Efficient lubrication of magnesium alloys is a highly challenging topic in the field of tribology.In this study,magnesium silicate hydroxide(MSH)nanotubes with serpentine structures were synthesized.The tribological b...Efficient lubrication of magnesium alloys is a highly challenging topic in the field of tribology.In this study,magnesium silicate hydroxide(MSH)nanotubes with serpentine structures were synthesized.The tribological behavior of AZ91D magnesium alloy rubbed against GCr15 steel was studied under lubricating oil with surface-modified MSH nanotubes as additives.The effects of the concentration,applied load,and reciprocating frequency on the friction and wear of the AZ91D alloy were studied using an SRV-4 sliding wear tester.Results show a decrease of 18.7–68.5%in friction coefficient,and a reduction of 19.4–54.3%in wear volume of magnesium alloy can be achieved by applying the synthetic serpentine additive under different conditions.A suspension containing 0.3 wt.%MSH was most efficient in reducing wear and friction.High frequency and medium load were more conducive to improving the tribological properties of magnesium alloys.A series of beneficial physical and chemical processes occurring at the AZ91D alloy/steel interface can be used to explain friction and wear reduction based on the characterization of the morphology,chemical composition,chemical state,microstructure,and nanomechanical properties of the worn surface.The synthetic MSH,with serpentine structure and nanotube morphology,possesses excellent adsorbability,high chemical activity,and good self-lubrication and catalytic activity.Therefore,physical polishing,tribochemical reactions,and physicalchemical depositions can occur easily on the sliding contacts.A dense tribolayer with a complex composition and composite structure was formed on the worn surface.Its high hardness,good toughness and plasticity,and prominent lubricity resulted in the improvement of friction and wear,making the synthetic MSH a promising efficient oil additive for magnesium alloys under boundary and mixed lubrication.展开更多
This study aims to develop a chloride diffusion simulation method that considers the hydration microstructure and pore solution properties during the hydration of tricalcium silicate(C3S).The method combines the hydra...This study aims to develop a chloride diffusion simulation method that considers the hydration microstructure and pore solution properties during the hydration of tricalcium silicate(C3S).The method combines the hydration simulation,thermodynamic calculation,and finite element analysis to examine the effects of pore solution,including effect of electrochemical potential,effect of chemical activity,and effect of mechanical interactions between ions,on the chloride effective diffusion coefficient of hydrated C3S paste.The results indicate that the effect of electrochemical potential on chloride diffusion becomes stronger with increasing hydration age due to the increase in the content of hydrated calcium silicate;as the hydration age increases,the effect of chemical activity on chloride diffusion weakens when the number of diffusible elements decreases;the effect of mechanical interactions between ions on chloride diffusion decreases with the increase of hydration age.展开更多
Sm^(3+)-doped materials exhibit red and orange emissions in the visible light region,showing broad applica⁃tion prospects in both laser and display material fields.However,the inherent small emission and absorption cr...Sm^(3+)-doped materials exhibit red and orange emissions in the visible light region,showing broad applica⁃tion prospects in both laser and display material fields.However,the inherent small emission and absorption cross-sections of Sm^(3+)result in low luminous efficiency,posing challenges for achieving high-quality solid-state lighting.Here,the excellent white emission of Sm^(3+)doped lithium aluminum silicate(LAS)glass was realized by introducing the Ag aggregates through Ag ion exchange.Under 395 nm excitation,the Ag-doped samples exhibit significant fluo⁃rescence enhancement with color coordinates close to the equal energy white point E(0.33,0.33)and a color ren⁃dering index(CRI)of 81.8.The study reveals that the surface plasmon resonance(SPR)effect of Ag nanoparticles enhances the luminescence of Sm^(3+),while the energy transfer mechanism between Ag^(+)and Sm^(3+)also promotes fluores⁃cence enhancement.By adjusting the concentration of AgNO_(3) and the exchange time,a series of high-quality full-spectrum white light emissions were obtained,indicating that the Ag ion-exchanged Sm^(3+)-doped LAS glass has good application potential in the development of solid-state lighting devices.Moreover,variations in the excitation wave⁃length can effectively tune the emission color,further demonstrating the tunability and practicality of this material in optoelectronic applications.展开更多
An in-depth understanding of the hydration mechanism of tricalcium silicate is an important basis for optimizing cement strength development.In this study,the adsorption of water molecules onto the M3-C3S(001)surface ...An in-depth understanding of the hydration mechanism of tricalcium silicate is an important basis for optimizing cement strength development.In this study,the adsorption of water molecules onto the M3-C3S(001)surface at different water coverage levels(θ=1/5,2/5,3/5,4/5,and 1)was investigated using first-principles calculations.The results demonstrate that the conclusions obtained for single water molecule adsorption cannot be fully applied to multiple water molecule adsorption.The total adsorption energies become more negative with increasing water coverage,while the average adsorption energy of each water molecule becomes more positive with increasing water coverage.The water–water interactions reduce the water–surface interactions and are responsible for the anticooperative adsorption of multiple water molecules onto M3-C_(3)S(001).The formation of Ca–OH(–Ca)bonds favors the detachment of Ca from co-valent oxygen,which reveals the significant role of dissociative adsorption.This work aims to extend the water adsorption study on M3-C3S(001)from single water molecule adsorption to multiple water molecule adsorption,providing more detailed insights into the initial water reaction on the C3S surface.展开更多
