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Catalytic esterification of acid-rich coffee waste-derived bio-oil was performed using sulfonated metal oxide catalysts (Al2O3, MgO, ZrO2, and TiO2) and ethanol to produce fatty acid alkyl esters. The potential of the sulfonated catalysts for esterification decreased in the following order: Ti-SO4 > Zr-SO4 > Al-SO4 > Mg-SO4. Particularly, Ti-SO4 and Zr-SO4 resulted in 91.2 % (peak area %) and 85.2 % esters, respectively. This is attributed to the contributions of well-dispersed Brønsted acid sites created by -SO3H functional groups, additional Lewis acid sites formed by Ti and Zr oxides, and their appropriate pore size. Compared with HCl and H3PO4, the use of H2SO4 for TiO2 treatment significantly enhanced ester formation. When using Ti-SO4, increasing the catalyst-to-feedstock ratio (1/2 â¼ 1/10) significantly increased the esters' selectivity (38.7 %â¼94.7 %). Ethanol utilization caused a superior selectivity for esters than methanol, while the increasing temperature favored ester production. This study proposes an eco-friendly and practical method for biodiesel generation.
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Biocombustíveis , Café , Esterificação , Catálise , Café/química , Ácidos Sulfônicos/química , Resíduos , Ésteres/química , Óleos de Plantas/química , PolifenóisRESUMO
Solar-driven artificial photosynthesis offers a promising avenue for hydrogen peroxide (H2O2) generation, an efficient and economical replacement for current methods. The efficiency and selectivity hurdles of the two-electron oxygen reduction reaction (ORR) in solar-to- H2O2 conversion are substantial barriers to large scale production. In this manuscript, a simple biomass-assisted synthesis was performed to produce oxygen-enriched carbon quantum dots (OE-CQDs) from spent coffee waste, acting as an efficient photocatalyst for solar-powered H2O2 production. OE-CQDs can stabilize and store light-generated electrons effectively, boosting charge separation and enhancing photocatalytic performance with longevity. The maximal photocatalytic H2O2 production was achieved viz the utilization of OE-CQDs with generation rate of 356.86 µmol g-1 h-1 by retaining 80% activity without any external sacrificial donors. The outstanding performance of synthesized OE-CQDs under light exposure at wavelength (λ) of 280 nm has been ensured by the quantum yield value of 9.4% upon H2O2 generation. The combinatorial benefits of OE-CQDs with their authentic crystalline structure and oxygen enrichment, is expected to be enhancing the ORR activity through accelerating charge transfer, and optimizing oxygen diffusion. Consequently, our eco-friendly method holds considerable promise for creating highly efficient, metal-free photocatalysts for artificial H2O2 production.
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Carbono , Café , Peróxido de Hidrogênio , Oxigênio , Pontos Quânticos , Luz Solar , Pontos Quânticos/química , Oxigênio/química , Catálise , Peróxido de Hidrogênio/química , Carbono/química , Café/química , Oxirredução , Processos FotoquímicosRESUMO
The use of lignocellulosic waste as an energy source for substituting fossil fuels has attracted lots of attention, and pyrolysis has been established as an effective technology for this purpose. However, the utilization of bio-oil derived from non-catalytic pyrolysis faces certain constraints, making it impractical for direct application in advanced sectors. This study has focused on overcoming these challenges by employing fractional condensation of pyrolytic vapors at distinct temperatures. The potential of five types of sawdust for producing high-quality bio-oil through pyrolysis conducted with a bench-scale bubbling fluidized bed reactor was investigated for the first time. The highest yield of bio-oil (61.94 wt%) was produced using sample 3 (damaged timber). Remarkably, phenolic compounds were majorly gathered in the 1st and 2nd condensers at temperatures of 200 °C and 150 °C, respectively, attributing to their higher boiling points. Whereas, carboxylic acid, ketones, and furans were mainly collected in the 3rd (-5 °C) and 4th (-20 °C) condensers, having high water content in the range of 35.33%-65.09%. The separation of acidic nature compounds such as acetic acid in the 3rd and 4th was evidenced by its low pH in the range of 4-5, while the pH of liquid collected in the 1st and 2nd condensers exhibited higher pH (6-7). The well-separated bio-oil derived from biomass pyrolysis facilitates its wide usage in various applications, proposing a unique approach toward carbon neutrality. In particular, achieving efficient separation of phenolic compounds in bio-oil is important, as these compounds can undergo further upgrading to generate hydrocarbons and diesel fuel.
