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Formed activated carbon (AC) is a multipurpose product with developed adsorption properties that is widely used in various areas of life. To create AC, hard coal has to go through various processes: grinding, granulation, carbonization, physical and/or chemical activation. Presented research was conducted in the professional company manufacturing activated carbons. Studied AC reached the demanded shape of grains thanks to binders added to granulation process. Research on the AC formed using new polymeric binders (applied so far in other branches: pharmacy and construction materials) is presented in this manuscript. Tested binders were not used before to manufacture ACs in the professional technological line. Such polymers as: sodium carboxymethylhydrocellulose (CMHC), poly[1-(2-oxo-1-pyrrolidinyl)ethylene] (POPE) and enriched methyl-hydroxypropyl cellulose MHPC were studied in this work. Conducted research has proven efficiency of 8% CMHC which allowed for proper granulation and carbonization and reached the best parameters. Single- and double-stage activation was investigated for AC with this binder. For newly manufactured AC BET surface and pore volume increased accordingly from 774 m2/g and 0.58 cm3/g (1-stage) to 968 m2/g and 0.72 cm3/g (2-stage). Chemical elemental features of surface of the best AC showed beside elementary carbon also calcium, silicon and aluminum ions as well as groups with an acidic character, phosphates, sulphates and chlorides. The new AC had a higher Mechanical Strength reaching 99.9% and a lower Ash content and Volatile Matter than AC manufactured with previous binder—molasse. The new AC is intended to be directed for full production line and implementation to usage after positive certification. It may be useful in water treatment. It will also find application in the treatment of industrial and municipal wastewater. [ABSTRACT FROM AUTHOR]

Using sodium lignosulfonate as feedstock, ZnCl2 and NaHCO3 co-activated the hierarchical porous carbons (HPCs) were prepared by one-pot pyrolysis with different NaHCO3 dosages (0–4 g) and carbonization temperatures (400–600 °C). Subsequently, phosphotungstate (HPW) was supported with the resulting biochar for the α-pinene hydration reaction to produce α-terpineol. The optimum preparation conditions were determined according to the yield of α-terpineol. The formation mechanism and physicochemical properties of HPCs were analyzed through TG, SEM, XPS, XRD, FT-IR, and N2 adsorption–desorption isotherms. The results demonstrated that NaHCO3 underwent a two-step reaction which liberated a substantial quantity of CO2, thereby enhancing activated carbon's macroporous and mesoporous structures. Simultaneously, NaHCO3 mitigated strong acid gas (HCl) emissions during ZnCl2 activation. Compared with AC450-4:8:0 prepared by ZnCl2 activation alone, the total pore volume of AC450-4:8:2 prepared by co-activation is increased from 0.595 mL/g to 0.754 mL/g and the mesopore rate from 47.7% to 77.8%, which is conducive to reducing the steric hindrance of the hydration reaction and improving the selectivity. Hydration experiments show that the selectivity of α-terpineol is 55.7% under HPW/AC450-4:8:2 catalysis, higher than 31.0% for HPW and 47.4% for HPW/AC450-4:8:0. [ABSTRACT FROM AUTHOR]

Porous carbon materials have been widely used to remove pollutants from the liquid-phase streams. However, their limited pore properties could be a major problem. In this work, the effects of post-washing methods (i.e., water washing and acid washing) on the textural characteristics of the resulting biochar and activated carbon products from pineapple peel biomass were investigated in the carbonization and CO2 activation processes. The experiments were set at an elevated temperature (i.e., 800 °C) holding for 30 min. It was found that the enhancement in pore property reached about a 50% increase rate, increasing from 569.56 m2/g for the crude activated carbon to the maximal BET surface area of 843.09 m2/g for the resulting activated carbon by water washing. The resulting activated carbon materials featured the microporous structures but also were characteristic of the mesoporous solids. By contrast, the enhancement in the increase rate by about 150% was found in the resulting biochar products. However, there seemed to be no significant variations in pore property with post-washing methods. Using the energy dispersive X-ray spectroscopy (EDS) and the Fourier Transform infrared spectroscopy (FTIR) analyses, it showed some oxygen-containing functional groups or complexes, potentially posing the hydrophilic characters on the surface of the resulting carbon materials. [ABSTRACT FROM AUTHOR]

Activated carbon is the preferred adsorbent for gas and water treatment in various industry across the world due to its efficiency, reliability, and accessibility. Recently, in Malaysia, studies are mainly focused on the fabrication of activated carbon from lignocellulosic biomass-based precursors from agricultural waste such as coconut shell, rice husk, and palm kernel shell. Activated carbon fabrication is a two-step process; the precursor will first undergo carbonization, then, activation is carried out either physically or chemically to develop its porous surface for adsorption purposes. The main benefit of activated carbon is the customizable pore structure for different utilization, which can be easily achieved by the chemical activation process. The types and concentration of chemicals used for activation, pre-treatment of precursor, duration of the activation process, and the mass ratio of precursor to chemicals are proven to effectively influence the resulting pore structure. However, the chemicals used in the activation process can be harmful to the environment. Thus, the chemical recovery process is necessary after the activation process. Nonetheless, more in-depth research on producing activated carbon from abundant biomass materials with bio-based chemical agents for activation is needed to achieve an ecological and sustainable manufacturing process. [ABSTRACT FROM AUTHOR]

In the wake of economic and population growth, increased wastewater production poses a challenge related to sewage sludge treatment, which is problematic given its high moisture content, amount, and hazardous characteristics. This study focuses on the hydrothermal carbonization of sewage sludge to produce carbonous material–hydrochar, which may be an alternative to fossil fuels. The effect of process parameters, namely, temperature (180, 240, 300 °C) and duration time (30, 90, 180 min), on hydrochar properties (proximate and ultimate analysis, heating values) and process performance were studied. Obtained results indicate and confirm that hydrothermal carbonization, especially temperature increase, improves the fuel properties of carbonized sewage sludge. The highest low heating value was obtained for hydrochar derived at 300 °C in 180 min (~23 MJ × kg−1). The highest energy gain was noted for hydrochar derived at 240 °C in 180 min (~23%). As well as relatively high mass and energy yield in comparison to other hydrochars, these parameters are considered the most favorable for sewage sludge hydrothermal carbonization. However, high energy consumption (over 1300 kJ × g−1) suggests that more research on the process's economical efficacy is required. [ABSTRACT FROM AUTHOR]

