derived hard carbon (233.5 mAh/g, 72.7 %). In addition, the capacity retention rate was 92.6 % after 500 turns of constant current cycles at 0.15 A/g.

The Influence of Pyrolysis Temperature and Feedstocks on the Characteristics of Biochar-Derived Dissolved Organic Matter: A Systematic Assessment

Biochar is a carbon-rich product obtained by pyrolyzing biomass under oxygen-limited conditions and has a wide range of potential for environmental applications. In particular, dissolved organic matter (DOM) released from biochar has an important impact on the fate of pollutants. The study aimed to systematically assess how varying pyrolysis temperatures and biomass feedstocks influence the characteristics of biochar-derived DOM. DOM samples were comprehensively characterized utilizing UV-vis spectroscopy and excitation–emission matrix (EEM) fluorescence spectroscopy, coupled with parallel factor (PARAFAC) analysis. The study discovered that pyrolysis temperature significantly affects DOM characteristics more than feedstock type. An increase in pyrolysis temperature correlated with a notable decrease in dissolved organic carbon content, aromaticity, and fluorescence intensity, alongside a marked increase in pH and hydrophilicity. PARAFAC analysis identified three distinct DOM components: two humic-like substances (C1 and C2) and one protein-like substance (C3). The proportion of protein-like substances increased with higher pyrolysis temperatures, while the humic-like substances’ proportion declined. The compositional shifts in DOM with pyrolysis temperature may significantly influence its environmental behavior and functionality. Further research is necessary to explore the long-term environmental impact and potential applications of biochar-derived DOM.

Unveiling dioxin dynamics: A whole-process simulation study of municipal solid waste incineration

Theoretical research has explained the process of dioxin (DXN) formation in the municipal solid waste incineration (MSWI). This process includes the generation, adsorption, and emission of DXN. Actual DXN concentrations often significantly deviate from theoretical models. This discrepancy is influenced by several key factors: the type of integrated municipal solid waste (MSW) treatment process, the characteristics of the waste, and the operational controls. The progression of DXN generation, adsorption, and emission concentrations within the MSWI process remains unclear. This lack of clarity is especially pronounced when examining the accounting for the specific components of the MSW. To unravel the evolution of DXN, this article proposes a comprehensive numerical simulation model for the entire process of DXN concentration in an MSWI plant. The model is designed based on existing knowledge of MSW combustion and DXN mechanisms, leveraging FLIC and ASPEN simulation software. It incorporates six key stages to facilitate the DXN simulation: precipitation and formation, high-temperature pyrolysis, high-temperature gas-phase synthesis, low-temperature catalytic synthesis, adsorption on activated carbon, and emission to the atmosphere. Under both benchmark and multiple operating conditions, the simulated experiments confirm the effective representation of the evolution of DXN concentrations throughout the process. Consequently, this study presents a model designed to enhance the development of strategies aimed at reducing DXN emissions and to foster innovation in intelligent control technologies.

Acceptorless Dehydrogenation under Neat Reaction Conditions: Synthesis of 2-Aryl/Alkyl Quinazolinones Using Supported Ni NPs as Catalyst

AbstractWe report here a Ni-NPs-catalyzed one-pot synthesis of 2-alkyl/aryl quinazolinone motifs via acceptorless dehydrogenation of alcohol, condensation of an aldehyde intermediate with 2-aminobenzamide, followed by a second dehydrogenation of the cyclized intermediate. The protocol is atom-economical and require earth-abundant Ni as the catalyst. The present report involves the annulation of 2-aminobenzamide with various types of primary alcohols, including aryl/heteroaryl methanol, and aliphatic alcohols, and produces high yields of the desired products under neat conditions. The catalyst was synthesized via a high-temperature pyrolysis strategy, using ZIF-8 as the sacrificial template. The Ni NPs@N-C catalyst was characterized by XPS, HR-TEM, HAADF-STEM, XRD, and ICP-MS. The catalyst is stable even in air at room temperature and displayed excellent activity in the acceptorless dehydrogenative coupling synthesis of quinazolinones and could be recycled five times without appreciable loss of its activity.

