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The occurrence of manganese in groundwater causes coloured water and pipe rusting in water treatment systems. Consumption of manganese-contaminated water promotes neurotoxicity in humans and animals. Manganese-oxidizing bacteria were isolated from contaminated areas in Thailand for removing manganese from water. The selected bacterium was investigated for its removal kinetics and mechanism using synchrotron-based techniques. Among 21 isolates, Streptomyces violarus strain SBP1 (SBP1) was the best manganese-oxidizing bacterium. At a manganese concentration of 1 mg L -1 , SBP1 achieved up to 46% removal. The isolate also successfully removed other metal and metalloid, such as iron (81%) and arsenic (38%). The manganese concentration played a role in manganese removal and bacterial growth. The observed self-substrate inhibition best fit with the Aiba model. Kinetic parameters estimated from the model, including a specific growth rate, half-velocity constant, and inhibitory constant, were 0.095 h -1 , 0.453 mg L -1 , and 37.975 mg L -1 , respectively. The synchrotron-based techniques indicated that SBP1 removed manganese via combination of bio-oxidation (80%) and adsorption (20%). The study is the first report on biological manganese removal mechanism using synchrotron-based techniques. SBP1 effectively removed manganese under board range of manganese concentrations. This result showed the potential use of the isolate for treating manganese-contaminated water.

Manganese-oxidizing bacteria have been widely investigated for bioremediation of Mn-contaminated water sources and for production of biogenic Mn oxides that have extensive applications in environmental remediation. In this study, a total of 5 Mn-resistant bacteria were isolated from river water and investigated for Mn removal. Among them, Ochrobactrum sp. NDMn-6 exhibited the highest Mn removal efficiency (99.1%). The final precipitates produced by this strain were defined as a mixture of Mn 2 O 3 , MnO 2 , and MnCO 3 . Optimal Mn-removal performance by strain NDMn-6 was obtained at a temperature range of 25-30 °C and the salinity of 0.1-0.5%. More interestingly, strain NDMn-6 could be resistant to salinities of up to 5%, revealing that this strain could be possibly applied for Mn remediation of high salinity regions or industrial saline wastewaters. This study also revealed the potential of self-detoxification mechanisms, wherein river water contaminated with Mn could be cleaned by indigenous bacteria through an appropriate biostimulation scheme.

Incorporation of dual functions, i.e., sensing and adsorption, into one single organic-inorganic hybrid material for the detection and removal of toxic permanganate (MnO 4 - ) ions is of great importance, representing a challenging and new task in the design and application of new functional materials. However, most of the reported materials display only one function as either sensing probes or adsorbents. In this work, a fluorescent cuboid mesoporous silica-based hybrid material (SiO 2 @SFNO) is first prepared by the covalent coupling of a new safranin O-based fluorophore (2,8-dimethyl-5-phenyl-3,7-bis(3-(3-(triethoxysilyl)propyl)ureido)phenazin-5-ium chloride) (SFNO) and newly-made cuboid mesoporous silica, which showed selective dual-functional activities towards MnO 4 - and green emission at 575 nm with a long-range excitation wavelength that is suitable for bio-imaging application. The design of this SiO 2 @SFNO material is based on the position of -NHCONH- groups, which are mainly responsible for the strong and selective coordination with MnO 4 - . SiO 2 @SFNO is responsive to MnO 4 - at parts per billion (67 ppb) level; it also displays high adsorption ability (292 mg g -1 ) to MnO 4 - in aqueous solutions. The fluorescence responses of MnO 4 - in vivo (limnodrilus claparedianus and zebrafish) demonstrate the possibility of further application in biology. Interestingly, this SiO 2 @SFNO material is also capable of monitoring trace amounts of Hg 2+ and Cu 2+ in living organisms, holding great potential in bio-related applications.

The study combined activated carbon with a rotating biological contactor. The activated carbon adsorption experiments were conducted and the biofilm was formed by using the river water directly. The effects of different hydraulic retention times on the removal of NH 4 + -N, TP, and permanganate index and on the biofilm properties were investigated at the optimum rotational speed of the disc. Experimental results are as follows. The Freundlich isotherm showed that activated carbon had better adsorption properties for NH 4 + -N, TP, and permanganate index in water.When the disk speed was 3 r·min -1 , the removal efficiency was the best, and the removal rates of NH 4 + -N, TP and permanganate index were the best at 86.05%, 81.28%, and 77.09%, respectively. In addition, there was a significant linear correlation between the hydraulic retention time and the removal of NH 4 + -N and TP ( R 2 >0.9), respectively. The removal rates of NH 4 + -N and TP at different hydraulic retention times were significantly different ( P <0.05), but the permanganate index was not ( P >0.05).Hydraulic retention time had effects on the biofilm activity, protein and polysaccharide contents,and the three-dimensional fluorescence peaks of S-EPS, LB-EPS, and TB-EPS of the biofilm.

