Zinc Metal Research Articles

Phytic Acid Customized Hydrogel Polymer Electrolyte and Prussian Blue Analogue Cathode Material for Rechargeable Zinc Metal Hydrogel Batteries.

Zinc anode deterioration in aqueous electrolytes, and Zn dendrite growth is a major concern in the operation of aqueous rechargeable Zn metal batteries (AZMBs). To tackle this,the replacement of aqueous electrolytes with a zinc hydrogel polymer electrolyte (ZHPE) is presented in this study. This method involves structural modifications of the ZHPE by phytic acid through an ultraviolet (UV) light-induced photopolymerization process. The high membrane flexibility, high ionic conductivity (0.085Scm-1), improved zinc corrosion overpotential, and enhanced electrochemical stability value of ≈2.3V versus Zn|Zn2+ show the great potential of ZHPE as an ideal gel electrolyte for rechargeable zinc metal hydrogel batteries (ZMHBs). This is the first time that the dominating effect of chelation of phytic acid with M2+ center over H-bonding with water is described to tune the gel electrolyte properties for battery applications. The ZHPE shows ultra-high stability over 360h with a capacity of 0.50mAhcm-2 with dendrite-free plating/stripping in Zn||Zn symmetric cell. The fabrication of the ZMHB with a high-voltage zinc hexacyanoferrate (ZHF) cathode shows a high-average voltage of ≈1.6V and a comparable capacity output of 63mAhg-1 at 0.10Ag-1 of the current rate validating the potential application of ZHPE.

A congruent-melting rubidium zinc vanadium oxychloride exhibiting strong mid-infrared second-harmonic generation and high laser-induced damage threshold

A novel mid-infrared (MIR) nonlinear optical (NLO) crystal Rb4ZnV5O15Cl (RZVC) has been designed and sythesized by the aliovalent substitution strategy based on the parent structure Rb2(VO)(V2O7). Modification of square pyramidal VO5 units through introduction of chlorine ion and zinc metal caion significantly enhanced the dipole moments in a unit cell from 1.653 D for Rb2(VO)(V2O7) to 6.559 D for RZVC. Consequently, polycrystalline RZVC exhibits strong SHG responses of 12.5 × KDP @1064 nm and 1.2 × AGS @2 μm. Furthermore, RZVC features a congruent melting property, an ultra-high LIDT value (62 × AGS @1064 nm), and a deep IR transparency cutoff edge (10 μm). Most importantly, RZVC can achieve full-wavelength phase matching in a very wide MIR transparency range of 1.69–10 μm, completely covering the important atmospheric window (3–5 μm) through NLO processes. Because of its many outstanding properties, RZVC can be a highly desirable candidate for practical MIR NLO applications.

Exposure to hull cleaning wastewater induces mortality through oxidative stress and cholinergic disturbance in the marine polychaete Perinereis aibuhitensis

While wastewater and paint particles discharged from the in-water cleaning process of ship hulls are consistently released into benthic ecosystems, their hazardous effects on non-target animals remain largely unclear. In this study, we provide evidence on acute harmful effects of hull cleaning wastewater in marine polychaete Perinereis aibuhitensis by analyzing physiological and biochemical parameters such as survival, burrowing activity, and oxidative status. Raw wastewater samples were collected during ship hull cleaning processes in the field. Two wastewater samples for the exposure experiment were prepared in the laboratory: 1) mechanically filtered in the in-water cleaning system (MF) and 2) additionally filtered with a 0.45 μm filter in the laboratory (LF). These wastewater samples contained high concentrations of metals (zinc and copper) and metal–based booster biocides (copper pyrithione and zinc pyrithione) compared to those analyzed in seawater. Polycheates were exposed to different concentrations of the two wastewater samples for 96 h. Higher mortality was observed in response to MF compared to LF–exposed polychaetes. Both wastewater samples dose-dependently decreased burrowing activity and AChE activity. Drastic oxidative stress was observed in response to the two wastewater samples. MDA levels were significantly increased by MF and LF samples. Significant GSH depletion was observed with MF exposure, while increased and decreased GSH contents were observed in LF-exposed polychaetes. Enzymatic activities of antioxidant components, catalase, superoxide dismutase, and glutathione S-transferase were significantly modulated by both wastewater samples. These results indicate that even filtered hull cleaning wastewater can have deleterious effects on the health status of polychaetes.

