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Sample records for hydrothermally synthesized composite

  1. Hydrothermally synthesized SnO{sub 2}-graphene composites for H{sub 2} sensing at low operating temperature

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    Zhang, Min [College of Science, China University of Petroleum, Qingdao, Shandong 266580 (China); Zhen, Yuhua, E-mail: zhenyh@upc.edu.cn [College of Science, China University of Petroleum, Qingdao, Shandong 266580 (China); Key Laboratory of New Energy Physics & Materials Science in Universities of Shandong, China University of Petroleum, Qingdao, Shandong 266580 (China); Sun, Fuhua; Xu, Chao [College of Science, China University of Petroleum, Qingdao, Shandong 266580 (China)

    2016-07-15

    Graphical abstract: We synthesized the flower-like SnO{sub 2} microspheres and SnO{sub 2}-graphene (S–G) composites with different GN contents through a simple one-pot hydrothermal method. The S–G composite with optimum GN contents exhibits the highest H{sub 2} sensing response of 87.2 at 150 °C, which is about 70 times higher than that of pure SnO{sub 2}. - Highlights: • SnO{sub 2}-graphene (S–G) composites were synthesized by one-pot hydrothermal method. • Compared with pure SnO{sub 2}, S–G composites display much better H{sub 2} sensing performance. • The excellent H{sub 2} sensing performance was obtained at low operating temperature of 150 °C. • H{sub 2} sensing mechanisms of S–G composites have been discussed in view of resistance change. - Abstract: The flower-like SnO{sub 2} and a series of SnO{sub 2}-graphene (S–G) composites have been synthesized through a simple one-pot hydrothermal method. The as-prepared products were characterized by XRD, FESEM, TEM, BET, XPS, and Raman spectroscopy. The results clearly revealed that the three-dimensional flower-like SnO{sub 2} hierarchical structure was destroyed by graphene nanosheets. The possible growth models for flower-like SnO{sub 2} and S–G composites were proposed based on the microstructure characterizations. Furthermore, the H{sub 2} sensing responses of all samples were investigated at low operating temperatures (OT) between 30 and 180 °C. The results indicate that the S–G-2-based sensor exhibits the excellent H{sub 2} sensing response of 87.2 at a relatively low OT of 150 °C, which is about 70 times higher than that of pure SnO{sub 2}. Mechanism of H{sub 2} sensing of S–G composite has been discussed in terms of resistance change, which is influenced by the Schottky barrier at the interface of S–G composites.

  2. Phase composition and morphology of nanoparticles of yttrium orthophosphates synthesized by microwave-hydrothermal treatment: The influence of synthetic conditions

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    Vanetsev, A.S., E-mail: alexander.vanetsev@ut.ee [Institute of Physics, University of Tartu, Ravila 14c, Tartu 50411 (Estonia); Samsonova, E.V. [Institute of Physics, University of Tartu, Ravila 14c, Tartu 50411 (Estonia); Gaitko, O.M. [Kurnakov Institute of General and Inorganic Chemistry RAS, Leninskii Prospekt 31, Moscow 119991 (Russian Federation); Keevend, K. [Institute of Physics, University of Tartu, Ravila 14c, Tartu 50411 (Estonia); Popov, A.V. [Prokhorov General Physics Institute RAS, Vavilov St. 38, Moscow 119991 (Russian Federation); Mäeorg, U. [Institute of Chemistry, University of Tartu, Ravila 14a, Tartu 50411 (Estonia); Mändar, H.; Sildos, I. [Institute of Physics, University of Tartu, Ravila 14c, Tartu 50411 (Estonia); Orlovskii, Yu.V. [Institute of Physics, University of Tartu, Ravila 14c, Tartu 50411 (Estonia); Prokhorov General Physics Institute RAS, Vavilov St. 38, Moscow 119991 (Russian Federation)

    2015-08-05

    Highlights: • We synthesized YPO{sub 4} and YPO{sub 4}⋅0.8H{sub 2}O nanoparticles by microwave-hydrothermal treatment. • We studied “conditions–composition–properties” relations for this synthetic path. • We revealed the mechanism of stabilization of YPO{sub 4}⋅0.8H{sub 2}O phase at high temperatures. - Abstract: Herein we report the study of the influence of synthesis conditions during the microwave-hydrothermal crystallization of freshly precipitated gels on the phase composition and morphology of the rare-earth doped yttrium orthophosphates nanoparticles. We characterize the nanoparticles of YPO{sub 4} and YPO{sub 4}⋅0.8H{sub 2}O using X-ray diffraction analysis, TEM, and FT-IR spectroscopy. Furthermore, we argue that for the given phase the degree of crystallinity and thus the sample morphology depend strongly on the synthesis conditions. We establish that the hexagonal hydrate phase can be obtained by means of microwave-hydrothermal method if one uses phosphate anion excess or adjusts pH of the reaction mixture. Also we show that the metastable hydrate phase is most likely stabilized by hydroxyl groups at elevated temperatures.

  3. Enhanced Photocatalytic Degradation of Methylene Blue Using ZnFe2O4/MWCNT Composite Synthesized by Hydrothermal Method

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    Sonal Singhal

    2013-01-01

    Full Text Available Multiwalled carbon nanotubes (MWCNTs were synthesized using arc discharge method at a magnetic field of 430 G and purified using HNO3/H2O2. Transmission electron micrographs revealed that MWCNTs had inner and outer diameter of ~2 nm and ~4 nm, respectively. Raman spectroscopy confirmed formation of MWCNTs showing G-band at 1577 cm−1. ZnFe2O4 and ZnFe2O4/MWCNT were produced using one step hydrothermal method. Powder X-ray diffraction (XRD confirmed the formation of cubic spinel ZnFe2O4 as well as incorporation of MWCNT into ZnFe2O4. Visible light photocatalytic degradation of methylene blue (MB was studied using pure ZnFe2O4 and ZnFe2O4/MWCNT. The results showed that ZnFe2O4/MWCNT composite had higher photocatalytic activity as compared to pure ZnFe2O4. After irradiation for 5 hours in the visible light, MB was almost 84% degraded in the presence of ZnFe2O4 photocatalyst, while 99% degradation was observed in case of ZnFe2O4/MWCNT composite. This enhancement in the photocatalytic activity of composite may be attributed to the inhibition of recombination of photogenerated charge carriers.

  4. Reduced graphene oxide wrapped ZnS–Ag{sub 2}S ternary composites synthesized via hydrothermal method: Applications in photocatalyst degradation of organic pollutants

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    Amaranatha Reddy, D.; Ma, Rory [Department of Chemistry and Chemical Institute for Functional Materials, Pusan National University, Busan 609-735 (Korea, Republic of); Choi, Myong Yong, E-mail: mychoi@gnu.ac.kr [Department of Chemistry and Research Institute of Natural Sciences, Gyeongsang National University, Jinju 660-701 (Korea, Republic of); Kim, Tae Kyu, E-mail: tkkim@pusan.ac.kr [Department of Chemistry and Chemical Institute for Functional Materials, Pusan National University, Busan 609-735 (Korea, Republic of)

    2015-01-01

    Highlights: • Hydrothermal synthesis of ternary ZnS–Ag{sub 2}S–RGO nanostructures without any additives. • Significant improvement of the photocatalytic activity in RGO wrapped composites. • Near white light emission and stable cycling can lead these composites to find application in near UV-white LEDs and environmental protection issues. - Abstract: In this work, we have successfully synthesized ternary nanohybrid composite, ZnS–Ag{sub 2}S wrapped with reduced graphene oxide (RGO) using hydrothermal method without any surfactant. We have accessed the photocatalytic ability of ZnS–Ag{sub 2}S–RGO nanocomposite using the oxidation of Rhodamine B (RhB) under simulated sunlight irradiation. The superior photocatalytic ability of ZnS–Ag{sub 2}S–RGO compared to bare ZnS, was ascribed to an efficient charge transfer from ZnS to Ag{sub 2}S and graphene sheets. The recyclability results also demonstrated the excellent stability and reliability of the ZnS–Ag{sub 2}S–RGO. In addition to the excellent photocatalytic degradation properties, the synthesized ZnS–Ag{sub 2}S–RGO nanocomposite exhibited near white light emission, which implies that careful design and control of the composition could be lead to find application in near UV-white LEDs. The present work provides new insights into the synthesis and characterizations of ternary ZnS–Ag{sub 2}S–RGO nanocomposites and its wide applications in the environmental protection issues.

  5. [Simultaneous Removal of Cd (II) and Phenol by Titanium Dioxide-Titanate Nanotubes Composite Nanomaterial Synthesized Through Alkaline-Acid Hydrothermal Method].

    Science.gov (United States)

    Lei, Li; Jin, Yin-jia; Wang, Ting; Zhao, Xiao; Yan, You; Liu, Wen

    2015-07-01

    A composite nanomaterial, TiO2/TNTs, was synthesized by TiO2 (P25) through alkaline and acid hydrothermal reaction, which possessed both titanate nanotubes (TNTs) and TiO2 phase. It was found that the adsorption kinetics of Cd(II) onto TiO2/TNTs was very quick, and the adsorption could reach the equilibrium within 30 min. In addition, the maximum adsorption capacity of Cd(II) was as large as 120. 34 mg.g-1 calculated from Langmuir isotherm model. The adsorption mechanism of Cd(II) was ion-exchange between Cd2+ and Na+/H+ located in the interlayers of TNTs. However, the adsorption capacity of phenol on TiO2/TNTs was so small that the photocatalysis for phenol degradation was needed. In the adsorption-photocatalysis system, the removal efficiencies of Cd(II) and phenol could reach up to 99. 6% and 99.7%, respectively. Especially, removal of Cd(II) was attributed to adsorption by TNTs of the composite nanomaterial, while removal of phenol was resulted from photocatalytic reaction by the TiO2 phase. Moreover, the co-existing Cd(II) enhanced the photocatalytic degradation of phenol due to the enhancement on photocatalytic activity of TiO2/TNTs after Cd(II) was adsorbed. Co-existing Na+ did not show obvious effect on the co-removal of Cd(II) and phenol by TiO2/TNTs, but adsorption of Cd(II) was inhibited in the presence of Ca2+ as it could compete for the adsorption sites and enhance the aggregation of the material. Furthermore, TiO2/TNTs could be efficiently reused after desorption via HNO3 and regeneration via NaOH, and the removal efficiencies of Cd(II) and phenol were still as high as 91. 7% and 98. 1% even after three cycles. This study proposed a method to synthesize a material which had both adsorptive and photocatalytic performance, and it was of great importance for application of nanomaterials in the simultaneous removal of heavy metals and organic pollutants.

  6. Spark plasma sintering of hydrothermally synthesized bismuth ferrite

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    Zorica Branković

    2016-12-01

    Full Text Available Bismuth ferrite, BiFeO3 (BFO, powder was synthesized by hydrothermal method from Bi(NO33·5 H2O and Fe(NO33·9 H2O as precursors. The synthesized powder was further sintered using spark plasma sintering (SPS. The sintering conditions were optimized in order to achieve high density, minimal amount of secondary phases and improved ferroelectric and magnetic properties. The optimal structure and properties were achieved after spark plasma sintering at 630 °C for 20 min, under uniaxial pressure of 90 MPa. The composition, microstructure, ferroelectric and magnetic properties of the SPS samples were characterized and compared to those of conventionally sintered ceramics obtained from the same powder. Although the samples sintered using conventional method showed slightly lower amount of secondary phases, the spark plasma sintered samples exhibited favourable microstructure and better ferroelectric properties.

  7. Conductivity dependence on synthesis parameters in hydrothermally synthesized ceria nanoparticles

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    Anis-ur-Rehman, M., E-mail: marehman@comsats.edu.pk; Saleemi, A.S.; Abdullah, A.

    2013-12-05

    Highlights: •Facile synthesis of CeO{sub 2} with composite mediated hydrothermal method is done. •Synthesis parameters significantly effect on conduction. •Enhanced dc electrical conductivity (0.3386 S cm{sup −1}) is observed at 700 °C. •Better ac conductivity is observed 2.661 S cm{sup −1} at 700 °C for 3 MHz. •Potential material for electrolyte in fuel cells for higher efficiencies. -- Abstract: Nanoparticles of cerium oxide were synthesized by Composite Mediated Hydrothermal Approach (CMHA). The synthesis conditions were optimized to enhance the conduction properties and for narrow range of nanocrystallites. The synthesis parameters like hydrothermal treatment temperature (at 180 °C and 220 °C) and time (for 45 min, 70 min and 90 min) were optimized. The structural properties of the prepared ceria were examined by X-ray diffraction (XRD) data. Scherrer’s formula was used to calculate the crystallite sizes of average and most intense peak. Temperature dependent dc conductivity was measured in temperature range 200–700 °C and found to be increasing with the increase in measuring temperature and controlling the other synthesis conditions. The frequency dependent ac conductivity and dielectric properties were measured in frequency range 20 Hz–3 MHz at different temperatures. The ac conductivity increased (from 0.00091 to 2.661 S cm{sup −1}) with the increase in temperature (from 200 to 700 °C). Raman spectrum was observed for the different bands of cerium oxide and oxygen vacancies at 514 nm excitation laser line.

  8. Effect of calcination temperatures on the electrochemical performances of nickel oxide/reduction graphene oxide (NiO/RGO) composites synthesized by hydrothermal method

    Science.gov (United States)

    Chen, Gang; Guan, Hongtao; Dong, Chengjun; Xiao, Xuechun; Wang, Yude

    2016-11-01

    A series of NiO/RGO composites based on NiO nanoparticles anchored on layered RGO surfaces were proposed by the same hydrothermal method combined with different calcination temperatures (250, 300, 400 and 500 °C). The effects of calcination temperatures on the capacitive behaviors have been discussed by investigating the components, morphologies, surface conditions of the NiO/RGO composites. The specific capacitance values of NiO/RGO composites calcined at 250, 300, 400 and 500 °C are 950, 553, 375 and 205 F/g at the current density of 1 A/g and the corresponding capacitance retention are 91.3%, 83.9%, 71.9% and 67.3% after 1000 cycles at the current density of 10 A/g. The results suggest the calcination temperature plays an important role in the electrochemical performances of NiO/RGO composites and the electrochemical performances were deteriorated with the increasing calcination temperatures.

  9. Tailored super magnetic nanoparticles synthesized via template free hydrothermal technique

    Science.gov (United States)

    Attallah, Olivia A.; Girgis, E.; Abdel-Mottaleb, Mohamed M. S. A.

    2016-01-01

    Magnetite nanoparticles of controlled shape and dimensions were synthesized using a modified hydrothermal technique. The influence of different synthesis conditions on the shape, size (length and diameter), structure and magnetic properties of the prepared nanoparticles is presented. The mineral phases, the morphologies, size distribution of the resulting magnetic nanoparticles and their magnetic properties were characterized using different characterization methods. We designed magnetite nanoparticles with different morphologies (nanospheres, nanorods, nanocubes and hexagons) and with improved saturation magnetization reaching 90 emu/g.

  10. Piezoelectric Materials Synthesized by the Hydrothermal Method and Their Applications

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    Takeshi Morita

    2010-12-01

    Full Text Available Synthesis by the hydrothermal method has various advantages, including low reaction temperature, three-dimensional substrate availability, and automatic polarization alignment during the process. In this review, powder synthesis, the fabrication of piezoelectric thin films, and their applications are introduced. A polycrystalline lead zirconate titanate (PZT thin film was applied to a micro ultrasonic motor, and an epitaxial lead titanate (PbTiO3 thin film was estimated as a ferroelectric data storage medium. Ferroelectric and piezoelectric properties were successfully obtained for epitaxial PbTiO3 films. As lead-free piezoelectric powders, KNbO3 and NaNbO3 powders were synthesized by the hydrothermal method and sintered together to form (K,NaNbO3 ceramics, from which reasonable piezoelectric performance was achieved.

  11. Hydrothermally synthesized barium fluoride nanocubes for thermoluminescence dosimetry

    Science.gov (United States)

    Bhadane, Mahesh S.; Dahiwale, S. S.; Bhoraskar, V. N.; Dhole, S. D.

    2016-05-01

    In this work, we report a hydrothermally synthesized Dy doped BaF2 (BaF2:Dy) nanocubes and its Thermoluminescence studies. The synthesized BaF2:Dy samples was found to posses FCC structure and having average size ~ 60-70 nm, as revealed through X-Ray Diffraction. Cubical morphology having size ~90 nm was observed from TEM analysis. The 60Co γ- ray irradiated BaF2:Dy TL dosimetric experiments shows a pre-dominant single glow peak at 153 °C, indicating a single level trap present as a metastable state. Furthermore, BaF2:Dy nanophosphor shows a sharp linear response from 10 Gy to 3 kGy, thus it can be applicable as a gamma dosimeter.

  12. Influence of the surfactant and temperature on the morphology and physical-chemistry properties of hydrothermal synthesized composite oxide BiVO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Yang, T.; Wang, Z.; Yu, C.; Xia, D. [Beijing Univ. of Technology, Beijing (China)

    2007-07-01

    During the past two decades, great advances have been made in photocatalytic field, such as the photocatalytic splitting of water into oxygen and the photocatalytic degradation of organic pollution. The visible light responsive photocatalyst bismuth vanadate (BiVO{sub 4}) exhibits activity toward oxygen separation and 4-alkylphenols oxidation, and is increasingly attractive because approximately half of the solar spectrum is visible light. However, in its three structure systems, tetragonal zircon, monoclinic scheelite and tetragonal scheelite, only the monoclinic scheelite type BiVO{sub 4} has the best photocatalytic ability under visible light irradiation. This paper presented the results of a study that prepared BiVO{sub 4} with monoclinic scheelite structure by adding sodium dodecyl sulfate (SDS) in the solution using hydrothermal methods and examined the factors affecting the particle's grain size, specific area, microstructure, local structure, morphology and its photocatalytic ability. The BiVO{sub 4} samples were characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, ultraviolet-visible spectroscopy and Raman spectroscopy. The photocatalytic activity of the decahedron BiVO{sub 4} was then evaluated under UV and visible light sources. It was concluded that the BiVO{sub 4} prepared in this experiment is a promising photocatalyst to split water into oxygen in the visible light zone. 15 refs., 2 tabs., 6 figs.

  13. Magneto-viscosity of hydrothermal synthesized Cu-Zn ferrite ferrofluids

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    Nisha Gautam

    2017-05-01

    Full Text Available The paraffin based ferrofluids were synthesized using the oleic acid coated Cu-Zn ferrite (CZF nanoparticles of compositions Cu0.6Zn0.4Fe2O4 (CZF1 and Cu0.4Zn0.6Fe2O4 (CZF2 synthesized by hydrothermal process. The transmission electron micrographs (TEM show the cubic shape particles of 4 to 10 nm and 4 to 18 nm size for CZF1 and CZF2 respectively. The nanoparticles show superparamagnetic behaviour. The viscosity increases with increase in magnetic field due to the formation of long chains of magnetic nanoparticles in ferrofluid. At higher flow rate, the magnetic chains break into smaller units and arrange along the flow direction. The flow curves show power law behavior. The size of magnetic nanoparticles influences the magneto-viscosity of the ferrofluids.

  14. Magneto-viscosity of hydrothermal synthesized Cu-Zn ferrite ferrofluids

    Science.gov (United States)

    Gautam, Nisha; Thirupathi, Gadipelly; Singh, Rajender

    2017-05-01

    The paraffin based ferrofluids were synthesized using the oleic acid coated Cu-Zn ferrite (CZF) nanoparticles of compositions Cu0.6Zn0.4Fe2O4 (CZF1) and Cu0.4Zn0.6Fe2O4 (CZF2) synthesized by hydrothermal process. The transmission electron micrographs (TEM) show the cubic shape particles of 4 to 10 nm and 4 to 18 nm size for CZF1 and CZF2 respectively. The nanoparticles show superparamagnetic behaviour. The viscosity increases with increase in magnetic field due to the formation of long chains of magnetic nanoparticles in ferrofluid. At higher flow rate, the magnetic chains break into smaller units and arrange along the flow direction. The flow curves show power law behavior. The size of magnetic nanoparticles influences the magneto-viscosity of the ferrofluids.

  15. PREPARATION OF MULTI-WALLED CARBON NANOTUBES USING NiO CATALYST SYNTHESIZED BY HYDROTHERMAL METHOD

    Institute of Scientific and Technical Information of China (English)

    Y.J. Zhu; Y.L. Chen; X.M. Xue; Y.M. Chen; C.Y. Wu; T.C. Kuang; S.H. Li; H. Y. Zhang

    2003-01-01

    The Ni(OH)2/SiO2 binary colloid was prepared using Ni(NO3)2.6H2O and (C2H5 O)4SiO4 as starting materials and was used to form NiO/SiO2 composite powder by hydrothermal method and desiccant method in open air respectively. Multiwalled carbon nanotubes (MWCNTs) were synthesized respectively by chemical vapor deposition using the NiO/SiO2 catalyst prepared by different methods. The phase and morphology of the catalysts and the morphology, output yield and purity of MWCNTs were compared by XRD, TEM and SEM. The results show that the catalyst powder prepared by hydrothermal method, compared with that by desiccant method, is smaller, better dispersion and has stronger catalytic activity. Pure MWCNTs with smaller tube diameter and narrow range could be obtained at a high yield using that NiO/SiO.2 powder prepared by hydrothermal method as catalyst.

  16. Composites comprising biologically-synthesized nanomaterials

    Science.gov (United States)

    Curran, Seamus; Dias, Sampath; Blau, Werner; Wang, Jun; Oremland, Ronald S; Baesman, Shaun

    2013-04-30

    The present disclosure describes composite materials containing a polymer material and a nanoscale material dispersed in the polymer material. The nanoscale materials may be biologically synthesized, such as tellurium nanorods synthesized by Bacillus selenitireducens. Composite materials of the present disclosure may have optical limiting properties and find use in optical limiting devices.

  17. Photoluminescence and hydrogen gas-sensing properties of titanium dioxide nanostructures synthesized by hydrothermal treatments

    CSIR Research Space (South Africa)

    Sikhwivhilu, LM

    2012-03-01

    Full Text Available -1 ACS Appl. Mater. Interfaces 2012, 4, 1656-1665 dx.doi.org/10.1021/am2018089 Photoluminescence and Hydrogen Gas-Sensing Properties of Titanium Dioxide Nanostructures Synthesized by Hydrothermal Treatments Lucky M. Sikhwivhilu, Siyasanga Mpelane...

  18. Surface Geometry and Chemistry of Hydrothermally Synthesized Single Crystal Thorium Dioxide

    Science.gov (United States)

    2015-03-01

    THORIUM DIOXIDE THESIS Presented to the Faculty Department of Engineering Physics Graduate School of Engineering and Management Air Force...UNLIMITED. AFIT-ENP-MS-15-M-87 SURFACE GEOMETRY AND CHEMISTRY OF HYDROTHERMALLY SYNTHESIZED SINGLE CRYSTAL THORIUM DIOXIDE Scott W. Key...27 10. Process chart for determining geometry and chemistry of ThO2. .............................. 28 11. This AFM

  19. Characterization and adsorption performance of Pb(II) on CuO nanorods synthesized by the hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Arfaoui, Lobna; Kouass, Salah [Laboratoire des matériaux utiles, Institut National de Recherche et d' Analyse Physico-Chimique (INRAP) Sidi Thabet, 2020 Tunis (Tunisia); Dhaouadi, Hassouna, E-mail: dhaouadihassouna@yahoo.fr [Laboratoire Matériaux Traitement et Analyse, Institut National de Recherche et d' Analyse Physico-Chimique (INRAP) Sidi Thabet, 2020 Tunis (Tunisia); Jebali, Raouf [Laboratoire des matériaux utiles, Institut National de Recherche et d' Analyse Physico-Chimique (INRAP) Sidi Thabet, 2020 Tunis (Tunisia); Touati, Fathi [Laboratoire Matériaux Traitement et Analyse, Institut National de Recherche et d' Analyse Physico-Chimique (INRAP) Sidi Thabet, 2020 Tunis (Tunisia)

    2015-10-15

    Highlights: • The nanorods of CuO were synthesized by a hydrothermal route without any surfactant. • X-ray diffraction showed monoclinic structure with space group C{sub 2/c}. • The nanorods show relatively high adsorption capacity for the removal of Pb(II). • The adsorption kinetics could be fitted well by the pseudo-second-order model. • The equilibrium data can be fitted well using the Langmuir isotherm model - Abstract: Copper oxide (CuO) nanorods were synthesized by hydrothermal method. The detailed structural, compositional and optical characterization of this material was also evaluated with XRD, FT-IR, EDS, and UV–vis spectroscopy, which confirmed that the obtained nanorods are well-crystallized CuO and possess good optical properties. SEM and TEM studies revealed that the as-synthesized CuO nanorods are uniform with an average diameter of 17 nm. The adsorption activity of the CuO nanostructures was studied. The adsorption results showed that the CuO nanorods are an effective and efficient adsorbent for the removal of Pb(II) ions. The influence of various operational parameters such as the pH of the solution, the contact time and the initial concentrations were also studied and the results were discussed. The estimated maximum lead ion adsorption capacity of the CuO nanorods was found to be 188.67 mg g{sup −1} at an optimum pH of 6.

  20. A study of thermal properties of sodium titanate nanotubes synthesized by microwave-assisted hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Preda, Silviu, E-mail: predas01@yahoo.co.uk [Institute of Physical Chemistry “Ilie Murgulescu”, 202 Splaiul Independentei, 060021 Bucharest (Romania); Rutar, Melita [Jožef Stefan Institute, Jamova cesta 39, SI-1000 Ljubljana (Slovenia); Jožef Stefan International Postgraduate School, Jamova cesta 39, SI-1000 Ljubljana (Slovenia); Umek, Polona [Jožef Stefan Institute, Jamova cesta 39, SI-1000 Ljubljana (Slovenia); Zaharescu, Maria [Institute of Physical Chemistry “Ilie Murgulescu”, 202 Splaiul Independentei, 060021 Bucharest (Romania)

    2015-11-15

    Highlights: • The microwave-assisted hydrothermal route was used for titanate nanotubes synthesis. • Conversion to single-phase nanotube morphology completes after 8 h reaction time. • The nanotube morphology is stable up to 600 °C, as determined by in-situ XRD and SEM. • Sodium ions migrate to the surface due to thermal motion and structure condensation. - Abstract: Sodium titanate nanotubes (NaTiNTs) were synthesized by microwave-assisted hydrothermal treatment of commercial TiO{sub 2}, at constant temperature (135 °C) and different irradiation times (15 min, 1, 4, 8 and 16 h). The products were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, differential scanning calorimetry and specific surface area measurements. The irradiation time turned out to be the key parameter for morphological control of the material. Nanotubes were observed already after 15 min of microwave irradiation. The analyses of the products irradiated for 8 and 16 h confirm the complete transformation of the starting TiO{sub 2} powder to NaTiNTs. The nanotubes are open ended with multi-wall structures, with the average outer diameter of 8 nm and specific surface area up to 210 m{sup 2}/g. The morphology, surface area and crystal structure of the sodium titanate nanotubes synthesized by microwave-assisted hydrothermal method were similar to those obtained by conventional hydrothermal method.

  1. BIMORPH-TYPE PIEZOELECTRIC THIN FILM BENDING ACTUATORS SYNTHESIZED BY HYDROTHERMAL METHOD

    Institute of Scientific and Technical Information of China (English)

    Du Liqun; Arai Fumihito; Fukuda Toshio; Kwon Guiryong

    2004-01-01

    Lead zirconate titanium solid-solution (PZT) thin films with various thickness are synthesized on titanium substrates by repeated hydrothermal treatments.Young modulus,electric-field- induced displacement and the density of the PZT film are measured respectively.Bimorph- type bending actuators are fabricated using these films.The model,which is used to analyze the driving ability of bimorph-type bending actuators by hydrothermal method,is set up.It can be seen that the driving ability of bimorph-type bending actuators can be greatly improved by optimizing the thickness of PZT thin film and substrate from the theoretical analysis results.The measured values are expected to agree with the theoretical values calculated by the above model.

  2. U and Th Concentration and Isotopic Composition of Hydrothermal Fluids at the Lost City Hydrothermal Field

    Science.gov (United States)

    Ludwig, K. A.; Shen, C.; Cheng, H.; Edwards, R.; Kelley, D. S.; Butterfield, D. A.

    2006-12-01

    Uranium and Th concentration and isotopic composition of hydrothermal fluids at the Lost City Hydrothermal Field (LCHF) were determined using multi-collector inductively coupled plasma mass spectrometry (MC-ICP- MS). The LCHF is an off-axis, serpentinite-hosted hydrothermal system located at 30°N near the Mid- Atlantic Ridge. Carbonate chimneys reaching 60 m in height vent alkaline (pH~10), calcium-rich fluids at 40- 91°C and the towers are home to dense microbial communities. Vent fluid and seawater U and Th concentration and isotopic composition data provide critical information for constraining U-Th chimney ages. The increased sensitivity (1-2%) of MC-ICP-MS combined with an Aridus nebulization system allows the precise measurement of small quantities of sample (~150 ml) with low concentrations (ICP-MS techniques to measure the U and Th concentration and isotopic composition (234U, 238U, 230Th, and 232Th) of eight hydrothermal fluid samples. Endmember fluids with ~1mmol/kg Mg have ~0.02 ng/g U, confirming that end-member fluids contain near-zero values of both Mg and U. Thorium concentrations of fluids are close to deep seawater values. U and Th isotopic compositions are reported at the permil level. These data may provide new insights into the role of serpentinite-hosted hydrothermal systems in the budgets of U and Th in the ocean. Techniques presented in this study may be applied to other hydrothermal and seep environments.

  3. UV-light driven photocatalytic performance of hydrothermally-synthesized hexagonal CePO4 nanorods

    Science.gov (United States)

    Zhu, Zhongqi; Zhang, Ke; Zhao, Heyun; Zhu, Jing

    2017-10-01

    Hexagonal CePO4 nanorods were synthesized via a simple hydrothermal method without the presence of surfactants and then characterized by powder X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), ultraviolet-visible (UV-vis) absorption and photoluminescence (PL) spectroscopy. UV-light driven photocatalytic activities of hexagonal CePO4 nanorods were detailedly demonstrated via degrading different organic dyes such as congo red (CR), organic rhodamine B (RB), methyl orange (MO) and methylene blue (MB) since these nanorods exhibit strong UV absorption with the cutoff edge of about 420 nm.

  4. Photocatalytic properties of hierarchical ZnO flowers synthesized by a sucrose-assisted hydrothermal method

    Science.gov (United States)

    Lv, Wei; Wei, Bo; Xu, Lingling; Zhao, Yan; Gao, Hong; Liu, Jia

    2012-10-01

    In this work, hierarchical ZnO flowers were synthesized via a sucrose-assisted urea hydrothermal method. The thermogravimetric analysis/differential thermal analysis (TGA-DTA) and Fourier transform infrared spectra (FTIR) showed that sucrose acted as a complexing agent in the synthesis process and assisted combustion during annealing. Photocatalytic activity was evaluated using the degradation of organic dye methyl orange. The sucrose added ZnO flowers showed improved activity, which was mainly attributed to the better crystallinity as confirmed by X-ray photoelectron spectroscopy (XPS) analysis. The effect of sucrose amount on photocatalytic activity was also studied.

  5. Photocatalytic degradation of rhodamine B dye using hydrothermally synthesized ZnO

    Indian Academy of Sciences (India)

    K Byrappa; A K Subramani; S Ananda; K M Lokanatha Rai; R Dinesh; M Yoshimura

    2006-10-01

    The sunlight mediated photocatalytic degradation of rhodamine B (RB) dye was studied using hydrothermally prepared ZnO ( = 150°C and ∼ 20–30 bars). Zinc chloride was used as the starting material along with sodium hydroxide as a solvent in the hydrothermal synthesis of ZnO. Different durations were tried to obtain pure ZnO phase, which was later confirmed through powder X-ray diffraction. The photocatalytic behaviour of the prepared ZnO was tested through the degradation of RB. The disappearance of organic molecules follows first-order kinetics. The effect of various parameters such as initial dye concentration, catalyst loading, pH of the medium, temperature of the dye solution, on the photo degradation of RB were investigated. The thermodynamic parameters of the photodegradation of RB, like energy of activation, enthalpy of activation, entropy of activation and free energy of activation revealed the efficiency of the process. An actual textile effluent containing RB as a major constituent along with other dyes and dyeing auxiliaries was treated using hydrothermally synthesized ZnO and the reduction in the chemical oxygen demand (COD) of the treated effluent revealed a complete destruction of the organic molecules along with colour removal.

  6. Flower-like CuO synthesized by CTAB-assisted hydrothermal method

    Indian Academy of Sciences (India)

    Yunling Zou; Yan Li; Nan Zhang; Xiulin Liu

    2011-07-01

    Flower-like CuO nanostructures have been synthesized by cetyltrimethylammonium bromide (CTAB)-assisted hydrothermal method. Here, CuCl2.2H2O was used as copper raw material, and sodium hydroxide was used as precipitate. The resulting CuO powders were characterized by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). X-ray diffraction (XRD) pattern exhibited the nanocrystalline nature with monoclinic structure for the as-synthesized nanostructures. FESEM images indicated that the flower-like CuO nanostructures are composed of many interconnected nanosheets in size of several micrometres in length and width and 60–80 nm in thickness. The possible formation mechanism of flower-like CuO nanostructures was discussed.

  7. Influence of Heat Treatment on Photocatalytic Performance of BiVO4 Synthesized by Hydrothermal Method

    Science.gov (United States)

    Shen, Yi; Wang, Xiaomin; Zuo, Guifu; Li, Fengfeng; Meng, Yanzhi

    2016-10-01

    Monoclinic BiVO4 photocatalyst was successfully synthesized by hydrothermal method under appropriate temperature. The photocatalytic performance of BiVO4 was improved by calcining at appropriate temperature. The structural and morphological properties of the synthesized BiVO4 photocatalysts were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. It is confirmed that the photocatalytic activity of the prepared catalysts was evaluated by the photodegradation of RhB under visible-light irradiation. BiVO4 calcined under appropriate temperature exhibited higher photocatalytic activity than uncalcined BiVO4 under visible light irradiation because calcination might effectively increases the purity of monoclinic bismuth vanadate.

  8. Dynamic formation of zeolite synthesized from fly ash by alkaline hydrothermal conversion.

    Science.gov (United States)

    Zhang, ZhiJian; Li, Jiangli; Li, Hongyi; Wang, Hang; Zhu, Jun; He, Qiang

    2013-11-01

    This study was designed to characterize the dynamic formation of zeolite synthesized from fly ash (ZFA) and to identify the zeolitization mechanisms during a 160-h-long hydrothermal alkaline conversion at 95°C by using fly ash (FA) samples collected from four typical thermoelectric power plants in China, with the purpose of improving ZFA quality. The process of synthesizing ZFA can be fundamentally divided into five stages: induction stage (0-0.5 h), accelerating dissolution stage (0.5-12 h), nucleation and/or crystallization stage (12-24 h), crystal growth stage (24-72 h) and crystal transformation stage (72-160 h). The crystal growth stage determined the quality of zeolite crystallization, coupled with functions of re-assembling the silicon-aluminium tetrahedral network and developing submicro- and/or nanometer microstructure. A 48-h-long hydrothermal conversion generated ZFAs that had a greater specific surface area (26.0-89.4 times) and cation exchange capacity (29.6-71.0 times) than FA, which successfully sequestrated 41-95% of ammonium and 75-98% of phosphate from swine manure. However, over-reaction resulted in more stable hydroxysodalite and/or sodalite, surface agglomeration and cracking, and energy wasting. This work suggests that the reuse of recycled synthesis materials should occur during the fourth step (24-72 h).

  9. Morphology and phase transformations of tin oxide nanostructures synthesized by the hydrothermal method in the presence of dicarboxylic acids

    Science.gov (United States)

    Zima, Tatyana.; Bataev, Ivan

    2016-11-01

    A new approach to the synthesis of non-stoichiometric tin oxide structures with different morphologies and the phase compositions has been evaluated. The nanostructures were synthesized by hydrothermal treatment of the mixtures of dicarboxylic acids ― aminoterephthalic or oxalic ― with nanocrystalline SnO2 powder, which was obtained via the sol-gel technology. The products were characterized by Raman and IR spectroscopy, SEM, HRTEM, and XRD analysis. It was shown that the controlled addition of a dicarboxylic acid leads not only to a change in the morphology of the nanostructures, but also to SnO2-SnO2/Sn3O4-Sn3O4-SnO phase transformations. A single-phase Sn3O4 in the form of the well-separated hexagonal nanoplates and mixed SnO2/Sn3O4 phases in the form of hierarchical flower-like structures were obtained in the presence of organic additives. The effects of concentration, redox activity of the acids and heat treatment on the basic characteristics of the synthesized tin oxide nanostructures and phase transformations in the synthesized materials are discussed.

  10. Humidity-Sensing Properties of One-Step Hydrothermally Synthesized Tin Dioxide-Decorated Graphene Nanocomposite on Polyimide Substrate

    Science.gov (United States)

    Zhang, Dongzhi; Chang, Hongyan; Liu, Runhua

    2016-08-01

    This paper demonstrates the one-step hydrothermal synthesis of a tin dioxide (SnO2)-decorated reduced graphene oxide (RGO) hybrid nanocomposite, which was drop-casted on a polyimide substrate as a humidity sensor. The as-synthesized hybrid was characterized in terms of its nanostructural, morphological and compositional features by SEM, XRD and nitrogen sorption. The humidity sensing properties of the presented RGO/SnO2 hybrid nanocomposite, such as repeatability, stability, response-recovery characteristics, were investigated by exposing it to a broad humidity range of 11-97% RH at room temperature. As a result, the sensor demonstrated a high sensitivity, a good repeatability, an acceptable linearity, a fast response/recovery characteristic and high long-term stability over a full humidity range measurement, indicating the unique advantages of one-step hydrothermal synthesis for sensor fabrication. The possible and proposed sensing mechanism for the sensor is mainly attributed to a humidity-induced transfer of charge carriers occuring at the interfaces and the swelling effect of RGO.

  11. Photoluminescence properties of PZT 52/48 synthesized by microwave hydrothermal method using PVA with template

    Energy Technology Data Exchange (ETDEWEB)

    Teixeira, G.F., E-mail: guilmina@hotmail.com [Instituto de Quimica, Universidade Estadual Paulista, Departamento de Bioquimica e Tecnologia Quimica, Rua Francisco Degni s/n, Quitandinha, 14800-900 Araraquara, SP (Brazil); Gasparotto, G. [Instituto de Quimica, Universidade Estadual Paulista, Departamento de Bioquimica e Tecnologia Quimica, Rua Francisco Degni s/n, Quitandinha, 14800-900 Araraquara, SP (Brazil); Paris, E.C. [Empresa Brasileira de Pesquisa Agropecuaria, Embrapa Instrumentacao, Rua XV de novembro, 1452, Centro, 13.569-970 Sao Carlos, SP (Brazil); Zaghete, M.A.; Longo, E.; Varela, J.A. [Instituto de Quimica, Universidade Estadual Paulista, Departamento de Bioquimica e Tecnologia Quimica, Rua Francisco Degni s/n, Quitandinha, 14800-900 Araraquara, SP (Brazil)

    2012-01-15

    Lead Titanate Zirconate (PZT) perovskite powders were synthesized by microwave hydrothermal method (M-H) at 180 {sup o}C for different time periods (2, 4, 8 and 12 h) with the presence of aqueous polyvinyl alcohol (PVA) solution 0.36 g L{sup -1}. The X-Ray diffraction (XRD), SE-FEG as well as the measurements of photoluminescence (PL) emission were used for monitoring the formation of a perovskite phase with random polycrystalline distortion in the structure. Emission spectra with fixed excitation wavelength of 350 nm showed higher value for the powder obtained after undergoing 8 h of treatment. A theoretical model derived from previous calculations allows us to discuss the origin of photoluminescence emission in the powders, which can be further related to the local disorder in the network of both ZrO{sub 6} and TiO{sub 6} octahedral, and dodecahedral PbO{sub 12}. The new morphology initially observed from the PZT perovskite crystal growth bearing the shape of fine plates is found to be directly related to photoluminescence emission with energy lower than that present in the PZT with cube-like morphology that emits in 560 nm. - Highlights: > This work details the efficiency of microwave hydrothermal synthesis in obtaining PZT powders. > PVA is used as a crystallization agent of PZT particles. > PZT particles presented photoluminescent (PL) behavior. > There aren't previous reports of photoluminescent PZT obtained by microwave hydrothermal synthesis. > Photoluminescence is one more interesting property for technological applications this material.

  12. Synthesis of dittmarite/Mg(OH){sub 2} composite coating on AZ31 using hydrothermal treatment

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Qing, E-mail: qzhaoyuping@bit.edu.cn; Mahmood, Waqas; Zhu, Yanying

    2016-03-30

    Highlights: • Synthesis of dittmarite Mg(OH){sub 2} coating on AZ31 alloy by hydrothermal method. • The mechanism of composite coating growth and its characterizations. • The coating is corrosion resistant significantly. • Lack of hydroxyl deposition on the coating surface. • Strong adhesion between the coating and the substrate. • The synthesized coating meets the cytotoxicity standards. - Abstract: In this work, we have used hydrothermal method for the synthesis of dittmarite/Mg(OH){sub 2} composite (DMC) layer on AZ31 alloy of magnesium. The synthesized coating was characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and energy dispersive X-ray spectroscopy (EDS). In a test immersion into the Hank's mixture for 31 days, the synthesized coating inhibited corrosion of AZ31 significantly and the amorphous calcium apatite precursor deposited on the coating surface. In another tape test, we noticed strong adhesion between the coating and substrate that eventually concludes that the synthesized coating is hydrophilic and a promising candidate to be used in the absorbable implant materials. Besides, the cytotoxicity of the AZ31 alloy with DMC coating, grown under different conditions on L-929 cells in vitro was examined indirectly through the growth inhibition method (MTT assay). The cytotoxicity of the deposited coating lie between 0 ∼ 1 that indicates it as a promising biomaterial.

  13. Effects of La3+ doping on MnZn ferrite nanoscale particles synthesized by hydrothermal method

    Institute of Scientific and Technical Information of China (English)

    古映莹; 谭小平; 梁叔全; 桑商斌

    2004-01-01

    MnZn ferrite nanoscale particles were synthesized by hydrothermal method. The effects of amount of addition La3+ on the products were discussed. The product was characterized by X-ray diffraction (XRD) and transmission electron microscope (TEM). The results show that the sample with 0.2% La3+(mass fraction) or without La3+ has only spinel phase, but the sample with mass fraction of La3+ exceeding 0.4% posses second phase besides the spinel one; and the nano-MnZn ferrites change from cube to hexagon when the mass fractions of La3+ is up to 1.2%. TEM image of the sample with 1.2% La3+ indicates that the homogeneous hexagonal crystal is obtained and the particles are larger than those of undoped; the addition of La3+ has great influence on the crystallization of hydrothermal process and can change the shape of particles and improve their growth. The saturation magnetization of the sample with 1.2% La3+ (2.64 A·m2·kg-1) is lower than that of undoped (17.54 A·m2·kg-1) and it behaves superparamagnetically.

  14. Field-emission stability of hydrothermally synthesized aluminum-doped zinc oxide nanostructures.

    Science.gov (United States)

    Hsieh, Tsang-Yen; Wang, Jyh-Liang; Yang, Po-Yu; Hwang, Chuan-Chou; Shye, Der-Chi

    2012-07-01

    The Al-doped ZnO (AZO) nanostructures field-emission arrays (FEAs) were hydrothermally synthesized on AZO/glass substrate. The samples with Al-dosage of 3 at.% show the morphology as nanowires vertically grown on the substrates and a structure of c-axis elongated single-crystalline wurtzite. The good field-emission (i.e., the large anode current and low fluctuation of 15.9%) can be found by AZO nanostructure FEAs with well-designed Al-dosage (i.e., 3 at.%) because of the vertical nanowires with the less structural defects and superior crystallinity. Moreover, the Full width at half maximum (FWHM) of near band-edge emission (NBE) decreased as the increase of annealing temperature, representing the compensated structural defects during oxygen ambient annealing. After the oxygen annealing at 500 degrees C, the hydrothermal AZO nanostructure FEAs revealed the excellent electrical characteristics (i.e., the larger anode current and uniform distribution of induced fluorescence) and enhanced field-emission stability (i.e., the lowest current fluctuation of 5.97%).

  15. Red luminescence from hydrothermally synthesized Eu-doped ZnO nanoparticles under visible excitation

    Indian Academy of Sciences (India)

    P M Aneesh; M K Jayaraj

    2010-06-01

    Eu-doped ZnO nanoparticles were synthesized by hydrothermal method. The Eu-dopant concentration has been varied by varying the amount of Eu-dopant concentration. These nanoparticles were structurally characterized by X-ray diffraction, transmission electron microscopy and selected area electron diffraction and it confirms the formation of nanoparticles having standard wurtzite structure. Photoluminescence studies show that these nanoparticles exhibit a sharp red luminescence due to the intra-4 transitions of Eu3+ ions at an excitation of 397 nm and 466 nm. Luminescence quenching is observed in the nanoparticles as the Eu-dopant concentration increases. Incorporation of Eu in the nanoparticles was confirmed by the energy dispersive X-ray studies.

  16. Ion beam analysis of zeolites type Li-ABW synthesized by hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Andrade, E.; De Lucio, O. G.; Solis, C.; Zavala, E. P.; Cruz, J. [UNAM, Instituto de Fisica, Circuito Exterior, Ciudad Universitaria, 04510 Mexico D. F. (Mexico); Alfaro, S.; Rodriguez, C.; Valenzuela, M. A. [IPN, Escuela Superior de Ingenieria Quimica e Industrias Extractivas, Laboratorio de Catalisis y Materiales, Zacantenco, 07738 Mexico D. F. (Mexico); Rocha, M. F. [IPN, Escuela Superior de Ingenieria Mecanica y Electrica, Av. Instituto Politecnico Nacional s/n, Col. Lindavista, 07738 Mexico D. F. (Mexico); Murillo, G.; Policroniades, R. [ININ, Carretera Mexico-Toluca s/n, Ocoyoacac 52750, Estado de Mexico (Mexico)

    2010-02-15

    This work reports a method to synthesize and characterize Li-ABW zeolites by a hydrothermal method. These materials are good candidates for CO{sub 2} capture because of the high reactivity between the Li{sup +} with CO{sub 2} to form Li{sub 2}CO{sub 3}. We performed and elemental profile concentration using ion beam analysis. The elastic backscattered proton energy spectra from the Al, Si, O and Li nuclei, in combination with the {alpha} particles from the {sup 7}Li ({rho}, {alpha}){sup 4}He nuclear reaction energy spectra, were employed for this task. X-ray diffraction was also applied to determine the crystalline structure. (Author)

  17. The gas sensing properties of TiO2 nanotubes synthesized by hydrothermal method

    Institute of Scientific and Technical Information of China (English)

    Yan Li Wang; Shun Tan; Jia Wang; Zhi Jin Tan; Qiu Xia Wu; Zheng Jiao; Ming Hong Wu

    2011-01-01

    In this paper, the TiO2 nanotubes were synthesized by hydrothermal method usinga 10 mol/LNaOH aqueous solution at 150 ℃. The structure of prepared materials was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscope (SEM) and Brunauer-Emmett-Teller (BET). The prepared TiO2 nanotubes were used to prepare thick film gas sensors and the gas sensing properties to various gases were tested. Results show the prepared TiO2 nanotube gas sensors responses to ethanol under dry condition at 450 ℃. This could be attributed to the fact that it had high porous morphology and a higher pore volume, which can promote the diffusion of ethanol deep inside the films and improve the sensor response. Moreover, the gas sensor made with nanotubes exhibit high selective response towards ethanol gas compared with H2, CO, acetone.

  18. Biocompatibility and antimicrobial activity of zinc(II doped hydroxyapatite, synthesized by hydrothermal method

    Directory of Open Access Journals (Sweden)

    Kojić Vesna

    2012-01-01

    Full Text Available In order to obtain multifunctional materials with good biocompatibility and antimicrobial effect, hydroxyapatite (HAp doped with Zn2+ was synthesized by hydrothermal method. Powders with different content of zinc ions were synthesized and compared with undoped HAp to investigation of Zn2+ ion influence on the antimicrobial activity of HAp. Analyses of undoped and Zn2+-doped powders before and after thermal treatment at 1200ºC were performed by SEM and XRD. Antimicrobial effects of powders were examined in relation to Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa and Candida albicans in liquid medium. The results showed that the obtained powders have good antimicrobial activity, but higher antimicrobial activities of powders doped with Zn2+ were observed after annealing at 1200°C. For powders annealed at 1200°C in vitro biocompatibility tests MTT and DET with MRC-5 fibroblast cells in liquid medium were carried out. Based on MTT and DET tests it was shown that powders do not have a significant cytotoxic effect, which was confirmed by SEM analysis of MRC-5 fibroblast cells after theirs in vitro contact with powders. [Projekat Ministarstva nauke Republike Srbije, br. III 45019 and FP7-REGPOT-2009-1 NANOTECH FTM

  19. Magnetic properties of hydrothermally synthesized greigite (Fe3S4)- II. High- and low-temperature characteristics

    NARCIS (Netherlands)

    Dekkers, M.J.; Passier, Hilde F.; Schoonen, M.A.A.

    1999-01-01

    The magnetic behaviour of hydrothermally synthesized greigite was analysed in the temperature range from 4 K to 700 °C. Below room temperature, hysteresis parameters were determined as a function of temperature, with emphasis on the temperature range below 50 K. Saturation magnetization and initial

  20. Au-controlled enhancement of photoluminescence of NiS nanostructures synthesized via a microwave-assisted hydrothermal technique

    CSIR Research Space (South Africa)

    Linganiso, EC

    2014-11-01

    Full Text Available Nickel sulphide (NiS) nanostructures decorated with gold (Au) nanoparticles (NPs) were synthesized via a microwave-assisted hydrothermal technique. Binary phase NiS (a and ß) crystalline nanostructures, bare, and decorated with Au NPs were obtained...

  1. Effect of Amino Acids on Morphology of Hydrothermally Synthesized Hydroxyapatite Fibers

    Directory of Open Access Journals (Sweden)

    QI Mei-li

    2017-05-01

    Full Text Available Based on the basic principle of biomineralization, hydroxyapatite fiber (HAF with high crystallinity was fabricated via a hydrothermal route with Ca(NO32·4H2O and (NH42HPO4 as the resources, respectively. Effects of the addition of acidic amino acid L-glutamic acid (Glu, neutral amino acid L-phenylalanine (Phe and basic amino acid L-lysine (Lys on the phase composition and morphology of the obtained products were laid special emphasis on. The results show that the products obtained by using the three amino acids are all hydroxyapatite (HA phase with minor CaCO3 in some samples. Meanwhile, all of the amino acids inhibit the growth of the fibers. Spherical morphology exists when Glu is added, the homogeneity of the fibers deteriorates with the addition of Lys. However, rod-like fibers with good uniformity can be obtained with the addition of Phe.

  2. Synthesizing Smart Polymeric and Composite Materials

    OpenAIRE

    2013-01-01

    Smart materials have been widely investigated to explore new functionalities unavailable to traditional materials or to mimic the multifunctionality of biological systems. Synthetic polymers are particularly attractive as they already possess some of the attributes required for smart materials, and there are vast room to further enhance the existing properties or impart new properties by polymer synthesis or composite formulation. In this work, three types of smart polymer and composites have...

  3. Microstructure, morphology and magnetic properties of Ni nanoparticles synthesized by hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Bouremana, A. [LPM, Faculty of Sciences, USTHB, BP 32, El-Alia, Bab Ezzouar, Algiers (Algeria); Guittoum, A., E-mail: aguittoum@gmail.com [Nuclear Research Centre of Algiers, 02 Bd Frantz Fanon, BP 399, Alger-Gare, Algiers (Algeria); Hemmous, M. [Nuclear Research Centre of Algiers, 02 Bd Frantz Fanon, BP 399, Alger-Gare, Algiers (Algeria); Martínez-Blanco, D. [SCTs, University of Oviedo, EPM, 33600 Mieres (Spain); Gorria, Pedro [Department of Physics & IUTA, EPI, University of Oviedo, 33203 Gijón (Spain); Blanco, J.A. [Department of Physics, University of Oviedo, Calvo Sotelo St., 33007 Oviedo (Spain); Benrekaa, N. [LPM, Faculty of Sciences, USTHB, BP 32, El-Alia, Bab Ezzouar, Algiers (Algeria)

    2015-06-15

    Powder samples containing high purity nickel nanoparticles (NPs) were prepared by hydrothermal method from Ni(II) chloride hexahydrate (NiCl{sub 2}·6H{sub 2}O) under the presence of sodium hydroxide (NaOH) with different concentrations between 5 and 25 mol/L. The synthesis of the NPs occurs through chemical reduction at relatively low temperature (140 °C). The Ni NPs have a face-centred cubic (fcc) crystal structure with a lattice parameter value close to that of pure Ni (a = 3.52 Å). The average crystallite size determined from x-ray diffraction is around 20 nm, except for the sample synthesized under the highest NaOH concentration (25 mol/L), which has the largest average size (>30 nm). The powder morphology at the sub-micrometre length scale looks like agglomerates of Ni-NPs that drastically changes their shape depending on the NaOH concentration, from flower (5 mol/L) to a dendritic-like (25 mol/L). All the samples are ferromagnetic at room temperature with saturation magnetization values between 50 and 52emu/g, and a coercive field that increases with the NaOH concentration from around 135 (5 mol/L) up to 180Oe (25 mol/L). - Highlights: • Pure Nickel nanoparticles have been synthesized by a chemical reaction process. • Different morphologies were observed with the change of NaOH concentration. • The coercive field increases with increasing the NaOH concentration and depends on the shape of nanoparticles.

  4. Electrochemical Performance of Morphologically Different Bi2WO6 Nanostructures Synthesized via a Hydrothermal Route

    Science.gov (United States)

    Wang, Fei; Yang, Hua; Zhang, Haimin; Su, Junyan; Wang, Xiangxian

    2017-01-01

    Morphologically different Bi2WO6 nanostructures have been synthesized via a hydrothermal route, where the morphology was tailored by varying the pH value of the precursor solution. The samples prepared at pH 1, 7, and 11 consisted of flower-like hierarchical structures with average diameter of 7 μm, irregular flake-like structures with average thickness of 90 nm, and uniform spherical structures with average size of 85 nm, respectively. The electrochemical performance of the as-prepared Bi2WO6 samples was investigated by cyclic voltammetry, galvanostatic charge-discharge measurements, and electrochemical impedance spectroscopy. In 1 M KOH electrolyte at current density of 0.5 mA cm-2, the specific capacitance of the Bi2WO6 with flower-like hierarchical, flake-like, and spherical structure was measured to be 255 F g-1, 214 F g-1, and 412 F g-1, respectively. After 850 charge-discharge cycles at current density of 3 mA cm-2, the capacitance of the three samples remained at 87%, 78%, and 95% of the initial value, respectively. Among the three types of Bi2WO6 morphology, the spherical structure delivered the best electrochemical performance.

  5. Preparation of Nanosized LaCoO3 through Calcination of a Hydrothermally Synthesized Precursor

    Directory of Open Access Journals (Sweden)

    L. Tepech-Carrillo

    2016-01-01

    Full Text Available A method for obtaining nanosized LaCoO3 crystals from calcination of a precursor powder synthesized by a hydrothermal route is reported. Details concerning the evolution of the microstructure and formation mechanism of the perovskite phase were studied by powder X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, Raman spectroscopy, and thermal analysis. It was found that the morphology of the sample progressively turns from a mix of fibers and rods to interconnected nanocrystals. It is determined that LaCoO3 phase is produced by a reaction of cobalt and lanthanum oxides, the latter produced by a two-step dehydration process of La(OH3. Finally, it was found that nearly stoichiometric LaCoO3 nanocrystals can be obtained at temperatures as low as 850°C. Nevertheless, whether higher calcination temperatures are used, appropriate reaction times and a controlled atmosphere are required in order to avoid formation of lanthanum carbonates and high density of lattice defects.

  6. Sulfur isotopic composition of modern seafloor hydrothermal sediment and its geological significance

    Institute of Scientific and Technical Information of China (English)

    曾志刚; 李军; 蒋富清; 秦蕴珊; 翟世奎

    2002-01-01

    A total of 1 264 sulfur isotopic values for modem seafloor hydrothermel sediments from different hydrothermal fidds have been collected. On this basis, combining our sulfur isotpic data for surface hydrothermal sediments from the Jade hydrohtermal field in the Okinawa Trough and the TAG hydrothermal field in the Mid-Atlantic Ridge, respectively, and comparing the sulfur isotopic compositions and analyzing their sources of sulfur in seafloor hydrothermal sediments from different geologic-tectonic setting, the results show that: ( 1 ) sulfur isotopic values of sulfides and sulfates in modern seafloor hydrothermal sediments are concentrated in a narrow range, δ34S values of sulfides vary from l × 10-3 to 9 × 10- 3, with a mean of 4.5 × 10- 3 ( n = 1 042), δ34S values of sulfates vary from 19 × 10- 3 to 24× 10-3, with a mean of 21.3× 10-3 (n =217); (2) comparing the sulfur isotopic compositions of hydrothermal sediments from the sediment-hosted hydrothermal fields, the range of sulfur isotopic values for hydrothermal sediments from the sediment-free hydrothermal fields is narrow relatively; (3) the differences of sulfur isotopic compositions in sulfides from different hydrothermal fields show the differences in the sources of sulfur. The sulfur of hydrothermal sulfides in the sediment-free mid-ocean ridges is mainly from mid-ocean ridge basalt, and partially from the reduced seawater sulfate, and it is the result of partially reduced seawater sulfate mixed with basaltic sulfur. In the sediment-hosted nid-ocean ridges and the back-arc basins, the volcanics, the sediments and the organic matters also can offer their sulfur for forming hydrothermal sulfides; (4) the variations of sulfur isotopic compositions and the different sources of sulfur for hydrothermal sediments may be attributed to the various physical-chemical characteristics of hydrothermal fluids, the magmatic evolution and the different geologic-tectonic settings of seafloor hydrothermal systems.

  7. Selective oxidation of propylene to acrolein by hydrothermally synthesized bismuth molybdates

    DEFF Research Database (Denmark)

    Schuh, Kirsten; Kleist, Wolfgang; Høj, Martin

    2014-01-01

    Hydrothermal synthesis has been used as a soft chemical method to prepare bismuth molybdate catalysts for the selective oxidation of propylene to acrolein. All obtained samples displayed a plate-like morphology, but their individual aspect ratios varied with the hydrothermal synthesis conditions...

  8. Thermoelectric properties of Ag2 S/Bi2 S3 composite synthesized by hydrothermal method%水热法合成Ag2 S/Bi2 S3复合材料及其热电性能研究∗

    Institute of Scientific and Technical Information of China (English)

    罗世阶; 鲜聪; 王伟; 谢淑红; 陈秋帆; 闫艳慈; 周小元

    2016-01-01

    Ag2 S/Bi2 S3 composite powders with spherical structure was synthesized successfully by hydrothermal method and then pressed into bulk by spark plasma sintering technique.The crystalline structure and morpholo-gy of the powder was determined by X-ray diffraction and scanning electron microscopy.The effect of Ag2 S con-tent on the Ag2 S/Bi2 S3 composite thermoelectric properties was investigated systematically.The thermoelectric performance results showed that the Seebeck coefficients of all the Ag2 S/Bi2 S3 samples were negative,which in-dicated that the composites were n-type semiconductors.Appropriate Ag2 S added in Bi2 S3 could not only reduce the thermal conductivity,but also enhanced the electrical conductivity.The maximal ZT of Bi2 S3 with 3% Ag2 S was 0.29 at 724 K,which is twice than that of the pure Bi2 S3 .%采用水热合成法结合放电等离子烧结技术制备了Ag2 S/Bi2 S3块体热电复合材料.采用XRD、SEM和TEM对合成粉末材料的相组成和微观形貌进行分析,闪光法和塞贝克系数/电阻测量系统测试复合块材的热电性能,系统地研究了Ag2 S的含量对Ag2 S/Bi2 S3复合材料热电性能的影响.实验结果表明,水热法成功地合成了具有球形结构的Ag2 S/Bi2 S3复合粉末;块体样品的塞贝克系数都为负,说明样品为 n型半导体;适量的 Ag2 S 复合Bi2 S3不仅有效地降低了材料的热导率,同时也提高了电导率;当Bi2 S3与3%的 Ag2 S复合时样品的热电优值(ZT 值)最大,其在724 K时的ZT 值为0.23,为纯Bi2 S3样品在该温度ZT 值的2.3倍.

  9. Two-step hydrothermal synthesis of Ru-Sn oxide composites for electrochemical supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Chi-Chang; Chang, Kuo-Hsin; Wang, Chen-Ching [Department of Chemical Engineering, National Chung Cheng University, Chia-Yi 621 (China)

    2007-03-20

    A two-step hydrothermal process was developed to synthesize hydrous 30RuO{sub 2}-70SnO{sub 2} composites with much better capacitive performances than those fabricated through the normal hydrothermal process, co-annealing method, or modified sol-gel procedure. A very high specific capacitance of RuO{sub 2} (C{sub S,Ru}), ca. 1150 F g{sup -1}, was obtained when this composite was synthesized via this two-step hydrothermal process with annealing in air at 150 C for 2 h. The voltammetric currents of this annealed composite were found to be quasi-linearly proportional to the scan rate of CV (up to 500 mV s{sup -1}), demonstrating its excellent power property. From Raman, UV-vis spectroscopic and TEM analyses, the reduction in mean particulate size is clearly found for this two-step oxide composite, attributable to the co-precipitation of (Ru{sub {delta}}Sn{sub 1-{delta}})O{sub 2}.xH{sub 2}O onto partially dissolved SnO{sub 2}.xH{sub 2}O and the formation of (Ru{sub {delta}}Sn{sub 1-{delta}})O{sub 2}.xH{sub 2}O crystallites in the second step. This effect significantly promotes the utilization of RuO{sub 2} (i.e., very high C{sub S,Ru}). The excellent capacitive performances, very similar to that of RuO{sub 2}.xH{sub 2}O, suggest the deposition of RuO{sub 2}-enriched (Ru{sub {delta}}Sn{sub 1-{delta}})O{sub 2}.xH{sub 2}O onto SnO{sub 2}.xH{sub 2}O seeds as well as the individual formation of (Ru{sub {delta}}Sn{sub 1-{delta}})O{sub 2}.xH{sub 2}O crystallites in the second hydrothermal step. (author)

  10. Hydrothermal syntheses and characterization of uranyl tungstates with electro-neutral structural units

    Energy Technology Data Exchange (ETDEWEB)

    Balboni, Enrica; Burns, Peter C. [Univ. of Notre Dame, IN (United States). Dept. of Civil and Enviromental Engineering and Earth Sciences; Univ. of Notre Dame, IN (United States). Dept. of Chemistry and Biochemistry

    2015-11-01

    Two uranyl tungstates, (UO{sub 2})(W{sub 2}O{sub 7})(H{sub 2}O){sub 3} (1) and (UO{sub 2}){sub 3}(W{sub 2}O{sub 8})F{sub 2}(H{sub 2}O){sub 3} (2), were synthesized under hydrothermal conditions at 220 C and were structurally, chemically, and spectroscopically characterized. 1 Crystallizes in space group Pbcm, a = 6.673(5) Aa, b = 12.601(11) Aa, c = 11.552 Aa; 2 is in C2/m, a = 13.648(1) Aa, b = 16.852(1) Aa, c = 9.832(1) Aa, β = 125.980(1) {sup circle}. In 1 the U(VI) cations are present as (UO{sub 2}){sup 2+} uranyl ions that are coordinated by five oxygen atoms to give pentagonal bipyramids. These share two edges with two tungstate octahedra and single vertices with four additional octahedra, resulting in a sheet with the iriginite-type anion topology. Only water molecules are located in the interlayer. The structural units of 2 consist of (UO{sub 2}){sup 2+} uranyl oxy-fluoride pentagonal bipyramids present as either [UO{sub 2}F{sub 2}O{sub 3}]{sup -6} or [UO{sub 2}FO{sub 4}]{sup -5}, and strongly distorted tungstate octahedra. The linkage of uranyl pentagonal bipyramids and tungstate octahedra gives a unique sheet anion topology consisting of pentagons, squares and triangles. In 2, the uranyl tungstates sheets are connected into a novel electro-neutral three-dimensional framework through dimers of uranyl pentagonal bipyramids. These dimers connecting the sheets share an edge defined by F anions. 2 is the first example of a uranyl tungstate oxy-fluoride, and 1 and 2 are rare examples of uranyl compounds containing electro-neutral structural units.

  11. Studies on ZnO Nanorods Synthesized by Hydrothermal Method and their Characterization

    Directory of Open Access Journals (Sweden)

    B.H. Soni

    2014-01-01

    Full Text Available ZnO nanorods, with a wide band gap of 3.37 eV have been attracting much attention due to its wide range of applications. Looking to this aspect in the present paper, ZnO nanorods were synthesized by hydrothermal method at 120 C for 2 hrs in an autoclave by using zinc acetate and sodium hydroxide as the starting materials. The final product obtained was then characterized by Energy Dispersive analysis of X-rays (EDAX, X-ray powder diffraction (XRD, transmission electron microscopy (TEM, selected area electron diffraction (SAED and Raman Spectroscopy. X-ray diffraction and Raman spectra showed that ZnO nanorods are belonging to wurtzite structure without any impurity phases. The ZnO nanorods shows polycrystalline behaviour as observed from SAED pattern and the calculated lattice parameters from this pattern which matches with the XRD results.The optical properties of the ZnO nanorods were then further studied with the help of absorption, photoluminescence (PL and FTIR spectra. The optical energy band gap determined from the absorption spectra comes about 3.33 eV. In the photoluminescence spectra of ZnO nanorods the UV emission appears at 380 nm and strong blue emission appears at 445 nm. FTIR spectra indicate the existence of distinct characteristic absorption peak at 520 cm – 1 for ZnO stretching modes. The potential toxicity of nanosized ZnO nanorods were investigated using Staphylococcus aureus, Escherichia coli, Bacillus subtilis, Pseudomonas aeruginosa, Serratia marceseus and Proteus vulgaris bacteria as test organism.

  12. Morphological, structural and field emission characterization of hydrothermally synthesized MoS2-RGO nanocomposite

    Science.gov (United States)

    Bansode, Sanjeewani R.; Harpale, Kashmira; Khare, Ruchita T.; Walke, Pravin S.; More, Mahendra A.

    2016-11-01

    A few layered MoS2-RGO nanocomposite has been synthesized employing a facile hydrothermal synthesis route. The morphological and structural analysis performed using SEM, TEM, HRTEM and Raman spectroscopy clearly reveal formation of vertically aligned a few layer thick MoS2 sheets on RGO surface. Attempts have been made to reveal the influence of graphite oxide (GO) percentage on morphology of the nanocomposite. Furthermore, field emission (FE) investigations of as-synthesied MoS2-RGO nanocomposite are observed to be superior to the pristine MoS2 emitter. The values of turn-on field, defined at emission current density of 10 μA cm-2, are found to be 2.6 and 4.7 V μm-1 for the MoS2-RGO (5%) nanocomposite and pristine MoS2 emitters, respectively. The value of threshold field, defined at emission current density of 100 μA cm-2, is found to be 3.1 V μm-1 for MoS2-RGO nanocomposite. The emission current stability at the pre-set value of 1 μA over 3 h duration is found to be fairly good, characterized by current fluctuation within ±18% of the average value. The enhanced FE behavior for MoS2-RGO nanocomposite is attributed to a high enhancement factor (β) of 4128 and modulation of the electronic properties. The facile approach adopted herein can be extended to enhance various functionalities of other nanocomposites.

  13. Synthesis of Graphene-CdSe Composite by a Simple Hydrothermal Method and Its Photocatalytic Degradation of Organic Dyes

    Institute of Scientific and Technical Information of China (English)

    OH Won-Chun; CHEN Mingliang; CHO Kwangyoun; KIM Cheolkyu; MENG Zeda; ZHULei

    2011-01-01

    A graphene-CdSe composite was synthesized by a facile hydrothermal method,and characterized by X-ray diffiraction,scanning electron microscopy with energy dispersive X-ray analysis,transmission electron microscopy and UV-vis diffuse reflectance spectrophotometry.The graphene-CdSe composite efficiently catalyzed the photodegradation of methylene blue (MB),methyl orange (MO) and rhodamine B (Rh.B) in aqueous solution under UV or visible light irradiation.The graphene-CdSe composite exhibited a higher photocatalytic activity for the MB solution.

  14. Investigations on Bi{sub 25}FeO{sub 40} powders synthesized by hydrothermal and combustion-like processes

    Energy Technology Data Exchange (ETDEWEB)

    Köferstein, Roberto, E-mail: roberto.koeferstein@chemie.uni-halle.de; Buttlar, Toni; Ebbinghaus, Stefan G.

    2014-09-15

    The syntheses of phase-pure and stoichiometric iron sillenite (Bi{sub 25}FeO{sub 40}) powders by a hydrothermal (at ambient pressure) and a combustion-like process are described. Phase-pure samples were obtained in the hydrothermal reaction at 100 °C (1), whereas the combustion-like process leads to pure Bi{sub 25}FeO{sub 40} after calcination at 750 °C for 2 h (2a). The activation energy of the crystallite growth process of hydrothermally synthesized Bi{sub 25}FeO{sub 40} was calculated as 48(9) kJ mol{sup −1}. The peritectic point was determined as 797(1) °C. The optical band gaps of the samples are between 2.70(7) eV and 2.81(6) eV. Temperature and field-depending magnetization measurements (5−300 K) show a paramagnetic behaviour with a Curie constant of 55.66×10{sup −6} m{sup 3} K mol{sup −1} for sample 1 and C=57.82×10{sup −6} m{sup 3} K mol{sup −1} for sample 2a resulting in magnetic moments of µ{sub mag}=5.95(8) µ{sub B} mol{sup −1} and µ{sub mag}=6.07(4) µ{sub B} mol{sup −1}. The influence of amorphous iron-oxide as a result of non-stoichiometric Bi/Fe ratios in hydrothermal syntheses on the magnetic behaviour was additionally investigated. - Graphical abstract: Bi{sub 25}FeO{sub 40} powders were prepared by a hydrothermal method and a combustion process. The optical band gaps and the peritectic point were determined. The magnetic behaviour was investigated depending on the synthesis and the initial Bi/Fe ratios. The influence of amorphous iron-oxide on the magnetic properties was examined. - Highlights: • Two simple syntheses routes for stoichiometric Bi{sub 25}FeO{sub 40} powders using starch as polymerization agent. • Monitoring the phase evolution and crystallite growth kinetics during the syntheses. • Determination of the optical band gap and melting point. • Investigations of the magnetic behaviour of Bi{sub 25}FeO{sub 40} powders. • Influence of amorphous iron oxide and a non-stoichiometric Bi/Fe ratio on the

  15. Preparation of AgSnO2 composite powders by hydrothermal process

    Institute of Scientific and Technical Information of China (English)

    YANG Tian-zu; DU Zuo-juan; GU Ying-ying; QIU Xiao-yong; JIANG ming-xi

    2007-01-01

    Silver-tin oxide powders were synthesized by the hydrothermal method with Ag(NH3)2+ solution and Na2SnO3 solution as raw materials and Na2SO3 as reductant. The precipitation conditions of Na2SnO3 solution and the reduction conditions of Ag(NH3)2+ were also investigated. The powders prepared were characterized by differential thermal analysis (DTA), X-ray diffraction analysis (XRD), scanning electron microscope (SEM) and energy spectrum analysis. The results show that pH value of the solution is a key parameter in the formation of Sn(OH)4 precipitate and the reduction reaction of Ag(NH3)2+ can release H+ ions, which results in synchronous precipitation of Sn(OH)62- as Sn(OH)4. The reduction of Ag(NH3)2+ and precipitation of Na2SnO3 occur simultaneously and the coprecipitation of silver and tin oxide is reached by the hydrothermal method. The silver-tin oxide composite powders have mainly flake shape of about 0.3 μm in thickness and there exists homogeneous distribution of tin oxide and silver in the powder synthesized.

  16. Encapsulation of metal clusters within MFI via interzeolite transformations and direct hydrothermal syntheses and catalytic consequences of their confinement.

    Science.gov (United States)

    Goel, Sarika; Zones, Stacey I; Iglesia, Enrique

    2014-10-29

    The encapsulation of metal clusters (Pt, Ru, Rh) within MFI was achieved by exchanging cationic metal precursors into a parent zeolite (BEA, FAU), reducing them with H2 to form metal clusters, and transforming these zeolites into daughter structures of higher framework density (MFI) under hydrothermal conditions. These transformations required MFI seeds or organic templates for FAU parent zeolites, but not for BEA, and occurred with the retention of encapsulated clusters. Clusters uniform in size (1.3-1.7 nm) and exposing clean and accessible surfaces formed in BEA and FAU zeolites; their size remained essentially unchanged upon transformation into MFI. Encapsulation selectivities, determined from the relative hydrogenation rates of small (toluene) and large (alkyl arenes) molecules and defined as the ratio of the surface areas of all the clusters in the sample to that of external clusters, were very high (8.1-40.9) for both parent and daughter zeolites. Encapsulation into MFI via direct hydrothermal syntheses was unsuccessful because metal precursors precipitated prematurely at the pH and temperatures required for MFI synthesis. Delayed introduction of metal precursors and F(-) (instead of OH(-)) as the mineralizing agent in hydrothermal syntheses increased encapsulation selectivities, but they remained lower than those achieved via interzeolite transformations. These interconversions provide a general and robust strategy for encapsulation of metals when precursors can be introduced via exchange into a zeolite that can be transformed into target daughter zeolites with higher framework densities, whether spontaneously or by using seeds or structure-directing agents (SDA).

  17. Hydrothermal synthesis and photoelectrochemical performance enhancement of TiO{sub 2}/graphene composite in photo-generated cathodic protection

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Weiwei, E-mail: vivizhg@yahoo.com [College of Material Science and Engineering, Shandong University of Science and Technology, Qingdao 266590 (China); State Key Laboratory of Mining Disaster Prevention and Control Co-founded by Shandong Province and the Ministry of Science and Technology, Shandong University of Science and Technology, Qingdao 266590 (China); Guo, Hanlin; Sun, Haiqing [College of Material Science and Engineering, Shandong University of Science and Technology, Qingdao 266590 (China); Zeng, Rong-Chang [College of Material Science and Engineering, Shandong University of Science and Technology, Qingdao 266590 (China); State Key Laboratory of Mining Disaster Prevention and Control Co-founded by Shandong Province and the Ministry of Science and Technology, Shandong University of Science and Technology, Qingdao 266590 (China)

    2016-09-30

    Highlights: • TiO{sub 2}/graphene composites were synthesized through one-step hydrothermal method. • A bicrystalline framework of anatase and brookite formed. • Electrons transfer in the biphasic TiO{sub 2} results in electron-hole separation. • Graphene lead to a negative shift of the Fermi level. • The transfer barrier in the TiO{sub 2} and 304 stainless steel interface is decreased. - Abstract: TiO{sub 2}/graphene composites were synthesized through one-step hydrothermal method. The composites show an enhancement in photo-generated cathodic protection as the time-dependent profiles of photocurrent responses has confirmed. XRD data show that a bicrystalline framework of anatase and brookite formed as graphene provided donor groups in the hydrothermal process. The transfer of photoinduced electrons in the biphasic TiO{sub 2} results in effective electron-hole separation. Moreover, graphene lead to a negative shift of the Fermi level as evidenced by Mott–Schottky analysis, which decreases the Schottky barrier formed in the TiO{sub 2} and 304 stainless steel interface and results in the enhancement of photo-generated cathodic protection.

  18. Effects of pH and temperature on photocatalytic activity of PbTiO3 synthesized by hydrothermal method

    Science.gov (United States)

    Li, Yongyu; Sun, Haijie; Wang, Ning; Fang, Wenxue; Li, Zhongjun

    2014-11-01

    PbTiO3 photocatalyst was synthesized successfully by facile hydrothermal method. The effects of the hydrothermal reaction temperatures and the pH values of the systems on the photocatalytic activities of PbTiO3 were investigated in detail. The photocatalytic activities of samples were evaluated by the degradation of methyl orange (MO) aqueous solution under simulated solar irradiation. The as-obtained PbTiO3 sample exhibits anisotropical growth along the (0 0 1) plane, and its photocatalytic activity is about 3 times higher than that of PbTiO3 prepared by precipitation method. Moreover, the as-prepared PbTiO3 has high stability during photocatalytic oxidation process, and does not cause secondary pollution.

  19. Crystalline hydroxyapatite coatings synthesized under hydrothermal conditions on modified titanium substrates

    Energy Technology Data Exchange (ETDEWEB)

    Suchanek, Katarzyna, E-mail: Katarzyna.Suchanek@ifj.edu.pl [The Henryk Niewodniczański Institute of Nuclear Physics, Polish Academy of Sciences, Radzikowskiego Street 152, 31-342 Krakow (Poland); Bartkowiak, Amanda [The Henryk Niewodniczański Institute of Nuclear Physics, Polish Academy of Sciences, Radzikowskiego Street 152, 31-342 Krakow (Poland); Gdowik, Agnieszka [Faculty of Physics and Applied Computer Science, AGH University of Science and Technology, Mickiewicza 30, 30-059 Krakow (Poland); Perzanowski, Marcin [The Henryk Niewodniczański Institute of Nuclear Physics, Polish Academy of Sciences, Radzikowskiego Street 152, 31-342 Krakow (Poland); Kąc, Sławomir [Faculty of Metals Engineering and Industrial Computer Science, AGH University of Science and Technology, Mickiewica 30, 30-059 Krakow (Poland); Szaraniec, Barbara [Department of Biomaterials, AGH University of Science and Technology, Mickiewicza 30, 30-059 Krakow (Poland); Suchanek, Mateusz [Department of Chemistry and Physics, University of Agriculture in Krakow, Mickiewicza 21, 31-120 Krakow (Poland); Marszałek, Marta [The Henryk Niewodniczański Institute of Nuclear Physics, Polish Academy of Sciences, Radzikowskiego Street 152, 31-342 Krakow (Poland)

    2015-06-01

    Hydroxyapatite coatings were successfully produced on modified titanium substrates via hydrothermal synthesis in a Ca(EDTA){sup 2−} and (NH{sub 4}){sub 2}HPO{sub 4} solution. The morphology of modified titanium substrates as well as hydroxyapatite coatings was studied using scanning electron microcopy and phase identification by X-ray diffraction, and Raman and FTIR spectroscopy. The results show that the nucleation and growth of hydroxyapatite needle-like crystals with hexagonal symmetry occurred only on titanium substrates both chemically and thermally treated. No hydroxyapatite phase was detected on only acid etched Ti metal. This finding demonstrates that only a particular titanium surface treatment can effectively induce the apatite nucleation under hydrothermal conditions. - Highlights: • Bioactivation of titanium substrate by chemical and heat treatments • Precipitation of hydroxyapatite on modified titanium plates • Hydrothermal crystallization of hydroxyapatite by chelate decomposition method.

  20. Photocatalysis of WO3 Nanoplates Synthesized by Conventional-Hydrothermal and Microwave-Hydrothermal Methods and of Commercial WO3 Nanorods

    Directory of Open Access Journals (Sweden)

    Jarupat Sungpanich

    2014-01-01

    Full Text Available The degradation of methylene blue (MB dye by tungsten oxide (WO3 photocatalyst synthesized by the 200°C conventional-hydrothermal (C-H and 270 W microwave-hydrothermal (M-H methods and commercial WO3 was studied under UV light irradiation for 360 min. The photocatalysts were characterized by X-ray diffraction (XRD, scanning electron microscopy (SEM, transmission electron microscopy (TEM, Fourier transform infrared (FTIR spectroscopy, Raman spectrophotometry, and UV visible spectroscopy to determine phase, morphology, vibration mode, and optical property. The BET analysis revealed the specific surface area of 29.74, 37.25, and 33.56 m2/g for the C-H WO3 nanoplates, M-H WO3 nanoplates, and commercial WO3 nanorods, respectively. In this research, the M-H WO3 nanoplates have the highest photocatalytic efficiency of 90.07% within 360 min, comparing to the C-H WO3 nanoplates and even commercial WO3 nanorods.

  1. Degradation of Rhodamine B Dye by TiO2 Nanotubes Photocatalyst Synthesized via Alkaline Hydrothermal Method

    Directory of Open Access Journals (Sweden)

    T Mazlina Mat Darus

    2015-01-01

    Full Text Available Titanium dioxide (TiO2 nanotubes have successfully been synthesized by using one step approach of hydrothermal method. Commercial TiO2 (anatase powder was used as precursor to synthesize the TiO2 nanotubes. The TiO2 nanotubes were synthesized at 120 °C/20 hrs in an alkaline solution of NaOH. The photocatalytic study of the as-synthesized samples was conducted by analyzing the degradation of Rhodamine B (Rh B dye under UV light irradiation. Rh B is a toxic dye which is commonly used in textile industry. It is the one of the most common pollutants in the effluents and highly soluble in water. A comparison study was carried out in order to investigate the photocatalytic activity between the synthesized TiO2 nanotubes and the commercial TiO2 nanoparticles. Results show that the TiO2 nanotubes exhibits better photocatalytic activity in the degradation of Rh B as compared to the TiO2 nanoparticles.

  2. Enhanced Photo catalytic Activity of ZnO/CuO Nano comp osites Synthesized by Hydrothermal Metho d

    Institute of Scientific and Technical Information of China (English)

    Tongqin Chang; Zijiong Li∗; Gaoqian Yun; Yong Jia; Hongjun Yang

    2013-01-01

    In this paper, we have demonstrated a facile and low-cost synthesis of the ZnO/CuO nanocom-posites by two-step hydrothermal methods. The photocatalytic properties of the as-synthesized ZnO/CuO nanocomposites have been evaluated by the photodegradation of methylene blue (MB) and methyleneorange (MO) under UV irradiation. Experimental results show that MB and MO can be degraded completely within 15 and 25 min by the ZnO/CuO nanocomposites and its photodegradation rate is 6 times faster than that of pure ZnO. This enhanced photocatalytic activity can be ascribed to the low recombination probability of photo-induced carriers due to the efficient charge transfer in the nanocomposites. The as-synthesized ZnO/CuO nanocomposite may be a promising candidate for dye photodegradation of wastewaters.

  3. Comparison of intact polar lipid with microbial community composition of vent deposits of the Rainbow and Lucky Strike hydrothermal fields

    NARCIS (Netherlands)

    Gibson, R.A.; van der Meer, M.T.J.; Hopmans, E.C.; Reysenbach, A.-L.; Schouten, S.; Sinninghe Damsté, J.S.

