Ratio Of Manganese Research Articles

Mitigating excessive heat in Arabica coffee using nanosilicon and seaweed extract to enhance element homeostasis and photosynthetic recovery.

Global warming-related temperature increases have a substantial effect on plant and human health. The Arabica coffee plant is susceptible to growing in many places across the world where temperatures are rising. This study examines how nanosilicon and seaweed extracts can improve Arabica coffee plant resilience during heat stress treatment (49.0 ± 0.3°C) by maintaining mineral homeostasis and photosynthetic ability upon recovery. The principal component analysis arrangement of four treatments, nanosilicon (Si), seaweed extract (SWE), Si + SWE, and control (CT), showed each element ratio of magnesium, phosphorus, chloride, potassium, manganese, iron, copper, and zinc per silicon in ambient temperature and heat stress that found influenced upper shoot rather than basal shoot and root within 74.4% of largest feasible variance as first principal component. Magnesium and iron were clustered within the silicon group, with magnesium dominating and leading to a significant increase (p ≤ 0.05) in magnesium-to-silicon ratio in the upper shoot under heat conditions, especially in Si and Si + SWE treated plants (1.11 and 1.29 fold over SWE treated plant, respectively). The SWE and Si + SWE treated plants preserved chlorophyll content (15.01% and 28.67% over Si-treated plant, respectively) under heat stress, while the Si and Si + SWE treated plants restored photosynthetic efficiency (Fv/Fm) better than the SWE treated plant. The concomitant of the Si + SWE treatment synergistically protected photosynthetic pigments and Fv/Fm by adjusting the magnesium-silicon homeostasis perspective in Arabica coffee to protect real-world agricultural practices and coffee cultivation under climate change scenarios.

A hydrothermal plume on the Southwest Indian Ridge revealed by a multi-proxy approach: Impact on iron and manganese distributions (GEOTRACES GS02)

Iron (Fe) and manganese (Mn) are crucial micronutrients that limit oceanic primary productivity in the Southern Ocean. It has been recently suggested that hydrothermal activity may be an important source of oceanic dissolved iron, yet, this contribution is still not fully understood and only one active hydrothermal site has been reported on the Southwest Indian Ridge (SWIR), south of 40°S.Using a multi-proxy approach, this study demonstrates the occurrence of hydrothermal venting on the SWIR in the near vicinity of the location 44°51.690 S, 36°10.460 E, which is likely to be a low or moderately high temperature fluid. Indeed, we report high values of dissolved methane to manganese ratios (up to 11.1 ± 1.2 mol mol−1), low particulate iron (pFe) and manganese (pMn) concentrations (with maximum values of 0.7 nmol L−1 and 0.06 nmol L−1, respectively) associated with the presence of few oxyhydroxides, as well as high 223Radium (Ra) and 224Ra activities near the seafloor. The Fe and Mn data revealed a significant enrichment at depths influenced by hydrothermal circulation on the seafloor, within the Upper Circumpolar Deep Water. Dissolved Fe (dFe) and dissolved Mn (dMn) concentrations were enriched by 3- and 7-fold, respectively, and pFe and pMn by 2- and 1.5-fold, respectively, compared to a reference station located outside the SWIR. They were however lower than concentrations reported so far near high temperature vents, suggesting a weaker influence of this hydrothermal system on deep Fe and Mn reservoirs. We show that a large fraction of the dFe could be stabilized by organic complexation with humic substances (eHS, estimated 27–60% of dFe). High prokaryotic abundance related to the proximity of the hydrothermal vent suggests that other Fe-complexing ligands of biological origin might also stabilize Fe in its dissolved form. Collectively, these measurements integrated within the concept of a “multi-proxy approach”, helped painting a more detailed picture of the complex interactions and processes in this region of the SWIR. Although the system is a source of both dFe and dMn to the deep ocean, the low current velocities and the bathymetry likely limit the fertilization of surface water by dFe and dMn along this section of the SWIR.