Heavy metal-contaminated sites are primarily treated via solidification and adsorption.Calcium silicate hydrate(C-S-H)is generated during the soil stabilization process and contributes significantly to the strength an...Heavy metal-contaminated sites are primarily treated via solidification and adsorption.Calcium silicate hydrate(C-S-H)is generated during the soil stabilization process and contributes significantly to the strength and durability of the stabilized soil.To understand how the soil moisture content and heavy metal concentration affect the transport of heavy metals and the tensile strength of C-S-H,this study performed molecular dynamics(MD)simulations under different moisture and concentration levels.The results showed that Pb2+presented the highest adsorption to the surface of C-S-H due to its strong electrostatic interaction energy.The adsorption density peaks of Pb2+were 1.5–5 times greater than those of Cd2+and Zn2+.Zn2+and Cd2+ions were more likely to be adsorbed onto water molecules and form a larger hydrated radius than Pb2+.The adsorption of heavy metals onto C-S-H initially increased as the metal concentration increased and then decreased because of the limited sorption sites on C-S-H.The diffusion coefficients of the multicomponent metals in C-S-H showed no consistent trends.The maximum tensile strength of C-S-H decreased with increasing soil moisture and heavy metal concentrations.The tensile stress increased approximately linearly with strain until it reached a peak,after which it gradually declined but remained above zero,indicating good ductility and toughness under unsaturated conditions.These findings offer valuable molecular insights into the interactions between C-S-H and heavy metals and soil moisture,thereby advancing our understanding of their combined effects on soil stabilization.展开更多
To clarify the precipitation of silica hydrate from the real desilication solutions of aluminosilicate solid wastes by adding seeds and improve integrated waste utilization,the seeded precipitation was studied using s...To clarify the precipitation of silica hydrate from the real desilication solutions of aluminosilicate solid wastes by adding seeds and improve integrated waste utilization,the seeded precipitation was studied using synthesized sodium silicate solution containing different inorganic salt impurities.The results show that sodium chloride,sodium sulfate,sodium carbonate,or calcium chloride can change the siloxy group structure.The number of high-polymeric siloxy groups decreases with increasing sodium chloride or sodium sulfate concentration,which is detrimental to seeded precipitation.Calcium chloride favors the polymerization of silicate ions,and even the chain groups precipitate with the precipitation of high-polymeric sheet and cage-like siloxy groups.The introduced sodium cations in sodium carbonate render a more open network structure of high-polymeric siloxy groups,although the carbonate ions favor the polymerization of siloxy groups.No matter how the four impurities affect the siloxy group structure,the precipitates are always amorphous opal-A silica hydrate.展开更多
An inorganic potassium silicate coating with pigments of alumina,aluminum phosphate,NiCrAlY and copper chromite black was prepared on CB2 stainless steel.Oxidation behavior in either ambient air or O_(2)+H_(2) O mixtu...An inorganic potassium silicate coating with pigments of alumina,aluminum phosphate,NiCrAlY and copper chromite black was prepared on CB2 stainless steel.Oxidation behavior in either ambient air or O_(2)+H_(2) O mixture at 630℃ for 2000 h was comparatively studied,and the coating exhibited excellent resistance under both test conditions.The water vapor considerably accelerated the oxidation of the uncoated CB2 steel,as the hydroxide,the main constituent of the coating,had a negligible evaporation rate at test temperature,while it had a limited effect on the coated sample.Meanwhile,the existence of coating may prolong or eliminate the incubation period in the O_(2)+H_(2) O mixture at 630℃.After oxidation,the coating matrix is in an amorphous state and fillers as alumina and copper chromite black are stable in the coating.Leucite(KAlSi_(2) O_(6))formed by Al from NiCrAlY and potassium silicate in the coatings was detected after tests either in O_(2) or O_(2)+H_(2) O mixture.展开更多
The time-dependent viscoelastic response of cement-based materials to applied deformation is far from fully understood at the atomic level.Calcium silicate hydrate(C-S-H),the main hydration product of Portland cement,...The time-dependent viscoelastic response of cement-based materials to applied deformation is far from fully understood at the atomic level.Calcium silicate hydrate(C-S-H),the main hydration product of Portland cement,is responsible for the viscoelastic mechanism of cement-based materials.In this study,a molecular model of C-S-H was developed to explain the stress relaxation characteristics of C-S-H at different initial deformation states,Ca/Si ratios,temperatures,and water contents,which cannot be accessed experimentally.The stress relaxation of C-S-H occurs regardless of whether it is subjected to initial shear,tensile,or compressive deformation,and shows a heterogeneous characteristic.Water plays a crucial role in the stress relaxation process.A large Ca/Si ratio and high temperature reduce the cohesion between the calcium-silicate layer and the interlayer region,and the viscosity of the interlayer region,thereby accelerating the stress relaxation of C-S-H.The effect of the hydrogen bond network and the morphology of C-S-H on the evolution of the stress relaxation characteristics of C-S-H at different water contents was elucidated by nonaffine mean squared displacement.Our results shed light on the stress relaxation characteristics of C-S-H from a microscopic perspective,bridging the gap between the microscopic phenomena and the underlying atomic-level mechanisms.展开更多
Phosphor-converted near-infrared light-emitting diodes(NIR pc-LEDs) are finding applications in various fields including food quality analysis,biomedical imaging,night vision,and biomedicine.The crucial factor in the ...Phosphor-converted near-infrared light-emitting diodes(NIR pc-LEDs) are finding applications in various fields including food quality analysis,biomedical imaging,night vision,and biomedicine.The crucial factor in the development of NIR pc-LEDs devices lies in the advancement of high-performance broadband NIR phosphors,In this work,novel Cr^(3+)-activated silicate phosphors NaRESi_(3)O_(9)(RE=Y,Lu,Sc) are reported.This silicate has a special 3D network structure in which RE has four different sites,forming four octahedrons and providing suitable occupation sites for Cr^(3+).The phosphors demonstrate a wide emission spectrum ranging from 750 to 1450 nm when excited by light at 468 nm.The full width at half maximum(FWHM),which benefits from the presence of Cr^(3+)ions occupying multiple sites,is measured to be 203 nm.Notably,the strongest emission peak is observed at a longer wavelength of 984 nm compared to most other systems activated by Cr^(3+).The Na_(3)ScSi_(3)O_(9) lattice provides a weak crystal field(Dq/B=1.97) and weak phonon-photon coupling for Cr^(3+),and the integrated emission intensity of Na_(3)ScSi_(3)O_(9):0,03Cr^(3+)is 4.66 times stronger than that of Na_(3)YSi_(3)O_(9):0.03Cr^(3+).展开更多
