scholarly journals La2Ga3O7.5: A Metastable Ternary Melilite with a Super-Excess of Interstitial Oxide Ions Synthesized by Direct Crystallization of the Melt

2020 ◽  
Vol 32 (20) ◽  
pp. 9016-9025
Author(s):  
Jintai Fan ◽  
Vincent Sarou-Kanian ◽  
Xiaoyan Yang ◽  
Maria Diaz-Lopez ◽  
Franck Fayon ◽  
...  
1992 ◽  
Vol 96 (1) ◽  
pp. 691-699 ◽  
Author(s):  
Carolyn J. Cassady ◽  
David A. Weil ◽  
Stephen W. McElvany
Keyword(s):  

2018 ◽  
Vol 20 (12) ◽  
pp. 8008-8015 ◽  
Author(s):  
J. P. Parras ◽  
A. R. Genreith-Schriever ◽  
H. Zhang ◽  
M. T. Elm ◽  
T. Norby ◽  
...  

Unexpected behaviour of the migration energetics of oxide ions, hydronium ions and lithium ions in perovskite-structured ReO3.


1986 ◽  
Vol 40 (4) ◽  
pp. 434-445 ◽  
Author(s):  
M. A. Vaughan ◽  
G. Horlick

In inductively coupled plasma/mass spectrometry analyte, M may be distributed among several species forms including doubly charged ions (M2+), singly charged ions (M+), mono-oxide ions (MO+), and hydroxide ions (MOH+). Detailed data are presented for Ba to illustrate the dependence of the ion count of these species and their ratios (M2+/M+, MO+/M+, and MOH+/M+) on nebulizer flow rate, plasma power, and sampling depth. Although these data are representative of most elements, many form oxides to a much greater degree than Ba; data are presented for Ti, W, and Ce to illustrate this fact. These various analyte species are important in that serious interelement interferences can occur because of spectral overlap. An extensive pair of tables indicating potential spectral interferences caused by element oxide, hydroxide, and doubly charged ions is presented.


2016 ◽  
Vol 2016 ◽  
pp. 1-13 ◽  
Author(s):  
Manuel Sánchez-Cantú ◽  
Clara Barcelos-Santiago ◽  
Claudia M. Gomez ◽  
Esthela Ramos-Ramírez ◽  
Ma. de Lourdes Ruiz Peralta ◽  
...  

Three hydrocalumite-like compounds in a Ca/Al ratio of 2 containing nitrate and acetate anions in the interlaminar region were prepared by a simple, economic, and environmentally friendly method. The solids were characterized by X-ray powder diffraction (XRD), thermogravimetric (TG) analysis, nitrogen adsorption-desorption at −196°C, scanning electron microscopy (SEM), infrared spectroscopy (FTIR), and UV-Vis Diffuse Reflectance Spectroscopy (DRS). The catalytic activity of the calcined solids at 700°C was tested in the photodegradation of 2,4-dichlorophenoxyacetic acid (2,4-D) where 57% degradation of 2,4-D (40 ppm) and a mineralization percentage of 60% were accomplished within 150 minutes. The photocatalytic properties were attributed to mayenite hydration, since the oxide ions in the cages are capable of reacting with water to form hydroxide anions capable of breaking down the 2,4-D molecules.


2013 ◽  
Vol 160 (9) ◽  
pp. E90-E93 ◽  
Author(s):  
Yuya Kado ◽  
Takuya Goto ◽  
Rika Hagiwara

2000 ◽  
Vol 658 ◽  
Author(s):  
A. Manthiram ◽  
R. V. Chebiam ◽  
F. Prado

ABSTRACTLayered Co1-yNiyO2-δ oxides with 0≤y≤1 have been synthesized by chemically extracting lithium from LiNi1-yCoyO2 with NO2PF6 at ambient temperature. The samples have been characterized by X-ray diffraction, wet-chemical analyses, infrared spectroscopy, and magnetic susceptibility measurements. While NiO2-δ retains the initial O3 (CdCl2 structure) layer structure of LiNiO2, CoO2-δ consists of a mixture of P3 and O1 (CdI2 structure) phases that are formed by a sliding of the oxide ions in the initial O3 structure. CoO2-δ and NiO2-δ have oxygen contents of, respectively, 1.67 and 1.95 and the oxygen content increases with increasing Ni content, y, in Co1-yNiyO2-δ. While CoO2-δ exhibits metallic conductivity as revealed by theabsence of absorption bands in the infrared spectrum, NiO2-δ exhibits semiconducting behavior due to a completely filled t2g band. Magnetic data reveal a transition from antiferromagnetic to ferromagnetic correlations as the Ni content in Co1-yNiyO2-δ increases.


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