    2013-01-01

    The intact polar lipid (IPL) composition of twelve hydrothermal vent deposits from the Rainbow (RHF) and Lucky Strike hydrothermal fields (LSHF) has been investigated in order to assess its utility as a proxy for microbial community composition associated with deep-sea hydrothermal locations. Gene-b

  4. Comparison of intact polar lipid with microbial community composition of vent deposits of the Rainbow and Lucky Strike hydrothermal fields

    NARCIS (Netherlands)

    Gibson, R.A.; van der Meer, M.T.J.; Hopmans, E.C.; Reysenbach, A.-L.; Schouten, S.; Sinninghe Damsté, J.S.

    2013-01-01

    The intact polar lipid (IPL) composition of twelve hydrothermal vent deposits from the Rainbow (RHF) and Lucky Strike hydrothermal fields (LSHF) has been investigated in order to assess its utility as a proxy for microbial community composition associated with deep-sea hydrothermal locations.

  5. Electronic structure and magnetic properties of FeWO{sub 4} nanocrystals synthesized by the microwave-hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Almeida, M.A.P. [INCTMN-DQ-Universidade Federal de Sao Carlos, Sao Carlos, P.O. Box 676, 13565-905, SP (Brazil); Cavalcante, L.S., E-mail: laeciosc@bol.com.br [INCTMN-Universidade Estadual, Paulista, P.O. Box 355, 14801-907, Araraquara, SP (Brazil); Morilla-Santos, C.; Filho, P.N. Lisboa [MAv-Universidade Estadual, Paulista, P.O. Box 473, 17033-360, Bauru, SP (Brazil); Beltran, A.; Andres, J.; Gracia, L. [Department de Quimica Fisica i Analitica, Universitat Jaume I, E-12071 Castello (Spain); Longo, E. [INCTMN-DQ-Universidade Federal de Sao Carlos, Sao Carlos, P.O. Box 676, 13565-905, SP (Brazil); INCTMN-Universidade Estadual, Paulista, P.O. Box 355, 14801-907, Araraquara, SP (Brazil)

    2012-11-15

    This communication reports that FeWO{sub 4} nanocrystals were successfully synthesized by the microwave-hydrothermal method at 443 K for 1 h. The structure and shape of these nanocrystals were characterized by X-ray diffraction, Rietveld refinement, and transmission electron microscopy. The experimental results and first principles calculations were combined to explain the electronic structure and magnetic properties. Experimental data were obtained by magnetization measurements for different applied magnetic fields. Theoretical calculations revealed that magnetic properties of FeWO{sub 4} nanocrystals can be assigned to two magnetic orderings with parallel or antiparallel spins in adjacent chains. These factors are crucial to understanding of competition between ferro- and antiferromagnetic behavior. Highlights: Black-Right-Pointing-Pointer Monophasic FeWO{sub 4} nanocrystals were synthesized by the microwave-hydrothermal method. Black-Right-Pointing-Pointer Rietveld refinement and clusters model for monoclinic structure Black-Right-Pointing-Pointer Magnetic properties of FeWO{sub 4} nanocrystals at different temperatures.

  6. Influence of Li doping on the optical and magnetic properties of ZnO nanorods synthesized by low temperature hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Kung, C.Y., E-mail: cykung@dragon.nchu.edu.tw [Department of Electrical Engineering, National Chung Hsing University, Taichung 40227, Taiwan (China); Lin, C.C. [Department of Electrical Engineering, National Chung Hsing University, Taichung 40227, Taiwan (China); Young, S.L., E-mail: slyoung@mail.hust.edu.tw [Department of Electronic Engineering, Hsiuping University of Science and Technology, Taichung 41280, Taiwan (China); Horng, Lance; Shih, Y.T. [Department of Physics, National Changhua University of Education, Changhua 50007, Taiwan (China); Kao, M.C.; Chen, H.Z. [Department of Electronic Engineering, Hsiuping University of Science and Technology, Taichung 41280, Taiwan (China); Lin, H.H. [Department and Graduate School of Electrical Engineering, Hsiuping University of Science and Technology, Taichung 41280, Taiwan (China); Lin, J.H.; Wang, S.J.; Li, J.M. [Department of Electronic Engineering, Hsiuping University of Science and Technology, Taichung 41280, Taiwan (China)

    2013-02-01

    Well-defined pure Zn{sub 1−x}Li{sub x}O (x = 0, 0.05 and 0.1) nanorods were hydrothermally synthesized at the low temperature of 90 °C. The X-ray diffraction patterns of all three compositions with a single diffraction peak (0002) showed the same wurtzite hexagonal structure due to the similar radius of Zn and Li. The optical and magnetic properties were influenced by the oxygen vacancies induced by Li doping in the ZnO nanorods. The Raman shift spectrum indicated a slight increasement of oxygen vacancies which enhanced the green emission and ferromagnetism by the doping of Li in the ZnO nanorods. Besides, p-type ZnO:Li semiconductor nanorods were obtained by Li doping. The characteristics of the UV photodetector with p-ZnO:Li nanorod/n-Si structure were also measured. - Highlights: ► Zn{sub 1−x}Li{sub x}O nanorods have grown by hydrothermal method at a low temperature of 90 °C. ► Doping of Li increases the doping-induced defects. ► Saturation magnetization increases as Li content increases. ► ZnO-based UV photodetector with nanorod structure is achieved.

  7. [Light Absorption Characteristics of FeS2-Fe1-xS Heterostructures Synthesized under Hydrothermal Conditions].

    Science.gov (United States)

    Liu, Jia; Huang, Fei; Meng, Lin; Yu, Hao-ran; Chen, Ying-hua

    2015-05-01

    Fe-S series, especially FeS2 and Fe1-x S is the main component of crustal rocks as important metal sulphides. Pyrite (FeS2) shows a promising vision in solar cell materials for its high absorption coefficient and suitable band gap. Predecessors have done some researches on the photovoltaic properties of Fe-S series under different conditions. However, little researches have been done on the coexisted sulphide of FeS2 and Fe1-xS. FeS2 and Fe1-xS often appear as symbiotically due to their similar formation conditions. So the study on the optical absorption characteristics of FeS2 and Fe1-xS are of important significance. In order to study the optical absorption characteristics of FeS2-Fe1-xS heterostructures, using the SEM and XRD to characterize the morphology, composition and structure, respectively. The results show that the samples were cubic pyrite with a certain amount of pyrhotite (Fe1-xS). The crystal partical size was between 5 and 10 nm. Measurement of the absorption spectrum was performed using Cary 500 UV-Vis-NIR spectrophotoineter, acquiring the results of 1 860-1 889 nm, and the absorption peak in 1879nm. According to the band gap (eV) formula, the band gap value is calculated to be 0. 657 8 eV. The extreme electrical-to-optical conversion efficiency achieved was about 15%. By the first principles, we analysed the reason of the changing of the band gap value, and then compared the result with previous one. The internal structure of mineral is the important factor affecting the photoelectric conversion. The light absorption characteristics of FeS2-Fel-xS heterostructures synthesized under hydrothermal conditions is better than the characteristics from natural pyrite with defects of Co and Ni. The heterostructures can improve the electrical-to-optical conversion efficiency and provide scientific basis for the absorption characteristics research of Fe-S series materials.

  8. Microwave assisted hydrothermal synthesis and characterization of ZnO–TNT composites

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Sung Hun; Gyawali, Gobinda; Adhikari, Rajesh [Department of Metallurgy and Materials Engineering, SunMoon University, Asan (Korea, Republic of); Kim, Tae Ho [Department of Environmental Engineering, SunMoon University, Asan (Korea, Republic of); Lee, Soo Wohn, E-mail: swlee@sunmoon.ac.kr [Department of Environmental Engineering, SunMoon University, Asan (Korea, Republic of)

    2014-06-01

    TiO{sub 2} nanotubes with different contents of ZnO (3–40 wt.% ZnO) have been successfully synthesized by microwave assisted hydrothermal process by using commercial TiO{sub 2}-P25 as a precursor. The phase and crystallinity of the obtained ZnO–TNT were analyzed by X-ray Diffraction (XRD). The surface area of the ZnO–TNT was determined by BET method. The effect of the different contents of ZnO on morphology of TiO{sub 2} nanotubes was investigated by SEM and TEM. Optical properties and band gap energy of ZnO–TNT were calculated by using UV–vis DRS spectroscopy and modified Kubelka–Munk equation. Photocatalytic performance of ZnO–TNT was investigated by degradation of rhodamine B (RhB) dye under UV and visible light irradiation. Increasing ZnO content in TNT gradually decreased the diameter and length of nanotubes. Furthermore, addition of 40 wt.% ZnO into the TNT exceeded the saturation limit of ion exchangeability of Zn{sup 2+} and Na{sup +} ions and aggregation of finely dispersed ZnO particles on the surface of TNT were observed. The ZnO–TNT has shown relatively larger band gap energies than that of TiO{sub 2}-P25. However, ZnO–TNT has shown considerable increase in photo-activity for degradation of RhB dye in visible light as compared to UV light irradiation. - Highlights: • ZnO–TNT composites were successfully synthesized. • Investigation of the structural changes in the composites is confirmed. • The photocatalytic activity of the composites was studied. • Composites exhibited better performance under visible light than in UV light.

  9. Improvement to the Corrosion Resistance of Ti-Based Implants Using Hydrothermally Synthesized Nanostructured Anatase Coatings

    Directory of Open Access Journals (Sweden)

    Martina Lorenzetti

    2014-01-01

    Full Text Available The electrochemical behavior of polycrystalline TiO2 anatase coatings prepared by a one-step hydrothermal synthesis on commercially pure (CP Ti grade 2 and a Ti13Nb13Zr alloy for bone implants was investigated in Hank’s solution at 37.5 °C. The aim was to verify to what extent the in-situ-grown anatase improved the behavior of the substrate in comparison to the bare substrates. Tafel-plot extrapolations from the potentiodynamic curves revealed a substantial improvement in the corrosion potentials for the anatase coatings. Moreover, the coatings grown on titanium also exhibited lower corrosion-current densities, indicating a longer survival of the implant. The results were explained by considering the effects of crystal morphology, coating thickness and porosity. Evidence for the existing porosity was obtained from corrosion and nano-indentation tests. The overall results indicated that the hydrothermally prepared anatase coatings, with the appropriate morphology and surface properties, have attractive prospects for use in medical devices, since better corrosion protection of the implant can be expected.

  10. Effect of Surfactants on the Structure and Morphology of Magnesium Borate Hydroxide Nanowhiskers Synthesized by Hydrothermal Route

    Directory of Open Access Journals (Sweden)

    Kulkarni Shrinivas

    2009-01-01

    Full Text Available Abstract Magnesium borate hydroxide (MBH nanowhiskers were synthesized using a one step hydrothermal process with different surfactants. The effect surfactants have on the structure and morphology of the MBH nanowhiskers has been investigated. The X-ray diffraction profile confirms that the as-synthesized material is of single phase, monoclinic MgBO2(OH. The variations in the size and shape of the different MBH nanowhiskers have been discussed based on the surface morphology analysis. The annealing of MBH nanowhiskers at 500 °C for 4 h has significant effect on the crystal structure and surface morphology. The UV–vis absorption spectra of the MBH nanowhiskers synthesized with and without surfactants show enhanced absorption in the low-wavelength region, and their optical band gaps were estimated from the optical band edge plots. The photoluminescence spectra of the MBH nanowhiskers produced with and without surfactants show broad emission band with the peak maximum at around 400 nm, which confirms the dominant contribution from the surface defect states.

  11. Synthesize TiO2 microspheres self-assembled from nanorods via hydrothermal treatment

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The TiO2 microspheres were deposited on the glass substrates under certain conditions via hydro-thermal reaction using 0.15 mol·L?1 TiCl3 saturated NaCl aqueous solution adding urea as an additive. The TiO2 is characterized rutile by results of SEM,TEM and XRD techniques,the TiO2 microspheres are large scale assembled from TiO2 nanorods. The affections on the products by the factors of the con-tents of urea being an additive(the key techniques) ,the reaction temperature,the reaction time and the concentration of TiCl3 were studied. The optimum condition was found,and the mechanism of reac-tions was discussed also.

  12. Synthesis and Electronic Transport of Hydrothermally Synthesized p-Type Na-Doped SnSe

    Science.gov (United States)

    Yang, Zong-Ren; Chen, Wei-Hao; Liu, Chia-Jyi

    2016-11-01

    A series of polycrystalline Sn1-x Na x Se with x = 0.00, 0.02, 0.04 and 0.10 were fabricated using hydrothermal synthesis followed by evacuated-and-encapsulated sintering. The as-fabricated materials were characterized using powder x-ray diffraction and electronic transport. The resulting materials were single phase. Partial replacement of Na for Sn leads to a simultaneous increase of electrical conductivity and thermopower. The x = 0.04 sample has the largest power factor among the series of the samples. Upon partial replacement of Na for Sn, the power factor is significantly enhanced as compared to the undoped SnSe. The maximum ZT value of ˜0.4 was achieved for Sn0.96Na0.04Se at 550 K.

  13. Structure and electrochemistry of scaling nano C-LiFePO4 synthesized by hydrothermal route: Complexing agent effect

    Science.gov (United States)

    Brochu, F.; Guerfi, A.; Trottier, J.; Kopeć, M.; Mauger, A.; Groult, H.; Julien, C. M.; Zaghib, K.

    2012-09-01

    Submicronic particles of LiFePO4 were synthesized by hydrothermal method at 185 °C assisted by carboxylic acid route. In this work, we used citric acid to control the pH of the final products and studied the influence of synthetic conditions on the physical and electrochemical properties of LiFePO4. Structural characterization includes XRD, SEM, TEM and FTIR experiments. The powder quality was investigated by magnetic measurements. Electrochemical features of C-LiFePO4 in Li cell using 1 mol L-1 LiPF6-EC-DEC electrolyte show an excellent capacity retention of 158 mAh g-1 for material prepared with R(citric acid/Fe) = 7 mol%.

  14. Enhanced Visible-Light Photocatalytic Activity of C/Ce-Codoped ZnO Nanoellipsoids Synthesized by Hydrothermal Method

    Science.gov (United States)

    Ha, Luu Thi Viet; Dai, Luu Minh; Nhiem, Dao Ngoc; Van Cuong, Nguyen

    2016-08-01

    C/Ce-codoped ZnO nanomaterial has been synthesized by a hydrothermal method and its physical properties and characterization investigated using thermogravimetric and differential thermal analysis (TG-DTA), x-ray diffraction (XRD) analysis, Fourier-transform infrared (FTIR) spectroscopy, energy-dispersive x-ray (EDX) spectroscopy, UV-Vis diffuse reflectance spectroscopy, and scanning electron microscopy (SEM). The photocatalytic activity of the nanomaterial was examined using methylene blue as organic dye under visible-light source. The results show that the C/Ce-codoped ZnO nanomaterial exhibited higher photocatalytic activity under visible-light irradiation compared with undoped ZnO, Ce-doped ZnO or C-doped ZnO nanomaterials. Such enhancement of the photocatalytic activity of C/Ce-codoped ZnO under visible-light irradiation suggests that these nanoparticles might have good applications in optoelectronics and wastewater treatment.

  15. Development of a hydrothermal method to synthesize spherical ZnSe nanoparticles: Appropriate templates for hollow nanostructures

    Directory of Open Access Journals (Sweden)

    S. Gharibe

    2014-01-01

    Full Text Available Hydrothermal method was used to synthesize pure ZnSe nanosphere materials. The effects of the reducing agent amount, the reaction time and temperature were investigated on the purity of ZnSe. Also, the effects of surfactants such as sodium dodecyl sulfate (SDS (anionic and cetyl trimethylammonium bromide (CTAB (cationic were studied on the morphology of ZnSe. The prepared nanospheres were characterized using XRD, SEM, TEM and UV-Vis spectroscopy. Through these techniques, it was found that the pure ZnSe nanoparticles have a zinc blend structure and in a spherical form with average diameter of 30 nm. DOI: http://dx.doi.org/10.4314/bcse.v28i1.5

  16. Structural analysis of ZnO nanowires synthesized by using a low-temperature hydro-thermal method

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Sang Hyo; Lee, Jun Seok; Ko, Won Bae; Kang, Tae Seong; Hong, Jin Pyo [Hanyang University, Seoul (Korea, Republic of); Cha, Seung Nam [Samsung Institute of Advanced Technology, Yongin (Korea, Republic of)

    2012-05-15

    The structural properties of vertically aligned ZnO nanowires (NWs) prepared using hydrothermal synthesis at various temperatures and different precursor concentrations are systematically described. The ZnO NWs were synthesized on ZnO seed layers via an aqueous solution method with zinc nitrate (Zn(NO{sub 3}){sub 2}·6H{sub 2}O) hexahydrate and hexamethylenetetramine (HMT). The growth speed and the shape of the ZnO NWs were determined for various mole concentrations. A structural analysis of the ZnO NWs was performed using X-ray diffraction, scanning electron microscopy and tunneling electron microscopy. Finally, the correlation of structural results with growth conditions, such as the mole concentration and the growth temperature of chemical precursors, based on Gibbs free energy.

  17. Hydrothermal Habitats: Measurements of Bulk Microbial Elemental Composition, and Models of Hydrothermal Influences on the Evolution of Dwarf Planets

    Science.gov (United States)

    Neveu, Marc Francois Laurent

    Finding habitable worlds is a key driver of solar system exploration. Many solar system missions seek environments providing liquid water, energy, and nutrients, the three ingredients necessary to sustain life. Such environments include hydrothermal systems, spatially-confined systems where hot aqueous fluid circulates through rock by convection. I sought to characterize hydrothermal microbial communities, collected in hot spring sediments and mats at Yellowstone National Park, USA, by measuring their bulk elemental composition. To do so, one must minimize the contribution of non-biological material to the samples analyzed. I demonstrate that this can be achieved using a separation method that takes advantage of the density contrast between cells and sediment and preserves cellular elemental contents. Using this method, I show that in spite of the tremendous physical, chemical, and taxonomic diversity of Yellowstone hot springs, the composition of microorganisms there is surprisingly ordinary. This suggests the existence of a stoichiometric envelope common to all life as we know it. Thus, future planetary investigations could use elemental fingerprints to assess the astrobiological potential of hydrothermal settings beyond Earth. Indeed, hydrothermal activity may be widespread in the solar system. Most solar system worlds larger than 200 km in radius are dwarf planets, likely composed of an icy, cometary mantle surrounding a rocky, chondritic core. I enhance a dwarf planet evolution code, including the effects of core fracturing and hydrothermal circulation, to demonstrate that dwarf planets likely have undergone extensive water-rock interaction. This supports observations of aqueous products on their surfaces. I simulate the alteration of chondritic rock by pure water or cometary fluid to show that aqueous alteration feeds back on geophysical evolution: it modifies the fluid antifreeze content, affecting its persistence over geological timescales; and the

  18. The effect of poly vinyl alcohol (PVA) surfactant on phase formation and magnetic properties of hydrothermally synthesized CoFe2O4 nanoparticles

    Science.gov (United States)

    Jalalian, M.; Mirkazemi, S. M.; Alamolhoda, S.

    2016-12-01

    Nanoparticles of CoFe2O4 were synthesized by hydrothermal process at 190 °C with and without poly vinyl alcohol (PVA) addition using treatment durations of 1.5-6 h. The synthesized powders were characterized with X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscope (SEM), Field emission scanning electron microscope (FESEM) and vibration sample magnetometer (VSM) techniques. XRD results show presence of CoFe2O4 as the main phase and Co3O4 as the lateral phase in some samples. The results show that in the samples synthesized without PVA addition considerable amount of lateral phase is present after 3 h of hydrothermal treatment while with PVA addition this phase is undetectable in the XRD patterns of the sample synthesized at the same conditions. Microstructural studies represent increasing of particle size with increasing of hydrothermal duration and formation of coarser particles with PVA addition. The highest maximum magnetization (Mmax) values in both of the samples that were synthesized with and without PVA addition are about 59 emu/g that were obtained after 4.5 h of hydrothermal treatment. Intrinsic coercive field (iHc) value of the sample without PVA addition increases from 210 to 430 Oe. While with PVA addition the iHc value changes from 83 Oe to 493 Oe. The mechanism of changes in Mmax and iHc values has been explained.

  19. Hydrothermal Synthesis and Structural Characterization of NiO/SnO2 Composites and Hydrogen Sensing Properties

    Directory of Open Access Journals (Sweden)

    Chao Wei

    2015-01-01

    Full Text Available Pure SnO2 and NiO doped SnO2 nanostructures were successfully synthesized via a simple and environment-friendly hydrothermal method. X-ray powder diffraction (XRD, scanning electron microscopy (SEM, energy dispersive X-ray spectroscopy (EDS, and X-ray photoelectron spectra (XPS were used to investigate the crystalline structures, surface morphologies and microstructures, and element components and their valences of the as-synthesized samples. Furthermore, planar chemical gas sensors based on the synthesized pure SnO2 and NiO/SnO2 composites were fabricated and their sensing performances to hydrogen, an important fault characteristic gas dissolved in power transformer oil, were investigated in detail. Gas sensing experiments indicate that the NiO/SnO2 composites showed much higher gas response and lower working temperature than those of pure SnO2, which could be ascribed to the formation of p-n heterojunctions between p-type NiO and n-type SnO2. These results demonstrate that the as-synthesized NiO/SnO2 composites a promising hydrogen sensing material.

  20. Rapid hydrothermal route to synthesize cubic-phase gadolinium oxide nanorods

    Indian Academy of Sciences (India)

    Samiran Hazarika; Nibedita Paul; Dambarudhar Mohanta

    2014-06-01

    An inexpensive fabrication route and growth mechanism is being reported for obtaining quality gadolinium oxide (Gd2O3) nanoscale rods. The elongated nanoscale systems, as produced via a hydrothermal process, were characterized by X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), optical absorption spectroscopy, photoluminescence (PL) spectroscopy, Raman spectroscopy and magnetic hysteresis measurements. XRD patterns of the nanorods, as-prepared from independent precursors of different pH, depict a cubic crystal phase and an average crystallite size of 5-6.5 nm. As revealed from HRTEM micrographs, diameter of the nanorods prepared at pH = 13.3 (∼ 7nm) was much smaller than the rods prepared at pH = 10.8 (∼ 19nm). However, the aspect ratio was more than double in the former case than the latter case. PL response was found to be dominated by defect mediated emissions, whereas Raman spectrum of a given specimen (pH = 10.8) has revealed characteristic g + g modes of cubic phase of Gd2O3 nanorods, apart from other independent modes. Furthermore, ∼ plot of the nanorod system (pH = 10.8) exhibited slight departure from the ideal superparamagnetic behaviour, with low remanence and coercive field values. The exploitation of one-dimensional Gd2O3 nanorods have immense potential in the production of advanced contrast agents, smart drives and also in making novel ferrofluids of technological relevance.

  1. Structural, morphological and gas sensing study of zinc doped tin oxide nanoparticles synthesized via hydrothermal technique

    Science.gov (United States)

    Singh, Davender; Kundu, Virender Singh; Maan, A. S.

    2016-07-01

    The pure and Zn-doped SnO2 nanoparticles were prepared successfully by hydrothermal route on large scale having different doping concentration of zinc from 0 to 0.20%. The calcined nanoparticles were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM) for structural and morphological studies. XRD analyses reveal that the nanoparticles of these doping concentrations are polycrystalline in nature and existed as tetragonal rutile structure, SEM study of images confirms the existence of very small, homogeneously distributed, and spherical nanoparticles. The particles size of the nanoparticles was calculated by Scherrer formula and was found in the range of 9-21 nm. The presence of dopant (i.e. zinc) and formation of Sn-O phase and hydrous nature of Zn-doped SnO2 nanoparticles are confirmed by EDX and FTIR study. The gas sensing properties of pure and Zn-doped SnO2 nanoparticles were investigated for various concentrations of methanol, ethanol and acetone at different operating temperatures and it has been found that with doping concentration of zinc (x = 0.20%) shows the maximum response 78% to methanol, 65% to ethanol and 62% to acetone respectively at different operating temperature within the measurement limit for a concentration of 100 ppm of each gases.

  2. Multilayered composite microgels synthesized by surfactant-free seeded polymerization.

    Science.gov (United States)

    Suzuki, Daisuke; Yamagata, Tomoyo; Murai, Masaki

    2013-08-20

    We report on a simple and rapid method to produce multilayered composite microgels. Thermosensitive microgels were synthesized by aqueous free radical precipitation polymerization using N-isopropylacrylamide (NIPAm) as a monomer. Using the microgels as cores, surfactant-free seeded polymerization of an oil-soluble monomer, glycidyl methacrylate (GMA), was carried out at 70 °C, where the microgels were highly deswollen in water. All of the oil-soluble monomers were polymerized, and the resultant polymers were attached on the pre-existing microgel cores, resulting in hard shell formation. It is worth mentioning that secondary particles of oil-soluble monomers have never been formed during the polymerization. The composite microgels were characterized by electron microscopy and dynamic light scattering. In particular, X-ray photoelectron spectroscopy (XPS) measurements revealed that the surface of the composite microgels was composed of a hydrogel layer, although microgel cores were covered by polyGMA shell. The mechanism of the trilayered composite microgel formation will be discussed.

  3. Microwave radiation hydrothermal synthesis and characterization of micro- and mesoporous composite molecular sieve Y/SBA-15

    Directory of Open Access Journals (Sweden)

    Wenyuan Wu

    2017-05-01

    Full Text Available A microwave radiation hydrothermal method to control synthesis of micro- and mesoporous Y/SBA-15 composite molecular sieves was reported. The synthesized SBA-15 and Y/SBA-15 were characterized by scanning electron microscopy (SEM and N2 adsorption–desorption. The three kinds of different concentrations of hydrochloric acid (0.75 M, 2 M and 3.25 M were used to investigate the effect on Y/SBA-15. The analysis results of the composite products indicated that the optimization synthesis condition employed zeolite type Y and TEOS as silicon sources under 0.75 M hydrochloric acid by the microwave radiation hydrothermal synthesis method. The N2 adsorption–desorption test results of micro–mesoporous composite molecular sieve type Y/SBA-15 in mesoporous extent indicated that SBET is 355.529 m2/g, D‾BET is 4.050 nm, and mesoporous aperture focuses on the distribution region of 5.3 nm. It was found that the received composite product has an appropriate proportion of smaller size, larger size pore structure and the thicker pore wall. In addition, its internal channels have a high degree of order and smooth flow in long-range channels.

  4. The detection of genomic DNA from bacterial cells using iron oxide nanoparticles synthesized by a hydrothermal process

    Science.gov (United States)

    Kim, Young-Sung; Kim, Ki-Chul; Hong, Tae-Whan

    2010-04-01

    We used iron oxide nanoparticles in order to extract purified DNA from bacterial cells. Magnetite (Fe3O4) and maghemite (γ-Fe2O3) are synthesized with FeSO4·7H2O via a hydrothermal process and used as a medium to detect DNA. Various characterizations were performed including X-ray powder diffraction (XRD), high resolution transmission electron microscopy (HRTEM), field emission scanning electron microscopy, vibrating sample magnetometry, and Mössbauer spectroscopy. According to the XRD results, the XRD peaks of the synthesized magnetite and maghemite nanoparticles corresponded well with JCPDS standard data, respectively. The particle size of the iron oxide nanoparticles was about 20 nm, and the particle shape was almost spherical, which was confirmed by observation of the HRTEM image. The magnetite nanoparticles have a face-centeredcubic inverse spinel structure with a space group Fd bar 3 m, as confirmed by HRTEM and Mössbauer spectroscopy analyses. An agarose gel eletrophoresis analysis was performed to confirm the extraction ability of DNA using these iron oxide nanoparticles, revealing stronger reaction of the maghemite nanoparticles than the magnetite nanoparticles.

  5. VUV-Photocatalytic Degradation of Bezafibrate by Hydrothermally Synthesized Enhanced {001} Facets TiO2/Ti Film.

    Science.gov (United States)

    Sayed, Murtaza; Fu, Pingfeng; Shah, Luqman Ali; Khan, Hasan M; Nisar, Jan; Ismail, M; Zhang, Pengyi

    2016-01-14

    In the present study, a novel TiO2/Ti film with enhanced {001} facets was synthesized by the hydrothermal technique followed by calcination for studying the removal of bezafibrate (BZF), from an aqueous environment. The synthesized photocatalyst was characterized by FE-SEM, XRD, HR-TEM, and PL-technique. The second-order rate constant of (•)OH with BZF was found to be 5.66 × 10(9) M(-1) s(-1). The steady state [(•)OH] was measured as 1.16 × 10(-11) M, on the basis of oxidation of terephthalic acid. The photocatalytic degradation of BZF followed pseudo-first-order kinetics according to the Langmuir-Hinshelwood model (k1 = 2.617 mg L(-1) min(-1) and k2 = 0.0796 (mg L(-1))(-1)). The effects of concentration and the nature of various additives including inorganic anions (NO3(-), NO2(-), HCO3(-), CO3(2-), Cl(-)) and organic species (fulvic acid) and initial solution pHs (2, 4, 6, 9) on photocatalytic degradation of BZF were investigated. It was found that the nature and concentration of studied additives significantly affected the photocatalytic degradation of BZF. The efficiency of the photocatalytic degradation process in terms of electrical energy per order was estimated. Degradation schemes were proposed on the basis of the identified degradation byproducts by ultraperformance liquid chromatography.

  6. Au-controlled enhancement of photoluminescence of NiS nanostructures synthesized via a microwave-assisted hydrothermal technique

    Energy Technology Data Exchange (ETDEWEB)

    Linganiso, Ella Cebisa [DST/CSIR Nanotech Innovation Centre, National Centre for Nano-structured Materials, Council for Scientific and Industrial Research, PO Box 395, Pretoria 0001 (South Africa); Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand, Private Bag 3, Wits, 2050 Johannesburg (South Africa); Mwakikunga, Bonex Wakufwa, E-mail: bmwakikunga@csir.co.za [DST/CSIR Nanotech Innovation Centre, National Centre for Nano-structured Materials, Council for Scientific and Industrial Research, PO Box 395, Pretoria 0001 (South Africa); Department of Physics and Biochemical Sciences, The Polytechnic of the University of Malawi, Private Bag 303, Chichiri, Blantyre 0003 (Malawi); Mhlanga, Sabelo Dalton [Department of Applied Chemistry, University of Johannesburg, PO Box 17011, Doornfontein, 2028 Johannesburg (South Africa); Coville, Neil John [Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand, Private Bag 3, Wits, 2050 Johannesburg (South Africa); DST/NRF Centre of Excellence in Strong Materials, University of the Witwatersrand, Private Bag 3, Wits, 2050 Johannesburg (South Africa)

    2014-11-15

    Nickel sulphide (NiS) nanostructures decorated with gold (Au) nanoparticles (NPs) were synthesized via a microwave-assisted hydrothermal technique. Binary phase NiS (α and β) crystalline nanostructures, bare, and decorated with Au NPs were obtained and confirmed by X-ray diffraction (XRD) studies. TEM analysis revealed that the NiS nanostructures were of various shapes. A quantum confinement effect was confirmed by the blue shift PL emissions and high optical energy band gap observed for the as-synthesized sample. A threefold light emission enhancement due to Au NP coatings was obtained when Au metal NP decoration concentrations was varied from 1% to 10%. These enhancements were attributed to the surface plasmon resonance (SPR) excitation of the surface decorated metal NPs which results in an increased rate of spontaneous emission. The PL enhancement factor was observed to vary at different NiS emissions as well as with the size of the Au NPs. The effect of metal NP decoration on the PL emission of NiS is to the best of our knowledge, presented for the first time. - Highlights: • Binary phase NiS decorated with gold nanoparticles. • Quantum confinement effect confirmed by PL analysis. • PL enhancement depending more on particle size distribution. • Effect of gold on NiS PL is to the best of our knowledge reported for the first time.

  7. Size dependence of structure and magnetic properties of CoCr2O4 nanoparticles synthesized by hydrothermal technique

    Science.gov (United States)

    Tian, Zhaoming; Zhu, Changming; Wang, Junfeng; Xia, Zhengcai; Liu, Yong; Yuan, Songliu

    2015-03-01

    The size dependence of structure and magnetic behavior has been investigated on spinel chromite CoCr2O4 nanoparticles (NPs) with different particles from ~2.8 to ~19.7 nm, synthesized by a hydrothermal technique. The microstructure analysis shows that the lattice parameter increases monotonically with reduced particle sizes. Compared with the bulk sample, all synthesized NPs exhibit lower Curie temperature (TC~87 K) from paramagnetic (PM) to collinear short-range ferrimagnetic (FiM) state, and this PM-FiM transition is gradually degraded with decreased particle sizes and nearly vanishes for ~2.8 nm NPs. No magnetic transition from short-range FiM order to long-range spiral spin structure is found at low temperatures contrast to the bulk ones. Instead, a cluster spin-glass (SG) transition appears for NPs with D≤5.4 nm. The dynamic behavior of the cluster SG can be described by a power law with the spin relaxation time in the range of 10-10-10-8 s and critical exponent zv‧=9.9±0.6, in accordance with a three-dimensional Ising SG behavior. The glass transition temperature (Tg) decreases from 16.3 K for ~5.4 nm to 12.8 K for ~2.8 nm NPs.

  8. Size-dependent and intra-band photoluminescence of NiS2 nano-alloys synthesized by microwave assisted hydrothermal technique

    CSIR Research Space (South Africa)

    Linganiso, C

    2013-03-01

    Full Text Available Journal of Alloys and Compounds March 2013/ Vol 552, pp 345-350 Size-dependent and intra-band photoluminescence of NiS2 nano- alloys synthesized by microwave assisted hydrothermal technique Ella Cebisa Linganiso a,b, Sabelo Dalton Mhlanga b...

  9. Optical and morphological properties of ZnO- and TiO2-derived nanostructures synthesized via a microwave-assisted hydrothermal method

    CSIR Research Space (South Africa)

    Moloto, N

    2012-01-01

    Full Text Available A microwave-assisted hydrothermal method was used to synthesize ZnO and TiO2 nanostructures. The experimental results show that the method resulted in crystalline monodispersed ZnO nanorods that have pointed tips with hexagonal crystal phase. TiO2...

  10. Magnetic and Structural Properties of Cobalt- and Zinc-Substituted Nickel Ferrite Synthesized by Microwave-Assisted Hydrothermal Method

    Science.gov (United States)

    Sinfrônio, F. S. M.; Santana, P. Y. C.; Coelho, S. F. N.; Silva, F. C.; de Menezes, A. S.; Sharma, S. K.

    2017-02-01

    Ceramic spinel-based ferrites of cobalt, nickel and zinc were prepared by means of the microwave-assisted hydrothermal method. All samples were thoroughly characterized using different techniques for their structural, compositional, phonic and magnetic properties. The Rietveld analysis of x-ray powder diffraction data revealed the crystallinity as well single-phase partially inverse spinel structure. Wavelength dispersive x-ray fluorescence measurement indicates a good correlation between the empirical stoichiometry. The estimated average crystallite size varies between 9 nm and 13 nm (XRPD) and 6 and 14 nm for high-resolution transmission electron microscopy measurements. In addition, the observed micro-strain varies in the range of 0.01-0.6%. All samples show a quasi-spherical morphology and slight agglomeration. Infrared and Raman data spectra exhibit characteristic modes for spinel-based ferrites. Direct current magnetic measurements indicate behavior typical of magnetically soft materials system at 300 K.

  11. Hydrothermal synthesis of nanostructured graphene/polyaniline composites as high-capacitance electrode materials for supercapacitors

    Science.gov (United States)

    Wang, Ronghua; Han, Meng; Zhao, Qiannan; Ren, Zonglin; Guo, Xiaolong; Xu, Chaohe; Hu, Ning; Lu, Li

    2017-03-01

    As known to all, hydrothermal synthesis is a powerful technique for preparing inorganic and organic materials or composites with different architectures. In this reports, by controlling hydrothermal conditions, nanostructured polyaniline (PANi) in different morphologies were composited with graphene sheets (GNS) and used as electrode materials of supercapacitors. Specifically, ultrathin PANi layers with total thickness of 10-20 nm are uniformly composited with GNS by a two-step hydrothermal-assistant chemical oxidation polymerization process; while PANi nanofibers with diameter of 50~100 nm are obtained by a one-step direct hydrothermal process. Benefitting from the ultrathin layer and porous structure, the sheet-like GNS/PANi composites can deliver specific capacitances of 532.3 to 304.9 F/g at scan rates of 2 to 50 mV/s. And also, this active material showed very good stability with capacitance retention as high as ~99.6% at scan rate of 50 mV/s, indicating a great potential for using in supercapacitors. Furthermore, the effects of hydrothermal temperatures on the electrochemical performances were systematically studied and discussed.

  12. Hydrothermal synthesis of nanostructured graphene/polyaniline composites as high-capacitance electrode materials for supercapacitors

    Science.gov (United States)

    Wang, Ronghua; Han, Meng; Zhao, Qiannan; Ren, Zonglin; Guo, Xiaolong; Xu, Chaohe; Hu, Ning; Lu, Li

    2017-01-01

    As known to all, hydrothermal synthesis is a powerful technique for preparing inorganic and organic materials or composites with different architectures. In this reports, by controlling hydrothermal conditions, nanostructured polyaniline (PANi) in different morphologies were composited with graphene sheets (GNS) and used as electrode materials of supercapacitors. Specifically, ultrathin PANi layers with total thickness of 10–20 nm are uniformly composited with GNS by a two-step hydrothermal-assistant chemical oxidation polymerization process; while PANi nanofibers with diameter of 50~100 nm are obtained by a one-step direct hydrothermal process. Benefitting from the ultrathin layer and porous structure, the sheet-like GNS/PANi composites can deliver specific capacitances of 532.3 to 304.9 F/g at scan rates of 2 to 50 mV/s. And also, this active material showed very good stability with capacitance retention as high as ~99.6% at scan rate of 50 mV/s, indicating a great potential for using in supercapacitors. Furthermore, the effects of hydrothermal temperatures on the electrochemical performances were systematically studied and discussed. PMID:28291246

  13. Applications versus properties of Mg–Al layered double hydroxides provided by their syntheses methods: Alkoxide and alkoxide-free sol–gel syntheses and hydrothermal precipitation

    KAUST Repository

    Chubar, Natalia

    2013-12-01

    A tremendous number of studies have examined layered double hydroxides (LDH) for their technological applications in the ion exchange removal of toxic ions, recovery of valuable substances, catalysis, CO2 capture, as a layered host for storage/delivery of biologically active molecules, additives to plastics and building materials, and other functions. Numerous publications always conclude that the materials (prepared, as a rule, using the oldest synthesis method) are very promising for each investigated application; however, the main chemical industries producing these materials advertise them mainly (or only) as plastic additives. The authors performed extensive research using many of the appropriate methods to compare the structure, surface and adsorptive properties of three Mg-Al LHDs produced by advanced synthesis methods. One industrial sample (by Sasol, Germany) prepared by the alkoxide sol-gel method and two novel Mg-Al LDHs synthesised in-house by alkoxide-free sol-gel and hydrothermal precipitation approaches were investigated. Reasons for the very different adsorptive selectivity of the three LDHs towards arsenate, selenate, phosphate, arsenite and selenite have been provided, highlighting the role of speciation of the interlayer carbonate, aluminium, magnesium, interlayer hydration and moisture content in the adsorptive selectivity towards each toxic anion. This work is the first report presenting the regularities of the LDHs structure, surface and anion exchange properties as a function of their syntheses method. It establishes the links to potential technological applications of each investigated LDH and explains the necessary properties required to make the technological application cost-effective and efficient. The paper might accelerate industrial applications of these advanced materials. © 2013 Elsevier B.V.

  14. Structural and optical characterization and efficacy of hydrothermal synthesized Cu and Ag doped zinc oxide nanoplate bactericides

    Energy Technology Data Exchange (ETDEWEB)

    Abinaya, C.; Marikkannan, M.; Manikandan, M. [Department of Materials Science, School of Chemistry, Madurai Kamaraj University, Madurai, 625 021, Tamil Nadu (India); Mayandi, J., E-mail: jeyanthinath@yahoo.co.in [Department of Materials Science, School of Chemistry, Madurai Kamaraj University, Madurai, 625 021, Tamil Nadu (India); Department of Materials Science and Engineering, Michigan Technological University, Houghton, 49931 1295, MI (United States); Suresh, P.; Shanmugaiah, V. [Department of Microbial Technology, School of Biological Sciences, Madurai Kamaraj University, Madurai, 625 021, Tamil Nadu (India); Ekstrum, C. [Department of Materials Science and Engineering, Michigan Technological University, Houghton, 49931 1295, MI (United States); Pearce, J.M. [Department of Materials Science and Engineering, Michigan Technological University, Houghton, 49931 1295, MI (United States); Department of Electrical & Computer Engineering, Michigan Technological University, Houghton, 49931 1295, MI (United States)

    2016-12-01

    This study reports on a novel synthesis of pure zinc oxide and both Cu and Ag doped ZnO nanoplates using a simple and low-cost hydrothermal method. The structural and optical properties of the nanoplates were quantified and the materials were tested for antibacterial activity. X-ray diffraction revealed the formation of the wurtzite phase of ZnO and scanning and transmission electron microscopy showed the formation of randomly oriented ZnO nanoplates, having a thickness less than 80 nm and diameter less than 350 nm. The elemental analyses of both the pure and doped samples were evaluated by energy dispersive X-ray spectrometry. The FTIR spectra of ZnO nanomaterials showed the predictable bands at 3385 cm{sup −1} (O−H stretching), 1637 cm{sup −1} (stretching vibration of H{sub 2}O), 400 cm{sup −1}–570 cm{sup −1} (M−O stretching). The as synthesized samples showed a strong absorption peak in the UV region (∼376 nm) and a near band edge emission at 392 nm with some defect peaks in the visible region. From the XPS spectra the oxidation states of Zn, Cu and Ag were found to be +2, +2 and 0 respectively. Escherichia coli, Staphylococcus aureus and Salmonella typhi bacteria were used to evaluate the antibacterial activity of undoped and doped ZnO. Ag doped ZnO exhibited low minimum inhibitory concentration (MIC) values as 40 μg/ml for E. coli and S. aureus and 20 μg/ml for S. typhi, which are comparable to commercial antibiotics without optimization. Further, these chemically modified nanoparticles will be applicable in the development of medicine to control the spread and infection of a variety of bacterial strains. - Highlights: • Distinct ZnO nanoplates were successfully synthesized by facile hydrothermal method. • Cu and Ag doped ZnO exhibits significant destruction of bacteria with low MIC value. • Ag:ZnO has a noteworthy bactericidal effect against E. coli, S. aureus &S. typhi. • It projects that, a feasible low cost industrial process can

  15. Hydrothermal synthesis and characterization of hybrid Al/ZnO-GO composite for significant photodegrdation of dyes

    Science.gov (United States)

    Lellala, Kashinath; Namratha, K.; Sudhakar, K.; Byrappa, K.

    2016-05-01

    In the present work, undoped and doped Aluminum/Zinc Oxide - graphene oxide (Al/ZnO-GO) nanocomposite have been successfully synthesized by hydrothermal method from zinc acetate and aluminum nitrate solutions without using of any surfactant/stabilizing agents. The results show that the composites of GO nanosheets are decorated densely by Al/ZnO nanoparticles, which displays a good morphology and blend between GO and Al/ZnO. Hybrid composites exhibit an enhanced photocatalytic performance in reduction of dyes under UV-Vis radiation better than bare ZnO-GO and GO for methylene blue dye. The hydrothermal method leads to particles with a higher crystalline due to ambient temperature of the reaction and autogenously pressure conditions, which alters the phases and crystallizations of the nanocomposite. The optical band gap is narrowed to lower energy values due to controlled addition of aluminum and GO in the composite. The improved optical property in Al-doped ZnO flower decorated on GO can be attributed to the decrease in oxygen deficiency after Al doping. XRD, FTIR, UV-Vis spectroscopy, Raman, and Field Emission Scanning Electron Microscopy characterized the effects of Al doping on the structural characteristics and optical properties on the ZnO-GO.

  16. Hydrothermal synthesis and characterization of hybrid Al/ZnO-GO composite for significant photodegrdation of dyes

    Energy Technology Data Exchange (ETDEWEB)

    Lellala, Kashinath; Namratha, K.; Byrappa, K., E-mail: kashinathlellala@gmail.com, E-mail: kbyrappa@gmail.com [Centre for Materials Science and Technology, University of Mysore, Vijnana Bhavan, P.B.No.21, Manasagangothri, Mysore - 570006, India. (India); Sudhakar, K. [Lal Bhadur College, S.V.N. Road, Mulugu X-road, Kakatiya University, Warangal-560001, India. (India)

    2016-05-06

    In the present work, undoped and doped Aluminum/Zinc Oxide - graphene oxide (Al/ZnO-GO) nanocomposite have been successfully synthesized by hydrothermal method from zinc acetate and aluminum nitrate solutions without using of any surfactant/stabilizing agents. The results show that the composites of GO nanosheets are decorated densely by Al/ZnO nanoparticles, which displays a good morphology and blend between GO and Al/ZnO. Hybrid composites exhibit an enhanced photocatalytic performance in reduction of dyes under UV-Vis radiation better than bare ZnO-GO and GO for methylene blue dye. The hydrothermal method leads to particles with a higher crystalline due to ambient temperature of the reaction and autogenously pressure conditions, which alters the phases and crystallizations of the nanocomposite. The optical band gap is narrowed to lower energy values due to controlled addition of aluminum and GO in the composite. The improved optical property in Al-doped ZnO flower decorated on GO can be attributed to the decrease in oxygen deficiency after Al doping. XRD, FTIR, UV-Vis spectroscopy, Raman, and Field Emission Scanning Electron Microscopy characterized the effects of Al doping on the structural characteristics and optical properties on the ZnO-GO.

  17. Stable Isotopic Composition for Hydrothermal Vein Deposits, Southeastern Korea

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    @@The southeast of Korea has attracted considerable attention in the geologic community because of its extensive igneous activity and associated mineralizations from the Late Cretaceous to the Early Tertiary (Cu, Pb-Zn, W-Mo, Bi and Au-Ag hydrothermal-vein deposits, porphyry, skarn and altered clay deposits). The southeast of Korea is composed of Cretaceous sedimentary Gyeongsan basin, volcanic and plutonic rocks. Most of the mines are either closed or incapable of producing more ores because of their poor reserves. The south of the Gyeongsang basin is famous for its hydrothermal altered clay deposits associated with volcanism. In order to locate more metal resources, many researches have been conducted into the gold-silver mineralization within hydrothermai-altered deposits in the past several years. The age of plutonism ranges from 112 Ma to 44 Ma, and that of volcanism from 74 Ma to 47 Ma.

  18. Flexible composite via rapid titania coating by microwave-assisted hydrothermal synthesis

    Indian Academy of Sciences (India)

    RICARDO MARQUES E SILVA; ANDERSON THESING; VINICIUS GONÇALVES DEON; ALICE GONÇALVES OSÓRIO; BRUNO DA SILVEIRA NOREMBERG; NATÁLIA HADLER MARINS; MARCELO ORNAGHI ORLANDI; FABIANA VILLELA DA MOTTA; RUBENS MARIBONDO DO NASCIMENTO; NEFTALI LENIN VILLARREAL CARREÑO

    2017-06-01

    The aim of this work was to prepare a flexible nanocomposite from ultra-fine titanium oxide (TiO$_2$) growth on carbon fibre via microwave-assisted hydrothermal synthesis (MHS) and to evaluate its photocatalytic properties. The TiO$_2$ nanoparticles were directly grown on the carbon fibre (CF). Thus, a study comparing the conventional titania coating vs. the MHS were performed. The significant layer interaction as a function of the coating method on the visible and dark dye photodegradation performance was observed. Techniques such as X-ray diffraction, electron microscopy (field-emission scanning electron microscope (FESEM)), Raman spectroscopy, among others were used aiming to characterize the different route samples. This study reports a reproducible and single method to manufacture of nanocomposites through the growth ofTiO$_2$ nanoparticle on CF by MHS that allow controlling the thickness layer. Similar procedure of synthesized nanocomposite could be applied in different chemical compositions to advanced applications, based on the electrochemical nanostructure.

  19. ZnS/Ni{sub 2}P core/shell composites: Simple hydrothermal synthesis, characterization and its photocatalytic degradation of pyronine B

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Shuling, E-mail: shulingliu@aliyun.com [Key Laboratory of Auxiliary Chemistry & Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science & Technology, Xi’an, Shaanxi 710021 (China); College of Chemistry & Chemical Engineering, Shaanxi University of Science & Technology, Xi’an, Shaanxi 710021 (China); Ma, Lanbing; Zhang, Hongzhe; Ma, Chenlu [Key Laboratory of Auxiliary Chemistry & Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science & Technology, Xi’an, Shaanxi 710021 (China); College of Chemistry & Chemical Engineering, Shaanxi University of Science & Technology, Xi’an, Shaanxi 710021 (China)

    2016-05-15

    Highlights: • ZnS/Ni{sub 2}P composites have been firstly synthesized via a gentle hydrothermal route. • The composites have been characterized by XRD, SEM and TEM. • ZnS/Ni{sub 2}P showed enhanced photocatalytic degradation activity for pyronine B. • The reason for the enhanced photocatalytic activity has been discussed. - Abstract: ZnS/Ni{sub 2}P core/shell composites were successfully synthesized using a hydrothermal method. The composites have been characterized by XRD, SEM, TEM and the corresponding results showed that the composites were composed of the cubic ZnS microspheres, which were made up of ZnS nanoparticles, and Ni{sub 2}P nanoparticles coated on the surfaces of ZnS microspheres. Compared with ZnS microspheres, ZnS/Ni{sub 2}P core/shell composites showed enhanced photocatalytic degradation activity for pyronine B under UV irradiation. This may be related to the effective separation of photogenerated electron–hole pairs in ZnS/Ni{sub 2}P composites which can greatly reduce the chance of their recombination. Furthermore, superoxide ions and hydroxyl radical can be more easily produced through ZnS/Ni{sub 2}P composites, which is also beneficial for the degradation of pyronine B.

  20. Adsorption and photocatalytic degradation of methylene blue using high surface area titanate nanotubes (TNT) synthesized via hydrothermal method

    Science.gov (United States)

    Subramaniam, M. N.; Goh, P. S.; Abdullah, N.; Lau, W. J.; Ng, B. C.; Ismail, A. F.

    2017-06-01

    Removal of methylene blue (MB) via adsorption and photocatalysis using titanate nanotubes (TNTs) with different surface areas were investigated and compared to commercial titanium dioxide (TiO2) P25 Degussa nanoparticles. The TNTs with surface area ranging from 20 m2/g to 200 m2/g were synthesized via hydrothermal method with different reaction times. TEM imaging confirmed the tubular structure of TNT while XRD spectra indicated all TNTs exhibited anatase crystallinity. Batch adsorption rate showed linearity with surface properties of TNTs, where materials with higher surface area showed higher adsorption rate. The highest MB adsorption (70%) was achieved by TNT24 in 60 min whereas commercial TiO2 exhibited the lowest adsorption of only 10% after 240 min. Adsorption isotherm studies indicated that adsorption using TNT is better fitted into Langmuir adsorption isotherm than Freundlich isotherm model. Furthermore, TNT24 was able to perform up to 90% removal of MB within 120 min, demonstrating performance that is 2-fold better compared to commercial TiO2. The high surface area and surface Bronsted acidity are the main reasons for the improvement in MB removal performance exhibited by TNT24. The improvement in surface acidity enhanced the adsorption properties of all the nanotubes prepared in this study.

  1. Field-emission characteristics of Al-doped ZnO nanostructures hydrothermally synthesized at low temperature.

    Science.gov (United States)

    Yang, Po-Yu; Wang, Jyh-Liang; Tsai, Wei-Chih; Wang, Shui-Jinn; Lin, Jia-Chuan; Lee, I-Che; Chang, Chia-Tsung; Cheng, Huang-Chung

    2011-07-01

    The aluminum-doped ZnO (AZO) nanostructures with different Al concentrations were synthesized on AZO/glass substrate via a simple hydrothermal growth method at a temperature as low as 85 degrees C. The morphologies, crystallinity, optical emission properties, and chemical bonding states of AZO nanostructures show evident dependence on the aluminum dosage. The morphologies of AZO nanostructures were changed from vertically aligned nanowires (NWs), and NWs coexisted with nanosheets (NSs), to complete NSs in respect of the Al-dosages of 0-3 at.%, 5 at.%, and 7 at.%, correspondingly. The undoped ZnO and lightly Al-doped AZO (< or = 3 at.%) NWs are single-crystalline wurtzite structure. In contrast, heavily Al-doped AZO sample is polycrystalline. The AZO nanostructure with 3 at.% Al-dosages reveals the optimal crystallinity and less structural defects, reflecting the longest carrier lifetime and highest conductivity. Consequently, the field-emission characteristics of such an AZO emitter can exhibit the higher current density, larger field-enhancement factor (beta) of 3131, lower turn-on field of 2.17 V/microm, and lower threshold field of 3.43 V/microm.

  2. Emulsion-templated macroporous carbons synthesized by hydrothermal carbonization and their application for the enzymatic oxidation of glucose.

    Science.gov (United States)

    Brun, Nicolas; Edembe, Lise; Gounel, Sébastien; Mano, Nicolas; Titirici, Magdalena M

    2013-04-01

    Carbon-based monoliths have been designed using a simple synthetic pathway based on using high internal phase emulsion (HIPE) as a soft template to confine the polymerization and hydrothermal carbonization of saccharide derivatives (furfural) and phenolic compounds (phloroglucinol). Monosaccharides can be isolated from the cellulosic fraction of lignocellulosic biomass and phloroglucinol can be extracted from the bark of fruit trees; however, this approach constitutes an interesting sustainable synthetic route. The macroscopic characteristics can be easily modulated; a high macroporosity and total pore volume of up to 98 % and 18 cm(3)g(-1) have been obtained, respectively. After further thermal treatment under inert atmosphere, the as-synthesized macroporous carbonized HIPEs (carbo-HIPEs) have shaping capabilities relating to interesting mechanical properties as well as a high electrical conductivity of up to 300 Sm(-1) . These conductive foams exhibit a hierarchical structure associated with the presence of both meso- and micropores that exhibit specific Brunauer-Emmett-Teller (BET) surface areas and DFT total pore volumes up to 730 m(2)g(-1) and 0.313 cm(3)g(-1) , respectively. Because of their attractive structural characteristics and intrinsic properties, these macroporous monoliths have been incorporated as a proof of principle within electrochemical devices as modified thin carbon disc electrodes. A promising two-fold improvement in the catalytic current is observed for the electrooxidation of glucose after the immobilization of a glucose oxidase-based biocatalytic mixture onto the carbo-HIPE electrodes compared to that observed if using commercial glassy carbon electrodes.

  3. Effect of organic additives on characteristics of carbon-coated LiCoPO4 synthesized by hydrothermal method

    Science.gov (United States)

    Maeyoshi, Yuta; Miyamoto, Shohei; Noda, Yusaku; Munakata, Hirokazu; Kanamura, Kiyoshi

    2017-01-01

    Carbon-coated LiCoPO4 particles are synthesized by one-pot hydrothermal process using three different organic additives (carboxymethylcellulose sodium salt (CMC), glucose, and ascorbic acid). The effect of the organic additives on particle size, morphology, nature of carbon coating, and electrochemical property of the resulting LiCoPO4 is investigated. CMC plays important roles to decrease the particle size and form well-covered carbon coating on the surface. Carbon-coated LiCoPO4 prepared using CMC delivers higher initial discharge capacity of 135 mA h g-1 at 0.1 C, and shows superior rate capability and cyclic performance than the other samples. The improved electrochemical characteristics are attributed to not only the fine particle which allows facile electronic and ionic transport, but also the high coverage of carbon coating which improves the electrical conductivity and prevents the irreversible reactions of the charged LiCoPO4 with electrolyte.

  4. Studies on the Fe3+ Doping Effect on Structural, Optical and Catalytic Properties of Hydrothermally Synthesized TiO2 Photocatalyst

    Energy Technology Data Exchange (ETDEWEB)

    Kamble, Ravi [Department of Physics, Jaysingpur College, Jaysingpur-416101, India; Sabale, Sandip [P.G. Department of Chemistry, Jaysingpur College, Jaysingpur-416101, Maharashtra, India; Chikode, Prashant [Department of Physics, Jaysingpur College, Jaysingpur-416101, India; Puri, Vijaya [Department of Physics, Shivaji University, Kolhapur-416004, India; Yu, Xiao-Ying [Earth and Biological Sciences Directorate, Pacific Northwest National Laboratory (PNNL), Richland, WA 99352, United States; Mahajan, Smita [Department of Physics, Jaysingpur College, Jaysingpur-416101, India

    2017-08-01

    Pure TiO2 and Fe3+-TiO2 nanoparticles have been prepared by simple hydrothermal method with different Fe3+ concentrations. The synthesized nanoparticles are analysed to determine its structural, optical, morphological and compositional properties using X-ray diffraction, Raman, UV-DRS, photoluminescence, Mossbauer, XPS, TEM and SEM/EDS. The EDS micrograph confirms the existence of Fe3+ atoms in the TiO2 matrix with 0.85, 1.52 and 1.87 weight percent. The crystallite size and band gap decrease with increase in Fe3+concentration. The average particle size obtained from TEM is 7-11 nm which is in good agreement with XRD results. Raman bands at 640 cm-1, 517 cm-1 and 398 cm-1 further confirm pure phase anatase in all samples. XPS shows the proper substitutions of few sites of Ti4+ ions by Fe3+ ions in the TiO2 host lattice. The intensity of PL spectra for Fe3+-TiO2 shows a gradual decrease in the peak intensity with increasing Fe3+ concentration in TiO2, and it indicates lower recombination rate as Fe3+ ions increases. These nanoparticles are further studied for its photocatalytic activities using malachite green dye under UV light, visible light and sunlight.

  5. Effect of Synthesizing Temperature on Microstructure and Electrochemical Property of the Hydrothermal Conversion Coating on Mg-2Zn-0.5Mn-Ca-Ce Alloy

    Directory of Open Access Journals (Sweden)

    Guanghui Guo

    2016-02-01

    Full Text Available Mg(OH2 conversion coatings were formed on an Mg-2Zn-0.5Mn-Ca-Ce alloy via hydrothermal method at three different synthesizing temperatures (160, 170 and 180 °C. The effect of synthesizing temperature on microstructure and electrochemical property of the coatings were systematically studied. With increasing synthesizing temperature, the coating became thicker due to the faster reaction and deposition of Mg(OH2 on the α-Mg phase and secondary phases of the substrate Mg alloy. Internal micro-cracks were also generated in the higher-temperature synthesized coatings due to the increased shrinking stress, but the cross-cutting micro-cracks were suppressed. Benefiting from the improved barrier effect against penetration of corrosive medium, the higher-temperature synthesized thicker coating presented significantly enhanced electrochemical property and anti-corrosion efficiency in Hanks’ solution.

  6. One-step synthesis of mesoporous silica–graphene composites by simultaneous hydrothermal coupling and reduction of graphene oxide

    Indian Academy of Sciences (India)

    Juliet Q Dalagan; Erwin P Enriquez

    2014-05-01

    Silica–graphene oxide composites were synthesized by hydrothermal method with simultaneous functionalization and reduction of graphene oxide (GO) in the presence of mesoporous silica. Two types of silica were used in the study, mesoporous synthetic silica (MSU-F) synthesized by sol-gel method and mesoporous mineral silica (meso-celite) from pseudomorphic synthesis. The infrared spectra of the composites showed the disappearance of the carboxyl peak at 1735 cm-1 which could be due to the reduction of the –COOH group. The enhancement of the band at 1385 cm-1 is attributed to the vibration of the Si–O–C=O moiety formed by reaction of the –COOH group of GO and the silanol (Si–OH) of silica. The Raman spectra of the composites show a diminished intensity ratio of D to G band indicating that GO was reduced to graphene sheets. The TEM images demonstrate the coupling of silica to GO surface revealing dense loading of silica on GO in planar structure.

  7. The effect of poly vinyl alcohol (PVA) surfactant on phase formation and magnetic properties of hydrothermally synthesized CoFe{sub 2}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Jalalian, M.; Mirkazemi, S.M., E-mail: mirkazemi@iust.ac.ir; Alamolhoda, S.

    2016-12-01

    Nanoparticles of CoFe{sub 2}O{sub 4} were synthesized by hydrothermal process at 190 °C with and without poly vinyl alcohol (PVA) addition using treatment durations of 1.5–6 h. The synthesized powders were characterized with X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscope (SEM), Field emission scanning electron microscope (FESEM) and vibration sample magnetometer (VSM) techniques. XRD results show presence of CoFe{sub 2}O{sub 4} as the main phase and Co{sub 3}O{sub 4} as the lateral phase in some samples. The results show that in the samples synthesized without PVA addition considerable amount of lateral phase is present after 3 h of hydrothermal treatment while with PVA addition this phase is undetectable in the XRD patterns of the sample synthesized at the same conditions. Microstructural studies represent increasing of particle size with increasing of hydrothermal duration and formation of coarser particles with PVA addition. The highest maximum magnetization (M{sub max}) values in both of the samples that were synthesized with and without PVA addition are about 59 emu/g that were obtained after 4.5 h of hydrothermal treatment. Intrinsic coercive field ({sub i}H{sub c}) value of the sample without PVA addition increases from 210 to 430 Oe. While with PVA addition the {sub i}H{sub c} value changes from 83 Oe to 493 Oe. The mechanism of changes in M{sub max} and {sub i}H{sub c} values has been explained. - Highlights: • Nanoparticles of CoFe{sub 2}O{sub 4} hydrothermally synthesized with and without PVA addition. • PVA addition facilitates formation of single phase cobalt ferrite. • Coarser particles would be obtained with PVA addition. • The highest M{sub max} values in the samples with and without PVA are equal to 59 emu/g. • The highest {sub i}H{sub c} values are equalt to 320 and 493 Oe without and with PVA respectively.

  8. Structural and photocatalytic studies of hydrothermally synthesized Mn2+-TiO2 nanoparticles under UV and visible light irradiation

    Science.gov (United States)

    Kamble, Ravi; Sabale, Sandip; Chikode, Prashant; Puri, Vijaya; Mahajan, Smita

    2016-11-01

    Pure TiO2 and Mn2+-TiO2 nanoparticles have been prepared by simple hydrothermal method with different Mn2+ concentrations. Obtained samples were analysed to determine it’s structural, optical, morphological and compositional properties using x-ray diffraction, UV-DRS, Raman, photoluminescence, XPS, TEM and EDS analysis. The EDS micrograph confirms the existence of Mn2+ atoms in TiO2 matrix with 0.86, 1.60 and 1.90 wt%. The crystallite size as well as band gap decreases with increase in Mn2+ concentration. The average particle size obtained from TEM was found 8-11 nm which is in good agreement with XRD results. Raman bands at 640, 518 and 398 cm-1 further confirmed pure phase anatase in all samples. XPS shows the proper substitutions of few sites of Ti4+ ions by Mn2+ ions in the TiO2 host lattice. The intensity of PL spectra for Mn2+-TiO2 shows a gradual decrease in the peak intensity with increasing Mn2+ concentration in TiO2, it implies lower electron-hole recombination rate as Mn2+ ions increases. The obtained samples were further studied for its photocatalytic activities using malachite green dye under UV light and visible light.

  9. Improved Electrochemical Performance of Orthorhombic LiMn1-xCrxO2 Synthesized by Hydrothermal Method

    Institute of Scientific and Technical Information of China (English)

    Xiaoyan TU; Guanglie LU; Yuewu ZENG

    2006-01-01

    Single phase chromium-substituted orthorhombic LiMn1-xCrxO2 (0≤x≤0.05) were successfully synthesized by hydrothermal treatment of Mn2O3, Cr2O3 and lithium hydroxide aqueous solution. Structure and morphologies of the o-LiMn1-xCrxO2 were characterized by X-ray diffraction and transmission electron microscopy.Compared to the particle size of o-LiMnO2 ranging from 50 to 150 nm, the Cr-doped one is larger with about 500 nm, which is agglomerated by small grains. There are high stacking faults in nanosized grains that cause easier phase transformation from the orthorhombic to the spinel-like structure on cycling. High-resolution transmission electron microscopy image analysis of electrochemically cycled o-LiMn1-xCrxO2 (x=0, 0.05)samples showed that the nanodomain structure in o-LiMn0.95Cr0.05O2 was comparatively perfect to that in o-LiMnO2. Particle agglomeration and the relatively perfect crystal structure are two key factors for improving cycle performance of o-LiMn0.95Cr0.05O2. The obtained o-LiMn0.95Cr0.05O2 can reach a maximum discharge capacity of 174 mA·h·g-1 at 0.1 C rate in seventh cycle. The discharge capacity fade rate of the samples decreased with increasing Cr amount. Furthermore, o-LiMn0.95Cr0.05O2 gives a highest discharge capacity of 150 mA·h·g-1 at a high current rate of 0.5 C, and retains 130 mA·h·g-1 after 40 cycles.

  10. Visible light induced bactericidal and photocatalytic activity of hydrothermally synthesized BiVO4 nano-octahedrals.

    Science.gov (United States)

    Sharma, Rishabh; Uma; Singh, Sonal; Verma, Ajit; Khanuja, Manika

    2016-09-01

    In the present work, monoclinic bismuth vanadate (m-BiVO4) nanostructures have been synthesized via simple hydrothermal method and employed for visible light driven antimicrobial and photocatalytic activity. Morphology (octahedral) and size (200-300nm) of the m-BiVO4 are studied using transmission electron microscopy (TEM). The crystal structure of m-BiVO4 (monoclinic scheelite structure) is confirmed by high resolution-TEM (HRTEM) and X-ray diffraction (XRD) studies. The band gap of m-BiVO4 was estimated to be ca. 2.42eV through Kubelka-Munk function F(R∞) using diffuse reflectance spectroscopy (DRS). Antimicrobial action of m-BiVO4 is anticipated by (i) shake flask method, (ii) MTT [3-(4,5-Dimethylthiazol-2-Yl)-2,5-Diphenyltetrazolium Bromide] assay for cytotoxicity. SEM analysis has been carried on Escherichia coli (E.coli) before and after treatment with nanostructure materials to reveal the mechanism underlying the antimicrobial action. Antimicrobial activity is studied as a function of m-BiVO4 concentration viz. 20, 40, 60 and 80ppm. The bacterial growth is decreased 80% to 96%, with the increase in m-BiVO4 concentration from 20ppm to 80ppm, respectively, in 2h. Photocatalytic activity and rate kinetics of m-BiVO4 nanostructures have been studied as a function of time on methylene blue (MB) dye degradation which is one of the waste products of textile industries and responsible for water pollution.

  11. Electromagnetic properties of nanocrystalline Al$^{3+}$ substituted MgCuMn ferrites synthesized by microwave hydrothermal method

    Indian Academy of Sciences (India)

    T RAMESH; S R MURTHY

    2016-10-01

    The effect of Al$^{3+}$ substitution on electromagnetic properties has been studied for nanocrystalline Mg$_{0.8}$Cu$_{0.2}Mn$_{0.05}$Al$_x$Fe$_{1.95−x}$O$_4$ ferrites, wherein $x$ varies from 0 to 0.4 in steps of 0.1. These ferrites were synthesizedby using microwave hydrothermal method and then characterized using X-ray diffractometer (XRD), Fourier transform infrared and transmission electron microscopy. The synthesized powders were densified using microwavesintering method at 950◦C/50 min. Structural and surface morphology of sintered samples were characterized using XRD and atomic force microscopy, respectively. The complex permittivity and permeability properties were measuredover a frequency range 100 Hz–1.8 GHz. The temperature variation of magnetic properties were measured in the temperature range of 300–650 K. The electrical and magnetization studies inferred that the values of d.c. resistivity increases by 27%, whereas saturation magnetization decreases linearly from 38.6 to 23.0 emu g$^{−1}$ and Curie temperature was found to be decreased from 628 to 513 K with an increase of Al$^{3+}$ ions. The low dielectric, magnetic losses, moderate saturation magnetization and high-temperature stability properties exhibited by Al$^{3+}$ substituted MgCuMn ferrites make them find applications in microwave devices, such as circulators and isolators etc. The applicability of present samples formicrowave devices has been tested by the measurement of ferromagnetic resonance linewidth at K$_a$ band.

  12. Hydrothermal Synthesis of Metal-Polyphenol Coordination Crystals and Their Derived Metal/N-doped Carbon Composites for Oxygen Electrocatalysis.

    Science.gov (United States)

    Wei, Jing; Liang, Yan; Hu, Yaoxin; Kong, Biao; Zhang, Jin; Gu, Qinfen; Tong, Yuping; Wang, Xianbiao; Jiang, San Ping; Wang, Huanting

    2016-09-26

    Cobalt (or iron)-polyphenol coordination polymers with crystalline frameworks are synthesized for the first time. The crystalline framework is formed by the assembly of metal ions and polyphenol followed by oxidative self-polymerization of the organic ligands (polyphenol) during hydrothermal treatment in alkaline condition. As a result, such coordination crystals are even partly stable in strong acid (such as 2 m HCl). The metal (Co or Fe)-natural abundant polyphenol (tannin) coordination crystals are a renewable source for the fabrication of metal/carbon composites as a nonprecious-metal catalyst, which show high catalytic performance for both oxygen reduction reaction and oxygen evolution reaction. Such excellent performance makes metal-polyphenol coordination crystals an efficient precursor to fabricate low-cost catalysts for the large-scale application of fuel cells and metal-air batteries.

  13. Effects of MAPP Compatibilization and Acetylation Treatment Followed by Hydrothermal Aging on Polypropylene Alfa Fiber Composites

    Directory of Open Access Journals (Sweden)

    Noura Hamour

    2015-01-01

    Full Text Available This work investigates the effect of hydrothermal aging on the properties of polypropylene/alfa fiber composites. Hydrothermal aging was induced in an environmental testing chamber at 65°C and 75% relative humidity (RH over a 1000 h period. At the beginning (t=0 h, the results showed that Young’s moduli of the untreated alfa fibers and the acetylation-treated fibers increased by 21% and 36%, respectively, compared with the virgin polypropylene (PP. Additionally, Young’s moduli decreased by 7% for the compatibilized composites composed of maleic anhydride grafted polypropylene (MAPP. After 1000 h of aging, Young’s moduli decreased by 36% for untreated alfa fibers and 29% for the acetylation-treated alfa fibers and the compatibilized composites. Significant degradation was observed in the untreated alfa fiber samples. The Fourier transformed infrared (FTIR allows us to distinguish the characteristic absorption bands of the main chemical functions present in the composite material before and after aging. The thermal properties showed that the thermal stability and the degree of crystallinity of the composites decreased after hydrothermal aging; this result was corroborated by the dynamical mechanical analysis (DMA results.

  14. Evaluating the Consequences of Edifice Instability-Related Processes in Hydrothermal Ore Genesis at Composite Volcanoes

    Science.gov (United States)

    Szakacs, A.

    2009-05-01

    Composite volcanoes intrinsically evolve toward instability, which is resolved through sudden (e.g. flank/edifice failure) or gradual (e.g. volcano-basement interaction) processes. They commonly host hydrothermal systems and related ore deposits within their edifices and shallow basement. The nature and extent of the influence instability-related processes exert on these hydrothermal systems and ore genesis are as yet poorly understood. Short-term effects are basically related to sudden depressurization of the system. The key factors determining the response of the hydrothermal system are its depth and maturity, and amount of depressurization. Deep excavation will lead to evisceration of the edifice-hosted hydrothermal system, dispersion of its volatiles in the atmosphere and incorporation of solid-phase components in the resulting debris avalanche deposit (DAD). When mature, such a system may provide DAD-hosted ore deposits. The fate of the deeper, basement-hosted hydrothermal system depends on its maturity. The evolution of an immature system will be aborted as a consequence of premature depressurization-driven boiling, and no ore-grade mineralization forms. Mature systems, however, will benefit from pressure drop and induced boiling by massive deposition of pressure-sensitive ore minerals and formation of high-grade ore. Long-range effects of edifice-failure are related to increase of the meteoric input into the hydrothermal system due to the formation of a large depression and reorganization of the surface hydrologic regime. Shift from high-T vapor-dominated regime to low-T dilute hydrothermal regime is its expected outcome. The influence of gradual release of edifice instability by volcano spreading and related phenomena on the hydrothermal system has not been studied so far. Deformation induced in both edifice and basement would result in change of fluid pathways according to the shift of local stress regimes between compressional and tensional, in turn

  15. Chemical Strategies for Template Syntheses of Composite Micro and Nanostructures.

    Science.gov (United States)

    2007-11-02

    syntheses can be accomplished within the pores of the alumina templates to make semiconductor tubules (27). Figure 5 shows that Ti02 tubules prepared...surface area forms have higher photo efficiencies (28). Ti02 /conductor nanocomposites may prove to be useful photocatalysts because the template...synthesized Ti02 nanostructures have very high surface areas (27). Furthermore, as discussed previously, each outer tubular Ti02 catalyst particle has

  16. Characteristics of Sr, Nd and Pb isotopic compositions of hydrothermal Si-Fe-Mn-oxyhydroxides at the PACMANUS hydrothermal field, Eastern Manus Basin

    Institute of Scientific and Technical Information of China (English)

    YANG Baoju; ZENG Zhigang; WANG Xiaoyuan

    2015-01-01

    Si-Fe-Mn-oxyhydroxides dredged at the PACMANUS (Papua New Guinea–Australia–Canada–Manus) hydrothermal field, Eastern Manus Basin, have87Sr/86Sr=0.708 079–0.708 581;εNd=5.149 833–6.534 826;208Pb/204Pb=38.245–38.440;207Pb/204Pb=15.503–15.560;206Pb/204Pb=18.682–18.783.87Sr/86Sr isotope ratios are relatively homogeneous and close to the value of the surrounding seawater (0.709 16). The content of Sr in the samples contributed by seawater was estimated to be 76.7%–83.1% of total amount. The mixing temperature of hydrothermal fluids and seawater were ranging from 53.2°C to 72.2°C and the hydrothermal activities were unstable when the samples precipitated. TheεNd values of all the samples are positive, which differ from the values of ferromanganese nodules (crusts) with hydrogenic origin. Nd was mainly derived from substrate rocks leached by hydrothermal circulation and preserved the hydrothermal signature. Pb isotopic compositions of most samples show minor variability except Sample #9–2 that has relatively high values of Pb isotopes. The Pb may be derived from the Eastern Manus Basin rocks leached by the hydrothermal fluid. The slightly lower208Pb/204Pb and 207Pb/204Pb values of the samples indicated that the hydrothermal circulation in PACMANUS was not entire and sufficient, or that hydrothermal circulation had transient changes in the past. Si-Fe-Mn-oxyhydroxides in the samples preserved the heterogeneities of local rocks.

  17. Oxygen vacancy and Ce{sup 3+} ion dependent magnetism of monocrystal CeO{sub 2} nanopoles synthesized by a facile hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Leini [School of Physics and Materials Science, Anhui University, Hefei 230039 (China); Anhui Key Laboratory of Information Materials and Devices, Anhui University, Hefei 230039 (China); Meng, Fanming, E-mail: mrmeng@ahu.edu.cn [School of Physics and Materials Science, Anhui University, Hefei 230039 (China); Anhui Key Laboratory of Information Materials and Devices, Anhui University, Hefei 230039 (China); Key Laboratory of Materials Modification by Laser, Ion and Electron Beams (Dalian University of Technology), Ministry of Education, Dalian 116024 (China)

    2013-09-01

    Graphical abstract: - Highlights: • Monocrystal CeO{sub 2} nanopoles are synthesized by hydrothermal method. • Suitable reaction time is beneficial for the growth CeO{sub 2} nanopoles. • As-synthesized CeO{sub 2} nanopoles show excellent RTFM. • The RTFM can be attributed to the influences of oxygen vacancies and Ce{sup 3+} ions. - Abstract: Monocrystal CeO{sub 2} nanopoles of 15–25 nm in diameter and 300–900 nm or more in length were synthesized within 100 h using hydrothermal method with CeCl{sub 3}·7H{sub 2}O as cerium source, NaOH as mineralizer, and ethylenediamine as complexant. The results of XRD and SADE analysis indicate that the as-synthesized CeO{sub 2} samples have the fluorite structure. The band gaps of CeO{sub 2} samples are 0.08–0.38 eV smaller than that of bulk CeO{sub 2}. X-ray photoelectron spectroscopy shows that the concentration of Ce{sup 3+} is higher than 20% for CeO{sub 2} samples. All the as-synthesized CeO{sub 2} samples exhibit the room temperature ferromagnetism (RTFM), and the saturation magnetization (M{sub s}) gradually increases with the increase of E{sub g} up to 2.92 eV and then decreases with E{sub g} increasing more. The highest M{sub s} of 0.167 emu/g is obtained from the CeO{sub 2} nanopoles synthesized within 100 h. The RTFM mechanism of CeO{sub 2} nanopoles has been proposed which can be mainly attributed to the influence of oxygen vacancies and Ce{sup 3+} ions.

  18. Piezoelectric Properties of CuO-Doped (K,Na)NbO3 Lead-Free Ceramics Synthesized with Hydrothermal Powders

    Science.gov (United States)

    Yokouchi, Yuriko; Maeda, Takafumi; Bornmann, Peter; Hemsel, Tobias; Morita, Takeshi

    2013-07-01

    We report the piezoelectric properties of CuO-doped hydrothermal (K,Na)NbO3 ceramics that can be applied as hard-type lead-free piezoelectric ceramics. To date, we have succeeded in synthesizing high-quality KNbO3 and NaNbO3 powders by the hydrothermal method, which is based on an ionic reaction at high temperature (around 210 °C) and pressure. Increasing both the piezoelectric constant d and the mechanical quality factor (Qm) is important for resonance-type piezoelectric devices, such as ultrasonic motors and transformers. CuO doping into hydrothermal (K,Na)NbO3 ceramics was examined to realize hard-type lead-free piezoelectric ceramics. By doping with 1.2 mol % CuO, Qm was increased and the dielectric loss (tan δ) was decreased to 0.5%. The grain size was also influenced by the amount of CuO doping, which indicates that Qm is related to the density. To achieve a higher Qm value, the grain size is required to be less than 5 µm however, excessive CuO doping leads to anomalous grain growth. Optimal piezoelectric properties were obtained for 1.2 mol % CuO-doped (K,Na)NbO3; k31 = 0.32, d31 = -44 pC/N, Qm (radial) = 959, and tan δ= 0.5%. These characteristics showed that CuO doping with hydrothermal powders is effective for obtaining hard-type ceramics, and the mechanical quality factor is more than ten times higher than that of nondoped hydrothermal (K,Na)NbO3 ceramics. Therefore, compared with the conventional solid-state method, we could succeed in obtaining hard-type ceramics by a simple and short process.

  19. Photocatalytic Degradation of Rhodamine B Dye with High Purity Anatase Nano-TiO2 Synthesized by a Hydrothermal Method

    Institute of Scientific and Technical Information of China (English)

    SHI Xiaoliang; YANG Xingyong; WANG Shuwei; WANG Sheng; ZHANG Qiaoxin; WANG Yufu

    2011-01-01

    High purity anatase nano-TiO2 powders with high photocatalytic activity were prepared by a hydrothermal synthesis method.X-ray diffraction(XRD),field emission transmission electron microscopy (FETEM),ultraviolet-visible(UV-Vis)light absorption spectrum and photoluminescence(PL)spectrum were adopted to characterize the catalyst.Effects of temperature,time and sol concentration of hydrothermal synthesis on particle size and phases were investigated.Photocatalytic activities in the degradation of Rhodamine B Dye were studied.The experimental results indicated that photocatalytic activity of the nano-TiO2 powers was much higher than that of P25(Degussa).

  20. The isotopic composition of dissolved inorganic nitrogen in hydrothermal vent fluids

    Science.gov (United States)

    Lehmann, M. F.; Bourbonnais, A.; Butterfield, D. A.

    2006-12-01

    Hydrothermal vent systems at mid-ocean ridges are sites with rapid rates of biomass production, sustained by chemolithoautotrophic bacteria at the base of the vent community food chains. The exact metabolic pathways, in particular those that involve nitrogen (N), and the rates at which the metabolic reactions take place are poorly constrained. In previous studies, very low 15N/14N ratios have been attributed to strong N isotope fractionation during chemosynthetic assimilation of ammonium. However, actual data on the N isotopic composition of dissolved inorganic N in vent systems, which could provide coherent information on the sources of N during chemolithoautotrophic biosynthesis, do not exist. Furthermore, the fate of hydrothermally discharged ammonium as well as that of nitrate that is mixed in from the ocean water column have not been the focus of much attention. As a consequence, little is known about N-cycle reactions within hydrothermal vent systems. We will present nitrate isotope (15N/14N and 18O/16O) data from various sites at Axial Volcano on the Juan de Fuca ridge. Their integration with nitrate concentration data suggests non-conservative behavior of nitrate along temperature gradients. Highest N and O isotope ratios (7.6 permil and 21.0 permil, respectively) are found in average diffuse fluids (17°C). Elevated N and O isotope ratios were associated with decreased nitrate concentrations and indicate a nitrate consuming process that fractionates both N and O isotopes. The ratio of 15N versus 18O enrichment in residual nitrate is, however, not consistent with previous reports on nitrate N versus O isotope fractionation during denitrification in the suboxic ocean water column, implying anomalous N and O isotope fractionation during denitrification in hydrothermal vent fluids and/or the presence of additional microbially mediated N transformations that affect the N and O isotope composition of the nitrate pool in the Axial hydrothermal vent system in a

  1. Hydrothermal synthesis of layer-controlled MoS2/graphene composite aerogels for lithium-ion battery anode materials

    Science.gov (United States)

    Zhao, Bing; Wang, Zhixuan; Gao, Yang; Chen, Lu; Lu, Mengna; Jiao, Zheng; Jiang, Yong; Ding, Yuanzhang; Cheng, Lingli

    2016-12-01

    Layer-controlled MoS2/graphene aerogels (MoS2/GA) composites are synthesized by a facile hydrothermal route, in which few-layer (5-15 layers) MoS2 nanosheets with high crystalline are decorated on the surface of graphene nanosheets homogeneously and tightly. The number of the MoS2 layers can be easily controlled through adjusting the amount of molybdenum source in the reaction system. Moreover, the growth mechanism of the lay-controlled MoS2/GA composites is proposed. The three-dimensional MoS2/GA with macroporous micro-structure not only shortens the transportation length of electrons and ions, but also restrains the re-stacking of MoS2 effectively, stabilizing the electrode structure during repeated charging/discharging processes. Electrochemical tests demonstrate that this few-layer MoS2/GA composite exhibits a high reversible capacity of 1085.0 mAh g-1 at current density of 100 mA g-1, as well as extraordinarily high cycling stability and rate capability.

