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Sample records for cholorotoxin-conjugated iron oxide

  1. Rapid pharmacokinetic and biodistribution studies using cholorotoxin-conjugated iron oxide nanoparticles: a novel non-radioactive method.

    Directory of Open Access Journals (Sweden)

    Michelle Jeung-Eun Lee

    Full Text Available BACKGROUND: Recent advances in nanotechnology have led to the development of biocompatible nanoparticles for in vivo molecular imaging and targeted therapy. Many nanoparticles have undesirable tissue distribution or unacceptably low serum half-lives. Pharmacokinetic (PK and biodistribution studies can help inform decisions determining particle size, coatings, or other features early in nanoparticle development. Unfortunately, these studies are rarely done in a timely fashion because many nanotechnology labs lack the resources and expertise to synthesize radioactive nanoparticles and evaluate them in mice. METHODOLOGY/PRINCIPAL FINDINGS: To address this problem, we developed an economical, radioactivity-free method for assessing serum half-life and tissue distribution of nanoparticles in mice. Iron oxide nanoparticles coated with chitosan and polyethylene glycol that utilize chlorotoxin as a targeting molecule have a serum half-life of 7-8 hours and the particles remain stable for extended periods of time in physiologic fluids and in vivo. Nanoparticles preferentially distribute to spleen and liver, presumably due to reticuloendothelial uptake. Other organs have very low levels of nanoparticles, which is ideal for imaging most cancers in the future. No acute toxicity was attributed to the nanoparticles. CONCLUSIONS/SIGNIFICANCE: We report here a simple near-infrared fluorescence based methodology to assess PK properties of nanoparticles in order to integrate pharmacokinetic data into early nanoparticle design and synthesis. The nanoparticles tested demonstrate properties that are excellent for future clinical imaging strategies and potentially suitable for targeted therapy.

  2. Iron Oxides

    Energy Technology Data Exchange (ETDEWEB)

    Qafoku, Nikolla; Amonette, James E.

    2016-09-19

    Abstract: Fe oxides are common clay-sized oxide, oxyhydroxide and hydroxide soil minerals. They are compounds of Fe, O, and H that have structures based on close-packed arrays of O. The octahedral and tetrahedral cavities within these arrays are filled with either Fe3+ or Fe2+ to form Fe(O/OH)6, FeO6, or FeO4 structural units. All of the naturally occurring Fe oxide minerals usually undergo some degree of isomorphous substitution of other metal ions for Fe in their structures. Relatively simple techniques may be used to identify Fe oxides in the field based on their typical colors and magnetic properties. In the laboratory, a variety of instrumental techniques can be used to confirm phase identity and to quantify amount. Of these, X-ray diffraction, infrared spectroscopy, electron microscopy, thermal analysis, and Mössbauer spectroscopy are the most commonly used techniques. As oxides, the functional groups on their surfaces may have positive, negative, or no charge depending on pH and on the concentration and nature of other ions in the contact solution. A net positive surface charge usually is observed in soils because Fe oxides have a point-of-zero-charge in the neutral or slightly basic pHs. The functional groups on the surface form complexes with cations and anions from the aqueous phase. Their sorption and electron-buffering properties significantly affect the geochemical cycles of almost all elements having agronomic or environmental significance.

  3. Iron oxide surfaces

    Science.gov (United States)

    Parkinson, Gareth S.

    2016-03-01

    The current status of knowledge regarding the surfaces of the iron oxides, magnetite (Fe3O4), maghemite (γ-Fe2O3), haematite (α-Fe2O3), and wüstite (Fe1-xO) is reviewed. The paper starts with a summary of applications where iron oxide surfaces play a major role, including corrosion, catalysis, spintronics, magnetic nanoparticles (MNPs), biomedicine, photoelectrochemical water splitting and groundwater remediation. The bulk structure and properties are then briefly presented; each compound is based on a close-packed anion lattice, with a different distribution and oxidation state of the Fe cations in interstitial sites. The bulk defect chemistry is dominated by cation vacancies and interstitials (not oxygen vacancies) and this provides the context to understand iron oxide surfaces, which represent the front line in reduction and oxidation processes. Fe diffuses in and out from the bulk in response to the O2 chemical potential, forming sometimes complex intermediate phases at the surface. For example, α-Fe2O3 adopts Fe3O4-like surfaces in reducing conditions, and Fe3O4 adopts Fe1-xO-like structures in further reducing conditions still. It is argued that known bulk defect structures are an excellent starting point in building models for iron oxide surfaces. The atomic-scale structure of the low-index surfaces of iron oxides is the major focus of this review. Fe3O4 is the most studied iron oxide in surface science, primarily because its stability range corresponds nicely to the ultra-high vacuum environment. It is also an electrical conductor, which makes it straightforward to study with the most commonly used surface science methods such as photoemission spectroscopies (XPS, UPS) and scanning tunneling microscopy (STM). The impact of the surfaces on the measurement of bulk properties such as magnetism, the Verwey transition and the (predicted) half-metallicity is discussed. The best understood iron oxide surface at present is probably Fe3O4(100); the structure is

  4. High temperature oxidation of iron-iron oxide core-shell nanowires composed of iron nanoparticles.

    Science.gov (United States)

    Krajewski, M; Brzozka, K; Lin, W S; Lin, H M; Tokarczyk, M; Borysiuk, J; Kowalski, G; Wasik, D

    2016-02-07

    This work describes an oxidation process of iron-iron oxide core-shell nanowires at temperatures between 100 °C and 800 °C. The studied nanomaterial was synthesized through a simple chemical reduction of iron trichloride in an external magnetic field under a constant flow of argon. The electron microscopy investigations allowed determining that the as-prepared nanowires were composed of self-assembled iron nanoparticles which were covered by a 3 nm thick oxide shell and separated from each other by a thin interface layer. Both these layers exhibited an amorphous or highly-disordered character which was traced by means of transmission electron microscopy and Mössbauer spectroscopy. The thermal oxidation was carried out under a constant flow of argon which contained the traces of oxygen. The first stage of process was related to slow transformations of amorphous Fe and amorphous iron oxides into crystalline phases and disappearance of interfaces between iron nanoparticles forming the studied nanomaterial (range: 25-300 °C). After that, the crystalline iron core and iron oxide shell became oxidized and signals for different compositions of iron oxide sheath were observed (range: 300-800 °C) using X-ray diffraction, Raman spectroscopy and Mössbauer spectroscopy. According to the thermal gravimetric analysis, the nanowires heated up to 800 °C under argon atmosphere gained 37% of mass with respect to their initial weight. The structure of the studied nanomaterial oxidized at 800 °C was mainly composed of α-Fe2O3 (∼ 93%). Moreover, iron nanowires treated above 600 °C lost their wire-like shape due to their shrinkage and collapse caused by the void coalescence.

  5. Accelerated dissolution of iron oxides in ice

    Directory of Open Access Journals (Sweden)

    D. Jeong

    2012-11-01

    Full Text Available Iron dissolution from mineral dusts and soil particles is vital as a source of bioavailable iron in various environmental media. In this work, the dissolution of iron oxide particles trapped in ice was investigated as a new pathway of iron supply. The dissolution experiments were carried out in the absence and presence of various organic complexing ligands under dark condition. In acidic pH conditions (pH 2, 3, and 4, the dissolution of iron oxides was greatly enhanced in the ice phase compared to that in water. The dissolved iron was mainly in the ferric form, which indicates that the dissolution is not a reductive process. The extent of dissolved iron was greatly affected by the kind of organic complexing ligands and the surface area of iron oxides. The iron dissolution was most pronounced with high surface area iron oxides and in the presence of strong iron binding ligands. The enhanced dissolution of iron oxides in ice is mainly ascribed to the "freeze concentration effect", which concentrates iron oxide particles, organic ligands, and protons in the liquid like ice grain boundary region and accelerates the dissolution of iron oxides. The ice-enhanced dissolution effect gradually decreased when decreasing the freezing temperature from −10 to −196 °C, which implies that the presence and formation of the liquid-like ice grain boundary region play a critical role. The proposed phenomenon of enhanced dissolution of iron oxides in ice may provide a new pathway of bioavailable iron production. The frozen atmospheric ice with iron-containing dust particles in the upper atmosphere thaws upon descending and may provide bioavailable iron upon deposition onto the ocean surface.

  6. Accelerated dissolution of iron oxides in ice

    Directory of Open Access Journals (Sweden)

    D. Jeong

    2012-08-01

    Full Text Available Iron dissolution from mineral dusts and soil particles is vital as a source of bioavailable iron in various environmental media. In this work, the dissolution of iron oxide particles trapped in ice was investigated as a~new pathway of iron supply. The dissolution experiments were carried out in the absence and presence of various organic complexing ligands under dark condition. In acidic pH conditions (pH 2, 3, and 4, the dissolution of iron oxides was greatly enhanced in the ice phase compared to that in water. The dissolved iron was mainly in the ferric form, which indicates that the dissolution is not a reductive process. The extent of dissolved iron was greatly affected by the kind of organic complexing ligands and the type of iron oxides. The iron dissolution was most pronounced with high surface area iron oxides and in the presence of strong iron binding ligands. The enhanced dissolution of iron oxides in ice is mainly ascribed to the "freeze concentration effect", which concentrates iron oxide particles, organic ligands, and protons in the liquid-like ice grain boundary region and accelerates the dissolution of iron oxides. The ice-enhanced dissolution effect gradually decreased when decreasing the freezing temperature from −10 °C to −196 °C, which implies that the presence and formation of the liquid-like ice grain boundary region play a critical role. The proposed phenomenon of enhanced dissolution of iron oxides in ice may provide a new pathway of bioavailable iron production. The frozen atmospheric ice with iron-containing dust particles in the upper atmosphere thaws upon descending and may provide bioavailable iron upon deposition onto the ocean surface.

  7. Iron, Oxidative Stress and Gestational Diabetes

    Directory of Open Access Journals (Sweden)

    Taifeng Zhuang

    2014-09-01

    Full Text Available Both iron deficiency and hyperglycemia are highly prevalent globally for pregnant women. Iron supplementation is recommended during pregnancy to control iron deficiency. The purposes of the review are to assess the oxidative effects of iron supplementation and the potential relationship between iron nutrition and gestational diabetes. High doses of iron (~relative to 60 mg or more daily for adult humans can induce lipid peroxidation in vitro and in animal studies. Pharmaceutical doses of iron supplements (e.g., 10× RDA or more for oral supplements or direct iron supplementation via injection or addition to the cell culture medium for a short or long duration will induce DNA damage. Higher heme-iron intake or iron status measured by various biomarkers, especially serum ferritin, might contribute to greater risk of gestational diabetes, which may be mediated by iron oxidative stress though lipid oxidation and/or DNA damage. However, information is lacking about the effect of low dose iron supplementation (≤60 mg daily on lipid peroxidation, DNA damage and gestational diabetes. Randomized trials of low-dose iron supplementation (≤60 mg daily for pregnant women are warranted to test the relationship between iron oxidative stress and insulin resistance/gestational diabetes, especially for iron-replete women.

  8. Dextran-modified iron oxide nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Ji(r)í Hradil; Alexander Pisarev; Michal Babi(c); Daniel Horák

    2007-01-01

    Dextran-modified iron oxide nanoparticles were prepared by precipitation of Fe(Ⅱ) and Fe(Ⅲ) salts with ammonium hydroxide by two methods.Iron oxide was precipitated either in the presence of dextran solution, or the dextran solution was added after precipitation. In the second method,the iron oxide particle size and size distribution could be controlled depending on the concentration of dextran in the solution. The nanoparticles were characterized by size-exclusion chromatography, transmission electron microscopy and dynamic light scattering. Optimal conditions for preparation of stable iron oxide colloid particles were determined. The dextran/iron oxide ratio 0-0.16 used in precipitation of iron salts can be recommended for synthesis of nanoparticles suitable for biomedical applications, as the colloid does not contain excess dextran and does not coagulate.

  9. Core-shell iron-iron oxide nanoparticles

    DEFF Research Database (Denmark)

    Kuhn, Luise Theil; Bojesen, A.; Timmermann, L.

    2004-01-01

    We present studies of the magnetic properties of core-shell iron-iron oxide nanoparticles. By combining Mossbauer and X-ray absorption spectroscopy we have been able to measure the change from a Fe3O4-like to a gamma-Fe2O3-like composition from the interface to the surface. Furthermore, we have...

  10. Tannin biosynthesis of iron oxide nanoparticles

    Science.gov (United States)

    Herrera-Becerra, R.; Rius, J. L.; Zorrilla, C.

    2010-08-01

    In this work, iron oxide nanoparticles synthesized with gallic acid and tannic acid are characterized using High-Resolution Transmission Electron Microscopy (HRTEM). Its size, form, and structure are compared with nanoparticles obtained previously using alfalfa biomass in order to find a simpler, consistent, and environmentally friendly method in the production of iron oxide nanoparticles.

  11. Analysis of iron oxidation at high temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Slattery, J.C.; Peng, K.Y.; Gadalla, A.M.; Gadalla, N. [Texas A and M Univ., College Station, TX (United States). Dept. of Chemical Engineering

    1995-10-01

    A new theory for the high-temperature oxidation of iron is proposed, in which the rate-limiting step is ternary diffusion of ferric, ferrous, and oxygen ions in the iron oxides that are formed. The predictions of this theory are compared with previously published experimental data. The only thermodynamic information required is a phase diagram.

  12. Carbon-Supported Iron Oxide Particles

    DEFF Research Database (Denmark)

    Meaz, T.; Mørup, Steen; Koch, C. Bender

    1996-01-01

    A carbon black ws impregnated with 6 wt% iron using an aqueous solution of iron nitrate. The impregnated carbon was initially dried at 125 C. The effect of heating of the iron oxide phase was investigated at temperatures between 200 and 600 C using Mossbauer spectroscopy. All heat treatments were...... done in an oxygen-containing atmosphere. Ferrihydrite is formed and is stable at and below a temperature of 300 C. At 600 C small particles of maghemite is the dominant iron oxide. A transformation reaction is suggested....

  13. On the formation of iron(III) oxides via oxidation of iron(II)

    Energy Technology Data Exchange (ETDEWEB)

    Bongiovanni, R.; Pelizzetti, E. [Torino Univ. (Italy). Dipt. di Chimica Analitica; Borgarello, E. [Eniricerche SpA, Milan (Italy); Meisel, D. [Argonne National Lab., IL (United States)

    1994-09-01

    Formation of iron oxides in aqueous salt solutions is reviewed. The discussion is focused on the oxidation of iron(II) and the following hydrolysis process that leads to the formation of a solid phase from homogeneous solutions. Results from our own studies on the kinetics of the oxidation reactions and the ensuing growth processes are presented.

  14. EXPLORING MICROBIAL IRON OXIDATION IN WETLAND SOILS

    NARCIS (Netherlands)

    Wang, J.; Den Oudsten, F.; Meima-Franke, M.; Vollrath, S.; Muyzer, G.; Bodelier, P.L.E.; Laanbroek, H.J.

    2010-01-01

    The release of oxygen by the roots of wetland plants creates suboxic conditions that may favour the growth of iron-oxidizing bacteria (FeOB). Given their importance in iron cycling, little is known about the diversity or distribution of these bacteria. This is largely due to the lack of efficient me

  15. Sophorolipids-functionalized iron oxide nanoparticles

    OpenAIRE

    Baccile, Niki; Noiville, Romain; Stievano, Lorenzo; Van Bogaert, Inge

    2013-01-01

    International audience; Functional iron oxide nanoparticles (NP) have been synthesized in a one and a two-step method using a natural functional glycolipid belonging to the family of sophorolipids (SL). These compounds, whose open acidic form is highly suitable for nanoparticle stabilization, are readily obtained by a fermentation process of the yeast Candida bombicola (polymorph Starmerella bombicola) in large amounts. The final carbohydrate coated iron oxide nanoparticles represent interest...

  16. The irony of iron -- biogenic iron oxides as an iron source to the ocean

    Directory of Open Access Journals (Sweden)

    David eEmerson

    2016-01-01

    Full Text Available Primary productivity in at least a third of the sunlit open ocean is thought to be iron-limited. Primary sources of dissolved iron (dFe to the ocean are hydrothermal venting, flux from the sediments along continental margins, and airborne dust. This article provides a general review of sources of hydrothermal and sedimentary iron to the ocean, and speculates upon the role that iron-cycling microbes play in controlling iron dynamics from these sources. Special attention is paid to iron-oxidizing bacteria (FeOB that live by oxidizing iron and producing biogenic iron oxides as waste products. The presence and ubiquity of FeOB both at hydrothermal systems and in sediments is only beginning to be appreciated. The biogenic oxides they produce have unique properties that could contribute significantly to the dynamics of dFe in the ocean. Changes in the physical and chemical characteristics of the ocean due to climate change and ocean acidification will undoubtedly impact the microbial iron cycle. A better understanding of the contemporary role of microbes in the iron cycle will help in predicting how these changes could ultimately influence marine primary productivity.

  17. Water clustering on nanostructured iron oxide films

    DEFF Research Database (Denmark)

    Merte, Lindsay Richard; Bechstein, Ralf; Peng, G.;

    2014-01-01

    , but it is not well-understood how these hydroxyl groups and their distribution on a surface affect the molecular-scale structure at the interface. Here we report a study of water clustering on a moire-structured iron oxide thin film with a controlled density of hydroxyl groups. While large amorphous monolayer...... islands form on the bare film, the hydroxylated iron oxide film acts as a hydrophilic nanotemplate, causing the formation of a regular array of ice-like hexameric nanoclusters. The formation of this ordered phase is localized at the nanometre scale; with increasing water coverage, ordered and amorphous...

  18. Relationship Between Iron Oxides and Surface Charge Characteristics in Soils

    Institute of Scientific and Technical Information of China (English)

    SHAOZONG-CHEN; WANGWEI-JUN

    1991-01-01

    The relationship between iron oxides and surface charge characteristics in variable charge soils (latosol and red earth) was studied in following three ways.(1)Remove free iron oxides (Fed) and amorphous iron oxides (Feo) from the soils with sodium dithionite and acid ammonium oxalate solution respectively.(2) Add 2% glucose (on the basis of air-dry soil weight) to soils and incubate under submerged condition to activate iron oxides,and then the mixtures are dehydrated and air-dried to age iron oxides.(3) Precipitate various crystalline forms of iron oxides onto kaolinite.The results showed that free iron oxides (Fed) were the chief carrier of variable positive charges.Of which crystalline iron oxides (Fed-Feo) presented mainly as discrete particles in the soils and could only play a role of the carrier of positive charges,and did little influence on negative charges.Whereas the amorphous iron oxides (Feo),which presented mainly fas a coating with a large specific surface area,not only had positive charges,but also blocked the negative charge sites in soils.Submerged incubation activated iron oxides in the soils,and increased the amount of amorphous iron oxides and the degree of activation of iron oxide,which resulted in the increase of positive and negative charges of soils.Dehydration and air-dry aged iron oxides in soils and decreased the amount of amorphous iron oxides and the degree of activation of iron oxide,and also led to the decrease of positive and negative charges.Both the submerged incubation and the dehydration and air-dry had no significant influence on net charges.Precipitation of iron oxides onto kaolinite markedly increased positive charges and decreased negative charges.Amorphous iron oxide having a larger surface area contributed more positive charge sites and blocked more negative charge sites in kaolinite than crystalline goethite.

  19. Iron oxides in human spleen.

    Science.gov (United States)

    Kopáni, Martin; Miglierini, Marcel; Lančok, Adriana; Dekan, Július; Čaplovicová, Mária; Jakubovský, Ján; Boča, Roman; Mrazova, Hedviga

    2015-10-01

    Iron is an essential element for fundamental cell functions and a catalyst for chemical reactions. Three samples extracted from the human spleen were investigated by scanning (SEM) and transmission electron microscopy (TEM), Mössbauer spectrometry (MS), and SQUID magnetometry. The sample with diagnosis of hemosiderosis (H) differs from that referring to hereditary spherocytosis and the reference sample. SEM reveals iron-rich micrometer-sized aggregate of various structures-tiny fibrils in hereditary spherocytosis sample and no fibrils in hemochromatosis. Hematite and magnetite particles from 2 to 6 μm in TEM with diffraction in all samples were shown. The SQUID magnetometry shows different amount of diamagnetic, paramagnetic and ferrimagnetic structures in the tissues. The MS results indicate contribution of ferromagnetically split sextets for all investigated samples. Their occurrence indicates that at least part of the sample is magnetically ordered below the critical temperature. The iron accumulation process is different in hereditary spherocytosis and hemosiderosis. This fact may be the reason of different iron crystallization.

  20. Iron-iron oxide core-shell nanoparticles synthesized by laser pyrolysis followed by superficial oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Dumitrache, F. [National Institute for Lasers, Plasma and Radiation Physics, P.O. Box MG-36, 077125 Bucharest (Romania)]. E-mail: fdumit@inflpr.ro; Morjan, I. [National Institute for Lasers, Plasma and Radiation Physics, P.O. Box MG-36, 077125 Bucharest (Romania); Alexandrescu, R. [National Institute for Lasers, Plasma and Radiation Physics, P.O. Box MG-36, 077125 Bucharest (Romania); Ciupina, V. [' Ovidius' University of Constanta, Bd. Mamaia 124, Constanta (Romania); Prodan, G. [' Ovidius' University of Constanta, Bd. Mamaia 124, Constanta (Romania); Voicu, I. [National Institute for Lasers, Plasma and Radiation Physics, P.O. Box MG-36, 077125 Bucharest (Romania); Fleaca, C. [National Institute for Lasers, Plasma and Radiation Physics, P.O. Box MG-36, 077125 Bucharest (Romania); Albu, L. [National Institute for Lasers, Plasma and Radiation Physics, P.O. Box MG-36, 077125 Bucharest (Romania); Savoiu, M. [National Institute for Lasers, Plasma and Radiation Physics, P.O. Box MG-36, 077125 Bucharest (Romania); Sandu, I. [National Institute for Lasers, Plasma and Radiation Physics, P.O. Box MG-36, 077125 Bucharest (Romania); Popovici, E. [National Institute for Lasers, Plasma and Radiation Physics, P.O. Box MG-36, 077125 Bucharest (Romania); Soare, I. [National Institute for Lasers, Plasma and Radiation Physics, P.O. Box MG-36, 077125 Bucharest (Romania)

    2005-07-15

    Iron-based core-shell nanostructures were synthesized by laser pyrolysis in a two-steps procedure. In a first step, using a cross-flow configuration, the laser radiation was heating a gas phase mixture containing iron pentacarbonyl (vapors) entrained by an ethylene flow, which plays also the role of an energy transfer agent. Secondly, a carefully controlled in situ passivation of the freshly formed pyrophoric iron nanoparticles created a protective iron oxide shell. The produced nanoparticles (22 nm size diameters) with core-shell features were analyzed by TEM, XRD, SAED and Raman spectroscopy. Majoritary iron and gamma iron oxide/magnetite and minoritary carbon phases were identified. In laser pyrolysis experiments in which the reaction temperature was increased, the catalyzed homogeneous nucleation and growth of carbon nanotubes in the gas phase was observed and is presented here for the first time.

  1. Iron iron oxide core shell nanoparticles synthesized by laser pyrolysis followed by superficial oxidation

    Science.gov (United States)

    Dumitrache, F.; Morjan, I.; Alexandrescu, R.; Ciupina, V.; Prodan, G.; Voicu, I.; Fleaca, C.; Albu, L.; Savoiu, M.; Sandu, I.; Popovici, E.; Soare, I.

    2005-07-01

    Iron-based core-shell nanostructures were synthesized by laser pyrolysis in a two-steps procedure. In a first step, using a cross-flow configuration, the laser radiation was heating a gas phase mixture containing iron pentacarbonyl (vapors) entrained by an ethylene flow, which plays also the role of an energy transfer agent. Secondly, a carefully controlled in situ passivation of the freshly formed pyrophoric iron nanoparticles created a protective iron oxide shell. The produced nanoparticles (22 nm size diameters) with core-shell features were analyzed by TEM, XRD, SAED and Raman spectroscopy. Majoritary iron and gamma iron oxide/magnetite and minoritary carbon phases were identified. In laser pyrolysis experiments in which the reaction temperature was increased, the catalyzed homogeneous nucleation and growth of carbon nanotubes in the gas phase was observed and is presented here for the first time.

  2. Defluoridation by Bacteriogenic Iron Oxides: Sorption Studies

    Science.gov (United States)

    Evans, K.; Ferris, F.

    2009-05-01

    At concentrations above 1 mg/L, fluoride in drinking water can lead to dental and skeletal fluorosis, a disease that causes mottling of the teeth, calcification of ligaments, crippling bone deformities and many other physiological disorders that can, ultimately, lead to death. Conservative estimates are that fluorosis afflicts tens of millions of people worldwide. As there is no treatment for fluorosis, prevention is the only means of controlling the disease. While numerous defluoridation techniques have been explored, no single method has been found to be both effective and inexpensive enough to implement widely. Our research began in India, with a large-scale geochemical study of the groundwater in a fluoride-contaminated region of Orissa. Having developed a better understanding of the geochemical relationships that exist between fluoride and other parameters present in an affected area, as well as the complex relationships that arise among those parameters that can impact the presence of fluoride, we began investigating certain remediation scenarios involving iron oxides. A common approach to remediation involves the partitioning of fluoride from groundwater by sorption onto a variety of materials, one of the most effective of which is iron oxide whose surface area acts as a scavenger for fluoride. In the presence of iron oxidizing bacteria, the oxidation rate of iron has been shown to be ˜6 times greater than in their absence; fluoride should, therefore, be removed from an aqueous environment by bacteriogenic iron oxides (BIOS) much more quickly than by abiotic iron oxides. Most recently, sorption studies have been conducted using both BIOS and synthetic hydrous ferric oxides in order to compare the behavior between biotic and abiotic sorbents. These studies have provided sorption isotherms that allow comparison of fluoride removed by sorption to BIOS versus synthetic iron oxides. Sorption affinity constants have also been determined, which allow for the

  3. Mixed iron-manganese oxide nanoparticles

    NARCIS (Netherlands)

    Lai, Jriuan; Shafi, Kurikka V.P.M.; Ulman, Abraham; Loos, Katja; Yang, Nan-Loh; Cui, Min-Hui; Vogt, Thomas; Estournès, Claude; Locke, Dave C.

    2004-01-01

    Designing nanoparticles for practical applications requires knowledge and control of how their desired properties relate to their composition and structure. Here, we present a detailed systematic study of mixed iron-manganese oxide nanoparticles, showing that ultrasonication provides the high-energy

  4. Chemical design of biocompatible iron oxide nanoparticles for medical applications.

    Science.gov (United States)

    Ling, Daishun; Hyeon, Taeghwan

    2013-05-27

    Iron oxide nanoparticles are one of the most versatile and safe nanomaterials used in medicine. Recent progress in nanochemistry enables fine control of the size, crystallinity, uniformity, and surface properties of iron oxide nanoparticles. In this review, the synthesis of chemically designed biocompatible iron oxide nanoparticles with improved quality and reduced toxicity is discussed for use in diverse biomedical applications.

  5. Acid monolayer functionalized iron oxide nanoparticle catalysts

    Science.gov (United States)

    Ikenberry, Myles

    Superparamagnetic iron oxide nanoparticle functionalization is an area of intensely active research, with applications across disciplines such as biomedical science and heterogeneous catalysis. This work demonstrates the functionalization of iron oxide nanoparticles with a quasi-monolayer of 11-sulfoundecanoic acid, 10-phosphono-1-decanesulfonic acid, and 11-aminoundecanoic acid. The carboxylic and phosphonic moieties form bonds to the iron oxide particle core, while the sulfonic acid groups face outward where they are available for catalysis. The particles were characterized by thermogravimetric analysis (TGA), transmission electron microscopy (TEM), potentiometric titration, diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), inductively coupled plasma optical emission spectrometry (ICP-OES), X-ray photoelectron spectrometry (XPS), and dynamic light scattering (DLS). The sulfonic acid functionalized particles were used to catalyze the hydrolysis of sucrose at 80° and starch at 130°, showing a higher activity per acid site than the traditional solid acid catalyst Amberlyst-15, and comparing well against results reported in the literature for sulfonic acid functionalized mesoporous silicas. In sucrose catalysis reactions, the phosphonic-sulfonic nanoparticles (PSNPs) were seen to be incompletely recovered by an external magnetic field, while the carboxylic-sulfonic nanoparticles (CSNPs) showed a trend of increasing activity over the first four recycle runs. Between the two sulfonic ligands, the phosphonates produced a more tightly packed monolayer, which corresponded to a higher sulfonic acid loading, lower agglomeration, lower recoverability through application of an external magnetic field, and higher activity per acid site for the hydrolysis of starch. Functionalizations with 11-aminoundecanoic acid resulted in some amine groups binding to the surfaces of iron oxide nanoparticles. This amine binding is commonly ignored in iron oxide

  6. Physicochemical nature of iron oxidation in a damp atmospheric condition

    Institute of Scientific and Technical Information of China (English)

    Tongyan PAN; Yunpinq XI

    2011-01-01

    The surface oxidation patterns of iron or low-carbon steels are critical to their life when serving in typical damp environments.An accurate determination of the oxidation pattern entails tracking the iron atoms oxidized at the iron/steel-moisture interface.Using a quantum chemistry-based force field that is capable of simulating chemical reactions,this paper studies the process of iron oxidation under a typical moist condition. The oxidation of iron surface was found to be highly thermodynamic and dependent on the availability of reactants.A triplex structure was formed at the end of a three-stage oxidation process to reduce the overall oxidation speed.The results from this study shed light on the atomistic mechanism of iron oxidation; therefore can be used to guide the protection of general ferrous-based iron/steel structures.

  7. Nitric oxide and plant iron homeostasis.

    Science.gov (United States)

    Buet, Agustina; Simontacchi, Marcela

    2015-03-01

    Like all living organisms, plants demand iron (Fe) for important biochemical and metabolic processes. Internal imbalances, as a consequence of insufficient or excess Fe in the environment, lead to growth restriction and affect crop yield. Knowledge of signals and factors affecting each step in Fe uptake from the soil and distribution (long-distance transport, remobilization from old to young leaves, and storage in seeds) is necessary to improve our understanding of plant mineral nutrition. In this context, the role of nitric oxide (NO) is discussed as a key player in maintaining Fe homeostasis through its cross talk with hormones, ferritin, and frataxin and the ability to form nitrosyl-iron complexes.

  8. Oxidation of Dodecanoate Intercalated Iron(II)–Iron(III) Layered Double Hydroxide to Form 2D Iron(III) (Hydr)oxide Layers

    DEFF Research Database (Denmark)

    Huang, Li‐Zhi; Ayala‐Luis, Karina B.; Fang, Liping;

    2013-01-01

    A planar trioctahedral iron(II)–iron(III) hydroxide (green rust, GR) intercalated with dodecanoate (GRC12) has been oxidized by dioxygen to produce the corresponding planar iron(III) (hydr)oxide. The formulae of GRC12 and the final iron(III) product (oxGRC12) were determined to be FeII2.00FeIII1...

  9. Oxidation Potentials in Iron and Steel Making

    Science.gov (United States)

    Matousek, J. W.

    2013-11-01

    The state of oxidation of a pyrometallurgical process given by the partial pressure of oxygen and the temperature (the oxidation potential) is one of the important properties monitored and controlled in the smelting and refining of iron and the nonferrous metals. Solid electrolyte sensors based on ZrO2 and a reference electrode such as Cr/Cr2O3 to measure the oxygen pressure found early application in the steel industry, followed soon after in copper, nickel, lead, and zinc smelting. Similar devices are installed in automobile postcombustion/exhaust trains as part of emission control systems. The current discussion reviews this technology as applied in the primary steps of iron and steel making and refining.

  10. Scalable Production of Iron Oxide Nanowhiskers

    Directory of Open Access Journals (Sweden)

    Thomas Macher

    2015-01-01

    Full Text Available We reported the scalable production of iron oxide nanowhiskers from 250 mL laboratory scale to 10 L reactor reaction. During the scale-up process, the reaction time was found to be a critical parameter to adjust for the production of iron oxide nanowhiskers with similar quality to that of the laboratory scale. Based on transmission electron microscopy and magnetometry analysis, the size, size distribution, and magnetic properties of the large scale products were comparable to those produced on laboratory scale. Subsequently, these nanowhiskers were transferred from organic solvents to aqueous solution using a 38-liter stainless steel tank. These water soluble nanowhiskers were well dispersed in water and the surface chemistry was confirmed by Fourier transform infrared spectroscopy.

  11. Ferrite grade iron oxides from ore rejects

    Indian Academy of Sciences (India)

    K S Rane; V M S Verenkar; P Y Sawant

    2001-06-01

    Iron oxyhydroxides and hydroxides were synthesized from chemically beneficiated high SiO2/Al2O3 low-grade iron ore (57.49% Fe2O3) rejects and heated to get iron oxides of 96–99.73% purity. The infrared band positions, isothermal weight loss and thermogravimetric and chemical analysis established the chemical formulas of iron-oxyhydroxides as -FeOOH.0.3H2O; -FeOOH.0.2H2O and amorphous FeOOH. The thermal products of all these were -Fe2O3 excepting that of -FeOOH.0.3H2O which gave mainly -Fe2O3 and some admixture of -Fe2O3. The hydrazinated iron hydroxides and oxyhydroxides, on the other hand, decomposed autocatalytically to mainly -Fe2O3. Hydrazine method modifies the thermal decomposition path of the hydroxides. The saturation magnetization, s, values were found to be in the range 60–71 emu g–1 which are close to the reported values for -Fe2O3. Mechanism of the -Fe2O3 formation by hydrazine method is discussed.

  12. Effects of coating spherical iron oxide nanoparticles

    OpenAIRE

    2016-01-01

    International audience; We investigate the effect of several coatings applied in biomedical applications to iron oxide nanoparticles on the size, structure and composition of the particles. The four structural techniques employed – TEM, DLS, VSM, SAXS and EXAFS – show no significant effects of the coatings on the spherical shape of the bare nanoparticles, the average sizes or the local order around the Fe atoms. The NPs coated with hydroxylmethylene bisphosphonate or catechol have a lower pro...

  13. Nitrate-dependent iron oxidation limits iron transport in anoxic ocean regions

    DEFF Research Database (Denmark)

    Scholz, Florian; Löscher, Carolin; Fiskal, Annika;

    2016-01-01

    campaign the water column featured two distinct redox boundaries separating oxic from nitrate-reducing (i.e., nitrogenous) water and nitrogenous from weakly sulfidic water. The sulfidic water mass in contact with the shelf sediment contained elevated iron concentrations>300 nM. At the boundary between...... sulfidic and nitrogenous conditions, iron concentrations dropped sharply to ... to the activity of known iron-oxidizing bacteria. Collectively, our data suggest that iron oxidation and removal is induced by nitrate-reducing microbes, either enzymatically through anaerobic iron oxidation or by providing nitrite for an abiotic reaction. Given the important role that iron plays in nitrogen...

  14. Methyltrimethoxysilane (MTMS)-based silica-iron oxide superhydrophobic nanocomposites.

    Science.gov (United States)

    Nadargi, Digambar; Gurav, Jyoti; Marioni, Miguel A; Romer, Sara; Matam, Santhosh; Koebel, Matthias M

    2015-12-01

    We report a facile synthesis of superhydrophobic silica-iron oxide nanocomposites via a co-precursor sol-gel process. The choice of the silica precursor (Methyltrimethoxysilane, MTMS) in combination with iron nitrate altered the pore structure dramatically. The influence of iron oxide doping on the structural properties of pristine MTMS aerogel is discussed.

  15. Water Clustering on Nanostructured Iron Oxide Films

    Energy Technology Data Exchange (ETDEWEB)

    Merte, L. R.; Bechstein, Ralf; Peng, Guowen; Rieboldt, Felix; Farberow, Carrie A.; Zeuthen, Helene; Knudsen, Jan; Laegsgaard, E.; Wendt, Stefen; Mavrikakis, Manos; Besenbacher, Fleming

    2014-06-30

    The adhesion of water to solid surfaces is characterized by the tendency to balance competing molecule–molecule and molecule–surface interactions. Hydroxyl groups form strong hydrogen bonds to water molecules and are known to substantially influence the wetting behaviour of oxide surfaces, but it is not well-understood how these hydroxyl groups and their distribution on a surface affect the molecular-scale structure at the interface. Here we report a study of water clustering on a moire´-structured iron oxide thin film with a controlled density of hydroxyl groups. While large amorphous monolayer islands form on the are film, the hydroxylated iron oxide film acts as a hydrophilic nanotemplate, causing the formation of a regular array of ice-like hexameric nanoclusters. The formation of this ordered phase is localized at the nanometre scale; with increasing water coverage, ordered and amorphous water are found to coexist at adjacent hydroxylated and hydroxyl-free domains of the moire´ structure.

  16. Phase Formation Behavior in Ultrathin Iron Oxide.

    Science.gov (United States)

    Jõgi, Indrek; Jacobsson, T Jesper; Fondell, Mattis; Wätjen, Timo; Carlsson, Jan-Otto; Boman, Mats; Edvinsson, Tomas

    2015-11-17

    Nanostructured iron oxides, and especially hematite, are interesting for a wide range of applications ranging from gas sensors to renewable solar hydrogen production. A promising method for deposition of low-dimensional films is atomic layer deposition (ALD). Although a potent technique, ALD of ultrathin films is critically sensitive to the substrate and temperature conditions where initial formation of islands and crystallites influences the properties of the films. In this work, deposition at the border of the ALD window forming a hybrid ALD/pulsed CVD (pCVD) deposition is utilized to obtain a deposition less sensitive to the substrate. A thorough analysis of iron oxide phases formation on two different substrates, Si(100) and SiO2, was performed. Films between 3 and 50 nm were deposited and analyzed with diffraction techniques, high-resolution Raman spectroscopy, and optical spectroscopy. Below 10 nm nominal film thickness, island formation and phase dependent particle crystallization impose constraints for deposition of phase pure iron oxides on non-lattice-matching substrates. Films between 10 and 20 nm thickness on SiO2 could effectively be recrystallized into hematite whereas for the corresponding films on Si(100), no recrystallization occurred. For films thicker than 20 nm, phase pure hematite can be formed directly with ALD/pCVD with very low influence of the substrate on either Si or SiO2. For more lattice matched substrates such as SnO2:F, Raman spectroscopy indicated formation of the hematite phase already for films with 3 nm nominal thickness and clearly for 6 nm films. Analysis of the optical properties corroborated the analysis and showed a quantum confined blue-shift of the absorption edge for the thinnest films.

  17. The Sulfide Capacity of Iron Oxide-Rich Slags

    Science.gov (United States)

    Motlagh, M.

    1988-03-01

    The relationship between the sulfide capacity of slags rich in iron oxide and the sulfur partition ratio between the metal and slag is strongly related to the slag's iron oxide concentration. For slags containing little or no lime, this relationship is linear for a constant concentration of iron oxide in the slag. The effect of silica on changes in the sulfide capacity of slags rich in iron oxide is similar to that of basic steel-making slags, particularly at low activity of silica in slag.

  18. Suspension Hydrogen Reduction of Iron Oxide Concentrates

    Energy Technology Data Exchange (ETDEWEB)

    H.Y. Sohn

    2008-03-31

    The objective of the project is to develop a new ironmaking technology based on hydrogen and fine iron oxide concentrates in a suspension reduction process. The ultimate objective of the new technology is to replace the blast furnace and to drastically reduce CO2 emissions in the steel industry. The goals of this phase of development are; the performance of detailed material and energy balances, thermochemical and equilibrium calculations for sulfur and phosphorus impurities, the determination of the complete kinetics of hydrogen reduction and bench-scale testing of the suspension reduction process using a large laboratory flash reactor.

  19. Modified iron oxide nanomaterials: Functionalization and application

    Science.gov (United States)

    Bagheri, Samira; Julkapli, Nurhidayatullaili Muhd

    2016-10-01

    Iron oxide magnetic nanoparticles have aroused the interest of researchers of materials' chemistry due to its exceptional properties such as decent magnetic, electric, catalytic, biocompatibility, and low toxicity. However, these magnetic nanoparticles are predisposed towards aggregation and forming larger particles, due to its strong anisotropic dipolar interactions, particularly in the aqueous phase, consequently depriving them of dispersibility and particular properties, ultimately degrading their performance. Hence, this review focuses on modified magnetic nanoparticles that are stable, easily synthesized, possess a high surface area and could be facile-separated via magnetic forces, and are of low toxicity and costs for applications such as catalyst/catalyst support, food security, biomedical, and pollutant remediation.

  20. Nitrate-dependent iron oxidation limits iron transport in anoxic ocean regions

    Science.gov (United States)

    Scholz, Florian; Löscher, Carolin R.; Fiskal, Annika; Sommer, Stefan; Hensen, Christian; Lomnitz, Ulrike; Wuttig, Kathrin; Göttlicher, Jörg; Kossel, Elke; Steininger, Ralph; Canfield, Donald E.

    2016-11-01

    Iron is an essential element for life on Earth and limits primary production in large parts of the ocean. Oxygen-free continental margin sediments represent an important source of bioavailable iron to the ocean, yet little of the iron released from the seabed reaches the productive sea surface. Even in the anoxic water of oxygen minimum zones, where iron solubility should be enhanced, most of the iron is rapidly re-precipitated. To constrain the mechanism(s) of iron removal in anoxic ocean regions we explored the sediment and water in the oxygen minimum zone off Peru. During our sampling campaign the water column featured two distinct redox boundaries separating oxic from nitrate-reducing (i.e., nitrogenous) water and nitrogenous from weakly sulfidic water. The sulfidic water mass in contact with the shelf sediment contained elevated iron concentrations >300 nM. At the boundary between sulfidic and nitrogenous conditions, iron concentrations dropped sharply to nitrate reduction (narG). Part of this upregulation was related to the activity of known iron-oxidizing bacteria. Collectively, our data suggest that iron oxidation and removal is induced by nitrate-reducing microbes, either enzymatically through anaerobic iron oxidation or by providing nitrite for an abiotic reaction. Given the important role that iron plays in nitrogen fixation, photosynthesis and respiration, nitrate-dependent iron oxidation likely represents a key-link between the marine biogeochemical cycles of nitrogen, oxygen and carbon.

  1. Toxicity of iron oxide nanoparticles against osteoblasts

    Energy Technology Data Exchange (ETDEWEB)

    Shi Sifeng [Shanghai Jiao Tong University, Department of Orthopaedic Surgery, Shanghai Sixth People' s Hospital (China); Jia Jingfu [Shanghai Jiao Tong University, School of Chemistry and Chemical Technology (China); Guo Xiaokui [Shanghai Jiao Tong University School of Medicine, Department of Medical Microbiology and Parasitology, Institutes of Medical Sciences (China); Zhao Yaping [Shanghai Jiao Tong University, School of Chemistry and Chemical Technology (China); Liu Boyu [Shanghai Jiao Tong University School of Medicine, Department of Medical Microbiology and Parasitology, Institutes of Medical Sciences (China); Chen Desheng; Guo Yongyuan; Zhang Xianlong, E-mail: zhangxianlong20101@163.com [Shanghai Jiao Tong University, Department of Orthopaedic Surgery, Shanghai Sixth People' s Hospital (China)

    2012-09-15

    Magnetic nanoparticles have been widely used for tissue repair, magnetic resonance imaging, immunoassays and drug delivery. They are very promising in orthopaedic applications and several magnetic nanoparticles have been exploited for the treatment of orthopaedic disease. Here, we conducted an in vitro study to examine the interaction of magnetic iron oxide nanoparticles with human osteoblasts to evaluate the dose-related toxicity of the nanoparticles on osteoblasts. A transmission electron microscope was used to visualise the internalised magnetic nanoparticles in osteoblasts. The CCK-8 results revealed increased cell viability (107.5 % vitality compared with the control group) when co-cultured at a low concentration (20 {mu}g/mL) and decreased cell viability (59.5 % vitality in a concentration of 300 {mu}g/mL and 25.9 % in 500 {mu}g/mL) when co-cultured in high concentrations. The flow cytometric detection revealed similar results with 5.48 % of apoptosis in a concentration of 20 {mu}g/mL, 23.40 % of apoptosis in a concentration of 300 {mu}g/mL and 28.49 % in a concentration of 500 {mu}g/mL. The disrupted cytoskeleton of osteoblasts was also revealed using a laser scanning confocal microscope. We concluded that use of a low concentration of magnetic iron oxide nanoparticles is important to avoid damage to osteoblasts.

  2. Bismuth iron oxide thin films using atomic layer deposition of alternating bismuth oxide and iron oxide layers

    Energy Technology Data Exchange (ETDEWEB)

    Puttaswamy, Manjunath; Vehkamäki, Marko [University of Helsinki, Department of Chemistry, P.O. Box 55, FI-00014 Helsinki (Finland); Kukli, Kaupo, E-mail: kaupo.kukli@helsinki.fi [University of Helsinki, Department of Chemistry, P.O. Box 55, FI-00014 Helsinki (Finland); University of Tartu, Institute of Physics, W. Ostwald 1, EE-50411 Tartu (Estonia); Dimri, Mukesh Chandra [National Institute of Chemical Physics and Biophysics, Akadeemia tee 23, EE-12618 Tallinn (Estonia); Kemell, Marianna; Hatanpää, Timo; Heikkilä, Mikko J. [University of Helsinki, Department of Chemistry, P.O. Box 55, FI-00014 Helsinki (Finland); Mizohata, Kenichiro [University of Helsinki, Department of Physics, P.O. Box 64, FI-00014 Helsinki (Finland); Stern, Raivo [National Institute of Chemical Physics and Biophysics, Akadeemia tee 23, EE-12618 Tallinn (Estonia); Ritala, Mikko; Leskelä, Markku [University of Helsinki, Department of Chemistry, P.O. Box 55, FI-00014 Helsinki (Finland)

    2016-07-29

    Bismuth iron oxide films with varying contributions from Fe{sub 2}O{sub 3} or Bi{sub 2}O{sub 3} were prepared using atomic layer deposition. Bismuth (III) 2,3-dimethyl-2-butoxide, was used as the bismuth source, iron(III) tert-butoxide as the iron source and water vapor as the oxygen source. The films were deposited as stacks of alternate Bi{sub 2}O{sub 3} and Fe{sub 2}O{sub 3} layers. Films grown at 140 °C to the thickness of 200–220 nm were amorphous, but crystallized upon post-deposition annealing at 500 °C in nitrogen. Annealing of films with intermittent bismuth and iron oxide layers grown to different thicknesses influenced their surface morphology, crystal structure, composition, electrical and magnetic properties. Implications of multiferroic performance were recognized in the films with the remanent charge polarization varying from 1 to 5 μC/cm{sup 2} and magnetic coercivity varying from a few up to 8000 A/m. - Highlights: • Bismuth iron oxide thin films were grown by atomic layer deposition at 140 °C. • The major phase formed in the films upon annealing at 500 °C was BiFeO{sub 3}. • BiFeO{sub 3} films and films containing excess Bi favored electrical charge polarization. • Slight excess of iron oxide enhanced saturative magnetization behavior.

  3. Structural and magnetic properties of core-shell iron-iron oxide nanoparticles

    DEFF Research Database (Denmark)

    Kuhn, Luise Theil; Bojesen, A.; Timmermann, L.

    2002-01-01

    We present studies of the structural and magnetic properties of core-shell iron-iron oxide nanoparticles. alpha-Fe nanoparticles were fabricated by sputtering and subsequently covered with a protective nanocrystalline oxide shell consisting of either maghaemite (gamma-Fe2O3) or partially oxidized...... magnetite (Fe3O4). We observed that the nanoparticles were stable against further oxidation, and Mossbauer spectroscopy at high applied magnetic fields and low temperatures revealed a stable form of partly oxidized magnetite. The nanocrystalline structure of the oxide shell results in strong canting...... of the spin structure in the oxide shell, which thereby modifies the magnetic properties of the core-shell nanoparticles....

  4. Bio-inspired Iron Catalysts for Hydrocarbon Oxidations

    Energy Technology Data Exchange (ETDEWEB)

    Que, Jr., Lawrence [Univ. of Minnesota, Minneapolis, MN (United States)

    2016-03-22

    Stereoselective oxidation of C–H and C=C bonds are catalyzed by nonheme iron enzymes. Inspired by these bioinorganic systems, our group has been exploring the use of nonheme iron complexes as catalysts for the oxidation of hydrocarbons using H2O2 as an environmentally friendly and atom-efficient oxidant in order to gain mechanistic insights into these novel transformations. In particular, we have focused on clarifying the nature of the high-valent iron oxidants likely to be involved in these transformations.

  5. Microbially Induced Iron Oxidation: What, Where, How

    Energy Technology Data Exchange (ETDEWEB)

    SCHIERMEYER,ELISA M.; PROVENCIO,PAULA P.; NORTHUP,DIANA E.

    2000-08-15

    From the results of the different bacterial cells seen, it is fairly certain that Gallionella is present because of the bean-shaped cells and twisted stalks found with the TEM. The authors cannot confirm, though, what other iron-oxidizing genera exist in the tubes, since the media was only preferential and not one that isolated a specific genus of bacteria. Based on the environment in which they live and the source of the water, they believe their cultures contain Gallionella, Leptothrix, and possibly Crenothrix and Sphaerotilus. They believe the genus Leptothrix rather than Sphaerotilus exist in the tubes because the water source was fresh, unlike the polluted water in which Sphaerotilus are usually found. The TEM preparations worked well. The cryogenic method rapidly froze the cells in place and allowed them to view their morphology. The FAA method, as stated previously, was the best of the three methods because it gave the best contrast. The gluteraldehyde samples did not come out as well. It is possible that the gluteraldehyde the authors prepared was still too concentrated and did not mix well. Although these bacteria were collected from springs and then cultured in an environment containing a presumably pure iron-bearing metal, it seems the tube already containing Manganese Gradient Medium could be used with a piece of metal containing these bacteria. A small piece of corroding metal could then be inserted into the test tube and cultured to study the bacteria.

  6. Multiple hearth furnace for reducing iron oxide

    Science.gov (United States)

    Brandon, Mark M [Charlotte, NC; True, Bradford G [Charlotte, NC

    2012-03-13

    A multiple moving hearth furnace (10) having a furnace housing (11) with at least two moving hearths (20) positioned laterally within the furnace housing, the hearths moving in opposite directions and each moving hearth (20) capable of being charged with at least one layer of iron oxide and carbon bearing material at one end, and being capable of discharging reduced material at the other end. A heat insulating partition (92) is positioned between adjacent moving hearths of at least portions of the conversion zones (13), and is capable of communicating gases between the atmospheres of the conversion zones of adjacent moving hearths. A drying/preheat zone (12), a conversion zone (13), and optionally a cooling zone (15) are sequentially positioned along each moving hearth (30) in the furnace housing (11).

  7. Washing effect on superparamagnetic iron oxide nanoparticles

    Directory of Open Access Journals (Sweden)

    Laura-Karina Mireles

    2016-06-01

    Full Text Available Much recent research on nanoparticles has occurred in the biomedical area, particularly in the area of superparamagnetic iron oxide nanoparticles (SPIONs; one such area of research is in their use as magnetically directed prodrugs. It has been reported that nanoscale materials exhibit properties different from those of materials in bulk or on a macro scale [1]. Further, an understanding of the batch-to-batch reproducibility and uniformity of the SPION surface is essential to ensure safe biological applications, as noted in the accompanying article [2], because the surface is the first layer that affects the biological response of the human body. Here, we consider a comparison of the surface chemistries of a batch of SPIONs, before and after the supposedly gentle process of dialysis in water.

  8. Ultrafine ferromagnetic iron oxide nanoparticles: Facile synthesis by low temperature decomposition of iron glycerolate

    Energy Technology Data Exchange (ETDEWEB)

    Bartůněk, Vilém, E-mail: vilem.bartunek@vscht.cz [Department of Inorganic Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology, Technická 5, 166 28 Prague 6 (Czech Republic); Průcha, David [Department of Inorganic Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology, Technická 5, 166 28 Prague 6 (Czech Republic); Švecová, Marie [Department of Analytical Chemistry, Faculty of Chemical Engineering, University of Chemistry and Technology, Technická 5, 166 28 Prague 6 (Czech Republic); Ulbrich, Pavel [Department of Biochemistry and Microbiology, Faculty of Food and Biochemical Technology, University of Chemistry and Technology, Technická 3, 166 28 Prague 6 (Czech Republic); Huber, Štěpán; Sedmidubský, David; Jankovský, Ondřej [Department of Inorganic Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology, Technická 5, 166 28 Prague 6 (Czech Republic)

    2016-09-01

    We synthesized dark colored ultrafine – sub 10 nm iron oxide nanoparticles by a facile and low temperature process based on thermal decomposition of an affordable precursor – iron glycerolate. Simultaneous thermal analysis (STA) was used to study the thermal behaviour during the decomposition. The iron glycerolate was thoroughly analysed by various methods. The size of the iron nanoparticles was determined from XRD patterns and by transmission electron microscopy (TEM) and their composition has been confirmed by XPS. Magnetic properties of the nanoparticles were studied by vibrating sample magnetometry. The prepared single phase material exhibiting ferromagnetic properties is usable in a wide range of applications and may be suitable even for large scale industrial applications. - Highlights: • Iron glycerolate prepared and characterised. • Iron oxide nanoparticles prepared by thermal decomposition of iron glycerolate. • STA used to study the decomposition. • Products characterised by XRD, XPS, FT-IR, SEM and TEM. • Magnetic behaviour of monophasic samples determined.

  9. Core/shell structured iron/iron-oxide nanoparticles as excellent MRI contrast enhancement agents

    Energy Technology Data Exchange (ETDEWEB)

    Khurshid, Hafsa, E-mail: hkhurshi@udel.edu [Department of Physics and Astronomy, University of Delaware, 217 sharp lab, Newark, DE 19716 (United States); Hadjipanayis, Costas G. [Department of Neurological Surgery, Emory University School of Medicine Atlanta, GA 30322 (United States); Chen, Hongwei [Department of Radiology, Emory University School of Medicine Atlanta, GA 30322 (United States); Li, Wanfeng [Department of Physics and Astronomy, University of Delaware, 217 sharp lab, Newark, DE 19716 (United States); Mao, Hui [Department of Radiology, Emory University School of Medicine Atlanta, GA 30322 (United States); Machaidze, Revaz [Department of Neurological Surgery, Emory University School of Medicine Atlanta, GA 30322 (United States); Tzitzios, Vasilis [Institute of Materials Science, “Demokritos” 15310 Athens (Greece); Hadjipanayis, George C. [Department of Physics and Astronomy, University of Delaware, 217 sharp lab, Newark, DE 19716 (United States)

    2013-04-15

    We report the use of metallic iron-based nanoparticles for magnetic resonance imaging (MRI) applications. Core/shell structured iron-based nanoparticles prepared by thermally decomposing organo-metallic compounds of iron at high temperature in the presence of hydrophobic surfactants were coated and stabilized in the aqueous solvent using the newly developed polysiloxane PEO–b–PγMPS (poly(ethylene oxide)–block–poly (γ methacryloxypropyl trimethyl oxysilane)) diblock copolymers. Particles are well suspended in water and retain their core–shell morphology after coating with the copolymer. In comparison to the conventionally used iron-oxide nanoparticles, core/shell structured iron/iron-oxide nanoparticles offer a much stronger T{sub 2} shortening effect than that of iron-oxide with the same core size due to their better magnetic properties. -- Highlights: ► Core/shell Fe/Fe-oxide nanoparticles were synthesized by organo-metallic synthesis. ► Water dispersibility was obtained by coating particles with a polysiloxane diblock copolymer. ► In comparison to Fe-oxide, Fe/Fe-oxide nanoparticles offer a much stronger T{sub 2} shortening effect.

  10. Formation of silica iron oxide glasses

    Science.gov (United States)

    Al-Bawab, Abeer F.

    The microemulsion-gel method was developed as an alternative process in the production of room temperature glasses. This method is based on the formation of a microemulsion, to which is added a metal alkoxide that undergoes hydrolysis and condensation to form an oxide network, which is dried into glass. The goal of this work is to understand the sol-gel process upon addition of hydrate metal salts. The thermal transitions of the silica containing ferric nitrate hydrate were examined by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). Using infrared (IR) spectroscopy and X-ray diffraction (XRD). The glasses with a less than 30 mol % iron nitrate were amorphous, while those higher concentration were crystalline. Based on XRD the thermal transitions did not alter the crystallinity. The IR spectra indicated the existence of Si-O-Fe bonds. Thermal analysis indicated similar transitions as exhibited by pure iron nitrate with minor modifications due to interactions with the silica. The reaction between tetraethoxysilane and chloral hydrate in ethanol was followed by NMR of the sp{29}Si nucleus at two different pHs. The sp{29}Si NMR spectra were similar to those reported for the reactions in alcohol between tetraethoxysilane and water of low pH, and for the reactions in the presence of inorganic hydrate. At pH 4, monomene silicon species were detected where at pH 2 the reaction was sufficiently rapid that multi hydroxy monomers were not detected as expected from the catalysts. The reaction proceeded without adding water. The reaction between aluminum chloride and methoxydimethyloctylsilane was investigated at room temperature using NMR and IR spectroscopy in addition to a molecular weight determination from the freezing point reduction in benzene. The structure as deduced from the experimental results was found to be a dimer containing two silicon atoms and two aluminum atoms of which the latter were tetrahedrally coordinated.

  11. Application of novel iron core/iron oxide shell nanoparticles to sentinel lymph node identification

    Science.gov (United States)

    Cousins, Aidan; Howard, Douglas; Henning, Anna M.; Nelson, Melanie R. M.; Tilley, Richard D.; Thierry, Benjamin

    2015-12-01

    Current `gold standard' staging of breast cancer and melanoma relies on accurate in vivo identification of the sentinel lymph node. By replacing conventional tracers (dyes and radiocolloids) with magnetic nanoparticles and using a handheld magnetometer probe for in vivo identification, it is believed the accuracy of sentinel node identification in nonsuperficial cancers can be improved due to increased spatial resolution of magnetometer probes and additional anatomical information afforded by MRI road-mapping. By using novel iron core/iron oxide shell nanoparticles, the sensitivity of sentinel node mapping via MRI can be increased due to an increased magnetic saturation compared to traditional iron oxide nanoparticles. A series of in vitro magnetic phantoms (iron core vs. iron oxide nanoparticles) were prepared to simulate magnetic particle accumulation in the sentinel lymph node. A novel handheld magnetometer probe was used to measure the relative signals of each phantom, and determine if clinical application of iron core particles can improve in vivo detection of the sentinel node compared to traditional iron oxide nanoparticles. The findings indicate that novel iron core nanoparticles above a certain size possess high magnetic saturation, but can also be produced with low coercivity and high susceptibility. While some modification to the design of handheld magnetometer probes may be required for particles with large coercivity, use of iron core particles could improve MRI and magnetometer probe detection sensitivity by up to 330 %.

  12. Biogenic Fabrication of Iron/Iron Oxide Nanoparticles and Their Application

    Science.gov (United States)

    Siddiqi, Khwaja Salahuddin; ur Rahman, Aziz; Tajuddin; Husen, Azamal

    2016-11-01

    Enshrined in this review are the biogenic fabrication and applications of coated and uncoated iron and iron oxide nanoparticles. Depending on their magnetic properties, they have been used in the treatment of cancer, drug delivery system, MRI, and catalysis and removal of pesticides from potable water. The polymer-coated iron and iron oxide nanoparticles are made biocompatible, and their slow release makes them more effective and lasting. Their cytotoxicity against microbes under aerobic/anaerobic conditions has also been discussed. The magnetic moment of superparamagnetic iron oxide nanoparticles changes with their interaction with biomolecules as a consequence of which their size decreases. Their biological efficacy has been found to be dependent on the shape, size, and concentration of these nanoparticles.

  13. Neutrophilic iron oxidizers adapted to highly oxic environments

    DEFF Research Database (Denmark)

    Gülay, Arda; Musovic, Sanin; Albrechtsen, Hans-Jørgen

    oxidation of iron would be retarded. For that reason, no attempts have been documented to describe the density and diversity of iron oxidizing bacteria (FeOB) in oxic neutrophilic environments. Under low temperatures (5 to 10°C) conditions, as typically found in groundwater, extremely low rates of chemical...... indicate that neutrophilic iron oxidizers in highly oxic environments like drinking water treatment systems can be abundant (5 E+04 to 7 E+05 cells per gram of wet sand material). It was furthermore observed that the diversity of the cultivated dominant iron oxidizers differs substantially from those...... technique, and dominant bands were isolated and sequenced for identification of dominant enrichment members. Enrichment were microscopically examined via CSLM in combination with FeOB specific or generic cytostains to verify enrichments, check cell morphologies and quantify cell densities. Our results...

  14. Magnetic Iron Oxide Nanoparticles: Synthesis and Surface Functionalization Strategies

    Directory of Open Access Journals (Sweden)

    He Quanguo

    2008-01-01

    Full Text Available Abstract Surface functionalized magnetic iron oxide nanoparticles (NPs are a kind of novel functional materials, which have been widely used in the biotechnology and catalysis. This review focuses on the recent development and various strategies in preparation, structure, and magnetic properties of naked and surface functionalized iron oxide NPs and their corresponding application briefly. In order to implement the practical application, the particles must have combined properties of high magnetic saturation, stability, biocompatibility, and interactive functions at the surface. Moreover, the surface of iron oxide NPs could be modified by organic materials or inorganic materials, such as polymers, biomolecules, silica, metals, etc. The problems and major challenges, along with the directions for the synthesis and surface functionalization of iron oxide NPs, are considered. Finally, some future trends and prospective in these research areas are also discussed.

  15. Iron Oxide Nanocrystals for Magnetic Hyperthermia Applications

    Directory of Open Access Journals (Sweden)

    Dale L. Huber

    2012-05-01

    Full Text Available Magnetic nanocrystals have been investigated extensively in the past several years for several potential applications, such as information technology, MRI contrast agents, and for drug conjugation and delivery. A specific property of interest in biomedicine is magnetic hyperthermia—an increase in temperature resulting from the thermal energy released by magnetic nanocrystals in an external alternating magnetic field. Iron oxide nanocrystals of various sizes and morphologies were synthesized and tested for specific losses (heating power using frequencies of 111.1 kHz and 629.2 kHz, and corresponding magnetic field strengths of 9 and 25 mT. Polymorphous nanocrystals as well as spherical nanocrystals and nanowires in paramagnetic to ferromagnetic size range exhibited good heating power. A remarkable 30 °C temperature increase was observed in a nanowire sample at 111 kHz and magnetic field of 25 mT (19.6 kA/m, which is very close to the typical values of 100 kHz and 20 mT used in medical treatments.

  16. Selenium sorption and isotope fractionation: Iron(III) oxides versus iron(II) sulfides

    NARCIS (Netherlands)

    Mitchell, K.; Couture, R.-M.; Johnson, T.M.; Mason, P.R.D.; Van Cappellen, P.

    2013-01-01

    Sorption and reduction are important processes influencing the environmental mobility and cycling of Se. In this study, we determined the rates of reaction and isotopic fractionations of Se(IV) and Se(VI) during sorption to iron oxides (2-line ferrihydrite, hematite and goethite) and iron sulfides (

  17. Iron Oxide Silica Derived from Sol-Gel Synthesis

    Directory of Open Access Journals (Sweden)

    João Carlos Diniz da Costa

    2011-02-01

    Full Text Available In this work we investigate the effect of iron oxide embedded in silica matrices as a function of Fe/Si molar ratio and sol pH. To achieve homogeneous dispersion of iron oxide particles, iron nitrate nonahydrate was dissolved in hydrogen peroxide and was mixed with tetraethyl orthosilicate and ethanol in a sol-gel synthesis method. Increasing the calcination temperature led to a reduction in surface area, although the average pore radius remained almost constant at about 10 Å, independent of the Fe/Si molar ratio or sol pH. Hence, the densification of the matrix was accompanied by similar reduction in pore volume. However, calcination at 700 °C resulted in samples with similar surface area though the iron oxide content increased from 5% to 50% Fe/Si molar ratio. As metal oxide particles have lower surface area than polymeric silica structures, these results strongly suggest that the iron oxides opposed the silica structure collapse. The effect of sol pH was found to be less significant than the Fe/Si molar ratio in the formation of molecular sieve structures derived from iron oxide silica.

  18. High pressure Moessbauer spectroscopy of perovskite iron oxide

    CERN Document Server

    Nasu, S; Morimoto, S; Kawakami, T; Kuzushita, K; Takano, M

    2003-01-01

    High-pressure sup 5 sup 7 Fe Moessbauer spectroscopy using a diamond anvil cell has been performed for perovskite iron oxides SrFeO sub 3 , CaFeO sub 3 and La sub 1 sub / sub 3 Sr sub 2 sub / sub 3 O sub 3. The charge states and the magnetic dependency to pressure were determined. Pressure magnetic phase diagrams of these perovskite iron oxides are determined up to about 70 GPa. To be clear the magnetic ordered state, they are measured up to 7.8 T external magnetic fields at 4.5K. The phase transition of these perovskite oxides to ferromagnetisms with high magnetic ordered temperature is observed. In higher pressure, high spin-low spin transition of oxides besides CaFeO sub 3 is generated. The feature of Moessbauer spectroscopy, perovskite iron oxide and Moessbauer spectroscopy under high pressure are explained. (S.Y.)

  19. Iron accumulation with age, oxidative stress and functional decline.

    Directory of Open Access Journals (Sweden)

    Jinze Xu

    Full Text Available Identification of biological mediators in sarcopenia is pertinent to the development of targeted interventions to alleviate this condition. Iron is recognized as a potent pro-oxidant and a catalyst for the formation of reactive oxygen species in biological systems. It is well accepted that iron accumulates with senescence in several organs, but little is known about iron accumulation in muscle and how it may affect muscle function. In addition, it is unclear if interventions which reduced age-related loss of muscle quality, such as calorie restriction, impact iron accumulation. We investigated non-heme iron concentration, oxidative stress to nucleic acids in gastrocnemius muscle and key indices of sarcopenia (muscle mass and grip strength in male Fischer 344 X Brown Norway rats fed ad libitum (AL or a calorie restricted diet (60% of ad libitum food intake starting at 4 months of age at 8, 18, 29 and 37 months of age. Total non-heme iron levels in the gastrocnemius muscle of AL rats increased progressively with age. Between 29 and 37 months of age, the non-heme iron concentration increased by approximately 200% in AL-fed rats. Most importantly, the levels of oxidized RNA in gastrocnemius muscle of AL rats were significantly increased as well. The striking age-associated increase in non-heme iron and oxidized RNA levels and decrease in sarcopenia indices were all attenuated in the calorie restriction (CR rats. These findings strongly suggest that the age-related iron accumulation in muscle contributes to increased oxidative damage and sarcopenia, and that CR effectively attenuates these negative effects.

  20. Dextran-modified iron oxide nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Jií; Hradil

    2007-01-01

    [1]Anger,S.,Caldwell,K.,Mehnert,W.,& Muller,R.(1999).Coating of nanoparticles:Analysis of adsorption using sedimentation field-flow fractionation(SdFFF).Proceedings of International Symposium of Controlled Release of Bioactivated Materials,26,599-600.[2]Bonnemain,B.(1998).Superparamagnetic agents in magnetic resonance imaging:Physicochemical characteristics and clinical applications-A review.Journal of Drug Targeting,6(3),167-174.[3]Bootz,A.,Vogel,V.,Schubert,D.,& Kreuter,J.(2004).Comparison of scanning electron microscopy,dynamic light scattering and analytical ultracentrifugation for the sizing of poly(butyl cyanoacrylate) nanoparticles.European Journal of Pharmaceutics and Biopharmaceutics,57(2),369-375.[4]Browarzik,D.(1997).Continuous kinetics of dextran degradation.Journal of Macromolecular Science Pure and Applied Chemistry,34(3),397-404.[5]Cabasso,I.,& Yuan,Y.(1996).Nanoparticles in polymer and polymer dendrimers.In J.Fendler & I.Dekany (Eds.),NATO ASI Series.Part 18Nanoparticles in Solids and Solutions (pp.131-153).[6]Chastellain,M.,Petri,A.,& Hofmann,H.(2004).Particle size investigation of a multistep synthesis of PVA coated superparamagnetic nanoparticles.Journal of Colloid Interface Science,278(2),353-360.[7]Chmela,E.,Tijssen,R.,Blom,M.T.,Gardeniers,H.J.G.E.,& van den Berg,A.(2002).A chip system for size separation of macromolecules and particles by hydrodynamic chromatography.Analytical Chemistry,74(14),3470-3475.[8]Confer,D.R.,& Logan,B.E.(1997).Molecular weight distribution of hydrolysis product during the biodegradation of model macromolecules in suspended and biofilm cultures.Ⅱ:Dextran and dextrin.Water Research,31(9),2137-2145.[9]Griffiths,C.H.,O'Horo,M.P.,& Smith,T.W.(1979).The structure,magnetic characterization and oxidation of colloidal iron dispersions.Journal of Applied Physics,50(11),7108-7115.[10]Gupta,A.K.,& Gupta,M.(2005).Synthesis and surface engineering of iron oxide nanoparticles for biomedical applications.Biomaterials,26

  1. Stem cell tracking using iron oxide nanoparticles

    Directory of Open Access Journals (Sweden)

    Bull E

    2014-03-01

    Full Text Available Elizabeth Bull,1 Seyed Yazdan Madani,1 Roosey Sheth,1 Amelia Seifalian,1 Mark Green,2 Alexander M Seifalian1,31UCL Centre for Nanotechnology and Regenerative Medicine, Division of Surgery and Interventional Science, University College London, London, 2Department of Physics, King’s College London, Strand Campus, London, UK; 3Royal Free London National Health Service Foundation Trust Hospital, London, UKAbstract: Superparamagnetic iron oxide nanoparticles (SPIONs are an exciting advancement in the field of nanotechnology. They expand the possibilities of noninvasive analysis and have many useful properties, making them potential candidates for numerous novel applications. Notably, they have been shown that they can be tracked by magnetic resonance imaging (MRI and are capable of conjugation with various cell types, including stem cells. In-depth research has been undertaken to establish these benefits, so that a deeper level of understanding of stem cell migratory pathways and differentiation, tumor migration, and improved drug delivery can be achieved. Stem cells have the ability to treat and cure many debilitating diseases with limited side effects, but a main problem that arises is in the noninvasive tracking and analysis of these stem cells. Recently, researchers have acknowledged the use of SPIONs for this purpose and have set out to establish suitable protocols for coating and attachment, so as to bring MRI tracking of SPION-labeled stem cells into common practice. This review paper explains the manner in which SPIONs are produced, conjugated, and tracked using MRI, as well as a discussion on their limitations. A concise summary of recently researched magnetic particle coatings is provided, and the effects of SPIONs on stem cells are evaluated, while animal and human studies investigating the role of SPIONs in stem cell tracking will be explored.Keywords: stem cells, nanoparticle, magnetic

  2. One step paired electrochemical synthesis of iron and iron oxide nanoparticles

    Directory of Open Access Journals (Sweden)

    Ordoukhanian Juliet

    2016-09-01

    Full Text Available In this study, a new one step paired electrochemical method is developed for simultaneous synthesis of iron and iron oxide nanoparticles. iron and iron oxide are prepared as cathodic and anodic products from iron (ii sulfate aqueous solution in a membrane divided electrolytic cell by the pulsed current electrosynthesis. Because of organic solvent-free and electrochemical nature of the synthesis, the process could be considered as green and environmentally friendly. The reduction of energy consumption and low cost are the other significant advantages of this new method that would have a great application potential in the chemical industry. The nanostructure of prepared samples was characterized by Fourier transform infrared spectroscopy (FT-IR, X-ray diffraction (XRD, scanning electron microscopy (SEM and transmission electron microscopy (TEM. The magnetic properties were studied by vibrating sample magnetometer (VsM.

  3. Preparation of iron oxides using ammonium iron citrate precursor: Thin films and nanoparticles

    Science.gov (United States)

    Park, Sangmoon

    2009-09-01

    Ammonium iron citrate (C 6H 8O 7·nFe ·nH 3N) was used as a precursor for preparing both iron-oxide thin films and nanoparticles. Thin films of iron oxides were fabricated on silicon (111) substrate using a successive-ionic-layer-adsorption-and-reaction (SILAR) method and subsequent hydrothermal or furnace annealing. Atomic force microscopy (AFM) images of the iron-oxide films obtained under various annealing conditions show the changes of the micro-scale surface structures and the magnetic properties. Homogenous Fe 3O 4 nanoparticles around 4 nm in diameter were synthesized by hydrothermal reduction method at low temperature and investigated using transmission electron microscopy (TEM).

  4. Controlled oxidation of iron nanoparticles in chemical vapour synthesis

    Science.gov (United States)

    Ruusunen, Jarno; Ihalainen, Mika; Koponen, Tarmo; Torvela, Tiina; Tenho, Mikko; Salonen, Jarno; Sippula, Olli; Joutsensaari, Jorma; Jokiniemi, Jorma; Lähde, Anna

    2014-02-01

    In the present study, iron oxide nanoparticles (primary particle size of 80-90 nm) with controlled oxidation state were prepared via an atmospheric pressure chemical vapour synthesis (APCVS) method. Iron pentacarbonyl [Fe(CO)5], a precursor material, was thermally decomposed to iron in the APCVS reactor. Subsequently, the iron was oxidized with controlled amount of oxygen in the reactor to produce nearly pure magnetite or haematite particles depending on the oxygen concentration. Size, morphology and crystal structure of the synthesized nanoparticles were studied with scanning mobility particle sizer (SMPS), transmission electron microscopy (TEM) and X-ray diffraction (XRD). In addition, thermodynamic equilibrium calculations and computational fluid dynamics model were used to predict the oxidation state of the iron oxides and the reaction conditions during mixing. Aggregates of crystalline particles were formed, determined as magnetite at the oxygen volumetric fraction of 0.1 % and haematite at volumetric fraction of 0.5 %, according to the XRD. The geometric mean electrical mobility diameter of the aggregates increased from 110 to 155 nm when the volumetric fraction of oxygen increased from 0.1 to 0.5 %, determined using the SMPS. The aggregates were highly sintered based on TEM analyses. As a conclusion, APCVS method can be used to produce nearly pure crystalline magnetite or haematite nanoparticles with controlled oxidation in a continuous one-stage gas-phase process.

  5. Iron oxide nanoparticle synthesis in aqueous and membrane systems for oxidative degradation of trichloroethylene from water

    Energy Technology Data Exchange (ETDEWEB)

    Gui Minghui; Smuleac, Vasile [University of Kentucky, Department of Chemical and Materials Engineering (United States); Ormsbee, Lindell E. [University of Kentucky, Department of Civil Engineering (United States); Sedlak, David L. [University of California at Berkeley, Department of Civil and Environmental Engineering (United States); Bhattacharyya, Dibakar, E-mail: db@engr.uky.edu [University of Kentucky, Department of Chemical and Materials Engineering (United States)

    2012-05-15

    The potential for using hydroxyl radical (OH{sup Bullet }) reactions catalyzed by iron oxide nanoparticles (NPs) to remediate toxic organic compounds was investigated. Iron oxide NPs were synthesized by controlled oxidation of iron NPs prior to their use for contaminant oxidation (by H{sub 2}O{sub 2} addition) at near-neutral pH values. Cross-linked polyacrylic acid (PAA) functionalized polyvinylidene fluoride (PVDF) microfiltration membranes were prepared by in situ polymerization of acrylic acid inside the membrane pores. Iron and iron oxide NPs (80-100 nm) were directly synthesized in the polymer matrix of PAA/PVDF membranes, which prevented the agglomeration of particles and controlled the particle size. The conversion of iron to iron oxide in aqueous solution with air oxidation was studied based on X-ray diffraction, Moessbauer spectroscopy and BET surface area test methods. Trichloroethylene (TCE) was selected as the model contaminant because of its environmental importance. Degradations of TCE and H{sub 2}O{sub 2} by NP surface generated OH{sup Bullet} were investigated. Depending on the ratio of iron and H{sub 2}O{sub 2}, TCE conversions as high as 100 % (with about 91 % dechlorination) were obtained. TCE dechlorination was also achieved in real groundwater samples with the reactive membranes.

