The Xiangshan mafic-ultramafic complex is one of the major Early Permian maficultramafic intrusions in eastern Tianshan （Xinjiang, NW China）, and consists of two major intrusive phases. The first intrusive phase is ...The Xiangshan mafic-ultramafic complex is one of the major Early Permian maficultramafic intrusions in eastern Tianshan （Xinjiang, NW China）, and consists of two major intrusive phases. The first intrusive phase is mainly gabbroic rocks hosting ilmenite mineralization, while the second intrusive phase is mainly lherzoilite associated with Ni-Cu sulfide mineralization. The Xiangshan ilmenite orebodies hosted in the Fe-Ti oxide-bearing gabbro occur along the contact between hornblende gabbros and leucogabbros. The hornblende gabbros and Fe-Ti oxide rich gabbros at Xiangshan are newly dated to be Early Permian （280.1 and 279.2 Ma, respectively）. Major and trace element compositions of zircons and whole rocks from Xiangshan hornblende gabbro and Fe-Ti oxide gabbro have been measured by in situ excimer laser ablation ICP-MS. Zircon Ce^4＋/Ce^3＋ ratios based on lattice-strain model and Ti-in-zircon temperatures of hornblende gabbro and Fe-Ti oxide gabbro of the Xiangshan complex are calculated to evaluate the physicochemical variations during the ilmenite mineralization. Whole-rock geochemistry and zircon trace element geochemistry suggest that Fe-Ti oxide gabbros were formed from a basaltic parent magma which had undergone a transfromation from being H2O-rich to H2O-poor. During the magmatic evolution, primitive, HEO-poor basaltic melts may have been replenished into the system, increasing its solidus temperature and decreasing its oxygen fugacity and H2O contents. This may have supperessed the Ti-rich poikilitic hornblende fractionation and promoted the plagioclase fractionation, which consequently concentrated the ore-forming components in the residual melts and generated the ilmenite mineralization.展开更多
Recent work on the Panzhihua intrusion has produced two separate models for the crystallisation of the intrusion：（1） low-Ti,high CaO and low H2O（0.5 wt.%） parent magma（equivalent to Emeishan low-Ti basalt） at F...Recent work on the Panzhihua intrusion has produced two separate models for the crystallisation of the intrusion：（1） low-Ti,high CaO and low H2O（0.5 wt.%） parent magma（equivalent to Emeishan low-Ti basalt） at FMQ;and（2） high-Ti,low CaO and higher H2O（＆gt;1.5 wt.%） parent magma（equivalent to Emeishan high-Ti basalt） at FMQ ＋ 1.5.Modelling of these parent magma compositions produces significantly different results. We present here detailed f（O2） and H2O modelling for average compositions of both Emeishan high-Ti and low-Ti ferrobasalts in order to constrain the effects on crystallisation sequences for Emeishan ultra-mafic -mafic layered intrusions.Modelling is consistent with numerous experimental studies on ferro-basaltic magmas from other localities（e.g.Skaergaard intrusion）.Modelling is compared with the geology of the Panzhihua intrusion in order to constrain the crystallisation of the gabbroic rocks and the Fe-Ti oxides ore layers.We suggest that the gabbroic rocks at the Panzhihua intrusion can be best explained by crystallisation from a parent magma similar to that of the high-Ti Emeishan basalt at moderate H2O contents（0.5-1 wt.%） but at the lower end of TiO2 content for typical high-Ti basalts（2.5 wt.%TiO2）. Distinct silicate disequilibrium textures in the Fe-Ti oxide ore layers suggest that an influx of H2O may be responsible for changing the crystallisation path.An increase in H2O during crystallisation of gabbroic rocks will result in the depression of silicate liquidus temperatures and resultant disequilibrium with the liquid.Continued cooling of the magma with high H2O then results in precipitation of Mt-Uv alone. The H2O content of parent magmas for mafic layered intrusions associated with the ELIP is an important variable.H2O alters the crystallisation sequence of the basaltic magmas so that at high H2O and f（O2） Mt -Uv crystallises earlier than plagioclase and clinopyroxene.Furthermore,the addition of H2O to an anhydrous magma can explain silicate disequilibrium texture observed in the Fe-Ti oxide ore layers.展开更多
Magmatic Ni-Cu-(PGE) sulfide and Fe-Ti oxide deposits in plume-related large igneous provinces(LIPs)are commonly related to low-Ti and high-Ti series magmas, respectively, but the major factors that control such a rel...Magmatic Ni-Cu-(PGE) sulfide and Fe-Ti oxide deposits in plume-related large igneous provinces(LIPs)are commonly related to low-Ti and high-Ti series magmas, respectively, but the major factors that control such a relationship of metallogenic types and magma compositions are unclear. Magma fOcontrols sulfur status and relative timing of Fe-Ti oxide saturation in mafic magmas, which may help clarify this issue. Taking the Emeishan LIP as a case, we calculated the magma fOof the high-Ti and low-Ti picrites based on the olivine-spinel oxygen barometer, and the partitioning of V in olivine. The obtained fOof the high-Ti series magma(FMQ + 1.1 to FMQ + 2.6) is higher than that of the low-Ti series magma(FMQ-0.5to FMQ + 0.5). The magma fOof the high-Ti and low-Ti picrites containing Fo > 90 olivine reveals that the mantle source of the high-Ti series is likely more oxidized than that of the low-Ti series. The results using the ’lambda REE’ approach show that the high-Ti series may have been derived from relatively oxidized mantle with garnet pyroxenite component. The S contents at sulfide saturation(SCSS) of the two series magmas were calculated based on liquid compositions obtained from the alpha Melts modeling, and the results show that the low-Ti series magma could easily attain the sulfide saturation as it has low fOwith S being dominantly as S. In contrast, the oxidized high-Ti series magma is difficult to attain the sulfide saturation, but could crystallize Fe-Ti oxides at magma MgO content of ~7.0 wt.%. Thus, contrasting magma fOof low-Ti and high-Ti series in plume-related LIPs may play an important role in producing two different styles of metallogeny.展开更多
The Niumaoquan layered gabbroic intrusion is in the southern margin of the Central Asian Orogenic Belt in North Xinjiang, China, and hosts a Fe-Ti oxide deposit in its evolved gabbroic phases. In this paper, we report...The Niumaoquan layered gabbroic intrusion is in the southern margin of the Central Asian Orogenic Belt in North Xinjiang, China, and hosts a Fe-Ti oxide deposit in its evolved gabbroic phases. In this paper, we report zircon U-Pb age, Sr-Nd-Hf isotopes, plagioclase chemistry, and whole-rock geochemistry of the Niumaoquan layered gabbroic intrusion. Zircon grains separated from an anorthosite sample analyzed by laser ablation inductively coupled plasma mass spectrometry yielded a concordia age of 314.7±0.74 Ma, indicating that the Niumaoquan ore-bearing gabbroic intrusion was emplaced during the Late Carboniferous. The olivine gabbro texture and plagioclase chemistry suggest that plagioclase was an early crystallized silicate phase that crystallized prior to olivine. Fractional crystallization and accumulation of plagioclase significantly controlled the evolution of the Niumaoquan gabbroic intrusion and contributed to the formation of anorthosite layers, causing metallogenic elements to become enriched in the residual melt. The Niumaoquan gabbroic intrusion is characterized by the enrichment of large ion lithophile elements and depletion of high field strength elements, positive zircon εHf（t） values（＋2.1 to ＋12.2）, positive εNd（t） values（＋3.3 to ＋5.2）, and low initial ^（87）Sr/^（86）Sr ratios（0.7039 to 0.7047）, suggesting that the parental magma was produced by interactions between metasomatized lithospheric mantle and depleted asthenospheric melts at an early post-collision stage. The Fe-Ti oxide mineralization of the Niumaoquan intrusion benefited from interactions between depleted asthenospheric melts and lithospheric mantle, and fractional crystallization of abundant plagioclase and magnesian minerals.展开更多
A series of crystallization experiments have been carried out by using natural Emeishan Ti-rich hydrous basalts as starting materials at a pressure of 0.5 GPa and temperatures of 800-1000℃to constrain the origin of F...A series of crystallization experiments have been carried out by using natural Emeishan Ti-rich hydrous basalts as starting materials at a pressure of 0.5 GPa and temperatures of 800-1000℃to constrain the origin of Fe-Ti-V oxide ore deposits.Our experimental results demonstrate that the sandwich-and trellis-type ilmenite lamellae in titanomagnetite of layered intrusions can be formed by the reaction of earlier crystallized ilmenite and the evolved parental magma.During evolution of parental basaltic magma,the Fe-Ti oxide should be composed of titanomagnetite+ilmenite in the earlier stage,but changed to titanomagnetite+titanomagnetite-ilmenite intergrowth±ilmenite at the later stage.Accordingly,the Panzhihua Fe-Ti oxide ores,which are mainly composed of titanomagnetite,should be formed earlier than the adjacent gabbro,in which titanomagnetite-ilmenite intergrowth is the major form of the Fe-Ti oxide.展开更多
