Biomass Conversion Research Articles

Improved Hydrothermal Conversion of Pea Pod Biomass for Production of Platform Chemicals with Organic Acid Catalysts

Agro-industries produce over 2 billion tons of agricultural waste annually, including by-products like bagasse, molasses, seeds, stems, leaves, straw, and shells. The use of agro-industrial waste is a way to reduce the impact of industrial processes on the environment. The pea pod is a biomass with a high concentration of cellulose, hemicellulose and some lignin; therefore, it can be used to produce platform chemicals by means of a hydrothermal process. There is limited research on the hydrolysis of pea biomass, but it has been shown to obtain high yields. This study analyzed the effectiveness and selectivity of the hydrothermal process using pea pod biomass with a particle size of 0.5 mm at 180 °C for one hour. A 500 mL reactor was used, with a biomass-to-acid solution ratio of 1:20. The concentration of the acid solution was 0.02 M. The concentrations of sugar, formic acid, levulinic acid, HMF, and furfural produced were measured. Among the catalysts studied, adipic acid catalysis showed the highest yield of 65.16%, with 37.09% of sugar, 16.37% of formic acid, and 11.71% of levulinic acid. On the other hand, the catalysts with chloroacetic acid, butyric acid, anthranilic acid, and phthalic acid were less effective but demonstrated selectivity for sugar production, proving that the liquid phase obtained using the catalyst with those acids can be used as carbon sources for a fermentation process. In general, when comparing the process with or without the use of a catalyst, it is observed that with a catalyst in the reaction, the amount of HMF and furfural produced is reduced and the selectivity with respect to sugar production is increased.

Coupling Photocatalytic Hydrogen Production with Key Oxidation Reactions.

Hydrogen represents a clean and sustainable energy source with wide applications in fuel cells and hydrogen energy storage systems. Photocatalytic strategies emerge as a green and promising solution for hydrogen production, which still reveals several critical challenges in enhancing the efficiency and stability and improving the whole value. This review systematically elaborates on various coupling approaches for photocatalytic hydrogen production, aiming to improve both efficiency and value through different oxidation half-reactions. Firstly, the fundamental mechanism is discussed for photocatalytic hydrogen production. Then, the advances, challenges, and opportunities are expanded for the coupling of photocatalytic hydrogen production, which focuses on the integration of value-added reactions including O2 production, H2O2 production, biomass conversion, alcohol oxidation, and pollutants treatment. Finally, the challenges and outlook of photocatalytic H2 production technology are analyzed from the aspects of coupling hydrogen production value, photocatalyst design and reaction system construction. This work presents a holistic view of the field, emphasizing the synergistic benefits of coupled reactions and their practical application potential, rather than focusing on catalysts or single reaction systems. This review provides valuable references for the development and application of photocatalytic hydrogen production in energy conversion and environmental conservation through sustainable, eco-friendly and economic pathways.

Coupling Photocatalytic Hydrogen Production with Key Oxidation Reactions

AbstractHydrogen represents a clean and sustainable energy source with wide applications in fuel cells and hydrogen energy storage systems. Photocatalytic strategies emerge as a green and promising solution for hydrogen production, which still reveals several critical challenges in enhancing the efficiency and stability and improving the whole value. This review systematically elaborates on various coupling approaches for photocatalytic hydrogen production, aiming to improve both efficiency and value through different oxidation half‐reactions. Firstly, the fundamental mechanism is discussed for photocatalytic hydrogen production. Then, the advances, challenges, and opportunities are expanded for the coupling of photocatalytic hydrogen production, which focuses on the integration of value‐added reactions including O2 production, H2O2 production, biomass conversion, alcohol oxidation, and pollutants treatment. Finally, the challenges and outlook of photocatalytic H2 production technology are analyzed from the aspects of coupling hydrogen production value, photocatalyst design and reaction system construction. This work presents a holistic view of the field, emphasizing the synergistic benefits of coupled reactions and their practical application potential, rather than focusing on catalysts or single reaction systems. This review provides valuable references for the development and application of photocatalytic hydrogen production in energy conversion and environmental conservation through sustainable, eco‐friendly and economic pathways.

