Improving creep strength of the fine-grained heat-affected zone of novel 9Cr martensitic heat-resistant steel via modified thermo-mechanical treatment

The infamous type Ⅳ failure within the fine-grained heat-affected zone (FGHAZ) in G115 steel weldments seriously threatens the safe operation of ultra-supercritical (USC) power plants.In this work,the traditional thermo-mechanical treatment was modified via the replacement of hot-rolling with cold rolling,i.e.,normalizing,cold rolling,and tempering (NCT),which was developed to improve the creep strength of the FGHAZ in G115 steel weldments.The NCT treatment effectively promoted the dissolution of preformed M_(23)C_(6)particles and relieved the boundary segregation of C and Cr during welding thermal cycling,which accelerated the dispersed reprecipitation of M_(23)C_(6) particles within the fresh reaustenitized grains during post-weld heat treatment.In addition,the precipitation of Cu-rich phases and MX particles was promoted evidently due to the deformation-induced dislocations.As a result,the interacting actions between precipitates,dislocations,and boundaries during creep were reinforced considerably.Following this strategy,the creep rupture life of the FGHAZ in G115 steel weldments can be prolonged by 18.6%,which can further push the application of G115 steel in USC power plants.

A Single-Layer Piezoelectric Composite Separator for Durable Operation of Li Metal Anode at High Rates

Piezoelectric ceramic and polymeric separators have been proposed to effectively regulate Li deposition and suppress dendrite growth,but such separators still fail to satisfactorily support durable operation of lithium metal batteries owing to the fragile ceramic layer or low-piezoelectricity polymer as employed.Herein,by combining PVDF-HFP and ferroelectric BaTiO_(3),we develop a homogeneous,single-layer composite separator with strong piezoelectric effects to inhibit dendrite growth while maintaining high mechanical strength.As squeezed by local protrusion,the polarized PVDF-HFP/BaTiO_(3)composite separator generates a local voltage to suppress the local-intensified electric field and further deconcentrate regional lithium-ion flux to retard lithium deposition on the protrusion,hence enabling a smoother and more compact lithium deposition morphology than the unpoled composite separator and the pure PVDF-HFP separator,especially at high rates.Remarkably,the homogeneous incorporation of BaTiO_(3)highly improves the piezoelectric performances of the separator with residual polarization of 0.086 pC cm^(-2)after polarization treatment,four times that of the pure PVDF-HFP separator,and simultaneously increases the transference number of lithium-ion from 0.45 to 0.57.Beneficial from the prominent piezoelectric mechanism,the polarized PVDF-HFP/BaTiO_(3)composite separator enables stable cyclic performances of Li||LiFePO_(4)cells for 400 cycles at 2 C(1 C=170 mA g^(-1))with a capacity retention above 99%,and for 600 cycles at 5 C with a capacity retention over 85%.

Mechanism of micro-wetting of highly hydrophobic coal dust in underground mining and new wetting agent development

The internal mechanism of the high hydrophobicity of the coal samples from the Pingdingshan mining area was studied through industrial,element,and surface functional group analysis.Laboratory testing and molecular dynamics simulations were employed to study the impact of three types of surfactants on the surface adsorption properties and wettability of highly hydrophobic bituminous coal.The results show that the surface of highly hydrophobic bituminous coal is compact,rich in inorganic minerals,and poorly wettable and that coal molecules are dominated by hydrophobic functional groups of aromatic rings and aliphatic structures.The wetting performance of surfactants as the intermediate carrier to connect coal and water molecules is largely determined by the interaction force between surfactants and coal(Fs-c)and the interaction force between surfactants and water(Fs-w),which effectively improve the wettability of modified coal dust via modifying its surface electrical properties and surface energy.A new type of wetting agent with a dust removal rate of 89%has been developed through discovery of a compound wetting agent solution with optimal wetting and settling performance.This paper provides theoretical and technical support for removing highly hydrophobic bituminous coal dust in underground mining.

