Different Amounts Of Cu Research Articles

Effect of Annealing Process on the Morphological, Optical and Electrical Properties of Cu:MnO Films Prepared by PLD Technique

In this study, Nd:YAG laser pulses with a wavelength of 1064 nm, a power of 500 mJ, a pulse width of 9 ns, and a repetition frequency of 6 Hz were used to hit a manganese oxide (MnO) target surface 300 times. Pure MnO and copper Cu-doped MnO (Cu:MnO) with different amounts of Cu (0.03, 0.05, 0.07, and 0.09 wt%) produced by PLD were studied. Cu:MnO thin films were annealed at 473 K, and their morphological, optical, and electrical characteristics were studied. The results of the atomic force microscopic (AFM) investigation of morphological properties showed that Cu dopant impacted the creation of roughness and particle size in MnO2 films. The optical transmission was examined using a UV-Vis spectrophotometer. The highest optical absorption was noted at 0.09 dopant content. The dielectric constants' real (εr) and imaginary (εi) components, as well as the extinction coefficient (k), refractive index (n), and other optical constants, were studied. At an annealing temperature of (473 K), Hall effect studies demonstrate that all produced films exhibit a P-type conductivity.

Biological Renewable Cellulose-Templated Zn1-XCuXO/Ag2O Nanocomposite Photocatalysts for the Degradation of Methylene Blue.

Herein, Cellulose-templated Zn1-XCuXO/Ag2O nanocomposites were prepared using biological renewable cellulose extracted from water hyacinth (Eichhornia crassipes). Cellulose-templated Cu-doped ZnO catalysts with different amounts of Cu as the dopants (1, 2, 3, and 4%) were prepared and denoted CZ-1, CZ-2, CZ-3, and CZ-4, respectively, for simplicity. The prepared catalysts were tested for the degradation of methylene blue (MB), and 2% Cu-doped ZnO (CZ-2) showed the best catalytic performance (82%), while the pure ZnO, CZ-1, CZ-3, and CZ-4 catalysts exhibited MB dye degradation efficiencies of 54, 63, 65, and 60%, respectively. The best catalyst (CZ-2) was chosen to further improve the degradation efficiency. Different amounts of AgNO3 (10, 15, 30, and 45 mg) were used for the deposition of Ag2O on the surface of CZ-2 and denoted CZA-10, CZA-15, CZA-30, and CZA-45, respectively. Among the composite catalysts, CZA-15 showed remarkable degradation efficiency and degraded 94% of MB, while the CZA-10, CZA-30, and CZA-45 catalysts showed 90, 81, and 79% degradation efficiencies, respectively, under visible light within 100 min of irradiation. The enhanced catalytic performance could be due to the smaller particle size, the higher electron and hole separation and charge transfer efficiencies, and the lower agglomeration in the composite catalyst system. The results also demonstrated that the Cu-doped ZnO prepared with cellulose as a template, followed by the optimum amount of Ag2O deposition, could have promising applications in the degradation of organic pollutants.

A Long-Term Study on the Bactericidal Effect of ZrN-Cu Nanostructured Coatings Deposited by an Industrial Physical Vapor Deposition System.

ZrN-Cu coatings containing two different amounts of Cu (~11 at.% and ~25 at.%) were deposited using an industrial physical vapor deposition (PVD) system. The as-deposited coatings exhibited 100% bactericidal efficiency against Escherichia coli CCM 3988 for an exposure time of 40 min. Subsequently, the samples were attached onto our faculty's door handles for six months to study the coatings' long-term effectiveness and durability under actual operational conditions. The samples were periodically evaluated and it was observed that the coatings with 25 at.% Cu performed better than the ones with 11 at.% Cu. For example, following 15 days of being touched, the bactericidal effectiveness of the sample containing 25 at.% Cu dropped to 65% while it fell to 42% for the sample containing 11 at.%. After 6 months, however, both samples showed bactericidal efficiency of ~16-20%. The bactericidal efficiency of the samples touched for 6 months was successfully restored by polishing them. Furthermore, a group of samples was kept untouched and was also evaluated. The untouched samples with Cu content of ~25 at.% did not show any drop in their bactericidal properties after 6 months. ZrN-Cu coatings were concluded to be promising materials for self-sanitizing application on high-touch surfaces.