This study presents novel life cycle assessment (LCA) findings on hydrochar production from Saudi-Arabia-based date palm fronds biomass waste using hydrothermal carbonization (HTC). The LCA procedure incorporated normalization, weighting, and improvement assessment. The system boundary encompassed water consumption and energy requirements within a lab setting representing a gate-to-gate process. The OpenLCA 1.11.0 software with the European Life Cycle Database 3.2 (ELCD 3.2) was utilized for the study and we employed the ReCiPe Midpoint (H) 2016 and Environmental Footprint 3.0 (EF 3.0) impact assessment methods. The results indicated that fossil fuel usage represented the most significant impact category with the HTC and drying processes identified as major contributors. It was also observed that the HTC process exerted far greater detrimental impacts on the environment than the biomass grinding process. The overwhelming impact of fossil fuel resources could be mitigated by optimizing the batches of biomass or hydrochar samples in each operation, which could alleviate fossil fuel consumption by up to 94%. The findings emphasize the need for targeted interventions to mitigate the environmental burden and contribute to sustainable hydrochar production. [ABSTRACT FROM AUTHOR]

This study investigates the suitability of different lignocellulosic sources, namely eucalyptus, apple bagasse, and out-of-use wood, for injection into blast furnaces (BFs). While wastes possess carbon potential, their high moisture renders them unsuitable for direct energy utilization. Additionally, the P and K impurities, particularly in apple bagasse, can pose operational and product quality challenges in BF. Thus, different thermochemical processes were performed to convert raw biomass into a more suitable carbon fuel. Low-temperature carbonization was selected for eucalyptus, yielding a biochar with properties closer to the low-rank coal. Hydrothermal carbonization was chosen for apple bagasse and out-of-use wood, resulting in hydrochars with enhanced fuel characteristics and fewer adverse inorganic species but still limiting the amount in binary PCI blends. Thermogravimetry evaluated the cause–effect relationships between coal and coal- and bio-based chars during co-pyrolysis, co-combustion and CO2-gasification. No synergistic effects for char formation were observed, while biochars benefited ignition and reactivity during combustion at the programmed temperature. From heat-flow data in combustion, the high calorific values of the chars were well predicted. The CO2-gasification profiles of in situ chars revealed that lignin-rich hydrochars exhibited higher reactivity and conversion than those with a higher carbohydrate content, making them more suitable for gasification applications. [ABSTRACT FROM AUTHOR]

Exposing catalytically active metal sites in metal–organic frameworks (MOFs) while maintaining porosity is beneficial for increasing electron transport to achieve better electrochemical energy conversion performance. Herein, we propose an in situ method for MOF formation and loading onto TiO2 nanorods (NR) using a simple solution-processable method followed by annealing to obtain TiO2-Co3O4. The as-prepared TiO2-ZIF-67 based photoanodes were annealed at 350, 450, and 550 °C to study the effect of carbonization on photo-electrochemical water oxidation. The successful loading of ZIF-67 on TiO2 and the formation of TiO2-Co3O4 heterojunction were confirmed by XRD, XPS, FE-SEM, and HRTEM analyses. TiO2-Co3O4-450 (the sample annealed at 450 °C) showed an enhanced photocurrent of 2.4 mA/cm2, which was 2.6 times larger than that of pristine TiO2. The improved photocurrent might be ascribed to the prepared p–n heterostructures (Co3O4 and TiO2), which promote electron–hole separation and charge transfer within the system and improve the photoelectrochemical performance. Moreover, the preparation of Co3O4 from the MOF carbonization process improved the electrical conductivity and significantly increased the number of exposed active sites and enhanced the photoresponse performance. The as-prepared ZIF-67 derived TiO2-Co3O4 based photoanodes demonstrate high PEC water oxidation, and the controlled carbonization method paves the way toward the synthesis of low-cost and efficient electrocatalysts. [ABSTRACT FROM AUTHOR]

In this paper, a method for optimizing the mixing ratio of filler coke and binder for high-strength carbon–carbon composites is proposed. Particle size distribution, specific surface area, and true density were analyzed to characterize the filler properties. The optimum binder mixing ratio was experimentally determined based on the filler properties. As the filler particle size was decreased, a higher binder mixing ratio was required to enhance the mechanical strength of the composite. When the d50 particle size of the filler was 62.13 and 27.10 µm, the required binder mixing ratios were 25 and 30 vol.%, respectively. From this result, the interaction index, which quantifies the interaction between the coke and binder during carbonization, was deduced. The interaction index had a higher correlation coefficient with the compressive strength than that of the porosity. Therefore, the interaction index can be used in predicting the mechanical strength of carbon blocks and optimizing their binder mixing ratios. Furthermore, as it is calculated from the carbonization of blocks without additional analysis, the interaction index can be easily used in industrial applications. [ABSTRACT FROM AUTHOR]

The purpose of this study is to improve the oxidation resistance of graphite blocks after graphitization at 2800 °C by introducing a curing process of phenolic resin, used as a binder to control the pore size. Using the methylene index obtained from FTIR, the curing temperature was set to 150 °C, the temperature at which cross-linking most highly occurs. Graphite blocks that had undergone curing, and were carbonized with a slow heating rate, showed increased mechanical and electrical properties. Microstructural observation confirmed that the curing process inhibited the formation of large pores in the graphite block. Therefore, the cured graphite block showed better oxidation resistance in air than a non-cured graphite block. Oxidation of the graphite block was caused by pores created by pyrolysis of the phenolic resin binder, which acted as active sites. [ABSTRACT FROM AUTHOR]

The production of agricultural waste is associated with environmental problems and risks to public health. The general interest demands, as an ecological alternative, the proper management of waste generated by industrial activity through its transformation into value-added products. Carbonization/activation (2 h/2 h) at 700 °C in a vertical furnace (20 K/min), to produce biochar and activated carbon (AC) from bamboo, orange, and paulownia residue, was carried out in a laboratory facility with physical activation by CO2 and steam. The characterization of the carbonaceous material obtained was based on the determination of the N2 adsorption–desorption isotherms at 77 K, the specific surface area with the BET procedure, and its internal structure by means of SEM images. The BET surface area values obtained as a function of the CO2/steam agent used were 911/1182 m2/g, 248/388 m2/g, and 800/1166 m2/g for bamboo, orange, and paulownia, respectively. The range of variation of porosity in paulownia residue generated after steam activation was 485–1166 m2/g, varying depending on the degree of maturity of the biomass used. Research has shown that both the type of activation agent used to produce AC and the degree of plant maturation of the precursor residue affect the quality and characteristics of the final product. [ABSTRACT FROM AUTHOR]

Waste plastics such as polyethylene terephthalate (w-PET) and stockpiled discard coal (d-coal) pose a global environmental threat as they are disposed of in large quantities as solid waste into landfills and are particularly hazardous due to spontaneous combustion of d-coal that produces greenhouse gases (GHG) and the non-biodegradability of w-PET plastic products. This study reports on the development of a composite material, prepared from w-PET and d-coal, with physical and chemical properties similar to that of metallurgical coke. The w-PET/d-coal composite was synthesized via a co-carbonization process at 700 °C under a constant flow of nitrogen gas. Proximate analysis results showed that a carbonized w-PET/d-coal composite could attain up to 35% improvement in fixed carbon content compared to its d-coal counterpart, such that an initial fixed carbon content of 14–75% in carbonized discard coal could be improved to 49–86% in carbonized w-PET/d-coal composites. The results clearly demonstrate the role of d-coal ash on the degree of thermo-catalytic conversion of w-PET to solid carbon, showing that the yield of carbon derived from w-PET (i.e., c-PET) was proportional to the ash content of d-coal. Furthermore, the chemical and physical characterization of the composition and structure of the c-PET/d-coal composite showed evidence of mainly graphitized carbon and a post-carbonization caking ability similar to that of metallurgical coke. The results obtained in this study show potential for the use of waste raw materials, w-PET and d-coal, towards the development of an eco-friendly reductant with comparable chemical and physical properties to metallurgical coke. [ABSTRACT FROM AUTHOR]

