Ultra-efficient removal of aqueous hexavalent chromium by activated biochar nanoparticles derived from squid ink.

Biochar have been recognized as efficient and renewable carbon sorbents, which attracted much attention on Cr contamination remediation in wastewater. In this study, we propose a cost-effective one-step strategy to synthesize activated biochar nanoparticles derived from squid ink (AS-BC) for aqueous Cr(VI) removal. The results demonstrated that AS-BC achieved a removal rate of 24.29 h-1 at 700 °C (400-times higher than the unmodified one). This was also a state-of-the-art removal performance for aqueous Cr(VI) compared to other reported materials. AS-BC possessed an enormous specific surface (2408 m2/g at 700 °C) with abundant O- and N-containing groups, condensed aromatic structures, and high electron transfer capacity (3.64 and 2.13 mmol e-/g for EAC and EDC at 700 °C), contributing to the ultra-efficient removal of Cr(VI) by synergistic adsorption and reduction. AS-BC absorbed Cr(VI) in the form of HCrO4- by electrostatic attraction with protonated amine-N and hydroxy (-NH3+ and -OH2+) groups and Cr(III) in the form of Cr3+ by complexation with amine-N and hydroxy groups. With a hydroxy-quinone and conjugated π-electron system, AS-BC served as mediator and shuttle to accelerate electron transfer in Cr(VI) reduction with an electron donor. Therefore, our findings highlight the immense potential of AS-BC biochar nanoparticles represent a potential alternative for high-performance Cr(VI) remediation in wastewater.

Preparation of Oily Sludge-Derived Activated Carbon and Its Adsorption Performance for Tetracycline Hydrochloride.

Oily sludge-derived activated carbon was prepared using the potassium hydroxide (KOH) activation method using oily sludge as a raw material, and one-factor experiments determined the best conditions for preparing activated carbon. The activated carbon's morphological structure and surface chemical properties were analyzed by scanning different characterization tools, and the adsorption behavior of tetracycline hydrochloride was investigated. The results showed that the optimum conditions for preparing oily sludge-derived activated carbon were an activation temperature of 400 °C, activation time of 30 min, activator concentration of 1 mol/L, and impregnation ratio of 2 mL/g. After activation, the activated carbon had more pores and a more orderly crystal structure arrangement, the specific surface area was 2.07 times higher than that before activation, and the surface was rich in functional groups such as -HO, -C-O, -C=C, and -C-H, which increased the active sites of activated carbon. Physicochemical effects dominated the adsorption process. It belonged to the spontaneous heat absorption process under the quasi-secondary kinetic and Langmuir isothermal models. The maximum monolayer adsorption capacity of KOH-activated carbon was 205.1 mg·g-1.

One-Pot Synthesis of Melamine Formaldehyde Resin-Derived N-Doped Porous Carbon for CO2 Capture Application.

The design and synthesis of porous carbons for CO2 adsorption have attracted tremendous interest owing to the ever-soaring concerns regarding climate change and global warming. Herein, for the first time, nitrogen-rich porous carbon was prepared with chemical activation (KOH) of commercial melamine formaldehyde resin (MF) in a single step. It has been shown that the porosity parameters of the as-prepared carbons were successfully tuned by controlling the activating temperature and adjusting the amount of KOH. Thus, as-prepared N-rich porous carbon shows a large surface area of 1658 m2/g and a high N content of 16.07 wt%. Benefiting from the unique physical and textural features, the optimal sample depicted a CO2 uptake of up to 4.95 and 3.30 mmol/g at 0 and 25 °C under 1 bar of pressure. More importantly, as-prepared adsorbents show great CO2 selectivity over N2 and outstanding recyclability, which was prominently important for CO2 capture from the flue gases in practical application. An in-depth analysis illustrated that the synergetic effect of textural properties and surface nitrogen decoration mainly determined the CO2 capture performance. However, the textural properties of carbons play a more important role than surface functionalities in deciding CO2 uptake. In view of cost-effective synthesis, outstanding textural activity, and the high adsorption capacity together with good selectivity, this advanced approach becomes valid and convenient in fabricating a unique highly efficient N-rich carbon adsorbent for CO2 uptake and separation from flue gases.

Nitrogen-doped porous carbons from polyacrylonitrile fiber as effective CO2 adsorbents.