Achieving Dendrite-Free Zinc Metal Anodes via Molecule Anchoring and lon-Transport pumping.

The potential for scale-up application has been acknowledged by researchers for rechargeable aqueous zinc-ion batteries (ZIBs). Nonetheless, the progress of the development is significantly impeded due to the instability of the interface between the zinc anode and electrolyte. Herein, efficient and environmentally benign valine (Val) were introduced as aqueous electrolyte additive to stabilize the electrode/electrolyte interface (EEI) via functional groups in additive molecules, thus achieving reversible dendrite-free zinc anode. The amino groups present in Val molecules have a strong ability to adsorb on the surface of zinc metal, enabling the construction of anchored molecular layer on the surface of zinc anodes. The strongly polar carboxyl groups in Val molecules can act as ion-transport pumps to capture zinc ions in the electric double layer (EDL) through coordination chemistry. Therefore, this reconstructed EEI could modulate the zinc ion flux and simultaneously suppress side reactions and dendritic growth of Zn. Consequently, a long stable cycling up to 1400 h at a high current density of 20 mA cm-2 is achieved. Additionally, Zn//V2O5 full cell with Val additive exhibit enhanced cyclability, retaining 77 % capacity after 3000 cycles, displaying significant potential in promoting the commercialization of ZIBs.

Mandible elemental composition and mechanical properties from distinct castes of the leafcutter ant Atta laevigata (Attini; Formicidae).

Leafcutter ant colonies are divided into castes with the individuals performing different tasks, based mostly on size. With the mandibles, the small minims care for the brood or the fungus, whereas the larger minors and mediae cut and transport plant material, with the ant size positively related to the material size. The mechanical properties and composition of the mandible cuticle have been previously tested in the soldiers as the largest caste, revealing that the cutting edges contained high contents of the cross-linking transition metal zinc (Zn). With regard to the smaller castes, no data are present. To study how the mandible size and function relates to its mechanical properties, we here tested the mandibles of minims, minors and mediae by nanoindentation. We found that the hardness (H) and Young's modulus (E) values increased with increasing ant size and that the mandible cutting edges in each caste have the highest H- and E-values. To gain insight into the origins of these properties, we characterized the elemental composition by energy-dispersive X-ray analysis, revealing that minors and mediae possessed higher content of Zn in the cutting edges in contrast to the minims containing significantly less Zn. This shows, that Zn content relates to higher mechanical property values. Additionally, it shows that all of these parameters can differ within a single species.

Interfacial Engineering for Oriented Crystal Growth toward Dendrite-Free Zn Anode for Aqueous Zinc Metal Battery.

Zn deposition with a surface-preferred (002) crystal plane has attracted extensive attention due to its inhibited dendrite growth and side reactions. However, the nucleation and growth of the Zn(002) crystal plane are closely related to the interfacial properties. Herein, oriented growth of Zn(002) crystal plane is realized on Ag-modified surface that is directly visualized by in situ atomic force microscopy. A solid solution HCP-Zn (~1.10 at. % solubility of Ag, 30 °C) is formed on the Ag coated Zn foil (Zn@Ag) and possesses the same crystal structure as Zn to reduce its nucleation barrier caused by their lattice mismatch. It merits oriented Zn deposition and corrosion-resistant surface, and presents long cycling stability in symmetric cells and full cells coupled with V2O5 cathode. This work provides insights into interfacial regulation of Zn anodes for high-performance aqueous zinc metal batteries.