The Panzhihua mafic intrusion,which hosts a world-class Fe-Ti-V ore deposit,is in the western Emeishan region,SW China.The formation age(~260 Ma),and Sr and Nd isotopes indicate that the Panzhihua intrusion is part of...The Panzhihua mafic intrusion,which hosts a world-class Fe-Ti-V ore deposit,is in the western Emeishan region,SW China.The formation age(~260 Ma),and Sr and Nd isotopes indicate that the Panzhihua intrusion is part of the Emeishan large igneous province and has little crustal contamination.To assess ore genesis of the Panzhihua Fe-Ti-V ore deposit,two different models have been provided to explain the formation,namely silicate immiscibility and normal fractional crystallization.Silicate immiscibility occurring around 1,000℃at the late stage of basaltic magma evolution argues against the silicate immiscibility model.Apatite-hosted melt inclusion research indicates that silicate immiscibility occurred at the late stage of Panzhihua magma evolution,which may not have offered potential to form such large ore deposits as Panzhihua.Alternatively,continuous compositional variations of the Panzhihua intrusion and calculations using thermodynamic modelling software support the hypothesis that the Panzhihua deposit was formed by normal fractional crystallization.Reciprocal trace element patterns of the Panzhihua intrusion and nearby felsic rocks also coincide with the fractional crystallization model.Normal fractional crystallization of high-Ti basaltic magma played a key role in the formation of the Panzhihua Fe-Ti-V ore deposit.展开更多
The mafic-ultramafic intrusion in the XV anomaly area,contains magmatic Fe-Ti oxides±(p)ore,is located in the Bafq mining district in the Central Iran.It consists of cumulate and layered Fe-Ti-bearing gabbros and...The mafic-ultramafic intrusion in the XV anomaly area,contains magmatic Fe-Ti oxides±(p)ore,is located in the Bafq mining district in the Central Iran.It consists of cumulate and layered Fe-Ti-bearing gabbros and pyroxenites.The mineral assemblages include clinopyroxene,Fe-Ti oxides,plagioclase,amphibole,apatite and sulfides(pyrite and chalcopyrite).The Fe-Ti oxides mainly consist of magnetite-titanomagnetite and ilmenite,which occurred as disseminated,intergrowth,lamellae(trellis and sandwich textures)and inclusions.Magnetite in the gabbroic rocks is from the near end-member of Fe_(3)O_(4)(<1 wt.%TiO_(2))to titanomagnetite containing up to 8 wt.%TiO_(2)(about3.73 wt.%to 26.84 wt.%Ulvospinel(X_(Usp))).Magnetite in pyroxenite rocks is characterized with TiO_(2)range from 0.46 wt.%to 3.14 wt.%(X_(Usp)varied from 1.76 wt.%to 10.46 wt.%).The abundances of V_(2)O_(3)range from 0.03 wt.%to 1.29 wt.%and 0.24 wt.%to 1.00 wt.%for gabbro and pyroxenite,respectively.X_(Usp)contents of magnetite show insignificant correlations with Al_(2)O_(3)and MgO.The average XIlmin the ilmenite of gabbro is 92%,whereas it is 90.37%in the pyroxenite rocks.The MgO and V_(2)O_(3)contents show a slightly positive correlation with TiO_(2)in ilmenite.The composition of clinopyroxenes in gabbro and pyroxenite rocks fall in the diopside to augite field with Mg#ranging from 67 to 98 and 74 to 96,respectively.In both rock types,amphiboles are mainly pargasite and rarely actinolite.Plagioclase in pyroxenite rocks is clustered in the labradorite to andesine fields with a compositional ranges of An46-69and in gabboic rocks fall in two fields with compositional ranges of albite with An0.65-5.95and labradorite with An50-63.Theδ34S isotopic values cover a limited range from+3.15‰to+4.10‰V-CDT consistent with magmatic origin.Fe-Ti mineralization is formed in two stages,minor inclusions of Fe-Ti oxide minerals in the pyroxene and plagioclase crystallized in the early magmatic stage,whereas interstitial oxides formed by fractional crystallization processes that accumulated by gravitational settling in the later stage as intercumulus phase.Gravitational settling process is supported by the observation of decreasing the amount of Fe-Ti oxides from Fe-Ti oxide-rich pyroxenite to weak mineralized gabbro(base to top).The high contents of H2O,phosphorate and high initial Ti-Fe in parental magma are the crucial factors controlling the Fe-Ti oxides enrichment and mineralization.展开更多
Propylene oxide(PO)is an important petrochemical materials used to produce downstream products such as propylene glycol(PG),polyether polyols,and dipropylene glycol(DPG).Among these,DPG is commonly used as a solvent f...Propylene oxide(PO)is an important petrochemical materials used to produce downstream products such as propylene glycol(PG),polyether polyols,and dipropylene glycol(DPG).Among these,DPG is commonly used as a solvent for fragrances,cosmetics,food additives,and detergents,and can also be served as a moisturizer in cosmetics,showing broad application prospects.The distribution of DPG isomers in the products synthesized from PO and PG has a significant impactΔrGΔrHΔfHθΔfGθPO+PG⇌DPG PO+DPG⇌TPG PG+PG⇌DPG+H_(2)O PG+DPG⇌TPG+H_(2)O on the quality of the products.Therefore,conducting thermodynamic calculation on the reaction of PO and PG to synthesize DPG can provide a theoretical basis for practical operations and product distribution regulation.So,in this paper,the thermodynamic parameters of PO,1,2-PG,H_(2)O,tripropylene glycol(TPG)and three isomers of DPG under different reaction conditions is calculated.Additionally,the,and lnK for four potential reactions at various reaction temperatures and pressures are calculated.By designing isodesmic reactions and combining the results of thermodynamic calculations,the and for the isomers of DPG are obtained,and the relative error is less than 7%.The results show that in the process of preparing DPG by PO and PG,when PO∶PG=1,the reaction temperature ranges from 298.15 to 413.15 K,and the pressure ranges from 101.325 to 506.625 kPa,the reactions of and are thermodynamically spontaneous.While the reactions of and are thermodynamically unspontaneous.The optimal reaction temperature and pressure are 413.15 K and 101.325 kPa.The thermodynamic stability of the three isomers is DPG1>DPG2>DPG3 under standard conditions.The accuracy of the computational results is verified through experimental design,and based on this,the factors affecting product distribution are analyzed.展开更多
Black nickel coatings have emerged as a research hotspot in materials science due to their excellent performance and broad application prospects.In this study,nickel-based black coatings were fabricated on low-carbon ...Black nickel coatings have emerged as a research hotspot in materials science due to their excellent performance and broad application prospects.In this study,nickel-based black coatings were fabricated on low-carbon steel substrates via photo-assisted electrodeposition.A systematic investigation was conducted on the effects of cerium ion concentration and nano-ceria(CeO_(2))particle content in the electrolyte on the coating properties,along with an analysis of the temporal evolution of coating’s corrosion resistance.When the cerium ion concentration in the electrolyte was 0.05 mol/L,the coating exhibited a uniform black appearance with a light absorption rate of 95%,an emissivity of 0.87,maximum impedance,and the lowest corrosion tendency,demonstrating optimal comprehensive performance.The coating prepared with a nano-ceria concentration of 6 g/L in the electrolyte exhibited an emissivity of 0.9,achieved a 5B adhesion grade(ASTM D3359-09),and demonstrated a one-order-of-magnitude reduction in corrosion current density compared to coatings fabricated without nano-ceria in the electrolyte.With prolonged storage time,the coating's impedance slightly increased,leading to improved corrosion resistance.展开更多
It is crucial to develop arsenic removal adsorbents with strong sulfur resistance under middle-low-temperature flue gas conditions(<400℃).In this work,five Fe-Ce-La oxides were prepared by co-precipitation method,...It is crucial to develop arsenic removal adsorbents with strong sulfur resistance under middle-low-temperature flue gas conditions(<400℃).In this work,five Fe-Ce-La oxides were prepared by co-precipitation method,and FeCeLaO/SiO_(2)-Al_(2)O_(3) composite adsorbents were prepared by coupling fly ash-based Si-Al carriers.The active components Fe-Ce-La oxides and Si-Al carriers were characterized by TPD,TG,XRF,BET and XPS,respectively.The effects of temperature,Si/Al ratio and FeCeLaO loading rate on the sulfur resistance were investigated.Results show that the SO_(2) promotes the arsenic removal of Fe_(2)O_(3),CeLaO and FeCeLaO.At 400℃,the arsenic removal efficiencies of the three oxides increase from 45.3%,72.5% and 81.3% without SO_(2) to 62.6%,80.5%and 91.0%,respectively.The SO_(2) inhibits the arsenic removal of La_(2)O_(2)CO_(3) and FeLaO,and the inhibition effect is pronounced at high temperatures.The sulfur poisoning resistance of Si-Al carriers increases with the increase of Si/Al ratio.When the Si/Al ratio is increased to 9.74,the arsenic removal efficiency in the SO_(2) environment is 13.9% higher than that in the absence of SO_(2).Introducing FeCeLaO active components is beneficial for enhancing the SO_(2) poisoning resistance of Si-Al carriers.The strong sulfur resistance of the FeCeLaO/SiO_(2)-Al_(2)O_(3) composite adsorbent results from multiple factors:protective effects of Ce on Fe,La and Al;sulfation-induced generation of Ce^(3+)and surface-adsorbed oxygen;and strong surface acidity of SiO_(2).展开更多