In this report, nitrogen-doped porous carbons were synthesized from polyacrylonitrile fiber by a facile two-step synthesis process i.e. carbonization followed by KOH activation. Activation temperature and KOH/carbon ratio are two parameters to tune the porosity and surface chemical properties of sorbents. The as-obtained sorbents were carefully characterized. Special attention was paid concerning the change of sorbents' morphology with respect to synthesis conditions. Under the activation temperatures of this study, the sorbents can still retain their fibrous structure when the KOH/carbon mass ratio is 1. Further increasing the KOH amount will destroy the original morphology of polyacrylonitrile fiber. CO2 adsorption performance tests show that a sorbent retaining the fibrous shape possesses the highest CO2 uptake of 3.95 mmol/g at 25°C and 1 bar. Comprehensive investigation found that the mutual effect of narrow microporosity and doped N content govern the CO2 adsorption capacity of these adsorbents. Furthermore, these polyacrylonitrile fiber-derived carbons present multiple outstanding CO2 capture properties such as excellent recyclability, high CO2/N2 selectivity, fast adsorption kinetics, suitable heat of adsorption, and good dynamic adsorption capacity. Hence, nitrogen-doped porous carbons with fibrous structure are promising in CO2 capture.

KOH activated nitrogen and oxygen co-doped tubular carbon clusters as anode material for boosted potassium-ion storage capability.

Carbon nanomaterials have become a promising anode material for potassium-ion batteries (KIBs) due to their abundant resources, low cost, and excellent conductivity. However, among carbon materials, the sluggish reaction kinetics and inferior cycle life severely restrict their commercial development as KIBs anodes. It is still a huge challenge to develop carbon materials with various structural advantages and ideal electrochemical properties. Therefore, it is imperative to find a carbon material with heteroatom doping and suitable nanostructure to achieve excellent electrochemical performance. Benefiting from a Na2SO4template-assisted method and KOH activation process, the KOH activated nitrogen and oxygen co-doped tubular carbon (KNOCTC) material with a porous structure exhibits an impressive reversible capacity of 343 mAh g-1at 50 mA g-1and an improved cyclability of 137 mAh g-1at 2 A g-1after 3000 cycles with almost no capacity decay. The kinetic analysis indicates that the storage mechanism in KNOCTC is attributed to the pseudocapacitive process during cycling. Furthermore, the new synthesis route of KNOCTC provides a new opportunity to explore carbon-based potassium storage anode materials with high capacity and cycling performance.

One-Pot Synthesis of N-Rich Porous Carbon for Efficient CO2 Adsorption Performance.

N-enriched porous carbons have played an important part in CO2 adsorption application thanks to their abundant porosity, high stability and tailorable surface properties while still suffering from a non-efficient and high-cost synthesis method. Herein, a series of N-doped porous carbons were prepared by a facile one-pot KOH activating strategy from commercial urea formaldehyde resin (UF). The textural properties and nitrogen content of the N-doped carbons were carefully controlled by the activating temperature and KOH/UF mass ratios. As-prepared N-doped carbons show 3D block-shaped morphology, the BET surface area of up to 980 m2/g together with a pore volume of 0.52 cm3/g and N content of 23.51 wt%. The optimal adsorbent (UFK-600-0.2) presents a high CO2 uptake capacity of 4.03 mmol/g at 0 °C and 1 bar. Moreover, as-prepared N-doped carbon adsorbents show moderate isosteric heat of adsorption (43-53 kJ/mol), acceptable ideal adsorption solution theory (IAST) selectivity of 35 and outstanding recycling performance. It has been pointed out that while the CO2 uptake was mostly dependent on the textural feature, the N content of carbon also plays a critical role to define the CO2 adsorption performance. The present study delivers favorable N-doped carbon for CO2 uptake and provides a promising strategy for the design and synthesis of the carbon adsorbents.

Efficient nitrogen doped porous carbonaceous CO2 adsorbents based on lotus leaf.

In this work, the waste biomass lotus leaf was converted into N-doped porous carbonaceous CO2 adsorbents. The synthesis process includes carbonization of lotus leaf, melamine post-treatment and KOH activation. For the resultant sorbents, high nitrogen content can be contained due to the melamine modification and advanced porous structure were formed by KOH etching. These samples were carefully characterized by different techniques and their CO2 adsorption properties were investigated in detail. These sorbents hold good CO2 adsorption abilities, up to 3.87 and 5.89 mmol/g at 25 and 0°C under 1 bar, respectively. By thorough investigation, the combined interplay of N content and narrow microporous volume was found to be responsible for the CO2 uptake for this series of sorbents. Together with the high CO2 adsorption abilities, these carbons also display excellent reversibility, high CO2/N2 selectivity, applicable heat of adsorption, fast CO2 adsorption kinetics and good dynamic CO2 adsorption capacity. This study reveals a universal method of obtaining N-doped porous carbonaceous sorbents from leaves. The low cost of raw materials accompanied by easy synthesis procedure disclose the enormous potential of leaves-based carbons in CO2 capture as well as many other applications.

