Search Results (231)

To investigate the combustion characteristics of moxa under a nitrogen atmosphere, this study employed an integrated approach combining experimental and theoretical analysis. Twelve moxa floss samples with different leaf-to-floss ratios, geographical origins, and storage durations were selected for thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FTIR) of their carbonized products in nitrogen environment. Through TG-DTG analysis, the thermal degradation patterns of the twelve moxa floss samples under nitrogen atmosphere were systematically examined to elucidate their pyrolysis behaviors, with particular emphasis on the influence of pyrolysis temperature and leaf-to-floss ratio on combustion characteristics. The pyrolysis process occurred in three distinct stages, with the most significant mass loss (120–430 °C) observed in the second stage. Higher leaf–fiber ratios and longer storage years were found to promote more complete pyrolysis. Kinetic analysis was performed to fit thermogravimetric data, establishing a reaction kinetic model for moxa pyrolysis. Results indicated that samples with higher leaf–fiber ratios required greater activation energy, while storage duration showed negligible impact. Notably, Nanyang moxa demanded higher pyrolysis energy than Qichun moxa. FTIR analysis identified the primary components of carbonized products as water, ester compounds, flavonoids, and cellulose. These findings suggest that moxa carbonization products retain chemical reactivity, demonstrating potential applications in adsorption and catalysis processes. Full article

Phosphorus flame retardants react with cellulose hydroxyl groups via esterification, enhancing the effectiveness of char formation, which is beneficial in terms of the search for bio-sourced flame retardants. The current work assessed the flammability of a new polymer synthesized by Michael 1,4-addition (rP) and modified with developed intumescent flame retardant systems (FRs), in which lignocellulose components, such as sunflower husk (SH) and peanut shells (PS), replaced a part of the synthetic ones. The thermal and thermomechanical properties of the rP, with 20 wt.% each from six FRs, were determined by thermogravimetric analysis (TG), differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA). Moreover, the flammability and evolved gas were studied with pyrolysis combustion flow calorimetry (PCFC) and thermogravimetric analysis connected with Fourier transform infrared spectroscopy tests (TGA/FT-IR). The effects were compared to those achieved for unmodified rP and a polymer with a commercially available intumescent flame retardant (IFR). The notable improvement, especially in terms of the heat release rate and heat release capacity, indicates that the system with melamine phosphate (MP) and peanut shells (PS) can be used to decrease the flammability of new polymers. An extensive analysis of the composition and geometry of the ground shells and husk particles preceded the research. Full article

The gasification of cellulose typically requires high temperatures (>600 °C) due to the thermal stability of levoglucosan, a major intermediate formed during pyrolysis. In this study, we investigated the gasification behavior of cellulose by combining infrared (IR) heating with low-power dielectric barrier discharge (DBD) plasma treatment. Cellulose filter paper was first pyrolyzed using localized IR irradiation (2 kW for 30 s), generating mist-like volatile products including levoglucosan. These volatiles were then exposed to DBD plasma (16–64 W for 1 or 3 min) under Ar flow. Despite the relatively low estimated gas temperatures below 240 °C in the plasma region, gas yields, including H₂ and CO, increased markedly with discharge power, reaching up to 72.6 wt% at 64 W for 3 min—more than four times that obtained with IR heating alone. These results indicate that DBD plasma facilitates the gasification of pyrolysis volatiles under significantly lower temperature conditions than those required in conventional thermal gasification. This approach may offer a route toward low-temperature biomass gasification with reduced tar, coke, and clinker formation. Full article

Gallium-modified Zeolite Socony Mobil-5 (ZSM-5) zeolites were synthesized using wetness impregnation and hydrothermal synthesis methods. The structural and acidic properties of the zeolites were characterized through an analytical instrument, which demonstrated that Gallium-modified HZSM-5 zeolites retain the Mobil five instructure (MFI) framework structure, but exhibit a reduction in Brønsted acid sites and a decrease in micropore size. The catalytic performance of these zeolites in the pyrolysis of cellulose biomass and polyethylene was tested. Compared with HZSM-5, Ga-modified HZSM-5 zeolites considerably increased monoaromatic yields while reducing alkanes production. In particular, gallium-impregnated HZSM-5 increased the monoaromatic yield from 37.6% for ZSM-5 to 43.2%, while hydrothermal synthesized Ga-HMFI reduced polyaromatic and alkane yields from 6.6% and 24.6% for HZSM-5 to 2.9% and 11.4%, respectively. These results indicated that Ga-modified HZSM-5 zeolites can improve the synergy between cellulose-derived oxygenates and polyethylene-derived olefins, enhancing the yield of petrochemical hydrocarbons compared to that predicted by theoretical calculations. Full article