Transforming Lignocellulosic Biomass into Biofuels: Recent Innovations in Pretreatment and Bioconversion Techniques

Abstract: This scholarly review investigates contemporary advancements in the conversion of lignocellulosic biomass to biofuels, emphasizing innovative pretreatment and bioconversion technologies that aim to surmount the intrinsic challenges associated with the processing of this complex biomass. Lignocellulosic materials, which are predominantly comprised of cellulose, hemicellulose, and lignin, represent a renewable and plentiful source for biofuel production; however, their structural complexity necessitates sophisticated methodologies for the effective degradation of resistant components. The review scrutinizes a variety of pretreatment methodologies, encompassing physical, chemical, and burgeoning techniques such as plasma-assisted processing, which are engineered to augment cellulose accessibility for enzymatic hydrolysis. Additionally, it elucidates the progress made in bioconversion processes, concentrating on enzymatic hydrolysis, microbial fermentation, and consolidated bioprocessing (CBP), wherein recent endeavors in genetic engineering are refining microbial strains to enhance yield and efficiency. By addressing economic, technological, and environmental challenges, this article emphasizes the role of integrated biorefineries and innovative biotechnologies in facilitating scalable and cost-effective production of lignocellulosic biofuels. Prospective research trajectories include the formulation of sustainable pretreatment techniques and the advancement of synthetic biology to fully harness the potential of lignocellulosic biomass as a renewable energy resource. Ultimately, this review accentuates the significance of lignocellulosic biofuels as a feasible alternative to fossil fuels, thereby contributing to energy sustainability and climate change mitigation through diminished carbon emissions

Utilization of benzoic acid-based green deep eutectic solvents for the fractionation of lignocellulosic biomass.

The fractionation of lignocellulose utilizing green solvents is essential for the effective operation of biorefineries. In this study, a deep eutectic solvent (DES) system composed of benzoic acid (BA, hydrogen bond donor) and choline chloride (ChCl, hydrogen bond acceptor) was fabricated and successfully applied to the lignocellulose fractionation. The DES has low toxicity and little pollution. In this system, 67.8 % of lignin and 91.2 % of hemicellulose in poplar were removed, leaving 95.8 % of cellulose intact as solid residue. Due to the removal of the amorphous components, crystallinity of cellulose-rich water-insoluble solid (CIS) substantially increased from 55.6 % to 68.6 %, and CIS was used as feedstock for nanocrystalline cellulose preparation with excellent properties. The results showed that the obtained lignin had similar properties to CEL by GPC, FT-IR, 2D-NMR and TGA. A high-purity lignin rich in G units was recovered with a well-preserved structure, which has β-O-4 linkage content up to 53.01 %, low molecular weight, low polydispersity (1.99). Finally, the hydrolyzate can be used for fermentation. This study demonstrated that BA is suitable for DES design with excellent properties on lignin extraction, and this promising DES enable efficient pretreatment for economically feasible biomass conversion. This ChCl-BA DES facilitates environmentally friendly production of functional materials derived from cellulose and lignin under mild conditions.

Hydrothermal Liquefaction of Sugarcane Bagasse and Straw: Effect of Operational Conditions on Product Fractionation and Bio-Oil Composition