Solid-state batteries with solid polymer electrolytes are considered the most promising due to their high energy density and safety advantages.However,their development is hindered by the limitations of polymer electr...Solid-state batteries with solid polymer electrolytes are considered the most promising due to their high energy density and safety advantages.However,their development is hindered by the limitations of polymer electrolytes,such as low ionic conductivity,poor mechanical strength and inadequate fire resistance.This study presents a thin polyvinylidene fluoride-based composite solid electrolyte film(25μm incorporating twodimensional modified lipophilic lithium magnesium silicate(LLS)as additives with good dispersibility.The incorporation of LLS promotes grain refinement in polyvinylidene fluoride(PVDF),enhances the densification of electrolyte films,increases the tensile strength to10.42 MPa and the elongation to 251.58%,improves ion transport interfac e,and facilitates uniform deposition of lithium ions.Furthermore,LLS demonstrates strong adsorption ability,promoting the formation of solvated molecules,resulting in high ionic conductivity(2.07×10^(-4)S·cm^(-1)at 30℃)and a stable lithium/electrolyte interface.Symmetric Li//Li cells assembled with the thin composite electrolytes exhibit stable cycling for2000 h at 0.1 mA·cm^(-2)and 0.05 mAh·cm^(-2).Additionally,the LiFePO_(4)//Li battery shows a capacity retention rate of99.9%after 200 cycles at 0.5C and room temperature.展开更多
Inhibitors are important for flotation separation of quartz and feldspar.In this study,a novel combined inhibitor was used to separate quartz and feldspar in near-neutral pulp.Selective inhibition of the combined inhi...Inhibitors are important for flotation separation of quartz and feldspar.In this study,a novel combined inhibitor was used to separate quartz and feldspar in near-neutral pulp.Selective inhibition of the combined inhibitor was assessed by micro-flotation experiments.And a series of detection methods were used to detect differences in the surface properties of feldspars and quartz after flotation reagents and put forward the synergistic strengthening mechanism.The outcomes were pointed out that pre-mixing combined inhibitors were more effective than the addition of Ca^(2+)and SS in sequence under the optimal proportion of 1:5.A concentrate from artificial mixed minerals that was characterized by a high quartz grade and a high recovery was acquired,and was found to be 90.70wt% and 83.70%,respectively.It was demonstrated that the combined inhibitor selectively prevented the action of the collector and feldspar from Fourier-transform infrared(FT-IR)and adsorption capacity tests.The results of X-ray photoelectron spectroscopy(XPS)indicated that Ca^(2+)directly interacts with the surface of quartz to increase the adsorption of collectors.In contrast,the chemistry property of Al on the feldspar surface was altered by combined inhibitor due to Na^(+)and Ca^(2+)taking the place of K^(+),resulting in the composite inhibitor forms a hydrophilic structure,which prevents the adsorption of the collector on the surface of feldspar by interacting with the Al active site.The combination of Ca^(2+)and SS synergically strengthens the difference of collecting property between quartz and feldspar by collector,thus achieving the effect of efficient separation.A new strategy for flotation to separate quartz from feldspar in near-neutral pulp was provided.展开更多
This study investigated the leaching of scandium from a Sc-bearing silicate ore.The Sc concentrate obtained by beneficiation pre-enrichment has 1.03×10^(−4) wt%Sc and 14.66 wt%Fe.The main Sc-bearing minerals are ...This study investigated the leaching of scandium from a Sc-bearing silicate ore.The Sc concentrate obtained by beneficiation pre-enrichment has 1.03×10^(−4) wt%Sc and 14.66 wt%Fe.The main Sc-bearing minerals are limonite,chlorite,sericite,and hornblende,in the form of isomorphism.High-pressure leaching(HPL)with sulfuric acid(98 wt%)and NaF was used to dispose this samples.The Sc leaching efficiency of 91.82%was obtained under the optimum conditions,which are pressure of 5.0×10^(5) Pa,A/O value of 1.1,L/S value of 1.8,NaF dosage of 2 wt%,at 130℃ for 6 h.The X-ray diffraction(XRD)and scanning electron microscopy(SEM)results show that the residue is mainly quartz phase in the multihole shape.Compared with ordinary leaching for silicate,high-pressure leaching has significant advantages in saving acid and energy consumption.展开更多
The strength development law of γ-type dicalcium silicate (γ-C_(2)S) under different carbonation processes was investigated,and the carbonation mechanism of γ-C_(2)S under the action of NH_(4)HCO_(3) was clarified ...The strength development law of γ-type dicalcium silicate (γ-C_(2)S) under different carbonation processes was investigated,and the carbonation mechanism of γ-C_(2)S under the action of NH_(4)HCO_(3) was clarified by using a wide range of test methods,including XRD and SEM.A method of saturated NH_(4)HCO_(3) solution as a curing agent was identified to improve the carbonation efficiency and enhance the carbonation degree of γ-C_(2)S,and then a high-strength carbonated specimen was obtained.Microhardness analysis and SEM morphology analysis were conducted on the carbonised specimens obtained under atmospheric pressure carbonisation conditions using the curing agent.It was found that γ-C_(2)S could perform carbonisation well under atmospheric pressure,which promoted the carbonisation efficiency and decreased the carbonisation cost simultaneously.Therefore,a new carbonisation process solution was proposed for the rapid carbonisation of γ-C_(2)S.展开更多
Currently a technique widely used for gold extraction is mercury by amalgamation technique, the tailing produced pollutes water of all kinds, so it is necessary to develop a form of selective mitigation, for which it ...Currently a technique widely used for gold extraction is mercury by amalgamation technique, the tailing produced pollutes water of all kinds, so it is necessary to develop a form of selective mitigation, for which it is necessary to use complexing agents based on calixarene functionalized with mercury sequestering agents. These are immobilized by adding supports based on natural silica to form polymers and make them insoluble in all types of solvents, so that they can be used as an extractor and at the same time regenerate to their original properties for continuous reuse.展开更多
