Effect Of Cu Ions Research Articles

Enhanced the SRB corrosion resistance of 316L stainless steel via adjusting the addition of Cu and Ce elements

316L stainless steel (SS) is the key raw material for the preparation of high-performance oil and gas pipelines, but even 316L with excellent properties will be attacked by sulfate-reducing bacteria (SRB) corrosion. Excellent antibacterial effects have been obtained in other SS systems by doping antibacterial elements. However, the current research on the preparation of antibacterial 316L SS is not comprehensive, and the quantitative analysis of the antibacterial mechanism and doping elements is still unclear. In this paper, the SS with Cu and Ce added were prepared by vacuum induction melting. Then the homogenization treatment combined with hot rolling was used to improve the structure segregation and mechanical properties. Further, the weight loss tests and electrochemical tests were conducted to evaluate the corrosion resistance of SS, the corrosion products and morphology were analysed, and the deformation structure was characterized to clarify the corrosion mechanism of the modified SS and quantify the doping elements. The results indicate that the microstructure after homogenization is mainly austenite, and with the increase of Ce content, the Ce-rich phase segregates. The inhibitory effect of Cu on SRB can be explained by the destructive effect of Cu ions on cell membranes. On this basis, adding a low content of Ce element can increase the permeability of the SRB cell wall and further enhance the attack effect of Cu ions on the cell membrane. The corrosion behavior of alloys shows the deformation structure dependence, with crystal defects and segregation increasing the corrosion rate. The optimal addition amount of Ce is 0.18 wt%, and the strength and elongation of SS are 511.18 MPa and 108.2%, respectively.

Near-infrared Ⅱ light-assisted Cu-containing porous TiO2 coating for combating implant-associated infection

Treatment implant-associated infections remains a severe challenge in the clinical practice. This work focuses on the fabrication of Cu-containing porous TiO2 coatings on titanium (Ti) by a combination of magnetron sputtering and dealloying techniques. Additionally, photothermal therapy is employed to enhance the effect of Cu ions in preventing bacterial infection. After the dealloying, most of Cu element was removed from the magnetron sputtered Cu-containing films, and porous TiO2 coatings were prepared on Ti. The formation of porous nanostructures significantly enhanced the photothermal conversion performance under NIR-II light irradiation. The combined effect of hyperthermia and Cu ions demonstrated enhanced antibacterial activity in both in vitro and in vivo experiments, and the antibacterial efficiency can reach 99% against Streptococcus mutans. Moreover, the porous TiO2 coatings also exhibited excellent biocompatibility. This modification of the titanium surface structure through dealloying changes may offer a novel approach to enhance the antimicrobial properties of titanium implants.

A Shuttle-Free Solid-State Cu-Li Battery Based on a Sandwich-Structured Electrolyte.

Cu-Li batteries leveraging the two-electron redox property of Cu can offer high energy density and low cost. However, Cu-Li batteries are plagued by limited solubility and a shuttle effect of Cu ions in traditional electrolytes, which leads to low energy density and poor cycling stability. In this work, we rationally design a solid-state sandwich electrolyte for solid-state Cu-Li batteries, in which a deep-eutectic-solvent gel with high Cu-ion solubility is devised as a Cu-ion reservoir while a ceramic Li1.4 Al0.4 Ti1.6 (PO4 )3 interlayer is used to block Cu-ion crossover. Because of the high ionic conductivity (0.55 mS cm-1 at 25 °C), wide electrochemical window (>4.5 V vs. Li+ /Li), and high Cu ion solubility of solid-state sandwich electrolyte, a solid-state Cu-Li battery demonstrates a high energy density of 1 485 Wh kgCu -1 and long-term cyclability with 97 % capacity retention over 120 cycles. The present study lays the groundwork for future research into low-cost solid-state Cu-Li batteries.

A Shuttle‐Free Solid‐State Cu−Li Battery Based on a Sandwich‐Structured Electrolyte

AbstractCu−Li batteries leveraging the two‐electron redox property of Cu can offer high energy density and low cost. However, Cu−Li batteries are plagued by limited solubility and a shuttle effect of Cu ions in traditional electrolytes, which leads to low energy density and poor cycling stability. In this work, we rationally design a solid‐state sandwich electrolyte for solid‐state Cu−Li batteries, in which a deep‐eutectic‐solvent gel with high Cu‐ion solubility is devised as a Cu‐ion reservoir while a ceramic Li1.4Al0.4Ti1.6(PO4)3 interlayer is used to block Cu‐ion crossover. Because of the high ionic conductivity (0.55 mS cm−1 at 25 °C), wide electrochemical window (>4.5 V vs. Li+/Li), and high Cu ion solubility of solid‐state sandwich electrolyte, a solid‐state Cu−Li battery demonstrates a high energy density of 1 485 Wh kgCu−1and long‐term cyclability with 97 % capacity retention over 120 cycles. The present study lays the groundwork for future research into low‐cost solid‐state Cu−Li batteries.

