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Sample records for mineral titanium phosphate

  1. Radioactivity of phosphate mineral products

    OpenAIRE

    Mitrović Branislava; Vitorović Gordana; Stojanović Mirjana; Vitorović Duško

    2011-01-01

    The phosphate industry is one of the biggest polluters of the environment with uranium. Different products are derived after processing phosphoric ore, such as mineral and phosphate fertilizers and phosphate mineral supplements (dicalcium-and monocalcium phosphate) for animal feeding. Phosphate mineral additives used in animal food may contain a high activity of uranium. Research in this study should provide an answer to the extent in which phosphate minera...

  2. Synthesis and controllable wettability of micro- and nanostructured titanium phosphate thin films formed on titanium plates.

    Science.gov (United States)

    Yada, Mitsunori; Inoue, Yuko; Sakamoto, Ayako; Torikai, Toshio; Watari, Takanori

    2014-05-28

    The hydrothermal treatment of a titanium plate in a mixed aqueous solution of hydrogen peroxide and aqueous phosphoric acid under different conditions results in the formation of various titanium phosphate thin films. The films have various crystal structures such as Ti2O3(H2PO4)2·2H2O, α-titanium phosphate (Ti(HPO4)2·H2O), π-titanium phosphate (Ti2O(PO4)2·H2O), or low-crystallinity titanium phosphate and different morphologies that have not been previously reported such as nanobelts, microflowers, nanosheets, nanorods, or nanoplates. The present study also suggests the mechanisms behind the formation of these thin films. The crystal structure and morphology of the titanium phosphate thin films depend strongly on the concentration of the aqueous hydrogen peroxide solution, the amount of phosphoric acid, and the reaction temperature. In particular, hydrogen peroxide plays an important role in the formation of the titanium phosphate thin films. Moreover, controllable wettability of the titanium phosphate thin films, including superhydrophilicity and superhydrophobicity, is reported. Superhydrophobic surfaces with controllable adhesion to water droplets are obtained on π-titanium phosphate nanorod thin films modified with alkylamine molecules. The adhesion force between a water droplet and the thin film depends on the alkyl chain length of the alkylamine and the duration of ultraviolet irradiation utilized for photocatalytic degradation.

  3. Mineral induced formation of sugar phosphates

    Science.gov (United States)

    Pitsch, S.; Eschenmoser, A.; Gedulin, B.; Hui, S.; Arrhenius, G.

    1995-01-01

    Glycolaldehyde phosphate, sorbed from highly dilute, weakly alkaline solution into the interlayer of common expanding sheet structure metal hydroxide minerals, condenses extensively to racemic aldotetrose-2, 4-diphophates, and aldohexose-2, 4, 6-triphosphates. The reaction proceeds mainly through racemic erythrose-2, 4-phosphate, and terminates with a large fraction of racemic altrose-2, 4, 6-phosphate. In the absence of an inductive mineral phase, no detectable homogeneous reaction takes place in the concentration- and pH range used. The reactant glycolaldehyde phosphate is practically completely sorbed within an hour from solutions with concentrations as low as 50 micron; the half-time for conversion to hexose phosphates is of the order of two days at room temperature and pH 9.5. Total production of sugar phosphates in the mineral interlayer is largely independent of the glycolaldehyde phosphate concentration in the external solution, but is determined by the total amount of GAP offered for sorption up to the capacity of the mineral. In the presence of equimolar amounts of rac-glyceraldehyde-2-phosphate, but under otherwise similar conditions, aldopentose-2, 4, -diphosphates also form, but only as a small fraction of the hexose-2, 4, 6-phosphates.

  4. TUCS/phosphate mineralization of actinides

    Energy Technology Data Exchange (ETDEWEB)

    Nash, K.L. [Argonne National Lab., IL (United States)

    1997-10-01

    This program has as its objective the development of a new technology that combines cation exchange and mineralization to reduce the concentration of heavy metals (in particular actinides) in groundwaters. The treatment regimen must be compatible with the groundwater and soil, potentially using groundwater/soil components to aid in the immobilization process. The delivery system (probably a water-soluble chelating agent) should first concentrate the radionuclides then release the precipitating anion, which forms thermodynamically stable mineral phases, either with the target metal ions alone or in combination with matrix cations. This approach should generate thermodynamically stable mineral phases resistant to weathering. The chelating agent should decompose spontaneously with time, release the mineralizing agent, and leave a residue that does not interfere with mineral formation. For the actinides, the ideal compound probably will release phosphate, as actinide phosphate mineral phases are among the least soluble species for these metals. The most promising means of delivering the precipitant would be to use a water-soluble, hydrolytically unstable complexant that functions in the initial stages as a cation exchanger to concentrate the metal ions. As it decomposes, the chelating agent releases phosphate to foster formation of crystalline mineral phases. Because it involves only the application of inexpensive reagents, the method of phosphate mineralization promises to be an economical alternative for in situ immobilization of radionuclides (actinides in particular). The method relies on the inherent (thermodynamic) stability of actinide mineral phases.

  5. Effects of inositol phosphates on mineral utilization

    Energy Technology Data Exchange (ETDEWEB)

    Tao, S.H.; Fox, M.R.S.; Phillippy, B.Q.; Fry, B.E. Jr.; Johnson, M.L.; Johnston, M.R.

    1986-03-05

    The present study was designed to compare the effects of inositol tri-, tetra-, and pentaphosphate (IP3, IP4, and IP5) with those of phytic acid (IP6) on growth, development and mineral utilization of young quail. Day-old Japanese quail were fed a purified casein-gelatin control diet containing 20 ppm Zn with 0 or 8.33 mmoles/kg of each inositol phosphate, corresponding to 0.55% of IP6, for a week. As compared with controls, IP6 caused reduced body weight, poor feathering, severe perosis, decreased tibia Zn and ash, and decreased pancreas Zn and liver Mn. IP5 produced all the same adverse effects and tissue mineral changes as those by phytic acid, whereas birds fed IP3 or IP4 were normal. Moreover, IP3 and IP4 caused an increased tibia weight and ash. None of the above effects was produced by feeding inositol or inorganic phosphate. In a second experiment, the inositol phosphates were fed at either 8.33 or 16.66 mmoles/kg diet. Doubling inositol phosphate levels resulted in similar effects as those observed previously. Additionally, IP4 decreased pancreas Zn and IP3 increased tibia Zn. These results indicate that unlike IP6 and IP5, inositol phosphates with 4 or fewer phosphate groups, which can arise from hydrolysis of phytic acid during food processing, have very minor adverse effects but may be beneficial for bone mineralization.

  6. Hybrid Calcium Phosphate Coatings for Titanium Implants

    Science.gov (United States)

    Kharapudchenko, E.; Ignatov, V.; Ivanov, V.; Tverdokhlebov, S.

    2017-01-01

    Hybrid multilayer coatings were obtained on titanium substrates by the combination of two methods: the micro-arc oxidation in phosphoric acid solution with the addition of calcium compounds to high supersaturated state and RF magnetron sputtering of the target made of synthetic hydroxyapatite. 16 different groups of coatings were formed on titanium substrates and in vitro studies were conducted in accordance with ISO 23317 in the solution simulating body fluid. The studies using SEM, XRD of the coatings of the samples before and after exposure to SBF were performed. The features of morphology, chemical and phase composition of the studied coatings are shown.

  7. Expression of Phosphate Transporters during Dental Mineralization.

    Science.gov (United States)

    Merametdjian, L; Beck-Cormier, S; Bon, N; Couasnay, G; Sourice, S; Guicheux, J; Gaucher, C; Beck, L

    2017-09-01

    The importance of phosphate (Pi) as an essential component of hydroxyapatite crystals suggests a key role for membrane proteins controlling Pi uptake during mineralization in the tooth. To clarify the involvement of the currently known Pi transporters (Slc17a1, Slc34a1, Slc34a2, Slc34a3, Slc20a1, Slc20a2, and Xpr1) during tooth development and mineralization, we determined their spatiotemporal expression in murine tooth germs from embryonic day 14.5 to postnatal day 15 and in human dental samples from Nolla stages 6 to 9. Using real-time polymerase chain reaction, in situ hybridization, immunohistochemistry, and X-gal staining, we showed that the expression of Slc17a1, Slc34a1, and Slc34a3 in tooth germs from C57BL/6 mice were very low. In contrast, Slc34a2, Slc20a1, Slc20a2, and Xpr1 were highly expressed, mostly during the postnatal stages. The expression of Slc20a2 was 2- to 10-fold higher than the other transporters. Comparable results were obtained in human tooth germs. In mice, Slc34a2 and Slc20a1 were predominantly expressed in ameloblasts but not odontoblasts, while Slc20a2 was detected neither in ameloblasts nor in odontoblasts. Rather, Slc20a2 was highly expressed in the stratum intermedium and the subodontoblastic cell layer. Although Slc20a2 knockout mice did not show enamel defects, mutant mice showed a disrupted dentin mineralization, displaying unmerged calcospherites at the mineralization front. This latter phenotypical finding raises the possibility that Slc20a2 may play an indirect role in regulating the extracellular Pi availability for mineralizing cells rather than a direct role in mediating Pi transport through mineralizing plasma cell membranes. By documenting the spatiotemporal expression of Pi transporters in the tooth, our data support the possibility that the currently known Pi transporters may be dispensable for the initiation of dental mineralization and may rather be involved later during the tooth mineralization scheme.

  8. Characterization and in vitro biological evaluation of mineral/osteogenic growth peptide nanocomposites synthesized biomimetically on titanium

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Cen; Kong, Xiangdong [Bio-X Center, College of Life Sciences, Zhejiang Sci-Tech University, Hangzhou 310018 (China); Zhang, Sheng-Min [Advanced Biomaterials and Tissue Engineering Center, Huazhong University of Science and Technology, Wuhan 430074 (China); Lee, In-Seop, E-mail: inseop@yonsei.ac.kr [Bio-X Center, College of Life Sciences, Zhejiang Sci-Tech University, Hangzhou 310018 (China); Institute of Natural Sciences, Yonsei University, Seoul 120-749 (Korea, Republic of)

    2015-04-15

    Graphical abstract: - Highlights: • Mineral/OGP nanocomposite layers were synthesized biomimetically on Ti substrates. • Incorporated OGP affected the morphology and ultimate structure of mineral. • Incorporated OGP improved the MSCs adhesion, proliferation, and ALP activity. - Abstract: Nanocomposite layers of mineral/osteogenic growth peptide (OGP) were synthesized on calcium phosphate coated titanium substrates by immersing in calcium-phosphate buffer solution containing OGP. Peptide incorporated mineral was characterized by determining quantity loaded, effects on mineral morphology and structure. Also, the biological activity was investigated by cell adhesion, proliferation assay, and measurement of alkaline phosphatase (ALP) activity. X-ray photoelectron spectroscopy (XPS) and micro-bicinchoninic acid (BCA) assay revealed that OGP was successfully incorporated with mineral and the amount was increased with immersion time. Incorporated OGP changed the mineral morphology from sharp plate-like shape to more rounded one, and the octacalcium phosphate structure of the mineral was gradually transformed into apatite. With confocal microscopy to examine the incorporation of fluorescently labeled peptide, OGP was evenly distributed throughout mineral layers. Mineral/OGP nanocomposites promoted cell adhesion and proliferation, and also increased ALP activity of mesenchymal stem cells (MSCs). Results presented here indicated that the mineral/OGP nanocomposites formed on titanium substrates had the potential for applications in dental implants.

  9. Characterization and in vitro biological evaluation of mineral/osteogenic growth peptide nanocomposites synthesized biomimetically on titanium

    Science.gov (United States)

    Chen, Cen; Kong, Xiangdong; Zhang, Sheng-Min; Lee, In-Seop

    2015-04-01

    Nanocomposite layers of mineral/osteogenic growth peptide (OGP) were synthesized on calcium phosphate coated titanium substrates by immersing in calcium-phosphate buffer solution containing OGP. Peptide incorporated mineral was characterized by determining quantity loaded, effects on mineral morphology and structure. Also, the biological activity was investigated by cell adhesion, proliferation assay, and measurement of alkaline phosphatase (ALP) activity. X-ray photoelectron spectroscopy (XPS) and micro-bicinchoninic acid (BCA) assay revealed that OGP was successfully incorporated with mineral and the amount was increased with immersion time. Incorporated OGP changed the mineral morphology from sharp plate-like shape to more rounded one, and the octacalcium phosphate structure of the mineral was gradually transformed into apatite. With confocal microscopy to examine the incorporation of fluorescently labeled peptide, OGP was evenly distributed throughout mineral layers. Mineral/OGP nanocomposites promoted cell adhesion and proliferation, and also increased ALP activity of mesenchymal stem cells (MSCs). Results presented here indicated that the mineral/OGP nanocomposites formed on titanium substrates had the potential for applications in dental implants.

  10. Phosphate mineral formation on the supported dipalmitoylphosphatidylcholine (DPPC) layers.

    Science.gov (United States)

    Szcześ, Aleksandra

    2014-07-01

    Dipalmitoylphosphatidylcholine (DPPC) mono- and bilayers supported on mica surface were soaked for two weeks in a simulated body fluid (SBF) with ion concentrations nearly equal to those of human blood plasma. Two solutions were investigated: with and without Tris. The experiment was conducted at 20°C and at a physiological temperature equal to 37°C. Raman spectroscopy was used for the characterization of the precipitated phosphate minerals. These studies may provide information about the physiological mineralization of cell membranes that are mainly composed of phospholipids. Findings from these experiments suggest that the DPPC bilayers enhance the formation of less soluble phosphate forms especially at a temperature of 37°C. In the solution without Tris temperature increase gives more mineral deposits. It is probably the hydrogen interactions between phosphate groups of the phospholipid and hydroxyl groups from Tris that lower exposure of the phosphate group to interact with calcium ions.

  11. Pathogenic Mineralization of Calcium Phosphate on Human Heart Valves

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    When calcium phosphate forms in soft tissues such as blood vessels and heart valves, it causes disease. The abnormal formation of calcium phosphate is called pathogenic mineralization or pathogenic calcification. Cases of rheumatic heart disease (RHD) always occur with fibrotic and calcified tissue of heart valve. In this article, samples taken from calcified human heart valves were studied. The characterization was performed by scanning electronic micrascope, X-ray Diffraction and transmission electron microscopy with selective diffraction patterns. It is found for the first time that calcium phosphate grains existing in the calcified human heart valves contain octacalcium phosphate (OCP).

  12. Maize endophytic bacteria as mineral phosphate solubilizers.

    Science.gov (United States)

    de Abreu, C S; Figueiredo, J E F; Oliveira, C A; Dos Santos, V L; Gomes, E A; Ribeiro, V P; Barros, B A; Lana, U G P; Marriel, I E

    2017-02-16

    In the present study, we demonstrated the in vitro activity of endophytic phosphate-solubilizing bacteria (PSB). Fifty-five endophytic PSB that were isolated from sap, leaves, and roots of maize were tested for their ability to solubilize tricalcium phosphate and produce organic acid. Partial sequencing of the 16S rRNA-encoding gene showed that the isolates were from the genus Bacillus and different species of Enterobacteriaceae. The phosphate solubilization index on solid medium and phosphate solubilization in liquid medium varied significantly among the isolates. There was a statistically significant difference (P ≤ 0.05) for both, the values of phosphate-solubilizing activity and pH of the growth medium, among the isolates. Pearson correlation was statistically significant (P ≤ 0.05) between P-solubilization and pH (R = -0.38), and between the gluconic acid production and the lowering of the pH of the liquid medium at 6 (R = 0.28) and 9 days (R = 0.39). Gluconic acid production was prevalent in all the PSB studied, and Bacillus species were most efficient in solubilizing phosphate. This is the first report on the characterization of bacterial endophytes from maize and their use as potential biofertilizers. In addition, this may provide an alternative strategy for improving the phosphorus acquisition efficiency of crop plants in tropical soils.

  13. Inducing Mineral Precipitation in Groundwater by Addition of Phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Karen E. Wright; Yoshiko Fujita; Thomas Hartmann; Mark Conrad

    2011-10-01

    Induced precipitation of phosphate minerals to scavenge trace metals and radionuclides from groundwater is a potential remediation approach for contaminated aquifers. Phosphate minerals can sequester trace elements by primary mineral formation, solid solution formation and/or adsorption, and they are poorly soluble under many environmental conditions, making them attractive for long-term sustainable remediation. The success of such engineered schemes will depend on the particular mineral phases generated, their rates of formation, and their long term stability. The purpose of this study was to examine the precipitation of calcium phosphate minerals under conditions representative of a natural groundwater. Because microorganisms are present in groundwater, and because some proposed schemes for induced phosphate mineral precipitation rely on the stimulation of native groundwater populations, we also tested the effect of bacterial cells (initial densities of 105 and 107 ml-1) within the precipitation medium. We also tested the effect of a trace mixture of propionic, isovaleric, formic and butyric acids (total concentration 0.035 mM). The experiments showed that the general progression of mineral precipitation was similar under all of the conditions, with initial formation of amorphous calcium carbonate, and transformation to poorly crystalline hydroxyapatite (HAP) by the end of the week-long experiments. The presence of the bacterial cells appeared to delay precipitation, although by the end of 7 days the overall extent of precipitation was similar for all of the treatments. The stoichiometry of the final precipitates as well as results of Rietveld refinement of x-ray diffraction data indicated that the treatments including organic acids and bacterial cells resulted in increased distortion of the HAP crystal lattice, with the higher concentration of cells resulting in the greatest distortion. Uptake of Sr into the phosphate minerals was decreased in the treatments

  14. Formation of calcium phosphate mineral materialcontrolled by microemulsion

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    In order to prepare calcium phosphate-based material with nano-structure and bioactivity, natural lecithin and n-tetradecane were used as the amphipile and the oil phase respectively, along with the water phase, to form a microemulsion template. Phosphate mineralization was induced and controlled by the microemulsion. The products, characterized by scanning electronic microscopy, infrared spectroscopy and X-ray diffraction analysis, are composed of lecithin and hydroxyapatite, and possess the nano-structure of sticks, balls and three-dimensional nets connected by tubes. These results show that the microemulsion can be used to control calcium phosphate mineralization for the preparation of biomimetic mineral materials with various nano-structures.

  15. Dense and porous titanium substrates with a biomimetic calcium phosphate coating

    Energy Technology Data Exchange (ETDEWEB)

    Ribeiro, A.A., E-mail: aantunesr@yahoo.com.br [Powder Technology Laboratory, Materials Processing and Characterization Division, National Institute of Technology, No. 82 Venezuela Avenue, Room 602, 20081-312 Rio de Janeiro, RJ (Brazil); Balestra, R.M. [Powder Technology Laboratory, Materials Processing and Characterization Division, National Institute of Technology, No. 82 Venezuela Avenue, Room 602, 20081-312 Rio de Janeiro, RJ (Brazil); Rocha, M.N. [Metallurgical and Materials Engineering Program, COPPE, Federal University of Rio de Janeiro, P.O. Box 68505, 21941-972 Rio de Janeiro, RJ (Brazil); Peripolli, S.B. [Materials Metrology Division, National Institute of Metrology, Normalization and Quality, No. 50 Nossa Senhora das Gracas Street, Building 3, 25250-020 Duque de Caxias, RJ (Brazil); Andrade, M.C. [Polytechnic Institute of Rio de Janeiro, Rio de Janeiro State University, s/n, Alberto Rangel Street, 28630-050 Nova Friburgo, RJ (Brazil); Pereira, L.C. [Metallurgical and Materials Engineering Program, COPPE, Federal University of Rio de Janeiro, P.O. Box 68505, 21941-972 Rio de Janeiro, RJ (Brazil); Oliveira, M.V. [Powder Technology Laboratory, Materials Processing and Characterization Division, National Institute of Technology, No. 82 Venezuela Avenue, Room 602, 20081-312 Rio de Janeiro, RJ (Brazil)

    2013-01-15

    Highlights: Black-Right-Pointing-Pointer A biomimetic coating method with simplified solution is proposed. Black-Right-Pointing-Pointer Titanium substrates are submitted to chemical and heat treatments. Black-Right-Pointing-Pointer Titanium substrates are coated with biocompatible calcium phosphate phases. Black-Right-Pointing-Pointer The simplified solution shows potential to be applied as a coating technique. - Abstract: The present work studied a biomimetic method using a simplified solution (SS) with calcium and phosphorus ions for coating titanium substrates, in order to improve their bioactivity. Commercially pure titanium dense sheet, microporous and macroporous titanium samples, both produced by powder metallurgy, were treated in NaOH solution followed by heat-treating and immersed in SS for 7, 14 or 21 days. The samples characterization was performed by quantitative metallographic analysis, confocal scanning optical microscopy, scanning electron microscopy, energy dispersive spectroscopy and low angle X-ray diffraction. The results showed coatings with calcium phosphate precipitation in all samples, with globular or plate-like morphology, typical of hydroxyapatite and octacalcium phosphate, respectively, indicating that the solution (SS) has potential for coating titanium substrates. In addition, the different surfaces of substrates had an effect on the formed calcium phosphate phase and thickness of coatings, depending on the substrate type and imersion time in the simplified solution.

  16. Inducing mineral precipitation in groundwater by addition of phosphate

    Directory of Open Access Journals (Sweden)

    Hartmann Thomas

    2011-10-01

    Full Text Available Abstract Background Induced precipitation of phosphate minerals to scavenge trace elements from groundwater is a potential remediation approach for contaminated aquifers. The success of engineered precipitation schemes depends on the particular phases generated, their rates of formation, and their long term stability. The purpose of this study was to examine the precipitation of calcium phosphate minerals under conditions representative of a natural groundwater. Because microorganisms are present in groundwater, and because some proposed schemes for phosphate mineral precipitation rely on stimulation of native microbial populations, we also tested the effect of bacterial cells (initial densities of 105 and 107 mL-1 added to the precipitation medium. In addition, we tested the effect of a trace mixture of propionic, isovaleric, formic and butyric acids (total concentration 0.035 mM. Results The general progression of mineral precipitation was similar under all of the study conditions, with initial formation of amorphous calcium phosphate, and transformation to poorly crystalline hydroxylapatite (HAP within one week. The presence of the bacterial cells appeared to delay precipitation, although by the end of the experiments the overall extent of precipitation was similar for all treatments. The stoichiometry of the final precipitates as well as Rietveld structure refinement using x-ray diffraction data indicated that the presence of organic acids and bacterial cells resulted in an increasing a and decreasing c lattice parameter, with the higher concentration of cells resulting in the greatest distortion. Uptake of Sr into the solids was decreased in the treatments with cells and organic acids, compared to the control. Conclusions Our results suggest that the minerals formed initially during an engineered precipitation application for trace element sequestration may not be the ones that control long-term immobilization of the contaminants. In

  17. Calcium phosphate bioceramics induce mineralization modulated by proteins.

    Science.gov (United States)

    Wang, Kefeng; Leng, Yang; Lu, Xiong; Ren, Fuzeng

    2013-08-01

    Proteins play an important role in the process of biomineralization, which is considered the critical process of new bone formation. The calcium phosphate (Ca-P) mineralization happened on hydroxyapatite (HA), β-tricalcium phosphate (β-TCP) and biphasic calcium phosphate (BCP) when proteins presented were investigated systematically. The results reveal that the presence of protein in the revised simulated body fluid (RSBF) did not alter the shape and crystal structure of the precipitated micro-crystals in the Ca-P layer formed on the three types of bioceramics. However, the morphology of the Ca-P precipitates was regulated but the structure of Ca-P crystal was unchanged in vivo. The presence of proteins always inhibits Ca-P mineralization in RSBF and the degree of inhibitory effect is concentration dependent. Furthermore, Protein presence can increase the possibility of HA precipitation in vitro and in vivo. The results obtained in this study can be helpful for better understanding the mechanism of biomineralization induced by the Ca-P bioceramics.

  18. Co-precipitation of phosphate and carbonate minerals: geological and ecological implications

    Science.gov (United States)

    Sanchez-Román, Monica; McKenzie, Judith; Vasconcelos, Crisogono

    2015-04-01

    Microorganisms play an important role in natural environments by controlling the metal cations (e.g., Ca2+, Mg2+, Fe2+) and the anions (CO32-, NH4+, PO43-) that precipitate as biominerals (e.g., carbonates, phosphates). In contrast to phosphate minerals, precipitation of carbonate minerals by bacteria has been widely studied in culture experiments and in natural environments. Moreover, studies of sedimentary phosphate minerals and their geological and ecological implications are rare. Nevertheless, phosphate minerals frequently co-precipitate with carbonates in culture experiments and in natural systems. In the present work, we investigate how microorganisms control the mineralogy and geochemistry of phosphate and carbonate minerals. For this, culture experiments were performed to study the co-precipitation of phosphate and carbonate minerals using aerobic heterotrophic bacteria at sedimentary Earth's surface conditions. Ca-Mg carbonate (dolomite, Mg-calcite) and/or Mg-carbonate (hydromagnesite) precipitated with Mg-phosphate (struvite). In most of the cultures, phosphate was the dominant mineral phase found in the bacterial precipitates and carbonates precipitated after phosphate phases. Notably, in all the cultures, we found a mixture of phosphate and carbonate minerals. This study shines new light into the microbial diagenetic processes involved in the co-precipitation of phosphate and carbonate minerals and links the P and C cycles.

  19. Synthesis and characterization of nanocomposite powders of calcium phosphate/titanium oxide for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Delima, S.A.; Camargo, N.H.A.; Souza, J.C.P.; Gemelli, E., E-mail: sarahamindelima@hotmail.com, E-mail: dem2nhac@joinville.udesc.br, E-mail: souzajulio@joinville.udesc.br, E-mail: gemelli@joinville.udesc.br [Universidade do Estado de Santa Catarina (UDESC), Joinville, SC (Brazil). Centro de Ciencias Tecnologicas

    2009-07-01

    The nanostructured bioceramics of calcium phosphate are current themes of research and they are becoming important as bone matrix in regeneration of tissues in orthopedic and dental applications. Nanocomposite powders of calcium phosphate, reinforced with nanometric particles of titanium oxide, silica oxide and alumina oxid ealpha, are being widely studied because they offer new microstructures, nanostructures and interconnected microporosity with high superficial area of micropores that contribute to osteointegration and osteoinduction processes. This study is about the synthesis of nanocomposites powders of calcium phosphate reinforced with 1%, 2%, 3% and 5% in volume of titanium oxide and its characterization through the techniques of X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Differential Thermal Analysis (DTA), Thermogravimetry (TG) and Dilatometry. (author)

  20. Mineral phosphate solubilizing bacterial community in agro-ecosystem

    African Journals Online (AJOL)

    STORAGESEVER

    2009-12-15

    Dec 15, 2009 ... patterns. Four insoluble phosphate sources; purulia rock phosphate (PRP), mussourie rock phosphate .... phosphate in gradient soils, there might be changes in ..... resistance properties, fatty acid profiling and nucleic acid.

  1. Osteogenic potential of bone marrow stromal cells on smooth, roughened, and tricalcium phosphate-modified titanium alloy surfaces.

    LENUS (Irish Health Repository)

    Colombo, John S

    2012-09-01

    This study investigated the influence of smooth, roughened, and tricalcium phosphate (TCP)-coated roughened titanium-aluminum-vanadium (Ti-6Al-4V) surfaces on the osteogenic potential of rat bone marrow stromal cells (BMSCs).

  2. Functionalized titanium oxide surfaces with phosphated carboxymethyl cellulose: characterization and bonelike cell behavior.

    Science.gov (United States)

    Pasqui, Daniela; Rossi, Antonella; Di Cintio, Federica; Barbucci, Rolando

    2007-12-01

    The performance of dental or orthopedic implants is closely dependent on surface properties in terms of topography and chemistry. A phosphated carboxymethylcellulose containing one phosphate group for each disaccharide unit was synthesized and used to functionalize titanium oxide surfaces with the aim to improve osseointegration with the host tissue. The modified surfaces were chemically characterized by means of X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. The investigation of the surface topography was performed by atomic force microscopy measurements before and after the polysaccharide coating. In vitro biological tests using osteoblastlike cells demonstrated that functionalized TiO(2) surfaces modulated cell response, in terms of adhesion, proliferation,and morphology. Phosphated carboxymethylcellulose promoted better cell adhesion and significantly enhanced their proliferation. The morphology of cells was polygonal and more spread on this type of modified surface.These findings suggest that the presence of a phosphate polysaccharide coating promotes osteoblast growth on the surface potentially improving biomaterial osseointegration.

  3. Influence of pulse ratio on codeposition of copper species with calcium phosphate coatings on titanium by means of electrochemically assisted deposition.

    Science.gov (United States)

    Wolf-Brandstetter, Cornelia; Oswald, Steffen; Bierbaum, Susanne; Wiesmann, Hans-Peter; Scharnweber, Dieter

    2014-01-01

    Aim of this study was to combine the well-known biocompatibility and ostoeconductivity of thin calcium phosphate coatings on titanium with proangiogenic signals from codeposited copper species. Copper species could be integrated in mineral layers based on hydroxyapatite by means of electrochemically assisted deposition from electrolytes containing calcium, phosphate, and copper ions. Different combinations of duration and intensity of galvanostatic pulses result in different amounts of deposited calcium phosphate and of copper species even for the same applied total charge. Absolute amounts of copper varied between 2.1 and 6.9 μg/cm², and the copper was distributed homogeneously as shown by EDX mapping. The presence of copper did not change the crystalline phase of deposited calcium phosphate (hydroxyapatite) but provoked a significant decrease in deposited amounts by factor 3 to 4. The copper was deposited mainly as Cu(I) species with a minor fraction of basic copper phosphates. Reduction of copper occurred not only at the surface of titanium but also within the hydroxyapatite coating due to the reaction with hydrogen produced by the electrolysis of water during the cathodic polarization of the substrate.

  4. Calcium phosphate thin films enhance the response of human mesenchymal stem cells to nanostructured titanium surfaces

    Directory of Open Access Journals (Sweden)

    Mura M McCafferty

    2014-05-01

    Full Text Available The development of biomaterial surfaces possessing the topographical cues that can promote mesenchymal stem cell recruitment and, in particular, those capable of subsequently directing osteogenic differentiation is of increasing importance for the advancement of tissue engineering. While it is accepted that it is the interaction with specific nanoscale topography that induces mesenchymal stem cell differentiation, the potential for an attendant bioactive chemistry working in tandem with such nanoscale features to enhance this effect has not been considered to any great extent. This article presents a study of mesenchymal stem cell response to conformal bioactive calcium phosphate thin films sputter deposited onto a polycrystalline titanium nanostructured surface with proven capability to directly induce osteogenic differentiation in human bone marrow–derived mesenchymal stem cells. The sputter deposited surfaces supported high levels of human bone marrow–derived mesenchymal stem cell adherence and proliferation, as determined by DNA quantification. Furthermore, they were also found to be capable of directly promoting significant levels of osteogenic differentiation. Specifically, alkaline phosphatase activity, gene expression and immunocytochemical localisation of key osteogenic markers revealed that the nanostructured titanium surfaces and the bioactive calcium phosphate coatings could direct the differentiation towards an osteogenic lineage. Moreover, the addition of the calcium phosphate chemistry to the topographical profile of the titanium was found to induce increased human bone marrow–derived mesenchymal stem cell differentiation compared to that observed for either the titanium or calcium phosphate coating without an underlying nanostructure. Hence, the results presented here highlight that a clear benefit can be achieved from a surface engineering strategy that combines a defined surface topography with an attendant, conformal

  5. Synthesis and Electrochemical Performance of a Lithium Titanium Phosphate Anode for Aqueous Lithium-Ion Batteries

    KAUST Repository

    Wessells, Colin

    2011-01-01

    Lithium-ion batteries that use aqueous electrolytes offer safety and cost advantages when compared to today\\'s commercial cells that use organic electrolytes. The equilibrium reaction potential of lithium titanium phosphate is -0.5 V with respect to the standard hydrogen electrode, which makes this material attractive for use as a negative electrode in aqueous electrolytes. This material was synthesized using a Pechini type method. Galvanostatic cycling of the resulting lithium titanium phosphate showed an initial discharge capacity of 115 mAh/g and quite good capacity retention during cycling, 84% after 100 cycles, and 70% after 160 cycles at a 1 C cycling rate in an organic electrolyte. An initial discharge capacity of 113 mAh/g and capacity retention of 89% after 100 cycles with a coulombic efficiency above 98% was observed at a C/5 rate in pH -neutral 2 M Li2 S O4. The good cycle life and high efficiency in an aqueous electrolyte demonstrate that lithium titanium phosphate is an excellent candidate negative electrode material for use in aqueous lithium-ion batteries. © 2011 The Electrochemical Society.

  6. Titanium minerals of placer deposits as a source for new materials

    Science.gov (United States)

    Kotova, Olga; Ponaryadov, Alexey

    2015-04-01

    Heavy mineral deposits are a source of the economic important element titanium, which is contained in ilmenite and leucoxene. The mineral composition of placer titanium ore and localization pattern of ore minerals determine their processing and enriching technologies. New data on the mineralogy of titanium ores from modern coastal-marine placer in Stradbroke Island, Eastern Australia, and Pizhma paleoplacer in Middle Timan, Russia, and materials on their basis are presented. The samples were studied by the following methods: optical-mineralogical (stereomicroscope MBS-10, polarizing microscope POLAM L-311), semiquantitative x-ray phase analysis (x-ray difractometer X'Pert PRO MPD). Besides microprobe (VEGA 3 TESCAN) and x-ray fluorescent analysis (XRF-1800 Shimadzu) were used. By the mineralogical composition ores of the both deposits are complex: enriched by valuable minerals. Apart from main ore concentrates it is possible to obtain accompanying nonmetallic products. This will increase the efficiency of deposit exploitation. Ilmenite dominates in ore sands of Stradbroke Island, and leucoxene dominates in the ores of the Pizhma titanium deposit. Australian ilmenite and its altered varieties are mainly characterized by a very high MnO content (from 5.24 to 11.08 %). The irregular distribution of iron oxides, titanium and manganese in the altered ilmenite was shown in the paper. E.g., in the areas of substitution of ilmenite by pseudorutile the concentrations of the given elements are greatly various due to various ratios of basic components in each grain. Their ratios are equal in the area of rutile evolution. Moreover, the high content of gold, diamonds and also rare earth elements (REE) and rare metals (their forms are not determined) were studied. We found native copper on the surface of minerals composing titanium-bearing sandstones of the Pizhma placer. According to the technological features of rocks (density and magnetic) studied placers are close. The

  7. Laser processing of bioactive tricalcium phosphate coating on titanium for load-bearing implants.

    Science.gov (United States)

    Roy, Mangal; Vamsi Krishna, B; Bandyopadhyay, Amit; Bose, Susmita

    2008-03-01

    Laser-engineered net shaping (LENS), a commercial rapid prototyping (RP) process, was used to coat titanium with tricalcium phosphate (TCP) ceramics to improve bone cell-materials interactions. During LENS coating process, the Nd:YAG laser melts the top surface of Ti substrate in which calcium phosphate powder is fed to create a TCP-Ti composite layer. It was found that an increase in laser power and/or powder feed rate increases the thickness of the coating. However, coating thickness decreased with increasing laser scan speed. TCP coating showed columnar titanium grains at the substrate side of the coating and transitioned to equiaxed titanium grains at the outside. When the scan speed was reduced from 15 to 10mms(-1), coating hardness increased from 882+/-67 to 1049+/-112Hv due to an increase in the volume fraction of TCP in the coating. Coated surfaces showed uniformly distributed TCP particles and X-ray diffraction data confirmed the absence of any undesirable phases, while maintaining a high level of crystallinity. The effect of TCP coating on cell-material interaction was examined by culturing osteoprecursor cells (OPC1) on coated surfaces. The results indicated that TCP coating had good biocompatibility where OPC1 cells attached and proliferated on the coating surface. The coating also initiated cell differentiation, ECM formation and biomineralization.

  8. Increasing the electrochemical activity of transition metal phosphates in lithium cells by treatment with intimate carbon: The case of titanium phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Santos-Pena, J. [Departament de Quimica, Universitat de les Illes Balears, Cra. de Valldemossa, E07123 Palma de Mallorca (Spain); Soudan, P. [Laboratoire d' Electrochimie, Catalyse et Synthese Organique, UMR CNRS 7582, ISCSA, 94320 Thiais (France); Cruz-Yusta, M. [Laboratorio de Quimica Inorganica, Edificio Marie Curie, Universidad de Cordoba, E14071 Cordoba (Spain); Franger, S. [Laboratoire de Physico-Chimie de l' Etat Solide, UMR CNRS 8648, ICMMO, Universite Paris XI, 91405 Orsay (France)

    2006-06-15

    Amorphous sodium-containing titanium phosphate (sample TiP), obtained by heating a disordered precursor at 300{sup o}C under air, electrochemically reacts with lithium by means of non-aqueous lithium cells. Discharge curves of EC/DEC cells in the 3.5-1.5V region, were different to that observed for NASICON titanium phosphates but the related capacity can be associated to the reduction of Ti{sup 4+} to Ti{sup 3+}. Another sample, C-TiP, obtained by using nitrogen atmosphere during the thermal treatment, was able to provide 75% more capacity in this region. This sample contained carbon because of the incomplete pyrolysis of the surfactant present in the precursor. Carbon is supposed to stay occluded inside the pores considering the values of pores surface area, total conductivity and HRTEM measurements. These titanium phosphates were also tested as negative electrodes. Electrochemical impedance spectroscopy measurements suggest that both titanium phosphates are reduced to yield titanium, lithia and phosphorus at 0.0V. In our opinion, the presence of carbon in C-TiP is the key factor for the enhanced reactivity in the 3.2-1.5V region but is not enough to obtain a good electrochemical performance, in terms of cycling efficiency. (author)

  9. Electrochemically assisted deposition of strontium modified magnesium phosphate on titanium surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Meininger, M. [Department for Functional Materials in Medicine and Dentistry, University of Würzburg, Pleicherwall 2, D-97070 Würzburg (Germany); Wolf-Brandstetter, C. [Max Bergmann Center for Biomaterials, Technical University of Dresden, Budapester Straße 27, D-01069 Dresden (Germany); Zerweck, J.; Wenninger, F.; Gbureck, U.; Groll, J. [Department for Functional Materials in Medicine and Dentistry, University of Würzburg, Pleicherwall 2, D-97070 Würzburg (Germany); Moseke, C., E-mail: claus.moseke@fmz.uni-wuerzburg.de [Department for Functional Materials in Medicine and Dentistry, University of Würzburg, Pleicherwall 2, D-97070 Würzburg (Germany)

    2016-10-01

    Electrochemically assisted deposition was utilized to produce ceramic coatings on the basis of magnesium ammonium phosphate (struvite) on corundum-blasted titanium surfaces. By the addition of defined concentrations of strontium nitrate to the coating electrolyte Sr{sup 2+} ions were successfully incorporated into the struvite matrix. By variation of deposition parameters it was possible to fabricate coatings with different kinetics of Sr{sup 2+} into physiological media, whereas the release of therapeutically relevant strontium doses could be sustained over several weeks. Morphological and crystallographic examinations of the immersed coatings revealed that the degradation of struvite and the release of Sr{sup 2+} ions were accompanied by a transformation of the coating to a calcium phosphate based phase similar to low-crystalline hydroxyapatite. These findings showed that strontium doped struvite coatings may provide a promising degradable coating system for the local application of strontium or other biologically active metal ions in the implant–bone interface. - Highlights: • Sr-doped struvite coatings have been deposited on titanium by electrochemically assisted deposition. • Sr content can be adjusted by means of process time, current density and pulse mode. • Sr-doped coatings release therapeutically relevant Sr doses in physiological media for several weeks. • During immersion in physiological media Sr-doped struvite coatings transform into a low crystalline calcium phosphate phase.

  10. Structural modification of titanium surface by octacalcium phosphate via Pulsed Laser Deposition and chemical treatment

    Directory of Open Access Journals (Sweden)

    I.V. Smirnov

    2017-06-01

    Full Text Available In the present study, the Pulsed Laser Deposition (PLD technique was applied to coat titanium for orthopaedic and dental implant applications. Calcium carbonate (CC was used as starting coating material. The deposited CC films were transformed into octacalcium phosphate (OCP by chemical treatments. The results of X-ray diffraction (XRD, Raman, Fourier Transform Infrared Spectroscopy (FTIR and scanning electron microscopy (SEM studies revealed that the final OCP thin films are formed on the titanium surface. Human myofibroblasts from peripheral vessels and the primary bone marrow mesenchymal stromal cells (BMMSs were cultured on the investigated materials. It was shown that all the investigated samples had no short-term toxic effects on cells. The rate of division of myofibroblast cells growing on the surface and saturated BMMSs concentration for the OCP coating were about two times faster than of cells growing on the CC films.

  11. A New Organo-Directed Titanium Phosphate Phase Containing Zigzag Chains of Corner-Sharing TiO6 Octahedra

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    A new organo-directed titanium phosphate, [NH3CH2CH2NH3]·[TiO(HPO4)2], was synthesized by the solvothermal method and its structure was determined by single crystal X-ray diffraction. The structure consists of 1-D zigzag chains built up from trans-corner-sharing titanium oxo octahedra running along the b axis, with fused Ti2P three-membered rings being attached to the - Ti - O - Ti - O - backbone.

  12. New developments in polymer-controlled, bioinspired calcium phosphate mineralization from aqueous solution.

    Science.gov (United States)

    Bleek, Katrin; Taubert, Andreas

    2013-05-01

    The polymer-controlled and bioinspired precipitation of inorganic minerals from aqueous solution at near-ambient or physiological conditions avoiding high temperatures or organic solvents is a key research area in materials science. Polymer-controlled mineralization has been studied as a model for biomineralization and for the synthesis of (bioinspired and biocompatible) hybrid materials for a virtually unlimited number of applications. Calcium phosphate mineralization is of particular interest for bone and dental repair. Numerous studies have therefore addressed the mineralization of calcium phosphate using a wide variety of low- and high-molecular-weight additives. In spite of the growing interest and increasing number of experimental and theoretical data, the mechanisms of polymer-controlled calcium phosphate mineralization are not entirely clear to date, although the field has made significant progress in the last years. A set of elegant experiments and calculations has shed light on some details of mineral formation, but it is currently not possible to preprogram a mineralization reaction to yield a desired product for a specific application. The current article therefore summarizes and discusses the influence of (macro)molecular entities such as polymers, peptides, proteins and gels on biomimetic calcium phosphate mineralization from aqueous solution. It focuses on strategies to tune the kinetics, morphologies, final dimensions and crystal phases of calcium phosphate, as well as on mechanistic considerations.

  13. Mesoporous titanium phosphates and related molecular sieves: Synthesis, characterization and applications

    Indian Academy of Sciences (India)

    Asim Bhaumik

    2002-08-01

    Titanium (IV) phosphates TCM-7 and -8 with mesoporous cationic framework topologies using both cationic and anionic surfactants have been synthesized. Experimental data suggest the stabilization of the tetrahedral state of Ti in TCM-7/8 (O-P-O-Ti-O-, at Ti/P = 1:1) vis-à-vis the most stable octahedral state of Ti in the rutile/anatase or pure mesoporous TiO2. Mesoporous TCM-7 and -8 show anion exchange capacity due to the framework phosphonium cation and cation exchange capacity due to defective P-OH groups. Grafting the organic functionality in the surface or bridging the organic moiety in between the inorganic phosphorus precursors can enhance hydrophobicity of these materials similar to that of mesoporous silica materials. The high catalytic activity in the liquid phase partial oxidation of cyclohexene over such organically surface modified mesoporous titanium phosphate using a dilute H2O2 oxidant supports the tetrahedral coordination of Ti in these materials. These materials also show excellent photocatalytic activity in the production of H2 by photo-reduction of water under UV light irradiation.

  14. Titanium mineralization in ferritin: a room temperature nonphotochemical preparation and biophysical characterization.

    Science.gov (United States)

    Amos, Fairland F; Cole, Kathryn E; Meserole, Rachel L; Gaffney, Jean P; Valentine, Ann M

    2013-01-01

    The incremental addition of titanium(III) citrate to H-chain homopolymers of human ferritin results in the formation of 1.5-6.5-nm particles of amorphous TiO(2) within the nanocage of the protein. The mineralization conditions are mild, featuring ambient temperature and no need for photochemical activation. Low ratios of titanium to protein favor intraprotein mineralization, and the products are characterized by stained and unstained transmission electron microscopy, UV-vis spectroscopy, dynamic light scattering, analytical ultracentrifugation, and metal analysis. With up to 1,000 equiv of metal, there is no change to the protein hydrodynamic radius or diffusion constant. There is, however, a systematic shift in the sedimentation coefficient, which confirms mineralization within the protein core.

  15. Scientific basis for creation of construction materials based on titanium and alumina minerals

    Science.gov (United States)

    Kotova, O.; Shmakova, A.; Ponaryadov, A.

    2017-02-01

    Currently there is a need in affordable and accessible materials with specific physical and chemical properties. Al- and Ti-minerals are excellent test objects for correlation between structure and physical properties of mineral. For example, corundum and ilmenite are related to the same structural type (rhombohedral lattice R3) and possess various physical properties. With the help of modern equipment we studied titanium- and aluminum-containing concentrates of natural raw and also products of various kinds of influences on them, which showed signs of nanostructuring. We observed methods of directional change of physical and chemical characteristics of Al- and Ti-minerals and creation of new commercial products.

  16. In vitro and in vivo degradation of biomimetic octacalcium phosphate and carbonate apatite coatings on titanium implants

    NARCIS (Netherlands)

    Barrere, F.; Valk, van der C.M.; Dalmeijer, R.A.J.; Blitterswijk, van C.A.; Groot, de K.; Layrolle, P.

    2003-01-01

    Calcium phosphate (Ca-P) coatings have been applied onto titanium alloys prosthesis to combine the srength of metals with the bioactivity of Ca-P. It has been clearly shown in many publications that Ca-P coating accelerates bone formation around the implant. However, longevity of the Ca-P coating fo

  17. Characterization of the mineral phosphate solubilizing activity of Serratia marcescens CTM 50650 isolated from the phosphate mine of Gafsa.

    Science.gov (United States)

    Ben Farhat, Mounira; Farhat, Ameny; Bejar, Wacim; Kammoun, Radhouan; Bouchaala, Kameleddine; Fourati, Amin; Antoun, Hani; Bejar, Samir; Chouayekh, Hichem

    2009-11-01

    The mineral phosphate solubilizing (MPS) ability of a Serratia marcescens strain, namely CTM 50650, isolated from the phosphate mine of Gafsa, was characterized on a chemically defined medium (NBRIP broth). Various insoluble inorganic phosphates, including rock phosphate (RP), calcium phosphate (CaHPO(4)), tri-calcium phosphate (Ca(3)(PO(4))(2)) and hydroxyapatite were tested as sole sources of phosphate for bacterial growth. Solubilization of these phosphates by S. marcescens CTM 50650 was very efficient. Indeed, under optimal conditions, the soluble phosphorus (P) concentration it produced reached 967, 500, 595 and 326 mg/l from CaHPO(4), Ca(3)(PO(4))(2), hydroxyapatite and RP, respectively. Study of the mechanisms involved in the MPS activity of CTM 50650, showed that phosphate solubilization was concomitant with significant drop in pH. HPLC-analysis of culture supernatants revealed the secretion of gluconic acid (GA) resulting from direct oxidation pathway of glucose when the CTM 50650 cells were grown on NBRIP containing glucose as unique carbon source. This was correlated with the simultaneous detection by PCR for the first time in a S. marcescens strain producing GA, of a gene encoding glucose dehydrogenase responsible for GA production, as well as the genes pqqA, B, C and E involved in biosynthesis of its PQQ cofactor. This study is expected to lead to the development of an environmental-friendly process for fertilizer production considering the capacity of S. marcescens CTM 50650 to achieve yields of P extraction up to 75% from the Gafsa RP.

  18. Raman and infrared spectroscopic characterization of beryllonite, a sodium and beryllium phosphate mineral - implications for mineral collectors.

    Science.gov (United States)

    Frost, Ray L; Xi, Yunfei; Scholz, Ricardo; Belotti, Fernanda M; Alberto Dias Menezes Filho, Luiz

    2012-11-01

    The mineral beryllonite has been characterized by the combination of Raman spectroscopy and infrared spectroscopy. SEM-EDX was used for the chemical analysis of the mineral. The intense sharp Raman band at 1011 cm(-1), was assigned to the phosphate symmetric stretching mode. Raman bands at 1046, 1053, 1068 and the low intensity bands at 1147, 1160 and 1175 cm(-1) are attributed to the phosphate antisymmetric stretching vibrations. The number of bands in the antisymmetric stretching region supports the concept of symmetry reduction of the phosphate anion in the beryllonite structure. This concept is supported by the number of bands found in the out-of-plane bending region. Multiple bands are also found in the in-plane bending region with Raman bands at 399, 418, 431 and 466 cm(-1). Strong Raman bands at 304 and 354 cm(-1) are attributed to metal oxygen vibrations. Vibrational spectroscopy served to determine the molecular structure of the mineral. The pegmatitic phosphate minerals such as beryllonite are more readily studied by Raman spectroscopy than infrared spectroscopy. Copyright © 2012 Elsevier B.V. All rights reserved.

  19. Chromatographic separation of inorganic ions on thin layers of titanium phosphate ion-exchanger.

    Science.gov (United States)

    Ghoulipour, Vanik; Safari, Moharram

    2014-12-01

    The chromatographic behavior of 30 inorganic cations has been studied on thin layers of titanium phosphate ion-exchanger using several aqueous, organic and mixed mobile phases. The separation of one ion from several other ions and also ternary and binary separations have been developed. Some important analytical separations are reported. The effect of pH of the mobile phase on retention factor (Rf) values of the cations in the presence of complex-forming anion along with the separation power of the ion-exchanger were studied. This ion-exchanger exhibits high sorption capacity and varying selectivity towards metal ions and makes it a suitable stationaiy phase in thin layer chromatography.

  20. Chromatographic separation of inorganic ions on thin layers of titanium phosphate ion-exchanger

    Institute of Scientific and Technical Information of China (English)

    Vanik GHOULIPOUR; Moharram SAFARI

    2014-01-01

    The chromatographic behavior of 30 inorganic cations has been studied on thin layers of titanium phosphate ion-exchanger using several aqueous,organic and mixed mobile phases. The separation of one ion from several other ions and also ternary and binary separations have been developed. Some important analytical separations are reported. The effect of pH of the mobile phase on retention factor(Rf)values of the cations in the presence of complex-forming anion along with the separation power of the ion-exchanger were studied. This ion-exchanger exhibits high sorption capacity and varying selectivity towards metal ions and makes it a suitable stationary phase in thin layer chromatography.

  1. Ammonia vapor sensing properties of polyaniline-titanium(IV)phosphate cation exchange nanocomposite.

    Science.gov (United States)

    Khan, Asif Ali; Baig, Umair; Khalid, Mohd

    2011-02-28

    In this study, the electrically conducting polyaniline-titanium(IV)phosphate (PANI-TiP) cation exchange nanocomposite was synthesized by sol-gel method. The cation exchange nanocomposite based sensor for detection of ammonia vapors was developed at room temperature. It was revealed that the sensor showed good reversible response towards ammonia vapors ranging from 3 to 6%. It was found that the sensor with p-toluene sulphonic acid (p-TSA) doped exhibited higher sensing response than hydrochloric acid doped. This sensor has detection limit ≤1% ammonia. The response of resistivity changes of the cation exchange nanocomposite on exposure to different concentrations of ammonia vapors shows its utility as a sensing material. These studies suggest that the cation exchange nanocomposite could be a good material for ammonia sensor at room temperature.

  2. Analysis of sugar phosphates in plants by ion chromatography on a titanium dioxide column with pulsed amperometric detection.

    Science.gov (United States)

    Sekiguchi, Yoko; Mitsuhashi, Naoto; Inoue, Yoshinori; Yagisawa, Hitoshi; Mimura, Tetsuro

    2004-06-11

    This paper describes the development of a practical method for the analysis of sugar phosphates from the model higher plant Arabidopsis thaliana by high-performance anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD). The extraction method of sugar phosphates from higher plants was first optimized for HPAEC-PAD analysis. In order to improve the resolution in HPAEC-PAD, a column packed with titanium dioxide resin was used. The titanium dioxide column was used as a trap-column for sugar phosphates and nucleotides, for the removal of sample matrices. Sample pretreatment was achieved in-line and automatically using a six-port valve placed after the injection valve.

  3. Synthesis, characterization, antimicrobial and cytotoxicity studies of a novel titanium dodecylamino phosphate

    Directory of Open Access Journals (Sweden)

    A. Rajini

    2017-01-01

    Full Text Available A novel titanium dodecylamino phosphate has been synthesized instantly at ambient temperature and characterized by various analytical and spectroscopic techniques such as PXRD, SEM-EDAX, TGA/DTA, FT-IR, dispersive Raman, UV–Vis DRS, XPS, 31P and 13C MAS NMR. The material was tested for biological activities such as antimicrobial, nematicidal and anticancer. The material exhibits potent antimicrobial activity against Gram-positive bacteria and fungi. The percentage mortality against Meloidogyne incognita nematode was increased with increase in concentration and incubation time. Further the material was also investigated for anticancer on human cancer cell lines such as cervix (HeLa, leukemia (HL60 and breast (MCF7. The cells were dosed with varying concentrations of the material and cell viability was measured by sulforhodamine-B (SRB calorimetric assay. Interestingly, the material shows GI50 values of 39.8 μg mL−1 (HL60, 13.2 μg mL−1 (MCF7 and a superior value of 10.6 μg mL−1 (HeLa, respectively. However the material was found to be excellent and active against HeLa and MCF7 than HL60 cells leading to the conclusion that presence of titanium and amino groups were responsible for cytotoxicity.

  4. Microbial mineralization of struvite: a promising process to overcome phosphate sequestering crisis.

    Science.gov (United States)

    Sinha, Arvind; Singh, Amit; Kumar, Sumit; Khare, Sunil Kumar; Ramanan, Arunachalam

    2014-05-01

    Due to extensive exploitation of non-renewable phosphate minerals, their natural reserves will exhaust very soon. This necessitates looking for alternatives and an efficient methodology through which indispensable phosphorus can be harvested back. The current study was undertaken to explore the potential of a metallophilic bacterium Enterobacter sp. EMB19 for the recovery of phosphorus as phosphate rich mineral. A very low phosphate concentration strategy was adopted. The process led to the mineralization of phosphorus as homogeneous struvite crystals. For each gram of Epsom salt added, the cells effectively mineralized about 20% of the salt into struvite. The effect of different inorganic sources, culture profile and plausible mechanism involved in crystal formation was also explored. The synthesized struvite crystals typically possessed a prismatic crystal habit. The characterization and identification of the crystals were done using single crystal X-ray diffraction (SCXRD), powder X-ray diffraction (PXRD), energy dispersive X-ray analysis (EDAX) and fourier transform infrared (FTIR). The thermal characteristics were studied using thermo gravimetric analysis (TGA) and differential scanning calorimetric (DSC) processes. The synthesis of struvite by this bacterium seems to be a promising and viable strategy since it serves dual purpose (i) obtaining phosphorus and nitrogen rich fertilizer and (ii) conservation of natural phosphate reserves. This study is very significant in the sense that the process may be used for harvesting and synthesizing other valuable minerals. Also, it will provide new insights into phosphate biomineralization mechanisms.

  5. A cryogenic fluorescence spectroscopic study of uranyl carbonate, phosphate, and oxyhydroxide minerals

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Zheming; Zachara, John M.; Liu, Chongxuan; Gassman, Paul L.; Felmy, Andrew R.; Clark, Sue B.

    2008-11-03

    In this work we have applied liquid-helium temperature (LHeT) time-resolved laser-induced fluorescence spectroscopy (TRLIF) to characterize a series of natural and synthetic minerals of uranium carbonate, phosphate and oxyhydroxides including rutherfordine, zellerite, liebigite, phosphuranylite, meta-autunite, meta-torbernite, uranyl phosphate, sodium-uranyl-phosphate, bequerelite, clarkeite, curite, schoepite and compregnacite, and compared their spectral characteristics among these minerals as well as our previously published data on uranyl silicates. For the carbonate minerals, the fluorescence spectra depend on the stoichiometry of the mineral. For the phosphate minerals the fluorescence spectra closely resemble each other despite the differences in their composition and structure. For all uranium oxyhydroxides, the fluorescence spectra are largely red-shifted as compared with those of the uranium carbonates and phosphates and their vibronic bands are broadened and less resolved. The much enhanced spectra resolution at LHeT allows more accurate calculation of the O=U=O symmetrical stretch frequency, ν1, corresponding to the average spacing of the vibronic peaks of the fluorescence spectra and the spectral origin as reflected by the position of the first vibronic band. It was found that both the average ν1 and λ1 values correlate well with the average basicity of the inorganic anion.

  6. Effect Of Gravity On Porous Tricalcium Phosphate And Nonstoichiometric Titanium Carbide Produced Via Combustion Synthesis

    Science.gov (United States)

    Castillo, M.; Moore, J. J.; Schowengerdt, F. D.; Ayers, R. A.

    2003-01-01

    Novel processing techniques, such as self-propagating high temperature synthesis (SHS), have the capability to rapidly produce advanced porous materials that are difficult to fabricate by other methods. This processing technique is also capable of near net shape synthesis, while variable gravity allows the manipulation of the structure and composition of the material. The creation of porous tricalcium phosphate (TCP) is advantageous in the biomaterials field, since it is both a biocompatible material and an osteoconductive material. Porous tricalcium phosphate produced via SHS is an excellent candidate for bone scaffold material in the bone regeneration process. The porosity allows for great vascularization and ingrowth of tissue. Titanium Carbide is a nonstoichiometric biocompatible material that can be incorporated into a TiC-Ti composite system using combustion synthesis. The TiC-Ti composite exhibits a wide range of mechanical and chemical properties. Both of these material systems (TCP and TiC-Ti) can be used to advantage in designing novel bone replacement materials. Gravity plays an important role in both the pore structure and the chemical uniformity of these composite systems and offers considerable potential in advanced bone engineering.

  7. Structural studies of calcium phosphate doped with titanium and zirconium obtained by high-energy mechanical alloying

    Energy Technology Data Exchange (ETDEWEB)

    Silva, C C; Sombra, A S B [Telecommunications and Materials Science and Engineering Laboratory (LOCEM), Physics Department, Federal University of Ceara, Campus do Pii, Postal Code 6030, 60455-760, Fortaleza-Ceara (Brazil)], E-mail: sombra@fisica.ufc.br

    2009-12-15

    In this paper, we present a new variation of the solid-state procedure on the synthesis of bioceramics with titanium (CapTi) and zirconium (CapZr), considering that zirconium (ZrO{sub 2}) and titanium oxide (TiO{sub 2}) are strengthening agents, due to their superb force and fracture toughness. The high efficiency of the calcination process opens a new way of producing commercial amounts of nanocrystalline bioceramics. In this work, a new variation of the solid-state procedure method was used to produce nanocrystalline powders of titanium and zirconium, using two different experimental chemical routes: CapTi: Ca(H{sub 2}PO{sub 4}){sub 2}+TiO{sub 2} and CapZr: Ca(H{sub 2}PO{sub 4}){sub 2}+ZrO{sub 2}. The powders were submitted to calcination processes (CapTic and CapZrc) at 800, 900 and 1000 deg. C. The calcium titanium phosphate phase, CaTi{sub 4}P{sub 6}O{sub 24}, was obtained in the CapTic reaction and the calcium zirconium phosphate, CaZr{sub 4}P{sub 6}O{sub 24}, was obtained in the CapZrc reaction. The obtained ceramics were characterized by x-ray powder diffraction (XRD), infrared (IR) spectroscopy, Raman scattering spectroscopy (RSS) and scanning electron microscopy (SEM) analysis. This method was compared with the milling process (CapTim and CapZrm), where in the last process the melting is not necessary and the powder obtained is nanocrystalline. The calcium titanium phosphate phase, CaTi{sub 4}P{sub 6}O{sub 24}, was obtained in the reaction CapTim, but in CapZrm the formation of any calcium phosphate phase even after 15 h of dry mechanical alloying was not observed.

  8. Structural studies of calcium phosphate doped with titanium and zirconium obtained by high-energy mechanical alloying

    Science.gov (United States)

    Silva, C. C.; Sombra, A. S. B.

    2009-12-01

    In this paper, we present a new variation of the solid-state procedure on the synthesis of bioceramics with titanium (CapTi) and zirconium (CapZr), considering that zirconium (ZrO2) and titanium oxide (TiO2) are strengthening agents, due to their superb force and fracture toughness. The high efficiency of the calcination process opens a new way of producing commercial amounts of nanocrystalline bioceramics. In this work, a new variation of the solid-state procedure method was used to produce nanocrystalline powders of titanium and zirconium, using two different experimental chemical routes: CapTi: Ca(H2PO4)2+TiO2 and CapZr: Ca(H2PO4)2+ZrO2. The powders were submitted to calcination processes (CapTic and CapZrc) at 800, 900 and 1000 °C. The calcium titanium phosphate phase, CaTi4P6O24, was obtained in the CapTic reaction and the calcium zirconium phosphate, CaZr4P6O24, was obtained in the CapZrc reaction. The obtained ceramics were characterized by x-ray powder diffraction (XRD), infrared (IR) spectroscopy, Raman scattering spectroscopy (RSS) and scanning electron microscopy (SEM) analysis. This method was compared with the milling process (CapTim and CapZrm), where in the last process the melting is not necessary and the powder obtained is nanocrystalline. The calcium titanium phosphate phase, CaTi4P6O24, was obtained in the reaction CapTim, but in CapZrm the formation of any calcium phosphate phase even after 15 h of dry mechanical alloying was not observed.

  9. Iron titanium phosphates as high-specific-capacity electrode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Essehli, R., E-mail: essehli.rachid@yahoo.fr [Laboratory of Mineral Solid and Analytical Chemistry (LMSAC), Department of Chemistry, Faculty of Sciences, University Mohamed I, PO. Box 717, 60000 Oujda (Morocco); ESECO SYSTEMS 270 rue Thomas Edison, Atelier Relais No 6, 34400 Lunel (France); El Bali, B. [Laboratory of Mineral Solid and Analytical Chemistry (LMSAC), Department of Chemistry, Faculty of Sciences, University Mohamed I, PO. Box 717, 60000 Oujda (Morocco); Faik, A. [CIC energigune, Parque Tecnológico de Álava, Albert Einstein 48, 01510 Miñano, Álava (Spain); Naji, M. [CNRS, UPR3079 CEMHTI, 1D avenue de la Recherche Scientifique, 45071 Orléans cedex 2 (France); Benmokhtar, S. [LCPGM, Laboratoire de Chimie-Physique Générale des Matériaux, Département de Chimie, Université Hassan II-Mohammedia, Faculté des Sciences Ben M’Sik, Casablanca (Morocco); Zhong, Y.R.; Su, L.W.; Zhou, Z. [Institute of New Energy Material Chemistry, Synergetic Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin 300071 (China); Kim, J.; Kang, K. [Department of Materials Science and Engineering, Seoul National University, Gwanak-ro, Gwanak-gu, Seoul 151-742 (Korea, Republic of); Dusek, M. [Institute of Physics of the ASCR, v.v.i., Na Slovance 2, 182 21 Praha 8 (Czech Republic)

    2014-02-05

    Highlights: • Iron Titanium Phosphates as High-Specific-Capacity. • Electrode Materials for Lithium ion Batteries. • During the following cycles, good reversible capacity retention and better cyclabilit. • Ex-situ XRD analysis during the first discharge shows an amorphization of this anode material. -- Abstract: Two iron titanium phosphates, Fe{sub 0.5}TiOPO{sub 4} and Fe{sub 0.5}Ti{sub 2}(PO{sub 4}){sub 3}, were prepared, and their crystal structures and electrochemical performances were compared. The electrochemical measurements of Fe{sub 0.5}TiOPO{sub 4} as an anode of a lithium ion cell showed that upon the first discharge down to 0.5 V, the cell delivered a capacity of 560 mA h/g, corresponding to the insertion of 5 Li’s per formula unit Fe{sub 0.5}TiOPO{sub 4}. Ex-situ XRD reveals a gradual evolution of the structure during cycling of the material, with lower crystallinity after the first discharge cycle. By correlating the electrochemical performances with the structural studies, new insights are achieved into the electrochemical behaviour of the Fe{sub 0.5}TiOPO{sub 4} anode material, suggesting a combination of intercalation and conversion reactions. The Nasicon-type Fe{sub 0.5}Ti{sub 2}(PO{sub 4}){sub 3} consists of a three-dimensional network made of corners and edges sharing [TiO{sub 6}] and [FeO{sub 6}] octahedra and [PO{sub 4}] tetrahedra leading to the formation of trimmers [FeTi{sub 2}O{sub 12}]. The first discharge of lithium ion cells based on Fe{sub 0.5}Ti{sub 2}(PO{sub 4}){sub 3} materials showed electrochemical activity of Ti{sup 4+}/Ti{sup 3+} and Fe{sup 2+}/Fe{sup 0} couples in the 2.5–1 V region. Below this voltage, the discharge profiles are typical of phosphate systems where Li{sub 3}PO{sub 4} is a product of the electrochemical reaction with lithium; moreover, the electrolyte solvent is reduced. An initial capacities as high as 1100 mA h g{sup −1} can be obtained at deep discharge. However, there is an irreversible capacity

  10. A cryogenic fluorescence spectroscopic study of uranyl carbonate, phosphate and oxyhydroxide minerals

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Z.; Zachara, J.M.; Liu, C.; Gassman, P.L.; Felmy, A.R. [Pacific Northwest National Lab., Richland, WA (United States); Clark, S.B. [Washington State Univ., Pullman, WA (United States)

    2008-07-01

    In this work we applied time-resolved laser-induced fluorescence spectroscopy (TRLIF) at both room temperature (RT) and near liquid-helium temperature (6 K) to characterize a series of natural and synthetic minerals of uranium carbonate, phosphate and oxyhydroxides including rutherfordine, zellerite, liebigite, phosphuranylite, meta-autunite, meta-torbernite, uranyl phosphate, sodium-uranyl-phosphate, becquerelite, schoepite, meta-schoepite, dehydrated schoepite and compreignacite, and have compared the spectral characteristics among these minerals as well as our previously published data on uranyl silicates. For the carbonate minerals, the fluorescence spectra of rutherfordine showed significant difference from those of zellerite and liebigite. The fluorescence spectra of the phosphate minerals closely resemble each other despite the differences in their composition and structure. For all uranium oxyhydroxides, the fluorescence spectra are largely red-shifted as compared to those of the uranium carbonates and phosphates and their vibronic bands are broad and less resolved at RT. The enhanced spectra resolution at 6 K allows more accurate determination of the fluorescence band origin and offers a complemental method to measure the O=U=O symmetrical stretch frequency, {nu}{sub 1}, from the spacings of the vibronic bands of the fluorescence spectra. The average {nu}{sub 1} values appear to be inversely correlated with the average pK{sub a} values of the anions. (orig.)

  11. Highly efficient solid-phase derivatization of sugar phosphates with titanium-immobilized hydrophilic polydopamine-coated silica.

    Science.gov (United States)

    Qin, Qian; Wang, Bohong; Chang, Mengmeng; Zhou, Zhihui; Shi, Xianzhe; Xu, Guowang

    2016-07-29

    Sugar phosphates are a type of key metabolic intermediates of glycolysis, gluconeogenesis and pentose phosphate pathway, which can regulate tumor energetic metabolism. Due to their low endogenous concentrations, poor chromatographic retention properties as well as ionization suppression from complex matrix interference, the determination of sugar phosphates in biological samples is very difficult. In this study, titanium-immobilized hydrophilic polydopamine-coated silica microspheres (SiO2@PD-Ti(4+)) were synthesized for highly efficient solid-phase derivatization of sugar phosphates. Sugar phosphates were selectively captured onto the surface of the SiO2@PD-Ti(4+) microspheres by chelating with phosphate groups, and then reacted with 3-amino-9-ethylcarbazole via reductive amination based on solid-phase derivatization, which could not only increase the retention and resolution of sugar phosphates on reversed-phase liquid chromatography (RPLC), but also improve the mass spectrometry (MS) sensitivity of sugar phosphates. The adsorption capacity of SiO2@PD-Ti(4+) microspheres towards glucose-6-phosphate is 0.76mg/g, which is much larger than that of commercial TiO2. Compared with the traditional liquid-phase derivatization, the solid-phase derivatization based on the SiO2@PD-Ti(4+) microspheres displayed several superiorities including shorter derivatization time (within 10min), higher product purity and much lower limit of detection (up to 38pmol/L). In addition, good linearity (R(2)≥0.99), excellent recovery (80.6-118%) and high precision (RSDs with 2.8-7.8%) were obtained when the developed method was used for quantitative analysis of sugar phosphates. Finally, the SiO2@PD-Ti(4+) microspheres combined with RPLC-MS were successfully applied to the determination of sugar phosphates from hepatocarcinoma cell lines and could even detect the trace sugar phosphates in thousands of cells. Copyright © 2016 Elsevier B.V. All rights reserved.

  12. Note: CO₂-mineral dissolution experiments using a rocking autoclave and a novel titanium reaction cell.

    Science.gov (United States)

    Purser, Gemma; Rochelle, Christopher A; Wallis, Humphrey C; Rosenqvist, Jörgen; Kilpatrick, Andrew D; Yardley, Bruce W D

    2014-08-01

    A novel titanium reaction cell has been constructed for the study of water-rock-CO2 reactions. The reaction cell has been used within a direct-sampling rocking autoclave and offers certain advantages over traditional "flexible gold/titanium cell" approaches. The main advantage is robustness, as flexible cells are prone to rupture on depressurisation during gas-rich experiments. The reaction cell was tested in experiments during an inter-laboratory comparison study, in which mineral kinetic data were determined. The cell performed well during experiments up to 130 °C and 300 bars pressure. The data obtained were similar to those of other laboratories participating in the study, and also to previously published data.

  13. Association of calcium and phosphate ions with collagen in the mineralization of vertebrate tissues.

    Science.gov (United States)

    Landis, William J; Jacquet, Robin

    2013-10-01

    Among the vertebrate species, collagen is the most abundant protein and is associated with mineralization of their skeleton and dentition in all tissues except enamel. In such tissues, bones, calcifying tendon, dentin, and cementum are comprised principally of type I collagen, which has been proposed as a template for apatite mineral formation. Recent considerations of the interaction between type I collagen and calcium and phosphate ions as the major constituents of apatite have suggested that collagen polypeptide stereochemistry underlies binding of these ions at sites within collagen hole and overlap regions and leads to nucleation of crystals. The concept is fundamental to understanding both normal and abnormal mineralization, and it is reviewed in this article. Given this background, avenues for additional research studies in vertebrate mineralization will also be described. The latter include, for instance, how mineralization events subsequent to nucleation, that is, crystal growth and development, occur and whether they, too, are directed by collagen stereochemical parameters; whether mineralization can be expected in all spaces between collagen molecules; whether the side chains of charged amino acid residues actually point toward and into the hole and overlap collagen spaces to provide putative binding sites for calcium and phosphate ions; and what phenomena may be responsible for mineralization beyond hole and overlap zones and into extracellular tissue regions between collagen structural units. These questions will be discussed to provide a broader understanding of collagen contributions to potential mechanisms of vertebrate mineralization.

  14. Fabrication of calcium phosphate films for coating on titanium substrates heated up to 773 K by RF magnetron sputtering and their evaluations

    Energy Technology Data Exchange (ETDEWEB)

    Ueda, Kyosuke [Department of Materials Processing, Tohoku University, 6-6-02 Aza Aoba, Aramaki, Aoba-ku, Sendai, Miyagi 980-8579 (Japan); Narushima, Takayuki [Tohoku University Biomedical Engineering Research Organization, 6-6-02 Aza Aoba, Aramaki, Aoba-ku, Sendai, Miyagi 980-8579 (Japan); Goto, Takashi [Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Taira, Masayuki [Department of Dental Materials and Technology, Iwate Medical University School of Dentistry, 1-3-27 Chuo-dori, Morioka, Iwate 020-8505 (Japan); Katsube, Tomoyuki [Tohoku University Biomedical Engineering Research Organization, 6-6-02 Aza Aoba, Aramaki, Aoba-ku, Sendai, Miyagi 980-8579 (Japan)

    2007-09-15

    Calcium phosphate films were fabricated on titanium substrates heated up to 773 K using radiofrequency (RF) magnetron sputtering. The deposition rate, phase and preferred orientation of the calcium phosphate films were studied. Immersion tests for the films were conducted using Hanks' solution and PBS(-), and the surface reactions on the specimens coated with the calcium phosphate films were investigated. The bonding strength between the coating films and the titanium substrates before and after the immersion tests was evaluated; the bonding strength decreased after the immersion tests. The alkaline phosphatase (ALP) activity of SaOS-2 cells on a titanium plate coated with a calcium phosphate film was examined by conducting a culture test. Calcium phosphate coating increased the ALP activity of SaOS-2 cells cultured for 3 and 7 days. Titanium cylinders were coated with an amorphous calcium phosphate film and implanted into the mandibles of beagle dogs. An increase in the extent of bone-implant contact for the coated titanium cylinders was confirmed 8 to 12 weeks after implantation and compared with the case for uncoated titanium cylinders.

  15. Nanoscale Phase Stability Reversal During the Nucleation and Growth of Titanium Oxide Minerals

    Science.gov (United States)

    Hummmer, D. R.; Heaney, P. J.; Kubicki, J. D.; Kent, P. R.; Post, J. E.

    2008-12-01

    Fine-grained titanium oxide minerals are important in soils, where they affect a variety of geochemical processes. They are also industrially important as catalysts, pigments, food additives, and dielectrics. Recent research has indicated an apparent reversal of thermodynamic stability between TiO2 phases at the nanoscale thought to be caused by an increased contribution of surface energy to the total free energy. Time-resolved X-ray diffraction (XRD) experiments in which titanium oxides crystallize from aqueous TiCl4 solutions confirm that anatase, a metastable phase, is always the first phase to nucleate under our range of initial conditions. Rutile peaks are observed only minutes after the first appearance of anatase, after which anatase abundance slowly decreases while rutile continues to form. Whole pattern refinement of diffraction data reveals that lattice constants of both phases increase throughout the crystallization process. In addition, transmission electron microscope (TEM) observations and kinetic modeling indicate that anatase does not undergo a solid-state transformation to the rutile structure as once thought. Instead, anatase appears to re-dissolve and then feed the growth of already nucleated rutile nanocrystals. Density functional theory (DFT) calculations were employed to model 1, 2, and 3 nm particles of both mineral phases. The total surface energies calculated from these models did yield lower values for anatase than for rutile by 8-13 kJ/mol depending on particle size, indicating that surface free energy is sufficient to account for stability reversal. However, these whole-particle surface energies were much higher than the sum of energies of each particle's constituent crystallographic surfaces. We attribute the excess energy to defects associated with the edges and corners of nanoparticles, which are not present on a 2-D periodic surface. This previously unreported edge and corner energy may play a dominant role in the stability reversal

  16. Thermally unstable complexants/phosphate mineralization of actinides

    Energy Technology Data Exchange (ETDEWEB)

    Nash, K. [Argonne National Lab., IL (United States)

    1996-10-01

    In situ immobilization is an approach to isolation of radionuclides from the hydrosphere that is receiving increasing attention. Rather than removing the actinides from contaminated soils, this approach transforms the actinides into intrinsically insoluble mineral phases resistant to leaching by groundwater. The principal advangates of this concept are the low cost and low risk of operator exposure and/or dispersion of the radionuclides to the wider environment. The challenge of this approach is toe accomplish the immobilization without causing collateral damage to the environment (the cure shouldn`t be worse than the disease) and verification of system performance.

  17. Biomimetic nanoparticles with polynucleotide and PEG mixed-monolayers enhance calcium phosphate mineralization

    Energy Technology Data Exchange (ETDEWEB)

    Vasconcellos, Kayla B.; McHugh, Sean M.; Dapsis, Katherine J.; Petty, Alexander R.; Gerdon, Aren E., E-mail: gerdoar@emmanuel.edu [Emmanuel College (United States)

    2013-09-15

    Biomineralization of hydroxyapatite (Ca{sub 10}(PO{sub 4}){sub 6}(OH){sub 2}) is of significant importance in biomedical applications such as bone and dental repair, and biomimetic control of mineral formation may lead to more effective restorative procedures. Gold nanoparticles are functional scaffolds on which to assemble multi-component monolayers capable of mimicking protein activity in the templated synthesis of calcium phosphate. The goal of this research was to explore nanoparticle templates with mixed-monolayers of uncharged polar polyethylene glycol (PEG) molecules and highly charged polynucleotide and amino acid molecules in their ability to influence mineralization rates and mineral particle size and morphology. This research demonstrates through time-resolved optical density and dynamic light scattering measurements that the combination of tiopronin, PEG, and DNA presented on a nanoparticle surface decreases nanoparticle aggregation from 59 to 21 nm solvated radius, increases mineralization kinetics from 1.5 Multiplication-Sign 10{sup -3} to 3.1 Multiplication-Sign 10{sup -3} OD/min, and decreases mineral particle size from 685 to 442 nm average radius. FT-IR and TEM data demonstrate that mineralized material, while initially amorphous, transforms to a semi-crystalline material when guided by template interactions. This demonstrates that surface-tailored monolayer protected cluster scaffolds are successful and controllable mineralization templates with further potential for biomedical applications involving calcium phosphate and other biomaterials.