In order to study the purifying effect of combined floating bed constucted by salinity plant Suaeda salsa and microorganisms on the slightly salt-alkaline water, blank floating bed A, S.salsa floating bed B, microbes floating bed C and S.salsa + microorganisms combined floating bed D were established, and slightly salt-alkaline eutrophic water body (pH 8.5-9.0, salinity 5‰-7‰) was purified under continuous flow conditions in the laboratory. Results showed that the removal rates of total nitrogen, total phosphorus, permanganate index by S.salsa floating bed were 32.5%, 14.3% and 28.2%, respectively. And the removal rates of total nitrogen, total phosphorus and permanganate index by S.salsa + microorganisms combined floating bed D which installed artificial medium with microorganisms reached 70.5%, 34.7% and 70.8%, respectively, of which the removal rates of total nitrogen, total phosphorus and permanganate index by microbial units were 37.7%, 21.6% and 44.5%, respectively. Synergies removal rates of nitrate nitrogen and total nitrogen by S.salsa + microorganisms combined floating bed were 12.2% and 0.3%, but there was no synergy in the process of removing ammonia nitrogen, total phosphorus and permanganate index, which indicated that the synergies of S.salsa and microorganisms in the combined floating bed were suppressed in slightly salt-alkaline environment. The high-throughput sequencing technique was adopted to analyze the microbial community in the floating bed C and D, which indicated that the abundance and diversity of microbial community in the combined floating bed were higher, and this was consistent with the result of the higher removal rate of the flotation bed D. Principal component analysis showed that the microbial degradation was a major factor in reducing the concentration of pollutants. This study provided a guide for the using of floating bed in purifying slightly salt-alkaline eutrophic water bodies in coastal area.

Manganese-oxide minerals (MnO x ) are widely distributed over the Earth's surface, and their geochemical cycling is globally important. A multicopper oxidase (MCO) MnxG protein from marine Bacillus bacteria plays an essential role in producing MnO x minerals by oxidizing Mn 2+ (aq) at rates that are 3 to 5 orders of magnitude faster than abiotic rates. The MnxG protein is isolated as part of a multiprotein complex denoted as "Mnx" that includes accessory protein subunits MnxE and MnxF, with an estimated stoichiometry of MnxE 3 F 3 G and corresponding molecular weight of ≈211 kDa. Herein, we report successful expression and isolation of the MCO MnxG protein without the E 3 F 3 hexamer. This isolated MnxG shows activity for Mn 2+ (aq) oxidation to form manganese oxides. The complement of paramagnetic Cu(II) ions in the Mnx protein complex was examined by electron paramagnetic resonance (EPR) spectroscopy. Two distinct classes of type 2 Cu sites were detected. One class of Cu(II) site (denoted as T2Cu-A), located in the MnxG subunit, is identified by the magnetic parameters g ∥ = 2.320 and A ∥ = 510 MHz. The other class of Cu(II) sites (denoted as T2Cu-B) is characterized by g ∥ = 2.210 and A ∥ = 615 MHz and resides in the putative hexameric MnxE 3 F 3 subunit. These different magnetic properties correlate with the differences in the reduction potentials of the respective Cu(II) centers. These studies provide new insights into the molecular mechanism of manganese biomineralization.

Eggshell membrane (ESM) is selected as biotemplate to prepare MnO2 submicroparticles (SMPs) using Chinese Brush with sodium hydroxide solution. The size with average 710 nm of the obtained materials is in good consistency with the microsructured biotemplate. An efficient and convenient absorbent for methylene blue (MB) is developed. The removal efficiency could reach up to 93% in 35 min under room temperature without pH adjusting owing to the excellent adsorption from ESM itself and hydroxyl group formed on the surface of MnO2 crystal in the aqueous solution. Materials on the membrane can be separated from the wastewater simply to avoid the secondary pollution caused by the leak of material. This interesting approach to MnO2 SMPs and facile operation for MB adsorption could open a new path to the submicro-materials based wastewater treatment.

