Increasing Pyrolysis Temperature Research Articles

Molecular dynamics study of waste tire pyrolysis: Focus on intermediate product evolution and sulfur migration law

With the rapid development of the automotive industry, the large number of waste tires poses significant environmental and health pressures. Pyrolysis technology offers a way to resourcefully utilize waste tires by converting them into pyrolysis oil, pyrolysis gas, and pyrolysis char, which has promising application prospects. However, there are still considerable challenges in the application of this technology, such as unclear reaction mechanisms and the high sulfur content of the products, which limit its practical implementation. Although some research has elucidated the pyrolysis mechanisms, there remain significant gaps in understanding the evolution paths of key intermediate and final products, as well as the detailed migration and transformation patterns of sulfur. This study uses reactive molecular dynamics simulation to investigate the pyrolysis process of tires. A three-dimensional polymer molecular model was constructed to study the pyrolysis process of waste tires at different temperatures, focusing on the evolution of key products, intermediate products, and sulfur-containing components. The results indicate that CH4 and ·CH3 radicals collide with unsaturated hydrocarbons through carbon-hydrogen transfer reactions and radical chain reactions, leading to polymerization. During the initial stage of pyrolysis, sulfur primarily exists in the form of sulfur-containing hydrocarbons (CHS). As pyrolysis progresses, the quantity of CHS decreases. With increasing pyrolysis temperature, the proportion of sulfur in the S form far exceeds that of CHS. At a pyrolysis temperature of 3000 K, the proportion of S is 64 %, while the proportion of CHS is 23 %.

Effects of pyrolysis temperatures on the structural properties of straw biochar and its adsorption of tris-(1-chloro-2-propyl) phosphate

To investigate the effect of pyrolysis temperature on the adsorption behavior of the emerging organic pollutant tris-(1-chloro-2-propyl) phosphate (TCIPP) on biochar, corn stover was used as raw materials to prepare biochars at different pyrolysis temperatures (250, 350, 500, 700 °C) through limited oxygen carbonization. Elemental analysis, Boehm titration, FTIR, XPS, and other analytical methods were used to reveal the effect of pyrolysis temperature on the physicochemical properties of biochar and its mechanism of TCIPP adsorption. The results showed that the pyrolysis temperature had a significant impact on the physicochemical properties of biochar. As the pyrolysis temperature increases, the specific surface area of biochar rises from 3.083 m2/g to 435.573 m2/g, the pH value increases from 6.60 to 10.66, the mass percentage of C increases from 63.10 to 80.58%, and the mass percentage of O decreases from 26.42 to 9.20%. Additionally, the hydrophobicity and aromaticity of biochar also increase with rising pyrolysis temperature, while its polarity decreases. Boehm titration, FTIR, and XPS analysis showed that the total amount of functional groups on the surface of biochar decreased relatively with increasing temperature. Functional groups such as -OH, C = C/C = O, and C-O-C participated in the adsorption of TCIPP on biochar, and ester groups were produced after adsorption. The adsorption process of TCIPP on biochar fits best with the pseudo-second-order equation, indicating that the adsorption process is mainly chemical adsorption, and the main rate-controlling stage is intraparticle diffusion. The isothermal adsorption results were more in line with the Temkin model, indicating that the adsorption process of TCIPP on biochar was mainly surface adsorption. As the pyrolysis temperature increases, the maximum adsorption capacity of biochar increases from 0.8837 mg/g to 2.2574 mg/g. The adsorption process of TCIPP on biochar mainly included pore filling, hydrogen bonding, P-π interaction, hydrophobic interaction, and electrostatic attraction. Among them, pore filling, P-π interaction, and hydrophobic interaction were significantly enhanced with increasing temperature, while hydrogen bonding was relatively weakened. This study will provide a theoretical basis and technical support for the removal of TCIPP from water using biochar adsorption.