In the energy transition process, aiming for zero disposal and clean production in the elimination of waste is crucial; consequently, agricultural residues have significant potential for reduction in the use of fossil fuels. This study investigates the hydrothermal liquefaction (HTL) of sugarcane bagasse (BSC) and straw (SSC), examining the products’ distribution and bio-oil composition relative to the reaction conditions. The experiments used a 23 factorial design, evaluating the temperature (300–350 °C), constant heating time (0–30 min), and the use of the K2CO3 concentration as the catalyst (0–0.5 mol/L−1). The main factor affecting the biocrude yield from BSC and SSC was the use of K2CO3. Statistically significant interaction effects were also observed. Milder conditions resulted in the highest bio-oil yields, 36% for BSC and 31% for SSC. The catalyst had no impact on the biocrude production. The bio-oils were analyzed by GC/MS and FTIR; a principal component analysis (PCA) was performed to evaluate the samples’ variability. The FTIR highlighted bands associated with common oxygenated compounds in lignocellulosic biomass-derived bio-oils. The GC-MS results indicated a predominance of oxygenated compounds, and these were highest in the presence of the catalyst for both the BSC (90.6%) and SSC (91.7%) bio-oils. The SSC bio-oils presented higher oxygenated compound contents than the BSC bio-oils. Statistical analysis provided valuable insights for optimizing biomass conversion processes, such as determining the optimal conditions for maximizing product yields.

CO2 methanation: a bibliometric analysis and review of activated carbon-based materials (2014–24)

Abstract This study highlights the significant potential of activated carbon (AC)-based materials in environmental remediation and energy production, particularly in converting carbon dioxide (CO2) and hydrogen (H2) into methane (CH4) and water (H2O) using transition metal-based catalysts. It emphasizes the role of porous AC in waste reduction and resource utilization, examining various applications of CO2 and evaluating environmental impacts. The research explores commercialization opportunities and specifically investigates CO2 methanation using AC-based materials. Using bibliometric analyses of 4196 articles from the Web of Science database, the study identifies a growing research interest in porous AC-related CO2 methanation from 2014 to 2024. The top three journals in this field are Environment Development and Sustainability, Biomass Conversion and Biorefinery, and Journal of Environment Science and Pollution. However, there is limited inter-institutional collaboration in this field, suggesting room for development towards commercializing sustainable CH4 production pathways. CH4 is highlighted as a crucial intermediate in industrial processes, and research directions are identified through co-occurring author keywords analysis. The study suggests the need for a comprehensive approach integrating AC materials into carbon-neutral energy processes while addressing the potential adverse effects of AC nanoparticles on biological and environmental factors. Ultimately, it clarifies the potential uses and commercialization prospects for porous AC materials, especially in conjunction with carbon capture and utilization technologies, promoting sustainable practices in energy production and environmental management.

Effects of NaOH and Na2CO3 pretreatment on the saccharification of sweet sorghum bagasse

In this work, the chemical composition, chemical structures, and sugar release were evaluated for sweet sorghum bagasse (SSB) biomass in response to alkaline pretreatments and enzymatic hydrolysis. Five different ratios of 2 M sodium hydroxide (NaOH) and sodium carbonate (Na2CO3) solutions were used for biomass fractionation along with two heat treatment conditions, 85°C and 150°C for 1 h. Sugar yields from enzymatic hydrolysis were measured at different durations up to 72 h. SSB samples pretreated at high temperature using alkaline solutions containing equal amounts of Na2CO3 and NaOH favored retaining cellulose content (up to 90%) while effectively removing hemicellulose (65%) and lignin (92%). The high-temperature pretreatment conditions resulted in improved delignification, higher sugar concentrations, and sugar yields. Pretreatment solutions consisting of 50% or more NaOH produced higher glucose yields (85%–90%) and total sugar concentrations. Moreover, pretreatment solutions containing Na2CO3 improved the hydrolysis rates allowing SSB samples reach maximum yields faster than those without it, 48 versus 72 h. Results showed pretreatment methods combining NaOH and Na2CO3 were effective at promoting SSB biomass conversion, increasing sugar recovery after hydrolysis, and reducing the hydrolysis duration, all of which are desirable and cost beneficial.

