Lithium iron phosphate(LFP)has found many applications in the field of electric vehicles and energy storage systems.However,the increasing volume of end-of-life LFP batteries poses an urgent challenge in terms of envi...Lithium iron phosphate(LFP)has found many applications in the field of electric vehicles and energy storage systems.However,the increasing volume of end-of-life LFP batteries poses an urgent challenge in terms of environmental sustainability and resource management.Therefore,the development and implementation of efficient LFP battery recycling methods are crucial to address these challenges.This article presents a novel,comprehensive evaluation framework for comparing different lithium iron phosphate relithiation techniques.The framework includes three main sets of criteria:direct production cost,electrochemical performance,and environmental impact.Each criterion is scored on a scale of 0–100,with higher scores indicating better performance.The direct production cost is rated based on material costs,energy consumption,key equipment costs,process duration and space requirements.Electrochemical performance is assessed by rate capability and cycle stability.Environmental impact is assessed based on CO_(2)emissions.The framework provides a standardized technique for researchers and industry professionals to objectively compare relithiation methods,facilitating the identification of the most promising approaches for further development and scale-up.The total average score across the three criterion groups for electrochemical,chemical,and hydrothermal relithiation methods was approximately 60 points,while sintering scored 39 points,making it the least attractive relithiation technique.Combining approaches outlined in publications with scores exceeding 60,a relithiation scheme was proposed to achieve optimal electrochemical performance with minimal resource consumption and environmental impact.The results demonstrate the framework’s applicability and highlight areas for future research and optimization in lithium iron phosphate cathode recycling.展开更多
Effective utilization of hot electrons generated from the decay of surface plasmon resonance in metal nanoparticles is conductive to improve solar water splitting efficiency.Herein,Ag nanoparticles and reduced graphen...Effective utilization of hot electrons generated from the decay of surface plasmon resonance in metal nanoparticles is conductive to improve solar water splitting efficiency.Herein,Ag nanoparticles and reduced graphene oxide(rGO)co-decorated hierarchical TiO2 nanoring/nanotube arrays(TiO2 R/T)were facilely fabricated by using two-step electrochemical anodization,electrodeposition,and photoreduction methods.Comparative studies were conducted to elucidate the effects of rGO and Ag on the morphology,photoresponse,charge transfer,and photoelectric properties of TiO2.Firstly,scanning electron microscope images confirm that the Ag nanoparticles adhered on TiO2 R/T and TiO2 R/T-rGO have similar diameter of 20 nm except for TiO2 R-rGO/T.Then,the UV-Vis DRS and scatter spectra reveal that the optical property of the Ag-TiO2 R/T-rGO ternary composite is enhanced,ascribing to the visible light absorption of plasmonic Ag nanoparticles and the weakening effect of rGO on light scattering.Meanwhile,intensity-modulated photocurrent spectroscopy and photoluminescence spectra demonstrate that rGO can promote the hot electrons transfer from Ag nanoparticles to Ti substrate,reducing the photogenerated electron-hole recombination.Finally,Ag-TiO2 R/T-rGO photoanode exhibits high photocurrent density(0.98 mA cm?2)and photovoltage(0.90 V),and the stable H2 evolution rate of 413μL h?1 cm?2 within 1.5 h under AM 1.5 which exceeds by 1.30 times than that of pristine TiO2 R/T.In line with the above results,this work provides a reliable route synergizing rGO with plasmonic metal nanoparticles for photocatalysis,in which,rGO presents a broad absorption spectrum and effective photogenerated electrons transfer.展开更多
Gluconic acid and its derivatives have been widely used in the food and pharmaceutical industries. Conventional processes that involve the conversion of glucose into gluconic acid via fermentation present several tech...Gluconic acid and its derivatives have been widely used in the food and pharmaceutical industries. Conventional processes that involve the conversion of glucose into gluconic acid via fermentation present several technological shortcomings as they involve energy-intensive wastewater treatment and complex enzyme separation. Greener oxidation processes over heterogeneous metal catalysts have attracted increasing attention worldwide. Au-, Pt-and Pd-based heterogeneous catalysts have been extensively used for the chemical oxidation of glucose to gluconic acid. Bimetallic catalysts synthesized by adding either noble or inexpensive metals have also presented excellent performance for the oxidations of glucose. In particular, particle size, which has been recognized as the most important factor that affect catalytic performances, could be rationally tuned by changing the types of support and ligand as well as the synthesis conditions. In this perspective review, we summarize and critically discuss the recent advances in the structural design of mono-and bimetallic catalysts for the oxidation of glucose in aqueous media. Furthermore, the challenges of developing catalysts for the green synthesis of gluconic acid have been highlighted. This review provides alternative insights for designing effective catalytic materials for the catalytic oxidation of bio-derived oxygenates over heterogeneous catalysts.展开更多
LiNi_(0.8)Co_(0.15)Al_(0.05)O_(2)(NCA) is a promising cathode for sulfide-based solid-state lithium batteries(ASSLBs)profiting from its high specific capacity and voltage plateau, which yielding high energy density. H...LiNi_(0.8)Co_(0.15)Al_(0.05)O_(2)(NCA) is a promising cathode for sulfide-based solid-state lithium batteries(ASSLBs)profiting from its high specific capacity and voltage plateau, which yielding high energy density. However, the inferior interfacial stability between the bare NCA and sulfides limits its electrochemical performance. Hereien, the dual-electrolyte layer is proposed to mitigate this effect and enhance the battery performances of NCA-based ASSLIBs. The Li_(3)InCl_6 wih high conductivity and excellent electrochemcial stability act both as an ion additives to promote Li-ion diffusion across the interface in the cathode and as a buffer layer between the cathode layer and the solid electrolyte layer to avoid side reactions and improve the interface stability. The corresponding battery exhibits high discharge capacities and superior cyclabilities at both room and elevated temperatures. It exhibits discharge performance of 237.04 and216.07 m Ah/g at 0.1 and 0.5 C, respectively, when cycled at 60 ℃, and sustains 95.9% of the capacity after100 cycles at 0.5 C. The work demonstrates a simple strategy to ensure the superior performances of NCA in sulfide-based ASSLBs.展开更多
