Residual Copper Research Articles

Electrocatalytic degradation of ofloxacin by self-doped copper/carbon cathode materials derived from waste printed circuit boards

Using residual copper metal from waste circuit boards, ordered carbon materials containing copper (PCBs-Cu-800) were synthesized by self-doping for the electrocatalytic degradation of ofloxacin (OFL). Although PCBs-Cu-800 has a smaller specific surface area, its efficiency in degrading OFL was higher than that of carbon materials without copper (PCBs-800), reaching 95.9 % within 2 h. The PCBs-Cu-800 electrode can generate a large amount of H2O2 in the initial stage of degradation, thereby increasing the amount of hydroxyl radicals (·OH) generated and removing OFL. Density functional theory simulations were used to calculate the adsorption energies of O2 on both materials, demonstrating that the self-doped copper model was more prone to O2 adsorption, and elucidating the excellent electrocatalytic performance of PCBs-Cu. The residual copper metal in the raw material is important in the electrocatalytic processes. This study presents an environmentally friendly catalytic material capable of effectively degrading OFL in solution using waste circuit boards and further expands the application scope of advanced electrochemical oxidation technology in wastewater treatment.

Materials and manufacturing technology for high reliability rigid-flex multilayer PCB for space 3D-electronics packaging

Rigid-flex Multilayer PCB Technology enables the elimination of several connectors and bulky harness for interconnecting functional electronic systems. This minimizes packaging complexity and reduces performance degradation at high frequencies with an added advantage of reduced weight and volume in high-reliability space electronic packages. Here, only thermo-mechanically stable adhesiveless all polyimide flexible laminate cores and no-flow glass-polyimide prepregs are employed. To overcome the manufacturing issues like registration, coverlay protrusion into the rigid portions, and residual copper deposition at the intersections of flexible and rigid portions; a novel manufacturing process technology is proposed here. The technology has been successfully devised after choosing the most appropriate flexible, rigid, and low-flow prepreg materials. Herein, for the realization of rigid-flex multilayer PCB technology with 2-layers of flex and 8-layers of rigid to meet the functional requirements of the board is presented. The critical registration issues associated with the dissimilar rigid and flexible substrates are successfully addressed to achieve best-fit registration and obtain minimum annular rings of 50 μm in all the inner layers for high reliability. Experimental results manifest that incorporating rigid-flex multilayer PCB technology dramatically reduces weight (>30%) and volume (∼40%) to high-reliability space electronics 3D packaging for static and dynamic applications.

Effect of a novel copper chloride gel on endometrial growth and function in healthy volunteers

Research questionDoes the application of a micro-dose of copper chloride gel increase endometrial production of vascular endothelial growth factor (VEGF) without compromising endometrial function or producing embryo toxicity? DesignAn estimate of optimal dose was made based on cell culture studies. Ten healthy participants received an initial uterine application of placebo gel, followed by copper chloride gel (37.5 μM, 75 μM, or 150 μM dose) in a later hormone replacement cycle. Endometrial biopsies (day 5.5 luteal) and pelvic ultrasound were carried out during each cycle to evaluate endometrial function and growth. Uterine fluid was assessed for residual copper levels on the day of biopsy, and copper chloride gel underwent mouse embryos assay assessment for potential embryo toxicity. ResultsThe copper gel significantly increased endometrial VEGF expression (quantitative polymerase chain reaction), and also increasing endometrial thickness by an average of 2.2 mm compared with matched control cycles. The copper gel did not adversely affect endometrial morphology or maturation (histological dating and molecular receptivity testing), and mouse embryos assay studies showed no evidence of embryo toxicity. Furthermore, uterine cavity flush samples mostly lacked copper, with only negligible amounts present in one sample. ConclusionApplying copper chloride gel to the uterine cavity upregulated endometrial VEGF and significantly increased endometrial thickness and volume. No adverse effects on the endometrium or embryos were observed. Copper chloride gels show promise for treating suboptimal endometrial thickness if the results of this study are confirmed by larger randomized controlled trials.