Ni_(3)Fe/Ni_(4)S_(3)/Ni/C Mixed Crystal Composite Nanofibers Prepared by Electrospinning and Heat Treatment Methods for Oxygen Evolution Reaction

OER catalyst of Ni_(3)Fe/Ni_(4)S_(3)/Ni/C(NiFeSC series)mixed crystal composite nanofibers was prepared by electrospinning and atmospheric heat treatment process.The testing results indicate that the diameters of Ni_(3)Fe/Ni_(4)S_(3)/Ni/C composite nanofibers is about 200 nm,the grains size is about 1-3 nm,and the fiber surface is rough.The electrochemical test results show that the heterojunction of the prepared Ni_(3)Fe/Ni_(4)S_(3)/Ni/C hybrid crystal composite nanofiber has synergistic effect with sulfide,and exhibits good electrocatalytic activity of water decomposition and OER in alkaline system.The OER electrocatalytic performance of Ni_(3)Fe/Ni_(4)S_(3)/Ni/C composite electrode prepared via a heat treatment at 1000℃process was tested in 1 mol/L KOH electrolytes.The results show that the overpotential is about 298 mV,the Tafel slope is about 74 mV?dec-1,and the surface resistance is about 1.69Ω·cm^(2),at the current density of 10 mA·cm^(-2).

Dynamic Reliability Evaluation and Life Prediction of Transmission System of Multi-Performance Degraded Wind Turbine

Wind power is a kind of important green energy.Thus,wind turbines have been widely utilized around the world.Wind turbines are composed of many important components.Among these components,the failure rate of the transmission system is relatively high in wind turbines.It is because the components are subjected to aerodynamic loads for a long time.In addition,its inertial load will result in fatigue fracture,wear and other problems.In this situation,wind turbines have to be repaired at a higher cost.Moreover,the traditional reliability methods are difficult to deal with the above challenges when performing the reliability analysis of the transmission system of wind turbines.To solve this problem,a stress-strength interference model based on performance degradation is introduced.Based on considering the strength degradation of each component,the improved Monte Carlomethod simulation based on the Back Propagation neural network is used to obtain the curve of system reliability over time.Finally,the Miner linear cumulative damage theory and the Carten-Dolan cumulative damage theory method are used to calculate the cumulative damage and fatigue life of the gear transmission system.

Nickel Sulfide Modified NiCu Nanoalloy with Excellent Oxygen Evolution Reaction Properties Prepared through Electrospinning and Heat Treatment

Ni^(2+)/Cu^(2+)/SO_(4)^(2-)/polyvinyl alcohol precursor fibers with uniform diameters were prepared through electrospinning.Nickel-based composite nanoalloys containing Ni,Cu,and S were prepared through heat treatment in an Ar atmosphere.The experimental results show that the main components of the prepared nanoalloys are NiCu,Ni_(3)S_(2),Ni,and C.The nanoalloys exhibit fine grain sizes about 200-500 nm,which can increase with increasing heat treatment temperature.Electrochemical test results show that the nickel sulfidemodified NiCu nanoalloy composites exhibit excellent oxygen evolution reaction properties,and the oxygen evolution reaction properties gradually improve with the increasing heat treatment temperature.The sample prepared at 1 000℃ for 40 min show a low overpotential of 423 mV and a small Tafel slope of 134 mV·dec^(-1) at a current density of 10 mA·cm^(-2).

Self-Adaptive and Electric Field-Driven Protective Layer with Anchored Lithium Deposition Enable Stable Lithium Metal Anode

Lithium metal battery has great development potential because of its lowest electrochemical potential and highest theoretical capacity.However,the uneven deposition of Li^(+)flux in the process of deposition and stripping induces the vigorous growth of lithium dendrites,which results in severely battery performance degradation and serious safety hazards.Here,the tetragonal BaTiO3 polarized by high voltage corona was used to build an artificial protective layer with uniform positive polarization direction,which enables uniform Li^(+)flux.In contrast to traditional strategies of using protective layer,which can guide the uniform deposition of lithium metal.The ferroelectric protective layer can accurately anchor the Li^(+)and achieve bottom deposition of lithium due to the automatic adjustment of the electric field.Simultaneously,the huge volume changes caused by Li^(+)migration change of the lithium metal anode during charging and discharging is functioned to excite the piezoelectric effect of the protective layer,and achieve seamless dynamic tuning of lithium deposition/stripping.This dynamic effect can accurately anchor and capture Li^(+).Finally,the layer-modified Li anode enables reversible Li plating/stripping over 1500 h at 1 mA cm^(-2)and 50℃in symmetric cells.In addition,the assembled Li-S full cell exhibits over 300 cycles with N/P≈1.35.This work provides a new perspective on the uniform Li^(+)flux at the Li-anode interface of the artificial protective layer.

