Nowadays, trends in wastewater treatment by zero-valent iron（ZVI） were turned to use bimetallic NZVI particles by planting another metal onto the ZVI surface to increase its reactivity. Nano size zero-valent iron/co...Nowadays, trends in wastewater treatment by zero-valent iron（ZVI） were turned to use bimetallic NZVI particles by planting another metal onto the ZVI surface to increase its reactivity. Nano size zero-valent iron/copper（NZVI/Cu0） bimetallic particles were synthesized in order to examine its toxicity effects on the wastewater microbial life, kinetics of phosphorus, ammonia stripping and the reduction of chemical oxygen demand（COD）.Various concentrations of NZVI/Cu0 and operation conditions both aerobic and anaerobic were investigated and compared with pure NZVI experiment. The results showed that addition10 mg/L of NZVI/Cu0 significantly increased the numbers of bacteria colonies under anaerobic condition, conversely it inhibited bacteria activity with the presence of oxygen. Furthermore,the impact of nanoparticles on ammonia stripping and phosphorus removal was also linked to the emitted iron ions electrons. It was found that dosing high concentration of bimetallic NZVI/Cu0 has a negative effect on ammonia stripping regardless of the aeration condition. In comparison to control, dosing only 10 mg/L NZVI/Cu0, the phosphorus removal increased sharply both under aerobic and anaerobic conditions, these outcomes were obtained as a result of complete dissolution of bimetallic nanoparticles which formed copper-iron oxides components that are attributed to increasing the phosphorus adsorption rate.展开更多
In the present study, pure iron/copper composite metal cladding was deposited onto carbon steel by tungsten inert gas welding. The study focused on interfacial morphological, microstructural, and mechanical analyses o...In the present study, pure iron/copper composite metal cladding was deposited onto carbon steel by tungsten inert gas welding. The study focused on interfacial morphological, microstructural, and mechanical analyses of the composite cladding layers. Iron liquid–solid-phase zones were formed at copper/steel and iron interfaces because of the melting of the steel substrate and iron. Iron concentrated in the copper cladding layer was observed to exhibit belt, globule, and dendrite morphologies. The appearance of iron-rich globules indicated the occurrence of liquid phase separation（LPS） prior to solidification, and iron-rich dendrites crystallized without the occurrence of LPS. The maximum microhardness of the iron/steel interface was lower than that of the copper/steel interface because of the diffusion of elemental carbon. All samples fractured in the cladding layers. Because of a relatively lower strength of the copper layer, a short plateau region appeared when shear movement was from copper to iron.展开更多
This study was conducted in two sections.Initially,the effects of NaCl,MgCl_(2),and urea were investigated on extracting copper and iron from chalcopyrite.Subsequently,CuFe_(2)O_(4)-based electrodes for supercapacitor...This study was conducted in two sections.Initially,the effects of NaCl,MgCl_(2),and urea were investigated on extracting copper and iron from chalcopyrite.Subsequently,CuFe_(2)O_(4)-based electrodes for supercapacitors were synthesized using the extracted solution.The first phase revealed that 3 mol/L NaCl achieved the highest extraction performance,yielding 60%Cu and 23%Fe.MgCl_(2)at 1.5 mol/L extracted 52%Cu and 27%Fe,while a combination of 0.5 mol/L MgCl_(2)and 1.6 mol/L urea yielded 57%Cu and 20%Fe.Urea effectively reduced iron levels.CuFe_(2)O_(4)-based electrodes were then successfully synthesized via a hydrothermal method using a MgCl_(2)-urea solution.Characterization studies confirmed CuFe_(2)O_(4)formation with a 2D structure and 45−50 nm wall thickness on nickel foam.Electrochemical analysis showed a specific capacitance of 725 mF/cm^(2)at 2 mA/cm^(2)current density,with energy and power densities of 12.3 mW·h/cm^(2)and 175 mW/cm^(2),respectively.These findings suggest that chalcopyrite has the potential for direct use in energy storage.展开更多
Copper nanoclusters(CuNCs)have gained prominence due to their remarkable color-tunable light emission and cost-effective,versatile solution-based synthesis.The use of various functional ligands in the synthesis of CuN...Copper nanoclusters(CuNCs)have gained prominence due to their remarkable color-tunable light emission and cost-effective,versatile solution-based synthesis.The use of various functional ligands in the synthesis of CuNCs enables the modulation of their emission wavelengths and enhances their environmental stability.These nanoclusters have found applications across diverse fields,including catalysis,sensing,bioimaging,and optoelectronics.This review offers a focused and up-to-date perspective by covering literature from the past decade(2015―2025)with an explicit emphasis on practical environmental matrices,including heavy metal ions,organic pollutants,pharmaceuticals,and other environmental contaminants.It systematically compares sensing mechanisms(e.g.,fluorescence quenching,turn-on responses,ratiometric and inner-filter effects)and provides tabulated limits of detection for key heavy metals,organic pollutants,and pharmaceuticals to facilitate direct benchmarking.Finally,the review highlights translational gaps for in-field deployment,such as matrix interferences,long-term stability of ligand-stabilized CuNCs,sample pre-treatment needs,and the absence of standardized validation protocols and proposes targeted research directions to bridge laboratory advances with real-world environmental monitoring.展开更多
Copper materials have emerged as the preferred choice for marine heat exchangers owing to their excep-tional thermal conductivity.The enhancement of surface performance can be significantly achieved by engineering mic...Copper materials have emerged as the preferred choice for marine heat exchangers owing to their excep-tional thermal conductivity.The enhancement of surface performance can be significantly achieved by engineering micro-nano structures on the material’s surface,thereby attaining improved corrosion resis-tance and antibacterial properties in complex marine environments.In this study,we directly fabricated a copper nanopillar array structure on the substrate via template-assisted electrodeposition.Subsequently,passivation of the pillar-structured copper surface was achieved through a formate&dodecanethiol-assisted solvothermal process(Cu/FA-DT).The results indicate that the nanopillar structure effectively eliminates bacteria through physical rupture upon contact,leading to an 85.47%reduction in P.aerug-inosa adhesion compared to untreated samples after 72 h of immersion in seawater.Furthermore,cor-rosion resistance is significantly enhanced,with inhibition rates of approximately 95.27%and 90.50%in natural and P.aeruginosa containing seawater,respectively.Notably,the thermal conductivity of copper is well preserved,ensuring its functional integrity in marine heat exchange environments.After 7 days of immersion in natural and P.aeruginosa containing seawater,the thermal conductivity of Cu/FA-DT de-creased by only 15.41%and 2.78%,respectively,demonstrating superior thermal conductivity retention compared to untreated bare copper.This study provides valuable insights into the potential application of traditional copper in marine heat exchange environments.展开更多
