The pursuit of alternative fuel generation technologies has gained momentum due to the diminishing reserves of fossil fuels and global warming from increased CO_(2)emission.Among the proposed methods,the hydrogenation...The pursuit of alternative fuel generation technologies has gained momentum due to the diminishing reserves of fossil fuels and global warming from increased CO_(2)emission.Among the proposed methods,the hydrogenation of CO_(2)to produce marketable carbon-based products like methanol and ethanol is a practical approach that offers great potential to reduce CO_(2)emissions.Although significant volumes of methanol are currently produced from CO_(2),developing highly efficient and stable catalysts is crucial for further enhancing conversion and selectivity,thereby reducing process costs.An in-depth examination of the differences and similarities in the reaction pathways for methanol and ethanol production highlights the key factors that drive C-C coupling.Identifying these factors guides us toward developing more effective catalysts for ethanol synthesis.In this paper,we explore how different catalysts,through the production of various intermediates,can initiate the synthesis of methanol or ethanol.The catalytic mechanisms proposed by spectroscopic techniques and theoretical calculations,including operando X-ray methods,FTIR analysis,and DFT calculations,are summarized and presented.The following discussion explores the structural properties and composition of catalysts that influence C-C coupling and optimize the conversion rate of CO_(2)into ethanol.Lastly,the review examines recent catalysts employed for selective methanol and ethanol production,focusing on single-atom catalysts.展开更多
Direct ethanol fuel cells(DEFCs)are a promising alternative to conventional energy sources,offering high energy density,environmental sustainability,and operational safety.Compared to methanol fuel cells,DEFCs exhibit...Direct ethanol fuel cells(DEFCs)are a promising alternative to conventional energy sources,offering high energy density,environmental sustainability,and operational safety.Compared to methanol fuel cells,DEFCs exhibit lower toxicity and a more mature preparation process.Unlike hydrogen fuel cells,DEFCs provide superior storage and transport feasibility,as well as cost-effectiveness,significantly enhancing their commercial viability.However,the stable C-C bond in ethanol creates a high activation energy barrier,often resulting in incomplete electrooxidation.Current commercial platinum(Pt)-and palladium(Pd)-based catalysts demonstrate low C-C bond cleavage efficiency(<7.5%),severely limiting DEFC energy output and power density.Furthermore,high catalyst costs and insufficient activity impede large-scale commercialization.Recent advances in DEFC anode catalyst design have focused on optimizing material composition and elucidating catalytic mechanisms.This review systematically examines developments in ethanol electrooxidation catalysts over the past five years,highlighting strategies to improve C1 pathway selectivity and C-C bond activation.Key approaches,such as alloying,nanostructure engineering,and interfacial synergy effects,are discussed alongside their mechanistic implications.Finally,we outline current challenges and future prospects for DEFC commercialization.展开更多
Background:Despite the efficacy of absolute ethanol(EtOH),its radiolucency introduces several risks in interventional therapy for treating vascular malformations.This study aims to develop a novel radiopaque ethanol i...Background:Despite the efficacy of absolute ethanol(EtOH),its radiolucency introduces several risks in interventional therapy for treating vascular malformations.This study aims to develop a novel radiopaque ethanol injection(REI)to address this issue.Methods:Iopromide is mixed with ethanol to achieve radiopacity and improve the physicochemical properties of the solution.Overall,82 male New Zealand white rabbits are selected for in vivo radiopacity testing,peripheral vein sclerosis[animals were divided into the following 5 groups(n=6):negative control(NC,saline,0.250 ml/kg),positive control(EtOH,0.250 ml/kg),low-dose REI(L-D REI,0.125 ml/kg),moderate-dose REI(M-D REI,0.250 ml/kg),and highdose REI(H-D REI 0.375 ml/kg)],pharmacokinetic analyses(the blood sample was harvested before injection,5 min,10 min,20 min,40 min,1 h,2 h,4 h,and 8 h after injection in peripheral vein sclerosis experiment),peripheral artery embolization[animals were divided into the following 5 groups(n=3):NC(saline,0.250 ml/kg),positive control(EtOH,0.250 ml/kg),L-D REI(0.125 ml/kg),M-D REI(0.250 ml/kg),and H-D REI(0.375 ml/kg)],kidney transcatheter arterial embolization[animals were divided into the following 4 groups(n=3):positive control(EtOH,0.250 ml/kg),L-D REI(0.125 ml/kg),M-D REI(0.250 ml/kg),and H-D REI(0.375 ml/kg);each healthy kidney was injected with saline as negative control],and biosafety evaluations[animals were divided into the following 5 groups(n=3):NC(0.250 ml/kg),high-dose EtOH(0.375 ml/kg),L-D REI(0.125 ml/kg),M-D REI(0.250 ml/kg),and H-D REI(0.375 ml/kg)].Then,a prospective cohort study involving 6 patients with peripheral venous malformations(VMs)is performed to explore the clinical safety and effectiveness of REI.From Jun 1,2023 to August 31,2023,6 patients[age:(33.3±17.2)years]with lingual VMs received sclerotherapy of REI and 2-month follow-up.Adverse events and serious adverse events were evaluated,whereas the efficacy of REI was determined by both the traceability of the REI under DSA throughout the entire injection and the therapeutic effect 2 months after a single injection.Results:The REI contains 81.4%ethanol(v/v)and 111.3 mg/ml iodine,which can be traced throughout the injection in the animals and patients.The REI also exerts a similar effect as EtOH on peripheral venous sclerosis,peripheral arterial embolization,and renal embolization.Furthermore,the REI can be metabolized at a similar rate compared to EtOH and Ultravist^(®)and did not cause injury to the animals’heart,liver,spleen,lungs,kidneys and brain.No REIrelated adverse effects have occurred during sclerotherapy of VMs,and 4/6 patients(66.7%)have achieved complete response at follow-up.Conclusion:In conclusion,REI is safe,exerts therapeutic effects,and compensates for the radiolucency of EtOH in treating VMs.Trial registration:The clinical trial was registered as No.ChiCTR2300071751 on May 242023.展开更多
Highly active and stable electrocatalysts for ethanol oxidation reaction(EOR)are critical for the widespread adoption of direct ethanol fuel cells(DEFCs).However,the low efficiency of C–C bond cleavage of commercial ...Highly active and stable electrocatalysts for ethanol oxidation reaction(EOR)are critical for the widespread adoption of direct ethanol fuel cells(DEFCs).However,the low efficiency of C–C bond cleavage of commercial electrocatalysts not only leads to incomplete ethanol oxidation but also results in the accumulation of poisoning CO species.In this work,silver-platinum hollow nanocubes(AgPt hNCs)are designed and synthesized to achieve high selectivity for the complete 12-electron EOR in an alkaline electrolyte.AgPt h NCs demonstrate a Faradaic efficiency of up to 88.2%at the potential of 0.70 V for the C1 pathway and exhibit a 6.3-fold EOR mass activity than commercial Pt black at the potential of 0.81 V.Moreover,the oxyphilic nature of Ag imparts exceptional long-term stability to AgPt h NCs.Theoretical calculations reveal that the electronic interaction between Pt and Ag effectively modifies the d-band properties of surface Pt atoms,thereby optimizing the adsorption behavior of key intermediates,promoting the dehydrogenation of CH_(3)CO^(*)to CH_(2)CO^(*),and facilitating C–C bond cleavage.The present work provides both theoretical and experimental insights into the utilization of Ag-based alloy catalysts for highperformance DEFCs.展开更多