  18. Biomimetic nanoparticles with polynucleotide and PEG mixed-monolayers enhance calcium phosphate mineralization

    Science.gov (United States)

    Vasconcellos, Kayla B.; McHugh, Sean M.; Dapsis, Katherine J.; Petty, Alexander R.; Gerdon, Aren E.

    2013-09-01

    Biomineralization of hydroxyapatite (Ca10(PO4)6(OH)2) is of significant importance in biomedical applications such as bone and dental repair, and biomimetic control of mineral formation may lead to more effective restorative procedures. Gold nanoparticles are functional scaffolds on which to assemble multi-component monolayers capable of mimicking protein activity in the templated synthesis of calcium phosphate. The goal of this research was to explore nanoparticle templates with mixed-monolayers of uncharged polar polyethylene glycol (PEG) molecules and highly charged polynucleotide and amino acid molecules in their ability to influence mineralization rates and mineral particle size and morphology. This research demonstrates through time-resolved optical density and dynamic light scattering measurements that the combination of tiopronin, PEG, and DNA presented on a nanoparticle surface decreases nanoparticle aggregation from 59 to 21 nm solvated radius, increases mineralization kinetics from 1.5 × 10-3 to 3.1 × 10-3 OD/min, and decreases mineral particle size from 685 to 442 nm average radius. FT-IR and TEM data demonstrate that mineralized material, while initially amorphous, transforms to a semi-crystalline material when guided by template interactions. This demonstrates that surface-tailored monolayer protected cluster scaffolds are successful and controllable mineralization templates with further potential for biomedical applications involving calcium phosphate and other biomaterials.

  19. Titanium phosphate glass microcarriers induce enhanced osteogenic cell proliferation and human mesenchymal stem cell protein expression

    Directory of Open Access Journals (Sweden)

    Nilay J Lakhkar

    2015-11-01

    Full Text Available In this study, we have developed 50- to 100-µm-sized titanium phosphate glass microcarriers (denoted as Ti5 that show enhanced proliferation of human mesenchymal stem cells and MG63 osteosarcoma cells, as well as enhanced human mesenchymal stem cell expression of bone differentiation markers, in comparison with commercially available glass microspheres at all time points. We also demonstrate that these microcarriers provide superior human mesenchymal stem cell proliferation with conventional Dulbecco’s Modified Eagle medium than with a specially developed commercial stem cell medium. The microcarrier proliferative capacity is revealed by a 24-fold increase in MG63 cell numbers in spinner flask bioreactor studies performed over a 7-day period, versus only a 6-fold increase in control microspheres under the same conditions; the corresponding values of Ti5 and control microspheres under static culture are 8-fold and 7-fold, respectively. The capability of guided osteogenic differentiation is confirmed by ELISAs for bone morphogenetic protein-2 and osteopontin, which reveal significantly greater expression of these markers, especially osteopontin, by human mesenchymal stem cells on the Ti5 microspheres than on the control. Scanning electron microscopy and confocal laser scanning microscopy images reveal favorable MG63 and human mesenchymal stem cell adhesion on the Ti5 microsphere surfaces. Thus, the results demonstrate the suitability of the developed microspheres for use as microcarriers in bone tissue engineering applications.

  20. Does Salivary Calcium and Phosphate Concentrations Adequately Reflect Bone Mineral Density in Patients with Chronic Periodontitis?

    Science.gov (United States)

    Moghadam, Somaye Ansari; Zakeri, Zahra; Fakour, Sirous Risbaf; Moghaddam, Alireza Ansari

    2016-10-01

    Periodontitis is the inflammation of the periodontal supporting tissues. The response of periodontal tissues to local bacteria leads to bone resorption and destruction of periodontal junction. Given the possible association between periodontitis and low bone mineral density, the aim of present study was to find if measurement of salivary biomarkers as a less invasive method, can provide an appropriate screening method for assessment of bone mineral density in patients with chronic periodontitis? A case-control study was conducted on 53 people, including 28 patients with severe chronic periodontitis and 25 healthy people between April 2014 to March 2015 in Zahedan (southeast of Iran). Following Periodontal examination, salivary samples were collected, and the concentration of salivary calcium and phosphate were measured and reported as mg/dl. Bone mineral density of participants was measured using dual energy x-ray absorptiometry and reported as gr/cm2. No significant association was found between concentrations of salivary calcium and phosphate levels with bone mineral density in either healthy people or in patients with severe chronic periodontitis, despite a significant bone density reduction (in the femur neck and lumbar spine L2-L4) in the periodontitis group compared to healthy people (P=0.006, and P=0.009 respectively). Concentration of salivary calcium and phosphate do not appear to be good indicators of bone mineral density. Further prospective studies with larger sample size are recommended.

  1. Removal of phosphate ions from aqueous solution using Tunisian clays minerals and synthetic zeolite

    Institute of Scientific and Technical Information of China (English)

    Noureddine Hamdi; Ezzeddine Srasra

    2012-01-01

    Phosphate ions are usually considered to be responsible for the algal bloom in receiving water bodies and aesthetic problems in water.From the environmental point of view,the management of such contaminant and valuable resource is very important.The present work deals with the removal of phosphate ions from aqueous solutions using kaolinitic and smectic clay minerals and synthetic zeolite as adsorbent.The pH effect and adsorption kinetic were studied.It was found that phosphate could be efficiently removed at acidic pH (between 4 and 6) and the second order model of kinetics is more adopted for all samples.The isotherms of adsorption of phosphate ions by the two clays and the zeolite samples show that the zeolite has the highest rate of uptake (52.9 mg P/g).Equilibrium data were well fitted with Langmuir and Freundlich isotherm.

  2. Effect of polydopamine on the biomimetic mineralization of mussel-inspired calcium phosphate cement in vitro

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Zongguang [Key Lab of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Qu, Shuxin, E-mail: qushuxin@swjtu.edu.cn [Key Lab of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Zheng, Xiaotong; Xiong, Xiong [Key Lab of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Fu, Rong; Tang, Kuangyun; Zhong, Zhendong [Department of Plastic Surgery, Academy of Medical Sciences and Sichuan Provincial People' s Hospital, Chengdu 610041 (China); Weng, Jie [Key Lab of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China)

    2014-11-01

    Inspired by the excellent adhesive property of mussel adhesive protein, we added polydopamine (PDA) to calcium phosphate cement (PDA–CPC) to enhance its compressive strength previously. The mineralization and mechanism on PDA–CPC were investigated by soaking it in simulated body fluid in this study. The results indicated that PDA promoted the conversion of dicalcium phosphate dihydrate and α-tricalcium phosphate to hydroxyapatite (HA) in the early stage but inhibited this conversion subsequently. PDA promoted the rapid mineralization on PDA–CPC to form a layer of nanoscale calcium phosphate (CaP) whereas there was no CaP formation on the control-CPC after 1 d of soaking. This layer of nanoscale CaP was similar to that of natural bone, which was always observed during soaking. X-ray photoelectron spectroscopy showed that the peak of C=O of PDA existed in the newly formed CaP on PDA–CPC, indicating the co-precipitation of CaP with PDA. Furthermore, the newly formed CaP on PDA–CPC was HA confirmed by transmission electron microscopy, which the newly formed HA was in association with PDA. Therefore, PDA increased the capacity of mineralization of CPC and induced the formation of nanoscale bone-like apatite on PDA–CPC. Thus, this provides the feasible route for surface modification on CPC. - Highlights: • Effect of polydopamine (PDA) on the in vitro mineralization of PDA-CPC was studied. • PDA promoted the rapid mineralization on PDA-CPC to form a nanoscale HA layer. • The precipitation of the nanoscale HA layer on PDA-CPC accompanied with PDA. • Polydopamine induced mineralization is feasible for surface modification of CaP.

  3. Synthesis of soluble phosphate polymers by RAFT and their in vitro mineralization.

    Science.gov (United States)

    Suzuki, Shuko; Whittaker, Michael R; Grøndahl, Lisbeth; Monteiro, Michael J; Wentrup-Byrne, Edeline

    2006-11-01

    Soluble linear (non-cross-linked) poly(monoacryloxyethyl phosphate) (PMAEP) and poly(2-(methacryloyloxy)ethyl phosphate) (PMOEP) were successfully synthesized through reversible addition-fragmentation chain transfer (RAFT)-mediated polymerization and by keeping the molecular weight below 20 K. Above this molecular weight, insoluble (cross-linked) polymers were observed, postulated to be due to residual diene (cross-linkable) monomers formed during purification of the monomers, MOEP and MAEP. Block copolymers consisting of PMAEP or PMOEP and poly(2-(acetoacetoxy)ethyl methacrylate) (PAAEMA) were successfully prepared and were immobilized on aminated slides. Simulated body fluid studies revealed that calcium phosphate (CaP) minerals formed on both the soluble polymers and the cross-linked gels were very similar. Both the PMAEP polymers and the PMOEP gel showed a CaP layer most probably brushite or monetite based on the Ca/P ratios. A secondary CaP mineral growth with a typical hydroxyapatite (HAP) globular morphology was found on the PMOEP gel. The soluble PMOEP film formed carbonated HAP according to Fourier transform infrared (FTIR) spectroscopy. Block copolymers attached to aminated slides showed only patchy mineralization, possibly due to the ionic interaction of negatively charged phosphate groups and protonated amines.

  4. Paracrystalline Disorder from Phosphate Ion Orientation and Substitution in Synthetic Bone Mineral

    Energy Technology Data Exchange (ETDEWEB)

    Marisa, Mary E.; Zhou, Shiliang; Melot, Brent C.; Peaslee, Graham F.; Neilson, James R.

    2016-12-05

    Hydroxyapatite is an inorganic mineral closely resembling the mineral phase in bone. However, as a biological mineral, it is highly disordered, and its composition and atomistic structure remain poorly understood. Here, synchrotron X-ray total scattering and pair distribution function analysis methods provide insight into the nature of atomistic disorder in a synthetic bone mineral analogue, chemically substituted hydroxyapatite. By varying the effective hydrolysis rate and/or carbonate concentration during growth of the mineral, compounds with varied degrees of paracrystallinity are prepared. From advanced simulations constrained by the experimental pair distribution function and density functional theory, the paracrystalline disorder prevalent in these materials appears to result from accommodation of carbonate in the lattice through random displacement of the phosphate groups. Though many substitution modalities are likely to occur in concert, the most predominant substitution places carbonate into the mirror plane of an ideal phosphate site. Understanding the mineralogical imperfections of a biologically analogous hydroxyapatite is important not only to potential bone grafting applications but also to biological mineralization processes themselves.

  5. New hydrogen titanium phosphate sulfate electrodes for Li-ion and Na-ion batteries

    Science.gov (United States)

    Zhao, Ran; Mieritz, Daniel; Seo, Dong-Kyun; Chan, Candace K.

    2017-03-01

    NASICON-type materials with general formula AxM2(PO4)3 (A = Li or Na, M = Ti, V, and Fe) are promising candidates for Li- and Na-ion batteries due to their open three-dimensional framework structure. Here we report the electrochemical properties of hydrogen titanium phosphate sulfate, H0.4Ti2(PO4)2.4(SO4)0.6 (HTPS), a new mixed polyanion material with NASICON structure. Micron-sized HTPS aggregates with crystallite grain size of ca. 23 nm are synthesized using a sol-gel synthesis in an acidic medium. The properties of the as-synthesized HTPS, ball-milled HTPS, and samples prepared as carbon composites using an in-situ glucose decomposition reaction are investigated. A capacity of 148 mAh g-1 corresponding to insertion of 2 Li+ per formula unit is observed in the ball-milled HTPS over the potential window of 1.5-3.4 V vs. Li/Li+. Lithiation at ca. 2.8 and 2.5 V is determined to occur through filling of the M1 and M2 sites, respectively. Powder X-ray diffraction (PXRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) are used characterize the HTPS before and after cycling. Evaluation of the HTPS in a Na-ion cell is also performed. A discharge capacity of 93 mAh g-1 with sodiation at ca. 2.9 and 2.2 V vs. Na/Na+ is observed.

  6. EFFECTS OF MINERAL AND ORGANIC-MINERAL PHOSPHATE FERTILIZERS ON SOIL FERTILITY PARAMETERS

    Directory of Open Access Journals (Sweden)

    Diego Henriques

    2013-06-01

    Full Text Available Organic sources can replace all or part of the mineral phosphorus used in fertilizer, providing significant changes in soil chemical properties. This research evaluated the effects of mineral and organic-mineral phosphorus on the soil fertility in maize tillage. The experiment was installed in a seedling nursery at Universidade do Oeste Paulista in Presidente Prudente-SP, in a complete randomized blocks design, with 9 treatments (different Biofós doses associated with different superphosphate doses and 4 replicates. As phosphorus fertilizer source was used the organic-mineral Biofós (3.8% P2O5 and simple superphosphate (18% P2O5. At 50 days after emergence of corn plants it was held soil sampling vessels for evaluation of phosphorus, organic matter, calcium, magnesium, base saturation and soil pH. The fertilizer organic-mineral showed the same efficiency of simple superphosphate in soil fertility. The organo-mineral fertilizer showed the same efficiency of superphosphate on soil fertility, both of which promoted the same changes in pH. Higher Biofós doses should have high levels of soil organic matter, which was not observed. Phosphorus, calcium, magnesium and base saturation level did not differ in all fertilizer sources and levels used.

  7. Chapter 9: Model Systems for Formation and Dissolution of Calcium Phosphate Minerals

    Energy Technology Data Exchange (ETDEWEB)

    Orme, C A; Giocondi, J L

    2006-07-29

    Calcium phosphates are the mineral component of bones and teeth. As such there is great interest in understanding the physical mechanisms that underlie their growth, dissolution, and phase stability. Control is often achieved at the cellular level by the manipulation of solution states and the use of crystal growth modulators such as peptides or other organic molecules. This chapter begins with a discussion of solution speciation in body fluids and relates this to important crystal growth parameters such as the supersaturation, pH, ionic strength and the ratio of calcium to phosphate activities. We then discuss the use of scanning probe microscopy as a tool to measure surface kinetics of mineral surfaces evolving in simplified solutions. The two primary themes that we will touch on are the use of microenvironments that temporally evolve the solution state to control growth and dissolution; and the use of various growth modifiers that interact with the solution species or with mineral surfaces to shift growth away from the lowest energy facetted forms. The study of synthetic minerals in simplified solution lays the foundation for understand mineralization process in more complex environments found in the body.

  8. Regulation of in vitro calcium phosphate mineralization by combinatorially selected hydroxyapatite-binding peptides.

    Science.gov (United States)

    Gungormus, Mustafa; Fong, Hanson; Kim, Il Won; Evans, John Spencer; Tamerler, Candan; Sarikaya, Mehmet

    2008-03-01

    We report selection and characterization of hydroxyapatite-binding heptapeptides from a peptide-phage library and demonstrate the effects of two peptides, with different binding affinities and structural properties, on the mineralization of calcium phosphate mineral. In vitro mineralization studies carried out using one strong- and one weak-binding peptide, HABP1 and HABP2, respectively, revealed that the former exhibited a drastic outcome on mineralization kinetics and particle morphology. Strong-binding peptide yielded significantly larger crystals, as observed by electron microscopy, in comparison to those formed in the presence of a weak-binding peptide or in the negative control. Molecular structural studies carried out by circular dichroism revealed that HABP1 and HABP2 differed in their secondary structure and conformational stability. The results indicate that sequence, structure, and molecular stability strongly influence the mineralization activity of these peptides. The implication of the research is that the combinatorially selected short-sequence peptides may be used in the restoration or regeneration of hard tissues through their control over of the formation of calcium phosphate biominerals.

  9. Chemical analysis of uranium and titanium niobotantalate metamict minerals by ion-exchange chromatography and spectrophotometric procedures

    Energy Technology Data Exchange (ETDEWEB)

    Mazzucotelli, A. (Genoa Univ. (Italy). Ist. di Chimica Generale); Vannucci, R. (Urbino Univ. (Italy). Ist. di Mineralogia e Petrografia); Vannucci, S. (Consiglio Nazionale delle Ricerche, Florence (Italy). Centro Studi Mineralogia e Geochimica dei Sedimenti); Passaglia, E. (Ferrara Univ. (Italy). Ist. di Mineralogia)

    1984-03-01

    An ion-exchange separation followed by spectrophotometric determinations is applied to some metamict minerals. These minerals, containing very high amounts of elements which present some problems to the analyst, such as uranium, titanium, niobium and rare-earth elements, are fused with potassium bisulphate, and the cooled melts dissolved in sulphuric acid. The solutions are passed through a series of three ion-exchange columns to separate those mineral-forming elements for which the colorimetric procedures suffer interference from the elements listed above. The procedure has been tested with a synthetic solution and with solutions of the minerals.

  10. Procedure for the study of acidic calcium phosphate precursor phases in enamel mineral formation.

    Science.gov (United States)

    Siew, C; Gruninger, S E; Chow, L C; Brown, W E

    1992-02-01

    Considerable evidence suggests that an acidic calcium phosphate, such as octacalcium phosphate (OCP) or brushite, is involved as a precursor in enamel and other hard tissue formation. Additionally, there is in vitro evidence suggesting that fluoride accelerates and magnesium inhibits the hydrolysis of OCP to hydroxyapatite (OHAp). As the amount of OCP or brushite in enamel cannot be measured directly in the presence of an excess of hydroxyapatite, a procedure was developed that allows for their indirect in vivo quantification as pyrophosphate. This permits study of the effects of fluoride and magnesium ions on enamel mineral synthesis. Rat incisor calcium phosphate was labeled by intraperitoneal injection of NaH2(32)PO4. The rats were then subjected to various fluoride and magnesium treatments with subcutaneous implanted osmotic pumps. They were then killed at predetermined intervals; the nascent sections of the incisors were collected, cleaned, and pyrolyzed at 500 degrees C for 48 hours to convert acidic calcium phosphates to calcium pyrophosphate; the pyrophosphate was separated from orthophosphate by anion-exchange chromatography; and the resulting fractions were counted by liquid scintillation spectrometry. The activities of the pyro- and orthophosphate fractions were used to calculate the amount of acidic calcium phosphate present in the nascent mineral. The results demonstrated that the percentage of radioactive pyrophosphate in nascent incisors decreased with time, with increasing serum F- concentration, and with decreasing serum magnesium content. The technique described here should prove to be a powerful new tool for studying the effects of various agents on biological mineral formation.

  11. Type II Na+-Pi cotransporters in osteoblast mineral formation: regulation by inorganic phosphate.

    Science.gov (United States)

    Lundquist, Patrik; Murer, Heini; Biber, Jürg

    2007-01-01

    During calcification of bone, large amounts of phosphate (P(i)) must be transported from the circulation to the osteoid. Likely candidates for osteoblast P(i) transport are the type II sodium-phosphate cotransporters NaPi-IIa and NaPi-IIb that facilitate transcellular P(i) flux in kidney and intestine, respectively. We have therefore determined the 'cotransporters' expression in osteoblast-like cells. We have also studied the 'cotransporters' regulation by P(i) and during mineralization in vitro. Phosphate uptake and cotransporter protein expression was investigated at early, late and mineralizing culture stages of mouse (MC3T3-E1) and rat (UMR-106) osteoblast-like cells. Both NaPi-IIa and NaPi-IIb were expressed by both osteoblast-like cell lines. NaPi-IIa was upregulated in both cell lines one week after confluency. After 7 days in 3mM P(i) NaPi-IIa was strongly upregulated in both cell lines. NaPi-IIb expression was unaffected by both culture stage and P(i) supplementation. The expression of both cotransporters was unaffected by P(i) deprivation. In vitro mineralization at 1.5mM P(i) was preceded by a three-fold increase in osteoblast sodium-dependent P(i) uptake and a corresponding upregulation of both NaPi-IIa and NaPi-IIb. Their expression thus seem regulated by phosphate in a manner consistent with their playing a role in transcellular P(i) flux during mineralization.

  12. Water-Soluble Cellulose Derivatives Are Sustainable Additives for Biomimetic Calcium Phosphate Mineralization

    OpenAIRE

    2016-01-01

    The effect of cellulose-based polyelectrolytes on biomimetic calcium phosphate mineralization is described. Three cellulose derivatives, a polyanion, a polycation, and a polyzwitterion were used as additives. Scanning electron microscopy, X-ray diffraction, IR and Raman spectroscopy show that, depending on the composition of the starting solution, hydroxyapatite or brushite precipitates form. Infrared and Raman spectroscopy also show that significant amounts of nitrate ions are incorporated i...

  13. Phosphates (V) recovery from phosphorus mineral fertilizers industry wastewater by continuous struvite reaction crystallization process.

    Science.gov (United States)

    Hutnik, Nina; Kozik, Anna; Mazienczuk, Agata; Piotrowski, Krzysztof; Wierzbowska, Boguslawa; Matynia, Andrzej

    2013-07-01

    Continuous DT MSMPR (Draft Tube Mixed Suspension Mixed Product Removal) crystallizer was provided with typical wastewater from phosphorus mineral fertilizers industry (pH phosphate(V) ions decreased from 0.445 to 9.2 × 10(-4) mass %. This can be regarded as a very good process result. In product crystals, besides main component - struvite, all impurities from wastewater were detected analytically.

  14. Artificial citrate operon and Vitreoscilla hemoglobin gene enhanced mineral phosphate solubilizing ability of Enterobacter hormaechei DHRSS.

    Science.gov (United States)

    Yadav, Kavita; Kumar, Chanchal; Archana, G; Kumar, G Naresh

    2014-10-01

    Mineral phosphate solubilization by bacteria is mediated through secretion of organic acids, among which citrate is one of the most effective. To overproduce citrate in bacterial systems, an artificial citrate operon comprising of genes encoding NADH-insensitive citrate synthase of E. coli and Salmonella typhimurium sodium-dependent citrate transporter was constructed. In order to improve its mineral phosphate solubilizing (MPS) ability, the citrate operon was incorporated into E. hormaechei DHRSS. The artificial citrate operon transformant secreted 7.2 mM citric acid whereas in the native strain, it was undetectable. The transformant released 0.82 mM phosphate in flask studies in buffered medium containing rock phosphate as sole P source. In fermenter studies, similar phenotype was observed under aerobic conditions. However, under microaerobic conditions, no citrate was detected and P release was not observed. Therefore, an artificial citrate gene cluster containing Vitreoscilla hemoglobin (vgb) gene under its native promoter, along with artificial citrate operon under constitutive tac promoter, was constructed and transformed into E. hormaechei DHRSS. This transformant secreted 9 mM citric acid under microaerobic conditions and released 1.0 mM P. Thus, incorporation of citrate operon along with vgb gene improves MPS ability of E. hormaechei DHRSS under buffered, microaerobic conditions mimicking rhizospheric environment.

  15. The geology of aluminium phosphates and sulphates of the alunite group minerals: a review

    Science.gov (United States)

    Dill, Harald G.

    2001-03-01

    Aluminium phosphates and sulphates of the alunite supergroup (APS minerals) occur in a wide range of environments of formation covering the metamorphic, igneous and sedimentary realms. Supergene processes, including mineral dressing and dumping when sulphide ores are mined, as well as hypogene alteration are also responsible for the precipitation of APS minerals. In these environments, complex solid solution series (s.s.s.) can form. The general formula of these alunite minerals is AB 3 (XO 4) 2(OH) 6, where A is a large cation (Na, U, K, Ag, NH 4, Pb, Ca, Ba, Sr, REE). B sites are occupied by cations of the elements Al, Fe, Cu and Zn. In nature, the anion (XO 4) x- is dominated by P and S. Mineral dressing and identification of APS minerals often needs a combination of highly sophisticated measures including Atterberg settling methods, XRD, DTA, TGA, TEM-EDX, SEM, EMPA and XRF. In sedimentary rocks APS minerals occur in various rocks and environments of deposition: calcareous, phosphorite-bearing, argillaceous-carbonaceous, arenaceous, coal-bearing environments, in soils and paleosols, in saprolite (bauxites, laterites) and in calcareous-argillaceous sequences hosting Carlin-type SHDG deposits. In igneous rocks, APS minerals may be encountered mainly in acidic through intermediate pyroclastic, volcanic and subvolcanic rocks. They occur in barren volcanic rocks and porphyry-type intrusions that have sparked epithermal Au-Ag-base metal deposits, Au-Sb mineralization, APS-bearing argillite and alunite deposits in their immediate surroundings. Granitic and pegmatitic rocks are rarely host of supergene APS mineralization. During low-grade stage regional metamorphism, peraluminous parent rocks originating from a sedimentary or igneous protolith may also give rise to APS mineralization. Peraluminous parent rocks enriched in S and/or P are a prerequisite for the formation of APS minerals that are stable up to a temperature of 400°C at moderately high fluid pressure of up

  16. Adsorption of Acid Phosphatase on Minerals and Soil Colloids in Presence of Citrate and Phosphate

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The aim of this work was to study the influence of phosphate and citrate, which are common inorganic andorganic anions in soils, on the adsorption of acid phosphatase by kaolin, goethite and the colloids separatedfrom yellow-brown soil (YBS) and latosol (LS) in central-south China. The YBS colloid has the major claymineral composition of 1.4 nm mineral, illite and kaolinite while the LS colloid mainly contains kaolinite andoxides. The adsorption isotherm of acid phosphatase on the examined soil colloids and minerals fitted tothe Langmuir model. The amount of enzyme adsorbed in the absence of ligands was in the order of YBScolloid >LS colloid>kaolin≈goethite. In the presence of phosphate or citrate, the amounts of the enzymeadsorbed followed the sequence YBS colloid>kaolin>LS colloid>goethite. The presence of ligands alsodecreased the binding energy between the enzyme and soil colloids or minerals. With the increase of ligandconcentration from 10 mmol L-1 to 400 m mol L-1, different behaviors for the adsorption of enzyme werefound in the colloid and mineral systems studied. A sharp decrease in enzyme adsorption was observed ongoethite while gradual decreases of enzyme adsorption were recorded in the two soil colloid systems. However,no any decrease was found for the amount of enzyme adsorbed on kaolin at higher ligand concentrations.When phosphate or citrate was introduced to the system before the addition of enzyme, the ligands usuallyenhanced the adsorption of enzyme. The results obtained in this study suggested the important role ofkaolinite mineral in the adsorption of enzyme molecules in acidic soils in the presence of various ligands.

  17. Transformation of 1-D Chiral-chained Titanium Phosphate to 2-D Layer Structure Through a 1-D Zigzag Chain

    Institute of Scientific and Technical Information of China (English)

    CHEN Chao; YANG Yu-lin; LI Wei-sheng; LIU Yun-ling; YI Zhuo; GUO Yang-hong; PANG Wen-qin

    2005-01-01

    The transformation of titanium phosphate from 1-D chiral- chain(JTP-A) to 2-D layer(TP-J1) has been carefully investigated. Through a hydrolysis-condensation self-assembly pathway, the crystals of TP-J1 can be obtained from the JTP-A phase under hydrothermal conditions. An intermediate material with zigzag chain during the transformation was observed by XRD characterization. A hypothesis of the transformation mechanism is also described in this article. It is noteworthy that ethylenediamine plays an important role in the transformation.

  18. Trace elements in rock phosphates and P containing mineral and organo-mineral fertilizers sold in Germany

    Energy Technology Data Exchange (ETDEWEB)

    Kratz, Sylvia, E-mail: sylvia.kratz@jki.bund.de; Schick, Judith; Schnug, Ewald

    2016-01-15

    68 rock phosphates and 162 P containing (organo-)mineral fertilizers sold in Germany were evaluated with regard to trace element contents. While Al, As, B, Be, Cd, Cr, Mo, Ni, Pb, Sb, Se, Tl, U, and Zn were higher in sedimentary than in igneous rock phosphates, the opposite was true for Co, Cu, Sn, Mn, Ti, Fe, and Sr. Comparing element concentrations to the currently valid legal limit values defined by the German Fertilizer Ordinance, it was found that some PK and many straight P fertilizers (superphosphate, triple superphosphate, partly acidulated rock phosphates) exceeded the limit of 50 mg Cd/kg P{sub 2}O{sub 5}. Mean values for As, Ni, Pb, and Tl remained below legal limits in almost all cases. While no legal limit has been defined for U in Germany yet, the limit of 50 mg U/kg P{sub 2}O{sub 5} for P containing fertilizers proposed by the German Commission for the Protection of Soils was clearly exceeded by mean values for all fertilizer types analyzed. A large share of the samples evaluated in this work contained essential trace elements at high concentrations, with many of them not being declared as such. Furthermore, trace elements supplied with these fertilizers at a fertilization rate leveling P uptake would exceed trace element uptake by crops. This may become most relevant for B and Fe, since many crops are sensitive to an oversupply of B, and Fe loads exceeding plant uptake may immobilize P supplies for the crops by forming Fe phosphate salts. The sample set included two products made from thermochemically treated sewage sludge ash. The products displayed very high concentrations of Fe and Mn and exceeded the legal limit for Ni, emphasizing the necessity to continue research on heavy metal removal from recycled raw materials and the development of environmentally friendly and agriculturally efficient fertilizer products. - Highlights: • Mineral fertilizers (MF) sold in Germany often exceed legal limits for Cd • MF sold in Germany contain high

  19. Ethyl methanesulfonate mutagenesis-enhanced mineral phosphate solubilization by groundnut-associated Serratia marcescens GPS-5.

    Science.gov (United States)

    Tripura, Chaturvedula; Sashidhar, Burla; Podile, Appa Rao

    2007-02-01

    Twenty-three bacterial isolates were screened for their mineral phosphate-solubilizing (MPS) ability on Pikovskaya and National Botanical Research Institute's phosphate (NBRIP) agar. The majority of the isolates exhibited a strong ability to solubilize hydroxyapatite in both solid and liquid media. The solubilization in liquid medium corresponded with a decrease in the pH of the medium. Serratia marcescens GPS-5, known for its biocontrol of late leaf spot in groundnut, emerged as the best solubilizer. S. marcescens GPS-5 was subjected to ethyl methanesulfonate (EMS) mutagenesis, and a total of 1700 mutants, resulting after 45 minutes of exposure, were screened on buffered NBRIP medium for alterations in MPS ability compared with that of the wild type. Seven mutants with increased (increased-MPS mutants) and 6 mutants with decreased (decreased-MPS mutants) MPS ability were isolated. All seven increased-MPS mutants were efficient at solubilizing phosphate in both solid and liquid NBRIP medium. Among the increased-MPS mutants, EMS XVIII Sm-35 showed the maximum (40%) increase in the amount of phosphate released in liquid medium compared with wild-type S. marcescens GPS-5, therefore, it would be a useful microbial inoculant in groundnut cultivation. EMS III Sm W, a nonpigmented mutant, showed the lowest solubilization of phosphate among the 6 decreased-MPS mutants.

  20. Influence of titanium ion on mineral formation and properties of osteoid nodules in rat calvaria cultures.

    Science.gov (United States)

    Liao, H; Wurtz, T; Li, J

    1999-11-01

    The effect of the addition of titanium ion (Ti) on osteoblast function and the mineralization of osteoid nodules in rat calvaria cultures was characterized. Concentrations of 10 ppm of Ti or more inhibited cell proliferation; 5 ppm or less either had no effect or stimulated proliferation. The number of nodules formed was not influenced by 5 ppm of Ti, but mineral deposition in nodules was suppressed, as revealed by von Kossa staining. Likewise, 5 ppm of Ti inhibited the incorporation of [(45)Ca] in cultures during nodule formation even if the Ti was withdrawn from the medium when mineralization was initiated. In order to test whether the synthesis of osteoid components was affected, the expression of osteonectin (OSN), osteopontin (OPN), osteocalcin (OSC), and alkaline phosphatase (ALP) mRNAs as well as ALP enzyme activity was analyzed. The expression of OSN and OPN mRNAs was reduced dramatically, but OSC mRNA was little affected by 5 ppm of Ti. Ti delayed the development of ALP mRNA expression and enzyme activity relative to the controls. Thus Ti treatment changed the proportional composition of cellular mRNA contributing the osteoblast phenotype.

  1. On the mineral characteristics and geochemistry of the Florida phosphate of Four Corners and Hardee County mines

    Science.gov (United States)

    Baghdady, Ashraf R.; Howari, Fares M.; Al-Wakeel, Mohamed I.

    2016-08-01

    The Florida phosphate deposits in Four Corners and Hardee County mines are composed mainly of phosphate minerals and quartz in addition to subordinate proportions of feldspars, dolomite, calcite, gypsum, kaolinite, attapulgite and montmorillonite. These phosphorites contain three structurally different types of mudclasts: massive mudclasts, mudclasts with concentric structure and mudclasts consisting of agglomerates of apatite microparticles. The latter are represented by particles resembling phosphatized fossil bacteria associated with microbial filaments, and hollow apatite particles having surfacial coatings and connected to microbial filaments. The Florida phosphate particles are reworked and vary in mineral composition, color and shape. They are composed of a mixture of well-crystalline species including carbonate fluorapatite (francolite), carbonate apatite and fluorapatite. The color variation of the phosphate particles is related to difference in mineral composition, extent of diagenetic effects and reworking. The light-colored mudclasts are characterized by the presence of carbonate apatite and aluminum hydroxide phosphate minerals, whereas the dark mudclasts are rich in iron aluminum hydroxide phosphate minerals. The Florida phosphorites are suggested to be formed partially by authigenetic precipitation, replacement of the sea floor carbonate and diatomite, and microbial processes. With respect to elemental geochemistry, the analyzed particles contain small percentages of sulfur and iron which are related to the occurrence of pyrite. Traces of silica and alumina are recorded which may be attributed to the diagenetic. Some of the tested particles are relatively rich in phosphorous, fluorine, calcium, and magnesium, while poor in silicon, potassium and sulfur. Whereas, the bioclasts (especially teeth) are relatively rich in calcium, phosphorous and fluorine while poor in silicon, aluminum, magnesium and potassium. Hence, the microchemical analyses revealed

  2. Cavitation Erosion of Copper, Brass, Aluminum and Titanium Alloys in Mineral Oil

    Science.gov (United States)

    Rao, B. C. S.; Buckley, D. H.

    1983-01-01

    The variations of the mean depth of penetration, the mean depth rate of penetration, MDRP, the pit diameter 2a and depth h due to cavitation attack on Al 6061-T6, Cu, brass of composition Cu-35Zn-3Pb and Ti-5A1-2.5Sn are presented. The experiments are conducted in a mineral oil of viscosity 110 CS using a magnetostrictive oscillator of 20 kHz frequency. Based on MDRP on the materials, it is found that Ti-5Al-2.5Sn exhibits cavitation erosion resistance which is two orders of magnitude higher than the other three materials. The values of h/a are the largest for copper and decreased with brass, titanium, and aluminum. Scanning electron microscope studies show that extensive slip and cross slip occurred on the surface prior to pitting and erosion. Twinning is also observed on copper and brass.

  3. Generally recognized as safe (GRAS) Lactococcus lactis strains associated with Lippia sidoides Cham. are able to solubilize/mineralize phosphate.

    Science.gov (United States)

    de Lacerda, Jackeline Rossetti Mateus; da Silva, Thais Freitas; Vollú, Renata Estebanez; Marques, Joana Montezano; Seldin, Lucy

    2016-01-01

    Eight strains isolated from the stems of Lippia sidoides were identified as belonging to Lactococcus lactis, a bacterial species considered as "generally recognized as safe". Their capacity to solubilize/mineralize phosphate was tested in vitro with different inorganic and organic phosphorus (P) sources. All strains were able to solubilize calcium phosphate as an inorganic P source, and the best result was observed with strain 003.41 which solubilized 31 % of this P source. Rock phosphate, a mined rock containing high amounts of phosphate bearing minerals, was solubilized by five strains. When calcium phytate was the organic P source used, the majority of the strains tested showed phosphate mineralization activity. Moreover, all strains were able to solubilize/mineralize phosphate from poultry litter, a complex P source containing inorganic and predominantly organic P. The presence of genes coding for phytase and alkaline phosphatase was searched within the strains studied. However, only gene sequences related to alkaline phosphatase (phoA and phoD) could be detected in the majority of the strains (excepting strain 006.29) with identities varying from 67 to 88 %. These results demonstrate for the first time the potential of L. lactis strains for phosphate solubilization/mineralization activity using a broad spectrum of P sources; therefore, they are of great importance for the future development of more safe bioinoculants with possible beneficial effects for agriculture.

  4. Trace elements in rock phosphates and P containing mineral and organo-mineral fertilizers sold in Germany.

    Science.gov (United States)

    Kratz, Sylvia; Schick, Judith; Schnug, Ewald

    2016-01-15

    68 rock phosphates and 162 P containing (organo-)mineral fertilizers sold in Germany were evaluated with regard to trace element contents. While Al, As, B, Be, Cd, Cr, Mo, Ni, Pb, Sb, Se, Tl, U, and Zn were higher in sedimentary than in igneous rock phosphates, the opposite was true for Co, Cu, Sn, Mn, Ti, Fe, and Sr. Comparing element concentrations to the currently valid legal limit values defined by the German Fertilizer Ordinance, it was found that some PK and many straight P fertilizers (superphosphate, triple superphosphate, partly acidulated rock phosphates) exceeded the limit of 50 mg Cd/kg P2O5. Mean values for As, Ni, Pb, and Tl remained below legal limits in almost all cases. While no legal limit has been defined for U in Germany yet, the limit of 50 mg U/kg P2O5 for P containing fertilizers proposed by the German Commission for the Protection of Soils was clearly exceeded by mean values for all fertilizer types analyzed. A large share of the samples evaluated in this work contained essential trace elements at high concentrations, with many of them not being declared as such. Furthermore, trace elements supplied with these fertilizers at a fertilization rate leveling P uptake would exceed trace element uptake by crops. This may become most relevant for B and Fe, since many crops are sensitive to an oversupply of B, and Fe loads exceeding plant uptake may immobilize P supplies for the crops by forming Fe phosphate salts. The sample set included two products made from thermochemically treated sewage sludge ash. The products displayed very high concentrations of Fe and Mn and exceeded the legal limit for Ni, emphasizing the necessity to continue research on heavy metal removal from recycled raw materials and the development of environmentally friendly and agriculturally efficient fertilizer products.

  5. Preparation of porous chitosan-poly(acrylic acid)-calcium phosphate hybrid nanoparticles via mineralization

    Institute of Scientific and Technical Information of China (English)

    CHEN ChangJing; DENG Yu; YAN ErYun; HU Yong; JIANG XiQun

    2009-01-01

    In this work,the preparation of chitosan-poly(acrylic acid)-calcium phosphate hybrid nanoparticles (CS-PAA-CaP NP) based on the mineralization of calcium phosphate (CAP) on the surface of chitosan-poly (acrylic acid) nanoparticles (CS-PAA NPs) was reported. CS-PAA-CaP NPs were achieved by directly adding ammonia to the aqueous solution of CS-PAA nanoparticles or by thermal decomposition of urea in the aqueous solution of CS-PAA nanoparticles,resulting in the mineralization of CaP on the surface of CS-PAA NPs. Through these two routes,especially using urea as a pH-regulator,the precipitation of CS-PAA NPs,a common occurrence in basic environment,was avoided. The size,morphology and ingredient of CS-PAA-CaP hybrid nanoparticles were characterized by dynamic light scattering (DLS),transmission electron microscope (TEM),scanning electron microscope (SEM),thermogravimetry analysis (TGA) and X-ray diffractometer (XRD). When urea was used as the pH regulator to facilitate the mineralization during the thermal urea decomposition procedure,regular CS-PAA-CaP hybrid nanoparticles with a porosity-structural CaP shells and 400-600 nm size were obtained. TGA result revealed that the hybrid NPs contained approximately 23% inorganic component,which was consistent with the ratio of starting materials. The XRD spectra of hybrid nanoparticles indicated that dicalcium phosphate (DCP:CaHPO4) crystal was a dominant component of mineralization.The porous structure of the CS-PAA-CaP hybrid NPs might be greatly useful in pharmaceutical and other medical applications.

  6. Plasma electrolytic oxidation of titanium in a phosphate/silicate electrolyte and tribological performance of the coatings

    Energy Technology Data Exchange (ETDEWEB)

    Aliasghari, S.; Skeldon, P., E-mail: p.skeldon@manchester.ac.uk; Thompson, G.E.

    2014-10-15

    Highlights: • Plasma electrolytic oxidation performed of titanium in silicate/phosphate electrolyte. • Range of duty cycle, current density, positive-to-negative current ratio studied. • Coatings contain anatase, rutile, Ti{sub 3}O{sub 5}, and amorphous silica. • Ptfe incorporated into coatings by addition of ptfe emulsion to the electrolyte. • Fiction reduced but wear life relatively short due to porosity of coatings. - Abstract: Plasma electrolytic oxidation of titanium has been investigated using a phosphate/silicate electrolyte with a square waveform and a frequency of 50 Hz. A range of constant rms current densities, duty cycles and negative-to-positive current ratios was employed. The resultant coatings were examined by analytical scanning and transmission electron microscopies and X-ray diffraction. The coatings, which were limited in thickness to ∼40 to 50 μm, contained anatase, rutile, Ti{sub 2}O{sub 5} and silicon-rich, amorphous material. The tribological behaviour was investigated using a ball-on-disc test, revealing a coefficient of friction against steel of ∼0.8, which reduced to ∼0.4 by incorporation of ptfe particles from the electrolyte. However, due to the composition and morphology of the coatings, their wear life was relatively short.

  7. Differential effects of zinc and magnesium ions on mineralization activity of phosphatidylserine calcium phosphate complexes.

    Science.gov (United States)

    Wu, Licia N Y; Genge, Brian R; Wuthier, Roy E

    2009-07-01

    Mg(2+) and Zn(2+) are present in the mineral of matrix vesicles (MVs) and biological apatites, and are known to influence the onset and progression of mineral formation by amorphous calcium phosphate (ACP) and hydroxyapatite (HAP). However, neither has been studied systematically for its effect on mineral formation by phosphatidylserine-Ca(2+)-Pi complexes (PS-CPLX), an important constituent of the MV nucleation core. Presented here are studies on the effects of increasing levels of Mg(2+) and Zn(2+) on the process of mineral formation, either when present in synthetic cartilage lymph (SCL), or when incorporated during the formation of PS-CPLX. Pure HAP and PS-CPLX proved to be powerful nucleators, but ACP took much longer to induce mineral formation. In SCL, Mg(2+) and Zn(2+) had significantly different inhibitory effects on the onset and amount of mineral formation; HAP and PS-CPLX were less affected than ACP. Mg(2+) and Zn(2+) caused similar reductions in the rate and length of rapid mineral formation, but Zn(2+) was a more potent inhibitor on a molar basis. When incorporated into PS-CPLX, Mg(2+) and Zn(2+) caused significantly different effects than when present in SCL. Even low, subphysiological levels of Mg(2+) altered the inherent structure of PS-CPLX and markedly reduced its ability to induce and propagate mineral formation. Incorporated Zn(2+) caused significantly less effect, low (<20 microM) levels causing almost no inhibition. Levels of Zn(2+) present in MVs do not appear to inhibit their nucleational activity.

  8. Aluminium phosphate and phosphate-sulphate minerals in kyanite schists of the Ichetuyskoye area, West Transbaikalia, Russia: crystal chemistry and evolution

    Science.gov (United States)

    Izbrodin, Ivan A.; Ripp, German S.; Doroshkevich, Anna G.

    2011-01-01

    Aluminium phosphate and aluminium phosphate-sulphate (APS) minerals occur as disseminated crystals and fine-grained aggregates in kyanite schists near Ichetuyskoye, in the Dzhida basin (West Transbaikal region, Russia). Petrographical, mineralogical and geochemical data suggest a metamorphic evolution through prograde and retrograde stages. Lazulite-scorzalite and trolleite in association with kyanite, quartz, muscovite, paragonite, topaz, rutile, magnetite and hematite formed during the prograde stage. More than 25 minerals identified in schists are genetically related to the retrograde stage. Some phosphates and all of the APS minerals belong to the alunite, beudantite and plumbogummite groups. Electron-microprobe data reveal the presence of wide compositional variations and complex solid-solution series among the members. The main crystal-chemical variations of the APS solid-solution series in the alunite supergroup concern the relative proportions of svanbergite, woodhouseite, goyazite, crandallite, florencite-(Ce) and natroalunite. Chemical analyses of APS minerals indicate extremely high amounts of LREE, Sr, Ba, Ca and Na. In some cases, APS minerals have compositions of Ba and Ca,Ba phosphates- sulphates.

  9. NELL-1 increases pre-osteoblast mineralization using both phosphate transporter Pit1 and Pit2

    Energy Technology Data Exchange (ETDEWEB)

    Cowan, Catherine M. [Department of Bioengineering, University of California, Los Angeles, 420 Westwood Plaza,7523 Boelter Hall, Los Angeles, CA 90095 (United States); Dental and Craniofacial Research Institute and Section of Orthodontics, School of Dentistry, University of California, Los Angeles, 40833 Le Conte Ave, Los Angeles, CA 90095 (United States); Zhang, Xinli; James, Aaron W.; Mari Kim, T.; Sun, Nichole [Dental and Craniofacial Research Institute and Section of Orthodontics, School of Dentistry, University of California, Los Angeles, 40833 Le Conte Ave, Los Angeles, CA 90095 (United States); Wu, Benjamin [Department of Bioengineering, University of California, Los Angeles, 420 Westwood Plaza,7523 Boelter Hall, Los Angeles, CA 90095 (United States); Dental and Craniofacial Research Institute and Section of Orthodontics, School of Dentistry, University of California, Los Angeles, 40833 Le Conte Ave, Los Angeles, CA 90095 (United States); Ting, Kang [Dental and Craniofacial Research Institute and Section of Orthodontics, School of Dentistry, University of California, Los Angeles, 40833 Le Conte Ave, Los Angeles, CA 90095 (United States); Soo, Chia, E-mail: bsoo@ucla.edu [UCLA and Orthopaedic Hospital Department of Orthopaedic Surgery and the Orthopaedic, Hospital Research Center, University of California, Los Angeles, 2641 Charles E. Young Dr. South, Los Angeles, CA 90095 (United States)

    2012-06-08

    Highlights: Black-Right-Pointing-Pointer NELL-1 accelerates extracellular matrix mineralization in MC3T3-E1 pre-osteoblasts. Black-Right-Pointing-Pointer NELL-1 significantly increases intracellular inorganic phosphate levels. Black-Right-Pointing-Pointer NELL-1 positively regulates osteogenesis but not proliferation in MC3T3-E1 cells. Black-Right-Pointing-Pointer NELL-1 regulates inorganic phosphate transporter activity. -- Abstract: NELL-1 is a potent osteoinductive molecule that enhances bone formation in multiple animal models through currently unidentified pathways. In the present manuscript, we hypothesized that NELL-1 may regulate osteogenic differentiation accompanied by alteration of inorganic phosphate (Pi) entry into the osteoblast via sodium dependent phosphate (NaPi) transporters. To determine this, MC3T3-E1 pre-osteoblasts were cultured in the presence of recombinant human (rh)NELL-1 or rhBMP-2. Analysis was performed for intracellular Pi levels through malachite green staining, Pit-1 and Pit-2 expression, and forced upregulation of Pit-1 and Pit-2. Results showed rhNELL-1 to increase MC3T3-E1 matrix mineralization and Pi influx associated with activation of both Pit-1 and Pit-2 channels, with significantly increased Pit-2 production. In contrast, Pi transport elicited by rhBMP-2 showed to be associated with increased Pit-1 production only. Next, neutralizing antibodies against Pit-1 and Pit-2 completely abrogated the Pi influx effect of rhNELL-1, suggesting rhNELL-1 is dependent on both transporters. These results identify one potential mechanism of action for rhNELL-1 induced osteogenesis and highlight a fundamental difference between NELL-1 and BMP-2 signaling.

  10. Electrochemical behavior of near-beta titanium biomedical alloys in phosphate buffer saline solution.

    Science.gov (United States)

    Dalmau, A; Guiñón Pina, V; Devesa, F; Amigó, V; Igual Muñoz, A

    2015-03-01

    The electrochemical behavior of three different near-β titanium alloys (composed by Ti, Nb and Sn) obtained by powder metallurgy for biomedical applications has been investigated. Different electrochemical and microscopy techniques were used to study the influence of the chemical composition (Sn content) and the applied potential on the microstructure and the corrosion mechanisms of those titanium alloys. The addition of Sn below 4wt.% to the titanium powder improves the microstructural homogeneity and generates an alloy with high corrosion resistance with low elastic modulus, being more suitable as a biomaterial. When the Sn content is above 4%, the corrosion resistance considerably decreases by increasing the passive dissolution rate; this effect is enhanced with the applied potential.

  11. Tribocorrosion behavior of beta titanium biomedical alloys in phosphate buffer saline solution.

    Science.gov (United States)

    Pina, V Guiñón; Dalmau, A; Devesa, F; Amigó, V; Muñoz, A Igual

    2015-06-01

    The tribo-electrochemical behavior of different β titanium alloys for biomedical applications sintered by powder metallurgy has been investigated. Different mechanical, electrochemical and optical techniques were used to study the influence of the chemical composition, Sn content, and the electrochemical conditions on the tribocorrosion behavior of those alloys Ti30NbxSn alloys (where "x" is the weight percentage of Sn content, 2% and 4%). Sn content increases the active and passive dissolution rate of the titanium alloys, thus increasing the mechanically activated corrosion under tribocorrosion conditions. It also increases the mechanical wear of the alloy. Prevailing electrochemical conditions between -1 and 2V influences the wear accelerated corrosion by increasing it with the applied potential and slightly increases the mechanical wear of Ti30Nb4Sn. Wear accelerated corrosion can be predicted by existing models as a function of electrochemical and mechanical parameters of the titanium alloys.

  12. Porous titania surfaces on titanium with hierarchical macro- and mesoporosities for enhancing cell adhesion, proliferation and mineralization

    Energy Technology Data Exchange (ETDEWEB)

    Han, Guang [Department of Materials and Environmental Chemistry, Arrhenius Laboratory, Stockholm University, 10691 Stockholm (Sweden); Müller, Werner E.G.; Wang, Xiaohong [ERC Advanced Grant Research Group at the Institute for Physiological Chemistry, University Medical Center of the Johannes Gutenberg University Mainz, Duesbergweg 6, D-55128 Mainz (Germany); Lilja, Louise [Department of Materials and Environmental Chemistry, Arrhenius Laboratory, Stockholm University, 10691 Stockholm (Sweden); Department of Physics, Chemistry and Biology, Linköping University, SE-581 83 Linköping (Sweden); Shen, Zhijian, E-mail: shen@mmk.su.se [Department of Materials and Environmental Chemistry, Arrhenius Laboratory, Stockholm University, 10691 Stockholm (Sweden)

    2015-02-01

    Titanium received a macroporous titania surface layer by anodization, which contains open pores with average pore diameter around 5 μm. An additional mesoporous titania top layer following the contour of the macropores, of 100–200 nm thickness and with a pore diameter of 10 nm, was formed by using the evaporation-induced self-assembly (EISA) method with titanium (IV) tetraethoxide as the precursor. A coherent laminar titania surface layer was thus obtained, creating a hierarchical macro- and mesoporous surface that was characterized by high-resolution electron microscopy. The interfacial bonding between the surface layers and the titanium matrix was characterized by the scratch test that confirmed a stable and strong bonding of titania surface layers on titanium. The wettability to water and the effects on the osteosarcoma cell line (SaOS-2) proliferation and mineralization of the formed titania surface layers were studied systematically by cell culture and scanning electron microscopy. The results proved that the porous titania surface with hierarchical macro- and mesoporosities was hydrophilic that significantly promoted cell attachment and spreading. A synergistic role of the hierarchical macro- and mesoporosities was revealed in terms of enhancing cell adhesion, proliferation and mineralization, compared with the titania surface with solo scale topography. - Highlights: • We developed a hierarchical macro- and mesoporous surface layer on titanium. • New surface layer was strong enough to sustain on implant surface. • New surface owned better surface wettability. • New surface can promote SaOS-2 cell adhesion, proliferation and mineralization. • Synergistic effects on cell responses occur when two porous structures coexist.

  13. Thermal cycling effect of dicalcium phosphate-reinforced composites on auto-mineralized dental resin.

    Science.gov (United States)

    Chen, Wen-Cheng; Chang, Kai-Chi; Wu, Hui-Yu; Ko, Chia-Ling; Huang, Chien-Lin

    2014-12-01

    The mineralizing capabilities of surface-modified dicalcium phosphate anhydrous (DCPA), reinforced and treated with nanocrystals and capped with silane, in composite resins were analyzed via thermal cycling. We compared two light-curable composites that were mixed at filler-to-resin mass ratios of 30/70 and 50/50. The strengths, elastic moduli, and topographical structures of the samples were determined after thermal cycling between 5 and 55°C in deionized water for 600 and 2400 cycles. Silane-capped particles decreased the strength but enhanced the mineralizing capability of the composites. Nanocrystal-treated filler surfaces significantly increased the strength and moduli of the composites after 600 thermal cycles. However, these values declined after 2400 thermal cycles. The nanocrystal-treated filler surfaces prevented the reduction in strength before and after 2400 thermal cycles. Prior to silane capping, the nanocrystal-treated DCPA filler surfaces exhibited good mineralization capability without compromising strength. The potential for barrier generation through mineralization yielded positive effects and prevented micro-leakages. Copyright © 2014 Elsevier B.V. All rights reserved.

  14. Isolation and characterization of biogenic calcium carbonate/phosphate from oral bacteria and their adhesion studies on YSZ-coated titanium substrate for dental implant application

    Indian Academy of Sciences (India)

    GOBI SARAVANAN KALIARAJ; KAMALAN KIRUBAHARAN; G PRADHABAN; P KUPPUSAMI; VINITA VISHWAKARMA

    2016-04-01

    Biogenic calcium carbonate/phosphate were isolated and characterized from oral bacteria (CPOB). The crystalline nature and morphology of calcium carbonate/phosphate were characterized by X-ray diffraction (XRD)and field emission scanning electron microscopy (FESEM), respectively. XRD analysis revealed the cubic phase of YSZ coating as well as biogenic calcium carbonate (rhombohedral) and calcium phosphate oxide (hexagonal) wasobserved from CPOB. FESEM confirmed the extracellular synthesis of calcium compounds. Bacterial adhesion result reveals that YSZ coating drastically reduce bacterial invasion than titanium substrate.

  15. Artificial citrate operon confers mineral phosphate solubilization ability to diverse fluorescent pseudomonads.

    Directory of Open Access Journals (Sweden)

    Hemanta Adhikary

    Full Text Available Citric acid is a strong acid with good cation chelating ability and can be very efficient in solubilizing mineral phosphates. Only a few phosphate solubilizing bacteria and fungi are known to secrete citric acids. In this work, we incorporated artificial citrate operon containing NADH insensitive citrate synthase (gltA1 and citrate transporter (citC genes into the genome of six-plant growth promoting P. fluorescens strains viz., PfO-1, Pf5, CHAO1, P109, ATCC13525 and Fp315 using MiniTn7 transposon gene delivery system. Comprehensive biochemical characterization of the genomic integrants and their comparison with plasmid transformants of the same operon in M9 minimal medium reveals the highest amount of ∼7.6±0.41 mM citric and 29.95±2.8 mM gluconic acid secretion along with ∼43.2±3.24 mM intracellular citrate without affecting the growth of these P. fluorescens strains. All genomic integrants showed enhanced citric and gluconic acid secretion on Tris-Cl rock phosphate (TRP buffered medium, which was sufficient to release 200-1000 µM Pi in TRP medium. This study demonstrates that MPS ability could be achieved in natural fluorescent pseudomonads by incorporation of artificial citrate operon not only as plasmid but also by genomic integration.

  16. Mineral Phosphate Solubilizing Bacteria Isolated from Various Plant Rhizosphere under Different Aluminum Content

    Directory of Open Access Journals (Sweden)

    Dolly Iriani Damarjaya

    2015-10-01

    Full Text Available The objectives of this study was to isolate and characterize the mineral phosphate solubilizing bacteriafrom rhizosphere and evaluate their potential as plant growth promoting bacteria in Al-toxic soils. The halozone formation method was used to isolate PSB using the media containing insoluble phosphates (Ca-P or Al-Pas a source of phosphate. Eight of acid and Al-tolerant PSB isolates that were able to solubilize Ca-P wereobtained from rhizosphere of clover, wheat, corn, and sunflower grown in Al-toxic soil. Identification of theisolates based on the 16S rRNA gene sequence analysis demonstrated that the isolates were strains of Burkholderia(5 strains, Pseudomonas (1 strain, Ralstonia (1 strain, and unidentified bacterium (1 strains. All PSB isolatesshowed the capability to dissolve Ca-P, and only 1 strain (Ralstonia strain was able to dissolve Al-P in agar platemedium. The P-solubilization by these isolates was correlated with pH of medium. Inoculation of the bacterialstrains on clover on Al-toxic medium showed that all isolates increased the plant dry weight compared withuninoculated treatment. Our results showed that those PSB isolates have potential to be developed as a biofertilizerto increase the efficiency of P-inorganic fertilizer used in Al-toxic soils.

  17. Artificial citrate operon confers mineral phosphate solubilization ability to diverse fluorescent pseudomonads.

    Science.gov (United States)

    Adhikary, Hemanta; Sanghavi, Paulomi B; Macwan, Silviya R; Archana, Gattupalli; Naresh Kumar, G

    2014-01-01

    Citric acid is a strong acid with good cation chelating ability and can be very efficient in solubilizing mineral phosphates. Only a few phosphate solubilizing bacteria and fungi are known to secrete citric acids. In this work, we incorporated artificial citrate operon containing NADH insensitive citrate synthase (gltA1) and citrate transporter (citC) genes into the genome of six-plant growth promoting P. fluorescens strains viz., PfO-1, Pf5, CHAO1, P109, ATCC13525 and Fp315 using MiniTn7 transposon gene delivery system. Comprehensive biochemical characterization of the genomic integrants and their comparison with plasmid transformants of the same operon in M9 minimal medium reveals the highest amount of ∼7.6±0.41 mM citric and 29.95±2.8 mM gluconic acid secretion along with ∼43.2±3.24 mM intracellular citrate without affecting the growth of these P. fluorescens strains. All genomic integrants showed enhanced citric and gluconic acid secretion on Tris-Cl rock phosphate (TRP) buffered medium, which was sufficient to release 200-1000 µM Pi in TRP medium. This study demonstrates that MPS ability could be achieved in natural fluorescent pseudomonads by incorporation of artificial citrate operon not only as plasmid but also by genomic integration.

  18. The new hybrid ceramic beads synthesized from natural minerals and titanium dioxide for the waste water cleaning

    OpenAIRE

    SATA, Akiyoshi; Hirose, Masanao; Kurawaki, Junichi; "KUSUMOTO, Yoshifumi"; HAYAKAWA, Katumitu

    2006-01-01

    Porous hybrid ceramic beads were synthesized by burning at 1090°C under a reductive atmosphere. They consist of the natural mineral (graphite silica, GS), the pyroclastic deposit “shirasu” and titanium dioxide. They showed the bleaching of the aqueous dyestuff solutions (rhodamin B, acridine orange, methyl orange, methylene blue) and the degradation of a surfactant dodecyltrimethylpyridinium bromide and humic acid. The decolorizing rate of dye stuff was monitored by the absorpt...

  19. Osteogenicity of titanium implants coated with calcium phosphate or collagen type-I in osteoporotic rats

    NARCIS (Netherlands)

    Alghamdi, H.S.A.; Bosco, R.; Beucken, J.J. van den; Walboomers, X.F.; Jansen, J.A.

    2013-01-01

    This study hypothesized that modification of titanium implant surface, e.g. by the deposition of inorganic/organic coatings, can significantly improve the implant-bone response compared in osteoporotic vs. healthy conditions. After osteoporosis was induced in 15 female Wistar rats by ovariectomy

  20. Influence of sterilization on the mineralization of titanium implants induced by incubation in various biological model fluids.

    Science.gov (United States)

    Serro, A P; Saramago, B

    2003-11-01

    The aim of this work was to investigate the effect of the sterilization processes on the mineralization of titanium implants induced by incubation in various biological model fluids. Titanium samples were submitted to the following sterilization processes used for implant materials: steam autoclaving, glow discharge Ar plasma treatment and gamma-irradiation. The modification of the treated surfaces was evaluated by contact angle determinations, X-ray photoelectron spectroscopy (XPS), laser profilometry and X-ray diffraction. The most significant modifications were detected on the wettability: while the samples treated with Ar plasma became highly hydrophilic (water contact angle approximately 0 degrees), gamma-irradiation and steam sterilization induced an increase in the hydrophobicity. After being sterilized, the samples were incubated for one week in three biological model fluids: Hanks' Balanced Salt Solution, Kokubo's simulated body fluid (SBF) and a fluid, designated by SBF0, with the same composition of SBF but without buffer TRIS. The level of mineralization of the incubated Ti samples, assessed by dynamic contact angle analysis, scanning electron microscopy, electron dispersive spectroscopy and XPS, indicated that the early stages of mineralization are essentially independent of the sterilization method. In contrast, the incubating fluid plays a determinant role, SBFO being the most efficient medium for biomineralization of titanium.

  1. 3D Geologic Modeling. The example of the Farim-Saliquinhé Phosphates Mineralization.

    Science.gov (United States)

    Ferreira, António; Charifo, Gilberto; Almeida, José

    2010-05-01

    The construction of three-dimensional geologic models representing both the structure and properties inherent to each geological unit is nowadays possible due to the computational development of the last decades. The 3D Geologic Modeling (3DGM) is very efficient for storage, display and transfer of geoscience information, and is a key tool in the oil industry in particular for the reservoir characterization and modeling; its use in other geosciences areas has been growing in recent years but is still scarce. In the present work we show a 3D geologic model of the phosphates mineralization of Farim-Saliquinhé (Guinea-Bissau) as a first example of the work being developed in the research center CICEGe (FCT-UNL) by its novel research group on 3DGM, and to demonstrate the usefulness of this kind of geologic models, built with appropriate software, in order to better represent, study, characterize and visualize a geologic case study. The phosphates mineralization of Farim-Saliquinhé (Guinea-Bissau) is a sedimentary deposit located near Saliquinhé, Farim and the Rio Cachéu. The deposit is composed by two members: 1) FPB, an early Middle to Upper Lutetian calcareous-phosphate member; 2) FPA, an upper member of descarbonatized phosphate. Micritic limestones are underlying the mineralized layers, while dolomitic limestones, the FPO phosphate interval, and a younger sandy clayey cover are overlying the phosphatic members (BRGM, 1983; Prian et al., 1987). This work is based on geologic and geochemical data from 69 vertical boreholes carried out by BRGM in the 80s (completed with topographic data). This survey covered an area of about 10x5 km and was aimed to determine the geometry and the reserves of the FPA and FPB phosphate mineralization. The 3D geologic model was developed in gOcad software, which uses a distinctive interpolation method to build the geometry of objects, the DSI - discrete smooth interpolation. The 3D geologic model was built on the BRGM's study area

  2. Promoting Effect of Layered Titanium Phosphate on the Electrochemical and Photovoltaic Performance of Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Deng Changsheng

    2010-01-01

    Full Text Available Abstract We reported a composite electrolyte prepared by incorporating layered α-titanium phosphate (α-TiP into an iodide-based electrolyte using 1-ethyl-3-methylimidazolium tetrafluoroborate(EmimBF4 ionic liquid as solvent. The obtained composite electrolyte exhibited excellent electrochemical and photovoltaic properties compared to pure ionic liquid electrolyte. Both the diffusion coefficient of triiodide (I3 − in the electrolyte and the charge-transfer reaction at the electrode/electrolyte interface were improved markedly. The mechanism for the enhanced electrochemical properties of the composite electrolyte was discussed. The highest conversion efficiency of dye-sensitized solar cell (DSSC was obtained for the composite electrolyte containing 1wt% α-TiP, with an improvement of 58% in the conversion efficiency than the blank one, which offered a broad prospect for the fabrication of stable DSSCs with a high conversion efficiency.

  3. Reflections on the Mechanism of Calcium Phosphate Nucleation on Titanium in Simulated Body Fluids

    Institute of Scientific and Technical Information of China (English)

    F. T. Cheng

    2005-01-01

    The results and main findings of studies reported in the literature in relation to the deposition of calcium phosphate on Ti in simulated body fluids are summarized. The effects of the surface hydroxyl groups and the sign of surface charge on the nucleation of calcium phosphate are reviewed. One major controversy among the conclusions of different studies is the order of adsorption of the calcium ions and the phosphate ions in the initial stage of immersion. A simple model based on the amphoteric nature of the hydroxyl groups on Ti is proposed in an attempt to delineate the nucleation process for calcium phosphate on Ti in simulated body fluids. HPO42- ions interact with the hydroxyl groups via ion exchange and/or electrostatic attraction, and Ca2+ ions, via electrostatic attraction only. There is no preferential order of adsorption. Seemingly inconsistent results in different studies possibly arise from different prior treatments of the samples, which affect the adsorption properties.

  4. Vibrational spectroscopic study of the phosphate mineral kryzhanovskite and in comparison with reddingite-implications for the molecular structure

    Science.gov (United States)

    Frost, Ray L.; Scholz, Ricardo; Wang, Lina

    2016-08-01

    We have studied the phosphate mineral kryzhanovskite (Fe3+,Mn2+)3(PO4)2(OH,H2O) which is a member of the phosphoferrite mineral group using a combination of scanning electron microscopy with energy dispersive spectroscopy and Raman and infrared spectroscopy. Chemical analysis shows the presence of P, Mn and Fe and confirms the formula given above. The presence of hydroxyl units in the structure is indicative of ferric iron in the formula that is an oxidised product. Raman spectroscopy coupled with infrared spectroscopy supports the concept of phosphate, hydrogen phosphate and dihydrogen phosphate units in the structure of kryzhanovskite -phosphoferrite. Infrared and Raman bands attributed to water and hydroxyl stretching modes are identified. Vibrational spectroscopy adds useful information to the molecular structure of kryzhanovskite -phosphoferrite.

  5. Titanium

    DEFF Research Database (Denmark)

    Fage, Simon W; Muris, Joris; Jakobsen, Stig S

    2016-01-01

    Exposure to titanium (Ti) from implants and from personal care products as nanoparticles (NPs) is common. This article reviews exposure sources, ion release, skin penetration, allergenic effects, and diagnostic possibilities. We conclude that human exposure to Ti mainly derives from dental...... and medical implants, personal care products, and foods. Despite being considered to be highly biocompatible relative to other metals, Ti is released in the presence of biological fluids and tissue, especially under certain circumstances, which seem to be more likely with regard to dental implants. Although...... most of the studies reviewed have important limitations, Ti seems not to penetrate a competent skin barrier, either as pure Ti, alloy, or as Ti oxide NPs. However, there are some indications of Ti penetration through the oral mucosa. We conclude that patch testing with the available Ti preparations...

  6. Novel phosphate-grafted ePTFE copolymers for optimum in vitro mineralization

    Energy Technology Data Exchange (ETDEWEB)

    Wentrup-Byrne, Edeline; Suzuki, Shuko; Groendahl, Lisbeth [Tissue Repair and Regeneration Program, Institute of Health and Biomedical Innovation, Queensland University of Technology, 60 Musk Avenue, Kelvin Grove, QLD 4059 (Australia); Suwanasilp, Juthakarn Jessica, E-mail: l.grondahl@uq.edu.a [School of Chemistry and Molecular Biosciences, University of Queensland, Cooper Rd, St Lucia, QLD 4072 (Australia)

    2010-08-01

    Surface modification via graft copolymerization is an attractive method for optimizing polymers used in biomedical applications. We developed a novel method using a mixed solvent system (either water and dichloromethane (DCM) or water, methanol and DCM) consisting of two solvent phases for grafting 2-(methacryloyloxy)ethyl phosphate onto expanded polytetrafluoroethylene (ePTFE). This new method resulted in the fabrication of grafted membranes with greater grafting extents (GEs) (as evaluated from x-ray photoelectron spectroscopy (XPS)) in the organic phase than those obtained when grafting was carried out in a single phase. It also made it possible to graft in the aqueous phase, a process that is otherwise inhibited by the concomitant formation of large amounts of highly crystalline homopolymer. Thorough characterization of the grafted membranes using gravimetric, XPS and attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) not only permitted evaluation of the grafting outcomes but also made it possible to analyze their dependence on monomer concentration and solvent composition. A selection of membranes was tested for their in vitro mineralization capacity using simulated body fluid. It was found that an 'ideal' mineralization outcome, i.e. a uniform coating of carbonated hydroxyapatite (cHAP) formed on the sample grafted in the aqueous phase of the water/DCM two-phase solvent system. A detailed discussion bringing together these results, as well as results from a series of earlier studies, allows conclusions regarding polymer chemistry and the topology necessary for cHAP mineralization.

  7. The development and characterization of a primarily mineral calcium phosphate - poly(epsilon-caprolactone) biocomposite

    Science.gov (United States)

    Dunkley, Ian Robert

    Orthopaedic reconstruction often involves the surgical introduction of structural implants that provide for rigid fixation, skeletal stabilization, and bone integration. The high stresses incurred by these implanted devices have historically limited material choices to metallic and select polymeric formulations. While mechanical requirements are achieved, these non-degradable materials do not participate actively in the remodeling of the skeleton and present the possibility of long-term failure or rejection. This is particularly relevant in cervical fusion, an orthopaedic procedure to treat damaged, degenerative or diseased intervertebral discs. A significant improvement on the available synthetic bone replacement/regeneration options for implants to treat these conditions in the cervical spine may be achieved with the development of primarily mineral biocomposites comprised of a bioactive ceramic matrix reinforced with a biodegradable polymer. Such a biocomposite may be engineered to possess the clinically required mechanical properties of a particular application, while maintaining the ability to be remodeled completely by the body. A biocomposite of Si-doped calcium phosphate (Si-CaP) and poly(epsilon-caprolactone) (PCL) was developed for application as such a synthetic bone material for potential use as a fusion device in the cervical spine. In this thesis, a method by which high mineral content Si-CaP/PCL biocomposites with interpenetrating matrices of mineral and polymer phases may be prepared will be demonstrated, in addition to the effects of the various preparation parameters on the biocomposite density, porosity and mechanical properties. This new technique by which dense, primarily ceramic Si-CaP/PCL biocomposites were prepared, allowed for the incorporation of mineral contents ranging between 45-97vol%. Polymer infiltration, accomplished solely by passive capillary uptake over several days, was found to be capable of fully infiltrating the microporosity

  8. Mineralization of annexin-5-containing lipid-calcium-phosphate complexes: modulation by varying lipid composition and incubation with cartilage collagens.

    Science.gov (United States)

    Genge, Brian R; Wu, Licia N Y; Wuthier, Roy E

    2008-04-11

    Matrix vesicles (MVs) in the growth plate bind to cartilage collagens and initiate mineralization of the extracellular matrix. Native MVs have been shown to contain a nucleational core responsible for mineral formation that is comprised of Mg(2+)-containing amorphous calcium phosphate and lipid-calcium-phosphate complexes (CPLXs) and the lipid-dependent Ca(2+)-binding proteins, especially annexin-5 (Anx-5), which greatly enhances mineral formation. Incorporation of non-Ca(2+)-binding MV lipids impedes mineral formation by phosphatidylserine (PS)-CPLX. In this study, nucleators based on amorphous calcium phosphate (with or without Anx-5) were prepared with PS alone, PS + phosphatidylethanolamine (PE), or PS + PE and other MV lipids. These were incubated in synthetic cartilage lymph containing no collagen or containing type II or type X collagen. Dilution of PS with PE and other MV lipids progressively retarded nucleation. Incorporation of Anx-5 restored nucleational activity to the PS:PE CPLX; thus PS and Anx-5 proved to be critical for nucleation of mineral. Without Anx-5, induction of mineral formation was slow unless high levels of Ca(2+) were used. The presence of type II collagen in synthetic cartilage lymph improved both the rate and amount of mineral formation but did not enhance nucleation. This stimulatory effect required the presence of the nonhelical telopeptides. Although type X collagen slowed induction, it also increased the rate and amount of mineral formation. Both type II and X collagens markedly increased mineral formation by the MV-like CPLX, requiring Anx-5 to do so. Thus, Anx-5 enhances nucleation by the CPLXs and couples this to propagation of mineral formation by the cartilage collagens.

  9. Effects of sandblasting, H2SO4/HCl etching, and phosphate primer application on bond strength of veneering resin composite to commercially pure titanium grade 4

    OpenAIRE

    Egoshi, Takafumi; Taira, Yohsuke; Soeno, Kohyoh; SAWASE Takashi

    2013-01-01

    This study investigated the effects of surface treatments on the bond strength of a resin composite to a commercially pure titanium. The bonding surfaces of all titanium specimens were ground with 1,000-grit silicon carbide paper and then subjected to one or more of these surface treatments: sandblasting with alumina (sand), etching with 45wt% H2SO4 and 15wt% HCl (SH-etchant) at 70°C for 10 min, and/or phosphate primer (MDP-primer) application. Specimens not subjected to any surface treatment...

  10. Phosphovanadylite: a new vanadium phosphate mineral with a zeolite-type structure

    Science.gov (United States)

    Medrano, M.D.; Evans, H.T.; Wenk, H.-R.; Piper, D.Z.

    1998-01-01

    Phosphovanadylite, whose simplified formula is (Ba,Ca,K,Na)x([(Va,Al)4P2(P,OH)16].12H2), is a new vanadium phosphate zeolite mineral found in the Phosphoria Formation at Monsanto's Enoch Valley Mine, Soda Springs, Idaho. Its formula in more detail is (Ba0.38Ca0.20K0.006Na0.02)??0.66 [P2(V3.44Al0.046)??3.90O10.34(OH)5.66] .12H2O. The drusy mineral occurs as pale greenish-blue euhedral cubes (20-50 ??m edge) coating phosphatic, organic-rich mudstone. The chemical composition determined by electron microprobe is (in weight percent) V-28.02, P-9.91, Al-1.97, Ca-1.31, Ba-8.28, Cd-0.09, Zn-0.34, Na-0.15, K-0.73, O-46.57, and F-0.03. The index of refraction is nD = 1.566 (4) and specific gravity is 2.16 (3). The X-ray powder pattern shows strong reflections at 3.16 A (422), 2.58 (600), 2.44 (620), and 7.73 (200), which are indexed on the basis of a cubic body-centered unit cell with a = 15.470 (4) A. From the single-crystal structure analysis, its space group was determined to be I43m, Z = 6, and its structure consists of V4O18 16 octahedral clusters linked to each other by P atoms to form a cubic lattice, creating cavities 7.0 and 5.5 A in diameter where mainly H2O resides. Final residual indexes are R = 0.066, Rw = 0.061, goodness-of-fit = 0.75, and 93 observations and 24 parameters.

  11. Mineral phosphate solubilization by wild type and radiation induced mutants of pantoea dispersa and pantoea terrae

    Energy Technology Data Exchange (ETDEWEB)

    Murugesan, Senthilkumar; Lee, Young Keun; Kim, Jung Hun [Korea Atomic Energy Research Institte, Jeongeup (Korea, Republic of)

    2009-03-15

    Three mineral phosphate solubilizing (MPS) bacteria where isolated from rhizosphere soil samples of common bean and weed plants. 16S rDNA analysis indicated that the isolate P2 and P3 are closely related to Pantoea dispersa while isolate P4 is closely related to Pantoea terrae. Islates P2 and P3 recorded 381.60 {mu}g ml{sup -1} of tricalcium phosphate (TCP) solubilization respectively on 3 days incubation. Isolate P4 recorded the TCP solubilization of 215.85 {mu}g ml{sup -1} and the pH was dropped to 4.44 on 24 h incubation. Further incubation of P4 sharply decreased the available phosphorous to 28.94 {mu}g ml{sup -1} and pH level was raised to 6.32. Gamma radiation induced mutagenesis was carried out at LD{sub 99} dose of the wild type strains. The total of 14 mutant clones with enhanced MPS activity and 4 clones with decreased activity were selected based on solubilization index (SI) and phosphate solubilization assay. Mutant P2-M1 recorded the highest P-solubilizing potential among any other wild or mutnat clones by releasing 504.21 {mu}g ml{sup -1} of phosphorous i.e. 35% higher than its wild type by the end of day 5. A comparative evaluation of TCP solubilization by wild type isolates of Pantoea and their mutants, led to select three MPS mutant clones such as P2-M1, P3-M2 and P3-M4 with a potential to release >471.67 {mu}g ml{sup {sub {sup 1}}} of phosphorous from TCP. These over expressing mutant clones are considered as suitable candidates for biofertilization.