Copper complexes inspired by O_(2)-activating enzymes have been widely investigated as molecular water oxidation catalysts,capable of facile and reversible O─O bond formation and cleavage under mild conditions.In thi...Copper complexes inspired by O_(2)-activating enzymes have been widely investigated as molecular water oxidation catalysts,capable of facile and reversible O─O bond formation and cleavage under mild conditions.In this study,two copper phenanthroline complexes,namely,Cu(phen)and Cu(dophen),exhibit high turnover frequencies(TOFs)of 74±13 and(5.66±0.29)×10^(3)s^(−1)for water oxidation,respectively.Moreover,amino acid-functionalized carbon dots(CDs)were used to support the adhesion of the[Cu]complexes onto the electrode,significantly enhancing the TOFs of(2.80±0.12)×10^(3)and(4.11±0.24)×10^(4)s^(−1),respectively,exceeding the activity of photosystem Ⅱ in nature.Remarkably,the amino acid-functionalized CDs provide a secondary sphere that mimics the catalytic microenvironment of the copper centre,which promotes proton-coupled electron transfer and O─O bond formation.Finally,the photovoltaic-electrolysis(PVE)system was established using CDs-supported Cu catalysts and commercial silicon solar panels,achieving a high solar-to-hydrogen efficiency of 11.59%under the illumination of AM 1.5 G.This represents the most efficient solar-driven water splitting system based on copper-based catalysts to date,introducing the biomimetic secondary sphere to a“proton-rocking”process for water oxidation catalysis and application of the PVE system.展开更多
The present work provides a facile and efficient method for producing ultrafine copper powders.Ultrafine copper powders were synthesized through a solvothermal method,utilizing ethanol both as a solvent and a reducing...The present work provides a facile and efficient method for producing ultrafine copper powders.Ultrafine copper powders were synthesized through a solvothermal method,utilizing ethanol both as a solvent and a reducing agent.Specifically,by exploiting the weak reducing property of ethanol,the copper precursor is first converted to copper oxide and then further reduced to cuprous oxide and pure copper.Such a method can effectively control the morphology and particle size of the copper powder,reduce particle aggregation,and enhance oxidation resistance.It is cost-effective and produces fewer toxic by-products.Spherical copper particles with an average particle size of about 180 nm were obtained.The initial oxidation temperature is approximately 150℃,and the resulting copper powders can be stored stably under ambient conditions for at least 5 months,demonstrating excellent oxidation resistance and thermal stability.展开更多
The corrosion resistance of aluminum(Al)cable-copper(Cu)terminal joints fabricated by magnetic pulse crimping(MPC)and hydraulic clamp crimping(HCC)was compared.Performance degradation was evaluated by mechanical and e...The corrosion resistance of aluminum(Al)cable-copper(Cu)terminal joints fabricated by magnetic pulse crimping(MPC)and hydraulic clamp crimping(HCC)was compared.Performance degradation was evaluated by mechanical and electrical properties.Additionally,corrosion behavior was analyzed by electrochemical testing.Microscopic characterization was performed by scanning electron microscopy(SEM)and energy dispersive spectroscopy(EDS).Results show that the tensile strength of the corroded joints is reduced.However,due to the advantages of high-speed forming and contact tightness unique to MPC,the contact resistance of the corroded joints still maintains excellent.Electrochemical tests demonstrate that the MPC joints have higher corrosion potentials and smaller corrosion currents,providing better corrosion resistance.The formation of a primary battery between Al and Cu at the lap joint leads to the formation of severer corrosion pits.展开更多
This paper reports the preparation of three di‑iron complexes containing a thiazole moiety.Esterification of complex[Fe_(2)(CO)_(6)(μ‑SCH_(2)CH(CH_(2)OH)S)](1)with 4‑methylthiazole‑5‑carboxylic acid gave the correspo...This paper reports the preparation of three di‑iron complexes containing a thiazole moiety.Esterification of complex[Fe_(2)(CO)_(6)(μ‑SCH_(2)CH(CH_(2)OH)S)](1)with 4‑methylthiazole‑5‑carboxylic acid gave the corresponding ester[Fe_(2)(CO)_(6)(μ‑tedt)](2),where tedt=SCH_(2)CH(CH_(2)OOC(5‑C_(3)HNSCH_(3)))S.Further reactions of complex 2 with tri(ptolyl)phosphine(tp)or tris(4‑fluorophenyl)phosphine(fp)gave the phosphine‑substituted derivatives[Fe_(2)(CO)_(5)(tp)(μ‑tedt)](3)and[Fe_(2)(CO)_(5)(fp)(μ‑tedt)](4).The structures of the newly prepared complexes were elucidated by elemental analysis,NMR,IR,and X‑ray photoelectron spectroscopy.Moreover,single‑crystal X‑ray diffraction analysis confirmed their molecular structures,showing that they contain a di‑iron core ligated by a bridged dithiolate bearing a thiazole moiety and terminal carbonyls.The electrochemical and electrocatalytic proton reduction were probed by cyclic voltammetry,revealing that three complexes can catalyze the reduction of protons to H_(2) under the electrochemical conditions.For comparison,complex 4 possessed the best efficiency with a turnover frequency of 23.5 s^(-1)at 10 mmol·L^(-1)HOAc concentration.In addition,the fungicidal activity of these complexes was also investigated in this study.CCDC:2477511,2;2477512,3;2477513,4.展开更多
Neurodegenerative diseases are prevalent conditions that greatly impact human health.These diseases are primarily characterized by the progressive loss and eventual death of neuronal function,although the precise mech...Neurodegenerative diseases are prevalent conditions that greatly impact human health.These diseases are primarily characterized by the progressive loss and eventual death of neuronal function,although the precise mechanisms underlying these processes remain incompletely understood.Iron is an essential trace element in the human body,playing a crucial role in various biological processes.The maintenance of iron homeostasis relies on the body's intricate and nuanced regulatory mechanisms.In recent years,considerable attention has been directed toward the relationship between dysregulated iron homeostasis and neurodegenerative diseases.The regulation of iron homeostasis within cells is crucial for maintaining proper nervous system function.Research has already revealed that disruptions in iron homeostasis may lead to ferroptosis and oxidative stress,which,in turn,can impact neuronal health and contribute to the development of neurodegenerative diseases.This article primarily explores the intimate relationship between iron homeostasis and neurodegenerative diseases,aiming to provide novel insights and strategies for treating these debilitating conditions.展开更多
