Due to the limited hydration capacity,solidification/stabilization(S/S)with waste concrete powder(WCP)has a low strength.Carbonation can reduce carbon dioxide(CO_(2))emissions and improve strength of lead-contaminated...Due to the limited hydration capacity,solidification/stabilization(S/S)with waste concrete powder(WCP)has a low strength.Carbonation can reduce carbon dioxide(CO_(2))emissions and improve strength of lead-contaminated soil,but its mechanism and environmental behaviors are unclear.In light of this,a comprehensive study was conducted on the compressive strength,lead immobilization,conductivity characteristics,and carbonation mechanism of carbonated Pb-contaminated soils stabilized with WCP compared to calcining 600℃WCP.Results indicated that with carbonation,the compressive strength of the samples was significantly improved at the early stage(1 d),resulting in increased unconfined compressive strength(UCS)by 2.5-5.2 times due to the filling of pores by calcite.It negatively affected the lead immobilization capacity of highly doped(30%)samples,while this effect reversed after 3 d of carbonating due to the reduced alkaline environment.The lead immobilization capacity decreased after 28 d of carbonating due to the cracking of samples and the influence of a lower pH on the solubility of lead-carbonated hydroxide((PbCO_(3))_(2)Pb(OH)_(2)).The water evaporation(saturation<16.8%)led to dry shrinkage cracking and decreased UCS of the samples.Based on this finding,a conductivity model was developed for carbonated and cured samples,accurately predicting changes in saturation levels(R^(2)=0.98).A relationship between conductivity and UCS or lead immobilization capacity was proposed.This research proposed an innovative method for the reduction of CO_(2)emission as well as laid down a theoretical basis for the recovery of WCP and lead-contaminated soils through carbonation.展开更多
Amino acids are the building blocks of proteins and play vital roles in both biological systems and drug development.In recent years,increasing attention has been given to the functionalization of amino acid derivativ...Amino acids are the building blocks of proteins and play vital roles in both biological systems and drug development.In recent years,increasing attention has been given to the functionalization of amino acid derivatives.Since the introduction of therapeutic insulin in the early 20th century,the conjugation of drug molecules with amino acids and peptides has been pivotal in driving advancements in drug discovery and become an integral part of modern medical practice.Currently,over a hundred peptide-drug conjugates have received global approval and are widely used to treat diseases such as diabetes,cancer,chronic pain,and multiple sclerosis.Key technologies for conjugating peptides with bioactive molecules include antibody-drug conjugates(ADCs),peptide-drug conjugates(PDCs),and proteolysis targeting chimeras(PROTACs).Significant efforts have been dedicated to developing strategies for the modification of amino acids and peptides,with particular focus on site-selective C-H alkylation/arylation reactions.These reactions are crucial for synthesizing bioactive molecules,as they enable the precise introduction of functional groups at specific positions,thereby improving the pharmacological properties of the resulting compounds.展开更多
Reversible solid oxide cell(RSOC)is a new energy conversion device with significant applications,especially for power grid peaking shaving.However,the reversible conversion process of power generation/energy storage p...Reversible solid oxide cell(RSOC)is a new energy conversion device with significant applications,especially for power grid peaking shaving.However,the reversible conversion process of power generation/energy storage poses challenges for the performance and stability of air electrodes.In this work,a novel high-entropy perovskite oxide La_(0.2)Pr_(0.2)Gd_(0.2)Sm_(0.2)Sr_(0.2)Co_(0.8)Fe_(0.2)O_(3−δ)(HE-LSCF)is proposed and investigated as an air electrode in RSOC.The electrochemical behavior of HE-LSCF was studied as an air electrode in both fuel cell and electrolysis modes.The polarization impedance(Rp)of the HE-LSCF electrode is only 0.25Ω·cm^(2) at 800℃ in an air atmosphere.Notably,at an electrolytic voltage of 2 V and a temperature of 800℃,the current density reaches up to 1.68 A/cm^(2).The HE-LSCF air electrode exhibited excellent reversibility and stability,and its electrochemical performance remains stable after 100 h of reversible operation.With these advantages,HE-LSCF is shown to be an excellent air electrode for RSOC.展开更多
Both soil organic carbon (SOC) and iron (Fe) oxide content, among other factors, drive the formation and stability of soil aggregates.However, the mechanism of these drivers in greenhouse soil fertilized with organic ...Both soil organic carbon (SOC) and iron (Fe) oxide content, among other factors, drive the formation and stability of soil aggregates.However, the mechanism of these drivers in greenhouse soil fertilized with organic fertilizer is not well understood.In a 3-year field experiment, we aimed to investigate the factors which drive the stability of soil aggregates in greenhouse soil.To explore the impact of organic fertilizer on soil aggregates, we established four treatments:no fertilization (CK);inorganic fertilizer (CF);organic fertilizer (OF);and combined application of inorganic and organic fertilizers(COF).The application of organic fertilizer significantly enhanced the stability of aggregates, that is it enhanced the mean weight diameter, geometric mean diameter and aggregate content (%) of>0.25 mm aggregate fractions.OF and COF treatments increased the concentration of SOC, especially the aliphatic-C, aromatic-C and polysaccharide-C components of SOC, particularly in>0.25 mm aggregates.Organic fertilizer application significantly increased the content of free Fe(Fed), reactive Fe (Feo), and non-crystalline Fe in both bulk soil and aggregates.Furthermore, non-crystalline Fe showed a positive correlation with SOC content in both bulk soil and aggregates.Both non-crystalline Fe and SOC were significantly positively correlated with>2 mm mean weight diameter.Overall, we believe that the increase of SOC, aromatic-C, and non-crystal ine Fe concentrations in soil after the application of organic fertilizer is the reason for improving soil aggregate stability.展开更多
Approximately 3.44 billion tons of copper mine tailings(MT)were produced globally in 2018 with an increase of 45%from 2010.Significant efforts are being made to manage these tailings through storage facilities,recycli...Approximately 3.44 billion tons of copper mine tailings(MT)were produced globally in 2018 with an increase of 45%from 2010.Significant efforts are being made to manage these tailings through storage facilities,recycling,and reuse in different industries.Currently,a large portion of tailings are managed through the tailing storage facilities(TSF)where these tailings undergo hydro-thermal-mechanical stresses with seasonal cycles which are not comprehensively understood.This study presents an investigative study to evaluate the performance of control and cement-stabilized copper MT under the influence of seasonal cycles,freeze-thaw(F-T)and wet-dry(W-D)conditions,representing the seasonal variability in the cold and arid regions.The control and cement-stabilized MT samples were subjected to a maximum of 12 F-T and 12 W-D cycles and corresponding micro-and-macro behavior was investigated through scanning electron microscope(SEM),volumetric strain(εvT,wet density(r),moisture content loss,and unconfined compressive strength(UCS)tests.The results indicated the vulnerability of Copper MT to 67%and 75%strength loss reaching residual states with 12 F-T and 8 W-D cycles,respectively.Whereas the stabilized MT retained 39%-55%and 16%-34%strength with F-T and W-D cycles,demonstrating increased durability.This research highlights the impact of seasonal cycles and corresponding strength-deformation characteristics of control and stabilized Copper MT in cold and arid regions.展开更多