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Temperatura Alta , Polifenóis , Pirólise , Biocombustíveis , Óleos de Plantas , Fenóis/análise , BiomassaRESUMO
Electrode-driven microbial electron transfer enables the conversion of CO2 into multi-carbon compounds. The electrosynthetic biofilms grow slowly on the surface and are highly susceptible to operational influences, such as hydrodynamic shear stress. In this study, a cylindrical roll-up carbon felt electrode was developed as a novel strategy to protect biofilms from shear stress within the reactor. The fabricated electrode allowed hydrogen bubble formation inside the structure, which enabled microbes to uptake hydrogen and convert CO2 to multi-carbon organic compounds. The roll-up electrode exhibited faster start-up and biofilm formation than the conventional linear shape carbon felt. The acetate yield and cathodic faradaic efficiency increased by 80% and 34%, respectively, and the bioelectrochemical stability was improved significantly. The roll-up structure increased biofilm development per unit electrode surface by three to five-fold. The roll-up configuration improved biofilm formation on the electrode, which enhanced the performance of microbial electrosynthesis-based CO2 valorization.
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Dióxido de Carbono , Carbono , Dióxido de Carbono/química , Habitação , Fibra de Carbono , Hidrogênio , Eletrodos , BiofilmesRESUMO
Wax is a detrimental byproduct of plastic waste pyrolysis causing challenges upon its release into the environment owing to persistence and potential toxicity. In this study, the valorization of wax materials through conversion into BTEX (i.e., benzene, toluene, ethylbenzene, and xylene) was achieved via catalytic pyrolysis using zeolite-based catalysts. The potential of two types of waxes, spent wax (SW), derived from the pyrolysis of plastic waste, and commercial paraffin wax (PW), for BTEX generation, was investigated. Using HZSM-5, higher yields of oil (54.9 wt%) and BTEX (18.2 wt%) were produced from the pyrolysis of SW compared to PW (32.3 and 14.1 wt%, respectively). This is due to the improved accessibility of lighter hydrocarbons in SW to Brønsted and Lewis acid sites in HZSM-5 micropores, promoting cracking, isomerization, cyclization, Diels-Alder, and dehydrogenation reactions. Further, the use of HZSM-5 resulted in significantly larger yields of oil and BTEX from SW pyrolysis compared to Hbeta and HY. This phenomenon is ascribed to the well-balanced distribution of Brønsted and Lewis acid sites and the identical geometric structure of HZSM-5 micropores and BTEX molecules. The addition of Ga to HZSM-5 further led to 2.24% and 28.30% enhancements in oil and BTEX yields, respectively, by adjusting the acidity of the catalyst through the introduction of new Lewis acid sites. The regeneration of the Ga/HZSM-5 catalyst by removing deposited coke on the spent catalyst under air partially recovered catalytic activity. This study not only offers an efficient transformation of undesirable wax into valuable fuels but also provides an environmentally promising solution, mitigating pollution, contributing to carbon capture, and promoting a healthier and more sustainable environment. It also suggests future research directions, including catalyst optimization and deactivation management, feedstock variability exploration, and techno-economic analyses for sustainable wax conversion into BTEX via catalytic pyrolysis.
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Ácidos de Lewis , Pirólise , Hidrocarbonetos , Tolueno , Catálise , Meio Ambiente , Temperatura AltaRESUMO
Using renewable photocatalysts for pollutant degradation represents a promising approach to addressing environmental water challenges by harnessing solar energy without additional energy consumption. However, for the practical use of photocatalysts, it is necessary to improve catalyst efficiency, considering cost and biocompatibility. In this study, we developed a new superabsorbent photocatalyst for the degradation of organic dyes in water. Our photocatalyst comprises halloysite nanotubes (HNTs) with a large outer diameter and Si-O and Al-O groups on the outer and inner surfaces, respectively; graphene oxide (GO) possessing numerous sp2 bonds and light-conductive properties; and ZnO, which can degrade organic molecules via a photon source. By exploiting the superabsorbent properties of GOs for organic dyes and stabilizing ZnO nanoparticles on HNTs to inhibit aggregation, our photocatalysts demonstrated significantly improved degradability compared to ZnO nanoparticles alone and combinations of ZnO with HNTs or GO. The structural characteristics of the nanocomposites were characterized using SEM, EDX, Raman spectroscopy, and XRD. Their enhanced photocatalytic activity was demonstrated by the degradation of rhodamine b in water, showing 95% photodegradation under UV illumination for 60 min, while the ZnO nanoparticles showed only 56% dye degradation under the same condition. Additionally, the degradation rate was enhanced by four times. Furthermore, the catalysts maintained their initial activity with no significant loss after four uses, showing their potential for practical implementation in the mass purification of wastewater.
