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1.
G. Barr A. L. Thorogood und W. L. Mloldawski 《Fresenius' Journal of Analytical Chemistry》1935,102(3-4):135
Ohne Zusammenfassung 相似文献
2.
G. Barr A. L. Thorogood W. L. Mloldawski 《Analytical and bioanalytical chemistry》1935,102(3-4):135-135
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Gordon J. Thorogood Brendan J. Kennedy Vanessa K. Peterson Vittorio Luca 《Journal of Physics and Chemistry of Solids》2011,72(6):692-700
The structure of the defect pyrochlore NaW2O6+δ·nH2−zO after ion exchange with K, Rb, Sr or Cs for Na has been investigated using thermal analysis, solid-state nuclear magnetic resonance, laboratory X-ray and neutron diffraction methods. Neutron diffraction studies show that both the A-type cations (Na+, K+, Rb+, and/or Cs+) and the water molecules reside within the channels that form in the 111 direction of the W2O6 framework and that these strongly interact. The analytical results suggest that the water and A-type cations compete for space in the tunnels within the W2O6 pyrochlore framework, with the total number of water molecules and cations being approximately constant in the six samples investigated. The interplay between the cations and water explains the non-linear dependence of the a lattice parameter on the choice of cation. It appears that the ion-exchange capacity of the material will be controlled by the amount of water initially present in the sample. 相似文献
4.
Rondahl Stina Holmgren Pointurier Fabien Ahlinder Linnea Ramebäck Henrik Marie Olivier Ravat Brice Delaunay François Young Emma Blagojevic Ned Hester James R. Thorogood Gordon Nelwamondo Aubrey N. Ntsoane Tshepo P. Roberts Sarah K. Holliday Kiel S. 《Journal of Radioanalytical and Nuclear Chemistry》2018,315(2):395-408
Journal of Radioanalytical and Nuclear Chemistry - This work presents the results for identification of chemical phases obtained by several laboratories as a part of an international nuclear... 相似文献
5.
Peter E. R. Blanchard Emily Reynolds Brendan J. Kennedy Chris D. Ling Zhaoming Zhang Gordon Thorogood Bruce C. C. Cowie Lars Thomsen 《Journal of synchrotron radiation》2014,21(6):1275-1281
Tc L3‐edge XANES spectra have been collected on powder samples of SrTcO3 (octahedral Tc4+) and NH4TcO4 (tetrahedral Tc7+) immobilized in an epoxy resin. Features in the Tc L3‐edge XANES spectra are compared with the pre‐edge feature of the Tc K‐edge as well as other 4d transition metal L3‐edges. Evidence of crystal field splitting is obvious in the Tc L3‐edge, which is sensitive to the coordination number and oxidation state of the Tc cation. The Tc L3 absorption edge energy difference between SrTcO3 (Tc4+) and NH4TcO4 (Tc7+) shows that the energy shift at the Tc L3‐edge is an effective tool for studying changes in the oxidation states of technetium compounds. The Tc L3‐edge spectra are compared with those obtained from Mo and Ru oxide standards with various oxidation states and coordination environments. Most importantly, fitting the Tc L3‐edge to component peaks can provide direct evidence of crystal field splitting that cannot be obtained from the Tc K‐edge. 相似文献
6.
Energy spectra for decaying 2D turbulence in a bounded domain 总被引:1,自引:0,他引:1
We use results derived in the framework of the replica approach to study the liquid-glass thermodynamic transition. The main results are derived without using replicas and applied to the study of the Lennard-Jones binary mixture introduced by Kob and Andersen. We find that there is a phase transition due to the entropy crisis. We compute both analytically and numerically the value of the phase transition point T(K) and the specific heat in the low temperature phase. 相似文献
7.
Rodriguez EE Poineau F Llobet A Kennedy BJ Avdeev M Thorogood GJ Carter ML Seshadri R Singh DJ Cheetham AK 《Physical review letters》2011,106(6):067201
We present evidence for possibly the highest magnetic ordering temperature in any compound without 3d transition elements. Neutron powder diffraction measurements, at both time-of-flight and constant wavelength sources, were performed on two independently prepared SrTcO3 powders. SrTcO3 adopts a distorted perovskite structure with G-type antiferromagnetic ordering and has a moment of 1.87(4)μB per Tc cation at room temperature with an extraordinarily high Néel point close to 750 °C. Electronic structure calculations reveal extensive mixing between the technetium 4d states and oxygen states proximal to the Fermi level. This hybridization leads to a close relationship between magnetic ordering temperature and moment formation in SrTcO3. 相似文献
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9.
Ceramics based on LnTiTaO6 (Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu) were prepared using a conventional solid-state ceramic route. The structure and microstructure of the samples were analyzed using scanning electron microscopy, synchrotron X-ray powder diffraction and neutron diffraction techniques. The unit cell volume of the ceramics decreased with a decrease in ionic radius of the rare-earth ions until a phase change was seen at Ho where the space group changed from Pnma to Pbcn. The results confirmed that the boundary of the aeschynite to euxenite phase change that lies between DyTiTaO6 and HoTiTaO6 and demonstrate that this is a result of distortion of the channels in the aeschynite structure. 相似文献
10.
Gordon J. Thorogood Brendan J. Kennedy Margaret M. Elcombe John V. Hanna 《Journal of solid state chemistry》2009,182(3):457-464
The structures of the defect pyrochlores AAl0.33W1.67O6 where A=K, Rb or Cs have been investigated using X-ray and neutron powder diffraction methods as well as the ab initio modelling program VASP. The three cubic pyrochlores exhibit a non-linear increase in lattice parameter with respect to ionic radius of the A cation as a consequence of displacive disorder of the A-type cations. Solid state 27Al MAS NMR studies of this pyrochlore system reveal shifts in the δ∼21-22 ppm range that are indicative of pseudo-5 coordinate Al environments and emanate from distorted Al octahedral with one abnormally long Al-O bond. Solid state 39K, 85Rb, 87Rb and 133Cs MAS and static NMR studies reflect the local cation disorder demonstrated in the structural studies. 相似文献