Substituting the sluggish oxygen evolution reaction with a more thermodynamically favorable ethanol oxidation reaction(EOR)offers an opportunity to circumvent the efficiency loss in water splitting and metal-air batte...Substituting the sluggish oxygen evolution reaction with a more thermodynamically favorable ethanol oxidation reaction(EOR)offers an opportunity to circumvent the efficiency loss in water splitting and metal-air batteries.However,the effect of the dynamic surface evolution of the catalyst in operating conditions on the activity of EOR lacks comprehensive understanding.Herein,we demonstrate a tunable operational catalyst activity through the modulated redox property of nickel oxalate(NCO)by establishing a relation between the oxidation behavior of Ni,surface reconstruction,and catalyst activity.We propose a repeated chemical-electrochemical reaction mechanism of EOR on NCO,which is rigorously investigated through a combination of operando Raman and nuclear magnetic resonance.The modulation of the oxidation trend of Ni by doping heteroatoms stimulates the electrochemical oxidation of the catalyst surface to NiOOH,which alters the catalyst activity for EOR.Assembled ethanol-assisted water electrolysis cell exhibits a reduced operating voltage for hydrogen production by 200 mV with a~100% Faradaic efficiency,and zinc-ethanol-air battery showed a 287 mV decreased charge-discharge voltage window and enhanced stability for over 500 h.展开更多
Alloying and interface effects are effective strategies for enhancing the performance of electrocatalysts in energy-related devices.Herein,dendritic Au-doped platinum-palladium alloy/dumbbell-like bismuth telluride he...Alloying and interface effects are effective strategies for enhancing the performance of electrocatalysts in energy-related devices.Herein,dendritic Au-doped platinum-palladium alloy/dumbbell-like bismuth telluride heterostructures(denoted PtPdAu/BiTe)were synthesized using a visible-light-assisted strategy.The coupling alloy and interfacial effects of PtPdAu/BiTe significantly improved the performance and stability of both the ethanol oxidation reaction(EOR)and methanol oxidation reaction(MOR).Introducing a small amount of Au effectively enhanced the CO tolerance of PtPdAu/BiTe compared to dendritic platinum-palladium alloy/dumbbell-like bismuth telluride heterostructures.PtPdAu/BiTe exhibited mass activities of 31.5 and 13.3 A·mg_(Pt)^(-1)in EOR and MOR,respectively,which were 34.4 and 13.2 times higher than those of commercial Pt black,revealing efficient Pt atom utilization.In-situ Fourier transform infrared spectroscopy demonstrated complete 12e^(-)and 6e^(-)oxidation of ethanol and methanol on PtPdAu/BiTe.The PtPdAu/BiTe/C achieved mass peak power densities of 131 and 156 mW·mg_(Pt)^(-1),which were 2.4 and 2.2 times higher than those of Pt/C in practical direct ethanol fuel cell(DEFC)and direct methanol fuel cell(DMFC),respectively,highlighting their potential application in DEFC and DMFC.This study introduces an effective strategy for designing efficient and highly CO tolerant anodic electrocatalysts for practical DEFC and DMFC applications.展开更多
Methane(CH4),the predominant component of natural gas and shale gas,is regarded as a promising carbon feedstock for chemical synthesis[1].However,considering the extreme stability of CH4 molecules,it's quite chall...Methane(CH4),the predominant component of natural gas and shale gas,is regarded as a promising carbon feedstock for chemical synthesis[1].However,considering the extreme stability of CH4 molecules,it's quite challenging in simultaneously achieving high activity and selectivity for target products under mild conditions,especially when synthesizing high-value C2t chemicals such as ethanol[2].The conversion of methane to ethanol by photocatalysis is promising for achieving transformation under ambient temperature and pressure conditions.Currently,the apparent quantum efficiency(AQE)of solar-driven methane-to-ethanol conversion is generally below 0.5%[3,4].Furthermore,the stability of photocatalysts remains inadequate,offering substantial potential for further improvement.展开更多
Our previous studies have reported that activation of the NLRP3(NOD-,LRR-and pyrin domain-containing protein 3)-inflammasome complex in ethanol-treated astrocytes and chronic alcohol-fed mice could be associated with ...Our previous studies have reported that activation of the NLRP3(NOD-,LRR-and pyrin domain-containing protein 3)-inflammasome complex in ethanol-treated astrocytes and chronic alcohol-fed mice could be associated with neuroinflammation and brain damage.Mesenchymal stem cell-derived extracellular vesicles(MSC-EVs)have been shown to restore the neuroinflammatory response,along with myelin and synaptic structural alterations in the prefrontal cortex,and alleviate cognitive and memory dysfunctions induced by binge-like ethanol treatment in adolescent mice.Considering the therapeutic role of the molecules contained in mesenchymal stem cell-derived extracellular vesicles,the present study analyzed whether the administration of mesenchymal stem cell-derived extracellular vesicles isolated from adipose tissue,which inhibited the activation of the NLRP3 inflammasome,was capable of reducing hippocampal neuroinflammation in adolescent mice treated with binge drinking.We demonstrated that the administration of mesenchymal stem cell-derived extracellular vesicles ameliorated the activation of the hippocampal NLRP3 inflammasome complex and other NLRs inflammasomes(e.g.,pyrin domain-containing 1,caspase recruitment domain-containing 4,and absent in melanoma 2,as well as the alterations in inflammatory genes(interleukin-1β,interleukin-18,inducible nitric oxide synthase,nuclear factor-kappa B,monocyte chemoattractant protein-1,and C–X3–C motif chemokine ligand 1)and miRNAs(miR-21a-5p,miR-146a-5p,and miR-141-5p)induced by binge-like ethanol treatment in adolescent mice.Bioinformatic analysis further revealed the involvement of miR-21a-5p and miR-146a-5p with inflammatory target genes and NOD-like receptor signaling pathways.Taken together,these findings provide novel evidence of the therapeutic potential of MSC-derived EVs to ameliorate the hippocampal neuroinflammatory response associated with NLRP3 inflammasome activation induced by binge drinking in adolescence.展开更多
Pt/Ni catalysts modified with CeO2 nanoparticles were prepared by simple composite electrodeposition of Ni and CeO2,and spontaneous Ni partial replacement by Pt processes.The as-prepared CeO2-modified Pt/Ni catalysts ...Pt/Ni catalysts modified with CeO2 nanoparticles were prepared by simple composite electrodeposition of Ni and CeO2,and spontaneous Ni partial replacement by Pt processes.The as-prepared CeO2-modified Pt/Ni catalysts showed enhanced catalytic performance for ethanol electro-oxidation compared with pure Pt/Ni,and acetate species were proposed to be the main products of the oxidation when using these catalysts.The content of CeO2 in the as-prepared catalysts influenced their catalytic activity,with Pt/NiCe2（obtained from an electrolyte containing 100 mg/L CeO2 nanoparticles） exhibiting higher activity and relatively better stability in ethanol electro-oxidation.This was mainly due to the oxygen storage capacity of CeO2,the interaction between Pt and CeO2/Ni,and the relatively small contact and charge transfer resistances.The results of this work thus suggest that electrocatalysts with low price and high activity can be rationally designed and produced by a simple route for use in direct ethanol fuel cells.展开更多
Molybdenum carbide has shown great potential in various hydrogenation reactions,and serves as a primary active species for synthesis of ethanol from dimethyl oxalate hydrogenation process which is a crucial step in th...Molybdenum carbide has shown great potential in various hydrogenation reactions,and serves as a primary active species for synthesis of ethanol from dimethyl oxalate hydrogenation process which is a crucial step in the efficient utilization of coal resources.In this study,a molybdenum carbide catalyst with a three-dimensional mesh-like hollow structure and lattice defects was carefully designed.The MoO_(3)precursor with abundant oxygen vacancies and defects was prepared by flame spray pyrolysis,and a structural modifier,Cu,was introduced by sputtering.The Cu deposited by sputtering affected the carburization and phase evolution processes.A three-dimensional mesh-like hollow structure composed of defective molybdenum carbide is formed,with theβ-Mo_(2)C exhibiting lattice distortions and defects.This defectiveβ-Mo_(2)C exhibits high reactivity,and facilitates the C=O hydrogenation process,showing a high reactivity of 83.1%yield in the hydrogenation of dimethyl oxalate.This work provides a new approach to the design and application of molybdenum carbide catalysts.展开更多
