Ordered and twinned structure in hexagonal-based potassium tungsten bronze nanosheets

2013 ◽  
Vol 46 (6) ◽  
pp. 1817-1822 ◽  
Author(s):  
Shuangfeng Jia ◽  
Hongqian Sang ◽  
Wenjing Zhang ◽  
Han Zhang ◽  
He Zheng ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Potassium Hydroxide ◽  
Structural Investigation ◽  
Tungsten Bronze ◽  
X Ray Diffraction ◽  
Rotation Symmetry ◽  
X Ray ◽  
Tungsten Foil ◽  
Diffraction Patterns ◽  
Microscopy Techniques

Non-stoichiometric hexagonal-based potassium tungsten bronze (KxWO3) nanosheets were synthesized by oxidizing tungsten foil in potassium hydroxide. The tungsten bronze nanosheets exhibited an ordered monoclinic superstructure as revealed by X-ray diffraction patterns. Further detailed structural investigation by employing electron microscopy techniques showed the coexistence of 120° rotation twinning variants in the superstructure phase, which may result from the rotation symmetry reduction induced by the ordered arrangements of K vacancies during crystal growth.

scholarly journals Green bio-inspired synthesis, characterization and activity of silver nanoparticle forms of Centaurea virgata Lam. and the isolated flavonoid eupatorin

2018 ◽  
Vol 7 (4) ◽  
pp. 372-379 ◽  
Author(s):  
Burcu Sümer Tüzün ◽  
Judit Hohmann ◽  
Bijen Kivcak
Keyword(s):  
Electron Microscopy ◽  
Zeta Potential ◽  
Synthesis Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Characteristic Absorption Band ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Diffraction Patterns ◽  
Isolated Compound

AbstractA green synthesis method of silver nanoparticles (AgNPs) usingCentaurea virgataLam. extract and the isolated compound eupatorin was investigated in this study. Ultraviolet-visible (UV-Vis) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM)/energy-dispersive X-ray (EDX) spectroscopy, thermal gravimetric analysis, X-ray diffraction analysis and zeta potential were used for characterization of AgNPs. The UV-Vis spectrum exhibited a characteristic absorption band at 420 nm for monodisperse nanoparticles. FTIR measurements also proved the formation. X-ray diffraction patterns showed peaks at (110) and (112), which are characteristic for hexagonal crystals and also showed peaks at (111), (200) and (240), which are characteristic for orthorhombic crystals. The TEM images of AgNPs show that the morphology of AgNPs was predominantly spherical. Obtained AgNPs were highly stable according to the zeta potential values. The nitric oxide scavenging activity, which is also related to anticancer activity, of AgNPs was evaluated. It can be concluded thatC. virgataLam. extract and eupatorin can be used as a reducing agent for potential antioxidant AgNP formation.

Synthesis of Carbon Nanosphere at Low Temperatures Based on Bamboo Fiber

2019 ◽  
Vol 966 ◽  
pp. 163-168 ◽  
Author(s):  
Yulia Kirana Lahsmin ◽  
Dahlang Tahir ◽  
Bualkar Abdullah ◽  
Sultan Ilyas ◽  
Inayatul Mutmainna
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Low Temperatures ◽  
Potassium Hydroxide ◽  
Bamboo Fiber ◽  
X Ray Diffraction ◽  
Activation Temperature ◽  
X Ray ◽  
Transmission Electron ◽  
Bamboo Fibers

Carbon Nanosphere (CNs) has been successfully synthesized from bamboo fibers at low temperatures by carbonization and activation. For activation used Potassium Hydroxide (KOH) at temperature 105°C, 155°C, 205°C, 255°C and 305°C. X-Ray Diffraction (XRD) spectra shows hexagonal and amorphous phase and Fourier Transform Infrared (FTIR) spectra shows decrease C-O bond with increasing activation temperature. Transmission Electron Microscopy (TEM) image for activation temperature of 105°C confirmed that sources the formation of Carbon Nanosphere. In this study shows bamboo fiber has a high potential as a carbon nanosphere material.