High-temperature oxidation characteristics of 20CrMnTi electroplated with copper

During high-temperature forming and phase change heat treatment, the steel surface is susceptible to oxidation. This can negatively affect the surface quality of steel parts. The production of antioxidant coatings on the surface of steel parts is important for high-temperature precision forming and heat treatment. In this paper, the high-temperature oxidation tests of 20CrMnTi steel, copper, and 20CrMnTi electroplated with copper are conducted. The 20CrMnTi samples showed varying degrees of mass gain above 900 °C; the copper samples showed varying degrees of mass gain above 700 °C; and the process of mass gain for copper-plated 20CrMnTi followed the same trend as for copper during heating and holding. For heated samples of 20CrMnTi plated with copper, the copper coating was oxidized and residual copper was observed in the oxide layer. The distance between the residual copper and the surface of the sample is greater than between the residual copper and the junction of the plating layer and the substrate. Oxygen diffuses through internal defects in the material at a higher rate than copper oxidation. In this study, an oxygen diffusion model and an antioxidant protective layer model at high temperatures were suggested. The protective layer against oxidation recommended in this research is a dense coating consisting of single crystals or fine grains free of porosities and cracks.

Deep purification of copper from zinc sulfate solution using controllable aging FeS nanoparticles through slow-release sulfide precipitation

The purification of impurity ions within zinc hydrometallurgical solutions significantly impacts the subsequent quality of zinc electrodeposition. Traditional methods for copper removal from zinc solutions suffer from issues like limited reactivity, high consumption, and elevated costs. To address these challenges, controllable aging of FeS nanoparticles was designed, employing temperature variations to facilitate comprehensive copper removal from neutral zinc leachates. The aging process imparts a crystalline structure to the FeS nanoparticles, enabling the slow release of sulfide ions. A temperature of 60°C is regarded as the optimal aging temperature, at which the resultant FeS nanoparticles exhibit an optimal sustained-release performance during the aging process. Temperature has been found to be a crucial factor influencing the sustained-release performance of FeS. Once the reaction temperature surpasses 60°C, the utilization efficiency of S ions in the sustained-release agent can reach over 95%, with a maximum of 98.5%. Under optimal conditions featuring a reaction temperature of 60°C, a reaction duration of 30 minutes, and a solution pH maintained at 1, the dosage aged FeS at the S/Cu (II) ratio of 1.2 times, nearly 100% copper removal rate can be achieved. The maximum removal rate for cadmium does not exceed 2.5%, and the residual copper concentration in the zinc leachate is below 0.2 mg/L. The precipitate obtained is high-purity copper sulfide residue, which contains virtually no zinc. Slow-release sulfidation can maximize the utilization efficiency of sulfide ions in the solution, reduce the occurrence of competing reactions, and minimize the intermixing of products. It offers advantages such as high selectivity and deep purification.

Enhanced detection of copper residues on citrus surfaces: An innovative copper fenton-catalysed colorimetric approach using creatinine and molybdenum trioxide

Accurate quantification of residual copper from inorganic copper reagents on the surface of citrus fruits is crucial for preventing diseases caused by excessive heavy metal intake. In this study, we developed a rapid colorimetric strategy for copper detection that is enhanced under near-neutral pH conditions, using molybdenum trioxide (MoO3) and creatinine for copper-Fenton catalysis. The introduction of MoO3 enriches the redox reactions of Cu2+/Cu+ within the complex formed by copper ions and creatinine, leading to enhanced copper-Fenton catalytic activity at near-neutral pH. In the presence of H2O2, this system oxidises colourless 3,3′,5,5′-tetramethylbenzidine (TMB) to blue oxTMB, thereby affording a sensitive colorimetric detection platform for Cu2+. The designed method offers high sensitivity for Cu2+ detection, with a linear range of 0.011.0 μg/mL and a detection limit as low as 0.007 μg/mL. This method was effectively used to analyse copper reagent residues on citrus surfaces, achieving recovery rates of 92.0%115.0%. With its high sensitivity, selectivity, simplicity, and low cost, this colorimetric method shows great potential as an effective approach for determining copper ion levels, particularly for monitoring copper residues in agricultural products.

A stable Copper-Modified silica microsphere catalyst for the synthesis of N-substituted carbazoles and organosilanes

Carbenes are key precursors for various transformations and are applied broadly in the synthesis of complex molecules and drug. Typically, such transformations require expensive metal and complex ligands, leading to a vigorous reaction system and trace metal residues. Herein, we report copper-modified silica microspheres (SM-b) as heterogeneous catalyst in the insertion reaction of diazo compounds with carbazole and silanes. Under this strategy, the optimal SM-b catalyst can prevent the reaction from being too vigorous and can be reused in continuous reactions. Furthermore, gram-scale and catalyst recycling reactions have been proven as the potential industrial applications of the SM-b catalysts. Inductively coupled plasma analysis revealed a residual copper content of only 6.25 ppm in the reaction solution and no detectable copper in the final product, indicating that the residual metal content of the product is far below the FDA-imposed limit of metal impurities.

