Results of study of crystallographic orientation of olivine and diamond from Udachnaya kimberlite pipe,Yakutia     

Yu. V. Seryotkin  V. L. Skvortsova  A. M. Logvinova  N. V. Sobolev 《Doklady Earth Sciences》2017,476(2):1155-1158

The crystallographic orientation of three diamonds and 19 olivine inclusions from Udachnaya kimberlite pipe was studied using monocrystal X-ray diffractometry. No epitaxial olivine inclusions were found.  相似文献   

IR spectroscopic characterization of NH4-analcime     

A. Yu. Likhacheva  E. A. Paukshtis  Yu. V. Seryotkin  S. G. Shulgenko 《Physics and Chemistry of Minerals》2002,29(9):617-623

 The IR spectrum of ammonium-exchanged natural analcime (basalt, Nidym River, Siberian platform) exhibits several features that suggest a lowered symmetry for the NH₄ ⁺ ion and that this is influenced by hydrogen bonding within the framework. These features are: the pronounced splitting into three components and high-frequency shift of the ν₄-bending mode; appearance of the ν₁-stretching mode which is predicted to become IR-active when the ideal T _d symmetry of NH₄ ⁺ ion is violated, and the low-frequency shift of the ν₁- and ν₃-stretching modes. The absence of absorption lines in the 1800–2400-cm⁻¹ region indicates that hydrogen bonding between the framework and the NH⁺ ₄ ion is very weak. The three-component splitting of the ν₄-bending mode indicates that the symmetry of NH⁺ ₄ ion is lower than C_3v. This implies that at least two N–H bonds of the NH⁺ ₄ ion are disturbed by hydrogen bonding. Computer analysis of the normal vibrations of the NH⁺ ₄ molecule for different symmetry types (using harmonic approximation) indicates that the best fit to the observed ν₄ triplet frequencies for C₁ symmetry implies a deviation of the valent angle ∠H–N–H from ideal T _d symmetry of around ±2.5°. The factors governing the behaviour of the NH⁺ ₄ ion in the analcime structure are discussed. The geometry of the nearest environment of the NH⁺ ₄ ion in the analcime structure is analyzed with respect to the present IR data. Received: 2 January 2002 / Accepted: 26 June 2002 Acknowledgements We thank Dr. D. Harlov and an anonymous reviewer for their helpful comments, as well as Dr. I.A. Belitsky and Dr. S.V. Goryainov for discussion of the material. This work is supported by RFBR grants 01-05-65414, 00-05-65305 and 02-05-65313.  相似文献   

Tululite,Ca14(Fe3+,Al)(Al,Zn,Fe3+,Si,P,Mn,Mg)15O36: a new Ca zincate-aluminate from combustion metamorphic marbles,central Jordan     

Hani N. Khoury  Ella V. Sokol  Svetlana N. Kokh  Yurii V. Seryotkin  Elena N. Nigmatulina  Sergei V. Goryainov  Elena V. Belogub  Ian D. Clark 《Mineralogy and Petrology》2016,110(1):125-140

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The Fe–C–O–H–N system at 6.3–7.8 GPa and 1200–1400 °C: implications for deep carbon and nitrogen cycles     

Alexander?G.?SokolEmail authorView author&#;s OrcID profile  Anatoly?A.?Tomilenko  Taras?A.?Bul’bak  Alexey?N.?Kruk  Pavel?A.?Zaikin  Ivan?A.?Sokol  Yurii?V.?Seryotkin  Yury?N.?Palyanov 《Contributions to Mineralogy and Petrology》2018,173(6):47