Chemical and Physical Properties of Selected Biochar Types and a Few Application Methods in Agriculture

Biochar, a carbon-rich by-product of organic matter pyrolysis, has a variety of physiochemical properties beside a variety of applications. This review highlights some physical and chemical characteristics of herbaceous, woody, and sewage waste biochar under different pyrolysis conditions, as well as soil and foliar applications of biochar. The controlling role of pyrolysis temperature was the reason for selecting the discussed biochar types in the study. This review concludes that increasing pyrolysis temperature mainly raised the values of some chemical properties of the biochar, such as pH, electrical conductivity (EC), ash content, total phosphorus (TP), and a few values of physical properties like porosity and specific surface area (SSA). On the other hand, yield and total nitrogen (TN) decreased with rising pyrolysis temperature. Among biochar application methods to soil, mixing biochar with soil before planting is one of the best methods of application, and in most cases, biochar reapplication improved soil properties, while foliar application of biochar has positive effects on plant growth and yield parameters, ranging from low rates to the highest ones.

Porous biochar production from microwave pyrolysis of sugarcane bagasse biomass with KOH addition

ABSTRACT Biomass-based porous carbons have diverse structures and typically exhibit good multifunctionality. Therefore, compared to direct combustion, using pyrolysis to convert agricultural waste into biochar is an environmentally friendly and effective treatment method. Preparing biomass-derived porous carbon materials (PCMs) through microwave is challenging, as biomass rarely absorbs microwave energy and necessitates the inclusion of additional microwave absorbers. In this study, a silicon carbide crucible was designed to simplify the microwave pyrolysis process, and sugarcane bagasse-based porous carbon (GZKM) was prepared using a microwave pyrolysis coupled with KOH activation method without adding additional microwave absorbers. A detailed study was conducted on the yield, surface morphology, and pore structure of biochar obtained from different temperatures (700, 750, 800, 850, and 900 °C) and different mass ratios of sugarcane bagasse to KOH (0, 4:1, 2:1, 1:1, and 1:2). The results indicated that as the pyrolysis temperature and KOH addition increased, the yield of biochar gradually decreased from a highest value of 31.41 wt% to a lowest value of 11.8 wt%. The specific surface area (SBET) of GZKM initially increased and then decreased with the increase in pyrolysis temperature and KOH mass, reaching a maximum value of 889.41 m2/g. The results of this study can provide guidance for the reuse of sugarcane bagasse and the preparation of porous biochar, and can also be applied in fields such as electrocatalysts, batteries, biomedical materials, and wastewater treatment.

Sugarcane straw biochar: effects of pyrolysis temperature on barite dissolution and Ba availability under flooded conditions

AbstractReductive dissolution of barium (Ba) sulfate in wetland soils may increase Ba bioavailability in the environment, yet no information is available regarding Ba remediation using biochar. This study investigated the effectiveness of sugarcane (Saccharum officinarum) straw biochar pyrolyzed at 350 °C (BC350), 550 °C (BC550), and 750 °C (BC750) in inhibiting barite dissolution and, consequently, Ba availability in a soil artificially spiked with barite and flooded for 365 days. Increasing pyrolysis temperature alters the carbon structure, and increases dehydration and depolymerization, resulting in more stable biochar that releases less DOC (8.6-fold decrease from BC350 to BC750). Additionally, high-temperature biochar (BC750) had 1.7 times higher carbon (C) content, 2.4 times higher ash content, and a 13.1 times greater specific surface area (SSA) than low-temperature biochar (BC350). Amending soil with BC750 increased pH but did not promote reducing conditions, and thus did not promote barite dissolution. Conversely, greater DOC in low-temperature biochar, particularly BC350, favored reducing conditions and increased barite dissolution by 23%, with BC550 also showing an 18% increase. This enhancement led to a greater pool of Ba sorbed into more labile exchangeable sites. In summary, pyrolysis temperature affects biochar attributes, which in turn influences the soil geochemical environment and Ba speciation. Low-temperature biochar (BC350) shows potential as an amendment to increase the bioavailable Ba pool in assisted remediation programs, such as biochar-assisted phytoremediation. Graphical Abstract