A Thermogravimetric Analysis of Biomass Conversion to Biochar: Experimental and Kinetic Modeling

This study investigates the pyrolytic decomposition of apple and potato peel waste using thermogravimetric analysis (TGA). In addition, using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS), the influence of pyrolysis temperature on the physicochemical characteristics and structural properties of biochar was studied. The degradation of biomass samples was studied between 25 °C and 800 °C. Although apple and potato peel decomposition present similar thermogravimetric profiles, there are some differences that can be evidenced from DTG curves. Potato peel showed one degradation peak in the range 205–375 °C with 50% weight loss; meanwhile, the apple peel exhibited two stages: one with a maximum at around 220 °C and about 38% weight loss caused by degradation of simple carbohydrates and a second peak between 280 °C and 380 °C with a maximum at 330 °C, having a weight loss of approximately 24%, attributed to cellulose degradation. To gain more insight into the phenomena involved in biomass conversion, the kinetics of the reaction were analyzed using thermal data collected in non-isothermal conditions with a constant heating rate of 5, 10, 20, or 30 °C /min. The kinetic analysis for each decomposed biomass (apple and potato) was carried out based on single-step and multi-step type techniques by combining the Arrhenius form of the decomposition rate constant with the mass action law. The multi-step approaches provided further insight into the degradation mechanisms for the whole range of the decomposition temperatures. The effect of temperature on biomass waste structure showed that the surface morphologies and surface functional groups of both samples are influenced by the pyrolysis temperature. A higher pyrolysis temperature of 800 °C results in the disappearance of the bands characteristic of the hydroxyl, aliphatic, ether, and ester functional groups, characteristic of a porous surface with increased adsorption capacity. Therefore, this study concludes that biomass waste samples (apple and potato) can produce high yields of biochar and are a potential ecological basis for a sustainable approach. The preliminary adsorption tests show a reasonably good nitrate removal capacity for our biochar samples.

Thermal conversion of Achillea maritima biomass into dual-functional carbon quantum dots for antioxidant activity and methylene blue removal

Thermal conversion of Achillea maritima biomass into dual-functional carbon quantum dots for antioxidant activity and methylene blue removal

Membrane Separations in Biomass Processing.

The development of integrated biorefineries and the greater utilization of biomass resources to reduce dependence on fossil fuel-derived products require research emphasis not just on conversion strategies but also on improving separations associated with biorefining. A significant roadblock towards developing biorefineries is the lack of effective separation techniques evidenced by the lack of literature in this area. Additionally, high conversion yields may only be realized if effective separations generate feedstock of sufficient purity - this makes research into biomass conversion strategies all the more critical. In this review, the challenges associated with biomass separations are discussed, followed by an overview of the most appropriate separation strategies for processing biomass. One of the unit operations most appealing for biorefining, membrane separations (MS), is then considered along with a review of the recent literature utilizing this technique in biomass processing.

Niobium Pentoxide as an Acid Catalyst: An Overview

The global chemical industry is under increasing pressure to adopt more sustainable practices, as most chemical products exceed environmental safety limits. Given that chemical production largely relies on catalytic processes, the development of solid acid catalysts has become crucial for more sustainable production. Among these catalysts, niobium pentoxide stands out due to its strong acid sites, which remain active in the presence of water, and its stability under hydrothermal conditions. Recent studies have demonstrated that these solids maintain their catalytic activity even in the presence of strong bases, making them unique catalysts. This review explores the potential of niobium pentoxide as an acid catalyst, addressing advances in synthesis techniques, surface modifications, and combinations with other materials to enhance its catalytic performance in sustainable applications, such as biomass conversion and biofuel production, opening new pathways for the production of greener chemicals. Finally, the future perspectives of niobium pentoxide - based catalysts in green chemistry are discussed.

