In this study,Mg O was partially used as an alkali source in the peroxide bleaching process of bleached chemi-thermomechanical pulp(BCTMP).The effects of substitution percentage of Mg O for Na OH on the bulk,optical,a...In this study,Mg O was partially used as an alkali source in the peroxide bleaching process of bleached chemi-thermomechanical pulp(BCTMP).The effects of substitution percentage of Mg O for Na OH on the bulk,optical,and physical properties of bleached pulp,and the main effluent characteristics were analyzed.In addition,the influencing mechanism of Mgbased alkali on the strength properties of the BCTMP was further investigated.Strength properties of the BCTMPs were investigated as a function of charge characteristics,fiber morphology,surface lignin content,relative bonding area,and hydrogen bonds of the BCTMP.The results showed that cationic demand(CD) and chemical oxygen demand(COD_(Cr)) of the bleaching effluent decreased as the substitution percentage of Mg O for Na OH increased; meanwhile,the bulk and optical properties of the BCTMP increased.Nevertheless,the strength properties(tensile,tear,and burst indices) of the bleached pulp decreased as the substitution percentage of Mg O for Na OH increased.The decrease in the fiber charge density and increase in the surface lignin content affected the fiber swelling,resulting in a decline in pulp interfibers bonding strength and further loss of the tensile and burst indices.展开更多
To address the challenges posed by high reaction temperatures and the slow kinetics of Mg-based alloys with high hydrogen storage density,Mg−RE−TM(RE=rare earth,TM=metallic element)alloys have been extensively researc...To address the challenges posed by high reaction temperatures and the slow kinetics of Mg-based alloys with high hydrogen storage density,Mg−RE−TM(RE=rare earth,TM=metallic element)alloys have been extensively researched and hold great promise.In this study,a series of Mg−RE−TM based Mg_(90)Y_(2)Ce_(2)Ni_(3)Al_(3-x)Sc_(x)(x=0,0.3,0.6,0.9,1.2)alloys were prepared.The addition of Sc element has been found to enhance the activation and kinetic properties of the alloy.Compared with the significant differences in the first four dehydrogenation curves of the Sc0 sample,the first activated dehydrogenation curve of the Sc1.2 alloy overlaps with the fully activated dehydrogenation curve.The dehydrogenation activation energy decreased from 96.56 kJ/mol in the Sc0 alloy to 63.69 kJ/mol in the Sc0.9 alloy.Through analysis of the microstructure,phase composition,and hydrogen absorption and desorption kinetics of the alloy,the mechanisms for improving the hydrogen storage properties of the alloy were elucidated.The nucleation-growth-impingement Avrami model was employed to accurately simulate the hydrogen storage kinetics.The results showed that stage II was prolonged and accelerated at high temperature,and the growth rate and hydrogen storage of stage I were increased at low temperature in hydrogen absorption.Microstructure analysis revealed the presence of Mg,CeMg_(12),Mg_(47)Y,and YNi_(2)Al_(3) phases in the Sc0 sample.Upon the addition of Sc element,a new phase,ScNiAl,was formed,and the coarse grain size of the main phase was significantly refined.This refinement provides faster diffusion channels for hydrogen atoms,accelerating the phase transition between Mg alloys and hydrides.The microstructure changes explain the improved activation properties,effective hydrogen absorption and desorption capacity,and kinetic properties of the Mg-based samples.展开更多
The crisis of excessive increase in CO_(2)emissions has quickly become a serious issue and requires low-cost and bio-compatible solutions.The employee of membrane technology for CO_(2)gas separation has garnered signi...The crisis of excessive increase in CO_(2)emissions has quickly become a serious issue and requires low-cost and bio-compatible solutions.The employee of membrane technology for CO_(2)gas separation has garnered significant interest among researchers.However,this method encounters challenges related to selectivity and permeability.Therefore,modifying and reinforcing the polymer membranes to improve gas separation performance seems essential.Among the various methods for polymer membrane modification,modification with magnesium-based fillers to prepare a mixed matrix membrane(MMM)is considered an efficient method.Owing to magnesium metal's low weight,low density,high strength,and good selectivity,magnesium-based materials(Mg-based materials)have more porosity,higher available surface area,more adsorption sites,lighter weight,and more gas absorption tendency than other fillers,which makes them an attractive choice for the preparation of gas separation MMMs.This research deals with the introduction of Mg-based materials,various methods of synthesis of Mg-based materials,different methods of introducing Mg-based materials into the membrane matrix,and their effect on the performance of MMMs in CO_(2)gas separation applications.Therefore,this review can provide researchers with light horizons in using the high potential of Mg-based materials as efficient fillers in MMMs to achieve excellent permeability and selectivity and generally improve their performance in CO_(2)gas separation applications.展开更多
The magnesium-based materials are acknowledged as one of the most promising solid-state hydrogen storage mediums,attributed to their superior hydrogen storage capacity.Nevertheless,challenges such as sluggish kinetics...The magnesium-based materials are acknowledged as one of the most promising solid-state hydrogen storage mediums,attributed to their superior hydrogen storage capacity.Nevertheless,challenges such as sluggish kinetics,thermodynamic stability,inadequate cycling stability,and difficulties in activation impede the commercial utilization of Mg-based composites.Research indicates that reducing material dimensions to the nanoscale represents an efficacious strategy to address these issues.In this work,we systematically analyze the impact of nanosizing on Mg-based composites from three perspectives:nano-substrate modulation,nano-catalyst construction,and nano-catalytic mechanism.This analysis aims to provide guidance for the optimization and development of nanosizing strategies.For the regulation of nanosizing of Mg-based composites,the nanosizing of multi-element micro-alloyed Mg-rich systems,the integrated synthesis of multi-element multi-component nano-catalysts,and the coexistence of multiple nano-catalytic mechanisms are proposed in the light of the current state of the art research,artificial intelligence technology,and advanced characterization technology to achieve efficient,multidimensional,and simultaneous regulation of the hydrogen storage performance of Mg-based composites.This paper also envisions future directions and potential applications,emphasizing the importance of interdisciplinary approaches that integrate material science,chemistry,and computational modeling to overcome existing limitations and unlock the full potential of Mg-based hydrogen storage technologies.展开更多
