Catalytic hydrodeoxygenation(HDO)is one of the most promising strategies to transform oxygen-rich biomass derivatives into high value-added chemicals and fuels,but highly challenging due to the lack of highly efficien...Catalytic hydrodeoxygenation(HDO)is one of the most promising strategies to transform oxygen-rich biomass derivatives into high value-added chemicals and fuels,but highly challenging due to the lack of highly efficient nonprecious metal catalysts.Herein,we report for the first time of a facile synthetic approach to controllably fabricate well-defined Ni-Co alloy NPs confined on the tip of N-CNTs as HDO catalyst.The resultant Ni-Co alloy catalyst possesses outstanding HDO performance towards biomass-derived vanillin into 2-methoxy-4-methylphenol in water with 100%conversion efficiency and selectivity under mild reaction conditions,surpassing the reported high performance nonprecious HDO catalysts.Impressively,our experimental results also unveil that the Ni-Co alloy catalyst can be generically applied to catalyze HDO of vanillin derivatives and other aromatic aldehydes in water with 100%conversion efficiency and over 90%selectivity.Importantly,our DFT calculations and experimental results confirm that the achieved outstanding HDO catalytic performance is due to the greatly promoted selective adsorption and activation of C=O,and desorption of the activated hydrogen species by the synergism of the alloyed Ni-Co NPs.The findings of this work affords a new strategy to design and develop efficient transition metal-based catalysts for HDO reactions in water.展开更多
Enhancing awareness of personal cleanliness and antibacterial resistance has intensified the antibacterial substance request on consumable products. Antibacterial agents that have been commercialized nowadays are prod...Enhancing awareness of personal cleanliness and antibacterial resistance has intensified the antibacterial substance request on consumable products. Antibacterial agents that have been commercialized nowadays are produced from inorganic and non-renewable substances. This provides several drawbacks, particularly against health and environmental issues. Therefore, many scientists work on substituting fossil-fuel-based antibacterial agents with natural ones such as from biomass. Biomass derivatives, natural abundances of biopolymers in the world, amount to major compounds including polysaccharides (cellulose, hemicellulose, and chitosan) and polyphenol (tannin and lignin) substances which are capable to combat the growth of Gram-positive bacteria and Gram-negative bacteria. To date, no report focuses on a deep understanding of antibacterial properties derived from biomass and the internal and external factors effects. This work provides that gap because comprehensive knowledge is necessary before applying biomass to the products. The potency of biomass derivatives as antibacterial additives is also summarized. Basic knowledge of antibacterial characteristics to the application in products is highlighted in this review. Besides, the discussion about challenges and future perspectives is also delivered.展开更多
Photocatalytic reductive amination of biomass-derived aldehydes is a desirable way to selectively upgrade biomass into value-added nitrogen-containing chemicals under mild conditions.However,it is challenging to produ...Photocatalytic reductive amination of biomass-derived aldehydes is a desirable way to selectively upgrade biomass into value-added nitrogen-containing chemicals under mild conditions.However,it is challenging to produce imines in high selectivity because of the undesirable side reactions caused by the activity of functional groups.Here,we demonstrate the highly reactive and selective production of imines from biomass derived aldehydes via the photocatalytic reductive amination,using a defective TiO_(2)supported nickel catalyst.The employment of methanol as the hydrogen donor and ammonia solution as the nitrogen source avoids the use of high-pressure H_(2)and expensive amines,rendering the current catalytic process safe,economical,and environmentally friendly.In depth investigations attribute the improved separation and transfer of photogenerated charge carriers to the presence of oxygen vacancies and decorated Ni nanoparticles,thereby accelerating the production of imines from benzaldehyde amination(conversion,95.8%;seleetivity,95.2%).Furthermore,the developed system could be easily translated to the photocatalytic conversions of various biomass derived aldehydes,which provided an example of a cost-effective and sustainable approach for the valorization of biomass derived feedstocks.展开更多