Interfacial Engineering for Oriented Crystal Growth toward Dendrite‐Free Zn Anode for Aqueous Zinc Metal Battery

AbstractZn deposition with a surface‐preferred (002) crystal plane has attracted extensive attention due to its inhibited dendrite growth and side reactions. However, the nucleation and growth of the Zn(002) crystal plane are closely related to the interfacial properties. Herein, oriented growth of Zn(002) crystal plane is realized on Ag‐modified surface that is directly visualized by in situ atomic force microscopy. A solid solution HCP‐Zn (~1.10 at. % solubility of Ag, 30 °C) is formed on the Ag coated Zn foil (Zn@Ag) and possesses the same crystal structure as Zn to reduce its nucleation barrier caused by their lattice mismatch. It merits oriented Zn deposition and corrosion‐resistant surface, and presents long cycling stability in symmetric cells and full cells coupled with V2O5 cathode. This work provides insights into interfacial regulation of Zn anodes for high‐performance aqueous zinc metal batteries.

Natural biopolymers derived kinematic and self-healing hydrogel coatings to continuously protect metallic zinc anodes

Zinc (Zn) dendrite growth and hydrogen evolution corrosion reaction of Zn metal anodes greatly affect the cycling performance and hinder the commercial application of high safety aqueous Zn ion batteries. Building an excellent protective layer to perfectly solve the above problems is still a big challenge, resulting from its high-cost raw materials and complicated preparation processes. Herein, in this work, natural pectin biopolymer with galacturonic acid structure was adopted as a functional coating on Zn anodes (Zn@pectin) to realize the excellent cycling properties. Abundant oxygen-containing groups endow pectin films with self-healing ability and response kinematic via multiple intermolecular hydrogen bonds and ligand binding with Zn metal after in-situ gelation with Zn2+ ions, which can sustain the complete structure and fit closely on Zn surface to address the fracture and separation of protective layers with Zn electrode. Functional pectin coatings can serve as a physical barrier to reduce the corrosion effects of H2O molecules in aqueous electrolyte and regular the deposition behavior of Zn2+ ions to hamper the dendrite growth. Zn@pectin symmetric cell can stably cycle for 2500 h at a current density of 2 mA cm−2 and a constant capacity of 2 mAh cm−2. Zn-iodine full batteries possess the high capacity retention of 95 % after 4500 cycles at 1 A g−1. This work provides a new strategy for the protection of Zn metal anodes and realizes the resource utilization of renewable biomass.

Constructing Kosmotropic Salt‐Compatible PVA Hydrogels for Stable Zinc Anodes via Strong Hydrogen Bonds Preshielding Effect

AbstractPhysical hydrogels crosslinked by noncovalent interactions are promising in flexible zinc–metal batteries for their component controllability and environmental friendliness. However, the compatibility of PVA‐based electrolyte and kosmotropic salt remains a challenge, which shows an unclear mechanism. Here, a “good‐to‐poor” solvent substitution strategy is adopted to develop a PVA hydrogel electrolyte with good compatibility with kosmotropic salt (ZnSO4). Stretching the polymer conformation by preshielding the strong intrachain hydrogen bonds with good solvents and activating the polymer interchain interaction in situ with poor solvents will induce the formation of a homogeneous polymer network and the release of hydrated hydroxyl groups for fast ion transport. This multiscale microstructure improves the ionic conductivity and liquid retention of PVA hydrogels with kosmotropic salt. Additionally, this strong hydrogen bonds preshielded hydrogel electrolyte offers great battery performance, with 1300 h of stable cycling at 1 mA cm−2 with low voltage hysteresis; and an extended cycle life of 220 h at 68.4% zinc utilization. Importantly, the Zn//MnO2 pouch cell maintains 98.4% capacity after 100 cycles at 0.2 A g−1 and features strong environmental reliability. These concepts address the inherent barriers of kosmotropic salt‐based hydrogel electrolytes and advance their development in soft electronics.