While early transition metal-based materials,such as MXene,has emerged as an efficient catalyst for the Mg-based hydrogen storage materials,their strong interaction with hydrogen resulted in the high hydrogen diffusio...While early transition metal-based materials,such as MXene,has emerged as an efficient catalyst for the Mg-based hydrogen storage materials,their strong interaction with hydrogen resulted in the high hydrogen diffusion barrier,hindering further improvement of catalytic activity.A MXene is characterized by rich anionic groups on its surface,significantly affecting electronic and catalytic functionalities.Using Nb_(2)CT_(x)as an example,we herein illustrate the critical role of anionic T_(x)defects on controlling hydrogen dissociation and diffusion processes in Mg-based hydrogen storage materials.The hydrogen desorption properties of MgH_(2)can be significantly enhanced by utilizing T_(x)controllable Nb_(2)CT_(x),and it can release 3.57 wt.%hydrogen within 10 min under 240℃with the reduced dehydrogenation activation barrier.It also realized stable de/hydrogenation reactions for at least 50 cycles.DFT studies combined with kinetic analysis revealed that the catalyst‒hydrogen interaction could be systematically controlled by optimizing surface T_(x)defect density,accelerating the hydrogen dissociation and diffusion processes at the same time.These results demonstrate that the T_(x)defects serve as the effective catalytically active centers of Nb_(2)CT_(x),offering a flexible catalyst design guideline.展开更多
Aqueous alkali metal-ion batteries(AAMIBs)have been recognized as emerging electrochemical energy storage technologies for grid-scale applications owning to their intrinsic safety,cost-effectiveness,and environmental ...Aqueous alkali metal-ion batteries(AAMIBs)have been recognized as emerging electrochemical energy storage technologies for grid-scale applications owning to their intrinsic safety,cost-effectiveness,and environmental sustainability.However,the practical application of AAMIBs is still severely constrained by the tendency of aqueous electrolytes to freeze at low temperatures and decompose at high temperatures,limiting their operational temperature range.Considering the urgent need for energy systems with higher adaptability and resilience at various application scenarios,designing novel electrolytes via structure modulation has increasingly emerged as a feasible and economical strategy for the performance optimization of wide-temperature AAMIBs.In this review,the latest advancement of wide-temperature electrolytes for AAMIBs is systematically and comprehensively summarized.Specifically,the key challenges,failure mechanisms,correlations between hydrogen bond behaviors and physicochemical properties,and thermodynamic and kinetic interpretations in aqueous electrolytes are discussed firstly.Additionally,we offer forward-looking insights and innovative design principles for developing aqueous electrolytes capable of operating across a broad temperature range.This review is expected to provide some guidance and reference for the rational design and regulation of widetemperature electrolytes for AAMIBs and promote their future development.展开更多
Mg and its alloys are drawing huge attention since the last two decades as a viable option for temporary implants applications.A commendable progress has already been made in the development of these alloys.The biodeg...Mg and its alloys are drawing huge attention since the last two decades as a viable option for temporary implants applications.A commendable progress has already been made in the development of these alloys.The biodegradable nature of Mg,appreciable biocompatibility of elemental Mg,and its close resemblance to natural bone in terms of density and elastic modulus make them highly preferable option amongst other available alternatives in this field.This review article presents an overview covering the recent advancements made in the field of Mg-based biodegradable implants for orthopaedic implant applications.The paper focuses on alloy development and fabrication techniques,the state of the art of important Mg-based alloy systems in terms of their mechanical properties,in-vitro and in-vivo degradation behaviour and cytotoxicity.Further,the paper reviews the current progress achieved in the clinical transition of Mg-based alloys for orthopaedic fixtures.The review also includes the degradation mechanisms of the alloys in physiological environment and highlights the mismatch existing between the rate of bone healing and alloy degradation due to rapid corrosion of the alloys in such environment,which has still restricted their widespread application.Finally,the surface coating techniques available for the alloys as an effective way to reduce the degradation rate are reviewed,followed by a discussion on the future research prospects.展开更多
With the depletion of fossil fuels and global warming,there is an urgent demand to seek green,low-cost,and high-efficiency energy resources.Hydrogen has been considered as a potential candidate to replace fossil fuels...With the depletion of fossil fuels and global warming,there is an urgent demand to seek green,low-cost,and high-efficiency energy resources.Hydrogen has been considered as a potential candidate to replace fossil fuels,due to its high gravimetric energy density(142 MJ kg^(-1)),high abundance(H_(2)O),and environmentalfriendliness.However,due to its low volume density,effective and safe hydrogen storage techniques are now becoming the bottleneck for the"hydrogen economy".Under such a circumstance,Mg-based hydrogen storage materials garnered tremendous interests due to their high hydrogen storage capacity(~7.6 wt%for MgH_(2)),low cost,and excellent reversibility.However,the high thermodynamic stability(ΔH=-74.7 kJ mol^(-1)H_(2))and sluggish kinetics result in a relatively high desorption temperature(>300℃),which severely restricts widespread applications of MgH_(2).Nano-structuring has been proven to be an effective strategy that can simultaneously enhance the ab/de-sorption thermodynamic and kinetic properties of MgH_(2),possibly meeting the demand for rapid hydrogen desorption,economic viability,and effective thermal management in practical applications.Herein,the fundamental theories,recent advances,and practical applications of the nanostructured Mg-based hydrogen storage materials are discussed.The synthetic strategies are classified into four categories:free-standing nano-sized Mg/MgH_(2)through electrochemical/vapor-transport/ultrasonic methods,nanostructured Mg-based composites via mechanical milling methods,construction of core-shell nano-structured Mg-based composites by chemical reduction approaches,and multi-dimensional nano-sized Mg-based heterostructure by nanoconfinement strategy.Through applying these strategies,near room temperature ab/de-sorption(<100℃)with considerable high capacity(>6 wt%)has been achieved in nano Mg/MgH_(2)systems.Some perspectives on the future research and development of nanostructured hydrogen storage materials are also provided.展开更多
Hydrogen energy is expected to be an“ideal fuel”in the era of decarbonization.The discovery,de-velopment,and modification of high-performance hydrogen storage materials are the keys to the fu-ture development of sol...Hydrogen energy is expected to be an“ideal fuel”in the era of decarbonization.The discovery,de-velopment,and modification of high-performance hydrogen storage materials are the keys to the fu-ture development of solid-state hydrogen storage and hydrogen energy utilization.Magnesium hydride(MgH_(2)),with its high hydrogen storage capacity,abundant natural reserves,and environmental friend-liness,has been extensively researched.Herein,we briefly summarize the typical structure and hy-drogenation/dehydrogenation reaction mechanism of MgH_(2)and provide a comprehensive overview of strategies to effectively tune the thermodynamics and kinetics of Mg-based materials,such as alloy-ing,nanosizing,the introduction of additives,and composite modification.With substantial efforts,great achievements have been achieved,such as lower absorption/desorption temperatures and better cy-cling stability.Nonetheless,some pivotal issues remain to be addressed,such as unfavorable hydro-genation/dehydrogenation factors,harsh conditions,slow kinetics,incomplete dehydrogenation,low hy-drogen purity,expensive catalysts,and a lack of valid exploration of mechanisms in the hydrogena-tion/dehydrogenation process.Lastly,some future development prospects of MgH_(2)in energy-efficient conversion and storage have been presented,including advanced manufacturing ways,stabilization of nanostructures,the introduction of additives combined with structural modification,and utilization of advanced characterization techniques.展开更多