  12. Water-Soluble Cellulose Derivatives Are Sustainable Additives for Biomimetic Calcium Phosphate Mineralization

    Directory of Open Access Journals (Sweden)

    Andreas Taubert

    2016-10-01

    Full Text Available The effect of cellulose-based polyelectrolytes on biomimetic calcium phosphate mineralization is described. Three cellulose derivatives, a polyanion, a polycation, and a polyzwitterion were used as additives. Scanning electron microscopy, X-ray diffraction, IR and Raman spectroscopy show that, depending on the composition of the starting solution, hydroxyapatite or brushite precipitates form. Infrared and Raman spectroscopy also show that significant amounts of nitrate ions are incorporated in the precipitates. Energy dispersive X-ray spectroscopy shows that the Ca/P ratio varies throughout the samples and resembles that of other bioinspired calcium phosphate hybrid materials. Elemental analysis shows that the carbon (i.e., polymer contents reach 10% in some samples, clearly illustrating the formation of a true hybrid material. Overall, the data indicate that a higher polymer concentration in the reaction mixture favors the formation of polymer-enriched materials, while lower polymer concentrations or high precursor concentrations favor the formation of products that are closely related to the control samples precipitated in the absence of polymer. The results thus highlight the potential of (water-soluble cellulose derivatives for the synthesis and design of bioinspired and bio-based hybrid materials.

  13. Biotic and abiotic pathways of phosphorus cycling in minerals and sediments: insights from oxygen isotope ratios in phosphate.

    Science.gov (United States)

    Jaisi, Deb P; Kukkadapu, Ravi K; Stout, Lisa M; Varga, Tamas; Blake, Ruth E

    2011-08-01

    A key question to address in the development of oxygen isotope ratios in phosphate (δ(18)O(p)) as a tracer of biogeochemical cycling of phosphorus in ancient and modern environments is the nature of isotopic signatures associated with uptake and cycling of mineral-bound phosphate by microorganisms. Here, we present experimental results aimed at understanding the biotic and abiotic pathways of P cycling during biological uptake of phosphate sorbed to ferrihydrite and the selective uptake of sedimentary phosphate phases by Escherichia coli and Marinobacter aquaeolei. Results indicate that a significant fraction of ferrihydrite-bound phosphate is biologically available. The fraction of phosphate taken up by E. coli attained an equilibrium isotopic composition in a short time (isotope exchange (between O in PO(4) and O in water; that is, actual breaking and reforming of P-O bonds) (biotic pathway). The difference in isotopic composition between newly equilibrated aqueous and residual sorbed phosphate groups promoted the ion exchange (analogous to isotopic mixing) of intact phosphate ions (abiotic pathway) so that this difference gradually became negligible. In sediment containing different P phases, E. coli extracted loosely sorbed phosphate first, whereas M. aquaeolei preferred Fe-oxide-bound phosphate. The presence of bacteria always imprinted a biotic isotopic signature on the P phase that was taken up and cycled. For example, the δ(18)O(p) value of loosely sorbed phosphate shifted gradually toward equilibrium isotopic composition. The δ(18)O(p) value of Fe-oxide-bound phosphate, however, showed only slight changes initially but, when new Fe-oxides were formed, coprecipitated/occluded phosphate retained δ(18)O values of the aqueous phosphate at the time of formation of new Fe oxides. Concentrations and isotopic compositions of authigenic and detrital phosphates did not change, suggesting that these phosphate phases were not utilized by bacteria. These findings

  14. Pegmatito Gentil (Mendes Pimentel, MG e suas paragêneses mineralógicas de fosfatos raros Gentil Pegmatite (Mendes Pimentel, MG and their rare phosphate mineral assemblages

    Directory of Open Access Journals (Sweden)

    Mario Luiz de Sá C. Chaves

    2008-06-01

    Full Text Available Centenas de corpos pegmatíticos na região nordeste de Minas Gerais produzem minerais gemológicos e de coleção, muitos desses corpos possuindo afinidades com determinada espécie, grupo ou classe mineral. O Pegmatito Gentil em Mendes Pimentel, ora descrito, notabiliza-se por sua assembléia de minerais fosfáticos, a maior parte dos quais raros ou raríssimos na natureza. A associação mineral identificada inclui microclínio, quartzo, muscovita, almandina-espessartita, berilo e trifilita como fosfato primário, que foi alterado formando uma extensa paragênese de espécies secundárias. Entre essas, destacam-se brazilianita, frondelita, gormanita, huréaulita, lazulita, litiofilita, purpurita, reddingita, woodhouseíta, zanaziíta e, recentemente descrita nesse corpo, a matioliíta.Hundreds of pegmatitic bodies occur in the northern region of the State of Minas Gerais, several of these bodies producing gemologic and collection minerals. Such pegmatites are known by the mineral affinity with certain minerals species, groups or classes. The Gentil Pegmatite (Mendes Pimentel county is characterized by the phosphatic mineral assemblage, and some of these minerals are rare or very rare in nature. Primary species are microcline, quartz, muscovite, almandine-espessartine, beryl, and triphylite as the main phosphate that was altered to an extensive paragenesis of secondary phosphates. In this list are noted brazilianite, frondelite, gormanite, hureaulite, lazulite, lithiophilite, purpurite, reddingite, woodhouseite, zanaziite, and matioliite, a species recently described in the Gentil Pegmatite.

  15. Morphometric immunohistochemical examination of the inflammatory tissue reaction after implantation of calcium phosphate-coated titanium plates in rats.

    Science.gov (United States)

    Walschus, Uwe; Hoene, Andreas; Neumann, Hans-Georg; Wilhelm, Lutz; Lucke, Silke; Lüthen, Frank; Rychly, Joachim; Schlosser, Michael

    2009-02-01

    Calcium phosphate (CaP) preparations are established coatings for titanium-based medical implants used for bone reconstruction. However, biodegradation of the coating can result in microparticles that subsequently cause inflammatory reactions. The present study was therefore aimed at investigating the inflammatory response to two series of CaP-coated titanium plates: Ti-brushite (Ti-B) and Ti-hydroxyapatite (Ti-H) implants. Fifteen male LEW.1A rats received one plate of each series and a pellet (5 x 2 mm) of sol-gel derived silica/CaP (SCP implants) implanted into the back musculature. After 7, 14 and 28 days, five rats were killed and the implants were removed with the surrounding tissue. Quantitative immunohistochemistry was performed on frozen sections. Total monocytes/macrophages, tissue macrophages, T-cells, MHC-class-II-positive cells and proliferating cells were counted. For the Ti-B implants, the number of monocytes/macrophages remained constant while the other cell populations increased. In contrast, for the Ti-H implants the number of monocytes/macrophages decreased while the other cell populations remained constant. The SCP implants demonstrated degradation and scattering into smaller particles with an increase for all cell populations except the proliferating cells. Human mesenchymal stem cells demonstrated adherence and a flat morphology on Ti-B and Ti-H implants and no remarkable difference between both implants. Taken together, the in vivo data demonstrate that the short-term inflammatory response against a hydroxyapatite coating is lower in comparison to a brushite coating, and that the morphology of cells growing in vitro is similar on both layers.

  16. Increasing potassium (K release from K-containing minerals in the presence of insoluble phosphate by bacteria

    Directory of Open Access Journals (Sweden)

    Mohammad Reza Sarikhani

    2016-03-01

    Full Text Available Introduction: Phosphorus and potassium are major essential macronutrients for biological growth and development. Application of soil microorganisms is one approach to enhance crop growth. Some bacteria are efficient in releasing K and solubilizing P from mineral sources but their behavior was not studied more in presence together. Materials and methods: In this study the ability of seven bacterial strains, including Pseudomonas putida P13, P. putida Tabriz, P. fluorescens Tabriz, P. fluorescens Chao, Pantoea agglomerans P5, Azotobacter sp. and Bacillus megaterium JK3 to release mineral K from muscovite and biotite with application of insoluble (Ca3(PO42 or soluble (Na2HPO4 P-sources was investigated. Nutrient Broth was used to prepare an overnight culture of bacteria to inoculate in Aleksandrov medium, which was used to study the dissolution of silicate minerals. It should be mentioned that Aleksandrov medium was used to determine the amount of released P from tricalcium phosphate (TCP while muscovite was added to the medium as a sole source of potassium. Concentration of P was determined spectrophotometrically by ammonium-vanadate-molybdate method and K was determined by flame photometry. Results: The insoluble P-source led to a significantly increased released K into assay medium (66%, and the net release of K from the biotite was significantly enhanced. Among bacterial strains, the highest mean of released K was observed with P. putida P13 which released more K (27% than the control. The amounts of released K from micas in the presence of insoluble and soluble phosphate by P. putida P13 were 8.25 and 4.87 mg/g, respectively. Discussion and conclusion: Application of insoluble phosphate could increase K release from mica minerals. The enhanced releasing of mineral K might be attributed to the release of organic acids from the bacteria, a mechanism which plays a pivotal role in solubilizing phosphate from inorganic source of phosphate.

  17. Origin and nature of the aluminium phosphate-sulfate minerals (APS) associated with uranium mineralization in triassic red-beds (Iberian Range, Spain)

    Energy Technology Data Exchange (ETDEWEB)

    Marfil, R.; Iglesia, A. la; Estupinan, J.

    2013-10-01

    This study focuses on the mineralogical and chemical study of an Aluminium-phosphate-sulphate (APS) mineralization that occurs in a classic sequence from the Triassic (Buntsandstein) of the Iberian Range. The deposit is constituted by sandstones, mud stones, and conglomerates with arenaceous matrix, which were deposited in fluvial to shallow-marine environments. In addition to APS minerals, the following diagenetic minerals are present in the classic sequence: quartz, K-feldspar, kaolinite group minerals, illite, Fe-oxides-hydroxides, carbonate-sulphate cement-replacements and secondary uraniferous minerals. APS minerals were identified and characterized by optical microscopy, X-ray diffraction, scanning electron microscopy, and electron microprobe. Microcrystalline APS crystals occur replacing uraniferous minerals, associated with kaolinite, mica and filling pores, in distal fluvial-to-tidal arkoses-subarkoses. Given their Ca, Sr, and Ba contents, the APS minerals can be defined as a solid solution of crandallite- goyacite-gorceixite (0.53 Ca, 0.46 Sr and 0.01 Ba). The chemical composition, low LREE concentration and Sr > S suggest that the APS mineral were originated during the supergene alteration of the Buntsandstein sandstones due to the presence of the mineralizing fluids which causes the development of Ubearing sandstones in a distal alteration area precipitating from partially dissolved and altered detrital minerals. Besides, the occurrence of dickite associated with APS minerals indicates they were precipitated at diagenetic temperatures (higher than 80 degree centigrade), related to the uplifting occurred during the late Cretaceous post-rift thermal stage.(Author)

  18. Electrolytic coating of calcium phosphate on titanium: optimisation of the conversion of monetite of hydroxyapatite

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, J.F.; Sena, L.A.; Soares, G.A. [Universitade Federal, Rio de Janeiro (Brazil). Materials Dept.; Prado da Silva, M.H. [Military Inst. of Engineering, Rio de Janeiro, RJ (Brazil); Rossi, A.M. [Brazilian Centre of Physical Research (CBPF), Rio de Janeiro, RJ (Brazil)

    2001-07-01

    Electrolytic deposition has been proposed as an alternative method of coating hydroxyapatite on metallic substrates. The aim of this study was to characterise the conversion process in order to determine the minimum time to complete the monetite to hydroxyapatite transformation. Titanium substrate coated with monetite by electrolytic deposition was treated with NaOH solution in different time points. XRD spectra indicated that a reaction time of four hours was enough to convert all monetite to hydroxyapatite. Carbonate in B and A sites of hydroxyapatite were identified by IR using the diffuse reflectance mode (DR-IR). However, DRX-IR analysis of the converted sample indicated that the resulting coating consists of hydroxyapatite with low carbonate content. (orig.)

  19. Mineral phosphate solubilization by Streptomyces sp. CTM396 involves the excretion of gluconic acid and is stimulated by humic acids.

    Science.gov (United States)

    Farhat, Mounira Ben; Boukhris, Ines; Chouayekh, Hichem

    2015-03-01

    The actinomycetes isolates (128) which were taken from agricultural soil samples and collected near a rock phosphate processing unit were screened for mineral phosphate-solubilizing (MPS) ability. A significant MPS activity was observed for 30 isolates on various phosphate sources when grown in the National Botanical Research Institute's phosphate broth. CTM396 and CTM397 strains which showed the highest MPS abilities were identified by 16S rDNA sequencing as members of the genus Streptomyces. Their MPS activity was proved to be concomitant with a drop in pH due to the secretion of gluconic acid (GA). This was correlated with the simultaneous detection by PCR of genes gdh [encoding the glucose dehydrogenase (GDH) responsible for GA production from glucose] and pqq (involved in biosynthesis of the pyrroloquinoline quinone cofactor of GDH), as well as the highlighting of GHD enzyme activity, for the first time in a Streptomyces sp. strain producing GA. Furthermore, the 0.05% of humic acids proved to have a stimulatory effect on the growth and the ability of CTM396 to solubilize Gafsa rock phosphate. According to this study, it is possible to use humic acids and Gafsa rock phosphate in association with spores of ad hoc Streptomyces strains as natural and efficient amendments to improve plant growth with no need of costly and pollutant transformation of Gafsa rock phosphate.

  20. High-performance scaffolds on titanium surfaces: Osteoblast differentiation and mineralization promoted by a globular fibrinogen layer through cell-autonomous BMP signaling

    Energy Technology Data Exchange (ETDEWEB)

    Horasawa, Noriko, E-mail: horasawa@po.mdu.ac.jp [Department of Dental Materials, Matsumoto Dental University, 1780 Hiro-oka Gobara, Shiojiri, Nagano 399-0781 (Japan); Yamashita, Teruhito [Institute for Oral Science, Matsumoto Dental University, 1780 Hiro-oka Gobara, Shiojiri, Nagano 399-0781 (Japan); Uehara, Shunsuke; Udagawa, Nobuyuki [Department of Biochemistry, Matsumoto Dental University, 1780 Hiro-oka Gobara, Shiojiri, Nagano 399-0781 (Japan)

    2015-01-01

    Titanium has been widely used as a dental implant material. However, it takes several months for the implant body to bind with the jawbone. To develop new bioactive modification on titanium surfaces to achieve full osseointegration expeditiously, we used fibrinogen and fibronectin as bioactive scaffolds on the titanium plate, which are common extracellular matrix (ECM) proteins. We analyzed the features of the surface of ECM-modified titanium plates by atomic force microscopy and Fourier transform infrared spectrophotometry. We also evaluated the effect of ECM modification on promoting the differentiation and mineralization of osteoblasts on these surfaces. Fibrinogen had excellent adsorption on titanium surfaces even at low concentrations, due to the binding ability of fibrinogen via its RGD motif. The surface was composed of a fibrinogen monolayer, in which the ratio of β-sheets was decreased. Osteoblast proliferation on ECM-modified titanium surface was significantly promoted compared with titanium alone. Calcification on the modified surface was also accelerated. These ECM-promoting effects correlated with increased expression of bone morphogenetic proteins (BMPs) by the osteoblasts themselves and were inhibited by Noggin, a BMP inhibitor. These results suggest that the fibrinogen monolayer-modified titanium surface is recognized as bioactive scaffolds and promotes bone formation, resulting in the acceleration of osseointegration. - Highlights: • Fibrinogen had an excellent adsorption on titanium at low concentrations. • Fibrinogen on titanium formed composite layer with a decrease in β-sheet structure. • Osteoblast proliferation and calcification on the ECM-modified titanium plates were significant. • These effects of fibrinogen were increased of BMPs by osteoblasts themselves. • The scaffolds of fibrinogen on titanium might accelerate osseointegration.

  1. Modulation of small intestinal phosphate transporter by dietary supplements of mineral phosphorus and phytase in broilers.

    Science.gov (United States)

    Huber, Korinna; Zeller, Ellen; Rodehutscord, Markus

    2015-05-01

    Dietary phosphorus (P) is known as a main modulator of phosphate (Pi) transporter expression. The effect of supplemented mineral P with or without phytase on protein expression of two sodium-dependent Pi (NaPi) transporters and a calcium channel was studied in the small intestine of broilers. Thirty-six broilers were randomly assigned to six different diets at 15 days of age. Two levels of total P (tP, adjusted by monocalcium phosphate (MCP) supplementation), 0.39% (BD-) and 0.47% (BD+) were fed until day 25; and at each tP level, three levels of phytase were used with 0, 500, and 12,500 FTU/kg of an E. coli phytase. Mucosa samples from jejunum and ileum were taken and apical membranes were isolated by MgCl2 precipitation. Protein expression of NaPi IIb, NaPi type III (PiT1) and the calcium channel TRPV6 were semiquantitatively measured by Western blotting and jejunal mucosal phytase activity by measurement of Pi release. The jejunal NaPi IIb transporter was expressed with two distinct bands, which were modulated differently by diet. NaPi IIb Band1 increased (P phytase supplementation but was not affected by MCP supplementation. This inverse modulation of Band1 and Band2 was significantly related to the amount of net absorbed P with higher expression of Band1 at higher amounts of net absorbed P. In addition, a second Pi transporter, PiT1, was detected in which ileal expression decreased (P phytase supplementation. The expression of the calcium channel TRPV6 was increased in BD+ groups. A trend for an interaction between MCP and phytase supplementation on mucosal phytase activity was observed (P = 0.079) with a decrease in activity when BD+ with 12,500 FTU/kg phytase was fed. Chicken intestinal epithelial cells responded to dietary supplemented phytase and MCP by changing the Pi transporter expression in apical membranes. In conclusion, availability of Pi is most likely the key modulator of transporter protein expression. However, a contribution of lower inositol

  2. Zirconium-titanium-phosphate nanoparticles. Triton X-100 based size modification, characterization and application in radiochemical separation

    Energy Technology Data Exchange (ETDEWEB)

    Chakraborty, R.; Sen, B.; Chattopadhyay, P. [Burdwan Univ. (India). Dept. of Chemistry

    2014-07-01

    Zirconium-titanium-phosphate nanoparticles (ZTP) of different sizes were synthesized using tritron X-100 (polyethylene glycol-p-isooctylphenyl ether) surfactant. The materials were characterized by FTIR and powdered X-ray diffraction (XRD). The structural and morphological details of the material were obtained by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The SEM study was followed by energy dispersive spectroscopic analysis (EDS) for elemental analysis of the sample. The important peaks of the XRD spectra were analyzed to determine the probable composition of the material. The particle sizes were determined by dynamic light scattering (DLS) method. Ion exchange capacity was measured for different metal ions with sizes of the ZTP nanoparticles and size-dependent ion exchange property of the material was investigated thoroughly. The nanomaterial of the smallest size of around 5 nm was employed to separate carrier-free {sup 137m}Ba from {sup 137}Cs in column chromatographic technique using 1.0 M HNO{sub 3} as eluting agent at pH = 5. (orig.)

  3. Formation and properties of micro-arc wollastonite-calcium phosphate coatings on titanium and zirconium-niobium alloy

    Science.gov (United States)

    Sedelnikova, M. B.; Komarova, E. G.; Sharkeev, Yu. P.; Shinzhina, A. A.

    2016-11-01

    Wollastonite-calcium phosphate (W-CaP) coatings were deposited by the micro-arc oxidation (MAO) method on titanium (Ti) and Zr-1 wt % Nb (Zr-1Nb) alloy. The voltage of 150-300 V generated the MAO process with initial current amplitudes of 150-550 A and 100-350 A for Ti and Zr-1Nb substrates, respectively. Thin W-CaP coatings with the thickness of 10-11 µm were formed on Ti and Zr-1Nb under the low process voltage of 130-150 V. Elongated wollastonite particles with the size in the range of 40-100 µm were observed in such coatings. The structure of the coatings on Ti was mainly in X-ray amorphous state. In this case, X-ray reflexes relating to the crystalline phases of Ti and wollastonite were observed only in XRD patterns of the coatings deposited under 150-200 V. While, the crystalline structure with phases of CaZr4(PO4)6, β-ZrP2O7, ZrO2, and Zr was detected in the coatings on Zr-1Nb. FT-IRS, XRD, and SEM data confirmed that the increase of the process voltage up to 300 V leads to the dissociation of the wollastonite.

  4. Thin films of calcium phosphate and titanium dioxide by a sol-gel route: a new method for coating medical implants.

    Science.gov (United States)

    Piveteau, L D; Girona, M I; Schlapbach, L; Barboux, P; Boilot, J P; Gasser, B

    1999-03-01

    Titanium is a commonly used biomaterial for dental and orthopaedic applications. To increase its ability to bond with bone, some attempts were made to coat its surface with calcium phosphate (CaP). This paper describes a new type of coating. Instead of a pure CaP layer, a mixing of titanium dioxide (TIO2) and CaP is fabricated and deposited as a coating. These layers are deposited by a sol-gel route on pure titanium substrates using various pre-treatments. The method consists of mixing a solution of tetrabutyl ortho-titanate or a sol of titanium dioxide with a solution of calcium nitrate and phosphorous esters. This composite is deposited on to commercially pure titanium plates, mechanically polished or blasted with pure crystalline aluminum oxide, using the spin-coating technique. These coatings are then fired at 650 or 850 degrees C for various times. The samples are characterized by X-ray diffraction for their crystallinity, X-ray photoelectron spectroscopy for their surface chemical composition and scanning electron microscopy for their topography. Samples treated at 850 degrees C present a well-pronounced crystallinity, and a high chemical purity at the surface. The topography is strongly related to the viscosity of the precursor and the substrate pre-treatment. Possibilities to structure the outermost layer are presented.

  5. Estimating the thermodynamic properties of phosphate minerals at high and low temperature from the sum of constituent units

    Energy Technology Data Exchange (ETDEWEB)

    La Iglesia, A.

    2009-07-01

    Using the polyhedral units model of Hazen and employing a method of least-squares, the contribution of nineteen constituent units to the free energy and fifteen units to the enthalpy, at 298 K and 1 bar of pressure, have been calculated for mineral phosphates. The contribution of these constituent units to the free energy at higher temperatures has also been calculated. From these data we can estimate the thermodynamic properties of phosphates by summing the contribution of the distinct units, with more accuracy than the methods published up until now. (Author) 36 refs.

  6. Precipitation of Phosphate Minerals by Microorganisms Isolated from a Fixed-Biofilm Reactor Used for the Treatment of Domestic Wastewater

    Directory of Open Access Journals (Sweden)

    Almudena Rivadeneyra

    2014-04-01

    Full Text Available The ability of bacteria isolated from a fixed-film bioreactor to precipitate phosphate crystals for the treatment of domestic wastewater in both artificial and natural media was studied. When this was demonstrated in artificial solid media for crystal formation, precipitation took place rapidly, and crystal formation began 3 days after inoculation. The percentage of phosphate-forming bacteria was slightly higher than 75%. Twelve major colonies with phosphate precipitation capacity were the dominant heterotrophic platable bacteria growing aerobically in artificial media. According to their taxonomic affiliations (based on partial sequencing of the 16S rRNA, the 12 strains belonged to the following genera of Gram-negative bacteria: Rhodobacter, Pseudoxanthobacter, Escherichia, Alcaligenes, Roseobacter, Ochrobactrum, Agromyce, Sphingomonas and Paracoccus. The phylogenetic tree shows that most of the identified populations were evolutionarily related to the Alphaproteobacteria (91.66% of sequences. The minerals formed were studied by X-ray diffraction, scanning electron microscopy (SEM, and energy dispersive X-ray microanalysis (EDX. All of these strains formed phosphate crystals and precipitated struvite (MgNH4PO4·6H2O, bobierrite [Mg3(PO42·8H2O] and baricite [(MgFe3(PO42·8H2O]. The results obtained in this study show that struvite and spherulite crystals did not show any cell marks. Moreover, phosphate precipitation was observed in the bacterial mass but also near the colonies. Our results suggest that the microbial population contributed to phosphate precipitation by changing the media as a consequence of their metabolic activity. Moreover, the results of this research suggest that bacteria play an active role in the mineral precipitation of soluble phosphate from urban wastewater in submerged fixed-film bioreactors.

  7. Characterization of the aspects of osteoprogenitor cell interactions with physical tetracalcium phosphate anchorage on titanium implant surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Ko, Chia-Ling [Advanced Medical Devices and Composites Laboratory, Department of Fiber and Composite Materials, Feng Chia University, Taichung 40724, Taiwan (China); Dental Medical Devices and Materials Research Center, College of Dental Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan (China); Chang, Ya-Yuan; Liou, Cian-Hua [Alliance Global Technology Co., Ltd., Kaohsiung Medical Device Special Zone in Southern Taiwan Science Park, Kaohsiung 82151, Taiwan (China); Chen, Wen-Cheng, E-mail: wencchen@fcu.edu.tw [Advanced Medical Devices and Composites Laboratory, Department of Fiber and Composite Materials, Feng Chia University, Taichung 40724, Taiwan (China)

    2015-04-01

    Well-designed implants are used not only to modify the geometry of the implant but also to change the chemical properties of its surfaces. The present study aims to assess the biofunctional effects of tetracalcium phosphate (TTCP) particles as a physical anchor on the implant surface derived through sandblasting. The characteristics of the surface, cell viability, and alkaline phosphatase (ALP) activity toward osteoprogenitor cells (D1) were obtained. D1 cells were cultured on a plain surface that underwent sandblasting and acid etching (SLA) (control SLA group) and on different SLA surfaces with different anchoring TTCP rates (new test groups, M and H). The mean anchoring rates were 57% (M) and 74% (H), and the anchored thickness was estimated to range from 12.6 μm to 18.3 μm. Compared with the control SLA surface on Ti substrate, the new test groups with different TTCP anchoring rates (M and H) failed to improve cell proliferation significantly but had a well-differentiated D1 cell phenotype that enhanced ALP expression in the early stage of cell cultures, specifically, at day 7. Results suggest that the SLA surface with anchored TTCP can accelerate progenitor bone cell mineralization. This study shows the potential clinical application of the constructed geometry in TTCP anchorage on Ti for dental implant surface modification. - Highlights: • TTCP (tetracalcium phosphate) as a physical anchorage on implant is characterized. • Theoretical values of anchored thickness and capping areas were estimated. • TTCP anchored by sandblasting can accelerate progenitor bone cell mineralization. • TTCP anchored on SLA (sandblasting and acid etching) surface is a promising method.

  8. High-performance scaffolds on titanium surfaces: osteoblast differentiation and mineralization promoted by a globular fibrinogen layer through cell-autonomous BMP signaling.

    Science.gov (United States)

    Horasawa, Noriko; Yamashita, Teruhito; Uehara, Shunsuke; Udagawa, Nobuyuki

    2015-01-01

    Titanium has been widely used as a dental implant material. However, it takes several months for the implant body to bind with the jawbone. To develop new bioactive modification on titanium surfaces to achieve full osseointegration expeditiously, we used fibrinogen and fibronectin as bioactive scaffolds on the titanium plate, which are common extracellular matrix (ECM) proteins. We analyzed the features of the surface of ECM-modified titanium plates by atomic force microscopy and Fourier transform infrared spectrophotometry. We also evaluated the effect of ECM modification on promoting the differentiation and mineralization of osteoblasts on these surfaces. Fibrinogen had excellent adsorption on titanium surfaces even at low concentrations, due to the binding ability of fibrinogen via its RGD motif. The surface was composed of a fibrinogen monolayer, in which the ratio of β-sheets was decreased. Osteoblast proliferation on ECM-modified titanium surface was significantly promoted compared with titanium alone. Calcification on the modified surface was also accelerated. These ECM-promoting effects correlated with increased expression of bone morphogenetic proteins (BMPs) by the osteoblasts themselves and were inhibited by Noggin, a BMP inhibitor. These results suggest that the fibrinogen monolayer-modified titanium surface is recognized as bioactive scaffolds and promotes bone formation, resulting in the acceleration of osseointegration.

  9. Characterization of mineral phosphate solubilization traits from a barley rhizosphere soil functional metagenome.

    Science.gov (United States)

    Chhabra, Sagar; Brazil, Dina; Morrissey, John; Burke, James I; O'Gara, Fergal; N Dowling, David

    2013-10-01

    Mineral phosphate solubilization (MPS) microorganisms are important for their provision of orthophosphate anions for plant growth promotion activity in soil. In this study, we applied a functional metagenomic approach to identify this trait directly from the microbiome in barley rhizosphere soil that had not received P fertilizer over a 15-year period. A fosmid system was used to clone the metagenome of which 18,000 clones (~666 Mb of DNA) was screened for MPS. Functional assays and High Performance Liquid Chromatography analysis recognized gluconic acid production and MPS activity in the range 24.8-77.1 mmol/L and 27.6-38.16 μg/mL, respectively, when screened in an Escherichia coli host (at frequency of one MPS-positive clone hit per 114 Mb DNA tested). The MPS clones (with average insert size of ~37 kb) were analysed by 454 Roche sequencing and annotated. A number of genes/operons with homology to Phosphorous (P) uptake, regulatory and solubilization mechanisms were identified, linking the MPS function to the uncultivated microbiome present in barley rhizosphere soil.

  10. Hydroxyapatite/b-tricalcium Phosphate Composite for Guiding Bone Tissue Growth into a Titanium Tube in 8 mm Dog Tibia Cavity Defects

    Institute of Scientific and Technical Information of China (English)

    ZHU Jixiang; CHEN Xiaoming; WANG Jing; CHEN Weimin

    2016-01-01

    We developed a ifxation method and evaluate bone regrowth in the cavities of af4 mm× 8 mm titanium (Ti) tube through porous hydroxyapatite (HAP)/β-tricalcium phosphate (β-TCP) composite filling (group A), chitosan/calcium phosphate composite filling (group B), and HAP particle modification (group C). After 2 and 5 months of implantation in dog tibia defects, new bone formation in the three groups was studied by histology and histomorphometry. Group A displayed the most bone regenerated area in both 2 and 5 months post-operation. The chitosan/calcium phosphate composite in group B mostly degraded 2 months after implantation, leading to ifbrous tissue invasion after 5 months. By contrast, less bone formation was observed in group C. These results indicated that filling the cavities of metal prostheses with a porous HAP/β-TCP composite can be used for stable long-term ifxation in clinical settings.

  11. Environmental benefits of using magnesium carbonate minerals as new wildfire retardants instead of commercially available, phosphate-based compounds.

    Science.gov (United States)

    Liodakis, S; Tsoukala, M

    2010-10-01

    A serial batch leaching experiment has been carried out to evaluate the release of elements from the ash of Pinus halepensis needles burned under two test conditions-with and without treatment of the forest species with the carbonate minerals (huntite and hydromagnesite) in aqueous solution (pH 6). The ash (before and after leaching) and leachates were analyzed using atomic absorption spectroscopy and X-ray diffraction. Compared with data from samples treated with the commercially available, phosphate-based fire retardant diammonium phosphate (DAP), we found that use of huntite or hydromagnesite was much more successful in obstructing the release of the toxic elements present in the ash, probably because of the alkaline conditions resulting from decomposition of the minerals during burning. In contrast, DAP tended to be more able to facilitate the extraction of some toxic metals (e.g., Zn, Cu, Mn), probably because of the acidic conditions resulting from its decomposition to phosphoric acid. Data from this study thus lend strong support to the use of magnesium carbonate minerals as new wildfire retardants, because they were shown to be more friendly to the environment (e.g., soil, ground, and underground water streams) than those currently in use (e.g., phosphate or sulfate salt type).

  12. Geochemistry of phosphatic-shales and associated authigenic minerals of the Miocene Monterey Formation: Implications for paragenetic evolution

    Science.gov (United States)

    Sandoval, A.; Loyd, S. J.

    2016-12-01

    The Monterey Formation is a petroleum source and reservoir rock in California that was deposited in several basins during the tectonically-active Middle Miocene. The middle carbonaceous marl member of the Monterey Formation contains intervals of phosphatic-shales that are rhythmically cemented by dolomite as layers and concretions. Diagenetic minerals can form as the result of organic matter remineralization facilitated by microbes utilizing oxygen, nitrate, iron (III), sulfate and fermentation products as electron acceptors. Precipitation of phosphate and carbonate minerals tends to occur in suboxic-anoxic sediments, generally experiencing sulfate reduction, where degradation of organic matter yields alkalinity, sulfide and phosphate ions. Here, we present sulfur and carbon geochemical data in order to better characterize the conditions that led to the precipitation of phosphorous-rich minerals (e.g., carbonate-fluorapatite (CFA)) and dolomite that occur in close stratigraphic proximity. These data include concentration of CFA-associated sulfate, carbonate associated sulfate (CAS) and the respective δ°S values. The concentration of inorganic/organic carbon and associated δC values have been determined for CFA, dolomite and the host-shale, in order to further characterize the diagenetic environment of precipitation. These data indicate that authigenesis occurred in pore waters influenced by multiple microbial reactions, including respiration and methanogenesis reactions, and ultimately highlight the complexity of the Monterey diagenetic environment.

  13. Perfusion electrodeposition of calcium phosphate on additive manufactured titanium scaffolds for bone engineering.

    Science.gov (United States)

    Chai, Yoke Chin; Truscello, Silvia; Bael, Simon Van; Luyten, Frank P; Vleugels, Jozef; Schrooten, Jan

    2011-05-01

    A perfusion electrodeposition (P-ELD) system was reported to functionalize additive manufactured Ti6Al4V scaffolds with a calcium phosphate (CaP) coating in a controlled and reproducible manner. The effects and interactions of four main process parameters - current density (I), deposition time (t), flow rate (f) and process temperature (T) - on the properties of the CaP coating were investigated. The results showed a direct relation between the parameters and the deposited CaP mass, with a significant effect for t (P=0.001) and t-f interaction (P=0.019). Computational fluid dynamic analysis showed a relatively low electrolyte velocity within the struts and a high velocity in the open areas within the P-ELD chamber, which were not influenced by a change in f. This is beneficial for promoting a controlled CaP deposition and hydrogen gas removal. Optimization studies showed that a minimum t of 6 h was needed to obtain complete coating of the scaffold regardless of I, and the thickness was increased by increasing I and t. Energy-dispersive X-ray and X-ray diffraction analysis confirmed the deposition of highly crystalline synthetic carbonated hydroxyapatite under all conditions (Ca/P ratio=1.41). High cell viability and cell-material interactions were demonstrated by in vitro culture of human periosteum derived cells on coated scaffolds. This study showed that P-ELD provides a technological tool to functionalize complex scaffold structures with a biocompatible CaP layer that has controlled and reproducible physicochemical properties suitable for bone engineering.

  14. Photoactive layer-by-layer films of cellulose phosphate and titanium dioxide containing phosphotungstic acid

    Science.gov (United States)

    Ullah, Sajjad; Acuña, José Javier Sáez; Pasa, André Avelino; Bilmes, Sara A.; Vela, Maria Elena; Benitez, Guillermo; Rodrigues-Filho, Ubirajara Pereira

    2013-07-01

    A versatile layer-by-layer (LbL) procedure for the preparation of highly dispersed, adherent and porous multilayer films of TiO2 nanoparticles (NPs) and phosphotungstic acid (HPW) on a variety of substrates at room temperature was developed based on the use of cellulose phosphate (CP) as an efficient and non-conventional polyelectrolyte. UV/vis absorption spectroscopy confirmed the linear and regular growth of the films with the number of immersion cycles and a strong adsorption ability of CP towards TiO2 NPs. FTIR spectroscopy showed that HPW binds to the surface of TiO2 through the oxygen atom at the corner of the Keggin structure. XPS results showed that the interaction between TiO2 and CP is through Ti-O-P linkage. A model is proposed for the TiO2-HPW interaction based on XPS and FTIR results. FEG/SEM study of the surface morphology revealed a porous film structure with a homogenous distribution of the TiO2 NPs induced by CP. HRTEM studies showed that the resulting composite films consist of crystalline anatase and rutile phases and poly-nano-crystalline HPW with a semi-crystalline TiO2-HPW interface. These CP/TiO2 and CP/TiO2/HPW LbL films showed good photoactivity against both saturated and unsaturated species, for instance, stearic acid (SA), crystal violet (CV) and methylene blue (MB) under UV irradiation. The CP/HPW films formed on bacterial cellulose (BC) showed good photochromic response which is enhanced in presence of TiO2 due to an interfacial electron transfer from TiO2 to HPW. This simple and environmentally safe method can be used to form coatings on a variety of surfaces with photoactive TiO2 and TiO2/HPW films.

  15. Photoactive layer-by-layer films of cellulose phosphate and titanium dioxide containing phosphotungstic acid

    Energy Technology Data Exchange (ETDEWEB)

    Ullah, Sajjad [Instituto de Química de São Carlos, Universidade de São Paulo, PO Box 780, São Carlos, São Paulo 13564-970 (Brazil); Acuña, José Javier Sáez [Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo Andre, Sao Paulo, 09210-170 (Brazil); Pasa, André Avelino [Surface and Thin Film Laboratory, Physics Department, Federal University of Santa Catarina, PO Box 476, Florianópolis, SC 88040-900 (Brazil); Bilmes, Sara A. [Universidad de Buenos Aires, Facultad Ciencias Exactas y Naturales, Instituto de Química Física de los Materiales, Medio Ambiente y Energía – INQUIMAE, Ciudad Universitaria, Pab. 2, Buenos Aires C1428EHA (Argentina); Vela, Maria Elena; Benitez, Guillermo [Laboratorio de Nanoscopías y Fisicoquímica de Superficies, Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), Universidad Nacional de La Plata – CONICET, diagonal 113 esquina 64. C.C.16.Suc.4, 1900 La Plata (Argentina); Rodrigues-Filho, Ubirajara Pereira, E-mail: uprf@iqsc.usp.br [Instituto de Química de São Carlos, Universidade de São Paulo, PO Box 780, São Carlos, São Paulo 13564-970 (Brazil)

    2013-07-15

    A versatile layer-by-layer (LbL) procedure for the preparation of highly dispersed, adherent and porous multilayer films of TiO{sub 2} nanoparticles (NPs) and phosphotungstic acid (HPW) on a variety of substrates at room temperature was developed based on the use of cellulose phosphate (CP) as an efficient and non-conventional polyelectrolyte. UV/vis absorption spectroscopy confirmed the linear and regular growth of the films with the number of immersion cycles and a strong adsorption ability of CP towards TiO{sub 2} NPs. FTIR spectroscopy showed that HPW binds to the surface of TiO{sub 2} through the oxygen atom at the corner of the Keggin structure. XPS results showed that the interaction between TiO{sub 2} and CP is through Ti–O–P linkage. A model is proposed for the TiO{sub 2}–HPW interaction based on XPS and FTIR results. FEG/SEM study of the surface morphology revealed a porous film structure with a homogenous distribution of the TiO{sub 2} NPs induced by CP. HRTEM studies showed that the resulting composite films consist of crystalline anatase and rutile phases and poly-nano-crystalline HPW with a semi-crystalline TiO{sub 2}–HPW interface. These CP/TiO{sub 2} and CP/TiO{sub 2}/HPW LbL films showed good photoactivity against both saturated and unsaturated species, for instance, stearic acid (SA), crystal violet (CV) and methylene blue (MB) under UV irradiation. The CP/HPW films formed on bacterial cellulose (BC) showed good photochromic response which is enhanced in presence of TiO{sub 2} due to an interfacial electron transfer from TiO{sub 2} to HPW. This simple and environmentally safe method can be used to form coatings on a variety of surfaces with photoactive TiO{sub 2} and TiO{sub 2}/HPW films.

  16. Biomimetic and electrolytic calcium phosphate coatings on titanium alloy: physicochemical characteristics and cell attachment.

    Science.gov (United States)

    Wang, J; Layrolle, P; Stigter, M; de Groot, K

    2004-02-01

    Biomimetically deposited octacalcium phosphate (OCP) and carbonate apatite (BCA) as well as electrolytically deposited carbonate apatite (ECA) were considered as promising alternatives to conventional plasma spraying hydroxyapatite. This study compared their physicochemical characteristics and cell attachment behavior. The physicochemical characteristics included scanning electron microscopy observation, X-ray diffraction analysis, Fourier transform infrared spectroscopy analysis, surface roughness, coating thickness, dissolution test and scratch test. Cell attachment tests included morphology observation with stereomicroscopy and scanning electron microscopy as well as cell number count with DNA content assay. The OCP coating had 100% crystallinity and was about 40 microm thick, composed of large plate-like crystals of 30 microm, with the lowest surface roughness (R(a)=2.33 microm). The BCA coating had 60% crystallinity and was approximately 30 microm in thickness, composed of small crystals of 1-2 microm in size, with the highest surface roughness (R(a)=4.83 microm). The ECA coating had intermediate characteristics, with 78% crystallinity, 45 microm thickness, crystals of 5-6 microm and an average roughness of 3.87 microm. All coatings could be seen by eyes dissolving quickly and completely into acidic simulated body fluid (simulated physiological solutions-SPS, pH 3.0) but slowly and incompletely into neutral SPS (pH 7.3). It was suggested that the main factor determining coating dissolution in acidic SPS was the solubility isotherm, while some other factors including crystallinity and crystal size joined to determine coating dissolution in neutral SPS. In regard to adhesive strength, results of scratch test showed the critical load at the first crack of coating (L(c1)) was tightly related to crystal size as well as their arrangement, while the critical load at the total delamination of coating (L(c2)) was also related to the coating thickness. The ECA coating

  17. Effects of sandblasting, H2SO4/HCl etching, and phosphate primer application on bond strength of veneering resin composite to commercially pure titanium grade 4.

    Science.gov (United States)

    Egoshi, Takafumi; Taira, Yohsuke; Soeno, Kohyoh; Sawase, Takashi

    2013-01-01

    This study investigated the effects of surface treatments on the bond strength of a resin composite to a commercially pure titanium. The bonding surfaces of all titanium specimens were ground with 1,000-grit silicon carbide paper and then subjected to one or more of these surface treatments: sandblasting with alumina (sand), etching with 45wt% H2SO4 and 15wt% HCl (SH-etchant) at 70°C for 10 min, and/or phosphate primer (MDP-primer) application. Specimens not subjected to any surface treatment were used as controls. After resin composite veneer placement and 24-h water immersion, the shear bond strengths of the specimens in descending order were: sand/SH-etchant/MDP-primer, sand/SH-etchant/no primer, no sand/SH-etchant/MDP-primer, sand/no etch/MDP-primer, no sand/SH-etchant/no primer, sand/no etch/no primer, no sand/no etch/MDP-primer, no sand/no etch/no primer. Scanning electron microscope observations revealed that sandblasting and SH-etchant created many micro- and nanoscale cavities on the titanium surface. Results showed that a combined use of sandblasting, SH-etchant, and MDP-primer application had a cooperative effect on titanium bonding.

  18. Effect of surface alkali-based treatment of titanium implants on ability to promote in vitro mineralization and in vivo bone formation.

    NARCIS (Netherlands)

    Camargo, W.A.; Takemoto, S.; Hoekstra, J.W.M.; Leeuwenburgh, S.C.G.; Jansen, J.A.; Beucken, J.J.J.P van den; Alghamdi, H.S.

    2017-01-01

    This study investigated whether a novel alkali-based surface modification enhances in vitro mineralization as well as in vivo bone formation around titanium (Ti) implants in a femoral condyle model of 36 male Wister rats. All implant surfaces were grit-blasted and then received either acid-etching t

  19. Kinetic and Thermodynamic Studies on the Phosphate Adsorption Removal by Dolomite Mineral

    OpenAIRE

    Xiaoli Yuan; Wentang Xia; Juan An; Jianguo Yin; Xuejiao Zhou; Wenqiang Yang

    2015-01-01

    The efficiency of dolomite to remove phosphate from aqueous solutions was investigated. The experimental results showed that the removal of phosphate by dolomite was rapid (the removal rate over 95% in 60 min) when the initial phosphate concentration is at the range of 10–50 mg/L. Several kinetic models including intraparticle diffusion model, pseudo-first-order model, Elovich model, and pseudo-second-order model were employed to evaluate the kinetics data of phosphate adsorption onto dolomit...

  20. Surface characterization and corrosion behavior of calcium phosphate-base composite layer on titanium and its alloys via plasma electrolytic oxidation: A review paper.

    Science.gov (United States)

    Rafieerad, A R; Ashra, M R; Mahmoodian, R; Bushroa, A R

    2015-12-01

    In recent years, calcium phosphate-base composites, such as hydroxyapatite (HA) and carbonate apatite (CA) have been considered desirable and biocompatible coating layers in clinical and biomedical applications such as implants because of the high resistance of the composites. This review focuses on the effects of voltage, time and electrolytes on a calcium phosphate-base composite layer in case of pure titanium and other biomedical grade titanium alloys via the plasma electrolytic oxidation (PEO) method. Remarkably, these parameters changed the structure, morphology, pH, thickness and crystallinity of the obtained coating for various engineering and biomedical applications. Hence, the structured layer caused improvement of the biocompatibility, corrosion resistance and assignment of extra benefits for Osseo integration. The fabricated layer with a thickness range of 10 to 20 μm was evaluated for physical, chemical, mechanical and tribological characteristics via XRD, FESEM, EDS, EIS and corrosion analysis respectively, to determine the effects of the applied parameters and various electrolytes on morphology and phase transition. Moreover, it was observed that during PEO, the concentration of calcium, phosphor and titanium shifts upward, which leads to an enhanced bioactivity by altering the thickness. The results confirm that the crystallinity, thickness and contents of composite layer can be changed by applying thermal treatments. The corrosion behavior was investigated via the potentiodynamic polarization test in a body-simulated environment. Here, the optimum corrosion resistance was obtained for the coating process condition at 500 V for 15 min in Ringer solution. This review has been summarized, aiming at the further development of PEO by producing more adequate titanium-base implants along with desired mechanical and biomedical features.

  1. Osteocyte regulation of phosphate homeostasis and bone mineralization underlies the pathophysiology of the heritable disorders of rickets and osteomalacia.

    Science.gov (United States)

    Feng, Jian Q; Clinkenbeard, Erica L; Yuan, Baozhi; White, Kenneth E; Drezner, Marc K

    2013-06-01

    Although recent studies have established that osteocytes function as secretory cells that regulate phosphate metabolism, the biomolecular mechanism(s) underlying these effects remain incompletely defined. However, investigations focusing on the pathogenesis of X-linked hypophosphatemia (XLH), autosomal dominant hypophosphatemic rickets (ADHR), and autosomal recessive hypophosphatemic rickets (ARHR), heritable disorders characterized by abnormal renal phosphate wasting and bone mineralization, have clearly implicated FGF23 as a central factor in osteocytes underlying renal phosphate wasting, documented new molecular pathways regulating FGF23 production, and revealed complementary abnormalities in osteocytes that regulate bone mineralization. The seminal observations leading to these discoveries were the following: 1) mutations in FGF23 cause ADHR by limiting cleavage of the bioactive intact molecule, at a subtilisin-like protein convertase (SPC) site, resulting in increased circulating FGF23 levels and hypophosphatemia; 2) mutations in DMP1 cause ARHR, not only by increasing serum FGF23, albeit by enhanced production and not limited cleavage, but also by limiting production of the active DMP1 component, the C-terminal fragment, resulting in dysregulated production of DKK1 and β-catenin, which contributes to impaired bone mineralization; and 3) mutations in PHEX cause XLH both by altering FGF23 proteolysis and production and causing dysregulated production of DKK1 and β-catenin, similar to abnormalities in ADHR and ARHR, but secondary to different central pathophysiological events. These discoveries indicate that ADHR, XLH, and ARHR represent three related heritable hypophosphatemic diseases that arise from mutations in, or dysregulation of, a single common gene product, FGF23 and, in ARHR and XLH, complimentary DMP1 and PHEX directed events that contribute to abnormal bone mineralization.

  2. Kinetic and Thermodynamic Studies on the Phosphate Adsorption Removal by Dolomite Mineral

    Directory of Open Access Journals (Sweden)

    Xiaoli Yuan

    2015-01-01

    Full Text Available The efficiency of dolomite to remove phosphate from aqueous solutions was investigated. The experimental results showed that the removal of phosphate by dolomite was rapid (the removal rate over 95% in 60 min when the initial phosphate concentration is at the range of 10–50 mg/L. Several kinetic models including intraparticle diffusion model, pseudo-first-order model, Elovich model, and pseudo-second-order model were employed to evaluate the kinetics data of phosphate adsorption onto dolomite and pseudo-second-order model was recommended to describe the adsorption kinetics characteristics. Further analysis of the adsorption kinetics indicated that the phosphate removal process was mainly controlled by chemical bonding or chemisorption. Moreover, both Freundlich and Langmuir adsorption isotherms were used to evaluate the experimental data. The results indicated that Langmuir isotherm was more suitable to describe the adsorption characteristics of dolomite. Maximum adsorption capacity of phosphate by dolomite was found to be 4.76 mg phosphorous/g dolomite. Thermodynamic studies showed that phosphate adsorption was exothermic. The study implies that dolomite is an excellent low cost material for phosphate removal in wastewater treatment process.

  3. Adsorption of Nucleic Acid Bases, Ribose, and Phosphate by Some Clay Minerals

    OpenAIRE

    Hideo Hashizume

    2015-01-01

    Besides having a large capacity for taking up organic molecules, clay minerals can catalyze a variety of organic reactions. Derived from rock weathering, clay minerals would have been abundant in the early Earth. As such, they might be expected to play a role in chemical evolution. The interactions of clay minerals with biopolymers, including RNA, have been the subject of many investigations. The behavior of RNA components at clay mineral surfaces needs to be assessed if we are to appreciate ...

  4. Discussion: The timing of gold mineralization across the eastern Yilgarn Craton using U-Pb geochronology of hydrothermal phosphate minerals

    Science.gov (United States)

    Bateman, Roger; Jones, Sarah

    2015-10-01

    The presentation of recent geochronological work on orogenic gold deposits in the Eastern Goldfields of the Yilgarn Craton, Western Australia, claims to prove that there is a single broad event of gold mineralization and that structural work demonstrating that there are a number of discrete gold mineralization events is wrong. This new data demonstrates no such thing, as this data, no doubt the best that can currently be produced, shows a very wide and inconsistent range in ages. Geochronology is not yet able to reliably separate these events, which appear to be spread over an interval of perhaps 30 Ma, up to ˜2635 Ma.

  5. Effects of Organic Anions on Phosphate Adsorption and Desorption from Variable—Charge Clay Minerals and Soil

    Institute of Scientific and Technical Information of China (English)

    HEZHEN-LI; YUANKE-NENG; 等

    1992-01-01

    Effects of citrate and tartrate on phosphate adsorption and desorption from kaolinite,goethite,amorphous Al-oxide and Ultisol were studied.P adsorption was significantly decreased as the concentration of the organic anions increased from 10-5 to 10-1 M.At 0.1 M and pH 7.0,tartrate decreased P adsorption by 27.6%-50.6% and citrate by 37.9-80.4%,depending on the kinds of adsorbent.Little Al and/or Fe were detected in the equilibrium solutions,even at the highest concentration of the organic anions.Effects of the organic anions on phosphate adsorption follow essentially the competitive adsorption mechanism.The selectivity coefficients for competitive adsorption can be used to compare the effectiveness of different organic anions in reducing P adsorption under given gonditions. Phosphate desorption was increased by 3 to 100 times in the presence of 0.001 M citrate or tartrate compared to that in 0.02 M KCl solution alone.However,for all the soil and clay minerals studied the amount of P desorbed by citrate or tartrate was generally lower than or close to that of isotopically exchangeable P.The effect of organic anions on phosphate desorption arises primarily from ligand exchange.

  6. Post-prandial changes in plasma mineral levels in rainbow trout fed a complete plant ingredient based diet and the effect of supplemental di-calcium phosphate

    NARCIS (Netherlands)

    Antony Jesu Prabhu, P.; Schrama, J.W.; Mariojouls, C.; Godin, S.; Fontagné-Dicharry, S.; Geurden, I.; Surget, A.; Bouyssiere, B.; Kaushik, S.J.

    2014-01-01

    Post-prandial changes in plasma mineral levels and utilisation of minerals in rainbow trout fed complete plant ingredient based diets with or without supplemental di-calcium phosphate (DCP) were studied over an 8 week period. Three diets were used: diet M was FM and fish oil (FO) based diet (control

  7. Development of value-added products from alumina industry mineral wastes using low-temperature-setting phosphate ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Wagh, A.S.; Jeong, Seung-Young; Singh, D.

    1996-01-01

    A room-temperature process for stabilizing mineral waste streams has been developed, based on acid-base reaction between MgO and H3PO4 or acid phosphate solution. The resulting waste form sets into a hard ceramic in a few hours. In this way, various alumina industry wastes, such as red mud and treated potliner waste, can be solidified into ceramics which can be used as structural materials in waste management and construction industry. Red mud ceramics made by this process were low-porosity materials ({approx}2 vol%) with a compression strength equal to portland cement concrete (4944 psi). Bonding mechanism appears to be result of reactions of boehmite, goethite, and bayerite with the acid solution, and also encapsulation of red mud particles in Mg phosphate matrix. Possible applications include liners for ponds and thickned tailings disposal, dikes for waste ponds, and grouts. Compatability problems arising at the interface of the liner and the waste are avoided.

  8. Adsorption of nucleic Acid bases, ribose, and phosphate by some clay minerals.

    Science.gov (United States)

    Hashizume, Hideo

    2015-01-01

    Besides having a large capacity for taking up organic molecules, clay minerals can catalyze a variety of organic reactions. Derived from rock weathering, clay minerals would have been abundant in the early Earth. As such, they might be expected to play a role in chemical evolution. The interactions of clay minerals with biopolymers, including RNA, have been the subject of many investigations. The behavior of RNA components at clay mineral surfaces needs to be assessed if we are to appreciate how clays might catalyze the formation of nucleosides, nucleotides and polynucleotides in the "RNA world". The adsorption of purines, pyrimidines and nucleosides from aqueous solution to clay minerals is affected by suspension pH. With montmorillonite, adsorption is also influenced by the nature of the exchangeable cations. Here, we review the interactions of some clay minerals with RNA components.

  9. Adsorption of Nucleic Acid Bases, Ribose, and Phosphate by Some Clay Minerals

    Directory of Open Access Journals (Sweden)

    Hideo Hashizume

    2015-02-01

    Full Text Available Besides having a large capacity for taking up organic molecules, clay minerals can catalyze a variety of organic reactions. Derived from rock weathering, clay minerals would have been abundant in the early Earth. As such, they might be expected to play a role in chemical evolution. The interactions of clay minerals with biopolymers, including RNA, have been the subject of many investigations. The behavior of RNA components at clay mineral surfaces needs to be assessed if we are to appreciate how clays might catalyze the formation of nucleosides, nucleotides and polynucleotides in the “RNA world”. The adsorption of purines, pyrimidines and nucleosides from aqueous solution to clay minerals is affected by suspension pH. With montmorillonite, adsorption is also influenced by the nature of the exchangeable cations. Here, we review the interactions of some clay minerals with RNA components.

  10. Solid-state phosphorus-31 nuclear magnetic resonance studies of synthetic solid phases of calcium phosphate: potential models of bone mineral.

    Science.gov (United States)

    Aue, W P; Roufosse, A H; Glimcher, M J; Griffin, R G

    1984-12-04

    Phosphorus-31 NMR spectra have been obtained from a variety of synthetic, solid calcium phosphate mineral phases by magic angle sample spinning. The samples include crystalline hydroxyapatite, two type B carbonatoapatites containing 3.2 and 14.5% CO3(2-), respectively, a hydroxyapatite in which approximately 12% of the phosphate groups are present as HPO4(2-), an amorphous calcium phosphate, monetite, brushite, and octacalcium phosphate. Spectra were observed by the standard Bloch decay and cross-polarization techniques, as well as by a dipolar suppression sequence, in order to distinguish between protonated and unprotonated phosphate moieties. The spectra of the synthetic calcium phosphates provide basic information that is essential for interpreting similar spectra obtained from bone and other calcified tissues.

  11. Phosphated minerals to be used as radioactive reference materials; Minerais fosfatados para serem utilizados como materiais de referencia radioativos

    Energy Technology Data Exchange (ETDEWEB)

    Braganca, M.J.C.S.; Tauhata, L. [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil). Lab. Nacional de Metrologia das Radiacoes Ionizantes (LNMRI); Clain, A.F. [Universidade Severino Sombra, Vassouras, RJ (Brazil); Moreira, I. [Pontificia Univ. Catolica do Rio de Janeiro (PUC/Rio), RJ (Brazil). Dept. de Quimica

    2003-07-01

    The production and the supplying of certified reference materials, or deliberated contaminated materials containing natural radionuclides for laboratories which analyses environmental samples are fundamentals for the correct measurements of their radioactive levels. This analysis quality represents a important step for the safeguards of the population health, and quality control of the imported and exported products, such as minerals, agricultural and raw materials. The phosphate rocks, containing significant concentrations of thorium, and used as raw material and fertilizers justified a study for better characterization and distinction to be used cas certified reference radioactive materials. Therefore, samples from the two carboanalytical-alkaline chimneys (Araxa and Catalao), and one from metasedimentar origin (Patos de Minas), distant 100 km from each other, were collected and chemical and cholecystographic characterized by optical emission, X-ray diffraction and fluorescence. The element concentrations were determined by neutron activation analysis, ICP-MS and ICP-AES. The results, after multivariate statistical analysis and study of correlations among elements, have shown geochemical similarities of the phosphates from Araxa and Catalao, and differences from Patos de Minas, despite of the geographic proximity. The concentration of thorium between 200 and 500 (mg/g) allows to use such minerals as reference materials.

  12. Regulatory inhibition of biological tissue mineralization by calcium phosphate through post-nucleation shielding by fetuin-A

    Science.gov (United States)

    Chang, Joshua C.; Miura, Robert M.

    2016-04-01

    In vertebrates, insufficient availability of calcium and inorganic phosphate ions in extracellular fluids leads to loss of bone density and neuronal hyper-excitability. To counteract this problem, calcium ions are usually present at high concentrations throughout bodily fluids—at concentrations exceeding the saturation point. This condition leads to the opposite situation where unwanted mineral sedimentation may occur. Remarkably, ectopic or out-of-place sedimentation into soft tissues is rare, in spite of the thermodynamic driving factors. This fortunate fact is due to the presence of auto-regulatory proteins that are found in abundance in bodily fluids. Yet, many important inflammatory disorders such as atherosclerosis and osteoarthritis are associated with this undesired calcification. Hence, it is important to gain an understanding of the regulatory process and the conditions under which it can go awry. In this manuscript, we extend mean-field continuum classical nucleation theory of the growth of clusters to encompass surface shielding. We use this formulation to study the regulation of sedimentation of calcium phosphate salts in biological tissues through the mechanism of post-nuclear shielding of nascent mineral particles by binding proteins. We develop a mathematical description of this phenomenon using a countable system of hyperbolic partial differential equations. A critical concentration of regulatory protein is identified as a function of the physical parameters that describe the system.

  13. Regulation of Soluble Phosphate on the Ability of Phytate Mineralization and β-Propeller Phytase Gene Expression of Pseudomonas fluorescens JZ-DZ1, a Phytate-Mineralizing Rhizobacterium.

    Science.gov (United States)

    Shen, Lan; Wu, Xiao-Qin; Zeng, Qing-Wei; Liu, Hong-Bin

    2016-12-01

    Phytate-mineralizing rhizobacteria (PMR) play an important role in providing phosphorus for the sustainable plant growth. It is important to investigate the ability of PMR to produce phytase under different phosphate levels for its application. The effects of different concentrations of soluble phosphate on the ability of phytate mineralization of Pseudomonas fluorescens JZ-DZ1, a phytate-mineralizing rhizobacterium, were investigated in both solid and liquid media. The results on solid media showed that halo zone width gradually reduced with concentrations of soluble phosphate increasing from 0.05 to 20 mM, indicating the reduction of the ability of phytate mineralization. The results were consistent with the quantitative detection of phytase activity from the overall trend. An 1866-bp β-propeller phytase (BPP) gene (phyPf) was cloned from the strain, and the deduced amino acid sequence of phyPf shared 98 % of identity with a known BPP from Pseudomonas sp. BS10-3 (AJF36073.1). The results of relative real-time quantitative PCR assay showed that the expression of phyPf was induced by a low concentration (0.1 mM) of soluble phosphate, suggesting that BPP secretion was regulated by gene phyPf. The BPP-harboring bacterium P. fluorescens JZ-DZ1 with low phosphate-inducible ability of phytate mineralization could be potentially applied to promote phosphorus uptake for plants in the future.

  14. Characterization and corrosion resistance of anodic electrodeposited titanium oxide/phosphate films on Ti-20Nb-10Zr-5Ta bioalloy

    Energy Technology Data Exchange (ETDEWEB)

    Popa, Monica; Vasilescu, Cora; Drob, Silviu I.; Osiceanu, Petre; Anastasescu, Mihai; Calderon-Moreno, Jose M., E-mail: josecalderonmoreno@yahoo.com [Institute of Physical Chemistry ' Ilie Murgulescu' of the Romanian Academy, Bucharest (Romania)

    2013-07-15

    In this work, the anodic galvanostatic electrodeposition of an oxidation film containing phosphates on Ti-20Nb-10Zr-5Ta alloy from orthophosphoric acid solution is presented. Its composition was determined by X-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR) and Raman micro-spectroscopy, and its topography by atomic force microscopy (AFM). The corrosion resistance of the coated alloy in simulated human fluid (by linear polarization method and monitoring of open circuit potentials, corresponding open circuit potential gradients) as well as the characterization of the coating (by Raman spectroscopy and depth profile X-ray photoelectron spectroscopy (XPS)) deposited in a period of 300 h soaking in simulated human body fluid were studied. The electrodeposited film was composed of amorphous titanium dioxide and contained phosphate groups. The corrosion resistance of the coated Ti-20Nb-10Zr-5Ta alloy in neutral and alkaline Ringer's solutions was higher than that of the bare alloy due to the protective properties of the electrodeposited film. The corrosion parameters improved over time as result of the thickening of the surface film by the deposition from the physiological solution. The deposited coating presented a variable composition in depth: at the deeper layer nucleated nanocrystalline hydroxyapatite and at the outer layer amorphous calcium phosphate. (author)

  15. Dynamics and diversity of phosphate mineralizing bacteria in the coral reefs of Gulf of Mannar

    Digital Repository Service at National Institute of Oceanography (India)

    Kannapiran, E.; Ravindran, J.

    of the Bacillus species varied with reference to different pH. The species Bacillus megaterium (573) showed highest phosphate solubilizing activity (0.906 mmol/l P) by producing 2-ketogluconic acid. The production of organic acids and phosphatase enzymes...

  16. Phosphate geochemistry, mineralization processes, and Thioploca distribution in shelf sediments off central Chile

    DEFF Research Database (Denmark)

    Holmkvist, Lars; Arning, Esther T.; Küster-Heins, Kathrin

    2010-01-01

    mineralization, and occurrence of dense communities of the filamentous sulfur bacteria, Thioploca spp., on the continental shelf off central Chile during the austral summer when high phytoplankton productivity and anoxic bottom water prevailed. Freshly deposited phytodetritus stimulated extremely high sulfate...

  17. Phosphate geochemistry, mineralization processes, and Thioploca distribution in shelf sediments off central Chile

    DEFF Research Database (Denmark)

    Holmkvist, Lars; Arning, Esther T.; Küster-Heins, Kathrin

    2010-01-01

    mineralization, and occurrence of dense communities of the filamentous sulfur bacteria, Thioploca spp., on the continental shelf off central Chile during the austral summer when high phytoplankton productivity and anoxic bottom water prevailed. Freshly deposited phytodetritus stimulated extremely high sulfate...

  18. Phosphate-Based Mineralization of Arsenic in Contaminated Soil: A Potential Remediation Method for Soil and Groundwater

    Science.gov (United States)

    Neupane, G.; Donahoe, R. J.

    2009-12-01

    Soil arsenic contamination resulting from the use of arsenical compounds is a widespread environmental problem. A phosphate-based remediation method which has the potential to immobilize arsenic in both oxidizing and reducing subsurface systems is under laboratory investigation. Although phosphate treatments have been reported to be effective in removal of arsenic from contaminated water, its use in contaminated soils has not been tested. This study aims to (1) determine the competitive adsorption/desorption of arsenate and phosphate at surfaces of ferric hydroxide coated sand in the absence or presence of calcium ions, and (2) develop a method of arsenic fixation which involves phosphoric acid flushing of arsenic from contaminated soil and precipitation of arsenic as apatite-like phases. Ferric hydroxide is a significant arsenic sequestering constituent in soil. Phosphate competes with arsenate for adsorption sites on the ferric hydroxide surface. Batch adsorption experiments conducted using ferric hydroxide coated sand have indicated similar pH-controlled adsorption mechanisms for both arsenate and phosphate. The data obtained from the adsorption experiments is being used to guide the development of a phosphate-based method for soil and groundwater arsenic remediation. Batch experiments were performed using 3g of contaminated soil in contact with 45 ml of treatment fluid (a dilute phosphoric acid and calcium hydroxide solution). Solution samples were collected at 24, 72, 144, 312, and 384 hours, with continuous agitation at 200 rpm. Solution concentrations of phosphorus and calcium generally decreased with time and were primarily controlled by pH. It has been experimentally demonstrated that solution arsenic concentrations can be lowered by maintaining high pH with adequate calcium supply. A batch experiment conducted at pH > 11, using 1 kg of soil in contact with 1 liter of 0.25% H3PO4, precipitated a white material giving an XRD signature indicative of brushite

  19. Inhibition of Rac and ROCK Signalling Influence Osteoblast Adhesion, Differentiation and Mineralization on Titanium Topographies

    Science.gov (United States)

    Prowse, Paul D. H.; Elliott, Christopher G.; Hutter, Jeff; Hamilton, Douglas W.

    2013-01-01

    Reducing the time required for initial integration of bone-contacting implants with host tissues would be of great clinical significance. Changes in osteoblast adhesion formation and reorganization of the F-actin cytoskeleton in response to altered topography are known to be upstream of osteoblast differentiation, and these processes are regulated by the Rho GTPases. Rac and RhoA (through Rho Kinase (ROCK)). Using pharmacological inhibitors, we tested how inhibition of Rac and ROCK influenced osteoblast adhesion, differentiation and mineralization on PT (Pre-treated) and SLA (sandblasted large grit, acid etched) topographies. Inhibition of ROCK, but not Rac, significantly reduced adhesion number and size on PT, with adhesion size consistent with focal complexes. After 1 day, ROCK, but not Rac inhibition increased osteocalcin mRNA levels on SLA and PT, with levels further increasing at 7 days post seeding. ROCK inhibition also significantly increased bone sialoprotein expression at 7 days, but not BMP-2 levels. Rac inhibition significantly reduced BMP-2 mRNA levels. ROCK inhibition increased nuclear translocation of Runx2 independent of surface roughness. Mineralization of osteoblast cultures was greater on SLA than on PT, but was increased by ROCK inhibition and attenuated by Rac inhibition on both topographies. In conclusion, inhibition of ROCK signalling significantly increases osteoblast differentiation and biomineralization in a topographic dependent manner, and its pharmacological inhibition could represent a new therapeutic to speed bone formation around implanted metals and in regenerative medicine applications. PMID:23505566

  20. Inhibition of Rac and ROCK signalling influence osteoblast adhesion, differentiation and mineralization on titanium topographies.

    Directory of Open Access Journals (Sweden)

    Paul D H Prowse

    Full Text Available Reducing the time required for initial integration of bone-contacting implants with host tissues would be of great clinical significance. Changes in osteoblast adhesion formation and reorganization of the F-actin cytoskeleton in response to altered topography are known to be upstream of osteoblast differentiation, and these processes are regulated by the Rho GTPases. Rac and RhoA (through Rho Kinase (ROCK. Using pharmacological inhibitors, we tested how inhibition of Rac and ROCK influenced osteoblast adhesion, differentiation and mineralization on PT (Pre-treated and SLA (sandblasted large grit, acid etched topographies. Inhibition of ROCK, but not Rac, significantly reduced adhesion number and size on PT, with adhesion size consistent with focal complexes. After 1 day, ROCK, but not Rac inhibition increased osteocalcin mRNA levels on SLA and PT, with levels further increasing at 7 days post seeding. ROCK inhibition also significantly increased bone sialoprotein expression at 7 days, but not BMP-2 levels. Rac inhibition significantly reduced BMP-2 mRNA levels. ROCK inhibition increased nuclear translocation of Runx2 independent of surface roughness. Mineralization of osteoblast cultures was greater on SLA than on PT, but was increased by ROCK inhibition and attenuated by Rac inhibition on both topographies. In conclusion, inhibition of ROCK signalling significantly increases osteoblast differentiation and biomineralization in a topographic dependent manner, and its pharmacological inhibition could represent a new therapeutic to speed bone formation around implanted metals and in regenerative medicine applications.

  1. Phosphate-Solubilizing and -Mineralizing Abilities of Bacteria Isolated from Soils

    Institute of Scientific and Technical Information of China (English)

    TAO Guang-Can; TIAN Shu-Jun; CAI Miao-Ying; XIE Guang-Hui

    2008-01-01

    Microorganisms capable of solubilizing and mineralizing phosphorus (P) pools in soils are considered vital in promoting P bioavailability. The study was conducted to screen and isolate inorganic P-solubilizing bacteria (IPSB) and organic P-mineralizing bacteria (OPMB) in soils taken from subtropical flooded and temperate non-flooded soils, and to compare inorganic P-solubilizing and organic P-solubilizing abilities between IPSB and OPMB. Ten OPMB strains were isolated and identified as Bacillus cereus and Bacillus megaterium, and five IPSB strains as B. megaterium, Burkholderia caryophylli,Pseudomonas ciehorii, and Pseudomonas syringae. P-solubilizing and -mineralizing abilities of the strains were measured using the methods taking cellular P into account. The IPSB strains exhibited inorganic P-sohibilizing abilities ranging between 25.4-41.7 μg P mL-1 and organic P-mineralizing abilities between 8.2-17.8 μg P mL-1. Each of the OPMB strains also exhibited both solubilizing and mineralizing abilities varying from 4.4 to 26.5 μg P mL-1 and from 13.8 to 62.8 μg P mL-1, respectively. For both IPSB and OPMB strains, most of the P mineralized from the organic P source was incorporated into the bacterial cells as cellular P. A significantly negative linear correlation (P < 0.05) was found between culture pH and P solubilized from inorganic P by OPMB strains. The results suggested that P solubilization and mineralization could coexist in the same bacterial strain.

  2. Evaluation of implant calcium-phosphate materials depending on their mineral content

    Directory of Open Access Journals (Sweden)

    I. A. Talashova

    2012-01-01

    Full Text Available Biocompatibility of original implant calcium-phosphate materials was evaluated in the experiment on animals. The methods of radiological electron-probe microanalysis (REMA and light and scan electron microscopy (SEM were used. Studied materials had the properties of biodegradation, osteoinduction and osteoconduction at different extent. The materials with the composite maximally close to the the bone tissue had the greatest grade of biocompatibility.

  3. A study on equilibrium and kinetics of ion exchange of alkaline earth metals using an inorganic cation exchanger - zirconium titanium phosphate

    Indian Academy of Sciences (India)

    Amin Jignasa; Thakkar Rakesh; Chudasama Uma

    2006-03-01

    An advanced inorganic cation exchange material of the class of tetravalent metal acid (TMA) salt, zirconium titanium phosphate (ZTP), has been synthesized by a modified sol-gel technique. ZTP has been characterized by elemental analysis (ICP-AES), thermal analysis (TGA), FTIR and X-ray diffraction studies. The Nernst-Planck equation has been used to study the forward and reverse ion exchange kinetics of Mg (II), Ca (II), Sr (II) and Ba (II) with H (I) at four different temperatures. The mechanism of exchange is particle diffusion, as confirmed by the linear (dimensionless time parameter) vs (time) plots. The exchange process is thus controlled by the diffusion within the exchanger particles for the systems studied herein. Further, various kinetic parameters like self-diffusion coefficient (0), energy of activation () and entropy of activation (*) have been evaluated under conditions favouring a particle diffusion-controlled mechanism.

  4. Cs salt of tungstophosphoric acid-promoted zirconium titanium phosphate solid acid catalyst: An active catalyst for the synthesis of bisphenols

    Indian Academy of Sciences (India)

    Niranjan Biswal; Dipti Prakasini Das; Kulamani Parida

    2014-03-01

    A series of novel CsTPA-ZTP ( = 30, 40, 50, 60 and 80 wt%) solid acid composite catalysts were synthesized by ion-exchange process using cesium nitrate, tungstophosphoric acid (TPA), zirconium titanium phosphate (ZTP) with varied surface areas, acidities and microstructures. Detailed characterizations of the composite catalysts were done by Powder X-ray Diffraction (PXRD), Fourier Transform Infrared (FTIR) Spectroscopy, N2 adsorption desorption, Scanning Electron Microscopy (SEM-EDS) analysis, X-ray Photoelectron Spectroscopy (XPS) and Temperature Programmed Desorption (TPD).We have studied the catalytic activities, kinetics and reusability of the catalysts. 60CsTPA-ZTP is found to be an effective and re-usable catalyst for the synthesis of bisphenol A (BPA) and bisphenol F (BPF) using acetonitrile as solvent.

  5. Characterization and Catalytic Activity of Titanium-containing Aluminum Phosphate Prepared by Sol-gel and Nonuniform Precipitation for O-Alkylation of Catechol with Ethanol

    Institute of Scientific and Technical Information of China (English)

    PAN Chun-liu; ZHANG Wen-xiang; LI Xue-mei; JIANG Da-zhen; WU Tong-hao

    2003-01-01

    Three titanium-containing aluminum phosphate catalysts with a general formula Al0.77Ti0.23PO4 were prepared by the sol-gel method at room temperature(APTS), and a nonuniform precipitation procedure at room temperature(APTR) and under reflux(APTF), respectively. The structural features and the surface properties of the three catalysts were determined by means of the physical adsorption of nitrogen at liquid N2 temperature, XRD, UV-Vis, NH3-TPD and IR of adsorbed pyridine. The vapor phase O-alkylation of catechol with ethanol over the prepared catalysts was studied. It was found that the activity and the selectivity of these catalysts are greatly dependent on the preparation method, and catalyst APTF shows the highest activity and selectivity. The characterization evidence indicates that the weak Brnsted acid sites were more effective for the reaction.

  6. Characterization of the mineral phosphate-solubilizing activity of Pantoea agglomerans MMB051 isolated from an iron-rich soil in southeastern Venezuela (Bolívar State).

    Science.gov (United States)

    Sulbarán, Miguel; Pérez, Elizabeth; Ball, María M; Bahsas, Alí; Yarzábal, Luis Andrés

    2009-04-01

    The mineral phosphate-solubilizing (MPS) activity of a Pantoea agglomerans strain, namely MMB051, isolated from an iron-rich, acidic soil near Ciudad Piar (Bolívar State, Venezuela), was characterized on a chemically defined medium (NBRIP). Various insoluble inorganic phosphates, including tri-calcium phosphate [Ca(3)(PO(4))(2)], iron phosphate (FePO(4)), aluminum phosphate (AlPO(4)), and Rock Phosphate (RP) were tested as sole sources of P for bacterial growth. Solubilization of Ca(3)(PO(4))(2) was very efficient and depended on acidification of the external milieu when MMB051 cells were grown in the presence of glucose. This was also the case when RP was used as the sole P source. On the other hand, the solubilization efficiency toward more insoluble mineral phosphates (FePO(4) and AlPO(4)) was shown to be very low. Even though gluconic acid (GA) was detected on culture supernatants of strain MMB051, a consequence of the direct oxidation pathway of glucose, inorganic-P solubilization seemed also to be related to other processes dependent on active cell growth. Among these, proton release by ammonium (NH(4)(+) ) fixation appeared to be of paramount importance to explain inorganic-P solubilization mediated by strain MMB051. On the contrary, the presence of nitrate (NO(3)(-) ) salts as the sole N source affected negatively the ability of MMB051 cells to solubilize inorganic P.

  7. Modeling phosphate transport and removal in a compact bed filled with a mineral-based sorbent for domestic wastewater treatment

    Science.gov (United States)

    Herrmann, Inga; Jourak, Amir; Gustafsson, Jon Petter; Hedström, Annelie; Lundström, T. Staffan; Viklander, Maria

    2013-11-01

    Phosphorus filter units containing mineral-based sorbents with a high phosphate (PO4) binding capacity have been shown to be appropriate for removing PO4 in the treatment of domestic wastewater in on-site facilities. However, a better understanding of their PO4 removal mechanisms, and reactions that could lead to the formation of PO4 compounds, is required to evaluate the potential utility of candidate sorbents. Models based on data obtained from laboratory-scale experiments with columns of selected materials can be valuable for acquiring such understanding. Thus, in this study the transport and removal of PO4 in experiments with a laboratory-scale column filled with a commercial silicate-based sorbent were modeled, using the hydro-geochemical transport code PHREEQC. The resulting models, that incorporated the dissolution of calcite, kinetic constrains for the dissolution of calcium oxide (CaO) and wollastonite (CaSiO3), and the precipitation of amorphous tricalcium phosphate, Ca3(PO4)2, successfully simulated the removal of PO4 observed in the experiments.

  8. In vivo implantation of porous titanium alloy implants coated with magnesium-doped octacalcium phosphate and hydroxyapatite thin films using pulsed laser depostion.

