Preparation of activated carbon from Dipterocarpus alatus fruit and its application for methylene blue adsorption

Activated carbons were prepared from three parts of Dipterocarpus alatus fruit (wing, endocarp and pericarp), an abundant and renewable waste in Southeast Asia, by chemical activation using ZnCl₂, FeCl₃, H₃PO₄ and KOH and physical activation using CO₂ and steam. This study indicated that activated carbon prepared from Dipterocarpus alatus fruit could be employed as a promising adsorbent for the removal of methylene blue from aqueous solution. ZnCl₂ activation led to an activated carbon with a surface area of 843 m² g⁻¹ and was able to remove methylene blue from aqueous solution. Adsorption studies were performed and analysed using Langmuir and Freundlich isotherm equations. Adsorption data demonstrated an excellent fit with the Langmuir isotherm model, with the maximum adsorption capacity of 269.3 mg g⁻¹ at equilibrium. Pseudo-first order and pseudo-second order kinetic models were used in this study to describe the adsorption mechanism. The results show that methylene blue adsorption is pseudo-second order, indicating that liquid film diffusion, intra-particle diffusion and surface adsorption coexisted during methylene blue adsorption on the activated carbon. The activated carbon prepared from Dipterocarpus alatus fruit is a low cost and effective adsorbent with a fast rate for the removal of methylene blue from aqueous solutions when compared with a number of activated carbons studied in the literature.

Activated carbons were prepared from Dipterocarpus alatus fruit by chemical and physical activation and used for the removal of methylene blue from aqueous solution.     

Preparation and optimization of activated nano-carbon production using physical activation by water steam from agricultural wastes

Production of activated nano-carbon from agricultural wastes was studied in this work. To obtain the optimum production conditions by a physical activation method, influence of temperature (850, 900, 950 and 1000 °C), activation residence time (30, 60 and 90 min), and mill rotation (200, 300 and 400 rpm) were investigated using three different raw materials including walnut, almond and pistachio shells. To prepare activated nano-carbon, all the samples were heated up to the final activation temperature under a continuous steam flow of 130 cm³ min⁻¹, and at a heating rate of 3 °C min⁻¹, and were held at the different activation temperatures for 30, 60 and 90 minutes. BET surface area of the obtained activated carbons was measured from nitrogen adsorption data in the relative pressure range between 0 to 1. Activated nano-carbon standard indexes were evaluated according to the ASTM standard and the samples were compared. First, the cellulose raw material was heated in the carbonization furnace at 600 °C and then activated in the advanced activation furnace at a temperature between 850 to 1000 °C for 30, 60 and 90 minutes with water vapor. Ash percentage, iodine content, moisture content, specific area, elemental analysis, and FESEM were used for product characterization. The results of the analysis showed that by using the water vapor physical activation method and optimizing the parameters of this process including time and rotation of the mill up to 10 min and 400 rpm, resulted in a significant increase in specific surface area, cavity volume and the iodine number of the final product.

Production of activated nano-carbon from agricultural wastes was studied in this work.     

Comparative study of the elimination of copper,cadmium, and methylene blue from water by adsorption on the citrus Sinensis peel and its activated carbon

The accumulation of heavy metals and dyes in wastewater is a persistent environmental threat with serious hazards consequences affecting all living organisms. Their removal has become a challenging environmental requirement. Adsorption using agricultural waste is one of the cost-effective removal techniques in which the biomass can be valorized. In this study, two adsorbents were prepared and compared in removing copper, cadmium, and methylene blue from water: citrus Sinensis peel (CP) and its activated carbon (AC). Many physical and chemical properties of the prepared adsorbents were investigated using several techniques. Various operational parameters such as initial adsorbate concentration, contact time, pH, adsorbent mass, and temperature were examined. The optimum uptake of Cd, Cu, and MB was obtained after 2 h contact time by using 0.25 g of adsorbent and 400 mg L⁻¹ metal ions or 100 mg L⁻¹ MB initial concentration at pH 5 (for metal ions only) and temperature of 25 °C. Slight superiority for the CP was seen. Furthermore, isothermal models were resolved in all the studied cases. Unlike for MB, the Langmuir model is more applicable for the adsorption of the cations on both adsorbents with maximum adsorption of 80 mg g⁻¹ of Cd(ii) on CP. Finally, the adsorbents achieved good reuse performance, especially for CP which can be used up to 4 times to remove the metal ions, proving that they are low-cost and environmentally friendly materials able to remove inorganic and organic contaminants from water.

