Structure Characteristics Analysis of Long Flame Coal

2013 ◽  
Vol 724-725 ◽  
pp. 1046-1049
Author(s):  
Yang Bo Deng ◽  
Zhen Xu ◽  
Jing Ming Dong
Keyword(s):  
Diffraction Peak ◽  
X Ray Diffraction ◽  
Aromatic Rings ◽  
X Ray ◽  
Structure Characteristics ◽  
Characteristics Analysis ◽  
Crystallite Structure

Applying X-ray diffraction, an analysis of crystallite structure on the coal samples from Hami, including raw coal and coals heated respectively at 200°C, 250°C and 300°C, was carried out. The results show: The intensity of the 002 diffraction peak increases, the γ diffraction peak of the coals decreases, the 100 diffraction peak appears and its intensity increases, the size of the crystallite, the stacking height of the aromatic layer and the condensation degree of the aromatic rings increase, and the proportion of the non-crystallite decreases in coal samples, with the temperature increasing at below 300°C.

Low Molecular Weight Microfibers with Light Sensing Properties

2017 ◽  
Vol 54 (4) ◽  
pp. 655-658
Author(s):  
Andrei Bejan ◽  
Dragos Peptanariu ◽  
Bogdan Chiricuta ◽  
Elena Bicu ◽  
Dalila Belei
Keyword(s):  
Molecular Weight ◽  
Low Molecular Weight ◽  
X Ray Diffraction ◽  
Aromatic Rings ◽  
X Ray ◽  
Force Microscopy ◽  
Light Sensing ◽  
Sensing Applications ◽  
Atomic Force ◽  
Low Molecular Weight Compounds

Microfibers were obtained from organic low molecular weight compounds based on heteroaromatic and aromatic rings connected by aliphatic spacers. The obtaining of microfibers was proved by scanning electron microscopy. The deciphering of the mechanism of microfiber formation has been elucidated by X-ray diffraction, infrared spectroscopy, and atomic force microscopy measurements. By exciting with light of different wavelength, florescence microscopy revealed a specific optical response, recommending these materials for light sensing applications.

Problems Associated with Kα Doublet in Residual Stress Measurements

1979 ◽  
Vol 23 ◽  
pp. 333-339
Author(s):  
S. K. Gupta ◽  
B. D. Cullity
Keyword(s):  
Residual Stress ◽  
Silicon Powder ◽  
Lattice Parameter ◽  
Diffraction Peak ◽  
Parameter Determination ◽  
X Ray Diffraction ◽  
X Ray ◽  
Analysis Techniques ◽  
The Difference ◽  
Similar Accuracy

Since the measurement of residual stress by X-ray diffraction techniques is dependent on the difference in angle of a diffraction peak maximum when the sample is examined consecutively with its surface at two different angles to the diffracting planes, it is important that these diffraction angles be obtained precisely, preferably with an accuracy of ± 0.01 deg. 2θ. Similar accuracy is desired in precise lattice parameter determination. In such measurements, it is imperative that the diffractometer be well-aligned. It is in the context of diffractometer alignment with the aid of a silicon powder standard free of residual stress that the diffraction peak analysis techniques described here have been developed, preparatory to residual stress determinations.

W-Doped TiO2 Preparation and Photocatalytic Degradation of Guaiacol

2014 ◽  
Vol 513-517 ◽  
pp. 33-36 ◽  
Author(s):  
Zi Chang Xie ◽  
Ying Wang ◽  
Peng Wang ◽  
Lei Zhang
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Degradation Rate ◽  
Amorphous State ◽  
X Ray Diffraction ◽  
Model Compounds ◽  
Plant Fibers ◽  
X Ray ◽  
Crystallite Structure

In this paper, W-doped TiO2 (W-TiO2) powder was prepared in hydrothermal method by mixing TiO2 and ammonium metatungstate. The catalysts were characterized by X-ray diffraction and ultraviolet spectrophotometer. The results displayed that W-TiO2 showed an anatase crystallite structure with 2 % W content. W-element in W-TiO2 was amorphous state. The guaiacol was degraded with the W-TiO2 in the visible light. It was a model compounds of lignin existed in the plant fibers. The degradation rate of guaiacol was increased with the photocatalytic time, as high as 88.21 % after 360 min irradiation. It was concluded that the W-TiO2 had an obvious photocatalytic activity under visible light. It can be used in the photocatalytic degradation of lignin.