A multi-metric approach to characterize variability in Yellow Perch (Perca flavescens) use of Lake Ontario and two barrier-protected coastal wetlands

Yellow Perch (Perca flavescens) inhabit both nearshore and coastal wetland habitats of the Laurentian Great Lakes throughout their lifetime and are known to exhibit different movement life histories. However, uncertainty persists in the spatial extent of this variation and in the duration of habitat use. To explore these uncertainties, we used a multi-metric approach that included water and otolith microchemistry and tissue stable isotope ratios (δ13C, δ15N). The ratio of manganese to calcium in otoliths was used to identify transitional movements between nearshore Lake Ontario and wetland habitats while carbon and nitrogen tissue isotope ratios revealed variable duration of wetland inhabitance. Our research suggests that the multi-metric approach was useful for addressing questions that could not be answered by one method alone. Our results demonstrate individual differences in duration of coastal wetland habitat residence among Yellow Perch, which may influence their susceptibility to recreational harvest. As Yellow Perch are an important species of consideration for management agencies such as the Great Lakes Fishery Commission, exposing such diversity is important when considering the potential for differential contributions of individuals with variable movement life histories to overall population stability and resilience over time.

Unravelling the role of iron and manganese oxides in colouring Late Antique glass by micro-XANES and micro-XRF spectroscopies

This research aims to understand colouring technologies in 5th–7th centuries glass imported to Atlantic Britain by correlating the iron (Fe) and manganese (Mn) ratios and oxidation states with colour. Despite having a similar matrix chemical composition and concentrations of Fe and Mn oxides, these vessels display different colours (from green to yellow/amber, sometimes with purple streaks). Colour changes can be induced by controlling the reduction-oxidation reactions that occur during glass production, which are influenced by the raw materials, furnace and melt atmosphere, and recycling. To evaluate these parameters, reference glasses were prepared, following the composition of Late Antique archaeological glass recovered from Tintagel (UK) and Whithorn (UK). A corpus of archaeological and experimental glass samples was analysed using bulk Fe and Mn K-edge x-ray absorption near edge structure (XANES) spectroscopy, micro-XANES and micro x-ray fluorescence (μ-XRF) at beamline ID21, at the European Synchrotron Radiation Facility. Fe and Mn XANES spectra of the archaeological glass indicate that Fe and Mn are in a similar oxidation state in all the yellow samples, predominantly Fe3+ and Mn2+. No detectable difference in Mn and Fe oxidation state occurs in the purple streaks compared to the yellow glass bulk but μ-XRF maps of the distribution of Fe and Mn show that Mn is more concentrated in the purple streaks. This indicates that the purple colour of the streaks is mainly due to a higher Mn/Fe ratio and persistence of more oxidised manganese in the purple areas, even though it is difficult to detect. Many archaeological fragments appear pale green in transmitted light but amber in reflected light. XANES studies detected the presence of surface layers where manganese is more oxidised. This layer is believed to scatter transmitted and reflected light differently and might be responsible for the optical features of the archaeological glass.

Efficient toluene degradation using Bacillus subtilis biofilm-supported Mn–Ce/zeolite catalysts

This study investigated a new approach for synthesizing Bacillus subtilis biofilm-supported Mn–Ce/zeolite catalysts for the degradation of gaseous toluene. Four different metal oxide nano-catalysts (ZMn, ZMnCe-10%, ZMnCe-20%, and ZMnCe-30%) were synthesized with varying ratios of manganese (Mn) and cerium (Ce) on zeolite nanoparticles. TEM, SEM, XRD, BET, XPS, and EDX mapping were used to examine these four samples, as well as simple zeolite. Based on these analyses, the catalytic activity of the prepared samples ZMn, ZMnCe-10%, ZMnCe-20%, and ZMnCe-30% for the complete oxidation of toluene and toluene intermediate products were tested with Non-thermal plasma (NTP) technology in a dielectric barrier discharge (DBD) reactor. Among all, ZMnCe-20% showed the highest toluene degradation efficiency (89%) at low concentrations (200 ​ppm) and humidity (>50%). Later, highly efficient and hydrophobic nano-biocatalysts were prepared by combining B. subtilis biofilm wild-type (WT) and engineered B. subtilis biofilm EPS with ZMnCe-20% catalyst. EPS is the main component found in biofilm matrix and plays a key role in influencing properties such as biofilm stability, electron transfer, surface roughness and hydrophobicity. Compared to WT B. subtilis biofilm, EPS overexpressed B. subtilis biofilm showed stronger growth and development on ZMnCe-20% nanocatalyst. Moreover, the NTP system packed with ZMnCe-20%/biofilm (EPS+) nano-biocatalyst exhibited the highest toluene degradation activity (99%) with (83%) CO2 selectivity, (up to 50%) reduction in NOx concentration and complete ozone decomposition at (250 ​ppm) toluene concentrations and increased humidity (>90%). High-energy electrons generated in the NTP system break the C–H and C–C bond between the rings of the toluene molecule, forming several byproducts which are later reacted with active radical species such as O, OH, and O3 and further converted into final degradation products (CO2 and H2O). The results demonstrated successful biofilm development and growth on the ZMnCe-20% catalyst with advanced features such as superhydrophobicity, H2O resistance, improved surface roughness, and electron generation. In short, the study's approach combines bioengineering and material science to develop sustainable nano-biocatalysts for removing VOCs in industrial and environmental settings.