Improved Charge Carrier Transport Across Grain Boundaries in N‐type PbSe by Dopant Segregation

Doping is an important and routine method to tune the properties of semiconductors. Dopants accumulated at grain boundaries (GBs) can exert a profound influence on microstructures and transport properties of heat and charge. To unravel the effect of dopant accumulation at GBs on the scattering of electrons, individual high‐angle GBs in three PbSe samples doped with different amounts of Cu using a home‐designed correlative characterization platform combining electron backscatter diffraction, microcircuit transport property measurements, and atom probe tomography are studied. The findings reveal that the segregation of Cu dopants to GBs reduces the GB potential barrier height. Once the GB phase reaches an equilibrium with saturated Cu, the extra Cu dopants distribute homogeneously inside the grains, compensating for vacancies and improving the electrical conductivity of the PbSe grains. The results correlate the Cu distribution at GBs and grains with local electrical properties, enlightening strategies for manipulating advanced functional materials by GB segregation engineering.

Long-term Cu exposure alters CYP450s activity and induces jejunum injury and apoptosis in broilers.

Copper (Cu) is an essential trace element that plays a crucial role in numerous physiopathological processes related to human and animal health. In the poultry industry, Cu is used to promote growth as a feed supplement, but excessive use can lead to toxicity on animals. Cytochrome P450 enzymes (CYP450s) are a superfamily of proteins that require heme as a cofactor and are essential for the metabolism of xenobiotic compounds. The purpose of this study was to explore the influence of exposure to Cu on CYP450s activity and apoptosis in the jejunum of broilers. Hence, we first simulated the Cu exposure model by feeding chickens diets containing different amounts of Cu. In the present study, histopathological observations have revealed morphological damage to the jejunum. The expression levels of genes and proteins of intestinal barrier markers were prominently downregulated. While the mRNA expression level of the gene associated with CYP450s was significantly increased. Additionally, apoptosis-related genes and proteins (Bak1, Bax, Caspase-9, Caspase-3, and CytC) were also significantly augmented by excessive Cu, while simultaneously decreasing the expression of Bcl-2. It can be concluded that long-term Cu exposure affects CYP450s activity, disrupts intestinal barrier function, and causes apoptosis in broilers that ultimately leads to jejunum damage.

Influences of Cu on microstructure and mechanical properties in Fe–Ni–Al ultra-strong maraging steels

Although the influences of Cu on microstructure and mechanical properties have been extensively studied in low-alloy steels, the aging behavior of high-alloy maraging steels with Cu remains elusive. In this work, we systematically investigated the nanoprecipitation behavior and their effects on mechanical properties in Fe–Ni–Al ultra-strong maraging steels by introducing different amounts of Cu. Structural analyses with atom probe tomography (APT), transmission electron microscopy (TEM) and small angle neutron scattering (SANS) indicate that the addition of Cu promotes the precipitation of nanoscale B2–NiAl phases in the Fe–Ni–Al ultra-strong maraging steels. The primarily precipitated Cu-clusters can serve as the nucleation sites for the precipitation of B2–NiAl at the early stage of aging, and then are dissolved into the B2–NiAl nanoprecipitates, which increases the lattice misfit between the B2–NiAl and the matrix and thereby the growth rate of B2–NiAl. As a result, the addition of 0.6 wt% Cu significantly improves the ductility of the Fe–Ni–Al ultra-strong steel without sacrificing strength. With 0.6 wt% Cu added to the Fe–Ni–Al ultra-strong steel, the elongation increased from 3.2% to 8.7% while the strength remained 2.0 GPa, due to the high-density precipitation of Ni(Al, Cu) nanoparticles. The underlying mechanisms for the precipitation behavior and the precipitation strengthening effect were discussed in terms of lattice misfit, Cu segregation and stress field.

CuO–TiO2 pilot-plant system performance for solar photocatalytic hydrogen production

The main goal of the present study was to explore photocatalytic performance of the TiO2–CuO mixture, for solar to hydrogen conversion at pilot plant scale under two different irradiation conditions (sunny and partly cloudy), focusing on high-temperature pretreatment of the catalyst mixture to try to improve TiO2 doping with copper. P25–TiO2 and commercial CuO were used with different amounts of Cu (2 wt% or 7 wt% Cu) calcined at 200–400 °C during several hours. Catalysts were tested at pilot plant scale using solar compound parabolic collectors, with glycerol as the sacrificial agent. The photocatalyst prepared after heating at 200 °C for 3 h and with 7 wt% Cu, resulted in higher hydrogen production than under the other heating conditions, and results were slightly better (5–10%) than the reference values with the untreated catalysts. Photocatalytic efficiency was slightly lower at the higher calcination temperature (400 °C). CO2 production and formation of formate and glycolate clearly demonstrated glycerol photoreforming. The Cu from the calcined catalyst remaining on the solid was significantly less (2.5%) than on the non-calcined catalyst (4.2%), with an important fraction of lixiviated copper and copper deposition on the reactor walls. This is a critical drawback that must be considered for large-scale applications.

