Moso bamboo, as a kind of renewable functional material, exhibits outstanding development potential. It is promising to prepare activated carbon with good mechanical strength and high specific surface area using moso bamboo as raw material. In this work, we employed a hydraulic extruder to extrude the bamboo charcoal and the adhesive to obtain the moso bamboo activated carbon, and improved the specific surface area of the columnar activated carbon through high-temperature water vapor activation. Through the catalytic role of the water vapor activation process, the formation and expansion of the pores were promoted and the internal pores were greatly increased. The obtained columnar activated carbon shows excellent mechanical strength (93%) and high specific surface area (791.54 m2/ g). Polyacrylamide@asphalt is one of the most effective adhesives in the high-temperature water vapor activation. The average pore size (22.99 nm) and pore volume (0.36 cm3/ g) of the prepared columnar activated carbon showed a high mesoporous ratio (83%). Based on the excellent pore structure brought by the activation process, the adsorption capacity of iodine (1135.75 mg/g), methylene blue (230 mg/g) and carbon tetrachloride (64.03 mg/g) were greatly improved. The resultant moso bamboo columnar activated carbon with high specific surface area, excellent mechanical properties, and outstanding adsorption capacity possesses a wide range of industrial applications and environmental protection potential.

We produced an activated carbon using sodium-lignosulfonate, in which we investigated how the sodium salt in lignin served as the activating agent during heat treatment. Our process resulted in a product with a high specific surface area of 1324 m2/ g at 800 °C and microporous structure. During the activation process, we observed the consumption of carbon due to the dehydration reaction of NaOH and the reduction of Na2CO3 to metallic Na, which created pores through oxidation/ reduction reactions. The intercalation of metallic Na between the lattices at high temperatures formed additional pores and increased the specific surface area. Our proposed mechanism holds promise for enhancing the control of the microstructure and porosity of activated carbons through the thermal treatment of biomass.

Enhancing the capacitive deionization performance requires the inner structure expansion of porous activated carbon to facilitate the charge storage and electrolyte penetration. This work aimed to modify the porosity of coconut-shell activated carbon (AC) through CO2 activation at high temperature. The electrochemical performance of CO2- activated AC electrodes was evaluated by cyclic voltammetry, charge/discharge test and electrochemical impedance spectroscopy, which exhibited that AC-800 had the superior performance with the highest capacitance of 112 F/g at the rate of 0.1 A/g and could operate for up to 4000 cycles. Furthermore, in the capacitive deionization, AC-800 showed salt removal of 9.15 mg/g with a high absorption rate of 2.8 mg/g min and Ni(II) removal of 5.32 mg/g with a rate close to 1 mg/g.min. The results promote the potential application of CO2- activated AC for desalination as well as Ni-removal through capacitance deionization (CDI) technology.

The pitch-based activated carbon fibers (ACFs) were prepared from ethylene tar-derived pitches containing nickelocene (CNi) or nickel nitrate (NiN). The effects of different anions and contents of metal salts on the microstructure and surface chemical properties of fibers were investigated. The results revealed that Ni2+ from CNi mainly remained its pristine molecule in the organometal salt-derived pitch (OP-xCNi), while Ni2+ from NiN occurred complexation reaction with polycyclic aromatic hydrocarbons (PAHs) in the inorganic metal salt-derived pitch (IP-xNiN) due to the weaker binding ability between anions and Ni2+ of CNi than CNi. The XRD and SEM results confirmed that IP-3NiN-ACF contained Ni, NiO, Ni2O3 nanoparticles with different size distributions, while OP-3CNi-ACF only contained more uniformly distributed Ni nanoparticles with small size. Furthermore, OP-3.0CNi-ACF presented higher specific surface area of 1862 m2/ g and a pore volume of 1.69 cm3/ g than those of IP-3.0NiN-ACF due to the formation of pore structure during the in-situ catalytic activation of different metal nanoparticles. Therefore, this work further pointed out that the desired pore structure and surface chemistry of pitch-based ACFs could be obtained through regulating and controlling the interaction of anion species, metal cations and PAHs during the synthesis of pitch precursors.

