Amount Of Cu Research Articles

Highly enhanced photocatalytic performance for CO2 reduction on NH2-MIL-125(Ti): The impact of (Cu, Mn) co-incorporation

Photocatalytic CO2 reduction has been considered as an efficient way for the carbon nuetrality. In this work, a series of (Cu, Mn) co-incorporated metal-orgnaic frameworks (MOFs) (NH2-MIL-125(Ti) (NML)) with different Cu2+/Ti4+ and Mn2+/Ti4+ molar ratios are systematically investigated to improve the efficiency for photocatalytic CO2 reduction. The optimized sample (1 M−5C−−NML) shows a highest yield of HCOOH (116.74 μmol.g−1.h−1) (3.71 times higher than that of NML), and a superior apparent quantum efficiency (AQE) (6.74 % at 405 nm). The improved performance is attributed to the formed oxygen vacancy and intermediate energy level as introduced by the co-incorporation, which facilitate the charge separation and enhance the visible-light-harvesting of NML. It shows that the density of oxygen vacancies increases with the increasing amount of Cu, resulting in enhanced charge separation. However, the increasing amount of Mn leads to the short-range Mn-Mn interaction, the concentration quenching effect as well as the inhibited photocatalytic performance. This work shows that the co-incorporated MOFs can be used as an advanced photocatalyst.

Enhanced Cu-EDTA degradation with trace Cu(II) in limestone via activating PMS

Effective removal of heavy metal complexes from contaminated water remains a challenging task. In this work, a limestone/PMS system was constructed for the efficient degradation of Cu-EDTA. Under the conditions of 3.0 g/L limestone and 1.0 mM PMS, the degradation efficiency of 10.0 mg/L Cu-EDTA reached 99.0 % in 60 min, and the removal efficiency of Cu ions approached 50.0 %. The main active specie revealed by quenching and EPR experiments was the singlet oxygen (1O2). Interestingly, Trace amounts of Cu(II) in limestone react with PMS enhancing the degradation of Cu-EDTA. The results of the HPLC-MS analysis showed that the reactive species attacked the Cu–O and Cu–N bonds, as well as triggered a decarboxylation process, resulting in the decomposition of Cu-EDTA into six intermediates. Meanwhile, SEM and XPS analyses revealed that Cu ions released during the degradation of Cu-EDTA are deposited on the limestone surface as Cu(OH)2 and Cu2(OH)2CO3. In addition, the initial pH and co-existing ions have a weak effect on the system. Finally, a one-month continuous flow experiment showed that the degradation efficiency of Cu-EDTA was about 95.0 % and the removal efficiency of Cu ions was 40.0 %. In conclusion, this study provides a new approach for the destruction of metal complexes and the removal of heavy metals.

Lattice Distortion Creates Enhancements in Photocatalytic and Electrocapacitive Performance of Sol–Gel‐Derived Cu‐Doped NiTiO3

A remarkable 35% enhancement in the photocatalytic and electrocatalytic abilities of an ilmenite nickel titanate (NiTiO3) material is reported. This boost in catalytic performance is achieved by simply creating a static distortion in the rhombohedral unit cell by replacing a small proportion of a small‐size nondegenerate Ni (69 pm) with a large‐size degenerate Cu (73 pm). The materials are synthesized by using a simple sol–gel method. The appropriate doping amount of Cu facilitates the better separation of intrinsic charge carrier pairs by inhibiting their recombination. The photocatalytic and electrochemical activities of durable materials in aqueous MB dye (10 ppm) and KOH (1 molar) electrolyte solutions are found to be directly associated with this improvement in inherent charge carrier transfer characteristics. The enhanced photodissociation of MB dye (42–56%) and specific capacitance (381–450 F g−1) in a KOH (1 molar) electrolyte are in full accord with the investigations carried out using crystallographic and optoelectronic analysis, charging–discharging measurements, and electrochemical impedance (EIS) spectroscopy investigations. Same material with high textural surface areas or controllable particle morphologies might show a far better photo/electrocatalytic performance in a variety of practical applications.

