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At least 721 records · Page 40

Optical Properties of CdS Nanocrystals Doped with Zinc and Copper

Cadmium-sulfide nanocrystals are produced by the colloidal method. Doping with zinc and copper is conducted during nanocrystal growth. The optical absorption and photoluminescence spectra are studied. The maximum concentration of the optically active copper impurity is determined from a shift of the fundamental absorption edge to lower energies. It is shown that the long-wavelength luminescence of CdS and CdS:Zn nanocrystals is defined by optical transitions at donor–acceptor pairs. In CdS:Cu nanocrystals, optical absorption and photoluminescence in the visible spectral region are defined by recombination transitions involving the ground state of Cu{sub Zn}{sup 2+} ions. The infrared absorption and photoluminescence of CdS:Cu quantum dots are defined by intracenter transitions within Cu{sub Zn}{sup 2+} ions.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Copper Complexes with Diazoolefin Ligands and their Photochemical Conversion into Alkenylidene Complexes

Homometallic copper complexes with alkenylidene ligands are discussed as intermediates in catalysis but the isolation of such complexes has remained elusive. Herein, we report the structural characterization of copper complexes with bridging and terminal alkenylidene ligands. The compounds were obtained by irradiation of CuI complexes with N-heterocyclic diazoolefin ligands. Furthermore, the complex with a terminal alkenylidene ligand required isolation in a crystalline matrix, and its structural characterization was enabled by in crystallo photolysis at low temperature.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Structural, Electronic, and Photophysical Insights into a Few Atom Copper-Sulfur Cluster in the Solid and Solution States

Coinage-metal chalcogenide clusters are widely studied for their attractive photoluminescence properties. Copper chalcogenides are especially promising, but are often confined to solid-state investigations due to their limited solution stability and the difficulty of synthesizing stable, well-defined clusters. Here, we investigate copper–sulfur clusters incorporating a small number of Cu atoms to elucidate fundamental atomic interactions, ground- and excited-state characteristics, and photophysical behavior in both solid and solution. We have synthesized the Cu6(4,6-dimethyl-2-mercaptopyrimidine)6 cluster in both neutral and charged states, Cu6 and Cu6-2H2+, respectively, by selective ligand protonation. The molecular structures are determined using single-crystal X-ray diffraction, while Cu K-edge X-ray absorption spectroscopy is used to probe Cu electronic structure differences arising from the ligand modification. Steady-state and pump-probe optical spectroscopy is used to investigate photophysical properties, interpreted using density functional theory methods. Both clusters exhibit good stability in the solid state and in solution and show characteristic near-infrared emission with microsecond lifetimes. Overall, the Cu6S6 clusters display favorable charge–transfer characteristics and show potential for further use in driving photochemical transformations.

Copper-sulfur clusters↗

Copper Tantalate by a Sodium-Driven Flux-Mediated Synthesis for Photoelectrochemical CO 2 Reduction

Copper-tantalate, Cu 2 Ta 4 O 11 (CTO), shows significant promise as an efficient photocathode for multi-carbon compounds (C 2+ ) production through photoelectrochemical (PEC) CO 2 reduction, owing to its suitable energy bands and catalytic surface. However, synthesizing CTO poses a significant challenge due to its metastable nature and thermal instability. In this study, this challenge is addressed by employing a flux-mediated synthesis technique using a sodium-based flux to create sodium-doped CTO (Na-CTO) thin films, providing enhanced nucleation and stabilization for the CTO phase. To evaluate the PEC performance and catalytic properties of the films, copper(II) oxide (CuO) at the Na-CTO surface is selectively etched. The etched Na-CTO shows a lower dark current, with decreased contribution from photocorrosion, unlike the non-etched Na-CTO which has remaining CuO on the surface. Furthermore, Na-CTO exhibits 7.3-fold ethylene selectivity over hydrogen, thus highlighting its promising potential as a photocathode for C 2+ production through PEC CO 2 reduction.

copper tantalate↗

Catalytic Aquathermolysis of High-Viscosity Oil Using Iron, Cobalt, and Copper Tallates

The results of a study of the composition of active forms of the catalyst formed upon degradation of the precursor, based on the results of physical modeling of a sample of high-viscosity oil having high asphaltene and resin contents, are presented. Oil-soluble iron, cobalt, and copper tallates were used as the objects of the study. The composition of the separated powder of the active form of the catalyst was determined by X-ray diffraction analysis, and the catalyst particle size was determined by scanning electron microscopy. The SARA (saturate, aromatic, resin and asphaltene) analysis data revealed a marked decrease in high-molecular-weight oil components due to thermocatalytic cracking. The basic transformation mechanism is breakdown of the high-molecular-weight compounds along the sulfur-bearing bonds, as indicated by elemental CHNS (carbon, hydrogen, nitrogen and sulfur) analysis data. It is shown that the cobalt- and copper-based oil-soluble complexes turn are converted to sulfide forms and the iron-based complex is converted to the oxide form. According to the results of scanning electron microscopic analysis of the catalyst, the particle size is about 60 nm.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Structural and Optical Study of Copper-Doped Zinc Sulfide Nanoparticles