Extension of Aqueous Zinc Battery Life Using a Robust and Hydrophilic Polymer Separator

AbstractThe use of zinc (Zn) metal as an anode in aqueous batteries offers an eco‐friendly and cost‐effective energy storage solution. However, Zn dendrite formation severely restricts the cycle life of the battery toward practical application. Herein, a commercially hydrophilic polytetrafluoroethylene (PTFE) membrane is demonstrated as a separator to significantly extend the cycle life of the Zn metal anode. In contrast with the conventional fragile glass fiber separator, a wetted PTFE separator exhibited high mechanical strength (stress of 34.3 MPa at 41.4% strain) and favorable hydrophilicity, which both efficiently suppress dendrite growth. The uniform and robust pore structures are proven to facilitate a homogeneous Zn2+ ion flux and a high transfer number of Zn2+ (0.81), which has guaranteed reversible Zn plating/stripping. As a proof of concept, the PTFE separator extended the cycle life considerably to over 3000 h and promoted a Zn plating/stripping efficiency of 99.5% in the unmodified 2 m ZnSO4 aqueous electrolyte. This advancement underscores the significant potential of the PTFE separator for enhancement of the cycling durability of aqueous zinc‐ion batteries (AZIBs).

ТЕРМОДИНАМИЧЕСКИЙ АНАЛИЗ ОКИСЛИТЕЛЬНО – ВОССТАНОВИТЕЛЬНЫХ РЕАКЦИЙ, ПРОТЕКАЮЩИХ ПРИ ГАЛЬВАНОКОАГУЛЯЦИОННОЙ ОЧИСТКЕ СТОКОВ

Abstract. One of the most important environmental problems is the purification of industrial wastewater from heavy metal ions. Various methods are used to solve this problem: chemical, physico-chemical, sorption, but the most promising method for cleaning industrial wastewater containing heavy metal ions, namely copper, nickel and zinc, is the galvanocoagulation method. However, the literature does not sufficiently cover the processes of cementation of heavy metals on cathode loading. A physico-chemical approach to this process is necessary to confirm the process of separation of heavy metal ions from wastewater in the form of sediment and the creation of new industrial wastewater treatment schemes. The composition of the loading is essential in galvanocoagulation neutralization, therefore, in order to determine the effect of the type of active loading, a carbon mineral sorbent (SGN) obtained from ores of cryptocrystalline graphite (Noginsky deposit of the Krasnoyarsk Territory) was used. The studies were carried out in a galvanocoagulation module by passing wastewater through a loading consisting of a mixture of iron shavings and granules of carbon mineral sorbent based on ores of cryptocrystalline graphite (SGN). At the same time, the air dispersed in the lower part of the device was bubbled through the loading. As a result of the operation of the Fe-SGN short-circuited galvanic cell, iron scrap was dissolved and its intensive oxidation to Fe3+ by air oxygen. The article considers the mechanism of galvanocoagulation neutralization of wastewater based on thermodynamic analysis of redox reactions occurring during galvanocoagulation wastewater treatment.
 Subject of the study: both model and real wastewater from the production of electroplating coatings containing copper, zinc and nickel ions with the following concentrations were used: =60 mg/dm3; =15 mg/dm3; =20 mg/dm3
 Materials and methods: galvanocoagulation neutralization using a short-circuited Fe-SGN galvanic cell (carbon mineral sorbent)
 Results: the physico-chemical patterns of the galvanocoagulation process of wastewater treatment have been studied and the thermodynamic parameters of heavy metal ion reduction reactions have been determined
 Conclusions. It has been experimentally established that it is possible to intensify the process of galvanocoagulation of wastewater containing heavy metal ions by using a carbon mineral sorbent as a cathode loading, which reduces the processing time with a high purification effect and a difficult-to-dissolve precipitate is formed.

