Thermochemical Conversion Of Biomass Research Articles

Fuel Quality from Thermochemical Conversion and Biological Treatment of Biomass

Fuel Quality from Thermochemical Conversion and Biological Treatment of Biomass

A Review on Machine Learning-Aided Hydrothermal Liquefaction Based on Bibliometric Analysis

Hydrothermal liquefaction (HTL) is an effective biomass thermochemical conversion technology that can convert organic waste into energy products. However, the HTL process is influenced by various complex factors such as operating conditions, feedstock properties, and reaction pathways. Machine learning (ML) methods can utilize existing HTL data to develop accurate models for predicting product yields and properties, which can be used to optimize HTL operation conditions. This paper presents a bibliometric review on ML applications in HTL from 2020 to 2024. CiteSpace, VOSviewer, and Bibexcel were used to analyze seven key bibliometric attributes: annual publication output, author co-authorship networks, country co-authorship networks, co-citation of references, co-citation of journals, collaborating institutions, and keyword co-occurrence networks, as well as time zone maps and timelines, to identify the development of ML in HTL research. Through the detailed analysis of co-occurring keywords, this study aims to identify frontiers, research gaps, and development trends in the field of ML-aided HTL.

Towards Sustainable Biomass Conversion Technologies: A Review of Mathematical Modeling Approaches

The sustainable utilization of biomass, particularly troublesome waste biomass, has become one of the pathways to meet the urgent demand for providing energy safety and environmental protection. The variety of biomass hinders the design of energy devices and systems, which must be highly efficient and reliable. Along with the technological developments in this field, broad works have been carried out on the mathematical modeling of the processes to support design and optimization for decreasing the environmental impact of energy systems. This paper aims to provide an extensive review of the various approaches proposed in the field of the mathematical modeling of the thermochemical conversion of biomass. The general focus is on pyrolysis and gasification, which are considered among the most beneficial methods for waste biomass utilization. The thermal and flow issues accompanying fuel conversion, with the basic governing equations and closing relationships, are presented with regard to the micro- (single particle) and macro-scale (multi-particle) problems, including different approaches (Eulerian, Lagrangian, and mixed). The data-driven techniques utilizing artificial neural networks and machine learning, gaining increasing interest as complementary to the traditional models, are also presented. The impact of the complexity of the physicochemical processes and the upscaling problem on the variations in the modeling approaches are discussed. The advantages and limitations of the proposed models are indicated. Potential options for further development in this area are outlined. The study shows that efforts towards obtaining reliable predictions of process characteristics while preserving reasonable computational efficiency result in a variety of modeling methods. These contribute to advancing environmentally conscious energy solutions in line with the global sustainability goals.

Novel packed-bed CFD model for pellet combustion: Validation and application to a stove

An advanced CFD (computational fluid dynamics) model has been developed to describe the combustion of wood pellets. It is based on a packed-bed approach and provides a realistic description of the combustion of pellets, resolved in 3D over the whole fuel bed. It considers the properties of the packed bed rather than the properties of the single fuel particles. Compared to a particle-based description, simulation times are shorter due to the reduced complexity. In the model, the local conditions in different parts of the fuel bed (temperatures, flow conditions, oxygen concentrations …) influence the various stages of the combustion process (drying, pyrolysis, charcoal gasification and combustion). The compaction of the fuel bed due to shrinkage of the fuel particles during conversion and the loss of the particle structure shortly before the conversion is complete are also included in the description. The formulation of the bed compaction, the radiation absorption model and the charcoal conversion reactions have been specifically tuned to the combustion of wood pellets. The detailed pyrolysis model includes not only the main components, but also higher hydrocarbon species and tars in a manner specific to the fuel considered. It has been combined with a chemical gas phase mechanism which is a reduction of a detailed mechanism developed for thermo-chemical biomass conversion. The model has been validated against measurement data from a lab-scale batch reactor, and then applied to simulate the fuel bed of a commercial pellet stove. The simulation results are in good agreement with the corresponding measurements.