Synergistic effects of feni bimetal-doped biochar on oxygen evolution reaction kinetics: A one-step, low-temperature pyrolysis approach

As the hydrogen energy sector progresses, water electrolysis technology played a crucial role in producing green hydrogen. A major challenge in this endeavor lied in the oxygen evolution reaction (OER), where the overpotential has consistently been high leading to an increase in the energy demand. This study developed a one-step pyrolysis technique to transform metal-supported biomass into FeNi/NC catalysts having enhanced crystallinity and defect sites. This process without activation step using strong acids or bases reduced the operational procedures and the treatment of intermediate products, which reduced the technical difficulty. As the pyrolysis temperature increases, the metal ions in the biochar gradually formed stable metal oxides, which catalyze the alkaline OER and markedly boosted catalytic efficiency. Crucially, the abundance of lattice oxygen and oxygen vacancies in the catalyst played a key role in enhancing the OER kinetics. Notably, the catalyst pyrolyzed at 750 °C demonstrated good performance, with an overpotential of 270 mV at a concentration of 10 mA cm−2 of the density of current, which was superior to RuO2(η10=315 mV) and IrO2(η10=300 mV). Overall, this study reported an approach for the fabrication of high-performance OER catalysts and the strategic utilization of biomass resources for application in clean energy technologies.

Engineering cellulose nanofibril aerogel for reinforcing polymethyl methacrylate with superior mechanical strength, high transparency, and improved thermal stability

In this study, a new strategy for preparing cellulose nanofibers/polymethyl methacrylate (CNF/PMMA) composite with high strength and high transmittance was developed. The UV curing technique was adopted to induce the polymerization of MMA and the grafting modification of methacryloylated CNF aerogel (CNFMA). The compatibility between CNF aerogel and PMMA was significantly improved through the grafting modification of CNF aerogel. The cold ultraviolet photopolymerization strategy makes the polymerization reaction much milder. The transmittance of the CNFMA/PMMA composite was 86.45 %, showing only a slight reduction compared to PMMA. Its tensile strength increased to 69.21 MPa, about twice that of PMMA, and 1.5 times that of CNFpure/PMMA, proving the interaction between CNF and PMMA was greatly enhanced due to the successful grafting of PMMA onto the surface of CNF. The glass transition temperature is 108.1 °C, which increased by nearly 20 %. The thermal stability has also been improved, as reflected by a 10 % increase in the initial pyrolysis temperature. Overall, this work provides a mild and green preparation method for CNF/PMMA composites, making them suitable for applications in the field of high-strength organic glass.

Comprehensive evaluation of the physicochemical properties and pyrolysis mechanism of products from the slow pyrolysis of waste coffee shells

Slow pyrolysis is an efficient method for converting agricultural and forestry wastes into valuable resources, thereby addressing energy shortage and environmental pollution. In this study, a slow-pyrolysis experiment of coffee shells (CS) at 450–850 °C was conducted in a tube furnace. The resulting pyrolysis products were comprehensively characterized via FTIR, Raman spectroscopy, nitrogen adsorption analysis via BET theory, SEM, XPS, and PY-GC-MS. Moreover, the pyrolysis reaction mechanism and N transformation pathway of CS were proposed. The results showed that with the increase in pyrolysis temperature, the yield of biochar gradually decreased, and the yield of biogas gradually increased. At 850°C, the yields of biochar, bio-oil and biogas of CS were 27.13, 35.16 and 37.71 %, respectively (on a dry, ash-free basis). The bio-oil yield was highest at 550 °C, reaching 35.7 %. Notably, biochar exhibited favorable characteristics such as high specific surface area and porosity, demonstrating its potential as both a biomass fuel and an adsorption material. Acetone (78.30 %) and caffeine (8.29 %) was the predominant substance in bio-oil. Biogas was predominantly composed of CO2, CO, CH4 and H2. The pyrolysis process of CS mainly involved the degradation of macromolecules into small molecules, the repyrolysis of small molecules, dehydrogenation, deoxygenation, alkylation, isomerization, and self-condensation. These results provide a theoretical basis for the recycling of waste biomass CS, which has environmental protection significance and economic value.