High-entropy oxides(HEOs)have emerged as a promising class of memristive materials,characterized by entropy-stabilized crystal structures,multivalent cation coordination,and tunable defect landscapes.These intrinsic f...High-entropy oxides(HEOs)have emerged as a promising class of memristive materials,characterized by entropy-stabilized crystal structures,multivalent cation coordination,and tunable defect landscapes.These intrinsic features enable forming-free resistive switching,multilevel conductance modulation,and synaptic plasticity,making HEOs attractive for neuromorphic computing.This review outlines recent progress in HEO-based memristors across materials engineering,switching mechanisms,and synaptic emulation.Particular attention is given to vacancy migration,phase transitions,and valence-state dynamics—mechanisms that underlie the switching behaviors observed in both amorphous and crystalline systems.Their relevance to neuromorphic functions such as short-term plasticity and spike-timing-dependent learning is also examined.While encouraging results have been achieved at the device level,challenges remain in conductance precision,variability control,and scalable integration.Addressing these demands a concerted effort across materials design,interface optimization,and task-aware modeling.With such integration,HEO memristors offer a compelling pathway toward energy-efficient and adaptable brain-inspired electronics.展开更多
Improving device efficiency is fundamental for advancing energy harvesting technology,particularly in systems designed to convert light energy into electrical output.In our previous studies,we developed a basic struct...Improving device efficiency is fundamental for advancing energy harvesting technology,particularly in systems designed to convert light energy into electrical output.In our previous studies,we developed a basic structure light pressure electric generator(Basic-LPEG),which utilized a layered configuration of Ag/Pb(Zr,Ti)O_(3)(PZT)/Pt/GaAs to generate electricity based on light-induced pressure on the PZT.In this study,we sought to enhance the performance of this Basic-LPEG by introducing Ag nanoparticles/graphene oxide(AgNPs/GO)composite units(NP-LPEG),creating upgraded harvesting device.Specifically,by depositing the AgNPs/GO units twice onto the Basic-LPEG,we observed an increase in output voltage and current from 241 mV and 3.1μA to 310 mV and 9.3μA,respectively,under a solar simulator.The increase in electrical output directly correlated with the intensity of the light pressure impacting the PZT,as well as matched the Raman measurements,finite-difference time-domain simulations,and COMSOL Multiphysics Simulation.Experimental data revealed that the enhancement in electrical output was proportional to the number of hot spots generated between Ag nanoparticles,where the electric field experienced substantial amplification.These results underline the effectiveness of AgNPs/GO units in boosting the light-induced electric generation capacity,thereby providing a promising pathway for high-efficiency energy harvesting devices.展开更多
Poly(phenylene oxide)(PPO)exhibits excellent dielectric properties,making it an ideal substrate for high-frequency,high-speed copper-clad laminates.The phenolic hydroxyl group at the end of PPO plays a key role in its...Poly(phenylene oxide)(PPO)exhibits excellent dielectric properties,making it an ideal substrate for high-frequency,high-speed copper-clad laminates.The phenolic hydroxyl group at the end of PPO plays a key role in its reactivity.Accurately quantifying the phenolic hydroxyl content in PPO is essential but challenging.In this study,we proposed a method for measuring the phenolic hydroxyl content of PPO using differential UV absorption spectroscopy.In alkaline solutions,the phenolic hydroxyl in PPO completely ionizes to form phenoxide ions,leading to a significant increase in UV absorbance at approximately 250 and 300 nm.Notably,the differential UV absorbance at approximately 300 nm was directly proportional to the phenolic hydroxyl concentration.Using 2,6-dimethylphenol as a standard,a calibration curve was established to relate the phenolic hydroxyl concentration to differential UV absorbance at approximately 300 nm,providing a precise and straightforward method for phenolic hydroxyl quantification in PPO with distinct advantages over conventional techniques.展开更多
Magnetic resonance imaging(MRI)is one of the most widely used diagnostic techniques.Iron oxide nanoparticles,as a promising kind of contrast agents,have attracted intense research interest due to their low toxicity an...Magnetic resonance imaging(MRI)is one of the most widely used diagnostic techniques.Iron oxide nanoparticles,as a promising kind of contrast agents,have attracted intense research interest due to their low toxicity and superparamagnetism.However,it is still a great challenge to prepare ideal iron oxide based contrast agents with high uniformity,excellent water solubility and biocompatibility.In this paper,a novel water-soluble polymer ligand pentaerythritol tetrakis 3-mercaptopropionate-poly(N-vinyl-2-pyrrolidone)(PTMP-PVP)was used as a capping reagent to prepare iron oxide nanoparticles MIONs@PTMP-PVP through one-step co-precipitation of iron precursors in aqueous solution at 100℃.The obtained nanoparticles MIONs@PTMP-PVP had a small size and narrow size distribution,and they were found to be biocompatible as determined through CCK-8 assay and histology analysis.In vivo MRI study demonstrated that the obtained MIONs@PTMP-PVP can be potentially used as an effective T_(2)-weighted MRI contrast agent.展开更多
Artificial intelligence(AI)based models have been used to predict the structural,optical,mechanical,and electrochemical properties of zinc oxide/graphene oxide nanocomposites.Machine learning(ML)models such as Artific...Artificial intelligence(AI)based models have been used to predict the structural,optical,mechanical,and electrochemical properties of zinc oxide/graphene oxide nanocomposites.Machine learning(ML)models such as Artificial Neural Networks(ANN),Support Vector Regression(SVR),Multilayer Perceptron(MLP),and hybrid,along with fuzzy logic tools,were applied to predict the different properties like wavelength at maximum intensity(444 nm),crystallite size(17.50 nm),and optical bandgap(2.85 eV).While some other properties,such as energy density,power density,and charge transfer resistance,were also predicted with the help of datasets of 1000(80:20).In general,the energy parameters were predicted more accurately by hybrid models.The hydrothermal method was used to synthesize graphene oxide(GO)and zinc oxide(ZnO)nanocomposites.The increased surface area,conductivity,and stability of graphene oxide in zinc oxide nanoparticles make the composite an ideal option for energy storage.X-ray diffraction(XRD)confirmed the crystallite size of 17.41 nm for the nanocomposite and the presence of GO(12.8○)peaks.The scanning electron microscope(SEM)showed anchored wrinkled GO sheets on zinc oxide with an average particle size of 2.93μm.Energy-dispersive X-ray spectroscopy(EDX)confirmed the elemental composition,and Fouriertransform infrared spectroscopy(FTIR)revealed the impact of GO on functional groups and electrochemical behavior.Photoluminescence(PL)wavelength of(439 nm)and band gap of(2.81 eV)show that the material is suitable for energy applications in nanocomposites.Smart nanocomposite materials with improved performance in energy storage and related applications were fabricated by combining synthesis,characterization,fuzzy logic,and machine learning in this work.展开更多
The thermal decomposition characteristic of ammonium perchlorate(AP)represents a critical factor in determining the performance of solid propellants,which has aroused significant interest on the structure and performa...The thermal decomposition characteristic of ammonium perchlorate(AP)represents a critical factor in determining the performance of solid propellants,which has aroused significant interest on the structure and performance improvement of kinds of catalysts.In this study,bimetallic metal-organic frameworks(MOFs),such as CuCo-BTC(BTC=1,3,5-Benzenetricarboxylic acid,H_(3)BTC),CuNi-BTC,and CoNi-BTC,were synthesized by solvothermal(ST)and spray-drying(SD)methods,and then calcined at 400℃for 2 h to form metal oxides.The catalysts as well as their catalytic effects for AP decomposition were characterized by FTIR,XRD,SEM,XPS,TG,DSC,TG-IR,EIS,CV,and LSV.It was found that the rapid coordination of metal ions with ligands during spray drying may lead to catalytic structural defects,promoting the exposure of reactive active sites and increasing the catalytic active region.The results showed that the addition of 2 wt%binary transition metal oxides(BTMOs)as catalysts significantly reduced the high-temperature decomposition(HTD)temperature of AP and enhanced its heat release.Of particular significance is the observation that SD-CoNiO_(x),prepared by spray-drying,reduced the decomposition temperature of AP from 413.26℃(pure AP)to 306℃and enhanced the heat release from 256.79 J/g(pure AP)to 1496.82 J/g,while concomitantly reducing the activation energy by 42%.By analysing the gaseous products during the decomposition of AP+SD-CoNiO_(x)and AP+ST-CoNiO_(x),it was found that SD-CoNiO_(x)could significantly increase the content of high-valent nitrogen oxides during the AP decomposition reaction,which indicates that the BTMOs prepared by spray-drying in the reaction system are more conducive to accelerating the electron transfer in the thermal decomposition process of AP,and can provide a high concentration of reactive oxygen species that oxidize AP to high-valent nitrogen oxide-containing compounds.The present study shows that the structure selectivity of the spray-drying technique influences surfactant molecular arrangement on catalyst surfaces,resulting in their ability to promote higher electron transfer during the catalytic process.Therefore,BTMOs prepared by spray drying method have higher potential for application.展开更多