A novel molecular structure parameter determination method for biomass thermochemical conversion mechanism investigation

The low-grade energy properties and high O content of biomass limit its efficient energy utilization. Torrefaction is known to be one of the most promising thermochemical conversion methods for upgrading biomass. 250 °C Gas-pressurized (GP) torrefaction realizes deep decomposition of hemicellulose in biomass to as high as 99.7% by deoxygenation and aromatization. However, the above thermochemical conversion mechanism at molecular-level is currently scant. Here, a novel molecular structural parameter method and pure hemicellulose torrefaction were employed to investigate the thermochemical conversion mechanism. Results demonstrate that O content of 250 °C GP torrefied hemicellulose was as low as 28.8 wt%, which was considerably lower than 44.6 wt% of traditional torrefied hemicellulose. There are five deoxygenation mechanisms of hemicellulose during the GP torrefaction: deacetylation, decarbonylation, dehydroxylation, ring opening and cyclization reactions to produce CO2/CH3COOH, CO, H2O, ketones/aldehydes and furans. The deoxygenation and aromatization reactions cause the chemical structure of hemicellulose evolution significantly, these mechanisms are: active hemicellulose undergo aromatization reaction through cyclization and deoxidation to generate preliminary 2-ring furans polymer, followed by stepwise polymerization reactions to form 4-ring and 6-ring furans polymers. These polymerization reactions further greatly enhance deoxygenation reaction. A thermochemical conversion mechanism model is developed based on the above investigation. This work provides a novel method for determining the molecular structure and reaction mechanism of thermochemical converted biomass.

Performance of catalytic wet oxidation on thermochemical aqueous effluents assessed by FT-ICR MS

Aqueous phase (AP) is frequently observed in bio-oil from biomass thermochemical conversion or as an upgrading coproduct. However, AP contains high organic content that can be toxic and that must be reduced or removed to be then treated in existing wastewater plants. A promising method to upgrade these APs is the catalytic wet peroxide oxidation (CWPO) that was applied here on APs of both hydrothermal liquefaction and pyrolysis bio-oils from softwood and hardwood. Efficiency of the CWPO was assessed by investigating the molecular composition of raw and treated APs by ultra-high-resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) with electrospray ionization (ESI) in negative- and positive-ion modes. Combination of FT-ICR MS and multivariate statistical analyses evidenced efficiency of the process with new compounds resulting from the oxidative depolymerization, characterized by lower unsaturation degree and molecular weight, and higher oxygen atom count. Refractory compounds were also observed, which are notably characterized by high unsaturation degrees. Interestingly, both detection modes were shown to be complementary for the understanding of the CWPO process. ESI (-) allowed to assess the completion of the oxidation process in detecting carboxylic acid conversion products and to specifically evidence refractory products. ESI (+) was informative on the CWPO process, especially on the conversion of the basic compounds, with the decrease of the detected species. Eventually, softwood AP was shown to be more reluctant to CWPO than the hardwood one.

Progress in the preparation of biomass energy from steam-exploded lignocellulose

Steam explosion is an effective pretreatment method for the thermochemical conversion of biomass and an efficient way to produce sugars and fuels from lignocellulose. It breaks down the recalcitrant and complex structures in biomass, which are then converted into substances such as methane and fermentable sugars, and has great potential to mitigate global oil depletion and the threat of climate change. This review evaluates the effect of steam explosion temperature, dimension pressure time, and additive type factors on the pretreatment effect of the steam explosion method. The changes in the content and physical structure of the components in the treated biomass are also explored. The advantages and disadvantages of this means for the subsequent process and its application in industrial production are analyzed in depth to provide technical reference for steam explosion in the preparation of biomass from lignocellulose.