The accumulation of heavy metals and dyes in wastewater is a persistent environmental threat with serious hazards consequences affecting all living organisms. Citrus Sinensis peel and its activated carbon particles effectively remove Cu(ii), Cd(ii), and MB from water.     

Study on the applicability of pressurized physically activated carbon as an adsorbent in adsorption heat pumps

Activated carbon is a suitable adsorbent for adsorption heat pumps (AHPs) with ethanol refrigerants. Although chemically activated carbon with highly developed pore structures exhibits good ethanol adsorption, the associated high production costs inhibit its practical application as an AHP adsorbent. Moreover, although physical activation can produce inexpensive activated carbon, the limited pore development limits the ethanol uptake. Recently, we developed a pressurized physical activation method that can produce activated carbon with a well-developed pore structure and characteristic pore size distribution. In this study, we investigated the applicability of the pressurized physically activated carbon as an adsorbent in activated carbon–ethanol AHP systems. Because of the large number of pressurization-induced pores of appropriate size, the pressurized physically activated carbon showed effective ethanol uptake comparable with that of chemically activated carbon on a weight basis. Furthermore, on a volume basis, the pressurized physically activated carbon, with a high bulk density, showed much higher effective ethanol uptake than chemically activated carbon. These results confirm the potential of the pressurized physically activated carbon as a relatively inexpensive high-performance adsorbent for AHP systems with ethanol refrigerants.

Thanks to the large number of pressurization-induced pores of appropriate size and the high bulk density, the pressurized physically activated carbon showed much higher effective ethanol uptake than chemically activated carbon.     

Agricultural wastes from wheat,barley, flax and grape for the efficient removal of Cd from contaminated water

Agricultural production results in wastes that can be re-used to improve the quality of the environment. This work has investigated for the first time the use of abundant, un-modified agricultural wastes and by-products (AWBs) from grape, wheat, barley and flax production, to reduce the concentration of Cd, a highly toxic and mobile heavy metal, in contaminated water. At concentrations of 1.1 mg Cd per L, flax and grape waste were found superior in removing Cd compared with a granular activated carbon used in water treatment, which is both more expensive and entails greater CO₂ emissions in its production. At a pH representative of mine effluents, where Cd presents its greatest mobility and risk as a pollutant, grape and flax waste showed capacity for effective bulk water treatment due to rapid removal kinetics and moderate adsorption properties: reaching equilibrium within 183 and 8 min – adsorption capacities were determined as 3.99 and 3.36 mg Cd per g, respectively. The capacity to clean contaminated effluents was not correlated with the surface area of the biosorbents. Surface chemistry analysis indicated that Cd removal is associated with exchange with Ca, and chemisorption involving CdCO₃, CdS and CdO groups. This work indicates that some AWBs can be directly (i.e. without pre-treatment or modification) used in bulk to remediate effluents contaminated with heavy metals, without requiring further cost or energy input, making them potentially suitable for low-cost treatment of persistent (e.g. via mine drainage) or acute (e.g. spillages) discharges in rural and other areas.

Agricultural production results in wastes that can be re-used to improve the quality of the environment.     

Broadening the pore size of coal-based activated carbon via a washing-free chem-physical activation method for high-capacity dye adsorption

Aiming to overcome the limitations of the narrow pore size distributions of traditional activated carbon materials and to achieve wide adaptabilities towards large molecules adsorption, we herein demonstrate a new type of activated carbon with a broadened pore size distribution for high-rate and high-capacity aqueous dye molecule (Rhodamine B) adsorption. The preparation of CP-AC is achieved by a facile and one-step mineral-assisted chem-physical activation strategy from Chinese large-reserve Zhundong coal with ZnCl₂ and CO₂ as the activation agents. The method yields the activated carbon (CP-AC) that has a pore-size broadened hierarchical pore configuration with a high surface area and a large pore volume, favorably enabling a high-capacity Rhodamine B adsorption up to 881 mg g⁻¹, which is among the highest levels of the reported activated carbons. A sonication-assisted adsorption test further demonstrates the high-rate adsorption capability of CP-AC with Rhodamine B adsorption capacity up to 842 mg g⁻¹ within 30 min (96% of the saturation capacity) while microporous activated carbon obtained by solely ZnCl₂ activation could just achieve a capacity of 374 mg g⁻¹ within 30 min. In virtue of the low-cost resource materials and washing-free craft, this work offers a simple and green preparation strategy towards high-performance coal based activated carbons, holding great potentials for the industrial production and applications.