This study focused on improving the cathode performance of Ba_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.15)O_(3-δ)(BSCN)-based perovskite materials through molybdenum(Mo)doping.Pure BSCN and Mo-modified-BSCN—Ea_(0.6)Sr_(0.4)Co_(0...This study focused on improving the cathode performance of Ba_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.15)O_(3-δ)(BSCN)-based perovskite materials through molybdenum(Mo)doping.Pure BSCN and Mo-modified-BSCN—Ea_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.1)Mo_(0.05)O_(3-δ)(B S CNM_(0.05)),Ba_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.05)Mo_(0.1)O_(3-δ)(BSCNM_(0.1)),and Ba_(0.6)Sr_(0.4)Co_(0.85)Mo_(0.15)O_(3-δ)(BSCM)—with Mo doping contents of 5mol%,10mol%,and15mol%,respectively,were successfully prepared using the sol-gel method.The effects of Mo doping on the crystal structure,conductivity,thermal expansion coefficient,oxygen reduction reaction(ORR)activity,and electrochemical performance were systematically evaluated using X-ray diffraction analysis,thermally induced characterization,electrochemical impedance spectroscopy,and single-cell performance tests.The results revealed that Mo doping could improve the conductivity of the materials,suppress their thermal expansion effects,and significantly improve the electrochemical performance.Surface chemical state analysis using X-ray photoelectron spectroscopy revealed that 5mol%Mo doping could facilitate a high adsorbed oxygen concentration leading to enhanced ORR activity in the materials.Density functional theory calculations confirmed that Mo doping promoted the ORR activity in the materials.At an operating temperature of 600℃,the BSCNM_(0.05)cathode material exhibited significantly enhanced electrochemical impedance characteristics,with a reduced area specific resistance of 0.048Ω·cm~2,which was lower than that of the undoped BSCN matrix material by 32.39%.At the same operating temperature,an anode-supported single cell using a BSCNM_(0.05)cathode achieved a peak power density of 1477 mW·cm^(-2),which was 30.71%,56.30%,and 171.50%higher than those of BSCN,BSCNM_(0.1),and B SCM,respectively.The improved ORR activity and electrochemical performance of BSCNM_(0.05)indicate that it can be used as a cathode material in low-temperature solid oxide fuel cells.展开更多
Oxide dispersion strengthened(ODS)alloys are extensively used owing to high thermostability and creep strength contributed from uniformly dispersed fine oxides particles.However,the existence of these strengthening pa...Oxide dispersion strengthened(ODS)alloys are extensively used owing to high thermostability and creep strength contributed from uniformly dispersed fine oxides particles.However,the existence of these strengthening particles also deteriorates the processability and it is of great importance to establish accurate processing maps to guide the thermomechanical processes to enhance the formability.In this study,we performed particle swarm optimization-based back propagation artificial neural network model to predict the high temperature flow behavior of 0.25wt%Al2O3 particle-reinforced Cu alloys,and compared the accuracy with that of derived by Arrhenius-type constitutive model and back propagation artificial neural network model.To train these models,we obtained the raw data by fabricating ODS Cu alloys using the internal oxidation and reduction method,and conducting systematic hot compression tests between 400 and800℃with strain rates of 10^(-2)-10 S^(-1).At last,processing maps for ODS Cu alloys were proposed by combining processing parameters,mechanical behavior,microstructure characterization,and the modeling results achieved a coefficient of determination higher than>99%.展开更多
In coal mining on a high-pressure Ordovician limestone aquifer,grouting materials should have sufficient mechanical properties,particularly strong interfacial bonding performance to address stress concentration at the...In coal mining on a high-pressure Ordovician limestone aquifer,grouting materials should have sufficient mechanical properties,particularly strong interfacial bonding performance to address stress concentration at the grout-limestone interface induced by rock stress disturbances during mining.In this study,graphene oxide(GO)was integrated into cement-polyacrylate composite grout to improve its interfacial bonding.First,four-point bending tests were conducted,and the Monte Carlo method combined with the simplex search algorithm was employed to determine the variations in shear cohesion and static friction parameters.The results reveal that GO can significantly increase both the tensile and shear cohesion of the grout-limestone interface,but minimally affects the interfacial friction coefficient.Second,nuclear magnetic resonance(NMR)and scanning electron microscopy(SEM)tests were performed.The results indicate that GO nanosheets result in a squamaceous microstructure of the grout consolidation mass,increasing the adhesion of the grout-limestone interface.Moreover,spiny Aft(ettringite)clusters can be induced in limestone fracture surfaces by GO,which could serve as anchors for limestone and grout consolidation mass.展开更多
As the chemical industry expands,the use of benzene,toluene,and xylene(collectively known as BTX)in industrial production has increased greatly.Meanwhile,the toxic nature and potential health hazards of BTX gases cann...As the chemical industry expands,the use of benzene,toluene,and xylene(collectively known as BTX)in industrial production has increased greatly.Meanwhile,the toxic nature and potential health hazards of BTX gases cannot be ignored due to low-concentration leaks underline the critical need for rapid and real-time monitoring of these gases.Chemiresistive metal oxide semiconductor(MOS)-based gas sensors,which are extensively used for gas detection in both industrial settings and everyday life,emerge as one of the optimal solutions for trace BTX detection.These sensors are highly valued for their high sensitivity and low detection limits.Nevertheless,the improvement of selectivity towards specific BTX gases to achieve efficient and precise detection still remains challenging.This review summarizes the chemiresistive MOS-based gas sensors designed for BTX detection,categorizing them based on the components of sensing materials-basically into three groups:single-component,single heterojunction,and multiple heterojunctions gas sensing materials.Further,the review proposes the future application prospects of chemiresistive MOS-based BTX gas sensors,with specific emphasis on their significance in promoting industrial safety and environmental monitoring.展开更多
基金financially supported by the National Natural Science Foundation of China(No.41372102)the National Basic Research Program of China(No.2014CB440803)the China Geological Survey(No.DD20160071)
文摘The Xiangshan mafic-ultramafic complex is one of the major Early Permian maficultramafic intrusions in eastern Tianshan （Xinjiang, NW China）, and consists of two major intrusive phases. The first intrusive phase is mainly gabbroic rocks hosting ilmenite mineralization, while the second intrusive phase is mainly lherzoilite associated with Ni-Cu sulfide mineralization. The Xiangshan ilmenite orebodies hosted in the Fe-Ti oxide-bearing gabbro occur along the contact between hornblende gabbros and leucogabbros. The hornblende gabbros and Fe-Ti oxide rich gabbros at Xiangshan are newly dated to be Early Permian （280.1 and 279.2 Ma, respectively）. Major and trace element compositions of zircons and whole rocks from Xiangshan hornblende gabbro and Fe-Ti oxide gabbro have been measured by in situ excimer laser ablation ICP-MS. Zircon Ce^4＋/Ce^3＋ ratios based on lattice-strain model and Ti-in-zircon temperatures of hornblende gabbro and Fe-Ti oxide gabbro of the Xiangshan complex are calculated to evaluate the physicochemical variations during the ilmenite mineralization. Whole-rock geochemistry and zircon trace element geochemistry suggest that Fe-Ti oxide gabbros were formed from a basaltic parent magma which had undergone a transfromation from being H2O-rich to H2O-poor. During the magmatic evolution, primitive, HEO-poor basaltic melts may have been replenished into the system, increasing its solidus temperature and decreasing its oxygen fugacity and H2O contents. This may have supperessed the Ti-rich poikilitic hornblende fractionation and promoted the plagioclase fractionation, which consequently concentrated the ore-forming components in the residual melts and generated the ilmenite mineralization.