Bleached cellulose biochars as a sustainable alternative for oilfield-produced water (OPW) treatment and environmental remediation

Eucalyptus, a renewable and fast-growing raw material widely used in the paper industry, has great potential for new applications beyond papermaking. Bleached eucalyptus pulp, traditionally used in the pulp industry, has proved to be a promising alternative for removing complex organic compounds such as naphthenic acids (NAs), often found in oil-produced water (OPW). This study aimed to optimize the production of biochars from bleached eucalyptus pulp through pyrolysis at 700, 800, and 900 °C and to correlate the resulting properties with the ability to adsorb NA at low concentrations and in acidic and alkaline media. The research explores realistic environmental scenarios where naphthenic acids may be present in dilute concentrations after initial treatments. The biochars were characterized by their micro and mesoporous structures, amorphous structures, and distinct functional groups and were evaluated in simulated effluents. Biochar B900 reached a maximum adsorption capacity of 35 mg/g at pH 4 and 25 °C, excelling in acidic environments, while at pH 8, biochar B700 showed better performance. The PVSDM model revealed that mass transfer and pore diffusion coefficients increased with increasing pyrolysis temperature. The Langmuir model was the best fit for the experimental data. The biochar produced at 900 °C had the highest specific surface area (1,041.55 m2/g) and pore volume (0.56 cm3 g−1), favoring its adsorption capacity. Although the biochar shows good initial efficiency, the progressive reduction in adsorption capacity over the cycles suggests limited reusability, highlighting the need for optimization in the regeneration process to improve its economic viability in wastewater treatment.

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

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

Performance of Bioenergy Production from Durian Shell Wastes Coupled with Dye Wastewater Treatment

Adsorption using biochar is a high-efficient method for removing dyes from wastewater, and it has become a hot research topic in recent years. Biochar produced from organic wastes through pyrolysis is a promising way to combine bioenergy recovery and dye removal. In this study, durian shell (DS) was used as a feedstock for biochar and bio-oil production under different pyrolysis temperatures (400, 500, and 600 °C) for bioenergy recovery. Then, the biochar was applied as the absorbent for methylene blue (MB) removal from wastewater under batch and continuous experiments. It was found that the bio-oil production was slightly affected by temperature, while the productivity of biochar decreased from 42.05% to 30.65% with the increase in pyrolysis temperature from 400 to 600 °C. Compared with the biochar produced at 500 °C (DS-500) and 600 °C (DS-600), the biochar obtained at 400 °C (DS-400) exhibited higher MB removal efficiency and adsorption capacity under various pH conditions due to the superior microstructure. A high pH condition was beneficial for the adsorption process with DS-400. Additionally, the MB removal efficiencies increased with the increase in biochar dosage by providing more activated sites. A high MB content can promote the adsorption process, but a too high MB content negatively affects the removal efficiency due to the sorption saturation. Adsorption processes are more likely to match a pseudo-second-order model by chemical reactions. In the long-term continuous experiment, MB can be effectively removed to match the discharge standard by DS-400. This study provided a sustainable pathway for organic waste disposal and dye wastewater treatment.