The hardened cement paste powder (HCP) powder, devoid of the hydration cementing property, can be regenerated and cemented into a test block with practical strength of almost 60 MPa via CO2 carbonization using appropriate means. This study established a kinetic model of CO2 curing of an HCP powder test block based on the degree of carbonization to study the carbonization reaction kinetic characteristics of the test block. The model was modified according to the characteristics of the evident temperature differences in the reaction kettle in the early, middle, and late stages of the carbonization process. The proposed model can be used to formulate and control the carbonization and cementation processes of HCP powder and can also be applied to describe the kinetics of the reaction processes of other similar systems. [ABSTRACT FROM AUTHOR]

Numerous industries, including footwear, handicrafts, and the automobile industry, utilize leather materials. The main goal of this study was to investigate the effect of input power of the diode laser in laser cutting on vegetable chrome tanned buffalo leather to enhance the cutting process. In the present investigation, carbonization, kerf width, and material removal rate (MRR) were taken as performance measures. The diode-based laser beam machining was designed and fabricated with 2.5 W, 5.5 W, and 20 W diode laser to cut vegetable chrome tanned leather. The high-intensity 20 W diode laser produced lower carbonization, lower kerf width, and higher material removal rate compared with the 2.5 W and 5.5 W diodes. This improved performance was due to the adjustable features associated with this diode laser actuation in the form of circular shape with adjustable diameter. A high power with a lower spot size under pulsed mode can produce higher power density. Since a higher power density can establish less interaction time, it produces lower carbonization. Due to the ability of the 20 W diode laser driver to control the beam shape and size, it could produce a lower kerf width and higher MRR. The optimal parameters for cutting chrome vegetable tanned cow leather were a standoff distance of 18 mm, feed rate of 200 mm/min, and duty cycle of 70%. [ABSTRACT FROM AUTHOR]

Compared with Portland cement, geopolymers have poor carbonization resistance, which will greatly limit the application their application. To improve the carbonization resistance of geopolymers, firstly, the carbonization behavior of the fly ash-metakaolin-based geopolymer was studied through accelerated carbonization tests. Secondly, different amounts of Ca(OH)2 were introduced into the composite system, and the modification effect of the carbonization resistance of the modified geopolymer was studied. Finally, the modification effect of Ca(OH)2 on the fly ash-metakaolin-based geopolymers was analyzed, and the modification mechanism was explored. It was found that adding Ca(OH)2 to the fly ash-metakaolin-based geopolymer could significantly improve its initial compressive strength, but its strength after carbonization remained basically unchanged; meanwhile, the compressive strength of the terpolymer after carbonization clearly decreased after adding Ca(OH)2. Compared with ordinary Portland cement, the carbonization rate of fly ash-metakaolin-based geopolymer is faster, and the addition of Ca(OH)2 can inhibit the development of its carbonization depth. With increased carbonization age, the alkalinity of the geopolymer decreased, and the addition of Ca(OH)2 inhibited the decrease in the alkalinity of the geopolymer. The addition of Ca(OH)2 improved the microstructure of the geopolymers, the pore structure became denser, and the pore size became smaller size after carbonization. The hydration products of fly ash-metakaolin-based geopolymer are mainly amorphous silicaluminate gel and C–S–H gel, and Ca(OH)2 forms in the hydration products of terpolymer with the incorporation of Ca(OH)2, which is conducive to improving the carbonization resistance. In summary, Ca(OH)2 can play a good role in modifying the carbonization resistance of fly ash-metakaolin-based geopolymers. [ABSTRACT FROM AUTHOR]

The double-sided carbonization of poplar with different sections forms a three-layer structure inspired by tree water transpiration. A photothermal evaporation comparison experiment was conducted to simulate the influence of solar radiation intensity (1 kW·m−2) on uncarbonized and single- and double-sided carbonized poplar specimens. The tissue structure, chemical functional group changes, and profile density of the specimens were analyzed using scanning electron microscopy, Fourier transform infrared spectrometry, and X-ray profile density testing, respectively. The results showed that the tissue structure of the specimen changed after treatment, and the relationship of water evaporation was shown as follows: cross-section (C) > Radial section (R) > Tangential section (T), and Double-sided carbonized poplar (DCP) > Single-sided carbonized poplar (SCP) > Non-carbonized poplar (NCP). Of these, the maximum photothermal evaporation was from the cross-section of the double-sided carbonized poplar (NCPC) with a value of 1.32 kg·m−2·h−1, which was 21.97% higher than single-sided carbonized poplar (SCPC) and 37.88% higher than non-carbonized poplar (NCPC). Based on the results, double-sided carbonization three-layer structure treatment can improve the evaporation force of the poplar interface, thereby improving the moisture migration ability of wood, and can be applied to solar interface absorber materials. [ABSTRACT FROM AUTHOR]

With the special porous structure and super-long carbon sequestration characteristic, the biochar has shown to have potential in improving soil fertility, reducing carbon emissions and increasing soil carbon sequestration. However, the biochar technology has not been applied on a large scale, due to the complex structure, long transportation distance of raw materials, and high cost. To overcome these issues, the brazier-type gasification and carbonization furnace is designed to carry out dry distillation, anaerobic carbonization and have a high carbonization rate under high-temperature conditions. To improve the operation and maintenance efficiency, we formulate the operation of the brazier-type gasification and carbonization furnace as a dynamic multi-objective optimization problem (DMOP). Firstly, we analyze the dynamic factors in the work process of the brazier-type gasification and carbonization furnace, such as the equipment capacity, the operating conditions, and the biomass treated by the furnace. Afterward, we select the biochar yield and carbon monoxide emission as the dynamic objectives and model the DMOP. Finally, we apply three dynamic multiobjective evolutionary algorithms to solve the optimization problem so as to verify the effectiveness of the dynamic optimization approach in the gasification and carbonization furnace. [ABSTRACT FROM AUTHOR]