Cu2+ assisted Mn-doped perovskite nanocrystals thin films: Room-temperature synthesis and improved emission efficiencies

Mn and Cu co-doped perovskite nanocrystal (NCs) thin films with high Mn2+ doping concentration are successfully achieved by a simple one-pot method at room temperature. Structural and compositional analyses manifest that Cu2+ ions can partly replace the Pb2+ ions in the lattice structure and effectively reduce the defect concentration of 2 CsPb(Br/Cl)3 NCs. Steady-state and time-resolved photoluminescence (PL) spectroscopy were employed to characterize the effect of Cu ions doping on the luminescence properties of Mn-doped CsPb(Br/Cl)3 NCs. Mn2+ related PL quantum yields of Mn-doped CsPb(Br/Cl)3 NCs thin films with the Mn/Pb ratios of 7:1 was validly improved from ~34% to ~50% because of the incorporation of Cu2+ ions. Our work provides a low-cost synthesis for Mn-doped perovskite NCs thin films with high emission efficiency in the application of lighting, display and photodetector.

Effect of colloid-size copper-based pesticides and wood-preservatives against microbial activities of Gram-positive Bacillus species using five-day biochemical oxygen demand test

Copper-based pesticides and wood preservatives could end up in the environment during production, use, and end-of-life via different pathways that could cause unintended ecological and adverse health effects. This paper provides the effect of colloid-size Cu-based pesticides (CuPRO and Kocide), micronized Cu azole (MCA-1 and MCA-2) and alkaline Cu quaternary (ACQ) treated woods, Cu2+, Cu2+ spiked untreated wood (UTW), and CuCO3 solutions against Gram-positive Bacillus species using five-day biochemical oxygen demand (BOD5) standard test. The total Cu leached from MCA-1, MCA-2, and ACQ in Milli-Q water after 5 days were ~0.1, ~0.11, and ~0.64 g/kg of wood, respectively. However, the form of Cu leached from MCA woods was mostly ionic (> 90%). The total organic carbon (TOC) content of any tested wood (UTW/MCA-1/MCA-2/ACQ) was ~99% of its corresponding total carbon (TC) content, whereas the TOC of any tested wood sawdust exceeded that of its corresponding piece/block by > 300%. The dissolved oxygen (DO) consumption value in the presence of Cu2+, CuCO3, CuPRO, and Kocide solutions was significantly influenced by Cu particles/ions. However, the DO consumption value in the presence of UTW/MCA-1/MCA-2/ACQ woods was significantly influenced by organics leached from woods. On the other hand, the DO consumption of MCA sawdust was greater than (300%) that of MCA pieces/block. The findings of this study provide more insight into how organics leached from woods significantly reduce the toxic effects of Cu ions against Gram-positive Bacillus species.

Estimation of concentration of nano-sized voids ingrained in CuO doped lithium sulphophosphate amorphous system using positron annihilation spectroscopy

This study is devoted to investigate the effect of Cu ions on the concentration of defect centres like free volume elements (which influence the physical properties of the glasses to a large extent), integrated in exotic lithium magnesium sulphophosphate glasses using positron (e+) annihilation lifetime spectroscopy (PAL) technique. Glasses of a particular composition viz., 20Li2SO4–20MgO–(60-x) P2O5: xCuO (0 ≤x ≤ 1.0 in mol%) were prepared by traditional melt-quenching technique. The analysis of the glass structure by means of spectroscopic studies, indicated that there is a gradual increasing fraction of Cu+ ions with increase of CuO content. The analysis further suggested that Cu2+ ions acted as modifiers in the glass network while Cu+ ions took part network forming position and increased the rigidity of the glass network. Later, positron annihilation decay profiles in the samples were recorded. 22Na isotope (0.1 MBq) was used as the positron source for this study. The obtained decay profiles were resolved in to three components and the corresponding intensity (I) and lifetime (τ) parameters were estimated and their variations with the concentration of CuO were plotted. The plots suggested that among the three intensity components, the third component (even though its contribution to the total intensity is small) exhibited the largest lifetime and further exhibited a decreasing trend with increase of CuO content. Moreover, radius of the cavity (R) and the fraction free volume (fv) entrenched in the glass matrix are found to decrease with increase of CuO concentration. The analysis of results of these studies in combination with the conclusions drawn from dielectric and related studies suggested a gradual decreasing concentration of Oh Cu2+ ions which induce free volume defects by acting as modifiers. Overall analysis of the results of PAL studies suggested increasing content of CuO facilitates the increasing rigidity or increasing corrosion resistance of lithium sulphophosphate glasses.

