Electrochemical conversion of lignin for the production of high-value heterocyclic aromatic compounds has great potential.We demonstrate the targeted synthesis and cation modulation of NiCo_(2)O_(4)spinel nanoboxes,sy...Electrochemical conversion of lignin for the production of high-value heterocyclic aromatic compounds has great potential.We demonstrate the targeted synthesis and cation modulation of NiCo_(2)O_(4)spinel nanoboxes,synthesized via cation exchange and calcination oxidation.These catalysts exhibit excellent efficacy in the electrocatalytic conversion of lignin model compounds,specifically 2-phenoxy-1-phenylethanol,into nitrogen-containing aromatics,achieving high conversion rates and selectivities.These catalysts were synthesized via a cation exchange and calcination oxidation process,using Prussian blue nanocubes as precursors.The porous architecture and polymetallic composition of the NiCo_(2)O_(4)spinel demonstrated superior performance in electrocatalytic oxidative coupling,achieving a 99.2 wt%conversion rate of the 2-phenoxy-1-phenylethanol with selectivities of 37.5 wt%for quinoline derivatives and 31.5 wt%for phenol.Key innovations include the development of a sustainable one-pot synthesis method for quinoline derivatives,the elucidation of a multistage reaction pathway involving CAO bond cleavage,hydroxyaldol condensation,and CAN bond formation,and a deeper mechanistic understanding derived from DFT simulations.This work establishes a new strategy for lignin valorization,offering a sustainable route to produce high-value nitrogen-containing aromatics from renewable biomass under mild conditions,without the need for additional reagents.展开更多
Carbon fibers(CFs)with notable comprehensive properties,such as light weight,high specific strength,and stiffness,have garnered considerable interest in both academic and industrial fields due to their diverse and adv...Carbon fibers(CFs)with notable comprehensive properties,such as light weight,high specific strength,and stiffness,have garnered considerable interest in both academic and industrial fields due to their diverse and advanced applications.However,the commonly utilized precursors,such as polyacrylonitrile and pitch,exhibit a lack of environmental sustainability,and their costs are heavily reliant on fluctuating petroleum prices.To meet the substantial market demand for CFs,significant efforts have been made to develop cost-effective and sustainable CFs derived from biomass.Lignin,the most abundant polyphenolic compound in nature,is emerging as a promising precursor which is well-suited for the production of CFs due to its renewable nature,low cost,high carbon content,and aromatic structures.Nevertheless,the majority of lignin raw materials are currently derived from pulping and biorefining industrial by-products,which are diverse and heterogeneous in nature,restricting the industrialization of lignin-derived CFs.This review classifies fossil-derived and biomass-derived CFs,starting from the sources and chemical structures of raw lignin,and outlines the preparation methods linked to the performance of lignin-derived CFs.A comprehensive discussion is presented on the relationship between the structural characteristics of lignin,spinning preparation,and structure-morphology-property of ligninderived CFs.Additionally,the potential applications of these materials in various domains,including energy,catalysis,composites,and other advanced products,are also described with the objective of spotlighting the unique merits of lignin.Finally,the current challenges faced and future prospects for the advancement of lignin-derived CFs are proposed.展开更多
Directed degradation of abundant renewable lignin into small aromatic compounds is crucial for lignin valorization but challenging.The degradation of lignin in natural environments typically involves multienzyme syner...Directed degradation of abundant renewable lignin into small aromatic compounds is crucial for lignin valorization but challenging.The degradation of lignin in natural environments typically involves multienzyme synergy.However,the proteinaceous characteristics of lignin-degrading enzymes restrict their accessibility to certain regions of intricate lignin,resulting in the multienzyme systems being unable to fully demonstrate their effectiveness.Herein,a de novo biomimetic enzyme-nanozyme hybrid system was constructed by combiningλ-MnO_(2) nanozyme with laccase CotA from Bacillus subtilis,aimed at facilitating lignin degradation under mild conditions.The lignin degradation rate of the CotA+λ-MnO_(2) hybrid system was determined to be 25.15%,which was much higher than those of the lignin degradation systems with only laccase CotA(15.32%)orλ-MnO_(2) nanozyme(14.90%).Notably,the proportion of aromatic chemicals in the products derived from the hybrid system reached as much as 48%,which was 41.2%and 118.2%higher than those of the CotA-andλ-MnO_(2)-catalyzed systems,respectively.Analysis of products mapping and lignin structure changes suggested that the higher proportion of aromatic compounds in the CotA+λ-MnO_(2)hybrid system was more likely to benefit from the laccase-mediated methoxylation.Moreover,electron paramagnetic resonance analysis indicated that the intensity and kind of free radicals such as·OH and·O_(2)^(-)are closely linked to the degradation rate and reaction type.This work is the inaugural application of an enzyme-nanozyme hybrid system for lignin degradation,demonstrating the potential of the synergistic interaction between enzyme and nanozyme in the directed degradation of lignin.展开更多
Furfuryl ethyl ether(FEE)is considered as one of the most important candidates for biofuels due to its high-octane number.However,it is still challenging to produce FEE via the biomass-based route under mild condition...Furfuryl ethyl ether(FEE)is considered as one of the most important candidates for biofuels due to its high-octane number.However,it is still challenging to produce FEE via the biomass-based route under mild conditions.Here,we developed a photoinduced catalytic transfer hydrogenation(CTH)process for the efficient production of FEE through the reduction etherification of furfural(FF)using Na_(4)W_(10)O_(32)(NaDT),Pd/C,and ethanol as the hydrogen atom transfer(HAT)catalyst,hydrogenation catalyst,and the H donor,respectively.Notably,the introduction of brominated benzene(PhBr)as an additive significantly promoted the yield of FEE to 92.7%.A series of experiments and characterization results indicated that the attachment and detachment of Br atoms on Pd/C catalyst surface effectively regulate the balance between H^(+)sites and Pd sites in the NaDT+Pd/C catalytic system.The balance facilitates the preferential acetalization of FF catalyzed by H^(+)sites,followed by hydrogenation to efficiently produce FEE catalyzed by Pd sites.This photoinduced CTH process exhibits good stability and recyclability as well as universality for the transformation of various organic substrates under mild conditions.展开更多
