Alkali metal thermochemical ablation is a promising anti-tumor therapy in which tumor tissue can be efficiently destroyed via both heat and hydroxyl ions released from the chemical reaction in tissue between an alkali...Alkali metal thermochemical ablation is a promising anti-tumor therapy in which tumor tissue can be efficiently destroyed via both heat and hydroxyl ions released from the chemical reaction in tissue between an alkali metal and water. Encouraging results have been reported from in vitro and in vivo trials in a previous study. However, the precise process of heat and mass transfer triggered by the above thermochemical reaction in tumor tissue has still remained confusing. Here, to better understand the temperature and p H responses of tumor tissue subject to alkali metal therapy, a theoretical model coupling temperature and concentration field is developed for characterizing the physicochemical reaction and the transport process occurring around the inserted sodium capsule during treatment. Preliminary experiments in tumor tissue are performed to validate the theoretical predictions of temperature, and the results indicate that the bioheat transfer model can predict the temperature responses in the tissues heated by the sodium capsule very well. Furthermore, comprehensive parametric studies are performed to evaluate the effects of either physiological or physicochemical parameters, including ablation time, time lags, and blood perfusion rate. Based on the numerical results, useful instructions are suggested for planning alkali metal tumor ablation treatment.展开更多
Alkali-free SiO_(2)-Al_(2)O_(3)-CaO-MgO with different SiO_(2)/Al_(2)O_(3)mass ratios was prepared by conventional melt quenching method.The glass network structure,thermodynamic properties and elastic modulus changes...Alkali-free SiO_(2)-Al_(2)O_(3)-CaO-MgO with different SiO_(2)/Al_(2)O_(3)mass ratios was prepared by conventional melt quenching method.The glass network structure,thermodynamic properties and elastic modulus changes with SiO_(2)and Al_(2)O_(3)ratios were investigated using various techniques.It is found that when SiO_(2)is replaced by Al_(2)O_(3),the Q^(4) to Q^(3) transition of silicon-oxygen network decreases while the aluminum-oxygen network increases,which result in the transformation of Si-O-Si bonds to Si-O-Al bonds and an increase in glass network connectivity even though the intermolecular bond strength decreases.The glass transition temperature(T_(g))increases continuously,while the thermal expansion coefficient increases and high-temperature viscosity first decreases and then increases.Meanwhile,the elastic modulus values increase from 93 to 102 GPa.This indicates that the elastic modulus is mainly affected by packing factor and dissociation energy,and elements with higher packing factors and dissociation energies supplant those with lower values,resulting in increased rigidity within the glass.展开更多
In order to realize the comprehensive utilization of industrial solid waste rice husk ash and heavy metal cadmium contaminated soil,rice husk ash-based geopolymer prepared by alkaline activator was used to modify cadm...In order to realize the comprehensive utilization of industrial solid waste rice husk ash and heavy metal cadmium contaminated soil,rice husk ash-based geopolymer prepared by alkaline activator was used to modify cadmium contaminated soil.The main physical and chemical properties of rice husk ash were clarified by SEM,XRF and X-ray diffraction.The unconfined compressive strength test and toxicity leaching test were carried out on the modified soil.Combined with FTIR and TG micro-level,the solidification mechanism of rice husk ash-based geopolymer solidified cadmium contaminated soil was discussed.The results show that the strength of geopolymer modified soil is significantly higher than that of plain soil,and the unconfined compressive strength at 7 d age is 4.2 times that of plain soil.The strength of modified soil with different dosage of geopolymer at 28 d age is about 36% to 40% higher than that of modified soil at 7 d age.Geopolymer has a significant effect on the leaching of heavy metals in contaminated soil.When the cadmium content is 100 mg/kg,it meets the standard limit.In the process of complex depolymerization-condensation reaction,on the one hand,geopolymers are cemented and agglomerated to form a complex spatial structure,which affects the macro and micro characteristics of soil.On the other hand,it has significant adsorption,precipitation and replacement effects on heavy metal ions in soil,showing good strength and low heavy metal leaching toxicity.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
Rechargeable alkali metal-sulfur(M-S)batteries,including Li/Na/K-S chemistries,have the potential to utilize abundant and low-cost sulfur cathodes yet offer high theoretical energy densities.However,their practical el...Rechargeable alkali metal-sulfur(M-S)batteries,including Li/Na/K-S chemistries,have the potential to utilize abundant and low-cost sulfur cathodes yet offer high theoretical energy densities.However,their practical electrochemical performance is fundamentally limited by the polysulfide shuttle effect.This challenge is particularly exacerbated in Na-S and K-S systems owing to larger metal-ion radii,weaker solvation energies,slower redox kinetics,and greater electrolyte-electrode incompatibilities compared to Li-S batteries.This review presents a comparative analysis of interface engineering strategies designed to suppress the shuttle effect across these three systems.Following a summary of sulfur cathode properties and reaction mechanisms,we systematically examine the origins of polysulfide shuttling.Our analysis progresses from functional separator design and interlayer enhancements to the implementation of solid-state electrolytes for root-cause inhibition.By evaluating interface engineering research specific to Na-S and K-S batteries,we elucidate both shared principles and unique challenges inherent to alkali M-S systems.Finally,we propose multifaceted solutions to achieve shuttlefree operation and enhance overall battery performance,thereby establishing a foundation for future advancements.展开更多
The hydrogen evolution reaction(HER)is crucial for hydrogen production and sustainable energy storage.Molybdenum disulfide(MoS_(2)),a representative transition metal dichalcogenides(TMDs),shows potential as an HER cat...The hydrogen evolution reaction(HER)is crucial for hydrogen production and sustainable energy storage.Molybdenum disulfide(MoS_(2)),a representative transition metal dichalcogenides(TMDs),shows potential as an HER catalyst but suffers from limited performance due to poor charge transfer and interfacial effects.Here,we report a salt-assisted chemical vapor deposition(CVD)method for synthesizing high-quality tungsten ditelluride(WTe_(2))with tunable morphologies using alkali halides(NaCl,KCl and LiCl).The prepared WTe_(2) nanoribbons and hexagonal nanosheets exhibit morphology-dependent electrical conductivity,with nanosheets showing superior performance.To evaluate WTe_(2) as a contact electrode,WTe_(2)−MoS_(2) heterostructures were fabricated and compared with graphene-MoS_(2) counterparts.The WTe_(2)−MoS_(2) heterostructure exhibits a superior Tafel slope of 111.57 mV/dec and an overpotential of 298 mV at-10 mA/cm^(2),significantly outperforming graphene-based electrodes.This improvement is attributed to the excellent conductivity of WTe_(2) and reduced interfacial Schottky barriers.Moreover,we systematically investigate the influence of WTe_(2) thickness on HER performance and assess the electrochemical durability and structural stability of the heterostructure,further confirming the effectiveness of WTe_(2) as a contact electrode for enhancing the HER activity of MoS_(2).This study offers a novel approach for enhancing the HER performance of MoS_(2) through controlled WTe_(2) growth and application as a contact electrode.Our findings provide valuable insights into the synthesis of high-quality WTe_(2) and broaden the potential applications of two-dimensional materials in energy catalysis.展开更多
