Zinc Salts Research Articles

Anion Chemistry towards On-Site Construction of Solid-Electrolyte Interface for Highly Stable Metallic Zn Anode.

Reversibility of metallic Zn anode serves as the corner stone for the development of aqueous Zn metal battery, which motivates scrutinizing the electrolyte-Zn interface. As the representative organic zinc salt, zinc trifluorosulfonate (Zn(OTf)2) facilitates a broad class of aqueous electrolytes, however, the stability issue of Zn anode remains crucial. The great challenge lies in the lack of Zn anode protection by the pristinely formed surface structure in aqueous Zn(OTf)2 electrolytes. Accordingly, an electrochemical route was developed to grow a uniform zinc trifluorosulfonate hydroxide (ZTH) layer on Zn anode as an artificial SEI, via regulation on metal dissolution and strong coordination ability of zinc ions. Co-precipitation was proposed to be the formation mechanism for the artificial SEI, where the reduction stability of OTf‾ anion and the low-symmetry layer structure of ZTH was unmasked. This artificial SEI favors interfacial kinetics, depresses side reactions, and well maintains its integrity during cycling, leading to a prolonged lifespan of Zn stripping/plating with a high DOD of ~85%, and an improved cycling stability of ~92% retention rate for V2O5/Zn cell at 1 A g-1. The unveiled role of anion on Zn anode drives the contemplation on the surface chemistry for the blooming aqueous rechargeable battery.

A Trio of Revelations: Weakly Solvating Modulation in Aqueous Electrolytes for Zinc Metal Batteries

The emerging concept of weakly solvating electrolytes in multivalent ion aqueous batteries has garnered attention due to their enhanced kinetic performance at a low cost. This article aims to dissect the concept of "weakly solvating electrolyte" into three revelations, i.e., ion solvation, hydrogen bonding strength, and ionic interactions. It is revealed that a weakly interacting solvent must satisfy the requirements of having a solvation strength weaker than ionic interaction than water molecules, as well as disrupting rather than strengthening hydrogen bonding within them. Moreover, electrolyte chemistry requires balancing multiple factors, and the same weakly interacting solvent exhibits varying effects with the variation of the anions of zinc salts. This study offers quantitative descriptors to the concept of weak solvation, particularly for aqueous electrolytes, and provides insights for future electrolyte advancements for multivalent ion batteries.

Synthesis Characterization and Anticancer Activity Studies of the Novel Pyridinyl Zn II and Ni II Metal Complexes

Four novel organometallic complexes were obtained via direct reactions of 2 amino 3 formaldehyde pyridine and 3 4 diaminopyridine with transition metal zinc salts

Zinc for GNAO1 encephalopathy: Preclinical profiling and a clinical case

De novo pathogenic variants in GNAO1-the gene encoding the major neuronal G protein Gαo-cause pediatric encephalopathies and other neurological deficiencies largely refractory to available therapies. Zn2+ emerged to restore guanosine triphosphate hydrolysis and cellular interactions of pathogenic Gαo; dietary zinc salt supplementation improves lifespan and motoric function in a Drosophila disease model. Using biochemical, animal, and first-in-human studies, we provide support for the patient stratification and application of zinc acetate in GNAO1-associated disorders. We show that 16 different pathogenic missense variants cluster in three distinct groups in their responsiveness to Zn2+, and we provide the safety study in a mouse disease model. We further describe treatment of a 3-year-old patient with the common pathogenic GNAO1 variant c607G>A, p.Gly203Arg with oral 50mg zinc (in the form of zinc acetate) daily, as applied in Wilson's disease. During 11months of treatment, the patient shows cessation of daily dyskinetic crises, improved Burke-Fahn Marsden Dystonia Rating Scale movement score, reduction in epileptic seizures, and an excellent safety profile. Our findings warrant a large-scale clinical trial and might set the new standard of care for GNAO1-related disorders. This work was funded by the Russian Science Foundation (grant #21-15-00138) and GNAO1 España.

Improvements and Challenges of Hydrogel Polymer Electrolytes for Advanced Zinc Anodes in Aqueous Zinc-Ion Batteries.