    Science.gov (United States)

    Mróz, Waldemar; Budner, Bogusław; Syroka, Renata; Niedzielski, Kryspin; Golański, Grzegorz; Slósarczyk, Anna; Schwarze, Dieter; Douglas, Timothy E L

    2015-01-01

    The use of porous titanium-based implant materials for bone contact has been gaining ground in recent years. Selective laser melting (SLM) is a rapid prototyping method by which porous implants with highly defined external dimensions and internal architecture can be produced. The coating of porous implants produced by SLM with ceramic layers based on calcium phosphate (CaP) remains relatively unexplored, as does the doping of such coatings with magnesium (Mg) to promote bone formation. In this study, Mg-doped coatings of the CaP types octacalcium phosphate and hydroxyapatite (HA) were deposited on such porous implants using the pulsed laser deposition method. The coated implants were subsequently implanted in a rabbit femoral defect model for 6 months. Uncoated implants served as a reference material. Bone-implant contact and bone volume in the region of interest were evaluated by histopathological techniques using a tri-chromatographic Masson-Goldner staining method and by microcomputed tomography (µCT) analysis of the volume of interest in the vicinity of implants. Histopathological analysis revealed that all implant types integrated directly with surrounding bone with ingrowth of newly formed bone into the pores of the implants. Biocompatibility of all implant types was demonstrated by the absence of inflammatory infiltration by mononuclear cells (lymphocytes), neutrophils, and eosinophils. No osteoclastic or foreign body reaction was observed in the vicinity of the implants. µCT analysis revealed a significant increase in bone volume for implants coated with Mg-doped HA compared to uncoated implants.

  9. Are iron-phosphate minerals a sink for phosphorus in anoxic Black Sea sediments?

    Science.gov (United States)

    Dijkstra, Nikki; Kraal, Peter; Kuypers, Marcel M M; Schnetger, Bernhard; Slomp, Caroline P

    2014-01-01

    Phosphorus (P) is a key nutrient for marine organisms. The only long-term removal pathway for P in the marine realm is burial in sediments. Iron (Fe) bound P accounts for a significant proportion of this burial at the global scale. In sediments underlying anoxic bottom waters, burial of Fe-bound P is generally assumed to be negligible because of reductive dissolution of Fe(III) (oxyhydr)oxides and release of the associated P. However, recent work suggests that Fe-bound P is an important burial phase in euxinic (i.e. anoxic and sulfidic) basin sediments in the Baltic Sea. In this study, we investigate the role of Fe-bound P as a potential sink for P in Black Sea sediments overlain by oxic and euxinic bottom waters. Sequential P extractions performed on sediments from six multicores along two shelf-to-basin transects provide evidence for the burial of Fe-bound P at all sites, including those in the euxinic deep basin. In the latter sediments, Fe-bound P accounts for more than 20% of the total sedimentary P pool. We suggest that this P is present in the form of reduced Fe-P minerals. We hypothesize that these minerals may be formed as inclusions in sulfur-disproportionating Deltaproteobacteria. Further research is required to elucidate the exact mineral form and formation mechanism of this P burial phase, as well as its role as a sink for P in sulfide-rich marine sediments.

  10. Mahlmoodite, FeZr(PO4).4H2O, a new iron zirconium phosphate mineral from Wilson Springs, Arkansas

    Science.gov (United States)

    Milton, C.; McGee, J.J.; Evans, H.T.

    1993-01-01

    Small (phosphate tetrahedrate, FeZr(PO4)2.4H2O. This new mineral, named mahlmoodite, occurs as spherules of radiating fibers usually perched on crystals of pyroxene in vugs. The optical and crystallographic properties of mahlmoodite are described. -after Authors

  11. Development, characterisation and biocompatibility testing of a cobalt-containing titanium phosphate-based glass for engineering of vascularized hard tissues

    Energy Technology Data Exchange (ETDEWEB)

    Lee, In-Ho [Department of Nanobiomedical Science and WCU Research Center of Nanobiomedical Science, Dankook University, Chungnam 330-714 (Korea, Republic of); Yu, Hye-sun [Department of Nanobiomedical Science and WCU Research Center of Nanobiomedical Science, Dankook University, Chungnam 330-714 (Korea, Republic of); Department of Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE (United Kingdom); Lakhkar, Nilay J. [Division of Biomaterials and Tissue Engineering, Eastman Dental Institute, University College London, 256 Gray' s Inn Road, London WC1X 8LD (United Kingdom); Kim, Hae-Won [Department of Nanobiomedical Science and WCU Research Center of Nanobiomedical Science, Dankook University, Chungnam 330-714 (Korea, Republic of); Institute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan 330-714 (Korea, Republic of); Department of Biomaterials Science, College of Dentistry, Dankook University, Cheonan 330-714 (Korea, Republic of); Gong, Myoung-Seon [Department of Nanobiomedical Science and WCU Research Center of Nanobiomedical Science, Dankook University, Chungnam 330-714 (Korea, Republic of); Institute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan 330-714 (Korea, Republic of); Knowles, Jonathan C. [Department of Nanobiomedical Science and WCU Research Center of Nanobiomedical Science, Dankook University, Chungnam 330-714 (Korea, Republic of); Division of Biomaterials and Tissue Engineering, Eastman Dental Institute, University College London, 256 Gray' s Inn Road, London WC1X 8LD (United Kingdom); Wall, Ivan B., E-mail: i.wall@ucl.ac.uk [Department of Nanobiomedical Science and WCU Research Center of Nanobiomedical Science, Dankook University, Chungnam 330-714 (Korea, Republic of); Department of Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE (United Kingdom)

    2013-05-01

    There is a continuing need to develop scaffold materials that can promote vascularisation throughout the tissue engineered construct. This study investigated the effect of cobalt oxide (CoO) doped into titanium phosphate glasses on material properties, biocompatibility and vascular endothelial growth factor (VEGF) secretion by osteoblastic MG63 cells. Glasses composed of (P{sub 2}O{sub 5}){sub 45}(Na{sub 2}O){sub 20}(TiO{sub 2}){sub 05}(CaO){sub 30−x}(CoO){sub x}(x = 0, 5, 10, and 15 mol%) were fabricated and the effect of Co on physicochemical properties including density, glass transition temperature (T{sub g}), degradation rate, ion release, and pH changes was assessed. The results showed that incorporation of CoO into the glass system produced an increase in density with little change in T{sub g}. It was then confirmed that the pH did not change significantly when CoO was incorporated in the glass, and stayed constant at around 6.5–7.0 throughout the dissolution study period of 336 h. Ion release results followed a specific pattern with increasing amounts of CoO. In general, although incorporation of CoO into a titanium phosphate glass increased its density, other bulk and surface properties of the glass did not show any significant changes. Cell culture studies performed using MG63 cells over a 7-day period indicated that the glasses provide a stable surface for cell attachment and are biocompatible. Furthermore, VEGF secretion was significantly enhanced on all glasses compared with standard tissue culture plastic and Co doping enhanced this effect further. In conclusion, the developed Co-doped glasses are stable and biocompatible and thus offer enhanced potential for engineering vascularized tissue. - Highlights: ► Phosphate-based glasses can be successfully doped with cobalt oxide. ► The resulting glass is highly stable with low degradation rate. ► Co-doped glasses are biocompatible but do not favour cell proliferation. ► Osteoblastic MG63 cells

  12. Infrared and Raman spectroscopic characterization of the phosphate mineral fairfieldite--Ca2(Mn2+,Fe2+)2(PO4)2·2(H2O).

    Science.gov (United States)

    Frost, Ray L; Xi, Yunfei; Scholz, Ricardo; Belotti, Fernanda Maria; Lopez, Andres

    2013-04-01

    Raman spectroscopy complimented with infrared spectroscopy has been used to determine the molecular structure of the phosphate mineral fairfieldite. The Raman phosphate (PO4)(3-) stretching region shows strong differences between the fairfieldite phosphate minerals which is attributed to the cation substitution for calcium in the structure. In the infrared spectra complexity exists with multiple (PO4)2- antisymmetric stretching vibrations observed, indicating a reduction of the tetrahedral symmetry. This loss of degeneracy is also reflected in the bending modes. Strong Raman bands around 600 cm(-1) are assigned to ν4 phosphate bending modes. Multiple bands in the 400-450 cm(-1) region assigned to ν2 phosphate bending modes provide further evidence of symmetry reduction of the phosphate anion. Three broadbands for fairfieldite are found at 3040, 3139 and 3271 cm(-1) and are assigned to OH stretching bands. By using a Libowitzky empirical equation hydrogen bond distances of 2.658 and 2.730Å are estimated. Vibrational spectroscopy enables aspects of the molecular structure of the fairfieldite to be ascertained. Copyright © 2013 Elsevier B.V. All rights reserved.

  13. Mineral resource assessment of rare-earth elements, thorium, titanium, and uranium in the Greenville 1 degree by 2 degrees Quadrangle, South Carolina, Georgia, and North Carolina

    Science.gov (United States)

    Lesure, Frank G.; Curtin, Gary C.; Daniels, David L.; Jackson, John C.

    1993-01-01

    Mineral resources of the Greenville 1° x 2° quadrangle, South Carolina, Georgia, and North Carolina, were assessed between 1984 and 1990 under the Conterminuous United States Mineral Assessment Program (CUSMAP) of the U.S. Geological Survey (USGS). The mineral resource assessments were made on the basis of geologic, geochemical, and geophysical investigations and the presence of mines, prospects, and mineral occurrences from the literature. This report is an assessment of the rare-earth elements (REE), thorium, titanium, and uranium resources in the Greenville quadrangle and is based on heavy mineral concentrates collected in 1951-54 by the USGS (Overstreet and others, 1968; Caldwell and White, 1973; Cuppels and White, 1973); on the results of the U.S. Department of Energy, National Uranium Resource Evaluation (NURE) sampling program (Ferguson, 1978, 1979); on analyses of stream-sediment and heavy-mineral-concentrate samples (Jackson and Moore, 1992, G.C Cullin, USGS, unpub. data, 1992) on maps showing aerial gamma radiation in the Greenville quadrangle (D.L. Daniels, USGS, unpub. data, 1992); and on the geology as mapped by Nelson and others (1987, 1989).

  14. The investigations of changes in mineral-organic and carbon-phosphate ratios in the mixed saliva by synchrotron infrared spectroscopy

    Science.gov (United States)

    Seredin, Pavel; Goloshchapov, Dmitry; Kashkarov, Vladimir; Ippolitov, Yuri; Bambery, Keith

    The objective of this study was to investigate the efficiency of the saturation of mixed saliva by mineral complexes and groups necessary for the remineralisation of tooth enamel using exogenous and endogenous methods of caries prevention. Using IR spectroscopy and high-intensity synchrotron radiation, changes in the composition of the human mixed saliva were identified when exogenous and endogenous methods of caries prevention are employed. Based on the calculations of mineral/organic and carbon/phosphate ratios, changes in the composition of the human mixed saliva depending on a certain type of prevention were identified. It is shown that the use of a toothpaste (exogenous prevention) alone based on a multi-mineral complex including calcium glycerophosphate provides only a short-term effect of saturating the oral cavity with mineral complexes and groups. Rinsing of the oral cavity with water following the preventive use of a toothpaste completely removes the effect of the saturation of the mixed saliva with mineral groups and complexes. The use of tablets of a multi-mineral complex with calcium glycerophosphate (endogenous prevention) in combination with exogenous prevention causes an average increase of ∼10% in the content of mineral groups and complexes in the mixed saliva and allows long-term saturation of the oral fluid by them. This method outperforms the exogenous one owing to a long-term effect of optimal concentrations of endogenous and biologically available derivatives of phosphates on the enamel surface.

  15. Fabrication of gelatin/calcium phosphate composite nanofibrous membranes by biomimetic mineralization.

    Science.gov (United States)

    Choi, Mi Ok; Kim, Young-Jin

    2012-06-01

    Based on the principles of biomimetic mineralization, biocomposite nanofibrous membranes were fabricated by the growth of CaP crystals on electrospun gelatin nanofibers to mimic both the physical architecture and chemical composition of natural bone ECM. Plenty more CaP crystals formed on the nanofibrous membrane containing Ca(2+) ion precursors, in which these crystals were also observed on the inner side of membrane. The release rate of Ca(2+) ion precursors from the nanofibrous membrane was slower than that of PO(4)(3-) ion precursors, suggesting the existence of more strong intermolecular interaction between gelatin and Ca(2+) ions. ATR-FTIR and XRD results clearly revealed the formation of CaP crystals mixed with apatite and CaCO(3), or apatite and TCP on the membranes. The Ca/P molar ratio of crystals obtained from the XPS data was 2.03 and 1.60, which depended on the mineralization conditions. Higher amount of CaP crystals significantly accelerated the deposit rate of bone-like apatite on the surface of composite membrane, meaning to the improved in vivo bone bioactivity.

  16. Micro-spectroscopic investigation of selenium-bearing minerals from the Western US Phosphate Resource Area

    Directory of Open Access Journals (Sweden)

    Gunter Mickey E

    2005-01-01

    Full Text Available Mining activities in the US Western Phosphate Resource Area (WPRA have released Se into the environment. Selenium has several different oxidation states and species, each having varying degrees of solubility, reactivity, and bioavailability. In this study we are investigating the speciation of Se in mine-waste rocks. Selenium speciation was determined using bulk and micro-x-ray absorption spectroscopy (XAS, as well as micro-x-ray fluorescence mapping. Rocks used for bulk-XAS were ground into fine powders. Shale used for micro-XAS was broken along depositional planes to expose unweathered surfaces. The near edge region of the XAS spectra (XANES for the bulk rock samples revealed multiple oxidation states, with peaks indicative of Se(-II, Se(IV, and Se(+VI species. Micro-XANES analysis of the shale indicated that three unique Se-bearing species were present. Using the XANES data together with ab initio fitting of the extended x-ray absorption fine structure region of the micro-XAS data (micro-EXAFS the three Se-bearing species were identified as dzharkenite, a di-selenide carbon compound, and Se-substituted pyrite. Results from this research will allow for a better understanding of the biogeochemical cycling of Se in the WPRA.

  17. Effect of phosphate buffer saline on coronal leakage of mineral trioxide aggregate.

    Science.gov (United States)

    Parirokh, Masoud; Askarifard, Sara; Mansouri, Shahla; Haghdoost, Ali A; Raoof, Maryam; Torabinejad, Mahmoud

    2009-06-01

    This study was carried out to compare the bacterial leakage of MTA used as a root-end filling material when it was kept in phosphate buffer saline (PBS) or normal saline. In this study, 72 freshly extracted teeth were used. The roots were randomly divided into four experimental groups of 15 each (groups I and II gutta-percha obturation + MTA, groups III and IV only MTA) and two positive and negative control groups of six each. The samples in groups I and III were kept in normal saline for 1 month while the samples in groups II and IV were kept in PBS. Enterococcus faecalis was used for determination of the bacterial penetration. Kaplan-Meier survival curve and chi(2) test were employed for data analysis. The obturated samples with root-end filling showed significantly longer duration of resistance to bacterial penetration than canals without obturation (P < 0.05). The roots that were placed in PBS (groups II and IV) showed significantly less bacterial penetration in comparison with the roots that were stored in normal saline (P < 0.05). In conclusion, MTA, which acts as a bioactive material, should be placed in a synthetic tissue fluid before any leakage evaluation.

  18. Influence Of Carboxymethyl Cellulose For The Transport Of Titanium Dioxide Nanoparticles In Clean Silica And Mineral-Coated Sands

    Science.gov (United States)

    The transport properties of titanium dioxide (anatase polymorph) nanoparticles encapsulated by carboxymethyl cellulose (CMC) were evaluated as a function of changes in the solute chemical properties in clean quartz, amorphous aluminum and iron hydroxide-coated sands. While prist...

  19. Goldquarryite, a new Cd-bearing phosphate mineral from the Gold Quarry mine, Eureka County, Nevada

    Science.gov (United States)

    Roberts, Andrew C.; Cooper, M.A.; Hawthorne, F.C.; Gault, Robert A.; Jensen, M.C.; Foord, E.E.

    2003-01-01

    Goldquarryite, idealized formula CuCd2Al3(PO44F2(H2O)10(H2O 2, structure-derived formula (Cu0.70???0.30??1.00(Cd1.68Ca0.32??2.00Al3 (PO44F2(H2O)10[(H2O 1.60F0.40]??2.00, is triclinic, space group P1, with unit-cell parameters derived from crystal structure: a = 6.787(1), b = 9.082(2), c = 10.113(2) A??, ?? = 101.40(1)??, ?? = 104.27(1)??, ?? = 102.51(1)??, V = 568.7(3) A??3, a:b:c: = 0.7473:1:1.1135, Z = 1. The strongest seven reflections in the X-ray powder-diffraction pattern are [d(A??)(I)(hkl)]: 9.433(100)(001); 4.726(30)(002); 3.700(30)(022); 3.173(30b)(122, 113, 120, 003); 3.010(30)(122, 212); 2.896(30)(211); 2.820(50)(022). The mineral occurs on a single specimen collected from the 5,425-foot bench, Gold Quarry mine, Eureka County, Nevada, as isolated clusters of radiating sprays of crystals and as compact parallel crystal aggregates, which are both found on and between breccia fragments. Sprays and aggregates never exceed 3 mm in longest dimension and typically average about 0.5 mm in size. Goldquarryite is a late-stage supergene mineral associated with opal, carbonate-fluorapatite and hewettite, on a host rock composed principally of brecciated and hydrothermally rounded jasperoid fragments which have been lightly cemented by late-stage silicification. Individual euhedral crystals are acicular to bladed, elongate [100], with a length-to-width ratio of approximately 20:1; the maximum size is 1.5 mm but most crystals do not exceed 0.4 mm in length. Forms are {010}, {001} major and {100} very minor. The mineral is pleochroic; translucent (masses) to transparent (crystals); very pale blue to blue-gray (crystals) or blue (masses); with a white streak and a vitreous to glassy luster. Goldquarryite is brittle, lacks cleavage, has an irregular fracture, and is nonfluorescent; hardness (Mohs') is estimated at 3-4; measured density is 2.78(1) g/cm3 (sink-float techniques using methylene iodide-acetone mixtures), calculated density is 2.81 g/cm3 (for formula and unit

  20. Experimetal research on comprehensive recovery of a low grade iron-titanium-phosphate ore in Chengde%承德某低品位铁钛磷矿综合回收试验研究

    Institute of Scientific and Technical Information of China (English)

    唐平宇; 王素; 田江涛

    2012-01-01

    Aimed at the low grade iron-titanium-phosphate ore in chengde comprehensive recovery test research,using low intensity magnetic separation iron,flotation election phosphorus,high intensity magnetic-flotation recovery of ilmenite combined process. In the election of iron at the same time, comprehensive recovery phosphate, titanium associated elements, respectively to obtain a qualified iron phosphate titanium concentrate product, achieved the desired technical indicators, improve resource utilization and economic benefits,in order to chengde regions of the development and utilization of the same type ore deposits provide the technical basis.%针对承德某低品位铁钛磷矿石进行了综合回收试验研究,采用弱磁选铁、浮选选磷、强磁-浮选回收钛铁矿的联合工艺流程.在选铁同时,综合回收磷、钛伴生元素,分别获得合格的铁磷钛精矿产品,取得了理想的技术指标,提高了资源利用率和综合经济效益,为承德地区同类型矿床的开发利用提供了技术依据.

  1. Investigation of the growth and local stoichiometric point group symmetry of titania nanotubes during potentiostatic anodization of titanium in phosphate electrolytes

    Science.gov (United States)

    Cummings, F. R.; Muller, T. F. G.; Malgas, G. F.; Arendse, C. J.

    2015-10-01

    Potentiostatic anodization of commercially pure, 50 μm-thick titanium (Ti) foil was performed in aqueous, phosphate electrolytes at increasing experimental timeframes at a fixed applied potential for the synthesis of titania nanotube arrays (TNAs). High resolution scanning electron microscopy images, combined with energy dispersive spectroscopy and x-ray diffraction spectra reveal that anodization of the Ti foil in a 1 M NaF+0.5 M H3PO4 electrolyte for 4 h yields a titanate surface with pore diameters ranging between 100 and 500 nm. The presence of rods on the Ti foil surface with lengths exceeding 20 μm and containing high concentrations of phosphor on the exterior was also detected at these conditions, along with micro-sized coral reef-like titanate balls. We propose that the formation of these structures play a major role during the anodization process and impedes nanotube growth during the anodization process. High spatially resolved scanning transmission electron microscopy-electron energy loss spectroscopy (STEM-EELS) performed along the length of a single anodized TiO2 nanotube reveals a gradual evolution of the nanotube crystallinity, from a rutile-rich bottom to a predominantly anatase TiO2 structure along its length.

  2. A vibrational spectroscopic study of the phosphate mineral whiteite CaMn++Mg2Al2(PO4)4(OH)2 8(H2O).

    OpenAIRE

    Frost, Ray L.; Sholz, Ricardo Augusto; López, Andrés; Xi, Yunfei

    2014-01-01

    Vibrational spectroscopy enables subtle details of the molecular structure of whiteite to be determined. Single crystals of a pure phase from a Brazilian pegmatite were used. The infrared and Raman spectroscopy were applied to compare the molecular structure of whiteite with that of other phosphate minerals. The Raman spectrum of whiteite shows an intense band at 972 cm_1 assigned to the m1 PO3_ 4 symmetric stretching vibrations. The low intensity Raman bands at 1076 and 1173 cm_1 are assigne...

  3. Effect of Thymosin beta4 on the Differentiation and Mineralization of MC3T3-E1 Cell on a Titanium Surface.

    Science.gov (United States)

    Jeong, Soon-Jeong; Jeong, Moon-Jin

    2016-02-01

    Osteoblasts are responsible for the synthesis of bone matrix through the secretion of collagenous and non-collagenous proteins with mineralization. Thymosin beta4 (Tbeta4) is an actin-sequestering peptide that is involved in the regulation of cell proliferation, differentiation and motility. A recent study reported that the inhibition of Tbeta4 mRNA synthesis strongly decreases the level of gene expression of bone sialoprotein (BSP), dentin sialophosphoprotein (DSPP), osteocalcin (OCN), osteonectin (ON) and collagen type I (Col I) with mineralization during differentiation in odontoblasts. Titanium (Ti) is used commonly as an implant material for dental implants, which have strong mechanical potential and good biocompatibility with bone. This study examined whether Tbeta4 can be a potential molecule for promoting the differentiation and mineralization of MC3T3-E1 cells on a Ti surface. Tbeta4 increased the viability of MC3T3-E1 cells during differentiation on Ti discs compared to that of the control. The expression of Tbeta4 mRNA and protein in the Tbeta4-treated MC3T3-E1 cells was higher than the control during differentiation on the Ti discs. In addition, Tbeta4 increased the formation of mineralization nodules and the mRNA expression of alkaline phosphatase (ALP), DSPP, dentin matrix protein1 (DMP1), BSP and Col I compared to that of the control in MC3T3-E1 cells during differentiation on Ti discs. From the results, Tbeta4 increased the viability and promoted the differentiation and mineralization of MC3T3-E1 cells on Ti discs. This highlights the potential use of Tbeta4 for increasing osseointegration through osteoblast differentiation and mineralization on Ti discs.

  4. Synthesis of a novel organic-inorganic hybrid of polyaniline/titanium phosphate for Re(VII) removal.

    Science.gov (United States)

    Gao, Yang; Chen, Changlun; Chen, He; Zhang, Rui; Wang, Xiangke

    2015-05-21

    The organic-inorganic hybrid material of polyaniline/titanium(IV) (PANI/Ti(HPO4)2) was synthesized by an oxidative polymerization reaction. The PANI/Ti(HPO4)2 was applied to remove Re(VII). The size of Ti(HPO4)2 nanoplates has no obvious effect on the sorption capacity. The effects of various environmental factors (such as pH, extra anions (NO3(-) and MO4(2-)) and temperature) on Re(VII) sorption to PANI/Ti(HPO4)2 were investigated by batch experiments. The sorption kinetics followed a pseudo-second-order model. The nitrogen-containing functional groups of PANI promoted Re(VII) sorption. The PANI/Ti(HPO4)2 exhibited excellent maximum sorption capacity to Re(VII) (47.62 mg g(-1)), which was superior to that of PANI (10.75 mg g(-1)) and much higher than that of many other sorbents. The sorption isotherms of Re(VII) can be well fitted with the Langmuir model. Re(VII) sorption decreased with increasing solution pH at pH > 4.0, which implied that Re(VII) sorption on PANI/Ti(HPO4)2 might be attributed to the outer-sphere complexation between amine and imine groups on the surface of PANI/Ti(HPO4)2 and Re(VII). This study implies that the hybrid material of PANI/Ti(HPO4)2 can be regarded as a potential sorbent to remove Re(VII) and its analogues from large volumes of aqueous solutions.

  5. In-situ mineralization of chitosan/calcium phosphate composite and the effect of solvent on the structure

    Science.gov (United States)

    He, Ling-Hao; Yao, Lu; Xue, Rui; Sun, Jing; Song, Rui

    2011-09-01

    Solvent played an important role in the formation of calcium phosphate phase of the chitosan/calcium phosphate composites. In this investigation, ethanolacetic acid mixtures were employed as solvents, and various calcium phosphate phases, such as brushite, amorphous calcium phosphate, and hydroxyapatite, were introduced into the chitosan/calcium phosphate composites by using in-situ preparation process. The results showed that the structures of composite were influenced remarkably by the morphology and the distribution of calcium phosphate phase. In addition, the bioactivity of composites was governed mainly by the characters of calcium phosphate phases in composites, since calcium phosphate phases could induce the growth of hydroxyapatite coating on the surfaces of composites. On the surface of chitosan/brushite composite, the formed hydroxyapatite coating consisted of oriented plate crystallites, which selfassembled into spherical-like crystals. When other calcium phosphate phase was introduced into composites, the polymorphs of hydroxyapatite layer would change greatly. The oriented plate crystallites became bigger, and meanwhile, the self-assembled aggregates became less and smaller. In addition, with the shift of the prior nucleating point, the growth orientation of plate crystallites was transformed.

  6. Vibrational spectroscopic characterization of the phosphate mineral ludlamite (Fe,Mn,Mg)3(PO4)2ṡ4H2O - A mineral found in lithium bearing pegmatites

    Science.gov (United States)

    Frost, Ray L.; Xi, Yunfei; Scholz, Ricardo; Belotti, Fernanda M.

    2013-02-01

    The objective of this work is to analyze ludlamite (Fe,Mn,Mg)3(PO4)2ṡ4H2O from Boa Vista mine, Galiléia, Brazil and to assess the molecular structure of the mineral. The phosphate mineral ludlamite has been characterized by EMP-WDS, Raman and infrared spectroscopic measurements. The mineral is shown to be a ferrous phosphate with some minor substitution of Mg and Mn. Raman bands at 917 and 950 cm-1 are assigned to the symmetric stretching mode of HOPO32- and PO43- units. Raman bands at 548, 564, 599 and 634 cm-1 are assigned to the ν4PO43- bending modes. Raman bands at 2605, 2730, 2896 and 3190 cm-1 and infrared bands at 2623, 2838, 3136 and 3185 cm-1 are attributed to water stretching vibrations. By using a Libowitzky empirical function, hydrogen bond distances are calculated from the OH stretching wavenumbers. Strong hydrogen bonds in the structure of ludlamite are observed as determined by their hydrogen bond distances. The application of infrared and Raman spectroscopy to the study of ludlamite enables the molecular structure of the pegmatite mineral ludlamite to be assessed.

  7. Molecular structure of the phosphate mineral brazilianite NaAl3(PO4)2(OH)4 - A semi precious jewel

    Science.gov (United States)

    Frost, Ray L.; Xi, Yunfei

    2012-02-01

    The phosphate mineral brazilianite NaAl3(PO4)2(OH)4 is a semi precious jewel. There are almost no minerals apart from brazilianite which are used in jewellery. Vibrational spectroscopy was used to characterise the molecular structure of brazilianite. Brazilianite is composed of chains of edge-sharing Al-O octahedra linked by P-O tetrahedra, with Na located in cavities of the framework. An intense sharp Raman band at 1019 cm-1 is attributed to the PO43- symmetric stretching mode. Raman bands at 973 and 988 cm-1 are assigned to the stretching vibrations of the HOPO33- units. The infrared spectra compliment the Raman spectra but show greater complexity. Multiple Raman bands are observed in the PO43- and HOPO33- bending region. This observation implies that both phosphate and hydrogen phosphate units are involved in the structure. Raman OH stretching vibrations are found at 3249, 3417 and 3472 cm-1. These peaks show that the OH units are not equivalent in the brazilianite structure. Vibrational spectroscopy is useful for increasing the knowledge of the molecular structure of brazilianite.

  8. Vibrational spectroscopic characterization of the phosphate mineral kulanite Ba(Fe(2+),Mn(2+),Mg)2(Al,Fe(3+))2(PO4)3(OH)3.

    Science.gov (United States)

    Frost, Ray L; López, Andrés; Xi, Yunfei; Granja, Amanda; Scholz, Ricardo

    2013-11-01

    The mineral kulanite BaFe2Al2(PO4)3(OH)3, a barium iron aluminum phosphate, has been studied by using a combination of electron microscopy and vibrational spectroscopy. Scanning electron microscopy with EDX shows the mineral is homogenous with no other phases present. The Raman spectrum is dominated by an intense band at 1022cm(-1) assigned to the PO4(3-)ν1 symmetric stretching mode. Low intensity Raman bands at 1076, 1110, 1146, 1182cm(-1) are attributed to the PO4(3-)ν3 antisymmetric stretching vibrations. The infrared spectrum shows a complex spectral profile with overlapping bands. Multiple phosphate bending vibrations supports the concept of a reduction in symmetry of the phosphate anion. Raman spectrum at 3211, 3513 and 3533cm(-1) are assigned to the stretching vibrations of the OH units. Vibrational spectroscopy enables aspects on the molecular structure of kulanite to be assessed. Copyright © 2013 Elsevier B.V. All rights reserved.

  9. Minerals

    Directory of Open Access Journals (Sweden)

    Vaquero, M. P.

    1998-08-01

    Full Text Available The possible changes in the mineral composition of food during frying could be the consequence of losses by leaching, or changes in concentrations caused by exchanges between the food and culinary fat of other compounds. The net result depends on the type of food, the frying fat used and the frying process. Moreover, the modifications that frying produces in other nutrients could indirectly affect the availability of dietary minerals. The most outstanding ones are those that can take place in the fat or in the protein. With respect to the interactions between frying oils and minerals, we have recent knowledge concerning the effects of consuming vegetable oils used in repeated fryings of potatoes without turnover, on the nutritive utilization of dietary minerals. The experiments have been carried out in pregnant and growing rats, which consumed diets containing, as a sole source of fat, the testing frying oils or unused oils. It seems that the consumption of various frying oils, with a polar compound content lower or close to the maximum limit of 25% accepted for human consumption, does not alter the absorption and metabolism of calcium, phosphorous, iron or copper. Magnesium absorption from diets containing frying oils tends to increase but the urinary excretion of this element increases, resulting imperceptible the variations in the magnesium balance. The urinary excretion of Zn also increased although its balance remained unchanged. Different studies referring to the effects of consuming fried fatty fish on mineral bioavailability will also be presented. On one hand, frying can cause structural changes in fish protein, which are associated with an increase in iron absorption and a decrease in body zinc retention. The nutritive utilization of other elements such as magnesium, calcium and copper seems to be unaffected. On the other hand; it has been described that an excess of fish fatty acids in the diet produces iron depletion, but when fatty

  10. SEM-EDX, Raman and infrared spectroscopic characterization of the phosphate mineral frondelite (Mn2+)(Fe3+)4(PO4)3(OH)5.

    Science.gov (United States)

    Frost, Ray L; Xi, Yunfei; Scholz, Ricardo; Belotti, Fernanda M; Beganovic, Martina

    2013-06-01

    We have analyzed a frondelite mineral sample from the Cigana mine, located in the municipality of Conselheiro Pena, a well-known pegmatite in Brazil. In the Cigana pegmatite, secondary phosphates, namely eosphorite, fairfieldite, fluorapatite, frondelite, gormanite, hureaulite, lithiophilite, reddingite and vivianite are common minerals in miarolitic cavities and in massive blocks after triphylite. The chemical formula was determined as (Mn0.68, Fe0.32)(Fe(3+))3,72(PO4)3.17(OH)4.99. The structure of the mineral was assessed using vibrational spectroscopy. Bands attributed to the stretching and bending modes of PO4(3-) and HOPO3(3-) units were identified. The observation of multiple bands supports the concept of symmetry reduction of the phosphate anion in the frondelite structure. Sharp Raman and infrared bands at 3581 cm(-1) is assigned to the OH stretching vibration. Broad Raman bands at 3063, 3529 and 3365 cm(-1) are attributed to water stretching vibrational modes. Copyright © 2013 Elsevier B.V. All rights reserved.

  11. Effects of sintering temperature on surface morphology/microstructure, in vitro degradability, mineralization and osteoblast response to magnesium phosphate as biomedical material.

    Science.gov (United States)

    Wang, Zhiwei; Ma, Yuhai; Wei, Jie; Chen, Xiao; Cao, Liehu; Weng, Weizong; Li, Quan; Guo, Han; Su, Jiacan

    2017-04-11

    Magnesium phosphate (MP) was fabricated using a chemical precipitation method, and the biological performances of MP sintered at different temperatures as a biomedical material was investigated. The results indicated that the densification and crystallinity of MP increased as the sintering temperature increased. As the sintering temperature increased, the degradability of MP in PBS decreased, and the mineralization ability in SBF significantly increased. In addition, the MP sintered at 800 °C (MP8) possessed the lowest degradability and highest mineralization ability. Moreover, the positive response of MG63 cells to MP significantly increased as the sintering temperature increased, and MP8 significantly promoted the cell spreading, proliferation, differentiation and expressions of osteogenic differentiation-related genes. Faster degradation of MP0 resulted in higher pH environments and ion concentrations, which led to negative responses to osteoblasts. However, the appropriate degradation of MP8 resulted in suitable pH environments and ion concentrations, which led to positive responses to osteoblasts. This study demonstrated that the sintering temperature substantially affected the surface morphology/microstructure, degradability and mineralization, and osteoblasts response to magnesium phosphate.

  12. Breket titanium (Titanium bracket

    Directory of Open Access Journals (Sweden)

    Sianiwati Goenharto

    2005-09-01

    Full Text Available There has been a considerable discussion in the literature about corrosion and sensitivity to the nickel present in stainless steel brackets. Titanium has been heralded as a material totally compatible in the oral environment and superior in structural integrity compared to stainless steel. Many current applications in dentistry and medicine have made titanium an obvious choice for a possible substitute material. Titanium based brackets have shown excellent corrosion resistance and possessed good biocompatibility. Evaluation of titanium brackets for orthodontic therapy showed that titanium brackets were comparable to stainless steel brackets in passive and active configuration. Study about metallographic structure, hardness, bond strength to enamel substrate, etc. showed that titanium brackets exhibited a potential for clinical application. It was concluded that titanium brackets were suitable substitute for stainless steel brackets.

  13. Raman spectroscopic study of the mineral qingheiite Na2(Mn2+,Mg,Fe2+)2(Al,Fe3+)(PO4)3, a pegmatite phosphate mineral from Santa Ana pegmatite, Argentina

    Science.gov (United States)

    Frost, Ray L.; Xi, Yunfei; Scholz, Ricardo; López, Andrés; Moreira, Caio; de Lena, Jorge Carvalho

    2013-10-01

    The pegmatite mineral qingheiite Na2(Mn2+,Mg,Fe2+)2(Al,Fe3+)(PO4)3 has been studied by a combination of SEM and EMP, Raman and infrared spectroscopy. The studied sample was collected from the Santa Ana pegmatite, Argentina. The mineral occurs as a primary mineral in lithium bearing pegmatite, in association with beausite and lithiophilite. The Raman spectrum is characterized by a very sharp intense Raman band at 980 cm-1 assigned to the PO43- symmetric stretching mode. Multiple Raman bands are observed in the PO43- antisymmetric stretching region, providing evidence for the existence of more than one phosphate unit in the structure of qingheiite and evidence for the reduction in symmetry of the phosphate units. This concept is affirmed by the number of bands in the ν4 and ν2 bending regions. No intensity was observed in the OH stretching region in the Raman spectrum but significant intensity is found in the infrared spectrum. Infrared bands are observed at 2917, 3195, 3414 and 3498 cm-1 are assigned to water stretching vibrations. It is suggested that some water is coordinating the metal cations in the structure of qingheiite.

  14. Mineralization of soluble P fertilizers and insoluble rock phosphate in response to phosphate-solubilizing bacteria and poultry manure and their effect on the growth and P utilization efficiency of chilli (Capsicum annuum L.)

    Science.gov (United States)

    Abbasi, M. K.; Musa, N.; Manzoor, M.

    2015-08-01

    The ability of soil microorganisms and organic manure to convert insoluble phosphorus (P) to an accessible form offers a biological rescue system for improving P utilization efficiency in soil-plant systems. Our objective was to examine the P mineralization potential of two soluble P fertilizers (SPF), i.e., single superphosphate (SSP) and diammonium phosphate (DAP), and of insoluble rock phosphate (RP) with and without phosphate-solubilizing bacteria (PSB) and poultry manure (PM) and their subsequent effect on the growth, yield and P utilization efficiency (PUE) of chilli (Capsicum annuum L.). An incubation study was carried out on a loam (slightly alkaline) soil with 12 treatments: T0 - control; T1 - RP; T2 - SSP; T3 - DAP; T4 - PM; T5 - 1/2 RP+1/2 SSP; T6 - 1/2 RP+1/2 DAP; T7 - 1/2 RP+1/2 PM; T8 - RP+PSB; T9 - 1/2 RP+1/2 SSP+PSB; T10 - 1/2 RP+1/2 DAP+PSB; and T11 - 1/2 RP+1/2 PM+PSB. Phosphorus mineralization was measured by analyzing extractable P from the amended soil incubated under controlled conditions at 25 °C for periods of 0, 5, 15, 25, 35 and 60 days. A complementary greenhouse experiment was conducted in pots with chilli (Capsicum annuum L.) as a test crop. Growth, yield, P uptake and PUE of the chilli was determined during the study. Results indicated that P mineralization in soil amended with RP was 6.0-11.5 mg kg-1, while both soluble P fertilizers resulted in 68-73 mg P kg-1 at day 0, which decreased by 79-82 % at the end of incubation. The integrated use of PSB and PM with RP in T11 stimulated P mineralization by releasing a maximum of 25 mg P kg-1 that was maintained at high levels without any loss. Use of PSB decreased soil pH. In the greenhouse experiment, RP alone or RP+PSB did not have a significant impact on plant growth. However, the combined use of RP, PM and PSB in T11 resulted in similar growth, yield and P uptake of chilli as DAP. The PUE of applied P varied from 4 to 29 % and was higher in the treatments that included PSB. We conclude

  15. Electrospinning of calcium phosphate-poly (d,l-lactic acid) nanofibers for sustained release of water-soluble drug and fast mineralization.

    Science.gov (United States)

    Fu, Qi-Wei; Zi, Yun-Peng; Xu, Wei; Zhou, Rong; Cai, Zhu-Yun; Zheng, Wei-Jie; Chen, Feng; Qian, Qi-Rong

    Calcium phosphate-based biomaterials have been well studied in biomedical fields due to their outstanding chemical and biological properties which are similar to the inorganic constituents in bone tissue. In this study, amorphous calcium phosphate (ACP) nanoparticles were prepared by a precipitation method, and used for preparation of ACP-poly(d,l-lactic acid) (ACP-PLA) nanofibers and water-soluble drug-containing ACP-PLA nanofibers by electrospinning. Promoting the encapsulation efficiency of water-soluble drugs in electrospun hydrophobic polymer nanofibers is a common problem due to the incompatibility between the water-soluble drug molecules and hydrophobic polymers solution. Herein, we used a native biomolecule of lecithin as a biocompatible surfactant to overcome this problem, and successfully prepared water-soluble drug-containing ACP-PLA nanofibers. The lecithin and ACP nanoparticles played important roles in stabilizing water-soluble drug in the electrospinning composite solution. The electrospun drug-containing ACP-PLA nanofibers exhibited fast mineralization in simulated body fluid. The ACP nanoparticles played the key role of seeds in the process of mineralization. Furthermore, the drug-containing ACP-PLA nanofibers exhibited sustained drug release which simultaneously occurred with the in situ mineralization in simulated body fluid. The osteoblast-like (MG63) cells with spreading filopodia were well observed on the as-prepared nanofibrous mats after culturing for 24 hours, indicating a high cytocompatibility. Due to the high biocompatibility, sustained drug release, and fast mineralization, the as-prepared composite nanofibers may have potential applications in water-soluble drug loading and release for tissue engineering.

  16. Electrospinning of calcium phosphate-poly (d,l-lactic acid) nanofibers for sustained release of water-soluble drug and fast mineralization

    Science.gov (United States)

    Fu, Qi-Wei; Zi, Yun-Peng; Xu, Wei; Zhou, Rong; Cai, Zhu-Yun; Zheng, Wei-Jie; Chen, Feng; Qian, Qi-Rong

    2016-01-01

    Calcium phosphate-based biomaterials have been well studied in biomedical fields due to their outstanding chemical and biological properties which are similar to the inorganic constituents in bone tissue. In this study, amorphous calcium phosphate (ACP) nanoparticles were prepared by a precipitation method, and used for preparation of ACP-poly(d,l-lactic acid) (ACP-PLA) nanofibers and water-soluble drug-containing ACP-PLA nanofibers by electrospinning. Promoting the encapsulation efficiency of water-soluble drugs in electrospun hydrophobic polymer nanofibers is a common problem due to the incompatibility between the water-soluble drug molecules and hydrophobic polymers solution. Herein, we used a native biomolecule of lecithin as a biocompatible surfactant to overcome this problem, and successfully prepared water-soluble drug-containing ACP-PLA nanofibers. The lecithin and ACP nanoparticles played important roles in stabilizing water-soluble drug in the electrospinning composite solution. The electrospun drug-containing ACP-PLA nanofibers exhibited fast mineralization in simulated body fluid. The ACP nanoparticles played the key role of seeds in the process of mineralization. Furthermore, the drug-containing ACP-PLA nanofibers exhibited sustained drug release which simultaneously occurred with the in situ mineralization in simulated body fluid. The osteoblast-like (MG63) cells with spreading filopodia were well observed on the as-prepared nanofibrous mats after culturing for 24 hours, indicating a high cytocompatibility. Due to the high biocompatibility, sustained drug release, and fast mineralization, the as-prepared composite nanofibers may have potential applications in water-soluble drug loading and release for tissue engineering. PMID:27785016

  17. Carbon nanotubes/pectin/minerals substituted apatite nanocomposite depositions on anodized titanium for hard tissue implant: In vivo biological performance{sup †}

    Energy Technology Data Exchange (ETDEWEB)

    Govindaraj, Dharman [Biomaterials in Medicinal Chemistry Lab, Department of Natural Products Chemistry, School of Chemistry, Madurai Kamaraj University, Madurai 625021 (India); Rajan, Mariappan, E-mail: rajanm153@gmail.com [Biomaterials in Medicinal Chemistry Lab, Department of Natural Products Chemistry, School of Chemistry, Madurai Kamaraj University, Madurai 625021 (India); Munusamy, Murugan A.; Alarfaj, Abdullah A. [Department of Botany and Microbiology, College of Science, King Saud University, Riyadh (Saudi Arabia); Higuchi, Akon [Department of Chemical and Materials Engineering, National Central University, Jhong-li, Taoyuan, 32001 Taiwan (China); Suresh Kumar, S. [Department of Medical Microbiology and Parasitology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang (Malaysia)

    2017-06-15

    A surface deposition approach enveloping the use of biocompatible trace components and strengthening materials will affect the physicochemical and osseointegration properties of nanocomposite deposited implants. The current work is aimed at the development of functionalized carbon nanotubes (f-CNT)/Pectin (P)/mineralized hydroxyapatite (M-HA) ((f-CNT/P/M-HA)) nanocomposite depositions by electrophoretic deposition on anodized titanium (TiO{sub 2}) implant. The capacity of f-CNT manages the cost of mechanical strength, while pectin (extracted from pomegranate peel) and minerals (strontium, magnesium, and zinc) enhance the biocompatibility of the HA deposition was investigate utilizing different methods. The functional and morphological analyses were done by FTIR, XRD, XPS, SEM-EDX and TEM. The mechanical depiction results show improved adherence quality for the nanocomposite deposition. Additionally, an enhanced viability of osteoblast cells (MG63 (HOS)) was monitored in vitro on the f-CNT/P/M-HA nanocomposite deposition. The capacity of the nanocomposite deposited TiO{sub 2} implant to encourage bone development was assessed in vivo. Hence, the as-synthesized nanocomposite deposited TiO{sub 2} that joins the comfort osteoconductivity of mineralized hydroxyapatite, pectin collectively with the compressive strength of f-CNT can have numerous uses in orthopaedics since it could enhance implant fixation in human bone. - Highlights: • Successful development of CNTs–Pectin reinforced M-HA nanocomposite coating on TiO{sub 2} by electrodeposition. • The success of nanocomposite coatings was evidenced with FTIR, XRD, XPS, SEM-EDX, and TEM. • Nanocomposite coating on TiO{sub 2} is bio-resistive, better candidate for implant applications. • The fabricate nanocomposite coatings showed good biocompatibility and no adverse effect from in vitro and in vivo tests.

  18. Surface induced reactivity for titanium by ion implantation.

    Science.gov (United States)

    Pham, M T; Reuther, H; Matz, W; Mueller, R; Steiner, G; Oswald, S; Zyganov, I

    2000-06-01

    Calcium and phosphorus storage in a thin layer of titanium surface was achieved by ion implantation. We study the reactivity of this surface in response to a hydrothermal treatment. The incipient implanted species are observed to convert to Ca(2+) and PO(4)(3-), the precursors for generating calcium phosphate polymorphs. Hydroxyapatite is formed from these precursors by an interface-liquid mediated mineralization preceded by the hydrolysis of oxygen compounds of Ca and P from the solid phase. The morphology and organization of apatite mineral is controlled by the fluid dynamics reflecting the surface remodeling to adapt to the available local environment. Exposed to calcium and phosphate ion containing solution, the hydrothermally treated surface templates hydroxyapatite deposition. Ca and P implanted Ti surface was shown to be chemically and morphologically actively involved in the interfacial reactions.

  19. Origin and nature of the aluminium phosphate-sulfate minerals (APS associated with uranium mineralization in triassic red-beds (Iberian Range, Spain

    Directory of Open Access Journals (Sweden)

    Marfil, R.

    2013-06-01

    Full Text Available This study focuses on the mineralogical and chemical study of an Aluminium–phosphate–sulphate (APS mineralization that occurs in a clastic sequence from the Triassic (Buntsandstein of the Iberian Range. The deposit is constituted by sandstones, mudstones, and conglomerates with arenaceous matrix, which were deposited in fluvial to shallow-marine environments. In addition to APS minerals, the following diagenetic minerals are present in the clastic sequence: quartz, K-feldspar, kaolinite group minerals, illite, Fe-oxides-hidroxides, carbonate-sulphate cement-replacements and secondary uraniferous minerals. APS minerals were identified and characterized by optical microscopy, X-ray diffraction, scanning electron microscopy, and electron microprobe. Microcrystalline APS crystals occur replacing uraniferous minerals, associated with kaolinite, mica and filling pores, in distal fluvial-to-tidal arkoses-subarkoses. Given their Ca, Sr, and Ba contents, the APS minerals can be defined as a solid solution of crandallite-goyacite-gorceixite (0.53 Ca, 0.46 Sr and 0.01 Ba. The chemical composition, low LREE concentration and Sr > S suggest that the APS mineral were originated during the supergene alteration of the Buntsandstein sandstones due to the presence of the mineralizing fluids which causes the development of U-bearing sandstones in a distal alteration area precipitating from partially dissolved and altered detrital minerals. Besides, the occurrence of dickite associated with APS minerals indicates they were precipitated at diagenetic temperatures (higher than 80ºC, related to the uplifting occurred during the late Cretaceous post-rift thermal stage.Este trabajo se centra en el estudio de los minerales fosfato-sulfato alumínicos (APS que se producenen una secuencia clástica del Triásico (Buntsandstein de la Cordillera Ibérica. El depósito está constituido por areniscas, lutitas y conglomerados con matriz arenosa, que fueron depositados en

  20. Pegmatito Gentil (Mendes Pimentel, MG) e suas paragêneses mineralógicas de fosfatos raros Gentil Pegmatite (Mendes Pimentel, MG) and their rare phosphate mineral assemblages

    OpenAIRE

    Mario Luiz de Sá C. Chaves; Ricardo Scholz

    2008-01-01

    Centenas de corpos pegmatíticos na região nordeste de Minas Gerais produzem minerais gemológicos e de coleção, muitos desses corpos possuindo afinidades com determinada espécie, grupo ou classe mineral. O Pegmatito Gentil em Mendes Pimentel, ora descrito, notabiliza-se por sua assembléia de minerais fosfáticos, a maior parte dos quais raros ou raríssimos na natureza. A associação mineral identificada inclui microclínio, quartzo, muscovita, almandina-espessartita, berilo e trifilita como fosfa...

  1. The therapeutic effect on bone mineral formation from biomimetic zinc containing tricalcium phosphate (ZnTCP) in zinc-deficient osteoporotic mice.

    Science.gov (United States)

    Chou, Joshua; Hao, Jia; Hatoyama, Hirokazu; Ben-Nissan, Besim; Milthorpe, Bruce; Otsuka, Makoto

    2013-01-01

    The aim of this study was to evaluate the therapeutic efficacy of biomimetic zinc-containing tricalcium phosphate (ZnTCP) produced by hydrothermally converting calcium carbonate exoskeletons from foraminifera, in the treatment of osteoporotic mice. X-Ray powder diffraction showed crystallographic structures matching JCPDS profile for tricalcium phosphate. Mass spectroscopy used to calculate total composition amount showed similar amount of calcium (5×10(4) µg/g) and phosphate (4×10(4) ppm) after conversion and the presence of zinc (5.18×10(3) µg/g). In vitro zinc release showed no release in PBS buffer and <1% zinc release in 7 days. In vivo evaluation was done in ovariectomized mice by implanting the ZnTCP samples in the soft tissues near the right femur bone for four weeks. Thirty ddY mice (5 weeks old, average weight of 21 g) were divided into six experimental groups (normal, sham, OVX, β-TCP, ZnTCP and direct injection of zinc). CT images were taken every two weeks where the bone mineral density (BMD) and bone mineral content (BMC) were calculated by software based on CT images. The ZnTCP group exhibits cortical and cancellous bone growth of 45% and 20% respectively. While sham, OVX and β-TCP suffered from bone loss. A correlation was made between the significant body weight increase in ZnTCP with the significant increase in plasma zinc level compared with OVX. The presented results indicate that biomimetic ZnTCP were effective in preventing and treating bone loss in osteoporotic mice model.

  2. The therapeutic effect on bone mineral formation from biomimetic zinc containing tricalcium phosphate (ZnTCP in zinc-deficient osteoporotic mice.

    Directory of Open Access Journals (Sweden)

    Joshua Chou

    Full Text Available The aim of this study was to evaluate the therapeutic efficacy of biomimetic zinc-containing tricalcium phosphate (ZnTCP produced by hydrothermally converting calcium carbonate exoskeletons from foraminifera, in the treatment of osteoporotic mice. X-Ray powder diffraction showed crystallographic structures matching JCPDS profile for tricalcium phosphate. Mass spectroscopy used to calculate total composition amount showed similar amount of calcium (5×10(4 µg/g and phosphate (4×10(4 ppm after conversion and the presence of zinc (5.18×10(3 µg/g. In vitro zinc release showed no release in PBS buffer and <1% zinc release in 7 days. In vivo evaluation was done in ovariectomized mice by implanting the ZnTCP samples in the soft tissues near the right femur bone for four weeks. Thirty ddY mice (5 weeks old, average weight of 21 g were divided into six experimental groups (normal, sham, OVX, β-TCP, ZnTCP and direct injection of zinc. CT images were taken every two weeks where the bone mineral density (BMD and bone mineral content (BMC were calculated by software based on CT images. The ZnTCP group exhibits cortical and cancellous bone growth of 45% and 20% respectively. While sham, OVX and β-TCP suffered from bone loss. A correlation was made between the significant body weight increase in ZnTCP with the significant increase in plasma zinc level compared with OVX. The presented results indicate that biomimetic ZnTCP were effective in preventing and treating bone loss in osteoporotic mice model.

  3. Electrospinning of calcium phosphate-poly(D,L-lactic acid nanofibers for sustained release of water-soluble drug and fast mineralization

    Directory of Open Access Journals (Sweden)

    Fu QW

    2016-10-01

    Full Text Available Qi-Wei Fu,1,* Yun-Peng Zi,1,* Wei Xu,1 Rong Zhou,1 Zhu-Yun Cai,1 Wei-Jie Zheng,1 Feng Chen,2 Qi-Rong Qian1 1Department of Orthopedics, Changzheng Hospital, Second Military Medical University, 2State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, People’s Republic of China *These authors contributed equally to this work Abstract: Calcium phosphate-based biomaterials have been well studied in biomedical fields due to their outstanding chemical and biological properties which are similar to the inorganic constituents in bone tissue. In this study, amorphous calcium phosphate (ACP nanoparticles were prepared by a precipitation method, and used for preparation of ACP-poly(D,L-lactic acid (ACP-PLA nanofibers and water-soluble drug-containing ACP-PLA nanofibers by electrospinning. Promoting the encapsulation efficiency of water-soluble drugs in electrospun hydrophobic polymer nanofibers is a common problem due to the incompatibility between the water-soluble drug molecules and hydrophobic polymers solution. Herein, we used a native biomolecule of lecithin as a biocompatible surfactant to overcome this problem, and successfully prepared water-soluble drug-containing ACP-PLA nanofibers. The lecithin and ACP nanoparticles played important roles in stabilizing water-soluble drug in the electrospinning composite solution. The electrospun drug-containing ACP-PLA nanofibers exhibited fast mineralization in simulated body fluid. The ACP nanoparticles played the key role of seeds in the process of mineralization. Furthermore, the drug-containing ACP-PLA nanofibers exhibited sustained drug release which simultaneously occurred with the in situ mineralization in simulated body fluid. The osteoblast-like (MG63 cells with spreading filopodia were well observed on the as-prepared nanofibrous mats after culturing for 24 hours, indicating a high cytocompatibility. Due

  4. Interactions between supplemented mineral phosphorus and phytase on phytate hydrolysis and inositol phosphates in the small intestine of broilers1,2.

    Science.gov (United States)

    Zeller, Ellen; Schollenberger, Margit; Witzig, Maren; Shastak, Yauheni; Kühn, Imke; Hoelzle, Ludwig E; Rodehutscord, Markus

    2015-05-01

    Phytate breakdown in the digestive tract of broilers is affected by supplements of mineral phosphorus (P) and phytase with unknown interactions between the 2 factors. It was the objective to study phytate hydrolysis and the presence of inositol phosphate isomers (InsPs) as affected by supplements of mineral P and phytase in the small intestine of broilers. Fifteen-day old broilers were assigned to 48 pens of 20 broilers each (n = 8 pens/treatment). Two low-P corn-soybean meal-based diets without (BD-; 4.4 g P/kg dry matter) or with monocalcium phosphate (MCP; BD+; 5.2 g P/kg dry matter) were supplied without or with added phytase at 500 or 12,500 FTU/kg. On d 24, digesta from the duodenum/jejunum and lower ileum was pooled per segment on a by-pen basis, freeze-dried, and analyzed for P, InsPs, and the marker TiO2. Another 180 broilers (n = 6 pens/treatment, 10 birds each) were fed the 3 BD+ diets from d 1 to 21 to assess the influence of supplemented phytase on tibia mineralization and strength. Significant interactions between MCP and phytase supplements on myo-inositol 1,2,3,4,5,6-hexakis (dihydrogen phosphate) (InsP6) hydrolysis (duodenum/jejunum: P ≤ 0.001; ileum: P = 0.004) and level of specific lower InsPs were detected. Supplementation with 12,500 FTU/kg phytase resulted in 92% InsP6 hydrolysis and strong degradation of InsP5. This treatment resulted in higher P net absorption, affirmed by higher BW gain, tibia strength, and mineralization compared to treatments without or with 500 FTU/kg phytase (P ≤ 0.05). MCP supplementation reduced the degradation of InsP6 and specific lower InsPs in birds fed diets without or with 500 FTU/kg of phytase (P ≤ 0.05), but did not reduce InsP6 hydrolysis or degradation of InsP5 at the high phytase dose. Effects of added MCP on phytase efficacy depend on the dose of supplemented phytase. Differences in the concentrations of lower InsPs indicated that the initial step of InsP6 hydrolysis is not the only

  5. A Raman spectroscopic study of the mono-hydrogen phosphate mineral dorfmanite Na 2(PO 3OH)·2H 2O and in comparison with brushite

    Science.gov (United States)

    Frost, Ray L.; Palmer, Sara J.; Xi, Yunfei

    2011-11-01

    Aspects of the molecular structure of the mineral dorfmanite Na 2(PO 3OH)·2H 2O were determined by Raman spectroscopy. The mineral originated from the Kedykverpakhk Mt., Lovozero, Kola Peninsula, Russia. Raman bands are assigned to the hydrogen phosphate units. The intense Raman band at 949 cm -1 and the less intense band at 866 cm -1 are assigned to the PO 3 and POH stretching vibrations. Bands at 991, 1066 and 1141 cm -1 are assigned to the ν3 antisymmetric stretching modes. Raman bands at 393, 413 and 448 cm -1 and 514, 541 and 570 cm -1 are attributed to the ν2 and ν4 bending modes of the HPO 4 units, respectively. Raman bands at 3373, 3443 and 3492 cm -1 are assigned to water stretching vibrations. POH stretching vibrations are identified by bands at 2904, 3080 and 3134 cm -1. Raman spectroscopy has proven very useful for the study of the structure of the mineral dorfmanite.

  6. Mineral-nitrogen leaching and ammonia volatilization from a rice-rapeseed system as affected by 3,4-dimethylpyrazole phosphate.

    Science.gov (United States)

    Li, Hua; Chen, Yingxu; Liang, Xinqiang; Lian, Yanfeng; Li, Wenhong

    2009-01-01

    3,4-Dimethylpyrazole phosphate (DMPP) was validated as an effective nitrification inhibitor to reduce nitrate leaching. Its effects on ammonia (NH(3)) volatilization were not clear, especially on farmland scale with crop rotations. In this study, on-farm experiments at the Jiaxing (JX) and Yuhang (YH) sites in Taihu Lake Basin, China were conducted to evaluate the effect of DMPP application on mineral nitrogen (N) (NH(4)-N and NO(3)-N) leaching and NH(3) volatilization losses in a rice-rapeseed cropping system. Treatments included urea alone (UA), urea + 1% DMPP (UD), and no fertilizer (CK). The results show that DMPP reduced NO(3)-N leaching fluxes by 44.9 to 59.9% and increased NH(4)-N leaching fluxes by 13.0 to 33.3% at two sites during rice and rape seasons compared with urea alone. Reductions in mineral-N leaching fluxes by DMPP in two seasons at the JX and YH sites were 9.5 and 14.3 kg N ha(-1), respectively, compared with UA treatment. The application of DMPP had no significant effects on NH(3) volatilization loss fluxes at either site. The rice and rapeseed yields were 5.3 to 7.4% higher in UD plots than in UA plots at two sites. These results that indicate DMPP could reduce leaching losses of mineral-N from crop fields and promote grain yields by conserving more applied N in soil in rice-rapeseed rotation systems.

  7. COMBINED BIOLOGICAL-PHOTOCATALYTIC TREATMENT FOR THE MINERALIZATION OF A MIXTURE OF CHLOROPHENOLS IN AN ELECTROLYTE-CONTAINING MODEL WATER AND SPONTANEOUS SEDIMENTATION OF TITANIUM DIOXIDE

    Directory of Open Access Journals (Sweden)

    Dhanus Suryaman

    2010-06-01

    Full Text Available To shorten the biological treating time and to examine the effect of electrolytes in a model water on the photocatalytic treatment, the combined biological-photocatalytic treatment was evaluated for removal of a mixture (total: 100 mg L-1, each: 25 mg L-1 of 2-chlorophenol (2-CP, 2,4-dichlorophenol (2,4-DCP, 2,4,5-trichlorophenol (2,4,5-TCP, and pentachlorophenol (PCP in tap water. The mineralization of the four phenols was performed by a flow (biological treatment-circulative flow (photocatalytic treatment operation under black light and sunlight irradiations. After a large portion of biodegradable 2-CP and 2,4-DCP, and around half amount of slightly biodegradable 2,4,5-TCP were removed by the biological treatment, the remained three chlorophenols, biorecalcitrant PCP, and  biodegradation products were completely removed by the subsequent photocatalytic treatment. The combined treatment significantly shortened the degradation time only the biotreatment. High circulative flow rate (600 mL min-1 enabled for TiO2 particles to completely suspend in a tubular photoreactor and resulted in high removals of chlorophenols and TOC. Sunlight irradiation was successfully used and the saving of the electric energy of black light was possible. Since TiO2 particles in the tap water spontaneously sedimented on standing after the photocatalytic treatment, the combined system can be operated by integrating it with the TiO2 separation.   Keywords: photocatalysis, titanium dioxide, biodegradation, pollutant, wastewater

  8. Repression of mineral phosphate solubilizing phenotype in the presence of weak organic acids in plant growth promoting fluorescent pseudomonads.

    Science.gov (United States)

    Patel, Divya K; Murawala, Prayag; Archana, G; Kumar, G Naresh

    2011-02-01

    Two phosphate solubilizing bacteria (PSB), M3 and SP1, were obtained from the rhizosphere of mungbean and sweet potato, respectively and identified as strains of Pseudomonas aeruginosa. Their rock phosphate (RP) solubilizing abilities were found to be due to secretion high amount of gluconic acid. In the presence of malate and succinate, individually and as mixture, the P solubilizing ability of both the strains was considerably reduced. This was correlated with a nearly 80% decrease in the activity of the glucose dehydrogenase (GDH) but not gluconate dehydrogenase (GAD) in both the isolates. Thus, GDH enzyme, catalyzing the periplasmic production of gluconic acid, is under reverse catabolite repression control by organic acids in P. aeruginosa M3 and SP1. This is of relevance in rhizospheric conditions and is a new explanation for the lack of field efficacy of such PSB.

  9. Titanium metal: extraction to application

    Energy Technology Data Exchange (ETDEWEB)

    Gambogi, Joseph (USGS, Reston, VA); Gerdemann, Stephen J.

    2002-09-01

    In 1998, approximately 57,000 tons of titanium metal was consumed in the form of mill products (1). Only about 5% of the 4 million tons of titanium minerals consumed each year is used to produce titanium metal, with the remainder primarily used to produce titanium dioxide pigment. Titanium metal production is primarily based on the direct chlorination of rutile to produce titanium tetrachloride, which is then reduced to metal using the Kroll magnesium reduction process. The use of titanium is tied to its high strength-to-weight ratio and corrosion resistance. Aerospace is the largest application for titanium. In this paper, we discuss all aspects of the titanium industry from ore deposits through extraction to present and future applications. The methods of both primary (mining of ore, extraction, and purification) and secondary (forming and machining) operations will be analyzed. The chemical and physical properties of titanium metal will be briefly examined. Present and future applications for titanium will be discussed. Finally, the economics of titanium metal production also are analyzed as well as the advantages and disadvantages of various alternative extraction methods.

  10. Beta-tricalcium phosphate, white mineral trioxide aggregate, white Portland cement, ferric sulfate, and formocresol used as pulpotomy agents in primary pig teeth.

    Science.gov (United States)

    Shayegan, Amir; Petein, Michel; Abbeele, Astrid Vanden

    2008-04-01

    The purpose of this study was to evaluate and compare the effects of formocresol (FC), ferric sulfate (FS), white mineral trioxide aggregate (WMTA), white Portland cement (WPC), and beta-tricalcium phosphate (beta-TCP) on pulpotomized primary teeth of pigs. Fifty teeth of three 3-month old pigs were pulpotomized with these materials. Three weeks later, the animals were euthanized and the specimens were prepared for histological examination. There was no significant difference between beta-TCP, WMTA, and WPC in terms of primary pulp response, hard tissue formation, and normal pulp tissue preservation. But, both FS and FC irritated the pulp tissue, provoking a more inflammatory pulp response than beta-TCP, WMTA, and WPC. Beta-TCP, WMTA, and WPC are histologically more effective pulpotomy agents than formocresol and ferric sulfate in primary pig teeth.

  11. Raman and infrared spectroscopic characterization of the phosphate mineral paravauxite Fe2+Al2(PO4)2(OH)2.8H2O.

    Science.gov (United States)

    Frost, Ray L; Scholz, Ricardo; Lópes, Andrés; Xi, Yunfei; Gobac, Zeljka Žigovečki; Horta, Laura Frota Campos

    2013-12-01

    We have undertaken a vibrational spectroscopic study of paravauxite the Siglo XX mine, Bustillo Province, northern of Potosí department, Bolivia. This mine is important source for rare and unusual secondary phosphate minerals and is the type locality for a number of rare phosphates such as vauxite, sigloite, metavauxite and for jeanbandyite. The chemical formula of the studied sample was determined as Fe(2+)(0.9)5, Al(0.07)Σ1.02 (Al)2.09 (PO4)1:97 (OH)1.98 · 7.90(H2O). The Raman spectrum is dominated by an intense Raman band at 1020 cm(-1) assigned to the PO4(3-) ν1 symmetric stretching mode. Low intensity Raman bands found at 1058, 1115 and 1148 cm(-1) are assigned to the PO4(3-) ν3 antisymmetric stretching vibrations. Raman bands of paravauxite at 537, 570, 609 and 643 cm(-1) are assigned to the ν4 PO4(3-) bending modes whilst the Raman bands at 393 and 420 cm(-1) are due to the ν2 PO4(3-) bending modes. The Raman spectral profile of paravauxite in the hydroxyl stretching region is broad with component bands resolved at 3086, 3215, 3315, 3421, 3505 and 3648 cm(-1). Vibrational spectroscopy enables the assessment of the molecular structure of paravauxite to be undertaken. Copyright © 2013 Elsevier B.V. All rights reserved.

  12. Efficacy of reactive mineral-based sorbents for phosphate, bacteria, nitrogen and TOC removal--column experiment in recirculation batch mode.

    Science.gov (United States)

    Nilsson, Charlotte; Lakshmanan, Ramnath; Renman, Gunno; Rajarao, Gunaratna Kuttuva

    2013-09-15

    Two mineral-based materials (Polonite and Sorbulite) intended for filter wells in on-site wastewater treatment were compared in terms of removal of phosphate (PO4-P), total inorganic nitrogen (TIN), total organic carbon (TOC) and faecal indicator bacteria (Escherichia coli and Enterococci). Using an innovative, recirculating system, septic tank effluent was pumped at a hydraulic loading rate of 3000 L m(2) d(-1) into triplicate bench-scale columns of each material over a 90-day period. The results showed that Polonite performed better with respect to removal of PO4-P, retaining on average 80% compared with 75% in Sorbulite. This difference was attributed to higher CaO content in Polonite and its faster dissolution. Polonite also performed better in terms of removal of bacteria because of its higher pH value. The total average reduction in E. coli was 60% in Polonite and 45% in Sorbulite, while for Enterococci the corresponding value was 56% in Polonite and 34% in Sorbulite. Sorbulite removed TIN more effectively, with a removal rate of 23%, while Polonite removed 11% of TIN, as well as TOC. Organic matter (measured as TOC) was accumulated in the filter materials but was also released periodically. The results showed that Sorbulite could meet the demand in removing phosphate and nitrogen with reduced microbial release from the wastewater treatment process.

  13. Purification and identification of O-GlcNAc-modified peptides using phosphate-based alkyne CLICK chemistry in combination with titanium dioxide chromatography and mass spectrometry

    DEFF Research Database (Denmark)

    Parker, Benjamin L; Gupta, Pankaj; Cordwell, Stuart

    2011-01-01

    -containing peptides were enriched using titanium dioxide chromatography. Modified peptides were analyzed using a combination of higher energy collision dissociation for identification and electron transfer dissociation to localize the site of O-GlcNAc attachment. The enrichment method was developed...

  14. Influence of Irradiance, Flow Rate, Reactor Geometry, and Photopromoter Concentration in Mineralization Kinetics of Methane in Air and in Aqueous Solutions by Photocatalytic Membranes Immobilizing Titanium Dioxide

    Directory of Open Access Journals (Sweden)

    Ignazio Renato Bellobono

    2008-01-01

    Full Text Available Photomineralization of methane in air (10.0–1000 ppm (mass/volume of C at 100% relative humidity (dioxygen as oxygen donor was systematically studied at 318±3 K in an annular laboratory-scale reactor by photocatalytic membranes immobilizing titanium dioxide as a function of substrate concentration, absorbed power per unit length of membrane, reactor geometry, and concentration of a proprietary vanadium alkoxide as photopromoter. Kinetics of both substrate disappearance, to yield intermediates, and total organic carbon (TOC disappearance, to yield carbon dioxide, were followed. At a fixed value of irradiance (0.30 W⋅cm-1, the mineralization experiments in gaseous phase were repeated as a function of flow rate (4–400 m3⋅h−1. Moreover, at a standard flow rate of 300 m3⋅h−1, the ratio between the overall reaction volume and the length of the membrane was varied, substantially by varying the volume of reservoir, from and to which circulation of gaseous stream took place. Photomineralization of methane in aqueous solutions was also studied, in the same annular reactor and in the same conditions, but in a concentration range of 0.8–2.0 ppm of C, and by using stoichiometric hydrogen peroxide as an oxygen donor. A kinetic model was employed, from which, by a set of differential equations, four final optimised parameters, k1 and K1, k2 and K2, were calculated, which is able to fit the whole kinetic profile adequately. The influence of irradiance on k1 and k2, as well as of flow rate on K1 and K2, is rationalized. The influence of reactor geometry on k values is discussed in view of standardization procedures of photocatalytic experiments. Modeling of quantum yields, as a function of substrate concentration and irradiance, as well as of concentration of photopromoter, was carried out very satisfactorily. Kinetics of hydroxyl radicals reacting between themselves, leading to hydrogen peroxide, other than with substrate or

  15. Distribution of Some Elements in Biosubstrates of Workers Occupied in the Production of Mineral Nitrogenous Phosphate Fertilizers

    CERN Document Server

    Gorbunov, A V; Lyapunov, S M; Okina, O I; Pavlov, S S; Geological Institute RAS, Moscow, Russia

    2005-01-01

    The data on the content of some trace elements typical for the production of nitrogenous phosphate fertilizers (F, Sr, rare-earth elements), as well as heavy and toxic metals in industrial products, occupational air, drinking water and biosubstrates (urine, hair) of the factory workers are presented. The correlations between the content of fluorine in urine and hair of workers and between the content of fluorine, length of service and age, have been shown. The correlation dependence between the content of F in biosubstrates and a number of trace elements typical for the given type of production has been evaluated. The comparison of the morbidity and character of diseases of the factory workers and of the local residents unoccupied in the production has been made.

  16. Low cost titanium--myth or reality

    Energy Technology Data Exchange (ETDEWEB)

    Turner, Paul C.; Hartman, Alan D.; Hansen, Jeffrey S.; Gerdemann, Stephen J.

    2001-01-01

    In 1998, approximately 57,000 tons of titanium metal was consumed in the form of mill products (1). Only about 5% of the 4 million tons of titanium minerals consumed each year is used to produce titanium metal, with the remainder primarily used to produce titanium dioxide pigment. Titanium metal production is primarily based on the direct chlorination of rutile to produce titanium tetrachloride, which is then reduced to metal using the Kroll magnesium reduction process. The use of titanium is tied to its high strength-to-weight ratio and corrosion resistance. Aerospace is the largest application for titanium, and titanium cost has prevented its use in non-aerospace applications including the automotive and heavy vehicle industries.

  17. Accessing alkali-free NASICON-type compounds through mixed oxoanion sol-gel chemistry: Hydrogen titanium phosphate sulfate, H1-xTi2(PO4)3-x(SO4)x (x=0.5-1)

    Science.gov (United States)

    Mieritz, Daniel; Davidowski, Stephen K.; Seo, Dong-Kyun

    2016-10-01

    We report a direct sol-gel synthesis and characterization of new proton-containing, rhombohedral NASICION-type titanium compounds with mixed phosphate and sulfate oxoanions. The synthetic conditions were established by utilizing peroxide ion as a decomposable and stabilizing ligand for titanyl ions in the presence of phosphates in a strong acidic medium. Thermogravimetric analysis (TGA), powder X-ray diffraction (PXRD), induction-coupled plasma optical emission spectroscopic (ICP-OES) elemental analysis, and Raman and 1H magic angle spinning nuclear magnetic resonance (MAS-NMR) spectroscopic studies have determined the presence of sulfate and proton ions in the structure, for which the compositional range has been found to be H1-xTi2(PO4)3-x(SO4)x (x=0.5-1). The particulate products exhibit a nanocrystalline nature observed through characterization with scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The N2 sorption isotherm measurements and subsequent Brunauer-Emmett-Teller (BET) and Barrett-Joyner-Halenda (BJH) analyses confirmed the presence of the textural meso- and macropores in the materials. Future studies would determine the potential of the new compounds in various applications as battery materials, proton conductors and solid acid catalysts.

  18. Influence of MgO on mineral structure and metallurgical properties of blast furnace slag with medium titanium%MgO对中钛型高炉渣矿相结构及冶金性能的影响

    Institute of Scientific and Technical Information of China (English)

    邓美乐; 韩秀丽; 刘磊; 张玓; 李运刚

    2016-01-01

    The mineral structure of blast furnace slag containing medium titanium with different mass percent of MgO (7%-16%) was studied by means of polarization microscope.The results show that the texture of the slag was porphyritic. the mineral compositions are mainly the rich titanium diopside and melilite,followed by spinel,perovskite,titanau-gite,and finally a little of metallic iron,titanium nitride,titanium carbide and their solid solution. As the mass percent of MgO increased,the content of the perovskite and the rich titanium diopside reduced first and then increased,the con-tents of the titanaugite increased gradually and the contents of the melilite increased first and then decreased. When the mass percent of MgO reached 14%,The first phase of the high-melting spinel appeared,which resulted in higher vos-cosity and melting temperature of blast furnace slag,and the liquidity of blast furnace slag also became worse. The above results have a vital guiding significance on improving the liquidity of blast furnace slag with medium titanium.%采用偏光显微镜对不同MgO质量分数(7%~16%)条件下中钛型高炉渣的矿相结构进行研究。结果表明,炉渣显微结构为斑状结构、似斑状结构;矿物组成主要为巴依石、黄长石,其次为尖晶石、钙钛矿、钛辉石,少量的金属铁、氮化钛、碳化钛及其固溶体;随着MgO质量分数的增加,炉渣中钙钛矿及巴依石质量分数先降低后升高,钛辉石质量分数逐渐升高,而黄长石质量分数先升高后降低;当MgO质量分数达到14%时,出现了第一期尖晶石这种高熔点化合物,会导致炉渣的黏度和熔化温度升高,炉渣的流动性变坏。该研究成果对改善中钛型高炉渣的流动性能具有重要指导意义。

  19. A minimum 2-year comparative study of autologous cancellous bone grafting versus beta-tricalcium phosphate in anterior cervical discectomy and fusion using a rectangular titanium stand-alone cage.

    Science.gov (United States)

    Yamagata, Toru; Naito, Kentaro; Arima, Hironori; Yoshimura, Masaki; Ohata, Kenji; Takami, Toshihiro

    2016-07-01

    Although titanium stand-alone cages are commonly used in anterior cervical discectomy and fusion (ACDF), there are several concerns such as cage subsidence after surgery. The efficacy of β-tricalcium phosphate (β-TCP) granules as a packing material in 1- or 2-level ACDF using a rectangular titanium stand-alone cage is not fully understood. The purpose of this study is to investigate the validity of rectangular titanium stand-alone cages in 1- and 2-level ACDF with β-TCP. This retrospective study included 55 consecutive patients who underwent ACDF with autologous iliac cancellous bone grafting and 45 consecutive patients with β-TCP grafting. All patients completed at least 2-year postoperative follow-up. Univariate and multivariate analyses were performed to examine the associations between study variables and nonunion after surgery. Significant neurological recovery after surgery was obtained in both groups. Cage subsidence was noted in 14 of 72 cages (19.4 %) in the autograft group and 12 of 64 cages (18.8 %) in the β-TCP group. A total of 66 cages (91.7 %) in the autograft group showed osseous or partial union, and 58 cages (90.6 %) in the β-TCP group showed osseous or partial union by 2 years after surgery. There were no significant differences in cage subsidence and the bony fusion rate between the two groups. Multivariate analysis using a logistic regression model showed that fusion level at C6/7, 2-level fusion, and cage subsidence of grades 2-3 were significantly associated with nonunion at 2 years after surgery. Although an acceptable surgical outcome with negligible complication appears to justify the use of rectangular titanium stand-alone cages in 1- and 2-level ACDF with β-TCP, cage subsidence after surgery needs to be avoided to achieve acceptable bony fusion at the fused segments. Fusion level at C6/7 or 2-level fusion may be another risk factor of nonunion.

  20. Phosphate binder pill burden, patient-reported non-adherence, and mineral bone disorder markers: Findings from the DOPPS.