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The efficient hydrolysis of cellulose into its monomer unit such as glucose or valuable cello-oligosaccharides is the critical step for the cost-effective production of biofuels and biochemicals. However, the current cellulose hydrolysis process involves high energy-demanding pretreatment (e.g., ball-milling) and long reaction times (>24 h). Herein, we investigated the feasibility of the dissolution/regeneration (DR) of cellulose in ionic liquids (ILs) and deep eutectic solvent (DES) as an alternative to ball-milling pretreatment for the effective hydrolysis of cellulose. Because chlorine-based solvents were reported to be the most active for cellulose pretreatment, [EMIM]Cl and [DMIM]DMP were selected as the IL molecules, and choline chloride-lactic acid and choline chloride-imidazole were selected as the DES molecules. The level of the crystallinity reduction of the regenerated cellulose were analyzed using XRD and SEM measurements. The hydrolysis kinetics of the regenerated cellulose from ILs and DES were examined at 150 °C using sulfonated carbon catalysts and compared with those of the ball-milled cellulose. Overall, the cellulose pretreatment using the ILs and the DES had superior kinetics for cellulose hydrolysis to the conventional ball milling treatment, suggesting a possibility to replace the current high energy-demanding ball-milling process with the energy-saving DR process. In addition, the utilization of supercritical carbon dioxide-induced carbonic acid as an in situ acid catalyst for the enhanced hydrolysis of cellulose was presented for the first time.
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The interactions between the microbes and the surface of an anode play an important role in capturing the respiratory electrons from bacteria in a microbial fuel cell (MFC). The chemical and electrochemical characteristics of the carbon material affect biofilm growth and direct electron transfer in MFCs. This study examined the electrodeposition of polydopamine (PDA) and polypyrrole (PPY) on graphite felt electrode (GF). The MFC with the modified PDA/PPY-GF reached 920 mW/m2, which was 1.5, 1.17, and 1.18 times higher than those of the GF, PDA-GF, and PPY-GF, respectively. PDA has superior hydrophilicity and adhesive force biofilm formation, while PPY provides electrochemically active sites for microbial electron transfer. Raman spectroscopy, Fourier transform infrared spectroscopy, Brunauer-Emmett-Teller surface area measurements, and contact angle analysis revealed the enhanced physicochemical properties of the carbon electrode. These results show that co-doped PDA/PPY provides a strategy for electroactive biofilm development and improves the bioelectrochemical performance in realistic MFC reactors.
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Fontes de Energia Bioelétrica , Grafite , Fontes de Energia Bioelétrica/microbiologia , Polímeros/química , Grafite/química , Pirróis/química , Bactérias , Carbono , EletrodosRESUMO
Renewable electricity-based microbial electrosynthesis can upgrade CO2 into value-added chemicals and simultaneously increase the number of biocatalysts by cell growth, helping to achieve sustainable carbon-negative processes. In most studies, the main strategy for improving the MES performance was to enhance H2-based electron uptake by decreasing the overpotential and electrical conductivity of the electrode. Less is known about the electrode-based direct electron uptake for CO2 conversion in MES. In this study, a solid neutral red/Nafion conductive layer was developed on the carbon electrode surface using a feasible dip and dry method. The modified electrode showed higher HER overpotential and lower capacitance but enhanced redox capability and hydrophobicity, which increased direct electron transport to the bacteria rather than hydrogen-based indirect electron delivery. The Neutral red/Nafion-implemented MES showed faster start-up, higher acetate production, and energy efficiency than the non-modified electrode.
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Dióxido de Carbono , Carbono , Acetatos/metabolismo , Dióxido de Carbono/metabolismo , Fibra de Carbono , Conservação de Recursos Energéticos , Condutividade Elétrica , Eletrodos , Polímeros de Fluorcarboneto , Hidrogênio , Vermelho NeutroRESUMO
The aim of this work was to study on MgO-modified KOH activated biochar (AC) catalysts, in the pyrolysis of sawdust for the direct production of bio-jet fuels using a tandem micro-pyrolyzer. AC catalysts with various MgO contents (5 to 20â¯wt%) were synthesized using an impregnation method. The mesopores generated (4 to 18â¯nm) in the carbon has a great potential in the conversion of oxygenated to jet fuel. The importance of basic nature in the catalysts is demonstrated with the maximum bio-jet fuel yield of 29 % at 10 % MgO. Further, the temperature of 600⯰C and a catalyst/sawdust ratio of 10 are identified as the optimal conditions. The nanosize of MgO and the synergism of acid and base sites seemed to enhance deoxygenation, via decarboxylation and decarbonylation, and oligomerization, which are required for jet fuel formation in high amounts from sawdust pyrolysis.
