scholarly journals Reactivity of T-Nb2O5 or H-Nb2O5 towards V2O5. Synthesis in the solid state and properties of V4Nb18O55

2009 ◽  
Vol 7 (2) ◽  
pp. 222-227 ◽  
Author(s):  
Piotr Tabero ◽  
Elzbieta Filipek ◽  
Mateusz Piz
Keyword(s):  
Crystal Structure ◽  
Solid Solution ◽  
Solid State ◽  
Ir Spectra ◽  
Ir Spectrum ◽  
The Other ◽  
Other Hand ◽  
Structural Relations

AbstractThe IR spectrum of V4Nb18O55 has been compared with the IR spectra of selected niobates of known structures to show structural relations between these compounds. This comparison shows that V4Nb18O55 has crystal structure related to T-Nb2O5, W16Nb18O94 and Ba2NaNb5O15. On the other hand, reaction between V2O5 and H-Nb2O5 yields a solid solution of V2O5 in VNb9O25. It has been proposed two models of synthesized solid solution with formulas V1+xNb9-xO25 or V1+xNb9O25+5x/2.Independently of Nb2O5 polymorph, used for synthesis, the metastable compound VNbO5 cannot be synthesized in the solid state below 650°C

scholarly journals β-Li0.37Na0.63Fe(MoO4)2

2014 ◽  
Vol 70 (2) ◽  
pp. i9-i10 ◽  
Author(s):  
Amira Souilem ◽  
Mohamed Faouzi Zid ◽  
Ahmed Driss
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Solid State Reaction ◽  
Title Compound ◽  
General Position ◽  
Site Occupancy ◽  
The Other ◽  
Main Structure ◽  
Axis Direction ◽  
A Site

The title compound, lithium/sodium iron(III) bis[orthomolybdate(VI)], was obtained by a solid-state reaction. The main structure units are an FeO6octahedron, a distorted MoO6octahedron and an MoO4tetrahedron sharing corners. The crystal structure is composed of infinite double MoFeO11chains along theb-axis direction linked by corner-sharing to MoO4tetrahedra so as to form Fe2Mo3O19ribbons. The cohesion between ribbonsviamixed Mo—O—Fe bridges leads to layers arranged parallel to thebcplane. Adjacent layers are linked by corners shared between MoO4tetrahedra of one layer and FeO6octahedra of the other layer. The Na+and Li+ions partially occupy the same general position, with a site-occupancy ratio of 0.631 (9):0.369 (1). A comparison is made withAFe(MoO4)2(A= Li, Na, K and Cs) structures.

scholarly journals Determination of the Ratios of Ligands to Metal Ion of some Metal Complexes of Triazoles by Using Eleetronie Speetra in Organie Solvents

2004 ◽  
Vol 1 (1) ◽  
pp. 110-115
Author(s):  
Baghdad Science Journal
Keyword(s):  
Solid State ◽  
Metal Complexes ◽  
Electronic Spectra ◽  
Metal Ion ◽  
The Other ◽  
Molar Ratio ◽  
Other Hand

We found that 4,5- diphenyl- 3(2- propynyl) thio- 1??-triazole [1? forms a complex with Pd (11) ion of ratio 1:1 which absorbs light in CH2CI2 at 400 nm, and 4,5- diphenyl- 3(2- propenyl) thio- 1,2,4- triazole [II] forms complexes with Pd (II) ion of ratio 1:1 which absorbs light at 390 nm, and of ratio 2:1 which absorbs light at 435 nm. On the other hand, we found that the new derivative 4- phenyl- 5( p- amino phenyl) -3- mercapto- 1,2,4- triazole ?111? forms complexes with Cu (II) ion of the ratio 1:1 which absorbs light at 380 nm, with Ni (II) ion of the ratio 3:1 which absorbs light at 358 nm; and with Co (11) ion of the ratio 3.2:1 which absorbs light at 588 nm. The ratio of the complexes were determined by measuring the electronic spectra of the complexes in CH2G2 and (CH^NCHO at different concentrations ofthe ligands and f?xed ' •' of the metal ion in every case, then applying the molar ratio plots on the data. Our results were confirmed by precipitating most ofthe above complexes in solid state, and then each complex was analyzed elementally.

Microstructure and Hydrogen Permeability of Duplex Phase M-ZrNi (M=V, Nb, Ta) Alloys

2006 ◽  
Vol 980 ◽  
Author(s):  
Kazuhiro Ishikawa ◽  
Naoshi Kasagami ◽  
Tomoyuki Takano ◽  
Kiyoshi Aoki
Keyword(s):  
Crystal Structure ◽  
Solid Solution ◽  
High Performance ◽  
Gas Flow ◽  
Hydrogen Permeation ◽  
Hydrogen Permeability ◽  
The Other ◽  
Cast State ◽  
X Ray ◽  
Scanning Electron

AbstractIn order to develop non-Pd based high performance hydrogen permeation alloys, microstructure, crystal structure and hydrogen permeability of duplex phase M-ZrNi (M=V and Ta) alloys were investigated using a scanning electron microscope, an X-ray diffractometer and a gas flow meter. These results were compared with those of Nb-ZrNi ones which have been previously published. The hydrogen permeation was impossible in the V-ZrNi alloys, because they were brittle in the as-cast state. On the other hand, duplex phase alloys consisting of the bcc-(Ta, Zr) solid solution and the orthorhombic ZrNi (Cmcm) intermetallic compound were formed and hydrogen permeable in the Ta-ZrNi system. The Ta40Zr30Ni30 alloy shows the highest value of hydrogen permeability of 4.1×10-8 [molH2m-1s-1Pa-0.5] at 673 K, which is three times higher than that of pure Pd.