  6. Iron oxide nanoparticle synthesis in aqueous and membrane systems for oxidative degradation of trichloroethylene from water

    Science.gov (United States)

    Gui, Minghui; Smuleac, Vasile; Ormsbee, Lindell E.; Sedlak, David L.; Bhattacharyya, Dibakar

    2012-05-01

    The potential for using hydroxyl radical (OH•) reactions catalyzed by iron oxide nanoparticles (NPs) to remediate toxic organic compounds was investigated. Iron oxide NPs were synthesized by controlled oxidation of iron NPs prior to their use for contaminant oxidation (by H2O2 addition) at near-neutral pH values. Cross-linked polyacrylic acid (PAA) functionalized polyvinylidene fluoride (PVDF) microfiltration membranes were prepared by in situ polymerization of acrylic acid inside the membrane pores. Iron and iron oxide NPs (80-100 nm) were directly synthesized in the polymer matrix of PAA/PVDF membranes, which prevented the agglomeration of particles and controlled the particle size. The conversion of iron to iron oxide in aqueous solution with air oxidation was studied based on X-ray diffraction, Mössbauer spectroscopy and BET surface area test methods. Trichloroethylene (TCE) was selected as the model contaminant because of its environmental importance. Degradations of TCE and H2O2 by NP surface generated OH• were investigated. Depending on the ratio of iron and H2O2, TCE conversions as high as 100 % (with about 91 % dechlorination) were obtained. TCE dechlorination was also achieved in real groundwater samples with the reactive membranes.

  7. Oxidation of Silicon and Boron in Boron Containing Molten Iron

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A new process of directly smelting boron steel from boron-containing pig iron has been established. The starting material boron-containing pig iron was obtained from ludwigite ore, which is very abundant in the eastern area of Liaoning Province of China. The experiment was performed in a medium-frequency induction furnace, and Fe2O3 powder was used as the oxidizing agent. The effects of temperature, addition of Fe2O3, basicity, stirring, and composition of melt on the oxidation of silicon and boron were investigated respectively. The results showed that silicon and boron were oxidized simultaneously and their oxidation ratio exceeded 90% at 1 400 ℃. The favorable oxidation temperature of silicon was about 1 300-1 350 C. High oxygen potential of slag and strong stirring enhanced the oxidation of silicon and boron.

  8. Magnetic composites based on hybrid spheres of aluminum oxide and superparamagnetic nanoparticles of iron oxides

    Energy Technology Data Exchange (ETDEWEB)

    Braga, Tiago P. [Langmuir - Laboratorio de Adsorcao e Catalise, Departamento de Quimica Analitica e Fisico-Quimica, Universidade Federal do Ceara, CP 6021, CEP 60455-970 Campus do Pici, Fortaleza (Brazil); Vasconcelos, Igor F. [Departamento de Engenharia Metalurgica e de Materiais, Universidade Federal do Ceara, Fortaleza (Brazil); Sasaki, Jose M. [Laboratorio de Raios X, Departamento de Fisica, Universidade Federal do Ceara, Campus do Pici, Fortaleza, CE (Brazil); Fabris, J.D.; Oliveira, Diana Q.L. de [Departamento de Quimica, Universidade Federal de Minas Gerais, Belo Horizonte (Brazil); Valentini, Antoninho, E-mail: valent@ufc.b [Langmuir - Laboratorio de Adsorcao e Catalise, Departamento de Quimica Analitica e Fisico-Quimica, Universidade Federal do Ceara, CP 6021, CEP 60455-970 Campus do Pici, Fortaleza (Brazil)

    2010-03-15

    Materials containing hybrid spheres of aluminum oxide and superparamagnetic nanoparticles of iron oxides were obtained from a chemical precursor prepared by admixing chitosan and iron and aluminum hydroxides. The oxides were first characterized with scanning electron microscopy, X-ray diffraction, and Moessbauer spectroscopy. Scanning electron microscopy micrographs showed the size distribution of the resulting spheres to be highly homogeneous. The occurrence of nano-composites containing aluminum oxides and iron oxides was confirmed from powder X-ray diffraction patterns; except for the sample with no aluminum, the superparamagnetic relaxation due to iron oxide particles were observed from Moessbauer spectra obtained at 298 and 110 K; the onset six line-spectrum collected at 20 K indicates a magnetic ordering related to the blocking relaxation effect for significant portion of small spheres in the sample with a molar ratio Al:Fe of 2:1.

  9. A chameleon catalyst for nonheme iron-promoted olefin oxidation.

    Science.gov (United States)

    Iyer, Shyam R; Javadi, Maedeh Moshref; Feng, Yan; Hyun, Min Young; Oloo, Williamson N; Kim, Cheal; Que, Lawrence

    2014-11-18

    We report the chameleonic reactivity of two nonheme iron catalysts for olefin oxidation with H2O2 that switch from nearly exclusive cis-dihydroxylation of electron-poor olefins to the exclusive epoxidation of electron-rich olefins upon addition of acetic acid. This switching suggests a common precursor to the nucleophilic oxidant proposed to Fe(III)-η(2)-OOH and electrophilic oxidant proposed to Fe(V)(O)(OAc), and reversible coordination of acetic acid as a switching pathway.

  10. Iron oxide and gold nanoparticles in cancer therapy

    Science.gov (United States)

    Gotman, Irena; Psakhie, Sergey G.; Lozhkomoev, Aleksandr S.; Gutmanas, Elazar Y.

    2016-08-01

    Continuous research activities in the field of nanomedicine in the past decade have, to a great extent, been focused on nanoparticle technologies for cancer therapy. Gold and iron oxide nanoparticles (NP) are two of the most studied inorganic nanomaterials due to their unique optical and magnetic properties. Both types of NPs are emerging as promising systems for anti-tumor drug delivery and for nanoparticle-mediated thermal therapy of cancer. In thermal therapy, localized heating inside tumors or in proximity of tumor cells can be induced, for example, with Au NPs by radiofrequency ablation heating or conversion of photon energy (photothermal therapy) and in iron oxide magnetic NPs by heat generation through relaxation in an alternating magnetic field (magnetic hyperthermia). Furthermore, the superparamagnetic properties of iron oxide nanoparticles have led to their use as potent MRI (magnetic resonance imaging) contrast agents. Surface modification/coating can produce NPs with tailored and desired properties, such as enhanced blood circulation time, stability, biocompatibility and water solubility. To target nanoparticles to specific tumor cells, NPs should be conjugated with targeting moieties on the surface which bind to receptors or other molecular structures on the cell surface. The article presents several approaches to enhancing the specificity of Au and iron oxide nanoparticles for tumor tissue by appropriate surface modification/functionalization, as well as the effect of these treatments on the saturation magnetization value of iron oxide NPs. The use of other nanoparticles and nanostructures in cancer treatment is also briefly reviewed.

  11. Iron-oxidation processes in an electroflocculation (electrocoagulation) cell

    Energy Technology Data Exchange (ETDEWEB)

    Sasson, Moshe Ben, E-mail: mosheinspain@hotmail.com [Department of Soil and Water Sciences, Robert H. Smith Faculty of Agriculture, Food and Environment, Hebrew University of Jerusalem, Rehovot 76100 (Israel); Calmano, Wolfgang [Institute of Environmental Technology and Energy Economics, Technical University of Hamburg-Harburg, 21073 Hamburg (Germany); Adin, Avner [Department of Soil and Water Sciences, Robert H. Smith Faculty of Agriculture, Food and Environment, Hebrew University of Jerusalem, Rehovot 76100 (Israel)

    2009-11-15

    The processes of iron oxidation in an electroflocculation cell were investigated for a pH range of 5-9 and electric currents of 0.05-0.4 A (equivalent current densities of 8.6-69 A/m{sup 2}). At all pH values and electric currents investigated, it was demonstrated and proven that for all practical purposes, the form of iron that dissolves from the anode is Fe{sup 2+} (ferrous). The difference between the amount of theoretical dissolution as calculated by Faraday's law and the amount of observed dissolved iron ions may indicate two phenomena in electrochemical cells. The first is possible dissolution of the anode even without the operation of an electric current; this led to higher theoretical dissolution rates at lower pH. The second is the participation of some of the electrons of the electric current in reactions other than anode dissolution which led to lower theoretical dissolution rates at higher pH. Those other reactions did not lead to an increase in the local oxidation saturation level near the anode and did not affect iron-oxidation rates in the electroflocculation processes. The oxidation rates of the dissolved Fe{sup 2+} (ferrous) to Fe{sup 3+} (ferric) ions in electroflocculation processes were strongly dependent on the pH and were similar to the known oxidation rates of iron in non-electrochemical cells.

  12. Iron

    DEFF Research Database (Denmark)

    Hansen, Jakob Bondo; Moen, I W; Mandrup-Poulsen, T

    2014-01-01

    The interest in the role of ferrous iron in diabetes pathophysiology has been revived by recent evidence of iron as an important determinant of pancreatic islet inflammation and as a biomarker of diabetes risk and mortality. The iron metabolism in the β-cell is complex. Excess free iron is toxic......, but at the same time, iron is required for normal β-cell function and thereby glucose homeostasis. In the pathogenesis of diabetes, iron generates reactive oxygen species (ROS) by participating in the Fenton chemistry, which can induce oxidative damage and apoptosis. The aim of this review is to present...... and discuss recent evidence, suggesting that iron is a key pathogenic factor in both type 1 and type 2 diabetes with a focus on inflammatory pathways. Pro-inflammatory cytokine-induced β-cell death is not fully understood, but may include iron-induced ROS formation resulting in dedifferentiation by activation...

  13. A pentanuclear iron catalyst designed for water oxidation

    Science.gov (United States)

    Okamura, Masaya; Kondo, Mio; Kuga, Reiko; Kurashige, Yuki; Yanai, Takeshi; Hayami, Shinya; Praneeth, Vijayendran K. K.; Yoshida, Masaki; Yoneda, Ko; Kawata, Satoshi; Masaoka, Shigeyuki

    2016-02-01

    Although the oxidation of water is efficiently catalysed by the oxygen-evolving complex in photosystem II (refs 1 and 2), it remains one of the main bottlenecks when aiming for synthetic chemical fuel production powered by sunlight or electricity. Consequently, the development of active and stable water oxidation catalysts is crucial, with heterogeneous systems considered more suitable for practical use and their homogeneous counterparts more suitable for targeted, molecular-level design guided by mechanistic understanding. Research into the mechanism of water oxidation has resulted in a range of synthetic molecular catalysts, yet there remains much interest in systems that use abundant, inexpensive and environmentally benign metals such as iron (the most abundant transition metal in the Earth’s crust and found in natural and synthetic oxidation catalysts). Water oxidation catalysts based on mononuclear iron complexes have been explored, but they often deactivate rapidly and exhibit relatively low activities. Here we report a pentanuclear iron complex that efficiently and robustly catalyses water oxidation with a turnover frequency of 1,900 per second, which is about three orders of magnitude larger than that of other iron-based catalysts. Electrochemical analysis confirms the redox flexibility of the system, characterized by six different oxidation states between FeII5 and FeIII5; the FeIII5 state is active for oxidizing water. Quantum chemistry calculations indicate that the presence of adjacent active sites facilitates O-O bond formation with a reaction barrier of less than ten kilocalories per mole. Although the need for a high overpotential and the inability to operate in water-rich solutions limit the practicality of the present system, our findings clearly indicate that efficient water oxidation catalysts based on iron complexes can be created by ensuring that the system has redox flexibility and contains adjacent water-activation sites.

  14. Methods of preparing deposits containing iron oxides for recycling

    Directory of Open Access Journals (Sweden)

    T. Lis

    2013-04-01

    Full Text Available The metallurgical industry is one of the largest sources of wastes. Some of them, however, owing to their content of metals such as zinc or iron, may become valuable secondary raw materials. In order to achieve that purpose, they require appropriate preparation. This article provides a discussion on the methods of preparation of scrap from steelworks, namely deposits containing iron oxides, enabling their recycling.

  15. Spectral properties of oxide crystals free of iron ions

    Energy Technology Data Exchange (ETDEWEB)

    Kvapil, J.; Perner, B.; Kvapil, J.; Manek, B.; Kubelka, J.; Blazek, K. (Monokrystaly, Turnov (Czechoslovakia)); Austrata, R.; Schauer, P. (Czechoslovak Academy of Sciences, Brno. Inst. of Scientific Instruments); Vitamvas, Z. (Technical Univ., Liberec (Czechoslovakia))

    1982-07-01

    Al/sub 2/O/sub 3/ and YAG crystals were purified from traces of iron by the growth in reducing atmosphere. Luminescence output of such materials was substantially increased, but some undesirable properties as transient colour centre formation in YAG:Nd and low damage threshold of ruby laser rods were observed. Minimum concentration of iron ions which drastically change spectral properties of oxide crystals seems to be

  16. Gold-Iron Oxide Catalyst for CO Oxidation: Effect of Support Structure

    Directory of Open Access Journals (Sweden)

    Hui-Zhen Cui

    2016-03-01

    Full Text Available Gold-iron oxide (Au/FeOx is one of the highly active catalysts for CO oxidation, and is also a typical system for the study of the chemistry of gold catalysis. In this work, two different types of iron oxide supports, i.e., hydroxylated (Fe_OH and dehydrated iron oxide (Fe_O, have been used for the deposition of gold via a deposition-precipitation (DP method. The structure of iron oxide has been tuned by either selecting precipitated pH of 6.7–11.2 for Fe_OH or changing calcination temperature of from 200 to 600 °C for Fe_O. Then, 1 wt. % Au catalysts on these iron oxide supports were measured for low-temperature CO oxidation reaction. Both fresh and used samples have been characterized by multiple techniques including transmission electron microscopy (TEM and high-resolution TEM (HRTEM, X-ray diffraction (XRD, X-ray photoelectron spectroscopy (XPS, X-ray absorption near edge structure (XANES and temperature-programmed reduction by hydrogen (H2-TPR. It has been demonstrated that the surface properties of the iron oxide support, as well as the metal-support interaction, plays crucial roles on the performance of Au/FeOx catalysts in CO oxidation.

  17. Neutrophilic iron oxidizers adapted to highly oxic environments

    DEFF Research Database (Denmark)

    Gülay, Arda; Musovic, Sanin; Albrechtsen, Hans-Jørgen;

    of iron oxidizing bacterial in the highly oxic environments found in typical rapid sand filters. The neutrophilic FeOB were enriched by the Fe2+/O2 opposing gradient technique and quantified by MPN methodology. Diversity fingerprints of the enrichment cultures were obtained with a 16S rRNA targeted DGGE...... oxidation of iron would be retarded. For that reason, no attempts have been documented to describe the density and diversity of iron oxidizing bacteria (FeOB) in oxic neutrophilic environments. Under low temperatures (5 to 10°C) conditions, as typically found in groundwater, extremely low rates of chemical...... technique, and dominant bands were isolated and sequenced for identification of dominant enrichment members. Enrichment were microscopically examined via CSLM in combination with FeOB specific or generic cytostains to verify enrichments, check cell morphologies and quantify cell densities. Our results...

  18. Multifunctional superparamagnetic iron oxide nanoparticles: promising tools in cancer theranostics.

    Science.gov (United States)

    Santhosh, Poornima Budime; Ulrih, Nataša Poklar

    2013-08-09

    Iron-oxide nanoparticles of small dimensions that have superparamagnetic properties show immense potential to revolutionize the future of cancer theranostics, the combinatorial diagnosis and therapeutic approach towards cancer. Superparamagnetic iron-oxide nanoparticles (SPIONs) have unique magnetic properties, due to which they show excellent tumor-targeting efficiency, and this paves the way for effective personalized cancer treatment. The aim of this review is to focus on the ability of SPIONs to perform multiple roles in the field of cancer biology, such as in diagnosis, monitoring, targeting and therapy. Also, other topics are discussed, including the synthesis of SPIONs, the challenges and recent advances.

  19. Effect of surfactant for magnetic properties of iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Haracz, S. [Faculty of Chemistry, Adam Mickiewicz University, Umultowska 89B, 61-614 Poznań (Poland); Hilgendorff, M. [Freie Universität Berlin, Fachbereich Physik, Arnimalle 14, 14195 Berlin (Germany); Rybka, J.D. [Faculty of Chemistry, Adam Mickiewicz University, Umultowska 89B, 61-614 Poznań (Poland); Giersig, M. [Faculty of Chemistry, Adam Mickiewicz University, Umultowska 89B, 61-614 Poznań (Poland); Freie Universität Berlin, Fachbereich Physik, Arnimalle 14, 14195 Berlin (Germany)

    2015-12-01

    Highlights: • Dynamic behavior of magnetic nanoparticles. • Synthesis of iron oxide nanoparticles. • Effect of surfactant for magnetic properties. - Abstract: For different medical applications nanoparticles (NPs) with well-defined magnetic properties have to be used. Coating ligand can change the magnetic moment on the surface of nanostructures and therefore the magnetic behavior of the system. Here we investigated magnetic NPs in a size of 13 nm conjugated with four different kinds of surfactants. The surface anisotropy and the magnetic moment of the system were changed due to the presence of the surfactant on the surface of iron oxide NPs.

  20. Elucidation of the electrochromic mechanism of nanostructured iron oxides films

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Lobato, M.A.; Martinez, Arturo I.; Castro-Roman, M. [Center for Research and Advanced Studies of the National Polytechnic Institute, Cinvestav Campus Saltillo, Carr. Saltillo-Monterrey Km. 13, Ramos Arizpe, Coah. 25900 (Mexico); Perry, Dale L. [Mail Stop 70A1150, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 (United States); Zarate, R.A. [Departamento de Fisica, Facultad de Ciencias, Universidad Catolica del Norte, Casilla 1280, Antofagasta (Chile); Escobar-Alarcon, L. (Departamento de Fisica, Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico)

    2011-02-15

    Nanostructured hematite thin films were electrochemically cycled in an aqueous solution of LiOH. Through optical, structural, morphological, and magnetic measurements, the coloration mechanism of electrochromic iron oxide thin films was elucidated. The conditions for double or single electrochromic behavior are given in this work. During the electrochemical cycling, it was found that topotactic transformations of hexagonal crystal structures are favored; i.e. {alpha}-Fe{sub 2}O{sub 3} to Fe(OH){sub 2} and subsequently to {delta}-FeOOH. These topotactic redox reactions are responsible for color changes of iron oxide films. (author)

  1. Size-dependent magnetic properties of iron oxide nanoparticles

    Science.gov (United States)

    Patsula, Vitalii; Moskvin, Maksym; Dutz, Silvio; Horák, Daniel

    2016-01-01

    Uniform iron oxide nanoparticles in the size range from 10 to 24 nm and polydisperse 14 nm iron oxide particles were prepared by thermal decomposition of Fe(III) carboxylates in the presence of oleic acid and co-precipitation of Fe(II) and Fe(III) chlorides by ammonium hydroxide followed by oxidation, respectively. While the first method produced hydrophobic oleic acid coated particles, the second one formed hydrophilic, but uncoated, nanoparticles. To make the iron oxide particles water dispersible and colloidally stable, their surface was modified with poly(ethylene glycol) and sucrose, respectively. Size and size distribution of the nanoparticles was determined by transmission electron microscopy, dynamic light scattering and X-ray diffraction. Surface of the PEG-functionalized and sucrose-modified iron oxide particles was characterized by Fourier transform infrared (FT-IR) and Raman spectroscopy and thermogravimetric analysis (TGA). Magnetic properties were measured by means of vibration sample magnetometry and specific absorption rate in alternating magnetic fields was determined calorimetrically. It was found, that larger ferrimagnetic particles showed higher heating performance than smaller superparamagnetic ones. In the transition range between superparamagnetism and ferrimagnetism, samples with a broader size distribution provided higher heating power than narrow size distributed particles of comparable mean size. Here presented particles showed promising properties for a possible application in magnetic hyperthermia.

  2. Iron oxides, dissolved silica, and regulation of marine phosphate concentration

    Science.gov (United States)

    Planavsky, N.; Reinhard, C.; Lyons, T.

    2008-12-01

    Phosphorous concentrations in iron oxide-rich sediments reflect orthophosphate levels in the water column from which iron oxides precipitated. Sediment P/Fe ratios are also strongly influenced by the concentrations of dissolved species that inhibit orthophosphate-to-ferrihydrite sorption, most notably silica. It may, therefore, be possible to use P/Fe ratios in iron oxide-rich sediments to estimate past dissolved P concentrations, if one considers the evolution of the silica cycle. A compilation of Fe and P data in iron oxide-rich sediments through time reveals an increase in P/Fe ratios after the Jurassic. We propose that this trend indicates evolution of the iron-oxide phosphate removal mechanism caused by decreasing levels of sorption inhibition by dissolved silica. The large difference in P/Fe ratios in Cenozoic versus older iron-oxide rich sediments can be linked with Si drawdown caused by the proliferation of siliceous plankton in the Cretaceous. There is also a late Mesozoic or Cenozoic increase in V/Fe ratios, which provides additional evidence for lower ferrihydrite anion sorption efficiency prior to diatom radiation. P/Fe ratios in iron oxide-rich sediments from the early and middle Phanerozoic are comparable to the ratios in iron formations previously presented as evidence for an early Precambrian phosphate crisis (Bjerrum and Canfield, 2002, Nature, 417:159-162). Given the compelling evidence for higher Si concentrations in the Precambrian compared to the Phanerozoic and dissolved P concentrations comparable to modern levels throughout the Phanerozoic, the presented trend of P/Fe ratios suggests dissolved P concentrations were higher in Precambrian than Phanerozoic oceans. High dissolved P levels in the Precambrian may have been linked to inhibited carbonate fluorapatite (CFA) formation as a result of persistently high levels of carbonate supersaturation. Carbonate ion substitution into CFA scales with the ambient carbonate ion activity and increases

  3. Microbial Oxidation of Iron Sulfides in Anaerobic Environments

    DEFF Research Database (Denmark)

    Vaclavkova, Sarka

    . Under anaerobic conditions FeSx serves as an electron donor in nitrate (NO3-) reduction processes. In this PhD thesis, unknown controls of microbial FeSx oxidation by NO3- (MISON), as a potentially important NO3- reducing process, were investigated. The importance of understanding the NO3- removal...... environments including sandy aquifer, freshwater peatland and moderately brackish muddy marine sediment. An apparent salinity limitation of MISON was shown in heavily brackish sediment, where FeSx oxidation was inhibited while other NO3-reduction processes did not appear to be affected by the salinity levels......Abstract (shortened): Iron sulfides (FeSx), representing 0.04-10 % of Danish dry soil weight, oxidize in a presence of oxygen, releasing sulfuric acid and free iron. Environmental impact of FeSx oxidation is commonly seen on agricultural sites cultivated by drainage as acid sulfate soil formation...

  4. Uptake and metabolism of iron oxide nanoparticles in brain cells.

    Science.gov (United States)

    Petters, Charlotte; Irrsack, Ellen; Koch, Michael; Dringen, Ralf

    2014-09-01

    Magnetic iron oxide nanoparticles (IONPs) are used for various applications in biomedicine, for example as contrast agents in magnetic resonance imaging, for cell tracking and for anti-tumor treatment. However, IONPs are also known for their toxic effects on cells and tissues which are at least in part caused by iron-mediated radical formation and oxidative stress. The potential toxicity of IONPs is especially important concerning the use of IONPs for neurobiological applications as alterations in brain iron homeostasis are strongly connected with human neurodegenerative diseases. Since IONPs are able to enter the brain, potential adverse consequences of an exposure of brain cells to IONPs have to be considered. This article describes the pathways that allow IONPs to enter the brain and summarizes the current knowledge on the uptake, the metabolism and the toxicity of IONPs for the different types of brain cells in vitro and in vivo.

  5. From iron coordination compounds to metal oxide nanoparticles

    Directory of Open Access Journals (Sweden)

    Mihail Iacob

    2016-12-01

    Full Text Available Various types, shapes and sizes of iron oxide nanoparticles were obtained depending on the nature of the precursor, preparation method and reaction conditions. The mixed valence trinuclear iron acetate, [Fe2IIIFeIIO(CH3COO6(H2O3]·2H2O (FeAc1, μ3-oxo trinuclear iron(III acetate, [Fe3O(CH3COO6(H2O3]NO3∙4H2O (FeAc2, iron furoate, [Fe3O(C4H3OCOO6(CH3OH3]NO3∙2CH3OH (FeF, iron chromium furoate, FeCr2O(C4H3OCOO6(CH3OH3]NO3∙2CH3OH (FeCrF, and an iron complex with an original macromolecular ligand (FePAZ were used as precursors for the corresponding oxide nanoparticles. Five series of nanoparticle samples were prepared employing either a classical thermal pathway (i.e., thermal decomposition in solution, solvothermal method, dry thermal decomposition/calcination or using a nonconventional energy source (i.e., microwave or ultrasonic treatment to convert precursors into iron oxides. The resulting materials were structurally characterized by wide-angle X-ray diffraction and Fourier transform infrared, Raman, energy-dispersive X-ray, and X-ray fluorescence spectroscopies, as well as thermogravimetric analysis. The morphology was characterized by transmission electron microscopy, atomic force microscopy and dynamic light scattering. The parameters were varied within each route to fine tune the size and shape of the formed nanoparticles.

  6. Moessbauer study of function of magnesium in iron oxide catalysts

    Institute of Scientific and Technical Information of China (English)

    YangJie-Xin; MaoLian-Sheng; 等

    1997-01-01

    Moessbauer spectroscopy has been utilized for studying the action of Mg element in iron oxide catalysts used for the dehydrogenation of ethylbenzene to sytrene.The experimental results show that the presence of opportune amount of Mg can enhance the stability and dispersion of catalysts,i.e.Mg is an sueful structure promoter in this kind of catalysts.

  7. Thermal Plasma Synthesis of Superparamagnetic Iron Oxide Nanoparticles

    NARCIS (Netherlands)

    Lei, P.Y.; Boies, A.M.; Calder, S.A.; Girshick, S.L.

    2012-01-01

    Superparamagnetic iron oxide nanoparticles were synthesized by injecting ferrocene vapor and oxygen into an argon/helium DC thermal plasma. Size distributions of particles in the reactor exhaust were measured online using an aerosol extraction probe interfaced to a scanning mobility particle sizer,

  8. Identification of Spinel Iron Oxide Nanoparticles by 57Fe NMR

    Directory of Open Access Journals (Sweden)

    SangGap Lee

    2011-12-01

    Full Text Available We have synthesized and studied monodisperse iron oxide nanoparticles of smaller than 10 nm to identify between the two spinel phases, magnetite and maghemite. It is shown that 57Fe NMR spectroscopy is a promising tool for distinguishing between the two phases.

  9. Benzene Removal by Iron Oxide Nanoparticles Decorated Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Aamir Abbas

    2016-01-01

    Full Text Available In this paper, carbon nanotubes (CNTs impregnated with iron oxide nanoparticles were employed for the removal of benzene from water. The adsorbents were characterized using scanning electron microscope, X-ray diffraction, BET surface area, and thermogravimetric analysis. Batch adsorption experiments were carried out to study the adsorptive removal of benzene and the effect of parameters such as pH, contact time, and adsorbent dosage. The maximum removal of benzene was 61% with iron oxide impregnated CNTs at an adsorbent dosage 100 mg, shaking speed 200 rpm, contact time 2 hours, initial concentration 1 ppm, and pH 6. However, raw CNTs showed only 53% removal under same experimental conditions. Pseudo-first-order kinetic model was found well to describe the obtained data on benzene removal from water. Initial concentration was varied from 1 to 200 mg/L for isotherms study. Langmuir isotherm model was observed to best describe the adsorption data. The maximum adsorption capacities were 987.58 mg/g and 517.27 mg/g for iron oxide impregnated CNTs and raw CNTs, respectively. Experimental results revealed that impregnation with iron oxide nanoparticles significantly increased the removal efficiency of CNTs.

  10. Biogeochemistry of pyrite and iron sulfide oxidation in marine sediments

    DEFF Research Database (Denmark)

    Schippers, A.; Jørgensen, BB

    2002-01-01

    Pyrite (FeS2) and iron monosulfide (FeS) play a central role in the sulfur and iron cycles of marine sediments, They may be buried in the sediment or oxidized by O-2 after transport by bioturbation to the sediment surface. FeS2 and FeS may also be oxidized within the anoxic sediment in which NO3......-, Fe(III) oxides, or MnO2 are available as potential electron acceptors. In chemical experiments, FeS2 and FeS were oxidized by MnO2 but not with NO3- or amorphous Fe(III) oxide (Schippers and Jørgensen, 2001). Here we also show that in experiments with anoxic sediment slurries, a dissolution of tracer......-marked (FeS2)-Fe-55 occurred with MnO2 but not with NO3- or amorphous Fe(III) oxide as electron acceptor. To study a thermodynamically possible anaerobic microbial FeS, and FeS oxidation with NO3- or amorphous Fe(III) oxide as electron acceptor, more than 300 assays were inoculated with material from several...

  11. Iron oxide nanotubes synthesized via template-based electrodeposition

    Science.gov (United States)

    Lim, Jin-Hee; Min, Seong-Gi; Malkinski, Leszek; Wiley, John B.

    2014-04-01

    Considerable effort has been invested in the development of synthetic methods for the preparation iron oxide nanostructures for applications in nanotechnology. While a variety of structures have been reported, only a few studies have focused on iron oxide nanotubes. Here, we present details on the synthesis and characterization of iron oxide nanotubes along with a proposed mechanism for FeOOH tube formation. The FeOOH nanotubes, fabricated via a template-based electrodeposition method, are found to exhibit a unique inner-surface. Heat treatment of these tubes under oxidizing or reducing atmospheres can produce either hematite (α-Fe2O3) or magnetite (Fe3O4) structures, respectively. Hematite nanotubes are composed of small nanoparticles less than 20 nm in diameter and the magnetization curves and FC-ZFC curves show superparamagnetic properties without the Morin transition. In the case of magnetite nanotubes, which consist of slightly larger nanoparticles, magnetization curves show ferromagnetism with weak coercivity at room temperature, while FC-ZFC curves exhibit the Verwey transition at 125 K.Considerable effort has been invested in the development of synthetic methods for the preparation iron oxide nanostructures for applications in nanotechnology. While a variety of structures have been reported, only a few studies have focused on iron oxide nanotubes. Here, we present details on the synthesis and characterization of iron oxide nanotubes along with a proposed mechanism for FeOOH tube formation. The FeOOH nanotubes, fabricated via a template-based electrodeposition method, are found to exhibit a unique inner-surface. Heat treatment of these tubes under oxidizing or reducing atmospheres can produce either hematite (α-Fe2O3) or magnetite (Fe3O4) structures, respectively. Hematite nanotubes are composed of small nanoparticles less than 20 nm in diameter and the magnetization curves and FC-ZFC curves show superparamagnetic properties without the Morin transition

  12. Oxidation, carburization and/or sulfidation resistant iron aluminide alloy

    Energy Technology Data Exchange (ETDEWEB)

    Sikka, Vinod K.; Deevi, Seetharama C.; Fleischhauer, Grier S.; Hajaligol, Mohammad R.; Lilly, Jr., A. Clifton

    2003-08-19

    The invention relates generally to aluminum containing iron-base alloys useful as electrical resistance heating elements. The aluminum containing iron-base alloys have improved room temperature ductility, electrical resistivity, cyclic fatigue resistance, high temperature oxidation resistance, low and high temperature strength, and/or resistance to high temperature sagging. The alloy has an entirely ferritic microstructure which is free of austenite and includes, in weight %, over 4% Al, .ltoreq.1% Cr and either .gtoreq.0.05% Zr or Zro.sub.2 stringers extending perpendicular to an exposed surface of the heating element or .gtoreq.0.1% oxide dispersoid particles. The alloy can contain 14-32% Al, .ltoreq.2% Ti, .ltoreq.2% Mo, .ltoreq.1% Zr, .ltoreq.1% C, .ltoreq.0.1% B. .ltoreq.30% oxide dispersoid and/or electrically insulating or electrically conductive covalent ceramic particles, .ltoreq.1% rare earth metal, .ltoreq.1% oxygen, .ltoreq.3% Cu, balance Fe.

  13. Iron(III) species formed during iron(II) oxidation and iron-core formation in bacterioferritin of Escherichia coli

    Energy Technology Data Exchange (ETDEWEB)

    Hawkins, C. [Sheffield Univ. (United Kingdom). Dep. of Physics; Treffry, A. [Sheffield Univ. (United Kingdom). Dep. of Molecular Biology and Biotechnology; Mackey, J.; Williams, J.M. [Sheffield Univ. (United Kingdom). Dep. of Physics; Andrews, S.C.; Guest, J.R.; Harrison, P.M. [Sheffield Univ. (United Kingdom). Dep. of Molecular Biology and Biotechnology

    1996-02-01

    This paper describes a preliminary investigation of the mechanisms of Fe(II) oxidation and storage of Fe(III) in the bacterioferritin of Escherichia coli (EcBFR). Using Moessbauer spectroscopy to examine the initial oxidation of iron by EcBFR it is confirmed that this ferritin exhibits ferroxidase activity and is shown that dimeric and monomeric iron species are produced as intermediates. The characteristics of ferroxidase activity in EcBFR is compare d with those of human H-chain ferritin (HuHF) and discuss the different Moessbauer parameters of their dimeric iron with reference to the structures of their di-metal sites. In addition, it is presented preliminary findings suggesting that after an initial {sup b}urst{sup ,} the rate of oxidation is greatly reduced, possibly due to blockage of the ferroxidase centre by bound iron. A new component, not found in HuHF and probably representing a small cluster of Fe(III) atoms, is reported.

  14. Oxidation Potential, Not Crystal Structure, Controls the Oxidation State of Iron in Perovskite

    Science.gov (United States)

    Panero, W. R.; Pigott, J. S.; Watson, H. C.; Scharenberg, M.; Green, H. W.; McComb, D. W.; Williams, R. E.

    2013-12-01

    The mantle's oxidation state has broad implications on the state and evolution of the earth's interior. The relatively high oxidation potential of the upper mantle is such that iron is predominantly Fe2+ with small amounts of Fe3+ . Fe3+ is more stable than Fe2+ in the dominant lower mantle mineral, perovskite, despite the fact that the effect of pressure is to reduce the oxidizing potential of a system. It is therefore suggested that iron undergoes a disproportionation reaction of 3Fe2+ =2Fe3+ +Fe0 , controlled by the crystallography instead of oxidation potential. We crystallized synthetic enstatite glass with 5% Al2O3, 14% FeO, and 3% Fe2O3 in the laser-heated diamond anvil cell at 25-63 GPa and 1700-2800 K. We find that for temperatures nm iron precipitates on grain boundaries. The precipitates have small amounts of dissolved oxygen, but are Mg- and Al- free. We interpret that the stishovite is forming due to the oxidation of the ferric iron to ferrous iron according to (Mg2+,Al3+)(Fe3+,Si4+)O3 +SiO2 + Fe0 while the lower-temperature samples crystallizing as approximately (Mg2+ Fe2+ Al3+ )(Fe3+ Al3+ Si4+ )O3. We observe 2.8(2) Å3 volume expansion of the perovskite and a 28(2) GPa decrease in compressibility of the perovskite relative to the perovskite forming at lower temperature, consistent with the proposed compositions of the perovskites. As the increased temperature increases the oxidation potential of the system, we suggest that the oxidation state of iron in perovskite is dependent on oxidation potential as opposed to perovskite's crystal structure. Transmission Electron Microscopy (TEM) coupled with Electron Energy Loss Spectroscopy (EELS) show iron precipitation on grain boundaries supporting the conclusion. We present a discussion of the results and implications for core formation and lower mantle dynamics.

  15. RECYCLING BLENDS OF WASTE PLASTICS AND BIOMASS AS REDUCING AGENT FOR THE PRODUCTION OF METALLIC IRON FROM IRON OXIDE

    Directory of Open Access Journals (Sweden)

    JAMES RANSFORD DANKWAH

    2013-12-01

    Full Text Available Laboratory studies on the production of metallic iron from iron oxide using blends of palm nut shells (Elaes Guineanses and waste plastics as reducing agent have been performed through experiments conducted in a horizontal tube furnace. Composite pellets were formed from mixtures of iron oxide and carbonaceous materials consisting of chars of palm nut shells (PNS, high density polyethylene (HDPE and two blends of PNS with HDPE. Two sources of iron oxide were utilised in this investigation; reagent grade iron oxide (96.89 % Fe2O3 and EAF slag (47.1 % FeO. The iron oxide-carbonaceous material composites were heated rapidly at 1500°C in a continuous stream of argon and the off gas was analysed continuously using an infrared (IR gas analyser and a gas chromatographic (GC analyser. Elemental analyses of samples of the reduced metal were performed chemically for its carbon and oxygen contents using a LECO carbon/sulphur and oxygen/nitrogen analysers, respectively. The extent of reduction (after ten and fifteen minutes for reagent grade iron oxide and EAF slag, respectively and the level of carburisation were determined for each carbonaceous reductant. The results indicate that carburised metallic iron can be produced effectively from iron oxide using PNS, HDPE and blends of these carbonaceous materials as reductants. The extent of reduction improved significantly when PNS was blended with HDPE.

  16. Oxide Dispersion Strengthened Iron Aluminide by CVD Coated Powders

    Energy Technology Data Exchange (ETDEWEB)

    Asit Biswas Andrew J. Sherman

    2006-09-25

    This I &I Category2 program developed chemical vapor deposition (CVD) of iron, aluminum and aluminum oxide coated iron powders and the availability of high temperature oxidation, corrosion and erosion resistant coating for future power generation equipment and can be used for retrofitting existing fossil-fired power plant equipment. This coating will provide enhanced life and performance of Coal-Fired Boilers components such as fire side corrosion on the outer diameter (OD) of the water wall and superheater tubing as well as on the inner diameter (ID) and OD of larger diameter headers. The program also developed a manufacturing route for readily available thermal spray powders for iron aluminide coating and fabrication of net shape component by powder metallurgy route using this CVD coated powders. This coating can also be applid on jet engine compressor blade and housing, industrial heat treating furnace fixtures, magnetic electronic parts, heating element, piping and tubing for fossil energy application and automotive application, chemical processing equipment , heat exchanger, and structural member of aircraft. The program also resulted in developing a new fabrication route of thermal spray coating and oxide dispersion strengthened (ODS) iron aluminide composites enabling more precise control over material microstructures.

  17. PREPARATION AND CHARACTERIZATION OF IRON OXIDE NANOPARTICLES ON DISACCHARIDE TEMPLATES

    Directory of Open Access Journals (Sweden)

    B ANILREDDY

    2013-09-01

    Full Text Available We report here the preparation of nanoparticles of iron oxide in the presence of polysaccharidetemplates. Interaction between iron sulfate and template has been carried out in aqueous phase,followed by the selective and controlled removal of the template to achieve narrow distribution ofparticle size. Particles of iron oxide obtained have been characterized for their stability in solventmedia, size, size distribution and crystallinity and it was found that when the negative value of thezeta potential increases, particle size decreases. A narrow particle size distribution with D100 = 275nm was obtained with chitosan and starch templates. SEM measurements further confirm the particlesize measurement. Diffuse reflectance UV–VIS spectra values show that the template is completelyremoved from the final iron oxide particles and powder XRD measurements show that the peaks ofthe diffractogram are in agreement with the theoretical data of hematite. The salient observations ofour study shows that there occurs a direct correlation between zeta potential, polydispersity index,band gap energy and particle size. The crystallite size of the particles was found to be 30–35 nm. Alarge negative zeta potential was found to be advantageous for achieving lower particle sizes, as theparticles remained discrete without agglomeration.

  18. The reduction of iron oxides by volatiles in a rotary hearth furnace process: Part II. The reduction of iron oxide/carbon composites

    Science.gov (United States)

    Sohn, I.; Fruehan, R. J.

    2006-04-01

    The reduction of iron oxide/carbon composite pellets with hydrogen at 900 °C to 1000 °C was studied. Compared to hydrogen, the reduction by carbon was negligible at 900 °C and below. However, significant carbon oxidation of the iron oxide/graphite pellets by H2O generated from the reduction of Fe2O3 by H2 was observed. At higher temperatures, reduction by carbon complicates the overall reduction mechanism, with the iron oxide/graphite composite pellet found to be more reactive than the iron oxide/char composite pellet. From the scanning electron micrographs, partially reduced composite pellets showed a typical topochemical interface with an intermediate region between an oxygen-rich unreacted core and an iron-rich outer shell. To determine the possibility of reduction by volatiles, a layer of iron oxide powders was spread on top of a high volatile containing bituminous coal and heated inside a reactor using infra-red radiation. By separating the individual reactions involved for an iron oxide/coal mixture where a complex set of reactions occur simultaneously, it was possible to determine the sole effect of volatile reduction. It was found that the light reducing gases evolve initially and react with the iron oxide, with complex hydrocarbons evolving at the later stages. The volatiles caused about 20 to 50 pct reduction of the iron oxide.

  19. Altering the structure and properties of iron oxide nanoparticles and graphene oxide/iron oxide composites by urea

    Energy Technology Data Exchange (ETDEWEB)

    Naghdi, Samira [Physics department, Bu-Ali Sina University, 65174 Hamedan (Iran, Islamic Republic of); Department of Mechanical Engineering, College of Engineering, Kyung Hee University, 446-701 Yongin (Korea, Republic of); Rhee, Kyong Yop, E-mail: rheeky@khu.ac.kr [Department of Mechanical Engineering, College of Engineering, Kyung Hee University, 446-701 Yongin (Korea, Republic of); Jaleh, Babak [Physics department, Bu-Ali Sina University, 65174 Hamedan (Iran, Islamic Republic of); Park, Soo Jin [Chemistry, Colloge of Natural Science, Inha University, 402-751 Incheon (Korea, Republic of)

    2016-02-28

    Graphical abstract: - Highlights: • Iron oxide (Fe{sub 2}O{sub 3}) nanoparticles were directly grown on graphene oxide (GO) using a facile microwave assistant method. • The effect of urea concentration on Fe{sub 2}O{sub 3} nanoparticles and GO/Fe{sub 2}O{sub 3} composite was examined. • Increasing urea concentration altered the morphology and decreased the particle size. • The increased concentration of urea induced a larger surface area with more active sites in the Fe{sub 2}O{sub 3} nanoparticles. • The increase in urea concentration led to decreased thermal stability of the Fe{sub 2}O{sub 3} nanoparticles. - Abstract: Iron oxide (Fe{sub 2}O{sub 3}) nanoparticles were grown on graphene oxide (GO) using a simple microwave-assisted method. The effects of urea concentration on Fe{sub 2}O{sub 3} nanoparticles and GO/Fe{sub 2}O{sub 3} composite were examined. The as-prepared samples were characterized using X-ray powder diffraction, Raman spectroscopy, and transmission electron microscopy. The Fe{sub 2}O{sub 3} nanoparticles were uniformly developed on GO sheets. The results showed that urea affects both Fe{sub 2}O{sub 3} morphology and particle size. In the absence of urea, the Fe{sub 2}O{sub 3} nanostructures exhibited a rod-like morphology. However, increasing urea concentration altered the morphology and decreased the particle size. The Raman results of GO/Fe{sub 2}O{sub 3} showed that the intensity ratio of D band to G band (I{sub D}/I{sub G}) was decreased by addition of urea, indicating that urea can preserve the GO sheets during synthesis of the composite from exposing more defects. The surface area and thermal stability of GO/Fe{sub 2}O{sub 3} and Fe{sub 2}O{sub 3} were compared using the Brunauer–Emmett–Teller method and thermal gravimetric analysis, respectively. The results showed that the increased concentration of urea induced a larger surface area with more active sites in the Fe{sub 2}O{sub 3} nanoparticles. However, the increase in urea

  20. Oxidative effect of several intravenous iron complexes in the rat.

    Science.gov (United States)

    Bailie, George R; Schuler, Catherine; Leggett, Robert E; Li, Hsin; Li, Hsin-Dat; Patadia, Hiten; Levin, Robert

    2013-06-01

    The objective of this study was to compare the oxidative stress induced in rat internal organs by the administration of the following clinically used intravenous (IV) iron (Fe) containing compounds: iron sucrose (IS), iron dextran (ID), ferric carboxymaltose and ferumoxytol. Groups of six adult rats received 1 mg/kg of each compound weekly for 5 doses. Seven days following the last dose, animals were euthanized and tissue samples of heart, lung, liver, and kidney were obtained, washed in warmed saline and frozen under liquid nitrogen and stored at -80 °C for analysis for nitrotyrosine (NT) and dinitro phenyl (DNP) as markers of oxidative stress. All tissues showed a similar pattern of oxidative stress. All Fe products stimulated an increase in the tissue concentration of both NT and DNP. In general, DNP was stimulated significantly less than NT except for IS. DNP was stimulated to an equal degree except for ID where NT was significantly higher than the NT concentrations in all other Fe compounds. ID produced over 10-fold the concentration of NT than any other Fe. IV Fe compounds present a risk of oxidative stress to a variety of internal organs. However, we found that IS was the least damaging and ID was the worst.

  1. Improved Aeration Process - Catalytic Role Of The Iron Oxides In Arsenic Oxidation And Coprecipitation

    DEFF Research Database (Denmark)

    Kowalski, Krysztof; Søgaard, Erik Gydesen

    2013-01-01

    an improved aeration process that can also help in developing better arsenic removal treatment. The results present advantages of arsenic oxidation in an aeration process in the presence of ferrihydrite surface that have been shown to adsorb arsenic simultaneously to its oxidation. The presence...... of precipitated (ferrihydrite surface) and dissolved iron enhanced arsenic oxidation in comparison to solution with absence of precipitated iron in laboratory scale experiments. However, in the pilot scale studies the adsorption of arsenite on ferrihydrite was found to be the main process occurring during...... implementation of the process in the waterworks that are struggling with arsenic related issues....

  2. High temperature oxidation of iron-chromium alloys

    Energy Technology Data Exchange (ETDEWEB)

    Mikkelsen, Lars

    2003-06-15

    The high temperature oxidation of the ferritic alloy Fe78Cr22 has been investigated in the present work. The effect of small alloying additions of cerium and/or silicon was also investigated. The alloys were oxidized at 973, 1173 and 1373 K in either air or a hydrogen/argon mixture. The various reaction atmospheres contained between 0.02 and 50% water vapour. The oxide scales formed on the various alloys at 973 K consisted of thin chromia layers. The oxide scales grown on the alloys at 1173 K also consisted of a chromia layer. The microstructure of the chromia scales was found to depend on the reaction atmosphere. The chromia scales grown in hydrogen/argon atmospheres formed oxide whiskers and oxide ridges at the surface of the scales, while the chromia scales grown in air formed larger oxide grains near the surface. This difference in oxide microstructure was due to the vaporization of chromium species from the chromia scales grown in air. Two different growth mechanisms are proposed for the growth of oxide whiskers. The growth rate of the chromia scales was independent of the oxygen activity. This is explained by a growth mechanism of the chromia scales, where the growth is governed by the diffusion of interstitial chromium. The addition of silicon to the iron-chromium alloy resulted in the formation of silica particles beneath the chromia scale. The presence of silicon in the alloy was found to decrease the growth rate of the chromia scale. This is explained by a blocking mechanism, where the silica particles beneath the chromia scale partly block the outwards diffusion of chromium from the alloy to the chromia scale. The addition of cerium to the iron-chromium alloy improved the adhesion of the chromia scale to the alloy and decreased the growth rate of chromia. It was observed that the minimum concentration of cerium in the alloy should be 0.3 at.% in order to observe an effect of the cerium addition. The effect of cerium is explained by the &apos

  3. Concurrent repletion of iron and zinc reduces intestinal oxidative damage in iron-and zinc-deficient rats

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    AIM: To understand the interactions between iron and zinc during absorption in iron- and zinc-deficient rats,and their consequences on intestinal oxidant-antioxidant balance.METHODS: Twenty-four weanling Wistar-Kyoto rats fed an iron- and zinc-deficient diet (< 6.5 mg Fe and 4.0 mg Zn/kg diet) for 4 wk were randomly divided into three groups (n = 8, each) and orally gavaged with 4 mg iron, 3.3 mg zinc, or 4 mg iron + 3.3 mg zinc for 2wk. At the last day of repletion, 3 h before the animals were sacrificed, they received either 37 mBq of 55Fe or 65Zn, to study their localization in the intestine, using microautoradiography. Hemoglobin, iron and zinc content in plasma and liver were measured as indicators of iron and zinc status. Duodenal sections were used for immunochemical staining of ferritin and metallothionein.Duodenal homogenates (mitochondrial and cytosolic fractions), were used to assess aconitase activity,oxidative stress, functional integrity and the response of antioxidant enzymes.RESULTS: Concurrent repletion of iron- and zinc-deficient rats showed reduced localization of these minerals compared to rats that were teated with iron or zinc alone;these data provide evidence for antagonistic interactions.This resulted in reduced formation of lipid and protein oxidation products and better functional integrity of the intestinal mucosa. Further, combined repletion lowered iron-associated aconitase activity and ferritin expression,but significantly elevated metallothionein and glutathione levels in the intestinal mucosa. The mechanism of interactions during combined supplementation and its subsequent effects appeared to be due to through modulation of cytosolic aconitase, which in turn influenced the labile iron pool and metallothionein levels, and hence reduced intestinal oxidative damage.CONCLUSION: Concurrent administration of iron and zinc corrects iron and zinc deficiency, and also reduces the intestinal oxidative damage associated with iron

  4. Low Temperature CO oxidation over Iron Oxide Nanoparticles Decorating Internal Structures of a Mesoporous Alumina

    Science.gov (United States)

    Kim, Il Hee; Seo, Hyun Ook; Park, Eun Ji; Han, Sang Wook; Kim, Young Dok

    2017-01-01

    Using a chemical vapor deposition method with regulated sample temperatures under ambient pressure conditions, we were able to fully decorate the internal structure of a mesoporous Al2O3 bead (~1 mm in particle diameter) with iron oxide nanoparticles (with a mean lateral size of less than 1 nm). The iron oxide-decorated Al2O3 showed a high CO oxidation reactivity, even at room temperature. Very little deactivation of the CO oxidation activity was observed with increasing reaction time at ~100 °C. Additionally, this catalyst showed high CO oxidation activity, even after annealing at ~900 °C under atmospheric conditions (i.e., the structure of the catalysts could be maintained under very harsh treatment conditions). We show that our catalysts have potential for application as oxidation catalysts in industrial processes due to the simplicity of their fabrication process as well as the high and stable catalytic performance. PMID:28091561

  5. Thermogravimetric Analysis of the Zinc Concentrates Oxidation Containing Various Iron Compounds

    Directory of Open Access Journals (Sweden)

    Małecki S.

    2014-10-01

    Full Text Available This paper presents the results of oxidation of zinc concentrates containing various iron compounds. Using the thermogravimetry and thermal analysis methods it was shown that the influence of the iron form affects the thermal oxidation process. They influence the rate of, oxidation of zinc sulphide and consequently the resulting rate of oxidation of the concentrate.

  6. Synthesis, Characterization, and Cytotoxicity of Iron Oxide Nanoparticles

    Directory of Open Access Journals (Sweden)

    S. Kanagesan

    2013-01-01

    Full Text Available In order to study the response of human breast cancer cells' exposure to nanoparticle, iron oxide (α-Fe2O3 nanoparticles were synthesized by a simple low temperature combustion method using Fe(NO33·9H2O as raw material. X-ray diffraction studies confirmed that the resultant powders are pure α-Fe2O3. Transmission electron microscopy study revealed the spherical shape of the primary particles, and the size of the iron oxide nanoparticles is in the range of 19 nm. The magnetic hysteresis loops demonstrated that the sample exposed ferromagnetic behaviors with a relatively low coercivity. The cytotoxicity of α-Fe2O3 nanoparticle was also evaluated on human breast cancer cells to address the current deficient knowledge of cellular response to nanoparticle exposure.

  7. Iron aluminide alloy container for solid oxide fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Judkins, Roddie Reagan (Knoxville, TN); Singh, Prabhakar (Export, PA); Sikka, Vinod Kumar (Oak Ridge, TN)

    2000-01-01

    A container for fuel cells is made from an iron aluminide alloy. The container alloy preferably includes from about 13 to about 22 weight percent Al, from about 2 to about 8 weight percent Cr, from about 0.1 to about 4 weight percent M selected from Zr and Hf, from about 0.005 to about 0.5 weight percent B or from about 0.001 to about 1 weight percent C, and the balance Fe and incidental impurities. The iron aluminide container alloy is extremely resistant to corrosion and metal loss when exposed to dual reducing and oxidizing atmospheres at elevated temperatures. The alloy is particularly useful for containment vessels for solid oxide fuel cells, as a replacement for stainless steel alloys which are currently used.

  8. Potential toxicity of superparamagnetic iron oxide nanoparticles (SPION

    Directory of Open Access Journals (Sweden)

    Neenu Singh

    2010-09-01

    Full Text Available Superparamagnetic iron oxide nanoparticles (SPION are being widely used for various biomedical applications, for example, magnetic resonance imaging, targeted delivery of drugs or genes, and in hyperthermia. Although, the potential benefits of SPION are considerable, there is a distinct need to identify any potential cellular damage associated with these nanoparticles. Besides focussing on cytotoxicity, the most commonly used determinant of toxicity as a result of exposure to SPION, this review also mentions the importance of studying the subtle cellular alterations in the form of DNA damage and oxidative stress. We review current studies and discuss how SPION, with or without different surface coating, may cause cellular perturbations including modulation of actin cytoskeleton, alteration in gene expression profiles, disturbance in iron homeostasis and altered cellular responses such as activation of signalling pathways and impairment of cell cycle regulation. The importance of protein–SPION interaction and various safety considerations relating to SPION exposure are also addressed.

  9. Porous Iron oxide nanorods and their photothermal applications

    Science.gov (United States)

    Larsen, George; Huang, Weijie; Zhao, Yiping; Hunyadi Murph, Simona E.

    2016-09-01

    Iron oxide is a unique semiconductor material, either as a single nanoparticle, or as a component of multifunctional nanoparticles. Its desirable properties, abundance, non-toxicity, and excellent magnetic properties make it a valuable for many applications. Porous iron oxide nanorods are able to transduce light into heat through the photothermal effect. Photothermal heating arises from the energy dissipated during light absorption leading to rapid temperature rise in close proximity to the surface of the nanoparticle. The heating effect can be efficiently harnessed to drive/promote different physical phenomena. In this report, we describe the synthesis and properties of porous Fe3O4 for photothermal applications. We then demonstrate their use as photothermally enhanced and recyclable materials for environmental remediation through sorption processes.

  10. Promising iron oxide-based magnetic nanoparticles in biomedical engineering.

    Science.gov (United States)

    Tran, Phuong Ha-Lien; Tran, Thao Truong-Dinh; Vo, Toi Van; Lee, Beom-Jin

    2012-12-01

    For the past few decades biomedical engineering has imprinted its significant impact on the map of science through its wide applications on many other fields. An important example obviously proving this fact is the versatile application of magnetic nanoparticles in theranostics. Due to preferable properties such as biocompatibility, non-toxicity compared to other metal derivations, iron oxide-based magnetic nanoparticles was chosen to be addressed in this review. Aim of this review is to give the readers a whole working window of these magnetic nanoparticles in the current context of science. Thus, preparation of magnetic iron oxide nanoparticles with the so-far techniques, methods of characterizing the nanoparticles as well as their most recent biomedical applications will be stated.

  11. Noble Metal-Iron Oxide Hybrid Nanomaterials: Emerging Applications.

    Science.gov (United States)

    Leung, Ken Cham-Fai; Xuan, Shouhu

    2016-02-01

    This account provides an overview of current research activities that focus on the synthesis and applications of nanomaterials from noble metal (e.g., Au, Ag, Pd) and iron oxide (Fe3O4) hybrids. An introduction to the synthetic strategies that have been developed for generating M-Fe3O4 nanomaterials with different novel structures is presented. Surface functionalization and bioconjugation of these hybrid nanoparticles and nanocomposites are also reviewed. The utilization of the advantageous properties of both noble metals and iron oxide for a variety of applications, such as theranostics, gene delivery, biosensing, cell sorting, bioseparation, and catalysis, is discussed and highlighted. Finally, future trends and perspectives of these sophisticated nanocomposites are outlined. The fundamental requirements underpinning the effective preparation of M-Fex Oy hybrid nanomaterials shed light on the future development of heterogeneous catalysts, nanotheranostics, nanomedicines, and other chemical technologies.

  12. Reactive oxygen species-related activities of nano-iron metal and nano-iron oxides

    Directory of Open Access Journals (Sweden)

    Haohao Wu

    2014-03-01

    Full Text Available Nano-iron metal and nano-iron oxides are among the most widely used engineered and naturally occurring nanostructures, and the increasing incidence of biological exposure to these nanostructures has raised concerns about their biotoxicity. Reactive oxygen species (ROS-induced oxidative stress is one of the most accepted toxic mechanisms and, in the past decades, considerable efforts have been made to investigate the ROS-related activities of iron nanostructures. In this review, we summarize activities of nano-iron metal and nano-iron oxides in ROS-related redox processes, addressing in detail the known homogeneous and heterogeneous redox mechanisms involved in these processes, intrinsic ROS-related properties of iron nanostructures (chemical composition, particle size, and crystalline phase, and ROS-related bio-microenvironmental factors, including physiological pH and buffers, biogenic reducing agents, and other organic substances.

  13. Superparamagnetic iron oxide nanoparticles: magnetic nanoplatforms as drug carriers

    Directory of Open Access Journals (Sweden)

    Wahajuddin

    2012-07-01

    Full Text Available Wahajuddin,1,2 Sumit Arora21Pharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh, 2Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Rae Bareli, IndiaAbstract: A targeted drug delivery system is the need of the hour. Guiding magnetic iron oxide nanoparticles with the help of an external magnetic field to its target is the principle behind the development of superparamagnetic iron oxide nanoparticles (SPIONs as novel drug delivery vehicles. SPIONs are small synthetic γ-Fe2O3 (maghemite or Fe3O4 (magnetite particles with a core ranging between 10 nm and 100 nm in diameter. These magnetic particles are coated with certain biocompatible polymers, such as dextran or polyethylene glycol, which provide chemical handles for the conjugation of therapeutic agents and also improve their blood distribution profile. The current research on SPIONs is opening up wide horizons for their use as diagnostic agents in magnetic resonance imaging as well as for drug delivery vehicles. Delivery of anticancer drugs by coupling with functionalized SPIONs to their targeted site is one of the most pursued areas of research in the development of cancer treatment strategies. SPIONs have also demonstrated their efficiency as nonviral gene vectors that facilitate the introduction of plasmids into the nucleus at rates multifold those of routinely available standard technologies. SPION-induced hyperthermia has also been utilized for localized killing of cancerous cells. Despite their potential biomedical application, alteration in gene expression profiles, disturbance in iron homeostasis, oxidative stress, and altered cellular responses are some SPION-related toxicological aspects which require due consideration. This review provides a comprehensive understanding of SPIONs with regard to their method of preparation, their utility as drug delivery vehicles, and some concerns which need to

  14. Acicular iron nanoparticles protected against sintering with aluminium oxide

    OpenAIRE

    Morales, M. P.; Serna, C. J.; Pozas, R.; Ocaña Jurado, Manuel

    2004-01-01

    [EN] Acicular iron nanoparticles have been obtained by thermal reduction with hydrogen of a goethite precursor protected against sintering with Al cations, either by doping during the synthesis or by a further coating and the relation between microstructure and magnetic properties of the final Fe particles has been studied in order to evaluate the efficiency of both protecting methods. Uniform goethite and Al-doped goethite precursors were prepared by oxidation with air of FeSO4 solu...

  15. Modulated self-reversed magnetic hysteresis in iron oxides

    Science.gov (United States)

    Ma, Ji; Chen, Kezheng

    2017-02-01

    The steadfast rule of a ferromagnetic hysteresis loop claims its saturation positioned within the first and third quadrants, whereas its saturation positioned in the second and fourth quadrants (named as self-reversed magnetic hysteresis) is usually taken as an experimental artifact and is always intentionally ignored. In this report, a new insight in this unique hysteresis phenomenon and its modulation were discussed in depth. Different iron oxides (magnetite, maghemite and hematite) with varying dimensions were soaked in FeCl3 aqueous solution and absorbed Fe3+ cations due to their negative enough surface zeta potentials. These iron oxides@Fe3+ core-shell products exhibit well pronounced self-reversed magnetic hysteresis which concurrently have typical diamagnetic characteristics and essential ferromagnetic features. The presence of pre-magnetized Fe3+ shell and its negatively magnetic exchange coupling with post-magnetized iron-oxide core is the root cause for the observed phenomena. More strikingly, this self-reversed magnetic hysteresis can be readily modulated by changing the core size or by simply controlling Fe3+ concentration in aqueous solution. It is anticipated that this work will shed new light on the development of spintronics, magnetic recording and other magnetically-relevant fields.

  16. Reducing arsenic accumulation in rice grain through iron oxide amendment.

    Science.gov (United States)

    Farrow, Eric M; Wang, Jianmin; Burken, Joel G; Shi, Honglan; Yan, Wengui; Yang, John; Hua, Bin; Deng, Baolin

    2015-08-01

    Effects of soil-arsenic (As), phosphorus and iron oxide on As accumulation in rice grain were investigated. Cultivars that have significantly different sensitivity to As, straighthead-resistant Zhe 733 and straighthead-susceptible Cocodrie, were used to represent different cultivar varieties. The grain accumulation of other elements of concern, selenium (Se), molybdenum (Mo), and cadmium (Cd) was also monitored. Results demonstrated that high soil-As not only resulted in high grain-As, but could also result in high grain-Se, and Zhe 733 had significantly less grain-As than Cocodrie did. However, soil-As did not impact grain-Mo and Cd. Among all elements monitored, iron oxide amendment significantly reduced grain-As for both cultivars, while the phosphate application only reduced grain-Se for Zhe 733. Results also indicated that cultivar type significantly impacted grain accumulation of all monitored trace elements. Therefore, applying iron oxide to As-contaminated land, in addition to choosing appropriate rice cultivar, can effectively reduce the grain accumulation of As.

  17. Versatile ferrofluids based on polyethylene glycol coated iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Brullot, W., E-mail: ward.brullot@fys.kuleuven.be [Department of Chemistry, Katholieke Universiteit Leuven, Celestijnenlaan 200D, 3001 Heverlee, Leuven (Belgium); Reddy, N.K. [Department of Chemical Engineering, Katholieke Universiteit Leuven, Willem de Croylaan 46, 3001 Heverlee, Leuven (Belgium); Wouters, J.; Valev, V.K.; Goderis, B. [Department of Chemistry, Katholieke Universiteit Leuven, Celestijnenlaan 200D, 3001 Heverlee, Leuven (Belgium); Vermant, J. [Department of Chemical Engineering, Katholieke Universiteit Leuven, Willem de Croylaan 46, 3001 Heverlee, Leuven (Belgium); Verbiest, T. [Department of Chemistry, Katholieke Universiteit Leuven, Celestijnenlaan 200D, 3001 Heverlee, Leuven (Belgium)

    2012-06-15

    Versatile ferrofluids based on polyethylene glycol coated iron oxide nanoparticles were obtained by a facile protocol and thoroughly characterized. Superparamagnetic iron oxide nanoparticles synthesized using a modified forced hydrolysis method were functionalized with polyethylene glycol silane (PEG silane), precipitated and dried. These functionalized particles are dispersable in a range of solvents and concentrations depending on the desired properties. Examples of tunable properties are magnetic behavior, optical and magneto-optical response, thermal features and rheological behavior. As such, PEG silane functionalized particles represent a platform for the development of new materials that have broad applicability in e.g. biomedical, industrial or photonic environments. Magnetic, optical, magneto-optical, thermal and rheological properties of several ferrofluids based on PEG coated particles with different concentrations of particles dispersed in low molecular mass polyethylene glycol were investigated, establishing the applicability of such materials. - Highlights: Black-Right-Pointing-Pointer Ferrofluids based on polyethylene glycol coated iron oxide nanoparticles. Black-Right-Pointing-Pointer Magnetic, optical, magneto-optical, thermal and rheological characterization of ferrofluids. Black-Right-Pointing-Pointer Tunable properties of versatile polyethylene glycol stabilized ferrofluids.

  18. Electron uptake by iron-oxidizing phototrophic bacteria

    Energy Technology Data Exchange (ETDEWEB)

    Bose, A; Gardel, EJ; Vidoudez, C; Parra, EA; Girguis, PR

    2014-02-26

    Oxidation-reduction reactions underlie energy generation in nearly all life forms. Although most organisms use soluble oxidants and reductants, some microbes can access solid-phase materials as electron-acceptors or -donors via extracellular electron transfer. Many studies have focused on the reduction of solid-phase oxidants. Far less is known about electron uptake via microbial extracellular electron transfer, and almost nothing is known about the associated mechanisms. Here we show that the iron-oxidizing photoautotroph Rhodopseudomonas palustris TIE-1 accepts electrons from a poised electrode, with carbon dioxide as the sole carbon source/electron acceptor. Both electron uptake and ruBisCo form I expression are stimulated by light. Electron uptake also occurs in the dark, uncoupled from photosynthesis. Notably, the pioABC operon, which encodes a protein system essential for photoautotrophic growth by ferrous iron oxidation, influences electron uptake. These data reveal a previously unknown metabolic versatility of photoferrotrophs to use extracellular electron transfer for electron uptake.

  19. Statement on the validity and robustness of information provided on irradiated iron oxides

    Directory of Open Access Journals (Sweden)

    European Food Safety Authority

    2014-07-01

    Full Text Available Following a Rapid Alert System for Food and Feed (RASFF notification concerning the use of an unauthorised irradiated colouring agent (brown iron oxide as coatings of food supplements, the European Commission asked EFSA to assess the scientific validity and robustness of three documents i two safety assessments from two pharmaceutical companies including information on the manufacturing process of iron oxides, and ii one safety assessment on gamma irradiated iron oxides in food supplements provided by a consultant. According to the supplier of iron oxides and hydroxides (E 172, the aim of the 60Co-gamma irradiation treatment was to eliminate microbiological contamination. Iron oxides and hydroxides (E 172 are authorised food additives in the EU. EFSA noted that the gamma irradiation of iron oxides (yellow, red, black and brown has not been previously evaluated by other Scientific Committees dealing with foodstuffs, pharmaceutical products or cosmetics and that the irradiation doses applied to iron oxides in this particular case are higher than the doses currently authorised in the EU for “other food and food ingredients”. EFSA also noted that some evidence is available in the literature demonstrating a reduction of iron(III to iron(II due to 60Co-gamma irradiation and, that the food additive black iron oxide, as authorised in the EU, contains iron in both (II and (III valence states. Therefore, an increase in the content of divalent iron would not be of safety concern per se. However, EFSA also notes that the information on irradiated iron oxides provided is very limited and insufficient to substantiate the claim that iron oxides are not expected to undergo any chemical transformation upon irradiation. In order to demonstrate the chemical stability of iron oxide during the 60Co-gamma irradiation treatment, EFSA recommends to carry out some further analyses.

  20. Unification of catalytic water oxidation and oxygen reduction reactions: amorphous beat crystalline cobalt iron oxides.

    Science.gov (United States)

    Indra, Arindam; Menezes, Prashanth W; Sahraie, Nastaran Ranjbar; Bergmann, Arno; Das, Chittaranjan; Tallarida, Massimo; Schmeißer, Dieter; Strasser, Peter; Driess, Matthias

    2014-12-17

    Catalytic water splitting to hydrogen and oxygen is considered as one of the convenient routes for the sustainable energy conversion. Bifunctional catalysts for the electrocatalytic oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER) are pivotal for the energy conversion and storage, and alternatively, the photochemical water oxidation in biomimetic fashion is also considered as the most useful way to convert solar energy into chemical energy. Here we present a facile solvothermal route to control the synthesis of amorphous and crystalline cobalt iron oxides by controlling the crystallinity of the materials with changing solvent and reaction time and further utilize these materials as multifunctional catalysts for the unification of photochemical and electrochemical water oxidation as well as for the oxygen reduction reaction. Notably, the amorphous cobalt iron oxide produces superior catalytic activity over the crystalline one under photochemical and electrochemical water oxidation and oxygen reduction conditions.

  1. Microbial iron reduction and methane oxidation in subsurface sediments of the Arabian Sea

    Digital Repository Service at National Institute of Oceanography (India)

    Fernandes, C.E.G.; Judith, M.; Gonsalves, M.J.B.D.; Nazareth, D.R.; Nagarchi, L.; Kamaleson, A.S.

    oxidation. Total bacterial abundance (TC), viable aerobic counts accounting for aerobic and facultative anaerobes (TVCa), viable anaerobic counts (TVCan), methane, sulfate, ferrous [Fe(II], hydroxylamine extractable iron and HCl extractable iron...

  2. Altering the structure and properties of iron oxide nanoparticles and graphene oxide/iron oxide composites by urea

    Science.gov (United States)

    Naghdi, Samira; Rhee, Kyong Yop; Jaleh, Babak; Park, Soo Jin

    2016-02-01

    Iron oxide (Fe2O3) nanoparticles were grown on graphene oxide (GO) using a simple microwave-assisted method. The effects of urea concentration on Fe2O3 nanoparticles and GO/Fe2O3 composite were examined. The as-prepared samples were characterized using X-ray powder diffraction, Raman spectroscopy, and transmission electron microscopy. The Fe2O3 nanoparticles were uniformly developed on GO sheets. The results showed that urea affects both Fe2O3 morphology and particle size. In the absence of urea, the Fe2O3 nanostructures exhibited a rod-like morphology. However, increasing urea concentration altered the morphology and decreased the particle size. The Raman results of GO/Fe2O3 showed that the intensity ratio of D band to G band (ID/IG) was decreased by addition of urea, indicating that urea can preserve the GO sheets during synthesis of the composite from exposing more defects. The surface area and thermal stability of GO/Fe2O3 and Fe2O3 were compared using the Brunauer-Emmett-Teller method and thermal gravimetric analysis, respectively. The results showed that the increased concentration of urea induced a larger surface area with more active sites in the Fe2O3 nanoparticles. However, the increase in urea concentration led to decreased thermal stability of the Fe2O3 nanoparticles. The magnetic properties of Fe2O3 nanoparticles were characterized by a vibrating sample magnetometer and results revealed that the magnetic properties of Fe2O3 nanoparticles are affected by the morphology.

  3. Crystal structure of iron-oxide nanoparticles synthesized from ferritin

    Energy Technology Data Exchange (ETDEWEB)

    Krispin, Michael, E-mail: michael.krispin@physik.uni-augsburg.de; Ullrich, Aladin, E-mail: aladin.ullrich@physik.uni-augsburg.de; Horn, Siegfried, E-mail: horn@physik.uni-augsburg.de [University of Augsburg, Institute of Physics (Germany)

    2012-02-15

    We have investigated the crystal structure of nanosized iron-oxide by X-ray diffraction (XRD), extended X-ray absorption fine structure measurements at the iron K-edge as well as by transmission electron microscopy (TEM). Iron-oxide nanoparticles were produced by thermal treatment of horse spleen ferritin molecules. The structure of these particles was compared to {alpha}-Fe{sub 2}O{sub 3} and {gamma}-Fe{sub 2}O{sub 3} nanopowder references. The thermal treatment of a submonolayer film of ferritin molecules results in pure {gamma}-Fe{sub 2}O{sub 3} nanoparticles, while for films above a certain thickness {alpha}-Fe{sub 2}O{sub 3} and {gamma}-Fe{sub 2}O{sub 3} coexist, exhibiting two different crystallite sizes. TEM shows a characteristic particle diameter of {approx}7 nm for {gamma}-Fe{sub 2}O{sub 3} resulting from thermal treatment of monolayers, consistent with the crystallite size of the {gamma}-phase as obtained from XRD measurements on multi-layered samples. XRD shows the {alpha}-Fe{sub 2}O{sub 3} phase to be characterized by a crystallite size of {approx}34 nm.

  4. Mercury removal in wastewater by iron oxide nanoparticles

    Science.gov (United States)

    Vélez, E.; Campillo, G. E.; Morales, G.; Hincapié, C.; Osorio, J.; Arnache, O.; Uribe, J. I.; Jaramillo, F.

    2016-02-01

    Mercury is one of the persistent pollutants in wastewater; it is becoming a severe environmental and public health problem, this is why nowadays its removal is an obligation. Iron oxide nanoparticles are receiving much attention due to their properties, such as: great biocompatibility, ease of separation, high relation of surface-area to volume, surface modifiability, reusability, excellent magnetic properties and relative low cost. In this experiment, Fe3O4 and γ-Fe2O3 nanoparticles were synthesized using iron salts and NaOH as precipitation agents, and Aloe Vera as stabilizing agent; then these nanoparticles were characterized by three different measurements: first, using a Zetasizer Nano ZS for their size estimation, secondly UV-visible spectroscopy which showed the existence of resonance of plasmon at λmax∼360 nm, and lastly by Scanning Electron Microscopy (SEM) to determine nanoparticles form. The results of this characterization showed that the obtained Iron oxides nanoparticles have a narrow size distribution (∼100nm). Mercury removal of 70% approximately was confirmed by atomic absorption spectroscopy measurements.

  5. Investigation on steelmaking dust recycling and iron oxide red preparing

    Institute of Scientific and Technical Information of China (English)

    Pingfeng Fu; Qiang Zhang

    2008-01-01

    To investigate the physical and chemical properties of the steelmaking dust, wet sieve separation, XRD, SEM, EDS, and traditional chemical analysis were carried out to obtain the particle size distribution, mineralogy, morphology, and the chemical composition of the dust. The dust with a total Fe content of 64.08wt% has coarse metallic iron, magnetite and hematite grains, while fine clay minerals with a size of <38 μm are mainly iosiderite, calcium silicate, and calcite, which are conglomerated to each other.By following the procedures of wet magnetic separation, acid leaching, and oxidization calcination, magnetic materials were recycled and further prepared as iron oxide red with a productivity of 0.54 ton per unit ton of the dust. Middle iron concentrate with an Fe content of 65.92wt% can be reused as feeding material in the ironmaking industry. Additionally, washed water from acid leaching with an Fe3+ ion content of less than 5 g·L-1 was recovered as feeding water in the wet magnetic separation procedure.

  6. Interactions of proteins with biogenic iron oxyhydroxides and a new culturing technique to increase biomass yields of neutrophilic, iron-oxidizing bacteria

    OpenAIRE

    Barco, Roman A.; Edwards, Katrina J

    2014-01-01

    Neutrophilic, bacterial iron-oxidation remains one of the least understood energy-generating biological reactions to date. One of the reasons it remains under-studied is because there are inherent problems with working with iron-oxidizing bacteria (FeOB), including low biomass yields and interference from the iron oxides in the samples. In an effort to circumvent the problem of low biomass, a new large batch culturing technique was developed. Protein interactions with biogenic iron oxides wer...

  7. Oxidation of phenolic acids by soil iron and manganese oxides

    Energy Technology Data Exchange (ETDEWEB)

    Lehmann, R.G.; Cheng, H.H.; Harsh, J.B.