Aqueous zinc-ion batteries (AZIBs) are widely regarded as desirable energy storage devices due to their inherent safety and low cost. Hydrogel polymer electrolytes (HPEs) are cross-linked polymers filled with water and zinc salts. They are not only widely used in flexible batteries but also represent an ideal electrolyte candidate for addressing the issues associated with the Zn anode, including dendrite formation and side reactions. In HPEs, an abundance of hydrophilic groups can form strong hydrogen bonds with water molecules, reducing water activity and inhibiting water decomposition. At the same time, special Zn2+ transport channels can be constructed in HPEs to homogenize the Zn2+ flux and promote uniform Zn deposition. However, HPEs still face issues in practical applications, including poor ionic conductivity, low mechanical strength, poor interface stability, and narrow electrochemical stability windows. This Review discusses the issues associated with HPEs for advanced AZIBs, and the recent progresses are summarized. Finally, the Review outlines the opportunities and challenges for achieving high performance HPEs, facilitating the utilization of HPEs in AZIBs.

Access to 1,3- and 1,5-Disubstituted 1,2,4-Triazoles by Condensation of Acyl Hydrazides with Formamidinium Acetate

AbstractA simple redox-neutral method for the regioselective preparation of 1,3- and 1,5-disubstituted 1,2,4-triazoles from the corresponding unactivated acyl hydrazides and the inexpensive, non-toxic, and shelf-stable formamidinium acetate was developed. The addition of zinc salts proved to be pivotal to ensure full regioselectivity for the 1,3-disubstitution pattern, while 1,5-disubstituted 1,2,4-triazoles could be accessed without. A variety of sensitive functional groups were tolerated, and [1,2,4]triazolo[4,3-a]pyridines were obtained from the corresponding 2-hydrazopyridines without Dimroth rearrangement.

Chitin and Cellulose as Constituents of Efficient, Sustainable, and Flexible Zinc-Ion Hybrid Supercapacitors

A zinc-ion hybrid supercapacitor (ZIHS) is a prospective energy storage device featuring cost-effectiveness, operational safety, environmental friendliness, high-power performance, and satisfied energy density.1 The sustainability of this ZIHS technology is even improved by introducing biopolymer constituents into the cell construction.2 Herein, efficient, sustainable, and flexible ZIHSs employing polysaccharide (chitin- or cellulose-based) components are developed.3 Using green ionic liquid solvents, biopolymer-bound, activated carbon-based cathode materials and hydrogel biopolymer electrolytes containing conductive zinc salts are obtained. According to systematical characterization results, the prepared materials possess favorable functional properties. Biopolymer binders provide homogeneity and integrity within the electrode network and high adhesion to the surface of the current collector. Depending on the type of zinc salt, hydrogel biopolymer electrolytes display high ionic conductivity (up to 46 mS cm−1), expanded electrochemical stability window (up to ca. 2.8 V), and zinc dendrites growth suppression. Biopolymer components assembled with zinc foil electrodes operate efficiently in both coin and pouch ZIHS cell configurations, providing satisfactory energy (45–50 Wh kg−1) and high power (10–20 kW kg−1) density combined with excellent cycle stability. Moreover, these ZIHS pouch-type devices exhibit superior durability and flexibility, withstanding mechanical stress up to 150° bending states with at least 90% of capacitance retention. It suggests a prospect for their application in wearable electronics.4 References(1) Wang, Y.; Sun, S.; Wu, X.; Liang, H.; Zhang, W. Status and Opportunities of Zinc Ion Hybrid Capacitors: Focus on Carbon Materials, Current Collectors, and Separators. Nano-Micro Lett. 2023, 15 (1), 78.(2) Kasprzak, D.; Mayorga-Martinez, C. C.; Pumera, M. Sustainable and Flexible Energy Storage Devices : A Review. Energy & Fuels 2023, 37, 74–97.(3) Kasprzak, D.; Liu, J. Chitin and Cellulose as Constituents of Efficient, Sustainable, and Flexible Zinc-Ion Hybrid Supercapacitors. Sustain. Mater. Technol. 2023, 38, e00726.(4) Dubal, D. P.; Chodankar, N. R.; Kim, D. H.; Gomez-Romero, P. Towards Flexible Solid-State Supercapacitors for Smart and Wearable Electronics. Chem. Soc. Rev. 2018, 47 (6), 2065–2129. Figure 1. Graphical abstract of the research on biopolymer-based Zn-ion hybrid supercapacitors. Figure 1