Catalytic activation of peroxodisulfate using shape-controlled cerium-manganese composite oxide for phenol degradation: Kinetics and degradation pathway investigation

Phenol-containing wastewater is typical organic wastewater, and its treatment is arduous. An advanced method to treat this type of wastewater is persulfate activation. Environmentally friendly cerium-manganese composite oxide materials were synthesized by hydrothermal method and applied to the phenol degradation process. Various ratios of cerium and manganese, as well as the amount of sodium hydroxide, were investigated. The solid solutions of cerium and manganese were formed and confirmed by X-ray diffraction (XRD) and transmission electron microscopy (TEM). H2-temperature programmed reduction (H2-TPR) and X-ray photoelectron spectroscopy (XPS) were utilized to analyze the synergistic effect of cerium and manganese. It is found that there is a transformation between Ce4+/Ce3+ and Mn2+/Mn3+, which makes the material more trivalent manganese and thereby increases the catalytic activity. The effect of materials in catalyzing phenol degradation by peroxodisulfate (PDS) under various preparation conditions is discussed and high-efficiency removal of phenol can be achieved and the removal rate at 180 min is close to 100%. The kinetic of this process was investigated and activation energy of phenol degradation is 62.35 kJ/mol. The degradation pathway of phenol was studied and it is found that PDS can be activated by low metal ions and the ·OH and SO4·– radicals play crucial roles according to the quenching experiments.

Synergistic mechanism of iron manganese supported biochar for arsenic remediation and enzyme activity in contaminated soil

This study prepared and characterized bamboo-derived biochar loaded with different ratios of iron and manganese; evaluated its remediation performance in arsenic-contaminated soil by studying the changes in various environmental factors, arsenic speciation, and arsenic leaching amount in the soil after adding different materials; proposed the optimal ratio and mechanism of iron–manganese removal of arsenic; and explained the multivariate relationship between enzyme activity and soil environmental factors based on biological information. Treatment with Fe–Mn-modified biochar increased the organic matter, cation exchange capacity, and N, P, K, and other nutrient contents. During the remediation process, O-containing functional groups such as Mn–O/As and Fe–O/As were formed on the surface of the biochar, promoting the transformation of As from the mobile fraction to the residual fraction and reducing the phytotoxicity of As, and the remediation ability for As was superior to that of Fe-modified biochar. Mn is indispensable in the FeMn-BC synergistic remediation of As, as it can increase the adsorption sites and the number of functional groups for trace metals on the surface of biochar. In addition to electrostatic attraction, the synergistic mechanism of ferromanganese-modified biochar for arsenic mainly involves redox and complexation. Mn oxidizes As(Ⅲ) to more inert As(V). In this reaction process, Mn(Ⅳ) is reduced to Mn(Ⅲ) and Mn(II), promoting the formation of Fe(Ⅲ) and the conversion of As into Fe–As complexes, while As is fixed due to the formation of ternary surface complexes. Moreover, the effect of adding Fe–Mn-modified biochar on soil enzyme activity was correlated with changes in soil environmental factors; catalase was correlated with soil pH; neutral phosphatase was correlated with soil organic matter; urease was correlated with ammonia nitrogen, and sucrase activity was not significant. This study highlights the potential value of FM1:3-BC as a remediation agent in arsenic-contaminated neutral soils.