基金funding through South African National Science Foundation(NRF)Grant SA/China Project 67220 to SP and Mei-Fu ZhouGH also acknowledges the support of a doctoral fellowship from the NRF for 2011-2012
文摘Recent work on the Panzhihua intrusion has produced two separate models for the crystallisation of the intrusion：（1） low-Ti,high CaO and low H2O（0.5 wt.%） parent magma（equivalent to Emeishan low-Ti basalt） at FMQ;and（2） high-Ti,low CaO and higher H2O（＆gt;1.5 wt.%） parent magma（equivalent to Emeishan high-Ti basalt） at FMQ ＋ 1.5.Modelling of these parent magma compositions produces significantly different results. We present here detailed f（O2） and H2O modelling for average compositions of both Emeishan high-Ti and low-Ti ferrobasalts in order to constrain the effects on crystallisation sequences for Emeishan ultra-mafic -mafic layered intrusions.Modelling is consistent with numerous experimental studies on ferro-basaltic magmas from other localities（e.g.Skaergaard intrusion）.Modelling is compared with the geology of the Panzhihua intrusion in order to constrain the crystallisation of the gabbroic rocks and the Fe-Ti oxides ore layers.We suggest that the gabbroic rocks at the Panzhihua intrusion can be best explained by crystallisation from a parent magma similar to that of the high-Ti Emeishan basalt at moderate H2O contents（0.5-1 wt.%） but at the lower end of TiO2 content for typical high-Ti basalts（2.5 wt.%TiO2）. Distinct silicate disequilibrium textures in the Fe-Ti oxide ore layers suggest that an influx of H2O may be responsible for changing the crystallisation path.An increase in H2O during crystallisation of gabbroic rocks will result in the depression of silicate liquidus temperatures and resultant disequilibrium with the liquid.Continued cooling of the magma with high H2O then results in precipitation of Mt-Uv alone. The H2O content of parent magmas for mafic layered intrusions associated with the ELIP is an important variable.H2O alters the crystallisation sequence of the basaltic magmas so that at high H2O and f（O2） Mt -Uv crystallises earlier than plagioclase and clinopyroxene.Furthermore,the addition of H2O to an anhydrous magma can explain silicate disequilibrium texture observed in the Fe-Ti oxide ore layers.
基金supported by grants from the National Natural Science Foundation of China (Nos. 41902077, 41730423 and 41921003)China Postdoctoral Science Foundation Grant (No. 2019M653103)Science and Technology Planning of Guangdong Province, China (2020B1212060055)。
文摘Magmatic Ni-Cu-(PGE) sulfide and Fe-Ti oxide deposits in plume-related large igneous provinces(LIPs)are commonly related to low-Ti and high-Ti series magmas, respectively, but the major factors that control such a relationship of metallogenic types and magma compositions are unclear. Magma fOcontrols sulfur status and relative timing of Fe-Ti oxide saturation in mafic magmas, which may help clarify this issue. Taking the Emeishan LIP as a case, we calculated the magma fOof the high-Ti and low-Ti picrites based on the olivine-spinel oxygen barometer, and the partitioning of V in olivine. The obtained fOof the high-Ti series magma(FMQ + 1.1 to FMQ + 2.6) is higher than that of the low-Ti series magma(FMQ-0.5to FMQ + 0.5). The magma fOof the high-Ti and low-Ti picrites containing Fo > 90 olivine reveals that the mantle source of the high-Ti series is likely more oxidized than that of the low-Ti series. The results using the ’lambda REE’ approach show that the high-Ti series may have been derived from relatively oxidized mantle with garnet pyroxenite component. The S contents at sulfide saturation(SCSS) of the two series magmas were calculated based on liquid compositions obtained from the alpha Melts modeling, and the results show that the low-Ti series magma could easily attain the sulfide saturation as it has low fOwith S being dominantly as S. In contrast, the oxidized high-Ti series magma is difficult to attain the sulfide saturation, but could crystallize Fe-Ti oxides at magma MgO content of ~7.0 wt.%. Thus, contrasting magma fOof low-Ti and high-Ti series in plume-related LIPs may play an important role in producing two different styles of metallogeny.
基金financially supported by the National Natural Science Foundation of China(41372102)Chinese Geological Survey Project(DD20160071)
文摘The Niumaoquan layered gabbroic intrusion is in the southern margin of the Central Asian Orogenic Belt in North Xinjiang, China, and hosts a Fe-Ti oxide deposit in its evolved gabbroic phases. In this paper, we report zircon U-Pb age, Sr-Nd-Hf isotopes, plagioclase chemistry, and whole-rock geochemistry of the Niumaoquan layered gabbroic intrusion. Zircon grains separated from an anorthosite sample analyzed by laser ablation inductively coupled plasma mass spectrometry yielded a concordia age of 314.7±0.74 Ma, indicating that the Niumaoquan ore-bearing gabbroic intrusion was emplaced during the Late Carboniferous. The olivine gabbro texture and plagioclase chemistry suggest that plagioclase was an early crystallized silicate phase that crystallized prior to olivine. Fractional crystallization and accumulation of plagioclase significantly controlled the evolution of the Niumaoquan gabbroic intrusion and contributed to the formation of anorthosite layers, causing metallogenic elements to become enriched in the residual melt. The Niumaoquan gabbroic intrusion is characterized by the enrichment of large ion lithophile elements and depletion of high field strength elements, positive zircon εHf（t） values（＋2.1 to ＋12.2）, positive εNd（t） values（＋3.3 to ＋5.2）, and low initial ^（87）Sr/^（86）Sr ratios（0.7039 to 0.7047）, suggesting that the parental magma was produced by interactions between metasomatized lithospheric mantle and depleted asthenospheric melts at an early post-collision stage. The Fe-Ti oxide mineralization of the Niumaoquan intrusion benefited from interactions between depleted asthenospheric melts and lithospheric mantle, and fractional crystallization of abundant plagioclase and magnesian minerals.
基金supported by funds from the National Key Research and Development Program of China (No.2016YFC0600204)the National Natural Science Foundation of China (Nos.41530211 and41872061)+1 种基金the National Key Basic Research Program of China (No.2015CB856101)the MOST Special Fund from the State Key Laboratory of GPMR (No.MSFGPMR02-2)
文摘A series of crystallization experiments have been carried out by using natural Emeishan Ti-rich hydrous basalts as starting materials at a pressure of 0.5 GPa and temperatures of 800-1000℃to constrain the origin of Fe-Ti-V oxide ore deposits.Our experimental results demonstrate that the sandwich-and trellis-type ilmenite lamellae in titanomagnetite of layered intrusions can be formed by the reaction of earlier crystallized ilmenite and the evolved parental magma.During evolution of parental basaltic magma,the Fe-Ti oxide should be composed of titanomagnetite+ilmenite in the earlier stage,but changed to titanomagnetite+titanomagnetite-ilmenite intergrowth±ilmenite at the later stage.Accordingly,the Panzhihua Fe-Ti oxide ores,which are mainly composed of titanomagnetite,should be formed earlier than the adjacent gabbro,in which titanomagnetite-ilmenite intergrowth is the major form of the Fe-Ti oxide.