oil aggregates profoundly impact soil sustainability and crop productivity, and they are influenced by complexinteractions between minerals and organics. This study aimed to elucidate the alterations in mineralogy and...oil aggregates profoundly impact soil sustainability and crop productivity, and they are influenced by complexinteractions between minerals and organics. This study aimed to elucidate the alterations in mineralogy and soilorganic carbon(SOC) following long-term green manure incorporation and the effect on soil aggregates. Based on 5-and 36-year field experiments, surface soil samples(0–20 cm) were collected from Alfisol and Ferrisol soilssubjected to rice–rice–winter fallow(CK) and rice–rice–Chinese milk vetch(MV) treatments to investigate aggregatestability, mineralogy, SOC composition, and soil microstructural characteristics. The results showed that high clay-content Ferrisol exhibited greater aggregate stability than low clay-content Alfisol. The phyllosilicates in Alfisolprimarily comprised illite and vermiculite, whereas those in Ferrisol with high-content free-form Fe oxides(Fed) weredominated by kaolinite. Additionally, the clay fraction in Ferrisol contained more aromatic-C than the clay fraction inAlfisol. The 36-year MV incorporation significantly increased the Ferrisol macroaggregate stability(9.57–13.37%),and it also facilitated the transformation of vermiculite into kaolinite and significantly increased the clay, Fed, and aromatic-C contents in Ferrisol. Backscattered electron(BSE)-scanning electron microscopy/energy dispersive X-ray spectroscopy(SEM/EDS) revealed a compact aggregate structure in Ferrisol with co-localization of Feoxides and kaolinite. Moreover, the partial least path model(PLS-PM) revealed that clay content directly improvedmacroaggregate stability, and that kaolinite and Fed positively and directly affected clay or indirectly modulated clay formation by increasing the aromatic-C levels. Overall, long-term MV incorporation promotes clay aggregation by affecting mineral transformation to produce more kaolinite and Fe oxides and retain aromatic-C, and it ultimately improves aggregate stability.展开更多
Wellbore instability is one of the significant challenges in the drilling engineering and during the development of carbonate reservoirs,especially with open-hole completion.The problems of wellbore instability such a...Wellbore instability is one of the significant challenges in the drilling engineering and during the development of carbonate reservoirs,especially with open-hole completion.The problems of wellbore instability such as downhole collapse and silt deposit in the fractured carbonate reservoir of Tarim Basin(Ordovician)are severe.Solid destabilization and production(SDP)was proposed to describe this engineering problem of carbonate reservoirs.To clarify the mechanism and mitigate potential borehole instability problems,we conducted particle size distribution(PSD)analysis,X-ray diffraction(XRD)analysis,triaxial compression tests,and micro-scale sand production tests based on data analysis.We found that the rock fragments and silt in the wellbore came from two sources:one from the wellbore collapse in the upper unplugged layers and the other from the production of sand particles carried by the fluid in the productive layers.Based on the experimental study,a novel method combining a geomechanical model and microscopic sand production model was proposed to predict wellbore instability and analyze its influencing factors.The critical condition and failure zone predicted by the prediction model fit well with the field observations.According to the prediction results,the management and prevention measures of wellbore instability in carbonate reservoirs were proposed.It is suggested to optimize the well track in new drilling wells while upgrading the production system in old wells.This study is of great guiding significance for the optimization of carbonate solid control and it improves the understanding of the sand production problems in carbonate reservoirs.展开更多
Photothermal catalytic methane dry reforming(DRM)technology can convert greenhouse gases(i.e.CH_(4)and CO_(2))into syngas(i.e.H_(2)and CO),providing more opportunities for reducing the greenhouse effect and achieving ...Photothermal catalytic methane dry reforming(DRM)technology can convert greenhouse gases(i.e.CH_(4)and CO_(2))into syngas(i.e.H_(2)and CO),providing more opportunities for reducing the greenhouse effect and achieving carbon neutrality.In the DRM field,Ni-based catalysts attract wide attention due to their low cost and high activity.However,the carbon deposition over Ni-based catalysts always leads to rapid deactivation,which is still a main challenge.To improve the long-term stability of Ni-based catalysts,this work proposes a carbon-atom-diffusion strategy under photothermal conditions and investigates its effect on a Zn-doped Ni-based photothermal catalyst(Ni_(3)Zn@CeO_(2)).The photothermal catalytic behavior of Ni_(3)Zn@CeO_(2)can maintain more than 70 h in DRM reaction.And the photocatalytic DRM activity of Ni_(3)Zn@CeO_(2)is 1.2 times higher than thermal catalytic activity.Density functional theory(DFT)calculation and experimental characterizations indicate that Ni_(3)Zn promotes the diffusion of carbon atoms into the Ni_(3)Zn to form the Ni_(3)ZnC0.7 phase with body-centered cubic(bcc)structure,thus inhibiting carbon deposition.Further,in-situ diffuse reflectance infrared Fourier transform(DRIFT)spectroscopy and DFT calculation prove Ni_(3)Zn@CeO_(2)benefits the CH_(4)activation and inhibits the carbon deposition during the DRM process.Through inducing carbon atoms diffusion within the Ni_(3)Zn lattice,this work provides a straightforward and feasible strategy for achieving efficient photothermal catalytic DRM and even other CH_(4)conversion implementations with long-term stability.展开更多
Extending the charging voltage of LiCoO_(2)(LCO)is an ongoing and promising approach to increase its energy density.However,the main challenge of the approach lies in the insuperable cathodic interfacial processes at ...Extending the charging voltage of LiCoO_(2)(LCO)is an ongoing and promising approach to increase its energy density.However,the main challenge of the approach lies in the insuperable cathodic interfacial processes at high voltage,which leads to rapid failure both in the performance and structure of the LCO cathode.Herein,a Li_(2)CO_(3)-based additive was prepared by a simple sand-milling method,enabling a low electrochemical decomposition voltage<4.6 V from commonly>4.8 V,stabilizing the interface of the LCO cathode at 4.6 V.The decomposition of Li_(2)CO_(3)provides extra Li^(+)and CO_(2)to supplement the Li consumption required in the initial irreversible interfacial reactions and rapidly form a uniform and stable cathode electrolyte interphase layer(less organic and more inorganic components)on the LCO cathode by reducing CO_(2).Thus,the phase transformation and the emergence of high-valent Co ions on the surface of LCO at 4.6 V high voltage were inhibited.Thanks to this,with 2%Li_(2)CO_(3)-based additive,the capacity retention of commercial LCO at a high voltage of 4.6 V at 0.5 C for 100 cycles was improved from 59.3%to 79.3%.This work improves the high-voltage stability of LCO and provides a new idea for realizing the high-voltage operation of batteries.展开更多
In view of the volume instability of steel slag aggregate leading to the quality problem of expansion damage in asphalt road construction,the 4.75-9.5 mm steel slag particles were treated by autoclaved carbonation tec...In view of the volume instability of steel slag aggregate leading to the quality problem of expansion damage in asphalt road construction,the 4.75-9.5 mm steel slag particles were treated by autoclaved carbonation technology,and the effects of the carbonation system(temperature and time)on the autoclaved pulverization rate,f-CaO content,and the relationship between them for the carbonated steel slag were investigated.In addition,the microstructure of the carbonated steel slag was analyzed by X-ray diffractometer(XRD),scanning electron microscope and energy dispersive spectrometer(SEM-EDS),metallographic microscope and X-ray fluorescence imaging spectrometer(XRF).The experimental results indicate that,under the initial CO_(2)pressure of 1.0 MPa,increasing the carbonation temperature leads to the increase in the crystal plane spacing of Ca(OH)_(2)that was generated by the hydration of minerals in steel slag,and promotes the transformation of carbonated CaCO_(3)from the orthorhombic system to the hexagonal system,resulting in the increase of the crystal planes spacing of them,meantime,accelerates the decomposition of RO phases and also the outward migration of Ca^(2+),Fe^(2+),and Mn^(2+)ions to cover and coat on the Si^(4+),Al^(3+)ions,and impels the formation of hydroxides such as Fe(OH)_(3)and the formation of carbonates such as Ca(Mg)CO_(3),FeCO_(3)and MnCO_(3).Carbonation at the temperature of 90℃for 3 h can reach the center of 4.75-9.5 mm steel slag particles.Meanwhile,the increase of temperature can promote the mineral reaction in steel slag,resulting in the fuzzy interface between mineral phases,increase of burrs,dispersion,crossover,reduction of grain size,and rearrangement of mineral particles.展开更多