    Phenolic acids are intermediary metabolites of many aromatic chemicals and may be involved in humus formation, allelopathy, and nutrient availability. Depending on their structures, six phenolic acids were shown to react at different rates with oxidized forms of Fe and Mn in a Palouse soil (fine-silty, mixed, mesic Pachic Ultic Haploxeroll). Increasing methoxy substitution on the aromatic ring of phenolic acids increased the reaction rate. Reaction rate was also increased for longer carboxyl-containing side chains. After 4 h reaction, little of the applied (10 mg kg/sup -1/ soil) p-hydroxybenzoic or p-coumaric acids had reacted, while 0 to 5, 70, 90, and 100% of the vanillic, ferulic, syringic, and sinapic acids, respectively, had reacted. After 72 h under conditions limiting microbial growth, none of the p-hydroxybenzoic, 30% of the p-coumaric, and 50% of the vanillic acids had reacted. The reaction was shown to be predominantly chemical, and not biological, since phenolic acid extractabilities were similar for Palouse soil and for Palouse soil pretreated with LiOBr to remove organic matter. When the Palouse soil was pretreated with a sodium dithionite-citrate solution to remove Fe and Mn oxides, none of the phenolic acids reacted after 1 h. The reaction of sinapic acid with Palouse soil was shown to produce Fe(II) and soluble Mn as reaction products. The reaction of phenolic acids with soil was thus shown to be an oxidation of the phenolic acids, coupled with a reduction of soil Fe and Mn oxides.

  8. Evidence for Vacancy Injection during the Oxidation of Iron

    Institute of Scientific and Technical Information of China (English)

    D.G.LEES; R.FRANCIS

    2009-01-01

    Iron discs have been oxidised at 890 ℃ on one side only, with the other side protected by an inert gas. The scale-metal adhesion was very good. Initially, scale-metal adhesion was maintained by the scale relaxing towards the metal but after a time which depended upon the initial metal thickness, oxide relaxation ceased and the inert face moved towards the scale-metal interface. When the face which was normally inert was covered with a non-growing oxide layer, the scale-metal adhesion deteriorated. The results show that vacancies which were produced by oxidation were annihilated within the metal, that the inert face played a part and that the scale-metal interface is not a good sink for vacancies.

  9. Rapid Spectrophotometric Technique for Quantifying Iron in Cells Labeled with Superparamagnetic Iron Oxide Nanoparticles: Potential Translation to the Clinic

    OpenAIRE

    Dadashzadeh, Esmaeel R.; Hobson, Matthew; Bryant, L. Henry; Dean, Dana D.; Joseph A Frank

    2013-01-01

    Labeling cells with superparamagnetic iron oxide (SPIO) nanoparticles provides the ability to track cells by Magnetic Resonance Imaging. Quantifying intracellular iron concentration in SPIO labeled cells would allow for the comparison of agents and techniques used to magnetically label cells. Here we describe a rapid spectrophotometric technique (ST) to quantify iron content of SPIO labeled cells, circumventing the previous requirement of an overnight acid digestion. Following lysis with 10% ...

  10. Study of nanocomposites based on iron oxides and pectin

    Science.gov (United States)

    Chistyakova, Nataliya I.; Shapkin, Alexey A.; Sirazhdinov, Ruslan R.; Gubaidulina, Tatiana V.; Kiseleva, Tatiana Yu.; Kazakov, Alexander P.; Rusakov, Vyacheslav S.

    2014-10-01

    Mössbauer and X-ray diffraction study of nanocomposites based on iron oxides and pectin (PC) was carried out involving magnetization measurements. The concentrations of PC in nanocomposites varied from 0 to 10%. Mössbauer investigations of nanocomposites were carried out in the temperature range from 5 to 300 K. Many-state superparamagnetic relaxation model was used for spectra fitting. The magnetization, M(T,H), was measured in the temperature interval of 80-300 K and magnetic field up to 10 kOe. Formation of the "iron-polymer" interface was not observed. Particle sizes were estimated using the Mössbauer and X-ray powder diffraction data.

  11. Study of nanocomposites based on iron oxides and pectin

    Energy Technology Data Exchange (ETDEWEB)

    Chistyakova, Nataliya I., E-mail: nchistyakova@yandex.ru; Shapkin, Alexey A., E-mail: nchistyakova@yandex.ru; Sirazhdinov, Ruslan R., E-mail: nchistyakova@yandex.ru; Gubaidulina, Tatiana V., E-mail: nchistyakova@yandex.ru; Kiseleva, Tatiana Yu., E-mail: nchistyakova@yandex.ru; Kazakov, Alexander P., E-mail: nchistyakova@yandex.ru; Rusakov, Vyacheslav S., E-mail: nchistyakova@yandex.ru [M. V. Lomonosov Moscow State University, Faculty of Physics, Leninskie gory, 119991 Moscow (Russian Federation)

    2014-10-27

    Mössbauer and X-ray diffraction study of nanocomposites based on iron oxides and pectin (PC) was carried out involving magnetization measurements. The concentrations of PC in nanocomposites varied from 0 to 10%. Mössbauer investigations of nanocomposites were carried out in the temperature range from 5 to 300 K. Many-state superparamagnetic relaxation model was used for spectra fitting. The magnetization, M(T,H), was measured in the temperature interval of 80-300 K and magnetic field up to 10 kOe. Formation of the 'iron-polymer' interface was not observed. Particle sizes were estimated using the Mössbauer and X-ray powder diffraction data.

  12. RGD-conjugated iron oxide magnetic nanoparticles for magnetic resonance imaging contrast enhancement and hyperthermia.

    Science.gov (United States)

    Zheng, S W; Huang, M; Hong, R Y; Deng, S M; Cheng, L F; Gao, B; Badami, D

    2014-03-01

    The purpose of this study was to develop a specific targeting magnetic nanoparticle probe for magnetic resonance imaging and therapy in the form of local hyperthermia. Carboxymethyl dextran-coated ultrasmall superparamagnetic iron oxide nanoparticles with carboxyl groups were coupled to cyclic arginine-glycine-aspartic peptides for integrin α(v)β₃ targeting. The particle size, magnetic properties, heating effect, and stability of the arginine-glycine-aspartic-ultrasmall superparamagnetic iron oxide were measured. The arginine-glycine-aspartic-ultrasmall superparamagnetic iron oxide demonstrates excellent stability and fast magneto-temperature response. Magnetic resonance imaging signal intensity of Bcap37 cells incubated with arginine-glycine-aspartic-ultrasmall superparamagnetic iron oxide was significantly decreased compared with that incubated with plain ultrasmall superparamagnetic iron oxide. The preferential uptake of arginine-glycine-aspartic-ultrasmall superparamagnetic iron oxide by target cells was further confirmed by Prussian blue staining and confocal laser scanning microscopy.

  13. Liquid Phase Plasma Synthesis of Iron Oxide/Carbon Composite as Dielectric Material for Capacitor

    Directory of Open Access Journals (Sweden)

    Heon Lee

    2014-01-01

    Full Text Available Iron oxide/carbon composite was synthesized using a liquid phase plasma process to be used as the electrode of supercapacitor. Spherical iron oxide nanoparticles with the size of 5~10 nm were dispersed uniformly on carbon powder surface. The specific capacitance of the composite increased with increasing quantity of iron oxide precipitate on the carbon powder up to a certain quantity. When the quantity of the iron oxide precipitate exceeds the threshold, however, the specific capacitance was rather reduced by the addition of precipitate. The iron oxide/carbon composite containing an optimum quantity (0.33 atomic % of iron oxide precipitate exhibited the smallest resistance and the largest initial resistance slope.

  14. Biological iron oxidation by Gallionella spp. in drinking water production under fully aerated conditions.

    Science.gov (United States)

    de Vet, W W J M; Dinkla, I J T; Rietveld, L C; van Loosdrecht, M C M

    2011-11-01

    Iron oxidation under neutral conditions (pH 6.5-8) may be a homo- or heterogeneous chemically- or a biologically-mediated process. The chemical oxidation is supposed to outpace the biological process under slightly alkaline conditions (pH 7-8). The iron oxidation kinetics and growth of Gallionella spp. - obligatory chemolithotrophic iron oxidizers - were assessed in natural, organic carbon-containing water, in continuous lab-scale reactors and full-scale groundwater trickling filters in the Netherlands. From Gallionella cell numbers determined by qPCR, balances were made for all systems. The homogeneous chemical iron oxidation occurred in accordance with the literature, but was retarded by a low water temperature (13 °C). The contribution of the heterogeneous chemical oxidation was, despite the presence of freshly formed iron oxyhydroxides, much lower than in previous studies in ultrapure water. This could be caused by the adsorption of natural organic matter (NOM) on the iron oxide surfaces. In the oxygen-saturated natural water with a pH ranging from 6.5 to 7.7, Gallionella spp. grew uninhibited and biological iron oxidation was an important, and probably the dominant, process. Gallionella growth was not even inhibited in a full-scale filter after plate aeration. From this we conclude that Gallionella spp. can grow under neutral pH and fully aerated conditions when the chemical iron oxidation is retarded by low water temperature and inhibition of the autocatalytic iron oxidation.

  15. Chitosan-Iron Oxide Coated Graphene Oxide Nanocomposite Hydrogel: A Robust and Soft Antimicrobial Biofilm.

    Science.gov (United States)

    Konwar, Achyut; Kalita, Sanjeeb; Kotoky, Jibon; Chowdhury, Devasish

    2016-08-17

    We report a robust biofilm with antimicrobial properties fabricated from chitosan-iron oxide coated graphene oxide nanocomposite hydrogel. For the first time, the coprecipitation method was used for the successful synthesis of iron oxide coated graphene oxide (GIO) nanomaterial. After this, films were fabricated by the gel-casting technique aided by the self-healing ability of the chitosan hydrogel network system. Both the nanomaterial and the nanocomposite films were characterized by techniques such as scanning electron microscopy, FT-IR spectroscopy, X-ray diffraction, and vibrating sample magnetometry. Measurements of the thermodynamic stability and mechanical properties of the films indictaed a significant improvement in their thermal and mechanical properties. Moreover, the stress-strain profile indicated the tough nature of the nanocomposite hydrogel films. These improvements, therefore, indicated an effective interaction and good compatibility of the GIO nanomaterial with the chitosan hydrogel matrix. In addition, it was also possible to fabricate films with tunable surface properties such as hydrophobicity simply by varying the loading percentage of GIO nanomaterial in the hydrogel matrix. Fascinatingly, the chitosan-iron oxide coated graphene oxide nanocomposite hydrogel films displayed significant antimicrobial activities against both Gram-positive and Gram-negative bacterial strains, such as methicillin-resistant Staphylococcus aureus, Staphylococcus aureus, and Escherichia coli, and also against the opportunistic dermatophyte Candida albicans. The antimicrobial activities of the films were tested by agar diffusion assay and antimicrobial testing based on direct contact. A comparison of the antimicrobial activity of the chitosan-GIO nanocomposite hydrogel films with those of individual chitosan-graphene oxide and chitosan-iron oxide nanocomposite films demonstrated a higher antimicrobial activity for the former in both types of tests. In vitro hemolysis

  16. A new method for preparation of magnetite from iron oxyhydroxide or iron oxide and ferrous salt in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Kahani, S.A. [Department of Chemistry, Faculty of Science, University of Kashan, Kashan 87317-51167 (Iran, Islamic Republic of)], E-mail: Kahani@kashanu.ac.ir; Jafari, M. [Department of Chemistry, Faculty of Science, University of Kashan, Kashan 87317-51167 (Iran, Islamic Republic of)

    2009-07-15

    In this study, a new method is proposed for the preparation of Fe{sub 3}O{sub 4} from iron oxyhydroxides (goethite, akaganeite, lepidocrocite, feroxyhyte and ferrihydrite) or iron oxide (hematite) and ferrous salt in aqueous solution. The product is magnetite with various particle sizes. Products are characterized by X-ray powder diffraction, IR spectra and vibrating sample magnetometery.

  17. Aqueous dispersion of monodisperse magnetic iron oxide nanocrystals through phase transfer

    Energy Technology Data Exchange (ETDEWEB)

    Yu, William W [Department of Chemistry, Rice University, Houston, TX 77005 (United States); Chang, Emmanuel [Department of Bioengineering, Rice University, Houston, TX 77005 (United States); Sayes, Christie M [Department of Chemistry, Rice University, Houston, TX 77005 (United States); Drezek, Rebekah [Department of Bioengineering, Rice University, Houston, TX 77005 (United States); Colvin, Vicki L [Department of Chemistry, Rice University, Houston, TX 77005 (United States)

    2006-09-14

    A facile method was developed for completely transferring high quality monodisperse iron oxide nanocrystals from organic solvents to water. The as-prepared aqueous dispersions of iron oxide nanocrystals were extremely stable and could be functionalized for bioconjugation with biomolecules. These iron oxide nanocrystals showed negligible cytotoxicity to human breast cancer cells (SK-BR-3) and human dermal fibroblast cells. This method is general and versatile for many organic solvent-synthesized nanoparticles, including fluorescent semiconductor nanocrystals.

  18. Iron oxide-based nanomagnets in nanomedicine: fabrication and applications

    Directory of Open Access Journals (Sweden)

    Meng Meng Lin

    2010-02-01

    Full Text Available Iron oxide-based nanomagnets have attracted a great deal of attention in nanomedicine over the past decade. Down to the nanoscale, superparamagnetic iron oxide nanoparticles can only be magnetized in the presence of an external magnetic field, which makes them capable of forming stable colloids in a physio-biological medium. Their superparamagnetic property, together with other intrinsic properties, such as low cytotoxicity, colloidal stability, and bioactive molecule conjugation capability, makes such nanomagnets ideal in both in-vitro and in-vivo biomedical applications. In this review, a chemical, physical, and biological synthetic approach to prepare iron oxide-based nanomagnets with different physicochemical properties was illustrated and compared. The growing interest in iron oxide-based nanomagnets with multifunctionalities was explored in cancer diagnostics and treatment, focusing on their combined roles in a magnetic resonance contrast agent, hyperthermia, and magnetic force assisted drug delivery. Iron oxides as magnetic carriers in gene therapy were reviewed with a focus on the sophisticated design and construction of magnetic vectors. Finally, the iron oxide-based nanomagnet also represents a very promising tool in particle/cell interfacing in controlling cellular functionalities, such as adhesion, proliferation, differentiation, and cell patterning, in stem cell therapy and tissue engineering applications. Meng Meng Lin received a BSc in biotechnology at the University of Hong Kong, China in 2004 and an MSc in biomedical nanotechnology at Newcastle University, UK, in 2005. She is currently working toward her PhD at the Institute of Science and Technology in Medicine, Keele University, UK. She was a visiting student at the Royal Institute of Technology, Sweden, in 2006. Her research interests include nanoparticles preparation, cell/nanomaterials interface, and cancer-oriented drug delivery. Hyung-Hwan Kim received an MSc degree in

  19. Synthesis of iron oxide nanoparticles via sonochemical method and their characterization

    Institute of Scientific and Technical Information of China (English)

    Amir Hassanjani-Roshan; Mohammad Reza Vaezi; Ali Shokuhfar; Zohreh Rajabali

    2011-01-01

    Preparation of iron oxide (α-Fe2O3) nanoparticles was carried out via a sonochemical process. The process parameters such as temperature,sonication time and power of ultrasonication play important roles in the size and morphology of the final products. The iron oxide nanoparticles were characterized by transmission electron microscopy,X-ray powder diffraction,and thermogravimetric and differential thermal analyses. From transmission electron microscopy observations,the size of the iron oxide nanoparticles is estimated to be significantly smaller than 19 nm. X-ray diffraction data of the powder after annealing provide direct evidence that the iron oxide was formed during the sonochemical process.

  20. Iron: the Redox-active center of oxidative stress in Alzheimer disease.

    Science.gov (United States)

    Castellani, Rudy J; Moreira, Paula I; Liu, Gang; Dobson, Jon; Perry, George; Smith, Mark A; Zhu, Xiongwei

    2007-10-01

    Although iron is essential in maintaining the function of the central nervous system, it is a potent source of reactive oxygen species. Excessive iron accumulation occurs in many neurodegenerative diseases including Alzheimer disease (AD), Parkinson's disease, and Creutzfeldt-Jakob disease, raising the possibility that oxidative stress is intimately involved in the neurodegenerative process. AD in particular is associated with accumulation of numerous markers of oxidative stress; moreover, oxidative stress has been shown to precede hallmark neuropathological lesions early in the disease process, and such lesions, once present, further accumulate iron, among other markers of oxidative stress. In this review, we discuss the role of iron in the progression of AD.

  1. Enriched iron(III-reducing bacterial communities are shaped by carbon substrate and iron oxide mineralogy

    Directory of Open Access Journals (Sweden)

    Christopher J. Lentini

    2012-12-01

    Full Text Available Iron (Fe oxides exist in a spectrum of structures in the environment, with ferrihydrite widely considered the most bioavailable phase. Yet, ferrihydrite is unstable and rapidly transforms to more crystalline Fe(III oxides (e.g., goethite, hematite, which are poorly reduced by model dissimilatory Fe(III-reducing microorganisms. This begs the question, what processes and microbial groups are responsible for reduction of crystalline Fe(III oxides within sedimentary environments? Further, how do changes in Fe mineralogy shape oxide-hosted microbial populations? To address these questions, we conducted a large-scale cultivation effort using various Fe(III oxides (ferrihydrite, goethite, hematite and carbon substrates (glucose, lactate, acetate along a dilution gradient to enrich for microbial populations capable of reducing Fe oxides spanning a wide range of crystallinities and reduction potentials. While carbon source was the most important variable shaping community composition within Fe(III-reducing enrichments, both Fe oxide type and sediment dilution also had a substantial influence. For instance, with acetate as the carbon source, only ferrihydrite enrichments displayed a significant amount of Fe(III reduction and the well known dissimilatory metal reducer Geobacter sp. was the dominant organism enriched. In contrast, when glucose and lactate were provided, all three Fe oxides were reduced and reduction coincided with the presence of fermentative (e.g. Enterobacter spp. and sulfate-reducing bacteria (e.g. Desulfovibrio spp.. Thus, changes in Fe oxide structure and resource availability may shift Fe(III-reducing communities between dominantly metal-respiring to fermenting and/or sulfate-reducing organisms which are capable of reducing more recalcitrant Fe phases. These findings highlight the need for further targeted investigations into the composition and activity of speciation-directed metal-reducing populations within natural environments.

  2. Synthesis and Characterization of Holmium-Doped Iron Oxide Nanoparticles

    Directory of Open Access Journals (Sweden)

    Maarten Bloemen

    2014-02-01

    Full Text Available Rare earth atoms exhibit several interesting properties, for example, large magnetic moments and luminescence. Introducing these atoms into a different matrix can lead to a material that shows multiple interesting effects. Holmium atoms were incorporated into an iron oxide nanoparticle and the concentration of the dopant atom was changed in order to determine its influence on the host crystal. Its magnetic and magneto-optical properties were investigated by vibrating sample magnetometry and Faraday rotation measurements. The luminescent characteristics of the material, in solution and incorporated in a polymer thin film, were probed by fluorescence experiments.

  3. Catalytic effect of free iron ions and heme-iron on chromophore oxidation of a polyene antibiotic amphotericin B

    Science.gov (United States)

    Czernel, Grzegorz; Typek, Rafał; Klimek, Katarzyna; Czuryło, Aleksandra; Dawidowicz, Andrzej L.; Gagoś, Mariusz

    2016-05-01

    Owing to the presence of a chromophore in the amphotericin B (AmB) structure, the molecule can undergo the oxidation process. In this research, AmB chromophore oxidation was catalysed by iron ions (iron(III) chloride (FeCl3), pH 2.5) and by heme-iron (methemoglobin (HbFe(III)), and hemin (heme-Fe(III)) at pH 7.0). Additionally, we compared oxidation processes induced by the aforementioned oxidizing agents with autoxidation by dioxygen (O2) naturally occurring in a sample. The effects of the interaction of the oxidizing agents with AmB were analysed using molecular spectroscopies (electronic absorption (UV-Vis), fluorescence) and LC-MS. The use of a 1,10-phenanthroline (phen) chelator facilitated unambiguous determination of the oxidative effect of free iron(III) ions (FeIII) in an acidic solution on the AmB molecules. Also, the changes in the spectra of fluorescence emission centred at ∼470 nm indicate iron-catalysed processes of AmB chromophore oxidation. Unexpectedly, we found a similar spectroscopic effect for AmB induced by methemoglobin and hemin at pH 7.0. Methemoglobin and hemin at a concentration of 8 × 10-7 M (physiological) significantly increases the rate of the processes of AmB chromophore oxidation relative to the process of autoxidation.

  4. Thermo-electric oxidization of iron in lithium niobate crystals

    Energy Technology Data Exchange (ETDEWEB)

    Falk, Matthias

    2007-07-01

    Lithium niobate crystals (LiNbO{sub 3}) are a promising material for nonlinear-optical applications like frequency conversion to generate visible light, e.g., in laser displays, but their achievable output power is greatly limited by the ''optical damage'', i.e., light-induced refractive-index changes caused by excitation of electrons from iron impurities and the subsequent retrapping in unilluminated areas of the crystal. The resulting space-charge fields modify the refractive indices due to the electro-optic effect. By this ''photorefractive effect'' the phase-matching condition, i.e., the avoidance of destructive interference between light generated at different crystal positions due to the dispersion of the fundamental wave and the converted wave, is disturbed critically above a certain light intensity threshold. The influence of annealing treatments conducted in the presence of an externally applied electric field (''thermo-electric oxidization'') on the valence state of iron impurities and thereby on the optical damage is investigated. It is observed that for highly iron-doped LiNbO{sub 3} crystals this treatment leads to a nearly complete oxidization from Fe{sup 2+} to Fe{sup 3+} indicated by the disappearance of the absorption caused by Fe{sup 2+}. During the treatment an absorption front forms that moves through the crystal. The absorption in the visible as well as the electrical conductivity are decreased by up to five orders of magnitude due to this novel treatment. The ratio of the Fe{sup 2+} concentration to the total iron concentration - a measure for the strength of the oxidization - is in the order of 10{sup -6} for oxidized crystals whereas it is about 10{sup -1} for untreated samples. Birefringence changes are observed at the absorption front that are explained by the removal of hydrogen and lithium ions from the crystal that compensate for the charges of the also removed electrons from

  5. Reactions of metal ions at surfaces of hydrous iron oxide

    Science.gov (United States)

    Hem, J.D.

    1977-01-01

    Cu, Ag and Cr concentrations in natural water may be lowered by mild chemical reduction involving ferric hydroxide-ferrous ion redox processes. V and Mo solubilities may be controlled by precipitation of ferrous vanadate or molybdate. Concentrations as low as 10-8.00 or 10-9.00 M are readily attainable for all these metals in oxygen-depleted systems that are relatively rich in Fe. Deposition of manganese oxides such as Mn3O4 can be catalyzed in oxygenated water by coupling to ferrous-ferric redox reactions. Once formed, these oxides may disproportionate, giving Mn4+ oxides. This reaction produces strongly oxidizing conditions at manganese oxide surfaces. The solubility of As is significantly influenced by ferric iron only at low pH. Spinel structures such as chromite or ferrites of Cu, Ni, and Zn, are very stable and if locally developed on ferric hydroxide surfaces could bring about solubilities much below 10-9.00 M for divalent metals near neutral pH. Solubilities calculated from thermodynamic data are shown graphically and compared with observed concentrations in some natural systems. ?? 1977.

  6. Molecular modeling studies of oleate adsorption on iron oxides

    Energy Technology Data Exchange (ETDEWEB)

    Rath, Swagat S. [CSIR-Institute of Minerals and Materials Technology, Bhubaneswar (India); Sinha, Nishant [Accelrys K.K, Bengaluru (India); Sahoo, Hrushikesh [CSIR-Institute of Minerals and Materials Technology, Bhubaneswar (India); Das, Bisweswar, E-mail: bdas@immt.res.in [CSIR-Institute of Minerals and Materials Technology, Bhubaneswar (India); Mishra, Barada Kanta [CSIR-Institute of Minerals and Materials Technology, Bhubaneswar (India)

    2014-03-01

    Graphical abstract: - Highlights: • Plane wave periodic DFT study of oleate-iron oxide interaction. • Magnetite-oleate complex is more stable than hematite and goethite. • Flotation recovery of magnetite is more compared to the other two oxides. - Abstract: Comparative studies of oleate interaction with hematite, magnetite and goethite using density functional calculations are presented. The approach is illustrated by carrying out geometric optimization of oleate on the stable and most exposed planes of hematite, magnetite, and goethite. Interaction energies for oleate-mineral surface have been determined, based on which, magnetite is found to be forming the most stable complex with oleate. Trend as obtained from the quantum chemical calculations has been validated by contact angle measurements and flotation studies on hematite, magnetite and goethite with sodium oleate at different pH and collector concentrations.

  7. Iron and oxygen isotope fractionation during iron UV photo-oxidation: Implications for early Earth and Mars

    Science.gov (United States)

    Nie, Nicole X.; Dauphas, Nicolas; Greenwood, Richard C.

    2017-01-01

    Banded iron formations (BIFs) contain appreciable amounts of ferric iron (Fe3+). The mechanism by which ferrous iron (Fe2+) was oxidized into Fe3+ in an atmosphere that was globally anoxic is highly debated. Of the three scenarios that have been proposed to explain BIF formation, photo-oxidation by UV photons is the only one that does not involve life (the other two are oxidation by O2 produced by photosynthesis, and anoxygenic photosynthesis whereby Fe2+ is directly used as electron donor in place of water). We experimentally investigated iron and oxygen isotope fractionation imparted by iron photo-oxidation at a pH of 7.3. The iron isotope fractionation between precipitated Fe3+-bearing lepidocrocite and dissolved Fe2+ follows a Rayleigh distillation with an instantaneous 56Fe/54Fe fractionation factor of + 1.2 ‰. Such enrichment in the heavy isotopes of iron is consistent with the values measured in BIFs. We also investigated the nature of the mass-fractionation law that governs iron isotope fractionation in the photo-oxidation experiments (i.e., the slope of the δ56Fe-δ57Fe relationship). The experimental run products follow a mass-dependent law corresponding to the high-T equilibrium limit. The fact that a ∼3.8 Gyr old BIF sample (IF-G) from Isua (Greenland) falls on the same fractionation line confirms that iron photo-oxidation in the surface layers of the oceans was a viable pathway to BIF formation in the Archean, when the atmosphere was largely transparent to UV photons. Our experiments allow us to estimate the quantum yield of the photo-oxidation process (∼0.07 iron atom oxidized per photon absorbed). This yield is used to model iron oxidation on early Mars. As the photo-oxidation proceeds, the aqueous medium becomes more acidic, which slows down the reaction by changing the speciation of iron to species that are less efficient at absorbing UV-photons. Iron photo-oxidation in centimeter to meter-deep water ponds would take months to years to

  8. Homogeneous, heterogeneous and biological oxidation of iron(II) in rapid sand filtration

    NARCIS (Netherlands)

    Beek, van C.G.E.M.; Hiemstra, T.; Hofs, B.; Nederlof, M.M.; Paassen, van J.A.M.; Reijnen, G.K.

    2012-01-01

    Homogeneous, heterogeneous and biological oxidation may precipitate iron(II) as iron(III) hydroxides. In this paper we evaluate the conditions under which each of these processes is dominant in rapid sand filtration (RSF). It is demonstrated that in the presence of iron(III) hydroxide precipitates h

  9. Targeted magnetic iron oxide nanoparticles for tumor imaging and therapy

    Directory of Open Access Journals (Sweden)

    Xiang-Hong Peng

    2008-10-01

    Full Text Available Xiang-Hong Peng1,4, Ximei Qian2,4, Hui Mao3,4, Andrew Y Wang5, Zhuo (Georgia Chen1,4, Shuming Nie2,4, Dong M Shin1,4*1Department of Medical Oncology/Hematology; 2Department of Biomedical Engineering; 3Department of Radiology; 4Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA; 5Ocean Nanotech, LLC, Fayetteville, AR, USAAbstract: Magnetic iron oxide (IO nanoparticles with a long blood retention time, biodegradability and low toxicity have emerged as one of the primary nanomaterials for biomedical applications in vitro and in vivo. IO nanoparticles have a large surface area and can be engineered to provide a large number of functional groups for cross-linking to tumor-targeting ligands such as monoclonal antibodies, peptides, or small molecules for diagnostic imaging or delivery of therapeutic agents. IO nanoparticles possess unique paramagnetic properties, which generate significant susceptibility effects resulting in strong T2 and T*2 contrast, as well as T1 effects at very low concentrations for magnetic resonance imaging (MRI, which is widely used for clinical oncology imaging. We review recent advances in the development of targeted IO nanoparticles for tumor imaging and therapy.Keywords: iron oxide nanoparticles, tumor imaging, MRI, therapy

  10. Thermal and magnetic properties of chitosan-iron oxide nanoparticles.

    Science.gov (United States)

    Soares, Paula I P; Machado, Diana; Laia, César; Pereira, Laura C J; Coutinho, Joana T; Ferreira, Isabel M M; Novo, Carlos M M; Borges, João Paulo

    2016-09-20

    Chitosan is a biopolymer widely used for biomedical applications such as drug delivery systems, wound healing, and tissue engineering. Chitosan can be used as coating for other types of materials such as iron oxide nanoparticles, improving its biocompatibility while extending its range of applications. In this work iron oxide nanoparticles (Fe3O4 NPs) produced by chemical precipitation and thermal decomposition and coated with chitosan with different molecular weights were studied. Basic characterization on bare and chitosan-Fe3O4 NPs was performed demonstrating that chitosan does not affect the crystallinity, chemical composition, and superparamagnetic properties of the Fe3O4 NPs, and also the incorporation of Fe3O4 NPs into chitosan nanoparticles increases the later hydrodynamic diameter without compromising its physical and chemical properties. The nano-composite was tested for magnetic hyperthermia by applying an alternating current magnetic field to the samples demonstrating that the heating ability of the Fe3O4 NPs was not significantly affected by chitosan.

  11. Application of a novel plasma-induced CD/MWCNT/iron oxide composite in zinc decontamination.

    Science.gov (United States)

    Yang, Shitong; Guo, Zhiqiang; Sheng, Guodong; Wang, Xiangke

    2012-10-01

    Herein, β-cyclodextrin (β-CD) was grafted onto magnetic MWCNT/iron oxide particles by using low temperature plasma-induced technique to synthesize a novel nanocomposite. The prepared composite (denoted as CD/MWCNT/iron oxide) exhibited high magnetic property (saturation magnetization M(s)=37.8 emu/g) and good dispersion property in aqueous solution. Batch experiments were conducted to evaluate the application potential of CD/MWCNT/iron oxide in the decontamination of Zn(II) from aqueous solutions. The sorption amount of Zn(II) on CD/MWCNT/iron oxide was higher than that of Zn(II) on MWCNT/iron oxides and oxidized MWCNTs, indicating that the grafted β-CD could enhance the sorption capacity of CD/MWCNT/iron oxide composite toward Zn(II) by providing multiple hydroxyl functional groups. Due to its high magnetic, CD/MWCNT/iron oxide could be easily separated from aqueous solution with an external magnetic field. Regeneration studies suggested that CD/MWCNT/iron oxide can support long term use as a cost-effective material in sewage treatment with minimum replacement costs.

  12. Mapping the Iron Oxidation State in Martian Meteorites

    Science.gov (United States)

    Martin, A. M.; Treimann, A. H.; Righter, K.

    2017-01-01

    Several types of Martian igneous meteorites have been identified: clinopyroxenites (nakhlites), basaltic shergottites, peridotitic shergottites, dunites (chassignites) and orthopyroxenites [1,2]. In order to constrain the heterogeneity of the Martian mantle and crust, and their evolution through time, numerous studies have been performed on the iron oxidation state of these meteorites [3,4,5,6,7,8,9]. The calculated fO2 values all lie within the FMQ-5 to FMQ+0.5 range (FMQ representing the Fayalite = Magnetite + Quartz buffer); however, discrepancies appear between the various studies, which are either attributed to the choice of the minerals/melts used, or to the precision of the analytical/calculation method. The redox record in volcanic samples is primarily related to the oxidation state in the mantle source(s). However, it is also influenced by several deep processes: melting, crystallization, magma mixing [10], assimilation and degassing [11]. In addition, the oxidation state in Martian meteorites is potentially affected by several surface processes: assimilation of sediment/ crust during lava flowing at Mars' surface, low temperature micro-crystallization [10], weathering at the surface of Mars and low temperature reequilibration, impact processes (i.e. high pressure phase transitions, mechanical mixing, shock degassing and melting), space weathering, and weathering on Earth (at atmospheric conditions different from Mars). Decoding the redox record of Martian meteorites, therefore, requires large-scale quantitative analysis methods, as well as a perfect understanding of oxidation processes.

  13. Atomistic Simulations of Uranium Incorporation into Iron (Hydr)Oxides

    Energy Technology Data Exchange (ETDEWEB)

    Kerisit, Sebastien N.; Felmy, Andrew R.; Ilton, Eugene S.

    2011-04-29

    Atomistic simulations were carried out to characterize the coordination environments of U incorporated in three Fe-(hydr)oxide minerals: goethite, magnetite, and hematite. The simulations provided information on U-O and U-Fe distances, coordination numbers, and lattice distortion for U incorporated in different sites (e.g., unoccupied versus occupied sites, octahedral versus tetrahedral) as a function of the oxidation state of U and charge compensation mechanisms (i.e., deprotonation, vacancy formation, or reduction of Fe(III) to Fe(II)). For goethite, deprotonation of first shell hydroxyls enables substitution of U for Fe(III) with a minimal amount of lattice distortion, whereas substitution in unoccupied octahedral sites induced appreciable distortion to 7-fold coordination regardless of U oxidation states and charge compensation mechanisms. Importantly, U-Fe distances of ~3.6 Å were associated with structural incorporation of U and cannot be considered diagnostic of simple adsorption to goethite surfaces. For magnetite, the octahedral site accommodates U(V) or U(VI) with little lattice distortion. U substituted for Fe(III) in hematite maintained octahedral coordination in most cases. In general, comparison of the simulations with available experimental data provides further evidence for the structural incorporation of U in iron (hydr)oxide minerals.

  14. Iron isotope fractionation during microbial dissimilatory iron oxide reduction in simulated Archaean seawater.

    Science.gov (United States)

    Percak-Dennett, E M; Beard, B L; Xu, H; Konishi, H; Johnson, C M; Roden, E E

    2011-05-01

    The largest Fe isotope excursion yet measured in marine sedimentary rocks occurs in shales, carbonates, and banded iron formations of Neoarchaean and Paleoproterozoic age. The results of field and laboratory studies suggest a potential role for microbial dissimilatory iron reduction (DIR) in producing this excursion. However, most experimental studies of Fe isotope fractionation during DIR have been conducted in simple geochemical systems, using pure Fe(III) oxide substrates that are not direct analogues to phases likely to have been present in Precambrian marine environments. In this study, Fe isotope fractionation was investigated during microbial reduction of an amorphous Fe(III) oxide-silica coprecipitate in anoxic, high-silica, low-sulphate artificial Archaean seawater at 30 °C to determine if such conditions alter the extent of reduction or isotopic fractionations relative to those observed in simple systems. The Fe(III)-Si coprecipitate was highly reducible (c. 80% reduction) in the presence of excess acetate. The coprecipitate did not undergo phase conversion (e.g. to green rust, magnetite or siderite) during reduction. Iron isotope fractionations suggest that rapid and near-complete isotope exchange took place among all Fe(II) and Fe(III) components, in contrast to previous work on goethite and hematite, where exchange was limited to the outer few atom layers of the substrate. Large quantities of low-δ(56)Fe Fe(II) (aqueous and solid phase) were produced during reduction of the Fe(III)-Si coprecipitate. These findings shed new light on DIR as a mechanism for producing Fe isotope variations observed in Neoarchaean and Paleoproterozoic marine sedimentary rocks.

  15. The role of iron as a mediator of oxidative stress in Alzheimer disease.

    Science.gov (United States)

    Castellani, Rudy J; Moreira, Paula I; Perry, George; Zhu, Xiongwei

    2012-01-01

    Iron is both essential for maintaining a spectrum of metabolic processes in the central nervous system and elsewhere, and potent source of reactive oxygen species. Redox balance with respect to iron, therefore, may be critical to human neurodegenerative disease but is also in need of better understanding. Alzheimer disease (AD) in particular is associated with accumulation of numerous markers of oxidative stress; moreover, oxidative stress has been shown to precede hallmark neuropathological lesions early in the disease process, and such lesions, once present, further accumulate iron, among other markers of oxidative stress. In this review, we discuss the role of iron in the progression of AD.

  16. [Neutrophilic lithotrophic iron-oxidizing prokaryotes and their role in the biogeochemical processes of the iron cycle].

    Science.gov (United States)

    2014-01-01

    Biology of lithotrophic neutrophilic iron-oxidizing prokaryotes and their role in the processes of the biogeochemical cycle of iron are discussed. This group of microorganisms is phylogenetically, taxonomically, and physiologically heterogeneous, comprising three metabolically different groups: aerobes, nitrate-dependent anaerobes, and phototrophs; the latter two groups have been revealed relatively recently. Their taxonomy and metabolism are described. Materials on the structure and functioning of the electron transport chain in the course of Fe(II) oxidation by members of various physiological groups are discussed. Occurrence of iron oxidizers in freshwater and marine ecosystems, thermal springs, areas of hydrothermal activity, and underwater volcanic areas are considered. Molecular genetic techniques were used to determine the structure of iron-oxidizing microbial communities in various natural ecosystems. Analysis of stable isotope fractioning of 56/54Fe in pure cultures and model experiments revealed predominance of biological oxidation over abiotic ones in shallow aquatic habitats and mineral springs, which was especially pronounced under microaerobic conditions at the redox zone boundary. Discovery of anaerobic bacterial Fe(II) oxidation resulted in development of new hypotheses concerning the possible role of microorganisms and the mechanisms of formation of the major iron ore deposits in Precambrian and early Proterozoic epoch. Paleobiological data are presented on the microfossils and specific biomarkers retrieved from ancient ore samples and confirming involvement of anaerobic biogenic processes in their formation.

  17. Oxygen vacancy promoted methane partial oxidation over iron oxide oxygen carriers in the chemical looping process.

    Science.gov (United States)

    Cheng, Zhuo; Qin, Lang; Guo, Mengqing; Xu, Mingyuan; Fan, Jonathan A; Fan, Liang-Shih

    2016-11-30

    We perform ab initio DFT+U calculations and experimental studies of the partial oxidation of methane to syngas on iron oxide oxygen carriers to elucidate the role of oxygen vacancies in oxygen carrier reactivity. In particular, we explore the effect of oxygen vacancy concentration on sequential processes of methane dehydrogenation, and oxidation with lattice oxygen. We find that when CH4 adsorbs onto Fe atop sites without neighboring oxygen vacancies, it dehydrogenates with CHx radicals remaining on the same site and evolves into CO2via the complete oxidation pathway. In the presence of oxygen vacancies, on the other hand, the formed methyl (CH3) prefers to migrate onto the vacancy site while the H from CH4 dehydrogenation remains on the original Fe atop site, and evolves into CO via the partial oxidation pathway. The oxygen vacancies created in the oxidation process can be healed by lattice oxygen diffusion from the subsurface to the surface vacancy sites, and it is found that the outward diffusion of lattice oxygen atoms is more favorable than the horizontal diffusion on the same layer. Based on the proposed mechanism and energy profile, we identify the rate-limiting steps of the partial oxidation and complete oxidation pathways. Also, we find that increasing the oxygen vacancy concentration not only lowers the barriers of CH4 dehydrogenation but also the cleavage energy of Fe-C bonds. However, the barrier of the rate-limiting step cannot further decrease when the oxygen vacancy concentration reaches 2.5%. The fundamental insight into the oxygen vacancy effect on CH4 oxidation with iron oxide oxygen carriers can help guide the design and development of more efficient oxygen carriers and CLPO processes.

  18. Identification of Iron Oxides Qualitatively/Quantitatively Formed during the High Temperature Oxidation of Superalloys in Air and Steam Environments

    Institute of Scientific and Technical Information of China (English)

    M.Siddique; N.Hussain; M.Shafi

    2009-01-01

    Mossbauer spectroscopy has been used to study the morphology of iron oxides formed during the oxidation of superalloys, such as SS-304L (1.4306S), Incoloy-800H, Incoloy-825, UBHA-25L, Sanicro-28 and Inconel-690, at 1200℃ exposed in air and steam environments for 400 h. The basic aim was to identify and compare the iron oxides qualitatively and quantitatively, formed during the oxidation of these alloys in two environments. The behaviour of alloy UBHA-25L in high temperature oxidation in both environments indicates that it has good oxidation resistance especially in steam, whereas Sanicro-28 has excellent corrosion resistance in steam environment. In air oxidation of lnconel-690 no iron oxide, with established Mossbauer parameters, was detected.

  19. Iron-oxide minerals affect extracellular electron-transfer paths of Geobacter spp.

    Science.gov (United States)

    Kato, Souichiro; Hashimoto, Kazuhito; Watanabe, Kazuya

    2013-01-01

    Some bacteria utilize (semi)conductive iron-oxide minerals as conduits for extracellular electron transfer (EET) to distant, insoluble electron acceptors. A previous study demonstrated that microbe/mineral conductive networks are constructed in soil ecosystems, in which Geobacter spp. share dominant populations. In order to examine how (semi)conductive iron-oxide minerals affect EET paths of Geobacter spp., the present study grew five representative Geobacter strains on electrodes as the sole electron acceptors in the absence or presence of (semi)conductive iron oxides. It was found that iron-oxide minerals enhanced current generation by three Geobacter strains, while no effect was observed in another strain. Geobacter sulfurreducens was the only strain that generated substantial amounts of currents both in the presence and absence of the iron oxides. Microscopic, electrochemical and transcriptomic analyses of G. sulfurreducens disclosed that this strain constructed two distinct types of EET path; in the absence of iron-oxide minerals, bacterial biofilms rich in extracellular polymeric substances were constructed, while composite networks made of mineral particles and microbial cells (without polymeric substances) were developed in the presence of iron oxides. It was also found that uncharacterized c-type cytochromes were up-regulated in the presence of iron oxides that were different from those found in conductive biofilms. These results suggest the possibility that natural (semi)conductive minerals confer energetic and ecological advantages on Geobacter, facilitating their growth and survival in the natural environment.

  20. Magnetic and Mössbauer spectroscopy studies of nanocrystalline iron oxide aerogels

    DEFF Research Database (Denmark)

    Carpenter, E.E.; Long, J.W.; Rolison, D.R.

    2006-01-01

    A sol-gel synthesis was used to produce iron oxide aerogels. These nanocrystalline aerogels have a pore-solid structure similar to silica aerogels but are composed entirely of iron oxides. Mössbauer experiments and x-ray diffraction showed that the as-prepared aerogel is an amorphous or poorly...

  1. HREM investigation of the constitution and the crystallography of thin thermal oxide layers on iron

    DEFF Research Database (Denmark)

    Graat, P.C.J.; Brongers, M.P.H.; Zandbergen, H.W.

    1997-01-01

    Oxide layers formed at 573 K in O2 at atmospheric pressure, both on a clean iron surface and on an iron surface covered with an etching induced (hydro)oxide film, were investigated with high-resolution transmission electron microscopy (HREM). Cross-sections of oxidised samples were prepared by a ...

  2. Cell adhesion of Shewanella oneidensis to iron oxide minerals: Effect of different single crystal faces

    OpenAIRE

    Hochella Michael F; Bank Tracy L; Neal Andrew L; Rosso Kevin M

    2005-01-01

    The results of experiments designed to test the hypothesis that near-surface molecular structure of iron oxide minerals influences adhesion of dissimilatory iron reducing bacteria are presented. These experiments involved the measurement, using atomic force microscopy, of interaction forces generated between Shewanella oneidensis MR-1 cells and single crystal growth faces of iron oxide minerals. Significantly different adhesive force was measured between cells and the (001) face of hematite,...

  3. Iron binding at specific sites within the octameric HbpS protects streptomycetes from iron-mediated oxidative stress.

    Directory of Open Access Journals (Sweden)

    Ina Wedderhoff

    Full Text Available The soil bacterium Streptomyces reticuli secretes the octameric protein HbpS that acts as a sensory component of the redox-signalling pathway HbpS-SenS-SenR. This system modulates a genetic response on iron- and haem-mediated oxidative stress. Moreover, HbpS alone provides this bacterium with a defence mechanism to the presence of high concentrations of iron ions and haem. While the protection against haem has been related to its haem-binding and haem-degrading activity, the interaction with iron has not been studied in detail. In this work, we biochemically analyzed the iron-binding activity of a set of generated HbpS mutant proteins and present evidence showing the involvement of one internal and two exposed D/EXXE motifs in binding of high quantities of ferrous iron, with the internal E78XXE81 displaying the tightest binding. We additionally show that HbpS is able to oxidize ferrous to ferric iron ions. Based on the crystal structure of both the wild-type and the mutant HbpS-D78XXD81, we conclude that the local arrangement of the side chains from the glutamates in E78XXE81 within the octameric assembly is a pre-requisite for interaction with iron. The data obtained led us to propose that the exposed and the internal motif build a highly specific route that is involved in the transport of high quantities of iron ions into the core of the HbpS octamer. Furthermore, physiological studies using Streptomyces transformants secreting either wild-type or HbpS mutant proteins and different redox-cycling compounds led us to conclude that the iron-sequestering activity of HbpS protects these soil bacteria from the hazardous side effects of peroxide- and iron-based oxidative stress.

  4. Designed synthesis and surface engineering strategies of magnetic iron oxide nanoparticles for biomedical applications.

    Science.gov (United States)

    Wu, Wei; Jiang, Chang Zhong; Roy, Vellaisamy A L

    2016-12-01

    Iron oxide nanoparticles (NPs) hold great promise for future biomedical applications because of their magnetic properties as well as other intrinsic properties such as low toxicity, colloidal stability, and surface engineering capability. Numerous related studies on iron oxide NPs have been conducted. Recent progress in nanochemistry has enabled fine control over the size, crystallinity, uniformity, and surface properties of iron oxide NPs. This review examines various synthetic approaches and surface engineering strategies for preparing naked and functional iron oxide NPs with different physicochemical properties. Growing interest in designed and surface-engineered iron oxide NPs with multifunctionalities was explored in in vitro/in vivo biomedical applications, focusing on their combined roles in bioseparation, as a biosensor, targeted-drug delivery, MR contrast agents, and magnetic fluid hyperthermia. This review outlines the limitations of extant surface engineering strategies and several developing strategies that may overcome these limitations. This study also details the promising future directions of this active research field.

  5. The concept of delayed nucleation in nanocrystal growthdemonstrated for the case of iron oxide nanodisks

    Energy Technology Data Exchange (ETDEWEB)

    Casula, Maria F.; Jun, Young-wook; Zaziski, David J.; Chan, EmoryM.; Corrias, Anna; Alivisatos, Paul A.

    2005-09-09

    A comprehensive study of iron oxide nanocrystal growth through non-hydrolitic, surfactant-mediated thermal reaction of iron pentacarbonyl and an oxidizer has been conducted, which includes size control, anisotropic shape evolution, and crystallographic phase transition of monodisperse iron oxide colloidal nanocrystals. The reaction was monitored by in situ UV-Vis spectroscopy taking advantage of the color change accompanying the iron oxide colloid formation allowing measurement of the induction time for nucleation. Features of the synthesis such as the size control and reproducibility are related to the occurrence of the observed delayed nucleation process. As a separate source of iron and oxygen is adopted, phase control could also be achieved by sequential injections of oxidizer.

  6. Solution voltammetry of 4 nm magnetite iron oxide nanoparticles.

    Science.gov (United States)

    Roberts, Joseph J P; Westgard, John A; Cooper, Laura M; Murray, Royce W

    2014-07-30

    The voltammetry of solution-dispersed magnetite iron oxide Fe3O4 nanoparticles is described. Their currents are controlled by nanoparticle transport rates, as shown with potential step chronoamperometry and rotated disk voltammetry. In pH 2 citrate buffer with added NaClO4 electrolyte, solution cyclic voltammetry of these nanoparticles (average diameter 4.4 ± 0.9 nm, each containing ca. 30 Fe sites) displays an electrochemically irreversible oxidation with E(PEAK) at ca. +0.52 V and an irreversible reduction with E(PEAK) at ca. +0.2 V vs Ag/AgCl reference electrode. These processes are presumed to correspond to the formal potentials for one-electron oxidation of Fe(II) and reduction of Fe(III) at their different sites in the magnetite nanoparticle structure. The heterogeneous electrode reaction rates of the nanoparticles are very slow, in the 10(-5) cm/s range. The nanoparticles are additionally characterized by a variety of tools, e.g., TEM, UV/vis, and XPS spectroscopies.

  7. Processing, Microstructure, and Oxidation Behavior of Iron Foams

    Science.gov (United States)

    Park, Hyeji; Noh, Yoonsook; Choi, Hyelim; Hong, Kicheol; Kwon, Kyungjung; Choe, Heeman

    2016-09-01

    With its historically long popularity in major structural applications, the use of iron (Fe) has also recently begun to be explored as an advanced functional material. For this purpose, it is more advantageous to use Fe as a porous structure, simply because it can provide a greater surface area and a higher reaction rate. This study uses a freeze-casting method, which consists of simple and low-cost processing steps, to produce Fe foam with a mean pore size of 10 μm. We examine the influences of various parameters ( i.e., mold bottom temperature, powder content, and sintering time) on the processing of Fe foam, along with its oxidation kinetics at 823 K (550 °C) with various heat-treatment times. We confirm that Fe2O3 and Fe3O4 oxide layers are successfully formed on the surface of Fe foam. With the Fe oxide layers as an active anode material, the Fe foam can potentially be used as a three-dimensional anode current collector for an advanced lithium-ion battery.

  8. Iron and carbon metabolism by a mineral-oxidizing Alicyclobacillus-like bacterium.

    Science.gov (United States)

    Yahya, Adibah; Hallberg, Kevin B; Johnson, D Barrie

    2008-04-01

    A novel iron-oxidizing, moderately thermophilic, acidophilic bacterium (strain "GSM") was isolated from mineral spoil taken from a gold mine in Montana. Biomolecular analysis showed that it was most closely related to Alicyclobacillus tolerans, although the two bacteria differed in some key respects, including the absence (in strain GSM) of varpi-alicyclic fatty acids and in their chromosomal base compositions. Isolate GSM was able to grow in oxygen-free media using ferric iron as terminal electron acceptor confirming that it was a facultative anaerobe, a trait not previously described in Alicyclobacillus spp.. The acidophile used both organic and inorganic sources of energy and carbon, although growth and iron oxidation by isolate GSM was uncoupled in media that contained both fructose and ferrous iron. Fructose utilization suppressed iron oxidation, and oxidation of ferrous iron occurred only when fructose was depleted. In contrast, fructose catabolism was suppressed when bacteria were harvested while actively oxidizing iron, suggesting that both ferrous iron- and fructose-oxidation are inducible in this acidophile. Isolate GSM accelerated the oxidative dissolution of pyrite in liquid media either free of, or amended with, organic carbon, although redox potentials were significantly different in these media. The potential of this isolate for commercial mineral processing is discussed.

  9. Dielectrical and structural characterization of iron oxide added to hydroxyapatite

    Indian Academy of Sciences (India)

    C C Silva; F P Filho; M F P Graça; M A Valente; A S B Sombra

    2008-08-01

    In this work we report preparation, structural and dielectric analyses of iron oxide added in hydroxyapatite bioceramic (Ca10(PO4)6(OH)2 – HAP). Hydroxyapatite is the main mineral constituent of teeth and bones with excellent biocompatibility with hard and muscle tissues. The samples were prepared through a calcination procedure associated with dry high-energy ball milling process with different iron concentrations (1, 2.5 and 5 wt%). The dielectric analyses were made measuring the sample impedance in the frequency range 1 kHz–10 MHz, at room temperature. The relative permittivity of the ceramics, at 10 MHz, are between 7.13 ± 0.07 (1 wt%) and 6.20 ± 0.11 (5 wt%) while e″ are between 0.0795 ± 0.008 (1 wt%) and 0.067 ± 0.012 (5 wt%). These characteristics were related to the sample microstructures studied by X-ray diffraction and SEM.

  10. Synthesis, characterization and mechanistic insights of mycogenic iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Bhargava, Arpit; Jain, Navin; Manju Barathi L [Birla Institute of Technology and Science, Centre for Biotechnology, Department of Biological Sciences (India); Akhtar, Mohd Sayeed [Jimma University, Department of Applied Microbiology, College of Natural Sciences (Ethiopia); Yun, Yeoung-Sang [Chonbuk National University, Division of Environmental and Chemical Engineering (Korea, Republic of); Panwar, Jitendra, E-mail: drjitendrapanwar@yahoo.co.in [Birla Institute of Technology and Science, Centre for Biotechnology, Department of Biological Sciences (India)

    2013-11-15

    In the present study, extracellular synthesis of iron oxide nanoparticles (IONPs) was achieved using Aspergillus japonicus isolate AJP01. The isolate demonstrated its ability to hydrolyze the precursor salt solution, a mixture of iron cyanide complexes, under ambient conditions. Hydrolysis of these complexes released ferric and ferrous ions, which underwent protein-mediated coprecipitation and controlled nucleation resulting in the formation of IONPs. Transmission electron microscopy, selected area electron diffraction pattern, energy dispersive spectroscopy and grazing incidence X-ray diffraction analysis confirmed the mycosynthesis of IONPs. The synthesized particles were cubic in shape with a size range of 60–70 nm with crystal structure corresponding to magnetite. Scanning electron microscopy analysis revealed the absence of IONPs on fungal biomass surface, indicating the extracellular nature of synthesis. Fourier transform infrared spectroscopy confirmed the presence of proteins on as-synthesised IONPs, which may confer their stability. Preliminary investigation indicated the role of proteins in the synthesis and stabilization of IONPs. On the basis of present findings, a probable mechanism for synthesis of IONPs is suggested. The simplicity and versatility of the present approach can be utilized for the synthesis of other nanomaterials.

  11. Ca alginate as scaffold for iron oxide nanoparticles synthesis

    Directory of Open Access Journals (Sweden)

    P. V. Finotelli

    2008-12-01

    Full Text Available Recently, nanotechnology has developed to a stage that makes it possible to process magnetic nanoparticles for the site-specific delivery of drugs. To this end, it has been proposed as biomaterial for drug delivery system in which the drug release rates would be activated by a magnetic external stimuli. Alginate has been used extensively in the food, pharmaceutical and biomedical industries for their gel forming properties in the presence of multivalent cations. In this study, we produced iron oxide nanoparticles by coprecipitation of Fe(III and Fe(II. The nanoparticles were entrapped in Ca alginate beads before and after alginate gelation. XRD analysis showed that particles should be associated to magnetite or maghemite with crystal size of 9.5 and 4.3 nm, respectively. Studies using Mössbauer spectroscopy corroborate the superparamagnetic behavior. The combination of magnetic properties and the biocompatibility of alginate suggest that this biomaterial may be used as biomimetic system.

  12. Synthesis of Monodisperse Iron Oxide Nanoparticles without Surfactants

    Directory of Open Access Journals (Sweden)

    Xiao-Chen Yang

    2014-01-01

    Full Text Available Monodisperse iron oxide nanoparticles could be successfully synthesized with two kinds of precipitants through a precipitation method. As-prepared nanoparticles in the size around 10 nm with regular spherical-like shape were achieved by adjusting pH values. NaOH and NH3·H2O were used as two precipitants for comparison. The average size of nanoparticles with NH3·H2O precipitant got smaller and represented better dispersibility, while nanoparticles with NaOH precipitant represented better magnetic property. This work provided a simple method without using any organic solvents, organic metal salts, or surfactants which could easily obtain monodisperse nanoparticles with tunable morphology.

  13. Iron oxide nanoparticles stabilized inside highly ordered mesoporous silica

    Indian Academy of Sciences (India)

    A Bhaumik; S Samanta; N K Mal

    2005-11-01

    Nanosized iron oxide, a moderately large band-gap semiconductor and an essential component of optoelectrical and magnetic devices, has been prepared successfully inside the restricted internal pores of mesoporous silica material through in-situ reduction during impregnation. The samples were characterized by powder XRD, TEM, SEM/EDS, N2 adsorption, FT-IR and UV–visible spectroscopies. Characterization data indicated well-dispersed isolated nanoclusters of (Fe2O3),` within the internal surface of 2D-hexagonal mesoporous silica structure. No occluded Fe/Fe2O3 crystallites were observed at the external surface of the mesoporous silica nanocomposites. Inorganic mesoporous host, such as hydrophilic silica in the pore walls, directs a physical constraint necessary to prevent the creation of large Fe2O3 agglomerates and enables the formation of nanosized Fe2O3 particles inside the mesopore.

  14. Genotoxicity of Superparamagnetic Iron Oxide Nanoparticles in Granulosa Cells

    Directory of Open Access Journals (Sweden)

    Marina Pöttler

    2015-11-01

    Full Text Available Nanoparticles that are aimed at targeting cancer cells, but sparing healthy tissue provide an attractive platform of implementation for hyperthermia or as carriers of chemotherapeutics. According to the literature, diverse effects of nanoparticles relating to mammalian reproductive tissue are described. To address the impact of nanoparticles on cyto- and genotoxicity concerning the reproductive system, we examined the effect of superparamagnetic iron oxide nanoparticles (SPIONs on granulosa cells, which are very important for ovarian function and female fertility. Human granulosa cells (HLG-5 were treated with SPIONs, either coated with lauric acid (SEONLA only, or additionally with a protein corona of bovine serum albumin (BSA; SEONLA-BSA, or with dextran (SEONDEX. Both micronuclei testing and the detection of γH2A.X revealed no genotoxic effects of SEONLA-BSA, SEONDEX or SEONLA. Thus, it was demonstrated that different coatings of SPIONs improve biocompatibility, especially in terms of genotoxicity towards cells of the reproductive system.

  15. Superparamagnetic iron oxide nanoparticles (SPIONs) for targeted drug delivery

    Science.gov (United States)

    Garg, Vijayendra K.; Kuzmann, Erno; Sharma, Virender K.; Kumar, Arun; Oliveira, Aderbal C.

    2016-10-01

    Studies of superparamagnetic iron oxide nanoparticles (SPIONs) have been extensively carried out. Since the earlier work on Mössbauer studies on SPIONs in 1970s, many biomedical applications and their uses in innovative methods to produce new materials with improved performance have appeared. Applications of SPIONs in environmental remediation are also forthcoming. Several different methods of synthesis and coating of the magnetic particles have been described in the literature, and Mössbauer spectroscopy has been an important tool in the characterization of these materials. It is quite possible that the interpretation of the Mössbauer spectra might not be entirely correct because the possible presence of maghemite in the end product of SPIONs might not have been taken into consideration. Nanotechnology is an emerging field that covers a wide range of new technologies under development in nanoscale (1 to 100 nano meters) to produce new products and methodology.

  16. SURFACE-MODIFICATION OF FINE RED IRON OXIDE PIGMENT

    Institute of Scientific and Technical Information of China (English)

    Shuilin Zheng; Qinghui Zhang

    2003-01-01

    Surface-modification of fine red iron oxide pigment was carried out in an aqueous solution of sodium polyacrylate. The sedimentation time of modified samples in water increased from 1.05 to 264.4 hours while the particle size (d50) decreased from 1.09 to 0.85 μm, and the tinting strength increased from 100 to 115. The surface-modification as well as the dispersing and stabilizing mechanisms in aqueous solution of the samples were studied by means of IR,Thermal analysis and Zeta potential. The results showed that the modifier molecules acted on the surface of the particles by chemical and physical adsorption, and after the particles were dispersed in aqueous solution, endowing the particle surface with a relatively high negative Zeta potential, thus enhancing electrostatic and steric repulsion between particles for their effective stabilization.

  17. Mutagenic Effects of Iron Oxide Nanoparticles on Biological Cells.

    Science.gov (United States)

    Dissanayake, Niluka M; Current, Kelley M; Obare, Sherine O

    2015-09-30

    In recent years, there has been an increased interest in the design and use of iron oxide materials with nanoscale dimensions for magnetic, catalytic, biomedical, and electronic applications. The increased manufacture and use of iron oxide nanoparticles (IONPs) in consumer products as well as industrial processes is expected to lead to the unintentional release of IONPs into the environment. The impact of IONPs on the environment and on biological species is not well understood but remains a concern due to the increased chemical reactivity of nanoparticles relative to their bulk counterparts. This review article describes the impact of IONPs on cellular genetic components. The mutagenic impact of IONPs may damage an organism's ability to develop or reproduce. To date, there has been experimental evidence of IONPs having mutagenic interactions on human cell lines including lymphoblastoids, fibroblasts, microvascular endothelial cells, bone marrow cells, lung epithelial cells, alveolar type II like epithelial cells, bronchial fibroblasts, skin epithelial cells, hepatocytes, cerebral endothelial cells, fibrosarcoma cells, breast carcinoma cells, lung carcinoma cells, and cervix carcinoma cells. Other cell lines including the Chinese hamster ovary cells, mouse fibroblast cells, murine fibroblast cells, Mytilus galloprovincialis sperm cells, mice lung cells, murine alveolar macrophages, mice hepatic and renal tissue cells, and vero cells have also shown mutagenic effects upon exposure to IONPs. We further show the influence of IONPs on microorganisms in the presence and absence of dissolved organic carbon. The results shed light on the OPEN ACCESS Int. J. Mol. Sci. 2015, 16 23483 transformations IONPs undergo in the environment and the nature of the potential mutagenic impact on biological cells.

  18. Water oxidation catalysis by birnessite@iron oxide core-shell nanocomposites.

    Science.gov (United States)

    Elmaci, Gökhan; Frey, Carolin E; Kurz, Philipp; Zümreoğlu-Karan, Birgül

    2015-03-16

    In this work, magnetic nanocomposite particles were prepared for water oxidation reactions. The studied catalysts consist of maghemite (γ-Fe2O3), magnetite (Fe3O4), and manganese ferrite (MnFe2O4) nanoparticles as cores coated in situ with birnessite-type manganese oxide shells and were characterized by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, thermal, chemical, and surface analyses, and magnetic measurements. The particles were found to be of nearly spherical core-shell architectures with average diameter of 150 nm. Water oxidation catalysis was examined using Ce(4+) as the sacrificial oxidant. All core-shell particles were found to be active water oxidation catalysts. However, the activity was found to depend on a variety of factors like the type of iron oxide core, the structure and composition of the shell, the coating characteristics, and the surface properties. Catalysts containing magnetite and manganese ferrite as core materials displayed higher catalytic activities per manganese ion (2650 or 3150 mmolO2 molMn(-1) h(-1)) or per mass than nanoiron oxides (no activity) or birnessite alone (1850 mmolO2 molMn(-1) h(-1)). This indicates synergistic effects between the MnOx shell and the FeOx core of the composites and proves the potential of the presented core-shell approach for further catalyst optimization. Additionally, the FeOx cores of the particles allow magnetic recovery of the catalyst and might also be beneficial for applications in water-oxidizing anodes because the incorporation of iron might enhance the overall conductivity of the material.

  19. Biotic and abiotic oxidation and reduction of iron at circumneutral pH are inseparable processes under natural conditions

    NARCIS (Netherlands)

    Ionescu, Danny; Heim, Christine; Polerecky, L.; Thiel, Volker; de Beer, Dirk

    2015-01-01

    Oxidation and reduction of iron can occur through abiotic (chemical) and biotic (microbial) processes. Abiotic iron oxidation is a function of pH and O2 concentration. Biotic iron oxidation is carried out by a diverse group of bacteria, using O2 or NO3 as terminal electron acceptors. At circumneutra

  20. Ultrasonic-assisted synthesis and magnetic studies of iron oxide/MCM-41 nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Ursachi, Irina [Department of Physics ' Alexandru Ioan Cuza' University of Iasi, 11 Carol I Boulevard, 700506 Iasi (Romania); Vasile, Aurelia [Department of Chemistry, ' Alexandru Ioan Cuza' University of Iasi, 11 Carol I Boulevard, 700506 Iasi (Romania); Ianculescu, Adelina [Department of Oxide Materials and Engineering, Polytechnics University of Bucharest, 1-7 Gh. Polizu, 011061 Bucharest (Romania); Vasile, Eugeniu [METAV S.A., Research and Development, 31 C.A. Rosetti, 020011, Bucharest (Romania); Stancu, Alexandru, E-mail: alstancu@uaic.ro [Department of Physics ' Alexandru Ioan Cuza' University of Iasi, 11 Carol I Boulevard, 700506 Iasi (Romania)

    2011-11-01

    Highlights: {yields} A quick and facile route for the synthesis of iron oxide/MCM-41 nanocomposite. {yields} Magnetic nanoparticles were stabilized inside the pores of mesoporous silica MCM-41. {yields} The pore size of MCM-41 dictates the properties of iron oxide nanoparticles. {yields} The procedure provides a narrow size distribution of magnetic nanoparticles. - Abstract: Iron oxide nanoparticles were stabilized within the pores of mesoporous silica MCM-41 amino-functionalized by a sonochemical method. Formation of iron oxide nanoparticles inside the mesoporous channels of amino-functionalized MCM-41 was realized by wet impregnation using iron nitrate, followed by calcinations at 550 deg. C in air. The effect of functionalization level on structural and magnetic properties of obtained nanocomposites was studied. The resulting materials were characterized by powder X-ray diffraction (XRD), high-resolution transmission electron microscopy and selected area electron diffraction (HRTEM and SAED), vibrating sample and superconducting quantum interface magnetometers (VSM and SQUID) and nitrogen adsorption-desorption isotherms measurements. The HRTEM images reveal that the most of the iron oxide nanoparticles were dispersed inside the mesopores of silica matrix and the pore diameter of the amino-functionalized MCM-41 matrix dictates the particle size of iron oxide nanoparticles. The obtained material possesses mesoporous structure and interesting magnetic properties. Saturation magnetization value of magnetic iron oxide nanopatricles stabilized in MCM-41 amino-functionalized by in situ sonochemical synthesis was 1.84 emu g{sup -1}. An important finding is that obtained magnetic nanocomposite materials exhibit enhanced magnetic properties than those of iron oxide/MCM-41 nanocomposite obtained by conventional method. The described method is providing a rather short preparation time and a narrow size distribution of iron oxide nanoparticles.

  1. Deposition and Characterization of Sisal Fiber Composite Prepare By Iron Oxide Synthesis.

    Directory of Open Access Journals (Sweden)

    Asif Jehan

    2015-02-01

    Full Text Available Iron oxide synthesized through sintering route. The present research work deals with ferrite composite prepared using chemical reactions. Ferric nitrates and ammonium chloride doped with sisal fiber has been prepared. The comparative studies of ferric oxide were examined through few characterizations. The structural behavior of iron oxide was studied in XRD, FT/IR, TEM and SEM. This behavior showed ferrite nature of the sample.

  2. Effect of Iron Enriched Bread Intake on the Oxidative Stress Indices in Male Wistar Rats

    Directory of Open Access Journals (Sweden)

    Sharareh Heidari

    2016-08-01

    Full Text Available Background Contrary to the proven benefits of iron, few concerns in producing the oxidative stress is remained problematic. Objectives The aim of the study was to evaluate the oxidative stress in the male Wistar rats fed bread supplemented with iron in different doses i.e., 35 (basic, 70 (two fold, 140 (four fold, and 210 mg/kg (six fold with or without NaHCO3 (250 mg/kg. Methods In this experimental study Iron, ceruloplasmin, ferritin, total iron binding capacity (TIBC, albumin, total protein, uric acid and plasma superoxide dismutase (SOD, glutathione peroxidase (GPX, catalase (CAT, malondialdehyde (MDA, and total antioxidant capacity (TAC, were evaluated in 30 rats at the first and last day of the experiment (day 30. In addition, phytic acid levels were detected in all baked breads. The data were analyzed by ANOVA and t test procedure though SPSS statistical software version 20. Results Serum iron level in rats that received basic level of iron plus NaHCO3 decreased significantly in the last day of the trial. Higher level of serum iron was seen in rats that received iron twofold, fourfold and sixfold and rats that received iron fourfold plus NaHCO3. Serum ceruloplasmin and ferritin in groups of rats that received fourfold level of iron plus NaHCO3 and rats that received iron sixfold showed a significant increase (P ≤ 0.05. Serum total protein and uric acid in rats that received basic level of iron plus NaHCO3 and rats that received twofold level of iron showed a significant decrease. Serum total protein levels in rats that received fourfold level of iron showed a significant decrease. Bread with NaHCO3 showed higher phytic acid levels than other groups. Conclusions These results indicate that oxidative stress was not induced, whereas some antioxidant activities were significantly changed in rats that received iron-enriched bread.

  3. Uncoupling and oxidative stress in liver mitochondria isolated from rats with acute iron overload

    Energy Technology Data Exchange (ETDEWEB)

    Pardo Andreu, G.L. [Centro de Quimica Farmaceutica, Departamento de Investigaciones Biomedicas, Ciudad de La Habana (Cuba); Inada, N.M.; Vercesi, A.E. [Universidade Estadual de Campinas, Departamento de Patologia Clinica, Faculdade de Ciencias Medicas, Campinas, SP (Brazil); Curti, C. [Universidade de Sao Paulo, Departamento de Fisica e Quimica, Faculdade de Ciencias Farmaceuticas de Ribeirao Preto, SP (Brazil)

    2009-01-15

    One hypothesis for the etiology of cell damage arising from iron overload is that its excess selectively affects mitochondria. Here we tested the effects of acute iron overload on liver mitochondria isolated from rats subjected to a single dose of i.p. 500 mg/kg iron-dextran. The treatment increased the levels of iron in mitochondria (from 21{+-}4 to 130{+-}7 nmol/mg protein) and caused both lipid peroxidation and glutathione oxidation. The mitochondria of iron-treated rats showed lower respiratory control ratio in association with higher resting respiration. The mitochondrial uncoupling elicited by iron-treatment did not affect the phosphorylation efficiency or the ATP levels, suggesting that uncoupling is a mitochondrial protective mechanism against acute iron overload. Therefore, the reactive oxygen species (ROS)/H{sup +} leak couple, functioning as a mitochondrial redox homeostatic mechanism could play a protective role in the acutely iron-loaded mitochondria. (orig.)

  4. Biocompatible capped iron oxide nanoparticles for Vibrio cholerae detection

    Science.gov (United States)

    Sharma, Anshu; Baral, Dinesh; Rawat, Kamla; Solanki, Pratima R.; Bohidar, H. B.

    2015-05-01

    We report the studies relating to fabrication of an efficient immunosensor for Vibrio cholerae detection. Magnetite (iron oxide (Fe3O4)) nanoparticles (NPs) have been synthesized by the co-precipitation method and capped by citric acid (CA). These NPs were electrophoretically deposited onto indium-tin-oxide (ITO)-coated glass substrate and used for immobilization of monoclonal antibodies against Vibrio cholerae (Ab) and bovine serum albumin (BSA) for Vibrio cholerae detection using an electrochemical technique. The structural and morphological studies of Fe3O4 and CA-Fe3O4/ITO were characterized by x-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, and dynamic light scattering (DLS) techniques. The average crystalline size of Fe3O4, CA-Fe3O4 nanoparticles obtained were about 29 ± 1 nm and 37 ± 1 nm, respectively. The hydrodynamic radius of the nanoparticles was found to be 77.35 nm (Fe3O4) and 189.51 nm (CA-Fe3O4) by DLS measurement. The results of electrochemical response studies of the fabricated BSA/Ab/CA-Fe2O3/ITO immunosensor exhibits a good detection range of 12.5-500 ng mL-1 with a low detection limit of 0.32 ng mL-1, sensitivity 0.03 Ω/ng ml-1 cm-2, and reproducibility more than 11 times.

  5. Concentration-dependent toxicity of iron oxide nanoparticles mediated by increased oxidative stress

    Directory of Open Access Journals (Sweden)

    Saba Naqvi

    2010-11-01

    Full Text Available Saba Naqvi1, Mohammad Samim2, MZ Abdin3, Farhan Jalees Ahmed4, AN Maitra5, CK Prashant6, Amit K Dinda61Faculty of Engineering and Interdisciplinary Sciences, 2Department of Chemistry, 3Department of Biotechnology, Faculty of Science, 4Department of Pharmaceutics, Faculty of Pharmacy, Jamia Hamdard, Hamdard University, 5Department of Chemistry, University of Delhi, 6Department of Pathology, All India Institute of Medical Sciences, New Delhi, IndiaAbstract: Iron oxide nanoparticles with unique magnetic properties have a high potential for use in several biomedical, bioengineering and in vivo applications, including tissue repair, magnetic resonance imaging, immunoassay, drug delivery, detoxification of biologic fluids, cell sorting, and hyperthermia. Although various surface modifications are being done for making these nonbiodegradable nanoparticles more biocompatible, their toxic potential is still a major concern. The current in vitro study of the interaction of superparamagnetic iron oxide nanoparticles of mean diameter 30 nm coated with Tween 80 and murine macrophage (J774 cells was undertaken to evaluate the dose- and time-dependent toxic potential, as well as investigate the role of oxidative stress in the toxicity. A 15–30 nm size range of spherical nanoparticles were characterized by transmission electron microscopy and zeta sizer. MTT assay showed >95% viability of cells in lower concentrations (25–200 µg/mL and up to three hours of exposure, whereas at higher concentrations (300–500 µg/mL and prolonged (six hours exposure viability reduced to 55%–65%. Necrosis-apoptosis assay by propidium iodide and Hoechst-33342 staining revealed loss of the majority of the cells by apoptosis. H2DCFDDA assay to quantify generation of intracellular reactive oxygen species (ROS indicated that exposure to a higher concentration of nanoparticles resulted in enhanced ROS generation, leading to cell injury and death. The cell membrane injury

  6. Iron oxide nanoparticles synthesis through a benign approach and its catalytic application

    Directory of Open Access Journals (Sweden)

    Henam Sylvia Devi

    2016-09-01

    Full Text Available Synthesis of iron oxide nanoparticles was carried out through an environmental benign route using tannic acid as reducing and capping agent. The TEM image shows the details of the poly-dispersity in size of the iron oxide nanoparticle and average diameter of the particles range in between 30 and 50 nm. XRD result rule out that iron oxide nanoparticle is a mixed phase constituted by Fe+2 and Fe+3 ions. The average size of the particle determined from XRD data is 45.6 nm which is agreeable with the finding obtained from TEM images. This particle of iron oxide is used for the degradation of p-cresol and it successfully degraded p-cresol. Catalytic property of the iron oxide nanoparticle was also investigation using methylene blue as role model dye. Degradation of methylene blue dye was studied in presence of NaBH4 and the degradation reaction followed first order kinetics with rate constant value of 1.6 × 10−3 min−1. The rate constant of the reaction in absence of iron oxide nanoparticles is 4 × 10−4 min−1, this result confirmed the catalytic nature of as such prepared iron oxide nanoparticles.

  7. Evaluation of the properties of iron oxide-filled castor oil polyurethane

    Directory of Open Access Journals (Sweden)

    Eleonora Mussatti

    2013-02-01

    Full Text Available The aim of this study was to obtain and evaluate the electrical, thermal and mechanical properties of iron oxide-filled castor oil polyurethane (PU/Fe2O3. The iron oxide used in this study was a residue derived from the steel pickling process of a Brazilian steel rolling industry. Polymeric composites with different iron oxide volume fractions (2.5, 5.0, 7.5, 10.0 and 12.5% were prepared through the casting process followed by compression molding at room temperature. The composites were analyzed by FTIR, XRD and densities, tensile strength, Young's modulus, electrical and thermal conductivities measurements. By increasing the iron oxide content, the apparent density, tensile strength, Young's modulus and electrical conductivity values of the composites were also increased. The iron oxide additions did not change significantly the value of thermal conductivity (from 0.191 W.mK-1 for PU up to 0.340 W.mK-1 for PU enriched with 12.5% v/v of iron oxide. Thus, even at the higher iron oxide concentration, the compounds as well as the pure polyurethane can be classified as thermal insulators.