Performance optimization of chalcogenide catalytic materials in lithium-sulfur batteries:Structural and electronic engineering

Lithium-sulfur batteries(LSBs)boasting remarkable energy density have garnered significant attention within academic and industrial spheres.Nevertheless,the progression of LSBs remains constrained by the languid redox kinetics intrinsic to sulfur and the pronounced shuttle effect induced by lithium polysulfides(Li PSs),which seriously affecting the energy density,cycling life and rate capacity.The conceptualization and implementation of catalytic materials stand acknowledged as a propitious stratagem for orchestrating kinetic modulation,particularly in excavating the conversion of LiPSs and has evolved into a focal point for disposing.Among them,chalcogenide catalytic materials(CCMs)have shown satisfactory catalytic effects ascribe to the unique physicochemical properties,and have been extensively developed in recent years.Considering the lack of systematic summary regarding the development of CCMs and corresponding performance optimization strategies,herein,we initiate a comprehensive review regarding the recent progress of CCMs for effective collaborative immobilization and accelerated transformation kinetics of Li PSs.Following that,the modulation strategies to improve the catalytic activity of CCMs are summarized,including structural engineering(morphology engineering,surface/interface engineering,crystal engineering)and electronic engineering(doping and vacancy,etc.).Finally,the application prospect of CCMs in LSBs is clarified,and some enlightenment is provided for the reasonable design of CCMs serving practical LSBs.

Synchronous organic-inorganic co-intercalated ammonium vanadate cathode for advanced aqueous zinc-ion batteries

Vanadium-based cathode materials are attractive for aqueous zinc-ion batteries(AZIBs)owing to the high capacity from their open frameworks and multiple valences.However,the cycle stability and rate capability are still restricted by the low electrical conductivity and trapped diffusion kinetics.Here,we propose an organic-inorganic co-intercalation strategy to regulate the structure of ammonium vanadate(NH_(4)V_(4)O_(10),NVO).The introduction of Al^(3+)and polyaniline(PANI)induces the optimized layered structure and generation of urchin-like hierarchical construction(AP-NVO),based on heterogeneous nucleation and dissolution-recrystallization growth mechanism.Owing to these favorable features,the AP-NVO electrode delivers a desirable discharge capacity of 386 mA h g^(-1) at 1.0 A g^(-1),high-rate capability of 263 mA h g^(-1 )at 5.0 A g^(-1) and excellent cycling stability with 80.4%capacity retention over 2000 cycles at 5.0 A g^(-1).Such satisfactory electrochemical performance is believed to result from the enhanced reaction kinetics provided by the stable layered structure and a high intercalation pseudo-capacitance reaction.These results could provide enlightening insights into the design of layered vanadium oxide cathodematerials.

Achieving structurally stable O3-type layered oxide cathodes through site-specific cation-anion co-substitution for sodium-ion batteries

O3-type layered oxides have garnered great attention as cathode materials for sodium-ion batteries because of their abundant reserves and high theoretical capacity.However,challenges persist in the form of uncontrollable phase transitions and intricate Na^(+)diffusion pathways during cycling,resulting in compromised structural stability and reduced capacity over cycles.This study introduces a special approach employing site-specific Ca/F co-substitution within the layered structure of O_(3)-NaNi_(0.5)Mn_(0.5)O_(2) to effectively address these issues.Herein,the strategically site-specific doping of Ca into Na sites and F into O sites not only expands the Na^(+)diffusion pathways but also orchestrates a mild phase transition by suppressing the Na^(+)/vacancy ordering and providing strong metal-oxygen bonding strength,respectively.The as-synthesized Na_(0.95)Ca_(0.05)Ni_(0.5)Mn_(0.5)O_(1.95)F_(0.05)(NNMO-CaF)exhibits a mild O3→O3+O'3→P3 phase transition with minimized interlayer distance variation,leading to enhanced structural integrity and stability over extended cycles.As a result,NNMO-CaF delivers a high specific capacity of 119.5 mA h g^(-1)at a current density of 120 mA g^(-1)with a capacity retention of 87.1%after 100 cycles.This study presents a promising strategy to mitigate the challenges posed by multiple phase transitions and augment Na^(+)diffusion kinetics,thus paving the way for high-performance layered cathode materials in sodium-ion batteries.