Copper-doped zinc sulfide nanoparticles have been synthesized using a wet chemical method. The synthesized nanoparticles exhibit a zinc blende structure with the crystallite size of 3.8 nm. The morphological and optical studies of the synthesized nanoparticles have been performed. It is found that the band gap varies from 3.6 to 4.4 eV depending upon the concentration of copper. The room temperature photoluminescence of the synthesized nanoparticles has been also investigated.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Ferrocene-containing tri- and tetranuclear cyclic copper(I) and silver(I) pyrazolates

New tri- and tetranuclear macrocyclic silver(I) and copper(I) 3-ferrocenyl-5-(trifluoromethyl)pyrazolates were prepared: [{(3-((η"5-C_5H_4)Fe(η"5-C_5H_5))-5-(CF_3)-Pz}M]{sub 3} (M = Cu (1), Ag (2)) and [{(3-(( η"5-C_5H_4)Fe(η"5-C_5H_5))-5-(CF_3)-Pz}Cu]{sub 4} (3). The structures of compounds were established by X-ray diffraction analysis. In the crystalline state, a planar trinuclear silver-containing macrocycliс pyrazolate and a saddle-shaped tetranuclear copper-containing macrocycle are formed. The introduction of a bulky substituent, ferrocene, into the pyrazole ligand results in complete shielding of the acidic metal sites, which precludes the coordination of base molecules.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Three-dimensional copper(II) carboxylates based on 4,4′,4″-benzene-1,3,5-triyltris(benzoic acid)

The homochiral coordination polymers [Cu{sub 4}(CH{sub 3}OH)(H{sub 2}O){sub 4}(Hbtb)(S-mal){sub 2}]•4H{sub 2}O and [Cu{sub 4}(CH{sub 3}OH)(H{sub 2}O){sub 4}(Hbtb)(R-mal){sub 2}]•4H{sub 2}O were synthesized by heating S- or R-malic acid (H{sub 3}mal), 4,4′,4″-benzene-1,3,5-triyltris(benzoic acid) (H{sub 3}btb), and copper(II) acetate in an aqueous methanolic solution. The reaction with copper(II) nitrate in aqueous dioxane afforded the coordination framework [Cu{sub 6}(C{sub 4}H{sub 8}O{sub 2}){sub 3}(H{sub 2}O){sub 3}(btb){sub 4}]•4C{sub 4}H{sub 8}O{sub 2}•10H{sub 2}O, which does not contain chiral ligands. The compositions and crystal structures of the new compounds were determined by single-crystal X-ray diffraction and confirmed by X-ray powder diffraction, IR spectroscopy, thermogravimetric and elemental analysis.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

The Effect of Deposit Temperature on the Catalytic SO{sub 2}-to-SO{sub 3} Conversion in a Copper Flash Smelting Heat Recovery Boiler

The aim of the work was to study the catalytic role of copper flash smelter deposit in the SO{sub 2}-to-SO{sub 3} conversion. In addition, the effect of process gas temperature at 548 K to 1173 K (275 °C to 900 °C) on the amount of SO{sub 3} formed was addressed both in the absence and presence of genuine copper flash smelter deposit. The SO{sub 3} conversion rate changed as a function of process gas temperature, peaking at 1023 K (750 °C). A dramatic increase in the SO{sub 2}-to-SO{sub 3} conversion was observed when process dust was present, clearly indicating that process dust catalyzes the SO{sub 2}-to-SO{sub 3} conversion. Based on these results, the catalytic ability of the deposit may lead to sulfuric acid dew point corrosion.

36 MATERIALS SCIENCE↗

Leaching Studies for Copper and Solder Alloy Recovery from Shredded Particles of Waste Printed Circuit Boards

Printed circuit boards (PCBs) comprise various metals such as Cu, Sn, and Pb, as well as platinum group metals. The recovery of metals from PCBs is important not only due to the waste treatment but also for recycling of valuable metals. In the present work, the leaching process of Cu, Sn, and Pb from PCBs was studied using fluoroboric acid and hydrogen peroxide as the leaching agent and oxidant, respectively. Pertinent factors including concentration of acid, temperature, liquid-solid ratio, and concentration of oxidizing agent were evaluated. The results showed 99 pct of copper and 90 pct solder alloy were dissolved at a temperature of 298 K (25 °C) for 180 minutes using 0.6 M HBF{sub 4} for the particle size range of 0.15 to 0.4 mm. Moreover, solid/liquid ratio had insignificant effect on the recovery of metals. Kinetics analysis revealed that the chemical control regime governs the process with activation energy 41.25 and 38.9 kJ/mol for copper and lead leaching reactions, respectively.