Composites of carbons with metal oxides and metal sulfides have attracted a lot of interest as materials for energy conversion and storage applications. Herein, we report on novel N,O-doped carbon/ZnO/ZnS and N,O-doped carbon/ZnO composites (generally named C-(MOF-5/PANI)), synthesized by the carbonization of metal–organic framework MOF-5/polyaniline (PANI) composites. The produced C-(MOF-5/PANI)s are comprehensively characterized in terms of composition, molecular and crystalline structure, morphology, electrical conductivity, surface area, and electrochemical behavior. The composition and properties of C-(MOF-5/PANI) composites are dictated by the composition of MOF-5/PANI precursors and the form of PANI (conducting emeraldine salt (ES) or nonconducting emeraldine base). The ZnS phase is formed only with the PANI-ES form due to S-containing counter-ions. XRPD revealed that ZnO and ZnS existed as pure wurtzite crystalline phases. PANI and MOF-5 acted synergistically to produce C-(MOF-5/PANI)s with high SBET (up to 609 m2 g−1), electrical conductivity (up to 0.24 S cm−1), and specific capacitance, Cspec, (up to 238.2 F g−1 at 10 mV s−1). Values of Cspec commensurated with N content in C-(MOF-5/PANI) composites (1–10 wt.%) and overcame Cspec of carbonized individual components PANI and MOF-5. By acid etching treatment of C-(MOF-5/PANI), SBET and Cspec increased to 1148 m2 g−1 and 341 F g−1, respectively. The developed composites represent promising electrode materials for supercapacitors. [ABSTRACT FROM AUTHOR]

Oil leakage incidentally occurs and leads to environmental disasters. Because of their porous and hydrophobic characteristics, graphene sponges are often studied as an oil adsorbent to repair oil spills at sea. Graphene materials are very expensive, and their biological toxicity has been given serious concerns; however, the easier preparation and eco-friendly, biomass-derived porous carbon materials can be used as an alternative to graphene materials. In this study, we prepared a porous carbon sponge (PCS) for oil and organic solvent removal by carbonizing white-rot fungus Phanerochaete chrysosporium, a fast-growing microorganism for the production of lignin-degrading enzymes and the environmental remediation. P. chrysosporium fungus balls were converted into black PCS by carbonization at high temperatures, where PCS was light (density of 56 g/L), hydrophobic (contact angle of 115°) and porous. According to the results of BET and XPS analysis, the surface area of PCS was 14.43 m2/g, and the carbon in PCS is mainly sp2 carbon. PCS could adsorb pure oils and organic solvents within seconds. The adsorption capacities of PCS were 20.7 g/g for gasoline, 30.1 g/g for peanut oil, 27.7 g/g for toluene, 18.5 g/g for dodecane, 32.5 g/g for chloroform, 27.1 g/g for tetrahydrofuran, 23.7 g/g for acetone and 13.7 g/g for ethanol. According to the reusability study, there was no obvious capacity loss after recycling up to 10 cycles. Our results indicated that white-rot fungi could be adopted as a cheap carbon resource for oil and organic solvent removal. [ABSTRACT FROM AUTHOR]

Volatile organic compounds (VOCs) released in air represent a major potential for environmental pollution. Capture methods based on activated biochar have attracted attention because of their low cost and for the high removal capacity of the material due to its physical and chemical properties. In this paper, activated biochars were developed and their adsorption performance for VOC capture was evaluated. In the first step, biochars derived from rapeseed cake (RSC) and walnut shells (WSC) were obtained through a carbonization process and then were activated using basic/acid agents (KOH/H2SO4) to increase their performance as adsorbents. Acetone and toluene were used as the VOC templates. The adsorption capacities of toluene and acetone for non-activated biochars were reduced (26.65 mg/g), while that of activated biochars increased quite significantly, up to 166.72 mg/g, and the biochars activated with H2SO4 presented a higher adsorption capacity of VOCs than the biochars activated with KOH. The higher adsorption capacity of biochars activated with H2SO4 can be attributed to their large surface area, and also to their larger pore volume. This activated biochar adsorbent could be used with good results to equip air purification filters to capture and remove VOCs. [ABSTRACT FROM AUTHOR]

The leather materials are used in a multitude of sectors, including footwear, apparel, handicrafts, and the automotive industry. Due to the radiant heat generated by a laser beam, the laser cutting of leather results in a carbonized cut edge. There is currently no technology available for measuring the carbonization along the contour edges of leather. The purpose of this experimental investigation was to determine the impact of power diode-based laser cutting on the carbonization of machined buffalo leather with the help of a digital microscope to improve the machining process. The ATR-FTIR spectrum was used to analyze the carbon-related functional group in the mid-IR spectrum of carbonized leather samples. It was found that the proposed method can measure the amount of carbon deposition in the cutting zone. The lower amplitude duty cycle with higher feed rate can reduce carbon formation owing to the lower thermal energy distribution. The amplitude (4.5 V), duty cycle (70%) and feed rate (90 mm/s) can produce optimal performance measures. [ABSTRACT FROM AUTHOR]

Pomelo peel (PP) is a kind of solid waste that is produced in the processing industry of honey pomelo. This study deeply explored the feasibility of recycling PP in the form of hydrochar (HC) by microwave-assisted hydrothermal carbonization (HTC) technology. Under the non-catalytic reaction conditions, the yield of hydrochar initially increased with the rise of reaction temperature (150–210 °C) until it remained relatively stable after 210 °C. Under the CaO-catalytical reaction condition, the yield of hydrochar did not change much at first (150–190 °C) but decreased significantly when the reaction temperature exceeded 190 °C. After the microwave-assisted HTC treatment, the PP-derived HC presented higher aromaticity, carbonization degree, porosity, and caloric value. Compared with raw PP, the nutrients in HC were more stable (conducive to being used as slow-release fertilizer). The application of CaO increased the pH value of HC and effectively promoted the accumulation of phosphorus in HC. The HC produced at 210 °C without any catalyst possessing a high devolatilization ability. Additionally, the HC obtained at 190 °C with CaO as the catalyst presented a high combustion property. In general, PP-derived HC showed great application potential in the field of soil remediation/improvement and solid fuels. This preliminary study would undoubtedly provide some important fundamental understanding of the microwave-assisted HTC of PP. [ABSTRACT FROM AUTHOR]

The influence of three coal tar pitches (CTPs), having softening points at 86, 94, and 103 °C, on the thermal behaviour of a defrosted high-volatile coal during co-carbonization and co-pyrolysis was studied. The following research techniques were used: X-raying of the coked charge, TG/FT-IR, ATR and UV spectroscopies, extraction, SEM, STEM, and XRD. It was determined that CTP additives change the structure of the coal plastic layer, the thickness of its zones, and the ordering degree of the structure of semi-cokes to a different extent and independently from their softening points. The softening points of CTPs do not influence the composition and yield of volatile products emitted from blends with pitch as well as the composition, structural-chemical parameters, and topological structure of material extracted from coal blends. It is suggested that such a lack of existence of any correlation between the softening points of CTPs and the degree of their influence on the thermal behaviour of coal was caused by the presence of the atoms of metals (Fe and Zn) in the CTPs. These atoms change the course of the carbonization of the CTPs themselves and their influence on organic substance of coal in blends with CTPs. [ABSTRACT FROM AUTHOR]