Methane Dehydrogenation and Coking Resistance on Ni(111) Surfaces of SOFC Anodes with Different Cu Doping Ratios under a Consistent DFT Framework

Carbon deposition on nickel-based anodes is a key problem for solid oxide fuel cells (SOFCs) using hydrocarbon fuels. One of the solutions is doping with other elements. In this work, DFT calculations were used to systematically study the processes of continuous CH4 dehydrogenation, carbon formation, and carbon elimination on Ni(111) surfaces doped with different amounts of Cu. The Cu doping concentrations on the Ni surface are set as 0, 1/9, 4/9, 5/9, 8/9, and 1 ml, namely Ni(111), NiCu1, NiCu4, NiCu5, NiCu8, and Cu9. The adsorption energies and adsorption sites of the important substances were obtained by calculation. In addition, the kinetics and thermodynamics of the main reactions and potential carbon removal pathways are discussed. Prior studies have shown that the introduction of Cu weakens the interaction between the Ni-based surface and the absorber, thereby enhancing the activity of various species on the surface of Ni-based catalysts. Second, the methane cracking path on the Ni-based surface is CH4 → CH3 → CH2 → CH, and the paths on the other five surfaces are the same. We found that the addition of Cu can weaken the adsorption of C, inhibit the activity of CH4 dehydrogenation, and promote the binding of C to the intermediate medium on the Ni-based surface, thus improving the ability of carbon deposition resistance. Finally, based on our DFT calculations, several potential carbon removal pathways are discussed in detail, and it is believed that the problem of carbon removal on SOFC anodes should focus on the oxidation of CH while preventing its direct cracking.

Shape memory behaviour of polyvinyl alcohol aerogels cross-linked with Fe3+ & Cu2+ metallic ions

The utter purpose of this study was to embed metal ions in polymer chains to improve the shape memory behaviour of polyvinyl alcohol (PVA) aerogels in which metal ions were used as cross-linking agents for PVA. PVA–Cu and PVA–Fe hydrogels were first prepared by adding different amounts of Cu (NO3)2.3H2O and Fe (NO3)3.9H2O salts, respectively, then aerogel samples were prepared by the freeze-drying of hydrogels. Fourier transform infrared test was employed to evaluate the chemical structure. Gravimetric and mercury porosimetry methods were performed to characterize the porosity of aerogels. Field emission scanning electron microscopy examined the microstructure of the network and the porosity of the aerogels. The shape memory behaviour of the nanocomposite aerogels was evaluated by dynamic-mechanical analysis. The test results showed that by adding 25 wt% copper salt and 40 wt% iron salt to the PVA, the maximum gel fractions were achieved. Compared to pure PVA, the recovery ratios of nanocomposite aerogels increased by about 80% and 140% and their moduli increased by more than 370% and 300%, respectively.

Development and Testing of Ni-Cu Bimetallic Catalysts for Effective Syngas Production via Low-Temperature Methane Steam Reforming

In the present work, novel bi-metallic catalysts for syngas production at low temperature steam reforming are developed, characterised and tested. Steam methane reforming by using bi-metallic Ni-Cu catalysts found to balance the product of CO to CO2 ratios, while affected the water gas shift reaction by increasing the hydrogen selectivity up to 600°C. The addition of different amounts of Cu (3, 5, 7, 10 wt%) to the Ni catalyst for methane steam reforming showed different reactivity trends. One of the major outcomes of this work is the maximum load capacity of Cu (5wt.%Cu) to maintain the reactivity. For comparison purposes, mono-metallic catalysts of Cu and Ni were developed and tested along with the bi-metallic ones. The activity of the reaction decreased by doping more than 5wt.%Cu which affected the amount of hydrogen produced. This is related to the possible limited number of available sites required for hydrogen adsorption to maintain the reaction of methane steam reforming. Another important outcome of this work is the bi-metallic Ni-Cu catalysts did not decrease the amount of carbon formation.

