Amount Of Mn Research Articles

Mineralogical Characteristics and Their Usability as Gemstones of Jaspers in Altered Metavolcanics Belonging to the Topçam Formation, Tokat, Turkiye

The jaspers located in the Topçam Mountain, Tepeyurt region (Tokat, Turkey), were formed at green-colored metavolcanic levels within Permian–Triassic schists. The sizes of the jaspers generally vary from a few cm to 1.5 m, and their colors vary from grayish–reddish–brownish/blackish tones depending on the increase in the amount of Fe and Mn elements they contain. According to thin section and X-ray Diffraction (XRD) analysis examinations, it was determined that the composition of jaspers includes quartz, hematite, calcite, and pyrite. As stated by the Wavelength Dispersive X-ray Fluorescence (WDXRF) analysis results, it was observed that the amount of SiO2 in jaspers was 82.5%, and the amount of Fe2O3 was 15.5%. According to Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) analysis results, Fe and Mn impurities, which are thought to cause the color of jaspers, as well as the amount of Fe (6975.5 ppm–46,893.9 ppm–96,431.1 ppm) and the amount of Mn (935.9–3219.7–6040.4 ppm), caused a darkening in color tones (grayish–reddish–brownish/blackish). Cabochon cutting applications were made of jaspers taken from the study area. As a result of these applications, it has been determined that jaspers can be used as gemstones due to their properties, such as their workability, polish retention, and color and light reflection.

ACCUMULATION OF HEAVY METALS IN APPLES AND PEARS FROM THE SUBURBS OF MITROVICA, KOSOVO

Intake of heavy metals through the food is a food safety problem that seriously affects consumer health. Therefore, information is needed on the intake of food contaminated with heavy metals and their concentrations, to assess the potential risk for human health. This paper aims to determine the accumulation of metals in apples and pears grown in the surroundings of Kosovska Mitrovica (Republic of Kosovo) and the bioconcentration factor (BF). With the help of the ICP-MS technique, were determined the amounts of Cu, Fe, Co, Mn, Ni, and Cr in apples and pears grown in three regions - Zvečan , Frashër, and Polski. From the conducted tests, the highest concentrations in apples and pears were determined for iron (on average 100.67 mg/kg for apples and 107.4 mg/kg for pears) and the lowest concentrations for cobalt (on average 0.13 mg/kg for apples and 0.18 mg/kg for pears). The lowest bioconcentration factor in apples is 0.01 (for Fe, Co, and Mn in all three regions), and the highest is 0.32 (for Cr in Zvečan). When determining the bioconcentration factor in pears, the lowest (0.01) was determined for iron (in all three regions) and manganese (in Zvečan and Frashër regions), and the highest bioconcentration factor was determined for copper – 0.46 (Polski region). There is a very high correlation between the values obtained for the analyzed metals in apples and pears. According to BF values, pears extract twice as much Cu and Co from the soil compared to apples, and the extraction of other metals from the soil is the same for both types of fruit.

Adapting the Mn content within a Fe-Mn-Si-based shape memory alloy by in situ parameter variations in laser-based additive manufacturing

Shape memory alloys exhibit unique properties ideal for functionally integrated components, such as actuators. While commonly used Ni-Ti alloys are well established, especially in biomedicine and aerospace, their high cost limits wider applications. Fe-based shape memory alloys present an affordable alternative, suitable for diverse applications, with a larger thermal hysteresis but lower recovery strain. Nonetheless, their functional properties can be enhanced through optimized processing methods like laser powder bed fusion and adjustments to their alloy composition. In the present study, laser powder bed fusion was used for modifying the composition and microstructure of a Fe-30Mn-6Si-5Cr alloy. For this purpose, laser parameters were varied to evaporate up to 47.3% of the initial Mn in the manufacturing process. In this context, the amount of Mn evaporated was dependent on both the line energy and more considerably on the volume energy density introduced in the manufacturing process. Subsequently, the impact of the resulting compositional changes on the microstructure was analyzed, and the functional properties were visualized using a demonstrator. Lowering the Mn content below 24.1% led to a higher degree of ferrite in the otherwise austenitic microstructure. This also affected the functional properties. These findings highlight the potential of laser-based additive manufacturing for modifying the composition and microstructure of shape memory alloys in situ and, thus, tailoring their functional properties.