Biomass Demineralization and Pretreatment Strategies to Reduce Inhibitor Concentrations in Itaconic Acid Fermentation by Aspergillus terreus

Itaconic acid (IA) is a platform chemical, derived from non-petroleum sources, produced through the fermentation of glucose by Aspergillus terreus. However, producing IA from alternative sugar sources (e.g., lignocellulose) has been shown to be problematic, requiring post-hydrolysis mitigation to allow growth and IA production by the fungus. It is well known that the side products of lignocellulosic biomass conversion to sugars act as microbial growth inhibitors. An uncommon feature of fungal organic acid fermentations is production inhibition caused by mineral ions in biomass hydrolysate after pretreatment and enzymatic hydrolysis. To minimize mineral introduction during pretreatment and hydrolysis, we determined the sources of growth and production inhibitors at each of these steps. Biomass demineralization and four pretreatment strategies were evaluated for inhibitor introduction. Dilution assays determined the approximate degree of inhibition for each hydrolysate. An ammonium hydroxide pretreatment of demineralized wheat straw presented the lowest concentration of inhibitors and concomitant lowest inhibition: subsequent fermentations produced 35 g L−1 IA from wheat straw hydrolysate (91 g L−1 sugar) without post-hydrolysis mitigation.

One-pot catalytic conversion of cellulose biomass to bioethanol at low pressure and temperature conditions: H2O as a self-hydrolytic agent

One-pot catalytic conversion of cellulose biomass to bioethanol at low pressure and temperature conditions: H2O as a self-hydrolytic agent

Furfural production from xylan using a Pueraria Residues carbon-based solid-acid catalyst.

The conversion of biomass into high value-added platform compounds is an important method of biomass utilization. The conversion of hemicellulose represented by xylan into furfural can not only reduce the consumption of fossil fuels, but also promotes the development and utilization of non-edible biomass resources. In this study, a bifunctional solid-acid catalyst prepared from agricultural and forestry waste Pueraria (P. eduli) Residues was used to convert xylan into furfural in a biphasic system. In this study, P. eduli Residues was used as raw material to prepare a P. eduli Residues-based carbon solid-acid catalyst (PR/C-SO3H-Fe) by one-step sulfonation carbonization and impregnation. The catalyst catalyzes the conversion of xylan to furfural in a biphasic system (2-methyltetrahydrofuran/water). The physicochemical properties of the catalysts were characterized by X-ray powder diffraction, scanning electron microscopy, differential thermogravimetric analysis, Brunauer-Emmett-Teller surface area, Fourier transform infrared spectroscopy and ammonia temperature-programmed desorption. Subsequently, the experimental conditions were studied and optimized, such as metal species, iron ion concentration, reaction time and temperature, volume ratio of organic phase to water phase and ratio of substrate to catalyst. The results showed that under conditions of 160 °C, 50 mg catalyst, 100 mg xylan and 7 mL reaction solvent, the yield of furfural could reach 78.94% after 3 h of reaction. This study provides an effective research method for the conversion of xylan into furfural, and provides a reference for the catalytic conversion and utilization of hemicellulose in agricultural and forestry biomass. It also provides a feasible method for the resource utilization of agricultural and forestry waste. © 2024 Society of Chemical Industry.

A review on the heterogeneous catalyst for effective conversion of lignocellulosic biomass

This study examines a review of the heterogeneous catalyst for effective conversion of lignocellulosic biomass. In light of the challenges posed by a growing global population and the depletion of natural resources, there is an urgent need for alternative solutions. One such solution is the conversion of biomass into fuel, which has the potential to be a cost-effective and widely available substitute for fossil fuels. Solid catalysis and a range of chemical conversions effectively convert biomass into value-added chemicals. A critical factor in this process is the development of a highly efficient and selective catalysis system, along with the necessary chemical reactions. This review provides a comprehensive discussion of the various sources of biomass and their essential chemical composition. It also covers the conversion of biomass into a value-added chemical and the indispensable role of catalysis in the conversion process. Additionally, the review explores various conversion techniques for transforming biomass into useful forms of energy, and highlights their potential applications. By providing a detailed analysis of this process, this review aims to contribute constructively to the ongoing search for sustainable and effective solutions to energy challenges.