Design and processing of SiOC/SiC/Si3N4/C ceramics with hierarchical porosity and non-oxide nanostructures

An integral study on the development and characterization of porous SiOC/SiC/Si3N4/C-based ceramic bodies was conducted using a less-explored approach, which is based on the direct consolidation of previously unstudied composite systems (methacryloxypropyl silsesquioxane/sucrose/prepyrolyzed powder), burn-out, and N2 pyrolysis (1300–1400 °C). Their textural, physicochemical, and microstructural properties depended on the initial system composition and pyrolysis temperature; the latter was also decisive in the materials' oxidative stability. At the highest pyrolysis temperature, SiC, mainly in the form of whiskers, and Si3N4 formed, the amount of SiOC decreased, Si2N2O crystallized, and nanocrystalline graphite-type carbon underwent graphitization. The final bodies exhibited macro- and mesopores, with micropores present only in those pyrolyzed at 1300 °C. This latter material presented the highest specific surface area, making it a potential candidate for catalysis in non-oxidizing environments at high temperatures or in oxidizing conditions at lower temperatures. Meanwhile, the material developed at 1400 °C offered high-temperature oxidative stability.

Metal–organic framework derived RuNiMo/NC for enhanced hydrogen production and methanol reforming electrolysis

It is important to probe the effect of doping of ultratrace content of precious metal and synergistic effects of multimetals on effective electrocatalysts for water splitting. Thus, ultratrace content Ru doping NiMo-NC were acquired through simple hydrothermal technology and high-temperature pyrolysis. Benefiting from porous structure, ultratrace content Ru doping and synergistic effect of multiple metals, RuNiMo-NC-2 presents the small overpotentials of 130 and 199 mV for MOR to achieve 10 and 100mA cm−2 in 1 mol/L potassium hydroxide with 5 mol/L methanol. The assembled water electrolyzer with the RuNiMo-NC-2||RuNiMo-NC-2 couple only requires 1.49 V to realize 10mA cm−2 for the overall water splitting in 1 mol/L potassium hydroxide with 5 M methanol. This paper offers a feasible method for designing bifunctional electrocatalysts with superior electrocatalytic performance, which can be used in hydrogen production through water electrolysis.

Heteroatom Immobilization Engineering toward High-Performance Metal Anodes.

Heteroatom immobilization engineering (HAIE) is becoming a forefront approach in materials science and engineering, focusing on the precise control and manipulation of atomic-level interactions within heterogeneous systems. HAIE has emerged as an efficient strategy to fabricate single-atom sites for enhancing the performance of metal-based batteries. Despite the significant progress achieved through HAIE in metal anodes for metal-based batteries, several critical challenges such as metal dendrites, side reactions, and sluggish reaction kinetics are still present. In this review, we delve into the fundamental principles underlying heteroatom immobilization engineering in metal anodes, aiming to elucidate its role in enhancing the electrochemical performance in batteries. We systematically investigate how HAIE facilitates uniform nucleation of metal in anodes, how HAIE inhibits side reactions at the metal anode-electrolyte interface, and the role of HAIE in promoting the desolvation of metal ions and accelerating reaction kinetics within metal-based batteries. Finally, we discuss various strategies for implementing HAIE in electrode materials, such as high-temperature pyrolysis, vacancy reduction, and molten-salt etching and anchoring. These strategies include selecting appropriate heteroatoms, optimizing immobilization methods, and constructing material architectures. They can be utilized to further refine the performance to enhance the capabilities of HAIE and facilitate its widespread application in next-generation metal-based battery technologies.

The Mechanism of Arsenic Release in Contaminated Paddy Soil with Added Biochar: The Role of Dissolved Organic Matter, Fe, and Bacteria.