An Assessment of the Bactericidal and Virucidal Properties of ZrN-Cu Nanostructured Coatings Deposited by an Industrial PVD System

Pathogenic microbes, such as bacteria and viruses, can spread quickly via contaminated surfaces. Most of these pathogenic microorganisms can survive on surfaces for a long time. Touching these surfaces can lead to the transmission of the microorganisms to the human body and cause serious illnesses. ZrN-Cu coatings containing different amounts of Cu were deposited using an industrial PVD system, and their ability to inhibit bacteria and inactivate the SARS-CoV-2 virus was tested. Microstructural studies showed the formation of two distinct ZrN and Cu phases when Cu content was sufficiently high. Hardness and elastic modulus were inversely proportional to the Cu content. The coatings showed outstanding bactericidal properties against Escherichia coli and Pseudomonas aeruginosa, especially when Cu content was more than 12 at.% and exposure time was longer than 40 min. The coatings, however, did not exhibit any significant virucidal properties. Good mechanical properties, along with excellent antibacterial effects, make these coatings suitable for use as self-sanitizing surfaces on objects that people regularly touch and that are prone to bacterial contamination. Their use would thus allow for only minimal transmission or multiplication of bacteria, and the treated surface would not serve as another source of infection.

A facile synthesis of CuBi2O4 hierarchical dumbbell-shaped nanorod cluster: a promising photocatalyst for the degradation of caffeic acid.

The present study reports on the synthesis of Cu-bismuth oxide (CuBi2O4)-based nanorods by using a simple co-precipitation method for the photocatalytic degradation of caffeic acid (CA). The incorporation of Cu metal ions during the synthesis of CuBi2O4 nanorods might be advantageous to avoid the aggregation and control the leach out of metal ions. The calculated bandgap values of ~ 1.04, 1.02, and 0.94eV were observed for CuBi2O4 with different amounts of Cu 1.0, 0.50, and 0.25g, respectively. Varying the quantity of Cu metal ions easily tuned the bandgap value within the CuBi2O4-based nanorods. However, a further decrease in the bandgap value increased the recombination rate, and the less photocatalyst performance was observed. The CA degradation could be explained based on the species distribution. The CA pKa was mainly located between pKa1 and pKa2 of 4.43 and 8.6, respectively. The Cu within the CuBi2O4-based nanorods changed the electronic properties and the antibacterial ability. Therefore, the synthesized CuBi2O4-based nanorod cluster might be a promising material for the photocatalytic degradation of CA.

Creating Cu(I)-decorated defective UiO-66(Zr) framework with high CO adsorption capacity and selectivity

• Defective UiO-66 was rapidly fabricated by continuous-flow microwave synthesis. • The surface area and pore width of UiO-66 (Zr) were improved by defects. • The most defective 25Cu(I)@UiO-66 had the highest CO uptake capacity of 2.44 mmol/g. • Defective Cu(I)@UiO exhibited improved CO selectivity. • Cu(I)@UiO-66(Zr) showed good renewability and oxygen-resistant ability. Developing a highly effective material for CO storage and separation is a challenge. In this study, we first used microwave-assisted continuous-flow synthesis to create defective UiO-66(Zr) frameworks with improved surface area and pore structures, which is highly efficient for large-scale production. The defect concentration of UiO-66(Zr) was rapidly and effectively controlled within a short reaction time of 10 min. Different amounts of Cu 2+ were loaded onto defective UiO-66 samples, followed by reducing Cu 2+ to Cu + to obtain Cu(I)@UiO-66 adsorbents (Cu(I)@UiO). X-ray diffraction (XRD), N 2 -adsorption, FT-IR, SEM, TEM, thermogravimetric analysis (TGA), and XPS analyses were used to characterize the physicochemical properties of the prepared adsorbent materials. Gas adsorption experiments revealed that Cu(I)-decorated defective UiO-66 exhibited high CO adsorption capacity due to the π complexation between Cu + and CO. The CO adsorbing amount and CO selectivity onto the Cu(I)@UiO-66 samples were improved by adjusting the defect concentration and Cu(I) load on the UiO-66 host. The breakthrough experiment confirms that this defective Cu(I)@UiO adsorbent can efficiently separate CO/N 2 mixture under dynamic mixture flow conditions. Furthermore, after several cyclic adsorption–desorption experiments, the defective Cu(I)@UiO-66 is highly regenerable and has a good oxygen-resistant ability. The study describes a simple and scalable method for producing π-complexation adsorbent for CO adsorption.