Saccharification of lignocellulosic wastes is the bottleneck of different bio-based chemical industries.Using enzymes for saccharification of lignocellulosic materials has several advantages over using chemicals.In th...Saccharification of lignocellulosic wastes is the bottleneck of different bio-based chemical industries.Using enzymes for saccharification of lignocellulosic materials has several advantages over using chemicals.In the current work,the application of the Maximyze■ enzyme system,which is industrially used in papermaking,was investigated in the saccharification of paper sludge and fiber dust wastes from the tissue paper industry.For optimizing the saccharification process,the effects of the consistency%,enzyme loading,and incubation time were studied and optimized using the Response Surface Methodology.The effect of these factors on the weight loss of paper sludge and total sugars in the hydrolyzate was studied.High-Performance Liquid Chromatography(HPLC)was used to measure the sugars composition of the hydrolyzate.Under the optimized conditions,~90% and~66% of the fiber dust and paper sludge could be hydrolyzed into sugars,respectively.The sugar composition was 80.23% glucose,10.99% xylose,and 8.65% arabinose based on the total sugars in the case of fiber dust.In comparison,80.63% glucose,8.43% xylose,and 10.75% arabinose were detected in the case of paper sludge.The results showed the applicability of the Maximyze Rcommercial enzymes used in the paper industry for efficient saccharification of paper sludge and fiber dust.The presence of non-cellulosic materials in the paper sludge(residual ink,paper additives,and ash)didn’t affect the activity of the enzymes.The study also showed the potential use of fiber dust as a valuable and clean source of sugars that can be used to prepare different bio-based chemicals.展开更多
Photocatalytic transformation of biomass into biofuels and value-added chemicals is of great significance for carbon neutrality.Metal-free carbon nitride has extensive applications but with almost no absorption and ut...Photocatalytic transformation of biomass into biofuels and value-added chemicals is of great significance for carbon neutrality.Metal-free carbon nitride has extensive applications but with almost no absorption and utilization of near-infrared light,accounting for 50%of sunlight.Here,a molten salt-assisted in-plane“stitching”and interlayer“cutting”protocol is developed for constructing a highly crystalline carbon nitride catalyst containing structural oxygen(HC-CN).HC-CN is highly efficient for the photothermal cascade transformation of biomass-derived glucose into lactic acid(LA)with an unprecedented yield(94.3%)at 25°C under full-spectrum light irradiation within 50 min,which is also applicable to quantitatively photo-upgrading various saccharides.Theoretical calculations expound that the light-induced glucose-to-catalyst charge transfer can activate the Cβ-H bond to promote the rate-determining step of intramolecular hydrogen shift in glucose-to-fructose isomerization.Meanwhile,the introduced structural oxygen in HC-CN can not only facilitate the local electric field formation to achieve rapid charge transport/separation and regulate selective·O^(-)_(2)generation for oriented C3-C4 bond cleavage of fructose but also narrow the energy band gap to broaden the light absorption range of HC-CN,contributing to enhanced LA production without exogenous heating.Moreover,HC-CN is highly recyclable and exhibits negligible environmental burden and low energy consumption,as disclosed by the life cycle assessment.Tailored construction of full-spectrum light adsorption and versatile reaction sites provides a reference for implementing multi-step biomass and organic conversion processes under mild conditions.展开更多
On May 7,2025,Chinese President Xi Jinping published a signed article titled"Learning from History to Build Together a Brighter Future"in Russian newspaper Gazette ahead of his arrival in Moscow for a state ...On May 7,2025,Chinese President Xi Jinping published a signed article titled"Learning from History to Build Together a Brighter Future"in Russian newspaper Gazette ahead of his arrival in Moscow for a state visit to Russia and attendance at the celebration marking the 80th anniversary of the Victory in the Soviet Union's Great Patriotic War.展开更多
This paper presents findings of a study on solid wastes conversion into fuels through pyrolysis of plastic materials, presenting an alternative renewable approach for waste management. Investigations were conducted on...This paper presents findings of a study on solid wastes conversion into fuels through pyrolysis of plastic materials, presenting an alternative renewable approach for waste management. Investigations were conducted on conversion of polypropylene (PP), low-density polyethylene (LDPE) and high-density polyethylene (HDPE) under normal and catalyst mediated process conditions. Plastic wastes were collected from various dumpsites in Nairobi and segregated using plastic resin codes to various classes. Samples were cleaned, dried and shredded to 2 mm and fed into a pyrolysis reactor. The pyrolysis process was conducted at between 220˚C and 420˚C. Pyrolysis gases were condensed in a shell and coil condenser and the incondensable gases were stored in gasbags. Liquid fuels were analysed using Gas chromatograph with a mass spectroscopic detector and Fourier Transform Infrared Spectrometry. The results revealed that the most optimal process conditions were a temperature range of 220˚C - 420˚C at a heating rate of 10˚C per minute. Under these conditions, the oil yields were 53.72% for PP, 62.10% for LDPE, and 64.14% for HDPE. As the heating rate increased from 10˚C/min to 20˚C/min, gas yields increased, rising from 28.05% to 31.12% in PP, 14.96% to 30.62% in LDPE, and 18.51% to 29.49% in HDPE. The introduction of Fe2O3 and Al2O3 catalyst significantly enhanced gas production during pyrolysis, increasing yields from 18% to 61% and 47% respectively.展开更多
Sustainable aviation fuel(SAF)production from biomass and biowaste streams is an attractive option for decarbonizing the aviation sector,one of the most-difficult-to-electrify transportation sectors.Despite ongoing co...Sustainable aviation fuel(SAF)production from biomass and biowaste streams is an attractive option for decarbonizing the aviation sector,one of the most-difficult-to-electrify transportation sectors.Despite ongoing commercialization efforts using ASTM-certified pathways(e.g.,lipid conversion,Fischer-Tropsch synthesis),production capacities are still inadequate due to limited feedstock supply and high production costs.New conversion technologies that utilize lignocellulosic feedstocks are needed to meet these challenges and satisfy the rapidly growing market.Combining bio-and chemo-catalytic approaches can leverage advantages from both methods,i.e.,high product selectivity via biological conversion,and the capability to build C-C chains more efficiently via chemical catalysis.Herein,conversion routes,catalysis,and processes for such pathways are discussed,while key challenges and meaningful R&D opportunities are identified to guide future research activities in the space.Bio-and chemo-catalytic conversion primarily utilize the carbohydrate fraction of lignocellulose,leaving lignin as a waste product.This makes lignin conversion to SAF critical in order to utilize whole biomass,thereby lowering overall production costs while maximizing carbon efficiencies.Thus,lignin valorization strategies are also reviewed herein with vital research areas identified,such as facile lignin depolymerization approaches,highly integrated conversion systems,novel process configurations,and catalysts for the selective cleavage of aryl C-O bonds.The potential efficiency improvements available via integrated conversion steps,such as combined biological and chemo-catalytic routes,along with the use of different parallel pathways,are identified as key to producing all components of a cost-effective,100%SAF.展开更多