The addition of biochar inevitably modifies the acidity (pH), redox potential (Eh), and dissolved organic matter (DOM) level in the soil. These alterations also have coupled effects on the cycling of iron (Fe) and the composition of bacterial communities, thereby impacting the speciation and availability of arsenic (As) in the soil. This study explored the potential mechanisms through which biochar affects As in paddy soil during flooded cultivation with different pyrolysis temperature biochars (300 °C, 400 °C, and 500 °C) added. The results revealed that the TAs concentration increased in the initial 15 days of soil cultivation with SBC300 or SBC400 addition because increasing the concentration of DOM induced the mobility of As though the formation of As-DOM complexes. Meanwhile, biochar addition elevated the pH, decreased the Eh, and promoted the transformation of specific adsorbed As (A-As) and amorphous iron oxide-bound As (Amo-Fe-As) to supernatant As through enhancing the reductive dissolution of Fe(oxy)(hydr)oxides. Moreover, the biochar altered the relative abundance of As (V)-reducing bacteria (such as Firmicutes) and As (III)-oxidizing bacteria (such as Chloroflex), thereby affecting As speciation. However, these mechanistic effects varied depending on the pyrolysis temperature of the biochar. The microbial composition of SBC300 and SBC400 were similar, with both containing larger populations of Enterobacteriaceae (AsRB) and pseudomonas (FeRB) compared to CK and SBC500. It was proposed that lower pyrolysis temperatures (300 °C and 400 °C) are more favorable for the dissolution of Fe(oxy)(hydr)oxides and the reduction of As (V). However, the biochar from the higher pyrolysis temperature (500 °C) showed environmental impacts akin to the control group (CK). This study demonstrated potential mechanisms of biochar's effect on As and the role of pyrolysis temperature.

Inflammation-free electrochemical in vivo sensing of dopamine with atomic-level engineered antioxidative single-atom catalyst

Electrochemical methods with tissue-implantable microelectrodes provide an excellent platform for real-time monitoring the neurochemical dynamics in vivo due to their superior spatiotemporal resolution and high selectivity and sensitivity. Nevertheless, electrode implantation inevitably damages the brain tissue, upregulates reactive oxygen species level, and triggers neuroinflammatory response, resulting in unreliable quantification of neurochemical events. Herein, we report a multifunctional sensing platform for inflammation-free in vivo analysis with atomic-level engineered Fe single-atom catalyst that functions as both single-atom nanozyme with antioxidative activity and electrode material for dopamine oxidation. Through high-temperature pyrolysis and catalytic performance screening, we fabricate a series of Fe single-atom nanozymes with different coordination configurations and find that the Fe single-atom nanozyme with FeN4 exhibits the highest activity toward mimicking catalase and superoxide dismutase as well as eliminating hydroxyl radical, while also featuring high electrode reactivity toward dopamine oxidation. These dual functions endow the single-atom nanozyme-based sensor with anti-inflammatory capabilities, enabling accurate dopamine sensing in living male rat brain. This study provides an avenue for designing inflammation-free electrochemical sensing platforms with atomic-precision engineered single-atom catalysts.

Reassessment of the High-Temperature Oxidation of Di Ethyl Ether through Ab Initio Calculations.

Recent investigations of diethyl ether (DEE) high-temperature pyrolysis and fuel-rich oxidation have highlighted the failure of existing kinetic models to describe experimental CO production. The DEE high-temperature pyrolysis and oxidation chemistry is thus investigated through ab initio calculations. Geometries, frequencies, and hindered-rotor potentials of reactants, products, and transition states of key reactions (fuel decomposition radical decomposition and H-abstraction reactions) are calculated with the B2PLYP-D3/def2-TZVPD method, whereas final energies are refined using CCSD(T)/aug-cc-pV(D,T)Z. Temperature- and pressure-dependent rate constants are then derived from either canonical transition state theory (CTST) or ME/RRKM analysis with the inclusion of tunneling effect and hindered-rotor corrections and compared to experimental measurements when available as well as to previously suggested values. This new information is then merged with a C0-C3 core chemistry model and a low-temperature chemistry DEE subset from the literature to propose a new kinetic model for the combustion of DEE. This model is tested successfully against a large database related to the high-temperature oxidation and pyrolysis chemistry of DEE, including ignition delay times, shock tube speciation data, time-resolved CO profiles, laminar flame speeds, flame structures, and jet-stirred reactor data.