Understanding the Role of Mn Substitution for Boosting High-Voltage Na4Fe3-xMnx(PO4)2P2O7 Cathode in Sodium-Ion Batteries.

Na4Fe3(PO4)2P2O7 is regarded as the most promising polyanionic cathode for sodium-ion batteries (SIBs) due to its superior structural stability, cost-effectiveness, and environmental benignity. However, the low operating voltage inevitably weakens its competitiveness in energy density. Previous works have tried to enhance its operating voltage by Mn doping, which draws on the design idea of LiFexMn1-xPO4 cathode for lithium-ion batteries, but with little success. In this context, uncovering the role of Mn substitution in Na4Fe3-xMnx(PO4)2P2O7 (NFMxPP) cathode is urgently needed. This work discloses the effect of Mn contents on the structure, sodium storage property, and reaction mechanism of NFMxPP cathode for the first time. Introducing a moderate amount of Mn (0.6 ≤ x ≤ 1.2) into NFMxPP can weaken the Fe-O bonding interaction, thus leading to the full utilization of Mn3+/Mn2+ redox couple. As the representative, NFM1.2PP cathode exhibited a high operating voltage of ≈3.3V with a reversible capacity of 109.2 mAh g-1. Note that a Hard carbon||NFM1.2PP full battery manifests considerably high-capacity retention of 92.3% over 1600 cycles. It is believed that an understanding of the role of Mn substitution in this work will promote the practical application of high voltage NFMxPP cathodes for SIBs.

Investigating Trace and Macro-element Composition of Herbal and Nutraceutical Dietary Supplements Marketed in Oman: Insights into Safety and Labeling.

With the global increase in the use of dietary supplements to provide nutrients in one's regular diet, these supplements' potential health risks and benefits have become a topic of significant interest. Interestingly, as dietary supplements, the Food and Drug Administration (FDA) in the United States (USA), Europe, and most countries do not require manufacturers and distributors to obtain approval or provide safety assessments before marketing those products. This research explores for the first time 16 heavy, trace and macro-elemental contents, namely, As, Ni, Cd, Pb, Cu, Co, Mn, Cr, Zn, V, Fe, Al, K, Na, Mg, and Ca, within 24 nutraceutical and herbal supplements marketed in Oman. The research is focusing on ensuring their compositions, concentrations, and freedom of toxic elements. ICP-OES was utilized, preceded by a microwave digestion technique to digest the samples in concentrated HNO3 and HCl (3:1, v/v). The method was validated within linear ranges of 0.03-5.00ppm and 1.0-200.0ppm for micro- and macro-elements, respectively, with %recoveries ranging from 90 to 104%. The limits of detection ranged from 0.01 to 0.09 and 0.14 to 0.30ppm, while the limits of quantification ranged from 0.03 to 0.28 and 0.46 to 0.91ppm for micro- and macro-elements, respectively. The detected levels were compared to online databases for risk assessment. Although As and Cd were not detected in all samples, Pb was found in nine samples, with some exceeding regulated limits of exposure. About 80% of the samples contained Al, of which two samples were susceptible to serious health risks of exceeding exposure limits in their compiled doses. The locally harvested Omani herbal supplements revealed significant amounts of Zn, Mg, Mn, and Cu. The results highlighted the potential risks associated with both dosage compliance and labeling discrepancies.

Enhancing the Performance of BaxMnO3 (x = 1, 0.9, 0.8 and 0.7) Perovskites as Catalysts for CO Oxidation by Decreasing the Ba Content.