Multi-objective optimization of a dual fuel CI engine powered with syngas and pilot diesel using TLBO algorithm: A metaheuristic approach

Abstract The thermochemical conversion of biomass into producer gas presents an attractive alternative fuel option for compression ignition (CI) engines, making biomass gasification a critical driver for achieving sustainable development goals. Considering the application of producer gas (PG) in CI engine, the most potential gases include H2 and CO as main fuel compounds and it is crucial to comprehensively understand the impact of these two gas components on the engine behaviour. Nowadays, artificial intelligence-powered models are frequently applied for simulating engines that run on a single type of fuel. However, their usage is not as common when it comes to modeling dual-fuel CI engines run on synthetic producer gas or syngas. The present study explores the feasibility of optimizing operational parameters, such as engine load and syngas composition, in improving the efficiency and lowering the levels of pollutants emitted by a 3.5 kW CI engine operated under dual fuel (DF) mode using syngas as primary fuel and diesel as pilot fuel. The performance and emission characteristics of syngas (H2:CO) is examined by studying its behaviour in four different combinations. The compositions of syngas are prepared based on the volumetric percentage of the H2 and CO and is inducted into the combustion chamber using a novel venturi-type air-gas mixer. In the present study, an intelligent metaheuristics-based optimization algorithm i.e., Teaching–Learning Based Optimization (TLBO) is developed and introduced, to develop a predictive model within constrained range of engine operating conditions. Further, the algorithm is used to estimate multiple engine performance characteristics simultaneously viz., brake thermal efficiency (BTE), unburned hydrocarbons (HC), and carbon monoxide (CO). The resultant findings identify the optimal engine load of 68.87% and the ideal syngas composition of 63.9% H2 and 49.5% CO as key parameters for maximizing engine efficiency while minimizing exhaust emission. At these optimized operating condition, 19.49% BTE is observed, while HC and CO emission was found to be 384.6 ppm and 445.33 ppm respectively. This shows the effective and efficiency of the proposed algorithm.

Theoretical Study on the Pyrolysis Mechanism of the Lignin Dimer Model Compound Catalyzed by Alkaline Earth Metal Ions Ca2+ and Mg2+

It is essential to investigate the influence of alkaline earth metals on the pyrolysis mechanism and resulting products of lignin to enhance the efficient thermochemical conversion and utilization of lignin or biomass. In this study, the density functional theory method was used to simulate the pyrolytic reaction pathways of a β-O-4 type lignin dimer model compound (1-methoxy-2-(4-methoxyphenethoxy)benzene, mc) affected by alkaline earth metal ions Ca2+ and Mg2+. The computational findings suggest that Ca2+ and Mg2+ tend to combine with the oxygen atom at the Cβ position and the oxygen atom on the methoxy group of the lignin dimer model compound, forming stable complexes that modify the bond lengths of the Cα–Cβ and Cβ–O bonds and affect their pyrolysis energy barriers. During the catalytic pyrolysis process, the presence of Ca2+ and Mg2+ can promote the concerted decomposition reaction, leading to increased production of products like 1-methoxy-4-vinylbenzene, 2-methoxyphenol and catechol. Meanwhile, they can suppress homolytic cleavage reactions of the Cβ–O and Cα–Cβ bonds, thereby hindering the formation of other products such as 1-ethyl-4-methoxybenzene and 2-hydroxybenzaldehyde.

Hydrochar from winemaking industry wastes as solid biofuel: A thermal and kinetic analysis of pyrolysis and combustion

Pyrolysis and combustion behavior of the hydrochar (HY) from co-hydrothermal carbonization (co-HTC) of vine pruning (VP) and exhausted grape marc (EGM) by using vinasse as wet catalytic vector was investigated through thermogravimetric analysis (TGA). For both raw- and co-HTC biomass, different iso-conversional methods were used for kinetic analysis, and the thermodynamic parameters were determined. Overall, even if HY exhibited a lower activation energy compared to EGM and VP during both pyrolysis and combustion, HTC has positive effects on the hydrochar’s structure, which achieved a more thermodynamically stable, structurally ordered, and energetically favorable state. The obtained kinetic and thermodynamic parameters would contribute to the development of biomass thermochemical conversion technologies and the application of hydrochar-based energy systems.

Efficient Glucose Isomerization to Fructose using Photoregenerable MgSnO3 Catalyst with Cooperative Acid-Base Sites.