Agastache rugosa,a medicinal plant known for its bioactive compounds,has gained attention for its pharmacological and commercial potential.This study aimed to optimize ethanol concentration to enhance growth and bioac...Agastache rugosa,a medicinal plant known for its bioactive compounds,has gained attention for its pharmacological and commercial potential.This study aimed to optimize ethanol concentration to enhance growth and bioactive compound production in A.rugosa cultivated in a controlled plant factory system.Ethanol treatments at 40 and 80 mM significantly promoted both vegetative and reproductive growth.Plants treated with these concentrations exhibited higher net photosynthetic rates(A)and intercellular CO_(2) concentration(Ci)compared to the untreated control,whereas stomatal conductance(gs)and transpiration rate(E)remained unaffected.Chlorophyll and carotenoid concentrations,and SPAD values,significantly increased with ethanol treatment.Total flavonoid and total phenolic contents as well as 2,2-diphenyl-1-picrylhydrazyl(DPPH)radical-scavenging activities were significantly higher in plants treated with ethanol than in the untreated control.Ethanol treatments led to a significant enhancement in the activities of antioxidant enzymes,including superoxide dismutase,peroxidase,and catalase.Furthermore,ethanol treatment elevated rosmarinic acid concentrations in roots and tilianin and acacetin levels in flowers.Collectively,ethanol at 40 and 80 mM effectively enhanced growth,photosynthesis,antioxidant defense,and bioactive compound production in A.rugosa cultivated in a plant factory.These findings provide valuable insights for improving cultivation of medicinal plants with high pharmaceutical and nutraceutical value.展开更多
The catalytic synthesis of 1,3-butadiene(1,3-BD)from bio-based ethanol offers an alternative and sustainable process beyond petroleum.However,the intrinsic active sites and corresponding mechanism of 1,3-BD formation ...The catalytic synthesis of 1,3-butadiene(1,3-BD)from bio-based ethanol offers an alternative and sustainable process beyond petroleum.However,the intrinsic active sites and corresponding mechanism of 1,3-BD formation have not been fully elucidated yet.By correlating systematic characterization results with catalytic performance,the open Zr species,i.e.,Zr(OH)(OSi)_(3)moieties,were identified as the active site over the Zr/MFI-BM catalysts for the catalytic transformation of ethanol-acetaldehyde into 1,3-BD.In conjunction with controlled experiments and theory calculations,ethanol and acetaldehyde are proposed to synergistically co-adsorb on the Zr(OH)(OSi)_(3)species in a bi-molecular mode,which assists the acetaldehyde condensation and accelerates the critical Meerwein-Ponndorf-Verley-Oppenauer reduction,and accordingly promotes 1,3-BD formation.These findings will stimulate the search towards new metal-zeolite combinations for efficient production of value-added 1,3-BD via biomass-derived ethanol and beyond.展开更多
The aim of this study is to isolate and identify the chemical compounds in ethanol extract of Cyclocarya paliurus.Some purification and analysis techniques like silica gel,D101-macroporous adsorptive resins,and Sephad...The aim of this study is to isolate and identify the chemical compounds in ethanol extract of Cyclocarya paliurus.Some purification and analysis techniques like silica gel,D101-macroporous adsorptive resins,and Sephadex LH-20 column chromatographies as well as high-performance liquid chromatography were used to isolate and analyze the compounds from ethanol extract of Cyclocarya paliurus.The structures of these constituents were identified by spectroscopic techniques such as nuclear magnetic resonance and high-resolution mass spectrometries.Twenty-eight compounds,including flavonoids and their glycoside,carbohydrate,coumarin and organic acid,were isolated from ethyl acetate and n-butanol fractions in ethanol extract of Cyclocarya paliurus,and they were identified as kaempferol(1),coumestrol(2),kaempferol 3-O-β-D-glucoside(3),methyl caffeoylquinic acid(4),coptichic aldehyde(5),schizandriside(6),kaempferol 3-O-α-L-rhamnoside(7),3-caffeoylquinic acid ethyl ester(8),quercetin(9),luteolin(10),protocatechuic acid(11),kaempferol-3-O-α-L-furan arabinose(12),trans-p-hydroxy-cinnamic acid(13),α-D-glucopyranosido-β-D-fructofuranoside,sucrose(14),peucedanol(15),chlorogenic acid(16),pyridoxine(17),quercetin-3-O-β-D-glucuronide(18),kaempferol-3-O-β-D-glucuronide(19),isoquercitrin(20),mururin A(21),citroside A(22),benzyl-6-O-α-L-arabinofuranosyl-β-D-glucopyranoside(23),(+)-(6S,9R)-9-O-β-D-glucopyranosyl-6-hydroxy-3-O-α-ionol(24),myricetin-3-O-β-D-glucopyranoside(25),(4R)-4-(3-Oxo-1-buten-1-ylidene)-3α,5,5-trimethylcyclohexane-1α,3β-diol(26),quercetin-3-O-α-L-rhamnopyranosyl(27)and 3,5-O-dicaffeoylquinic acid(28).Compounds 2,5,6,15,21,22,23,24,26 and 28 were isolated from Cyclocarya paliurus for the first time.展开更多
Fuel injection properties,including the injection rate(temporal aspects)and spray behavior(spatial aspects),play a crucial role in the combustion efficiency and emissions of diesel engines.This study investigates the ...Fuel injection properties,including the injection rate(temporal aspects)and spray behavior(spatial aspects),play a crucial role in the combustion efficiency and emissions of diesel engines.This study investigates the effects of different ethanol-biodiesel-diesel(EBD)blends on the injection performance in diesel engines.Experimental tests are conducted to examine key injection parameters,such as spray penetration distance,spray cone angle,and droplet size,alongside an analysis of coupling leakage.The main findings are as follows:(1)The injection behavior of ethanol and diesel differs significantly.The addition of ethanol reduces the density,viscosity,and modulus of elasticity of the fuel mixture.While the injection advance angle,penetration distance,and Sauter mean diameter show minimal changes,the spray cone angle and coupling leakage increase notably.These alterations may disrupt the“fuelair-chamber”matching characteristics of the original engine,potentially affecting performance.(2)In contrast,the injection performance of biodiesel ismore similar to that of diesel.As biodiesel content increases,the density,viscosity,and modulus of elasticity of the blended fuel also grow.Though changes in injection timing,penetration distance,and spray cone angle remain minimal,the Sauter mean diameter experiences a slight increase.The“air-fuel chamber”compatibility of the original engine is largely unaffected,though fuel atomization slightly deteriorates.Blending up to 20%biodiesel and 30%ethanol with diesel effectively compensates for the shortcomings of using single fuels,maintaining favorable injection dynamics while enhancing lubrication and sealing performance of engine components.展开更多
Photocatalytic CO_(2)reduction to multi-carbon(C^(2+))products using solar energy is a promising route to carbon neutrality[1].Among these products,ethanol has attracted significant attention due to its high energy de...Photocatalytic CO_(2)reduction to multi-carbon(C^(2+))products using solar energy is a promising route to carbon neutrality[1].Among these products,ethanol has attracted significant attention due to its high energy density and convenient storage.However,achieving high selectivity for ethanol remains challenging because the reaction involves complex multi-electron transfer processes,and the ethanol pathway shares the same intermediate with the ethylene pathway,while the ethylene pathway has a thermodynamic advantage[2].This phenomenon makes it difficult to precisely control C-C coupling selectivity.展开更多