We report a theoretical investigation into superconductivity within the MAXH_(6) quaternary hydride system using first-principles calculations,where M and A denote alkali and alkaline earth elements,respectively,and X...We report a theoretical investigation into superconductivity within the MAXH_(6) quaternary hydride system using first-principles calculations,where M and A denote alkali and alkaline earth elements,respectively,and X represents transition metal elements.Systematic analysis of electronic band structures,phonon dispersions,and electron-phonon coupling reveals that substitution of MA binary metal combinations and X metal atoms can create favorable conditions for superconductivity.Mapping of superconducting critical temperatures,combined with dynamical stability analysis through phonon calculations,identifies ten superconducting candidates at ambient pressure.Among these,LiNaAgH_(6) exhibits nearly-free-electron behavior reminiscent of monovalent electron superconductors.It demonstrates exceptional superconducting properties with electron–phonon coupling λ=2.707,which yields a superconducting transition temperature T_(c) of 206.4 K using the Allen–Dynes formula.Its structural analogs MgNaPdH_(6),LiMgPdH_(6),LiMgAgH_(6),LiMgAuH_(6) all exhibit superconducting transition temperatures above 110 K.These findings advance our fundamental understanding of superconductivity in quaternary hydrides and provide guidance for rational design of new high-temperature superconducting materials.展开更多
Using cemented rockfill to replace coal pillars offers an effective solution for reducing solid waste while ensuring the safety of gob-side entries.However,achieving the balance among low cost,high waste recycling rat...Using cemented rockfill to replace coal pillars offers an effective solution for reducing solid waste while ensuring the safety of gob-side entries.However,achieving the balance among low cost,high waste recycling rates,and adequate strength remains a significant challenge for cemented rockfill.This study used a composite alkali activator to activate gangue cemented rockfill.The compressive strength,scanning electron microscopy,energy dispersive spectrometer,mercury intrusion porosimetry,X-ray diffraction,and thermogra-vimetric tests were carried out to investigate the effect of the composite alkali activator proportion on the compressive strength,micro-structure,and composition of the cemented rockfill.The calcium silicate hydrate(C–S–H)molecular model of cemented rockfill was con-structed to explore the fracture evolution of the nucleated molecular structure under tension.The results show that compressive strength initially increased and then decreased with the activator proportion,the optimal activator proportion of 1:2 resulted in a 31.25%increase in strength at 3 d.This reasonable activator proportion strengthens the pozzolanic effect of gangue,and consumes more calcium hydroxide to inhibit its agglomeration,ultimately achieving the densification of microstructure.The activator proportion inevitably substitutes calcium ions with sodium ions in the C–S–H molecular model.The 12%substitution of calcium ions increases the adhesion between silicon chain layers,which is beneficial to the interlayer stress transfer.This work proposes a method for preparing low-cost cemented rockfill from al-kali-activated gangue,which can be used for solid waste recycling and reducing cement consumption to achieve low-carbon goals.展开更多
Granite residual soil (GRS) is a type of weathering soil that can decompose upon contact with water, potentially causing geological hazards. In this study, cement, an alkaline solution, and glass fiber were used to re...Granite residual soil (GRS) is a type of weathering soil that can decompose upon contact with water, potentially causing geological hazards. In this study, cement, an alkaline solution, and glass fiber were used to reinforce GRS. The effects of cement content and SiO_(2)/Na2O ratio of the alkaline solution on the static and dynamic strengths of GRS were discussed. Microscopically, the reinforcement mechanism and coupling effect were examined using X-ray diffraction (XRD), micro-computed tomography (micro-CT), and scanning electron microscopy (SEM). The results indicated that the addition of 2% cement and an alkaline solution with an SiO_(2)/Na2O ratio of 0.5 led to the densest matrix, lowest porosity, and highest static compressive strength, which was 4994 kPa with a dynamic impact resistance of 75.4 kN after adding glass fiber. The compressive strength and dynamic impact resistance were a result of the coupling effect of cement hydration, a pozzolanic reaction of clay minerals in the GRS, and the alkali activation of clay minerals. Excessive cement addition or an excessively high SiO_(2)/Na2O ratio in the alkaline solution can have negative effects, such as the destruction of C-(A)-S-H gels by the alkaline solution and hindering the production of N-A-S-H gels. This can result in damage to the matrix of reinforced GRS, leading to a decrease in both static and dynamic strengths. This study suggests that further research is required to gain a more precise understanding of the effects of this mixture in terms of reducing our carbon footprint and optimizing its properties. The findings indicate that cement and alkaline solution are appropriate for GRS and that the reinforced GRS can be used for high-strength foundation and embankment construction. The study provides an analysis of strategies for mitigating and managing GRS slope failures, as well as enhancing roadbed performance.展开更多
The technology of solid-state lighting has developed for decades in various industries.Phosphor,as an element part,determines the application domain of lighting products.For instance,blue and redemitting phosphors are...The technology of solid-state lighting has developed for decades in various industries.Phosphor,as an element part,determines the application domain of lighting products.For instance,blue and redemitting phosphors are required in the process of plant supplementing light,arrow-band emitting phosphors are applied to backlight displays,etc.In this work,a Bi^(3+)-activated blue phosphor was obtained in a symmetrical and co mpact crystal structure of Gd3Sb07(GSO).Then,the co-doping strategy of alkali metal ions(Li^(+),Na^(+),and K^(+))was used to optimize the performance.The result shows that the photoluminescence intensity is increased by 2.1 times and 1.3 times respectively by introducing Li~+and K^(+)ions.Not only that,it also achieves narrow-band emitting with the full width of half-maximum(FWHM)reaching 42 nm through Na^(+)doping,and its excitation peak position also shifts from 322 to 375 nm,which can be well excited by near-ultraviolet(NUV)light emitting diode(LED)chips(365 nm).Meanwhile,the electroluminescence spectrum of GSO:0.6 mol%Bi^(3+),3 wt%Na^(+)matches up to 93.39%of the blue part of the absorption spectrum of chlorophyll a.In summary,the Bi^(3+)-activated blue phosphor reported in this work can synchronously meet the requirements of plant light replenishment and field emission displays.展开更多
In this study,the catalysis function of Na_(2)CO_(3) to the structural properties of xylan char was well investigated with Na_(2)CO_(3) on,and the electrochemical performance of xylan char as an anode material for sod...In this study,the catalysis function of Na_(2)CO_(3) to the structural properties of xylan char was well investigated with Na_(2)CO_(3) on,and the electrochemical performance of xylan char as an anode material for sodium-ion batteries was tested.The characterization of X-ray microscopy and scanning electron microscopy demonstrated that the morphological structure of xylan char was altered due to the addition of Na_(2)CO_(3) catalyst.The increasement of the Na_(2)CO_(3)/xylan ratio resulted in a slenderization of the triangular prism shape of the char skeleton and a reduction in porosity.X-ray diffraction analysis revealed that Na_(2)CO_(3) promoted the growth of the(004)crystal plane of graphite during xylan pyrolysis,while inhibiting the formation of the(100/101)crystal planes.Raman spectroscopy analysis indicated that the presence of Na_(2)CO_(3)had changed the graphitization degree of xylan char.Electrochemical tests further showed that char prepared with a Na_(2)CO_(3)/xylan mass ratio of 1∶1 exhibited the highest sodium storage capacity.This study provides a pathway for the rational design carbon materials derived from xylan for future applications in energy storage devices.展开更多