Electrochemical Characterization of Non-Aqueous and Aqueous Gel Polymer Electrolytes for Zinc-Ion Fiber Batteries

The increasing miniaturization of integrated circuits has enabled a wide variety of new applications for embedded sensors and smart devices. Miniaturization of their power sources, however, has lagged in comparison. There are many challenges to devising a space-conscious battery, including the power density, mechanical stability, and chemical safety. Batteries made in fiber formats are of interest for use in wearable electronics. Recent studies have shown the feasibility of Li-ion battery chemistries in drawn polymer fibers via thermally induced phase separation (TIPS)1,2 but key performance gaps in safety and reliability of these fiber batteries remain.In addition to Li-ion, zinc-manganese dioxide (Zn-MnO2) chemistries are particularly good candidates for fiber format batteries due to their relatively low raw material cost, low reactivity, and tolerance of environmental contaminants such as water. Our work has focused on two Zn-MnO2 gel polymer electrolyte (GPE) cell formats: one non-aqueous polyvinylidene fluoride (PVDF) based gel polymer electrolyte, the other an aqueous polyvinyl alcohol (PVA) based GPE. In this work, we synthesize, characterize, and compare these two electrolyte formats head-to-head in both Zn-Zn symmetric cells and Zn-MnO2 full cells.After the GPEs were synthesized, thermo-gravimetric analysis was used to characterize the gels and evaluate the feasibility of drawing the GPE of interest into fibers. We synthesized zinc salt containing PVDF-based GPEs and characterized them in ionic blocking cells via electrochemical impedance spectroscopy (EIS), achieving conductivities of 1.8 mS/cm2. We also assembled Zn-Zn symmetric cells, investigated key performance characteristics such as the transport number and the electrochemical stability window, and stably cycled them for over 500 hours at 0.5 mA/cm2. Lastly, we assembled Zn-MnO2 full cells to confirm the battery performance.

Zinc Acetate in Organic Synthesis and Catalysis: A Review

Abstract: Among the many zinc salts that can be found, zinc acetate is one of the readily available, affordable, low-hazardous Lewis acids. It can be referred to as a multifunctional catalyst due to its unique physical and chemical properties, which show that they are effective in enabling a variety of synthetic transformations in both organic synthesis and catalysis. This review included noteworthy innovations that have been created during the past two and half decades using zinc acetate as a catalyst or reagent.

Insights Into the Role of Copper in Neurodegenerative Diseases and the Therapeutic Potential of Natural Compounds.

Neurodegenerative diseases encompass a collection of neurological disorders originating from the progressive degeneration of neurons, resulting in the dysfunction of neurons. Unfortunately, effective therapeutic interventions for these diseases are presently lacking. Copper (Cu), a crucial trace element within the human body, assumes a pivotal role in various biological metabolic processes, including energy metabolism, antioxidant defense, and neurotransmission. These processes are vital for the sustenance, growth, and development of organisms. Mounting evidence suggests that disrupted copper homeostasis contributes to numerous age-related neurodegenerative diseases, such as Alzheimer's disease (AD), Parkinson's disease (PD), Huntington's disease (HD), amyotrophic lateral sclerosis (ALS), Wilson's disease (WD), Menkes disease (MD), prion diseases, and multiple sclerosis (MS). This comprehensive review investigates the connection between the imbalance of copper homeostasis and neurodegenerative diseases, summarizing pertinent drugs and therapies that ameliorate neuropathological changes, motor deficits, and cognitive impairments in these conditions through the modulation of copper metabolism. These interventions include Metal-Protein Attenuating Compounds (MPACs), copper chelators, copper supplements, and zinc salts. Moreover, this review highlights the potential of active compounds derived from natural plant medicines to enhance neurodegenerative disease outcomes by regulating copper homeostasis. Among these compounds, polyphenols are particularly abundant. Consequently, this review holds significant implications for the future development of innovative drugs targeting the treatment of neurodegenerative diseases.

Tough Self-Healing Materials via In Situ Growth of Zeolitic Imidazolate Framework-8 Nanocrystals in Polymers.