Influences of Fe2O3 Doping on the Crystallization of SiO2-Al2O3-MgO-K2O-ZrO2-F Glass-Ceramics

2009 ◽  
Vol 79-82 ◽  
pp. 1503-1506 ◽  
Author(s):  
Qing Bo Tian ◽  
Li Na Xu ◽  
Li Yang ◽  
Yan Sheng Yin
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Elevated Temperatures ◽  
Glass Ceramics ◽  
X Ray Diffraction ◽  
Crystallization Peak ◽  
X Ray ◽  
Microstructural Morphology ◽  
Microscopy Techniques ◽  
Scanning Electron

The influences of Fe2O3 doping on crystallization characteristics and microstructural morphology in the SiO2-Al2O3-MgO-K2O-ZrO2-F glass were investigated by using differential scanning calorimeter, X-ray diffraction and scanning electron microscopy techniques. The results indicate that the addtions of Fe2O3 shift the crystallization peaks to higher temperatures and the crystallization peaks increases in magnitude and the gap values between two crystallization peak temperatures boarden with the increment of Fe2O3 contents.The star-shaped crystals of cordietite by dendritic-manner growths are homogeneously precipitated in the rusidual glass. The mica phases, which are precipitated at interdendritic cordietite phases and formed the plate shapes at the elevated temperatures. The mica crystals grow at the expense of cordietite phases and finally form the composites of mica/cordietite uniformly distributed.

Effect of the Dwell Temperature on Spark Plasma Sintered CaCu3Ti4O12

2012 ◽  
Vol 727-728 ◽  
pp. 982-987
Author(s):  
E. de Carvalho ◽  
Marcelo Bertolete ◽  
Izabel Fernanda Machado ◽  
E.N.S. Muccillo
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Lattice Parameter ◽  
Solid State Reactions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Plasma Sintering ◽  
Spark Plasma ◽  
Diffraction Patterns ◽  
Scanning Electron

Polycrystalline CaCu3Ti4O12 ceramics were prepared by solid state reactions by spark plasma sintering (SPS) technique. In this study, the effects of the dwell temperature on structural, microstructural and dielectric properties of CaCu3Ti4O12 ceramics have been investigated. Powder mixtures were calcined at 900°C for 18 h before SPS consolidation. The dwell temperatures were 850, 900, 915 and 930°C. Sintered pellets were characterized by X-ray diffraction, scanning electron microscopy and impedance spectroscopy. X-ray diffraction patterns show evidences of a single-phase perovskite-type structure. The calculated lattice parameter is 7.40 Å. The hydrostatic density increases slightly with increasing dwell temperature. Scanning electron microscopy observations revealed a heterogeneous microstructure for all samples. The dielectric loss remains constant over a wide temperature range. The obtained permittivity is approximately 103 at 1 kHz. The increase of the dwell temperature is found to produce a brittle ceramic.

Halloysite in some soils from north-east Scotland

Clay Minerals ◽  
1977 ◽  
Vol 12 (1) ◽  
pp. 59-66 ◽  
Author(s):  
M. J. Wilson ◽  
J. M. Tait
Keyword(s):  
Electron Microscopy ◽  
Electron Diffraction ◽  
Soil Samples ◽  
X Ray Diffraction ◽  
X Ray ◽  
Drainage Class ◽  
North East ◽  
Parent Rocks ◽  
Diffraction Patterns

AbstractX-ray diffraction and electron microscopy show that halloysite occurs widely in soils derived from a variety of parent rocks (granite, gabbro, schist and slate) in north-east Scotland. Both tubular and non-tubular forms are observed, the latter being characterized by electron diffraction patterns with 001 reflection either absent or very weak and diffuse. Clay fractions from a poorly drained profile separated without prior drying of the soil samples contain essentially dehydrated halloysite at the surface, this becoming progressively more hydrated with depth. Since halloysite occurs extensively in soils of widely varying drainage class the mineral is probably not the result of recent soilforming processes but may have originated during Tertiary or interglacial weathering.