Aiming to elucidate the hydrogen absorption/desorption cycling properties of Mg-based alloys with in-situ formed Mg_(2)Ni and LaH_(x)(x=2,3)nanocrystallines,the hydrogen storage cycle stability,hydriding/dehydriding c...Aiming to elucidate the hydrogen absorption/desorption cycling properties of Mg-based alloys with in-situ formed Mg_(2)Ni and LaH_(x)(x=2,3)nanocrystallines,the hydrogen storage cycle stability,hydriding/dehydriding cycling kinetics and thermodynamic stability of the experimental alloys have been investigated in detail.The results show that the Mg-Ni-La alloys exhibit improved hydrogen storage cycling properties and can remain storage hydrogen above 5.5 wt%after 200 cycles.With the increase of cycling numbers,the dehydrogenation rates of the experimental samples increase firstly and then gradually decrease,and eventually maintain relative stable state.Microstructure observation reveals that powders sintering and hydrogen decrepitation both exist during hydrogen absorption/desorption cycles due to repeated volume expansion and contraction.Meanwhile,the in-situ formed LaH_(x)(x=2,3)and Mg_(2)Ni nanocrystallines stabilize the microstructures of the particles and hinder the powders sintering.After 200 cycles,the average particle size of the experimental samples decreases and the specific surface area apparently increases,which leads to the decomposition temperatures of MgH_(2)and Mg_(2)NiH_(4)slightly shift to lower temperatures.Moreover,Mg_(2)Ni and LaH_(x)(x=2,3)have been proven to be stable catalysts during long-term cycling,which can still uniformly distribute within the powders after 200 cycles.展开更多
The effect of heat-treatment process on the properties of Mm0.8Mg0.2(NiCoAlMn)3.5 hydrogen storage alloy was discussed . The electrochemical properties such as cycling stability, activation property, and the plateau v...The effect of heat-treatment process on the properties of Mm0.8Mg0.2(NiCoAlMn)3.5 hydrogen storage alloy was discussed . The electrochemical properties such as cycling stability, activation property, and the plateau voltage of the alloy which was heat-treated in various temperatures and times had different changes during the cycle process, the optimum heat-treatment conditions of this alloy were determined by this work.展开更多
The composites comprised of Co nanoparticle and C nanosheet were prepared though a high-temperature carbonization reaction.The catalysis of Co@C composites on the hydrogen storage behavior of Mg_(90)Ce_(5)Y_(5)alloy w...The composites comprised of Co nanoparticle and C nanosheet were prepared though a high-temperature carbonization reaction.The catalysis of Co@C composites on the hydrogen storage behavior of Mg_(90)Ce_(5)Y_(5)alloy was investigated in detail by XRD,SEM,TEM,PCI,and DSC method.Because of the synergistic catalytic function of C and Co in C@Co nanocomposites,the Mg_(90)Ce_(5)Y_(5)alloy with 10 wt.%C@Co shows the excellent hydrogen absorption and desorption performances.Time for releasing hydrogen reduces from 150 min to 11 min with the addition of the C@Co composites at the temperature of 300℃.Meanwhile,the dehydrogenation activation energy also declines from 130.3 to 81.9 kJ mol^(-1)H_(2)after the addition of the C@Co composites.This positive effect attributes to the C layer with the high defect density and the Co nanoparticles,which reduces the energy barriers for the nucleation of Mg/MgH_(2)phase and the recombination of hydrogen molecule.Besides,the C@Co composites also improve the activation property of the Mg_(90)Ce_(5)Y_(5)alloy which was folly activated in the first cycle.Moreover,the temperature for initial dehydrogenation and the endothermic peak of the alloy hydride were also decreased.Although the addition of the C@Co composites increases the plateau pressures and decreases the value of the decomposition enthalpy,these differences are so small that the improvement on thermodynamics can hardly be seen.展开更多
The Al-based amorphous and nanocrystalline composite coatings with the composition of Al-Ni-Y-Co and Al-Ni-Mm-Fe were prepared on AZ91 Mg-based alloys by high velocity arc spraying technique(HVAS).The structure charac...The Al-based amorphous and nanocrystalline composite coatings with the composition of Al-Ni-Y-Co and Al-Ni-Mm-Fe were prepared on AZ91 Mg-based alloys by high velocity arc spraying technique(HVAS).The structure character of the coatings indicates that coatings contain the mixture of amorphous phases and crystalline and there are both less than 2%porosity.The electrochemical tests of the coatings and the substrate were studied.The coatings show the passivation ability during polarization,but AZ91 Mg-based alloys show little passivation.The corrosion current density of the coatings is lower than that of AZ91 Mg-based alloys.The results show that the coatings have an excellent corrosion resistance for AZ91 Mg-based alloys in 5 wt%NaCl solution.展开更多
A sort of rare earth Mg-based system hydrogen storage alloys with AB3-type was prepared by double-roller rapid quenching method. The alloys were nanocrystalline multi-phase structures composed of LaNi3 phase and LaNi5...A sort of rare earth Mg-based system hydrogen storage alloys with AB3-type was prepared by double-roller rapid quenching method. The alloys were nanocrystalline multi-phase structures composed of LaNi3 phase and LaNi5 phase by X-ray diffraction and scanning electron microscopy analyses, and the suitable absorption/desorption plateau was revealed by the measurement of P-C-I curve. Electrochemical studies indicate that the alloys exhibit good electrochemical properties such as high capacity and stable cycle life, and the discharge capacity is 369 mAh·g-1 at 0.2 C (72 mA·g-1). after 460 cycles, the capacity decay was only 19.4% at 2 C (720 mA·g-1).展开更多
Biodegradable magnesium(Mg) and its alloy show huge potential as temporary bone substitute due to the favorable biocompatibility and mechanical compatibility. However, one issue deserves attention is the too fast degr...Biodegradable magnesium(Mg) and its alloy show huge potential as temporary bone substitute due to the favorable biocompatibility and mechanical compatibility. However, one issue deserves attention is the too fast degradation. In this work, mesoporous bioglass(MBG)with high pore volume(0.59 cc/g) and huge specific surface area(110.78 m^(2)/g) was synthesized using improved sol-gel method, and introduced into Mg-based composite via laser additive manufacturing. Immersion tests showed that the incorporated MBG served as powerful adsorption sites, which promoted the in-situ deposition of apatite by successively adsorbing Ca2+and HPO42-. Such dense apatite film acted as an efficient protection layer and enhanced the corrosion resistance of Mg matrix, which was proved by the electrochemical impedance spectroscopy measurements. Thereby, Mg based composite showed a significantly decreased degradation rate of 0.31 mm/year. Furthermore,MBG also improved the mechanical properties as well as cell behavior. This work highlighted the advantages of MBG in the fabrication of Mg-based implant with enhanced overall performance for orthopedic application.展开更多