Iron deficiency anemia affects approximately 1.62 billion people worldwide,yet traditional iron supplements present bioavailability limitations and gastrointestinal side effects.This randomized,double-blind clinical t...Iron deficiency anemia affects approximately 1.62 billion people worldwide,yet traditional iron supplements present bioavailability limitations and gastrointestinal side effects.This randomized,double-blind clinical trial investigated a novel Auricularia auricula polysaccharide-iron complex(AAPIC)compared with heme iron and ferrous glycinate in 180 iron-deficient adults receiving 30 mg elemental iron daily for 12 weeks.AAPIC achieved comparable hemoglobin improvements(from 98.3±8.7 to 126.5±9.2 g/L)to heme iron(from 97.8±9.1 to 128.3±8.6 g/L)and was significantly superior to ferrous glycinate(from 98.6±8.9 to 119.7±10.3 g/L;p<0.001).Iron absorption efficiency showed AAPIC at 23.7±4.2%,heme iron at 25.1±3.8%,and ferrous glycinate at 18.4±5.1%.Toxicological assessments revealed no hepatotoxicity,nephrotoxicity,or mutagenicity.Gastrointestinal adverse events occurred in 8.3%of AAPIC recipients versus 15.0%with ferrous glycinate and 10.0%with heme iron.The polysaccharide component facilitates iron transport through enhanced intestinal uptake mechanisms.AAPIC represents a promising,well-tolerated alternative with clinical efficacy comparable to established iron formulations.展开更多
The combination of electrochemistry and metal catalysts has been a popular research topic in the field of organic synthesis due to the abundance and controllable valence states of transition metals,where electron tran...The combination of electrochemistry and metal catalysts has been a popular research topic in the field of organic synthesis due to the abundance and controllable valence states of transition metals,where electron transfer at the electrode produces catalysts with more valence states.Among these transition metal catalysts,electrochemical conversions catalyzed by inexpensive copper metals have received considerable attention.This article systematically investigated this field and reviewed the electrochemical copper catalytic methods applied in organic synthesis from the different activation modes of substrates,which can be broadly classified into the functionalization of C=C bonds,C-H bond activation,C-C and C-X bond activation,and so on.展开更多
In this study,copper extraction from low-grade oxide-sulfide ores was investigated using a leaching method combined with response surface methodology(RSM)to optimize operational conditions and assess leaching kinetics...In this study,copper extraction from low-grade oxide-sulfide ores was investigated using a leaching method combined with response surface methodology(RSM)to optimize operational conditions and assess leaching kinetics.Given copper's extensive industrial applications,sustainable recovery from low-grade ores is critical.Five key parameters-acid concentration,leaching time,particle size,temperature,and solids percentage-were identified as major influences on copper recovery.The results revealed that leaching time and solids percentage,along with interactions between temperature-time and temperature-solids percentage,had the most significant effects.Optimal conditions for 80% copper recovery while minimizing iron recovery below 3% included an acid concentration of 1.21 mol L^(-1),a leaching time of 108 min,a particle size of 438μm,a temperature of 45℃,and a solids percentage of 18.2%.Leaching kinetics were analyzed using shrinking core models,with the Dickinson model best describing the process,showing an activation energy of 32.63 kJ mol^(-1),indicative of mixed diffusion and chemical reaction control.The final kinetic model effectively predicted the influence of key parameters.These findings highlight the importance of optimizing process variables and selecting suitable kinetic models to enhance extraction efficiency,reduce costs,and improve sustainability in copper recovery.展开更多
A series of leaching and electrochemical experiments were conducted to elucidate the critical role of hydrogen sulfide(H_(2)S)in copper-driven reduction of chalcopyrite.Results demonstrate that in the absence of H_(2)...A series of leaching and electrochemical experiments were conducted to elucidate the critical role of hydrogen sulfide(H_(2)S)in copper-driven reduction of chalcopyrite.Results demonstrate that in the absence of H_(2)S,metallic copper converts chalcopyrite into bornite(Cu_(5)FeS_(4)).However,the introduction of H_(2)S promotes the formation of chalcocite(Cu_(2)S)by altering the oxidation pathway of copper.Electrochemical analysis demonstrates that the presence of H₂S significantly reduces the corrosion potential of copper from 0.251 to−0.223 V(vs SHE),reaching the threshold necessary for the formation of Cu_(2)S.Nevertheless,excessive H_(2)S triggers sulfate reduction via the reaction of 8Cu+H_(2)SO_(4)+3H_(2)S=4Cu_(2)S+4H_(2)O(ΔG=−519.429 kJ/mol at 50℃),leading to inefficient copper utilization.展开更多
Copper ions are essential for cellular function but can induce cytotoxic effects when dysregulated.This review explores the multifaceted role of copper in cancer metabolism with a focus on the novel concept of cupropt...Copper ions are essential for cellular function but can induce cytotoxic effects when dysregulated.This review explores the multifaceted role of copper in cancer metabolism with a focus on the novel concept of cuproptosis,a regulated form of cell death triggered by copper accumulation.The mechanisms underlying copper homeostasis are detailed,including dietary absorption,systemic distribution,and intracellular utilization.Key transporters,such as copper transporter 1(CTR1)and ATPase copper transporting alpha/b(ATP7A/B),are highlighted.Cancer cells often exhibit elevated copper levels,supporting proliferation and metastasis through pro-tumorigenic pathways.Recent studies have shown that disrupting copper homeostasis can induce cuproptosis,which is characterized by the aggregation of lipoylated mitochondrial proteins and disruption of iron-sulfur cluster biogenesis.Advances in copper-based nanotechnology have enabled targeted delivery of copper to tumors,enhancing therapeutic efficacy through synergistic effects with reactive oxygen species(ROS)generation and immunomodulation.However,the hypoxic tumor microenvironment poses significant challenges by upregulating copper-sequestering proteins and downregulating key cuproptosis mediators.Future directions include integrating multi-omics approaches to identify novel therapeutic targets and developing combination therapies to overcome hypoxia-induced resistance.This review provides a comprehensive overview of copper metabolism in cancer,emphasizing the potential of cuproptosis induction as a powerful strategy for oncologic intervention.展开更多