The influence of sodium silicate on the corrosion behaviour of aluminium alloy 7075-T6 in 0.1 M sodium chloride solution was studied by open circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) tec...The influence of sodium silicate on the corrosion behaviour of aluminium alloy 7075-T6 in 0.1 M sodium chloride solution was studied by open circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) techniques. Scanning electron microscopy (SEM) was used to characterize the AA7075-T6 surface. Silicate can significantly reduce corrosion deterioration and the inhibition efficiency increases with the concentration of Na<sub>2</sub>SiO<sub>3</sub>. The corrosion inhibition mechanism involves the formation of a protective film over the alloy surface by adsorption of aluminosilicate anions from solution, as has also been suggested by others in literature.展开更多
The paper overviews the research and application of silicate plugging agent, according to the different mechanisms and application forms, the plugging agent is divided into silicate gel, silicate precipitation, silica...The paper overviews the research and application of silicate plugging agent, according to the different mechanisms and application forms, the plugging agent is divided into silicate gel, silicate precipitation, silicate/polymer, silicate/surfactant, silicate gel/foam and so on. This paper chiefly introduces the conception, mechanism and development tendency of the different systems mentioned above. The development tendency manifests as fully utilize personal properties and cooperate with other plugging agents or technologies, including the study of reaction mechanism, combination of plugging agent, grasping water flood timing, developing deep profile control and water shutoff technology, combining with other measures (chemicals huff and puff), in order to play the role of such blocking agents, further enhance oil recovery.展开更多
The adsorption isotherm of sodium polyacrylate on dicalcium silicate（2CaO-SiO2） in sodium aluminate solution at 80 ℃ was studied.The type of surface adsorption of sodium polyacrylate is saturated adsorption,and the...The adsorption isotherm of sodium polyacrylate on dicalcium silicate（2CaO-SiO2） in sodium aluminate solution at 80 ℃ was studied.The type of surface adsorption of sodium polyacrylate is saturated adsorption,and the adsorption behavior belongs to L-type,according with the monolayer adsorption model of Langmuir equation.The surface coverage of sodium polyacrylate is 1.06 mol/μm2.The relation curve between the surface pressure and the molecular area of adsorption film was obtained by Gibbs formula.The variation of interfacial energy caused by adsorption as well as the relationship between the relation curve and the type of adsorption was discussed.展开更多
The leaching kinetics of zinc silicate in ammonium chloride solution was investigated. The effects of stirring speed （150？400 r/min）, leaching temperature （95-108 ℃, particle size of zinc silicate （61-150 μm...The leaching kinetics of zinc silicate in ammonium chloride solution was investigated. The effects of stirring speed （150？400 r/min）, leaching temperature （95-108 ℃, particle size of zinc silicate （61-150 μm） and the concentration of ammonium chloride （3.5-5.5 mol/L） on leaching rate of zinc were studied. The results show that decreasing the particle size of zinc silicate and increasing the leaching temperature and concentration of ammonium chloride can obviously enhance the leaching rate of zinc. Among the kinetic models of the porous solids tested, the grain model with porous diffusion control can well describe the zinc leaching kinetics. The apparent activation energy of the leaching reaction is 161.26 kJ/mol and the reaction order with respect to ammonium chloride is 3.5.展开更多
Silicate sol post-treatment was applied to form a complete composite coating on the phosphated zinc layer. The chemical compositions of the coatings were investigated using XPS. The coated samples were firstly scratch...Silicate sol post-treatment was applied to form a complete composite coating on the phosphated zinc layer. The chemical compositions of the coatings were investigated using XPS. The coated samples were firstly scratched and then exposed to the neutral salt spray(NSS) chamber for different time. The microstructure and chemical compositions of the scratches were studied using SEM and EDS. And the non-scratched coated samples were compared. The self-healing mechanism of the composite coatings was discussed. The results show that during corrosion, the self-healing ions in composite coatings dissolve, diffuse and transfer to the scratches or the defects, and then recombine with Zn2+ to form insoluble compound, which deposits and covers the exposed zinc. The corrosion products on the scratches contain silicon, phosphorous, oxygen, chloride and zinc, and they are compact, fine, needle and flake, effectively inhibiting the corrosion formation and expansion of the exposed zinc layer. The composite coatings have good self-healing ability.展开更多
The influences of sodium silicate on manganese electrodeposition in sulfate solution were investigated. Manganese electrodeposition experiments indicate that a certain amount of sodium silicate can improve cathode cur...The influences of sodium silicate on manganese electrodeposition in sulfate solution were investigated. Manganese electrodeposition experiments indicate that a certain amount of sodium silicate can improve cathode current efficiency and initial pH 7.0?8.0 is the optimized pH for high cathode current efficiency. The analyses of scanning electron microscopy (SEM) and X-ray diffraction (XRD) indicate the compact morphology and nanocrystalline structure of electrodeposits. X-ray photoelectron spectrometry (XPS) analysis shows that the elements of Mn, Si and O exist in the deposit. The solution chemistry calculations of sulfate electrolyte and sodium silicate solution indicate that species of Mn2+, MnSO4, Mn(SO4)2?2 , Mn2+, MnSiO3, Mn(NH3)2+, SiO32?and HSiO3? are the main active species during the process of manganese electrodeposition. The reaction trend between Mn2+ and Si-containing ions is confirmed by the thermodynamic analysis. In addition, polarization curve tests confirm that sodium silicate can increase the overpotential of hydrogen evolution reaction, and then indirectly improve the cathode current efficiency.展开更多
基金support from the National Natural Science Foundation of China(grant number 52075544)Innovation Funds of Jihua Laboratory(X220971UZ230)+1 种基金Basic and Applied Basic Research Foundation of Guangdong Province(2022A1515110649)Funds from Research Platforms of Guangdong Higher Education Institutes(2022ZDJS038).