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Óxido de Magnésio , Pirólise , Biocombustíveis , Carvão Vegetal , Temperatura AltaRESUMO
In this study, wasted mask is chosen as a pyrolysis feedstock whose generation has incredibly increased these days due to COVID-19. We suggest a way to produce value-added chemicals (e.g., aromatic compounds) from the mask with high amounts through catalytic fast pyrolysis (CFP). To this end, the effects of zeolite catalyst properties on the upgradation efficiency of pyrolytic products produced from pyrolysis of wasted mask were investigated. The compositions and yields of pyrolytic gases and oils were characterized as functions of pyrolysis temperature and the type of zeolite catalyst (HBeta, HY, and HZSM-5), including the mesoporous catalyst of Al-MCM-41. The mask was pyrolyzed in a fixed bed reactor, and the pyrolysis gases evolved in the reactor was routed to a secondary reactor inside which the zeolite catalyst was loaded. It was chosen 550 °C as the CFP temperature to compare the catalyst performance for the production of benzene, toluene, ethylbenzene, and xylene (BTEX) because this temperature gave the highest oil yield (80.7 wt%) during the non-catalytic pyrolysis process. The large pore zeolite group of HBeta and HY led to 134% and 67% higher BTEX concentrations than HZSM-5, respectively, likely because they had larger pores, higher surface areas, and higher acid site density than the HZSM-5. This is the first report of the effect of zeolite characteristics on BTEX production via CFP.
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COVID-19 , Zeolitas , Catálise , Temperatura Alta , Humanos , Pirólise , SARS-CoV-2RESUMO
Hydrogenation of biomass-derived furfural is an important process in biofuel production. Herein, different Pt-supported TiO2 morphologies: nanorod (NR), nanoparticle (NP), and hollow microsphere (HMS) were prepared by the impregnation-chemical reduction method. The furfural conversion increased with an increase of Pt dispersion. However, cyclopentanone selectivity was affected by TiO2 properties, the strong metal-support interaction (SMSI) effect, and the reaction conditions. The Pt/TiO2 NR catalyst exhibited the highest cyclopentanone selectivity of 50.4%. Based on the H2-temperature programmed desorption (H2-TPD) and X-ray photoelectron spectroscopy (XPS) results, the Pt/TiO2 NR catalyst showed a SMSI effect, which was introduced by the chemical reduction method. We suggest that electron charge transfer from Ti species to Pt in the Pt/TiO2 NR catalyst affects the cyclopentanone selectivity by controlling the adsorption strength between the reactant and the Pt surface, thus retarding the formation of byproducts.
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This work investigated the impact of pyrolysis medium and catalyst on the production of bio-BTX (benzene, toluene, and xylene) from Quercus Mongolica (Q. Mongolica) via catalytic pyrolysis. Two different pyrolysis media (N2 and CH4) and five different zeolite catalysts (HY, HBeta, HZSM-5, 1 wt% Ni/HZSM-5, and 1 wt% Ga/HZSM-5) were considered for the Q. Mongolica pyrolysis. The HZSM-5 yielded more BTX than the HY and HBeta due to its strong acidity. The employment of CH4 as the pyrolysis medium improved the BTX yield (e.g., 2.7 times higher total BTX yield in CH4 than in N2) and resulted in low coke yield (e.g., 5.27% for N2-pyrolysis and 2.57% for CH4-pyrolysis) because the CH4-drived hydrogen simulated a hydropyrolysis condition and facilitated dehydroaromatization reaction. CH4 also led to direct coupling, Diels-Alder, and co-aromatization reactions during the pyrolysis, contributing to enhancing the BTX yield. The addition of Ga to the HZSM-5 could further increase the BTX yield by means of facilitating hydrocracking/demethylation and methyl radical formation from CH4 assisting the generation of >C2 alkenes that could be further converted into BTX on acid sites of the HZSM-5.