In this work, the sulfonic acid group was introduced into the resorcinol–formaldehyde (RF) microspheres by the addition of p-phenolsulfonic acid during the polycondensation process of RF. The hydrophilicity of the sulfonated RF allowed KOH to infiltrate inside the microspheres, which enhanced the formation of mesopores in the carbon microspheres during the activation process by KOH. SEM and TEM observations and N2 adsorption measurements verified the formation of abundant mesopores in the porous carbon microspheres. The BET surface area of these mesoporous carbons exceeded 2000 m2/ g. In 17 m NaClO4 “water-in-salt” (WIS) electrolyte-based supercapacitor, the synthesized mesoporous carbon exhibited high specific capacitance of 170 F/g at current density of 0.5 A/g, comparable to those in regular KOH electrolyte. When graphite was used as current collectors, the symmetric cell could operate at 2.5 V, and the mesoporous carbon exhibited an energy density of 43 Wh/kg at power density of 0.25 kW/kg, and 25 Wh/kg at power density of 6.25 kW/kg, respectively, which were superior to those using Pt or stainless steel as current collectors. The mesoporous carbon/graphite was an excellent electrode in new-generation “WIS” electrolyte-based high-voltage supercapacitor due to their high energy and power density.

This research aims to study the effect of impregnation ratio and activation temperature on microporous development of activated carbon (AC). Rubberwood chips, which are wasted from home furnishing industry, were used as precursors for synthesized of activated carbon by chemical activation employing Potassium hydroxide (KOH) as activation agent. Rubberwood char was carbonized at 400 °C for 1 h under inert gas. In this experiment, the rubberwood chars were impregnated with KOH solution by 1:1–3 (char: KOH) impregnation ratio for 24 h, then the samples were activation at 600–800 °C. Surface area, pore volume, micropore volume, pore size distribution, adsorption isotherm and porous structure were analyzed in this experiment to identify the properties of derived activated carbon. According to the investigation, the activated carbon, activated at 800 °C with impregnation ratio of 1:3, demonstrated the highest surface area, pore volume and micropore volume as 1491.75 m2/g, 0.6777 cm3/g, and 0.5813 cm3/g, respectively. Its average pore size was 1.82 nm and it also showed type I adsorption isotherm which indicates as microporous solid.

Biomass of agricultural waste is getting increasing attention all over the world as it is a kind of renewable, abundantly available, low cost, and environmentally friendly resource. Preparation of activated carbon from agricultural waste via microwave-assisted chemical agent activation. The porosity, surface area, and functional and surface chemistry were featured by means of low-temperature nitrogen adsorption, Scanning Electron Microscopy, (SEM) and Fourier Transform Infrared Spectroscopy (FTIR). The best conditions resulted in activated carbon with adsorption capacity of 517.5 mg/g and carbon yield of 80.99%. The activated carbons from carbonized tobacco stem with K2CO3 activation by microwave radiation is highest of surface area, and total pore volume corresponded to 2557 m2/g, and 1.647 cm3/g, respectively, with a high contribution of mesopores, microwave power of 700 W, and irradiation time of 30 min. The results of the review showed that chemical activation could develop both microporosity and mesoporosity. The findings support the potential to prepare high surface area and micropore-activated carbon from agricultural waste by microwave-induced chemical activation.

Preparation of activated carbon from biomass residue with conventional steam activation was conducted to find the alternative raw materials for meeting the high demand for low-cost porous material in the desiccant application. In this study, activated carbons were produced from dead camphor leaves using two-step methods at different preparation temperatures. The characterization results revealed that the prepared activated carbons have a surface area of 700 m2/g, with 75% of microporosity. The water vapor sorption study reported that the water uptake of camphor leaf-based activated carbons was strongly affected by the pore properties of the materials. Moreover, from the water adsorption kinetics, it was observed that the rate constant of adsorption was varied at each relative pressure, which can be assumed that the water adsorption mechanism is different at each relative pressure. From these results, it was revealed that the prepared camphor leaf-based activated carbons have a promising ability to adsorb water vapor from humid air.

A carbon nanofiber was produced from the Areca catechu husk as a supercapacitor electrode, utilizing a chemical activation of potassium hydroxide (KOH) at different concentrations. One-stage integrated pyrolysis both carbonization and physical activation were employed for directly converting biomass to activated carbon nanofiber. The morphology structure, specific surface area, pore structure characteristic, crystallinity, and surface compound were characterized to evaluate the influence on electrochemical performance. The electrochemical performance of the supercapacitor was measured using cyclic voltammetry (CV) through a symmetrical system in 1 M H2SO4. The results show that the KOH-assisted or absence activation converts activated carbon from aggregate into a unique structure of nanofiber. The optimized carbon nanofiber showed the large specific surface area of 838.64 m2 g−1 with the total pore volume of 0.448 cm3 g−1, for enhancing electrochemical performance. Beneficial form its unique structural advantages, the optimized carbon nanofiber exhibits high electrochemical performance, including a specific capacitance of 181.96 F g−1 and maximum energy density of 25.27 Wh kg−1 for the power density of 91.07 W kg−1. This study examines a facile conventional route for producing carbon nanofiber from biomass Areca catechu husk in economical and efficient for electrode supercapacitor.