A series of solid solutions with high content of Tb_(2)O_(3)-(Tb_(x)Ti_(1−x))4O_(8−2x)(x=0.667-0.830)are synthesized in the Tb_(2)O_(3)-TiO_(2)system via co-precipitation and/or mechanical activation.This is followed ...A series of solid solutions with high content of Tb_(2)O_(3)-(Tb_(x)Ti_(1−x))4O_(8−2x)(x=0.667-0.830)are synthesized in the Tb_(2)O_(3)-TiO_(2)system via co-precipitation and/or mechanical activation.This is followed by high-temperature annealing for 4-22 h.The X-ray diffrac-tion method showed that the fluorite structure was realized for(Tb_(x)Ti_(1−x))4O_(8−2x)(x=0.75-0.817).The solid solution Tb_(3.12)Ti_(0.88)O_(6.44)(64mol%Tb_(2)O_(3)(x=0.78))with a fluorite structure exhibited a maximum hole conductivity of~22 S/cm at 600℃.To separate the ionic component of the conductivity in the electronic conductor Tb_(3.12)Ti_(0.88)O_(6.44),its high entropy analogue,(La_(0.2)Gd_(0.2)Tm_(0.2)Lu_(0.2)Y_(0.2))_(3.12)Ti_(0.88)O_(6.44),was synthesized in which all rare-earth elements(REE)cations exhibited valency of+3.Consequently,the contribution of ionic(proton)conductivity(~7×10^(−6)S/cm at 600℃)was revealed with respect to the background of dominant hole conductivity.The proton conduct-ivity of high-entropy oxide(HEО)(La_(0.2)Gd_(0.2)Tm_(0.2)Lu_(0.2)Y_(0.2))_(3.12)Ti_(0.88)O_(6.44)was confirmed by the detection of the isotope effect,where the mobility of the heavier O-D ions was lower than that of the O-H hydroxyls,resulting in lower conductivity in D_(2)O vapors when com-pared to H_(2)O.展开更多
The difficulty in fabricating a multifaceted composite heterojunction system based on Cd_(x) Zn_(1-x) S limits the enhancement of photocatalytic performance.In the present scrutiny,novel ZnO/Cd_(x) Zn_(1-x) S/CdS com-...The difficulty in fabricating a multifaceted composite heterojunction system based on Cd_(x) Zn_(1-x) S limits the enhancement of photocatalytic performance.In the present scrutiny,novel ZnO/Cd_(x) Zn_(1-x) S/CdS com-posite heterojunctions are successfully prepared by the alkaline dissolution etching method.The internal electric field at the interface of I-type and Z-scheme heterojunction improved the effective charge sepa-ration.The ZC 8 sample exhibits excellent photocatalytic performance and the H2 production efficiency is 15.67 mmol g^(−1) h^(−1) with good stability up to 82.9%in 24-hour cycles.The performance of CH_(4) and CO capacity in the CO_(2) RR process is 3.47μmol g^(−1) h^(−1) and 23.5μmol g^(−1) h^(−1),respectively.The photogener-ated accelerated charge transport is then examined in detail by in situ X-ray photoelectron spectroscopy(ISXPS)and density functional theory(DFT)calculations.This work presents a new idea for the synthe-sis of Cd_(x) Zn_(1-x) S solid-solution-based materials and provides a solid reference for the detailed mechanism regarding the electric field at the heterojunction interface.展开更多
CO_(2)reduction reaction(CO_(2)RR)electrolyzers based on gas diffusion electrode(GDE)enable the direct mass transfer of CO_(2)to the catalyst surface for participation in the reaction,thereby establishing an efficient...CO_(2)reduction reaction(CO_(2)RR)electrolyzers based on gas diffusion electrode(GDE)enable the direct mass transfer of CO_(2)to the catalyst surface for participation in the reaction,thereby establishing an efficient three-phase reaction interface that significantly enhances current density.However,current hydrophobic modification methods face difficulties in achieving precise and substantial control over wettability,and the hydrophobic modifiers tend to significantly impair the conductivity of the electrode and ion transport capabilities.This study employs Nafion ionomers to hydrophobically modify the threedimensional catalyst layer,revealing the bifunctionality of Nafion.The fluorinated backbone of Nafion ensures the hydrophobicity of the entire catalyst layer,while its sulfonic acid groups promote ion transport,without significantly affecting the conductivity of the electrode.Furthermore,by employing modifiers with distinct wettability characteristics,a highly efficient and large-scale manipulation of the hydrophilic/hydrophobic properties of the catalyst layer was successfully realized.The electrode,constructed with silver nanopowder as a representative catalyst and modified with the hydrophobic ionomer Nafion,exhibits a substantial enhancement in both catalytic activity and durability.The optimized electrode exhibited exceptional electrocatalytic performance in both flow cell and membrane electrode assembly(MEA)configurations.Notably,in the MEA,the electrode achieved a remarkable CO Faradaic efficiency(FE)of 93.3%at a total current density of 200 mA cm^(-2),while maintaining stable operation for over 62 h.展开更多
Background:Aspiration pneumonia is a severe health concern,particularly for ICU patients with impaired airway defenses.Current animal models fail to fully replicate the condition,focusing solely on chemical lung injur...Background:Aspiration pneumonia is a severe health concern,particularly for ICU patients with impaired airway defenses.Current animal models fail to fully replicate the condition,focusing solely on chemical lung injury from gastric acid while neglecting pathogen-induced inflammation.This gap hinders research on pathogenesis and treatment,creating an urgent need for a clinically relevant model.This study aimed to develop an improved rat model of aspiration pneumonia by combining hydrochloric acid(HCl)and lipopolysaccharide(LPS)administration.Methods:Specific pathogen-free Sprague Dawley rats underwent intratracheal instillation of HCl and LPS.Techniques included rat weight measurement,tracheal intubation,pulmonary function monitoring,lung tissue sampling with HE staining and scoring,bronchoalveolar lavage fluid(BALF)sampling,protein and inflammatory cytokine analysis via BCA and ELISA,BALF pH determination,Evans Blue dye assessment,blood gas analysis,FITC-dextran leakage,Western blotting,electron microscopy,survival analysis,and transcriptome sequencing with bioinformatics.Statistical analysis was performed using GraphPad Prism.Results:The optimal model involved instillation of 1.5μL/g.wt HCl(pH=1)followed by 20μg/g.wt LPS after 1 h.This model reproduced acute lung injury,including tissue damage,pulmonary microvascular dysfunction,inflammatory responses,hypoxemia,and impaired pulmonary ventilation,with recovery observed at 72 h.PANoptosis was confirmed,characterized by increased markers.Concentration-dependent effects of HCl and LPS on lung damage were identified,alongside cytokine elevation and microvascular dysfunction.Conclusions:This optimized model closely mimics clinical aspiration pneumonia,providing a valuable tool for studying pathophysiology and therapeutic strategies.展开更多
Dear Colleagues,It is my distinct honor to serve as the Honorary Chief Editor of AMEM,an international open-access journal,dedicated to serve as a platform for international exchange,and the translation of research ou...Dear Colleagues,It is my distinct honor to serve as the Honorary Chief Editor of AMEM,an international open-access journal,dedicated to serve as a platform for international exchange,and the translation of research outcomes in the field of life sciences.AMEM strives to establish itself as a high-level international academic exchange platform that brings together scientific wisdom from around the world and offers a prestigious journal for presenting research findings,and disseminating state of the art knowledge in the vibrant fields of life sciences.展开更多
