scholarly journals Quantified abundance of magnetofossils at the Paleocene–Eocene boundary from synchrotron-based transmission X-ray microscopy

2015 ◽  
Vol 112 (41) ◽  
pp. 12598-12603 ◽  
Author(s):  
Huapei Wang ◽  
Jun Wang ◽  
Yu-chen Karen Chen-Wiegart ◽  
Dennis V. Kent
Keyword(s):  
Magnetic Particles ◽  
Strong Field ◽  
Atlantic Coastal Plain ◽  
Magnetic Studies ◽  
Electron Microscopic ◽  
Natural Sediment ◽  
Full Field ◽  
X Ray ◽  
Transmission Electron ◽  
Carbon Isotope Excursion

The Paleocene–Eocene boundary (∼55.8 million years ago) is marked by an abrupt negative carbon isotope excursion (CIE) that coincides with an oxygen isotope decrease interpreted as the Paleocene–Eocene thermal maximum. Biogenic magnetite (Fe3O4) in the form of giant (micron-sized) spearhead-like and spindle-like magnetofossils, as well as nano-sized magnetotactic bacteria magnetosome chains, have been reported in clay-rich sediments in the New Jersey Atlantic Coastal Plain and were thought to account for the distinctive single-domain magnetic properties of these sediments. Uncalibrated strong field magnet extraction techniques have been typically used to provide material for scanning and transmission electron microscopic imaging of these magnetic particles, whose concentration in the natural sediment is thus difficult to quantify. In this study, we use a recently developed ultrahigh-resolution, synchrotron-based, full-field transmission X-ray microscope to study the iron-rich minerals within the clay sediment in their bulk state. We are able to estimate the total magnetization concentration of the giant biogenic magnetofossils to be only ∼10% of whole sediment. Along with previous rock magnetic studies on the CIE clay, we suggest that most of the magnetite in the clay occurs as isolated, near-equidimensional nanoparticles, a suggestion that points to a nonbiogenic origin, such as comet impact plume condensates in what may be very rapidly deposited CIE clays.

scholarly journals Carbon-coated magnetic particles increase tissue temperatures after laser irradiation

2015 ◽  
Vol 08 (05) ◽  
pp. 1550018 ◽  
Author(s):  
Shupeng Liu ◽  
Na Chen ◽  
Fufei Pang ◽  
Zhengyi Chen ◽  
Tingyun Wang
Keyword(s):  
Laser Irradiation ◽  
Magnetic Particles ◽  
Laser Energy ◽  
Thermal Therapy ◽  
Vibrating Sample Magnetometer ◽  
X Ray Diffraction ◽  
X Ray ◽  
Fbg Sensor ◽  
Transmission Electron ◽  
Carbon Coated

Purpose: This work focused on the investigation the hyperthermia performance of the carbon-coated magnetic particles (CCMPs) in laser-induced hyperthermia. Materials and methods: We prepared CCMPs using the organic carbonization method, and then characterized them with transmission electron microscopy (TEM), ultraviolet-visible (UV-Vis) spectrophotometry, vibrating sample magnetometer (VSM) and X-ray diffraction (XRD). In order to evaluate their performance in hyperthermia, the CCMPs were tested in laser-induced thermal therapy (LITT) experiments, in which we employed a fully distributed fiber Bragg grating (FBG) sensor to profile the tissue's dynamic temperature change under laser irradiation in real time. Results: The sizes of prepared CCMPs were about several micrometers, and the LITT results show that the tissue injected with the CCMPs absorbed more laser energy, and its temperature increased faster than the contrast tissue without CCMPs. Conclusions: The CCMPs may be of great help in hyperthermia applications.

Single Variant Orientational Growth of Yba2Cu3O7-x on Vicinal (011) SrTiO3 Substrates.

1995 ◽  
Vol 401 ◽  
Author(s):  
A. L. Vasiliev ◽  
D. S. Linehan ◽  
E. P. Kvam ◽  
L. Hou ◽  
M. W. McElfresh
Keyword(s):  
Second Phase ◽  
Surface Cracks ◽  
Electron Microscopic ◽  
Ybco Films ◽  
Single Crystalline ◽  
X Ray ◽  
Transmission Electron ◽  
Transmission Electron Microscopic

AbstractThe results of a transmission electron microscopic (TEM) and X-ray microanalysis (EDS) study of Yba2Cu3O7-x (YBCO) films grown on vicinal (011) SrTiO3 substrates are presented. The YBCO films tend to be single crystalline grown in single variant orientation with c-axis =;45° from the surface. Cracks, second phase precipitates (CuO and Y2O3), and a few small YBCO grains in other orientations were revealed in the films.