Mixed oxides featuring perovskite-type structures (ABO3) offer promising catalytic properties for applications focused on the control of atmospheric pollution. In this work, a series of BaxMnO3 (x = 1, 0.9, 0.8 and 0.7) samples have been synthesized, characterized and tested as catalysts for CO oxidation reaction in conditions close to that found in the exhausts of last-generation automotive internal combustion engines. All samples were observed to be active as catalysts for CO oxidation during CO-TPRe tests, with Ba0.7MnO3 (B0.7M) being the most active one, as it presents the highest amount of oxygen vacancies (which act as active sites for CO oxidation) and Mn (IV), which features the highest levels of reducibility and the best redox properties. B0.7M has also showcased a high stability during reactions at 300 °C, even though a slightly lower CO conversion is achieved during the second consecutive reaction cycle. This performance appears to be related to the decrease in the Mn (IV)/Mn (III) ratio.

Quantifying Mixed Redox and Parasitic Processes in Li-Rich Disordered Rocksalt Li-Ion Battery Cathodes

Li-ion battery demand is expected to increase dramatically as the transportation and power generation sectors become electrified. To address the expense and scarcity of cobalt and nickel used in current layered cathodes, alternative transition metals must be explored. Disordered rocksalt (DRX) cathodes can be fully comprised of affordable, earth-abundant metals such as manganese and titanium and have shown high practical capacity but currently suffer from poor capacity retention and voltage fade [1]. Many researchers have attributed this to O redox, and the subsequent formation of deleterious reactive oxygen species, which can occur in DRX cathodes at states-of-charge as low as 40% [2,3]. Recently, researchers have increased the Mn content in DRX cathodes, with the intent of increasing Mn redox and suppressing O redox [4]. Furthermore, these Mn-rich DRX cathodes undergo a beneficial phase transformation upon electrochemical cycling, increasing capacity and almost eliminating voltage fade [4]. Yet, the redox contributions of Mn and O in these Mn-rich cathodes, especially after this phase transformation, are not understood.Here we decouple capacity contributions from Mn-redox, O-redox, and parasitic processes (e.g. electrolyte decomposition) for Mn-rich DRX using a combination of operando gas measurements and inductively coupled plasma – optimal emission spectrometry (ICP-OES). Mn-rich DRX cathodes were cycled to various states of charge in coin cells and the resulting Mn and O oxidation state were determined via titration mass spectrometry (TiMS) using oxalic acid and triflic acid, respectively. To account for lattice O2 loss, differential electrochemical mass spectrometry (DEMS) was used on select cells. To account for Mn dissolution during cycling, ICP-OES was used to quantify the amount of Mn remaining in the cathode as a function of cycle number. The results of this study provide insight into the various redox processes and interfacial degradation that occurs in DRX cathodes, thereby informing future design to improve high-voltage stability of these promising materials.[1]: Raphaële J. Clément et al 2020 Energy Environ. Sci. 2 345[2]: Tzu-Yang Huang et al 2023 Adv. Energy Mater. 13 2300241[3]: Roland Jung et al 2017 J. Electrochem. Soc. 164 A1361[4]: Zijian Cai et al 2023 Nat. Energy 1

Effect of Mo6+ induced valence changes of transition metal ions in Mn-rich layered cathode materials on electrochemical performance

Layered cathode materials for lithium-ion batteries have been extensively investigated; however, comparatively scant attention has been paid to Mn-rich layered cathode materials. Herein, LiNi0.5Mn0.5O2 cathode materials are doped to investigate the effect of doping elements on the electrochemical properties of Mn-rich layered cathodes. XRD (X-ray diffraction), XPS (X-ray photoelectron spectroscopy), and SQUID (superconducting quantum interference device) results reveal that Mo doping affects the electrochemical properties of the cathode materials by changing the valence state of transition metal ions. Due to the Mo6+ ions doping, a large proportion of Mn3+ ions present in LiNi0.5Mn0.5O2 were converted to Mn4+ ions, which alleviated the Jahn-Teller effect and reduced the elongated Mn-O octahedra, thus increasing the Li layer spacing and facilitating Li+ diffusion. Therefore, 1 % Mo-doped cathode exhibits a significantly improved Li-ion diffusion coefficient and superior rate performance with a specific discharge capacity of 103 mAh·g−1 at 5C. Meanwhile, the cathode materials significantly improve cycling performance due to the reduction in the amount of Mn3+. The current study provides guidelines for the modification of Mn-rich layered cathodes in the future.