Both the solid solution and precipitation are mainly strengthening mechanism for the magnesium-based alloys. A great number of alloying elements can be dissolved into the Mg matrix to form the solutes and precipitates...Both the solid solution and precipitation are mainly strengthening mechanism for the magnesium-based alloys. A great number of alloying elements can be dissolved into the Mg matrix to form the solutes and precipitates.Moreover, the type of precipitates varies with different alloying elements and heat treatments, which makes it quite difficult to understand the formation mechanism of the precipitates in Mg-based alloys in depth. Thus, it is very hard to give a systematical regularity in precipitation process for the Mg-based alloys. This review is mainly focused on the formation and microstructural evolution of the precipitates, as a hot topic for the past few years, including Guinier-Preston Zones, quasicrystals and long-period stacking ordered phases formed in a number of Mg-TM-RE alloy systems, where TM = Al, Zn, Zr and RE = Y,Gd, Hd, Ce and La.展开更多
Mg-based hydrogen storage materials are considered to be one of the most promising solid-state hydrogen storage materials due to their large hydrogen storage capacity and low cost. However, slow hydrogen absorption/de...Mg-based hydrogen storage materials are considered to be one of the most promising solid-state hydrogen storage materials due to their large hydrogen storage capacity and low cost. However, slow hydrogen absorption/desorption rate and excessive hydrogen absorption/desorption temperature limit the application of Mg-based hydrogen storage materials.The present paper reviews the advances in the research of Mg-based hydrogen storage film in recent years, including the advantage of the film, the function theory of fabricating method and its functional theory, and the influencing factors in the technological process. The research status worldwide is introduced in detail. By comparing pure Mg, Pd-caped Mg, nonpalladium capped Mg, and Mg alloy hydrogen storage films, an ideal tendency for producing Mg-based film is pointed out,for example, looking for a cheap metal element to replace the high-priced Pd, compositing Mg film with other hydrogen storage alloy of catalytic elements, and so on.展开更多
Mg-based porous materials,as potential bone tissue engineering scaffolds,are considered an attractive strategy for bone repair owing to favorable biodegradability,good biocompatibility and suitable mechanical properti...Mg-based porous materials,as potential bone tissue engineering scaffolds,are considered an attractive strategy for bone repair owing to favorable biodegradability,good biocompatibility and suitable mechanical properties.In this work,3D-cubic interconnected porous Mg–xZn–0.3Ca(x=0,3,6)scaffolds were prepared to obtain desirable pore structures with a mean porosity up to 73%and main pore size of 400–500μm,which pore structures were close to the human cancellous bone.The structure–property relationships in the present scaffolds were analyzed by experiments and theoretical models of generalized method of cells(GMC).Mg–xZn–0.3Ca scaffolds exhibited good compression properties with a maximum above 5MPa in yield strength and about 0.4GPa in elastic modulus.This was attributed to not only the alloy strengthening but also the large minimum solid area.On the other hand,the scaffolds showed undesirable and relatively serious degradation behavior in Hank’s solution,resulting from Zn addition in Mg-based scaffolds and the high surface area ratio in the pore structure.Therefore,surface modifications are worth studying for controlled degradation in the future.In conclusion,this research would explore a novel attempt to introduce 3D-cubic pore structure for Mg-based scaffolds,and provide new insights into the preparations of Mg-based scaffolds with good service performances for bone repair.展开更多
As an example of the La-Mg-Y system, the method how to set up the themaodynamic model of individual phases was introduced in the process of thermodynamic optimization. The solution phases （liquid, body-centered cubic...As an example of the La-Mg-Y system, the method how to set up the themaodynamic model of individual phases was introduced in the process of thermodynamic optimization. The solution phases （liquid, body-centered cubic, face-centered cubic, hexagonal close-packed and double hexagonal close-packed） were modeled with the Redlich-Kister equation. The compound energy model has been used to describe the thermodynamic functions of the intermetallic compounds in the La-Mg-Y systems. The compounds Mg2Y, Mg24Y5, Mg12La, Mg17La2, Mg41Las, Mg3La and Mg2La in the La-Mg-Y system were treated as the formulae （Mg,Y）2（La,Mg,Y）, Mg24（La,Mg,Y）4Y, Mg12（La, Y）, Mg17（La,Y）2, Mg41（La,Y）5, Mg3（La,Mg,Y） and Mg2（La, Y）, respectively. A model （La, Mg,Y）0.5（La,Mg,Y）0.5 was applied to describe the compound MgM formed by MgLa and MgY in order to cope with the order-disorder transition between body-centered cubic solution （A2） and MgM with CsCl-type structure （B2） in the La-Mg-Y system. The Gibbs energies of individual phases were optimized in the La-Mg, La-Y and La-Mg-Y systems by CALPHAD technique. The projection of the liquidus surfaces for the La-Mg-Y system was predicted. The Mg-based alloys database including 36 binary and 15 ternary systems formed by Mg, Al, Cu, Ni, Mn, Zn and rare earth elements was set up in SGTE standard.展开更多
Thethermal stability and the kinetics of grain growth of nanocrystalline Mg-6Al-1Zn and Mg-6Al-1Zn-1Si alloys prepared via mechanical alloying were investigated. It started with elemental powders, using a variety of a...Thethermal stability and the kinetics of grain growth of nanocrystalline Mg-6Al-1Zn and Mg-6Al-1Zn-1Si alloys prepared via mechanical alloying were investigated. It started with elemental powders, using a variety of analytical techniques including differential scanning calorimetry （DSC）, X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM） and energy dispersive spectrometry. The kinetics of grain growth in isothermal annealing was investigated. The XRD results show that, although the grain sizes of both material systems increase as the annealing temperature rises, the Si-containing system displays a relatively smaller grain size, i.e., 60 nm compared with 72 nm in Mg-6Al-1Zn system, after being exposed to 350 ℃ for 1 h. The second-phase intermetallic particle Mg2Si formed during the isothermal annealing of Mg-6Al-1Zn-1Si system could influence not only the activation energy but also the exponent of kinetic equation. Higher hardness values obtained in the Si-containing system would be due to the formation of Mg2Si intermetallic phase.展开更多
基金financially supported by the Natural Science Foundation of China (31070528)Project of China “Twelfth Five-Year” National Science and Technology Supporting Plan (2011BAC11B04)the Foundation of State Key Laboratory of Pulp and Paper Engineering
文摘In this study,Mg O was partially used as an alkali source in the peroxide bleaching process of bleached chemi-thermomechanical pulp(BCTMP).The effects of substitution percentage of Mg O for Na OH on the bulk,optical,and physical properties of bleached pulp,and the main effluent characteristics were analyzed.In addition,the influencing mechanism of Mgbased alkali on the strength properties of the BCTMP was further investigated.Strength properties of the BCTMPs were investigated as a function of charge characteristics,fiber morphology,surface lignin content,relative bonding area,and hydrogen bonds of the BCTMP.The results showed that cationic demand(CD) and chemical oxygen demand(COD_(Cr)) of the bleaching effluent decreased as the substitution percentage of Mg O for Na OH increased; meanwhile,the bulk and optical properties of the BCTMP increased.Nevertheless,the strength properties(tensile,tear,and burst indices) of the bleached pulp decreased as the substitution percentage of Mg O for Na OH increased.The decrease in the fiber charge density and increase in the surface lignin content affected the fiber swelling,resulting in a decline in pulp interfibers bonding strength and further loss of the tensile and burst indices.