The formation of copper deposits is closely related to hydrothermal processes.Understanding the migration of copper in hydrothermal fluids aids in reconstructing mineralization processes and deciphering deposit genesi...The formation of copper deposits is closely related to hydrothermal processes.Understanding the migration of copper in hydrothermal fluids aids in reconstructing mineralization processes and deciphering deposit genesis.Copper primarily exists as Cu^(+)and Cu^(2+)in hydrothermal solutions,with redox conditions governing their interconversion.In chloride-rich geological fluids,Cu-Cl complexes are considered critical for copper transport.However,the specific types and valence transitions of Cu-Cl complexes under varying hydrothermal conditions remain poorly understood.This study employed in situ Raman spectroscopy to systematically analyze Cu+HCl and CuCl_(2)+K_(2)S_(2)O_(3)/H_(2) systems under saturated vapor pressure at 25-300℃,elucidating the effects of temperature,Cl^(-)concentration,and redox conditions on copper speciation.In the Cu^(+)HCl system,copper dissolved as monovalent Cu-Cl complexes.At high temperatures(>200℃),[CuCl_(2)]^(-)is the dominated species,whereas[CuCl_(3)]^(2-)becomes prevalent at lower temperatures and higher HCl concentrations.For the Cu^(2+)-Cl system,the dominant species transitioned from[Cu(H_(2)O)n]^(2+)(<50℃)to[CuCl_(4)]^(2-)(100℃)and further to[CuCl]^(+)and[CuCl_(2)]^(0) at 300℃.The introduction of reducing agents(K_(2)S_(2)O_(3)/H_(2))facilitated Cu^(2+)→Cu^(+)reduction,thereby stabilizing Cu^(+)-Cl complexes and inducing partial copper precipitation.The behavior of copper in chloriderich hydrothermal fluids observed in this study indicates that high-temperature oxidizing fluids facilitate Cu mobilization,while cooling and redox changes promote deposition and ore minerals formation.展开更多
At 82,master craftsman Zhu Bingren,China’s preeminent copper artist,continues to dynamically evolve his ancient heritage,proving that true preservation lies in innovation and bringing tradition into the contemporary ...At 82,master craftsman Zhu Bingren,China’s preeminent copper artist,continues to dynamically evolve his ancient heritage,proving that true preservation lies in innovation and bringing tradition into the contemporary world.THE copper art should not be confined to display cases,believes artist Zhu Bingren.From living rooms to fashion runways,and from the Great Wall in Beijing to the Louvre in Paris,the Chinese master craftsman brings his metal creations to life in diverse settings.展开更多
It is difficult to recover chrysocolla from sulfidation flotation which is closely related to the mineral surface composition.In this study,the effects of fluoride roasting on the surface composition of chrysocolla we...It is difficult to recover chrysocolla from sulfidation flotation which is closely related to the mineral surface composition.In this study,the effects of fluoride roasting on the surface composition of chrysocolla were investigated,its impact on sulfidation flotation was explored,and the mechanisms involved in both fluoride roasting and sulfidation flotation were discussed.With CaF_(2)as the roasting reagent,Na_(2)S·9H_(2)O as the sulfidation reagent,and sodium butyl xanthate(NaBX)as the collector,the results of the flotation experiments showed that fluoride roasting improved the floatability of chrysocolla,and the recovery rate increased from 16.87%to 82.74%.X-ray diffraction analysis revealed that after fluoride roasting,approximately all the Cu on the chrysocolla surface was exposed in the form of CuO,which could provide a basis for subsequent sulfidation flotation.The microscopy and elemental analyses revealed that large quantities of"pagoda-like"grains were observed on the sulfidation surface of the fluoride-roasted chrysocolla,indicating high crystallinity particles of copper sulfide.This suggests that the effect of sulfide formation on the chrysocolla surface was more pronounced.X-ray photoelectron spectroscopy revealed that fluoride roasting increased the relative contents of sulfur and copper on the surface and that both the Cu~+and polysulfide fractions on the surface of the minerals increased.This enhances the effect of sulfidation,which is conducive to flotation recovery.Therefore,fluoride roasting improved the effect of copper species transformation and sulfidation on the surface of chysocolla,promoted the adsorption of collectors,and improved the recovery of chrysocolla from sulfidation flotation.展开更多
Centrifugal casting of ductile iron pipe is a high-temperature,semi-continuous production process.However,conducting laboratory research on the solidification process of centrifugal casting of ductile iron pipe presen...Centrifugal casting of ductile iron pipe is a high-temperature,semi-continuous production process.However,conducting laboratory research on the solidification process of centrifugal casting of ductile iron pipe presents significant challenges.In this study,a novel research method was introduced for investigating the solidification process of ductile iron pipe,namely thermal simulation of ductile iron pipe.Comparative research was conducted on the microstructure and properties of the thermal simulation sample and the ductile iron pipe.The findings indicate that the thermal simulation sample and ductile iron pipe exhibit good heat transfer similarity and microstructure similarity.The difference of cooling rate between thermal simulation sample and ductile pipe is less than 0.24℃·s^(-1),and the difference of microstructure content of free cementite,ferrite,and pearlite is less than 5%.The tensile strength of annealed ductile iron pipe is 466 MPa,with an elongation of 16.1%and a Brinell hardness of 156.5 HBW.In comparison,the tensile strength of annealed thermal simulation sample is 482.0 MPa,with an elongation of 15.5%and a Brinell hardness of 159.0 HBW.These results suggest that the thermal simulation experimental research method is both scientific and feasible,offering an objective,reliable,and cost-effective approach to laboratory research on ductile iron pipe.展开更多
基金supported by Kyushu University,Japan and the Japanese Ministry of Education,Culture,Sports,Science,and Technology(MEXT)