Anisotropic Microstructure and Hydrogen Permeability of Nb-Ti-Ni Duplex Phase Alloy Prepared by Hot Forging-Rolling Technique

2006 ◽  
Vol 980 ◽  
Author(s):  
Sho Tokui ◽  
Kazuhiro Ishikawa ◽  
Kiyoshi Aoki
Keyword(s):  
Solid Solution ◽  
Hydrogen Embrittlement ◽  
Hydrogen Permeability ◽  
Rolling Direction ◽  
Hot Forging ◽  
The Other ◽  
Rolling Reduction ◽  
Eutectic Microstructure ◽  
Ni Alloys ◽  
Other Hand

AbstractIt has been demonstrated that the as-cast Nb40Ti30Ni30 duplex phase alloy, which consists of the primary (Nb, Ti) solid solution and the fine lamellar type eutectic {TiNi+(Nb, Ti)} phase, shows higher hydrogen permeability ¶ than that of pure Pd without the hydrogen embrittlement at 673K. In this alloy, the eutectic phase contributes to the suppression of the hydrogen embrittlement, while the primary one does mainly to the hydrogen permeation. It is important to note that even if the eutectic microstructure disappears and is replaced by the small spherical (Nb, Ti) phase embedded in the TiNi matrix by rolling and subsequent annealing, its high hydrogen permeability and large resistance to the hydrogen embrittlement are sustained. Furthermore, the present authors have observed that the primary (Nb, Ti) phase is largely elongated along the rolling direction. Consequently, it is expected that rolled and annealed Nb-Ti-Ni alloys show the large anisotropy of the microstructure and the hydrogen permeability. In the present work, the microstructure and hydrogen permeability ¶nof the Nb40Ti30Ni30 alloy after rolling and annealing treatments are examined in order to develop highly hydrogen permeable alloys utilizing the anisotropic microstructure.The primary (Nb, Ti) phase and the very fine eutectic {TiNi+(Nb, Ti)} phase are observed in the as-cast Nb40Ti30Ni30 alloy by scanning electron microscopy (SEM). The X-ray diffractometry (XRD) indicates that this alloy consists of the B2-TiNi intermetallic compounds and the bcc- (Nb, Ti) solid solution. The primary (Nb, Ti) phase is largely elongated along the rolling direction by forging and subsequent rolling at 1173 K. On the other hand, the eutectic microstructure becomes unclear with increasing the rolling reduction. The composite alloys in which the (Nb, Ti) phase is elongated along to the rolling direction are obtained by 69 % rolling reduction. ¶n of this sample is four times higher than that of as-cast one. On the other hand, ¶ for the sample vertical to the rolling direction is reduced to about one third of that of as-cast one. Thus, the hydrogen permeability of the Nb40Ti30Ni30 alloy varies about ten times or more depending on the direction of the primary¡]Nb, Ti¡^ phase. We conclude that it is possible to produce highly hydrogen permeable Nb-Ti-Ni alloys using the anisotropy of the microstructure prepared by hot forging and rolling.

scholarly journals Effect of additional side groups on the vibrational frequencies of benzoquinone molecules

BIBECHANA ◽  
2016 ◽  
Vol 14 ◽  
pp. 66-76
Author(s):  
Nabin Kumar Raut ◽  
Hari Prasad Lamichhane
Keyword(s):  
Ir Spectra ◽  
Gas Phase ◽  
Vibrational Frequencies ◽  
The Other ◽  
Methyl Groups ◽  
Computational Investigation ◽  
Strongly Coupled ◽  
Solvent Phase ◽  
Other Hand

The present work enumerates detailed computational investigation into the IR spectra in gas phase and in solvent of 1, 4- Benzoquinone family (benzoquinone (BQ), duroquinone (DQ), plastoquinone (PQ), ubiquinone (UQ), and dimethoxy dimethyl benzoquinone (MQo)). In  the spectra of BQ, PQ, and DQ, we observed separate intense carbonyl (C=O) and C=C bands respectively around 1730 cm-1 (intense), 1645 cm-1 (weak). On the other hand, for UQ and MQo, three prominent bands around 1652, 1703, and 1733 cm-1 were observed, where two C=O modes were uncoupled but one of the carbonyl is strongly coupled with C=C vibrations. The additional methyl groups downshift the intense carbonyl bands and upshift C=C mode frequencies. The carbonyl modes further downshifted in the solvent phase calculation.BIBECHANA 14 (2017) 66-76

scholarly journals Crystal structure of the co-crystalline adduct 1,3,6,8-tetraazatricyclo[4.4.1.13,8]dodecane (TATD)–4-bromophenol (1/2)