Thermochemical decomposition of phosphogypsum with Fe-P slag via a solid-state reaction

Phosphogypsum is a solid waste sourced from the wet-process phosphoric acid industry,which causes severe environmental damages.Its utilization was limited by its high decomposition temperature and high energy consumption.Herein,an Fe-P slag,which is a solid waste that mainly comprises iron phosphide(FeP)and diiron phosphide(Fe_(2)P),can dramatically decrease the decomposition temperature of phosphogypsum.It was found that the Fe-P slag and CaSO_(4) can react as shown in the following reaction equation:2Fe_(1.5)P+3CaSO_(4)+6CO_(2)→Ca_(3)(PO_(4))_(2)+Fe_(3)O_(4)+3SO_(2)+6CO.Its reaction mechanism was further determined using the thermodynamic method.It was found that CaS was the key intermediate for this reaction.The CaSO_(4) conversion for this method can reach approximately 97%under the optimized roasting conditions:the molar ratio between Fe_(1.5) P and CaSO_(4) of 2:3,roasting temperature of 900℃,a roasting time of 8 h.

Microstructure refinement and second phase particle regulation of Mo-Y_(2)O_(3) alloys by minor TiC additive

The oxide dispersion strengthened Mo alloys(ODS-Mo)prepared by traditional ball milling and subsequent sintering technique generally possess comparatively coarse Mo grains and large oxide particles at Mo grain boundaries(GBs),which obviously suppress the corresponding strengthening effect of oxide addition.In this work,the Y_(2)O_(3) and TiC particles were simultaneously doped into Mo alloys using ball-milling and subsequent low temperature sintering.Accompanied by TiC addition,the Mo-Y_(2)O_(3) grains are sharply refined from 3.12 to 1.36μm.In particular,Y_(2)O_(3) and TiC can form smaller Y-Ti-O-C quaternary phase particles(~230 nm)at Mo GBs compared to single Y_(2)O_(3) particles(~420 nm),so as to these new formed Y-Ti-O-C particles can more effectively pin and hinder GBs movement.In addition to Y-Ti-O-C particles at GBs,Y_(2)O_(3),TiOx,and TiCx nanoparticles(<100 nm)also exist within Mo grains,which is significantly different from traditional ODS-Mo.The appearance of TiOx phase indicates that some active Ti within TiC can adsorb oxygen impurities of Mo matrix to form a new strengthening phase,thus strengthening and purifying Mo matrix.Furthermore,the pure Mo,Mo-Y_(2)O_(3),and Mo-Y_(2)O_(3)-TiC alloys have similar relative densities(97.4%-98.0%).More importantly,the Mo-Y_(2)O_(3)-TiC alloys exhibit higher hardness(HV0.2(425±25))compared to Mo-Y_(2)O_(3) alloys(HV0.2(370±25)).This work could provide a relevant strategy for the preparation of ultrafine Mo alloys by facile ball-milling.

Molybdenum Oxynitride Atomic Nanoclusters Bonded in Nanosheets of N-Doped Carbon Hierarchical Microspheres for Efficient Sodium Storage

Transition metal nitrides have attracted considerable attention as great potential anode materials due to their excellent metallic conductivity and high theoretical specific capacity.However,their cycling performance is impeded by their instability caused by the reaction mechanism.Herein,we report the engineering and synthesis of a novel hybrid architecture composed of MoO2.0N0.5 atomic nanoclusters bonded in nanosheets of N-doped carbon hierarchical hollow microspheres(MoO2.0N0.5/NC)as an anode material for sodium-ion batteries.The facile self-templating strategy for the synthesis of MoO2.0N0.5/NC involves chemical polymerization and subsequent one-step calcination treatments.The design is benefi-cial to improve the electrochemical kinetics,buffer the volume variation of electrodes during cycling,and provide more interfacial active sites for sodium uptake.Due to these unique structural and compositional merits,these MoO2.0N0.5/NC exhibits excellent sodium storage performance in terms of superior rate capability and stable long cycle life.The work shows a feasible and effective way to design novel host candidates and solve the long-term cycling stability issues for sodium-ion batteries.

