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At least 1,153 records · Page 64

The Characterization of Dissolved Organic Matter in Reclaimed Water and Its Influence on Copper Toxicity

Water samples were collected from five phases of treatment in a municipal sewage reclaimed water plant and the DOM was characterized. Results indicated that the components and properties of DOM varied notably with sequential treatments, such as the fluorescence intensity, the molecular weight and the total acidity. Meanwhile the accumulation of Cu in Daphnia magna was analyzed following exposure to samples spiked with 50 µg/L copper, which were decreased by the presence of DOM in those water samples. Furthermore, this study found significant associations between fluorescence intensity and Cu accumulation (r{sup 2} = 0.778, p < 0.05), while increased total acidity was found to enhance the unit total organic carbon-Cu accumulation (r{sup 2} = 0.979, p < 0.01). This study provides useful information on the safety and effective management of reclaimed water as a potential water resource.

54 ENVIRONMENTAL SCIENCES↗

Development of a New 4-Amino-1,8-Naphthalimide Derivative as a Fluorescent Probe for Monitoring the Divalent Copper Ion

This article presents the design and synthesis of a new variant of the 4-amino-1,8-naphthalimide fluorescent probe for monitoring the divalent copper ion, Cu{sup 2+}. The probe BRST, functionalized with two propionic carboxylic acid groups in its receptor moiety, demonstrated high selectivity and sensitivity for the detection of Cu{sup 2+} in competitive media of various metal ions in DMSO/HEPES buffer solution (1:1; pH 7.4), with a fluorescence quenching of 75.41%. Besides its good linearity with Cu{sup 2+}, the probe yielded commendable values of the association constant and the detection limit, 5.54 × 10{sup 5} M{sup –1} and 4.33 × 10{sup –9} M, respectively. The quenching of the fluorescence intensity of the sensor in the presence of Cu{sup 2+} ions is attributable to the strong paramagnetic nature of the Cu{sup 2+} ion. The fluorescence 'turn off' behavior of this simple and effective probe was successfully applied for the determination of Cu{sup 2+} levels in untreated water samples, with excellent recovery rates of 98–105.8%.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Removal of Iron and Copper Ions from the Liquid Phase by Modified Polymeric Membranes

Preparation of polymeric membranes based on cellulose acetate and modified by adding different amounts of a pore generating agent, which was polyvinylpyrrolidone (PVP), is presented and potential application of the membranes obtained for the removal of iron and copper ions from liquid phase is examined. Addition of various amounts of PVP has an impact on the physical (porosity, equilibrium water content and permeability) and chemical (content of the surface oxygen group, pH) properties of the membranes obtained. Filtration of iron and cupper solution leads to significant changes in the total content of surface oxygen groups, however the acidic oxygen groups remain dominant. With the content of PVP increasing within a certain range, the membrane permeability is improved. The membranes obtained show higher efficiency in removal of Fe{sup 3+} than Cu{sup 2+} ions, but with increasing content of PVP the efficiency in iron ions removal decreases and the total filtration resistance decreases after filtration of iron ions solutions.

36 MATERIALS SCIENCE↗

Chitosan Functionalization with Amino Acids Yields to Higher Copper Ions Adsorption Capacity

Chitosan (Chi) beads were conjugated with three different amino acids [namely, glutamic acid (GLU), methionine (MET), and taurine (TAU)] aiming to increase the divalent copper ions uptake in aqueous media. Scanning Electron Microscopy evidenced the development of a large porous structure after amino acid functionalization, associated with the increase in a number of amino groups in the polymer backbone. X-Ray Photoelectron Spectroscopy and Fourier-Transform Infrared Spectra analyses were also employed to assess the conjugation of these three different amino acids in chitosan backbone. Adsorption experiments were conducted in a batch process, at 298 K, and kinetic data indicated a slightly better fitting for the pseudo-first-order model when compared to pseudo-second order. Intraparticle diffusion model suggested a three-step mechanism for Cu(II) adsorption kinetics, limited by the third step, the intraparticle diffusion. The isotherm data fitting to the traditional Langmuir and Freundlich models indicated a better fit for the former case. The amino acid conjugation resulted in the increase of the maximum adsorption capacity for Cu(II) from 1.30 mmol g{sup −1} prior to amino acid conjugation to values as high as 2.31 mmol g{sup −1}, 2.40 mmol g{sup −1} and 2.68 mmol g{sup −1} for Chi–TAU, Chi–GLU, and Chi–MET, respectively. These results are attributed to the introduction of additional amino groups and new carboxylate and amino acid residues into the chitosan backbone, which might also be explored for amino acid demanding applications.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Twin-core sunflower-type photonic quasicrystal fibers incorporated gold, silver, and copper microwire: an ultrashort and broad bandwidth polarization splitter