Global climate change exerts profound effects on snow cover,with consequential impacts on microbial activities and the stability of soil organic carbon(SOC)within aggregates.Northern peatlands are significant carbon r...Global climate change exerts profound effects on snow cover,with consequential impacts on microbial activities and the stability of soil organic carbon(SOC)within aggregates.Northern peatlands are significant carbon reservoirs,playing a critical role in mitigating climate change.However,the effects of snow variations on microbial-mediated SOC stability within aggregates in peatlands remain inadequately understood.Here,an in-situ field experiment manipulating snow conditions(i.e.,snow removal and snow cover)was conducted to investigate how snow variations affect soil microbial community and the associated SOC stability within soil aggregates(>2,0.25-2,and<0.25 mm)in a peatland of Northeast China.The results showed that snow removal significantly increased the SOC content and stability within aggregates.Compared to the soils with snow cover,snow removal resulted in decreased soil average temperatures in the topsoil(0-30 cm depth)and subsoil(30-60 cm depth)(by 1.48 and 1.34°C,respectively)and increased freeze-thaw cycles(by 11 cycles),consequently decreasing the stability of aggregates in the topsoil and subsoil(by 23.68%and 6.85%,respectively).Furthermore,more recalcitrant carbon and enhanced SOC stability were present in microaggregates(<0.25 mm)at two soil depths.Moreover,reductions in bacterial diversity and network stability were observed in response to snow removal.Structural equation modeling analysis demonstrated that snow removal indirectly promoted(P<0.01)SOC stability by regulating carbon to nitrogen(C:N)ratio within aggregates.Overall,our study suggested that microaggregate protection and an appropriate C:N ratio enhanced carbon sequestration in response to climate change.展开更多
Constructing silicon(Si)-based composite electrodes that possess high energy density,long cycle life,and fast charging capability simultaneously is critical for the development of high performance lithium-ion batterie...Constructing silicon(Si)-based composite electrodes that possess high energy density,long cycle life,and fast charging capability simultaneously is critical for the development of high performance lithium-ion batteries for mitigating range anxiety and slow charging issues in new energy vehicles.Herein,a thick silicon/carbon composite electrode with vertically aligned channels in the thickness direction(VC-SC)is constructed by employing a bubble formation method.Both experimental characterizations and theoretical simulations confirm that the obtained vertical channel structure can effectively address the problem of sluggish ion transport caused by high tortuosity in conventional thick electrodes,conspicuously enhance reaction kinetics,reduce polarization and side reactions,mitigate stress,increase the utilization of active materials,and promote cycling stability of the thick electrode.Consequently,when paired with LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)(NCM622),the VC-SC||NCM622 pouch type full cell(~6.0 mAh cm^(-2))exhibits significantly improved rate performance and capacity retention compared with the SC||NCM622 full cell with the conventional silicon/carbon composite electrode without channels(SC)as the anode.The assembled VC-SC||NCM622 pouch full cell with a high energy density of 490.3 Wh kg^(-1)also reveals a remarkable fast charging capability at a high current density of 2.0 mA cm^(-2),with a capacity retention of 72.0%after 500 cycles.展开更多
Evaluating the stabilized lead(Pb)-contaminated soils through sampling and laboratory testing involves costly and time-consuming processes.Therefore,this study employed a low-cost and non-destructive resistivity tool ...Evaluating the stabilized lead(Pb)-contaminated soils through sampling and laboratory testing involves costly and time-consuming processes.Therefore,this study employed a low-cost and non-destructive resistivity tool to evaluate the Pb-contaminated soils stabilized by electrolytic manganese residue(EMR)-based geopolymer(EG-OPC)from the strength and environmental benefits perspective.First,unconfined compressive strength(UCS)and leaching tests were conducted to study the stabilization effectiveness of EG-OPC.Results indicated that the UCS values of soil(5000 mg/kg of pollutants)stabilized by 20%EG-OPC were 4.87 MPa and 8.13 MPa after 7 d and 60 d of curing,respectively.After 60 d of curing,the Pb concentration in the leachate reached 44 mg/L,far lower than the control group(321 mg/L).Second,soil,pore water,and leachate resistivity(ERS,ERW,and ERL)were measured to establish fitting relationships with strength parameters and pollution risk.The good fitting results(e.g.ERS/ERW versus UCS/secant modulus(E50):correlation coefficient R2 z 0.9,ERS/ERW versus Pb contents:R2 z 0.9,and ERL versus Pb2þconcentration:R2¼0.92)and well used Archie's law(ERS versus ERW:R2>0.9)indicate that the resistivity can be used to evaluate the stabilization effectiveness.Furthermore,the microscopic results revealed two behaviors,demonstrating the reliability of resistivity:(1)with the hydration process,resistivity increases due to a denser structure and lower amounts of free water and Pb ions,and(2)the addition of Pb reduces resistivity due to its inhibition or even destructive effects on cementation and formation of hydration products.展开更多
Carbon fibres have been produced from hydroxypropyl-modified lignin(TcC)/bio-based polyamide 1010(PA1010)blended filaments.Two grades of PA1010,with different molecular weights and rheological properties,were used for...Carbon fibres have been produced from hydroxypropyl-modified lignin(TcC)/bio-based polyamide 1010(PA1010)blended filaments.Two grades of PA1010,with different molecular weights and rheological properties,were used for blending with TcC.An oxidative thermal stabilisation step was used prior to carbonisation in an inert atmosphere to prevent the fusion of the filaments during the latter step.Thermal stabilisation was not possible using a one-step stabilisation process reported in the literature for lignin and other lignin/synthetic polymer blends.As a consequence,a cyclic process involving an additional isothermal phase at a lower temperature than the precursor filaments’melting point,was introduced to increase the cross-linking reactions between the lignin and polyamide.Thermally stabilised filaments were characterised by DSC,TGA,TGA-FTIR,ATR,and SEM techniques.Polymer rheology and heating rate used during thermal stabilisation influenced the thermal stabilisation process and mechanical properties of the derived filaments.Thermally stabilised filaments using optimised conditions(heating in the air atmosphere at 0.25℃/min to 180℃;isothermal for 1 h,cooling back down to ambient at 5℃/min;heating to 250℃ at 0.25℃/min,isothermal for 2 h)could be successfully carbonised.Carbon fibres pro-duced had void-free morphologies and mechanical properties comparable to similarly thermally stabilised and carbonised polyacrylonitrile(PAN)filaments.展开更多
It is economical to perform methane and carbon dioxide reforming(DRM)under industrially relevant high-pressure conditions,but the harsh operation condition poses a grand challenge for coke-resistant catalyst design.He...It is economical to perform methane and carbon dioxide reforming(DRM)under industrially relevant high-pressure conditions,but the harsh operation condition poses a grand challenge for coke-resistant catalyst design.Here,we propose to boost the coke-tolerance of Co catalyst by applying a contact potential introduced by immiscible Ag clusters.We demonstrate that Co clusters separated by neighboring Ag on Yttria-stabilized zirconia(YSZ)support can serve as a coke-and sintering-resistant DRM catalyst under diluent gas-free,stoichiometric CH_(4) and CO_(2) feeding,1123 K and 20 bar.Since immiscible metals are ubiquitous and metal contact influences surface work function in general,this new design concept may have general implications for tailoring catalytic properties of metals.展开更多