The increasing demand for sustainable energy solutions necessitates innovative approaches to biomass utilization.This study introduces a comprehensive biorefinery model that valorizes poplar biomass into high-value pr...The increasing demand for sustainable energy solutions necessitates innovative approaches to biomass utilization.This study introduces a comprehensive biorefinery model that valorizes poplar biomass into high-value products,including ethanol,furfural,phenol,and biochar.These products not only serve as promising sources for biofuel and renewable chemicals but also contribute to pollution mitigation.The approach employs a biphasic pretreatment system utilizing p-toluenesulfonic acid,pentanol,and AlCl_(3) under optimized conditions(120℃ for 45 min),achieving remarkable efficiencies of 95.8%xylan removal,90.2%delignification,and 90.7%glucan recovery.The underlying mechanism,elucidated through density functional theory,demonstrates how the disruption of lignin-carbohydrate complexes via electrostatic and hydrogen-bonding interactions enhances product yields.The cellulose-rich substrate yielded 71.3 g/L ethanol,while solubilized xylan converted to 86.7%furfural without additional acid.Furthermore,lignin pyrolysis produced bio-oil containing over 45.2%phenolic compounds,while biochar demonstrated significant adsorptive capacity for perfluorooctanoic acid.Scaling this biorefinery model to process 140 million tons of poplar biomass annually reduces CO_(2)emissions by 75.3 million tons and provides socioeconomic savings of $17.3 billion,supporting sustainable industrial transformation.展开更多
Oxidative catalysis enables lignin depolymerization to yield carbonyl-containing aromatic chemicals for sustainable lignocellulose valorization.The oxidative depolymerization of lignin requires high oxygen pressure an...Oxidative catalysis enables lignin depolymerization to yield carbonyl-containing aromatic chemicals for sustainable lignocellulose valorization.The oxidative depolymerization of lignin requires high oxygen pressure and harsh conditions to trade off lignin’s structural complexity and limited solubility.Herein,we developed an oxidation system for lignin depolymerization using a single phosphomolybdic acid(H_(3)PMo_(12)O_(40))catalyst in acetic acid solvent to address the aforementioned issues.The entire catalytic system was operated under only 0.1 MPa O_(2) pressure,providing over 20 wt% of aromatic compounds containing aldehydes and carboxylic acids.Theoretical calculations combined with experimental analyses reveal structural transformations and redox behavior driven by the synergistic interaction between H_(3)PMo_(12)O_(40) and acetic acid.Mechanistic studies detected superoxide radicals,confirming the joint role of catalyst and solvent in oxygen activation,radicals stabilization,and enhanced reaction efficiency.A low-cost,commercially available catalyst with minimal oxygen demand offers a promising route to industrial-scale biomass refining.展开更多
Photocatalytic technology harnesses solar energy to facilitate chemical transformations,presenting significant potential in energy generation and environmental remediation.However,the conventional O_(2)evolution proce...Photocatalytic technology harnesses solar energy to facilitate chemical transformations,presenting significant potential in energy generation and environmental remediation.However,the conventional O_(2)evolution process is hindered by high reaction barriers and inefficiencies,which limit its widespread application.Therefore,exploring novel photocatalytic coupling strategies to replace water oxidation has become a key route to enhance the efficiency of H_(2)production.In this review,organic pollutants removal and the valorization of organics as substitutes for water oxidation coupling strategies for photocatalytic H_(2)production are comprehensively summarized.These strategies not only circumvent the high reaction barriers associated with O_(2)evolution to enhance the H_(2)production but also aid in the removing of organic pollutants or synthesis of value-added chemicals.We also present future research directions and underscore the significance of advanced catalyst design,in-depth analysis of reaction mechanisms,and systematic optimization strategies in realizing an efficient and sustainable photocatalytic process.This guidance is anticipated to provide theoretical and practical new insights for the future development of photocatalytic coupling reactions,fostering further explorations in the realm of renewable energy and environmental governance.展开更多
In this research,the antibacterial properties of a composite material prepared from agave bagasse cellulose fibers doped with silver nanoparticles and chitosan were studied.The development of composite materials with ...In this research,the antibacterial properties of a composite material prepared from agave bagasse cellulose fibers doped with silver nanoparticles and chitosan were studied.The development of composite materials with antibacterial properties and environmentally friendly based on cellulose fibers from agave bagasse with silver nanoparticles prepared by green synthesis and chitosan from shrimp waste enhances the value of these agro-industrial wastes and offers the opportunity for them to have biomedical applications since these raw materials have been poorly reported for this application.The antibacterial properties of chitosan and silver nanoparticles are already known.However,the combination of silver nanoparticles with cellulose fibers and chitosan has been studied poorly.Green synthesis of silver nanoparticles was carried out,and spherical shape nanoparticles with a size between 20 and 50 nm were obtained by ultraviolet-visible(UV-Vis)spectroscopy and transmission electron microscopy(TEM)analysis.Additionally,in this research,the cellulose obtained from agave bagasse,the chitosan extracted from shrimp shells,and the composite material were characterized by infrared spectroscopy,mechanical analysis,and antibacterial tests.A decrease in the growth of Escherichia coli bacteria with 100%growth inhibition on cellulose,chitosan,and silver nanoparticles composite material and an increase in mechanical properties from 13.67 MPa of cellulose pure to 110 MPa of composite material was observed.These findings support the idea that the composite material has potential use in wound care dressings for antibacterial care.展开更多
Photocatalytic oxygen reduction for hydrogen peroxide(H_(2)O_(2))synthesis presents a green and costeffective production method.However,achieving highly selective H_(2)O_(2)synthesis remains challenging,necessitating ...Photocatalytic oxygen reduction for hydrogen peroxide(H_(2)O_(2))synthesis presents a green and costeffective production method.However,achieving highly selective H_(2)O_(2)synthesis remains challenging,necessitating precise control over free radical reaction pathways and minimizing undesirable oxidative by-products.Herein,we report for the visible light-driven simultaneous co-photocatalytic reduction of O2to H_(2)O_(2)and oxidation of biomass using the atomic rubidium-nitride modified carbon nitride(CNRb).The optimized CNRb catalyst demonstrates a record photoreduction rate of 8.01 mM h^(-1)for H_(2)O_(2)generation and photooxidation rate of 3.75 mM h^(-1)for furfuryl alcohol to furoic acid,achieving a remarkable solar-to-chemical conversion(SCC)efficiency of up to 2.27%.Experimental characterizations and DFT calculation disclosed that the introducing atomic Rb–N configurations allows for the high-selective generation of superoxide radicals while suppressing hydroxyl free radical formation.This is because the Rb–N serves as the new alternative site to perceive a stronger connection position for O2adsorption and reinforce the capability to extract protons,thereby triggering a high selective redox product formation.This study holds great potential in precisely regulating reactive radical processes at the atomic level,thereby paving the way for efficient synthesis of H_(2)O_(2)coupled with biomass valorization.展开更多