CuO-Fe3C-C modified PVDF membrane for catalysis and antifouling

Modification of membranes is an effective method for degrading organic pollutants and alleviating membrane fouling. In this study, CuO-Fe3C-C catalyst was prepared by high-temperature pyrolysis. The membrane modified by CuO- Fe3C-C was prepared by vacuum filtration. The bacteriostatic rate of the modified membrane can reach to 96.8 %. Compared to the pristine membrane, the pure water flux of the modified membrane increased from 223.43 L m−2h−1 bar−1 to 422.27 L m−2h−1 bar−1, the flux recovery ratio (FRR) of modified membranes increased from 39.7 % to 79.25 %. Removal rate of TC (Tetracycline) by modified membrane activated PMS can reach to 90.75 %. After 5 cycles, the degradation efficiency of modified membranes was still 83.77 %, which was only 6.39 % lower than that of the first cycle. Free radical quenching experiments and ESR tests explored the possible catalysis and antifouling mechanisms of the modified membrane system, the results showed main active species were SO4−•, OH•, O2−• and 1O2. This study prepared membranes with excellent antifouling properties, providing a theoretical reference for alleviating membrane fouling in membrane-based water treatment.

Characterization and photocatalytic properties of zno tetrapods synthesized by high-temperature pyrolysis

The presented work presents the structural and morphological characterization and the results of studies of luminescent, photocatalytic properties of ZnO tetrapods synthesized by the method of high-temperature pyrolysis. It has been shown that the morphology and structural parameters of ZnO tetrapods are determined by the location in the synthesis zone (correlated with the distance from the air inflow window). All samples were characterized by pseudo-three-dimensional morphology of tetrapods. A correlation was found between luminescent properties and photocatalytic activity of tetrapods. The highest photodegradation rates of methylene blue under ultraviolet radiation were demonstrated by ZnO tetrapods grown in the zones closest and farthest from the window (rate constants 54 × 10–3 min–1 and 50 × 10–3 min–1, respectively).

BN fiber aerogels with high solar reflectivity and thermal insulation for green buildings

There exists more than one-third of the stock of buildings that do not meet energy-saving building standards, so there is an urgent need for breakthroughs in the field of green buildings. Herein, we successfully prepared boron nitride (BN) fiber aerogels by sol-gel, freeze-drying and high-temperature pyrolysis. When the molar ratio of C3N6H6 to H3BO3 was 1:2 and the roasting temperature was 1000 °C, the BN fiber aerogel was produced with high specific surface area (257.690 m2/g) and high porosity (99 %). BN fiber aerogels, with their low thermal conductivity (0.043 W/(m·K)) and stable mechanical properties (no change after 45 cycles at 30 % strain), offered possibilities for thermal insulation in green buildings. Its hydrophobic properties protect the wall from the natural environment. In particular, it had a solar reflectivity of 98.6 %, which exceeds most reflective coating materials, enabling the cooling of green construction on hot summer days. The high-temperature resistance of BN fiber aerogels could be applied in special environments such as blast furnace plants and thermoelectric power plants.