Rich-nickel layered ternary NCM811 has been widely used in the field of electric vehicles ascribed to its high theoretical specific capacity.However,poor cycling stability and rate-performance hindered its further dev...Rich-nickel layered ternary NCM811 has been widely used in the field of electric vehicles ascribed to its high theoretical specific capacity.However,poor cycling stability and rate-performance hindered its further development.Herein,different amounts of nitrogen-doped carbon were wrapped on the surface of NCM811 via a facile rheological phase method by regulating the amount of dopamine hydrochloride.The effects of the coating amounts on the structure and electrochemical performance are investigated.The DFT calculation,XRD,SEM and XPS reveal that an appropriate amount of nitrogen-doped carbon coating could uniformly form a protective layer on the NCM811 surface and the introduced N could anchor Ni atoms to inhibit the Li^(+)/Ni^(2+)mixing,but excessive amount would reduce Ni^(3+)to Ni^(2+)so as to conversely aggravate Li^(+)/Ni^(2+)mixing.Among the samples,the NCM811-CN0.75 sample exhibits the most excellent electrochemical performance,delivering a high-rate capacity of 151.6 mA·h/g at 10C,and long-term cyclability with 82.2%capacity retention after 300 cycles at 5C,exhibiting remarkable rate-performance and cyclability.展开更多
A slurry-phase carbonation technique was utilized,employing argon oxygen decarburization slag(AOD slag)as a source of calcium and MgCl_(2) as a regulator for the crystal morphology of acicular aragonite.Subsequently,t...A slurry-phase carbonation technique was utilized,employing argon oxygen decarburization slag(AOD slag)as a source of calcium and MgCl_(2) as a regulator for the crystal morphology of acicular aragonite.Subsequently,the carbonated AOD slag,enriched with acicular aragonite,was employed in fabricating composite cementitious materials,followed by an analysis of their evolution in hydration heat,hydration products,and microscopic morphology.Additionally,it delved into the mechanism through which acicular aragonite enhances the stength of composite cementitious materials.Moreover,advanced simulation software for engineering and sciences(ABAQUS)was utilized to simulate the compressive performance of composite mortar with varying dosages of acicular aragonite.The findings demonstrate that the carbonated AOD slag,containing 83.4%acicular aragonite(with an average aspect ratio of 21.31),exhibited commendable compatibility with cement.Moderate integration of carbonated AOD slag facilitated the formation of calcium sulfoaluminate hydrate(AFt)phases.The acicular aragonite within the cementitious matrix showcased remarkable filling effects.As the dosage of carbonated AOD slag increased,flexural and compressive strengths of cement mortar initially rose before declining.Upon reaching a 6%cement inclusion of carbonated AOD slag,the various constituents of the cementitious material displayed optimal synergy.The numerical simulation results confirmed the experimental findings,demonstrating a favorable increase in compressive strength and flexural strength with the addition of acicular aragonite.The acicular aragonite strengthened the matrix by serving bridging and pull-out functions.展开更多
The traditional cement-based stabilization cannot effectively stabilize the marine soft clay under submerged conditions.In order to solve this problem,the enhancement of cement-stabilized marine soft clay was investig...The traditional cement-based stabilization cannot effectively stabilize the marine soft clay under submerged conditions.In order to solve this problem,the enhancement of cement-stabilized marine soft clay was investigated in this study by adding the ionic soil stabilizer(ISS)and polyacrylamide(PAM).For this purpose,varying contents of ISS and PAM(ISS-P)were added into cement-stabilized marine soft clay and subjected to curing under submerged conditions.Atterberg limits tests,direct shear tests,unconfined compression strength(UCS)tests,water-stability tests,scanning electron microscopy analysis,and X-ray diffraction analysis were carried out.The results show that using 1.8%ISS and 0.9%PAM as the optimal ratio,the cohesion,internal friction angle,UCS,and water-stability of the samples increased by 182.7%,15.4%,176.5%,and 368.5% compared to the cement-stabilized soft clay after 28 d.The increment in soil cohesion with increasing ISS-P content was more apparent than that in the internal friction angle.The combined action of ion exchange attraction and electrostatic adsorption altered the failure characteristics of the samples,resulting in localized micro-cracking and multiple failure paths.Increasing the content of ISS-P strengthened the skeletal structure of soil,reduced inter-particle spacing,and enhanced the water-stability.Additionally,ISS promotes the hydration of cement and compensates for the inhibitory effect of PAM on early cement hydration.ISS-P can effectively enhance the strength and stability of submerged cement-based stabilized marine soft clay.展开更多
MgH_(2) has been extensively studied as one of the most ideal solid hydrogen storage materials.Nevertheless,rapid capacity decay and sluggish hydrogen storage kinetics hamper its practical application.Herein,a Ni/C na...MgH_(2) has been extensively studied as one of the most ideal solid hydrogen storage materials.Nevertheless,rapid capacity decay and sluggish hydrogen storage kinetics hamper its practical application.Herein,a Ni/C nano-catalyst doped MgH_(2)(MgH_(2)–Ni/C)shows an improved hydrogen absorption kinetics with largely reduced activation energy.Particularly,the MgH_(2)–Ni/C displays remarkable cycling stability,which maintains a high capacity of 6.01 wt.%(98.8%of initial capacity)even after 50 full hydrogen ab/desorption cycles,while the undoped MgH_(2) counterpart retains only 85.2%of its initial capacity.Detailed microstructure characterizations clearly reveal that particle sintering/growth accounts primarily for the deterioration of cycling performance of undoped MgH_(2).By comparison,MgH_(2)–Ni/C can maintain a stable particle size with a growing porous structure during long-term cycling,which effectively increases the specific surface of the particles.A novel carbon-induced-porosity stabilization mechanism is proposed,which can stabilize the proportion of rapid hydrogen absorption process,thus dominating the excellent cycling performance of MgH_(2)–Ni/C.This study provides new insights into the cycling stability mechanism of carbon-containing Mg-based hydrogen storage materials,thus promoting their practical applications.展开更多
Ni-rich LiNi0.8Mn0.1Co0.1O2(NCM)cathodes in layered oxide cathodes are attractive for high-energy lithium-ion batteries but suffer from rapid capacity fade and thermal instability at high charge voltages.In this study...Ni-rich LiNi0.8Mn0.1Co0.1O2(NCM)cathodes in layered oxide cathodes are attractive for high-energy lithium-ion batteries but suffer from rapid capacity fade and thermal instability at high charge voltages.In this study,we propose an entropy-assisted multi-element doping strategy to mitigate these issues.Specifically,two routes are designed and compared:bulk-like localized high-entropy doping(BHE-NCM)and surface-distributed high-entropy-zone doping(SHE-NCM).The surface entropy-doped NCM cathode delivers enhanced electrochemical performance,including higher capacity retention under 4.5 V cycling and superior rate capability,compared to both bulk-like and pristine counterparts.Comprehensive material characterization reveals that surface-localized doping stabilizes the layered structure with reduced microcrack formation and creates a uniform dopant-rich surface region with improved thermal and electrochemical stability.Overall,entropy-assisted doping at the near surface zone effectively alleviates structural degradation and interface reactions in Ni-rich NCM,enabling improved cycling performance at high voltage.This work highlights the significance of surface entropy engineering as a promising strategy for designing high-voltage cathodes with improved safety and longevity.展开更多
基金the National Natural Science Foundation of China(Grant Nos.42177163 and 42071080)the China Postdoctoral Science Foundation(Grant No.2022M723347).