Aiming to overcome the limitations of the narrow pore size distributions of traditional activated carbon, we demonstrate a new type of activated carbon with a broadened pore size distribution for high-rate and high-capacity aqueous dye adsorption.     

Metal-free high-adsorption-capacity adsorbent derived from spent coffee grounds for methylene blue

Heavy-metal-free carbon materials were prepared from spent coffee grounds (SCG) using the coupled KOH–urea and NaOH–urea as activating agents, and these were compared with SCG activation by the alkali salts alone. SCG was impregnated with the activating agents before being pyrolyzed at 800 °C under a N₂ atmosphere. Characterization of the as-pyrolyzed carbon materials was performed by field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and measurement of N₂ adsorption–desorption isotherms. The carbon materials were utilized for the adsorption of methylene blue (MB) in aqueous solutions. Combining KOH and urea as activating agents resulted in the generation of pertinent SCG-derived carbon material properties, including a large surface area (1665.45 m² g⁻¹) and excellent MB adsorption capacity. Adsorption efficiencies were studied using adsorption kinetics (pseudo-first-order and pseudo-second-order) and adsorption isotherm (Langmuir, Freundlich, and Temkin) models. The influences of pH and temperature were investigated. The results of this work raise new possibilities for synthesizing carbon materials with high MB adsorption capacities from biowastes, via less-toxic, energy-saving conventional pyrolysis methods for water-treatment applications.

Spent coffee grounds derived carbon was prepared for the adsorption of methylene blue in aqueous solutions.     

Converting waste textiles into highly effective sorbent materials

Activated carbon fibres with a tubular structure and exfoliated surface were produced utilizing cotton textile waste as the precursor. The synthesized carbon fibres were freeze dried resulting in a tubular structure and large pore size distribution. The absorption properties against various oils and organic solvents were accessed, these fibres showed some of the highest absorption capabilities reported for cellulose based carbons, in particular for olive oil, gasoline and chloroform.

Activated carbon fibres with a tubular structure and exfoliated surface were produced utilizing cotton textile waste as the precursor.     

High-efficiency adsorption and regeneration of methylene blue and aniline onto activated carbon from waste edible fungus residue and its possible mechanism

Edible fungus residue as an efficient and low-cost precursor was used to produce Edible Fungus residue Activated Carbon (EFAC) using the zinc chloride activation method at a 1 : 2 impregnation ratio and 600 °C activation for 3 hours. The activation process does not need gases like nitrogen and is suitable for mass production. Fungal biodegradation facilitates efficient chemical activation, which might have generated abundant pores on the activated carbon sample. Using BET, X-ray diffraction (XRD), scanning electron microscopy (SEM), and FTIR characterization, reveals that EFAC exhibits a large specific surface area (1070 m² g⁻¹), and large pore volume (0.68 cm³ g⁻¹), with its surface displaying a honeycomb-like structure. The EFAC adsorbs methylene blue (MB) and aniline in water, with maximum adsorptions of 662.25 and 27.10 mg g⁻¹, respectively. Various adsorption conditions, such as the EFAC dosage, pH, contact time and initial concentration were investigated. The adsorption is characterized by the pseudo-second-order kinetic and Langmuir isotherm models, with thermodynamics studies indicating that the adsorption is endothermic and spontaneous. Furthermore, the EFAC exhibited good regeneration performance by a 90% ethanol solution. The EFAC is a low-cost and environmentally friendly adsorbent for removing organic contaminants in wastewater.