Electrocatalytic n-valeraldehyde oxidation reaction was an inexpensive and eco-friendly method to control n-valeraldehyde contamination and produce high value-added octane.However,low-cost and readily available electr...Electrocatalytic n-valeraldehyde oxidation reaction was an inexpensive and eco-friendly method to control n-valeraldehyde contamination and produce high value-added octane.However,low-cost and readily available electrocatalysts with high current efficiency were urgently needed.Herein,two-dimensional porous carbon derived from pollen with enlarged interlayer distance was built by alkali activation method,applying in electrocatalytic n-valeraldehyde oxidation reaction.The enlarged interlayer distance was verified by X-ray diffraction(XRD)and high-angle annular dark-field scanning transmission electron microscope(HAADF-STEM).Electrocatalytic experiments consequences showed activated biomass derived carbon possessed a higher electrocatalytic activity and octane selectivity than unactivated catalyst.Systematic tests and in situ infrared experiments demonstrated that enlarged interlayer distance was positively correlated with specific surface area of catalysts,large specific surface area provided abundant absorption sites,facilitated the adsorption for n-valeraldehyde,and further promoted the transformation of n-valeraldehyde to octane.This work also provides a new avenue for creating high-performance electrocatalysts in terms of lattice engineering.展开更多
Electromagnetic(EM)wave absorbers with wideband absorption capability are proposed as a strategy to mitigate environmental pollution by EM waves.However,designing an EM absorber with its performance capacity independe...Electromagnetic(EM)wave absorbers with wideband absorption capability are proposed as a strategy to mitigate environmental pollution by EM waves.However,designing an EM absorber with its performance capacity independent of the EM wave incident angle remains elusive to date.Resolving this challenge requires development of EM absorbers whose EM absorption performance is insensitive to the EM wave incident angle.Herein,we synthesized EM absorbers with a variety of structures with different symme-tries(including micro-/nanospheres,nanoflakes and nanotubes)to study the effect of the EM absorbers’structure and the EM wave incident angle on the EM absorption performance.Our analysis reveals that non-magnetic EM absorbers with spatially symmetric nanostructures exhibit excellent EM wave incident angle-insensitivity.Finally,we demonstrate that a class of non-magnetic EM absorbers made from bam-boo derived-carbon nanospheres exhibit EM incident angle-insensitivity and wideband EM absorption performance with an effective absorption band up to 3.5 GHz when the thickness is 1.4 mm,a signif-icant improvement from prior studies which used thicknesses as high as 3-4 mm for comparable EM absorption performance.展开更多
This study focuses on a CFD modelling of biomass-derived syngas co-firing with coal in an older mid-sized PC-fired boiler of type OP-230 with low-emission burners on the front wall. The simulations were performed to d...This study focuses on a CFD modelling of biomass-derived syngas co-firing with coal in an older mid-sized PC-fired boiler of type OP-230 with low-emission burners on the front wall. The simulations were performed to determine whether the boiler can be retrofitted for the fulfilment of the prospective environmental protection regulations relating to levels of NO_X emissions. The improvement of the air staging via the dual-fuel technique was based on the indirect co-firing technology. The impact of two arrangements of dedicated syngas nozzles(below and above the existing coal burners), two syngas compositions and two heat replacements(5% and 15%) on the course of thermal processes in a furnace was tested. The reductions in NO_X emissions were predicted relative to the baseline when only coal is combusted. The highest reduction of about 38% was achieved with the syngas nozzles below the existing coal burners and 15% heat replacement. This arrangement of nozzles offers the residence time sufficient to co-fire coal with waste derived syngas. A lower reduction in NO_X emissions was obtained with the nozzles above the burners as the enlargement of local fuel rich zone near syngas injection becomes significant for 15% heat replacement. Results provide for the decreasing impact of methane content along with the increase of syngas heat input. The avoided CO_2 emissions through the syngas indirect co-firing with coal in the boiler are linear function of heat replacements.展开更多
文摘Catalytic hydrodeoxygenation(HDO)is one of the most promising strategies to transform oxygen-rich biomass derivatives into high value-added chemicals and fuels,but highly challenging due to the lack of highly efficient nonprecious metal catalysts.Herein,we report for the first time of a facile synthetic approach to controllably fabricate well-defined Ni-Co alloy NPs confined on the tip of N-CNTs as HDO catalyst.The resultant Ni-Co alloy catalyst possesses outstanding HDO performance towards biomass-derived vanillin into 2-methoxy-4-methylphenol in water with 100%conversion efficiency and selectivity under mild reaction conditions,surpassing the reported high performance nonprecious HDO catalysts.Impressively,our experimental results also unveil that the Ni-Co alloy catalyst can be generically applied to catalyze HDO of vanillin derivatives and other aromatic aldehydes in water with 100%conversion efficiency and over 90%selectivity.Importantly,our DFT calculations and experimental results confirm that the achieved outstanding HDO catalytic performance is due to the greatly promoted selective adsorption and activation of C=O,and desorption of the activated hydrogen species by the synergism of the alloyed Ni-Co NPs.The findings of this work affords a new strategy to design and develop efficient transition metal-based catalysts for HDO reactions in water.
