ChemInform Abstract: Multianvil Synthesis, X-Ray Powder Diffraction Analysis, 31P-MAS-NMR, and FTIR Spectroscopy as well as Material Properties of γ-P3N5, a High-Pressure Polymorph of Binary Phosphorus(V) Nitride, Built-Up from Distorted PN5 Square Pyrami

ChemInform ◽  
2010 ◽  
Vol 33 (41) ◽  
pp. no-no
Author(s):  
Kai Landskron ◽  
Hubert Huppertz ◽  
Juergen Senker ◽  
Wolfgang Schnick
1993 ◽  
Vol 49 (2) ◽  
pp. 169-171 ◽  
Author(s):  
Yu. A. Barabanenkov ◽  
N. D. Zakharov ◽  
I. P. Zibrov ◽  
V. P. Filonenko ◽  
P. Werner ◽  
...  

2017 ◽  
Vol 43 (5) ◽  
pp. 2752 ◽  
Author(s):  
E. Theodosoglou ◽  
A. Koroneos ◽  
T. Soldatos ◽  
T. Zorba ◽  
K. M. Paraskevopoulos

Natural K-feldspars from igneous rocks have been examined by means of X-ray powder diffraction(XRPD) and Fourier transform infrared (FTIR) spectroscopy in the spectral range 400-1400 cm-1,where the Si-Al-O bonds exhibit the dominant vibrations. From the XRPD analysis three specieshave been distinguished, i.e. microclines (3 samples), orthoclases (4 samples) and sanidines (3 samples);their unit cell parameters were calculated. The FTIR transmittance spectra of all sampleshave common bands at 426, 463, 584, 604, 726 and 772 cm-1 and some additional features. The spectraof sanidine and orthoclase exhibit fewer and broader bands than the microclines’, especially inthe area 1000-1200 cm-1. The differences in their spectra are located in four bands. The bands ataround 536-538 and 646-648 cm-1 in the spectrum of microcline, are shifted at around 542-544 and640-642 cm-1 in the spectrum of orthoclase and at around 546 and 636 cm-1 in the spectrum of sanidine.Four bands at 1010, 1050, 1090 and 1136 cm-1 in the spectra of microcline are substitutedwith two quite broad bands at about 1030 and 1125 cm-1 in the spectra of orthoclase and sanidine.These differences are attributed to different degree of Al-Si ordering in the structure of K-feldspars.


2008 ◽  
Vol 591-593 ◽  
pp. 392-396 ◽  
Author(s):  
Luís Gallego Martinez ◽  
J.L. Rossi ◽  
M.T.D. Orlando ◽  
C.A.C. Passos ◽  
Francisco Cristóvão Lourenço de Melo ◽  
...  

Samples of the superconducting ceramics Hg0.82Re0.18Ba2Ca2Cu3O8+ were prepared by solid-vapor reaction technique. The preparation of the ceramic precursor started with a mixture of Ba2Ca2Cu3Ox and ReO2 powders with molar ratio 1:0.18. The precursor material was submitted to annealing under three different partial pressures of oxygen using a mixture of oxygen/argon at ratios: 5/95 (sample A), 10/90 (sample B) and 15/85 (sample C). X-ray powder diffraction analysis of the precursors identified the phases BaCuO2+x, Ba2Cu3O5+x, Ba4CaCu3O8+x, Ca2CuO3 and Ca5Re2O12 at different ratios in the samples, indicating an increment in the oxygen content from sample A to sample C. Finally, the precursors with different oxygen contents were blended with HgO at molar ratio 1:0.82 and treated in a sealed high pressure furnace to produce the high Tc superconducting ceramics. Rietveld refinement of XRD data showed differences in the crystal structures of the samples. The measurement of thermopower at room temperature resulted in distinct values, confirming the different oxygen sample doping.


2020 ◽  
Author(s):  
Miranda Maliszka ◽  
◽  
Sabrina Sobel ◽  
Anthony Johnson ◽  
Dennis Radcliffe

1993 ◽  
Vol 6 (11) ◽  
pp. 803-806 ◽  
Author(s):  
A A Qidwai ◽  
M Humayun ◽  
M W Akhtar ◽  
D Ahmad ◽  
A Saghir

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