Antibacterial behavior and related mechanisms of martensitic Cu-bearing stainless steel evaluated by a mixed infection model of Escherichia coli and Staphylococcus aureus in vitro

Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) are the most typical pathogenic bacteria with a significantly high risk of bio-contamination, widely existing in hospital and public places. Recent studies on antibacterial materials and the related mechanisms have attracted more interests of researchers. However, the antibacterial behavior of materials is usually evaluated separately on the single bacterial strain, which is far from the practical condition. Actually, the interaction between the polymicrobial communities can promote the growing profile of bacteria, which may weaken the antibacterial effect of materials. In this work, a 420 copper-bearing martensitic stainless steel (420CuSS) was studied with respect to its antibacterial activity and the underlying mechanism in a co-culturing infection model using both E. coli and S. aureus. Observed via plating and counting colony forming units (CFU), Cu releasing, and material characterization, 420CuSS was proved to present excellent antibacterial performance against the mixed bacteria with an approximately 99.4 % of antibacterial rate. In addition, 420CuSS could effectively inhibit the biofilm formation on its surfaces, resulting from a synergistic antibacterial effect of Cu ions, Fe ions, reactive oxygen species (ROS), and proton consumption of bacteria.

A potential strategy for in-stent restenosis: Inhibition of migration and proliferation of vascular smooth muscle cells by Cu ion.

The in-stent restenosis (ISR) often happens after the implantation of metal stents, including both bare metal stents (BMSs) and drug-eluting stents (DESs). Drug release from DESs could reduce significantly the occurrence of ISR but also suppress the revascularization and cause thrombosis. In this study, the effect of Cu ion in a range of 0 to 500μM on the migration and proliferation of rat aortic smooth muscle cells (RASMCs) was investigated by a series of in vitro experiments including wound-healing assay, cell viability assay and flow cytometric analysis. It has been found that the critical concentration of Cu ion should be at least 250μM in order to significantly inhibit the migration of RASMCs and the proliferation of RASMCs were impeded by every dose of Cu ion used in this study. In addition, the protein level of caspase-3 was upregulated by 250μM and 500μM Cu2+ exposure, which might be the main reason for RASMCs apoptosis. Thus, it is proposed that ISR might be prevented by the constant release of Cu ion.

Effect of copper nanoparticles and ions on spermatozoa motility of sea trout (Salmo trutta m. Trutta L.)

Nanoproducts are being increasingly used in various industrial products, leading to a greater risk of water pollution through their discharge into environment as production byproducts. Increased levels of environmental pollution with nanoproducts pose a threat to all living organisms. Nanopollutants may have toxic effects on gametes and fertilization process in species with external fertilization, thereby reducing effectiveness of reproduction or greatly impairing it. The objective of the present study was to determine the effect of copper nanoparticles (Cu and CuO) and copper ions (CuSO4·5H2O) on the spermatozoa motility of sea trout and compare their harmful effects.Copper nanoparticles (NPs) of primary particle size <100 nm and CuO NPs of particle size <50 nm as well as a solution of CuSO4·5H2O were used for the study. Concentration of the products tested (CuNPs, CuONPs, and CuSO4·5H2O) was expressed as mg Cu L−1 in the media regardless of dissolution and aggregation. A suspension with concentration up to 500 mg L−1 in an aquatic environment was tested. Spermatozoa motility under direct contact with copper at 10 s post activation was evaluated using an automated system (CASA).Copper products in an aqueous environment primarily cause a reduction of spermatozoa velocity (VCL). A significant reduction of velocity in CuSO4·5H2O salt solution occurred at concentration starting from 8 mg L−1, whereas in solutions containing CuNPs and CuONPs this process is observed from 50 mg L−1. Reduction of percentage of motile spermatozoa occurred in CuNPs from a concentration of 125 mg L−1, while in CuONPs and CuSO4·5H2O, the effect began at concentration from 250 mg L−1. In a solution of CuSO4·5H2O at a concentration of 500 mg L−1, strong agglutination of sperm cells occurred and movement ceased (immobilization IC100). Exposure to CuONPs decreased the motility rate to below IC50, while for CuNPs, the motility rate reached 80%. Changes in linearity (LIN) and amplitude of head displacement (ALH) differed according to Cu products. Cu as CuSO4·5H2O and CuONPs impaired the LIN, while CuNPs lowered ALH. Duration of motility increased at low CuSO4·5H2O concentration.The effect of Cu ion on sea trout spermatozoa motility was more harmful than that of copper nanoparticles. The various copper products used affected motility parameters differently. Contamination of aqueous environment with copper primarily caused reduction in male gamete velocity, which may impair reproduction. Various copper products had different effects on LIN, ALH, and motility duration, which can also affect fertilization.