基金National Natural Science Foundation of China(51871125)the Major Programs of Central Iron and Steel Research Institute(No.23020230ZD)for financial support of the work.
文摘To address the challenges posed by high reaction temperatures and the slow kinetics of Mg-based alloys with high hydrogen storage density,Mg−RE−TM(RE=rare earth,TM=metallic element)alloys have been extensively researched and hold great promise.In this study,a series of Mg−RE−TM based Mg_(90)Y_(2)Ce_(2)Ni_(3)Al_(3-x)Sc_(x)(x=0,0.3,0.6,0.9,1.2)alloys were prepared.The addition of Sc element has been found to enhance the activation and kinetic properties of the alloy.Compared with the significant differences in the first four dehydrogenation curves of the Sc0 sample,the first activated dehydrogenation curve of the Sc1.2 alloy overlaps with the fully activated dehydrogenation curve.The dehydrogenation activation energy decreased from 96.56 kJ/mol in the Sc0 alloy to 63.69 kJ/mol in the Sc0.9 alloy.Through analysis of the microstructure,phase composition,and hydrogen absorption and desorption kinetics of the alloy,the mechanisms for improving the hydrogen storage properties of the alloy were elucidated.The nucleation-growth-impingement Avrami model was employed to accurately simulate the hydrogen storage kinetics.The results showed that stage II was prolonged and accelerated at high temperature,and the growth rate and hydrogen storage of stage I were increased at low temperature in hydrogen absorption.Microstructure analysis revealed the presence of Mg,CeMg_(12),Mg_(47)Y,and YNi_(2)Al_(3) phases in the Sc0 sample.Upon the addition of Sc element,a new phase,ScNiAl,was formed,and the coarse grain size of the main phase was significantly refined.This refinement provides faster diffusion channels for hydrogen atoms,accelerating the phase transition between Mg alloys and hydrides.The microstructure changes explain the improved activation properties,effective hydrogen absorption and desorption capacity,and kinetic properties of the Mg-based samples.
文摘The crisis of excessive increase in CO_(2)emissions has quickly become a serious issue and requires low-cost and bio-compatible solutions.The employee of membrane technology for CO_(2)gas separation has garnered significant interest among researchers.However,this method encounters challenges related to selectivity and permeability.Therefore,modifying and reinforcing the polymer membranes to improve gas separation performance seems essential.Among the various methods for polymer membrane modification,modification with magnesium-based fillers to prepare a mixed matrix membrane(MMM)is considered an efficient method.Owing to magnesium metal's low weight,low density,high strength,and good selectivity,magnesium-based materials(Mg-based materials)have more porosity,higher available surface area,more adsorption sites,lighter weight,and more gas absorption tendency than other fillers,which makes them an attractive choice for the preparation of gas separation MMMs.This research deals with the introduction of Mg-based materials,various methods of synthesis of Mg-based materials,different methods of introducing Mg-based materials into the membrane matrix,and their effect on the performance of MMMs in CO_(2)gas separation applications.Therefore,this review can provide researchers with light horizons in using the high potential of Mg-based materials as efficient fillers in MMMs to achieve excellent permeability and selectivity and generally improve their performance in CO_(2)gas separation applications.
基金financially supported by the Key Research and Development Projects of Shaanxi Province(Grant Nos.2025CYYBXM-154 and 2024GX-YBXM-213)the Yulin Science and Technology Bureau(Grant Nos.2023-CXY-202 and 2024-CXY-154)the Technology Innovation Leading Program of Shaanxi(Programs 2023GXLH-068)。
文摘The magnesium-based materials are acknowledged as one of the most promising solid-state hydrogen storage mediums,attributed to their superior hydrogen storage capacity.Nevertheless,challenges such as sluggish kinetics,thermodynamic stability,inadequate cycling stability,and difficulties in activation impede the commercial utilization of Mg-based composites.Research indicates that reducing material dimensions to the nanoscale represents an efficacious strategy to address these issues.In this work,we systematically analyze the impact of nanosizing on Mg-based composites from three perspectives:nano-substrate modulation,nano-catalyst construction,and nano-catalytic mechanism.This analysis aims to provide guidance for the optimization and development of nanosizing strategies.For the regulation of nanosizing of Mg-based composites,the nanosizing of multi-element micro-alloyed Mg-rich systems,the integrated synthesis of multi-element multi-component nano-catalysts,and the coexistence of multiple nano-catalytic mechanisms are proposed in the light of the current state of the art research,artificial intelligence technology,and advanced characterization technology to achieve efficient,multidimensional,and simultaneous regulation of the hydrogen storage performance of Mg-based composites.This paper also envisions future directions and potential applications,emphasizing the importance of interdisciplinary approaches that integrate material science,chemistry,and computational modeling to overcome existing limitations and unlock the full potential of Mg-based hydrogen storage technologies.
基金supported by Liuchuang Program of Chongqing Municipality(cx2022038)the Fundamental Research Funds for the Central Universities(2022CDJQY-013)the Graduate Research and Innovation Foundation of Chongqing,China(CYB22005).