36 MATERIALS SCIENCE↗

Efficient Recovery of Copper and Cobalt from the Matte–Slag Mixture of ISA Furnace by Injection of Coke and Pyrite

During ISA copper smelting process, ISASMELT furnace discharges a large amount of matte and slag mixture and the separation of them has an important influence on the recovery of valuable metals. This paper presented a reduction-sulfurization sedimentation process for recovering copper and cobalt from the matte–slag mixture of ISA furnace. Firstly, matte–slag mixture and traditional static sedimentation slag are characterized to determine their mineral composition and occurrence state. It indicates that Cu is primarily lost in slag in the form of sulfide, while Co is mostly lost in the form of oxide. With coke and pyrite as the reducing agent and vulcanizing agent, an orthogonal laboratory experiment was conducted to determine the effects of the smelting temperature and additive dosage on the recovery process. The optimum slag cleaning conditions were found to be: a coke dosage of 2 pct, a pyrite dosage of 2 pct, and a smelting temperature of 1260 °C lasting for 2 hours. In order to improve on the low utilization ratio of additives associated with the industrial sedimentation process, an innovative additive introducing method was put forward which enables the additives to mix and react with slag more adequately. A powder injection device was purpose-made to inject additives into molten slag in dispersion state, and a laboratory experiment was carried out to simulate this process. By injecting 2 pct coke and 2 pct pyrite, the contents of Cu and Co in cleaned slag decreased to 0.46 and 0.01 pct, respectively. It proves that the injection of additives into molten slag is an effective method to recover Cu and Co from the matte–slag mixture of ISA furnace.

36 MATERIALS SCIENCE↗

Distributions of Ag, Bi, and Sb as Minor Elements between Iron-Silicate Slag and Copper in Equilibrium with Tridymite in the Cu-Fe-O-Si System at T = 1250 °C and 1300 °C (1523 K and 1573 K)

New experimental data on the distributions of silver (Ag), bismuth (Bi), and antimony (Sb) between liquid iron-silicate slag and liquid copper metal in equilibrium with tridymite in the Cu-Fe-O-Si system at T = 1250 °C and 1300 °C (1523 K and 1573 K) have been obtained. The experimental methodology involved high-temperature equilibration, rapid quenching of the equilibrated phases, followed by direct measurement of the equilibrium phases with electron probe X-ray microanalysis (EPMA) for measurement of major element concentrations and laser ablation inductively coupled plasma mass spectrometry (LAICPMS) for the measurement of minor element concentrations. The 4-point test approach was employed to confirm the achievement of chemical equilibrium in the current study. Open-system equilibration on quartz substrates in controlled gas atmospheres (CO/CO{sub 2}/Ar) and closed-system equilibration in sealed quartz ampoules were used. The new experimental data resolve significant discrepancies found in previous studies and can be used as input for the development of thermodynamic databases for copper-making processes.

36 MATERIALS SCIENCE↗

Distribution of Ni, Co, Precious, and Platinum Group Metals in Copper Making Process

The distribution coefficients of Ni, Co, Ag, Au, Pt, and Pd between molten copper and silica-saturated iron silicate slags (L{sub Me}{sup Cu/s}) were measured experimentally. The distribution behaviors were studied under typical conditions of copper converting and fire refining, i.e., from 1250 °C to 1350 °C, and from 10{sup −8} to 10{sup −4} atm oxygen partial pressure. The coefficients were determined as the ratios of the trace element weight concentrations measured in situ, directly from the equilibrated metal and slag phases. For the quantitative elemental analysis of the phases, state-of-the-art analytic techniques, including electron probe microanalysis and laser ablation-inductively coupled plasma-mass spectrometry, were employed. The distribution coefficients L{sub Me}{sup Cu/s} determined can be arranged in the following order: Pt > Au > Pd >> Ag > (Cu) > Ni > Co > (Fe).

