Stresses in a plate with a periodic system of external parallel cracks in antisymmetric loading

1977 ◽  
Vol 13 (1) ◽  
pp. 105-107 ◽  
Author(s):  
M. P. Savruk
Author(s):  
J. Taft∅

It is well known that for reflections corresponding to large interplanar spacings (i.e., sin θ/λ small), the electron scattering amplitude, f, is sensitive to the ionicity and to the charge distribution around the atoms. We have used this in order to obtain information about the charge distribution in FeTi, which is a candidate for storage of hydrogen. Our goal is to study the changes in electron distribution in the presence of hydrogen, and also the ionicity of hydrogen in metals, but so far our study has been limited to pure FeTi. FeTi has the CsCl structure and thus Fe and Ti scatter with a phase difference of π into the 100-ref lections. Because Fe (Z = 26) is higher in the periodic system than Ti (Z = 22), an immediate “guess” would be that Fe has a larger scattering amplitude than Ti. However, relativistic Hartree-Fock calculations show that the opposite is the case for the 100-reflection. An explanation for this may be sought in the stronger localization of the d-electrons of the first row transition elements when moving to the right in the periodic table. The tabulated difference between fTi (100) and ffe (100) is small, however, and based on the values of the scattering amplitude for isolated atoms, the kinematical intensity of the 100-reflection is only 5.10-4 of the intensity of the 200-reflection.


1968 ◽  
Vol 14 (3) ◽  
pp. 331-339 ◽  
Author(s):  
E. D. Donets ◽  
V. A. Druin ◽  
V. L. Mikheev
Keyword(s):  

1970 ◽  
Vol 100 (1) ◽  
pp. 45-92 ◽  
Author(s):  
G.N. Flerov ◽  
V.A. Druin ◽  
A.A. Pleve

1986 ◽  
Vol 51 (11) ◽  
pp. 2582-2589 ◽  
Author(s):  
Antonín Lyčka ◽  
Jaroslav Holeček ◽  
Karel Handlíř ◽  
Josef Pola ◽  
Václav Chvalovský

The 17O, 13C, and 29Si NMR spectra of (CH3)3SiOC(O)R, CH3(XCH2)Si(OC(O)CH3)2, and R3GeOC(O)CH3 compounds are reported. In the 17O NMR spectra at 350 K the only signal is observed with the two latter series, but two well-resolved signals are displayed with the (CH3)3SiOC(O)R compounds. The equivalence of both oxygen atoms in carboxyl group on the NMR time scale is discussed from the viewpoint of a possible coordination of the oxygen atoms to the IVB group element of the periodic system.


2020 ◽  
Vol 53 (2) ◽  
pp. 1237-1242
Author(s):  
Mingzhou Yin ◽  
Andrea Iannelli ◽  
Mohammad Khosravi ◽  
Anilkumar Parsi ◽  
Roy S. Smith

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