Magnetite recovery from copper tailings increases arsenic distribution in solution phase and uptake in native grass.

Reprocessing magnetite-rich copper (Cu) tailings prompted a concern about arsenic (As) risks in seepage water and revegetated plants at Ernest Henry Cu Mine (EHM) in North Queensland, Australia, due to the closely coupled relationship between iron (Fe) minerals and As mobility. The magnetite removal alone significantly decreased the content of crystalline Fe minerals and the maximum arsenate (As(V)) sorption capacity of the resultant tailings. A glasshouse experiment with native grass Red Flinders (Iseilema Vaginiflorum) was conducted with the reprocessed (low magnetite (LM)) and original (high magnetite (HM)) tailings, which were amended with 5% sugarcane residue (SR) as a basal treatment in combination with 0, 1 and 5% pine-biochar (BC). The organic matter treatments and plant growth stimulated the formation of secondary Fe minerals. The amount of extractable amorphous Fe in the amended and revegetated HM tailings was significantly higher than those in the LM. Arsenic forms in the specifically sorbed and the sorbed by amorphous Fe oxides were significantly increased by the SR amendment in the LM tailings, but which were decreased in the HM, compared to the unamended tailings. Soluble As levels in the porewater of the LM under revegetation were significantly higher (300-1150 µg As L-1) than those (up to 45-90 µg As L-1) in HM tailings in the same treatment, which led to the higher As concentrations in the plants grown in the LM tailings. In particular, root As concentration (62-146 mg kg-1) in the LM tailings was almost a magnitude higher than those (8-17 mg kg-1) in the HM. The present results confirmed the initial expectation that the recovery of magnetite from the Cu tailings significantly elevated the risk of As solubility in the tailings by decreasing As sorption capacity and increasing soluble As levels. Thus, it would be beneficial to retain high contents of magnetite in the top layer (e.g., root zone) of the Cu tailings for managing As risk and revegetation in the future.

Co-ordinated functions of Mms proteins define the surface structure of cubo-octahedral magnetite crystals in magnetotactic bacteria.

Magnetotactic bacteria synthesize magnetosomes comprised of membrane-enveloped single crystalline magnetite (Fe3 O4 ). The size and morphology of the nano-sized magnetite crystals (< 100 nm) are highly regulated and bacterial species dependent. However, the control mechanisms of magnetite crystal morphology remain largely unknown. The group of proteins, called Mms (Mms5, Mms6, Mms7, and Mms13), was previously isolated from the surface of cubo-octahedral magnetite crystals in Magnetospirillum magneticum strain AMB-1. Analysis of an mms6 gene deletion mutant suggested that the Mms6 protein plays a major role in the regulation of magnetite crystal size and morphology. In this study, we constructed various mms gene deletion mutants and characterized the magnetite crystals formed by the mutant strains. Comparative analysis showed that all mms genes were involved in the promotion of crystal growth in different manners. The phenotypic characterization of magnetites also suggested that these proteins are involved in controlling the geometries of the crystal surface structures. Thus, the co-ordinated functions of Mms proteins regulate the morphology of the cubo-octahedral magnetite crystals in magnetotactic bacteria.

Thermostable trypsin conjugates immobilized to biogenic magnetite show a high operational stability and remarkable reusability for protein digestion.

In this work, magnetosomes produced by microorganisms were chosen as a suitable magnetic carrier for covalent immobilization of thermostable trypsin conjugates with an expected applicability for efficient and rapid digestion of proteins at elevated temperatures. First, a biogenic magnetite was isolated from Magnetospirillum gryphiswaldense and its free surface was coated with the natural polysaccharide chitosan containing free amino and hydroxy groups. Prior to covalent immobilization, bovine trypsin was modified by conjugating with α-, ß- and γ-cyclodextrin. Modified trypsin was bound to the magnetic carriers via amino groups using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and N-hydroxysulfosuccinimide as coupling reagents. The magnetic biomaterial was characterized by magnetometric analysis and electron microscopy. With regard to their biochemical properties, the immobilized trypsin conjugates showed an increased resistance to elevated temperatures, eliminated autolysis, had an unchanged pH optimum and a significant storage stability and reusability. Considering these parameters, the presented enzymatic system exhibits properties that are superior to those of trypsin forms obtained by other frequently used approaches. The proteolytic performance was demonstrated during in-solution digestion of model proteins (horseradish peroxidase, bovine serum albumin and hen egg white lysozyme) followed by mass spectrometry. It is shown that both magnetic immobilization and chemical modification enhance the characteristics of trypsin making it a promising tool for protein digestion.

Magnetite biomineralization in Magnetospirillum gryphiswaldense: time-resolved magnetic and structural studies.

Magnetotactic bacteria biosynthesize magnetite nanoparticles of high structural and chemical purity that allow them to orientate in the geomagnetic field. In this work we have followed the process of biomineralization of these magnetite nanoparticles. We have performed a time-resolved study on magnetotactic bacteria Magnetospirillum gryphiswaldense strain MSR-1. From the combination of magnetic and structural studies by means of Fe K-edge X-ray absorption near edge structure (XANES) and high-resolution transmission electron microscopy we have identified and quantified two phases of Fe (ferrihydrite and magnetite) involved in the biomineralization process, confirming the role of ferrihydrite as the source of Fe ions for magnetite biomineralization in M. gryphiswaldense. We have distinguished two steps in the biomineralization process: the first, in which Fe is accumulated in the form of ferrihydrite, and the second, in which the magnetite is rapidly biomineralized from ferrihydrite. Finally, the XANES analysis suggests that the origin of the ferrihydrite could be at bacterial ferritin cores, characterized by a poorly crystalline structure and high phosphorus content.