The isomerization of glucose to fructose plays a crucial role in the food industry and the production of biomass-derived chemicals in biorefineries. However, the catalyst used in this reaction suffers from low selectivity and catalyst deactivation due to carbon or by-product deposition. In this study, MgSnO3 catalyst, synthesized via a facile two-step process involving hydrothermal treatment and calcination, was used for glucose isomerization to fructose. The catalyst demonstrated outstanding catalytic performance, achieving a fructose equilibrium yield of 29.8 % with a selectivity exceeding 90 % under mild conditions owing to its acid-base interaction. Notably, spent catalysts can be regenerated by photoirradiation to remove surface carbon, thereby avoiding the changes in properties and subsequent loss of activity associated with conventional calcination regeneration method. This novel approach eliminates the energy consumption and potential structural aggregation associated with traditional calcination regeneration methods. The acid-base active sites of the catalyst, along with their corresponding catalytic reaction mechanism and photoregeneration mechanism were investigated. This study presents a demonstration of the comprehensive utilization of catalytic material properties, i. e., acid-base and photocatalytic functionalities, for the development of a green and sustainable biomass thermochemical conversion system.

Thermochemical conversion of oil palm biomass and its applications: A bibliometric exploration of global trends over two decades

In the context of rising global palm oil production and increasing focus on renewable energy, this bibliometric analysis explores literature trends and the impact of scholarly articles on the thermochemical conversion of oil palm biomass (OPB). Data from 2004 to 2023, sourced from Scopus, was validated and analyzed using Microsoft Excel and VOSViewer. The search yielded 2215 articles after multiple phases of collecting and refining textual content from Scopus. The analysis maps out research frontiers, themes, and connections, including combustion, gasification, pyrolysis, torrefaction, and liquefaction. Malaysia emerged as the leading country in terms of research output. In terms of technologies, pyrolysis was the most researched technology. The analysis was further deepened to include specific application-related subtopics, focusing on keywords such as diesel, biofuel, adsorption, supercapacitor, phenol, and hydrogen production, which show significant linkage and occurrence in author keyword searches. This study provides a comprehensive overview of the research landscape in this field, highlighting crucial areas for future exploration.

Atlas of Microscopic Images of Biochar

Derived through the thermochemical conversion of biomass, biochar is a carbon-rich substance recognized for its significance in environmental applications and sustainable agriculture. As interest in its utilization continues to rise, it becomes crucial to comprehend how the source material and pyrolysis parameters influence the properties of biochar and, consequently, to research the suitability of various analytical methods for characterizing it. Despite the current utilization of numerous physical and chemical methods, the untapped potential of reflected light microscopy warrants further exploration. While a few recent studies suggest a correlation between certain microscopic characteristics and selected physical and chemical properties of biochar, the data are limited and difficult to compare. This is primarily due to variations in the types of original biomass used and lack of information about pyrolysis conditions. Moreover, because only a limited number of photographs taken under a reflected light microscope are publicly available to-date, it is difficult to evaluate morphological differences between various biochars and other organic materials such as inertinites from coal, charcoal, etc. To address limited availability of publicly available data, this “Atlas of Microscopic Images of Biochar” presents a collection of more than 300 images contributed by researchers from Poland, the United States, Canada, Australia, Brazil, and Denmark. These photomicrographs capture optical characteristics of a diverse array of biochar, demonstrating its unique morphological and structural features. This visual documentation can serve as a valuable resource for researchers, industry professionals, educators, and enthusiasts interested in investigating the complexities of biochar forms.

Tailoring microwave frequencies for high-efficiency hydrogen production from biomass

Generating green hydrogen through biomass thermochemical conversion is pivotal for contributing to carbon neutrality. However, the efficiency of hydrogen production is hindered by the byproduct of tar formed during biomass depolymerization. This study employed a variable-frequency microwave ranging from 2430 to 6000 MHz to investigate the influence of microwave frequency on tar removal and hydrogen recovery over activated charcoal (AC). Experimental results indicated that microwave frequencies significantly impact the temperature distribution and heating rates of AC. Notably, at 4640 MHz the AC rapidly reached 1145 °C within seconds, with an instantaneous heating rate of 2022 °C/min. The ultra-fast heating rate crucially contributes to achieving 100 % efficiency in tar cracking, resulting in a hydrogen yield of 32.8 mmol/g. With a hydrogen recovery rate surpassing 94 %, the 4640 MHz frequency represents a 15.4-fold increase compared to the conventional 2450 MHz. This innovative approach holds significant promise for enhancing energy efficiency in the pursuit of carbon-neutral energy production.