    Science.gov (United States)

    Fissell, Rachel B; Karaboyas, Angelo; Bieber, Brian A; Sen, Ananda; Li, Yun; Lopes, Antonio A; Akiba, Takashi; Bommer, Jürgen; Ethier, Jean; Jadoul, Michel; Pisoni, Ronald L; Robinson, Bruce M; Tentori, Francesca

    2016-01-01

    Because of multiple comorbidities, hemodialysis (HD) patients are prescribed many oral medications, including phosphate binders (PBs), often resulting in a high "pill burden." Using data from the international Dialysis Outcomes and Practice Patterns Study (DOPPS), we assessed associations between PB pill burden, patient-reported PB non-adherence, and levels of serum phosphorus (SPhos) and parathyroid hormone (PTH) using standard regression analyses. The study included data collected from 5262 HD patients from dialysis units participating in the DOPPS in 12 countries. PB prescription ranged from a mean of 7.4 pills per day in the United States to 3.9 pills per day in France. About half of the patients were prescribed at least 6 PB pills per day, and 13% were prescribed at least 12 PB pills per day. Overall, the proportion of patients who reported skipping PBs at least once in the past month was 45% overall, ranging from 33% in Belgium to 57% in the United States. There was a trend toward greater PB non-adherence and a higher number of prescribed PB pills per day. Non-adherence to PB prescription was associated with high SPhos (>5.5 mg/dL) and PTH (>600 pg/mL). Adherence to PB is a challenge for many HD patients and may be related to the number of PB pills prescribed. Prescription of a simplified PB regimen could improve patient adherence and perhaps improve SPhos and PTH levels. © 2015 International Society for Hemodialysis.

  1. Differentiation of osteoblasts on pectin-coated titanium.

    Science.gov (United States)

    Kokkonen, H; Cassinelli, C; Verhoef, R; Morra, M; Schols, H A; Tuukkanen, J

    2008-09-01

    The gold standard for implant metals is titanium, and coatings such as collagen-I, RGD-peptide, chondroitin sulfate, and calcium phosphate have been used to modify its biocompatibility. We investigated how titanium coated with pectins, adaptable bioactive plant polysaccharides with anti-inflammatory effects, supports osteoblast differentiation. MC3T3-E1 cells, primary murine osteoblasts, and human mesenchymal cells (hMC) were cultured on titanium coated with rhamnogalacturonan-rich modified hairy regions (MHR-A and MHR-B) of apple pectin. Alkaline phosphatase (ALP) expression and activity, calcium deposition, and cell spreading were investigated. MHR-B, but not MHR-A, supports osteoblast differentiation. The MHR-A surface was not mineralized, but on MHR-B, the average mineralized area was 14.0% with MC3T3-E1 cells and 26.6% with primary osteoblasts. The ALP activity of hMCs on MHR-A was 58.3% at day 7 and 9.3% from that of MHR-B at day 10. These data indicate that modified pectin nanocoatings may enhance the biocompatibility of bone and dental implants.

  2. Electrolytic deposition of calcium phosphate/chitosan coating on titanium alloy: Growth kinetics and influence of current density, acetic acid, and chitosan

    NARCIS (Netherlands)

    Wang, Jiawei; Apeldoorn, van Aart; Groot, de Klaas

    2006-01-01

    Electrolytically deposited calcium phosphate/chitosan coating demonstrated good bone marrow stromal cell attachment. The aim of this study was to understand the coating's growth kinetics as well as the effects of current density, acetic acid, and chitosan on the coating's formation. The scanning ele

  3. Increased osteoinductivity and mineralization by minimal concentration of bone morphogenetic protein-2 loaded onto biphasic calcium phosphate in a rabbit sinus

    Science.gov (United States)

    2016-01-01

    Purpose The purpose of the present study was to evaluate the effectiveness of a minimal concentration of bone morphogenetic protein-2 (BMP-2) in terms of quantitative and qualitative analyses of newly formed bone in a rabbit maxillary sinus model. Methods In 7 rabbits, sinus windows were prepared bilaterally. Biphasic calcium phosphate (BCP) loaded with 0.05 mg/mL BMP-2 was grafted into one sinus (the BMP group) and saline-soaked BCP was placed into the other (the control group) in each animal. The animals were allowed an 8-week healing period before being sacrificed. Specimens including the augmented area and surrounding tissues were then removed and evaluated both radiographically and histologically. Results There was a difference in the mineralization of new bone between the groups. In the BMP group, the greater part of the new bone consisted of mature lamellar bone with an evident trabecular pattern, whereas the control group showed mostly woven bone, consisting only partially of lamellar bone. Histometrically, the area of new bone was significantly greater (4.55±1.35 mm2 vs. 2.99±0.86 mm2) in the BMP group than in the control group (Pmineralization in a rabbit sinus model using a BCP carrier. PMID:27800217

  4. Bone Formation with Deproteinized Bovine Bone Mineral or Biphasic Calcium Phosphate in the Presence of Autologous Platelet Lysate: Comparative Investigation in Rabbit

    Directory of Open Access Journals (Sweden)

    Carole Chakar

    2014-01-01

    Full Text Available Bone substitutes alone or supplemented with platelet-derived concentrates are widely used to promote bone regeneration but their potency remains controversial. The aim of this study was, therefore, to compare the regenerative potential of preparations containing autologous platelet lysate (APL and particles of either deproteinized bovine bone mineral (DBBM or biphasic calcium phosphate (BCP, two bone substitutes with different resorption patterns. Rabbit APL was prepared by freeze-thawing a platelet suspension. Critical-size defects in rabbit femoral condyle were filled with DBBM or DBBM+APL and BCP or BCP+APL. Rabbits were sacrificed after six weeks and newly formed bone and residual implanted material were evaluated using nondemineralized histology and histomorphometry. New bone was observed around particles of all fillers tested. In the defects filled with BCP, the newly formed bone area was greater (70%; P<0.001 while the residual material area was lower (60%; P<0.001 than that observed in those filled with DBBM. New bone and residual material area of defects filled with either APL+DBBM or APL+BCP were similar to those observed in those filled with the material alone. In summary, osteoconductivity and resorption of BCP were greater than those of DBBM, while APL associated with either DBBM or BCP did not have an additional benefit.

  5. 钛合金表面氟化物-磷酸盐转化膜的制备及性能研究%Preparation and Properties of Fluoride-Phosphate Conversion Coating Formed on Titanium Alloy

    Institute of Scientific and Technical Information of China (English)

    叶君; 杜楠; 王力强; 尹茂生; 周国华; 王帅星

    2015-01-01

    目的:研究一种钛合金化学转化工艺,增强钛合金表面防护能力及其与涂层的结合能力。方法通过单因素实验确定TC1钛合金氟化物-磷酸盐转化工艺,采用SEM,EDS,XRD分析膜层的微观形貌及成分,同时测试转化膜的有关性能。结果在Na3 PO440 g/L,NaF 15 g/L,酸度调节剂A 25 mL/L,pH控制在4.4~4.6之间,温度30益条件下,可在TC1钛合金表面获得均匀一致的灰色转化膜。转化膜由许多细小的球状晶粒组成,主要相成分为Na3 TiOF5及Na2 TiF6。转化膜的摩擦系数仅为0.3~0.5,明显低于TC1基体。转化膜与TB06-9底漆的干性附着力为0级,浸泡48 h后的湿态附着力仍可达1级,远远好于TC1基体。结论氟化物-磷酸盐转化膜可以降低TC1钛合金的摩擦系数,提高其与有机涂层的附着力。%ABSTRACT:Objective A chemical conversion technique was researched to enhance the protective ability of titanium alloy surface and the adhesion between titanium alloy and organic coating. Methods The preparation technique of fluoride-phosphate conversion coating formed on TC1 alloy was determined by the single-factor experiments. The microstructure and composition of conversion coating were analyzed by SEM, EDS and XRD. Besides, the related properties of the conversion coating were researched. Results A uniform, coherent and gray conversion coating could be obtained on the surface of TC1 alloy when Na3 PO4 , NaF, Acidity Regu-lator A, pH and temperature were 40 g/L, 15 g/L, 25 mL/L, 4. 4~4. 6 and 30 ℃, respectively. The microstructure of the coa-ting showed many small spherical grains. The main phase components were Na3 TiOF5 and Na2 TiF6 . The friction coefficient of the fluoride-phosphate conversion coating was only 0. 3~0. 5, which was significantly lower than that of TC1 alloy. The dry adhesion level between conversion coating and TB06-9 organic coating was 0, and the wet adhesion level after 48 h immersion could still reach 1, both were far

  6. Sub-stoichiometric titanium oxide (Ti4O7) as a suitable ceramic anode for electrooxidation of organic pollutants: A case study of kinetics, mineralization and toxicity assessment of amoxicillin.

    Science.gov (United States)

    Ganiyu, Soliu O; Oturan, Nihal; Raffy, Stéphane; Cretin, Marc; Esmilaire, Roseline; van Hullebusch, Eric; Esposito, Giovanni; Oturan, Mehmet A

    2016-12-01

    Electrochemical degradation of aqueous solutions containing antibiotic amoxicillin (AMX) has been extensively studied in an undivided electrolytic cell using a sub-stoichiometric titanium oxide (Ti4O7) anode, elaborated by plasma deposition. Oxidative degradation of AMX by hydroxyl radicals was assessed as a function of applied current and was found to follow pseudo-first order kinetics. The use of carbon-felt cathode enhanced oxidation capacity of the process due to the generation of H2O2. Comparative studies at low current intensity using dimensional stable anode (DSA) and Pt anodes led to the lower mineralization efficiencies compared to Ti4O7 anode: 36 and 41% TOC removal for DSA and Pt respectively compared to 69% for Ti4O7 anode. Besides, the use of boron doped diamond (BDD) anode under similar operating conditions allowed reaching higher mineralization (94%) efficiency. Although Ti4O7 anode provides a lesser mineralization rate compared to BDD, it exhibits better performance compared to the classical anodes Pt and DSA and can constitutes an alternative to BDD anode for a cost effective electro-oxidation process. Moreover several aromatic and aliphatic oxidation reaction intermediates and inorganic end-products were identified and a plausible mineralization pathway of AMX involving these intermediates was proposed. Copyright © 2016 Elsevier Ltd. All rights reserved.

  7. Characterization of Hydroxyapatite Film on Titanium Substrate by Sputtering Technique

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    Radiofrequent magnetron sputtering technique was used to produce calcium phosphate coated on the titanium substrates, and the sputtered coating films were crystallized in an autoclave at 110 ℃ using a low temperature hydrothermal technique. The crystallization of as- sputtered coating film on the titanium substrates were amorphous calcium phosphate film. However, after the hydrothermal technique, calcium phosphate crystals grew and these were columnar crystal. The Ca/ P ratio of sputtered coating films in 1.6 to 2.0.

  8. Carriers in mesenchymal stem cell osteoblast mineralization-State-of-the-art

    DEFF Research Database (Denmark)

    Dahl, Morten; Jørgensen, Niklas Rye; Hørberg, Mette

    2014-01-01

    PURPOSE: Tissue engineering is a new way to regenerate bone tissue, where osteogenic capable cells combine with an appropriate scaffolding material. Our aim was in a Medline Search to evaluate osteoblast mineralization in vitro and in vivo including gene expressing combining mesenchymal stem cells......, on mineralization and gene expression. ß-tricalcium phosphate (ß-TCP) revealed elevated alkaline phosphatase activity, and calcium-deficient hydroxyapatite a greater gene expression of osteocalcin when seeded with induced MSCs. CONCLUSION: No data are published on titanium used as a carrier in MSC osteoblast...

  9. Microstructure and Characteristics of Calcium Phosphate Layers on Bioactive Oxide Surfaces of Air-Sintered Titanium Foams after Immersion in Simulated Body Fluid

    Directory of Open Access Journals (Sweden)

    Hung-Bin Lee

    2016-11-01

    Full Text Available We propose a simple and low-cost process for the preparation of porous Ti foams through a sponge replication method using single-step air sintering at various temperatures. In this study, the apatite-forming ability of air-sintered Ti samples after 21 days of immersion in simulated body fluid (SBF was investigated. The microstructures of the prepared Ca–P deposits were examined by X-ray diffraction (XRD, field-emission scanning electron microscopy (FE-SEM, Fourier transform infrared (FTIR spectroscopy, and cross-sectional transmission electron microscopy (TEM. In contrast to the control sample sintered in vacuum, which was found to have the simple hexagonal α-Ti phase, the air-sintered samples contained only the rutile phase. High intensities of XRD peaks for rutile TiO2 were obtained with samples sintered at 1000 °C. Moreover, the air-sintered Ti samples had a greater apatite-forming ability than that of the Ti sample sintered in vacuum. Ti samples sintered at 900 and 1000 °C had large aggregated spheroidal particles on their surfaces after immersion in SBF for 21 days. Combined XRD, energy-dispersive X-ray spectroscopy, FTIR spectroscopy, and TEM results suggest that the calcium phosphate deposited on the rutile TiO2 surfaces consist of carbonated calcium-deficient hydroxyapatite instead of octacalcium phosphate.

  10. Novel composites materials from functionalized polymers and silver coated titanium oxide capable for calcium phosphate induction, control of orthopedic biofilm infections: an "in vitro" study.

    Science.gov (United States)

    Tyllianakis, M; Dalas, E; Christofidou, M; Kallitsis, J K; Chrissanthopoulos, A; Koutsoukos, P G; Bartzavali, C; Gourdoupi, N; Papadimitriou, K; Oikonomou, E K; Yannopoulos, S N; Sevastos, D

    2010-07-01

    Three copolymers containing the functional groups P=O, S=O and C=O were prepared, and upon the introduction in calcium phosphate aqueous solutions at physiological conditions, "in vitro" were induced the precipitation of calcium phosphate crystals. The investigation of the crystal growth process was done at constant supersaturation. It is suggested that the negative end of the above functional groups acts as the active site for nucleation of the inorganic phase. In order to obtain the copolymer further antimicrobial activity, titania (TiO(2)) nanocrystals were incorporated in the polymer matrix after silver coverage by UV radiation. The antimicrobial resistance of the composite material (copolymer-titania/Ag) was tested against Staphylococcus epidermidis (SEM), Staphylococcus aureus (SAM), Candida parapsilosis (CAM) and Pseudomonas aeruginosa (PAM), microorganisms, using cut parts of "pi-plate" that covered with the above mentioned composite. The antimicrobial effect increased as the size of the nanocrystals TiO(2)/Ag decreased, the maximum achieved with the third polymer that contained also quartenary ammonium groups.

  11. 微弧氧化/电化学沉积钙磷涂层纯钛种植体的骨内植入*★%Endosseous implantation of calcium phosphate coated titanium implant prepared via micro-arc oxidation/electrochemical deposition

    Institute of Scientific and Technical Information of China (English)

    马盈; 孟祥才; 王静; 李德超

    2013-01-01

      背景:近年来已有对微弧氧化/电化学沉积技术制备涂层在材料性能方面的相关报道,但对这种材料植入体内的性能研究较少见。目的:观察纯钛种植体经微弧氧化/电化学沉积处理后的骨结合和新骨形成情况。方法:通过微弧氧化/电化学沉积方法在纯钛上制备含钙磷元素的涂层,然后将该种植体和纯钛种植体分别植入羊两侧胫骨种植窝内,于动物处死前15,5 d分别进行注射四环素进行四环素标记。术后4,12周分别进行X射线、扫描电镜及激光共聚焦观察。结果与结论:两侧X射线表现相似,种植体周围均无明显阴影,骨小梁排列和骨质密度与宿主骨基本一致。术后4周时,在电镜下可观察到两组种植体和骨组织之间均有间隙,部分见骨性结合;术后12周时,微弧氧化/电化学沉积种植体组可形成新骨,并且新骨与种植体和原来骨组织结合紧密,涂层与钛基体没有明显间隙,纯钛种植体组也可见新骨生成,但可看到明显裂隙。激光共聚焦观察显示,微弧氧化/电化学沉积种植体组双标记带间距离及骨矿化沉积率均高于纯钛种植体组(P <0.05)。表明微弧氧化/电化学沉积处理可增强纯钛种植体的骨结合能力及新骨形成。%  BACKGROUND: There are studies concerning material properties of coating prepared by micro-arc oxidation and electrochemical deposition, but there are few studies addressing properties of this kind of material implanted in the body. OBJECTIVE: To observe the synostosis and new bone formation of the pure titanium implant prepared by micro-arc oxidation/electrochemical deposition. METHODS: This research produces calcium and phosphate coatings on pure titanium though micro-arc oxidation/Electrochemical deposition technology, and the sheep were implanted with micro arc-oxidation/electrochemical deposition implant and pure titanium implant

  12. Comparative evaluation of microhardness of dentin treated with 4% titanium tetrafluoride and 1.23% acidic phosphate fluoride gel before and after exposure to acidic pH: An ex vivo study

    Science.gov (United States)

    Kandanuru, Vivek; Madhusudhana, Koppolu; Ramachandruni, Vamsi Krishna; Vitta, Harish Madhav; Babu, Lenin

    2016-01-01

    Aim: The aim of this study was to comparatively evaluate the effect of 4% titanium tetrafluoride (TiF4) and 1.23% acidic phosphate fluoride (APF) gel on the microhardness of human coronal dentin. Materials and Methods: Thirty noncarious extracted premolars were collected and sectioned buccolingually with the help of diamond disk. Exposing the sectioned surface, teeth were embedded in self-cure acrylic. Exposed coronal dentin was polished with abrasive papers starting with 220–5000 grit. Microhardness was evaluated by Vickers microhardness evaluator, at four different stages as follows - stage 1: Baseline values, Stage 2: Exposure of specimens to acidic environment at a pH 1 for 5 min, Stage 3: Application of 1.23% APF gel and 4% TiF4 (after dividing the specimens into two groups, i.e., Group A and B, respectively), and Stage 4: Followed by exposure of fluoridated specimens to acidic protocol as mentioned above. Results: Paired t-test was used to compare the readings between Groups A and B. Group B has shown greater resistance to decrease in microhardness of coronal dentin (P < 0.05) on exposure to acidic protocol. Conclusion: Due to acidic pH (1.5) of 4% TiF4, amount of increase in microhardness of dentin is <1.23% APF gel. 4% TiF4 was more effective in resisting demineralization than 1.23% APF gel. PMID:27994319

  13. Electrowinning molten titanium from titanium dioxide

    CSIR Research Space (South Africa)

    Van Vuuren, DS

    2005-10-01

    Full Text Available ; the high affinity of titanium for carbon, oxygen, and nitrogen; and physical and chemical properties of the different titanium oxide species when reducing titanium from Ti4+ to metallic titanium....

  14. A deposit model for magmatic iron-titanium-oxide deposits related to Proterozoic massif anorthosite plutonic suites: Chapter K in Mineral Deposit Models for Resource Assessment

    Science.gov (United States)

    Woodruff, Laurel G.; Nicholson, Suzanne W.; Fey, David L.

    2013-01-01

    This descriptive model for magmatic iron-titanium-oxide (Fe-Ti-oxide) deposits hosted by Proterozoic age massif-type anorthosite and related rock types presents their geological, mineralogical, geochemical, and geoenvironmental attributes. Although these Proterozoic rocks are found worldwide, the majority of known deposits are found within exposed rocks of the Grenville Province, stretching from southwestern United States through eastern Canada; its extension into Norway is termed the Rogaland Anorthosite Province. This type of Fe-Ti-oxide deposit dominated by ilmenite rarely contains more than 300 million tons of ore, with between 10- to 45-percent titanium dioxide (TiO2), 32- to 45-percent iron oxide (FeO), and less than 0.2-percent vanadium (V).

  15. Effect of Silanization on Titanium Surfaces by SAM on Biomimetic Mineralization Properties and Osteoblast Proliferation%钛表面自组装硅烷化对仿生矿化性能和细胞增殖的影响

    Institute of Scientific and Technical Information of China (English)

    张林; 谭帼馨; 宁成云; 刘绪建; 廖景文

    2012-01-01

    The pure titanium plates were modified by SAM using the organic solution with 3-aminopropyltriethoxysilane as the chief component and subsequently exposed to simulated body fluid for biomimetic mineralization. The surface morphologies and structures were characterized by attenuated total refraction-Fourier transform infrared spectroscopy (ATR-FTIR), scanning electronic microscopy (SEM) and X-ray diffraction (XRD); Human sweat gland cells (HMSCs) were planted on the surfaces of samples before and after modification, and then the adhesion and proliferation of HMSCs on the surfaces of titanium and its action before and after modification were investigated by MTT colorimetry and SEM. The results show that HCA coating is synthesized by biomimetic method and the ratio of Ca/P is 1.3. Compared with the pure titanium samples, the adhered HMSCs on the surfaces of titanium after modification by SAM are more, and the proliferation effect is obvious.%通过自组装技术以3-氨丙基三乙氧基硅烷为主要成分的有机溶液对纯钛进行表面改性处理,进一步将改性处理后的样品浸泡在模拟体液中仿生矿化处理,利用全反射红外光谱、扫描电镜和X射线衍射研究矿化处理前后样品的表面形貌与结构特征 ;将人骨髓间充质干细胞(HMSCs)种植于改性处理前后样品表面,利用四甲基偶氮唑盐微量酶反应比色法(MTT法)和扫描电镜观察细胞在改性前后样品表面的黏附、生长和增殖行为.结果表明,仿生矿化处理后,样品表面有类骨磷灰石生成,其钙/磷比为1.3 ;与纯钛相比,自组装硅烷化处理样品表面HMSCs的黏附率高,增殖效果明显.

  16. Prevention of bone mineral changes induced by bed rest: Modification by static compression simulating weight bearing, combined supplementation of oral calcium and phosphate, calcitonin injections, oscillating compression, the oral diophosphonatedisodium etidronate, and lower body negative pressure

    Science.gov (United States)

    Schneider, V. S.; Hulley, S. B.; Donaldson, C. L.; Vogel, J. M.; Rosen, S. N.; Hantman, D. A.; Lockwood, D. R.; Seid, D.; Hyatt, K. H.; Jacobson, L. B.

    1974-01-01

    The phenomenon of calcium loss during bed rest was found to be analogous to the loss of bone material which occurs in the hypogravic environment of space flight. Ways of preventing this occurrence are investigated. A group of healthy adult males underwent 24-30 weeks of continuous bed rest. Some of them were given an exercise program designed to resemble normal ambulatory activity; another subgroup was fed supplemental potassium phosphate. The results from a 12-week period of treatment were compared with those untreated bed rest periods. The potassium phosphate supplements prevented the hypercalciuria of bed rest, but fecal calcium tended to increase. The exercise program did not diminish the negative calcium balance. Neither treatment affected the heavy loss of mineral from the calcaneus. Several additional studies are developed to examine the problem further.

  17. Osteoclastic resorption of biomimetic calcium phosphate coatings in vitro.

    NARCIS (Netherlands)

    Leeuwenburgh, S.C.G.; Layrolle, P.; Barrere, F.; Bruijn, J.G.M. de; Schoonman, J.; Blitterswijk, C.A. van; Groot, K. de

    2001-01-01

    A new biomimetic method for coating metal implants enables the fast formation of dense and homogeneous calcium phosphate coatings. Titanium alloy (Ti6Al4V) disks were coated with a thin, carbonated, amorphous calcium phosphate (ACP) by immersion in a saturated solution of calcium, phosphate, magnesi

  18. Aggregate and Mineral Resources, PhosphateDeposits1988-This data set represents phosphate deposit areas in Utah., Published in 2001, Smaller than 1:100000 scale, State of Utah Automated Geographic Reference Center.

    Data.gov (United States)

    NSGIC GIS Inventory (aka Ramona) — This Aggregate and Mineral Resources dataset, published at Smaller than 1:100000 scale, was produced all or in part from Hardcopy Maps information as of 2001. It is...

  19. Increased chondrocyte adhesion on nanotubular anodized titanium.

    Science.gov (United States)

    Burns, Kevin; Yao, Chang; Webster, Thomas J

    2009-03-01

    Previous studies have demonstrated increased osteoblast (bone-forming cells) functions (including adhesion, synthesis of intracellular collagen, alkaline phosphatase activity, and deposition of calcium-containing minerals) on titanium anodized to possess nanometer features compared with their unanodized counterparts. Such titanium materials were anodized to possess novel nanotubes also capable of drug delivery. Since titanium has not only experienced wide spread commercial use in orthopedic but also in cartilage applications, the objective of the present in vitro study was for the first time to investigate chondrocyte (cartilage synthesizing cells) functions on titanium anodized to possess nanotubes. For this purpose, titanium was anodized in dilute hydrofluoric acid at 20 V for 20 min. Results showed increased chondrocyte adhesion on anodized titanium with nanotube structures compared with unanodized titanium. Importantly, the present study also provided evidence why. Since material characterization studies revealed significantly greater nanometer roughness and similar chemistry as well as crystallinity between nanotubular anodized and unanodized titanium, the results of the present study highlight the importance of the nanometer roughness provided by anodized nanotubes on titanium for enhancing chondrocyte adhesion. In this manner, the results of the present in vitro study indicated that anodization might be a promising quick and inexpensive method to modify the surface of titanium-based implants to induce better chondrocyte adhesion for cartilage applications.

  20. Transmission electron microscopy (TEM) study of minerals in coal

    Energy Technology Data Exchange (ETDEWEB)

    Hsieh, Kuang-Chien

    1982-01-01

    Minerals in eight coals from different mines were characterized in the micron-size range by using analytical transmission electron microscopy. Specimens were thinned by ion-milling wafers cut from these coals; a cold stage cooled by liquid nitrogen was used to reduce thermal degradation of the minerals by the ion-beam. Different mineral compounds were observed in different coals. The major minerals are clays, sulfides, oxides, carbonates and some minor-element-bearing phosphates. Clays (kaolinite, illite and others) have been most commonly found as either flat sheets or round globules. Iron sulfide was mostly found in the No. 5 and No. 6 coals from Illinois, distributed as massive polycrystals, as clusters of single crystals (framboids) or as isolated single crystals with size range down to some 0.25 microns. Other sulfides and some oxides were found in other coals with particle size as small as some 200 angstroms. Quartz, titanium oxides and many other carbonates and phosphate compounds were also characterized. Brief TEM work in the organic mass of coal was also introduced to study the nature of the coal macerals.

  1. [CKD-MBD (Chronic Kidney Disease-Mineral and Bone Disorder). Lanthanum carbonate and new phosphate binders in patients with chronic kidney disease].

    Science.gov (United States)

    Negi, Shigeo; Shigematsu, Takashi

    2010-07-01

    Hyperphosphatemia is a serious complication which has been linked with an increased risk of cardiovascular mortality in patients with chronic kidney disease. Lanthanum carbonate is a novel non-calcium, non-aluminum phosphate-binding agent, and has approved for clinical use in patients on hemodialysis in Japan on March in 2009. Compared to calcium carbonate and sevelamer hydrochloride, lanthanum carbonate is a powerful phosphate binder. There is no evidence of bone toxicity and neurotoxicity of lanthanum carbonate previously reported for aluminium hydroxide. However, further studies are needed to address the longer term toxic effect on bone and other organs.

  2. Differentiation of osteoblasts on pectin-coated titanium

    NARCIS (Netherlands)

    Kokkonen, H.; Cassinelli, C.; Verhoef, R.; Morra, M.; Schols, H.A.; Tuukkanen, J.

    2008-01-01

    The gold standard for implant metals is titanium, and coatings such as collagen-I, RGD-peptide, chondroitin sulfate, and calcium phosphate have been used to modify its biocompatibility. We investigated how titanium coated with pectins, adaptable bioactive plant polysaccharides with anti-inflammatory

  3. Chemistry, Raman and infrared spectroscopic characterization of the phosphate mineral reddingite: (MnFe)3(PO4)2(H2O,OH)3, a mineral found in lithium-bearing pegmatite

    Science.gov (United States)

    Frost, Ray L.; Xi, Yunfei; Scholz, Ricardo; Belotti, Fernanda M.; Lagoeiro, Leonardo E.

    2012-11-01

    Detailed investigation of an intermediate member of the reddingite-phosphoferrite series, using infrared and Raman spectroscopy, scanning electron microcopy and electron microprobe analysis, has been carried out on a homogeneous sample from a lithium-bearing pegmatite named Cigana mine, near Conselheiro Pena, Minas Gerais, Brazil. The determined formula is ({{Mn}}_{1.60} {{Fe}}_{1.21} {{Ca}}_{0.01} {{Mg}}_{0.01} )_{sum 2.83} ({{PO}}4 )_{2.12} \\cdot ({{H}}2 {{O}}_{2.85} {{F}}_{0.01} )_{sum 2.86} , indicating predominance in the reddingite member. Raman spectroscopy coupled with infrared spectroscopy supports the concept of phosphate, hydrogen phosphate and dihydrogen phosphate units in the structure of reddingite-phosphoferrite. Infrared and Raman bands attributed to water and hydroxyl stretching modes are identified. Vibrational spectroscopy adds useful information to the molecular structure of reddingite-phosphoferrite.

  4. Integrated mined-area reclamation and land use planning. Volume 3B. A case study of surface mining and reclamation planning: international minerals and chemical corporation, phosphate operations, Polk County, Florida. [Land reclamation and use planning for phosphate operations in Polk County, Florida

    Energy Technology Data Exchange (ETDEWEB)

    LaFevers, J R; Brown, L A; Fountain, R C

    1977-02-01

    The reports in this series are designed primarily to familiarize professional land use and resource planners with the range of possibilities and effective procedures for achieving integrated mining, reclamation, and land use planning. These reports are based on a research program which included an extensive literature review, the compilation and analysis of case study data, and close coordination and interaction with related government programs. In Volume 3, A Guide to Mined Area Reclamation Technology for Reclamation and Land Use Planners, the method used to reclaim land in each of several mineral industries are discussed in relation to the physical and cultural constraints that must be considered in planning a reclamation program. Much of the information for this document was obtained from case studies conducted in several mining districts. Volume 3B presents data from a case study of surface mining and reclamation planning, International Minerals and Chemical Corporation, Phosphate Operations, Polk County, Florida.

  5. Interfacial oxidations of pure titanium and titanium alloys with investments.

    Science.gov (United States)

    Ban, S; Watanabe, T; Mizutani, N; Fukui, H; Hasegawa, J; Nakamura, H

    2000-12-01

    External oxides of a commercially pure titanium (cpTi), Ti6Al4V alloy, and an experimental beta-type titanium alloy (Ti 53.4 wt%, Nb 29 wt%, Ta 13 wt%, and Zr 4.6 wt%) were characterized after heating to 600, 900, 1150, and 1400 degrees C in contact with three types of investments (alumina cement, magnesia cement, and phosphate-bonded) in air. XRD studies demonstrated that MgO, Li2TiO3 and/or Li2Ti3O7 were formed through reactions with the metal and the constituents in the magnesia cement-investment after heating to 900, 1150, and 1400 degrees C. Except for these conditions, TiO2 (rutile) was only formed on cpTi. For titanium alloys, the other components apart from Ti also formed simple and complex oxides such as Al2O3 and Al2TiO5 on Ti6Al4V, and Zr0.25Ti0.75Nb2O7 on the beta-type titanium alloy. However, no oxides containing V or Ta were formed. These results suggest that the constituents of titanium alloys reacted with the investment oxides and atmospheric oxygen to form external oxides due to the free energy of oxide formation and the concentration of each element on the metal surface.

  6. Titanium Alloys

    Directory of Open Access Journals (Sweden)

    Mark T. Whittaker

    2015-08-01

    Full Text Available Although originally discovered in the 18th century [1], the titanium industry did not experience any significant advancement until the middle of the 20th century through the development of the gas turbine engine [2]. Since then, the aerospace sector has dominated worldwide titanium use with applications in both engines and airframe structures [3]. The highly desirable combination of properties, which include excellent corrosion resistance, favourable strength to weight ratios, and an impressive resistance to fatigue, has led to an extensive range of applications [4], with only high extraction and processing costs still restricting further implementation. [...

  7. Influence of ceramic disk material, surface hemispheres, and SBF volume on in vitro mineralization.

    Science.gov (United States)

    Urquia Edreira, Eva R; Wolke, Joop G C; Jansen, John A; van den Beucken, Jeroen J J P

    2015-08-01

    Calcium phosphate ceramics are the main mineral constituents of bone and teeth and have therefore been extensively investigated for bone regenerative applications. In the current study, the effect of disk material, surface geometry, and SBF volume on mineralization capacity was investigated. Hemispherical concavities were created on the surfaces of disks made of different materials (i.e., hydroxyapatite (HA), β-tricalcium phosphate (β-TCP), biphasic calcium phosphate (BCP) and titanium (Ti)) which were sintered at 1200 °C. Mineralization of CaP was assessed on disk surfaces after immersion of the samples in different volumes of simulated body fluid (SBF) up to 14 days by means of calcium assay and scanning electron microscopy (SEM). This study showed that different SBF volumes have different effects on mineralization, with an optimum material/liquid ratio of 5 mL of SBF per cm(2) . Additionally, at this volume, apparent differences based on disk material became obvious. Evidently, surface hemispherical concavities acted as initiator areas for nucleation and crystal growth.

  8. Sodium Phosphate

    Science.gov (United States)

    Sodium phosphate is used in adults 18 years of age or older to empty the colon (large intestine, bowel) ... view of the walls of the colon. Sodium phosphate is in a class of medications called saline ...

  9. Phosphate salts

    Science.gov (United States)

    ... levels that are too high, and for preventing kidney stones. They are also taken for treating osteomalacia (often ... But intravenous phosphate salts should not be used. Kidney stones (nephrolithiasis). Taking potassium phosphate by mouth might help ...

  10. Dedifferentiated fat cells differentiate into osteoblasts in titanium fiber mesh.

    Science.gov (United States)

    Kishimoto, Naotaka; Momota, Yoshihiro; Hashimoto, Yoshiya; Ando, Kayoko; Omasa, Takeshi; Kotani, Junichiro

    2013-01-01

    Mature adipocyte-derived dedifferentiated fat (DFAT) cells rapidly differentiate into osteoblasts under three-dimensional culture conditions. However, it has not been demonstrated that DFAT cells can differentiate into osteoblasts in a rigid scaffold consisting of titanium fiber mesh (TFM). We examined the proliferation and osteogenic differentiation ability of DFAT cells using TFM as a scaffold. DFAT cells derived from rabbit subcutaneous fat were seeded into TFM and cultured in osteogenic medium containing dexamethasone, L-ascorbic acid 2-phosphate and β-glycerophosphate for 14 days. In scanning electron microscopy (SEM) analysis, well-spread cells covered the titanium fibers on day 3, and appeared to increase in number from day 3 to 7. Numerous globular accretions were found and almost completely covered the fibers on day 14. Cell proliferation, as measured by DNA content in the TFM, was significantly higher on day 7 compared with that of day 1. Osteocalcin and calcium content in the TFM were significantly higher on day 14 compared to those of days 1, 3, and 7, indicating DFAT cells differentiated into osteoblasts. We theorize that globular accretions observed in SEM analysis may be calcified matrix resulting from osteocalcin secreted by osteoblasts binding calcium contained in fetal bovine serum. In this study, we demonstrated that DFAT cells differentiate into osteoblasts and deposit mineralized matrices in TFM. Therefore, the combination of DFAT cells and TFM may be an attractive option for bone tissue engineering.

  11. Response of serum minerals (calcium, phosphate, and magnesium) and endocrine glands (calcitonin cells and parathyroid gland) of Wistar rat after chlorpyrifos administration.

    Science.gov (United States)

    Tripathi, Sarojni; Suzuki, Nobuo; Srivastav, Ajai Kumar

    2013-07-01

    Wistar rats (male) were daily administered chlorpyrifos at a dose of 5 mg/kg b wt. and 10 mg/kg b wt. and sacrificed on 1st, 2nd, 4th, 6th, and 8th week. In chlorpyrifos exposed rats hypocalcemia, hypophosphatemia and hypomagnesemia were recorded. At later intervals an increased levels of serum calcium and phosphate were observed. The parathyroid glands and calcitonin cells exhibited increased activity which is evident by increased nuclear volume of these cells. Copyright © 2013 Wiley Periodicals, Inc.

  12. Phosphate control in dialysis.

    Science.gov (United States)

    Cupisti, Adamasco; Gallieni, Maurizio; Rizzo, Maria Antonietta; Caria, Stefania; Meola, Mario; Bolasco, Piergiorgio

    2013-10-04

    Prevention and correction of hyperphosphatemia is a major goal of chronic kidney disease-mineral and bone disorder (CKD-MBD) management, achievable through avoidance of a positive phosphate balance. To this aim, optimal dialysis removal, careful use of phosphate binders, and dietary phosphate control are needed to optimize the control of phosphate balance in well-nourished patients on a standard three-times-a-week hemodialysis schedule. Using a mixed diffusive-convective hemodialysis tecniques, and increasing the number and/or the duration of dialysis tecniques are all measures able to enhance phosphorus (P) mass removal through dialysis. However, dialytic removal does not equal the high P intake linked to the high dietary protein requirement of dialysis patients; hence, the use of intestinal P binders is mandatory to reduce P net intestinal absorption. Unfortunately, even a large dose of P binders is able to bind approximately 200-300 mg of P on a daily basis, so it is evident that their efficacy is limited in the case of an uncontrolled dietary P load. Hence, limitation of dietary P intake is needed to reach the goal of neutral phosphate balance in dialysis, coupled to an adequate protein intake. To this aim, patients should be informed and educated to avoid foods that are naturally rich in phosphate and also processed food with P-containing preservatives. In addition, patients should preferentially choose food with a low P-to-protein ratio. For example, patients could choose egg white or protein from a vegetable source. Finally, boiling should be the preferred cooking procedure, because it induces food demineralization, including phosphate loss. The integrated approach outlined in this article should be actively adapted as a therapeutic alliance by clinicians, dieticians, and patients for an effective control of phosphate balance in dialysis patients.

  13. Corrosion of titanium in supercritical water oxidation environments

    Institute of Scientific and Technical Information of China (English)

    卢建树; 毛志远; 张九渊; 马淳安; 毛信表; 李肖华

    2002-01-01

    Supercritical water oxidation (SCWO) can effectively destroy many kinds of civilian and military wastes. The high temperature and high pressure SCWO operation conditions generate very corrosive environment that many engineering materials fail to withstand. Preliminary test shows that titanium may be a promising material in most of SCWO conditions. Commercially pure titanium is tested in four kinds of SCWO environments. Phenol, sodium dodecyl-benzosulfonate, n-amine phenol, and chlorpyrifos were chosen as typical target pollutants. The results show that titanium is only superficially attacked in the first three SCWO environments while in chlorpyrifos SCWO medium titanium is corroded. The corrosion is temperature dependent, with heavier corrosion occurring at near critical temperature. X-ray diffraction analysis shows that the corrosion products consist of titanium oxy- phosphates and titanium oxide, in which Ti5O4(PO4)4 is the main phase.

  14. Aluminium phosphate sulphate minerals (APS) associated with proterozoic unconformity-type uranium deposits: crystal-chemical characterisation and petrogenetic significance; Les sulfates phosphates d'aluminium hydrates (APS) dans l'environnement des gisements d'uranium associes a une discordance proterozoique: caracterisation cristallochimique et signification petrogenetique

    Energy Technology Data Exchange (ETDEWEB)

    Gaboreau, St

    2005-07-01

    Aluminium phosphate sulfate minerals (APS) are particularly widespread and spatially associated with hydrothermal clay alteration in both the East Alligator River Uranium Field (Northern Territory, Australia) and the Athabasca basin (Saskatchewan, Canada), in the environment of proterozoic unconformity-related uranium deposits (URUD). The purpose of this study is both: 1) to characterize the nature and the origin of the APS minerals on both sides of the middle proterozoic unconformity between the overlying sandstones and the underlying metamorphic basement rocks that host the uranium ore bodies, 2) to improve our knowledge on the suitability of these minerals to indicate the paleo-conditions (redox, pH) at which the alteration processes relative to the uranium deposition operated. The APS minerals result from the interaction of oxidising and relatively acidic fluids with aluminous host rocks enriched in monazite. Several APS-bearing clay assemblages and APS crystal-chemistry have also been distinguished as a function of the distance from the uranium ore bodies or from the structural discontinuities which drained the hydrothermal solutions during the mineralisation event. One of the main results of this study is that the index mineral assemblages, used in the recent literature to describe the alteration zones around the uranium ore bodies, can be theoretically predicted by a set of thermodynamic calculations which simulate different steps of fluid-rock interaction processes related to a downward penetrating of hyper-saline, oxidizing and acidic diagenetic fluids through the lower sandstone units of the basins and then into the metamorphic basement rocks. The above considerations and the fact that APS with different crystal-chemical compositions crystallized in a range of fO{sub 2} and pH at which uranium can either be transported in solution or precipitated as uraninite in the host-rocks make these minerals not only good markers of the degree of alteration of the

  15. Comparison of calcium carbonate and aluminium hydroxide as phosphate binders on biochemical bone markers, PTH(1-84), and bone mineral content in dialysis patients

    DEFF Research Database (Denmark)

    Jespersen, B; Jensen, J D; Nielsen, H K;

    1991-01-01

    Bone mineral content, estimated by single-photon absorptiometry of the forearm, serum values of intact parathyroid hormone (PTH(1-84], osteocalcin, alkaline phosphatase, 1,25-dihydroxycholecalciferol (1,25(OH)2D3), and aluminium were determined during treatment with calcium carbonate (CaCO3...... 0.05), osteocalcin decreased (89% versus 117%, P less than 0.01), alkaline phosphatase decreased (92% versus 116%, P less than 0.05), and aluminium decreased (56% versus 189%, P less than 0.05). 1,25(OH)2D3 remained unchanged in both periods. No increase in soft-tissue calcification was demonstrated......) or aluminium hydroxide (Al(OH)3) in 11 dialysis patients participating in a randomised cross-over study. Each treatment period lasted 6 months. Serum phosphorus was maintained in the range 1.5-2.0 mmol/l. During Al(OH)3 treatment bone mineral content (BMC) decreased by 11% per half-year (mean), but only by 3...

  16. Electrosprayed calcium phosphate coatings for biomedical purposes

    NARCIS (Netherlands)

    Leeuwenburgh, Sander Cornelis Gerardus

    2006-01-01

    In this thesis, the suitability of the Electrostatic Spray Deposition (ESD) technique was studied for biomedical purposes, i.e., deposition of calcium phosphate (CaP) coatings onto titanium substrates. Using ESD, which is a simple and cheap deposition method for inorganic and organic coatings, it wa

  17. Titanium in 1980

    Science.gov (United States)

    Minkler, Ward W.

    1981-04-01

    Much attention is being focused on the availability and use of non-fuel minerals in the United States. Because of the rapid increase in demand since 1978, titanium has been one of the much-publicized metals in this group. Sponge producers are now expanding sponge manufacturing plants to meet this greater demand, and it now appears that there could be a surplus of sponge in 1981. A delay in airplane purchases caused by severe operating losses of the airlines could have a significant effect on mill product shipments in 1981. However, there is no reason to believe that titanium has reached maturity as a structural aerospace or industrial metal. While it is unreasonable to anticipate that demand will continue to grow at the same rate experienced between 1978 and 1980, new greenfield capacity will nevertheless be required in the early 1980s. Two basic issues must be resolved before such ventures become reality: 1) choice of process; and 2) method for financing, either public or private. Both will be the subject of study and debate in 1981.

  18. Method for preparing hydrous titanium oxide spherules and other gel forms thereof

    Science.gov (United States)

    Collins, J.L.

    1998-10-13

    The present invention are methods for preparing hydrous titanium oxide spherules, hydrous titanium oxide gels such as gel slabs, films, capillary and electrophoresis gels, titanium monohydrogen phosphate spherules, hydrous titanium oxide spherules having suspendible particles homogeneously embedded within to form a composite sorbent, titanium monohydrogen phosphate spherules having suspendible particles of at least one different sorbent homogeneously embedded within to form a composite sorbent having a desired crystallinity, titanium oxide spherules in the form of anatase, brookite or rutile, titanium oxide spherules having suspendible particles homogeneously embedded within to form a composite, hydrous titanium oxide fiber materials, titanium oxide fiber materials, hydrous titanium oxide fiber materials having suspendible particles homogeneously embedded within to form a composite, titanium oxide fiber materials having suspendible particles homogeneously embedded within to form a composite and spherules of barium titanate. These variations of hydrous titanium oxide spherules and gel forms prepared by the gel-sphere, internal gelation process offer more useful forms of inorganic ion exchangers, catalysts, getters and ceramics. 6 figs.

  19. Uso de Fosfato Bicálcico Granulado Sobre o Desempenho e Mineralização Óssea de Frangos de Corte Effect of Granulated Dicalcium Phosphate on the Performance and Bone Mineralization in Broilers

    Directory of Open Access Journals (Sweden)

    OM Junqueira

    2001-01-01

    Full Text Available O objetivo do experimento foi avaliar os efeitos do tamanho da partícula do fosfato bicálcico (fina ou granulada e dos níveis de fósforo total sobre o desempenho de frangos de corte e sobre os teores de cálcio, fósforo e magnésio dos ossos. O delineamento experimental utilizado foi o inteiramente casualizado em esquema fatorial 3x2 com 3 níveis de fósforo total (0,5%; 0,6% e 0,7% e duas granulometrias de fosfato bicálcico (fina e granulada. Foram utilizados 300 pintos de corte com um dia de idade, machos, da linhagem Cobb, alojados em baterias metálicas em 6 tratamentos com 5 repetições de 10 aves, totalizando 30 gaiolas dispostas em 6 baterias de 5 andares cada. Os resultados demonstraram que o uso do fosfato granulado resultou em melhor desempenho dos animais. Aves alimentadas com o nível de 0,5% de fósforo total apresentaram o pior desempenho, sendo que o nível de 0,6% proporcionou melhor desempenho das aves. As diferentes granulometrias do fosfato, não diferiram estatisticamente quanto a percentagem de matéria mineral, cálcio, fósforo e magnésio nos ossos.The objective of the experiment was to evaluate the effects of particle size of dicalcium phosphate (fine or granulated and of the levels of total phosphorus on the performance of broilers and levels of calcium, phosphorus and magnesium of the bones. Three hundred one-day chicks, males, Cobb strain, were used in an experimental design involving six treatments in a factorial arrangement 2x3 (2 particles size of dicalcium phosphate and 3 phosphorus levels of 0,5%, 0,6% e 0,7%. It was concluded that the addition of granulated dicalcium phosphate resulted in a better performance. The level of 0,5% total phosphorus depressed body weight gain, feed intake and feed conversion and level 0,6% showed better performance. Total bone ash and bone calcium were not affected by treatments, however, better bone phosphorus was found when the broilers received the diet with 0,7% total

  20. Engineering titanium surfaces for improving osteointegration

    Science.gov (United States)

    Lu, Xiong

    Titanium is one of the most important metallic biomedical materials in clinical applications. One of the key issues for successful application of titanium is the interaction at the interface between the titanium and the bone. The present study focuses on improving the surfaces of titanium to achieve better capability to bond with natural bone (i.e. better osteointegration). The objectives of this work include: (1) Developing microfabrication methods to produce micropatterns on titanium surfaces for promoting osteointegration; (2) Studying the calcium phosphate (Ca-P) formation on the chemical treated titanium surface and elucidating the mechanism of precipitation theoretically; and (3) Evaluating osteoconductivity of engineering titanium surfaces in vitro and in vivo. Through mask electrochemical micromachining (TMEMM), jet electrochemical micromachining (Jet-EMM) and the confined etchant layer technique (CELT) were attempted to produce micropatterns on titanium surfaces. TMEMM has a high etching rate and good reproducibility and was used to produce micro-hole arrays on Ti plates for in vivo testing. The driving force and nucleation rate of Ca-P precipitation in simulated body fluid (SBF) were analyzed based on the classical crystallization theory. SBF supersaturation with respect to HA, OCP and DCPD (dicalcium phosphate) was carefully calculated, considering all the association/dissociation reactions of related ion groups in SBF. The analysis indicates that the nucleation rate of OCP is substantially higher than that of HA, while HA is most thermodynamically stable in SBF. DCPD precipitation is thermodynamically impossible in normal SBF, unless calcium and phosphate ion concentrations of SBF increase. Osteoconduction of Ti6Al4V surfaces under various conditions, including micro-patterned, alkali-treated, micro-patterned plus alkali-treated, and surfaces without any treatment, was evaluated. TMEMM was used to fabricate micro-hole arrays on the titanium alloy

  1. Vibrational spectroscopic characterization of the phosphate mineral althausite Mg2(PO4)(OH,F,O)--implications for the molecular structure.

    Science.gov (United States)

    Frost, Ray L; López, Andrés; Xi, Yunfei; Scholz, Ricardo

    2014-01-01

    Natural single-crystal specimens of althausite from Brazil, with general formula Mg2(PO4)(OH,F,O) were investigated by Raman and infrared spectroscopy. The mineral occurs as a secondary product in granitic pegmatites. The Raman spectrum of althausite is characterized by bands at 1020, 1033 and 1044 cm(-1), assigned to ν1 symmetric stretching modes of the HOPO3(3-) and PO4(3-) units. Raman bands at around 1067, 1083 and 1138 cm(-1) are attributed to both the HOP and PO antisymmetric stretching vibrations. The set of Raman bands observed at 575, 589 and 606 cm(-1) are assigned to the ν4 out of plane bending modes of the PO4 and H2PO4 units. Raman bands at 439, 461, 475 and 503 cm(-1) are attributed to the ν2 PO4 and H2PO4 bending modes. Strong Raman bands observed at 312, 346 cm(-1) with shoulder bands at 361, 381 and 398 cm(-1) are assigned to MgO stretching vibrations. No bands which are attributable to water were found. Vibrational spectroscopy enables aspects of the molecular structure of althausite to be assessed. Copyright © 2013 Elsevier B.V. All rights reserved.

  2. 自固化磷酸钙人工骨植骨联合可塑形钛板内固定治疗 Sanders Ⅲ,Ⅳ型跟骨骨折%Autosetting Calcium Phosphate Cement Bone-Grafting and Internal Fixation with Shaping Titanium Plate for Treatment of SandersⅢ,ⅣCalcaneal Fractures

    Institute of Scientific and Technical Information of China (English)

    韩振学; 李志仙

    2014-01-01

    [ ABSTRACT] Objective To investigate the curative effect of Sanders Ⅲ,Ⅳ calcaneal fractures by autosetting calcium phosphate cement bone-grafting and internal fixation with shaping titanium plate.Methods Twenty-eight cases(28 feet) SandersⅢ,Ⅳcalcaneal frac-tures adopted open reduction with shaping titanium plate internal fixation combined with autosetting calcium phosphate cement bone-grafting, the shaping titanium plate were placed at the outward of calcaneus,reset evaluation of calcaneal fractures by measuring Bohler's Angle,Gis-sane's Angle in postoperation.Results All patients were followed up,postoperative skin necrosis in 2 cases and sural nerve injury in 1 case. After 6 months,Bohler's Angle in 20 foot≥35°,in 8 foot≥30°,Gissane Angle fully recovered to normal range and calcaneal varus deformity on axial were not seen.Fracture healing time was 2~3 months,according to Maryland foot scoring system,treatment effects of all patients were as follows:excellent in 15 feet,good in 5 feet,normal in 3 feet and poor in 2 feet,the total excellent and good rate was 83.7%,the excel-lent and good rate ofⅣtype was 56.2%.Conclusion The treatment of SandersⅢ,Ⅳcalcaneal fractures by autosetting calcium phosphate cement bone-grafting and internal fixation with shaping titanium plate is simple and its curative effect is satisfied.%目的:探讨自固化磷酸钙人工骨植骨联合可塑形钛板内固定治疗Sanders Ⅲ,Ⅳ型跟骨骨折的疗效。方法对28例(28足) SandersⅢ,Ⅳ型跟骨骨折均采用切开复位可塑形钛板固定联合自固化磷酸钙人工骨治疗,跟骨外侧放置可塑形钛板,术后测量Bohler's 角、Gissane's角,评价跟骨骨折的复位情况。结果所有患者均得到随访,术后皮缘坏死2例,腓肠神经损伤1例。术后6个月Bohler's 角20足≥35°,8足≥30°,Gissane角全部恢复至正常范围,轴位片上未见跟骨内翻畸形。骨折愈合时间2~3个月,

  3. Rapid prototyped porous nickel-titanium scaffolds as bone substitutes.

    Science.gov (United States)

    Hoffmann, Waldemar; Bormann, Therese; Rossi, Antonella; Müller, Bert; Schumacher, Ralf; Martin, Ivan; de Wild, Michael; Wendt, David

    2014-01-01

    While calcium phosphate-based ceramics are currently the most widely used materials in bone repair, they generally lack tensile strength for initial load bearing. Bulk titanium is the gold standard of metallic implant materials, but does not match the mechanical properties of the surrounding bone, potentially leading to problems of fixation and bone resorption. As an alternative, nickel-titanium alloys possess a unique combination of mechanical properties including a relatively low elastic modulus, pseudoelasticity, and high damping capacity, matching the properties of bone better than any other metallic material. With the ultimate goal of fabricating porous implants for spinal, orthopedic and dental applications, nickel-titanium substrates were fabricated by means of selective laser melting. The response of human mesenchymal stromal cells to the nickel-titanium substrates was compared to mesenchymal stromal cells cultured on clinically used titanium. Selective laser melted titanium as well as surface-treated nickel-titanium and titanium served as controls. Mesenchymal stromal cells had similar proliferation rates when cultured on selective laser melted nickel-titanium, clinically used titanium, or controls. Osteogenic differentiation was similar for mesenchymal stromal cells cultured on the selected materials, as indicated by similar gene expression levels of bone sialoprotein and osteocalcin. Mesenchymal stromal cells seeded and cultured on porous three-dimensional selective laser melted nickel-titanium scaffolds homogeneously colonized the scaffold, and following osteogenic induction, filled the scaffold's pore volume with extracellular matrix. The combination of bone-related mechanical properties of selective laser melted nickel-titanium with its cytocompatibility and support of osteogenic differentiation of mesenchymal stromal cells highlights its potential as a superior bone substitute as compared to clinically used titanium.

  4. Phosphate control in dialysis

    Directory of Open Access Journals (Sweden)

    Cupisti A

    2013-10-01

    Full Text Available Adamasco Cupisti,1 Maurizio Gallieni,2 Maria Antonietta Rizzo,2 Stefania Caria,3 Mario Meola,4 Piergiorgio Bolasco31Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy; 2Nephrology and Dialysis Unit, San Carlo Borromeo Hospital, Milan, Italy; 3Territorial Department of Nephrology and Dialysis, ASL Cagliari, Italy; 4Sant'Anna School of Advanced Studies, University of Pisa, Pisa, ItalyAbstract: Prevention and correction of hyperphosphatemia is a major goal of chronic kidney disease–mineral and bone disorder (CKD–MBD management, achievable through avoidance of a positive phosphate balance. To this aim, optimal dialysis removal, careful use of phosphate binders, and dietary phosphate control are needed to optimize the control of phosphate balance in well-nourished patients on a standard three-times-a-week hemodialysis schedule. Using a mixed diffusive–convective hemodialysis tecniques, and increasing the number and/or the duration of dialysis tecniques are all measures able to enhance phosphorus (P mass removal through dialysis. However, dialytic removal does not equal the high P intake linked to the high dietary protein requirement of dialysis patients; hence, the use of intestinal P binders is mandatory to reduce P net intestinal absorption. Unfortunately, even a large dose of P binders is able to bind approximately 200–300 mg of P on a daily basis, so it is evident that their efficacy is limited in the case of an uncontrolled dietary P load. Hence, limitation of dietary P intake is needed to reach the goal of neutral phosphate balance in dialysis, coupled to an adequate protein intake. To this aim, patients should be informed and educated to avoid foods that are naturally rich in phosphate and also processed food with P-containing preservatives. In addition, patients should preferentially choose food with a low P-to-protein ratio. For example, patients could choose egg white or protein from a vegetable source

  5. Vibrational spectroscopy of the phosphate mineral lazulite - (Mg, Fe)Al2(PO4)2·(OH)2 found in the Minas Gerais, Brazil

    Science.gov (United States)

    Frost, Ray L.; Xi, Yunfei; Beganovic, Martina; Belotti, Fernanda Maria; Scholz, Ricardo

    2013-04-01

    This research was done on lazulite samples from the Gentil mine, a lithium bearing pegmatite located in the municipality of Mendes Pimentel, Minas Gerais, Brazil. Chemical analysis was carried out by electron microprobe analysis and indicated a magnesium rich phase with partial substitution of iron. Traces of Ca and Mn, (which partially replaced Mg) were found. The calculated chemical formula of the studied sample is: (Mg0.88, Fe0.11)Al1.87(PO4)2.08(OH)2.02. The Raman spectrum of lazulite is dominated by an intense sharp band at 1060 cm-1 assigned to PO stretching vibrations of of tetrahedral [PO4] clusters presents into the HPO42- units. Two Raman bands at 1102 and 1137 cm-1 are attributed to both the HOP and PO antisymmetric stretching vibrations. The two infrared bands at 997 and 1007 cm-1 are attributed to the ν1PO43- symmetric stretching modes. The intense bands at 1035, 1054, 1081, 1118 and 1154 cm-1 are assigned to the ν3PO43- antisymmetric stretching modes from both the HOP and tetrahedral [PO4] clusters. A set of Raman bands at 605, 613, 633 and 648 cm-1 are assigned to the ν4 out of plane bending modes of the PO4, HPO4 and H2PO4 units. Raman bands observed at 414, 425, 460, and 479 cm-1 are attributed to the ν2 tetrahedral PO4 clusters, HPO4 and H2PO4 bending modes. The intense Raman band at 3402 and the infrared band at 3403 cm-1 are assigned to the stretching vibration of the OH units. A combination of Raman and infrared spectroscopy enabled aspects of the molecular structure of the mineral lazulite to be understood.

  6. Opportunities in the electrowinning of molten titanium from titanium dioxide

    CSIR Research Space (South Africa)

    Van Vuuren, DS

    2005-10-01

    Full Text Available ; the high affinity of titanium for carbon, oxygen, and nitrogen; and physical and chemical properties of the different titanium oxide species when reducing titanium from Ti4+ to metallic titanium....

  7. Electrochemical Characteristics of Titanium for Dental Implants in Case of the Electroless Surface Modification

    Directory of Open Access Journals (Sweden)

    Klimecka-Tatar D.

    2016-06-01

    Full Text Available In the paper the results of research under effect of electroless phosphate coating of titanium dental implants on potentiokinetic polarization characteristic obtained in artificial saliva were presented. On the basis of electrochemical studies it was concluded that the electroless process of phosphating beneficialy effect on corrosion characteristic of titanium determined in solution simulating the oral cavity. Furthermore, the proposed technique of chemical treatment of titanium surface is conducive to the homogeneous development of the surface, which is extremely important from the point of view of titanium implants biointegration. Phosphating treatment affect on the development of surface geometry, resulting in a slight increase in roughness parameters (Ra, Rz and Rmax. The temperature increase of electroless phosphating treatment promotes the rate of conversion layer formation, whereas the effect of temperature of the chemical treatment efficiency is secondary important at longer exposure times (e.g. 45 minutes.

  8. Titanium and titanium alloys fundamentals and applications

    CERN Document Server

    Peters, Manfred

    2003-01-01

    This handbook is an excellent reference for materials scientists and engineers needing to gain more knowledge about these engineering materials. Following introductory chapters on the fundamental materials properties of titanium, readers will find comprehensive descriptions of the development, processing and properties of modern titanium alloys. There then follows detailed discussion of the applications of titanium and its alloys in aerospace, medicine, energy and automotive technology.

  9. Phosphate solubilizing bacteria and their role in plant growth promotion.

    Science.gov (United States)

    Rodríguez, H; Fraga, R

    1999-10-01

    The use of phosphate solubilizing bacteria as inoculants simultaneously increases P uptake by the plant and crop yield. Strains from the genera Pseudomonas, Bacillus and Rhizobium are among the most powerful phosphate solubilizers. The principal mechanism for mineral phosphate solubilization is the production of organic acids, and acid phosphatases play a major role in the mineralization of organic phosphorous in soil. Several phosphatase-encoding genes have been cloned and characterized and a few genes involved in mineral phosphate solubilization have been isolated. Therefore, genetic manipulation of phosphate-solubilizing bacteria to improve their ability to improve plant growth may include cloning genes involved in both mineral and organic phosphate solubilization, followed by their expression in selected rhizobacterial strains. Chromosomal insertion of these genes under appropriate promoters is an interesting approach.

  10. Chinese titanium industry

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    <正>The effects of the financial crisis on the titanium industry are visible: investment plans for titanium smelting and processing have basically come to a halt in 2009, and projects under construction were also delayed. However, the

  11. Jörgkellerite, Na3Mn3+ 3(PO4)2(CO3)O2·5H2O, a new layered phosphate-carbonate mineral from the Oldoinyo Lengai volcano, Gregory rift, northern Tanzania

    Science.gov (United States)

    Zaitsev, Anatoly N.; Britvin, Sergey N.; Kearsley, Anton; Wenzel, Thomas; Kirk, Caroline

    2016-12-01

    Jörgkellerite, ideally Na3Mn3+ 3(PO4)2(CO3)O2·5H2O, is a new layered phosphate-carbonate from the Oldoinyo Lengai volcano in the Gregory Rift (northern Tanzania). The mineral occurs as spherulites, up to 200 μm in diameter, consisting of plates up to 10 μm in thickness in shortite-calcite and calcite carbonatites. Jörgkellerite is brown with a vitreous lustre and has a perfect micaceous cleavage on {001}, Mohs hardness is 3. The calculated density is 2.56 g/cm3. Jörgkellerite is uniaxial (-), ω = 1.700(2), ɛ = 1.625(2) (Na light, 589 nm) with distinct pleochroism: O = dark brown, E = light brown. The empirical formula of the mineral (average of 10 electron microprobe analyses) is (Na2.46K0.28Ca0.08Sr0.04Ba0.02)Σ2.88(Mn3+ 2.39Fe3+ 0.56)Σ2.95((PO4)1.95(SiO4)0.05))Σ2.00(CO3)(O1.84(OH)0.16)Σ2.00·5H2O. The oxidation state of Mn has been determined by XANES. Jörgkellerite is trigonal, space group P-3, a = 11.201(2) Å, c = 10.969(2) Å, V = 1191.9(7) Å3 and Z = 3. The five strongest powder-diffraction lines [d in Å, (I/I o), (hkl)] are: 10.970 (100) (001), 5.597 (15) (002), 4.993 (8) (111), 2.796 (14) (220) and 2.724 (20) (004). The crystal structure is built up of the layers composed of disordered edge-sharing [MnO6] octahedra. Each fourth Mn site in octahedral layer is vacant that results in appearance of ordered system of hexagonal "holes" occupied by (CO3) groups. The overall composition of the layer can be expressed as [Mn3O8(CO3)]. These manganese-carbonate layers are linked in the third dimension by (PO4) tetrahedra and Na-polyhedra. The origin of jörgkellerite is related to low-temperature oxidative alteration of gregoryite-nyerereite carbonatites.

  12. Cloning of an Erwinia herbicola gene necessary for gluconic acid production and enhanced mineral phosphate solubilization in Escherichia coli HB101: nucleotide sequence and probable involvement in biosynthesis of the coenzyme pyrroloquinoline quinone.

    Science.gov (United States)

    Liu, S T; Lee, L Y; Tai, C Y; Hung, C H; Chang, Y S; Wolfram, J H; Rogers, R; Goldstein, A H

    1992-09-01

    Escherichia coli is capable of synthesizing the apo-glucose dehydrogenase enzyme (GDH) but not the cofactor pyrroloquinoline quinone (PQQ), which is essential for formation of the holoenzyme. Therefore, in the absence of exogenous PQQ, E. coli does not produce gluconic acid. Evidence is presented to show that the expression of an Erwinia herbicola gene in E. coli HB101(pMCG898) resulted in the production of gluconic acid, which, in turn, implied PQQ biosynthesis. Transposon mutagenesis showed that the essential gene or locus was within a 1.8-kb region of a 4.5-kb insert of the plasmid pMCG898. This 1.8-kb region contained only one apparent open reading frame. In this paper, we present the nucleotide sequence of this open reading frame, a 1,134-bp DNA fragment coding for a protein with an M(r) of 42,160. The deduced sequence of this protein had a high degree of homology with that of gene III (M(r), 43,600) of a PQQ synthase gene complex from Acinetobacter calcoaceticus previously identified by Goosen et al. (J. Bacteriol. 171:447-455, 1989). In minicell analysis, pMCG898 encoded a protein with an M(r) of 41,000. These data indicate that E. coli HB101(pMCG898) produced the GDH-PQQ holoenzyme, which, in turn, catalyzed the oxidation of glucose to gluconic acid in the periplasmic space. As a result of the gluconic acid production, E. coli HB101(pMCG898) showed an enhanced mineral phosphate-solubilizing phenotype due to acid dissolution of the hydroxyapatite substrate.

  13. Sealing ability of mineral trioxide aggregate, calcium phosphate and polymethylmethacrylate bone cements on root ends prepared using an Erbium: Yttriumaluminium garnet laser and ultrasonics evaluated by confocal laser scanning microscopy.

    Science.gov (United States)

    Girish, C Sabari; Ponnappa, Kc; Girish, Tn; Ponappa, Mc

    2013-07-01

    Surgical endodontic therapy comprises of exposure of the involved root apex, resection of the apical end of the root, preparation of a class I cavity, and insertion of a root end filling material. Mineral trioxide aggregate (MTA) is now the gold standard among all root end filling materials. MTA is however difficult to handle, expensive and has a very slow setting reaction. (1) To compare the sealing ability of MTA, polymethylmethacrylate (PMMA) bone cement and CHITRA Calcium phosphate cement (CPC) when used as root end filling material using Rhodamine B dye evaluated under a confocal laser scanning microscope. (2) To compare the seal of root ends prepared using an ultrasonic retroprep tip and an Er: YAG laser using three different root end filling materials. Statistical analysis was performed using a one-way ANOVA and a two-way ANOVA, independent samples t-test and Scheffe's post hoc test using SPSS Version 16 for Windows. All the three materials, namely MTA, PMMA BONE CEMENT and CHITRA CPC, showed microleakage. Comparison of microleakage showed maximum peak value of 0.86 mm for MTA, 0.24 mm for PMMA bone cement and 1.37 mm for CHITRA CPC. The amount of dye penetration was found to be lesser in root ends prepared using Er: YAG laser when compared with ultrasonics, but the difference was found to be not statistically significant. PMMA bone cement is a better material as root end filling material to prevent apical microleakage. MTA still continues to be a gold standard root end filling material showing minimum microleakage. Er: YAG laser is a better alternative to ultrasonics for root end preparations.

  14. Titanium Carbide-Graphite Composites

    Science.gov (United States)

    1991-11-08

    titanium carbide , titanium carbide with free graphite, titanium carbide /vanadium carbide alloy with free graphite, and titanium carbide with...from melts. The test pins were drawn across hot pressed titanium carbide wear plates with 5 newtons of normal force. The lowest friction coefficient at...22 C was 0.12 obtained with pure titanium carbide . The lowest friction coefficient at 900 C was 0.19 obtained with titanium carbide with boron and

  15. Carbamazepine degradation by photolysis and titanium dioxide photocatalysis.

    Science.gov (United States)

    Im, Jong-Kwon; Son, Hyun-Seok; Kang, Young-Min; Zoh, Kyung-Duk

    2012-07-01

    We investigated the degradation of carbamazepine by photolysis/ultraviolet (UV)-C only and titanium dioxide photocatalysis. The degradation of carbamazepine by UV-only and titanium-dioxide-only (adsorption) reactions were inefficient, however, complete degradation of carbamazepine was observed by titanium dioxide photocatalysis within 30 min. The rate of degradation increased as initial carbamazepine concentration decreased, and the removal kinetics fit well with the Langmuir-Hinshelwood model. The addition of methanol, a radical scavenger, decreased carbamazepine removal, suggesting that the hydroxide radical played an important role during carbamazepine degradation. The addition of oxygen during titanium dioxide photocatalysis accelerated hydroxide radical production, thus improving mineralization activity. The photocatalytic degradation was more efficient at a higher pH, whereas the removal of carbamazepine and acridine (a major intermediate) were more efficient under aerobic conditions. The mineralization of carbamazepine during photocatalysis produced various ionic by-products such as ammonium and nitrate by way of nitrogen dioxide.

  16. Tetracalcium phosphate: Synthesis, properties and biomedical applications.

    Science.gov (United States)

    Moseke, C; Gbureck, U

    2010-10-01

    Monoclinic tetracalcium phosphate (TTCP, Ca(4)(PO(4))(2)O), also known by the mineral name hilgenstockite, is formed in the (CaO-P(2)O(5)) system at temperatures>1300 degrees C. TTCP is the only calcium phosphate with a Ca/P ratio greater than hydroxyapatite (HA). It appears as a by-product in plasma-sprayed HA coatings and shows moderate reactivity and concurrent solubility when combined with acidic calcium phosphates such as dicalcium phosphate anhydrous (DCPA, monetite) or dicalcium phosphate dihydrate (DCPD, brushite). Therefore it is widely used in self-setting calcium phosphate bone cements, which form HA under physiological conditions. This paper aims to review the synthesis and properties of TTCP in biomaterials applications such as cements, sintered ceramics and coatings on implant metals.

  17. Kampelite, Ba3Mg1.5Sc4(PO4)6(OH)3·4H2O, a new very complex Ba-Sc phosphate mineral from the Kovdor phoscorite-carbonatite complex (Kola Peninsula, Russia)

    Science.gov (United States)

    Yakovenchuk, Victor N.; Ivanyuk, Gregory Yu.; Pakhomovsky, Yakov A.; Panikorovskii, Taras L.; Britvin, Sergei N.; Krivovichev, Sergey V.; Shilovskikh, Vladimir V.; Bocharov, Vladimir N.

    2017-06-01

    Kampelite, Ba3Mg1.5Sc4(PO4)6(OH)3·4H2O, is a new Ba-Sc phosphate from the Kovdor phoscorite-carbonatite complex (Kola Peninsula, Russia). It is orthorhombic, Pnma, a = 11.256(1), b = 8.512(1), c = 27.707(4) Å, V = 2654.6(3) Å3 and Z = 4 (from powder diffraction data) or a = 11.2261(9), b = 8.5039(6), c = 27.699(2) Å, V = 2644.3(3) Å3 (from single-crystal diffraction data). The mineral was found in a void within the calcite-magnetite phoscorite (enriched in hydroxylapatite and Sc-rich baddeleyite) inside the axial zone of the Kovdor phoscorite-carbonatite pipe. Kampelite forms radiated aggregates (up to 1.5 mm in diameter) of platy crystals grown on the surfaces of crystals of quintinite-2H in close association with pyrite, bobierrite and quintinite-3R. Kampelite is colourless, with a pearly lustre and a white streak. The cleavage is perfect on {001}, the fracture is smooth. Mohs hardness is about 1. In transmitted light, the mineral is colourless without pleochroism or dispersion. Kampelite is biaxial + (pseudouniaxial), α ≈ β = 1.607(2), γ = 1.612(2) (589 nm), and 2V calc = 0°. The calculated and measured densities are 3.28 and 3.07(3) g·cm-3, respectively. The mean chemical composition determined by electron microprobe is: MgO 4.79, Al2O3 0.45, P2O5 31.66, K2O 0.34, Sc2O3 16.17, Mn2O3 1.62, Fe2O3 1.38, SrO 3.44, and BaO 29.81 wt%. The H2O content estimated from the crystal-structure refinement is 7.12 wt%, giving a total of 96.51 wt%. The empirical formula calculated on the basis of P = 6 apfu (atoms per formula unit) is (Ba2.62Sr0.45K0.10Ca0.06)Σ3.23Mg1.60Mn0.28(Sc3.15Fe3+ 0.23Al0.12)Σ3.50(PO4)6(OH)2.61·4.01H2O. The simplified formula is Ba3Mg1.5Sc4(PO4)6(OH)3·4H2O. The mineral easily dissolves in 10% cold HCl. The strongest X-ray powder-diffraction lines [listed as d in Å (I) (hkl)] are as follows: 15.80(100)(001), 13.86(45)(002), 3.184(18)(223), 3.129(19)(026), 2.756(16)(402), 2.688(24)(1010). The crystal structure of kampelite was refined to

  18. Effect of whitening toothpaste on titanium and titanium alloy surfaces

    National Research Council Canada - National Science Library

    Faria, Adriana Cláudia Lapria; Bordin, Angelo Rafael de Vito; Pedrazzi, Vinícius; Rodrigues, Renata Cristina Silveira; Ribeiro, Ricardo Faria

    2012-01-01

    .... Whitening toothpastes with peroxides are available for patients with high aesthetic requirements, but the effect of whitening toothpastes on titanium surfaces is not yet known, although titanium...

  19. UV photofunctionalization promotes nano-biomimetic apatite deposition on titanium

    Directory of Open Access Journals (Sweden)

    Saita M

    2016-01-01

    in the valleys and at the inclines of micro-roughened structures without affecting the existing micro-configuration. Micro-roughened titanium and apatite-deposited titanium surfaces had similar roughness values. The attachment, spreading, settling, proliferation, and alkaline phosphate activity of bone marrow-derived osteoblasts were promoted on apatite-coated titanium with photofunctionalization.Conclusion: UV-photofunctionalization of titanium enabled faster deposition of nanoscale biomimetic apatite, resulting in the improved biological capability compared to the similarly prepared apatite-deposited titanium without photofunctionalization. Photofunctionalization-assisted biomimetic apatite deposition may be a novel method to effectively enhance micro-roughened titanium surfaces without altering their microscale morphology. Keywords: nanotechnology, dental and orthopedic implants, superhydrophilic, hydrocarbon, osseointegration 

  20. Biofunctionalization of titanium for dental implant

    Directory of Open Access Journals (Sweden)

    Takao Hanawa

    2010-08-01

    Full Text Available Surface modification is an important and predominant technique for obtaining biofunction in metals for biomedical use including dentistry. One surface modification technique is a process that changes the surface composition, structure, and morphology of a material, leaving the bulk mechanical properties intact. A tremendous number of surface modification techniques to improve the hard tissue compatibility of titanium have been developed. Hydroxyapatite layer, titanium oxide layer, and calcium titanate layer with various morphologies are deposited using electrochemical treatment including micro-arc oxidation. Also, surface modification layers without hydroxyapatite and calcium phosphate are chemically formed that accelerate bone formation. Other approach is the immobilization of biofunctional molecules such as poly(ethylene glycol to the metal surface to control the adsorption of proteins and adhesion of cells, platelets, and bacteria. In the case of immobilization of biomolecules such as collagen and peptide, bone formation and soft tissue adhesion are improved.

  1. Zirconium-titanium placers of the Voronezh Anteclise: Types, epochs and factors of formation, and forecast

    Science.gov (United States)

    Savko, A. D.; Zvonarev, A. E.; Ivanov, D. A.

    2012-02-01

    The early and late Frasnian, Barremian-Aptian, Cenomanian, early Santonian, early Campanian, and Oligocene-Miocene epochs of the formation of various types of zirconium-titanium placers are distinguished in the Voronezh Anteclise. The factors of their formation are considered, and a forecast of prospecting has been made. Lower Frasnian sedimentary rocks occur in the southeast, where the placers are related to the ilmenite-bearing volcanosedimentary rocks of the Yastrebovo Sequence. The upper Frasnian productive quartz sand of the Petino Sequence occurs in the central part of the Voronezh Anteclise. The Barremian-Aptian productive quartz sand and kaolinite clay occur in the northern and northeastern parts of the anteclise (Ryazan and Lipetsk oblasts). The placers formed in the Cenomanian are known in the Tambov oblast in the northeast of the Voronezh Anteclise and are related to phosphate-bearing glauconite-quartz sand. The early Campanian phosphorite-glauconite-quartz formation is widespread in the northwest of the Voronezh Anteclise at the junction with the northeastern wall of the Dnieper-Donets Basin (Bryansk oblast). The Oligocene-Miocene epoch was characterized by quartz sands abundant in the northwestern and south-western areas. The formation of zirconium-titanium placers is controlled by structural-tectonic, facies, volcanic, paleogeographic, stratigraphic, and evolutional factors. The indispensable condition for heavy mineral concentration is existence of positive forms of underwater topography. These are mostly structural elements of the third and fourth orders on the slopes of the Voronezh Anteclise at the boundaries of the adjacent negative structures. As concerns the facies factor, the occurrence of coastal and shallow-water marine facies with alternating and medium hydrodynamic activity and predominance of sand fractions 0.25-0.05 mm are criteria of elevated concentration of heavy minerals in sand. One of the conditions providing concentration of heavy

  2. Inhibition effect of phosphate on the crystal grain growth of nanosized titania

    Institute of Scientific and Technical Information of China (English)

    FENG Xiaohui; LIE Jingze; LI Ping; ZHANG Yanfeng; WEI Yu

    2009-01-01

    The inhibitory effect of phosphate on the crystal grain growth of nanosized titania during high temperature calcination was investigated. Nanosized titanium dioxide powders prepared by hydrolysis of titanium tetrachloride were soaked in phosphate solutions with different con-centrations. The obtained powders calcined at various temperatures were characterized by X-ray diffraction (XRD), Fourier transform infra-red spectroscopy (FTIR), and X-ray photoelectronic spectroscopy (XPS). The grain size of the samples without phosphate treatment in-creased quickly when calcined at high temperatures, while the grain size of the samples with phosphate modification increased slowly when calcined at the same temperature. This phenomenon implies that phosphate treatment plays an important role in inhibiting the crystal grain growth of titania. The possible mechanism of the inhibition effect of phosphate on titania is discussed.