The simultaneous use of KOH and nitrogen to manufacture carbon materials provides these materials with properties that the presence of only one of these additives would not give them, such as high porosity and reactivity. However, it is difficult to obtain nitrogen-doped carbon materials with both high porosity and high nitrogen content, as the KOH significantly reduces the nitrogen content. In this review the complex relationships between nitrogen content and nitrogen precursor amount, KOH amount and the activation temperature are discussed, with a focus on the different N-functional groups and the porosity of the fabricated carbons. Generally, increasing activation temperature and increasing KOH amount decrease the nitrogen content due to reactions with the N-containing substructures of carbon, resulting in the release of nitrogen as N2, HCN and other N gases. Increasing these parameters can also result in the reduction of pyridine-N while the amount of quaternary-N increases simultaneously. Besides this, an increase in the amount of nitrogen precursor leads to an increase in the porosity of N-doped materials. However, too high amounts of the nitrogen precursor generate an excess of nitrogen which blocks the pore system and consequently reduces the porosity of the doped carbons.

To meet the increased performance and cost requirements of commercial supercapacitor, a N and O self-doped hierarchical porous carbon is fabricated via a green and simple self-activation route utilizing leaves of wild hollyhock as raw materials. Comparing to commercial activated carbon, the reported material exhibits some marked merits, such as simple and green fabrication process, low cost, and superior capacitance performance. The specific surface area of the obtained N and O codoped hierarchical porous carbon arrives 954 m2 g−1, and the content of the self-doped nitrogen and oxygen reaches 2.64 at.% and 7.38 at.%, respectively. The specific capacitance of the obtained material reaches 226 F g− 1 while the specific capacitance of the symmetric supercapacitor arrives 47.3 F g− 1. Meanwhile, more than 90.3% of initial specific capacitance is kept under a current density of 20 A g− 1, and no arresting degradation is observed for capacitance after 5000 times cycle, perfectly demonstrating the excellent cycle and rate capability of the obtained material. The obtained N and O co-doped hierarchical porous carbon are expected to be an ideal substitution for commercial activated carbon.

In this study, hair waste was converted into active carbon for the first time and its characteristics were analyzed. As chemical activation tool, zinc chloride ( ZnCl2) was impregnated and then carbonized under different temperatures (250–300 °C). Scanning Electron Microscope (SEM) images showed an increase in the pore density, radius and volume of pores. X-ray diffraction analysis (XRD) showed that the samples had an amorphous structure. In Fourier-transform infrared (FT-IR) spectroscope analysis, C=C and N–H vibrations observed in 1515–1520 cm−1 wave number of protein molecules were found to disappear with the increase in temperature. With Raman spectroscopy, the behaviors of D peak at 1344 cm−1 wave number and G peak at 1566 cm−1 wave number expressing structure layout in carbonized structures were analyzed depending on the temperatures. Between these intensities, (ID/IG) the rate was found to differ in direct proportion to temperature. XRD spectrums showed that the samples are converted into a more irregular crystal structure. All these results implied that the waste hair mass could be used as an adsorbant material.

Low thermal conductivity carbon fibers from polyacrylonitrile (PAN) are currently being explored as an alternative for traditional rayon-based carbon fibers with a thermal conductivity of 4 W/m K. Compared to multiple component electrospinning, this research demonstrated another feasible way to make low thermal conductivity carbon fibrous material by electrospinning PAN followed by carbonization and alkali activation. The effects of activation condition on microstructure, pore formation, and thermal conductivity of the resultant carbon nanofibrous material were investigated. The processing-structure-thermal conductivity relationship was revealed and mechanism of thermal conductivity reduction was discussed. The overall thermal conductivity of the prepared carbon nanofibrous material is a result of combined effects from factors of carbon structure and number of pores rather than volume of pores or specific surface area. The activated carbon nanofibrous materials showed thermal conductivity as low as 0.12 W/m K, which is a reduction of ~ 99% when compared to that of solid carbon film and a reduction of ~ 95% when compared to that of carbon nanofibrous material before activation.

A highly functional, environmentally friendly carbonaceous adsorbent material using black liquor (a by-product from the pulp manufacturing) was produced and characterized. This study showed the effect of self-chemical activation driven by inherent alkali, originated from the unique composition of black liquor. A preparation of the micropore-dominant activated carbon was made in an easy and simple manner. The specific surface areas of samples were found to be 718–1591 m2/ g variated upon heat treatment conditions. The sample activated at 850 °C (50 min as retention time) showed the maximum specific surface area of 1591 m2/ g with 13.6% as a production yield. Considering the factors influencing pore structure of activated carbon materials in this study, it was confirmed that mesopore-related surface area increased gradually as the activation temperature and retention time increased. It is noteworthy to address that economically valuable micropore-dominant activated carbon can be produced by a simple heat treatment of the waste material, black liquor. The activated carbon sample derived from black liquor can be applied to various fields, such as environment and energy storage.