Controlled Synthesis of Core-Shell Nickel Microspheres with Solid Core and Porous Shell by Precipitation and Thermal Decomposition Method

Nickel oxalate micro-spheres with core-shell structure of solid core and radiate shell were synthesized by precipitation method in a mixed water solution, with oxalic acid and nickel acetate as raw materials, through dropping ammonium hydroxide to adjust the solution pH value to about 8.0. Nickel microspheres with core-shell structure of solid core and porous shell were prepared by decomposing of nickel oxalate microspheres precursor at about 340 ℃ in argon atmosphere. The analyses of infrared spectroscopy(IR)indicates that the composition of the powders is nickel oxalate. The analyses of atomic absorption spectrometry(AAS) and organic elemental analysis(OEA) indicate that the molar ratio of(C2O4)^2-/Ni^2+ is about 1.02, close to the theoretical value of 1.0. The results of the thermo-gravimetric and differential thermal gravity analyses(TG-DTG) indicate that the molar ratio of(C2O4)^2-/Ni^2+ is about 1.06, also close to the theoretical value of 1.0.The analysis of X-ray diffraction(XRD) indicates that the composition of black powders as-prepared is nickel,which has a face-centered cubic crystal structure with average crystal grain size about 16.87 nm. The images of scanning electron microscopy(SEM) indicate that the morphology of nickel oxalate microspheres is a coreshell structure with solid core and radiate shell. The diameter of nickel oxalate microspheres is about 3 μm, and the shell consists of a large number of thin nanorods. The images of SEM also indicate that the morphology of nickel microspheres is a core-shell structure with solid core and porous shell. The diameter of nickel microspheres is about 2 μm, and the shell consists of a large number of nickel grains, surface holes and through holes. The diameter of nickel grains is about 50-100 nm, and the diameter of holes is about 50-200 nm.

Fabrication, characterization and electrochemical properties of porous palladium bulk samples with high porosity and hierarchical pore structure

In the present study,porous bulk palladium samples were prepared by sodium chloride salt powder spacer incorporation and removal combined with dealloying.The obtained porous Pd bulks were characterized by X‐ray diffraction,field‐emission scanning electron microscopy and N2adsorption isotherm measurements.The prepared porous Pd bulk samples showed a hierarchical pore structure,a high porosity of^88%,a high surface area of^54m2/g,and a compression strength of^0.5MPa.Electrochemical measurements were performed to evaluate the electrocatalytic properties of the porous Pd bulk samples,revealing their effectiveness for ethanol oxidation.

Development of digital organ-on-a-chip to assess hepatotoxicity and extracellular vesicle-based anti-liver cancer immunotherapy

Organ-on-a-chip systems have been increasingly recognized as attractive platforms to assess toxicity and to develop new therapeutic agents.However,current organ-on-a-chip platforms are limited by a“single pot”design,which inevitably requires holistic analysis and limits parallel processing.Here,we developed a digital organ-on-a-chip by combining a microwell array with cellular microspheres,which significantly increased the parallelism over traditional organ-on-a-chip for drug development.Up to 127 uniform liver cancer microspheres in this digital organ-on-a-chip format served as individual analytical units,allowing for analysis with high consistency and quick response.Our platform displayed evident anti-cancer efficacy at a concentration of 10μM for sorafenib,and had greater alignment than the“single pot”organ-on-a-chip with a previous in vivo study.In addition,this digital organ-on-a-chip demonstrated the treatment efficacy of natural killer cell-derived extracellular vesicles for liver cancer at 50μg/mL.The successful development of this digital organ-on-a-chip platform provides high-parallelism and a low-variability analytical tool for toxicity assessment and the exploration of new anticancer modalities,thereby accelerating the joint endeavor to combat cancer.