Investigation of the beneficiation of refractory ferromanganese ores “Zhomart” deposits

In order to provide ferroalloy production with high-quality raw materials, the need to develop technologies for processing of low-grade manganese and ferromanganese ores is becoming increasingly important. In view of the change in the quality characteristics of ores, the decrease in manganese content and the ability to beneficiation by traditional methods, it is necessary to consider new approaches and technological solutions. The article presents data from a study on the beneficiation of refractory iron-manganese ore from the Zhomart deposit. The mineralogy, physical and mechanical properties, and granulometric composition of the ore were determined. The results of a study on gravitational beneficiation using a laboratory pulsator with a pneumatic drive and a laboratory 2-chamber diaphragm jigging machine and magnetic beneficiation of ore with a high-intensity magnetic field are presented. Iron-containing concentrate (Fe-45% and Mn-6.5% is mainly represented by hematite mixed with non-metallic minerals quartz and calcite) and iron-manganese concentrate (Mn-21.7% and Fe-21.1% in the form of hematite, Brownite and pyrolusite, also mixed with quartz and calcite). The concentrates are not suitable for smelting manganese-containing ferroalloys but can be used in the process of electrothermal beneficiation with selective carbothermal reduction of iron in an ore-thermal furnace. The smelting products can be manganese cast iron and iron-free, low-phosphorus limiting manganese slag with a high ratio of manganese to iron.

Lithium isotope composition of Ediacaran dolostones from the Nuccaleena and Doushantuo formations

The end of the Cryogenian glaciations undoubtedly affected the chemistry of the Neoproterozoic oceans, with potential consequences for the evolution of life; the duration and extent of this influence are poorly constrained. Lithium (Li) isotopes in carbonates can be used to investigate past weathering events and riverine input into the oceans. Here, we report the Li isotope (δ7Li) composition of the Ediacaran cap dolostones (Marinoan) from the Nuccaleena Formation, South Australia and the Doushantuo Formation, South China to investigate changes in weathering during the aftermath of the Marinoan glaciation. The origin of dolomite formation is still hotly debated, and the inability to precipitate dolomite at ambient temperatures (the ‘dolomite problem’) has not yet been resolved. The dominant hypothesis for the presence of marine dolomite is that it is of secondary origin, owing to diagenetic replacement of calcium carbonate, but a second hypothesis is that it forms as a result of primary marine deposition; both are plausible hypotheses. Using carbon isotopes (δ13C) and ratios of manganese and strontium (Mn/Sr), we suggest that diagenesis may not have significantly altered the δ7Li composition of the primary dolomite, but this cannot be discounted without further diagenetic modelling. As a result, we cannot infer the δ7Li composition of the Ediacaran oceans, as further work must be done to address the impact of diagenesis on the δ7Li values. Nevertheless, this dataset contributes to a Li isotope chemostratigraphic record of the Proterozoic, which is a key element to understanding the emergence of complex life.

One-pot solvothermal synthesis of highly dispersed, morphology- and crystal structure-tunable copper-manganese oxide for catalytic combustion of toluene at low temperatures

Copper-manganese composite oxide (CuMnOx) catalyst was prepared through an improved solvothermal reduction by short-chain dopamine (DA) with catechol structure for catalytic oxidation of toluene. The catalyst possessed the properties of controllable morphology, adjustable size, high dispersion and excellent catalytic activity. The regular hexagonal, square and spherical crystal particles with different crystal structures were synthesized by adjusting the molar ratio of copper and manganese during the reaction. Further investigation of the performance indicated that CuMnOx − 1 (Cu:Mn = 1:1) had high catalytic combustion activity with low temperatures of T50 (205 ℃) and T90 (221 ℃). Meantime, it has favorable stability with the basically unchanged conversion efficiency in 60 h of continuous testing.