  2. Optical and Morphological Properties of ZnO- and TiO2-Derived Nanostructures Synthesized via a Microwave-Assisted Hydrothermal Method

    OpenAIRE

    2012-01-01

    A microwave-assisted hydrothermal method was used to synthesize ZnO and TiO2 nanostructures. The experimental results show that the method resulted in crystalline monodispersed ZnO nanorods that have pointed tips with hexagonal crystal phase. TiO2 nanotubes were also formed with minimum bundles. The mechanism for the formation of the tubes was validated by HRTEM results. The optical properties of both ZnO and TiO2 nanostructures showed characteristics of strong quantum confinement regime. The...

  3. Optical and Morphological Properties of ZnO- and TiO2-Derived Nanostructures Synthesized via a Microwave-Assisted Hydrothermal Method

    Directory of Open Access Journals (Sweden)

    Nosipho Moloto

    2012-01-01

    Full Text Available A microwave-assisted hydrothermal method was used to synthesize ZnO and TiO2 nanostructures. The experimental results show that the method resulted in crystalline monodispersed ZnO nanorods that have pointed tips with hexagonal crystal phase. TiO2 nanotubes were also formed with minimum bundles. The mechanism for the formation of the tubes was validated by HRTEM results. The optical properties of both ZnO and TiO2 nanostructures showed characteristics of strong quantum confinement regime. The photoluminescence spectrum of TiO2 nanotubes shows good improvement from previously reported data.

  4. Optical Spectroscopy and Visible Upconversion Studies of YVO4:Er3+ Nanocrystals Synthesized by a Hydrothermal Process

    NARCIS (Netherlands)

    Sun, Y.; Liu, H.; Wang, X.; Kong, X.; Zhang, H.

    2006-01-01

    Abstract: Strong visible emissions of Er3+ resulting from two-photon absorption and energy transfer from the host YVO4 were observed in nanocrystalline Er3+-doped YVO4, which was prepared by a hydrothermal method using a citrate-yttrium-vanadate complex as the precursor. The nanocrystals were

  5. Optical Spectroscopy and Visible Upconversion Studies of YVO4:Er3+ Nanocrystals Synthesized by a Hydrothermal Process

    NARCIS (Netherlands)

    Sun, Y.; Liu, H.; Wang, X.; Kong, X.; Zhang, H.

    2006-01-01

    Abstract: Strong visible emissions of Er3+ resulting from two-photon absorption and energy transfer from the host YVO4 were observed in nanocrystalline Er3+-doped YVO4, which was prepared by a hydrothermal method using a citrate-yttrium-vanadate complex as the precursor. The nanocrystals were charac

  6. Composite synvolcanic intrusions associated with Precambrian VMS-related hydrothermal systems

    Science.gov (United States)

    Galley, Alan G.

    2003-06-01

    Large subvolcanic intrusions are recognized within most Precambrian VMS camps. Of these, 80% are quartz diorite-tonalite-trondhjemite composite intrusions. The VMS camps spatially associated with composite intrusions account for >90% of the aggregate sulfide tonnage of all the Precambrian, intrusion-related VMS camps. These low-alumina, low-K, and high-Na composite intrusions contain early phases of quartz diorite and tonalite, followed by more voluminous trondhjemite. They have a high proportion of high silica (>74% SiO2) trondhjemite which is compositionally similar to the VMS-hosting rhyolites within the volcanic host-rock successions. The quartz-diorite and possibly tonalite phases follow tholeiitic fractionation trends whereas the trondhjemites fall within the composition field for primitive crustal melts. These transitional M-I-type primitive intrusive suites are associated with extensional regimes within oceanic-arc environments. Subvolcanic composite intrusions related to the Archean Sturgeon Lake and Noranda, and Paleoproterozoic Snow Lake VMS camps range in volume from 300 to 1,000 km3. Three have a sill morphology with strike lengths between 15 and 22 km and an average thickness between 1,500 and 2,000 m. The fourth has a gross stock-like shape. The VMS deposits are principally restricted to the volcanic strata above the strike length of the intrusions, as are areally extensive, thin exhalite units. The composite intrusions contain numerous internal phases which are commonly clustered within certain parts of the composite intrusion. These clusters underlie eruptive centers surrounded by areas of hydrothermal alteration and which contain most of the VMS deposits. Early quartz-diorite and tonalite phases appear to have intruded in rapid succession. Evidence includes gradational contacts, magma mixing and disequilibrium textures. They appear to have been emplaced as sill-dike swarms. These early phases are present as pendants and xenoliths within later

  7. Hydrothermal synthesis and properties of NiFe2O4@BaTiO3 composites with well-matched interface

    Directory of Open Access Journals (Sweden)

    Jian-Ping Zhou, Li Lv, Qian Liu, Yu-Xiang Zhang and Peng Liu

    2012-01-01

    Full Text Available NiFe2O4@BaTiO3 multiferroic composite particles were produced by a simple hydrothermal method in two steps: preparing NiFe2O4 nanoparticles and then synthesizing core-shell nanocomposites. Multiferroic composite ceramics were sintered from these powders. X-ray diffraction, Raman scattering and energy dispersive x-ray analyses indicated that the core-shell composites with a NiFe2O4 core and BaTiO3 shell were formed in the hydrothermal environment. Different types of sharp interfaces were self-assembled owing to the minimization of direct elastic energy. The saturation magnetization of the composites linearly increased with the NiFe2O4 content while the dielectric constant decreased. A dielectric peak appeared at around 460 °C because of the oxygen vacancies in the BaTiO3 ceramics. It resulted in an enhancement of magnetic permeability in the composites, indicating magnetoelectric coupling that was also observed by direct magnetoelectric measurements.

  8. Microwave-hydrothermal method for the synthesis of composite materials for removal of arsenic from water.

    Science.gov (United States)

    Andjelkovic, Ivan; Jovic, Bojan; Jovic, Milica; Markovic, Marijana; Stankovic, Dalibor; Manojlovic, Dragan; Roglic, Goran

    2016-01-01

    Composite material Zr-doped TiO2, suitable for the removal of arsenic from water, was synthetized with fast and simple microwave-hydrothermal method. Obtained material, Zr-TiO2, had uniform size and composition with zirconium ions incorporated into crystal structure of titanium dioxide. Synthetized composite material had large specific surface area and well-developed micropore and mesopore structure that was responsible for fast adsorption of As(III) and As(V) from water. The influence of pH on the adsorption capacity of arsenic was studied. The kinetics and isotherm experiments were also performed. The treatment of natural water sample containing high concentration of arsenic with composite material Zr-TiO2 was efficient. The concentration of arsenic was reduced to the value recommended by WHO.

  9. Influence of microstructure on hydrothermal corrosion of chemically vapor processed SiC composite tubes

    Science.gov (United States)

    Kim, Daejong; Lee, Ho Jung; Jang, Changheui; Lee, Hyeon-Geun; Park, Ji Yeon; Kim, Weon-Ju

    2017-08-01

    Multi-layered SiC composites consisting of monolithic SiC and a SiCf/SiC composite are one of the accident tolerant fuel cladding concepts in pressurized light water reactors. To evaluate the integrity of the SiC fuel cladding under normal operating conditions of a pressurized light water reactor, the hydrothermal corrosion behavior of multi-layered SiC composite tubes was investigated in the simulated primary water environment of a pressurized water reactor without neutron fluence. The results showed that SiC phases with good crystallinity such as Tyranno SA3 SiC fiber and monolithic SiC deposited at 1200 °C had good corrosion resistance. However, the SiC phase deposited at 1000 °C had less crystallinity and severely dissolved in water, particularly the amorphous SiC phase formed along grain boundaries. Dissolved hydrogen did not play a significant role in improving the hydrothermal corrosion resistance of the CVI-processed SiC phases containing amorphous SiC, resulting in a significant weight loss and reduction of hoop strength of the multi-layered SiC composite tubes after corrosion.

  10. Structural and electrical properties of TiO{sub 2}/ZnO core–shell nanoparticles synthesized by hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Vlazan, P.; Ursu, D.H. [National Institute for Research and Development in Electrochemistry and Condensed Matter, Department of Condensed Matter, 1 Plautius Andronescu St., 300224 Timisoara (Romania); Irina-Moisescu, C. [Faculty of Industrial Chemistry and Environmental Engineering, “Politehnica” University of Timisoara, 6 Vasile Parvan Avenue, 300223 Timisoara (Romania); Miron, I., E-mail: mironiasmina@gmail.com [National Institute for Research and Development in Electrochemistry and Condensed Matter, Department of Condensed Matter, 1 Plautius Andronescu St., 300224 Timisoara (Romania); Sfirloaga, P. [National Institute for Research and Development in Electrochemistry and Condensed Matter, Department of Condensed Matter, 1 Plautius Andronescu St., 300224 Timisoara (Romania); Faculty of Physics, West University of Timisoara, 4 Vasile Parvan Avenue, 300223 Timisoara (Romania); Rusu, E. [Institute of Electronic Engineering and Nanotechnologies, “D. Ghiţu” of the Academy of Sciences of Moldova, Academiei str. 3, Chisinau MD-2028, Academiei str. 3, Chisinau MD-2028 (Moldova, Republic of)

    2015-03-15

    TiO{sub 2}/ZnO core–shell nanoparticles were successfully synthesized by hydrothermal method in two stages: first stage is the hydrothermal synthesis of ZnO nanoparticles and second stage the obtained ZnO nanoparticles are encapsulated in TiO{sub 2}. The obtained ZnO, TiO{sub 2} and TiO{sub 2}/ZnO core–shell nanoparticles were investigated by means of X-ray diffraction, transmission electron microscopy, Brunauer, Emmett, Teller and resistance measurements. X-ray diffraction analysis revealed the presence of both, TiO{sub 2} and ZnO phases in TiO{sub 2}/ZnO core–shell nanoparticles. According to transmission electron microscopy images, ZnO nanoparticles have hexagonal shapes, TiO{sub 2} nanoparticles have a spherical shape, and TiO{sub 2}/ZnO core–shell nanoparticles present agglomerates and the shape of particles is not well defined. The activation energy of TiO{sub 2}/ZnO core–shell nanoparticles was about 101 meV. - Graphical abstract: Display Omitted - Highlights: • TiO{sub 2}/ZnO core–shell nanoparticles were synthesized by hydrothermal method. • TiO{sub 2}/ZnO core–shell nanoparticles were investigated by means of XRD, TEM and BET. • Electrical properties of TiO{sub 2}/ZnO core–shell nanoparticles were investigated. • The activation energy of TiO{sub 2}/ZnO core–shell nanoparticles was about E{sub a} = 101 meV.

  11. Strong quantum confinement effect in Cu{sub 4}SnS{sub 4} quantum dots synthesized via an improved hydrothermal approach

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Yuehui; Ma, Ligang; Yin, Yan; Qian, Xu; Zhou, Guotai; Gu, Xiaomin [National Laboratory of Solid State Microstructures and Photovoltaic Engineering Center, Department of Physics, Nanjing University, Nanjing (China); Liu, Wenchao, E-mail: wcliu@nju.edu.cn [National Laboratory of Solid State Microstructures and Photovoltaic Engineering Center, Department of Physics, Nanjing University, Nanjing (China); Key Laboratory of Flexible Electronics (KLOFE) & Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials - SICAM, Nanjing Tech University - NanjingTech, Nanjing (China); Wu, Xiaoshan, E-mail: xswu@nju.edu.cn [National Laboratory of Solid State Microstructures and Photovoltaic Engineering Center, Department of Physics, Nanjing University, Nanjing (China); Zhang, Fengming [National Laboratory of Solid State Microstructures and Photovoltaic Engineering Center, Department of Physics, Nanjing University, Nanjing (China)

    2016-07-05

    We developed an improved hydrothermal method with water-oil two-phase reaction system to synthesize size-controllable and oil-soluble Cu{sub 4}SnS{sub 4} (CTS) quantum dots (QDs). The water-oil interface played an important role in controlling nuclei process, growth speed, crystal size and size-distribution of CTS QDs. X-ray diffraction, Raman scattering and transmission electron microscopy studies suggested that the formation and growth mechanism of CTS QDs was revealed to involve three steps. The crystallographic orientation of the CTS nanoprism was analyzed in detail. The blue-shift of absorption edge and broadening of Raman bands were observed due to the quantum confinement effect. The exciton Bohr radius of CTS QDs was calculated to be 3.3–5.8 nm by using the first principle calculation. The size dependence of band-gaps of CTS QDs follows the particle-in-a-box effective-mass model. The ability to fabricate high-quality CTS QDs certainly facilitates the solar cell applications. - Highlights: • We develop an improved hydrothermal method to synthesize monodisperse CTS QDs. • The size can be controlled through controlling the oil/water ratio. • The quantum confinement effect is confirmed by experiments and calculation.

  12. One-Pot Hydrothermal Synthesis of Magnetite Prussian Blue Nano-Composites and Their Application to Fabricate Glucose Biosensor

    Directory of Open Access Journals (Sweden)

    Ezzaldeen Younes Jomma

    2016-02-01

    Full Text Available In this work, we presented a simple method to synthesize magnetite Prussian blue nano-composites (Fe3O4-PB through one-pot hydrothermal process. Subsequently, the obtained nano-composites were used to fabricate a facile and effective glucose biosensor. The obtained nanoparticles were characterized using transmission electron microscopy, scanning electron microscopy, Fourier-transform infrared spectroscopy, UV-vis absorbance spectroscopy, cyclic voltammetry and chronoamperometry. The resultant Fe3O4-PB nanocomposites have magnetic properties which could easily controlled by an external magnetic field and the electro-catalysis of hydrogen peroxide. Thus, a glucose biosensor based on Fe3O4-PB was successfully fabricated. The biosensor showed super-electrochemical properties toward glucose detection exhibiting fast response time within 3 to 4 s, low detection limit of 0.5 µM and wide linear range from 5 µM to 1.2 mM with sensitivity of 32 µA∙mM−1∙cm−2 and good long-term stability.

  13. Fabrication of zirconia composite membrane by in-situ hydrothermal technique and its application in separation of methyl orange.

    Science.gov (United States)

    Kumar, R Vinoth; Ghoshal, Aloke Kumar; Pugazhenthi, G

    2015-11-01

    The main objective of the work was preparation of zirconia membrane on a low cost ceramic support through an in-situ hydrothermal crystallization technique for the separation of methyl orange dye. To formulate the zirconia film on the ceramic support, hydrothermal reaction mixture was prepared using zirconium oxychloride as a zirconia source and ammonia as a precursor. The synthesized zirconia powder was characterized by X-ray diffractometer (XRD), N2 adsorption/desorption isotherms, Thermogravimetric analysis (TGA), Fourier transform infrared analysis (FTIR), Energy-dispersive X-ray (EDX) analysis and particle size distribution (PSD) to identify the phases and crystallinity, specific surface area, pore volume and pore size distribution, thermal behavior, chemical composition and size of the particles. The porosity, morphological structure and pure water permeability of the prepared zirconia membrane, as well as ceramic support were investigated using the Archimedes' method, Field emission scanning electron microscopy (FESEM) and permeability. The specific surface area, pore volume, pore size distribution of the zirconia powder was found to be 126.58m(2)/g, 3.54nm and 0.3-10µm, respectively. The porosity, average pore size and pure water permeability of the zirconia membrane was estimated to be 42%, 0.66µm and 1.44×10(-6)m(3)/m(2)skPa, respectively. Lastly, the potential of the membrane was investigated with separation of methyl orange by means of flux and rejection as a function of operating pressure and feed concentration. The rejection was found to decrease with increasing the operating pressure and increases with increasing feed concentrations. Moreover, it showed a high ability to reject methyl orange from aqueous solution with a rejection of 61% and a high permeation flux of 2.28×10(-5)m(3)/m(2)s at operating pressure of 68kPa.

  14. Fabrication of carbon/SiO2 composites from the hydrothermal carbonization process of polysaccharide and their adsorption performance.

    Science.gov (United States)

    Li, Yinhui; Li, Kunyu; Su, Min; Ren, Yanmei; Li, Ying; Chen, Jianxin; Li, Liang

    2016-11-20

    In this work, carbon/SiO2 composites, using amylose and tetraethyl orthosilicate (TEOS) as raw materials, were successfully prepared by a facial hydrothermal carbonization process. The carbon/SiO2 composites were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), Energy Dispersive Spectroscopy (EDS), transmission electron microscope (TEM), N2 adsorption and Thermogravimetric (TG) analysis. The composites, which were made up of amorphous SiO2 and amorphous carbon, were found to have hierarchical porous structures. The mass ratios of amylose and SiO2 and the hydrothermal carbonization time had significant effects on the morphology of the composites, which had three shapes including monodispersed spheres, porous pieces and the nano-fibers combined with nano-spheres structures. The adsorption performance of the composites was studied using Pb(2+) as simulated contaminants from water. When the mass ratio of amylose and SiO2 was 9/1, the hydrothermal time was 30h and the hydrothermal temperature was 180°C, the adsorption capacity of the composites achieved to 52mg/g. Experimental data show that adsorption kinetics of the carbon/SiO2 composites can be fitted well by the Elovich model, while the isothermal data can be perfectly described by the Langmuir adsorption model and Freundlich adsorption model. The maximum adsorption capacity of the carbon/SiO2 composites is 56.18mgg(-1).

  15. He, Ne and Ar isotope compositions of fluid inclusions in hy-drothermal sulfides from the TAG hydrothermal field, Mid-Atlantic Ridge

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Helium, neon and argon isotope compositions of fluid inclusionshave been measured in hydrothermal sulfide samples from the TAG hydrothermal field at the Mid-Atlantic Ridge. Fluid-inclusion 3He/4He ratios are 2.2-13.3 times the air value (Ra), and with a mean of 7.2 Ra. Com-parison with the local vent fluids (3He/4He=7.5-8.2 Ra) and mid-ocean ridge basalt values (3He/4He=6-11 Ra) shows that the variation range of 3He/4He ratios from sulfide-hosted fluid inclu-sions is significantly large. Values for 20Ne/22Ne are from 10.2 to 11.4, which are significantly higher than the atmospheric ratio (9.8). And fluid-inclusion 40Ar/36Ar ratios range from 287 to 359, which are close to the atmospheric values (295.5). These results indicate that the noble gases of fluid inclu-sions in hydrothermal sulfides are a mixture of mantle- and seawater-derived noble gases; the partial mantle-derived components of trapped hydrothermal fluids may be from the lower mantle; the helium of fluid inclusions is mainly from upper mantle; and the Ne and Ar components are mainly from seawater.

  16. A facile approach to the elucidation of magnetic parameters of CuFe2O4 nanoparticles synthesized by hydrothermal route

    Science.gov (United States)

    Kurian, Jessyamma; Jacob Mathew, M.

    2017-04-01

    Pure pseudo cubic shaped copper ferrite nanoparticles with narrow size distribution in the range 6-17 nanometer are prepared by hydrothermal method under various synthesis conditions namely, hydrothermal temperature, heating time, and pH. The structural and morphological studies are carried out in detail using XRD and TEM analysis. The crystallite size and particle size are calculated from different characterization techniques. The distribution of cations among the tetrahedral and octahedral sites is determined from the XRD intensity calculation. Compositional features are determined from EDS analysis. Magnetic studies are carried out using VSM at room temperature and the important magnetic parameters are extracted from it. Contributions due to various types of magnetization to the total magnetization are determined from the theoretical fitting of the magnetization curve. Excellent fits are obtained for all samples prepared under various conditions. The ferromagnetic, superparamagnetic and paramagnetic contributions to the magnetization are determined from the analysis of fitted M-H curve. It is observed that the hydrothermal reaction time and temperature has little effect on the structural and magnetic parameters of the material. However, pH plays a crucial role in the physical properties of nanoparticles. Optimized synthesis conditions are identified for changing the soft ferrimagnetic nature of copper ferrite nanoparticles to superparamagnetic nature.

  17. Morphology of hydrothermally synthesized ZnO nanoparticles tethered to carbon nanotubes affects electrocatalytic activity for H2O2 detection

    Science.gov (United States)

    Wayu, Mulugeta B.; Spidle, Ryan T.; Devkota, Tuphan; Deb, Anup K.; Delong, Robert K.; Ghosh, Kartik C.; Wanekaya, Adam K.; Chusuei, Charles C.

    2013-01-01

    We describe the synthesis of zinc oxide (ZnO) nanoparticles and demonstrate their attachment to multiwalled carbon tubes, resulting in a composite with a unique synergistic effect. Morphology and size of ZnO nanostructures were controlled using hydrothermal synthesis, varying the hydrothermal treatment temperature, prior to attachment to carboxylic acid functionalized multi-walled carbon nanotubes for sensing applications. A strong dependence of electrocatalytic activity on nanosized ZnO shape was shown. High activity for H2O2 reduction was achieved when nanocomposite precursors with a roughly semi-spherical morphology (no needle-like particles present) formed at 90 °C. A 2.4-fold increase in cyclic voltammetry current accompanied by decrease in overpotential from the composites made from the nanosized, needle-like-free ZnO shapes was observed as compared to those composites produced from needle-like shaped ZnO. Electrocatalytic activity varied with pH, maximizing at pH 7.4. A stable, linear response for H2O2 concentrations was observed in the 1–20 mM concentration range. PMID:25684785

  18. Polarization reversal in BaTiO{sub 3} nanostructures synthesized by microwave-assisted hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Velasco-Davalos, Ivan; Ambriz-Vargas, Fabian [Centre Énergie, Matériaux et Télécommunications, INRS, 1650 Lionel-Boulet, Varennes, Québec J3X1S2 (Canada); Gómez-Yáñez, Carlos [Departamento de Ingeniería en Metalurgia y Materiales, ESIQIE, Instituto Politécnico Nacional, UPALM, Zacatenco, CP 07738 DF, México (Mexico); Thomas, Reji, E-mail: reji.thomas@emt.inrs.ca [Centre Énergie, Matériaux et Télécommunications, INRS, 1650 Lionel-Boulet, Varennes, Québec J3X1S2 (Canada); Ruediger, Andreas, E-mail: ruediger@emt.inrs.ca [Centre Énergie, Matériaux et Télécommunications, INRS, 1650 Lionel-Boulet, Varennes, Québec J3X1S2 (Canada)

    2016-05-15

    Ferroelectric BaTiO{sub 3} nanostructures and thin films were deposited by a microwave assisted hydrothermal process at low temperatures (<250 °C) on metallic Pt/Al{sub 2}O{sub 3}/SiO{sub 2}/Si and Nb:SrTiO{sub 3} (100) substrates. TiO{sub 2} nanoparticles dispersed in the Ba(OH){sub 2} alkaline solution are used as the precursors without any mineralizers. The incorporation of H{sub 2}O{sub 2} into precursor solution served as a strong oxidant and catalyst for the uniform nucleation of BaTiO{sub 3} on the substrate surface. The polycrystalline and epitaxial nature of the films were confirmed by atomic force microscopy and x-ray diffraction studies. We report the ferroelectric behavior of BaTiO{sub 3} films on Nb:SrTiO{sub 3} (100) substrates by piezoresponse force microscopy. - Highlights: • Microwave assisted hydrothermal deposition of highly ordered BaTiO{sub 3} thin films on single crystal substrates. • Fast growth without the needof any mineralizers. • Moderate addition of H{sub 2}O{sub 2} significantly improves the surface coverage. • H{sub 2}O{sub 2} substantially reduces hydrogen incorporation into the film and the associated leakage current. • Out-of-plane polarization reversal demonstrated locally.

  19. He, Ne and Ar isotope compositions of fluid inclusions in hy-drothermal sulfides from the TAG hydrothermal field, Mid-Atlantic Ridge

    Institute of Scientific and Technical Information of China (English)

    ZENG; Zhigang; (

    2001-01-01

    [1]Rona, P. A. , Klinkhammer, G. , Nelsen, T. A. et al. , Black smokers, massive sulphides and vent biota at the Mid-Atlantic Ridge, Nature, 1986, 321: 33.[2]Edmonds, H. N. , German, C. R. , Green, D. R. H. et al. , Continuation of the hydrothermal fluid chemistry time series at TAG, and the effects of ODP drilling, Geophys. Res. Lett., 1996, 23: 3487.[3]Charlou, J. L. , Donval, J. P. , Jean-Baptiste, P. et al. , Gases and helium isotopes in high temperature solutions sampled before and after ODP Leg158 drilling at TAG hydrothermal field (26°N, MAR), Geophys. Res. Lett., 1996, 23: 3491. [4]Rudnicki, M. D. , Elderfield, H. , Helium, radon and manganese at the TAG and Snakepit hydrothermal vent fields, 26°and 23°N, Mid-Atlantic Ridge, Earth Planet. Sci. Lett., 1992, 113: 307. [5]Butterfield, D. A. , Massoth, G. J. , McDuff, R. E. et al. , Geochemistry of fluids from Axial Seamount hydrothermal emissions study vent field, Juan de Fuca Ridge: Subseafloor boiling and subsequent fluid-rock interaction, Journal of Geophysical Research, 1990, 95: 12895. [6]Baker, E. T. , Lupton, J. E. , Changes in submarine hydrothermal 3He/heat ratios as an indicator of magmatic/tectonic activity, Nature, 1990, 346: 556. [7]Jean-Baptiste, P. , Fouquet, Y. , Abundance and isotopic composition of helium in hydrothermal sulfides from the East Pacific Rise at 13°N, Geochimica et Cosmochimica Acta, 1996, 60: 87. [8]Stuart, F. M. , Turner, G. , Duckworth, R. C. et al. , Helium isotopes as tracers of trapped hydrothermal fluids in ocean-floor sulfides, Geology, 1994, 22: 823. [9]Stuart, F. M. , Duckworth, R. , Turner, G. et al. , Helium and sulfur isotopes in sulfide minerals from Middle Valley, Northern Juan de Fuca Ridge, Proceedings of the Ocean Drilling Program, Scientific Results, 1994, 139: 387. [10]Turner, G. , Stuart, F. , Helium/heat ratios and deposition temperatures of sulphides from the ocean floor, Nature, 1992, 357: 581.[11

  20. Thermal degradation of 2,2',4,4'-tetrabromodiphenyl ether (BDE-47) over synthesized Fe-Al composite oxide.

    Science.gov (United States)

    Yang, Fan; Li, Qianqian; Su, Guijin; Huang, Xinchen; Li, Binke; Zhao, Yanhui; Miao, Xue; Zheng, Minghui

    2016-05-01

    A series of Fe-Al composite oxides were synthesized by the hydrothermal method using different urea dosages and examined towards the degradation of 2,2',4,4'-tetrabromodiphenyl ether (BDE-47) at 300 °C. The as-prepared oxides were characterized by field-emission scanning electron microscopy, X-ray diffraction and energy-dispersive X-ray spectroscopy. The morphology and composition of the prepared materials could be regulated by controlling the urea concentration. Interestingly, these properties influenced the nature and amount of the hydrodebromination products generated during the degradation of BDE-47. The degradation of BDE-47 over the composite oxide prepared at a urea dosage of 3 mmol generated BDE-17 as the major isomer product, followed by BDE-28/33, -30, and -32, among the tribromodiphenyl ethers (tri-BDEs). Regarding the dibromodiphenyl ethers (di-BDEs) produced, the amount of the isomers decreased in the order of BDE-8/11 > BDE-7 > BDE-15 > BDE-10. And the BDE-1 among monobromodiphenyl was determined. In contrast, over the composite oxides prepared at urea dosages greater than 3 mmol, BDE-28/33 gradually become the major isomer product instead of BDE-17 among tri-BDEs. The amount of the other di-BDEs isomer such as BDE-15 and -10 approach to be comparable to that BDE-8/11. However, regardless of the urea dosage, BDE-47 converted into BDE-75 via an isomerization reaction. Based on these intermediate products identification, a possible hydrodebromination mechanism of BDE-47 over Fe-Al composite oxide was comprehensively traced. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Enhancement of zinc vacancies in room-temperature ferromagnetic Cr–Mn codoped ZnO nanorods synthesized by hydrothermal method under high pulsed magnetic field

    Energy Technology Data Exchange (ETDEWEB)

    Zhong, Min [Laboratory for Microstructures/School of Materials Science and Engineering, Shanghai University, 149 Yanchang Road, 200072 Shanghai (China); Li, Ying, E-mail: liying62@shu.edu.cn [Laboratory for Microstructures/School of Materials Science and Engineering, Shanghai University, 149 Yanchang Road, 200072 Shanghai (China); Hu, Yemin; Zhu, Mingyuan; Li, Wenxian; Jin, Hongmin; Wang, Shiwei [Laboratory for Microstructures/School of Materials Science and Engineering, Shanghai University, 149 Yanchang Road, 200072 Shanghai (China); Li, Yibing; Zhao, Huijun [Centre for Clean Environment and Energy, Griffith School of Environment, Griffith University, Gold Coast Campus, QLD 4222 (Australia)

    2015-10-25

    Room-temperature ferromagnetic Cr–Mn codoped ZnO diluted magnetic semiconductor was synthesized by pulse magnetic field-assisted hydrothermal method. X-ray diffraction and Raman spectra analysis reveal that all the samples have hexagonal wurtzite structure. High resolution transmission electron microscopy and Energy-dispersive spectroscopy measurements ensure that the Cr and Mn ions are incorporated into the wurtzite host matrix without any detectable impurity phase. X-ray photoelectron spectroscopy confirms that Mn and Cr ions are doped into the ZnO wurtzite host matrix with divalent states in the sample without magnetic field processing. Cr ions became trivalent states in ZnO synthesized with high pulsed magnetic field, while Mn keeps its divalent state. The presence of Cr{sup 3+} is attributed to hole doping in ZnO with zinc vacancies induced by the field. Magnetization measurements reveal the appearance of ferromagnetism for the magnetic field processed sample. Comparing with oxygen vacancies, zinc vacancies (hole doping) is more effectively to stabilized ferromagnetism in Mn-doped ZnO diluted magnetic semiconductors. - Graphical abstract: This figure shows the magnetization versus magnetic field curves for ZnO–Cr–Mn-0T and ZnO–Cr–Mn-4T at 290 K. The 4 T sample was well-defined hysteresis loops, which is indicative of room-temperature ferromagnetic behavior. But for 0 T sample, no ferromagnetic response at 290 K is observed. The hole doping enhanced by high pulsed magnetic field is crucial to stabilize ferromagnetism in Mn-doped ZnO diluted magnetic semiconductor. And the presence of Cr{sup 3+} in 4 T sample is a possible signature of hole doping induced by zinc vacancies. - Highlights: • Cr–Mn codoped ZnO nanorods were synthesized by hydrothermal method. • High pulsed magnetic field was applied during the hydrothermal method. • The valence state of doped elements was investigated by XPS. • High pulsed magnetic field enhances the

  2. Magnetic Properties of Co0.5Zn0.5Fe2O4 Nanoparticles Synthesized by a Template-Assisted Hydrothermal Method

    Directory of Open Access Journals (Sweden)

    H. Y. He

    2011-01-01

    Full Text Available In the present paper, nickel cobalt ferrite (Co0.5Zn0.5Fe2O4 nanoparticles were synthesized using a template-assisted hydrothermal method. Carboxymethyl cellulose was used as the templating agent for controlling the morphology of the Co0.5Zn0.5Fe2O4 nanoparticles. The synthesized nanoparticles were characterized using X-ray diffraction, scanning electron microscopy, and a vibrating sample magnetometer. The results indicated that the morphology of the nanoparticles changed from granular and superparamagnetic to platelike and ferromagnetic with the addition of the template. The Co0.5Zn0.5Fe2O4 nanoparticles synthesized without the template exhibited a saturation magnetization and coercivity 2.81 T and 0.2 kA⋅m−1, while when the template was used, the saturation magnetization and coercivity increased to 3.13 T and 76.6 kA⋅m−1 as the template proportion increased to 0.3.

  3. Composition of proteins in okara as a byproduct in hydrothermal processing of soy milk.

    Science.gov (United States)

    Stanojevic, Sladjana P; Barac, Miroljub B; Pesic, Mirjana B; Vucelic-Radovic, Biljana V

    2012-09-12

    Protein quality, based on its subunit composition, in okara obtained as a byproduct during hydrothermal cooking of soy milk was assessed. The composition of 7S and 11S protein fractions was correlated with the physicochemical properties of protein in okara produced from six soybean varieties. The basic 7S globulin (Bg7S) and 11S protein were two main proteins in okara. Investigated soybean genotypes produced okara with mainly acidic A(5) and basic B(1,2,4) polypeptides of 11S proteins. Soybean 11S content was not an indicator of okara protein recovery or extractability. Of all tested relationships, extractable soluble protein content of okara was influenced only by soybean Bg7S (r = 0.86; p soybeans (r = 0.81; p functional ingredient.

  4. Hydrothermal synthesis of TiO2/WO3 compositions and their photocatalytic activity

    Science.gov (United States)

    Pyachin, Sergey A.; Karpovich, Natalia F.; Zaitsev, Alexey V.; Makarevich, Konstantin S.; Burkov, Alexander A.; Ustinov, Alexander Yu.

    2016-11-01

    Photocatalytic activity, optical properties, thermal stability, phase patterns and morphology of nano-size TiO2/WO3 compositions obtained from organic precursors through hydrothermal synthesis have been studied. It has been shown that doping of anatase nanoparticles with tungsten W+6 results in particle diameter reduction from 35 to 10 nm; decrease in width of the band gap from 3.15 eV to 2.91 eV and increase in temperature of phase transition of anatase to rutile up to 980oC. Catalytic activity of TiO2/WO3 (4 mol.%) composition under photochemical methylene blue (MB) oxidation by simulated solar light exceeds that of undoped anatase (obtained in the same way) 6-fold.

  5. Lithium manganese oxide (LiMn2O4) nanoparticles synthesized by hydrothermal method as adsorbent of lithium recovery process from geothermal fluid of Lumpur Sidoarjo

    Science.gov (United States)

    Noerochim, Lukman; Sapputra, Gede Panca Ady; Widodo, Amien

    2016-04-01

    Lumpur Sidoarjo is one of geothermal fluid types which has a great potential as source of lithium. Adsorption method with Lithium Manganese Oxide (LiMn2O4) as an adsorbent has been chosen for lithium recovery process due to low production cost and environmental friendly. LiMn2O4 was synthesized by hydrothermal method at 200 °C for 24 hrs, 48 hrs, and 72 hrs. As prepared LiMn2O4 powder is treated by acid treatment with 0.5 M HCl solution for 24 hrs. XRD test result reveals that all of as-prepared samples are indexed as spinel structure of LiMn2O4 (JCPDS card no 35-0782) with no impurity peaks detected. SEM images show that LiMn2O4 has nanoparticles morphology with particle size around 25 nm. The highest adsorption efficiency of adsorbent is obtained by sample hydrothermal for 72 hrs with 42.76%.

  6. Magnetic Properties for the Single-domain CoFe2O4 Nano-particles Synthesized by the Hydrothermal Method

    Institute of Scientific and Technical Information of China (English)

    YANG Zhi; ZHANG Yue; SONG Yu; WANG Jiawei; CHEN Yuang; ZHANG Zhe; DUAN Nian; RUAN Xuefeng

    2015-01-01

    The aim of this work was to investigate the size-related magnetism for the single-domain CoFe2O4 nano-particles synthesized using the hydrothermal method. The effects of the reaction temperature and the reaction time on the lattice constants, particle morphologies, and the room-temperature magnetic properties were studied from the X-ray diffraction, the transmission electron microscope, and the vibrating-sample magnetometer. The experimental results show that the samples are composed of CoFe2O4 nano-particles with an average crystallite size (D) smaller than 40 nm, and the magnetic properties of the samples can be manipulated in a wide range:the MS values vary from smaller than 50 emu/g to close to 80 emu/g, and the HC values are between about 200 Oe and 2000 Oe. Additionally, the relationship between HC and 1/D3/2 satisifes linearship, showing the characteristic of single-domain structure. These results indicate that the single-domain CoFe2O4 nano-particles with size controlled between the superparamagnetic critical size and single-domain critical size can be easily prepared using this hydrothermal method.

  7. A Simple and Efficient Method for Synthesizing Te Nanowires from CdTe Nanoparticles with EDTA as Shape Controller under Hydrothermal Condition

    Directory of Open Access Journals (Sweden)

    Fangfang Xue

    2012-01-01

    Full Text Available We developed a simple and efficient method for synthesizing Te nanowires from CdTe nanoparticles with ethylenediaminetetraacetic acid disodium salt dehydrate (EDTA as shape controller under hydrothermal condition. The system could both complete the transformation to Te and reduce the interference of CdTeS by adjusting the concentration of EDTA, which was proved by inductively coupled plasma mass spectrometry, X-ray diffraction patterns, and Raman spectra. It was found that the as-prepared Te nanowires display strong fluorescence emission in the blue-violet region. The nanowires exhibit a pretty good morphology with the average diameter of ca. 30 nm and a length up to micrometer scale. Moreover, a possible transformation mechanism of CdTe nanoparticles into Te nanowires is also discussed.

  8. The Effect of Sodium Dodecyl Sulfate (SDS and Cetyltrimethylammonium Bromide (CTAB on the Properties of ZnO Synthesized by Hydrothermal Method

    Directory of Open Access Journals (Sweden)

    Yun Hin Taufiq-Yap

    2012-10-01

    Full Text Available ZnO nanostructures were synthesized by hydrothermal method using different molar ratios of cetyltrimethylammonium bromide (CTAB and Sodium dodecyl sulfate (SDS as structure directing agents. The effect of surfactants on the morphology of the ZnO crystals was investigated by field emission scanning electron microscopy (FESEM and transmission electron microscopy (TEM techniques. The results indicate that the mixture of cationic-anionic surfactants can significantly modify the shape and size of ZnO particles. Various structures such as flakes, sheets, rods, spheres, flowers and triangular-like particles sized from micro to nano were obtained. In order to examine the possible changes in other properties of ZnO, characterizations like powder X-ray diffraction (PXRD, thermogravimetric and differential thermogravimetric analysis (TGA-DTG, FTIR, surface area and porosity and UV-visible spectroscopy analysis were also studied and discussed.

  9. Photocatalytic Degradation of Municipal Wastewater and Brilliant Blue Dye Using Hydrothermally Synthesized Surface-Modified Silver-Doped ZnO Designer Particles

    Directory of Open Access Journals (Sweden)

    Tabasom Parvin

    2012-01-01

    Full Text Available Photocatalytic degradation of local municipal wastewater and brilliant blue FCF dye were investigated using silver-doped ZnO designer particles. The silver-doped ZnO designer particles were synthesized under mild hydrothermal conditions (T = 150–250∘C, =autogeneous, experimental duration = 16–24 h in the presence of surface modifiers. The resultant products were characterized using powder XRD, FTIR, Zeta potential, and SEM. Various parameters including catalyst amount, light source, pH, and photocatalytic time duration were studied to find out their effects on photodegradation efficiency with respect to municipal wastewater and brilliant blue dye. The effect of these parameters was evaluated using chemical oxygen demand (COD and % transmittance analyses. The photodegradation results showed that the surface-modified silver-doped ZnO designer particles had higher efficiency compared to the reagent-grade ZnO in photodegradation of municipal wastewater and brilliant blue dye.

  10. Hydrothermal syntheses and structural characterizations of three polyoxomolybdates frameworks linked by M(HL)2 units(M=Co,Ni,Zn;L=3-(2-pyridyl)pyrazole)

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Three polyoxomolybdate compounds,namely {[MII(HL)2]2(Mo8O26)}n(M = Co(1),Ni(2),Zn(3))(HL,3-(2-pyridyl)pyrazole),were designed and synthesized under the hydrothermal conditions and characterized by elemental analysis,IR spectroscopy,and TGA.Single-crystal X-ray diffraction analysis results reveal that compounds 1-3 own the isostructural chain structure consisting of the β-[Mo8O26]4- anions,which are linked by M(HL)22+ units via the terminal oxygen atoms.TGA curves show that the organic ligands separate from the related compounds above ca.673 K.

  11. Gas sensing properties of graphene–WO{sub 3} composites prepared by hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Chu, Xiangfeng, E-mail: xfchu99@ahut.edu.cn [School of Chemistry and Chemical Engineering, Anhui University of Technology, Maanshan 243002 (China); Hu, Tao [School of Chemistry and Chemical Engineering, Anhui University of Technology, Maanshan 243002 (China); Gao, Feng [Department of Materials Science and Engineering, Nanjing University, Nanjing 210093 (China); Dong, Yongping; Sun, Wenqi; Bai, Linshan [School of Chemistry and Chemical Engineering, Anhui University of Technology, Maanshan 243002 (China)

    2015-03-15

    Graphical abstract: - Highlights: • The amount of graphene had an effect on the morphology of graphene–WO{sub 3} composites. • The optimum temperature of 0.1 wt% graphene–WO{sub 3} sensor to acetaldehyde was 100 °C. • 0.1 wt% graphene–WO{sub 3} sensor exhibited good selectivity to acetaldehyde at 100 °C. - Abstract: Graphene–WO{sub 3} composites mixed with different amounts of graphene (0, 0.1, 0.5, 1 and 3 wt%) were prepared by hydrothermal method at 180 °C for 24 h. The as-prepared graphite oxide, graphene and graphene–WO{sub 3} composites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectra (FT-IR) and Raman spectroscopy, respectively. The effect of the amount of graphene in the composites on the gas-sensing responses and the gas-sensing selectivity of the materials was investigated. The experimental results revealed that the sensor based on 0.1 wt% graphene–WO{sub 3} composite exhibited high response and good selectivity to acetaldehyde vapor at 100 °C, the optimum operating temperature of this sensor to 1000 ppm acetaldehyde vapor decreased from 180 °C to 100 °C comparing with that of pure WO{sub 3}. The response time and the recovery time for 100 ppm acetaldehyde vapor were 250 s and 225 s, respectively.

  12. Potentiometric study of polyaniline film synthesized with various dopants and composite-dopant: A comparative study

    Indian Academy of Sciences (India)

    P D Gaikwad; D J Shirale; V K Gade; P A Savale; K P Kakde; H J Kharat; M D Shirsat

    2006-08-01

    The potentiometric study of polyaniline (PANI) film synthesized with dopants viz. polyvinyl sulfonic acid (PVS), -toluene sulfonic acid (TS), dodecyl benzene sulfonic acid (DBS) and composite-dopants viz. PVS–TS and PVS–DBS, has been carried out. The synthesized PANI films were characterized by electrochemical technique, UV-visible spectroscopy, Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM) and conductivity measurement. It was found that the PANI doped with PVS gives good electrochemical properties, conductivity as well as surface morphology as compared to TS and DBS, whereas in composite dopants the PANI doped with PVS–TS gives good polymer matrix as compared to PVS–DBS.

  13. Sonochemically synthesized iron-doped zinc oxide nanoparticles: Influence of precursor composition on characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Roy, Anirban [Department of Chemical Engineering, University of Calcutta, 92, Acharya P. C. Road, Kolkata 700 009 (India); Maitra, Saikat [Government College of Engineering and Ceramic Technology, 73, A.C. Banerjee Lane, Kolkata 700 010 (India); Ghosh, Sobhan [Managing Innovations, House No. 188, Sector 14, Faridabad 121 007 (India); Chakrabarti, Sampa, E-mail: scchemengg@caluniv.ac.in [Department of Chemical Engineering, University of Calcutta, 92, Acharya P. C. Road, Kolkata 700 009 (India); Centre for Research in Nanoscience & Nanotechnology, University of Calcutta JD- 2, Sector-III, Salt Lake, Kolkata 700 098 (India)

    2016-02-15

    Highlights: • Sonochemical synthesis of iron-doped zinc oxide nanoparticles. • Green synthesis without alkali at room temperature. • Characterization by UV–vis spectroscopy, FESEM, XRD and EDX. • Influence of precursor composition on characteristics. • Composition and characteristics are correlated. - Abstract: Iron-doped zinc oxide nanoparticles have been synthesized sonochemically from aqueous acetyl acetonate precursors of different proportions. Synthesized nanoparticles were characterized with UV–vis spectroscopy, X-ray diffraction and microscopy. Influences of precursor mixture on the characteristics have been examined and modeled. Linear correlations have been proposed between dopant dosing, extent of doping and band gap energy. Experimental data corroborated with the proposed models.

  14. Photocatalytic hydrogen generation over porous ZnIn{sub 2}S{sub 4} microspheres synthesized via a CPBr-assisted hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Bai, Xuefeng, E-mail: bxuefeng@163.net [Institute of Petrochemistry, Heilongjiang Academy of Sciences, Harbin 150040 (China); School of Chemistry and Materials, Heilongjiang University, Harbin 150070 (China); Li, Jinshu [School of Chemistry and Materials, Heilongjiang University, Harbin 150070 (China)

    2011-07-15

    Graphical abstract: ZnIn{sub 2}S{sub 4} porous microspheres were synthesized via a cetylpyridinium bromide (CPBr)-assisted hydrothermal method. It could be seen from the SEM image that the flowerlike microspheres were composed of numerous nanosheets. Many slit-like pores were formed among the curved nanosheets. The porous structure benefited the adsorption of reactants, the diffuseness of products, the charge separation on surface, the transfer of the interfacial charge carriers and the charge carrier trapping. And porous ZnIn{sub 2}S{sub 4} photocatalyst exhibited higher photocatalytic activity than nonporous ZnIn{sub 2}S{sub 4} material. Highlights: {yields} A series of unique flower-like porous ZnIn{sub 2}S{sub 4} microspheres of hexagonal crystal phase as efficient visible-light photocatalysts have been synthesized through CPBr-assisted hydrothermal method. {yields} The CPBr addition would visibly influence the self-assemble growing and the crystal structure including the position and intensity of some peaks. {yields} We also found that the pH value plays a crucial role in the formation of ZnIn{sub 2}S{sub 4} porous microspheres and the influence of the pH on the structure of product has been first reported in our paper. {yields} The results showed that our as-synthesized porous ZnIn{sub 2}S{sub 4} microspheres possessed a specific surface area of 165.4 m{sup 2} g{sup -1} and performed higher visible-light photocatalytic activity than bulk ZnIn{sub 2}S{sub 4} for hydrogen evolution. The maximum H{sub 2} evolution rate of ZnIn{sub 2}S{sub 4} reaches 1544.8 {mu}mol/(h g). -- Abstract: Hexagonal ZnIn{sub 2}S{sub 4} porous microspheres were synthesized via a cetylpyridinium bromide (CPBr)-assisted hydrothermal method. The structure, morphology and optical property of these prepared products were characterized by wide angle X-ray diffraction (WAXRD), small angle X-ray diffraction (SAXRD), UV-Vis diffusive reflectance spectroscopy (DRS), field emission scanning

  15. The effect of Cu doping on the mechanical and optical properties of zinc oxide nanowires synthesized by hydrothermal route

    Science.gov (United States)

    Robak, Elżbieta; Coy, Emerson; Kotkowiak, Michał; Jurga, Stefan; Załęski, Karol; Drozdowski, Henryk

    2016-04-01

    Zinc oxide (ZnO) is a wide-bandgap semiconductor material with applications in a variety of fields such as electronics, optoelectronic and solar cells. However, much of these applications demand a reproducible, reliable and controllable synthesis method that takes special care of their functional properties. In this work ZnO and Cu-doped ZnO nanowires are obtained by an optimized hydrothermal method, following the promising results which ZnO nanostructures have shown in the past few years. The morphology of as-prepared and copper-doped ZnO nanostructures is investigated by means of scanning electron microscopy and high resolution transmission electron microscopy. X-ray diffraction is used to study the impact of doping on the crystalline structure of the wires. Furthermore, the mechanical properties (nanoindentation) and the functional properties (absorption and photoluminescence measurements) of ZnO nanostructures are examined in order to assess their applicability in photovoltaics, piezoelectric and hybrids nanodevices. This work shows a strong correlation between growing conditions, morphology, doping and mechanical as well as optical properties of ZnO nanowires.

  16. Alkaline hydrothermal zeolites synthesized from high SiO{sub 2} and Al{sub 2}O{sub 3} co-disposal fly ash filtrates

    Energy Technology Data Exchange (ETDEWEB)

    Vernon S. Somerset; Leslie F. Petrik; Richard A. White; Michael J. Klink; David Key; Emmanuel I. Iwuoha

    2005-12-01

    A co-disposal reaction was used wherein fly ash (FA) was reacted with acid mine drainage (AMD), to collect filtrates for zeolite synthesis. Raw fly ash as well as fly ash leached with HCl were subjected to the same alkaline hydrothermal zeolite synthesis conditions, as for the co-disposal filtrates, in order to evaluate the zeolitic material obtained. The Si and Al contents of the fly ash (FA) filtrates were used as precursor species for the alkaline hydrothermal conversion of the fly ash filtrates into zeolites. These filtrates were then analysed by XRF spectrometry for quantitative determination of SiO{sub 2} and Al{sub 2}O{sub 3}. The (SiO{sub 2})/(Al{sub 2}O{sub 3}) ratio obtained in the filtrates range from 1.4 to 2.5. The (SiO{sub 2})/(Al{sub 2}O{sub 3}) ratio was used to predict whether the fly ash filtrates could successfully be converted into faujasite zeolitic material by the adopted synthesis procedures. If the (SiO{sub 2})/(Al{sub 2}O{sub 3}) ratio is higher than 1.5 in the co-disposal filtrates, it favours the formation of faujasite. The zeolite synthesis included an alkaline fusion of the co-disposal filtrates, followed by aging for 8 hours and hydrothermal conversion by crystallisation at 100{sup o}C. Different variables were investigated during the synthesis of zeolite to ascertain their influence on the end product. These variables include adding different amounts of deionised water to the FA-related starting material, using different compositions of FA related starting material and different FA:NaOH ratios in fusing the starting material. 15 refs., 3 figs., 2 tabs.

  17. Hydrothermal synthesis of MoO{sub 3} nanobelt-graphene composites

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Xiaofei; Ding, Heyi; Zhang, Du; Yan, Xuehua; Lu, Chunyu; Qin, Jieling; Tang, Hua; Song, Haojie [School of Materials Science and Engineering, Jiangsu University, Zhenjiang 212013 (China); Zhang, Rongxian [School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China)

    2011-11-15

    A composite of graphene sheets decorated with molybdenum trioxide (MoO{sub 3}) nanobelts has been fabricated via a facile and efficient hydrothermal route in the presence of NaCl. The structure, morphology of these promising composites were investigated by means of field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy and thermogravimetric (TG) analysis. FESEM and TEM studies suggest the presence of uniform crystalline MoO{sub 3} nanobelts and graphene sheets in as-prepared hybrid materials. XRD and Raman results confirm the reduction of graphite oxide (GO) sheets to graphene sheets accompanying by the formation of MoO{sub 3} nanobelts. Moreover, thermal properties of GO and MoO{sub 3} nanobelt-graphene composites reveal that thermal stability of the obtained MoO{sub 3} nanobelt-graphene composites is obviously higher than that of GO due to the transformation of GO sheets to highly stable graphene sheets in the hybrids. This work could provide new insights into the fabrication of high quality MoO{sub 3}-graphene hybrid nanomaterials and facilitate their potential applications in different fields. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  18. Hollow Carbon Microspheres/MnO2 Nanosheets Composites:Hydrothermal Synthesis and Electrochemical Behaviors

    Institute of Scientific and Technical Information of China (English)

    Hui-li Fan; Fen Ran; Xuan-xuan Zhang; Hai-ming Song; Xiao-qin Niu; Ling-bin Kong; Long Kang

    2015-01-01

    This article reported the electrochemical behaviors of a novel hollow carbon microspheres/manganese dioxide nanosheets (micro-HC/nano-MnO2) composite prepared by an in situ self-limiting deposition method under hydrothermal condition. The results of scanning electron microscopy reveal that MnO2 nanosheets homogeneously grow onto the surface of micro-HC to form a loose-packed microstructure. The quantity of MnO2 required in the electrode layer has thereby been reduced significantly, and higher specific capacitances have been achieved. The micro-HC/nano-MnO2 electrode presents a high capacitance of 239.0 F g-1 at a current density of 5 mA cm-2, which is a strong promise for high-rate electro-chemical capacitive energy storage applications.

  19. The bulk isotopic composition of hydrocarbons in subaerial volcanic-hydrothermal emissions from different tectonic settings

    Science.gov (United States)

    Fiebig, J.; Tassi, F.; Vaselli, O.; Viveiros, M. F.; Silva, C.; Lopez, T. M.; D'Alessandro, W.; Stefansson, A.

    2015-12-01

    Assuming that methane and its higher chain homologues derive from a common source, carbon isotope patterns have been applied as a criterion to identify occurrences of abiogenic hydrocarbons. Based on these, it has been postulated that abiogenic hydrocarbon production occurs within several (ultra)mafic environments. More evolved volcanic-hydrothermal systems may also provide all the prerequisites necessary for abiogenic hydrocarbon production, such as availability of inorganic CO2, hydrogen and heat. We have investigated the chemical and isotopic composition of n-alkanes contained within subaerial hydrothermal discharges emitted from a range of hot spot, subduction and rift-related volcanoes to determine the origin of hydrocarbons in these systems. Amongst these are Nisyros (Greece), Vesuvio, Campi Flegrei, Ischia, Pantelleria and Vulcano (all Italy), Mt. Mageik and Trident (USA), Copahue (Argentina), Teide (Spain), Furnas and Fogo (Portugal). The carbon isotopic composition of methane emitted from these sites varies from -65 to -8‰ , whereas δ13C of ethane and propane exhibit a much narrower variation from -17‰ to -31‰. Methane that occurs most enriched in 13C is also characterized by relatively positive δD values ranging up to -80‰. Carbon isotope reversals between methane and ethane are only observed for locations exhibiting δ13C-CH4 values > -20‰, such as Teide, Pantelleria, Trident and Furnas. At Furnas, δ13C-CH4 varies by 50‰ within a relatively short distance of <50m between two vents, whereas δ13C-C2H6 varies by less than 2‰ only. For some of the investigated locations apparent carbon isotopic temperatures between methane and CO2 are in agreement with those derived from gas concentration geothermometers. At these locations methane, however seems to be in disequilibrium with ethane and propane. These findings imply that methane on the one hand and the C2+ hydrocarbons on the other hand often might derive from distinct sources.

  20. One-pot synthesis of carbon-coated SnO2 nano-composite using hydrothermal method for lithium ion battery application.

    Science.gov (United States)

    Lee, Hye Rim; Kim, Hwan Jin; Park, Jong Hyeok; Yoon, Dae Ho

    2013-06-01

    Carbon-coated SnO2 nano-composite was synthesized by using a hydrothermal method in a one step process with sizes of 1 to 3 microm. The carbon-coated SnO2 nano-composite was easily obtained by changing firing atmosphere from air to argon (600 degrees C for 3 hours). The carbon-coating thickness and size of the SnO2 nanoparticles in carbon-coated SnO2 nano-composite were confirmed through a high-resolution transmission electron microscopy (HRTEM) as 40 and 5 nm, respectively. Carbon-coating and particle size affect to the capacity retention property. Carbon-coated and non carbon-coated samples were investigated as anode materials. It was confirmed that the non carbon-coated SnO2 nano-composite had a 718 mA h/g initial charge capacity, 91% reached to theoretical value of SnO2 (790 mA h/g), while the carbon-coated SnO2 nano-composite had an excellent capacity retention of 89.6% after 70 cycles (10.88% for non carbon-coated SnO2 nano-composite).

  1. Preparation of γ-Fe2O3/Ni2O3/FeCl3(FeCl2 Composite Nanoparticles by Hydrothermal Process Useful for Ferrofluids

    Directory of Open Access Journals (Sweden)

    Qingmei Zhang

    2011-01-01

    Full Text Available Using a hydrothermal process in FeCl2 solution, γ-Fe2O3/Ni2O3/FeCl3(FeCl2 composite nanoparticles were obtained from the FeOOH/Ni(OH2 precursor prepared by coprecipitation. The precursor and the as-prepared nanoparticles were investigated by vibrating sample magnetometer (VSM, X-ray diffraction (XRD, energy disperse X-ray spectroscopy (EDX, X-ray photoelectron spectroscopy (XPS, and transmission electron microscopy (TEM. The experimental results showed that the paramagnetic amorphous precursor, in which Ni(OH2 is formed outside FeOOH, is transformed to ferrimagnetic γ-Fe2O3/Ni2O3 composite when it is processed in FeCl2 solution (0.25, 0.50, 1.00 M in an autoclave at 100°C for 1 hr. In addition, the dismutation reaction of FeCl2 produces FeCl3 and Fe. Some FeCl3 and little FeCl2 can be absorbed to form γ-Fe2O3/Ni2O3/FeCl3(FeCl2 composite nanoparticles in which Ni2O3 forms outside the γ-Fe2O3 core and the outermost layer is FeCl3 (FeCl2. The content of FeCl3 (FeCl2 in the particles increased, and the magnetization of the particles decreased with the concentration of FeCl2 solution increasing in the hydrothermal process. The FeCl3 (FeCl2 surface is chemically passive and nonmagnetic (paramagnetic. Accordingly, the composite nanoparticles are chemically stable, and their aggregation is prevented. The specific saturation magnetization of such composite nanoparticles can get to 57.4–62.2 emu/g and could be very suitable for synthesizing ferrofluids.

  2. Surface properties and dye loading behavior of Zn{sub 2}SnO{sub 4} nanoparticles hydrothermally synthesized using different mineralizers

    Energy Technology Data Exchange (ETDEWEB)

    Annamalai, Alagappan; Eo, Yang Dam [Department of Advanced Technology Fusion, Konkuk University, 1 Hwayang-dong, Kwangjin-gu, Seoul 143-701 (Korea, Republic of); Im, Chan [Department of Chemistry, Konkuk University, 1 Hwayang-dong, Kwangjin-gu, Seoul 143-701 (Korea, Republic of); Lee, Man-Jong, E-mail: leemtx@konkuk.ac.kr [Department of Advanced Technology Fusion, Konkuk University, 1 Hwayang-dong, Kwangjin-gu, Seoul 143-701 (Korea, Republic of)

    2011-10-15

    We present for the first time the influence of different mineralizers on the isoelectric point (IEP) of zinc stannate (Zn{sub 2}SnO{sub 4}) nanoparticles hydrothermally prepared using three different mineralizers, viz., Na{sub 2}CO{sub 3}, KOH and tert-butyl amine, and the effect of the IEPs on the dye loading behavior of Zn{sub 2}SnO{sub 4} based photoelectrodes in dye sensitized solar cells (DSSCs). To produce highly crystalline, uniform sized Zn{sub 2}SnO{sub 4} nanoparticles, hydrothermal processing parameters, such as reaction temperature, time, and the mineralizers used have been critically adjusted. The structural and morphological features of the as-synthesized Zn{sub 2}SnO{sub 4} nanoparticles have been observed using both scanning and transmission electron microscopy. For the surface state characterization of shape- and size-controlled Zn{sub 2}SnO{sub 4} nanoparticles, the IEPs of Zn{sub 2}SnO{sub 4} surfaces were determined through zeta potential measurements. The IEPs were found to be 5.7, 7.4 and 8.1 for Zn{sub 2}SnO{sub 4} nanoparticles formed using Na{sub 2}CO{sub 3}, KOH and tert-butyl amine, respectively, suggesting that the surface properties of Zn{sub 2}SnO{sub 4} nanoparticles can be manipulated through the choice of the mineralizers used during the hydrothermal reaction. The amount of N719 dye loading on the surfaces of Zn{sub 2}SnO{sub 4} electrodes having different IEPs was also evaluated. It was revealed that the higher the IEP, the higher the dye loading amount, which means that the IEP mainly affects the dye loading at the dye-metal oxide interface. - Highlights: {yields} The effect of various mineralizers on the isoelectric point of Zn{sub 2}SnO{sub 4} was discussed. {yields} The IEP of Zn{sub 2}SnO{sub 4} can be modified by the choice of mineralizer. {yields} Change in IEP affects the surface properties and the morphology of Zn{sub 2}SnO{sub 4} particles. {yields} Modified surface affects the N719 dye loading behaviour of the Zn{sub 2

  3. Hydrothermal Synthesis and Ammonia Sensing Properties of WO3/Fe2O3 Nanorod Composites

    Science.gov (United States)

    Dien, Nguyen Dac; Phuoc, Luong Huu; Hien, Vu Xuan; Vuong, Dang Duc; Chien, Nguyen Duc

    2017-01-01

    WO3 nanorods (NRs) and α-Fe2O3 NRs were fabricated by hydrothermal treatment. Composites of these materials were created by mixing with ratios of 1:2, 1:1 and 2:1 in weight. Morphology, structure and composition characteristics of the WO3/Fe2O3 NRs composites were characterized by scanning electron microscopy, x-ray diffraction and energy dispersive x-ray spectroscopy analyses. The results of sensing measurements indicated that the sensor based on WO3:Fe2O3 with the ratio of 2:1 exhibited fairly good sensitivity toward NH3 at 300°C and the sensor based on WO3:Fe2O3 with the ratio of 1:1 can be used as a NH3 sensor with an operating temperature of 350°C. Selectivity and response-recovery times are suitable for practical applications. Finally, the mechanism for the improvement in the gas-sensing property was discussed.

  4. Hydrothermally synthesized reduced graphene oxide/nickel hydroxide (rGO/Ni(OH)2) nanocomposite: A promising material in dye removal

    Science.gov (United States)

    Debata, Suryakanti; Das, Trupti R.; Madhuri, Rashmi; Sharma, Prashant K.

    2017-05-01

    In order to fulfill the unquenchable demand of this expanded human society, a large number of industries have grown up resulting in a severe pollution in air, soil and water as well. Industrial dye is one of the most abundant contaminant in fresh water. Here we have prepared reduced graphene oxide/nickel hydroxide nanocomposite (rGo/Ni(OH)2) by a facile hydrothermal method, aiming for the treatment of water disposed by the textile industries. The characteristic properties of the prepared sample was observed by field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR). The effect of rGo/Ni(OH)2 on the adsorption of Rhodamine B (Rh-B) in aqueous solution was investigated, mainly focusing on the removal time. It was found that, at 45 min, the composite shows a complete disappearance of the initial concentration of Rhodamine B (RhB).

  5. Hydrothermal Liquefaction Biocrude Compositions Compared to Petroleum Crude and Shale Oil

    Energy Technology Data Exchange (ETDEWEB)

    Jarvis, Jacqueline M.; Billing, Justin M.; Hallen, Richard T.; Schmidt, Andrew J.; Schaub, Tanner M.

    2017-02-17

    We provide a direct and detailed comparison of the chemical composition of petroleum crude oil (from the Gulf of Mexico), shale oil, and three biocrudes (i.e., clean pine, microalgae Chlorella sp., and sewage sludge feedstocks) generated by hydrothermal liquefaction (HTL). Ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) reveals that HTL biocrudes are compositionally more similar to shale oil than petroleum crude oil and that only a few heteroatom classes (e.g., N1, N2, N1O1, and O1) are common to organic sediment- and biomass-derived oils. All HTL biocrudes contain a diverse range of oxygen-containing compounds when compared to either petroleum crude or shale oil. Overall, petroleum crude and shale oil are compositionally dissimilar to HTL oils, and >85% of the elemental compositions identified within the positive-ion electrospray (ESI) mass spectra of the HTL biocrudes were not present in either the petroleum crude or shale oil (>43% for negative-ion ESI). Direct comparison of the heteroatom classes that are common to both organic sedimentand biomass-derived oils shows that HTL biocrudes generally contain species with both smaller core structures and a lower degree of alkylation relative to either the petroleum crude or the shale oil. Three-dimensional plots of carbon number versus molecular double bond equivalents (with observed abundance as the third dimension) for abundant molecular classes reveal the specific relationship of the composition of HTL biocrudes to petroleum and shale oils to inform the possible incorporation of these oils into refinery operations as a partial amendment to conventional petroleum feeds.

  6. Tailoring nucleation and growth conditions for narrow compositional distributions in colloidal synthesized FePt nanoparticles

    Science.gov (United States)

    Srivastava, Chandan; Nikles, David E.; Thompson, Gregory B.

    2008-11-01

    To eliminate compositional and size variabilities between individual binary nanoparticles, it is essential to control the mechanistic steps involved in nanoparticle synthesis. A common method for synthesizing FePt nanoparticles involves the simultaneous decomposition and reduction in iron and platinum precursors, respectively. This simultaneous nucleation and growth method yields wide composition and size distributions. This paper describes and experimentally validates a methodology needed to tighten composition and size distributions for this process. By engineering the surfactant chemistry with tertiary phosphines to tightly bind the iron atoms in the iron precursor, uniform platinum rich seeds form during the initial stages of the synthesis. A thermodynamically preferred heterogeneous nucleation of iron atoms into these uniform platinum seeds in the subsequent stages produces a final dispersion with uniform particle-to-particle compositions. The paper addresses the understanding for optimizing the nucleation and growth sequences for compositional control in FePt nanoparticles.

  7. Hydroxyapatite/alumina nanocrystalline composite powders synthesized by sol-gel process for biomedical applications

    Institute of Scientific and Technical Information of China (English)

    S.Khorsand; M.H.Fathi; S.Salehi; S.Amirkhanlou

    2014-01-01

    Hydroxyapatite/alumina nanocrystalline composite powders needed for various biomedical applications were successfully synthe-sized by sol-gel process. Structural and morphological investigations of the prepared composite powders were performed using X-ray dif-fractometer (XRD), scanning electron microscopy (SEM), X'Pert HighScore software, and Clemex Vision image analysis software. The re-sults show that the crystallite size of the obtained composite powders is in the range of 25 to 90 nm. SEM evaluation shows that the obtained composite powders have a porous structure, which is very useful for biomedical applications. The spherical nanoparticles in the range of 60 to 800 nm are embedded in the agglomerated clusters of the prepared composite powders.

  8. Nanocomposite YSZ-NiO Particles with Tailored Structure Synthesized in a Two-Stage Continuous Hydrothermal Flow Reactor

    DEFF Research Database (Denmark)

    Zielke, Philipp; Xu, Yu; Kiebach, Wolff-Ragnar

    2016-01-01

    the performance of energy storage and conversion devices such as fuel cells, electrolyzers and batteries is important. One promising approach to further improve these devices is the use of carefully structured nanosized materials. Nano-composite particles combining different materials in advanced geometries like......-of-the-art solid oxide fuel and electrolysis cells. The prepared particles were characterized by X-ray powder diffraction, (high resolution) transmission electron microscopy, scanning tunnel transmission microscopy and Raman spectroscopy in order to determine crystal structure, particle size, surface morphology...

  9. Fluid geochemistry of the Mondragone hydrothermal systems (southern Italy): water and gas compositions vs. geostructural setting

    Science.gov (United States)

    Cuoco, Emilio; Minissale, Angelo; Di Leo, Antonella "Magda"; Tamburrino, Stella; Iorio, Marina; Tedesco, Dario

    2017-02-01

    The geochemistry of natural thermal fluids discharging in the Mondragone Plain has been investigated. Thermal spring emergences are located along the Tyrrhenian coast in two different areas: near Padule-S. Rocco (41°7.5'N 13°53.4'E) at the foot of Mt. Petrino, and near Levagnole (41°8.5'N 13°51.3'E) at the foot of Mt. Pizzuto. The water isotopic composition of both thermal discharges is lighter than the one of local shallow groundwater (δ18O ≅ -6.3‰ SMOW vs. ≅ -5.9‰; δD ≅ -40‰ SMOW vs. ≅ -36‰, respectively) as a consequence of inland higher altitude of recharge by rainfall, suggesting that thermal water undergoes a deep and long flow-path before emerging along the coast. The chemical composition of the highest temperature samples of two areas points that fluids in the hydrothermal reservoir(s) interact with similar lithologies, since they are both hosted in the lower sedimentary carbonate formations of the Campanian-Latial Apennine succession. However, the two spring systems are different in terms of temperature and salinity (Levagnole: ≅50 °C and 8.9 g/L vs. Padule: ≅32 °C and 7.4 g/L, respectively). The higher salinity of Levagnole springs is due to a longer interaction with evaporite material embedded in Miocene sedimentary formations and to the eventual mixing, during rising, with fresh seawater close to the seashore. The chemical and isotopic composition of the free gases associated with the springs, again suggests a different source of the two hydrothermal systems. Comparing the 3He/4He measured ratios with other gas emissions located NE and SE of Mt. Massico-Roccamonfina alignment, it is evident that the Levagnole thermal springs are related to the northern Latial mantle wedge where the 3He/4He is about 0.5 R/Ra, whereas the Padule-S. Rocco springs, although being only 3.5 km south of Levagnole, are related to the Campanian mantle wedge where R/Ra is always ≥2.0. Such a difference in 3He/4He ratio in a very short distance

  10. 微波水热法制备CdS纳米晶体的研究%Semiconductor Nanocrystals CdS Synthesized by Microwave-Hydrothermal Method

    Institute of Scientific and Technical Information of China (English)

    王悦虹; 刘岩

    2012-01-01

    利用微波水热技术合成CdS半导体纳米晶体,可以克服有机合成方法毒性大,成本高等问题,通过XRD、TEM表征,产物CdS半导体纳米晶体具有立方晶相,纯度较高。通过紫外吸收光谱和荧光光谱分析,发现该方法制备出的半导体CdS纳米晶体具有良好的光致发光性质,证明水相同样适合高质量CdS半导体纳米晶体的生长。%CdS semiconductor nanocrystals(NCs) were synthesized by microwave-hydrothermal method in water solution.In comparison,with the synthesis of NCs in organic solvents,the growth surroundings of aqueous NCs were more poisonous and costly.The XRD and TEM provided direct evidence for a cubic zinc blende structure of bulk CdS crystal.Moreover,the CdS NCs had excellent photoluminescence properties by the characterizations of absorption spectra and luminescence spectra.This method proved that CdS NCs suited to grow in aqueous condition.

  11. Effect of Reaction Period on Stoichiometry, Phase Purity, and Morphology of Hydrothermally Synthesized Cu2NiSnS4 Nanopowder

    Science.gov (United States)

    Babu, G. Sahaya Dennish; Shajan, X. Sahaya; Alwin, S.; Ramasubbu, V.; Balerao, Gopal M.

    2017-09-01

    The effect of reaction period on the phase purity, morphology, and stoichiometry of Cu2NiSnS4 (CNTS) nanopowder prepared by hydrothermal method has been investigated. Polyvinylpyrrolidone (PVP) and thioglycolic acid were used as capping agent and sulfur source, respectively. The presence of cubic stannite crystal structure and its phase purity were confirmed by powder x-ray diffraction analysis and Raman spectroscopy. Furthermore, the morphological, crystallographic, and optical features of the prepared CNTS nanopowder were characterized by field-emission scanning electron microscopy, transmission electron microscopy, and ultraviolet-visible (UV-Vis) spectrophotometry. The elemental ratios of Cu/(Ni + Sn) and Ni/Sn showed that the stoichiometry of CNTS was maintained for the compounds synthesized at 230°C with reaction period of 24 h. The occurrence of Cu+, Ni2+, Sn4+, and S2- was evaluated by x-ray photoelectron spectroscopy. The prepared material was used as counter electrode in a dye-sensitized solar cell (DSSC) as an alternative to platinum (Pt), resulting in conversion efficiency of 0.92%. These results indicate that CNTS is a prospective material to replace conventional Pt-based counter electrodes in DSSCs.

  12. The superior cycling performance of the hydrothermal synthesized carbon-coated ZnO as anode material for zinc-nickel secondary cells

    Science.gov (United States)

    Feng, Zhaobin; Yang, Zhanhong; Huang, Jianhang; Xie, Xiaoe; Zhang, Zheng

    2015-02-01

    Carbon-coated ZnO is synthesized by the hydrothermal method. The X-ray diffraction (XRD), scanning electron microscope (SEM), high resolution transmission electron microscopy (HRTEM) and energy dispersive X-ray analysis (EDX) tests indicate that carbon is uniformly coated on the surface of the ZnO particle. And the crystal form of ZnO isn't changed. The effects of carbon layer on the electrochemical performances of ZnO have also been investigated by the charge/discharge cycling test, cyclic voltammetry (CV), Tafel polarization curves and electrochemical impedance spectroscope (EIS) tests. The CV curves at different scan rates exhibit that carbon-coated ZnO has the superior reversibility at high scan rate. The charge/discharge cycling tests under different charge/discharge rates show, even if at high-rate, the cycling performance and specific discharge capacity of carbon-coated ZnO are also superior to that of bare ZnO. The Tafel polarization curves and electrochemical impedance spectroscope (EIS) verify that the carbon layer can improve the anti-corrosion and charge-transfer performances of ZnO. The different rate experiments indicate that, compared with the increase of the conductivity, the effect of carbon layer on improving the anti-corrosion performance of ZnO plays a more dominating role in improving the electrochemical performances of ZnO at low charge/discharge rate.

  13. Syntheses of optically efficient (La{sub 1-x-y}Ce{sub x}Tb{sub y})F{sub 3} nanocrystals via a hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Wang Qiang [Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ 08544 (United States); You Yumin; Ludescher, Richard D. [Department of Food Science, Rutgers University, New Brunswick, NJ 08901 (United States); Ju Yiguang, E-mail: yju@princeton.ed [Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ 08544 (United States)

    2010-06-15

    Optically efficient cerium and terbium doped lanthanide fluoride (La{sub 1-x-y}Ce{sub x}Tb{sub y})F{sub 3} nanocrystals with different doping concentrations have been synthesized by a hydrothermal route in the presence of ethylenediamine tetraacetic acid disodium salt (EDTA). The results showed that the formation of nanocrystals with different morphologies depends on terbium ion Tb{sup 3+} doping concentration, but independent of cerium ion Ce{sup 3+} doping concentration. With increase in Tb{sup 3+} doping concentration, the morphologies of nanocrystals evolved from a spherical shape to a plated-like one. In addition, both the photoluminescence quantum yield (PL QY) and the fluorescence lifetime of nanocrystals increased with the increase in Ce{sup 3+} doping concentration in cerium and terbium co-doped system. The PL QY reached up to 55%, and the lifetime up to 7.3 ms. Transmission electron microscopy (TEM), X-ray diffraction (XRD), selected area electron diffraction (SAED), X-ray fluorescence (XRF), energy dispersive spectroscopy (EDS), ultraviolet-visible (UV-vis) absorption, photoluminescence (PL) and infrared (IR) spectroscopies were employed to characterize the properties of nanocrystals. The growth mechanism of nanocrystals with different morphologies and optical properties of nanocrystals with different doping concentrations were investigated.

  14. A colloidal assembly approach to synthesize magnetic porous composite nanoclusters for efficient protein adsorption

    Science.gov (United States)

    Yang, Qi; Lan, Fang; Yi, Qiangying; Wu, Yao; Gu, Zhongwei

    2015-10-01

    A combination strategy of the inverse emulsion crosslinking approach and the colloidal assembly technique is first proposed to synthesize Fe3O4/histidine composite nanoclusters as new-type magnetic porous nanomaterials. The nanoclusters possess uniform morphology, high magnetic content and excellent protein adsorption capacity, exhibiting their great potential for bio-separation.A combination strategy of the inverse emulsion crosslinking approach and the colloidal assembly technique is first proposed to synthesize Fe3O4/histidine composite nanoclusters as new-type magnetic porous nanomaterials. The nanoclusters possess uniform morphology, high magnetic content and excellent protein adsorption capacity, exhibiting their great potential for bio-separation. Electronic supplementary information (ESI) available: Experimental details. See DOI: 10.1039/c5nr05800g

  15. Thermal Conductivity of Epoxy Resin Composites Filled with Combustion Synthesized h-BN Particles.

    Science.gov (United States)

    Chung, Shyan-Lung; Lin, Jeng-Shung

    2016-05-20

    The thermal conductivity of epoxy resin composites filled with combustion-synthesized hexagonal boron nitride (h-BN) particles was investigated. The mixing of the composite constituents was carried out by either a dry method (involving no use of solvent) for low filler loadings or a solvent method (using acetone as solvent) for higher filler loadings. It was found that surface treatment of the h-BN particles using the silane 3-glycidoxypropyltrimethoxysilane (GPTMS) increases the thermal conductivity of the resultant composites in a lesser amount compared to the values reported by other studies. This was explained by the fact that the combustion synthesized h-BN particles contain less -OH or active sites on the surface, thus adsorbing less amounts of GPTMS. However, the thermal conductivity of the composites filled with the combustion synthesized h-BN was found to be comparable to that with commercially available h-BN reported in other studies. The thermal conductivity of the composites was found to be higher when larger h-BN particles were used. The thermal conductivity was also found to increase with increasing filler content to a maximum and then begin to decrease with further increases in this content. In addition to the effect of higher porosity at higher filler contents, more horizontally oriented h-BN particles formed at higher filler loadings (perhaps due to pressing during formation of the composites) were suggested to be a factor causing this decrease of the thermal conductivity. The measured thermal conductivities were compared to theoretical predictions based on the Nielsen and Lewis theory. The theoretical predictions were found to be lower than the experimental values at low filler contents ( 60 vol %).

  16. Thermal Conductivity of Epoxy Resin Composites Filled with Combustion Synthesized h-BN Particles

    Directory of Open Access Journals (Sweden)

    Shyan-Lung Chung

    2016-05-01

    Full Text Available The thermal conductivity of epoxy resin composites filled with combustion-synthesized hexagonal boron nitride (h-BN particles was investigated. The mixing of the composite constituents was carried out by either a dry method (involving no use of solvent for low filler loadings or a solvent method (using acetone as solvent for higher filler loadings. It was found that surface treatment of the h-BN particles using the silane 3-glycidoxypropyltrimethoxysilane (GPTMS increases the thermal conductivity of the resultant composites in a lesser amount compared to the values reported by other studies. This was explained by the fact that the combustion synthesized h-BN particles contain less –OH or active sites on the surface, thus adsorbing less amounts of GPTMS. However, the thermal conductivity of the composites filled with the combustion synthesized h-BN was found to be comparable to that with commercially available h-BN reported in other studies. The thermal conductivity of the composites was found to be higher when larger h-BN particles were used. The thermal conductivity was also found to increase with increasing filler content to a maximum and then begin to decrease with further increases in this content. In addition to the effect of higher porosity at higher filler contents, more horizontally oriented h-BN particles formed at higher filler loadings (perhaps due to pressing during formation of the composites were suggested to be a factor causing this decrease of the thermal conductivity. The measured thermal conductivities were compared to theoretical predictions based on the Nielsen and Lewis theory. The theoretical predictions were found to be lower than the experimental values at low filler contents (< 60 vol % and became increasing higher than the experimental values at high filler contents (> 60 vol %.

  17. 微波辅助加热粉煤灰水热合成沸石的最佳条件%The Better Condition for Hydrothermal Synthesizing Zeolite from Coal Fly Ash under the Microwave

    Institute of Scientific and Technical Information of China (English)

    崔红梅; 柯灵非; 李芳; 齐晗兵; 康媞

    2012-01-01

    The zeolite was synthesized by hydrothermal method under the microwave using the coal fly ash as the material. The synthesis effect of zeolite was detected with cation exchange capacity. The synthesis technologies of zeolite under the microwave were compared with conventional synthesis under the same conditions. The impact factor and the best condition of this method was discussed. The main factor which influences the category of synthesized zeolite and rate were chemical compositions of coal fly ash, temperature, time, activator, concentration of alkali, ratio of solution and solid, microwave, etc. The best conditions were 120 ℃ ,40 min,2 mol/L NaOH,ratio of solution and solid 2.5.%以火力发电厂粉煤灰为原料,微波辅助加热水热合成沸石,并用阳离子交换容量(CEC)检测粉煤灰沸石合成效果.将微波辅助加热合成与同等条件下的常规水热合成进行比较,探讨微波辅助合成沸石中的影响因素及最佳条件.微波条件下影响粉煤灰合成沸石的种类及合成效果的主要因素有:粉煤灰的组分、温度、时间、活化剂种类、碱浓度、液固比、微波催化等;微波合成最佳条件为:120℃、40 min、NaOH浓度2 mol/L、液固比2.5.

  18. Synthesize of AZ31/TiC magnesium matrix composites using friction stir processing

    Directory of Open Access Journals (Sweden)

    M. Balakrishnan

    2015-03-01

    Full Text Available Friction stir processing (FSP is a novel solid state technique to synthesize metal matrix composites. In the present work, an attempt has been made to synthesize AZ31/TiC magnesium matrix composites using FSP and to analyze the microstructure using scanning electron microscopy. A groove was prepared on 6 mm thick AZ31 magnesium alloy plates and compacted with TiC particles. The width of the groove was varied to result in four different volume fraction of TiC particles (0, 6, 12 and 18 vol.%. A single pass FSP was carried out using a tool rotational speed of 1200 rpm, traverse speed of 40 mm/min and an axial force of 10 kN. Scanning electron microscopy was employed to study the microstructure of the synthesized composites. The results indicated that TiC particles were distributed uniformly in the magnesium matrix without the formation of clusters. There was no interfacial reaction between the magnesium matrix and the TiC particle. TiC particles were properly bonded to the magnesium matrix.

  19. Efficient photocatalytic removal of nitric oxide with hydrothermal synthesized Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Ai, Zhihui, E-mail: jennifer.ai@mail.ccnu.edu.cn; Lu, Gang; Lee, Shuncheng

    2014-11-15

    Highlights: • Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} nanotubes were prepared via a facile hydrothermal route. • The Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} nanotubes exhibited superior photocatalytic performances for the removal of nitric oxide. • The Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} nanotubes show potential for indoor and outdoor air purification. - Abstract: In this study, Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} nanotubes were synthesized with a facile hydrothermal method using TiO{sub 2} P25 (Degussa) and bismuth citrate (BiC{sub 5}H{sub 6}O{sub 7}) as precursors in concentrated NaOH and ammonia alkali solution. The samples were systematically characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The as-prepared Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} nanotubes exhibited superior activity for photocatalytic removal of gaseous nitric oxide (NO) over TiO{sub 2} P25 (Degussa) under simulated solar-light irradiation, the NO removal rate can reach as high as ca. 200 ppb·min{sup −1} over the Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} nanotubes in a continuous reactor with an initial NO concentration of 400 ppb. The intrinsic hollow-nanotube structure of the Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} photocatalysts contributes to its superior activity under simulated solar light. This work provides a facile route to prepare Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} nanotubes and suggests that the Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} nanotubes are ideal candidates for efficient removal of nitric oxide in indoor/outdoor air.