3D Nickel–Manganese bimetallic electrocatalysts for an enhanced hydrogen evolution reaction performance in simulated seawater/alkaline natural seawater

In this paper, we report an inexpensive one-step synthesis of self-supported 3D nickel-manganese (NiMn) bimetallic coatings and their application for the hydrogen evolution reaction in simulated seawater (1 M KOH + 0.5 M NaCl) and alkaline natural seawater (1 M KOH + natural seawater). These binary coatings were electrodeposited on a titanium substrate using a facile electrochemical deposition method by a dynamic hydrogen bubble template technique. The as-deposited NiMn coatings with variable Mn amounts produce typical globular and unique porous architecture with abundant pores of different sizes. The activity of these fabricated catalysts towards the hydrogen evolution reaction was investigated by linear sweep voltammetry towards simulated seawater and alkaline natural seawater at different temperatures. The surface morphology and composition of the catalysts were also characterized by scanning electron microscopy and inductively coupled plasma optical emission spectroscopy. The as-prepared NiMn/Ti electrocatalyst, which was electrodeposited using a chemical bath containing Ni2+ and Mn2+ ions with a molar ratio of Ni2+:Mn2+ = 1:5, exhibits excellent hydrogen evolution activity in simulated seawater with an ultra-low overpotential of 64.2 mV to reach a current density of 10 mA cm−2. It is noteworthy that this NiMn/Ti electrocatalyst also achieves a current density of 10 mA cm−2 in alkaline natural seawater with a comparably low overpotential of 79.3 mV. The current densities increase by ca. 1.75–2.35 times with an increase in temperature from 25 °C to 75 °C for hydrogen evolution in both electrolytes. This bimetallic catalyst has shown excellent long-term stability at a constant potential of −0.23 V (vs. RHE) and a constant current density of 10 mA cm−2 for 10 h, which ensures higher durability and robustness for practical application of seawater splitting technology.

Total Polyphenol Contents and Mineral Profiles in Commercial Wellness Herbal Infusions: Evaluation of the Differences between Two Preparation Methods.

The popularity of the consumption of wellness herbal teas is due to the many health-promoting properties they seem to possess. Modern preparation methods using coffee machines are also popular today. Therefore, the purpose of this research was to evaluate differences in infusions obtained by the traditional method using filters and by espresso coffee machines using pods. In this regard, different herbal materials were selected and purchased in two different types of herbal containers, and the corresponding infusions were analyzed for the contents of total polyphenols and mineral elements. Results showed that filter infusions had higher polyphenol and mineral contents than pod infusions, excluding Cd and Pb. For each of the plant materials used, differences due to the method of infusion preparation are highlighted. From a qualitative point of view, both methods of infusion preparation are valid, but the filter infusion method allows a higher transfer of minerals and polyphenols into the infusion, improving quality. The analyzed infusions can be safely consumed with respect to As, Cd, Pb, and Hg contents. Good amounts of polyphenols and Mn can be obtained by drinking a cup of any of the infusions analyzed, especially the mate infusion obtained by the filter technique, with amounts of 429 mg for polyphenols and 69.27% of the RDA for manganese.