Purification and magnetic interrogation of hybrid Au-Fe3O4 and FePt-Fe3O4 nanoparticles.

Purifying heterodimers: differential magnetic catch and release separation is used to purify two important hybrid nanocrystal systems, Au-Fe(3)O(4) and FePt-Fe(3)O(4). The purified samples have substantially different magnetic properties compared to the as-synthesized materials: the magnetization values are more accurate and magnetic polydispersity is identified in morphologically similar hybrid nanoparticles.

Layer-by-layer assembled Fe3O4@C@CdTe core/shell microspheres as separable luminescent probe for sensitive sensing of Cu2+ ions.

A novel multifunctional microsphere with a fluorescent CdTe quantum dots (QDs) shell and a magnetic core (Fe(3)O(4)) has been successfully developed and prepared by a combination of the hydrothermal method and layer-by-layer (LBL) self-assembly technique. The resulting fluorescent Fe(3)O(4)@C@CdTe core/shell microspheres are utilized as a chemosensor for ultrasensitive Cu(2+) ion detection. The fluorescence of the obtained chemosensor could be quenched effectively by Cu(2+) ions. The quenching mechanism was studied and the results showed the existence of both static and dynamic quenching processes. However, static quenching is the more prominent of the two. The modified Stern-Volmer equation showed a good linear response (R(2) = 0.9957) in the range 1-10 µM with a quenching constant (K(sv)) of 4.9 × 10(4) M(-1). Most importantly, magnetic measurements showed that the Fe(3)O(4)@C@CdTe core/shell microspheres were superparamagnetic and they could be separated and collected easily using a commercial magnet in 10 s. These results obtained not only provide a way to solve the embarrassments in practical sensing applications of QDs, but also enable the fabrication of other multifunctional nanostructure-based hybrid nanomaterials.

Magnetic Fe3O4 nanoparticles for adsorptive removal of acid dye (new coccine) from aqueous solutions.

The ability of magnetic Fe3O4 nanoparticles (MFN) to remove new coccine (NC), an acidic dye, from aqueous solutions was studied. Parameters including ionic strength, pH, and temperature were evaluated. MFN, prepared by precipitation method, exhibits an average particle size of 12.5 nm, specific surface area of 85.5 m²/g, and pH(zpc) of 5.9. Results of kinetic adsorption experiments indicated that the pseudo-second-order rate of adsorption increased with increasing initial NC concentration. Findings also revealed that the equilibrium data could be fitted into Langmuir adsorption isotherm. The adsorption is favored at low pH, high temperature, and low ionic strength, whereupon a maximum adsorption capacity of 1.11 x 10⁻4 mol/g was determined for NC. Thermodynamic functions indicated that the adsorption process is spontaneous and exothermic in nature. Tests of regeneration showed that after 5 regeneration cycles the adsorption capacity of NC decreased to 35% to its original capacity.

Magnetic iron compounds in the human brain: a comparison of tumour and hippocampal tissue.

Iron is a central element in the metabolism of normal and malignant cells. Abnormalities in iron and ferritin expression have been observed in many types of cancer. Interest in characterizing iron compounds in the human brain has increased due to advances in determining a relationship between excess iron accumulation and neurological and neurodegenerative diseases. In this work, four different magnetic methods have been employed to characterize the iron phases and magnetic properties of brain tumour (meningiomas) tissues and non-tumour hippocampal tissues. Four main magnetic components can be distinguished: the diamagnetic matrix, nearly paramagnetic blood, antiferromagnetic ferrihydrite cores of ferritin and ferrimagnetic magnetite and/or maghemite. For the first time, open hysteresis loops have been observed on human brain tissue at room temperature. The hysteresis properties indicate the presence of magnetite and/or maghemite particles that exhibit stable single-domain (SD) behaviour at room temperature. A significantly higher concentration of magnetically ordered magnetite and/or maghemite and a higher estimated concentration of heme iron was found in the meningioma samples. First-order reversal curve diagrams on meningioma tissue further show that the stable SD particles are magnetostatically interacting, implying high-local concentrations (clustering) of these particles in brain tumours. These findings suggest that brain tumour tissue contains an elevated amount of remanent iron oxide phases.

An integrated electro-chemical and natural treatment system for industrial water pollution control.

Experiments were conducted to test the feasibility of applying an integrated electro-chemical (EC) and natural treatment system for treatment of some industrial wastewaters. The EC process was found to be very effective in removing lead, a model heavy metal from some wastewaters. Within 20 minutes of operation time, 5 to 10 A of electric current and specific surface area of electrode of 46.51 m2/m3, the lead concentrations in the wastewaters were reduced from 35-100 mg/l to less than 1 mg/l. Based on a kinetic model developed from the experimental data, the important parameters for the EC process were found to be electric current, specific surface area of electrode, and operation time. From scanning electron microscopic and X-ray diffractometric (XRD) analysis, the EC sludge samples were found to compose mainly of maghemite (Fe2O3), magnetite (Fe3O4), and laurionite (PbClOH), suitable for disposal to secure landfills. Two pilot-scale constructed wetlands (CW) in series, a model natural treatment system, were employed to treat wastewaters of an industrial estate in Thailand. At organic loading rates of 57-140 kg BOD/hectare-year, these constructed wetlands were able to reduce BOD from 90 to 4 mg/l, while suspended solids, total nitrogen and total phosphorus were reduced from 100 to 10 mg/l, 24 to 4.6 mg/l and 7 to 1.5 mg/l, respectively, during the summer season. These results demonstrated technical feasibility of CW in removing organic and other pollutants contained in this industrial wastewater.