A three-dimensional water-stable cationic metal-organic framework (MOF) pillared by a neutral ligand and with Ni(II)  metal nodes has been synthesized employing a rational design approach. Owing to the ordered arrangement of the uncoordinated tetrahedral sulfate (SO4 (2-) ) ions in the channels, the compound has been employed for aqueous-phase ion-exchange applications. The compound exhibits rapid and colorimetric aqueous-phase capture of environmentally toxic oxoanions (with similar geometries) in a selective manner. This system is the first example of a MOF-based system which absorbs both dichromate (Cr2 O7 (2-) ) and permanganate (MnO4 (-) ) ions, with the latter acting as a model for the radioactive contaminant pertechnetate (TcO4 (-) )., (© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

MnS is a p-type semiconductor with both antiferromagnetism and wide band gap, endowing it potential applications for short wavelength optoelectronic devices, solar cells and luminescent materials. Despite successful biosynthesis of nano CdS, PbS and ZnS with extremely low solubility product, there have been no reports available on biosynthesis of nano MnS so far because both PO4(3-) and OH(-) negatively disturb reaction between Mn(2+) and S(2-) through forming Mn3(PO4)2 and Mn(OH)2 as undesirable impurities. In this work, high-purity MnS nanocrystals were synthesized in presence of newly isolated Clostridiaceae sp. through strictly controlling pH value and PO4(3-) dose for the first time. The results showed that hexagonal-shaped γ-MnS with a diameter of 2-3 μm and a thickness of 200-300 nm was obtained by biosynthesis at 0.014 g/L PO4(3-) dose and pH 5.8. The hexagonal-shaped particle possessed dense and uniform texture. The γ-MnS had an obvious absorption peak at 325 nm and an emission peak at 435 nm as well as paramagnetic property with a coercivity of 52.91 Oe and a retentivity of 4.37 × 10(-3) emu/g at ambient temperature. The studies demonstrated that biosynthesis was qualified for preparation of nano metal sulfites with relatively high solubility product like MnS, widening its application spectrum.

High purity electrolytic manganese dioxide (EMD) is the main raw material used for manufacturing of zinc and manganese based portable batteries (alkaline with manganese AlMn and zinc carbon Zn-C). Lately, due to the progressive depletion of MnO(2) natural resources, the quantity of artificially electrolytic produced MnO(2) has started to increase to satisfy the demand. This paper describes an electrolytic process for the simultaneous production of the following components:The electrolysis process was conducted in a specialized laboratory facility. The study was particularly focused on the following electrolysis process parameters:, (Copyright © 2013 Elsevier Ltd. All rights reserved.)

Manganese, in the form of oxide, was recovered from spent alkaline and zinc-carbon batteries employing a biohydrometallurgy process, using a pilot plant consisting in: an air-lift bioreactor (containing an acid-reducing medium produced by an Acidithiobacillus thiooxidans bacteria immobilized on elemental sulfur); a leaching reactor (were battery powder is mixed with the acid-reducing medium) and a recovery reactor. Two different manganese oxides were recovered from the leachate liquor: one of them by electrolysis (EMO) and the other by a chemical precipitation with KMnO4 solution (CMO). The non-leached solid residue was also studied (RMO). The solids were compared with a MnOx synthesized in our laboratory. The characterization by XRD, FTIR and XPS reveal the presence of Mn2O3 in the EMO and the CMO samples, together with some Mn(4+) cations. In the solid not extracted by acidic leaching (RMO) the main phase detected was Mn3O4. The catalytic performance of the oxides was studied in the complete oxidation of ethanol and heptane. Complete conversion of ethanol occurs at 200°C, while heptane requires more than 400°C. The CMO has the highest oxide selectivity to CO2. The results show that manganese oxides obtained using spent alkaline and zinc-carbon batteries as raw materials, have an interesting performance as catalysts for elimination of VOCs., (Copyright © 2013 Elsevier Ltd. All rights reserved.)