Synthesis of nanometer-sized particles of barium orthotitanate prepared through a modified reverse micellar route: Structural characterization, phase stability and dielectric properties

2004 ◽  
Vol 19 (10) ◽  
pp. 2905-2912 ◽  
Author(s):  
Tokeer Ahmad ◽  
Ashok K. Ganguli
Keyword(s):  
Martensitic Transition ◽  
Line Broadening ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
X Ray ◽  
Transmission Electron ◽  
Transmission Electron Microscopic ◽  
Microscopic Studies ◽  
Size Of Particles ◽  
Reverse Micellar

Nanoparticles of barium orthotitanate (Ba2TiO4) was obtained using microemulsions (avoiding Ba-alkoxide). Powder x-ray diffraction studies of the powder after calcining at 800 °C resulted in a mixture of orthorhombic (70%) and monoclinic (30%) phases. The high-temperature orthorhombic form present at 800 °C was due to the small size of particles obtained by the reverse micellar route. Pure orthorhombic Ba2TiO4 was obtained on further sintering at 1000 °C with lattice parameters a = 6.101(2) Å, b =22.94(1) Å, c = 10.533(2) Å (space group, P21nb). The particle size obtained from x-ray line broadening studies and transmission electron microscopic studies was found to be 40–50 nm for the powder obtained after heating at 800 °C. Sintering at 1000 °C showed increase in grain size up to 150 nm. Our studies corroborate well with the presence of a martensitic transition in Ba2TiO4. The dielectric constant was found to be 40 for Ba2TiO4 (at 100 kHz) for samples sintered at 1000 °C. The dielectric loss obtained was low (0.06) at 100 kHz.

Magnetoelectric and magnetic studies of the Bi1–xCaxFeO3 multiferrioc system

2014 ◽  
Vol 92 (5) ◽  
pp. 389-394 ◽  
Author(s):  
S.F. Mansour ◽  
N.I. Abu-Elsaad ◽  
T.A. Elmosalami
Keyword(s):  
Room Temperature ◽  
Energy Levels ◽  
Resonance Field ◽  
X Ray Diffraction ◽  
Magnetic Studies ◽  
X Ray ◽  
Transmission Electron ◽  
Spin Resonance ◽  
Particle Size And Shape ◽  
Combustion Technique

Bi1–xCaxFeO3 was prepared by the flash autocombustion combustion technique. X-ray diffraction analysis showed a Rhombohedrally distorted hexagonal perovskite structure with space group R3c. The particle size and shape were studied by transmission electron microscope. Magnetization studies at room temperature showed superparamagnetic behavior for the prepared nanoparticles. Magnetoelectric coefficient characterized as magnetic field – induced polarization was investigated. The Lande factor (g), resonance field (Br), relaxation time (τ), and the energy between two adjacent degenerate spin energy levels (ΔE) were estimated from the electron spin resonance spectra.

LASER-INDUCED PHOTOLUMINESCENT STUDIES OF Al-DOPED ZINC OXIDE NANOPARTICLES

2010 ◽  
Vol 09 (05) ◽  
pp. 439-445
Author(s):  
DHIRAJ KUMAR ◽  
SUNIL KUMAR ◽  
H. S. BHATTI
Keyword(s):  
Zinc Oxide ◽  
Zinc Oxide Nanoparticles ◽  
Oxide Nanoparticles ◽  
Nitrogen Laser ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
Time Resolved ◽  
X Ray ◽  
Aluminum Ions ◽  
Transmission Electron

In this paper, addition of aluminum in zinc oxide is incorporated using low-temperature chemical synthesis route. Aluminum ions help in crystallization of zinc oxide nanoparticles. Characterization of the synthesized nanoparticles of zinc oxide has been done using Transmission electron microscope (TEM), and X-ray diffraction (XRD) analysis, Energy-resolved photoluminescence (PL) spectra and Time-resolved laser-induced photoluminescence (TRPL) at room temperature. Transmission electron microscopic observations and X-Ray diffraction studies indicate highly crystalline nature and particle size of the order of 20 nm in ZnO:Al . Time-resolved laser-induced photoluminescence measurements have been done using pulsed nitrogen laser as an excitation source, operated at wavelength 337.1 nm and having high peak output power of 1 MW. The results show that at higher concentrations of Al doping in host ZnO phosphor, emission intensity is more by several orders of magnitude and lifetime shortening indicates that these nanoparticles are more efficient as compared with lower concentrations of dopant.

scholarly journals Synthesis, Characterization, and Photocatalytic Performance of Mesoporous α-Mn2O3 Microspheres Prepared via a Precipitation Route

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Manoj Pudukudy ◽  
Zahira Yaakob
Keyword(s):  
Electron Microscopy ◽  
Uv Light ◽  
Thermal Transformation ◽  
Xrd Analysis ◽  
Structural Deformation ◽  
Blue Dye ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
X Ray ◽  
Transmission Electron