With global carbon emissions continuing to rise,carbon dioxide(CO_(2))capture and resource utilization have become central challenges in achieving the“dual carbon”goals(carbon peak and carbon neutrality).Traditional...With global carbon emissions continuing to rise,carbon dioxide(CO_(2))capture and resource utilization have become central challenges in achieving the“dual carbon”goals(carbon peak and carbon neutrality).Traditional carbon capture and storage(CCS)technology can only temporarily sequester CO_(2),whereas emerging green catalytic technologies(photo/electro/thermal catalysis)enable the conversion of CO_(2) into high-value chemicals(e.g.,fuels,pharmaceutical intermediates),advancing the closure of the artificial carbon cycle[1,2].展开更多
A novel gas-phase electrocatalytic cell containing a low-temperature proton exchange membrane(PEM)was developed to electrochemically convert CO_2into organic compounds.Two different Cu-based cathode catalysts(Cu and C...A novel gas-phase electrocatalytic cell containing a low-temperature proton exchange membrane(PEM)was developed to electrochemically convert CO_2into organic compounds.Two different Cu-based cathode catalysts(Cu and Cu–C)were prepared by physical vapor deposition method(sputtering)and subsequently employed for the gas-phase electroreduction of CO_2at different temperatures(70–90°C).The prepared electrodes Cu and Cu–C were characterized by X-ray diffraction(XRD),X-ray photoemission spectroscopy(XPS)and scanning electron microscopy(SEM).As revealed,Cu is partially oxidized on the surface of the samples and the Cu and Cu–C cathodic catalysts were comprised of a porous,continuous,and homogeneous film with nanocrystalline Cu with a grain size of 16 and 8 nm,respectively.The influence of the applied current and temperature on the electro-catalytic activity and selectivity of these materials was investigated.Among the two investigated electrodes,the pure Cu catalyst film showed the highest CO_2specific electrocatalytic reduction rates and higher selectivity to methanol formation compared to the Cu–C electrode,which was attributed to the higher particle size of the former and lower Cu O/Cu ratio.The obtained results show potential interest for the possible use of electrical renewable energy for the transformation of CO_2into valuable products using low metal loading Cu based electrodes(0.5 mg Cu cm^(-2))prepared by sputtering.展开更多
Developing efficient approaches for lignin upgrading is of interest for the industrial production of chemicals and fuels from renewable biomass.Electrocatalytic lignin upgrading powered by renewable electricity operat...Developing efficient approaches for lignin upgrading is of interest for the industrial production of chemicals and fuels from renewable biomass.Electrocatalytic lignin upgrading powered by renewable electricity operating under gentle conditions(at or near ambient pressures and temperatures)enables a decentralized production of chemicals and fuels.Herein,we will cover the structures of lignin and review the recent advances in the electrocatalytic lignin upgrade,the electrocatalytic depolymerization of lignin,and the electrocatalytic upgrading of lignin monomers to value-added chemicals and fuels.Finally,we provide insights into the main challenges and future perspectives of this field.展开更多
Production of biochemicals from waste streams has been attracting increasing worldwide interest to achieve climate protection goals.Chain elongation(CE)for production of mediumchain carboxylic acids(MCCAs,especially c...Production of biochemicals from waste streams has been attracting increasing worldwide interest to achieve climate protection goals.Chain elongation(CE)for production of mediumchain carboxylic acids(MCCAs,especially caproate,enanthate and caprylate)from diverse biowaste has emerged as a potential economic and environmental technology for a sustainable society.The present mini review summarizes the research utilizing various synthetic or real waste-derived substrates available for MCCA production.Additionally,the microbial characteristics of the CE process are surveyed and discussed.Considering that a large proportion of recalcitrantly biodegradable biowaste and residues cannot be further utilized by CE systems and remain to be treated and disposed,we propose here a loop concept of bioconversion of biowaste to MCCAs making full use of the biowaste with zero emission.This could make possible an alternative technology for synthesis of value-added products from a wide range of biowaste,or even non-biodegradable waste(such as,plastics and rubbers).Meanwhile,the remaining scientific questions,unsolved problems,application potential and possible developments for this technology are discussed.展开更多
In this work,a dual-size MOF-derived Co catalyst(0.2Co_(1-NPs)@NC)composed of single atoms(Co_(1))and highly dispersed nanoparticles(Co NPs)was prepared by in-situ Zn evaporation for the highperformance conversion of ...In this work,a dual-size MOF-derived Co catalyst(0.2Co_(1-NPs)@NC)composed of single atoms(Co_(1))and highly dispersed nanoparticles(Co NPs)was prepared by in-situ Zn evaporation for the highperformance conversion of lignin-derived o-methoxyphenols(lignin oil)to cyclohexanols(up to 97%yield)via cascade demethoxylation and dearomatization.Theoretical calculations elaborated that the dual-size Co catalyst exhibited a cooperative effect in the selective demethoxylation process,in which the Co NPs could initially dissociate hydrogen at lower energies while Co1remarkably facilitated the cleavage of the C_(Ar)-OCH_(3)bond.Moreover,the intramolecular hydrogen bonds formed in the omethoxy-containing phenols were found to result in a decrease in the bond energy of the C_(Ar)-OCH_(3)bond,which was more prone to be activated by the dual-size Co sites.Notably,the pre-hydrogenated intermediate(e.g.,2-methoxycyclohexanol from guaiacol)is difficult to undergo demethoxylation,indicating that the selective C_(Ar)-OCH_(3)bond cleavage is a prerequisite for the synthesis of cyclohexanols.The 0.2Co_(1-NPs)@NC catalyst was highly recyclable with a neglect decline in activity during five consecutive cycles.This cooperative catalytic strategy based on the metal size effect opens new avenues for biomass upgrading via enhanced C-O bond cleavage of high selectivity.展开更多
基金National Natural Science Foundation of China (U23A6005 and 22078069)Project funded by China Postdoctoral Science Foundation (GZB20230172 and 2023M740748)。
文摘Electrochemical conversion of lignin for the production of high-value heterocyclic aromatic compounds has great potential.We demonstrate the targeted synthesis and cation modulation of NiCo_(2)O_(4)spinel nanoboxes,synthesized via cation exchange and calcination oxidation.These catalysts exhibit excellent efficacy in the electrocatalytic conversion of lignin model compounds,specifically 2-phenoxy-1-phenylethanol,into nitrogen-containing aromatics,achieving high conversion rates and selectivities.These catalysts were synthesized via a cation exchange and calcination oxidation process,using Prussian blue nanocubes as precursors.The porous architecture and polymetallic composition of the NiCo_(2)O_(4)spinel demonstrated superior performance in electrocatalytic oxidative coupling,achieving a 99.2 wt%conversion rate of the 2-phenoxy-1-phenylethanol with selectivities of 37.5 wt%for quinoline derivatives and 31.5 wt%for phenol.Key innovations include the development of a sustainable one-pot synthesis method for quinoline derivatives,the elucidation of a multistage reaction pathway involving CAO bond cleavage,hydroxyaldol condensation,and CAN bond formation,and a deeper mechanistic understanding derived from DFT simulations.This work establishes a new strategy for lignin valorization,offering a sustainable route to produce high-value nitrogen-containing aromatics from renewable biomass under mild conditions,without the need for additional reagents.