  8. Catalytic performance of cerium iron complex oxides for partial oxidation of methane to synthesis gas

    Institute of Scientific and Technical Information of China (English)

    LI Kongzhai; WANG Hua; WEI Yonggang; LIU Mingchun

    2008-01-01

    The cerium iron complex oxides oxygen carder was prepared by the co-precipitation method. The reactions between methane and lattice oxygen from the complex oxides were investigated in a fixed micro-reactor system. The reduced oxygen carrier could be re-oxidized by air and its initial state could be restored. The characterizations of the oxygen carriers were studied using XRD, O2-TPD, and H2-TPR. The results showed that the bulk lattice oxygen of CeO2-Fe2O3 was found to be suitable for the partial oxidation of methane to synthesis gas. There were two kinds of oxygen species on the oxygen carder: the stronger oxygen species that was responsible for the complete oxidation of methane, and the weaker oxygen species (bulk lattice oxygen) that was responsible for the selective oxidation of methane to CO and H2 at a higher temperature. Then, the lost bulk lattice oxygen could be selectively supplemented by air re-oxidation at an appropriate reaction con-dition. CeFeO3 appeared on the oxygen carrier after 10 successive redox cycles, however, it was not bad for the selectivity of CO and H2.

  9. Iron supplementation at high altitudes induces inflammation and oxidative injury to lung tissues in rats

    Energy Technology Data Exchange (ETDEWEB)

    Salama, Samir A., E-mail: salama.3@buckeyemail.osu.edu [High Altitude Research Center, Taif University, Al-Haweiah, Taif 21974 (Saudi Arabia); Department of Biochemistry, Faculty of Pharmacy, Al-Azhar University, Cairo 11751 (Egypt); Department of Pharmacology and GTMR Unit, College of Clinical Pharmacy, Taif University, Al-Haweiah, Taif 21974 (Saudi Arabia); Omar, Hany A. [Department of Pharmacology, Faculty of Pharmacy, Beni-Suef University, Beni-Suef 62514 (Egypt); Maghrabi, Ibrahim A. [Department of Clinical Pharmacy, College of Clinical Pharmacy, Taif University, Al-Haweiah, Taif 21974 (Saudi Arabia); AlSaeed, Mohammed S. [Department of Surgery, College of Medicine, Taif University, Al-Haweiah, Taif 21974 (Saudi Arabia); EL-Tarras, Adel E. [High Altitude Research Center, Taif University, Al-Haweiah, Taif 21974 (Saudi Arabia)

    2014-01-01

    Exposure to high altitudes is associated with hypoxia and increased vulnerability to oxidative stress. Polycythemia (increased number of circulating erythrocytes) develops to compensate the high altitude associated hypoxia. Iron supplementation is, thus, recommended to meet the demand for the physiological polycythemia. Iron is a major player in redox reactions and may exacerbate the high altitudes-associated oxidative stress. The aim of this study was to explore the potential iron-induced oxidative lung tissue injury in rats at high altitudes (6000 ft above the sea level). Iron supplementation (2 mg elemental iron/kg, once daily for 15 days) induced histopathological changes to lung tissues that include severe congestion, dilatation of the blood vessels, emphysema in the air alveoli, and peribronchial inflammatory cell infiltration. The levels of pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α), lipid peroxidation product and protein carbonyl content in lung tissues were significantly elevated. Moreover, the levels of reduced glutathione and total antioxidant capacity were significantly reduced. Co-administration of trolox, a water soluble vitamin E analog (25 mg/kg, once daily for the last 7 days of iron supplementation), alleviated the lung histological impairments, significantly decreased the pro-inflammatory cytokines, and restored the oxidative stress markers. Together, our findings indicate that iron supplementation at high altitudes induces lung tissue injury in rats. This injury could be mediated through excessive production of reactive oxygen species and induction of inflammatory responses. The study highlights the tissue injury induced by iron supplementation at high altitudes and suggests the co-administration of antioxidants such as trolox as protective measures. - Highlights: • Iron supplementation at high altitudes induced lung histological changes in rats. • Iron induced oxidative stress in lung tissues of rats at high altitudes. • Iron

  10. Whey protein inhibits iron overload-induced oxidative stress in rats.

    Science.gov (United States)

    Kim, Jungmi; Paik, Hyun-Dong; Yoon, Yoh-Chang; Park, Eunju

    2013-01-01

    In this study, we evaluated the effects of whey protein on oxidative stress in rats that were subjected to oxidative stress induced by iron overload. Thirty male rats were assigned to 3 groups: the control group (regular [50 mg/kg diet] dose of iron+20% casein), iron overload group (high [2,000 mg/kg] dose of iron+20% casein, IO), and whey protein group (high dose of iron+10% casein+10% whey protein, IO+whey). After 6 wk, the IO group showed a reduction in the plasma total radical trapping antioxidant parameter and the activity of erythrocyte superoxide dismutase and an increase in lipid peroxidation (determined from the proportion of conjugated dienes). However, whey protein ameliorated the oxidative changes induced by iron overload. The concentration of erythrocyte glutathione was significantly higher in the IO+whey group than in the IO group. In addition, whey protein supplementation fully inhibited iron overload-induced DNA damage in leukocytes and colonocytes. A highly significant positive correlation was observed between plasma iron levels and DNA damage in leukocytes and colonocytes. These results show the antioxidative and antigenotoxic effects of whey protein in an in vivo model of iron overload-induced oxidative stress.

  11. Secoisolariciresinol diglucoside abrogates oxidative stress-induced damage in cardiac iron overload condition.

    Directory of Open Access Journals (Sweden)

    Stephanie Puukila

    Full Text Available Cardiac iron overload is directly associated with cardiac dysfunction and can ultimately lead to heart failure. This study examined the effect of secoisolariciresinol diglucoside (SDG, a component of flaxseed, on iron overload induced cardiac damage by evaluating oxidative stress, inflammation and apoptosis in H9c2 cardiomyocytes. Cells were incubated with 50 μ5M iron for 24 hours and/or a 24 hour pre-treatment of 500 μ M SDG. Cardiac iron overload resulted in increased oxidative stress and gene expression of the inflammatory mediators tumor necrosis factor-α, interleukin-10 and interferon γ, as well as matrix metalloproteinases-2 and -9. Increased apoptosis was evident by increased active caspase 3/7 activity and increased protein expression of Forkhead box O3a, caspase 3 and Bax. Cardiac iron overload also resulted in increased protein expression of p70S6 Kinase 1 and decreased expression of AMP-activated protein kinase. Pre-treatment with SDG abrogated the iron-induced increases in oxidative stress, inflammation and apoptosis, as well as the increased p70S6 Kinase 1 and decreased AMP-activated protein kinase expression. The decrease in superoxide dismutase activity by iron treatment was prevented by pre-treatment with SDG in the presence of iron. Based on these findings we conclude that SDG was cytoprotective in an in vitro model of iron overload induced redox-inflammatory damage, suggesting a novel potential role for SDG in cardiac iron overload.

  12. Influence of Fe(2+)-catalysed iron oxide recrystallization on metal cycling.

    Science.gov (United States)

    Latta, Drew E; Gorski, Christopher A; Scherer, Michelle M

    2012-12-01

    Recent work has indicated that iron (oxyhydr-)oxides are capable of structurally incorporating and releasing metals and nutrients as a result of Fe2+-induced iron oxide recrystallization. In the present paper, we briefly review the current literature examining the mechanisms by which iron oxides recrystallize and summarize how recrystallization affects metal incorporation and release. We also provide new experimental evidence for the Fe2+-induced release of structural manganese from manganese-doped goethite. Currently, the exact mechanism(s) for Fe2+-induced recrystallization remain elusive, although they are likely to be both oxide-and metal-dependent. We conclude by discussing some future research directions for Fe2+-catalysed iron oxide recrystallization.

  13. Gold catalysts supported on nanosized iron oxide for low-temperature oxidation of carbon monoxide and formaldehyde

    Science.gov (United States)

    Tang, Zheng; Zhang, Weidong; Li, Yi; Huang, Zuming; Guo, Huishan; Wu, Feng; Li, Jinjun

    2016-02-01

    This study aimed to optimize synthesis of gold catalyst supported on nanosized iron oxide and to evaluate the activity in oxidation of carbon monoxide and formaldehyde. Nanosized iron oxide was prepared from a colloidal dispersion of hydrous iron oxide through a dispersion-precipitation method. Gold was adsorbed onto nanosized iron oxide under self-generated basic conditions. Characterization results indicate that the iron oxide consisted of hematite/maghemite composite with primary particle sizes of 6-8 nm. Gold was highly dispersed on the surface of the support. The catalysts showed good activity in the oxidation of airborne carbon monoxide and formaldehyde. The optimal pH for their synthesis was ∼7. The catalytic performance could be enhanced by extending the adsorption time of gold species on the support within 21 h. The optimized catalyst was capable of achieving complete oxidation of 1% carbon monoxide at -20 °C and 33% conversion of 450 ppm formaldehyde at ambient temperature. The catalyst may be applicable to indoor air purification.

  14. Environment friendly route of iron oxide nanoparticles from Zingiber officinale (ginger) root extract

    Science.gov (United States)

    Xin Hui, Yau; Yi Peng, Teoh; Wei Wen, Liu; Zhong Xian, Ooi; Peck Loo, Kiew

    2016-11-01

    Iron oxide nanoparticles were prepared from the reaction between the Zingiber officinale (ginger) root extracts and ferric chloride solution at 50°C for 2 h in mild stirring condition. The synthesized powder forms of nanoparticles were further characterized by using UV-Vis spectroscopy and X-ray Diffraction spectrometry. UV-Vis analysis shows the absorption peak of iron oxide nanoparticles is appeared at 370 nm. The calculation of crystallite size from the XRD showed that the average particle size of iron oxide nanoparticles was 68.43 nm. Therefore, this eco-friendly technique is low cost and large scale nanoparticles synthesis to fulfill the demand of various applications.

  15. Early diagenetic quartz formation at a deep iron oxidation front in the Eastern Equatorial Pacific

    Science.gov (United States)

    Meister, Patrick; Chapligin, Bernhard; Picard, Aude; Meyer, Hanno; Fischer, Cornelius; Rettenwander, Daniel; Amthauer, Georg; Vogt, Christoph; Aiello, Ivano

    2015-04-01

    The mechanisms of early diagenetic quartz formation under low-temperature conditions are still poorly understood. We studied lithified cherts consisting of microcrystalline quartz recovered from ODP Site 1226 in the Eastern Equatorial Pacific. The cherts occur near the base of a 420-m-thick Miocene-Holocene sequence within unlithified nannofossil and diatom ooze. Palaeo-temperatures reconstructed from δ18O values in the cherts are near to present porewater temperatures and a sharp depletion in dissolved silica occurs around 385 mbsf indicating that silica precipitation is still ongoing. Also a deep iron oxidation front occurs at the same depth, which is caused by upward diffusing nitrate from an oxic seawater aquifer in the underlying basaltic crust. Sequential iron extraction and analysis of the X-ray absorption near-edge structure (XANES) revealed that iron in the cherts predominantly occurs as illite and amorphous iron oxide, whereas iron in the nannofossil and diatom ooze occurs mainly as smectites. Mössbauer spectroscopy confirmed that the illite iron in the cherts is largely oxidized. A possible mechanisms that may be operative is quartz precipitation initiated by adsorption of silica to freshly precipitated iron oxides. The decrease in porewater silica concentration below opal-A and opal-CT saturation then allows for the precipitation of the thermodynamically more stable phase: quartz. We suggest that the formation of early-diagenetic chert at iron oxidation fronts is an important process in suboxic zones of silica-rich sediments. The largest iron oxidation front ever occurred during the great oxidation event ca. 2.5 Ga ago, when large amounts of iron and chert beds were deposited.

  16. Physiological effects of magnetic iron oxide nanoparticles towards watermelon.

    Science.gov (United States)

    Li, Junli; Chang, Peter R; Huang, Jin; Wang, Yunqiang; Yuan, Hong; Ren, Hongxuan

    2013-08-01

    Nanoparticles (NPs) have been exploited in a diverse range of products in the past decade or so. However, the biosafety/environmental impact or legislation pertaining to this newly created, highly functional composites containing NPs (otherwise called nanomaterials) is generally lagging behind their technological innovation. To advance the agenda in this area, our current primary interest is focused on using crops as model systems as they have very close relationship with us. Thus, the objective of the present study was to evaluate the biological effects of magnetic iron oxide nanoparticles towards watermelon seedlings. We have systematically studied the physiological effects of Fe2O3 nanoparticles (nano-Fe2O3) on watermelon, and present the first evidence that a significant amount of Fe2O3 nanoparticles suspended in a liquid medium can be taken up by watermelon plants and translocated throughout the plant tissues. Changes in important physiological indicators, such as root activity, activity of catalase (CAT), peroxidase (POD) and superoxide dismutase (SOD), chlorophyll and malondialdehyde (MDA) contents, ferric reductase activity, root apoplastic iron content were clearly presented. Different concentrations of nano-Fe2O3 all increased seed germination, seedling growth, and enhanced physiological function to some degree; and the positive effects increased quickly and then slowed with an increase in the treatment concentrations. Changes in CAT, SOD and POD activities due to nano-Fe2O3 were significantly larger than that of the control. The 20 mg/L treatment had the most obvious effect on the increase of root activity. Ferric reductase activity, root apoplastic iron content, and watermelon biomass were significantly affected by exposure to nano-Fe2O3. Results of statistical analysis showed that there were significant differences in all the above indexes between the treatment at optimal concentration and the control. This proved that the proper concentration of nano

  17. The Influence of Iron Ions on the Aqueous Photocatalytic Oxidation of Deicing Agents

    Directory of Open Access Journals (Sweden)

    D. Klauson

    2007-01-01

    Full Text Available An experimental research into aqueous photocatalytic oxidation (PCO of the deicing compounds, 2-ethoxyethanol (2-EE, diethylene glycol monomethyl ether (DEGMME, and ethylene glycol (EG was undertaken. The addition of iron ions to the acidic aqueous solutions to be treated displayed complex influence on the oxidation efficiency of the above mentioned substances, resulting in a sharp increase of the PCO efficiency at smaller concentrations of iron ions followed by a drastic decrease with the increasing iron ion concentrations. The phenomena observed can be explained by the electron scavenging effect of the iron ions and the competitive adsorption of iron ions and the oxidized substances on titanium dioxide surface. The carbonic acids determined as the PCO by-products allow outlining some reaction pathways for the substances under consideration.

  18. Synthesis and characterization of iron oxide nanoparticles using electrical discharge in solution

    Directory of Open Access Journals (Sweden)

    B Mohammadi

    2017-02-01

    Full Text Available Iron oxide nanoparticles were synthesized for the first time using electrical arc discharge between a pair of highly pure titanium electrode without using metallic iron electrodes in iron chloride salt solution. The produced nanoparticles were characterized using various analyses such as X-ray Diffraction (XRD and X-ray Photoelectron Spectroscopy (XPS. XRD and XPS analyses showed formation of α-Fe2O3 phase. Microscopic studies on the obtained samples revealed formation of rice like iron oxide nanostructures at 10 minutes of electrical discharge which changed to semi-spherical shape after calcination at 600 oC for 2 hours. The results of Dynamic Light Scattering (DLS analysis demonstrated formation of 24 nm particles with almost narrow distribution of 11nm, which are increased in size and distribution width by heat treatment. The obtained results verify the potential ability of this technique to achieve monodispersed iron oxide nanoparticles with narrow distribution in a very short time

  19. Solvothermal synthesis and characterization of monodisperse superparamagnetic iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Li, Shichuan; Zhang, Tonglai; Tang, Runze; Qiu, Hao [State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081 (China); Wang, Caiqin [Shandong Special Industry Group Co., Ltd, Shandong 255201 (China); Zhou, Zunning [State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081 (China)

    2015-04-01

    A series of magnetic iron oxide nanoparticle clusters with different structure guide agents were synthesized by a modified solvothermal method and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), thermogravimetric analyses (TG), a vibrating sample magnetometer (VSM) and Fourier transform infrared spectroscopy (FTIR). It is found that the superparamagnetic nanoparticles guided by NaCit (sodium citrate) have high saturation magnetization (M{sub s}) of 69.641 emu/g and low retentivity (M{sub r}) of 0.8 emu/g. Guiding to form superparamagnetic clusters with size range of 80–110 nm, the adherent small-molecule citrate groups on the surface prevent the prefabricated ferrite crystals growing further. In contrast, the primary small crystal guided and stabilized by the PVP long-chain molecules assemble freely to larger ones and stop growing in size range of 100–150 nm, which has saturation magnetization (M{sub s}) of 97.979 emu/g and retentivity (M{sub r}) of 46.323 emu/g. The relevant formation mechanisms of the two types of samples are proposed at the end. The superparamagnetic ferrite clusters guided by sodium citrate are expected to be used for movement controlling of passive interference particles to avoid aggregation and the sample guided by PVP will be a candidate of nanometer wave absorbing material. - Highlights: • A facile synthesis of two kinds of monodisperse iron oxide nano-particle clusters was performed via a modified one-step solvothermal method in this work. • The NaCit and PVP as different guiding agents are used to control the formation and aggregation of nano-crystals during reacting and the ripening processes. • The superparamagnetic NaCit–Fe{sub 3}O{sub 4} samples have high saturation magnetization (M{sub s}) of 69.641 emu/g and low retentivity (M{sub r}) of 0.8 emu/g. • The relevant formation mechanisms of the two types of samples are proposed.

  20. Hawaiian submarine manganese-iron oxide crusts - A dating tool?

    Science.gov (United States)

    Moore, J.G.; Clague, D.A.

    2004-01-01

    Black manganese-iron oxide crusts form on most exposed rock on the ocean floor. Such crusts are well developed on the steep lava slopes of the Hawaiian Ridge and have been sampled during dredging and submersible dives. The crusts also occur on fragments detached from bedrock by mass wasting, on submerged coral reefs, and on poorly lithified sedimentary rocks. The thickness of the crusts was measured on samples collected since 1965 on the Hawaiian Ridge from 140 dive or dredge localities. Fifty-nine (42%) of the sites were collected in 2001 by remotely operated vehicles (ROVs). The thinner crusts on many samples apparently result from post-depositional breakage, landsliding, and intermittent burial of outcrops by sediment. The maximum crust thickness was selected from each dredge or dive site to best represent crusts on the original rock surface at that site. The measurements show an irregular progressive thickening of the crusts toward the northwest-i.e., progressive thickening toward the older volcanic features with increasing distance from the Hawaiian hotspot. Comparison of the maximum crust thickness with radiometric ages of related subaerial features supports previous studies that indicate a crust-growth rate of about 2.5 mm/m.y. The thickness information not only allows a comparison of the relative exposure ages of two or more features offshore from different volcanoes, but also provides specific age estimates of volcanic and landslide deposits. The data indicate that some of the landslide blocks within the south Kona landslide are the oldest exposed rock on Mauna Loa, Kilauea, or Loihi volcanoes. Crusts on the floors of submarine canyons off Kohala and East Molokai volcanoes indicate that these canyons are no longer serving as channelways for downslope, sediment-laden currents. Mahukona volcano was approximately synchronous with Hilo Ridge, both being younger than Hana Ridge. The Nuuanu landslide is considerably older than the Wailau landslide. The Waianae

  1. High Temperature Corrosion of Fe-C-S Cast Irons in Oxidizing and Sulfidizing Atmospheres

    Institute of Scientific and Technical Information of China (English)

    Thuan-Dinh NGUYEN; Dong-Bok LEE

    2008-01-01

    The corrosion behavior of spheroidal graphite and flake graphite cast irons was studied in oxidizing and sulfidizing atmospheres between 600 and 800℃ for 50 h. The corrosion rate in the sulfidizing atmosphere was faster than that in air above 700℃, due to the formation of the Feo.975S sulfide. The corrosion rate of the spheroidal graphite cast iron was similar to that of the flake graphite cast iron.

  2. Ribosomal RNA in Alzheimer disease is oxidized by bound redox-active iron.

    Science.gov (United States)

    Honda, Kazuhiro; Smith, Mark A; Zhu, Xiongwei; Baus, Diane; Merrick, William C; Tartakoff, Alan M; Hattier, Thomas; Harris, Peggy L; Siedlak, Sandra L; Fujioka, Hisashi; Liu, Quan; Moreira, Paula I; Miller, Frank P; Nunomura, Akihiko; Shimohama, Shun; Perry, George

    2005-06-03

    Oxidative modification of cytoplasmic RNA in vulnerable neurons is an important, well documented feature of the pathophysiology of Alzheimer disease. Here we report that RNA-bound iron plays a pivotal role for RNA oxidation in vulnerable neurons in Alzheimer disease brain. The cytoplasm of hippocampal neurons showed significantly higher redox activity and iron(II) staining than age-matched controls. Notably, both were susceptible to RNase, suggesting a physical association of iron(II) with RNA. Ultrastructural analysis further suggested an endoplasmic reticulum association. Both rRNA and mRNA showed twice the iron binding as tRNA. rRNA, extremely abundant in neurons, was considered to provide the greatest number of iron binding sites among cytoplasmic RNA species. Interestingly, the difference of iron binding capacity disappeared after denaturation of RNA, suggesting that the higher order structure may contribute to the greater iron binding of rRNA. Reflecting the difference of iron binding capacity, oxidation of rRNA by the Fenton reaction formed 13 times more 8-hydroxyguanosine than tRNA. Consistent with in situ findings, ribosomes purified from Alzheimer hippocampus contained significantly higher levels of RNase-sensitive iron(II) and redox activity than control. Furthermore, only Alzheimer rRNA contains 8-hydroxyguanosine in reverse transcriptase-PCR. Addressing the biological significance of ribosome oxidation by redox-active iron, in vitro translation with oxidized ribosomes from rabbit reticulocyte showed a significant reduction of protein synthesis. In conclusion these results suggest that rRNA provides a binding site for redox-active iron and serves as a redox center within the cytoplasm of vulnerable neurons in Alzheimer disease in advance of the appearance of morphological change indicating neurodegeneration.

  3. Spectroscopic investigation and direct comparison of the reactivities of iron pyridyl oxidation catalysts

    Science.gov (United States)

    Song, Yang; Mayes, Howard G.; Queensen, Matthew J.; Bauer, Eike B.; Dupureur, Cynthia M.

    2017-03-01

    The growing interest in green chemistry has fueled attention to the development and characterization of effective iron complex oxidation catalysts. A number of iron complexes are known to catalyze the oxidation of organic substrates utilizing peroxides as the oxidant. Their development is complicated by a lack of direct comparison of the reactivities of the iron complexes. To begin to correlate reactivity with structural elements, we compare the reactivities of a series of iron pyridyl complexes toward a single dye substrate, malachite green (MG), for which colorless oxidation products are established. Complexes with tetradentate, nitrogen-based ligands with cis open coordination sites were found to be the most reactive. While some complexes reflect sensitivity to different peroxides, others are similarly reactive with either H2O2 or tBuOOH, which suggests some mechanistic distinctions. [Fe(S,S-PDP)(CH3CN)2](SbF6)2 and [Fe(OTf)2(tpa)] transition under the oxidative reaction conditions to a single intermediate at a rate that exceeds dye degradation (PDP = bis(pyridin-2-ylmethyl) bipyrrolidine; tpa = tris(2-pyridylmethyl)amine). For the less reactive [Fe(OTf)2(dpa)] (dpa = dipicolylamine), this reaction occurs on a timescale similar to that of MG oxidation. Thus, the spectroscopic method presented herein provides information about the efficiency and mechanism of iron catalyzed oxidation reactions as well as about potential oxidative catalyst decomposition and chemical changes of the catalyst before or during the oxidation reaction.

  4. Carboxymethyl cellulose coating decreases toxicity and oxidizing capacity of nanoscale zerovalent iron.

    Science.gov (United States)

    Zhou, Lei; Thanh, Thao Le; Gong, Jianyu; Kim, Jae-Hwan; Kim, Eun-Ju; Chang, Yoon-Seok

    2014-06-01

    Nanoscale zerovalent iron (NZVI) with modified surface via coating with organic stabilizers has been documented with enhanced colloidal stability and dispersity. Therefore, the expanded application potential and accompanying intrinsic exposure of such nanoparticle can be anticipated. In our study, carboxymethyl cellulose (CMC)-stabilized NZVI (CNZVI) exerted minimized oxidative stress response and slower disruption of cell membrane integrity, resulting in mitigated cytotoxicity towards bacteria Agrobacterium sp. PH-08 as compared with the uncoated counterpart. The corrosive oxidation of both nanoparticles in oxygenic water provided a better understanding of coating effect. The decreased oxidative degradation of probe 4-chlorophenol with CNZVI than NZVI implicated a weaker oxidizing capacity, which might overweight massive adhesion-mediated redox damage and explain the different exposure outcome. However, enhanced evolution of iron oxide as well as the promoted production of hydrogen peroxide adversely demonstrated CMC-coating facilitated iron corrosion by oxygen, suggesting CMC was most likely to act as a radical scavenger and compete with organics or bacteria for oxidants. Moreover, XRD, XPS and TEM results showed that the spherical NZVI was oxidized to form needle-shaped iron oxide-hydroxide (γFeOOH) with no detectable oxidative stress for PH-08, alleviating worries regarding exotoxicological impact of iron nanotechnology.

  5. Iron-dependent changes in cellular energy metabolism: influence on citric acid cycle and oxidative phosphorylation.

    Science.gov (United States)

    Oexle, H; Gnaiger, E; Weiss, G

    1999-11-10

    Iron modulates the expression of the critical citric acid cycle enzyme aconitase via a translational mechanism involving iron regulatory proteins. Thus, the present study was undertaken to investigate the consequences of iron perturbation on citric acid cycle activity, oxidative phosphorylation and mitochondrial respiration in the human cell line K-562. In agreement with previous data iron increases the activity of mitochondrial aconitase while it is reduced upon addition of the iron chelator desferrioxamine (DFO). Interestingly, iron also positively affects three other citric acid cycle enzymes, namely citrate synthase, isocitric dehydrogenase, and succinate dehydrogenase, while DFO decreases the activity of these enzymes. Consequently, iron supplementation results in increased formation of reducing equivalents (NADH) by the citric acid cycle, and thus in increased mitochondrial oxygen consumption and ATP formation via oxidative phosphorylation as shown herein. This in turn leads to downregulation of glucose utilization. In contrast, all these metabolic pathways are reduced upon iron depletion, and thus glycolysis and lactate formation are significantly increased in order to compensate for the decrease in ATP production via oxidative phosphorylation in the presence of DFO. Our results point to a complex interaction between iron homeostasis, oxygen supply and cellular energy metabolism in human cells.

  6. Freezing-Enhanced Dissolution of Iron Oxides: Effects of Inorganic Acid Anions.

    Science.gov (United States)

    Jeong, Daun; Kim, Kitae; Min, Dae Wi; Choi, Wonyong

    2015-11-03

    Dissolution of iron from mineral dust particles greatly depends upon the type and amount of copresent inorganic anions. In this study, we investigated the roles of sulfate, chloride, nitrate, and perchlorate on the dissolution of maghemite and lepidocrocite in ice under both dark and UV irradiation and compared the results with those of their aqueous counterparts. After 96 h of reaction, the total dissolved iron in ice (pH 3 before freezing) was higher than that in the aqueous phase (pH 3) by 6-28 times and 10-20 times under dark and UV irradiation, respectively. Sulfuric acid was the most efficient in producing labile iron under dark condition, whereas hydrochloric acid induced the most dissolution of the total and ferrous iron in the presence of light. This ice-induced dissolution result was also confirmed with Arizona Test Dust (AZTD). In the freeze-thaw cycling test, the iron oxide samples containing chloride, nitrate, or perchlorate showed a similar extent of total dissolved iron after each cycling while the sulfate-containing sample rapidly lost its dissolution activity with repeating the cycle. This unique phenomenon observed in ice might be related to the freeze concentration of protons, iron oxides, and inorganic anions in the liquid-like ice grain boundary region. These results suggest that the ice-enhanced dissolution of iron oxides can be a potential source of bioavailable iron, and the acid anions critically influence this process.

  7. Sulfur Versus Iron Oxidation in an Iron-Thiolate Model Complex

    Energy Technology Data Exchange (ETDEWEB)

    A McDonald; M Bukowski; E Farquhar; T Jackson; K Koehntop; M Seo; R De Hont; A Stubna; J Halfen; E Munck

    2011-12-31

    In the absence of base, the reaction of [Fe{sup II}(TMCS)]PF{sub 6} (1, TMCS = 1-(2-mercaptoethyl)-4,8,11-trimethyl-1,4,8,11-tetraazacyclotetradecane) with peracid in methanol at -20 C did not yield the oxoiron(IV) complex (2, [Fe{sup IV}(O)(TMCS)]PF{sub 6}), as previously observed in the presence of strong base (KO{sup t}Bu). Instead, the addition of 1 equiv of peracid resulted in 50% consumption of 1. The addition of a second equivalent of peracid resulted in the complete consumption of 1 and the formation of a new species 3, as monitored by UV-vis, ESI-MS, and Moessbauer spectroscopies. ESI-MS showed 3 to be formulated as [Fe{sup II}(TMCS) + 2O]{sup +}, while EXAFS analysis suggested that 3 was an O-bound iron(II)-sulfinate complex (Fe-O = 1.95 {angstrom}, Fe-S = 3.26 {angstrom}). The addition of a third equivalent of peracid resulted in the formation of yet another compound, 4, which showed electronic absorption properties typical of an oxoiron(IV) species. Moessbauer spectroscopy confirmed 4 to be a novel iron(IV) compound, different from 2, and EXAFS (Fe{double_bond}O = 1.64 {angstrom}) and resonance Raman ({nu}{sub Fe{double_bond}O} = 831 cm{sup -1}) showed that indeed an oxoiron(IV) unit had been generated in 4. Furthermore, both infrared and Raman spectroscopy gave indications that 4 contains a metal-bound sulfinate moiety ({nu}{sub s}(SO{sub 2}) {approx} 1000 cm{sup -1}, {nu}{sub as}(SO{sub 2}) {approx} 1150 cm{sup -1}). Investigations into the reactivity of 1 and 2 toward H{sup +} and oxygen atom transfer reagents have led to a mechanism for sulfur oxidation in which 2 could form even in the absence of base but is rapidly protonated to yield an oxoiron(IV) species with an uncoordinated thiol moiety that acts as both oxidant and substrate in the conversion of 2 to 3.

  8. Surface characterisation of dextran-coated iron oxide nanoparticles prepared by laser pyrolysis and coprecipitation

    Energy Technology Data Exchange (ETDEWEB)

    Carmen Bautista, M. [Instituto de Ciencia de Materiales de Madrid, CSIC, C Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Bomati-Miguel, Oscar [Instituto de Ciencia de Materiales de Madrid, CSIC, C Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Puerto Morales, Maria del [Instituto de Ciencia de Materiales de Madrid, CSIC, C Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Serna, Carlos J. [Instituto de Ciencia de Materiales de Madrid, CSIC, C Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Veintemillas-Verdaguer, Sabino [Instituto de Ciencia de Materiales de Madrid, CSIC, C Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain)]. E-mail: sabino@icmm.csic.es

    2005-05-15

    The favoured mechanism of adsorption of dextran on the surface of maghemite nanoparticles (5 nm) prepared by laser pyrolysis seems to be the collective hydrogen bonding between dextran hydroxyl groups and iron oxide particle surface. After heating, the formation of a surface complex between the polysaccharide oxygen atoms and the surface iron atoms gave rise to a stronger bonding.

  9. An autocatalytic radical chain pathway in formation of an iron(IV)-oxo complex by oxidation of an iron(II) complex with dioxygen and isopropanol.

    Science.gov (United States)

    Morimoto, Yuma; Lee, Yong-Min; Nam, Wonwoo; Fukuzumi, Shunichi

    2013-03-28

    Evidence of an autocatalytic radical chain pathway has been reported in formation of a non-heme iron(IV)-oxo complex by oxidation of an iron(II) complex with dioxygen and isopropanol in acetonitrile at 298 K. The radical chain reaction is initiated by hydrogen abstraction from isopropanol by the iron(IV)-oxo complex.

  10. Leaching of pyrite by acidophilic heterotrophic iron-oxidizing bacteria in pure and mixed cultures

    Energy Technology Data Exchange (ETDEWEB)

    Bacelar-Nicolau, P.; Johnson, D.B. [Univ. of Wales, Bangor (United Kingdom). School of Biological Sciences

    1999-02-01

    Seven strains of heterotrophic iron-oxidizing acidophilic bacteria were examined to determine their abilities to promote oxidative dissolution of pyrite (FeS{sub 2}) when they were grown in pure cultures and in mixed cultures with sulfur-oxidizing Thiobacillus spp. Only one of the isolates (strain T-24) oxidized pyrite when it was grown in pyrite-basal salts medium. However, when pyrite-containing cultures were supplemented with 0.02% (wt/vol) yeast extract, most of the isolates oxidized pyrite, and one (strain T-24) promoted rates of mineral dissolution similar to the rates observed with the iron-oxidizing autotroph Thiobacillus ferroxidans. Pyrite oxidation by another isolate (strain T-21) occurred in cultures containing between 0.005 and 0.05% (wt/vol) yeast extract but was completely inhibited in cultures containing 0.5% yeast extract. Ferrous iron was also needed for mineral dissolution by the iron-oxidizing heterotrophs, indicating that these organisms oxidize pyrite via the indirect mechanism. Mixed cultures of three isolates (strains T-21, T-232, and T-24) and the sulfur-oxidizing autotroph Thiobacillus thiooxidans promoted pyrite dissolution; since neither strains T-21 and T-23 nor T. thiooxidans could oxidize this mineral in yeast extract-free media, this was a novel example of bacterial synergism. Mixed cultures of strains T-21 and T-23 and the sulfur-oxidizing mixotroph Thiobacillus acidophilus also oxidized pyrite but to a lesser extent than did mixed cultures containing T. thiooxidans. Pyrite leaching by strain T -23 grown in an organic compound-rich medium and incubated either shaken or unshaken was also assessed. The potential environmental significance of iron-oxidizing heterotrophs in accelerating pyrite oxidation is discussed.

  11. Colloidosome-based synthesis of a multifunctional nanostructure of silver and hollow iron oxide nanoparticles

    KAUST Repository

    Pan, Yue

    2010-03-16

    Nanoparticles that self-assemble on a liquid-liquid interface serve as the building block for making heterodimeric nanostructures. Specifically, hollow iron oxide nanoparticles within hexane form colloidosomes in the aqueous solution of silver nitrate, and iron oxide exposed to the aqueous phase catalyzes the reduction of silver ions to afford a heterodimer of silver and hollow iron oxide nanoparticles. Transmission electron microscopy, selected area electron diffraction, energy-dispersive X-ray spectrometry, X-ray diffraction, UV-vis spectroscopy, and SQUID were used to characterize the heterodimers. Interestingly, the formation of silver nanoparticles helps the removal of spinglass layer on the hollow iron oxide nanoparticles. This work demonstrates a powerful yet convenient strategy for producing sophisticated, multifunctional nanostructures. © 2010 American Chemical Society.

  12. Unusual phase transition in a natural heterostructure of iron pnictides and vanadium oxides

    Science.gov (United States)

    Ok, Jong Mok; Baek, S.-H.; Eom, Man Jin; Hoch, C.; Kremer, R. K.; Kim, Dong-Hwan; Chang, Chun-Fu; Ko, Kyung-Tae; Park, Sang-Youn; Ji, Sung Dae; Büchner, B.; Park, Jae-Hoon; Shim, J. H.; Mazin, I. I.; Kim, Jun Sung

    We report the unusual phase transition in Sr2VO3FeAs single crystal, where the Mott-insulating vanadium oxides and the high-Tc superconducting iron pnictides form a natural heterostructure. Clear evidence of the phase transition at T0 = 155 K was observed in the iron pnictide layer, not in the vanadium oxide layer, using bulk and NMR measurements. Neither magnetic ordering with sufficient spin moment nor symmetry change in the crystal structure has been detected at T0. At Tmag ~ 45 K, far below T0, magnetic transition occurs in the iron pnictide layer, while the vanadium oxide layer remains nonmagnetic at low temperatures. The complex evolution of various phases in Sr2VO3FeAs is drastically distinct from the phase transitions found in other iron pnictides or vanadium oxides, highlighting the importance of the additional interlayer coupling between the layers. Equal contribution, corresponding author.

  13. One-pot size and shape controlled synthesis of DMSO capped iron oxide nanoparticles

    Indian Academy of Sciences (India)

    Debanjan Guin; Sunkara V Manorama; S Radha; A K Nigam

    2006-11-01

    We report here the capping of iron oxide nanoparticles with dimethyl sulfoxide (DMSO) to make chloroform soluble iron oxide nanoparticles. Size and shape of the capped iron oxide nanoparticles are well controlled by simply varying the reaction parameters. The synthesized nanocrystallites were characterized by thermal analysis (TG–DTA), powder X-ray diffraction (XRD), transmission electron microscopy (TEM) for evaluating phase, structure and morphology. 1H NMR spectra of the synthesized samples confirm DMSO, and the capping of DMSO on the ferrite samples. Shift of the S=O stretching frequency in Fourier transformed infrared (FTIR) spectra indicates that the bonding between DMSO and ferrite is through an oxygen moiety. The magnetic measurements of all the synthesized samples were investigated with a SQUID magnetometer which shows that the magnetic properties are strongly dependent on the size as well as shape of the iron oxide.

  14. On the electrical arc interruption by using PMMA/iron oxide nanocomposites

    Science.gov (United States)

    Doddapaneni, Venkatesh; Saleemi, Mohsin; Ye, Fei; Gati, Rudolf; Toprak, Muhammet S.

    2016-10-01

    An experimental study is undertaken on the fabrication of poly (methyl methacrylate) (PMMA)/iron oxide nanocomposites to determine their potential use for electrical arc interruption in the electrical switching applications such as circuit breakers. Monodisperse iron oxide nanoparticles of average size ∼11 nm are synthesized via thermal decomposition method and then homogeneously dispersed in the PMMA matrix by in situ polymerization. PMMA/iron oxide nanocomposites with different nanoparticle loading have been fabricated to study the effect of loading content on the thermal energy absorption. Detailed physicochemical characterizations on synthesized material are performed using x-ray powder diffraction, scanning electron microscopy, TEM, thermogravimetric analysis and differential scanning calorimetry at different processing stages. A test-setup was designed to evaluate the quality of the nanocomposites for electric arc interruption capability. The results showed that PMMA/iron oxide nanocomposites have a clear impact on the electric arc interruption and therefore should be considered as promising candidates for electrical switching applications.

  15. Magnetothermal release of payload from iron oxide/silica drug delivery agents

    Science.gov (United States)

    Luong, T. T.; Knoppe, S.; Bloemen, M.; Brullot, W.; Strobbe, R.; Locquet, J.-P.; Verbiest, T.

    2016-10-01

    The release of covalently bound Rhodamine B from iron oxide/mesoporous silica core/shell nanoparticles under magnetically induced heating was studied. The system acts as a model to study drug delivery and payload release under magnetothermal heating.

  16. Synthesizing Iron Oxide Nanostructures: The Polyethylenenemine (PEI) Role

    KAUST Repository

    Mozo, Sergio Lentijo

    2017-01-12

    Controlled synthesis of anisotropic iron oxide nanoparticles is a challenge in the field of nanomaterial research that requires an extreme attention to detail. In particular, following up a previous work showcasing the synthesis of magnetite nanorods (NRs) using a two-step approach that made use of polyethylenenemine (PEI) as a capping ligand to synthesize intermediate β-FeOOH NRs, we studied the effect and influence of the capping ligand on the formation of β-FeOOH NRs. By comparing the results reported in the literature with those we obtained from syntheses performed (1) in the absence of PEI or (2) by using PEIs with different molecular weight, we showed how the choice of different PEIs determines the aspect ratio and the structural stability of the β-FeOOH NRs and how this affects the final products. For this purpose, a combination of XRD, HRTEM, and direct current superconducting quantum interference device (DC SQUID) magnetometry was used to identify the phases formed in the final products and study their morphostructural features and related magnetic behavior.

  17. Magnetic hyperthermia in phosphate coated iron oxide nanofluids

    Science.gov (United States)

    Lahiri, B. B.; Muthukumaran, T.; Philip, John

    2016-06-01

    We study the magnetic field induced hyperthermia in water based phosphate coated Fe3O4 nanofluids, synthesized by a co-precipitation method using ferrous and ferric salt solutions, ammonia and orthophosphoric acid. The specific absorption rate (SAR) values were measured at a fixed frequency of 126 kHz and at extremely low field amplitudes. The SAR values were determined from the initial rate of temperature rise curves under non-adiabatic conditions. It was observed that the SAR initially increases with sample concentration, attains a maximum at an optimum concentration and beyond which SAR decreases. The decrease in SAR values beyond the optimum concentration was attributed to the enhancement of dipolar interaction and agglomeration of the particles. The system independent intrinsic loss power (ILP) values, obtained by normalizing the SAR values with respect to field amplitude and frequency, were found to vary between 158-125 nHm2 kg-1, which were the highest benchmark values reported in the biologically safe experimental limit of 1.03-0.92×108 Am-1 s-1. The very high value of ILP observed in the bio-compatible phosphate coated iron oxide nanofluids may find practical applications for these nanoparticles in tumor targeted hyperthermia treatment.

  18. Are iron oxide nanoparticles safe? Current knowledge and future perspectives.

    Science.gov (United States)

    Valdiglesias, Vanessa; Fernández-Bertólez, Natalia; Kiliç, Gözde; Costa, Carla; Costa, Solange; Fraga, Sonia; Bessa, Maria Joao; Pásaro, Eduardo; Teixeira, João Paulo; Laffon, Blanca

    2016-12-01

    Due to their unique physicochemical properties, including superparamagnetism, iron oxide nanoparticles (ION) have a number of interesting applications, especially in the biomedical field, that make them one of the most fascinating nanomaterials. They are used as contrast agents for magnetic resonance imaging, in targeted drug delivery, and for induced hyperthermia cancer treatments. Together with these valuable uses, concerns regarding the onset of unexpected adverse health effects following exposure have been also raised. Nevertheless, despite the numerous ION purposes being explored, currently available information on their potential toxicity is still scarce and controversial data have been reported. Although ION have traditionally been considered as biocompatible - mainly on the basis of viability tests results - influence of nanoparticle surface coating, size, or dose, and of other experimental factors such as treatment time or cell type, has been demonstrated to be important for ION in vitro toxicity manifestation. In vivo studies have shown distribution of ION to different tissues and organs, including brain after passing the blood-brain barrier; nevertheless results from acute toxicity, genotoxicity, immunotoxicity, neurotoxicity and reproductive toxicity investigations in different animal models do not provide a clear overview on ION safety yet, and epidemiological studies are almost inexistent. Much work has still to be done to fully understand how these nanomaterials interact with cellular systems and what, if any, potential adverse health consequences can derive from ION exposure.

  19. Growth and structure of nanometric iron oxide films

    Energy Technology Data Exchange (ETDEWEB)

    Guiot, E.; Gota, S.; Henriot, M.; Gautier-Soyer, M. [CEA SACLAY, Gif sur Yvette (France); Lefebvre, S. [Centre Univ. Paris Sud, Orsay (France)

    1998-12-31

    Nanometric films of iron oxides (Fe{sub 3}O{sub 4}, {alpha} and {gamma} Fe{sub 2}O{sub 3}) of high crystalline order and purity are epitaxially grown on {alpha}-Al{sub 2}O{sub 3}(0001) by atomic oxygen assisted MBE. A complete characterization of the films structure has been performed by in situ LEED and RHEED, and ex situ GIXRD using synchrotron radiation. The films grown at room temperature and post annealed at 400 C and 700 C (p{sub O{sub 2}} = 10{sup {minus}6} Torr) are respectively metastable {gamma}-Fe{sub 2}O{sub 3} (111) and {alpha}-Fe{sub 2}O{sub 3} (0001). For a substrate temperature of 450 C during growth, Fe{sub 3}O{sub 4} (111) is directly obtained. GIXRD shows an in-plane expansion of the films, which decreases with thickness (0.8 and 0.2% for film thickness of 20 and 80 {angstrom}, respectively).

  20. Iron oxide nanoparticles in modern microbiology and biotechnology.

    Science.gov (United States)

    Dinali, Ranmadugala; Ebrahiminezhad, Alireza; Manley-Harris, Merilyn; Ghasemi, Younes; Berenjian, Aydin

    2017-01-10

    Iron oxide nanoparticles (IONs) are one of the most developed and used nanomaterials in biotechnology and microbiology. These particles have unique physicochemical properties, which make them unique among nanomaterials. Therefore, many experiments have been conducted to develop facile synthesis methods for these particles and to make them biocompatible. Various effects of IONs on microorganisms have been reported. Depending on the microbial strain and nanoparticle (NP) concentration, IONs can stimulate or inhibit microbial growth. Due to the superparamagnetic properties of IONs, these NPs have used as nano sources of heat for hyperthermia in infected tissues. Antibiotic-loaded IONs are used for targeted delivery of chemical therapy direct to the infected organ and IONs have been used as a dirigible carrier for more potent antimicrobial nanomaterials such as silver nanoparticles. Magnetic NPs have been used for specific separation of pathogen and non-pathogen bacterial strains. Very recently, IONs were used as a novel tool for magnetic immobilization of microbial cells and process intensification in a biotechnological process. This review provides an overview of application of IONs in different microbial processes. Recommendations are also given for areas of future research.

  1. Iron-oxidizing microbial ecosystems thrived in late Paleoproterozoic redox-stratified oceans

    Science.gov (United States)

    Planavsky, Noah; Rouxel, Olivier; Bekker, Andrey; Shapiro, Russell; Fralick, Phil; Knudsen, Andrew

    2009-08-01

    We conducted a geochemical and petrographic study of the 1.89 billion year old Gunflint and Biwabik iron formations, with the goal of determining the importance of microbial iron-oxidation in the formation of iron- and microfossil-rich stromatolites. We used redox-sensitive tracers, such as iron isotopes and rare earth elements, to decipher whether these ancient microbial ecosystems harbored cyanobacteria or Fe-oxidizing bacteria as primary producers. Iron-rich stromatolites contain non-significant or positive Ce anomalies, which contrast with shallow water deposits having negative Ce anomalies. This trend in Ce anomalies indicates that the stromatolites formed in low oxygen conditions, which is the ideal setting for the proliferation of Fe-oxidizing bacterial ecosystems. The stromatolites yield a large range of δ 56Fe values, from -0.66 to +0.82‰, but contain predominantly positive values indicating the prevalence of partial Fe-oxidation. Based on modern analogues, Fe-oxides precipitated in cyanobacterial mats are expected to record an isotopic signature of quantitative oxidation, which in marine settings will yield negative δ 56Fe values. The stromatolite iron isotope data, therefore, provide evidence for the presence of Fe-oxidizing bacteria. The stromatolites can be traced for a distance of over 100 km in these iron formations, indicating that they record a pervasive rather than localized ecosystem. Their preservation in late Paleoproterozoic successions deposited along the margins of the Superior craton suggests that there was a global expansion of iron-oxidizing bacterial communities at shallow-water redox boundaries in late Paleoproterozoic oceans.

  2. Magnetic iron oxide nanoparticles as long wavelength photoinitiators for free radical polymerization

    OpenAIRE

    2015-01-01

    Polymer Chemistry COMMUNICATION Cite this: Polym. Chem., 2015, 6, 1918 Received 1st December 2014, Accepted 7th January 2015 DOI: 10.1039/c4py01658k www.rsc.org/polymers Magnetic iron oxide nanoparticles as long wavelength photoinitiators for free radical polymerization† Sajjad Dadashi-Silab,a Yasemin Yar,b Havva Yagci Acarb and Yusuf Yagci*a,c Iron oxide nanoparticles (Fe3O4 NPs) capped with lauric acid agents were synthesized and their photocatalyti...

  3. Magnetic tumor targeting of β-Glucosidase immobilized iron oxide nanoparticles

    OpenAIRE

    Zhou, Jie; Zhang, Jian; David, Allan E.; Yang, Victor C.

    2013-01-01

    Directed enzyme/prodrug therapy (DEPT) has promising application for cancer therapy. However, most current DEPT strategies face shortcomings such as the loss of enzyme activity during preparation, low delivery and transduction efficiency in vivo, difficult to be monitored. In current study, a novel magnetic directed enzyme/prodrug therapy (MDEPT) was set up by conjugating β-Glucosidase (β-Glu) to aminated, starch-coated, iron oxide magnetic iron oxide nanoparticles (MNP), abbreviated as β-Glu...

  4. Coupling Graphene Sheets with Iron Oxide Nanoparticles for Energy Storage and Microelectronics

    Science.gov (United States)

    2015-12-18

    AFRL-AFOSR-JP-TR-2016-0002 Coupling Graphene Sheets with Iron Oxide Nanoparticles for Energy Storage and Microelectronics Kwang-Sup Lee HANNAM...SUBTITLE Coupling Graphene Sheets with Iron Oxide Nanoparticles for Energy Storage and Microelectronics 5a. CONTRACT NUMBER FA2386-12-1-4010...Joint Project> Title “Coupling Graphene Sheets with Magnetic Nanoparticles for Energy Storage and Microelectronics ” August 13, 2015

  5. Correlation between structural and magnetic properties of sprayed iron oxide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Lobato, M.A. [Unidad Saltillo, Cinvestav, Carr. Saltillo-Monterrey Km. 13, Ramos Arizpe 25900 (Mexico); Martinez, Arturo I., E-mail: mtz.art@gmail.co [Unidad Saltillo, Cinvestav, Carr. Saltillo-Monterrey Km. 13, Ramos Arizpe 25900 (Mexico); Castro-Roman, M. [Unidad Saltillo, Cinvestav, Carr. Saltillo-Monterrey Km. 13, Ramos Arizpe 25900 (Mexico); Falcony, C. [Departamento de Fisica, Cinvestav, P.O. Box 14-7400, 7000 Mexico, DF (Mexico); Escobar-Alarcon, L. [Departamento de Fisica, Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 (Mexico)

    2011-04-01

    The structural, optical and magnetic properties of iron oxide films were investigated. Raman spectroscopy results demonstrate that different iron oxide polymorphs can coexist in the sprayed films. It also showed that thickness plays an important role in the development of mixed or pure hematite films. Among the phases detected in the films are feroxyhyte and maghemite. Additionally, the control of the magnetic properties by varying the deposition temperature and thickness is established in this work.

  6. Long circulating reduced graphene oxide-iron oxide nanoparticles for efficient tumor targeting and multimodality imaging

    Science.gov (United States)

    Xu, Cheng; Shi, Sixiang; Feng, Liangzhu; Chen, Feng; Graves, Stephen A.; Ehlerding, Emily B.; Goel, Shreya; Sun, Haiyan; England, Christopher G.; Nickles, Robert J.; Liu, Zhuang; Wang, Taihong; Cai, Weibo

    2016-06-01

    Polyethylene glycol (PEG) surface modification is one of the most widely used approaches to improve the solubility of inorganic nanoparticles, prevent their aggregation and prolong their in vivo blood circulation half-life. Herein, we developed double-PEGylated biocompatible reduced graphene oxide nanosheets anchored with iron oxide nanoparticles (RGO-IONP-1stPEG-2ndPEG). The nanoconjugates exhibited a prolonged blood circulation half-life (~27.7 h) and remarkable tumor accumulation (>11 %ID g-1) via an enhanced permeability and retention (EPR) effect. Due to the strong near-infrared absorbance and superparamagnetism of RGO-IONP-1stPEG-2ndPEG, multimodality imaging combining positron emission tomography (PET) imaging with magnetic resonance imaging (MRI) and photoacoustic (PA) imaging was successfully achieved. The promising results suggest the great potential of these nanoconjugates for multi-dimensional and more accurate tumor diagnosis and therapy in the future.

  7. Tunable room-temperature ferromagnet using an iron-oxide and graphene oxide nanocomposite

    KAUST Repository

    Lin, Aigu L.

    2015-06-23

    Magnetic materials have found wide application ranging from electronics and memories to medicine. Essential to these advances is the control of the magnetic order. To date, most room-temperature applications have a fixed magnetic moment whose orientation is manipulated for functionality. Here we demonstrate an iron-oxide and graphene oxide nanocomposite based device that acts as a tunable ferromagnet at room temperature. Not only can we tune its transition temperature in a wide range of temperatures around room temperature, but the magnetization can also be tuned from zero to 0.011 A m2/kg through an initialization process with two readily accessible knobs (magnetic field and electric current), after which the system retains its magnetic properties semi-permanently until the next initialization process. We construct a theoretical model to illustrate that this tunability originates from an indirect exchange interaction mediated by spin-imbalanced electrons inside the nanocomposite. © 2015 Scientific Reports.

  8. Electrodeposition of Polypyrrole/Reduced Graphene Oxide/Iron Oxide Nanocomposite as Supercapacitor Electrode Material

    Directory of Open Access Journals (Sweden)

    Y. C. Eeu

    2013-01-01

    Full Text Available Polypyrrole (PPy was reinforced with reduced graphene oxide (RGO and iron oxide to achieve electrochemical stability and enhancement. The ternary nanocomposite film was prepared using a facile one-pot chronoamperometry approach, which is inexpensive and experimentally friendly. The field emission scanning electron microscopy (FESEM image shows a layered morphology of the ternary nanocomposite film as opposed to the dendritic structure of PPy, suggesting hybridization of the three materials during electrodeposition. X-ray diffraction (XRD profile shows the presence of Fe2O3 in the ternary nanocomposite. Cyclic voltammetry (CV analysis illustrates enhanced current for the nanocomposite by twofold and fourfold compared to its binary (PPy/RGO and individual (PPy counterparts, respectively. The ternary nanocomposite film exhibited excellent specific capacitance retention even after 200 cycles of charge/discharge.

  9. Thrombopoietin Protects Cardiomyocytes from Iron-Overload Induced Oxidative Stress and Mitochondrial Injury

    Directory of Open Access Journals (Sweden)

    Shing Chan

    2015-07-01

    Full Text Available Background/Aims: Thalassaemia accompanied with iron-overload is common in Hong Kong. Iron-overload induced cardiomyopathy is the commonest cause of morbidity and mortality in patients with β-thalassaemia. Chronic iron-overload due to blood transfusion can cause cardiac failure. Decreased antioxidant defence and increased ROS production may lead to oxidative stress and cell injury. Iron-overload may lead to heart tissue damage through lipid peroxidation in response to oxidative stress, and a great diversity of toxic aldehydes are formed when lipid hydroperoxides break down in heart and plasma. Methods: Iron entry into embryonic heart H9C2 cells was determined by calcein assay using a fluorometer. Reactive oxygen species (ROS production in cells treated with FeCl3 or thrombopoietin (TPO was monitored by using the fluorescent probe H2DCFDA. Changes in mitochondrial membrane potential of H9C2 cells were quantified by using flow cytometry. Results: We demonstrated that iron induced oxidative stress and apoptosis in cardiomyocytes, and that iron increased ROS production and reduced cell viability in a dose-dependent manner. Iron treatment increased the proportion of cells with JC-1 monomers, indicating a trend of drop in the mitochondrial membrane potential. TPO exerted a cardio-protective effect on iron-induced apoptosis. Conclusions: These findings suggest that iron-overload leads to the generation of ROS and further induces apoptosis in cardiomyocytes via mitochondrial pathways. TPO might exert a protective effect on iron-overload induced apoptosis via inhibiting oxidative stress and suppressing the mitochondrial pathways in cardiomyocytes.

  10. Isolation of microorganisms involved in reduction of crystalline iron(III oxides in natural environments

    Directory of Open Access Journals (Sweden)

    Tomoyuki eHori

    2015-05-01

    Full Text Available Reduction of crystalline Fe(III oxides is one of the most important electron sinks for organic compound oxidation in natural environments. Yet a limited number of isolates makes it difficult to understand physiology and ecological impact of the microorganisms involved. Here, two-staged cultivation was implemented to selectively enrich and isolate crystalline iron(III reducers in soils and sediments. Firstly, iron reducers were enriched and other untargeted eutrophs were depleted by two-year successive culture on a crystalline ferric iron oxide (i.e., goethite, lepidocrocite, hematite, or magnetite as electron acceptor. Fifty-eight out of 136 incubation conditions allowed the continued existence of microorganisms as confirmed by PCR amplification. High-throughput Illumina sequencing based on 16S rRNA genes revealed that the enrichment cultures on each of the ferric iron oxides contained bacteria belonging to the Deltaproteobacteria (mainly Geobacteraceae, followed by Firmicutes and Chloroflexi, which also comprised most of the operational taxonomic units (OTUs identified. The Venn diagrams indicated that the core OTUs enriched with all of the iron oxides were dominant in the Geobacteraceae. Secondly, 38 enrichment cultures including novel microorganisms were transferred to soluble-iron(III media in order to stimulate proliferation of the enriched iron reducers. Through extinction dilution-culture and single colony isolation, six strains within the Deltaproteobacteria were finally obtained; five strains belonged to the genus Geobacter and one strain to Pelobacter. These isolates had 94.8–98.1% sequence similarities of 16S rRNA genes to cultured relatives. All the isolates were able to grow on acetate and ferric iron but their physiological characteristics differed considerably in terms of growth rate. The results demonstrate the successful enrichment and isolation of novel iron(III reducers that were able to thrive by reducing highly

  11. Synthesis of phase-pure and monodisperse iron oxide nanoparticles by thermal decomposition

    Science.gov (United States)

    Hufschmid, Ryan; Arami, Hamed; Ferguson, R. Matthew; Gonzales, Marcela; Teeman, Eric; Brush, Lucien N.; Browning, Nigel D.; Krishnan, Kannan M.

    2015-06-01

    Superparamagnetic iron oxide nanoparticles (SPIONs) are used for a wide range of biomedical applications requiring precise control over their physical and magnetic properties, which are dependent on their size and crystallographic phase. Here we present a comprehensive template for the design and synthesis of iron oxide nanoparticles with control over size, size distribution, phase, and resulting magnetic properties. We investigate critical parameters for synthesis of monodisperse SPIONs by organic thermal decomposition. Three different, commonly used, iron containing precursors (iron oleate, iron pentacarbonyl, and iron oxyhydroxide) are evaluated under a variety of synthetic conditions. We compare the suitability of these three kinetically controlled synthesis protocols, which have in common the use of iron oleate as a starting precursor or reaction intermediate, for producing nanoparticles with specific size and magnetic properties. Monodisperse particles were produced over a tunable range of sizes from approximately 2-30 nm. Reaction parameters such as precursor concentration, addition of surfactant, temperature, ramp rate, and time were adjusted to kinetically control size and size-distribution, phase, and magnetic properties. In particular, large quantities of excess surfactant (up to 25 : 1 molar ratio) alter reaction kinetics and result in larger particles with uniform size; however, there is often a trade-off between large particles and a narrow size distribution. Iron oxide phase, in addition to nanoparticle size and shape, is critical for establishing magnetic properties such as differential susceptibility (dm/dH) and anisotropy. As an example, we show the importance of obtaining the required size and iron oxide phase for application to Magnetic Particle Imaging (MPI), and describe how phase purity can be controlled. These results provide much of the information necessary to determine which iron oxide synthesis protocol is best suited to a particular

  12. Adsorption of poly(vinyl formamide-co-vinyl amine) (PVFA-co-PVAm) polymers on zinc, zinc oxide, iron, and iron oxide surfaces.

    Science.gov (United States)

    Seifert, Susan; Simon, Frank; Baumann, Giesela; Hietschold, Michael; Seifert, Andreas; Spange, Stefan

    2011-12-06

    The adsorption of poly(vinyl formamide) (PVFA) and the statistic copolymers poly(vinyl formamide-co-vinyl amine) (PVFA-co-PVAm) onto zinc and iron metal particles as well as their oxides was investigated. The adsorbates were characterized by means of XPS, DRIFT spectroscopy, wet chemical analysis, and solvatochromic probes. Dicyano-bis-(1,10-phenanthroline)-iron(II) (1), 3-(4-amino-3-methylphenyl)-7-phenyl-benzo-[1,2-b:4,5-b']difuran-2,6-dione (2), and 4-tert-butyl-2-(dicyano-methylene)-5-[4-(diethylamino)-benzylidene]-Δ(3)-thiazoline (3) as solvatochromic probes were coadsorbed onto zinc oxide to measure various effects of surface polarity. The experimental findings showed that the adsorption mechanism of PVFA and PVFA-co-PVAm strongly depends on the degree of hydrolysis of PVFA and pH values and also on the kind of metal or metal oxide surfaces that were employed as adsorbents. The adsorption mechanism of PVFA/PVFA-co-PVAm onto zinc oxide and iron oxide surfaces is mainly affected by electrostatic interactions. Particularly in the region of pH 5, the adsorption of PVFA/PVFA-co-PVAm onto zinc and iron metal particles is additionally influenced by redox processes, dissolution, and complexation reactions.

  13. Dominance of Ferritrophicum populations at an AMD site with rapid iron oxidation

    Science.gov (United States)

    Grettenberger, C.; Pearce, A.; Bibby, K. J.; Burgos, W.; Jones, D. S.; Macalady, J.

    2015-12-01

    Acid mine drainage is a major environmental problem affecting watersheds across the globe. Bioremediation of AMD relies on microbial communities to oxidize and thus remove iron from the system. Iron-oxidation rates in AMD environments are highly variable across sites. At Scalp Level Run in Summerset County PA, iron-oxidation rates are five to eight times faster than other coal-associated AMD sites. We examined the microbial community at Scalp Level Run to determine whether a unique microbial community may be responsible for the observed rapid iron-oxidation rates. Using MiSeq sequence tags, 16S rRNA gene clone libraries, and fluorescence in situ hybridization, we found that Scalp Level Run sediments host microbial populations closely related to the betaproteobacterium Ferritrophicum radicicola, an iron-oxidizing species isolated from an acid mine drainage wetland in Virginia. Ferritrophicum spp. was not found at the four other coal-associated AMD sites in the study and is uncommon in the published literature. The influence of Ferritrophicum spp. populations in biogeochemical cycling, specifically their role in determining the iron-oxidation rate at Scalp Level Run is unknown. Therefore, we employed metagenomic sequencing to examine the metabolic potential of the microbial community at Scalp Level Run.

  14. Cytotoxic Effect of Iron Oxide Nanoparticles on Mouse Embryonic Stem Cells by MTT Assay

    Directory of Open Access Journals (Sweden)

    Homa Mohseni Kouchesfehani

    2016-07-01

    Full Text Available Background: Despite the wide range of applications, there is a serious lack of information on the impact of the nanoparticles on human health and the environment. The present study was done to determine the range of dangerous concentrations of iron oxide nanoparticle and their effects on mouse embryonic stem cells. Methods: Iron oxide nanoparticles with less than 20 nanometers diameter were encapsulated by a PEG-phospholipid. The suspension of iron oxide nanoparticles was prepared using the culture media and cell viability was determined by MTT assay. Results: MTT assay was used to examine the cytotoxicity of iron oxide nanoparticle s. Royan B1 cells were treated with medium containing different concentrations (10, 20, 30, 40, 50, and 60µg/ml of the iron oxide nanoparticle. Cell viability was determined at 12 and 24 hours after treatment which showed significant decreases when concentration and time period increased. Conclusion: The main mechanism of nanoparticles action is still unknown, but in vivo and in vitro studies in different environments suggest that they are capable of producing reactive oxygen species (ROS. Therefore, they may have an effect on the concentration of intracellular calcium, activation of transcription factors, and changes in cytokine. The results of this study show that the higher concentration and duration of treatment of cells with iron oxide nanoparticles increase the rate of cell death.

  15. Iron oxide deposits associated with the ectosymbiotic bacteria in the hydrothermal vent shrimp Rimicaris exoculata

    Directory of Open Access Journals (Sweden)

    P. Compère

    2008-09-01

    Full Text Available The Rimicaris exoculata shrimp is considered as a primary consumer that dominates the fauna of most Mid-Atlantic Ridge (MAR hydrothermal ecosystems. These shrimps harbour in their gill chambers an important ectosymbiotic community of chemoautotrophic bacteria associated with iron oxide deposits. The structure and elemental composition of the mineral concretions associated with these bacteria have been investigated by using LM, ESEM, TEM STEM and EDX microanalyses. The nature of the iron oxides in shrimps obtained from the Rainbow vent field has also been determined by Mössbauer spectroscopy. This multidisciplinary approach has revealed that the three layers of mineral crust in the Rimicaris exoculata shrimps consist of large concretions formed by aggregated nanoparticles of two-line ferrihydrite and include other minor elements as Si, Ca, Mg, S and P, probably present as silicates cations, sulphates or phosphates respectively that may contribute to stabilise the ferrihydrite form of iron oxides. TEM-observations on the bacteria have revealed their close interactions with these minerals. Abiotic and biotic precipitation could occur within the gill chamber of Rimicaris exoculata, suggesting the biologically-mediated formation of the iron oxide deposits. The difference of the bacterial density in the three-mineral crust layers could be correlated to the importance of the iron oxide concretions and suggest that the first mineral particles precipitates on the lower layer which could be considered as the most likely location of iron-oxidizing bacteria.

  16. Selective catalytic oxidation of H{sub 2}S over iron oxide supported on alumina-intercalated Laponite clay catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Xin; Dou, Guangyu; Wang, Zhuo [Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); Li, Li [Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, QLD 4072 (Australia); Wang, Yufei; Wang, Hailin [Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); Hao, Zhengping, E-mail: zpinghao@rcees.ac.cn [Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China)

    2013-09-15

    Graphical abstract: The catalytic reaction and deactivation mechanisms for H{sub 2}S selective oxidation over Fe/Al-Lap catalysts are shown in the illustration. The catalytic reaction follows Mars–van Krevelen mechanism. Moreover, the interaction between iron oxide and alumina, the strong acidity of the catalysts and the well dispersion of iron oxide improve the catalytic performance efficiently. Meanwhile, the catalyst deactivation is mainly due to the formation of Fe{sub 2}(SO{sub 4}){sub 3} and elemental sulfur deposits on the surface. -- Highlights: • Fe/Al-Lap catalysts with mesoporous structure were synthesized. • Iron oxide mainly exists in form of isolate Fe{sup 3+} in an oxidic environment. •Fe/Al-Lap catalysts show high catalytic activities at low temperature. •The high catalytic activities are ascribed to the interaction between iron oxide and alumina. •The formed Fe{sub 2}(SO{sub 4}){sub 3} and elemental sulfur deposits on surface cause catalyst deactivation. -- Abstract: A series of iron oxide supported on alumina-intercalated clay catalysts (named Fe/Al-Lap catalysts) with mesoporous structure and high specific surface area were prepared. The structural and chemical properties were studied by nitrogen sorption isotherms, X-ray diffraction (XRD), UV–vis diffuse reflectance spectra (UV–vis DRS), X-ray photoelectron spectra (XPS), Fourier transform infrared spectroscopy (FTIR), H{sub 2} temperature-programmed reduction (H{sub 2}-TPR) and NH{sub 3} temperature-programmed desorption (NH{sub 3}-TPD) techniques. It was realized that iron oxide mainly existed in the form of isolated Fe{sup 3+} in an oxidic environment. Fe/Al-Lap catalysts showed high catalytic activities in the temperature range of 120–200 °C without the presence of excessive O{sub 2}. This can be attributed to the interaction between iron oxide and alumina, which improve the redox property of Fe{sup 3+} efficiently. In addition, the strong acidity of catalysts and good

  17. Selective catalytic oxidation of NO over iron and manganese oxides supported on mesoporous silica

    Institute of Scientific and Technical Information of China (English)

    Junfeng Zhang; Yan Huang; Xia Chen

    2008-01-01

    The selective catalytic oxidation (SCO)of NO was studied on a catalyst consisting of iron-manganese oxide supported on mesoporous silica (MPS) with different Mn/Fe ratios.Effects of the amount of manganese and iron,oxygen,and calcination temperature on NO conversion were also investigated.It was found that the Mn-Fe/MPS catalyst with a Mn/Fe molar ratio of l showed the highest activity at the calcination temperature of 400℃.The results showed that over this catalyst,NO conversion reached 70%under the condition of 280℃ and a space velocity of 5000 h-1.SO2 and H2O had no adverse impact on the reaction activity when the SCO reaction temperature was above 240℃.In addition,the SCO activity was suppressed gradually in the presence of SO2 and H2O below 240℃.and such an effect was reversible after heating treatment.

  18. Metal regeneration of iron chelates in nitric oxide scrubbing

    Science.gov (United States)

    Chang, S.G.; Littlejohn, D.; Shi, Y.

    1997-08-19

    The present invention relates to a process of using metal particles to reduce NO to NH{sub 3}. More specifically, the invention concerns an improved process to regenerate iron (II) (CHELATE) by reduction of iron (II) (CHELATE) (NO) complex, which process comprises: (a) contacting an aqueous solution containing iron (II) (CHELATE) (NO) with metal particles at between about 20 and 90 C to reduce NO present, produce ammonia or an ammonium ion, and produce free iron (II) (CHELATE) at a pH of between about 3 and 8. The process is useful to remove NO from flue gas and reduce pollution. 34 figs.

  19. Mineral and iron oxidation at low temperatures by pure and mixed cultures of acidophilic microorganisms.

    Science.gov (United States)

    Dopson, Mark; Halinen, Anna-Kaisa; Rahunen, Nelli; Ozkaya, Bestamin; Sahinkaya, Erkan; Kaksonen, Anna H; Lindström, E Börje; Puhakka, Jaakko A

    2007-08-01

    An enrichment culture from a boreal sulfide mine environment containing a low-grade polymetallic ore was tested in column bioreactors for simulation of low temperature heap leaching. PCR-denaturing gradient gel electrophoresis and 16S rRNA gene sequencing revealed the enrichment culture contained an Acidithiobacillus ferrooxidans strain with high 16S rRNA gene similarity to the psychrotolerant strain SS3 and a mesophilic Leptospirillum ferrooxidans strain. As the mixed culture contained a strain that was within a clade with SS3, we used the SS3 pure culture to compare leaching rates with the At. ferrooxidans type strain in stirred tank reactors for mineral sulfide dissolution at various temperatures. The psychrotolerant strain SS3 catalyzed pyrite, pyrite/arsenopyrite, and chalcopyrite concentrate leaching. The rates were lower at 5 degrees C than at 30 degrees C, despite that all the available iron was in the oxidized form in the presence of At. ferrooxidans SS3. This suggests that although efficient At. ferrooxidans SS3 mediated biological oxidation of ferrous iron occurred, chemical oxidation of the sulfide minerals by ferric iron was rate limiting. In the column reactors, the leaching rates were much less affected by low temperatures than in the stirred tank reactors. A factor for the relatively high rates of mineral oxidation at 7 degrees C is that ferric iron remained in the soluble phase whereas, at 21 degrees C the ferric iron precipitated. Temperature gradient analysis of ferrous iron oxidation by this enrichment culture demonstrated two temperature optima for ferrous iron oxidation and that the mixed culture was capable of ferrous iron oxidation at 5 degrees C.

  20. Iron chelators can protect against oxidative stress through ferryl heme reduction.

    Science.gov (United States)

    Reeder, Brandon J; Hider, Robert C; Wilson, Michael T

    2008-02-01

    Iron chelators such as desferrioxamine have been shown to ameliorate oxidative damage in vivo. The mechanism of this therapeutic action under non-iron-overload conditions is, however, complex, as desferrioxamine has properties that can impact on oxidative damage independent of its capacity to act as an iron chelator. Desferrioxamine can act as a reducing agent to remove cytotoxic ferryl myoglobin and hemoglobin and has recently been shown to prevent the formation of a highly cytotoxic heme-to-protein cross-linked derivative of myoglobin. In this study we have examined the effects of a wide range of iron chelators, including the clinically used hydroxypyridinone CP20 (deferriprone), on the stability of ferryl myoglobin and on the formation of heme-to-protein cross-linking. We show that all hydroxypyridinones, as well as many other iron chelators, are efficient reducing agents of ferryl myoglobin. These compounds are also effective at preventing the formation of cytotoxic derivatives of myoglobin such as heme-to-protein cross-linking. These results show that the use of iron chelators in vivo may ameliorate oxidative damage under conditions of non-iron overload by at least two mechanisms. The antioxidant effects of chelators in vivo cannot, therefore, be attributed solely to iron chelation.

  1. Indefinitely stable iron(IV) cage complexes formed in water by air oxidation

    Science.gov (United States)

    Tomyn, Stefania; Shylin, Sergii I.; Bykov, Dmytro; Ksenofontov, Vadim; Gumienna-Kontecka, Elzbieta; Bon, Volodymyr; Fritsky, Igor O.

    2017-01-01

    In nature, iron, the fourth most abundant element of the Earth's crust, occurs in its stable forms either as the native metal or in its compounds in the +2 or +3 (low-valent) oxidation states. High-valent iron (+4, +5, +6) compounds are not formed spontaneously at ambient conditions, and the ones obtained synthetically appear to be unstable in polar organic solvents, especially aqueous solutions, and this is what limits their studies and use. Here we describe unprecedented iron(IV) hexahydrazide clathrochelate complexes that are assembled in alkaline aqueous media from iron(III) salts, oxalodihydrazide and formaldehyde in the course of a metal-templated reaction accompanied by air oxidation. The complexes can exist indefinitely at ambient conditions without any sign of decomposition in water, nonaqueous solutions and in the solid state. We anticipate that our findings may open a way to aqueous solution and polynuclear high-valent iron chemistry that remains underexplored and presents an important challenge.

  2. Heterogeneous biomimetic catalysis using iron porphyrin for cyclohexane oxidation promoted by chitosan

    Science.gov (United States)

    Huang, Guan; Liu, Yao; Cai, Jing Li; Chen, Xiang Feng; Zhao, Shu Kai; Guo, Yong An; Wei, Su Juan; Li, Xu

    2017-04-01

    This study investigates how ligands modulate metalloporphyrin activity with the goal of producing a practical biomimetic catalyst for use in the chemical industry. We immobilized iron porphyrinate [iron-tetrakis-(4-sulfonatophenyl)-porphyrin; Fe(III) (TPPS)] on powdered chitosan (pd-CTS) to form an immobilized catalyst Fe(III) (TPPS)/pd-CTS, which was characterized using modern spectroscopic techniques and used for catalytic oxidation of cyclohexane with O2. Amino coordination to iron porphyrin in Fe(III) (TPPS)/pd-CTS altered the electron cloud density around the iron cation, probably by reducing the activation energy of Fe(III) (TPPS) and raising the reactivity of the iron ion catalytic center, thereby improving the catalytic efficiency. One milligram of Fe(III) (TPPS) catalyst can be reused three times for the oxidation reaction to yield an average of 22.9 mol% of cyclohexanone and cyclohexanol.

  3. Interactions of proteins with biogenic iron oxyhydroxides and a new culturing technique to increase biomass yields of neutrophilic, iron-oxidizing bacteria.

    Science.gov (United States)

    Barco, Roman A; Edwards, Katrina J

    2014-01-01

    Neutrophilic, bacterial iron-oxidation remains one of the least understood energy-generating biological reactions to date. One of the reasons it remains under-studied is because there are inherent problems with working with iron-oxidizing bacteria (FeOB), including low biomass yields and interference from the iron oxides in the samples. In an effort to circumvent the problem of low biomass, a new large batch culturing technique was developed. Protein interactions with biogenic iron oxides were investigated confirming that such interactions are strong. Therefore, a protein extraction method is described to minimize binding of proteins to biogenic iron oxides. The combination of these two methods results in protein yields that are appropriate for activity assays in gels and for proteomic profiling.

  4. Iron

    Science.gov (United States)

    Iron is a mineral that our bodies need for many functions. For example, iron is part of hemoglobin, a protein which carries ... It helps our muscles store and use oxygen. Iron is also part of many other proteins and ...

  5. Iron

    Science.gov (United States)

    ... of iron stored in the body become low, iron deficiency anemia sets in. Red blood cells become smaller and ... from the lungs throughout the body. Symptoms of iron deficiency anemia include tiredness and lack of energy, GI upset, ...