Insights into the synergetic effect for enhanced UV/visible-light activated photodegradation activity via Cu-ZnO photocatalyst

A series of Cu-doped ZnO (Cu-ZnO) photocatalysts have been synthesized by a simple hydrothermal method. X-ray diffraction (XRD), UV–vis diffuse reflectance spectroscopy (UV–vis DRS), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) confirmed that Cu ions have been effectively incorporated into the ZnO lattice, and as the doped Cu amounts increased to 1.5%, the Cu2O will be formed. Under the effect of Cu ions and the Cu2O/ZnO heterojunction, the prepared 1.5% Cu-ZnO nanocomposites exhibited superior catalytic activity in photodegradation of Rhodamine B (RhB) dye under UV light irradiation. RhB could be degraded 99.9% after the irradiation time of 21 min. The photodegradation rate constant achieved 0.2429 min−1, which was 2 times than that of pure ZnO. The results of photoluminescence (PL) and photoacoustics (PA) spectroscopy studies indicated that the recombination efficiency of photogenerated electrons and holes was decreased for 1.5% Cu-ZnO nanocomposites as compared to that of samples. The surface photovoltage (SPV) and the transient photovoltage (TPV) measurements directly demonstrated that separation efficiency was improved, and the recombination time of electrons and holes in 1.5% Cu-ZnO nanocomposites was prolonged due to the synergistic effect of the impurity level and p-n heterojunction. Finally, the possible mechanism is proposed to illuminate the photogenerated charge behavior under UV light irradiation，and the roles of doped Cu and precipitated Cu2O in the photodegradation process were discussed. This work opens a novel avenue to preparing the metal doping photocatalysts with efficiently charge separation and charge transfer.

Adsorption of Cu and Ni Ions from Aqueous Solutions by Commercial Activated Carbon and the Reutilization in Glass Coloration

Toxic Cu(II) and Ni(II) ions in aqueous solutions were adsorbed by microporous activated carbon (AC). The adsorption isotherm and kinetics correlation coefficients indicate that the adsorption of Cu(II) and Ni(II) ions on the AC fits the pseudo second-order rate model and Langmuir adsorption model. The used AC adsorbents containing the adsorbed Cu and Ni ions were used as colorant in glass preparation. The coloration effect of Cu ions was influenced by the carbon absorbent included in the glass batch due to the reduction phenomenon, while the coloration of Ni ions was not affected.

Irradiation effects of Cu ions on the electrical and morphological properties of polypropylene

The irradiation of metallic ions on polymeric surfaces may change the chemical, electrical and physical properties of polymers. In this article, we have investigated the effects on the electrical and morphological properties of polypropylene caused by irradiating with copper (Cu) ions generated from laser-produced plasmas. For this purpose Nd: YAG laser (1064 nm) was employed to produce Cu ions. The flux of ions was controlled by varying the number of laser shots in the range 100–400, with a step size of 100. The changes in the electrical conductivity of the irradiated sample were studied using a four-point probe technique, while the surface features were examined by using optical microscopy. The electrical conductivity changed from 4.758 × 10−8 Ω−1 cm−1 to 5.003 × 10−8 Ω−1 cm−1 for unexposed and exposed (with 400 shots) samples, respectively.