Superior CO2 uptake on nitrogen doped carbonaceous adsorbents from commercial phenolic resin.

In this study, N-doped porous carbons were produced with commercial phenolic resin as the raw material, urea as the nitrogen source and KOH as the activation agent. Different from conventional carbonization-nitriding-activation three-step method, a facile two-step process was explored to produce N-incorporated porous carbons. The as-obtained adsorbents hold superior CO2 uptake, i.e. 5.01 and 7.47 mmol/g at 25 °C and 0 °C under 1 bar, respectively. The synergistic effects of N species on the surface and narrow micropores of the adsorbents decide their CO2 uptake under 25 °C and atmospheric pressure. These phenolic resin-derived adsorbents also possess many extremely promising CO2 adsorption features like good recyclability, quick adsorption kinetics, modest heat of adsorption, great selectivity of CO2 over N2 and outstanding dynamic adsorption capacity. Cheap precursor, easy preparation strategy and excellent CO2 adsorption properties make these phenolic resin-derived N-doped carbonaceous adsorbents highly promising in CO2 capture.

Synthesis of high-performance hierarchically porous carbons from rice husk for sorption of phenol in the gas phase.

Phenol as a semi-volatile organic compound (SVOC) extensively presents in industrial wastewater. Moreover, it is a main compound of tar existing in the vapor phase from biomass pyrolysis or gasification. So far, most of works on the phenol adsorption by activated carbons have been conducted in the liquid phase. However, the adsorption of phenol in the gas phase has not been reported. This work aims to synthesize the hierarchically porous carbons from the unaltered and pelletized rice husk (RH) via a facile pyrolysis followed by the ball-milling-assisted KOH activation. Herein, the silica nanoparticles in RH acted as a self-template to remarkably increase specific surface areas and pores, thereby giving rise to the formation of hierarchically porous carbons, which showed a relatively high adsorption capacity (maximum value: 1919 mg/g) of phenol in the vapor phase. Generally, the process of phenol adsorption onto porous carbons in the gas phase followed with various interactions, including pore filling, electrostatic interaction, hydrophobic effect, and functional groups effect (e.g., π-π interaction). And the pseudo-second-order model could well describe the adsorption kinetic. It is noted that the pelletized RH was more favorable to develop the porous carbons with the hierarchically meso-microporous structures that could enhance the transfer of the phenol molecules via the outer layer and subsequent uptake by the adsorption sites on the inner layer. Further, the SVOC phenol was hard to volatilize under ambient conditions due to its relatively higher boiling point (181.7 °C), so the thermal desorption was a potential way to regenerate the spent activated biochars.

Porous carbons derived from polyethylene terephthalate (PET) waste for CO2 capture studies.

Oxygen augmented carbon adsorbent has been developed using polyethylene terephthalate (PET) waste by first carbonizing at different temperatures (500-800 °C) and then chemically activating using different ratios of KOH: PET (mass ratio 1 to 4). The textural characterization divulges the effect of activation in terms of the development of the high surface area and micropore volume of 1690 m2 g-1 and 0.78 cm3 g-1 respectively, for the optimum sample (PET-3-700). Elemental analysis of PET-3-700 illustrates the presence of 34.33% oxygen and XPS results confirmed the occurrence of oxygen moieties which enhance the basicity of the adsorbent and promote CO2 capture. The CO2 adsorption capacity of prepared carbons was determined thermogravimetrically under dynamic conditions, at different concentrations of CO2 (6-100%) and temperatures. The maximum CO2 uptake capacity of 2.31 mmol g-1 was exhibited by PET-3-700 at an adsorption temperature of 30 °C under 100% pure CO2 flow. Four adsorption-desorption cycles corroborate almost complete regenerability of the prepared adsorbent. Adsorption kinetics at all adsorption conditions was described best by fractional order kinetic model. Freundlich isotherm fit indicates the surface of adsorbent being heterogeneous and low values of isosteric heat shows physisorption behavior of the process. Negative values of thermodynamic parameters indicate exothermic and feasible nature of adsorption process.