Transparent Conductive Cu-In-O Thin Films Deposited by Reactive DC Magnetron Sputtering with Different Targets

2011 ◽  
Vol 239-242 ◽  
pp. 2752-2755
Author(s):  
Fan Ye ◽  
Xing Min Cai ◽  
Fu Ping Dai ◽  
Dong Ping Zhang ◽  
Ping Fan ◽  
...  
Keyword(s):  
Thin Films ◽  
Magnetron Sputtering ◽  
Optical Band Gap ◽  
Diffraction Peak ◽  
X Ray Diffraction ◽  
Dc Magnetron Sputtering ◽  
Flow Rates ◽  
X Ray ◽  
Equal Distance ◽  
Transmittance Curve

Transparent conductive Cu-In-O thin films were deposited by reactive DC magnetron sputtering. Two types of targets were used. The first was In target covered with a fan-shaped Cu plate of the same radius and the second was Cu target on which six In grains of 1.5mm was placed with equal distance between each other. The samples were characterized with scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), UV/VIS spectrophotometer, four-probe measurement etc. SEM shows that the surfaces of all the samples are very smooth. EDX shows that the samples contain Cu, In as well as O, and different targets result in different atomic ratios of Cu to In. A diffraction peak related to rhombohedra-centered In2O3(012) is observed in the XRD spectra of all the samples. For both the two targets, the transmittance decreases with the increase of O2flow rates. The direct optical band gap of all the samples is also estimated according to the transmittance curve. For both the two targets, different O2flow rates result in different sheet resistances and conductivities. The target of Cu on In shows more controllability in the composition and properties of Cu-In-O films.

Microwave-assisted solvent-free synthesis and spectral and structural characterization of cyclotriphosphazene hexakis(o-tolylamide)

2018 ◽  
Vol 73 (12) ◽  
pp. 999-1003 ◽  
Author(s):  
Mohammad Hakimi ◽  
Homeyra Rezaei ◽  
Keyvan Moeini ◽  
Heidar Raissi ◽  
Vaclav Eigner ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Microwave Irradiation ◽  
Stacking Interactions ◽  
X Ray Diffraction ◽  
Aromatic Rings ◽  
X Ray ◽  
Microwave Assisted ◽  
Ft Ir ◽  
Solvent Free Synthesis

AbstractA new cyclotriphosphazene, 2,2,4,4,6,6-hexakis (o-tolylamono)-1,3,5,2λ5,4λ5,6λ5-triazatriphosphinine (MPAP), was prepared using microwave irradiation and identified by elemental analysis, FT-IR, Raman, 31P NMR spectroscopy, and single-crystal X-ray diffraction. In the crystal, in addition to hydrogen bonds, the network is further stabilized by inter- and intramolecular π–π stacking interactions between aromatic rings.

Relationships between molecular structure and physical properties in bent-core mesogens

2006 ◽  
Vol 364 (1847) ◽  
pp. 2657-2679 ◽  
Author(s):  
Wolfgang Weissflog ◽  
H.N Shreenivasa Murthy ◽  
Siegmar Diele ◽  
Gerhard Pelzl
Keyword(s):  
Optical Measurements ◽  
Polar Phase ◽  
X Ray Diffraction ◽  
Aromatic Rings ◽  
Scanning Calorimetry ◽  
Polarizing Microscopy ◽  
X Ray ◽  
Smectic Phases ◽  
Collective Rotation ◽  
Clear Change

New five-ring bent-core mesogens that possess only ester connecting groups between the aromatic rings and different lateral substituents at the central phenyl ring are presented. The mesophases have been assigned by polarizing microscopy, differential scanning calorimetry, X-ray diffraction and electro-optical measurements. It is shown that the mesophase behaviour depends strongly on the position of the lateral substituents. Compounds, which are derived from 4-cyano-, 4-chloro- and 4,6-dichloro-resorcinol, show polymorphism variants where polar phases (SmAP, SmCP) occur together with nematic and conventional smectic phases, e.g. SmA–SmAP, SmA–SmC S P A –Col ob –SmC S P A , N–SmA–SmCP A , SmA–SmC–SmCP A and SmC–SmCP A . On the basis of the behaviour of two series of materials, the occurrence of different polar-switching mechanisms could be demonstrated. Apart from the usual mechanism by director rotation around the tilt cone, the polar switching can also take place through collective rotation of the molecules around their long axes, which corresponds to a field-induced switching of the layer chirality. A remarkable finding is the polar switching in the crystalline modification of long-chain, bent-core compounds with a methyl group in 2-position, which is accompanied by a clear change of the optical texture and by a relatively high switching polarization (approx. 600 nC cm −2 ). It was found for selected bent-core compounds that, above the transition temperature of a polar to a non-polar phase, the non-polar phase can be transformed to the polar phase by application of an electric field, which was proved for the transitions isotropic–SmCP F , SmA–SmCP F and isotropic–CrII polar.

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