2015 ◽  
Vol 71 (5) ◽  
pp. 463-465 ◽  
Author(s):  
Augusto Rivera ◽  
Juan Manuel Uribe ◽  
Jicli José Rojas ◽  
Jaime Ríos-Motta ◽  
Michael Bolte
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Hydrogen Bonds ◽  
Rotation Axis ◽  
The Other ◽  
Two Dimensional ◽  
Asymmetric Unit ◽  
Species Association ◽  
Crystalline Adduct ◽  
Aminal Cage

The structure of the 1:2 co-crystalline adduct C8H16N4·2C6H5BrO, (I), from the solid-state reaction of 1,3,6,8-tetraazatricyclo[4.4.1.13,8]dodecane (TATD) and 4-bromophenol, has been determined. The asymmetric unit of the title co-crystalline adduct comprises a half molecule of aminal cage polyamine plus a 4-bromophenol molecule. A twofold rotation axis generates the other half of the adduct. The primary inter-species association in the title compound is through two intermolecular O—H...N hydrogen bonds. In the crystal, the adducts are linked by weak non-conventional C—H...O and C—H...Br hydrogen bonds, giving a two-dimensional supramolecular structure parallel to thebcplane.

Effect of Temperature on the Structural and Magnetic Properties of Co0.7Zn0.3Fe2O4 Ceramic Prepared from Solid State Reaction

2015 ◽  
Vol 804 ◽  
pp. 38-41
Author(s):  
Pattarinee Klumdoung ◽  
Piyapong Pankaew
Keyword(s):  
Crystal Structure ◽  
Solid Solution ◽  
Magnetic Properties ◽  
Solid State ◽  
Solid State Reaction ◽  
Sintering Temperature ◽  
Effect Of Temperature ◽  
Dense Structure ◽  
Paramagnetic Behavior ◽  
Structural And Magnetic Properties

In present study, the Co0.7Zn0.3Fe2O4 ceramic was prepared using solid state reaction. The crystal structure of prepared ceramic indicated as solid solution. The SEM result indicated the dense structure of prepared ceramic as increased sintering temperature. For VSM result of Co0.7Zn0.3Fe2O4 ceramic indicated the super paramagnetic behavior with high magnetization. These results could lead us to the development of Co0.7Zn0.3Fe2O4 ceramic preparation optimized for specific applications.

FT-IR Spectroscopic Study of 1,5-Pentanedithiol and 1,6-Hexanedithiol Adsorbed on NaA, CaA and NaY Zeolites

2005 ◽  
Vol 60 (8-9) ◽  
pp. 633-636 ◽  
Author(s):  
Nuri Öztürk ◽  
Çağrı Çırak ◽  
Semiha Bahçeli
Keyword(s):  
Infrared Spectroscopy ◽  
Ir Spectra ◽  
Spectroscopic Study ◽  
The Other ◽  
Other Hand ◽  
Liquid Phases ◽  
Stretching Vibration ◽  
Ft Ir ◽  
Ir Spectroscopic ◽  
Nay Zeolites

The adsorption of 1,5-pentanedithiol (1,5-PDT) and 1,6-hexanedithiol (1,6-HDT) in liquid phases on NaA (or 4A-type), CaA (or 5A-type) and NaY zeolites has been studied by using infrared spectroscopy. From the IR spectra it is found that the peak positions of the symmetric as well as the antisymmetric modes of the methylene (CH2) groups are observed at almost the same band values for the title dithiolates adsorbed on the A-type and NaY zeolites. On the other hand, the weak SH stretching vibration, observed for all samples, can be attributed to the sulphure atoms of 1,5-PDT and 1,6-HDT coordinatively adsorbed on cationic sites of the zeolites.

Tris [(trimethylsilyl)oxy] antimony

1994 ◽  
Vol 49 (7) ◽  
pp. 855-858 ◽  
Author(s):  
Michael Baier ◽  
Klaus Angermaier ◽  
Hubert Schmidbaur
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Gas Phase ◽  
Structure Determination ◽  
Spectroscopic Data ◽  
Mass Spectrometric ◽  
Unit Cell ◽  
The Other ◽  
X Ray ◽  
Trigonal Bipyramidal

Abstract Tris[(trimethylsilyl)oxy]antimony (Sb(OSiMe3)3, 1) has been prepared from SbCl3 and 3 equiv. of LiOSiMe3 in diethylether. According to mass spectrometric and NMR spectroscopic data, 1 appears to be a monomer in solution and in the gas phase. Dimerisation occurs, however, in the solid state as verified by an X-ray crystal structure determination. The unit cell contains three crystallographically independent monomers, two of which form one type of dimer, while the other is part of a centrosymmetrical dimer. In both types of dimers two Sb atoms are connected via two OSiMe3 groups to form distorted Sb2O2-squares. Together with the remaining 4 OSiMe3 groups and the two stereochemically active lone pairs, each Sb exhibits a trigonal bipyramidal coordination.

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