Adsorption of CO2 on KOH activated carbon adsorbents: Effect of different mass ratios.

Nitrogen and oxygen enriched carbons were prepared by the cost-effective synthesis route of carbonization of polyacrylonitrile (PAN) and subsequent KOH activation for CO2 capture. The effect of four impregnation mass ratios (KOH: PAN = 1-4) and activation temperatures (600-900 °C) on the synthesized carbon adsorbent properties was explored by different analyses. The X-ray photoelectron spectroscopy (XPS) revealed the existence of basic nitrogen and oxygen functionalities on the adsorbent's surface which increases the adsorption rate for CO2 by providing its basic sites. By increasing mass ratio (KOH:PAN) from 1:1 to 3:1, the surface area increased from 1152.4 to 1884.2 m2 g-1 and the dynamic CO2 adsorption capacity also increased from 2.1 to 2.5 mmol g-1 respectively, at 30 °C (approximately ten times the adsorption capacity of untreated PAN, 0.22 mmol g-1). Physisorption and exothermic nature of the process were confirmed by the decrease in the adsorption capacity of the adsorbents with the increase in adsorption temperature. Moreover, good cyclic stability and regenerability over 5 adsorption-desorption cycles were obtained for the adsorbents. The fractional order kinetic and Temkin isotherm models fitted best with the adsorption data. A heterogeneous interaction between CO2 and the surface of adsorbents was suggested by the isosteric heat of adsorption values. Combined with the simple method for the preparation of activated carbon adsorbents, efficient CO2 adsorption and excellent regeneration make it appropriate adsorbents for post-combustion CO2 capture.

Preparation of activated petroleum coke for removal of naphthenic acids model compounds: Box-Behnken design optimization of KOH activation process.

This study employed Box-Behnken design and response surface methodology to optimize activation parameters for the production of activated petroleum coke (APC) adsorbent from petroleum coke (PC) to achieve highest adsorption capacity for three model naphthenic acids. Activated petroleum coke (APC) adsorbent with a BET surface area of 1726 m2/g and total pore volume of 0.85 cc/g was produced at the optimum activation conditions (KOH/coke mass ratio) of 3.0, activation temperature 790 °C, and activation time 3.47 h). Effects of the activation parameters on the adsorption pefromances (adsortion capaciy and kinetics) were investigated. With the APC obtained at the optimum activation condition, the maximum adsorption capacity of 451, 362, and 320 (mg/g) was achieved for 2-naphthoic acid, diphenylacetic acid and cyclohexanepentanoic acid (CP), respectively. Although, generally APC adsorbents with a higher specific surface area and pore volume provide better adsorption capacity, the textural properties (surface areas and pore volume) are not the only parameters determining the APC adsorbents' adsorption capacity. Other parameters such as surface functionalities play effective roles on the adsorption capacity of the produced APC adsorbents for NAs. The KOH activation process, in particular the acid washing step, distinctly reduced the sulfur and metals contents in the raw PC, decreasing the leaching potential of metals from APC adsorbents during adsorption.

Creating Pores on Graphene Platelets by Low-Temperature KOH Activation for Enhanced Electrochemical Performance.

KOH activation of microwave exfoliated graphite oxide (MEGO) is investigated in detail at temperatures of 450-550 °C. Out of the activation temperature range conventionally used for the preparation of activated carbons (>600 °C), the reaction between KOH and MEGO platelets at relatively low temperatures allows one to trace the structural transition from quasi-two-dimensional graphene platelets to three-dimensional porous carbon. In addition, it is found that nanometer-sized pores are created in the graphene platelets at the activation temperature of around 450 °C, leading to a carbon that maintains the platelet-like morphology, yet with a specific surface area much higher than MEGO (e.g., increased from 156 to 937 m(2) g(-1) ). Such a porous yet highly conducting carbon shows a largely enhanced electrochemical activity and thus improved electrochemical performance when being used as electrodes in supercapacitors. A specific capacitance of 265 F g(-1) (185 F cm(-3) ) is obtained at a current density of 1 A g(-1) in 6 m KOH electrolyte, which remains 223 F g(-1) (156 F cm(-3) ) at the current density of 10 A g(-1) .

Alkali modified hydrochar of grape pomace as a perspective adsorbent of Pb(2+) from aqueous solution.