Edible fungus residue as an efficient and low-cost precursor was used to produce Edible Fungus residue Activated Carbon (EFAC) using the zinc chloride activation method at a 1 : 2 impregnation ratio and 600 °C activation for 3 hours.     

Chitosan-derived three-dimensional porous carbon for fast removal of methylene blue from wastewater

Despite much progress in modifying chitosan as an absorbent for wastewater treatment, it is still difficult for current chitosan-based adsorbents to achieve the desired removal effects towards basic dyes. In this study, chitosan-derived three-dimensional porous carbon (CTC) consisting of large-diameter channels and mesopores was prepared to remove methylene blue (MB) from wastewater. The results indicate that CTC has excellent performance for MB removal, and the maximum adsorption capacity was 925.93 mg g⁻¹ at 318 K. The adsorption isotherm and kinetics models of MB on CTC could be described well by the Langmuir isotherms and the pseudo-second-order rate model. An experiment to study the CTC removal of MB from a flowing aqueous solution was performed using a homemade device. The water treatment rate of CTC reached 250 L g⁻¹ h⁻¹, with high MB removal efficiency (>93.4%). Furthermore, the desorption–adsorption experiments indicate that CTC is also a reusable adsorbent that can be applied to recover MB from wastewater. The obtained CTC is a promising alternative for the current expensive absorbents and provides a concept for designing the three-dimensional (3D) structures of raw materials to improve adsorption capability.

The chitosan-derived three-dimensional porous carbon (CTC) consisting of large-diameter channels and mesopores was prepared by two steps activation and used for the removal of methylene blue (MB) from wastewater.     

Degradation of methylene blue by dielectric barrier discharge plasma coupled with activated carbon supported on polyurethane foam

The degradation of methylene blue (MB) using a novel dielectric barrier discharge plasma reactor coupled with activated carbon supported polyurethane foam (AC/PUF) was investigated in this paper. The plasma reactor combining a glass bead-packed bed and a microporous plate was developed. The AC/PUF provided sufficient contact area between carbon media and pollutants and hence revealed a good MB removal capacity. The effects of input voltage and initial MB solution concentration on MB degradation efficiency were examined. Kinetic study indicated that plasma and AC/PUF in the coupled system had a good synergistic effect in MB degradation. The degradation efficiency of 100 ppm MB solution could reach 97.9% with 10 min treatment in the coupled system, which was close to that obtained by plasma treatment alone for 30 min (97.5%). The COD removal in the plasma and AC/PUF coupled system (90.7%) was much higher than that obtained by plasma treatment followed by AC/PUF adsorption (58.3%). In addition, the energy yield (G₅₀) of the coupled system was up to 38.3 g kW⁻¹ h⁻¹, suggesting great energy efficiency of the system. Moreover, repeated use experiments of AC/PUF showed the good utilization potential of the coupled system. Finally, a possible degradation pathway of MB was proposed.

High dye degradation efficiency, COD removal and energy yield were obtained using a novel plasma reactor coupled with AC/PUF.     

Coconut-based activated carbon fibers for efficient adsorption of various organic dyes

In this study, using coconut fibers as raw material, activated carbon fibers were prepared via carbonization and KOH activation processes. The morphology, composition, specific surface area, pore structure and thermal stability of the resulting activated carbon fibers were systematically characterized. It was found that the activation process increases the specific surface area of carbon fibers to a greater extent via formation of a large number of micropores (0.7–1.8 nm) and a certain amount of slit-shaped mesopores (2–9 nm). The specific surface area and the pore volume of the activated carbon fibers reach 1556 m² g⁻¹ and 0.72 cm³ g⁻¹, respectively. The activation process can also decompose the tar deposits formed after the carbonization process by pyrolysis, making the surface of the activated carbon fibers smoother. To study the adsorption properties of the as-prepared activated carbon fibers, the adsorption capacities and adsorption kinetics of various organic dyes including methylene blue, Congo red and neutral red were investigated. The adsorption capacities of the dyes increased with the increasing initial dye concentrations, and varied greatly with the pH value of the system. In methylene blue and neutral red systems, the adsorption capacities reach the maximum at pH 9, and in the Congo red system, it reaches the maximum at pH 3. The adsorption capacities of the activated carbon fibers in methylene blue, Congo red and neutral red systems reached equilibrium at 150, 120, and 120 min, and the maximum adsorption capacities were 21.3, 22.1, and 20.7 mg g⁻¹, respectively. The kinetics of the adsorption process was investigated using three models including pseudo-first-order, pseudo-second-order and intraparticle diffusion models. The results indicated that the dynamic adsorption processes of coconut-based activated carbon fibers to methylene blue, Congo red and neutral red were all in accordance with the second-order kinetic model, and the equations are as follows: t/Q_t = 0.1028 + t/21.3220, t/Q_t = 0.1128 + t/21.5982 and t/Q_t = 0.0210 + t/20.6612.