Conversion of acidified lignin containing sulfur discharged from a biorefinery process into neutralized biochar: Characterization and metal adsorption

The objectives of this study were to produce biochars using sulfur-rich acidified lignin discharged from a biorefinery process and to evaluate their physicochemical properties and Pb adsorption capacity. As the pyrolysis temperature increased, the lignin acidified by the desulfurization process was converted to neutralized biochar (LBC), which exhibited high carbon content and stability. The carbon content of biochar manufactured at a pyrolysis temperature of 600 °C or higher was over 90 % and showed no significant difference, and their surface structures were found to be different, as revealed through XRD and FTIR analyses. The adsorption capacity of Pb by LBC increased with increasing pyrolysis temperature, and their adsorption capacity was well described by the pseudo-second-order model and the Langmuir isotherm adsorption model. In particular, the internal diffusion effect on the adsorption capacity of Pb was greater for LBC900 than for LBC600. In complex heavy metal solutions, LBC selectively exhibited high affinity for Pb, while the adsorption capacity of other metals was significantly reduced. The adsorption mechanism of Pb by LBC was verified through various analytical methods, and these results demonstrated that the adsorption of Pb by LBC was influenced by functional groups existing on the surface and inside of LBC and by some cation exchange.

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

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

Adsorption of per- and polyfluoroalkyl substances on biochar derived from municipal sewage sludge

Granular activated carbon (GAC) and ion exchange resin (IXR) are widely used as adsorbents to remove PFAS from drinking water sources and effluent waste streams. However, the high cost associated with GAC and IXR generation has motivated the development of less expensive adsorbents for treatment of PFAS-impacted water. Thus, the objective of this research was to create an economically viable and sustainable PFAS adsorbent from sewage sludge. Stepwise pyrolysis at temperatures from 300 °C to 1000 °C yielded biochars whose specific surface area (SSA) and porosity increased from 41 to 148 m2/g, and from 0.062 to 0.193 cm3/g, respectively. On a per organic char basis, the SSA of the biochar was as high as 1183 m2/g, which is comparable to commercially-available activated carbons. The adsorption of perfluorooctane sulfonic acid (PFOS) on sludge biochar increased with increasing pyrolysis temperature, which was positively correlated with increasing porosity and SSA. When 1000 °C processed biochar was tested with a mixture of eight PFAS, preferential adsorption of longer carbon chain-length species was observed, indicating the importance of PFAS hydrophobic interactions with the biochar and the availability of a wide range of mesopores. The adsorption of each PFAS was dependent upon both chain length and head group, with longer chain-length species exhibiting greater adsorption than shorter chain-length species, along with greater adsorption of species with sulfonic acid head groups compared to their chain length counterparts with carboxylic acid head groups. These findings demonstrate that biochar derived from municipal solid waste can serve as a cost-effective and sustainable adsorbent for the removal of PFOS and PFAS mixtures from source waters. The circular economy benefits and waste reduction potential associated with the use of sewage sludge-derived biochar supports the development of a viable sludge-derived biochar for the removal of PFAS from water.

Aspects of thermal utilization of organic poultry waste

Relevance. Currently, poultry farming, as part of the agro-industrial complex, is showing strong growth, which leads to an increase in the generation of organic waste. Chicken manure is a problematic organic waste from poultry farming in terms of its quantity, environmental hazard and moisture content. On the other hand, chicken manure is a potential renewable source of phosphorus. The use of chicken manure as a technogenic deposit of phosphorus will improve the level of environmental and food security. Aim. Research of influence of parameters of plasma and pyrolysis treatment of chicken manure on waste weight loss and phosphorus content in biochar. Methods. Experimental studies of the treatment of chicken manure with microwave plasma and induction pyrolysis; determination of the mass fraction of moisture during drying and loss of waste mass during disposal by the gravimetric method; determination of phosphorus in biochar using the Denizhe colorimetric method modified by A. Malyugin and S. Khrenova. Results and conclusions. The author has carried out the experimental studies on the treatment of chicken manure with microwave plasma and induction pyrolysis. It was shown that effective ways to reduce the mass of chicken manure and prevent environmental pollution are the treatment of manure with microwave plasma and its induction pyrolysis. It was established that when chicken manure is processed in microwave plasma in an inert environment at temperatures up to 1560°C, the mass of waste is reduced by 92.76% with an exposure duration of 7 minutes. At the same time, the content of P2O5 in biochar is up to 52.2 g/100 g of biochar. Further exposure to plasma leads to vitrification of the waste. As the time of treatment of chicken manure with microwave plasma increases, the loss of waste mass grows exponentially. Induction pyrolysis of chicken manure in an inert environment at a temperature of 1000°C makes it possible to reduce the mass of waste by 92.30%. P2O5 content in biochar grows with increasing pyrolysis temperature and amounts to 12.64 g/100 g of biochar. Biochar obtained by treating chicken manure with microwave plasma and induction pyrolysis can be considered as a source of phosphorus. The results obtained indicate the possibility of utilizing chicken manure using microwave plasma and induction pyrolysis.