Fabrication of Cu-Infiltrated Journal Bearing by Binder Jetting Additive Manufacturing

In this study, considering the economic feasibility of products that can be produced through the binder jetting additive manufacturing process, 316L stainless steel, a widely used material with a wide particle size ranging from 15 to 106 μm, was used. The lubrication effect was increased by internal patterning through design for additive manufacturing, and journal bearing parts with excellent load resistance and wear resistance were implemented by using wear-resistant Cu as an infiltration material. In addition, to investigate the amount of Cu infiltrated as a function of porosity, the parts were pre-sintered from 1423 K to 1573 K, and the best performance was obtained when Cu was infiltrated after pre-sintering at 1473 K. As a result of rig testing of Cu-infiltrated journal bearings, mechanical properties were obtained that were more than 50% improved compared to those of mass products.

4+1] Heteroannulation to Form 1‐Pyrrolines through Alder‐Ene Reaction of in situ Generated Ynimines: Development and Application in Total Synthesis of Borrecapine

AbstractWe report in this paper a novel Cu‐catalyzed synthesis of polysubstituted 1‐pyrrolines. The reaction of β,γ‐unsaturated oxime esters 4 with terminal alkynes 5 in the presence of a catalytic amount of Cu(OAc)2 and 2,2′‐biquinoline affords the corresponding 1,6‐enynimines, which undergo a highly stereoselective Alder‐ene reaction to afford 1‐pyrrolines with concomitant generation of a quaternary carbon and a 2‐azadiene motif. It represents an unusual [4+1] heteroannulation reaction wherein terminal alkynes act as a one carbon donor and are 1,1‐difunctionalized. Mechanistic studies suggest that the allylic hydrogen trans to the oxime ester main chain is selectively transferred to the electron‐rich alkyne during the pericyclic reaction. The resulting 1‐pyrrolines undergo facile acid‐catalyzed regioselective Wagner–Meerwein rearrangement to provide 2H‐pyrroles in excellent yields. The 2H‐pyrroles are also accessible from 4 and 5 in a one‐pot manner without isolation of the 1‐pyrrolines. Leveraging this heteroannulation reaction as a key step, the first total synthesis of borrecapine, a 2,3,3,5‐tetrasubstituted pyrrolidine, is accomplished.

Insights into the Various Cellular Antimicrobial Responses, Biocompatibility, Osteogenesis, Wound Healing, and Angiogenesis of Copper-Doped Nano-Hydroxyapatite Composite Calcium Phosphate Bone Cement In Vitro

Calcium phosphate bone cement (CPC) is a popular material for bone remodeling, and nanohydroxyapatite (nHA) represents a breakthrough that has a wide range of clinical applications. During the early stages of bone repair, antibacterial and angiogenesis effects are essential to remodel new bone tissues. In this study, an antibacterial effect was achieved by incorporating Cu2+-doped nano-hydroxyapatite (Cu–nHA) synthesized through hydrothermal methods into CPC, and the impact of various amounts of Cu–nHA addition on the antibacterial and mechanical properties of CPC hybridization was evaluated. Moreover, the effects of Cu–nHA/CPC composites on the proliferation and mineralization of mouse progenitor osteoblastic cells (D1 cells) were characterized; the cell migration and angiogenesis ability of vascular endothelial cells (HUVECs) were also studied. Results indicated that incorporating 5 wt.% and 10 wt.% Cu–nHA into CPC led to a practical short-term antibacterial effect on S. aureus but not on E. coli. These Cu–nHA/CPC slurries remained injectable, anti-disintegrative, and non-toxic. Furthermore, compared with pure CPC, these Cu–nHA/CPC slurries demonstrated positive effects on D1 cells, resulting in better proliferation and mineralization. In addition, these Cu–nHA/CPC slurries were more effective in promoting the migration and angiogenesis of HUVECs. These findings indicate that 10 wt.% Cu–nHA/CPC has great application potential in bone regeneration.

Endogenous Cu(II) Labeling for Distance Measurements on Proteins by EPR.

In-cell measurements of the relationship between structure and dynamics to protein function is at the forefront of biophysics. Recently, developments in EPR methodology have demonstrated the sensitivity and power of this method to measure structural constraints in-cell. However, the need to spin label proteins ex-situ or use noncanonical amino acids to achieve endogenous labeling remains a bottleneck. In this work we expand the methodology to endogenously spin label proteins with Cu(II) spin labels and describe how to assess in-cell spin labeling. We quantify the amount of Cu(II)-NTA in cells, assess spin labeling, and account for orientational effects during distance measurements. We compare the efficacy of using heat-shock and hypotonic swelling to deliver spin label, showing that hypotonic swelling is a facile and reproducible method to efficiently deliver Cu(II)-NTA into E. coli. Notably, over six repeats we accomplish a bulk average of 57 μM spin labeled sites, surpassing existing endogenous labeling methods. The results of this work open the door for endogenous spin labeling that is easily accessible to the broader biophysical community.