Construction of self-healing materials with improved mechanical performanceis a great challenge. A strong and tough self-healing composite is fabricated via in situ growth of zeolitic imidazole framework-8 (ZIF-8) nanocrystals in imidazole-containing polymer networks. By adjusting the stoichiometric ratio of the zinc salt to 2-methylimidazole, composites with various mechanical performances are obtained. The existence of ZIF-8 nanocrystals via in situ growth in the polymer networks is confirmed by X-ray diffraction (XRD), transmission electron microscopy (TEM), and atomic force microscopy (AFM). The zinc-imidazole interactions between the ZIF-8 nanocrystals and the polymer are confirmed by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy. The composites can repair themselves under mild conditions owing to dynamic zinc-imidazole interactions. The self-healing efficiency of composites can reach up to 91% under the condition of 60°C for 48h. In contrast to the pure zinc cation crosslinking system, the composite containing ZIF-8 nanocrystals prepared via in situ growth exhibited enhanced tensile strength and toughness by 43% and 100%, respectively. This study proves that incorporating the metal-organic frameworks(MOFs) materials into a self-healing system via an in situ growth strategy is highly promising for designing self-healing materials with improved mechanical performance.

Influence of enzyme drug and adsorbent on digestive metabolism processes of steers fattening in technogenic zone

In the practice of feeding of young ruminants for fattening, feed drugs of new generation adsorbents are increasingly and widely introduced. They often exhibit synergistic eff ects on metabolic processes with a large set of biologically active additives including enzyme drugs. The purpose of the research was to study the infl uence of the adsorbent drugs toxfi n and MEC celloviridin G20x on the state of rumen metabolism in fattening steers in whose diets there was an excess content of lead, zinc and cadmium salts. It was found that in order to activate the processes of digestive metabolism due to better elimination of heavy metal salts, it is advisable to jointly introduce the adsorbent toxfi n in the amount of 1 kg/t of compound feed and MEC celloviridin G20x in the amount of 70 g/t of compound feed into the composition of the rations of fattening steers. The results of the conducted studies showed that by the end of fattening at the age of 18 months the animals of the 4th experimental group had the highest body weight, which surpassed the steers of the 1st control group by 29.20 kg (p < 0.05) or 6.86 %. Relative to the control analogues the steers of the 4th experimental group showed an activation of growth in the forestomachs of ciliates (producers of cellulases and amylases) by 54.26 % (p < 0.05) and bacteria of the Flavobacterium vitarumen group (producers of proteinases) by 29.36 % (p < 0.05). Due to the combined feeding of the adsorbent drugs toxfi n and MEC celloviridin G20x, the processes of detoxifi cation of heavy metal salts were more effective. Therefore, the fattening steers of the 4th experimental group more actively accumulated volatile fatty acids in the rumen fl uid, significantly (p < 0.05) outperforming the animals of the 1st control group in this indicator by 1.68 mmol/100 ml or by 20.71 %.

Zinc Protects against Swine Barn Dust-Induced Cilia Slowing.

Agricultural workers exposed to organic dust from swine concentrated animal feeding operations (CAFOs) have increased chances of contracting chronic lung disease. Mucociliary clearance represents a first line of defense against inhaled dusts, but organic dust extracts (ODEs) from swine barns cause cilia slowing, leading to decreased bacterial clearance and increased lung inflammation. Because nutritional zinc deficiency is associated with chronic lung disease, we examined the role of zinc supplementation in ODE-mediated cilia slowing. Ciliated mouse tracheal epithelial cells were pretreated with 0-10 µg/mL ZinProTM for 1 h, followed by treatment with 5% ODE for 24 h. Cilia beat frequency (CBF) and protein kinase C epsilon (PKCε) activity were assayed. ODE treatment resulted in cilia slowing after 24 h, which was reversed with 0.5 and 1.0 µg/mL ZinPro pre-treatment. No zinc protection was observed at 50 ng/mL, and ciliated cells detached at high concentrations (100 µg/mL). ZinPro alone produced no changes in the baseline CBF and showed no toxicity to the cells at concentrations of up to 10 µg/mL. Pre-treatment with ZinPro inhibited ODE-stimulated PKCε activation in a dose-dependent manner. Based on ZinPro's superior cell permeability compared to zinc salts, it may be therapeutically more effective at reversing ODE-mediated cilia slowing through a PKCε pathway. These data demonstrate that zinc supplementation may support the mucociliary transport apparatus in the protection of CAFO workers against dust-mediated chronic lung disease.