Nowadays, the use of biomass to produce cathode materials for lithium–sulfur (Li-S) batteries is an excellent alternative due to its numerous advantages. Generally, biomass-derived materials are abundant, and their production processes are environmentally friendly, inexpensive, safe, and easily scalable. Herein, a novel biomass-derived material was used as the cathode material in Li-S batteries. The synthesis of the new carbonaceous materials by simple carbonization and washing of water kefir grains, i.e., a mixed culture of micro-organisms, is reported. The carbonaceous materials were characterized morphologically, texturally and chemically by using scanning electron microscopy, N2 adsorption–desorption, thermogravimetric analysis, X-ray diffraction, and both Raman and X-ray photoelectron spectroscopy. After sulfur infiltration using the melt diffusion method, a high sulfur content of ~70% was achieved. Results demonstrated that the cell fitted with a cathode prepared following a washing step with distilled water after carbonization of the water kefir grains only, i.e., not subjected to any chemical activation, achieved good electrochemical performance at 0.1 C. The cell reached capacity values of 1019 and 500 mAh g−1 sulfur for the first cycle and after 200 cycles, respectively, at a high mass loading of 2.5 mgS cm−2. Finally, a mass loading study was carried out. [ABSTRACT FROM AUTHOR]

Pore structure and composition of cement paste are the main two factors in controlling the sulfate attack on concrete, but the influence of carbonization on pore structure and composition is often ignored in sulfate attack. Therefore, will the damage performance of concrete partially exposed to sulfate solution be different avoiding the alterations of pore structure and composition due to carbonation? In this paper, the cement pastes were partially immersed in 5 wt. % sodium sulfate solution, with N2 as protective gas to avoid carbonation (20 ± 1°C, RH 65 ± 5%). Pore structures of cements were changed by introducing different contents of limestone powders (0 wt. %, 10 wt. %, 20 wt. %, and 30 wt. %) into cement pastes. The damage performance of the specimens was studied by 1H NMR, XRD and SEM. The results showed that the immersion zone of pure cement paste under N2 atmosphere remained intact while serious damage occurred in the evaporation zone. However, the damage of cement + limestone powders pastes appeared in the immersion zone rather than in the evaporation zone and cement pastes containing more limestone were more severely damaged. Compositional analysis suggested that the damage of the evaporation zone or the immersion zone was solely caused by chemical attack where substantial amount of gypsums and ettringites were filled in the pore volumes. Introduction of limestone powders led to the increase of the pore sizes and porosity of cement pastes, causing the damage occurred in the immersion zone not in the evaporation zone. [ABSTRACT FROM AUTHOR]

This paper characterizes the carbonization process in terms of the utilization of distillery waste in a laboratory-scale reactor. Due to the increase in market prices of wood and environmental protection laws, biomass waste, including distillery waste, is a potential source for biochar production. An experimental investigation of the carbonization process was carried out for different mixtures of distillery waste and oak sawdust. The obtained results showed that due to the European Standard, biochar from distillery waste could be used for the production of charcoal briquettes for barbecue applications. In addition, biochar from carbonization samples with 66, 50, and 33% distillery waste meet the standards defined by the International Biochar Initiative for HMs content. The analysis of the dynamics of the heating rate showed that adding wood to distillery waste significantly shortens the carbonization process, but this reduces the number of bio-oils produced and its calorific value. [ABSTRACT FROM AUTHOR]

Copper nanoparticle (Cu NP) is a promising replacement for noble metal nanoparticles due to its high electrical conductivity and low cost. However, Cu NPs are relatively active compared to noble metals, and current ways of protecting Cu NPs from oxidation by encapsulation have severe drawbacks, such as a long reaction time and complicated processes. Here, a facial and effective method to prepare the mesosphere of carbon-shelled copper nanoparticles (Cu@MC) was demonstrated, and the resulting Cu@MC was both highly electrically conductive and thermally stable. Cu@organic (100 nm) was first synthesized by the reduction of Cu ions with poly (vinyl pyrrolidone) (PVP) and sodium poly ((naphthalene-formaldehyde) sulfonate) (Na-PNFS) as soft templates. Then, the carbon shells were obtained by in situ carbonization of the polymer soft templates. The Cu@organic and Cu@MC showed an anti-oxidation ability up to 175 and 250 °C in the air atmosphere, respectively. Furthermore, the Cu@MC exhibited excellent volume resistivity of 7.2 × 10−3 Ω·cm under 20 MPa, and showed promising application potential in electric sensors and devices. [ABSTRACT FROM AUTHOR]

Heteroatom-doped conductive carbon nanomaterials are promising for energy and catalysis applications, but there are few reports on increasing their heteroatom doping content and conductivity simultaneously. In this manuscript, we use 2-(4-aminophenyl)-5-aminobenzimidazole as the diamine monomer to prepare polyamic acid with asymmetric structural units doped with phosphoric acid (PA) and polyacrylonitrile (PAN) as innovative composite precursors, which are then electrospun into nanofiber films. After stabilization and carbonization, the electrospun fibers are converted into N/P co-doped electrospun carbon nanofiber films (ECNFs) with high heteroatom content, including 4.33% N and 0.98% P. The morphology, structure, and conductivity of ECNFs were systematically characterized. The ECNFs doped with 15 wt.% PA exhibited conductivity that was 47.3% higher than that of the ECNFs undoped with PA, but the BET surface area decreased by 23%. The doped PA in the precursor nanofibers participated in the cyclization of PAN during thermal stabilization, as indicated by infrared spectroscopy and thermogravimetric analysis results. X-ray diffraction and Raman results indicate that a moderate amount of PA doping facilitated the formation of ordered graphitic crystallite structures during carbonization and improved the conductivity of ECNFs. [ABSTRACT FROM AUTHOR]

This publication presents a series of data of one of the most difficult chemical processes to implement in industrial conditions. Obtaining soda using the Solvay technique is a process with a world volume of about 28 Tg per year. The process is extremely physico-chemically complex and environmentally burdensome. The paper presents information on a multi-component system containing three phases with a chemical reaction. Calculations for such systems and their engineering are very complicated, but the authors show how the results of this work can be applied. This paper also describes modifications of the soda process to minimize the environmental burden and minimize the production input of Na2CO3. The modifications were beneficial in reducing CO2 emissions and increased the efficiency of the soda process, resulting in a measurable financial benefit. At the scale of the plant where the experiment was carried out, this reduction in CO2 emissions amounts to 7.93 Gg per year. [ABSTRACT FROM AUTHOR]