Chemical hydrogen storage in organic materials is a promising method thanks to its high storage density,reversibility,and safety.However,the dehydrogenation process of organic materials requires high temperatures due ...Chemical hydrogen storage in organic materials is a promising method thanks to its high storage density,reversibility,and safety.However,the dehydrogenation process of organic materials requires high temperatures due to their unfavorable thermodynamic properties.This study proposes a strategy to design a new type of hydrogen storage materials,i.e.,alkali metal pyridinolate/piperidinolate pairs,by combining the effects of a heteroatom and an alkali metal in one molecule to achieve suitable dehydrogenation thermodynamics along with high hydrogen storage capacities.These air-stable compounds can be synthesized using low-cost reactants and water as a green solvent.Thermodynamic predictions indicate that enthalpy changes of dehydrogenation(ΔH_(d))can be significantly reduced to the optimal range for efficient hydrogen release,exemplified by lithium 2-piperidinolate with a 5.6 wt%hydrogen capacity and a suitableΔH_(d)of 32.2 kJ/mol-H_(2).Experimental results obtained using sodium systems validate the computational predictions,demonstrating reversible hydrogen storage even below 100℃.The superior hydrogen desorption performance of alkali metal piperidinolates could be attributed to their suitableΔH_(d)induced by the combined effect of ring nitrogen and metal substitution on their structures.This study not only reports new low-cost hydrogen storage materials but also provides a rational design strategy for developing metalorganic compounds possessing high hydrogen capacities and suitable thermodynamics for efficient hydrogen storage.展开更多
Ln-containing polyoxoniobates(PONbs)have appealing applications in luminescence,information encryption and magnetic fields,but the synthesis of PONbs containing high-nuclearity Ln-O clusters is challenging due to the ...Ln-containing polyoxoniobates(PONbs)have appealing applications in luminescence,information encryption and magnetic fields,but the synthesis of PONbs containing high-nuclearity Ln-O clusters is challenging due to the easy hydrolysis of Ln^(3+)ions in alkaline environments.In this paper,we are able to integrate CO_(3)^(2-)and high-nuclearity Ln-O clusters into PONb to construct an inorganic giant Eu_(19)-embedded PONb H_(49)K_(16)Na_(13)(H_(2)O)_(63)[Eu_(21)O_(2)(OH)_(7)(H_(2)O)_(5)(Nb_(7)O_(22))_(10)(Nb_(2)O_(6))_(2)(CO_(3))_(18)]·91H_(2)O(1),which contains the highest nuclearity Eu-O clusters and the largest number of Eu^(3+)ions among PONbs.In addition,the film that was prepared by mixing 1 with gelatin and glycerol,exhibits reversible luminescence switching behavior under acid/alkali stimulation and has been used to create a fluorescence-encoded information approach.This work paves a feasible strategy for the construction of high-nuclearity Ln-O cluster-containing PONbs and the expansion of the application of Ln-containing PONbs in information encryption.展开更多
We read with great interest the investigations conducted by Pourakbar et al.(2024)on the“Stabilization of clay soil using alkali-activated sewage sludge.”The authors have investigated the feasibility of utilizing al...We read with great interest the investigations conducted by Pourakbar et al.(2024)on the“Stabilization of clay soil using alkali-activated sewage sludge.”The authors have investigated the feasibility of utilizing alkali-activated sewage sludge(AASS)as a binder for stabilizing the clayey soil.Sewage sludge(SS)in varying proportions of 1.5%,2%,2.5%,3.5%,and 4.5%was utilized to prepare geopolymer binders using sodium and potassium-based alkali activators.Furthermore,unconfined compressive strength(UCS)and direct shear tests were conducted to examine the strength development of clayey soil stabilized with AASS.While the study presented some intriguing results,we have identified critical concerns regarding(i)the selection of SS as a precursor for alkali activation,(ii)technical inconsistencies associated with the compaction characteristics and microstructural analysis,and(iii)the feasibility of the proposed methodology for practical applications.Through our discussion,we seek to highlight these issues and provide constructive feedback to advance the understanding of alkali activation processes and their implications for soil stabilization.展开更多
Among their several unique properties,the high electrical conductivity and mechanical strength of carbon nanofibers make them suitable for applications such as catalyst support for fuel cells,flexible electrode materi...Among their several unique properties,the high electrical conductivity and mechanical strength of carbon nanofibers make them suitable for applications such as catalyst support for fuel cells,flexible electrode materials for secondary batteries,and sensors.However,their performance requires improvement for practical applications.Several methods have been pursued to achieve this,such as growing carbon nanotubes from carbon nanofibers;however,the transition metal catalyst used to grow carbon nanotubes causes problems,including side reactions.This study attempts to address this issue by growing numerous branched carbon nanofibers from the main carbon nanofibers using alkali metals.Excellent electrical conductivity is achieved by growing densely branched carbon nanofibers.Consequently,a current collector,binder,and conductive material-free anode material is realized,exhibiting excellent electrochemical performance compared with existing carbon nanofibers.The proposed method is expected to be a powerful tool for secondary batteries and have broad applicability to various fields.展开更多
An efficient strategy has been developed to reconstruct chain folding and traversing of poly(L-lactide)(PLLA)during melt crystallization based on the selective hydrolysis of its amorphous regions.The molecular weights...An efficient strategy has been developed to reconstruct chain folding and traversing of poly(L-lactide)(PLLA)during melt crystallization based on the selective hydrolysis of its amorphous regions.The molecular weights of the pristine PLLA(crystalline part),single stem,and single cluster were determined by gel permeation chromatography(GPC)according to their evolution during alkali hydrolysis.The maximum-folding-number(in a single cluster)and minimum-cluster-number(in one polymer chain)were obtained using these molecular weights.With the help of two numbers,the chain folding and traversing during the melt crystallization process(at 120℃)of PLLA can be described as follows.Statistically,in a single polymer chain,there are at least 2 clusters consisting of up to 6.5 stems in each of them,while the rest of the polymer chain contributes to amorphous regions.Our results provide a new strategy for the investigation and fundamental understanding of the melt crystallization of PLLA.展开更多