基金co-supported by the China Geological Survey(Grant Nos.DD20230229,DD20190011,DD20221643)the National Key Research and Development Project of China(Grant No.2018YFC0603701)。
文摘The Panzhihua mafic intrusion,which hosts a world-class Fe-Ti-V ore deposit,is in the western Emeishan region,SW China.The formation age(~260 Ma),and Sr and Nd isotopes indicate that the Panzhihua intrusion is part of the Emeishan large igneous province and has little crustal contamination.To assess ore genesis of the Panzhihua Fe-Ti-V ore deposit,two different models have been provided to explain the formation,namely silicate immiscibility and normal fractional crystallization.Silicate immiscibility occurring around 1,000℃at the late stage of basaltic magma evolution argues against the silicate immiscibility model.Apatite-hosted melt inclusion research indicates that silicate immiscibility occurred at the late stage of Panzhihua magma evolution,which may not have offered potential to form such large ore deposits as Panzhihua.Alternatively,continuous compositional variations of the Panzhihua intrusion and calculations using thermodynamic modelling software support the hypothesis that the Panzhihua deposit was formed by normal fractional crystallization.Reciprocal trace element patterns of the Panzhihua intrusion and nearby felsic rocks also coincide with the fractional crystallization model.Normal fractional crystallization of high-Ti basaltic magma played a key role in the formation of the Panzhihua Fe-Ti-V ore deposit.
基金supported by the department of Geoscience,University of Nevada,Las Vegas,NV 89154,USAfinanced by the French Government Laboratory of Excellence Initiative(No.ANR-10-LABX-0006)the Region Auvergne and the European Regional Development Fund。
文摘The mafic-ultramafic intrusion in the XV anomaly area,contains magmatic Fe-Ti oxides±(p)ore,is located in the Bafq mining district in the Central Iran.It consists of cumulate and layered Fe-Ti-bearing gabbros and pyroxenites.The mineral assemblages include clinopyroxene,Fe-Ti oxides,plagioclase,amphibole,apatite and sulfides(pyrite and chalcopyrite).The Fe-Ti oxides mainly consist of magnetite-titanomagnetite and ilmenite,which occurred as disseminated,intergrowth,lamellae(trellis and sandwich textures)and inclusions.Magnetite in the gabbroic rocks is from the near end-member of Fe_(3)O_(4)(<1 wt.%TiO_(2))to titanomagnetite containing up to 8 wt.%TiO_(2)(about3.73 wt.%to 26.84 wt.%Ulvospinel(X_(Usp))).Magnetite in pyroxenite rocks is characterized with TiO_(2)range from 0.46 wt.%to 3.14 wt.%(X_(Usp)varied from 1.76 wt.%to 10.46 wt.%).The abundances of V_(2)O_(3)range from 0.03 wt.%to 1.29 wt.%and 0.24 wt.%to 1.00 wt.%for gabbro and pyroxenite,respectively.X_(Usp)contents of magnetite show insignificant correlations with Al_(2)O_(3)and MgO.The average XIlmin the ilmenite of gabbro is 92%,whereas it is 90.37%in the pyroxenite rocks.The MgO and V_(2)O_(3)contents show a slightly positive correlation with TiO_(2)in ilmenite.The composition of clinopyroxenes in gabbro and pyroxenite rocks fall in the diopside to augite field with Mg#ranging from 67 to 98 and 74 to 96,respectively.In both rock types,amphiboles are mainly pargasite and rarely actinolite.Plagioclase in pyroxenite rocks is clustered in the labradorite to andesine fields with a compositional ranges of An46-69and in gabboic rocks fall in two fields with compositional ranges of albite with An0.65-5.95and labradorite with An50-63.Theδ34S isotopic values cover a limited range from+3.15‰to+4.10‰V-CDT consistent with magmatic origin.Fe-Ti mineralization is formed in two stages,minor inclusions of Fe-Ti oxide minerals in the pyroxene and plagioclase crystallized in the early magmatic stage,whereas interstitial oxides formed by fractional crystallization processes that accumulated by gravitational settling in the later stage as intercumulus phase.Gravitational settling process is supported by the observation of decreasing the amount of Fe-Ti oxides from Fe-Ti oxide-rich pyroxenite to weak mineralized gabbro(base to top).The high contents of H2O,phosphorate and high initial Ti-Fe in parental magma are the crucial factors controlling the Fe-Ti oxides enrichment and mineralization.
基金Supported by the Natural Science Foundation of Shanxi Province(202203021221303)the Science and Technology Major Project of Shanxi Province(202005D121002)the Science and Technology Cooperation and Communication Project of Shanxi Province(202304041101016)。
文摘Propylene oxide(PO)is an important petrochemical materials used to produce downstream products such as propylene glycol(PG),polyether polyols,and dipropylene glycol(DPG).Among these,DPG is commonly used as a solvent for fragrances,cosmetics,food additives,and detergents,and can also be served as a moisturizer in cosmetics,showing broad application prospects.The distribution of DPG isomers in the products synthesized from PO and PG has a significant impactΔrGΔrHΔfHθΔfGθPO+PG⇌DPG PO+DPG⇌TPG PG+PG⇌DPG+H_(2)O PG+DPG⇌TPG+H_(2)O on the quality of the products.Therefore,conducting thermodynamic calculation on the reaction of PO and PG to synthesize DPG can provide a theoretical basis for practical operations and product distribution regulation.So,in this paper,the thermodynamic parameters of PO,1,2-PG,H_(2)O,tripropylene glycol(TPG)and three isomers of DPG under different reaction conditions is calculated.Additionally,the,and lnK for four potential reactions at various reaction temperatures and pressures are calculated.By designing isodesmic reactions and combining the results of thermodynamic calculations,the and for the isomers of DPG are obtained,and the relative error is less than 7%.The results show that in the process of preparing DPG by PO and PG,when PO∶PG=1,the reaction temperature ranges from 298.15 to 413.15 K,and the pressure ranges from 101.325 to 506.625 kPa,the reactions of and are thermodynamically spontaneous.While the reactions of and are thermodynamically unspontaneous.The optimal reaction temperature and pressure are 413.15 K and 101.325 kPa.The thermodynamic stability of the three isomers is DPG1>DPG2>DPG3 under standard conditions.The accuracy of the computational results is verified through experimental design,and based on this,the factors affecting product distribution are analyzed.
文摘Black nickel coatings have emerged as a research hotspot in materials science due to their excellent performance and broad application prospects.In this study,nickel-based black coatings were fabricated on low-carbon steel substrates via photo-assisted electrodeposition.A systematic investigation was conducted on the effects of cerium ion concentration and nano-ceria(CeO_(2))particle content in the electrolyte on the coating properties,along with an analysis of the temporal evolution of coating’s corrosion resistance.When the cerium ion concentration in the electrolyte was 0.05 mol/L,the coating exhibited a uniform black appearance with a light absorption rate of 95%,an emissivity of 0.87,maximum impedance,and the lowest corrosion tendency,demonstrating optimal comprehensive performance.The coating prepared with a nano-ceria concentration of 6 g/L in the electrolyte exhibited an emissivity of 0.9,achieved a 5B adhesion grade(ASTM D3359-09),and demonstrated a one-order-of-magnitude reduction in corrosion current density compared to coatings fabricated without nano-ceria in the electrolyte.With prolonged storage time,the coating's impedance slightly increased,leading to improved corrosion resistance.