Fuel Quality from Thermochemical Conversion and Biological Treatment of Biomass

Fuel Quality from Thermochemical Conversion and Biological Treatment of Biomass

Comparison of pyrolysis and anaerobic digestion processes for wheat straw biomass

Due to the growing interest in using biomass as a renewable energy source, this study presents a comparative analysis between two prominent biomass conversion technologies—anaerobic digestion and biomass pyrolysis—focused on wheat straw biomass. The objective of this study is to evaluate and compare the efficiency, energy output, and environmental impact. Anaerobic digestion was performed under mesophilic conditions (35 ± 0.5 °C) using the biochemical methanogenic potential (BMP) methodology. Pyrolysis was conducted through thermogravimetric analysis (TGA) to determine the thermal behaviour and kinetic parameters of the biomass. Biogas production led to better energetic results as high methane yields of over 11 mL CH₄ g⁻¹ VS were obtained. Additionally, the integration of both processes was considered by subjecting digestate from anaerobic digestion to pyrolysis process. Key findings demonstrate that the activation energy (Ea) for wheat straw ranged from 166.49 to 176.42 kJ·mol−1 across different kinetic methods, indicating its suitability for pyrolysis. In contrast, digestates exhibited significantly lower activation energies, with 1-week, 2-weeks, and 3-weeks digestates showing ranges of 53.27–60.79 kJ·mol−1, 38.69–46.86 kJ·mol−1, and 46.29–72.34 kJ·mol−1, respectively. These results suggest that anaerobic digestion not only produces biogas but also yields a byproduct with potential for efficient pyrolytic conversion suggesting opportunities for integrated waste management and renewable energy production systems.

Operational optimization of a rural multi-energy system supported by a joint biomass-solid-waste-energy conversion system and supply chain

Biomass, as one of the most accessible renewable resources, could reduce dependency on fossil fuels and mitigate associated environmental impacts. With economic development and improved living standards, biomass in rural areas is converted into various forms of energy to meet high energy demands. However, existing studies on rural multi-energy system operations assume energy production from biomass is a given input parameter and consider it to be a fixed constant or subject to upper and lower bounds, independent of the biomass supply chain. Indeed, biomass energy production is significantly influenced by the collection, transportation, storage, and other processes within the supply chain. This work proposes a mixed integer linear program (MILP) for the joint optimization of an integrated rural multi-biomass-solid waste energy conversion system with a source-grid-demand-based biomass-solid waste supply chain (IRMBS-BSC system). The IRMBS-BSC system encompasses three sub-systems: the biomass-solid waste source sub-system, the biomass-solid waste grid sub-system, and the biomass-solid waste demand sub-system. Various biomass-solid wastes are classified, and a source model is established to evaluate their availability. Subsequently, a supply chain model is developed within the biomass-solid waste grid sub-system. Based on the available and transported quantity from the biomass-solid waste source sub-system and grid sub-system, a multi-energy system operation model, considering refined biomass conversion processes, is proposed. A case study involving a multi-energy system that integrates multiple rural community biomass-solid waste supplies is conducted. The results demonstrate that the proposed MILP, which considers the biomass-solid waste supply chain, can reduce energy imports during the load peak periods and can also decrease the overall operational costs of the multi-energy system.

Zirconium Phosphates and Phosphonates: Applications in Catalysis

This review covers recent advancements in the use of zirconium phosphates and phosphonates (ZrPs) as catalysts or catalyst supports for a variety of reactions, including biomass conversion, acid–base catalysis, hydrogenation, oxidation, and C-C coupling reactions, from 2015 to the present. The discussion emphasizes the intrinsic catalytic properties of ZrPs, focusing on how surface acidity, hydrophobic/hydrophilic balance, textural properties, and particle morphology influence their catalytic performance across various reactions. Additionally, this review thoroughly examines the use of ZrPs as supports for catalytic species, ranging from organometallic complexes and metal ions to noble metals and metal oxide nanoparticles. In these applications, ZrPs not only enhance the dispersion and stabilization of active catalytic species but also facilitate their recovery and reuse due to their robust immobilization on the solid support. This dual functionality underscores the importance of ZrPs in promoting efficient, selective, and sustainable catalytic processes, making them essential to the advancement of green chemistry.