Effects of multiple metals exposure on abnormal liver function: The mediating role of low-density lipoprotein cholesterol

Equilibration of metal metabolism is critical for normal liver function. Most epidemiological studies have only concentrated on the influence of limited metals. However, the single and synergistic impact of multiple-metal exposures on abnormal liver function (ALF) are still unknown. A cross-sectional study involving 1493 Chinese adults residing in Shenzhen was conducted. Plasma concentrations of 13 metals, including essential metals (calcium, copper, cobalt, iron, magnesium, manganese, molybdenum, zinc, and selenium) and toxic metals (aluminum, cadmium, arsenic, and thallium) were detected by the inductively coupled plasma spectrometry (ICP-MS). ALF was ascertained as any observed abnormality from albumin, alanine transaminase, aspartate transaminase, γ-glutamyl transpeptidase, and direct bilirubin. Diverse statistical methods were used to evaluate the single and mixture effect of metals, as well as the dose-response relationships with ALF risk, respectively. Mediation analysis was conducted to evaluate the role of blood lipids in the relation of metal exposure with ALF. The average age of subjects was 59.7 years, and 56.7 % were females. Logistic regression and the least absolute shrinkage and selection operator (LASSO) penalized regression model consistently suggested that increased levels of arsenic, aluminum, manganese, and cadmium were related to elevated risk of ALF; while magnesium and zinc showed protective effects on ALF (all p-trend < 0.05). The grouped weighted quantile sum (GWQS) regression revealed that the WQS index of essential metals and toxic metals showed significantly negative or positive relationship with ALF, respectively. Aluminum, arsenic, cadmium, and manganese showed linear whilst magnesium and zinc showed non-linear dose-response relationships with ALF risk. Mediation analysis showed that LDL-c mediated 4.41 % and 14.74 % of the relationship of plasma cadmium and manganese with ALF, respectively. In summary, plasma aluminum, arsenic, manganese, cadmium, magnesium, and zinc related with ALF, and LDL-c might underlie the pathogenesis of ALF associated with cadmium and manganese exposure. This study may provide critical public health significances in liver injury prevention and scientific evidence for the establishment of environmental standard.

Trigger a multi-electron reaction by tailoring electronic structure of VO2 toward more efficient aqueous zinc metal batteries

VO2 (B) is recognized as a promising cathode material for aqueous zinc metal batteries (AZMBs) owing to its remarkable specific capacity and its unique, expansive tunnel structure, which facilitates the reversible insertion and extraction of Zn2+. Nonetheless, challenges such as the inherent instability of the VO2 structure, poor ion/electron transport and a limited capacity due to the low redox potential of the V3+/V4+ couple have hindered its wider application. In this study, we present a strategy to replace vanadium ions by doping Al3+ in VO2. This approach activates the multi-electron reaction (V4+/V5+), to increase the specific capacity and improve the structural stability by forming robust V5+O and Al3+O bonds. It also induces a local electric field by altering the local electron arrangement, which significantly accelerates the ion/electron transport process. As a result, Al-doped VO2 exhibits superior specific capacity, improved cycling stability, and accelerated electronic transport kinetics compared to undoped VO2. The beneficial effects of heterogeneous atomic doping observed here may provide valuable insights into the improvement electrode materials in metal-ion battery systems other than those based on Zn.

Constructing Highly Stable Zinc Metal Anodes via Induced Zn(002) Growth.

The nonuniform electric field at the surface of a zinc (Zn) anode, coupled with water-induced parasitic reactions, exacerbates the growth of Zn dendrites, presenting a significant impediment to large-scale energy storage in aqueous Zn-ion batteries. One of the most convenient strategies for mitigating dendrite-related issues involves controlling crystal growth through electrolyte additives. Herein, we present thiamine hydrochloride (THC) as an electrolyte additive capable of effectively stabilizing the preferential deposition of the Zn(002) plane. First-principles calculations reveal that THC tends to adsorb on Zn(100) and Zn(101) planes and is capable of inducing the deposition of Zn ion onto the (002) plane and the preferential growth of the (002) plane, resulting in a flat and compact deposition layer. A THC additive not only effectively suppresses dendrite growth but also prevents the generation of side reactions and hydrogen evolution reaction. Consequently, the Zn||Zn symmetric battery exhibits long-term cycling stability of over 3000 h at 1 mA cm-2/1 mAh cm-2 and 1000 h at 10 mA cm-2/10 mAh cm-2. Furthermore, the NH4V4O10||Zn full battery also displays excellent cycling stability and a high reversible capacity of 210 mAh g-1 after 1000 cycles at 1 A g-1, highlighting a significant potential for practical applications.