The soot emitted during the operation of diesel engine exhaust seriously threatens the human health and environment,so treating diesel engine exhaust is critical.At present,the most effective method for eliminating so...The soot emitted during the operation of diesel engine exhaust seriously threatens the human health and environment,so treating diesel engine exhaust is critical.At present,the most effective method for eliminating soot particles is post-treatment technology.Preparation of economically viable and highly active soot combustion catalysts is a pivotal element of post-treatment technology.In this study,different single-metal oxide catalysts with fibrous structures and alkali metal-modified hollow nanotubular Mn-based oxide catalysts were synthesized using centrifugal spinning method.Activity evaluation results showed that the manganese oxide catalyst has the best catalytic activity among the prepared single-metal oxide catalysts.Further research on alkali metal modification showed that doping alkali metals is beneficial for improving the oxidation state of manganese and generating a large number of reactive oxygen species.Combined with the structural effect brought by the hollow nanotube structure,the alkali metal-modified Mn-based oxide catalysts exhibit superior catalytic performance.Among them,the Cs-modified Mn-based oxide catalyst exhibits the best catalytic performance because of its rich active oxygen species,excellent NO oxidation ability,abundant Mn^(4+)ions(M^(n4)+/Mn^(n+)=64.78%),and good redox ability.The T_(10),T_(50),T_(90),and CO_(2)selectivity of the Cs-modified Mn-based oxide catalyst were 267°C,324°C,360°C,and 97.8%,respectively.展开更多
Sulfur trioxide(SO_(3))as a condensable particle matter has a significant influence on atmospheric visibility,which easily arouses formation of haze.It is imperative to control the SO_(3)emission from the industrial f...Sulfur trioxide(SO_(3))as a condensable particle matter has a significant influence on atmospheric visibility,which easily arouses formation of haze.It is imperative to control the SO_(3)emission from the industrial flue gas.Three commonly used basic absorbents,including Ca(OH)_(2),MgO and NaHCO_(3)were selected to explore the effects of temperature,SO_(2)concentration on the SO_(3)absorption,and the reaction mechanism of SO_(3)absorption was further illustrated.The suitable reaction temperature for various absorbents were proposed,Ca(OH)_(2)at the high temperatures above 500°C,MgO at the low temperatures below 320°C,and NaHCO_(3)at the temperature range of 320–500°C.The competitive absorption between SO_(2)and SO_(3)was found that the addition of SO_(2)reduced the SO_(3)absorption on Ca(OH)_(2)and NaHCO_(3),while had no effect on MgO.The order of the absorption selectivity of SO_(3)follows MgO,NaHCO_(3)and Ca(OH)_(2)under the given conditions in this work.The absorption process of SO_(3)on NaHCO_(3)follows the shrinking core model,thus the absorption reaction continues until NaHCO_(3)was exhausted with the utilization rate of nearly 100%.The absorption process of SO_(3)on Ca(OH)_(2)and MgO follows the grain model,and the dense product layer hinders the further absorption reaction,resulting in low utilization of about 50%for Ca(OH)_(2)and MgO.The research provides a favorable support for the selection of alkaline absorbent for SO_(3)removal in application.展开更多
Co-associated rare earth elements(lanthanide and yttrium,REY)in coal and its by-products have been considered important potential nontraditional rare earth sources.In this study,a coal gangue sample collected from a c...Co-associated rare earth elements(lanthanide and yttrium,REY)in coal and its by-products have been considered important potential nontraditional rare earth sources.In this study,a coal gangue sample collected from a coal processing plant in Jinsha County of Guizhou Province,southwest China,was used as the research object.The content,modes of occurrence,and extraction(acid leaching after pretreatment of selective grinding,tailings discarding,and alkali roasting)of REY from the sample were analyzed.The result shows that the content of REY(1038.26μg/g)in pyrite and quartz is low but mainly enriched in kaolinite.Under the following conditions of a filling ratio of 40%(grinding media steel ball)and grinding time of 8 min,selective grinding pretreatment is applied to achieve 176.95μg/g(yield 24.08%)and 1104.93μg/g(yield 75.92%)of REY in+2 mm and-2 mm fractions,respectively.Thus,the-2 mm coal gangue fraction is selected,used as the feed,and roasted and leached with HCl.When Na_(2)CO_(3)and NaCl are separately used as roasting activators,the REY leaching ratios are 91.41%and 68.88%,respectively,under the optimum conditions.The contents of REY in the final leachate are 1010.02 and 761.08μg/g when Na_(2)CO_(3)and NaCl are used,respectively.The two REY contents are relatively higher than the impurity ions in the leachate,which facilitates further REY separation.The mechanism study reveals that high-temperature roasting increases the pore size and the total pore area of the gangue,which promotes leachate penetration and improves reaction efficiency.In addition,roasting facilitates the reaction between the sodium salt activator and kaolinite and other aluminosilicate minerals in the coal gangue to generate soluble salts,thus releasing REY into the solution.The appropriate roasting temperature transforms the activator into a molten state.Thus,the reaction between coal gangue and activator is a solid-liquid reaction rather than a solid-solid reaction,which improves the efficiency of the chemical reaction.展开更多
Alkali metal batteries(AMBs)have undergone substantial development in portable devices due to their high energy density and durable cycle performance.However,with the rising demand for smart wearable electronic device...Alkali metal batteries(AMBs)have undergone substantial development in portable devices due to their high energy density and durable cycle performance.However,with the rising demand for smart wearable electronic devices,a growing focus on safety and durability becomes increasingly apparent.An effective strategy to address these increased requirements involves employing the quasi-solid gel electrolytes(QSGEs).This review focuses on the application of QSGEs in AMBs,emphasizing four types of gel electrolytes and their influence on battery performance and stability.First,self-healing gels are discussed to prolong battery life and enhance safety through self-repair mechanisms.Then,flexible gels are explored for their mechanical flexibility,making them suitable for wearable devices and flexible electronics.In addition,biomimetic gels inspired by natural designs are introduced for high-performance AMBs.Furthermore,biomass materials gels are presented,derived from natural biomaterials,offering environmental friendliness and biocompatibility.Finally,the perspectives and challenges for future developments are discussed in terms of enhancing the ionic conductivity,mechanical strength,and environmental stability of novel gel materials.The review underscores the significant contributions of these QSGEs in enhancing AMBs performance,including increased lifespan,safety,and adaptability,providing new insights and directions for future research and applications in the field.展开更多
基金supported by the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No.XDB1030000)the Beijing United Fund (Grant No.L252063)。
文摘Alkali metal thermochemical ablation is a promising anti-tumor therapy in which tumor tissue can be efficiently destroyed via both heat and hydroxyl ions released from the chemical reaction in tissue between an alkali metal and water. Encouraging results have been reported from in vitro and in vivo trials in a previous study. However, the precise process of heat and mass transfer triggered by the above thermochemical reaction in tumor tissue has still remained confusing. Here, to better understand the temperature and p H responses of tumor tissue subject to alkali metal therapy, a theoretical model coupling temperature and concentration field is developed for characterizing the physicochemical reaction and the transport process occurring around the inserted sodium capsule during treatment. Preliminary experiments in tumor tissue are performed to validate the theoretical predictions of temperature, and the results indicate that the bioheat transfer model can predict the temperature responses in the tissues heated by the sodium capsule very well. Furthermore, comprehensive parametric studies are performed to evaluate the effects of either physiological or physicochemical parameters, including ablation time, time lags, and blood perfusion rate. Based on the numerical results, useful instructions are suggested for planning alkali metal tumor ablation treatment.