Polarization splitters are beneficial in the field of passive optical devices which are principally used in the coherent optical communication systems. An ideal polarization splitter must possess an efficient coupling with significant optical bandwidth. Hence, we proposed a novel metal-filled polarization splitter based on twin-core sunflower-type photonic quasicrystal fiber (PQF). The characteristics of the proposed splitter such as coupling length, extinction ratio, and available optical bandwidth were investigated by using the commercially available software, COMSOL Multiphysics. These aforementioned characteristics were determined by optimizing the geometrical parameters of proposed PQF—first by using gold-filled PQF (AuPQF). With optimized geometrical parameters, the splitter achieved an ultra-short coupling length of 132 µm and an ultra-broad bandwidth of 301 nm (wavelength range 1.36–1.68 µm) with an extinction ratio below than − 20 dB which comprised E + S+C + L+U band. Secondly, a comparative study to use silver- and copper-filled PQF (AgPQF and CuPQF) was explored. Both AgPQF and CuPQF retained a short length with adequate bandwidth and a significant extinction ratio below than − 20 dB. The AgPQF has a coupling length of 137 µm with a bandwidth of 136 nm which operated at 1.44 µm wavelength, while CuPQF with 134 µm lengths with a bandwidth of 149 nm and operated at 1.50 µm wavelengths.

36 MATERIALS SCIENCE↗

Structure Amorphization and Mechanical Properties of Nanolaminates of the Copper–Niobium System During High-Pressure Torsion

The results of investigation of structural transformations and mechanical behavior of nanolaminates are reported, which were manufactured by multiple rolling of alternating layers of copper and niobium, followed by high-pressure torsion in the Bridgeman chamber. A detailed analysis of structure alteration of the material under study is performed by the high-resolution TEM methods. The changes in the value of microhardness in three dimensions (3D) are investigated during variation of the degree of straining of nanolaminates in the course of their torsion. A phenomenon of structure amorphization and a sharp increase in strength characteristics are revealed.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Structural Modification of Graphene on Copper Substrates Irradiated by Nanosecond High-Intensity Ion Beams

Interaction of a nanosecond high-intensity pulsed ion beam with thin graphene films on copper substrates is analyzed. Methods of Raman spectroscopy are used to investigate the degree of graphene degradation depending on the integral implanted dose. The role of the substrate in the structural degradation of graphene irradiated by charged particle beams is demonstrated using the software package SRIM, intended for modeling radiative defect cascades under irradiation by charged particle beams, and the data on radiation resistance of graphene available in the literature.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

In-Situ X-Ray Diffraction Observations of Low Temperature Ag-Nanoink Sintering and High Temperature Eutectic Reaction with Copper

Nanoinks, which contain nm sized metallic particles suspended in an organic dispersant fluid, are finding numerous microelectronic applications. Nanoinks sinter at much lower temperatures than bulk metals due to their high surface area to volume ratio and small radius of curvature, which reduces their melting points significantly below their bulk values. The unusually low melting and sintering temperatures have unique potential for materials joining since their melting points increase dramatically after initial sintering. In this paper Ag nanoink is studied using in-situ synchrotron based x-ray diffraction to follow the kinetics of the initial sintering step by analysis of diffraction patterns, and to directly observe the high remelt temperature of sintered nanoinks. Ag nanoink is further explored as a possible eutectic bonding medium with copper by tracking phase transformations to high temperatures where melting occurs at the Ag-Cu eutectic temperature, demonstrating nanoinks as a viable eutectic bonding medium.