Alcohol abuse constitutes a significant health hazard,leading to various organ damage,notably the liver and brain.Shanxi aged vinegar(SAV)is one of the famous fermented and functional foods containing a variety of bio...Alcohol abuse constitutes a significant health hazard,leading to various organ damage,notably the liver and brain.Shanxi aged vinegar(SAV)is one of the famous fermented and functional foods containing a variety of bioactive ingredients with beneficial effects on the human body.This study aimed to explore the potential protective effect of SAV in alleviating acute alcohol intoxication(AAI)in mice.It was found that SAV at 2.5 mL/kg BW effectively ameliorated the decline in behavioral abilities following alcohol consumption,characterized by a shortened sobering period.SAV reduces alcohol-induced liver damage by inhibiting hepatic function enzymes and oxidative stress levels.Additionally,SAV mitigated the overactivation of microglia and the downregulation of neurotransmitter levels including acetylcholinesterase(AchE),5-hydroxytryptamine(5-HT)and dopamine(DA),thereby reducing ethanol-induced brain damage.Meanwhile,SAV significantly decreased concentrations of alcohol and acetaldehyde in the blood and increased alcohol dehydrogenase(ADH)and acetaldehyde dehydrogenase(ALDH)activities in the liver,indicating enhancement of ethanol metabolism.Moreover,we found that some gut microbiota including Verrucomicrobiota,Akkermansia,and Enterococcus were downregulated after SAV treatment in mice with AAI.These bacteria showed a negative correlation with anti-oxidative markers(glutathione(GSH)and catalase(CAT))and enzymes related to ethanol metabolism pathways(ADH and ALDH),and a positive correlation with hepatic function markers(alanine aminotransferase(ALT),aspartate aminotransferase(AST),and malondialdehyde(MDA)),alcohol metabolites(alcohol and acetaldehyde)and neurotransmitters(AchE,5-HT,and DA).However,Bacteroidota,norank_f_Muribaculaceae,and Alistipes exhibited the opposite direction.These findings suggest that SAV possesses protective effects against hepatic and neuro-toxicity,and could be a potential functional food for AAI prevention.展开更多
Extracting ethanol from aqueous solutions is important but challenging in industry.Pervaporation membranes show great promise for separating ethanol from water,with the design of their structure being crucial for enha...Extracting ethanol from aqueous solutions is important but challenging in industry.Pervaporation membranes show great promise for separating ethanol from water,with the design of their structure being crucial for enhancing performance.In this study,we developed an oriented bimetallic metal-organic framework(MOF)membrane,designated as ZIF-CoZn,for the pervaporation separation of ethanol from water.During crystal growth,bimetallic salts provide specific nucleation sites,and the competitive coordination between Co and Zn ions shifts the energetically favorable(100)plane to the(211)plane.This orientation enables precise molecular-level control over hydrophobic ligand arrangement,effectively repelling water molecules.Meanwhile,bimetallic competition enlarges pore sizes,facilitating ethanol permeation.When compared to single-metal MOF membranes made of cobalt or zinc,the separation factor of the ZIF-CoZn membrane for ethanol/water mixtures increased by 127%and 160%,respectively.Benefiting from the high roughness and increased exposure of hydrophobic ligands due to the preferential(211)orientation,ZIF-CoZn exhibits superhydrophobicity after vinyl-polydimethylsiloxane coating.The oriented ZIF-CoZn membrane was also scaled up to an area of 1 m^(2).This work provides valuable insights into optimizing MOF membrane structure and lays the foundation for its promotion and application in the industry.展开更多
Gold nanoparticles(AuNPs)supported on the Cu-doped LaMnO_(3)perovskites exhibit strong Au-Mn-Cu synergy in the aerobic oxidation of gaseous ethanol to acetaldehyde(AC).The Au/LaMnCuO_(3)catalysts achieve AC yields exc...Gold nanoparticles(AuNPs)supported on the Cu-doped LaMnO_(3)perovskites exhibit strong Au-Mn-Cu synergy in the aerobic oxidation of gaseous ethanol to acetaldehyde(AC).The Au/LaMnCuO_(3)catalysts achieve AC yields exceeding 90%and a space-time yield of 715 g_(AC)g_(AU)^(-1)h^(-1)at 225℃,outperforming reported catalysts.The outstanding performance is attributed to adjacent Cu^(+)and Mn^(2+)ions in the perovskite surface,which,together with nearby AuNPs,contribute to the high activity and stability.The best-performing catalyst contains a Cu/Mn ratio of 1/3 in the perovskite.Doping too much Cu into the perovskite leads to metallic Cu,suppressing catalyst performance.Density functional theory(reaction energetics,electronic structure analysis)and microkinetics simulations aided in understanding the synergy between Cu and Mn and the role of AuNPs.The reaction involves two H abstraction steps:(1)O-H cleavage of adsorbed ethanol by the basic perovskite lattice oxygen atom and(2)α-C-H cleavage by AuNPs,yielding AC and adsorbed water.Molecular O_(2)adsorbs in the oxygen vacancy(O_(V))formed by water removal,generating a peroxide anion(O_(2)^(2-))as the activated oxygen species.In the second part of the catalytic cycle,the basic O_(2)^(2-)species abstracts the H atom from another ethanol molecule,followed byα-C-H cleavage by AuNPs,AC production,and water removal.Water formation in the second part of the catalytic cycle is the rate-controlling step for Au/LaMnO_(3)and Au/LaMnCuO_(3)models.Moderate Cu doping enhances the essential Cu^(+)-OV-Mn^(2+)sites and lowers the barrier for water formation due to the weaker Cu-O bond than the Mn-O bond.In contrast,excessive Cu doping creates unstable Cu^(2+)-O-Cu^(2+)sites and shifts the barrier to theα-C-H cleavage.展开更多
Solution environment can influence the flexible structure of DNA under specific conditions,thereby affecting the stability of nucleic acids and ultimately impacting critical biological processes such as replication an...Solution environment can influence the flexible structure of DNA under specific conditions,thereby affecting the stability of nucleic acids and ultimately impacting critical biological processes such as replication and transcription.Intracellular solution environment is variable,and previous studies have demonstrated that it can enhance the stability of DNA structures under certain circumstances.In this work,molecular dynamics simulations were conducted on B-DNA(1ZEW,with a nucleotide sequence of CCTCTAGAGG)derived from human breast cancer cells(MDA-MB231)to explore the effects of ethanol solution on DNA configuration transformation at different temperatures and concentrations.The calculated results indicate that ethanol facilitates the transition of 1ZEW from B-DNA to A-DNA at lower temperature.Furthermore,it is observed that temperature affects DNA structure to some extent,thereby modifying the trend in DNA configuration transformation.At low temperatures,the ethanol can promote the transformation of B-DNA into A-DNA at higher concentrations.While at higher temperatures,the DNA could be in a state of thermal melting.These conclusions presented here can give valuable insights into how ethanol affects B-DNA configuration transformations.展开更多
Ethanol synthesis via dimethyl oxalate hydrogenation has garnered increasing attention in the fields of syngas utilization.Althoughε-Fe_(2)C has been identified as a promising active species for DMO hydrogenation to ...Ethanol synthesis via dimethyl oxalate hydrogenation has garnered increasing attention in the fields of syngas utilization.Althoughε-Fe_(2)C has been identified as a promising active species for DMO hydrogenation to ethanol,its formation is kinetically challenging during carbonization.In this work,a Fe_(4)N phase was first synthesized by pretreating a 30Fe/SiO_(2)catalyst in an ammonia environment,followed by carbonization in a methanol-H_(2) flow to obtain ε-Fe_(2)C as the active phase.Fe_(4)N,rather than Fe-O-Si,facilitates the transformation into iron carbide during the carbonization process.The transformation pathway of iron nitride(Fe_(x)N)is mediated by intermediate iron carbonyl species(Fe-CO),ultimately leading to the formation of iron carbide as the active phase.The resulting catalyst exhibited 40 times higher catalytic activity than the untreated catalyst in DMO hydrogenation.Combined structure properties and DFT calculation revealed that the lower energy barrier ofε-Fe_(2)C for ester hydrogenation underpins/strengthens its superior performance,while the STY of ε-Fe_(2)C is 2.8 times that ofε'-Fe_(2.2)C and 58 times that ofχ-Fe_(5)C_(2).This study provides a novel strategy for designing highly efficient iron carbide catalysts for the esters hydrogenation system.展开更多
基金the Canadian NRCan OERD Energy Innovation Programthe Natural Sciences and Engineering Research Council of Canada,and the Carbon Solution Program for their financial support.