Activated carbon fibers with high micropore volume and large specific surface area were prepared from abundant and low-cost coconut fibers, which show excellent adsorption performances towards various dyes.     

Air activation of charcoal monoliths for capacitive energy storage

Charcoal monoliths derived from waste wood were activated with air for the application of electrochemical capacitor electrodes and an insight was given into the activation mechanism. The mild air activation is effective and pollution-free compared to the common chemical activation using KOH etc. for the preparation of crack-free carbon monoliths. The activation process was controlled by altering the activation temperature and time, and their effects on the nanostructure of charcoal monoliths were studied. As the activation temperature or time increased, air eroded the defective surface of charcoal layer-by-layer, with the oxygen atoms being introduced by chemisorption and oxidation reactions and removed by dehydration and decomposition reactions. Meanwhile, micro-pores were produced. The electrode activated at 300 °C for 1 h, with a specific surface area of 567 m² g⁻¹ and a high micro-porosity of 86%, exhibited a specific capacitance of 203 F g⁻¹ and 35.5 F cm⁻³. Moreover, it presented a higher total capacitance of 3.6 F cm⁻² than most reported pellet electrodes. These findings give a reasonable picture of the air activation process and are instructive to prepare activated carbon monoliths under an oxidizing environment.

Charcoal monoliths derived from waste wood were activated with air for the application of electrochemical capacitor electrodes and an insight was given into the activation mechanism.     

Fast removal of methylene blue from aqueous solution using coal-based activated carbon

Coal-based activated carbons (CACs) were prepared from three long flame coals with different ash and volatile matter content. CACs prepared by coal with high ash (6.74%) and volatile matter content (34.31%) showed better adsorption efficiency towards MB (547.35 mg g⁻¹) due to higher surface area and pore volume. The effect of coal to activating agent ratio (CAR) was also investigated in a batch reactor. The porosity development is closely related to the CAR. The calculated monolayer adsorption amount (714.29 mg g⁻¹) was found on YLC-AC-3 with a surface area of 1212.50 m² g⁻¹. The equilibrium data were favorably described by the Langmuir and Freundlich isotherm models, and adsorption kinetics fitted well to the pseudo-second order model. The removal efficiency remains at 98.21% after five runs. The results of the present study suggest that CACs are potential and effective adsorbents in fast removal of dyes from aqueous solution.

A monolayer adsorption amount of MB (714.29 mg g⁻¹) was found on a coal-based activated carbon prepared by a simple method.     

Adsorption of methylene blue and tetracycline onto biomass-based material prepared by sulfuric acid reflux

The adsorptive removal of environmental pollutants is an effective method for the treatment of contaminated water. Thus, the preparation of adsorbents from low-cost, readily available, and renewable resources has garnered immense attention in recent years. In this study, a facile one-step method for the preparation of a high-capacity adsorbent is demonstrated by refluxing pine cones in concentrated sulfuric acid. With sulfuric acid reflux, the pine cones undergone carbonization as well as functionalization with sulfonic acid groups. The adsorbent demonstrated high adsorption capacity for two emerging organic pollutants, methylene blue (MB) and tetracycline (TC). Different variables such as pH, temperature, contact time, and initial concentration of the pollutants were analyzed and showed that the adsorption capacity for MB increased in a basic pH and vice versa for TC. Also, the elevated temperature favored the adsorption for both MB and TC. The maximum adsorption capacity was found to be 1666.66, and 357.14 mg g⁻¹ for MB and TC, respectively. In comparison to the pristine pine cone, the sulfuric acid treated pine cone demonstrated an extraordinary improvement in the adsorption capacity. The adsorption of MB and TC was performed from the tap water matrix and similar adsorption capacities were found. A packed glass column was also prepared to demonstrate the adsorption of MB from tap water under flow conditions.

