Characterization and Adsorption Efficiency of the Natural and the Modified Diatomite via the Low Temperature Hydrothermal Route

2012 ◽  
Vol 506 ◽  
pp. 425-428 ◽  
Author(s):  
Pusit Pookmanee ◽  
P. Thippraphan ◽  
P. Jansanthea ◽  
Sukon Phanichphant
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Low Temperature ◽  
Chemical Properties ◽  
Chemical Compositions ◽  
Adsorption Efficiency ◽  
Hydrothermal Route ◽  
X Ray ◽  
Modified Diatomite ◽  
Scanning Electron

Natural diatomite was modified by manganese chloride via the low temperature hydrothermal route. The chemical properties and adsorption efficiency of the natural and the modified diatomite were characterized. The chemical compositions of the natural and the modified diatomite were determined by X-ray fluorescence spectroscopy (XRF) and energy dispersive X-ray spectrometry (EDXS). Morphology of the natural and the modified diatomite was investigated by scanning electron microscopy (SEM). The adsorptions of Cd (II) and Pb (II) ions onto the natural and the modified diatomite were determined by atomic absorption spectroscopy (AAS).

Magnesium Nitrate as Additive for Synthesis of Mg(OH)2 Nanoparticles

2012 ◽  
Vol 198-199 ◽  
pp. 99-102
Author(s):  
Qing Gang Kong ◽  
Hai Yan Qian
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Low Temperature ◽  
Magnesium Nitrate ◽  
Crystal Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Size And Morphology ◽  
Scanning Electron

Magnesium nitrate was used as additive for synthesis of Mg(OH)2 (MH) nanoparticles at low temperature (70°C). Mg(OH)2 nanoparticles have platelet-like structure and approximately 40-60nm in thicknesses. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were applied to characterize the crystal phase. The supersaturation degree of solution effects the size and morphology of MH nanoparticles.

SiO2ZrO2 Thin Films as Low Temperature NO2 and O3 Sensors

2015 ◽  
Vol 1088 ◽  
pp. 81-85 ◽  
Author(s):  
T.N. Myasoedova ◽  
Victor V. Petrov ◽  
Nina K. Plugotarenko ◽  
Dmitriy V. Sergeenko ◽  
Galina Yalovega ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Scanning Electron Microscopy ◽  
Low Temperature ◽  
Annealing Temperature ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Operating Temperatures ◽  
Scanning Electron

Thin SiO2ZrO2films were prepared, up to 0.2 μm thick, by means of the sol–gel technology and characterized by a Scanning electron microscopy and X-ray diffraction. It is shown the presence of monoclinic, cubic and tetragonal phases of ZrO2in the SiO2matrix. The crystallites sizes depend on the annealing temperature of the film and amount to 35 and 56 nm for the films annealed at 773 and 973 K, respectively. The films resistance is rather sensitive to the presence of NO2and O3impurity in air at lower operating temperatures in the range of 30-60°C.

Effects of Mg2+ Doping on the Properties of LiFePO4 Synthesized via Hydrothermal Route

2009 ◽  
Vol 610-613 ◽  
pp. 498-501
Author(s):  
Guang Chuan Liang ◽  
Xiao Ke Zhi ◽  
Xiu Qin Ou ◽  
Li Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Cell Volume ◽  
X Ray Diffraction ◽  
Hydrothermal Route ◽  
X Ray ◽  
Charge Discharge ◽  
Scanning Electron ◽  
Discharge Test

Mg2+ doped LiFePO4 was synthesized from Li3PO4, FeSO4 and MgSO4 by a hydrothermal synthesis at 150 °C（Li1-xMgxPO4, x=0.00, 0.01,0.02,0.04,0.06）. The samples were characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM) and charge-discharge test. The results showed that Mg2+ dissolved in the LiFePO4 lattice. When the content is in the range of 0 to 6 mol%, Mg2+ caused the shrinkage of LiFePO4 cell volume. The capacity of doped and undoped samples at low discharging rate was similar, about 145mAhg-1 for 0.2C. But the sample doped with 2-4 mol% Mg2+ has higher capacity and longer cycle lifetime than the undoped one at 5C.

Nondestructive Characterization of Beryllium Effects on Ni-Cr Dental Alloy Elastic Properties and Microstructure: Ultrasonics, X-Ray Diffractometry, Scanning Electron Microscopy and Wavelength Dispersive Spectrometry

1988 ◽  
Vol 142 ◽  
Author(s):  
Surendra Singh ◽  
J. Lawrence Katz ◽  
B. S. Rosenblatt
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Elastic Properties ◽  
Ultrasonic Pulse ◽  
Chemical Compositions ◽  
Transmission Method ◽  
Buoyant Force ◽  
X Ray ◽  
Wavelength Dispersive Spectrometry ◽  
Scanning Electron

AbstractKnowledge of structure-properties relationship is a key factor in the development and improvement of new and existing metal alloys through manipulation in their chemical-compositions. In this study, the elastic properties and microstructure of cast Ni-Cr-Be and Ni-Cr dental alloys were studied. The elastic properties, i.e., Young's, shear and bulk moduli and Poisson's ratios, were determined using measurements on the ultrasonic velocities and densities. Both the shear and the longitudinal (dilatational) velocities were measured using an ultrasonic pulse-through-transmission method; density was measured using a buoyant force method. In microstructure, crystallinity, porosity, particle-size and quantitative elemental compositions were studied using x-ray diffractometry (XRD), scanning electron microscopy (SEM) and wavelength dispersive spectrometry (WDS) respectively. These results show that: (1) the addition of Be increased significantly the alloy's elastic moduli and Poisson's ratio; and (2) the presence of Be in Ni-Cr alloy also significantly modified its microstructure by producing a second binary phase, Ni-Be, in eutectic areas.