ІMPACT OF THE NATURE OF ELECTRICALLY CONDUCTIVE IMPURITY ON CAPACITIVE PROPER­TIES AND RESISTANCE TO CURRENT LOADS OF CATHODE MATERIALS BASED ON LiMn2O4

The impact of the nature of electrically conductive graphite and graphene admixtures in spinel LiMn2O4 with different degrees of dispersion, composition and morphology on the surface element distribution and the cycling ability under current loads from 0.5 to 8 C of composite cathode materials based on such spinels have been studied by the methods of electron microscopy, X-ray spectrometry, the BET method and galvanostatic-potentiostatic cycling. The specific surface of graphene structures was studied, which was 23 m2/g for G-N and 27.7 m2/g for G-H2O, and the porosity was about 100 nm for the above samples. It was established that the degree of dispersion of spinel affects not only the morphology of the surface of the electrodes, but also the distribution of elements, primarily manganese and oxygen, which take part in electrode redox reactions, as well as the content of the carbon component. Using the elemental analysis of the component composition of the surface, the ratio of manganese to oxygen was calculated, and it was shown that in samples with graphite, manganese is in a more reduced state, and the maximum oxidized state of manganese is observed in samples with graphene, which was synthesized from an aqueous medium. In the case of finely dispersed spinel, the dependence of the carbon content and the ratio of manganese to oxygen on the surface has an antibate character relative to samples with coarsely dispersed spinel and correlates with the number of meso­pores on the surface. The dependence of the degree of dispersion and the oxidation state of manganese is in good agreement with the dependence of specific capacity on the discharge current density for composite electrodes. In XDM spinel with graphene synthesized from an aqueous medium, the obtained capacitive characteristics exceed the other characteristics of the materials by 20%. It has been experimentally proven that by changing the nature of the impurity and the degree of dispersion of the spinel, it is possible to adjust the capacitive properties and resistance to current loads of composite electrodes.

Optimization of Mn‐Mg‐Al Mixed Oxides Composition on their Activity towards the Total Oxidation of Aromatic and Oxygenated VOCs

AbstractA series of mixed oxides (Mn‐Mg‐Al) is prepared by coprecipitation via a hydrotalcite route with different manganese ratios. Structural, textural, and redox properties are studied by XRD, N2‐sorption, H2‐TPR, and XPS techniques. MnxMg6‐xAl2‐O mixed oxides (with 0≤x≤6) are tested in the total oxidation of ethanol and toluene, two probe molecules representing respectively oxygenated and aromatic VOCs. Catalysts with higher manganese contents have shown the best catalytic performance for the oxidation of both ethanol and toluene. The surface activity of the materials is mainly related to the presence of manganese species in three different oxidation states (+II, +III, and +IV) in the bulk and on the material's surface. Since high Mn‐content catalysts showed similar physicochemical properties and catalytic activity, Mn4Mg2‐O is selected as the optimal composition of these materials. Furthermore, its aging test is compared to that of noble metal‐based commercial catalysts (Pd/γ‐Al2O3).

Impact of the Yellow River capture on the paleoenvironmental changes of Hongze Lake, China

The Yellow River (YR) capture of the Huai River had a profound effect on the landscape evolution, ecology, and social development in China, disrupting the evolution of some vital shallow floodplain lakes. Because of the absence of lacustrine sediment provenance analysis, previous studies were inadequate in distinguishing the influence of YR capture on paleoenvironmental changes in these lakes, especially on landscape evolution, redox conditions, lake level changes, and organic productivity. The current study aims to use X-ray fluorescence-core scanning (XRF-CS) and multivariate statistics on a 9.8 m sediment core from Hongze Lake (HZL), China, to analyze the impact of the YR capture on the lake's paleoenvironmental changes and the sediment provenance simultaneously. High-resolution images, magnetic susceptibility, and XRF-based multi-element data were obtained using a GEOTEK Multi-Sensor Core Logger. The calcium (Ca) content indicates the presence of YR sediment in HZL, given the high Ca content in YR sediment and the identification of mainly exogenous sources of Ca in HZL. The high values of Ca indicate that 48.7% of the sediment in the center of HZL is related to the YR's incursion. Periods of higher Ca content coincide with periods of higher oxygenation levels of the lake (as indicated by the ratio of manganese to titanium) and lower organic content in the lake sediment (as indicated by the ratio of incoherent to coherent scatter). These analyses reveal that the YR's capture of HZL significantly increased the lake's oxygen level. Furthermore, the decrease in the organic content of sediment tends to be the result of the accelerated deposition caused by the YR. The decrease in Ca content coincides with an increase in lake levels (as indicated by magnetic susceptibility). Thus, it can be inferred that the embankment on the eastern side of HZL, built to increase lake storage, has reduced the incursion frequency of the YR.