文摘While early transition metal-based materials,such as MXene,has emerged as an efficient catalyst for the Mg-based hydrogen storage materials,their strong interaction with hydrogen resulted in the high hydrogen diffusion barrier,hindering further improvement of catalytic activity.A MXene is characterized by rich anionic groups on its surface,significantly affecting electronic and catalytic functionalities.Using Nb_(2)CT_(x)as an example,we herein illustrate the critical role of anionic T_(x)defects on controlling hydrogen dissociation and diffusion processes in Mg-based hydrogen storage materials.The hydrogen desorption properties of MgH_(2)can be significantly enhanced by utilizing T_(x)controllable Nb_(2)CT_(x),and it can release 3.57 wt.%hydrogen within 10 min under 240℃with the reduced dehydrogenation activation barrier.It also realized stable de/hydrogenation reactions for at least 50 cycles.DFT studies combined with kinetic analysis revealed that the catalyst‒hydrogen interaction could be systematically controlled by optimizing surface T_(x)defect density,accelerating the hydrogen dissociation and diffusion processes at the same time.These results demonstrate that the T_(x)defects serve as the effective catalytically active centers of Nb_(2)CT_(x),offering a flexible catalyst design guideline.
基金supported by the National Natural Science Foundation of China(52002297)National Key R&D Program of China(2022VFB2404800)+1 种基金Wuhan Yellow Crane Talents Program,China Postdoctoral Science Foundation(No.2024M752495)the Postdoctoral Fellowship Program of CPSF(No.GZB20230552).
文摘Aqueous alkali metal-ion batteries(AAMIBs)have been recognized as emerging electrochemical energy storage technologies for grid-scale applications owning to their intrinsic safety,cost-effectiveness,and environmental sustainability.However,the practical application of AAMIBs is still severely constrained by the tendency of aqueous electrolytes to freeze at low temperatures and decompose at high temperatures,limiting their operational temperature range.Considering the urgent need for energy systems with higher adaptability and resilience at various application scenarios,designing novel electrolytes via structure modulation has increasingly emerged as a feasible and economical strategy for the performance optimization of wide-temperature AAMIBs.In this review,the latest advancement of wide-temperature electrolytes for AAMIBs is systematically and comprehensively summarized.Specifically,the key challenges,failure mechanisms,correlations between hydrogen bond behaviors and physicochemical properties,and thermodynamic and kinetic interpretations in aqueous electrolytes are discussed firstly.Additionally,we offer forward-looking insights and innovative design principles for developing aqueous electrolytes capable of operating across a broad temperature range.This review is expected to provide some guidance and reference for the rational design and regulation of widetemperature electrolytes for AAMIBs and promote their future development.
文摘Mg and its alloys are drawing huge attention since the last two decades as a viable option for temporary implants applications.A commendable progress has already been made in the development of these alloys.The biodegradable nature of Mg,appreciable biocompatibility of elemental Mg,and its close resemblance to natural bone in terms of density and elastic modulus make them highly preferable option amongst other available alternatives in this field.This review article presents an overview covering the recent advancements made in the field of Mg-based biodegradable implants for orthopaedic implant applications.The paper focuses on alloy development and fabrication techniques,the state of the art of important Mg-based alloy systems in terms of their mechanical properties,in-vitro and in-vivo degradation behaviour and cytotoxicity.Further,the paper reviews the current progress achieved in the clinical transition of Mg-based alloys for orthopaedic fixtures.The review also includes the degradation mechanisms of the alloys in physiological environment and highlights the mismatch existing between the rate of bone healing and alloy degradation due to rapid corrosion of the alloys in such environment,which has still restricted their widespread application.Finally,the surface coating techniques available for the alloys as an effective way to reduce the degradation rate are reviewed,followed by a discussion on the future research prospects.
基金support from the National Key Research&Development Program(2022YFB3803700)of ChinaNational Natural Science Foundation(No.52171186)financial support from the Center of Hydrogen Science,Shanghai Jiao Tong University。
文摘With the depletion of fossil fuels and global warming,there is an urgent demand to seek green,low-cost,and high-efficiency energy resources.Hydrogen has been considered as a potential candidate to replace fossil fuels,due to its high gravimetric energy density(142 MJ kg^(-1)),high abundance(H_(2)O),and environmentalfriendliness.However,due to its low volume density,effective and safe hydrogen storage techniques are now becoming the bottleneck for the"hydrogen economy".Under such a circumstance,Mg-based hydrogen storage materials garnered tremendous interests due to their high hydrogen storage capacity(~7.6 wt%for MgH_(2)),low cost,and excellent reversibility.However,the high thermodynamic stability(ΔH=-74.7 kJ mol^(-1)H_(2))and sluggish kinetics result in a relatively high desorption temperature(>300℃),which severely restricts widespread applications of MgH_(2).Nano-structuring has been proven to be an effective strategy that can simultaneously enhance the ab/de-sorption thermodynamic and kinetic properties of MgH_(2),possibly meeting the demand for rapid hydrogen desorption,economic viability,and effective thermal management in practical applications.Herein,the fundamental theories,recent advances,and practical applications of the nanostructured Mg-based hydrogen storage materials are discussed.The synthetic strategies are classified into four categories:free-standing nano-sized Mg/MgH_(2)through electrochemical/vapor-transport/ultrasonic methods,nanostructured Mg-based composites via mechanical milling methods,construction of core-shell nano-structured Mg-based composites by chemical reduction approaches,and multi-dimensional nano-sized Mg-based heterostructure by nanoconfinement strategy.Through applying these strategies,near room temperature ab/de-sorption(<100℃)with considerable high capacity(>6 wt%)has been achieved in nano Mg/MgH_(2)systems.Some perspectives on the future research and development of nanostructured hydrogen storage materials are also provided.
基金supported by the National Natu-ral Science Foundation of China(Nos.U20A20237,51863005,52271205,51871065,51971068,and 52101245)the Scientific Research and Technology Development Program of Guangxi(Nos.AA19182014,AD17195073,AA17202030-1,AB21220027,and 2021AB17045)+2 种基金National Natural Science Foundation of Guangxi Province(Nos.2021GXNSFBA075057,2018GXNSFDA281051,2014GXNSFAA118401,and 2013GXNSFBA019244)the Scientific Research and Technology Development Program of Guilin(Nos.20210102-4 and 20210216-1)Guangxi Bagui Scholar Founda-tion,Guilin Lijiang Scholar Foundation,Guangxi Collaborative Innovation centre of Structure and Property for New Energy and Materials,Guangxi Advanced Functional Materials Foundation and Application Talents Small Highlands,Chinesisch-Deutsche Kooperationsgruppe(No.GZ1528).