Ethylenediamine Processed Cu2SnS3 Nano Particles via Mild Solution Route

2016 ◽  
Vol 19 (1) ◽  
pp. 001-005 ◽  
Author(s):  
Paul Nesamony Prathiba Jeya Helan ◽  
Kannusamy Mohanraj ◽  
Sethuramachandran Thanikaikarasan ◽  
Thaiyan Mahalingam ◽  
Ganesan Sivakumar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Fourier Transform Infrared ◽  
Nano Particles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Electron Microscopy Analysis ◽  
Microscopy Techniques ◽  
Scanning Electron

Copper tin sulphide nanoparticles have been prepared by solution growth technique at various ethylenediamine concentrations. Prepared samples have been characterized using x-ray diffraction, fourier transform infrared, Raman and scanning electron microscopy techniques. x-ray diffraction results revealed that the prepared samples are nanocrystalline in nature with tetragonal structure. Fourier transform infrared spectroscopy analysis results showed the presence of Cu-O, Sn-O and Sn-S vibrations in the wavenumber range between 450 and 620 cm-1. Vibrational symmetry of prepared samples have been analyzed using Raman spectroscopy. Scanning electron microscopy analysis indicated the formation of flower like nanocrystals for samples prepared at various Ethylenediamine concentrations.

Deposition of TiO2 Thin Films Using Magnetron Sputtering

2011 ◽  
Vol 217-218 ◽  
pp. 1743-1746
Author(s):  
Xing Long Guo
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Magnetron Sputtering ◽  
Profile Analysis ◽  
Line Profile Analysis ◽  
Analysis Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Average Grain Size ◽  
Diffraction Patterns

TiO2 with 20nm in diameter have been prepared by using magnetron sputtering technique. The structure of these powers was determined by X-ray diffraction experiments. The average grain size and particle size in these powers were measured by the line profile analysis method of X-ray diffraction patterns and by scan electron microscopy, respectively. The thin films were investigated by using XRD, SEM measurements.

scholarly journals An electron microscopic and optical diffraction analysis of the structure of Limulus telson muscle thick filaments.

1982 ◽  
Vol 92 (2) ◽  
pp. 443-451 ◽  
Author(s):  
R W Kensler ◽  
R J Levine
Keyword(s):  
Electron Microscopy ◽  
Diffraction Analysis ◽  
Electron Micrographs ◽  
Optical Diffraction ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
X Ray ◽  
Thick Filaments ◽  
Diffraction Patterns ◽  
Cross Bridges

Long, thick filaments (greater than 4.0 micrometer) rapidly and gently isolated from fresh, unstimulated Limulus muscle by an improved procedure have been examined by electron microscopy and optical diffraction. Images of negatively stained filaments appear highly periodic with a well-preserved myosin cross-bridge array. Optical diffraction patterns of the electron micrographs show a wealth of detail and are consistent with a myosin helical repeat of 43.8 nm, similar to that observed by x-ray diffraction. Analysis of the optical diffraction patterns, in conjunction with the appearance in electron micrographs of the filaments, supports a model for the filament in which the myosin cross-bridges are arranged on a four-stranded helix, with 12 cross-bridges per turn or each helix, thus giving an axial repeat every third level of cross-bridges (43.8 nm).

scholarly journals Structural and In Situ X-ray Diffraction Study of Hydrogenation of CaxMg1−xNi2 (0 ≤ x ≤ 1)

Crystals ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 47
Author(s):  
Zia Ur Rehman ◽  
Mohsan Nawaz ◽  
Hameed Ullah ◽  
Pervaiz Ahmad ◽  
Mayeen Uddin Khandaker ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Powder Diffraction ◽  
Gas Flow ◽  
Hydrogen Gas ◽  
Laves Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Phase Type ◽  
Diffraction Patterns