36 MATERIALS SCIENCE↗

Ultrasound-Assisted Leaching and Kinetic Study of Blended Copper Slag

This article deals with the dissolution of blended copper slag (flash and converter furnace) in hydrogen peroxide and acetic acid in the presence of ultrasound. The parameters that are effective on leaching efficiency, such as leaching temperature, leaching time, ultrasound power, acetic acid concentration, and hydrogen peroxide concentration, were investigated. The optimum leaching conditions for maximum copper dissolution (93 pct) and minimum iron dissolution (3 pct) were determined as follows: 2 M H{sub 2}O{sub 2}, 4 M CH{sub 3}COOH, 10 pct of ultrasound power, 65 °C of leaching temperature, 60 minutes of leaching time, and 1:25 of solid–liquid ratio. According to the Brunauer–Emmett–Teller (BET) analysis results on the original sample and leaching residue, the ultrasound caused formation of microcracks on the particle surface; however, the BET surface area increased and the mean adsorption pore width decreased. The apparent activation energy was found to be 55.35 kJ/mol, and the kinetics equations of the processes were established.

36 MATERIALS SCIENCE↗

Behavior of Ga, In, Sn, and Te in Copper Matte Smelting

The distributions of Ga, In, Sn, and Te between copper-iron mattes and silica-saturated iron silicate slags over a wide range of matte grades 55 to 75 pct Cu were determined at 1300 °C using a gas-phase equilibration-quenching technique and direct phase composition analysis by Electron Probe X-ray Microanalysis and Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry. Alumina from aluminum, a typical minor element of electric and electronic copper scrap, and lime were adopted as slag modifiers for increasing the trace element recoveries. Gallium and tin were distributed predominantly in the slag, indium preferred sulfide matte at low matte grades and slag at high, whereas tellurium strongly favored the sulfide matte in particular in high matte grades. The slag modifiers alumina and lime had a minor impact on the distribution coefficients of gallium and tin, but for indium and tellurium the distribution coefficients were more strongly affected by the basic oxides. The strong tendencies of tin and tellurium to vaporize at the experimental temperature were confirmed.

36 MATERIALS SCIENCE↗

Constitutive Behavior and Processing Map of T2 Pure Copper Deformed from 293 to 1073 K

The deformation behavior of T2 pure copper compressed from 293 to 1073 K with strain rates from 0.01 to 10 s{sup −1} was investigated. The constitutive equations were established by the Arrhenius constitutive model, which can be expressed as a piecewise function of temperature with two sections, in the ranges 293-723 K and 723-1073 K. The processing maps were established according to the dynamic material model for strains of 0.2, 0.4, 0.6, and 0.8, and the optimal processing parameters of T2 copper were determined accordingly. In order to obtain a better understanding of the deformation behavior, the microstructures of the compressed samples were studied by electron back-scattered diffraction. The grains tend to be more refined with decreases in temperature and increases in strain rate.

36 MATERIALS SCIENCE↗

Tensile Properties and Fracture Characteristics of Nanostructured Copper and Cu-SiC Nanocomposite Produced by Mechanical Milling and Spark Plasma Sintering Process

The presence of large grains within nanometric and ultrafine grain matrix is an effective method in order to enhance strength while keeping the high ductility of metals. For this purpose, in this research, spark plasma sintering (SPS) was used to consolidate milled Cu and Cu-SiC powders. In SPS process, local sparks with high temperature between particles take place and locally lead to intense grain growth, and therefore, this method has the ability to produce bimodal grain structures in copper and copper-based composites. Microstructural and mechanical studies showed ≈ 185 and ≈ 437 nm matrix grain sizes, high tensile yield strength values of ≈ 188.4 and ≈ 296.9 MPa, and fracture strain values of 15.1 and 6.7% for sintered Cu and Cu-4 vol.% SiC nanocomposite materials, respectively. The presence of nanoparticles promoted the occurrence of static recrystallization and decreased the fraction of coarse grains in microstructure. The high tensile properties of the produced materials are attributed to fine grain size, homogenous dispersion of nanoparticles and retarded grain boundary migration during sintering.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Microstructure Evolution and Microhardness Distribution of Copper Processed Using Multiple Passes of Elliptical Cross-Sectional Spiral Equal-Channel Extrusion

The aim of this work is to study the effect of six-pass elliptical cross-sectional spiral equal-channel extrusion (ECSEE) on the microstructure and performance of ultrafine-grained (UFG) copper. Equiaxed grains of average grain size of less than 1 μm are formed into shear bands in the low strain region of ECSEE deformed specimen. More homogeneous and equiaxed microstructure with high misorientation angles is obtained in the high strain. Moreover, the microstructure evolution of ECSEE-induced copper is a dynamic equilibrium process of shear deformation accompanying the interactions of high dislocation density, cellular structure and high-angle grain boundaries. The grain ECSEE refinement mechanism is described as the formation process of dislocations, cells, local grain sub-boundaries rotation and large angle grain restructure. The significantly non-uniform hardness distribution is consistent with the deformation behavior and microstructure refinement in the ECSEE-induced specimen. The homogeneity of microstructure and hardness improves as the ECSEE pass increases.

36 MATERIALS SCIENCE↗