  20. Defluoridation using biomimetically synthesized nano zirconium chitosan composite: Kinetic and equilibrium studies

    Energy Technology Data Exchange (ETDEWEB)

    Prasad, Kumar Suranjit, E-mail: suranjit@gmail.com [Department of Environmental Biotechnology, Ashok and Rita Patel Institute of Integrated Study and Research in Biotechnology and Allied Sciences (ARIBAS), New Vallabh Vidyanagar, Anand, 388121 Gujarat (India); Amin, Yesha, E-mail: yesha_2879@yahoo.co.in [Department of Environmental Biotechnology, Ashok and Rita Patel Institute of Integrated Study and Research in Biotechnology and Allied Sciences (ARIBAS), New Vallabh Vidyanagar, Anand, 388121 Gujarat (India); Selvaraj, Kaliaperumal, E-mail: k.selvaraj@ncl.res.in [Nano and Computational Materials Lab, Catalysis Division, National Chemical Laboratory, Council of Scientific and Industrial Research, Pune 411008 (India)

    2014-07-15

    Highlights: • Colloidal Zr nanoparticles, synthesized using Aloe vera extract were entrapped in chitosan beads. • Zr loaded beads were employed for removal of F{sup −} ion and showed excellent removal efficiency. • Zr and chitosan are cost effective materials hence can be a good adsorbent for removal of fluoride. - Abstract: The present study reports a novel approach for synthesis of Zr nanoparticles using aqueous extract of Aloe vera. Resulting nanoparticles were embedded into chitosan biopolymer and termed as CNZr composite. The composite was subjected to detailed adsorption studies for removal of fluoride from aqueous solution. The synthesized Zr nanoparticles showed UV–vis absorption peak at 420 nm. TEM result showed the formation of polydispersed, nanoparticles ranging from 18 nm to 42 nm. SAED and XRD analysis suggested an fcc (face centered cubic) Zr crystallites. EDAX analysis suggested that Zr was an integral component of synthesized nanoparticles. FT-IR study indicated that functional group like -NH, -C=O, -C=N and -C=C were involved in particle formation. The adsorption of fluoride on to CNZr composite worked well at pH 7.0, where ∼99% of fluoride was found to be adsorbed on adsorbent. Langmuir isotherm model best fitted the equilibrium data since it presented higher R{sup 2} value than Freundlich model. In comparison to pseudo-first order kinetic model, the pseudo-second order model could explain adsorption kinetic behavior of F{sup −} onto CNZr composite satisfactorily with a good correlation coefficient. The present study revealed that CNZr composite may work as an effective tool for removal of fluoride from contaminated water.

  1. Some studies on ceria–zirconia reinforced solvothermally synthesized cordierite nano-composites

    Energy Technology Data Exchange (ETDEWEB)

    Srivastava, Abhinav, E-mail: srivasabhinav@gmail.com; Singh, Vinay Kumar; Kumar, Vijay; Hemanth Kumar, P.; Tripathi, Himanshu; Chaudhary, Ashish; Asiwal, Krit; Pandey, Rahul; Suman, Shyam Kumar

    2014-02-15

    Graphical abstract: -- Highlights: • Nanocordierite synthesized through solvo-thermal process. • [CeO{sub 2(0.12)}]⋅[ZrO{sub 2(0.88)}] processed by gelation and co-precipitation method. • The effect of mineralizer addition on cordierite formation was studied. • Investigation of thermo-mechanical properties of prepared nano-composites. -- Abstract: Nanostructured cordierite and 12 mol% ceria stabilized zirconia were chemically prepared separately. Pure cordierite was synthesized solvothermally, whereas [(Zr){sub 0.88}(Ce){sub 0.12}O{sub 2}] termed as CeSZ was processed with gelation and co-precipitation method. The evolution of crystalline phases and the microstructures have been studied using X-ray diffractometer, and FE-SEM with EDX. Varying contents (0–20 weight%) of CeSZ were then mixed with cordierite to form sample blocks of desired shapes. These nano-composite blocks were fired at 1100–1400 °C for a soaking time of 3 h to observe their thermo-mechanical, micro-structural and physical properties. Results indicate that ceria not only acts as a stabilizer in zirconia ceramics but it also acts as a sintering aid in cordierite formation. CeO{sub 2} also improves compressibility and structural properties of nano-composites. Sintering temperature also plays an important role in the behavior of nano-composite blocks. All properties show a major improvement than previous reported data’s.

  2. Water defluoridation using a nanostructured diatom-ZrO₂ composite synthesized from algal biomass.

    Science.gov (United States)

    Thakkar, Megha; Wu, Zheqiong; Wei, Liping; Mitra, Somenath

    2015-07-15

    Frustules or the rigid amorphous silica cell wall of unicellular, photosynthetic microalgae with unique porous architecture has been used to synthesize a composite by immobilizing ZrO2 on its surface and in the pores. This was effective in water defluoridation. The average diameter of the composite was 80±2 nm and surface area was 140 m(2)/g. The adsorption isotherms followed both Langmuir and Freundlich models, and the composite was regenerable. Adsorption kinetics followed second order model and the adsorption capacity was as high as 11.32 mg/g, while the Langmuir maximum adsorption capacity (q(m)) reached 15.53 mg/g. The research findings highlight the potential of diatoms as hosts for nanomaterials for use in water treatment. Copyright © 2015 Elsevier Inc. All rights reserved.

  3. Photocatalytic Degradation of Rhodamine B Dye with MWCNT/TiO2/C60 Composites by a Hydrothermal Method

    Institute of Scientific and Technical Information of China (English)

    SHI Xiaoliang; YANG Xingyong; WANG Shuwei; WANG Sheng; ZHANG Qiaoxin; WANG Yufu

    2011-01-01

    Multi-walled carbon nanotube (MWCNT)/TiO2/C60 composite catalysts were prepared by hydrothermal method. TiO2 was deposited on the MWCNT surface. Their photocatalytic activities for degradation of Rhodamine B dye were studied. X-ray diffraction, field emission transmission electron microscopy, ultraviolet-visible light absorption spectrum and photoluminescence spectrum were carried out to characterize the composite catalysts. The results indicated that MWCNTs and C6o could greatly enhance the photocatalytic activity of TiO2.

  4. Highly Sulfonated Diamine Synthesized Polyimides and Protic Ionic Liquid Composite Membranes Improve PEM Conductivity

    Directory of Open Access Journals (Sweden)

    Bor-Kuan Chen

    2015-06-01

    Full Text Available A novel sulfonated diamine was synthesized from 1,4-bis(4-aminophenoxy benzene [pBAB]. Sulfonated polyimides (SPIs were synthesized from sulfonated pBAB, 1,4-bis(4-aminophenoxy-2-sulfonic acid benzenesulfonic acid [pBABTS], various diamines and aromatic dianhydrides. Composite proton exchange membranes (PEMs made of novel SPIs and a protic ionic liquid (PIL 1-vinyl-3-H-imidazolium trifluoromethanesulfonate [VIm][OTf] showed substantially increased conductivity. We prepared an SPI/PIL composite PEM using pBABTS, 4,4′-(9-fluorenylidene dianiline (9FDA as diamine, 3,3′,4,4′-diphenylsulfone tetracarboxylic dianhydride (DSDA as dianhydride and 40 wt % [VIm][OTf] with a high conductivity of 16 mS/cm at 120 °C and anhydrous condition. pBABTS offered better conductivity, since the chemical structure had more sulfonated groups that provide increased conductivity. The new composite membrane could be a promising anhydrous or low-humidity PEM for intermediate or high-temperature fuel cells.

  5. Elemental and isotopic compositions of the hydrothermal sulfide on the East Pacific Rise near 13°N

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The mineralogical,elemental,and isotopic characteristics of a hydrothermal sulfide sample from one dredge station (12°42.30’N,103°54.48’W,water depth 2655 m) on the East Pacific Rise near 13°N were analyzed.The hydrothermal sulfide was composed mainly of sphalerite,chalcopyrite,and pyrite and was a Zn-rich sulfide;in layer ep-s-1,goethite formed by secondary oxidation was found.The concentrations of rare elements,such as Li (0.15×10-6-0.30×10-6),Be (0.01×10-6-0.05×10-6),Zr (73.8×10-9-1344×10-9),Nb (8.14×10-9-64.7×10-9),Hf (2.54×10-9-28.0×10-9),and Ta (0.203×10-9-1.21×10-9),were far lower in the hydrothermal sulfide than in the ocean crust,whereas the content of Au was higher and the contents of Co,Ni,Sr,Cs,Ba,Bi,and U were low.The correlations between Zn and Cr,Cd and Ga,Cu and P,P and In (R2 > 0.8) were positive,whereas those between Zn and Fe,Cu,and Ba (R2 > 0.8) were distinctly negative.From low-temperature mineral assemblages to high-temperature mineral assemblages,the spatial distributions of dispersive and rare elements (e.g.In,Li,Cs) in the hydrothermal sulfide displayed corresponding variations.The variations observed in some elements (e.g.,Cd,Cs,P) are controlled by Zn,Fe,and Cu sulfides,respectively.Seafloor weathering accounts for the enrichment of V,Mn,and rare earth elements (REE) in the henna sulfide-oxidation layer that bears the secondary oxide mineral,leading to identical REE patterns for this layer (ep-s-1) and seawater.Seafloor weathering also distinctly affects the correlations between the element ratios of the hydrothermal sulfide.From high-temperature mineral assemblages to low-temperature mineral assemblages,Fe content and δ 34S value of the hydrothermal sulfide increase gradually,and Zn content and lead isotopic ratios decrease gradually on the contrary,which indicate the influences of seawater on elements and the sulfur and lead isotopic compositions enhance gradually during the formation of hydrothermal sulfides.

  6. The role of hydrothermally prepared supported photocatalytic composite in organic micro-pollutants removal from the water.

    Science.gov (United States)

    Shivaraju, H P; Byrappa, K

    2012-07-01

    This work deals with the non-biodegradable micro-pollutants degradation by supported photocatalyst based heterogeneous photocatalytic reaction. TiO2 based supported photocatalyst was prepared by the hydrothermal technique to improve the photocatalytic performance along with easy recovery of suspended photocatalyst from aqueous medium after photoreaction. TO2 deposited calcium alumino-silicate beads (CASB) supports were prepared under mild hydrothermal conditions (Temparature-200 degrees C, Duration-24 h). In the present study, industrial dyes such as Amaranth and Brilliant Yellow were used as model micro-pollutants in aqueous solution. A real time pesticide industrial effluent was tested for its photocatalytic removal of organic pollutants using TO2 deposited CASB supported photocatalytic composite as an effective photocatalyst. Photocatalytic degradation of micro-pollutants present in aqueous medium was carried out in a batch photoreactor, at atmospheric pressure and temperature (28 degrees C). The influence of different light sources, irradiation time, catalyst load and catalytic performance is discussed. The photocatalytic degradation of micro-pollutants in aqueous medium was evaluated by determination of COD and %T. Easy separation and recovery of suspended photocatalysts from aqueous solution is the major advantage of hydrothermally prepared supported photocatalytic composite.

  7. Enhanced lithium storage in a VO{sub 2}(B)-multiwall carbon nanotube microsheet composite prepared via an in situ hydrothermal process

    Energy Technology Data Exchange (ETDEWEB)

    Rahman, M.M., E-mail: mmr543@uow.edu.a [Institute for Superconducting and Electronic Materials and ARC Centre of Excellence for Electromaterials Science, University of Wollongong, NSW 2522 (Australia); Wang Jiazhao [Institute for Superconducting and Electronic Materials and ARC Centre of Excellence for Electromaterials Science, University of Wollongong, NSW 2522 (Australia); Idris, Nurul Hayati [Institute for Superconducting and Electronic Materials and ARC Centre of Excellence for Electromaterials Science, University of Wollongong, NSW 2522 (Australia); Department of Science Physics, University of Malaysia Terengganu, Kuala Terengganu 20522 (Malaysia); Chen Zhixin [School of Mechanical, Mechatronic and Materials Engineering, University of Wollongong, NSW 2522 (Australia); Liu Huakun [Institute for Superconducting and Electronic Materials and ARC Centre of Excellence for Electromaterials Science, University of Wollongong, NSW 2522 (Australia)

    2010-12-30

    A novel VO{sub 2}(B)-multiwall carbon nanotube (MWCNT) composite with a sheet-like morphology was synthesized by a simple in situ hydrothermal process. The morphology and structural properties of the samples were investigated by X-ray diffraction (XRD), thermogravimetric analysis (TGA), field emission scanning electron microscopy (FE-SEM), and transmission electron microscopy (TEM). FE-SEM observations demonstrated that the nanosheets are frequently grown together in the form of bundles composed of numerous nanosheets, each with a smooth surface and a typical length of 300-500 nm, width of 50-150 nm, and thickness of 10-50 nm. Electrochemical measurements were carried out using different discharge cut-off voltages. Electrochemical tests show that the VO{sub 2}(B)-MWCNT composite cathode features long-term cycling stability and high discharge capacity (177 mAh g{sup -1}) in the voltage range of 2.0-3.25 V at 1 C with a capacity retention of 92% after 100 cycles. The electrochemical impedance spectra (EIS) indicate that the VO{sub 2}(B)-MWCNT composite electrode has very low charge-transfer resistance compared with pure VO{sub 2}(B), indicating the enhanced ionic conductivity of the VO{sub 2}(B)-MWCNT composite. The enhanced cycling stability is attributed to the fact that the VO{sub 2}(B)-MWCNT composite can prevent the aggregation of active materials, accommodate the large volume variation, and maintain good electronic contact. We strongly believe that the VO{sub 2}(B)-MWCNT composite can be considered as a potential cathode material for lithium-ion batteries.

  8. Electrochemical characteristics of Sn-Al-P-B composites synthesized by rheological technique

    Institute of Scientific and Technical Information of China (English)

    HE Ze-qiang; MA Ming-you; XIAO Zhuo-bing; XIONG Li-zhi; CHEN Shang; WU Xian-ming

    2006-01-01

    Sn-Al-P-B composites were synthesized by novel rheological technique. The microstructure, morphology, and electrochemical performance of the materials were investigated by X-ray diffraction, scanning electron microscopy and electrochemical methods. The particles of tin oxide-based materials form an interconnected network structure like mesoporous materials. The average size of the particles is about 150 nm. The material delivers a charge capacity of more than 570 mA·h/g. The capacity retention of the material is about 95.5% after being cycled 30 times. The good electrochemical performance indicates that this kind of tin oxide-based material is promising anode for lithium ion battery.

  9. A comparison study of polymer/cobalt ferrite nano-composites synthesized by mechanical alloying route

    Directory of Open Access Journals (Sweden)

    Sedigheh Rashidi

    2015-12-01

    Full Text Available In this research, the effect of different biopolymers such as polyethylene glycol (PEG and polyvinylalcohol (PVA on synthesis and characterization of polymer/cobalt ferrite (CF nano-composites bymechanical alloying method has been systematically investigated. The structural, morphological andmagnetic properties changes during mechanical milling were investigated by X-ray diffraction (XRD,Fourier transform infrared spectroscopy (FTIR, transmission electron microscopy (TEM, fieldemission scanning electron microscopy (FESEM, and vibrating sample magnetometer techniques(VSM, respectively. The polymeric cobalt ferrite nano-composites were obtained by employing atwo-step procedure: the cobalt ferrite of 20 nm mean particle size was first synthesized by mechanicalalloying route and then was embedded in PEG or PVA biopolymer matrix by milling process. Theresults revealed that PEG melted due to the local temperature raise during milling. Despite thisphenomenon, cobalt ferrite nano-particles were entirely embedded in PEG matrix. It seems, PAV is anappropriate candidate for producing nano-composite samples due to its high melting point. InPVA/CF nano-composites, the mean crystallite size and milling induced strain decreased to 13 nm and0.48, respectively. Moreover, milling process resulted in well distribution of CF in PVA matrix eventhough the mean particle size of cobalt ferrite has not been significantly affecetd. FTIR resultconfirmed the attachment of PVA to the surface of nano-particles. Magnetic properties evaluationshowed that saturation magnetization and coercivity values decreased in nano-composite samplecomparing the pure cobalt ferrite.

  10. Synthesizing Service Composition Models on the Basis of Temporal Business Rules

    Institute of Scientific and Technical Information of China (English)

    Jian Yu; Yan-Bo Han; Jun Han; Yan Jin; Paolo Falcarin; Maurizio Morisio

    2008-01-01

    Transformational approaches to generating design and implementation models from requirements can bring effectiveness and quality to software development. In this paper we present a framework and associated techniques to generate the process model of a service composition from a set of temporal business rules. Dedicated techniques including pathfinding, branching structure identification and parallel structure identification are used for semi-automatically synthesizing the process model from the semantics-equivalent Finite State Automata of the rules. These process models naturally satisfy the prescribed behavioral constraints of the rules. With the domain knowledge encoded in the temporal business rules,an executable service composition program, e.g., a BPEL program, can be further generated from the process models. A running example in the e-business domain is used for illustrating our approach throughout this paper.

  11. Phase composition of cathodic deposits synthesized in flinak-k2taf7-kbf4 melt

    Directory of Open Access Journals (Sweden)

    Makarova O.V.

    2003-01-01

    Full Text Available The phase composition of cathodic deposits synthesized from FLINAK-K2TaF7-KBF4 melt has been studied by the X-ray diffraction method. It is shown that boron content in the electrodeposit grows as the cathodic potential is increased from peak R1 to peak R4 in the voltammogram. The scheme of changes in the phase composition depending on the increasing current density is given as follows: {β-Ta + Ta2B}R1 → {β-Ta + (Ta3B4 TaB}R2 → {TaB2}R3 → {TaB2 + B}R4.

  12. A Novel FCC Catalyst Based on a Porous Composite Material Synthesized via an In Situ Technique

    Directory of Open Access Journals (Sweden)

    Shu-Qin Zheng

    2015-11-01

    Full Text Available To overcome diffusion limitations and improve transport in microporous zeolite, the materials with a wide-pore structure have been developed. In this paper, composite microspheres with hierarchical porous structure were synthesized by an in situ technique using sepiolite, kaolin and pseudoboehmite as raw material. A novel fluid catalytic cracking (FCC catalyst for maximizing light oil yield was prepared based on the composite materials. The catalyst was characterized by XRD, FT-IR, SEM, nitrogen adsorption-desorption techniques and tested in a bench FCC unit. The results indicated that the catalyst had more meso- and macropores and more acid sites than the reference catalyst, and thus can increase light oil yield by 1.31 %, while exhibiting better gasoline and coke selectivity.

  13. Hydrothermal synthesis of reduced graphene sheets/Fe2O3 nanorods composites and their enhanced electrochemical performance for supercapacitors

    Science.gov (United States)

    Yang, Wanlu; Gao, Zan; Wang, Jun; Wang, Bin; Liu, Lianhe

    2013-06-01

    Reduced graphene nanosheets/Fe2O3 nanorods (GNS/Fe2O3) composite has been fabricated by a hydrothermal route for supercapacitor electrode materials. The obtained GNS/Fe2O3 composite formed a uniform structure with the Fe2O3 nanorods grew on the graphene surface and/or filled between the graphene sheets. The electrochemical performances of the GNS/Fe2O3 hybrid supercapacitor were tested by cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic charge-discharge tests in 6 M KOH electrolyte. Comparing with the pure Fe2O3 electrode, GNS/Fe2O3 composite electrode exhibits an enhanced specific capacitance of 320 F g-1 at 10 mA cm-2 and an excellent cycle-ability with capacity retention of about 97% after 500 cycles. The simple and cost-effective preparation technique of this composite with good capacitive behavior encourages its potential commercial application.

  14. Sulfur isotopic composition of seafloor hydrothermal sediment from the Jade hydrothermal field in the central Okinawa Trough and its geological significance

    Institute of Scientific and Technical Information of China (English)

    曾志刚; 李军; 蒋富清; 翟世奎; 秦蕴珊; 侯增谦

    2002-01-01

    --Eighteen samples of hydrothermal sediments from the Jade hydrotherrnal field in the central Okinawa Trough have been analyzed. Sulfur isotopic values for 10 sulfide samples vary from 5.2 ×10-3to 7.2× 10-3, δ34S valUes for 7 sulfate samples vary from 16.3 × 10-3 to 22.3 × 10-3, and 1 native sulphur sample has a δ34S value of 8.2 × 10-3. The major sources of sulfur for hydrothermal sediment are intermediate to acid volcanic rocks and sea water sulfate, and it is possible that the partial sulfur of hydrothermal sediment is from the pelagic sediment by the interaction between hydrothermal fluid and sediment. The reasons of causing the distinct differences in sulfur isotopic values for sulfide samples from hydrothermal sediment ( compared with other hydrothermal fields), are the differences in the sources of sulfur, the magmatic activity and the tectonic evolution in different hydrothermal fields. The sulfur evolution is a long and complex process in the seafloor hydrothermal system, involving the ascending of heating sea water, the interaction between fluid and volcanic rocks, the mixing of sea water sulfate and sulfur from intermediate to acid volcanic rocks, and the fluid/pelagic-sediment interaction. And the interaction between sea water and intermediate to acid volcanic rocks is an important mechanism for the sulfur evolution in the Jade hydrothermal field.

  15. Comparative study of the ZnO and Zn{sub 1-x}Cd{sub x}O nanorod emitters hydrothermally synthesized and electrodeposited on p-GaN

    Energy Technology Data Exchange (ETDEWEB)

    Lupan, O., E-mail: lupan@physics.ucf.edu [Department of Physics, University of Central Florida, PO Box 162385 Orlando, FL 32816-2385 (United States); Laboratoire d' Electrochimie, Chimie des Interfaces et Modelisation pour l' Energie (LECIME) UMR-7575, ENSCP-Chimie Paristech, 11 rue Pierre et Marie Curie, 75231 Paris, cedex 05 (France); Department of Microelectronics and Semiconductor Devices, Technical University of Moldova, 168 Stefan cel Mare Blvd., MD-2004, Chisinau (Moldova, Republic of); Pauporte, T., E-mail: thierry-pauporte@chimie-paristech.fr [Laboratoire d' Electrochimie, Chimie des Interfaces et Modelisation pour l' Energie (LECIME) UMR-7575, ENSCP-Chimie Paristech, 11 rue Pierre et Marie Curie, 75231 Paris, cedex 05 (France); Chow, L.; Chai, G. [Department of Physics, University of Central Florida, PO Box 162385 Orlando, FL 32816-2385 (United States); Viana, B. [Laboratoire de Chimie de la Matiere Condensee de Paris, UMR 7574, ENSCP, 11 rue P. et M. Curie, 75231 Paris cedex 05 (France); Ursaki, V.V. [Institute of Electronic Engineering and Nanotechnologies, Institute of Applied Physics, Academy of Sciences of Moldova, MD-2028 Chisinau (Moldova, Republic of); Monaico, E. [Department of Microelectronics and Semiconductor Devices, Technical University of Moldova, 168 Stefan cel Mare Blvd., MD-2004, Chisinau (Moldova, Republic of); Institute of Electronic Engineering and Nanotechnologies, Institute of Applied Physics, Academy of Sciences of Moldova, MD-2028 Chisinau (Moldova, Republic of); Tiginyanu, I.M. [Institute of Electronic Engineering and Nanotechnologies, Institute of Applied Physics, Academy of Sciences of Moldova, MD-2028 Chisinau (Moldova, Republic of)

    2012-10-15

    Highlights: Black-Right-Pointing-Pointer Rapid hydrothermal seed layer-free synthesis (15 min) of epitaxial ZnO and n-Zn{sub 1-x}Cd{sub x}O nanorod arrays on p-GaN(0 0 0 1). Black-Right-Pointing-Pointer The effects of hydrothermal versus electrochemical deposition synthesis on the optical properties of ZnO nanorods on GaN substrate are reported in details. Black-Right-Pointing-Pointer The hetero-structures were used for LED applications. With hydrothermal-ZnO and electrodeposited-ZnO, UV-emission started at low forward voltage of 3.9-4.0 V and 4.4 V. Black-Right-Pointing-Pointer It was demonstrated that a single short wavelength emission shifted to the violet range with Cd-alloying of ZnO nanorods by hydrothermal technique. - Abstract: Hydrothermal synthesis and electrodeposition are low-temperature and cost-effective growth techniques of high quality nanostructured active materials for opto-electronic devices. Here we report a hydrothermal seed layer-free and rapid synthesis (15 min) of epitaxial nanorod arrays of ZnO on p-GaN(0 0 0 1). The effects of hydrothermal (HT) versus electrochemical deposition (ECD) synthesis on the optical properties of ZnO nanorods/nanowires on p-GaN substrate are compared in details. For both types of layers, a strong photoluminescent UV-emission was found indicating the high quality of the synthesized ZnO layer. The hetero-structures were used for LED applications. With HT-ZnO and ECD-ZnO, UV-emission started at remarkably low forward voltage of 3.9-4.0 V and 4.4 V respectively and increased rapidly. Moreover, the LED structures showed a stable and repeatable electroluminescence. We propose for further studies a simple, efficient, seed layer-free and low temperature hydrothermal growth technique to fabricate high quality ZnO nanorods/p-GaN heterojunction LED nanodevices. It is also demonstrated that a single short wavelength emission can be shifted to the violet range with Cd-alloying of ZnO used for LED structure.

  16. High-performance Ni[sub 3]Al synthesized from composite powders

    Energy Technology Data Exchange (ETDEWEB)

    Chiou, W.C.; Hu, C.T. (National Tsing Hua Univ., Hsinchu (Taiwan, Province of China). Dept. of Materials Science and Engineering)

    1994-05-01

    Specimens of Ni[sub 3]Al + B of high density (>99.3 pct RD) and relatively large dimension have been synthesized from composite powders through processes of replacing plating and electroless Ni-B plating on Al powder, sintering, and thermal-mechanical treatment. The uniformly coated Ni layer over fine Al or Ni core particles constituting these coating/core composite powders has advantages such as better resistance to oxidation relative to pure Al powder, a greater green density as a compacted powder than prealloyed powder, the possibility of atomically added B to the material by careful choice of a suitable plating solution, and avoidance of the expensive powder metallurgy (PM) equipment such as a hot isostatic press (HIP), hot press (HP), etc. The final Ni[sub 3]Al + B product is made from Ni-B-Al and Ni-B-Ni mixed composite powders by means of traditional PM processes such as compacting, sintering, rolling, and annealing, and therefore, the dimensions of the product are not constrained by the capacity of an HIP or HP. The properties of Ni[sub 3]Al composite powder metallurgy (CPM) specimens tested at room temperature have been obtained, and comparison with previous reports is conducted. A tensile elongation of about 16 pct at room temperature was attained.

  17. Hydrothermal synthesis, characterization and composition-dependent magnetic properties of LaFe 1- xCr xO 3 system (0≤ x≤1)

    Science.gov (United States)

    Hu, Weiwei; Chen, Yan; Yuan, Hongming; Zhang, Ganghua; Li, Guanghua; Pang, Guangsheng; Feng, Shouhua

    2010-07-01

    Hydrothermal synthesis, characterization and magnetic properties of a series of ABO 3-perovskites LaFe 1- xCr xO 3 (0≤ x≤1) are reported. The alkalinity in initial reaction mixtures plays a critical role in controlling the designed stoichiometry of the final compositions. Their magnetic properties are strongly dependent on the compositions and a maximum magnetic moment is found for the sample at x=0.5. Weak ferromagnetic interaction observed for the samples from x=0 to 0.9 arises from the presence of Fe-O-Fe antisymmetric exchange and Fe-O-Cr superexchange interaction. The weak ferromagnetism as well as the linear variation of the lattice parameters implies the possible random distribution of Fe and Cr ions in B sites of the perovskites. The evolution of magnetic ordering transition temperatures has a close relationship with substituent ratios, for the competition of antiferromagnetism and ferromagnetism. The saturated magnetic moment shows a great improvement compared with that for the samples synthesized by solid state method.

  18. Hydrothermal synthesis of graphitic carbon nitride-BiVO4 composites with enhanced visible light photocatalytic activities and the mechanism study

    Science.gov (United States)

    Guo, Feng; Shi, Weilong; Lin, Xue; Che, Guangbo

    2014-11-01

    Novel graphitic carbon nitride (C3N4) and bismuth vanadate (BiVO4) composite photocatalysts were successfully synthesized by a facile hydrothermal method. The scanning electron microscopy (SEM) revealed that an intimate interface between C3N4 and BiVO4 formed in the composites. Compared with the pure C3N4 and BiVO4, the C3N4-BiVO4 photocatalysts showed remarkably the higher photocatalytic activities in degrading rhodamine B (Rh B). The best active heterojunction proportion was 0.5C3N4-0.5BiVO4. Over this catalyst, the 100% degradation of Rh B (0.002 mmol L-1) was obtained under visible light irradiation (λ>420 nm) for 40 min. The active species in Rh B degradation were examined by adding a series of scavengers. The study on photocatalytic mechanism revealed that the electrons injected directly from the conduction band of C3N4 to that of BiVO4, resulting in the production of superoxide radical (O2•-) and hydroxyl radical (OH•) in the conduction band of BiVO4. Simultaneously, the rich holes in the valence band of g-C3N4 oxidized Rh B directly to promote the photocatalytic degradation reaction.

  19. MgCoAl and NiCoAl LDHs synthesized by the hydrothermal urea hydrolysis method: Structural characterization and thermal decomposition

    Energy Technology Data Exchange (ETDEWEB)

    Chagas, L.H., E-mail: lhchagas-prometro@inmetro.gov.br [Universidade Federal de Juiz de Fora, Departamento de Química, Grupo de Físico-Química de Sólidos e Interfaces, 36036-330 Juiz de Fora, MG (Brazil); Instituto Nacional de Metrologia Qualidade e Tecnologia, Divisão de Metrologia de Materiais, 25250-020 Duque de Caxias, RJ (Brazil); De Carvalho, G.S.G.; Do Carmo, W.R. [Universidade Federal de Juiz de Fora, Departamento de Química, Grupo de Físico-Química de Sólidos e Interfaces, 36036-330 Juiz de Fora, MG (Brazil); San Gil, R.A.S. [Universidade Federal do Rio de Janeiro, Instituto de Química, 21949-900 Rio de Janeiro, RJ (Brazil); Chiaro, S.S.X. [PETROBRAS-CENPES, 21941-915 Rio de Janeiro, RJ (Brazil); Leitão, A.A.; Diniz, R. [Universidade Federal de Juiz de Fora, Departamento de Química, Grupo de Físico-Química de Sólidos e Interfaces, 36036-330 Juiz de Fora, MG (Brazil); De Sena, L.A.; Achete, C.A. [Instituto Nacional de Metrologia Qualidade e Tecnologia, Divisão de Metrologia de Materiais, 25250-020 Duque de Caxias, RJ (Brazil)

    2015-04-15

    Highlights: • We synthesized MgCoAl and NiCoAl LDHs by the urea hydrolysis method. • Aluminum rich and crystalline materials have been formed. • The calcination of the LDHs generated mixed oxides with high surface areas. - Abstract: Layered double hydroxides (LDHs) with Mg/Co/Al and Ni/Co/Al were synthesized for the first time by the urea hydrolysis method. The experimental conditions promoted aluminum rich and crystalline materials. The formation of LDHs was investigated by powder X-ray diffraction (XRD), chemical analysis, solid state nuclear magnetic resonance with magic angle spinning ({sup 27}Al-MAS-NMR), simultaneous thermogravimetric/differential thermal analysis (TGA/DTA), FTIR spectroscopy, scanning electron microscopy (SEM), and N{sub 2} adsorption–desorption experiments. A single phase corresponding to LDH could be obtained in all the investigated compositions. Thermal calcination of these LDHs at 500 °C resulted in the formation of solid solutions in which Al{sup 3+} was dissolved. All the calcined materials have rock-salt like structures and high surface areas.

  20. Hydrothermal zeolitisation controlled by host-rock lithofacies in the Periadriatic (Oligocene) Smrekovec submarine composite stratovolcano, Slovenia

    Science.gov (United States)

    Kralj, Polona

    2016-05-01

    Hydrothermal zeolites (laumontite, yugawaralite, analcime, heulandite, clinoptilolite), prehnite and pumpellyite have been recognised in a succession of volcanic, autoclastic, pyroclastic, resedimented volcaniclastic and mixed siliciclastic-volcaniclastic deposits. In cone-building lithofacies association attaining 310 m, the alteration minerals commonly change within a single normally graded depositional unit or alternate in the section on a dm- to m-scale, according to the host-rock lithofacies. Fine-grained deposits rich in juvenile glassy pyroclasts are altered to heulandite and clinoptilolite or analcime, and laumontite widely occurs in coarse-grained host-rocks (lapilli tuff, hyaloclastite breccia, volcaniclastic breccia, hyaloclastites) and fracture systems. In near-vent lithofacies association attaining 420 m, prehnite-laumontite, laumontite-analcime, and laumontite-heulandite-clinoptilolite zones developed as a result of superimposed thermal regime generated by the emplacement of an over 200 m thick sill. The recognised dependence of alteration on porosity, permeability and fracturing of the host-rock is closely related to hydrological conditions in the stratovolcano-hosted hydrothermal system with convective-advective flow regime. After separation of steam and gases from convecting hydrothermal fluids, denser liquids outflowed intermittently, preferentially through steeply inclined (20-30°) high-permeability layers in the stratovolcano edifice. In low-permeability layers the flow was slow and thermal conditions were mainly attained by conduction. Zeolites developed only in coarse- and fine-grained vitroclastic tuffs, presumably by the dissolution of volcanic glass. The interstratified siliciclastic siltstones, tuffites and resedimented deposits with low content of glassy particles are devoid of zeolites and indicate compositional constraint on zeolitisation. Lava flows, cooling in a submarine environment and undergoing disintegration and mingling with

  1. Hydrothermal synthesis and photocatalytic activities of Bi{sub 4}Ti{sub 3}O{sub 12}/SrTiO{sub 3} composite micro-platelets

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Wei, E-mail: zhaowei2004@tsinghua.org.cn; Wang, Hongxing; Feng, Xiangning; Jiang, Wangyang; Zhao, Dan; Li, Jiyuan

    2015-10-15

    Highlights: • Bi{sub 4}Ti{sub 3}O{sub 12}/SrTiO{sub 3} composite was fabricated by combining hydrothermal reaction and molten salt method. • Bi{sub 4}Ti{sub 3}O{sub 12}/SrTiO{sub 3} exhibits higher photocatalytic activity than pure Bi{sub 4}Ti{sub 3}O{sub 12}. • The absorption light of Bi{sub 4}Ti{sub 3}O{sub 12}/SrTiO{sub 3} has been broadened to visible light. - Abstract: In this study, Bi{sub 4}Ti{sub 3}O{sub 12}/SrTiO{sub 3} micro-platelets were successfully synthesized by using hydrothermal and molten salt methods, and the morphology and photocatalytic degradation performance of Bi{sub 4}Ti{sub 3}O{sub 12}/SrTiO{sub 3} was characterized. The results indicated a much higher degradation rate of methylene blue and methylene orange, reaching more than 90% and 65%, respectively, within 3 h under visible-light irradiation. Compared with pure Bi{sub 4}Ti{sub 3}O{sub 12}, the photocatalytic activity of Bi{sub 4}Ti{sub 3}O{sub 12}/SrTiO{sub 3} was significantly better, due to the micron–submicron heterojunction with SrTiO{sub 3} reducing the band gap of Bi{sub 4}Ti{sub 3}O{sub 12}. In addition, the perovskite structure layer facilitates the mobility of the photogenerated carriers and hampers their recombination, which were affected the photocatalytic properties.

  2. Controlled retting of hemp fibres: Effect of hydrothermal pre-treatmen tand enzymatic retting on the mechanical properties of unidirectiona lhemp/epoxy composites

    DEFF Research Database (Denmark)

    Liu, Ming; Silva, Diogo Alexandre Santos; Fernando, Dinesh

    2016-01-01

    The objective of this work was to investigate the use of hydrothermal pre-treatment and enzymatic retting to remove non-cellulosic compounds and thus improve the mechanical properties of hemp fibre/epoxy composites. Hydrothermal pre-treatment at 100 kPa and 121 °C combined with enzymatic retting...... produced fibres with the highest ultimate tensile strength (UTS) of 780 MPa. Compared to untreated fibres, this combined treatment exhibited a positive effect on the mechanical properties of hemp fibre/epoxy composites, resulting in high quality composites with low porosity factor (αpf) of 0.08.Traditional...

  3. Structural changes during synthesizing of nanostructured W-20 wt% Cu composite powder by mechanical alloying

    Energy Technology Data Exchange (ETDEWEB)

    Maneshian, M.H. [Department of Materials Science and Engineering, Sharif University of Technology, P.O. Box 11365-9466, Azadi Avenue, 14588 Tehran (Iran, Islamic Republic of); Simchi, A. [Department of Materials Science and Engineering, Sharif University of Technology, P.O. Box 11365-9466, Azadi Avenue, 14588 Tehran (Iran, Islamic Republic of) and Institute for Nanoscience and Nanotechnology, Sharif University of Technology, P.O. Box 11365-9466, Azadi Avenue, 14588 Tehran (Iran, Islamic Republic of)]. E-mail: simchi@sharif.edu; Hesabi, Z. Razavi [Department of Materials Science and Engineering, Sharif University of Technology, P.O. Box 11365-9466, Azadi Avenue, 14588 Tehran (Iran, Islamic Republic of)

    2007-02-15

    Nanostructured W-20 wt% Cu composite powder was synthesized by mechanical alloying (MA) in an Attritor ball mill. The morphological changes and structural evolution of the composite powder during MA was studied by employing scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive X-ray (EDX), laser particle size analyzer (LPS), inductively coupled plasma (ICP) spectrometry, atomic absorption spectrophotometery (AAS), and the bulk powder density measurement. The results were compared with those obtained from attrition milling of monolithic W and Cu powders processed at the same condition. Whereas the milling mechanism of the monolithic powders follow the ductile (for Cu) and semi-brittle (for W) systems, the W/Cu powder mixture exhibits different behavior. At the early stage of milling, the copper particles are fragmented and incorporated into the W matrix, resulting in the formation of W/Cu composite with laminar structure. With increasing milling time and due to continuous fracturing, the laminar structure is refined and a homogenous distribution of fine Cu particles (0.3-0.6 {mu}m) in the W matrix is formed. The analysis of XRD patterns indicated that the composite powder composes of nanostructured grains with the size of 49 nm for Cu and 23 nm for W. A faster grain refinement in the composite powder compared to the monolithic particles was noticed. The XRD peak intensity also revealed that partial mutual solubility of the constituent elements ({approx}4-7 at% for Cu in W and {approx}2-3 at% for W in Cu) was induced by prolonged mechanical milling.

  4. Electroless nickel plating of arc discharge synthesized carbon nanotubes for metal matrix composites

    Science.gov (United States)

    Jagannatham, M.; Sankaran, S.; Prathap, Haridoss

    2015-01-01

    Electroless nickel (EN) plating was performed on arc discharge synthesized multiwalled carbon nanotubes for various deposition times. X-ray diffraction (XRD), Transmission electron microscopy (TEM), and Raman spectroscopy characterization techniques are used to identify the presence of nickel deposition on the carbon nanotubes (CNTs) and the degree of graphitization. The results indicate that impurities are less in the purified CNTs as compared to raw carbon soot. Increasing deposition time up to 60 min increases uniform deposition of nickel throughout the length of the CNTs. However, for deposition time longer than 60 min, nickel particles are seen separated from the surface of the CNTs. Uniformly coated nickel CNTs throughout their length are potential candidates for reinforcements in composite materials. Magnetic properties of the nickel coated CNTs, with deposition time of 30 and 60 min were also evaluated. The magnetic saturation of nickel coated CNTs with deposition time of 30 min is less compared to nickel coated CNTs with deposition time of 60 min.

  5. Influence of Phase Composition on Sintered Microstructure of Combustion Synthesized Oxides

    Directory of Open Access Journals (Sweden)

    Ibram Ganesh

    2007-01-01

    Full Text Available The effects of powders synthesis methods (urea-combustion synthesis (CS and conventional solid-state (SS reaction on the sintering ability, microstructural features, and mechanical properties of Al2O3, MgAl2O4 spinel, and 20 wt.% ZrO2–MgAl2O4 upon sintering at 1625C∘ were investigated. X-ray diffraction (XRD, scanning electron microscopy (SEM, relative density (RD, apparent porosity and water absorption capacity, hardness, fracture toughness, and three-point bend test studies revealed the superior sintering ability of CS ZrO2-MgAl2O4 composite powder as compared with one prepared by SS reaction. In contrast, single-phase powders obtained by SS reaction exhibit superior sintering ability over CS synthesized ones. The reasons for differences observed are discussed along this paper.

  6. Lake-floor sediment texture and composition of a hydrothermally-active, volcanic lake, Lake Rotomahana

    Science.gov (United States)

    Pittari, A.; Muir, S. L.; Hendy, C. H.

    2016-03-01

    Young volcanic lakes undergo a transition from rapid, post-eruptive accumulation of volcaniclastic sediment to slower pelagic settling under stable lake conditions, and may also be influenced by sublacustrine hydrothermal systems. Lake Rotomahana is a young (129 year-old), hydrothermally-active, volcanic lake formed after the 1886 Tarawera eruption, and provides a unique insight into the early evolution of volcanic lake systems. Lake-bottom sediment cores, 20-46 cm in length, were taken along a transect across the lake and characterised with respect to stratigraphy, facies characteristics (i.e., grain size, componentry) and pore water silica concentrations. The sediments generally comprise two widespread facies: (i) a lower facies of light grey to grey, very fine lacustrine silt derived from the unconsolidated pyroclastic deposits that mantled the catchment area immediately after the eruption, which were rapidly reworked and redeposited into the lake basin; and (ii) an upper facies of dark, fine-sandy diatomaceous silt, that settled from the pelagic zone of the physically stable lake. Adjacent to sublacustrine hydrothermal vents, the upper dark facies is absent, and the upper part of the light grey to grey silt is replaced by a third localised facies comprised of hydrothermally altered pale yellow to yellowish brown, laminated silt with surface iron-rich encrustations. Microspheres, which are thought to be composed of amorphous silica, although some may be halloysite, have precipitated from pore water onto sediment grains, and are associated with a decrease in pore water silicon concentration. Lake Rotomahana is an example of a recently-stabilised volcanic lake, with respect to sedimentation, that shows signs of early sediment silicification in the presence of hydrothermal activity.

  7. Electroless nickel plating of arc discharge synthesized carbon nanotubes for metal matrix composites

    Energy Technology Data Exchange (ETDEWEB)

    Jagannatham, M.; Sankaran, S.; Prathap, Haridoss, E-mail: prathap@iitm.ac.in

    2015-01-01

    Highlights: • Electroless Ni coatings have been performed on CNTs for various deposition times. • The deposition of nickel increased with increase in deposition time. • A deposition time of 60 min has been optimum for uniform coating of Ni on CNTs. • The CNTs with uniform coating of Ni are potential for reinforcements in composites. • Electroless nickel coatings are determined to be super paramagnetic behavior. - Abstract: Electroless nickel (EN) plating was performed on arc discharge synthesized multiwalled carbon nanotubes for various deposition times. X-ray diffraction (XRD), Transmission electron microscopy (TEM), and Raman spectroscopy characterization techniques are used to identify the presence of nickel deposition on the carbon nanotubes (CNTs) and the degree of graphitization. The results indicate that impurities are less in the purified CNTs as compared to raw carbon soot. Increasing deposition time up to 60 min increases uniform deposition of nickel throughout the length of the CNTs. However, for deposition time longer than 60 min, nickel particles are seen separated from the surface of the CNTs. Uniformly coated nickel CNTs throughout their length are potential candidates for reinforcements in composite materials. Magnetic properties of the nickel coated CNTs, with deposition time of 30 and 60 min were also evaluated. The magnetic saturation of nickel coated CNTs with deposition time of 30 min is less compared to nickel coated CNTs with deposition time of 60 min.

  8. Improved waste water treatment by bio-synthesized Graphene Sand Composite.

    Science.gov (United States)

    Poornima Parvathi, V; Umadevi, M; Bhaviya Raj, R

    2015-10-01

    The photocatalytic and antibacterial properties of graphene biosynthesized from sugar and anchored on sand particles has been focused here. The morphology and composition of the synthesized Graphene Sand Composite (GSC) was investigated by means of X-ray powder diffraction (XRD), Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Spectroscopy (EDAX), Fourier Transform Infra-red Spectroscopy (FTIR) and UV-Visible spectroscopy. SEM images show wrinkly edges. This is characteristic of graphenic morphology. Three types of waste water samples namely, textile waste (TW), sugarcane industrial waste water (SW) and domestic waste water from a local purification center at Kodaikanal (KWW) were collected and treated. Adsorption experiments showed effective removal of impurities at 0.2 g of GSC. Photocatalytic activity was analyzed under visible and ultraviolet irradiation. The rate constant for TW increased to 0.0032/min for visible light irradiation from 0.0029/min under UV irradiation. SW showed similar improved activity with rate constant as 0.0023/min in visible irradiation compared to 0.0016/min under UV irradiation. For KWW enhanced activity was seen only in visible light irradiation with rate constant 0.0025/min. GSC showed an inhibition zone of 20 mm against the bacterium Escherichia coli. Results suggest development of economic and effective waste water management systems. Copyright © 2015 Elsevier Ltd. All rights reserved.

  9. Optical properties of nanometre AgI silica composite synthesized by a simple quenching method

    Science.gov (United States)

    He, Haiping; Wang, Yuxia; Zou, Youming

    2003-07-01

    Optical absorption and room temperature photoluminescence (PL) properties of nanometre AgI-silica composite synthesized by a simple heating-quenching method were investigated. The absorption of quenched AgI-silica was enhanced markedly. Three absorption bands at 440 (2.8 eV), 260 (4.8 eV) and 220 nm (5.6 eV) were observed. The excitonic absorption of AgI showed a red shift of ~0.11 eV, in contrast to the usually observed blue shift in AgI nanocrystals. Besides two UV emissions from a non-bridging hole centre and E' centre defects formed in silica, the composite exhibited two PL emissions at 2.62 and 2.40 eV. The 2.62 eV PL was ascribed to donor-acceptor recombination of AgI, while the 2.40 eV one may correlate with energy levels induced by the interaction between silica and AgI. The role of silica in improving the PL for nanometre AgI is discussed.

  10. Evaluation of Synthesized Nanohydroxyapatite-Nanocellulose Composites as Biocompatible Scaffolds for Applications in Bone Tissue Engineering

    Directory of Open Access Journals (Sweden)

    Claudia S. Herdocia-Lluberes

    2015-01-01

    Full Text Available Basic calcium phosphate (BCP crystals have been associated with many diseases due to their activation of signaling pathways that lead to their mineralization and deposition in intra-articular and periarticular locations in the bones. In this study, hydroxyapatite (HAp has been placed in a polysaccharide network as a strategy to minimize this deposition. This research consisted of the evaluation of varying proportions of the polysaccharide network, cellulose nanocrystals (CNCs, and HAp synthesized via a simple sol-gel method. The resulting biocompatible composites were extensively characterized by means of thermogravimetric analysis (TGA, powder X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FT-IR, dynamic light scattering (DLS, zeta potential, and scanning electron microscopy (SEM. It was found that an nHAp = CNC ratio presented greater homogeneity in the size and distribution of the nanoparticles without compromising the crystalline structure. Also, incorporation of bone morphogenetic protein 2 (BMP-2 was performed to evaluate the effects that this interaction would have in the constructs. Finally, the osteoblast cell (hFOB 1.19 viability assay was executed and it showed that all of the materials promoted greater cell proliferation while the nHAp > CNC proportion with the inclusion of the BMP-2 protein was the best composite for the purpose of this study.

  11. Diffuse-flow hydrothermal field in an oceanic fracture zone setting, Northeast Pacific: Deposit composition

    Science.gov (United States)

    Hein, J.R.; Koski, R.A.; Embley, R.W.; Reid, J.; Chang, S.-W.

    1999-01-01

    This is the first reported occurrence of an active hydrothermal field in an oceanic fracture zone setting. The hydrothermal field occurs in a pull-apart basin within the Blanco Fracture Zone (BFZ), which has four distinct mineral deposit types: (1) barite mounds and chimneys, (2) barite stockwork breccia, (3) silica-barite beds, and (4) silica, barite, and Fe-Mn oxyhydroxide in sediments. All deposit types contain minor amounts of sulfides. In barite stockwork, silica-barite beds, and mineralized sediment, Ba, Ph, Ag, S, Au, Zn, Cu, Hg, TI, As, Mo, Sb, U, Cd, and Cu are enriched relative to unmineralized rocks and sediments of the BFZ. Fe and Mn are not enriched in the barite stockwork or silica-barite beds, but along with P, Co, and Mg are enriched in the mineralized sediments. Silver contents in deposits of the hydrothermal field range up to 86 ppm, gold to 0.7 ppm, zinc to 3.2%, copper to 0.8%, and barium to 22%. Mineralization occurred by diffuse, low to intermediate temperature (mostly Metallurgy and Petroleum. All rights reserved.

  12. Nanocrystalline nickel ferrite particles synthesized by non-hydrolytic sol-gel method and their composite with biodegradable polymer.

    Science.gov (United States)

    Yin, H; Casey, P S; Chow, G M

    2012-11-01

    Targeted drug delivery has been one of the most important biomedical applications for magnetic particles. Such applications require magnetic particles to have functionalized surfaces/surface coatings that facilitate their incorporation into a polymer matrix to produce a polymer composite. In this paper, nanocrystalline nickel ferrite particles with an oleic acid surface coating were synthesized using a non-hydrolytic sol-gel method and incorporated into a biodegradable polymer matrix, poly(D,L-lactide) PLA prepared using a double emulsion method. As-synthesized nickel ferrite particles had a multi-crystalline structure with chemically adsorbed oleic acid on their surface. After forming the PLA composite, nickel ferrite particles were encapsulated in PLA microspheres. At low nickel ferrite concentrations, composites showed very similar surface charges to that of PLA. The composites were magnetically responsive and increasing the nickel ferrite concentration was found to increase magnetization of the composite.

  13. Mercury isotopic composition of hydrothermal systems in the Yellowstone Plateau volcanic field and Guaymas Basin sea-floor rift

    Science.gov (United States)

    Sherman, L.S.; Blum, J.D.; Nordstrom, D.K.; McCleskey, R.B.; Barkay, T.; Vetriani, C.

    2009-01-01

    To characterize mercury (Hg) isotopes and isotopic fractionation in hydrothermal systems we analyzed fluid and precipitate samples from hot springs in the Yellowstone Plateau volcanic field and vent chimney samples from the Guaymas Basin sea-floor rift. These samples provide an initial indication of the variability in Hg isotopic composition among marine and continental hydrothermal systems that are controlled predominantly by mantle-derived magmas. Fluid samples from Ojo Caliente hot spring in Yellowstone range in δ202Hg from - 1.02‰ to 0.58‰ (± 0.11‰, 2SD) and solid precipitate samples from Guaymas Basin range in δ202Hg from - 0.37‰ to - 0.01‰ (± 0.14‰, 2SD). Fluid samples from Ojo Caliente display mass-dependent fractionation (MDF) of Hg from the vent (δ202Hg = 0.10‰ ± 0.11‰, 2SD) to the end of the outflow channel (&delta202Hg = 0.58‰ ± 0.11‰, 2SD) in conjunction with a decrease in Hg concentration from 46.6pg/g to 20.0pg/g. Although a small amount of Hg is lost from the fluids due to co-precipitation with siliceous sinter, we infer that the majority of the observed MDF and Hg loss from waters in Ojo Caliente is due to volatilization of Hg0(aq) to Hg0(g) and the preferential loss of Hg with a lower δ202Hg value to the atmosphere. A small amount of mass-independent fractionation (MIF) was observed in all samples from Ojo Caliente (Δ199Hg = 0.13‰ ±1 0.06‰, 2SD) but no significant MIF was measured in the sea-floor rift samples from Guaymas Basin. This study demonstrates that several different hydrothermal processes fractionate Hg isotopes and that Hg isotopes may be used to better understand these processes.

  14. Upconversion Luminescence Properties of Ho3+, Tm3+, Yb3+ Co-Doped Nanocrystal NaYF4 Synthesized by Hydrothermal Method

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Nanocrystal of upconversion (UC) phosphor Ho3+, Tm3+, and Yb3+ co-doped NaYF4 was prepared by the hydrothermal method in the presence of the complexing agent EDTA. Under 980 nm diode laser excitation, the impact of different concentrations of Ho3+ ion on the UC luminescence intensity was discussed. The law of luminescence intensity versus pump power shows that the 474 nm blue emission, 538 nm green emission, and 642 nm red emission are all due to the two-photon process, while the 450 nm blue emission is a three-photon process. The UC mechanism and processes were also analyzed. The sample was characterized by transmission electron microscopy (TEM) and X-ray diffraction (XRD). The result shows that Ho3+, Tm3+, and Yb3+ co-doped NaYF4 prepared by the hydrothermal method exhibits a hexagonal nanocrystal.

  15. Obtaining zeolite Y synthesized by hydrothermal treatment assisted by microwave; Obtencao de zeolita Y sintetizada atraves de tratamento hidrotermico assistido por microondas

    Energy Technology Data Exchange (ETDEWEB)

    Simoes, A.N.; Simoes, V.N.; Neiva, L.S.; Rodrigues, M.G.F.; Gama, L., E-mail: Alluskynha@hotmail.com [Universidade Federal de Campina Grande (UFCG), PB (Brazil); Oliveira, J. B.L. [Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN (Brazil). Departamento de Quimica

    2011-07-01

    n search of new catalysts several man-made structures have been developed. The use of zeolites in catalysis is applied due to its ability to associate activity, selectivity and stability, the main conditions to have an effective catalyst. Thus, studies have been done on the hydrothermal synthesis of zeolites by microwave assisted, since the use of microwave radiation offers several advantages over conventional heating. In this context, this work aims to synthesis and characterization of zeolite Y via hydrothermal treatment in a microwave oven. The sample obtained was characterized by XRD, BET and SEM. XRD results showed the formation of zeolite Y in just 60 minutes. The sample showed high value of surface area, the latter being of 476.2 m² / g. The particles are agglomerated, but with a narrow distribution of size. (author)

  16. A novel hydrothermal approach for synthesizing α-Fe{sub 2}O{sub 3}, γ-Fe{sub 2}O{sub 3} and Fe{sub 3}O{sub 4} mesoporous magnetic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Jayanthi, S. Amala [Department of Physics, Government Arts College (Autonomous), Nandanam, Chennai, 600 035 (India); Nathan, D. Muthu Gnana Theresa; Jayashainy, J. [Department of Physics, Loyola College (Autonomous), Chennai, 600 034 (India); Sagayaraj, P., E-mail: psagayaraj@hotmail.com [Department of Physics, Loyola College (Autonomous), Chennai, 600 034 (India)

    2015-07-15

    A novel method to synthesize the three phases of iron oxide nanoparticles (hematite, maghemite and magnetite) using the same non-toxic inorganic precursors via a water–organic interface under the low temperature hydrothermal conditions is reported. The synthesized particles are characterized by Powder X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM) and Transmission Electron Microscopy (TEM). The Brunauer–Emmett–Teller (BET) results reveal the mesoporous nature of the particles. The magnetic properties of the nanoparticles are studied by Vibrating Sample Magnetometer (VSM) at various low temperatures and also at room temperature. The XRD peaks corresponding to each sample clearly depict the presence of the respective phase of the as-prepared magnetic nanoparticles. The nanoparticles of maghemite and magnetite have saturation magnetization of 58.56 and 40.30 emu/g respectively at room temperature, whereas the particles of hematite possess very low saturation magnetization value of 1.89 emu/g. Further, the magnetization is studied at four different temperatures and the zero field cooled (ZFC) and field cooled (FC) magnetization are reported. - Graphical abstract: Display Omitted - Highlights: • Hematite, maghemite and magnetite are obtained under hydrothermal synthesis. • α-Fe{sub 2}O{sub 3}, γ-Fe{sub 2}O{sub 3} and Fe{sub 3}O{sub 4} prepared are mesoporous and nearly monodisperse. • Near superparamagnetism is observed at room temperature for maghemite and magnetite.

  17. A reconnaissance of the Cu isotopic compositions of hydrothermal vein-type cop-per deposit, Jinman, Yunnan,China

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The Jinman deposit is a low-temperature hydrothermal vein-type copper deposit, which occurs along faults and fractures within Middle Jurassic sandstone and mudstone units of the Lanping-Simao Mesozoic-Cenozoic basin of Yunnan Province. In this note, we report for the first time the Cu isotopic compositions of Cu-sulfides from the Jinman deposit. The data show large variations and low 65Cu values of 3.70‰ to +0.30‰, which are in sharp contrast to the 65Cu values of high-temperature magmatic-hydrothermal copper deposits (0.62‰ to +0.40‰) and the modern ocean-floor massive sulfide deposits (0.48‰ to +1.15‰). It is suggested that the Cu isotope fractionation at Jinman is affected mainly by the following factors, i.e. a low temperature of ore formation (150-286℃); a sedimentary source for ore materials; various stages of ore deposition; and involvement of organic matter in the ore-forming processes.

  18. Chemical, isotopic, and dissolved gas compositions of the hydrothermal system in Twin Falls and Jerome counties, Idaho

    Science.gov (United States)

    Mariner, R.H.; Young, H.W.; Evans, ans; Parliman, D.J.

    1991-01-01

    The chemical, isotopic, and gas compositions of the hydrothermal system in Twin Falls and Jerome counties, Idaho, change systematically as the water moves northward from the Idaho-Nevada boundary toward the Snake River. Sodium, chloride, fluoride, alkalinity, dissolved helium, and carbon-13 increase as calcium and carbon-14 decrease. Water-rock reactions may result in dissolution of plagioclase or volcanic glass and calcite, followed by precipitation of zeolites and clays. On the basis of carbon-14 age dating, apparent water ages range from 2,000 to more than 26,000 years; most apparent ages range from about 4,000 to 10,000 years. The older waters, north of the Snake River, are isotopically depleted in deuterium and are enriched in chloride relative to waters to the south. Thermal waters flowing northward beneath the Snake River may join a westward flow of older thermal water slightly north of the river. The direction of flow in the hydrothermal system seems to parallel the surface drainage.

  19. 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...

  20. Preparation of a Titania/X-Zeolite/Porous Glass Composite Photocatalyst Using Hydrothermal and Drop Coating Processes

    Directory of Open Access Journals (Sweden)

    Atsuo Yasumori

    2015-01-01

    Full Text Available Combinations of TiO2 photocatalysts and various adsorbents have been widely studied for the adsorption and photocatalytic decomposition of gaseous pollutants such as volatile organic compounds (VOCs. Herein, a TiO2-zeolite-porous glass composite was prepared using melt-quenching and partial sintering, hydrothermal treatment, and drop coating for preparation of the porous glass support and X-zeolite and their combination with TiO2, respectively. The obtained composite comprised anatase phase TiO2, X-zeolite, and the porous glass support, which were combined at the micro to nanometer scales. The composite had a relatively high specific surface area of approximately 25 m2/g and exhibited a good adsorption capacity for 2-propanol. These data indicated that utilization of this particular phase-separated glass as the support was appropriate for the formation of the bulk photocatalyst-adsorbent composite. Importantly, the photocatalytic decomposition of adsorbed 2-propanol proceeded under UV light irradiation. The 2-propanol was oxidized to acetone and then trapped by the X-zeolite rather than being released to the atmosphere. Consequently, it was demonstrated that the micrometer-scaled combination of TiO2 and zeolite in the bulk form is very useful for achieving both the removal of gaseous organic pollutants and decreasing the emission of harmful intermediates.

  1. Composition tunable cobalt–nickel and cobalt–iron alloy nanoparticles below 10 nm synthesized using acetonated cobalt carbonyl

    NARCIS (Netherlands)

    van Schooneveld, Matti M.|info:eu-repo/dai/nl/315032863; Campos-Cuerva, Carlos; Pet, Jeroen; Meeldijk, Johannes D.|info:eu-repo/dai/nl/323921647; van Rijssel, Jos; Meijerink, Andries; Erne, Ben H.|info:eu-repo/dai/nl/141937378; de Groot, Frank M. F.|info:eu-repo/dai/nl/08747610X

    A general organometallic route has been developed to synthesize CoxNi1-x and CoxFe1-x alloy nanoparticles with a fully tunable composition and a size of 4–10 nm with high yield. In contrast to previously reported synthesis methods using dicobalt octacarbonyl (Co2(CO)8), here the cobalt–cobalt bond

  2. Composition tunable cobalt–nickel and cobalt–iron alloy nanoparticles below 10 nm synthesized using acetonated cobalt carbonyl

    NARCIS (Netherlands)

    van Schooneveld, Matti M.; Campos-Cuerva, Carlos; Pet, Jeroen; Meeldijk, Johannes D.; van Rijssel, Jos; Meijerink, Andries; Erne, Ben H.; de Groot, Frank M. F.

    2012-01-01

    A general organometallic route has been developed to synthesize CoxNi1-x and CoxFe1-x alloy nanoparticles with a fully tunable composition and a size of 4–10 nm with high yield. In contrast to previously reported synthesis methods using dicobalt octacarbonyl (Co2(CO)8), here the cobalt–cobalt bond i

  3. Carbon/Clay nanostructured composite obtained by hydrothermal method; Compositos nanoestruturados carbono/argila obtidos por metodo hidotermico

    Energy Technology Data Exchange (ETDEWEB)

    Barin, G.B.; Bispo, T.S.; Gimenez, I.F.; Barreto, L.S., E-mail: gabriela.borin@gmail.co [Universidade Federal de Sergipe (UFS), Aracaju, SE (Brazil). Programa de Pos-Graduacao em Ciencia e Engenharia de Materiais; Souza Filho, A.G. [Universidade Federal do Ceara (UFC), Fortaleza, CE (Brazil). Dept. de Fisica

    2010-07-01

    The development of strategies for converting biomass into useful materials, more efficient energy carrier and / or hydrogen storage is shown a key issue for the present and future. Carbon nanostructure can be obtained by severe processing techniques such as arc discharge, chemical deposition and catalyzed pyrolysis of organic compounds. In this study we used hydrothermal methods for obtaining nanostructured composites of carbon / clay. To this end, we used coir dust and special clays. The samples were characterized by infrared spectroscopy, X-ray diffraction and Raman. The presence of the D band at 1350 cm{sup -1} in the Raman spectrum shows the formation of amorphous carbon with particle size of about 8.85 nm. (author)

  4. Carbon/Clay nanostructured composite obtained by hydrothermal method; Compositos nanoestruturados carbono/argila obtidos por metodo hidotermico

    Energy Technology Data Exchange (ETDEWEB)

    Barin, G.B.; Bispo, T.S.; Gimenez, I.F.; Barreto, L.S., E-mail: gabriela.borin@gmail.co [Universidade Federal de Sergipe (UFS), Aracaju, SE (Brazil). Programa de Pos-Graduacao em Ciencia e Engenharia de Materiais; Souza Filho, A.G. [Universidade Federal do Ceara (UFC), Fortaleza, CE (Brazil). Dept. de Fisica

    2010-07-01

    The development of strategies for converting biomass into useful materials, more efficient energy carrier and / or hydrogen storage is shown a key issue for the present and future. Carbon nanostructure can be obtained by severe processing techniques such as arc discharge, chemical deposition and catalyzed pyrolysis of organic compounds. In this study we used hydrothermal methods for obtaining nanostructured composites of carbon / clay. To this end, we used coir dust and special clays. The samples were characterized by infrared spectroscopy, X-ray diffraction and Raman. The presence of the D band at 1350 cm{sup -1} in the Raman spectrum shows the formation of amorphous carbon with particle size of about 8.85 nm. (author)

  5. 2D laminated cylinder-like BiFeO3 composites: Hydrothermal preparation, formation mechanism, and photocatalytic properties

    Science.gov (United States)

    Gao, Xiaoming; Dai, Yuan; Fu, Feng; Hua, Xiufu

    2016-12-01

    BiFeO3 perovskite with 2D laminated cylinder-like structure was prepared via a facile one-pot hydrothermal method, whose morphologies and optical properties was characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersion spectrum (EDS), and UV-Visible diffuse reflectance spectroscopy (UV-Vis DRS). The photocatalytic properties of the as-prepared BiFeO3 composites were evaluated according to degrading Rhodamine B (RhB) and desulfurization under visible light irradiation, with excellent photocatalytic degradation and desulfurization activity found. Moreover, the mechanism study of active free radicals in photocatalytic activity indicates that the h+ radical in holes was mainly responsible for synergistic catalytic efficacy in photocatalytic degradation.

  6. Composition-volume changes during hydrothermal alteration of andesite at Buttercup Hill, Noranda District, Quebec

    Science.gov (United States)

    Lesher, C. M.; Gibson, H. L.; Campbell, I. H.

    1986-12-01

    Hydrothermally altered andesites in the upper member of the Amulet formation at Buttercup Hill, Noranda, Quebec represent part of the aquifer and cap of a self-sealing geothermal system that focussed the discharge of hydrothermal fluids during the formation of massive Cu-Zn sulfide deposits. Five alteration facies are recognized pervasive greenschist faciés regional metamorphism (least-altered andesite) epidotization-silicification albitization-silicification chloritization sericitization-silicification. Alteration is localized on permeable zones such as amygdules, fractures, flow tops, discordant breccia dikes, and conformable breccia horizons. Epidotized-silicified andesite is enriched in Ca-Sr-Eu and depleted in Mg and first transition series metals (FTSM) relative to least-altered andesite. Albitized-silicified andesite is significantly enriched in Na and depleted in most FTSM relative to least-altered andesite. The abundances and inter-element ratios of the rare-earth elements (REE) and most high field-strength elements (HFS: Y, Zr, Th, U, Hf, Ta) are similar in least-altered, epidotized-silicified and albitized-silicified andesites. The most silicified andesites are strongly enriched in Na-Si, strongly depleted in Mg and divalent FTSM and slightly but systematically depleted in REE and most HFS elements. Serialized andesites were previously silicified; they are very strongly enriched in K-Rb-Cs-Ba, very strongly depleted in Na-Ca-Sr-Eu and slightly depleted in light REE relative to silicified andesite. Chloritized andesitic rocks exhibit heavy REE and HFS element ratios similar to those of leastaltered andesite, but are relatively strongly enriched in Mg and divalent FTSM, strongly depleted in Si and large ion lithophile (LIL) elements and slightly depleted in light REE. The coupled behavior of the heavy REE and most HFS elements during epidotization, albitization, silicification, chloritization and serialization suggests that they were inert during

  7. Electrical and optical study of ultrasonic-assisted hydrothermal synthesized Ga doped ZnO nanorods for polymer solar cell application

    Science.gov (United States)

    Ahmadi, M.; Rashidi Dafeh, S.

    2016-08-01

    Ga doped ZnO nanorods with homogeneous morphology grown by ultrasonic-assisted hydrothermal method on ITO substrate. The effect of hydrothermal growth times 30, 60, 90 and 120 min on the characteristics of ZnO nanorods was examined. The samples were analyzed by X-ray diffraction, scanning electron microscopy, UV-Vis spectrometer and conductivity measurement. With the optimization of the growth times (60 min), we employed Ga doped ZnO nanorods with diverse dopant concentration in fabrication of polymer solar cell. By comparing the effect of Ga doped ZnO thin films with various dopant ratio (0, 0.5, 1.0 and 2 %) on the performance of Ga doped ZnO thin films, 0.5 % Ga doped ZnO was found as the most effective doping level among the selected doping concentrations. Also using 0.5 % Ga doped ZnO thin film, Jsc of 7.54 mA/cm2, Voc of 0.541 V, and fill factor of 64.81 % were achieved, which led to power conversion efficiency of 2.64 %.

  8. Composition and structure of Pt chloride complexes in hydrothermal solutions, according to X-ray absorption spectroscopy

    Science.gov (United States)

    Tagirov, B. R.; Trigub, A. L.; Selivanov, P. V.; Koroleva, L. A.

    2017-03-01

    The local atomic environment of Pt in chloride solutions is studied at 25 and 300-350°C via X-ray absorption spectroscopy. A comparison of the Pt L 3-edge XANES spectra for aqueous chloride solutions and reference compounds (K2PtCl4 and K2PtCl6) shows that platinum is in oxidation state +2 at all temperatures, and the complex composition remains unchanged in the experimental range of temperatures (25-350°C) and solution compositions ( m(Cltot) > 0.4 mol kg-1 of H2O). Based on EXAFS spectral analysis, the composition of the complex being dominant in chloride solutions is found to be PtCl4 2- with interatomic Pt-Cl distances of 2.31 ± 0.01 Å, regardless of the temperature. It is concluded that the local environments of Pt and Pd in hydrothermal solutions are similar, and the main form of transfer for these metals is a square-planar complex with four Cl ligands and identical interatomic distances.

  9. Nanoemulsion drug delivery by ketene based polyester synthesized using electron rich carbon/silica composite surface.

    Science.gov (United States)

    Swarnalatha, S; Selvi, P K; Ganesh Kumar, A; Sekaran, G

    2008-09-01

    A new carrier matrix for nanoemulsion drug delivery was synthesized from glycine as the raw material, using mesoporous/microporous electron rich carbon-silica composite surface (MAC(800)). MAC(800) was prepared from rice husk in two-stage carbonization. The surface area, pore volume, and pore size distribution of MAC(800) were measured, using nitrogen adsorption isotherms at 77K. The unpaired electron density of MAC(800) was measured in electron spin resonance spectroscopy (ESR), using TEMPOL (4-hydroxy-2,2,6,6-tetramethyl piperidine-1-oxyl) as the reference spin probe. Glycine was converted into ketene at the surface of MAC(800), which further underwent radical polymerization to form a low molecular weight ketene polymer (LMKP) of ester structure. The structure and the properties of LMKP were confirmed through (13)C, (1)H and DEPT nuclear magnetic resonance (NMR) spectroscopy, attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) and size exclusion chromatography (SEC). The two hydrophilic drugs namely ciprofloxacin hydrochloride (CPH) and gentamicin sulphate (GS) were chosen for the nanoemulsion preparation and characterization. They were characterized for morphology, interaction of drugs with the polymer and their crystallinity, using HR-TEM, DSC and XRD, respectively. The encapsulation efficiency of the LMKP towards the drugs ciprofloxacin hydrochloride and gentamicin sulphate were 26% and 12%, respectively. The dissolution studies of the nanoemulsion were carried out for the pH 6.5, 7.4 and 8.0. The cytocompatibility studies were done for LMKP as well as nanoemulsion using Hep2 epithelial cells.

  10. High temperature creep behavior of in-situ synthesized MoSi2-30%SiC composite

    Institute of Scientific and Technical Information of China (English)

    傅晓伟; 杨王玥; 孙祖庆; 张来启; 朱静

    2002-01-01

    The compressive creep behavior at 1200~1400℃ of an in-situ synt hesized MoSi2-30%SiC (volume fraction) composite and a traditional PM MoSi2 -30%SiC (volume fraction) composite is investigated. The creep rate of the in -situ synthesized MoSi2-30%SiC (volume fraction) composite is about 10- 7s-1 under stress of 60~120MPa, and significantly lower than that made by PM method above 1300℃. The reason is that the interface be tween SiC particle and MoSi2 matrix in in-situ synthesized SiCp/MoSi2 is of direct atomic bonding without any amorphous glassy phase, such as SiO2 stru cture. Creep deformation occurs primarily by dislocation motion and the dislocat ions have Burgers vectors of the ty pe of 〈110〉 and 〈100〉.

  11. Enhanced photocatalytic degradation of methylene blue by ZnO-reduced graphene oxide composite synthesized via microwave-assisted reaction

    Energy Technology Data Exchange (ETDEWEB)

    Lv Tian [Engineering Research Center for Nanophotonics and Advanced Instrument, Ministry of Education, Department of Physics, East China Normal University, Shanghai, 200062 (China); Pan Likun, E-mail: lkpan@phy.ecnu.edu.cn [Engineering Research Center for Nanophotonics and Advanced Instrument, Ministry of Education, Department of Physics, East China Normal University, Shanghai, 200062 (China); Liu Xinjuan; Lu Ting; Zhu Guang; Sun Zhuo [Engineering Research Center for Nanophotonics and Advanced Instrument, Ministry of Education, Department of Physics, East China Normal University, Shanghai, 200062 (China)

    2011-10-13

    Highlights: > ZnO-reduced graphene oxide composite is synthesized via microwave assisted reaction. > The method allows a facile, safe and rapid reaction in aqueous media. > A high dye degradation efficiency is achieved under UV light irradiation. - Abstract: A quick and facile microwave-assisted reaction is used to synthesize ZnO-reduced graphene oxide (RGO) hybrid composites by reducing graphite oxide dispersion with zinc nitrate using a microwave synthesis system. Their photocatalytic performance in degradation of methylene blue is investigated and the results show that the RGO plays an important role in the enhancement of photocatalytic performance and the ZnO-RGO composite with 1.1 wt. % RGO achieves a maximum degradation efficiency of 88% in a neutral solution under UV light irradiation for 260 min as compared with pure ZnO (68%) due to the increased light absorption, the reduced charge recombination with the introduction of RGO.

  12. In situ hydrothermal synthesis of a novel hierarchically porous TS-1/modified-diatomite composite for methylene blue (MB) removal by the synergistic effect of adsorption and photocatalysis.

    Science.gov (United States)

    Yuan, Weiwei; Yuan, Peng; Liu, Dong; Yu, Wenbin; Laipan, Minwang; Deng, Liangliang; Chen, Fanrong

    2016-01-15

    Hierarchically porous TS-1/modified-diatomite composites with high removal efficiency for methylene blue (MB) were prepared via a facile in situ hydrothermal route. The surface charge state of the diatomite was modified to enhance the electrostatic interactions, followed by in situ hydrothermal coating with TS-1 nanoparticles. The zeolite loading amount in the composites could be adjusted by changing the hydrothermal time. The highest specific surface area and micropore volume of the obtained composites were 521.3m(2)/g and 0.254cm(3)/g, respectively, with an optimized zeolite loading amount of 96.8%. Based on the synergistic effect of efficient adsorption and photocatalysis resulting from the newly formed hierarchically porous structure and improved dispersion of TS-1 nanoparticles onto diatomite, the composites' removal efficiency for MB reached 99.1% after 2h of photocatalytic reaction, even higher than that observed using pure TS-1 nanoparticles. Moreover, the superior MB removal kinetics of the composites were well represented by a pseudo-first-order model, with a rate constant (5.28×10(-2)min(-1)) more than twice as high as that of pure TS-1 nanoparticles (2.43×10(-2)min(-1)). The significant dye removal performance of this novel TS-1/modified-diatomite composite indicates that it is a promising candidate for use in waste water treatment.

  13. Conversion of Induction Heating Deposited Monetite Coating to Hydroxyapatite Coating on Ht-C Composites by Hydrothermal Treatment in KOH Aqueous/ammonia Solution

    Science.gov (United States)

    Li, Dong-Mei; Xiong, Xin-Bo; Zeng, Xie-Rong; Zou, Chun-Li; Zou, Ji-Zhao

    Carbon/carbon composites with hydroxyapatite coatings are one of the attractive materials in the dental and orthopedic fields. In this study, hydrothermal treatment, in KOH aqueous and ammonia solutions, was used to convert an induction-heating-deposited monetite coating to an adherent HA coating on H2O2 treated C/C composites. The structure, morphology and chemical composition of the as-received HA coatings were characterized by XRD, FTIR, SEM and EDS. A scratch test was conducted to measure the adhesion of HA coatings to HT-C/C substrate. The results show that well-crystallized carbonate hydroxyapatite coatings could be achieved under the two reaction mediums. However, the as-obtained HA coatings after KOH hydrothermal treatment have higher crystallinity and Ca/P ratio than those after ammonia hydrothermal treatment, and reveal an average critical load of 29 N which is more than two times as high as that for HA coatings after ammonia hydrothermal treatment.

  14. Detailed paragenesis and Li-mica compositions as recorders of the magmatic-hydrothermal evolution of the Maoping W-Sn deposit (Jiangxi, China)

    Science.gov (United States)

    Legros, Hélène; Marignac, Christian; Mercadier, Julien; Cuney, Michel; Richard, Antonin; Wang, Ru-Cheng; Charles, Nicolas; Lespinasse, Marc-Yves

    2016-11-01

    Li-micas have been used as indicators of the evolution of granites. However, hydrothermal Li-micas are less documented. World-class W-Sn deposits associated with Early Yanshanian granites (South Jiangxi, China) show magmatic and hydrothermal Li-micas which could help unravelling the magmatic-hydrothermal evolution of rare metal deposits. Six types of Li-micas have been identified in the vein system of the Maoping W-Sn deposit through detailed petrography and EPMA and LA-ICP-MS analyses, by chronological order: (i) late-magmatic Li-micas in feldspar veins, associated with late crystallization of a peraluminous melt; (ii) hydrothermal Fe-Li micas (Fe-Li mica veins and selvages); (iii) hydrothermal Fe-Li micas in W-Sn veins; (iv) Fe-Li micas in later banded quartz veins; (v) Li-muscovite in the final stages; and finally (vi) micas associated with alteration at each stage. Based on oscillatory variations and trends in major elements composition, the chemical variations in Li-micas from the successive stages and in hydrothermal micas that crystallized in the veins are interpreted to reflect mixing between at least three fluids of possible magmatic, meteoric and metamorphic origins. The crystallization of zircons and REE minerals, combined with variations of major and trace element concentrations in the Li-micas, notably an enrichment of rare metals (W-Sn-Ta-Nb) in the Li-micas, implies emplacement of a hidden peralkaline REE-rich magma during the crystallization of the banded quartz veins, a source which was different to the pre-existing peraluminous granites. The possible involvement of both peraluminous and peralkaline intrusives suggests the existence of polyphase magmatic-hydrothermal systems in the Maoping deposit, during the Yanshanian event (190-80 Ma).

  15. Microwave Hydrothermal Synthesis PZT of Nanometer Crystal

    Institute of Scientific and Technical Information of China (English)

    Hongxing LIU; Hong DENG; Yan LI; Yanrong LI

    2004-01-01

    It was focused on the applications and developments of microwave hydrothermal synthesis piezoelectric ceramic powder. The microwave hydrothermal vessel was designed and manufactured. The microwave hydrothermal synthesis system was established and the PZT piezoelectric ceramic powder was synthesized. XRD and TEM have been used to characterize the products in detail. The diameter of the PZT powder particle is from 40 to 60 nm.

  16. Structure and properties of solid-state synthesized poly (3,4-propylenedioxythiophene)/nano-ZnO composite

    Institute of Scientific and Technical Information of China (English)

    Ahmat Ali; Ruxangul Jamal; Weiwei shao; Adalet Rahman; Yakupjan Osman; Tursun Abdiryim

    2013-01-01

    Poly(3,4-propylenedioxythiophene)/nano-Zinic Oxide (PProDOT/ZnO) composites with the content of 3-7 wt% nano-ZnO were synthesized by the solid-state method with FeCl3 as oxidant. The structure and morphology of the composites were characterized by Fourier transform infrared (FTIR) spectroscopy, ultraviolet-visible (UV-vis) absorption spectroscopy, X-ray diffraction (XRD) and transmission electron microscopy (TEM). The electrochemical performances of the composites were investigated by galvanostatic charge-discharge, cyclic voltammetry and electrochemical impedance spectroscopy (EIS). The photocatalytic activities of the composites were investigated by the degradation of methylene blue (MB) dyes in aqueous medium under UV light irradiation. The results from FTIR and UV-vis spectra showed that the PProDOT/ZnO composites were successfully synthesized by solid-state method, and nano-ZnO had great influences on the conjugation length and oxidation degree of the polymers. Furthermore, the PProDOT/5 wt%ZnO had the highest conjugation and oxidation degree among the composites. The results of XRD analysis indicated that there were some FeC14? ions as doping agent in the PProDOT matrix, and the content of ZnO had no effect on diffraction pattern of PProDOT. Morphological studies revealed that the pure PProDOT and composites had similar morphological structure, and all the composites displayed an irregular sponge like morphology. The results of electrochemical tests showed that the PProDOT/5 wt%ZnO had a higher electrochemical activity with a specific capacitance value of 220 Fg ? 1 than others. The results from photocatalytic activities of the composites indicated that the PProDOT/5 wt%ZnO had better photocatalytic activity than other composites.

  17. Relationship between Crystal Shape, Photoluminescence, and Local Structure in SrTiO3 Synthesized by Microwave-Assisted Hydrothermal Method

    Directory of Open Access Journals (Sweden)

    Luís F. da Silva

    2012-01-01

    Full Text Available This paper describes the effect of using different titanium precursors on the synthesis and physical properties of SrTiO3 powders obtained by microwave-assisted hydrothermal method. X-ray diffraction measurements, X-ray absorption near-edge structure (XANES spectroscopy, field emission scanning electron microscopy (FE-SEM, and high-resolution transmission electron microscopy (HRTEM were carried out to investigate the structural and optical properties of the SrTiO3 spherical and cubelike-shaped particles. The appropriate choice of the titanium precursor allowed the control of morphological and photoluminescence (PL properties of SrTiO3 compound. The PL emission was more intense in SrTiO3 samples composed of spherelike particles. This behavior was attributed to the existence of a lower amount of defects due to the uniformity of the spherical particles.

  18. Hydrothermal synthesis of FeWO{sub 4}-graphene composites and their photocatalytic activities under visible light

    Energy Technology Data Exchange (ETDEWEB)

    He, Gang-Ling; Chen, Ming-Jie; Liu, You-Qin; Li, Xin; Liu, Ying-Ju; Xu, Yue-Hua, E-mail: xuyuehua@scau.edu.cn

    2015-10-01

    Graphical abstract: - Highlights: • FeWO{sub 4}-RGO composites were hydrothermally fabricated by facile one-step method. • FeWO{sub 4}-RGO and FeWO{sub 4} had a similar particle size, in the range of 30–50 nm. • High efficiency for photocatalytic degradation of RhB was exhibited by FeWO{sub 4}-RGO. • FeWO{sub 4}-xRGO showed higher photocatalytic activities than pure FeWO{sub 4}. • The electron–hole pairs can be effectively separated due to RGO coupling. - Abstract: Monoclinic ferberite FeWO{sub 4}-reduced graphene oxide (FeWO{sub 4}-RGO) composites were hydrothermally fabricated by facile one-pot method in situ reduction of graphene oxide. As-prepared FeWO{sub 4}-RGO photocatalysts were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectra, and diffuse reflectance spectra (DRS). The FeWO{sub 4}-RGO photocatalysts and pure FeWO{sub 4} photocatalyst had a similar particle size, which was in the range of 30–50 nm. FeWO{sub 4} and FeWO{sub 4}-RGO photocatalysts showed absorption in the visible region, and the band gap energy of FeWO{sub 4} decreased slightly after RGO coupling. FeWO{sub 4}-RGO photocatalysts exhibited high efficiencies in photocatalytic degradation of dye pollutant Rhodamine B (RhB) in solution under visible light irradiation (a 4 W Light Emitting Diode lamp). All FeWO{sub 4}-RGO photocatalysts under visible light showed higher photocatalytic activities than pure FeWO{sub 4} photocatalyst, and FeWO{sub 4}-0.3RGO showed the best photocatalytic activity. The FeWO{sub 4}-RGO composites were formed through the chemical contact between nanometer FeWO{sub 4} particles and RGO, and RGO could act as a good electron acceptor. The enhancement in visible-light photocatalytic performance may be mainly attributed to the effective separation of the photogenerated electron–hole pairs.

  19. An Investigation on the Microstructure of Multi-phase Composite Coatings Synthesized by Plasma Spraying Self-reaction Composite Powders

    Institute of Scientific and Technical Information of China (English)

    DONGYan-chun; YANDian-ran; HeJi-ning; LiXiang-zhi; ZHANGJian-xin; NIUEr-wu

    2004-01-01

    Multi-phase self-reacLion composite (denoted as MPc) coatings containing ceramic and metal multi-phases were fabricated by plasma spraying Fe2O3-Al composite powders. This technology successfully combines self-propagating high-temperature synthesis with plasma spraying. The morphology of the composite powders was examined by scanning electron microscope (SEM). The phase composition and microstructure of the composite coating are studied.

