scholarly journals Copper-Containing Agates of the Avacha Bay (Eastern Kamchatka, Russia)

Minerals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1124
Author(s):  
Galina Palyanova ◽  
Evgeny Sidorov ◽  
Andrey Borovikov ◽  
Yurii Seryotkin

The copper-containing agates of the Avacha Bay (Eastern Kamchatka, Russia) have been investigated in this study. Optical microscopy, scanning electron microscopy, electron microprobe analysis, X-ray powder diffraction, Raman spectroscopy, and fluid inclusions were used to investigate the samples. It was found that copper mineralization in agates is represented by native copper, copper sulphides (chalcocite, djurleite, digenite, anilite, yarrowite, rarely chalcopyrite) and cuprite. In addition to copper minerals, sphalerite and native silver were also found in the agates. Native copper is localized in a siliceous matrix in the form of inclusions usually less than 100 microns in size—rarely up to 1 mm—forming dendrites and crystals of a cubic system. Copper sulphides are found in the interstices of chalcedony often cementing the marginal parts of spherule aggregates of silica. In addition, they fill the micro veins, which occupy a cross-cutting position with respect to the concentric bands of chalcedony. The idiomorphic appearance of native copper crystals and clear boundaries with the silica matrix suggest their simultaneous crystallization. Copper sulphides, cuprite, and barite micro veins indicate a later deposition. Raman spectroscopy and X-ray powder diffraction results demonstrated that the Avacha Bay agates contained cristobalite in addition to quartz and moganite. The fluid inclusions study shows that the crystalline quartz in the center of the nodule in agates was formed with the participation of solutions containing a very low salt concentration (<0.3 wt.% NaCl equivalent) at the temperature range 110–50 °C and below. The main salt components were CaCl2 and NaCl, with a probable admixture of MgCl2. The copper mineralization in the agates of the Avacha Bay established in the volcanic strata can serve as a direct sign of their metallogenic specialization.

2006 ◽  
Vol 988 ◽  
Author(s):  
Joshu A. Kurzman ◽  
Margret J. Geselbracht

AbstractTwo new Dion-Jacobson type layered perovskite solid solutions, RbCa2-xSrxM3O10 (M = Nb, Ta; 0 ≤ x ≤ 2), were prepared and studied by X-ray powder diffraction, neutron powder diffraction, and Raman spectroscopy. X-ray powder diffraction confirmed single-phase solid solution formation with continuous expansion of the idealized primitive tetragonal unit cell with increasing strontium content. Neutron powder diffraction studies of selected samples revealed lower symmetries and larger unit cells, as necessitated by octahedral tilting within the perovskite slabs, compared to the idealized primitive cell. As the average size of the A-cation in the perovskite slab is varied from Sr2+ to Ca2+, more extensive octahedral tilting is introduced. Vibrational modes of the perovskite slab observed using Raman spectroscopy show subtle changes as a function of calcium/strontium content and more intriguing differences between the isostructural niobates and tantalates.


2018 ◽  
Vol 20 (5) ◽  
pp. 3630-3636 ◽  
Author(s):  
C. Cappuccino ◽  
P. P. Mazzeo ◽  
T. Salzillo ◽  
E. Venuti ◽  
A. Giunchi ◽  
...  

This work presents a Raman based approach for the rapid identification of the molecular conformation in a series of new 2,3-thienoimide capped quaterthiophenes.


1998 ◽  
Vol 108 (9) ◽  
pp. 655-660 ◽  
Author(s):  
G.A. Tompsett ◽  
R.J. Phillips ◽  
N.M. Sammes ◽  
A.M. Cartner

2021 ◽  
Vol 29 (2) ◽  
pp. 241-248
Author(s):  
Jiří Sejkora ◽  
Roman Gramblička

The zýkaite samples were found at abandoned Lehnschafter mine near Mikulov in the Krušné hory Mts. (Czech Republic). It occurs as irregular white to light greenish rounded to spherical aggregates up to 1.5 cm in size composed of tiny acicular crystals up to 5 - 10 μm in length. Its empirical formula can be expressed as (Fe3.79Al0.02)Σ3.81[(AsO4)2.66(PO4)0.20(SiO4)0.07]Σ2.93 (SO4)1.07(OH)0.44·15H2O (mean of 3 spot analyzes; on the basis of As+P+S+Si = 4 apfu).Zýkaite is probably monoclinic, with the unit-cell parameters refined from X-ray powder diffraction data: a 21.195(8), b 7.052(2), c 36.518(17) Å, β 91.07(2)° and V 5458(2) Å3. Raman spectroscopy documented the presence of both (AsO4)3- and (SO4)2- units in the crystal structure of zýkaite. Multiple Raman bands connected with vibrations of water molecules and (AsO4)3- groups indicate the presence of more structurally non-equivalent these groups in the crystal stucture of zýkaite.


The Analyst ◽  
1997 ◽  
Vol 122 (1) ◽  
pp. 33-38 ◽  
Author(s):  
Christos G. Kontoyannis ◽  
Malvina G. Orkoula ◽  
Petros G. Koutsoukos

2012 ◽  
Vol 1372 ◽  
Author(s):  
David A. Miranda ◽  
S. A. López-Rivera ◽  
Ch. Power ◽  
J. A. Henao ◽  
M. A. Macías

ABSTRACTPhonons and crystalline structures of Hg1−xCdxSe alloys (0 ≤ x ≤ 0.5) were studied by Raman spectroscopy and X-ray powder diffraction patterns at 298K. The crystalline alloys were prepared by a special combination of synthesis and the Bridgman method. Experimental data showed a face-centered cubic structure, $F\overline 4 \,3\,m$ (No. 216), for all samples, exhibiting a linear dependence for Cd molar fraction, x, for cell parameters, a, and the mass densities, ρ. Phonon frequencies were analyzed using the Romevi-Romevi model for phonons in multicomponent alloys, obtaining a fair agreement with experimental data. Furthermore, an algorithm to implement the Romevi-Romevi model is proposed.


2008 ◽  
Vol 47-50 ◽  
pp. 1193-1196
Author(s):  
De Hui Sun ◽  
Hong Jie Zhang ◽  
Ji Lin Zhang ◽  
Jiang Bo Yu

The ethylenediamine trimolybdate (ENTMo) can show unusually photochromic and thermochromic properties and there exists in the difference of chromic mechanisms, which has been proved in our previous work [1]. In this paper, X-ray powder diffraction (XRD), Fourier transform infrared (FTIR) and laser Raman spectroscopy (LRS) of the colored samples are characterized and analyzed in detail. The crystal structure, the inorganic skeleton and the microenvironment of center ions of the colored samples do not substantively change except distortion. The color difference of the photochromic and the thermochromic samples is discussed and that the difference of reduction sites result in their different chromic mechanisms is suggested.


1990 ◽  
Vol 25 (11) ◽  
pp. 1311-1320 ◽  
Author(s):  
B. Borzęcka-Prokop ◽  
E. Kapturkiewicz ◽  
A. Weselucha-Birczynska ◽  
S. A. Hodorowicz

1999 ◽  
Vol 145 (2) ◽  
pp. 394-400 ◽  
Author(s):  
Frank J. Berry ◽  
Stephen J. Skinner ◽  
Ian M. Bell ◽  
Robin J.H. Clark ◽  
Clive B. Ponton

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