Unveiling the Failure Mechanism of Zn Anodes in Zinc Trifluorosulfonate Electrolyte: The Role of Micelle-like Structures.

Zinc trifluorosulfonate [Zn(OTf)2] is considered as the most suitable zinc salt for aqueous Zn-ion batteries (AZIBs) but cannot support the long-term cycling of the Zn anode. Here, we reveal the micelle-like structure of the Zn(OTf)2 electrolyte and reunderstand the failing mechanism of the Zn anode. Since the solvated Zn2+ possesses a positive charge, it can spontaneously attract OTf- with the hydrophilic group of -SO3 and the hydrophobic group of -CF3 via electrostatic interaction and form a "micelle-like" structure, which is responsible for the poor desolvation kinetics and dendrite growth. To address these issues, an antimicelle-like structure is designed by using ethylene glycol monomethyl ether (EGME) as a cosolvent for highly reversible AZIBs. The modified electrolyte shows lower dissociation ability to Zn(OTf)2 and higher coordination tendency with Zn2+ compared to the Zn(OTf)2 electrolyte, resulting in the unique solvation structure of Zn2+(H2O)1.2(OTf-)2(EGME)2.8, which significantly reduces the charge of micelle, damages the micelle-like structure, and boosts the desolvation kinetics. Moreover, the reduction of EGME and OTf- can form a robust dual-layered SEI with high Zn2+ ion conductivity. Consequently, the Zn/Cu asymmetric coin cell using ZT-EGME can work at a high rate and a capacity of 50 mA cm-2 and 5 mA h cm-2 for more than 120 cycles, while its counterparts using ZT can barely work. Moreover, a 505.1 mA h pouch cell with practical parameters including a lean electrolyte supply of 15 mL A h-1 and an N/P ratio of ∼3.5 can work for 50 cycles.

Unlocking the performance degradation of vanadium-based cathodes in aqueous zinc-ion batteries

Vanadium-based materials stand out as promising cathode options for rechargeable aqueous zinc-ion batteries (ZIBs), primarily because of their high capacity and superior rate capability. Nevertheless, the utilization of vanadium-based cathodes in advancing ZIBs toward commercial viability is hindered by their insufficient stability and a notable lack of comprehension of the mechanisms driving capacity degradation. Herein, we identified the formation of Zn3(OH)2V2O7·2H2O (ZOV) as a key contributor to the capacity decay of vanadium-based cathodes. Through a series of compelling experiments, we revealed that dissolved vanadium ions react with zinc salts or layered zinc hydroxide (formed from H+ insertion) during the immersion or cycling of vanadium-based cathodes in aqueous electrolytes, ultimately leading to the formation of detrimental ZOV. Strong evidence shows that ZOV is inactive for Zn2+ storage owing to the presence of the pure tetrahedral frameworks of vanadium. To suppress the formation of ZOV, adjustments were made to the electrolyte composition, including the solvents and solutes. Consequently, the absence of ZOV enables an impressive capacity retention of 85 % in the ZnSO4 electrolyte after 150 cycles at 0.2 A g−1. Overall, this study directly unlocks the capacity decay mechanism in vanadium-based cathodes and offers valuable insights for the design of innovative electrolytes and novel vanadium-based cathode materials for ZIBs.

Density of lymphocytes in cortex and medulla substance of thymus particles of white rats in normal conditions and under influence of heavy metal salts during three months