文摘The pursuit of alternative fuel generation technologies has gained momentum due to the diminishing reserves of fossil fuels and global warming from increased CO_(2)emission.Among the proposed methods,the hydrogenation of CO_(2)to produce marketable carbon-based products like methanol and ethanol is a practical approach that offers great potential to reduce CO_(2)emissions.Although significant volumes of methanol are currently produced from CO_(2),developing highly efficient and stable catalysts is crucial for further enhancing conversion and selectivity,thereby reducing process costs.An in-depth examination of the differences and similarities in the reaction pathways for methanol and ethanol production highlights the key factors that drive C-C coupling.Identifying these factors guides us toward developing more effective catalysts for ethanol synthesis.In this paper,we explore how different catalysts,through the production of various intermediates,can initiate the synthesis of methanol or ethanol.The catalytic mechanisms proposed by spectroscopic techniques and theoretical calculations,including operando X-ray methods,FTIR analysis,and DFT calculations,are summarized and presented.The following discussion explores the structural properties and composition of catalysts that influence C-C coupling and optimize the conversion rate of CO_(2)into ethanol.Lastly,the review examines recent catalysts employed for selective methanol and ethanol production,focusing on single-atom catalysts.
基金supported by the National Natural Science Foundation of China(22472023,22202037)the Jilin Province Science and Technology Development Program(20250102077JC)the Fundamental Research Funds for the Central Universities(2412024QD014,2412023QD019).
文摘Direct ethanol fuel cells(DEFCs)are a promising alternative to conventional energy sources,offering high energy density,environmental sustainability,and operational safety.Compared to methanol fuel cells,DEFCs exhibit lower toxicity and a more mature preparation process.Unlike hydrogen fuel cells,DEFCs provide superior storage and transport feasibility,as well as cost-effectiveness,significantly enhancing their commercial viability.However,the stable C-C bond in ethanol creates a high activation energy barrier,often resulting in incomplete electrooxidation.Current commercial platinum(Pt)-and palladium(Pd)-based catalysts demonstrate low C-C bond cleavage efficiency(<7.5%),severely limiting DEFC energy output and power density.Furthermore,high catalyst costs and insufficient activity impede large-scale commercialization.Recent advances in DEFC anode catalyst design have focused on optimizing material composition and elucidating catalytic mechanisms.This review systematically examines developments in ethanol electrooxidation catalysts over the past five years,highlighting strategies to improve C1 pathway selectivity and C-C bond activation.Key approaches,such as alloying,nanostructure engineering,and interfacial synergy effects,are discussed alongside their mechanistic implications.Finally,we outline current challenges and future prospects for DEFC commercialization.
基金supported by the Transverse Research Project of Shanghai Ninth People’s Hospital(JYHX2022007)the Clinical Research Program of Ninth People’s Hospital,Shanghai Jiao Tong University School of Medicine(JYLJ202111).
文摘Background:Despite the efficacy of absolute ethanol(EtOH),its radiolucency introduces several risks in interventional therapy for treating vascular malformations.This study aims to develop a novel radiopaque ethanol injection(REI)to address this issue.Methods:Iopromide is mixed with ethanol to achieve radiopacity and improve the physicochemical properties of the solution.Overall,82 male New Zealand white rabbits are selected for in vivo radiopacity testing,peripheral vein sclerosis[animals were divided into the following 5 groups(n=6):negative control(NC,saline,0.250 ml/kg),positive control(EtOH,0.250 ml/kg),low-dose REI(L-D REI,0.125 ml/kg),moderate-dose REI(M-D REI,0.250 ml/kg),and highdose REI(H-D REI 0.375 ml/kg)],pharmacokinetic analyses(the blood sample was harvested before injection,5 min,10 min,20 min,40 min,1 h,2 h,4 h,and 8 h after injection in peripheral vein sclerosis experiment),peripheral artery embolization[animals were divided into the following 5 groups(n=3):NC(saline,0.250 ml/kg),positive control(EtOH,0.250 ml/kg),L-D REI(0.125 ml/kg),M-D REI(0.250 ml/kg),and H-D REI(0.375 ml/kg)],kidney transcatheter arterial embolization[animals were divided into the following 4 groups(n=3):positive control(EtOH,0.250 ml/kg),L-D REI(0.125 ml/kg),M-D REI(0.250 ml/kg),and H-D REI(0.375 ml/kg);each healthy kidney was injected with saline as negative control],and biosafety evaluations[animals were divided into the following 5 groups(n=3):NC(0.250 ml/kg),high-dose EtOH(0.375 ml/kg),L-D REI(0.125 ml/kg),M-D REI(0.250 ml/kg),and H-D REI(0.375 ml/kg)].Then,a prospective cohort study involving 6 patients with peripheral venous malformations(VMs)is performed to explore the clinical safety and effectiveness of REI.From Jun 1,2023 to August 31,2023,6 patients[age:(33.3±17.2)years]with lingual VMs received sclerotherapy of REI and 2-month follow-up.Adverse events and serious adverse events were evaluated,whereas the efficacy of REI was determined by both the traceability of the REI under DSA throughout the entire injection and the therapeutic effect 2 months after a single injection.Results:The REI contains 81.4%ethanol(v/v)and 111.3 mg/ml iodine,which can be traced throughout the injection in the animals and patients.The REI also exerts a similar effect as EtOH on peripheral venous sclerosis,peripheral arterial embolization,and renal embolization.Furthermore,the REI can be metabolized at a similar rate compared to EtOH and Ultravist^(®)and did not cause injury to the animals’heart,liver,spleen,lungs,kidneys and brain.No REIrelated adverse effects have occurred during sclerotherapy of VMs,and 4/6 patients(66.7%)have achieved complete response at follow-up.Conclusion:In conclusion,REI is safe,exerts therapeutic effects,and compensates for the radiolucency of EtOH in treating VMs.Trial registration:The clinical trial was registered as No.ChiCTR2300071751 on May 242023.
基金supported by the National Natural Science Foundation of China(22272103)the China Postdoctoral Science Foundation(2023TQ0204)+3 种基金the Fundamental Research Funds for the Central Universities(GK202304011)the Natural Science Foundation of Shaanxi Province(JC-YBQN-0088)the Science and Technology Innovation Team of Shaanxi Province(2023-CX-TD-27)the Sanqin scholars innovation teams in Shaanxi Province,China。
文摘Highly active and stable electrocatalysts for ethanol oxidation reaction(EOR)are critical for the widespread adoption of direct ethanol fuel cells(DEFCs).However,the low efficiency of C–C bond cleavage of commercial electrocatalysts not only leads to incomplete ethanol oxidation but also results in the accumulation of poisoning CO species.In this work,silver-platinum hollow nanocubes(AgPt hNCs)are designed and synthesized to achieve high selectivity for the complete 12-electron EOR in an alkaline electrolyte.AgPt h NCs demonstrate a Faradaic efficiency of up to 88.2%at the potential of 0.70 V for the C1 pathway and exhibit a 6.3-fold EOR mass activity than commercial Pt black at the potential of 0.81 V.Moreover,the oxyphilic nature of Ag imparts exceptional long-term stability to AgPt h NCs.Theoretical calculations reveal that the electronic interaction between Pt and Ag effectively modifies the d-band properties of surface Pt atoms,thereby optimizing the adsorption behavior of key intermediates,promoting the dehydrogenation of CH_(3)CO^(*)to CH_(2)CO^(*),and facilitating C–C bond cleavage.The present work provides both theoretical and experimental insights into the utilization of Ag-based alloy catalysts for highperformance DEFCs.
基金supported by the National Research Foundation of Korea(NRF)funded by Ministry of Science and ICT(NRF-2022M3H4A1A04076616 and NRF-2022M3H4A1A01008918)a cooperation project of“Basic project(referring to projects performed with the budget directly contributed by the Government to achieve the purposes of establishment of Government–funded research Institutes)”supported by the Korea Research Institute of Chemical Technology(KRICT).