文摘Nowadays, trends in wastewater treatment by zero-valent iron（ZVI） were turned to use bimetallic NZVI particles by planting another metal onto the ZVI surface to increase its reactivity. Nano size zero-valent iron/copper（NZVI/Cu0） bimetallic particles were synthesized in order to examine its toxicity effects on the wastewater microbial life, kinetics of phosphorus, ammonia stripping and the reduction of chemical oxygen demand（COD）.Various concentrations of NZVI/Cu0 and operation conditions both aerobic and anaerobic were investigated and compared with pure NZVI experiment. The results showed that addition10 mg/L of NZVI/Cu0 significantly increased the numbers of bacteria colonies under anaerobic condition, conversely it inhibited bacteria activity with the presence of oxygen. Furthermore,the impact of nanoparticles on ammonia stripping and phosphorus removal was also linked to the emitted iron ions electrons. It was found that dosing high concentration of bimetallic NZVI/Cu0 has a negative effect on ammonia stripping regardless of the aeration condition. In comparison to control, dosing only 10 mg/L NZVI/Cu0, the phosphorus removal increased sharply both under aerobic and anaerobic conditions, these outcomes were obtained as a result of complete dissolution of bimetallic nanoparticles which formed copper-iron oxides components that are attributed to increasing the phosphorus adsorption rate.
基金financially supported by the National Natural Science Foundation of China (No. 51575132)
文摘In the present study, pure iron/copper composite metal cladding was deposited onto carbon steel by tungsten inert gas welding. The study focused on interfacial morphological, microstructural, and mechanical analyses of the composite cladding layers. Iron liquid–solid-phase zones were formed at copper/steel and iron interfaces because of the melting of the steel substrate and iron. Iron concentrated in the copper cladding layer was observed to exhibit belt, globule, and dendrite morphologies. The appearance of iron-rich globules indicated the occurrence of liquid phase separation（LPS） prior to solidification, and iron-rich dendrites crystallized without the occurrence of LPS. The maximum microhardness of the iron/steel interface was lower than that of the copper/steel interface because of the diffusion of elemental carbon. All samples fractured in the cladding layers. Because of a relatively lower strength of the copper layer, a short plateau region appeared when shear movement was from copper to iron.
文摘This study was conducted in two sections.Initially,the effects of NaCl,MgCl_(2),and urea were investigated on extracting copper and iron from chalcopyrite.Subsequently,CuFe_(2)O_(4)-based electrodes for supercapacitors were synthesized using the extracted solution.The first phase revealed that 3 mol/L NaCl achieved the highest extraction performance,yielding 60%Cu and 23%Fe.MgCl_(2)at 1.5 mol/L extracted 52%Cu and 27%Fe,while a combination of 0.5 mol/L MgCl_(2)and 1.6 mol/L urea yielded 57%Cu and 20%Fe.Urea effectively reduced iron levels.CuFe_(2)O_(4)-based electrodes were then successfully synthesized via a hydrothermal method using a MgCl_(2)-urea solution.Characterization studies confirmed CuFe_(2)O_(4)formation with a 2D structure and 45−50 nm wall thickness on nickel foam.Electrochemical analysis showed a specific capacitance of 725 mF/cm^(2)at 2 mA/cm^(2)current density,with energy and power densities of 12.3 mW·h/cm^(2)and 175 mW/cm^(2),respectively.These findings suggest that chalcopyrite has the potential for direct use in energy storage.
文摘Copper nanoclusters(CuNCs)have gained prominence due to their remarkable color-tunable light emission and cost-effective,versatile solution-based synthesis.The use of various functional ligands in the synthesis of CuNCs enables the modulation of their emission wavelengths and enhances their environmental stability.These nanoclusters have found applications across diverse fields,including catalysis,sensing,bioimaging,and optoelectronics.This review offers a focused and up-to-date perspective by covering literature from the past decade(2015―2025)with an explicit emphasis on practical environmental matrices,including heavy metal ions,organic pollutants,pharmaceuticals,and other environmental contaminants.It systematically compares sensing mechanisms(e.g.,fluorescence quenching,turn-on responses,ratiometric and inner-filter effects)and provides tabulated limits of detection for key heavy metals,organic pollutants,and pharmaceuticals to facilitate direct benchmarking.Finally,the review highlights translational gaps for in-field deployment,such as matrix interferences,long-term stability of ligand-stabilized CuNCs,sample pre-treatment needs,and the absence of standardized validation protocols and proposes targeted research directions to bridge laboratory advances with real-world environmental monitoring.
基金financially supported by the National Natural Science Foundation of China(Nos.42276212,42176043,and U2106206)the Shandong University Future Plan for Young Scholars.We thank Sen Wang,Haiyan Yu,and Xiaomin Zhao from the State Key Laboratory of Microbial Technology,Shandong University for the assistance in the microimaging of SEM analysis.
文摘Copper materials have emerged as the preferred choice for marine heat exchangers owing to their excep-tional thermal conductivity.The enhancement of surface performance can be significantly achieved by engineering micro-nano structures on the material’s surface,thereby attaining improved corrosion resis-tance and antibacterial properties in complex marine environments.In this study,we directly fabricated a copper nanopillar array structure on the substrate via template-assisted electrodeposition.Subsequently,passivation of the pillar-structured copper surface was achieved through a formate&dodecanethiol-assisted solvothermal process(Cu/FA-DT).The results indicate that the nanopillar structure effectively eliminates bacteria through physical rupture upon contact,leading to an 85.47%reduction in P.aerug-inosa adhesion compared to untreated samples after 72 h of immersion in seawater.Furthermore,cor-rosion resistance is significantly enhanced,with inhibition rates of approximately 95.27%and 90.50%in natural and P.aeruginosa containing seawater,respectively.Notably,the thermal conductivity of copper is well preserved,ensuring its functional integrity in marine heat exchange environments.After 7 days of immersion in natural and P.aeruginosa containing seawater,the thermal conductivity of Cu/FA-DT de-creased by only 15.41%and 2.78%,respectively,demonstrating superior thermal conductivity retention compared to untreated bare copper.This study provides valuable insights into the potential application of traditional copper in marine heat exchange environments.