Achieving high energy densities for all-solid-state lithium batteries is restricted by the poor high voltage stability of solid electrolytes.Herein,F-doping strategy is successfully employed on Li_(3)InCl_(6)to obtain...Achieving high energy densities for all-solid-state lithium batteries is restricted by the poor high voltage stability of solid electrolytes.Herein,F-doping strategy is successfully employed on Li_(3)InCl_(6)to obtain enhanced voltage stability and electrode compatability towards bare LiNi_(0.7)Mn_(0.2)Co_(0.1)O_(2)at high voltages.The optimized Li_(3)InCl_(5.5)F_(0.5)electrolyte exhibits a decreased conductivity of 1.00 m S/cm,a wider voltage window,and improved electrochemical performance in solid-state batteries when cycled at upper cut-off voltages of 4.5 and 4.8 V(vs.Li^(+)/Li^(0)).The generation of more stable LiInF4phase in the cathode mixture of Li3InCl5.5F0.5-based battery ensures superior electrochemical performances compared to the Li_(3)InCl_(6)-based battery.The former battery exhibits a higher discharge capacity of 218.9 m Ah/g and coulombic efficiency of 86.7%for the first cycle,and retains 80.0%of its original value after 100 cycles when cycled in the range of 3.0–4.5 V(vs.Li^(+)/Li^(0)).In contrast,the Li_(3)InCl_(6)-based battery exhibits lower capacities and faster degradation under the same conditions due to the formation of InCl^(3)phase with poor electrochemical stability.This work facilitates the advancement of high energy density solid-state battery technologies by utilizing high-voltage cathodes.展开更多
In direct ethylene glycol fuel cells,advanced anodic electrocatalysts are urgently required to achieve high energy efficiency and optimal fuel utilization for complete ethylene glycol electrooxidation.In this work,bim...In direct ethylene glycol fuel cells,advanced anodic electrocatalysts are urgently required to achieve high energy efficiency and optimal fuel utilization for complete ethylene glycol electrooxidation.In this work,bimetallic PtRh nanodendrites(PtRh NDs)with a three-dimensionally self-supporting structure,abundant(100)crystal facets,and numerous Pt/Rh active sites are synthesized using a simple wet chemical reduction method.The as-synthesized PtRh NDs exhibit outstanding electrocatalytic activity and remarkable selectivity for the ethylene glycol oxidation reaction(EGOR)in alkaline media,significantly enhancing the utilization of ethylene glycol fuel in fuel cells.Theoretical calculations demonstrate that the exposure of(100)crystal faces and the incorporation of Rh atoms play crucial roles in improving the activity and selectivity of EGOR.The present work not only provides an effective method for the synthesis of PtRh NDs with rich(100)crystal faces but also provides new insights into the synergistic effects between the crystal faces and the components in the electrocata lytic process.展开更多
REST(Rust-based electronic structure toolkit)is a modern open-source electronic structure code entirely written in Rust,combining high performance,memory safety,and expressive concurrency.As a community-driven project...REST(Rust-based electronic structure toolkit)is a modern open-source electronic structure code entirely written in Rust,combining high performance,memory safety,and expressive concurrency.As a community-driven project,its source code is freely available at https://gitee.com/restgroup,fostering open collaboration and transparent development.It supports a wide range of density functional methods-from local density approximation(LDA),generalized gradient approximation(GGA),meta-GGA,and hybrids to doubly hybrids,as well as machine learning-augmented functionals-enabling high-accuracy simulations with low computational overhead.Its“disk-free”RI-based(RI:resolution-of-the-identity)implementation and efficient shared-memory parallelism(via Rayon)ensure rapid calculations even for challenging systems.REST also of-fers unique user support through large language model-assisted input generation and develop-erfriendly tensor libraries for rapid algorithm prototyping.展开更多
The dehydrogenation of alkanes has emerged as a vital complementary process to address the increasing global demand for olefins.A key challenge remains in the construction of novel active centers that offer superior a...The dehydrogenation of alkanes has emerged as a vital complementary process to address the increasing global demand for olefins.A key challenge remains in the construction of novel active centers that offer superior activity,stability,and cost-effectiveness.Herein,tricoordinated cobalt atoms were successfully fabricated through an in-situ ligand-protected synthesis by introducing tungsten atoms into zeolite frameworks.These unsaturated Co species efficiently activate C-H bonds while suppressing C-C bond cleavage,resulting in exceptional catalytic activity and olefin selectivity in both propane and ethane dehydrogenation reactions.The optimized Co_(0.2%)@0.01W-S-1 catalyst demonstrated an impressive propylene formation rate of 15.2 molC_(3H6)gcC h^(-1)at 823 K and an ethylene formation rate of 240.3mol_(C2H4)g_(Co)^(-1)h^(-1)at 913 K,with propylene and ethylene selectivities of 99.0%and 97.5%,respectively.These results not only significantly surpass conventional tetracoordinated Co catalysts but also rival some Pt-based catalysts under similar conditions.Importantly,the catalyst exhibited excellent stability in dehydrogenation reactions,with no significant loss in catalytic activity after five consecutive regeneration cycles.This work offers valuable insights into the design of zeolite-supported non-precious metal catalysts with high activity and durability for efficient alkane dehydrogenation.展开更多
Calcium carbide,a bulky and cheap raw chemical,is traditionally depolymerized by water to release acetylene,allowing the downstream organic transformation.In this study,hydrogen sulfide(H_(2)S),an industrial waste gas...Calcium carbide,a bulky and cheap raw chemical,is traditionally depolymerized by water to release acetylene,allowing the downstream organic transformation.In this study,hydrogen sulfide(H_(2)S),an industrial waste gas,has been exploited to depolymerize calcium carbide,which represents a strategy for the comprehensive utilization of both hydrogen sulfide and calcium carbide.As a proof of concept,a three-component condensation reaction was established to prepare thioamides directly from hydrogen sulfide and calcium carbide in high yields.Leveraging the unique properties of thioamides that possess both nucleophilic sulfur and electrophilic carbon sites,a series of novel tandem reactions were further developed to construct structurally diverse heterocyclic compounds.Our strategy not only provides a new chemical pathway for calcium carbide depolymerization,but also offers a solution for the utilization of hazardous hydrogen sulfide gas.More importantly,this approach facilitates the comprehensive and sustainable utilization of the calcium carbide resource.展开更多
Thymoquinone(TQ)and gallic acid(GA)are known for counter-tumorigenic characteristics.GA inhibits cancer cell proliferation by interfering with many apoptotic signaling pathways,producing more reactive oxygen species(R...Thymoquinone(TQ)and gallic acid(GA)are known for counter-tumorigenic characteristics.GA inhibits cancer cell proliferation by interfering with many apoptotic signaling pathways,producing more reactive oxygen species(ROS),focusing on the cell cycle,and suppressing the expression of oncogenes and matrix metalloproteinases(MMPs).In this study,TQ(after reducing to thymohydroquinone)and GA are esterified to form thymohydroquinyl gallate(a prodrug).Thymohydroquinyl gallate(THQG)possesses enhanced antineoplastic efficacy and targeted delivery potential.The chemical and spectroscopic analysis confirms ester synthesis.Gold nanoparticles(AuNPs)are employed as nanocarriers due to their physicochemical and optical characteristics,biocompatibility,and low toxicity.As an efficient drug transporter,(AuNPs) shield conjugated drugs from enzymatic digestion.The prodrug acts as a reducing agent for Au metal atoms and is loaded onto it after reduction.The nano drug is radiolabeled with 99mTc and 131I to monitor the drug biodistribution in animals using a gamma camera and single-photon emission computerized tomography(SPECT).131I is an antineoplastic that helps enhance the drug's efficiency.Chromatographic results reveal promising radiolabeling percentages.In vitro,drug release shows sustained release at pH~5.8.In vitro 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide(MTT)cytotoxicity assay reveals drug potency on CAL 27 and MCF 7 cell lines.展开更多