  20. An Investigation on the Microstructure of Multi-phase Composite Coatings Synthesized by Plasma Spraying Self-reaction Composite Powders

    Institute of Scientific and Technical Information of China (English)

    DONG Yan-chun; YAN Dian-ran; HE Ji-ning; LI Xiang-zhi; ZHANG Jian-xin; NIU Er-wu

    2004-01-01

    Multi-phase self-reaction composite (denoted as MPc) coatings containing ceramic and metal multi-phases were fabricated by plasma spraying Fe2O3-Al composite powders. This technology successfully combines self-propagating high-temperature synthesis with plasma spraying. The morphology of the composite powders was examined by scanning electron microscope (SEM). The phase composition and microstructure of the composite coating are studied.

  1. Investigation of laundering and dispersion approaches for silica and calcium phosphosilicate composite nanoparticles synthesized in reverse micelles

    Science.gov (United States)

    Tabakovic, Amra

    Nanotechnology, the science and engineering of materials at the nanoscale, is a booming research area with numerous applications in electronic, cosmetic, automotive and sporting goods industries, as well as in biomedicine. Composite nanoparticles (NPs) are of special interest since the use of two or more materials in NP design imparts multifunctionality on the final NP constructs. This is especially relevant for applications in areas of human healthcare, where the use of dye or drug doped composite NPs is expected to improve the diagnosis and treatment of cancer and other serious illnesses. Since the physicochemical properties of NP suspensions dictate the success of these systems in biomedical applications, especially drug delivery of chemotherapeutics, synthetic routes which offer precise control of NP properties, especially particle diameter and colloidal stability, are utilized to form a variety of composite NPs. Formation of NPs in reverse, or water-in-oil, micelles is one such synthetic approach. However, while the use of reverse micelles to form composite NPs offers precise control over NP size and shape, the post-synthesis laundering and dispersion of synthesized NP suspensions can still be a challenge. Reverse micelle synthetic approaches require the use of surfactants and low dielectric constant solvents, like hexane and cyclohexane, as the oil phase, which can compromise the biocompatibility and colloidal stability of the final composite NP suspensions. Therefore, appropriate dispersants and solvents must be used during laundering and dispersion to remove surfactant and ensure stability of synthesized NPs. In the work presented in this dissertation, two laundering and dispersion approaches, including packed column high performance liquid chromatography (HPLC) and centrifugation (sedimentation and redispersion), are investigated for silver core silica (Ag-SiO2) and calcium phosphosilicate (Caw(HxPO4)y(Si(OH)zOa) b · cH2O, CPS) composite NP suspensions

  2. Electrochemical hydrogen storage performance of AB_5-CoB composites synthesized by a simple mixing method

    Institute of Scientific and Technical Information of China (English)

    SONG Dawei; WANG Yijing; WANG Yaping; JIAO Lifang; YUAN Huatang

    2009-01-01

    AB5 (MINi_(4.0)Al_(0.3)Cu_(0.5)Zn_(0.2)) alloy and CoB alloy were prepared by arc melting. AB_5-CoB composites were synthesized by simple mixing of AB_5 alloy powders and CoB alloy powders, and their electrochemical hydrogen storage properties were studied as negative electrodes in KOH aqueous solution. The maximum discharge capacity of the AB_5-CoB(50%) composite (the content of CoB in the composite is 50 wt.%) reached 365.3 mAh·g~(-1). After 100 charge-discharge cycles, the discharge capacity of the AB_5-CoB(50%) composite was still much higher than that of the AB5 alloy. The high rate discharge capability (HRD) and potentiodynamic polarzafion were also tested.

  3. Template-assisted hydrothermally obtained titania-ceria composites and their application as catalysts in ethyl acetate oxidation and methanol decomposition with a potential for sustainable environment protection

    Science.gov (United States)

    Tsoncheva, Tanya; Mileva, Alexandra; Issa, Gloria; Dimitrov, Momtchil; Kovacheva, Daniela; Henych, Jiří; Scotti, Nicola; Kormunda, Martin; Atanasova, Genoveva; Štengl, Vaclav

    2017-02-01

    High surface area mesoporous ceria-titania binary materials with high Lewis acidity and improved reduction properties were synthesized using template assisted hydrothermal technique. The obtained materials were characterized by low temperature nitrogen physisorption, XRD, SEM, TEM, Raman, UV-vis, XPS, FTIR, FTIR of adsorbed pyridine and thermo-programmed reduction with hydrogen. Their catalytic activity was tested in total oxidation of ethyl acetate and methanol decomposition to CO and hydrogen with a potential application in VOCs elimination and alternative fuels, respectively. The structural changes in the binary materials, which could be tuned by the variation in the Ce/Ti ratio and the temperature of hydrothermal treatment, provoked significant changes in their textural, surface and redox properties, which is in close relation to the catalytic activity and selectivity in various catalytic processes. The intimate contact between the individual oxides results in the formation of different catalytic active sites and their role in the studied catalytic reactions was discussed in details.

  4. Major and trace element composition of surface sediments from the Southwest Indian Ridge: evidence for the incorporation of a hydrothermal component

    Institute of Scientific and Technical Information of China (English)

    LI Zhenggang; CHU Fengyou; JIN Lu; LI Xiaohu; DONG Yanhui; CHEN Ling; ZHU Jihao

    2016-01-01

    Hydrothermal materials in deep-sea sediments provide a robust tracer to the localized hydrothermal activity at mid-ocean ridges. Major, trace and rare earth element (REE) data for surface sediments collected from the ultraslow spreading Southwest Indian Ridge are presented to examine the existence of hydrothermal component. Biogenic carbonate oozes dominate all the sediment samples, with CaO content varying from 85.5% to 89.9% on a volatile-free basis. The leaching residue of bulk sediments by ~5% HCl is compositionally comparable to the Upper Continental Crust (UCC) in SiO2, Al2O3, CaO, MgO, alkali elements (Rb, Cs) and high field strength elements (Nb, Ta, Zr, Hf, Ti). These detritus-hosted elements are inferred to be prominently derived from the Australian continent by means of eolian dust, while the contribution of local volcaniclastics is insignificant. In addition, the residual fraction shows a clear enrichment in Fe, Mn, and Ba compared with the UCC. Combining the positive Eu anomaly of residual fraction which is opposed to the UCC but the characteristic of hydrothermal fluids and associated precipitates occurred at mid-ocean ridges, the incorporation of localized hydrothermal component can be constrained. REE mixing calculations indicate that more than half REE within the residual fraction (~55%–60%) are derived from a hydrothermal component, which is inferred to be resulted from a diffuse fluid mineralization. The low-temperature diffuse flow may be widely distributed along the slow-ultraslow spreading ridges where crustal faults and fissures abound, and probably have a great mineralization potential.

  5. Vacancy-induced room-temperature ferromagnetism in ZnO rods synthesized by Ni-doped solution and hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Yu Zhenhua [Key Laboratory for Magnetism and Magnetic Materials of Ministry of Education, Lanzhou University, Lanzhou 730000 (China); Ge Shihui, E-mail: gesh@lzu.edu.cn [Key Laboratory for Magnetism and Magnetic Materials of Ministry of Education, Lanzhou University, Lanzhou 730000 (China); Zuo Yalu; Wang Guowei; Zhang Feng [Key Laboratory for Magnetism and Magnetic Materials of Ministry of Education, Lanzhou University, Lanzhou 730000 (China)

    2010-08-01

    Pure ZnO and Ni-doped ZnO rods have been prepared by hydrothermal method at a temperature of 120 deg. C. The morphological, structural, magnetic and optical properties of the as-prepared rods were investigated by means of field emission scanning electron microscopy, X-ray diffraction, vibrating sample magnetometer and photoluminescence. All the samples are radial-grown hexagon rods with diameter from 470 to 720 nm and length of 4-6 {mu}m. X-ray diffraction shows that the rods have single crystalline wurtzite structure without other impurity phases. The pure ZnO rods and Ni-doped ZnO rods have ferromagnetism at room temperature, and the special saturation magnetization deduces with the increasing diameter of rods. These results reveal that the saturation magnetization of the ZnO rods depends on the surface-to-volume ratio of rods rather than the Ni doping concentrations. The photoluminescence spectra studies show the same diameter dependences of oxygen vacancies as that of magnetization, which demonstrates that oxygen vacancies at surface of rods play an important role in introducing ferromagnetism. The annealing in rich oxygen and reducing atmospheres confirms this argument further.

  6. Structure and photoluminescence properties of Ce0.5Zr0.5O2:Eu3+ nanoparticles synthesized by hydrothermal method

    Science.gov (United States)

    Ozawa, Masakuni; Yoshimura, Yusuke; Kobayashi, Katsutoshi

    2017-01-01

    Eu3+-doped Ce0.5Zr0.5O2 nanocrystals were prepared by a hydrothermal method. The structural and optical properties of the samples were characterized by X-ray diffraction, Raman scattering and photoluminescence spectra. No luminescence was observed for Ce0.5Zr0.5O2, while Ce0.5Zr0.5O2:Eu3+ nanoparticles as-prepared and calcined at 400 °C showed emission due to Eu3+. The emission spectrum of the Eu3+ site shows that the total intensity decreases with increasing concentration of Eu3+ from 1 to 10% in Ce0.5Zr0.5O2. The broad band in the excitation spectrum of calcined Ce0.5Zr0.5O2:Eu3+ originates from the charge transfer (CT) transition. The local distortion and the asymmetry factor around the Eu3+ centers were discussed with the Raman and photoluminescence spectra. The present study provides both knowledge expected to lead to novel nanocrystal phosphor materials and a useful measure for analyzing the catalytic properties of nanocrystalline Ce0.5Zr0.5O2.

  7. Effect of HNO3 Concentration on the Morphologies and Properties of Bi2WO6 Photocatalyst Synthesized by a Hydrothermal Method

    Directory of Open Access Journals (Sweden)

    Wenjie Wang

    2016-07-01

    Full Text Available Bi2WO6 samples were prepared by a hydrothermal method using Bi(NO33·5H2O and Na2WO4·2H2O as raw materials. X-ray diffraction (XRD, field-emission scanning electron microscopy (FESEM, Raman and Brunauer–Emmett–Teller (BET were employed for sample characterization. The photocatalytic activity of the samples was evaluated by the degradation of Rhodamine B under visible-light irradiation. The photocatalytic activity of Bi2WO6, as well as the effect of varying HNO3 concentrations on the morphologies of Bi2WO6, was investigated. The HNO3 concentration significantly affected the structure and morphology of the Bi2WO6. The photocatalytic performance varied with the structure, morphology, and surface area of the Bi2WO6 samples. The results indicated that the H10 sample exhibits uniform morphology and excellent photocatalytic performance; using this sample, the degradation of Rhodamine B reached 96% in 90 min under visible-light irradiation.

  8. Structural studies of BaTiO3:Er3+and BaTiO3:Yb3+powders synthesized by hydrothermal method

    Institute of Scientific and Technical Information of China (English)

    Garrido-Hernndez A; Garca-Murillo A; Carrillo-Romo Fde J; Cruz-Santiago LA; Chadeyron G; Morales-Ramrez Ade J; Velumani S

    2014-01-01

    Erbium and ytterbium doped barium titanate nanopowders were prepared using the hydrothermal method. A barium titan-ate structure doped with rare earth ions manifested new characteristics and improved the field of application of optical devices such as trichromatic tubes, LCD displays, lamps, and infrared lasers. In this work, BaTiO3:Er3+and BaTiO3:Yb3+were prepared using barium chloride [BaCl2], titanium butoxide [C16H36O4Ti], erbium chloride [ErCl3] and ytterbium chloride [YbCl3] as precursors. Anhydrous methanol was employed as a solvent. Metallic potassium was used to promote solubility in the system and increase the pH to 13. This method yielded the formation of a predominantly cubic structure in both Er3+and Yb3+doped BaTiO3 powders. Characteristic bond-ings of BaTiO3 were observed with FT-IR spectroscopy. The predominantly cubic structure was confirmed by X-ray diffraction and micro-Raman analyses. The particle size (∼30 nm) was estimated using the Scherrer equation and X-ray diffraction data. The results were presented and discussed.

  9. Hydrothermal synthesis of magnetic Fe3O4/graphene composites with good electromagnetic microwave absorbing performances

    Science.gov (United States)

    Zhu, Lingyu; Zeng, Xiaojun; Li, Xiaopan; Yang, B.; Yu, Ronghai

    2017-03-01

    The Fe3O4 sub-microspheres have been embedded uniformly into the reduced graphene oxide (rGO) to form a new-type Fe3O4/rGO composites through a one-pot solvothermal method. The dielectric properties for these magnetic Fe3O4/rGO composites can be greatly tuned by their different rGO additions. A good impedance matching from the balanced dielectric and magnetic loss is achieved in the Fe3O4/rGO composites with 4 wt% rGO addition, which dominates their excellent microwave absorbing performances including the minimum reflection loss (RL) value of -45 dB at a frequency of 8.96 GHz with a sample thickness of 3.5 mm and an effective absorption bandwidth of 3.2 GHz (below -10 dB) superior to those of the most magnetic materials and carbon-based composites. The controlled Fe3O4/rGO composite structure also exhibits high chemical stability and low density, which shows great potential application in high-performance electromagnetic microwave-absorbing materials.

  10. Hybrid polymer composites reinforced by layered silicate and laser synthesized nanocarbons

    Science.gov (United States)

    Dinca, I.; Stefan, A.; Serghie, C.; Moga, A.; Dumitrache, L.; Vuluga, Z.; Donescu, D.; Dragomirescu, A.; Prodan, G.; Ciupina, V.; Gavrila-Florescu, L.; Popovici, E.; Sandu, I.

    2007-12-01

    The work presents some preliminary results obtained in the attempt to perform hybrid polymer-based nanocomposites with laser synthesized carbon nanostructures and layered silicate. The preliminary results suggest that there is a close relation between the improved characteristics of the obtained nanocomposite and filler's properties. Laser synthesized nanocarbons, from almost amorphous up to fullerenic-like structure were used. As layered silicate, a modified Cloisite-type montmorillonite is mentioned. Preliminary results suggest that some of these addition agents lead to samples of nanocomposites with significant improvement of their aimed properties.

  11. Hydrothermal ageing of glass/epoxy composites for wind turbine blades

    NARCIS (Netherlands)

    Rocha, I.B.C.M.; Raijmaekers, S.; Nijssen, R.P.L.; Van der Meer, F.P.

    2015-01-01

    In this work, a glass/epoxy material system commonly applied in wind turbine design was used to evaluate damage processes brought by water ingression during service life. Composite short-beams and neat epoxy beams and dog-bones were conditioned by water immersion at 50º until saturation and tested b

  12. The Influences of Disperse and Pre—composite on Synthesized AT

    Institute of Scientific and Technical Information of China (English)

    SUNJiejing; LIUYongjie

    1996-01-01

    The microstructure of synthesized AT(A-luminum titanate) has been improved efficient-ly,And the microcrack of AT formed during cooling and abnormal grain growth have been limitd.Therefore,the sinterability and mechanical properties of AT material have been enhanced.

  13. CERAMIC MATRIX COMPOSITE SYNTHESIZED BY THE PURE Al+NaOH SELF-OXIDATION

    Institute of Scientific and Technical Information of China (English)

    S.X.He; S.Yuan; J.Wang; B.D.Sun

    2001-01-01

    An Al2 O3/Al ceramic matrix composite was fabricated by self-oxidation of pureAl+ NaOH,and its microstructure,mechanical properties and 9rowth mechanism wereanalyzed.Experimental results show that the composite possesses better mechanicalproperties,higher density and faster growth velocity than that made by Al-Mg-Si al-loy.The composite grows primarily along the crucible wall and has periodic wavy likestructure consisted with cell colonies.

  14. Ultrafast hydrothermal synthesis of high quality magnetic core phenol-formaldehyde shell composite microspheres using the microwave method.

    Science.gov (United States)

    You, Li-Jun; Xu, Shuai; Ma, Wan-Fu; Li, Dian; Zhang, Yu-Ting; Guo, Jia; Hu, Jack J; Wang, Chang-Chun

    2012-07-17

    An ultrafast, facile, and efficient microwave hydrothermal approach was designed to fabricate magnetic Fe(3)O(4)/phenol-formaldehyde (PF) core-shell microspheres for the first time. The structure of the Fe(3)O(4)/PF core-shell microspheres could be well controlled by the in situ polycondensation of phenol and formaldehyde with magnetic Fe(3)O(4) clusters as the seeds in an aqueous solution without any surfactants. The effect of synthetic parameters, such as the feeding amounts of phenol, the dosages of formaldehyde, the reaction temperatures, and the microwave heating time, on the morphologies and sizes of the Fe(3)O(4)/PF microspheres were investigated in details. The phenol-formaldehyde shell is found to be evenly coated on Fe(3)O(4) clusters within 10 min of the irradiation. The as-prepared microspheres were highly uniform in morphology, and the method was found to allow the shell thickness to be finely controlled in the range of 10-200 nm. The properties of the composite microspheres were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), thermogravimetic analysis (TGA), Fourier transform infrared (FT-IR) spectra, X-ray diffraction (XRD), and vibrating sample magnetometer (VSM). The as-prepared Fe(3)O(4)/PF microspheres were monodisperse and highly dispersible in water, ethanol, N,N-dimethyformamide, and acetone, a beneficial quality for the further functionalization and applications of the Fe(3)O(4)/PF microspheres.

  15. Structural, electrical, optical and analytical applications of newly synthesized polyaniline based nickel molybdate composite

    Energy Technology Data Exchange (ETDEWEB)

    Khan, Meraj Alam; Ishrat, Urfi; Dar, Ayaz Mahmood; Ahmad, Anees, E-mail: aneesahmad@yahoo.com

    2015-07-05

    Highlights: • Synthesis of organic–inorganic conducting nano-composite cation-exchanger. • Average particle size was found to be 76 nm. • The nano-composite was found to be selective for Pb(II), Hg(II) and Th(IV) ions. • The nano composite indicated a band gap of about 3.44 eV showing a weak blue shift compared to 3.37 eV. • The binary separations of metal ions are fairly sharp and reproducible with 90–95% recovery. - Abstract: The synthesis of polyaniline based nickel molybdate nano composite cation exchanger was described by sol–gel method and was explored to study the electrical, optical and analytical applications. The nano composite material was characterized by Fourier Transform Infrared (spectrometer), X-ray diffraction, particle size analyzer, scanning electron microscopy and tunneling electron microscopy. The XRD of nano composite material confirmed the semi-crystalline nature while as particle size analysis as well as TEM depicted average particle size of 76 nm. The partition coefficient studies of different metal ions in the composite were performed in demineralised water and sodium dodecyl sulfate surfactant, and it was found to be selective for Pb(II), Hg(II) and Th(IV) ions. To implement the use of polyaniline Ni(II) molybdate nano composite as adsorbent, some important binary separations of metal ions were performed. SEM analysis showed that the nano composite has random non-preferential orientation with no visible cracks and appeared to be composed of dense and loose aggregation of small particles. The UV–vis spectrum of the nano composite indicated a band gap of about 3.44 eV showing a weak blue shift compared to 3.37 eV for the bulk. Due to their optical and electrical properties, nano composite is promising candidate for use as selectivity of different cations.

  16. Microstructural and hardness behavior of graphene-nanoplatelets/aluminum composites synthesized by mechanical alloying

    Energy Technology Data Exchange (ETDEWEB)

    Pérez-Bustamante, R. [Centro de Investigación en Materiales Avanzados (CIMAV), Laboratorio Nacional de Nanotecnología, Miguel de Cervantes No. 120, C.P. 31109 Chihuahua, Chih. (Mexico); Bolaños-Morales, D.; Bonilla-Martínez, J. [Universidad Autónoma de Chihuahua (UACH), Facultad de Ingeniería, Circuito No. 1 Nuevo Campus Universitario, C.P. 31125 Chihuahua, Chih. (Mexico); Estrada-Guel, I. [Centro de Investigación en Materiales Avanzados (CIMAV), Laboratorio Nacional de Nanotecnología, Miguel de Cervantes No. 120, C.P. 31109 Chihuahua, Chih. (Mexico); Martínez-Sánchez, R., E-mail: roberto.martinez@cimav.edu.mx [Centro de Investigación en Materiales Avanzados (CIMAV), Laboratorio Nacional de Nanotecnología, Miguel de Cervantes No. 120, C.P. 31109 Chihuahua, Chih. (Mexico)

    2014-12-05

    Highlights: • Pure aluminum was reinforced with graphene-platelets by using mechanical milling. • The composites were studied after sintering condition. • Milling time and graphene-platelet enhance the mechanical behavior of the composites. - Abstract: Graphene can be considered as an ideal reinforcement for the production of composites due to its outstanding mechanical properties. These characteristics offer an increased opportunity for their study in the production of metal matrix composites (MMCs). In this research, the studied composites were produced by mechanical alloying (MA). The employed milling times were of 1, 3 and 5 h. GNPs were added in 0.25, 0.50 and 1.0 wt% into an aluminum powder matrix. Milled powders were cold consolidated and subsequently sintered. Composites were microstructurally characterized with Raman spectroscopy and electron microscopy and X-ray diffraction. The hardness behavior in composites was evaluated with a Vickers micro-hardness test. A homogeneous dispersion of graphene during MA and the proper selection of sintering conditions were considered to produce optimized composites. The obtained results with electron microscopy indicate a homogeneous dispersion of GNPs into the aluminum matrix. Analyses showed GNPs edges where the structure of the graphene layers conserved after MA is observed.

  17. Electrochemical performance of Si@TiN composite anode synthesized in a liquid ammonia for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Tu, Jiguo; Wang, Wei [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Jiao, Shuqiang, E-mail: sjiao@ustb.edu.cn [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Hou, Jungang; Huang, Kai [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Zhu, Hongmin, E-mail: hzhu@metall.ustb.edu.cn [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China)

    2012-10-15

    High-efficiency Si@TiN composite anode was synthesized by a homogeneous reduction reaction in the liquid ammonia, then calcinated at 950 Degree-Sign C for 2 h in vacuum. The crystal structure and morphology of the obtained in-situ coated composites were characterized by XRD, FESEM. The results showed that the micron-sized Si particles were almost coated by the TiN nanoparticles with the average size of 50 nm, while the morphology of Si@TiN composite was almost unchanged over 50 discharge-charge cycles. The electrochemical performances of Si@TiN composite anode were studied by galvanostatic discharge-charge tests, cyclic voltammetry (CV) and electrochemical impedance spectrum (EIS). The CV curves showed that the two redox peaks remained stable and were attributed to the alloying/dealloying process of Li with active Si particles. It could be seen from the EIS curves that the charge transfer resistance (R{sub ct}) for fresh was larger than that for the 50th cycle, which was mainly because the electrons and Li ions conducted on the electrode surface more difficultly for fresh. The cycle stability of the as-prepared Si@TiN composite anode was investigated, with the result showing that the cycling performance was stable and optimal at a rate of 0.2 C. The initial charge capacity was as high as 3226.99 mAh g{sup -1}, which was kept as 467.02 mAh g{sup -1} over 50 cycles. -- Highlights: Black-Right-Pointing-Pointer Si@TiN composite anode was synthesized in-situ in a liquid ammonia. Black-Right-Pointing-Pointer The size of TiN nanoparticles was about 50 nm. Black-Right-Pointing-Pointer The initial charge capacity was as high as 3226.99 mAh g{sup -1}.

  18. Hydrothermal liquefaction of biomass

    DEFF Research Database (Denmark)

    Toor, Saqib; Rosendahl, Lasse; Rudolf, Andreas

    2011-01-01

    This article reviews the hydrothermal liquefaction of biomass with the aim of describing the current status of the technology. Hydrothermal liquefaction is a medium-temperature, high-pressure thermochemical process, which produces a liquid product, often called bio-oil or bi-crude. During...... the hydrothermal liquefaction process, the macromolecules of the biomass are first hydrolyzed and/or degraded into smaller molecules. Many of the produced molecules are unstable and reactive and can recombine into larger ones. During this process, a substantial part of the oxygen in the biomass is removed...... by dehydration or decarboxylation. The chemical properties of bio-oil are highly dependent of the biomass substrate composition. Biomass constitutes of various components such as protein; carbohydrates, lignin and fat, and each of them produce distinct spectra of compounds during hydrothermal liquefaction...

  19. Did the massive magnetite "lava flows" of El Laco (Chile) form by magmatic or hydrothermal processes? New constraints from magnetite composition by LA-ICP-MS

    Science.gov (United States)

    Dare, Sarah A. S.; Barnes, Sarah-Jane; Beaudoin, Georges

    2015-06-01

    The El Laco magnetite deposits consist of more than 98 % magnetite but show field textures remarkably similar to mafic lava flows. Therefore, it has long been suggested that they represent a rare example of an effusive Fe oxide liquid. Field and petrographic evidence, however, suggest that the magnetite deposits represent replacement of andesite flows and that the textures are pseudomorphs. We determined the trace element content of magnetite by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) from various settings at El Laco and compared them with magnetite from both igneous and hydrothermal environments. This new technique allows us to place constraints on the conditions under which magnetite in these supposed magnetite "lava flows" formed. The trace element content of magnetite from the massive magnetite samples is different to any known magmatic magnetite, including primary magnetite phenocrysts from the unaltered andesite host rocks at El Laco. Instead, the El Laco magnetite is most similar in composition to hydrothermal magnetite from high-temperature environments (>500 °C), such as iron oxide-copper-gold (IOCG) and porphyry-Cu deposits. The magnetite trace elements from massive magnetite are characterised by (1) depletion in elements considered relatively immobile in hydrothermal fluids (e.g. Ti, Al, Cr, Zr, Hf and Sc); (2) enrichment in elements that are highly incompatible with magmatic magnetite (rare earth elements (REE), Si, Ca, Na and P) and normally present in very low abundance in magmatic magnetite; (3) high Ni/Cr ratios which are typical of magnetite from hydrothermal environments; and (4) oscillatory zoning of Si, Ca, Mg, REE and most high field strength elements, and zoning truncations indicating dissolution, similar to that formed in hydrothermal Fe skarn deposits. In addition, secondary magnetite in altered, brecciated host rock, forming disseminations and veins, has the same composition as magnetite from the massive

  20. Structural characterization and property of in-situ synthesized AZ91-Mg2Si composite

    Institute of Scientific and Technical Information of China (English)

    DONG Long-xiang; WU Yao-ming; DOU Chuan-guo; XU Guo-gen; WANG Li-min

    2006-01-01

    A new-type Mg2Si composite was prepared with Mg-9Al-1Zn (AZ91) alloy and vermiculite as raw materials by melt infiltration method. The results show that the microstructure of composite consists of a large amount of Mg2Si precipitates and a little amount of MgO embedded in α-Mg matrix. The Vickers hardness of the composite is obviously higher than that of matrix of AZ91 alloy. Moreover, the composite exhibits excellent compressive property. The ultimate compressive strength of the material is 290 MPa, the yield strength is 175 MPa, and the elongation is about 5%, which are higher than those of AZ91alloy.

  1. Mechanochemically synthesized kalsilite based bioactive glass-ceramic composite for dental vaneering

    Science.gov (United States)

    Kumar, Pattem Hemanth; Singh, Vinay Kumar; Kumar, Pradeep

    2017-08-01

    Kalsilite glass-ceramic composites have been prepared by a mechanochemical synthesis process for dental veneering application. The aim of the present study is to prepare bioactive kalsilite composite material for application in tissue attachment and sealing of the marginal gap between fixed prosthesis and tooth. Mechanochemical synthesis is used for the preparation of microfine kalsilite glass-ceramic. Low temperature frit and bioglass have been prepared using the traditional quench method. Thermal, microstructural and bioactive properties of the composite material have been examined. The feasibility of the kalsilite to be coated on the base commercial opaque as well as the bioactive behavior of the coated specimen has been confirmed. This study indicates that the prepared kalsilite-based composites show similar structural, morphological and bioactive behavior to that of commercial VITA VMK95 Dentin 1M2.

  2. Mechanochemically synthesized kalsilite based bioactive glass-ceramic composite for dental vaneering

    Science.gov (United States)

    Kumar, Pattem Hemanth; Singh, Vinay Kumar; Kumar, Pradeep

    2015-08-01

    Kalsilite glass-ceramic composites have been prepared by a mechanochemical synthesis process for dental veneering application. The aim of the present study is to prepare bioactive kalsilite composite material for application in tissue attachment and sealing of the marginal gap between fixed prosthesis and tooth. Mechanochemical synthesis is used for the preparation of microfine kalsilite glass-ceramic. Low temperature frit and bioglass have been prepared using the traditional quench method. Thermal, microstructural and bioactive properties of the composite material have been examined. The feasibility of the kalsilite to be coated on the base commercial opaque as well as the bioactive behavior of the coated specimen has been confirmed. This study indicates that the prepared kalsilite-based composites show similar structural, morphological and bioactive behavior to that of commercial VITA VMK95 Dentin 1M2.

  3. FORMATION MECHANISM OF TITANIUM CARBIDE CRYSTAL IN LASER SYNTHESIZED METAL-CERAMIC COMPOSITE COATING

    OpenAIRE

    BAOSHUAI DU; ZHONGWEN. ZHANG; XINHONG WANG; ZENGDA ZOU

    2011-01-01

    In situ titanium carbide reinforced iron-based composite coating was deposited on mild carbon steel using laser surface engineering (LSE) with ferrotitanium and graphite as precursor. The microstructure and phase constituents of the deposited coating were characterized. Formation mechanism of titanium carbide crystal in the composite coating was elucidated by correlating the morphology of titanium carbide and the thermal cycle experienced by the precursor during the laser treatment. It was de...

  4. A Facile Route to Synthesize Nanographene Reinforced PBO Composites Fiber via in Situ Polymerization

    Directory of Open Access Journals (Sweden)

    Mingqiang Wang

    2016-07-01

    Full Text Available The polymer matrix with introduced carbon-based nanofiber displays fascinating properties. They have inspired extensive research on the synthesis of polymer composites, which have been applied in catalysis, electronics, and energy storage. In this report, we reported a facile and efficient method to prepare poly(p-phenylene benzobisoxazole (PBO/nanographene (PNG composites fibers via in-situ polymerization, accompanied by the reduction from (nanographene oxide NGO to (nanographene NG. By tuning the ratio of feeding PBO monomer to NGO, various composites fibers with 0.1–1 wt % contents of NG were obtained. The efficient PBO chains grafting made NG uniformly disperse in the PBO matrix, and it also increased the uniformity of the packing orientation of PBO chains. Consequently, the tensile strength, tensile modulus, and thermal stability of the obtained PNG composites fibers had been improved significantly. In addition, the composites fibers with 0.5 wt % NG exhibited a 25% increment in tensile strength, and a 41% enhancement in tensile modulus compared with neat PBO fibers. It reveals an excellent reinforcement to PBO composites fibers with NG.

  5. Study on hydrothermal synthesized gepolymer materials based on metakaolin-fly ash%水热合成法制备偏高岭土-粉煤灰基地聚合物材料的研究

    Institute of Scientific and Technical Information of China (English)

    唐婕; 陈益兰; 周君生

    2011-01-01

    Zeolite-enhanced geopolymer were hydrothermal synthesized with sodium hydroxide as alkali activator,fly ash and metakaolin as raw materials. The influences of fly ash content,sodium hydroxide solution concentration,steam-curing temperature and steam-curing time on the mechanical properties of materials were discussed. The results show that different factors have different influence on the strength,with sodium hydroxide solution concentration most prominent. With the conditions of fly ash content of 50%,sodium hydroxide solution concentration of 10 mol/L,steam-curing temperature of 100℃ and steam-curing time of 24 hours,the strength of geopolymer can reach 47.5 MPa in three days. Amorphous silicon aluminum acid salt and zeolite were mainly generated in the product by XRD and SEM analysis,and different kinds of zeolites were synthesized at different hydrothermal synthesis process.%以氢氧化钠为激发剂,偏高岭土和粉煤灰为主要原料,采用水热合成法制备沸石增强型地聚合物材料,探讨粉煤灰掺量、氢氧化钠溶液浓度、蒸养时间、蒸养温度等因素对材料力学性能的影响.研究表明:不同因素对地聚合物强度的影响不同,其中以氢氧化钠溶液浓度影响最为突出;当粉煤灰掺量为50%,氢氧化钠溶液浓度为10 mol/L,在100℃下蒸养24 h,试样3d抗压强度达47.5 MPa;通过XRD和SEM分析可知,地聚合物样品主要为无定形的硅铝酸盐及沸石相,随着水热合成工艺条件的改变,生成的沸石类型不同.

  6. Ethanol electrooxidation in alkaline medium on electrochemically synthesized Co(OH)2/Au composite

    Science.gov (United States)

    Babu, Sreejith P.; Elumalai, Perumal

    2017-01-01

    Gold (Au), cobalt hydroxide (Co(OH)2) and different Co(OH)2/Au compositions were electro-deposited onto stainless steel by a potentiodynamic method from the respective metal-ion solutions. The deposits were characterized by x-ray diffraction (XRD), scanning electron microscope (SEM) and Fourier transformed infra-red spectroscopy (FT-IR). The XRD and IR data confirmed that the deposits were Au, α-Co(OH)2 or Co(OH)2/Au composites. The SEM observations confirmed that the morphology of the Au was spherical, while the α-Co(OH)2 was flakey with pores. The morphology of the Co(OH)2/Au composites consisted of highly agglomerated Au grains distributed on the Co(OH)2 matrix. The electrocatalytic activity of each of the Au, Co(OH)2 and Co(OH)2/Au-composite electrodes towards ethanol electrooxidation in an alkaline medium was investigated by cyclic voltammetry and chronoamperometry. It turned out that the Co(OH)2/Au-composite electrodes exhibited superior catalytic activity for ethanol electrooxidation compared with the pristine Au or Co(OH)2 electrodes. A peak current density as high as 25 mA cm‑2 was exhibited by the Co(OH)2/ Au composite while the Au and Co(OH)2 showed only 0.9 and 13 mA cm‑2, respectively. The enhanced conductivity of the Co(OH)2/Au matrix due to the presence of Au, as well as the combined catalytic activity, seemed to be responsible for the superior performance of the Co(OH)2/Au-composite electrodes.

  7. Characterization of boron carbide particulate reinforced in situ copper surface composites synthesized using friction stir processing

    Energy Technology Data Exchange (ETDEWEB)

    Sathiskumar, R., E-mail: sathiscit2011@gmail.com [Department of Mechanical Engineering, Coimbatore Institute of Technology, Coimbatore, 641 014 Tamil Nadu (India); Murugan, N., E-mail: murugan@cit.edu.in [Department of Mechanical Engineering, Coimbatore Institute of Technology, Coimbatore, 641 014 Tamil Nadu (India); Dinaharan, I., E-mail: dinaweld2009@gmail.com [Department of Mechanical Engineering, V V College of Engineering, Tisaiyanvilai, 627 657 Tamil Nadu (India); Vijay, S.J., E-mail: vijayjoseph@karunya.edu [Centre for Research in Metallurgy (CRM), School of Mechanical Sciences, Karunya University, Coimbatore, 641 114 Tamil Nadu (India)

    2013-10-15

    Friction stir processing has evolved as a novel solid state technique to fabricate surface composites. The objective of this work is to apply the friction stir processing technique to fabricate boron carbide particulate reinforced copper surface composites and investigate the effect of B{sub 4}C particles and its volume fraction on microstructure and sliding wear behavior of the same. A groove was prepared on 6 mm thick copper plates and packed with B{sub 4}C particles. The dimensions of the groove was varied to result in five different volume fractions of B{sub 4}C particles (0, 6, 12, 18 and 24 vol.%). A single pass friction stir processing was done using a tool rotational speed of 1000 rpm, travel speed of 40 mm/min and an axial force of 10 kN. Metallurgical characterization of the Cu/B{sub 4}C surface composites was carried out using optical microscope and scanning electron microscope. The sliding wear behavior was evaluated using a pin-on-disk apparatus. Results indicated that the B{sub 4}C particles significantly influenced the area, dispersion, grain size, microhardness and sliding wear behavior of the Cu/B{sub 4}C surface composites. When the volume fraction of B{sub 4}C was increased, the wear mode changed from microcutting to abrasive wear and wear debris was found to be finer. Highlights: • Fabrication of Cu/B{sub 4}C surface composite by friction stir processing • Analyzing the effect of B{sub 4}C particles on the properties of Cu/B4C surface composite • Increased volume fraction of B{sub 4}C particles reduced the area of surface composite. • Increased volume fraction of B{sub 4}C particles enhanced the microhardness and wear rate. • B{sub 4}C particles altered the wear mode from microcutting to abrasive.

  8. Carbon Nanofibers and Their Composites: A Review of Synthesizing, Properties and Applications

    Directory of Open Access Journals (Sweden)

    Lichao Feng

    2014-05-01

    Full Text Available Carbon nanofiber (CNF, as one of the most important members of carbon fibers, has been investigated in both fundamental scientific research and practical applications. CNF composites are able to be applied as promising materials in many fields, such as electrical devices, electrode materials for batteries and supercapacitors and as sensors. In these applications, the electrical conductivity is always the first priority need to be considered. In fact, the electrical property of CNF composites largely counts on the dispersion and percolation status of CNFs in matrix materials. In this review, the electrical transport phenomenon of CNF composites is systematically summarized based on percolation theory. The effects of the aspect ratio, percolation backbone structure and fractal characteristics of CNFs and the non-universality of the percolation critical exponents on the electrical properties are systematically reviewed. Apart from the electrical property, the thermal conductivity and mechanical properties of CNF composites are briefly reviewed, as well. In addition, the preparation methods of CNFs, including catalytic chemical vapor deposition growth and electrospinning, and the preparation methods of CNF composites, including the melt mixing and solution process, are briefly introduced. Finally, their applications as sensors and electrode materials are described in this review article.

  9. A strategy to synthesize graphene-incorporated lignin polymer composite materials with uniform graphene dispersion and covalently bonded interface engineering

    Science.gov (United States)

    Wang, Mei; Duong, Le Dai; Ma, Yifei; Sun, Yan; Hong, Sung Yong; Kim, Ye Chan; Suhr, Jonghwan; Nam, Jae-Do

    2017-08-01

    Graphene-incorporated polymer composites have been demonstrated to have excellent mechanical and electrical properties. In the field of graphene-incorporated composite material synthesis, there are two main obstacles: Non-uniform dispersion of graphene filler in the matrix and weak interface bonding between the graphene filler and polymer matrix. To overcome these problems, we develop an in-situ polymerization strategy to synthesize uniformly dispersed and covalently bonded graphene/lignin composites. Graphene oxide (GO) was chemically modified by 4,4'-methylene diphenyl diisocyanate (MDI) to introduce isocyanate groups and form the urethane bonds with lignin macromonomers. Subsequential polycondensation reactions of lignin groups with caprolactone and sebacoyl chloride bring about a covalent network of modified GO and lignin-based polymers. The flexible and robust lignin polycaprolactone polycondensate/modified GO (Lig-GOm) composite membranes are achieved after vacuum filtration, which have tunable hydrophilicity and electrical resistance according to the contents of GOm. This research transforms lignin from an abundant biomass into film-state composite materials, paving a new way for the utilization of biomass wastes.

  10. Composition tunable cobalt-nickel and cobalt-iron alloy nanoparticles below 10 nm synthesized using acetonated cobalt carbonyl

    Energy Technology Data Exchange (ETDEWEB)

    Schooneveld, Matti M. van, E-mail: M.M.vanSchooneveld@gmail.com; Campos-Cuerva, Carlos; Pet, Jeroen; Meeldijk, Johannes D. [Utrecht University, Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science (Netherlands); Rijssel, Jos van [Utrecht University, Van' t Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science (Netherlands); Meijerink, Andries [Utrecht University, Condensed Matter and Interfaces, Debye Institute for Nanomaterials Science (Netherlands); Erne, Ben H. [Utrecht University, Van' t Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science (Netherlands); Groot, Frank M. F. de, E-mail: F.M.F.deGroot@uu.nl [Utrecht University, Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science (Netherlands)

    2012-08-15

    A general organometallic route has been developed to synthesize Co{sub x}Ni{sub 1-x} and Co{sub x}Fe{sub 1-x} alloy nanoparticles with a fully tunable composition and a size of 4-10 nm with high yield. In contrast to previously reported synthesis methods using dicobalt octacarbonyl (Co{sub 2}(CO){sub 8}), here the cobalt-cobalt bond in the carbonyl complex is first broken with anhydrous acetone. The acetonated compound, in the presence of iron carbonyl or nickel acetylacetonate, is necessary to obtain small composition tunable alloys. This new route and insights will provide guidelines for the wet-chemical synthesis of yet unmade bimetallic alloy nanoparticles.

  11. Tungsten Micropowder/Copper Nanoparticle Core/Shell-Structured Composite Powder Synthesized by Inductively Coupled Thermal Plasma Process

    Science.gov (United States)

    Kim, Kyou-Hyun; Choi, Hanshin; Han, Chulwoong

    2017-01-01

    We here synthesized a Cu nanoparticle-coated W micropowder using in-situ reactive radio frequency thermal plasma with a blended feedstock of tungsten (W) and copper oxide micropowder. The spherical W micropowder improves the packing density and uniformity of the compacted body. On the other hand, the Cu nanoparticles coated on the W micropowder allow the spherical W powders to be compacted by rigid-die compaction only at 400 MPa. Moreover, homogeneous sintering in both solid state and liquid state occurs even at low Cu contents of 5 wt pct due to the uniformly coated Cu nanoparticles. The effect of W/Cu core/shell structure on the physical properties of sintered W-5 wt pct Cu composite is investigated based on the density, resistivity, and hardness. The results show that homogeneously sintered W-5 wt pct Cu composite well agree with the theoretical values calculated from the rule of mixture.

  12. Interface-defect-mediated photocatalysis of mesocrystalline ZnO assembly synthesized in-situ via a template-free hydrothermal approach

    Science.gov (United States)

    Wang, Hui; Wang, Cuicui; Chen, Qifeng; Ren, Baosheng; Guan, Ruifang; Cao, Xiaofeng; Yang, Xiaopeng; Duan, Ran

    2017-08-01

    Both architecture construction and defects engineering of photocatalysts are highly vital in the photocatalytic activity. We report herein that the interface-defect-mediated photocatalytic activity of pompon-like ZnO (P-ZnO) mesocrystal photocatalyst synthesized via an aqueous approach, in the presence of sodium citrate without any other organic templates. The microstructure and defects of the diverse ZnO photocatalysts were examined with various techniques. The results indicated that the P-ZnO assemblies were composed of mesocrystal nanosheets exposed high energy (002) facet with high crystallinity. More importantly, the defects located at the interfaces among the nanocrystals in ZnO mesocrystals played an important role in the photocatalytic activity than that of interstitial zinc vacancies in bulk, which was confirmed by photocatalytic degradation of organic pollutants, such as methylene blue (MB) and 2,4,6-trichlorophenol (2,4,6-TCP). The results showed that the P-ZnO exhibited higher photocatalytic activity than that of the nanosized ZnO (N-ZnO), which could be attributed to not only the unique mesocrystal structure and high energy (002) facet exposed, but also the defects located at interfaces among nanocrystals in ZnO mesocrystals. In addition, the formation mechanism of the P-ZnO was investigated via a time-dependent method. It was found that the formation of P-ZnO hierarchical architecture assembled with ZnO mesocrystals involved a nonclassical crystallization growth and Ostwald Ripening process. This study provides a perspective on the improvement in photocatalytic activity via adjusting the bulk and interface defects and construction of hierarchical architectures of semiconductors.

  13. Friction and wear characteristics of Al-Cu/C composites synthesized using partial liquid phase casting process

    Energy Technology Data Exchange (ETDEWEB)

    Ng, W.B.; Gupta, M.; Lim, S.C. [Department of Mechanical and Production Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore (Singapore)

    1997-10-01

    During the sliding of aluminium alloys dispersed with graphite particulates, a layer of graphite is usually present at the sliding interface. This tribo-layer significantly reduces the amount of direct metal-to-metal contact, giving rise to low friction and a low rate of wear, making these composites useful candidate materials for anti-friction applications. Such self-lubricating composites are commonly fabricated via the squeeze casting, slurry casting or powder metallurgy route. These processes are expensive while the less-expensive conventional casting route is limited by the agglomeration of graphite particles in the composites, giving rise to poor mechanical properties. In this work, graphite particulate-reinforced Al-4.5 wt.% Cu composites with two effective graphite contents (Al-4.5 Cu/4.2 wt.% C and Al-4.5 Cu/6.8 wt.% C) were synthesized through an innovative partial liquid phase casting (rheocasting) technique, which is a modification of the conventional casting process. Unlubricated (without the use of conventional liquid lubrication) friction and wear performance of these composites as well as the un-reinforced aluminium alloy was determined using a pin-on-disk tester. The results revealed that the graphite-reinforced composites have a higher wear rate than the un-reinforced matrix alloy while their frictional characteristics are very similar within the range of testing conditions. Combining these with the information gathered from worn-surface examinations and wear-debris analysis, it is suggested that there exists a certain threshold for the amount and size of graphite particulates in these composites to enable them to have improved tribological properties. (Copyright (c) 1997 Elsevier Science B.V., Amsterdam. All rights reserved.)

  14. Research status of rare earth doped Mn-Zn ferrites synthesized by hydrothermal method%水热法制备稀土掺杂Mn-Zn铁氧体的研究现状

    Institute of Scientific and Technical Information of China (English)

    陈明洁; 庄琳; 沈辉

    2012-01-01

    The research status of Mn-Zn ferrites synthesized by hydrothermal method was summarized. The key factors of maintaining the initial stoichiometry and getting nanosized particles with narrow size distribution and perfect crystallization without impurity phase were discussed. Finally, according to the current research situation of rare earth doped Mn-Zn ferrite, the further research directions were proposed.%综述了水热法制备Mn-Zn铁氧体的研究现状,对制备出与初始化学计量一致、颗粒细小、尺寸分布窄且结晶程度好、没有杂相的纳米颗粒的关键合成条件进行了讨论.并针对目前的稀土掺杂Mn-Zn铁氧体微粉的研究现状,提出需要深入研究的几个方向.

  15. The morphology of carbon-metal composite synthesized in arc discharge

    Science.gov (United States)

    Smovzh, D. V.; Sakhapov, S. Z.; Zaikovskii, A. V.

    2016-10-01

    The phase state of nanoparticles and function of distribution by size of particles, formed at joint electric arc spraying of metal (Ni/Cu/Ti/Pt/Zr) - carbon electrode, is studied. It is shown that the metal and carbide nanoparticles with the size of 2-9 nm are formed in the carbon matrix at spraying. When annealing the metal-carbon composites, the metal-containing nanoparticles oxidize and coagulate, forming the agglomerates of 100 nm or more.

  16. Corrosion Properties in Sodium Chloride Solutions of Al–TiC Composites in situ Synthesized by HFIHF

    Directory of Open Access Journals (Sweden)

    El-Sayed M. Sherif

    2015-10-01

    Full Text Available Al–TiC nanocomposite materials have been prepared by a new in situ synthesizing technique. A mixture of aluminum, titanium, and graphite has been prepared using ball milling technique and then melted in a high frequency induction heat furnace (HFIHF at different sintering temperatures, namely 900, 1100, and 1300 °C. The effect of sintering temperature on the corrosion of the Al–TiC composite in 3.5% NaCl solutions was investigated using cyclic potentiodynamic polarization, chronoamperometric current-time, open-circuit potential, and electrochemical impedance spectroscopy measurements. The surface of the composites after their corrosion in the test solution was investigated using scanning electron microscopy and energy dispersive X-ray analyses. It has been found that all manufactured composites suffer uniform corrosion. All corrosion test techniques were consistent with each other and confirmed clearly that the corrosion resistance of Al composites increased according to their sintering temperature in the following order 900 > 1100 > 1300 °C.

  17. Removal of methylene blue from aqueous solution by a solvothermal-synthesized graphene/magnetite composite.

    Science.gov (United States)

    Ai, Lunhong; Zhang, Chunying; Chen, Zhonglan

    2011-09-15

    In this study, we have demonstrated a facile one-step solvothermal method for the synthesis of the graphene nanosheet (GNS)/magnetite (Fe(3)O(4)) composite. During the solvothermal treatment, in situ conversion of FeCl(3) to Fe(3)O(4) and simultaneous reduction of graphene oxide (GO) into graphene in ethylene glycol solution were achieved. Electron microscopy study suggests the Fe(3)O(4) spheres with a size of about 200 nm are uniformly distributed and firmly anchored on the wrinkled graphene layers with a high density. The resulting GNS/Fe(3)O(4) composite shows extraordinary adsorption capacity and fast adsorption rates for removal of organic dye, methylene blue (MB), in water. The adsorption kinetics, isotherms and thermodynamics were investigated in detail to reveal that the kinetics and equilibrium adsorptions are well-described by pseudo-second-order kinetic and Langmuir isotherm model, respectively. The thermodynamic parameters reveal that the adsorption process is spontaneous and endothermic in nature. This study shows that the as-prepared GNS/Fe(3)O(4) composite could be utilized as an efficient, magnetically separable adsorbent for the environmental cleanup.

  18. Prebiotic syntheses of vitamin coenzymes: II. Pantoic acid, pantothenic acid, and the composition of coenzyme A

    Science.gov (United States)

    Miller, S. L.; Schlesinger, G.

    1993-01-01

    Pantoic acid can by synthesized in good prebiotic yield from isobutyraldehyde or alpha-ketoisovaleric acid + H2CO + HCN. Isobutyraldehyde is the Strecker precursor to valine and alpha-ketoisovaleric acid is the valine transamination product. Mg2+ and Ca2+ as well as several transition metals are catalysts for the alpha-ketoisovaleric acid reaction. Pantothenic acid is produced from pantoyl lactone (easily formed from pantoic acid) and the relatively high concentrations of beta-alanine that would be formed on drying prebiotic amino acid mixtures. There is no selectivity for this reaction over glycine, alanine, or gamma-amino butyric acid. The components of coenzyme A are discussed in terms of ease of prebiotic formation and stability and are shown to be plausible choices, but many other compounds are possible. The gamma-OH of pantoic acid needs to be capped to prevent decomposition of pantothenic acid. These results suggest that coenzyme A function was important in the earliest metabolic pathways and that the coenzyme A precursor contained most of the components of the present coenzyme.

  19. Structure of bicomponent metal–oxide composites synthesized by electron beam irradiation method

    Energy Technology Data Exchange (ETDEWEB)

    Kugai, Junichiro, E-mail: kugai@mit.eng.osaka-u.ac.jp [Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Moriya, Toshiharu, E-mail: t-moriya@mit.eng.osaka-u.ac.jp [Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Seino, Satoshi, E-mail: seino@mit.eng.osaka-u.ac.jp [Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Nakagawa, Takashi, E-mail: nakagawa@mit.eng.osaka-u.ac.jp [Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Ohkubo, Yuji, E-mail: okubo@mit.eng.osaka-u.ac.jp [Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Ueno, Koji, E-mail: Kji_Ueno@EBIS.shi.co.jp [Japan Electron Beam Irradiation Service Co., 5-3 Odushima-cho Izumi-ohtsu, Osaka 595-0074 (Japan); Nitani, Hiroaki, E-mail: hiroaki.nitani@kek.jp [Institute of Materials Structure Science (IMSS), High Energy Accelerator Research Organization, 1-1 Oho, Tsukuba, Ibaraki 305-0801 (Japan); Yamamoto, Takao A., E-mail: takao@mit.eng.osaka-u.ac.jp [Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan)

    2013-11-15

    Highlights: •In radiation-induced process, transition metal precipitates only with Pt or support. •Reduced Cu atom stabilizes by forming Pt–Cu alloy or oxidatively depositing on CeO{sub 2}. •Sulfate stabilizes metals allowing their growth against oxidative deposition on CeO{sub 2}. •FeO{sub x} is directly formed without being reduced to metal due to its oxophilicity. •Fe{sup 3+} in the precursor inhibits reduction of Pt yielding highly oxidic Pt on support. -- Abstract: In order to understand the formation process of metal–oxide composite in an electron beam irradiation method in aqueous phase, the structure and composition of obtained solid were correlated to the synthesis parameters. Transition metal did not precipitate alone by the electron beam irradiation, but they did in the presence of platinum or support. Due to the relatively high reduction potential, copper underwent reduction to metallic state and readily precipitated by forming Pt–Cu alloy and/or copper oxide on solid surface. In the Pt–Cu/CeO{sub 2} system, the structure of Pt–Cu was ruled by two competing factors, growth of alloy nanoparticles promoted by sulfate ion and deposition of metal (alloy) on CeO{sub 2} support with their concomitant partial oxidation. CeO{sub 2} was suggested to immobilize the metals oxidatively before they coalesce. Iron barely formed alloy with Pt, but it directly precipitated on support as oxide without being reduced to metal due to its oxophilicity. Oxide was formed either via reduction to metallic state (for Pt and Cu) or through direct oxygenation or hydroxylation on solid (for Fe). Under the restriction of reduction potential, the size and composition of alloy nanoparticles and the content of oxide phase were drastically modified by support surface property and anion species in the solution.

  20. Hydrothermal Biogeochemistry

    Science.gov (United States)

    Shock, E.; Havig, J.; Windman, T.; Meyer-Dombard, D.; Michaud, A.; Hartnett, H.

    2006-12-01

    Life in hot spring ecosystems is confronted with diverse challenges, and the responses to those challenges have dynamic biogeochemical consequences over narrow spatial and temporal scales. Within meters along hot spring outflow channels at Yellowstone, temperatures drop from boiling, and the near-boiling conditions of hot chemolithotrophic communities, to those that permit photosynthesis and on down to conditions where nematodes and insects graze on the edges of photosynthetic mats. Many major and trace element concentrations change only mildly in the water that flows through the entire ecosystem, while concentrations of other dissolved constituents (oxygen, sulfide, ammonia, total organic carbon) increase or decrease dramatically. Concentrations of metals and micronutrients range from toxic to inadequate for enzyme synthesis depending on the choice of hot spring. Precipitation of minerals may provide continuous growth of microbial niches, while dissolution and turbulent flow sweeps them away. Consequently, microbial communities change at the meter scale, and even more abruptly at the photosynthetic fringe. Isotopic compositions of carbon and nitrogen in microbial biomass reflect dramatic and continuous changes in metabolic strategies throughout the system. Chemical energy sources that support chemolithotrophic communities can persist at abundant or useless levels, or change dramatically owing to microbial activity. The rate of temporal change depends on the selection of hot spring systems for study. Some have changed little since our studies began in 1999. Others have shifted by two or more units in pH over several years, with corresponding changes in other chemical constituents. Some go through daily or seasonal desiccation cycles, and still others exhibit pulses of changing temperature (up to 40°C) within minutes. Taken together, hydrothermal ecosystems provide highly manageable opportunities for testing how biogeochemical processes respond to the scale of

  1. Phase composition of SiC-ZrO2 composite materials synthesized from zircon doped La2O3

    Institute of Scientific and Technical Information of China (English)

    MA; Beiyue

    2009-01-01

    A study was carried out to determine the optimum parameters for synthesis of SiC-ZrO2 composite materials by carbothermal re-duction of zircon. Test samples were prepared by mixing average mesh size of less than 30 μm of carbon black and 40 μm of zircon with C/ZrSiO4 mass ratio of 0.2 and the extra addition amount of La2O3 was 0, 1 wt.% and 2 wt.%. Prepared samples were subjected to the car-bothermal reduction process at temperatures of 1723, 1753, 1773 and 1803 K for 4 h, respectively. The carbothermal reduction process was conducted in an atmosphere controlled tube furnace at an argon flow of 1.5 L/min. All products were examined by X-ray diffraction (XRD) to determine the transformation. The results showed that the best transformation of SiC-ZrO2 composite materials occurred at 1803 K for 4 h with the amount of 2 wt.%La2O3.

  2. A novel organic-inorganic hybrid composition for controllably synthesizing AgI nanocrystals

    Science.gov (United States)

    Liu, Junxue; He, Sheng; An, Changhua; Zhang, Jun

    2017-05-01

    The ability to control the shape and morphology of semiconductor macro/nanocrystals is critical to applications such as photocatalysis, electrocatalysis, photonics and nanoelectronics. Despite significant advances in controlling the shapes by thermal decomposition and solvothermal methods, rigorous shape control by low temperature and aqueous phase controlling remains challenging. Herein, a facile synthetic method based on ethylenediamine assisted precursor transformation technique has been developed for the fabrication of AgI nanocrystals. The central features of our approach are the use of ethylenediamine (en) as complexant and the use of polyvinylpyrrolidone (PVP) as capping surfactants to form Ag(en)xI precursor, which is followed by removing en to form AgI crystals. This work provides new insights into the use of a novel organic-inorganic hybrid composition as precursors for nanocrystals synthesis and offers a potential route to achieve well-defined morphology of inorganic nanostructures with uniform shape and size.

  3. Synthesizing the Y-123/Y-211 composite by the PVA method

    Energy Technology Data Exchange (ETDEWEB)

    Serradilla, I.G; Capdevila, X.G.; Espiell, F. [Departament d' Enginyeria Quimica i Metallurgia, Facultat de Quimica, Universitat de Barcelona (Spain); Calleja, A; Segarra, M. [DIOPMA, S.L., Barcelona (Spain); Mendoza, E.; Teva, J.; Granados, X.; Obradors, X. [Institut de Ciencia de Materials de Barcelona-CSIC, Campus de la UAB, Bellaterra (Spain)

    2002-04-01

    A polymerized organic-inorganic synthesis of a mixture containing 69% Y-123, 30% Y-211, 1% CeO{sub 2} in weight has been studied with the aid of polyvinylic alcohol (PVA). The advantages of this method are (a) avoidance of extensive and repetitive firing steps and (b) no need for mechanical mixing of components. By heating the solution of stoichiometric quantities of the nitrate salts, a viscous gel is obtained which turns into an aerogel by subsequent heating. The resulting aerogel was calcined in a single step and the powder was used to prepare Y-123/Y-211 composite monodomain rods by the vertical Bridgman solidification technique. Characterization of both powders and grown monodomains have been performed. Fine and dispersed Y-211 phase distribution was successfully achieved. Finally, magnetic measurements were performed by SQUID magnetometry. (author)

  4. Improvement of photofatigue resistance of spirooxazine entrapped in organic-inorganic composite synthesized via the sol-gel process

    Science.gov (United States)

    Hou, Lisong; Mennig, Martin; Schmidt, Helmut K.

    1994-10-01

    A photochromic dye, spirooxazine (SO), was incorporated in organic-inorganic composite (OIC) materials by the advantages of sol-gel processing. It has been found that the photochromic response is high enough and the fading rate is similar to the dye-in-ethanol solution while the photofatigue resistance is strongly dependent on the matrix composition and the starting compounds. In the present work, we present results on the effect of matrix composition and starting compounds as well as additives on the photofatigue resistance of SO- OIC photochromic coatings. Sol-gel coatings synthesized from methyltrimethoxysilane (MTMS) and glycidyloxypropyltrimethoxysilane (GPTMS) as starting compounds, and using 1H,1H,2H,2H-perfluoroalkyltrimethoxysilane (FAS) and 1-methylimidazole (MI) as additives provide the SO dye with a favorable matrix environment in terms of photofatigue, so that the overall photochromic performance of the dye can be optimized. The photofatigue resistance reaches the same level as, while both the photochromic response and fading rate are much better than the SO-PMMA coatings.

  5. Assembly and electroanalytical performance of Prussian blue/polypyrrole composite nanoparticles synthesized by the reverse micelle method

    Energy Technology Data Exchange (ETDEWEB)

    Miao Yuqing; Liu Jiwei, E-mail: biosensors@zjnu.c [Laboratory of Biocatalysis and Biosensor, Institute of Physical Chemistry, Zhejiang Normal University, Jinhua 321004 (China)

    2009-04-15

    We report on the characterization, assembly and electroanalytical performance of Prussian blue/polypyrrole (PBPPy) composite nanoparticles synthesized by the reverse micelle method. Scanning electron microscopy suggests the formation of nanosized PBPPy particles with diameters between 40 and 50 nm. Optical absorption confirms that the particles are composed of Prussian blue (PB) and polypyrrole. PB and PBPPy nanoparticles were anchored onto the surface of cysteine-modified Au electrodes. Cyclic voltammetry experiments show that PB- or PBPPy-modified electrodes exhibit intrinsic electrochemical properties and a high electrocatalytic activity towards H{sub 2}O{sub 2}. PBPPy-modified electrodes exhibit a higher sensitivity to H{sub 2}O{sub 2} than PB-modified electrodes. A linear calibration curve in the concentration range 0.99 {mu}M-8.26 mM H{sub 2}O{sub 2} is constructed with a detection limit of 0.23 {mu}M at a signal-to-noise ratio of 3. Excellent stability is observed for PBPPy-composite-nanoparticle-modified electrodes even in a pH 6 phosphate buffer solution with a high H{sub 2}O{sub 2} concentration (0.99 mM). Glutaraldehyde and Nafion were also employed to immobilize glucose oxidase for the development of PBPPy-based biosensors. The results show that PBPPy composite nanoparticles can be used to develop oxidase-based biosensors.

  6. Assembly and electroanalytical performance of Prussian blue/polypyrrole composite nanoparticles synthesized by the reverse micelle method.

    Science.gov (United States)

    Miao, Yuqing; Liu, Jiwei

    2009-04-01

    We report on the characterization, assembly and electroanalytical performance of Prussian blue/polypyrrole (PBPPy) composite nanoparticles synthesized by the reverse micelle method. Scanning electron microscopy suggests the formation of nanosized PBPPy particles with diameters between 40 and 50 nm. Optical absorption confirms that the particles are composed of Prussian blue (PB) and polypyrrole. PB and PBPPy nanoparticles were anchored onto the surface of cysteine-modified Au electrodes. Cyclic voltammetry experiments show that PB- or PBPPy-modified electrodes exhibit intrinsic electrochemical properties and a high electrocatalytic activity towards H2O2. PBPPy-modified electrodes exhibit a higher sensitivity to H2O2 than PB-modified electrodes. A linear calibration curve in the concentration range 0.99 μM-8.26 mM H2O2 is constructed with a detection limit of 0.23 μM at a signal-to-noise ratio of 3. Excellent stability is observed for PBPPy-composite-nanoparticle-modified electrodes even in a pH 6 phosphate buffer solution with a high H2O2 concentration (0.99 mM). Glutaraldehyde and [Formula: see text] were also employed to immobilize glucose oxidase for the development of PBPPy-based biosensors. The results show that PBPPy composite nanoparticles can be used to develop oxidase-based biosensors.

  7. Assembly and electroanalytical performance of Prussian blue/polypyrrole composite nanoparticles synthesized by the reverse micelle method

    Directory of Open Access Journals (Sweden)

    Yuqing Miao and Jiwei Liu

    2009-01-01

    Full Text Available We report on the characterization, assembly and electroanalytical performance of Prussian blue/polypyrrole (PBPPy composite nanoparticles synthesized by the reverse micelle method. Scanning electron microscopy suggests the formation of nanosized PBPPy particles with diameters between 40 and 50 nm. Optical absorption confirms that the particles are composed of Prussian blue (PB and polypyrrole. PB and PBPPy nanoparticles were anchored onto the surface of cysteine-modified Au electrodes. Cyclic voltammetry experiments show that PB- or PBPPy-modified electrodes exhibit intrinsic electrochemical properties and a high electrocatalytic activity towards H2O2. PBPPy-modified electrodes exhibit a higher sensitivity to H2O2 than PB-modified electrodes. A linear calibration curve in the concentration range 0.99 μM–8.26 mM H2O2 is constructed with a detection limit of 0.23 μM at a signal-to-noise ratio of 3. Excellent stability is observed for PBPPy-composite-nanoparticle-modified electrodes even in a pH 6 phosphate buffer solution with a high H2O2 concentration (0.99 mM. Glutaraldehyde and { m Nafion}^{iny{extregistered}} were also employed to immobilize glucose oxidase for the development of PBPPy-based biosensors. The results show that PBPPy composite nanoparticles can be used to develop oxidase-based biosensors

  8. Composite titanium nitride layers produced on the AZ91D magnesium alloy by a hybrid method including hydrothermal modification of the layer

    Science.gov (United States)

    Tacikowski, M.; Grzonka, J.; Płociński, T.; Jakieła, R.; Pisarek, M.; Wierzchoń, T.

    2015-08-01

    The microstructure and properties of the composite TiN-Ti-Al type titanium nitride surface layer with a sub-layer of titanium and aluminium produced on AZ91D magnesium alloy using a hybrid PVD method including final sealing by hydrothermal treatment were investigated. The results were analysed in terms of the microstructure-properties correlation, to approach the role of the sub-layers and the mechanisms involved in the properties improvement. The microstructure investigations indicate that the composite titanium nitride layers are tight and have nano-crystalline, diffusive character and multi zone microstructure of the type TixOy-TiN-Ti-Al-Al3Mg2-Al12Mg17. The significant corrosion resistance improvement of the AZ91D alloy obtained using the sealed composite titanium nitride layers was found to be the result of a synergistic mechanism which combined hydrothermal treatment of the layer with an action of aluminium sub-layer which is critical to make the sealing effective. The diffusive bonding via Mg-Al zone improves adhesion and the load bearing capacity of titanium nitride layers in wear conditions.

  9. Preparation of nanocrystalline composite TiO2-SnO2 powders using sol-gel method combined with hydrothermal treatment

    Directory of Open Access Journals (Sweden)

    Anna Marzec

    2016-12-01

    Full Text Available The paper describes the process of TiO2-SnO2 nanocomposites manufacturing utilizing two-step sol-gel method combined with calcination (in the case of titanium hydroxide gel or hydrothermal treatment (in the case of tin hydroxide. Phase composition of the obtained nanopowders and average crystallite sizes were determined using XRD analysis. Measurements of the specific surface area were performed using sorption method based on determination of physical adsorption isotherm (BET. Morphology of the nanopowders was observed using transmission electron microscope. The presented synthesis method enables to obtain composites nanopowders from TiO2-SnO2 system with known and controlled chemical and phase compositions, and distinctly diversified TiO2 and SnO2 particle sizes.

  10. Formation and composition of titanium oxinitride nanocrystals synthesized via nitridizing titanium oxide for nonvolatile memory applications

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Li-Wei; Chang, Chun-Yen [Department of Electronics Engineering, National Chiao Tung University, Hsinchu, 300, Taiwan (China); Institute of Electronics, National Chiao Tung University, Hsinchu, 300, Taiwan (China); Chang, Ting-Chang, E-mail: tcchang@mail.phys.nsysu.edu.tw [Department of Physics, National Sun Yat-Sen University, Kaohsiung, 804, Taiwan (China); Center for Nanoscience and Nanotechnology, National Sun Yat-Sen University, Kaohsiung, 804, Taiwan (China); Tu, Chun-Hao; Wang, Pai-Syuan [Department of Electronics Engineering, National Chiao Tung University, Hsinchu, 300, Taiwan (China); Institute of Electronics, National Chiao Tung University, Hsinchu, 300, Taiwan (China); Lin, Chao-Cheng [Green Energy and Environment Research Laboratories, Industrial Technology Research Institute, Hsinchu, 310, Taiwan (China); Chen, Min-Chen [Department of Physics, National Sun Yat-Sen University, Kaohsiung, 804, Taiwan (China); Huang, Hui-Chun; Gan, Der-Shin; Ho, New-Jin [Institute of Materials Science and Engineering, National Sun Yat-Sen University, Kaohsiung, 804, Taiwan (China); Chen, Shih-Ching [Department of Physics, National Sun Yat-Sen University, Kaohsiung, 804, Taiwan (China); Chen, Shih-Cheng [Department of Electrical Engineering, National Tsing Hua University, Hsinchu, 310, Taiwan, ROC (China); Institute of Electronic Engineering, National Tsing Hua University, Hsinchu, 310, Taiwan (China)

    2011-09-01

    Formation and composition analyses of titanium oxinitride nanocrystals (NCs) fabricated via treating a magnetron co-sputtered thin film of titanium and silicon dioxide with a rapid thermal annealing in nitrogen ambient were demonstrated for nonvolatile memory applications. Phase separation characteristics with different annealing conditions were examined by transmission electron microscopy and chemical bonding characteristics were confirmed by X-ray photon emission spectra. It was observed that a blanket layer composed mainly of titanium oxide was still present as annealing temperature was increased to 700 deg. C, associated with the thermodynamically stable phase of titanium oxide. Furthermore, a higher thermal treatment of 900 deg. C induced formation of a well-separated NC structure and caused simultaneously partial nitridation of the titanium oxide, thereby forming titanium oxinitride NCs. A significant capacitance-voltage hysteresis in threshold voltage shift at 1 V was easily achieved under a small sweeping voltage range of + 2 V/-2 V, and a memory window retention of 2.2 V was obtained after 10{sup 7} s by extrapolation under a 1 s initial-program/erase condition of + 5 V/-5 V, respectively.

  11. Morphological characterization of LiFePO{sub 4}/C composite cathode materials synthesized via a carboxylic acid route

    Energy Technology Data Exchange (ETDEWEB)

    Fey, George Ting-Kuo; Lu, Tung-Lin [Department of Chemical and Materials Engineering, National Central University, Chung-Li 32054 (China)

    2008-04-01

    A new type of LiFePO{sub 4}/C composite surrounded by a web containing both amorphous and crystalline carbon phases was synthesized by incorporating malonic acid as a carbon source using a high temperature solid-state method. SEM, TEM/SAED/EDS and HRTEM were used to analyze surface morphology and confirmed for the first time that crystalline carbon was present in LiFePO{sub 4}/C composites. The composite was effective in enhancing the electrochemical properties such as capacity and rate capability, because its active component consists of nanometer-sized particles containing pores with a wide range of sizes. An EDS elemental map showed that carbon was uniformly distributed on the surface of the composite crystalline particles. TEM/EDS results clearly show a dark region that is LiFePO{sub 4} with a trace of carbon and a gray region that is carbon only. To evaluate the materials' electrochemical properties, galvanostatic cycling and conductivity measurements were performed. The best cell performance was delivered by the material coated with 60 wt.% malonic acid, which delivered first cycle discharge capacity of 149 mAh g{sup -1} at a C/5 rate and sustained 222 cycles at 80% of capacity retention. When carboxylic acid was used as a carbon source to produce LiFePO{sub 4}, overall conductivity increased from 10{sup -5} to 10{sup -4} S cm{sup -1}, since particle growth was prevented during the final sintering process. (author)

  12. Antimicrobial activity and biocompatibility of Ag{sup +}- and Cu{sup 2+}-doped biphasic hydroxyapatite/α-tricalcium phosphate obtained from hydrothermally synthesized Ag{sup +}- and Cu{sup 2+}-doped hydroxyapatite

    Energy Technology Data Exchange (ETDEWEB)

    Radovanović, Željko, E-mail: zradovanovic@tmf.bg.ac.rs [Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11000 Belgrade (Serbia); Jokić, Bojan; Veljović, Djordje; Dimitrijević, Suzana [Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11000 Belgrade (Serbia); Kojić, Vesna [Oncology Institute of Vojvodina, Institutski put 4, 21204 Sremska Kamenica (Serbia); Petrović, Rada; Janaćković, Djordje [Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11000 Belgrade (Serbia)

    2014-07-01

    Hydroxyapatite (HAp) powders doped with Ag{sup +} or Cu{sup 2+} were synthesized by a hydrothermal method in order to obtain biomaterial with an antimicrobial effect. The synthesis was performed with two contents of dopant (Ag{sup +} or Cu{sup 2+}) by considering both the antimicrobial activities and biocompatibility of the powders. The doped HAp was annealed at 1200 °C for 2 h with the intention of investigating the influence of doping with Ag{sup +} and Cu{sup 2+} on the creation of the biphasic HAp/α-tricalcium phosphate (HAp/α-TCP) and determining the antimicrobial activity and biocompatibility of the obtained biphasic powders. Analyses of all powders, undoped and doped HAp and HAp/α-TCP, were performed by Field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), atomic absorption spectroscopy (AAS) and energy-dispersive X-ray spectroscopy (EDS). The in vitro antibacterial activities of the powders were evaluated against: Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa and Candida albicans. All powders showed good antimicrobial activity but generally the powders of doped HAp/α-TCP had more uniform results against all pathogenic microorganisms than the powders of doped HAp. In vitro biocompatibility tests, MTT and DET, were used to evaluate the biocompatibility of Ag{sup +}- and Cu{sup 2+}-doped HAp/α-TCP with MRC-5 human fibroblast cells. These tests confirmed that powders do not have a cytotoxic effect. The HAp/α-TCP powders doped with the lower content of Ag{sup +} and Cu{sup 2+} showed especially good biocompatibility. Antimicrobial and biocompatibility tests recommend the Ag{sup +}- and Cu{sup 2+}-doped HAp/α-TCP as promising material for use in reconstructive surgery of bone.

  13. Thermal−Electrical Character of in Situ Synthesized Polyimide-Grafted Carbon Nanofiber Composites

    Energy Technology Data Exchange (ETDEWEB)

    Arlen, Michael J.; Wang, David; Jacobs, J. David; Justice, Ryan; Trionfi, Aaron; Hsu, Julia W.P.; Schaffer, Dale; Tan, Loon-Seng; Vaia, Richard A. (Sandia); (UCIN); (AFRL)

    2008-12-09

    Notwithstanding the success of polymer-carbon nanotube (CNT) nanocomposites, a solid understanding of the impact of external perturbations, including temperature and stress, on the electrical response, its reproducibility, and the subsequent relationship to the topology of the percolative morphology and molecular details of the CNT-CNT contact junction is not complete. Using an in situ synthesis approach, two series of polymide (CP2)-carbon nanofiber (CNF) composites are prepared with quantitatively (small-angle X-ray scattering) comparable CNF dispersions, but differing in the structure of the CNF-polymer interface. Amino-functionalized CNFs (FCNFs) enable direct formation of CP2 grafts onto the CNFs, whereas pristine CNFs (PCNFs) result in a relatively weak interface between the carbon nanofiber and CP2 matrix. In general, low-frequency ac impedance measurements are well described by the percolation bond model, yielding a percolation threshold below 1 vol % (0.24 and 0.68 vol % for PCNF-CP2 and FCNF-CP2, respectively). However, the design of the interface is determined to be crucial for controlling the electrical behavior in four substantial ways: magnitude of the limiting conductivity, linearity of the I-V response, magnitude and direction of temperature-dependent resistivity, and reproducibility of the absolute value of the resistivity with thermal cycling. These observations are consistent with a direct CNF-CNF contact limiting transport in the PCNF-CP2 system, where the CP2 grafts onto the FCNF from a dielectric layer, limiting transport within the FCNF-CP2 system. Furthermore, the grafted CP2 chains on the FCNF reduce local polymer dewetting at the CNF surfaces when the temperature exceeds the CP2 glass transition. This appears to stabilize the structure of the percolation network and associated conductivity. The general behavior of these interfacial extremes (pristine and fully functionalized CNFs) set important bounds on the design of interface

  14. Major element compositions of fluid inclusions from hydrothermal vein-type deposits record eroded sedimentary units in the Schwarzwald district, SW Germany

    Science.gov (United States)

    Walter, Benjamin F.; Burisch, Mathias; Marks, Michael A. W.; Markl, Gregor

    2017-02-01

    Mixing of sedimentary formation fluids with basement-derived brines is an important mechanism for the formation of hydrothermal veins. We focus on the sources of the sediment-derived fluid component in ore-forming processes and present a comprehensive fluid inclusion study on 84 Jurassic hydrothermal veins from the Schwarzwald mining district (SW Germany). Our data derive from about 2300 fluid inclusions and reveal differences in the average fluid composition between the northern, central, and southern Schwarzwald. Fluids from the northern and southern Schwarzwald are characterised by high salinities (18-26 wt% NaCl+CaCl2), low Ca/(Ca+Na) mole ratios (0.1-0.4), and variable Cl/Br mass ratios (30-1140). In contrast, fluids from the central Schwarzwald show even higher salinities (23-27 wt% NaCl+CaCl2), higher Ca/(Ca+Na) mole ratios (0.2-0.9), and less variable Cl/Br mass ratios (40-130). These fluid compositions correlate with the nature and thickness of the now eroded sedimentary cover rocks. Compared to the northern and the southern Schwarzwald, where halite precipitation occurred during the Middle Triassic, the sedimentary basin in the central Schwarzwald was relatively shallow at this time and no halite was precipitated. Accordingly, Cl/Br ratios of fluids from the central Schwarzwald provide no evidence for the reaction of a sedimentary brine with halite, whereas those from the northern and southern Schwarzwald do. Instead, elevated Ca/(Ca+Na), high SO4 contents, and relatively low Cl/Br imply the presence of a gypsum dissolution brine during vein formation in the central Schwarzwald which agrees with the reconstructed regional Triassic geology. Hence, the information archived in fluid inclusions from hydrothermal veins in the crystalline basement has the potential for reconstructing sedimentary rocks in the former overburden.

  15. C-LFP-multi-walled carbon nanotubes composite cathode materials synthesized by solid-state reaction for lithium ion batteries.

    Science.gov (United States)

    Hwang, Yun-Hwa; Prabakar, S J Richard; Pyo, Myoungho

    2013-08-01

    Multi-walled carbon nanotubes (MWNT) was utilized as a conductive additive to enhance the capacity and rate capability of carbon coated LiFePO4 (C-LFP). Composites of C-LFP with MWNT (C-LFP-MWNT) were prepared by blending MWNT at different stages of C-LFP synthesis. The pre-blending (PrB) of MWNT (5, 10, 15 wt%) with LFP precursor (PrB-C-LFP-MWNT) before calcination in a reducing environment (5 vol% H2 in N2) at 750 degrees C, produced phase pure crystalline LFP with a reduction in particle size as increase in MWNT content. This was contrasted with post-blending (PoB) of MWNT with as-synthesized C-LFP (PoB-C-LFP-MWNT), which gave inferior electrochemical performances. The PrB-C-LFP-MWNT (10 wt%) composite showed better cycle stability, higher rate capability, and faster Li diffusion characteristics than PoB-C-LFP-MWNT.

  16. The Phase-Formation Behavior of Composite Ceramic Powders Synthesized by Utilizing Rice Husk Ash from the Biomass Cogeneration Plant

    Directory of Open Access Journals (Sweden)

    Wenjie Yuan

    2015-01-01

    Full Text Available The development and utilization of biomass as a vital source of renewable energy were stimulated in order to reduce the global dependency on fossil fuels. A lot of rice husk ashes (RHA were generated as the waste after the rice husk as the main fuel was burnt in the biomass cogeneration plant. The phase-formation behavior of composite ceramic powders synthesized by using rice husk ash from the biomass cogeneration plant at the different carbon ratios and temperatures was investigated. The sequence of phase formation with the calcining temperatures ranging from 1773 K to 1853 K was followed by O′-Sialon→SiC + Si3N4→SiC in samples with C/SiO2  =  1 : 1–4 : 1. Ca-α-Sialon formed in samples with C/SiO2  =  5 : 1 and 6 : 1. The results highlighted that series of reactions happening sensitively depended on C/SiO2 and the temperature and demonstrated that the carbothermal nitridation provided an alternative for converting RHA waste into composite ceramic powders.

  17. Microstructure and Mechanical Properties of In-situ Synthesized Al2O3/TiAl Composites

    Institute of Scientific and Technical Information of China (English)

    Ai Taotao

    2008-01-01

    Al2O3 particle-reinforced TiAI composites are successfully reaction-synthesized from the powder mixture of Ti, A1, TiO2, and Nb2O5, using the hot pressing reaction synthesis technique. The microstmcture and mechanical properties of the as-sintered products are investigated. It is found that in the as-sintered products consisting of γ-TiA1, α2-Ti3Al, Al2O3, and NbAl3 phases, the f'me Al2O3 particles tend to disperse on the grain boundaries. With the Nb2O5 content increasing, the grains are remarkably refined and the Al2O3 particles are dispersing more uniformly in the TiAI matrix, forming a partial lamellar structure containing γ and lamellar phases. The hardness of the in-situ composites increases gradually, and the bending strength and the fi-acture toughness of the as-sintered products reach the maxi-

  18. Helium,neon and argon isotope compositions of fluid inclu-sions in massive sulfides from the Jade hydrothermal field,the Okinawa Trough

    Institute of Scientific and Technical Information of China (English)

    ZENG Zhigang; QIN Yunshan; ZHAI Shikui

    2004-01-01

    Helium, neon and argon isotope compositions of fluid inclusions have been measured in massive sulfide samples from the Jade hydrothermal field in the central Okinawa Trough. Huid-inclusion 3He/4He ratios are between 6.2 and 10.1 times the air value (Ra), and with a mean of 7.8Ra, which are consistent with the mid-ocean ridge basalt values [3He/4He≈(6Ra~11Ra)]. Values for 20Ne/22Ne are from 10.7 to 11.3, which are significantly higher than the atmospheric ratio (9.8).And the fluid-inclusion 40Ar/36Ar ratios range from 287 to 334, which are close to the atmosperic values (295.5). These results indicate that the noble gases of trapped hydrothermal fluids in massive sulfides are a mixture of mantle- and seawater-derived components, and the helium of fluid inclusions is mainly from mantle, the nelium and argon isotope compositions are mainly from seawater.

  19. Microbiological production and ecological flux of northwestern subduction hydrothermal systems

    Science.gov (United States)

    Sunamura, M.; Okamura, K.; Noguchi, T.; Yamamoto, H.; Fukuba, T.; Yanagawa, K.