Facile conversion of pine cones into a high-capacity adsorbent for the removal of methylene blue and tetracycline from water.     

A study on the preparation of pitch-based high-strength columnar activated carbon and mechanism of phenol adsorption from aqueous solution

Coal tar pitch was ground into powder and hydroformed with high pressure. After pre-oxidation, the pitch was activated by CO₂ at high temperature. The effects of different preparation conditions on the yield, pore structure and phenol adsorption capacity of activated carbon were investigated, and activated carbon prepared under suitable conditions had good adsorption performance. A pore volume of 1–10 nm is the main absorption structure according to the analysis of pore size distribution and phenol adsorption capacity. The activated carbon showed high mechanical strength through compressive strength tests. Graphite nanocrystals around 5 nm were observed in the TEM images, and it illustrates that grain refinement results in the high strength. These nanocrystal stacked structures are easier to make and enlarge pores by activation than graphite layer stacked structures. Surface functional groups are considered not to be the active sites of phenol adsorption as suggested by the results of FTIR and Boehm''s titration, and acidic oxygen-containing functional groups are harmful to phenol adsorption, which happen to be removed in the reductive preparation atmosphere. The donor–acceptor complex mechanism can be ruled out, and the π–π interactions are considered the most likely mechanism. The Langmuir and Redlich–Peterson models are better fitted to the adsorption isotherms. Adsorption kinetics fit the intraparticle diffusion model best. Comparison of different activated carbons shows that suitable pore size is important for phenol adsorption. Thermodynamic parameters demonstrate that the adsorption process is spontaneous and exothermic, and the entropy increases. Pitch-based high-strength columnar activated carbon is an effective and low cost adsorbent for phenol wastewater treatment. This carbon nanocrystal material also provides a new direction for catalyst carriers.

Coal tar pitch was ground into powder and hydroformed with high pressure. After pre-oxidation, the pitch was activated by CO₂ at high temperature.     

Silkworm cocoon derived N,O-codoped hierarchical porous carbon with ultrahigh specific surface area for efficient capture of methylene blue with exceptionally high uptake: kinetics,isotherm, and thermodynamics

Dyes are typical water contaminants that seriously affect water quality. In this study, silkworm cocoon derived N, O-codoped hierarchical porous carbon was successively developed via a facile pre-carbonization and chemical activation method, and characterized thoroughly by SEM, TEM, HRTEM, XRD, Raman, N₂ adsorption and XPS. The as-prepared N, O-HPC showed a well-developed porous structure with an ultra-high specific surface area of 2270.19 m² g⁻¹, which proved to be a high-efficiency adsorbent. Batch adsorption experiments demonstrated that MB adsorption was highly dependent on contact time, initial MB concentration, temperature and initial solution pH. However, no remarkable effects of humic acid and ionic strength were observed. In the kinetic studies, the good applicability of a pseudo-second-order kinetic model was demonstrated. The adsorption isotherm study showed that a Langmuir isotherm model can describe the experimental data much more suitably with a maximum monolayer adsorption capacity value of 2104.29 mg g⁻¹, which is among the highest in previously reported adsorbents and ascribed to multiple adsorption mechanisms including pore filling, π–π stacking interaction and electrostatic interaction between MB and N, O-HPC. Thermodynamic analyses suggested that MB adsorption onto N, O-HPC was spontaneous and endothermic. Furthermore, the as prepared adsorbent showed highly efficient adsorption for MB in tap water and synergistic adsorption performance toward MB and MO. Therefore, N, O-HPC derived from silkworm cocoon could be considered as an efficient, novel and advantageous material for wastewater remediation.

Silkworm cocoon derived N, O-HPC (S_BET = 2270.19 m² g⁻¹) was synthesized, and demonstrated exceptionally high uptake of MB (2104.29 mg g⁻¹).     