Novel framework-confined Cu@ 13X catalyst with excellent resistance to toxic SO2 as an eco-friendly substitute for hazardous V-based NH3-SCR catalyst

V2O5-WO3/TiO2 (VWTi) catalyst has long been utilized in fixed source flue gases to purify harmful NO gas. However, VWTi is classified as a hazardous material because of its harm to human health and environment. To address this issue, a low-cost green Cu-based zeolite catalyst (Cu@13X) with a wide temperature range was synthesized using an in-situ hydrothermal method. This method is intended to control the adsorption capacity of toxic SO2 by regulating the location of Cu species. UV-Vis DRS and EXAFS analyses revealed that a significant amount of Cu was encapsulated within the 12-membered ring pores of the 13X molecular sieve. SO2-TPD and DFT calculations further indicated that Cu@ 13X exhibits reduced SO2 chemical adsorption capacity. Consequently, this green catalyst demonstrated superior catalytic performance, maintaining superior NOx conversion for over 70 h in the mixture gas containing 250 ppm SO2; while the Cu/13X catalyst lacked NH3-SCR catalytic activity under the same conditions. Moreover, Cu@ 13X catalyst also has excellent NH3-SCR catalytic performance in low temperature flue gas below 250 °C, which is significantly better than the hazardous VWTi catalyst. Characterization techniques such as NH3-TPD, H2-TPR, and XPS confirmed that the Cu@ 13X catalyst possesses excellent acidity, robust redox capabilities, and abundant surface defects. In-situ DRIFT spectra further illustrated that the NH3-SCR reaction on the catalyst surface adheres to the Eley-Rideal mechanism both before and after the introduction of toxic SO2. This study offers a fresh perspective on the development of framework-confined NH3-SCR catalysts and elucidates the mechanism behind the sulfur resistance of these catalysts. And the green Cu@ 13X catalyst is anticipated to serve as an effective alternative to the hazardous VWTi catalyst.

A mechanism study of type i corrosion on the surface of ancient tin rich bronzes

This study compares the surface patina of ancient tin rich bronze with pure hydrothermally synthesized SnO2 nanoparticles using various analytical techniques, including metallographic microscopy, scanning electron microscopy, transmission electron microscopy, energy dispersive spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and high-angle annular dark-field scanning transmission electron microscopy. The primary crystalline component of the patina consists of approximately 5 nm SnO2 nanoparticles, which closely resemble pure SnO2, indicating their comparability. Cu was also detected in the patina; however, it did not form crystalline structures. The X-ray diffraction results showed a shift in the patina’s peak, suggesting the infiltration of Cu into the SnO2 lattice, which compromises its crystallinity. In comparison to synthetic SnO2, the X-ray photoelectron spectroscopy spectra of the patina revealed novel peaks corresponding to both Cu and O, indicating the presence of Cu−O−Sn bonding—a characteristic feature of type-I patina. This suggests that the primary structure of type-I patina consists of crystalline SnO2 nanoparticles, with a limited amount of Cu integrated into its lattice configuration. The concentration of Cu within the SnO2 crystal units is restricted, leading primarily to the formation of amorphous Cu2O in conjunction with Sn. The presence of Sn enhances the structural stability of Cu2O, facilitating its incorporation while inhibiting the crystallization of Cu2O. However, when the Sn concentration is insufficient, an inadequate Cu–O−Sn amorphous phase may form, allowing for the potential crystallization of Cu2O.