α-Mn2O3 microspheres with high phase purity, crystallinity, and surface area were synthesized by the thermal decomposition of precipitated MnCO3 microspheres without the use of any structure directing agents and tedious reaction conditions. The prepared Mn2O3 microspheres were characterized by Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) and photoluminescence (PL) studies. The complete thermal transformation of MnCO3 to Mn2O3 was clearly shown by the FTIR and XRD analysis. The electron microscopic images clearly confirmed the microsphere-like morphology of the products with some structural deformation for the calcined Mn2O3 sample. The mesoporous texture generated from the interaggregation of subnanoparticles in the microstructures is visibly evident from the TEM and BET studies. Moreover, the Mn2O3 microstructures showed a moderate photocatalytic activity for the degradation of methylene blue dye pollutant under UV light irradiation, using air as the potential oxidizing agent.

REMOVAL OF THE SURFACTANT SURROUNDING Ag NANOCLUSTERS SYNTHESIZED BY NEW THERMAL DECOMPOSITION METHOD

2002 ◽  
Vol 01 (05n06) ◽  
pp. 477-481 ◽  
Author(s):  
LEE DON KEUN ◽  
YOUNG SOO KANG
Keyword(s):  
Thermal Decomposition ◽  
Silver Nanoclusters ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
Sem Images ◽  
X Ray ◽  
Transmission Electron ◽  
Thermo Gravimetric Analyzer ◽  
Ft Ir ◽  
Complex Transmission

Silver nanoclusters have been formed by thermal decomposition of Ag-oleate complex. Transmission electron microscopic (TEM) images of the particles showed two-dimensional assembly of particles with diameter of 10.5 nm. Energy-dispersive X-ray (EDX) spectrum and X-ray diffraction (XRD) peaks of the nanoclusters showed the highly crystalline nature of the silver structures. The decomposition of silver-oleate complex was analyzed by Thermo Gravimetric Analyzer (TGA) and the crystallization process was observed by XRD. The removal of the surfactant surrounding silver nanoclusters was measured by FT-IR and SEM images.

Magnetic Properties and Fabrication of Monodisperse FePd Nanoparticles

2004 ◽  
Vol 818 ◽  
Author(s):  
Yanglong Hou ◽  
Hiroshi Kondoh ◽  
Toshiaki Ohta
Keyword(s):  
Room Temperature ◽  
Iron Pentacarbonyl ◽  
X Ray Diffraction ◽  
Magnetic Studies ◽  
X Ray ◽  
Transmission Electron ◽  
Adamantanecarboxylic Acid ◽  
Palladium Acetylacetonate ◽  
Crystalline Nature ◽  
Quantum Design Squid Magnetometer

AbstractThe combination of 1-adamantanecarboxylic acid and tri-alkylphosphine was applied to produce monodisperse FePd nanoparticles by the polyol reduction of palladium acetylacetonate and thermally decomposition of iron pentacarbonyl. Images of high resolution transmission electron microscopy (TEM) and X-ray diffraction (XRD) data indicate a highly monodisperse and crystalline nature of the FePd nanoparticles. Magnetic studies performed by Quantum Design SQUID magnetometer show that FePd (16nm) nanoparticles are superparamagnetic at room temperature.

Synthesis and characterization of nanoparticles of Ba2EuZrO5.5: A new complex perovskite ceramic oxide

2000 ◽  
Vol 15 (10) ◽  
pp. 2125-2130 ◽  
Author(s):  
R. Jose ◽  
J. James ◽  
Asha M. John ◽  
R. Divakar ◽  
J. Koshy
Keyword(s):  
High Resolution ◽  
Electron Diffraction ◽  
Particle Size Analysis ◽  
Electron Microscopic Investigation ◽  
Perovskite Oxide ◽  
Size Analysis ◽  
Complex Perovskite ◽  
Electron Microscopic ◽  
X Ray ◽  
Transmission Electron

Nanoparticles of barium europium zirconate, a complex perovskite oxide, were synthesized using a modified self-propagating combustion synthesis. The solid combustion products thus obtained were characterized by x-ray and electron diffraction, differential thermal analysis, thermogravimetric analysis, infrared spectroscopy, particle-size analysis, surface area determination, gas adsorption studies, and high-resolution transmission electron microscopy. According to the results of the x-ray and electron diffraction, as-prepared powder showed the single phase of barium europium zirconate (Ba2EuZrO5.5) without another phase and had a complex cubic perovskite (A2BB′O6) structure. The transmission electron microscopic investigation showed a mean grain size of 38 nm with a standard deviation of 12 nm. High-resolution lattice imaging of the nanoparticles indicated the possibility of finer crystallite in the particle having the same orientation. The nanoparticles of Ba2EuZrO5.5 obtained by the present method could be sintered to 97% theoretical density at a relatively low temperature of 1525 °C.

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