Propane dehydrogenation(PDH)has emerged as a key on-purpose technology for the production of propylene,but it often depends on toxic chromium and expensive platinum catalysts,highlighting the need for environmentally ...Propane dehydrogenation(PDH)has emerged as a key on-purpose technology for the production of propylene,but it often depends on toxic chromium and expensive platinum catalysts,highlighting the need for environmentally friendly and cost-effective alternatives.In this study,we developed a facile impregnation method to fabricate unsaturated Co single-atoms with a tricoordinated Co_(1)O_(3)H_(x) structure by regulating silanol nests in purely siliceous Beta zeolites.Detailed PDH catalytic tests and characterizations revealed a positive correlation between the presence of silanol nests and enhanced catalytic activity.Additionally,the unsaturated Co single-atoms exhibited a carbon deposition rate more than an order of magnitude slower than that of Co nanoparticles.Notably,the optimized Co_(0.3%)/deAl-meso-Beta catalyst achieved a record-high propylene formation rate of 21.2 mmol_(C3H6) g_(cat)^(-1) h^(-1),with an exceptional propylene selectivity of 99.1%at 550℃.Moreover,the Co_(0.3%)/deAl-meso-Beta catalyst demonstrated excellent stability,with negligible deactivation after 5 consecutive regeneration cycles.This study emphasizes the pivotal role of silanol nests of zeolites in stabilizing and modulating the coordination environment of metallic active sites,providing valuable insights for the design of high-activity,high-stability,and low-cost PDH catalysts.展开更多
Pyrolysis has the potential of transforming waste into valuable products. Pyrolytic carbon black (PCB) is one of the most important products resulting from the pyrolysis of used tires. One of the most significant appl...Pyrolysis has the potential of transforming waste into valuable products. Pyrolytic carbon black (PCB) is one of the most important products resulting from the pyrolysis of used tires. One of the most significant applica-tions of modified pyrolytic carbon black is its use as pigment for offset printing ink to obtain high added values. Inverse gas chromatography (IGC) results show that a large quantity of inorganic matters and carbonaceous deposit are removed by treating the pyrolytic carbon black with nitric acid solution. Plenty of active sites originally occu-pied by inorganic ash and coke are recovered. The surface energy of pyrolytic carbon black (TWPC)modified by titanate-coupling agent-especially the specific interaction γ sspdetermined by the specific probe molecule, tolu-ene-shows the strong interaction between the TWPC and the synthetic resins. The offset printing ink performance confirms the IGC prediction. And TWPC has the great potential of applications in printing ink industry as pigment.展开更多
Pyrolysis has the potential of transforming waste into recyclable products. Pyrolytic carbon black (PCB) is one of the most important products from the pyrolysis of used tires. Techniques for surface modifications of ...Pyrolysis has the potential of transforming waste into recyclable products. Pyrolytic carbon black (PCB) is one of the most important products from the pyrolysis of used tires. Techniques for surface modifications of PCB have been developed. One of the most significant applications for modified PCB is to reinforce the rubber matrix to obtain high added values. The transverse relaxation and the chain dynamics of vulcanized rubber networks with PCB and modified PCB were studied and compared with those of the commercial carbon blacks using selective 1H transverse relaxation (T2) experiments and dipolar correlation effect (DCE) experiments on the stimulated echo. Demineralization and coupling agent modification not only intensified the interactions between the modified PCB and the neighboring polyisoprene chains, but also increased the chemical cross-link density of the vulcanized rubber with modified PCB. The mechanical testing of the rubbers with different kinds of carbon blacks showed that the maximum strain of the rubber with modified PCB was improved greatly. The mechanical testing results confirmed the conclusion obtained by nuclear magnetic resonance (NMR). PCB modified by the demineralization and NDZ-105 titanate coupling agent could be used to replace the commercial semi-reinforcing carbon black.展开更多
Multiple-metal catalysts （Ni-Mn-Ce-K/bauxite） for Water-Gas Shift （WGS） reaction were prepared by impregnation, and the catalytic structure and properties were investigated by N2 physical, XRD, H2-TPR, and CO-TPD....Multiple-metal catalysts （Ni-Mn-Ce-K/bauxite） for Water-Gas Shift （WGS） reaction were prepared by impregnation, and the catalytic structure and properties were investigated by N2 physical, XRD, H2-TPR, and CO-TPD. The results indicated that the addition of 7.5% CeO2 improved the activity of the WGS reaction obviously, and also increased the specific surface area and pore volume of the catalysts. The addition of CeO2 decreases the reduction temperature, enhanced the adsorption and activation of H2O2, and improved the adsorption content of CO. Besides, active sites were not changed and the number of active sites on catalysts did not increase obviously.展开更多
Electrochemical water treatment is an attractive technology for water desalination and softening due to its low energy consumption. Especially, capacitive Deionization(CDI) is promising as a future technology for wate...Electrochemical water treatment is an attractive technology for water desalination and softening due to its low energy consumption. Especially, capacitive Deionization(CDI) is promising as a future technology for water treatment. Graphene(rGO) has been intensively studied for CDI electrode because of its advantages such as excellent electrical conductivity and high specific surface area. However, its 2D dimensional structure with small specific capacitance, high resistance between layers and hydrophobicity degrades ion adsorption efficiency. In this work, we successfully prepared uniformly dispersed Fe3O4/rGO nanocomposite by simple thermal reactions and applied it as effective electrodes for CDI. Iron oxides play a role in uniting graphene sheets, and specific capacitance and wettability of electrodes are improved significantly;hence CDI performances are enhanced. The hardness removal of Fe3O4/rGO nanocomposite electrodes can reach 4.3 mg/g at applied voltage of 1.5V, which is 3 times higher than that of separate r GO electrodes.Thus this material is a promising candidate for water softening technology.展开更多
基金state assignments of Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry,Russian Academy of Sciences(No.124013000692-4 and 122112100037-4).