The consumption of clean water is the most relevant today, but natural water is delivered to our homes through plastic, iron and galvanized pipes. Metal ions, which are part of the pipe material, can get into drinking water and affect the human body, in particular the thymus. That is why the aim of the work was to determine the density of large, medium and small lymphocytes in the cortex and medulla of the thymus lobules of outbred white male rats of reproductive age when consuming small doses of heavy metal salts with water for three months. The study was conducted on 40 outbred white male rats of reproductive age, which were divided into 4 groups: 1 group – control animals that consumed distilled water; 2 group of animals that consumed aqueous solutions – CuSO4·5H2O at a dose of 0.247 mg/dm3; 3 group – aqueous solution of ZnSO4·7H2O at a dose of 1.505 mg/dm3; group 4 – aqueous solution of FeSO4·7H2O at a dose of 0.5 mg/dm3. Histological, electron microscopic and morphometric research methods were used to study the density of large, medium and small lymphocytes in different zones of the thymus lobules. It was found that in the control group of rats, the density of large lymphocytes is the highest in the subcapsular zone, and the lowest in the medulla. The density of medium lymphocytes is the lowest in the subcapsular zone. The density of small lymphocytes is the lowest in the medulla, and the highest in the cortico-medullary zone. When using CuSO4·5H2O salts with drinking water for three months, there were no significant changes in the density of lymphocytes compared to the control group, except for a slight decrease in the density of large lymphocytes in the cortex of the thymus lobules. The density of lymphocytes in the third group of animals that consumed zinc salts (ZnSO4·7H2O) with drinking water changes significantly: the density of large lymphocytes in the subcapsular zone decreases by 2.3 times, in the cortico-medullary zone it increases by 4.7 times, and in the medulla it increases by 2.7 times; the density of medium lymphocytes decreases in the subcapsular zone by 2 times; the density of small lymphocytes decreases by 1.5 times in the subcapsular zone, in the cortex and cortico-medullary zone – decreases by 1.2 times, and in the medulla by 1.1 times. When using FeSO4·7H2O salts with drinking water for three months, no special changes in the density of lymphocytes were noted: a decrease in the density of large lymphocytes in the subcapsular zone by 1.5 times and by 1.3 times in the cortex was observed; the density of medium lymphocytes decreases by 1.2 times in the cortex, and the density of small lymphocytes decreases by 1.2 times in the subcapsular zone and cortex, and increases by 1.2 times in the medulla, compared to the control group of animals. Ultrastructural changes in the structure of lymphocytes and reticuloepithelial cells were not detected when heavy metal salts were consumed with water. Thus, the study showed that the most toxic for the body are zinc salts (ZnSO4·7H2O), the consumption of which with drinking water in small doses for three months led to significant changes in the density of lymphocytes, compared to the control group experimental animals.

Explorations on the antiviral potential of zinc and magnesium salts against chikungunya virus: implications for therapeutics.

Chikungunya virus (CHIKV), which causes chikungunya fever, is an arbovirus of public health concern with no approved antiviral therapies. A significant proportion of patients develop chronic arthritis after an infection. Zinc and magnesium salts help the immune system respond effectively against viral infections. This study explored the antiviral potential of zinc sulphate, zinc acetate, and magnesium sulphate against CHIKV infection. The highest non-toxic concentration of the salts (100 µM) was used to assess the prophylactic, virucidal, and therapeutic anti-CHIKV activities. Dose-dependent antiviral effects were investigated to find out the 50% inhibitory concentration of the salts. Entry bypass assay was conducted to find out whether the salts affect virus entry or post entry stages. Virus output in all these experiments was estimated using a focus-forming unit assay, real-time RT-PCR, and immunofluorescence assay. Different time- and temperature-dependent assays revealed the therapeutic antiviral activity of zinc and magnesium salts against CHIKV. A minimum exposure of 4 hours and treatment initiation within 1 to 2 hours of infection are required for inhibition of CHIKV. Entry assays revealed that zinc salt affected virus-entry. Entry bypass assays suggested that both salts affected post-entry stages of CHIKV. In infected C57BL6 mice orally fed with zinc and magnesium salts, a reduction in viral RNA copy number was observed. The study results suggest zinc salts exert anti-CHIKV activity at entry and post entry stages of the virus life cycle, while magnesium salt affect CHIKV at post entry stages. Overall, the study highlights the significant antiviral potential of zinc sulphate, zinc acetate, and magnesium sulphate against CHIKV, which can be exploited in designing potential therapeutic strategies for early treatment of chikungunya patients, thereby reducing the virus-associated persistent arthritis.