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Quercus , Biocombustíveis , Biomassa , Catálise , Temperatura Alta , Metano , PiróliseRESUMO
The present study examined the effects of the pyrolysis environment on BTEX (benzene, toluene, ethylbenzene, and xylenes) production in the catalytic upgrading of yellow poplar pyrolysis vapors. Three different gas environments, N2, CH4, and pre-decomposed CH4 stream (10 wt%-Ni/5 wt%-La2O3-5 wt% CeO2-Al2O3), which is a mixture of H2 (55.62%) and CH4, were studied using two types of zeolite catalysts, HZSM-5, and 1 wt% Ga/HZSM-5. The BTEX yields were enhanced linearly in the order N2 < CH4 < CH4 ex-situ decomposition. The highest BTEX yield of 9.58 wt% was obtained under the CH4 ex-situ decomposition environment over 1 wt% Ga/HZSM-5. The methane and hydrocarbons derived from biomass were activated on highly dispersed (GaO)+ sites and transformed smoothly to BTEX by aromatization on the BrØnsted acid sites of Ga/HZSM-5. The hydrogen produced from methane decomposition also assisted in aromatics production through the hydrodeoxygenation of methoxyphenols, guaiacols and catechols.
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Liriodendron , Pirólise , Biomassa , Catálise , Temperatura Alta , Hidrogênio , MetanoRESUMO
The global economy is threatened by the depletion of fossil resources and fluctuations in fossil fuel prices, and thus it is necessary to exploit sustainable energy sources. Carbon-neutral fuels including bio-oil obtained from biomass pyrolysis can act as alternatives to fossil fuels. Co-pyrolysis of lignocellulosic biomass and plastic is efficient to upgrade the quality of bio-oil because plastic facilitates deoxygenation. However, catalysts are required to produce bio-oil that is suitable for potential use as transportation fuel. This review presents an overview of recent advances in catalytic co-pyrolysis of biomass and plastic from the perspective of chemistry, catalyst, and feedstock pretreatment. Additionally, this review introduces not only recent research results of acid catalysts for catalytic co-pyrolysis, but also recent approaches that utilize base catalysts. Future research directions are suggested for commercially feasible co-pyrolysis process.
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Petróleo , Plásticos , Biocombustíveis , Biomassa , Catálise , Temperatura Alta , Hidrocarbonetos , PiróliseRESUMO
Catalytic co-pyrolysis (CCP) of spent coffee ground (SCG) and cellulose over HZSM-5 and HY was characterized thermogravimetrically, and a catalytic pyrolysis of two samples was conducted using a tandem micro reactor that directly connected with gas chromatography-mass spectrometry. To access the more fundamental investigations on CCP, the effects of the zeolite pore structure, reaction temperature, in-situ/ex-situ reaction mode, catalyst to feedstock ratio, and the SCG and cellulose mixing ratio were experimentally evaluated. The temperature showing the highest thermal degradation rate of cellulose with SCG slightly delayed due to the interactions during the thermolysis of two samples. HZSM-5 in reference to HY produced more aromatic hydrocarbons from CCP. With respect to the reaction temperature, the formation of aromatic hydrocarbons increased with the pyrolytic temperature. Moreover, the in-situ/ex-situ reaction mode, catalyst/feedstock, and cellulose/SCG ratio were optimized to improve the aromatic hydrocarbon yield.
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Biocombustíveis , Celulose , Pirólise , Catálise , Café , Temperatura AltaRESUMO
Emulsification is a cost effective and simple method to use pyrolysis oil (or bio-oil) along with diesel as an emulsified fuel. Several combinations of emulsifiers, such as Span 80 and Atlox 4916, Span 80 and Zephrym PD3315, and Atlox 4916 and Zephrym PD3315, were tested to obtain stable emulsions. Two set of reactors (ultrasonicator and agitator-based mechanical reactor system) were used for the process. The ether-extracted pyrolysis oil (EEO), emulsifier, and diesel content of 10%-15%, 3%, and 82-87% were exposed to an ultrasonic power of 40% and with an agitation rate of 900 rpm. The emulsions obtained using Span 80 and Zephrym PD3315 showed stratification within 10 min. The emulsions for Span 80 and Atlox 4916 with a ratio of 3/15/82 for Emulsifer/EEO/Diesel, and for Atlox 4916 and Zephrym PD3315 emulsifiers with a ratio of 3/10/87 for Emulsifer/EEO/Diesel remained stable for more than 15 days. The functional groups analysis showed the stability of the emulsion for Span 80 and Atlox 4916, whereas a change in the absorbance intensity was observed when Atlox 4916 and Zephrym PD3315 were used, indicating stratification.