基金Supported by the National Key Research Program(No.2024-1129-954-112)National Natural Science Foundation of China(No.52372033)Guangxi Science and Technology Major Program(No.AA24263054)。
文摘Alkali-free SiO_(2)-Al_(2)O_(3)-CaO-MgO with different SiO_(2)/Al_(2)O_(3)mass ratios was prepared by conventional melt quenching method.The glass network structure,thermodynamic properties and elastic modulus changes with SiO_(2)and Al_(2)O_(3)ratios were investigated using various techniques.It is found that when SiO_(2)is replaced by Al_(2)O_(3),the Q^(4) to Q^(3) transition of silicon-oxygen network decreases while the aluminum-oxygen network increases,which result in the transformation of Si-O-Si bonds to Si-O-Al bonds and an increase in glass network connectivity even though the intermolecular bond strength decreases.The glass transition temperature(T_(g))increases continuously,while the thermal expansion coefficient increases and high-temperature viscosity first decreases and then increases.Meanwhile,the elastic modulus values increase from 93 to 102 GPa.This indicates that the elastic modulus is mainly affected by packing factor and dissociation energy,and elements with higher packing factors and dissociation energies supplant those with lower values,resulting in increased rigidity within the glass.
基金Funded by Central Guiding Local Science and Technology Development Special Fund Project(No.ZYYD2023B02)Innovation and Entrepreneurship Training Program for College Students in Xinjiang Uygur Autonomous Region(No.S202410994015)+2 种基金China University of Mining and Technology Coal Fine Exploration and Intelligent Development National Key Laboratory Xinjiang Engineering College Joint Fund(No.SKLCRSM-XJIE24KF001)Basic Research Funds for Autonomous Region Universities(No.XJEDU2024P082)National Natural Science Foundation of China(No.41662017)。
文摘In order to realize the comprehensive utilization of industrial solid waste rice husk ash and heavy metal cadmium contaminated soil,rice husk ash-based geopolymer prepared by alkaline activator was used to modify cadmium contaminated soil.The main physical and chemical properties of rice husk ash were clarified by SEM,XRF and X-ray diffraction.The unconfined compressive strength test and toxicity leaching test were carried out on the modified soil.Combined with FTIR and TG micro-level,the solidification mechanism of rice husk ash-based geopolymer solidified cadmium contaminated soil was discussed.The results show that the strength of geopolymer modified soil is significantly higher than that of plain soil,and the unconfined compressive strength at 7 d age is 4.2 times that of plain soil.The strength of modified soil with different dosage of geopolymer at 28 d age is about 36% to 40% higher than that of modified soil at 7 d age.Geopolymer has a significant effect on the leaching of heavy metals in contaminated soil.When the cadmium content is 100 mg/kg,it meets the standard limit.In the process of complex depolymerization-condensation reaction,on the one hand,geopolymers are cemented and agglomerated to form a complex spatial structure,which affects the macro and micro characteristics of soil.On the other hand,it has significant adsorption,precipitation and replacement effects on heavy metal ions in soil,showing good strength and low heavy metal leaching toxicity.
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.
基金supported by the National Natural Science Foundation of China(52371131)the 10th Youth Talent Lifting Project of the China Association for Science and Technology.
文摘Rechargeable alkali metal-sulfur(M-S)batteries,including Li/Na/K-S chemistries,have the potential to utilize abundant and low-cost sulfur cathodes yet offer high theoretical energy densities.However,their practical electrochemical performance is fundamentally limited by the polysulfide shuttle effect.This challenge is particularly exacerbated in Na-S and K-S systems owing to larger metal-ion radii,weaker solvation energies,slower redox kinetics,and greater electrolyte-electrode incompatibilities compared to Li-S batteries.This review presents a comparative analysis of interface engineering strategies designed to suppress the shuttle effect across these three systems.Following a summary of sulfur cathode properties and reaction mechanisms,we systematically examine the origins of polysulfide shuttling.Our analysis progresses from functional separator design and interlayer enhancements to the implementation of solid-state electrolytes for root-cause inhibition.By evaluating interface engineering research specific to Na-S and K-S batteries,we elucidate both shared principles and unique challenges inherent to alkali M-S systems.Finally,we propose multifaceted solutions to achieve shuttlefree operation and enhance overall battery performance,thereby establishing a foundation for future advancements.
基金support from the National Natural Science Foundation of China(No.22175060).
文摘The hydrogen evolution reaction(HER)is crucial for hydrogen production and sustainable energy storage.Molybdenum disulfide(MoS_(2)),a representative transition metal dichalcogenides(TMDs),shows potential as an HER catalyst but suffers from limited performance due to poor charge transfer and interfacial effects.Here,we report a salt-assisted chemical vapor deposition(CVD)method for synthesizing high-quality tungsten ditelluride(WTe_(2))with tunable morphologies using alkali halides(NaCl,KCl and LiCl).The prepared WTe_(2) nanoribbons and hexagonal nanosheets exhibit morphology-dependent electrical conductivity,with nanosheets showing superior performance.To evaluate WTe_(2) as a contact electrode,WTe_(2)−MoS_(2) heterostructures were fabricated and compared with graphene-MoS_(2) counterparts.The WTe_(2)−MoS_(2) heterostructure exhibits a superior Tafel slope of 111.57 mV/dec and an overpotential of 298 mV at-10 mA/cm^(2),significantly outperforming graphene-based electrodes.This improvement is attributed to the excellent conductivity of WTe_(2) and reduced interfacial Schottky barriers.Moreover,we systematically investigate the influence of WTe_(2) thickness on HER performance and assess the electrochemical durability and structural stability of the heterostructure,further confirming the effectiveness of WTe_(2) as a contact electrode for enhancing the HER activity of MoS_(2).This study offers a novel approach for enhancing the HER performance of MoS_(2) through controlled WTe_(2) growth and application as a contact electrode.Our findings provide valuable insights into the synthesis of high-quality WTe_(2) and broaden the potential applications of two-dimensional materials in energy catalysis.
