Neutron Diffraction Studies on the Structure and Conduction Mechanism in Al, Ga—DOPED Li4SiO4

1990 ◽  
Vol 210 ◽  
Author(s):  
R.I. Smith ◽  
A.R. West

AbstractCrystallographic results on the Li4-3x(Al,Ga)xSiO4 solid solutions are reviewed. The six sets of sites available for Li+ ions fall into two groups. The ‘framework’ sites, which also contain the substitutional Al,Ga ions, appear to have little effect on conductivity. The ‘channel’sites contain varying amounts of Li+ ions and are responsible for the dramatic variations in conductivity with x. There is evidence for the presence of one—dimensional defects, comprising columns of ordered Li+ ions, in both the framework and channel sites. The relative numbers of these linear defects has a large bearing on the solid solution mechanism in the framework sites and their occurrence in the channel sites may be responsible for the low conductivity in stoichiometric Li4SiO4.

Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 640
Author(s):  
Hideaki Sasaki ◽  
Keisuke Sakamoto ◽  
Masami Mori ◽  
Tatsuaki Sakamoto

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.


2020 ◽  
Vol 58 (1) ◽  
pp. 71-83
Author(s):  
Elahe Mansouri Gandomani ◽  
Nematollah Rashidnejad-Omran ◽  
Amir Emamjomeh ◽  
Pietro Vignola ◽  
Tahereh Hashemzadeh

ABSTRACT Turquoise, CuAl6(PO4)4(OH)8·4H2O, belongs to the turquoise group, which consists of turquoise, chalcosiderite, aheylite, faustite, planerite, and UM1981-32-PO:FeH. In order to study turquoise-group solid solutions in samples from the Neyshabour and Meydook mines, 17 samples were selected and investigated using electron probe microanalysis. In addition, their major elements were compared in order to evaluate the feasibility of distinguishing the provenance of Persian turquoises. The electron microprobe data show that the studied samples are not constituted of pure turquoise (or any other pure endmember) and belong, from the chemical point of view, to turquoise-group solid solutions. In a turquoise–planerite–chalcosiderite–unknown mineral quaternary solid solution diagram, the chemical compositions of the analyzed samples lie along the turquoise–planerite line with minor involvement of chalcosiderite and the unknown mineral. Among light blue samples with varying hues and saturations from both studied areas, planerite is more abundant among samples from Meydook compared with samples from Neyshabour. Nevertheless, not all the light blue samples are planerite. This study demonstrates that distinguishing the deposit of origin for isochromatic blue and green turquoises, based on electron probe microanalysis method and constitutive major elements, is not possible.


1994 ◽  
Vol 341 ◽  
Author(s):  
E. S. Hellman ◽  
E. H. Hartford

AbstractMetastable solid-solutions in the MgO-CaO system grow readily on MgO at 300°C by molecular beam epitaxy. We observe RHEED oscillations indicating a layer-by-layer growth mode; in-plane orientation can be described by the Matthews theory of island rotations. Although some films start to unmix at 500°C, others have been observed to be stable up to 900°C. The Mgl-xCaxO solid solutions grow despite a larger miscibility gap in this system than in any system for which epitaxial solid solutions have been grown. We describe attempts to use these materials as adjustable-lattice constant epitaxial building blocks


2004 ◽  
Vol 2004 (14) ◽  
pp. 2943-2949 ◽  
Author(s):  
Dejana Vujovic ◽  
Helgard G. Raubenheimer ◽  
Luigi R. Nassimbeni