Novel carboxymethylcellulose (CMC) films with liquid products of pyrolysis (LPP) from wood pine were produced. The obtained CMC-LPP films were plasticized with 5% glycerol. CMC-LPP films were a light brown colour with a characteristic smoky scent, and showed a higher oxygen permeability when compared to control film without the addition of the LPP. CMC-LPP exhibited high antioxidant activity (5 and 18 times higher than CMC films). Furthermore, the antibacterial activity of the CMC-LPP films was tested, showing a strong inhibiting growth effect on the seven tested human pathogenic bacteria. The new material had the most substantial bacteriostatic effect on Listeria monocytogenes, Salmonella typhimurium, and Pseudomonas aeruginosa. Introduction of LPP to plasticised CMC produces an eco-friendly material with biocidal effect and favourable mechanical and structural properties, which shows its potential for possible use in many industries. Full article

In this study, polymer composites based on a polypropylene (PP) matrix with the addition of cellulose and ES-40, used as a silica precursor, were investigated. These composites were designed to achieve enhanced biodegradability through the incorporation of bioavailable cellulose and to enable subsequent carbonization into carbon–silicon carbide systems. Rheological investigations revealed that the multicomponent mixtures exhibited pseudoplastic behavior over the shear rate range typical of injection molding, ensuring process stability without additional plasticization. Morphological analysis demonstrated that an optimal balance of PP, cellulose, and ES-40 promoted the formation of a three-dimensional network structure, leading to a significant increase in flexural modulus at the equal flexural strength despite some reduction in tensile strength. It was further shown that substituting fibrous cellulose with microcrystalline cellulose improved the composite homogeneity, thereby enhancing the density and mechanical properties, especially in systems with low polymer contents. Preliminary pyrolysis experiments indicated that these injection-molded composites can serve as precursors for fabricating bulk thermally stable products containing silicon carbide particles. The obtained results underscore the high potential of the developed materials for applications in conventional injection molding, the possibility of additive manufacturing, and processes requiring subsequent carbonization. Full article

The research investigates the thermal behavior of mixed systems based on natural and artificial cellulose fibers used as precursors for carbon nonwoven materials. Flax and hemp fibers were employed as natural components; they were first chemically treated to remove impurities and enriched with alpha-cellulose. The structure, chemical composition, and mechanical properties of both natural and viscose fibers were studied. It was shown that fiber properties depend on the fiber production process history; natural fibers are characterized by a high content of impurities and exhibit high strength characteristics, whereas viscose fibers have greater deformation properties. The thermal behavior of blended compositions was investigated using TGA and DSC methods across a wide range of component ratios. Carbon yield values at 1000 °C were found to be lower for blended systems containing 10–40% by weight of bast fibers, with carbon yield increasing as the quantity of natural fibers increased. Thus, the composition of the cellulose composite affects carbon yield and thermal processes in the system. Using the Kissinger method, data were obtained on the value of the activation energy of thermal decomposition for various cellulose and composite systems. It was found that natural fiber systems have three-times higher activation energy than viscose fiber systems, indicating their greater thermal stability. Blends of natural and artificial fibers combine the benefits of both precursors, enabling the deliberate regulation of thermal behavior and carbon material yield. This approach opens up prospects for the creation of functional carbon materials used in various high-tech areas, including thermal insulation. Full article

This work aimed to conduct a kinetic study of cotton stalks (CSs) through TGA to examine the impact of reaction conditions on bio-oil yield derived from CS slow pyrolysis using a tube furnace lab-scale reactor, as well as a characterization of bio-oil and biochar products. The iso-conversional approaches of Kissinger–Akahira–Sunose (KAS) and Flynn–Wall–Ozawa (FWO) were applied to estimate kinetic parameter activation energy (E_a) for the range of conversion degrees (α = 0.1–0.9). The kinetic results demonstrated that the average values of E_a for secondary pyrolysis were lower compared to those of primary pyrolysis; this could be explained by the fact that mainly cellulose degrades during primary pyrolysis, which requires more energy to be degraded. The pyrolysis findings indicated that the highest yield of bio-oil was 38.5%, which occurred at conditions of 500 °C and 0.5–1 mm size, while retention time showed an insignificant effect on pyrolysis oil. GC–MS analysis demonstrated that bio-oil is dominated by phenol compounds, which account for more than 40% of its components. SEM and XRD analyses emphasized that biochar is porous and has an amorphous shape, respectively. It can be concluded that these outcomes confirm that CSs have the potential to be a good candidate for a feedstock material for bioenergy production via the pyrolysis process. Full article