Kinetically inert manganese (II)-based hybrid micellar complexes for magnetic resonance imaging of lymph node metastasis.

The localization and differential diagnosis of the sentinel lymph nodes (SLNs) are particularly important for tumor staging, surgical planning and prognosis. In this work, kinetically inert manganese (II)-based hybrid micellar complexes (MnCs) for magnetic resonance imaging (MRI) were developed using an amphiphilic manganese-based chelate (C18-PhDTA-Mn) with reliable kinetic stability and self-assembled with a series of amphiphilic PEG-C18 polymers of different molecular weights (C18En, n = 10, 20, 50). Among them, the probes composed by 1:10 mass ratio of manganese chelate/C18En had slightly different hydrodynamic particle sizes with similar surface charges as well as considerable relaxivities (∼13 mM-1 s-1 at 1.5 T). In vivo lymph node imaging in mice revealed that the MnC MnC-20 formed by C18E20 with C18-PhDTA-Mn at a hydrodynamic particle size of 5.5 nm had significant signal intensity brightening effect and shortened T1 relaxation time. At an imaging probe dosage of 125 μg Mn/kg, lymph nodes still had significant signal enhancement in 2 h, while there is no obvious signal intensity alteration in non-lymphoid regions. In 4T1 tumor metastatic mice model, SLNs showed less signal enhancement and smaller T1 relaxation time variation at 30 min post-injection, when compared with normal lymph nodes. This was favorable to differentiate normal lymph nodes from SLN under a 3.0-T clinical MRI scanner. In conclusion, the strategy of developing manganese-based MR nanoprobes was useful in lymph node imaging.

Continuous Flow Epoxidation of Alkenes Using a Homogeneous Manganese Catalyst with Peracetic Acid.

Epoxidation of alkenes is a valuable transformation in the synthesis of fine chemicals. Described herein are the design and development of a continuous flow process for carrying out the epoxidation of alkenes with a homogeneous manganese catalyst at metal loadings as low as 0.05 mol%. In this process, peracetic acid is generated in situ and telescoped directly into the epoxidation reaction, thus reducing the risks associated with its handling and storage, which often limit its use at scale. This flow process lessens the safety hazards associated with both the exothermicity of this epoxidation reaction and the use of the highly reactive peracetic acid. Controlling the speciation of manganese/2-picolinic acid mixtures by varying the ligand:manganese ratio was key to the success of the reaction. This continuous flow process offers an inexpensive, sustainable, and scalable route to epoxides.

The Influence of Cerium to Manganese Ratio and Preparation Method on the Activity of Ceria-Manganese Mixed Metal Oxide Catalysts for VOC Total Oxidation

A set of ceria-manganese mixed metal oxide catalysts with varying Ce:Mn ratios were prepared by coprecipitation using sodium carbonate and were evaluated for the total oxidation of propane and naphthalene. Manganese-rich samples were the most active, with Ce0.25Mn0.75Ox having the highest activity. Catalysts were characterised using X-ray diffraction, Brunauer–Emmett–Teller (BET) surface area, Raman spectroscopy, temperature programmed reduction (TPR), electron microscopy, and X-ray photoelectron spectroscopy (XPS), establishing that the high activity of Ce0.25Mn0.75Ox was due to the formation of phase-separated Mn-substituted ceria and Mn2O3 phases that were not simultaneously present in the other catalysts. The catalyst preparation technique for the most active ratio was investigated using co-precipitation by urea, oxalic acid and citric acid, and mechanochemical grinding. For propane, the mechanochemical and urea catalysts were more active than the carbonate coprecipitated catalyst, due to greater surface area and increased phase separation. This work demonstrates that ceria-manganese mixed metal oxides are more active than the parent oxide, but that preparation technique is also important for controlling activity.