A zinc-embedded multicomponent copolymer customized for polypropylene and its synergistic flame-retardant effect and outstanding mechanical properties

The poor compatibility between the common polar intumescent flame-retardant system (IFR) and the nonpolar polypropylene (PP), as well as the high additive amount, seriously impacts the mechanical properties of the composites. This study introduced collaborative flame-retardant technology to construct block copolymer flame retardants and prepared a zinc-embedded multicomponent copolymer (PM-Zn2+) customized for PP composites. In the PM-Zn2+ system, zinc oxide was embedded into the copolymer composed of piperazine phosphate oligomer and melamine phosphate. PM-Zn2+ exhibited an amorphous structure with extremely low crystallinity and demonstrated specific morphological adaptability. The PM-Zn2+ were well dispersed in the PP matrix and changed their morphology during processing. When applied to PP, excellent flame retardancy and mechanical properties were obtained by using a minimal amount of flame retardants (20 %). PM-2 %Zn2+ gave PP an LOI value of 31.5 %, and achieved a UL94 V-0 rating (1.6 mm thick), exhibiting a lower heat release rate and smoke release. The flame-retardant mechanisms of PM-Zn2+ mainly involved the synergistic and aggregative effects. Transition metal zinc synergistically interacted with polyphosphate groups to create a charring barrier effect and enhance synergistic smoke suppression, leading to a significant reduction in combustion intensity. In comparison to the Mix-Zn/PP composites, the mechanical properties of PM-Zn2+/PP were significantly enhanced due to the specific morphological adaptability and improved compatibility. The elongation at break increased significantly from 15.6 % to 627.9 %, marking a remarkable improvement of 40-fold improvement, while the impact strength rose from 23.7 kJ/m2 to 54.3 kJ/m2, representing a 129 % enhancement. Finally, the zinc-embedded multicomponent block copolymer offers a promising approach to developing high-performance flame-retardant polypropylene materials.

Preparation of stable multilayer PDMS composite pervaporation membrane incorporated with in-situ transformed metal organic frameworks for enhanced butanol recovery

In this study, stable and non-defective multilayer polydimethylsiloxane (PDMS) composite pervaporation mixed matrix membranes incorporated with in-situ transformed metal organic frameworks was successfully synthesized via ligand vapor phase infiltration and spin-coating. Metal zinc sources were uniformly distributed in PDMS which were in-situ transformed into homogeneous zeolitic imidazolate framework-8 (ZIF-8) nanoparticles, effectively alleviating the aggregation of ZIF-8. Thermal cross-linking of PDMS and the formation of MOFs occurred simultaneously, omitting the complicated preparation and re-dispersion steps of MOF nanoparticles. MOF nanoparticles and PDMS formed a more stabilized composite structure by in-situ transformation, in which PDMS and metal of MOFs can interact with the -Si-O- of silane coupling groups on membrane surface to construct solid multilayer composite membrane, ensuring long-term stability. Moreover, with the aid of hydrophobic interlayer, polymer infiltration into channels of substrate was restricted and casting solution spread out smoothly, facilitating the formation of defect-free PDMS selective layer. Various techniques including Attenuated Total Reflection-Fourier Transform Infrared Spectrometer, Field Emission Scanning Electron Microscopy, Atomic Force Microscope and X-ray Diffraction were applied to explore the morphology, composition and structure of nanoparticles and membranes, and pervaporation tests were taken to investigate the behavior of hydrophobic polymer-based multilayer membranes. For the recovery of low concentration n-butanol, the prepared non-defective multilayer TAO/ZIF-8/K-PDMS composite membrane displayed excellently total permeate flux of 2890 g m−2 h−1 with competitive separation factor of 40.3.