文摘Hydrogen energy is expected to be an“ideal fuel”in the era of decarbonization.The discovery,de-velopment,and modification of high-performance hydrogen storage materials are the keys to the fu-ture development of solid-state hydrogen storage and hydrogen energy utilization.Magnesium hydride(MgH_(2)),with its high hydrogen storage capacity,abundant natural reserves,and environmental friend-liness,has been extensively researched.Herein,we briefly summarize the typical structure and hy-drogenation/dehydrogenation reaction mechanism of MgH_(2)and provide a comprehensive overview of strategies to effectively tune the thermodynamics and kinetics of Mg-based materials,such as alloy-ing,nanosizing,the introduction of additives,and composite modification.With substantial efforts,great achievements have been achieved,such as lower absorption/desorption temperatures and better cy-cling stability.Nonetheless,some pivotal issues remain to be addressed,such as unfavorable hydro-genation/dehydrogenation factors,harsh conditions,slow kinetics,incomplete dehydrogenation,low hy-drogen purity,expensive catalysts,and a lack of valid exploration of mechanisms in the hydrogena-tion/dehydrogenation process.Lastly,some future development prospects of MgH_(2)in energy-efficient conversion and storage have been presented,including advanced manufacturing ways,stabilization of nanostructures,the introduction of additives combined with structural modification,and utilization of advanced characterization techniques.
基金supported by Natural Science Foundation of Shaanxi Province,China(2017JM5079)The 111 project(No.B08040)is also acknowledged.
文摘Aiming to elucidate the hydrogen absorption/desorption cycling properties of Mg-based alloys with in-situ formed Mg_(2)Ni and LaH_(x)(x=2,3)nanocrystallines,the hydrogen storage cycle stability,hydriding/dehydriding cycling kinetics and thermodynamic stability of the experimental alloys have been investigated in detail.The results show that the Mg-Ni-La alloys exhibit improved hydrogen storage cycling properties and can remain storage hydrogen above 5.5 wt%after 200 cycles.With the increase of cycling numbers,the dehydrogenation rates of the experimental samples increase firstly and then gradually decrease,and eventually maintain relative stable state.Microstructure observation reveals that powders sintering and hydrogen decrepitation both exist during hydrogen absorption/desorption cycles due to repeated volume expansion and contraction.Meanwhile,the in-situ formed LaH_(x)(x=2,3)and Mg_(2)Ni nanocrystallines stabilize the microstructures of the particles and hinder the powders sintering.After 200 cycles,the average particle size of the experimental samples decreases and the specific surface area apparently increases,which leads to the decomposition temperatures of MgH_(2)and Mg_(2)NiH_(4)slightly shift to lower temperatures.Moreover,Mg_(2)Ni and LaH_(x)(x=2,3)have been proven to be stable catalysts during long-term cycling,which can still uniformly distribute within the powders after 200 cycles.
文摘The effect of heat-treatment process on the properties of Mm0.8Mg0.2(NiCoAlMn)3.5 hydrogen storage alloy was discussed . The electrochemical properties such as cycling stability, activation property, and the plateau voltage of the alloy which was heat-treated in various temperatures and times had different changes during the cycle process, the optimum heat-treatment conditions of this alloy were determined by this work.
基金financially supported by the National Natural Science Foundations of China(51761032 and 51871125)the Natural Science Foundations of Inner Mongolia,China(No.2019BS05005)the Scientific Research Staring Foundation of Taiyuan University of Science and Technology(20202040)
文摘The composites comprised of Co nanoparticle and C nanosheet were prepared though a high-temperature carbonization reaction.The catalysis of Co@C composites on the hydrogen storage behavior of Mg_(90)Ce_(5)Y_(5)alloy was investigated in detail by XRD,SEM,TEM,PCI,and DSC method.Because of the synergistic catalytic function of C and Co in C@Co nanocomposites,the Mg_(90)Ce_(5)Y_(5)alloy with 10 wt.%C@Co shows the excellent hydrogen absorption and desorption performances.Time for releasing hydrogen reduces from 150 min to 11 min with the addition of the C@Co composites at the temperature of 300℃.Meanwhile,the dehydrogenation activation energy also declines from 130.3 to 81.9 kJ mol^(-1)H_(2)after the addition of the C@Co composites.This positive effect attributes to the C layer with the high defect density and the Co nanoparticles,which reduces the energy barriers for the nucleation of Mg/MgH_(2)phase and the recombination of hydrogen molecule.Besides,the C@Co composites also improve the activation property of the Mg_(90)Ce_(5)Y_(5)alloy which was folly activated in the first cycle.Moreover,the temperature for initial dehydrogenation and the endothermic peak of the alloy hydride were also decreased.Although the addition of the C@Co composites increases the plateau pressures and decreases the value of the decomposition enthalpy,these differences are so small that the improvement on thermodynamics can hardly be seen.
基金National Natural Science Foundation of China(50905185)National"863"project of China(2009AA03Z342)
文摘The Al-based amorphous and nanocrystalline composite coatings with the composition of Al-Ni-Y-Co and Al-Ni-Mm-Fe were prepared on AZ91 Mg-based alloys by high velocity arc spraying technique(HVAS).The structure character of the coatings indicates that coatings contain the mixture of amorphous phases and crystalline and there are both less than 2%porosity.The electrochemical tests of the coatings and the substrate were studied.The coatings show the passivation ability during polarization,but AZ91 Mg-based alloys show little passivation.The corrosion current density of the coatings is lower than that of AZ91 Mg-based alloys.The results show that the coatings have an excellent corrosion resistance for AZ91 Mg-based alloys in 5 wt%NaCl solution.
文摘A sort of rare earth Mg-based system hydrogen storage alloys with AB3-type was prepared by double-roller rapid quenching method. The alloys were nanocrystalline multi-phase structures composed of LaNi3 phase and LaNi5 phase by X-ray diffraction and scanning electron microscopy analyses, and the suitable absorption/desorption plateau was revealed by the measurement of P-C-I curve. Electrochemical studies indicate that the alloys exhibit good electrochemical properties such as high capacity and stable cycle life, and the discharge capacity is 369 mAh·g-1 at 0.2 C (72 mA·g-1). after 460 cycles, the capacity decay was only 19.4% at 2 C (720 mA·g-1).
基金National Natural Science Foundation of China (51935014,52165043, 82072084, 81871498)Jiang Xi Provincial Natural Science Foundation of China (20192ACB20005,2020ACB214004)+6 种基金The Provincial Key R&D Projects of Jiangxi (20201BBE51012)Guangdong Province Higher Vocational Colleges&Schools Pearl River Scholar Funded Scheme (2018)Shenzhen Science and Technology Plan Project (JCYJ20170817112445033)Innovation Team Project on University of Guangdong Province(2018GKCXTD001)Technology Innovation Platform Project of Shenzhen Institute of Information Technology 2020(PT2020E002)China Postdoctoral Science Foundation(2020M682114)Open Research Fund of Jiangsu Key Laboratory of Precision and Micro-Manufacturing Technology。
文摘Biodegradable magnesium(Mg) and its alloy show huge potential as temporary bone substitute due to the favorable biocompatibility and mechanical compatibility. However, one issue deserves attention is the too fast degradation. In this work, mesoporous bioglass(MBG)with high pore volume(0.59 cc/g) and huge specific surface area(110.78 m^(2)/g) was synthesized using improved sol-gel method, and introduced into Mg-based composite via laser additive manufacturing. Immersion tests showed that the incorporated MBG served as powerful adsorption sites, which promoted the in-situ deposition of apatite by successively adsorbing Ca2+and HPO42-. Such dense apatite film acted as an efficient protection layer and enhanced the corrosion resistance of Mg matrix, which was proved by the electrochemical impedance spectroscopy measurements. Thereby, Mg based composite showed a significantly decreased degradation rate of 0.31 mm/year. Furthermore,MBG also improved the mechanical properties as well as cell behavior. This work highlighted the advantages of MBG in the fabrication of Mg-based implant with enhanced overall performance for orthopedic application.