Hydrochar produced via hydrothermal carbonization of grape pomace was considered as novel sorbent of Pb(2+) from aqueous solution. In order to enhance the adsorption capacity, hydrochar was chemically modified using 2 M KOH solution. Both materials were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy and X-ray diffraction technique. Batch experiments were performed to examine the effect of sorbent dosage, pH and contact time. Obtained results showed that the KOH treatment increased the sorption capacity of hydrochar from 27.8 mg g(-1) up to 137 mg g(-1) at pH 5. Adsorption of lead on either of the materials was achieved through ion-exchange mechanism, chemisorption and Pb(2+)-π interaction. The Sips isotherm model gave the best fit with the experimental data obtained for Pb(2+) sorption using activated hydrochar. The adsorption kinetic followed a pseudo second-order model. Thermodynamic parameters implied that the Pb(2+) binding for hydrochar surface was spontaneous and exothermic process. Findings from this work suggest that the hydrothermal carbonization is a promising route for production of efficient Pb (2+) sorbents for wastewater treatment.

Mesoporous carbon particles by biomass waste based on sulfonation and copper oxide functionalization as efficient and stable electrode material for supercapacitor.

Here, the hierarchical mesoporous-activated carbon particles obtained by KOH activation from pistachio shell wastes are modified by both the sulfonation process and CuO doping by hydrothermal heating (CuO@S-doped PSAC) for use as a supercapacitor. It is predicted that the electrochemical performance of the porous carbon electrode material obtained by such CuO doping and sulfonation process will be significantly increased with increased Faradaic capacitance. The electrochemical performance of CuO@S doped PSAC composite is systematically investigated by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and galvanostatic charge/discharge (GCD) in the presence of 1 M H2SO4, 1 M Na2SO4, and 1 M NaOH as electrolytes. The CuO@S doped PSAC-based electrode shows excellent stability with high specific capacitance up to 397.16 F/g at 0.1 A/g and 92.64% retention. Furthermore, FTIR, SEM, XRD, EDS, and nitrogen adsorption/desorption analyses are used for the characterisation of the obtained composites. Based on a significant supercapacitor performance, the synthesis strategy of carbon-based electrode material containing sulfonation and CuO modifications derived from agricultural biomass waste material is predicted to be a valuable example.

Iodine intercalation-assisted alkali activation constructs coal-based porous carbon for high-performance supercapacitors.

Supercapacitors have the advantages of fast charging and discharging speeds, high power density, long cycle life, and wide operating temperature range. They are widely used in portable electronic equipment, rail transit, industry, military, aerospace, and other fields. The design and preparation of low-cost, high-performance electrode materials still pose a bottleneck that hinders the development of supercapacitors. In this paper, coal was used as the raw material, and the coal-based porous carbon electrode material was constructed using the iodine intercalation-assisted activation method and used for supercapacitors. The CK-700 electrode exhibits excellent charge storage performance in a 6 M potassium hydroxide (KOH) electrolyte, with a maximum specific capacitance of 350 F/g at a current density of 0.5 A/g. In addition, it has an excellent rate performance (310 F/g at 1 A/g) and cycle stability (capacitance retention up to 91.7 % after 30000 cycles). This work provides a method for realizing high-quality, high-yield and low-cost preparation of coal-based porous carbon, and an idea for improving the performance of supercapacitors.

Highly efficient activation of peroxymonosulfate via KOH-activated Fe@NC for the degradation of bisphenol A.

In this study, the KOH-modified Fe-ZIF-derived carbon materials (Fe@NC-KOH-x) were designed for Fenton-like systems to enhance bisphenol A (BPA) removal from wastewater. Compared with the Fe@NC without KOH activation, the pore structure, BET (Brunner-Emmet-Teller) surface area, and oxygen-containing functional group of KOH-activated Fe@NC-KOH-x are dramatically improved, which increases the adsorption and catalytic performance. The Fe@NC-KOH-900/PMS system showed significant BPA removal reactivity across wide pH ranges and low doses of Fe@NC-KOH-900. Interestingly, our findings indicated that the removal effectiveness of BPA improved when PMS was introduced following the saturation adsorption of Fe@NC-KOH-x, as compared to the simultaneous introduction of Fe@NC-KOH-x and PMS. More particularly, through regression analysis, we found that the proportion of reactive species in the Fe@NC-KOH-x/PMS system changes with the increase of pyrolysis temperature, and there was a certain relationship between structure-function and active species in the Fe@NC-KOH-x/PMS system. O-C = O, Fe-N4, C-O, and pyrrolic N in Fe@NC-KOH-x lead to the generation of •OH, and SO4-•, C = O, Fe-N4, and defect are closely related to FeIV = O, and the formation of 1O2 is affected by Fe-N4, graphite N, C = O, and defect. Also, the density functional theory (DFT) calculation and the potential correlation between catalyst active centers and reactive oxygen species indicate that Fe-N4 is the main active site of Fe@NC-KOH-x. These outcomes of the study offer an innovation for enhanced elimination of BPA in wastewater treatment and provide a dynamic understanding of the mechanism of BPA degradation.