36 MATERIALS SCIENCE↗

Experimentally Determined Phase Diagram for the Barium Sulfide-Copper(I) Sulfide System Above 873 K (600 °C)

The phase diagram of the barium sulfide-copper(I) sulfide system was investigated above 873 K (600 °C) using a custom-built differential thermal analysis (DTA) apparatus. The melting point of barium sulfide was determined utilizing a floating zone furnace. Four new compounds, Ba{sub 2}Cu{sub 14}S{sub 9}, Ba{sub 2}Cu{sub 2}S{sub 3}, Ba{sub 5}Cu{sub 4}S{sub 7}, and Ba{sub 9}Cu{sub 2}S{sub 10}, were identified through quench experiments analyzed with wavelength dispersive X-ray spectroscopy (WDS) and energy dispersive X-ray analysis (EDS). A miscibility gap was observed between 72 and 92 mol pct BaS using both DTA experiments and in situ melts observation in a floating zone furnace. A monotectic was observed at 94.5 mol pct BaS and 1288 K (1015 °C).

36 MATERIALS SCIENCE↗

Advanced Process Possibilities in Friction Crush Welding of Aluminum, Steel, and Copper by Using an Additional Wire

Joining sheet metal can be problematic using traditional friction welding techniques. Friction crush welding (FCW) offers a high speed process which requires a simple edge preparation and can be applied to out-of-plane geometries. In this work, an implementation of FCW was employed using an additional wire to weld sheets of EN AW5754 H22, DC01, and Cu-DHP. The joint is formed by bringing together two sheet metal parts, introducing a wire into the weld zone and employing a rotating disk which is subject to an external force. The requirements of the welding preparation and the fundamental process variables are shown. Thermal measurements were taken which give evidence about the maximum temperature in the welding center and the temperature in the periphery of the sheet metals being joined. The high welding speed along with a relatively low heat input results in a minimal distortion of the sheet metal and marginal metallurgical changes in the parent material. In the steel specimens, this FCW implementation produces a fine grain microstructure, enhancing mechanical properties in the region of the weld. Aluminum and copper produced mean bond strengths of 77 and 69 pct to that of the parent material, respectively, whilst the steel demonstrated a strength of 98 pct. Using a wire offers the opportunity to use a higher-alloyed additional material and to precisely adjust the additional material volume appropriate for a given material alignment and thickness.

36 MATERIALS SCIENCE↗

Evolution of Size and Chemical Composition of Copper Concentrate Particles Oxidized Under Simulated Flash Smelting Conditions

An experimental study was conducted to elucidate the evolution of size and chemical composition of La Caridad copper concentrate particles during oxidation under simulated flash smelting conditions. Input variables tested included particle size and oxygen concentration in the process gas. The response variables included the size distributions, chemical composition, and morphology of the reacted particles at seven locations along a laboratory reactor. Particles with initial size < 45 µm contained mostly chalcopyrite, they increased their mean size and decreased the amount of dust in the population during oxidation. This was explained by a reaction path involving rapid melting followed by collision and coalescence of reacting droplets during flight. Particles with sizes > 45 µm contained varying amounts of chalcopyrite and pyrite, and tended to either maintain or decrease their mean size upon oxidation. When size reduction was observed, dust was produced because of fragmentation, and the particles showed no evidence of collisions during flight. The main oxidation products detected in the particles consisted of matte, cuprospinel, and magnetite. A plot of the mean size divided by the mean size in the feed against the fraction of sulfur eliminated generalized the experimental data so far reported in the literature, and helped identify the reaction path followed by the particles.