From waste to added-value product: A case of efficient separation and recovery of zinc and iron from spent galvanizing acid

Spent galvanizing acid solution contains high concentrations of zinc salts, ferrous salts, and residual acids, exhibiting extremely high value-added recovery potential. However, achieving the efficient extraction and separation of Zn over Fe becomes particularly challenging under elevated Zn ion concentration. Here, the key extraction parameters, such as modifier ratio, Cyanex 923 concentration and ratio of organic phase to aqueous phase (O/A), are investigated. The stripping and regeneration of extractant, extraction mechanism, as well as high-value recovery of Zn and Fe resources are also comprehensively expounded. After the two-stage extraction, the extraction efficiency of Zn and Fe is 98.92 ​% and 2.09 ​%, respectively. Moreover, the stripping efficiency of Zn reaches 92.3 ​% with O/A ratio of 1 : 2, using oxalic acid as stripping agent. The predominant extracted species is confirmed to be ZnCl3−, resulting in the formation of HZnCl3∙R3PO complex. More importantly, the regenerated extractant can be recycled back into the extraction process, and the reproduced HCl, high-value recovered ZnO and Fe2O3 can be used for different industrial fields. These findings lay a solid foundation for the efficient separation and comprehensive recovery of high-concentration spent galvanizing acid solution.

Characteristics of patients with Wilson disease in the United States: An insurance claims database study.

Wilson disease (WD) is a progressive, potentially fatal degenerative disease affecting the liver and central nervous system. Given its low prevalence, collecting data on large cohorts of patients with WD is challenging. Comprehensive insurance claims databases provide powerful tools to collect retrospective data on large numbers of patients with rare diseases. To describe patients with WD in the United States, their treatment and clinical outcome, using a large insurance claims database. This retrospective, longitudinal study was performed in the Clarivate Real-World Data Product database. All patients with ≥ 2 claims associated with an International Classification of Diseases 10 (ICD-10) diagnostic code for WD (E83.01) between 2016 and 2021 were included and followed until death or study end. Patients were divided into two groups by whether or not they were documented to have received a specific treatment for WD. Clinical manifestations, hospitalisations, liver transplantation and death were documented. Overall, 5376 patients with an ICD-10 diagnostic code for WD were identified. The mean age at inclusion was 41.2 years and 52.0% were men. A specific WD treatment was documented for 885 patients (15.1%), although the number of patients taking zinc salts may be underestimated due to over the counter purchase. At inclusion, the mean age of patients with a documented treatment was 36.6 ± 17.8 years vs 42.2 ± 19.6 years in those without a documented treatment. During follow-up, 273 patients (5.1%) died. Compared with the American general population, the standardised mortality ratio was 2.19. The proportion of patients with a documented WD-specific treatment who died during follow-up was 4.0% and the mean age at death 52.7 years. Patients treated for WD in the United States had an excess early mortality compared with the American population. These findings indicate that there is a significant unmet need for effective treatment for WD in the United States.

Hydrated eutectic electrolyte promotes the preferential growth of Zn (0 0 2) plane and suppresses side reaction for high-stability zinc anodes

Using deep eutectic solvent (DES) electrolytes is an efficient way to suppress the Zn dendrite growth and the side reactions resulting from the high activity of H2O in aqueous zinc-ion batteries (ZIBs). However, most DESs consist of expensive/explosive zinc salts or flammable/toxic organic ligands, which hinders their practical application in ZIBs. Herein, a low-cost and high-safety hydrated eutectic electrolyte based on ZnCl2, urea, and a small amount of H2O is prepared. Due to the low content of H2O and the strong intermolecular interaction between urea and H2O, the activity of H2O is greatly restricted and therefore H2O-induced side reactions are improved. In addition, X-ray photoelectron spectroscopy spectra and density functional theory calculations reveal that the adsorption of urea molecules on the zinc surface forms an organic protective layer, which can induce the preferential growth of the Zn (0 0 2) plane. As a result, with the optimal electrolyte, the Zn||Zn symmetric cell shows a long cyclic life of 1200 h, and the Zn||Cu half-cell delivers a high average Coulombic efficiency of 99.7 % for 2500 cycles. Meanwhile, the Zn||Bi2Te3 and Zn||polyaniline full cells with DES exhibit improved cycling performances compared to those using traditional ZnSO4 electrolyte. This work offers a new perspective to explore low-cost, non-toxic, and high-security DESs for ZIBs.