Review of Methods for Converting Biomass into Biofuels

Thermochemical processes are among the most effective methods of obtaining hydrogen-rich gases from biomass. These technologies mainly include pyrolysis, gasification and hydrothermal liquefaction. Thermochemical conversion of dry biomass is similar to the conversion of fossil fuels using gasification and pyrolysis methods. Products obtained through thermochemical processes (CO and CH4) can be processed into other biofuels, e.g. syngas, a raw material for producing synthetic hydrocarbons, methanol and alcohols. In recent years, advanced research has been carried out using biomass to produce liquid fuels. The biomass pyrolysis process in the presence of a catalyst is based on the rapid heating of the biomass to a temperature of approximately 500°C in the so-called inert atmosphere in which there are no reactive gases. This process produces a liquid product: pyrolysis oil, gas and charcoal. The bio-oil produced in this process constitutes 60-75% of the mass of the biofuel and is thermally unstable because it contains up to 300 different chemical compounds. However, the bio-oil obtained in this way is incompatible with conventional liquid transport fuels (gasoline, diesel) due to its high oxygen content. Pyrolysis in the presence of a zeolite catalyst is a process that allows for the effective conversion of biomass in economic and ecological terms. A zeolite catalyst makes it possible to remove oxidized compounds in situ and modify the properties of the biofuel to ensure its compatibility with conventional transport fuels. The catalyst plays a crucial role in this process because it removes oxygen from oxygenates and, consequently, creates stable reaction products that can then be treated to obtain renewable transport fuels or other useful chemicals. The article presents methods of biomass conversion via pyrolisis, microorganisms usage, zeolite-based catalysis, biocatalysis and photo-fermentation, which poses a big possibility of diversification of renewable energy sources.

Remediation of mine overburden and contaminated water with activated biochar derived from low-value biowaste

BackgroundMines can be regarded as the economic backbone of India with a contribution of 10–12 % towards the gross domestic production with industrial demand. It gives rise to environmental problems like soil, water and air pollution. The active mines generate lots of waste rock and wastewater that contaminate nearby soil and water bodies with heavy metals. MethodsThe elimination of heavy metals by suitable amendments is emerging as a potential solution to such problems. Biochar, a carbon rich, stable, alkaline and porous product of thermo-chemical conversion of biomass has emerged as a promising adsorbent of heavy metals. Conversion of these biowastes into biochar is a sustainable approach as it fulfills multiple objectives of waste utilization, and pollution abatement. Significant findingsDue to its large surface area, biochar can restrain heavy metals while modified biochar has an increased potential for adsorption with an increased surface area. The review emphasizes the type of mines, overburden generation, their impact on soil and water, and the utility of different biowastes available to be mobilized into biochar for remediation of contaminated water and soil. It also bridges the gap in the current knowledge on the activation techniques of biochar with heavy metals remediation.

Kinetic and quantitative analysis of gaseous products of thermochemical biomass conversion based on thermogravimetric and mass‐spectrometric data

AbstractThe aim of this study is to apply a new approach to the quantitative analysis of the formation of gaseous products generated during the thermochemical conversion of wood waste samples of different fineness by using thermogravimetric analysis with mass spectrometry (TGA‐MS). Profiles of the release of gaseous components in the process of thermochemical conversion of wood samples were obtained based on data from the combined use of mass spectrometry and thermogravimetry. The resulting mass spectrometric data were processed according to the proposed methodology and the characteristics of the released gases were noted. The kinetic coefficients of the gases’ formation were calculated from the processed data.