Chemiluminescence during the high-temperature pyrolysis and oxidation of ammonia

Chemiluminescent emissions from NH2*, NH*, NO*, and OH* during the pyrolysis and oxidation of ammonia (NH3) are quantitatively characterized to gain insight into their reaction mechanisms. Time profiles of light emitted from high-temperature reactions of NH3/Ar and NH3/O2/Ar mixtures have been measured behind reflected shock waves at temperatures of 2300–2600 K and pressures of 1.6–1.9 bar in a high-repetition-rate shock tube. The emission intensities have been calibrated based on the well-characterized OH* chemiluminescence in a hydrogen-oxygen system and converted to photon emission rates for quantitative comparison with kinetic simulations. A kinetic model describing the pyrolysis and oxidation of ammonia and reactions of excited species has been constructed by combining the reaction mechanisms proposed in recent modeling studies. With only modest updates of the thermodynamic functions and the rate constants for the formation and quenching of excited species, the observed chemiluminescence profiles could be reasonably reproduced, with a few exceptions. The rate of production analysis indicates that NH2* is produced by the reaction of NH3 with H as well as thermal excitation of NH2, that the energy transfer reactions from 3N2 to NH and NO are responsible for the formation of NH* and NO*, respectively, and that the formation of OH* is competitively contributed by the reactions of H with N2O, 3N2 with OH, and NH with NO. Remaining discrepancies between the experiment and modeling are noted, and potential directions for further model improvement are discussed.

Solid-state Ru(bpy)32+ electrochemiluminescence sensor for trace detection of fenpropathrin using loofah sponge-like carbon nanofibers and CdS.

Loofah sponge-like carbon nanofibers (LF-Co,N/CNFs) were utilized as a carrier for Ru(bpy)32+, and then combined with CdS to create a novel solid-state electrochemiluminescence sensor capable of detecting trace amounts of fenpropathrin. LF-Co,N/CNFs, obtained through the high-temperature pyrolysis of ZIF-67 coaxial electrospinning fibers, were characterized by a loofah-like morphology and exhibited a significant specific surface area and porosity. Apart from serving as a carrier, LF-Co,N/CNFs also functioned as a luminescence accelerator, enhancing the system's luminescence efficiency by facilitating electron transmission and reducing the transmission distance. The inclusion of CdS in the luminescence reaction, in conjunction with Ru(bpy)32+, further boosted the sensor's luminescence signal. The resulting sensor demonstrated a satisfactory signal, with fenpropathrin causing significant quenching of the ECL signal.Under optimized conditions, a linear relationship between the signal quench value and fenpropathrin concentration in the range 1 × 10-12 to 1 × 10-6M was observed, with a detection limit of 3.3 × 10-13M (S/N = 3). This developed sensor ischaracterized by its simplicity, sensitivity, and successful application in detecting fenpropathrin in real samples. The study not only presentsa straightforward detection platform for fenpropathrin but also introduces new avenues for the rapid determinationof various food contaminants, thereby expanding the utility of carbon fibers in electrochemiluminescence sensors.

Dispersion of ZnO or TiO2 nanoparticles onto P. australis stem-derived biochar for highly efficient photocatalytic removal of doxycycline antibiotic under visible light irradiation

Abstract Biochar (BC) derived from reed stems was prepared by high-temperature pyrolysis, and two types of ZnO/biochar (ZBC) and TiO2/biochar (TBC) composite materials were synthesized via a simple hydrolysis method. These composites, compared to pure ZnO and TiO2, exhibit not only improved but significantly enhanced crystalline structures and larger specific surface areas. This enhancement in the physical and chemical properties of ZBC and TBC composites is a crucial aspect of our research, as it leads to a distinct red-shifted absorption edge and excellent visible-light absorption characteristics. The photocatalytic degradation efficiency of ZBC and TBC composite materials, a key finding of our study, was evaluated using doxycycline antibiotic as a simulated pollutant under visible-light irradiation. The results demonstrate a 6.0-fold and 7.3-fold increase in photocatalytic degradation efficiency of ZBC and TBC composites compared to pure ZnO and TiO2, respectively, further underscoring the significance of these enhanced properties. Furthermore, active species trapping experiments reveal that ·OH radicals are the dominant reactive species in the photocatalytic degradation process of doxycycline. A Langmuir–Hinshelwood kinetic model accurately represents this degradation process. Kinetic data indicate that the degradation rate constants (k) of ZBC and TBC catalysts are 4.314 × 10−2 min−1 and 3.416 × 10−2 min−1, respectively. The photocatalysts exhibit no significant decrease in degradation efficiency for ZBC and TBC even after the fourth cycle, indicating their relatively high reusability. These results suggest that ZBC and TBC materials can be used as stable, efficient, cost-effective, and sustainable photocatalytic composite materials for antibiotic-contaminated wastewater treatment.