Acute toxicity and biodistribution of different sized copper nano-particles in rats after oral administration

In order to compare the detailed toxicity of nano‑copper and CuCl2·2H2O (Cu ions) in vivo, the oral toxicity of four differently sized Cu particles (30 nm, 50 nm, 80 nm and 1 μm) on rats was investigated compared with CuCl2·2H2O in acute exposure scenarios. We compared the acute LD50 values and evaluated the kinetics of Cu following a single equivalent dose (200 mg/kg) of five Cu materials. Continuous gavage of nano‑copper for 7 days, the mortality rates, relative organ weights, and hematological, biochemical, and histopathologic characteristics of rats were examined. The results showed that the LD50 values of Cu ions, 30 nm, 50 nm, 80 nm, and 1 μm copper particles were 359.6, 1022, 1750, 2075, and >5000 mg/kg, respectively. Physiological and biochemical indexes indicated that 80 nm nano‑copper (Cu NPs) produced the highest degrees of toxicity in short term. The liver and kidneys were the major organs most affected by Cu NPs, and also the target organs for Cu accumulation. The toxic effects of Cu ions are similar to those of nano‑copper, but they were not the same. Therefore, the toxic effect of nano‑copper is likely to be the result of the dual action of nano‑copper particles and copper ions. Collectively, the acute toxic effects produced by Cu NPs were highly correlated with particle size. Moreover, the toxic effects produced by repeated dosing differed from those produced by a single dose, and this may be due to organ targeting effects that are dependent on the size of the nano-particles.

Effect of copper ions on the mercury re-emission in a simulated wet scrubber

In recent years, Hg re-emission from the wet scrubber has become a hot topic in the field of Hg abatement since wet scrubber has been considered as an effective way to remove Hg. In this paper, the effects of Cu ions on Hg re-emission were investigated for the first time in the presence of SO32−. The effect of CuCl32− was proved to directly reduce Hg2+ to insoluble Hg0 and to catalytically decompose Hg(SO3)22− to Hg0 and SO42− in the presence of SO32−. When adding the Cu2+ into solution with low concentration, Hg re-emission was increased due to the generation of Cu+ from the reduction of Cu2+ by SO32−. Further increase of Cu2+ concentration inhibited Hg re-emission, which was possibly owing to the formation of metal Cu which could absorb Hg0 to form amalgam. The decomposition of Hg(SO3)22− by CuCl32− and Cu+ meet pseudo-first-order reaction with respect to Hg0 and the activation energy parameters are 64.43 and 48.78kJ/mol, respectively. Difference of electron transfer path in the decomposition of Hg(SO3)22− with Cu+ was proposed to be the reason of low activation energy.

Copper Coordination Features of Human Islet Amyloid Polypeptide: The Type 2 Diabetes Peptide.

Human islet amyloid polypeptide (hIAPP) is the major component of amyloid deposits found in pancreatic β-cells of patients with type 2 diabetes (T2D). Copper ions have an inhibitory effect on the amyloid aggregation of hIAPP, and they may play a role in the etiology of T2D. However, deeper knowledge of the structural details of the copper-hIAPP interaction is required to understand the molecular mechanisms involved. Here, we performed a spectroscopic study of Cu(II) binding to hIAPP and several variants, using electron paramagnetic resonance (EPR), nuclear magnetic resonance (NMR), electronic absorption, and circular dichroism (CD) in the UV-vis region in combination with Born-Oppenheimer molecular dynamics (BOMD) and density functional theory geometry optimizations. We find that Cu(II) binds to the imidazole N1 of His18, the deprotonated amides of Ser19 and Ser20, and an oxygen-based ligand provided by Ser20, either via its hydroxyl group or its backbone carbonyl, while Asn22 might also play a role as an axial ligand. Ser20 plays a crucial role in stabilizing Cu(II) coordination toward the C-terminal, providing a potential link between the S20G mutation associated with early onset of T2D, its impact in Cu binding properties, and hIAPP amyloid aggregation. Our study defines the nature of the coordination environment in the Cu(II)-hIAPP complex, revealing that the amino acid residues involved in metal ion binding are also key residues for the formation of β-sheet structures and amyloid fibrils. Cu(II) binding to hIAPP may lead to the coexistence of more than one coordination mode, which in turn could favor different sets of Cu-induced conformational ensembles. Cu-induced hIAPP conformers would display a higher energetic barrier to form amyloid fibrils, hence explaining the inhibitory effect of Cu ions in hIAPP aggregation. Overall, this study provides further structural insights into the bioinorganic chemistry of T2D.