Tailoring Macro/Meso/Microporous Structures of Cellophane Noodle-Derived Activated Carbon for Electric Double-Layer Capacitors.

To address the bottleneck associated with the slow ion transport kinetics observed in the porosity of activated carbons (ACs), hierarchically structured pore sizes were introduced on ACs used for electric double-layer capacitors (EDLCs) to promote ion transport kinetics under fast-rate charge-discharge conditions. In this study, we synthesized cellophane noodle-derived activated carbon (CNAC) with tailored porous structures, including the pore volume fraction of macro/meso/micropores and the specific surface area. The porous structures were effectively modulated by adjusting the KOH concentration during chemical activation. In addition, optimized KOH activation in CNAC modulated the chemical bonding ratios of C=O, pyrrolic-N, and graphitic-N. Given the hierarchically designed porous structure and chemical bonding states, the CNAC fabricated with optimized KOH activation exhibited a superior ultrafast rate capability in EDLCs (132.0 F/g at 10 A/g).

KOH-activated hollow carbon spheres with surface functionalization for high-capacity and long-cycle-life lithium-selenium batteries.

Lithium-selenium (Li-Se) batteries are considered promising alternatives to lithium-ion batteries due to their higher volumetric capacity and energy density. However, they still face limitations in efficiently utilizing the active selenium. Here, we develop surface-functionalized mesoporous hollow carbon nanospheres as the selenium host. By using KOH activation, the surface of the carbon nanospheres is functionalized with hydroxyl groups, which greatly improve the utilization of selenium and facilitate the conversion of lithium selenides, leading to much higher capacities compared to ZnCl2 activation and untreated carbon nanospheres. Theory and experimental evidence suggest that surface hydroxyl groups can enhance the reduction conversion of polyselenides to selenides and facilitate the oxidation reaction of selenides to elemental selenium. In-situ and ex-situ characterization techniques provided additional confirmation of the hydroxyl groups electrochemical durability in catalyzing selenium conversion. The meticulously engineered Se cathode demonstrates a high specific capacity of 594 mA h g-1 at 0.5C, excellent rate capability of 464 mA h g-1 at 2C, and a stable cycling performance of 500 cycles at 2C with a capacity retention of 84.8 %, corresponding to an ultra-low-capacity decay rate of 0.0144 % per cycle, surpassing many reported lithium-selenium battery technologies.

Investigations of NO reduction by coal-based activated carbon with KOH activation: Performance and mechanism.

Selective catalytic reduction of ammonia is the most widely used technology for NOx removal, but there have been serious ammonia leaks and a narrow reaction temperature window. To overcome these limitations, a coal-based activated carbon (CAC) approach using KOH activation for the ammonia-free reduction of NO was investigated in this work. A preparation process was investigated by evaluating the De-NOx performance at different mass ratios (KOH:coal = 0-3:1), and activation temperatures (700-900 °C). The optimum conditions were an activation temperature of 700 °C and a 1:1 ratio of KOH/coal, named CAC-1:1-700. Between 330 and 500 °C, the NO conversion efficiency is maintained at 100% within 90 min. The CAC-1:1-700 showed excellent denitrification performance and SO2 resistance. Based on BET, SEM, XRD, Raman, FT-IR, and XPS characterization analysis, it was found showed that KOH activation could increase the amorphous carbon, pore structure, and C(O) functional groups in CAC, which had positive effects on the denitrification performance. Furthermore, the evolution of char structures and surface species before and after the Char-NO-O2 reaction was evaluated by Raman and XPS, and the possible reaction mechanisms was proposed. Aliphatic structures and small aromatic rings can play the same role in De-NOx, O2 is adsorbed on the carbon to form an oxygen-containing functional group, generating more C-O groups and creating reactive sites C*. NO then interacts with these reactive sites and is reduced to N2. This research prepared CAC as a promising potential alternative to ammonia reductants due to its excellent denitration performance over a medium temperature range and complex flue gas environments, while providing the high-value utilization of coal resources.