基金National Natural Science Foundation of China,Grant/Award Numbers:32171717,32271814Natural Science Foundation of Tianjin Municipality,Grant/Award Numbers:24JCJQJC00030,22JCYBJC01560,23JCZDJC00630China Postdoctoral Science Foundation,Grant/Award Number:2023M740562。
文摘Carbon fibers(CFs)with notable comprehensive properties,such as light weight,high specific strength,and stiffness,have garnered considerable interest in both academic and industrial fields due to their diverse and advanced applications.However,the commonly utilized precursors,such as polyacrylonitrile and pitch,exhibit a lack of environmental sustainability,and their costs are heavily reliant on fluctuating petroleum prices.To meet the substantial market demand for CFs,significant efforts have been made to develop cost-effective and sustainable CFs derived from biomass.Lignin,the most abundant polyphenolic compound in nature,is emerging as a promising precursor which is well-suited for the production of CFs due to its renewable nature,low cost,high carbon content,and aromatic structures.Nevertheless,the majority of lignin raw materials are currently derived from pulping and biorefining industrial by-products,which are diverse and heterogeneous in nature,restricting the industrialization of lignin-derived CFs.This review classifies fossil-derived and biomass-derived CFs,starting from the sources and chemical structures of raw lignin,and outlines the preparation methods linked to the performance of lignin-derived CFs.A comprehensive discussion is presented on the relationship between the structural characteristics of lignin,spinning preparation,and structure-morphology-property of ligninderived CFs.Additionally,the potential applications of these materials in various domains,including energy,catalysis,composites,and other advanced products,are also described with the objective of spotlighting the unique merits of lignin.Finally,the current challenges faced and future prospects for the advancement of lignin-derived CFs are proposed.
文摘Directed degradation of abundant renewable lignin into small aromatic compounds is crucial for lignin valorization but challenging.The degradation of lignin in natural environments typically involves multienzyme synergy.However,the proteinaceous characteristics of lignin-degrading enzymes restrict their accessibility to certain regions of intricate lignin,resulting in the multienzyme systems being unable to fully demonstrate their effectiveness.Herein,a de novo biomimetic enzyme-nanozyme hybrid system was constructed by combiningλ-MnO_(2) nanozyme with laccase CotA from Bacillus subtilis,aimed at facilitating lignin degradation under mild conditions.The lignin degradation rate of the CotA+λ-MnO_(2) hybrid system was determined to be 25.15%,which was much higher than those of the lignin degradation systems with only laccase CotA(15.32%)orλ-MnO_(2) nanozyme(14.90%).Notably,the proportion of aromatic chemicals in the products derived from the hybrid system reached as much as 48%,which was 41.2%and 118.2%higher than those of the CotA-andλ-MnO_(2)-catalyzed systems,respectively.Analysis of products mapping and lignin structure changes suggested that the higher proportion of aromatic compounds in the CotA+λ-MnO_(2)hybrid system was more likely to benefit from the laccase-mediated methoxylation.Moreover,electron paramagnetic resonance analysis indicated that the intensity and kind of free radicals such as·OH and·O_(2)^(-)are closely linked to the degradation rate and reaction type.This work is the inaugural application of an enzyme-nanozyme hybrid system for lignin degradation,demonstrating the potential of the synergistic interaction between enzyme and nanozyme in the directed degradation of lignin.
文摘Furfuryl ethyl ether(FEE)is considered as one of the most important candidates for biofuels due to its high-octane number.However,it is still challenging to produce FEE via the biomass-based route under mild conditions.Here,we developed a photoinduced catalytic transfer hydrogenation(CTH)process for the efficient production of FEE through the reduction etherification of furfural(FF)using Na_(4)W_(10)O_(32)(NaDT),Pd/C,and ethanol as the hydrogen atom transfer(HAT)catalyst,hydrogenation catalyst,and the H donor,respectively.Notably,the introduction of brominated benzene(PhBr)as an additive significantly promoted the yield of FEE to 92.7%.A series of experiments and characterization results indicated that the attachment and detachment of Br atoms on Pd/C catalyst surface effectively regulate the balance between H^(+)sites and Pd sites in the NaDT+Pd/C catalytic system.The balance facilitates the preferential acetalization of FF catalyzed by H^(+)sites,followed by hydrogenation to efficiently produce FEE catalyzed by Pd sites.This photoinduced CTH process exhibits good stability and recyclability as well as universality for the transformation of various organic substrates under mild conditions.
基金funding of the current work by the Science,Technology,and Innovation Funding Authority(STDF),Egypt,project no.46104:“Recycling of sludge wastes from paper industry via green technologies”.