This review discusses the potential of emerging technologies, as well as their integration with conventional methods, to optimize the extraction of lignocellulosic compounds from cocoa pod hull (CPH), an agro-industrial residue that represents approximately 76% of the total weight of the fruit. CPH is primarily composed of cellulose, hemicellulose, lignin, and pectin. Emerging technologies such as microwave-assisted extraction, hydrothermal treatment, subcritical water, ionic liquids, deep eutectic solvents, and ultrasound treatment have proven effective in recovering value-added compounds, especially when combined with conventional techniques to improve process efficiency. Furthermore, the use of technologies such as high-voltage electric discharge (HVED) is proposed to reduce inorganic contaminants, such as cadmium, ensuring the safety of by-products. The CPH compounds’ applications include use in the food, pharmaceutical, cosmetics, agricultural, biopolymer, and environmental industries. The conversion of CPH to biochar and biofuels via pyrolysis and supercritical extraction is also discussed. The integration of technologies presents an opportunity to valorize CPH and optimize by-product development; however, as research continues, process scalability and economic viability must be assessed. Full article

The conversion of waste biomass into biochar through inert pyrolysis represents a promising strategy for carbon sequestration. However, biochar production is often accompanied by the release of small molecular chemical substances during pyrolysis, and the resulting biochar is susceptible to environmental degradation. To enhance the carbon retention rate of biochar during pyrolysis and its stability in the environment, this study explored the incorporation of various metal soluble salts (CaCl₂, Ca(H₂PO₄)₂, MgCl₂, FeCl₃) and clay minerals (quartz, goethite, bentonite, albite) with two types of waste biomass (phragmites and goldenrod) for pre-treatment to enhance both carbon retention and stability in the resulting biochar. Furthermore, to elucidate the regulatory mechanisms of minerals on biochar structural formation, the three primary components of raw biomass—hemicellulose, cellulose, and lignin—were individually mixed with the minerals at a ratio of 1:5 (mineral/biomass, w/w) to produce biochars for a comparative analysis. The experimental results demonstrated that metal soluble salts, particularly Ca(H₂PO₄)₂, exhibited a superior performance in enhancing biochar’s carbon retention compared to clay minerals. Specifically, Ca(H₂PO₄)₂ treatment resulted in a remarkable 15% increase in the carbon retention rate. Through K₂Cr₂O₇ oxidation simulating soil aging conditions, Ca(H₂PO₄)₂-treated biochar showed approximately 12% greater stability than the untreated samples. This enhanced stability was primarily attributed to the formation of stable chemical bonds (C–O–P and P–O), which facilitated the preservation of aromatic carbon structures and small molecular compounds including sugars, alcohols, and ethers. Mechanistic investigations revealed that Ca(H₂PO₄)₂ significantly influenced the pyrolysis process by increasing the activation energy from 85.9 kJ mol⁻¹ to 156.5 kJ mol⁻¹ and introducing greater reaction complexity. During the initial pyrolysis stage (<300 °C), Ca(H₂PO₄)₂ catalyzed depolymerization, ring-opening, and C–C bond cleavage in hemicellulose, enhanced cellulose depolymerization, and side-chain cleavage in lignin phenylpropanes. In the intermediate temperature range (300–400 °C), Ca(H₂PO₄)₂ facilitated carboxylate nucleophilic addition reactions and promoted cyclization to form aromatic carbon structures. The innovative aspect of this work is that minerals can increase both the yield and carbon retention rate of biochar. Furthermore, it reveals the mechanisms underlying the improvements in pyrolysis, providing a scientific basis and theoretical foundation for better displaying the carbon sequestration potential of biochar in future applications. Full article

Glucose is the most abundant monosaccharide as it is the primary unit of cellulose and starch, which are the more relevant feedstocks for biorefineries. Dehydration of glucose can lead to anhydroglucoses, whose interest has been increasing due to its potential industrial use. Commercial sulfonic polymer resins and a synthesized organic–inorganic mesoporous material were taken as Brønsted acid catalysts. High hexose conversion (up to 98%) and selectivity to anhydroglucoses (~80%) could be reached, turning this process into an alternative route to carbohydrate pyrolysis that presents an energy-intensive downstream. Hexose conversion to anhydroglucoses was related to the amount of acid sites, and the removal of one molecule of water from hexoses to produce anhydroglucoses was found as the preferential dehydration route over a bare Brønsted acid catalyst in anhydrous polar aprotic solvent (DMF) at mild conditions. Product distribution changed dramatically upon catalyst deactivation with HMF and fructose emerging as relevant products. It was suggested that an additional Lewis surface is produced during the deactivation process, probably arising from the formation of insoluble high molecular weight compounds in acidic media. Full article