文摘Due to the limited hydration capacity,solidification/stabilization(S/S)with waste concrete powder(WCP)has a low strength.Carbonation can reduce carbon dioxide(CO_(2))emissions and improve strength of lead-contaminated soil,but its mechanism and environmental behaviors are unclear.In light of this,a comprehensive study was conducted on the compressive strength,lead immobilization,conductivity characteristics,and carbonation mechanism of carbonated Pb-contaminated soils stabilized with WCP compared to calcining 600℃WCP.Results indicated that with carbonation,the compressive strength of the samples was significantly improved at the early stage(1 d),resulting in increased unconfined compressive strength(UCS)by 2.5-5.2 times due to the filling of pores by calcite.It negatively affected the lead immobilization capacity of highly doped(30%)samples,while this effect reversed after 3 d of carbonating due to the reduced alkaline environment.The lead immobilization capacity decreased after 28 d of carbonating due to the cracking of samples and the influence of a lower pH on the solubility of lead-carbonated hydroxide((PbCO_(3))_(2)Pb(OH)_(2)).The water evaporation(saturation<16.8%)led to dry shrinkage cracking and decreased UCS of the samples.Based on this finding,a conductivity model was developed for carbonated and cured samples,accurately predicting changes in saturation levels(R^(2)=0.98).A relationship between conductivity and UCS or lead immobilization capacity was proposed.This research proposed an innovative method for the reduction of CO_(2)emission as well as laid down a theoretical basis for the recovery of WCP and lead-contaminated soils through carbonation.
文摘Amino acids are the building blocks of proteins and play vital roles in both biological systems and drug development.In recent years,increasing attention has been given to the functionalization of amino acid derivatives.Since the introduction of therapeutic insulin in the early 20th century,the conjugation of drug molecules with amino acids and peptides has been pivotal in driving advancements in drug discovery and become an integral part of modern medical practice.Currently,over a hundred peptide-drug conjugates have received global approval and are widely used to treat diseases such as diabetes,cancer,chronic pain,and multiple sclerosis.Key technologies for conjugating peptides with bioactive molecules include antibody-drug conjugates(ADCs),peptide-drug conjugates(PDCs),and proteolysis targeting chimeras(PROTACs).Significant efforts have been dedicated to developing strategies for the modification of amino acids and peptides,with particular focus on site-selective C-H alkylation/arylation reactions.These reactions are crucial for synthesizing bioactive molecules,as they enable the precise introduction of functional groups at specific positions,thereby improving the pharmacological properties of the resulting compounds.
基金supported by Fundamental Research Funds for the Central Universities(2023KYJD1008)the Science Research Projects of the Anhui Higher Education Institutions of China(2022AH051582).
文摘Reversible solid oxide cell(RSOC)is a new energy conversion device with significant applications,especially for power grid peaking shaving.However,the reversible conversion process of power generation/energy storage poses challenges for the performance and stability of air electrodes.In this work,a novel high-entropy perovskite oxide La_(0.2)Pr_(0.2)Gd_(0.2)Sm_(0.2)Sr_(0.2)Co_(0.8)Fe_(0.2)O_(3−δ)(HE-LSCF)is proposed and investigated as an air electrode in RSOC.The electrochemical behavior of HE-LSCF was studied as an air electrode in both fuel cell and electrolysis modes.The polarization impedance(Rp)of the HE-LSCF electrode is only 0.25Ω·cm^(2) at 800℃ in an air atmosphere.Notably,at an electrolytic voltage of 2 V and a temperature of 800℃,the current density reaches up to 1.68 A/cm^(2).The HE-LSCF air electrode exhibited excellent reversibility and stability,and its electrochemical performance remains stable after 100 h of reversible operation.With these advantages,HE-LSCF is shown to be an excellent air electrode for RSOC.
基金supported by the Shenyang Municipal Science and Technology Project,China(23-409-2-03)the Liaoning Provincial Department of Science and Technology Project,China(Z20230183)the Liaoning Provincial Applied Basic Research Program,China(2022JH2/101300173).
文摘Both soil organic carbon (SOC) and iron (Fe) oxide content, among other factors, drive the formation and stability of soil aggregates.However, the mechanism of these drivers in greenhouse soil fertilized with organic fertilizer is not well understood.In a 3-year field experiment, we aimed to investigate the factors which drive the stability of soil aggregates in greenhouse soil.To explore the impact of organic fertilizer on soil aggregates, we established four treatments:no fertilization (CK);inorganic fertilizer (CF);organic fertilizer (OF);and combined application of inorganic and organic fertilizers(COF).The application of organic fertilizer significantly enhanced the stability of aggregates, that is it enhanced the mean weight diameter, geometric mean diameter and aggregate content (%) of>0.25 mm aggregate fractions.OF and COF treatments increased the concentration of SOC, especially the aliphatic-C, aromatic-C and polysaccharide-C components of SOC, particularly in>0.25 mm aggregates.Organic fertilizer application significantly increased the content of free Fe(Fed), reactive Fe (Feo), and non-crystalline Fe in both bulk soil and aggregates.Furthermore, non-crystalline Fe showed a positive correlation with SOC content in both bulk soil and aggregates.Both non-crystalline Fe and SOC were significantly positively correlated with>2 mm mean weight diameter.Overall, we believe that the increase of SOC, aromatic-C, and non-crystal ine Fe concentrations in soil after the application of organic fertilizer is the reason for improving soil aggregate stability.
基金the W.M.Keck Center for Nano-Scale Imaging in the Department of Chemistry and Biochemistry at the University of Arizona(Grant No.RRID:SCR_022884),with funding from the W.M.Keck Foundation Grant.
文摘Approximately 3.44 billion tons of copper mine tailings(MT)were produced globally in 2018 with an increase of 45%from 2010.Significant efforts are being made to manage these tailings through storage facilities,recycling,and reuse in different industries.Currently,a large portion of tailings are managed through the tailing storage facilities(TSF)where these tailings undergo hydro-thermal-mechanical stresses with seasonal cycles which are not comprehensively understood.This study presents an investigative study to evaluate the performance of control and cement-stabilized copper MT under the influence of seasonal cycles,freeze-thaw(F-T)and wet-dry(W-D)conditions,representing the seasonal variability in the cold and arid regions.The control and cement-stabilized MT samples were subjected to a maximum of 12 F-T and 12 W-D cycles and corresponding micro-and-macro behavior was investigated through scanning electron microscope(SEM),volumetric strain(εvT,wet density(r),moisture content loss,and unconfined compressive strength(UCS)tests.The results indicated the vulnerability of Copper MT to 67%and 75%strength loss reaching residual states with 12 F-T and 8 W-D cycles,respectively.Whereas the stabilized MT retained 39%-55%and 16%-34%strength with F-T and W-D cycles,demonstrating increased durability.This research highlights the impact of seasonal cycles and corresponding strength-deformation characteristics of control and stabilized Copper MT in cold and arid regions.