Geopolymers have attracted extensive attention in the marine environment because of its special reticulate nanostructure. Gel evolutions of copper tailing-based green geopolymers were studied under air, deionized water, seawater, freeze–thaw cycle and carbonization environments. Their mechanical properties and microstructures were characterized by compressive strength measurement, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR) and scanning electron microscopy (SEM). It was found that the deionized water and natural marine water exposure promoted the evolution degree of geopolymers and improved their compressive strength, while exposure to the carbonization environment weakened the gel evolution and decreased the cross-linking degree of the Sodium aluminosilicate hydrate (N-A-S-H)gel structure, resulting in a decline of compressive strength. The geopolymer exposed in the freeze–thaw cycle exhibited the worst deterioration due to the expansion caused by the crystallization in the geopolymer. These results are essential and beneficial to further understanding the gel formation process in various marine environments and could promote the investigation of green concrete. [ABSTRACT FROM AUTHOR]

The article is devoted to the study of the influence of residual sulfuric and phosphoric acids on the process of processing large-tonnage phosphogypsum (PG) waste into calcium carbonate. In the Russian Federation, about 10 percent of existing phosphogypsum waste is processed into construction materials. Acidic impurities (phosphoric and sulfuric acids) in their composition are an obstacle to the use of phosphogypsum for the production of binders. This study finds that impurities also reduce the chemical activity of phosphogypsum. At the same time, the paper focuses on the potential of phosphogypsum for the production of calcium carbonate. This article investigated the amount of impurities in phosphogypsum. The results show that during automatic washing of phosphogypsum, losses are approximately 30–35 wt. %. It was also found that phosphogypsum by 22% consists of impurities of phosphoric and sulfuric acid. These acids are characteristic waste products of extraction phosphoric acid (EPA) production. By ASTM C471M-20ae1, the content of calcium sulfate dehydrate and hemihydrate before and after washing was determined. A thermodynamic calculation of the proposed interaction of phosphogypsum with carbonates showed that the characteristic reaction is possible. The conversion process of phosphogypsum to get the corresponding calcium carbonate was carried out at 70 °C. Data on the chemical composition of the reaction products, obtained by X-ray fluorescence analysis on a Shimadzu EDX-7000 spectrometer, showed that some reactions proceed incompletely and need the selection of optimal conditions. The potential commercial benefits of processing phosphogypsum by carbonization were defined for products such as calcium carbonate or its derivatives. [ABSTRACT FROM AUTHOR]

A relevant issue with charred exteriors is the inconsistency of the result, which makes service life predictions complicated. Contact charring enables the creation of a very evenly modified surface with accurate control of temperature and modification time, but the weathering properties are questionable. This paper evaluated the effect of the modification time relative to char layer and transition zone thickness, wood species and material density in an artificial weathering test. The results revealed higher color stability in connection to longer modification time, but also an increase in the cracked surface area. Cracking was heavily dependent on the modification regime and increased with increasing char and transition zone thicknesses. Dense spruce had the highest color stability with the most severe modification regime, but char layer thickness varied more than on other wood types. Furthermore, species-dependent cracking patterns affected the final result as the small-scale flaking experienced by birch increased the washing off of char. It is likely an even higher modification temperature with a shorter modification time is needed to produce sufficient weathering resistance suitable for exterior uses. [ABSTRACT FROM AUTHOR]

The preparation of nitrogen-containing porous carbon (NCPC) materials by controlled carbonization is an exciting topic due to their high surface area and good conductivity for use in the fields of electrochemical energy storage and conversion. However, the poor controllability of amorphous porous carbon prepared by carbonization has always been a tough problem due to the unclear carbonation mechanism, which thus makes it hard to reveal the microstructure–performance relationship. To address this, here, we comprehensively employed reactive molecular dynamics (ReaxFF-MD) simulations and first-principles calculations, together with machine learning technologies, to clarify the carbonation process of polypyrrole, including the deprotonation and formation of pore structures with temperature, as well as the relationship between microstructure, conductance, and pore size. This work constructed ring expressions for PPy thermal conversion at the atomic level. It revealed the structural factors that determine the conductivity and pore size of carbonized products. More significantly, physically interpretable machine learning models were determined to quantitatively express structure factors and performance structure–activity relationships. Our study also confirmed that deprotonation preferentially occurred by desorbing the dihydrogen atom on nitrogen atoms during the carbonization of PPy. This theoretical work clearly reproduces the microstructure evolution of polypyrrole on an atomic scale that is hard to do via experimentation, thus paving a new way to the design and development of nitrogen-containing porous carbon materials with controllable morphology and performance. [ABSTRACT FROM AUTHOR]

For the first time, a comprehensive review of the literature data on the use of apricot (Prunus armeniaca) biomass components as a sorption material for the treatment of wastewater and environmental water from various pollutants is carried out in the present study. In addition to a comprehensive analysis of contemporary studies, the current work carried out its own microstructural and energy dispersive studies. It shows that apricot kernel shell is a promising raw material for obtaining sorption materials that can be used to extract various pollutants from aqueous media. The parameters of sorption interaction are presented, at which the highest rate of removal of pollutants was achieved. It is shown that the sorption capacity of apricot biomass components can be increased by modifying it with various chemical reagents, as well as other physical and physicochemical methods. We reveal that most publications consider the use of the latter as a raw material for the production of activated carbons. It is established that the surface area and total pore space of activated carbons from apricot kernel shells depend on the modes of carbonization and activation. It is shown that activated carbons are effective adsorbents for removing various pollutants (metal ions, dyes, oil and oil products) from aqueous media. It was found that the adsorption isotherms of pollutants in most cases are best described by the Langmuir and Freundlich models, and the process kinetics is most often described by the pseudo-second-order model. The possibility of improving the sorption characteristics of apricot biomass during chemical or physicochemical treatment is also shown. [ABSTRACT FROM AUTHOR]

The main aim of the study was to synthesize and analyze spectral data to determine the structure and stereometry of the carbon-based porous material internal structure. Samples of a porous biomaterial were synthesized through anionic polymerization following our own patent and then carbonized. The samples were investigated using MALDI ToF MS, FTIR ATR spectroscopy, optic microscopy, SEM, confocal laser scanning microscopy and CMT imaging. The analysis revealed the chemical and stereological structure of the obtained porous biomaterial. Then, the parameters characterizing the pore geometry and the porosity of the samples were calculated. The developed material can be used to collect adsorption of breathing phase samples to determine the parity composition of exhaled air. [ABSTRACT FROM AUTHOR]

In the present study, graphite blocks were fabricated using synthetic graphite scrap and phenolic resin, and the effect of the heating rate during carbonization on their mechanical and electrical characteristics was examined. While varying the heating rate from 1, 3, 5, and 7 to 9 °C/min, the microstructure, density, porosity, flexural strength, compressive strength, and electrical resistivity of the fabricated graphite blocks were measured. As the heating rate increased, the pores in the graphite blocks increased in size, and the shape of the gas release paths became more irregular. Overall, it was found that increases in the heating rate led to the degradation of the graphite blocks' mechanical and electrical properties. [ABSTRACT FROM AUTHOR]