基金supported by the National Natural Science Foundation of China(No.52273187)National Key R&D Program of China(2021YFA1500800)+1 种基金Guangdong Basic and Applied Basic Research Foundation(2022A1515110372,2023A1515011306,2023A1515240077)Guangdong-Hong Kong Joint Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province(2023B1212120011)。
文摘Copper complexes inspired by O_(2)-activating enzymes have been widely investigated as molecular water oxidation catalysts,capable of facile and reversible O─O bond formation and cleavage under mild conditions.In this study,two copper phenanthroline complexes,namely,Cu(phen)and Cu(dophen),exhibit high turnover frequencies(TOFs)of 74±13 and(5.66±0.29)×10^(3)s^(−1)for water oxidation,respectively.Moreover,amino acid-functionalized carbon dots(CDs)were used to support the adhesion of the[Cu]complexes onto the electrode,significantly enhancing the TOFs of(2.80±0.12)×10^(3)and(4.11±0.24)×10^(4)s^(−1),respectively,exceeding the activity of photosystem Ⅱ in nature.Remarkably,the amino acid-functionalized CDs provide a secondary sphere that mimics the catalytic microenvironment of the copper centre,which promotes proton-coupled electron transfer and O─O bond formation.Finally,the photovoltaic-electrolysis(PVE)system was established using CDs-supported Cu catalysts and commercial silicon solar panels,achieving a high solar-to-hydrogen efficiency of 11.59%under the illumination of AM 1.5 G.This represents the most efficient solar-driven water splitting system based on copper-based catalysts to date,introducing the biomimetic secondary sphere to a“proton-rocking”process for water oxidation catalysis and application of the PVE system.
文摘The present work provides a facile and efficient method for producing ultrafine copper powders.Ultrafine copper powders were synthesized through a solvothermal method,utilizing ethanol both as a solvent and a reducing agent.Specifically,by exploiting the weak reducing property of ethanol,the copper precursor is first converted to copper oxide and then further reduced to cuprous oxide and pure copper.Such a method can effectively control the morphology and particle size of the copper powder,reduce particle aggregation,and enhance oxidation resistance.It is cost-effective and produces fewer toxic by-products.Spherical copper particles with an average particle size of about 180 nm were obtained.The initial oxidation temperature is approximately 150℃,and the resulting copper powders can be stored stably under ambient conditions for at least 5 months,demonstrating excellent oxidation resistance and thermal stability.
基金supported by the National Natural Science Foundation of China (No.52175315)the Shenzhen Science and Technology Program,China (No.KQTD20200820113110016)the Hunan Provincial Postgraduate Research Innovation Program,China (No.CX20220404)。
文摘The corrosion resistance of aluminum(Al)cable-copper(Cu)terminal joints fabricated by magnetic pulse crimping(MPC)and hydraulic clamp crimping(HCC)was compared.Performance degradation was evaluated by mechanical and electrical properties.Additionally,corrosion behavior was analyzed by electrochemical testing.Microscopic characterization was performed by scanning electron microscopy(SEM)and energy dispersive spectroscopy(EDS).Results show that the tensile strength of the corroded joints is reduced.However,due to the advantages of high-speed forming and contact tightness unique to MPC,the contact resistance of the corroded joints still maintains excellent.Electrochemical tests demonstrate that the MPC joints have higher corrosion potentials and smaller corrosion currents,providing better corrosion resistance.The formation of a primary battery between Al and Cu at the lap joint leads to the formation of severer corrosion pits.
文摘This paper reports the preparation of three di‑iron complexes containing a thiazole moiety.Esterification of complex[Fe_(2)(CO)_(6)(μ‑SCH_(2)CH(CH_(2)OH)S)](1)with 4‑methylthiazole‑5‑carboxylic acid gave the corresponding ester[Fe_(2)(CO)_(6)(μ‑tedt)](2),where tedt=SCH_(2)CH(CH_(2)OOC(5‑C_(3)HNSCH_(3)))S.Further reactions of complex 2 with tri(ptolyl)phosphine(tp)or tris(4‑fluorophenyl)phosphine(fp)gave the phosphine‑substituted derivatives[Fe_(2)(CO)_(5)(tp)(μ‑tedt)](3)and[Fe_(2)(CO)_(5)(fp)(μ‑tedt)](4).The structures of the newly prepared complexes were elucidated by elemental analysis,NMR,IR,and X‑ray photoelectron spectroscopy.Moreover,single‑crystal X‑ray diffraction analysis confirmed their molecular structures,showing that they contain a di‑iron core ligated by a bridged dithiolate bearing a thiazole moiety and terminal carbonyls.The electrochemical and electrocatalytic proton reduction were probed by cyclic voltammetry,revealing that three complexes can catalyze the reduction of protons to H_(2) under the electrochemical conditions.For comparison,complex 4 possessed the best efficiency with a turnover frequency of 23.5 s^(-1)at 10 mmol·L^(-1)HOAc concentration.In addition,the fungicidal activity of these complexes was also investigated in this study.CCDC:2477511,2;2477512,3;2477513,4.