Potentially toxic metals in road dust: An assessment of ecological and health risks at Woldia and Kobo towns in North Wollo, Ethiopia

ABSTRACT The accumulation of heavy metals (HMs) in the environment threatens the ecosystem and human well-being. This study investigated the amounts of Mn, Fe, Ni, Co, Cu, Zn, Cd, Hg, Pb, As, and Cr, as well as the associated health and ecological risks. Thirty samples of roadside dust were collected in the northern Ethiopian towns of Woldia and Kobo. The collected samples were digested using acid digestion method and the levels of heavy metals were analysed using inductively coupled plasma optical emission spectroscopy. The results showed that the average concentrations of HMs were 0.103 (As)-7.6 (Cd) and 0.083 (Cd)-3.80 (Fe) mg/kg in Woldia and Kobo, respectively. All the HM concentrations investigated in this study were lower than the average global concentration, except for Hg in both towns and Cd in Woldia town. Analysis of variance (ANOVA) for the heavy metal concentration showed a significant difference across each sampling site, while Ni and Hg did not show a significant difference. The hazard quotient (HQ) and hazard index (HI) values of all HMs for adults and children through the three exposure routes were lower than 1, which means that they had a low likelihood of noncarcinogenic risks. The pollution index, geoaccumulation index, ecological risk index, integrated pollution index and risk index parameters were used to estimate the ecological risk. The results demonstrated that the pollution level mainly varied between low and moderate levels, except in Woldia, which is highly polluted by Cd metal that further detailed research is highly recommended to find out the sources of this metal.

Enhanced mineralization of bisphenol A by electric arc furnace slag: Fenton-like oxidation

Bisphenol A (BPA) aqueous solution was treated through a heterogeneous Fenton-like oxidation process with electric arc furnace slag (EAFS), a waste product from an Argentinian steel processing plant, as the catalyst. SEM/EDS, XRD, and Mössbauer spectroscopy characterization revealed a significant presence of Fe and minor amounts of Cu and Mn in EAFS, known to play active roles in the Fenton-like reactions. The predominant crystalline form of iron in EAFS was magnesiowüstite, accompanied by minor amounts of hematite, magnetite, maghemite, and metallic iron. Batch Fenton-like oxidation experiments were conducted under acidic conditions (pH 2.8–3), examining the effect of temperature (25, 50, and 70 °C) and catalyst load (0.1, 0.5, and 1 g/L) on BPA degradation and mineralization over 180 min. BPA was completely degraded within the first minutes, while mineralization levels improved from 40% to an outstanding 70% as the temperature increased from 25 to 70 °C. The catalyst gradually lost its activity after five cycles at 25 °C, but raising the temperature up to 70 °C allowed maintaining mineralization levels between 70 and 50% over ten cycles. The oxidation process involved a combined Fenton-like homogeneous/heterogeneous mechanism, and deactivation was linked to a lower leaching of active cations over the cycles, reduction of the Fe(II)/Fe(III) ratio in the iron phases, and blocking of active sites by adsorption of reaction intermediates. EAFS demonstrated an exceptional performance in the Fenton-like oxidation of BPA. The utilization of this type of industrial waste materials represents a promising technological alternative that could benefit both steel processing and water treatment plants.

Structural Evolution of Mn-Substituted FeOOH and Its Adsorption Mechanism for U(VI): Effect of the Mole Ratio of Mn/(Fe + Mn)

Mn-substituted FeOOH with different Mn/(Mn + Fe) molar ratios are synthesized, and characterized using FESEM, XRD, FTIR, ICP-OES, BET, Zeta potential, TG-DSC, XPS, and VSM. The results show that the actual doping amounts of Mn are 0%, 3.05%, 6.13%, 9.04%, 12.70%, and 15.14%, respectively. The substitution of Mn promotes the transformation of goethite from FeOOH to MnFe2O4, resulting in a saturation magnetization intensity of up to 14.90 emu/g for G-Mn15%, laying a theoretical foundation for magnetic recovery. The specific surface area of Mn-substituted FeOOH increases from 57.15 m2/g to 315.26 m2/g with an increasing Mn substitution amount. Combined with the abundant oxygen-containing functional groups such as -OH, Fe-O, and Mn-O on the surface, sufficient active sites are provided for the efficient adsorption of U(VI). The TG-DSC analysis results indicate that the substitution of Mn improves the thermal stability of goethite. In addition, XPS analysis results indicate that the substitution of Mn leads to the conversion of Fe3+ to Fe2+ in goethite, and the conversion of Mn2+ to Mn3+ replaces Fe3+ in the structure of goethite. Fe-O and Mn-O coordinate participate in the adsorption and reduction process of U(VI). The batch experiment results show that the substitution of Mn promotes the adsorption performance of goethite for U(VI). When T = 303 K, pH = 4.0, m/V = 0.5 g/L, and I = 0.01 mol/L NaCl, the maximum adsorption capacity of G-Mn15% for U(VI) is 79.24 mg/g, indicating the potential value of Mn substitution for goethite in the treatment of uranium-containing wastewater.