Nowadays one of the biggest challenges for carbon materials is their use in CO2 capture and their use as electrocatalysts in the oxygen reduction reaction (ORR). In both cases, it is necessary to dope the carbon with nitrogen species. Conventional methods to prepare nitrogen doped carbons such as melamine carbonization or NH3 treatment generate nitrogen doped carbons with insufficient nitrogen content. In the present research, a series of activated carbons derived from MOFs (ZIF-8, ZIF-67) are presented. Activated carbons have been prepared in a single step, by pyrolysis of the MOF in an inert atmosphere, between 600 and 1000 °C. The carbons have a nitrogen content up to 20 at.% and a surface area up to 1000 m2/g. The presence of this nitrogen as pyridine or pyrrolic groups, and as quaternary nitrogen are responsible for the great adsorption capacity of CO2, especially the first two. The presence of Zn and Co generates very different carbonaceous structures. Zn generates a greater porosity development, which makes the doped carbons ideal for CO2 capture. Co generates more graphitized doped carbons, which make them suitable for their use in electrochemistry. [ABSTRACT FROM AUTHOR]

This correction notice states that Feng Qian has requested the removal of his name from the author list of a publication. The authorship list has been amended to reflect this change, and the contributions of the remaining authors have been updated. All authors, including Feng Qian, agreed to this change, and it has been approved by the Academic Editor. The scientific conclusions of the publication are unaffected. [Extracted from the article]

The disposal of agricultural wastes such as fresh banana peels (BPs) is an environmental issue. In this work, fresh BPs were successfully transformed into nitrogen-doped carbon nanoparticles (N-CNPs) by using a high shear mixer facilitated crushing method (HSM-FCM) followed by carbonization under Ar atmosphere. Ammonia-activated N-CNPs (N-CNPs-NH3) were prepared via subsequent ammonia activation treatments at a high temperature. The as-prepared N-CNPs and N-CNPs-NH3 materials both exhibited high surface areas (above 700 m²/g) and mean particle size of 50 nm. N-CNPs-NH3 showed a relatively higher content of pyridinic and graphitic N compared to N-CNPs. In alkaline media, N-CNPs-NH3 showed superior performances as an oxygen reduction reaction (ORR) catalyst (E0 = -0.033 V, J = 2.4 mA/cm²) compared to N-CNPs (E0 = 0.07 V, J = 1.8 mA/cm²). In addition, N-CNPs-NH3 showed greater oxygen reduction stability and superior methanol crossover avoidance than a conventional Pt/C catalyst. This study provides a novel, simple, and scalable approach to valorize biomass wastes by synthesizing highly efficient electrochemical ORR catalysts. [ABSTRACT FROM AUTHOR]

Four porous carbon samples denoted as LSC-1, LSC-2, LCS-3, and LSC-4 were prepared by carbonization of loofah sponge pretreated by ZnCl2 activation, immersion in N,N-dimethylformamide (DMF), DMF-assisted solvothermal and melamine-assisted hydrothermal processes, and the specific surface areas were 1007, 799, 773, and 538 m2.g-1 with mainly micropores, respectively. Electrocapacitive properties of four porous carbon-based electrodes were investigated with cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy in symmetric supercapacitors. All the cyclic voltammetries of four types of supercapacitors showed a rectangular shape, even under a high scan rate of 500 mV.s-1. The capacitances of LSC-1, LSC-2, LSC-3, and LSC-4 were 107.4, 92.5, 60.3, and 82.3 F.g-1 at the current density of 0.1 A.g-1, respectively, and LSC-1 displayed the excellent capacitance retention of about 81.3% with a current density up to 5 A.g-1. All supercapacitors showed excellent electrochemical stability, and the LSC-1-based supercapacitor showed a cycle stability with 92.6% capacitance retention after 5000 cycles at 1 A.g-1. The structure-property relationship of LSC samples is discussed and analyzed on the basis of the experimental data. [ABSTRACT FROM AUTHOR]

A carbon solid acid with large surface area (CSALA) was prepared by partial carbonization of H3PO4 pre-treated peanut shells followed by sulfonation with concentrated H2SO4. The structure and acidity of CSALA were characterized by N2 adsorption--desorption, scanning electron microscopy (SEM), X-ray powder diffraction (XRD), 13C cross polarization (CP)/magic angle spinning (MAS) nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), Fourier transform-infrared spectroscopy (FT-IR), titration, and elemental analysis. The results demonstrated that the CSALA was an amorphous carbon material with a surface area of 387.4 m²/g. SO3H groups formed on the surface with a density of 0.46 mmol/g, with 1.11 mmol/g of COOH and 0.39 mmol/g of phenolic OH. Densities of the latter two groups were notably greater than those observed on a carbon solid acid (CSA) with a surface area of 10.1 m²/g. The CSALA catalyst showed better performance than the CSA for the hydrolysis of cyclohexyl acetate to cyclohexanol. Under optimal reaction conditions, cyclohexyl acetate conversion was 86.6% with 97.3% selectivity for cyclohexanol, while the results were 25.0% and 99.4%, respectively, catalyzed by CSA. The high activity of the CSALA could be attributed to its high density of COOH and large surface area. Moreover, the CSALA showed good reusability. Its catalytic activity decreased slightly during the first two cycles due to the leaching of polycyclic aromatic hydrocarbon-containing SO3H groups, and then remained constant during following uses. [ABSTRACT FROM AUTHOR]

Soda lignin does not have thermal flowing characteristics and it is impossible for it to be further thermally molded. To achieve the fusibility of soda lignin for fiber preparation by melt-spinning, an effective method for soda lignin modification was conducted by cooking it with polyethylene glycol (PEG) 400 at various ratios. The higher the ratio of PEG that was used, the more PEG molecular chains were grafted at the alpha carbon of the soda lignin through ether bonds, resulting in lower thermal transition temperatures and more excellent fusibility. The modified soda lignin with a weight ratio of lignin to PEG of 1:4 exhibited a relative thermal stability of molten viscosity at selected temperatures. Thereafter, the resultant fusible soda lignin was successfully melt-spun into filaments with an average diameter of 33 ± 5 µm, which is smaller than that of some industrial lignins. Accordingly, it is possible to utilize soda lignin to produce fibrous carbonaceous materials. [ABSTRACT FROM AUTHOR]

Woodceramics were fabricated in a vacuum through carbonization of wood powder impregnated with phenol formaldehyde (PF) resin. The effects of carbonization temperature and mass ratio of wood/resin on electromagnetic interference (EMI) shielding effectiveness (SE) and morphology of woodceramics were explored. The PF resin made wood cell walls have the characteristics of glassy carbon. Wood axial tracheid and ray cells were filled with more glassy carbon by increasing addition of PF resin. Moreover, the increase of carbonization temperature was beneficial to improving SE. Woodceramics (mass ratio 1:1) obtained at 1000 °C presented a medium SE level between 30 MHz and 1.5 GHz. [ABSTRACT FROM AUTHOR]