Interactions in a Fe–C–O–H–N system that controls the mobility of siderophile nitrogen and carbon in the Fe⁰-saturated upper mantle are investigated in experiments at 6.3–7.8 GPa and 1200–1400 °C. The results show that the γ-Fe and metal melt phases equilibrated with the fluid in a system unsaturated with carbon and nitrogen are stable at 1300 °C. The interactions of Fe₃C with an N-rich fluid in a graphite-saturated system produce the ε-Fe₃N phase (space group P6₃/mmc or P6₃22) at subsolidus conditions of 1200–1300 °C, while N-rich melts form at 1400 °C. At IW- and MMO-buffered hydrogen fugacity (fH₂), fluids vary from NH₃- to H₂O-rich compositions (NH₃/N₂?>?1 in all cases) with relatively high contents of alkanes. The fluid derived from N-poor samples contains less H₂O and more carbon which mainly reside in oxygenated hydrocarbons, i.e., alcohols and esters at MMO-buffered fH₂ and carboxylic acids at unbuffered fH₂ conditions. In unbuffered conditions, N₂ is the principal nitrogen host (NH₃/N₂?≤?0.1) in the fluid equilibrated with the metal phase. Relatively C- and N-rich fluids in equilibrium with the metal phase (γ-Fe, melt, or Fe₃N) are stable at the upper mantle pressures and temperatures. According to our estimates, the metal/fluid partition coefficient of nitrogen is higher than that of carbon. Thus, nitrogen has a greater affinity for iron than carbon. The general inference is that reduced fluids can successfully transport volatiles from the metal-saturated mantle to metal-free shallow mantle domains. However, nitrogen has a higher affinity for iron and selectively accumulates in the metal phase, while highly mobile carbon resides in the fluid phase. This may be a controlling mechanism of the deep carbon and nitrogen cycles.  相似文献   

Synthetic Gold Chalcogenides in the Au–Te–Se–S System and Their Natural Analogs     

Palyanova  G. A.  Tolstykh  N. D.  Zinina  V. Yu.  Kokh  K. A.  Seryotkin  Yu. V.  Bortnikov  N. S. 《Doklady Earth Sciences》2019,487(2):929-934

Doklady Earth Sciences - Quaternary chalcogenides of AuX (AuTe0.7Se0.2S0.1), Au3X10 (Au3Te6Se3S, Au3Te6Se2.5S1.5), and AuX2 (AuTe1.8Se0.2, AuTe1.8Se0.1S0.1) composition were synthesized for the...  相似文献   

Mineral inclusions in microdiamonds and macrodiamonds from kimberlites of Yakutia: a comparative study   总被引：10，自引：0，他引：10  

N.V. Sobolev  A.M. Logvinova  D.A. Zedgenizov  Y.V. Seryotkin  E.S. Yefimova  C. Floss  L.A. Taylor 《Lithos》2004,77(1-4):225-242

Chemical compositions were determined on mineral inclusions recovered from 290 microdiamonds (<1 mm) from 8 operating diamond mines in Yakutia. The sampled diamond mines include Mir, Udachnaya, Internatsionalnaya, Aykhal, Sytykanskaya, Yubileynaya, Komsomolskaya and Krasnopresnenskaya. The mineral inclusions include both ultramafic (peridotitic) suite (U-type) and eclogitic suite (E-type) examples. Olivines, chromites, Cr-pyropes, Cr-diopsides and enstatite were studied from U-type diamonds. Mg–Ca–Fe-garnets and omphacitic clinopyroxenes were studied from E-type microdiamonds. Abundances and compositions of these inclusions were compared with published and unpublished data on inclusions available from approximately 2000 macrodiamonds (>1 mm) from the same sources, and worldwide data for olivines and chromites. Although there are general similarities, notable exceptions were detected in about 10% of the inclusions from microdiamonds. For each of the pipes, anomalous compositions occur between the micro- and macrodiamond inclusions, but in different proportions, sometimes as high as 50% of the inclusions. Our study has demonstrated that mineral inclusions in microdiamonds are considerably more variable in their compositions and parageneses compared with inclusions in macrodiamonds.