基金supported by the National Natural Science Foundation of China (41977020)the China Agriculture Research System of MOF and MARA (CARS22)。
文摘oil aggregates profoundly impact soil sustainability and crop productivity, and they are influenced by complexinteractions between minerals and organics. This study aimed to elucidate the alterations in mineralogy and soilorganic carbon(SOC) following long-term green manure incorporation and the effect on soil aggregates. Based on 5-and 36-year field experiments, surface soil samples(0–20 cm) were collected from Alfisol and Ferrisol soilssubjected to rice–rice–winter fallow(CK) and rice–rice–Chinese milk vetch(MV) treatments to investigate aggregatestability, mineralogy, SOC composition, and soil microstructural characteristics. The results showed that high clay-content Ferrisol exhibited greater aggregate stability than low clay-content Alfisol. The phyllosilicates in Alfisolprimarily comprised illite and vermiculite, whereas those in Ferrisol with high-content free-form Fe oxides(Fed) weredominated by kaolinite. Additionally, the clay fraction in Ferrisol contained more aromatic-C than the clay fraction inAlfisol. The 36-year MV incorporation significantly increased the Ferrisol macroaggregate stability(9.57–13.37%),and it also facilitated the transformation of vermiculite into kaolinite and significantly increased the clay, Fed, and aromatic-C contents in Ferrisol. Backscattered electron(BSE)-scanning electron microscopy/energy dispersive X-ray spectroscopy(SEM/EDS) revealed a compact aggregate structure in Ferrisol with co-localization of Feoxides and kaolinite. Moreover, the partial least path model(PLS-PM) revealed that clay content directly improvedmacroaggregate stability, and that kaolinite and Fed positively and directly affected clay or indirectly modulated clay formation by increasing the aromatic-C levels. Overall, long-term MV incorporation promotes clay aggregation by affecting mineral transformation to produce more kaolinite and Fe oxides and retain aromatic-C, and it ultimately improves aggregate stability.
基金financially supported by the National Natural Science Foundation of China(Grant No.52074331).
文摘Wellbore instability is one of the significant challenges in the drilling engineering and during the development of carbonate reservoirs,especially with open-hole completion.The problems of wellbore instability such as downhole collapse and silt deposit in the fractured carbonate reservoir of Tarim Basin(Ordovician)are severe.Solid destabilization and production(SDP)was proposed to describe this engineering problem of carbonate reservoirs.To clarify the mechanism and mitigate potential borehole instability problems,we conducted particle size distribution(PSD)analysis,X-ray diffraction(XRD)analysis,triaxial compression tests,and micro-scale sand production tests based on data analysis.We found that the rock fragments and silt in the wellbore came from two sources:one from the wellbore collapse in the upper unplugged layers and the other from the production of sand particles carried by the fluid in the productive layers.Based on the experimental study,a novel method combining a geomechanical model and microscopic sand production model was proposed to predict wellbore instability and analyze its influencing factors.The critical condition and failure zone predicted by the prediction model fit well with the field observations.According to the prediction results,the management and prevention measures of wellbore instability in carbonate reservoirs were proposed.It is suggested to optimize the well track in new drilling wells while upgrading the production system in old wells.This study is of great guiding significance for the optimization of carbonate solid control and it improves the understanding of the sand production problems in carbonate reservoirs.
文摘Photothermal catalytic methane dry reforming(DRM)technology can convert greenhouse gases(i.e.CH_(4)and CO_(2))into syngas(i.e.H_(2)and CO),providing more opportunities for reducing the greenhouse effect and achieving carbon neutrality.In the DRM field,Ni-based catalysts attract wide attention due to their low cost and high activity.However,the carbon deposition over Ni-based catalysts always leads to rapid deactivation,which is still a main challenge.To improve the long-term stability of Ni-based catalysts,this work proposes a carbon-atom-diffusion strategy under photothermal conditions and investigates its effect on a Zn-doped Ni-based photothermal catalyst(Ni_(3)Zn@CeO_(2)).The photothermal catalytic behavior of Ni_(3)Zn@CeO_(2)can maintain more than 70 h in DRM reaction.And the photocatalytic DRM activity of Ni_(3)Zn@CeO_(2)is 1.2 times higher than thermal catalytic activity.Density functional theory(DFT)calculation and experimental characterizations indicate that Ni_(3)Zn promotes the diffusion of carbon atoms into the Ni_(3)Zn to form the Ni_(3)ZnC0.7 phase with body-centered cubic(bcc)structure,thus inhibiting carbon deposition.Further,in-situ diffuse reflectance infrared Fourier transform(DRIFT)spectroscopy and DFT calculation prove Ni_(3)Zn@CeO_(2)benefits the CH_(4)activation and inhibits the carbon deposition during the DRM process.Through inducing carbon atoms diffusion within the Ni_(3)Zn lattice,this work provides a straightforward and feasible strategy for achieving efficient photothermal catalytic DRM and even other CH_(4)conversion implementations with long-term stability.
基金supported by the National Key Research and Development Program of China(2022YFB2502103)the Xiamen Science and Technology Project(No.3502Z20231057)+2 种基金the National Natural Science Foundation of China(No.22288102,No.22279107,No.22309153)the Fujian Provincial Natural Science Foundation of China(No.2024J01040)the Fundamental Research Funds for the Central Universities(No.20720230039)。
文摘Extending the charging voltage of LiCoO_(2)(LCO)is an ongoing and promising approach to increase its energy density.However,the main challenge of the approach lies in the insuperable cathodic interfacial processes at high voltage,which leads to rapid failure both in the performance and structure of the LCO cathode.Herein,a Li_(2)CO_(3)-based additive was prepared by a simple sand-milling method,enabling a low electrochemical decomposition voltage<4.6 V from commonly>4.8 V,stabilizing the interface of the LCO cathode at 4.6 V.The decomposition of Li_(2)CO_(3)provides extra Li^(+)and CO_(2)to supplement the Li consumption required in the initial irreversible interfacial reactions and rapidly form a uniform and stable cathode electrolyte interphase layer(less organic and more inorganic components)on the LCO cathode by reducing CO_(2).Thus,the phase transformation and the emergence of high-valent Co ions on the surface of LCO at 4.6 V high voltage were inhibited.Thanks to this,with 2%Li_(2)CO_(3)-based additive,the capacity retention of commercial LCO at a high voltage of 4.6 V at 0.5 C for 100 cycles was improved from 59.3%to 79.3%.This work improves the high-voltage stability of LCO and provides a new idea for realizing the high-voltage operation of batteries.
基金Funded by the Natural Science Foundation of Hebei Province(No.E2020209010)the Science and Technology Plan Project of Tangshan(No.19150225E)the Key R&D Projects of North China University of Science and Technology(No.ZD-ST-202301)。
文摘In view of the volume instability of steel slag aggregate leading to the quality problem of expansion damage in asphalt road construction,the 4.75-9.5 mm steel slag particles were treated by autoclaved carbonation technology,and the effects of the carbonation system(temperature and time)on the autoclaved pulverization rate,f-CaO content,and the relationship between them for the carbonated steel slag were investigated.In addition,the microstructure of the carbonated steel slag was analyzed by X-ray diffractometer(XRD),scanning electron microscope and energy dispersive spectrometer(SEM-EDS),metallographic microscope and X-ray fluorescence imaging spectrometer(XRF).The experimental results indicate that,under the initial CO_(2)pressure of 1.0 MPa,increasing the carbonation temperature leads to the increase in the crystal plane spacing of Ca(OH)_(2)that was generated by the hydration of minerals in steel slag,and promotes the transformation of carbonated CaCO_(3)from the orthorhombic system to the hexagonal system,resulting in the increase of the crystal planes spacing of them,meantime,accelerates the decomposition of RO phases and also the outward migration of Ca^(2+),Fe^(2+),and Mn^(2+)ions to cover and coat on the Si^(4+),Al^(3+)ions,and impels the formation of hydroxides such as Fe(OH)_(3)and the formation of carbonates such as Ca(Mg)CO_(3),FeCO_(3)and MnCO_(3).Carbonation at the temperature of 90℃for 3 h can reach the center of 4.75-9.5 mm steel slag particles.Meanwhile,the increase of temperature can promote the mineral reaction in steel slag,resulting in the fuzzy interface between mineral phases,increase of burrs,dispersion,crossover,reduction of grain size,and rearrangement of mineral particles.