Insight into high-temperature fast pyrolysis characterization, product distribution and interaction effect of municipal solid waste and its components under steam-containing hydrogen-rich syngas atmosphere

This research delves into the field of fast hydropyrolysis of mixed municipal solid waste (MSW), with the goal of understanding product distribution and interactions in a hydrogen-rich condition. Through experimental investigations on MSW and its components, this study thoroughly examines the impact of pyrolysis temperature and gasification atmosphere (30 % H2+30 % CO+20 % CO2+20 % H2O) on the yields and distribution of the three-phase products. As the temperature increases, the gas yield gradually increases, while the yields of tar and char gradually decrease. The introduction of a hydrogen source increases the methane content in the combustible gas, which generally reaches its maximum at 850 °C, and promotes aromatic formation in tar, making aromatics the main component of pyrolysis oil. Notably, aromatics have the highest-octane number in gasoline. This study highlights gasification as a promising technology for converting organic waste into valuable fuel, advancing waste management and energy recovery.

The cation exchange driving multi-phase regulation in Co7Fe3/Co@NC for enhanced broadband electromagnetic wave absorption

Phase engineering offers distinctive advantages in designing efficient electromagnetic wave (EMW) absorbers. The manipulation of the interaction and arrangement of different multi-phase systems enables the achievement of more precise EMW absorption. However, the transition mechanism from single metal phases to metal/alloy phases has not yet been fully revealed. Here, we employ multiphase engineering driven by cation exchange reactions to finely control the proportion of Co/Co7Fe3 phases and regulate electromagnetic parameters. The introduction of cavities and heteroatoms through cation exchange enables optimized defect distribution and composition, which enhances both impedance matching and electromagnetic attenuation capabilities. Specifically, we yield hollow Co7Fe3/Co@N-doped carbon (H-Co7Fe3/Co@NC) embedded in high-crystallinity graphite carbon after high-temperature pyrolysis, which promotes significant electron transfer between phases, thus enhancing conduction and polarization losses. H-Co7Fe3/Co@NC exhibits ultra-strong reflection loss (RL) of −59.70 dB at 9.37 GHz and achieves broadband absorption of 6.01 GHz at 2.1 mm. This study highlights the influence of Co7Fe3/Co heterogeneous structures on absorption performance and validates the electromagnetic response mechanism of multi-phase heterostructures through COMSOL finite element simulation analysis. Thus, this work paves the way for applying multi-phase engineering driven by cation exchange reactions for advanced absorbers.

Pre-combustion mercury removal potential of rapid pyrolysis in high ash coal and mode of occurrence

Mercury is a widely known pollutant, and coal combustion is one of the largest sources of anthropogenic Hg emission. Mercury reduction technologies globally rely on flue gas treatment. However, pre-combustion techniques show immense potential. Mild pyrolysis of coal offers a promising approach for mitigating mercury emissions. This study investigated the mercury distribution and its mode of occurrence in six high ash coal samples from the Jagannath area of eastern India. The findings revealed that Hg content in coal samples ranged from 0.154-0.308 mg/kg. Majority of the mercury was bound to pyrites (60–90 %) and organic matter (5–15 %). Rapid pyrolysis at temperatures ranging from 200 to 700 °C demonstrated significant mercury removal efficiency (up to 95 %). In particular, at 400 °C with minimal loss in calorific value and mass. Though the high-temperature pyrolysis (600 °C) resulted in maximum mercury removal, but with a notable loss in calorific value and product yield. The Hg content in raw coal, initially ranging from 9 to 20 μg Hg/MJ, was reduced to 3 to 11 μg Hg/MJ in char produced at 400 °C. Further reduction was observed in char produced at 600 °C, where the Hg content decreased to between 2–3 μg Hg/MJ. This research emphasizes the effectiveness of mild pyrolysis in reducing mercury content of high ash coal, thereby facilitating the generation of cleaner energy.