Effect of Rice Biochar on Typical Cadmium, Lead and Zinc Form in Contaminated Soil in Northwest Guizhou Province, China

This study was conducted in Hezhang County, Bijie City, Guizhou Province. The soil in the zinc smelting area has been contaminated with cadmium, lead, and zinc. Therefore, these elements are the focus of this research. Rice husk biochar was used as the passivation material. The Fourier infrared spectrum was utilized to study the biochar’s morphology, element content, mineral composition, structure, and surface functional groups. Moreover, the physical and chemical properties of the biochar were analyzed to explore its passivation effect. Biochar is beneficial in the cleaning of cadmium, lead, and zinc minerals and can be used for the passivation of heavy metals in contaminated soil. This study aims to understand the detailed mechanism behind this process and provide experimental data and ideas for pollution control. The results indicate that the biochar contains many functional groups, including -OH, C-H, C-O, C=O, C=C, and C-O-C. It also consists of a significant quantity of potassium salt, calcite, and quartz. Biochar has a noticeable pore structure, and as the pyrolysis temperature increases, the pore structure becomes more developed and thinner, with a smooth surface. The main minerals in the soil are quartz, mica, zeolite, illite, and chlorite. The aromatic degree of biochar increased with pyrolysis temperature. In contrast, the aromatic degree and polarity first increased and then decreased. The 0.2-0.45 mm biochar exhibited the best passivation effect on cadmium, lead, and zinc.

Study on the properties and components of solid-liquid products by co-pyrolysis of sludge and cotton stalk

The effects of sludge content and pyrolysis temperature on the pyrolysis process and product properties were studied through the co-pyrolysis of sludge and cotton stalk. Multi-objective fuzzy hierarchical analysis was used to analyze the multiphase properties of pyrolysis products, and describe the internal relationship between pyrolysis conditions and product properties. It has been proved using kinetic calculation that the mass ratio of sludge and cotton stalk is higher than 1:2 required the lower pyrolysis activation energy. According to the comparison between experimental and theoretical results, the addition of sludge is beneficial to increase the bio-oil yield. In terms of product performance, the addition of sludge and increase of pyrolysis temperature both can improve the specific surface area, pore volume of biochar and the pH value of bio-oil, reduce the total acid content, increase the total phenol content and optimize calorific value of bio-oil. The specific surface area of biochar, calorific value of bio-oil, total phenol content and pH were evaluated by multi-objective decision analysis method, the optimum process condition of sludge: cotton stalk = 2:1 at 600 ℃. Under the conditions, the specific surface area of biochar is 57.40 m2/g, the pH of the bio-oil is 8.06, the total acid content is 5.94 mg/g, the calorific value is 27.18 KJ/g and the total phenol content is 47.32 mg/g, respectively. Compared to the pyrolysis product of cotton stalks, the specific surface area is increased almost 20 times, the calorific value is increased by 13 %, the total acid content is decreased by 95 %, and the total phenol content is similar. This study proposed a preparation process of bio-oil with high performance, and provided a theoretical basis for the subsequent co-pyrolysis research.