基金Besides,thanks for financing assistance(No.SKPB6412/LPDP/LPDP.3/2023)from the Indonesia Endowment Fund for Education(LPDP).
文摘Enhancing awareness of personal cleanliness and antibacterial resistance has intensified the antibacterial substance request on consumable products. Antibacterial agents that have been commercialized nowadays are produced from inorganic and non-renewable substances. This provides several drawbacks, particularly against health and environmental issues. Therefore, many scientists work on substituting fossil-fuel-based antibacterial agents with natural ones such as from biomass. Biomass derivatives, natural abundances of biopolymers in the world, amount to major compounds including polysaccharides (cellulose, hemicellulose, and chitosan) and polyphenol (tannin and lignin) substances which are capable to combat the growth of Gram-positive bacteria and Gram-negative bacteria. To date, no report focuses on a deep understanding of antibacterial properties derived from biomass and the internal and external factors effects. This work provides that gap because comprehensive knowledge is necessary before applying biomass to the products. The potency of biomass derivatives as antibacterial additives is also summarized. Basic knowledge of antibacterial characteristics to the application in products is highlighted in this review. Besides, the discussion about challenges and future perspectives is also delivered.
基金financially supported by the National Natural Science Foundation of China(Nos.22202105,22002043 and 22205113)the Natural Science Foundation of Jiangsu Province(Nos.BK20210608 and BK20210626)+1 种基金the Natural Science Foundation of Jiangsu Higher Education Institutions of China(Nos.21KJA150003 and 21KJB150027)the China Postdoctoral Science Foundation(No.2022M711645)。
文摘Photocatalytic reductive amination of biomass-derived aldehydes is a desirable way to selectively upgrade biomass into value-added nitrogen-containing chemicals under mild conditions.However,it is challenging to produce imines in high selectivity because of the undesirable side reactions caused by the activity of functional groups.Here,we demonstrate the highly reactive and selective production of imines from biomass derived aldehydes via the photocatalytic reductive amination,using a defective TiO_(2)supported nickel catalyst.The employment of methanol as the hydrogen donor and ammonia solution as the nitrogen source avoids the use of high-pressure H_(2)and expensive amines,rendering the current catalytic process safe,economical,and environmentally friendly.In depth investigations attribute the improved separation and transfer of photogenerated charge carriers to the presence of oxygen vacancies and decorated Ni nanoparticles,thereby accelerating the production of imines from benzaldehyde amination(conversion,95.8%;seleetivity,95.2%).Furthermore,the developed system could be easily translated to the photocatalytic conversions of various biomass derived aldehydes,which provided an example of a cost-effective and sustainable approach for the valorization of biomass derived feedstocks.
基金supported by Liaoning Technical Innovation Center of Industrial Ecology and Environmental Engineering,Shandong Provincial Natural Science Foundation(No.ZR2021QB048)Qingdao Postdoctoral Application Research Funded Project(Nos.QDBSH20220201046,QDBSH20230202062)+3 种基金Scientific Research Foundation for Youth Scholars from Qingdao University,National Natural Science Foundation of China(Nos.51473082,51878361)State Key Project of International Cooperation Research(No.2023YFE0201100)the Program for Introducing Talents of Discipline to Universities(“111”plan)the double hundred foreign expert project of Shandong Province,and the high-level discipline program of Materials Science of Shandong Province,China.