Zinc sorption on sheathed Leptothrix discophora bacterium, the isolated extracellular polymeric substances (EPS) sheath, and Mn oxide-coated bacteria was investigated with macroscopic and spectroscopic techniques. Complexation with L. discophora was dominated by the outer membrane phosphoryl groups of the phospholipid bilayer while sorption to isolated EPS was dominated by carboxyl groups. Precipitation of nanoparticulate Mn oxide coatings on the cell surface increased site capacity by over twenty times with significant increase in metal sorption. XAS analysis of Zn sorption in the coated system showed Mn oxide phase contributions of 18 to 43% through mononuclear inner-sphere complexes. The coordination environments in coprecipitation samples were identical to those of sorption samples, indicating that, even in coprecipitation, Zn is not incorporated into the Mn oxide structure. Rather, through enzymatic oxidation by L. discophora, Mn(II) is oxidized and precipitated onto the biofilm providing a large surface for metal sequestration. The nanoparticulate Mn oxide coating exhibited significant microporosity (75%) suggesting contributions from intraparticle diffusion. Transient studies conducted over 7 months revealed a 170% increase in Zn loading. However, the intraparticle diffusivity of 10(-19) cm(2) s(-1) is two orders of magnitude smaller than that for abiotic Mn oxide which we attribute to morphological changes such as reduced pore sizes in the nanoparticulate oxide. Our results demonstrate that the cell-bound Mn oxide particles can sorb significant amounts of Zn over long periods of time representing an important surface for sequestration of metal contaminants.

Filtration experiments were conducted to investigate soluble manganese removal in granular media filtration; sand, manganese oxide coated sand (MOCS), sand + MOCS (1:1) and granular activated carbon (GAC) were used as filter media. Manganese removal, manganese oxide accumulation, turbidity removal, and regeneration of MOCS under various conditions were examined. Soluble manganese removal by the MOCS column was rapid and efficient; most of the removal happened at the top (e.g. 5 cm) of the filter. When filter influent with an average manganese concentration of 0.204 mg l(-1) was fed through the filter columns, the sand + MOCS and MOCS columns removed 98.9% and 99.2% of manganese, respectively. However, manganese removal in sand and the GAC columns was not significant during the initial stage of filtration, but after eight months of filter run they could remove 99% and 35% of manganese, respectively. It was revealed that partial replacement of sand with MOCS showed comparable manganese removal to that of the MOCS filter media.

Transmission electron microscopy (TEM) techniques were used to investigate the spent cathodic material of a single common brand of disposable alkaline batteries. Mn-oxide particles are anhedral and irregular in shape and compose an estimated 99-95% of the < 10 microm size fraction of sample material. Diameters of particles vary widely and typically are between 50 nm and 3 microm; however, most particles are approximately 200-400 nm in diameter. Chemical composition varies for Mn-oxide particles with concentrations being SiO2 (0.00-1.52 wt%), TiO2 (0.49-4.58 wt%), MnO (65.85-92.06 wt%), ZnO (1.00-7.53 wt%), K2O (4.97-20.48 wt%) and SO3 (0.43-2.21 wt%). Discrete prismatic zinc crystals occur and vary from a maximum of approximately 0.8 microm long x 0.15 microm wide, to 100 nm long x 20 nm wide. Titanium metal was also observed in samples and composes approximately 0.25-1.0% of the < 10 microm size fraction of sample material. Results of this study suggest that battery components may be recycled in some special applications. Examples are low energy-low material requirement products such as paint pigments and Zn nanoparticles. This investigation provides detailed constraints on the nature of spent cathodic materials to improve existing recycling methods and develop new technologies.

We investigated the production of manganese (Mn) oxides using repeated-batch bioreactors maintained over long periods under laboratory conditions. Freshwater epilithic biofilms were used as the initial inocula. The bioreactors yielded suspended solids that could remove 0.1 mM dissolved Mn(II) within a few days. Chemical titration, X-ray absorption near-edge structure spectroscopy, and X-ray diffraction analysis revealed that the Mn(II) had been converted to poorly crystallized layer-type Mn(IV) oxides, which were similar to known biogenic Mn oxides from pure bacterial cultures. Spherical or rod-shaped Mn microconcretions occurred in the suspended solids; transmission electron microscopy showed that these structures likely resulted from the microbial activity but not represent living cells. Instead, the presence of encapsulated, sheathed, and hyphal budding cells in the suspended solids indicated that a range of Mn-depositing bacteria contributed to the Mn oxide formation. To our knowledge, our data represent the first observation of production of such Mn oxides in a laboratory microcosm wherein a range of Mn-depositing bacteria coexist. The fact that sorption of trace Zn(II) and Ni(II) ions onto the suspended solids co-occurred with the removal of dissolved Mn(II) emphasizes the important role of Mn-oxidizing microorganisms in the fates of trace or contaminant metals in the aquatic environment.