文摘It is crucial to develop arsenic removal adsorbents with strong sulfur resistance under middle-low-temperature flue gas conditions(<400℃).In this work,five Fe-Ce-La oxides were prepared by co-precipitation method,and FeCeLaO/SiO_(2)-Al_(2)O_(3) composite adsorbents were prepared by coupling fly ash-based Si-Al carriers.The active components Fe-Ce-La oxides and Si-Al carriers were characterized by TPD,TG,XRF,BET and XPS,respectively.The effects of temperature,Si/Al ratio and FeCeLaO loading rate on the sulfur resistance were investigated.Results show that the SO_(2) promotes the arsenic removal of Fe_(2)O_(3),CeLaO and FeCeLaO.At 400℃,the arsenic removal efficiencies of the three oxides increase from 45.3%,72.5% and 81.3% without SO_(2) to 62.6%,80.5%and 91.0%,respectively.The SO_(2) inhibits the arsenic removal of La_(2)O_(2)CO_(3) and FeLaO,and the inhibition effect is pronounced at high temperatures.The sulfur poisoning resistance of Si-Al carriers increases with the increase of Si/Al ratio.When the Si/Al ratio is increased to 9.74,the arsenic removal efficiency in the SO_(2) environment is 13.9% higher than that in the absence of SO_(2).Introducing FeCeLaO active components is beneficial for enhancing the SO_(2) poisoning resistance of Si-Al carriers.The strong sulfur resistance of the FeCeLaO/SiO_(2)-Al_(2)O_(3) composite adsorbent results from multiple factors:protective effects of Ce on Fe,La and Al;sulfation-induced generation of Ce^(3+)and surface-adsorbed oxygen;and strong surface acidity of SiO_(2).
基金financially supported by the National Natural Science Foundation of China(Grant No.12172093)the Guangdong Basic and Applied Basic Research Foundation(Grant No.2021A1515012607)。
文摘High-entropy oxides(HEOs)have emerged as a promising class of memristive materials,characterized by entropy-stabilized crystal structures,multivalent cation coordination,and tunable defect landscapes.These intrinsic features enable forming-free resistive switching,multilevel conductance modulation,and synaptic plasticity,making HEOs attractive for neuromorphic computing.This review outlines recent progress in HEO-based memristors across materials engineering,switching mechanisms,and synaptic emulation.Particular attention is given to vacancy migration,phase transitions,and valence-state dynamics—mechanisms that underlie the switching behaviors observed in both amorphous and crystalline systems.Their relevance to neuromorphic functions such as short-term plasticity and spike-timing-dependent learning is also examined.While encouraging results have been achieved at the device level,challenges remain in conductance precision,variability control,and scalable integration.Addressing these demands a concerted effort across materials design,interface optimization,and task-aware modeling.With such integration,HEO memristors offer a compelling pathway toward energy-efficient and adaptable brain-inspired electronics.
基金supported by Korea Evaluation Institute of Industrial Technology(KEIT)grant funded by the Korea Government(MOTIE)(RS-2022-00154720,Technology Innovation Program Development of next-generation power semiconductor based on Si-on-SiC structure)the National Research Foundation of Korea(NRF)by the Korea government(RS-2023-NR076826)Global-Learning&Academic Research Institution for Master's·PhD students,and Postdocs(LAMP)Program of the National Research Foundation of Korea(NRF)by the Ministry of Education(No.RS-2024-00443714).
文摘Improving device efficiency is fundamental for advancing energy harvesting technology,particularly in systems designed to convert light energy into electrical output.In our previous studies,we developed a basic structure light pressure electric generator(Basic-LPEG),which utilized a layered configuration of Ag/Pb(Zr,Ti)O_(3)(PZT)/Pt/GaAs to generate electricity based on light-induced pressure on the PZT.In this study,we sought to enhance the performance of this Basic-LPEG by introducing Ag nanoparticles/graphene oxide(AgNPs/GO)composite units(NP-LPEG),creating upgraded harvesting device.Specifically,by depositing the AgNPs/GO units twice onto the Basic-LPEG,we observed an increase in output voltage and current from 241 mV and 3.1μA to 310 mV and 9.3μA,respectively,under a solar simulator.The increase in electrical output directly correlated with the intensity of the light pressure impacting the PZT,as well as matched the Raman measurements,finite-difference time-domain simulations,and COMSOL Multiphysics Simulation.Experimental data revealed that the enhancement in electrical output was proportional to the number of hot spots generated between Ag nanoparticles,where the electric field experienced substantial amplification.These results underline the effectiveness of AgNPs/GO units in boosting the light-induced electric generation capacity,thereby providing a promising pathway for high-efficiency energy harvesting devices.
基金the“Pioneer”and“Leading Goose”R&D Program of Zhejiang(No.2023C01072)the Institute of Zhejiang University-Quzhou for their financial support。
文摘Poly(phenylene oxide)(PPO)exhibits excellent dielectric properties,making it an ideal substrate for high-frequency,high-speed copper-clad laminates.The phenolic hydroxyl group at the end of PPO plays a key role in its reactivity.Accurately quantifying the phenolic hydroxyl content in PPO is essential but challenging.In this study,we proposed a method for measuring the phenolic hydroxyl content of PPO using differential UV absorption spectroscopy.In alkaline solutions,the phenolic hydroxyl in PPO completely ionizes to form phenoxide ions,leading to a significant increase in UV absorbance at approximately 250 and 300 nm.Notably,the differential UV absorbance at approximately 300 nm was directly proportional to the phenolic hydroxyl concentration.Using 2,6-dimethylphenol as a standard,a calibration curve was established to relate the phenolic hydroxyl concentration to differential UV absorbance at approximately 300 nm,providing a precise and straightforward method for phenolic hydroxyl quantification in PPO with distinct advantages over conventional techniques.
基金financially supported by the International Cooperation Program from the Ministry of Science and Technology of Hubei Province(No.2023EHA069)Shenzhen Science and Technology Program(No.JCYJ20230807143702005)National Foreign Experts Program(No.G2022027015L)。
文摘Magnetic resonance imaging(MRI)is one of the most widely used diagnostic techniques.Iron oxide nanoparticles,as a promising kind of contrast agents,have attracted intense research interest due to their low toxicity and superparamagnetism.However,it is still a great challenge to prepare ideal iron oxide based contrast agents with high uniformity,excellent water solubility and biocompatibility.In this paper,a novel water-soluble polymer ligand pentaerythritol tetrakis 3-mercaptopropionate-poly(N-vinyl-2-pyrrolidone)(PTMP-PVP)was used as a capping reagent to prepare iron oxide nanoparticles MIONs@PTMP-PVP through one-step co-precipitation of iron precursors in aqueous solution at 100℃.The obtained nanoparticles MIONs@PTMP-PVP had a small size and narrow size distribution,and they were found to be biocompatible as determined through CCK-8 assay and histology analysis.In vivo MRI study demonstrated that the obtained MIONs@PTMP-PVP can be potentially used as an effective T_(2)-weighted MRI contrast agent.
基金extend their gratitude to the Deanship of Scientific Research,Vice Presidency for Graduate Studies and Scientific Research,King Faisal University,Saudi Arabia,for funding the publication of this work under the Ambitious Researcher program(Project No.KFU253806).
文摘Artificial intelligence(AI)based models have been used to predict the structural,optical,mechanical,and electrochemical properties of zinc oxide/graphene oxide nanocomposites.Machine learning(ML)models such as Artificial Neural Networks(ANN),Support Vector Regression(SVR),Multilayer Perceptron(MLP),and hybrid,along with fuzzy logic tools,were applied to predict the different properties like wavelength at maximum intensity(444 nm),crystallite size(17.50 nm),and optical bandgap(2.85 eV).While some other properties,such as energy density,power density,and charge transfer resistance,were also predicted with the help of datasets of 1000(80:20).In general,the energy parameters were predicted more accurately by hybrid models.The hydrothermal method was used to synthesize graphene oxide(GO)and zinc oxide(ZnO)nanocomposites.The increased surface area,conductivity,and stability of graphene oxide in zinc oxide nanoparticles make the composite an ideal option for energy storage.X-ray diffraction(XRD)confirmed the crystallite size of 17.41 nm for the nanocomposite and the presence of GO(12.8○)peaks.The scanning electron microscope(SEM)showed anchored wrinkled GO sheets on zinc oxide with an average particle size of 2.93μm.Energy-dispersive X-ray spectroscopy(EDX)confirmed the elemental composition,and Fouriertransform infrared spectroscopy(FTIR)revealed the impact of GO on functional groups and electrochemical behavior.Photoluminescence(PL)wavelength of(439 nm)and band gap of(2.81 eV)show that the material is suitable for energy applications in nanocomposites.Smart nanocomposite materials with improved performance in energy storage and related applications were fabricated by combining synthesis,characterization,fuzzy logic,and machine learning in this work.