  3. Phosphate Biomineralization of Cambrian Microorganisms

    Science.gov (United States)

    McKay, David S.; Rozanov, Alexei Yu.; Hoover, Richard B.; Westall, Frances

    1998-01-01

    As part of a long term study of biological markers (biomarkers), we are documenting a variety of features which reflect the previous presence of living organisms. As we study meteorites and samples returned from Mars, our main clue to recognizing possible microbial material may be the presence of biomarkers rather than the organisms themselves. One class of biomarkers consists of biominerals which have either been precipitated directly by microorganisms, or whose precipitation has been influenced by the organisms. Such microbe-mediated mineral formation may include important clues to the size, shape, and environment of the microorganisms. The process of fossilization or mineralization can cause major changes in morphologies and textures of the original organisms. The study of fossilized terrestrial organisms can help provide insight into the interpretation of mineral biomarkers. This paper describes the results of investigations of microfossils in Cambrian phosphate-rich rocks (phosphorites) that were found in Khubsugul, Northern Mongolia.

  4. Control of Vertebrate Skeletal Mineralization by Polyphosphates

    Science.gov (United States)

    Omelon, Sidney; Georgiou, John; Henneman, Zachary J.; Wise, Lisa M.; Sukhu, Balram; Hunt, Tanya; Wynnyckyj, Chrystia; Holmyard, Douglas; Bielecki, Ryszard; Grynpas, Marc D.

    2009-01-01

    Background Skeletons are formed in a wide variety of shapes, sizes, and compositions of organic and mineral components. Many invertebrate skeletons are constructed from carbonate or silicate minerals, whereas vertebrate skeletons are instead composed of a calcium phosphate mineral known as apatite. No one yet knows why the dynamic vertebrate skeleton, which is continually rebuilt, repaired, and resorbed during growth and normal remodeling, is composed of apatite. Nor is the control of bone and calcifying cartilage mineralization well understood, though it is thought to be associated with phosphate-cleaving proteins. Researchers have assumed that skeletal mineralization is also associated with non-crystalline, calcium- and phosphate-containing electron-dense granules that have been detected in vertebrate skeletal tissue prepared under non-aqueous conditions. Again, however, the role of these granules remains poorly understood. Here, we review bone and growth plate mineralization before showing that polymers of phosphate ions (polyphosphates: (PO3−)n) are co-located with mineralizing cartilage and resorbing bone. We propose that the electron-dense granules contain polyphosphates, and explain how these polyphosphates may play an important role in apatite biomineralization. Principal Findings/Methodology The enzymatic formation (condensation) and destruction (hydrolytic degradation) of polyphosphates offers a simple mechanism for enzymatic control of phosphate accumulation and the relative saturation of apatite. Under circumstances in which apatite mineral formation is undesirable, such as within cartilage tissue or during bone resorption, the production of polyphosphates reduces the free orthophosphate (PO43−) concentration while permitting the accumulation of a high total PO43− concentration. Sequestering calcium into amorphous calcium polyphosphate complexes can reduce the concentration of free calcium. The resulting reduction of both free PO43− and free

  5. Preparation of calcium carbonate particles coated with titanium dioxide

    Institute of Scientific and Technical Information of China (English)

    Hai Lin; Ying-bo Dong; Le-yong Jiang

    2009-01-01

    The preparation of a new mineral composite material, calcium carbonate particles coated with titanium dioxide, was stud-ied. The mechanism of the preparation process was proposed. The new mineral composite material was made by the mechanochemi-eal method under the optimum condition that the mass ratio of calcium carbonate particles to titanium dioxide was 6.5:3.5. The mass ratios of two different types of titanium dioxide (anatase to rutile) and grinding media to grinded materials were 8:2 and 4:1 respec-tively, and the modified density was 60%. Under this condition, the new material was capable of forming after 120-min modification.The hiding power and oil absorption of this new material were 29.12 g/m~2 and 23.30%, respectively. The results show that the modi-fication is based on surface hydroxylation. After coating with titanium dioxide, the hiding power of calcium carbonate can be im-proved greatly. The new mineral composite materials can be used as the substitute for titanium dioxide.

  6. Ion adsorption on titanium surfaces exposed to a physiological solution

    Science.gov (United States)

    Frauchiger, L.; Taborelli, M.; Aronsson, B.-O.; Descouts, P.

    1999-04-01

    Changes in surface properties of titanium platelets exposed to a physiological solution (Hanks' solution) were studied by Auger electron spectroscopy and Attenuated Total Reflection Fourier Transform Infra Red spectroscopy for surface chemical composition analysis and by Scanning Force Microscopy for surface topography measurements. An adsorbed layer of calcium-phosphate was spontaneously formed on the titanium oxide surface and its thickness as well as the Ca/P ratio was found to increase with immersion time. After 71 days of immersion, the Ca/P ratio corresponded to that of brushite or monetite and after 6 months it was close to the value of hydroxyapatite. A higher Ca/P ratio was found for adsorption from solutions where the pH had been increased. After adsorption, the grains of the evaporated titanium substrate appeared slightly smoother because they were covered by a thin layer of calcium phosphate. A comparison between immersion in a Hanks' solution and solutions containing only phosphates or only calcium ions, showed that the presence of phosphates is necessary for the adsorption of Ca-ions.

  7. The use of titanium alloys for details of downhole hammers

    Science.gov (United States)

    Popelyukh, A. I.; Repin, A. A.; Alekseev, S. E.; Martyushev, N. V.; Drozdov, Yu Yu

    2016-04-01

    The influence of cementation technology of titanium alloy Ti-Al-Mn on its wear resistance is studied. It is established that after lubrication a friction pair with mineral oil the wear resistance of the cemented titanium alloy is comparable to wear resistance of the tempered steel 12HN3A, and in water medium surpasses it by 1.5 times. Decrease in the tendency to seizure with steel is the main reason for increase of wear resistance of titanium alloy. Industrial tests of the ASH43 hammer have shown that the use of titanium alloys for the manufacture of hammer strikers allows to increase impact capacity by 1.5 times and to increase drilling rate by 30 % compared to hammers with steel strikers.

  8. Osteoblastic response to pectin nanocoating on titanium surfaces

    DEFF Research Database (Denmark)

    Gurzawska, Katarzyna; Svava, Rikke; Yihua, Yu

    2014-01-01

    Osseointegration of titanium implants can be improved by organic and inorganic nanocoating of the surface. The aim of our study was to evaluate the effect of organic nanocoating of titanium surface with unmodified and modified pectin Rhamnogalacturonan-Is (RG-Is) isolated from potato and apple...... viability, bone matrix formation and mineralization was tested using SaOS-2 cells. Nanocoating with pectin RG-Is affected surface properties and in consequence changed the environment for cellular response. The cells cultured on surfaces coated with RG-Is from potato with high content of linear 1.4-linked...... galactose produced higher level of mineralized matrix compared with control surfaces and surfaces coated with RG-I with low content of linear 1.4-linked galactose. The study showed that the pectin RG-Is nanocoating not only changed chemical and physical titanium surface properties, but also specific coating...

  9. Adsorption of Phosphate on Variable Charge Soils

    Institute of Scientific and Technical Information of China (English)

    HUGUO-SONG; ZHUZU-XIANG; 等

    1992-01-01

    The study about the adsorption of phosphate on four variable charge soils and some minerals revealed that two stage adsorption appeared in the adsorption isothems of phosphate on 4 soils and there was a maximum adsorption on Al-oxide-typed surfaces between pH 3.5 to pH 5.5 as suspension pH changed from 2 to 9,but the adsorption amount of phosphate decreased continually as pH rose on Fe-oxide typed surfaces.The adsorption amount of phosphate and the maximum phosphate adsorption pH decreased in the order of yellow-red soil> lateritic red soil> red soil> paddy soil,which was coincided with the content order of amorphous Al oxide.The removement of organic matter and Fe oxide made the maximum phosphate adsorption pH rise from 4.0 to 5.0 and 4.5,respectively.The desorption curves with pH of four soils showed that phosphate desorbed least at pH 5.Generally the desorption was contrary to the adsorption with pH changing.There was a good accordance between adsorption or desorption and the concentration of Al in the suspension.The possible mechanisms of phosphate adsorption are discussed.

  10. Nanoscale Bonding between Human Bone and Titanium Surfaces: Osseohybridization

    Directory of Open Access Journals (Sweden)

    Jun-Sik Kim

    2015-01-01

    Full Text Available Until now, the chemical bonding between titanium and bone has been examined only through a few mechanical detachment tests. Therefore, in this study, a sandblasted and acid-etched titanium mini-implant was removed from a human patient after 2 months of placement in order to identify the chemical integration mechanism for nanoscale osseointegration of titanium implants. To prepare a transmission electron microscopy (TEM specimen, the natural state was preserved as much as possible by cryofixation and scanning electron microscope/focused ion beam (SEM-FIB milling without any chemical treatment. High-resolution TEM (HRTEM, energy dispersive X-ray spectroscopy (EDS, and scanning TEM (STEM/electron energy loss spectroscopic analysis (EELS were used to investigate the chemical composition and structure at the interface between the titanium and bone tissue. HRTEM and EDS data showed evidence of crystalline hydroxyapatite and intermixing of bone with the oxide layer of the implant. The STEM/EELS experiment provided particularly interesting results: carbon existed in polysaccharides, calcium and phosphorus existed as tricalcium phosphate (TCP, and titanium existed as oxidized titanium. In addition, the oxygen energy loss near edge structures (ELNESs showed a possibility of the presence of CaTiO3. These STEM/EELS results can be explained by structures either with or without a chemical reaction layer. The possible existence of the osseohybridization area and the form of the carbon suggest that reconsideration of the standard definition of osseointegration is necessary.

  11. Investigation of Corrosion Behavior of Bioactive Coverings on Commercially Pure Titanium and its Alloys

    Directory of Open Access Journals (Sweden)

    M.Yu. Gazizova

    2015-12-01

    Full Text Available A microporous and macroporous bioactive coatings on boimedical titanium alloys (VT1-0, VT6, Ti-6Al-7Nb were formed by a micro-arc oxidation method. The effect of the phase composition of microporous and macroporous coatings on corrosion behavior titanium and its alloys was investigated. The results show that phase composition of the coatings microporous presented only titanium oxides: anatase and rutile, at that the phase composition macroporous coatings consists of anatase, rutile and calcium phosphate compounds: tricalcium phosphate (TCP α-Ca3(PO42 and calcium deficient hydroxyapatite Ca9HPO4(PO45OH. Corrosion behavior of MAO coatings was investigated in solution 0.9 % NaCl using potentiodynamic polarization tests. The microporous coatings exhibited a more highest corrosion resistance than macroporous coatings, it is connected with containing calcium phosphate compounds in macroporous coatings.

  12. [Phosphate sensing and parathyroid gland].

    Science.gov (United States)

    Mizobuchi, Masahide; Suzuki, Taihei

    2012-10-01

    In the latter 1990s, phosphate, as well as calcium, has been shown to have a direct action on parathyroid function. Since then although many researchers have tried to detect the phosphate sensor in parathyroid gland, none has found it yet. In 2000s, the importance of FGF23 was revealed in patients with autosomal dominant hypophosphatemic rickets and then investigating the role of FGF23 in mineral metabolism has spread. FGF23 target organs comprise those that express coreceptor Klotho, such as kidney and parathyroid glands. While associations of calcium sensing receptor or vitamin D receptor with parathyroid function have been mainly investigated for parathyroid dysfunction, many efforts recently have made to study the effects of FGF23 on parathyroid glands.

  13. Machining of titanium alloys

    CERN Document Server

    2014-01-01

    This book presents a collection of examples illustrating the resent research advances in the machining of titanium alloys. These materials have excellent strength and fracture toughness as well as low density and good corrosion resistance; however, machinability is still poor due to their low thermal conductivity and high chemical reactivity with cutting tool materials. This book presents solutions to enhance machinability in titanium-based alloys and serves as a useful reference to professionals and researchers in aerospace, automotive and biomedical fields.

  14. Titanium allergy: A literature review

    Directory of Open Access Journals (Sweden)

    Manish Goutam

    2014-01-01

    Full Text Available Titanium has gained immense popularity and has successfully established itself as the material of choice for dental implants. In both medical and dental fields, titanium and its alloys have demonstrated success as biomedical devices. Owing to its high resistance to corrosion in a physiological environment and the excellent biocompatibility that gives it a passive, stable oxide film, titanium is considered the material of choice for intraosseous use. There are certain studies which show titanium as an allergen but the resources to diagnose titanium sensivity are very limited. Attention is needed towards the development of new and precise method for early diagnosis of titanium allergy and also to find out the alternative biomaterial which can be used in place of titanium. A review of available articles from the Medline and PubMed database was done to find literature available regarding titanium allergy, its diagnosis and new alternative material for titanium.

  15. Amine-intercalated α-zirconium phosphates as lubricant additives

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Huaping; Dai, Wei [Department of Mechanical Engineering, Texas A& M University, College Station, TX 77843 (United States); Kan, Yuwei; Clearfield, Abraham [Department of Chemistry, Texas A& M University, College Station, TX 77843 (United States); Liang, Hong, E-mail: hliang@tamu.edu [Department of Mechanical Engineering, Texas A& M University, College Station, TX 77843 (United States)

    2015-02-28

    In this study, three types of amines intercalated α-zirconium phosphate nanosheets with different interspaces were synthesized and examined as lubricant additives to a mineral oil. Results from tribological experiments illustrated that these additives improved lubricating performance. Results of rheological experiments showed that the viscosity of the mineral oil was effectively reduced with the addition of α-zirconium phosphate nanosheets. The two-dimensional structure, with larger interspaces, resulting from amine intercalation, exhibited improved effectiveness in reducing viscosity. This study demonstrates that the nanosheet structure of α-zirconium phosphates is effective in friction reduction. The manufacture of lubricants with tailored viscosity is possible by using different intercalators.

  16. Intermetallic communication in titanium(IV) ferrocenyldiketonates.

    Science.gov (United States)

    Dulatas, Lea T; Brown, Seth N; Ojomo, Edema; Noll, Bruce C; Cavo, Matthew J; Holt, Paul B; Wopperer, Matthew M

    2009-11-16

    A tetradentate bis(ferrocenyldiketonate) ligand, Fc(2)BobH(2), is prepared via Claisen condensation of acetylferrocene and 2,2'-biphenyldiacetyl chloride, and is metalated with titanium(IV) isopropoxide to give (Fc(2)Bob)Ti(O(i)Pr)(2) in good yield. The isopropoxide groups are replaced with di(4-nitrophenyl)phosphate groups on treatment with the corresponding acid, and with chlorides on treatment with trimethylsilyl chloride. Metathesis with catechol leads to the bis(o-hydroxyphenoxide) complex rather than the chelating catecholate complex. Hydrolysis selectively gives the mu-oxo trimer (Delta,Delta,Delta)/(Lambda,Lambda,Lambda)-{(Fc(2)Bob)Ti(mu-O)}(3). The solid-state structures of the mu-oxo trimer and the bis(o-hydroxyphenoxide) complex show that the ferrocene substituents are oriented proximal to the biphenyl backbone rather than pointed out toward the exogenous groups. The complexes show dramatic changes in color depending on the bound anions, ranging from the red isopropoxide (lambda(max) = 489 nm) to the green bis(di(4-nitrophenyl)phosphate) (lambda(max) = 653 nm). The oxidation potentials of the ferrocenes show modest shifts based on the titanium environment, but the redox potentials of the two ferrocenes are never separated by more than 60 mV. These results and those of density-functional theory (DFT) calculations indicate that the titanium interacts principally with the lowest unoccupied molecular orbital (LUMO) of the ferrocenyldiketonate and very little with its highest occupied molecular orbital (HOMO).

  17. Mineral oils

    Science.gov (United States)

    Furby, N. W.

    1973-01-01

    The characteristics of lubricants made from mineral oils are discussed. Types and compositions of base stocks are reviewed and the product demands and compositions of typical products are outlined. Processes for commercial production of mineral oils are examined. Tables of data are included to show examples of product types and requirements. A chemical analysis of three types of mineral oils is reported.

  18. Equilibrium relations in the system TiO{sub 2}/V{sub 2}O{sub 5}/P{sub 2}O{sub 5} and crystal structure of a NASICON-related vanadyl(V) titanium(IV) phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Titlbach, Sven; Hoffbauer, Wilfried [Institut fuer Anorganische Chemie der Universitaet Bonn, Gerhard-Domagk-Str. 1, D-53121 Bonn (Germany); Glaum, Robert, E-mail: rglaum@uni-bonn.de [Institut fuer Anorganische Chemie der Universitaet Bonn, Gerhard-Domagk-Str. 1, D-53121 Bonn (Germany)

    2012-12-15

    Vanadyl(V)-titanium-orthophosphate (V{sup V}O)Ti{sup IV}{sub 6}(PO{sub 4}){sub 9} is formed by solid state reactions in the temperature range 525{<=}{theta}{<=}780 Degree-Sign C. At higher temperature decomposition into V{sub 2}O{sub 5} and the hitherto unknown solid solution Ti(P{sub 1-x}V{sub x}){sub 2}O{sub 7} (0{<=}x{<=}0.23; 0.30{<=}x{<=}0.43) is observed. The process of phase formation has been monitored by MAS-NMR ({sup 31}P, {sup 51}V) spectroscopy. Equilibrium phase relations in the quaternary system TiO{sub 2}/VO{sub 2.5}/PO{sub 2.5} have been determined. A structure analysis from X-ray single-crystal data (P6{sub 3}/m (No. 176), Z=2; a=8.4438(3) A, c=22.215(1) A, 14 independent atoms, 87 variables, 2066 unique reflections, R1=0.032, wR2=0.084) shows the relationship of (V{sup V}O)Ti{sup IV}{sub 6}(PO{sub 4}){sub 9} to the NASICON structure family. In marked contrast to the other members of this family [Ti{sup IV}{sub 2}O{sub 9}] double-octahedra and strongly distorted tetrahedral [(V{sup V}=O)O{sub 3}] groups are observed besides isolated [Ti{sup IV}O{sub 6}] octahedra and phosphate tetrahedra. The structure model is in agreement with the results from MAS-NMR ({sup 31}P, {sup 51}V) spectroscopy. - Graphical abstract: (V{sup V}O)Ti{sup IV}{sub 6}(PO{sub 4}){sub 9} belongs to the NASICON structure family. Its structure contains [Ti{sup IV}{sub 2}O{sub 9}] double-octahedra and unprecedented, strongly distorted tetrahedral [(V{sup V}=O)O{sub 3}] groups, in stark contrast to other members of this family. The structure model is in agreement with the results from MAS-NMR ({sup 31}P, {sup 51}V) spectroscopy. Highlights: Black-Right-Pointing-Pointer Equilibrium relations for the subsolidus have been established for the system TiO{sub 2}/V{sub 2}O{sub 5}/P{sub 2}O{sub 5}. Black-Right-Pointing-Pointer Phase formation has been monitored by XRPD as well as by {sup 31}P- and {sup 51}-MAS-NMR. Black-Right-Pointing-Pointer A solid solution Ti(P{sub 1-x}V{sub x}){sub 2}O

  19. [Vascular Calcification - Pathological Mechanism and Clinical Application - . Regulation of mineral metabolism and mineralization by FGF23].

    Science.gov (United States)

    Fukumoto, Seiji

    2015-05-01

    Fibroblast growth factor 23 (FGF23) decreases serum phosphate by inhibiting proximal tubular phosphate reabsorption and intestinal phosphate absorption through the reduction of serum 1,25-dihydroxyvitamin D [1,25 (OH) (2)D] levels. Excessive actions of FGF23 cause hypophosphatemic diseases with impaired mineralization of bone. On the other hand, impaired actions of FGF23 result in hyperphosphatemic familial tumoral calcinosis characterized by hyperphosphatemia and high 1,25 (OH) (2)D levels. Ectopic calcification around large joints and in blood vessels can be observed in patients with this disease. Therefore, FGF23 plays essential roles in the regulation of bone mineralization and prevention of ectopic calcification.

  20. Phosphate homeostasis and disorders.

    Science.gov (United States)

    Manghat, P; Sodi, R; Swaminathan, R

    2014-11-01

    Recent studies of inherited disorders of phosphate metabolism have shed new light on the understanding of phosphate metabolism. Phosphate has important functions in the body and several mechanisms have evolved to regulate phosphate balance including vitamin D, parathyroid hormone and phosphatonins such as fibroblast growth factor-23 (FGF23). Disorders of phosphate homeostasis leading to hypo- and hyperphosphataemia are common and have clinical and biochemical consequences. Notably, recent studies have linked hyperphosphataemia with an increased risk of cardiovascular disease. This review outlines the recent advances in the understanding of phosphate homeostasis and describes the causes, investigation and management of hypo- and hyperphosphataemia.

  1. Deposit model for heavy-mineral sands in coastal environments: Chapter L in Mineral deposit models for resource assessment

    Science.gov (United States)

    Van Gosen, Bradley S.; Fey, David L.; Shah, Anjana K.; Verplanck, Philip L.; Hoefen, Todd M.

    2014-01-01

    This report provides a descriptive model of heavy-mineral sands, which are sedimentary deposits of dense minerals that accumulate with sand, silt, and clay in coastal environments, locally forming economic concentrations of the heavy minerals. This deposit type is the main source of titanium feedstock for the titanium dioxide (TiO2) pigments industry, through recovery of the minerals ilmenite (Fe2+TiO3), rutile (TiO2), and leucoxene (an alteration product of ilmenite). Heavy-mineral sands are also the principal source of zircon (ZrSiO4) and its zirconium oxide; zircon is often recovered as a coproduct. Other heavy minerals produced as coproducts from some deposits are sillimanite/kyanite, staurolite, monazite, and garnet. Monazite [(Ce,La,Nd,Th)PO4] is a source of rare earth elements as well as thorium, which is used in thorium-based nuclear power under development in India and elsewhere.

  2. Osteoblastic response to pectin nanocoating on titanium surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Gurzawska, Katarzyna, E-mail: kagu@sund.ku.dk [Research Center for Ageing and Osteoporosis, Departments of Medicine and Diagnostics, Copenhagen University Hospital Glostrup, Ndr. Ringvej 57, 2600 Glostrup (Denmark); Institute of Odontology, Faculty of Health and Medical Sciences, University of Copenhagen, Nørre Allé 20, 2200 Copenhagen N (Denmark); Svava, Rikke [Department of Plant Environment Sciences, Faculty of Life Sciences, University of Copenhagen, Thorvaldsensvej 40, 1871 Frederiksberg C (Denmark); Copenhagen Center for Glycomics, Institute for Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200 Copenhagen N (Denmark); Yihua, Yu; Haugshøj, Kenneth Brian [Microtechnology and Surface Analysis, Danish Technological Institute, Gregersensvej 8, 2630 Taastrup (Denmark); Dirscherl, Kai [Dansk Fundamental Metrologi A/S, Matematiktorvet 307, 2800 Lyngby (Denmark); Levery, Steven B. [Copenhagen Center for Glycomics, Institute for Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200 Copenhagen N (Denmark); Byg, Inge [Department of Plant Environment Sciences, Faculty of Life Sciences, University of Copenhagen, Thorvaldsensvej 40, 1871 Frederiksberg C (Denmark); Damager, Iben [Novozymes A/S, Krogshoejvej 36, 2880 Bagsvaerd (Denmark); Nielsen, Martin W. [Department of Systems Biology, Technical University of Denmark, Matematiktorvet, Building 301, Kgs. Lyngby DK-2800 (Denmark); Jørgensen, Bodil [Department of Plant Environment Sciences, Faculty of Life Sciences, University of Copenhagen, Thorvaldsensvej 40, 1871 Frederiksberg C (Denmark); Jørgensen, Niklas Rye [Research Center for Ageing and Osteoporosis, Departments of Medicine and Diagnostics, Copenhagen University Hospital Glostrup, Ndr. Ringvej 57, 2600 Glostrup (Denmark); and others

    2014-10-01

    Osseointegration of titanium implants can be improved by organic and inorganic nanocoating of the surface. The aim of our study was to evaluate the effect of organic nanocoating of titanium surface with unmodified and modified pectin Rhamnogalacturonan-Is (RG-Is) isolated from potato and apple with respect to surface properties and osteogenic response in osteoblastic cells. Nanocoatings on titanium surfaces were evaluated by scanning electron microscopy, contact angle measurements, atomic force microscopy, and X-ray photoelectron spectroscopy. The effect of coated RG-Is on cell adhesion, cell viability, bone matrix formation and mineralization was tested using SaOS-2 cells. Nanocoating with pectin RG-Is affected surface properties and in consequence changed the environment for cellular response. The cells cultured on surfaces coated with RG-Is from potato with high content of linear 1.4-linked galactose produced higher level of mineralized matrix compared with control surfaces and surfaces coated with RG-I with low content of linear 1.4-linked galactose. The study showed that the pectin RG-Is nanocoating not only changed chemical and physical titanium surface properties, but also specific coating with RG-Is containing high amount of galactan increased mineralized matrix formation of osteoblastic cells in vitro. - Highlights: • Surface nanocoating with plant-derived Rhamnogalacturonan-I (RG-I) is proposed. • Titanium surface became more hydrophilic after RG-Is nanocoating. • RG-Is with high galactose content resulted in high level of mineralized matrix. • RG-I is a new candidate for improvement of bone healing and osseointegration.

  3. Physics and chemistry of minerals under laser processing

    Science.gov (United States)

    Kotova, O.; Leonenko, N.

    2016-04-01

    New experimental data of the influence of laser irradiation on the phase composition minerals of bauxite and red mud and their technological features have been represented. The mechanisms of formation of micro- and nanophases on mineral surfaces under the influence of laser irradiation were shown. It is underlined that changes of condition of surface atoms, concentration of metals, agglomeration of titanium minerals and new phase formation occurred under laser irradiation on bauxites and red mud.

  4. Surface modification of titanium and titanium alloys by ion implantation.

    Science.gov (United States)

    Rautray, Tapash R; Narayanan, R; Kwon, Tae-Yub; Kim, Kyo-Han

    2010-05-01

    Titanium and titanium alloys are widely used in biomedical devices and components, especially as hard tissue replacements as well as in cardiac and cardiovascular applications, because of their desirable properties, such as relatively low modulus, good fatigue strength, formability, machinability, corrosion resistance, and biocompatibility. However, titanium and its alloys cannot meet all of the clinical requirements. Therefore, to improve the biological, chemical, and mechanical properties, surface modification is often performed. In view of this, the current review casts new light on surface modification of titanium and titanium alloys by ion beam implantation.

  5. Chloroquine Phosphate Oral

    Science.gov (United States)

    Chloroquine phosphate is in a class of drugs called antimalarials and amebicides. It is used to prevent and treat ... Chloroquine phosphate comes as a tablet to take by mouth. For prevention of malaria in adults, one dose is ...

  6. Glucose-6-phosphate dehydrogenase

    Science.gov (United States)

    ... medlineplus.gov/ency/article/003671.htm Glucose-6-phosphate dehydrogenase test To use the sharing features on this page, please enable JavaScript. Glucose-6-phosphate dehydrogenase (G6PD) is a protein that helps red ...

  7. Investigation on the preparation of metakaolin-supported titanium mineral admixture with photocatalytic activity%高岭土负载钛制备具有光催化活性矿物掺合料的研究

    Institute of Scientific and Technical Information of China (English)

    张旭; 严云; 谢斐琳; 付丽; 胡志华

    2013-01-01

    A new process for preparing metakaolin-supported titania with the feature of both photocatalytic and pozzolanic activity by so called single calcination method was investigated.The ground pyrite tailing was mixed with the titania sol by sol-gel method firstly and then calcining the mixture with the optimum calcination regime by which could turn the kaolin into metakaolin-supported titania which has both good pozzolanic activity and photocatalytic performance.The effect of metakaolin-supported titania mineral admixture's dosage,load time on the of cement slurry has been investigated.The results show that the optimum calcination regime was 750 ℃for 2 h;the optimum loading time was 2 h;the optimum mineral admixture's dosage was 1 5%.The 7 d pozzo-lanic activity index of the metakaolin-supported titania mineral admixture can reach up to 1 1 3%.The photocata-lytic degradation efficiency on the MB of the admixture was high up to 93. 5% with the initial concentration of the MB was 1 5 mg/L.Micro-analysis was examined by XRD,ABS and TAM.The crystal form of titania sup-ported on the metakaolin powder was anatase and had a good crystallinity.The metakaolin-supported titania mineral admixture fabricated by this method demonstrates both a good photocatalytic,self-cleaning effect and excellent pozzolanic activity while incorporating into cementitious materials.%将溶胶-凝胶法制备的钛溶胶负载到硫铁矿尾矿上,采用一步煅烧法把尾矿转化为具有一定火山灰活性和光催化性的负载钛偏高岭土,并用它作为掺合料掺加到了水泥基体中。研究了负载时间、煅烧制度及负载钛量对该掺合料对水泥基材料的力学性能、早期水化行为及光催化性能的影响。结果表明,最佳负载时间为2 h,最佳煅烧制度是750℃×2 h,TiO2的晶型为结晶度较好的锐钛矿型。掺入水泥中最佳掺量为15%,7 d 活性指数达到113%,此时水化热低。高岭土中最佳负载钛量为7.5%,此时,0

  8. Bone reaction adjacent to microplasma-sprayed calcium phosphate-coated oral implants subjected to an occlusal load, an experimental study in the dog

    NARCIS (Netherlands)

    Junker, R.; Manders, P.J.D.; Wolke, J.G.C.; Borisov, Y.; Braceras, I.; Jansen, J.A.

    2011-01-01

    BACKGROUND: A new microplasma spraying equipment (MSE) to deposit calcium phosphate (CaP) ceramic coatings onto titanium substrates has been developed. With this system, it is possible to spray fine particles and to apply textured hydroxylapatite coatings onto titanium surfaces. Moreover, due to the

  9. Bone reaction adjacent to microplasma-sprayed calcium phosphate-coated oral implants subjected to an occlusal load, an experimental study in the dog

    NARCIS (Netherlands)

    Junker, R.; Manders, P.J.D.; Wolke, J.G.C.; Borisov, Y.; Braceras, I.; Jansen, J.A.

    2011-01-01

    BACKGROUND: A new microplasma spraying equipment (MSE) to deposit calcium phosphate (CaP) ceramic coatings onto titanium substrates has been developed. With this system, it is possible to spray fine particles and to apply textured hydroxylapatite coatings onto titanium surfaces. Moreover, due to the

  10. Enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium.

    Science.gov (United States)

    Zhu, Wei; Teel, George; O'Brien, Christopher M; Zhuang, Taisen; Keidar, Michael; Zhang, Lijie Grace

    2015-01-01

    Surface modification of titanium for use in orthopedics has been explored for years; however, an ideal method of integrating titanium with native bone is still required to this day. Since human bone cells directly interact with nanostructured extracellular matrices, one of the most promising methods of improving titanium's osseointegration involves inducing bio-mimetic nanotopography to enhance cell-implant interaction. In this regard, we explored an approach to functionalize the surface of titanium by depositing a thin film of textured titanium nanoparticles via a cathodic arc discharge plasma. The aim is to improve human bone marrow mesenchymal stem cell (MSC) attachment and differentiation and to reduce deleterious effects of more complex surface modification methods. Surface functionalization was analyzed by scanning electron microscopy, atomic force microscopy, contact angle testing, and specific protein adsorption. Scanning electron microscopy and atomic force microscopy examination demonstrate the deposition of titanium nanoparticles and the surface roughness change after coating. The specific fibronectin adsorption was enhanced on the modified titanium surface that associates with the improved hydrophilicity. MSC adhesion and proliferation were significantly promoted on the nanocoated surface. More importantly, compared to bare titanium, greater production of total protein, deposition of calcium mineral, and synthesis of alkaline phosphatase were observed from MSCs on nanocoated titanium after 21 days. The method described herein presents a promising alternative method for inducing more cell favorable nanosurface for improved orthopedic applications.

  11. A spanish mineral of zirconium and hafnium. Separation of the two elements by liquid-liquid extraction, using tributyl phosphate as chelating agent; Beneficio de un mineral espanol de circonio-hafnio. Separacion de ambos elementos por extraccion liquido-liquido, empleando fosfato de tributilo como agente de quelacion

    Energy Technology Data Exchange (ETDEWEB)

    Ruiz Sanchez, F.; Cruz Castillo, F. de la; Fernandez Cellini, R.

    1962-07-01

    The zirconium and Hafnium oxides are obtained from a Spanish mineral of zircon with an average contest of 55% in ZrO{sub 2}-HfO{sub 2}. An alkaline fusion to open the mineral, followed by a purification by crystallization as (Zr O-Hf O)Cl{sub 2} H{sub 2}O or as (Zr-Hf) (SO{sub 4}){sub 2}. 4H{sub 2}O, is used. A discussion of the best experimental conditions for opening the mineral and of the purification method is made. (Author) 45 refs.

  12. Effect of surface treatment of titanium posts on the tensile bond strength

    NARCIS (Netherlands)

    Schmage, P; Sohn, J; Ozcan, M; Nergiz, [No Value

    2006-01-01

    Objectives. Retention of composite resins to metal can be improved when metal surfaces are conditioned. The purpose of this investigation was to investigate the effect of two conditioning treatments on the tensile bond strength of four resin-based luting cements and zinc phosphate cement to titanium

  13. Why nature chose phosphates.

    Science.gov (United States)

    Westheimer, F H

    1987-03-06

    Phosphate esters and anhydrides dominate the living world but are seldom used as intermediates by organic chemists. Phosphoric acid is specially adapted for its role in nucleic acids because it can link two nucleotides and still ionize; the resulting negative charge serves both to stabilize the diesters against hydrolysis and to retain the molecules within a lipid membrane. A similar explanation for stability and retention also holds for phosphates that are intermediary metabolites and for phosphates that serve as energy sources. Phosphates with multiple negative charges can react by way of the monomeric metaphosphate ion PO3- as an intermediate. No other residue appears to fulfill the multiple roles of phosphate in biochemistry. Stable, negatively charged phosphates react under catalysis by enzymes; organic chemists, who can only rarely use enzymatic catalysis for their reactions, need more highly reactive intermediates than phosphates.

  14. INFLUENCE OF THE COMPOSITION OF PHOSPHATE ROCK ON THE AMOUNT OF WATER-INSOLUBLE PHOSPHATE IMPURITIES IN SEMI-HYDRATE PHOSPHOGYPSUM

    Directory of Open Access Journals (Sweden)

    Nora Kybartiene

    2015-03-01

    Full Text Available In this work a chemical and mineral composition of phosphate rock and phosphogypsum was investigated in order to identify which impurities of phosphate rock prevent natural phosphates from decomposing in full during the production of phosphoric acid and increase the amount of water-insoluble phosphate impurities in phosphogypsum. The analysis of X-ray diffraction (XRF, X-ray fluorescence (XRD, scanning electron microscopy with energy dispersive X-Ray spectrometry (SEM-EDS and granulometry was carried out. The results showed that phosphate rocks (Kovdor and Kirovsk apatites and the semi-hydrate phosphogypsums differ by their chemical composition. The apatites and phosphogypsums differ in the amount of the major components, as well as other components (MgO, Al2O3, SrO, BaO, ZrO2, Ln2O3. In phosphate rock, Ln2O3 can be found in the composition of the mineral monazite. The SEM-EDS analysis revealed that the minerals of the apatite group and monazite form aggregate crystals. Monazite dissolves in sulphuric and phosphoric acids very marginal, therefore it prevents the apatites from full decomposition, thus influencing the quantity of insoluble phosphates in semi-hydrate phosphogypsum. The higher is the amount of minerals containing Ln2O3 in phosphate rock, the more water-insoluble phosphates remain in phosphogypsum. It was found that influence of Ln2O3 impurity is significant higher than influence of particles size of apatite.

  15. Physics and chemistry of producing silicon-hydroxylapatite-titanium composite materials

    Science.gov (United States)

    Golovanova, O. A.; Zayts, A. V.; Panova, T. V.; Frangulyan, T. S.

    2015-04-01

    In the research, Si-HA poweders have been synthesized using SBF solution with different content of silicon. It was found that all the samples synthesized from the model solution of extracellular fluid under varying concentration of silicate ions are single-phase and repesent hydroxyapatite. The nature of the reagent containing SiO4-4 ions does not affect the hydroxyapatite structure. In the study of the surface and morphological characteristics of the phosphate coatings modified by silicon ions, it was found that as the degree of phosphate calcium substitution by SiO4-4 ions increases, the surface wettability on the titanium substrates deteriorates and cohesive energy decreases. It is shown that the titanium coating is formed in three stages. After irradiation of titanium substrates coated with Si-HA, the crystals can keep growing and the surface can keep regenerating.

  16. Adherent apatite coating on titanium substrate using chemical deposition.

    Science.gov (United States)

    Rohanizadeh, R; LeGeros, R Z; Harsono, M; Bendavid, A

    2005-03-15

    Plasma-sprayed "HA" coatings on commercial orthopedic and dental implants consist of mixtures of calcium phosphate phases, predominantly a crystalline calcium phosphate phase, hydroxyapatite (HA) and an amorphous calcium phosphate (ACP) with varying HA/ACP ratios. Alternatives to the plasma-spray method are being explored because of some of its disadvantages. The purpose of this study was to deposit an adherent apatite coating on titanium substrate using a two-step method. First, titanium substrates were immersed in acidic solution of calcium phosphate resulting in the deposition of a monetite (CaHPO4) coating. Second, the monetite crystals were transformed to apatite by hydrolysis in NaOH solution. Composition and morphology of the initial and final coatings were identified using X-ray diffraction (XRD), Scanning Electron Microscopy, and Energy Dispersive Spectroscopy (EDS). The final coating was porous and the apatite crystals were agglomerated and followed the outline of the large monetite crystals. EDS revealed the presence of calcium and phosphorous elements on the titanium substrate after removing the coating using tensile or scratching tests. The average tensile bond of the coating was 5.2 MPa and cohesion failures were observed more frequently than adhesion failures. The coating adhesion measured using scratch test with a 200-microm-radius stylus was 13.1N. Images from the scratch tracks demonstrated that the coating materials were squashed without fracturing inside and/or at the border of the tracks until the failure point of the coating. In conclusion, this study showed the potential of a chemical deposition method for depositing a coating consisting of either monetite or apatite. This method has the advantage of producing a coating with homogenous composition on even implants of complex geometry or porosity. This method involves low temperatures and, therefore, can allow the incorporation of growth factors or biogenic molecules.

  17. Atomic structure of intracellular amorphous calcium phosphate deposits.

    Science.gov (United States)

    Betts, F; Blumenthal, N C; Posner, A S; Becker, G L; Lehninger, A L

    1975-06-01

    The radial distribution function calculated from x-ray diffraction of mineralized cytoplasmic structures isolated from the hepatopancreas of the blue crab (Callinectes sapidus) is very similar to that previously found for synthetic amorphous calcium phosphate. Both types of mineral apparently have only short-range atomic order, represented as a neutral ion cluster of about 10 A in longest dimension, whose probable composition is expressed by the formula Ca9(PO4)6. The minor differences observed are attributed to the presence in the biological mineral of significant amounts of Mg-2+ and ATP. Synthetic amorphous calcium phosphate in contact with a solution containing an amount of ATP equivalent to that of the biological mineral failed to undergo conversion to the thermodynamically more stable hydroxyapatite. The amorphous calcium phosphate of the cytoplasmic mineral granules is similarly stable, and does not undergo conversion to hydroxyapatite, presumably owing to the presence of ATP and Mg-2+, known in inhibitors of the conversion process. The physiological implications of mineral deposits consisting of stabilized calcium phosphate ion clusters are discussed.

  18. Oxygen Extraction from Minerals

    Science.gov (United States)

    Muscatello, Tony

    2017-01-01

    Oxygen, whether used as part of rocket bipropellant or for astronaut life support, is a key consumable for space exploration and commercialization. In Situ Resource Utilization (ISRU) has been proposed many times as a method for making space exploration more cost effective and sustainable. On planetary and asteroid surfaces the presence of minerals in the regolith that contain oxygen is very common, making them a potential oxygen resource. The majority of research and development for oxygen extraction from minerals has been for lunar regolith although this work would generally be applicable to regolith at other locations in space. This presentation will briefly survey the major methods investigated for oxygen extraction from regolith with a focus on the current status of those methods and possible future development pathways. The major oxygen production methods are (1) extraction from lunar ilmenite (FeTiO3) with either hydrogen or carbon monoxide, (2) carbothermal reduction of iron oxides and silicates with methane, and (3) molten regolith electrolysis (MRE) of silicates. Methods (1) and (2) have also been investigated in a two-step process using CO reduction and carbon deposition followed by carbothermal reduction. All three processes have byproducts that could also be used as resources. Hydrogen or carbon monoxide reduction produce iron metal in small amounts that could potentially be used as construction material. Carbothermal reduction also makes iron metal along with silicon metal and a glass with possible applications. MRE produces iron, silicon, aluminum, titanium, and glass, with higher silicon yields than carbothermal reduction. On Mars and possibly on some moons and asteroids, water is present in the form of mineral hydrates, hydroxyl (-OH) groups on minerals, andor water adsorbed on mineral surfaces. Heating of the minerals can liberate the water which can be electrolyzed to provide a source of oxygen as well. The chemistry of these processes, some key

  19. HA coating on titanium with nanotubular anodized TiO2 intermediate layer via electrochemical deposition

    Institute of Scientific and Technical Information of China (English)

    WANG Yue-qin; TAO Jie; WANG Ling; HE Ping-ting; WANG Tao

    2008-01-01

    Hydroxyapatite (HA) coating has been prepared on titanium substrate through an electrochemical deposition approach.In order to improve the bonding strength between HA coating and Ti substrate,a well oriented and uniform titanium oxide nanotube array on the surface of titanium substrate was applied by means of anodic oxidation pre-treatment.Then the calcium hydrogen phosphate (CaHPO4-2H2O,DCPD) coating,as the precursor of hydroxyapatite coating,was electrodeposited on the anodized Ti.At the initial stage of electro-deposition,the DCPD crystals,in nanometer precipitates,are anchored in and between the tubes.With increasing the deposition time,the nanometer DCPD crystals are connected together to form a continuous coating on titanium oxide nanotube array.Finally,the DCPD coating is converted into hydroxyapatite one simply by being immersed in alkaline solution.

  20. Effect of amorphous fluorinated coatings on photocatalytic properties of anodized titanium surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Persico, Federico [Dipartimento di Chimica, Materiali e Ingegneria Chimica “Giulio Natta”, Politecnico di Milano, via Mancinelli 7, 20131, Milano (Italy); Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali, Via G. Giusti, 9, 50121 Firenze (Italy); Sansotera, Maurizio, E-mail: maurizio.sansotera@polimi.it [Dipartimento di Chimica, Materiali e Ingegneria Chimica “Giulio Natta”, Politecnico di Milano, via Mancinelli 7, 20131, Milano (Italy); Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali, Via G. Giusti, 9, 50121 Firenze (Italy); Diamanti, Maria Vittoria [Dipartimento di Chimica, Materiali e Ingegneria Chimica “Giulio Natta”, Politecnico di Milano, via Mancinelli 7, 20131, Milano (Italy); Magagnin, Luca; Venturini, Francesco; Navarrini, Walter [Dipartimento di Chimica, Materiali e Ingegneria Chimica “Giulio Natta”, Politecnico di Milano, via Mancinelli 7, 20131, Milano (Italy); Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali, Via G. Giusti, 9, 50121 Firenze (Italy)

    2013-10-31

    The photocatalytic activity promoted by anodized titanium surfaces coated with different amorphous perfluoropolymers was evaluated. A copolymer between tetrafluoroethylene and perfluoro-4-trifluoromethoxy-1,3-dioxole and two perfluoropolyethers containing ammonium phosphate and triethoxysilane functionalities, respectively, were tested as coating materials. These coatings revealed good adhesion to the anodized titanium substrate and conferred to it both hydrophobicity and oleophobicity. The photocatalytic activity of the coating on anodized titanium was evaluated by monitoring the degradation of stearic acid via Infrared spectroscopy. The degradation rate of stearic acid was reduced but not set to zero by the presence of the fluorinated coatings, leading to the development of advanced functional coatings. The morphological variations of the coatings as a result of photocatalysis were also determined by atomic force microscopy. - Highlights: • Coated anodized titanium surfaces show a decreased wettability. • Evaluation of the stability of perfluorinated coatings towards photocatalysis. • Amorphous perfluorinated coatings do not hinder photocatalytic activity.

  1. High-temperature Titanium Alloys

    Directory of Open Access Journals (Sweden)

    A.K. Gogia

    2005-04-01

    Full Text Available The development of high-temperature titanium alloys has contributed significantly to the spectacular progress in thrust-to-weight ratio of the aero gas turbines. This paper presents anoverview on the development of high-temperature titanium alloys used in aero engines and potential futuristic materials based on titanium aluminides and composites. The role of alloychemistry, processing, and microstructure, in determining the mechanical properties of titanium alloys is discussed. While phase equilibria and microstructural stability consideration haverestricted the use of conventional titanium alloys up to about 600 "C, alloys based on TiPl (or,, E,AINb (0, TiAl (y, and titaniumltitanium aluminides-based composites offer a possibility ofquantum jump in the temperature capability of titanium alloys.

  2. Molecular mechanisms of crystallization impacting calcium phosphate cements

    OpenAIRE

    2010-01-01

    The biomineral calcium hydrogen phosphate dihydrate (CaHPO4·2H2O), known as brushite, is a malleable material that both grows and dissolves faster than most other calcium minerals, including other calcium phosphate phases, calcium carbonates and calcium oxalates. Within the body, this ready formation and dissolution can play a role in certain diseases, such as kidney stone and plaque formation. However, these same properties, along with brushite’s excellent biocompatibility, can be used to gr...

  3. Hydrolytically stable titanium-45

    DEFF Research Database (Denmark)

    Severin, Gregory; Fonslet, Jesper; Zhuravlev, Fedor

    2014-01-01

    Introduction Titanium-45, a candidate PET isotope, is under-employed largely because of the challenging aqueous chemistry of Ti(IV). The propensity for hydrolysis of Ti(IV) compounds makes radio-labeling difficult and excludes 45Ti from use in bio-conjugate chemistry. This is unfortunate because...... metal-based chemotherapeutics such as cisplatin. The aim of our work has been to produce the radioactive analogue of one of these Ti(IV)-salan compounds, Ti-salan-dipic [2], which has hydro-lytic stability on the order of weeks. Not only will this allow us to shed some light on the still un......-known mechanism of antiproliferative action of titanium-based chemotherapeutics, but it will also make progress toward bioconjugate 45Ti PET tracers. In the current abstract, we present some of the methods we are using to separate 45Ti from irradiated Sc, and subsequent labeling conditions. Material and Methods...

  4. Titanium Carbide: Nanotechnology, Properties, Application

    OpenAIRE

    Galevsky, G. V.; Rudneva, V. V.; Garbuzova, A. K.; Valuev, Denis Viktorovich

    2015-01-01

    The paper develops scientific and technological bases for fabrication of titanium carbide which is a nanocomponent of composite materials. The authors determine optimum technology specifications and the main titanium carbide properties: fineness of titaniferous raw materials, carbide-forming agent quantity, set temperature of plasma flow, tempering temperature, titanium carbide yield, productivity, specific surface, size and shape of particles. The paper includes equations to describe how the...

  5. Enhanced osteoblast functions on anodized titanium with nanotube-like structures.

    Science.gov (United States)

    Yao, Chang; Slamovich, Elliott B; Webster, Thomas J

    2008-04-01

    Previous studies have demonstrated increased osteoblast (bone-forming cells) adhesion on titanium and Ti-6Al-4V anodized to possess nanometer features compared with their unanodized counterparts. In this study, osteoblast long-term functions (specifically, synthesis of intracellular proteins, synthesis of intracellular collagen, alkaline phosphatase activity, and deposition of calcium-containing minerals) were determined on titanium anodized to possess either heterogeneous nanoparticles or ordered nanotubes. Titanium was anodized in dilute hydrofluoric acid at 20 V for 20 min to possess nanotubes, while titanium was anodized at 10 V for 20 min to possess nanoparticles. Most importantly, results showed that calcium deposition significantly increased on anodized titanium with nanotube-like structures compared with unanodized titanium and anodized titanium with nanoparticulate structures after 21 days of osteoblast culture. In this manner, the results of the present in vitro study indicated that anodization might be a promising quick and inexpensive method to modify the surface of titanium-based implants to induce better bone cell functions important for orthopedic applications.

  6. Titanium Nitride Cermets

    Science.gov (United States)

    1952-07-01

    C ermets 7 Effect of Amount of Metal on Strength of TiN-Ni-Cr....26 Cerme ts S Effect of Amount of Metal on Strength of TiN-Co-Cr....27 Cermets 9...Figures 7 and 8. Titanium Nitride-Nickel-Chromium Cerme ts From Figure 7, it can be seen that 2900OF was the better firing temperature. The 20% metal

  7. Discussion about magnesium phosphating

    Directory of Open Access Journals (Sweden)

    P. Pokorny

    2016-07-01

    Full Text Available The paper describes results from recently published research focused on production of non-conventional magnesium phosphate Mg3(PO42・4H2O – bobierrite, or MgHPO4・3H2O – newberyite coating for both magnesium alloys and/or mild steel. This new kind of coating is categorized in the context of current state of phosphating technology and its potential advantages and crystal structure is discussed. At the same time, the suitable comparison techniques for magnesium phosphate coating and conventional zinc phosphate coating are discussed.

  8. Titanium Carbide: Nanotechnology, Properties, Application

    Science.gov (United States)

    Galevsky, G. V.; Rudneva, V. V.; Garbuzova, A. K.; Valuev, D. V.

    2015-09-01

    The paper develops scientific and technological bases for fabrication of titanium carbide which is a nanocomponent of composite materials. The authors determine optimum technology specifications and the main titanium carbide properties: fineness of titaniferous raw materials, carbide-forming agent quantity, set temperature of plasma flow, tempering temperature, titanium carbide yield, productivity, specific surface, size and shape of particles. The paper includes equations to describe how the major specifications of the fabrication technique influence the content of titanium carbide and free carbon in the end product.

  9. 生长微环境下原位矿化磷酸钙诱导的细胞死亡%Cell Death Induced by In Situ Mineralized Calcium Phosphate in Growth Microenvironment

    Institute of Scientific and Technical Information of China (English)

    刘朋; 陈燕; 王广川; 王本; 徐旭荣; 唐睿康

    2013-01-01

    The correlation of calcium phosphate quantity and their lethal effect on human osteosarcoma cells in growth microenvironment was investigated.The calcium phosphate nanoparticles (CaP-NPS) were in situ generated by adding calcium solution to cell culture media.The media with different amounts of CaP-NPS were prepared by suspending the obtained CaP-NPS into cell culture solutions.The viability of human osteosarcoma cells cultured in the media was examined by MTT method.We found that CaP-NPS induced death of the cocultured cells depending on their amounts.MTT assay revealed that CaP-NPS could obviously reduce the cell viability by inducing cell death when their quantity was above the threshold 240 μg ·mL-1.The transmission electron microscopy (TEM) results revealed that lots of CaP-NPS were observed in cytoplasm of cocultured cells when the concentration of CaP-NPS was >240 μg·mL-1.In contrast,no CaP-NPS was found within the cocultured cells when the concentration of CaP-NPS was <240 μg· mL-1.Our results implied that 240 μg·mL-1 CaP-NPS was a critical point for cell viability,exceeding which would cause severely cell death because it exceeded the limit of cell self-clarify or tolerant ability.This study may provide a guide for the CaP-NPS applications in medical engineering such as tissue engineering,drug delivery,and gene transfection.%本文主要研究了不同量的磷酸钙在生长环境下对骨肉瘤细胞死亡的影响.通过在无钙培养基中加入氯化钙原位合成得到所需磷酸钙颗粒,然后用无钙磷培养基按照不同的比例稀释所得磷酸钙颗粒.MTT结果表明,24 h后的细胞凋亡与培养基中磷酸钙的量有关.当浓度超过240 μg·mL-1时,细胞出现大量死亡.细胞超薄切片结果也表明,当磷酸钙浓度超过240 μg·mL-1时,可以观察到有大量磷酸钙存在于细胞内;而磷酸钙浓度低于240μg·mL-1时,细胞内观察不到磷酸钙的存在.这些结果表明:240 μg·mL-1对

  10. Effects of Soluble Phosphate on Phosphate-Solubilizing Characteristics and Expression of gcd Gene in Pseudomonas frederiksbergensis JW-SD2.

    Science.gov (United States)

    Zeng, Qingwei; Wu, Xiaoqin; Wen, Xinyi

    2016-02-01

    Phosphate-solubilizing bacteria have the ability of solubilizing mineral phosphate in soil and promoting growth of plants, but the activity of phosphate solubilization is influenced by exogenous soluble phosphate. In the present study, the effects of soluble phosphate on the activity of phosphate solubilization, acidification of media, growth, and organic acid secretion of phosphate-solubilizing bacterium Pseudomonas frederiksbergensis JW-SD2 were investigated under six levels of soluble phosphate conditions. The activity of phosphate solubilization decreased with the increase of soluble phosphate concentration, accompanying with the increase of media pH. However, the growth was promoted by adding soluble phosphate. Production of gluconic, tartaric, and oxalic acids by the strain was reduced with the increase of concentration of soluble phosphate, while acetic and pyruvic acids showed a remarkable increase. Gluconic acid predominantly produced by the strain at low levels of soluble phosphate showed that this acid was the most efficient organic acid in phosphate solubilization. Pyrroloquinoline quinone-glucose dehydrogenase gene gcd (pg5SD2) was cloned from the strain, and the expressions of pg5SD2 gene were repressed gradually with the increase of concentration of soluble phosphate. The soluble phosphate regulating the transcription of the gcd gene is speculated to underlie the regulation of the secretion of gluconic acid and subsequently the regulation of the activity of phosphate solubilization. Future research needs to consider a molecular engineering strategy to reduce the sensitivity of PSB strain to soluble phosphate via modification of the regulatory mechanism of gcd gene, which could improve the scope of PSB strains' application.

  11. Can Phosphate Salts Recovered from Manure Replace Conventional Phosphate Fertilizer?

    Directory of Open Access Journals (Sweden)

    Andrea Ehmann

    2017-01-01

    Full Text Available Pig farming produces more manure than can reasonably be spread onto surrounding fields, particularly in regions with high livestock densities and limited land availability. Nutrient recycling offers an attractive solution for dealing with manure excesses and is one main objective of the European commission-funded project “BioEcoSIM”. Phosphate salts (“P-Salt” were recovered from the separated liquid manure fraction. The solid fraction was dried and carbonized to biochar. This study compared the fertilizing performance of P-Salt and conventional phosphate fertilizer and determined whether additional biochar application further increased biomass yields. The fertilizers and biochar were tested in pot experiments with spring barley and faba beans using two nutrient-poor soils. The crops were fertilized with P-Salt at three levels and biochar in two concentrations. Biomass yield was determined after six weeks. Plant and soil samples were analysed for nitrogen, phosphorus and potassium contents. The P-Salt had similar or even better effects than mineral fertilizer on growth in both crops and soils. Slow release of nutrients can prevent leaching, rendering P-Salt a particularly suitable fertilizer for light sandy soils. Biochar can enhance its fertilizing effect, but the underlying mechanisms need further investigation. These novel products are concluded to be promising candidates for efficient fertilization strategies.

  12. Proton induced luminescence of minerals

    Energy Technology Data Exchange (ETDEWEB)

    Calvo del Castillo, H.; Millan, A.; Calderon, T. [Depto. Geologia y Geoquimica, Universidad Autonoma de Madrid, Ctra. Colmenar, km. 15, 28049, Madrid (Spain); Beneitez, P. [Departamento Quimica Fisica Aplicada, Universidad Autonoma de Madrid Cantoblanco, Madrid (Spain); Ruvalcaba S, J.L. [lFUNAM, Circuito de la lnvestigacion Cientifica s/n, Ciudad Universitaria, 04510 Mexico D.F. (Mexico)

    2008-07-01

    This paper presents a summary of Ionoluminescence (IL) for several minerals commonly found in jewellery pieces and/or artefacts of historical interest. Samples including silicates and non-silicates (native elements, halide, oxide, carbonate and phosphate groups) have been excited with a 1.8 MeV proton beam, and IL spectra in the range of 200- 900 nm have been collected for each one using a fiber optic coupled spectrometer. Light emissions have been related to Cr{sup 3+}, Mn{sup 2+} and Pr{sup 3+} ions, as well as intrinsic defects in these minerals. Results show the potential of IL for impurity characterization with high detection limits, local symmetry studies, and the study of the origin of minerals. (Author)

  13. Aggregate and Mineral Resources - Minerals

    Data.gov (United States)

    NSGIC State | GIS Inventory — This point occurrence data set represents the current mineral and selected energy resources of Utah. The data set coordinates were derived from USGS topographic maps...

  14. Nevadaite, (Cu2+, Al, V3+)6 [Al8 (PO4)8 F8] (OH 2 (H2O)22, a new phosphate mineral species from the Gold Quarry mine, Carlin, Eureka County, Nevada: description and crystal structure

    Science.gov (United States)

    Cooper, M.A.; Hawthorne, F.C.; Roberts, Andrew C.; Foord, E.E.; Erd, Richard C.; Evans, H.T.; Jensen, M.C.

    2004-01-01

    Nevadaite, (Cu2+, ???, Al, V3+)6 (PO4)8 F8 (OH)2 (H2O)22, is a new supergene mineral species from the Gold Quarry mine, near Carlin, Eureka County, Nevada, U.S.A. Nevadaite forms radiating clusters to 1 mm of prismatic crystals, locally covering surfaces more that 2 cm across; individual crystals are elongate on [001] with a length:width ratio of > 10:1 and a maximum diameter of ???30 ??m. It also occurs as spherules and druses associated with colorless to purple-black fluellite, colorless wavellite, strengitevariscite, acicular maroon-to-red hewettite, and rare anatase, kazakhstanite, tinticite, leucophosphite, torbernite and tyuyamunite. Nevadaite is pale green to turquoise blue with a pale powder-blue streak and a vitreous luster; it does not fluoresce under ultra-violet light. It has no cleavage, a Mohs hardness of ???3, is brittle with a conchoidal fracture, and has measured and calculated densities of 2.54 and 2.55 g/cm3, respectively. Nevadaite is biaxial negative, with ?? 1.540, ?? 1.548, ?? 1.553, 2V(obs.) = 76??, 2V(calc.) = 76??, pleochroic with X pale greenish blue, Y very pale greenish blue, Z blue, and with absorption Z ??? X > Y and orientation X = c, Y = a, Z = b. Nevadaite is orthorhombic, space group P21mn, a 12.123(2), b 18.999(2), c 4.961(1) A?? , V 1142.8(2) A??3, Z = 1, a:b:c = 0.6391:1:0.2611. The strongest seven lines in the X-ray powder-diffraction pattern [d in A??(I)(hkl)] are: 6.077(10)(200), 5.618(9)(130), 9.535(8)(020), 2.983(6)(241), 3.430(4)(041), 2.661(4)(061 , and 1.844(4)(352). A chemical analysis with an electron microprobe gave P2O5 32.54, Al2O3 27.07, V2O3 4.24, Fe2O3 0.07, CuO 9.24, ZnO 0.11, F 9.22, H2O (calc.) 23.48, OH ??? F -3.88, sum 102.09 wt.%; the valence states of V and Fe, and the amount of H2O, were determined by crystal-structure analysis. The resulting empirical formula on the basis of 63.65 anions (including 21.65 H2O pfu) is (CU2+2.00 Zn0.02 V3+0.98 Fe3+0.01 Al1.15)??4.16 Al8 P7.90 O32 [F8.37 (OH 1.63]??10 (H2O

  15. Chemical changes of titanium and titanium dioxide under electron bombardment

    OpenAIRE

    Romins Brasca; Luciana Ines Vergara; Mario César Guillermo Passeggi; Julio Ferrón

    2007-01-01

    The electron induced effect on the first stages of the titanium (Ti0) oxidation and titanium dioxide (Ti4+) chemical reduction processes has been studied by means of Auger electron spectroscopy. Using factor analysis we found that both processes are characterized by the appearance of an intermediate Ti oxidation state, Ti2O3 (Ti3+).

  16. Plasmonic Titanium Nitride Nanostructures via Nitridation of Nanopatterned Titanium Dioxide

    DEFF Research Database (Denmark)

    Guler, Urcan; Zemlyanov, Dmitry; Kim, Jongbum

    2017-01-01

    Plasmonic titanium nitride nanostructures are obtained via nitridation of titanium dioxide. Nanoparticles acquired a cubic shape with sharper edges following the rock-salt crystalline structure of TiN. Lattice constant of the resulting TiN nanoparticles matched well with the tabulated data. Energ...

  17. Chemical changes of titanium and titanium dioxide under electron bombardment

    Directory of Open Access Journals (Sweden)

    Romins Brasca

    2007-09-01

    Full Text Available The electron induced effect on the first stages of the titanium (Ti0 oxidation and titanium dioxide (Ti4+ chemical reduction processes has been studied by means of Auger electron spectroscopy. Using factor analysis we found that both processes are characterized by the appearance of an intermediate Ti oxidation state, Ti2O3 (Ti3+.

  18. Corrosion of titanium in phosphoric acid at 250 ℃

    Institute of Scientific and Technical Information of China (English)

    LU Jian-shu

    2009-01-01

    Corrosion studies of a commercially pure titanium in phosphoric acid solutions at 250 ℃ were carried out by immersion test in an autoclave. At lower phosphoric acid concentration (0.1 mol/L), the corrosion was mild. At higher phosphoric concentration (1.0 mol/L) corrosion, a 25 μm-thick white corrosion products layer was formed on the samples after 24 h immersion. XRD analysis shows that the white layer consists mainly of titanium oxide phosphate hydrate (π-Ti2O(PO4)2·2H2O). The corrosion product shows the morphology of fiber bundles. A thermodynamic analysis of the formation of the corrosion product is presented.

  19. Control of vertebrate skeletal mineralization by polyphosphates.

    Directory of Open Access Journals (Sweden)

    Sidney Omelon

    Full Text Available BACKGROUND: Skeletons are formed in a wide variety of shapes, sizes, and compositions of organic and mineral components. Many invertebrate skeletons are constructed from carbonate or silicate minerals, whereas vertebrate skeletons are instead composed of a calcium phosphate mineral known as apatite. No one yet knows why the dynamic vertebrate skeleton, which is continually rebuilt, repaired, and resorbed during growth and normal remodeling, is composed of apatite. Nor is the control of bone and calcifying cartilage mineralization well understood, though it is thought to be associated with phosphate-cleaving proteins. Researchers have assumed that skeletal mineralization is also associated with non-crystalline, calcium- and phosphate-containing electron-dense granules that have been detected in vertebrate skeletal tissue prepared under non-aqueous conditions. Again, however, the role of these granules remains poorly understood. Here, we review bone and growth plate mineralization before showing that polymers of phosphate ions (polyphosphates: (PO(3(-(n are co-located with mineralizing cartilage and resorbing bone. We propose that the electron-dense granules contain polyphosphates, and explain how these polyphosphates may play an important role in apatite biomineralization. PRINCIPAL FINDINGS/METHODOLOGY: The enzymatic formation (condensation and destruction (hydrolytic degradation of polyphosphates offers a simple mechanism for enzymatic control of phosphate accumulation and the relative saturation of apatite. Under circumstances in which apatite mineral formation is undesirable, such as within cartilage tissue or during bone resorption, the production of polyphosphates reduces the free orthophosphate (PO(4(3- concentration while permitting the accumulation of a high total PO(4(3- concentration. Sequestering calcium into amorphous calcium polyphosphate complexes can reduce the concentration of free calcium. The resulting reduction of both free PO

  20. Internal adaptation of cast titanium crowns

    Directory of Open Access Journals (Sweden)

    Sicknan Soares da Rocha

    2007-08-01

    Full Text Available As the adaptation of titanium crowns obtained by Rematitan Plus investment, specific for titanium, is not recognized to be suitable, this study evaluated the effect of the concentration of the specific liquid and the temperature of the mold of investments on the internal misfit of crowns cast on commercially pure titanium. Individual dies of epoxy resin were obtained, representing teeth prepared for full-crown restoration with a 6-degree axial surface convergence angle and shoulder (1.0 mm. For the waxing of each crown, a ring-shaped stainless steel matrix (8.0mm internal diameter; 7.5 mm height was adapted above the individual dies of epoxy resin. The Rematian Plus investment was mixed according to the manufacturer's instructions using two different concentrations of the specific liquid: 100%, 75%. Casting was performed in a Discovery Plasma Ar-arc vacuum-pressure casting machine with molds at temperatures of 430ºC, 515ºC and 600ºC. The crowns were cleaned individually in a solution (1% HF + 13% HNO3 for 10 min using a ultrasonic cleaner, with no internal adaptations, and luted with zinc phosphate cement under a 5 kg static load. The crown and die assemblies were embedded in resin and sectioned longitudinally. The area occupied by cement was observed using stereoscopic lens (10X and measured by the Leica Qwin image analysis system (mm². The data for each experimental condition (n=8 were analyzed by Kruskal-Wallis non-parametric test (á=0.05. The results showed that liquid dilution and the increase in mold temperature did not significantly influence the levels of internal fit of the cast titanium crowns. The lowest means (±SD of internal misfit were obtained for the 430ºC/100%: (7.25 mm² ±1.59 and 600ºC/100% (8.8 mm² ±2.25 groups, which presented statistically similar levels of internal misfit.

  1. Characterization and quantification of oxides generated by anodization on titanium for implantation purposes

    Science.gov (United States)

    Aloia Games, L.; Pastore, J.; Bouchet, A.; Ballarre, J.

    2011-12-01

    The use of titanium as implant material is widely known in the surgery field. The formation of natural or artificial compact and protective oxide is a convenient tool for metal protection and a good way to generate phosphate deposits to enhance biocompatibility and bone fixation with the existing tissue. The present work has the aim of superficially modify commercially pure titanium sheets used in orthopedics and odontology, with a potencistatic anodization process with an ammonium phosphate and ammonium fluoride solution as electrolyte. The objective is to generate titanium oxides doped with phosphorous on the surface, to promote bioactivity. The characterization and quantification of the generated deposits is presented as a starting point for the future application of these materials. The applied characterization methods are X ray diffraction, micro-Raman spectroscopy analysis for evaluating the chemical and phase composition on the modified surface and PDI image analysis techniques that allow the segmentation of SEM images and the measurement and quantification of the oxides generated by the anodization process. The samples with polished treated surface at 30V have the deposit of a phosphate rich thick layer covering almost all the surface and spherical-shaped titanium oxide crystals randomly placed (covering more than 20% of the surface area).

  2. Fumarolic minerals

    DEFF Research Database (Denmark)

    Balic Zunic, Tonci; Garavelli, Anna; Jakobsson, Sveinn Peter

    2016-01-01

    The fumarolic mineralogy of the Icelandic active volcanoes, the Tyrrhenian volcanic belt (Italy) and the Aegean active arc (Greece) is investigated, and literature data surveyed in order to define the characteristics of the European fumarolic systems. They show broad diversity of mineral...... associations, with Vesuvius and Vulcano being also among the world localities richest in mineral species. Volcanic systems, which show recession over a longer period, show fumarolic development from the hightemperature alkaline halide/sulphate, calcic sulphate or sulphidic parageneses, synchronous...... fluctuations in activity, illustrated by the example of Vulcano where the high-temperature association appears intermittently. A full survey of the mineral groups and species is given in respect to their importance and appearance in fumarolic associations....

  3. 30 CFR 46.5 - New miner training.

    Science.gov (United States)

    2010-07-01

    ... RETRAINING OF MINERS ENGAGED IN SHELL DREDGING OR EMPLOYED AT SAND, GRAVEL, SURFACE STONE, SURFACE CLAY, COLLOIDAL PHOSPHATE, OR SURFACE LIMESTONE MINES. § 46.5 New miner training. (a) Except as provided in... the recognition and avoidance of electrical hazards and other hazards present at the mine, such...

  4. Calcium Phosphate Coating over Silk Fibroin Film by Biomimetic Methods

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    To investigate the biomineralization behavior of silk fibroin and to valuate the biodegradation and biocompatibility of the hybrid biomaterial, the calcium phosphate deposits were identified with SEM, EDX,XRD and FTIR. The results reveal that supersaturated calcification solution is an effective method for the mineralization of fibroin film. Enzymatic degradation experiment demonstrates the biodegradability of the composites. Osteoblasts incubation shows an excellent cytocompatibility on the mineralized fibroin films.

  5. Titanium dioxide nanotube films

    Energy Technology Data Exchange (ETDEWEB)

    Roman, Ioan, E-mail: roman@metav-cd.ro [S.C. METAV-Research and Development S.R.L., Bucharest, 31C. A. Rosetti, 020011 (Romania); Trusca, Roxana Doina; Soare, Maria-Laura [S.C. METAV-Research and Development S.R.L., Bucharest, 31C. A. Rosetti, 020011 (Romania); Fratila, Corneliu [Research and Development National Institute for Nonferrous and Rare Metals, Pantelimon, 102 Biruintei, 077145 (Romania); Krasicka-Cydzik, Elzbieta [University of Zielona Gora, Department of Biomedical Engineering Division, 9 Licealna, 65-417 (Poland); Stan, Miruna-Silvia; Dinischiotu, Anca [University of Bucharest, Department of Biochemistry and Molecular Biology, 36-46 Mihail Kogalniceanu, 050107 (Romania)

    2014-04-01

    Titania nanotubes (TNTs) were prepared by anodization on different substrates (titanium, Ti6Al4V and Ti6Al7Nb alloys) in ethylene glycol and glycerol. The influence of the applied potential and processing time on the nanotube diameter and length is analyzed. The as-formed nanotube layers are amorphous but they become crystalline when subjected to subsequent thermal treatment in air at 550 °C; TNT layers grown on titanium and Ti6Al4V alloy substrates consist of anatase and rutile, while those grown on Ti6Al7Nb alloy consist only of anatase. The nanotube layers grown on Ti6Al7Nb alloy are less homogeneous, with supplementary islands of smaller diameter nanotubes, spread across the surface. Better adhesion and proliferation of osteoblasts was found for the nanotubes grown on all three substrates by comparison to an unprocessed titanium plate. The sensitivity towards bovine alkaline phosphatase was investigated mainly by electrochemical impedance spectroscopy in relation to the crystallinity, the diameter and the nature of the anodization electrolyte of the TNT/Ti samples. The measuring capacity of the annealed nanotubes of 50 nm diameter grown in glycerol was demonstrated and the corresponding calibration curve was built for the concentration range of 0.005–0.1 mg/mL. - Highlights: • Titania nanotubes (TNTs) on Ti, Ti6Al4V and Ti6Al7Nb substrates were prepared. • Quantitative dependences of anodization conditions on TNT features were established. • Morphology and electrochemical tests revealed inhomogeneity of TNT/Ti6Al7Nb films. • Particular characteristics of TNT films induce electrochemical sensitivity to ALP. • Annealed TNT/Ti impedimetric sensitivity towards ALP was demonstrated and quantified.

  6. Effect of Phosphate on U(VI) Sorption to Montmorillonite: Ternary Complexation and Precipitation Barriers

    Energy Technology Data Exchange (ETDEWEB)

    Troyer, Lyndsay D.; Maillot, Fabien; Wang, Zheming; Wang, Zimeng; Mehta, Vrajesh; Giammar, Daniel; Catalano, Jeffrey G.

    2016-02-15

    Phosphate addition is a potential treatment method to lower the solubility of U(VI) in soil and groundwater systems by causing U(VI) phosphate precipitation as well as enhancing adsorption. Previous work has shown that iron oxide surfaces may facilitate the nucleation of U(VI) phosphate minerals and, that under weakly acidic conditions, phosphate also enhances U(VI) adsorption to such phases. Like iron oxides, clays are important reactive phases in the subsurface but little is known about the interaction of U(VI) and phosphate with these minerals. The effect of aqueous phosphate on U(VI) binding to Wyoming montmorillonite (SWy-2) in air-equilibrated systems was investigated. Equilibrium U(VI) uptake to montmorillonite was determined at pH 4, 6 and 8 at discrete initial phosphate concentrations between 0 and 100 μM. The observed behavior of U(VI) indicates a transition from adsorption to precipitation with increasing total uranium and phosphate concentrations at all pH values. At the highest phosphate concentration examined at each pH value, a barrier to U(VI) phosphate nucleation is observed. At lower concentrations, phosphate has no effect on macroscopic U(VI) adsorption. To assess the mechanisms of U(VI)-phosphate interactions on smectite surfaces, U(VI) speciation was investigated under selected conditions using laser-induced fluorescence spectroscopy (LIFS) and extended X-ray absorption fine-structure (EXAFS) spectroscopy. Samples above the precipitation threshold display EXAFS and LIFS spectral signatures consistent with the autunite family of U(VI) phosphate minerals. However, at lower U(VI) concentrations, changes in LIFS spectra upon phosphate addition suggest that U(VI)-phosphate ternary surface complexes form on the montmorillonite surface at pH 4 and 6 despite the lack of a macroscopic effect on adsorption. The speciation of solid-associated U(VI) below the precipitation threshold at pH 8 is dominated by U(VI)-carbonate surface complexes. This work

  7. Effect of phosphate on U(VI) sorption to montmorillonite: Ternary complexation and precipitation barriers

    Science.gov (United States)

    Troyer, Lyndsay D.; Maillot, Fabien; Wang, Zheming; Wang, Zimeng; Mehta, Vrajesh S.; Giammar, Daniel E.; Catalano, Jeffrey G.

    2016-02-01

    Phosphate addition is a potential treatment method to lower the solubility of U(VI) in soil and groundwater systems by causing U(VI) phosphate precipitation as well as enhancing adsorption. Previous work has shown that iron oxide surfaces may facilitate the nucleation of U(VI) phosphate minerals and, that under weakly acidic conditions, phosphate also enhances U(VI) adsorption to such phases. Like iron oxides, clays are important reactive phases in the subsurface but little is known about the interaction of U(VI) and phosphate with these minerals. The effect of aqueous phosphate on U(VI) binding to Wyoming montmorillonite (SWy-2) in air-equilibrated systems was investigated. Equilibrium U(VI) uptake to montmorillonite was determined at pH 4, 6 and 8 at discrete initial phosphate concentrations between 0 and 100 μM. The observed behavior of U(VI) indicates a transition from adsorption to precipitation with increasing total uranium and phosphate concentrations at all pH values. At the highest phosphate concentration examined at each pH value, a barrier to U(VI) phosphate nucleation is observed. At lower concentrations, phosphate has no effect on macroscopic U(VI) adsorption. To assess the mechanisms of U(VI)-phosphate interactions on smectite surfaces, U(VI) speciation was investigated under selected conditions using laser-induced fluorescence spectroscopy (LIFS) and extended X-ray absorption fine-structure (EXAFS) spectroscopy. Samples above the precipitation threshold display EXAFS and LIFS spectral signatures consistent with the autunite family of U(VI) phosphate minerals. However, at lower U(VI) concentrations, changes in LIFS spectra upon phosphate addition suggest that U(VI)-phosphate ternary surface complexes form on the montmorillonite surface at pH 4 and 6 despite the lack of a macroscopic effect on adsorption. The speciation of solid-associated U(VI) below the precipitation threshold at pH 8 is dominated by U(VI)-carbonate surface complexes. This work

  8. A study on the potential application of natural phosphate in photocatalytic processes.

    Science.gov (United States)

    Hidalgo-Carrillo, Jesús; Sebti, Jalila; Aramendía, María A; Marinas, Alberto; Marinas, José M; Sebti, Said; Urbano, Francisco J

    2010-04-15

    In an attempt at increasing surface area of the resulting solids, different titanium-based systems were synthesized on natural phosphate through the sol-gel process using diverse ageing conditions (reflux, magnetic stirring, sonication or microwaves) and tested for gas-phase selective photooxidation of propan-2-ol. The best results were obtained for the system aged under ultrasounds which was ascribed to its lower band-gap energy. Moreover, the synthesis of TiO(2) on natural phosphate seemed to produce retardation in crystallization as well as a change in titanium and phosphorus electronic environments (as determined by XPS) which in the case of the sonicated system resulted in an improved catalytic behavior as compared to pure titania. All in all, the present piece of research shows that provided that its surface area can be increased natural phosphate can be used as support for a photocatalytic active phase thus widening the scope of its application.

  9. In vivo evaluation of titanium implants coated with bioactive glass by pulsed laser deposition.

    Science.gov (United States)

    Borrajo, Jacinto P; Serra, Julia; González, Pío; León, Betty; Muñoz, Fernando M; López, M

    2007-12-01

    During the past years, different techniques, like chemical treatment, plasma spraying, sputtering, enamelling or sol-gel; and materials, like metals, hydroxylapatite, calcium phosphates, among others, have been applied in different combinations to improve the performance of prostheses. Among the techniques, Pulsed Laser Deposition (PLD) is very promising to produce coatings of bioactive glass on any metal alloy used as implant. In this work the biocompatibility of PLD coatings deposited on titanium substrates was examined by implantation in vivo. Different coating compositions were checked to find the most bioactive that was then applied on titanium and implanted into paravertebral muscle of rabbit.