Total and Extractable Micronutrients in Tropical Acid Soils of Lampung, Indonesia

ABSTRACT The study aimed to determine the total and available amounts of iron (Fe), manganese (Mn), zinc (Zn), and copper (Cu) in the humid tropical acid soils of Lampung, Indonesia, and to identify the key factors affecting them. Topsoil samples were taken from 10 agricultural fields and 6 natural fields in 16 sub-districts of Lampung, Indonesia. The average total contents of Fe (26.36 g kg−1), Cu (8.97 mg kg−1), and Zn (53.24 mg kg−1) are generally below the world-soil average contents and those in other acid soils, which may be due to eluviation of Fe, Cu, and Zn into subsoil induced by high rainfall and the low natural contents of especially Cu and Zn in the parent rocks (acid volcanic rocks and sandstone). In contrast, the average total Mn content (1.20 g kg−1) is 2 to 8 times higher than that commonly found in acid soils and the world-soil average content, indicating that the parent materials may contain high Mn-bearing minerals. The total Fe, Mn, and Zn are positively correlated to the clay content, exchangeable-Ca and -Mg, and exchangeable-Mg, respectively, whereas the total Cu has no correlation to any soil properties. The amounts of available Fe, Mn, Cu, and Zn account for on average 0.38%, 6.20%, 21.50%, and 4.40% of the total contents, respectively. Around 6%, 12.5%, and 56% of the soil samples exhibit Mn, Cu, and Zn deficiency, respectively, and 25% face Fe toxicity. Total Fe and Mn are the main factors determining available Fe and Mn, respectively, whereas exchangeable-Mg and organic-C content mainly control available Cu and Zn, respectively.

Magnetic and dielectric properties of Mn2+ and Nb5+-doped NiCuZn ferrites for K-band junction circulators

Ni0.42-x/3Nbx/3Cu0.18Zn0.4MnxFe1.98−xO4−δ (x = 0–0.1) materials, possessing a high saturation magnetization, high dielectric constant, and narrow ferromagnetic resonance linewidth, were prepared via the solid-phase reaction method. The cation distribution, as well as the dielectric and gyromagnetic properties, were studied in detail. Mn2+ and Nb5+ incorporated in the lattice occupy tetrahedral site, causing the redistribution of cation and the reduction of A–B superexchange interaction. This leads to an increase in saturation magnetization followed by a decrease. The introduction of appropriate amounts of Mn2+ and Nb5+ ions reduces the magnetocrystalline anisotropy constant |K1| and thus reduces the ferromagnetic resonance linewidth (ΔH). Furthermore, high polarisability of Mn2+ and Nb5+ causes the increase in the dielectric constant of the ferrites. At x = 0.08, excellent gyromagnetic and dielectric properties, including a high dielectric constant (ε’ = 15.4@100 MHz), high saturation magnetization (4πMs = 4577 G), and narrow ferromagnetic resonance linewidth (ΔH = 129 Oe@9.55 GHz) for the NiCuZn ferrite, was achieved. Finally, a K-band microstrip circulator operating at 20.8 to 28 GHz was designed. The simulation showed that the isolation of the circulator in the working frequency band is greater than 20 dB, showing the potential of the prepared ferrites in microwave circulators.