Preparation of high-purity copper through vacuum distillation

Copper is capable of maintaining strong competitiveness in the metal materials market for its prominent ductility, thermal conductivity, and electrical conductivity. As more rigorous purity requirements of industrial sputtering targets and aerospace have been raised, the clean and efficient production of high-purity copper turns out to be an urgent problem over the past few years. In this paper, the possibility of removing impurities from copper melt was investigated by integrating theoretical calculations and experiments, and the separation coefficient and vapor-liquid equilibrium phase diagram of copper and impurity elements were determined and plotted using the molecular interaction volume model (MIVM). Moreover, the effects of the distillation temperature, the holding time, and the system pressure on the experimental results were discussed. As indicated by the results, with the rise of the temperature and with the extension of the holding time, the purity of copper was first increased and then decreased, and the purity of residual copper reached 99.9993% at 1473 K temperature, 1.5 h holding time, and 5 Pa pressure, and the method effectively separated impurities from copper raw materials. Besides, no waste water or waste gas emission was generated in the experiment.

Study of Factors Affecting the Copper Ore Leaching Process

This paper provides an overview of hydrometallurgical copper extraction studies in which liquid extraction technology has been used with four copper deposits of different compositions. The sulfuric acid consumption rate and copper extraction efficiency, which are dependent on the initial content and forms of calcium compounds and other impurities in ore samples, were calculated, and the results are presented herein. It was established that during the leaching process, silicate compounds of alkaline earth metals, in addition to calcium and magnesium carbonate compounds, would affect the levels of sulfuric acid consumption, thereby actively lowering the acidity of the environment. Moreover, these compounds could partially sorb copper ions from sulfuric acid leaching solutions. Thus, the analysis of waste ore samples showed that residual copper is mainly contained in the form of complex silicate complexes. The presence of divalent iron compounds in the composition from one of the deposits also allowed us to perform a biochemical leaching experiment with preliminary oxidation using an Acidithiobacillus ferrooxidans bacterial culture adapted to the ore composition. The use of this biochemical method in the copper leaching process resulted in a significant reduction in sulfuric acid consumption, by 40%, and a copper recovery rate of 87.2%.

Kinetics and mechanism of oxidizing roasting of sulfide copper-cobalt ore

The aim of the study was to examine the chemistry, kinetics and mechanism of oxidizing roasting of a typical sample of sulfide copper-cobalt ore. The research object was sulfide copper-cobalt ore with the following main minerals: pyrite, pyrrhotite, chalcopyrite, sphalerite, tremolite, silicon dioxide, talc, siderite and calcite. The methodology involved high-temperature X-ray phase analysis (100–900°C), thermogravimetry, differential scanning calorimetry and mass spectrometry of the released gas (30–1100°C, heating rate – 5–20°C·min-1, air flow rate – 30 cm3·min-1). The chemistry, kinetics and mechanism of oxidizing roasting of sulfide copper-cobalt ore with a particle size of <0.1 mm were studied. It was found that the process can be represented as a set of seven elementary reactions: five exothermic reactions (at 398–445, 394–488, 440–498, 433–549 and 451–562°C), corresponding to the intense combustion of iron, copper and zinc sulfides, and two endothermic reactions (at 651–664 and 743–927°C), associated with the decomposition of residual copper and iron sulfates. Kinetic analysis (Kissinger and Augis-Bennett methods, identification of the reaction model by reference function and iterative optimization) of differential scanning calorimetry data in connection with the above reactions showed that the limiting stage of the latter is nucleation and crystal growth. The values of activation energy, pre-exponential factor and Avrami parameter ranged between 140–459 kJ·mol-1, 1.41·104–3.49·1031 with-1 and 1.0–1.7, respectively. It was established that crystallization of the products of elementary reactions is accompanied by an increase in the number of nuclei; new phase nuclei can be formed both on the surface and in the bulk of ore particles. The crystal growth is one-dimensional and is controlled by a chemical reaction at the interphase boundary or by diffusion of reagents. The results obtained can be applied in the practice of oxidizing roasting of sulfide ores and concentrates.