文摘Lithium iron phosphate(LFP)has found many applications in the field of electric vehicles and energy storage systems.However,the increasing volume of end-of-life LFP batteries poses an urgent challenge in terms of environmental sustainability and resource management.Therefore,the development and implementation of efficient LFP battery recycling methods are crucial to address these challenges.This article presents a novel,comprehensive evaluation framework for comparing different lithium iron phosphate relithiation techniques.The framework includes three main sets of criteria:direct production cost,electrochemical performance,and environmental impact.Each criterion is scored on a scale of 0–100,with higher scores indicating better performance.The direct production cost is rated based on material costs,energy consumption,key equipment costs,process duration and space requirements.Electrochemical performance is assessed by rate capability and cycle stability.Environmental impact is assessed based on CO_(2)emissions.The framework provides a standardized technique for researchers and industry professionals to objectively compare relithiation methods,facilitating the identification of the most promising approaches for further development and scale-up.The total average score across the three criterion groups for electrochemical,chemical,and hydrothermal relithiation methods was approximately 60 points,while sintering scored 39 points,making it the least attractive relithiation technique.Combining approaches outlined in publications with scores exceeding 60,a relithiation scheme was proposed to achieve optimal electrochemical performance with minimal resource consumption and environmental impact.The results demonstrate the framework’s applicability and highlight areas for future research and optimization in lithium iron phosphate cathode recycling.
基金the National Natural Science Foundation of China(Grant No.51776009)for the financial support.
文摘Effective utilization of hot electrons generated from the decay of surface plasmon resonance in metal nanoparticles is conductive to improve solar water splitting efficiency.Herein,Ag nanoparticles and reduced graphene oxide(rGO)co-decorated hierarchical TiO2 nanoring/nanotube arrays(TiO2 R/T)were facilely fabricated by using two-step electrochemical anodization,electrodeposition,and photoreduction methods.Comparative studies were conducted to elucidate the effects of rGO and Ag on the morphology,photoresponse,charge transfer,and photoelectric properties of TiO2.Firstly,scanning electron microscope images confirm that the Ag nanoparticles adhered on TiO2 R/T and TiO2 R/T-rGO have similar diameter of 20 nm except for TiO2 R-rGO/T.Then,the UV-Vis DRS and scatter spectra reveal that the optical property of the Ag-TiO2 R/T-rGO ternary composite is enhanced,ascribing to the visible light absorption of plasmonic Ag nanoparticles and the weakening effect of rGO on light scattering.Meanwhile,intensity-modulated photocurrent spectroscopy and photoluminescence spectra demonstrate that rGO can promote the hot electrons transfer from Ag nanoparticles to Ti substrate,reducing the photogenerated electron-hole recombination.Finally,Ag-TiO2 R/T-rGO photoanode exhibits high photocurrent density(0.98 mA cm?2)and photovoltage(0.90 V),and the stable H2 evolution rate of 413μL h?1 cm?2 within 1.5 h under AM 1.5 which exceeds by 1.30 times than that of pristine TiO2 R/T.In line with the above results,this work provides a reliable route synergizing rGO with plasmonic metal nanoparticles for photocatalysis,in which,rGO presents a broad absorption spectrum and effective photogenerated electrons transfer.
文摘Gluconic acid and its derivatives have been widely used in the food and pharmaceutical industries. Conventional processes that involve the conversion of glucose into gluconic acid via fermentation present several technological shortcomings as they involve energy-intensive wastewater treatment and complex enzyme separation. Greener oxidation processes over heterogeneous metal catalysts have attracted increasing attention worldwide. Au-, Pt-and Pd-based heterogeneous catalysts have been extensively used for the chemical oxidation of glucose to gluconic acid. Bimetallic catalysts synthesized by adding either noble or inexpensive metals have also presented excellent performance for the oxidations of glucose. In particular, particle size, which has been recognized as the most important factor that affect catalytic performances, could be rationally tuned by changing the types of support and ligand as well as the synthesis conditions. In this perspective review, we summarize and critically discuss the recent advances in the structural design of mono-and bimetallic catalysts for the oxidation of glucose in aqueous media. Furthermore, the challenges of developing catalysts for the green synthesis of gluconic acid have been highlighted. This review provides alternative insights for designing effective catalytic materials for the catalytic oxidation of bio-derived oxygenates over heterogeneous catalysts.
基金supported by the National Key Research and Development Program (No.2021YFB2500200)the National Natural Science Foundation of China (No.52177214)supported by China Fujian Energy Devices Science and Technology Innovation Laboratory Open Fund (No.21C-OP202211)。
文摘LiNi_(0.8)Co_(0.15)Al_(0.05)O_(2)(NCA) is a promising cathode for sulfide-based solid-state lithium batteries(ASSLBs)profiting from its high specific capacity and voltage plateau, which yielding high energy density. However, the inferior interfacial stability between the bare NCA and sulfides limits its electrochemical performance. Hereien, the dual-electrolyte layer is proposed to mitigate this effect and enhance the battery performances of NCA-based ASSLIBs. The Li_(3)InCl_6 wih high conductivity and excellent electrochemcial stability act both as an ion additives to promote Li-ion diffusion across the interface in the cathode and as a buffer layer between the cathode layer and the solid electrolyte layer to avoid side reactions and improve the interface stability. The corresponding battery exhibits high discharge capacities and superior cyclabilities at both room and elevated temperatures. It exhibits discharge performance of 237.04 and216.07 m Ah/g at 0.1 and 0.5 C, respectively, when cycled at 60 ℃, and sustains 95.9% of the capacity after100 cycles at 0.5 C. The work demonstrates a simple strategy to ensure the superior performances of NCA in sulfide-based ASSLBs.
基金the state assignment on the topic“Interdisciplinary approaches to the creation and study of micro-/nanostructured systems”(No.125012200595-8)Conductivity measurements of the samples were performed in accordance with the state task for FRC PCP and MC RAS(No.124013000692-4).
文摘A series of solid solutions with high content of Tb_(2)O_(3)-(Tb_(x)Ti_(1−x))4O_(8−2x)(x=0.667-0.830)are synthesized in the Tb_(2)O_(3)-TiO_(2)system via co-precipitation and/or mechanical activation.This is followed by high-temperature annealing for 4-22 h.The X-ray diffrac-tion method showed that the fluorite structure was realized for(Tb_(x)Ti_(1−x))4O_(8−2x)(x=0.75-0.817).The solid solution Tb_(3.12)Ti_(0.88)O_(6.44)(64mol%Tb_(2)O_(3)(x=0.78))with a fluorite structure exhibited a maximum hole conductivity of~22 S/cm at 600℃.To separate the ionic component of the conductivity in the electronic conductor Tb_(3.12)Ti_(0.88)O_(6.44),its high entropy analogue,(La_(0.2)Gd_(0.2)Tm_(0.2)Lu_(0.2)Y_(0.2))_(3.12)Ti_(0.88)O_(6.44),was synthesized in which all rare-earth elements(REE)cations exhibited valency of+3.Consequently,the contribution of ionic(proton)conductivity(~7×10^(−6)S/cm at 600℃)was revealed with respect to the background of dominant hole conductivity.The proton conduct-ivity of high-entropy oxide(HEО)(La_(0.2)Gd_(0.2)Tm_(0.2)Lu_(0.2)Y_(0.2))_(3.12)Ti_(0.88)O_(6.44)was confirmed by the detection of the isotope effect,where the mobility of the heavier O-D ions was lower than that of the O-H hydroxyls,resulting in lower conductivity in D_(2)O vapors when com-pared to H_(2)O.