36 MATERIALS SCIENCE↗

Exploring As-Cast PbCaSn-Mg Anodes for Improved Performance in Copper Electrowinning

Lead calcium tin (PbCaSn) alloys are the common anodes used in copper electrowinning (Cu EW). Given a large amount of energy consumed in Cu EW process, anodes with controlled oxygen evolution reaction (OER) kinetics and a lower OER overpotential are advantageous for reducing the energy consumption. To date, magnesium (Mg) has never been studied as an alloying element for EW anodes. As-cast PbCaSn anodes with the addition of Mg were examined herein, revealing an improved performance compared to that of the industrial standard PbCaSn anode. The alloy performances in the early stages of anode life and passivation were established from electrochemical studies which were designed to simulate industrial Cu EW process. The 24-hour polarization testing revealed that the Mg alloying depolarizes the anode potential up to 80 mV; thus, resulting in a higher Cu EW efficiency. In addition, scanning electron microscopy and X-ray photoelectron spectroscopy revealed that the alteration of the alloy microstructure and the corresponding interfacial reactions contribute to the changes of the anode electrochemical performances. The present study reveals for the first time the potency of Mg alloying in reducing the overpotential of PbCaSn anode.

36 MATERIALS SCIENCE↗

Compositional and Thermal Characterization of Potential Nano-Carbon Copper Composite

Covetic materials have been claimed to be new types of metal matrix nano-composite materials. These materials are formed from face-centered-cubic metals which are alleged to be super-saturated with up to ~ 10 wt pct of activated nano-carbon. The focus of this study was to characterize the chemical composition of copper covetic materials of varying nano-carbon concentrations, and characterize the thermal properties of these materials in order to determine if these materials exhibit enhanced material properties.

36 MATERIALS SCIENCE↗

Study of the Influence of Xanthate Derivative Structures on Copper Sulfide Mineral Adsorption Under Acidic Conditions

Adsorption of commercial xanthate derivatives on copper sulfide mineral (covellite, CuS) was studied by kinetics and isotherm adsorption experiments. The adsorption of xanthate derivatives was confirmed by FTIR (Fourier transform infrared spectroscopy) and XPS (X-ray photoelectron spectroscopy) results. Experiments were performed with two different xanthate derivatives, C-4410 (O-pentyl S-2-propenyl ester) and C-4940 (isobutyl xanthogen ethyl formate), on individual doses of 0.05 g of powdered covellite. It was found that the equilibrium times at pH 2, 4, and 6 were different for both xanthate derivatives. The shortest times were achieved at pH 2 and 4. The results suggest that C-4110 can be used as collector in a wide range of pH, while C-4940 is limited to lower pH values. Pseudo first- and pseudo second-order kinetics models were thus applied to the experimental data for pH 2. The information obtained from the kinetics models combined with XPS allowed proposing the adsorption mechanism for the covellite-xanthate derivative pair. The adsorption takes place through a non-covalent interaction for C-4410 and chemisorption process for C-4940. The best-fitting isotherm models for C-4410 and C-4940 adsorption were Redlich–Peterson and Freundlich, respectively, which yield a maximum adsorption capacity of 57.07 mg g{sup −1} for C-4410 and 44.62 mg g{sup −1} for C-4940.

36 MATERIALS SCIENCE↗

Accelerated Oxygen Mass Transfer in Copper and Vanadium Oxide-Based MIEC-Redox Membrane

Mixed ionic-electronic conducting (MIEC) membranes have a great potential for use in gas separation technology in the production of pure oxygen for metallurgy, micro- and nanoelectronics, biotechnology, pharmaceutics, etc. Before this happens, an important issue has to be addressed. This issue involves the design of novel MIEC membranes with enhanced oxygen transport. Recently, a concept of thick two-layer solid/liquid composite MIEC-Redox membranes with accelerated diffusion-bubbling oxygen transfer was proposed (see Belousov and Fedorov in ACS Appl Mater Interfaces 10:21794–21798, 2018). These diffusion-bubbling membranes could serve for efficient oxygen separation from air. However, there is no enough fundamental understanding of the mass transport processes involved. This understanding is important for evaluating the potential of MIEC-Redox membranes for practical application. The presented article gives a theory of oxygen mass transfer in two-layer copper and vanadium oxide-based MIEC-Redox membranes. The theory describes both the transport of oxygen ions in the outer layer of the membrane and the nucleation, growth, and transport of oxygen gas bubbles in the inner layer of the membrane. Kinetic regularities of oxygen mass transfer are established. The ways to enhance the productivity of MIEC-Redox membranes are outlined.