Intermetallic Alloys Ni3Si and Ni3(Si,Ti): Microstructures and Properties

2008 ◽  
Vol 368-372 ◽  
pp. 1143-1145 ◽  
Author(s):  
Ding Fan ◽  
Yao Ning Sun ◽  
Min Zheng ◽  
Jian Bin Zhang ◽  
Yu Feng Zheng
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Differential Scanning Calorimetry ◽  
Continuous Wave ◽  
Chemical Compositions ◽  
Intermetallic Alloys ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Scanning Electron

Laser cladding experiment was carried out with a 5 kW continuous wave CO2 laser by preplacing Ni75Si25 and Ni78Si13Ti9 powders onto Ni-based superalloy substrate. The microstructure of the specimens was monitored by using optical and scanning electron microscopy. The chemical compositions of the alloys and their phases were obtained using X-ray diffraction and energy dispersive x-ray spectroscopy. The phase transformation temperatures were determined by non-isothermal differential scanning calorimetry tests. The microhardness of the laser cladded sample was measured.

Synthesis and Characterization of NiO Doped SnO2 Nano-Flowers

2013 ◽  
Vol 575-576 ◽  
pp. 58-60
Author(s):  
Wei Ping Tang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectrum ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Hydrothermal Route ◽  
X Ray ◽  
Scanning Electron

In this present work, a new method for preparing NiO doped SnO2 nanoflowers by hydrothermal route is suggested. The composition and microstructure of samples were characterized by field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD) and Fourier transform infrared spectrum (FTIR). Moreover, a possible formation mechanism was discussed.

Characterization of Diatomite, Leonardite and Pumice

2016 ◽  
Vol 872 ◽  
pp. 211-215 ◽  
Author(s):  
Pusit Pookmanee ◽  
Atit Wannawek ◽  
Sakchai Satienperakul ◽  
Ratchadapon Putharod ◽  
Nattapol Laorodphan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Functional Group ◽  
Chemical Compositions ◽  
Carbonyl Groups ◽  
X Ray Diffraction ◽  
X Ray ◽  
Properties Of Materials ◽  
Scanning Electron

This research studies compositions of diatomite, leonardite and pumice for utilization appropriate to the properties of materials. Chemical compositions of these materials were characterized by X–ray fluorescence spectrometry (XRF) and energy dispersive X–ray spectrometry (EDXS). The silica was major component of these materials. The morphology was investigated by scanning electron microscopy (SEM). Diatomite was cylindrical in shape, leonardite was sheet or flake in shape and pumicewas prismatic in shape. The structure was studied by X–ray diffraction (XRD). It was found that the mineral composition of diatomite, leonardite and pumice showed cristobalite low, quartz and anorthite, respectively. The functional groups were identified by Fourier transform infraredspectrometry (FTIR). The functional group of siloxane was obtained and dominated vibration in these materials. And the vibration of carboxylic, alcoholic and carbonyl groups were obtained in leonardite.

Characterization of Superconducting Tunnel Junction X-ray Detectors by Low Temperature Scanning Electron Microscopy

1998 ◽  
Vol 37 (S2) ◽  
pp. 36 ◽  
Author(s):  
Masataka Ohkubo ◽  
Isao Sakamoto ◽  
Nobuyuki Hayashi ◽  
Jens Martin ◽  
Friedhelm Panteleit ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Low Temperature ◽  
Tunnel Junction ◽  
Superconducting Tunnel Junction ◽  
X Ray ◽  
Temperature Scanning ◽  
Scanning Electron

Synthesis of Na0.5Bi0.5TiO3 Microcubes via a Cr3+-Assisted Hydrothermal Route

2012 ◽  
Vol 463-464 ◽  
pp. 1497-1500
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Physical Properties ◽  
Hydrothermal Method ◽  
Significant Role ◽  
X Ray Diffraction ◽  
Hydrothermal Route ◽  
X Ray ◽  
Scanning Electron

Na0.5Bi0.5TiO3 microcubes with the side size ca. 20-30um were successfully fabricated by a Cr3+-assisted hydrothermal method. The obtained samples were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results show that Cr3+ played a significant role in the formation of Na0.5Bi0.5TiO3 microcubes. Possible mechanisms for the growth of Na0.5Bi0.5TiO3 microcubes are discussed. The results presented in this study would be important in investigating the correlation between morphology and basic physical properties, and may offer a route to control the morphology and size of crystals.

Study on the Properties of Poplar Micro/Nanofibril and its Composites

2012 ◽  
Vol 621 ◽  
pp. 48-53
Author(s):  
Yan Ping Liu ◽  
Jiang Tao Zhang ◽  
Xiao Ya Luo ◽  
Ying Ying Yao
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Wheat Straw ◽  
Internal Bond ◽  
Urea Formaldehyde ◽  
Formaldehyde Resin ◽  
Chemical Compositions ◽  
X Ray ◽  
Scanning Electron

The micro/nanofibrils of poplar could be prepared by treatment of ultrasonic. The properties of micro/nanofibrils were characterized by using scanning electron microscopy (SEM) and X-ray diffractometer (XRD). The results indicated that poplar micro/nanofibril was the same as raw fiber in chemical compositions and crystal structure. The crystallinity of micro/nanofibrils was 84.99 percent, increased by 20 percent compared to original fiber after ultrasonic crushing. The micro/nanofibril diameter was from 50 nm to 1 μm.The internal bond strength (IB) of wheat-straw fiberboard could be significantly improved by adding poplar micro/nanofibril suspension to the urea formaldehyde resin adhesive(UF),when the adding amount of poplar micro/nanofibril suspension was 15wt percent, the IB of wheat-straw fiberboard was up to 0.86 MPa.

Sign in / Sign up

Export Citation Format

Share Document