In the quasi-binary system CaNi2-MgNi2 solid-solutions CaxMg1−xNi2 (0 ≤ x ≤ 1) were prepared from the elements. They crystallize in the hexagonal Laves phase type (MgNi2, C36) for x ≤ 0.33 (P63/mmc, a = 482.51(7) pm, c = 1582.1(3) pm for x = 0, a = 482.59 (3), c = 1583.1(1) for x = 0.33) and in the cubic Laves phase type (MgCu2, C15) for 0.33 < x (Fd−3m, a = 697.12(3) pm for x = 0.5, a = 705.11(2) pm for x = 0.67, a = 724.80(2) pm for x = 1). After hydrogenation in an autoclave the X-ray diffraction patterns changed completely. Reflections assigned to CaNiH3, and Ni and Rietveld refinement confirmed this. The hydrogenation properties of CaxMg1−xNi2 (0 ≤ x ≤ 1) compounds were also studied in situ by X-ray powder diffraction. In situ X-ray powder diffraction of CaxMg1−xNi2 (0 ≤ x ≤ 1) compounds under 0.3 MPa hydrogen gas flow (15 sccm), data collected on a Rigaku SmartLab diffractometer in an Anton Paar XRK 900 Reactor Chamber using Cu-Kα1 radiation. Scanning electron microscopy and EDX spectroscopy confirmed the entitled materials and elemental composition, respectively. From the Transmission electron microscopy and Selected area electron diffraction concluded that the CaxMg1−xNi2 (0 ≤ x ≤ 1) compounds were crystalline.

scholarly journals Crystal Chemistry of Carnotite in Abandoned Mine Wastes

Minerals ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 883 ◽  
Author(s):  
Sumant Avasarala ◽  
Adrian J. Brearley ◽  
Michael Spilde ◽  
Eric Peterson ◽  
Ying-Bing Jiang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Crystal Chemistry ◽  
Mine Waste ◽  
Atomic Ratio ◽  
Synthetic Analog ◽  
Mine Wastes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Degree Of Hydration ◽  
Diffraction Patterns

The crystal chemistry of carnotite (prototype formula: K2(UO2)2(VO4)2·3H2O) occurring in mine wastes collected from Northeastern Arizona was investigated by integrating spectroscopy, electron microscopy, and x-ray diffraction analyses. Raman spectroscopy confirms that the uranyl vanadate phase present in the mine waste is carnotite, rather than the rarer polymorph vandermeerscheite. X-ray diffraction patterns of the carnotite occurring in these mine wastes are in agreement with those reported in the literature for a synthetic analog. Carbon detected in this carnotite was identified as organic carbon inclusions using transmission electron microscopy (TEM) and electron energy loss spectroscopy (EELS) analyses. After excluding C and correcting for K-drift from the electron microprobe analyses, the composition of the carnotite was determined as 8.64% K2O, 0.26% CaO, 61.43% UO3, 20.26% V2O5, 0.38% Fe2O3, and 8.23% H2O. The empirical formula, (K1.66Ca0.043Al(OH)2+0.145 Fe(OH)2+0.044)((U0.97)O2)2((V1.005)O4)2·4H2O of the studied carnotite, with an atomic ratio 1.9:2:2 for K:U:V, is similar to the that of carnotite (K2(UO2)2(VO4)2·3H2O) reported in the literature. Lattice spacing data determined using selected area electron diffraction (SAED)-TEM suggests: (1) complete amorphization of the carnotite within 120 s of exposure to the electron beam and (2) good agreement of the measured d-spacings for carnotite in the literature. Small differences between the measured and literature d-spacing values are likely due to the varying degree of hydration between natural and synthetic materials. Such information about the crystal chemistry of carnotite in mine wastes is important for an improved understanding of the occurrence and reactivity of U, V, and other elements in the environment.

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