基金financially supported by the National Key Re-search and Development Program of China[No.2022YFF1202500,2022YFF1202502]the National Natural Science Foundation of China[62071459]+1 种基金the Subject arrangement Foundation of Shen-zhen[No.JCYJ20180507182057026]the International Science and Technology Cooperation Project of Bingtuan[No.2022BC008]。
文摘The difficulty in fabricating a multifaceted composite heterojunction system based on Cd_(x) Zn_(1-x) S limits the enhancement of photocatalytic performance.In the present scrutiny,novel ZnO/Cd_(x) Zn_(1-x) S/CdS com-posite heterojunctions are successfully prepared by the alkaline dissolution etching method.The internal electric field at the interface of I-type and Z-scheme heterojunction improved the effective charge sepa-ration.The ZC 8 sample exhibits excellent photocatalytic performance and the H2 production efficiency is 15.67 mmol g^(−1) h^(−1) with good stability up to 82.9%in 24-hour cycles.The performance of CH_(4) and CO capacity in the CO_(2) RR process is 3.47μmol g^(−1) h^(−1) and 23.5μmol g^(−1) h^(−1),respectively.The photogener-ated accelerated charge transport is then examined in detail by in situ X-ray photoelectron spectroscopy(ISXPS)and density functional theory(DFT)calculations.This work presents a new idea for the synthe-sis of Cd_(x) Zn_(1-x) S solid-solution-based materials and provides a solid reference for the detailed mechanism regarding the electric field at the heterojunction interface.
基金National Key R&D Program of China(2023YFA1507902,2021YFA1500804)the National Natural Science Foundation of China(22121004,22038009,22250008)+2 种基金the Haihe Laboratory of Sustainable Chemical Transformations(CYZC202107)the Program of Introducing Talents of Discipline to Universities,China(No.BP0618007)the Xplorer Prize,China,for their financial support。
文摘CO_(2)reduction reaction(CO_(2)RR)electrolyzers based on gas diffusion electrode(GDE)enable the direct mass transfer of CO_(2)to the catalyst surface for participation in the reaction,thereby establishing an efficient three-phase reaction interface that significantly enhances current density.However,current hydrophobic modification methods face difficulties in achieving precise and substantial control over wettability,and the hydrophobic modifiers tend to significantly impair the conductivity of the electrode and ion transport capabilities.This study employs Nafion ionomers to hydrophobically modify the threedimensional catalyst layer,revealing the bifunctionality of Nafion.The fluorinated backbone of Nafion ensures the hydrophobicity of the entire catalyst layer,while its sulfonic acid groups promote ion transport,without significantly affecting the conductivity of the electrode.Furthermore,by employing modifiers with distinct wettability characteristics,a highly efficient and large-scale manipulation of the hydrophilic/hydrophobic properties of the catalyst layer was successfully realized.The electrode,constructed with silver nanopowder as a representative catalyst and modified with the hydrophobic ionomer Nafion,exhibits a substantial enhancement in both catalytic activity and durability.The optimized electrode exhibited exceptional electrocatalytic performance in both flow cell and membrane electrode assembly(MEA)configurations.Notably,in the MEA,the electrode achieved a remarkable CO Faradaic efficiency(FE)of 93.3%at a total current density of 200 mA cm^(-2),while maintaining stable operation for over 62 h.
基金supported by the National Natural Science Foundation of China(No.82272243)the Science and Technology Commission of Shanghai Municipality(No.22Y11900800).
文摘Background:Aspiration pneumonia is a severe health concern,particularly for ICU patients with impaired airway defenses.Current animal models fail to fully replicate the condition,focusing solely on chemical lung injury from gastric acid while neglecting pathogen-induced inflammation.This gap hinders research on pathogenesis and treatment,creating an urgent need for a clinically relevant model.This study aimed to develop an improved rat model of aspiration pneumonia by combining hydrochloric acid(HCl)and lipopolysaccharide(LPS)administration.Methods:Specific pathogen-free Sprague Dawley rats underwent intratracheal instillation of HCl and LPS.Techniques included rat weight measurement,tracheal intubation,pulmonary function monitoring,lung tissue sampling with HE staining and scoring,bronchoalveolar lavage fluid(BALF)sampling,protein and inflammatory cytokine analysis via BCA and ELISA,BALF pH determination,Evans Blue dye assessment,blood gas analysis,FITC-dextran leakage,Western blotting,electron microscopy,survival analysis,and transcriptome sequencing with bioinformatics.Statistical analysis was performed using GraphPad Prism.Results:The optimal model involved instillation of 1.5μL/g.wt HCl(pH=1)followed by 20μg/g.wt LPS after 1 h.This model reproduced acute lung injury,including tissue damage,pulmonary microvascular dysfunction,inflammatory responses,hypoxemia,and impaired pulmonary ventilation,with recovery observed at 72 h.PANoptosis was confirmed,characterized by increased markers.Concentration-dependent effects of HCl and LPS on lung damage were identified,alongside cytokine elevation and microvascular dysfunction.Conclusions:This optimized model closely mimics clinical aspiration pneumonia,providing a valuable tool for studying pathophysiology and therapeutic strategies.
文摘Dear Colleagues,It is my distinct honor to serve as the Honorary Chief Editor of AMEM,an international open-access journal,dedicated to serve as a platform for international exchange,and the translation of research outcomes in the field of life sciences.AMEM strives to establish itself as a high-level international academic exchange platform that brings together scientific wisdom from around the world and offers a prestigious journal for presenting research findings,and disseminating state of the art knowledge in the vibrant fields of life sciences.