基金supported by the National Key R&D Program of China (Grant No.2022YFA1403201)the National Natural Science Foundation of China (Grant Nos.12125404,T2495231,123B2049,and 12204138)+9 种基金the Advanced MaterialsNational Science and Technology Major Project (Grant No.2024ZD0607000)the Natural Science Foundation of Jiangsu Province (Grant Nos.BK20233001 and BK20253009)the Jiangsu Funding Program for Excellent Postdoctoral Talent (Grant No.2024ZB002)the China Postdoctoral Science Foundation (Grant No.2025M773331)the Fundamental and Interdisciplinary Disciplines Breakthrough Plan of the Ministry of Education of Chinathe AI&AI for Science program of Nanjing UniversityArtificial Intelligence and Quantum physics (AIQ) program of Nanjing Universitythe Fundamental Research Funds for the Central Universitiesthe Natural Science Foundation of Nanjing University of Posts and Telecommunications(Grant Nos.NY224165,NY220038,and NY219087)the Hua Li Talents Program of Nanjing University of Posts and Telecommunications。
文摘We report a theoretical investigation into superconductivity within the MAXH_(6) quaternary hydride system using first-principles calculations,where M and A denote alkali and alkaline earth elements,respectively,and X represents transition metal elements.Systematic analysis of electronic band structures,phonon dispersions,and electron-phonon coupling reveals that substitution of MA binary metal combinations and X metal atoms can create favorable conditions for superconductivity.Mapping of superconducting critical temperatures,combined with dynamical stability analysis through phonon calculations,identifies ten superconducting candidates at ambient pressure.Among these,LiNaAgH_(6) exhibits nearly-free-electron behavior reminiscent of monovalent electron superconductors.It demonstrates exceptional superconducting properties with electron–phonon coupling λ=2.707,which yields a superconducting transition temperature T_(c) of 206.4 K using the Allen–Dynes formula.Its structural analogs MgNaPdH_(6),LiMgPdH_(6),LiMgAgH_(6),LiMgAuH_(6) all exhibit superconducting transition temperatures above 110 K.These findings advance our fundamental understanding of superconductivity in quaternary hydrides and provide guidance for rational design of new high-temperature superconducting materials.
基金supported by the Key Research and Development Special Tasks of Xinjiang,China (No.2022B01051-2)the National Natural Science Foundation of China (Nos.U23B2091,42372328,and 52478253)+1 种基金the Natural Science Foundation of Jiangsu Province,China (No.BK20240209)the Science and Technology Program Special Fund of Jiangsu Province (Frontier Leading Technology Basic Research) Major projects,China (No.BK 20222004)
文摘Using cemented rockfill to replace coal pillars offers an effective solution for reducing solid waste while ensuring the safety of gob-side entries.However,achieving the balance among low cost,high waste recycling rates,and adequate strength remains a significant challenge for cemented rockfill.This study used a composite alkali activator to activate gangue cemented rockfill.The compressive strength,scanning electron microscopy,energy dispersive spectrometer,mercury intrusion porosimetry,X-ray diffraction,and thermogra-vimetric tests were carried out to investigate the effect of the composite alkali activator proportion on the compressive strength,micro-structure,and composition of the cemented rockfill.The calcium silicate hydrate(C–S–H)molecular model of cemented rockfill was con-structed to explore the fracture evolution of the nucleated molecular structure under tension.The results show that compressive strength initially increased and then decreased with the activator proportion,the optimal activator proportion of 1:2 resulted in a 31.25%increase in strength at 3 d.This reasonable activator proportion strengthens the pozzolanic effect of gangue,and consumes more calcium hydroxide to inhibit its agglomeration,ultimately achieving the densification of microstructure.The activator proportion inevitably substitutes calcium ions with sodium ions in the C–S–H molecular model.The 12%substitution of calcium ions increases the adhesion between silicon chain layers,which is beneficial to the interlayer stress transfer.This work proposes a method for preparing low-cost cemented rockfill from al-kali-activated gangue,which can be used for solid waste recycling and reducing cement consumption to achieve low-carbon goals.
基金the support provided by the National Natural Science Foundation of China(Grant Nos.52278336 and 42302032)Guangdong Basic and Applied Research Foundation(Grant Nos.2023B1515020061).
文摘Granite residual soil (GRS) is a type of weathering soil that can decompose upon contact with water, potentially causing geological hazards. In this study, cement, an alkaline solution, and glass fiber were used to reinforce GRS. The effects of cement content and SiO_(2)/Na2O ratio of the alkaline solution on the static and dynamic strengths of GRS were discussed. Microscopically, the reinforcement mechanism and coupling effect were examined using X-ray diffraction (XRD), micro-computed tomography (micro-CT), and scanning electron microscopy (SEM). The results indicated that the addition of 2% cement and an alkaline solution with an SiO_(2)/Na2O ratio of 0.5 led to the densest matrix, lowest porosity, and highest static compressive strength, which was 4994 kPa with a dynamic impact resistance of 75.4 kN after adding glass fiber. The compressive strength and dynamic impact resistance were a result of the coupling effect of cement hydration, a pozzolanic reaction of clay minerals in the GRS, and the alkali activation of clay minerals. Excessive cement addition or an excessively high SiO_(2)/Na2O ratio in the alkaline solution can have negative effects, such as the destruction of C-(A)-S-H gels by the alkaline solution and hindering the production of N-A-S-H gels. This can result in damage to the matrix of reinforced GRS, leading to a decrease in both static and dynamic strengths. This study suggests that further research is required to gain a more precise understanding of the effects of this mixture in terms of reducing our carbon footprint and optimizing its properties. The findings indicate that cement and alkaline solution are appropriate for GRS and that the reinforced GRS can be used for high-strength foundation and embankment construction. The study provides an analysis of strategies for mitigating and managing GRS slope failures, as well as enhancing roadbed performance.
基金Project supported by the Key R&D Projects in Hunan Province(2021SK2047,2022NK2044)Science and Technology Innovation Program of Hunan Province(2022WZ1022)Superior Youth Project of the Science Research Project of Hunan Provincial Department of Education(22B0211)。
文摘The technology of solid-state lighting has developed for decades in various industries.Phosphor,as an element part,determines the application domain of lighting products.For instance,blue and redemitting phosphors are required in the process of plant supplementing light,arrow-band emitting phosphors are applied to backlight displays,etc.In this work,a Bi^(3+)-activated blue phosphor was obtained in a symmetrical and co mpact crystal structure of Gd3Sb07(GSO).Then,the co-doping strategy of alkali metal ions(Li^(+),Na^(+),and K^(+))was used to optimize the performance.The result shows that the photoluminescence intensity is increased by 2.1 times and 1.3 times respectively by introducing Li~+and K^(+)ions.Not only that,it also achieves narrow-band emitting with the full width of half-maximum(FWHM)reaching 42 nm through Na^(+)doping,and its excitation peak position also shifts from 322 to 375 nm,which can be well excited by near-ultraviolet(NUV)light emitting diode(LED)chips(365 nm).Meanwhile,the electroluminescence spectrum of GSO:0.6 mol%Bi^(3+),3 wt%Na^(+)matches up to 93.39%of the blue part of the absorption spectrum of chlorophyll a.In summary,the Bi^(3+)-activated blue phosphor reported in this work can synchronously meet the requirements of plant light replenishment and field emission displays.
基金supported by the Foundation Project of Jihua Laboratory(X200191TL200).