  6. Role of descriptors in predicting the dissolution energy of embedded oxides and the bulk modulus of oxide-embedded iron

    Science.gov (United States)

    Takahashi, Keisuke; Tanaka, Yuzuru

    2017-01-01

    Oxide-embedded bulk iron is investigated in terms of first principles calculations and data mining. Twenty-nine oxides are embedded into a vacancy site of iron where first principles calculations are performed and the resulting calculations are stored as a data set. A prediction of the dissolution energy of oxides within iron and the bulk modulus of oxide-embedded iron is performed using machine learning. In particular, support vector machine (SVM) and linear regression (LR) are implemented where descriptors for determining the dissolution energy and bulk modulus are revealed. With trained SVM and LR, the prediction of the dissolution energy for different oxides in iron and the inverse problem—deriving the corresponding descriptor variables from a desired bulk modulus—are achieved. The physical origin behind the chosen descriptors is also revealed where manipulating each individual descriptor within a multidimensional space allows for the prediction of the dissolution energy and bulk modulus. Thus, predictions of physical phenomena are, in principle, achievable if the appropriate descriptors are determined.

  7. Iron oxidation and biomineralization by Mariprofundus ferrooxydans, a deep-sea microaerophilic lithoautotroph

    Science.gov (United States)

    Chan, C. S.; Emerson, D.; Fakra, S.; Edwards, K. J.

    2007-12-01

    The ocean crust contains a large reservoir of reduced iron, available for microbial energy generation. Some of this ferrous iron is mobilized by fluids in hydrothermal fields at seamounts and mid-ocean ridges. A microaerophilic iron oxidizer, Mariprofundus ferrooxydans has been identified (by molecular methods and microscopy) at various sites, and appears to be a key iron-oxidizing bacterium (FeOB) in the deep sea. Originally isolated from microbial mats near vents at the Loihi Seamount in Hawaii, Mariprofundus is distinctive because it forms an extracellular iron-mineralized stalk-like structure. We aim to understand its metabolism and mineral formation using a multidisciplinary approach, including electron microscopy, x-ray spectroscopy, time-lapse light microscopic imaging of live cells, and genomic and biochemical analyses. Microscopy and spectroscopy work shows that as the cells grow, they excretes iron and organic-rich fibrils that make up the stalk, at a rate of ~2 microns/hr. Stalk growth appears to be parallel to the direction of Fe and oxygen gradients. The Mariprofundus genome contains several terminal oxidases/peroxidases, including two cbb3-type cytochrome oxidases with a high affinity for oxygen, consistent with the microaerophilic lifestyle of these organisms. However, we have not identified genes for metabolisms other than aerobic iron oxidation, nor have we found any genes similar to known or suspected iron oxidases, though the genome (2.87 Mb) is rich in cytochromes (32 of 2922 genes). Thus, we are performing experiments to extract and analyze proteins from both cultured and environmental samples in order to find ones that will oxidize iron. UV-Vis spectra of extracts suggest that c-type cytochromes are particularly abundant, so these are candidates for further investigation. In combination with the microscopy and spectroscopy studies, these are the first steps towards understanding the complete pathway of iron from uptake through mineral

  8. Iron metabolism and oxidative profile of dogs naturally infected by Ehrlichia canis: Acute and subclinical disease.

    Science.gov (United States)

    Bottari, Nathieli B; Crivellenti, Leandro Z; Borin-Crivellenti, Sofia; Oliveira, Jéssica R; Coelho, Stefanie B; Contin, Catarina M; Tatsch, Etiane; Moresco, Rafael N; Santana, Aureo E; Tonin, Alexandre A; Tinucci-Costa, Mirela; Da Silva, Aleksandro S

    2016-03-01

    The aim of this study was to evaluate the oxidant profile and iron metabolism in serum of dogs infected by Ehrlichia canis. Banked sera samples of dogs were divided into two groups: negative control (n = 17) and infected by E. canis on acute (n = 24), and subclinical (n = 18) phases of the disease. The eritrogram, leucogram, and platelet counts were evaluate as well as iron, ferritin, and transferrin levels, latent iron binding capacity (LIBC), and transferrin saturation index (TSI) concentration. In addition, the advanced oxidation protein products (AOPP) and ferric reducing ability of plasma (FRAP) in sera were also analyzed. Blood samples were examined for the presence of E. canis by PCR techniques. History and clinical signals were recorded for each dog. During the acute phase of the disease, infected animals showed thrombocytopenia and anemia when compared to healthy animals (P canis showed changes in the iron metabolism and developed an oxidant status in consequence of disease pathophysiology.

  9. N-butylamine functionalized graphene oxide for detection of iron(III) by photoluminescence quenching.

    Science.gov (United States)

    Gholami, Javad; Manteghian, Mehrdad; Badiei, Alireza; Ueda, Hiroshi; Javanbakht, Mehran

    2016-02-01

    An N-butylamine functionalized graphene oxide nanolayer was synthesized and characterized by ultraviolet (UV)-visible spectrometry, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and transmission electron microscopy. Detection of iron(III) based on photoluminescence spectroscopy was investigated. The N-butylamine functionalized graphene oxide was shown to specifically interact with iron (III), compared with other cationic trace elements including potassium (I), sodium (I), calcium (II), chromium (III), zinc (II), cobalt (II), copper (II), magnesium (II), manganese (II), and molybdenum (VI). The quenching effect of iron (III) on the luminescence emission of N-butylamine functionalized graphene oxide layer was used to detect iron (III). The limit of detection (2.8 × 10(-6)  M) and limit of quantitation (2.9 × 10(-5)  M) were obtained under optimal conditions.

  10. Shape control of the magnetic iron oxide nanoparticles under different chain length of reducing agents

    Energy Technology Data Exchange (ETDEWEB)

    Ngoi, Kuan Hoon; Chia, Chin-Hua, E-mail: chia@ukm.edu.my; Zakaria, Sarani [School of Applied Physics, Faculty Science and Technology, University Kebangsaan Malaysia 43600 UKM Bangi, Selangor (Malaysia); Chiu, Wee Siong [Low Dimensional Materials Research Centre, Department of Physics, Faculty of Science, University of Malaya, 50603 Lembah Pantai, Kuala Lumpur (Malaysia)

    2015-09-25

    We report on the effect of using reducing agents with different chain-length on the synthesis of iron oxide nanoparticles by thermal decomposition of iron (III) acetylacetonate in 1-octadecene. This modification allows us to control the shape of nanoparticles into spherical and cubic iron oxide nanoparticles. The highly monodisperse 14 nm spherical nanoparticles are obtained under 1,2-dodecanediol and average 14 nm edge-length cubic iron oxide nanoparticles are obtained under 1,2-tetradecanediol. The structural characterization such as transmission electron microscope (TEM) and X-ray diffraction (XRD) shows similar properties between two particles with different shapes. The vibrating sample magnetometer (VSM) shows no significant difference between spherical and cubic nanoparticles, which are 36 emu/g and 37 emu/g respectively and superparamagnetic in nature.

  11. Cell adhesion of Shewanella oneidensis to iron oxide minerals: Effect of different single crystal faces

    Directory of Open Access Journals (Sweden)

    Hochella Michael F

    2005-12-01

    Full Text Available The results of experiments designed to test the hypothesis that near-surface molecular structure of iron oxide minerals influences adhesion of dissimilatory iron reducing bacteria are presented. These experiments involved the measurement, using atomic force microscopy, of interaction forces generated between Shewanella oneidensis MR-1 cells and single crystal growth faces of iron oxide minerals. Significantly different adhesive force was measured between cells and the (001 face of hematite, and the (100 and (111 faces of magnetite. A role for electrostatic interactions is apparent. The trend in relative forces of adhesion generated at the mineral surfaces is in agreement with predicted ferric site densities published previously. These results suggest that near-surface structure does indeed influence initial cell attachment to iron oxide surfaces; whether this is mediated via specific cell surface-mineral surface interactions or by more general interfacial phenomena remains untested.

  12. Mutual effects of nitric oxide and iron on the growth of marine algae

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    Experiments on the effects of nitric oxide (NO) and iron on the growth of marine microalgae Skeletonema costatum were conducted.The results are as follows: exogenous NO could increase the growth rate of marine algae and raise the biomass remarkably under iron-deficient conditions. But it was a complicated process that the phytoplankton growth was influenced by NO and iron, which was controlled by the NO concentration, the nutrition level of the culture medium and the iron concentration, etc. Meanwhile, the iron concentration in the medium also has a direct influence on the growth and NO release capacity of the algae. Therefore, the effects of NO and iron on the growth of marine phytoplankton were mutual.

  13. Magnetic iron oxides in the cementation technology of the boron-containing radioactive waste

    Science.gov (United States)

    Fedotov, M. A.; Gorbunova, O. A.; Fedorova, O. V.; Folmanis, G. E.; Kovalenko, L. V.

    2015-04-01

    Two ways of synthesis of non-detachable dispersed particles of magnetic materials useful for the boron-containing waste cementation process regulation were developed. Powder XRD showed that the method of carbothermic recovery of nanoscale iron hydroxide allows obtaining a mixture of iron oxides with content of the magnetic phase up to 70%. Method of low-temperature hydrogen reduction of the raw materials allows obtaining various compositions of a-iron and iron oxides with the possibility to change the size of the final particles in a wide range. The possibility of using composites of magnetic iron oxides and metal oxide compositions instead of ferromagnetic rods with VEP of boron-containing liquid radioactive waste in the fluidized field was studied. It was shown that the use of fine and nano particles of the iron oxides in the pre-treatment of the boron-containing LRW increases the strength of the final compounds and accelerates the cement setting compounds from 13 to 5-9 days.

  14. Production and characterization of the nanostructured hollow iron oxide spheres and nanoparticles by aerosol route

    Energy Technology Data Exchange (ETDEWEB)

    Gurmen, Sebahattin, E-mail: gurmen@itu.edu.t [Metallurgical and Materials Eng. Dept., Istanbul Technical University, 34469 Istanbul (Turkey); Ebin, Burcak [Metallurgical and Materials Eng. Dept., Istanbul Technical University, 34469 Istanbul (Turkey)

    2010-03-04

    Nanoshell hollow iron oxide ({alpha}-Fe{sub 2}O{sub 3}) spheres and nanoparticles were produced by ultrasonic spray pyrolysis (USP) method from iron(III) chloride salts. Iron oxide nanostructures were obtained by thermal decomposition of aerosol formed in the ultrasonic generator from aqueous solution of FeCl{sub 3} as a precursor. Hollow structure of iron oxide particles was controlled by reaction temperature changing between 600 and 200 {sup o}C and with the addition of the polyethylene glycol (PEG) iron oxide nanoparticles were fabricated. X-ray diffraction (XRD) studies and Scherrer crystalline size calculations show that the crystal sizes of the nanostructured iron oxide were between 33 and 18 nm. Energy dispersive spectroscopy (EDS) was performed to determine the chemical composition of the particles. Scanning electron microscope (SEM) investigation gave detailed information about particle size and morphology. Transmission electron microscope (TEM) was used to confirm the hollow structure of the particles and identify the thickness of the shell.

  15. Ultrasonic computed tomography imaging of iron oxide nanoparticles

    Science.gov (United States)

    Perlman, Or; Azhari, Haim

    2017-02-01

    Iron oxide nanoparticles (IONPs) are becoming increasingly used and intensively investigated in the field of medical imaging. They are currently FDA approved for magnetic resonance imaging (MRI), and it would be highly desirable to visualize them by ultrasound as well. Previous reports using the conventional ultrasound B-scan (pulse-echo) imaging technique have shown very limited detectability of these particles. The aim of this study is to explore the feasibility of imaging IONPs using the through-transmission ultrasound methodology and demonstrate their detectability using ultrasonic computed tomography (UCT). Commercially available IONPs were acoustically analysed to quantify their effect on the speed of sound (SOS) and acoustic attenuation as a function of concentration. Next, through-transmission projection and UCT imaging were performed on a breast mimicking phantom and on an ex vivo tissue model, to which IONPs were injected. Finally, an MRI scan was performed to verify that the same particles examined in the ultrasound experiment can be imaged by magnetic resonance, using the same clinically relevant concentrations. The results have shown a consistent concentration dependent speed of sound increase (1.86 \\text{m}{{\\text{s}}^{-1}} rise per 100 µg · ml-1 IONPs). Imaging based on this property has shown a substantial contrast-to-noise ratio improvement (up to 5 fold, p  image contrast and allowed the detection of the particles existence and location, in both raster-scan projection and UCT imaging. Conversely, no significant change in the acoustic attenuation coefficient was noted. Based on these findings, it is concluded that IONPs can be used as an effective SOS-based contrast agent, potentially useful for ultrasonic breast imaging. Furthermore, the particle offers the capacity of significantly enhancing diagnosis accuracy using multimodal MRI-ultrasound imaging capabilities.

  16. The responses of immune cells to iron oxide nanoparticles.

    Science.gov (United States)

    Xu, Yaolin; Sherwood, Jennifer A; Lackey, Kimberly H; Qin, Ying; Bao, Yuping

    2016-04-01

    Immune cells play an important role in recognizing and removing foreign objects, such as nanoparticles. Among various parameters, surface coatings of nanoparticles are the first contact with biological system, which critically affect nanoparticle interactions. Here, surface coating effects on nanoparticle cellular uptake, toxicity and ability to trigger immune response were evaluated on a human monocyte cell line using iron oxide nanoparticles. The cells were treated with nanoparticles of three types of coatings (negatively charged polyacrylic acid, positively charged polyethylenimine and neutral polyethylene glycol). The cells were treated at various nanoparticle concentrations (5, 10, 20, 30, 50 μg ml(-1) or 2, 4, 8, 12, 20 μg cm(-2)) with 6 h incubation or treated at a nanoparticle concentration of 50 μg ml(-1) (20 μg cm(-2)) at different incubation times (6, 12, 24, 48 or 72 h). Cell viability over 80% was observed for all nanoparticle treatment experiments, regardless of surface coatings, nanoparticle concentrations and incubation times. The much lower cell viability for cells treated with free ligands (e.g. ~10% for polyethylenimine) suggested that the surface coatings were tightly attached to the nanoparticle surfaces. The immune responses of cells to nanoparticles were evaluated by quantifying the expression of toll-like receptor 2 and tumor necrosis factor-α. The expression of tumor necrosis factor-α and toll-like receptor 2 were not significant in any case of the surface coatings, nanoparticle concentrations and incubation times. These results provide useful information to select nanoparticle surface coatings for biological and biomedical applications.

  17. Magnetic field calculations for iron oxide nanoparticles for MRI

    Science.gov (United States)

    Hernandez, Ricardo; Mendez Rojas, Miguel; Dies Suarez, Pilar; Hidalgo Tobón, Silvia

    2014-11-01

    The susceptibility effects of superparamagnetic iron oxide nanoparticles (SPIONs) functionalized with triethylenglycol (TREG) and Polyethylen Glycol (PEG) has been studied, those nanoparticles have the necessary properties to be used in the clinic as contrast media in imaging by MRI[1-3]. We are considering the behavior of the magnetic field as plane wave to explain the electrical and magnetic field produced by SPIONs. Images were acquired on a 1.5T imager Philips, using mFFE Sequence. Three glass capillary tubes with a) TREG (10nm) concentration of 300 μg/ml, and PEGCOOH 6000(10nm) with 300 μg/ml, and 2% agarosa. Magnetic field simulations were calculated in Matlab. The plane wave that comes in contact with a sphere of radius a, an propagation constant k1, and it is in an homogeneous space k2. We consider that the electric field is linearly polarized on x-direction, with a propagation on z-positive-axis. The secondary induced field can be explained from the interior of the sphere and valid exterior points. The referred waves are transmitted and reflected, this is valid only when the wavelength is smaller than the radius of the sphere. The obtained vibrational mode is an answer of the electrical oscillation and this is projection of the disturbed magnetic field. TREG-SPIONs produce more serious susceptibility artefacts compared to PEG-SPIONs. This study is promissory due to the concordance of the results of the simulations and the inhomogeneities showed in the MR images.

  18. Effect of iron oxide loading on the phase transformation and physicochemical properties of nanosized mesoporous ZrO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Basahel, S.N. [Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, 21589 Jeddah (Saudi Arabia); Ali, Tarek T. [Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, 21589 Jeddah (Saudi Arabia); Chemistry Department, Faculty of Science, Sohag University, 82524 Sohag (Egypt); Narasimharao, K. [Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, 21589 Jeddah (Saudi Arabia); Bagabas, A.A. [Petrochemicals Research Institute (PRI), King Abdulaziz City for Science and Technology (KACST), P.O. Box 6086, 11442 Riyadh (Saudi Arabia); Mokhtar, M., E-mail: mmokhtar2000@yahoo.com [Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, 21589 Jeddah (Saudi Arabia)

    2012-11-15

    Highlights: ► Modified preparation method for nanosized iron oxide supported ZrO{sub 2} catalysts. ► Systematic study of effect of high iron oxide loading over ZrO{sub 2}. ► Influence of iron oxide on the stabilization of tetragonal ZrO{sub 2} phase. ► A mesoporous nature of zirconia changed upon changing iron oxide loading. ► Surface to bulk migration of iron oxide evidenced by XPS technique. -- Abstract: Mesoporous ZrO{sub 2}-supported iron oxide materials were prepared with nominal loadings of iron oxide of 5, 10, 15 and 20 wt.% using a modified co-precipitation method. The physicochemical properties of the catalysts were characterized by thermogravimetric analysis, differential scanning calorimetry, X-ray diffraction, Raman spectroscopy, high resolution transmission electron microscopy, N{sub 2} adsorption, X-ray photoelectron spectroscopy and infrared spectroscopy methods. A delay in the ZrO{sub 2} phase transformation as a result of the incorporation of iron was determined using TG/DSC measurements. XRD, Raman spectroscopy and HRTEM results revealed that an increase of iron oxide loading from 5 to 15 wt.% enhanced the transformation of the monoclinic to tetragonal phase. Unexpectedly, 20 wt.% iron oxide loading was required for complete tetragonal structure stabilization due to the mesoporosity of the ZrO{sub 2} support. Iron oxide loadings from 5 to 15 wt.% showed an increase in the BET-surface area due to the presence of amorphous iron oxide on the surface. XPS and FTIR results indicated that increasing the iron oxide content to 20 wt.% resulted in stabilization of the tetragonal zirconia phase as a result of surface-to-bulk migration and incorporation of Fe{sup 3+} ions in the ZrO{sub 2} lattice.

  19. Water oxidation catalysis with nonheme iron complexes under acidic and basic conditions: homogeneous or heterogeneous?

    Science.gov (United States)

    Hong, Dachao; Mandal, Sukanta; Yamada, Yusuke; Lee, Yong-Min; Nam, Wonwoo; Llobet, Antoni; Fukuzumi, Shunichi

    2013-08-19

    Thermal water oxidation by cerium(IV) ammonium nitrate (CAN) was catalyzed by nonheme iron complexes, such as Fe(BQEN)(OTf)2 (1) and Fe(BQCN)(OTf)2 (2) (BQEN = N,N'-dimethyl-N,N'-bis(8-quinolyl)ethane-1,2-diamine, BQCN = N,N'-dimethyl-N,N'-bis(8-quinolyl)cyclohexanediamine, OTf = CF3SO3(-)) in a nonbuffered aqueous solution; turnover numbers of 80 ± 10 and 20 ± 5 were obtained in the O2 evolution reaction by 1 and 2, respectively. The ligand dissociation of the iron complexes was observed under acidic conditions, and the dissociated ligands were oxidized by CAN to yield CO2. We also observed that 1 was converted to an iron(IV)-oxo complex during the water oxidation in competition with the ligand oxidation. In addition, oxygen exchange between the iron(IV)-oxo complex and H2(18)O was found to occur at a much faster rate than the oxygen evolution. These results indicate that the iron complexes act as the true homogeneous catalyst for water oxidation by CAN at low pHs. In contrast, light-driven water oxidation using [Ru(bpy)3](2+) (bpy = 2,2'-bipyridine) as a photosensitizer and S2O8(2-) as a sacrificial electron acceptor was catalyzed by iron hydroxide nanoparticles derived from the iron complexes under basic conditions as the result of the ligand dissociation. In a buffer solution (initial pH 9.0) formation of the iron hydroxide nanoparticles with a size of around 100 nm at the end of the reaction was monitored by dynamic light scattering (DLS) in situ and characterized by X-ray photoelectron spectra (XPS) and transmission electron microscope (TEM) measurements. We thus conclude that the water oxidation by CAN was catalyzed by short-lived homogeneous iron complexes under acidic conditions, whereas iron hydroxide nanoparticles derived from iron complexes act as a heterogeneous catalyst in the light-driven water oxidation reaction under basic conditions.

  20. Discovery of Fe7O9: a new iron oxide with a complex monoclinic structure

    Science.gov (United States)

    Sinmyo, Ryosuke; Bykova, Elena; Ovsyannikov, Sergey V.; McCammon, Catherine; Kupenko, Ilya; Ismailova, Leyla; Dubrovinsky, Leonid

    2016-09-01

    Iron oxides are fundamentally important compounds for basic and applied sciences as well as in numerous industrial applications. In this work we report the synthesis and investigation of a new binary iron oxide with the hitherto unknown stoichiometry of Fe7O9. This new oxide was synthesized at high-pressure high-temperature (HP-HT) conditions, and its black single crystals were successfully recovered at ambient conditions. By means of single crystal X-ray diffraction we determined that Fe7O9 adopts a monoclinic C2/m lattice with the most distorted crystal structure among the binary iron oxides known to date. The synthesis of Fe7O9 opens a new portal to exotic iron-rich (M,Fe)7O9 oxides with unusual stoichiometry and distorted crystal structures. Moreover, the crystal structure and phase relations of such new iron oxide groups may provide new insight into the cycling of volatiles in the Earth’s interior.

  1. Selective catalytic oxidation of H₂S over iron oxide supported on alumina-intercalated Laponite clay catalysts.

    Science.gov (United States)

    Zhang, Xin; Dou, Guangyu; Wang, Zhuo; Li, Li; Wang, Yufei; Wang, Hailin; Hao, Zhengping

    2013-09-15

    A series of iron oxide supported on alumina-intercalated clay catalysts (named Fe/Al-Lap catalysts) with mesoporous structure and high specific surface area were prepared. The structural and chemical properties were studied by nitrogen sorption isotherms, X-ray diffraction (XRD), UV-vis diffuse reflectance spectra (UV-vis DRS), X-ray photoelectron spectra (XPS), Fourier transform infrared spectroscopy (FTIR), H₂ temperature-programmed reduction (H₂-TPR) and NH₃ temperature-programmed desorption (NH3-TPD) techniques. It was realized that iron oxide mainly existed in the form of isolated Fe(3+) in an oxidic environment. Fe/Al-Lap catalysts showed high catalytic activities in the temperature range of 120-200 °C without the presence of excessive O₂. This can be attributed to the interaction between iron oxide and alumina, which improve the redox property of Fe(3+) efficiently. In addition, the strong acidity of catalysts and good dispersion of iron oxide were also beneficial to oxidation reaction. Among them, 7% Fe/Al-Lap catalyst presented the best catalytic performance at 180 °C. Finally, the catalytic and deactivation mechanisms were explored.

  2. Oxidative Profile and δ-Aminolevulinate Dehydratase Activity in Healthy Pregnant Women with Iron Supplementation.

    Science.gov (United States)

    De Lucca, Leidiane; Rodrigues, Fabiane; Jantsch, Letícia B; Neme, Walter S; Gallarreta, Francisco M P; Gonçalves, Thissiane L

    2016-05-03

    An oxidative burst occurs during pregnancy due to the large consumption of oxygen in the tissues and an increase in metabolic demands in response to maternal physiological changes and fetal growth. This study aimed to determine the oxidative profile and activity of δ-aminolevulinate dehydratase (δ-ALA-D) in pregnant women who received iron supplementation. Oxidative stress parameters were evaluated in 25 pregnant women with iron supplementation, 25 pregnant women without supplementation and 25 non-pregnant women. The following oxidative stress parameters were evaluated: thiobarbituric acid reactive substances (TBARS), protein thiol groups (P-SH), non-protein thiol levels (NP-SH), vitamin C levels, catalase and δ-ALA-D activity. Markers of oxidative stress and cell damage, such as TBARS in plasma were significantly higher in pregnant women without supplementation. Levels of P-SH, NP-SH and δ-ALA-D activity were significantly lower in pregnant women without supplementation compared to non-pregnant and pregnant women with supplementation, while vitamin C levels were significantly lower in pregnant women without supplementation when compared to non-pregnant women. The increase in the generation of oxidative species and decrease of antioxidants suggest the loss of physiological oxidative balance during normal pregnancy, which was not observed in pregnant women with iron supplementation, suggesting a protective effect of iron against oxidative damage.

  3. Iron-oxide-supported nanocarbon in lithium-ion batteries, medical, catalytic, and environmental applications.

    Science.gov (United States)

    Tuček, Jiří; Kemp, Kingsley Christian; Kim, Kwang Soo; Zbořil, Radek

    2014-08-26

    Owing to the three different orbital hybridizations carbon can adopt, the existence of various carbon nanoallotropes differing also in dimensionality has been already affirmed with other structures predicted and expected to emerge in the future. Despite numerous unique features and applications of 2D graphene, 1D carbon nanotubes, or 0D fullerenes, nanodiamonds, and carbon quantum dots, which have been already heavily explored, any of the existing carbon allotropes do not offer competitive magnetic properties. For challenging applications, carbon nanoallotropes are functionalized with magnetic species, especially of iron oxide nature, due to their interesting magnetic properties (superparamagnetism and strong magnetic response under external magnetic fields), easy availability, biocompatibility, and low cost. In addition, combination of iron oxides (magnetite, maghemite, hematite) and carbon nanostructures brings enhanced electrochemical performance and (photo)catalytic capability due to synergetic and cooperative effects. This work aims at reviewing these advanced applications of iron-oxide-supported nanocarbon composites where iron oxides play a diverse role. Various architectures of carbon/iron oxide nanocomposites, their synthetic procedures, physicochemical properties, and applications are discussed in details. A special attention is devoted to hybrids of carbon nanotubes and rare forms (mesoporous carbon, nanofoam) with magnetic iron oxide carriers for advanced environmental technologies. The review also covers the huge application potential of graphene/iron oxide nanocomposites in the field of energy storage, biomedicine, and remediation of environment. Among various discussed medical applications, magnetic composites of zero-dimensional fullerenes and carbon dots are emphasized as promising candidates for complex theranostics and dual magneto-fluorescence imaging.

  4. Discovery of Fe7O9: a new iron oxide with a complex monoclinic structure

    OpenAIRE

    Ryosuke Sinmyo; Elena Bykova; Ovsyannikov, Sergey V.; Catherine McCammon; Ilya Kupenko; Leyla Ismailova; Leonid Dubrovinsky

    2016-01-01

    Iron oxides are fundamentally important compounds for basic and applied sciences as well as in numerous industrial applications. In this work we report the synthesis and investigation of a new binary iron oxide with the hitherto unknown stoichiometry of Fe7O9. This new oxide was synthesized at high-pressure high-temperature (HP-HT) conditions, and its black single crystals were successfully recovered at ambient conditions. By means of single crystal X-ray diffraction we determined that Fe7O9 ...

  5. In-Situ Incubation of Iron-Sulfide Mineral in Seawater Reveals Colonization by Iron-Oxidizing Gammaproteobacteria and Zetaproteobacteria.

    Science.gov (United States)

    Barco, R. A.; Ramírez, G. A.; Sylvan, J. B.; Edwards, K. J.

    2015-12-01

    Sulfide mineral precipitation occurs at mid-ocean ridge (MOR) spreading centers, both in the form of plume particles and massive sulfide structures. A common constituent of MOR sulfide mineral is pyrrhotite (Fe1-xS). This mineral was chosen as a substrate for in-situ incubation studies in the shallow waters of Catalina Islands, CA to investigate the colonization of iron-oxidizing bacteria. Gammaproteobacteria and Alphaproteobacteria largely dominated the bacterial community on pyrrhotite samples incubated in the water column. Pyrrhotite samples incubated at the sediment/water column interface showed more even dominance by Gammaproteobacteria, Alphaproteobacteria, Deltaproteobacteria and Bacteroidetes. Cultivations that originated from these pyrrhotite samples resulted in the enrichment of Zetaproteobacteria with either twisted-stalks (Mariprofundus) or sheath structures. Additionally, a candidate novel Gammaproteobacterium was isolated and shown to grow autotrophically via the oxidation of iron.

  6. Degradation of organophosphorus pesticide parathion methyl on nanostructured titania-iron mixed oxides

    Science.gov (United States)

    Henych, Jiří; Štengl, Václav; Slušná, Michaela; Matys Grygar, Tomáš; Janoš, Pavel; Kuráň, Pavel; Štastný, Martin

    2015-07-01

    Titania-iron mixed oxides with various Ti:Fe ratio were prepared by homogeneous hydrolysis of aqueous solutions of titanium(IV) oxysulphate and iron(III) sulphate with urea as a precipitating agent. The synthesized samples were characterized by X-ray diffraction, Raman and infrared spectroscopy, scanning and transmission electron microscopy, XRF analysis, specific surface area (BET) and porosity determination (BJH). These oxides were used for degradation of organophosporus pesticide parathion methyl. The highest degradation efficiency approaching degraded on the surfaces of pure oxides. In general, the highest degradation rate exhibited samples consisted of the iron or titanium oxide containing a moderate amount of the admixture. However, distinct correlations between the degradation rate and the sorbent composition were not identified.

  7. Risk of Oxidative Damage to Bone from Increased Iron Stores During Space Flight

    Science.gov (United States)

    Zwart, S. R.; Smith, S. M.

    2014-01-01

    Iron stores are increased secondary to neocytolysis of red blood cells and a high dietary intake of iron during space flight. This raises concerns about the risk of excess iron causing oxidative damage in many tissues, including bone. Biomarkers of iron status, oxidative damage, and bone resorption during space flight were analyzed for 23 (16 M/7 F) International Space Station crewmembers as part of the Nutrition SMO project. Up to 5 in-flight blood samples and 24-h urine pools were collected over the course of the 4-6 month missions. Serum iron increased slightly during space flight and was decreased at landing (P diet (45 mg iron (ferric citrate)/kg diet) for 3 wk and then assigned to one of four groups: adequate iron (Fe) diet/no radiation, adequate Fe diet/ radiation, moderately high Fe diet (650 mg Fe (ferric citrate)/kg diet)/no radiation, and moderately high Fe diet/radiation. Animals remained on the assigned diet for 4 wk. Starting on day 14 of experimental diet treatment, animals were exposed to a fractionated dose (0.375 Gy) of Cs-137 every other day (3 Gy total dose). On day 29 (24 h after last radiation exposure), animals were euthanized. Oxidative stress markers in the liver, bone, eyes, and serum were assessed. There was evidence that the iron diet contributed to DNA damage as well as radiation exposure in the liver, eyes, and bone. Together, the results suggest that increased iron stores do constitute a risk factor for oxidative damage and bone resorption, during space flight and on Earth. Funded by the Human Health and Countermeasures Element of the NASA Human Research Program.

  8. Role of manganese in protection against oxidative stress under iron starvation in cyanobacterium Anabaena 7120.

    Science.gov (United States)

    Kaushik, Manish Singh; Srivastava, Meenakshi; Verma, Ekta; Mishra, Arun Kumar

    2015-06-01

    The cyanobacterium Anabaena sp. PCC 7120 was grown in presence and absence of iron to decipher the role of manganese in protection against the oxidative stress under iron starvation and growth, manganese uptake kinetics, antioxidative enzymes, lipid peroxidation, electrolyte leakage, thiol content, total peroxide, proline and NADH content was investigated. Manganese supported the growth of cyanobacterium Anabaena 7120 under iron deprived conditions where maximum uptake rate of manganese was observed with lower K(m) and higher V(max) values. Antioxidative enzymes were also found to be elevated in iron-starved conditions. Estimation of lipid peroxidation and electrolyte leakage depicted the role of manganese in stabilizing the integrity of the membrane which was considered as the prime target of oxygen free radicals in oxidative stress. The levels of total peroxide, thiol, proline and NADH content, which are the representative of oxidative stress response in Anabaena 7120, were also showed increasing trends in iron starvation. Hence, the results discerned, clearly suggested the role of manganese in protection against the oxidative stress in cyanobacterium Anabaena 7120 under iron starvation either due to its antioxidative properties or involvement as cofactor in a number of antioxidative enzymes.

  9. Assembly and Succession of Iron Oxide Microbial Mat Communities in Acidic Geothermal Springs

    Energy Technology Data Exchange (ETDEWEB)

    Beam, Jake; Bernstein, Hans C.; Jay, Z.; Kozubal, Mark; Jennings, Ryan; Tringe, Susannah G.; Inskeep, William P.

    2016-02-15

    Iron oxide microbial mats are ubiquitous geobiological features on Earth and occur in extant acidic hot springs of Yellowstone National Park (YNP), WY, USA, and form as a result of microbial processes. The relative contribution of different organisms to the development of these mat ecosystems is of specific interest. We hypothesized that chemolithoautotrophic organisms contribute to the early development and production of Fe(III)-oxide mats, which could support later-colonizing heterotrophic microorganisms. Sterile glass slides were incubated in the outflow channels of two acidic geothermal springs in YNP, and spatiotemporal changes in Fe(III)-oxide accretion and abundance of relevant community members were measured. Lithoautotrophic Hydrogenobaculum spp. were first colonizers and the most abundant taxa identified during early successional stages (7 – 40 days). Populations of M. yellowstonensis colonized after ~ 7 days, corresponding to visible Fe(III)-oxide accretion. Heterotrophic archaea colonized after 30 days, and emerge as the dominant functional guild in mature iron oxide mats (1 – 2 cm thick) that form after 70 – 120 days. First-order rate constants of iron oxide accretion ranged from 0.05 – 0.046 day-1, and reflected the absolute amount of iron accreted. Micro- and macroscale microterracettes were identified during iron oxide mat development, and suggest that the mass transfer of oxygen limits microbial growth. This was also demonstrated using microelectrode measurements of oxygen as a function of mat depth, which showed steep gradients in oxygen from the aqueous mat interface to ~ 1 mm. The formation and succession of amorphous Fe(III)-oxide mat communities follows a predictable pattern of distinct stages and growth. The successional stages and microbial signatures observed in these extant Fe(III)-oxide mat communities may be relevant to other past or present Fe(III)-oxide mineralizing systems.

  10. Iron oxidation kinetics study by using infrared spectral emissivity measurements below 570deg. C

    Energy Technology Data Exchange (ETDEWEB)

    Campo, Leire del [Departamento de Fisica de la Materia Condensada, Facultad de Ciencia y Tecnologi' a, Universidad del Pai' s Vasco, Barrio Sarriena s/n, 48940 Leioa, Bizkaia (Spain); Perez-Saez, Raul B. [Departamento de Fisica de la Materia Condensada, Facultad de Ciencia y Tecnologi' a, Universidad del Pai' s Vasco, Barrio Sarriena s/n, 48940 Leioa, Bizkaia (Spain); Instituto de Sintesis y Estudio de Materiales, Universidad del Pais Vasco, Apdo. 644, 48080 Bilbao (Spain)], E-mail: raul.perez@ehu.es; Tello, Manuel J. [Departamento de Fisica de la Materia Condensada, Facultad de Ciencia y Tecnologi' a, Universidad del Pai' s Vasco, Barrio Sarriena s/n, 48940 Leioa, Bizkaia (Spain); Instituto de Sintesis y Estudio de Materiales, Universidad del Pais Vasco, Apdo. 644, 48080 Bilbao (Spain)

    2008-01-15

    The oxidation kinetics of iron below 570deg. C is investigated through the dependence of the spectral emissivity on the surface oxidation state. Using the theory of radiative effects of thin films, the oxide scale thickness is obtained as a function of time. A parabolic growth has been observed in all the cases, and applying Wagner's theory, the oxidation parabolic rate constants have been calculated at four temperatures. The temperature dependence of these results has additionally been used to obtain the activation energy of the oxidation process in iron. The parabolic rate constants and activation energy values are in good agreement with the theoretical predictions, and this suggests that the lattice diffusion mechanisms for the high temperature magnetite growth also occur until 400deg. C. The experimental results are also useful to test the applicability of emissivity measurements for in situ oxidation kinetics studies in the spectral range where the scales are optically thin.

  11. Ceruloplasmin Oxidation, a Feature of Parkinson's Disease CSF, Inhibits Ferroxidase Activity and Promotes Cellular Iron Retention

    KAUST Repository

    Olivieri, S.

    2011-12-14

    Parkinson\\'s disease is a neurodegenerative disorder characterized by oxidative stress and CNS iron deposition. Ceruloplasmin is an extracellular ferroxidase that regulates cellular iron loading and export, and hence protects tissues from oxidative damage. Using two-dimensional electrophoresis, we investigated ceruloplasmin patterns in the CSF of human Parkinson\\'s disease patients. Parkinson\\'s disease ceruloplasmin profiles proved more acidic than those found in healthy controls and in other human neurological diseases (peripheral neuropathies, amyotrophic lateral sclerosis, and Alzheimer\\'s disease); degrees of acidity correlated with patients\\' pathological grading. Applying an unsupervised pattern recognition procedure to the two-dimensional electrophoresis images, we identified representative pathological clusters. In vitro oxidation of CSF in two-dimensional electrophoresis generated a ceruloplasmin shift resembling that observed in Parkinson\\'s disease and co-occurred with an increase in protein carbonylation. Likewise, increased protein carbonylation was observed in Parkinson\\'s disease CSF, and the same modification was directly identified in these samples on ceruloplasmin. These results indicate that ceruloplasmin oxidation contributes to pattern modification in Parkinson\\'s disease. From the functional point of view, ceruloplasmin oxidation caused a decrease in ferroxidase activity, which in turn promotes intracellular iron retention in neuronal cell lines as well as in primary neurons, which are more sensitive to iron accumulation. Accordingly, the presence of oxidized ceruloplasmin in Parkinson\\'s disease CSF might be used as a marker for oxidative damage and might provide new insights into the underlying pathological mechanisms.

  12. Suppressing iron oxide nanoparticle toxicity by vascular targeted antioxidant polymer nanoparticles.

    Science.gov (United States)

    Cochran, David B; Wattamwar, Paritosh P; Wydra, Robert; Hilt, J Zach; Anderson, Kimberly W; Eitel, Richard E; Dziubla, Thomas D

    2013-12-01

    The biomedical use of superparamagnetic iron oxide nanoparticles has been of continued interest in the literature and clinic. Their ability to be used as contrast agents for imaging and/or responsive agents for remote actuation makes them exciting materials for a wide range of clinical applications. Recently, however, concern has arisen regarding the potential health effects of these particles. Iron oxide toxicity has been demonstrated in in vivo and in vitro models, with oxidative stress being implicated as playing a key role in this pathology. One of the key cell types implicated in this injury is the vascular endothelial cells. Here, we report on the development of a targeted polymeric antioxidant, poly(trolox ester), nanoparticle that can suppress oxidative damage. As the polymer undergoes enzymatic hydrolysis, active trolox is locally released, providing a long term protection against pro-oxidant agents. In this work, poly(trolox) nanoparticles are targeted to platelet endothelial cell adhesion molecules (PECAM-1), which are able to bind to and internalize in endothelial cells and provide localized protection against the cytotoxicity caused by iron oxide nanoparticles. These results indicate the potential of using poly(trolox ester) as a means of mitigating iron oxide toxicity, potentially expanding the clinical use and relevance of these exciting systems.

  13. Doxorubicin loaded PVA coated iron oxide nanoparticles for targeted drug delivery

    Energy Technology Data Exchange (ETDEWEB)

    Kayal, S. [School of Materials Science and Engineering, Nanyang Technological University, Singapore 639798 (Singapore); Ramanujan, R.V., E-mail: ramanujan@ntu.edu.sg [School of Materials Science and Engineering, Nanyang Technological University, Singapore 639798 (Singapore)

    2010-04-06

    Magnetic drug targeting is a drug delivery system that can be used in locoregional cancer treatment. Coated magnetic particles, called carriers, are very useful for delivering chemotherapeutic drugs. Magnetic carriers were synthesized by coprecipitation of iron oxide followed by coating with polyvinyl alcohol (PVA). Characterization was carried out using X-ray diffraction, TEM, TGA, FTIR and VSM techniques. The magnetic core of the carriers was magnetite (Fe{sub 3}O{sub 4}), with average size of 10 nm. The room temperature VSM measurements showed that magnetic particles were superparamagnetic. The amount of PVA bound to the iron oxide nanoparticles were estimated by thermogravimetric analysis (TGA) and the attachment of PVA to the iron oxide nanoparticles was confirmed by FTIR analysis. Doxorubicin (DOX) drug loading and release profiles of PVA coated iron oxide nanoparticles showed that up to 45% of adsorbed drug was released in 80 h, the drug release followed the Fickian diffusion-controlled process. The binding of DOX to the PVA was confirmed by FTIR analysis. The present findings show that DOX loaded PVA coated iron oxide nanoparticles are promising for magnetically targeted drug delivery.

  14. Preparation and characterization of thermosensitive PNIPAA-coated iron oxide nanoparticles

    Science.gov (United States)

    Zhang, Shengmao; Zhang, Linna; He, Benfang; Wu, Zhishen

    2008-08-01

    A new and facile approach was established to fabricate thermoresponsive poly(N-isopropylacrylamide) (PNIPAA) coated iron oxide nanoparticles in a non-aqueous medium. The morphology and structure of the nanoparticle-doped composite were analyzed by means of transmission electron microscopy (TEM), x-ray powder diffraction (XRD), and Fourier transformation infrared spectrometry (FTIR). The thermosensitivity of the composite was also investigated. Results indicated that the oil-soluble iron oxide nanoparticles encapsulated with PNIPAA, composed of an inorganic iron oxide core and biocompatible PNIPAA shell, were dispersed well in water and had a sphere-like shape. The PNIPAA-coated iron oxide nanoparticles with such a kind of core-shell structure showed excellent thermosensitivity. Namely, the aqueous suspension of PNIPAA-coated iron oxide nanoparticles dramatically changed from transparent to opaque as the temperature increased from room temperature to 38 °C, showing potential as optical transmittance switch materials and their significance in the fields of protein adsorption and purification controlled release, and drug delivery.

  15. Biomedical microdevices synthesis of iron oxide nanoparticles using a microfluidic system.

    Science.gov (United States)

    Lee, Wen-Bin; Weng, Chen-Hsun; Cheng, Fong-Yu; Yeh, Chen-Sheng; Lei, Huan-Yao; Lee, Gwo-Bin

    2009-02-01

    The preparation of nanoparticles is essential in the application of many nanotechnologies and various preparation methods have been explored in the previous decades. Among them, iron oxide nanoparticles have been widely investigated in applications ranging from bio-imaging to bio-sensing due to their unique magnetic properties. Recently, microfluidic systems have been utilized for synthesis of nanoparticles, which have the advantages of automation, well-controlled reactions, and a high particle uniformity. In this study, a new microfluidic system capable of mixing, transporting and reacting was developed for the synthesis of iron oxide nanoparticles. It allowed for a rapid and efficient approach to accelerate and automate the synthesis of the iron oxide nanoparticles as compared with traditional methods. The microfluidic system uses micro-electro-mechanical-system technologies to integrate a new double-loop micromixer, two micropumps, and a microvalve on a single chip. When compared with large-scale synthesis systems with commonly-observed particle aggregation issues, successful synthesis of dispersed and uniform iron oxide nanoparticles has been observed within a shorter period of time (15 min). It was found that the size distribution of these iron oxide nanoparticles is superior to that of the large-scale systems without requiring any extra additives or heating. The size distribution had a variation of 16%. This is much lower than a comparable large-scale system (34%). The development of this microfluidic system is promising for the synthesis of nanoparticles for many future biomedical applications.

  16. Magnetic and gravity gradiometry framework for Mesoproterozoic iron oxide-apatite and iron oxide-copper-gold deposits, southeast Missouri, USA

    Science.gov (United States)

    McCafferty, Anne E.; Phillips, Jeffrey; Driscoll, Rhonda L.

    2016-01-01

    High-resolution airborne magnetic and gravity gradiometry data provide the geophysical framework for evaluating the exploration potential of hidden iron oxide deposits in Mesoproterozoic basement rocks of southeast Missouri. The data are used to calculate mineral prospectivity for iron oxide-apatite (IOA) ± rare earth element (REE) and iron oxide-copper-gold (IOCG) deposits. Results delineate the geophysical footprints of all known iron oxide deposits and reveal several previously unrecognized prospective areas. The airborne data are also inverted to three-dimensional density and magnetic susceptibility models over four concealed deposits at Pea Ridge (IOA ± REE), Boss (IOCG), Kratz Spring (IOA), and Bourbon (IOCG). The Pea Ridge susceptibility model shows a magnetic source that is vertically extensive and traceable to a depth of greater than 2 km. A smaller density source, located within the shallow Precambrian basement, is partly coincident with the magnetic source at Pea Ridge. In contrast, the Boss models show a large (625-m-wide), vertically extensive, and coincident dense and magnetic stock with shallower adjacent lobes that extend more than 2,600 m across the shallow Precambrian paleosurface. The Kratz Spring deposit appears to be a smaller volume of iron oxides and is characterized by lower density and less magnetic rock compared to the other iron deposits. A prospective area identified south of the Kratz Spring deposit shows the largest volume of coincident dense and nonmagnetic rock in the subsurface, and is interpreted as prospective for a hematite-dominant lithology that extends from the top of the Precambrian to depths exceeding 2 km. The Bourbon deposit displays a large bowl-shaped volume of coincident high density and high-magnetic susceptibility rock, and a geometry that suggests the iron mineralization is vertically restricted to the upper parts of the Precambrian basement. In order to underpin the evaluation of the prospectivity and three

  17. Deposition of Biogenic Iron Minerals in a Methane Oxidizing Microbial Mat

    Directory of Open Access Journals (Sweden)

    Christoph Wrede

    2013-01-01

    Full Text Available The syntrophic community between anaerobic methanotrophic archaea and sulfate reducing bacteria forms thick, black layers within multi-layered microbial mats in chimney-like carbonate concretions of methane seeps located in the Black Sea Crimean shelf. The microbial consortium conducts anaerobic oxidation of methane, which leads to the formation of mainly two biomineral by-products, calcium carbonates and iron sulfides, building up these chimneys. Iron sulfides are generated by the microbial reduction of oxidized sulfur compounds in the microbial mats. Here we show that sulfate reducing bacteria deposit biogenic iron sulfides extra- and intracellularly, the latter in magnetosome-like chains. These chains appear to be stable after cell lysis and tend to attach to cell debris within the microbial mat. The particles may be important nuclei for larger iron sulfide mineral aggregates.

  18. Deposition of biogenic iron minerals in a methane oxidizing microbial mat.

    Science.gov (United States)

    Wrede, Christoph; Kokoschka, Sebastian; Dreier, Anne; Heller, Christina; Reitner, Joachim; Hoppert, Michael

    2013-01-01

    The syntrophic community between anaerobic methanotrophic archaea and sulfate reducing bacteria forms thick, black layers within multi-layered microbial mats in chimney-like carbonate concretions of methane seeps located in the Black Sea Crimean shelf. The microbial consortium conducts anaerobic oxidation of methane, which leads to the formation of mainly two biomineral by-products, calcium carbonates and iron sulfides, building up these chimneys. Iron sulfides are generated by the microbial reduction of oxidized sulfur compounds in the microbial mats. Here we show that sulfate reducing bacteria deposit biogenic iron sulfides extra- and intracellularly, the latter in magnetosome-like chains. These chains appear to be stable after cell lysis and tend to attach to cell debris within the microbial mat. The particles may be important nuclei for larger iron sulfide mineral aggregates.

  19. Microwave-Assisted Combustion Synthesis of Nano Iron Oxide/Iron-Coated Activated Carbon, Anthracite, Cellulose Fiber, and Silica, with Arsenic Adsorption Studies

    Directory of Open Access Journals (Sweden)

    Mallikarjuna N. Nadagouda

    2011-01-01

    Full Text Available Combustion synthesis of iron oxide/iron coated carbons such as activated carbon, anthracite, cellulose fiber, and silica is described. The reactions were carried out in alumina crucibles using a Panasonic kitchen microwave with inverter technology, and the reaction process was completed within a few minutes. The method used no additional fuel and nitrate, which is present in the precursor itself, to drive the reaction. The obtained samples were then characterized with X-ray mapping, scanning electron microscopy (SEM, energy dispersive X-ray analysis (EDS, selected area diffraction pattern (SAED, transmission electron microscopy (TEM, X-ray diffraction (XRD, and inductively coupled plasma (ICP spectroscopy. The size of the iron oxide/iron nanoparticle-coated activated carbon, anthracite, cellulose fiber, and silica samples were found to be in the nano range (50–400 nm. The iron oxide/iron nanoparticles mostly crystallized into cubic symmetry which was confirmed by SAED. The XRD pattern indicated that iron oxide/iron nano particles existed in four major phases. That is, γ-Fe2O3, α-Fe2O3, Fe3O4, and Fe. These iron-coated activated carbon, anthracite, cellulose fiber, and silica samples were tested for arsenic adsorption through batch experiments, revealing that few samples had significant arsenic adsorption.

  20. Nitric oxide accumulation is required to protect against iron-mediated oxidative stress in frataxin-deficient Arabidopsis plants.

    Science.gov (United States)

    Martin, Mariana; Colman, María José Rodríguez; Gómez-Casati, Diego F; Lamattina, Lorenzo; Zabaleta, Eduardo Julián

    2009-02-04

    Frataxin is a mitochondrial protein that is conserved throughout evolution. In yeast and mammals, frataxin is essential for cellular iron (Fe) homeostasis and survival during oxidative stress. In plants, frataxin deficiency causes increased reactive oxygen species (ROS) production and high sensitivity to oxidative stress. In this work we show that a knock-down T-DNA frataxin-deficient mutant of Arabidopsis thaliana (atfh-1) contains increased total and organellar Fe levels. Frataxin deficiency leads also to nitric oxide (NO) accumulation in both, atfh-1 roots and frataxin null mutant yeast. Abnormally high NO production might be part of the defence mechanism against Fe-mediated oxidative stress.

  1. Iron homeostasis and oxidative stress in idiopathic pulmonary alveolar proteinosis: a case-control study

    Directory of Open Access Journals (Sweden)

    Roggli Victor L

    2008-01-01

    Full Text Available Abstract Background Lung injury caused by both inhaled dusts and infectious agents depends on increased availability of iron and metal-catalyzed oxidative stress. Because inhaled particles, such as silica, and certain infections can cause secondary pulmonary alveolar proteinosis (PAP, we tested the hypothesis that idiopathic PAP is associated with an altered iron homeostasis in the human lung. Methods Healthy volunteers (n = 20 and patients with idiopathic PAP (n = 20 underwent bronchoalveolar lavage and measurements were made of total protein, iron, tranferrin, transferrin receptor, lactoferrin, and ferritin. Histochemical staining for iron and ferritin was done in the cell pellets from control subjects and PAP patients, and in lung specimens of patients without cardiopulmonary disease and with PAP. Lavage concentrations of urate, glutathione, and ascorbate were also measured as indices of oxidative stress. Results Lavage concentrations of iron, transferrin, transferrin receptor, lactoferrin, and ferritin were significantly elevated in PAP patients relative to healthy volunteers. The cells of PAP patients had accumulated significant iron and ferritin, as well as considerable amounts of extracellular ferritin. Immunohistochemistry for ferritin in lung tissue revealed comparable amounts of this metal-storage protein in the lower respiratory tract of PAP patients both intracellularly and extracellularly. Lavage concentrations of ascorbate, glutathione, and urate were significantly lower in the lavage fluid of the PAP patients. Conclusion Iron homeostasis is altered in the lungs of patients with idiopathic PAP, as large amounts of catalytically-active iron and low molecular weight anti-oxidant depletion are present. These findings suggest a metal-catalyzed oxidative stress in the maintenance of this disease.

  2. Inositol hexa phosphoric acid (phytic acid), a nutraceuticals, attenuates iron-induced oxidative stress and alleviates liver injury in iron overloaded mice.

    Science.gov (United States)

    Bhowmik, Anwesha; Ojha, Durbadal; Goswami, Debayan; Das, Rashmi; Chandra, Nidhi S; Chatterjee, Tapan K; Chakravarty, Amit; Chakravarty, Sudipa; Chattopadhyay, Debprasad

    2017-03-01

    Inositol hexa phosphoric acid (IP6) or Phytic acid, a natural antioxidant of some leguminous plants, known to act as a protective agent for seed storage in plants by suppressing iron catalyzed oxidative process. Following the same mechanism, we have tested the effect of IP6 on iron overloaded in vitro oxidative stress, and studied it's in vivo hepatoprotective ability in iron-dextran (injection)-induced iron overloaded liver injury in mice (intraperitoneal). Our results showed that IP6 had in vitro iron chelation (IC50 38.4μg/ml) activity, with the inhibition of iron-induced lipid peroxidation (IC50 552μg/ml), and deoxyribose sugar degrading hydroxyl radicals (IC50 448.6μg/ml). Oral administration of IP6 (0-200mg/kg) revealed significant decrease in biochemical markers such as serum iron, total iron binding, serum ferritin and serum enzymes. Histopathology of liver stained with hematoxylin-eosin and Prussian blue showed reduced hepatocellular necrosis, ballooning and inflammation, indicating the restoration of normal cellular integrity. Interestingly, the IP6 was found to down-regulate the mRNA expression of tumor necrosis factor (TNF)-α, Interleukin (IL)-1β, and IL-6 in iron overloaded liver tissues. Thus, we provide an insight that IP6, a natural food component, can serve as an iron chelator against iron overload diseases like Thalassemia, and also as a dietary hepatoprotective supplement.

  3. Iron oxide nanoparticles for plant nutrition? A preliminary Mössbauer study

    Science.gov (United States)

    Homonnay, Z.; Tolnai, Gy.; Fodor, F.; Solti, Á.; Kovács, K.; Kuzmann, E.; Ábrahám, A.; Szabó, E. Gy.; Németh, P.; Szabó, L.; Klencsár, Z.

    2016-12-01

    One of the most important micronutrients for plants is iron. We have prepared iron(III) oxyhydroxide and magnetite nanoparticles with the aim to use them as possible nutrition source for plants. The iron(III)-oxide/oxyhydroxide nanoparticles prepared under our experimental conditions as colloidal suspensions proved to be 6-line ferrihydrite nanoparticles as verified by XRD, TEM/SAED and Mössbauer spectroscopy measurements. 57Fe Mössbauer spectra of magnetite nanoparticles prepared under different preparation conditions could be analyzed on the basis of a common model based on the superposition of four sextet components displaying Gaussian-shaped hyperfine magnetic field distributions.

  4. Ocean productivity before about 1.9 Gyr ago limited by phosphorus adsorption onto iron oxides.

    Science.gov (United States)

    Bjerrum, Christian J; Canfield, Donald E

    2002-05-09

    After the evolution of oxygen-producing cyanobacteria at some time before 2.7 billion years ago, oxygen production on Earth is thought to have depended on the availability of nutrients in the oceans, such as phosphorus (in the form of orthophosphate). In the modern oceans, a significant removal pathway for phosphorus occurs by way of its adsorption onto iron oxide deposits. Such deposits were thought to be more abundant in the past when, under low sulphate conditions, the formation of large amounts of iron oxides resulted in the deposition of banded iron formations. Under these circumstances, phosphorus removal by iron oxide adsorption could have been enhanced. Here we analyse the phosphorus and iron content of banded iron formations to show that ocean orthophosphate concentrations from 3.2 to 1.9 billion years ago (during the Archaean and early Proterozoic eras) were probably only approximately 10-25% of present-day concentrations. We suggest therefore that low phosphorus availability should have significantly reduced rates of photosynthesis and carbon burial, thereby reducing the long-term oxygen production on the early Earth--as previously speculated--and contributing to the low concentrations of atmospheric oxygen during the late Archaean and early Proterozoic.

  5. Extending the models for iron and sulfur oxidation in the extreme Acidophile Acidithiobacillus ferrooxidans

    Directory of Open Access Journals (Sweden)

    Holmes David S

    2009-08-01

    Full Text Available Abstract Background Acidithiobacillus ferrooxidans gains energy from the oxidation of ferrous iron and various reduced inorganic sulfur compounds at very acidic pH. Although an initial model for the electron pathways involved in iron oxidation has been developed, much less is known about the sulfur oxidation in this microorganism. In addition, what has been reported for both iron and sulfur oxidation has been derived from different A. ferrooxidans strains, some of which have not been phylogenetically characterized and some have been shown to be mixed cultures. It is necessary to provide models of iron and sulfur oxidation pathways within one strain of A. ferrooxidans in order to comprehend the full metabolic potential of the pangenome of the genus. Results Bioinformatic-based metabolic reconstruction supported by microarray transcript profiling and quantitative RT-PCR analysis predicts the involvement of a number of novel genes involved in iron and sulfur oxidation in A. ferrooxidans ATCC23270. These include for iron oxidation: cup (copper oxidase-like, ctaABT (heme biogenesis and insertion, nuoI and nuoK (NADH complex subunits, sdrA1 (a NADH complex accessory protein and atpB and atpE (ATP synthetase F0 subunits. The following new genes are predicted to be involved in reduced inorganic sulfur compounds oxidation: a gene cluster (rhd, tusA, dsrE, hdrC, hdrB, hdrA, orf2, hdrC, hdrB encoding three sulfurtransferases and a heterodisulfide reductase complex, sat potentially encoding an ATP sulfurylase and sdrA2 (an accessory NADH complex subunit. Two different regulatory components are predicted to be involved in the regulation of alternate electron transfer pathways: 1 a gene cluster (ctaRUS that contains a predicted iron responsive regulator of the Rrf2 family that is hypothesized to regulate cytochrome aa3 oxidase biogenesis and 2 a two component sensor-regulator of the RegB-RegA family that may respond to the redox state of the quinone pool

  6. Magnetic iron oxide nanoparticles as drug delivery system in breast cancer

    Energy Technology Data Exchange (ETDEWEB)

    Marcu, A., E-mail: marcu@ifin.nipne.ro [National Institute for Laser, Plasma and Radiation Physics, Atomistilor 409, P.O. Box MG 36, Bucharest-Magurele (Romania); Pop, S. [“Victor Babes” National Institute of Pathology, 99-101 Splaiul Independentei, 050096 Bucharest (Romania); Dumitrache, F. [National Institute for Laser, Plasma and Radiation Physics, Atomistilor 409, P.O. Box MG 36, Bucharest-Magurele (Romania); Mocanu, M.; Niculite, C.M.; Gherghiceanu, M. [“Victor Babes” National Institute of Pathology, 99-101 Splaiul Independentei, 050096 Bucharest (Romania); Lungu, C.P.; Fleaca, C. [National Institute for Laser, Plasma and Radiation Physics, Atomistilor 409, P.O. Box MG 36, Bucharest-Magurele (Romania); Ianchis, R. [National Institute for Research and Development in Chemistry and Petrochemistry, 202 Splaiul Independentei, 060021 Bucharest (Romania); Barbut, A.; Grigoriu, C.; Morjan, I. [National Institute for Laser, Plasma and Radiation Physics, Atomistilor 409, P.O. Box MG 36, Bucharest-Magurele (Romania)

    2013-09-15

    Present work was focused on producing improved iron oxide nanoparticles for targeted drug delivery in breast cancer. Nanometric-sized iron oxide particles were synthesized by laser pyrolysis and were morphologically/structurally characterized. These new nanoparticles were compared with some commercial, chemically prepared iron oxide ones. Cytotoxicity and the anti-proliferation effects of nanoparticles were tested in vitro on the breast adenocarcinoma cell line MCF-7. Nanoparticles were further coated with the antracyclinic antibiotic Violamycine B1 and tested for the anti-tumor effect on MCF-7 cells. The nanoparticles produced by us seem more effective in vitro than the commercial ones, with respect to cellular uptake and VB1 delivery. Violamycine B1 bound on nanoparticles is as efficient as the free form, but is better delivered into tumor cells.

  7. Magnetic iron oxide nanoparticles as drug delivery system in breast cancer

    Science.gov (United States)

    Marcu, A.; Pop, S.; Dumitrache, F.; Mocanu, M.; Niculite, C. M.; Gherghiceanu, M.; Lungu, C. P.; Fleaca, C.; Ianchis, R.; Barbut, A.; Grigoriu, C.; Morjan, I.

    2013-09-01

    Present work was focused on producing improved iron oxide nanoparticles for targeted drug delivery in breast cancer. Nanometric-sized iron oxide particles were synthesized by laser pyrolysis and were morphologically/structurally characterized. These new nanoparticles were compared with some commercial, chemically prepared iron oxide ones. Cytotoxicity and the anti-proliferation effects of nanoparticles were tested in vitro on the breast adenocarcinoma cell line MCF-7. Nanoparticles were further coated with the antracyclinic antibiotic Violamycine B1 and tested for the anti-tumor effect on MCF-7 cells. The nanoparticles produced by us seem more effective in vitro than the commercial ones, with respect to cellular uptake and VB1 delivery. Violamycine B1 bound on nanoparticles is as efficient as the free form, but is better delivered into tumor cells.

  8. Functional Iron Oxide-Silver Hetero-Nanocomposites: Controlled Synthesis and Antibacterial Activity

    Science.gov (United States)

    Trang, Vu Thi; Tam, Le Thi; Van Quy, Nguyen; Huy, Tran Quang; Thuy, Nguyen Thanh; Tri, Doan Quang; Cuong, Nguyen Duy; Tuan, Pham Anh; Van Tuan, Hoang; Le, Anh-Tuan; Phan, Vu Ngoc

    2017-02-01

    Iron oxide-silver nanocomposites are of great interest for their antibacterial and antifungal activities. We report a two-step synthesis of functional magnetic hetero-nanocomposites of iron oxide nanoparticles and silver nanoparticles (Fe3O4-Ag). Iron oxide nanoparticles were prepared first by a co-precipitation method followed by the deposition of silver nanoparticles via a hydrothermal route. The prepared Fe3O4-Ag hetero-nanocomposites were characterized by x-ray diffraction, transmission electron microscopy, high resolution transmission electron microscopy and vibrating sample magnetometry. Their antibacterial activities were investigated by using paper-disc diffusion and direct-drop diffusion methods. The results indicate that the Fe3O4-Ag hetero-nanocomposites exhibit excellent antibacterial activities against two Gram-negative bacterial strains (Salmonella enteritidis and Klebsiella pneumoniae).

  9. Ex situ integration of iron oxide nanoparticles onto the exfoliated expanded graphite flakes in water suspension

    Directory of Open Access Journals (Sweden)

    Jović Nataša

    2014-01-01

    Full Text Available Hybrid structures composed of exfoliated expanded graphite (EG and iron oxide nanocrystals have been produced by an ex situ process. The iron oxide nanoparticles coated with meso-2,3-dimercaptosuccinic acid (DMSA, or poly(acrylic acid (PAA were integrated onto the exfoliated EG flakes by mixing their aqueous suspensions at room temperature under support of 1-ethyl-3-(3-dimethylaminopropylcarbodiimide (EDC and N-hydroxysuccin-nimide (NHS. EG flakes have been used both, naked and functionalized with branched polyethylenimine (PEI. Complete integration of two constituents has been achieved and mainteined stable for more than 12 months. No preferential spatial distribution of anchoring sites for attachement of iron oxide nanoparticles has been observed, regardless EG flakes have been used naked or functionalized with PEI molecules. The structural and physico-chemical characteristics of the exfoliated expanded graphite and its hybrids nanostructures has been investigated by SEM, TEM, FTIR and Raman techniques. [Projekat Ministarstva nauke Republike Srbije, br. 45015

  10. Aging of iron (hydr)oxides by heat treatment and effects on heavy metal binding

    DEFF Research Database (Denmark)

    Sørensen, Mette Abildgaard; Starckpoole, M. M.; Frenkel, A. I.

    2000-01-01

    oxides were transformed to hematite, which had a greater thermodynamic stability but less surface area than the initial products. Heat treatment also caused some volatilization of heavy metals (most notably, Hg). Leaching with water at pH 9 (L/S 10, 24 h) and weak acid extraction showed that heat......Amorphous iron (hydr)oxides are used to remove heavy metals from wastewater and in the treatment of air pollution control residues generated in waste incineration. In this study, iron oxides containing heavy metals (e.g., Pb, Hg, Cr, and Cd) were treated at 50, 600, and 900 °C to simulate...... their transformations caused by heat treatment prior to disposal or aging at a proper disposal site. The transformations were investigated by XRD, SEM, XANES, EXAFS, surface area measurements, pH static leaching tests, and extractions with oxalate and weak hydrochloric acid. It was found that at 600 and 900 °C the iron...

  11. Tunability of Size and Magnetic Moment of Iron Oxide Nanoparticles Synthesized by Forced Hydrolysis

    Directory of Open Access Journals (Sweden)

    Ben Sutens

    2016-07-01

    Full Text Available To utilize iron oxide nanoparticles in biomedical applications, a sufficient magnetic moment is crucial. Since this magnetic moment is directly proportional to the size of the superparamagnetic nanoparticles, synthesis methods of superparamagnetic iron oxide nanoparticles with tunable size are desirable. However, most existing protocols are plagued by several drawbacks. Presented here is a one-pot synthesis method resulting in monodisperse superparamagnetic iron oxide nanoparticles with a controllable size and magnetic moment using cost-effective reagents. The obtained nanoparticles were thoroughly characterized by transmission electron microscopy (TEM, X-ray diffraction (XRD and Fourier transform infrared (FT-IR measurements. Furthermore, the influence of the size on the magnetic moment of the nanoparticles is analyzed by superconducting quantum interference device (SQUID magnetometry. To emphasize the potential use in biomedical applications, magnetic heating experiments were performed.

  12. Decolorization of black liquor from bioethanol G2 production using iron oxide coating sands

    Science.gov (United States)

    Barlianti, Vera; Triwahyuni, Eka; Waluyo, Joko; Sari, Ajeng Arum

    2017-01-01

    Bioethanol G2 production using oil palm empty fruit bunch as raw material consists of four steps, namely pretreatment, hydrolysis, fermentation, and purification process. Pretreatment process generates black liquor that causes serious environmental pollution if it is released to the environment. The objective of this research is studying the ability of iron oxide coating sands to adsorb the color of black liquor. The iron oxide coating sands were synthesized from FeCl3.6H2O with quartz sands as support material. This research was conducted on batch mode using black liquor in various pH values. Result obtained that kind of iron oxide on quartz sands's surface was goethite. The result also indicated decreasing of color intensity of black liquor after adsorption process. This research supports local material utilization in environmental technology development to solve some environmental problems.

  13. Defective iron-oxide nanoparticles synthesised by high temperature plasma processing: a magnetic characterisation versus temperature

    Science.gov (United States)

    Balasubramanian, C.; Joseph, B.; Orpe, PB; Saini, NL; Mukherjee, S.; Dziedzic-Kocurek, K.; Stanek, J.; Di Gioacchino, D.; Marcelli, A.

    2016-11-01

    Magnetic properties and phase compositions of iron-oxide nanoparticles synthesised by a high temperature arc plasma route have been investigated by Mössbauer spectroscopy and high harmonic magnetic AC susceptibility measurements, and correlated with morphological and structural properties for different synthesis conditions. The Mössbauer spectra precisely determined the presence of different iron-oxide fractions in the investigated nanoparticles, while the high harmonic magnetic susceptibility measurements revealed the occurrence of metastable magnetic phases evolving in temperature and time. This study illustrates magnetic properties and dynamics of the magnetic configurations of iron-oxide nanoparticles grown by high temperature plasma, a process less explored so far but extremely useful for synthesising large numbers of nanoparticles for industrial applications.

  14. Synthesis and Characterization of Zinc Oxide and Iron Oxide Nanoparticles Using Sesbania grandiflora Leaf Extract as Reducing Agent

    Directory of Open Access Journals (Sweden)

    Sorna Prema Rajendran

    2017-01-01

    Full Text Available The objectives of this present study are to synthesize iron oxide and zinc oxide nanoparticles from different concentrations of Sesbania grandiflora leaf extract (5–20% using zinc nitrate and ferrous chloride as precursor materials and synthesized nanoparticles were characterized using UV-visible spectrometer, FTIR, X-ray diffraction, and SEM. The results showed that synthesized zinc oxide and iron oxide nanoparticles exhibited UV-visible absorption peaks at 235 nm and 220 nm, respectively, which indicated that both nanoparticles were photosensitive and the XRD study confirmed that both nanoparticles were crystalline in nature. In addition, FTIR was also used to analyze the various functional groups present in the synthesized nanoparticles. The SEM results reveal that zinc oxide nanoparticles were spherical in shape and having the particle size range of 15 to 35 nm whereas the iron oxide nanoparticles were nonspherical in shape with the size range of 25 to 60 nm. Application of synthesized nanoparticle on seafood effluent treatment was studied.

  15. Degradation of organophosphorus pesticide parathion methyl on nanostructured titania-iron mixed oxides

    Energy Technology Data Exchange (ETDEWEB)

    Henych, Jiří, E-mail: henych@iic.cas.cz [Department of Material Chemistry, Institute of Inorganic Chemistry AS CR v.v.i., 25068 Řež (Czech Republic); Štengl, Václav; Slušná, Michaela; Matys Grygar, Tomáš [Department of Material Chemistry, Institute of Inorganic Chemistry AS CR v.v.i., 25068 Řež (Czech Republic); Janoš, Pavel; Kuráň, Pavel; Štastný, Martin [Faculty of the Environment, J.E. Purkyně University, Králova Výšina 7, 400 96 Ústí nad Labem (Czech Republic)

    2015-07-30

    Highlights: • Ti–Fe mixed oxides were synthesized via low-temperature one-pot method. • Mixed oxides were used for degradation of parathion methyl. • Pure reference oxide samples showed no degradation ability. • Mixed oxides reached 70% degree of conversion of parathion methyl. - Abstract: Titania-iron mixed oxides with various Ti:Fe ratio were prepared by homogeneous hydrolysis of aqueous solutions of titanium(IV) oxysulphate and iron(III) sulphate with urea as a precipitating agent. The synthesized samples were characterized by X-ray diffraction, Raman and infrared spectroscopy, scanning and transmission electron microscopy, XRF analysis, specific surface area (BET) and porosity determination (BJH). These oxides were used for degradation of organophosporus pesticide parathion methyl. The highest degradation efficiency approaching <70% was found for the samples with Ti:Fe ratio 0.25:1 and 1:0.25. Contrary, parathion methyl was not degraded on the surfaces of pure oxides. In general, the highest degradation rate exhibited samples consisted of the iron or titanium oxide containing a moderate amount of the admixture. However, distinct correlations between the degradation rate and the sorbent composition were not identified.

  16. The life cycle of iron Fe(III) oxide: impact of fungi and bacteria

    Science.gov (United States)

    Bonneville, Steeve

    2014-05-01

    Iron oxides are ubiquitous reactive constituents of soils, sediments and aquifers. They exhibit vast surface areas which bind a large array of trace metals, nutrients and organic molecules hence controlling their mobility/reactivity in the subsurface. In this context, understanding the "life cycle" of iron oxide in soils is paramount to many biogeochemical processes. Soils environments are notorious for their extreme heterogeneity and variability of chemical, physical conditions and biological agents at play. Here, we present studies investigating the role of two biological agents driving iron oxide dynamics in soils, root-associated fungi (mycorrhiza) and bacteria. Mycorrhiza filaments (hypha) grow preferentially around, and on the surface of nutrient-rich minerals, making mineral-fungi contact zones, hot-spots of chemical alteration in soils. However, because of the microscopic nature of hyphae (only ~ 5 µm wide for up to 1 mm long) and their tendency to strongly adhere to mineral surface, in situ observations of this interfacial micro-environment are scarce. In a microcosm, ectomycorrhiza (Paxillus involutus) was grown symbiotically with a pine tree (Pinus sylvestris) in the presence of freshly-cleaved biotite under humid, yet undersaturated, conditions typical of soils. Using spatially-resolved ion milling technique (FIB), transmission electron microscopy and spectroscopy (TEM/STEM-EDS), synchrotron based X-ray microscopy (STXM), we were able to quantify the speciation of Fe at the biotite-hypha interface. The results shows that substantial oxidation of biotite structural-Fe(II) into Fe(III) subdomains occurs at the contact zone between mycorrhiza and biotite. Once formed, iron(III) oxides can reductively dissolve under suboxic conditions via several abiotic and microbial pathways. In particular, they serve as terminal electron acceptors for the oxidation of organic matter by iron reducing bacteria. We aimed here to understand the role of Fe(III) mineral

  17. AbstractApplication of Fenton-like process using iron nano oxides for pyrene removal from contaminated soils

    Directory of Open Access Journals (Sweden)

    S. Jorfi

    2014-05-01

    Conclusion: Fenton oxidation using iron nano oxides under defined optimum conditions and neutral pH, can be a suitable alternative to conventional Fenton for remediation of soils contaminated with pyrene.

  18. Thermal and magnetic properties of iron oxide colloids: influence of surfactants

    Science.gov (United States)

    Soares, Paula I. P.; Lochte, Frederik; Echeverria, Coro; Pereira, Laura C. J.; Coutinho, Joana T.; Ferreira, Isabel M. M.; Novo, Carlos M. M.; Borges, João P. M. R.

    2015-10-01

    Iron oxide nanoparticles (NPs) have been extensively studied in the last few decades for several biomedical applications such as magnetic resonance imaging, magnetic drug delivery and hyperthermia. Hyperthermia is a technique used for cancer treatment which consists in inducing a temperature of about 41-45 °C in cancerous cells through magnetic NPs and an external magnetic field. Chemical precipitation was used to produce iron oxide NPs 9 nm in size coated with oleic acid and trisodium citrate. The influence of both stabilizers on the heating ability and in vitro cytotoxicity of the produced iron oxide NPs was assessed. Physicochemical characterization of the samples confirmed that the used surfactants do not change the particles’ average size and that the presence of the surfactants has a strong effect on both the magnetic properties and the heating ability. The heating ability of Fe3O4 NPs shows a proportional increase with the increase of iron concentration, although when coated with trisodium citrate or oleic acid the heating ability decreases. Cytotoxicity assays demonstrated that both pristine and trisodium citrate Fe3O4 samples do not reduce cell viability. However, oleic acid Fe3O4 strongly reduces cell viability, more drastically in the SaOs-2 cell line. The produced iron oxide NPs are suitable for cancer hyperthermia treatment and the use of a surfactant brings great advantages concerning the dispersion of NPs, also allowing better control of the hyperthermia temperature.

  19. Fenton-like oxidation of 2,4,6-trinitrotoluene using different iron minerals.

    Science.gov (United States)

    Matta, Roger; Hanna, Khalil; Chiron, Serge

    2007-10-15

    Degradation of 2,4,6-trinitrotoluene (TNT) was investigated in presence of different oxidants (Fenton's reagent, sodium persulfate, peroxymonosulfate and potassium permanganate) and different iron minerals (ferrihydrite, hematite, goethite, lepidocrocite, magnetite and pyrite) either in aqueous solution or in soil slurry systems. Fenton's reagent was the only oxidant able to degrade TNT in solution (k(app)=0.0348 min(-1)). When using iron oxide as heterogeneous catalyst at pH 3, specific reaction rate constants per surface area were k(surf)=1.47.10(-3) L min(-1) m(-2) and k(surf)=0.177 L min(-1) m(-2) for magnetite and pyrite, respectively while ferric iron minerals were inefficient for TNT degradation. The major asset of iron mineral catalyzed Fenton-like treatment has been the complete oxidation of the pollutant avoiding the accumulation of possible toxic by-products. In soil slurry systems, 38% abatement of the initial TNT concentration (2 g/kg) was reached after 24 h treatment time at neutral pH. Rate limiting steps were the availability of soluble iron at neutral pH together with desorption of the TNT fraction sorbed on the clay mineral surfaces.