Preparation and investigation of the structural and optical characteristics of manganese- doped cadmium oxide films

In this paper, undoped and Mn-doped CdO thin films deposited on the glass substrates by the chemical spray pyrolysis method (CSP) technique. The prepared thin films characterized by XRD, AFM, FESEM and UV visible. The results of the X-ray diffraction patterns revealed that the prepared films have a polycrystalline structure and a cubic structure. The crystallite size (D) value for all prepared films was calculated using Scherrer's method, Williamson-Hall method and size strain plot (SSP) method, from the results, it was observed that, the crystallite size decreases with increase in doping ratio of Manganese. The optical propertis show that with an increase in Mn concentration, the CdO films' transparency and the energy gap of the films increases. The Hall effect measurement revealed that all prepared films have negatives type (n-type) charge carriers, the value of the doping ratio rises, the Hall coefficient decreases.

Three-dimensional ordered macroporous cerium–manganese composite oxide for NO oxidation

Three-dimensional ordered microporous cerium–manganese composite oxide catalysts with different cerium–manganese ratios were prepared by a sol–gel method for NO oxidation and soot combustion.

Association Between the Ratios of Selenium to Several Elements and Mild Cognitive Impairment in the Elderly.

To investigate the relationship between the correlation ratios of selenium (Se) and other elements and mild cognitive impairment (MCI) among older adults. A total of 1000 individuals participated in our research analysis. The concentrations of elements in whole blood were determined using inductively coupled plasma mass spectrometry to reflect their exposure levels. Participants' cognitive function was assessed using the Mini-Mental State Examination. Logistic regression analysis was used to evaluate the relationship between elemental ratios and MCI. Se concentration was positively correlated with red blood cell count (r = 0.219, p < 0.001), haemoglobin level (r = 0.355, p < 0.001), haematocrit (r = 0.215, p < 0.001), mean corpuscular haemoglobin (r = 0.294, p < 0.001) and mean corpuscular haemoglobin concentration (r = 0.428, p < 0.001) and negatively correlated with red cell volume distribution width-standard deviation (r = -0.232, p < 0.001) and platelet distribution width (r = -0.382, p < 0.001). Compared with the normal group, the ratios of Se/vanadium (V), Se/lead (Pb) and Se/cadmium (Cd) in the whole blood of the MCI group were significantly lower (all p < 0.001), while the ratios of manganese (Mn)/Se and iron (Fe)/Se were higher (all p < 0.001). The increase in the ratios of Se/V, Se/Pb and Se/Cd is related to a decreased risk of MCI among older adults; contrarily, an increase in the ratios of Mn/Se and Fe/Se may be a risk factor for MCI.

Preparation of H1.6Mn1.6O4/Chitosan Composite Microsphere and Its Adsorption Properties of Lithium

AbstractLi1.6Mn1.6O4 was synthesized by soft chemical synthesis and solid‐phase calcination. Then it was compounded with chitosan (CTS) to form composite microsphere by Epichlorohydrin used as a cross‐linking agent. Subsequently, 0.5 mol ⋅ L−1 sodium persulfate was used as an eluent, and the lithium ion sieve adsorbent (H1.6Mn1.6O4) was prepared. The influencing factors of the preparation conditions for the lithium ion sieve precursor were investigated, and the results showed that when the mixed salt solution was 100 mL (molar ratio of lithium manganese for 4 : 1), added 5 mL H2O2 and calcined at 400 °C for 5 hours, the relatively pure Li1.6Mn1.6O4 could be obtained. Aimed at the composite microsphere, the influencing factors of its preparation conditions was investigated. The results showed that the ratio of CTS to lithium ion sieve powder was 1 : 2, the amount of cross‐linking agent was 2 mL and the time were 30 min was the best condition. The adsorption effect was tested by eluting Li1.6Mn1.6O4 and composite microsphere with a variety of eluents. The results showed that the adsorption effect of Li1.6Mn1.6O4 was best when 0.5 mol ⋅ L−1 hydrochloric acid was used as the eluent, and its adsorption capacity was 32.34 mg ⋅ g−1, the dissolution loss rate of Mn is 1.61 %; the composite microsphere had the best effect when 0.5 mol ⋅ L−1 sodium persulfate was used as the eluent, its adsorption capacity was 13.29 mg ⋅ g−1, the dissolution loss rate of Mn was only 0.91 %, moreover it had better repeatability, with only a 20.83 % drop in performance after the tenth runs. Ion selectivity experiments showed that the adsorption selection was in the order of Li+≫K+&gt;Mg2+&gt;Ca+&gt;Na+, and the composite adsorbent was highly selective for Li+.