Enhancing atomic ordering, magnetic and transport properties of Mn2VGa Heusler alloy thin films toward negatively spin-polarized charge injection

Magnetic materials with negative spin polarization have attracted attention for their potential to increase the design freedom of spintronic devices. This study investigated the effects of off-stoichiometry on the atomic ordering, microstructure, and magneto-transport properties in Mn2+xV1−xGa (x = −0.2, 0, +0.2, +0.4) Heusler alloy films, which are predicted to have large negative spin polarization derived from a pseudo band gap in the majority spin channel. The Mn2+xV1−xGa films epitaxially grown on MgO(001) substrates exhibits variations of B2 and L21 order with the Mn concentration. A high-quality L21 ordered film was achieved in the Mn-rich composition (x = +0.2) with B2 and L21 order parameters of 0.97 and 0.86, respectively, and a saturation magnetization of 1.4 μB/f.u., which agrees with the Slater-Pauling rule. Scanning transmission electron microscopy observations showed that B2 and L21 phases coexist in Mn-poor and stoichiometric films, while the L21 phase is dominant in the Mn-rich film with small amounts of Mn–V and Mn–Ga disorders, as revealed by laboratory and anomalous X-ray diffraction. Combined first-principles calculations and anisotropic magnetoresistance analysis confirms that the addition of excess Mn preserves the high spin polarization by suppressing the formation of detrimental antisites of V atoms occupying Mn sites. Therefore, the Mn-rich composition is promising for negatively spin-polarized charge injection in Mn2VGa-based spintronic applications.

The effect of heavy precipitation on the leaching of heavy metals from tropical coastal legacy tailings

The continued growth in demand for mineral resources has led to a large amount of mining wastes, which is a major challenge in the context of carbon neutrality and climate change. In this study, runoff migration, batch leaching, and column experiments were used to investigate the short-, medium-, and long-term leaching of heavy metals from legacy tailings, respectively; the cumulative metal release kinetic equations were established, and the long-term effects of tailings leaching were verified by HYDRUS-1D. In runoff migration experiments, surface dissolution of tailings and the co-migration of adsorbed soil particles by erosion were the main carriers in the early stages of leachate formation (Mn ∼ 65 mg/L and SO42- up to 2697.2 mg/L). Batch leaching tests showed that the concentration of heavy metals in soil leached by acid rain were 0.1 ∼ 22.0 μg/L for Cr, 0.7 ∼ 26.0 μg/L for Cu, 4.8 ∼ 5646.0 μg/L for Mn, 0.3 ∼ 232.4 μg/L for Ni, and 1.3 ∼ 448.0 μg/L for Zn. The results of column experiments indicated that some soluble components and metals with high mobility showed a significant decreasing trend at cumulative L/S ≤ 2. Additionally, the metals have higher leaching rates under TCLP conditions, as shown by Mn > Co > Zn > Cd > Ni > Cu > Pb > Cr. The fitting results of Langmuir equation were closer to the cumulative release of metals in the real case, and the release amounts of Mn, Zn, Co, and Ni were higher with 55, 5.84, 2.66, and 2.51 mg/kg, respectively. The water flow within tailings affects the spatial distribution of metals, which mainly exist in relatively stable chemical fractions (F3 + F4 + F5 > 90 %) after leaching. Numerical simulation verified that Mn in leachate has reached 8 mg/L at a scale of up to 100 years. The research results are expected to provide technical basis for realizing the resource utilization of tailings in the future.

Effect and mechanism of Mn2+ on urease activity during anaerobic biological treatment of landfill leachate.