Author(s):  
Christopher H. Ingles ◽  
John A. Mavrogenes

ABSTRACT Laser ablation-inductively coupled plasma-mass spectrometry was used to traverse hydrothermal vein sphalerite from different ore-forming stages of the Porgera Au-Ag mine, Papua New Guinea. Elements were measured in situ over the growth of crystals to investigate the greatly varying concentrations of cations in sphalerite and their positions in the lattice. Traverse profiles for 16 elements were obtained and aligned to transmitted light images where possible. Each sample contained an array of elements, with many displaying orders of magnitude concentration differences. Results show the simultaneous incorporation of Cu and Sn in sphalerite, as well as Cu and Ag, In and Sn, As and Sb, Fe and Mn, and Cu and Ga. The relation [4Zn2+ ↔ 2Cu+ + Sn2+ + Sn4+] is proposed to explain the 1:1 Cu–Sn correlation. Further relations can be seen, including a Ga “ceiling” or Cu “floor”, where Ga incorporation becomes dependent on Cu concentrations. Furthermore, silver was also observed to correlate with Au, Mn, Ni, Pb, and Bi. Meta-stable solid solutions between pairs such as Cu, Ag; Fe, Mn; As, Sb; and In, Sn are also suggested. Each of these pairs are neighbors on the periodic table of elements, which suggests that simple solid solution can occur, and positive correlations for all four solid solutions were found in one sample alone. While the concept of charge-specific solid solutions in sphalerite has been discussed in the literature with reference to monovalent cations, the results presented herein also indicate solid solutions of higher oxidation states, containing many cations. Furthermore, while cations in charge-specific solid solutions have been proposed to compete for lattice sites in sphalerite, simultaneous in situ coupled concentrations at Porgera suggest otherwise. Cationic substitution equations displaying decimal ratios of each element in solid solution can then provide a novel method to distinguish between solid solution concentrations in different samples. For example, displaying 1:1 ratios of Cu–Ag and Sb–As: [2Zn2+ ↔ (Cu+0.5, Ag+0.5) + (As3+0.5, Sb3+0.5)], or for a 100:1 Fe–Mn ratio: [Zn2+ ↔ (Fe2+0.99, Mn2+0.01)].


2008 ◽  
Vol 2008 ◽  
pp. 1-4 ◽  
Author(s):  
Yurong Wu ◽  
Wangyu Hu

Molecular dynamic simulations have been performed to study the solid solution mechanism of Mg100-xREx (RE=Gd,Dy,Y, x=0.5,1,2,3,4  at.%). The obtained results reveal that the additions of Gd, Dy and Y increase the lattice constants of Mg-RE alloys. Also the axis ratio c/a remains unchanged with increase in temperature, restraining the occurrence of nonbasal slip and twinning. Furthermore, it is confirmed that bulk modulus of Mg alloys can be increased remarkably by adding the Gd, Dy, Y, especially Gd, because the solid solubility of Gd in Mg decrease sharply with temperature in comparison with Dy and Y. Consequently, the addition of the RE can enhance the strength of Mg-based alloys, which is in agreement with the experimental results.


2001 ◽  
Vol 70 (5) ◽  
pp. 1222-1225 ◽  
Author(s):  
Seiji Niitaka ◽  
Hiroshi Kageyama ◽  
Kazuyoshi Yoshimura ◽  
Koji Kosuge ◽  
Shinji Kawano ◽  
...  

1998 ◽  
Vol 13 (4) ◽  
pp. 939-943 ◽  
Author(s):  
Junfeng Ma ◽  
Masahiro Yoshimura ◽  
Masato Kakihana ◽  
Masatomo Yashima

A series of solid solutions (1 − x) ZrO2 · xY0.857 W0.143 O1.714 (1/7Y6WO12) of metastable cubic phase were synthesized at 800 °C through a polymerized complex method. Lattice parameter a0 of solid solutions varies linearly with Y0.857 W0.143 O1.714 content (x). Crystallization began to occur above 400 °C from amorphous precursor to yield at 800 °C fine powders of 6–10 nm and 19–40 m2/g for crystallite size and surface area, respectively.


1975 ◽  
Vol 17 (1) ◽  
pp. 45-48 ◽  
Author(s):  
J.M. Williams ◽  
F.K. Ross ◽  
M. Iwata ◽  
J.L. Petersen ◽  
S.W. Peterson ◽  
...  

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