    2012-12-01

    Deep-sea hydrothermal system is one of the most important sources for heat and chemical flux from the oceanic crust to the global ocean. The rich biological community around the hydrothermal vent shows chemolithoautotrophic microbial production are important in deep sea ecosystems. More than 99% of microbiological available chemical components in hydrothermal vent fluid, e.g. sulfide, methane, hydrogen, Fe2+, and Mn2+, is released into surrounding seawater to construct hydrothermal plume, suggesting that the chemolithoautotrophic-microbial primary production in the hydrothermal plume is huge and important in the whole hydrothermal ecosystems. To understand the impact of hydrothermal plume to a microbial ecosystem and a connectivity with zooplankton, we targeted and investigated a total of 16 hydrothermal fileds (7 sites in Okinawa trough, 3 sites in Ogasawara arc, and 6 sites in Mariana arc and back arc) and investigated in several cruises under the TAIGA project in Japan. Hydrothermal fluids in the subduction system are rich in sulfide. The hydrothermal fluids in the Okinawa trough, Ogasawara arc. and Mariana trough are characterized by rich in methane, poor in other reduced chemicals, and rich in iron, respectively. The major microbial composition was a potential sulfur oxidizing microbes SUP05 in the plume ecosystems, while an aerobic methanotrophic bacteria was secondary major member in methane-rich hydrothermal systems in Okinawa trough. Microbial quantitative and spatial distribution analyses of each plume site showed that the microbial population size and community structures are influenced by original chemical components of hydrothermal fluid, e.g. sulfide, methane and iron concentration. Microbial quantitative data indicated the removal/sedimentation of microbial cells from the plume and effect of phase separation in a same vent field through construction of gas-rich or gas-poor plumes. After the correlation of plume mixing effect, we estimates that the

  20. One-Step Hydrothermal Preparation and Electrochemical Performance of Graphene/Sulfur Cathode Composites%石墨烯/硫复合正极材料的一步水热法制备与电化学性能

    Institute of Scientific and Technical Information of China (English)

    李庆洲; 李玉惠; 李亚娟; 刘又年

    2014-01-01

    将硫代硫酸钠(Na2S2O3)与氧化石墨烯(GO)的混合溶液,在酸性条件下经过一步水热反应制备还原氧化石墨烯/硫(RGO/S)复合正极材料.实验探索了水热温度、反应时间、碳硫质量比例对材料的影响.通过X射线衍射(XRD)、扫描电镜(SEM)、透射电镜(TEM)和恒电流充放电对材料进行分析.结果表明在180°C下,碳硫质量比为3:7时,水热12 h得到的RGO/S复合材料具有优异的循环性能,首次放电比容量为931 mAh∙g-1,50次循环之后其比容量还保持在828.16 mAh∙g-1;RGO/S复合材料的充放电库仑效率在95%以上;同时RGO/S复合材料的倍率性能相比于单质硫有很大提高.一步水热法能够使硫分子均匀分布在石墨烯片层结构中,同时加强了石墨烯表面基团对硫分子的固定作用.%Reduced graphene oxide/sulfur (RGO/S) composites were synthesized by a one-step hydrothermal method using a mixture of sodium thiosulfate (Na2S2O3) and graphene oxide (GO) solution reacting under acid conditions. We explored the influence of the hydrothermal temperature, reaction time, and sulfur content on the composites. Analysis by X-ray diffraction (XRD), scanning electron microscope (SEM), and the galvanostatic charge and discharge shows that the composites have excellent cycling performance when synthesis occurs at 180 °C for 12 h to provide a carbon:sulfur mass ratio of 3:7. The first discharge capacity is delivered at 931 mAh∙g-1 and it remains at 828.16 mAh∙g-1 after 50 cycles. The coulomb efficiency of the composites is above 95%. In addition, the rate capability of these composites is much better than that of sulfur. Sulfur molecules can be evenly distributed between the graphene layers and fixed to the functional groups on the surface of graphene by this one-step hydrothermal method.

  1. Physical and Gas Permeation Properties of a Series of Novel Hybrid Inorganic-Organic Composites Based on a Synthesized Fluorinated Polyimide

    OpenAIRE

    2000-01-01

    A series of hybrid inorganic-organic composites were fabricated from a functionalized fluorinated polyimide and tetraethoxysilane (TEOS), tetramethoxysilane, methyltrimethoxysilane (MTMOS), and phenyltrimethoxy-silane (PTMOS) employing the sol-gel process. Polyimides were synthesized from 4,4'-hexafluoroisopropylidene dianiline (6FpDA) and 4,4'-hexafluoroisopropyl-idenediphthalic anhydride (6FDA) utilizing a solution imidization technique. The hybrid materials were synthesized by in-situ so...

  2. Comparison of Kinetic Study of CTMA+ Removal of Molecular Sieve Ti-MCM-41 Synthesized with Natural and Commercial Silica

    OpenAIRE

    Fontes,Maria do Socorro Braga; Melo,Dulce Maria de Araújo; Costa,Cintia de Castro; Braga,Renata Martins; Melo,Marcus Antonio de Freitas; Alves,José Antônio Barros Leal Reis

    2015-01-01

    This work aimed to determine and compare the apparent activation energy, involved in thermal decomposition of CTMA+ from the pores of Ti-MCM-41 synthesized by two different source of silica in order to evaluate their influence in the template removal. The molecular sieves Ti-MCM-41 were synthesized using rice husk ash (RHA), as alternative low cost source of silica, and commercial silica gel, obtaining two mesoporous material by hydrothermal synthesis of gel molar composition of: 1.0 CTMABr: ...

  3. Strong bonding strength between HA and (NH4)2S2O8-treated carbon/carbon composite by hydrothermal treatment and induction heating.

    Science.gov (United States)

    Xiong, Xin-bo; Zeng, Xie-rong; Zou, Chun-li; Zhou, Ji-Zhao

    2009-06-01

    Carbon/carbon composite with hydroxyapatite (HA) coating is an attractive material in the dental and orthopedic fields, but the reported bonding strength between them was very poor. In this study, a compact crystalline HA coating on (NH(4))(2)S(2)O(8)-treated C/C substrate about 10 microm in width was obtained by hydrothermal treatment and induction heating. The microstructure, composition and morphologies of the as-prepared coatings were identified by X-ray diffraction, scanning electron microscopy and energy dispersive spectroscopy. A strong shear strength averaging 74.2 MPa between C/C substrate and HA was achieved and adhesion failures were observed more frequently than cohesion failures. The coating adhesion measured using a scratch test was 23 N and the reasons for this are discussed.

  4. Effect of Hydrothermal Treatment on Phase Composition of Titanium Dioxide Obtained by Ti(OC4H94 Hydrolysis

    Directory of Open Access Journals (Sweden)

    M.G. Mizilevska

    2015-03-01

    Full Text Available The use of hydrothermal treatment of amorphous material obtained by hydrolysis of titanium tetra-butoxide provides a nanostructured mixture of anatase and brookite – photocatalytic active phases of titanium dioxide, which are characterized by resistance to temperature phase transition in rutile if particle size is about 4 nm and value of the specific surface area is 175 m2/g.

  5. Hydrothermal synthesis of hydroxyapatite

    Science.gov (United States)

    Earl, J. S.; Wood, D. J.; Milne, S. J.

    2006-02-01

    A hydrothermal method of synthesizing hydroxyapatite by heating a precipitate, formed by mixing Ca(NO3)2bold dot4H2O and (NH4)2HPO4 with distilled water, in a hydrothermal reactor at 200 °C for 24-72 hrs is described. A treatment time of 24 hrs produced single phase (as shown by XRD) hydroxyapatite powder, however for longer treatment times XRD patterns were indicative of the presence of a secondary phase, monetite (CaHPO4). SEM examination of the treated powders displayed particles of rod-like morphology with dimensions 100-500 nm in length and 10-60 nm in diameter. Preliminary results on the use of the particles for the infiltration of dentine tubules are presented.

  6. Hydrothermal synthesis of hydroxyapatite

    Energy Technology Data Exchange (ETDEWEB)

    Earl, J S; Wood, D J; Milne, S J [Institute for Materials Research, University of Leeds, Leeds, LS2 9JT (United Kingdom)

    2006-02-22

    A hydrothermal method of synthesizing hydroxyapatite by heating a precipitate, formed by mixing Ca(NO{sub 3}){sub 2}{center_dot}4H{sub 2}O and (NH{sub 4}){sub 2}HPO{sub 4} with distilled water, in a hydrothermal reactor at 200 deg. C for 24-72 hrs is described. A treatment time of 24 hrs produced single phase (as shown by XRD) hydroxyapatite powder, however for longer treatment times XRD patterns were indicative of the presence of a secondary phase, monetite (CaHPO{sub 4}). SEM examination of the treated powders displayed particles of rod-like morphology with dimensions 100-500 nm in length and 10-60 nm in diameter. Preliminary results on the use of the particles for the infiltration of dentine tubules are presented.

  7. Hydrothermal synthesis of graphene-LaFeO3 composite supported with Cu-Co nanocatalyst for higher alcohol synthesis from syngas

    Science.gov (United States)

    Niu, T.; Liu, G. L.; Chen, Y.; Yang, J.; Wu, Jiang; Cao, Y.; Liu, Y.

    2016-02-01

    The composite of graphene and a perovskite-type oxide (PTO) should be an attractive new material, owing to the special properties of graphene and the flexibility of PTO. Both graphene and PTO are promising support for some metallic nanoparticles. Therefore, in this work, taking LaFeO3 as the representative for PTO, a novel composite of graphene sheets-LaFeO3 has been prepared by using hydrothermal synthesis, and bimetallic nanoparticles of Cu-Co have been loaded on the composite. The resultant catalyst is applied to higher alcohols synthesis (HAS) from syngas. The morphology, structure and the state of the bimetallic composite catalyst are characterized by using techniques of SEM, TEM, AFM, XRD, TPR, Raman and N2 adsorption-desorption. For the graphene-LaFeO3 support, the graphene sheets are embedded into the bulk LaFeO3 or uniformly deposited on the surface of the LaFeO3 grains, resulting in high specific surface area. And the mass transferring ability of the bimetallic catalyst is optimized by uniform mixing of graphene and LaFeO3 and the formation of the mesopores. For the active component, the Cu-Co alloy nanoparticles are highly dispersed on the graphene-LaFeO3 composite, which leads to the high activity, high selectivity and excellent stability to higher alcohols.

  8. 八角微米结构CuO的水热法合成及其光吸收特性%Star Anise-microstructured CuO Synthesized via the Hydrothermal Method and Their Optical Absorption Properties

    Institute of Scientific and Technical Information of China (English)

    傅小明; 潘卫军

    2013-01-01

    Sar anise-microstructured CuO is successfully synthesized with 1m mol CuCl2 as copper source and 1 m mol Na2CO3 as auxiliary salt at 240 ℃ for 48 h via the simple hydrothermal method.The phase,the morphologies and the optical absorption property of the samples have been characterized by X-ray diffraction (XRD),scanning electron microscope (SEM) and ultraviolet-visible absorption spectroscopy (UV-VIS),respectively.XRD analysis shows that the phase of as-obtained samples is CuO.SEM analysis confirms that the increasement of the reaction time and the reaction temperature is propitious to the formation of star anise-microstructured CuO.And star anise-microstructured CuO has a good optical absorption property.At last,the formation mechanism of star anise-microstructured CuO is discussed.%以1 mmol CuCl2为铜源和1mmol Na2CO3为辅助盐,利用简单的水热法在240℃和48h下合成了八角微米结构CuO.水热法合成试样的物相、形貌和光吸收特性分别被X射线衍射(XRD)、热场发射扫描电子显微镜(SEM)和紫外可见分光光度计(UV-VIS)表征.研究结果表明:水热法所合成试样的物相均为CuO.随着反应温度的增加和反应时间的延长,它们都有利于合成八角微米结构的CuO.并且此八角微米结构的CuO具有良好的光吸收能力.最后,对水热法合成八角微米结构CuO的机理进行了讨论.

  9. Structural refinement and photoluminescence properties of irregular cube-like (Ca{sub 1-x}Cu{sub x})TiO{sub 3} microcrystals synthesized by the microwave-hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, L.H., E-mail: larissahelena2009@gmail.com [DQ-UFSCar-Universidade Federal de Sao Carlos, P.O. Box 676, 13565-905 Sao Carlos, SP (Brazil); Moura, A.P. de; Mazzo, T.M. [UNESP-Universidade Estadual Paulista, P.O. Box 355, 14801-907 Araraquara, SP (Brazil); Ramirez, M.A. [UNESP-Universidade Estadual Paulista, 12516-410 Guaratingueta, SP (Brazil); Cavalcante, L.S.; Antonio, S.G.; Avansi, W. [UNESP-Universidade Estadual Paulista, P.O. Box 355, 14801-907 Araraquara, SP (Brazil); Mastelaro, V.R. [IFSC-USP, AV. Trabalhador Sao Carlense 400, 13560-970 Sao Carlos, SP (Brazil); Longo, E. [DQ-UFSCar-Universidade Federal de Sao Carlos, P.O. Box 676, 13565-905 Sao Carlos, SP (Brazil); UNESP-Universidade Estadual Paulista, P.O. Box 355, 14801-907 Araraquara, SP (Brazil); Varela, J.A. [UNESP-Universidade Estadual Paulista, P.O. Box 355, 14801-907 Araraquara, SP (Brazil)

    2012-09-14

    In this paper, calcium copper titanate (Ca{sub 1-x}Cu{sub x})TiO{sub 3} microcrystals with (x = 0, 0.01 and 0.02) were synthesized by the microwave-hydrothermal method at 140 Degree-Sign C for 30 min. These crystals were analyzed by X-ray diffraction (XRD), Rietveld refinement, X-ray absorption near-edge structure spectroscopy (XANES), micro-Raman spectroscopy, field emission scanning electron microscopy (FE-SEM). Its optical properties were investigated by ultraviolet-visible (UV-vis) absorption and photoluminescence (PL) measurements. XRD patterns, Rietveld refinement and micro-Raman spectroscopy indicated that these crystals present a perovskite-type orthorhombic structure. The Rietveld refinement data, micro-Raman and XANES spectra suggested that the substitution of Ca by Cu in A-site promoted a displacement of Ti atoms to off-center symmetric, which leads distortions on the cuboctahedral [CaO{sub 12}] clusters neighboring and consequently promotes a strain into the CaTiO{sub 3} lattice. FE-SEM images showed that these cube-like microcrystals have an irregular shape due to Ostwald-ripening and self-assembly of plates and cubes in growth process. The defects and distortions into lattice at medium- and short-range on the [CaO{sub 12}]/[TiO{sub 6}] clusters promotes the structural order-disorder responsible by the intense PL properties of these microcrystals. The microcrystals are promising candidates for future applications in optical devices. Highlights: Black-Right-Pointing-Pointer Any secondary phases were detected in the (Ca{sub 1-x}Cu{sub x})TiO{sub 3} powders. Black-Right-Pointing-Pointer Cu atoms are able to induce a local polarization in [CaO{sub 12}] and [TiO{sub 6}] clusters. Black-Right-Pointing-Pointer Ostwald-ripening and self-assembly are dominant mechanisms of these microcrystals. Black-Right-Pointing-Pointer PL emission presents a shift to green region as the concentration of Cu increases.

  10. Parametric studies on iron-carbon composite nanoparticles synthesized by laser pyrolysis for increased passivation and high iron content

    Science.gov (United States)

    Dumitrache, F.; Morjan, I.; Fleaca, C.; Birjega, R.; Vasile, E.; Kuncser, V.; Alexandrescu, R.

    2011-04-01

    Iron/iron carbide core and carbon shell nanoparticles with improved magnetic properties were successfully synthesized by laser pyrolysis. As iron and carbon precursors, iron pentacarbonyl and pure or argon-diluted acetylene/ethylene mixtures, respectively, were used. The aim of the present optimization is the improvement of the magnetic properties of the nanomaterials by the increase of the iron percent in powders simultaneously to the maintaining of the protective character of the carbon coverage of nanoparticles. The chemical content and the crystalline structure were monitored by EDX, XRD and TEM techniques. In the first study, the content of acetylene as carbon source was diminished from 75% to 0%. Consequently the percent iron increased from 10 at.% to 28 at.% while oxygen remained relatively constant (around 5 at.%). In the second step, only diluted ethylene was used (maximum 87.5 vol.% Ar). In this case, an increase of iron to 46 at.% is observed. An optimum 50% carbon source dilution was found. Above this value, the carbon content increases and below it, superficial oxidation increases through the diminishing of the carbon shell. The magnetic properties and the Fe phase composition of the Fe-C samples were analyzed by temperature dependent Mössbauer spectroscopy.

  11. Magnetic properties of ferrite-titanate nanostructured composites synthesized by the polyol method and consolidated by spark plasma sintering

    Science.gov (United States)

    Acevedo, Ulises; Gaudisson, Thomas; Ortega-Zempoalteca, Raul; Nowak, Sophie; Ammar, Souad; Valenzuela, Raul

    2013-05-01

    Multiferroic systems formed by a mixing of a ferroelectric phase and a ferrimagnetic phase are receiving significant attention because of their wide possibilities for tailoring properties. In this work, the magnetic properties of the cobalt ferrite-barium titanate system were investigated on samples prepared by an original combination of synthesis methods. Cobalt ferrite and barium titanate nanoparticles were synthesized separately by hydrolysis of the metal acetates in a polyol method. Both materials were mixed in a 1:1 ratio and consolidated by spark plasma sintering at 500 °C for 5 min. A high density nanostructured ceramic was obtained with grains smaller than 100 nm and a density about 80% of the theoretical value. Magnetic hysteresis loops showed a hard magnet behavior, with a coercive field larger than cobalt ferrite alone prepared under the same conditions. δM reversible magnetization plots exhibited dipolar interactions with a maximum at the coercive field. These results are interpreted in terms of an efficient mixing of the components, which strongly decreases the magnetic percolation in the composite by separating ferrite grains by titanate grains.

  12. Effect of biomass pretreatment on the product distribution and composition resulting from the hydrothermal liquefaction of short rotation coppice willow

    DEFF Research Database (Denmark)

    Grigoras, Ionela; Stroe, Rodica-Elisabeta; Sintamarean, Iulia-Maria

    2017-01-01

    from the HTL of willow and proposes short rotation coppice as an alternative biomass feedstock for biofuels production. Alkaline–thermal pretreatment, besides making high dry matter pumpable feedstock slurries, also led to an increase in the production of the bio-crude product with an oxygen content......A major challenge for the implementation of hydrothermal liquefaction (HTL) as a continuous process is the formulation of lignocellulosic feedstock, which is prone to phase separation into water and biomass parts when pressurized. One approach to remedy such phase separation is to reduce the dry...

  13. Nitrogen Dioxide-Sensing Properties at Room Temperature of Metal Oxide-Modified Graphene Composite via One-Step Hydrothermal Method

    Science.gov (United States)

    Zhang, Dongzhi; Liu, Jingjing; Xia, Bokai

    2016-08-01

    A metal oxide/graphene composite film-based sensor toward room-temperature detection of ppm-level nitrogen dioxide (NO2) gas has been demonstrated. The sensor prototype was constructed on a PCB substrate with microelectrodes, and a tin oxide-reduced graphene oxide (SnO2-rGO) composite as sensing film was prepared by one-step hydrothermal synthesis of tin tetrachloride pentahydrate solution in the presence of graphene oxide (GO). The SnO2-rGO hybrid composite was examined by scanning electron microscope and x-ray diffraction (XRD). The gas sensing properties of the SnO2-rGO composite were investigated at room temperature by exposing it to a wide concentration ranging from 1 ppm to 2000 ppm toward NO2 gas. The experiment results showed that the sensor exhibited a high response, superior selectivity, good repeatability, rapid response/recovery characteristics and low detection limit of 1 ppm, which exceeded that of a pure rGO sensor. The gas sensing mechanisms of the proposed sensor toward NO2 were possibly attributed to the nano-hybrid structures and n- p heterojunctions created at the interface of the SnO2 nanocrystals and rGO nanosheets.

  14. Hydrothermal synthesis of Li4-xNaxTi5O12 and Li4-xNaxTi5O12/graphene composites as anode materials for lithium-ion batteries

    Directory of Open Access Journals (Sweden)

    Zhu Jiping

    2016-01-01

    Full Text Available A potential Lithium-ion battery anode material Li4-xNaxTi5O12 (0≤x≤0.15 has been synthesized via a facile hydrothermal method with short processing time and low temperature. The XRD and FE-SEM results indicate that samples with Na-doped are well-crystallized and have more homogeneous particle distributions with smaller overall particle size in the range of 300-600nm. Electrochemical tests reveal that Na-doped samples exhibit impressive specific capacity and cycle stability compared to pristine Li4Ti5O12 at high rate. The Li3.9Na0.1Ti5O12 electrode deliver an initial specific discharge capacity of 169mAh/g at 0.5C and maintained at 150.4mAh/g even after 40 cycles with the reversible retention of 88.99%. Finally, a simple solvothermal reduction method was used to fabricate Li3.9Na0.1Ti5O12/graphene(Li3.9Na0.1Ti5O12/G composite. Galvanostatic charge-discharge tests demonstrate that this sample has remarkable capacities of 197.4mAh/g and 175.5mAh/g at 0.2C and 0.5C rate, respectively. This indicates that the Li3.9Na0.1Ti5O12/G composite is a promising anode material for using in lithium-ion batteries.

  15. Shallow vs. Deep Fluid Sources In Hydrothermal Systems: New Insights From VOC Composition In Fumarolic Discharges And Soil Gases Of Yellowstone National Park (USA)

    Science.gov (United States)

    Tassi, F.; Capecchiacci, F.; Montegrossi, G.; Caliro, S.; Chiodini, G.; Vaselli, O.

    2008-12-01

    The origin of non-methane volatile organic compounds (VOCs) in hydrothermal fluids is related to two distinct mechanisms regulated by different thermodynamic conditions (e.g. Des Marais et al., 1981; Mango, 2000; Capaccioni and Mangani, 2001): i) thermogenic reactions, such as catalytic reforming and/or thermal cracking, which proceed within the main reservoir at medium-to-high temperature (150-350°C) and reduced conditions; ii) biodegradation processes, occurring at relatively shallow depth, where uprising fluids have oxidizing conditions. According to these considerations, the main aim of the present investigation is to discriminate the different fluid sources feeding the hydrothermal system on the basis of the C2-C15 organic compounds in fumarolic discharges and soil gases collected at the Yellowstone National Park (USA). A total of 64 and 66 different species were identified in the gas discharges and in the soil gas samples, respectively. The composition of the organic gas fraction in the fumarolic fluids is relatively homogeneous, being dominated by C2-C6 alkanes (81 %) and showing relatively high concentrations of alkenes (13 %), aromatics (3.7 %) and cyclics (1.4 %). Differently, the relative percentages of alkanes and alkenes in the soil gas, where VOC abundances are about two orders of magnitude less abundant than those in the gas discharges, are significantly lower (64 and 6.8 %, respectively) and cyclics are absent. On the other hand, oxygenated species (17.8 %), aromatics (5.6 %) and Cl-bearing compounds (4.5 %) results to be enriched with respect to those measured in the gas vents. Such compositional differences are likely to be due to the bacterial activity in the soil that causes the production of ketones, esters, alcohols, aldehydes and organic acids from the C-H species (hydrocarbons sensu strictu). Organic acids, mainly constituted by ossalic acid and traces of tartaric, malonic citric and succinic ones, were also determined in the fumarolic

  16. Role of chemical composition of oxide layer on stainless steel for ZrO{sub 2} coating by hydrothermal process

    Energy Technology Data Exchange (ETDEWEB)

    Garg, Nidhi; Mittal, Vinit K; Bera, Santanu; Chandramohan, P. [Water and Steam Chemistry Division, BARC Facilities, Kalpakkam (India); Das, C.R. [Materials Technology Division, IGCAR, Kalpakkam (India); Velmurugan, S., E-mail: svelu@igcar.gov.in [Water and Steam Chemistry Division, BARC Facilities, Kalpakkam (India)

    2013-10-31

    Thin films of ZrO{sub 2} have been developed by hydrothermal process on pre-oxidized stainless steel (SS) surfaces composed of different oxides like spinels or α-Fe{sub 2}O{sub 3}. Variations in thicknesses and uniformity of ZrO{sub 2} films have been observed on different pre-oxidized SS surfaces. Raman scattering spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy and X-ray diffraction techniques have been used to explain mechanisms of formation of ZrO{sub 2} films on various pre-oxidized SS surfaces. A pre-oxidized layer of α-Fe{sub 2}O{sub 3} seems to be an ideal oxide on the SS surface for uniform coating of ZrO{sub 2}. This may be attributed to close match of lattice parameters of ZrO{sub 2} with that of α-Fe{sub 2}O{sub 3}. - Highlights: • Developed tetragonal ZrO{sub 2} films on stainless steel (SS) by hydrothermal process. • α-Fe{sub 2}O{sub 3} on SS is prerequisite for uniformly thick and crystalline ZrO{sub 2} coatings. • Spinels and α-Fe{sub 2−x}Cr{sub x}O{sub 3} on SS result in thin and non-uniform ZrO{sub 2} coating.

  17. A Novel Strategy for Preparation of Si-HA Coatings on C/C Composites by Chemical Liquid Vaporization Deposition/Hydrothermal Treatments.

    Science.gov (United States)

    Xin-Bo, Xiong; Xin-Ye, Ni; Ya-Yun, Li; Cen-Cen, Chu; Ji-Zhao, Zou; Xie-Rong, Zeng

    2016-08-05

    A novel strategy for the preparation of Si-doped hydroxyapatite (Si-HA) coatings on H2O2-treated carbon/carbon composites (C/C) was developed. HA coating was prepared on C/C through chemical liquid vaporization deposition (CLVD)/hydrothermal treatment. HA coating was immersed in an H2SiO3 solution at an autoclave at 413 K for transformation into Si-HA coating. The effects of H2SiO3 mass contents on the phase, morphology, and composition of the Si-HA coatings were studied through SEM, EDS,XRD, and FTIR. Their bonding performance to C/C was measured through a scratch test. Under the optimal content condition, the in vitro skull osteoblast response behaviors of the Si-HA coating were evaluated. Results showed that SiO3(2-) could enter into the HA lattice and occupy the PO4(3-) sites. Doped SiO3(2-) significantly improved the bonding performance of the HA coating to C/C in comparison with the untreated HA. The adhesive strength of the coatings initially increased and then decreased with increasing H2SiO3 content. Meanwhile, the cohesive strength of the Si-HA coatings was almost nearly identical. The Si-HA coating achieved at a content of 90% H2SiO3 exhibited the best bonding performance, and its osteoblast compatibility in vitro was superior to that of the untreated HA coating on C/C through CLVD/hydrothermal treatment.

  18. A Novel Strategy for Preparation of Si-HA Coatings on C/C Composites by Chemical Liquid Vaporization Deposition/Hydrothermal Treatments

    Science.gov (United States)

    Xin-Bo, Xiong; Xin-Ye, Ni; Ya-Yun, Li; Cen-Cen, Chu; Ji-Zhao, Zou; Xie-Rong, Zeng

    2016-08-01

    A novel strategy for the preparation of Si-doped hydroxyapatite (Si-HA) coatings on H2O2-treated carbon/carbon composites (C/C) was developed. HA coating was prepared on C/C through chemical liquid vaporization deposition (CLVD)/hydrothermal treatment. HA coating was immersed in an H2SiO3 solution at an autoclave at 413 K for transformation into Si-HA coating. The effects of H2SiO3 mass contents on the phase, morphology, and composition of the Si-HA coatings were studied through SEM, EDS,XRD, and FTIR. Their bonding performance to C/C was measured through a scratch test. Under the optimal content condition, the in vitro skull osteoblast response behaviors of the Si-HA coating were evaluated. Results showed that SiO32‑ could enter into the HA lattice and occupy the PO43‑ sites. Doped SiO32‑ significantly improved the bonding performance of the HA coating to C/C in comparison with the untreated HA. The adhesive strength of the coatings initially increased and then decreased with increasing H2SiO3 content. Meanwhile, the cohesive strength of the Si-HA coatings was almost nearly identical. The Si-HA coating achieved at a content of 90% H2SiO3 exhibited the best bonding performance, and its osteoblast compatibility in vitro was superior to that of the untreated HA coating on C/C through CLVD/hydrothermal treatment.

  19. Synergetic adsorption and photocatalytic degradation of pollutants over 3D TiO2-graphene aerogel composites synthesized via a facile one-pot route.

    Science.gov (United States)

    Zhang, Jing-Jie; Wu, Yu-Hui; Mei, Jin-Ya; Zheng, Guang-Ping; Yan, Ting-Ting; Zheng, Xiu-Cheng; Liu, Pu; Guan, Xin-Xin

    2016-08-01

    A series of composites consisting of anatase TiO2 nanocrystals and three-dimensional (3D) graphene aerogel (TiO2-GA) were self-assembled directly from tetrabutyl titanate and graphene oxides via a one-pot hydrothermal process. TiO2 was found to uniformly distribute inside the 3D network of GA in the resulting composites with large surface areas (SBET > 125 m(2) g(-1)) and high pore volumes (Vp > 0.22 cm(3) g(-1)). In comparison with GA and TiO2, the composites possessed much higher adsorption capacities and visible light photocatalytic activity in the degradation of rhodamine B (RhB). With an initial concentration of 20.0 mg L(-1) of RhB, the adsorptive decolourization of RhB was as high as 95.1% and the total decolourization value reached up to 98.7% under visible light irradiation over 5.0 mg of the resulting composites. It was elucidated that the physical and chemical properties of the TiO2-GA composites could be ascribed to their unique 3D nanoporous structure with high surface areas and the synergetic activities of graphene nanosheets and TiO2 nanoparticles.

  20. Surfactant Assisted Hydrothermal Synthesis of CdSe Nanostructural Materials

    Institute of Scientific and Technical Information of China (English)

    Ganganagappa Nagaraju; Cujjarahalli Thimmanna Chandrappa

    2012-01-01

    CdSe/CTAB composite nanostructural materials were successfully synthesized at 160-200℃ for 2 days through a facile surfactant (cetyl trimethyl ammonium bromide-CTAB) assisted hydrothermal method us- ing cadmium acetate and sodium selenate as precursor. The obtained products were characterized by X-ray diffraction, energy dispersive X-ray analysis, Fourier transform infrared spectroscopy and thermo gravimetric analysis. Optical properties were studied by photoluminescence and UV-visible spectroscopy and morphology was investigated by scanning electron microscopy.

  1. 水热合成纳米NiFe2O4的光催化性能%Photocatalytic Properties of Nano-NiFe204 Synthesized by Hydrothermal Method

    Institute of Scientific and Technical Information of China (English)

    赵晓华; 娄向东; 李新莉

    2011-01-01

    利用水热法在160℃下反应8 h后合成纳米NiFe2O4粉体.利用X射线衍射(XRD)、透射电镜(TEM)等对样品进行表征,测试了样品对B-GFF黑、K-GL翠蓝、B-RN蓝等活性染料的光催化性能,研究了光源、初始染料浓度、光照时间及催化剂的回收等对染料降解率的影响.结果表明,制备的NiFe2O4粉体为圆形晶粒,平均粒径在15 am左右.无光照条件下,NiFeO4对三种活性染料有一定的催化降解.氙灯照射6 h后,NiFe2O4对B-GFF黑、B-RN蓝及K-GL翠蓝分别可达到93%、85%及58%以上的降解.紫外灯照射效果最好,紫外光照2 h后,该催化剂对B-GFF黑及B-RN蓝基本可达到100%的降解,对K-GL翠蓝也可达到75%的降解.回收后的NiFe2O4催化剂对B-GFF黑溶液仍具有75%的降解率.%Nano-NiFe2O4 was prepared by hydrothermal method synthesized at 160 ℃ for 8 h. The sample was characterized by X-ray diffraction and transmission electron microscopy. The sample photocatalytic activity was studied by probing the degradation date of reactive dyes including Black B-GFF, Turquoise Blue K-GL and Blue B-RN. The effects of light source, initial dyes concentrations, illumination time and reclaimed catalyst on degradation rate of dyes were also investigated. The results show that the NiFe204 powem as-prepared were circled shape and the average grain size of the powders was about 15 nm. All the dyes could be partly degraded by NiFe2O4 without illumination. After irradiation 6 h with xenon lamp, the Black B-GFF, Blue B-RN and Turquoise Blue K-GL could be degraded to above 93%, 85% and 58%, respectively. While under the UV light irradiation, the NiFe2O4 catalyst have the highest photodegradation activity, the degradation rates of Black B-GFF and Blue B-RN may achieve nearly 100% after 2 h illumination, also, the degradation rate of Turquoise Blue K-GL could reach 75%. In addition, with reclaimed NiFe2O4 catalyst, the degradation rate of Black B-GFF was 75%.

  2. A Comparative Study of the Adsorption of Methylene Blue onto Synthesized Nanoscale Zero-Valent Iron-Bamboo and Manganese-Bamboo Composites

    Directory of Open Access Journals (Sweden)

    Solomon E. Shaibu

    2014-06-01

    Full Text Available In this study, bamboo impregnated with nanoscale zero-valent iron (nZVI and nanoscale manganese (nMn were prepared by the aqueous phase borohydride reduction method and characterized using scanning electron microscopy (SEM, Fourier transform infrared spectroscopy (FTIR and PIXE analysis. The synthesized nMn-bamboo and nZVI-bamboo composites were subsequently applied to the sorption of methylene blue (MB dye from aqueous solution. The adsorption of MB dye was investigated under various experimental conditions such as pH, contact time, initial concentration of MB dye and adsorbent dosage. The results showed that the synthesized nZVI-bamboo composite was more effective than nMn-bamboo composite in terms of higher MB dye adsorption capacity of 322.5 mg/g compared to 263.5 mg/g of nMn-bamboo composite. At a concentration of 140 mg/L MB dye, 0.02 g of nZVI-bamboo and nMn-bamboo composites resulted in 79.6% and 78.3% removal, respectively, at 165 rpm, contact time of 120 min and at a solution pH of 7.6. The equilibrium data was best represented by Freundlich isotherm model and the pseudo-second order kinetic model better explained the kinetic data for both nZVI-bamboo and nMn-bamboo composites.

  3. Hydrothermal Fabrication of Silver Nanowires-Silver Nanoparticles-Graphene Nanosheets Composites in Enhancing Electrical Conductive Performance of Electrically Conductive Adhesives

    Directory of Open Access Journals (Sweden)

    Hongru Ma

    2016-06-01

    Full Text Available Silver nanowires-silver nanoparticles-graphene nanosheets (AgNWs-AgNPs-GN hybrid nanomaterials were fabricated through a hydrothermal method by using glucose as a green reducing agent. The charge carriers of AgNWs-AgNPs-GN passed through defect regions in the GNs rapidly with the aid of the AgNW and AgNP building blocks, leading to high electrical conductivity of electrically conductive adhesives (ECA filled with AgNWs-AgNPs-GN. The morphologies of synthesized AgNWs-AgNPs-GN hybrid nanomaterials were characterized by field emission scanning electron microscope (FESEM, and high resolution transmission electron microscopy (HRTEM. X-ray diffraction (XRD and laser confocal micro-Raman spectroscopy were used to investigate the structure of AgNWs-AgNPs-GN. The resistance of cured ECAs was investigated by the four-probe method. The results indicated AgNWs-AgNPs-GN hybrid nanomaterials exhibited excellent electrical properties for decreasing the resistivity of electrically conductive adhesives (ECA. The resistivity of ECA was 3.01 × 10−4 Ω·cm when the content of the AgNWs-AgNPs-GN hybrid nanomaterial was 0.8 wt %.

  4. Synthesis of LiFePO4/Li2SiO3/reduced Graphene Oxide (rGO) Composite via Hydrothermal Method

    Science.gov (United States)

    Arifin, M.; Iskandar, F.; Aimon, A. H.; Munir, M. M.; Nuryadin, B. W.

    2016-08-01

    LiFePO4 is a type of cathode active material used for lithium ion batteries. It has a high electrochemical performance. However, it suffers from certain disadvantages such as a very low intrinsic electronic conductivity and low ionic diffusion. This study was conducted to increase the conductivity of LiFePO4. We have investigated the addition of Li2SiO3 and reduced graphene oxide (rGO) to LiFePO4. The objective of this research was to synthesize LiFePO4/Li2SiO3/rGO via hydrothermal method. Fourier transform infrared spectroscopy (FTIR) measurement showed that the peaks corresponded to the vibration of LiFePO4/Li2SiO3. Further, X-ray diffraction (XRD) measurement confirmed a single phase of LiFePO4. Finally, scanning electron microscopy (SEM) images showed that rGO was distributed on the LiFePO4/Li2SiO3 structure.

  5. Silver Doped TiO2 Nanostructure Composite Photocatalyst Film Synthesized by Sol-Gel Spin and Dip Coating Technique on Glass

    OpenAIRE

    Mojtaba Nasr-Esfahani; Mohammad Hossein Habibi

    2008-01-01

    New composite films (P25SGF-MC-Ag, MPC500SGF-MC-Ag, and ANPSGF-MC-Ag) have been synthesized by a modified sol-gel method using different particle sizes of TiO2 powder and silver addition. Nanostructure TiO2/Ag composite thin films were prepared by a sol-gel spin and dip coating technique. while, by introducing methyl cellulose (MC) porous, TiO2/Ag films were obtained after calcining at a temperature of 500°C. The as-prepared TiO2 and TiO2/Ag films were characterized by X-ray diffractometry, a...

  6. In situ hydrothermal syntheses, structures and photoluminescent properties of four novel metal-organic frameworks constructed by lanthanide (Ln=Ce(III), Pr(III), Eu(III)) and Cu(I) metals with flexible dicarboxylate acids and piperazine-based ligands

    Energy Technology Data Exchange (ETDEWEB)

    Ay, Burak; Karaca, Serkan [Department of Chemistry, Arts and Science Faculty, Çukurova University, 01330 Adana (Turkey); Yildiz, Emel, E-mail: eeyildiz@cu.edu.tr [Department of Chemistry, Arts and Science Faculty, Çukurova University, 01330 Adana (Turkey); Lopez, Valerie [Department of Chemistry, Syracuse University, Syracuse, NY 13244 (United States); Nanao, Max H. [European Molecular Biology Laboratory, Grenoble Outstation, 71 Avenue des Martyrs, CS 90181, 38042 Grenoble Cedex 9 (France); University Grenoble Alpes-Centre National de la Recherche Scientifique-EMBL Unit of Virus Host-Cell Interactions, 71 Avenue des Martyrs, CS 90181, 38042 Grenoble Cedex 9 (France); Zubieta, Jon [Department of Chemistry, Syracuse University, Syracuse, NY 13244 (United States); Université Grenoble Alpes Laboratoire de Physiologie Cellulaire & Végétale, Institut de Recherches en Technologies et Sciences pour le Vivant, 17 rue des Martyrs, 38054 Grenoble cedex 9 (France)

    2016-01-15

    Four novel metal-organic frameworks,[Cu{sub 2}Cl{sub 2}(pyrz)]{sub n} (1) and (H{sub 2}pip){sub n}[Ln{sub 2}(pydc){sub 4}(H{sub 2}O){sub 2}]{sub n} (Ln=Ce (2), Pr (3) and Eu (4), H{sub 2}pzdc=2,3-pyrazinedicarboxylic acid, pyrz=pyrazine, H{sub 2}pydc=2,6-pyridinedicarboxylic acid, H{sub 2}pip=piperazine) have been synthesized under hydrothermal conditions and characterized by the elemental analysis, ICP, Far IR (FIR), FT-IR spectra, TGA, single crystal X-ray diffraction analysis and powder X-ray diffraction (PXRD). Compound 1 is two-dimensional containing Cl-Cu-Cl sites, while the lanthanide complexes contain one-dimensional infinite Ln–O-Ln chains. All the complexes show high thermal stability. The complexes 1–3 exhibit luminescence emission bands at 584, 598 and 614 nm at room temperature when excited at 300 nm. Complex 4 exhibits bright red solid-state phosphorescence upon exposure to UV radiation at room temperature. - Graphical abstract: Four novel metal-organic frameworks have been synthesized under hydrothermal conditions. Thermal and luminescent properties of the compounds have been investigated.

  7. 水热法制备的LuFeO3晶粒的超声催化活性%Sonocatalytic activity of LuFeO3 crystallites synthesized via a hydrothermal route

    Institute of Scientific and Technical Information of China (English)

    周明; 杨华; 县涛; 杨阳; 张云川

    2015-01-01

    LuFeO3 crystallites of different sizes and morphologies were synthesized via a hydrothermal route. The sonocatalytic properties of the as‐synthesized samples were investigated by degrading various organic dyes, including acid orange 7 (AO7), rhodamine B (RhB), methyl orange (MO), and meth‐ylene blue (MB), under ultrasonic irradiation, revealing that they exhibit excellent sonocatalytic activity toward the degradation of these dyes. Particularly, the synthesized bar‐like particles with lengths of~3μm and widths of~1μm have the highest sonocatalytic activity, and the degradation percentage of AO7 reaches 89%after 30 min of sonocatalysis. The effects of inorganic anions such as Cl−, NO3−, SO42−, PO43−, and HCO3− on the sonocatalysis efficiency were investigated. Hydroxyl radicals (•OH) detected by fluorimetry using terephthalic acid as a probe molecule were found to be produced over the ultrasonic‐irradiated LuFeO3 particles. The addition of ethanol, which acts as a•OH scavenger, leads to quenching of •OH radicals and a simultaneous decrease in the dye degrada‐tion. This suggests that•OH is the dominant active species responsible for the dye degradation.%超声波在水中传播时会产生大量空化气泡,空化气泡经历成核、生长和瞬间崩塌等过程,并在崩塌瞬间产生局部高温和高压,过程中会发出瞬间闪光,即声致发光.局部高温高压及声致发光可将半导体价带上的电子激发至导带,形成电子/空穴对,电子和空穴迁移至半导体颗粒表面,参与一系列氧化还原反应致使有机污染物发生分解.由于超声波在各种液体中都具有很强的穿透能力,因此与半导体光催化技术相比,半导体超声催化技术在降解高浓度和不透明染料废水时具有明显优势. LuFeO3是稀土正铁氧体中的一员,具有独特磁结构、巨介电常数及多铁性,近年来引起了人们极大的研究兴趣.同时, LuFeO3也是一种窄带隙半

  8. Microwave Dielectric Properties of LaPO4 Ceramics Synthesized by a Hydrothermal Method%水热法合成陶瓷LaPO4的微波介电性能

    Institute of Scientific and Technical Information of China (English)

    谢会东; 李飞; 陈超; 席海红; 史玲

    2015-01-01

    Lanthanum orthophosphate (LaPO4) ceramics were obtained by using hydrothermal prepared powders and solid-state reaction prepared powders in a sintering temperature range of 1030–1340℃ and 1300–1460℃, respectively. The sintering and microwave dielectric properties of hydrothermal processed LaPO4 ceramics were compared with those of solid-state reaction processed LaPO4. The results showed that hydrothermal processed LaPO4 had a higher sinterability and better microwave dielectric properties due to its much finer particle size when compared with solid-state reaction processed LaPO4. The best microwave dielectric properties of the hydrothermal processed LaPO4 ceramics were obtained when the ceramics sintered at 1260℃ for 2 h with a permittivity~10.2, aQ×f value about 129704 GHz (at 10.2 GHz) and a temperature coefficient value of –58.6×10-6/℃. TheQ×f value of hydrothermal processed LaPO4 ceramics was 2.47 times greater than that of solid-state reaction processed LaPO4 ceramics, while the sintering temperature of the former was 140℃ lower than that of the latter in the literature.%通过水热法和固相反应法制备了 LaPO4粉体,分别在1030~1340℃和1300~1460℃范围内对粉体进行了烧结,得到了LaPO4陶瓷,研究对比了两种方法得到的陶瓷的烧结行为和微波介电性能。结果表明:和固相法相比,水热法得到的陶瓷由于粉体粒径小更易于烧结,微波介电性能更优;在1260℃条件下烧结2 h得到的水热法陶瓷具有最好的微波介电性能:介电常数为10.2, Q×f值为129704 GHz (f=10.2 GHz),谐振频率温度系数值为–58.6 ppm/℃;水热法陶瓷的Q×f值为固相法的2.47倍,烧结温度比固相法低140℃。

  9. Hydrothermal Preparation and Characterization of TiO2 /BiVO4 Composite Catalyst and its Photolysis of Water to Produce Hydrogen.

    Science.gov (United States)

    Jian, Zicong; Huang, Shaobin; Cao, Yaya; Zhang, Yongqing

    2016-05-01

    In the present work, bismuth vanadate composited photocatalysts were synthesized and characterized. X-ray diffractometry and Raman results showed that the particles were well crystallized, and formed by the complex of monoclinic BiVO4 and TiO2 . On electron microscopy, the photocatalyst exhibited high crystallization, agglutination and irregular shape, and was surrounded by numerous TiO2 particles. The study of surface areas showed that the specific surface area of 30-BiVO4 /TiO2 composited was 112 m(2) ·g(-1) , which was nearly 10 times that of pure BiVO4 . The ultraviolet-visible diffuse reflectance spectra indicated the composited photocatalyst were activated in visible light. The activity of photocatalytic water splitting was studied. The results showed that monomer BiVO4 photocatalyst was not able to produce hydrogen under any light source. BiVO4 /TiO2 composited photocatalysts, however, were capable of generating hydrogen. Under UV light irradiation for 120 min, 1 g catalyst dispersed in 50 mL deionized water produced almost 1 mL hydrogen, such that the productivity of hydrogen was higher than that of P25-TiO2 . Photocatalytic decomposition of water under visible light also confirmed that the BiVO4 /TiO2 composited photocatalyst had the ability of water splitting.

  10. Excellent electromagnetic absorption properties of poly(3,4-ethylenedioxythiophene)-reduced graphene oxide-Co3O4 composites prepared by a hydrothermal method.

    Science.gov (United States)

    Liu, Pan-Bo; Huang, Ying; Sun, Xu

    2013-12-11

    The ternary composites of poly(3,4-ethylenedioxythiophene)-reduced graphene oxide-Co3O4 (PEDOT-RGO-Co3O4) were synthesized and the electromagnetic absorption property of the composites was investigated. The structure of the composites was characterized with Fourier-transform infrared spectra, X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, and transmission electron microscope. The electromagnetic parameters indicate the enhanced electromagnetic absorption property of the composites was attributed to the better impedance matching. On the basis of the above characterization, an electromagnetic complementary theory was proposed to explain the impedance matching. It can be found that the maximum reflection loss of PEDOT-RGO-Co3O4 can reach -51.1 dB at 10.7 GHz, and the bandwidth exceeding -10 dB is 3.1 GHz with absorber thickness of 2.0 mm. Therefore, the PEDOT-RGO-Co3O4 composites, with such excellent electromagnetic absorption properties and wide absorption bandwidth, can be used as a new kind of candidate for microwave absorbing materials.

  11. Preparation and Photocatalytic of Nanoneedle Bi/ZnWO₄by Two-Step Hydrothermal Method.

    Science.gov (United States)

    Chen, Haifeng; Guo, Lingmei; Zhang, Dandan; Li, Jingxin; Liu, Shipin; Li, Bin

    2016-01-01

    Nanoneedle Bi/ZnWO₄ photocatalysts were successfully synthesized using a two-step hydrothermal method. In the first hydrothermal experiment ZnO/ZnWO₄ nanoneedle crystals were synthesized from NaWO₄· 2H₂O and Zn(NO₃)₂· 6H₂O, using polyacrylamide (PAM) as a template in a hydrothermal environment. Bi cations were then reduced by t-BuONa in a second hydrothermal experiment, adding nanoneedle ZnO/ZnWO₄. The catalysts were then characterized by powder X-ray diffraction (XRD), scanning electron microcopy (SEM), energy dispersive spectrometer (EDS) and UV-vis diffuse reflectance spectrum (DRS). The results show that by adding Bi nanoparticles, the composition of the mixture gradually changed from that of ZnO/ZnWO₄ to Bi/ZnWO₄. The nanoneedle Bi/ZnWO₄samples displayed better UV light photocatalysis than the nanoneedle ZnO/ZnWO₄ samples. The optimum concentration of Bi was investigated using a photocatalytic experiment. A "blue shift" was observed when the molar ratio of Bi was increased.

  12. Microstructure of in-situ Synthesized (TiB+TiC)/Ti Composites Prepared by Hot-pressing

    Institute of Scientific and Technical Information of China (English)

    Zhenzhu ZHENG; Lin GENG; Honglin WANG; Weimin ZHOU; Hongyu XU

    2003-01-01

    In-situ 5 vol.pct TiB whiskers and TiC particulates reinforced Ti composites were fabricated by blending Ti powderand B4C particulates followed by reactive hot-pressing. The microstructure of the composites was investigated byusing differential scanning c

  13. Electromagnetic absorption properties of flowerlike cobalt composites at microwave frequencies

    Institute of Scientific and Technical Information of China (English)

    Liu Tao; Zhou Pei-Heng; Liang Di-Fei; Deng Long-Jiang

    2012-01-01

    In this work,we report the electromagnetic absorption(EMA)properties of composites consisting of micrometersized cobalt with flowerlike architecture synthesized by a facile hydrothermal reduction method.Compared with the conventional spherical Co-paraffin composites,the flowerlike Co-paraffin composites are favorable with respect to EMA performance in the low frequency region,ascribing interfacial polarization loss and Ohmic loss to the improvement in the impedance match.

  14. Hydrothermal syntheses and single crystal structural characterization of M(H2O)6(OPTA)2 [M = Co(II), Ni(II), Zn(II); OPTA = 1-oxopyridinium-2-thioacetato

    Indian Academy of Sciences (India)

    S Kumaresan; P Ramadevi; R D Walsh; A McAneny; C H Lake

    2006-05-01

    A new class of compounds of the family M(H2O)6(OPTA)2 (where M = Co(II), Ni(II), and Zn(II); OPTA = 1-oxopyridinium-2-thioacetato) was prepared from the appropriate metal acetates, 1-oxopyridinium-2-thioacetic acid (OPTAH), and potassium hydroxide in hydrothermal media and structurally characterized. The structure is constructed from M(H2O)$_{6}^{2+}$ and two anions of OPTAH (C7H6NO3S) linked through hydrogen bonding into an extended network.

  15. Effects of in situ synthesized mullite whisker on mechanical properties of Al2O3-SiC composite by microwave sintering

    Science.gov (United States)

    Dang, Xudan; Wei, Meng; Fan, Bingbing; Guan, Keke; Zhang, Rui; Long, Weimin; Zhang, Hongsong

    2017-06-01

    In situ synthesis of mullite whisker was introduced to Al2O3-SiC composite by microwave sintering. The effects of sintering parameters (sintering temperature, holding time and SiC particle size) on thermal shock resistance of Al2O3-SiC composite were also studied in this paper. Original SiC particles coated with SiO2 by a sol-gel method were reacted with Al2O3 particles, resulting in the in situ growth of mullite. The phase composition was identified by x-ray diffraction (XRD). The bridging of mullite whisker between Al2O3 and SiC particles was observed by scanning electron microscopy (SEM) analysis. The thermal shock resistance of samples was investigated through the combination of water quenching and three-point bending methods. The results show that the thermal shock resistance of Al2O3-SiC composite with mullite whisker reinforced remarkably, indicating better mechanical properties than the Al2O3-SiC composite without mullite whisker. Finally, the optimum process parameters (the sintering temperature of 1500 °C, the holding time of 30 min, and the SiC particle size of 5 µm) for toughening Al2O3-SiC composite by in situ synthesized mullite whisker were obtained.

  16. Microwave-synthesized freestanding iron-carbon nanotubes on polyester composites of woven Kevlar fibre and silver nanoparticle-decorated graphene.

    Science.gov (United States)

    Hazarika, Ankita; Deka, Biplab K; Kim, DoYoung; Kong, Kyungil; Park, Young-Bin; Park, Hyung Wook

    2017-01-11

    We synthesized Ag nanoparticle-decorated multilayered graphene nanosheets (Ag-graphene) from graphite nanoplatelets and silver nitrate through 90-100 s of microwave exposure, without the use of any mineral acids or harsh reducing agents. Fe nanoparticle-decorated carbon nanotubes (Fe-CNTs) were grown on polypyrrole (PPy) deposited on woven Kevlar fibre (WKF), using ferrocene as a catalyst, under microwave irradiation. Fe-CNTs grown on WKF and Ag-graphene dispersed in polyester resin (PES) were combined to fabricate Ag-graphene/Fe-CNT/PPy-coated WKF/PES composites by vacuum-assisted resin transfer moulding. The combined effect of Fe-CNTs and Ag-graphene in the resulting composites resulted in a remarkable enhancement of tensile properties (a 192.56% increase in strength and 100.64% increase in modulus) as well as impact resistance (a 116.33% increase). The electrical conductivity significantly increased for Ag-graphene/Fe-CNT/PPy-coated WKF/PES composites. The effectiveness of electromagnetic interference shielding, which relies strongly on the Ag-graphene content in the composites, was 25 times higher in Ag-graphene/Fe-CNT/PPy-coated WKF/PES than in neat WKF/PES composites. The current work offers a novel route for fabricating highly promising, cost effective WKF/PES composites through microwave-assisted synthesis of Fe-CNTs and Ag-graphene.

  17. Microwave-synthesized freestanding iron-carbon nanotubes on polyester composites of woven Kevlar fibre and silver nanoparticle-decorated graphene

    Science.gov (United States)

    Hazarika, Ankita; Deka, Biplab K.; Kim, Doyoung; Kong, Kyungil; Park, Young-Bin; Park, Hyung Wook

    2017-01-01

    We synthesized Ag nanoparticle-decorated multilayered graphene nanosheets (Ag-graphene) from graphite nanoplatelets and silver nitrate through 90–100 s of microwave exposure, without the use of any mineral acids or harsh reducing agents. Fe nanoparticle-decorated carbon nanotubes (Fe-CNTs) were grown on polypyrrole (PPy) deposited on woven Kevlar fibre (WKF), using ferrocene as a catalyst, under microwave irradiation. Fe-CNTs grown on WKF and Ag-graphene dispersed in polyester resin (PES) were combined to fabricate Ag-graphene/Fe-CNT/PPy-coated WKF/PES composites by vacuum-assisted resin transfer moulding. The combined effect of Fe-CNTs and Ag-graphene in the resulting composites resulted in a remarkable enhancement of tensile properties (a 192.56% increase in strength and 100.64% increase in modulus) as well as impact resistance (a 116.33% increase). The electrical conductivity significantly increased for Ag-graphene/Fe-CNT/PPy-coated WKF/PES composites. The effectiveness of electromagnetic interference shielding, which relies strongly on the Ag-graphene content in the composites, was 25 times higher in Ag-graphene/Fe-CNT/PPy-coated WKF/PES than in neat WKF/PES composites. The current work offers a novel route for fabricating highly promising, cost effective WKF/PES composites through microwave-assisted synthesis of Fe-CNTs and Ag-graphene.

  18. Microwave-synthesized freestanding iron-carbon nanotubes on polyester composites of woven Kevlar fibre and silver nanoparticle-decorated graphene

    Science.gov (United States)

    Hazarika, Ankita; Deka, Biplab K.; Kim, DoYoung; Kong, Kyungil; Park, Young-Bin; Park, Hyung Wook

    2017-01-01

    We synthesized Ag nanoparticle-decorated multilayered graphene nanosheets (Ag-graphene) from graphite nanoplatelets and silver nitrate through 90–100 s of microwave exposure, without the use of any mineral acids or harsh reducing agents. Fe nanoparticle-decorated carbon nanotubes (Fe-CNTs) were grown on polypyrrole (PPy) deposited on woven Kevlar fibre (WKF), using ferrocene as a catalyst, under microwave irradiation. Fe-CNTs grown on WKF and Ag-graphene dispersed in polyester resin (PES) were combined to fabricate Ag-graphene/Fe-CNT/PPy-coated WKF/PES composites by vacuum-assisted resin transfer moulding. The combined effect of Fe-CNTs and Ag-graphene in the resulting composites resulted in a remarkable enhancement of tensile properties (a 192.56% increase in strength and 100.64% increase in modulus) as well as impact resistance (a 116.33% increase). The electrical conductivity significantly increased for Ag-graphene/Fe-CNT/PPy-coated WKF/PES composites. The effectiveness of electromagnetic interference shielding, which relies strongly on the Ag-graphene content in the composites, was 25 times higher in Ag-graphene/Fe-CNT/PPy-coated WKF/PES than in neat WKF/PES composites. The current work offers a novel route for fabricating highly promising, cost effective WKF/PES composites through microwave-assisted synthesis of Fe-CNTs and Ag-graphene. PMID:28074877

  19. Ages and compositions of primary and secondary allanite from the Lala Fe-Cu deposit, SW China: implications for multiple episodes of hydrothermal events

    Science.gov (United States)

    Chen, Wei Terry; Zhou, Mei-Fu

    2014-08-01

    Numerous Fe-Cu deposits in southwestern China form the Kangdian Iron-Oxide Copper-Gold (IOCG) metallogenic Province. These deposits have a close association of Fe-oxides and Cu-sulfides formed at different stages, which are possibly related to multiple hydrothermal events. In this paper, U-Pb dating and chemical analyses on allanite from different stages of the Lala deposit were used to constrain timing and origin of such events. Allanite occurs as disseminated grains or patches in Fe-Cu ores and is closely associated with chalcopyrite, molybdenite, calcite and minor titanite, postdating magnetite and apatite. High-resolution backscattered electronic (BSE) imaging, electron microprobe compositions and X-ray scanning profiles demonstrate that REE-rich primary allanite was replaced by later, relatively porous and REE-poor secondary allanite. Such a replacement was promoted by interaction between primary allanite and fluid fluxes infiltrating the minerals, following an exchange scheme of REE3+ + Fe2+ → Ca2+ + Al3+. The secondary allanite has higher Fe3+/(Fe3++Fe2+) ratios and U contents, indicating involvement of relatively oxidized fluids during alteration. The alteration has also produced unidentified secondary REE minerals in fractures, indicating re-deposition of some of the removed REEs. The primary and secondary allanites are dated by in situ LA-ICP-MS technique and have U-Pb ages of 1,067 ± 41 Ma and 880-850 Ma, respectively. The ~1.07 Ga primary allanite was contemporaneous with the main Mo-Cu-LREE mineralization with a molybdenite Re-Os age of ~1.08 Ga. The 880-850 Ma secondary allanite is comparable with the Ar-Ar ages (890-830 Ma) of biotite from hosting schists and undeformed sulfide veins occurring throughout the Kangdian Province, suggesting that such an event was possibly syn-deformational and represents a younger hydrothermal event. Occurrences of both primary and secondary allanites suggest that the mineralization may have involved multiple

  20. Effect of Fe(II)/Ce(III) dosage ratio on the structure and anion adsorptive removal of hydrothermally precipitated composites: Insights from EXAFS/XANES, XRD and FTIR.

    Science.gov (United States)

    Chubar, Natalia; Gerda, Vasyl; Banerjee, Dipanjan; Yablokova, Ganna

    2017-02-01

    In this work, we present material chemistry in the hydrothermal synthesis of new complex structure materials based on various dosage ratios of Fe and Ce (1:0, 2:1, 1:1, 1:2, 0:1), characterize them by the relevant methods that allow characterization of both crystalline and amorphous phases and correlate their structure/surface properties with the adsorptive performance of the five toxic anions. The applied synthesis conditions resulted in the formation of different compounds of Fe and Ce components. The Fe-component was dominated by various phases of Fe hydrous oxides, whereas the Ce-component was composed of various phases of Ce carbonates. The presence of two metal salts in raw materials resulted in the formation of a mesoporous structure and averaged the surface area compared to one metal-based material. The surface of all Fe-Ce composites was abundant in Fe component phases. Two-metal systems showed stronger anion removal performance than one-metal materials. The best adsorption was demonstrated by Fe-Ce based materials that had low crystallinity, that were rich in phases and that exhibited surfaces were abundant in greater number of surface functional groups. Notably, Fe extended fine structures simulated by EXAFS in these better adsorbents were rich from oscillations from both heavy and light atoms. This work provides new insights on the structure of composite inorganic materials useful to develop their applications in adsorption and catalysis. It also presents new inorganic anion exchangers with very high removal potential to fluoride and arsenate. Copyright © 2016 Elsevier Inc. All rights reserved.

  1. Effect of Fe(II)/Ce(III) dosage ratio on the structure and anion adsorptive removal of hydrothermally precipitated composites: Insights from EXAFS/XANES, XRD and FTIR

    KAUST Repository

    Chubar, Natalia

    2016-10-24

    In this work, we present material chemistry in the hydrothermal synthesis of new complex structure materials based on various dosage ratios of Fe and Ce (1:0, 2:1, 1:1, 1:2, 0:1), characterize them by the relevant methods that allow characterization of both crystalline and amorphous phases and correlate their structure/surface properties with the adsorptive performance of the five toxic anions. The applied synthesis conditions resulted in the formation of different compounds of Fe and Ce components. The Fe-component was dominated by various phases of Fe hydrous oxides, whereas the Ce-component was composed of various phases of Ce carbonates. The presence of two metal salts in raw materials resulted in the formation of a mesoporous structure and averaged the surface area compared to one metal-based material. The surface of all Fe-Ce composites was abundant in Fe component phases. Two-metal systems showed stronger anion removal performance than one-metal materials. The best adsorption was demonstrated by Fe-Ce based materials that had low crystallinity, that were rich in phases and that exhibited surfaces were abundant in greater number of surface functional groups. Notably, Fe extended fine structures simulated by EXAFS in these better adsorbents were rich from oscillations from both heavy and light atoms. This work provides new insights on the structure of composite inorganic materials useful to develop their applications in adsorption and catalysis. It also presents new inorganic anion exchangers with very high removal potential to fluoride and arsenate.

  2. Failure of composite wind turbine blade with hydrothermal effects%含温湿效应的复合材料风机叶片的破坏

    Institute of Scientific and Technical Information of China (English)

    王蔓; 白瑞祥; 李明颖; 沈亚南

    2012-01-01

    The gradual failure and failure mechanism of composite wind turbine blade applied to wind load and temperature-humidity load were studied by finite element numerical simulation for the early failure at different temperature and humidity. The wind turbine blade was reduced to cantilever model and the three-dimension model was conducted. The skin, web plate and the main beam were discrete by composite plate element. The three-dimension Hashin failure criterion of strain distribution was adopted for failure analysis. The stiffness and failure behavior of the wind blade structure were studied by using FEA software ABAQUS. The gradual failure and the effects on strength and stiffness of composite wind turbine blade were discussed under temperature and humidity load. The effects of hydrothermal of environment on material properties were widely obvious, which lead to the decrease of strength and stiffness of composite wind turbine.%针对复合材料风机叶片在温湿环境下的早期失效问题,采用有限元数值模拟方法研究了考虑了风载荷和温湿载荷共同作用下叶片的逐步破坏行为和破坏机理.将风机叶片简化为悬臂梁模型,进行了三维建模,对蒙皮、腹板和主梁均采用板壳单元进行离散,分别讨论了在不同温度及湿度条件下,环境因素对复合材料风机叶片材料性能的影响,并分析了叶片刚度、强度的变化及破坏情况.同时引入基于应变分布的三维Hashin失效准则,利用有限元分析软件ABAQUS对风机叶片进行刚度和破坏分析,讨论了风载下复合材料风机叶片的逐步破坏行为以及温湿载荷对风机叶片强度和刚度的影响.分析结果表明,高温湿润的环境对复合材料风机叶片材料性能影响很大,导致叶片的强度和刚度均有不同程度的降低.

  3. Poly(ε-caprolactone) reinforced with sol-gel synthesized organic-inorganic hybrid fillers as composite substrates for tissue engineering.

    Science.gov (United States)

    Russo, Teresa; Gloria, Antonio; D-Antò, Vincenzo; D'Amora, Ugo; Ametrano, Gianluca; Bollino, Flavia; De Santis, Roberto; Ausanio, Giovanni; Catauro, Michelina; Rengo, Sandro; Ambrosio, Luigi

    2010-01-01

    The importance of polymer-based composite materials to make multifunctional substrates for tissue engineering and the strategies to improve their performances have been stressed in the literature. Bioactive features of sol-gel synthesized poly(ε-caprolactone)/TiO₂ or poly(ε-caprolactone)/ZrO₂ organic-inorganic hybrid materials are widely documented. Accordingly, the aim of this preliminary research was to develop advanced composite substrates consisting of a poly(ε-caprolactone) matrix reinforced with sol-gel synthesized PCL/TiO₂ or PCL/ZrO₂ hybrid fillers. Micro-computed tomography and atomic force microscopy analyses allowed to study surface topography and roughness. On the other hand, mechanical and biological performances were evaluated by small punch tests and Alamar Blue™ assay, respectively. Micro-computed tomography and atomic force microscopy analyses highlighted the effect of the preparation technique. Results from small punch tests and Alamar Blue™ assay evidenced that PCL reinforced with Ti2 (PCL=12, TiO₂=88 wt%) and Zr2 (PCL=12, ZrO₂=88 wt%) hybrid fillers provided better mechanical and biological performances. PCL reinforced with Ti2 (PCL=12, TiO₂=88 wt%) and Zr2 (PCL=12, ZrO₂=88 wt%) hybrid fillers could be considered as advanced composite substrates for hard tissue engineering.

  4. Effect of Mo on Microstructures and Wear Properties of In Situ Synthesized Ti(C,N)/Ni-Based Composite Coatings by Laser Cladding.

    Science.gov (United States)

    Wu, Fan; Chen, Tao; Wang, Haojun; Liu, Defu

    2017-09-06

    Using Ni60 alloy, C, TiN and Mo mixed powders as the precursor materials, in situ synthesized Ti(C,N) particles reinforcing Ni-based composite coatings are produced on Ti6Al4V alloys by laser cladding. Phase constituents, microstructures and wear properties of the composite coatings with 0 wt % Mo, 4 wt % Mo and 8 wt % Mo additions are studied comparatively. Results indicate that Ti(C,N) is formed by the in situ metallurgical reaction, the (Ti,Mo)(C,N) rim phase surrounding the Ti(C,N) ceramic particle is synthesized with the addition of Mo, and the increase of Mo content is beneficial to improve the wear properties of the cladding coatings. Because of the effect of Mo, the grains are remarkably refined and a unique core-rim structure that is uniformly dispersed in the matrix appears; meanwhile, the composite coatings with Mo addition exhibit high hardness and excellent wear resistance due to the comprehensive action of dispersion strengthening, fine grain strengthening and solid solution strengthening.

  5. Synthesizing Nanomaterials for Energy Applications: Probing Activity as a Function of Composition, Morphology and Purity to Address Key Issues Associated with Fuel Cells and Li-Ion Batteries

    Science.gov (United States)

    Scofield, Megan Elaine

    With the growing need to find alternative clean energy sources to fossil fuels, research into developing efficient fuel cells and batteries stands at the forefront of this grand effort. However, before mass commercialization, fundamental key issues need to be addressed. For example, fuel cells are subject to high catalyst costs and poor durability of the underlying carbon support. As a way to alleviate these issues, we have synthesized ultrathin one-dimensional (1D) alloy nanowires to probe the effect of composition, purity, and one-dimensionality upon the observed overall activity, performance, and durability. In terms of chemical composition, crystalline ultrathin PtM alloy nanowires (NWs) ('M' = Fe, Co, Ru, Cu, and Au) were generated and subsequently evaluated for the hydrogen oxidation reaction (HOR). Additionally, ternary-based catalysts were synthesized (PtRuFe) in order to analyze how chemical composition influences CO tolerance as well as methanol oxidation reaction (MOR) and formic acid oxidation reaction (FAOR) activities. In both cases, we utilized a sustainably mild, ambient wet-synthesis method for the fabrication of chemically pure and crystalline systems in order to fabricate ultrathin, homogeneous alloy NWs. Moreover, in these studies, our NW systems exhibit favorable synergistic electronic effects with respect to controls. To address another fundamental issue associated with the durability of fuel cells, we have synthesized various metal oxide and perovskite materials of different sizes and chemical compositions as supports for Pt nanoparticles (NPs). Specifically, we have demonstrated favorable metal support interactions between the Pt NPs and the SrRuO3 NP supports, which lead to increased MOR activity as compared with not only the other metal oxide supports tested but also the commercial Pt NP/C standard. In terms of Li-ion batteries, LiFePO4 materials have become increasingly popular as a cathode material due to the many benefits they possess

  6. A highly stable (SnOx-Sn)@few layered graphene composite anode of sodium-ion batteries synthesized by oxygen plasma assisted milling

    Science.gov (United States)

    Cheng, Deliang; Liu, Jiangwen; Li, Xiang; Hu, Renzong; Zeng, Meiqing; Yang, Lichun; Zhu, Min

    2017-05-01

    The (SnOx-Sn)@few layered graphene ((SnOx-Sn)@FLG) composite has been synthesized by oxygen plasma-assisted milling. Owing to the synergistic effect of rapid plasma heating and ball mill grinding, SnOx (1 ≤ x ≤ 2) nanoparticles generated from the reaction of Sn with oxygen are tightly wrapped by FLG nanosheets which are simultaneously exfoliated from expanded graphite, forming secondary micro granules. Inside the granules, the small size of the SnOx nanoparticles enables the fast kinetics for Na+ transfer. The in-situ formed FLG and residual Sn nanoparticles improve the electrical conductivity of the composite, meanwhile alleviate the aggregation of SnOx nanoparticles and relieve the volume change during the cycling, which is beneficial for the cyclic stability for the Na+ storage. As an anode material for sodium-ion batteries, the (SnOx-Sn)@FLG composite exhibits a high reversible capacity of 448 mAh g-1 at a current density of 100 mA g-1 in the first cycle, with 82.6% capacity retention after 250 cycles. Even when the current density increases to 1000 mA g-1, this composite retains 316.5 mAh g-1 after 250 cycles. With superior Na+ storage stability, the (SnOx-Sn)@FLG composite can be a promising anode material for high performance sodium-ion batteries.

  7. Characterisation and thermal properties of titanium dioxide nanoparticles-containing biodegradable polylactide composites synthesized by sol-gel method.

    Science.gov (United States)

    Mhlanga, Nikiwe; Ray, Suprakas Sinha

    2014-06-01

    This study reports the synthesis, characterisation and thermal properties of polylactide (PLA)/titanium dioxide nanoparticles (TiO2 NPs) composites using the sol-gel method. The percentage weight of TiO2 NP sol was varied from 3, 8, 11 and 14. The synthesised composites were characterised using scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction, energy dispersive X-ray spectroscopy (EDS), thermogravimetric analysis and dynamic mechanical analysis. Encapsulation of the TiO2 into the PLA matrix was attainable based on the SEM images and the FTIR and EDS results. The thermal stability of the composites was shifted to lower temperatures due to photodegradation induced by the metal oxide on the PLA chain. Both PLA and TiO2 NPs have potential in drug delivery because of their biocompatibility and biodegradability.

  8. Supramolecular network formed through O-H$\\cdots$O and - stacking interactions: Hydrothermal syntheses and crystal structures of M(H2O)6](optp)2 (M = Mg, Ni, Zn, and optp = 1-oxopyridinium-2-thiopropionate)

    Indian Academy of Sciences (India)

    Murugan Indrani; Ramasamy Ramasubramanian; Frank R Fronczek; Dario Braga; N Y Vasanthacharya; Sudalaiandi Kumaresan

    2009-07-01

    A novel class of complexes of the type [M(H2O)6](optp)2 (where M = Mg, Ni, Zn, and optp = 1-oxopyridinium-2-thiopropionate) were prepared hydrothermally from metal acetates and 1-oxopyridinium-2-thiopropionic acid (Hoptp), and structurally characterized by X-ray diffraction. Complexes [Mg(H2O)6](optp)2 (1), [Ni(H2O)6](optp)2 (2) and [Zn(H2O)6](optp)2 (3) have isomorphic structures, consisting of one [M(H2O)6]2+ cation and two anions of Hoptp, which are linked through hydrogen bonding to form extended networks. In each case, the metal cation sits on a crystallographic centre of inversion and binds to six water molecules. The organic anions form a one-dimensional chain with the hexaaquametal(II) moieties via hydrogen bonds.

  9. Effect of Fe2P in LiFePO4/Fe2P composite on electrochemical properties synthesized by MA and control of heat condition

    Institute of Scientific and Technical Information of China (English)

    PARK Jong Suk; LEE Kyung Tae; LEE Kyung Sub

    2006-01-01

    In order to control the size and distribution of the high conductive Fe2P in LiFePO4/Fe2P composite, two different cooling rates (Fast: 15 ℃·min-1, Slow: 2 ℃·min-1) were employed after mechanical alloying.The discharge capacity of the fast cooled was 83 mAh·g-1 and the slow cooled 121 mAh·g-1.The particle size of the synthesized powder was examined by transmission electron microscopy and distribution of Fe2P was characterized using scanning electron microscopy (SEM).In addition, two-step heat treatment was carried out for better distribution of Fe2P.X-ray diffraction (XRD) and Rietveld refinement reveal that LiFePO4/Fe2P composite consists of 95.77% LiFePO4 and 4.33% of Fe2P.

  10. Chemical composition of deep hydrothermal fluids in the Ribeira Grande geothermal field (São Miguel, Azores)

    Science.gov (United States)

    Carvalho, M. R.; Forjaz, V. H.; Almeida, C.

    2006-08-01

    The Ribeira Grande geothermal field is a water-dominated geothermal system, located within Água de Pau/Fogo Volcano in the central part of the São Miguel Island. This geothermal system is exploited for energy production by wells sustaining two power plants. The wells produce from a formation of pillow lavas divided into different aquifers, with a fairly isothermal zone from 800 to 1300 m in depth, where reservoir temperature reaches 230 to 245 °C. Below the depth of 1300 m there is a slight temperature reversal. The fluid produced has excess enthalpy and, separated at atmospheric pressure, is characterized by mineralization of sodium-chloride type up to 6-7 g/l, the concentration of dissolved silica varies between 450 and 650 mg/l and the pH ranges between 8 and 8.6. The gas phase is dominantly CO 2, at a concentration of 98% of NCG. The composition of the deep geothermal fluid was obtained by computer simulation, using the WATCH program, and was compared with the composition of the bottom-hole samples. The approximations, in this simulation, were considered the single- and multi-step steam separation. The reference temperatures were based on: (i) the measured temperature in wells; (ii) the Na/K geothermometric temperature and (iii) the enthalpy-saturation temperature. According to both the measured and geothermometric temperatures, the deep fluid of the wells has two phases with a steam fraction up to 0.34, at higher well discharges. The measured enthalpy is always greater than the calculated enthalpy. The calcite equilibrium indicates scaling, since the fluid is flashing, around 2.28 mg/l CaCO 3 at the maximum discharge. The geothermal wells exploit three different aquifers, the lower of which is liquid and slightly colder than the upper ones. The intermediate is a two-phase aquifer with a steam fraction up to 0.081. The upper aquifer is probably of steam phase. The main differences between the aquifers are the temperature and boiling; both enthalpy and

  11. Characterisation and thermal properties of titanium dioxide nanoparticles-containing biodegradable polylactide composites synthesized by sol–gel method

    CSIR Research Space (South Africa)

    Mhlanga, N

    2014-01-01

    Full Text Available mechanical analysis. Encapsulation of the TiO(sub2) into the PLA matrix was attainable based on the SEM images and the FTIR and EDS results. The thermal stability of the composites was shifted to lower temperatures due to photodegradation induced by the metal...

  12. Effect of different oxidants on polyaniline/single walled carbon nanotubes composites synthesized via ultrasonically initiated in-situ chemical polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Gull, Nafisa, E-mail: gullchemist@gmail.com [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan); Khan, Shahzad Maqsood, E-mail: shahzadkhan81@hotmail.com [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan); Islam, Atif; Zia, Saba; Shafiq, Muhammad; Sabir, Aneela; Munawar, Muhammad Azeem [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan); Butt, Muhammad Taqi Zahid [College of Engineering and Emerging Technologies, University of the Punjab, Lahore, 54590 (Pakistan); Jamil, Tahir [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan)

    2016-04-01

    This study is aimed at investigating the effect of different oxidants on properties of polyaniline/single walled carbon nanotubes (PANI/SWCNT) composites and scrutinizing a suitable oxidant to improve the properties of composites. PANI/SWCNT composites were fabricated via ultrasonically initiated in-situ chemical polymerization technique using four different oxidants; hydrogen peroxide (H{sub 2}O{sub 2}), ammonium peroxidisulphate ((NH{sub 4}){sub 2}S{sub 2}O{sub 8}), potassium dichromate (K{sub 2}Cr{sub 2}O{sub 7}) and potassium iodate (KIO{sub 3}). Percent yield (97%), molecular weight (45532 g mol{sup −1}) and electrical conductivity (0.835 S cm{sup −1}) were found maximum for composite prepared in the presence of H{sub 2}O{sub 2}. Structural confirmation of PANI and charge transfer complex formation between PANI and SWCNT were confirmed by fourier transform infrared spectroscopy, UV–visible spectroscopy and X-ray diffraction spectroscopy. Thermogravimetric analysis verified that the PANI/SWCNT composite synthesized using H{sub 2}O{sub 2} had maximum thermal stability with least thermal degradation (∼28%). Minimal thermal transitions of the composite were also observed for same composite by differential scanning calorimetry. Scanning electron microscopic images of PANI/SWCNT composites revealed that SWCNT were properly dispersed in PANI matrix when H{sub 2}O{sub 2} was used. Above results provide the valuable suggestion that; H{sub 2}O{sub 2} is a promising oxidant to enhance structural, thermal, electrical and microscopic properties of composites. - Highlights: • Ultrasonically initiated in-situ chemical polymerization protocol was devised for synthesis of PANI/SWCNT composites. • SEM micrographs of PANI/SWCNT-1 showed uniform dispersed structure. • Better thermal stability and conductivity was evidenced for H{sub 2}O{sub 2} based PANI/SWCNT composite. • π–π interaction between PANI and SWCNT is confirmed by FTIR and UV

  13. Hydrothermally grown and self-assembled modified titanium and nickel oxide composite nanosheets on Nitinol-based fibers for efficient solid phase microextraction.

    Science.gov (United States)

    Wang, Huiju; Song, Wenlan; Zhang, Min; Zhen, Qi; Guo, Mei; Zhang, Yida; Du, Xinzhen

    2016-10-14

    A novel titanium and nickel oxide composite nanosheets (TiO2/NiOCNSs) coating was in situ grown on a Nitinol (NiTi) wire by direct hydrothermal treatment and modified by self-assembly of trichlorophenylsilane for solid phase microextraction (SPME). TiO2/NiOCNSs were radially oriented and chemically bonded to the NiTi substrate with double-faced open access sites. Moreover the phenyl modified TiO2/NiOCNSs (TiO2/NiOCNSs-Ph) coating exhibited original surface supporting framework favorable for effective SPME. The extraction performance of TiO2/NiOCNSs-Ph coated NiTi (NiTi-TiO2/NiOCNSs-Ph) fiber was investigated for the concentration and detection of ultraviolet (UV) filters, polycyclic aromatic hydrocarbons (PAHs), phthalate acid esters and polychlorinated biphenyls coupled to HPLC with UV detection. The novel fiber exhibited better selectivity for UV filters and PAHs and presented greater extraction capability compared to commercial polydimethylsiloxane and polyacrylate fibers. Under the optimized conditions for SPME of UV filters, the proposed method presented linear ranges from 0.1 to 300μg/L with correlation coefficients of higher than 0.999 and limits of detection from 0.030μg/L to 0.064μg/L. Relative standard deviations (RSDs) were below 7.16% and 8.42% for intra-day and inter-day measurements with the single fiber, respectively. Furthermore RSDs for fiber-to-fiber reproducibility from 6.57% to 8.93% were achieved. The NiTi-TiO2/NiOCNSs-Ph fiber can be used up to 200 times. The proposed method was successfully applied to the preconcentration and determination of trace target UV filters in different environmental water samples. The relative recoveries from 87.3% to 104% were obtained with RSDs less than 8.7%.

  14. Hydrothermal Formation of Lath-Shaped Trioctahedral Smectite with High Crystallinity

    Institute of Scientific and Technical Information of China (English)

    Hirohisa YAMADA; Kenji TAMURA; Shingo YOKOYAMA; Yujiro WATANABE

    2006-01-01

    Lath-shaped and highly crystalline trioctahedral smectites were synthesized under hydrothermal conditions. The quenched glasses with stoichiometrically dehydrated Na-smectite compositions were treated at (a) 500℃ and 100 MPa for 1 and 11 days; and (b) 300℃ and 100 MPa for 7 days. The crystallinity and particle size of products were dependent on the chemical composition of the starting glass, synthetic temperature and duration of hydrothermal treatment. The high structural ordering and large dimensions of the products were confirmed from the sharpness of XRD peaks; and hydration behavior under controlled relative humidity. Transmission electron microscopy was also performed for the characterization of the particle size of product. Particle sizes vary from ca. 10 nm to a few μm by changing the chemical compositions of the starting materials. The product with the highest structural ordering and largest dimension was obtained from Na0.33(Mg1.83Al0.67)Si4O11 glass treated at 500℃ and 100 MPa for 1 day. The obtained results also confirmed the metastability and compositional dependency in the formation of highly crystalline trioctahedral smectite at hydrothermal conditions.

  15. Microsized Porous SiOx@C Composites Synthesized through Aluminothermic Reduction from Rice Husks and Used as Anode for Lithium-Ion Batteries.

    Science.gov (United States)

    Cui, Jinlong; Cui, Yongfu; Li, Shaohui; Sun, Hongliang; Wen, Zhongsheng; Sun, Juncai

    2016-11-09

    Microsized porous SiOx@C composites used as anode for lithium-ion batteries (LIBs) are synthesized from rice husks (RHs) through low-temperature (700 °C) aluminothermic reduction. The resulting SiOx@C composite shows mesoporous irregular particle morphology with a high specific surface area of 597.06 m(2)/g under the optimized reduction time. This porous SiOx@C composite is constructed by SiOx nanoparticles uniformly dispersed in the C matrix. When tested as anode material for LIBs, it displays considerable specific capacity (1230 mAh/g at a current density of 0.1 A/g) and excellent cyclic stability with capacity fading of less than 0.5% after 200 cycles at 0.8 A/g. The dramatic volume change for the Si anode during lithium-ion (Li(+)) insertion and extraction can be successfully buffered because of the formation of Li2O and Li4SiO4 during initial lithiation process and carbon coating layer on the surface of SiOx. The porous structure could also mitigate the volume change and mechanical strains and shorten the Li(+) diffusion path length. These characteristics improve the cyclic stability of the electrode. This low-cost and environment-friendly SiOx@C composite anode material exhibits great potential as an alternative for traditional graphite anodes.

  16. Facile in situ solvothermal method to synthesize MWCNT/SnIn{sub 4}S{sub 8} composites with enhanced visible light photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Chaoying; Tian, Li [Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164 (China); College of Hua Loogeng, Changzhou University, Changzhou 213164 (China); Liu, Bo; Liang, Qian [Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164 (China); Li, Zhongyu, E-mail: zhongyuli@mail.tsinghua.edu.cn [Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164 (China); College of Hua Loogeng, Changzhou University, Changzhou 213164 (China); Key Laboratory of Regional Environment and Ecoremediation (Ministry of Education), Shenyang University, Shenyang 110044 (China); Xu, Song [Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164 (China); Liu, Qiaoli; Lu, Dayong [Department of Materials Science and Engineering, Jilin Institute of Chemical Technology, Jilin 132022 (China)

    2015-06-05

    Highlights: • MWCNT/SnIn{sub 4}S{sub 8} composites were facilely fabricated via in situ solvothermal method. • MWCNT/SnIn{sub 4}S{sub 8} composites exhibited significantly enhanced visible-light activity. • MWCNT/SnIn{sub 4}S{sub 8} composites showed remarkable visible light photocatalytic activity. • MWCNT/SnIn{sub 4}S{sub 8} composites exhibited excellent photo-stability. • Possible photocatalytic mechanism under visible-light irradiation was proposed. - Abstract: Superior photocatalytic activity could be achieved by multi-walled carbon nanotube (MWCNT) incorporated in the porous assembly of marigold-like SnIn{sub 4}S{sub 8} heterostructures synthesized by a flexible in-situ solvothermal method. The as-prepared MWCNT/SnIn{sub 4}S{sub 8} composites were well-characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM) and UV–vis diffuse reflectance spectroscopy (DRS). The photocatalytic properties of the as-prepared samples were tested by photo-degradation of aqueous malachite green (MG) under the irradiation of visible light. It was found that the MWCNT/SnIn{sub 4}S{sub 8} composites showed enhanced visible light photocatalytic activity for dye degradation, and an optimum photocatalytic activity was observed over 3.0 wt.% MWCNT incorporated SnIn{sub 4}S{sub 8} composites. The superior photocatalytic activity of MWCNT/SnIn{sub 4}S{sub 8} composites could be ascribed to the existence of MWCNT which could serve as a good electron acceptor, mediator as well as the co-catalyst for dye degradation. The synergistic effect between SnIn{sub 4}S{sub 8} and MWCNT in the composites facilitated the interfacial charge transfer driven by the excitation of SnIn{sub 4}S{sub 8} under visible-light irradiation. Furthermore, a possible mechanism for the photocatalytic degradation of MWCNT/SnIn{sub 4}S{sub 8} composites was also discussed.