Harnessing of newly tailored poly (acrylonitrile)-starch nanoparticle graft copolymer for copper ion removal via oximation reaction as a calorimetric sensor

Purpose Herein, this study aims to use our recently tailored and fully characterized poly acrylonitrile (AN)-starch nanoparticle graft copolymer having 60.1 graft yield percentage as a starting substrate for copper ions removal from wastewater effluent after chemical modification with hydroxyl amine via oximation reaction as a calorimetric sensor. Design/methodology/approach The calorimetric sensor batch technique was used to determine the resin's adsorption capacity, while atomic adsorption spectrometry was used to determine the residual copper ions concentration in the filtrate before and after adsorption. This was done to convert the copolymer's abundant nitrile groups into amidoxime groups, and the resulting poly (amidoxime) resin was used as a copper ion adsorbent. To validate the existence of amidoxime groups, the resin was qualitatively characterized using a rapid vanadium ion test and instrumentally using Fourier transform infrared spectroscopy spectra and scanning electron microscopy morphological analysis. Findings At pH 7, 400 ppm copper ions concentration and 0.25 g adsorbent at room temperature, the overall adsorption potential of poly (amidoxime) resin was found to be 115.2 mg/g. The process's adsorption, kinetics and isothermal analysis were examined using various variables such as pH, contact time, copper ion concentration and adsorbent dose. To pretend the adsorption kinetics, various kinetics models, including pseudo-first-order and pseudo-second-order, were applied to the experimental results. The kinetic analysis indicated that the pseudo-second-order rate equation promoted the development of the chemisorption phase better than the pseudo-first-order rate equation. In the case of isothermal investigations, a study of observed correlation coefficient (R2) values indicated that the Langmuir model outperformed the Freundlich model in terms of matching experimental data. Originality/value To the best of the author's information, there is no comprehensive study for copper ions removal from waste water effluent using the recently tailored and fully characterized poly (AN)-starch nanoparticle graft copolymer having 60.1 graft yield percentage as a starting substrate after chemical modification with hydroxyl amine via oximation reaction as a calorimetric sensor.

Enhanced corrosion inhibition of copper in acidic environment by cathodic control of interface formation with 2-mercaptobenzothiazole

Electrochemistry along with advanced surface analyzes (X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry) were implemented to investigate copper corrosion inhibition by 2-mercaptobenzothiazole (2-MBT) in hydrochloric aqueous solution and the effects of electrochemical control on the formation of the inhibiting interface. It is shown that reducing the native surface oxide by cathodic reduction prior to exposure to the inhibitor drastically decreases the rate of anodic dissolution. Additionally, increasing the exposure time of the metal surface to the inhibitor results in even better protection against dissolution. 2-MBT adsorbs as multilayers and bonds to both metallic copper and residual copper oxide islands via its sulphur atoms. Partial dissociation of the molecule, releasing the exocyclic sulphur, which then bonds to metallic Cu, is observed. Further dissociation of the molecule, releasing the endocyclic sulphur, is induced by anodic polarization, forming defects in the organic layer and thus compromising the barrier properties of the organic layer.

Vertically Aligned Bismuthene Nanosheets on MXene for High-Performance Capacitive Deionization.

Capacitive deionization has been considered as a promising solution to the challenge of freshwater shortage due to its high efficiency, low environmental footprint, and low energy consumption. However, developing advanced electrode materials to improve capacitive deionization performance remains a challenge. Herein, the hierarchical bismuthene nanosheets (Bi-ene NSs)@MXene heterostructure was successfully prepared by combining the Lewis acidic molten salt etching and the galvanic replacement reaction, which achieves the effective utilization of the molten salt etching byproducts (residual copper). The vertically aligned bismuthene nanosheets array evenly in situ grown on the surface of MXene, which not only facilitate ion and electron transport as well as offer abundant active sites but also provide strong interfacial interaction between bismuthene and MXene. Benefiting from the above advantages, the Bi-ene NSs@MXene heterostructure as a promising capacitive deionization electrode material exhibits high desalination capacity (88.2 mg/g at 1.2 V), fast desalination rate, and good long-term cycling performance. Moreover, the mechanisms involved were elaborated by systematical characterizations and density functional theory calculations. This work provides inspirations for the preparation of MXene-based heterostructures and their application for capacitive deionization.

Synthesis and Catalytic Studies of Thermoresponsive Copper (I) Complex towards Click Reactions

AbstractClick reaction or copper‐assisted azide–alkyne cycloaddition (CuAAC) reaction can conveniently synthesize desired organic molecules or functionalize biological macromolecules. In many cases, trace amounts of residual copper from the reaction mixture are not trivial to remove when the exhaustive purification step is avoided to fulfill the essential criteria of a click reaction. It is often detrimental, particularly for biochemical applications or when it involves biological macromolecules. Herein, we have reported the synthesis of a new type of copper (I) complex as a smart catalyst for click reaction, which can be separated from the reaction mixture very easily by the slight elevation of temperature, thanks to its thermoresponsive behavior. The click reactions using a thermoresponsive catalyst were first studied in an aqueous medium using various organic molecules containing alkyne and azide functional groups. Later, the strategy was extended to biological macromolecules like collagen.