基金supported by the National Natural Science Foundation of China(Nos.42222102,41971136,and 42171107)the Jilin Provincial Department of Science and Technology,China(No.20230508089RC)the Professional Association of the Alliance of International Science Organizations(No.ANSO-PA-2020-14).
文摘Global climate change exerts profound effects on snow cover,with consequential impacts on microbial activities and the stability of soil organic carbon(SOC)within aggregates.Northern peatlands are significant carbon reservoirs,playing a critical role in mitigating climate change.However,the effects of snow variations on microbial-mediated SOC stability within aggregates in peatlands remain inadequately understood.Here,an in-situ field experiment manipulating snow conditions(i.e.,snow removal and snow cover)was conducted to investigate how snow variations affect soil microbial community and the associated SOC stability within soil aggregates(>2,0.25-2,and<0.25 mm)in a peatland of Northeast China.The results showed that snow removal significantly increased the SOC content and stability within aggregates.Compared to the soils with snow cover,snow removal resulted in decreased soil average temperatures in the topsoil(0-30 cm depth)and subsoil(30-60 cm depth)(by 1.48 and 1.34°C,respectively)and increased freeze-thaw cycles(by 11 cycles),consequently decreasing the stability of aggregates in the topsoil and subsoil(by 23.68%and 6.85%,respectively).Furthermore,more recalcitrant carbon and enhanced SOC stability were present in microaggregates(<0.25 mm)at two soil depths.Moreover,reductions in bacterial diversity and network stability were observed in response to snow removal.Structural equation modeling analysis demonstrated that snow removal indirectly promoted(P<0.01)SOC stability by regulating carbon to nitrogen(C:N)ratio within aggregates.Overall,our study suggested that microaggregate protection and an appropriate C:N ratio enhanced carbon sequestration in response to climate change.
基金National Key R&D Program of China,Grant/Award Number:2023YFB2503900National Natural Science Foundation of China,Grant/Award Number:12172143Shenzhen Science and Technology Program,Grant/Award Numbers:JCYJ20220818100418040,JCYJ20220530160816038。
文摘Constructing silicon(Si)-based composite electrodes that possess high energy density,long cycle life,and fast charging capability simultaneously is critical for the development of high performance lithium-ion batteries for mitigating range anxiety and slow charging issues in new energy vehicles.Herein,a thick silicon/carbon composite electrode with vertically aligned channels in the thickness direction(VC-SC)is constructed by employing a bubble formation method.Both experimental characterizations and theoretical simulations confirm that the obtained vertical channel structure can effectively address the problem of sluggish ion transport caused by high tortuosity in conventional thick electrodes,conspicuously enhance reaction kinetics,reduce polarization and side reactions,mitigate stress,increase the utilization of active materials,and promote cycling stability of the thick electrode.Consequently,when paired with LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)(NCM622),the VC-SC||NCM622 pouch type full cell(~6.0 mAh cm^(-2))exhibits significantly improved rate performance and capacity retention compared with the SC||NCM622 full cell with the conventional silicon/carbon composite electrode without channels(SC)as the anode.The assembled VC-SC||NCM622 pouch full cell with a high energy density of 490.3 Wh kg^(-1)also reveals a remarkable fast charging capability at a high current density of 2.0 mA cm^(-2),with a capacity retention of 72.0%after 500 cycles.
基金supported by the National Key R&D Program of China(Grant No.2022YFC3901204)the Foundation for Distinguished Young Scholars of Hubei Province,China(Grant No.2021CFA096)the National Natural Science Foundation of China(Grant No.U20A20320).
文摘Evaluating the stabilized lead(Pb)-contaminated soils through sampling and laboratory testing involves costly and time-consuming processes.Therefore,this study employed a low-cost and non-destructive resistivity tool to evaluate the Pb-contaminated soils stabilized by electrolytic manganese residue(EMR)-based geopolymer(EG-OPC)from the strength and environmental benefits perspective.First,unconfined compressive strength(UCS)and leaching tests were conducted to study the stabilization effectiveness of EG-OPC.Results indicated that the UCS values of soil(5000 mg/kg of pollutants)stabilized by 20%EG-OPC were 4.87 MPa and 8.13 MPa after 7 d and 60 d of curing,respectively.After 60 d of curing,the Pb concentration in the leachate reached 44 mg/L,far lower than the control group(321 mg/L).Second,soil,pore water,and leachate resistivity(ERS,ERW,and ERL)were measured to establish fitting relationships with strength parameters and pollution risk.The good fitting results(e.g.ERS/ERW versus UCS/secant modulus(E50):correlation coefficient R2 z 0.9,ERS/ERW versus Pb contents:R2 z 0.9,and ERL versus Pb2þconcentration:R2¼0.92)and well used Archie's law(ERS versus ERW:R2>0.9)indicate that the resistivity can be used to evaluate the stabilization effectiveness.Furthermore,the microscopic results revealed two behaviors,demonstrating the reliability of resistivity:(1)with the hydration process,resistivity increases due to a denser structure and lower amounts of free water and Pb ions,and(2)the addition of Pb reduces resistivity due to its inhibition or even destructive effects on cementation and formation of hydration products.
文摘Carbon fibres have been produced from hydroxypropyl-modified lignin(TcC)/bio-based polyamide 1010(PA1010)blended filaments.Two grades of PA1010,with different molecular weights and rheological properties,were used for blending with TcC.An oxidative thermal stabilisation step was used prior to carbonisation in an inert atmosphere to prevent the fusion of the filaments during the latter step.Thermal stabilisation was not possible using a one-step stabilisation process reported in the literature for lignin and other lignin/synthetic polymer blends.As a consequence,a cyclic process involving an additional isothermal phase at a lower temperature than the precursor filaments’melting point,was introduced to increase the cross-linking reactions between the lignin and polyamide.Thermally stabilised filaments were characterised by DSC,TGA,TGA-FTIR,ATR,and SEM techniques.Polymer rheology and heating rate used during thermal stabilisation influenced the thermal stabilisation process and mechanical properties of the derived filaments.Thermally stabilised filaments using optimised conditions(heating in the air atmosphere at 0.25℃/min to 180℃;isothermal for 1 h,cooling back down to ambient at 5℃/min;heating to 250℃ at 0.25℃/min,isothermal for 2 h)could be successfully carbonised.Carbon fibres pro-duced had void-free morphologies and mechanical properties comparable to similarly thermally stabilised and carbonised polyacrylonitrile(PAN)filaments.
文摘It is economical to perform methane and carbon dioxide reforming(DRM)under industrially relevant high-pressure conditions,but the harsh operation condition poses a grand challenge for coke-resistant catalyst design.Here,we propose to boost the coke-tolerance of Co catalyst by applying a contact potential introduced by immiscible Ag clusters.We demonstrate that Co clusters separated by neighboring Ag on Yttria-stabilized zirconia(YSZ)support can serve as a coke-and sintering-resistant DRM catalyst under diluent gas-free,stoichiometric CH_(4) and CO_(2) feeding,1123 K and 20 bar.Since immiscible metals are ubiquitous and metal contact influences surface work function in general,this new design concept may have general implications for tailoring catalytic properties of metals.