文摘Efficient lubrication of magnesium alloys is a highly challenging topic in the field of tribology.In this study,magnesium silicate hydroxide(MSH)nanotubes with serpentine structures were synthesized.The tribological behavior of AZ91D magnesium alloy rubbed against GCr15 steel was studied under lubricating oil with surface-modified MSH nanotubes as additives.The effects of the concentration,applied load,and reciprocating frequency on the friction and wear of the AZ91D alloy were studied using an SRV-4 sliding wear tester.Results show a decrease of 18.7–68.5%in friction coefficient,and a reduction of 19.4–54.3%in wear volume of magnesium alloy can be achieved by applying the synthetic serpentine additive under different conditions.A suspension containing 0.3 wt.%MSH was most efficient in reducing wear and friction.High frequency and medium load were more conducive to improving the tribological properties of magnesium alloys.A series of beneficial physical and chemical processes occurring at the AZ91D alloy/steel interface can be used to explain friction and wear reduction based on the characterization of the morphology,chemical composition,chemical state,microstructure,and nanomechanical properties of the worn surface.The synthetic MSH,with serpentine structure and nanotube morphology,possesses excellent adsorbability,high chemical activity,and good self-lubrication and catalytic activity.Therefore,physical polishing,tribochemical reactions,and physicalchemical depositions can occur easily on the sliding contacts.A dense tribolayer with a complex composition and composite structure was formed on the worn surface.Its high hardness,good toughness and plasticity,and prominent lubricity resulted in the improvement of friction and wear,making the synthetic MSH a promising efficient oil additive for magnesium alloys under boundary and mixed lubrication.
基金Funded by the Natural Science Foundation of Jiangsu Province(No.BK20241529)China Postdoctoral Science Foundation(No.2024M750736)。
文摘This study aims to develop a chloride diffusion simulation method that considers the hydration microstructure and pore solution properties during the hydration of tricalcium silicate(C3S).The method combines the hydration simulation,thermodynamic calculation,and finite element analysis to examine the effects of pore solution,including effect of electrochemical potential,effect of chemical activity,and effect of mechanical interactions between ions,on the chloride effective diffusion coefficient of hydrated C3S paste.The results indicate that the effect of electrochemical potential on chloride diffusion becomes stronger with increasing hydration age due to the increase in the content of hydrated calcium silicate;as the hydration age increases,the effect of chemical activity on chloride diffusion weakens when the number of diffusible elements decreases;the effect of mechanical interactions between ions on chloride diffusion decreases with the increase of hydration age.
文摘Sm^(3+)-doped materials exhibit red and orange emissions in the visible light region,showing broad applica⁃tion prospects in both laser and display material fields.However,the inherent small emission and absorption cross-sections of Sm^(3+)result in low luminous efficiency,posing challenges for achieving high-quality solid-state lighting.Here,the excellent white emission of Sm^(3+)doped lithium aluminum silicate(LAS)glass was realized by introducing the Ag aggregates through Ag ion exchange.Under 395 nm excitation,the Ag-doped samples exhibit significant fluo⁃rescence enhancement with color coordinates close to the equal energy white point E(0.33,0.33)and a color ren⁃dering index(CRI)of 81.8.The study reveals that the surface plasmon resonance(SPR)effect of Ag nanoparticles enhances the luminescence of Sm^(3+),while the energy transfer mechanism between Ag^(+)and Sm^(3+)also promotes fluores⁃cence enhancement.By adjusting the concentration of AgNO_(3) and the exchange time,a series of high-quality full-spectrum white light emissions were obtained,indicating that the Ag ion-exchanged Sm^(3+)-doped LAS glass has good application potential in the development of solid-state lighting devices.Moreover,variations in the excitation wave⁃length can effectively tune the emission color,further demonstrating the tunability and practicality of this material in optoelectronic applications.
基金supported by the Young Elite Scientists Sponsorship Program by CAST(No.2023QNRC001)Natural Science Foundation of Hunan Province,China(No.2024JJ2074)supported in part by the High Performance Computing Center of Central South University,China and the Pawsey Supercomputing Centre with funding from the Australian Government and the Government of Western Australia.
文摘An in-depth understanding of the hydration mechanism of tricalcium silicate is an important basis for optimizing cement strength development.In this study,the adsorption of water molecules onto the M3-C3S(001)surface at different water coverage levels(θ=1/5,2/5,3/5,4/5,and 1)was investigated using first-principles calculations.The results demonstrate that the conclusions obtained for single water molecule adsorption cannot be fully applied to multiple water molecule adsorption.The total adsorption energies become more negative with increasing water coverage,while the average adsorption energy of each water molecule becomes more positive with increasing water coverage.The water–water interactions reduce the water–surface interactions and are responsible for the anticooperative adsorption of multiple water molecules onto M3-C_(3)S(001).The formation of Ca–OH(–Ca)bonds favors the detachment of Ca from co-valent oxygen,which reveals the significant role of dissociative adsorption.This work aims to extend the water adsorption study on M3-C3S(001)from single water molecule adsorption to multiple water molecule adsorption,providing more detailed insights into the initial water reaction on the C3S surface.