As a crucial hydrolytic enzyme, urease plays a vital role in anaerobic biological treatment. It is well-known that manganese ions are abundant in landfill leachate, but their concentration fluctuates significantly. However, few studies have investigated the effect and mechanism of different concentrations of Mn2+ on urease activity during anaerobic biological treatment of landfill leachate. This paper aimed to investigate the effects and mechanisms of different concentrations of Mn2+ on urease activity. The results showed that an appropriate amount of Mn2+ could significantly enhance urease activity, while a high concentration of Mn2+ could inhibit it. Insight into the mechanisms behind this phenomenon, various methods such as Zeta potential, particle size, ultraviolet spectroscopy, fluorescence spectroscopy, Fourier transform infrared spectroscopy, and statistical analysis were employed in our study. Research suggested that, on one hand, Mn2+ may form hydrogen bonds with the side chain amino or carboxyl groups of urease amino acid residues, affecting the structure of urease through hydrogen bonding. Additionally, Mn2+ also binds to urease through hydrophobic interactions. On the other hand, the C-OH and C-N functional groups in urease have a strong affinity for Mn2+, and changes in these functional groups can greatly enhance the activity of urease. Furthermore, under the action of high concentrations of Mn2+, while the structure of urease becomes more stable, there is also a steric hindrance phenomenon that affects the substrate from entering the catalytic center. Therefore, studying the mechanism of Mn2+ affecting urease activity has significant biological significance and provides a new perspective for exploring the impact of metals on anaerobic bioprocessing of landfill leachate.

Influence of Mulberry Leaf Powder Additive on Chemical and Physical Characteristics of Wheat and Rice Flour Butter Cookies.

People of all age groups consume cookies every day. Consumers' preferences for cookies supplemented with functional plant raw materials have recently increased. Therefore, this research aimed to investigate the influence of a mulberry leaf additive on the proximate and mineral compositions, total phenolic and total chlorophyll content, antioxidant activity, and the hardness and color properties of butter cookies. Wheat and rice flour butter cookies were prepared by replacing the flour with mulberry leaf powder at 0, 4, 8, and 12% (w/w). The results revealed that the investigated chemical and physical characteristics of butter cookies depend on the flour used (rice or wheat) and the addition of mulberry leaf powder. Wheat and rice flour cookies with 12% mulberry leaf powder had the significantly highest contents of fiber (20.34 and 20.23%, respectively), ash (1.73 and 1.75%, respectively), K (170.22 and 160.22 mg 100 g-1, respectively), and Ca (170.45 and 160.68 mg 100 g-1, respectively). The rice flour cookies enriched with 12% leaf powder had the greatest amounts of total phenolics (1.48 mg 100 g-1), Zn (12.25 mg kg-1), Mn (6.28 mg kg-1), Cu (1.95 mg kg-1), and antioxidant activity (67.98%). However, the wheat cookies without mulberry leaf powder contained the most B (9.12 mg kg-1), while the no-added rice cookies contained the most Fe (14.30 mg kg-1). Replacing flour with leaf powder increased the cookies' hardness and decreased their lightness. In conclusion, enriching butter cookies with freeze-dried mulberry leaves can improve their nutritional value and antioxidant activity.

Distribution of trace and rare earth elements in the estuary of Ría de Huelva (SW Spain): Field data and geochemical modeling

The geochemistry of the Ría de Huelva estuary (Spain) has been widely studied owing to its unique conditions due to mixing of acid mine drainage (AMD), river water and seawater, which have been aggravated by the existence of an adjacent phosphate fertilizer plant and its associated phosphogypsum stack.To better understand the complex geochemistry of the overall estuarine system, we make use of (1) measured concentrations of relevant trace elements (rare earth elements (REEs) and metal(loid)s) in the sediments and waters of the estuary and (2) geochemical modeling which combines mixing and adsorption processes.Our study sheds light on the elemental distribution in the sediments and water in the water-mixing area. As seawater neutralizes the acidity of the river water (pH increases to 6.2) colloids of Fe- and Al-oxyhydroxysulphates (schwertmannite and basaluminite, respectively) precipitate as concentrations of aqueous Fe and Al increase. These phases have a high adsorption capacity and play a critical role in the geochemistry of the aquatic system by retaining Cu, Pb, Cr, As, P, REEs and smaller amounts of Zn, Co, Ni and Mn. The geochemical model reproduces the behaviour of the aqueous REEs, requiring high S/L ratios at pH ≥ 3.5 and participation of sediments and colloids in the reactions to match the field data.The evaluation of the effect of the adjacent phosphogypsum stack on the estuarine geochemistry shows that the stack has a notorious impact on the geochemistry of the surrounding estuarine environment owing to the release of high quantities of phosphate.