文摘Electrocatalytic n-valeraldehyde oxidation reaction was an inexpensive and eco-friendly method to control n-valeraldehyde contamination and produce high value-added octane.However,low-cost and readily available electrocatalysts with high current efficiency were urgently needed.Herein,two-dimensional porous carbon derived from pollen with enlarged interlayer distance was built by alkali activation method,applying in electrocatalytic n-valeraldehyde oxidation reaction.The enlarged interlayer distance was verified by X-ray diffraction(XRD)and high-angle annular dark-field scanning transmission electron microscope(HAADF-STEM).Electrocatalytic experiments consequences showed activated biomass derived carbon possessed a higher electrocatalytic activity and octane selectivity than unactivated catalyst.Systematic tests and in situ infrared experiments demonstrated that enlarged interlayer distance was positively correlated with specific surface area of catalysts,large specific surface area provided abundant absorption sites,facilitated the adsorption for n-valeraldehyde,and further promoted the transformation of n-valeraldehyde to octane.This work also provides a new avenue for creating high-performance electrocatalysts in terms of lattice engineering.
基金financial support from the startup fund of the Ohio State University (OSU)OSU Sustainability Institute Seed Grant+5 种基金OSU Institute for Materials Research Kickstart Facility Grantthe National Natural Science Foundation of China (No. 31971740)support from the National Natural Science Foundation of China (No. 31901007)Science and technology project of Jiangsu Province (BE2018391)State Key Laboratory Special Fund(No. 2060204)fund from Henan University of Science and Technology (2020-RSC02)
文摘Electromagnetic(EM)wave absorbers with wideband absorption capability are proposed as a strategy to mitigate environmental pollution by EM waves.However,designing an EM absorber with its performance capacity independent of the EM wave incident angle remains elusive to date.Resolving this challenge requires development of EM absorbers whose EM absorption performance is insensitive to the EM wave incident angle.Herein,we synthesized EM absorbers with a variety of structures with different symme-tries(including micro-/nanospheres,nanoflakes and nanotubes)to study the effect of the EM absorbers’structure and the EM wave incident angle on the EM absorption performance.Our analysis reveals that non-magnetic EM absorbers with spatially symmetric nanostructures exhibit excellent EM wave incident angle-insensitivity.Finally,we demonstrate that a class of non-magnetic EM absorbers made from bam-boo derived-carbon nanospheres exhibit EM incident angle-insensitivity and wideband EM absorption performance with an effective absorption band up to 3.5 GHz when the thickness is 1.4 mm,a signif-icant improvement from prior studies which used thicknesses as high as 3-4 mm for comparable EM absorption performance.
基金carried out in the framework of 3190/23/P and S/WZ/1/2015 works financed by Ministry of Science and Higher Education of Poland from the funds for science
文摘This study focuses on a CFD modelling of biomass-derived syngas co-firing with coal in an older mid-sized PC-fired boiler of type OP-230 with low-emission burners on the front wall. The simulations were performed to determine whether the boiler can be retrofitted for the fulfilment of the prospective environmental protection regulations relating to levels of NO_X emissions. The improvement of the air staging via the dual-fuel technique was based on the indirect co-firing technology. The impact of two arrangements of dedicated syngas nozzles(below and above the existing coal burners), two syngas compositions and two heat replacements(5% and 15%) on the course of thermal processes in a furnace was tested. The reductions in NO_X emissions were predicted relative to the baseline when only coal is combusted. The highest reduction of about 38% was achieved with the syngas nozzles below the existing coal burners and 15% heat replacement. This arrangement of nozzles offers the residence time sufficient to co-fire coal with waste derived syngas. A lower reduction in NO_X emissions was obtained with the nozzles above the burners as the enlargement of local fuel rich zone near syngas injection becomes significant for 15% heat replacement. Results provide for the decreasing impact of methane content along with the increase of syngas heat input. The avoided CO_2 emissions through the syngas indirect co-firing with coal in the boiler are linear function of heat replacements.