The root of Paeonia lactiflora has been used in Chinese medicine. We conducted to check the comparative qualities of ethanol solvent extraction (PLE) and supercritical carbon dioxide extraction (PLS) of P. lactiflora root. PLE had higher antioxidant and polyphenol contents than PLS. But, PLS were significantly increased peroxisome proliferator-activated receptor (PPAR)-α. In addition, PLS inhibited the adipocyte differentiation of 3T3-L1 cells. When treated with the extract at a concentration of 100 μg/mL, the Wnt/β-catenin pathway reporter luciferase activity of HEK 293-TOP cells increased approximately by 3-folds compared to that of the untreated control group. These results indicate that P. lactiflora supercritical carbon dioxide extract may serve as a cosmeceutical for improving skin barrier function and the treatment of obesity.

Energy and environmental are always two major challenges for the sustainable development of the modern human being. For avoiding the serious environmental pollution caused in the fabrication process of porous carbon, a popular energy storage material, we reported a facile, green and activating agent free route hereby directly carbonizing a special biomass, Glebionis coronaria. A nitrogen doped hierarchical porous carbon with a specific surface area of up to 1007 m2 g−1 and a N doping content of up to 2.65 at.% was facilely fabricated by employing the above route. Benefiting from the peculiarly hierarchical porous morphology, enhanced wettability and improved conductivity, the obtained material exhibits superior capacitance performance, which capacitance reaches up to 205 F g−1 under two-electrode configuration, and no capacitance loss is observed after 5000 cycles. Meanwhile, the capacitance retention of the obtained material arrives up to 95.0% even under a high current density of 20 A g−1, illuminating its excellent rate capability. The fabricated nitrogen-doped hierarchical porous carbon with larger capacitance than commercial activated carbon, excellent rate capability and cycle stability is an ideal cost-efficient substitution of commercial activated carbon for supercapacitor application.

To prepare activated carbon with a high specific surface area, oxygen functional groups (OFGs) that can serve as useful electron donors during KOH activation were treated with nitric acid and incorporated into activated carbon. OFGs are incorporated differently according to the surface characteristics of starting materials. Up to 22.46% OFGs are incorporated into wood-based activated carbons (WACs), the C=O, COOH contents was 1.90, 17.05%, respectively. Whereas up to 12.82% OFGs are incorporated into coconut shell-based activated carbons, the C=O, COOH contents was 4.12, 6.15%, respectively. The OFGs used for increasing the specific surface area are the carbonyl group, and as the content of the functional group increases, the carbonyl group spreads to the carboxyl group. The specific surface area of activated carbons increased by 10–68% with an increase in the carbonyl group up to 6% (maximum point of carbonyl group). On the other hand, the specific surface area for WACs increased when the carboxyl group was 10% or below, but decreased by 6–15% when it increased to 10% or excess.

Polyacrylonitrile/pitch nanofibers were prepared by electrospinning as a precursor for a gas sensor material. Pitch nanofibers were properly fabricated by incorporating polyacrylonitrile as an electrospinning supplement component. Polyacrylonitrile/pitch nanofibers were activated with steam at various temperatures followed by subsequent carbonization to make carbon nanofibers with a highly conductive graphitic structure. Steam activation was effective in facilitating gas adsorption onto the carbon nanofibers due to the increased surface area. The carbon nanofibers activated at 800°C had a larger surface area and a lower micro pore fraction resulting in a higher variation in electrical resistance for improved CO gas sensing properties.

OBJECTIVES: Currently, the market for carbon emissions trading has been increasing. In Korea, it is known that traffic mode rate in bike transportation is low. However, if bike transportation system is encouraged and the traffic mode rate is increased, it would be possible to reduce carbon emissions through the trading market. In this study, a practical policy to activate the bike transportation system in Korea will be proposed and verified. METHODS: Past studies regarding bike transportation system in international and domestic metropolitan cities were analyzed. Moreover, detailed reviews on recent carbon emissions trading market were performed. In particular, SWOT analysis on the bike transportation system in Korea and policy topology analysis were conducted. RESULTS: Based on the literature reviews and SWOT analysis, a new bike transportation policy was proposed. Several actual plans to adopt in Korea were proposed. In addition, a new bike transportation policy was analyzed using policy typology model, and a business model related to the cost of implementing the system and CERs were also proposed. CONCLUSIONS : It is concluded that the proposed bike transportation activation policy and several practical plans to connect CERs and a business model including bus, subway, T-money and bike riders to give some incentive were effective and reasonable. It is desired that this study will help Korea to get CERs through bike transportation activation in the future.