Cu doped Ni–Co spinel protective coatings for solid oxide fuel cell interconnects application

Four different amount of Cu doped Ni–Co alloy coatings were fabricated on SUS430 substrate by electroplating for solid oxide fuel cells (SOFCs) interconnects application. After oxidation at 800 °C, the microstructure and oxide phase of samples were tested by scanning electron microscope (SEM) with energy dispersive spectroscopy (EDS) and X-ray diffraction (XRD). Our experimental results indicated that the Cu addition improved the electrical behavior of Ni–Co alloy coating. Cu doping reduced the activation energy (Ea) of electrons hopping and inhibited the growth of Cr2O3 oxide layer. Furthermore, the oxidation kinetics and electrical properties of the alloy coatings were obtained. These results showed that the 9% Cu doped Ni–Co coated steels achieved the minimum parabolic rate constant (2.05 × 10−14 g2cm−4s−1) and area specific resistance (14.11 mΩ cm2) after the thermostatic oxidation process.

Dynamics of bound states of dihydrogen at Cu(I) and Cu(II) species coordinated near one and two zeolite framework aluminium atoms: A combined sorption, INS, IR and DFT study

Ambient conditions sorption isotherms of dihydrogen in a series of various levels of Cu-exchanged ZSM-5 zeolites, with two different Si/Al ratios, namely 11.5 and 25, show the presence of different amount of Cu centres able to strongly bind H2. Although the isosteric heats of adsorption derived from these isotherms are rather similar, of the order of 30 kJ/mol H2, Inelastic Neutron Scattering (INS) of adsorbed dihydrogen and Fourier-Transformed Infra-Red (FTIR) spectroscopy measurements of adsorbed CO and NO reveal that copper is encountered in two oxidation states. At least two types of Cu(I) ions are clearly detected as well as some heterogeneity of the Cu(II) species. The number of these Cu species is different in the two investigated ZSM-5 materials and depends on the Cu exchange level. With the aid of DFT model cluster calculations we find that under different coordination environments, determined by the Al distribution, both mono- and divalent Cu ions could bind H2 with a different strength. Unprecedentedly, we found that Cu-ions compensating two Al atoms, i.e. formally Cu(II) species, relatively far apart from each other, may behave very similarly to the monovalent Cu-species or alternatively viewed – as Cu(I) species that compensate for two framework Al-atoms. Such Cu-species also form stable η2 dihydrogen complexes.

Effect of Copper Addition on the AlCoCrFeNi High Entropy Alloys Properties via the Electroless Plating and Powder Metallurgy Technique

To improve the AlCoCrFeNi high entropy alloys’ (HEAs’) toughness, it was coated with different amounts of Cu then fabricated by the powder metallurgy technique. Mechanical alloying of equiatomic AlCoCrFeNi HEAs for 25 h preceded the coating process. The established powder samples were sintered at different temperatures in a vacuum furnace. The HEAs samples sintered at 950 °C exhibit the highest relative density. The AlCoCrFeNi HEAs model sample was not successfully produced by the applied method due to the low melting point of aluminum. The Al element’s problem disappeared due to encapsulating it with a copper layer during the coating process. Because the atomic radius of the copper metal (0.1278 nm) is less than the atomic radius of the aluminum metal (0.1431 nm) and nearly equal to the rest of the other elements (Co, Cr, Fe, and Ni), the crystal size powder and fabricated samples decreased by increasing the content of the Cu wt%. On the other hand, the lattice strain increased. The microstructure revealed that the complete diffusion between the different elements to form high entropy alloy material was not achieved. A dramatic decrease in the produced samples’ hardness was observed where it decreased from 403 HV at 5 wt% Cu to 191 HV at 20 wt% Cu. On the contrary, the compressive strength increased from 400.034 MPa at 5 wt% Cu to 599.527 MPa at 15 wt% Cu with a 49.86% increment. This increment in the compressive strength may be due to precipitating the copper metal on the particles’ surface in the nano-size, reducing the dislocations’ motion, increasing the stiffness of produced materials. The formability and toughness of the fabricated materials improved by increasing the copper’s content. The thermal expansion has increased gradually by increasing the Cu wt%.