Impact of high-temperature biomass pyrolysis on biochar formation and composition

The development and utilization of biomass play a vital role in reducing fossil fuel dependency and mitigating greenhouse gas emissions. High-temperature pyrolysis provides a promising route for converting biomass into valuable products without tar formation. Kinetic models are essential for understanding biomass pyrolysis processes, aiding reactor design and optimization. In this study, rice husk (RH) and corn straw (CS) are selected, which exhibit significant differences in ash content but are widely present. Pyrolysis is performed using a thermogravimetric analyzer coupled with a mass spectrometer (TGA-MS). The results show a rapid decrease in solid residue oxygen content at elevated temperatures, which stabilized after reaching 900°C, accounting for about 8–10%. MS quantification indicates increased release of H2O and CO during this stage. Fourier transform infrared spectroscopy (FTIR) analysis on the biochar unveils that this phenomenon is attributed to the stretching vibration of C-O bonds and the conversion of -OH groups. The remaining oxygen primarily exists as carbonyl and carboxyl groups. Subsequently, the CRECK-S-B biomass pyrolysis kinetic model is updated, specifically targeting the transformation mechanism of oxygen-containing solids at high temperatures to improve the prediction of biochar yield and elemental composition. The relative error of oxygen content prediction is less than 10%. The accuracy of the model is validated through experimental data and an extensive literature database, leading to the establishment of a comprehensive database. The updated model demonstrates significantly enhanced prediction accuracy for pyrolysis temperatures above 800°C, expanding its applicability range. Moreover, it achieves an accuracy rate exceeding 80% for char yield and elemental content in the temperature range of 200–1000°C, including torrefaction conditions. It provides a theoretical foundation for the effective utilization of high-temperature biochar, offers a novel insight into biomass thermochemical conversion, and contributes to the sustainable development of biomass energy.

Coupling coarse‐grained DEM‐CFD and intraparticle model for biomass fast pyrolysis simulation and experiment validation

AbstractThe understanding of complex fluidization hydrodynamics and chemical reactions in biomass fast pyrolysis fluidized bed reactors is lacking and requires further investigation. It is urgent to develop accurate mathematical models capable of describing the complex multiphase reaction system of biomass pyrolysis. A comprehensive multiscale model based on coarse‐grained discrete element method (DEM)‐computational fluid dynamics (CFD) was developed in open‐source MFiX code. It incorporates detailed biomass pyrolysis kinetics and an intraparticle model. To validate the model, measurements were conducted in a fluidized bed pyrolyzer, including quantifying the segmental pressure drop along the height of the bed and determining the yields and compositions of gas, liquid, and solid products. The particle mixing and segregation, axial distribution and residence time, Lacey index, and pyrolysis products were investigated. The study provides experimental and theoretical foundations for designing multiphase fluidized bed reactors and advancing biomass thermochemical conversion.

Assessment and modeling of mercury adsorption on carbon-based adsorbents prepared from Jacaranda mimosifolia and guava biomass via pyrolysis and hydrothermal carbonization

Abstract The mercury adsorption properties of carbon-based materials prepared from jacaranda (Jacaranda mimosifolia) and guava (Psidium guajava) seed wastes are reported and compared in this paper. These adsorbent samples were obtained via pyrolysis and hydrothermal carbonization. Mercury adsorption equilibrium was studied at pH 4 and 20–40 °C, and the adsorption enthalpy changes were calculated for all adsorbent samples. The results showed that jacaranda-based materials contained a higher amount of acidic functional groups than guava seed-based adsorbents, and consequently, their mercury adsorption properties were better. The surface area of these adsorbents was <10 m2/g thus being classified as low-porosity materials. Elemental analysis indicated that all adsorbents were mainly composed of oxygen (4–25%) and carbon (75–95%). The calculated adsorption capacities at saturation of the best adsorbent were 18.05–30.09 mg/g under the tested experimental conditions. Statistical physics calculations also indicated that the adsorption mechanism of HgCl2 species was multi-molecular and endothermic. Ligand exchange and van der Waals forces were involved in generating the mercury–adsorbent interface. These results highlight the importance of comparing and optimizing biomass thermochemical conversion routes to tailor the surface properties of adsorbents used for water purification.