The neurotoxic effects of manganese (Mn) at elevated concentrations are well known. This raises the question, which of the Mn species can cross neural barriers and appear in cerebrospinal fluid (CSF). CSF is the last matrix in a living human organism available for analysis before a compound reaches the brain cells and therefore it is assumed to reflect best the internal exposure of brain tissue to Mn species. A previously developed CE method was modified for separation of albumin, histidine, tyrosine, cystine, fumarate, malate, inorganic Mn, oxalacetate, alpha-keto-glutarate, nicotinamide-dinucleotide (NAD), citrate, adenosine, glutathione, and glutamine. These compounds are supposed in the literature to act as potential Mn carriers. In a first attempt, these compounds were analyzed by CZE-UV to check whether they are present in CSF. The CZE-UV method was simpler than the coupled CZE-inductively coupled plasma (ICP)-dynamic reaction cell (DRC)-MS method and it was therefore chosen to obtain a first overview information. In a second step, the coupled method (CZE-ICP-DRC-MS) was used to analyze, in detail, which of the compounds found in CSF by CZE-UV were actually bound to Mn. Finally, 13 Mn species were monitored in CSF samples, most of them being identified: Mn-histidine, Mn-fumarate, Mn-malate, inorganic Mn, Mn-oxalacetate, Mn-alpha-keto glutarate, Mn-carrying NAD, Mn-citrate and Mn-adenosine. By far the most abundant Mn species was Mn-citrate showing a concentration of 0.7 +/- 0.13 microg Mn/L. Interestingly, several other Mn species can be related to the citric acid cycle.

Sequential extractions of metals can be useful to study metal distributions in various soil fractions. Although several sequential extraction procedures have been suggested in the literature, most were developed for temperate soils and may not be suitable for tropical soils with high contents of Mn and Fe oxides. The objective of this study was to develop a sequential fractionation procedure for Cu and Zn in tropical soils. Extractions were performed on surface (0-20 cm) samples of ten representative soils of Sao Paulo State, Brazil. Chemically reactive Mn forms were satisfactorily assessed by the new modified procedure. Amorphous and crystalline Fe oxides were more selectively extracted in a new two-step extraction. Soil-born Zn and Cu were primarily associated with recalcitrant soil fractions. The proposed procedure provided more detailed information on metal distribution in tropical soils and better characterization of the various components of the soil matrix. The new procedure is expected to be an important tool for predicting the potential effects of environmental changes and land application of metals on the redistribution of chemical forms of metals in tropical soils.

Manganese is a trace element known to activate many enzymes involved in metabolic processes and it shows protective function against oxidative stress. On the other hand, increased Mn levels are known for damaging the central nervous system, resulting in motoric abnormalities and psychic disorder. Such additional Mn exposure can cause an "Mn overflow" in the liver, accompanied by production of specific (labile) Mn transporters (Mn-species). The speciation of these Mn-compounds is still unknown but they are believed targeting the brain. The aim of this paper was to develop a speciation method for manganese species in liver extracts, which allows to speciate the compounds quickly and with minimal risk of species alteration. Capillary electrophoresis (CE)-inductively coupled plasma mass spectrometry (ICP-MS) offers a valuable tool as analytes are not in contact to a stationary phase which probably affects species stability. Separation usually is fast and ICP-MS detection is element specific and sensitive. The paper describes the set-up and optimization of the hyphenated technique, optimization of separation according to pH and finally the Mn speciation of a liver extract. Several Mn species were found, such as arginase, Mn-transferrine, Mn-albumine and some more. The detection limit of the method was determined at 1.1 microg Mn/L independent on the species.

The syntheses and properties of the monomeric [MnIII/IIH31(OH)]-/2- and [MnIIIH31(O)]2- complexes are reported, where [H31]3- is the tripodal ligand tris[(N'-tert-butylureaylato)-N-ethyl)]aminato. Isotope-labeling studies with H218O confirmed that water is the source of the terminal oxo and oxygen in the hydroxo ligand. The molecular structures of the [MnIIH31(OH)]2- and [MnIIIH31(O)]2- complexes were determined by X-ray diffraction methods and show that each complex has trigonal bipyramidal coordination geometry. The MnIII-O distance in [MnIIIH31(O)]2- is 1.771(4) A, which is lengthened to 2.059(2) A in [MnIIH31(OH)]2-. Structural studies also show that [H31]3- provides a hydrogen-bond cavity that surrounds the MnIII-O(H) units. Using a thermodynamic approach, which requires pKa and redox potentials, bond dissociation energies of 77(4) and 110(4) kcal/mol were calculated for [MnIIH31(O-H)]2- and [MnIIIH31(O-H)]-, respectively. The calculated value of 77 kcal/mol for the [MnIIH31(O-H)]2- complex is supported by the ability of [MnIIIH31(O)]2- complex to cleave C-H bonds with bond energies of <80 kcal/mol.