  20. Magnetic filtration of an iron oxide aerosol by means of magnetizable grates

    Institute of Scientific and Technical Information of China (English)

    A. Alvaro; J.M. Rodríguez; Paulo A. Augusto; A.M. Estévez

    2007-01-01

    The cleaning of gases with low concentrations of small ferromagnetic or paramagnetic particles is a difficult task for conventional filtration. A new alternative procedure, magnetic filtration, is used in this work.Iron oxide aerosol was generated by elutriation of iron oxide particles from a fluidized bed consisting of a mixture of Geldart-C iron oxide powder and large spherical Geldart-B sand particles. The aerosol was filtered by means of a magnetic filter which consisted of one, two or three iron grates staggered to each other. The experimental installation contained also an isokinetic sampling system and a Microtrac SRA 150 Particle Analyser.A theoretical expression for filtration efficiency was deduced from a previous model taking into account the different forces acting on the iron oxide particles. Experimental filtration efficiency matches quite well calculated theoretical efficiency. It was found that an increase in particle size,in the number of grates or in the applied magnetic field produced higher filtration efficiencies up to 100% in some cases. In all filtration experiments pressure drop through the magnetic filter was very small.

  1. Laser sintering of magnesia with nanoparticles of iron oxide and aluminum oxide

    Energy Technology Data Exchange (ETDEWEB)

    García, L.V.; Mendivil, M.I.; Roy, T.K. Das; Castillo, G.A. [Facultad de Ingenieria Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, Av. Pedro de Alba s/n, Cd. Universitaria, San Nicolas de los Garza, Nuevo Leon 66451 (Mexico); Shaji, S., E-mail: sshajis@yahoo.com [Facultad de Ingenieria Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, Av. Pedro de Alba s/n, Cd. Universitaria, San Nicolas de los Garza, Nuevo Leon 66451 (Mexico); CIIDIT, Universidad Autonoma de Nuevo Leon, Apodaca, Nuevo Leon (Mexico)

    2015-05-01

    Highlights: • Laser sintered MgO pellets with nanoparticles of Al{sub 2}O{sub 3} and Fe{sub 2}O{sub 3}. • Characterized these pellets by XRD, SEM and XPS. • Spinel formations were observed in both cases. • Changes in morphology and structure were analyzed. - Abstract: Nanoparticles of iron oxide (Fe{sub 2}O{sub 3}, 20–40 nm) and aluminum oxide (Al{sub 2}O{sub 3}, 50 nm) were mixed in different concentrations (3, 5 and 7 wt%) in a magnesium oxide (MgO) matrix. The mixture pellet was irradiated with 532 nm output from a Q-switched Nd:YAG laser using different laser fluence and translation speed for sintering. The refractory samples obtained were analyzed using X-ray diffraction technique, scanning electron microscopy and X-ray photoelectron spectroscopy. The results showed that the samples irradiated at translation speed of 110 μm/s and energy fluence of 1.7 J/cm{sup 2} with a concentration of 5 and 7 wt% of Fe{sub 2}O{sub 3} presented the MgFe{sub 2}O{sub 4} spinel-type phase. With the addition of Al{sub 2}O{sub 3} nanoparticles, at a translation speed of 110 μm/s and energy fluence of 1.7 J/cm{sup 2}, there were the formations of MgAl{sub 2}O{sub 4} spinel phase. The changes in morphologies and microstructure due to laser irradiation were analyzed.

  2. The acute toxicity of iron and copper: biomolecule oxidation and oxidative damage in rat liver.

    Science.gov (United States)

    Boveris, Alberto; Musacco-Sebio, Rosario; Ferrarotti, Nidia; Saporito-Magriñá, Christian; Torti, Horacio; Massot, Francisco; Repetto, Marisa G

    2012-11-01

    The transition metals iron (Fe) and copper (Cu) are needed at low levels for normal health and at higher levels they become toxic for humans and animals. The acute liver toxicity of Fe and Cu was studied in Sprague Dawley male rats (200 g) that received ip 0-60 mg/kg FeCl(2) or 0-30 mg/kg CuSO(4). Dose and time-responses were determined for spontaneous in situ liver chemiluminescence, phospholipid lipoperoxidation, protein oxidation and lipid soluble antioxidants. The doses linearly defined the tissue content of both metals. Liver chemiluminescence increased 4 times and 2 times after Fe and Cu overloads, with half maximal responses at contents (C(50%)) of 110 μgFe/g and 42 μgCu/g liver, and with half maximal time responses (t(1/2)) of 4h for both metals. Phospholipid peroxidation increased 4 and 1.8 times with C(50%) of 118 μg Fe/g and 45 μg Cu/g and with t(1/2) of 7h and 8h. Protein oxidation increased 1.6 times for Fe with C(50%) at 113 μg Fe/g and 1.2 times for Cu with 50 μg Cu/g and t(1/2) of 4h and 5h respectively. The accumulation of Fe and Cu in liver enhanced the rate of free radical reactions and produced oxidative damage. A similar free radical-mediated process, through the formation HO(•) and RO(•) by a Fenton-like homolytic scission of H(2)O(2) and ROOH, seems to operate as the chemical mechanism for the liver toxicity of both metals.

  3. Catechol versus bisphosphonate ligand exchange at the surface of iron oxide nanoparticles: towards multi-functionalization

    Science.gov (United States)

    Guénin, Erwann; Lalatonne, Yoann; Bolley, Julie; Milosevic, Irena; Platas-Iglesias, Carlos; Motte, Laurence

    2014-11-01

    We report an investigation of the ligand exchange at the surface of iron oxide nanoparticles in water. For this purpose we compared two strong chelating agents on the iron oxide surface containing catechol and bisphosphonate moieties. Interactions between the coating agents (catechol/bisphosphonate) and the nanoparticle's surface were studied by FTIR and DFT calculations. Ligand exchange experiments were performed using sonication and the exchange yield was characterized by FTIR and EDX. This methodology allowed introducing bisphosphonates with various functionalities (alkyne or biotin) permitting multi-functionalization.

  4. Structural effects on the magnetic hyperthermia properties of iron oxide nanoparticles

    Directory of Open Access Journals (Sweden)

    Eric C. Abenojar

    2016-10-01

    Full Text Available Magnetic iron oxide nanoparticles (IONPs are heavily explored as diagnostic and therapeutic agents due to their low cost, tunable properties, and biocompatibility. In particular, upon excitation with an alternating current (AC magnetic field, the NPs generate localized heat that can be exploited for therapeutic hyperthermia treatment of diseased cells or pathogenic microbes. In this review, we focus on how structural changes and inter-particle interactions affect the heating efficiency of iron oxide-based magnetic NPs. Moreover, we present an overview of the different approaches to evaluate the heating performance of IONPs and introduce a new theranostic modality based on magnetic imaging guided–hyperthermia.

  5. Structural effects on the magnetic hyperthermia properties of iron oxide nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Eric C. Abenojar; Sameera Wickramasinghe; Jesbaniris Bas-Concepcion; Anna Cristina S. Samia

    2016-01-01

    Magnetic iron oxide nanoparticles (IONPs) are heavily explored as diagnostic and therapeutic agents due to their low cost, tunable properties, and biocompatibility. In particular, upon excitation with an alternating current (AC) magnetic field, the NPs generate localized heat that can be exploited for therapeutic hyperthermia treatment of diseased cells or pathogenic microbes. In this review, we focus on how structural changes and inter-particle interactions affect the heating efficiency of iron oxide-based magnetic NPs. Moreover, we present an overview of the different approaches to evaluate the heating performance of IONPs and introduce a new theranostic modality based on magnetic imaging guided–hyperthermia.

  6. Iron oxides, divalent cations, silica, and the early earth phosphorus crisis

    DEFF Research Database (Denmark)

    Jones, C.; Nomosatryo, S.; Crowe, S.A.;

    2015-01-01

    and silica content of BIFs, we estimate that seawater in the Archean and early Proterozoic Eons likely contained 0.04–0.13 µM phosphorus, on average. These phosphorus limiting conditions could have favored primary production through photoferrotrophy at the expense of oxygenic photosynthesis until upwelling......As a nutrient required for growth, phosphorus regulates the activity of life in the oceans. Iron oxides sorb phosphorus from seawater, and through the Archean and early Proterozoic Eons, massive quantities of iron oxides precipitated from the oceans, producing a record of seawater chemistry...

  7. Textural and Mineralogical Characteristics of Microbial Fossils in Modern and Ancient Iron (oxyhydr)oxides

    Science.gov (United States)

    Potter, S. L.; Chan, M. A.; McPherson, B. J.

    2012-12-01

    The Jurassic Brushy Basin Member of the Morrison Formation contains extensive alkaline saline lacustrine deposits rich in diagenetic iron (oxyhydr)oxides that are well exposed on the Colorado Plateau of the southwestern USA. These early diagenetic iron (oxyhydr)oxide minerals are associated with preserved diatoms and other algal forms, identified via scanning electron microscope (SEM) in thin sections of representative samples. The minerals are also associated with macroscopic bioturbation features (e.g., charophytes, burrows and fossilized dinosaur bones). Algal forms with cellular elaboration are identified by HF dissolution of bioturbation structures and examination with SEM. Collectively, these features suggest biomediated textures are preserved in early diagenetic iron (oxyhydr)oxides, and can persist for tens of millions of years. Modern microbially precipitated iron (oxyhydr)oxides and ~100ka tufa terraces from a cold spring system along Ten Mile Graben in southern Utah, USA are compared with the Morrison examples to identify modern microbial fossils and document any differences and preservation changes during diagenesis over geologic time. Two distinct suites of elements (1. C, Fe, As and 2. C, S, Se) are associated with microbial fossils in both the modern and ancient tufas, as well as the ancient Morrison specimens. The occurrence of these distinctive trace element configurations in the iron (oxyhydr)oxide minerals suggest the suites could be potential markers for biosignatures. The presence of ferrihydrite in ~100ka fossil microbial mats suggests this thermodynamically unstable mineral may also be used as a biomarker. Diagnostic trace element suites and unusual mineral phases warrant further study for their potential as biomarkers. These terrestrial iron (oxyhydr)oxide examples will: 1) document specific biomediated textures and what their origins might be (related to different processes or species), 2) show how they might persist or respond to

  8. Phase change induced by polypyrrole in iron-oxide polypyrrole nanocomposite

    Indian Academy of Sciences (India)

    Komilla Suri; S Annapoorni; R P Tandon

    2001-12-01

    Nanocomposites of polypyrrole and iron oxide were prepared using simultaneous gelation and polymerization processes. Varied amounts of pyrrole monomer were added to a solution containing iron nitrate as precursor and 2-methoxy ethanol as solvent. The presence of oxide and polypyrrole was confirmed by using X-ray and FTIR techniques. Some of these nanocomposites exhibited magnetic behaviour. SEM studies of powders indicated presence of nanosized particles. Electrical conductivity studies of powders showed a slight variation in conductivity for lower concentration of pyrrole, with a sudden increase in conductivity at 15% of pyrrole concentration. A transition from a nonmagnetic to magnetic phase was also observed at the same concentration.

  9. Two-component magnetic structure of iron oxide nanoparticles mineralized in Listeria innocua protein cages

    Science.gov (United States)

    Usselman, Robert J.; Klem, Michael T.; Russek, Stephen E.; Young, Mark; Douglas, Trevor; Goldfarb, Ron B.

    2010-06-01

    Magnetometry was used to determine the magnetic properties of maghemite (γ-Fe2O3) nanoparticles formed within Listeria innocua protein cage. The electron magnetic resonance spectrum shows the presence of at least two magnetization components. The magnetization curves are explained by a sum of two Langevin functions in which each filled protein cage contains both a large magnetic iron oxide core plus an amorphous surface consisting of small noncoupled iron oxide spin clusters. This model qualitatively explains the observed decrease in the temperature dependent saturation moment and removes an unrealistic temperature dependent increase in the particle moment often observed in nanoparticle magnetization measurements.

  10. Formation of Fe(0-Nanoparticles via Reduction of Fe(II Compounds by Amino Acids and Their Subsequent Oxidation to Iron Oxides

    Directory of Open Access Journals (Sweden)

    K. Klačanová

    2013-01-01

    Full Text Available Iron nanoparticles were prepared by the reduction of central Fe(II ion in the coordination compounds with amino acid ligands. The anion of the amino acid used as a ligand acted as the reducing agent. Conditions for the reduction were very mild; the temperature did not exceed 52°C, and the optimum pH was between 9.5 and 9.7. The metal iron precipitated as a mirror on the flask or as a colloid in water. Identification of the product was carried out by measuring UV/VIS spectra of the iron nanoparticles in water. The iron nanoparticles were oxidized by oxygen yielding a mixture of iron oxides. Oxidation of Fe(0 to Fe(II took several seconds under air. The size and properties of iron oxide nanoparticles were studied by UV/VIS, TEM investigation, RTG diffractometry, Mössbauer spectroscopy, magnetometry, thermogravimetry, and GC/MS.

  11. Tucum-Do-Cerrado (Bactris setosa Mart.) Consumption Modulates Iron Homeostasis and Prevents Iron-Induced Oxidative Stress in the Rat Liver

    Science.gov (United States)

    Fustinoni-Reis, Adriana M.; Arruda, Sandra F.; Dourado, Lívia P. S.; da Cunha, Marcela S. B.; Siqueira, Egle M. A.

    2016-01-01

    This study investigated the effect of tucum-do-cerrado consumption in the oxidative status of iron-supplemented rats. Four groups of rats were treated: Control (AIN-93G), Tuc (AIN-93G added of tucum-do-cerrado), Fe (AIN-93G iron-enriched), or TucFe (AIN-93G with tucum-do-cerrado and iron-enriched) diet, for 30 days. Iron-enriched diet increased serum, liver, spleen, and intestine iron levels; transferrin saturation; liver lipid oxidation; mRNA levels of hepatic Hamp and Bmp6, and Nrf2 in the intestine. Tucum-do-cerrado consumption reduced spleen lipid and protein oxidation; mRNA levels of hepatic Hamp and Ftl, and increased serum antioxidant capacity and hepatic mRNA levels of Bmp6, Hmox1, Nqo1, and Nrf2. TucFe diet consumption abrogated the liver Hamp iron-induced up-regulation, prevented intestinal iron accumulation; hepatic lipid peroxidation; splenic protein damage, and the increase of catalase, glutathione reductase, and glutathione peroxidase activity in some tissues. These results suggest that tucum-do-cerrado protects tissues against oxidative damage, by reducing iron availability in liver and consequently inhibiting liver Hamp expression. PMID:26901220

  12. Tucum-Do-Cerrado (Bactris setosa Mart. Consumption Modulates Iron Homeostasis and Prevents Iron-Induced Oxidative Stress in the Rat Liver

    Directory of Open Access Journals (Sweden)

    Adriana M. Fustinoni-Reis

    2016-02-01

    Full Text Available This study investigated the effect of tucum-do-cerrado consumption in the oxidative status of iron-supplemented rats. Four groups of rats were treated: Control (AIN-93G, Tuc (AIN-93G added of tucum-do-cerrado, Fe (AIN-93G iron-enriched, or TucFe (AIN-93G with tucum-do-cerrado and iron-enriched diet, for 30 days. Iron-enriched diet increased serum, liver, spleen, and intestine iron levels; transferrin saturation; liver lipid oxidation; mRNA levels of hepatic Hamp and Bmp6, and Nrf2 in the intestine. Tucum-do-cerrado consumption reduced spleen lipid and protein oxidation; mRNA levels of hepatic Hamp and Ftl, and increased serum antioxidant capacity and hepatic mRNA levels of Bmp6, Hmox1, Nqo1, and Nrf2. TucFe diet consumption abrogated the liver Hamp iron-induced up-regulation, prevented intestinal iron accumulation; hepatic lipid peroxidation; splenic protein damage, and the increase of catalase, glutathione reductase, and glutathione peroxidase activity in some tissues. These results suggest that tucum-do-cerrado protects tissues against oxidative damage, by reducing iron availability in liver and consequently inhibiting liver Hamp expression.

  13. Microwave-assisted combustion synthesis of nano iron oxide/iron-coated activated carbon, anthracite, cellulose fiber, and silica, with arsenic adsorption studies

    Science.gov (United States)

    Combustion synthesis of iron oxide/iron coated carbons such as activated carbon, anthracite, cellulose fiber and silica is described. The reactions were carried out in alumina crucibles using a Panasonic kitchen microwave with inverter technology, and the reaction process was com...

  14. Tucum-Do-Cerrado (Bactris setosa Mart.) Consumption Modulates Iron Homeostasis and Prevents Iron-Induced Oxidative Stress in the Rat Liver.

    Science.gov (United States)

    Fustinoni-Reis, Adriana M; Arruda, Sandra F; Dourado, Lívia P S; da Cunha, Marcela S B; Siqueira, Egle M A

    2016-02-17

    This study investigated the effect of tucum-do-cerrado consumption in the oxidative status of iron-supplemented rats. Four groups of rats were treated: Control (AIN-93G), Tuc (AIN-93G added of tucum-do-cerrado), Fe (AIN-93G iron-enriched), or TucFe (AIN-93G with tucum-do-cerrado and iron-enriched) diet, for 30 days. Iron-enriched diet increased serum, liver, spleen, and intestine iron levels; transferrin saturation; liver lipid oxidation; mRNA levels of hepatic Hamp and Bmp6, and Nrf2 in the intestine. Tucum-do-cerrado consumption reduced spleen lipid and protein oxidation; mRNA levels of hepatic Hamp and Ftl, and increased serum antioxidant capacity and hepatic mRNA levels of Bmp6, Hmox1, Nqo1, and Nrf2. TucFe diet consumption abrogated the liver Hamp iron-induced up-regulation, prevented intestinal iron accumulation; hepatic lipid peroxidation; splenic protein damage, and the increase of catalase, glutathione reductase, and glutathione peroxidase activity in some tissues. These results suggest that tucum-do-cerrado protects tissues against oxidative damage, by reducing iron availability in liver and consequently inhibiting liver Hamp expression.

  15. High-valent iron in chemical and biological oxidations.

    Science.gov (United States)

    Groves, John T

    2006-04-01

    Various aspects of the reactivity of iron(IV) in chemical and biological systems are reviewed. Accumulated evidence shows that the ferryl species [Fe(IV)O](2+) can be formed under a variety of conditions including those related to the ferrous ion-hydrogen peroxide system known as Fenton's reagent. Early evidence that such a species could hydroxylate typical aliphatic C-H bonds included regioselectivities and stereospecificities for cyclohexanol hydroxylation that could not be accounted for by a freely diffusing hydroxyl radical. Iron(IV) porphyrin complexes are also found in the catalytic cycles of cytochrome P450 and chloroperoxidase. Model oxo-iron(IV) porphyrin complexes have shown reactivity similar to the proposed enzymatic intermediates. Mechanistic studies using mechanistically diagnostic substrates have implicated a radical rebound scenario for aliphatic hydroxylation by cytochrome P450. Likewise, several non-heme diiron hydroxylases, AlkB (Omega-hydroxylase), sMMO (soluble methane monooxygenase), XylM (xylene monooxygenase) and T4moH (toluene monooxygenase) all show clear indications of radical rearranged products indicating that the oxygen rebound pathway is a ubiquitous mechanism for hydrocarbon oxygenation by both heme and non-heme iron enzymes.

  16. IRON OXIDE NANOPARTICLES AS THERMAL SEEDS IN MAGNETIC HYPERTHERMIA THERAPY

    OpenAIRE

    2016-01-01

    we present the short review on Magnetic nanoparticle specifically for biomedical application. This study shows the overview on magnetic material properties and its biocompatibility. Here we are discussing some results of manufacturing iron nano particle in lab and its thermal propertie srelated to hyperthermia.  Keywords- Magnetic  nanoparticle (MNP).

  17. Arsenic bioremediation by biogenic iron oxides and sulfides

    NARCIS (Netherlands)

    Omoregie, E.; Couture, R.-M.; Van Cappellen, P.; Corkhill, C.L.; Charnock, J.M.; Polya, D.A.; Vaughan, D; Vanbroekhoven, K.; Lloyd, J.R.

    2013-01-01

    Microcosms containing sediment from an aquifer in Cambodia with naturally elevated levels of arsenic in the associated groundwater were used to evaluate the effectiveness of microbially mediated production of iron minerals for in situ As remediation. The microcosms were first incubated without amend

  18. Structural characterization, antibacterial and catalytic effect of iron oxide nanoparticles synthesised using the leaf extract of Cynometra ramiflora

    Science.gov (United States)

    Groiss, Silvia; Selvaraj, Raja; Varadavenkatesan, Thivaharan; Vinayagam, Ramesh

    2017-01-01

    In the present investigation, the leaf extract of Cynometra ramiflora was used to synthesize iron oxide nanoparticles. Within minutes of adding iron sulphate to the leaf extract, iron oxide nanoparticles were formed and thus, the method is very simple and fast. UV-VIS spectra showed the strong absorption band in the visible region. SEM images showed discrete spherical shaped particles and EDS spectra confirmed the iron and oxygen presence. The XRD results depicted the crystalline structure of iron oxide nanoparticles. FT-IR spectra portrayed the existence of functional groups of phytochemicals which are probably involved in the formation and stabilization of nanoparticles. The iron oxide nanoparticles exhibited effective inhibition against E. coli and S. epidermidis which may find its applications in the antibacterial drug development. Furthermore, the catalytic activity of the nanoparticles as Fenton-like catalyst was successfully investigated for the degradation of Rhodamine-B dye. This outcome could play a prominent role in the wastewater treatment.

  19. Fossilization of Iron-Oxidizing Bacteria at Hydrothermal Vents: a Useful Biosignature on Mars?

    Science.gov (United States)

    Leveille, R. J.; Lui, S.

    2009-05-01

    Iron oxidizing bacteria are ubiquitous in marine and terrestrial environments on Earth, where they often display distinctive cell morphologies and are commonly encrusted by minerals, especially bacteriogenic iron oxides and silica. Putative microfossils of iron oxidizing bacteria have been found in jaspers as old as 490Ma and microbial iron oxidation may be an ancient metabolic pathway. In order to investigate the usefulness of mineralized iron oxidizing bacteria as a biosignature, we have examined mineral samples collected from relict hydrothermal systems along Explorer Ridge, NE Pacific Ocean. In addition, microaerophilic, neutrophilic iron oxidizing bacteria, isolated from Pacific hydrothermal vents, were grown in a Fe-enriched seawater medium at constant pH (6.5) and oxygen concentration (5 percent) in a controlled bioreactor system. Both natural samples and experimental products were examined with a combination of variable pressure scanning electron microscopy (SEM), field emission gun SEM, and in some cases by preparing samples with a focused ion beam (FIB) milling system. Natural seafloor samples display abundant filamentous forms often resembling, in both size and shape, the twisted stalks of Gallionella and the elongated filaments of Leptothrix. Generally, these filamentous features are 1-5 microns in diameter and up to several microns in length. Some samples consist entirely of low- density, porous masses of silica encrusted filamentous forms. Presumably, these masses were formed by a rapid precipitation by the influx of silica-rich fluids into a microbial mat dominated by bacteria with filamentous morphologies. The presence of rare, amorphous (unmineralized) filamentous matter rich in C and Fe suggests that these bacteria were iron oxidizers. There is no evidence that sulfur oxidizers were present. Filamentous features sectioned by FIB milling show internal material within semi-hollow tubular-like features. Silica encrustations also show pseudo

  20. Chitosan-iron oxide nanocomposite based electrochemical aptasensor for determination of malathion.

    Science.gov (United States)

    Prabhakar, Nirmal; Thakur, Himkusha; Bharti, Anu; Kaur, Navpreet

    2016-10-01

    An electrochemical aptasensor based on chitosan-iron oxide nanocomposite (CHIT-IO) film deposited on fluorine tin Oxide (FTO) was developed for the detection of malathion. Iron oxide nanoparticles were prepared by co-precipitation method and characterized by Transmission electron microscopy and UV-Visible spectroscopy. The biotinylated DNA aptamer sequence specific to the malathion was immobilized onto the iron oxide doped-chitosan/FTO electrode by using streptavidin as linking molecule. Various characterization studies like Field Emission-Scanning Electron Microscopy (FE-SEM), Fourier Transform Infrared Spectroscopy (FT-IR), and Electrochemical studies were performed to attest the successful fabrication of bioelectrodes. Experimental parameters like aptamer concentration, response time, stability of electrode and reusability studies were optimized. Aptamer immobilized chitosan-iron oxide nanocomposite (APT/SA/CHIT-IO/FTO) bioelectrodes exhibited LOD of about 0.001 ng/mL within 15 min and spike-in studies revealed about 80-92% recovery of malathion from the lettuce leaves and soil sample.

  1. Reduction of molybdenum oxide from steelmaking slags by pure liquid iron

    Directory of Open Access Journals (Sweden)

    Gao Y.M.

    2012-01-01

    Full Text Available The effects of reaction temperature, slag basicity and FeO concentration on the reduction of molybdenum oxide from steelmaking slags by pure liquid iron were investigated experimently. The reduction kinetics of molybdenum oxide by liquid iron was analysed. The reaction models were developed based on the condition that diffusion of [Mo] in liquid iron and CaMoO4 in slag is the control steps, respectively. These reaction models were tested using data from a series of experiments. The results indicate that under the present experimental conditions, the temperature and the FeO content, other than slag basicity, have some effects on the reduction of molybdenum oxide from steelmaking slags by pure liquid iron. Both the molybdenum oxide reduction rate and final reduction ratio increase with an increase of temperature and a decrease of FeO content. The diffusion of CaMoO4 in slag which dominated overall reduction process is the only one ratecontrolling step with its apparent activation energy 294 kJ/mol. The reduction of molybdenum oxide used directly as alloy additive can be further enhanced by strong stirring in the converter practice.

  2. Oxidative stability of a heme iron-fortified bakery product: Effectiveness of ascorbyl palmitate and co-spray-drying of heme iron with calcium caseinate.

    Science.gov (United States)

    Alemán, Mercedes; Bou, Ricard; Tres, Alba; Polo, Javier; Codony, Rafael; Guardiola, Francesc

    2016-04-01

    Fortification of food products with iron is a common strategy to prevent or overcome iron deficiency. However, any form of iron is a pro-oxidant and its addition will cause off-flavours and reduce a product's shelf life. A highly bioavailable heme iron ingredient was selected to fortify a chocolate cream used to fill sandwich-type cookies. Two different strategies were assessed for avoiding the heme iron catalytic effect on lipid oxidation: ascorbyl palmitate addition and co-spray-drying of heme iron with calcium caseinate. Oxidation development and sensory acceptability were monitored in the cookies over one-year of storage at room temperature in the dark. The addition of ascorbyl palmitate provided protection against oxidation and loss of tocopherols and tocotrienols during the preparation of cookies. In general, ascorbyl palmitate, either alone or in combination with the co-spray-dried heme iron, prevented primary oxidation and hexanal formation during storage. The combination of both strategies resulted in cookies that were acceptable from a sensory point of view after 1year of storage.

  3. Wet hydrogen peroxide catalytic oxidation of phenol with FeAC (iron-embedded activated carbon) catalysts.

    Science.gov (United States)

    Liou, Rey-May; Chen, Shih-Hsiung; Huang, Cheng-Hsien; Hung, Mu-Ya; Chang, Jing-Song; Lai, Cheng-Lee

    2010-01-01

    This investigation aims at exploring the catalytic oxidation activity of iron-embedded activated carbon (FeAC) and the application for the degradation of phenol in the wet hydrogen peroxide catalytic oxidation (WHPCO). FeAC catalysts were prepared by pre-impregnating iron in coconut shell with various iron loadings in the range of 27.5 to 46.5% before they were activated. The FeAC catalysts were characterised by measuring their surface area, pore distribution, functional groups on the surface, and X-ray diffraction patterns. The effects of iron loading strongly inhibited the pore development of the catalyst but benefited the oxidation activity in WHPCO. It was found that the complete conversion of phenol was observed with all FeAC catalysts in oxidation. High level of chemical oxygen demand (COD) abatement can be achieved within the first 30 minutes of oxidation. The iron embedded in the activated carbon showed good performance in the degradation and mineralisation of phenol during the oxidation due to the active sites as iron oxides formed on the surface of the activated carbon. It was found that the embedding irons were presented in gamma-Fe(2)O(3), alpha-Fe(2)O(3), and alpha-FeCOOH forms on the activated carbon. The aging tests on FeAC catalysts showed less activity loss, and less iron leaching was found after four oxidation runs.

  4. On the kinetics of the initial oxidation of iron and iron nitride

    DEFF Research Database (Denmark)

    Graat, P.C.J.; Somers, Marcel A.J.; Mittemeijer, E.J.

    2002-01-01

    The initial oxidation of alfa-Fe and epsilon Fe2N1-x was investigated. Prior to oxidation the sample surfaces were either sputter cleaned with Ar+ ions or sputter cleaned followed by annealing. It was shown that the sputter cleaning pretreatment of epsilon Fe2N1-x led to a reduction of the N......), ellipsometry and high-resolution transmission electron microscopy (HREM). The oxidation kinetics, as determined with ellipsometry, were described theoretically with the model due to Fromhold and Cook, adopting time-dependent work functions of the metal-oxide and oxide-oxygen interfaces. The calculated...... the oxide film. For sputter-cleaned + annealed epsilon Fe2N1-x this lead to a nitrogen concentration larger than the maximum solubility of nitrogen in epsilon Fe2N1-x. The excess nitrogen at the metal-oxide interface, which is negatively charged as was indicated by the corresponding XPS N 1s peak, lead...

  5. Hydrogen production by ethanol partial oxidation over nano-iron oxide catalysts produced by chemical vapour synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Ahmed, Wael Ahmed Abou Taleb Sayed

    2011-01-13

    This work presents the experimental results of the synthesis of unsupported and supported SiC iron oxide nanoparticles and their catalytic activity towards ethanol partial oxidation. For comparison, further unsupported iron oxide phases were investigated towards the ethanol partial oxidation. These {gamma}-Fe{sub 2}O{sub 3} and {alpha}/{gamma}-Fe{sub 2}O{sub 3} phase catalysts were prepared by the CVS method using Fe(CO){sub 5} as precursor, supplied by another author. The {alpha}-Fe{sub 2}O{sub 3} and SiC nanoparticles were prepared by the CVS method using a home made hot wall reactor technique at atmospheric pressure. Ferrocene and tetramethylsilane were used as precursor for the production process. Process parameters of precursor evaporation temperature, precursor concentration, gas mixture velocity and gas mixture dilution were investigated and optimised to produce particle sizes in a range of 10 nm. For Fe{sub 2}O{sub 3}/SiC catalyst series production, a new hot wall reactor setup was used. The particles were produced by simultaneous thermal decomposition of ferrocene and tetramethylsilane in one reactor from both sides. The production parameters of inlet tube distance inside the reactor, precursor evaporation temperature and carrier gas flow were investigated to produce a series of samples with different iron oxide content. The prepared catalysts composition, physical and chemical properties were characterized by XRD, EDX, SEM, BET surface area, FTIR, XPS and dynamic light scattering (DLS) techniques. The catalytic activity for the ethanol gas-phase oxidation was investigated in a temperature range from 260 C to 290 C. The product distributions obtained over all catalysts were analysed with mass spectrometry analysis tool. The activity of bulk Fe{sub 2}O{sub 3} and SiC nanoparticles was compared with prepared nano-iron oxide phase catalysts. The reaction parameters, such as reaction temperature and O{sub 2}/ethanol ratio were investigated. The catalysts

  6. Physiological and Pathological Role of Alpha-Synuclein in Parkinson’s Disease through Iron Mediated Oxidative Stress; The Role of a Putative Iron-Responsive Element

    OpenAIRE

    David Olivares; Xudong Huang; Lars Branden; Greig, Nigel H.; Jack T. Rogers

    2009-01-01

    Parkinson’s disease (PD) is the second most common progressive neurodegenerative disorder after Alzheimer’s disease (AD) and represents a large health burden to society. Genetic and oxidative risk factors have been proposed as possible causes, but their relative contribution remains unclear. Dysfunction of alpha-synuclein (\\(\\alpha\\)-syn) has been associated with PD due to its increased presence, together with iron, in Lewy bodies. Brain oxidative damage caused by iron may be partly mediated ...

  7. Iron and Oxidative Stress in Parkinson's Disease: An Observational Study of Injury Biomarkers.

    Directory of Open Access Journals (Sweden)

    Marcio S Medeiros

    Full Text Available Parkinson's disease (PD is characterized by progressive motor impairment attributed to progressive loss of dopaminergic neurons in the substantia nigra (SN pars compacta. In addition to an accumulation of iron, there is also an increased production of reactive oxygen/nitrogen species (ROS/RNS and inflammatory markers. These observations suggest that iron dyshomeostasis may be playing a key role in neurodegeneration. However, the mechanisms underlying this metal-associated oxidative stress and neuronal damage have not been fully elucidated. To determine peripheral levels of iron, ferritin, and transferrin in PD patients and its possible relation with oxidative/nitrosative parameters, whilst attempting to identify a profile of peripheral biomarkers in this neurological condition. Forty PD patients and 46 controls were recruited to compare serum levels of iron, ferritin, transferrin, oxidative stress markers (superoxide dismutase (SOD, catalase (CAT, nitrosative stress marker (NOx, thiobarbituric acid reactive substances (TBARS, non-protein thiols (NPSH, advanced oxidation protein products (AOPP, ferric reducing ability of plasma (FRAP and vitamin C as well as inflammatory markers (NTPDases, ecto-5'-nucleotidase, adenosine deaminase (ADA, ischemic-modified albumin (IMA and myeloperoxidase. Iron levels were lower in PD patients, whereas there was no difference in ferritin and transferrin. Oxidative stress (TBARS and AOPP and inflammatory markers (NTPDases, IMA, and myeloperoxidase were significantly higher in PD, while antioxidants FRAP, vitamin C, and non-protein thiols were significantly lower in PD. The enzymes SOD, CAT, and ecto-5'-nucleotidase were not different among the groups, although NOx and ADA levels were significantly higher in the controls. Our data corroborate the idea that ROS/RNS production and neuroinflammation may dysregulate iron homeostasis and collaborate to reduce the periphery levels of this ion, contributing to alterations

  8. Iron and Oxidative Stress in Parkinson's Disease: An Observational Study of Injury Biomarkers.

    Science.gov (United States)

    Medeiros, Marcio S; Schumacher-Schuh, Arthur; Cardoso, Andreia Machado; Bochi, Guilherme Vargas; Baldissarelli, Jucimara; Kegler, Aline; Santana, Daniel; Chaves, Carolina Maria Martins Behle Soares; Schetinger, Maria Rosa Chitolina; Moresco, Rafael Noal; Rieder, Carlos R M; Fighera, Michele Rechia

    2016-01-01

    Parkinson's disease (PD) is characterized by progressive motor impairment attributed to progressive loss of dopaminergic neurons in the substantia nigra (SN) pars compacta. In addition to an accumulation of iron, there is also an increased production of reactive oxygen/nitrogen species (ROS/RNS) and inflammatory markers. These observations suggest that iron dyshomeostasis may be playing a key role in neurodegeneration. However, the mechanisms underlying this metal-associated oxidative stress and neuronal damage have not been fully elucidated. To determine peripheral levels of iron, ferritin, and transferrin in PD patients and its possible relation with oxidative/nitrosative parameters, whilst attempting to identify a profile of peripheral biomarkers in this neurological condition. Forty PD patients and 46 controls were recruited to compare serum levels of iron, ferritin, transferrin, oxidative stress markers (superoxide dismutase (SOD), catalase (CAT), nitrosative stress marker (NOx), thiobarbituric acid reactive substances (TBARS), non-protein thiols (NPSH), advanced oxidation protein products (AOPP), ferric reducing ability of plasma (FRAP) and vitamin C) as well as inflammatory markers (NTPDases, ecto-5'-nucleotidase, adenosine deaminase (ADA), ischemic-modified albumin (IMA) and myeloperoxidase). Iron levels were lower in PD patients, whereas there was no difference in ferritin and transferrin. Oxidative stress (TBARS and AOPP) and inflammatory markers (NTPDases, IMA, and myeloperoxidase) were significantly higher in PD, while antioxidants FRAP, vitamin C, and non-protein thiols were significantly lower in PD. The enzymes SOD, CAT, and ecto-5'-nucleotidase were not different among the groups, although NOx and ADA levels were significantly higher in the controls. Our data corroborate the idea that ROS/RNS production and neuroinflammation may dysregulate iron homeostasis and collaborate to reduce the periphery levels of this ion, contributing to alterations

  9. Effect of adsorbed polyaniline on the thermal stability of iron and arsenic oxides

    Directory of Open Access Journals (Sweden)

    Robson Fernandes de Farias

    2000-06-01

    Full Text Available Iron and arsenic oxide grains are coated with the conducting organic polymer polyaniline. The obtained samples were characterized by infrared spectroscopy, SEM, conducting measurements and thermogravimetry. The thermal stability of both oxides are increased. For As2O3 the sublimation temperature is increased from 165ºC in the pure oxide to 206ºC in the polymer modified sample. The pure Fe3O4 sample exhibits sublimation at 780ºC whereas the polyaniline coated oxide is stable until at least 1000ºC.

  10. Prebiotic Oxidative Polymerization of 2,3 Dimercaptopropanol on the Surface of Iron(III) Hydroxide Oxide

    Science.gov (United States)

    Weber, Arthur L.

    1994-01-01

    The oxidation of 2,3-Dimercapto-1-propanol by ferric ions on the surface of iron (III) hydroxide oxide yielded polydisulfide polymers. This polymerization occured readily at low dithiol concentration under mild aqueous conditions. Polydisulfide polymers up to the 15-mer were synthesized from 1 mM dithiol in 5 ml water reacted with iron (III) hydroxide oxide (20 mg, 160 micro mole Fe) for 3 days under anaerobic conditions at 40 C and pH 4. About 91% of the dithiol was converted to short soluble oligomers and 9% to insoluble larger oligomers that were isolated with the mineral phase. Reactions at higher dithiol concentrations with the same ratio of dithiol to mineral gave a higher yield of the larger insoluble oligomers. The relationship of these results to prebiotic polymer synthesis will be discussed.

  11. Prebiotic Polymerization: Oxidative Polymerization of 2,3 Dimercapto-1- Propanol on the Surface of Iron(III) Hydroxide Oxide

    Science.gov (United States)

    Weber, Arthur L.

    1995-01-01

    The oxidation of 2,3-dimercapto-1-propanol by ferric ions on the surface of iron(III) hydroxide oxide (Fe(OH)O) yielded polydisulfide oligomers. This polymerization occurred readily at low dithiol concentration under mild aqueous conditions. Polydisulfide polymers up to the 15-mer were synthesized from 1 mM dithiol in 5 ml water reacted with iron(III) hydroxide oxide (20 mg, 160 micromole Fe) for 3 days under anaerobic conditions at 40 C and pH 4. About 91% of the dithiol was converted to short soluble oligomers and 9% to insoluble larger oligomers that were isolated with the FE(OH)O phase. Reactions carried out at the same ratio of dithiol to FE(OH)O but at higher dithiol concentrations gave higher yields of the larger insoluble oligomers. The relationship of these results to prebiotic polymer synthesis is discussed.

  12. Prebiotic polymerization: Oxidative polymerization of 2, 3-dimercapto-1-propanol on the surface of iron(III) hydroxide oxide

    Science.gov (United States)

    Weber, Arthur L.

    1995-01-01

    The oxidation of 2, 3-dimercapto-1-propanol by ferric ions on the surface of iron(III) hydroxide oxide (Fe(OH)O) yielded polydisulfide oligomers. This polymerization occurred readily at low dithiol concentration under mild aqueous conditions. Polydisulfide polymers up to the 15-mer were synthesized from 1 mM dithiol in 5 ml water reacted with iron(III) hydroxide oxide (20 mg, 160 micromole Fe) for 3 days under anaerobic conditions at 40 C and pH 4. About 91% of the dithiol was converted to short soluble oligomers and 9% to insoluble larger oligomers that were isolated with the Fe(OH)O phase. Reactions carried out at the same ratio of dithiol to Fe(OH)O but at higher dithiol concentrations gave higher yields of the larger insoluble oligomers. The relationship of these results to prebiotic polymer synthesis is discussed.

  13. Early diagenetic quartz formation at a deep iron oxidation front in the Eastern Equatorial Pacific - A modern analogue for banded iron/chert formations?

    Science.gov (United States)

    Meister, Patrick; Chapligin, Bernhard; Picard, Aude; Meyer, Hanno; Fischer, Cornelius; Rettenwander, Daniel; Amthauer, Georg; Vogt, Christoph; Aiello, Ivano W.

    2014-07-01

    The mechanisms of early diagenetic quartz formation under low-temperature conditions are still poorly understood. In this study we investigated lithified cherts consisting of microcrystalline quartz recovered near the base of a 420 m thick Miocene-Holocene sequence of nannofossil and diatom ooze at a drill site in the Eastern Equatorial Pacific (Ocean Drilling Program Site 1226). Precipitation seems still ongoing based on a sharp depletion in dissolved silica at the depth of the cherts. Also, palaeo-temperatures reconstructed from δ18O values in the cherts are in the range of adjacent porewater temperatures. Opal-A dissolution appears to control silica concentration throughout the sequence, while the solution remains oversaturated with respect to quartz. However, at the depth of the sharp depletion in dissolved silica, quartz is still saturated while the more soluble silica phases are strongly undersaturated. Hence, precipitation of quartz was initiated by an auxiliary process. A process, previously observed to assist in the nucleation of quartz is the adsorption of silica on freshly precipitated iron oxides. Indeed, a deep iron oxidation front is present at 400 m below seafloor, which is caused by upward diffusing nitrate from an oxic seawater aquifer in the underlying oceanic crust. Sequential iron extraction showed a higher content of the adsorbed iron hydroxide fraction in the chert than in the adjacent nannofossil and diatom ooze. X-ray absorption near-edge structure (XANES) spectroscopy revealed that iron in the cherts predominantly occurs in illite and amorphous iron oxide, whereas iron in the nannofossil and diatom ooze occurs mainly in smectite. Mössbauer spectroscopy also indicated the presence of illite that is to 97% oxidized. Two possible mechanisms may be operative during early diagenetic chert formation at iron oxidation fronts: (1) silica precipitation is catalysed by adsorption to freshly precipitated iron oxide surfaces, and (2) porewater silica

  14. High temperature oxidation behavior of ODS iron-base alloys for nuclear energy application

    Energy Technology Data Exchange (ETDEWEB)

    Li, M.; Zhou, Z.; Liao, L.; Chen, W.; Ge, C. [Univ. of Science and Technology Beijing, School of Materials Science and Engineering, Beijing (China)

    2010-07-01

    Oxide dispersion strengthened (ODS) iron based alloys are considered as promising high temperature structural material for advanced nuclear energy systems due to its higher creep strength and radiation damage resistance than conventional commercial steels. In this study, the oxidation behavior of ODS iron based alloys with different Cr content (12-18%) was investigated by exposing samples at high temperature of 700℃ and 1000℃ in atmosphere environment, the exposure time is up to 500 h. Results showed that 14Cr and 18Cr ODS alloys exhibited better oxidation resistance than 12Cr ODS alloys. For the same chromium content, the oxidation resistance of ODS alloys are better than that of non-ODS alloys. (author)

  15. Widespread Iron Oxidizing Bacterial Communities in a late Paleoproterozoic Marine Environment

    Science.gov (United States)

    Planavsky, N.; Rouxel, O.; Bekker, A.

    2007-12-01

    Discovery of exceptionally well-preserved microfossils in the Gunflint Iron Formation provided the first evidence for diverse and abundant life in the Precambrian oceans. However, whether the Gunflint microbial communities were dominated by cyanobacteria or represent an archaic, lithotrophic ecosystem is a matter of longstanding debate. Here, we present Fe isotope and rare earth element (REE) data for microfossiliferous stromatolites that are consistent with the Gunflint biota being an iron-oxidizing bacterial community. The lack of or positive Ce anomalies in REE data indicate that the benthic community grew below a redoxcline and positive iron isotope compositions reveal that the microbial community only oxidized a fraction of the dissolved iron load. This depositional setting and Fe isotope evidence for incomplete iron oxidation are inconsistent with a cyanobacterial interpretation and provide strong support that the Gunflint biota was indeed a microaerophilic lithotrophic microbial ecosystem. An apparently restricted temporal distribution of the Gunflint biota coupled with a widespread spatial distribution signals a significant ecosystem evolutionary event in the late Paleoproterozoic when the ocean was redox-stratified and Fe-rich anoxic waters impinged onto the shallow shelf.

  16. Hydrous iron oxide modified diatomite as an active filtration medium for phosphate capture.

    Science.gov (United States)

    Wang, Zhe; Lin, Yan; Wu, Deyi; Kong, Hainan

    2016-02-01

    A simple method to functionalize diatomite with hydrous iron oxide was attempted and its performance as a new active filtration material to remove and recover phosphate from water was investigated under varying solution conditions. The Langmuir phosphate adsorption capacity increased from 0.6 mgP/g for raw diatomite to 4.89, 14.71, 25.02 mgP/g for hydrous iron oxide modified diatomite (HIOMD), depending on the amount of iron loaded. Loading of hydrous iron oxide caused the increase in true and bulk density and a decline in filtration rate, but to a lesser extent. It was shown that the HIOMD product with suitable iron content could retain a good filtration performance with a greatly increased adsorption capacity for phosphate. The phosphate adsorption increased by decreasing pH and by increasing ionic strength at high pH levels. The adsorption process was interpreted by ligand exchange. Coexisting oxyanions of sulfate, nitrate, citrate, carbonate, silicate and humic acid showed different effects on phosphate fixation but it was presumed that their influence at their concentrations and pH levels commonly encountered in effluent or natural waters was limited, i.e., HIOMD had a reasonably good selectivity. Results in repeated adsorption, desorption and regeneration experiment showed that the adsorbed phosphate could be recovered and the material could be reused after regeneration. The column test showed that HIOMD could be potentially utilized as an adsorption filtration medium for phosphate removal and recovery from water.

  17. What Oxidation State of Iron Determines the Amethyst Colour?

    Energy Technology Data Exchange (ETDEWEB)

    Dedushenko, S. K. [Moscow State University, Department of Chemistry (Russian Federation); Makhina, I. B.; Mar' in, A. A.; Mukhanov, V. A. [Russian Research Institute for Synthesis of Materials (Russian Federation); Perfiliev, Yu. D. [Moscow State University, Department of Chemistry (Russian Federation)

    2004-12-15

    A colourless quartz crystal doped with {sup 57}Fe{sup 3+} was obtained by hydrothermal synthesis in an NH{sub 4}F solution. The crystal was transformed into violet amethyst by gamma-irradiation. The change in colour was accompanied by changes in the Moessbauer spectrum that can be interpreted as the conversion of trivalent iron into the tetravalent state: Fe{sup 3+{yields}F}e{sup 4+}.

  18. Activatable molecular MRI nanoprobe for tumor cell imaging based on gadolinium oxide and iron oxide nanoparticle.

    Science.gov (United States)

    Li, Jingjing; Wang, Shan; Wu, Chen; Dai, Yue; Hou, Pingfu; Han, Cuiping; Xu, Kai

    2016-12-15

    Activatable molecular MRI nanoprobe for intracellular GSH sensing was designed. As an alternative to "always on" nanoprobe, activatable imaging nanoprobes which are designed to amplify or boost imaging signals only in response to the targets have attracted more and more attention. In this paper, we designed a novel activatable molecular magnetic resonance imaging (MRI) nanoprobe for tumor cell recognization based on a MRI signal variation induced by the distance change between T1 and T2 contrast agents (CAs) in the presence of glutathione (GSH). To achieve this aim, carboxyl group functionalized iron oxide nanoparticles (Fe3O4 NPs) and polyethylene glycol-coated gadolinium oxide (PEG-Gd2O3) NPs as T2 and T1 MRI CA were connected by cystamine which contains a disulfide linkage. Transmission electron microscopic (TEM), X-ray photoelectron spectroscopy (XPS), energy dispersive spectrometer (EDS), fourier transform infrared spectroscopy (FT-IR), mass spectra and (1)H nuclear magnetic resonance spectroscopy ((1)H NMR) were introduced for their characterizations. The formation of Fe3O4-cystamine-Gd2O3 (Fe3O4-SS-Gd2O3) nanocomplex resulted in a quenched T1 signal due to the near proximity of PEG-Gd2O3 NPs to Fe3O4 NPs and a "light-up" T1 signal with the cleavage of disulfide bond in the presence of GSH. These results provide not only an easy way to realize MRI of tumor cells based on the overexpressed intracellular GSH level, but also a new insight for the design of activatable MRI nanoprobe.

  19. Catalytic Degradation of Methylphosphonic Acid Using Iron Powder/Iron Oxides

    Science.gov (United States)

    2005-11-01

    aluminium/ aluminium oxide on the degradation of methylphosphonic acid (MPA), the final hydrolysis product of most nerve agents. EGA-FTIR provides... ALUMINIUM OXIDE ) UNDER AIR (BOTTOM). .................. 37 DSTO-TR-1849 1 1. Introduction The Convention on the Prohibition of the...as well as aluminium/ aluminium oxide , using temperature programmed EGA-FTIR. Since MPA is a Schedule II chemical the above requirement can only be

  20. Effects of iron oxidizing bacteria in thiourea leaching of gold ores

    OpenAIRE

    甲斐, 敬美; 山崎, 研市; 高橋, 武重; カイ, タカミ; ヤマサキ, ケンイチ; タカハシ, タケシゲ; KAI, Takami; YAMASAKI, Kenichi; Takahashi, Takeshige

    1991-01-01

    Bacterial leaching was combined with thiourea method for the gold leaching from ores. For gold bearing pyrites, biological pre-oxidation has been generally perfomed. In the present study, we carried out the biological treatment to the high silicate bearing ores by using the iron oxidizing bacteria, Thiobacillus ferrooxidans. The recovery of gold and silver was enhanced by the biological pretreatment, while the effects of the treatment was influenced by the types of gold ores. Since the biolog...

  1. Nanosized iron and iron–cobalt spinel oxides as catalysts for methanol decomposition

    OpenAIRE

    Manova, Elina; Tsoncheva, Tanya; Estournès, Claude; Paneva, Daniela; Tenchev, K.; Mitov, Ivan; Petrov, L.

    2006-01-01

    Nanosized iron and mixed iron–cobalt oxides supported on activated carbon materials and their bulk analogues prepared by thermal synthesis are studied by X-rays diffraction, Mo¨ssbauer spectroscopy, magnetic measurements and temperature programmed reduction. Their catalytic behavior in methanol decomposition to H2, CO and methane is tested. Phase transformations in the metal oxides affected by the reaction medium are also investigated. Changes in the reaction mechanism of the methanol decompo...

  2. Exacerbation of alcohol-induced oxidative stress in rats by polyunsaturated fatty acids and iron load

    Directory of Open Access Journals (Sweden)

    S N Patere

    2011-01-01

    Full Text Available The hypothesis that excessive intake of vegetable oil containing polyunsaturated fatty acids and iron load precipitate alcohol-induced liver damage was investigated in a rat model. In order to elucidate the mechanism underlying this synergism, the serum levels of iron, total protein, serum glutamate pyruvate transaminase, liver thiobarbituric acid reactive substances, and activities of antioxidant enzymes superoxide dismutase, catalase in liver of rats treated with alcohol, polyunsaturated fatty acids and iron per se and in combination were examined. Alcohol was fed to the rats at a level of 10-30% (blood alcohol was maintained between 150-350 mg/dl by using head space gas chromatography, polyunsaturated fatty acids at a level of 15% of diet and carbonyl iron 1.5-2% of diet per se and in combination to different groups for 30 days. Hepatotoxicity was assessed by measuring serum glutamate pyruvate transaminase, which was elevated and serum total protein, which was decreased significantly in rats fed with a combination of alcohol, polyunsaturated fatty acids and iron. It was also associated with increased lipid peroxidation and disruption of antioxidant defense in combination fed rats as compared to rats fed with alcohol or polyunsaturated fatty acids or iron. The present study revealed significant exacerbation of the alcohol-induced oxidative stress in presence of polyunsaturated fatty acids and iron.

  3. Infrared nanosecond pulsed laser irradiation of stainless steel: micro iron-oxide zones generation.

    Science.gov (United States)

    Ortiz-Morales, M; Frausto-Reyes, C; Soto-Bernal, J J; Acosta-Ortiz, S E; Gonzalez-Mota, R; Rosales-Candelas, I

    2014-07-15

    Nanosecond-pulsed, infrared (1064 nm) laser irradiation was used to create periodic metal oxide coatings on the surface of two samples of commercial stainless steel at ambient conditions. A pattern of four different metal oxide zones was created using a galvanometer scanning head and a focused laser beam over each sample. This pattern is related to traverse direction of the laser beam scanning. Energy-dispersive X-ray spectroscopy (EDS) was used to find the elemental composition and Raman spectroscopy to characterize each oxide zone. Pulsed laser irradiation modified the composition of the stainless steel samples, affecting the concentration of the main components within each heat affected zone. The Raman spectra of the generated oxides have different intensity profiles, which suggest different oxide phases such as magnetite and maghemite. In addition, these oxides are not sensible to the laser power of the Raman system, as are the iron oxide powders reported in the literature. These experiments show that it is possible to generate periodic patterns of various iron oxide zones by laser irradiation, of stainless steel at ambient conditions, and that Raman spectroscopy is a useful punctual technique for the analysis and inspection of small oxide areas.

  4. Iron Oxide Arrays Prepared from Ferrocene- and Silsesquioxane-Containing Block Copolymers

    Directory of Open Access Journals (Sweden)

    Raita Goseki

    2012-01-01

    Full Text Available Arrays of iron oxides as precursors of iron clusters were prepared by oxygen plasma treatment of block copolymer microphase-separated nanostructures in thin films. Block copolymers composed of ferrocene-containing and silsesquioxane-containing polymethacrylate (PMAPOSS-b-PMAHFC were successfully prepared, with different molecular weights and compositions and narrow molecular weight distributions, by living anionic polymerization. The formed microphase-separated nanostructures in the bulk were characterized by wide- and small-angle X-ray scattering (WAXS and SAXS, scanning electron microscopy (SEM, and transmission electron microscopy (TEM. Thin films were prepared from a solution of PMAPOSS-b-PMAHFC in tetrahydrofuran by spin coating onto silicon wafers. Fingerprint-type line nanostructures were formed in the PMAPOSS-b-PMAHFCs thin films after solvent annealing with carbon disulfide. Oxygen plasma treatment provided the final line arrays of iron oxides based on the formed nanostructural patterns.

  5. Iron oxide nanoparticles embedded in activated carbons prepared from hydrothermally treated waste biomass.

    Science.gov (United States)

    Hao, Wenming; Björkman, Eva; Yun, Yifeng; Lilliestråle, Malte; Hedin, Niklas

    2014-03-01

    Particles of iron oxide (Fe3O4 ; 20–40 nm) were embedded within activated carbons during the activation of hydrothermally carbonized (HTC) biomasses in a flow of CO2. Four different HTC biomass samples (horse manure, grass cuttings, beer production waste, and biosludge) were used as precursors for the activated carbons. Nanoparticles of iron oxide formed from iron catalyst included in the HTC biomasses. After systematic optimization, the activated carbons had specific surface areas of about 800 m2g1. The pore size distributions of the activated carbons depended strongly on the degree of carbonization of the precursors. Activated carbons prepared from highly carbonized precursors had mainly micropores, whereas those prepared from less carbonized precursors contained mainly mesopores. Given the strong magnetism of the activated carbon–nano-Fe3O4 composites, they could be particularly useful for water purification.

  6. Iron and its complexation by phenolic cellular metabolites: from oxidative stress to chemical weapons.

    Science.gov (United States)

    Chobot, Vladimir; Hadacek, Franz

    2010-01-01

    Iron is a transition metal that forms chelates and complexes with various organic compounds, also with phenolic plant secondary metabolites. The ligands of iron affect the redox potential of iron. Electrons may be transferred either to hydroxyl radicals, hydrogen peroxide or molecular oxygen. In the first case, oxidative stress is decreased, in the latter two cases, oxidative stress is increased. This milieu-dependent mode of action may explain the non-linear mode of action of juglone and other secondary metabolites. Attention to this phenomenon may help to explain idiosyncratic and often nonlinear effects that result in biological assays. Current chemical assays are discussed that help to explore these aspects of redox chemistry.

  7. H{sub 2} from biosyngas via iron reduction and oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Straus, J.; Terry, P. [H Power Corp., Belleville, NJ (United States)

    1995-09-01

    The production of hydrogen from the steam-oxidation of iron is a long-known phenomenon. The rise in interest in the production and storage of hydrogen justifies the examination of this process (and of the reverse process, the reduction of iron oxide) for commercial use. Under NREL subcontract ZAR-4-13294-02, a process simulation program was developed and used as a design tool to analyze various configurations of the iron-hydrogen purification/storage scheme. Specifically, analyses were performed to determine the effectiveness of this scheme in conjunction with biomass-derived gasified fuel streams (biosyngas). The results of the computer simulations led to a selection of a two-stage iron oxide reduction process incorporating interstage water and CO{sub 2} removal. Thermal analysis shows that the iron-hydrogen process would yield essentially the same quantity of clean hydrogen per unit of biomass as the conventional route. The iron-hydrogen process benefits from the excellent match potentially achievable between the otherwise-unusable energy fraction in the off-gas of the reduction reactor and the parasitic thermal, mechanical and electrical energy needs of some typical gasifier systems. The program simulations and economic analysis suggest that clean hydrogen from biomass feedstock could cost about 20% less via the iron-hydrogen method than by conventional methods of purification (using the same feedstock). Cost analyses show that lower capital costs would be incurred in generating clean hydrogen by utilizing this approach, especially in response to the fluctuating demand profile of a utility.

  8. LA-ICP-MS Allows Quantitative Microscopy of Europium-Doped Iron Oxide Nanoparticles and is a Possible Alternative to Ambiguous Prussian Blue Iron Staining.

    Science.gov (United States)

    Scharlach, Constantin; Müller, Larissa; Wagner, Susanne; Kobayashi, Yuske; Kratz, Harald; Ebert, Monika; Jakubowski, Norbert; Schellenberger, Eyk

    2016-05-01

    The development of iron oxide nanoparticles for biomedical applications requires accurate histological evaluation. Prussian blue iron staining is widely used but may be unspecific when tissues contain substantial endogenous iron. Here we tested whether microscopy by laser ablation coupled to inductively coupled plasma mass spectrometry (LA-ICP-MS) is sensitive enough to analyze accumulation of very small iron oxide particles (VSOP) doped with europium in tissue sections. For synthesis of VSOP, a fraction of Fe3+ (5 wt%) was replaced by Eu3+, resulting in particles with 0.66 mol% europium relative to iron (Eu-VSOP) but with otherwise similar properties as VSOP. Eu-VSOP or VSOP was intravenously injected into ApoE-/- mice on Western cholesterol diet and accumulated in atherosclerotic plaques of these animals. Prussian blue staining was positive for ApoE-/- mice with particle injection but also for controls. LA-ICP-MS microscopy resulted in sensitive and specific detection of the europium of Eu-VSOP in liver and atherosclerotic plaques. Furthermore, calibration with Eu-VSOP allowed calculation of iron and particle concentrations in tissue sections. The combination of europium-doped iron oxide particles and LA-ICP-MS microscopy provides a new tool for specific and quantitative analysis of particle distribution at the tissue level and allows correlation with other elements such as endogenous iron.

  9. Occurrence and activity of iron- and sulfur-oxidizing microorganisms in alkaline coal strip mine spoils.

    Science.gov (United States)

    Olson, G J; McFeters, G A; Temple, K L

    1981-03-01

    Spoils samples collected from a coal strip mine in southeastern Montana were examined for populations and activities of iron- and sulfur-oxidizing bacteria. Spoils examined were of three types: (a) acidic pyrite-rich waste coal, (b) oxidation halo material, and (c) alkaline material, which was the most widespread type. Bacterial numbers, sulfur oxidation, and(14)CO2 uptake activity declined to low levels in the summer when spoils were dry. Even in wetter spring months pyritic spoils contained relatively low numbers of acidophilic iron- and sulfur-oxidizing bacteria, probably indicative of water stress since the same spoils incubated with excess water or dilute mineral salts showed considerably greater bacterial numbers and activity. Certain wells in coal and spoils aquifers contained substantial populations of iron-oxidizing acidophilic bacteria. However, these wells were always of alkaline or neutral pH, indicating that bacterial pyrite oxidation occurred where groundwaters contacted either replaced spoils or coal that contained pyrite or other metal sulfides. Bacterial activity may contribute to trace metal and sulfate leaching in the area.

  10. The Oxidation of Iron: Experiment, Simulation, and Analysis in Introductory Chemistry

    Science.gov (United States)

    Schubert, Frederic E.

    2015-01-01

    In this exercise, an actual chemical reaction, oxidation of iron in air, is studied along with a related analogue simulation of that reaction. The rusting of steel wool is carried out as a class effort. The parallel simulation is performed by students working in small groups. The analogue for the reacting gas is a countable set of discrete marble…

  11. Expeditious organic–free assembly: morphologically controlled synthesis of iron oxides using microwaves

    Science.gov (United States)

    A microwave hydrothermal method is developed for the synthesis of iron oxides, α-Fe2O3, β-FeOOH, and the junction of α-Fe2O3–β-FeOOH. This method is absolutely organic-free, and various structures could be obtained simply by changing th...

  12. Synthesis of pseudopolyrotaxanes-coated Superparamagnetic Iron Oxide Nanoparticles as new MRI contrast agent

    NARCIS (Netherlands)

    Hosseini, F.; Panahifar, A.; Adeli, M.; Amiri, H.; Lascialfari, A.; Orsini, F.; Doschak, M.R.; Mahmoudi, M.

    2013-01-01

    Superparamagnetic Iron Oxide Nanoparticles (SPIONs) were synthesized and coated with pseudopolyrotaxanes (PPRs) and proposed as a novel hybrid nanostructure for medical imaging and drug delivery. PPRs were prepared by addition of alpha-cyclodextrin rings to functionalized polyethylene glycol (PEG) c

  13. Characterization of Iron Oxide Generated in Ruthner Plant of Pickling Unit in Mobarakeh Steel Complex

    Institute of Scientific and Technical Information of China (English)

    M.C.Amiri

    2003-01-01

    Reducing the chloride content in regenerated iron oxides (RIO) from steel-pickling acid waste economically treated by Ruthner process is the most critical issue for the development of RIO as a useful raw material resource. In this paper, the results of a new method for characterization and modification of RIO produced in Mobarakeh Steel Complex were reported.

  14. Neutrophilic Iron Oxidizing Bacteria: Occurrence and Relevance in Biological Drinking Water Treatment

    DEFF Research Database (Denmark)

    Gülay, Arda; Musovic, Sanin; Albrechtsen, Hans-Jørgen;

    Rapid sand filtration (RSF) is an economical way to treat anoxic groundwater around the world. It consists of groundwater aeration followed by passage through a sand filter. The oxidation and removal of ferrous iron, which is commonly found in anoxic groundwaters, is often believed to be a fully ...

  15. Neutrophilic iron-oxidizing bacteria: occurrence and relevance in biological drinking water treatment

    DEFF Research Database (Denmark)

    Gülay, Arda; Musovic, Sanin; Albrechtsen, Hans-Jørgen;

    2013-01-01

    Rapid sand filtration (RSF) is an economical way to treat anoxic groundwater around the world. It consists of groundwater aeration followed by passage through a sand filter. The oxidation and removal of ferrous iron, which is commonly found in anoxic groundwaters, is often believed to be a fully ...

  16. Iron oxide impregnated filter paper (Pi test): a review of its development and methodological research

    NARCIS (Netherlands)

    Chardon, W.J.; Menon, R.G.; Chien, S.H.

    1996-01-01

    Iron oxide impregnated filter paper (FeO paper) has been used to study the availability of phosphorus (P) to plants and algae, P desorption kinetics and P dynamics in the field. Since its initial development a number of differences in the method of preparation of the paper and its application have b

  17. Biocompatible Colloidal Suspensions Based on Magnetic Iron Oxide Nanoparticles: Synthesis, Characterization and Toxicological Profile

    Science.gov (United States)

    Coricovac, Dorina-Elena; Moacă, Elena-Alina; Pinzaru, Iulia; Cîtu, Cosmin; Soica, Codruta; Mihali, Ciprian-Valentin; Păcurariu, Cornelia; Tutelyan, Victor A.; Tsatsakis, Aristidis; Dehelean, Cristina-Adriana

    2017-01-01

    The use of magnetic iron oxide nanoparticles in biomedicine has evolved intensely in the recent years due to the multiple applications of these nanomaterials, mainly in domains like cancer. The aim of the present study was: (i) to develop biocompatible colloidal suspensions based on magnetic iron oxide nanoparticles as future theranostic tools for skin pathology and (ii) to test their effects in vitro on human keratinocytes (HaCat cells) and in vivo by employing an animal model of acute dermal toxicity. Biocompatible colloidal suspensions were obtained by coating the magnetic iron oxide nanoparticles resulted during the solution combustion synthesis with a double layer of oleic acid, as innovative procedure in increasing bioavailability. The colloidal suspensions were characterized in terms of dynamic light scattering (DLS) and transmission electron microscopy (TEM). The in vitro effects of these suspensions were tested by means of Alamar blue assay and the noxious effects at skin level were measured using non-invasive methods. The in vitro results indicated a lack of toxicity on normal human cells induced by the iron oxide nanoparticles colloidal suspensions after an exposure of 24 h to different concentrations (5, 10, and 25 μg·mL−1). The dermal acute toxicity test showed that the topical applications of the colloidal suspensions on female and male SKH-1 hairless mice were not associated with significant changes in the quality of barrier skin function.

  18. In-Situ Regeneration of Saturated Granular Activated Carbon by an Iron Oxide Nanocatalyst

    Science.gov (United States)

    Granular activated carbon (GAC) can remove trace organic pollutants and natural organic matter (NOM) from industrial and municipal waters. This paper evaluates an iron nanocatalyst approach, based on Fenton-like oxidation reactions, to regenerate spent GAC within a packed bed con...

  19. Endoscopic ultrasound guided injection of iron oxide magnetic nanoparticles for liver and pancreas

    DEFF Research Database (Denmark)

    Ungureanu, Bogdan Silviu; Pirici, Daniel; Margaritescu, Claudiu

    2016-01-01

    AIMS: Pancreatic cancer and hepatocellular carcinoma are two of the most aggressive types of cancer with limited therapeutic options in stages of advanced disease. Our objective is to assess the safety and feasibility of injecting iron oxide nanoparticles (IONs) via endoscopic ultrasound (EUS)-gu...

  20. Mineralized iron oxidizing bacteria from hydrothermal vents: targeting biosignatures on Mars

    Science.gov (United States)

    Leveille, R. J.

    2010-12-01

    Putative hydrothermal systems have been identified on Mars based on orbital imagery and rover-based analyses. Based on Earth analogs, hydrothermal systems on Mars would be highly attractive for their potential for preserving organic and inorganic biosignatures. For example, iron oxidizing bacteria are ubiquitous in marine and terrestrial hydrothermal systems, where they often display distinctive cell morphologies and are commonly encrusted by minerals, especially bacteriogenic iron oxides and silica. Microfossils of iron oxidizing bacteria have been found in ancient Si-Fe deposits and iron oxidation may be an ancient and widespread metabolic pathway. In order to investigate mineralized iron oxidizing bacteria as a biosignature, we have examined samples collected from extinct hydrothermal vents along Explorer Ridge, NE Pacific Ocean. In addition, microaerophilic iron oxidizing bacteria, isolated from active Pacific hydrothermal vents, were grown in a Fe-enriched seawater medium at constant pH (6.5) and O2 concentration (5%) in a controlled bioreactor system. Samples and experimental products were examined with a combination of variable-pressure and field-emission scanning electron microscopy (SEM), in some cases by preparing samples with a focused ion beam (FIB) milling system. Light-toned seafloor samples display abundant filamentous forms resembling, in both size and shape (1-5 microns in diameter and up to several microns in length), the twisted stalks of Gallionella and the elongated filaments of Leptothrix. Some samples consist entirely of low-density masses of silica (>90% Si) encrusted filamentous forms. The presence of unmineralized filamentous matter rich in C and Fe suggests that these are the remains of iron oxidizing bacteria. Mineralized filaments sectioned by FIB show variable internal material within semi-hollow, tubular-like features. Silica encrustations also show pseudo-concentric growth bands. In the bioreactor runs, abundant microbial growth and

  1. Conductive iron oxide minerals accelerate syntrophic cooperation in methanogenic benzoate degradation

    Energy Technology Data Exchange (ETDEWEB)

    Zhuang, Li; Tang, Jia; Wang, Yueqiang; Hu, Min; Zhou, Shungui, E-mail: sgzhou@soil.gd.cn

    2015-08-15

    Highlights: • Paddy soil contaminated with benzoate incubated with hematite and magnetite. • Iron oxides addition enhanced methanogenic benzoate degradation by 25–53%. • The facilitated syntrophy might involve direct interspecies electron transfer. • Bacillaceae, Peptococcaceae, and Methanobacterium are potentially involved. - Abstract: Recent studies have suggested that conductive iron oxide minerals can facilitate syntrophic metabolism of the methanogenic degradation of organic matter, such as ethanol, propionate and butyrate, in natural and engineered microbial ecosystems. This enhanced syntrophy involves direct interspecies electron transfer (DIET) powered by microorganisms exchanging metabolic electrons through electrically conductive minerals. Here, we evaluated the possibility that conductive iron oxides (hematite and magnetite) can stimulate the methanogenic degradation of benzoate, which is a common intermediate in the anaerobic metabolism of aromatic compounds. The results showed that 89–94% of the electrons released from benzoate oxidation were recovered in CH{sub 4} production, and acetate was identified as the only carbon-bearing intermediate during benzoate degradation. Compared with the iron-free controls, the rates of methanogenic benzoate degradation were enhanced by 25% and 53% in the presence of hematite and magnetite, respectively. This stimulatory effect probably resulted from DIET-mediated methanogenesis in which electrons transfer between syntrophic partners via conductive iron minerals. Phylogenetic analyses revealed that Bacillaceae, Peptococcaceae, and Methanobacterium are potentially involved in the functioning of syntrophic DIET. Considering the ubiquitous presence of iron minerals within soils and sediments, the findings of this study will increase the current understanding of the natural biological attenuation of aromatic hydrocarbons in anaerobic environments.

  2. Synthesis and characterization of L-carnosine coated iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Durmus, Z. [Department of Chemistry, Fatih University, B. Cekmece, 34500 Istanbul (Turkey); Kavas, H. [Department of Physics, Fatih University, B. Cekmece, 34500 Istanbul (Turkey); Baykal, A., E-mail: hbaykal@fatih.edu.tr [Department of Chemistry, Fatih University, B. Cekmece, 34500 Istanbul (Turkey); Sozeri, H. [TUBITAK-UME, National Metrology Institute, PO Box 54, 41470 Gebze-Kocaeli (Turkey); Alpsoy, L. [Department of Biology, Fatih University, B. Cekmece, 34500 Istanbul (Turkey); Celik, S.U. [Department of Chemistry, Fatih University, B. Cekmece, 34500 Istanbul (Turkey); Toprak, M.S. [Department of Functional Materials, Royal Institute of Technology, SE16440 Kista-Stockholm (Sweden)

    2011-02-03

    Research highlights: > L-Carnosine coated iron oxide nanoparticles (CCIO NPs) have been prepared via co-precipitation of Fe{sub 3}O{sub 4} (magnetite) in the presence of L-carnosine. > FTIR analysis showed that the binding of carnosine onto the surface of iron oxide is through unidentate linkage of carboxyl group. > Magnetization measurements revealed that L-carnosine iron oxide composite has immeasurable coercivity and remanence with absence of hysteritic behavior, which implies superparamagnetic behaviour at room temperature. > The synthesized amino acid-coated magnetic nanoparticles might be applied to cell separation, diagnosis and targeted drug delivery for cancer therapy. - Abstract: L-Carnosine coated iron oxide nanoparticles (CCIO NPs) have been prepared via co-precipitation of iron oxide in the presence of L-carnosine. Crystalline phase was identified as magnetite with an average crystallite size of 8 nm as estimated from X-ray line profile fitting. Particle size estimated from TEM by log-normal fitting was {approx}11 nm. FTIR analysis showed that the binding of carnosine onto the surface of iron oxide is through unidentate linkage of carboxyl group. CCIO NPs showed superparamagnetic charactersitic at room temperature. The magnetic core size of superparamagnetic CCIO NPs was found slightly smaller than the size obtained from TEM, due to the presence of magnetically dead layer. Magnetization measurements revealed that L-carnosine iron oxide composite has immeasurable coercivity and remanence with absence of hysteritic behavior, which implies superparamagnetic behavior at room temperature. The low value of saturation magnetization compared to the bulk magnetite has been explained by spin canting. LDH activity tests showed slight cytotoxicity of high dose of CCIO NPs. The ac conductivity of CCIO NPs was found to be greater than that of carnosine and the effective conduction mechanism was found as correlated barrier hopping (CBH). dc activation energy of the

  3. Tetrahydrocurcumin in combination with deferiprone attenuates hypertension, vascular dysfunction, baroreflex dysfunction, and oxidative stress in iron-overloaded mice.

    Science.gov (United States)

    Sangartit, Weerapon; Pakdeechote, Poungrat; Kukongviriyapan, Veerapol; Donpunha, Wanida; Shibahara, Shigeki; Kukongviriyapan, Upa

    2016-12-01

    Excessive iron can generate reactive oxygen species (ROS), leading to oxidative stress that is closely associated with cardiovascular dysfunction. Iron overload was induced in male ICR mice by injection of iron sucrose (10mg/kg/day) for eight weeks. Iron overload was evidenced by increased serum iron indices. The mice developed increased blood pressure, impaired vascular function and blunted response of the autonomic nervous system. These effects were accompanied by increased malondialdehyde levels in various tissues, increased nitric oxide metabolites in plasma and urine, and decreased blood glutathione. Tetrahydrocurcumin (THU, 50mg/kg/day), deferiprone (or L1, 50mg/kg/day) or both was orally administered throughout the period of iron sucrose injection. The treatments significantly alleviated the deleterious cardiovascular effects of iron overload, and were associated with modulation of nitric oxide levels. An imbalance between endothelial nitric oxide synthase (eNOS) and inducible NOS (iNOS) expression in response to iron overload was normalized by THU, L1 or the combination treatment. Moreover, the treatment decreased the upregulated expression levels of gp91(phox), p47(phox) and HO-1. The combination of THU and L1 exerted a greater effect than THU or L1 monotherapy. These results suggest beneficial effects of THU and L1 on iron-induced oxidative stress, hypertension, and vascular dysfunction.

  4. Increased endogenous DNA oxidation correlates to increased iron levels in melanocytes relative to keratinocytes.

    Science.gov (United States)

    Pelle, Edward; Huang, Xi; Zhang, Qi; Pernodet, Nadine; Yarosh, Daniel B; Frenkel, Krystyna

    2014-01-01

    The endogenous oxidative state of normal human epidermal melanocytes was investigated and compared to normal human epidermal keratinocytes (NHEKs) in order to gain new insight into melanocyte biology. Previously, we showed that NHEKs contain higher levels of hydrogen peroxide (H2O2) than melanocytes and that it can migrate from NHEKs to melanocytes by passive permeation. Nevertheless, despite lower concentrations of H2O2, we now report higher levels of oxidative DNA in melanocytes as indicated by increased levels of 8-oxo-2'-deoxyguanosine (8-oxo-dG): 4.49 (±0.55 SEM) 8-oxo-dG/10(6) dG compared to 1.49 (±0.11 SEM) 8-oxo-dG/10(6) dG for NHEKs. An antioxidant biomarker, glutathione (GSH), was also lower in melanocytes (3.14 nmoles (±0.15 SEM)/cell) in comparison to NHEKs (5.98 nmoles (±0.33 SEM)/cell). Intriguingly, cellular bioavailable iron as measured in ferritin was found to be nearly fourfold higher in melanocytes than in NHEKs. Further, ferritin levels in melanocytes were also higher than in hepatocarcinoma cells, an iron-rich cell, and it indicates that higher relative iron levels may be characteristic of melanocytes. To account for the increased oxidative DNA and lower GSH and H2O2 levels that we observe, we propose that iron may contribute to higher levels of oxidation by reacting with H2O2 through a Fenton reaction leading to the generation of DNA-reactive hydroxyl radicals. In conclusion, our data support the concept of elevated oxidation and high iron levels as normal parameters of melanocytic activity. We present new evidence that may contribute to our understanding of the melanogenic process and lead to the development of new skin care products.