Manufacturing studies and rf test results of the 1.3 GHz fundamental power coupler prototypes

The superconducting radiofrequency electron linear accelerator of the Shanghai HIgh repetition rate XFEL aNd Extreme light facility (SHINE) will use 600 TESLA-style cavities with 1.3 GHz fundamental power couplers for continuous-wave operation. The first batch of 26 1.3 GHz coupler prototypes has been fabricated from three domestic manufacturers for qualification. Several key manufacturing processes have been developed and qualified, including high residual resistivity ratio copper plating, vacuum brazing of ceramic windows, electron beam welding, and titanium nitride coating. In addition, uniform quality control and inspection processes have been established to ensure the power couplers meet the requirements for the intended use in the SHINE project. All the 1.3 GHz coupler prototypes have been power conditioned with 14-kW traveling wave and 7-kW standing wave rf in continuous-wave mode. Even higher power levels have been demonstrated with 20-kW traveling wave and 10-kW standing wave rf, which indicates their robustness.11 MoreReceived 27 July 2022Accepted 7 November 2022DOI:https://doi.org/10.1103/PhysRevAccelBeams.25.113501Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI.Published by the American Physical SocietyPhysics Subject Headings (PhySH)Research AreasSuperconducting RFAccelerators & Beams

Suppressing Undesired Channel Length‐Dependent Electrical Characteristics of Fully Integrated InGaZnO Thin‐Film Transistors via Defect Control Layer

AbstractDemand for increased scalability of oxide thin‐film transistors (TFTs) continues to rise, along with the need for ever‐higher integration densities and driving currents. However, the undesirable channel length (LCH)‐dependency renders short channels difficult. To overcome such behavior in back‐channel etched devices, back‐channel interface engineering using commercially favorable silicon oxide (SiOx) and the effects thereof on the electrical characteristics of fully integrated TFTs are investigated. Process‐dependent investigation reveals that a sequential formation of double‐layered SiOx with a defect control layer (DCL) effectively alleviates back‐channel damage. The proposed method imparts advanced functionality to conventional materials of SiOx. The DCL promotes oxygen inter‐diffusion to the oxygen‐deficient back‐channel, suppresses excess hydrogen inflow, and boosts out‐diffusion of residual copper from the back‐channel. This afforded excellent device uniformity and electrical characteristics with the proposed device, including field effect mobility of ≈14.0 ± 1.0 cm2 V−1 s−1, threshold voltage (Vth) of ≈1.22 ± 0.39 V, and subthreshold gate swing of ≈0.46 ± 0.09 V dec−1 at W/L = 4/7 µm. Furthermore, Vth variation when LCH decreased from 20 to 4 µm is dramatically suppressed from >11.39 V with the pristine device to 0.78 V with the proposed device, because of controlled back‐channel properties providing sufficient effective LCH.

Changes in Cu accumulation and fractionation along soil depth in acid soils of vineyards and abandoned vineyards (now forests)

This study investigated changes in copper accumulation and fractionation based on the depth of soils obtained from active and abandoned vineyards. Soil samples were collected at different depths in three areas with active and abandoned vineyards, and the concentrations of total copper and copper fractions were measured in these soil samples. Results revealed that in active vineyards, total copper accumulation was the highest in the first layer of soil (depth = 0–2 cm), with concentrations (193–892 mg kg−1) considerably higher than those in the deepest soil layer (depth = 40–50 cm; concentration = 63–71 mg kg−1). This accumulation was significantly correlated with the total carbon concentration in the soil. However, the total copper concentration in abandoned vineyards (84–374 mg kg−1) was the highest in the subsurface layers (depth = 10–15 cm) and was not significantly correlated with the total carbon content. Moreover, the percentage of available copper was lower in abandoned vineyards than in active vineyards. In terms of copper fractionation, the main fraction in active vineyard soil was copper bound to organic matter, whereas the main fraction in abandoned vineyard soil was residual copper. Therefore, vineyard abandonment and its transformation into forest changed the distribution and fractionation of copper based on soil depth, thus decreasing the amount of available copper and improving the soil quality, which could enable new ecosystems.