  17. Zinc stannate nanostructures: hydrothermal synthesis

    Directory of Open Access Journals (Sweden)

    Sunandan Baruah and Joydeep Dutta

    2011-01-01

    Full Text Available Nanostructured binary semiconducting metal oxides have received much attention in the last decade owing to their unique properties rendering them suitable for a wide range of applications. In the quest to further improve the physical and chemical properties, an interest in ternary complex oxides has become noticeable in recent times. Zinc stannate or zinc tin oxide (ZTO is a class of ternary oxides that are known for their stable properties under extreme conditions, higher electron mobility compared to its binary counterparts and other interesting optical properties. The material is thus ideal for applications from solar cells and sensors to photocatalysts. Among the different methods of synthesizing ZTO nanostructures, the hydrothermal method is an attractive green process that is carried out at low temperatures. In this review, we summarize the conditions leading to the growth of different ZTO nanostructures using the hydrothermal method and delve into a few of its applications reported in the literature.

  18. Variations in the chemical and stable isotope composition of carbon and sulfur species during organic-rich sediment alteration: An experimental and theoretical study of hydrothermal activity at guaymas basin, gulf of california

    Science.gov (United States)

    Seewald, Jeffrey S.; Seyfried, W.E.; Shanks, Wayne C.

    1994-01-01

    Organic-rich diatomaceous ooze was reacted with seawater and a Na-Ca-K-Cl fluid of seawater chlorinity at 325-400??C, 400-500 bars, and fluid/sediment mass ratios of 1.56-2.35 to constrain factors regulating the abundance and stable isotope composition of C and S species during hydrothermal alteration of sediment from Guaymas Basin, Gulf of California. Alteration of inorganic and organic sedimentary components resulted in extensive exchange reactions, the release of abundant H2S, CO2, CH4, and Corganic, to solution, and recrystallization of the sediment to an assemblage containing albitic plagioclase, quartz, pyrrhotite, and calcite. The ??34Scdt values of dissolved H2S varied from -10.9 to +4.3??? during seawater-sediment interaction at 325 and 400??C and from -16.5 to -9.0??? during Na-Ca-K-Cl fluid-sediment interaction at 325 and 375??C. In the absence of seawater SO4, H2S is derived from both the transformation of pyrite to pyrrhotite and S released during the degradation of organic matter. In the presence of seawater SO4, reduction of SO4 contributes directly to H2S production. Sedimentary organic matter acts as the reducing agent during pyrite and SO4 reduction. Requisite acidity for the reduction of SO4 is provided by Mg fixation during early-stage sediment alteration and by albite and calcite formation in Mg-free solutions. Organically derived CH4 was characterized by ??13Cpdb values ranging between -20.8 and -23.1???, whereas ??13Cpdb values for dissolved Corganic ranged between -14.8 and -17.7%. Mass balance calculations indicate that ??13C values for organically derived CO2 were ??? - 14.8%. Residual solid sedimentary organic C showed small (??? 0.7???) depletions in 13C relative to the starting sediment. The experimental results are consistent with the isotopic and chemical composition of natural hydrothermal fluids and minerals at Guaymas Basin and permit us to better constrain sources and sinks for C and S species in subseafloor hydrothermal systems

  19. Variations in the chemical and stable isotope composition of carbon and sulfur species during organic-rich sediment alteration: An experimental and theoretical study of hydrothermal activity at guaymas basin, gulf of california

    Science.gov (United States)

    Seewald, Jeffrey S.; Seyfried, William E., Jr.; Shanks, Wayne C., III

    1994-11-01

    Organic-rich diatomaceous ooze was reacted with seawater and a Na-Ca-K-Cl fluid of seawater chlorinity at 325-400°C, 400-500 bars, and fluid/sediment mass ratios of 1.56-2.35 to constrain factors regulating the abundance and stable isotope composition of C and S species during hydrothermal alteration of sediment from Guaymas Basin, Gulf of California. Alteration of inorganic and organic sedimentary components resulted in extensive exchange reactions, the release of abundant H 2S, CO 2, CH 4, and C organic, to solution, and recrystallization of the sediment to an assemblage containing albitic plagioclase, quartz, pyrrhotite, and calcite. The δ 34S cdt values of dissolved H 2S varied from -10.9 to +4.3‰ during seawater-sediment interaction at 325 and 400°C and from -16.5 to -9.0‰ during Na-Ca-K-Cl fluid-sediment interaction at 325 and 375°C. In the absence of seawater SO 4, H 2S is derived from both the transformation of pyrite to pyrrhotite and S released during the degradation of organic matter. In the presence of seawater SO 4, reduction of SO 4 contributes directly to H 2S production. Sedimentary organic matter acts as the reducing agent during pyrite and SO 4 reduction. Requisite acidity for the reduction of SO 4 is provided by Mg fixation during early-stage sediment alteration and by albite and calcite formation in Mg-free solutions. Organically derived CH 4 was characterized by δ 13C pdb values ranging between -20.8 and -23.1‰, whereas δ 13C pdb values for dissolved C organic ranged between -14.8 and -17.7%. Mass balance calculations indicate that δ13C values for organically derived CO 2 were ≥ - 14.8%. Residual solid sedimentary organic C showed small (≤ 0.7‰) depletions in 13C relative to the starting sediment. The experimental results are consistent with the isotopic and chemical composition of natural hydrothermal fluids and minerals at Guaymas Basin and permit us to better constrain sources and sinks for C and S species in subseafloor

  20. Catastrophic volcanic collapse: relation to hydrothermal processes.

    Science.gov (United States)

    López, D L; Williams, S N

    1993-06-18

    Catastrophic volcanic collapse, without precursory magmatic activity, is characteristic of many volcanic disasters. The extent and locations of hydrothermal discharges at Nevado del Ruiz volcano, Colombia, suggest that at many volcanoes collapse may result from the interactions between hydrothermal fluids and the volcanic edifice. Rock dissolution and hydrothermal mineral alteration, combined with physical triggers such as earth-quakes, can produce volcanic collapse. Hot spring water compositions, residence times, and flow paths through faults were used to model potential collapse at Ruiz. Caldera dimensions, deposits, and alteration mineral volumes are consistent with parameters observed at other volcanoes.

  1. Polyaniline – Carrageenan - Polyvinyl Alcohol Composite Material Synthesized Via Interfacial Polymerization, its Morphological Characteristics and Enhanced Solubility in Water

    Science.gov (United States)

    Montalbo, R. C. K.; Marquez, M. C.

    2017-09-01

    In recent years, conducting polyaniline (PAni) has been a popular interest of research in the field of conducting polymers due to its relatively low cost, ease of production, good conductivity, and environmental stability. Many studies however, have focused on improving its short-comings such as its limited processability and solubility in common solvents. In this study, PAni, soluble in water was produced via interfacial polymerization with chloroform as the organic solvent. Poly(vinyl alcohol) (PVA) and kappa(κ), iota(ι) and lambda(λ) - carrageenan (κCGN, ιCGN, λCGN) were added to the aqueous layer to stabilize PAni in the medium. FTIR and UV-Vis absorption spectra of the solutions as well as the fabricated film confirmed the existence of PAni emeraldine salt (PAni-ES). FTIR spectrum also confirmed the peaks corresponding to the interaction of PAni with the CGNs. Moreover, PVA-CGN played a very large role on the stability of the PAni nanofibers integrated on the PVA-CGN matrix. The morphologies of the products were further investigated using SEM and TEM. Polymer electrolyte for supercapacitor or an interfacial layer for organic solar cell is being targeted as potential application of the synthesized water soluble PAni.

  2. Isotopic composition of Murchison organic compounds: Intramolecular carbon isotope fractionation of acetic acid. Simulation studies of cosmochemical organic syntheses

    Science.gov (United States)

    Yuen, G. U.; Cronin, J. R.; Blair, N. E.; Desmarais, D. J.; Chang, S.

    1991-01-01

    Recently, in our laboratories, samples of Murchison acetic acid were decarboxylated successfully and the carbon isotopic composition was measured for the methane released by this procedure. These analyses showed significant differences in C-13/C-12 ratios for the methyl and carboxyl carbons of the acetic acid molecule, strongly suggesting that more than one carbon source may be involved in the synthesis of the Murchison organic compounds. On the basis of this finding, laboratory model systems simulating cosmochemical synthesis are being studied, especially those processes capable of involving two or more starting carbon sources.

  3. Hydrothermal syntheses and characterization of two novel luminescent Cadmium(II) frameworks: From 1D infinite triple Cd-(trz)-Cd bridges to a rare I2O0 network with 2D Cd-Br-Cd inorganic connectivity

    Science.gov (United States)

    Liu, Shi Xin; Li, Jian Hui; Wang, You You; Wu, Xiang Xia; Huo, Jian Zhong; Ding, Bin; Wang, Xiu Guang; Zhu, Zhao Zhou; Xia, Jun

    2015-05-01

    Using the 4-substituted-1,2,4-triazole derivate ligand 4-p-tolyl-1,2,4-triazole (L), two novel luminescent Cadmium(II) frameworks, namely {[Cd(μ2-L)3]·(NO3)2·L}n (1) and [Cd1.5(μ2-L)(μ2-Br)2(μ3-Br)]n (2) have been isolated under hydrothermal conditions. The structural analysis reveals that 1 presents a one-dimensional (1D) chain structural motif containing novel infinite triple Cd-(trz)-Cd bridges (triply trz-bridged M-M species). While 2 presents a rare I2O0 type framework, in which the infinite 2D Cd-Br-Cd inorganic connectivity with a 4-connected Kagome topology can be observed. The FT-IR, PXRD and thermal stabilities of 1-2 have investigated. The solid-state photo-luminescent spectra of organic ligand L and 1-2 also have been measured indicating strong emission bands.

  4. Structure and composition of Zn(x)Cd(1-xS) films synthesized through chemical bath deposition.

    Science.gov (United States)

    Tosun, B Selin; Pettit, Chelsea; Campbell, Stephen A; Aydil, Eray S

    2012-07-25

    Zinc cadmium sulfide (ZnxCd1-xS) thin films grown through chemical bath deposition are used in chalcopyrite solar cells as the buffer layer between the n-type zinc oxide and the p-type light absorbing chalcopyrite film. To optimize energetic band alignment and optical absorption, advanced solar cell architectures require the ability to manipulate x as a function of distance from the absorber-ZnCdS interface. Herein, we investigate the fundamental factors that govern the evolution of the composition as a function of depth in the film. By changing the initial concentrations of Zn and Cd salts in the bath, the entire range of overall compositions ranging from primarily cubic ZnS to primarily hexagonal CdS could be deposited. However, films are inhomogeneous and x varies significantly as function of distance from the film-substrate interface. Films with high overall Zn concentration (x > 0.5) exhibit a Cd-rich layer near the film-substrate interface because Cd is more reactive than Zn. This layer is typically beneath a nearly pure ZnS film that forms after the Cd-rich layers are deposited and Cd is depleted in the bath. In films with high overall Cd concentration (x < 0.5) the Zn concentration rises towards the film's surface. Fortunately, these gradients are favorable for solar cells based on low band gap chalcopyrite films.

  5. Structure and Mechanical Properties of Ni-P-Nano Al2O3 Composite Coatings Synthesized by Electroless Plating

    Institute of Scientific and Technical Information of China (English)

    ZHOU Guang-hong; DING Hong-yan; ZHOU Fei; ZHANG Yue

    2008-01-01

    Ni-P-nano Al2O3 composite coatings were deposited by electroless plating, and their microstructures were observed by SEM (scanning electron microscope). The microhardness and the wear resistance of the Ni-P-nano Al2O3 composite coatings were measured using microhardness tester and block-on-ring tribometer, respectively, and the comparison with those of Ni-P coatings or Ni-P-micro Al2O3 coating was given. The influences of aging temperature on their hardness and wear resistance were analyzed. The results showed that the nano Al2O3 particles were distributed uniformly in the Ni-P-Al2O3 coatings. Among three kinds of Ni-P based coatings, the hardness and wear resistance of Ni-P-nano Al2O3 coatings were largest, and the maximum values could be obtained at 400 ℃. This indicated that the precipitation of nano Al2O3 particles would improve the hardness and wear resistance of the Ni-P coatings.

  6. Co-synthesized Y-stabilized Bi2O3 and Sr-substituted LaMnO3 composite anode for high performance solid oxide electrolysis cell

    Science.gov (United States)

    Yan, Jingbo; Zhao, Zhe; Shang, Lei; Ou, Dingrong; Cheng, Mojie

    2016-07-01

    In this study we report a nano-composite anode comprised of Y-stabilized Bi2O3 (YSB) and Sr-substituted LaMnO3 (LSM) for solid oxide electrolysis cell (SOEC). The composite powder with primary particle size ranging from 20 to 80 nm is co-synthesized via a simple citric-nitrate combustion method. X-ray diffraction examination confirms cubic fluorite YSB and rhombohedral perovskite LSM as the main phases in the composite. Temperature programmed O2 desorption identifies remarkable low temperature desorption at 330 °C. Similarly, temperature programmed H2 reduction reveals strong reduction at 385 °C. The facile oxygen evolution on YSB-LSM may result from the increased amount of oxygen vacancies and improved oxygen ion mobility. A cell employing YSB-LSM composite anode achieves current density of -1.52 A cm-2 at 800 °C and 1.28 V, 50% higher than conventional LSM-YSZ cell. Impedance results and analysis of distribution of relaxation times indicate that the rate-determining anode processes are effectively accelerated on YSB-LSM. The activation energy for oxygen evolution reaction on YSB-LSM is reduced to 0.65 eV, notably lower than on LSM-YSZ (1.29 eV). The high performance of YSB-LSM composite anode is attributed to the fast ion decorporation on YSB, the facile O2 formation on LSM, and the abundant phase boundaries that facilitate the two processes.

  7. One-pot route to synthesize SnO2-Reduced graphene oxide composites and their enhanced electrochemical performance as anodes in lithium-ion batteries

    Science.gov (United States)

    Li, Wenying; Yoon, Dohyeon; Hwang, Jieun; Chang, Wonyoung; Kim, Jaehoon

    2015-10-01

    A simple, one-pot route was developed for the synthesis of SnO2-reduced graphene oxide (RGO) composites. Simultaneous reduction of graphene oxide (GO) and heterogeneous nucleation and growth of SnO2 on the surface of RGO under the supercritical methanol medium resulted in uniform deposition of well-dispersed SnO2 nanoparticles on the RGO sheets. In comparison with the bare SnO2 nanoparticles and bare RGO sheets, the as-synthesized SnO2-RGO composites exhibited enhanced Li-ion storage and high rate performance. The SnO2-RGO composite with a SnO2 loading of 58 wt% delivered a reversible discharge capacity of 776 mAh g-1 after 70 cycles at a current density of 0.1 A g-1 and a rate performance of 147 mAh g-1 at a high current density of 5 A g-1. In addition, after 1000 continuous cycles at 1 A g-1, the composite electrode exhibited a reversible discharge capacity as high as 531 mAh g-1 with excellent capacity retention. The enhanced long-term cyclability and high-rate performance of the SnO2-RGO composite can be attributed to the effective confinement of SnO2 nanoparticles on the RGO sheets, and thus, the interparticle agglomeration and volume change associated with alloying-dealloying of SnO2 during cycling can be prevented and cell integrity can be maintained.

  8. Optimization of Hydrothermal and Diluted Acid Pretreatments of Tunisian Luffa cylindrica (L.) Fibers for 2G Bioethanol Production through the Cubic Central Composite Experimental Design CCD: Response Surface Methodology

    Science.gov (United States)

    Ziadi, Manel; Ben Hassen-Trabelsi, Aida; Mekni, Sabrine; Aïssi, Balkiss; Alaya, Marwen; Bergaoui, Latifa; Hamdi, Moktar

    2017-01-01

    This paper opens up a new issue dealing with Luffa cylindrica (LC) lignocellulosic biomass recovery in order to produce 2G bioethanol. LC fibers are composed of three principal fractions, namely, α-cellulose (45.80%  ± 1.3), hemicelluloses (20.76%  ± 0.3), and lignins (13.15%  ± 0.6). The optimization of LC fibers hydrothermal and diluted acid pretreatments duration and temperature were achieved through the cubic central composite experimental design CCD. The pretreatments optimization was monitored via the determination of reducing sugars. Then, the 2G bioethanol process feasibility was tested by means of three successive steps, namely, LC fibers hydrothermal pretreatment performed at 96°C during 54 minutes, enzymatic saccharification carried out by means of a commercial enzyme AP2, and the alcoholic fermentation fulfilled with Saccharomyces cerevisiae. LC fibers hydrothermal pretreatment liberated 33.55 g/kg of reducing sugars. Enzymatic hydrolysis allowed achieving 59.4 g/kg of reducing sugars. The conversion yield of reducing sugar to ethanol was 88.66%. After the distillation step, concentration of ethanol was 1.58% with a volumetric yield about 70%. PMID:28243606

  9. Optimization of Hydrothermal and Diluted Acid Pretreatments of Tunisian Luffa cylindrica (L. Fibers for 2G Bioethanol Production through the Cubic Central Composite Experimental Design CCD: Response Surface Methodology

    Directory of Open Access Journals (Sweden)

    Kaouther Zaafouri

    2017-01-01

    Full Text Available This paper opens up a new issue dealing with Luffa cylindrica (LC lignocellulosic biomass recovery in order to produce 2G bioethanol. LC fibers are composed of three principal fractions, namely, α-cellulose (45.80%  ± 1.3, hemicelluloses (20.76%  ± 0.3, and lignins (13.15%  ± 0.6. The optimization of LC fibers hydrothermal and diluted acid pretreatments duration and temperature were achieved through the cubic central composite experimental design CCD. The pretreatments optimization was monitored via the determination of reducing sugars. Then, the 2G bioethanol process feasibility was tested by means of three successive steps, namely, LC fibers hydrothermal pretreatment performed at 96°C during 54 minutes, enzymatic saccharification carried out by means of a commercial enzyme AP2, and the alcoholic fermentation fulfilled with Saccharomyces cerevisiae. LC fibers hydrothermal pretreatment liberated 33.55 g/kg of reducing sugars. Enzymatic hydrolysis allowed achieving 59.4 g/kg of reducing sugars. The conversion yield of reducing sugar to ethanol was 88.66%. After the distillation step, concentration of ethanol was 1.58% with a volumetric yield about 70%.

  10. Radiochromic film for dosimetric measurements in radiation shielding composites synthesized for applied in radiology procedures of high dose

    Energy Technology Data Exchange (ETDEWEB)

    Fontainha, C. C. P. [Universidade Federal de Minas Gerais, Departamento de Engenharia Nuclear, Av. Pte. Antonio Carlos 6627, 31270-901 Belo Horizonte, Minas Gerais (Brazil); Baptista N, A. T.; Faria, L. O., E-mail: crissia@gmail.com [Centro de Desenvolvimento da Tecnologia Nuclear / CNEN, Av. Pte. Antonio Carlos 6627, 31270-901 Belo Horizonte, Minas Gerais (Brazil)

    2015-10-15

    Full text: Medical radiology offers great benefit to patients. However, although specifics procedures of high dose, as fluoroscopy, Interventional Radiology, Computed Tomography (CT) make up a small percent of the imaging procedures, they contribute to significantly increase dose to population. The patients may suffer tissue damage. The probability of deterministic effects incidence depends on the type of procedure performed, exposure time, and the amount of applied dose at the irradiated area. Calibrated radiochromic films can identify size and distribution of the radiated fields and measure intensities of doses. Radiochromic films are sensitive for doses ranging from 0.1 to 20 c Gy and they have the same response for X-rays effective energies ranging from 20 to 100 keV. New radiation attenuators materials have been widely investigated resulting in dose reduction entrance skin dose. In this work, Bi{sub 2}O{sub 3} and ZrO{sub 2}:8 % Y{sub 2}O{sub 3} composites were obtained by mixing them with P(VDF-Tr Fe) copolymers matrix from casting method and then characterized by Ftir. Dosimetric measurements were obtained with Xr-Q A2 Gafchromic radiochromic films. In this setup, one radiochromic film is directly exposed to the X-rays beam and another one measures the attenuated beam were exposed to an absorbed dose of 10 mGy of RQR5 beam quality (70 kV X-ray beam). Under the same conditions, irradiated Xr-Q A2 films were stored and scanned measurement in order to obtain a more reliable result. The attenuation factors, evaluated by Xr-Q A2 radiochromic films, indicate that both composites are good candidates for use as patient radiation shielding in high dose medical procedures. (Author)

  11. In-situ synthesized (Al3Zr+Al2O3)p/A356 composites by direct melt reaction in Al-Zr-O system

    Institute of Scientific and Technical Information of China (English)

    赵玉涛; 李忠华; 程晓农; 戴起勋; 蔡兰

    2003-01-01

    A novel in-situ reaction system Al-Zr-O was developed. In situ Al3Zr and Al2O3 particulate reinforced A356 alloy matrix composites have been fabricated by direct melt reaction method. The results show that the maximum sizes of Al3Zr and Al2O3 particulates synthesized in the system ZrOCl2-A356 are 1 μm and 3 μm respectively, and they are well distributed in the matrix. The investigation shows that the Al3Zr crystal is in the shape of polyhedron and rectangle. There is a faceted growth phenomenon on Al3Zr crystal surface. It is firstly found that the Al3Zr crystal grows in the mechanism of twinning. The twinning plane is (1 1 4), and the twinning direction is [2 2 1]. The crystal morphology of in-situ α-Al2O3 particulate is rectangle or sphere. Furthermore, (Al3Zr+Al2O3)p/A356 composites have not only higher tensile strength at room temperature (376.2 MPa) but also higher yield strength (319.4 MPa) and higher tensile strength at elevated temperature (200 ℃) than those of the A356 alloy. The dry sliding wear test shows that the wear resistance of the (Al3Zr+Al2O3)p/A356 composites is greatly enhanced with increasing particulate volume fraction.

  12. Microwave dielectric properties of composites consisting of MgAl2O4 filler synthesized by molten-salt method and isotactic polypropylene polymer matrix

    Science.gov (United States)

    Takahashi, Susumu; Imai, Yusuke; Kan, Akinori; Hotta, Yuji; Ogawa, Hirotaka

    2015-10-01

    MgAl2O4 particles were synthesized through the solid-state reaction method (MAO-S) or molten-salt method (MAO-M). The crystallinity, particle size, and crystal structure of spinel-structured MAO-S and MAO-M particles were characterized and these particles used as dielectric fillers were filled into an isotactic polypropylene matrix, up to 30 vol % filler concentration. Significant differences in the degree of inversion (λ), which represents the cation distribution in tetrahedral and octahedral sites, were obtained for MAO-S and MAO-M by solid-state NMR measurements and the λ value of MAO-S fired for 10 h was 0.39, while that of MAO-M fired for 10 h was 0.64. The dielectric constant of MAO-S- or MAO-M-filled composites increased from 2.4 to 3.7 with increasing filler concentration and was consistent with the Bruggeman model. The dielectric loss and thermal conductivity of the composites were remarkably improved by the addition of the MAO-M filler, depending on the increase in the duration of firing, and were 1.74 × 10-4 and 0.62 W/(m·K), respectively. The coefficient of thermal expansion and the temperature coefficient of the dielectric constant of composites also depended on the filler concentration.

  13. Waveform synthesizer

    Science.gov (United States)

    Franks, Larry A.; Nelson, Melvin A.

    1981-01-01

    A method of producing optical and electrical pulses of desired shape. An optical pulse of arbitrary but defined shape illuminates one end of an array of optical fiber waveguides of differing lengths to time differentiate the input pulse. The optical outputs at the other end of the array are combined to form a synthesized pulse of desired shape.

  14. Hydrothermally Processed Oxide Nanostructures and Their Lithium–ion Storage Properties

    Directory of Open Access Journals (Sweden)

    Kim Yong-Jin

    2010-01-01

    Full Text Available Abstract Y- and Si-based oxide nanopowders were synthesized by a hydrothermal reaction of Y or Si powders with NaOH or LiOH aqueous solution. Nanoparticles with different morphology such as elongated nanospheres, flower-like nanoparticles and nanowires were produced by a control of processing parameters, in particular, the starting composition of solution. The preliminary result of electrochemical examination showed that the hydrothermally processed nanowires exhibit high initial capacities of Li-ion storage: 653 mAh/g for Y2O3 nanowires as anode materials and 186 mAh/g for Li2Si2O5 nanowires as cathode materials in a Li secondary cell. Compared to the powder with elongated sphere or flower-like shapes, the nanowires showed a higher Li-ion capacity and a better cycle property.

  15. Converting ultrasonic induction heating deposited monetite coating to Na-doped HA coating on H 2O 2-treated C/C composites by a two-step hydrothermal method

    Science.gov (United States)

    Xin-bo, Xiong; Jian-feng, Hung; Xie-rong, Zeng; Cen-cen, Chu

    2011-10-01

    a monetite coating on H 2O 2-treated C/C composites was prepared by ultrasonic induction heating (UIH) technology. Subsequently, this coating was subjected to an ammonia hydrothermal treatment to form a undoped hydroxyapatite (U-HA) coating. Finally, the as-prepared U-HA coating was placed in a NaOH solution and hydrothermally treated to produce the other hydroxyapatite (Na-HA) coating. The structure, morphology and chemical composition of the two HA coatings were characterized by XRD, FTIR, SEM and EDS, the adhesiveness and local mechanical properties, e.g. nanohardness and Young's modulus of the two HA coatings to C/C composites was evaluated by a scratch test and nanoindentation technique respectively. The results showed that the two HA coatings had the alike morphology and crystallization. But, compared with the U-HA coating, the Na-HA coating was doped with Na ions, and gave a Ca/P ratio close to a stoichiometric hydroxyapatite, and thus showed a higher nano-indentation value, Young's modulus, and larger bonding strength. These results verified the strengthened effect of Na ion in hydroxyapatite coating on carbon/carbon (C/C) composities.

  16. A novel three-dimensional sulfur/graphene/carbon nanotube composite prepared by a hydrothermal co-assembling route as binder-free cathode for lithium–sulfur batteries

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Guanghui; Wang, Gang [Northwest University, National Key Laboratory of Photoelectric Technology and Functional Materials (Culture Base), National Photoelectric Technology and Functional Materials & Application International Cooperation Base, Physics Department, Institute of Photonics & Photon-Technology (China); Wang, Hui, E-mail: huiwang@nwu.edu.cn [Northwest University, Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry & Materials Science (China); Bai, Jintao, E-mail: jintaobai@sina.cn, E-mail: baijt@nwu.edu.cn [Northwest University, National Key Laboratory of Photoelectric Technology and Functional Materials (Culture Base), National Photoelectric Technology and Functional Materials & Application International Cooperation Base, Physics Department, Institute of Photonics & Photon-Technology (China)

    2015-01-15

    A novel sulfur/graphene/carbon nanotube (S/GN/CNT) composite was successfully prepared by a facile hydrothermal co-assembling route. When used as cathode for lithium–sulfur battery, the S/GN/CNT composite can be pressed directly onto nickel foam without binder and conductive additive, thereby simplifying the manufacturing process. The resulting S/GN/CNT composite exhibited high and stable-specific discharge capacities of 670 mAh g{sup −1} after 80 cycles at 0.2 C and good rate capability. This enhanced electrochemical performance could be attributed to the combinative effects of GN and CNT, which not only function as a flexible conductive matrix, favoring the ion transport and electrolyte diffusion, but also for provide a porous three-dimensional architecture with open channels to effectively confine the soluble polysulfides.

  17. A novel three-dimensional sulfur/graphene/carbon nanotube composite prepared by a hydrothermal co-assembling route as binder-free cathode for lithium-sulfur batteries

    Science.gov (United States)

    Yuan, Guanghui; Wang, Gang; Wang, Hui; Bai, Jintao

    2015-01-01

    A novel sulfur/graphene/carbon nanotube (S/GN/CNT) composite was successfully prepared by a facile hydrothermal co-assembling route. When used as cathode for lithium-sulfur battery, the S/GN/CNT composite can be pressed directly onto nickel foam without binder and conductive additive, thereby simplifying the manufacturing process. The resulting S/GN/CNT composite exhibited high and stable-specific discharge capacities of 670 mAh g-1 after 80 cycles at 0.2 C and good rate capability. This enhanced electrochemical performance could be attributed to the combinative effects of GN and CNT, which not only function as a flexible conductive matrix, favoring the ion transport and electrolyte diffusion, but also for provide a porous three-dimensional architecture with open channels to effectively confine the soluble polysulfides.

  18. Coupling hydrothermal liquefaction and anaerobic digestion for energy valorization from model biomass feedstocks.

    Science.gov (United States)

    Posmanik, Roy; Labatut, Rodrigo A; Kim, Andrew H; Usack, Joseph G; Tester, Jefferson W; Angenent, Largus T

    2017-06-01

    Hydrothermal liquefaction converts food waste into oil and a carbon-rich hydrothermal aqueous phase. The hydrothermal aqueous phase may be converted to biomethane via anaerobic digestion. Here, the feasibility of coupling hydrothermal liquefaction and anaerobic digestion for the conversion of food waste into energy products was examined. A mixture of polysaccharides, proteins, and lipids, representing food waste, underwent hydrothermal processing at temperatures ranging from 200 to 350°C. The anaerobic biodegradability of the hydrothermal aqueous phase was examined through conducting biochemical methane potential assays. The results demonstrate that the anaerobic biodegradability of the hydrothermal aqueous phase was lower when the temperature of hydrothermal processing increased. The chemical composition of the hydrothermal aqueous phase affected the anaerobic biodegradability. However, no inhibition of biodegradation was observed for most samples. Combining hydrothermal and anaerobic digestion may, therefore, yield a higher energetic return by converting the feedstock into oil and biomethane. Copyright © 2017 Elsevier Ltd. All rights reserved.

  19. Hydrogen storage kinetics of nanocrystalline and amorphous NdMg{sub 12}-type alloy-Ni composites synthesized by mechanical milling

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yanghuan; Cui, Songsong; Cai, Ying [Inner Mongolia University of Science and Technology, Baotou (China). Lab. of Integrated Exploitation of Baiyun Obo Multi-Metal Resources; Song, Xiping [Univ. of Science and Technology, Beijing (China). State Key Lab. for Advanced Metals and Materials; Zhang, Peilong; Zhu, Yongguo [Whole Win (Beijing) Materials Sci. and Tech. Co., Ltd., Beijing (China)

    2016-07-15

    Nanocrystalline and amorphous NdMg{sub 11}Ni + x wt.% Ni (x = 100, 200) composites were synthesized by mechanical milling, and their gaseous and electrochemical hydrogen storage kinetic performances were systematically investigated. Hydrogen absorption and desorption properties were investigated by means of a Sievert apparatus and a differential scanning calorimeter connected with an H{sub 2} detector. Electrochemical hydrogen storage kinetics of the as-milled alloys were tested by an automatic galvanostatic system. Results show that increasing Ni content significantly improves gaseous and electrochemical hydrogen storage kinetics. The improved gaseous hydrogen storage kinetics of the alloys are ascribed to the decrease in hydrogen desorption activation energy caused by increasing Ni content and milling time.

  20. Nanoscale-phase-separated Pd-Rh boxes synthesized via metal migration: an archetype for studying lattice strain and composition effects in electrocatalysis.

    Science.gov (United States)

    Sneed, Brian T; Brodsky, Casey N; Kuo, Chun-Hong; Lamontagne, Leo K; Jiang, Ying; Wang, Yong; Tao, Franklin Feng; Huang, Weixin; Tsung, Chia-Kuang

    2013-10-02

    Developing syntheses of more sophisticated nanostructures comprising late transition metals broadens the tools to rationally design suitable heterogeneous catalysts for chemical transformations. Herein, we report a synthesis of Pd-Rh nanoboxes by controlling the migration of metals in a core-shell nanoparticle. The Pd-Rh nanobox structure is a grid-like arrangement of two distinct metal phases, and the surfaces of these boxes are {100} dominant Pd and Rh. The catalytic behaviors of the particles were examined in electrochemistry to investigate strain effects arising from this structure. It was found that the trends in activity of model fuel cell reactions cannot be explained solely by the surface composition. The lattice strain emerging from the nanoscale separation of metal phases at the surface also plays an important role.

  1. Effect of electrical parameters on morphology, chemical composition, and photoactivity of the nano-porous titania layers synthesized by pulse-microarc oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Bayati, M.R., E-mail: bayati@iust.ac.i [School of Metallurgy and Materials Engineering, Iran University of Science and Technology, P.O. Box: 16845-161, Tehran (Iran, Islamic Republic of); Center of Excellence for Advanced Materials, Iran University of Science and Technology, P.O. Box: 16845-195, Tehran (Iran, Islamic Republic of); Moshfegh, A.Z. [Department of Physics, Sharif University of Technology, P.O. Box: 11155-9161, Tehran (Iran, Islamic Republic of); Institute for Nanoscience and Nanotechnology, Sharif University of Technology, P.O. Box 14588-89694, Tehran (Iran, Islamic Republic of); Golestani-Fard, F. [School of Metallurgy and Materials Engineering, Iran University of Science and Technology, P.O. Box: 16845-161, Tehran (Iran, Islamic Republic of); Center of Excellence for Advanced Materials, Iran University of Science and Technology, P.O. Box: 16845-195, Tehran (Iran, Islamic Republic of)

    2010-03-01

    TiO{sub 2} layers were grown via pulse type microarc oxidation process under different applied voltages, frequencies, and duty cycles. Surface chemical composition and phase structure of the synthesized layers were studied utilizing X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). Furthermore, scanning electron microscope (SEM) and atomic force microscope (AFM) were employed to investigate surface morphology and topography of the layers. It was revealed that the layers had a porous structure with both anatase and rutile phases. The anatase relative content in the layers increased with the applied frequency; meanwhile, it decreased with duty cycle at low applied voltages, but increased with duty cycle at high applied voltages. The topographical evaluations showed that the surface of the layers is rough with an average roughness of about 1.8-9.9 nm. It was also found that the pore size decreased with the current frequency and increased with duty cycle at a fixed applied voltage. Photocatalytic performance of the layers was also examined by measuring the decomposition rate of methylene blue solution under ultraviolet irradiation of the surface. It was also found that about 94% of methylene blue solution was decomposed on the synthesized catalysts after 160 min UV irradiation of the surface.

  2. Silylated pillared clay (SPILC): A novel bentonite-based inorgano-organo composite sorbent synthesized by integration of pillaring and silylation.

    Science.gov (United States)

    Zhu, Lizhong; Tian, Senlin; Zhu, Jianxi; Shi, Yao

    2007-11-01

    This research examines the feasibility of synthesizing inorgano-organo composites based on bentonite-silylated pillared interlayered clays (SPILCs) by pre-pillaring of bentonite with the Keggin ion (hydroxyaluminum polycation) and then silylating with alkylchlorosilanes. The results of organic carbon content analysis, FTIR, XRD, and DTA/TG indicated that the silyl group can be successfully grafted to the inner surface of pillared interlayered clays (PILCs) through reaction with the OH groups of the pillars and the d-spacing of synthesized PILCs and SPILCs were almost the same. SPILCs have both the higher organic carbon content relative to original bentonite and PILCs and the better surface and pore properties relative to surfactants-modified organobentonites. A comparison of the modifier demand of SPILCs and CTMAB-bentonites indicated that the silylation of PILCs was a modifier-economized process for organically modification of bentonite. The heat-resistant temperature of SPILCs, 508 degrees C for OTS-Al-PILC and 214 degrees C for TMCS-Al-PILC, are more excellent organobentonites. Unlike the partition-predominated sorption mechanisms of organobentonites, both adsorption and partition are important components of sorption mechanism of SPILCs. The VOC sorption capacity of SPILCs is approximately same with that of organobentonites and the hydrophobicity of SPILCs is superior to that of PILCs.

  3. Vanadium Pentoxide-Based Composite Synthesized Using Microwave Water Plasma for Cathode Material in Rechargeable Magnesium Batteries

    Directory of Open Access Journals (Sweden)

    Tatsuhiko Yajima

    2013-10-01

    Full Text Available Multivalent cation rechargeable batteries are expected to perform well as high-capacity storage devices. Rechargeable magnesium batteries have an advantage in terms of resource utilization and safety. Here, we report on sulfur-doped vanadium pentoxide (S-V2O5 as a potential material for the cathodes of such a battery; S-V2O5 showed a specific capacity of 300 mAh·g−1. S-V2O5 was prepared by a method using a low-temperature plasma generated by carbon felt and a 2.45 GHz microwave generator. This study investigates the ability of S-V2O5 to achieve high capacity when added to metal oxide. The highest recorded capacity (420 mAh·g−1 was reached with MnO2 added to composite SMn-V2O5, which has a higher proportion of included sulfur than found in S-V2O5. Results from transmission electron microscopy, energy-dispersive X-ray spectroscopy, Micro-Raman spectroscopy, and X-ray photoelectron spectroscopy show that the bulk of the SMn-V2O5 was the orthorhombic V2O5 structure; the surface was a xerogel-like V2O5 and a solid solution of MnO2 and sulfur.

  4. Chemical composition and structural phase changes of Pd sample and properties of novel synthesized structure at dense deuterium gas under irradiation by γ-quanta

    Science.gov (United States)

    Didyk, A. Yu.; Wiśniewski, R.

    2012-12-01

    Studies have been carried out into the element composition of Pd and brass with associated materials and synthesized novel structure, placed in dense deuterium gas in a deuterium high-pressure chamber (DHPC) under the pressure 3 kbar and irradiated with γ-quanta of energy up to 8.8 MeV. Using the methods of scanning electron microscopy, microelement chemical analysis and X-ray diffraction, it was determined that in the absence in the chamber volume and walls of all HPC-forming materials the synthesized structure is largely composed of alumosilicates and Al and Si oxides with high content of Ti compounds as rutile TiO2. Pd1.5D2. Considerable anomalies in the chemical composition were found both in the surface and at large depth in a Pd specimen. The entire Pd surface turned into a structure comprised of Pd clusters, Cu and Zn compounds, with a notable content of Mg, Al, S, Si, K, Ca, Ti and Fe compounds. Results of evaluative calculations, including computation of the Q-value, are presented for nuclear reactions produced in a saturated with deuterium Pd specimen and dense deuterium gas under the action of γ-quanta, neutrons and protons of energies up to E n + E p ≈ E γ - E D MeV generated by deuteron fission. The obtained results can be explained by "collective effects" as chain reactions caused by deuteron fission induced by protons ( E p > 3.39 MeV) and neutrons ( E n > 2.25 MeV), as well as by thermonuclear synthesis of deuterium atoms elastically scattered by protons of energies up to E P < E γ - E D MeV.

  5. Synthesized TiO2/ZSM-5 composites used for the photocatalytic degradation of azo dye: Intermediates, reaction pathway, mechanism and bio-toxicity

    Science.gov (United States)

    Zhou, Kefu; Hu, Xin-Yan; Chen, Bor-Yann; Hsueh, Chung-Chuan; Zhang, Qian; Wang, Jiajie; Lin, Yu-Jung; Chang, Chang-Tang

    2016-10-01

    In this study, a one-step solid dispersion method was used to synthesize titanium dioxide (TiO2)/Zeolite Socony Mobil-5 (ZSM-5) composites with substantially reduced time and energy consumption. A degradation efficiency of more than 95% was achieved within 10 min using 50% PTZ (synthesized TiO2/ZSM-5 composites with TiO2 contents of 50 wt% loaded on ZSM-5) at pH 7 and 25 °C. The possible degradation pathway of azo-dye Reactive Black 5 (RB5) was investigated using gas chromatography-mass spectrometry and ion chromatography (IC). The bonds between the N atoms and naphthalene groups are likely attacked first and cleaved by hydroxyl radicals, ultimately resulting in the decolorization and mineralization of the azo dye. A comparative assessment of the characteristics of abiotic and biotic dye decolorization was completed. In addition, the toxicity effects of the degradation intermediates of azo-dye RB5 on cellular respiratory activity were analyzed. The bio-toxicity results showed that the decay rate constants of CO2 production from the azo-dye RB5 samples at different degradation times increased initially and subsequently decreased, indicating that intermediates of higher toxicity could adhere to the catalyst surface and gradually destroyed by further photocatalytic oxidation. Additionally, EDTA (hole scavengers) and t-BuOH (radical scavengers) were used to detect the main active oxidative species in the system. The results showed that the hydroxyl radicals are the main oxidation species in the photocatalytic process.

  6. Dynamics of the Yellowstone hydrothermal system

    Science.gov (United States)

    Hurwitz, Shaul; Lowenstern, Jacob B.

    2014-01-01

    The Yellowstone Plateau Volcanic Field is characterized by extensive seismicity, episodes of uplift and subsidence, and a hydrothermal system that comprises more than 10,000 thermal features, including geysers, fumaroles, mud pots, thermal springs, and hydrothermal explosion craters. The diverse chemical and isotopic compositions of waters and gases derive from mantle, crustal, and meteoric sources and extensive water-gas-rock interaction at variable pressures and temperatures. The thermal features are host to all domains of life that utilize diverse inorganic sources of energy for metabolism. The unique and exceptional features of the hydrothermal system have attracted numerous researchers to Yellowstone beginning with the Washburn and Hayden expeditions in the 1870s. Since a seminal review published a quarter of a century ago, research in many fields has greatly advanced our understanding of the many coupled processes operating in and on the hydrothermal system. Specific advances include more refined geophysical images of the magmatic system, better constraints on the time scale of magmatic processes, characterization of fluid sources and water-rock interactions, quantitative estimates of heat and magmatic volatile fluxes, discovering and quantifying the role of thermophile microorganisms in the geochemical cycle, defining the chronology of hydrothermal explosions and their relation to glacial cycles, defining possible links between hydrothermal activity, deformation, and seismicity; quantifying geyser dynamics; and the discovery of extensive hydrothermal activity in Yellowstone Lake. Discussion of these many advances forms the basis of this review.

  7. The photocatalytic properties of hollow (GaN)1-x(ZnO)x composite nanofibers synthesized by electrospinning

    Science.gov (United States)

    Wang, Ding; Zhang, Minglu; Zhuang, Huaijuan; Chen, Xu; Wang, Xianying; Zheng, Xuejun; Yang, Junhe

    2017-02-01

    (GaN)1-x(ZnO)x composite nanofibers with hollow structure were prepared by initial electrospinning, and the subsequent calcination and nitridation. The structure and morphology characteristics of samples were investigated by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDS) and transmission electron microscopy (TEM). The characterization results showed the phase transition from ZnGa2O4 to (GaN)1-x(ZnO)x solid-solution under ammonia atmosphere. The preparation conditions were explored and the optimum nitridation temperature and holding time are 750 °C and 2 h, respectively. The photocatalytic properties of (GaN)1-x(ZnO)x with different Ga:Zn atomic ratios were investigated by degrading Rhodamine B under the visible light irradiation. The photocatalytic activity sequence is (GaN)1-x(ZnO)x (Ga:Zn = 1:2) > (GaN)1-x(ZnO)x (Ga:Zn = 1:3) > ZnO nanofibers > (GaN)1-x(ZnO)x (Ga:Zn = 1:4) > (GaN)1-x(ZnO)x (Ga:Zn = 1:1). The photocatalytic mechanism of the (GaN)1-x(ZnO)x hollow nanofibers was further studied by UV-vis diffuse reflectance spectra. The excellent photocatalytic performance of (GaN)1-x(ZnO)x hollow nanofibers was attributed to the narrow band gap and high surface area of porous nanofibers with hollow structure.

  8. STRUCTURE CONTROL IN HYDROXYAPATITE SYNTHESIS BY HYDROTHERMAL REACTION AND ORGANIC MODULATORS

    Institute of Scientific and Technical Information of China (English)

    Huigang Zhang; Qingshan Zhu

    2005-01-01

    Properties of materials are determined not only by their composition, but also by their structure. It is,therefore, of great significance to develop the ability of tailoring the structure of materials according to the requirements of intended applications. In this work a novel glutamic acid-assisted hydrothermal process was developed to synthesize apatite crystals with controllable morphologies. Varied morphologies from whisk broom, fibers, mushroom, prickly spheres, to dandelion were produced through modulating both the formation of a transitory phase and its transformation into the final phase.

  9. Boehmite nanostructures preparation by hydrothermal method from anodic aluminium oxide membrane.

    Science.gov (United States)

    Yang, X; Wang, J Y; Pan, H Y

    2009-02-01

    Boehmite nanostructures were successfully synthesized from porous anodic aluminium oxide (AAO) membrane by a simple and efficient hydro-thermal method. The experiment used high purity alumina as raw material, and the whole reaction process avoided superfluous impurities to be introduced. Thus, the purity of Boehmite products was ensured. The examinations of the morphology and structure were carried out by atomic force microscope (AFM), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Composition of the specimens was analyzed using energy dispersive X-ray spectroscope (EDX) and X-ray diffraction (XRD). Based on these observations the growth process was analyzed.

  10. Simulation, design and proof-of-concept of a two-stage continuous hydrothermal flow synthesis reactor for synthesis of functionalized nano-sized inorganic composite materials

    DEFF Research Database (Denmark)

    Zielke, Philipp; Xu, Yu; Simonsen, Søren Bredmose

    2016-01-01

    Computational fluid dynamics simulations were employed to evaluate several mixer geometries for a novel two-stage continuous hydrothermal flow synthesis reactor. The addition of a second stage holds the promise of allowing the synthesis of functionalized nano-materials as for example core...

  11. Performance of LiFePO4/C synthesized by hydrothermal with different reaction system%不同反应体系水热合成的LiFePO4/C的性能

    Institute of Scientific and Technical Information of China (English)

    娄永兵; 张静静; 朱林

    2013-01-01

    Cathode material carbon coated lithium iron phosphate(LiFePO4/C) was prepared by hydrothermal method with surfactant.The morphology,structure and electrochemical performance of the products were characterized by Fourier transform infrared spectroscopy (FT-IR),XRD,thermogravimetric (TG),SEM,galvanostatic charge-discharge and electrochemical impedance spectroscopy(EIS) tests.LiFePO4/C samples were small particles with pure phase and regular shape.LiFePO4/C particles showed different morphology and grain size when the surfactant changed.LiFePO4/C samples prepared with PVP and PEG-400 could deliver the initial discharge specific capacity of 154.1 mAh/g and 145.6 mAh/g at 0.1 C when cycled in 2.0 ~ 4.2 V.When cycle 24 times,the capacity retention at 0.5 C was 71% and 75%,respectively,the capacity retention at 1.0 C was 65% and 62%,respectively.%添加表面活性剂,采用水热法合成正极材料碳包覆的磷酸铁锂(LiFePO4/C),用傅立叶红外光谱(FT-IR)、XRD、热重(rG)、SEM、恒流充放电和电化学阻抗谱等进行分析.制得的LiFePO4/C材料纯度高、粒径小且形貌较规则.使用不同表面活性剂制备的LiFePO4/C颗粒具有不同的形貌和粒径.使用聚乙烯吡咯烷酮(PVP)高分子和聚乙二醇(PEG-400)低分子制备的LiFePO4/C材料,在2.0~4.2 V充放电,0.1C首次放电比容量分别为154.1 mAh/g和145.6 mAh/g;循环24次,0.5C时的容量保持率分别为71%和75%,1.0C时的容量保持率分别为65%和62%.

  12. Silver Doped TiO2 Nanostructure Composite Photocatalyst Film Synthesized by Sol-Gel Spin and Dip Coating Technique on Glass

    Directory of Open Access Journals (Sweden)

    Mojtaba Nasr-Esfahani

    2008-01-01

    Full Text Available New composite films (P25SGF-MC-Ag, MPC500SGF-MC-Ag, and ANPSGF-MC-Ag have been synthesized by a modified sol-gel method using different particle sizes of TiO2 powder and silver addition. Nanostructure TiO2/Ag composite thin films were prepared by a sol-gel spin and dip coating technique. while, by introducing methyl cellulose (MC porous, TiO2/Ag films were obtained after calcining at a temperature of 500°C. The as-prepared TiO2 and TiO2/Ag films were characterized by X-ray diffractometry, and scanning electron microscopy to reveal the structural and morphological differences. In addition, the photocatalytic properties of these films were investigated by degrading methyl orange (MO under UV irradiation. After 500°C calcination, the microstructure of MC-TiO2 film without Ag addition exhibited a microstructure, while significant sintering effect was noticed with Ag additions and the films exhibited a porous microstructure. Nanostructure anatase-phase TiO2 can be observed with respect to the sharpening of XRD diffraction peaks. The photodegradation of porous TiO2 deposited with 5×10−4 mol Ag exhibited the best photocatalytic efficiency, where 69% methyl orange can be decomposed after UV exposure for 1 hour.

  13. Mesoporous composite nickel cobalt oxide/graphene oxide synthesized via a template-assistant co-precipitation route as electrode material for supercapacitors

    Science.gov (United States)

    Xu, Yanjie; Wang, Lincai; Cao, Peiqi; Cai, Chuanlin; Fu, Yanbao; Ma, Xiaohua

    2016-02-01

    A simple co-precipitation method utilizing SDS (sodium dodecyl sulfate) as template and ammonia as precipitant is successfully employed to synthesize nickel cobalt oxide/graphene oxide (NiCo2O4/GO) composite. The as-prepared composite (NCG-10) exhibits a high capacitance of 1211.25 F g-1, 687 F g-1 at the current density of 1 A g-1, 10 A g-1 and good cycling ability which renders NCG-10 as promising electrode material for supercapacitors. An asymmetric supercapacitor (ASC) (full button cell) has been constructed with NCG-10 as positive electrode and lab-made reduced graphene oxide (rGO) as negative electrode. The fabricated NCG-10//rGO with an extended stable operational voltage of 1.6 V can deliver a high specific capacitance of 144.45 F g-1 at a current density of 1 A g-1. The as-prepared NCG-10//rGO demonstrates remarkable energy density (51.36 W h kg-1 at 1 A g-1), high power density (50 kW kg-1 at 20 A g-1). The retention of capacitance is 88.6% at the current density of 8 A g-1 after 2000 cycles. The enhanced capacitive performance can be attributed to the improved specific surface area and 3D open area of NCG-10 generated by the pores and channels with the substantial function of SDS.

  14. Microstructure and properties of hot extruded Cu–1 wt% Al{sub 2}O{sub 3} nano-composites synthesized by various techniques

    Energy Technology Data Exchange (ETDEWEB)

    Chandrasekhar, S.B., E-mail: chandru@arci.res.in [International Advanced Research Centre for Powder Metallurgy and New Materials (ARCI), Balapur P.O, Hyderabad 500005 (India); Sudhakara Sarma, S.; Ramakrishna, M.; Suresh Babu, P.; Rao, Tata N. [International Advanced Research Centre for Powder Metallurgy and New Materials (ARCI), Balapur P.O, Hyderabad 500005 (India); Kashyap, B.P. [Department of Metallurgical Engineering and Materials Science, Indian Institute of Technology Bombay, Mumbai 400076 (India)

    2014-01-03

    Cu–1 wt% Al{sub 2}O{sub 3} nano-composites were prepared by three different methods, namely mechanical alloying, combustion synthesis and electrical explosion of wire, in order to investigate the effect of power processing technique on microstructure and ambient properties. The powders produced by these techniques were hydrogen reduced at 500 °C and subsequently vacuum encapsulated in copper container followed by consolidation using hot extrusion at 800 °C and 600 MPa to nearly full density. As-synthesized composite powders as well as the extruded samples were characterized by scanning electron microscope, X-ray diffraction, transmission electron microscope, thermal conductivity and electrical conductivity. Microhardness and room temperature deformation behavior in compression at a strain rate of 10{sup −4} s{sup −1} were measured. The mechanically milled powders, upon consolidation, exhibited a finer grain size of 146 nm and a hardness of 164 HV1.0 compared to that obtained by two other techniques, which ranged between 179–390 nm and 135–156 HV1.0, respectively. The physical and mechanical properties were found to vary with grain size according to the Hall-Petch type relationship, irrespective of the processing technique employed for getting these grain sizes.

  15. 水热法制备ZnO/TiO2复合粉体及其电池性能%Preparation of ZnO/TiO2 Composite Nanopowders by Hydrothermal Method and its Photovoltaic Properties

    Institute of Scientific and Technical Information of China (English)

    王艳香; 高智丹; 赵学国; 范学运; 杨志胜; 黄丽群; 李家科; 孙健

    2016-01-01

    采用水热法制备TiO2和ZnO/ TiO2复合粉体,将不同Zn2+/Ti4+摩尔比制备的ZnO/TiO2复合粉制备浆料,采用刮涂法在掺氟的SnO2透明导电玻璃(FTO)上制备ZnO/TiO2复合光阳极薄膜,与Pt对电极和电解质组装成染料敏化太阳能电池。采用X射线衍射仪(XRD)和扫描电镜(SEM)对所制备样品的物相组成和形貌进行表征,通过光电性能和电化学阻抗谱测试,研究Zn2+/Ti4+摩尔比对ZnO/TiO2复合光阳极电池性能的影响。结果表明:基于纯TiO2的DSSC的短路电流密度Jsc为1.77 mA/cm2,光电装换效率为0.90%;当Zn2+/Ti4+摩尔比为1:1时,ZnO/TiO2粉体制备的DSSC短路电流密度Jsc和光电转换效率达到最大,分别为2.88 mA/cm2和1.26%,比纯TiO2的转换效率提高了40%。%TiO2 and ZnO/TiO2 nanopowders were prepared by hydrothermal method. The ZnO/TiO2 composite photoanodes with different Zn2+/Ti4+ molar ratios were prepared on the transparent conductive fluorine-doped SnO2(FTO) substrates by doctor-blade method. These photoanodes were assembled into dye-sensitized solar cells (DSSCs) together with Pt-counter electrode and liquid electrolyte. XRD and SEM were used to characterize the phase composition and morphology of the synthesized samples. Results showed that the Jsc and Eff of the DSSC based on the pure TiO2 photoanode were 1.77 mA/cm2 and 0.9 %, respectively. The Jsc and Eff of the DSSC fabricated from ZnO/TiO2 powder with the Zn2+/Ti4+ ratio of 1:1 were optimum, which were 2.88 mA/cm2 and 1.26%. The Eff was 40 % higher than that of pure TiO2 based DSSC.

  16. Synthesis on the durability of composite fiberglass/epoxy resin structures; Synthese sur la durabilite des structures composites en fibres de verre/resine epoxide

    Energy Technology Data Exchange (ETDEWEB)

    Thevenin, P. [Electricite de France (EDF), Direction des Etudes et Recherches, 92 - Clamart (France)

    1997-12-31

    The purpose of this paper is to collect together in a systematic way information and results relating to the durability of composite fiberglass/ epoxy resin structures. First it is a matter of assessing the average level of understanding the long term behaviour of these structures which change under the combined effects of varied mechanical loading and stresses of a physico-chemical type linked to the environment. Looking at phenomena encountered and facts from current analyses, it will then be advisable to specify a methodology which can be applied to industrial piping used in PWR cooling systems for transporting raw water under pressure. In fact assessment of their service life is at present based on long and costly testing (ASTM D 2992 B standard), the appearance of which is inherited from metal piping testing.. Therefore it appears essential to study substitution test procedures, more composite specific and at the same time which can be conducted in reasonable time. For this purpose, by coherently accelerating and combining them in order not to underestimate their effects, ageing tests shall reproduce mechanisms representative of operating conditions. (author). 113 refs.

  17. Structural, chemical and optical properties of the polyethylene–copper sulfide composite thin films synthesized using polythionic acid as sulfur source

    Energy Technology Data Exchange (ETDEWEB)

    Ancutiene, Ingrida [Department of Physical and Inorganic Chemistry, Kaunas University of Technology, Radvilenu st. 19, LT-50254 Kaunas (Lithuania); Navea, Juan G. [Chemistry Department, Skidmore College, 815N. Broadway, Saratoga Springs, NY 12866 (United States); Baltrusaitis, Jonas, E-mail: job314@lehigh.edu [Department of Chemical and Biomolecular Engineering, Lehigh University, B336 Iacocca Hall, 111 Research Drive, Bethlehem, PA 18015 (United States)

    2015-08-30

    Graphical abstract: Several crystalline copper sulfide phases (spionkopite, anilite, digenite, djurleite, chalcocite) were obtained in as synthesized samples (PE-Cu{sub x}S) and elucidated using XRD. Thickness of the films obtained ranged from several microns to ∼18 μm and depended on the Cu(II/I) exposure time. Bandgap of the materials obtained was measured and ranged from 1.88 to 1.17 eV. Importantly, heating samples, many copper sulfide crystalline phase containing films at 100 °C in inert atmosphere invariably resulted in a single copper sulfide, anilite (Cu{sub 1.75}S), phase. - Highlights: • We investigated deposition of a single phase copper sulfide on polyethylene. • A single sulfur precursor – H{sub 2}S{sub 33}O{sub 6} – was used. • Increasing exposure time to Cu(II/I) yielded Cu{sub x}S with higher x values. • Heating at 100 °C in N{sub 2} resulted in a single anilite (Cu{sub 1.75}S) phase. • Cu(I) and Cu(II) compounds were detected using XPS. - Abstract: Synthesis and properties of thin copper sulfide films deposited on polyethylene were explored for the development of low cost hybrid organic–inorganic photovoltaic materials. Polyethylene was used as a model organic host material for thin copper sulfide film formation. Adsorption–diffusion method was used which utilized consecutive exposure of polyethylene to polythionic acid followed by aqueous Cu(II/I) solution. Several crystalline copper sulfide phases were obtained in synthesized samples and elucidated using X-ray diffraction. Surface chemical composition determined using X-ray photoelectron spectroscopy showed the presence of copper sulfides in combination with copper hydroxide. Thickness of the composite material films ranged from several microns to ∼18 μm and depended on the Cu(II/I) exposure time. Bandgap of the materials obtained was measured and ranged from 1.88 to 1.17 eV. Importantly, heating these complex copper sulfide crystalline phase containing films at 100

  18. Hydrothermal Synthesis and Photocatalytic Activity of Partially Reduced Graphene Oxide/TiO2 Composite%部分还原氧化石墨烯/二氧化钛复合材料的水热合成及其光催化活性

    Institute of Scientific and Technical Information of China (English)

    龙梅; 丛野; 李轩科; 崔正威; 董志军; 袁观明

    2013-01-01

      采用水热法以Hummers氧化法制备的氧化石墨和钛酸四丁酯为原料制备了部分还原的氧化石墨烯/二氧化钛(RGO/TiO2)复合光催化剂,并研究了该复合材料在可见光以及紫外光下对亚甲基蓝的光催化降解活性。结果表明,通过改变反应温度和氧化石墨加入量可以调控TiO2的晶相组成及其在复合材料中的分散性;在水热反应过程中氧化石墨烯发生了部分还原;所制备的 RGO/TiO2复合材料的可见光和紫外光催化活性均高于纯TiO2;部分还原的氧化石墨烯在复合材料中担当载体和电子受体,同时可以使TiO2的初始吸收边向可见光区域红移,增强了TiO2在可见光区域的吸收,能有效提高对目标污染物的吸附性和光催化降解活性。%Partial y reduced graphene oxide/titanium dioxide (RGO/TiO2) composite was synthesized using tetrabutyl titanate and graphite oxide by a hydrothermal method. Photocatalytic activity of the material was evaluated by the degradation of methylene blue solution under visible light and UV light. The results suggest that the crystal phase and dispersion of titanium oxide in the composite can be control ed by varying the reaction temperature and amount of graphite oxide. Graphene oxide was partial y reduced in the hydrothermal reaction process. Photocatalytic activities of partial y reduced graphene oxide/titanium dioxide composites under both visible and UV light irradiation were higher than those of pure TiO2. Partial y reduced graphene oxide may act as a support and electron acceptor, and can also extend and enhance the band edge absorption of TiO2 into the visible light region, hence effectively enhancing the adsorbability and photocatalytic activity of TiO2.

  19. Effects of ultrasonic treatment on zeolite synthesized from coal fly ash.

    Science.gov (United States)

    Belviso, Claudia; Cavalcante, Francesco; Lettino, Antonio; Fiore, Saverio

    2011-03-01

    The synthesis of zeolites from three samples of fly ash was carried out through a low-temperature (25-60°C) hydrothermal process with a NaOH pre-fusion treatment preceded by sonication. The results were compared with those of conventional hydrothermal syntheses. XRD and SEM investigations demonstrate that the application of ultrasonic treatment facilitates the formation of zeolites at a lower-temperature (25°C) than syntheses not preceded by sonication. No significant difference in type, temperature of crystallization, or amount of zeolites synthesized was noted between the three different samples of fly ash, implying that the chemical composition of fly ash had little influence on the zeolite product within the compositional range of these fly ash precursors. Although there appears to be a correlation between the SiO(2)/Al(2)O(3) ratio of the fly ash and the temperature of zeolite formation by conventional synthesis, no correlation was apparent when ultrasonic pre-treatment was used at low-temperatures.

  20. Review of Development of the Repair for Helicopter Composite Materials and Effects of Hydro-Thermal Environment%直升机复合材料修理及湿热环境影响研究综述

    Institute of Scientific and Technical Information of China (English)

    李俊婷; 马宝亮

    2016-01-01

    随着纤维增强树脂基复合材料在直升机结构上应用的不断增加,复合材料修理技术已变得越来越重要。而且,直升机(尤其是海上飞行的直升机)的飞行环境特别复杂,环境因素特别是湿热环境会使复合材料的一些性能降低。综述了复合材料的修理技术,包括预浸料和湿法铺层修理及真空辅助树脂转移模塑成形( VARTM)补片修理;分析了湿热环境对复合材料修理的影响。%With the increasing application of fiber reinforced resin composite materials in helicopter structures, repair technology of composite materials has becoming more and more important. Moreo-ver, the fly environments of helicopters are very complex, in particular the helicopter flying over the sea. Environment, especial hydro-thermal environment, will make some properties of the compos-ite material degrade. This paper reviewed the repair technology, including prepreg, wet layup and VARTM( Vacuum Assisted ResinTransfer Molding) repair;effects of hydro-thermal environment on the repair, the aim of which was to provide a reference for the development of the repair technology for helicopter composite materials.

  1. Hydrothermally reduced graphene oxide as a supercapacitor

    Science.gov (United States)

    Johra, Fatima Tuz; Jung, Woo-Gwang

    2015-12-01

    The supercapacitance behavior of hydrothermally reduced graphene oxide (RGO) was investigated for the first time. The capacitive behavior of RGO was characterized by using cyclic voltammetry and galvanostatic charge-discharge methods. The specific capacitance of hydrothermally reduced RGO at 1 A/g was 367 F/g in 1 M H2SO4 electrolyte, which was higher than that of RGO synthesized via the hydrazine reduction method. The RGO-modified glassy carbon electrode showed excellent stability. After 1000 cycles, the supercapacitance was 107.7% of that achieved in the 1st cycle, which suggests that RGO has excellent electrochemical stability as a supercapacitor electrode material. The energy density of hydrothermal RGO reached 44.4 W h/kg at a power density of 40 kW/kg.

  2. Hydrothermal organic synthesis experiments

    Science.gov (United States)

    Shock, Everett L.

    1992-01-01

    Ways in which heat is useful in organic synthesis experiments are described, and experiments on the hydrothermal destruction and synthesis of organic compounds are discussed. It is pointed out that, if heat can overcome kinetic barriers to the formation of metastable states from reduced or oxidized starting materials, abiotic synthesis under hydrothermal conditions is a distinct possibility. However, carefully controlled experiments which replicate the descriptive variables of natural hydrothermal systems have not yet been conducted with the aim of testing the hypothesis of hydrothermal organic systems.

  3. Dielectric and piezoelectric properties of lead-free Ba{sub 0.85}Ca{sub 0.15}Ti{sub 0.9−x}Zr{sub 0.1}Cu{sub x}O{sub 3} ceramics synthesized by a hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Hunpratub, Sitchai [Material Science and Nanotechnology Programs, Faculty of Science, Khon Kaen University, Khon Kaen 40002 (Thailand); Phokha, Sumalin [Department of Physics, Faculty of Science, Udon Thani Rajabhat University, Udon Thani 41000 (Thailand); Maensiri, Santi [School of Physics, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima 30000 (Thailand); Chindaprasirt, Prinya, E-mail: prinya@kku.ac.th [Sustainable Infrastructure Research and Development Center, Department of Civil Engineering, Faculty of Engineering, Khon Kaen University, Khon Kaen 40002 (Thailand)

    2016-04-30

    Graphical abstract: Ba{sub 0.85}Ca{sub 0.15}Ti{sub 0.9−x}Zr{sub 0.1}Cu{sub x}O{sub 3} (x = 0.2, 0.4, 0.6, 0.8 and 1%) ceramics are prepared from nanopowders synthesized using a hydrothermal method at low sintering temperature of 1300 °C for 3 h. The samples are dense microstructures investigated by scanning electron microscopy (SEM). The dielectric constants, ferroelectric hysteresis loops of Ba{sub 0.85}Ca{sub 0.15}Ti{sub 0.9−x}Zr{sub 0.1}Cu{sub x}O{sub 3} ceramics are well character. - Highlights: • Ba{sub 0.85}Ca{sub 0.15}Ti{sub 0.9−x}Zr{sub 0.1}Cu{sub x}O{sub 3} (x = 0.2, 0.4, 0.6, 0.8 and 1%) ceramics were prepared from nanopowders using a hydrothermal method. • The ceramic samples had high dielectric constant. • The ceramic samples showed a fine ferroelectric hysteresis loop. • The piezoelectric charge coefficient (d{sub 33}) of BCZTC ceramics was improved with Cu doping. - Abstract: Ba{sub 0.85}Ca{sub 0.15}Ti{sub 0.9}Zr{sub 0.1−x}Cu{sub x}O{sub 3} (BCTZC) nanopowders were synthesized using a hydrothermal method after which they were pressed into discs and sintered in air at 1300 °C for 3 h to form ceramic samples. The phase and microstructure of the powder and ceramic samples were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The XRD results indicated that the ceramic samples exhibited a tetragonal structure and that CuO, BaZrO{sub 3} or CaTiO{sub 3} impurity phases, which had been present in the powder samples, were not observed. The average grain sizes in the ceramic samples were found to be 17.0, 16.1, 20.0, 18.1 and 19.6 μm for Cu mole fractions x of 0.002, 0.004, 0.006, 0.008 and 0.01, respectively. The dielectric constants, ferroelectric hysteresis loops and piezoelectric charge coefficients of the BCZTC ceramic samples were also investigated. Optimum values for the relative dielectric constant (ε′), tan δ and piezoelectric charge coefficient (d{sub 33}) of the samples were 3830, 0.03 and 306 p

  4. Synthesized TiO{sub 2}/ZSM-5 composites used for the photocatalytic degradation of azo dye: Intermediates, reaction pathway, mechanism and bio-toxicity

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Kefu; Hu, Xin-Yan [College of the Environment and Ecology, Xiamen University, Xiamen (China); Chen, Bor-Yann; Hsueh, Chung-Chuan [Department of Chemical and Materials Engineering, National I-Lan University, I-Lan, Taiwan (China); Zhang, Qian [Department of Environmental Engineering, National Taiwan University, Taipei, Taiwan (China); Wang, Jiajie; Lin, Yu-Jung [College of the Environment and Ecology, Xiamen University, Xiamen (China); Chang, Chang-Tang, E-mail: ctchang73222@gmail.com [Department of Environmental Engineering, National I-Lan University, I-Lan, Taiwan (China)

    2016-10-15

    Highlights: • The major photo-catalytic degradation pathway of azo-dye was elaborated according to the identification of by-products from GC–MS and IC analysis. • Comparative assessment on characteristics of abiotic and biotic dye decolorization was analyzed. • EDTA (hole scavengers) and t-BuOH (radical scavengers) were used to determine the main active oxidative species in the system. • The toxicity effects of degradation intermediates of Reactive Black 5 (RB5) on the cellular respiratory activity were assessed. - Abstract: In this study, a one-step solid dispersion method was used to synthesize titanium dioxide (TiO{sub 2})/Zeolite Socony Mobil-5 (ZSM-5) composites with substantially reduced time and energy consumption. A degradation efficiency of more than 95% was achieved within 10 min using 50% PTZ (synthesized TiO{sub 2}/ZSM-5 composites with TiO{sub 2} contents of 50 wt% loaded on ZSM-5) at pH 7 and 25 °C. The possible degradation pathway of azo-dye Reactive Black 5 (RB5) was investigated using gas chromatography–mass spectrometry and ion chromatography (IC). The bonds between the N atoms and naphthalene groups are likely attacked first and cleaved by hydroxyl radicals, ultimately resulting in the decolorization and mineralization of the azo dye. A comparative assessment of the characteristics of abiotic and biotic dye decolorization was completed. In addition, the toxicity effects of the degradation intermediates of azo-dye RB5 on cellular respiratory activity were analyzed. The bio-toxicity results showed that the decay rate constants of CO{sub 2} production from the azo-dye RB5 samples at different degradation times increased initially and subsequently decreased, indicating that intermediates of higher toxicity could adhere to the catalyst surface and gradually destroyed by further photocatalytic oxidation. Additionally, EDTA (hole scavengers) and t-BuOH (radical scavengers) were used to detect the main active oxidative species in the system

  5. Evolving patterns of the fluids within the TAG hydrothermal field

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The mixing of seawater/hydrothermal fluid within the large seafloor hydrothermal sulfide deposits plays a key role in the formation processes of the sulfide deposits.Some issues attract considerable attentions in the study of seafloor hydrothermal system in recent years,such as the relationships among different types of vent fluids,the characteristics of chemical compositions and mineral assemblages of the hydrothermal deposits and their governing factors.Combined with the measured data of hydrothermal fluid in the TAG field,the thermodynamic model of mixing processes of the heated seawater at different temperatures and the hydrothermal fluid is calculated to understand the precipitation mechanism of anhydrite and the genetic relationships between the black and white smoker fluids within the TAG mound.The results indicate that the heating of seawater and the mixing of hydrothermal fluid/seawater are largely responsible for anhydrite precipitation and the temperature of the heated seawater is not higher than 150 ℃ and the temperature of the end-member hydrothermal fluid is not lower than 400℃.Based on the simulated results,the evolving patterns of fluids within the TAG deposit are discussed.The mixed fluid of the end-member hydrothermal fluid and the seawater heated by wall rock undergoes conductive cooling during upflowing within the deposit and forms "White Smoker" eventually.In addition,the end-member hydrothermal fluid without mixed with seawater,but undergoing conductive cooling,vents out of the deposit and forms "Black Smoker".

  6. PREPARATION OF LEUCITE-BASED COMPOSITES

    Directory of Open Access Journals (Sweden)

    Alexandra Kloužková

    2012-12-01

    Full Text Available The aim of this study was to prepare leucite dental composites from two separately synthesized components - tetragonal leucite and glassy matrix. The newly developed procedure is based on the preparation of crystalline tetragonal leucite powder by relatively low temperature synthesis under hydrothermal conditions. Matrix powder was prepared by a classical melting process and subsequent milling of the quenched glass. The dental composites were prepared by mixing of 10 wt. %, 20 wt. % and 30 wt. % of synthesized tetragonal leucite with glass powder followed by pressing and firing. The sintering process was observed by optical microscope and the optimal firing temperature for each composite was determined. Optical and electron microscopy was used to characterise the microstructure of the composites, especially the distribution of the leucite particles in the matrix. Dilatometric measurements proved that the coefficient of thermal expansion of the composites increased up to 44 % in comparison with the basic matrix.

  7. Hydrothermal pretreatment of palm oil empty fruit bunch

    Science.gov (United States)

    Simanungkalit, Sabar Pangihutan; Mansur, Dieni; Nurhakim, Boby; Agustin, Astrid; Rinaldi, Nino; Muryanto, Fitriady, Muhammad Ariffudin

    2017-01-01

    Hydrothermal pretreatment methods in 2nd generation bioethanol production more profitable to be developed, since the conventional pretreatment, by using acids or alkalis, is associated with the serious economic and environmental constraints. The current studies investigate hydrothermal pretreatment of palm oil empty fruit bunch (EFB) in a batch tube reactor system with temperature and time range from 160 to 240 C and 15 to 30 min, respectively. The EFB were grinded and separated into 3 different particles sizes i.e. 10 mesh, 18 mesh and 40 mesh, prior to hydrothermal pretreatment. Solid yield and pH of the treated EFB slurries changed over treatment severities. The chemical composition of EFB was greatly affected by the hydrothermal pretreatment especially hemicellulose which decreased at higher severity factor as determined by HPLC. Both partial removal of hemicellulose and migration of lignin during hydrothermal pretreatment caused negatively affect for enzymatic hydrolysis. This studies provided important factors for maximizing hydrothermal pretreatment of EFB.

  8. Formation of hydrothermal biochar and char stability in soils

    Science.gov (United States)

    Baumert, Julia; Gleixner, Gerd

    2010-05-01

    The use of charcoal as an artificial soil additive is suggested to beneficially modify degraded soil, reduce greenhouse gas emission and improve crop yields. So far research has been mainly done using pyrolysis chars which are produced by dry pyrolysis of biomass. Here we used hydrothermal carbonisation (HTC). In this process wet biomass is converted to char at moderate temperatures (~200°C). Due to the exothermal carbonisation reaction this process is almost energy neutral, i.e. the energy needed to start the carbonisation equals the energy released during carbonisation. Different process parameters have been used to modify the properties of the produced chars. We examined the chemical and morphological properties of hydrothermally synthesized biochar. Cellulose, yeast and sucrose were used as model substances for a range of parent material types like organic and garden waste as well as residues from biogas production. By modifying the process conditions of hydrothermal carbonisation concerning temperature (180°C to 220°C) and duration (6 hours to 24 hours) we produced a variety of different biochars. Our findings suggest that the elemental composition and the thermal stability of resulting chars depend on the feedstock and production conditions. Functional group chemistry determined by NMR shows that the aromaticity of the product increases as a function of temperature whereas the amount of O-alkylic compounds declines, concurrently. Our results show that the properties of the biochar can be manipulated by the modification of process conditions. This opens the opportunity to adjust the charcoal to a given soil type.

  9. One-pot hydrothermal synthesis of CuS/C composite and its application in supercapacitors%“一锅法”水热制备CuS/C复合材料及其在超级电容器中的应用

    Institute of Scientific and Technical Information of China (English)

    赵双生; 应宗荣; 杨佳佳; 凡川

    2016-01-01

    采用三水合硝酸铜为铜源、硫脲为硫源、D-葡萄糖酸钠为络合剂,发展了简单的“一锅法”水热直接一步合成CuS/C复合材料。采用X射线衍射仪(XRD)、激光显微拉曼光谱仪(Raman)、扫描电子显微镜(SEM)和有机元素分析仪对复合材料组成、结构及形貌进行表征。研究发现,样品主要由花状CuS球组成,同时含有质量分数约为6%的光滑炭球,CuS 球表面分布有花瓣状褶皱,形成的大量孔道有利于离子传输,并增大活性物质与电解液的接触面积。研究表明,在1 A·g−1电流密度下,比电容高达719 F·g−1,与不加络合剂制备得到的CuS (382 F·g−1)相比,比电容显著提高,并且在充放电1000次后比电容保持在80%左右,显示出良好的循环稳定性。%In this work, a simple one-pot hydrothermal method was developed to synthetize CuS/C composite in one-step by using copper nitrate trihydrate (Cu(NO3)2·3H2O) as copper source, thiourea as sulfur source and D-glucose sodium as complexing agent. The composition, microstructure and morphology of the CuS/C composite were characterized by X ray diffraction (XRD), Raman spectroscopy, organic element analyzer and scanning electron microscopy (SEM). It was found that the as-synthesized composite was mainly composed of novel petaloid CuS microspheres, which provided many paths for ion diffusion and increased specific area with about 6% of amorphous carbon microspheres (mass fraction). The composite exhibited a maximum specific capacitance of up to 719 F·g−1 at 1 A·g−1, while the specific capacitance was 382F·g−1 at 1 A·g−1 for CuSprepared without using complexing agent. The long-term constant current charge-discharge test showed that the CuS/C composite exhibited excellent long cycle life with capacitance retention of 80% after 1000 cycles at 1 A·g−1. Although due to low melting point (220℃) of CuS, heat treatment at high

  10. Effect of Synthesis Parameters on the Structure and Magnetic Properties of Magnetic Manganese Ferrite/Silver Composite Nanoparticles Synthesized by Wet Chemistry Method

    DEFF Research Database (Denmark)

    Huy, L.T.; Tam, L.T.; Phan, V.N.

    2016-01-01

    In the present work, magnetic manganese ferrite/silver (MnFe2O4-Ag) composite nanoparticles were synthesized by wet chemistry method. This synthesis process consists of two steps: first, the seed of manganese ferrite nanoparticles (MnFe2O4 NPs) was prepared by a coprecipitationmethod; second......, growth of silver nanoparticles (AgNPs) on the MnFe2O4 seed by modified photochemical reaction. We have conducted systematically the effects of synthesis parameters such as pH value, synthesis time, precursor salts concentration, mass ratio and stabilizing agents on the structure and magnetic properties...... of nanocomposites. In an optimized condition of synthesis parameters, the high quality MnFe2O4 NPs are obtained at pH value = 13, Mn2+ cation concentration= 0.4 M and synthesis time about 105 min; and the use of PVP stabilizing agent is found to optimize the formation of Ag-NPs on the surface of MnFe2O4 NPs. The as...

  11. A microwave synthesized CuxS and graphene oxide nanoribbon composite as a highly efficient counter electrode for quantum dot sensitized solar cells.

    Science.gov (United States)

    Ghosh, Dibyendu; Halder, Ganga; Sahasrabudhe, Atharva; Bhattacharyya, Sayan

    2016-05-19

    To boost the photoconversion efficiency (PCE) of ever promising quantum dot sensitized solar cells (QDSSCs), and to improve the design of photoanodes, the ability of the counter electrode (CE) to effectively reduce the oxidized electrolyte needs special attention. A composite of a 15 wt% graphene oxide nanoribbon (GOR), obtained by unzipping multi-walled carbon nanotubes (MWCNTs), and CuxS intersecting hexagonal nanoplates, synthesized by a low cost, facile and scalable microwave synthesis route, is reported as a fascinating CE for QDSSCs. The best performing Cu1.18S-GOR CE could notably achieve a record PCE of ∼3.55% for CdS sensitized QDSSCs, ∼5.42% for in situ deposited CdS/CdSe co-sensitized QDSSCs and ∼6.81% for CdTe/CdS/CdS dual sensitized QDSSCs, apart from increasing the PCE of previously reported QDSSCs. A systematic investigation of the CE design revealed the high electrocatalytic activity of GOR due to the presence of organic functional groups, graphitic edge sites and a quasi-one-dimensional (quasi-1D) structure, which increases the interfacial charge transfer kinetics from the CE to the polysulfide electrolyte. The highly stable Cu1.18S-GOR CE has the added advantage of a favourable energy band alignment with the redox potential of the polysulfide electrolyte, which reduces the loss of charge carriers and thus can increase the PCE of QDSSCs.

  12. Effect of Zircon Silicate Reinforcements on the Microstructure and Properties of as Cast Al-4.5Cu Matrix Particulate Composites Synthesized via Squeeze Cast Route

    Directory of Open Access Journals (Sweden)

    E. G. Okafor

    2010-06-01

    Full Text Available The as-cast microstructure and properties of Al-4.5Cu/ZrSiO4 particulate composite synthesized via squeezed casting route was studied, varying the percentage ZrSiO4 in the range of 5-25wt%. The result obtained revealed that addition of ZrSiO4 reinforcements, increased the hardness value and apparent porosity by 107.65 and 34.23% respectively and decrease impact energy by 43.16 %. As the weight percent of ZrSiO4 increases in the matrix alloy, the yield and ultimate tensile strength increased by 156.52 and 155.81% up to a maximum of 15% ZrSiO4 addition respectively. The distribution of the brittle ZrSiO4 phase in the ductile matrix alloy led to increase strength and hardness values. These results had shown that, additions of ZrSiO4 particles to Al-4.5Cu matrix alloy improved properties.

  13. Microstructural characterization of titanium matrix composite coatings reinforced by in situ synthesized TiB + TiC fabricated on Ti6Al4V by laser cladding

    Institute of Scientific and Technical Information of China (English)

    LI Jun; YU Zhishui; WANG Huiping; LI Manping

    2010-01-01

    Titanium-based composite coatings reinforced by in situ synthesized TiB and TiC particles between titanium and B4C were successfully fab-ricated on Ti6A14V by laser cladding. Phase constituents of the coatings were predicted by thermodynamic calculations in the Ti-B4C-Al and Ti-B-C-Al systems, respectively, and were validated well by X-ray diffraction (XRD) analysis results. Microstructural and metallographic analyses were made by scanning electron microscopy (SEM) and electron probe micro-analysis (EPMA). The results show that the coatings are mainly composed of α-Ti cellular dendrites and the eutecticum in which a large number of needle-shaped TiB and a few equiaxial TiC particles are embedded. C is enriched in α-Ti cellular dendrites and far exceeds the theoretical maximum dissolubility, owing to the extension of saturation during laser cladding. The coatings have a good metallurgical bond with the substrate due to the existence of the dilution zone, in which a great amount of lamella β-Ti grains consisting of a thin needle-shaped martensitic microstructurc are present and grow parallel to the heat flux direction; a few TiB and TiC reinforcements are observed at the boundaries of initial β-Ti grains.

  14. Microstructure and Tribological Properties of In-situ Synthesized TiB2-TiC/Ni Based Composite Coating by Laser Cladding

    Institute of Scientific and Technical Information of China (English)

    SUNRong-lu; TANGYing; YANGXian-jin

    2004-01-01

    A TiB2 and TiC particles reinforced Ni based composites coating was prepared on TC4 alloy surface by chemical reaction among Ti, B and C elements using laser cladding technique. Microstructural analysis showed that the sizes of in-situ synthesized TiB2 and TiC particles ranged within 5-10μm and 1-2μm, respectively, while both the two kinds of particles were uniformly distributed in the clad layer. The measurement of microhardness and wear and friction propert iesindicated that the microhardness of laser clad layer was HV900-1100, being three times of that of the TC4 alloy; the friction coefficient of the laser clad layer in air and in vacuum (10-5Pa) ranged within 0.2-0.3 and 0.3-0.5, respectively; the wear rate in terms of mass loss was considerably lower than that of the TC4 alloy both in air and in vacuum environment.