Concurrent removal of Fe(II), Cu(II), and Zn(II) cations from acid mine drainage by an industrial solid waste - steel slag: Behaviors and mechanisms

Acid mine drainage (AMD) contamination poses a severe environmental threat and is a significant risk to human health. There is an urgent need to develop environmentally sustainable and technically viable solutions for water contamination caused by heavy metals. In this study, steel slag (SS) was used as a secondary resource to concurrently remove Fe(II), Cu(II), and Zn(II) from AMD. Because of the loose and porous structure, abundant functional groups, fast sedimentation velocity, and excellent solid-liquid separation, SS showed exceptional removal performance for heavy metal ions. The adsorption kinetic data of Fe(II), Cu(II), and Zn(II) showed good regression with the pseudo-second-order model. Besides, the adsorption of Fe(II) by SS conformed to the Freundlich model, whereas the adsorption of Cu(II) and Zn(II) followed the Langmuir model, with the maximum adsorption amounts of Cu(II) and Zn(II) being 170.69 and 155.98 mg/g. Furthermore, competitive adsorption was observed among Fe (II), Cu (II), and Zn (II) in a multi-component system, with the adsorption priority being Fe (II) > Cu (II) > Zn (II). The removal mechanism of Fe(II), Cu(II), and Zn(II) in AMD by SS mainly includes electrostatic attraction, chemical precipitation, and surface complexation. Interestingly, the leached concentrations of Fe(II), Cu(II), and Zn(II) from the spent slag after calcination were all within the detection limit of the Chinese emission standard, demonstrating excellent environmental stability. Theoretically, this renders it a viable candidate for use as an additive in construction materials. Meaningfully, the work offers a practical approach for energy-efficient and eco-friendly heavy metal ions adsorption, and the secondary utilization of SS also contributes to the sustainable development of the steel industry. It is beneficial to implement the development concepts of clean production and efficient utilization of industrial solid waste.

Microstructures, mechanical properties and damping performance of wrought Mg–Cu–Ca alloys

Mg–Cu–Ca alloy sheets show good room temperature formability and excellent thermal conductivity; however, their strength is insufficient for load-bearing applications. In this study, Mg–Cu–Ca ternary alloys were subjected to a conventional extrusion process, and the microstructures and tensile properties were systematically evaluated. The addition of extremely small amounts of Cu and Ca to pure Mg (Mg–0.03Cu–0.05Ca, wt%) led to significant refinement of dynamically recrystallized (DRXed) grains while preserving a certain fraction of un-DRXed grains, which contributed to a substantial increase in tensile yield strength. Adjusting the extrusion parameters further increased the tensile yield strength to 329MPa, driven by the combined effects of further refined DRXed grains and an increased area fraction of un-DRXed grains. The damping performance of the Mg–0.03Cu–0.05Ca alloy sheet was superior to that of commercial AZ31(Mg–3Al–1Zn–0.3Mn in wt%) alloy sheet but lower than that of pure Mg, particularly at low frequencies. This revealed that the solute segregation at grain boundaries plays a crucial role in the damping performance of Mg alloys.

Robustly Boosting Thermoelectric Performance of N-Type PbSe via Lattice Plainification and Dynamic Doping.

Ideal thermoelectrics shall possess a high average ZT, which relies on high carrier mobility and appropriate carrier density at operating temperature. However, conventional doping usually results in a temperature-independent carrier concentration, making performance optimization over a wide temperature range be challenging. This work demonstrates the combination of lattice plainification and dynamic doping strategies is an effective route to boost the average ZT of N-type PbSe. Because Sn and Pb have similar ionic radii and electronegativity, this allows Sn to fill the intrinsic Pb vacancies and effectively improves the carrier mobility of PbSe to 1300 cm2 V-1 s-1. Furthermore, a trace amount of Cu is introduced into the Sn-filled PbSe to optimize the carrier concentration. The extra Cu is situated in the interstitial sides of the lattice, which undergoes a dissolution-precipitation process with temperature, leading to a strongly temperature-dependent carrier density in the material. This dynamic doping effectively improves the electrical transport properties and is also valid to suppress the lattice thermal conductivity. Ultimately, the resulting PbSn0.004Se+3‰Cu obtains a maximum ZT of ≈1.7 at 800 K and an average ZT of ≈1.0, with a 7.7% power generation efficiency in a single-arm device, showing significant potential for commercial application.