  10. Characterization of bioactive ceramic coatings prepared on titanium implants by micro-arc oxidation

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Micro-arc oxidation (MAO) is an enhanced chemical technology in an electrolyte medium to obtain coating structures on valve-metal surfaces. Titanium oxide films obtained by MAO in the sodium phosphate electrolyte were investigated. The films were composed mainly of TiO2 phases in the form of anatase and rutile and enriched with Na and P elements at the surface. Their apatite-inducing ability was evaluated in a simulated body fluid (SBF). When immersing in SBF for over 30 d, a preferential carbonated-hydroxyapatite was formed on the surfaces of the films, which suggests that the MAO-treated titanium has a promising positive biological response.

  11. Characterization and protein-adsorption behavior of deposited organic thin film onto titanium by plasma polymerization with hexamethyldisiloxane.

    Science.gov (United States)

    Hayakawa, Tohru; Yoshinari, Masao; Nemoto, Kimiya

    2004-01-01

    Plasma polymerized hexamethyldisiloxane (HMDSO) thin film was deposited onto titanium using a radio-frequency apparatus for the surface modification of titanium. A titanium disk was first polished using colloidal silica at pH=9.8. Plasma-polymerized HMDSO films were firmly attached to the titanium by heating the titanium to a temperature of approximately 250 degrees C. The thickness of the deposited film was 0.07-0.35mum after 10-60min of plasma polymerization. The contact angle with respect to double distilled water significantly increased after HMDSO coating. X-ray photoelectron spectroscopy revealed that the deposited thin film consisted of Si, C, and O atoms. No Ti peaks were observed on the deposited surface. The deposited HMDSO film was stable during 2-weeks immersion in phosphate buffer saline solution. Fourier transform reflection-absorption spectroscopy showed the formation of Si-H, Si-C, C-H, and Cz.dbnd6;O bonds in addition to Si-O-Si bonds. Quartz crystal microbalance-dissipation measurement demonstrated that the deposition of HMDSO thin films on titanium has a benefit for fibronectin adsorption at the early stage. In conclusion, plasma polymerization is a promising technique for the surface modification of titanium. HMDSO-coated titanium has potential application as a dental implant material.

  12. Effect of titanium addition on thermal stability of hydroxyapatite/zirconia nanocomposite

    Directory of Open Access Journals (Sweden)

    Wang L.I.

    2015-01-01

    Full Text Available HA/ZrO2 composite nanpowder with various addition of titanium (0.2-2.4wt% were synthesized via wet chemical method using ZrOCl2.8H2O, H3PO4, Ca(OH2 and tetraethylorthotitanate as precursor materials. The composites were then sintered at 900-1200ºC for 2h, respectively. Effect of titanium addition to the composite on the phase composition and thermal stability during thermal treatment was investigated. The results suggested that as the sintering temperature increased from 900°C to 1200ºC and with the addition of titanium to the composite below 0.8wt%, main phases were HA and ZrO2. As the sintering temperature increased to 1200°C and with the addition of titanium to the composite above 0.8wt%, main phases were HA, ZrO2 and a small amount of dicalcium phosphate (DCP. There were still no tricalcium phosphate (β-TCP and CaZrO3 phases observed, which indicated that the addition of titanium restrained decomposition of HA and thermal reaction between HA and ZrO2. It also suggested that the addition of 0.8wt% titanium to the composite was optimum for producing HA/ZrO2 composite nanopowder with expected main phases. With the addition of 0.8wt% titanium to the composite, SEM images showed that the individual particles of the two materials were still visible, which also implied that the reaction between HA and ZrO2 did not occur.

  13. Engineering Titanium for Improved Biological Response

    Energy Technology Data Exchange (ETDEWEB)

    Orme, C; Bearinger, J; Dimasi, E; Gilbert, J

    2002-01-23

    The human body and its aggressive environment challenge the survival of implanted foreign materials. Formidable biocompatibility issues arise from biological, chemical, electrical, and tribological origins. The body's electrolytic solution provides the first point of contact with any kind of implant, and is responsible for transport, healing, integration, or attack. Therefore, determining how to successfully control the integration of a biomaterial should begin with an analysis of the early interfacial dynamics involved. setting, a complicated feedback system of solution chemistry, pH, ions, and solubility exists. The introduction of a fixation device instantly confounds this system. The body is exposed to a range of voltages, and wear can bring about significant shifts in potentials across an implant. In the environment of a new implant the solution pH becomes acidic, ionic concentrations shift, cathodic currents can lead to corrosion, and oxygen levels can be depleted; all of these impact the ability of the implant to retain its protective oxide layer and to present a stable interface for the formation of a biolayer. Titanium has been used in orthopedic and maxilofacial surgery for many years due to its reputation as being biocompatible and its ability to osseointegrate. Osseointegration is defined as direct structural and functional connection between ordered, living bone, and the surface of a load carrying implant. Branemark discovered this phenomenon in the 60's while examining titanium juxtaposed to bone. The mechanism by which titanium and its passivating oxide encourage osseosynthetic activity remains unknown. However in general terms the oxide film serves two purposes: first to provide a kinetic barrier that prevents titanium from corroding and second to provide a substrate that allows the constituents of bone (calcium phosphate crystals, cells, proteins, and collagen) to bond to it. We believe that the electrochemical environment dictates the

  14. Mineral resource of the month: zirconium and hafnium

    Science.gov (United States)

    Gambogi, Joseph

    2007-01-01

    Zirconium and hafnium are corrosion-resistant metals that are grouped in the same family as titanium on the periodic table. The two elements commonly occur in oxide and silicate minerals and have significant economic importance in everything from ink, ceramics and golf shoes to nuclear fuel rods.

  15. Compaction of Titanium Powders

    Energy Technology Data Exchange (ETDEWEB)

    Gerdemann, Stephen,J; Jablonski, Paul, J

    2011-05-01

    Accurate modeling of powder densification has been an area of active research for more than 60 years. The earliest efforts were focused on linearization of the data because computers were not readily available to assist with curve-fitting methods. In this work, eight different titanium powders (three different sizes of sponge fines<150 {micro}m,<75 {micro}m, and<45 {micro}m; two different sizes of a hydride-dehydride [HDH]<75 {micro}m and<45 {micro}m; an atomized powder; a commercially pure [CP] Ti powder from International Titanium Powder [ITP]; and a Ti 6 4 alloy powder) were cold pressed in a single-acting die instrumented to collect stress and deformation data during compaction. From these data, the density of each compact was calculated and then plotted as a function of pressure. The results show that densification of all the powders, regardless of particle size, shape, or chemistry, can be modeled accurately as the sum of an initial density plus the sum of a rearrangement term and a work-hardening term. These last two terms are found to be a function of applied pressure and take the form of an exponential rise.

  16. Sodium-dependent phosphate transporters in osteoclast differentiation and function.

    Directory of Open Access Journals (Sweden)

    Giuseppe Albano

    Full Text Available Osteoclasts are multinucleated bone degrading cells. Phosphate is an important constituent of mineralized bone and released in significant quantities during bone resorption. Molecular contributors to phosphate transport during the resorptive activity of osteoclasts have been controversially discussed. This study aimed at deciphering the role of sodium-dependent phosphate transporters during osteoclast differentiation and bone resorption. Our studies reveal RANKL-induced differential expression of sodium-dependent phosphate transport protein IIa (NaPi-IIa transcript and protein during osteoclast development, but no expression of the closely related NaPi-IIb and NaPi-IIc SLC34 family isoforms. In vitro studies employing NaPi-IIa-deficient osteoclast precursors and mature osteoclasts reveal that NaPi-IIa is dispensable for bone resorption and osteoclast differentiation. These results are supported by the analysis of structural bone parameters by high-resolution microcomputed tomography that yielded no differences between adult NaPi-IIa WT and KO mice. By contrast, both type III sodium-dependent phosphate transporters Pit-1 and Pit-2 were abundantly expressed throughout osteoclast differentiation, indicating that they are the relevant sodium-dependent phosphate transporters in osteoclasts and osteoclast precursors. We conclude that phosphate transporters of the SLC34 family have no role in osteoclast differentiation and function and propose that Pit-dependent phosphate transport could be pivotal for bone resorption and should be addressed in further studies.

  17. Effect of pH and coexisting anions on removal of phosphate from aqueous solutions by inorganic-based mesostructures.

    Science.gov (United States)

    Choi, Jae-Woo; Choi, Yong-Soo; Hong, Seok-Won; Kim, Dong-Ju; Lee, Sang-Hyup

    2012-07-01

    This study investigated the effect of pH and the presence of coexisting (competitive) anions on the removal of phosphate by titanium mesostructures synthesized using do- or hexadecyltrimethylammonium bromide. To address these research objectives, experiments were conducted (1) under controlled initial pH values (2 to 10); and (2) through injection of nitrate, fluoride, chloride, or sulfate anions into a phosphate solution. Based on the experimental results, an initial of pH of 2 was found to be optimal for use of titanium mesostructures. The presence of fluoride anions in solution significantly decreased the removal efficiency of phosphate removal (3.56% at 3.95 mg/g). However, the addition of nitrate, chloride, and sulfate anions did not affect phosphate removal.

  18. Is Struvite a Prebiotic Mineral?

    Directory of Open Access Journals (Sweden)

    Matthew A. Pasek

    2013-04-01

    Full Text Available The prebiotic relevance of mineral struvite, MgNH4PO4·6H2O, was studied experimentally as a phosphorylating reagent and, theoretically, to understand the geochemical requirements for its formation. The effectiveness of phosphorylation by the phosphate mineral, monetite, CaHPO4, was also studied to compare to the efficiency of struvite. The experiments focused on the phosphorylation reactions of the minerals with organic compounds, such as nucleosides, glycerol and choline chloride, and heat at 75 °C for about 7–8 days and showed up to 28% phosphorylation of glycerol. In contrast, the compositional requirements for the precipitation of struvite are high ammonium and phosphate concentrations, as well as a little Ca2+ dissolved in the water. Combined, these requirements suggest that it is not likely that struvite was present in excess on the early Earth to carry out phosphorylation reactions. The present study focuses on the thermodynamic aspects of struvite formation, complementing the results given by Orgel and Handschuh (1973, which were based on the kinetic effects.

  19. Is Struvite a Prebiotic Mineral?

    Science.gov (United States)

    Gull, Maheen; Pasek, Matthew A.

    2013-01-01

    The prebiotic relevance of mineral struvite, MgNH4PO4·6H2O, was studied experimentally as a phosphorylating reagent and, theoretically, to understand the geochemical requirements for its formation. The effectiveness of phosphorylation by the phosphate mineral, monetite, CaHPO4, was also studied to compare to the efficiency of struvite. The experiments focused on the phosphorylation reactions of the minerals with organic compounds, such as nucleosides, glycerol and choline chloride, and heat at 75 °C for about 7–8 days and showed up to 28% phosphorylation of glycerol. In contrast, the compositional requirements for the precipitation of struvite are high ammonium and phosphate concentrations, as well as a little Ca2+ dissolved in the water. Combined, these requirements suggest that it is not likely that struvite was present in excess on the early Earth to carry out phosphorylation reactions. The present study focuses on the thermodynamic aspects of struvite formation, complementing the results given by Orgel and Handschuh (1973), which were based on the kinetic effects. PMID:25369744

  20. Mineralogy, textures, and whole-rock geochemistry of advanced argillic alteration: Hugo Dummett porphyry Cu-Au deposit, Oyu Tolgoi mineral district, Mongolia

    Science.gov (United States)

    Khashgerel, Bat-Erdene; Kavalieris, Imants; Hayashi, Ken-Ichiro

    2008-11-01

    Advanced argillic (AA) alteration is developed over a vertical interval of 500 m, above (and enclosing) Late Devonian quartz monzodiorite intrusions that accompany porphyry-style Cu-Au mineralization at the Hugo Dummett deposit. The AA alteration is mainly in basaltic rocks and locally extends into the overlying dacitic ash-flow tuff for about 100 m. The AA zone overprints porphyry-style quartz veins associated with quartz monzodiorite intrusions, but at least partly precedes high-grade porphyry-style bornite mineralization. Mineralogically, it consists of andalusite, corundum, residual quartz, titanium oxides, diaspore, alunite, aluminum phosphate-sulfate (APS) minerals, zunyite, pyrophyllite, topaz, kaolinite, and dickite, as well as anhydrite and gypsum, but is dominated by residual quartz and pyrophyllite. Alteration zonation is not apparent, except for an alunite-bearing zone that occurs approximately at the limit of strong quartz veining. Whole-rock geochemistry shows that the AA alteration removes most major elements except Si, Al, Ti, and P, and removes the trace elements Sc, Cs, and Rb. V, Zr, Hf, Nb, Ta, U, and Th are relatively immobile, whilst light REEs (La to Nd), Sr, Ba, and Ga can be enriched. Middle REEs (Sm to Gd) are moderately depleted; Y and heavy REEs (Tb to Lu) are strongly depleted except in two unusual samples where middle to heavy REEs are enriched.

  1. Effect of various laser irradiations on the mineral content of dentin.

    Science.gov (United States)

    Dilber, Erhan; Malkoc, Meral Arslan; Ozturk, A Nilgun; Ozturk, Firat

    2013-01-01

    THE AIM OF THIS STUDY WAS TO EVALUATE THE MINERAL CONTENT OF DENTIN IRRADIATION WITH ERBIUM: yttrium-aliminum-garnet (Er:YAG), Neodmiyum:yttrium-aliminum garnet (Nd:YAG) and potassium titanium phosphate (KTP) laser used for in the treatment of dentin hypersensitivity. Six extracted wisdom, unerupted molar teeth were used in this study. The enamel of the teeth was removed with a conventional bur under water cooling to expose the dentin surface. The teeth were mounted in a slow-speed, diamond-saw, sectioning machine. Two dentin slabs were obtained from each tooth and each slab was sectioned so that 4 slabs were made from each teeth. Then dentin slabs were randomly divided into four groups. Group A: Control Group, Group B: Er:YAG laser, Group C: Nd:YAG laser, Group D: KTP laser. The levels of Ca, K, Mg, Na,P and Ca/P mineral ratio in each dentin slab were measured by inductively coupled plasma-atomic emission spectrometry (ICP-AES). Data were analysed by one way analysis of variance (ANOVA) and Tukey HSD tests. One sample from each group was prepared for scanning electron microscopy (SEM). There were no significant differences between the groups for Ca, K, Mg, Na,P and Ca/P mineral ratio (P>.05). SEM photographs indicated that there were melted areas around the exposed dentin tubules in groups treated with Er:YAG and KTP lasers. This study demonstrated that laser etching with the Er:YAG, Nd:YAG, KTP laser systems did not affect the compositional structure of the dentin surfaces.

  2. Amorphous calcium phosphate and its application in dentistry

    Directory of Open Access Journals (Sweden)

    Sun Wei-bin

    2011-07-01

    Full Text Available Abstract Amorphous Calcium Phosphate (ACP is an essential mineral phase formed in mineralized tissues and the first commercial product as artificial hydroxyapatite. ACP is unique among all forms of calcium phosphates in that it lacks long-range, periodic atomic scale order of crystalline calcium phosphates. The X-ray diffraction pattern is broad and diffuse with a maximum at 25 degree 2 theta, and no other different features compared with well-crystallized hydroxyapatite. Under electron microscopy, its morphological form is shown as small spheroidal particles in the scale of tenths nanometer. In aqueous media, ACP is easily transformed into crystalline phases such as octacalcium phosphate and apatite due to the growing of microcrystalline. It has been demonstrated that ACP has better osteoconductivity and biodegradability than tricalcium phosphate and hydroxyapatite in vivo. Moreover, it can increase alkaline phosphatase activities of mesoblasts, enhance cell proliferation and promote cell adhesion. The unique role of ACP during the formation of mineralized tissues makes it a promising candidate material for tissue repair and regeneration. ACP may also be a potential remineralizing agent in dental applications. Recently developed ACP-filled bioactive composites are believed to be effective anti-demineralizing/remineralizing agents for the preservation and repair of tooth structures. This review provides an overview of the development, structure, chemical composition, morphological characterization, phase transformation and biomedical application of ACP in dentistry.

  3. Metal-phosphate binders

    Science.gov (United States)

    Howe, Beth Ann [Lewistown, IL; Chaps-Cabrera, Jesus Guadalupe [Coahuila, MX

    2009-05-12

    A metal-phosphate binder is provided. The binder may include an aqueous phosphoric acid solution, a metal-cation donor including a metal other than aluminum, an aluminum-cation donor, and a non-carbohydrate electron donor.

  4. Osseointegration of titanium implants in the tibia. Electron microscopy of biopsies from 4 patients.

    Science.gov (United States)

    Serre, C M; Boivin, G; Obrant, K J; Linder, L

    1994-06-01

    We studied the ultrastructure of bone tissue around implants of pure titanium inserted into the tibia in 4 patients with arthrosis or rheumatoid arthritis. Three main appearances of the interface were noted. First, a close contact between titanium and calcified bone with living osteocytes inside the newly-formed bone was observed in all samples. Secondly, a close contact was also seen between the implant and osteoid, the newly formed collagenous matrix being either uncalcified or calcifying. Thirdly, a loose extracellular matrix with fibrillar and nonfibrillar materials was sometimes observed between bone mineral and implant. There was no inflammatory reaction at the interface. We concluded that the titanium implants were osseointegrated, but the calcification of the bone tissue was not complete even after 20 months. However, mineralization of osteoid and living bone cells revealed the presence of an active tissue.

  5. Osteogenesis around CaP-coated titanium implants visualized using 3D histology and micro-computed tomography

    NARCIS (Netherlands)

    Cuijpers, V.M.J.I.; Alghamdi, H.S.; Dijk, N.W.M. van; Jaroszewicz, J.; Walboomers, X.F.; Jansen, J.A.

    2015-01-01

    Calcium phosphate (CaP) coatings can enhance the performance of bone implants in compromised conditions, such as osteoporosis. Therefore, this study compared non-coated vs. CaP-coated (n = 8) titanium implants in osteoporotic ovariectomized (OVX) rats. Bone volume (BV) was assessed using micro-compu

  6. Purification and utilization of titanium

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Wonbaek; Yu, Hyosin; Chung, Inwha; Rhee, Kang In; Choi, Good Sun; Lee, Chulkyung; Youn, In Ju; Chung, Jinki; Suh, Chang Youl; Yang, Dong Hyo [Korea Institute of Geology Mining and Materials, Taejon (Korea, Republic of)

    1997-12-01

    Current domestic market appears not to be sufficient enough for the large scale investment for the expensive vacuum-melting equipment. Besides, related ingot-processing technologies like rolling, extrusion, and forging of titanium should be prepared in advance. In the mean time, the attempt to recycle expensive titanium scraps produced in our nation would be worthwhile in view of the reduction of import from foreign countries and of saving valuable secondary resources. The objectives for this research is to develop technology for the production of high purity titanium metals from sponges and scraps and to extend the developed technology to industrial applications. PREP(Plasma-Rotating-Electrode Process) and HDP(Hydride-Dehydride Process) were adopted to evaluate the possibility of using domestic titanium scraps in the production of pure titanium powders. Those scraps were titanium pipes of Grade 2 and various sputtering targets having a purity of 99.995%. The titanium powders produced by both methods were examined and compared with conventionally prepared ones. Their shape, size distribution, structure and above of all major impurities were determine to evaluate these process. The powders produced by PREP were of round shape having narrow size distribution at about 200 micron. Meanwhile, HDP powders were irregular shaped having a much wider size distribution. Both metallic and non-metallic impurities were lower in PREP powders due to the unavoidable contamination during crushing processes in HDP. Thus, PREP has advantages towards purity and uniformity while HDP toward finer sizes. Apparently, for the production of high purity titanium powders by HDP, special considerations should be made to prevent contamination during various steps in the process. In PREP powders, smaller particles contained more oxygen since they have larger surface/volume ratio. The tendency was also observed in the hardness measurement revealing the strengthening effect of oxygen in pure

  7. Mineralization by nanobacteria

    Science.gov (United States)

    Kajander, E. Olavi; Bjorklund, Michael; Ciftcioglu, Neva

    1998-07-01

    Nanobacteria are the smallest cell-walled bacteria, only recently discovered in human and cow blood and in commercial cell culture serum. In this study, we identified with energy-dispersive x-ray microanalysis and chemical analysis that all growth phases of nanobacteria produce biogenic apatite on their cell envelope. Fourier transform IR spectroscopy revealed the mineral as carbonate apatite. Previous models for stone formation have lead to a hypothesis that an elevated pH due to urease and/or alkaline phosphatase activity are important lithogenic factors. Our results indicate that carbonate apatite can be formed without these factors at pH 7.4 at physiological phosphate and calcium concentrations. Due to their specific macromolecules, nanobacteria can produce apatite very efficiency in media mimicking tissue fluids and glomerular filtrate and rapidly mineralizing most of available calcium and phosphate. This can be also monitored by (superscript 85)Sr incorporation and provides a unique model for in vitro studies on calcification. Recently, bacteria have been implicated in the formation of carbonate (hydroxy)fluorapatite in marine sediments. Apatite grains are found so commonly in sedimentary rocks that apatite is omitted in naming the stone. To prove that apatite and other minerals are formed by bacteria would implicate that the bacteria could be observed and their actions followed in stones. We have started to approach this in two ways. Firstly, by the use of sensitive methods for detecting specific bacterial components, like antigens, muramic acid and nucleic acids, that allow for detecting the presence of bacteria and, secondly, by follow-up of volatile bacterial metabolites observed by continuous monitoring with ion mobility spectrometry, IMCELL, working like an artificial, educatable smelling nose. The latter method might allow for remote real time detection of bacterial metabolism, a signature of life, in rocks via fractures of drillholes with or without

  8. Characteristics productive and meat quality of broiler chickens fed finisher diet without vitamin-mineral supplement or limestone and dicalcium phosphate and submitted to heat stress pre-slaughter Características produtivas e de qualidade de carne de frangos de corte submetidos a dietas de terminação sem suplemento vitamínicomineral ou calcário e fosfato bicálcico e submetidos a estresse térmico pré-abate

    Directory of Open Access Journals (Sweden)

    Sandra Regina Brunelli

    2012-02-01

    Full Text Available Search mechanisms that can reduce the cost of production of poultry is an important factor in the poultry industry. Thus the objective of this study was to evaluate the removal of vitamin and mineral supplement or limestone and dicalcium phosphate feed during the finishing phase, further of the broilers chickens to heat stress pre-slaughter. Hybro male broiler (n=108 aged 42 days old were evaluated until 49 days old to evaluate the performance, carcass and cuts yield, blood biochemistry and meat quality. The results showed that the removal of vitamin and mineral supplement or limestone and dicalcium phosphate feed during the finishing phase did not impair the performance, carcass characteristics and meat quality, as well as showing a possible mechanism to reduce production costs. While heat stress pre-slaughter provided a poor meat quality of poultry. Buscar mecanismos que possam reduzir o custo de produção das aves, sem reduzir o desempenho e a qualidade do produto final é um importante fator dentro da cadeia avícola. Desta forma, o objetivo deste trabalho foi avaliar a retirada do suplemento vitamínico-mineral ou calcário e fosfato bicálcico da ração na fase de acabamento, além de submeter os frangos de corte a estresse térmico pré-abate visando avaliar o desempenho e a qualidade de carne do peito. Foram utilizados 108 frangos de corte machos da linhagem Hybro com 42 dias de idade, que receberam uma ração controle, ração sem suplemento vitamínico-mineral e sem calcário e fosfato bicálcico, dos 42 aos 49 dias de idade. Foram avaliados os dados de desempenho, rendimento de carcaça e cortes, bioquímica do sangue e qualidade de carne. Os resultados mostraram que a retirada do suplemento vitamínico-mineral ou o calcário e o fosfato bicálcico da dieta de terminação não prejudicou o desempenho, características de carcaça e qualidade de carne, mostrando assim como um possível mecanismo para reduzir os custos de produ

  9. Recent revisions of phosphate rock reserves and resources: a critique

    NARCIS (Netherlands)

    Edixhoven, J.D.; Gupta, J.; Savenije, H.H.G.

    2014-01-01

    Phosphate rock (PR) is a finite mineral indispensable for fertilizer production, while P (phosphorus) is a major pollutant if applied or discharged in excess, causing widespread eutrophication (Carpenter and Bennet, 2011). High-grade PR is obtained from deposits which took millions of years to form

  10. Recent revisions of phosphate rock reserves and resources: a critique

    NARCIS (Netherlands)

    Edixhoven, J.D.; Gupta, J.; Savenije, H.H.G.

    2014-01-01

    Phosphate rock (PR) is a finite mineral indispensable for fertilizer production, while P (phosphorus) is a major pollutant if applied or discharged in excess, causing widespread eutrophication (Carpenter and Bennet, 2011). High-grade PR is obtained from deposits which took millions of years to form

  11. Mineral bioprocessing

    Energy Technology Data Exchange (ETDEWEB)

    Torma, A.E.

    1993-05-01

    In the last 25 years, the introduction of biotechnological methods in hydrometallurgy has created new opportunities and challenges for the mineral processing industry. This was especially true for the production of metal values from mining wastes and low-and-complex-grade mineral resources, which were considered economically not amenable for processing by conventional extraction methods. Using bio-assisted heap, dump and in-situ leaching technologies, copper and uranium extractions gained their first industrial applications. The precious metal industries were the next to adopt the bio-preoxidation technique in the extraction of gold from refractory sulfide-bearing ores and concentrates. A variety of other bioleaching opportunities exist for nickel, cobalt, cadmium and zinc sulfide leaching. Recently developed bioremediation methods and biosorption technologies have shown a good potential for industrial applications to remove trace heavy metal and radionuclide concentrations from contaminated soils, and mining and processing effluents.

  12. Antimicrobial titanium/silver PVD coatings on titanium

    OpenAIRE

    Thull Roger; Glückermann Susanne K; Ewald Andrea; Gbureck Uwe

    2006-01-01

    Abstract Background Biofilm formation and deep infection of endoprostheses is a recurrent complication in implant surgery. Post-operative infections may be overcome by adjusting antimicrobial properties of the implant surface prior to implantation. In this work we described the development of an antimicrobial titanium/silver hard coating via the physical vapor deposition (PVD) process. Methods Coatings with a thickness of approximately 2 μm were deposited on titanium surfaces by simultaneous ...

  13. Plasma electrolytic oxidation of Titanium Aluminides

    Science.gov (United States)

    Morgenstern, R.; Sieber, M.; Grund, T.; Lampke, T.; Wielage, B.

    2016-03-01

    Due to their outstanding specific mechanical and high-temperature properties, titanium aluminides exhibit a high potential for lightweight components exposed to high temperatures. However, their application is limited through their low wear resistance and the increasing high-temperature oxidation starting from about 750 °C. By the use of oxide ceramic coatings, these constraints can be set aside and the possible applications of titanium aluminides can be extended. The plasma electrolytic oxidation (PEO) represents a process for the generation of oxide ceramic conversion coatings with high thickness. The current work aims at the clarification of different electrolyte components’ influences on the oxide layer evolution on alloy TNM-B1 (Ti43.5Al4Nb1Mo0.1B) and the creation of compact and wear resistant coatings. Model experiments were applied using a ramp-wise increase of the anodic potential in order to show the influence of electrolyte components on the discharge initiation and the early stage of the oxide layer growth. The production of PEO layers with technically relevant thicknesses close to 100 μm was conducted in alkaline electrolytes with varying amounts of Na2SiO3·5H2O and K4P2O7 under symmetrically pulsed current conditions. Coating properties were evaluated with regard to morphology, chemical composition, hardness and wear resistance. The addition of phosphates and silicates leads to an increasing substrate passivation and the growth of compact oxide layers with higher thicknesses. Optimal electrolyte compositions for maximum coating hardness and thickness were identified by statistical analysis. Under these conditions, a homogeneous inner layer with low porosity can be achieved. The frictional wear behavior of the compact coating layer is superior to a hard anodized layer on aluminum.

  14. Infrared spectroscopy of different phosphates structures.

    Science.gov (United States)

    Jastrzębski, W; Sitarz, M; Rokita, M; Bułat, K

    2011-08-15

    Infrared (IR) spectroscopic studies of mineral and synthetic phosphates have been presented. The interpretation of the spectra has been preceded by the isolated [PO(4)](3-) tetrahedron spectra analyse. The K(3)PO(4) saturated aqueous solution was measured in the special cell for liquids. The obtained IR results have been compared with the theoretical number of IR-active modes. The number and positions of the bands due to P-O vibrations have been established. The phase composition of the phosphates has been determined using XRD and IR spectroscopy methods. The influence of non-tetrahedral cations on the shape of the spectra and the positions of bands has been analysed and the crystalline field splitting effect has been discussed.

  15. Odontoblast phosphate and calcium transport in dentinogenesis.

    Science.gov (United States)

    Lundquist, Patrik

    2002-01-01

    It has been suggested that odontoblasts are instrumental in translocating Ca2+ and inorganic phosphate (Pi) ions during the mineralization of dentin. The aim of this thesis was, therefore, to study the expression of components of the transcellular ion transport system, Na+/Ca2+ exchangers and Na(+)-Pi contransporters, in odontoblastic and osteoblastic cells. Their activity was assayed in osteoblast-like cells and in the recently developed MRPC-1 odontoblast-like cell line. To assess the relationship between ion transport and mineralization, Ca2+ and Pi uptake activities were determined in mineralizing cultures of MRPC-1 cells. Osteoblastic and odontoblastic cells showed an identical expression pattern of Na+/Ca2+ exchanger splice-variants, NCX1.3, NCX1.7 and NCX1.10, derived from the NCX1 gene, while NCX2 was not expressed. The cells showed a high sodium-dependent calcium extrusion activity. Regarding Na(+)-Pi cotransporter expression, Glvr-1, Ram-1 and the two high capacity cotransporters Npt-2a and Npt-2b were found to be expressed in odontoblasts and MRPC-1 cells. Osteoblast-like cells differed from this in expressing the Npt-1 but not the Ram-1 gene but were otherwise identical to the odontoblastic cells. Odontoblast-like cells exhibited almost twice the sodium-dependent Pi uptake activity of osteoblast-like cells. The presence of NaPi-2a and NaPi-2b, gene products of Npt-2a and Npt-2b, was verified in vivo by immunohistochemistry on mouse teeth. Both cotransporters could be detected in fully differentiated, polarized odontoblasts but not in preodontoblasts prior to dentin formation. Both cotransporters were detected in adjacent bone and in ameloblasts. Studying ion uptake in mineralizing MRPC-1 cultures, large changes were detected concomitant with the onset of mineral formation, when phosphate uptake increased by 400% while calcium uptake started to decline. The increase in Pi uptake was found to be due to activation of the NaPi-2a cotransporter. MRPC-1 cells

  16. Advanced titanium processing

    Energy Technology Data Exchange (ETDEWEB)

    Hartman, Alan D.; Gerdemann, Stephen J.; Schrems, Karol K.; Holcomb, Gordon R.; Argetsinger, Edward R.; Hansen, Jeffrey S.; Paige, Jack I.; Turner, Paul C.

    2001-01-01

    The Albany Research Center of the U.S. Department of Energy has been investigating a means to form useful wrought products by direct and continuous casting of titanium bars using cold-wall induction melting rather than current batch practices such as vacuum arc remelting. Continuous ingots produced by cold-wall induction melting, utilizing a bottomless water-cooled copper crucible, without slag (CaF2) additions had minor defects in the surface such as ''hot tears''. Slag additions as low as 0.5 weight percent were used to improve the surface finish. Therefore, a slag melted experimental Ti-6Al-4V alloy ingot was compared to a commercial Ti-6Al-4V alloy ingot in the areas of physical, chemical, mechanical, and corrosion attributes to address the question, ''Are any detrimental effects caused by slag addition''?

  17. Hemocompatibility of titanium nitride.

    Science.gov (United States)

    Dion, I; Baquey, C; Candelon, B; Monties, J R

    1992-10-01

    The left ventricular assist device is based on the principle of the Maillard-Wenkel rotative pump. The materials which make up the pump must present particular mechanical, tribological, thermal and chemical properties. Titanium nitride (TiN) because of its surface properties and graphite because of its bulk characteristics have been chosen. The present study evaluated the in vitro hemocompatibility of TiN coating deposited by the chemical vapor deposition process. Protein adsorption, platelet retention and hemolysis tests have been carried out. In spite of some disparities, the TiN behavior towards albumin and fibrinogen is interesting, compared with the one of a reference medical grade elastomer. The platelet retention test gives similar results as those achieved with the same elastomer. The hemolysis percentage is near to zero. TiN shows interesting characteristics, as far as mechanical and tribological problems are concerned, and presents very encouraging blood tolerability properties.

  18. Sorption of phosphate onto calcite; results from batch experiments and surface complexation modeling

    DEFF Research Database (Denmark)

    Sø, Helle Ugilt; Postma, Dieke; Jakobsen, Rasmus;

    2011-01-01

    The adsorption of phosphate onto calcite was studied in a series of batch experiments. To avoid the precipitation of phosphate-containing minerals the experiments were conducted using a short reaction time (3h) and low concentrations of phosphate (⩽50μM). Sorption of phosphate on calcite...... was studied in 11 different calcite-equilibrated solutions that varied in pH, PCO2, ionic strength and activity of Ca2+, CO32- and HCO3-. Our results show strong sorption of phosphate onto calcite. The kinetics of phosphate sorption onto calcite are fast; adsorption is complete within 2–3h while desorption...... of a high degree of super-saturation with respect to hydroxyapatite (SIHAP⩽7.83). The amount of phosphate adsorbed varied with the solution composition, in particular, adsorption increases as the CO32- activity decreases (at constant pH) and as pH increases (at constant CO32- activity). The primary effect...

  19. Electrochemical process of titanium extraction

    Institute of Scientific and Technical Information of China (English)

    CH. RVS. NAGESH; C. S. RAMACHANDRAN

    2007-01-01

    A wide variety of processes are being pursued by researchers for cost effective extraction of titanium metal. Electrochemical processes are promising due to simplicity and being less capital intensive. Some of the promising electrochemical processes of titanium extraction were reviewed and the results of laboratory scale experiments on electrochemical reduction of TiO2 granules were brought out. Some of the kinetic parameters of the reduction process were discussed while presenting the quality improvements achieved in the experimentation.

  20. Enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium

    Directory of Open Access Journals (Sweden)

    Zhu W

    2015-12-01

    Full Text Available Wei Zhu,1 George Teel,1 Christopher M O’Brien,1 Taisen Zhuang,1 Michael Keidar,1 Lijie Grace Zhang1–3 1Department of Mechanical and Aerospace Engineering, 2Department of Biomedical Engineering, 3Department of Medicine, The George Washington University, Washington, DC, USA Abstract: Surface modification of titanium for use in orthopedics has been explored for years; however, an ideal method of integrating titanium with native bone is still required to this day. Since human bone cells directly interact with nanostructured extracellular matrices, one of the most promising methods of improving titanium’s osseointegration involves inducing biomimetic nanotopography to enhance cell–implant interaction. In this regard, we explored an approach to functionalize the surface of titanium by depositing a thin film of textured titanium nanoparticles via a cathodic arc discharge plasma. The aim is to improve human bone marrow mesenchymal stem cell (MSC attachment and differentiation and to reduce deleterious effects of more complex surface modification methods. Surface functionalization was analyzed by scanning electron microscopy, atomic force microscopy, contact angle testing, and specific protein adsorption. Scanning electron microscopy and atomic force microscopy examination demonstrate the deposition of titanium nanoparticles and the surface roughness change after coating. The specific fibronectin adsorption was enhanced on the modified titanium surface that associates with the improved hydrophilicity. MSC adhesion and proliferation were significantly promoted on the nanocoated surface. More importantly, compared to bare titanium, greater production of total protein, deposition of calcium mineral, and synthesis of alkaline phosphatase were observed from MSCs on nanocoated titanium after 21 days. The method described herein presents a promising alternative method for inducing more cell favorable nanosurface for improved orthopedic applications

  1. Detonation nanodiamonds biofunctionalization and immobilization to titanium alloy surfaces as first steps towards medical application.

    Science.gov (United States)

    Gonçalves, Juliana P L; Shaikh, Afnan Q; Reitzig, Manuela; Kovalenko, Daria A; Michael, Jan; Beutner, René; Cuniberti, Gianaurelio; Scharnweber, Dieter; Opitz, Jörg

    2014-01-01

    Due to their outstanding properties nanodiamonds are a promising nanoscale material in various applications such as microelectronics, polishing, optical monitoring, medicine and biotechnology. Beyond the typical diamond characteristics like extreme hardness or high thermal conductivity, they have additional benefits as intrinsic fluorescence due to lattice defects without photobleaching, obtained during the high pressure high temperature process. Further the carbon surface and its various functional groups in consequence of the synthesis, facilitate additional chemical and biological modification. In this work we present our recent results on chemical modification of the nanodiamond surface with phosphate groups and their electrochemically assisted immobilization on titanium-based materials to increase adhesion at biomaterial surfaces. The starting material is detonation nanodiamond, which exhibits a heterogeneous surface due to the functional groups resulting from the nitrogen-rich explosives and the subsequent purification steps after detonation synthesis. Nanodiamond surfaces are chemically homogenized before proceeding with further functionalization. Suspensions of resulting surface-modified nanodiamonds are applied to the titanium alloy surfaces and the nanodiamonds subsequently fixed by electrochemical immobilization. Titanium and its alloys have been widely used in bone and dental implants for being a metal that is biocompatible with body tissues and able to bind with adjacent bone during healing. In order to improve titanium material properties towards biomedical applications the authors aim to increase adhesion to bone material by incorporating nanodiamonds into the implant surface, namely the anodically grown titanium dioxide layer. Differently functionalized nanodiamonds are characterized by infrared spectroscopy and the modified titanium alloys surfaces by scanning and transmission electron microscopy. The process described shows an adsorption and

  2. Detonation nanodiamonds biofunctionalization and immobilization to titanium alloy surfaces as first steps towards medical application

    Directory of Open Access Journals (Sweden)

    Juliana P. L. Gonçalves

    2014-11-01

    Full Text Available Due to their outstanding properties nanodiamonds are a promising nanoscale material in various applications such as microelectronics, polishing, optical monitoring, medicine and biotechnology. Beyond the typical diamond characteristics like extreme hardness or high thermal conductivity, they have additional benefits as intrinsic fluorescence due to lattice defects without photobleaching, obtained during the high pressure high temperature process. Further the carbon surface and its various functional groups in consequence of the synthesis, facilitate additional chemical and biological modification. In this work we present our recent results on chemical modification of the nanodiamond surface with phosphate groups and their electrochemically assisted immobilization on titanium-based materials to increase adhesion at biomaterial surfaces. The starting material is detonation nanodiamond, which exhibits a heterogeneous surface due to the functional groups resulting from the nitrogen-rich explosives and the subsequent purification steps after detonation synthesis. Nanodiamond surfaces are chemically homogenized before proceeding with further functionalization. Suspensions of resulting surface-modified nanodiamonds are applied to the titanium alloy surfaces and the nanodiamonds subsequently fixed by electrochemical immobilization. Titanium and its alloys have been widely used in bone and dental implants for being a metal that is biocompatible with body tissues and able to bind with adjacent bone during healing. In order to improve titanium material properties towards biomedical applications the authors aim to increase adhesion to bone material by incorporating nanodiamonds into the implant surface, namely the anodically grown titanium dioxide layer. Differently functionalized nanodiamonds are characterized by infrared spectroscopy and the modified titanium alloys surfaces by scanning and transmission electron microscopy. The process described shows an

  3. Preparation of biocompatible structural gradient coatings on pure titanium

    Institute of Scientific and Technical Information of China (English)

    TANG Guang-xin; ZHANG Ren-ji; YAN Yong-nian

    2004-01-01

    In order to overcome the poor osteo-inductive properties of titanium implant, some methods have been used. The efforts to improve implant biocompatibility and durability by applying a hybrid technique of composite oxidation (pre-anodic and micro-arc oxidation) and hydrothermal treatment were described. Pure titanium was used as the substrate material. An oxalic acid was used as the electrolyte for the pre-anodic oxidation. A calcium and phosphate salt solution was acted as the electrolyte of micro-arc oxidation and the common pure water was used for hydrothermal treatment. X-ray diffraction (XRD), and scanning electron microscopy (SEM) have been used to investigate the microstructure and morphology of the coatings. The results show that a compact TiO2 film can be made by pre-anodic oxidation, which is effective as chemical barriers against the in-vivo release of metal ions from the implants. A porous TiO2 coating can be produced by micro-arc oxidation on titanium plate, which is beneficial to bone tissue growth and enhancing anchorage of implant to bone. De-calcium HA can be formed on the coating using hydrothermal treatment, which is similar with the primary component of bone and has a very good osteo-inductivity.The porous gradient titania coating made by the hybrid oxidation and hydrothermal treatment should show good biocompatibility in the environment of the human body.

  4. Anodisation Increases Integration of Unloaded Titanium Implants in Sheep Mandible

    Directory of Open Access Journals (Sweden)

    Warwick J. Duncan

    2015-01-01

    Full Text Available Spark discharge anodic oxidation forms porous TiO2 films on titanium implant surfaces. This increases surface roughness and concentration of calcium and phosphate ions and may enhance early osseointegration. To test this, forty 3.75 mm × 13 mm titanium implants (Megagen, Korea were placed into healed mandibular postextraction ridges of 10 sheep. There were 10 implants per group: RBM surface (control, RBM + anodised, RBM + anodised + fluoride, and titanium alloy + anodised surface. Resonant frequency analysis (RFA was measured in implant stability quotient (ISQ at surgery and at sacrifice after 1-month unloaded healing. Mean bone-implant contact (% BIC was measured in undemineralised ground sections for the best three consecutive threads. One of 40 implants showed evidence of failure. RFA differed between groups at surgery but not after 1 month. RFA values increased nonsignificantly for all implants after 1 month, except for controls. There was a marked difference in BIC after 1-month healing, with higher values for alloy implants, followed by anodised + fluoride and anodised implants. Anodisation increased early osseointegration of rough-surfaced implants by 50–80%. RFA testing lacked sufficient resolution to detect this improvement. Whether this gain in early bone-implant contact is clinically significant is the subject of future experiments.

  5. Titanium in the geothermal industry

    Energy Technology Data Exchange (ETDEWEB)

    Thomas, R. [TIMET UK Ltd., Swansea (United Kingdom)

    2003-12-01

    Titanium resists seawater and brine at temperatures as high as 260{sup o}C, and is also resistant to corrosion by sulphur dioxide; hydrogen sulphide; and aqueous solutions of those gases. Titanium is fully resistant to corrosion and stress corrosion cracking in the standard NACE test solution containing 3000 ppm dissolved H{sub 2}S, 5% NACl, and 0.5% acetic acid (pH 3.5). To avoid pitting at temperatures above 80{sup o}C, titanium alloys containing nickel, molybdenum, palladium or ruthenium are used. Examples of equipment fabricated in titanium in order to withstand the corrosive fluids present in some geothermal installations are plate heat exchangers and well casing. By careful selection of the grade of titanium, material thickness (with no corrosion allowance) and fabrication method, an economic fabrication with low maintenance costs and high availability can be achieved. A prime example of the application of titanium in the geothermal industry is the use of Grade 29 well casing in the Salton Sea, USA, which enables the exploitation of a geothermal resource containing highly corrosive brine. Advances in production technology are being applied to reduce the cost of the casing pipe. This technology may enable the use of sea water injection to augment weak or depleted aquifers, or to generate steam from Hot Dry Rocks. (author)

  6. Hydrothermal minerals

    Digital Repository Service at National Institute of Oceanography (India)

    Nath, B.N.

    -floor hydrothermal processes involving free circulation of seawater through ocean crust as convection. Heat flow, seafloor fracturing, permeability and fluid composition are the parameters governing the type and extent of mineralization. The chimney like... stream_size 23365 stream_content_type text/plain stream_name Refresher_Course_Mar_Geol_Geophys_2007_Lecture_Notes_78.pdf.txt stream_source_info Refresher_Course_Mar_Geol_Geophys_2007_Lecture_Notes_78.pdf.txt Content-Encoding UTF-8...

  7. Hybrid calcium phosphate coatings for implants

    Science.gov (United States)

    Malchikhina, Alena I.; Shesterikov, Evgeny V.; Bolbasov, Evgeny N.; Ignatov, Viktor P.; Tverdokhlebov, Sergei I.

    2016-08-01

    Monophasic biomaterials cannot provide all the necessary functions of bones or other calcined tissues. It is necessary to create for cancer patients the multiphase materials with the structure and composition simulating the natural bone. Such materials are classified as hybrid, obtained by a combination of chemically different components. The paper presents the physical, chemical and biological studies of coatings produced by hybrid technologies (HT), which combine primer layer and calcium phosphate (CaP) coating. The first HT type combines the method of vacuum arc titanium primer layer deposition on a stainless steel substrate with the following micro-arc oxidation (MAO) in phosphoric acid solution with addition of calcium compounds to achieve high supersaturated state. MAO CaP coatings feature high porosity (2-8%, pore size 5-7 µm) and surface morphology with the thickness greater than 5 µm. The thickness of Ti primer layer is 5-40 µm. Amorphous MAO CaP coating micro-hardness was measured at maximum normal load Fmax = 300 mN. It was 3.1 ± 0.8 GPa, surface layer elasticity modulus E = 110 ± 20 GPa, roughness Ra = 0.9 ± 0.1 µm, Rz = 7.5 ± 0.2 µm, which is less than the titanium primer layer roughness. Hybrid MAO CaP coating is biocompatible, able to form calcium phosphates from supersaturated body fluid (SBF) solution and also stimulates osteoinduction processes. The second HT type includes the oxide layer formation by thermal oxidation and then CaP target radio frequency magnetron sputtering (RFMS). Oxide-RFMS CaP coating is a thin dense coating with good adhesion to the substrate material, which can be used for metal implants. The RFMS CaP coating has thickness 1.6 ± 0.1 µm and consists of main target elements calcium and phosphorus and Ca/P ratio 2.4. The second HT type can form calcium phosphates from SBF solution. In vivo study shows that hybrid RFMS CaP coating is biocompatible and produces fibrointegration processes.

  8. Diversity of Phosphate-Dissolving Microorganisms in Corn Rhizosphere

    Institute of Scientific and Technical Information of China (English)

    ZHAO Xiao-rong; LIN Qi-mei; LI Bao-guo

    2003-01-01

    Rhizosphere and nonrhizopshere soils were sampled during corn growth. Total, inorganic phosphate-dissolving and lecithin-mineralizing bacteria, fungi and actinomyctes were determined by plate counting method. Generally, the rhizosphere soil contained around 5 to 100 times more of these bacteria and fungi than the non-rhizosphere soil. However, the actinomycetes in the rhizosphere soil were significantly lower than those in the non-rhizosphere soil. The numbers of these microorganisms didnt significantly change during corn growth in the soils. However, the proportion of the phosphate-dissolving microorganisms in the total changed markedly during corn growth. Generally there were much higher percentages of phosphate-dissolving bacteria and phosphate-dissolving fungi in the rhizosphere soil than the nonrhizosphere soil. More than 90% of the fungi in rhizosphere dissolved inorganic phosphate at the seedling period, but this proportion declined to 20 %at the harvesting time. The community of phosphate-dissolving microorganisms also changed during corn growth. Bacillus was dominant in the nonrhizosphere soil. However, in the rhizosphere, Pseudomonas and Enterobacter became predominant. Penicillium and Streptomyces were the main fungi and actinomycetes capable of dissolving phosphate.

  9. Final Report: Dominant Mechanisms of Uranium-Phosphate Reactions in Subsurface Sediments

    Energy Technology Data Exchange (ETDEWEB)

    Catalano, Jeffrey G. [Washington Univ., St. Louis, MO (United States); Giammar, Daniel E. [Washington Univ., St. Louis, MO (United States); Wang, Zheming [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2016-03-08

    Phosphate addition is an in situ remediation approach that may enhance the sequestration of uranium without requiring sustained reducing conditions. However, the geochemical factors that determine the dominant immobilization mechanisms upon phosphate addition are insufficiently understood to design efficient remediation strategies or accurately predict U(VI) transport. The overall objective of our project is to determine the dominant mechanisms of U(VI)-phosphate reactions in subsurface environments. Our research approach seeks to determine the U(VI)-phosphate solid that form in the presence of different groundwater cations, characterize the effects of phosphate on U(VI) adsorption and precipitation on smectite and iron oxide minerals, examples of two major reactive mineral phases in contaminated sediments, and investigate how phosphate affects U(VI) speciation and fate during water flow through sediments from contaminated sites. The research activities conducted for this project have generated a series of major findings. U(VI) phosphate solids from the autunite mineral family are the sole phases to form during precipitation, with uranyl orthophosphate not occurring despite its predicted greater stability. Calcium phosphates may take up substantial quantities of U(VI) through three different removal processes (adsorption, coprecipitation, and precipitation) but the dominance of each process varies with the pathway of reaction. Phosphate co-adsorbs with U(VI) onto smectite mineral surfaces, forming a mixed uranium-phosphate surface complex over a wide range of conditions. However, this molecular-scale association of uranium and phosphate has not effect on the overall extent of uptake. In contrast, phosphate enhanced U(VI) adsorption to iron oxide minerals at acidic pH conditions but suppresses such adsorption at neutral and alkaline pH, despite forming mixed uranium-phosphate surface complexes during adsorption. Nucleation barriers exist that inhibit U(VI) phosphate

  10. Bone mineralisation in premature infants cannot be predicted from serum alkaline phosphatase or serum phosphate

    DEFF Research Database (Denmark)

    Faerk, J; Peitersen, Birgit; Petersen, S

    2002-01-01

    BACKGROUND: The bone mineral content of premature infants at term is lower than in mature infants at the same postconceptional age. Serum alkaline phosphatase and serum phosphate are often used as indicators of bone mineralisation. OBJECTIVE: To analyse the association between bone mineral content...... and serum alkaline phosphatase and serum phosphate. METHODS: Serum alkaline phosphatase and phosphate were measured at weekly intervals during admission in 108 premature infants of gestational age below 32 weeks (mean (SD) gestational age 29 (2) weeks; mean (SD) birth weight 1129 (279) g). Bone mineral...... content was measured at term (mean gestational age 41 weeks) by dual energy x ray absorptiometry and corrected for body size. RESULTS: Serum alkaline phosphatase was significantly negatively associated with serum phosphate (p serum alkaline...

  11. Phosphate Mines, Jordan

    Science.gov (United States)

    2008-01-01

    Jordan's leading industry and export commodities are phosphate and potash, ranked in the top three in the world. These are used to make fertilizer. The Jordan Phosphate Mines Company is the sole producer, having started operations in 1935. In addition to mining activities, the company produces phosphoric acid (for fertilizers, detergents, pharmaceuticals), diammonium phosphate (for fertilizer), sulphuric acid (many uses), and aluminum fluoride (a catalyst to make aluminum and magnesium). The image covers an area of 27.5 x 49.4 km, was acquired on September 17, 2005, and is located near 30.8 degrees north latitude, 36.1 degrees east longitude. The U.S. science team is located at NASA's Jet Propulsion Laboratory, Pasadena, Calif. The Terra mission is part of NASA's Science Mission Directorate.

  12. Oxidation of o-xylene on mesoporous Ti-phosphate-supported VOx catalysts and promoter effect of K+ on selectivity

    NARCIS (Netherlands)

    Mérida-Robles, J.; Rodríguez-Castellón, E.; Jiménez-López, A.; López Granados, M.; Val, S. del; Melián Cabrera, I.; Fierro, J.L.G.; Jimenez, J

    2005-01-01

    The selective oxidation of o-xylene on catalysts based on mesoporous titanium phosphate-supported vanadium oxide has been studied. The catalysts were characterized by different physico-chemical techniques (XRD, XPS, N-2 isotherms, TPD of chemisorbed NH3 and Raman spectroscopy). The conversion and yi

  13. Cell response of anodized nanotubes on titanium and titanium alloys.

    Science.gov (United States)

    Minagar, Sepideh; Wang, James; Berndt, Christopher C; Ivanova, Elena P; Wen, Cuie

    2013-09-01

    Titanium and titanium alloy implants that have been demonstrated to be more biocompatible than other metallic implant materials, such as Co-Cr alloys and stainless steels, must also be accepted by bone cells, bonding with and growing on them to prevent loosening. Highly ordered nanoporous arrays of titanium dioxide that form on titanium surface by anodic oxidation are receiving increasing research interest due to their effectiveness in promoting osseointegration. The response of bone cells to implant materials depends on the topography, physicochemistry, mechanics, and electronics of the implant surface and this influences cell behavior, such as adhesion, proliferation, shape, migration, survival, and differentiation; for example the existing anions on the surface of a titanium implant make it negative and this affects the interaction with negative fibronectin (FN). Although optimal nanosize of reproducible titania nanotubes has not been reported due to different protocols used in studies, cell response was more sensitive to titania nanotubes with nanometer diameter and interspace. By annealing, amorphous TiO2 nanotubes change to a crystalline form and become more hydrophilic, resulting in an encouraging effect on cell behavior. The crystalline size and thickness of the bone-like apatite that forms on the titania nanotubes after implantation are also affected by the diameter and shape. This review describes how changes in nanotube morphologies, such as the tube diameter, the thickness of the nanotube layer, and the crystalline structure, influence the response of cells.

  14. Silicon-Doped Titanium Dioxide Nanotubes Promoted Bone Formation on Titanium Implants.

    Science.gov (United States)

    Zhao, Xijiang; Wang, Tao; Qian, Shi; Liu, Xuanyong; Sun, Junying; Li, Bin

    2016-02-26

    While titanium (Ti) implants have been extensively used in orthopaedic and dental applications, the intrinsic bioinertness of untreated Ti surface usually results in insufficient osseointegration irrespective of the excellent biocompatibility and mechanical properties of it. In this study, we prepared surface modified Ti substrates in which silicon (Si) was doped into the titanium dioxide (TiO₂) nanotubes on Ti surface using plasma immersion ion implantation (PIII) technology. Compared to TiO₂ nanotubes and Ti alone, Si-doped TiO₂ nanotubes significantly enhanced the expression of genes related to osteogenic differentiation, including Col-I, ALP, Runx2, OCN, and OPN, in mouse pre-osteoblastic MC3T3-E1 cells and deposition of mineral matrix. In vivo, the pull-out mechanical tests after two weeks of implantation in rat femur showed that Si-doped TiO₂ nanotubes improved implant fixation strength by 18% and 54% compared to TiO₂-NT and Ti implants, respectively. Together, findings from this study indicate that Si-doped TiO₂ nanotubes promoted the osteogenic differentiation of osteoblastic cells and improved bone-Ti integration. Therefore, they may have considerable potential for the bioactive surface modification of Ti implants.

  15. Bioactivity of calcium phosphate bioceramic coating fabricated by laser cladding

    Science.gov (United States)

    Zhu, Yizhi; Liu, Qibin; Xu, Peng; Li, Long; Jiang, Haibing; Bai, Yang

    2016-05-01

    There were always strong expectations for suitable biomaterials used for bone regeneration. In this study, to improve the biocompatiblity of titanium alloy, calcium phosphate bioceramic coating was obtained by laser cladding technology. The microstructure, phases, bioactivity, cell differentiation, morphology and resorption lacunae were investigated by optical microscope (OM), x-ray diffraction (XRD), methyl thiazolyl tetrazolium (MTT) assay, tartrate-resistant acid phosphatase (TRAP) staining and scanning electronic microscope (SEM), respectively. The results show that bioceramic coating consists of three layers, which are a substrate, an alloyed layer and a ceramic layer. Bioactive phases of β-tricalcium phosphate (β-TCP) and hydroxyapatite (HA) were found in ceramic coating. Osteoclast precursors have excellent proliferation on the bioceramic surface. The bioceramics coating could be digested by osteoclasts, which led to the resorption lacunae formed on its surface. It revealed that the gradient bioceramic coating has an excellent bioactivity.

  16. Apatite deposition on titanium surfaces--the role of albumin adsorption.

    Science.gov (United States)

    Serro, A P; Fernandes, A C; Saramago, B; Lima, J; Barbosa, M A

    1997-07-01

    Titanium implant surfaces are known to spontaneously nucleate apatite layers when in contact with simulated body fluids. However, adsorption of proteins may influence the process of apatite layer formation. In this study the role of bovine serum albumin (BSA) adsorption in the process of apatite deposition on titanium substrates is investigated. Deposition of calcium phosphate was induced by immersing titanium substrates in a Hank's balanced salt solution (HBSS) for times ranging from 1 to 23 days. The resulting substrates were studied by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), wettability measurements and electrochemical impedance determinations. All these methods indicate the presence of a calcium phosphate layer. The same procedure was repeated substituting HBSS with a solution of BSA in HBSS. Although SEM, EDS and electrochemical impedance spectra do not reveal the presence of an apatite layer, XPS analysis strongly indicates that the inhibition of apatite formation by BSA is only partial. The competition between BSA adsorption and apatite deposition seems to lead to a mixed film where the protein co-exists with calcium phosphate. Wettability studies suggest that this surface film is heterogeneous and porous, similar to the thicker films formed in albumin-free HBSS.

  17. Titanium nanostructures for biomedical applications

    Science.gov (United States)

    Kulkarni, M.; Mazare, A.; Gongadze, E.; Perutkova, Š.; Kralj-Iglič, V.; Milošev, I.; Schmuki, P.; Iglič, A.; Mozetič, M.

    2015-02-01

    Titanium and titanium alloys exhibit a unique combination of strength and biocompatibility, which enables their use in medical applications and accounts for their extensive use as implant materials in the last 50 years. Currently, a large amount of research is being carried out in order to determine the optimal surface topography for use in bioapplications, and thus the emphasis is on nanotechnology for biomedical applications. It was recently shown that titanium implants with rough surface topography and free energy increase osteoblast adhesion, maturation and subsequent bone formation. Furthermore, the adhesion of different cell lines to the surface of titanium implants is influenced by the surface characteristics of titanium; namely topography, charge distribution and chemistry. The present review article focuses on the specific nanotopography of titanium, i.e. titanium dioxide (TiO2) nanotubes, using a simple electrochemical anodisation method of the metallic substrate and other processes such as the hydrothermal or sol-gel template. One key advantage of using TiO2 nanotubes in cell interactions is based on the fact that TiO2 nanotube morphology is correlated with cell adhesion, spreading, growth and differentiation of mesenchymal stem cells, which were shown to be maximally induced on smaller diameter nanotubes (15 nm), but hindered on larger diameter (100 nm) tubes, leading to cell death and apoptosis. Research has supported the significance of nanotopography (TiO2 nanotube diameter) in cell adhesion and cell growth, and suggests that the mechanics of focal adhesion formation are similar among different cell types. As such, the present review will focus on perhaps the most spectacular and surprising one-dimensional structures and their unique biomedical applications for increased osseointegration, protein interaction and antibacterial properties.

  18. The ferroxidase center is essential for ferritin iron loading in the presence of phosphate and minimizes side reactions that form Fe(III)-phosphate colloids.

    Science.gov (United States)

    Hilton, Robert J; David Andros, N; Watt, Richard K

    2012-04-01

    Ferritin iron loading was studied in the presence of physiological serum phosphate concentrations (1 mM), elevated serum concentrations (2-5 mM), and intracellular phosphate concentrations (10 mM). Experiments compared iron loading into homopolymers of H and L ferritin with horse spleen ferritin. Prior to studying the reactions with ferritin, a series of control reactions were performed to study the solution chemistry of Fe(2+) and phosphate. In the absence of ferritin, phosphate catalyzed Fe(2+) oxidation and formed soluble polymeric Fe(III)-phosphate complexes. The Fe(III)-phosphate complexes were characterized by electron microscopy and atomic force microscopy, which revealed spherical nanoparticles with diameters of 10-20 nm. The soluble Fe(III)-phosphate complexes also formed as competing reactions during iron loading into ferritin. Elemental analysis on ferritin samples separated from the Fe(III)-phosphate complexes showed that as the phosphate concentration increased, the iron loading into horse ferritin decreased. The composition of the mineral that does form inside horse ferritin has a higher iron/phosphate ratio (~1:1) than ferritin purified from tissue (~10:1). Phosphate significantly inhibited iron loading into L ferritin, due to the lack of the ferroxidase center in this homopolymer. Spectrophotometric assays of iron loading into H ferritin showed identical iron loading curves in the presence of phosphate, indicating that the ferroxidase center of H ferritin efficiently competes with phosphate for the binding and oxidation of Fe(2+). Additional studies demonstrated that H ferritin ferroxidase activity could be used to oxidize Fe(2+) and facilitate the transfer of the Fe(3+) into apo transferrin in the presence of phosphate.

  19. Surface Modification of Porous Titanium Granules for Improving Bioactivity.

    Science.gov (United States)

    Karaji, Zahra Gorgin; Houshmand, Behzad; Faghihi, Shahab

    The highly porous titanium granules are currently being used as bone substitute material and for bone tissue augmentation. However, they suffer from weak bone bonding ability. The aim of this study was to create a nanostructured surface oxide layer on irregularly shaped titanium granules to improve their bioactivity. This could be achieved using optimized electrochemical anodic oxidation (anodizing) and heat treatment processes. The anodizing process was done in an ethylene glycol-based electrolyte at an optimized condition of 60 V for 3 hours. The anodized granules were subsequently annealed at 450°C for 1 hour. Scanning electron microscopy (SEM), energy-dispersive x-ray spectroscopy (EDS), and x-ray diffraction (XRD) were used to characterize the surface structure and morphology of the granules. The in vitro bioactivity of the samples was evaluated by immersion of specimens in simulated body fluid (SBF) for 1, 2, and 3 weeks. The human osteoblastic sarcoma cell line, MG63, was used to evaluate cell viability on the samples using dimethylthiazol-diphenyl tetrazolium bromide (MTT) assay. The results demonstrated the formation of amorphous nanostructured titanium oxide after anodizing, which transformed to crystalline anatase and rutile phases upon heat treatment. After immersion in SBF, spherical aggregates of amorphous calcium phosphate were formed on the surface of the anodized sample, which turned into crystalline hydroxyapatite on the surface of the anodized annealed sample. No cytotoxicity was detected among the samples. It is suggested that anodic oxidation followed by heat treatment could be used as an effective surface treatment procedure to improve bioactivity of titanium granules implemented for bone tissue repair and augmentation.

  20. A comparative study of zirconium and titanium implants in rat: osseointegration and bone material quality.

    Science.gov (United States)

    Hoerth, Rebecca M; Katunar, María R; Gomez Sanchez, Andrea; Orellano, Juan C; Ceré, Silvia M; Wagermaier, Wolfgang; Ballarre, Josefina

    2014-02-01

    Permanent metal implants are widely used in human medical treatments and orthopedics, for example as hip joint replacements. They are commonly made of titanium alloys and beyond the optimization of this established material, it is also essential to explore alternative implant materials in view of improved osseointegration. The aim of our study was to characterize the implant performance of zirconium in comparison to titanium implants. Zirconium implants have been characterized in a previous study concerning material properties and surface characteristics in vitro, such as oxide layer thickness and surface roughness. In the present study, we compare bone material quality around zirconium and titanium implants in terms of osseointegration and therefore characterized bone material properties in a rat model using a multi-method approach. We used light and electron microscopy, micro Raman spectroscopy, micro X-ray fluorescence and X-ray scattering techniques to investigate the osseointegration in terms of compositional and structural properties of the newly formed bone. Regarding the mineralization level, the mineral composition, and the alignment and order of the mineral particles, our results show that the maturity of the newly formed bone after 8 weeks of implantation is already very high. In conclusion, the bone material quality obtained for zirconium implants is at least as good as for titanium. It seems that the zirconium implants can be a good candidate for using as permanent metal prosthesis for orthopedic treatments.

  1. Transient precursor strategy in mineral formation of bone.

    Science.gov (United States)

    Weiner, Steve

    2006-09-01

    The strategy in biomineralization of initially depositing a less ordered mineral and then transforming it into a more crystalline mature phase is probably widespread among invertebrates. The report in this issue by N.J. Crane, V. Popescu, M.D. Morris, P. Steenhuis, M.A. Ignelzi, Raman spectroscopic evidence for octacalcium phosphate and other mineral species deposited during intramembraneous mineralization. Bone (In press), using micro-Raman spectroscopy to study early mineral deposits in mice calvaria, provides strong evidence that the transient precursor strategy also occurs in vertebrates.

  2. Plasma quench production of titanium from titanium tetrachloride

    Energy Technology Data Exchange (ETDEWEB)

    Sears, J.W.

    1994-10-01

    This project, Plasma Quench Production of Titanium from Titanium Tetrachloride, centers on developing a technique for rapidly quenching the high temperature metal species and preventing back reactions with the halide. The quenching technique chosen uses the temperature drop produced in a converging/diverging supersonic nozzle. The rapid quench provided by this nozzle prevents the back reaction of the halide and metal. The nature of the process produces nanosized particles (10 to 100 nm). The powders are collected by cyclone separators, the hydrogen flared, and the acid scrubbed. Aluminum and titanium powders have been produced in the laboratory-scale device at 1 gram per hour. Efforts to date to scale up this process have not been successful.

  3. Plasmonic titanium nitride nanostructures for perfect absorbers

    DEFF Research Database (Denmark)

    Guler, Urcan; Li, Wen-Wei; Kinsey, Nathaniel

    2013-01-01

    We propose a metamaterial based perfect absorber in the visible region, and investigate the performance of titanium nitride as an alternative plasmonic material. Numerical and experimental results reveal that titanium nitride performs better than gold as a plasmonic absorbing material...

  4. Anticorrosive Performance of Zinc Phosphate Coatings on Mild Steel Developed Using Galvanic Coupling

    Directory of Open Access Journals (Sweden)

    M. Arthanareeswari

    2013-01-01

    Full Text Available The anticorrosive performance of zinc phosphate coatings developed by galvanic coupling technique on mild steel substrates using the cathode materials such as titanium (Ti, copper (Cu, brass (BR, nickel (Ni, and stainless steel (SS is elucidated in this study. Thermal and chemical stability tests, immersion test in 3.5% NaCl, ARE salt droplet test, and salt spray test were carried out. The study reveals that the mild steel substrates phosphated under galvanically coupled condition showed better corrosion resistance than the one coated without coupling. The open circuit potential (OCP of phosphated mild steel panels in 3.5% NaCl was found to be a function of phosphate coating weight and porosity of the coating.

  5. Results of bone regenerate study after osteosynthesis with bioinert and calcium phosphate-coated bioactive implants in experimental femoral neck fractures (experimental study

    Directory of Open Access Journals (Sweden)

    K. S. Kazanin

    2015-01-01

    Full Text Available Objective - to analyze the results of X-ray, cytomorphometric and immunohistochemistry experimental studies of bone regenerates after osteosynthesis with bioinert and calcium phosphate-coated bioactive implants. Material and methods. The study was conducted on experimental femoral neck fractures in rabbit males. Reparative osteogenesis processes were studied in groups of bioinert titanium implant osteosynthesis and calcium phosphate-coated bioactive titanium implant osteosynthesis. The animals were clinically followed-up during the postoperative period. X-ray, cytomorphometric and immunohistochemistry studies of samples extracted from femoral bones were conducted over time on days 1, 7, 14, 30 and 60. The animal experiments were kept and treated according to recommendations of international standards, Helsinki Declaration on animal welfare and approved by the local ethics committee. All surgeries were performed under anesthesia, and all efforts were made to minimize the suffering of the animals. Results. In the animal group without femoral neck fracture osteosynthesis, femoral neck pseudoarthrosis was observed at the end of the experiment. The results of cytomorphometric and immunohistochemistry studies conducted on day 60 of the experiment confirmed that the cellular composition of the bone regenerate in the group of calcium phosphate-coated bioactive titanium implants corresponded to a more mature bone tissue than in the group of bioinert titanium implants. Conclusion. The results of the statistical analysis of cytomorphometric and immunohistochemistry data show that the use of calcium phosphate-coated bioactive titanium implants allows to achieve significantly earlier bone tissue regeneration.

  6. Research on Uncrystallized Phosphating Film

    Institute of Scientific and Technical Information of China (English)

    TANG En-jun; XING Ze-kuan

    2004-01-01

    This article excogitated a kind of uncrystallized phosphating film bears wearing capacity goodly by adding Ca2 + in normal phosphating solution. This technology is very useful to protect steel parts working in oil from abrasion.

  7. Glucose-6-phosphate dehydrogenase deficiency

    Science.gov (United States)

    ... medlineplus.gov/ency/article/000528.htm Glucose-6-phosphate dehydrogenase deficiency To use the sharing features on this page, please enable JavaScript. Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a condition in which ...

  8. Lightweight Protective Coatings For Titanium Alloys

    Science.gov (United States)

    Wiedemann, Karl E.; Taylor, Patrick J.; Clark, Ronald K.

    1992-01-01

    Lightweight coating developed to protect titanium and titanium aluminide alloys and titanium-matrix composite materials from attack by environment when used at high temperatures. Applied by sol-gel methods, and thickness less than 5 micrometers. Reaction-barrier and self-healing diffusion-barrier layers combine to protect titanium alloy against chemical attack by oxygen and nitrogen at high temperatures with very promising results. Can be extended to protection of other environmentally sensitive materials.

  9. Anodic growth of titanium dioxide nanostructures

    DEFF Research Database (Denmark)

    2010-01-01

    Disclosed is a method of producing nanostructures of titanium dioxide (TiO 2 ) by anodisation of titanium (Ti) in an electrochemical cell, comprising the steps of: immersing a non-conducting substrate coated with a layer of titanium, defined as the anode, in an electrolyte solution...... an electrical contact to the layer of titanium on the anode, where the electrical contact is made in the electrolyte solution...

  10. THE EFFICACY OF USING PHOSPHATE SOLUBILIZING MICROORGANISMS IN GRANULAR BIOFERTILIZERS WITH PHOSPHATE ORE

    Directory of Open Access Journals (Sweden)

    Dunaitsev I. A.

    2016-03-01

    Full Text Available Two granular formulations of phosphorus biofertilizers combining rock phosphate and two highly active phosphate solubilizing strains: Acinetobacter species 305 and Pseudomonas species 181а have been investigated. Granules of about 3 mm in size were obtained by contact-convective drying of a mixture of ground ore, concentrated biomass of two different strains, starch and glucose. Micro granules with size of 0.1- 0.5 mm were obtained by spray drying the biomass of two different strains and application of dried cells on the particles of the ground ore. Starch was used as a binder. In the model liquid medium it was shown that the microorganisms have retained the ability to solubilize mineral phosphates in granular formulations prepared. In laboratory pot trial on marigold (Tagetes patula it was demonstrated that both formulations of biofertilizer increased the dry weight of the plants to the same level as that of chemical fertilizer - double superphosphate, but were inferior in the concentration of phosphorus in plants. Both formulations exceeded the effectiveness of rock phosphate and biomass used as biofertilizers both separately and jointly. No significant differences were noted between the two strains and the two granular formulations both for plant dry weight, and the content of phosphorus therein. Both granular formulations of biofertilizer retained their structure and avoided aggregating over a year of storage at 4 oC. The average persistence of living cells in the microbeads was about 1.5%, in granules - 32 %

  11. Shear bond strength between titanium alloys and composite resin: sandblasting versus fluoride-gel treatment.

    Science.gov (United States)

    Lim, Bum-Soon; Heo, Seok-Mo; Lee, Yong-Keun; Kim, Cheol-We

    2003-01-15

    The aim of this study was to investigate the effect of fluoride gel treatment on the bond strength between titanium alloys and composite resin, and the effect of NaF solution on the bond strength of titanium alloys. Five titanium alloys and one Co-Cr-Mo alloy were tested. Surface of the alloys were treated with three different methods; SiC polishing paper (No. 2000), sandblasting (50-microm Al2O3), and commercially available acidulated phosphate fluoride gel (F-=1.23%, pH 3.0). After treatment, surfaces of alloy were analyzed by SEM/EDXA. A cylindrical gelatin capsule was filled with a light-curable composite resin. The composite resin capsule was placed on the alloy surface after the application of bonding agent, and the composite resin was light cured for 30 s in four different directions. Shear bond strength was measured with the use of an Instron. Fluoride gel did not affect the surface properties of Co-Cr-Mo alloy and Ni-Ti alloy, but other titanium alloys were strongly affected. Alloys treated with the fluoride gel showed similar bond strengths to the alloys treated with sandblasting. Shear bond strength did not show a significant difference (ptitanium alloys. To enhance the bond strength of composite resin to titanium alloys, fluoride-gel treatment may be used as an alternative technique to the sandblasting treatment.

  12. Production of hydroxyapatite layers on the plasma electrolytically oxidized surface of titanium alloys.

    Science.gov (United States)

    Lugovskoy, Alex; Lugovskoy, Svetlana

    2014-10-01

    Hydroxyapatite (HA) is a bioactive material that is widely used for improving the osseointegration of titanium dental implants. Titanium can be coated with HA by various methods, such as chemical vapor deposition (CVD), thermal spray, or plasma spray. HA coatings can also be grown on titanium surfaces by hydrothermal, chemical, and electrochemical methods. Plasma electrolytic oxidation (PEO), or microarc oxidation (MAO), is an electrochemical method that enables the production of a thick porous oxide layer on the surface of a titanium implant. If the electrolyte in which PEO is performed contains calcium and phosphate ions, the oxide layer produced may contain hydroxyapatite. The HA content can then be increased by subsequent hydrothermal treatment. The HA thus produced on titanium surfaces has attractive properties, such as a high porosity, a controllable thickness, and a considerable density, which favor its use in dental and bone surgery. This review summarizes the state of the art and possible further development of PEO for the production of HA on Ti implants.

  13. 21 CFR 73.575 - Titanium dioxide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Titanium dioxide. 73.575 Section 73.575 Food and... ADDITIVES EXEMPT FROM CERTIFICATION Foods § 73.575 Titanium dioxide. (a) Identity. (1) The color additive titanium dioxide is synthetically prepared TiO2, free from admixture with other substances. (2)...

  14. 21 CFR 73.2575 - Titanium dioxide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Titanium dioxide. 73.2575 Section 73.2575 Food and... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2575 Titanium dioxide. (a) Identity and specifications. The color additive titanium dioxide shall conform in identity and specifications to the...

  15. 21 CFR 73.1575 - Titanium dioxide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Titanium dioxide. 73.1575 Section 73.1575 Food and... ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1575 Titanium dioxide. (a) Identity and specifications. (1) The color additive titanium dioxide shall conform in identity and specifications to the...

  16. 40 CFR 180.1195 - Titanium dioxide.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Titanium dioxide. 180.1195 Section 180.1195 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) PESTICIDE PROGRAMS... Titanium dioxide. Titanium dioxide is exempted from the requirement of a tolerance for residues in or...

  17. 21 CFR 73.3126 - Titanium dioxide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Titanium dioxide. 73.3126 Section 73.3126 Food and... ADDITIVES EXEMPT FROM CERTIFICATION Medical Devices § 73.3126 Titanium dioxide. (a) Identity and specifications. The color additive titanium dioxide (CAS Reg. No. 13463-67-7), Color Index No. 77891,...

  18. Practical application of phosphate treatment

    Energy Technology Data Exchange (ETDEWEB)

    Caravaggio, Mike [Integrated Chemistry Solutions Pte. Ltd., Singapore (Singapore)

    2011-05-15

    Phosphate treatment has been applied to subcritical fossil power boilers for well over half a century, as well as being used frequently in heat recovery steam generators. The use of this treatment has evolved over the decades, with the operating sodium to phosphate ratio being the defining factor for the evolution of the treatment. The evolving prescribed sodium to phosphate ratios have been based on the scientific research results and operating experience available at the time, and in the latest EPRI Guidelines issued in 2004 are set at a minimum sodium to phosphate ratio of 3:1, with provision to add up to 1 mg . L{sup -1} of additional free caustic. The ratio limitation has always been set in an effort to minimize the potential for corrosion caused by the potential misapplication of the treatment. Typically, the operating ranges for phosphate treatments are depicted on an x-y plot with the x-axis the phosphate concentration and the y-axis the corrected pH value based on the maximum sodium to phosphate ratio allowed for by the treatment. These operating range plots define the theoretical operating range of a phosphate treatment. This paper briefly discusses the origin of the current phosphate control limits in the EPRI Guidelines, discusses phosphate chemistry, outlines the limitations involved when applying a phosphate treatment and provides additional practical guidance for overcoming these limitations and minimizing the potential for corrosion induced by the incorrect application of a phosphate treatment. (orig.)

  19. Photonuclear reactions on titanium isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Belyshev, S. S. [Moscow State University (Russian Federation); Dzhilavyan, L. Z. [Russian Academy of Sciences, Institute for Nuclear Research (Russian Federation); Ishkhanov, B. S.; Kapitonov, I. M. [Moscow State University (Russian Federation); Kuznetsov, A. A., E-mail: kuznets@depni.sinp.msu.ru; Orlin, V. N.; Stopani, K. A. [Moscow State University, Skobeltsyn Institute of Nuclear Physics (Russian Federation)

    2015-03-15

    The photodisintegration of titanium isotopes in the giant-dipole-resonance energy region is studied by the photon-activation method. Bremsstrahlung photons whose spectrum has the endpoint energy of 55 MeV is used. The yields and integrated cross sections are determined for photoproton reactions on the titanium isotopes {sup 47,48,49,50}Ti. The respective experimental results are compared with their counterparts calculated on the basis of the TALYS code and a combined photonucleon-reaction model. The TALYS code disregards the isospin structure of the giant dipole resonance and is therefore unable to describe the yield of photoproton reactions on the heavy titanium isotopes {sup 49,50}Ti.