基金supported in part by the National Natural Science Foundation of China,No.82371153(to YS)the Natural Science Foundation of Shandong Province,Nos.ZR2021MH378,ZR2022QH073(to LC)+1 种基金the Shandong Society of Geriatric Science and Technology Project,No.LKJGG2021Z020(to YS)the Yantai Science and Technology Innovation Development Project,Nos.2022YD009,2023YD050。
文摘Neurodegenerative diseases are prevalent conditions that greatly impact human health.These diseases are primarily characterized by the progressive loss and eventual death of neuronal function,although the precise mechanisms underlying these processes remain incompletely understood.Iron is an essential trace element in the human body,playing a crucial role in various biological processes.The maintenance of iron homeostasis relies on the body's intricate and nuanced regulatory mechanisms.In recent years,considerable attention has been directed toward the relationship between dysregulated iron homeostasis and neurodegenerative diseases.The regulation of iron homeostasis within cells is crucial for maintaining proper nervous system function.Research has already revealed that disruptions in iron homeostasis may lead to ferroptosis and oxidative stress,which,in turn,can impact neuronal health and contribute to the development of neurodegenerative diseases.This article primarily explores the intimate relationship between iron homeostasis and neurodegenerative diseases,aiming to provide novel insights and strategies for treating these debilitating conditions.
文摘Iron deficiency anemia affects approximately 1.62 billion people worldwide,yet traditional iron supplements present bioavailability limitations and gastrointestinal side effects.This randomized,double-blind clinical trial investigated a novel Auricularia auricula polysaccharide-iron complex(AAPIC)compared with heme iron and ferrous glycinate in 180 iron-deficient adults receiving 30 mg elemental iron daily for 12 weeks.AAPIC achieved comparable hemoglobin improvements(from 98.3±8.7 to 126.5±9.2 g/L)to heme iron(from 97.8±9.1 to 128.3±8.6 g/L)and was significantly superior to ferrous glycinate(from 98.6±8.9 to 119.7±10.3 g/L;p<0.001).Iron absorption efficiency showed AAPIC at 23.7±4.2%,heme iron at 25.1±3.8%,and ferrous glycinate at 18.4±5.1%.Toxicological assessments revealed no hepatotoxicity,nephrotoxicity,or mutagenicity.Gastrointestinal adverse events occurred in 8.3%of AAPIC recipients versus 15.0%with ferrous glycinate and 10.0%with heme iron.The polysaccharide component facilitates iron transport through enhanced intestinal uptake mechanisms.AAPIC represents a promising,well-tolerated alternative with clinical efficacy comparable to established iron formulations.
基金supported by the National Natural Science Foundation of China (No.22271166)the Frontiers Science Center for New Organic Matter,Nankai University (No.63181206) for generous financial support for our programs。
文摘The combination of electrochemistry and metal catalysts has been a popular research topic in the field of organic synthesis due to the abundance and controllable valence states of transition metals,where electron transfer at the electrode produces catalysts with more valence states.Among these transition metal catalysts,electrochemical conversions catalyzed by inexpensive copper metals have received considerable attention.This article systematically investigated this field and reviewed the electrochemical copper catalytic methods applied in organic synthesis from the different activation modes of substrates,which can be broadly classified into the functionalization of C=C bonds,C-H bond activation,C-C and C-X bond activation,and so on.
基金Open Access funding enabled and organized by Projekt DEAL.
文摘In this study,copper extraction from low-grade oxide-sulfide ores was investigated using a leaching method combined with response surface methodology(RSM)to optimize operational conditions and assess leaching kinetics.Given copper's extensive industrial applications,sustainable recovery from low-grade ores is critical.Five key parameters-acid concentration,leaching time,particle size,temperature,and solids percentage-were identified as major influences on copper recovery.The results revealed that leaching time and solids percentage,along with interactions between temperature-time and temperature-solids percentage,had the most significant effects.Optimal conditions for 80% copper recovery while minimizing iron recovery below 3% included an acid concentration of 1.21 mol L^(-1),a leaching time of 108 min,a particle size of 438μm,a temperature of 45℃,and a solids percentage of 18.2%.Leaching kinetics were analyzed using shrinking core models,with the Dickinson model best describing the process,showing an activation energy of 32.63 kJ mol^(-1),indicative of mixed diffusion and chemical reaction control.The final kinetic model effectively predicted the influence of key parameters.These findings highlight the importance of optimizing process variables and selecting suitable kinetic models to enhance extraction efficiency,reduce costs,and improve sustainability in copper recovery.
基金financially supported by the National Key Research and Development Program of China (No. 2022YFC2105300)。
文摘A series of leaching and electrochemical experiments were conducted to elucidate the critical role of hydrogen sulfide(H_(2)S)in copper-driven reduction of chalcopyrite.Results demonstrate that in the absence of H_(2)S,metallic copper converts chalcopyrite into bornite(Cu_(5)FeS_(4)).However,the introduction of H_(2)S promotes the formation of chalcocite(Cu_(2)S)by altering the oxidation pathway of copper.Electrochemical analysis demonstrates that the presence of H₂S significantly reduces the corrosion potential of copper from 0.251 to−0.223 V(vs SHE),reaching the threshold necessary for the formation of Cu_(2)S.Nevertheless,excessive H_(2)S triggers sulfate reduction via the reaction of 8Cu+H_(2)SO_(4)+3H_(2)S=4Cu_(2)S+4H_(2)O(ΔG=−519.429 kJ/mol at 50℃),leading to inefficient copper utilization.
基金supported by the National Natural Science Foundation of China(Grant Nos.82303206,82372749,and 82072951)Science and Technology Commission of Shanghai Municipality(Grant Nos.20Y11914300 and 22Y21900100)+2 种基金Shanghai Anticancer Association(Grant No.SACAAX202213)Major Research Projects of Taizhou Clinical Medical College(Grant No.TZKY20230308)Natural Science Foundation in University of Jiangsu Province(Grant No.BK20231261).