Effect of Cu doping on morphology and properties of calcium ferrite and its application as oxygen carrier in chemical looping hydrogen production

Chemical looping hydrogen production with inherent CO2 capture has been widely recognized as a clean and efficient approach to high-purity hydrogen production because of the ultra-pure H2 product without any purification facilities. It is crucial to develop oxygen carriers with better performance to improve fuel conversion and hydrogen production efficiency. The potential of Ca2Fe2O5 in steam converting has been confirmed. However, its lower oxygen transfer capacity, that is, it tends to produce lower fuel conversion in fuel reactors, which will limit its practical application. Here, we report the development of Cu-doped Ca2Fe2O5-based oxygen carriers using sol-gel technology. The effects of B-site substitution of Cu element on the morphological properties and redox properties of Ca2Fe2-xCuxO5 (x = 0, 0.1, 0.25, 0.5, 1) oxygen carriers were evaluated based on experiments and density functional theory calculations. The results show that Cu doping not only elevated the surface oxygen content and enhanced the oxygen activity of the oxygen carriers, but also increased the Fe3+ at the B-site, thus enhanced their binding ability with oxygen molecules. Vacancy formation was a rate-determining step in the chemical looping hydrogen production (CLH), and Cu-doped Ca2Fe2O5 reduced the energy of oxygen vacancy formation. In the CLH process, the doping of Cu significantly improved the hydrogen productivity and fuel conversion rate. The fuel conversion rate was positively correlated with the doping amount of Cu. When x = 1, Ca2Fe2-xCuxO5 had the maximum fuel conversion rate, and its average conversion was 54.2% more than that of undoped Ca2Fe2O5. Ca2Fe2-xCuxO5 with x = 0.25 was the most suitable for CLH with the highest H2 yield, which was 20.3% more than that of Ca2Fe2O5. Moreover, its properties remained stable over multiple redox cycles with high activity and stability for CO-CLH.

BIOACCUMULATION OF CU AND CO IN LEAFY AND FRUIT VEGETABLES FROM THE SUBURBS OF MITROVICA, KOSOVO

Contamination of vegetables with heavy metals is one of the basic environmental problems, especially in developing cities, primarily due to the uncontrolled level of pollution caused by industrial growth and the increase in the number of vehicles using petroleum fuels. This paper aims to determine the bioconcentration of heavy metals Cu and Co in leafy and fruit vegetables grown near Kosovska Mitrovica (Republic of Kosovo). Three places near Kosovska Mitrovica (Zvečan, Frashër, and Polski) are grown: parsley, spinach, lettuce, peppers, eggplant, and cucumber. All analyzed crops are from the 2023 harvest. In the same period, an analysis was made of the soil on which the crops were grown. The bioconversion factor (BF)of the selected leafy and fruit vegetables was also determined. The ICP-MS technique was used to determine the concentration of Cu and Co in soil and leafy and fruit vegetables. From the obtained analyzes it was determined that the soil in Frashër contains the highest amount of Cu and Co - 58.4 mg/kg and 11.6 mg/kg respectively. The amount of Cu in the examined dry leafy and fruit vegetables is in the range from 5.38 mg/kg to 22.4 mg/kg, and of Co from 0.27 mg/kg to 2.99 mg/kg. The bioconcentration factor of the studied leafy and fruit vegetables of Cu and Co is in the range of 0.04 to 0.26 and 0.15 to 0.65 respectively. The accumulation of Co in the analyzed vegetables is higher than the accumulation of Cu, due to the higher BF values for Co. The statistical processing of the results (t-test) showed that there is a difference in the concentration of Cu and Co between leafy and fruit vegetables, but there is no statistically significant difference because the obtained p-values are greater than the marginal p-values.

ACCUMULATION OF HEAVY METALS IN APPLES AND PEARS FROM THE SUBURBS OF MITROVICA, KOSOVO

Intake of heavy metals through the food is a food safety problem that seriously affects consumer health. Therefore, information is needed on the intake of food contaminated with heavy metals and their concentrations, to assess the potential risk for human health. This paper aims to determine the accumulation of metals in apples and pears grown in the surroundings of Kosovska Mitrovica (Republic of Kosovo) and the bioconcentration factor (BF). With the help of the ICP-MS technique, were determined the amounts of Cu, Fe, Co, Mn, Ni, and Cr in apples and pears grown in three regions - Zvečan , Frashër, and Polski. From the conducted tests, the highest concentrations in apples and pears were determined for iron (on average 100.67 mg/kg for apples and 107.4 mg/kg for pears) and the lowest concentrations for cobalt (on average 0.13 mg/kg for apples and 0.18 mg/kg for pears). The lowest bioconcentration factor in apples is 0.01 (for Fe, Co, and Mn in all three regions), and the highest is 0.32 (for Cr in Zvečan). When determining the bioconcentration factor in pears, the lowest (0.01) was determined for iron (in all three regions) and manganese (in Zvečan and Frashër regions), and the highest bioconcentration factor was determined for copper – 0.46 (Polski region). There is a very high correlation between the values obtained for the analyzed metals in apples and pears. According to BF values, pears extract twice as much Cu and Co from the soil compared to apples, and the extraction of other metals from the soil is the same for both types of fruit.