文摘Saccharification of lignocellulosic wastes is the bottleneck of different bio-based chemical industries.Using enzymes for saccharification of lignocellulosic materials has several advantages over using chemicals.In the current work,the application of the Maximyze■ enzyme system,which is industrially used in papermaking,was investigated in the saccharification of paper sludge and fiber dust wastes from the tissue paper industry.For optimizing the saccharification process,the effects of the consistency%,enzyme loading,and incubation time were studied and optimized using the Response Surface Methodology.The effect of these factors on the weight loss of paper sludge and total sugars in the hydrolyzate was studied.High-Performance Liquid Chromatography(HPLC)was used to measure the sugars composition of the hydrolyzate.Under the optimized conditions,~90% and~66% of the fiber dust and paper sludge could be hydrolyzed into sugars,respectively.The sugar composition was 80.23% glucose,10.99% xylose,and 8.65% arabinose based on the total sugars in the case of fiber dust.In comparison,80.63% glucose,8.43% xylose,and 10.75% arabinose were detected in the case of paper sludge.The results showed the applicability of the Maximyze Rcommercial enzymes used in the paper industry for efficient saccharification of paper sludge and fiber dust.The presence of non-cellulosic materials in the paper sludge(residual ink,paper additives,and ash)didn’t affect the activity of the enzymes.The study also showed the potential use of fiber dust as a valuable and clean source of sugars that can be used to prepare different bio-based chemicals.
基金the Natural Science Foundation of China(22368014,22478087)the Guizhou Provincial S&T Project(GCC[2023]011,ZK[2022]011).
文摘Photocatalytic transformation of biomass into biofuels and value-added chemicals is of great significance for carbon neutrality.Metal-free carbon nitride has extensive applications but with almost no absorption and utilization of near-infrared light,accounting for 50%of sunlight.Here,a molten salt-assisted in-plane“stitching”and interlayer“cutting”protocol is developed for constructing a highly crystalline carbon nitride catalyst containing structural oxygen(HC-CN).HC-CN is highly efficient for the photothermal cascade transformation of biomass-derived glucose into lactic acid(LA)with an unprecedented yield(94.3%)at 25°C under full-spectrum light irradiation within 50 min,which is also applicable to quantitatively photo-upgrading various saccharides.Theoretical calculations expound that the light-induced glucose-to-catalyst charge transfer can activate the Cβ-H bond to promote the rate-determining step of intramolecular hydrogen shift in glucose-to-fructose isomerization.Meanwhile,the introduced structural oxygen in HC-CN can not only facilitate the local electric field formation to achieve rapid charge transport/separation and regulate selective·O^(-)_(2)generation for oriented C3-C4 bond cleavage of fructose but also narrow the energy band gap to broaden the light absorption range of HC-CN,contributing to enhanced LA production without exogenous heating.Moreover,HC-CN is highly recyclable and exhibits negligible environmental burden and low energy consumption,as disclosed by the life cycle assessment.Tailored construction of full-spectrum light adsorption and versatile reaction sites provides a reference for implementing multi-step biomass and organic conversion processes under mild conditions.
文摘On May 7,2025,Chinese President Xi Jinping published a signed article titled"Learning from History to Build Together a Brighter Future"in Russian newspaper Gazette ahead of his arrival in Moscow for a state visit to Russia and attendance at the celebration marking the 80th anniversary of the Victory in the Soviet Union's Great Patriotic War.
文摘This paper presents findings of a study on solid wastes conversion into fuels through pyrolysis of plastic materials, presenting an alternative renewable approach for waste management. Investigations were conducted on conversion of polypropylene (PP), low-density polyethylene (LDPE) and high-density polyethylene (HDPE) under normal and catalyst mediated process conditions. Plastic wastes were collected from various dumpsites in Nairobi and segregated using plastic resin codes to various classes. Samples were cleaned, dried and shredded to 2 mm and fed into a pyrolysis reactor. The pyrolysis process was conducted at between 220˚C and 420˚C. Pyrolysis gases were condensed in a shell and coil condenser and the incondensable gases were stored in gasbags. Liquid fuels were analysed using Gas chromatograph with a mass spectroscopic detector and Fourier Transform Infrared Spectrometry. The results revealed that the most optimal process conditions were a temperature range of 220˚C - 420˚C at a heating rate of 10˚C per minute. Under these conditions, the oil yields were 53.72% for PP, 62.10% for LDPE, and 64.14% for HDPE. As the heating rate increased from 10˚C/min to 20˚C/min, gas yields increased, rising from 28.05% to 31.12% in PP, 14.96% to 30.62% in LDPE, and 18.51% to 29.49% in HDPE. The introduction of Fe2O3 and Al2O3 catalyst significantly enhanced gas production during pyrolysis, increasing yields from 18% to 61% and 47% respectively.
基金supported by the Center for Bioenergy Innovation(CBI)supported by the Office of Biological and Environmental Research in the DOE Office of Science and led by Oak Ridge National Laboratory.Oak Ridge National Laboratory is managed by UT-Battelle,LLC for the US DOE under Contract Number DE-AC05-00OR22725+2 种基金authored in part by the Na-tional Renewable Energy Laboratory,operated by Alliance for Sustainable Energy,LLC,for the U.S.Department of Energy(DOE)under Contract No.DE-LC-000L054provided by the U.S.Department of Energy(DOE),Office of Energy Efficiency and Renewable Energy(EERE),and Bioenergy Technologies Office(BETO)at the Pacific Northwest National Laboratory(PNNL)under Contract No.DE-AC05-76RL01830supported by Laboratory Directed Research and Development(LDRD)funding from Argonne National Laboratory,provided by the Director,Office of Science,of the U.S.Department of Energy under Contract No.DE-AC02-06CH11357。
文摘Sustainable aviation fuel(SAF)production from biomass and biowaste streams is an attractive option for decarbonizing the aviation sector,one of the most-difficult-to-electrify transportation sectors.Despite ongoing commercialization efforts using ASTM-certified pathways(e.g.,lipid conversion,Fischer-Tropsch synthesis),production capacities are still inadequate due to limited feedstock supply and high production costs.New conversion technologies that utilize lignocellulosic feedstocks are needed to meet these challenges and satisfy the rapidly growing market.Combining bio-and chemo-catalytic approaches can leverage advantages from both methods,i.e.,high product selectivity via biological conversion,and the capability to build C-C chains more efficiently via chemical catalysis.Herein,conversion routes,catalysis,and processes for such pathways are discussed,while key challenges and meaningful R&D opportunities are identified to guide future research activities in the space.Bio-and chemo-catalytic conversion primarily utilize the carbohydrate fraction of lignocellulose,leaving lignin as a waste product.This makes lignin conversion to SAF critical in order to utilize whole biomass,thereby lowering overall production costs while maximizing carbon efficiencies.Thus,lignin valorization strategies are also reviewed herein with vital research areas identified,such as facile lignin depolymerization approaches,highly integrated conversion systems,novel process configurations,and catalysts for the selective cleavage of aryl C-O bonds.The potential efficiency improvements available via integrated conversion steps,such as combined biological and chemo-catalytic routes,along with the use of different parallel pathways,are identified as key to producing all components of a cost-effective,100%SAF.