36 MATERIALS SCIENCE↗

Microstructure Evolution and Failure Analysis of an Aluminum–Copper Cathode Conductive Head Produced by Explosive Welding

In this paper, microstructure evolution and failure analysis of the aluminum-copper interface of cathode conductive heads during their use were studied. The interface morphologies, compositions, conductivity and mechanical properties were investigated and analyzed. Obvious corrosion was found on the surface of the contact interface, which was more prevalent on an Al matrix. The crack increased sharply in the local metallurgical bonding areas on the interface, with the compound volume having no significant change. The phase transformation occurred on the interface during use, which was investigated using the elemental composition and x-ray diffraction pattern. The microhardness near the interface increased accordingly. An obvious electrical conductivity decrease appeared on the Al/Cu interface of the cathode conductive head after use over a specific time interval. Therefore, the deterioration of the microstructures and corrosion are the primary factors that affect the electrical conductivity and effective bonding, which will lead to eventual failure.

36 MATERIALS SCIENCE↗

Fiber Laser Welding–Brazing Characteristics of Dissimilar Metals AZ31B Mg Alloys to Copper with Mg-Based Filler

Fiber laser welding–brazing of 1-mm-thick AZ31B Mg alloys to 1.5-mm-thick copper (T2) with Mg-based filler was performed in a lap configuration. The weld appearance, interfacial microstructure and mechanical properties were investigated with different heat inputs. The results indicated that processing windows for optimizing appropriate welding parameters were relatively narrow in this case. Visually acceptable joints with certain strength were achieved at appropriate welding parameters. The maximum tensile-shear fracture load of laser-welded-brazed Mg/Cu joint could reach 1730 N at the laser power of 1200 W, representing 64.1% joint efficiency relative to AZ31Mg base metal. The eutectic structure (α-Mg + Mg{sub 2}Cu) and Mg-Cu intermetallic compound was observed at the Mg/Cu interface, and Mg-Al-Cu ternary intermetallic compound were identified between intermetallics and eutectic structure at high heat input. All the joints fractured at the Mg-Cu interface. However, the fracture mode was found to differ. For laser power of 1200 W, the surface was characterized by tearing edge, while that with poor joint strength was almost dominated by smooth surface or flat tear pattern.

36 MATERIALS SCIENCE↗

Design and Performance Evaluation of Al{sub 2}O{sub 3}-SiC Composite for Direct-Bonded Copper Substrate

A computational material design approach is applied to propose a novel ceramic material for direct-bonded copper (DBC) substrate with enhanced thermal and structural performance. The material design inherently consists of many competing requirements that require careful decisions regarding key trade-offs in terms of material composition, inclusion size, shape, and distribution to achieve the target properties. The alumina-silicon (Al{sub 2}O{sub 3}-SiC) composite, as compared to commercial alumina, used in DBC is found to be the most suitable design among other candidates with improved thermal and structural properties. In order to study the performance characteristics and the effects of the new ceramic composite with improved properties in terms of structural behavior and fatigue life of the DBC substrate, the normal working and extreme thermal cycling conditions were simulated and analyzed using finite element method. The temperature, strain, and localized stress distribution within the substrate at a steady-state condition were analyzed, and the improved Coffin–Manson law was used to calculate the fatigue life of the substrate under extreme thermal cycling conditions. The proposed Al{sub 2}O{sub 3}-SiC composite is found to be more robust than the commercial alumina as DBC substrates considering the thermal–mechanical performance. The fatigue life cycle of the DBC substrate with the proposed material is predicted to be about two times longer than the commercial alumina DBC ceramic under transient thermal cycling test.

36 MATERIALS SCIENCE↗