Recycling potential of secondary zinc materials

Circularity is a decisive corner stone of a sustainable use of raw materials. This has been recognized at global level and is pushed forward specifically in Europe and e.g., Japan. Based on intensive desk top research and interviews with experts from the zinc industry, information on secondary raw materials for zinc recovery was compiled. This paper comprises of an overview of zinc bearing wastes, residues, and by-products occurring in all stages of zinc mining, production, as well as first-use and end-use production. These materials are quantified and characterized, and ways of recycling are described.As a result, potentials for an increase of zinc recycling rates are identified. Mine tailings are a meaningful resource for zinc recovery. Industrial wastes occurring in zinc smelters, such as Jarosite, Goethite, and their likes are in the scope of research projects aiming at recycling zinc and other valuable metals. Residues, ashes, drosses, slags that are produced in first use operation of the zinc value chain, such as galvanizing, zinc die casting, or brass plants are recycled almost completely in Europe and in many other regions in the world. The biggest potential for increasing recycling rates for zinc still lies in steel mill dusts. Also, the majority of zinc die cast parts seem to end up in waste incineration and dump sites. This low end-of-life zinc recycling rate bears room for additional recycling opportunities via an improvement of the intelligent collection and sorting of waste and other innovative recycling processes utilizing residues from waste-to-energy plants.

Development and experimental characterization study of cesium doped zinc oxide polymer conductive films for sensing applications

Development and experimental characterization study of cesium doped zinc oxide polymer conductive films for sensing applications

Technology Selection for Slag Zinc Fuming Process

Circular economy and multi-metal extraction philosophies more and more encourage smelters to reprocess their by-products most significant of which is slag for recovery of valuable metals. Zinc, for instance, can be introduced to lead and copper smelting operations through different sources, including the recycling of waste electric and electronic equipment. During the conventional smelting processes from primary resources, or even those that are particularly developed for recycling purposes, e.g., Black Copper route, the zinc is typically deported to the slag phase as zinc oxide. Recovery of zinc from slag is typically carried out via a slag zinc fuming operation, where a reductant is used to reduce zinc oxide and volatilize zinc metal. In most cases, volatilized zinc is re-oxidized to produce zinc oxide, which can then be sent to hydrometallurgical unit processes for refining. Several technologies and reactors have been developed for efficient and cost-effective fuming processes, none of which can be considered the “best” and most suitable technology for all applications and smelter conditions/slag compositions. This paper reviews the advantages and disadvantages of each of the available technologies and recommends the most suitable process for common conditions.

Toward an Understanding of the Anisotropy in Hcp Zinc Metal: Total Scattering Structural Study Using Synchrotron-Based, Temperature-Dependent, X-Ray Pair Distribution Function Analysis

Abstract: Among hexagonal close packing (hcp) metals, zinc has a non-ideal hcp structure due to a significantly increased axial ratio c/a. We studied the behavior of the ratio of lattice constants c/a and the ratio of thermal displacement parameters (U_33 / U_11) in the temperature range of 100-300 K, using the X-ray total scattering atomic pair distribution function (PDF) analysis over different refinement r-ranges. The temperature-dependent PDF analysis confirmed that the crystal structure of zinc has significant static distortion along the c-direction. The measured value of atomic displacement parameters of zinc showed a notable anisotropy as expressed by the ratio U_33 / U_11 of ≈ 2.2 at 100 K. The lattice parameter ratio c/a was slightly reduced at low temperatures but remained unusually large. The extrapolated value of the ratio c/a reached 1.832 at 0 K. The PDF refinements using the crystallographic model revealed that there are some local structure features in zinc that are not captured by the crystallographic model. On the other hand, our local structure refinement indicated a presence of local bond distortion along the z-direction that averaged out over wider r-range refinements with a large U_33 value. Keywords: Hcp anisotropy, Zinc metal, Total scattering, X-ray scattering, Pair distribution function. PACs numbers: 61.46.Df, 61.10.-i, 78.66.Hf, 61.46.-w.