This study explored the properties and pyrolysis characteristics of oxidatively torrefied cellulose to enhance biomass utilization and conversion. Cellulose was torrefied at 200–300 °C with oxygen concentrations of 0%–15%. The carbon content in cellulose could reach up to 53.06%, while the oxygen content decreased to 41.53% under the conditions of 300 °C and a 15% oxygen concentration. Meanwhile, its higher heating value (HHV) increased from 15.22 to 16.95 MJ/kg, improving the energy density and fuel quality. Both the carbon yield (CY) and energy yield (EY) of cellulose decreased noticeably with increasing oxygen concentrations at 300 °C, reaching minimum values of 46.33% and 51.05%, respectively, which were lower than the 64.5% and 71.85% observed under non-oxidative torrefaction. FTIR and XRD showed that higher temperatures and oxygen concentrations accelerated cellulose bond breaking and crystallinity disruption, enhancing thermochemical conversion. Oxidative torrefaction lowered the pyrolysis initiation temperature, with the most evident effect occurring at a 5% oxygen concentration of 300 °C. Increased oxygen concentrations altered pyrolysis products, with anhydrosugars rising then falling, and more furans, aromatics, and phenols produced. This study demonstrates that oxidative torrefaction effectively enhances the energy density of cellulose, showing promising potential for biomass utilization as a renewable fuel. Full article

This review provides an exploration of various catalytic pyrolysis techniques for bio-oil production, focusing on the effects of different pyrolysis methods (slow, fast, and flash pyrolysis) on bio-oil yield and composition. The review also discusses key factors influencing bio-oil production, including feedstock composition (cellulose, hemicellulose, and lignin), and the role of catalytic materials in enhancing yield and product selectivity. Three primary classes of catalysts—zeolites, carbonaceous materials, and metal oxides—are thoroughly examined, with a discussion on the differences between bulk catalysts and nanocatalysts. The paper highlights how these catalysts influence the formation of bio-oil components such as phenols, hydrocarbons, and oxygenated compounds. Furthermore, this review discusses recent advancements in catalyst design and modifications to optimize bio-oil production. This review provides the latest advancements in catalytic pyrolysis, emphasizing the correlation between catalyst properties and the resulting products. It aims to offer valuable insights into the future potential of catalytic pyrolysis for efficient biomass conversion and sustainable biofuel production. Full article

With the overuse of fossil fuels, people are looking for alternatives. This is an area where biofuels have received a lot of attention. Studies have also shown that a large variety of liquid fuels of commercial interest can be obtained via lignin valorization. Lignin is rich in aromatic ring structures and can be used as a sustainable raw material to produce high-value energy. Therefore, progress in the preparation of liquid fuels from lignin by pyrolysis, hydro-processing, and oxidation is analyzed in this review. Nevertheless, due to the three-dimension network structure of lignin, there are many barriers that need to be surmounted before utilizing it, such as its complex connection with cellulose and hemicellulose, which makes its separation difficult. In this paper, different pretreatment methods are summarized for separating lignin from other two components. Finally, the challenges in future trends of lignin valorization are summarized and outlined. It is clear that the construction of efficient separation and catalytic systems will be the focus of future research in this field. Full article

EFB is a biomass waste primarily generated in Southeast Asia, and its pyrolysis enables both waste management and conversion into valuable products. In pyrolysis, the heating rate is a crucial factor; however, studies on its influence on EFB are extremely limited. This study investigates the pyrolysis characteristics of EFB by analyzing product properties based on reaction temperature and heating rate. TGA showed that the thermal decomposition of EFB begins at approximately 210 °C and is largely complete by 400 °C. Furthermore, kinetic analysis using TGA data, applying both differential and integral methods, revealed distinct trends. Through pyrolysis experiments using a fixed-bed reactor, the yield analysis of products under varying reaction temperatures and heating rates demonstrated that higher temperatures promote pyrolysis, leading to a decrease in biochar yield and an increase in gas product yield. For liquid products, a higher heating rate suppressed secondary reactions and led to an increase in the yield of the aqueous phase. Gas product characterization revealed that CO and CO₂ formation began simultaneously at approximately 270 °C. GC-MS analysis of the liquid products recovered under different pyrolysis conditions showed that most compounds contained oxygen, originating from hemicellulose, cellulose, and lignin. Additionally, FT-IR analysis of the biochar confirmed that oxygen-containing functional groups decomposed as pyrolysis progressed, and the presence of turbostratic carbon and crystallinity influenced by trace inorganic elements was identified. Full article