文摘Substituting the sluggish oxygen evolution reaction with a more thermodynamically favorable ethanol oxidation reaction(EOR)offers an opportunity to circumvent the efficiency loss in water splitting and metal-air batteries.However,the effect of the dynamic surface evolution of the catalyst in operating conditions on the activity of EOR lacks comprehensive understanding.Herein,we demonstrate a tunable operational catalyst activity through the modulated redox property of nickel oxalate(NCO)by establishing a relation between the oxidation behavior of Ni,surface reconstruction,and catalyst activity.We propose a repeated chemical-electrochemical reaction mechanism of EOR on NCO,which is rigorously investigated through a combination of operando Raman and nuclear magnetic resonance.The modulation of the oxidation trend of Ni by doping heteroatoms stimulates the electrochemical oxidation of the catalyst surface to NiOOH,which alters the catalyst activity for EOR.Assembled ethanol-assisted water electrolysis cell exhibits a reduced operating voltage for hydrogen production by 200 mV with a~100% Faradaic efficiency,and zinc-ethanol-air battery showed a 287 mV decreased charge-discharge voltage window and enhanced stability for over 500 h.
基金supported by the National Natural Science Foundation of China(No.22465009)the Education Department of Guizhou Province(No.2021312)the Foundation of Guizhou Province(No.2019-5666).
文摘Alloying and interface effects are effective strategies for enhancing the performance of electrocatalysts in energy-related devices.Herein,dendritic Au-doped platinum-palladium alloy/dumbbell-like bismuth telluride heterostructures(denoted PtPdAu/BiTe)were synthesized using a visible-light-assisted strategy.The coupling alloy and interfacial effects of PtPdAu/BiTe significantly improved the performance and stability of both the ethanol oxidation reaction(EOR)and methanol oxidation reaction(MOR).Introducing a small amount of Au effectively enhanced the CO tolerance of PtPdAu/BiTe compared to dendritic platinum-palladium alloy/dumbbell-like bismuth telluride heterostructures.PtPdAu/BiTe exhibited mass activities of 31.5 and 13.3 A·mg_(Pt)^(-1)in EOR and MOR,respectively,which were 34.4 and 13.2 times higher than those of commercial Pt black,revealing efficient Pt atom utilization.In-situ Fourier transform infrared spectroscopy demonstrated complete 12e^(-)and 6e^(-)oxidation of ethanol and methanol on PtPdAu/BiTe.The PtPdAu/BiTe/C achieved mass peak power densities of 131 and 156 mW·mg_(Pt)^(-1),which were 2.4 and 2.2 times higher than those of Pt/C in practical direct ethanol fuel cell(DEFC)and direct methanol fuel cell(DMFC),respectively,highlighting their potential application in DEFC and DMFC.This study introduces an effective strategy for designing efficient and highly CO tolerant anodic electrocatalysts for practical DEFC and DMFC applications.
基金the support from the National Natural Science Foundation of China(52202306)Program from Guangdong Introducing Innovative and Entrepreneurial Teams(2019ZT08L101 and RCTDPT-2020-001)+1 种基金Shenzhen Key Laboratory of Eco-materials and Renewable Energy(ZDSYS20200922160400001)the Provincial Talent Plan of Guangdong(2023TB0012).
文摘Methane(CH4),the predominant component of natural gas and shale gas,is regarded as a promising carbon feedstock for chemical synthesis[1].However,considering the extreme stability of CH4 molecules,it's quite challenging in simultaneously achieving high activity and selectivity for target products under mild conditions,especially when synthesizing high-value C2t chemicals such as ethanol[2].The conversion of methane to ethanol by photocatalysis is promising for achieving transformation under ambient temperature and pressure conditions.Currently,the apparent quantum efficiency(AQE)of solar-driven methane-to-ethanol conversion is generally below 0.5%[3,4].Furthermore,the stability of photocatalysts remains inadequate,offering substantial potential for further improvement.
基金supported by grants from the Spanish Ministry of Health-PNSD(2019-I039 and 2023-I024)(to MP)FEDER/Ministerio de Ciencia e Innovación-Agencia Estatal de Investigación PID2021-1243590B-I100(to VMM)+2 种基金GVA(CIAICO/2021/203)(to MP)the Primary Addiction Care Research Network(RD21/0009/0005)(to MP)a predoctoral fellowship from the Generalitat Valenciana(ACIF/2021/338)(to CPC).
文摘Our previous studies have reported that activation of the NLRP3(NOD-,LRR-and pyrin domain-containing protein 3)-inflammasome complex in ethanol-treated astrocytes and chronic alcohol-fed mice could be associated with neuroinflammation and brain damage.Mesenchymal stem cell-derived extracellular vesicles(MSC-EVs)have been shown to restore the neuroinflammatory response,along with myelin and synaptic structural alterations in the prefrontal cortex,and alleviate cognitive and memory dysfunctions induced by binge-like ethanol treatment in adolescent mice.Considering the therapeutic role of the molecules contained in mesenchymal stem cell-derived extracellular vesicles,the present study analyzed whether the administration of mesenchymal stem cell-derived extracellular vesicles isolated from adipose tissue,which inhibited the activation of the NLRP3 inflammasome,was capable of reducing hippocampal neuroinflammation in adolescent mice treated with binge drinking.We demonstrated that the administration of mesenchymal stem cell-derived extracellular vesicles ameliorated the activation of the hippocampal NLRP3 inflammasome complex and other NLRs inflammasomes(e.g.,pyrin domain-containing 1,caspase recruitment domain-containing 4,and absent in melanoma 2,as well as the alterations in inflammatory genes(interleukin-1β,interleukin-18,inducible nitric oxide synthase,nuclear factor-kappa B,monocyte chemoattractant protein-1,and C–X3–C motif chemokine ligand 1)and miRNAs(miR-21a-5p,miR-146a-5p,and miR-141-5p)induced by binge-like ethanol treatment in adolescent mice.Bioinformatic analysis further revealed the involvement of miR-21a-5p and miR-146a-5p with inflammatory target genes and NOD-like receptor signaling pathways.Taken together,these findings provide novel evidence of the therapeutic potential of MSC-derived EVs to ameliorate the hippocampal neuroinflammatory response associated with NLRP3 inflammasome activation induced by binge drinking in adolescence.
基金supported by the National Natural Science Foundation of China (21307038 and 21577046)Key Project of Chinese Ministry of Education (212115)Physical Chemistry Experiment of Huanggang Normal University (2015CK12)~~
文摘Pt/Ni catalysts modified with CeO2 nanoparticles were prepared by simple composite electrodeposition of Ni and CeO2,and spontaneous Ni partial replacement by Pt processes.The as-prepared CeO2-modified Pt/Ni catalysts showed enhanced catalytic performance for ethanol electro-oxidation compared with pure Pt/Ni,and acetate species were proposed to be the main products of the oxidation when using these catalysts.The content of CeO2 in the as-prepared catalysts influenced their catalytic activity,with Pt/NiCe2（obtained from an electrolyte containing 100 mg/L CeO2 nanoparticles） exhibiting higher activity and relatively better stability in ethanol electro-oxidation.This was mainly due to the oxygen storage capacity of CeO2,the interaction between Pt and CeO2/Ni,and the relatively small contact and charge transfer resistances.The results of this work thus suggest that electrocatalysts with low price and high activity can be rationally designed and produced by a simple route for use in direct ethanol fuel cells.