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Biocombustíveis , Éter , Pirólise , Emulsificantes , Éteres , Hexoses , PolietilenoglicóisRESUMO
The fast pyrolysis of waste lignin derived from biobutanol production process was performed to determine the optimal pyrolysis conditions and pyrolysis product properties. Four types of pyrolysis reactors, e.g.: micro-scale pyrolyzer-gas chromatography/mass spectrometry, lab and bench scale fixed bed (FB) reactors, and bench scale rotary kiln (RK) reactor, were employed to compare the pyrolysis reaction conditions and product properties obtained from different reactors. The yields of char, oil, and gas obtained from lab scale and bench scale reactor were almost similar compared to FB reactor. RK reactor produced desirable bio-oil with much reduced yield of poly aromatic hydrocarbons (cancer precursor) due to its higher cracking reaction efficiency. In addition, char agglomeration and foaming of lignin pyrolysis were greatly restricted by using RK reactor compared to the FB reactor.
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Lignina/química , Óleos de Plantas , Polifenóis , Butanóis/química , Hidrocarbonetos Policíclicos Aromáticos/análise , Pirólise , ResíduosRESUMO
Lignocellulosic biomass is an abundant renewable energy source that can be converted into various liquid fuels via thermochemical processes such as pyrolysis. Pyrolysis is a thermal decomposition method, in which solid biomass are thermally depolymerized to liquid fuel called bio-oil or pyrolysis oil. However, the low quality of pyrolysis oil caused by its high oxygen content necessitates further catalytic upgrading to increase the content of oxygen-free compounds, such as aromatic hydrocarbons. Among the three different types of lignocellulosic biomass components (hemicellulose, lignin, and cellulose), lignin is the most difficult fraction to be pyrolyzed because of its highly recalcitrant structure for depolymerization, forming a char as a main product. The catalytic conversion of lignin-derived pyrolyzates is also more difficult than that of furans and levoglucosan which are the main pyrolysis products of hemicellulose and cellulose. Hence, the main purpose of this study was to develop a bench-scale catalytic pyrolysis process using a tandem catalyst (both in-situ and ex-situ catalysis mode) for an efficient pyrolysis and subsequent upgrading of lignin components. While HZSM-5 was employed as an ex-situ catalyst for its excellent aromatization efficiency, the potential of the low-cost additives of bentonite, olivine, and spent FCC as in-situ catalysts in the Kraft lignin pyrolysis at 500⯰C was investigated. The effects of these in-situ catalysts on the product selectivity were studied; bentonite resulted in higher selectivity to aromatic hydrocarbons compared to olivine and spent FCC. The reusability of HZSM-5 (with and without regeneration) was examined in the pyrolysis of lignin mixed with the in-situ catalysts of bentonite, olivine, and spent FCC. In the case of using bentonite and spent FCC as in-situ catalysts, there were no obvious changes in the activity of HZSM-5 after regeneration, whereas using olivine as in-situ catalyst resulted in a remarkable decrease in the activity of HZSM-5 after regeneration.
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Bentonita , Compostos de Ferro , Lignina , Compostos de Magnésio , Óleos de Plantas , Polifenóis , Silicatos , Bentonita/química , Biocombustíveis , Biomassa , Catálise , Argila/química , Temperatura Alta , Compostos de Ferro/química , Lignina/química , Compostos de Magnésio/química , Óleos de Plantas/química , Polifenóis/química , Silicatos/químicaRESUMO
The concerns over the increasing energy demand and cost as well as environmental problems derived from fossil fuel use are the main driving forces of research into renewable energy. Lignocellulosic biomass comprised of cellulose, hemicellulose, and lignin is an abundant, carbon neutral, and alternative resource for replacing fossil fuels in the future. Solvent liquefaction of lignocellulosic biomass is a promising route to obtain biofuels, bio-based materials, and chemicals using a range of solvents as reaction media under moderate reaction conditions. Recently, several researchers have considered novel approaches for enhancing the process efficiency and economics. This review article reports the state-of-the-art knowledge of lignocellulose liquefaction in the recent three years with the main focus on the feedstock, liquefaction technology, target products, and degradation mechanism of each biomass component. This review is expected to provide an important reference for research into the solvent liquefaction of lignocellulose in the near future.