Long cycle performance is a crucial requirement in energy storage devices. Newformulations and/or improvement of "conventional" materials have been investigated in order to achieve this target. Here we explore the performance of a novel type of carbon nanospheres (CNSs) with three heteroatom co-doped (nitrogen, phosphorous and sulfur) and high specific surface area as anode materials for lithium ion batteries. The CNSs were obtained from carbonization of highly-crosslinked organo (phosphazene) nanospheres (OPZs) of 300 nm diameter. The OPZs were synthesized via a single and facile step of polycondensation reaction between hexachlorocyclotriphosphazene (HCCP) and 4,41-sulphonyldiphenol (BPS). The X-ray Photoelectron Spectroscopy (XPS) analysis showed a high heteroatom-doping content in the structure of CNSs while the textural evaluation from the N2 sorption isotherms revealed the presence of micro- and mesopores and a high specific surface area of 875 m2/g. The CNSs anode showed remarkable stability and coulombic efficiency in a long charge-discharge cycling up to 1000 cycles at 1C rate, delivering about 130 mA·h·g-1. This study represents a step toward smart engineering of inexpensive materials with practical applications for energy devices. [ABSTRACT FROM AUTHOR]

This paper presents an idea of using carbonized electrospun Polyacrylonitrile (PAN) fibers as a sensor material in a structural health monitoring (SHM) system. The electrospun PAN fibers are lightweight, less costly and do not interfere with the functioning of infrastructure. This study deals with the fabrication of PAN-based nanofibers via electrospinning followed by stabilization and carbonization in order to remove all non-carbonaceous material and ensure pure carbon fibers as the resulting material. Electrochemical impedance spectroscopy was used to determine the ionic conductivity of PAN fibers. The X-ray diffraction study showed that the repeated peaks near 42° on the activated nanofiber film were a and β phases, respectively, with crystalline forms. Contact angle, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR) were also employed to examine the surface, thermal and chemical properties of the carbonized electrospun PAN fibers. The test results indicated that the carbonized PAN nanofibers have superior physical properties, which may be useful for structural health monitoring (SHM) applications in different industries. [ABSTRACT FROM AUTHOR]

Three isostructural metal-organic frameworks, (MOFs), [Fe(OH)(1,4-NDC)] (1), [Al(OH)(1,4-NDC)] (2), and [In(OH)(1,4-NDC)] (3) have been synthesized hydrothermally by using 1,4-naphthalene dicarboxylate (1,4-NDC) as a linker. The MOFs were characterized using various techniques and further used as precursor materials for the synthesis of metal/metal oxide nanoparticles inserted in a carbon matrix through a simple thermal conversion method. The newly synthesized carbon materials were characterized by scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy analysis, powder X-ray diffraction and BET analysis. The results showed that the MOF-derived carbon composite materials maintained the morphology of the original MOF upon carbonization, and confirmed the insertion of metal/metal oxide particles in the carbon matrix. [ABSTRACT FROM AUTHOR]

Nitrogen- and micropore-containing carbon nanotubes (NMCNTs) were prepared by carbonization of nitrogen-enriched, polymer-coated carbon nanotubes (CNTs), and the electrochemical performances of the NMCNTs with different heteroatom contents were investigated. NMCNTs-700 containing 9.1 wt% nitrogen atoms had a capacitance of 190.8 F/g, which was much higher than that of pristine CNTs (48.4 F/g), despite the similar surface area of the two CNTs, and was also higher than that of activated CNTs (151.7 F/g) with a surface area of 778 m2/g and a nitrogen atom content of 1.2 wt%. These results showed that pseudocapacitive effects play an important role in the electrochemical performance of supercapacitor electrodes. [ABSTRACT FROM AUTHOR]

A large amount of biomass straw waste is generated every year in the world, which can cause serious environmental pollution and resource waste if disposed of improperly. At present, biomass-derived porous carbon materials prepared from biomass waste as a carbon source have garnered attention due to their renewability, huge reserves, low cost, and environmental benevolence. In this work, high-performance carbon materials were prepared via a one-step carbonization-activation method and ball milling, with waste tobacco straw as precursor and nano-ZnO as template and activator. The specific surface area and porous structure of biomass-derived carbon could be controlled by carbonization temperature, which is closely related to the electrochemical performances of the carbon material. It was found that, when the carbonization temperature was 800 °C, the biochar possesses maximum specific surface area (1293.2 m2·g−1) and exhibits high capacitance of 220.7 F·g−1, at 1 A·g−1 current density in a three-electrode configuration with 6 M KOH aqueous solution. The capacitance retention maintained about 94.83% at 5 A·g−1 after 3000 cycles. This work proves the porous biochar derived from tobacco straws has a great potential prospect in the field of supercapacitors. [ABSTRACT FROM AUTHOR]

Lightweight carbon foams with excellent electromagnetic interference (EMI) shielding performance were prepared by carbonization process, using isocyanate-based polyimide foams as carbon precursors. The influence of carbonization temperature and graphene-doping on the morphological, electrical and EMI shielding effectiveness (SE) of corresponding carbon foams was studied in detail. Results showed that the addition of graphene was beneficial to the improvement of electrical conductivity and EMI shielding performance of carbon foams. The electrical conductivity of carbon foams increased with the carbonization temperature which was related to the increase of graphitization degree. Collapse of foam cells was observed at higher carbonization temperatures, which was detrimental to the overall EMI SE. The optimal carbonization temperature was found at 1100 °C and the carbon foams obtained from 0.5 wt% graphene-doped foams exhibited a specific EMI SE of 2886 dB/(g/cm3), which shows potential applications in fields such as aerospace, aeronautics and electronics. [ABSTRACT FROM AUTHOR]

The augmented demands of textile materials over time have brought challenges in the disposal of substantial volumes of waste generated during the processing and end of life of such materials. Taking into consideration environmental safety due to discarding of textile waste, it becomes critical to recuperate useful products from such waste for economic reasons. The present work deals with the preparation of porous and electrically conductive activated carbon fabric by a novel single stage method of simultaneous carbonization and physical activation of Kevlar feedstock material procured from local industries, for effective electromagnetic (EM) shielding applications. The Kevlar fabric waste was directly carbonized under a layer of charcoal without any intermediate stabilization step at 800 °C, 1000 °C, and 1200 °C, with a heating rate of 300 °C/h and without any holding time. The physical and morphological properties of the activated carbon, influenced by carbonization process parameters, were characterized from EDX, X-ray diffraction, SEM analysis, and BET analysis. Furthermore, the electrical conductivity was analyzed. Finally, the potential application of the activated material for EM shielding effectiveness was analyzed at low (below 1.5 GHz) and high (2.45 GHz) frequencies. The phenomena of multiple internal reflections and absorption of electromagnetic radiations was found dominant in the case of activated carbon fabric produced at higher carbonization temperatures. [ABSTRACT FROM AUTHOR]