基金supported by the National Natural Science Foundation of China(Grant Nos.42030710 and 52308345)the National Key Research and Development Program of China(Grant No.2023YFC3707903).
文摘Heavy metal-contaminated sites are primarily treated via solidification and adsorption.Calcium silicate hydrate(C-S-H)is generated during the soil stabilization process and contributes significantly to the strength and durability of the stabilized soil.To understand how the soil moisture content and heavy metal concentration affect the transport of heavy metals and the tensile strength of C-S-H,this study performed molecular dynamics(MD)simulations under different moisture and concentration levels.The results showed that Pb2+presented the highest adsorption to the surface of C-S-H due to its strong electrostatic interaction energy.The adsorption density peaks of Pb2+were 1.5–5 times greater than those of Cd2+and Zn2+.Zn2+and Cd2+ions were more likely to be adsorbed onto water molecules and form a larger hydrated radius than Pb2+.The adsorption of heavy metals onto C-S-H initially increased as the metal concentration increased and then decreased because of the limited sorption sites on C-S-H.The diffusion coefficients of the multicomponent metals in C-S-H showed no consistent trends.The maximum tensile strength of C-S-H decreased with increasing soil moisture and heavy metal concentrations.The tensile stress increased approximately linearly with strain until it reached a peak,after which it gradually declined but remained above zero,indicating good ductility and toughness under unsaturated conditions.These findings offer valuable molecular insights into the interactions between C-S-H and heavy metals and soil moisture,thereby advancing our understanding of their combined effects on soil stabilization.
基金financial support from the National Natural Science Foundation of China(No.52074364)。
文摘To clarify the precipitation of silica hydrate from the real desilication solutions of aluminosilicate solid wastes by adding seeds and improve integrated waste utilization,the seeded precipitation was studied using synthesized sodium silicate solution containing different inorganic salt impurities.The results show that sodium chloride,sodium sulfate,sodium carbonate,or calcium chloride can change the siloxy group structure.The number of high-polymeric siloxy groups decreases with increasing sodium chloride or sodium sulfate concentration,which is detrimental to seeded precipitation.Calcium chloride favors the polymerization of silicate ions,and even the chain groups precipitate with the precipitation of high-polymeric sheet and cage-like siloxy groups.The introduced sodium cations in sodium carbonate render a more open network structure of high-polymeric siloxy groups,although the carbonate ions favor the polymerization of siloxy groups.No matter how the four impurities affect the siloxy group structure,the precipitates are always amorphous opal-A silica hydrate.
基金financially supported by the National Natural Science Foundation of China(No.52001142).
文摘An inorganic potassium silicate coating with pigments of alumina,aluminum phosphate,NiCrAlY and copper chromite black was prepared on CB2 stainless steel.Oxidation behavior in either ambient air or O_(2)+H_(2) O mixture at 630℃ for 2000 h was comparatively studied,and the coating exhibited excellent resistance under both test conditions.The water vapor considerably accelerated the oxidation of the uncoated CB2 steel,as the hydroxide,the main constituent of the coating,had a negligible evaporation rate at test temperature,while it had a limited effect on the coated sample.Meanwhile,the existence of coating may prolong or eliminate the incubation period in the O_(2)+H_(2) O mixture at 630℃.After oxidation,the coating matrix is in an amorphous state and fillers as alumina and copper chromite black are stable in the coating.Leucite(KAlSi_(2) O_(6))formed by Al from NiCrAlY and potassium silicate in the coatings was detected after tests either in O_(2) or O_(2)+H_(2) O mixture.
基金This work is supported by the National Natural Science Foundation of China(Nos.51602229 and U2040222)the Opening Project of Key Laboratory of Advanced Civil Engineering Materials of Ministry of Education(Tongji University)the Water Conservancy Science and Technology Project of Hunan Province(No.XSKJ2021000-15),China.
文摘The time-dependent viscoelastic response of cement-based materials to applied deformation is far from fully understood at the atomic level.Calcium silicate hydrate(C-S-H),the main hydration product of Portland cement,is responsible for the viscoelastic mechanism of cement-based materials.In this study,a molecular model of C-S-H was developed to explain the stress relaxation characteristics of C-S-H at different initial deformation states,Ca/Si ratios,temperatures,and water contents,which cannot be accessed experimentally.The stress relaxation of C-S-H occurs regardless of whether it is subjected to initial shear,tensile,or compressive deformation,and shows a heterogeneous characteristic.Water plays a crucial role in the stress relaxation process.A large Ca/Si ratio and high temperature reduce the cohesion between the calcium-silicate layer and the interlayer region,and the viscosity of the interlayer region,thereby accelerating the stress relaxation of C-S-H.The effect of the hydrogen bond network and the morphology of C-S-H on the evolution of the stress relaxation characteristics of C-S-H at different water contents was elucidated by nonaffine mean squared displacement.Our results shed light on the stress relaxation characteristics of C-S-H from a microscopic perspective,bridging the gap between the microscopic phenomena and the underlying atomic-level mechanisms.