  5. Biocompatibility of chitosan-coated iron oxide nanoparticles with osteoblast cells

    Directory of Open Access Journals (Sweden)

    Shi S

    2012-10-01

    Full Text Available Si-Feng Shi,1 Jing-Fu Jia,2 Xiao-Kui Guo,3 Ya-Ping Zhao,2 De-Sheng Chen,1 Yong-Yuan Guo,1 Tao Cheng,1 Xian-Long Zhang11Department of Orthopedic Surgery, Shanghai Sixth People’s Hospital, School of Medicine, 2School of Chemistry and Chemical Technology, 3Department of Medical Microbiology and Parasitology, School of Medicine, Shanghai Jiao Tong University Shanghai, ChinaBackground: Bone disorders (including osteoporosis, loosening of a prosthesis, and bone infections are of great concern to the medical community and are difficult to cure. Therapies are available to treat such diseases, but all have drawbacks and are not specifically targeted to the site of disease. Chitosan is widely used in the biomedical community, including for orthopedic applications. The aim of the present study was to coat chitosan onto iron oxide nanoparticles and to determine its effect on the proliferation and differentiation of osteoblasts.Methods: Nanoparticles were characterized using transmission electron microscopy, dynamic light scattering, x-ray diffraction, zeta potential, and vibrating sample magnetometry. Uptake of nanoparticles by osteoblasts was studied by transmission electron microscopy and Prussian blue staining. Viability and proliferation of osteoblasts were measured in the presence of uncoated iron oxide magnetic nanoparticles or those coated with chitosan. Lactate dehydrogenase, alkaline phosphatase, total protein synthesis, and extracellular calcium deposition was studied in the presence of the nanoparticles.Results: Chitosan-coated iron oxide nanoparticles enhanced osteoblast proliferation, decreased cell membrane damage, and promoted cell differentiation, as indicated by an increase in alkaline phosphatase and extracellular calcium deposition. Chitosan-coated iron oxide nanoparticles showed good compatibility with osteoblasts.Conclusion: Further research is necessary to optimize magnetic nanoparticles for the treatment of bone disease

  6. Solid-stabilized emulsion formation using stearoyl lactylate coated iron oxide nanoparticles

    Science.gov (United States)

    Vengsarkar, Pranav S.; Roberts, Christopher B.

    2014-10-01

    Iron oxide nanoparticles can exhibit highly tunable physicochemical properties that are extremely important in applications such as catalysis, biomedicine and environmental remediation. The small size of iron oxide nanoparticles can be used to stabilize oil-in-water Pickering emulsions due to their high energy of adsorption at the interface of oil droplets in water. The objective of this work is to investigate the effect of the primary particle characteristics and stabilizing agent chemistry on the stability of oil-in-water Pickering emulsions. Iron oxide nanoparticles were synthesized by the co-precipitation method using stoichiometric amounts of Fe2+ and Fe3+ salts. Sodium stearoyl lactylate (SSL), a Food and Drug Administration approved food additive, was used to functionalize the iron oxide nanoparticles. SSL is useful in the generation of fat-in-water emulsions due to its high hydrophilic-lipophilic balance and its bilayer-forming capacity. Generation of a monolayer or a bilayer coating on the nanoparticles was controlled through systematic changes in reagent concentrations. The coated particles were then characterized using various analytical techniques to determine their size, their crystal structure and surface functionalization. The capacity of these bilayer coated nanoparticles to stabilize oil-in-water emulsions under various salt concentrations and pH values was also systematically determined using various characterization techniques. This study successfully demonstrated the ability to synthesize iron oxide nanoparticles (20-40 nm) coated with SSL in order to generate stable Pickering emulsions that were pH-responsive and resistant to significant destabilization in a saline environment, thereby lending themselves to applications in advanced oil spill recovery and remediation.

  7. Development of a new aluminium matrix composite reinforced with iron oxide (Fe3O4

    Directory of Open Access Journals (Sweden)

    E. Bayraktar

    2010-01-01

    Full Text Available Purpose: of this paper is to develop new aluminium matrix (intermetallic composites reinforced with iron oxide (Fe3O4 that will be used in aeronautical engineering or in electronic industry. Different parameters such as sintering time and temperature, reinforcement, compact pressure were evaluated. The final purpose of this project is going on to improve conductivity and magnetic permeability of this new composite.Design/methodology/approach: In this paper, a new alternative materials “aluminium–iron oxide (Fe3O4, naturally as the mineral magnetite powder composite” has been developed by using a microwave (in the laboratory scale sintering programme with various aspect ratios, that iron oxide (Fe3O4 particle sizes and aluminium powders together were prepared. This paper contains partially preliminary results of our going-on research project.Findings: Green density increased regularly depending on the compact pressure and percentage of the iron oxide (Fe3O4. Micro and macro porosity was not found due to very clean microwave sintering. Density after microwave sintering was higher than that of traditional sintering in an electrical oven.Research limitations/implications: This project is going on and magnetic permeability and conductivity of this composite will be improved.Practical implications: This composite is new and clean and thanks to the new microwave sintering basically will be used in aeronautical engineering. Microwave heating results in lower energy costs and decreased processing times for many industrial processes.Originality/value: Originality of this paper is to use a new reinforcement in the aluminium matrix composite; Fe3O4-iron oxide. A new method - microwave sintering- has been carried out on this composite.

  8. Efficient oxidative dechlorination and aromatic ring cleavage of chlorinated phenols catalyzed by iron sulfophthalocyanine

    Energy Technology Data Exchange (ETDEWEB)

    Sorokin, A.; Meunier, B. [Laboratoire de Chimie de Coordination du CNRS, Toulouse (France); Seris, J.L. [Elf-Aquitaine, Artix (France)

    1995-05-26

    An efficient method has been developed for the catalytic oxidation of pollutants that are not easily degraded. The products of the hydrogen peroxide (H{sub 2}O{sub 2}) oxidation of 2,4,6-trichlorophenol (TCP) catalyzed by the iron complex 2,9,16,23-tetrasulfophthalocyanine (FePcS) were observed to be chloromaleic, chlorofumaric, maleic, and fumaric acids from dechlorination and aromatic cycle cleavage, as well as additional products that resulted from oxidative coupling. Quantitative analysis of the TCP oxidation reaction revealed that up to two chloride ions were released per TCP molecule. This chemical system, consisting of an environmentally safe oxidant (H{sub 2}O{sub 2}) and an easily accessible catalyst (FePcS), can perform several key steps in the oxidative mineralization of TCP, a paradigm of recalcitrant pollutants. 20 refs., 4 figs., 2 tabs.

  9. Investigation on the Thermal Crack Evolution and Oxidation Effect of Compacted Graphite Iron Under Thermal Shock

    Science.gov (United States)

    Wang, Xiaosong; Zhang, Weizheng; Guo, Bingbin

    2015-09-01

    For a better understanding of the thermal fatigue behavior in compacted graphite cast iron (CGI), the cyclic thermal shock test is carried out through alternating induction heating and water quenching. The optical and scanning electron microscopy observations are used to examine the cracks and oxidation behavior on the cross section and heating surface of the material specimen, respectively. The results show that the thermal cracks in CGI initiate at the graphite phases mostly, and the multi-sourced thermal cracks would result in stable cracks morphology finally through crack shielding effect. In the oxidation analysis, it is found that the oxidation of graphite is selective, and the graphite is the potential channels for oxygen diffusion from the outside into the matrix, resulting in local oxidation of matrix around graphite and continuous oxygen diffusion paths in the microstructure. Thermal cracks nucleate from the oxidation holes at graphite caused by decarburization, and they prefer to propagate and coalesce by penetrating the oxide bridges.

  10. In Situ Synchrotron Powder Diffraction Studies of Reduction-Oxidation (Redox) Behavior of Iron Ores and Ilmenite

    Science.gov (United States)

    Ilyushechkin, Alexander Y.; Kochanek, Mark; Tang, Liangguang; Lim, Seng

    2017-01-01

    Phase transformations of two types of iron-based oxides (iron ore and industrial-grade ilmenite) were studied using synchrotron powder diffraction of the samples processed in reducing and oxidizing atmospheres at 1173 K (900 °C) and 1223 K (950 °C), respectively. In iron ore oxidation, the disappearance of the wustite and fayalite phases was followed by hematite growth and a decrease of the magnetite phase. The magnetite phase was partially recovered by treatment in a reducing atmosphere. Ilmenite oxidation initiated decomposition of the ilmenite phase with rapid growth of hematite and gradual growth of the pseudobrookite phase. In a reducing atmosphere, ilmenite was gradually recovered from pseudobrookite with a relatively fast initial decrease in rutile and hematite content. Under reducing conditions, there was interaction of iron ore with magnesio-ferrites in iron ore-ash mixture and interaction of ilmenite with silica by the formation of fayalite.

  11. Iron Oxide Biominerals in Protein Nanocages, the Ferritins: Easing Into Life With Oxygen?

    Science.gov (United States)

    Theil, E. C.

    2008-12-01

    Organisms with ferritins could represent the progenitors of organisms that successfully made the transition to aerobic life. Ferritins are protein nanocages (8 or 12 nm diameter) that catalyze reactions between Fe(II) and O2 or H2O2 to synthesize ferrihydrite-like biominerals of Fe2O3(H2 O)n; phosphate is sometimes incorporated during mineralization. All groups of organisms, archea, bacteria, plants and animals have ferritins. Catalytic reactions between Fe and O occur in the protein cage with the products moving into the central protein cavity (5 or 8 nm diameter) where mineralization occurs; mineral sizes reach 4500 Fe with more than 7000 O atoms in the large cavities of maxi-ferritins and 500 Fe with more than 800 O atoms in the smaller, mini-ferritins, also called Dps proteins. H2O2 is preferentially used by mini-ferritins in archea and bacteria, contrasting with O2, preferentially used by maxi-ferritins in bacteria plants and animals, and some bacterial mini-ferritins that use either H2O2 or O2, to oxidize Fe(II) during biomineralization. The study of ferritins in contemporary organisms can illuminate mechanisms for oxygen and oxidant responses in changing environments now and in the past. Multiple genes encoding ferritins are often regulated by different environmental stimuli and in multi-cellular organisms, by tissue-specific, differentiation programs. The single celled E.coli has four ferritin genes, encoding three maxi-ferritins, one with a heme cofactor (bacterioferritin), and one mini-ferritin (Dps), expressed at different points in the culture cycle and/or in response to different stresses. Environmental iron, oxygen and peroxide all change the amounts of ferritin. When iron is plentiful, mineralized ferritin accumulates. Ferritin iron is recovered during periods of iron deficiency, apparently by selective unfolding of gated pores in ferritin protein nanocage that expose the mineral to reductants. Gene (DNA) transcription is the genetic target for iron

  12. Oligomerization of Glycine and Alanine Catalyzed by Iron Oxides: Implications for Prebiotic Chemistry

    Science.gov (United States)

    Shanker, Uma; Bhushan, Brij; Bhattacharjee, G.; Kamaluddin

    2012-02-01

    Iron oxide minerals are probable constituents of the sediments present in geothermal regions of the primitive earth. They might have adsorbed different organic monomers (amino acids, nucleotides etc.) and catalyzed polymerization processes leading to the formation of the first living cell. In the present work we tested the catalytic activity of three forms of iron oxides (Goethite, Akaganeite and Hematite) in the intermolecular condensation of each of the amino acids glycine and L-alanine. The effect of zinc oxide and titanium dioxide on the oligomerization has also been studied. Oligomerization studies were performed for 35 days at three different temperatures 50, 90 and 120°C without applying drying/wetting cycling. The products formed were characterized by HPLC and ESI-MS techniques. All three forms of iron oxides catalyzed peptide bond formation (23.2% of gly2 and 10.65% of ala2). The reaction was monitored every 7 days. Formation of peptides was observed to start after 7 days at 50°C. Maximum yield of peptides was found after 35 days at 90°C. Reaction at 120°C favors formation of diketopiperazine derivatives. It is also important to note that after 35 days of reaction, goethite produced dimer and trimer with the highest yield among the oxides tested. We suggest that the activity of goethite could probably be due to its high surface area and surface acidity.

  13. Synthesis of a red iron oxide/montmorillonite pigment in a CO2-rich brine solution.

    Science.gov (United States)

    Montes-Hernandez, G; Pironon, J; Villieras, F

    2006-11-15

    The homoionic calcium-montmorillonite was used to synthesize a red iron oxide/clay pigment in a CO2-rich brine solution (0.5 M of NaCl) by using an agitated batch-reactor (engineer autoclave). The operating conditions were 15 days of reaction, 200 bars of pressure and 150 degrees C of temperature. SEM/EDS, STEM/EDS, XRD and Infrared Spectrometry were performed to characterize before and after reaction the solid phase. The results showed the precipitation of spherical nanoparticles (50-500 nm) of iron oxide (Fe2O3) dispersed and/or coagulated in the clay-matrix. Evidently, this oxide produced red coloration in the final product. For this case, the Fe3+ cation was provided to the aqueous solution by the dissolution of Ca-montmorillonite, particularly, the dissolution of most fine particles contained in the starting clay material. The cation exchange process and precipitation of polymorph silica were also observed.

  14. Ultrafast electron and energy transfer in dye-sensitized iron oxide and oxyhydroxide nanoparticles

    DEFF Research Database (Denmark)

    Gilbert, Benjamin; Katz, Jordan E.; Huse, Nils

    2013-01-01

    –310 fs were found for all samples. Comparison between TA dynamics on uncoated and dye-sensitized hematite nanoparticles revealed the dye de-excitation pathway to consist of a competition between electron and energy transfer to the nanoparticles. We analyzed the TA data for hematite nanoparticles using...... a four-state model of the dye-sensitized system, finding electron and energy transfer to occur on the same ultrafast timescale. The interfacial electron transfer rates for iron oxides are very close to those previously reported for DCF-sensitized titanium dioxide (for which dye–oxide energy transfer...... photo-initiated interfacial electron transfer. This approach enables time-resolved study of the fate and mobility of electrons within the solid phase. However, complete analysis of the ultrafast processes following dye photoexcitation of the sensitized iron(iii) oxide nanoparticles has not been reported...

  15. Role of iron oxide impurities in electrocatalysis by multiwall carbon nanotubes: An investigation using a novel magnetically modified ITO electrodes

    Indian Academy of Sciences (India)

    Kanchan M Samant; Vrushali S Joshi; Kashinath R Patil; Santosh K Haram

    2014-04-01

    The role of iron oxide impurities in the electrocatalytic properties of multiwall carbon nanotubes (MWCNTs) prepared by catalytic chemical vapour decomposition method (CCVD) is studied in detail. A novel magnetically modified electrodes have been developed by which MWCNTs were immobilized on indium-tin oxide (ITO) electrodes, without any chemical binders. The electro-catalytic oxidation of dopamine, and reduction of hydrogen peroxide have been studied by cyclic voltammetry on magnetically modified electrodes with (i) MWCNTs with occluded iron oxide impurities (Fe-MWCNTs), (ii) MWCNTs grown on iron oxide nanoparticle particulate films (Io-MWCNTs) and (iii) pristine iron oxide nanoparticle particulate film (Io-NPs). A shift towards less positive potentials for the oxidation of dopamine was observed which is in the order of Fe-MWCNTs < Io-MWCNTs < Io-NPs. Similarly, trend towards less negative potentials for the reduction of hydrogen peroxide was observed. Thus, the electrocatalytic activities displayed by MWCNTs have been attributed to the iron oxide impurities associated with it. The systematic variation was related to the nature of interaction of iron oxide nanoparticles with MWCNT surface.

  16. Facile synthesis of iron oxides/reduced graphene oxide composites: application for electromagnetic wave absorption at high temperature

    Science.gov (United States)

    Zhang, Lili; Yu, Xinxin; Hu, Hongrui; Li, Yang; Wu, Mingzai; Wang, Zhongzhu; Li, Guang; Sun, Zhaoqi; Chen, Changle

    2015-03-01

    Iron oxides/reduced graphene oxide composites were synthesized by facile thermochemical reactions of graphite oxide and FeSO4.7H2O. By adjusting reaction temperature, α-Fe2O3/reduced graphene oxide and Fe3O4/reduced graphene oxide composites can be obtained conveniently. Graphene oxide and reduced graphene oxide sheets were demonstrated to regulate the phase transition from α-Fe2O3 to Fe3O4 via γ-Fe2O3, which was reported for the first time. The hydroxyl groups attached on the graphene oxide sheets and H2 gas generated during the annealing of graphene oxide are believed to play an important role during these phase transformations. These samples showed good electromagnetic wave absorption performance due to their electromagnetic complementary effect. These samples possess much better electromagnetic wave absorption properties than the mixture of separately prepared Fe3O4 with rGO, suggesting the crucial role of synthetic method in determining the product properties. Also, these samples perform much better than commercial absorbers. Most importantly, the great stability of these composites is highly advantageous for applications as electromagnetic wave absorption materials at high temperatures.

  17. Novel magnetically separable AgCl/iron oxide composites with enhanced photocatalytic activity driven by visible light

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Ying; Zhang, Yanrong, E-mail: yanrong_zhang@hust.edu.cn; Tan, Jue

    2013-10-15

    Highlights: •The AgCl/iron oxide composites were prepared by a chemical precipitation method. •The composites exhibited improved performances in the photodegradation of pollutants. •The visible light photocatalysts could be recycled easily by a magnet. -- Abstract: In this work, AgCl/iron oxide composites were synthesized by a simple chemical precipitation method and calcining process. The composition of the material and magnetic and optical properties of the composites were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and vibrating specimen magnetometer (VSM) techniques, which confirms the high crystalline and magnetic behavior of the composites. UV-vis diffuse reflectance spectral (DRS) studies showed that the AgCl/iron oxide composites were of much higher absorption in longer wavelength region compared to bare iron oxide. The AgCl/iron oxide composites showed better performance in the photodegradation of organic dyes Rhodamin B (RhB) under the fluorescent lamp irradiation, which is remarkably superior to the N-TiO{sub 2}. The degradation of microcystin-LR (MC-LR) and phenol was also found to be good owing to its effective electron-hole separation at AgCl/iron oxide interface. The separation of AgCl/iron oxide composites from the treated water was achieved by an external magnetic field as γ-Fe{sub 2}O{sub 3} exhibits enough magnetic power to facilitate the separation.

  18. Preparation and evaluation of poly(2-hydroxyethyl aspartamide)-hexadecylamine-iron oxide for MR imaging of lymph nodes

    Science.gov (United States)

    Ha, Dae Chul; Lee, Ha Young; Son, Yeo Won; Yuk, Soon Hong; Choi, Youn Woong; Kwak, Byung Kook; Shin, Byung Cheol; Cho, Cheong-Weon; Cho, Sun Hang

    2014-01-01

    The purpose of this study was to synthesize biocompatible poly(2-hydroxyethyl aspartamide)-C16-iron oxide (PHEA-C16-iron oxide) nanoparticles and to evaluate their efficacy as a contrast agent for magnetic resonance imaging of lymph nodes. The PHEA-C16-iron oxide nanoparticles were synthesized by coprecipitation method. The core size of the PHEA-C16-iron oxide nanoparticles was about 5 to 7 nm, and the overall size of the nanoparticles was around 20, 60, and 150 nm in aqueous solution. The size of the nanoparticles was controlled by the amount of C16. The 3.0-T MRI signal intensity of a rabbit lymph node was effectively reduced after intravenous administration of PHEA-C16-iron oxide with the size of 20 nm. The in vitro and in vivo toxicity tests revealed the high biocompatibility of PHEA-C16-iron oxide nanoparticles. Therefore, PHEA-C16-iron oxide nanoparticles with 20-nm size can be potentially useful as T2-weighted MR imaging contrast agents for the detection of lymph nodes.

  19. Glycol chitosan/heparin immobilized iron oxide nanoparticles with a tumor-targeting characteristic for magnetic resonance imaging.

    Science.gov (United States)

    Yuk, Soon Hong; Oh, Keun Sang; Cho, Sun Hang; Lee, Beom Suk; Kim, Sang Yoon; Kwak, Byung-Kook; Kim, Kwangmeyung; Kwon, Ick Chan

    2011-06-13

    We described the preparation of the glycol chitosan/heparin immobilized iron oxide nanoparticles (composite NPs) as a magnetic resonance imaging agent with a tumor-targeting characteristic. The iron oxide nanoseeds used clinically as a magnetic resonance imaging agent were immobilized into the glycol chitosan/heparin network to form the composite NPs. To induce the ionic interaction between the iron oxide nanoseeds and glycol chitosan, gold was deposited on the surface of iron oxide nanoseeds. After the immobilization of gold-deposited iron oxide NPs into the glycol chitosan network, the NPs were stabilized with heparin based on the ionic interaction between cationic glycol chitosan and anionic heparin. FE-SEM (field emission-scanning electron microscopy) and a particle size analyzer were used to observe the formation of the stabilized composite NPs, and a Jobin-Yvon Ultima-C inductively coupled plasma-atomic emission spectrometer (ICP-AES) was used to measure the contents (%) of formed iron oxide nanoseeds as a function of reaction temperature and formed gold deposited on the iron oxide nanoparticles. We also evaluated the time-dependent excretion profile, in vivo biodistribution, circulation time, and tumor-targeting ability of the composite NPs using a noninvasive NIR fluorescence imaging technology. To observe the MRI contrast characteristic, the composite NPs were injected into the tail veins of tumor-bearing mice to demonstrate their selective tumoral distribution. The MR images were collected with conventional T(2)-weighted spin echo acquisition parameters.

  20. Pyrene Removal from Contaminated Soils by Modified Fenton Oxidation Using Iron Nano Particles

    Directory of Open Access Journals (Sweden)

    Sahand Jorfi

    2013-07-01

    Full Text Available Background:The problems related to conventional Fenton oxidation, including low pH required and production of considerable amounts of sludge have led researchers to investigate chelating agents which might improve the operating range of pH and the use of nano iron particle to reduce the excess sludge. The pyrene removal from contaminated soils by modified Fenton oxidation at neutral pH was defined as the main objective of the current study.Methods:Varying concentrations of H2O2 (0-500 mM and iron nano oxide (0-60 mM, reaction times of 0.5-24 hours and variety of chelating agents including sodium pyrophosphate, sodium citrate, ethylene diamine tetraacetic, fulvic and humic acid were all investigated at pyrene concentration levels of 100 – 500 mg/kg.Results:By applying the following conditions (H2O2 concentration of 300 mM, iron nano oxide of 30 mM, sodium pyrophosphate as chelating agent, pH 3 and reaction time of 6 hours the pyrene removal efficiency at an initial concentration of 100 mg/kg was found to be 99%. As a result, the pyrene concentration was reduced from 100 to 93 mg/kg once the above optimum conditions are met.Conclusions:In this research, the modified Fenton oxidation using iron nano oxide at optimum conditions is introduced as an efficient alternative method in lab scale for chemical remediation or pre-treatment of soils contaminated by pyrene at neutral pH.

  1. Authigenic iron oxide formation in the estuarine mixing zone of the Yangtze River

    Science.gov (United States)

    Fan, D. J.; Neuser, R. D.; Sun, X. G.; Yang, Z. S.; Guo, Z. G.; Zhai, S. K.

    2008-02-01

    Estuaries are elementary geochemical fronts where river water and seawater mix. Within this mixing zone, iron and other non-conservative elements can undergo complex reactions to form new solid phases. In order to understand authigenic iron oxide formation in the Yangtze River Estuary, two onsite water-mixing sets of experiments were conducted, one by mixing variable amounts of unfiltered Yangtze River water with filtered East China Sea water of different salinity (set 1), the other by mixing variable amounts of filtered Yangtze River water with filtered East China Sea water of different salinity (set 2). In set 2, the minerals newly formed in the course of mixing were investigated by means of a scanning electron microscope fitted with an energy-dispersive X-ray analytical system. It was found that ferrihydrite and lepidocrocite were formed in these mixing experiments, coexisting in nearly equal amounts. These iron oxides appear as aggregated particles with a large grain-size range of several microns to more than 100 μm. The electrolytic properties of seawater played an important role in the formation of these authigenic iron oxides. Kaolinite and organic aggregates were also found in the experimentally mixed pre-filtered waters. Amounts of newly formed suspended matter (set 2) were one to three orders of magnitude lower than those of total suspended matter (TSM) (set 1). This implies that newly formed minerals represent only a very small proportion of TSM in the estuarine mixing zone of the Yangtze River.

  2. Synthesis of iron oxide nanoparticles of narrow size distribution on polysaccharide templates

    Indian Academy of Sciences (India)

    M Nidhin; R Indumathy; K J Sreeram; Balachandran Unni Nair

    2008-02-01

    We report here the preparation of nanoparticles of iron oxide in the presence of polysaccharide templates. Interaction between iron (II) sulfate and template has been carried out in aqueous phase, followed by the selective and controlled removal of the template to achieve narrow distribution of particle size. Particles of iron oxide obtained have been characterized for their stability in solvent media, size, size distribution and crystallinity and found that when the negative value of the zeta potential increases, particle size decreases. A narrow particle size distribution with 100 = 275 nm was obtained with chitosan and starch templates. SEM measurements further confirm the particle size measurement. Diffuse reflectance UV–vis spectra values show that the template is completely removed from the final iron oxide particles and powder XRD measurements show that the peaks of the diffractogram are in agreement with the theoretical data of hematite. The salient observations of our study shows that there occurs a direct correlation between zeta potential, polydispersity index, bandgap energy and particle size. The crystallite size of the particles was found to be 30–35 nm. A large negative zeta potential was found to be advantageous for achieving lower particle sizes, owing to the particles remaining discrete without agglomeration.

  3. In situ reduction of as-prepared γ-Iron Oxide Nanoparticles

    DEFF Research Database (Denmark)

    Garbus, Pelle Gorm; Ahlburg, Jakob; Christensen, Mogens

    .L., et al., Size and Size Distribution Control of γ-Fe2O3 Nanocrystallites: An in Situ Study. Crystal Growth & Design, 2014. 14(3): p. 1307-1313.3.Bondesgaard, M., et al., Guide to by-products formed in organic solvents under solvothermal conditions. The Journal of Supercritical Fluids, 2016. 113: p. 166...... behind the structural development [1, 2] adds to the fundamental understanding of materials’ formation and can lead to new synthesis pathways. In this study, iron oxide (γ-Fe2O3) particles were heated to 400°C under a flow of H2/Ar mixture, while the process was followed by in situ synchrotron powder X......-iron oxide Fe2O3. The reduction of maghemite to body centered cubic (BCC) iron does not go through a detectable intermediate state.1.Jensen, K.M., et al., Mechanisms for iron oxide formation under hydrothermal conditions: an in situ total scattering study. ACS nano, 2014. 8(10): p. 10704-10714.2.Andersen, H...

  4. Adsorption of zinc ions from water using zeolite/iron oxide composites

    Energy Technology Data Exchange (ETDEWEB)

    Fungaro, D.A.; Graciano, J.E.A. [Institute for Energy and Nuclear Research, Sao Paulo (Brazil)

    2007-07-01

    The adsorption characteristics of zeolites synthesized from fly ash were combined in a composite with the magnetic properties of iron oxides to produce adsorbents which were magnetic materials. Such zeolite/iron oxide magnetic composites were prepared with weight ratios of 3:1, 2:1 and 1:1. The experimental data for the equilibrium adsorption isotherms of Zn{sup 2+} ions onto the composites were modelled using the Freundlich and Langmuir equations. The presence of iron oxide had no significant effect on the adsorption capacities of the magnetic composites. The experimental data were also employed to determine the kinetic characteristics of the adsorption process. The adsorption of Zn{sup 2+} ions was found to follow pseudo-second-order type kinetics. Although intra-particle diffusion occurred in the adsorption processes, it could not be accepted as the primary rate-determining step. The evaluated thermodynamic parameters indicated that the adsorption of Zn{sup 2+} ions onto zeolite/iron composites was spontaneous and endothermic.

  5. Antibacterial activity of magnetic iron oxide nanoparticles synthesized by laser ablation in liquid

    Energy Technology Data Exchange (ETDEWEB)

    Ismail, Raid A., E-mail: raidismail@yahoo.com [Laser Physics Division, Applied Science Department, University of Technology, Baghdad (Iraq); Sulaiman, Ghassan M. [Biotechnology Division, Applied Science Department, University of Technology, Baghdad (Iraq); Abdulrahman, Safa A. [Laser Physics Division, Applied Science Department, University of Technology, Baghdad (Iraq); Marzoog, Thorria R. [Biotechnology Division, Applied Science Department, University of Technology, Baghdad (Iraq)

    2015-08-01

    In this study, (50–110 nm) magnetic iron oxide (α-Fe{sub 2}O{sub 3}) nanoparticles were synthesized by pulsed laser ablation of iron target in dimethylformamide (DMF) and sodium dodecyl sulfate (SDS) solutions. The structural properties of the synthesized nanoparticles were investigated by using Fourier Transform Infrared (FT-IR) spectroscopy, UV–VIS absorption, scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray diffraction (XRD). The effect of laser fluence on the characteristics of these nanoparticles was studied. Antibacterial activities of iron oxide nanoparticles were tested against Gram-positive; Staphylococcus aureus and Gram-negative; Escherichia coli, Pseudomonas aeruginosa and Serratia marcescens. The results showed a noteworthy inhibition on both bacterial strains. The preparation conditions were found to affect significantly the antibacterial activity of these nanoparticles. The synthesized magnetic nanoparticles were used to capture rapidly S. aureus bacteria under the magnetic field effect. - Highlights: • Synthesis magnetic iron oxide nanoparticles by pulsed laser ablation • Antibacterial activity against Gram-positive and Gram-negative bacteria • Captured magnetic nanoparticles by S. aureus bacteria under effect of magnetic field.

  6. Grafting of diazonium salts on oxides surface: formation of aryl-O bonds on iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Brymora, Katarzyna [LUNAM Université du Maine, IMMM UMR CNRS 6283 (France); Fouineau, Jonathan; Eddarir, Asma; Chau, François [Université Paris Diderot, Sorbonne Paris Cité, ITODYS CNRS UMR 7086 (France); Yaacoub, Nader; Grenèche, Jean-Marc [LUNAM Université du Maine, IMMM UMR CNRS 6283 (France); Pinson, Jean; Ammar, Souad [Université Paris Diderot, Sorbonne Paris Cité, ITODYS CNRS UMR 7086 (France); Calvayrac, Florent, E-mail: florent.calvayrac@univ-lemans.fr [LUNAM Université du Maine, IMMM UMR CNRS 6283 (France)

    2015-11-15

    Combining ab initio modeling and {sup 57}Fe Mössbauer spectrometry, we characterized the nature of the chemical linkage of aminoalkyl arenediazonium salt on the surface of iron oxide nanoparticles. We established that it is built through a metal–oxygen–carbon bonding and not a metal–carbon one, as usually suggested and commonly observed in previously studied metal- or carbon-based surfaces.

  7. The influence of thermal annealing on structure and oxidation of iron nanowires

    Directory of Open Access Journals (Sweden)

    Krajewski Marcin

    2015-03-01

    Full Text Available Raman spectroscopy as well as Mössbauer spectroscopy were applied in order to study the phase composition of iron nanowires and its changes, caused by annealing in a neutral atmosphere at several temperatures ranging from 200°C to 800°C. As-prepared nanowires were manufactured via a simple chemical reduction in an external magnetic field. Both experimental techniques proved formation of the surface layer covered by crystalline iron oxides, with phase composition dependent on the annealing temperature (Ta. At higher Ta, hematite was the dominant phase in the nanowires.

  8. Investigation of Iron Oxide Morphology in a Cyclic Redox Water Splitting Process for Hydrogen Generation

    Directory of Open Access Journals (Sweden)

    Michael M. Bobek

    2012-10-01

    Full Text Available A solar fuels generation research program is focused on hydrogen production by means of reactive metal water splitting in a cyclic iron-based redox process. Iron-based oxides are explored as an intermediary reactive material to dissociate water molecules at significantly reduced thermal energies. With a goal of studying the resulting oxide chemistry and morphology, chemical assistance via CO is used to complete the redox cycle. In order to exploit the unique characteristics of highly reactive materials at the solar reactor scale, a monolithic laboratory scale reactor has been designed to explore the redox cycle at temperatures ranging from 675 to 875 K. Using high resolution scanning electron microscope (SEM and electron dispersive X-ray spectroscopy (EDS, the oxide morphology and the oxide state are quantified, including spatial distributions. These images show the change of the oxide layers directly after oxidation and after reduction. The findings show a significant non-stoichiometric O/Fe gradient in the atomic ratio following oxidation, which is consistent with a previous kinetics model, and a relatively constant, non-stoichiometric O/Fe atomic ratio following reduction.

  9. Toxicity assessment and comparison between two types of iron oxide nanoparticles in Mytilus galloprovincialis

    Energy Technology Data Exchange (ETDEWEB)

    Taze, Chrysa; Panetas, Ioannis [Laboratory of Animal Physiology, Department of Zoology, School of Biology, Aristotle University of Thessaloniki, 54124 Thessaloniki (Greece); Kalogiannis, Stavros [Alexander Technological Educational Institution of Thessaloniki, Department of Nutrition and Dietetics, Thessaloniki (Greece); Feidantsis, Konstantinos [Laboratory of Animal Physiology, Department of Zoology, School of Biology, Aristotle University of Thessaloniki, 54124 Thessaloniki (Greece); Gallios, George P. [Laboratory of General & Inorganic Chemical Technology, School of Chemistry, Aristotle University, GR-54124 Thessaloniki (Greece); Kastrinaki, Georgia [Aerosol & Particle Technology Laboratory, CERTH/CPERI, P.O. Box 60361, 57001 Thessaloniki (Greece); Konstandopoulos, Athanasios G. [Aerosol & Particle Technology Laboratory, CERTH/CPERI, P.O. Box 60361, 57001 Thessaloniki (Greece); Department of Chemical Engineering, Aristotle University, PO. Box 1517, 54006 Thessaloniki (Greece); Václavíková, Miroslava; Ivanicova, Lucia [Institute of Geotechnics, Slovak Academy of Sciences, Watsonova 45, SK-04001 Kosice (Slovakia); Kaloyianni, Martha, E-mail: kaloyian@bio.auth.gr [Laboratory of Animal Physiology, Department of Zoology, School of Biology, Aristotle University of Thessaloniki, 54124 Thessaloniki (Greece)

    2016-03-15

    Highlights: • The impact of two types of iron oxide nanoparticles on the physiological status of mussels was studied. • Oxidative parameters significantly changed after 1, 3, 7 days of exposure. • The nanoparticles induced oxidative stress to the animals. • All the parameters measured could be applied in biomonitoring studies. - Abstract: Nanoparticles (NPs), due to their increased application and production, are being released into the environment with unpredictable impact on the physiology of marine organisms, as well as on entire ecosystems and upcoming effects on human health. The aim of the present study was to evaluate and compare the oxidative responses of the mussel Mytilus galloprovincialis after exposure to iron oxide NPs and to iron oxide NPs incorporated into zeolite for 1, 3 and 7 days. Our results showed that both effectors induced changes on animal physiology by causing oxidative stress in hemocytes of exposed mussels compared to control animals. This was shown by the significant increase in reactive oxygen species (ROS) production, protein carbonylation, lipid peroxidation, ubiquitin conjugates and DNA damage. In addition an increase in prooxidant levels as measured by the prooxidant-antioxidant balance (PAB) assay was observed in exposed mussels’ hemolymph. The results show that ROS, DNA damage, protein and lipid oxidation, ubiquitin conjugates and PAB could constitute, after further investigation, reliable biomarkers for the evaluation of pollution or other environmental stressors. In addition, more studies are needed in order to ensure the safety of these NPs on various biomedical applications, since it is critical to design NPs that they meet the demands of application without causing cellular toxicity.

  10. Two kinds of ferritin protect ixodid ticks from iron overload and consequent oxidative stress.

    Science.gov (United States)

    Galay, Remil Linggatong; Umemiya-Shirafuji, Rika; Bacolod, Eugene T; Maeda, Hiroki; Kusakisako, Kodai; Koyama, Jiro; Tsuji, Naotoshi; Mochizuki, Masami; Fujisaki, Kozo; Tanaka, Tetsuya

    2014-01-01

    Ticks are obligate hematophagous parasites that have successfully developed counteractive means against their hosts' immune and hemostatic mechanisms, but their ability to cope with potentially toxic molecules in the blood remains unclear. Iron is important in various physiological processes but can be toxic to living cells when in excess. We previously reported that the hard tick Haemaphysalis longicornis has an intracellular (HlFER1) and a secretory (HlFER2) ferritin, and both are crucial in successful blood feeding and reproduction. Ferritin gene silencing by RNA interference caused reduced feeding capacity, low body weight and high mortality after blood meal, decreased fecundity and morphological abnormalities in the midgut cells. Similar findings were also previously reported after silencing of ferritin genes in another hard tick, Ixodes ricinus. Here we demonstrated the role of ferritin in protecting the hard ticks from oxidative stress. Evaluation of oxidative stress in Hlfer-silenced ticks was performed after blood feeding or injection of ferric ammonium citrate (FAC) through detection of the lipid peroxidation product, malondialdehyde (MDA) and protein oxidation product, protein carbonyl. FAC injection in Hlfer-silenced ticks resulted in high mortality. Higher levels of MDA and protein carbonyl were detected in Hlfer-silenced ticks compared to Luciferase-injected (control) ticks both after blood feeding and FAC injection. Ferric iron accumulation demonstrated by increased staining on native HlFER was observed from 72 h after iron injection in both the whole tick and the midgut. Furthermore, weak iron staining was observed after Hlfer knockdown. Taken together, these results show that tick ferritins are crucial antioxidant molecules that protect the hard tick from iron-mediated oxidative stress during blood feeding.

  11. Two kinds of ferritin protect ixodid ticks from iron overload and consequent oxidative stress.

    Directory of Open Access Journals (Sweden)

    Remil Linggatong Galay

    Full Text Available Ticks are obligate hematophagous parasites that have successfully developed counteractive means against their hosts' immune and hemostatic mechanisms, but their ability to cope with potentially toxic molecules in the blood remains unclear. Iron is important in various physiological processes but can be toxic to living cells when in excess. We previously reported that the hard tick Haemaphysalis longicornis has an intracellular (HlFER1 and a secretory (HlFER2 ferritin, and both are crucial in successful blood feeding and reproduction. Ferritin gene silencing by RNA interference caused reduced feeding capacity, low body weight and high mortality after blood meal, decreased fecundity and morphological abnormalities in the midgut cells. Similar findings were also previously reported after silencing of ferritin genes in another hard tick, Ixodes ricinus. Here we demonstrated the role of ferritin in protecting the hard ticks from oxidative stress. Evaluation of oxidative stress in Hlfer-silenced ticks was performed after blood feeding or injection of ferric ammonium citrate (FAC through detection of the lipid peroxidation product, malondialdehyde (MDA and protein oxidation product, protein carbonyl. FAC injection in Hlfer-silenced ticks resulted in high mortality. Higher levels of MDA and protein carbonyl were detected in Hlfer-silenced ticks compared to Luciferase-injected (control ticks both after blood feeding and FAC injection. Ferric iron accumulation demonstrated by increased staining on native HlFER was observed from 72 h after iron injection in both the whole tick and the midgut. Furthermore, weak iron staining was observed after Hlfer knockdown. Taken together, these results show that tick ferritins are crucial antioxidant molecules that protect the hard tick from iron-mediated oxidative stress during blood feeding.

  12. Mechanism of Electron Beam Induced Oxide Layer Thickening on Iron–Iron Oxide Core–Shell Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Sundararajan, Jennifer A.; Kaur, Maninder; Qiang, You

    2015-04-16

    Materials exposed to radiation show structural changes and damages, especially in the nanoscale range. The characterizing equipment involving electron beam (e-beam) radiation for a nanosize imaging process, such as a transmission electron microscope, is no exception, in which the most prominent behavior of native oxide layer thickening has been widely studied. In this paper, we describe the physics behind the growth mechanism of the oxide layer in a core–shell iron/iron oxide nanoparticle (NP) under the impact of e-beam radiation. The particles studied were synthesized via a cluster deposition system. Due to the impact of the e-beam, these particles were observed to grow inward and outward resulting in a total increase of NP size. The theory is connected with experimental evidence to reveal the oxide layer thickening of the NP, which is favored and enhanced by vacancy formation, surface oxidation, and diffusion/void nucleation under the impact of a 200 keV e-beam.

  13. In vitro toxicological assessment of iron oxide, aluminium oxide and copper nanoparticles in prokaryotic and eukaryotic cell types.

    Science.gov (United States)

    Sadiq, Rakhshinda; Khan, Qaiser Mahmood; Mobeen, Ameena; Hashmat, Amer Jamal

    2015-04-01

    Metallic nanoparticles (NPs) have a variety of applications in different industries including pharmaceutical industry where these NPs are used mainly for image analysis and drug delivery. The increasing interest in nanotechnology is largely associated with undefined risks to the human health and to the environment. Therefore, in the present study cytotoxic and genotoxic effects of iron oxide, aluminium oxide and copper nanoparticles were evaluated using most commonly used assays i.e. Ames assay, in vitro cytotoxicity assay, micronucleus assay and comet assay. Cytotoxicity to bacterial cells was assessed in terms of colony forming units by using Escherichia coli (gram negative) and Bacillus subtilis (gram positive). Ames assay was carried out using two bacterial strains of Salmonella typhimurium TA98 and TA100. Genotoxicity of these NPs was evaluated following exposure to monkey kidney cell line, CHS-20. No cytotoxic and genotoxic effects were observed for iron oxide, and aluminium oxide NPs. Copper NPs were found mutagenic in TA98 and in TA100 and also found cytotoxic in dose dependent manner. Copper NPs induced significant (p Copper NPs also induced DNA strand breaks at 10 µg/mL and oxidative DNA damage at 5 and 10 µg/mL. We consider these findings very useful in evaluating the genotoxic potential of NPs especially because of their increasing applications in human health and environment with limited knowledge of their toxicity and genotoxicity.

  14. New surface radiolabeling schemes of super paramagnetic iron oxide nanoparticles (SPIONs) for biodistribution studies

    Science.gov (United States)

    Nallathamby, Prakash D.; Mortensen, Ninell P.; Palko, Heather A.; Malfatti, Mike; Smith, Catherine; Sonnett, James; Doktycz, Mitchel J.; Gu, Baohua; Roeder, Ryan K.; Wang, Wei; Retterer, Scott T.

    2015-04-01

    Nanomaterial based drug delivery systems allow for the independent tuning of the surface chemical and physical properties that affect their biodistribution in vivo and the therapeutic payloads that they are intended to deliver. Additionally, the added therapeutic and diagnostic value of their inherent material properties often provides extra functionality. Iron based nanomaterials with their magnetic properties and easily tailorable surface chemistry are of particular interest as model systems. In this study the core radius of the iron oxide nanoparticles (NPs) was 14.08 +/- 3.92 nm while the hydrodynamic radius of the NPs, as determined by Dynamic Light Scattering (DLS), was between 90-110 nm. In this study, different approaches were explored to create radiolabeled NPs that are stable in solution. The NPs were functionalized with polycarboxylate or polyamine surface functional groups. Polycarboxylate functionalized NPs had a zeta potential of -35 mV and polyamine functionalized NPs had a zeta potential of +40 mV. The polycarboxylate functionalized NPs were chosen for in vivo biodistribution studies and hence were radiolabeled with 14C, with a final activity of 0.097 nCi mg-1 of NPs. In chronic studies, the biodistribution profile is tracked using low level radiolabeled proxies of the nanoparticles of interest. Conventionally, these radiolabeled proxies are chemically similar but not chemically identical to the non-radiolabeled NPs of interest. This study is novel as different approaches were explored to create radiolabeled NPs that are stable, possess a hydrodynamic radius of S1) High-Resolution Transmission Electron Microscopy (HRTEM) image of iron oxide nanoparticles, (S2) Superconducting Quantum Interference Device (SQUID) measurement of magnetization of super paramagnetic iron oxide nanoparticles, (S3) Fourier Transform Infrared Spectroscopy (FT-IR) spectra of Fe-Si-COO- synthesised using Grignard reagents (S4) FT-IR spectra of iron oxide nanoparticles

  15. Regional framework and geology of iron oxide-apatite-rare earth element and iron oxide-copper-gold deposits of the Mesoproterozoic St. Francois Mountains Terrane, southeast Missouri

    Science.gov (United States)

    Day, Warren C.; Slack, John F.; Ayuso, Robert A.; Seeger, Cheryl M.

    2016-01-01

    This paper provides an overview on the genesis of Mesoproterozoic igneous rocks and associated iron oxide ± apatite (IOA) ± rare earth element, iron oxide-copper-gold (IOCG), and iron-rich sedimentary deposits in the St. Francois Mountains terrane of southeast Missouri, USA. The St. Francois Mountains terrane lies along the southeastern margin of Laurentia as part of the eastern granite-rhyolite province. The province formed during two major pulses of igneous activity: (1) an older early Mesoproterozoic (ca. 1.50–1.44 Ga) episode of volcanism and granite plutonism, and (2) a younger middle Mesoproterozoic (ca. 1.33–1.30 Ga) episode of bimodal gabbro and granite plutonism. The volcanic rocks are predominantly high-silica rhyolite pyroclastic flows, volcanogenic breccias, and associated volcanogenic sediments with lesser amounts of basaltic to andesitic volcanic and associated subvolcanic intrusive rocks. The iron oxide deposits are all hosted in the early Mesoproterozoic volcanic and volcaniclastic sequences. Previous studies have characterized the St. Francois Mountains terrane as a classic, A-type within-plate granitic terrane. However, our new whole-rock geochemical data indicate that the felsic volcanic rocks are effusive derivatives from multicomponent source types, having compositional similarities to A-type within-plate granites as well as to S- and I-type granites generated in an arc setting. In addition, the volcanic-hosted IOA and IOCG deposits occur within bimodal volcanic sequences, some of which have volcanic arc geochemical affinities, suggesting an extensional tectonic setting during volcanism prior to emplacement of the ore-forming systems.The Missouri iron orebodies are magmatic-related hydrothermal deposits that, when considered in aggregate, display a vertical zonation from high-temperature, magmatic ± hydrothermal IOA deposits emplaced at moderate depths (~1–2 km), to magnetite-dominant IOA veins and IOCG deposits emplaced at shallow

  16. Linkage of iron elution and dissolved oxygen consumption with removal of organic pollutants by nanoscale zero-valent iron: Effects of pH on iron dissolution and formation of iron oxide/hydroxide layer.

    Science.gov (United States)

    Fujioka, Nanae; Suzuki, Moe; Kurosu, Shunji; Kawase, Yoshinori

    2016-02-01

    The iron elution and dissolved oxygen (DO) consumption in organic pollutant removal by nanoscale zero-valent iron (nZVI) was examined in the range of solution pH from 3.0 to 9.0. Their behaviors were linked with the removal of organic pollutant through the dissolution of iron and the formation of iron oxide/hydroxide layer affected strongly by solution pH and DO. As an example of organic pollutants, azo-dye Orange II was chosen in this study. The chemical composition analyses before and after reaction confirmed the corrosion of nZVI into ions, the formation of iron oxide/hydroxide layer on nZVI surface and the adsorption of the pollutant and its intermediates. The complete decolorization of Orange II with nZVI was accomplished very quickly. On the other hand, the total organic carbon (TOC) removal was considerably slow and the maximum TOC removal was around 40% obtained at pH 9.0. The reductive cleavage of azo-bond by emitted electrons more readily took place as compared with the cleavage of aromatic rings of Orange II leading to the degradation to smaller molecules and subsequently the mineralization. A reaction kinetic model based on the Langmuir-Hinshelwood/Eley-Rideal approach was developed to elucidate mechanisms for organic pollutant removal controlled by the formation of iron oxide/hydroxide layer, the progress of which could be characterized by considering the dynamic concentration changes in Fe(2+) and DO. The dynamic profiles of Orange II removal linked with Fe(2+) and DO could be reasonably simulated in the range of pH from 3.0 to 9.0.

  17. Ultrastructural characterization of mesenchymal stromal cells labeled with ultrasmall superparamagnetic iron-oxide nanoparticles for clinical tracking studies

    DEFF Research Database (Denmark)

    Hansen, Louise; Hansen, Alastair B; Mathiasen, Anders B

    2014-01-01

    INTRODUCTION: To evaluate survival and engraftment of mesenchymal stromal cells (MSCs) in vivo, it is necessary to track implanted cells non-invasively with a method, which does not influence cellular ultrastructure and functional characteristics. Iron-oxide particles have been applied for cell...... tracking for years, but knowledge regarding possible cytotoxic ultrastructural changes subsequent to iron-oxide particle labeling is limited. Hence, the purpose of this study was to label MSCs with dextran-coated ultrasmall super-paramagnetic iron-oxide (USPIO) particles conjugated with the transduction...

  18. Precise control over shape and size of iron oxide nanocrystals suitable for assembly into ordered particle arrays

    Science.gov (United States)

    Wetterskog, Erik; Agthe, Michael; Mayence, Arnaud; Grins, Jekabs; Wang, Dong; Rana, Subhasis; Ahniyaz, Anwar; Salazar-Alvarez, German; Bergström, Lennart

    2014-10-01

    Here we demonstrate how monodisperse iron oxide nanocubes and nanospheres with average sizes between 5 and 27 nm can be synthesized by thermal decomposition. The relative importance of the purity of the reactants, the ratio of oleic acid and sodium oleate, the maximum temperature, and the rate of temperature increase, on robust and reproducible size and shape-selective iron oxide nanoparticle synthesis are identified and discussed. The synthesis conditions that generate highly monodisperse iron oxide nanocubes suitable for producing large ordered arrays, or mesocrystals are described in detail.

  19. In Situ Probing Nucleation, Growth, and Aggregation of Iron Oxides in Geochemical Aquatic Systems

    Science.gov (United States)

    Jun, Y.; Hu, Y.; Ray, J. R.

    2012-12-01

    Nucleation, growth, and aggregation of iron oxide nanoparticles can significantly alter the fate of organic and inorganic contaminants in geochemical aquatic systems. This talk will address how we can improve our understanding of nucleation, growth, and aggregation of iron oxide nanoparticles by providing more accurate quantitative and qualitative empirical information. In this study, a novel environmental setup—which allows time-resolved simultaneous measurements of small angle x-ray scattering (SAXS) and grazing incidence small-angle scattering (GISAXS) in the presence of bulk solution—was utilized for real-time monitoring of nanoparticle formation at water-mineral interfaces. This setup enabled us to probe the size, shape, and location of iron oxide nanoparticles on the substrate and in solution without dehydration of samples. Experiments were conducted with 10-4 M ferric ions in the presence of environmentally important and abundant anions (nitrate, chlorite, sulfate) and cations (aluminum) at pH = 3.7 ± 0.1. The substrates used were geologically ubiquitous media such as quartz, mica, and organic polymer-coated surfaces. Once ferric solutions were introduced, the homogeneous and heterogeneous nucleation of iron oxides occurred and the size and volume evolution of nanoparticles were monitored. To complement these observations, atomic force microscopy, high-resolution transmission electron microscopy, high-resolution x-ray diffraction, contact angle analysis, dynamic light scattering, and electrophoretic mobility analysis were utilized. Based on in situ measurements of initial nuclei evolution at aqueous interfaces, this approach provided new, important information for upscaling such as size, volume, surface area, and location (i.e., in solution vs. on mineral surfaces) of iron oxides precipitates formed in the presence of organic matter and different substrate morphological and chemical properties. Using this quantitative information, we identified the

  20. Bacterial and iron oxide aggregates mediate secondary iron mineral formation: green rust versus magnetite.

    Science.gov (United States)

    Zegeye, A; Mustin, C; Jorand, F

    2010-06-01

    In the presence of methanoate as electron donor, Shewanella putrefaciens, a Gram-negative, facultative anaerobe, is able to transform lepidocrocite (gamma-FeOOH) to secondary Fe (II-III) minerals such as carbonated green rust (GR1) and magnetite. When bacterial cells were added to a gamma-FeOOH suspension, aggregates were produced consisting of both bacteria and gamma-FeOOH particles. Recently, we showed that the production of secondary minerals (GR1 vs. magnetite) was dependent on bacterial cell density and not only on iron reduction rates. Thus, gamma-FeOOH and S. putrefaciens aggregation pattern was suggested as the main mechanism driving mineralization. In this study, lepidocrocite bioreduction experiments, in the presence of anthraquinone disulfonate, were conducted by varying the [cell]/[lepidocrocite] ratio in order to determine whether different types of aggregate are formed, which may facilitate precipitation of GR1 as opposed to magnetite. Confocal laser scanning microscopy was used to analyze the relative cell surface area and lepidocrocite concentration within the aggregates and captured images were characterized by statistical methods for spatial data (i.e. variograms). These results suggest that the [cell]/[lepidocrocite] ratio influenced both the aggregate structure and the nature of the secondary iron mineral formed. Subsequently, a [cell]/[lepidocrocite] ratio above 1 x 10(7) cells mmol(-1) leads to densely packed aggregates and to the formation of GR1. Below this ratio, looser aggregates are formed and magnetite was systematically produced. The data presented in this study bring us closer to a more comprehensive understanding of the parameters governing the formation of minerals in dense bacterial suspensions and suggest that screening mineral-bacteria aggregate structure is critical to understanding (bio)mineralization pathways.

  1. Iron-oxide colloidal nanoclusters: from fundamental physical properties to diagnosis and therapy

    Science.gov (United States)

    Kostopoulou, Athanasia; Brintakis, Konstantinos; Lascialfari, Alessandro; Angelakeris, Mavroeidis; Vasilakaki, Marianna; Trohidou, Kalliopi; Douvalis, Alexios P.; Psycharakis, Stylianos; Ranella, Anthi; Manna, Liberato; Lappas, Alexandros

    2014-03-01

    Research on magnetic nanocrystals attracts wide-spread interest because of their challenging fundamental properties, but it is also driven by problems of practical importance to the society, ranging from electronics (e.g. magnetic recording) to biomedicine. In that respect, iron oxides are model functional materials as they adopt a variety of oxidation states and coordinations that facilitate their use. We show that a promising way to engineer further their technological potential in diagnosis and therapy is the assembly of primary nanocrystals into larger colloidal entities, possibly with increased structural complexity. In this context, elevated-temperature nanochemistry (c.f. based on a polyol approach) permitted us to develop size-tunable, low-cytotoxicity iron-oxide nanoclusters, entailing iso-oriented nanocrystals, with enhanced magnetization. Experimental (magnetometry, electron microscopy, Mössbauer and NMR spectroscopies) results supported by Monte Carlo simulations are reviewed to show that such assemblies of surface-functionalized iron oxide nanocrystals have a strong potential for innovation. The clusters' optimized magnetic anisotropy (including microscopic surface spin disorder) and weak ferrimagnetism at room temperature, while they do not undermine colloidal stability, endow them a profound advantage as efficient MRI contrast agents and hyperthermic mediators with important biomedical potential.

  2. Strain induced anomalous red shift in mesoscopic iron oxide prepared by a novel technique

    Indian Academy of Sciences (India)

    T N Narayanan; D Sakthi Kumar; Yasuhiko Yoshida; M R Anantharaman

    2008-10-01

    Nano magnetic oxides are promising candidates for high density magnetic storage and other applications. Nonspherical mesoscopic iron oxide particles are also candidate materials for studying the shape, size and strain induced modifications of various physical properties viz. optical, magnetic and structural. Spherical and nonspherical iron oxides having an aspect ratio, ∼2, are synthesized by employing starch and ethylene glycol and starch and water, respectively by a novel technique. Their optical, structural, thermal and magnetic properties are evaluated. A red shift of 0.24 eV is observed in the case of nonspherical particles when compared to spherical ones. The red shift is attributed to strain induced changes in internal pressure inside the elongated iron oxide particles. Pressure induced effects are due to the increased overlap of wave functions. Magnetic measurements reveal that particles are superparamagnetic. The marked increase in coercivity in the case of elongated particles is a clear evidence for shape induced anisotropy. The decreased specific saturation magnetization of the samples is explained on the basis of weight percentage of starch, a nonmagnetic component and is verified by TGA and FTIR studies. This technique can be modified for tailoring the aspect ratio and these particles are promising candidates for drug delivery and contrast enhancement agents in magnetic resonance imaging.

  3. Evaluation of folate conjugated superparamagnetic iron oxide nanoparticles for scintigraphic/magnetic resonance imaging.

    Science.gov (United States)

    Chauhan, Ram Prakash; Mathur, Rashi; Singh, Gurjaspreet; Kaul, Ankur; Bag, Narmada; Singh, Sweta; Kumar, Hemanth; Patra, Manoj; Mishra, Anil K

    2013-03-01

    The physical and chemical properties of the nanoparticles influence their pharmacokinetics and ability to accumulate in tumors. In this paper we report a facile method to conjugate folic acid molecule to iron oxide nanoparticles to increase the specific uptake of these nanoparticles by the tumor, which will be useful in targeted imaging of the tumor. The iron oxide nanoparticles were synthesized by alkaline co precipitation method and were surface modified with dextranto make them stable. The folic acid is conjugated to the dextran modified iron oxide nanoparticles by reductive amination process after the oxidation of the dextran with periodate. The synthesized folic acid conjugated nanoparticles were characterized for size, phase, morphology and magnetization by using various physicochemical characterization techniques such as transmission electron microscopy, X-ray diffraction, fourier transform infrared spectroscopy, vibrating sample magnetometry, dynamic light scattering and zetasizer etc. The quantification of the generated carbonyl groups and folic acid conjugated to the surface of the magnetic nanoparticles was done by colorimetric estimations using UV-Visible spectroscopy. The in vitro MR studies were carried out over a range of concentrations and showed significant shortening of the transverse relaxation rate, showing the ability of the nanoconjugate to act as an efficient probe for MR imaging. The biodistribution studies and the scintigraphy done by radiolabeling the nanoconjugate with 99mTc show the enhanced uptake at the tumor site showing its enhanced specificity.

  4. Microbial mediated iron redox cycling in Fe (hydr)oxides for nitrite removal.

    Science.gov (United States)

    Lu, Yongsheng; Xu, Lu; Shu, Weikang; Zhou, Jizhi; Chen, Xueping; Xu, Yunfeng; Qian, Guangren

    2017-01-01

    Nitrite, at an environmentally relevant concentration, was significantly reduced with iron (hydr)oxides mediated by Shewanella oneidensis MR-1. The average nitrite removal rates of 1.28±0.08 and 0.65±0.02(mgL(-1))h(-1) were achieved with ferrihydrite and magnetite, respectively. The results showed that nitrite removal was able to undergo multiple redox cycles with iron (hydr)oxides mediated by Shewanella oneidensis MR-1. During the bioreduction of the following cycles, biogenic Fe(II) was subsequently chemically oxidized to Fe(III), which is associated with nitrite reduction. There was 11.18±1.26mgL(-1) of NH4(+)-N generated in the process of redox cycling of ferrihydrite. Additionally, results obtained by using X-ray diffraction showed that ferrihydrite and magnetite remained mainly stable in the system. This study indicated that redox cycling of Fe in iron (hydr)oxides was a potential process associated with NO2(-)-N removal from solution, and reduced most nitrite abiotically to gaseous nitrogen species.

  5. Effect of magnetic field on the zero valent iron induced oxidation reaction

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Dong-hyo; Kim, Jungwon [School of Environmental Science and Engineering, Pohang University of Scienceand Technology (POSTECH), Pohang 790-784 (Korea, Republic of); Choi, Wonyong, E-mail: wchoi@postech.edu [School of Environmental Science and Engineering, Pohang University of Scienceand Technology (POSTECH), Pohang 790-784 (Korea, Republic of)

    2011-08-30

    Highlights: {yields} We investigate the zero valent iron induced oxidation in the presence of magnetic field. {yields} The oxidative degradation of 4-chlorophenol is enhanced by the magnetic field. {yields} ESR measurement confirms that more OH radicals are generated in the presence of magnetic field. {yields} The magnetic field affects the mass transfer of O{sub 2} and the recombination of radicals. - Abstract: The magnetic field (MF) effect on the zero valent iron (ZVI) induced oxidative reaction was investigated for the first time. The degradation of 4-chlorophenol (4-CP) in the ZVI system was employed as the test oxidative reaction. MF markedly enhanced the degradation of 4-CP with the concurrent production of chlorides. The consumption of dissolved O{sub 2} by ZVI reaction was also enhanced in the presence of MF whereas the competing reaction of H{sub 2} production from proton reduction was retarded. Since the ZVI-induced oxidation is mainly driven by the in situ generated hydroxyl radicals, the production of OH radicals was monitored by the spin trap method using electron spin resonance (ESR) spectroscopy. It was confirmed that the concentration of trapped OH radicals was enhanced in the presence of MF. Since both O{sub 2} and Fe{sup 0} are paramagnetic, the diffusion of O{sub 2} onto the iron surface might be accelerated under MF. The magnetized iron can attract oxygen on itself, which makes the mass transfer process faster. As a result, the surface electrochemical reaction between Fe{sup 0} and O{sub 2} can be accelerated with the enhanced production of OH radicals. MF might retard the recombination of OH radicals as well.

  6. Degradation of toluene, ethylbenzene, and xylene using heat and chelated-ferrous iron activated persulfate oxidation

    Science.gov (United States)

    Mondal, P.; Sleep, B.

    2014-12-01

    Toluene, ethylbenze, and xylene (TEX) are common contaminants in the subsurface. Activated persulfate has shown promise for degrading a wide variety of organic compounds. However, studies of persulfate application for in situ degradation of TEX and effects on the subsequent bioremediation are limited. In this work, degradation studies of TEX in aqueous media and soil are being conducted using heat activated and chelated-ferrous iron activated persulfate oxidation in batch and flow-through column experiments. In the batch experiments, sodium persulfate is being used at different concentrations to provide an initial persulfate to TEX molar ratios between 10:1 and 100:1. Sodium persulfate solutions are being activated at 20, 37, 60, and 80 oC temperatures for the heat activated oxidation. For the chelated-ferrous iron activated oxidation, ferrous iron and citric acid, both are being used at concentration of 5 mM. In the experiments with soil slurry, a soil to water ratio of 1 to 5 is being used. Flow through water saturated column experiments are being conducted with glass columns (45 cm in length and 4 cm in diameter) uniformly packed with soils, and equilibrated with water containing TEX at the target concentrations. Both the heat activation and chelated-ferrous iron activation of persulfate are being employed in the column experiments. Future experiments are planned to determine the suitability of persulfate oxidation of TEX on the subsequent biodegradation using batch microcosms containing TEX degrading microbial cultures. In these experiments, the microbial biomass will be monitored using total phospholipids, and the microbial community will be determined using quantitative real-time polymerase chain reaction (qPCR) on the extracted DNA. This study is expected to provide suitable operating conditions for in situ chemical oxidation of TEX with activated persulfate followed by bioremediation.

  7. Preparation and properties of magnetic iron oxide nanotubes

    Institute of Scientific and Technical Information of China (English)

    Baoliang Lv; Yao Xu; Dong Wu; Yuhan Sun

    2008-01-01

    Magnetite (Fe3O4) nanotubes were prepared by reducing synthesized hematite (α-Fe2O3) nanotubes in 5% H2+95% Ar atmosphere,and then maghemite (γ-Fe2O3) nanotubes were obtained by re-oxidizing the Fe3O4 nanotubes.The nanotube structure was kept from collapsing or sintering throughout the high temperature reducing and re-oxidizing processes.The coercivities of the Fe3O4 and γ-Fe2O3 nanotubes synthesized were found to be 340.22 Oe and 342.23 Oe,respectively,both higher than other nanostructures with the same phase and of similar size.Both adsorbed phosphate and the nanotube structure are considered responsible for this high coercivity.

  8. Manganese oxide shuttling in pre-GOE oceans - evidence from molybdenum and iron isotopes

    Science.gov (United States)

    Kurzweil, Florian; Wille, Martin; Gantert, Niklas; Beukes, Nicolas J.; Schoenberg, Ronny

    2016-10-01

    The local occurrence of oxygen-rich shallow marine water environments has been suggested to significantly predate atmospheric oxygenation, which occurred during the Great Oxidation Event (GOE) ca. 2.4 billion years ago. However, the potential influence of such 'oxygen oases' on the mobility, distribution and isotopic composition of redox sensitive elements remains poorly understood. Here, we provide new molybdenum and iron isotopic data from shallow marine carbonate and silicate iron formations of the Koegas Subgroup, South Africa, that confirm local ocean redox stratification prior to the GOE. Mn concentrations correlate negatively with both δ98 Mo and δ56 Fe values, which highlights the substantial role of particulate manganese for the cycling of Mo and Fe in the Paleoproterozoic oceans. Based on these trends we propose that pore water molybdate was recharged (1) by the diffusional transport of seawater molybdate with high δ98 Mo and (2) by the re-liberation of adsorbed molybdate with low δ98 Mo during Mn oxide dissolution within the sediment. The relative contribution of isotopically light Mo is highest close to a Mn chemocline, where the flux of Mn oxides is largest, causing the negative correlation of Mn concentrations and δ98 Mo values in the Koegas sediments. The negative correlation between δ56 Fe values and Mn concentrations is likely related to Fe isotope fractionation during Fe(II) oxidation by Mn oxides, resulting in lower δ56 Fe values in the uppermost water column close to a Mn chemocline. We argue that the preservation of these signals within Paleoproterozoic sediments implies the existence of vertically extended chemoclines with a smoother gradient, probably as a result of low atmospheric oxygen concentrations. Furthermore, we suggest that abiotic oxidation of Fe(II) by a Mn oxide particle shuttle might have promoted the deposition of the Koegas iron formations.

  9. Effects of Iron and Aluminum Oxides and Kaolinite on Adsorpion and Activities on Invertase

    Institute of Scientific and Technical Information of China (English)

    HUANGQIAOYUN; JIANGMINGHUA; 等

    1998-01-01

    Experiments were conducted to study the influences of synthetic bayerite,non-crystalline aluminum oxide(N-AlOH) ,geoethite,non-crystalline iron oxide (N-FeOH) and kaolinite on the adsorption,activity,kinetics and thermal stability of invertase.Adsorption of invertase on iron,aluminum oxides fitted Langmuir equation,The amount of invertase held on the minerals followed the sequence kaolinite>goethite>N-AlOH>bayerite>N-FeOH.No correlation was found between enzyme adsorption and the specific surface area of minerals exmined.The differences in the surface structure of minerals and the arrangement of enzymatic molecules on mineral surfaces led to the different capacities of minerals for enzyme adsorption. The adsorption of invertase on bayerite,N-AlOH,goethite ,H-FeOH and kaolinite was differently affected by pH.The order for the activity of invertase adsorbed on minerals was N-FeOH>N-AlOH>bayerite> goethite> kalinite.The inhibition effect of minerals on enzyme activity was kaolinite> crystalline oxides> non -crystalline oxides.The pH optimum of iron oxide-and aluminum oxide-invertase complexes was sililar to that of free enzyme(pH4.0),whereas the pH optimum of kaolinite-invertase complex was one pH unit highr than that of free enzyme.The affinity to substrate and the maximum reaction velocity as well as the thermal stability of combined inverthase were lower than those of the free enzyme.

  10. Manipulation of pyrite colonization and leaching by iron-oxidizing Acidithiobacillus species.

    Science.gov (United States)

    Bellenberg, Sören; Barthen, Robert; Boretska, Mariia; Zhang, Ruiyong; Sand, Wolfgang; Vera, Mario

    2015-02-01

    In this study, the process of pyrite colonization and leaching by three iron-oxidizing Acidithiobacillus species was investigated by fluorescence microscopy, bacterial attachment, and leaching assays. Within the first 4-5 days, only the biofilm subpopulation was responsible for pyrite dissolution. Pyrite-grown cells, in contrast to iron-grown cells, were able to oxidize iron(II) ions or pyrite after 24 h iron starvation and incubation with 1 mM H₂O₂, indicating that these cells were adapted to the presence of enhanced levels of reactive oxygen species (ROS), which are generated on metal sulfide surfaces. Acidithiobacillus ferrivorans SS3 and Acidithiobacillus ferrooxidans R1 showed enhanced pyrite colonization and biofilm formation compared to A. ferrooxidans (T). A broad range of factors influencing the biofilm formation on pyrite were also identified, some of them were strain-specific. Cultivation at non-optimum growth temperatures or increased ionic strength led to a decreased colonization of pyrite. The presence of iron(III) ions increased pyrite colonization, especially when pyrite-grown cells were used, while the addition of 20 mM copper(II) ions resulted in reduced biofilm formation on pyrite. This observation correlated with a different extracellular polymeric substance (EPS) composition of copper-exposed cells. Interestingly, the addition of 1 mM sodium glucuronate in combination with iron(III) ions led to a 5-fold and 7-fold increased cell attachment after 1 and 8 days of incubation, respectively, in A. ferrooxidans (T). In addition, sodium glucuronate addition enhanced pyrite dissolution by 25%.

  11. Microwave-Assisted Combustion Synthesis of Nano Iron Oxide/Iron-Coated Activated Carbon, Anthracite, Cellulose Fiber, and Silica, with Arsenic Adsorption Studies

    OpenAIRE

    2011-01-01

    Combustion synthesis of iron oxide/iron coated carbons such as activated carbon, anthracite, cellulose fiber, and silica is described. The reactions were carried out in alumina crucibles using a Panasonic kitchen microwave with inverter technology, and the reaction process was completed within a few minutes. The method used no additional fuel and nitrate, which is present in the precursor itself, to drive the reaction. The obtained samples were then characterized with X-ray mapping, scanning...

  12. Iron oxides of Fazendao Deposit, East Border of Quadrilatero FerrIfero, Minas Gerais, Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Pereira, A R P; Fabris, J D [Departamento de Quimica - Universidade Federal de Minas Gerais (Brazil); Rios, F J [Centro de Desenvolvimento da Tecnologia Nuclear - CDTN, Minas Gerais (Brazil); Rosiere, C A, E-mail: arpp@qui.dout.ufmg.b [Instituto de Geociencias - Universidade Federal de Minas Gerais (Brazil)

    2010-03-01

    The iron oxides highly influence the soil structure and aggregation of mineral particles in soil. They also play an important role in some economical variables, as those related to the use of land for agriculture practices or mineral exploitation, in ore mining activities. About 60 % of all industrial activities on iron processing in Brazil is based on ores mined in the geodomain of Quadrilatero FerrIfero, state of Minas Gerais, Brazil. Samples of a mining area for iron, the Fazendao Deposit in the east border of Quadrilatero FerrIfero have been studied in an attempt to contribute to a better understanding of the key chemical and mineralogical pathways related to the formation and transformation of iron oxides, involving hematite. From powder diffraction patterns, it is confirmed that hematite is the main mineralogical phase in all samples. The total iron contents were found to range between 65.15 and 70.00 mass%. The saturation magnetization values, {sigma} = 6.9 and 2.1 J T{sup -1} kg{sup -1} are significantly measurable only for the two samples showing some evidences of magnetite. 298 K-Moessbauer data confirmed the dominant occurrence of hematite in all samples, along with magnetite for the two samples showing non-zero magnetization. 110 K-Moessbauer data indicate that the hematite in all samples undergoes the Morin transition (T{sub M} {approx} 260 K), as expected for the relatively pure oxide. Maghemite could not be detected in any sample. New numerical analysis are now being performed, using Rietveld refinement of XRD data, in an attempt to obtain crystallographic results that could indicate more reliable evidences about the mechanisms of formation of hematite, particularly in the magnetic samples, for which the precursor is presumably magnetite.

  13. Assessment of the role of α-lipoic acid against the oxidative stress of induced iron overload

    Directory of Open Access Journals (Sweden)

    Yasser F. Ali

    2015-01-01

    Full Text Available This work was aimed to study the protective role of α-lipoic acid against the oxidative damage of induced iron overload. Iron (Fe overload is a complication of the treatment, by chronic transfusion, of a number of genetic diseases associated with inadequate red cell production (anemias and of other genetic diseases that lead to excessive iron absorption from the diet. Male rats were injected ip with 5 mg/kg body weight ferrous sulfate for 50 days. The animals were injected ip with α-lipoic acid 20 mg per kg body weight for 21 days. Serum iron, Total Iron Binding Capacity (TIBC, Malonyldialdehyde (MDA, Electron paramagnetic resonance (EPR spectroscopy, UV-visible absorption spectrum of hemoglobin and osmotic fragility were studied. Results showed significant increase in serum iron, total iron binding capacity, and malonyldialdehyde levels in iron-loaded rats. Treatment with lipoic acid (LA resulted in decreasing serum iron and TIBC levels by 47%and 29% respectively. At the same time the lipoic acid decreased the level of the MDA in liver, brain and plasma by 54%, 42% and 74% respectively. Also LA diminished the effect of iron-induced free radicals on erythrocyte membrane integrity; it decreased the elevated average osmotic fragility and decreased the elevated rate of hemolysis. Results from UV-visible spectrophotometric measurement of hemoglobin revealed that no oxidative changes of hemoglobin occurred in iron-loaded rats. EPR spectra showed increased in non-heme ferric ions Fe+3 and free radicals in iron-loaded rats. Whereas the injection of the lipoic acid leads to decreased in such toxic result. In conclusion, these observations suggested that lipoic acid might be a beneficial antioxidant that can be effective for limiting damage from oxidative stress of iron overload.

  14. Oxidative damage to rat brain in iron and copper overloads.

    Science.gov (United States)

    Musacco-Sebio, Rosario; Ferrarotti, Nidia; Saporito-Magriñá, Christian; Semprine, Jimena; Fuda, Julián; Torti, Horacio; Boveris, Alberto; Repetto, Marisa G

    2014-08-01

    This study reports on the acute brain toxicity of Fe and Cu in male Sprague-Dawley rats (200 g) that received 0 to 60 mg kg(-1) (ip) FeCl2 or CuSO4. Brain metal contents and time-responses were determined for rat survival, in situ brain chemiluminescence and phospholipid and protein oxidation products. Metal doses hyperbolically defined brain metal content. Rat survival was 91% and 60% after Fe and Cu overloads. Brain metal content increased from 35 to 114 μg of Fe per g and from 3.6 to 34 μg of Cu per g. Brain chemiluminescence (10 cps cm(-2)) increased 3 and 2 times after Fe and Cu overloads, with half maximal responses (C50) of 38 μg of Fe per g of brain and 15 μg of Cu per g of brain, and with half time responses (t1/2) of 12 h for Fe and 20 h for Cu. Phospholipid peroxidation increased by 56% and 31% with C50 of 40 μg of Fe per g and 20 μg of Cu per g and with t1/2 of 9 h and 14 h. Protein oxidation increased by 45% for Fe with a C50 of 40 μg of Fe per g and 18% for Cu with a C50 of 10 μg of Cu per g and a t1/2 of 12 h for both metals. Fe and Cu brain toxicities are likely mediated by Haber-Weiss type HO˙ formation with subsequent oxidative damage.

  15. Chemical fingerprint of iron oxides related to iron enrichment of banded iron formation from the Cauê Formation - Esperança Deposit, Quadrilátero Ferrífero, Brazil: a laser ablation ICP-MS study

    Directory of Open Access Journals (Sweden)

    Lucilia Aparecida Ramos de Oliveira

    Full Text Available Chemical signatures of iron oxides from dolomitic itabirite and high-grade iron ore from the Esperança deposit, located in the Quadrilátero Ferrífero, indicate that polycyclic processes involving changing of chemical and redox conditions are responsible for the iron enrichment on Cauê Formation from Minas Supergroup. Variations of Mn, Mg and Sr content in different generations of iron oxides from dolomitic itabirite, high-grade iron ore and syn-mineralization quartz-carbonate-hematite veins denote the close relationship between high-grade iron ore formation and carbonate alteration. This indicates that dolomitic itabirite is the main precursor of the iron ore in that deposit. Long-lasting percolation of hydrothermal fluids and shifts in the redox conditions have contributed to changes in the Y/Ho ratio, light/heavy rare earth elements ratio and Ce anomaly with successive iron oxide generations (martite-granular hematite, as well as lower abundance of trace elements including rare earth elements in the younger specularite generations.