Fabrication and Characterization of TiAl Alloy by Fields Activated Sintering Technology(FAST)

Ti-47Al alloy was fabricated by multi-physical fields activated sintering technology(FAST).With the coupling effects of electrical and pressure fields as the dominant driving force,a nearly fulldensity(relative density:99.15%)TiAl alloy sample was obtained.The microstructural characterizations,phase transformation at different sintering temperatures and their contributions to mechanical properties were investigated.The results reveal that TiAl_(3)is the main phase when sintered at 600 and 700℃.When the sintering temperature reaches 800℃,the main phases are TiAl and Ti_(3)Al.With the increase of sintering temperature,the content of TiAl increases and that of Ti_(3)Al decreases.When the sintering temperature reaches 1000℃,the alloy with fine and uniform microstructure and good mechanical properties can be obtained.

Self-assemble Mechanism of Nickel Nanobelts Prepared by Sol-precipitation and Thermal Decomposition Route

Using the idea of material design and the design of reaction system and conditions,quasi-one-dimensional nano-materials with ribbon-like structure were successfully prepared.Nickel tartrate nanobelts were prepared by a sol-precipitation route,using nickel chloride hexahydrate and tartaric acid as raw materials,and using ammonium hydroxide as pH value modifier.Nickel nanobelts with smooth surface were prepared by a thermal-decomposition route at about 355℃for about 30 minutes,in CO_(2) atmosphere,using nickel tartrate nanobelts as precursor.The analyses of atomic absorption spectrometry(AAS),organic elemental analyzer(OEA),infrared spectroscopy(IR)and ultraviolet-visible spectroscopy(UV-Vis)indicate that the products as-prepared is nickel tartrate,which has octahedral configuration of co-ordination of nickel atoms.The images of scanning electron microscopy(SEM)indicate that the morphology of nickel tartrate as-prepared is an obvious belt structure with clear and smooth surface.The images of SEM also indicate that the nickel nanobelts have clear and smooth surface.The nickel nanobelts are about tens of micrometers in length,tens of nanometers in thickness,and 100-200 nanometers in width.

Experimental Study of Post-heated Steel Reinforced Recycled Concrete Columns Repaired with CFRP

The mechanical and thermal properties of steel reinforced concrete columns with CFRP reinforcement were examined after exposure to a high temperature of 500℃. The concrete made with normal and recycled coarse aggregate（RCA） was fabricated and three different RCA replacement ratios（0, 50%, and 100%） were investigated. The fatigue properties of steel reinforced concrete with RCA and CFRP reinforcement were tested for two million cycles at a frequency of 2.5 Hz. The test results show that the failure of strengthened specimens is mainly caused by rupture of CFRP jacket and buckling of inner section steel reinforcement. However, for the unstrengthened specimen, both of inner steel buckling and core concrete cracking are the main contributors to the damage. The load-bearing capacity, deformation and energy dissipation of the specimens during the fatigue test could be strengthened greatly by CFRP reinforcement. However, the CFRP reinforcement has little influence on the improvement of the stiffness of the specimens, which may be caused by a plastic damage accumulation during the early cycles of fatigue tests. Finally, a static test was conducted on the postfatigue specimens, the results showed that a large decrease in stiffness was observed for the specimens subjected to high temperature and fatigue, and the fatigue loading had a higher influence on the specimens than the high temperature.

荞麦芯衍生的富氮和富氧可控多孔碳用于高性能超级电容器

以荞麦芯为前驱体,通过一种简单有效的一步活化方法制备分层多孔碳。制备得到的多孔碳具有高比表面积(805.91 m^(2)/g)和高孔隙体积(0.60 cm^(3)/g)。在三电极体系下,以0.5 A/g电流密度充放电,多孔碳在6 mol/L KOH中提供了330 F/g的超高电容。特别是当电流密度增加到100 A/g时,其电容仍可达到140 F/g。此外,在双电极系统中,其多孔碳构建的对称电容器在6 mol/L KOH电解液中可提供6.1 W·h/kg的输出。因此,这项研究为超级电容器电极材料提供了一条简单低成本的制备方法。