基金supported by the Natural Science Foundation of The Educational Department of Liaoning Province (JYTMS20231627)the Natural Science Foundation of Liaoning Province (2020-MS-286)。
文摘Phosphor-converted near-infrared light-emitting diodes(NIR pc-LEDs) are finding applications in various fields including food quality analysis,biomedical imaging,night vision,and biomedicine.The crucial factor in the development of NIR pc-LEDs devices lies in the advancement of high-performance broadband NIR phosphors,In this work,novel Cr^(3+)-activated silicate phosphors NaRESi_(3)O_(9)(RE=Y,Lu,Sc) are reported.This silicate has a special 3D network structure in which RE has four different sites,forming four octahedrons and providing suitable occupation sites for Cr^(3+).The phosphors demonstrate a wide emission spectrum ranging from 750 to 1450 nm when excited by light at 468 nm.The full width at half maximum(FWHM),which benefits from the presence of Cr^(3+)ions occupying multiple sites,is measured to be 203 nm.Notably,the strongest emission peak is observed at a longer wavelength of 984 nm compared to most other systems activated by Cr^(3+).The Na_(3)ScSi_(3)O_(9) lattice provides a weak crystal field(Dq/B=1.97) and weak phonon-photon coupling for Cr^(3+),and the integrated emission intensity of Na_(3)ScSi_(3)O_(9):0,03Cr^(3+)is 4.66 times stronger than that of Na_(3)YSi_(3)O_(9):0.03Cr^(3+).
基金financially supported by the National Key R&D Program of China(No.2023YFB2503801)the Key Program of the National Natural Science Foundation of China(No.52231009)+1 种基金the National Science Foundation of China(No.52302253)the Key R&D Program of Hubei Province(No.2023BAB028)。
文摘Solid-state batteries with solid polymer electrolytes are considered the most promising due to their high energy density and safety advantages.However,their development is hindered by the limitations of polymer electrolytes,such as low ionic conductivity,poor mechanical strength and inadequate fire resistance.This study presents a thin polyvinylidene fluoride-based composite solid electrolyte film(25μm incorporating twodimensional modified lipophilic lithium magnesium silicate(LLS)as additives with good dispersibility.The incorporation of LLS promotes grain refinement in polyvinylidene fluoride(PVDF),enhances the densification of electrolyte films,increases the tensile strength to10.42 MPa and the elongation to 251.58%,improves ion transport interfac e,and facilitates uniform deposition of lithium ions.Furthermore,LLS demonstrates strong adsorption ability,promoting the formation of solvated molecules,resulting in high ionic conductivity(2.07×10^(-4)S·cm^(-1)at 30℃)and a stable lithium/electrolyte interface.Symmetric Li//Li cells assembled with the thin composite electrolytes exhibit stable cycling for2000 h at 0.1 mA·cm^(-2)and 0.05 mAh·cm^(-2).Additionally,the LiFePO_(4)//Li battery shows a capacity retention rate of99.9%after 200 cycles at 0.5C and room temperature.
基金the financial support from the National Key Research and Development Program of China(No.2018YFC1903403)Young Elite Scientists Sponsorship Program by CAST(No.2022QNRC001).
文摘Inhibitors are important for flotation separation of quartz and feldspar.In this study,a novel combined inhibitor was used to separate quartz and feldspar in near-neutral pulp.Selective inhibition of the combined inhibitor was assessed by micro-flotation experiments.And a series of detection methods were used to detect differences in the surface properties of feldspars and quartz after flotation reagents and put forward the synergistic strengthening mechanism.The outcomes were pointed out that pre-mixing combined inhibitors were more effective than the addition of Ca^(2+)and SS in sequence under the optimal proportion of 1:5.A concentrate from artificial mixed minerals that was characterized by a high quartz grade and a high recovery was acquired,and was found to be 90.70wt% and 83.70%,respectively.It was demonstrated that the combined inhibitor selectively prevented the action of the collector and feldspar from Fourier-transform infrared(FT-IR)and adsorption capacity tests.The results of X-ray photoelectron spectroscopy(XPS)indicated that Ca^(2+)directly interacts with the surface of quartz to increase the adsorption of collectors.In contrast,the chemistry property of Al on the feldspar surface was altered by combined inhibitor due to Na^(+)and Ca^(2+)taking the place of K^(+),resulting in the composite inhibitor forms a hydrophilic structure,which prevents the adsorption of the collector on the surface of feldspar by interacting with the Al active site.The combination of Ca^(2+)and SS synergically strengthens the difference of collecting property between quartz and feldspar by collector,thus achieving the effect of efficient separation.A new strategy for flotation to separate quartz from feldspar in near-neutral pulp was provided.
基金Project supported by Yunnan Province Basic Research Program(202101AT070141)。
文摘This study investigated the leaching of scandium from a Sc-bearing silicate ore.The Sc concentrate obtained by beneficiation pre-enrichment has 1.03×10^(−4) wt%Sc and 14.66 wt%Fe.The main Sc-bearing minerals are limonite,chlorite,sericite,and hornblende,in the form of isomorphism.High-pressure leaching(HPL)with sulfuric acid(98 wt%)and NaF was used to dispose this samples.The Sc leaching efficiency of 91.82%was obtained under the optimum conditions,which are pressure of 5.0×10^(5) Pa,A/O value of 1.1,L/S value of 1.8,NaF dosage of 2 wt%,at 130℃ for 6 h.The X-ray diffraction(XRD)and scanning electron microscopy(SEM)results show that the residue is mainly quartz phase in the multihole shape.Compared with ordinary leaching for silicate,high-pressure leaching has significant advantages in saving acid and energy consumption.
基金Funded by Hubei Technology Innovation Key Program (No.2018AAA004)。
文摘The strength development law of γ-type dicalcium silicate (γ-C_(2)S) under different carbonation processes was investigated,and the carbonation mechanism of γ-C_(2)S under the action of NH_(4)HCO_(3) was clarified by using a wide range of test methods,including XRD and SEM.A method of saturated NH_(4)HCO_(3) solution as a curing agent was identified to improve the carbonation efficiency and enhance the carbonation degree of γ-C_(2)S,and then a high-strength carbonated specimen was obtained.Microhardness analysis and SEM morphology analysis were conducted on the carbonised specimens obtained under atmospheric pressure carbonisation conditions using the curing agent.It was found that γ-C_(2)S could perform carbonisation well under atmospheric pressure,which promoted the carbonisation efficiency and decreased the carbonisation cost simultaneously.Therefore,a new carbonisation process solution was proposed for the rapid carbonisation of γ-C_(2)S.