文摘Copper ions are essential for cellular function but can induce cytotoxic effects when dysregulated.This review explores the multifaceted role of copper in cancer metabolism with a focus on the novel concept of cuproptosis,a regulated form of cell death triggered by copper accumulation.The mechanisms underlying copper homeostasis are detailed,including dietary absorption,systemic distribution,and intracellular utilization.Key transporters,such as copper transporter 1(CTR1)and ATPase copper transporting alpha/b(ATP7A/B),are highlighted.Cancer cells often exhibit elevated copper levels,supporting proliferation and metastasis through pro-tumorigenic pathways.Recent studies have shown that disrupting copper homeostasis can induce cuproptosis,which is characterized by the aggregation of lipoylated mitochondrial proteins and disruption of iron-sulfur cluster biogenesis.Advances in copper-based nanotechnology have enabled targeted delivery of copper to tumors,enhancing therapeutic efficacy through synergistic effects with reactive oxygen species(ROS)generation and immunomodulation.However,the hypoxic tumor microenvironment poses significant challenges by upregulating copper-sequestering proteins and downregulating key cuproptosis mediators.Future directions include integrating multi-omics approaches to identify novel therapeutic targets and developing combination therapies to overcome hypoxia-induced resistance.This review provides a comprehensive overview of copper metabolism in cancer,emphasizing the potential of cuproptosis induction as a powerful strategy for oncologic intervention.
基金jointly funded by the Strategic Priority Research Program of the Chinese Academy of Sciences(grant No.XDA0430301)the National Natural Science Foundation of China(grant Nos.42130109,41973059)。
文摘The formation of copper deposits is closely related to hydrothermal processes.Understanding the migration of copper in hydrothermal fluids aids in reconstructing mineralization processes and deciphering deposit genesis.Copper primarily exists as Cu^(+)and Cu^(2+)in hydrothermal solutions,with redox conditions governing their interconversion.In chloride-rich geological fluids,Cu-Cl complexes are considered critical for copper transport.However,the specific types and valence transitions of Cu-Cl complexes under varying hydrothermal conditions remain poorly understood.This study employed in situ Raman spectroscopy to systematically analyze Cu+HCl and CuCl_(2)+K_(2)S_(2)O_(3)/H_(2) systems under saturated vapor pressure at 25-300℃,elucidating the effects of temperature,Cl^(-)concentration,and redox conditions on copper speciation.In the Cu^(+)HCl system,copper dissolved as monovalent Cu-Cl complexes.At high temperatures(>200℃),[CuCl_(2)]^(-)is the dominated species,whereas[CuCl_(3)]^(2-)becomes prevalent at lower temperatures and higher HCl concentrations.For the Cu^(2+)-Cl system,the dominant species transitioned from[Cu(H_(2)O)n]^(2+)(<50℃)to[CuCl_(4)]^(2-)(100℃)and further to[CuCl]^(+)and[CuCl_(2)]^(0) at 300℃.The introduction of reducing agents(K_(2)S_(2)O_(3)/H_(2))facilitated Cu^(2+)→Cu^(+)reduction,thereby stabilizing Cu^(+)-Cl complexes and inducing partial copper precipitation.The behavior of copper in chloriderich hydrothermal fluids observed in this study indicates that high-temperature oxidizing fluids facilitate Cu mobilization,while cooling and redox changes promote deposition and ore minerals formation.
文摘At 82,master craftsman Zhu Bingren,China’s preeminent copper artist,continues to dynamically evolve his ancient heritage,proving that true preservation lies in innovation and bringing tradition into the contemporary world.THE copper art should not be confined to display cases,believes artist Zhu Bingren.From living rooms to fashion runways,and from the Great Wall in Beijing to the Louvre in Paris,the Chinese master craftsman brings his metal creations to life in diverse settings.
基金financially supported by the National Natural Science Foundation of China(No.52374259)the Open Fund of the State Key Laboratory of Mineral Processing Science and Technology,China(No.BGRIMM-KJSKL-2023-11)the Major Science and Technology Projects in Yunnan Province,China(No.202302 AF080004)。
文摘It is difficult to recover chrysocolla from sulfidation flotation which is closely related to the mineral surface composition.In this study,the effects of fluoride roasting on the surface composition of chrysocolla were investigated,its impact on sulfidation flotation was explored,and the mechanisms involved in both fluoride roasting and sulfidation flotation were discussed.With CaF_(2)as the roasting reagent,Na_(2)S·9H_(2)O as the sulfidation reagent,and sodium butyl xanthate(NaBX)as the collector,the results of the flotation experiments showed that fluoride roasting improved the floatability of chrysocolla,and the recovery rate increased from 16.87%to 82.74%.X-ray diffraction analysis revealed that after fluoride roasting,approximately all the Cu on the chrysocolla surface was exposed in the form of CuO,which could provide a basis for subsequent sulfidation flotation.The microscopy and elemental analyses revealed that large quantities of"pagoda-like"grains were observed on the sulfidation surface of the fluoride-roasted chrysocolla,indicating high crystallinity particles of copper sulfide.This suggests that the effect of sulfide formation on the chrysocolla surface was more pronounced.X-ray photoelectron spectroscopy revealed that fluoride roasting increased the relative contents of sulfur and copper on the surface and that both the Cu~+and polysulfide fractions on the surface of the minerals increased.This enhances the effect of sulfidation,which is conducive to flotation recovery.Therefore,fluoride roasting improved the effect of copper species transformation and sulfidation on the surface of chysocolla,promoted the adsorption of collectors,and improved the recovery of chrysocolla from sulfidation flotation.
基金financially supported by the National Natural Science Foundation of China(52130109)。
文摘Centrifugal casting of ductile iron pipe is a high-temperature,semi-continuous production process.However,conducting laboratory research on the solidification process of centrifugal casting of ductile iron pipe presents significant challenges.In this study,a novel research method was introduced for investigating the solidification process of ductile iron pipe,namely thermal simulation of ductile iron pipe.Comparative research was conducted on the microstructure and properties of the thermal simulation sample and the ductile iron pipe.The findings indicate that the thermal simulation sample and ductile iron pipe exhibit good heat transfer similarity and microstructure similarity.The difference of cooling rate between thermal simulation sample and ductile pipe is less than 0.24℃·s^(-1),and the difference of microstructure content of free cementite,ferrite,and pearlite is less than 5%.The tensile strength of annealed ductile iron pipe is 466 MPa,with an elongation of 16.1%and a Brinell hardness of 156.5 HBW.In comparison,the tensile strength of annealed thermal simulation sample is 482.0 MPa,with an elongation of 15.5%and a Brinell hardness of 159.0 HBW.These results suggest that the thermal simulation experimental research method is both scientific and feasible,offering an objective,reliable,and cost-effective approach to laboratory research on ductile iron pipe.