  16. Mutations of ferric uptake regulator (fur) impair iron homeostasis, growth, oxidative stress survival, and virulence of Xanthomonas campestris pv. campestris.

    Science.gov (United States)

    Jittawuttipoka, Thichakorn; Sallabhan, Ratiboot; Vattanaviboon, Paiboon; Fuangthong, Mayuree; Mongkolsuk, Skorn

    2010-05-01

    Iron is essential in numerous cellular functions. Intracellular iron homeostasis must be maintained for cell survival and protection against iron's toxic effects. Here, we characterize the roles of Xanthomonas campestris pv. campestris (Xcc) fur, which encodes an iron sensor and a transcriptional regulator that acts in iron homeostasis, oxidative stress, and virulence. Herein, we isolated spontaneous Xcc fur mutants that had high intracellular iron concentrations due to constitutively high siderophore levels and increased expression of iron transport genes. These mutants also had reduced aerobic plating efficiency and resistance to peroxide killing. Moreover, one fur mutant was attenuated on a host plant, thus indicating that fur has important roles in the virulence of X. campestris pv. campestris.

  17. Biological Properties of Iron Oxide Nanoparticles for Cellular and Molecular Magnetic Resonance Imaging

    Directory of Open Access Journals (Sweden)

    Claus-Christian Glüer

    2010-12-01

    Full Text Available Superparamagnetic iron-oxide particles (SPIO are used in different ways as contrast agents for magnetic resonance imaging (MRI: Particles with high nonspecific uptake are required for unspecific labeling of phagocytic cells whereas those that target specific molecules need to have very low unspecific cellular uptake. We compared iron-oxide particles with different core materials (magnetite, maghemite, different coatings (none, dextran, carboxydextran, polystyrene and different hydrodynamic diameters (20–850 nm for internalization kinetics, release of internalized particles, toxicity, localization of particles and ability to generate contrast in MRI. Particle uptake was investigated with U118 glioma cells und human umbilical vein endothelial cells (HUVEC, which exhibit different phagocytic properties. In both cell types, the contrast agents Resovist, B102, non-coated Fe3O4 particles and microspheres were better internalized than dextran-coated Nanomag particles. SPIO uptake into the cells increased with particle/iron concentrations. Maximum intracellular accumulation of iron particles was observed between 24 h to 36 h of exposure. Most particles were retained in the cells for at least two weeks, were deeply internalized, and only few remained adsorbed at the cell surface. Internalized particles clustered in the cytosol of the cells. Furthermore, all particles showed a low toxicity. By MRI, monolayers consisting of 5000 Resovist-labeled cells could easily be visualized. Thus, for unspecific cell labeling, Resovist and microspheres show the highest potential, whereas Nanomag particles are promising contrast agents for target-specific labeling.

  18. Briquetting of self-reducing blendings of waste iron oxides mixture

    Energy Technology Data Exchange (ETDEWEB)

    Derungs, P.; Brouhon, J.M.; Harp, G. [ProfilARBED, Esch-sur-Alzette (Luxembourg)

    2002-07-01

    Protection of the environment increasingly requires the reuse of by-products from the steel industry. The objectives of the project were to develop technologies to manufacture self-reducing briquettes out of waste iron oxides and to recycle them in an electric arc furnace or a cupola furnace. CRM has investigated and determinated the optimal characteristics (binder, size, grain size, compositions and activator for the reduction reaction) for briquettes containing mixtures of mill scales, mill sludges, electric arc furnace (EAF) dust and coal as reduction agent. The goal to obtain briquettes, in which iron oxides are totally reduced when these briquettes are loaded with the scrap into an electric are furnace, was achieved. Trials at ProfilARBED have shown that it is possible to recycle mill and EAF by-products conditioned in self-reducing briquettes in an electric arc furnace without influence on the performance and on the environment. The iron content of the slag does not increase as the iron of the by-products is almost completely reduced. Zinc is completely removed and the concentration in the EAF dust increases. BFI has investigated the best recycling method for sludge and dust of the blast furnace (BF) and basic oxygen furnace (BOF), by laboratory testing and industrial trials in a cupola furnace. Self-reducing briquettes have been produced and reduced. The best conditions to achieve the required briquetting strength have been determinated. 29 refs., 74 figs., 38 tabs.

  19. Briquetting of self-reducing blendings of waste iron oxide mixtures. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Derungs, P.; Brouhon, J.M.; Harp, G. [ProfilARBED, Esch-sur Alzette (Luxembourg)

    2002-07-01

    The objectives of this project were to develop technologies to manufacture self-reducing briquettes out of waste iron oxides and to recycle them in an electric arc furnace or a cupola furnace. CRM has investigated and determined the optimal characteristics (binder, size, grain size, compositions and activator for the reduction reaction) for briquettes containing mixtures of mill scales, mill sludges, electric arc furnace (EAF) dust and coal as reduction agent. The goal of obtaining briquettes, in which iron oxides are totally reduced when these briquettes are loaded with the scrap into an electric arc furnace, was achieved. Trials at ProfilARBED have shown that it is possible to recycle mill and EAF by-products conditioned in self-reducing briquettes in an electric arc furnace without influence on the performance and on the environment. The iron content of the slag does not increase as the iron of the by-product is almost completely reduced. Zinc is completely removed and the concentration in the EAF dust increases. BFI has investigated the best recycling method for sludge and dust of the blast furnace and basic oxygen furnace, by laboratory testing and industrial trials in a cupola furnace. Self-reducing briquettes have been produced and reduced. The best conditions for achieving the required briquetting have been determined.

  20. A photonic crystal biosensor assay for ferritin utilizing iron-oxide nanoparticles.

    Science.gov (United States)

    Peterson, Ross D; Cunningham, Brian T; Andrade, Juan E

    2014-06-15

    Iron deficiency anemia afflicts 1 in 3 individuals, mostly women and children worldwide. A novel application using iron-oxide nanoparticles (IONPs) and a photonic crystal (PC) optical biosensor as an immunodiagnostic platform for detection of serum ferritin, a biomarker for iron deficiency, is presented. Human liver ferritin (450 kDa), clinical serum controls, and three commercially available ferritin ELISA tests were used to evaluate the PC biosensor assay in terms of inter- and intra-assay variability, spike-recovery (%), limit of detection (LOD), and matrix effects on binding. For the PC biosensor, signal response from label-free, sandwich with secondary antibody (pAb), and pAb functionalized with iron-oxide nanoparticles (FpAb) assays were detected using the Biomolecular Interaction Detection (BIND) system. Bland-Altman analysis was used to evaluate agreement between expected values for ferritin in control sera and each of the detection platforms. Inter- and intra-assay variability of the PC biosensor were both detection sensitivity of PC biosensors for determination of biomarkers of nutritional status.

  1. Effects of iron and aluminum oxides and clay content on penetration resistance of five Greek soils

    Directory of Open Access Journals (Sweden)

    Stefanos Stefanou

    2013-07-01

    Full Text Available The effect of amorphous and crystalline iron (Fe and aluminum (Al oxides and oxy-hydroxides as well as clay on soil penetration resistance of five Greek soils, as a function of soil water suction was studied for the whole range of soil moisture. The soils tested were of loamy texture and were collected from cultivated and non-cultivated areas of north and central Greece (Macedonia and Thessaly. The study aimed at understanding the role of the above mentioned soil components on penetration resistance. The findings showed that the increase of iron and aluminum oxides and oxy-hydroxides content resulted in an increase of soil penetration resistance and the relationships between them were significant. Crystalline iron forms found to have a more profound effect on penetration resistance as compared to amorphous iron forms. Finally, positive and significant relationships were also found between penetration resistance and clay content. However, it is not entirely clear which of the two soil components plays the most important role in penetration resistance changes in soils.

  2. Ferritins control interaction between iron homeostasis and oxidative stress in Arabidopsis.

    Science.gov (United States)

    Ravet, Karl; Touraine, Brigitte; Boucherez, Jossia; Briat, Jean-François; Gaymard, Frédéric; Cellier, Françoise

    2009-02-01

    Ferritin protein nanocages are the main iron store in mammals. They have been predicted to fulfil the same function in plants but direct evidence was lacking. To address this, a loss-of-function approach was developed in Arabidopsis. We present evidence that ferritins do not constitute the major iron pool either in seeds for seedling development or in leaves for proper functioning of the photosynthetic apparatus. Loss of ferritins in vegetative and reproductive organs resulted in sensitivity to excess iron, as shown by reduced growth and strong defects in flower development. Furthermore, the absence of ferritin led to a strong deregulation of expression of several metal transporters genes in the stalk, over-accumulation of iron in reproductive organs, and a decrease in fertility. Finally, we show that, in the absence of ferritin, plants have higher levels of reactive oxygen species, and increased activity of enzymes involved in their detoxification. Seed germination also showed higher sensitivity to pro-oxidant treatments. Arabidopsis ferritins are therefore essential to protect cells against oxidative damage.

  3. Iron, oxidative stress, and virulence: roles of iron-sensitive transcription factor Sre1 and the redox sensor ChAp1 in the maize pathogen Cochliobolus heterostrophus.

    Science.gov (United States)

    Zhang, Ning; MohdZainudin, Nur A I; Scher, Keren; Condon, Bradford J; Horwitz, Benjamin A; Turgeon, B Gillian

    2013-12-01

    The gene SRE1, encoding the GATA transcription factor siderophore biosynthesis repressor (Sre1), was identified in the genome of the maize pathogen Cochliobolus heterostrophus and deleted. Mutants were altered in sensitivity to iron, oxidative stress, and virulence to the host. To gain insight into mechanisms of this combined regulation, genetic interactions among SRE1 (the nonribosomal peptide synthetase encoding gene NPS6, which is responsible for extracellular siderophore biosynthesis) and ChAP1 (encoding a transcription factor regulating redox homeostasis) were studied. To identify members of the Sre1 regulon, expression of candidate iron and oxidative stress-related genes was assessed in wild-type (WT) and sre1 mutants using quantitative reverse-transcription polymerase chain reaction. In sre1 mutants, NPS6 and NPS2 genes, responsible for siderophore biosynthesis, were derepressed under iron replete conditions, whereas the high-affinity reductive iron uptake pathway associated gene, FTR1, was not, in contrast to outcomes with other well-studied fungal models. C. heterostrophus L-ornithine-N(5)- monooxygenase (SIDA2), ATP-binding cassette (ABC6), catalase (CAT1), and superoxide dismutase (SOD1) genes were also derepressed under iron-replete conditions in sre1 mutants. Chap1nps6 double mutants were more sensitive to oxidative stress than either Chap1 or nps6 single mutants, while Chap1sre1 double mutants showed a modest increase in resistance compared with single Chap1 mutants but were much more sensitive than sre1 mutants. These findings suggest that the NPS6 siderophore indirectly contributes to redox homeostasis via iron sequestration, while Sre1 misregulation may render cells more sensitive to oxidative stress. The double-mutant phenotypes are consistent with a model in which iron sequestration by NPS6 defends the pathogen against oxidative stress. C. heterostrophus sre1, nps6, Chap1, Chap1nps6, and Chap1sre1 mutants are all reduced in virulence toward the

  4. Mapping iron oxides with Landsat-8/OLI and EO-1/Hyperion imagery from the Serra Norte iron deposits in the Carajás Mineral Province, Brazil

    Directory of Open Access Journals (Sweden)

    Diego Fernando Ducart

    Full Text Available ABSTRACT: Mapping methods for iron oxides and clay minerals, using Landsat-8/Operational Land Imager (OLI and Earth Observing 1 (EO-1/Hyperion imagery integrated with airborne geophysical data, were applied in the N4, N5, and N4WS iron deposits, Serra Norte, Carajás, Brazil. Band ratios were achieved on Landsat-8/OLI imagery, allowing the recognition of the main minerals from iron deposits. The Landsat-8/OLI imagery showed a robust performance for iron oxide exploration, even in vegetated shrub areas. Feature extraction and Spectral Angle Mapper hyperspectral classification methods were carried out on EO-1/Hyperion imagery with good results for mapping high-grade iron ore, the hematite-goethite ratio, and clay minerals from regolith. The EO-1/Hyperion imagery proved an excellent tool for fast remote mineral mapping in open-pit areas, as well as mapping waste and tailing disposal facilities. An unsupervised classification was carried out on a data set consisting of EO-1/Hyperion visible near-infrared 74 bands, Landsat-8/OLI-derived Normalized Difference Vegetation Index, Laser Imaging Detection and Ranging-derived Digital Terrain Model, and high-resolution airborne geophysical data (gamma ray spectrometry, Tzz component of gradiometric gravimetry data. This multisource classification proved to be an adequate alternative for mapping iron oxides in vegetated shrub areas and to enhance the geology of the regolith and mineralized areas.

  5. Sol-gel synthesis and characterization of mesoporous iron-titanium mixed oxide for catalytic application

    Energy Technology Data Exchange (ETDEWEB)

    Parida, K.M., E-mail: paridakulamani@yahoo.com [Colloids and Materials Chemistry Department, Institute of Minerals and Materials Technology, Bhubaneswar 751013, Orissa (India); Pradhan, Gajendra Kumar [Colloids and Materials Chemistry Department, Institute of Minerals and Materials Technology, Bhubaneswar 751013, Orissa (India)

    2010-10-01

    A mixed phase of mesoporous iron-titanium mixed oxide (ITMO) has been successfully synthesized by simple sol-gel technique by taking iron (II) sulphate and Ti-isopropoxide as the precursors and sodium dodecyl sulphate (SDS) as the surfactant. The prepared catalysts were characterized by X-ray diffraction (XRD), fourier transform infrared spectroscopy (FTIR), diffuse reflectance UV-vis spectra (UV-vis DRS), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), atomic absorption spectroscopy (AAS), N{sub 2} adsorption-desorptions isotherm, temperature programmed desorption (TPD) and gas chromatography (GC). Low-angle XRD (LAXRD) as well as surface area analysis confirms the mesoporosity nature of the catalysts. The phase and crystallinity were revealed by XRD study. The crystallinity of the catalysts increased with increase in calcinations temperature. Catalysts screening were performed for oxidation of cyclohexane to cyclohexanol and cyclohexanone.

  6. LHRH-functionalized superparamagnetic iron oxide nanoparticles for breast cancer targeting and contrast enhancement in MRI

    Energy Technology Data Exchange (ETDEWEB)

    Meng, J.; Fan, J. [Princeton Institute of Science and Technology of Materials and the Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ 08544 (United States); Galiana, G. [Department of Chemistry, Princeton University, Princeton, NJ 08544 (United States); Branca, R.T. [Department of Chemistry, Duke University, Durham, NC 27708-0354 (United States); Clasen, P.L.; Ma, S. [Center for Advanced Materials and Nanotechnology, Lehigh University, Bethlehem, PA 18015-3195 (United States); Zhou, J. [Princeton Institute of Science and Technology of Materials and the Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ 08544 (United States); Leuschner, C. [Pennington Biomedical Research Center, 6400 Perkins Road, Baton Rouge, LA 70808 (United States); Kumar, C.S.S.R.; Hormes, J. [Center for Advanced Microstructures and Devices, Louisiana State University, 6980 Jefferson Hwy, Baton Rouge, LA 70806 (United States); Otiti, T. [Department of Physics, Makerere University, Kampala (Uganda); Beye, A.C. [Department of Physics, Cheikh Anta Diop University, Dakar (Senegal); Harmer, M.P.; Kiely, C.J. [Center for Advanced Materials and Nanotechnology, Lehigh University, Bethlehem, PA 18015-3195 (United States); Warren, W. [Department of Chemistry, Duke University, Durham, NC 27708-0354 (United States); Haataja, M.P. [Princeton Institute of Science and Technology of Materials and the Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ 08544 (United States); Soboyejo, W.O., E-mail: soboyejo@princeton.edu [Princeton Institute of Science and Technology of Materials and the Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ 08544 (United States)

    2009-05-05

    This paper shows that superparamagnetic iron oxide nanoparticles (SPIONs) conjugated to luteinizing hormone releasing hormone (LHRH) (LHRH-SPIONs), can be used to target breast cancer cells. They also act as contrast enhancement agents during the magnetic resonance imaging of breast cancer xenografts. A combination of transmission electron microscopy (TEM) and spectrophotometric analysis was used in our experiments, to investigate the specific accumulation of the functionalized superparamagnetic iron oxide nanoparticles (SPIONs) in cancer cells. The contrast enhancement of conventional T2 images obtained from the tumor tissue and of breast cancer xenograft bearing mice is shown to be much greater than that in saline controls, when the tissues were injected with LHRH-SPIONs. Magnetic anisotropy multi-CRAZED images of tissues extracted from mice injected with SPIONs were also found to have enhanced MRI contrast in breast cancer xenografts and metastases in the lungs.

  7. Integrated Chemical Systems: The Simultaneous Formation of Hybrid Nanocomposites of Iron Oxide and Organo Silsesquioxanes

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, L; Clapsaddle, B; Jr., J S; Schaefer, D; Shea, K

    2004-10-15

    A sol-gel approach for the synthesis of hybrid nanocomposites of iron oxide and bridged polysilsesquioxanes has been established. The procedures allow for the simultaneous formation of iron oxide and polysilsesquioxane networks in monolithic xerogels and aerogels. These hybrid nanocomposites are synthesized from FeCl{sub 3} {center_dot} 6H{sub 2}O and functionalized silsesquioxane monomers in a one-pot reaction using epoxides as a gelation agent. The porosity and microstructure of the materials has been determined by nitrogen porosimetry, electron microscopy and ultra small angle X-ray scattering (USAXS). The hybrid nanocomposites exhibit a uniform dispersion of both components with no evidence for phase separation at length scales > 5 nm. At this limit of resolution it is not possible to distinguish between two independent interpenetrating networks integrated at molecular length scales or a random copolymer or mixtures of both.

  8. Large-Scale Synthesis of Single-Crystalline Iron Oxide Magnetic Nanorings

    DEFF Research Database (Denmark)

    Jia, Chun-Jiang; Sun, Ling-Dong; Luo, Feng

    2008-01-01

    We present an innovative approach to the production of single-crystal iron oxide nanorings employing a solution-based route. Single-crystal hematite (alpha-Fe2O3) nanorings were synthesized using a double anion-assisted hydrothermal method (involving phosphate and sulfate ions), which can...... be divided into two stages: (1) formation of capsule-shaped alpha-Fe2O3 nanoparticles and (2) preferential dissolution along the long dimension of the elongated nanoparticles (the c axis of alpha-Fe2O3) to form nanorings. The shape of the nanorings is mainly regulated by the adsorption of phosphate ions...... an intriguing three-dimensional magnetic configuration. This work provides an easily scaled-up method for preparing tailor-made iron oxide nanorings that could meet the demands of a variety of applications ranging from medicine to magnetoelectronics....

  9. Magnetic Iron Oxide Nanoparticles for Multimodal Imaging and Therapy of Cancer

    Directory of Open Access Journals (Sweden)

    In-Kyu Park

    2013-07-01

    Full Text Available Superparamagnetic iron oxide nanoparticles (SPION have emerged as an MRI contrast agent for tumor imaging due to their efficacy and safety. Their utility has been proven in clinical applications with a series of marketed SPION-based contrast agents. Extensive research has been performed to study various strategies that could improve SPION by tailoring the surface chemistry and by applying additional therapeutic functionality. Research into the dual-modal contrast uses of SPION has developed because these applications can save time and effort by reducing the number of imaging sessions. In addition to multimodal strategies, efforts have been made to develop multifunctional nanoparticles that carry both diagnostic and therapeutic cargos specifically for cancer. This review provides an overview of recent advances in multimodality imaging agents and focuses on iron oxide based nanoparticles and their theranostic applications for cancer. Furthermore, we discuss the physiochemical properties and compare different synthesis methods of SPION for the development of multimodal contrast agents.

  10. Iron oxide nanoparticles stabilized with a bilayer of oleic acid for magnetic hyperthermia and MRI applications

    Science.gov (United States)

    Soares, Paula I. P.; Laia, César A. T.; Carvalho, Alexandra; Pereira, Laura C. J.; Coutinho, Joana T.; Ferreira, Isabel M. M.; Novo, Carlos M. M.; Borges, João Paulo

    2016-10-01

    Iron oxide nanoparticles (Fe3O4, IONPs) are promising candidates for several biomedical applications such as magnetic hyperthermia and as contrast agents for magnetic resonance imaging (MRI). However, their colloidal stability in physiological conditions hinders their application requiring the use of biocompatible surfactant agents. The present investigation focuses on obtaining highly stable IONPs, stabilized by the presence of an oleic acid bilayer. Critical aspects such as oleic acid concentration and pH were optimized to ensure maximum stability. NPs composed of an iron oxide core with an average diameter of 9 nm measured using transmission electron microscopy (TEM) form agglomerates with an hydrodynamic diameter of around 170 nm when dispersed in water in the presence of an oleic acid bilayer, remaining stable (zeta potential of -120 mV). Magnetic hyperthermia and the relaxivities measurements show high efficiency at neutral pH which enables their use for both magnetic hyperthermia and MRI.

  11. T1-MRI Fluorescent Iron Oxide Nanoparticles by Microwave Assisted Synthesis

    Science.gov (United States)

    Bhavesh, Riju; Lechuga-Vieco, Ana V.; Ruiz-Cabello, Jesús; Herranz, Fernando

    2015-01-01

    Iron oxide nanoparticles have long been studied as a T2 contrast agent in MRI due to their superparamagnetic behavior. T1-based positive contrast, being much more favorable for clinical application due to brighter and more accurate signaling is, however, still limited to gadolinium- or manganese-based imaging tools. Though being the only available commercial positive-contrast agents, they lack an efficient argument when it comes to biological toxicity and their circulatory half-life in blood. The need arises to design a biocompatible contrast agent with a scope for easy surface functionalization for long circulation in blood and/or targeted imaging. We hereby propose an extremely fast microwave synthesis for fluorescein-labeled extremely-small iron oxide nanoparticles (fdIONP), in a single step, as a viable tool for cell labeling and T1-MRI. We demonstrate the capabilities of such an approach through high-quality magnetic resonance angiographic images of mice.

  12. T1-MRI Fluorescent Iron Oxide Nanoparticles by Microwave Assisted Synthesis

    Directory of Open Access Journals (Sweden)

    Riju Bhavesh

    2015-11-01

    Full Text Available Iron oxide nanoparticles have long been studied as a T2 contrast agent in MRI due to their superparamagnetic behavior. T1-based positive contrast, being much more favorable for clinical application due to brighter and more accurate signaling is, however, still limited to gadolinium- or manganese-based imaging tools. Though being the only available commercial positive-contrast agents, they lack an efficient argument when it comes to biological toxicity and their circulatory half-life in blood. The need arises to design a biocompatible contrast agent with a scope for easy surface functionalization for long circulation in blood and/or targeted imaging. We hereby propose an extremely fast microwave synthesis for fluorescein-labeled extremely-small iron oxide nanoparticles (fdIONP, in a single step, as a viable tool for cell labeling and T1-MRI. We demonstrate the capabilities of such an approach through high-quality magnetic resonance angiographic images of mice.

  13. A novel nanostructured iron oxide-gold bioelectrode for hydrogen peroxide sensing

    Science.gov (United States)

    Thandavan, Kavitha; Gandhi, Sakthivel; Sethuraman, Swaminathan; Bosco Balaguru Rayappan, John; Maheswari Krishnan, Uma

    2011-07-01

    Fe3O4 nanoparticles covalently linked to a gold electrode have been used for immobilizing catalase (CAT) enzyme to sense the presence of various concentrations of H2O2. These nanoparticles ranging from 20 to 30 nm were synthesized by thermal co-precipitation of ferric and ferrous chlorides. SEM and XRD have been used for morphological and structural characterization of Fe3O4 nanoparticles. CAT enzyme was linked covalently to the surface of iron oxide using carbodiimide in phosphate buffer (pH 7.4) at 4 °C. The enzyme-iron oxide link was confirmed by FT-IR spectroscopy. Sensing studies carried out using cyclic voltammetry showed a linear response of the CAT/nano Fe3O4/Au bioelectrode towards H2O2 between 1.5 and 13.5 µM with a very sharp response time of 2 s.

  14. High-performance iron oxide nanoparticles for magnetic particle imaging - guided hyperthermia (hMPI)

    Science.gov (United States)

    Bauer, Lisa M.; Situ, Shu F.; Griswold, Mark A.; Samia, Anna Cristina S.

    2016-06-01

    Magnetic particle imaging (MPI) is an emerging imaging modality that allows the direct and quantitative mapping of iron oxide nanoparticles. In MPI, the development of tailored iron oxide nanoparticle tracers is paramount to achieving high sensitivity and good spatial resolution. To date, most MPI tracers being developed for potential clinical applications are based on spherical undoped magnetite nanoparticles. For the first time, we report on the systematic investigation of the effects of changes in chemical composition and shape anisotropy on the MPI performance of iron oxide nanoparticle tracers. We observed a 2-fold enhancement in MPI signal through selective doping of magnetite nanoparticles with zinc. Moreover, we demonstrated focused magnetic hyperthermia heating by adapting the field gradient used in MPI. By saturating the iron oxide nanoparticles outside of a field free region (FFR) with an external static field, we can selectively heat a target region in our test sample. By comparing zinc-doped magnetite cubic nanoparticles with undoped spherical nanoparticles, we could show a 5-fold improvement in the specific absorption rate (SAR) in magnetic hyperthermia while providing good MPI signal, thereby demonstrating the potential for high-performance focused hyperthermia therapy through an MPI-guided approach (hMPI).Magnetic particle imaging (MPI) is an emerging imaging modality that allows the direct and quantitative mapping of iron oxide nanoparticles. In MPI, the development of tailored iron oxide nanoparticle tracers is paramount to achieving high sensitivity and good spatial resolution. To date, most MPI tracers being developed for potential clinical applications are based on spherical undoped magnetite nanoparticles. For the first time, we report on the systematic investigation of the effects of changes in chemical composition and shape anisotropy on the MPI performance of iron oxide nanoparticle tracers. We observed a 2-fold enhancement in MPI signal

  15. Cellular uptake of folate-conjugated lipophilic superparamagnetic iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Woo, Kyoungja [Nano-Materials Research Center, Korea Institute of Science and Technology, P. O. Box 131, Cheongryang, Seoul 130-650 (Korea, Republic of)], E-mail: kjwoo@kist.re.kr; Moon, Jihyung [Nano-Materials Research Center, Korea Institute of Science and Technology, P. O. Box 131, Cheongryang, Seoul 130-650 (Korea, Republic of); Department of Materials Science and Engineering, Korea University, 5-1, Anam-Dong, Sungbook-Ku, Seoul, 136-713 (Korea, Republic of); Choi, Kyu-Sil [Division of Molecular Imaging, Samsung Biomedical Research Institute, Samsung Medical Center, 50 Ilwon-Dong, Kangnam-Ku, Seoul 135-710 (Korea, Republic of); Seong, Tae-Yeon [Department of Materials Science and Engineering, Korea University, 5-1, Anam-Dong, Sungbook-Ku, Seoul, 136-713 (Korea, Republic of); Yoon, Kwon-Ha [Institute for Radiological Imaging Science, Wonkwang University School of Medicine, 344-2, Shinyong, Iksan, Jeonbuk 570-749 (Korea, Republic of)

    2009-05-15

    We prepared five folate-conjugated lipophilic superparamagnetic iron oxide nanoparticles (F{sub 5}-Liposuperparamagnetic iron oxide nanoparticles(SPIONs), 5.5 and 11 nm) and investigated their cellular uptake with KB cells, which is one of the representative folate-receptor over-expressing human epidermoid carcinoma cells, using MRI. The cellular uptake tests with the respective 5.5 and 11 nm F{sub 5}-LipoSPIONs at a fixed particle concentration showed appreciable amount of receptor-mediated uptakes and the specificity was higher in 5.5 nm SPIONs, due to its higher folic acid (FA) density, without inhibition. However, the numbers of the particles taken up under FA inhibition were similar, irrespective of their sizes.

  16. Investigation of structure and magnetic properties of nanocrystalline iron oxide powders for use in magnetic fluids

    Energy Technology Data Exchange (ETDEWEB)

    Lukashova, N.V.; Savchenko, A.G. [National University of Science and Technology ’’MISIS’’, 4, Leninsky pr., Moscow (Russian Federation); Yagodkin, Yu.D., E-mail: yag52@mail.ru [National University of Science and Technology ’’MISIS’’, 4, Leninsky pr., Moscow (Russian Federation); Muradova, A.G.; Yurtov, E.V. [Mendeleev University of Chemical Technology, Miusskaya sq., 9, Moscow (Russian Federation)

    2014-02-15

    Highlights: • The iron oxide nanopowders were obtained by chemical methods. • The particles of the nanopowders had different size. • The structure and magnetic behavior of the powders depend on nanoparticle size. -- Abstract: Iron oxide nanopowders with particles of different size, obtained by co-precipitation and sonochemical methods, were studied by X-ray diffraction, transmission electron microscopy and Mössbauer spectroscopy. The average size of nanoparticles obtained by a co-precipitation method, was about 10 nm. The main phase component of such nanoparticles was maghemite phase γ-Fe{sub 2}O{sub 3}. It was shown, that these nanoparticles were superparamagnetic. In contrast, the nanoparticles obtained by sonochemical method, consisted of larger particles with an average size of around 25 nm. Their main phase component was magnetite Fe{sub 3}O{sub 4}. This powder clearly showed hard magnetic properties.

  17. Surface functionalization of dopamine coated iron oxide nanoparticles for various surface functionalities

    Science.gov (United States)

    Sherwood, Jennifer; Xu, Yaolin; Lovas, Kira; Qin, Ying; Bao, Yuping

    2017-04-01

    We present effective conjugation of four small molecules (glutathione, cysteine, lysine, and Tris(hydroxymethyl)aminomethane) onto dopamine-coated iron oxide nanoparticles. Conjugation of these molecules could improve the surface functionality of nanoparticles for more neutral surface charge at physiological pH and potentially reduce non-specific adsorption of proteins to nanoparticles surfaces. The success of conjugation was evaluated with dynamic light scattering by measuring the surface charge changes and Fourier transform infrared spectroscopy for surface chemistry analysis. The stability of dopamine-coated nanoparticles and the ability of conjugated nanoparticles to reduce the formation of protein corona were evaluated by measuring the size and charge of the nanoparticles in biological medium. This facile conjugation method opens up possibilities for attaching various surface functionalities onto iron oxide nanoparticle surfaces for biomedical applications.

  18. Fluorophore-conjugated iron oxide nanoparticle labeling and analysis of engrafting human hematopoietic stem cells

    DEFF Research Database (Denmark)

    Maxwell, Dustin J; Bonde, Jesper; Hess, David A

    2008-01-01

    The use of nanometer-sized iron oxide particles combined with molecular imaging techniques enables dynamic studies of homing and trafficking of human hematopoietic stem cells (HSC). Identifying clinically applicable strategies for loading nanoparticles into primitive HSC requires strictly defined...... culture conditions to maintain viability without inducing terminal differentiation. In the current study, fluorescent molecules were covalently linked to dextran-coated iron oxide nanoparticles (Feridex) to characterize human HSC labeling to monitor the engraftment process. Conjugating fluorophores...... or in vivo. Transplantation of purified primary human cord blood lineage-depleted and CD34(+) cells into immunodeficient mice allowed detection of labeled human HSC in the recipient bones. Flow cytometry was used to precisely quantitate the cell populations that had sequestered the nanoparticles...

  19. Determination of anisotropy constants of protein encapsulated iron oxide nanoparticles by electron magnetic resonance

    Energy Technology Data Exchange (ETDEWEB)

    Li Hongyan [Department of Physics, Montana State University, Bozeman, MT 59717 (United States); Center for Bio-Inspired Nanomaterials, Montana State University, Bozeman, MT 59717 (United States); Klem, Michael T.; Sebby, Karl B.; Singel, David J. [Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT 59717 (United States); Center for Bio-Inspired Nanomaterials, Montana State University, Bozeman, MT 59717 (United States); Young, Mark [Department of Plant Sciences and Plant Pathology, Montana State University, Bozeman, MT 59717 (United States); Center for Bio-Inspired Nanomaterials, Montana State University, Bozeman, MT 59717 (United States); Douglas, Trevor [Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT 59717 (United States); Center for Bio-Inspired Nanomaterials, Montana State University, Bozeman, MT 59717 (United States); Idzerda, Yves U. [Department of Physics, Montana State University, Bozeman, MT 59717 (United States); Center for Bio-Inspired Nanomaterials, Montana State University, Bozeman, MT 59717 (United States)], E-mail: Idzerda@montana.edu

    2009-02-15

    Angle-dependent electron magnetic resonance was performed on 4.9, 8.0, and 19 nm iron oxide nanoparticles encapsulated within protein capsids and suspended in water. Measurements were taken at liquid nitrogen temperature after cooling in a 1 T field to partially align the particles. The angle dependence of the shifts in the resonance field for the iron oxide nanoparticles (synthesized within Listeria-Dps, horse spleen ferritin, and cowpea chlorotic mottle virus) all show evidence of a uniaxial anisotropy. Using a Boltzmann distribution for the particles' easy-axis direction, we are able to use the resonance field shifts to extract a value for the anisotropy energy, showing that the anisotropy energy density increases with decreasing particle size. This suggests that surface anisotropy plays a significant role in magnetic nanoparticles of this size.

  20. Influence of magnesium on biochemical parameters of iron and oxidative stress in patients with type 2 diabetes

    Directory of Open Access Journals (Sweden)

    Fabiane Araùjo Sampaio

    Full Text Available Introduction: Studies have shown that oxidative stress, found in patients with type 2 diabetes, may be due to changes in the metabolism of minerals, such as magnesium and iron. Data related to compartmentalization of these minerals in diabetes are scarce and controversial. Objective: This study assessed the influence of magnesium on biochemical parameters of iron and oxidative stress in patients with type 2 diabetes. Methods: A case-control study in male and female subjects aged 27-59 years, divided into two groups: type 2 diabetes (n=40 and control (n=48. Intake of magnesium and iron was assessed by three-day food record. Plasma, erythrocyte and urinary levels of magnesium, serum iron, ferritin, total iron binding capacity, fasting glucose, glycated hemoglobin, insulin, creatinine clearance and plasma thiobarbituric acid reactive substances (TBARS were analyzed. Results and Discussion: Magnesium intake and plasma magnesium were lower in diabetic subjects. There was low urinary magnesium excretion, with no difference between groups. Although normal, the diabetic group had lower serum iron and ferritin concentrations compared to control subjects. Plasma TBARS in diabetic patients was higher than control while creatinine clearance was lower. An inverse correlation between erythrocyte magnesium and serum iron and ferritin was observed in the diabetes group. Conclusions: Diabetes induced hypomagnesemia and this, associated with chronic hyperglycemia, may have enhanced oxidative stress. Erythrocyte magnesium may have contributed to prevent iron overload and worsening of oxidative stress and hyperglycemic status.

  1. Effect of iron oxide on nitrification in two agricultural soils with different pH

    Science.gov (United States)

    Huang, Xueru; Zhu-Barker, Xia; Horwath, William R.; Faeflen, Sarwee J.; Luo, Hongyan; Xin, Xiaoping; Jiang, Xianjun

    2016-10-01

    Iron (Fe) affects soil nitrogen (N) cycling processes both in anoxic and oxic environments. The role of Fe in soil N transformations including nitrification, mineralization, and immobilization, is influenced by redox activity, which is regulated by soil pH. The effect of Fe minerals, particularly oxides, on soil N transformation processes depends on soil pH, with Fe oxide often stimulating nitrification activity in the soil with low pH. We conducted lab incubations to investigate the effect of Fe oxide on N transformation rates in two subtropical agricultural soils with low pH (pH 5.1) and high pH (pH 7.8). 15N-labeled ammonium and nitrate were used separately to determine N transformation rates combined with Fe oxide (ferrihydrite) addition. Iron oxide stimulated net nitrification in low-pH soil (pH 5.1), while the opposite occurred in high-pH soil (pH 7.8). Compared to the control, Fe oxide decreased microbial immobilization of inorganic N by 50 % in low-pH soil but increased it by 45 % in high-pH soil. A likely explanation for the effects at low pH is that Fe oxide increased NH3-N availability by stimulating N mineralization and inhibiting N immobilization. These results indicate that Fe oxide plays an important role in soil N transformation processes and the magnitude of the effect of Fe oxide is dependent significantly on soil pH.

  2. Amoxicillin Oxidative Degradation Synthesized by Nano Zero Valent Iron

    Directory of Open Access Journals (Sweden)

    AR Yazdanbakhsh

    2016-03-01

    Full Text Available Introduction: Amoxicillin is one of the most important groups of pharmaceuticals that benefits humans and animals. However, antibiotics excertion in wastewaters and environment have emerged as a serious risk to the biotic environment, and their toxic effects can harm the organisms. Iron-based metallic nanoparticles have received special attention in regard with remediation of groundwater contaminants. In the typical nZVI-based bimetallic particle system, Fe acts as the reducing agent. Thus, the present study aimed to evaluate the synthesis and characteristics of nZVI in regard with degrading AMX. Methods: In this study, nZVI nanoparticles were synthesized using the liquid-phase reduction method by EDTA as a stabilizer material. Structure and properties of nanoparticles were characterized by BET, SEM, XRD and EDX analysis. A multi-variate analysis was applied using a response surface methodology (RSM in order to develop a quadratic model as a functional relationship between AMX removal efficiency and independent variables ( initial pH values, dosage of nZVI, contact time and amoxicillin concentration. The four independent variables of solution pH (2–10, AMX concentration (5-45mg/l, contact time (5-85 min and nanoparticles dose (0.25 – 1.25 g were transformed to the coded values. Results: The study results demonstrated that more than 69 % of AMX was removed by nZVI. The optimal AMX removal conditions using nZVI were found as 1.25 g of nZVI, pH 4, contact time of 80 min and concentration of 30 mg/l. Conclusions: The ability of nZVI in degradation of AMX revealed that these materials can serve as a potential nano material with respect to the environmental remediation.

  3. Synthesis, Characterization, and Evaluation of Boron-Doped Iron Oxides for the Photocatalytic Degradation of Atrazine under Visible Light

    Directory of Open Access Journals (Sweden)

    Shan Hu

    2012-01-01

    Full Text Available Photocatalytic degradation of atrazine by boron-doped iron oxides under visible light irradiation was investigated. In this work, boron-doped goethite and hematite were successfully prepared by sol-gel method with trimethylborate as boron precursor. The powders were characterized by XRD, UV-vis diffuse reflectance spectra, and porosimetry analysis. The results showed that boron doping could influence the crystal structure, enlarge the BET surface area, improve light absorption ability, and narrow their band-gap energy. The photocatalytic activity of B-doped iron oxides was evaluated in the degradation of atrazine under the visible light irradiation, and B-doped iron oxides showed higher atrazine degradation rate than that of pristine iron oxides. Particularly, B-doped goethite exhibited better photocatalytic activity than B-doped hematite.

  4. Correction: Polyol synthesis, functionalisation, and biocompatibility studies of superparamagnetic iron oxide nanoparticles as potential MRI contrast agents

    Science.gov (United States)

    Hachani, Roxanne; Lowdell, Mark; Birchall, Martin; Hervault, Aziliz; Mertz, Damien; Begin-Colin, Sylvie; Thanh, Nguy&Ecirtil; N. Thi&Cmb. B. Dot; Kim

    2016-02-01

    Correction for `Polyol synthesis, functionalisation, and biocompatibility studies of superparamagnetic iron oxide nanoparticles as potential MRI contrast agents' by Roxanne Hachani et al., Nanoscale, 2015, DOI: 10.1039/c5nr03867g.

  5. Iron-Mediated Lysosomal Membrane Permeabilization in Ethanol-Induced Hepatic Oxidative Damage and Apoptosis: Protective Effects of Quercetin.

    Science.gov (United States)

    Li, Yanyan; Chen, Man; Xu, Yanyan; Yu, Xiao; Xiong, Ting; Du, Min; Sun, Jian; Liu, Liegang; Tang, Yuhan; Yao, Ping

    2016-01-01

    Iron, in its free ferrous states, can catalyze Fenton reaction to produce OH∙, which is recognized as a crucial role in the pathogenesis of alcoholic liver diseases (ALD). As a result of continuous decomposition of iron-containing compounds, lysosomes contain a pool of redox-active iron. To investigate the important role of intralysosomal iron in alcoholic liver injury and the potential protection of quercetin, male C57BL/6J mice fed by Lieber De Carli diets containing ethanol (30% of total calories) were cotreated by quercetin or deferoxamine (DFO) for 15 weeks and ethanol-incubated mice primary hepatocytes were pretreated with FeCl3, DFO, and bafilomycin A1 at their optimal concentrations and exposure times. Chronic ethanol consumption caused an evident increase in lysosomal redox-active iron accompanying sustained oxidative damage. Iron-mediated ROS could trigger lysosomal membrane permeabilization (LMP) and subsequent mitochondria apoptosis. The hepatotoxicity was attenuated by reducing lysosomal iron while being exacerbated by escalating lysosomal iron. Quercetin substantially alleviated the alcoholic liver oxidative damage and apoptosis by decreasing lysosome iron and ameliorating iron-mediated LMP, which provided a new prospective of the use of quercetin against ALD.

  6. Iron-Mediated Lysosomal Membrane Permeabilization in Ethanol-Induced Hepatic Oxidative Damage and Apoptosis: Protective Effects of Quercetin

    Directory of Open Access Journals (Sweden)

    Yanyan Li

    2016-01-01

    Full Text Available Iron, in its free ferrous states, can catalyze Fenton reaction to produce OH∙, which is recognized as a crucial role in the pathogenesis of alcoholic liver diseases (ALD. As a result of continuous decomposition of iron-containing compounds, lysosomes contain a pool of redox-active iron. To investigate the important role of intralysosomal iron in alcoholic liver injury and the potential protection of quercetin, male C57BL/6J mice fed by Lieber De Carli diets containing ethanol (30% of total calories were cotreated by quercetin or deferoxamine (DFO for 15 weeks and ethanol-incubated mice primary hepatocytes were pretreated with FeCl3, DFO, and bafilomycin A1 at their optimal concentrations and exposure times. Chronic ethanol consumption caused an evident increase in lysosomal redox-active iron accompanying sustained oxidative damage. Iron-mediated ROS could trigger lysosomal membrane permeabilization (LMP and subsequent mitochondria apoptosis. The hepatotoxicity was attenuated by reducing lysosomal iron while being exacerbated by escalating lysosomal iron. Quercetin substantially alleviated the alcoholic liver oxidative damage and apoptosis by decreasing lysosome iron and ameliorating iron-mediated LMP, which provided a new prospective of the use of quercetin against ALD.

  7. Synthesis and Application of Carbon–Iron Oxide Microspheres’ Black Pigments in Electrophoretic Displays

    Directory of Open Access Journals (Sweden)

    Meng Xianwei

    2010-01-01

    Full Text Available Abstract Carbon–iron oxide microspheres’ black pigments (CIOMBs had been prepared via ultrasonic spray pyrolysis of aqueous solutions containing ferrous chloride and glucose. Due to the presence of carbon, CIOMBs not only exhibited remarkably acid resistance, but also could be well dispersed in both polar solvents and nonpolar solvent. Finally, dispersions of hollow CIOMBs in tetrachloroethylene had successfully been applied in electrophoretic displays.

  8. Lactate Oxidation Coupled to Iron or Electrode Reduction by Geobacter sulfurreducens PCA

    KAUST Repository

    Call, D. F.

    2011-10-14

    Geobacter sulfurreducens PCA completely oxidized lactate and reduced iron or an electrode, producing pyruvate and acetate intermediates. Compared to the current produced by Shewanella oneidensis MR-1, G. sulfurreducens PCA produced 10-times-higher current levels in lactate-fed microbial electrolysis cells. The kinetic and comparative analyses reported here suggest a prominent role of G. sulfurreducens strains in metaland electrode-reducing communities supplied with lactate. © 2011, American Society for Microbiology.

  9. Anaerobic oxidation of methane in an iron-rich Danish freshwater lake sediment

    DEFF Research Database (Denmark)

    Nordi, Katrin á; Thamdrup, Bo; Schubert, Carsten J.

    2013-01-01

    Freshwater systems are identified as one of the main natural methane sources, but little is known about the importance of anaerobic oxidation of methane (AOM) in these systems. We investigated AOM in a lake sediment characterized by a high reactive iron content, normal sulfate concentrations in t...... from freshwater sediments, and the finding of AOM at sulfate concentrations ancient low-sulfate oceans, than was previously appreciated....

  10. Biologically Inspired Design of Biocompatible Iron Oxide Nanoparticles for Biomedical Applications

    OpenAIRE

    Demirer, Gözde S.; Okur, Aysu C; Kızılel, Seda

    2015-01-01

    During the last couple of decades considerable research efforts have been directed towards the synthesis and coating of iron oxide nanoparticles (IONPs) for biomedical applications. To address the current limitations, recent studies have focused on the design of new generation nanoparticle systems whose internalization and targeting capabilities have been improved through surface modifications. This review covers the most recent challenges and advances in the development of IONPs with enhance...

  11. Massive Intracellular Biodegradation of Iron Oxide Nanoparticles Evidenced Magnetically at Single-Endosome and Tissue Levels.

    OpenAIRE

    MAZUEL, François; Espinosa, Ana; Luciani, Nathalie; Reffay, Myriam; Le Borgne, Rémi; Motte, Laurence; Desboeufs, Karine; Michel, Aude; Pellegrino, Teresa; Lalatonne, Yoann; Wilhelm, Claire

    2016-01-01

    International audience; Quantitative studies of the long-term fate of iron oxide nanoparticles inside cells, a prerequisite for regenerative medicine applications, are hampered by the lack of suitable biological tissue models and analytical methods. Here, we propose stem-cell spheroids as a tissue model to track intracellular magnetic nanoparticle transformations during long-term tissue maturation. We show that global spheroid magnetism can serve as a fingerprint of the degradation process, a...

  12. Magnetic properties of magnetic liquids with iron-oxide particles - the influence of anisotropy and interactions

    DEFF Research Database (Denmark)

    Johansson, C.; Hanson, M.; Pedersen, Michael Stanley

    1997-01-01

    Magnetic liquids containing iron-oxide particles were investigated by magnetization and Mossbauer measurements. The particles were shown to be maghemite with a spontanious saturation magentization Ms = 320 kA m-1 at 200 K and a normalized high-field susceptibility x/M0 = 5.1x10-6 mkA-1, practical......-field-cooled magnetization and isothermal remanence decay, is influenced by interactions and strongly dependent on the applied magnetic field....

  13. Macrophage preconditioning with synthetic malaria pigment reduces cytokine production via heme iron-dependent oxidative stress.

    Science.gov (United States)

    Taramelli, D; Recalcati, S; Basilico, N; Olliaro, P; Cairo, G

    2000-12-01

    Hemozoin (malaria pigment), a polymer of hematin (ferri-protoporphyrin IX) derived from hemoglobin ingested by intraerythrocytic plasmodia, modulates cytokine production by phagocytes. Mouse peritoneal macrophages (PM) fed with synthetic beta-hematin (BH), structurally identical to native hemozoin, no longer produce tumor necrosis factor alpha (TNFalpha) and nitric oxide (NO) in response to lipopolysaccharide (LPS). Impairment of NO synthesis is due to inhibition of inducible nitric oxide synthase (iNOS) production. BH-mediated inhibition of PM functions cannot be ascribed to iron release from BH because neither prevention by iron chelators nor down-regulation of iron-regulatory protein activity was detected. Inhibition appears to be related to pigment-induced oxidative stress because (a) thiol compounds partially restored PM functions, (b) heme oxygenase (HO-1) and catalase mRNA levels were up-regulated, and (c) free radicals production increased in BH-treated cells. The antioxidant defenses of the cells determine the response to BH: microglia cells, which show a lower extent of induction of HO-1 and catalase mRNAs and lower accumulation of oxygen radicals, are less sensitive to the inhibitory effect of BH on cytokine production. Results indicate that BH is resistant to degradation by HO-1 and that heme-iron mediated oxidative stress may contribute to malaria-induced immunosuppression. This study may help correlate the different clinical manifestations of malaria, ranging from uncomplicated to severe disease, with dysregulation of phagocyte functions and promote better therapeutic strategies to counteract the effects of hemozoin accumulation.

  14. Tissue Plasminogen Activator Binding to Superparamagnetic Iron Oxide Nanoparticle—Covalent Versus Adsorptive Approach

    Science.gov (United States)

    Friedrich, Ralf P.; Zaloga, Jan; Schreiber, Eveline; Tóth, Ildikó Y.; Tombácz, Etelka; Lyer, Stefan; Alexiou, Christoph

    2016-06-01

    Functionalized superparamagnetic iron oxide nanoparticles are frequently used to develop vehicles for drug delivery, hyperthermia, and photodynamic therapy and as tools used for magnetic separation and purification of proteins or for biomolecular imaging. Depending on the application, there are various possible covalent and non-covalent approaches for the functionalization of particles, each of them shows different advantages and disadvantages for drug release and activity at the desired location.

  15. Manipulating the dimensional assembly pattern and crystalline structures of iron oxide nanostructures with a functional polyolefin.

    Science.gov (United States)

    He, Qingliang; Yuan, Tingting; Wang, Yiran; Guleria, Abhishant; Wei, Suying; Zhang, Guoqi; Sun, Luyi; Liu, Jingjing; Yu, Jingfang; Young, David P; Lin, Hongfei; Khasanov, Airat; Guo, Zhanhu

    2016-01-28

    Controlled crystalline structures (α- and γ-phase) and assembly patterns (1-D, 2-D and 3-D) were achieved in the synthesized iron oxide (Fe2O3) nanoparticles (NPs) using polymeric surfactant-polypropylene grafted maleic anhydride (PP-g-MA) with different concentrations. In addition, the change of the crystalline structure from the α- and γ-phase also led to the significantly increased saturation magnetization and coercivity.

  16. High-temperature XRD study of thermally induced structural and chemical changes in iron oxide nanoparticles embedded in porous carbons

    Energy Technology Data Exchange (ETDEWEB)

    Schettino, M. A.; Freitas, J. C. C., E-mail: jairccfreitas@yahoo.com.b [Universidade Federal do Espirito Santo, Departamento de Fisica (Brazil); Morigaki, M. K. [Universidade Federal do Espirito Santo, Departamento de Quimica (Brazil); Nunes, E.; Cunha, A. G.; Passamani, E. C.; Emmerich, F. G. [Universidade Federal do Espirito Santo, Departamento de Fisica (Brazil)

    2010-10-15

    Magnetic carbon-based nanomaterials have promising applications in many fields owing to their biocompatibility and thermal/mechanical stability. This study describes a high-temperature X-ray diffraction (XRD) study of the chemical and structural transformations suffered by superparamagnetic iron oxide nanoparticles embedded in porous carbons. The nanoparticles were prepared from the decomposition of iron pentacarbonyl over porous carbons, resulting in nanometer-sized iron oxides homogeneously dispersed into the carbon matrix. The thermally induced changes in these materials were followed by in situ high-temperature XRD, using synchrotron radiation. The growing of the nanoparticles and of the carbon crystallites were first observed, followed by the reduction of the iron oxides to form {alpha}-Fe (at temperatures as low as 400 {sup o}C in some cases) and {gamma}-Fe(C). The temperatures at which these chemical reactions occurred were dependent on the total time spent on heating and on the nature of the iron oxides formed in the as prepared materials. A noticeably large thermal expansion coefficient was also observed for the iron oxide nanocrystals. The formation of austenitic iron, stabilized by the presence of carbon, was found to be only partially reversible upon cooling.

  17. Assembly and Succession of Iron Oxide Microbial Mat Communities in Acidic Geothermal Springs

    Directory of Open Access Journals (Sweden)

    Jacob P. Beam

    2016-02-01

    Full Text Available Biomineralized ferric oxide microbial mats are ubiquitous features on Earth, are common in hot springs of Yellowstone National Park (YNP, WY, USA, and form due to direct interaction between microbial and physicochemical processes. The overall goal of this study was to determine the contribution of different community members to the assembly and succession of acidic high-temperature Fe(III-oxide mat ecosystems. Spatial and temporal changes in Fe(III-oxide accretion and the abundance of relevant community members were monitored over 70 days using sterile glass microscope slides incubated in the outflow channels of two acidic geothermal springs (pH = 3 - 3.5; temperature = 68 - 75 °C in YNP. Hydrogenobaculum spp. were the most abundant taxon identified during early successional stages (4 - 40 d, and have been shown to oxidize arsenite, sulfide, and hydrogen coupled to oxygen reduction. Iron-oxidizing populations of Metallosphaera yellowstonensis were detected within 4 d, and reached steady-state levels within 14 - 30 d, corresponding to visible Fe(III-oxide accretion. Heterotrophic archaea colonized near 30 d, and emerged as the dominant functional guild after 70 d and in mature Fe(III-oxide mats (1 - 2 cm thick. First-order rate constants of Fe(III-oxide accretion ranged from 0.046 - 0.05 d-1, and in situ microelectrode measurements showed that the oxidation of Fe(II is limited by the diffusion of O2 into the Fe(III-oxide mat. The formation of microterracettes also implicated O2 as a major variable controlling microbial growth and subsequent mat morphology. The assembly and succession of Fe(III-oxide mat communities follows a repeatable pattern of colonization by lithoautotrophic organisms, and the subsequent growth of diverse organoheterotrophs. The unique geochemical signatures and micromorphology of extant biomineralized Fe(III-oxide mats are useful for understanding other Fe(II-oxidizing systems.

  18. Isolation of iron-oxidizing bacteria from corroded concretes of sewage treatment plants.

    Science.gov (United States)

    Maeda, T; Negishi, A; Komoto, H; Oshima, Y; Kamimura, K; Sugio, T

    1999-01-01

    Thirty-six strains of iron-oxidizing bacteria were isolated from corroded concrete samples obtained at eight sewage treatment plants in Japan. All of the strains isolated grew autotrophically in ferrous sulfate (3.0%), elemental sulfur (1.0%) and FeS (1.0%) media (pH 1.5). Washed intact cells of the 36 isolates had activities to oxidize both ferrous iron and elemental sulfur. Strain SNA-5, a representative of the isolated strains, was a gram-negative, rod-shaped bacterium (0.5-0.6x0.9-1.5 microm). The mean G+C content of its DNA was 55.9 mol%. The pH and temperature optima for growth were 1.5 and 30 degrees C, and the bacterium had activity to assimilate 14CO2 into the cells when ferrous iron or elemental sulfur was used as a sole source of energy. These results suggest that SNA-5 is Thiobacillus ferrooxidans strain. The pHs and numbers of iron-oxidizing bacteria in corroded concrete samples obtained by boring to depths of 0-1, 1-3, and 3-5 cm below the concrete surface were respectively 1.4, 1.7, and 2.0, and 1.2 x 10(8), 5 x 10(7), and 5 x 10(6) cells/g concrete. The degree of corrosion in the sample obtained nearest to the surface was more severe than in the deeper samples. The findings indicated that the levels of acidification and corrosion of the concrete structure corresponded with the number of iron-oxidizing bacteria in a concrete sample. Sulfuric acid produced by the chemolithoautotrophic sulfur-oxidizing bacterium Thiobacillus thiooxidansis known to induce concrete corrosion. Since not only T. thiooxidans but also T. ferrooxidans can oxidize reduced sulfur compounds and produce sulfuric acid, the results strongly suggest that T. ferrooxidans as well as T. thiooxidans is involved in concrete corrosion.

  19. Iron Phosphate Coating:A Novel Approach to Controlling Pyrite Oxidation

    Institute of Scientific and Technical Information of China (English)

    HUANGXIAO; V.P.EVANGELOU

    1997-01-01

    A novel coating technique was develped for controlling pyrite oxidation .The technique involved leaching pyrite particles with a solution containing low concentrations of phosphate and hydrogen peroxide.During the leaching rpocess,the iron released from pyrite by hydrogen proxide was precipitated by phosphate as a ferric phosphate coating .This coating was shown to be able to effectively prevent pyirte from oxidation and it could be established at the expense of only surface portions of pyrite.The emergence of this technique could provide a unique potential route for abating acid mine draingage and reclaiming sulfide-containing degraded mining land.

  20. Oxidative stress and iron imbalance in Alzheimer disease: how rust became the fuss!

    Science.gov (United States)

    Smith, Mark A

    2006-01-01

    The role of oxidative stress in the pathogenesis of Alzheimer disease has gone from epiphenomena to phenomena. This transition, from disregarded to accepted theory, started in the early-mid 1990s and was accelerated by a number of reports in the literature showing that redox-active sources of transition metals, such as iron, were increased in the brain at early stages of disease. As such, it became apparent that not only was there damage but, more importantly, the machinery to exact such damage was ever present. In this review, the author chronicles his personal perspective on the past, present, and future of oxidative stress in Alzheimer disease.

  1. Optimization of preparation of chitosan-coated iron oxide nanoparticles for biomedical applications by chemometrics approaches

    Science.gov (United States)

    Honary, Soheila; Ebrahimi, Pouneh; Rad, Hossein Asgari; Asgari, Mahsa

    2013-08-01

    Functionalized magnetic nanoparticles are used in several biomedical applications, such as drug delivery, magnetic cell separation, and magnetic resonance imaging. Size and surface properties of iron oxide nanoparticles are the two important factors which could dramatically affect the nanoparticle efficiency as well as their stability. In this study, the chemometrics approach was applied to optimize the coating process of iron oxide nanoparticles. To optimize the size of nanoparticles, the effect of two experimental parameters on size was investigated by means of multivariate analysis. The factors considered were chitosan molecular weight and chitosan-to-tripolyphosphate concentration ratio. The experiments were performed according to face-centered cube central composite response surface design. A second-order regression model was obtained which characterized by both descriptive and predictive abilities. The method was optimized with respect to the percent of Z average diameter's increasing after coating as response. It can be concluded that experimental design provides a suitable means of optimizing and testing the robustness of iron oxide nanoparticle coating method.

  2. Reduced Staphylococcus aureus biofilm formation in the presence of chitosan-coated iron oxide nanoparticles.

    Science.gov (United States)

    Shi, Si-Feng; Jia, Jing-Fu; Guo, Xiao-Kui; Zhao, Ya-Ping; Chen, De-Sheng; Guo, Yong-Yuan; Zhang, Xian-Long

    Staphylococcus aureus can adhere to most foreign materials and form biofilm on the surface of medical devices. Biofilm infections are difficult to resolve. The goal of this in vitro study was to explore the use of chitosan-coated nanoparticles to prevent biofilm formation. For this purpose, S. aureus was seeded in 96-well plates to incubate with chitosan-coated iron oxide nanoparticles in order to study the efficiency of biofilm formation inhibition. The biofilm bacteria count was determined using the spread plate method; biomass formation was measured using the crystal violet staining method. Confocal laser scanning microscopy and scanning electron microscopy were used to study the biofilm formation. The results showed decreased viable bacteria numbers and biomass formation when incubated with chitosan-coated iron oxide nanoparticles at all test concentrations. Confocal laser scanning microscopy showed increased dead bacteria and thinner biofilm when incubated with nanoparticles at a concentration of 500 µg/mL. Scanning electron microscopy revealed that chitosan-coated iron oxide nanoparticles inhibited biofilm formation in polystyrene plates. Future studies should be performed to study these nanoparticles for anti-infective use.

  3. Iron oxide nanoparticles stabilized with a bilayer of oleic acid for magnetic hyperthermia and MRI applications

    Energy Technology Data Exchange (ETDEWEB)

    Soares, Paula I.P. [i3N/CENIMAT, Department of Materials Science, Faculty of Science and Technology, Universidade NOVA de Lisboa, Campus de Caparica, 2829-516 Caparica (Portugal); Laia, César A.T. [Laboratório Associado para a Química Verde (LAQV), REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, FCT, Universidade Nova de Lisboa, 2829-516 Caparica (Portugal); Carvalho, Alexandra [i3N/CENIMAT, Department of Materials Science, Faculty of Science and Technology, Universidade NOVA de Lisboa, Campus de Caparica, 2829-516 Caparica (Portugal); Pereira, Laura C.J.; Coutinho, Joana T. [C2TN, Instituto Superior Técnico, Universidade de Lisboa, Estrada Nacional 10, ao km 139,7, 2695-066 Bobadela LRS (Portugal); Ferreira, Isabel M.M., E-mail: imf@fct.unl.pt [i3N/CENIMAT, Department of Materials Science, Faculty of Science and Technology, Universidade NOVA de Lisboa, Campus de Caparica, 2829-516 Caparica (Portugal); Novo, Carlos M.M. [Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, IHMT/UNL, 1349-008 Lisboa (Portugal); Borges, João Paulo, E-mail: jpb@fct.unl.pt [i3N/CENIMAT, Department of Materials Science, Faculty of Science and Technology, Universidade NOVA de Lisboa, Campus de Caparica, 2829-516 Caparica (Portugal)

    2016-10-15

    Highlights: • Superparamagnetic iron oxide nanoparticles were stabilized with oleic acid. • Maximum stabilization was achieved at neutral pH. • Magnetic resonance imaging and magnetic hyperthermia applications were tested. • The produced nanoparticles are viable for both biomedical applications. - Abstract: Iron oxide nanoparticles (Fe{sub 3}O{sub 4}, IONPs) are promising candidates for several biomedical applications such as magnetic hyperthermia and as contrast agents for magnetic resonance imaging (MRI). However, their colloidal stability in physiological conditions hinders their application requiring the use of biocompatible surfactant agents. The present investigation focuses on obtaining highly stable IONPs, stabilized by the presence of an oleic acid bilayer. Critical aspects such as oleic acid concentration and pH were optimized to ensure maximum stability. NPs composed of an iron oxide core with an average diameter of 9 nm measured using transmission electron microscopy (TEM) form agglomerates with an hydrodynamic diameter of around 170 nm when dispersed in water in the presence of an oleic acid bilayer, remaining stable (zeta potential of −120 mV). Magnetic hyperthermia and the relaxivities measurements show high efficiency at neutral pH which enables their use for both magnetic hyperthermia and MRI.

  4. Impact of Oxidative Stress in Premature Aging and Iron Overload in Hemodialysis Patients

    Science.gov (United States)

    Hernández Vázquez, Wendy Ivett; Solorio-Meza, Sergio; Albarrán-Tamayo, Froylán; Ramos-Rodríguez, Edna; Benítez- Bribiesca, Luis

    2016-01-01

    Background. Increased oxidative stress is a well described feature of patients in hemodialysis. Their need for multiple blood transfusions and supplemental iron causes a significant iron overload that has recently been associated with increased oxidation of polyunsaturated lipids and accelerated aging due to DNA damage caused by telomere shortening. Methods. A total of 70 patients were evaluated concomitantly, 35 volunteers with ferritin levels below 500 ng/mL (Group A) and 35 volunteers with ferritin levels higher than 500 ng/mL (Group B). A sample of venous blood was taken to extract DNA from leukocytes and to measure relative telomere length by real-time PCR. Results. Patients in Group B had significantly higher plasma TBARS (p = 0.008), carbonyls (p = 0.0004), and urea (p = 0.02) compared with those in Group A. Telomeres were significantly shorter in Group B, 0.66 (SD, 0.051), compared with 0.75 (SD, 0.155) in Group A (p = 0.0017). We observed a statistically significant association between relative telomere length and ferritin levels (r = −0.37, p = 0.001). Relative telomere length was inversely related to time on hemodialysis (r = −0.27, p = 0.02). Conclusions. Our findings demonstrate that iron overload was associated with increased levels of oxidative stress and shorter relative telomere length. PMID:27800120

  5. New findings about iron oxide nanoparticles and their different effects on murine primary brain cells.

    Science.gov (United States)

    Neubert, Jenni; Wagner, Susanne; Kiwit, Jürgen; Bräuer, Anja U; Glumm, Jana

    2015-01-01

    The physicochemical properties of superparamagnetic iron oxide nanoparticles (SPIOs) enable their application in the diagnostics and therapy of central nervous system diseases. However, since crucial information regarding side effects of particle-cell interactions within the central nervous system is still lacking, we investigated the influence of novel very small iron oxide particles or the clinically approved ferucarbotran or ferumoxytol on the vitality and morphology of brain cells. We exposed primary cell cultures of microglia and hippocampal neurons, as well as neuron-glia cocultures to varying concentrations of SPIOs for 6 and/or 24 hours, respectively. Here, we show that SPIO accumulation by microglia and subsequent morphological alterations strongly depend on the respective nanoparticle type. Microglial viability was severely compromised by high SPIO concentrations, except in the case of ferumoxytol. While ferumoxytol did not cause immediate microglial death, it induced severe morphological alterations and increased degeneration of primary neurons. Additionally, primary neurons clearly degenerated after very small iron oxide particle and ferucarbotran exposure. In neuron-glia cocultures, SPIOs rather stimulated the outgrowth of neuronal processes in a concentration- and particle-dependent manner. We conclude that the influence of SPIOs on brain cells not only depends on the particle type but also on the physiological system they are applied to.

  6. Colloidal stability of iron oxide nanocrystals coated with a PEG-based tetra-catechol surfactant

    Science.gov (United States)

    Mondini, Sara; Drago, Carmelo; Ferretti, Anna M.; Puglisi, Alessandra; Ponti, Alessandro

    2013-03-01

    Long-term colloidal stability of magnetic iron oxide nanoparticles (NPs) is an important goal that has not yet been fully achieved. To make an advance in our understanding of the colloidal stability of iron oxide NPs in aqueous media, we prepared NPs comprising a monodisperse (13 nm) iron oxide core coated with a PEG-based (PEG: polyethyleneglycol) surfactant. This consists of a methoxy-terminated PEG chain (MW = 5000 Da) bearing four catechol groups via a diethylenetriamine linker. The surfactant was grafted onto the nanocrystals by ligand exchange monitored by infrared spectroscopy. The colloidal stability of these nanoparticles was probed by monitoring the time evolution of the Z-average intensity-weighted radius Rh and volume-weighted size distribution Pv obtained from analysis of dynamic light scattering data. The nanoparticles showed no sign of aggregation for four months in deionized water at room temperature and also when subjected to thermal cycling between 25 and 75 °C. In 0.01 M PBS (phosphate buffered saline), aggregation (if any) is slow and partial; after 66 h, about 50% of NPs have not aggregated. Aggregation is more effective in 0.15 M NH4AcO buffer, where isolated particles are not observed after 66 h, and especially in acidic NH4AcO/AcOH buffer, where aggregation is complete within 1 h and precipitation is observed. The differing stability of the NPs in the above aqueous media is closely related to their ζ potential.

  7. Magnetically stimulated ciprofloxacin release from polymeric microspheres entrapping iron oxide nanoparticles

    Directory of Open Access Journals (Sweden)

    Sirivisoot S

    2015-07-01

    Full Text Available Sirinrath Sirivisoot,1 Benjamin S Harrison2 1Biological Engineering Program, Faculty of Engineering, King Mongkut’s University of Technology Thonburi, Bangkok, Thailand; 2Wake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine, Wake Forest University Health Sciences, Winston-Salem, NC, USA Abstract: To extend the external control capability of drug release, iron oxide nanoparticles (NPs encapsulated into polymeric microspheres were used as magnetic media to stimulate drug release using an alternating magnetic field. Chemically synthesized iron oxide NPs, maghemite or hematite, and the antibiotic ciprofloxacin were encapsulated together within polycaprolactone microspheres. The polycaprolactone microspheres entrapping ciprofloxacin and magnetic NPs could be triggered for immediate drug release by magnetic stimulation at a maximum value of 40%. Moreover, the microspheres were cytocompatible with fibroblasts in vitro with a cell viability percentage of more than 100% relative to a nontreated control after 24 hours of culture. Macrophage cell cultures showed no signs of increased inflammatory responses after in vitro incubation for 56 hours. Treatment of Staphylococcus aureus with the magnetic microspheres under an alternating (isolating magnetic field increased bacterial inhibition further after 2 days and 5 days in a broth inhibition assay. The findings of the present study indicate that iron oxide NPs, maghemite and hematite, can be used as media for stimulation by an external magnetic energy to activate immediate drug release. Keywords: antibacterial, maghemite, hematite, Staphylococcus aureus

  8. Effect of magnetic field on the zero valent iron induced oxidation reaction.

    Science.gov (United States)

    Kim, Dong-hyo; Kim, Jungwon; Choi, Wonyong

    2011-08-30

    The magnetic field (MF) effect on the zero valent iron (ZVI) induced oxidative reaction was investigated for the first time. The degradation of 4-chlorophenol (4-CP) in the ZVI system was employed as the test oxidative reaction. MF markedly enhanced the degradation of 4-CP with the concurrent production of chlorides. The consumption of dissolved O(2) by ZVI reaction was also enhanced in the presence of MF whereas the competing reaction of H(2) production from proton reduction was retarded. Since the ZVI-induced oxidation is mainly driven by the in situ generated hydroxyl radicals, the production of OH radicals was monitored by the spin trap method using electron spin resonance (ESR) spectroscopy. It was confirmed that the concentration of trapped OH radicals was enhanced in the presence of MF. Since both O(2) and Fe(0) are paramagnetic, the diffusion of O(2) onto the iron surface might be accelerated under MF. The magnetized iron can attract oxygen on itself, which makes the mass transfer process faster. As a result, the surface electrochemical reaction between Fe(0) and O(2) can be accelerated with the enhanced production of OH radicals. MF might retard the recombination of OH radicals as well.

  9. Magnetic Iron Oxide Nanoparticles Mediated Gene Therapy for Cancer An In Vitro Study

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The aim of this study was to evaluate the feasibility and efficacy of using TRAIL gene to treat breast cancer mediated with a novel carrier - magnetic iron oxide nanoparticles (polyMAG-1000) coated with PEI. The magnetic iron oxide nanoparticles were used as gene carrier to transfect TRAIL gene into MCF-7 cells. The polyMAG-1000 without TRAIL gene was transfected into the tumor cells as negative control. TRAIL gene transfection with liposome as carrier served as positive control. The apoptosis of cells was detected with TUNEL method. The apoptosis ratio of tumor cells was measured with flow cytometry (FCM). It was found that the apoptosis occurred in the tumor cells after transfection of TRAIL gene mediated by both polyMAG-1000 and liposome. The apoptosis ratio in the group with polyMAG-1000 as gene carrier was (25.11±2.85) %, whereas it was (5.06±1.05) % in the control group with polyMAG-1000 (P<0.01). The apoptosis ratio was as low as (18.31±2.44) % in the group with liposome as gene carrier (P<0.05, as compared with the group with polyMAG-1000 as gene carrier). It is suggested that TRAIL gene may induce apoptosis in MCF-7 breast cancer cells. The magnetic iron oxide nanoparticles coated with PEI may be a potential gene carrier with high transfection efficacy for cancer gene therapy.

  10. Magnetic Properties of Polyvinyl Alcohol and Doxorubicine Loaded Iron Oxide Nanoparticles for Anticancer Drug Delivery Applications.

    Directory of Open Access Journals (Sweden)

    Muhammad Nadeem

    Full Text Available The current study emphasizes the synthesis of iron oxide nanoparticles (IONPs and impact of hydrophilic polymer polyvinyl alcohol (PVA coating concentration as well as anticancer drug doxorubicin (DOX loading on saturation magnetization for target drug delivery applications. Iron oxide nanoparticles particles were synthesized by a reformed version of the co-precipitation method. The coating of polyvinyl alcohol along with doxorubicin loading was carried out by the physical immobilization method. X-ray diffraction confirmed the magnetite (Fe3O4 structure of particles that remained unchanged before and after polyvinyl alcohol coating and drug loading. Microstructure and morphological analysis was carried out by transmission electron microscopy revealing the formation of nanoparticles with an average size of 10 nm with slight variation after coating and drug loading. Transmission electron microscopy, energy dispersive, and Fourier transform infrared spectra further confirmed the conjugation of polymer and doxorubicin with iron oxide nanoparticles. The room temperature superparamagnetic behavior of polymer-coated and drug-loaded magnetite nanoparticles were studied by vibrating sample magnetometer. The variation in saturation magnetization after coating evaluated that a sufficient amount of polyvinyl alcohol would be 3 wt. % regarding the externally controlled movement of IONPs in blood under the influence of applied magnetic field for in-vivo target drug delivery.

  11. Rapid microwave-assisted synthesis of dextran-coated iron oxide nanoparticles for magnetic resonance imaging

    Science.gov (United States)

    Osborne, Elizabeth A.; Atkins, Tonya M.; Gilbert, Dustin A.; Kauzlarich, Susan M.; Liu, Kai; Louie, Angelique Y.

    2012-06-01

    Currently, magnetic iron oxide nanoparticles are the only nanosized magnetic resonance imaging (MRI) contrast agents approved for clinical use, yet commercial manufacturing of these agents has been limited or discontinued. Though there is still widespread demand for these particles both for clinical use and research, they are difficult to obtain commercially, and complicated syntheses make in-house preparation unfeasible for most biological research labs or clinics. To make commercial production viable and increase accessibility of these products, it is crucial to develop simple, rapid and reproducible preparations of biocompatible iron oxide nanoparticles. Here, we report a rapid, straightforward microwave-assisted synthesis of superparamagnetic dextran-coated iron oxide nanoparticles. The nanoparticles were produced in two hydrodynamic sizes with differing core morphologies by varying the synthetic method as either a two-step or single-step process. A striking benefit of these methods is the ability to obtain swift and consistent results without the necessity for air-, pH- or temperature-sensitive techniques; therefore, reaction times and complex manufacturing processes are greatly reduced as compared to conventional synthetic methods. This is a great benefit for cost-effective translation to commercial production. The nanoparticles are found to be superparamagnetic and exhibit properties consistent for use in MRI. In addition, the dextran coating imparts the water solubility and biocompatibility necessary for in vivo utilization.

  12. Use of iron oxide magnetic nanosorbents for Cr (VI removal from aqueous solutions: A review

    Directory of Open Access Journals (Sweden)

    Nirmala Ilankoon

    2014-10-01

    Full Text Available This review paper focuses on the use of iron oxide nanosorbents for the removal of hexavalent Chromium [Cr(VI], from aqueous media. Cr(VI is a well-known toxic heavy metal, which can cause severe damages to the human health even with the presence of trace levels. Chromium continuously enters into water streams from different sources. Several methods are available for Cr(VI removal and some of them are well established in industrial scale whilst some are still in laboratory scale. Reduction followed by chemical precipitation, adsorption, electro-kinetic remediation, membrane separation processes and bioremediation are some of the removal techniques. Each method is associated with both advantages and disadvantages. Currently, the use of nanosorbents for the aqueous chromium removal is popular among researchers and iron oxide nanoparticles are the most frequently used nanosorbents. This review paper summarizes the performance of different iron oxide nanosorbents studied on the last decade. The direct comparison of these results is difficult due to different experimental conditions used in each study. Adsorption isotherms and adsorption kinetics models are also discussed in this review paper. The effect of solution pH, temperature, initial Cr(VI concentration, adsorbent dosage and other coexisting ions are also briefly discussed. From the results it is evident that, more attention needs to be paid on the industrial application of the technologies which were successful in the laboratory scale.

  13. Diversity of iron oxidizers in wetland soils revealed by novel 16S rRNA primers targeting Gallionella-related bacteria

    NARCIS (Netherlands)

    Wang, J.; Muyzer, G.; Bodelier, P.L.E.; Laanbroek, R.

    2009-01-01

    Neutrophilic iron-oxidizing bacteria (FeOB) are important catalysts of iron cycling in wetland environments. However, little is known about their diversity and distribution in various environments. The aim of this study was to develop a PCR-DGGE assay enabling the detection of neutrophilic iron oxid

  14. Morphology-controlled growth of magnet