基金supported by the National Key Research and Development Program of China(No.2021YFB2400300)the National Natural Science Foundation of China(Nos.52177214,22205153)for supporting。
文摘Achieving high energy densities for all-solid-state lithium batteries is restricted by the poor high voltage stability of solid electrolytes.Herein,F-doping strategy is successfully employed on Li_(3)InCl_(6)to obtain enhanced voltage stability and electrode compatability towards bare LiNi_(0.7)Mn_(0.2)Co_(0.1)O_(2)at high voltages.The optimized Li_(3)InCl_(5.5)F_(0.5)electrolyte exhibits a decreased conductivity of 1.00 m S/cm,a wider voltage window,and improved electrochemical performance in solid-state batteries when cycled at upper cut-off voltages of 4.5 and 4.8 V(vs.Li^(+)/Li^(0)).The generation of more stable LiInF4phase in the cathode mixture of Li3InCl5.5F0.5-based battery ensures superior electrochemical performances compared to the Li_(3)InCl_(6)-based battery.The former battery exhibits a higher discharge capacity of 218.9 m Ah/g and coulombic efficiency of 86.7%for the first cycle,and retains 80.0%of its original value after 100 cycles when cycled in the range of 3.0–4.5 V(vs.Li^(+)/Li^(0)).In contrast,the Li_(3)InCl_(6)-based battery exhibits lower capacities and faster degradation under the same conditions due to the formation of InCl^(3)phase with poor electrochemical stability.This work facilitates the advancement of high energy density solid-state battery technologies by utilizing high-voltage cathodes.
基金sponsored by the National Natural Science Foundation of China(22272103)the Programs of Science and Technology of Suzhou in China(ZXL2021448 and SYG202137)+4 种基金Science and Technology Innovation Team of Shaanxi Province(2022TD-35 and 2023-CX-TD-27)the Young Scientist Initiative Project of School of Materials Science and Engineering at Shaanxi Normal University(2024YSIP-MSE-SNNU004)the Fundamental Research Funds for the Central Universities(GK202505036)the Technology Innovation Leading Program of Shaanxi in ChinaSanqin Scholars Innovation Teams in Shaanxi Province in China。
文摘In direct ethylene glycol fuel cells,advanced anodic electrocatalysts are urgently required to achieve high energy efficiency and optimal fuel utilization for complete ethylene glycol electrooxidation.In this work,bimetallic PtRh nanodendrites(PtRh NDs)with a three-dimensionally self-supporting structure,abundant(100)crystal facets,and numerous Pt/Rh active sites are synthesized using a simple wet chemical reduction method.The as-synthesized PtRh NDs exhibit outstanding electrocatalytic activity and remarkable selectivity for the ethylene glycol oxidation reaction(EGOR)in alkaline media,significantly enhancing the utilization of ethylene glycol fuel in fuel cells.Theoretical calculations demonstrate that the exposure of(100)crystal faces and the incorporation of Rh atoms play crucial roles in improving the activity and selectivity of EGOR.The present work not only provides an effective method for the synthesis of PtRh NDs with rich(100)crystal faces but also provides new insights into the synergistic effects between the crystal faces and the components in the electrocata lytic process.
基金supported by the National Natural Science Foundation of China (Nos. 22125301, 22393911, 22393912, 22321003, 22233002)the Innovation Program for Quantum Science and Technology (2021ZD0303305)the robotic AI-Scientist platform of the Chinese Academy of Science。
文摘REST(Rust-based electronic structure toolkit)is a modern open-source electronic structure code entirely written in Rust,combining high performance,memory safety,and expressive concurrency.As a community-driven project,its source code is freely available at https://gitee.com/restgroup,fostering open collaboration and transparent development.It supports a wide range of density functional methods-from local density approximation(LDA),generalized gradient approximation(GGA),meta-GGA,and hybrids to doubly hybrids,as well as machine learning-augmented functionals-enabling high-accuracy simulations with low computational overhead.Its“disk-free”RI-based(RI:resolution-of-the-identity)implementation and efficient shared-memory parallelism(via Rayon)ensure rapid calculations even for challenging systems.REST also of-fers unique user support through large language model-assisted input generation and develop-erfriendly tensor libraries for rapid algorithm prototyping.
基金supported by the National Key R&D Program of China(Grant No.2022YFA1506000)Gusu Innovation and Entrepreneurship Leading Talents Program(ZXL2022497)+5 种基金Jiangsu Distinguished Professor programfinancial support by National Natural Science Foundation of China(Grant No.22301057)Natural Science Foundation of Hebei Province(Grant No.B2023201065)Science Research Project of Hebei Education Department(Grant No.BJK2024103)supported by the Open Research Fund of Shanghai Key Laboratory of High-resolution Electron MicroscopyOpen Project of State Key Laboratory of Supramolecular Structure and Materials(sklssm2024019),ShanghaiTech University。
文摘The dehydrogenation of alkanes has emerged as a vital complementary process to address the increasing global demand for olefins.A key challenge remains in the construction of novel active centers that offer superior activity,stability,and cost-effectiveness.Herein,tricoordinated cobalt atoms were successfully fabricated through an in-situ ligand-protected synthesis by introducing tungsten atoms into zeolite frameworks.These unsaturated Co species efficiently activate C-H bonds while suppressing C-C bond cleavage,resulting in exceptional catalytic activity and olefin selectivity in both propane and ethane dehydrogenation reactions.The optimized Co_(0.2%)@0.01W-S-1 catalyst demonstrated an impressive propylene formation rate of 15.2 molC_(3H6)gcC h^(-1)at 823 K and an ethylene formation rate of 240.3mol_(C2H4)g_(Co)^(-1)h^(-1)at 913 K,with propylene and ethylene selectivities of 99.0%and 97.5%,respectively.These results not only significantly surpass conventional tetracoordinated Co catalysts but also rival some Pt-based catalysts under similar conditions.Importantly,the catalyst exhibited excellent stability in dehydrogenation reactions,with no significant loss in catalytic activity after five consecutive regeneration cycles.This work offers valuable insights into the design of zeolite-supported non-precious metal catalysts with high activity and durability for efficient alkane dehydrogenation.
基金the National Natural Science Foundation of China(Nos.22379075,22471114,U23A20528)the Group Project of Developing Inner Mongolia through Talents from the Talents Work Leading Group under the CPC Inner Mongolia Autonomous Regional Committee(No.2025TEL04)+2 种基金Natural Science Foundation of Inner Mongolia Autonomous Region(No.2024LHMS02011)the Innovative Research Team in Universities of Inner Mongolia Autonomous Region(No.NMGIRT2212)Basic Scientific Research Funds of Universities directly under the Inner Mongolia Autonomous Region(Nos.ZTY2025013 and JY20240076)for financial support。
文摘Calcium carbide,a bulky and cheap raw chemical,is traditionally depolymerized by water to release acetylene,allowing the downstream organic transformation.In this study,hydrogen sulfide(H_(2)S),an industrial waste gas,has been exploited to depolymerize calcium carbide,which represents a strategy for the comprehensive utilization of both hydrogen sulfide and calcium carbide.As a proof of concept,a three-component condensation reaction was established to prepare thioamides directly from hydrogen sulfide and calcium carbide in high yields.Leveraging the unique properties of thioamides that possess both nucleophilic sulfur and electrophilic carbon sites,a series of novel tandem reactions were further developed to construct structurally diverse heterocyclic compounds.Our strategy not only provides a new chemical pathway for calcium carbide depolymerization,but also offers a solution for the utilization of hazardous hydrogen sulfide gas.More importantly,this approach facilitates the comprehensive and sustainable utilization of the calcium carbide resource.