基金funded by the National Natural Science Foundation of China(22278189,22478154)the Fundamental Research Funds for the Central Universities(Jiangnan University,JUSRP202501024)the Priority Academic Program Development of Jiangsu Higher Education Institutions,the 111 Project(No.111-2-06)。
文摘The increasing demand for sustainable energy solutions necessitates innovative approaches to biomass utilization.This study introduces a comprehensive biorefinery model that valorizes poplar biomass into high-value products,including ethanol,furfural,phenol,and biochar.These products not only serve as promising sources for biofuel and renewable chemicals but also contribute to pollution mitigation.The approach employs a biphasic pretreatment system utilizing p-toluenesulfonic acid,pentanol,and AlCl_(3) under optimized conditions(120℃ for 45 min),achieving remarkable efficiencies of 95.8%xylan removal,90.2%delignification,and 90.7%glucan recovery.The underlying mechanism,elucidated through density functional theory,demonstrates how the disruption of lignin-carbohydrate complexes via electrostatic and hydrogen-bonding interactions enhances product yields.The cellulose-rich substrate yielded 71.3 g/L ethanol,while solubilized xylan converted to 86.7%furfural without additional acid.Furthermore,lignin pyrolysis produced bio-oil containing over 45.2%phenolic compounds,while biochar demonstrated significant adsorptive capacity for perfluorooctanoic acid.Scaling this biorefinery model to process 140 million tons of poplar biomass annually reduces CO_(2)emissions by 75.3 million tons and provides socioeconomic savings of $17.3 billion,supporting sustainable industrial transformation.
文摘Oxidative catalysis enables lignin depolymerization to yield carbonyl-containing aromatic chemicals for sustainable lignocellulose valorization.The oxidative depolymerization of lignin requires high oxygen pressure and harsh conditions to trade off lignin’s structural complexity and limited solubility.Herein,we developed an oxidation system for lignin depolymerization using a single phosphomolybdic acid(H_(3)PMo_(12)O_(40))catalyst in acetic acid solvent to address the aforementioned issues.The entire catalytic system was operated under only 0.1 MPa O_(2) pressure,providing over 20 wt% of aromatic compounds containing aldehydes and carboxylic acids.Theoretical calculations combined with experimental analyses reveal structural transformations and redox behavior driven by the synergistic interaction between H_(3)PMo_(12)O_(40) and acetic acid.Mechanistic studies detected superoxide radicals,confirming the joint role of catalyst and solvent in oxygen activation,radicals stabilization,and enhanced reaction efficiency.A low-cost,commercially available catalyst with minimal oxygen demand offers a promising route to industrial-scale biomass refining.
基金financially supported by the National Natural Science Foundation of China(No.22202065)。
文摘Photocatalytic technology harnesses solar energy to facilitate chemical transformations,presenting significant potential in energy generation and environmental remediation.However,the conventional O_(2)evolution process is hindered by high reaction barriers and inefficiencies,which limit its widespread application.Therefore,exploring novel photocatalytic coupling strategies to replace water oxidation has become a key route to enhance the efficiency of H_(2)production.In this review,organic pollutants removal and the valorization of organics as substitutes for water oxidation coupling strategies for photocatalytic H_(2)production are comprehensively summarized.These strategies not only circumvent the high reaction barriers associated with O_(2)evolution to enhance the H_(2)production but also aid in the removing of organic pollutants or synthesis of value-added chemicals.We also present future research directions and underscore the significance of advanced catalyst design,in-depth analysis of reaction mechanisms,and systematic optimization strategies in realizing an efficient and sustainable photocatalytic process.This guidance is anticipated to provide theoretical and practical new insights for the future development of photocatalytic coupling reactions,fostering further explorations in the realm of renewable energy and environmental governance.
文摘In this research,the antibacterial properties of a composite material prepared from agave bagasse cellulose fibers doped with silver nanoparticles and chitosan were studied.The development of composite materials with antibacterial properties and environmentally friendly based on cellulose fibers from agave bagasse with silver nanoparticles prepared by green synthesis and chitosan from shrimp waste enhances the value of these agro-industrial wastes and offers the opportunity for them to have biomedical applications since these raw materials have been poorly reported for this application.The antibacterial properties of chitosan and silver nanoparticles are already known.However,the combination of silver nanoparticles with cellulose fibers and chitosan has been studied poorly.Green synthesis of silver nanoparticles was carried out,and spherical shape nanoparticles with a size between 20 and 50 nm were obtained by ultraviolet-visible(UV-Vis)spectroscopy and transmission electron microscopy(TEM)analysis.Additionally,in this research,the cellulose obtained from agave bagasse,the chitosan extracted from shrimp shells,and the composite material were characterized by infrared spectroscopy,mechanical analysis,and antibacterial tests.A decrease in the growth of Escherichia coli bacteria with 100%growth inhibition on cellulose,chitosan,and silver nanoparticles composite material and an increase in mechanical properties from 13.67 MPa of cellulose pure to 110 MPa of composite material was observed.These findings support the idea that the composite material has potential use in wound care dressings for antibacterial care.