Rapid pyrolysis of cellulose: Revealing the role of volatile matter and char structure evolution

The complexity of the cellulose structure hinders its energy conversion and utilization. Pyrolysis is not only an independent thermochemical conversion technology but also a necessary stage in the gasification process. The real-time capture of volatile components in cellulose pyrolysis is difficult, and the evolution of char structures is lacking, which is extremely challenging. In this work, elemental analysis, industrial analysis, thermogravimetric analysis, infrared spectroscopy (FTIR), Raman spectroscopy (Raman), and X-ray diffraction spectroscopy (XRD) were used to characterize the raw materials and products. Combined with rapid pyrolysis experiments, the pathways of cellulose pyrolysis volatiles and char structure evolution were explored. Dehydrated sugars are the initial products formed below 350 ℃, which quickly dehydrate to form furan compounds at 400 ℃ and then break CC bonds at 600 ℃ to generate fatty aldehydes, ketones, and carboxylic acids. Biochar generated at low temperatures (<300°C) has strong lipid solubility. An increase in pyrolysis temperature leads to a continuous decrease in the content of H and O in biochar, which destroys its functional groups and physical structure, and ultimately tends to form graphite-type char with aromatic structures. Based on the correlation between the volatile matter release characteristics and the evolution of the semichar structure, a cellulose pyrolysis pathway was established, providing theoretical support for the high-value utilization of cellulose.

Impact of nickel and alkaline earth metals interaction on sustainable carbon nanotubes generation from plastic face masks via catalytic pyrolysis

The one-pot synthesis of carbon nanotubes (CNTs) emerges as a promising approach for plastic valorization, owing to its simplicity and scalability. However, limited attention has been given to catalyst design for this method, particularly regarding the influence of Group 2 alkaline earth metal elements (X) on the Ni-based catalyst activity. This study investigates the impact of X on the catalytic activity of Ni towards sustainable CNTs synthesis using plastic face masks. The findings revealed that X influenced the carbon yield of NiMo-X catalysts and the morphology of the resultant carbon nanomaterials. Notably, NiMo-Ca demonstrated the highest carbon yield, whereas NiMo-Mg and NiMo-Ba exhibited the lowest. Furthermore, NiMo-Mg tends to produce clean and thin CNTs, while NiMo-Ba tends to yield carbon flakes with numerous irregular cokes. In addition to the effect of Ni crystallite size, which influences the transition from tubular to flake-like carbon structures, environmental factors are also considered. Specifically, NiMo-Mg generated a high CO2/CH4 environment, while NiMo-Ba exhibited slower catalytic cracking of polymeric chains from face masks, both of which were unfavorable for CNTs growth. Conversely, NiMo-Ca facilitated higher carbon recovery, likely due to its creation of a low CO2/CH4 environment via CO2 methanation. Optimization studies indicated that increasing pyrolysis temperatures and durations lead to reduced carbon yield, while cyclic pyrolysis of face masks up to five iterations enhances the reusability of NiMo-X catalysts with improved carbon recovery. Overall, this study provides valuable insights into the early pyrolytic gas formation and carbon nucleation phase, which are influenced by the surface Ni fraction and Ni polarization, as well as the later CNTs growth phase, which is related to the Ni crystallite size.

Nitrogen-rich carbon nitride with heptazine phase controlled by pyrolysis temperature towards photocatalytic U(VI) reduction

Photocatalytic process is a new and efficient technology, which has great potential in the U(VI) reduction process. Nitrogen is volatile at high temperatures, so its synthesis reaction is significantly influenced by pyrolysis temperature. Herein, a series of nitrogen-rich carbon nitride with different nitrogen content and different catalytic properties were prepared by changing the pyrolysis temperature from 450 °C to 650 °C. With the increase of pyrolysis temperature, the nitrogen content decreases continuously, and the triazine ring, tetrazine ring and azo bond generated by low temperature pyrolysis are gradually replaced by heptazine ring and nitrogen single bond. The nitrogen-rich carbon nitride synthesized at 550 °C has the best reducing activity for U(VI) reduction, which is attributed to the good cavity structure, narrow light absorption band gap and high electron transport channel. These results can provide guidance for regulating the electron transport structure of the nitrogen-rich carbon nitride to achieve enhanced photocatalytic activity.