基金supported by National Natural Science Fundation of China (Nos. 51171192 and51271183)National Basic Research Program of China(No. 2013CB632205)Innovation Fund of Institute of Metal Research (IMR), Chinese Academy of Sciences(CAS)
文摘Both the solid solution and precipitation are mainly strengthening mechanism for the magnesium-based alloys. A great number of alloying elements can be dissolved into the Mg matrix to form the solutes and precipitates.Moreover, the type of precipitates varies with different alloying elements and heat treatments, which makes it quite difficult to understand the formation mechanism of the precipitates in Mg-based alloys in depth. Thus, it is very hard to give a systematical regularity in precipitation process for the Mg-based alloys. This review is mainly focused on the formation and microstructural evolution of the precipitates, as a hot topic for the past few years, including Guinier-Preston Zones, quasicrystals and long-period stacking ordered phases formed in a number of Mg-TM-RE alloy systems, where TM = Al, Zn, Zr and RE = Y,Gd, Hd, Ce and La.
基金Project supported by the Competitiveness Enhancement Program of National Research Tomsk Polytechnic University(Grant No.VIU-OEF-66/2019)
文摘Mg-based hydrogen storage materials are considered to be one of the most promising solid-state hydrogen storage materials due to their large hydrogen storage capacity and low cost. However, slow hydrogen absorption/desorption rate and excessive hydrogen absorption/desorption temperature limit the application of Mg-based hydrogen storage materials.The present paper reviews the advances in the research of Mg-based hydrogen storage film in recent years, including the advantage of the film, the function theory of fabricating method and its functional theory, and the influencing factors in the technological process. The research status worldwide is introduced in detail. By comparing pure Mg, Pd-caped Mg, nonpalladium capped Mg, and Mg alloy hydrogen storage films, an ideal tendency for producing Mg-based film is pointed out,for example, looking for a cheap metal element to replace the high-priced Pd, compositing Mg film with other hydrogen storage alloy of catalytic elements, and so on.
基金This work was supported by the National Key Research and Development Program of China(No.2016YFC1102402)the National Natural Science Foundation of China(No.51771054,No.51971062)+1 种基金the Science and Technology Project of Jiangsu Province(No.BE2019679)the Fundamental Research Funds for the Central Universities(No.2242018K3DN03,No.2242019K40057).
文摘Mg-based porous materials,as potential bone tissue engineering scaffolds,are considered an attractive strategy for bone repair owing to favorable biodegradability,good biocompatibility and suitable mechanical properties.In this work,3D-cubic interconnected porous Mg–xZn–0.3Ca(x=0,3,6)scaffolds were prepared to obtain desirable pore structures with a mean porosity up to 73%and main pore size of 400–500μm,which pore structures were close to the human cancellous bone.The structure–property relationships in the present scaffolds were analyzed by experiments and theoretical models of generalized method of cells(GMC).Mg–xZn–0.3Ca scaffolds exhibited good compression properties with a maximum above 5MPa in yield strength and about 0.4GPa in elastic modulus.This was attributed to not only the alloy strengthening but also the large minimum solid area.On the other hand,the scaffolds showed undesirable and relatively serious degradation behavior in Hank’s solution,resulting from Zn addition in Mg-based scaffolds and the high surface area ratio in the pore structure.Therefore,surface modifications are worth studying for controlled degradation in the future.In conclusion,this research would explore a novel attempt to introduce 3D-cubic pore structure for Mg-based scaffolds,and provide new insights into the preparations of Mg-based scaffolds with good service performances for bone repair.
基金This work was financially supported by the National Natural Science Foundation of China (Nos. 50471095 and 50271008).
文摘As an example of the La-Mg-Y system, the method how to set up the themaodynamic model of individual phases was introduced in the process of thermodynamic optimization. The solution phases （liquid, body-centered cubic, face-centered cubic, hexagonal close-packed and double hexagonal close-packed） were modeled with the Redlich-Kister equation. The compound energy model has been used to describe the thermodynamic functions of the intermetallic compounds in the La-Mg-Y systems. The compounds Mg2Y, Mg24Y5, Mg12La, Mg17La2, Mg41Las, Mg3La and Mg2La in the La-Mg-Y system were treated as the formulae （Mg,Y）2（La,Mg,Y）, Mg24（La,Mg,Y）4Y, Mg12（La, Y）, Mg17（La,Y）2, Mg41（La,Y）5, Mg3（La,Mg,Y） and Mg2（La, Y）, respectively. A model （La, Mg,Y）0.5（La,Mg,Y）0.5 was applied to describe the compound MgM formed by MgLa and MgY in order to cope with the order-disorder transition between body-centered cubic solution （A2） and MgM with CsCl-type structure （B2） in the La-Mg-Y system. The Gibbs energies of individual phases were optimized in the La-Mg, La-Y and La-Mg-Y systems by CALPHAD technique. The projection of the liquidus surfaces for the La-Mg-Y system was predicted. The Mg-based alloys database including 36 binary and 15 ternary systems formed by Mg, Al, Cu, Ni, Mn, Zn and rare earth elements was set up in SGTE standard.
文摘Thethermal stability and the kinetics of grain growth of nanocrystalline Mg-6Al-1Zn and Mg-6Al-1Zn-1Si alloys prepared via mechanical alloying were investigated. It started with elemental powders, using a variety of analytical techniques including differential scanning calorimetry （DSC）, X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM） and energy dispersive spectrometry. The kinetics of grain growth in isothermal annealing was investigated. The XRD results show that, although the grain sizes of both material systems increase as the annealing temperature rises, the Si-containing system displays a relatively smaller grain size, i.e., 60 nm compared with 72 nm in Mg-6Al-1Zn system, after being exposed to 350 ℃ for 1 h. The second-phase intermetallic particle Mg2Si formed during the isothermal annealing of Mg-6Al-1Zn-1Si system could influence not only the activation energy but also the exponent of kinetic equation. Higher hardness values obtained in the Si-containing system would be due to the formation of Mg2Si intermetallic phase.