Effect of Cu ions assisted conductive filament on resistive switching memory behaviors in ZnFe2O4-based devices

Resistive random access memory (RRAM) has been developing as a most promising non-volatile memory in the current memory technology. In this work, ZnFe2O4 (ZFO) nano powder were firstly prepared by co-precipitation assisted hydrothermal process. Further, the resistive switching memory devices with Ag/Cu doped ZnFe2O4 (CZFO)/Au/Si and Ag/ZFO/Au/Si structures grown on silicon (Si) substrate were prepared by radio frequency magnetron sputtering, and their memory behaviors were contrastively investigated. It is observed the Cu doping can obviously affect the bipolar resistive switching memory characteristics. Thus a model concerning the formation and rupture of Cu ions assisted conductive filament inside the CZFO layer is suggested to explain the change of memory behaviors. These works provide a foundation for exploring the memory application of multifunctional material and further regulate their nonvolatile memory behaviors.

Investigations of copper sulfide diffusion into paper insulation of transformers

It is well established that copper sulfide is formed due to reaction of sulfur with copper conductors in transformers and reactors. However, there is very little experimental evidence to demonstrate copper sulfide diffusion into bulk of paper. Diffusion experiments have been carried out on three samples of kraft paper having different thickness. Positron Annihilation Lifetime Spectroscopy has been used to investigate the possibilities of copper sulfide diffusion into bulk of paper. This study has demonstrated that copper sulfide can diffuse into the bulk of paper leading to either increase or decrease in free volume of paper. The reasons for changes in free volume of paper due to copper sulfide deposits are explained. The consequences of copper sulfide diffusion on PD, voltage-current characteristics under ac and volume resistivity are discussed. Electric field simulation has been used to explain the effects of Cu ions and copper sulfide formation on electric stress distribution across paper.

ANTIMICROBIAL ACTIVITY OF COPPER KAOLINITE AND SURFACTANT MODIFIED COPPER KAOLINITE AGAINST GRAM POSITIVE AND GRAM NEGATIVE BACTERIA

The aim of this research was to determine the antimicrobial activity of kaolinite modified with antimicrobial compounds against Gram positive and Gram negative bacteria. Copper kaolinite (Cu-kaolinite) was prepared by loading raw kaolinite with copper nitrate trihydrate (CuNO3) while surfactant modified Cu-kaolinite (SM-Cu-kaolinite) was prepared by adding cationic surfactants hexadecyltrimethyl ammonium (HDTMA) on Cu-Kaolinite. Samples was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) analyzer. The antimicrobial activity of the samples was tested against Gram negative bacteria (Escherichia coli ATCC 11229 and Pseudomonas aeruginosa ATCC 15442), and Gram positive bacteria (Staphylococcus aureus ATCC 6538 and Enterococcus faecalis ATCC 29212) through disc diffusion technique (DDT) and minimum inhibition concentration (MIC). The results showed that the antimicrobial activity of Cu-kaolinite increased after modified with HDTMA due to the synergistic effects of Cu ions and HDTMA molecules on the kaolinite. The antimicrobial activity for surfactant modified Cu-kaolinite was greater for Gram positive bacteria compared to Gram negative bacteria. In conclusion, the attachment of HDTMA on Cu-kaolinite contributed to the enhanced antimicrobial activity against wide spectrum of bacteria (Gram positive and Gram negative bacteria).

Mechanical and Structural Properties of Zinc – Sodium - Phosphate Glasses Doped with Cu&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;O

Ternary Zinc-Sodium-Phosphate glasses doped with copper of the composition 40ZnO-(20-x) Na₂O-40P₂O₅-xCu₂O where x =0, 2, 4, 6, 8 mol % were prepared by the tradition quenching method. The effect of Cu ions on density, molar volume and microhardness has been investigated. FTIR was measured in the range (400-1600) cm-1 to investigate the effect of Cu ion on the structure of the studied glass. Longitudinal and shear velocities were measured for the studied glass using pulse echo technique. Elastic properties such as longitudinal modulus, shear modulus, bulk modulus, and Young’s modulus, Poisson’s ratio) and some physical parameters such as softening temperature, hardness, Debye temperature have been calculated. The ultrasonic results and the other measured parameters indicate the Cu ion increase the cross-link density by the formation of P-O-Cu. All the measurements are measured at room temperature.