基金National Natural Science Foundation of China(22309032,22109120,and 62104170)Guangdong Basic and Applied Basic Research Foundation(2022A1515011737)+2 种基金Science and Technology Program of Guangzhou(2023A04J1395)GDAS’Project of Science and Technology Development(2021GDASYL-20210102010)Zhejiang Provincial Natural Science Foundation of China(LY23F040001)。
文摘Photocatalytic oxygen reduction for hydrogen peroxide(H_(2)O_(2))synthesis presents a green and costeffective production method.However,achieving highly selective H_(2)O_(2)synthesis remains challenging,necessitating precise control over free radical reaction pathways and minimizing undesirable oxidative by-products.Herein,we report for the visible light-driven simultaneous co-photocatalytic reduction of O2to H_(2)O_(2)and oxidation of biomass using the atomic rubidium-nitride modified carbon nitride(CNRb).The optimized CNRb catalyst demonstrates a record photoreduction rate of 8.01 mM h^(-1)for H_(2)O_(2)generation and photooxidation rate of 3.75 mM h^(-1)for furfuryl alcohol to furoic acid,achieving a remarkable solar-to-chemical conversion(SCC)efficiency of up to 2.27%.Experimental characterizations and DFT calculation disclosed that the introducing atomic Rb–N configurations allows for the high-selective generation of superoxide radicals while suppressing hydroxyl free radical formation.This is because the Rb–N serves as the new alternative site to perceive a stronger connection position for O2adsorption and reinforce the capability to extract protons,thereby triggering a high selective redox product formation.This study holds great potential in precisely regulating reactive radical processes at the atomic level,thereby paving the way for efficient synthesis of H_(2)O_(2)coupled with biomass valorization.
基金supported by the National Natural Science Foundation of China(22472069,22102064,and 22302080)China Postdoctoral Science Foundation(2024M760028).
文摘With global carbon emissions continuing to rise,carbon dioxide(CO_(2))capture and resource utilization have become central challenges in achieving the“dual carbon”goals(carbon peak and carbon neutrality).Traditional carbon capture and storage(CCS)technology can only temporarily sequester CO_(2),whereas emerging green catalytic technologies(photo/electro/thermal catalysis)enable the conversion of CO_(2) into high-value chemicals(e.g.,fuels,pharmaceutical intermediates),advancing the closure of the artificial carbon cycle[1,2].
基金Financial support from the "Spanish Ministry of Economy, Industry, and Competitiveness" (Project CTQ2016-75491-R)from Abengoa Researchthe Spanish Ministry of Economy, Industry, and Competitiveness for financial support through the Ramón y Cajal Program, Grant: RYC-2015-19230
文摘A novel gas-phase electrocatalytic cell containing a low-temperature proton exchange membrane(PEM)was developed to electrochemically convert CO_2into organic compounds.Two different Cu-based cathode catalysts(Cu and Cu–C)were prepared by physical vapor deposition method(sputtering)and subsequently employed for the gas-phase electroreduction of CO_2at different temperatures(70–90°C).The prepared electrodes Cu and Cu–C were characterized by X-ray diffraction(XRD),X-ray photoemission spectroscopy(XPS)and scanning electron microscopy(SEM).As revealed,Cu is partially oxidized on the surface of the samples and the Cu and Cu–C cathodic catalysts were comprised of a porous,continuous,and homogeneous film with nanocrystalline Cu with a grain size of 16 and 8 nm,respectively.The influence of the applied current and temperature on the electro-catalytic activity and selectivity of these materials was investigated.Among the two investigated electrodes,the pure Cu catalyst film showed the highest CO_2specific electrocatalytic reduction rates and higher selectivity to methanol formation compared to the Cu–C electrode,which was attributed to the higher particle size of the former and lower Cu O/Cu ratio.The obtained results show potential interest for the possible use of electrical renewable energy for the transformation of CO_2into valuable products using low metal loading Cu based electrodes(0.5 mg Cu cm^(-2))prepared by sputtering.
文摘Developing efficient approaches for lignin upgrading is of interest for the industrial production of chemicals and fuels from renewable biomass.Electrocatalytic lignin upgrading powered by renewable electricity operating under gentle conditions(at or near ambient pressures and temperatures)enables a decentralized production of chemicals and fuels.Herein,we will cover the structures of lignin and review the recent advances in the electrocatalytic lignin upgrade,the electrocatalytic depolymerization of lignin,and the electrocatalytic upgrading of lignin monomers to value-added chemicals and fuels.Finally,we provide insights into the main challenges and future perspectives of this field.
基金supported by the National Natural Science Foundation of China (Nos. 51622809, 51878471)
文摘Production of biochemicals from waste streams has been attracting increasing worldwide interest to achieve climate protection goals.Chain elongation(CE)for production of mediumchain carboxylic acids(MCCAs,especially caproate,enanthate and caprylate)from diverse biowaste has emerged as a potential economic and environmental technology for a sustainable society.The present mini review summarizes the research utilizing various synthetic or real waste-derived substrates available for MCCA production.Additionally,the microbial characteristics of the CE process are surveyed and discussed.Considering that a large proportion of recalcitrantly biodegradable biowaste and residues cannot be further utilized by CE systems and remain to be treated and disposed,we propose here a loop concept of bioconversion of biowaste to MCCAs making full use of the biowaste with zero emission.This could make possible an alternative technology for synthesis of value-added products from a wide range of biowaste,or even non-biodegradable waste(such as,plastics and rubbers).Meanwhile,the remaining scientific questions,unsolved problems,application potential and possible developments for this technology are discussed.
基金the Guizhou Provincial S&T Project(ZK[2022]011)the National Natural Science Foundation of China(21908033,21922513)+1 种基金the Natural Science Foundation of Guangxi Zhuang Autonomous Region(2020GXNSFAA297072)the Fok Ying-Tong Education Foundation(161030)。
文摘In this work,a dual-size MOF-derived Co catalyst(0.2Co_(1-NPs)@NC)composed of single atoms(Co_(1))and highly dispersed nanoparticles(Co NPs)was prepared by in-situ Zn evaporation for the highperformance conversion of lignin-derived o-methoxyphenols(lignin oil)to cyclohexanols(up to 97%yield)via cascade demethoxylation and dearomatization.Theoretical calculations elaborated that the dual-size Co catalyst exhibited a cooperative effect in the selective demethoxylation process,in which the Co NPs could initially dissociate hydrogen at lower energies while Co1remarkably facilitated the cleavage of the C_(Ar)-OCH_(3)bond.Moreover,the intramolecular hydrogen bonds formed in the omethoxy-containing phenols were found to result in a decrease in the bond energy of the C_(Ar)-OCH_(3)bond,which was more prone to be activated by the dual-size Co sites.Notably,the pre-hydrogenated intermediate(e.g.,2-methoxycyclohexanol from guaiacol)is difficult to undergo demethoxylation,indicating that the selective C_(Ar)-OCH_(3)bond cleavage is a prerequisite for the synthesis of cyclohexanols.The 0.2Co_(1-NPs)@NC catalyst was highly recyclable with a neglect decline in activity during five consecutive cycles.This cooperative catalytic strategy based on the metal size effect opens new avenues for biomass upgrading via enhanced C-O bond cleavage of high selectivity.