Rational modification in the photochromic and self-bleaching performance of hierarchical microsphere Cu@h-WO3/WO3·nH2O composites

Herein, we used a self-assembly method to synthesize novel Cu@h-WO3/WO3·nH2O hierarchical microsphere composites with enhanced photochromism and self-bleaching performance. The composite fabricated with 1.0% Cu-WO displayed a rapid change from light-yellow to dark-gray after 2 min of ultraviolet irradiation and self-bleached in less than 1 h in the dark. Composite samples were characterized to investigate changes in their morphology and structure after being doped with different amounts of Cu. The hierarchical microspheres were composed of small, well-dispersed nanorods that provided active sites capable of absorbing light. Ensuring the proper Cu content in the WO3 lattice promoted the separation of carriers through interfacial charge transfer (IFCT) and prevented the recombination of electron-hole pairs due to excessive doping. Combing hexagonal WO3 with WO3·nH2O and Cu provided unobstructed channels, proton sources, and interactions with W species, which improved the efficiency of proton insertion and extraction. The WO3 hybrid materials described in this research displayed high coloration efficiencies and reversibility and may find applications in solar energy devices.

Copper-Doped ZnO Visible Light Photocatalyst for Degradation of Methylene Blue.

Water pollution due to uncontrolled liberation of industrial toxic chemicals, materials, drugs and dyes is one of the major causes of environmental contamination. Solar energy is one of the natural energy sources that can degrade toxic dyes in the presence of suitable active catalysts. Despite of having several advanced semiconductor-based photocatalysts, there is an open domain for the preparation of economical, cheap and high effective photocatalysts for the degradation of toxic dyes. In this study, we have prepared nanosized Cu-doped ZnO photocatalysts containing different amounts of Cu (0.1, 0.2, and 0.3 wt%) by a hydrothermal process followed by calcination at 500 °C for methylene blue (MB) degradation. The incorporation of Cu into the ZnO lattice and the crystal structure stability of the prepared catalysts are confirmed by X-ray photoelectron spectroscopy and powder X-ray diffraction. Our study shows that the photocatalytic activity of ZnO toward MB degradation under visible light can be effectively enhanced by doping it with Cu.

Copper-dependent biological effects ofparticulate matter produced by brake systems on lung alveolar cells.

Road traffic is one of the main sources of particulate emissions into the environment and has an increasing, negative impact on the release of potentially dangerous materials. Vehicle brakes release a significant amount of wear particles, and knowledge regarding their possible adverse effects is limited. One of the most dangerous elements contained in brake pads is copper (Cu), known to be toxic for human health. Therefore, our aim was to study the cell toxicity of particulate matter (PM) produced by different combinations of braking discs and pads containing different amounts of Cu. We investigated whether brake-derived microparticles have toxic effects on lung cells proportionally to their Cu content. Analyte content was measured in friction materials by XRFS and in PM2.5 captured during braking tests using SEM/EDX. The biological impact of brake-derived PM2.5 was investigated on a human epithelial alveolar cell line (A549). Cell viability, oxidative stress, mitochondrial membrane potential, apoptosis, and the pro-inflammatory response of the cells, as well as gene expression, were assessed following exposure to increasing PM2.5 concentrations (1, 10, 100, 200, and 500µg/ml). The brake debris with the lowest Cu content did not induce significant changes in biological effects on A549 cells compared to normal controls, except for ROS production and IL6 gene expression. PM2.5 containing higher Cu quantities induced cell toxicity that correlated with Cu concentration. Our data suggest that the toxicity of PM2.5 from the brake system is mainly related to Cu content, thus confirming that eliminating Cu from brake pads will be beneficial for human health in urbanized environments.

The effects of Cu, Zn and Zr on the solution temperature and quenching sensitivity of Al–Zn–Mg–Cu alloys

This study is aimed at exploring the effects of the addition of different amounts of Cu, Zn and Zr on the solution temperature and quenching sensitivity of Al–Zn–Mg–Cu alloys. The main concerns are that low solution temperature and high quenching sensitivity will bring about disturbances during the manufacture of AA7075 aluminum alloys. Therefore, overcoming these difficulties is the goal.It was observed in the experiments that when a high copper alloy was subjected to heat treatment over 530 °C, there was an obvious melting phenomenon at the grain boundaries. After reducing some of the copper, an homogenizing heat treatment led the eutectic T phase (Mg3Zn3Al2) and η phase (MgZn2) of the Al–Zn–Mg–Cu alloy to dissolve fully into the aluminum matrix rather than precipitating the low melting point's (~495 °C) S phase (Al2CuMg). This enhanced the alloy solution temperature and improved the solution treatment efficiency. Besides, by adding a certain amount of zinc to the alloy, the precipitation amount of strengthening phase η′(MgZn2) was increased. This compensated for the reduction in the mechanical strength of the alloy containing less copper. The results showed that the addition of the zinc atoms not only elevated the strength of the alloy, but also caused no damage to the ductility. Furthermore, the addition of zirconium atoms improved the quenching sensitivity of the alloy.