A Mechanical Loading/Synchrotron X-Ray Diffraction System for In-Situ Determination of Lattice Strains

2005 ◽  
Author(s):  
Matthew Miller ◽  
Paul Dawson
CrystEngComm ◽  
2019 ◽  
Vol 21 (1) ◽  
pp. 41-52 ◽  
Author(s):  
Siriyara Jagannatha Prathapa ◽  
Cara Slabbert ◽  
Manuel A. Fernandes ◽  
Andreas Lemmerer

In situ cryocrystallisation enabled the crystal structure determination of a homologous series of low-melting n-alkyl methyl esters Cn−1H2n+1CO2CH3.


2014 ◽  
Vol 904 ◽  
pp. 150-154
Author(s):  
Zhe Wei Yang ◽  
Xin Fan ◽  
Li Ang Guo ◽  
Wei Ting Wei

The graphene oxide/Fe3O4 composites were prepared by in situ precipitation method in this article. The microstructure and surface morphology of composites were characterized by Fourier transform infrared spectrum, X-ray diffraction and scanning electron microscopy, respectively. Cyclic voltammetry was employed for the determination of specific capacitance and other electrochemical performances. It was shown that there was the chemical bonding force between GO and Fe3O4 particles. And the surfaces of GO were wrapped by the Fe3O4 particles precipitated on the surfaces of GO sheets and no impurities were detected. Furthermore, the specific capacitance of GO/Fe3O4 composite electrodes decreased as Fe3O4 particles reduced and the redox peaks became weaker owing to the addition of nonconductive Fe3O4 particles.


1999 ◽  
Vol 82 (9) ◽  
pp. 2566-2568 ◽  
Author(s):  
Alessandro F. Gualtieri ◽  
Edoardo Mazzucato ◽  
Paolo Venturelli ◽  
Alberto Viani ◽  
Paolo Zannini ◽  
...  

2008 ◽  
Vol 2008 (27) ◽  
pp. 253-260
Author(s):  
Y. Kuru ◽  
M. Wohlschlögel ◽  
U. Welzel ◽  
E. J. Mittemeijer
Keyword(s):  

2013 ◽  
Vol 21 (3) ◽  
pp. 7-7
Author(s):  
Charles Lyman

Many researchers view microanalysis as the determination of composition and structure of individual phases at a spatial resolution of 1 μm or better. It is remarkable to me that much of what we know about the phases shown in equilibrium phase diagrams was determined using bulk analysis techniques like powder X-ray diffraction in combination with light microscopy of flat-polished sections of materials. The identities and amounts of phases were deduced from systematic experiments because there was no way to analyze micrometer-sized phases in situ.


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