文摘In this study,the catalysis function of Na_(2)CO_(3) to the structural properties of xylan char was well investigated with Na_(2)CO_(3) on,and the electrochemical performance of xylan char as an anode material for sodium-ion batteries was tested.The characterization of X-ray microscopy and scanning electron microscopy demonstrated that the morphological structure of xylan char was altered due to the addition of Na_(2)CO_(3) catalyst.The increasement of the Na_(2)CO_(3)/xylan ratio resulted in a slenderization of the triangular prism shape of the char skeleton and a reduction in porosity.X-ray diffraction analysis revealed that Na_(2)CO_(3) promoted the growth of the(004)crystal plane of graphite during xylan pyrolysis,while inhibiting the formation of the(100/101)crystal planes.Raman spectroscopy analysis indicated that the presence of Na_(2)CO_(3)had changed the graphitization degree of xylan char.Electrochemical tests further showed that char prepared with a Na_(2)CO_(3)/xylan mass ratio of 1∶1 exhibited the highest sodium storage capacity.This study provides a pathway for the rational design carbon materials derived from xylan for future applications in energy storage devices.
基金partially supported by the National Key R&D Program of China(2023YFE0198900)support provided by the National Natural Science Foundation of China(52171226,22309174)。
文摘Chemical hydrogen storage in organic materials is a promising method thanks to its high storage density,reversibility,and safety.However,the dehydrogenation process of organic materials requires high temperatures due to their unfavorable thermodynamic properties.This study proposes a strategy to design a new type of hydrogen storage materials,i.e.,alkali metal pyridinolate/piperidinolate pairs,by combining the effects of a heteroatom and an alkali metal in one molecule to achieve suitable dehydrogenation thermodynamics along with high hydrogen storage capacities.These air-stable compounds can be synthesized using low-cost reactants and water as a green solvent.Thermodynamic predictions indicate that enthalpy changes of dehydrogenation(ΔH_(d))can be significantly reduced to the optimal range for efficient hydrogen release,exemplified by lithium 2-piperidinolate with a 5.6 wt%hydrogen capacity and a suitableΔH_(d)of 32.2 kJ/mol-H_(2).Experimental results obtained using sodium systems validate the computational predictions,demonstrating reversible hydrogen storage even below 100℃.The superior hydrogen desorption performance of alkali metal piperidinolates could be attributed to their suitableΔH_(d)induced by the combined effect of ring nitrogen and metal substitution on their structures.This study not only reports new low-cost hydrogen storage materials but also provides a rational design strategy for developing metalorganic compounds possessing high hydrogen capacities and suitable thermodynamics for efficient hydrogen storage.
基金the financial support from the National Natural Science Foundation of China(Nos.21971040,22171045,and 22371046)。
文摘Ln-containing polyoxoniobates(PONbs)have appealing applications in luminescence,information encryption and magnetic fields,but the synthesis of PONbs containing high-nuclearity Ln-O clusters is challenging due to the easy hydrolysis of Ln^(3+)ions in alkaline environments.In this paper,we are able to integrate CO_(3)^(2-)and high-nuclearity Ln-O clusters into PONb to construct an inorganic giant Eu_(19)-embedded PONb H_(49)K_(16)Na_(13)(H_(2)O)_(63)[Eu_(21)O_(2)(OH)_(7)(H_(2)O)_(5)(Nb_(7)O_(22))_(10)(Nb_(2)O_(6))_(2)(CO_(3))_(18)]·91H_(2)O(1),which contains the highest nuclearity Eu-O clusters and the largest number of Eu^(3+)ions among PONbs.In addition,the film that was prepared by mixing 1 with gelatin and glycerol,exhibits reversible luminescence switching behavior under acid/alkali stimulation and has been used to create a fluorescence-encoded information approach.This work paves a feasible strategy for the construction of high-nuclearity Ln-O cluster-containing PONbs and the expansion of the application of Ln-containing PONbs in information encryption.
文摘We read with great interest the investigations conducted by Pourakbar et al.(2024)on the“Stabilization of clay soil using alkali-activated sewage sludge.”The authors have investigated the feasibility of utilizing alkali-activated sewage sludge(AASS)as a binder for stabilizing the clayey soil.Sewage sludge(SS)in varying proportions of 1.5%,2%,2.5%,3.5%,and 4.5%was utilized to prepare geopolymer binders using sodium and potassium-based alkali activators.Furthermore,unconfined compressive strength(UCS)and direct shear tests were conducted to examine the strength development of clayey soil stabilized with AASS.While the study presented some intriguing results,we have identified critical concerns regarding(i)the selection of SS as a precursor for alkali activation,(ii)technical inconsistencies associated with the compaction characteristics and microstructural analysis,and(iii)the feasibility of the proposed methodology for practical applications.Through our discussion,we seek to highlight these issues and provide constructive feedback to advance the understanding of alkali activation processes and their implications for soil stabilization.
基金supported by the Ministry of Education of the Republic of Korea and the National Research Foundation of Korea(NRF2023R1A2C2004191)supported by Korea Basic Science Institute(National research Facilities and Equipment Center)grant funded by Ministry of Education(grant No.2022R1A6C101B738).
文摘Among their several unique properties,the high electrical conductivity and mechanical strength of carbon nanofibers make them suitable for applications such as catalyst support for fuel cells,flexible electrode materials for secondary batteries,and sensors.However,their performance requires improvement for practical applications.Several methods have been pursued to achieve this,such as growing carbon nanotubes from carbon nanofibers;however,the transition metal catalyst used to grow carbon nanotubes causes problems,including side reactions.This study attempts to address this issue by growing numerous branched carbon nanofibers from the main carbon nanofibers using alkali metals.Excellent electrical conductivity is achieved by growing densely branched carbon nanofibers.Consequently,a current collector,binder,and conductive material-free anode material is realized,exhibiting excellent electrochemical performance compared with existing carbon nanofibers.The proposed method is expected to be a powerful tool for secondary batteries and have broad applicability to various fields.
基金financially supported by"Pioneer"and"Leading Goose"R&D Program of Zhejiang(No.2023C03130)the National Natural Science Foundation of China(No.22373029)+1 种基金Interdisciplinary Research Project of Hangzhou Normal University(No.2024JCXK02)Open Project Program of Key Laboratory of Yarn Materials Forming and Composite Processing Technology of Zhejiang Province(No.MTC2022-09)。
文摘An efficient strategy has been developed to reconstruct chain folding and traversing of poly(L-lactide)(PLLA)during melt crystallization based on the selective hydrolysis of its amorphous regions.The molecular weights of the pristine PLLA(crystalline part),single stem,and single cluster were determined by gel permeation chromatography(GPC)according to their evolution during alkali hydrolysis.The maximum-folding-number(in a single cluster)and minimum-cluster-number(in one polymer chain)were obtained using these molecular weights.With the help of two numbers,the chain folding and traversing during the melt crystallization process(at 120℃)of PLLA can be described as follows.Statistically,in a single polymer chain,there are at least 2 clusters consisting of up to 6.5 stems in each of them,while the rest of the polymer chain contributes to amorphous regions.Our results provide a new strategy for the investigation and fundamental understanding of the melt crystallization of PLLA.