Distribution, Assessment, and Source of Heavy Metals in Sediments of the Qinjiang River, China.

Heavy metals are toxic, persistent, and non-degradable. After sedimentation and adsorption, they accumulate in water sediments. The aim of this study was to assess the extent of heavy metal pollution of Qinjiang River sediments and its effects on the ecological environment and apportioning sources. The mean total concentrations of Mn, Zn, Cr, Cu, and Pb are 3.14, 2.33, 1.39, 5.79, and 1.33 times higher than the background values, respectively. Co, Ni, and Cd concentrations are lower than the background values. Fe, Co, Ni, Cd, Cr, Cu, and Pb are all primarily in the residual state, while Mn and Zn are primarily in the acid-soluble and oxidizable states, respectively. Igeo, RI, SQGs, and RAC together indicate that the pollution status and ecological risk of heavy metals in Qinjiang River sediments are generally moderate; among them, Fe, Co, Ni, Cd, Cr, and Pb are not harmful to the ecological environment of the Qinjiang River. Cu is not readily released because of its higher residual composition, suggesting that Cu is less harmful to the ecological environment. Mn and Zn, as the primary pollution factors of the Qinjiang River, are harmful to the ecological environment. This heavy metal pollution in surface sediments of the Qinjiang River primarily comes from manganese and zinc ore mining. Manganese carbonate and its weathered secondary manganese oxide are frequently associated with a significant amount of residual copper and Cd, as a higher pH is suitable for the deposition and enrichment of these heavy metals. Lead–zinc ore and its weathering products form organic compounds with residual Fe, Co, Cr, and Ni, and their content is related to salinity. The risk assessment results of heavy metals in sediments provide an important theoretical basis for the prevention and control of heavy metal pollution in Qinjiang River.

Fabrication and Mechanical Properties of High-Durability Polypropylene Composites via Reutilization of SiO2 In-Situ-Synthesized Waste Printed Circuit Board Powder.

This paper focuses on the characterization of the physico-chemical properties, surface modification, residual copper content and in situ hybrid inorganic particle modification of polypropylene (PP) composites reinforced by waste printed circuit board powder (WPCBP). A series of WPCBP/SiO2 hybrids (TSW) were prepared by a sol–gel method at different pH values. Characterization results revealed the in situ generation of SiO2 on the surface of WPCBP, and showed that with an increase in pH value, the size of SiO2 particles increased gradually and the copper content decreased in the TSW powder. The mechanical properties, oxidation induction time (OIT) and thermal properties of PP composites were improved by reinforcement with TSW, which might be ascribed to the formation of serrated interfaces. This work not only develops a powerful method to enhance the properties of PP/WPCBP composites, but also provides an environmentally sustainable approach to the high-added-value reutilization of WPCBP.

Adsorption characteristics of Cu2+ species on cerussite surfaces and implications for sulfidization flotation

Metal ions are unavoidable in pulp solution, and they frequently influence the flotation recovery of minerals, such as by activation or depression. In this work, we systematically investigated the adsorption characteristics of Cu2+ species on cerussite surfaces and the concomitant effect on sulfidization flotation by micro-flotation experiments and surface analysis. The flotation results indicated that the flotation recovery of cerussite was almost unchanged at low Cu2+ concentration in the presence of Na2S, but it decreased at high Cu2+ concentration. X-ray photoelectron spectroscopy indicated that CuCO3 species formed on cerussite surface in the presence of Cu2+, and Pb–S species and Cu–S species formed after Cu2+–Na2S treatment. Time-of-flight-secondary-ion mass spectrometry indicated that the distribution of lead species narrowed and that of copper species broadened with increasing Cu2+ concentration, which demonstrated that Cu2+ covered the mineral surfaces and inherent Pb2+ was shield. Ultraviolet–visible spectroscopy indicated that the stability of cerussite surface increased with increasing amount of added Na2S. Compared with only Na2S treatment, consumption of xanthate was almost unchanged at low Cu2+ concentration, whereas consumption of xanthate considerably increased at high Cu2+ concentration, which may be because xanthate was consumed by the residual copper ions in the pulp solution. Zeta potential measurements indicated that Cu2+ can chemisorb on cerussite surfaces and increasing the Cu2+ concentration facilitates adsorption of copper species, but it inhibits adsorption of Na2S and BX. Therefore, sulfidization flotation of cerussite is not substantially affected by low concentrations of Cu2+, but is greatly affected by high concentrations of Cu2+.