基金Project(2021H0028) supported by the Natural Scienceof Fujian Province,ChinaProject(JAT200455) supported by the Fujian Provincial Young and Middle-aged Teacher Education Project,ChinaProject(fma2023003) supported by the Open Fund of Fujian Provincial Key Laboratory of Functional Materials and Applications,China。
文摘Rich-nickel layered ternary NCM811 has been widely used in the field of electric vehicles ascribed to its high theoretical specific capacity.However,poor cycling stability and rate-performance hindered its further development.Herein,different amounts of nitrogen-doped carbon were wrapped on the surface of NCM811 via a facile rheological phase method by regulating the amount of dopamine hydrochloride.The effects of the coating amounts on the structure and electrochemical performance are investigated.The DFT calculation,XRD,SEM and XPS reveal that an appropriate amount of nitrogen-doped carbon coating could uniformly form a protective layer on the NCM811 surface and the introduced N could anchor Ni atoms to inhibit the Li^(+)/Ni^(2+)mixing,but excessive amount would reduce Ni^(3+)to Ni^(2+)so as to conversely aggravate Li^(+)/Ni^(2+)mixing.Among the samples,the NCM811-CN0.75 sample exhibits the most excellent electrochemical performance,delivering a high-rate capacity of 151.6 mA·h/g at 10C,and long-term cyclability with 82.2%capacity retention after 300 cycles at 5C,exhibiting remarkable rate-performance and cyclability.
基金the financial support from Innovative Research Group Project of Natural Science Foundation of Hebei Province(No.E2022209093)Central Guidance Local Science and Technology Development Fund Project of Hebei Province(No.236Z3803G)+1 种基金Scientific and Technological Project of Tangshan(No.23130205E)Youth Teacher Pre Research Fund Project of the School of Metallurgy and Energy(No.YJY20244373).
文摘A slurry-phase carbonation technique was utilized,employing argon oxygen decarburization slag(AOD slag)as a source of calcium and MgCl_(2) as a regulator for the crystal morphology of acicular aragonite.Subsequently,the carbonated AOD slag,enriched with acicular aragonite,was employed in fabricating composite cementitious materials,followed by an analysis of their evolution in hydration heat,hydration products,and microscopic morphology.Additionally,it delved into the mechanism through which acicular aragonite enhances the stength of composite cementitious materials.Moreover,advanced simulation software for engineering and sciences(ABAQUS)was utilized to simulate the compressive performance of composite mortar with varying dosages of acicular aragonite.The findings demonstrate that the carbonated AOD slag,containing 83.4%acicular aragonite(with an average aspect ratio of 21.31),exhibited commendable compatibility with cement.Moderate integration of carbonated AOD slag facilitated the formation of calcium sulfoaluminate hydrate(AFt)phases.The acicular aragonite within the cementitious matrix showcased remarkable filling effects.As the dosage of carbonated AOD slag increased,flexural and compressive strengths of cement mortar initially rose before declining.Upon reaching a 6%cement inclusion of carbonated AOD slag,the various constituents of the cementitious material displayed optimal synergy.The numerical simulation results confirmed the experimental findings,demonstrating a favorable increase in compressive strength and flexural strength with the addition of acicular aragonite.The acicular aragonite strengthened the matrix by serving bridging and pull-out functions.
基金supported by the Fundamental Research Funds for the Central Universities(Nos.202061027,202261063)the National Natural Science Foundation of China(No.41572247)。
文摘The traditional cement-based stabilization cannot effectively stabilize the marine soft clay under submerged conditions.In order to solve this problem,the enhancement of cement-stabilized marine soft clay was investigated in this study by adding the ionic soil stabilizer(ISS)and polyacrylamide(PAM).For this purpose,varying contents of ISS and PAM(ISS-P)were added into cement-stabilized marine soft clay and subjected to curing under submerged conditions.Atterberg limits tests,direct shear tests,unconfined compression strength(UCS)tests,water-stability tests,scanning electron microscopy analysis,and X-ray diffraction analysis were carried out.The results show that using 1.8%ISS and 0.9%PAM as the optimal ratio,the cohesion,internal friction angle,UCS,and water-stability of the samples increased by 182.7%,15.4%,176.5%,and 368.5% compared to the cement-stabilized soft clay after 28 d.The increment in soil cohesion with increasing ISS-P content was more apparent than that in the internal friction angle.The combined action of ion exchange attraction and electrostatic adsorption altered the failure characteristics of the samples,resulting in localized micro-cracking and multiple failure paths.Increasing the content of ISS-P strengthened the skeletal structure of soil,reduced inter-particle spacing,and enhanced the water-stability.Additionally,ISS promotes the hydration of cement and compensates for the inhibitory effect of PAM on early cement hydration.ISS-P can effectively enhance the strength and stability of submerged cement-based stabilized marine soft clay.
基金supported by the National Natural Science Foundation of China(Nos.22279111,51971195,and 11935004)the Natural Science Foundation of Hebei Province(No.B2020203037)Subsidy for Hebei Key Laboratory of Applied Chemistry after Operation Performance(No.22567616H).
文摘MgH_(2) has been extensively studied as one of the most ideal solid hydrogen storage materials.Nevertheless,rapid capacity decay and sluggish hydrogen storage kinetics hamper its practical application.Herein,a Ni/C nano-catalyst doped MgH_(2)(MgH_(2)–Ni/C)shows an improved hydrogen absorption kinetics with largely reduced activation energy.Particularly,the MgH_(2)–Ni/C displays remarkable cycling stability,which maintains a high capacity of 6.01 wt.%(98.8%of initial capacity)even after 50 full hydrogen ab/desorption cycles,while the undoped MgH_(2) counterpart retains only 85.2%of its initial capacity.Detailed microstructure characterizations clearly reveal that particle sintering/growth accounts primarily for the deterioration of cycling performance of undoped MgH_(2).By comparison,MgH_(2)–Ni/C can maintain a stable particle size with a growing porous structure during long-term cycling,which effectively increases the specific surface of the particles.A novel carbon-induced-porosity stabilization mechanism is proposed,which can stabilize the proportion of rapid hydrogen absorption process,thus dominating the excellent cycling performance of MgH_(2)–Ni/C.This study provides new insights into the cycling stability mechanism of carbon-containing Mg-based hydrogen storage materials,thus promoting their practical applications.
基金supported by the Australian Research Council via Discovery Projects(Nos.DP200103315,DP200103332 and DP230100685)Linkage Projects(No.LP220200920)+1 种基金support from the IONTOF M6 ToF-SIMS(funded by ARC LIEF,LE190100053)the Kratos Axis Ultra XPS(ARC LIEF,LE120100026)。
文摘Ni-rich LiNi0.8Mn0.1Co0.1O2(NCM)cathodes in layered oxide cathodes are attractive for high-energy lithium-ion batteries but suffer from rapid capacity fade and thermal instability at high charge voltages.In this study,we propose an entropy-assisted multi-element doping strategy to mitigate these issues.Specifically,two routes are designed and compared:bulk-like localized high-entropy doping(BHE-NCM)and surface-distributed high-entropy-zone doping(SHE-NCM).The surface entropy-doped NCM cathode delivers enhanced electrochemical performance,including higher capacity retention under 4.5 V cycling and superior rate capability,compared to both bulk-like and pristine counterparts.Comprehensive material characterization reveals that surface-localized doping stabilizes the layered structure with reduced microcrack formation and creates a uniform dopant-rich surface region with improved thermal and electrochemical stability.Overall,entropy-assisted doping at the near surface zone effectively alleviates structural degradation and interface reactions in Ni-rich NCM,enabling improved cycling performance at high voltage.This work highlights the significance of surface entropy engineering as a promising strategy for designing high-voltage cathodes with improved safety and longevity.