基金supported by National Key R&D Program of China(2022YFB3506200,2022YFB3504100)National Natural Science Foundation of China(22072095,22372107,22202058)+3 种基金Excellent Youth Science Foundation of Liaoning Province(2022-YQ-20)Shenyang Science and Technology Planning Project(22-322-3-28)Liaoning Xingliao talented youth Top talent program(XLYC2203007)University Joint Education Project for China-Central and Eastern European Countries(2021097).
文摘The soot emitted during the operation of diesel engine exhaust seriously threatens the human health and environment,so treating diesel engine exhaust is critical.At present,the most effective method for eliminating soot particles is post-treatment technology.Preparation of economically viable and highly active soot combustion catalysts is a pivotal element of post-treatment technology.In this study,different single-metal oxide catalysts with fibrous structures and alkali metal-modified hollow nanotubular Mn-based oxide catalysts were synthesized using centrifugal spinning method.Activity evaluation results showed that the manganese oxide catalyst has the best catalytic activity among the prepared single-metal oxide catalysts.Further research on alkali metal modification showed that doping alkali metals is beneficial for improving the oxidation state of manganese and generating a large number of reactive oxygen species.Combined with the structural effect brought by the hollow nanotube structure,the alkali metal-modified Mn-based oxide catalysts exhibit superior catalytic performance.Among them,the Cs-modified Mn-based oxide catalyst exhibits the best catalytic performance because of its rich active oxygen species,excellent NO oxidation ability,abundant Mn^(4+)ions(M^(n4)+/Mn^(n+)=64.78%),and good redox ability.The T_(10),T_(50),T_(90),and CO_(2)selectivity of the Cs-modified Mn-based oxide catalyst were 267°C,324°C,360°C,and 97.8%,respectively.
基金supported by the National Natural Science Foundation of China(No.52000172)the National Key R&D Program of China(Nos.2017YFB0304300 and 2017YFB0304303).
文摘Sulfur trioxide(SO_(3))as a condensable particle matter has a significant influence on atmospheric visibility,which easily arouses formation of haze.It is imperative to control the SO_(3)emission from the industrial flue gas.Three commonly used basic absorbents,including Ca(OH)_(2),MgO and NaHCO_(3)were selected to explore the effects of temperature,SO_(2)concentration on the SO_(3)absorption,and the reaction mechanism of SO_(3)absorption was further illustrated.The suitable reaction temperature for various absorbents were proposed,Ca(OH)_(2)at the high temperatures above 500°C,MgO at the low temperatures below 320°C,and NaHCO_(3)at the temperature range of 320–500°C.The competitive absorption between SO_(2)and SO_(3)was found that the addition of SO_(2)reduced the SO_(3)absorption on Ca(OH)_(2)and NaHCO_(3),while had no effect on MgO.The order of the absorption selectivity of SO_(3)follows MgO,NaHCO_(3)and Ca(OH)_(2)under the given conditions in this work.The absorption process of SO_(3)on NaHCO_(3)follows the shrinking core model,thus the absorption reaction continues until NaHCO_(3)was exhausted with the utilization rate of nearly 100%.The absorption process of SO_(3)on Ca(OH)_(2)and MgO follows the grain model,and the dense product layer hinders the further absorption reaction,resulting in low utilization of about 50%for Ca(OH)_(2)and MgO.The research provides a favorable support for the selection of alkaline absorbent for SO_(3)removal in application.
基金Project supported by the National Natural Science Foundation of China(51964009)。
文摘Co-associated rare earth elements(lanthanide and yttrium,REY)in coal and its by-products have been considered important potential nontraditional rare earth sources.In this study,a coal gangue sample collected from a coal processing plant in Jinsha County of Guizhou Province,southwest China,was used as the research object.The content,modes of occurrence,and extraction(acid leaching after pretreatment of selective grinding,tailings discarding,and alkali roasting)of REY from the sample were analyzed.The result shows that the content of REY(1038.26μg/g)in pyrite and quartz is low but mainly enriched in kaolinite.Under the following conditions of a filling ratio of 40%(grinding media steel ball)and grinding time of 8 min,selective grinding pretreatment is applied to achieve 176.95μg/g(yield 24.08%)and 1104.93μg/g(yield 75.92%)of REY in+2 mm and-2 mm fractions,respectively.Thus,the-2 mm coal gangue fraction is selected,used as the feed,and roasted and leached with HCl.When Na_(2)CO_(3)and NaCl are separately used as roasting activators,the REY leaching ratios are 91.41%and 68.88%,respectively,under the optimum conditions.The contents of REY in the final leachate are 1010.02 and 761.08μg/g when Na_(2)CO_(3)and NaCl are used,respectively.The two REY contents are relatively higher than the impurity ions in the leachate,which facilitates further REY separation.The mechanism study reveals that high-temperature roasting increases the pore size and the total pore area of the gangue,which promotes leachate penetration and improves reaction efficiency.In addition,roasting facilitates the reaction between the sodium salt activator and kaolinite and other aluminosilicate minerals in the coal gangue to generate soluble salts,thus releasing REY into the solution.The appropriate roasting temperature transforms the activator into a molten state.Thus,the reaction between coal gangue and activator is a solid-liquid reaction rather than a solid-solid reaction,which improves the efficiency of the chemical reaction.
基金support from the Postgraduate Research&Practice Innovation Program of Jiangsu Province(Yangzhou University)(KYCX23_3508)the Yangzhou University International Academic Exchange Fund.Prof.Guoxiu Wang acknowledges the Australian Research Council(ARC)Linkage project(LP200200926).
文摘Alkali metal batteries(AMBs)have undergone substantial development in portable devices due to their high energy density and durable cycle performance.However,with the rising demand for smart wearable electronic devices,a growing focus on safety and durability becomes increasingly apparent.An effective strategy to address these increased requirements involves employing the quasi-solid gel electrolytes(QSGEs).This review focuses on the application of QSGEs in AMBs,emphasizing four types of gel electrolytes and their influence on battery performance and stability.First,self-healing gels are discussed to prolong battery life and enhance safety through self-repair mechanisms.Then,flexible gels are explored for their mechanical flexibility,making them suitable for wearable devices and flexible electronics.In addition,biomimetic gels inspired by natural designs are introduced for high-performance AMBs.Furthermore,biomass materials gels are presented,derived from natural biomaterials,offering environmental friendliness and biocompatibility.Finally,the perspectives and challenges for future developments are discussed in terms of enhancing the ionic conductivity,mechanical strength,and environmental stability of novel gel materials.The review underscores the significant contributions of these QSGEs in enhancing AMBs performance,including increased lifespan,safety,and adaptability,providing new insights and directions for future research and applications in the field.