Significant compositional anomalies in inclusions from microdiamonds include: (1) garnets containing pyroxene solid solution (majoritic component) both in U- and E-type microdiamonds from three pipes: Yubileynaya, Komsomolskaya and Krasnopresnenskaya. The moles of Si (pfu) in these garnets range from 3.07 to 3.13 and as high as 3.29, on the basis of 12 oxygens, along with a notable contents of Na₂O in two eclogitic garnets (0.43 and 0.93 wt.%) and uniquely high Cr₂O₃ and CaO contents in an ultramafic garnet of wehrlitic paragenesis; (2) coexisting wehrlitic garnets in a single microdiamond, one majoritic, the other normal, both with distinct +Eu anomalies, considered as signatures of crustal protoliths for the precursors to these garnets; (3) olivines with relatively low Fo (86–89) and high-NiO contents (0.46–0.64 wt.%), from Yubileynaya and Sytykanskaya microdiamonds; (4) chromites containing high-TiO₂ (up to 4.7 wt.%) and some extremely rich in MgO (Mg# 80). It is concluded that many of these compositional features observed may be related to a deeper origin for the microdiamond source region (>300 km), for at least a 10–30% portion of microdiamonds from each Yakutian pipe.  相似文献   

Sulfur–selenium isomorphous substitution and morphotropic transition in the Ag3Au(Se,S)2 series     

Yu.V. Seryotkin  G.A. Pal’yanova  N.E. Savva 《Russian Geology and Geophysics》2013,54(6):646-651

Gold–silver sulfoselenides of the series Ag3AuSexS2–x (x = 0.25; 0.5; 0.75; 1; 1.5) were synthesized from melts on heating stoichiometric mixtures of elementary substances in evacuated quartz ampoules. According to X-ray single-crystal analysis, compound Ag₃Au₁Se_0.5S_1.5 has the structure of gold–silver sulfide Ag3AuS2 (uytenbogaardtite) with space group R3c. The volume of this compound is 1.5% larger than that of the sulfide analog. According to powder X-ray diffraction, compounds Ag₃AuSe_0.25S_1.75 and Ag₃AuSe_0.75S_1.25 also show trigonal symmetry. Compounds Ag₃AuSeS and Ag₃AuSe_1.5S_0.5 are structurally similar to the low-temperature modification of gold–silver selenide Ag₃AuSe₂ (fischesserite) with space group I4132. These data suggest the existence of two solid solutions: petzite-type cubic Ag₃AuSe₂–Ag₃AuSeS (space group I4132) and trigonal Ag₃AuSe_0.75S_1.25–Ag₃AuS₂ (space group R3c).It was found that fischesserite from the Rodnikovoe deposit (southern Kamchatka) contains 3.5–4 wt.% S. At the Kupol deposit (Chukchi Peninsula), fischesserite contains up to 2.5 wt.% S and uytenbogaardtite contains up to 5.3 wt.% Se. At the Ol’cha and Svetloe (Okhotskoe) deposits (Magadan Region), uytenbogaardtite contains up to 0.5 and 1.8 wt.% Se, respectively. Literature data on the compositions of silver–gold selenides and sulfides from different deposits were summarized and analyzed. Analysis of available data on the S and Se contents of natural fischesserite and uytenbogaardtite confirms the miscibility gap near composition Ag3AuSeS.  相似文献   

Crystal structure of K-substituted gonnardite: separation of local water–cation assemblages     

Yurii V. Seryotkin  V. V. Bakakin 《Physics and Chemistry of Minerals》2014,41(3):173-180

K-substituted gonnardite, K_2.18Na_0.04Ca_0.02[Al_2.26Si_2.74O₁₀]·2.2H₂O, was studied by X-ray powder diffraction method. The structure was refined with the Rietveld technique in the tetragonal space group $I\overline{4} 2d$ with a = 13.65409(16), c = 6.56928(11) Å, V = 1224.74(2) ų, Z = 4. Most of K⁺ cations (1.94 apfu) statistically occupy three nearest positions to be considered as the split one. “Excess” cations are located in the position non-typical for K⁺. Statistics in the cation distribution is defined by the occupation of the additional position. Based on a crystal chemical positional model (C₂R₂A₂) [T₅O₁₀], the separation of the local water–cation assemblages from an average statistical pattern has been suggested.  相似文献