  15. Microstructure and Tribological Properties of In-situ Synthesized TiB2- TiC/Ni Based Composite Coating by Laser Cladding

    Institute of Scientific and Technical Information of China (English)

    SUN Rong-lu; TANG Ying; YANG Xian-jin

    2004-01-01

    ATiB2 and TiC particles reinforced Ni based composites coating was prepared on TC4 alloy surface by chemical reaction among Ti, B and C elements using laser cladding technique. Microstructural analysis showed that the sizes of in-situ synthesized TiB2 and TiC particles ranged within 5~10μm and 1~2μn, respectively, while both the two kinds of particles were uniformly distributed in the clad layer. The measurement of microhardness and wear and friction properties indicated that the microhardness of laser clad layer was HV900~1100, being three times of that of the TC4 alloy; the friction coefficient of the laser clad layer in air and in vacuum (10-5 Pa) ranged within 0.2~0.3 and 0.3~0.5, respectively; the wear rate in terms of mass loss was considerably lower than that of the TC4 alloy both in air and in vacuum environment.

  16. Investigations of the capacity of synthesizing 3β-sterols in mollusca—VI. The biosynthesis and composition of 3β-sterols in the neogastropods Purpura lapillus and Murex brandaris

    NARCIS (Netherlands)

    Voogt, P.A.

    1972-01-01

    1. 1. It is shown that Purpura lapillus and Murex brandaris are capable of synthesizing sterols from mevalonate and acetate. The biosynthesis of sterols from acetate proceeds only at a slow rate. This phenomenon is compared with that observed in Natica cataena. 2. 2. The composition of the sterol m

  17. Investigations of the capacity of synthesizing 3β-sterols in mollusca—VI. The biosynthesis and composition of 3β-sterols in the neogastropods Purpura lapillus and Murex brandaris

    NARCIS (Netherlands)

    Voogt, P.A.

    1972-01-01

    1. 1. It is shown that Purpura lapillus and Murex brandaris are capable of synthesizing sterols from mevalonate and acetate. The biosynthesis of sterols from acetate proceeds only at a slow rate. This phenomenon is compared with that observed in Natica cataena. 2. 2. The composition of the sterol m

  18. Preparation of silver tin oxide powders by hydrothermal reduction and crystallization

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Silver tin oxide composite powders were synthesized by the hydrothermal method with a silver ammine solution and a Na2SnO3 solution as raw marrials. H2C2O4 was used as the co-precipitator of silver ions and tin ions. The co-precipitation conditions were investigated. The results show that the co-precipitate of Ag2C2O4 and Sn(OH)4 is available when the pH value of the solution is 4.27-8.36. Using the obtained precipitate as precursor, the reduction of Ag+ and the crystallization of tin oxide were carried out simultaneonsly by the hydrothermal method and silver tin oxide composite powders were obtained. The composite powders were characterized by X-ray diffraction (XRD) analysis, scanning electron microscope (SEM), and energy spectrum analysis. The results show that the silver tin oxide composite powders are small with a diameter of about 2 μm and with homogeneous distribution of tin.

  19. Hydrothermal synthesis of xonotlite from carbide slag

    Institute of Scientific and Technical Information of China (English)

    Jianxin Cao; Fei Liu; Qian Lin; Yu Zhang

    2008-01-01

    Carbide slag was used as the calcareous materials for the first time to prepare xonotlite via dynamic hydrothermal synthesis.The effects of influential factors including different calcination temperatures,pretreatment methods of the carbide slag and process param-eters of hydrothermal synthesis on the microstructure and morphology of xonotlite were explored using XRD and SEM techniques.The results indicate that the carbide slag after proper calcination could be used to prepare pure xonotlite;and different calcination tern-peratures have little effect on the crystallinity of synthesized xonotlitc,but have great impact on the morphology of secondary particles.The different pretreatment methods of the carbide slag pose great impact on the crystallinity and morphology of secondary particles of xonotlite.Xonotlite was also synthesized from pure CaO under the salne experimental conditions as that prepared from calcined carbide slag for comparison.Little amount of impurities in carbide slag has no effect on the mechanism of hydrothermal synthesizing xonotlite from carbide slag.

  20. Highly Crystalline FeCO3 Microparticle Synthesis by Hydrothermal Decomposition of Fe-EDTA Complex

    Science.gov (United States)

    Chirita, M.; Banica, R.; Ieta, A.; Bucur, A.; Sfiarloaga, P.; Ursu, D. H.; Grozescu, I.

    2010-08-01

    In this article, we present an experimental procedure to synthesize highly crystalline FeCO3 by hydrothermal decomposition of Fe(III)-EDTA complex, starting from Ferric Ammonium Sulfate and Na4EDTA main precursors in urea presence. The structure, morphology and composition of the powders were obtained using X-ray powder diffraction and scanning electron microscopy. The peaks were founded, indicate that the synthesized products autoclaved 22 h at 250 °C are pure FeCO3, which was well proved experimentally from EDAX further investigated. The size with appreciatively 100 μm was evaluated by SEM images. Magnetic characterization confirmed the magnetic characteristics of FeCO3. This procedure allowed the FeCO3 microparticles formation with good and stabile crystallographic characteristics.

  1. Solubility limits in Mn–Mg ferrites system under hydrothermal conditions

    Energy Technology Data Exchange (ETDEWEB)

    Hemeda, O.M., E-mail: omhemeda@yahoo.co.uk [Physics Department, Faculty of Science, Tanta University, Tanta (Egypt); Mostafa, N.Y. [Chemistry Department, Faculty of Science, Suez Canal University, Ismailia 41522 (Egypt); Faculty of Science, Taif University, PO Box 888, Al-Haweiah, Taif (Saudi Arabia); Abd Elkader, O.H. [Electron Microscope and Thin Films Department, National Research Center, Dokki 12622, Cairo (Egypt); Electron Microscope Unit, Zoology Department, King Saud University, Riyadh 11451 (Saudi Arabia); Ahmed, M.A. [Physics Department, Faculty of Science, Al Azhar University, Nasr City, Cairo (Egypt)

    2014-09-01

    In the present investigation, we successfully synthesized a pure MnFe{sub 2}O{sub 4} ferrite by the hydrothermal method. Moreover, the effect of Mg ion content on the formation of Mn{sub 1−x}Mg{sub x}Fe{sub 2}O{sub 4} particles (with x varying from 0.1 to 1.0) was also investigated using XRD, SEM, TEM and Mossbauer Spectroscopy. Phases formed in the system Mn{sub 1−x}Mg{sub x}Fe{sub 2}O{sub 4}; 0.0≤x≤1.0 were investigated under hydrothermal conditions at 453 K.The produced phases were characterized by X-ray diffraction, Scanning, transmission microscopy and Mossbauer spectroscopy. The information of composition, cation distribution in the spinel structure and the particle size of the products were obtained. The spinel ferrites; Mn{sub 1−x}Mg{sub x}Fe{sub 2}O{sub 4} were formed in the range 0.0≤x≤0.3. However, sample with x>0.3 showed semi-crystalline magnesium hydroxide (Mg(OH){sub 2}) and hematite (Fe{sub 2}O{sub 3}) beside the ferrite phase. For x=1.0, only magnesium hydroxide and hematite are formed without any ferrites. Particles of uniform size around 10–20 nm were obtained in the spinel structure of Mn{sub 1−x}Mg{sub x}Fe{sub 2}O{sub 4} with x=0.0 and 0.1. The corresponding average crystallite size for each sample was 40.3 nm and 39.2 nm respectively. In addition, the Mossbauer spectra were analyzed into two subspectra, one for the tetrahedral A-site and the other for the octahedral B-site. The Mossbauer parameters were determined and discussed for the studied system. The cation distribution was estimated from the analysis of the Mossbauer spectra as well as the X-ray diffraction patterns. The results showed that Mg ions occupy mainly B-site while both Mn and Fe ions are distributed between A- and B-sites. - Highlights: • Mossbauer characterization of Mg–Mn ferrite prepared by hydrothermal route. • X-ray powder diffraction analysis of Mg–Mn ferrite prepared by hydrothermal route. • Solubility limit of MgMn ferrite under

  2. A microwave synthesized CuxS and graphene oxide nanoribbon composite as a highly efficient counter electrode for quantum dot sensitized solar cells

    Science.gov (United States)

    Ghosh, Dibyendu; Halder, Ganga; Sahasrabudhe, Atharva; Bhattacharyya, Sayan

    2016-05-01

    To boost the photoconversion efficiency (PCE) of ever promising quantum dot sensitized solar cells (QDSSCs), and to improve the design of photoanodes, the ability of the counter electrode (CE) to effectively reduce the oxidized electrolyte needs special attention. A composite of a 15 wt% graphene oxide nanoribbon (GOR), obtained by unzipping multi-walled carbon nanotubes (MWCNTs), and CuxS intersecting hexagonal nanoplates, synthesized by a low cost, facile and scalable microwave synthesis route, is reported as a fascinating CE for QDSSCs. The best performing Cu1.18S-GOR CE could notably achieve a record PCE of ~3.55% for CdS sensitized QDSSCs, ~5.42% for in situ deposited CdS/CdSe co-sensitized QDSSCs and ~6.81% for CdTe/CdS/CdS dual sensitized QDSSCs, apart from increasing the PCE of previously reported QDSSCs. A systematic investigation of the CE design revealed the high electrocatalytic activity of GOR due to the presence of organic functional groups, graphitic edge sites and a quasi-one-dimensional (quasi-1D) structure, which increases the interfacial charge transfer kinetics from the CE to the polysulfide electrolyte. The highly stable Cu1.18S-GOR CE has the added advantage of a favourable energy band alignment with the redox potential of the polysulfide electrolyte, which reduces the loss of charge carriers and thus can increase the PCE of QDSSCs.To boost the photoconversion efficiency (PCE) of ever promising quantum dot sensitized solar cells (QDSSCs), and to improve the design of photoanodes, the ability of the counter electrode (CE) to effectively reduce the oxidized electrolyte needs special attention. A composite of a 15 wt% graphene oxide nanoribbon (GOR), obtained by unzipping multi-walled carbon nanotubes (MWCNTs), and CuxS intersecting hexagonal nanoplates, synthesized by a low cost, facile and scalable microwave synthesis route, is reported as a fascinating CE for QDSSCs. The best performing Cu1.18S-GOR CE could notably achieve a record PCE of ~3

  3. Physical and gas permeation properties of a series of novel hybrid inorganic-organic composites based on a synthesized fluorinated polyimide

    Science.gov (United States)

    Cornelius, Christopher James

    2000-11-01

    A series of hybrid inorganic-organic composites were fabricated from a functionalized fluorinated polyimide and tetraethoxysilane (TEOS), tetramethoxysilane, methyltrimethoxysilane (MTMOS), and phenyltrimethoxy-silane (PTMOS) employing the sol-gel process. Polyimides were synthesized from 4,4'-hexafluoroisopropylidene dianiline (6FpDA) and 4,4'-hexafluoroisopropyl-idenediphthalic anhydride (6FDA) utilizing a solution imidization technique. The hybrid materials were synthesized by in-situ sol-gel processing of the aforementioned alkoxides and a fully imidized polyimide that was functionalized with 3-aminopropyltriethoxysilane. The gas permeability, diffusivity, and selectivity were evaluated for He, O2, N2, CH4, and CO2, while the physical properties of these hybrid materials were evaluated using several analytical techniques. The results from this study revealed that gas transport and physical properties were dependent on the type of alkoxide employed in the hybrid inorganic-organic material. Gas permeability was observed to increase with increasing gas penetrant size for MTMOS and PTMOS based hybrids, while TEOS based hybrids decreased gas permeability at all compositions. In general, MTMOS based hybrid materials had the largest increases in permeability, which was attributed to an increase in free volume. The TEOS based hybrid materials had the largest decreases in permeability, while PTMOS based hybrid materials had performance in between these alkoxides. Decreased permeability for the TEOS based hybrids was attributed to the formation of lower permeable material at a particle interface and coupled with increasing tortuosity. Results of PALS studies suggested that there was an increase in free volume and pore size for MTMOS based hybrids, while both TEOS and PTMOS based hybrids had decreases in both average pore size and free volume. The temperature dependence of permeation, diffusivity, and sorption were evaluated from 35°C to 125°C. These results suggested

  4. Dietary supplementation of green synthesized manganese-oxide nanoparticles and its effect on growth performance, muscle composition and digestive enzyme activities of the giant freshwater prawn Macrobrachium rosenbergii.

    Science.gov (United States)

    Asaikkutti, Annamalai; Bhavan, Periyakali Saravana; Vimala, Karuppaiya; Karthik, Madhayan; Cheruparambath, Praseeja

    2016-05-01

    The green synthesized Mn3O4 nanoparticles (manganese-oxide nanoparticles) using Ananas comosus (L.) peel extract was characterized by various techniques. HR-SEM photograph showed that manganese-oxide nanoparticles (Mn-oxide NPs) were spherical in shape, with an average size of 40-50 nm. The Zeta potential revealed the surface charge of Mn-oxide NPs to be negative. Further, the Mn-oxide NPs were dietary supplemented for freshwater prawn Macrobrachium rosenbergii. The experimental basal diets were supplemented with Mn-oxide NPs at the rates of 0 (control), 3.0, 6.0, 9.0, 12, 15 and 18 mg/kg dry feed weight. The as-supplemented Mn-oxide NPs were fed in M. rosenbergii for a period of 90 days. The experimental study demonstrated that prawns fed with diet supplemented with 3-18 mg Mn-oxide NPs/kg shows enhanced (Pgrowth performance, including final weight and weight gain (WG). Significant differences (Pgrowth performance, digestive enzyme activities and muscle biochemical compositions, while, the prawns fed with 16 mg/kg of Mn-oxide NPs showed enhanced performance. Prawns fed on diet supplemented with 16 mg/kg Mn-oxide NPs showed significantly (Pmuscle and hepatopancreas showed no significant (P>0.05) alterations in prawns fed with 3.0-18 mg/kg of Mn-oxide NPs supplemented diets. Consequently, the present work proposed that 16 mg/kg of Mn-oxide NPs could be supplemented for flexible enhanced survival, growth and production of M. rosenbergii. Therefore, the data of the present study recommend the addition of 16 mg/kg of Mn-oxide NPs diet to developed prawn growth and antioxidant defense system. Copyright © 2016 Elsevier GmbH. All rights reserved.

  5. Hydrothermal alteration in oceanic ridge volcanics: A detailed study at the Galapagos Fossil Hydrothermal Field

    Science.gov (United States)

    Ridley, W.I.; Perfit, M.R.; Josnasson, I.R.; Smith, M.F.

    1994-01-01

    The Galapagos Fossil Hydrothermal Field is composed of altered oceanic crust and extinct hydrothermal vents within the eastern Galapagos Rift between 85??49???W and 85??55???W. The discharge zone of the hydrothermal system is revealed along scarps, thus providing an opportunity to examine the uppermost mineralized, and highly altered interior parts of the crust. Altered rocks collected in situ by the submersible ALVIN show complex concentric alteration zones. Microsamples of individual zones have been analysed for major/minor, trace elements, and strontium isotopes in order to describe the complex compositional details of the hydrothermal alteration. Interlayered chlorite-smectite and chlorite with disequilibrium compositions dominate the secondary mineralogy as replacement phases of primary glass and acicular pyroxene. Phenocrysts and matrix grains of plagioclase are unaffected during alteration. Using a modification of the Gresens' equation we demonstrate that the trivalent rare earth elements (REEs) are relatively immobile, and calculate degrees of enrichment and depletion in other elements. Strontium isotopic ratios increase as Sr concentrations decrease from least-altered cores to most-altered rims and cross-cutting veins in individual samples, and can be modeled by open system behaviour under low fluid-rock ratio (metal sulfides beneath the seafloor is probably a result of fluid mixing and cooling. If, as suggested here, the discharge zone alteration occurred under relatively low fluid-rock ratios, then this shallow region must play an important role in determining the exit composition of vent fluids in marine hydrothermal systems. ?? 1994.

  6. Theoretical constraints of physical and chemical properties of hydrothermal fluids on variations in chemolithotrophic microbial communities in seafloor hydrothermal systems

    Science.gov (United States)

    Nakamura, Kentaro; Takai, Ken

    2014-12-01

    In the past few decades, chemosynthetic ecosystems at deep-sea hydrothermal vents have received attention as plausible analogues to the early ecosystems of Earth, as well as to extraterrestrial ecosystems. These ecosystems are sustained by chemical energy obtained from inorganic redox substances (e.g., H2S, CO2, H2, CH4, and O2) in hydrothermal fluids and ambient seawater. The chemical and isotope compositions of the hydrothermal fluid are, in turn, controlled by subseafloor physical and chemical processes, including fluid-rock interactions, phase separation and partitioning of fluids, and precipitation of minerals. We hypothesized that specific physicochemical principles describe the linkages among the living ecosystems, hydrothermal fluids, and geological background in deep-sea hydrothermal systems. We estimated the metabolic energy potentially available for productivity by chemolithotrophic microorganisms at various hydrothermal vent fields. We used a geochemical model based on hydrothermal fluid chemistry data compiled from 89 globally distributed hydrothermal vent sites. The model estimates were compared to the observed variability in extant microbial communities in seafloor hydrothermal environments. Our calculations clearly show that representative chemolithotrophic metabolisms (e.g., thiotrophic, hydrogenotrophic, and methanotrophic) respond differently to geological and geochemical variations in the hydrothermal systems. Nearly all of the deep-sea hydrothermal systems provide abundant energy for organisms with aerobic thiotrophic metabolisms; observed variations in the H2S concentrations among the hydrothermal fluids had little effect on the energetics of thiotrophic metabolism. Thus, these organisms form the base of the chemosynthetic microbial community in global deep-sea hydrothermal environments. In contrast, variations in H2 concentrations in hydrothermal fluids significantly impact organisms with aerobic and anaerobic hydrogenotrophic metabolisms

  7. Sol-Gel-Hydrothermal Synthesis of the Heterostructured TiO2/N-Bi2WO6 Composite with High-Visible-Light- and Ultraviolet-Light-Induced Photocatalytic Performances

    Directory of Open Access Journals (Sweden)

    Jiang Zhang

    2012-01-01

    Full Text Available The heterostructured TiO2/N-Bi2WO6 composites were prepared by a facile sol-gel-hydrothermal method. The phase structures, morphologies, and optical properties of the samples were characterized by using X-ray powder diffraction (XRD, scanning electron microscopy (SEM, high-resolution transmission electron microscopy (HRTEM, energy dispersive spectroscopy (EDS, and UV-vis diffuse reflectance spectroscopy. The photocatalytic activities for rhodamine B of the as-prepared products were measured under visible and ultraviolet light irradiation at room temperature. The TiO2/N-Bi2WO6 composites exhibited much higher photocatalytic performances than TiO2 as well as Bi2WO6. The enhancement in the visible light photocatalytic performance of the TiO2/N-Bi2WO6 composites could be attributed to the effective electron-hole separations at the interfaces of the two semiconductors, which facilitate the transfer of the photoinduced carriers.

  8. MATHEMATICAL MODELLING OF HYDROTHERMAL GROWTH OF CRYSTALS AS A DOUBLE DIFFUSIVE MAGNETOCONVECTION PROBLEM IN A COMPOSITE LAYER BOUNDED BY RIGID WALLS.

    Directory of Open Access Journals (Sweden)

    R. Sumithra

    2012-02-01

    Full Text Available The Hydrothermal growth of crystals is mathematically modeled as the onset of double diffusive magnetoconvection in a two-layer system comprising an incompressible two component, electrically conducting fluid saturated porous layer over which lies a layer of the same fluid in the presence a vertical magnetic field. Both the upper boundary of the fluid layer and the lower boundary of the porous layer are rigid and insulating to both heat and mass. At the interface the velocity, shear stress, normal stress, heat, heat flux,mass and mass flux are assumed to be continuous conducive for Darcy-Brinkman model. The resulting eigenvalue problem is solved by regular perturbation technique. The critical Rayleigh number, which is thecriterion for stability of the system is obtained. The effects of different physical parameters on the onset of double diffusive magnetoconvection are investigated in detail which enables to control convection during the growth of crystals in order to obtain pure crystals.

  9. Evaluation of Hydrothermally Synthesized Uranium Dioxide for Novel Semiconductor Applications

    Science.gov (United States)

    2016-08-29

    radiation detectors. In the age of high-tech, miniaturized devices, the end-user expects a radiation detector to be compact, portable, consume little...with data mining to provide details about movements of radiation sources. To achieve this, detectors must be small, simple, low power consumers , and...work function, φm, and the electron affinity of the semiconductor, Xs. The Schottky-Mott equations describe this relationship which is often

  10. Peptide synthesis in early earth hydrothermal systems

    Science.gov (United States)

    Lemke, K.H.; Rosenbauer, R.J.; Bird, D.K.

    2009-01-01

    We report here results from experiments and thermodynamic calculations that demonstrate a rapid, temperature-enhanced synthesis of oligopeptides from the condensation of aqueous glycine. Experiments were conducted in custom-made hydrothermal reactors, and organic compounds were characterized with ultraviolet-visible procedures. A comparison of peptide yields at 260??C with those obtained at more moderate temperatures (160??C) gives evidence of a significant (13 kJ ?? mol-1) exergonic shift. In contrast to previous hydrothermal studies, we demonstrate that peptide synthesis is favored in hydrothermal fluids and that rates of peptide hydrolysis are controlled by the stability of the parent amino acid, with a critical dependence on reactor surface composition. From our study, we predict that rapid recycling of product peptides from cool into near-supercritical fluids in mid-ocean ridge hydrothermal systems will enhance peptide chain elongation. It is anticipated that the abundant hydrothermal systems on early Earth could have provided a substantial source of biomolecules required for the origin of life. Astrobiology 9, 141-146. ?? 2009 Mary Ann Liebert, Inc. 2009.

  11. A Novel Polymer-Synthesized Ceramic Composite Based System for Bone Repair: Osteoblast Growth on Scaffolds with Varied Calcium Phosphate Content

    Science.gov (United States)

    2005-01-01

    demongtrated the synthesis of degradable scaffolds from PLAGA /calcium phosphate composite microspheres in which an amorphous calcium phosphate is...EXPERIMENTAL DETAILS Scaffold Preparation Scaffolds were prepared as described in detail previously [3]. Briefly, PLAGA /calcium phosphate composite...culture polystyrene (TCPS) 2- pure PLAGA microspheres 64 3- composite microsphere matrices with a low polymer/ceramic ratio 4- composite microsphere

  12. The chemistry of hydrothermal magnetite: a review

    Science.gov (United States)

    Nadoll, Patrick; Angerer, Thomas; Mauk, Jeffrey L.; French, David; Walshe, John

    2014-01-01

    Magnetite (Fe3O4) is a well-recognized petrogenetic indicator and is a common accessory mineral in many ore deposits and their host rocks. Recent years have seen an increased interest in the use of hydrothermal magnetite for provenance studies and as a pathfinder for mineral exploration. A number of studies have investigated how specific formation conditions are reflected in the composition of the respective magnetite. Two fundamental questions underlie these efforts — (i) How can the composition of igneous and, more importantly, hydrothermal magnetite be used to discriminate mineralized areas from barren host rocks, and (ii) how can this assist exploration geologists to target ore deposits at greater and greater distances from the main mineralization? Similar to igneous magnetite, the most important factors that govern compositional variations in hydrothermal magnetite are (A) temperature, (B) fluid composition — element availability, (C) oxygen and sulfur fugacity, (D) silicate and sulfide activity, (E) host rock buffering, (F) re-equilibration processes, and (G) intrinsic crystallographic controls such as ionic radius and charge balance. We discuss how specific formation conditions are reflected in the composition of magnetite and review studies that investigate the chemistry of hydrothermal and igneous magnetite from various mineral deposits and their host rocks. Furthermore, we discuss the redox-related alteration of magnetite (martitization and mushketovitization) and mineral inclusions in magnetite and their effect on chemical analyses. Our database includes published and previously unpublished magnetite minor and trace element data for magnetite from (1) banded iron formations (BIF) and related high-grade iron ore deposits in Western Australia, India, and Brazil, (2) Ag–Pb–Zn veins of the Coeur d'Alene district, United States, (3) porphyry Cu–(Au)–(Mo) deposits and associated (4) calcic and magnesian skarn deposits in the southwestern United

  13. Controlled hydrothermal synthesis of BiO{sub x}Cl{sub y}/BiO{sub m}I{sub n} composites exhibiting visible-light photocatalytic degradation of crystal violet

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Yu-Rou; Lin, Ho-Pan [Department of Science Application and Dissemination, National Taichung University of Education, Taichung 403, Taiwan, ROC (China); Chung, Wen-Hsin [Department of Plant Pathology, National Chung Hsing University, Taichung 402, Taiwan, ROC (China); Dai, Yong-Ming [Department of Science Application and Dissemination, National Taichung University of Education, Taichung 403, Taiwan, ROC (China); Lin, Wan-Yu [Department of Plant Pathology, National Chung Hsing University, Taichung 402, Taiwan, ROC (China); Chen, Chiing-Chang, E-mail: ccchen@ms3.ntcu.edu.tw [Department of Science Application and Dissemination, National Taichung University of Education, Taichung 403, Taiwan, ROC (China)

    2015-02-11

    Highlights: • This is the first report on a series of BiO{sub x}Cl{sub y}/BiO{sub m}I{sub n} heterojunctions. • The BiO{sub x}Cl{sub y}/BiO{sub m}I{sub n} composition was controlled by adjusting the growth parameters. • The BiO{sub x}Cl{sub y}/BiO{sub m}I{sub n} were indirect semiconductors with a 1.78–2.95-eV bandgap. • The new photocatalysts removed CV at a much faster rate than TiO{sub 2}. • Mechanisms were determined by separating the intermediates using HPLC-MS. - Abstract: A series of BiO{sub x}Cl{sub y}/BiO{sub m}I{sub n} composites were prepared using autoclave hydrothermal methods. The composition and morphologies of the BiO{sub x}Cl{sub y}/BiO{sub m}I{sub n} composites were controlled by adjusting the experimental conditions: the reaction pH value, temperature, and KCl/KI molar ratio. The products were characterized using X-ray diffraction, scanning electron microscopy-electron dispersive X-ray spectroscopy, UV–vis diffuse reflectance spectroscopy, Brunauer–Emmett–Teller specific surface areas, cathodoluminescence, high-resolution transmission electron microscopy, and high-resolution X-ray photoelectron spectroscopy. The photocatalytic efficiencies of composite powder suspensions were evaluated by monitoring the crystal violet (CV) concentrations. In addition, the quenching effects of various scavengers indicated that the reactive O{sub 2}·{sup −} played a major role, and OH· or h{sup +} played a minor role in CV degradation. The intermediates formed during the decomposition process were isolated, identified, and characterized using high performance liquid chromatography-photodiode array-electrospray ionization-mass spectrometry to elucidate the CV decomposition mechanism.

  14. Hydrothermal pretreatment of coal

    Energy Technology Data Exchange (ETDEWEB)

    Ross, D.S.

    1989-12-21

    We have examined changes in Argonne Premium samples of Wyodak coal following 30 min treatment in liquid water at autogenous pressures at 150{degrees}, 250{degrees}, and 350{degrees}C. In most runs the coal was initially dried at 60{degrees}C/1 torr/20 hr. The changes were monitored by pyrolysis field ionization mass spectrometry (py-FIMS) operating at 2.5{degrees}C/min from ambient to 500{degrees}C. We recorded the volatility patterns of the coal tars evolved over that temperature range, and in all cases the tar yields were 25%--30% of the starting coal on mass basis. There was essentially no change after the 150{degrees}C treatment. Small increases in volatility were seen following the 250{degrees}C treatment, but major effects were seen in the 350{degrees} work. The tar quantity remained unchanged; however, the volatility increased so the temperature of half volatility for the as-received coal of 400{degrees}C was reduced to 340{degrees}C. Control runs with no water showed some thermal effect, but the net effect from the presence of liquid water was clearly evident. The composition was unchanged after the 150{degrees} and 250{degrees}C treatments, but the 350{degrees} treatment brought about a 30% loss of oxygen. The change corresponded to loss of the elements of water, although loss of OH'' seemed to fit the analysis data somewhat better. The water loss takes place both in the presence and in the absence of added water, but it is noteworthy that the loss in the hydrothermal runs occurs at p(H{sub 2}O) = 160 atm. We conclude that the process must involve the dehydration solely of chemically bound elements of water, the dehydration of catechol is a specific, likely candidate.

  15. 高水热稳定性加氢脱氧Ni-Mo复合氧化物催化剂的制备%Preparation of Ni-Mo Composite Oxide Catalysts with High Hydrothermal Stability for Hydrodeoxygenation

    Institute of Scientific and Technical Information of China (English)

    任阳阳; 宋运晶; 段艳; 侯凯湖

    2015-01-01

    以动植物油脂为原料加氢脱氧生产生物柴油的关键是开发具有优异加氢脱氧活性和稳定性的新型催化剂.今采用溶胶凝胶法制备了本体型Ni-Mo复合氧化物加氢脱氧催化剂,并对其进行了XRD、BET等表征,以含 20%小桐子油的正辛烷溶液为原料,在连续固定床反应装置上考察了催化剂的活性和水热稳定性.结果表明:溶胶凝胶法可制备出具有优异活性的钼镍复合氧化物催化剂,水热处理后催化剂的比表面积和孔容减小以及形成了部分NiMoO 4新相,前者使催化剂的活性下降,后者使催化剂的活性增加,二者的综合作用使水热处理催化剂的活性下降.提高催化剂的焙烧温度或添加镁铝尖晶石等方法可有效改善催化剂的水热稳定性和调控小桐子油的加氢脱氧反应路径.在330℃、2~5 h?1和310℃、2 h?1条件下,小桐子油在700℃焙烧、水热处理前后的催化剂上的脱氧率均高达99.0%以上.与在水热处理前催化剂上的反应结果相比,小桐子油在水热处理后催化剂上的脱羧基、脱羰基反应产物增加了15%.%Key issue of biodiesel production technique via the hydrodeoxygenation of animal and vegetable fats is to develop novel catalysts with excellent hydrodeoxygenation(HDO) activity and stability. A kind of unsupported Ni-Mo composite oxide catalysts were prepared by the sol-gel method in this paper, The prepared catalysts were characterized by XRD and BET. Using the solution of 20%(vol) jatropha curcas oil + 80%(vol) n-octane as the feed, the HDO performance and hydrothermal stability of the catalysts were investigated in a continuous flow fixed-bed reactor. The results show that Mo-Ni composite oxide catalysts prepared by sol-gel method could possess higher hydrodeoxygenation activity.The surface area and pore volume of the catalysts decreases and the some NiMoO 4 can be formed after the hydrothermal treatment. The surface area and pore volume

  16. Surfactant-free hydrothermal synthesis of lithium aluminate microbricks and nanorods from aluminium oxide nanoparticles.

    Science.gov (United States)

    Joshi, Upendra A; Chung, Soo Hyun; Lee, Jae Sung

    2005-09-21

    Beta-LiAlO2 microbricks and rectangular nanorods have been successfully synthesized from Al2O3 nanoparticles by a simple hydrothermal process without any surfactant or template, by simply changing the Li/Al molar ratio.

  17. S- and Sr-isotopic compositions in barite-silica chimney from the Franklin Seamount, Woodlark Basin, Papua New Guinea: constraints on genesis and temporal variability of hydrothermal fluid

    Science.gov (United States)

    Ray, Durbar; Banerjee, Ranadip; Balakrishnan, S.; Paropkari, Anil L.; Mukhopadhyay, Subir

    2016-08-01

    Isotopic ratios of strontium and sulfur in six layers across a horizontal section of a hydrothermal barite-silica chimney from Franklin Seamount of western Woodlark Basin have been investigated. Sr-isotopic ratios in barite samples (87Sr/86Sr = 0.70478-0.70493) are less radiogenic than seawater (87Sr/86Sr = 0.70917) indicating that substantial leaching of sub-seafloor magma was involved in the genesis of hydrothermal fluid. The SO2 of magma likely contributed a considerable amount of lighter S-isotope in fluid and responsible for the formation of barite, which is isotopically lighter (δ34S = 19.4-20.5 ‰) than modern seawater (δ34S ~ 21 ‰). The systematic changes in isotopic compositions across the chimney wall suggest temporal changes in the mode of mineral formation during the growth of the chimney. Enrichment of heavy S- and Sr-isotopes (δ34S = 20.58 ‰; 87Sr/86Sr = 0.70493) in the outermost periphery of the chimney indicates that, at the initial stage of chimney development, there was a significant contribution of seawater sulfate during barite mineralization. Thereafter, thickening of chimney wall occurred due to precipitation of fluid carrying more magmatic components relative to seawater. This led to a gradual enrichment of lighter isotopes (δ34S = 20.42-19.48 ‰; 87Sr/86Sr = 0.70491-0.704787) toward the inner portion of the chimney wall. In contrast, the innermost layer surrounding the fluid conduit is characterized by heavier and more radiogenic isotopes (δ34S = 20.3 ‰; 87Sr/86Sr = 0.7049). This suggests there was increasing influence of percolating seawater on the mineral paragenesis at the waning phase of the chimney development.

  18. Characteristics of Hydrothermal Mineralization in Ultraslow Spreading Ridges

    Science.gov (United States)

    Zhou, H.; Yang, Q.; Ji, F.; Dick, H. J.

    2014-12-01

    Hydrothermal activity is a major component of the processes that shape the composition and structure of the ocean crust, providing a major pathway for the exchange of heat and elements between the Earth's crust and oceans, and a locus for intense biological activity on the seafloor and underlying crust. In other hand, the structure and composition of hydrothermal systems are the result of complex interactions between heat sources, fluids, wall rocks, tectonic controls and even biological processes. Ultraslow spreading ridges, including the Southwest Indian Ridge, the Gakkel Ridge, are most remarkable end member in plate-boundary structures (Dick et al., 2003), featured with extensive tectonic amagmatic spreading and frequent exposure of peridotite and gabbro. With intensive surveys in last decades, it is suggested that ultraslow ridges are several times more effective than faster-spreading ridges in sustaining hydrothermal activities. This increased efficiency could attributed to deep mining of heat and even exothermic serpentinisation (Baker et al., 2004). Distinct from in faster spreading ridges, one characteristics of hydrothermal mineralization on seafloor in ultraslow spreading ridges, including the active Dragon Flag hydrothermal field at 49.6 degree of the Southwest Indian Ridge, is abundant and pervasive distribution of lower temperature precipitated minerals ( such as Fe-silica or silica, Mn (Fe) oxides, sepiolite, pyrite, marcasite etc. ) in hydrothermal fields. Structures formed by lower temperature activities in active and dead hydrothermal fields are also obviously. High temperature precipitated minerals such as chalcopyrite etc. are rare or very limited in hydrothermal chimneys. Distribution of diverse low temperature hydrothermal activities is consistence with the deep heating mechanisms and hydrothermal circulations in the complex background of ultraslow spreading tectonics. Meanwhile, deeper and larger mineralization at certain locations along the

  19. Preparation of ZnO nanosheets by a novel microemulsion-based hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Jiang Junying [College of Chemistry and Ecological Engineering, Guangxi University for Nationalities, Nanning 530006 (China); Wenshan Middle School, Weifang 261300 (China); Huang Zaiyin, E-mail: zaiyinhuang2010@163.com [College of Chemistry and Ecological Engineering, Guangxi University for Nationalities, Nanning 530006 (China); Tan Shengwei; Li Yanfen; Wang Guotao; Tan Xuecai [College of Chemistry and Ecological Engineering, Guangxi University for Nationalities, Nanning 530006 (China)

    2012-02-15

    Highlights: Black-Right-Pointing-Pointer We synthesized ZnO nanosheets via a novel hydrothermal method. Black-Right-Pointing-Pointer The ZnO nanosheets exhibited a clearly electrocatalytic response. Black-Right-Pointing-Pointer The ZnO nanosheets exhibited an intense green-yellow luminescence. Black-Right-Pointing-Pointer We discussed the formation mechanism of the prepared ZnO nanosheets. - Abstract: ZnO nanosheets have been successfully synthesized via a novel microemulsion-mediated hydrothermal route at 80 Degree-Sign C for 12 h. The compositions and morphologies of the as-prepared nanosheets were characterized by X-ray power diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and selected-area electron diffraction analysis (SAED). Electrochemical (EA) and photoluminescence analysis (PL) were employed to study their electrochemical behaviors and optical properties. It was found that these ZnO nanosheets had a single crystal hexagonal wurtzite structure with lattice constants of a = 0.3249 nm and c = 0.5205 nm. And they exhibited a clearly electrocatalytic response, indicating that the ZnO nanosheets could accelerate electron transfer of the electrochemical probe. The PL spectrum of ZnO nanosheets exhibited an intense green-yellow luminescence at the wavelength of 569 nm, which can be ascribed to the defects related to oxygen vacancies. The formation mechanism of the nanostructures was also proposed and discussed.

  20. Effects of TiO2 content on the microstructure, mechanical properties and photocatalytic activity of three dimensional TiO2-Graphene composite prepared by hydrothermal reaction

    Science.gov (United States)

    Shi, Xiangru; Chen, Jian; Wang, Wenxiu; Wang, Zengmei; Zhang, Yao; Guo, Xinli

    2016-07-01

    A series of three dimensional (3D) porous TiO2-graphene (TGR) hydrogel samples with different mass ratio of graphene to TiO2 were obtained using a one-step hydrothermal method. Their microstructure, mechanical properties, and photocatalytic activity were investigated. The TGR samples exhibited well defined interconnected 3D porous network microstructure and good mechanical strength. Moreover, the pore size and the compressive strength could be easily adjusted by changing the content of TiO2, showing a decreasing tendency with the increase of the relative content of TiO2. The results of the photodegradation of methylene blue indicated that the photocatalytic activity of the TGR samples can be significantly enhanced, compared to the pure TiO2 nanoparticles. The TGR sample also showed good durability and reusability. The mechanisms resulting in the improvement of photocatalytic activity were investigated with DRS, PL spectra, and adsorption experiment under dark conditions. It was found that adsorption is the dominant factor for the enhanced photocatalytic activity.

  1. Catalytic Hydrothermal Gasification

    Energy Technology Data Exchange (ETDEWEB)

    Elliott, Douglas C.

    2015-05-31

    The term “hydrothermal” used here refers to the processing of biomass in water slurries at elevated temperature and pressure to facilitate the chemical conversion of the organic structures in biomass into useful fuels. The process is meant to provide a means for treating wet biomass materials without drying and to access ionic reaction conditions by maintaining a liquid water processing medium. Typical hydrothermal processing conditions are 523-647K of temperature and operating pressures from 4-22 MPa of pressure. The temperature is sufficient to initiate pyrolytic mechanisms in the biopolymers while the pressure is sufficient to maintain a liquid water processing phase. Hydrothermal gasification is accomplished at the upper end of the process temperature range. It can be considered an extension of the hydrothermal liquefaction mechanisms that begin at the lowest hydrothermal conditions with subsequent decomposition of biopolymer fragments formed in liquefaction to smaller molecules and eventually to gas. Typically, hydrothermal gasification requires an active catalyst to accomplish reasonable rates of gas formation from biomass.

  2. Hydrothermal synthesis of NiCo2O4 nanowires/nitrogen-doped graphene for high-performance supercapacitor

    Science.gov (United States)

    Yu, Mei; Chen, Jianpeng; Ma, Yuxiao; Zhang, Jingdan; Liu, Jianhua; Li, Songmei; An, Junwei

    2014-09-01

    NiCo2O4 nanowires/nitrogen-doped graphene (NCO/NG) composite materials were synthesized by hydrothermal treatment in a water-glycerol mixed solvent and subsequent thermal transformation. The obtained materials were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy and Raman spectroscopy. The electrochemical performance of the composites was evaluated by cyclic voltammetry, galvanostatic charge/discharge and electrochemical impedance spectrum techniques. NiCo2O4 nanowires are densely coated by nitrogen-doped graphene and the composite displays good electrochemical performance. The maximum specific capacitance of NCO/NG is 1273.13 F g-1 at 0.5 A g-1 in 6 M KOH aqueous solution, and it exhibits good capacity retention without noticeable degradation after 3000 cycles at 4 A g-1.

  3. Interactions Between Serpentinization, Hydrothermal Activity and Microbial Community at the Lost City Hydrothermal Field

    Science.gov (United States)

    Delacour, A.; Frueh-Green, G. L.; Bernasconi, S. M.; Schaeffer, P.; Frank, M.; Gutjahr, M.; Kelley, D. S.

    2008-12-01

    Seafloor investigations of slow- and ultraslow-spreading ridges have reported many occurrences of exposed mantle peridotites and gabbroic rocks on the ocean floor. Along the Mid-Atlantic Ridge, these uplifted portions of oceanic crust host high-temperature black smoker-type hydrothermal systems (e.g., Rainbow, Logatchev, Saldanha), and the more distinct low-temperature Lost City Hydrothermal Field (LCHF). Built on a southern terrace of the Atlantis Massif, the LCHF is composed of carbonate-brucite chimneys that vent alkaline and low-temperature (40-90°C) hydrothermal fluids. These fluids are related to serpentinization of mantle peridotites, which together with minor gabbroic intrusions form the basement of the LCHF. Long-lived hydrothermal activity at Lost City led to extensive seawater-rock interaction in the basement rocks, as indicated by seawater-like Sr- and mantle to unradiogenic Nd-isotope compositions of the serpentinites. These high fluid fluxes in the southern part of the massif influenced the conditions of serpentinization and have obliterated the early chemical signatures in the serpentinites, especially those of carbon and sulfur. Compared to reducing conditions commonly formed during the first stages of serpentinization, serpentinization at Lost City is characterized by relatively oxidizing conditions resulting in a predominance of magnetite, the mobilization/dissolution and oxidation of igneous sulfides to secondary pyrite, and the incorporation of seawater sulfate, all leading to high bulk-rock S-isotope compositions. The Lost City hydrothermal fluids contain high concentrations in methane, hydrogen, and low-molecular weight hydrocarbons considered as being produced abiotically. In contrast, organic compounds in the serpentinites are dominated by the occurrences of isoprenoids (pristane, phytane, and squalane), polycyclic compounds (hopanes and steranes), and higher abundances of C16 to C20 n-alkanes indicative of a marine organic input. We

  4. The Lassen hydrothermal system

    Science.gov (United States)

    Ingebritsen, Steven E.; Bergfeld, Deborah; Clor, Laura; Evans, William C.

    2016-01-01

    The active Lassen hydrothermal system includes a central vapor-dominated zone or zones beneath the Lassen highlands underlain by ~240 °C high-chloride waters that discharge at lower elevations. It is the best-exposed and largest hydrothermal system in the Cascade Range, discharging 41 ± 10 kg/s of steam (~115 MW) and 23 ± 2 kg/s of high-chloride waters (~27 MW). The Lassen system accounts for a full 1/3 of the total high-temperature hydrothermal heat discharge in the U.S. Cascades (140/400 MW). Hydrothermal heat discharge of ~140 MW can be supported by crystallization and cooling of silicic magma at a rate of ~2400 km3/Ma, and the ongoing rates of heat and magmatic CO2 discharge are broadly consistent with a petrologic model for basalt-driven magmatic evolution. The clustering of observed seismicity at ~4–5 km depth may define zones of thermal cracking where the hydrothermal system mines heat from near-plastic rock. If so, the combined areal extent of the primary heat-transfer zones is ~5 km2, the average conductive heat flux over that area is >25 W/m2, and the conductive-boundary length system or owe to various geologic events such as the eruption of Lassen Peak at 27 ka, deglaciation beginning ~18 ka, the eruptions of Chaos Crags at 1.1 ka, or the minor 1914–1917 eruption at the summit of Lassen Peak. However, there is a rich record of intermittent hydrothermal measurement over the past several decades and more-frequent measurement 2009–present. These data reveal sensitivity to climate and weather conditions, seasonal variability that owes to interaction with the shallow hydrologic system, and a transient 1.5- to twofold increase in high-chloride discharge in response to an earthquake swarm in mid-November 2014.

  5. Electrophoretic deposition of calcium silicate-reduced graphene oxide composites on titanium substrate

    DEFF Research Database (Denmark)

    Mehrali, Mehdi; Akhiani, Amir Reza; Talebian, Sepehr

    2016-01-01

    silicate-reduced graphene oxide (CS-rGO) composites were synthesized, using an in situ hydrothermal method. CS nanowires were uniformly decorated on the rGO, with an appropriate interfacial bonding. The CS-rGO composites behaved like hybrid composites when deposited on a titanium substrate by cathodic......Calcium silicate (CS)/graphene coatings have been used to improve the biological and mechanical fixation of metallic prosthesis. Among the extraordinary features of graphene is its very high mechanical strength, which makes it an attractive nanoreinforcement material for composites. Calcium...

  6. CoS-Graphene Composite Counter Electrode for High Performance Dye-Sensitized Solar Cell.

    Science.gov (United States)

    Wang, Fen; Wu, Congcong; Tan, Yuan; Jin, Tetsuro; Chi, Bo; Pu, Jian; Jian, Li

    2015-02-01

    CoS-graphene composite counter electrode for dye-sensitized solar cell (DSSC) was prepared by coating hydrothermal synthesized CoS with graphene onto the FTO conductive glass. SEM shows that CoS particles are uniformly dispersed in the graphene. The result confirms that the prepared composite counter electrode is of highly electrocatalytic activity towards iodine reduction, which is even better than Pt electrode. And cyclic voltammetry measurement also shows that the composite counter electrode has good stability after 100 scan cycles. DSSC with CoS-graphene as composite counter electrode achieves a maximum power conversion efficiency of 6.31%, which is better than Pt electrode.

  7. Complexing and hydrothermal ore deposition

    CERN Document Server

    Helgeson, Harold C

    1964-01-01

    Complexing and Hydrothermal Ore Deposition provides a synthesis of fact, theory, and interpretative speculation on hydrothermal ore-forming solutions. This book summarizes information and theory of the internal chemistry of aqueous electrolyte solutions accumulated in previous years. The scope of the discussion is limited to those aspects of particular interest to the geologist working on the problem of hydrothermal ore genesis. Wherever feasible, fundamental principles are reviewed. Portions of this text are devoted to calculations of specific hydrothermal equilibriums in multicompone

  8. Selective synthesis and growth mechanism of CeVO4 nanoparticals via hydrothermal method

    Institute of Scientific and Technical Information of China (English)

    LIU Fengzhen; SHAO Xin; YIN Yibin; ZHAO Limin; SUN Qiaozhen; SHAO Zhuwei; LIU Xuehua; MENG Xianhua

    2011-01-01

    Selective-controlled structure and shape of CeVO4 nanocrystals were successfully synthesized via a hydrothermal method from electron microscopy (FESEM) and energy dispersive spectroscopy (EDS). The influence of hydrothermal temperature, precursor solution concentration on the crystal and morphology of products were further studied. The results showed that the as-synthesized products exhibited pure single-crystal CeVO4 nanoparticles with tetragonal structure. The hydrothermal temperature and precursor solution concentration had important effects on the formation of CeVO4 nanoparticles. Furthermore, the growth mechanism of CeVO4 nanoparticles was explained with Ostwald ripening mechanism.

  9. Synthesis of indium oxide cubic crystals by modified hydrothermal route for application in room temperature flexible ethanol sensors

    Energy Technology Data Exchange (ETDEWEB)

    Seetha, M., E-mail: seetha.phy@gmail.com [Department of Physics, SRM University, Kattankulathur, Kancheepuram Dt 603 203 (India); Meena, P. [Department of Physics, PSGR Krishnammal College for Women, Coimbatore 641 046 (India); Mangalaraj, D., E-mail: dmraj800@yahoo.com [DRDO-BU Centre for Life Sciences, Bharathiar University Campus, Coimbatore (India); Department of Nanoscience and Technology, Bharathiar University, Coimbatore 641 014 (India); Masuda, Yoshitake [National Institute of Advanced Industrial Science and Technology (AIST), Nagoya 463-8560 (Japan); Senthil, K. [School of Advanced Materials Science and Engineering, Sungkyunkwan University (Suwon Campus), Cheoncheon-dong 300, Jangan-gu, Suwon 440-746 (Korea, Republic of)

    2012-03-15

    Highlights: Black-Right-Pointing-Pointer For the first time HMT is used in the preparation of indium oxide. Black-Right-Pointing-Pointer HMT itself acts as base for the precursor and results in cubic indium hydroxide. Black-Right-Pointing-Pointer Modified hydrothermal route used for the preparation of cubic indium oxide crystals. Black-Right-Pointing-Pointer As a new approach a composite film synthesized with prepared indium oxide. Black-Right-Pointing-Pointer Film showed good response to ethanol vapours with quick response and recovery times. - Abstract: Indium oxide cubic crystals were prepared by using hexamethylenetetramine and indium chloride without the addition of any structure directing agents. The chemical route followed in the present work was a modified hydrothermal synthesis. The average crystallite size of the prepared cubes was found to be 40 nm. A blue emission at 418 nm was observed at room temperature when the sample was excited with a 380 nm Xenon lamp. This emission due to oxygen vacancies made the material suitable for gas sensing applications. The synthesized material was made as a composite film with polyvinyl alcohol which was more flexible than the films prepared on glass substrates. This flexible film was used as a sensing element and tested with ethanol vapours at room temperature. The film showed fast response as well as recovery to ethanol vapours with a sensor response of about 1.4 for 100 ppm of the gas.

  10. Hydrothermal conversion of biomass

    NARCIS (Netherlands)

    Knezevic, Dragan

    2009-01-01

    This thesis presents research of hydrothermal conversion of biomass (HTC). In this process, hot compressed water (subcritical water) is used as the reaction medium. Therefore this technique is suitable for conversion of wet biomass/ waste streams. By working at high pressures, the evaporation of wat

  11. Hydrothermal Reactivity of Amines

    Science.gov (United States)

    Robinson, K.; Shock, E.; Hartnett, H. E.; Williams, L. B.; Gould, I.

    2013-12-01

    The reactivity of aqueous amines depends on temperature, pH, and redox state [1], all of which are highly variable in hydrothermal systems. Temperature and pH affect the ratio of protonated to unprotonated amines (R-NH2 + H+ = R-NH3+), which act as nucleophiles and electrophiles, respectively. We hypothesize that this dual nature can explain the pH dependence of reaction rates, and predict that rates will approach a maximum at pH = pKa where the ratio of protonated and unprotonated amines approaches one and the two compounds are poised to react with one another. Higher temperatures in hydrothermal systems allow for more rapid reaction rates, readily reversible reactions, and unique carbon-nitrogen chemistry in which water acts as a reagent in addition to being the solvent. In this study, aqueous benzylamine was used as a model compound to explore the reaction mechanisms, kinetics, and equilibria of amines under hydrothermal conditions. Experiments were carried out in anoxic silica glass tubes at 250°C (Psat) using phosphate-buffered solutions to observe changes in reaction rates and product distributions as a function of pH. The rate of decomposition of benzylamine was much faster at pH 4 than at pH 9, consistent with the prediction that benzylamine acts as both nucleophile and an electrophile, and our estimate that the pKa of benzylamine is ~5 at 250°C and Psat. Accordingly, dibenzylamine is the primary product of the reaction of two benzylamine molecules, and this reaction is readily reversible under hydrothermal conditions. Extremely acidic or basic pH can be used to suppress dibenzylamine production, which also suppresses the formation of all other major products, including toluene, benzyl alcohol, dibenzylimine, and tribenzylamine. This suggests that dibenzylamine is the lone primary product that then itself reacts as a precursor to produce the above compounds. Analog experiments performed with ring-substituted benzylamine derivatives and chiral

  12. Synthesis of nanostructured and microstructured ZnO and Zn(OH)2 on activated carbon cloth by hydrothermal and microwave-assisted chemical bath deposition methods

    Science.gov (United States)

    Mosayebi, Elham; Azizian, Saeid; Hajian, Ali

    2015-05-01

    Nanostructured and microstructured ZnO and Zn(OH)2 loaded on activated carbon cloth were synthesized by microwave-assisted chemical bath deposition and hydrothermal methods. By hydrothermal method the deposited sample on carbon fiber is pure ZnO with dandelion-like nanostructures. By microwave-assisted chemical bath method the structure and composition of deposited sample depends on solution pH. At pH = 9.8 the deposited sample on carbon fiber is pure ZnO with flower-like microstructure; but at pH = 10.8 the sample is a mixture of ZnO and Zn(OH)2 with flower-like and rhombic microstructures, respectively. The mechanism of crystal grow by microwave-assisted chemical bath method was investigated by SEM method at both pH.

  13. Hydrothermal treatment of sorption materials. Implications on adsorption heat pumps

    Energy Technology Data Exchange (ETDEWEB)

    Henninger, S.K.; Mueller, S.; Ratzsch, K.F.; Schossig, P.; Henning, H.M. [Fraunhofer-Institut fuer Solare Energiesysteme (ISE), Freiburg im Breisgau (Germany). Dept. of Thermal Systems and Buildings; Munz, G. [PSE AG, Freiburg (Germany)

    2010-07-01

    Material stability of adsorbents for thermally driven systems like heat storage and heat transformation plays a key role. In particular high power-density applications like adsorption heat pumps and chillers in combination with recently developed adsorption materials lead to a significant increased number of cycles over the lifetime (<100'000) making cycle stability crucial. With regard to current developments on composite structures improving the heat and mass transfer, additional stability analysis like thermo-mechanical properties are now getting into focus. This contribution gives a broad overview on the stability of current available sorption materials like silica gels and zeolites, recently developed (silica-) aluminophosphates (AIPO/SAPO) and most novel synthesized metal organic framework (MOF) materials under hydrothermal treatment. The results give a first indication on the suitability of these materials for the use in heat storage, thermally driven sorption heat pumps and cooling machines. Pure powders as well as composites have been analysed under continuous cycling conditions. Whereas the stability of powders and granules have been analysed in-situ by thermogravimetric cycle measurements, a cycling-test rig has been developed in order to realise a lifetime stress of composites consisting of active sorption material and a support structure. The need for a first stage short-cycle analysis is demonstrated impressively by the dramatic loss of more than 50% in sorption capacity of a SAPO-34 sample within the first 10 cycles. Several composite samples have passed a treatment of 30'000 cycles or more and show continuous degradation effects leading to a reduction in sorption capacity of 20% compared to the initial value. (orig.)

  14. One-pot facile synthesis of CuS/graphene composite as anode materials for lithium ion batteries

    Science.gov (United States)

    Tao, Hua-Chao; Yang, Xue-Lin; Zhang, Lu-Lu; Ni, Shi-Bing

    2014-11-01

    CuS/graphene composite has been synthesized by the one-pot hydrothermal method using thiourea as the sulfur source and reducing agent. The formation of CuS nanoparticles and the reduction of graphene oxide occur simultaneously during the hydrothermal process, which enables a uniform dispersion of CuS nanoparticles on the graphene nanosheets. The electrochemical performance of CuS/graphene composite was studied as anode materials for lithium ion batteries. The obtained CuS/graphene composite exhibits a relative high reversible capacity and good cycling stability. The good electrochemical performance of CuS/graphene composite can be attributed to graphene, which improves the electronic conductivity of composite and enhances the interfacial stability of electrode and electrolyte.

  15. Decoration of ZnO Nanorods with Coral Reefs like NiO Nanostructures by the Hydrothermal Growth Method and Their Luminescence Study

    Directory of Open Access Journals (Sweden)

    Mazhar Ali Abbasi

    2014-01-01

    Full Text Available Composite nanostructures of coral reefs like p-type NiO/n-type ZnO were synthesized on fluorine-doped tin oxide glass substrates by hydrothermal growth. Structural characterization was performed by field emission scanning electron microscopy, high-resolution transmission electron microscopy, and X-ray diffraction techniques. This investigation shows that the adopted synthesis leads to high crystalline quality nanostructures. The morphological study shows that the coral reefs like nanostructures are densely packed on the ZnO nanorods. Cathodoluminescence (CL spectra for the synthesized composite nanostructures are dominated mainly by a broad interstitial defect related luminescence centered at ~630 nm. Spatially resolved CL images reveal that the luminescence of the decorated ZnO nanostructures is enhanced by the presence of the NiO.

  16. Acetylene Black/Sulfur Composites Synthesized by a Solution Evaporation Concentration Crystallization Method and Their Electrochemical Properties for Li/S Batteries

    Directory of Open Access Journals (Sweden)

    Zhigao Yang

    2013-07-01

    Full Text Available A novel technique to prepare carbon/sulfur composites as cathode materials for Li/S batteries is proposed, which we call the ‘solution evaporation concentration crystallization’ method. Three composites with different S loadings were prepared, subject to two different solvent evaporation rates from acetylene black (AB/sulfur in carbon disulfide solutions. X-ray diffraction, environmental scanning electron microscopy, transmission electron microscopy, and Brunauer-Emmett-Teller measurements all show that the porous AB structure is well-filled with S. Composites prepared at a lower solvent evaporation rate with 50 wt % S content, had good electrochemical properties, with 1609.67 mAh g−1 after 100 cycles. Composites with better dispersibility at a low solvent evaporation rate can effectively prevent polysulfide from dissolving in the electrolyte, and serve to stabilize the structure of the S cathode during the charge-discharge process.

  17. Layered nickel sulfide-reduced graphene oxide composites synthesized via microwave-assisted method as high performance anode materials of sodium-ion batteries

    Science.gov (United States)

    Qin, Wei; Chen, Taiqiang; Lu, Ting; Chua, Daniel H. C.; Pan, Likun

    2016-01-01

    Layered nickel sulfide (NS)-reduced graphene oxide (RGO) composites are prepared via a simple microwave-assisted method and subsequent annealing in N2/H2 atmosphere. A detailed array of characterization tools are used to study their morphology, structure and electrochemical performance. It was found that these composites exhibit significantly improved sodium-ion storage ability as compared with pure NS under galvanostatic cycling at a specific current of 100 mA g-1 in a potential limitation of 0.005-3.0 V. Furthermore, the composite with the RGO content of 35 wt.% achieves a high maximum reversible specific capacity of about 391.6 mAh g-1 at a specific current of 100 mA g-1 after 50 cycles. These results prove that NS-RGO composites are highly promising when applied directly as anode materials in sodium-ion batteries.

  18. Ultrafast Nanocrystalline-TiO2 (B)/Carbon Nanotube Hyperdispersion Prepared via Combined Ultracentrifugation and Hydrothermal Treatments for Hybrid Supercapacitors.

    Science.gov (United States)

    Naoi, Katsuhiko; Kurita, Takayuki; Abe, Masayuki; Furuhashi, Takumi; Abe, Yuta; Okazaki, Keita; Miyamoto, Junichi; Iwama, Etsuro; Aoyagi, Shintaro; Naoi, Wako; Simon, Patrice

    2016-08-01

    Anisotropically grown (b-axis short) single-nano TiO2 (B), uniformly hyper-dispersed on the surface of multiwalled carbon nanotubes (MWCNT), was successfully synthesized via an in situ ultracentrifugation (UC) process coupled with a follow-up hydrothermal treatment. The uc-TiO2 (B)/MWCNT composite materials enable ultrafast Li(+) intercalation especially along the b-axis, resulting in a capacity of 235 mA h g(-1) per TiO2 (B) even at 300C (1C = 335 mA g(-1) ).

  19. Micro-structural and compositional variations of hydrothermal epidote-group minerals from a peralkaline granite, Corupá Pluton, Graciosa Province, South Brazil, and their petrological implications

    Directory of Open Access Journals (Sweden)

    Silvio R.F. Vlach

    2012-06-01

    Full Text Available Epidote-group minerals, together with albite, quartz, fluorite, Al-poor and Fe-rich phyllosilicates, zircon, and minor oxides and sulphides, are typical hydrothermal phases in peralkaline alkali-feldspar granites from the Corupá Pluton, Graciosa Province, South Brazil. The epidote-group minerals occur as single crystals and as aggregates filling in rock interstices and miarolitic cavities. They display complex recurrent zoning patterns with an internal zone of ferriallanite-(Ce, followed by allanite-(Ce, then epidote-ferriepidote, and an external zone with allanite-(Ce, with sharp limits, as shown in BSE and X-ray images. REE patterns show decreasing fractionation degrees of LREE over HREE from ferriallanite to epidote. The most external allanite is enriched in MREE. LA-ICP-MS data indicate that ferriallanite is enriched (>10-fold in Ti, Sr and Ga, and depleted in Mg, Rb, Th and Zr relative to the host granite. Allanite has lower Ga and Mn and higher Zr, Nb and U contents as compared to ferriallanite, while epidote is enriched in Sr, U and depleted in Pb, Zr, Hf, Ti and Ga. The formation of these minerals is related to the variable concentrations of HFSE, Ca, Al, Fe and F in fluids remaining from magmatic crystallization, in an oxidizing environment, close to the HM buffer. L-MREE were in part released by the alteration of chevkinite, their main primary repository in the host rocks.Minerais do grupo do epidoto, com albita, quartzo, fluorita, filossilicatos pobres em Al e ricos em Fe, zircão e quantidades menores de óxidos e sulfetos são fases hidrotermais típicas em álcali-feldpato granitos peralcalinos do Pluton Corupá, Província Graciosa, Sul do Brasil. Os minerais do grupo do epidoto ocorrem como cristais individuais ou agregados que preenchem interstícios e cavidades miarolíticas na rocha. Mostram zonamento complexo, recorrente, descrito por uma zona interna de ferriallanita-(Ce, seguida por allanita-(Ce, epidoto-ferriepidoto e uma

  20. Synthesis and highly visible-induced photocatalytic activity of CNT-CdSe composite for methylene blue solution

    Directory of Open Access Journals (Sweden)

    Chen Ming-Liang

    2011-01-01

    Full Text Available Abstract Carbon nanotube-cadmium selenide (CNT-CdSe composite was synthesized by a facile hydrothermal method derived from multi-walled carbon nanotubes as a stating material. The as-prepared products were characterized by X-ray diffraction, scanning electron microscopy with energy dispersive X-ray analysis, transmission electron microscopy (TEM, and UV-vis diffuse reflectance spectrophotometer. The as-synthesized CNT-CdSe composite efficiently catalyzed the photodegradation of methylene blue in aqueous solutions under visible-light irradiation, exhibiting higher photocatalytic activity.

  1. Hydrothermal synthesis of zeolites from natural stellerite

    Institute of Scientific and Technical Information of China (English)

    李酽; 汪信; 董元彩; 朱俊武

    2002-01-01

    Y and P zeolites were synthesized hydrothermally from natural stellerite under different conditions and were characterized via XRD and FT-IR.The results show that the higher crystallinity of Y zeolite can be obtained in hydrothermal system with low alkalinity,low Ca2+/Na+ ratio,and high SiO2/Al2O3 ratio.The lattice space of the samples decreases as crystallization time increases.P Zeolite is prompted under condition of higher alkalinity and higher Ca2+/Na+ ratio.The intensity and number of bands in the range of 400 cm-1~900 cm-1 increases with reaction time.Bands at 680 cm-1,760 cm-1 and 860 cm-1 corresponding to Y zeolite appear during the crystallization stage.Most of these bands shift to higher wavenumbers when SiO2/Al2O3 ratio increases generally.In the hydrothermal system with reverse condition above,bands at 600 cm-1,420 cm-1~470 cm-1 hardly change as the crystallization time increases and the main crystal phase of P zeolite is obtained.

  2. Secondary Crystal Growth on a Cracked Hydrotalcite-Based Film Synthesized by the Sol-Gel Method.

    Science.gov (United States)

    Lee, Wooyoung; Lee, Chan Hyun; Lee, Ki Bong

    2016-05-02

    The sol-gel synthesis method is an attractive technology for the fabrication of ceramic films due to its preparation simplicity and ease of varying the metal composition. However, this technique presents some limitations in relation to the film thickness. Notably, when the film thickness exceeds the critical limit, large tensile stresses occur, resulting in a cracked morphology. In this study, a secondary crystal growth method was introduced as a post-treatment process for Mg/Al hydrotalcite-based films synthesized by the sol-gel method, which typically present a cracked morphology. The cracked hydrotalcite-based film was hydrothermally treated for the secondary growth of hydrotalcite crystals. In the resulting film, hydrotalcite grew with a vertical orientation, and the gaps formed during the sol-gel synthesis were filled with hydrotalcite after the crystal growth. The secondary crystal growth method provides a new solution for cracked ceramic films synthesized by the sol-gel method.

  3. Magnetic and Dielectric Investigations of Mn-Doped Ba Hexaferrite Nanoparticles by Hydrothermal Approach

    Science.gov (United States)

    Adeela, N.; Khan, U.; Iqbal, M.; Riaz, S.; Ali, H.; Maaz, K.; Naseem, S.

    2016-11-01

    A hydrothermal method followed by heat treatment was used to synthesize Mn-substituted Ba2Co2- x Mn x Fe12O22 nanoparticles with a nominal chemical composition of 0 ≤ x magnetic measurements. It was found that the sample at x = 0.9 is of particular interest due to its large coercivity and anisotropy. Later on, for x = 0.9, temperature-dependent magnetic analyses including hysteresis loops, zero-field-cooled, and field-cooled at a particular field of 100 Oe were performed. The decreasing trend in saturation magnetization with increase in temperature was estimated. On the other hand, first an increase and then decrease in coercivity values were observed. These loops also revealed dependence of coercivity on magneto-crystalline anisotropy and average crystallite size of nanoparticles. Dielectric measurements at x = 0.9 make it suitable for high frequency applications.

  4. Synthesis of highly magnetic graphite-encapsulated FeCo nanoparticles using a hydrothermal process

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Seung Jae; Park, Joung Kyu [Center for Nano-Bio Fusion Research, Korea Research Institute of Chemical Technology, Daejeon, 305-600 (Korea, Republic of); Cho, Jee-Hyun; Lee, Chulhyun; Cho, Janggeun [Division of Magnetic Resonance Research, Korea Basic Science Institute, Ochang, 363-883 (Korea, Republic of); Kim, Yong-Rok, E-mail: parkjk@krict.re.kr [Department of Chemistry, Yonsei University, Seoul, 120-749 (Korea, Republic of)

    2011-09-16

    The graphite encapsulation of metal alloy magnetic nanoparticles has attracted attention for biological applications because of the high magnetization of the encapsulated particles. However, most of the synthetic methods have limitations in terms of scalability and economics because of the demanding synthetic conditions and low yields. Here, we show that well controlled graphite-encapsulated FeCo core-shell nanoparticles can be synthesized by a hydrothermal method, simply by mixing Fe/Co with sucrose as a carbon source. Various Fe/Co metal ratios were used to determine the compositional dependence of the saturation magnetization and relaxivity coefficient. Transmission electron microscopy indicated that the particle sizes were 7 nm. In order to test the capability of graphite-encapsulated FeCo nanoparticles as magnetic resonance imaging (MRI) contrast agents, these nanoparticles were solubilized in water by the nonspecific physical adsorption of sodium dodecylbenzene sulfonate.

  5. Decorating multiwalled carbon nanotubes with zinc oxide nano-crystallines through hydrothermal growth process

    Institute of Scientific and Technical Information of China (English)

    LI ChenSha; QIAO YingJie; LI YuMing

    2012-01-01

    Multiwalled-carbon nanotubes coated with nano-crystalline zinc oxide (ZnO) was prepared by in situ growth of nano zinc oxide on the surfaces of carbon nanotubes through hydrothermal method.X-ray diffraction,transmission electron microscopy and scanning electron microscopy analysis techniques were used to characterize the samples.It was observed that a layer of nano-crystalline ZnO with the wurtzite hexagonal crystal structure was uniformly coated on the nanotube surfaces with good adhesion,which resulted in the formation of a novel ZnO-nanotube nano composite.In this work,the carbon nanotubes decorated by metal oxide nanoparticles were synthesized by a simple chemical-solution route which is suitable for the large-scale production with low cost.

  6. Synthesis and Characterization of Aluminum Doped Zinc Oxide Nanostructures via Hydrothermal Route

    Directory of Open Access Journals (Sweden)

    A. Alkahlout

    2014-01-01

    Full Text Available Stable crystalline aluminum doped zinc oxide (AZO nanopowders were synthesized using hydrothermal treatment processing. Three different aluminum precursors have been used. The Al-precursors were found to affect the morphology of the obtained nanopowders. AZO nanoparticles based on zinc acetate and aluminum nitrate have been prepared with different Al/Zn molar ratios. XRD investigations revealed that all the obtained powders have single phase zincite structure with purity of about 99%. The effect of aluminum doping ratio in AZO nanoparticles (based on Al-nitrate precursor on structure, phase composition, and particle size has been investigated. The incorporation of Al in ZnO was confirmed by UV-Vis spectroscopy revealing a blue shift due to Burstein-Moss effect.

  7. The influence of Ca-Mg-Al hydrotalcite synthesized from brine water on thermal and mechanical properties of HTlc-EVA composite

    Science.gov (United States)

    Karina, Wiwiek; Heraldy, Eddy; Pramono, Edi; Heriyanto, Astuti, Shanti

    2016-02-01

    Ca-Mg-Al hydrotalcite-like compound (Ca-Mg-Al HTlc) was prepared by co-precipitation method using brine water that is well known as the desalination process waste water. The structure of Ca-Mg-Al HTlc was determined by X-Ray Diffraction (XRD) and Fourier Transform Infrared (FTIR) analysis. Ca-Mg-Al HTlc was studied as a non-halogenated filler in ethylene vinyl acetate (EVA) matrix. Composites with different filler concentrations were prepared to evaluate the influence of Ca-Mg-Al HTlc on thermal and mechanical properties of EVA.The presence of Ca-Mg-Al HTlc in the composite has been confirmed by FTIR analysis. Thermal properties of composites show significant reduction of degradation temperature as well as the loading of HTlc in EVA. However, the total enthalpies combustion of composites with 1% and 5% HTlc loadings higher compared to neat EVA. Further, mechanical properties were determined by tensile test. The result shows that tensile strength and elongation at break of composites decrease relatively by Ca-Mg-Al HTlc addition.

  8. The influence of Ca-Mg-Al hydrotalcite synthesized from brine water on thermal and mechanical properties of HTlc-EVA composite

    Energy Technology Data Exchange (ETDEWEB)

    Karina, Wiwiek, E-mail: wiekarina@gmail.com; Heraldy, Eddy, E-mail: eheraldy@gmail.com; Pramono, Edi; Heriyanto,; Astuti, Shanti [Department of Chemistry, Faculty of Mathematics and Natural Sciences, Sebelas Maret University Jl. Ir. Sutami 36A, Kentingan, Surakarta 57126 (Indonesia)

    2016-02-08

    Ca-Mg-Al hydrotalcite-like compound (Ca-Mg-Al HTlc) was prepared by co-precipitation method using brine water that is well known as the desalination process waste water. The structure of Ca-Mg-Al HTlc was determined by X-Ray Diffraction (XRD) and Fourier Transform Infrared (FTIR) analysis. Ca-Mg-Al HTlc was studied as a non-halogenated filler in ethylene vinyl acetate (EVA) matrix. Composites with different filler concentrations were prepared to evaluate the influence of Ca-Mg-Al HTlc on thermal and mechanical properties of EVA.The presence of Ca-Mg-Al HTlc in the composite has been confirmed by FTIR analysis. Thermal properties of composites show significant reduction of degradation temperature as well as the loading of HTlc in EVA. However, the total enthalpies combustion of composites with 1% and 5% HTlc loadings higher compared to neat EVA. Further, mechanical properties were determined by tensile test. The result shows that tensile strength and elongation at break of composites decrease relatively by Ca-Mg-Al HTlc addition.

  9. On the Novel Biaxial Strain Relaxation Mechanism in Epitaxial Composition Graded La1−xSrxMnO3 Thin Film Synthesized by RF Magnetron Sputtering

    Directory of Open Access Journals (Sweden)

    Yishu Wang

    2015-11-01

    Full Text Available We report on a novel method to fabricate composition gradient, epitaxial La1−xSrxMnO3 thin films with the objective to alleviate biaxial film strain. In this work, epitaxial, composition gradient La1−xSrxMnO3, and pure LaMnO3 and La0.67Sr0.33MnO3 thin films were deposited by radio frequency (RF magnetron sputtering. The crystalline and epitaxy of all films were first studied by symmetric θ–2θ X-ray diffraction (XRD and low angle XRD experiments. Detailed microstructural characterization across the film thickness was conducted by high-resolution transmission electron microscopy and electron diffraction. Four compositional gradient domains were observed in the La1−xSrxMnO3 film ranging from LaMnO3 rich to La0.67Sr0.33MnO3 at the surface. A continuous reduction in the lattice parameter was observed accompanied by a significant reduction in the out-of-plane strain in the film. Fabrication of the composition gradient La1−xSrxMnO3 thin film was found to be a powerful method to relieve biaxial strain under critical thickness. Besides, the coexistence of domains with a composition variance is opening up various new possibilities of designing new nanoscale structures with unusual cross coupled properties.

  10. Anhydrite precipitation in seafloor hydrothermal systems

    Science.gov (United States)

    Theissen-Krah, Sonja; Rüpke, Lars H.

    2016-04-01

    The composition and metal concentration of hydrothermal fluids venting at the seafloor is strongly temperature-dependent and fluids above 300°C are required to transport metals to the seafloor (Hannington et al. 2010). Ore-forming hydrothermal systems and high temperature vents in general are often associated with faults and fracture zones, i.e. zones of enhanced permeabilities that act as channels for the uprising hydrothermal fluid (Heinrich & Candela, 2014). Previous numerical models (Jupp and Schultz, 2000; Andersen et al. 2015) however have shown that high permeabilities tend to decrease fluid flow temperatures due to mixing with cold seawater and the resulting high fluid fluxes that lead to short residence times of the fluid near the heat source. A possible mechanism to reduce the permeability and thereby to focus high temperature fluid flow are mineral precipitation reactions that clog the pore space. Anhydrite for example precipitates from seawater if it is heated to temperatures above ~150°C or due to mixing of seawater with hydrothermal fluids that usually have high Calcium concentrations. We have implemented anhydrite reactions (precipitation and dissolution) in our finite element numerical models of hydrothermal circulation. The initial results show that the precipitation of anhydrite efficiently alters the permeability field, which affects the hydrothermal flow field as well as the resulting vent temperatures. C. Andersen et al. (2015), Fault geometry and permeability contrast control vent temperatures at the Logatchev 1 hydrothermal field, Mid-Atlantic Ridge, Geology, 43(1), 51-54. M. D. Hannington et al. (2010), Modern Sea-Floor Massive Sulfides and Base Metal Resources: Toward an Estimate of Global Sea-Floor Massive Sulfide Potential, in The Challenge of Finding New Mineral Resources: Global Metallogeny, Innovative Exploration, and New Discoveries, edited by R. J. Goldfarb, E. E. Marsh and T. Monecke, pp. 317-338, Society of Economic Geologists

  11. Hydrothermal liquefaction of biomass

    DEFF Research Database (Denmark)

    Toor, Saqib; Rosendahl, Lasse; Hoffmann, Jessica

    2014-01-01

    Biomass is one of the most abundant sources of renewable energy, and will be an important part of a more sustainable future energy system. In addition to direct combustion, there is growing attention on conversion of biomass into liquid en-ergy carriers. These conversion methods are divided...... into liquid biofuels, with the aim of describing the current status and development challenges of the technology. During the hydrothermal liquefaction process, the biomass macromolecules are first hydrolyzed and/or degraded into smaller molecules. Many of the produced molecules are unstable and reactive...... into biochemical/biotechnical methods and thermochemical methods; such as direct combustion, pyrolysis, gasification, liquefaction etc. This chapter will focus on hydrothermal liquefaction, where high pressures and intermediate temperatures together with the presence of water are used to convert biomass...

  12. Hydrothermal liquefaction of biomass

    DEFF Research Database (Denmark)

    Toor, Saqib; Rosendahl, Lasse; Hoffmann, Jessica

    2014-01-01

    Biomass is one of the most abundant sources of renewable energy, and will be an important part of a more sustainable future energy system. In addition to direct combustion, there is growing attention on conversion of biomass into liquid en-ergy carriers. These conversion methods are divided...... into biochemical/biotechnical methods and thermochemical methods; such as direct combustion, pyrolysis, gasification, liquefaction etc. This chapter will focus on hydrothermal liquefaction, where high pressures and intermediate temperatures together with the presence of water are used to convert biomass...... into liquid biofuels, with the aim of describing the current status and development challenges of the technology. During the hydrothermal liquefaction process, the biomass macromolecules are first hydrolyzed and/or degraded into smaller molecules. Many of the produced molecules are unstable and reactive...

  13. Hydrothermal synthesis and characterizations of Ti substituted Mn-ferrites

    Energy Technology Data Exchange (ETDEWEB)

    Mostafa, Nasser Y., E-mail: nmost69@yahoo.com [Faculty of Science, Taif University, P.O. Box 888 Al-Haweiah, Taif (Saudi Arabia); Chemistry Department, Faculty of Science, Suez Canal University, Ismailia 41522 (Egypt); Hessien, M.M. [Faculty of Science, Taif University, P.O. Box 888 Al-Haweiah, Taif (Saudi Arabia); Advanced materials Division-Central metallurgical R and D Institute (CMRDI), P.O. Box 87 Helwan, Cairo (Egypt); Shaltout, Abdallah A. [Faculty of Science, Taif University, P.O. Box 888 Al-Haweiah, Taif (Saudi Arabia); Spectroscopy Department, Physics Division, National Research Center, El Behooth Str., 12622 Dokki, Cairo (Egypt)

    2012-07-15

    Highlights: Black-Right-Pointing-Pointer Hydrothermal synthesized of well-crystallized Ti-substituted MnFe{sub 2}O{sub 4} nanoparticles at 180 Degree-Sign C without any calcination step. The chemical composition was represented by Mn{sub 1-2x}Ti{sub x}Fe{sub 2}O{sub 4} with x having values 0.0, 0.1, 0.2, 0.3 and 0.4. Black-Right-Pointing-Pointer The change in lattice parameter and saturation magnetization with increasing Ti-substitution was investigated and explained. Black-Right-Pointing-Pointer The change in microstructure due to Ti{sup 4+} ions substitutions was investigated using TEM analysis. - Abstarct: A series of well-crystallized Mn{sub 1-2x}Ti{sub x}Fe{sub 2}O{sub 4} nanoparticles with x values of 0.0, 0.1, 0.2, 0.3 and 0.4 have been synthesized by hydrothermal route at 180 Degree-Sign C in the presence of NaOH as mineralizer. The obtained ferrite samples were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM) and vibrating sample magnetometer (VSM). The XRD analysis showed that pure single phases of cubic ferrites were obtained with x up to 0.2. However, samples with x > 0.2 showed traces of unreacted anatase. The increase in Ti-substitution up to x = 0.2 leads to an increase in the lattice parameter of the prepared ferrites. On the other hand, the increase in Ti-substitution over x = 0.2 leads to a decrease in the lattice parameter. The average crystallite size was in the range of 39-57 nm, where it is increased by increasing the Ti-substitution up to x = 0.3, then decreased for x = 0.4. According to VSM results, the saturation magnetization increased with Ti ion substitution of x = 0.1 and decreased for x > 0.1.

  14. A NOVEL HYDROTHERMAL SYNTHESIS METHOD FOR BARIUM FERRITE

    Institute of Scientific and Technical Information of China (English)

    Kang Li; Hongchen Gu; Qun Wei

    2004-01-01

    In the present work, fine barium ferrite powder has been synthesized through a one-step hydrothermal process in an autoclave at [OH-]/[Cl-] ratio of 2:1 in the temperature range from 180 to 260 ℃ using barium chloride (BaCl2), ferrous chloride (FeCl2) and potassium nitrate (KNO3) as the starting materials. Both particle size and saturation magnetization (Ms) increase with increasing hydrothermal reaction temperature, while the intrinsic coercivity (iHc) peaks at 685 Oe at 230 ℃. Morphology progress from the barium ferrite precursor particles to the barium hexaferrite particles has been monitored with increasing hydrothermal reaction time at 230 ℃ in the autoclave.

  15. Effect of reactive diluent on hydrothermal properties of T700/BMI composites%活性稀释剂对T700/BMI复合材料湿热性能的影响

    Institute of Scientific and Technical Information of China (English)

    金保宏; 王柏臣; 陈平

    2012-01-01

    采用苯乙烯作二烯丙基双酚A(DABPA)改性双马来酰亚胺(BMI)树脂体系的活性稀释,以减小树脂的粘度.为研究苯乙烯的用量对炭纤维(T700)增强改性BMI树脂基复合材料湿热性能的影响,对T700/BMI复合材料的试样在70℃水中进行吸湿实验,并检测其力学性能.结果表明,随苯乙烯用量的增加,试样的吸湿率降低;其拉伸、弯曲和层间剪切等强度保持率也随之增大;但当苯乙烯在基体树脂中的摩尔百分含量超过20%之后,试样的拉伸强度会下降.%Styrene was used as reactive diluent to decrease the viscosity of Bismaleimide( BMI) resin modified by Diallylbisphe-nol A( DABPA). T700/BMI composite materials were prepared as testing samples,which are made up of the carbon fiber( T700)as reinforcing material and modified BMI resin as matrix. In order to investigate the effects of styrene content in matrix on the hydro-thermal properties of the sample,the moisture absorptions were measured for the samples in 70 ℃ water,and their mechanical properties were tested too. The results show that moisture absorption of the sample can be decreased with increasing styrene content, and the higher styrene content is responsible for the higher retentions in tensile,flexure and lamellar shear strengths for the sample. However the tensile strength of sample declines when styrene content exceeds 20% (mol% ) in matrix.

  16. Local structure of the metal-oxygen bond in compositionally homogeneous, nanocrystalline zirconia-ceria solid solutions synthesized by a gel-combustion process

    Energy Technology Data Exchange (ETDEWEB)

    Fabregas, Ismael O [CINSO - Centro de Investigaciones en Solidos, CITEFA-CONICET, J.B. de La Salle 4397 (1603) Villa Martelli, Provincia de Buenos Aires (Argentina); Fuentes, Rodolfo O [CINSO -Centro de Investigaciones en Solidos, CITEFA-CONICET, J.B. de La Salle 4397 (1603) Villa Martelli, Provincia de Buenos Aires (Argentina); Lamas, Diego G [CINSO - Centro de Investigaciones en Solidos, CITEFA-CONICET, J.B. de La Salle 4397 (1603) Villa Martelli, Provincia de Buenos Aires (Argentina); Rapp, MarIa E Fernandez de [CINSO - Centro de Investigaciones en Solidos, CITEFA-CONICET, J.B. de La Salle 4397 (1603) Villa Martelli, Provincia de Buenos Aires (Argentina); Reca, Noemi E Walsoee de [CINSO - C