文摘Molybdenum carbide has shown great potential in various hydrogenation reactions,and serves as a primary active species for synthesis of ethanol from dimethyl oxalate hydrogenation process which is a crucial step in the efficient utilization of coal resources.In this study,a molybdenum carbide catalyst with a three-dimensional mesh-like hollow structure and lattice defects was carefully designed.The MoO_(3)precursor with abundant oxygen vacancies and defects was prepared by flame spray pyrolysis,and a structural modifier,Cu,was introduced by sputtering.The Cu deposited by sputtering affected the carburization and phase evolution processes.A three-dimensional mesh-like hollow structure composed of defective molybdenum carbide is formed,with theβ-Mo_(2)C exhibiting lattice distortions and defects.This defectiveβ-Mo_(2)C exhibits high reactivity,and facilitates the C=O hydrogenation process,showing a high reactivity of 83.1%yield in the hydrogenation of dimethyl oxalate.This work provides a new approach to the design and application of molybdenum carbide catalysts.
基金supported by Korea Institute of Energy Technology Evaluation and Planning(KETEP)grant funded by the Korea government(MOTIE)(20212020800050,Development and demonstration of rooftop greenhouse-building integrated system using distributed polygeneration).
文摘Agastache rugosa,a medicinal plant known for its bioactive compounds,has gained attention for its pharmacological and commercial potential.This study aimed to optimize ethanol concentration to enhance growth and bioactive compound production in A.rugosa cultivated in a controlled plant factory system.Ethanol treatments at 40 and 80 mM significantly promoted both vegetative and reproductive growth.Plants treated with these concentrations exhibited higher net photosynthetic rates(A)and intercellular CO_(2) concentration(Ci)compared to the untreated control,whereas stomatal conductance(gs)and transpiration rate(E)remained unaffected.Chlorophyll and carotenoid concentrations,and SPAD values,significantly increased with ethanol treatment.Total flavonoid and total phenolic contents as well as 2,2-diphenyl-1-picrylhydrazyl(DPPH)radical-scavenging activities were significantly higher in plants treated with ethanol than in the untreated control.Ethanol treatments led to a significant enhancement in the activities of antioxidant enzymes,including superoxide dismutase,peroxidase,and catalase.Furthermore,ethanol treatment elevated rosmarinic acid concentrations in roots and tilianin and acacetin levels in flowers.Collectively,ethanol at 40 and 80 mM effectively enhanced growth,photosynthesis,antioxidant defense,and bioactive compound production in A.rugosa cultivated in a plant factory.These findings provide valuable insights for improving cultivation of medicinal plants with high pharmaceutical and nutraceutical value.
文摘The catalytic synthesis of 1,3-butadiene(1,3-BD)from bio-based ethanol offers an alternative and sustainable process beyond petroleum.However,the intrinsic active sites and corresponding mechanism of 1,3-BD formation have not been fully elucidated yet.By correlating systematic characterization results with catalytic performance,the open Zr species,i.e.,Zr(OH)(OSi)_(3)moieties,were identified as the active site over the Zr/MFI-BM catalysts for the catalytic transformation of ethanol-acetaldehyde into 1,3-BD.In conjunction with controlled experiments and theory calculations,ethanol and acetaldehyde are proposed to synergistically co-adsorb on the Zr(OH)(OSi)_(3)species in a bi-molecular mode,which assists the acetaldehyde condensation and accelerates the critical Meerwein-Ponndorf-Verley-Oppenauer reduction,and accordingly promotes 1,3-BD formation.These findings will stimulate the search towards new metal-zeolite combinations for efficient production of value-added 1,3-BD via biomass-derived ethanol and beyond.
文摘The aim of this study is to isolate and identify the chemical compounds in ethanol extract of Cyclocarya paliurus.Some purification and analysis techniques like silica gel,D101-macroporous adsorptive resins,and Sephadex LH-20 column chromatographies as well as high-performance liquid chromatography were used to isolate and analyze the compounds from ethanol extract of Cyclocarya paliurus.The structures of these constituents were identified by spectroscopic techniques such as nuclear magnetic resonance and high-resolution mass spectrometries.Twenty-eight compounds,including flavonoids and their glycoside,carbohydrate,coumarin and organic acid,were isolated from ethyl acetate and n-butanol fractions in ethanol extract of Cyclocarya paliurus,and they were identified as kaempferol(1),coumestrol(2),kaempferol 3-O-β-D-glucoside(3),methyl caffeoylquinic acid(4),coptichic aldehyde(5),schizandriside(6),kaempferol 3-O-α-L-rhamnoside(7),3-caffeoylquinic acid ethyl ester(8),quercetin(9),luteolin(10),protocatechuic acid(11),kaempferol-3-O-α-L-furan arabinose(12),trans-p-hydroxy-cinnamic acid(13),α-D-glucopyranosido-β-D-fructofuranoside,sucrose(14),peucedanol(15),chlorogenic acid(16),pyridoxine(17),quercetin-3-O-β-D-glucuronide(18),kaempferol-3-O-β-D-glucuronide(19),isoquercitrin(20),mururin A(21),citroside A(22),benzyl-6-O-α-L-arabinofuranosyl-β-D-glucopyranoside(23),(+)-(6S,9R)-9-O-β-D-glucopyranosyl-6-hydroxy-3-O-α-ionol(24),myricetin-3-O-β-D-glucopyranoside(25),(4R)-4-(3-Oxo-1-buten-1-ylidene)-3α,5,5-trimethylcyclohexane-1α,3β-diol(26),quercetin-3-O-α-L-rhamnopyranosyl(27)and 3,5-O-dicaffeoylquinic acid(28).Compounds 2,5,6,15,21,22,23,24,26 and 28 were isolated from Cyclocarya paliurus for the first time.
基金supported by Innovation Research Project for the training of high-level scientific and technological talents(Technical expert talents)of the Armed Police Force ZZKY20222415“13th Five-Year Plan”military key colleges and key disciplines-Equipment Engineering(Power)-17.
文摘Fuel injection properties,including the injection rate(temporal aspects)and spray behavior(spatial aspects),play a crucial role in the combustion efficiency and emissions of diesel engines.This study investigates the effects of different ethanol-biodiesel-diesel(EBD)blends on the injection performance in diesel engines.Experimental tests are conducted to examine key injection parameters,such as spray penetration distance,spray cone angle,and droplet size,alongside an analysis of coupling leakage.The main findings are as follows:(1)The injection behavior of ethanol and diesel differs significantly.The addition of ethanol reduces the density,viscosity,and modulus of elasticity of the fuel mixture.While the injection advance angle,penetration distance,and Sauter mean diameter show minimal changes,the spray cone angle and coupling leakage increase notably.These alterations may disrupt the“fuelair-chamber”matching characteristics of the original engine,potentially affecting performance.(2)In contrast,the injection performance of biodiesel ismore similar to that of diesel.As biodiesel content increases,the density,viscosity,and modulus of elasticity of the blended fuel also grow.Though changes in injection timing,penetration distance,and spray cone angle remain minimal,the Sauter mean diameter experiences a slight increase.The“air-fuel chamber”compatibility of the original engine is largely unaffected,though fuel atomization slightly deteriorates.Blending up to 20%biodiesel and 30%ethanol with diesel effectively compensates for the shortcomings of using single fuels,maintaining favorable injection dynamics while enhancing lubrication and sealing performance of engine components.
基金supported by National Natural Science Foundation of China(Nos.52473327,51572295 and 21273285)National Key R&D Program of China(Nos.2021YFA1501300,2019YFC1907602).
文摘Photocatalytic CO_(2)reduction to multi-carbon(C^(2+))products using solar energy is a promising route to carbon neutrality[1].Among these products,ethanol has attracted significant attention due to its high energy density and convenient storage.However,achieving high selectivity for ethanol remains challenging because the reaction involves complex multi-electron transfer processes,and the ethanol pathway shares the same intermediate with the ethylene pathway,while the ethylene pathway has a thermodynamic advantage[2].This phenomenon makes it difficult to precisely control C-C coupling selectivity.
基金financially supported by the Natural Science Foundation of Tianjin(24JCYBJC01220)the Open Project Program of State Key Laboratory of Food Nutrition and Safety,Tianjin University of Science&Technology(SKLFNS-NF-202318)the foundation of Shanxi Provincial Key Laboratory for Vinegar Fermentation Science and Engineering,China(20220401931002).