文摘Currently a technique widely used for gold extraction is mercury by amalgamation technique, the tailing produced pollutes water of all kinds, so it is necessary to develop a form of selective mitigation, for which it is necessary to use complexing agents based on calixarene functionalized with mercury sequestering agents. These are immobilized by adding supports based on natural silica to form polymers and make them insoluble in all types of solvents, so that they can be used as an extractor and at the same time regenerate to their original properties for continuous reuse.
文摘The influence of sodium silicate on the corrosion behaviour of aluminium alloy 7075-T6 in 0.1 M sodium chloride solution was studied by open circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) techniques. Scanning electron microscopy (SEM) was used to characterize the AA7075-T6 surface. Silicate can significantly reduce corrosion deterioration and the inhibition efficiency increases with the concentration of Na<sub>2</sub>SiO<sub>3</sub>. The corrosion inhibition mechanism involves the formation of a protective film over the alloy surface by adsorption of aluminosilicate anions from solution, as has also been suggested by others in literature.
文摘The paper overviews the research and application of silicate plugging agent, according to the different mechanisms and application forms, the plugging agent is divided into silicate gel, silicate precipitation, silicate/polymer, silicate/surfactant, silicate gel/foam and so on. This paper chiefly introduces the conception, mechanism and development tendency of the different systems mentioned above. The development tendency manifests as fully utilize personal properties and cooperate with other plugging agents or technologies, including the study of reaction mechanism, combination of plugging agent, grasping water flood timing, developing deep profile control and water shutoff technology, combining with other measures (chemicals huff and puff), in order to play the role of such blocking agents, further enhance oil recovery.
基金Project(50974036)supported by the National Natural Science Foundation of China
文摘The adsorption isotherm of sodium polyacrylate on dicalcium silicate（2CaO-SiO2） in sodium aluminate solution at 80 ℃ was studied.The type of surface adsorption of sodium polyacrylate is saturated adsorption,and the adsorption behavior belongs to L-type,according with the monolayer adsorption model of Langmuir equation.The surface coverage of sodium polyacrylate is 1.06 mol/μm2.The relation curve between the surface pressure and the molecular area of adsorption film was obtained by Gibbs formula.The variation of interfacial energy caused by adsorption as well as the relationship between the relation curve and the type of adsorption was discussed.
基金Project(2014CB643404)supported by the National Basic Research Program of ChinaProject(51374254)supported by the National Natural Science Foundation of China
文摘The leaching kinetics of zinc silicate in ammonium chloride solution was investigated. The effects of stirring speed （150？400 r/min）, leaching temperature （95-108 ℃, particle size of zinc silicate （61-150 μm） and the concentration of ammonium chloride （3.5-5.5 mol/L） on leaching rate of zinc were studied. The results show that decreasing the particle size of zinc silicate and increasing the leaching temperature and concentration of ammonium chloride can obviously enhance the leaching rate of zinc. Among the kinetic models of the porous solids tested, the grain model with porous diffusion control can well describe the zinc leaching kinetics. The apparent activation energy of the leaching reaction is 161.26 kJ/mol and the reaction order with respect to ammonium chloride is 3.5.
基金Project(2012J05099)supported by the Natural Science Foundation of Fujian Province,ChinaProject(YKJ10021R)supported by the Scientific Research Project of Xiamen University of Technology
文摘Silicate sol post-treatment was applied to form a complete composite coating on the phosphated zinc layer. The chemical compositions of the coatings were investigated using XPS. The coated samples were firstly scratched and then exposed to the neutral salt spray(NSS) chamber for different time. The microstructure and chemical compositions of the scratches were studied using SEM and EDS. And the non-scratched coated samples were compared. The self-healing mechanism of the composite coatings was discussed. The results show that during corrosion, the self-healing ions in composite coatings dissolve, diffuse and transfer to the scratches or the defects, and then recombine with Zn2+ to form insoluble compound, which deposits and covers the exposed zinc. The corrosion products on the scratches contain silicon, phosphorous, oxygen, chloride and zinc, and they are compact, fine, needle and flake, effectively inhibiting the corrosion formation and expansion of the exposed zinc layer. The composite coatings have good self-healing ability.
基金Project(2015BAB17B01)supported by the National Science and Technology Support Program of ChinaProject(21376273)supported by the National Natural Science Foundation of China
文摘The influences of sodium silicate on manganese electrodeposition in sulfate solution were investigated. Manganese electrodeposition experiments indicate that a certain amount of sodium silicate can improve cathode current efficiency and initial pH 7.0?8.0 is the optimized pH for high cathode current efficiency. The analyses of scanning electron microscopy (SEM) and X-ray diffraction (XRD) indicate the compact morphology and nanocrystalline structure of electrodeposits. X-ray photoelectron spectrometry (XPS) analysis shows that the elements of Mn, Si and O exist in the deposit. The solution chemistry calculations of sulfate electrolyte and sodium silicate solution indicate that species of Mn2+, MnSO4, Mn(SO4)2?2 , Mn2+, MnSiO3, Mn(NH3)2+, SiO32?and HSiO3? are the main active species during the process of manganese electrodeposition. The reaction trend between Mn2+ and Si-containing ions is confirmed by the thermodynamic analysis. In addition, polarization curve tests confirm that sodium silicate can increase the overpotential of hydrogen evolution reaction, and then indirectly improve the cathode current efficiency.