基金supported by the National Natural ScienceFoundation of China(Grant No.52203332)。
文摘The thermal decomposition characteristic of ammonium perchlorate(AP)represents a critical factor in determining the performance of solid propellants,which has aroused significant interest on the structure and performance improvement of kinds of catalysts.In this study,bimetallic metal-organic frameworks(MOFs),such as CuCo-BTC(BTC=1,3,5-Benzenetricarboxylic acid,H_(3)BTC),CuNi-BTC,and CoNi-BTC,were synthesized by solvothermal(ST)and spray-drying(SD)methods,and then calcined at 400℃for 2 h to form metal oxides.The catalysts as well as their catalytic effects for AP decomposition were characterized by FTIR,XRD,SEM,XPS,TG,DSC,TG-IR,EIS,CV,and LSV.It was found that the rapid coordination of metal ions with ligands during spray drying may lead to catalytic structural defects,promoting the exposure of reactive active sites and increasing the catalytic active region.The results showed that the addition of 2 wt%binary transition metal oxides(BTMOs)as catalysts significantly reduced the high-temperature decomposition(HTD)temperature of AP and enhanced its heat release.Of particular significance is the observation that SD-CoNiO_(x),prepared by spray-drying,reduced the decomposition temperature of AP from 413.26℃(pure AP)to 306℃and enhanced the heat release from 256.79 J/g(pure AP)to 1496.82 J/g,while concomitantly reducing the activation energy by 42%.By analysing the gaseous products during the decomposition of AP+SD-CoNiO_(x)and AP+ST-CoNiO_(x),it was found that SD-CoNiO_(x)could significantly increase the content of high-valent nitrogen oxides during the AP decomposition reaction,which indicates that the BTMOs prepared by spray-drying in the reaction system are more conducive to accelerating the electron transfer in the thermal decomposition process of AP,and can provide a high concentration of reactive oxygen species that oxidize AP to high-valent nitrogen oxide-containing compounds.The present study shows that the structure selectivity of the spray-drying technique influences surfactant molecular arrangement on catalyst surfaces,resulting in their ability to promote higher electron transfer during the catalytic process.Therefore,BTMOs prepared by spray drying method have higher potential for application.
基金financially supported by the National Natural Science Foundation of China(No.22309067)the Open Project Program of the State Key Laboratory of Materials-Oriented Chemical Engineering,China(No.KL21-05)the Marine Equipment and Technology Institute,Jiangsu University of Science and Technology,China(No.XTCX202404)。
文摘This study focused on improving the cathode performance of Ba_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.15)O_(3-δ)(BSCN)-based perovskite materials through molybdenum(Mo)doping.Pure BSCN and Mo-modified-BSCN—Ea_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.1)Mo_(0.05)O_(3-δ)(B S CNM_(0.05)),Ba_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.05)Mo_(0.1)O_(3-δ)(BSCNM_(0.1)),and Ba_(0.6)Sr_(0.4)Co_(0.85)Mo_(0.15)O_(3-δ)(BSCM)—with Mo doping contents of 5mol%,10mol%,and15mol%,respectively,were successfully prepared using the sol-gel method.The effects of Mo doping on the crystal structure,conductivity,thermal expansion coefficient,oxygen reduction reaction(ORR)activity,and electrochemical performance were systematically evaluated using X-ray diffraction analysis,thermally induced characterization,electrochemical impedance spectroscopy,and single-cell performance tests.The results revealed that Mo doping could improve the conductivity of the materials,suppress their thermal expansion effects,and significantly improve the electrochemical performance.Surface chemical state analysis using X-ray photoelectron spectroscopy revealed that 5mol%Mo doping could facilitate a high adsorbed oxygen concentration leading to enhanced ORR activity in the materials.Density functional theory calculations confirmed that Mo doping promoted the ORR activity in the materials.At an operating temperature of 600℃,the BSCNM_(0.05)cathode material exhibited significantly enhanced electrochemical impedance characteristics,with a reduced area specific resistance of 0.048Ω·cm~2,which was lower than that of the undoped BSCN matrix material by 32.39%.At the same operating temperature,an anode-supported single cell using a BSCNM_(0.05)cathode achieved a peak power density of 1477 mW·cm^(-2),which was 30.71%,56.30%,and 171.50%higher than those of BSCN,BSCNM_(0.1),and B SCM,respectively.The improved ORR activity and electrochemical performance of BSCNM_(0.05)indicate that it can be used as a cathode material in low-temperature solid oxide fuel cells.
基金financial support of the National Natural Science Foundation of China(No.52371103)the Fundamental Research Funds for the Central Universities,China(No.2242023K40028)+1 种基金the Open Research Fund of Jiangsu Key Laboratory for Advanced Metallic Materials,China(No.AMM2023B01).financial support of the Research Fund of Shihezi Key Laboratory of AluminumBased Advanced Materials,China(No.2023PT02)financial support of Guangdong Province Science and Technology Major Project,China(No.2021B0301030005)。
文摘Oxide dispersion strengthened(ODS)alloys are extensively used owing to high thermostability and creep strength contributed from uniformly dispersed fine oxides particles.However,the existence of these strengthening particles also deteriorates the processability and it is of great importance to establish accurate processing maps to guide the thermomechanical processes to enhance the formability.In this study,we performed particle swarm optimization-based back propagation artificial neural network model to predict the high temperature flow behavior of 0.25wt%Al2O3 particle-reinforced Cu alloys,and compared the accuracy with that of derived by Arrhenius-type constitutive model and back propagation artificial neural network model.To train these models,we obtained the raw data by fabricating ODS Cu alloys using the internal oxidation and reduction method,and conducting systematic hot compression tests between 400 and800℃with strain rates of 10^(-2)-10 S^(-1).At last,processing maps for ODS Cu alloys were proposed by combining processing parameters,mechanical behavior,microstructure characterization,and the modeling results achieved a coefficient of determination higher than>99%.
基金supported by the National Key R&D Program of China(Grant Nos.U25A20810 and 2024YFF0508201)the National Natural Science Foundation of China(Grant No.12302504).
文摘In coal mining on a high-pressure Ordovician limestone aquifer,grouting materials should have sufficient mechanical properties,particularly strong interfacial bonding performance to address stress concentration at the grout-limestone interface induced by rock stress disturbances during mining.In this study,graphene oxide(GO)was integrated into cement-polyacrylate composite grout to improve its interfacial bonding.First,four-point bending tests were conducted,and the Monte Carlo method combined with the simplex search algorithm was employed to determine the variations in shear cohesion and static friction parameters.The results reveal that GO can significantly increase both the tensile and shear cohesion of the grout-limestone interface,but minimally affects the interfacial friction coefficient.Second,nuclear magnetic resonance(NMR)and scanning electron microscopy(SEM)tests were performed.The results indicate that GO nanosheets result in a squamaceous microstructure of the grout consolidation mass,increasing the adhesion of the grout-limestone interface.Moreover,spiny Aft(ettringite)clusters can be induced in limestone fracture surfaces by GO,which could serve as anchors for limestone and grout consolidation mass.
基金supported by the National Natural Science Foundation of China(Nos.62104045,52101213)Jiangsu Provincial Department of Science and Technology of China(No.BE2022426).
文摘As the chemical industry expands,the use of benzene,toluene,and xylene(collectively known as BTX)in industrial production has increased greatly.Meanwhile,the toxic nature and potential health hazards of BTX gases cannot be ignored due to low-concentration leaks underline the critical need for rapid and real-time monitoring of these gases.Chemiresistive metal oxide semiconductor(MOS)-based gas sensors,which are extensively used for gas detection in both industrial settings and everyday life,emerge as one of the optimal solutions for trace BTX detection.These sensors are highly valued for their high sensitivity and low detection limits.Nevertheless,the improvement of selectivity towards specific BTX gases to achieve efficient and precise detection still remains challenging.This review summarizes the chemiresistive MOS-based gas sensors designed for BTX detection,categorizing them based on the components of sensing materials-basically into three groups:single-component,single heterojunction,and multiple heterojunctions gas sensing materials.Further,the review proposes the future application prospects of chemiresistive MOS-based BTX gas sensors,with specific emphasis on their significance in promoting industrial safety and environmental monitoring.