文摘Thymoquinone(TQ)and gallic acid(GA)are known for counter-tumorigenic characteristics.GA inhibits cancer cell proliferation by interfering with many apoptotic signaling pathways,producing more reactive oxygen species(ROS),focusing on the cell cycle,and suppressing the expression of oncogenes and matrix metalloproteinases(MMPs).In this study,TQ(after reducing to thymohydroquinone)and GA are esterified to form thymohydroquinyl gallate(a prodrug).Thymohydroquinyl gallate(THQG)possesses enhanced antineoplastic efficacy and targeted delivery potential.The chemical and spectroscopic analysis confirms ester synthesis.Gold nanoparticles(AuNPs)are employed as nanocarriers due to their physicochemical and optical characteristics,biocompatibility,and low toxicity.As an efficient drug transporter,(AuNPs) shield conjugated drugs from enzymatic digestion.The prodrug acts as a reducing agent for Au metal atoms and is loaded onto it after reduction.The nano drug is radiolabeled with 99mTc and 131I to monitor the drug biodistribution in animals using a gamma camera and single-photon emission computerized tomography(SPECT).131I is an antineoplastic that helps enhance the drug's efficiency.Chromatographic results reveal promising radiolabeling percentages.In vitro,drug release shows sustained release at pH~5.8.In vitro 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide(MTT)cytotoxicity assay reveals drug potency on CAL 27 and MCF 7 cell lines.
文摘Propane dehydrogenation(PDH)has emerged as a key on-purpose technology for the production of propylene,but it often depends on toxic chromium and expensive platinum catalysts,highlighting the need for environmentally friendly and cost-effective alternatives.In this study,we developed a facile impregnation method to fabricate unsaturated Co single-atoms with a tricoordinated Co_(1)O_(3)H_(x) structure by regulating silanol nests in purely siliceous Beta zeolites.Detailed PDH catalytic tests and characterizations revealed a positive correlation between the presence of silanol nests and enhanced catalytic activity.Additionally,the unsaturated Co single-atoms exhibited a carbon deposition rate more than an order of magnitude slower than that of Co nanoparticles.Notably,the optimized Co_(0.3%)/deAl-meso-Beta catalyst achieved a record-high propylene formation rate of 21.2 mmol_(C3H6) g_(cat)^(-1) h^(-1),with an exceptional propylene selectivity of 99.1%at 550℃.Moreover,the Co_(0.3%)/deAl-meso-Beta catalyst demonstrated excellent stability,with negligible deactivation after 5 consecutive regeneration cycles.This study emphasizes the pivotal role of silanol nests of zeolites in stabilizing and modulating the coordination environment of metallic active sites,providing valuable insights for the design of high-activity,high-stability,and low-cost PDH catalysts.
基金Supported by the National Natural Science Foundation of China (No.20176051) and the Key Natural Science Foundation ofChina (No.20490205).
文摘Pyrolysis has the potential of transforming waste into valuable products. Pyrolytic carbon black (PCB) is one of the most important products resulting from the pyrolysis of used tires. One of the most significant applica-tions of modified pyrolytic carbon black is its use as pigment for offset printing ink to obtain high added values. Inverse gas chromatography (IGC) results show that a large quantity of inorganic matters and carbonaceous deposit are removed by treating the pyrolytic carbon black with nitric acid solution. Plenty of active sites originally occu-pied by inorganic ash and coke are recovered. The surface energy of pyrolytic carbon black (TWPC)modified by titanate-coupling agent-especially the specific interaction γ sspdetermined by the specific probe molecule, tolu-ene-shows the strong interaction between the TWPC and the synthetic resins. The offset printing ink performance confirms the IGC prediction. And TWPC has the great potential of applications in printing ink industry as pigment.
基金Project supported by the National Natural Science Foundation of China (Nos. 20490200 and 20176051), and the Project Based Per-sonnel Exchange Program with the China Scholarship Council and the German Academic Exchange Service
文摘Pyrolysis has the potential of transforming waste into recyclable products. Pyrolytic carbon black (PCB) is one of the most important products from the pyrolysis of used tires. Techniques for surface modifications of PCB have been developed. One of the most significant applications for modified PCB is to reinforce the rubber matrix to obtain high added values. The transverse relaxation and the chain dynamics of vulcanized rubber networks with PCB and modified PCB were studied and compared with those of the commercial carbon blacks using selective 1H transverse relaxation (T2) experiments and dipolar correlation effect (DCE) experiments on the stimulated echo. Demineralization and coupling agent modification not only intensified the interactions between the modified PCB and the neighboring polyisoprene chains, but also increased the chemical cross-link density of the vulcanized rubber with modified PCB. The mechanical testing of the rubbers with different kinds of carbon blacks showed that the maximum strain of the rubber with modified PCB was improved greatly. The mechanical testing results confirmed the conclusion obtained by nuclear magnetic resonance (NMR). PCB modified by the demineralization and NDZ-105 titanate coupling agent could be used to replace the commercial semi-reinforcing carbon black.
基金the Natural Science Foundation of Fujian Province of China (U0650011)the "Little Invention and Little Creation" of Fu-jian Province Innovation and Development Committee of China
文摘Multiple-metal catalysts （Ni-Mn-Ce-K/bauxite） for Water-Gas Shift （WGS） reaction were prepared by impregnation, and the catalytic structure and properties were investigated by N2 physical, XRD, H2-TPR, and CO-TPD. The results indicated that the addition of 7.5% CeO2 improved the activity of the WGS reaction obviously, and also increased the specific surface area and pore volume of the catalysts. The addition of CeO2 decreases the reduction temperature, enhanced the adsorption and activation of H2O2, and improved the adsorption content of CO. Besides, active sites were not changed and the number of active sites on catalysts did not increase obviously.
基金supported by international cooperation program for science and technology funded by the Ministry of Science,ICT&Future Planning(NRF-2014K1A3A1A09063208)
文摘Electrochemical water treatment is an attractive technology for water desalination and softening due to its low energy consumption. Especially, capacitive Deionization(CDI) is promising as a future technology for water treatment. Graphene(rGO) has been intensively studied for CDI electrode because of its advantages such as excellent electrical conductivity and high specific surface area. However, its 2D dimensional structure with small specific capacitance, high resistance between layers and hydrophobicity degrades ion adsorption efficiency. In this work, we successfully prepared uniformly dispersed Fe3O4/rGO nanocomposite by simple thermal reactions and applied it as effective electrodes for CDI. Iron oxides play a role in uniting graphene sheets, and specific capacitance and wettability of electrodes are improved significantly;hence CDI performances are enhanced. The hardness removal of Fe3O4/rGO nanocomposite electrodes can reach 4.3 mg/g at applied voltage of 1.5V, which is 3 times higher than that of separate r GO electrodes.Thus this material is a promising candidate for water softening technology.