  20. Adaptive mesh refinement in titanium

    Energy Technology Data Exchange (ETDEWEB)

    Colella, Phillip; Wen, Tong

    2005-01-21

    In this paper, we evaluate Titanium's usability as a high-level parallel programming language through a case study, where we implement a subset of Chombo's functionality in Titanium. Chombo is a software package applying the Adaptive Mesh Refinement methodology to numerical Partial Differential Equations at the production level. In Chombo, the library approach is used to parallel programming (C++ and Fortran, with MPI), whereas Titanium is a Java dialect designed for high-performance scientific computing. The performance of our implementation is studied and compared with that of Chombo in solving Poisson's equation based on two grid configurations from a real application. Also provided are the counts of lines of code from both sides.

  1. Microanalyses of the hydroxyl-poly-calcium sodium phosphate coatings produced by ion beam assisted deposition

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Thin calcium phosphate coatings on titanium alloy substrates wereprepared by Ar+ ion beam assisted deposition (IBAD) from hydroxyl-poly-calciumsodium phosphate (HPPA) target. The coatings were analyzed by XRD, FTIR, XPS.These analyses revealed that the as-deposited films were amorphous or no apparentcrystallinity. No distinct absorption band of the hydroxyl group was observed in FTIRspectra of the coatings but new absorption bands were presented for CO3-2. Thecalcium to phosphorous ratio of these coatings in different IBAD conditions variedfrom 0.46 to 3.36.

  2. Microanalyses of the hydroxyl—poly—calcium sodium phosphate coatings produced by ion beam assisted deposition

    Institute of Scientific and Technical Information of China (English)

    LIUZhong-Yang; WANGChang-Xing; 等

    2002-01-01

    Thin calcium phosphate catings on titanium alloy substrates were prepared by Ar+ ion beam assisted deposition(IBAD) from hydroxyl-poly-calcium sodium phosphate(HPPA) target.The coatings were analyzed by XRD,FTIR,XPS,These analyses revealed that the as-deposited films were amorphous or no apparent crystallinity.No distinct absorption band of the hydroxyl group was observed in FTIR spectra of the coatings but new absorption bands were presented for CO3-2,The calcium to phosphorous ratio of these catings in different IBAD conditions varied from 0.46 to 3.36.

  3. Degradation processes of reinforced concretes by combined sulfate–phosphate attack

    Energy Technology Data Exchange (ETDEWEB)

    Secco, Michele, E-mail: michele.secco@unipd.it [Inter-Departmental Research Center for the Study of Cement Materials and Hydraulic Binders (CIRCe), University of Padova, Via Gradenigo 6, 35131 Padova (Italy); Department of Civil, Environmental and Architectural Engineering (ICEA), University of Padova, Via Marzolo 9, 35131 Padova (Italy); Lampronti, Giulio Isacco, E-mail: gil21@cam.ac.uk [Department of Earth Sciences, University of Cambridge, Downing Street, CB2 3EQ Cambridge (United Kingdom); Schlegel, Moritz-Caspar, E-mail: moritz-caspar.schlegel@helmholtz-berlin.de [BAM Federal Institute for Materials Research and Testing, Unter den Eichen 87, 12205 Berlin (Germany); Helmholtz-Zentrum Berlin fürMaterialien und Energie GmbH, Hahn-Meitner-Platz 1, 14109 Berlin (Germany); Maritan, Lara, E-mail: lara.maritan@unipd.it [Department of Geosciences, University of Padova, Via Gradenigo 6, 35131 Padova (Italy); Zorzi, Federico, E-mail: federico.zorzi@unipd.it [Department of Geosciences, University of Padova, Via Gradenigo 6, 35131 Padova (Italy)

    2015-02-15

    A novel form of alteration due to the interaction between hydrated cement phases and sulfate and phosphate-based pollutants is described, through the characterization of concrete samples from an industrial reinforced concrete building. Decalcification of the cement matrices was observed, with secondary sulfate and phosphate-based mineral formation, according to a marked mineralogical and textural zoning. Five alteration layers may be detected: the two outermost layers are characterized by the presence of gypsum–brushite solid solution phases associated with anhydrous calcium sulfates and phosphates, respectively, while a progressive increase in apatite and ammonium magnesium phosphates is observable in the three innermost layers, associated with specific apatite precursors (brushite, octacalcium phosphate and amorphous calcium phosphate, respectively). The heterogeneous microstructural development of secondary phases is related to the chemical, pH and thermal gradients in the attacked cementitious systems, caused by different sources of pollutants and the exposure to the sun's radiation.

  4. Phosphates in pallasite meteorites as probes of mantle processes in small planetary bodies

    Science.gov (United States)

    Davis, Andrew M.; Olsen, Edward J.

    1991-01-01

    Trace element analyses of the phosphates minerals in stony-iron pallasite meteorites are used here to investigate the magmatic history of the silicate portions of pallasites. In Eagle Station and seven other pallasites, the phosphates have relatively low concentrations of REEs and are strongly enriched in heavy relative to light REE. These patterns are consistent with formation of phosphate by subsolidus reactions between metal and silicate, in which phosphate inherits the REE pattern of olivine. In Springwater and Santa Rosalia, calcium-rich phosphates have higher concentrations of REE, are enriched in light relative to heavy REE, and have negative europium anomalies. These patterns are consistent with crystallization of phosphate from a europium-depleted chondritic liquid. This is unlikely to have happened near the base of the differentiating parent-body mantle; it suggests that some pallasites may come from regions of their parent bodies much nearer the surface than the core-mantle boundary.

  5. A biomimetic strategy to form calcium phosphate crystals on type I collagen substrate

    Energy Technology Data Exchange (ETDEWEB)

    Xu Zhang [Department of Restorative Dentistry, Faculty of Dentistry, National University of Singapore, 5 Lower Kent Ridge Road 119074, Singapore (Singapore); Neoh, Koon Gee [Department of Chemical and Biomolecular Engineering, National University of Singapore, Kent Ridge 119260, Singapore (Singapore); Kishen, Anil, E-mail: anil.kishen@utoronto.ca [Discipline of Endodontics, Faculty of Dentistry, University of Toronto, 124 Edward Street, Toronto, ON (Canada)

    2010-07-20

    Objective: The aim of this study is to induce mineralization of collagen by introducing phosphate groups onto type I collagen from eggshell membrane (ESM) by treating with sodium trimetaphosphate (STMP). This strategy is based on the hypothesis that phosphate groups introduced on collagen can mimic the nucleating role of phosphorylated non-collagenous proteins bound to collagen for inducing mineralization in natural hard tissue. Method: The collagen membrane was phosphorylated by treating it with a solution of STMP and saturated calcium hydroxide. The phosphorylated collagen was subsequently exposed to a mineralization solution and the pattern of mineralization on the surface of phosphorylated collagen substrate was analyzed. Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), field emission electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD) and microhardness test were used to characterize the collagen substrate and the pattern of minerals formed on the collagen surface. Results: The FTIR and EDX results indicated that the phosphate groups were incorporated onto the collagen surface by treatment with STMP. During the mineralization process, the plate-like mineral, octacalcium phosphate (OCP), which was initially formed on the surface of ESM, was later transformed into needle-like hydroxyapatite (HAP) as indicated by the SEM, FESEM, EDX and XRD findings. The microhardness test displayed significant increase in the Knoop hardness number of the mineralized collagen. Conclusions: Phosphate groups can be introduced onto type I collagen surface by treating it with STMP and such phosphorylated collagen can induce the mineralization of type I collagen.

  6. Calcium Phosphate Biomaterials: An Update

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    Current calcium phosphate (CaP) biomaterials for bone repair, substitution, augmentation and regeneration include hydroxyapatite ( HA ) from synthetic or biologic origin, beta-tricalcium phosphate ( β-TCP ) , biphasic calcium phosphate (BCP), and are available as granules, porous blocks, components of composites (CaP/polymer) cements, and as coatings on orthopedic and dental implants. Experimental calcium phosphate biomaterials include CO3- and F-substituted apatites, Mg-and Zn-substituted β-TCP, calcium phosphate glasses. This paper is a brief review of the different types of CaP biomaterials and their properties such as bioactivity, osteoconductivity, osteoinductivity.

  7. A comparison of the marginal and internal adaptation of titanium and gold-platinum-palladium metal ceramic crowns.

    Science.gov (United States)

    Valderrama, S; Van Roekel, N; Andersson, M; Goodacre, C J; Munoz, C A

    1995-01-01

    The marginal and internal adaptation of metal ceramic crowns fabricated by electrical discharge machining and conventional metal ceramic alloys were compared. The crowns were cemented using zinc phosphate cement, embedded in epoxy resin, and sectioned in two planes: diagonal and buccolingual. The crowns were then measured at nine sites. The results showed that there were no statistical differences between the external marginal opening of the titanium and the gold-platinum-palladium crowns. The overall marginal discrepancies for the restorations in this study were 61 microns (+/- 34 microns) for the titanium metal ceramic crowns and 47 microns (+/- 17 microns) for the gold-platinum-palladium metal ceramic crowns.

  8. Simulation of the effect of citrate exudation from roots on the plant availability of phosphate adsorbed on goethite

    NARCIS (Netherlands)

    Geelhoed, J.S.; Riemsdijk, van W.H.; Findenegg, G.R.

    1999-01-01

    Rhizosphere processes strongly influence the availability of phosphorus (P) to plants. Organic ligands that are exuded from the root surface mobilize phosphorus by dissolution of P minerals or by desorption of adsorbed phosphate. We developed a mechanistic model to study the mobilization of phosphat

  9. Effect of whitening toothpaste on titanium and titanium alloy surfaces.

    Science.gov (United States)

    Faria, Adriana Cláudia Lapria; Bordin, Angelo Rafael de Vito; Pedrazzi, Vinícius; Rodrigues, Renata Cristina Silveira; Ribeiro, Ricardo Faria

    2012-01-01

    Dental implants have increased the use of titanium and titanium alloys in prosthetic applications. Whitening toothpastes with peroxides are available for patients with high aesthetic requirements, but the effect of whitening toothpastes on titanium surfaces is not yet known, although titanium is prone to fluoride ion attack. Thus, the aim of the present study was to compare Ti-5Ta alloy to cp Ti after toothbrushing with whitening and conventional toothpastes. Ti-5Ta (%wt) alloy was melted in an arc melting furnace and compared with cp Ti. Disks and toothbrush heads were embedded in PVC rings to be mounted onto a toothbrushing test apparatus. A total of 260,000 cycles were carried out at 250 cycles/minute under a load of 5 N on samples immersed in toothpaste slurries. Surface roughness and Vickers microhardness were evaluated before and after toothbrushing. One sample of each material/toothpaste was analyzed by Scanning Electron Microscopy (SEM) and compared with a sample that had not been submitted to toothbrushing. Surface roughness increased significantly after toothbrushing, but no differences were noted after toothbrushing with different toothpastes. Toothbrushing did not significantly affect sample microhardness. The results suggest that toothpastes that contain and those that do not contain peroxides in their composition have different effects on cp Ti and Ti-5Ta surfaces. Although no significant difference was noted in the microhardness and roughness of the surfaces brushed with different toothpastes, both toothpastes increased roughness after toothbrushing.

  10. Biomediated continuous release phosphate fertilizer

    Science.gov (United States)

    Goldstein, Alan H.; Rogers, Robert D.

    1999-01-01

    A composition is disclosed for providing phosphate fertilizer to the root zone of plants. The composition comprises a microorganism capable of producing and secreting a solubilization agent, a carbon source for providing raw material for the microorganism to convert into the solubilization agent, and rock phosphate ore for providing a source of insoluble phosphate that is solubilized by the solubilization agent and released as soluble phosphate. The composition is provided in a physical form, such as a granule, that retains the microorganism, carbon source, and rock phosphate ore, but permits water and soluble phosphate to diffuse into the soil. A method of using the composition for providing phosphate fertilizer to plants is also disclosed.

  11. Minerals Yearbook, volume I, Metals and Minerals

    Science.gov (United States)

    ,

    2017-01-01

    The U.S. Geological Survey (USGS) Minerals Yearbook discusses the performance of the worldwide minerals and materials industries and provides background information to assist in interpreting that performance. Content of the individual Minerals Yearbook volumes follows:Volume I, Metals and Minerals, contains chapters about virtually all metallic and industrial mineral commodities important to the U.S. economy. Chapters on survey methods, summary statistics for domestic nonfuel minerals, and trends in mining and quarrying in the metals and industrial mineral industries in the United States are also included.Volume II, Area Reports: Domestic, contains a chapter on the mineral industry of each of the 50 States and Puerto Rico and the Administered Islands. This volume also has chapters on survey methods and summary statistics of domestic nonfuel minerals.Volume III, Area Reports: International, is published as four separate reports. These regional reports contain the latest available minerals data on more than 180 foreign countries and discuss the importance of minerals to the economies of these nations and the United States. Each report begins with an overview of the region’s mineral industries during the year. It continues with individual country chapters that examine the mining, refining, processing, and use of minerals in each country of the region and how each country’s mineral industry relates to U.S. industry. Most chapters include production tables and industry structure tables, information about Government policies and programs that affect the country’s mineral industry, and an outlook section.The USGS continually strives to improve the value of its publications to users. Constructive comments and suggestions by readers of the Minerals Yearbook are welcomed.

  12. Phosphorus availability and microbial immobilization in a Nitisol with the application of mineral and organo-mineral fertilizers

    Directory of Open Access Journals (Sweden)

    FRANCISCO A. MORAIS

    2015-12-01

    Full Text Available ABSTRACT The aim of this study was to evaluate P availability, P and C contained in the microbial biomass, and enzymatic activity (acid phosphatases and β-glucosidases in a Nitisol with the application of mineral and organo-mineral fertilizers. The experiment was performed in a protected environment with control over air temperature and soil moisture. The experimental design was organized in a "5 x 4" factorial arrangement with five sources of P and four times of soil incubation. The sources were: control (without P, triple superphosphate, diammonium phosphate, natural Arad reactive rock phosphate, and organo-mineral fertilizer. The experimental units consisted of PVC columns filled with agricultural soil. The columns were incubated and broken down for analysis at 1, 20, 40, and 60 days after application of the fertilizers. In each column, samples were taken at the layers of 0-2.5, 2.5-5.0, and 5.0-15.0 cm below the zone of the fertilizers. The application of soluble phosphates and organo-mineral fertilizer temporarily increased P availability in the zone near the fertilizers (0-2.5 cm, with maximum availability occurring at approximately 32 days. Microbial immobilization showed behavior similar to P availability, and the greatest immobilizations occurred at approximately 30 days. The organo-mineral fertilizer was not different from soluble phosphates.

  13. Phosphorus availability and microbial immobilization in a Nitisol with the application of mineral and organo-mineral fertilizers.

    Science.gov (United States)

    Morais, Francisco A; Gatiboni, Luciano C

    2015-01-01

    The aim of this study was to evaluate P availability, P and C contained in the microbial biomass, and enzymatic activity (acid phosphatases and β-glucosidases) in a Nitisol with the application of mineral and organo-mineral fertilizers. The experiment was performed in a protected environment with control over air temperature and soil moisture. The experimental design was organized in a "5 x 4" factorial arrangement with five sources of P and four times of soil incubation. The sources were: control (without P), triple superphosphate, diammonium phosphate, natural Arad reactive rock phosphate, and organo-mineral fertilizer. The experimental units consisted of PVC columns filled with agricultural soil. The columns were incubated and broken down for analysis at 1, 20, 40, and 60 days after application of the fertilizers. In each column, samples were taken at the layers of 0-2.5, 2.5-5.0, and 5.0-15.0 cm below the zone of the fertilizers. The application of soluble phosphates and organo-mineral fertilizer temporarily increased P availability in the zone near the fertilizers (0-2.5 cm), with maximum availability occurring at approximately 32 days. Microbial immobilization showed behavior similar to P availability, and the greatest immobilizations occurred at approximately 30 days. The organo-mineral fertilizer was not different from soluble phosphates.

  14. Near-Net Shape Fabrication Using Low-Cost Titanium Alloy Powders

    Energy Technology Data Exchange (ETDEWEB)

    Dr. David M. Bowden; Dr. William H. Peter

    2012-03-31

    The use of titanium in commercial aircraft production has risen steadily over the last half century. The aerospace industry currently accounts for 58% of the domestic titanium market. The Kroll process, which has been used for over 50 years to produce titanium metal from its mineral form, consumes large quantities of energy. And, methods used to convert the titanium sponge output of the Kroll process into useful mill products also require significant energy resources. These traditional approaches result in product forms that are very expensive, have long lead times of up to a year or more, and require costly operations to fabricate finished parts. Given the increasing role of titanium in commercial aircraft, new titanium technologies are needed to create a more sustainable manufacturing strategy that consumes less energy, requires less material, and significantly reduces material and fabrication costs. A number of emerging processes are under development which could lead to a breakthrough in extraction technology. Several of these processes produce titanium alloy powder as a product. The availability of low-cost titanium powders may in turn enable a more efficient approach to the manufacture of titanium components using powder metallurgical processing. The objective of this project was to define energy-efficient strategies for manufacturing large-scale titanium structures using these low-cost powders as the starting material. Strategies include approaches to powder consolidation to achieve fully dense mill products, and joining technologies such as friction and laser welding to combine those mill products into near net shape (NNS) preforms for machining. The near net shape approach reduces material and machining requirements providing for improved affordability of titanium structures. Energy and cost modeling was used to define those approaches that offer the largest energy savings together with the economic benefits needed to drive implementation. Technical

  15. In Situ Laser Coating of Calcium Phosphate on TC4 Surface for Enhancing Bioactivity

    Institute of Scientific and Technical Information of China (English)

    DENG Chi; WANG Yong; ZHANG Ya-ping; GAO Jia-cheng

    2007-01-01

    Titanium alloy has been a successful implant material owing to its excellent ratio of strength to weight,toughness, and bio-inert oxide surface. Significant progress has been made in improving the bioactivity of titanium alloy by coating its oxide surface with calcium phosphates. In the present study, in situ coating was reported on Ti6Al4V(TC4) surface with calcium phosphate (Ca-P) bioceramics synthesized and synchronously cladded by laser beam. This coating was grown by first preplacing directly the raw powders, which contain 80% of CaHPO4 ·2H2O, 20% of CaCO3, and dram of rare earth (RE), on the TC4 surfaces, and then exposing the surfaces to the laser beam with a power density of 12. 73-15.27 MW · m-2 and a scanning velocity of 10. 5 m/s. The resultant coating was characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), thermogravimetric analysis and Different-thermal Scanning (TG-DSC), and Energy Dispersive X-ray Detection (EDX). The results show that these laser ceramics include hydroxyapatite (HA), tricalcium phosphate (TCP), Ca2P2O7, and other Ca-P phases, and the interface between the coating and the TC4 substrate has tighter fixation, in which the chemical bonding is approved. These laser hybrid coatings are useful in enhancing the bioactivity of titanium alloy surfaces.

  16. Osteoblast growth behavior on porous-structure titanium surface

    Energy Technology Data Exchange (ETDEWEB)

    Tian Yuan; Ding Siyang; Peng Hui; Lu Shanming; Wang Guoping [Research Institute of Stomatology, Nanjing Medical University, Nanjing 210029 (China); Xia Lu, E-mail: shelueia@yahoo.com.cn [Research Institute of Stomatology, Nanjing Medical University, Nanjing 210029 (China); Wang Peizhi, E-mail: wangpzi@sina.com [Research Institute of Stomatology, Nanjing Medical University, Nanjing 210029 (China)

    2012-11-15

    Highlights: Black-Right-Pointing-Pointer Micro-arc oxidation technology formed a porous feature on titanium surface. Black-Right-Pointing-Pointer This porous surface accelerated adhesion, proliferation and differentiation compared with smooth surface. Black-Right-Pointing-Pointer Osteogenesis-related proteins and genes were up regulated by this porous surface. Black-Right-Pointing-Pointer It is anticipated that micro-arc oxidation surface could enhance osteoblastic activity and bone regeneration. - Abstract: A bioavailable surface generated by nano-technology could accelerate implant osteointegration, reduce healing time and enable implants to bear early loading. In this study, a nano-porous surface of titanium wafers was modified using micro-arc oxidation technique; surface of smooth titanium was used as control group. Surface characteristic was evaluated by investigating morphology, roughness and hydrophilicity of titanium wafers. In vitro studies, osteoblastic adhesion, proliferation and ALP activity, as well as gene and protein expressions relative to mineralization were assayed. Our results showed that a crater-liked nano-porous surface with greater roughness and better hydrophilicity were fabricated by micro-arc oxidation. It was further indicated that nano-porous surface could enhance adhesion, proliferation and ALP activity of osteoblasts compared with smooth surfaces. In addition, gene and protein expression of collagen-I, osteocalcin and osteopontin were also obviously increased. In summary, micro-arc oxidized techniques could form an irregular nano-porous morphology on implant surface which is favorable to improve osteoblastic function and prospected to be a potent modification of dental implant.

  17. Osteogenic activity of titanium surfaces with nanonetwork structures

    Directory of Open Access Journals (Sweden)

    Xing H

    2014-04-01

    Full Text Available Helin Xing,1,2 Satoshi Komasa,3 Yoichiro Taguchi,4 Tohru Sekino,5 Joji Okazaki3 1Department of Prosthetic Dentistry, School of Stomatology, The Fourth Military Medical University, Xi’an, People’s Republic of China; 2Graduate School of Dentistry (Removable Prosthodontics and Occlusion, 3Department of Removable Prosthodontics and Occlusion, 4Department of Periodontology, Osaka Dental University, Hirakata, Osaka, Japan; 5Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Aoba-ku, Sendai, Japan Background: Titanium surfaces play an important role in affecting osseointegration of dental implants. Previous studies have shown that the titania nanotube promotes osseointegration by enhancing osteogenic differentiation. Only relatively recently have the effects of titanium surfaces with other nanostructures on osteogenic differentiation been investigated. Methods: In this study, we used NaOH solutions with concentrations of 2.5, 5.0, 7.5, 10.0, and 12.5 M to develop a simple and useful titanium surface modification that introduces the nanonetwork structures with titania nanosheet (TNS nanofeatures to the surface of titanium disks. The effects of such a modified nanonetwork structure, with different alkaline concentrations on the osteogenic differentiation of rat bone marrow mesenchymal stem cells (BMMSCs, were evaluated. Results: The nanonetwork structures with TNS nanofeatures induced by alkali etching markedly enhanced BMMSC functions of cell adhesion and osteogenesis-related gene expression, and other cell behaviors such as proliferation, alkaline phosphatase activity, extracellular matrix deposition, and mineralization were also significantly increased. These effects were most pronounced when the concentration of NaOH was 10.0 M. Conclusion: The results suggest that nanonetwork structures with TNS nanofeatures improved BMMSC proliferation and induced BMMSC osteogenic differentiation. In addition, the surfaces formed

  18. Nanodispersed boriding of titanium alloy

    Directory of Open Access Journals (Sweden)

    Kateryna O. Kostyk

    2015-12-01

    Full Text Available The problem of improving the operational reliability of machines is becoming increasingly important due to the increased mechanical, thermal and other loads on the details. There are many surface hardening methods for machines parts which breakdown begins with surface corruption. The most promising methods are chemo-thermal treatment. Aim: The aim of this work is to study the impact of boriding on the structure and properties of titanium alloy. Materials and Methods: The material of this study is VT3-1 titanium alloy. The boriding were conducted using nanodispersed powder blend based on boric substances. Results: It is established that boriding of paste compounds allows obtaining the surface hardness within 30...29 GPa and with declining to 27...26 GPa in layer to the transition zone (with total thickness up to 110 μm owing to changes of the layer phase composition where Ti2B, TiB, TiB2 titanium borides are formed. The increasing of chemical-thermal treatment time from 15 minutes to 2 hours leads to thickening of the borated layer (30...110 µm and transition zone (30...190 µm. Conclusions: Due to usage of nanodispersed boric powder, the boriding duration is decreasing in 2...3 times. This allows saving time and electric energy. The developed optimal mode of boriding the VT3-1 titanium alloy allows obtaining the required operational characteristics and to combine the saturation of the surface layer with atomic boron and hardening.

  19. Wind-wave affected phosphate loading variations and their relationship to redox condition in Lake Taihu

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Variation of wind speed and the physico-chemical parameters, such as dissolved phosphate, ferrous and manganese in lake water were observed on site. Together with the chemistry analysis and simulated experiment in lab, the change of phosphate concentration in lake water was analyzed. The variation of ferrous/phosphate ratio explained that along with the enhancement of wind-wave effect and the oxidation ability of lake water, the effects of co-precipitation and removal of dissolved phosphate and iron in the lake water were reinforced. The ferrous/phosphate ratio in pore water was less than 2.0, demonstrating that the dissolved phosphate can be released into the overlying water. But, in the lake water, the stability of phosphate was controlled by the water dynamics.The phosphate release experiment showed that molecular release was only part of the whole and the direct discharge of phosphate in the pore water was also a part. The mineralization and biological process of suspended particulates in the water may be another important reason for the whole phosphate loadings.

  20. Miscellaneous Industrial Mineral Operations

    Data.gov (United States)

    Department of Homeland Security — This map layer includes miscellaneous industrial minerals operations in the United States. The data represent commodities covered by the Minerals Information Team...

  1. Total Phosphate Influences the Rate of Hydrocarbon Degradation but Phosphate Mineralogy Shapes Microbial Community Composition in Cold-Region Calcareous Soils.

    Science.gov (United States)

    Siciliano, Steven D; Chen, Tingting; Phillips, Courtney; Hamilton, Jordan; Hilger, David; Chartrand, Blaine; Grosskleg, Jay; Bradshaw, Kris; Carlson, Trevor; Peak, Derek

    2016-05-17

    Managing phosphorus bioaccessibility is critical for the bioremediation of hydrocarbons in calcareous soils. This paper explores how soil mineralogy interacts with a novel biostimulatory solution to both control phosphorus bioavailability and influence bioremediation. Two large bore infiltrators (1 m diameter) were installed at a PHC contaminated site and continuously supplied with a solution containing nutrients and an electron acceptor. Soils from eight contaminated sites were prepared and pretreated, analyzed pretrial, spiked with diesel, placed into nylon bags into the infiltrators, and removed after 3 months. From XAS, we learned that three principal phosphate phases had formed: adsorbed phosphate, brushite, and newberyite. All measures of biodegradation in the samples (in situ degradation estimates, mineralization assays, culturable bacteria, catabolic genes) varied depending upon the soil's phosphate speciation. Notably, adsorbed phosphate increased anaerobic phenanthrene degradation and bzdN catabolic gene prevalence. The dominant mineralogical constraints on community composition were the relative amounts of adsorbed phosphate, brushite, and newberyite. Overall, this study finds that total phosphate influences microbial community phenotypes whereas relative percentages of phosphate minerals influences microbial community genotype composition.

  2. Soil phosphate stable oxygen isotopes across rainfall and bedrock gradients.

    Science.gov (United States)

    Angert, Alon; Weiner, Tal; Mazeh, Shunit; Sternberg, Marcelo

    2012-02-21

    The stable oxygen isotope compositions of soil phosphate (δ(18)O(p)) were suggested recently to be a tracer of phosphorus cycling in soils and plants. Here we present a survey of bioavailable (resin-extractable or resin-P) inorganic phosphate δ(18)O(p) across natural and experimental rainfall gradients, and across soil formed on sedimentary and igneous bedrock. In addition, we analyzed the soil HCl-extractable inorganic δ(18)O(p), which mainly represents calcium-bound inorganic phosphate. The resin-P values were in the range 14.5-21.2‰. A similar range, 15.6-21.3‰, was found for the HCl-extractable inorganic δ(18)O(p), with the exception of samples from a soil of igneous origin that show lower values, 8.2-10.9‰, which indicate that a large fraction of the inorganic phosphate in this soil is still in the form of a primary mineral. The available-P δ(18)O(p) values are considerably higher than the values we calculated for extracellular hydrolysis of organic phosphate, based on the known fractionation from lab experiments. However, these values are close to the values expected for enzymatic-mediated phosphate equilibration with soil-water. The possible processes that can explain this observation are (1) extracellular equilibration of the inorganic phosphate in the soil; (2) fractionations in the soil are different than the ones measured at the lab; (3) effect of fractionation during uptake; and (4) a flux of intercellular-equilibrated inorganic phosphate from the soil microbiota, which is considerably larger than the flux of hydrolyzed organic-P.

  3. Minerals processing opportunities for New South Wales and Australia

    Energy Technology Data Exchange (ETDEWEB)

    Fraser, R. (Pasminco Mining, NSW (Australia))

    1991-03-01

    An account is given of the main findings and recommendations of a report presented in September 1990 by the NSW Task Force on Mineral Processing Development Strategies. The Task Force considered that the best opportunities fell into two categories: existing industries with development potential (steel, aluminium, refractories, zinc, lead, copper, coke, dimension stone and gemstones) and new opportunities (in processing of titanium, titanium dioxide pigment, rare earths, silicon, fused silica, advanced ceramics, mullite and magnesium). Potential for development of the minerals is discussed. Australia is seen as being in an excellent position to capitalize on recent economic changes and new technolgies. Coal, except for value-added coal products and petroleum were excluded from the study - a separate task force has been set up to consider the NSW coal industry. 1 ref., 2 figs., 1 tab.

  4. Uranium Extraction from Syrian Phosphate: A case Study

    Directory of Open Access Journals (Sweden)

    J.STAS, I. OTHMAN

    2010-12-01

    Full Text Available Uranium and trace elements were studied in few hundred samples from phosphatic formations in Syria. Uranium and trace elements were enriched in phosphorites facies compared to carbonate and siliceous facies. Uranium content of Syrian phosphorite by fission track method shows that uranium is related to the apatite mineral and organic matter. The concentration of uranium in phosphatic elements depends on the quality of these elements (grains, biogenic-elements. Further, uranium is relatively mobile during biomicritisation, coating and weathering. Investigation of uranium extraction from phosphoric acid produced at Homs plant (G.F.S by using phosphate concentrate from Khneifiss and Charquieh mines, have been carried out in a micro pilot and pilot plant scales. The result shows that the yield of uranium extraction from H3 PO4 is more than 95%.

  5. New titanium and titanium/hydroxyapatite coatings on ultra-high-molecular-weight polyethylene-in vitro osteoblastic performance

    Energy Technology Data Exchange (ETDEWEB)

    Silva, M A; Lopes, M A; Santos, J D; Fernandes, M H [Department of Metallurgical and Materials Engineering, Materials Section-Faculty of Engineering, University of Porto (Portugal); Gomes, P S [Laboratory of Pharmacology and Cellular Biocompatibility-Faculty of Dental Medicine, University of Porto (Portugal); Vila, M; Silva, R F, E-mail: mhfernandes@fmd.up.p [Department of Ceramics and Glass Engineering, University of Aveiro, CICECO (Portugal)

    2010-06-15

    The development of optimized hip joint materials is one of the most challenging opportunities in prosthetic technologies. In current approaches, ultra-high-molecular-weight polyethylene (UHMWPE) has been a favorite material for the acetabular component and, regarding the cementless technique, several coating options may be considered to contain and stabilize bearing surfaces and establish an improved interface with bone. In this work, newly developed constructs of UHMWPE coated with either commercially pure titanium (cpTi-UHMWPE), by DC magnetron sputtering, or with commercially pure titanium and hydroxyapatite (cpTi/HA-UHMWPE), by DC/RF magnetron co-sputtering, have been prepared and biologically characterized with human bone marrow-derived osteoblastic cultures. The cpTi-UHMWPE samples allowed a high cell growth and the expression of the complete osteoblastic phenotype, with high alkaline phosphatase activity, expression of osteogenic-associated genes and evident cell-mediated mineralization of the extracellular matrix. In comparison, the cpTi/HA-UHMWPE samples reported lower cell proliferation but earlier cell-mediated matrix mineralization. Accordingly, these newly developed systems may be suitable candidates to improve the osteointegration process in arthroplastic devices; nevertheless, further biological evaluation should be conducted.

  6. Biomimetic calcium phosphate coatings on recombinant spider silk fibres

    Energy Technology Data Exchange (ETDEWEB)

    Yang Liang; Habibovic, Pamela; Van Blitterswijk, Clemens A [Department of Tissue Regeneration, University of Twente, PO Box 217, 7500 AE Enschede (Netherlands); Hedhammar, My; Johansson, Jan [Department of Anatomy, Physiology and Biochemistry, Swedish University of Agricultural Sciences, the Biomedical Centre, Box 575, 751 23 Uppsala (Sweden); Blom, Tobias; Leifer, Klaus [Department of Engineering Sciences, Uppsala University, Box 534, S-751 21 Uppsala (Sweden)

    2010-08-01

    Calcium phosphate ceramic coatings, applied on surfaces of metallic and polymeric biomaterials, can improve their performance in bone repair and regeneration. Spider silk is biocompatible, strong and elastic, and hence an attractive biomaterial for applications in connective tissue repair. Recently, artificial spider silk, with mechanical and structural characteristics similar to those of native spider silk, has been produced from recombinant minispidroins. In the present study, supersaturated simulated body fluid was used to deposit calcium phosphate coatings on recombinant spider silk fibres. The mineralization process was followed in time using scanning electron microscopy equipped with an energy dispersive x-ray (EDX) detector and Raman spectroscope. Focused ion beam technology was used to produce a cross section of a coated fibre, which was further analysed by EDX. Preliminary in vitro experiments using a culture of bone marrow-derived human mesenchymal stem cells (hMSCs) on coated fibres were also performed. This study showed that recombinant spider silk fibres were successfully coated with a homogeneous and thick crystalline calcium phosphate layer. In the course of the mineralization process from modified simulated body fluid, sodium chloride crystals were first deposited on the silk surface, followed by the deposition of a calcium phosphate layer. The coated silk fibres supported the attachment and growth of hMSCs.

  7. Respiratory health risks among nonmetal miners.

    Science.gov (United States)

    Short, S R; Petsonk, E L

    1993-01-01

    The risks of occupational respiratory disease faced by nonmetal miners are the focus of this review. An understanding of the respiratory risks requires an understanding of the minerology of the ground and rock around the materials being mined. Relevant exposures encompass radon gas and deisel fumes, as well as mineral and rock dusts, including free silica. The types of materials mined and their associated health effects are examined, including the silicates (fibrous silicates such as asbestos, asbestiform fibrous minerals such as wollastonite and fuller's earth, and nonfibrous silicates such as talc and kaolin), sedimentary precipitates such as phosphates, potash, gypsum, and salt, as well as hydrocarbon-containing sedimentary rock such as oil shale.

  8. Pyridoxal phosphate-dependent neonatal epileptic encephalopathy.

    Science.gov (United States)

    Bagci, S; Zschocke, J; Hoffmann, G F; Bast, T; Klepper, J; Müller, A; Heep, A; Bartmann, P; Franz, A R

    2008-03-01

    Pyridox(am)ine-5'-phosphate oxidase converts pyridoxine phosphate and pyridoxamine phosphate to pyridoxal phosphate, a cofactor in many metabolic reactions, including neurotransmitter synthesis. A family with a mutation in the pyridox(am)ine-5'-phosphate oxidase gene presenting with neonatal seizures unresponsive to pyridoxine and anticonvulsant treatment but responsive to pyridoxal phosphate is described. Pyridoxal phosphate should be considered in neonatal epileptic encephalopathy unresponsive to pyridoxine.

  9. Pyridoxal phosphate-dependent neonatal epileptic encephalopathy

    OpenAIRE

    2009-01-01

    Pyridox(am)ine-5′-phosphate oxidase converts pyridoxine phosphate and pyridoxamine phosphate to pyridoxal phosphate, a cofactor in many metabolic reactions, including neurotransmitter synthesis. A family with a mutation in the pyridox(am)ine-5′-phosphate oxidase gene presenting with neonatal seizures unresponsive to pyridoxine and anticonvulsant treatment but responsive to pyridoxal phosphate is described. Pyridoxal phosphate should be considered in neonatal epileptic encephalopathy unrespons...

  10. Solid state NMR study of bone mineral

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Y.

    1992-01-01

    In high field (9.4 T) CP MASS (cross polarization magic angle sample spinning) studies, in contrast to the scheme in the literature that infers the presence of minor constituents in spectra, we developed a new scheme to suppress the main part of the spectra to show the minor constituents. In order to perform in vivo solid state NMR studies, a double tuned two port surface coil probe was constructed. This probe is a modified version of the traditional Cross probe, which utilizes two 1/4 wave length 50 ohm transmission line, one with open ended and the other with shorted end, to isolate the high and low frequency circuits. The two resonance frequencies in Cross probe were proton and carbon. Our probe is designed to resonate at the proton and phosphorus frequencies, which are much closer to each other and hence more difficult to be tuned and matched simultaneously. Our approach to solve this problem is that instead of using standard 50 ohm transmission lines, we constructed a low capacity open end coaxial transmission line and low inductance shorted end coaxial transmission line. The Q of the phosphorus channel is high. We developed a short contact time cross polarization technique for non-MASS spectroscopy which reduces the signal of the major component of bone mineral to emphasize the minor component. By applying this technique on intact pork bone samples with our home made surface coil, we observed the wide line component, acid phosphate, for the first time. Hydroxyapatite, brushite and octacalcium are considered in the literature to be the model compounds for bone mineral. Cross polarization dynamics has been studied on hydroxyapatite and brushite, which yielded an NMR value for the distance between proton and phosphorus. One and two dimensional CP MASS spectroscopy of octacalcium phosphate were also studied, which revealed the different cross polarization rates and anisotropic channel shifts of acid phosphate and phosphate ions in octacalcium phosphate.

  11. Mineralization by inhibitor exclusion: the calcification of collagen with fetuin.

    Science.gov (United States)

    Price, Paul A; Toroian, Damon; Lim, Joo Eun

    2009-06-19

    One of our goals is to understand the mechanisms that deposit mineral within collagen fibrils, and as a first step we recently determined the size exclusion characteristics of the fibril. This study revealed that apatite crystals up to 12 unit cells in size can access the water within the fibril, whereas molecules larger than a 40-kDa protein are excluded. Based on these observations, we proposed a novel mechanism for fibril mineralization: that macromolecular inhibitors of apatite growth favor fibril mineralization by selectively inhibiting crystal growth in the solution outside of the fibril. To test this mechanism, we developed a system in which crystal formation is driven by homogeneous nucleation at high calcium phosphate concentration and the only macromolecule in solution is fetuin, a 48-kDa inhibitor of apatite growth. Our experiments with this system demonstrated that fetuin determines the location of mineral growth; in the presence of fetuin mineral grows exclusively within the fibril, whereas in its absence mineral grows in solution outside the fibril. Additional experiments showed that fetuin is also able to localize calcification to the interior of synthetic matrices that have size exclusion characteristics similar to those of collagen and that it does so by selectively inhibiting mineral growth outside of these matrices. We termed this new calcification mechanism "mineralization by inhibitor exclusion," the selective mineralization of a matrix using a macromolecular inhibitor of mineral growth that is excluded from that matrix. Future studies will be needed to evaluate the possible role of this mechanism in bone mineralization.

  12. High-pressure minerals in shocked meteorites

    Science.gov (United States)

    Tomioka, Naotaka; Miyahara, Masaaki

    2017-09-01

    Heavily shocked meteorites contain various types of high-pressure polymorphs of major minerals (olivine, pyroxene, feldspar, and quartz) and accessory minerals (chromite and Ca phosphate). These high-pressure minerals are micron to submicron sized and occur within and in the vicinity of shock-induced melt veins and melt pockets in chondrites and lunar, howardite-eucrite-diogenite (HED), and Martian meteorites. Their occurrence suggests two types of formation mechanisms (1) solid-state high-pressure transformation of the host-rock minerals into monomineralic polycrystalline aggregates, and (2) crystallization of chondritic or monomineralic melts under high pressure. Based on experimentally determined phase relations, their formation pressures are limited to the pressure range up to 25 GPa. Textural, crystallographic, and chemical characteristics of high-pressure minerals provide clues about the impact events of meteorite parent bodies, including their size and mutual collision velocities and about the mineralogy of deep planetary interiors. The aim of this article is to review and summarize the findings on natural high-pressure minerals in shocked meteorites that have been reported over the past 50 years.

  13. Biomimetic Mineralization of Recombinamer-Based Hydrogels toward Controlled Morphologies and High Mineral Density.

    Science.gov (United States)

    Li, Yuping; Chen, Xi; Fok, Alex; Rodriguez-Cabello, Jose Carlos; Aparicio, Conrado

    2015-11-25

    The use of insoluble organic matrices as a structural template for the bottom-up fabrication of organic-inorganic nanocomposites is a powerful way to build a variety of advanced materials with defined and controlled morphologies and superior mechanical properties. Calcium phosphate mineralization in polymeric hydrogels is receiving significant attention in terms of obtaining biomimetic hierarchical structures with unique mechanical properties and understanding the mechanisms of the biomineralization process. However, integration of organic matrices with hydroxyapatite nanocrystals, different in morphology and composition, has not been well-achieved yet at nanoscale. In this study, we synthesized thermoresponsive hydrogels, composed of elastin-like recombinamers (ELRs), to template mineralization of hydroxyapatite nanocrystals using a biomimetic polymer-induced liquid-precursor (PILP) mineralization process. Different from conventional mineralization where minerals were deposited on the surface of organic matrices, they were infiltrated into the frameworks of ELR matrices, preserving their microporous structure. After 14 days of mineralization, an average of 78 μm mineralization depth was achieved. Mineral density up to 1.9 g/cm(3) was found after 28 days of mineralization, which is comparable to natural bone and dentin. In the dry state, the elastic modulus and hardness of the mineralized hydrogels were 20.3 ± 1.7 and 0.93 ± 0.07 GPa, respectively. After hydration, they were reduced to 4.50 ± 0.55 and 0.10 ± 0.03 GPa, respectively. These values were lower but still on the same order of magnitude as those of natural hard tissues. The results indicated that inorganic-organic hybrid biomaterials with controlled morphologies can be achieved using organic templates of ELRs. Notably, the chemical and physical properties of ELRs can be tuned, which might help elucidate the mechanisms by which living organisms regulate the mineralization process.

  14. Determinants of pathologic mineralization.

    Science.gov (United States)

    Kirsch, Thorsten

    2008-01-01

    Physiologic mineralization is necessary for the formation of skeletal tissues and for their appropriate functions during adulthood. Mineralization has to be controlled and restricted to specific regions. If the mineralization process occurs in regions that normally do not mineralize, there can be severe consequences (pathologic or ectopic mineralization). Recent findings have indicated that physiologic and pathologic mineralization events are initiated by matrix vesicles, membrane-enclosed particles released from the plasma membranes of mineralization-competent cells. The understanding of how these vesicles are released from the plasma membrane and initiate the mineralization process may provide novel therapeutic strategies to prevent pathologic mineralization. In addition, other regulators (activators and inhibitors) of physiologic mineralization have been identified and characterized, and there is evidence that the same factors also contribute to the regulation of pathologic mineralization. Finally, programmed cell death (apoptosis) may be a contributor to physiologic mineralization and if occurring after tissue injury may induce pathologic mineralization and mineralization-related differentiation events in the injured and surrounding areas. This review describes how the understanding of mechanisms and factors regulating physiologic mineralization can be used to develop new therapeutic strategies to prevent pathologic or ectopic mineralization events.

  15. Osteogenic activity and antibacterial effect of porous titanium modified with metal-organic framework films.

    Science.gov (United States)

    Chen, Junyu; Zhang, Xin; Huang, Chao; Cai, He; Hu, Shanshan; Wan, Qianbing; Pei, Xibo; Wang, Jian

    2017-03-01

    As a new class of crystalline nanoporous materials, metal-organic frameworks (MOFs) have recently been used for biomedical applications due to their large surface area, high porosity, and theoretically infinite structures. To improve the biological performance of titanium, MOF films were applied to surface modification of titanium. Zn-based MOF films composed of zeolitic imidazolate framework-8 (ZIF-8) crystals with nanoscale and microscale sizes (nanoZIF-8 and microZIF-8) were prepared on porous titanium surfaces by hydrothermal and solvothermal methods, respectively. The ZIF-8 films were characterized by powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The nanoZIF-8 film exhibited good biocompatibility, whereas the microZIF-8 film showed obvious cytotoxicity to MG63 cells. Compared to pure titanium and alkali- and heat-treated porous titanium, the nanoZIF-8 film not only enhanced alkaline phosphatase (ALP) activity, extracellular matrix mineralization, and expression of osteogenic genes (ALP, Runx2) in MG63 cells but also inhibited the growth of Streptococcus mutans. These results indicate that MOF films or coatings may be promising candidates for bone tissue engineering. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 834-846, 2017.

  16. Synthesis and Characterization of Titanium Slag from Ilmenite by Thermal Plasma Processing

    Science.gov (United States)

    Samal, Sneha

    2016-09-01

    Titanium rich slag has emerged as a raw material for alternative titanium source. Ilmenite contains 42-50% TiO2 as the mineralogical composition depending on the geographical resources. Application of titanium in paper, plastic, pigment and other various industries is increasing day by day. Due to the scarcity of natural raw mineral rutile (TiO2), ilmenite is considered as precursor for the extraction of TiO2. Ilmenite is reduced at the initial stage for the conversion of complex iron oxide into simpler form. Therefore, pre-reduction of ilmenite concentrate is essential to minimize the energy consumption during thermal plasma process. Thermal plasma processing of ilmenite for the production of titania rich slag is considered to be the direct route to meet the current demand of industrial needs of titanium. Titania rich slag contains 70-80% TiO2 as the major component with some other minor impurities, like oxide phases of Si, Al, Cr, Mg, Mn, Ca, etc. Usually titanium is present in tetravalent forms with globular metallic iron in the slag. Titania rich slag undergoes leaching for the removal of iron and transforming the slag into synthetic rutile having 85-95% of TiO2.

  17. Nanocoating of titanium implant surfaces with organic molecules. Polysaccharides including glycosaminoglycans

    DEFF Research Database (Denmark)

    Gurzawska, Katarzyna Aleksandra; Svava, Rikke; Jørgensen, Niklas Rye;

    2012-01-01

    Long-term stability of titanium implants are dependent on a variety of factors. Nanocoating with organic molecules is one of the method used to improve osseointegration. Nanoscale modification of titanium implants affects surface properties, such as hydrophilicity, biochemical bonding capacity...... and roughness. This influences cell behaviour on the surface such as adhesion, proliferation and differentiation of cells as well as the mineralization of the extracellular matrix at the implant surfaces. The aim of the present systematic review was to describe organic molecules used for surface nanocoating...... nanocoatings. The included in vivo studies, showed improvement of bone interface reactions measured as increased Bone-to-Implant Contact length and Bone Mineral Density adjacent to the polysaccharide coated surfaces. Based on existing literature, surface modification with polysaccharide and glycosaminoglycans...

  18. Preparation of magnesium phosphate cement by recycling the product of thermal transformation of asbestos containing wastes

    OpenAIRE

    2014-01-01

    Asbestos containing wastes have been employed for the first time in the formulation of magnesium phosphate cements. Two samples were mixed with magnesium carbonate and calcined at 1100 and 1300 C. Under these conditions, complete destruction of asbestos minerals is known to occur. The product, containing MgO, after reaction with water-soluble potassium di-hydrogen phosphate, led to the formation of hydrated phases at room temperature. Crystalline and amorphous reaction products were detected,...

  19. Citrate adsorption can decrease soluble phosphate concentration in soil : experimental and modeling evidence

    OpenAIRE

    Duputel, M.; Van Hoye, F.; Toucet, Joële; F. Gerard

    2013-01-01

    The adsorption/desorption of phosphate (PO4) on soil minerals is a major process regulating soluble phosphate concentrations (i.e. phosphorus availability) and ultimately PO4 bio-availability. Release of citrate by roots is widely recognized as an effective biological mechanism for increasing available phosphorus (P) in soil. However, interactions between citrate and PO4 are poorly understood and little investigated in soils. Using surface complexation modeling we recently predicted that citr...

  20. Antimicrobial titanium/silver PVD coatings on titanium

    Directory of Open Access Journals (Sweden)

    Thull Roger

    2006-03-01

    Full Text Available Abstract Background Biofilm formation and deep infection of endoprostheses is a recurrent complication in implant surgery. Post-operative infections may be overcome by adjusting antimicrobial properties of the implant surface prior to implantation. In this work we described the development of an antimicrobial titanium/silver hard coating via the physical vapor deposition (PVD process. Methods Coatings with a thickness of approximately 2 μm were deposited on titanium surfaces by simultaneous vaporisation of both metals in an inert argon atmosphere with a silver content of approximately 0.7 – 9% as indicated by energy dispersive X-ray analysis. On these surfaces microorganisms and eukaryotic culture cells were grown. Results The coatings released sufficient silver ions (0.5–2.3 ppb when immersed in PBS and showed significant antimicrobial potency against Staphylococcus epidermis and Klebsiella pneumoniae strains. At the same time, no cytotoxic effects of the coatings on osteoblast and epithelial cells were found. Conclusion Due to similar mechanical performance when compared to pure titanium, the TiAg coatings should be suitable to provide antimicrobial activity on load-bearing implant surfaces.

  1. Fabrication and biocompatibility in vitro of potassium titanate biological thin film/titanium alloy biological composite

    Institute of Scientific and Technical Information of China (English)

    QI Yumin; HE Yun; CUI Chunxiang; LIU Shuangjin; WANG Huifen

    2007-01-01

    A potassium titanate biological thin film/titanium alloy biological composite was fabricated by way of bionic chemistry.The biocompatibility fn vitro of Ti-15Mo-3Nb and the potassium titanate biological thin film/titanium alloy was studied using simulated body fluid cultivation,kinetic clotting of blood and osteoblast cell cultivation experiments in vitro.By comparing the biological properties of both materials,the following conclusions can be obtained:(1)The deposition of a calcium phosphate layer was not found on the surface of Ti-15Mo-3Nb,so it was bioinert.Because the network of potassium titanate biological thin film could induce the deposition of a calcium phosphate layer,this showed that it had excellent bioactivity.(2)According to the values of kinetic clotting,the blood coagulation time of the potassium titanate biological thin film was more than that of Ti-15Mo-3Nb.It was obvious that the potassium titanate biological thin film possessed good hemocompatibility.(3)The cell compatibility of both materials was very good.However,the growth trend and multiplication of osteoblast cells on the surface of potassium titanate biological thin film was better,which made for the concrescence of wounds during the earlier period.As a result,the potassium titanate biological thin film/titanium alloy showed better biocompatibility and bioactivity.

  2. Manufacture of nanosized apatite coatings on titanium with different surface treatments using a supersaturated calcification solution

    Directory of Open Access Journals (Sweden)

    Adrian Paz Ramos

    Full Text Available The biomimetic method is used for the deposition of calcium phosphate coatings (Ca - P on the surface of different biomaterials. However, the application of this method requires long exposure times in order to obtain a suitable layer thickness for its use in medical devices. In this paper, we present a fast approach to obtain apatite coatings on titanium, using a combination of supersaturated calcification solution (SCS with chemical modification of the titanium surface. Also, it was evaluated the effect of four different surface treatments on the apatite deposition rate. Commercially pure titanium plates were activated by chemical or thermochemical treatments. Then, the activated samples were immersed in a solution with high content of calcium and phosphate ions at 37 ºC for 24 h, mimicking the physiological conditions. The coatings were studied by Fourier transform infrared spectroscopy (FTIR, X-ray diffraction (XRD, scanning electron microscopy (SEM and energy dispersive X-ray spectroscopy (EDX. The use of SCS solutions allowed the formation of crystalline hydroxyapatite coatings within a period of 24 h with a thickness between 1 and 5.3 µm. Besides, precipitates of hydroxyapatite nanoparticles with a globular configuration, forming aggregates with submicrometer size, were found in SCS solutions.

  3. 30 CFR 46.6 - Newly hired experienced miner training.

    Science.gov (United States)

    2010-07-01

    ... TRAINING TRAINING AND RETRAINING OF MINERS ENGAGED IN SHELL DREDGING OR EMPLOYED AT SAND, GRAVEL, SURFACE STONE, SURFACE CLAY, COLLOIDAL PHOSPHATE, OR SURFACE LIMESTONE MINES. § 46.6 Newly hired experienced...) Instruction on the recognition and avoidance of electrical hazards and other hazards present at the mine,...

  4. Mineral deposits in western Saudi Arabia; a preliminary report

    Science.gov (United States)

    Roberts, Ralph Jackson; Greenwood, William R.; Worl, Ronald G.; Dodge, F.C.W.; Kiilsgaard, Thor H.

    1975-01-01

    Mineral deposits in Saudi Arabia include a variety of deposits which were formed in many geologic environments. These include magmatic and late magmatic deposits in igneous masses, contact metamorphic deposits along the margins of igneous bodies, and stratiform sulfide deposits and veins. Notable deposits of sedimentary origin include deposits of iron oxides and phosphate.

  5. Electrochemical deposition of mineralized BSA/collagen coating.

    Science.gov (United States)

    Zhuang, Junjun; Lin, Jun; Li, Juan; Wang, Huiming; Cheng, Kui; Weng, Wenjian

    2016-09-01

    In this work, mineralized collagen coatings with different loading quantity of bovine serum albumin (BSA) were prepared via in situ electrochemical deposition on titanium substrate. The microstructure and BSA loading quantity of the coatings could be controlled by the electrochemical deposition parameters, such as deposition potential, BSA concentration and its adding sequence in the electrolyte. The BSA loading quantity in the coatings was obtained in the range of 0.0170-0.173mg/cm(2), enhancing the cell adhesion and proliferation of the coatings with the simultaneous release. The distinct release behaviors of BSA were attributed to their gradient distribution with different mineralization degrees, which could be adjusted by the deposition process. These results suggest that in situ electrochemical deposition is a promising way to incorporate functional molecules into the mineralized collagen coatings and the mineralized BSA/collagen coatings are highly promising for improving the rhBMP-2 loading capability (1.8-fold).

  6. Hydrogen content in titanium and a titanium-zirconium alloy after acid etching.

    Science.gov (United States)

    Frank, Matthias J; Walter, Martin S; Lyngstadaas, S Petter; Wintermantel, Erich; Haugen, Håvard J

    2013-04-01

    Dental implant alloys made from titanium and zirconium are known for their high mechanical strength, fracture toughness and corrosion resistance in comparison with commercially pure titanium. The aim of the study was to investigate possible differences in the surface chemistry and/or surface topography of titanium and titanium-zirconium surfaces after sand blasting and acid etching. The two surfaces were compared by X-ray photoelectron spectroscopy, secondary ion mass spectroscopy, scanning electron microscopy and profilometry. The 1.9 times greater surface hydrogen concentration of titanium zirconium compared to titanium was found to be the major difference between the two materials. Zirconium appeared to enhance hydride formation on titanium alloys when etched in acid. Surface topography revealed significant differences on the micro and nanoscale. Surface roughness was increased significantly (pzirconium alloy. High-resolution images showed nanostructures only present on titanium zirconium.

  7. Coastal deposits of heavy mineral sands; Global significance and US resources

    Science.gov (United States)

    Van Gosen, Bradley S.; Bleiwas, Donald I.; Bedinger, George M.; Ellefsen, Karl J.; Shah, Anjana K.

    2016-01-01

    Ancient and modern coastal deposits of heavy mineral sands (HMS) are the principal source of several heavy industrial minerals, with mining and processing operations on every continent except Antarctica. For example, HMS deposits are the main source of titanium feedstock for the titanium dioxide (TiO2) pigments industry, obtained from the minerals ilmenite (Fe2+TiO3), rutile (TiO2) and leucoxene (an alteration product of ilmenite). HMS deposits are also the principal source of zircon (ZrSiO4), from which zirconium dioxide (ZrO2) is obtained for uses mostly in refractory products. Sometimes monazite [(Ce,La,Nd,Th)PO4] is recovered as a byproduct mineral, sought for its rare earth elements and thorium (Ault and others, 2016; Sengupta and Van Gosen, 2016; Van Gosen and Tulsidas, 2016). 

  8. Osteogenic cell cultures cannot utilize exogenous sources of synthetic polyphosphate for mineralization.

    Science.gov (United States)

    Ariganello, Marianne B; Omelon, Sidney; Variola, Fabio; Wazen, Rima M; Moffatt, Pierre; Nanci, Antonio

    2014-12-01

    Phosphate is critical for mineralization and deficiencies in the regulation of free phosphate lead to disease. Inorganic polyphosphates (polyPs) may represent a physiological source of phosphate because they can be hydrolyzed by biological phosphatases. To investigate whether exogenous polyP could be utilized for mineral formation, mineralization was evaluated in two osteogenic cell lines, Saos-2 and MC3T3, expressing different levels of tissue non-specific alkaline phosphatase (tnALP). The role of tnALP was further explored by lentiviral-mediated overexpression in MC3T3 cells. When cells were cultured in the presence of three different phosphate sources, there was a strong mineralization response with β-glycerophosphate (βGP) and orthophosphate (Pi) but none of the cultures sustained mineralization in the presence of polyP (neither chain length 17-Pi nor 42-Pi). Even in the presence of mineralizing levels of phosphate, low concentrations of polyP (50 μM) were sufficient to inhibit mineral formation. Energy-dispersive X-ray spectroscopy confirmed the presence of apatite-like mineral deposits in MC3T3 cultures supplemented with βGP, but not in those with polyP. While von Kossa staining was consistent with the presence or absence of mineral, an unusual Alizarin staining was obtained in polyP-treated MC3T3 cultures. This staining pattern combined with low Ca:P ratios suggests the persistence of Ca-polyP complexes, even with high residual ALP activity. In conclusion, under standard culture conditions, exogenous polyP does not promote mineral deposition. This is not due to a lack of active ALP, and unless conditions that favor significant processing of polyP are achieved, its mineral inhibitory capacity predominates.

  9. Research on the Occurrence of Titanium in Coal-Measure Kaoline in Songyi, Hubei

    Institute of Scientific and Technical Information of China (English)

    Ran Songlin; Shen Shangyue; Cheng Xianzhong

    2004-01-01

    Using X-ray diffraction (XRD) analysis and an electron-probe microanalyser (EPMA), this research found that the main independent mineral of titanium (Ti) in the kaoline of Songyi is anatase. The granularity of anatase is from 0.5 μm to 1.5 μm, and some exceed 10 μm. This research provides important scientific evidence for the exploitation of the coal-measure kaoline in the South China.

  10. Carbon nanotube-based coatings on titanium

    Indian Academy of Sciences (India)

    Elzbieta Dlugon; Wojciech Simka; Aneta Fraczek-Szczypta; Wiktor Niemiec; Jaroslaw Markowski; Marzena Szymanska; Marta Blazewicz

    2015-09-01

    This paper reports results of the modification of titanium surface with multiwalled carbon nanotubes (CNTs). The Ti samples were covered with CNTs via electrophoretic deposition (EPD) process. Prior to EPD process, CNTs were functionalized by chemical treatment. Mechanical, electrochemical and biological properties of CNT-covered Ti samples were studied and compared to those obtained for unmodified titanium surface. Atomic force microscopy was used to investigate the surface topography. To determine micromechanical characteristics of CNT-covered metallic samples indentation tests were conducted. Throughout electrochemical studies were performed in order to characterize the impact of the coating on the corrosion of titanium substrate. In vitro experiments were conducted using the human osteoblast NHOst cell line. CNT layers shielded titanium from corrosion gave the surface-enhanced biointegrative properties. Cells proliferated better on the modified surface in comparison to unmodified titanium. The deposited layer enhanced cell adhesion and spreading as compared to titanium sample.

  11. Effect of size of man-made and natural mineral fibers on chemiluminescent response in human monocyte-derived macrophages.

    OpenAIRE

    2001-01-01

    Fiber size is an important factor in the tumorigenicity of various mineral fibers and asbestos fibers in animal experiments. We examined the time course of the ability to induce lucigenin-dependent chemiluminescence (CL) from human monocyte-derived macrophages exposed to Japan Fibrous Material standard reference samples (glass wool, rock wool, micro glass fiber, two types of refractory ceramic fiber, refractory mullite fiber, potassium titanium whisker, silicon carbide whisker, titanium oxide...

  12. What processes control the oxygen isotopes of soil bio-available phosphate?

    Science.gov (United States)

    Gross, Avner; Angert, Alon

    2015-06-01

    The biological availability of phosphorus (P) is considered to be the limiting factor for plant growth in many natural and agricultural soils. Recent studies demonstrated that valuable information on soil P dynamics can be gained from the stable oxygen isotopes of soil phosphate (δ18OP). However, to interpret this information correctly, our understanding of the processes that controls soil phosphate δ18OP values needs to be improved since most of the current data is based primarily on laboratory studies of pure microbial cultures and enzymatic assays and may not be relevant to soils. Here we designed a series of controlled soil incubation experiments to study the actual isotopic effects induced by abiotic reactions, biological uptake, microbial turnover and organic-P mineralization on soil phosphate δ18OP values. We used this data to estimate the role of these processes in mediating soil P availability. Our study was conducted on Mediterranean soils sampled from the same site during winter, spring and summer. The soils were incubated with various mineral and organic-P compounds and their bioavailable phosphate concentrations and δ18OP values were measured. We confirmed that the role of abiotic reactions on phosphate δ18OP values was negligible and that the δ18OP values of the added phosphate were rapidly driven towards isotopic equilibrium with soil water. We suggest this process was mediated by rapid microbial phosphate turnover. Yet, we did not detect the expected isotopic enrichment effect associated with phosphate biological uptake. In another set of incubation experiments we demonstrated that mineralization of phosphate from organic compounds, such as phospho-mono-ester (PME) and phosphor-di-ester (PDE), produced an offset from isotopic equilibrium, as a result of the strong isotopic fractionation associated with the mineralization process. However, the δ18OP values recorded by the mineralized phosphate were gradually driven back towards isotopic

  13. The role of brushite and octacalcium phosphate in apatite formation.

    Science.gov (United States)

    Johnsson, M S; Nancollas, G H

    1992-01-01

    Studies of apatite mineral formation are complicated by the possibility of forming several calcium phosphate phases. The least soluble, hydroxyapatite (HAP), is preferentially formed under neutral or basic conditions. In more acidic solutions phases such as dicalcium phosphate dihydrate (Brushite, DCPD) and octacalcium phosphate (OCP) are often found. Even under ideal HAP precipitation conditions the precipitates are generally nonstoichiometric, suggesting the formation of calcium-deficient apatites. Both DCPD and OCP have been implicated as possible precursors to the formation of apatite. This may occur by the initial precipitation of DCPD and/or OCP followed by transformation to a more apatitic phase. Although DCPD and OCP are often detected during in vitro crystallization, in vivo studies of bone formation rarely show the presence of these acidic calcium phosphate phases. In the latter case the situation is more complicated, since a large number of ions and molecules are present that can be incorporated into the crystal lattice or adsorbed at the crystallite surfaces. In biological apatite, DCPD and OCP are usually detected only during pathological calcification where the pH is often relatively low. In normal in vivo calcifications these phases have not been found, suggesting the involvement of other precursors or the formation of an initial amorphous calcium phosphate phase (ACP) followed by transformation to apatite.

  14. Biologically Analogous Calcium Phosphate Tubes from a Chemical Garden.

    Science.gov (United States)

    Hughes, Erik A B; Williams, Richard L; Cox, Sophie C; Grover, Liam M

    2017-02-28

    Calcium phosphate (CaPO4) tubes with features comparable to mineralized biological microstructures, such as Haversian canals, were grown from a calcium gel/phosphate solution chemical garden system. A significant difference in gel mass in response to high and low solute phosphate equivalent environments existed within 30 min of solution layering upon gel (p = 0.0067), suggesting that the nature of advective movement between gel and solution is dependent on the solution concentration. The transport of calcium cations (Ca(2+)) and phosphate anions (PO4(3-)) was quantified and changes in pH were monitored to explain the preferential formation of tubes within a PO4(3-) concentration range of 0.5-1.25 M. Ingress from the anionic solution phase into the gel followed by the liberation of Ca(2+) ions from the gel was found to be essential for acquiring self-assembled tubular CaPO4 structures. Tube analysis by scanning electron microscopy (SEM), X-ray diffraction (XRD), and micro X-ray florescence (μ-XRF) revealed hydroxyapatite (HA, Ca10(PO4)6(OH)2) and dicalcium phosphate dihydrate (DCPD, CaHPO4·2H2O) phases organized in a hierarchical manner. Notably, the tubule diameters ranged from 100 to 150 μm, an ideal size for the permeation of vasculature in biological hard tissue.

  15. Interlaboratory comparison of mineral constituents in a sample from the Herrin (No. 6) coal bed from Illinois

    Science.gov (United States)

    Finkelman, Robert B.; Fiene, F.L.; Miller, R.N.; Simon, F.O.

    1984-01-01

    and possibly coquimbite and jarosite were also identified. Scanning electron microscopy studies indicated ubiquitous pyrite framboids and, less commonly, euhedral crystals, skeletal grains, irregularly shaped particles, and vein fillings. Minor accessory minerals such as rare-earth phosphates and possibly silicates, zircon, barium sulfate, titanium oxide, and sphalerite were also found. The textural evidence indicates that the minerals in the banded material are detrital whereas the minerals occurring as vein and pore fillings are authigenic. Magnetic measurements indicate that coal crushed in a steel pulverizer is contaminated by small quantities of abrasion fragments from the crusher, which seriously affect the measured magnetic properties of the coal.

  16. Titanium - ceramic restoration: How to improve the binding between titanium and ceramic

    Directory of Open Access Journals (Sweden)

    Harry Laksono

    2011-03-01

    Full Text Available Background: Titanium alloys has been used as an alternative to nickel-chromium alloys for metal-ceramic restorations because of its good biocompatibility and mechanical properties. This indicated that it was possible to design coping according to standards established for metal-ceramics. However, titanium is chemically reacting strongly with gaseous elements which causes problems when ceramics are fused to titanium. Purpose: To provide information about improving the bonding between titanium and ceramic. Review: Titanium has two crystal modifications, the close-packed hexagonal (α structure, up to 880° C, and above this temperature the bodycentered cubic (β structure. The principal problems is the extensive dissolution of oxygen resulting in thick, oxygen-rich titanium layers called α-case that harms the bonding of ceramic to titanium and the great mismatch in the coefficient of thermal expansion of conventional ultra-low fusing ceramic. Methods have been developed for fusing ceramic to titanium like processing methods, the used of ultra-low fusing titanium ceramic, bonding agent, and protocol for ceramic bonding to titanium. Conclusion: Titanium and titanium alloys, based on their physical and chemical properties suitable for titanium-ceramic restorations, but careful selection of processing methods, ceramic materials, laboratory skill and strict protocol for ceramic bonding to titanium are necessary to improve the bonding between titanium and ceramic.Latar Belakang: Logam campur titanium telah dipakai sebagai salah satu bahan alternatif untuk logam nikel-krom pada pembuatan restorasi keramik taut logam karena mempunyai biokompatibilitas dan sifat mekanik yang baik. Hal ini menunjukkan bahwa logam titanium dapat dipakai untuk pembuatan koping logam berdasarkan standar yang dipakai untuk pembuatan restorasi keramik taut logam. Meskipun, secara kimiawi logam titanium bereaksi dengan elemen-elemen gas yang menyebabkan masalah pada perlekatan

  17. Triphenyl phosphate allergy from spectacle frames

    DEFF Research Database (Denmark)

    Carlsen, L; Andersen, K E; Egsgaard, Helge

    1986-01-01

    A case of triphenyl phosphate allergy from spectacle frames is reported. Patch tests with analytical grade triphenyl phosphate, tri-m-cresyl phosphate, and tri-p-cresyl phosphate in the concentrations 5%, 0.5% and 0.05% pet. showed positive reactions to 0.05% triphenyl phosphate and 0.5% tri-m-cr...

  18. A New Construction Material-Titanium

    Science.gov (United States)

    1974-01-01

    the Academy of Sciences of the Georgian SSR resulted in important proposals for the pro- duction of gallic acid and other preparations. AT-3 tita’ 4um...titanium with various elements, looks at phase transformation in certain alloy systems~and separateI alloys used in Industry. The articles give the...titanium alloys. Questions of the use of titanium and its alloys in various areas of the national econcmy are given. The work was written for scientists

  19. Production of titanium from ilmenite: a review

    Energy Technology Data Exchange (ETDEWEB)

    Kohli, R.

    1981-12-01

    The general principles for beneficiation of titanium ores are reviewed and the specific processes used in individual units in various countries are discussed. This is followed by a critical evaluation of various current and potential reduction methods for the production of titanium metal from the processed concentrates. Finally, the report outlines a research program for the development of a commercially viable alternative method for the production of titanium metal.

  20. Investigation of Infiltrated and Sintered Titanium Carbide

    Science.gov (United States)

    1952-04-01

    taneive investigations in this field during the ’time preceding this contract, and concentrated their effort® On titanium carbide as the’ refractospy...component • The Basic work of this investigation consisted of? X, KpälfiCÄVtloh and refinement of cOmätrcial grades of titanium carbide hj...facilitate a comparison between the different methods» an investigation was then carried out with composite bodies* consisting of titanium carbide asd

  1. Brazing titanium structures. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Pressly, H.B.

    1977-03-01

    A vacuum furnace brazing process using Ag-5A1-0.5Mn brazing alloy has been developed for joining titanium alloy Ti-6Al-4V structures. Lap-shear strengths of the braze joints and the effects of the brazing thermal cycle on the tensile and bending properties of mill-annealed Ti-6Al-4V alloy sheet are reported. Nondestructive test methods were evaluated for detecting defects in these braze joints.

  2. Bioreduction of U(VI) in the presence of phosphate

    Science.gov (United States)

    Boyanov, M. I.; Mishra, B.; Latta, D. E.; Rui, X.; Kwon, M.-J.; Fletcher, K. E.; Loeffler, F. E.; O'Loughlin, E. J.; Kemner, K. M.

    2012-04-01

    Phosphate/phosphoryl moieties are ubiquitous in biological and environmental systems and can potentially affect the speciation of uranium during natural attenuation or stimulated bioremediation processes. The reactivity between U(VI) and phosphate has been studied extensively, but the significant influence of phosphate groups on the formation of reduced U(IV) species has only recently been recognized. We will compare and contrast the bioreduction of dissolved and solid-phase U(VI) by Gram-positive and Gram-negative metal-reducing bacteria (Shewanella, Anaeromyxobacter, Geobacter, and Desulfitobacterium) in the presence and absence of phosphate, from the perspective of solid-phase U speciation as determined by U L-edge x-ray absorption spectroscopy (XANES and EXAFS). In all cases examined, the presence of phosphate at concentrations of P/U > 1 led to the formation of reduced, inner-sphere complexed U(IV)-phosphate species that prevented the lowest-solubility U(IV) mineral uraninite (UO2) from forming over at least several months. In the absence of phosphate, nanoparticulate uraninite or complexed non-uraninite U(IV) species were observed (depending on the system and conditions), suggesting that the interplay between the chemical conditions at the location of electron transfer to U(VI) control the U(IV) product and subsequently the stability of reduced U. The importance of non-uraninite U(IV) species will be discussed in the context of their predominance in biostimulated sediments from the Oak Ridge field site in the United States.

  3. New french uranium mineral species; Nouvelles especes uraniferes francaises

    Energy Technology Data Exchange (ETDEWEB)

    Branche, G.; Chervet, J.; Guillemin, C. [Commissariat a l' Energie Atomique, Lab. du Fort de Chatillon, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1952-07-01

    In this work, the authors study the french new uranium minerals: parsonsite and renardite, hydrated phosphates of lead and uranium; kasolite: silicate hydrated of uranium and lead uranopilite: sulphate of uranium hydrated; bayleyite: carbonate of uranium and of hydrated magnesium; {beta} uranolite: silicate of uranium and of calcium hydrated. For all these minerals, the authors give the crystallographic, optic characters, and the quantitative chemical analyses. On the other hand, the following species, very rare in the french lodgings, didn't permit to do quantitative analyses. These are: the lanthinite: hydrated uranate oxide; the {alpha} uranotile: silicate of uranium and of calcium hydrated; the bassetite: uranium phosphate and of hydrated iron; the hosphuranylite: hydrated uranium phosphate; the becquerelite: hydrated uranium oxide; the curite: oxide of uranium and lead hydrated. Finally, the authors present at the end of this survey a primary mineral: the brannerite, complex of uranium titanate. (author) [French] Dans ce travail, les auteurs etudient les nouveaux mineraux uraniferes francais: parsonsite et renardite, phosphates hydrates de plomb et d'uranium; kasolite: silicate hydrate d'uranium et de plomb uranopilite: sulfate d'uranium hydrate; bayleyite: carbonate d'uranium et de magnesium hydrate; {beta} uranolite: silicate d'uranium et de calcium hydrate. Pour tous ces mineraux, les auteurs donnent les caracteres cristallographiques, optiques, et les analyses chimiques quantitatives. Par contre, les especes suivantes, tres rares dans les gites francais, n'ont pas permis d'effectuer d'analyses quantitatives. Ce sont: l'ianthinite: oxyde uraneux hydrate; l'{alpha} uranotile: silicate d'uranium et de calcium hydrate; le bassetite: phosphate d'uranium et de fer hydrate; la hosphuranylite: phosphate duranium hydrate; la becquerelite: oxyde d'uranium hydrate; la curite: oxyde d

  4. Ion implantation induced nanotopography on titanium and bone cell adhesion

    Energy Technology Data Exchange (ETDEWEB)

    Braceras, Iñigo, E-mail: inigo.braceras@tecnalia.com [Tecnalia, Mikeletegi Pasealekua 2, 20009 Donostia-San Sebastian (Spain); CIBER de Bioingeniería, Biomateriales y Nanomedicina (Ciber-BBN) (Spain); Vera, Carolina; Ayerdi-Izquierdo, Ana [Tecnalia, Mikeletegi Pasealekua 2, 20009 Donostia-San Sebastian (Spain); CIBER de Bioingeniería, Biomateriales y Nanomedicina (Ciber-BBN) (Spain); Muñoz, Roberto [Tecnalia, Mikeletegi Pasealekua 2, 20009 Donostia-San Sebastian (Spain); Lorenzo, Jaione; Alvarez, Noelia [Tecnalia, Mikeletegi Pasealekua 2, 20009 Donostia-San Sebastian (Spain); CIBER de Bioingeniería, Biomateriales y Nanomedicina (Ciber-BBN) (Spain); Maeztu, Miguel Ángel de [Private Practice, P° San Francisco, 43 A-1°, 20400 Tolosa (Spain)

    2014-08-15

    Graphical abstract: Titanium surfaces modified by inert ion implantation affect cell adhesion through modification of the nanotopography in the same dimensional range of that of human bone inorganic phases. - Highlights: • Inert ion implantation on Ti modifies surface nanotopography and bone cell adhesion. • Ion implantation can produce nanostructured surfaces on titanium in the very same range as of those of the mineral phase of the human bone. • Appropriate tool for studying the relevance of nanostructured surfaces on bone mineralization and implant osseointegration. • Ion implantation induced nanotopography have a statistically significant influence on bone cell adhesion. - Abstract: Permanent endo-osseous implants require a fast, reliable and consistent osseointegration, i.e. intimate bonding between bone and implant, so biomechanical loads can be safely transferred. Among the parameters that affect this process, it is widely admitted that implant surface topography, surface energy and composition play an important role. Most surface treatments to improve osseointegration focus on micro-scale features, as few can effectively control the effects of the treatment at nanoscale. On the other hand, ion implantation allows controlling such nanofeatures. This study has investigated the nanotopography of titanium, as induced by different ion implantation surface treatments, its similarity with human bone tissue structure and its effect on human bone cell adhesion, as a first step in the process of osseointegration. The effect of ion implantation treatment parameters such as energy (40–80 keV), fluence (1–2 e17 ion/cm{sup 2}) and ion species (Kr, Ar, Ne and Xe) on the nanotopography of medical grade titanium has been measured and assessed by AFM and contact angle. Then, in vitro tests have been performed to assess the effect of these nanotopographies on osteoblast adhesion. The results have shown that the nanostructure of bone and the studied ion implanted

  5. Effectiveness and cost-efficiency of phosphate binders in hemodialysis

    Directory of Open Access Journals (Sweden)

    Zsifkovits, Johannes

    2009-06-01

    Full Text Available Health political background: In 2006, the prevalence of chronic renal insufficiency in Germany was 91,718, of which 66,508 patients were on dialysis. The tendency is clearly growing. Scientific background: Chronic renal insufficiency results in a disturbance of the mineral balance. It leads to hyperphosphataemia, which is the strongest independent risk factor for mortality in renal patients. Usually, a reduction in the phosphate intake through nutrition and the amount of phosphate filtered out during dialysis are not sufficient to reduce the serum phosphate values to the recommended value. Therefore, phosphate binders are used to bind ingested phosphate in the digestive tract in order to lower the phosphate concentration in the serum. Four different groups of phosphate binders are available: calcium- and aluminium salts are the traditional therapies. Sevelamer and Lanthanum are recent developments on the market. In varying doses, all phosphate binders are able to effectively lower phosphate concentrations. However, drug therapies have achieved recommended