Low-cost Y-type zeolite/carbon porous composite from coal gasification fine slag and its application in the phenol removal from wastewater: fabrication,characterization, equilibrium,and kinetic studies

As an industrial solid waste, coal gasification fine slag (CGFS), which consists of many elements, such as silicon, aluminum, and carbon, could be used as an important resource. Therefore, this solid waste was used as a raw material to prepare high-value-added adsorption material for the treatment of industrial wastewater in this study. A hydrothermal synthesis method was applied to convert CGFS into a Y-type zeolite/carbon porous composite. The effects of time and temperature on the synthesis were studied. XRD, SEM, and other techniques were used to analyze the material and its physicochemical properties. Additionally, the adsorption performance of the material for phenol was studied. The results showed that the composite has better adsorption capacity for phenol than CGFS. The Freundlich model and pseudo-second-order kinetics well fitted the adsorption behavior of the composite, which demonstrated that the adsorption of phenol was dominated by chemical adsorption.

A method is presented for preparing a Y-type zeolite/carbon composite with coal gasification fine slag for removing phenol in wastewater.     

Preparation and electrochemical performance of nitrogen-enriched activated carbon derived from silkworm pupae waste

In this study, nitrogen-enriched activated carbon from silkworm pupae waste (P-AC) was successfully prepared and its electrochemical performances in aqueous and organic electrolytes were investigated. Silkworm pupae waste is beneficial because it is a nitrogen-enriched, inexpensive, and locally available material. The preparation process includes hydrothermal treatment of the silkworm pupae waste at 200 °C, and chemical activation using zinc chloride at activation temperatures of 700, 800 and 900 °C (P700, P800, and P900, respectively). The nitrogen content in the P-ACs was approximately 3.8–6.4 at%, decreasing with activation temperature, while the surface area was approximately 1062–1267 m² g⁻¹, increasing with activation temperature. Compared to a commercial AC, the P-ACs show higher nitrogen content but lower surface area. Furthermore, the P800 exhibited superior specific capacitance (154.6 and 91.6 F g⁻¹ in aqueous and organic electrolytes) compared to a commercial AC despite possessing smaller surface area. The high nitrogen content enhanced the pseudocapacitance and improved the electrical conductivity of the P-ACs. These properties were confirmed by relatively low series and charge transfer resistances, a capacity retention higher than 88% at a current density of 0.5 A g⁻¹ and excellent cycling stability demonstrated by maintaining 97.6% of its capacitance after 3000 cycles. These results demonstrate that silkworm pupae waste is a viable source of nitrogen-enriched AC for application in supercapacitors.

Nitrogen-enriched activated carbon from silkworm pupae prepared by hydrothermal treatment and chemical activation exhibited superior specific capacitance with excellent cycling stability.     

Removal of methylene blue from aqueous solution by cattle manure-derived low temperature biochar

Biochar is a low cost and renewable adsorbent which can be used to remove dye from wastewater. Cattle manure-derived low temperature biochar (CMB) was studied to remove methylene blue (MB) from aqueous solution in this paper. The effect of factors including initial concentration of MB, dosage, contact time, and pH on the adsorption properties of MB onto biochar were studied. Characterization of the CMB and MB adsorbed on CMB was performed using techniques including BET, FTIR and SEM. The adsorption isotherm, kinetics, thermodynamics and mechanism were also studied. The results showed the equilibrium data were well fitted to the Langmuir isotherm model, and the saturation adsorption capacity of CMB₂₀₀ was 241.99 mg g⁻¹. Pseudo-second order kinetics was the most suitable model for describing the adsorption of MB onto biochar. The adsorption thermodynamics of MB on biochar showed that the adsorption was a spontaneous and endothermic process. Through zeta potential measurement, Boehm titration, cation exchange, deashing and esterification experiments, the importance of ash to adsorption was verified, as well as the adsorption mechanism. The adsorption mechanism of MB on CMB₂₀₀ involved cation exchange, electrostatic interaction, hydrogen bonding, physical effects and others. This work shows that CMB₂₀₀ holds promise to act as an effective adsorbent to remove MB in wastewater.

Biochar is a kind of low cost and renewable adsorbents which can be used to remove dye from wastewater. The mechanism between MB and CMB involved cation exchange, electrostatic interaction, hydrogen bonding, physical function and others.