Levels of heavy metals and physicochemical properties of honey from four selected areas of Ethiopia

In this work, the qualities of honey samples were evaluated by assessment of some physicochemical parameters and levels of heavy metals (Cd, Pb, Cr, Ni, Zn and Cu). The honey samples were collected from the major producing regions of Ethiopia; Gojjam, Gondar, Jimma and Tigray. The pH and electrical conductivity (EC) of the samples were determined using digital pH-meter and conductivity meter, respectively. The metal contents were determined by flame atomic absorption spectrometry (FAAS). The validity of the method employed was evaluated by spiking experiments with recoveries ranging from 90.0 to 95.8%. The FAAS results show higher concentration of Cu and Zn compared to other metals. The amount of Cu and Zn were in the range 6.2–18 μg/g and 4.2–10 μg/g. The heavy metals (Cd, Pb, Cr and Ni) were below detection limit in all the honey samples. Moreover, the result obtained regarding the physicochemical properties showed that the pH of all the honey samples were acidic (pH of 3.84–4.00), the EC 0.09–0.34 mScm-1 and the ash content 0.13–0.33%. The results obtained were in agreement with European standard and Codex Alimentarius, indicating the honey samples studied are of good quality and suitable for human consumption. KEY WORDS: Honey, Heavy metals, Physicochemical properties, FAAS, Ethiopia Bull. Chem. Soc. Ethiop. 2024, 38(6), 1521-1531. DOI: https://dx.doi.org/10.4314/bcse.v38i6.2

The influence of recycling on the localized corrosion susceptibility of extruded AA6063 alloys

An approach involving the quantification of microstructure characterized by different techniques such as SEM, EDS, and SKPFM is statistically treated to provide a deeper insight into the influence of recycling AA6063 on localized corrosion susceptibility. Particularly, the intermetallic particles and the two forms of localized corrosion – pitting and intergranular corrosion are systematically documented, measured, and analyzed. Even trace amounts of Cu and Zn introduced into the alloy from recycling had a remarkable effect on the localized corrosion susceptibility. The study found that the initiation and early evolution of the two localized corrosions are in competition, and the predominance of one over the other is closely linked to the composition of the alloy, and microstructure. Recycled variants with higher trace Cu made the alloy more susceptible to pitting attack whereas higher trace Zn is linked with greater IGC susceptibility. The trace amount of higher Zn addition has a particularly beneficial effect on pitting susceptibility as it reduces the likelihood of pitting even in alloys with a higher trace Cu content. The SKPFM results obtained in this study provided a basis for the circumferential pitting susceptibility around intermetallic particles, as a higher volta potential difference (∆V) implied a higher driving force for corrosion. ∆V differences between the different variants were further explained based on trace recycled element distribution in the microstructure.

Surface Facets Reconstruction in Copper-Based Materials for Enhanced Electrochemical CO2 Reduction.

The unavoidable and unpredictable surface reconstruction of metallic copper (Cu) during the electrocatalytic carbon dioxide (CO2) reduction process is a double-edged sword affecting the production of high-value-added hydrocarbon products. It is crucial to control the surface facet reconstruction and regulate the targeted facets/facet interfaces, and further understand the mechanism between activity/selectivity and the reconstructed structure of Cu for CO2 reduction. Based on the current catalyst design methods, a facile strategy combining chemical reduction and electro-reduction is proposed to achieve specified Cu(111) facets and the Cu(110)/(111) interfaces in reconstructed Cu derived from cuprous oxide (Cu2O). The surface facet reconstruction significantly boosted the electrocatalytic conversion of CO2 into multi-carbon (C2+) products comparing to the unmodified catalyst. Theoretical and experimental analyses show that the Cu(110)/(111)s interface between Cu(110) and a small amount of Cu(111) can tailor the reaction routes and lower the reaction energy barrier of C-C coupling to ethylene (C2H4). The work will guide the surface facets reconstruction strategy for Cu-based CO2 electrocatalysts, providing a promising paradigm to understand the structural variation in catalysts.