文摘Alcohol abuse constitutes a significant health hazard,leading to various organ damage,notably the liver and brain.Shanxi aged vinegar(SAV)is one of the famous fermented and functional foods containing a variety of bioactive ingredients with beneficial effects on the human body.This study aimed to explore the potential protective effect of SAV in alleviating acute alcohol intoxication(AAI)in mice.It was found that SAV at 2.5 mL/kg BW effectively ameliorated the decline in behavioral abilities following alcohol consumption,characterized by a shortened sobering period.SAV reduces alcohol-induced liver damage by inhibiting hepatic function enzymes and oxidative stress levels.Additionally,SAV mitigated the overactivation of microglia and the downregulation of neurotransmitter levels including acetylcholinesterase(AchE),5-hydroxytryptamine(5-HT)and dopamine(DA),thereby reducing ethanol-induced brain damage.Meanwhile,SAV significantly decreased concentrations of alcohol and acetaldehyde in the blood and increased alcohol dehydrogenase(ADH)and acetaldehyde dehydrogenase(ALDH)activities in the liver,indicating enhancement of ethanol metabolism.Moreover,we found that some gut microbiota including Verrucomicrobiota,Akkermansia,and Enterococcus were downregulated after SAV treatment in mice with AAI.These bacteria showed a negative correlation with anti-oxidative markers(glutathione(GSH)and catalase(CAT))and enzymes related to ethanol metabolism pathways(ADH and ALDH),and a positive correlation with hepatic function markers(alanine aminotransferase(ALT),aspartate aminotransferase(AST),and malondialdehyde(MDA)),alcohol metabolites(alcohol and acetaldehyde)and neurotransmitters(AchE,5-HT,and DA).However,Bacteroidota,norank_f_Muribaculaceae,and Alistipes exhibited the opposite direction.These findings suggest that SAV possesses protective effects against hepatic and neuro-toxicity,and could be a potential functional food for AAI prevention.
基金the funding from the National Key Research and Development Program of China(No.2022YFB3804802)the National Natural Science Foundation of China(22125801,22478012)Beijing Natural Science Foundation(Z230023)。
文摘Extracting ethanol from aqueous solutions is important but challenging in industry.Pervaporation membranes show great promise for separating ethanol from water,with the design of their structure being crucial for enhancing performance.In this study,we developed an oriented bimetallic metal-organic framework(MOF)membrane,designated as ZIF-CoZn,for the pervaporation separation of ethanol from water.During crystal growth,bimetallic salts provide specific nucleation sites,and the competitive coordination between Co and Zn ions shifts the energetically favorable(100)plane to the(211)plane.This orientation enables precise molecular-level control over hydrophobic ligand arrangement,effectively repelling water molecules.Meanwhile,bimetallic competition enlarges pore sizes,facilitating ethanol permeation.When compared to single-metal MOF membranes made of cobalt or zinc,the separation factor of the ZIF-CoZn membrane for ethanol/water mixtures increased by 127%and 160%,respectively.Benefiting from the high roughness and increased exposure of hydrophobic ligands due to the preferential(211)orientation,ZIF-CoZn exhibits superhydrophobicity after vinyl-polydimethylsiloxane coating.The oriented ZIF-CoZn membrane was also scaled up to an area of 1 m^(2).This work provides valuable insights into optimizing MOF membrane structure and lays the foundation for its promotion and application in the industry.
文摘Gold nanoparticles(AuNPs)supported on the Cu-doped LaMnO_(3)perovskites exhibit strong Au-Mn-Cu synergy in the aerobic oxidation of gaseous ethanol to acetaldehyde(AC).The Au/LaMnCuO_(3)catalysts achieve AC yields exceeding 90%and a space-time yield of 715 g_(AC)g_(AU)^(-1)h^(-1)at 225℃,outperforming reported catalysts.The outstanding performance is attributed to adjacent Cu^(+)and Mn^(2+)ions in the perovskite surface,which,together with nearby AuNPs,contribute to the high activity and stability.The best-performing catalyst contains a Cu/Mn ratio of 1/3 in the perovskite.Doping too much Cu into the perovskite leads to metallic Cu,suppressing catalyst performance.Density functional theory(reaction energetics,electronic structure analysis)and microkinetics simulations aided in understanding the synergy between Cu and Mn and the role of AuNPs.The reaction involves two H abstraction steps:(1)O-H cleavage of adsorbed ethanol by the basic perovskite lattice oxygen atom and(2)α-C-H cleavage by AuNPs,yielding AC and adsorbed water.Molecular O_(2)adsorbs in the oxygen vacancy(O_(V))formed by water removal,generating a peroxide anion(O_(2)^(2-))as the activated oxygen species.In the second part of the catalytic cycle,the basic O_(2)^(2-)species abstracts the H atom from another ethanol molecule,followed byα-C-H cleavage by AuNPs,AC production,and water removal.Water formation in the second part of the catalytic cycle is the rate-controlling step for Au/LaMnO_(3)and Au/LaMnCuO_(3)models.Moderate Cu doping enhances the essential Cu^(+)-OV-Mn^(2+)sites and lowers the barrier for water formation due to the weaker Cu-O bond than the Mn-O bond.In contrast,excessive Cu doping creates unstable Cu^(2+)-O-Cu^(2+)sites and shifts the barrier to theα-C-H cleavage.
基金supported by the National Natural Science Foun-dation of China(Grant Nos.52073128 and 11964012)the Foundation of Educational Committee of Jiangxi Province of China(Grant No.GJJ2201314).
文摘Solution environment can influence the flexible structure of DNA under specific conditions,thereby affecting the stability of nucleic acids and ultimately impacting critical biological processes such as replication and transcription.Intracellular solution environment is variable,and previous studies have demonstrated that it can enhance the stability of DNA structures under certain circumstances.In this work,molecular dynamics simulations were conducted on B-DNA(1ZEW,with a nucleotide sequence of CCTCTAGAGG)derived from human breast cancer cells(MDA-MB231)to explore the effects of ethanol solution on DNA configuration transformation at different temperatures and concentrations.The calculated results indicate that ethanol facilitates the transition of 1ZEW from B-DNA to A-DNA at lower temperature.Furthermore,it is observed that temperature affects DNA structure to some extent,thereby modifying the trend in DNA configuration transformation.At low temperatures,the ethanol can promote the transformation of B-DNA into A-DNA at higher concentrations.While at higher temperatures,the DNA could be in a state of thermal melting.These conclusions presented here can give valuable insights into how ethanol affects B-DNA configuration transformations.
基金supported by the National Natural Science Foundation of China(21878227,22278309)。
文摘Ethanol synthesis via dimethyl oxalate hydrogenation has garnered increasing attention in the fields of syngas utilization.Althoughε-Fe_(2)C has been identified as a promising active species for DMO hydrogenation to ethanol,its formation is kinetically challenging during carbonization.In this work,a Fe_(4)N phase was first synthesized by pretreating a 30Fe/SiO_(2)catalyst in an ammonia environment,followed by carbonization in a methanol-H_(2) flow to obtain ε-Fe_(2)C as the active phase.Fe_(4)N,rather than Fe-O-Si,facilitates the transformation into iron carbide during the carbonization process.The transformation pathway of iron nitride(Fe_(x)N)is mediated by intermediate iron carbonyl species(Fe-CO),ultimately leading to the formation of iron carbide as the active phase.The resulting catalyst exhibited 40 times higher catalytic activity than the untreated catalyst in DMO hydrogenation.Combined structure properties and DFT calculation revealed that the lower energy barrier ofε-Fe_(2)C for ester hydrogenation underpins/strengthens its superior performance,while the STY of ε-Fe_(2)C is 2.8 times that ofε'-Fe_(2.2)C and 58 times that ofχ-Fe_(5)C_(2).This study provides a novel strategy for designing highly efficient iron carbide catalysts for the esters hydrogenation system.
