scholarly journals Ballistic effectiveness of superdense solid composite propellants with zirconium or zirconium hydride

Author(s):  
D. Lempert ◽  
G. Manelis ◽  
G. Nechiporenko
Author(s):  
G.J.C. Carpenter

In zirconium-hydrogen alloys, rapid cooling from an elevated temperature causes precipitation of the face-centred tetragonal (fct) phase, γZrH, in the form of needles, parallel to the close-packed <1120>zr directions (1). With low hydrogen concentrations, the hydride solvus is sufficiently low that zirconium atom diffusion cannot occur. For example, with 6 μg/g hydrogen, the solvus temperature is approximately 370 K (2), at which only the hydrogen diffuses readily. Shears are therefore necessary to produce the crystallographic transformation from hexagonal close-packed (hep) zirconium to fct hydride.The simplest mechanism for the transformation is the passage of Shockley partial dislocations having Burgers vectors (b) of the type 1/3<0110> on every second (0001)Zr plane. If the partial dislocations are in the form of loops with the same b, the crosssection of a hydride precipitate will be as shown in fig.1. A consequence of this type of transformation is that a cumulative shear, S, is produced that leads to a strain field in the surrounding zirconium matrix, as illustrated in fig.2a.


1964 ◽  
Vol 25 (5) ◽  
pp. 451-453 ◽  
Author(s):  
S.W. Peterson ◽  
V.N. Sadana ◽  
W.L. Korst

2021 ◽  
Author(s):  
Anatoly G. KOREPIN ◽  
Natalia M. GLUSHAKOVA ◽  
David B. LEMPERT ◽  
Anatoly I. KAZAKOV ◽  
Gennady V. SHILOV ◽  
...  

Author(s):  
Xin Cui ◽  
wei huang ◽  
Lipeng Wu

Herein, by applying zirconium-hydride complex as the catalyst, the transfer hydrogenation of quinoline and indole derivatives with ammonia borane as the proton and hydride source is achieved. Up to 94%...


Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 39
Author(s):  
Lyudmila V. Parfenova ◽  
Pavel V. Kovyazin ◽  
Almira Kh. Bikmeeva ◽  
Eldar R. Palatov

The activity and chemoselectivity of the Cp2ZrCl2-XAlBui2 (X = H, Bui) and [Cp2ZrH2]2-ClAlEt2 catalytic systems activated by (Ph3C)[B(C6F5)4] or B(C6F5)3 were studied in reactions with 1-hexene. The activation of the systems by B(C6F5)3 resulted in the selective formation of head-to-tail alkene dimers in up to 93% yields. NMR studies of the reactions of Zr complexes with organoaluminum compounds (OACs) and boron activators showed the formation of Zr,Zr- and Zr,Al-hydride intermediates, for which diffusion coefficients, hydrodynamic radii, and volumes were estimated using the diffusion ordered spectroscopy DOSY. Bis-zirconium hydride clusters of type x[Cp2ZrH2∙Cp2ZrHCl∙ClAlR2]∙yRnAl(C6F5)3−n were found to be the key intermediates of alkene dimerization, whereas cationic Zr,Al-hydrides led to the formation of oligomers.


2018 ◽  
Vol 54 (45) ◽  
pp. 5724-5727 ◽  
Author(s):  
Zhongbao Jian ◽  
Constantin G. Daniliuc ◽  
Gerald Kehr ◽  
Gerhard Erker

Carbon monoxide reacts with zirconium hydride and methyl–B(6F5)2 to give a Zr-bound acetyl(hydrido)borate as the major product. This reacts further with CO to form a Zr-coordinated borata-β-lactone.


ChemInform ◽  
2001 ◽  
Vol 32 (15) ◽  
pp. no-no
Author(s):  
B. Tsuchiya ◽  
J. Huang ◽  
K. Konashi ◽  
W. Saiki ◽  
T. Onoue ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document