Ligand-free Ni-Cu bimetallic nanocatalyst: Laser synthesis, characterization and its high performance for borohydride assisted catalytic reduction of 4-nitrophenol

In the present work, nickel and copper bimetallic nanoparticles with three different concentration ratios of 70:30, 50:50, and 30:70 were synthesized by laser ablation of Ni and Cu in deionized water. The suitability of Ni-Cu bimetallics as nanocatalysts was investigated in the catalytic reduction of pollutant 4-nitrophenol. The nanocatalysts were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and ultraviolet-visible (UV–Vis) spectroscopy. The morphology using SEM and TEM indicated that Cu had an elongated or flake-like structure, whereas Ni had a quasi-spherical structure. XPS investigation has been performed to study the elemental composition and chemical states near-surface regions of the generated Ni-Cu bimetallic nanoparticles. XRD and XPS confirm high oxidation of Cu to CuO with approximately no residual Cu metal. However, the XRD patterns did not show complete Ni oxidation to NiO, confirming the presence of a Ni dopant part in the Ni-Cu samples. The behavior of the photoelectron peaks in the XPS spectra suggested that the Ni-Cu nanocomposites exhibited surface charge transfer. Pulsed laser ablation developed ligand-free Ni-Cu nanoparticles, which affected the structure and catalytic properties. The nanocatalyst for 50:50 of Ni and Cu had the highest rate constant, corresponding to the shortest time required to achieve 100 % conversion/reduction of the pollutant dye. The apparent synergistic effect between Ni and Cu is clearly dictated by the amount of Cu embedded in the nanocomposites, with this becoming a key factor in lowering the band gap energy values. Overall, the surface charge transfer rate can enhance the catalytic performance by tuning the Ni and Cu concentrations.

SIMS U-Pb dating of baddeleyite-zircon pairs in mafic rocks to determine the ages of magmatic mineralization and hydrothermal remobilization in a Ni-Cu-(PGE) deposit

Ni-Cu-(PGE) sulfide deposits associated with mafic–ultramafic rocks are the most important sources of Ni and platinum-group elements (PGE) in the world. These deposits also contain significant amounts of Cu. Such deposits are generally considered to have formed by multiple stages of primary magmatic concentration and secondary hydrothermal remobilization. However, constraining the ages of Ni-Cu-(PGE) sulfide deposits has proven challenging, particularly those that have experienced post-magmatic hydrothermal overprinting and remobilization. The lack of robust geochronology data has hindered understanding of the geological controls on this important type of mineralization. The Chibaisong Ni-Cu-(PGE) sulfide deposit in the North China Craton is characterized by disseminated and net-textured ores formed by magmatic processes and overprinted by hydrothermal Cu-rich vein stockwork. The Cu-rich vein stockwork is fracture-controlled, and contains a mineral assemblage of Ni-Cu sulfides (chalcopyrite, pyrrhotite, pentlandite), amphibole and quartz. Chalcopyrite in the hydrothermal stockwork is relatively depleted in Ni but enriched in Ag and Cd compared with disseminated magmatic chalcopyrite, typical of hydrothermal superimposed ores as documented elsewhere. We identified baddeleyite-zircon pairs associated with Ni-Cu sulfides in hydrothermal superimposed ores of the Chibaisong deposit, in which the baddeleyite is unequivocally of primary igneous origin whereas the zircon represents the replacement product of baddeleyite during hydrothermal alteration. In situ SIMS U-Pb dating of baddeleyite and zircon yielded weighted mean 207Pb/206Pb ages of 2181 ± 21 Ma and 1892 ± 33 Ma, respectively, interpreted as the timing of magmatic mineralization and subsequent hydrothermal remobilization of the Ni-Cu-(PGE) deposit. Our results explain the large discrepancies in sulfide Re-Os ages previously obtained from this deposit. This study demonstrates that on the basis of detailed BSE imaging, in situ SIMS U-Pb dating of baddeleyite-zircon pairs can provide robust age constraints for both magmatic mineralization and hydrothermal remobilization of Ni-Cu-(PGE) sulfide deposits hosted in mafic–ultramafic intrusions, although further studies are needed to test whether the formation of such deposits commonly entails multiple stages of hydrothermal remobilization. Since baddeleyite or baddeleyite-zircon pairs are common accessory minerals in Ni-Cu-(PGE)-bearing mafic–ultramafic rocks, the dating approach employed in this study may be applicable to similar deposits elsewhere.