Order parameter and packing studies in nematic and smectic A phases by x‐ray diffraction

1988 ◽  
Vol 89 (5) ◽  
pp. 3317-3322 ◽  
Author(s):  
W. Haase ◽  
Z. X. Fan ◽  
H. J. Müller
Author(s):  
Gundula F Starkulla ◽  
Elisabeth Kapatsina ◽  
Angelika Baro ◽  
Frank Giesselmann ◽  
Stefan Tussetschläger ◽  
...  

Based on 5-(4-hydroxyphenyl)-2-octylpyrimidine 8, 5-phenylpyrimidine derivatives 3–7, 9 with different spacer chain lengths (C2 up to C6) and different terminal polar groups (Br, Cl, N3, OH, CN) were synthesized by etherification and nucleophilic substitution. The mesomorphic behaviour of these compounds was investigated by differential scanning calorimetry (DSC), polarizing optical microscopy (POM) and X-ray diffraction (WAXS and SAXS) and revealed smectic A mesophases for bromides, chlorides and azides 3, 4 and 6. For these compounds a maximum phase width was observed for the C5 spacer regardless of the terminal group, whereas the hydroxy- and cyano-substituted derivatives 5 and 7, respectively, were non mesomorphic and showed only melting transitions.


2002 ◽  
Vol 32 (2b) ◽  
pp. 495-500 ◽  
Author(s):  
E. L. Duarte ◽  
R. Itri ◽  
A. R. Sampaio ◽  
M. Simões ◽  
A. J. Palangana

2002 ◽  
Vol 91 (11) ◽  
pp. 9039-9042 ◽  
Author(s):  
J. H. Li ◽  
R. L. Forrest ◽  
S. C. Moss ◽  
Y. Zhang ◽  
A. Mascarenhas ◽  
...  

2011 ◽  
Vol 17 (3) ◽  
pp. 403-409 ◽  
Author(s):  
Karen L. Torres ◽  
Richard R. Vanfleet ◽  
Gregory B. Thompson

AbstractEight FePt thin film specimens of various thicknesses, compositions, and order parameters have been analyzed to determine the robustness and fidelity of multislice simulations in determining the chemical order parameter via electron diffraction (ED). The shape of the simulated curves depends significantly on the orientation and thickness of the specimen. The ED results are compared to kinematical scattering order parameters, from the same films, acquired from synchrotron X-ray diffraction (XRD). For the specimens analyzed with convergent beam electron diffraction conditions, the order parameter closely matched the order parameter as determined by the XRD methodology. However, the specimens analyzed by selected area electron diffraction conditions did not show good agreement. This has been attributed to substrate effects that hindered the ability to accurately quantify the intensity values of the superlattice and fundamental reflections.


1998 ◽  
Author(s):  
S. K. Giri ◽  
N. K. Pradham ◽  
R. Paul ◽  
S. Paul ◽  
P. Mandal ◽  
...  

2012 ◽  
Vol 05 ◽  
pp. 488-495 ◽  
Author(s):  
S. Izadi ◽  
Gh. Akbari ◽  
K. Janghorban ◽  
M. Ghaffari

In this study, mechanical alloying (MA) of Fe -50 Al , Fe -49.5 Al -1 B , and Fe -47.5 Al -5 B (at.%) alloy powders and mechanical properties of sintered products of the as-milled powders were investigated. X-ray diffraction (XRD) results showed the addition of B caused more crystallite refinement compared to the B -free powders. To consider the sintering and ordering behaviors of the parts produced from cold compaction of the powders milled for 80 h, sintering was conducted at various temperatures. It was found that the sintering temperature has no meaningful effect on the long-range order parameter. The transformation of the disordered solid solution developed by MA to ordered Fe - Al - ( B ) intermetallics was a consequence of sintering. Also, the nano-scale structure of the samples was retained even after sintering. The microhardness of pore-free zones of the nanostructured specimens decreased by increasing the sintering temperature. Moreover, the sintering temperature has no effect on the compressive yield stress. However, the fracture strain increased by increasing the sintering temperature. The samples containing 1 at.% B showed more strain to fracture compared with the B -free and 5 at.% B samples.


1993 ◽  
Vol 15 (3) ◽  
pp. 361-376 ◽  
Author(s):  
T. A. Lobko ◽  
B. I. Ostrovskii ◽  
A. I. Pavluchenko ◽  
S. N. Sulianov

1999 ◽  
Vol 583 ◽  
Author(s):  
S. Francoeur ◽  
G. A. Seryogin ◽  
S. A. Nikishin ◽  
H. Temkin

AbstractWe apply the technique of x-ray diffraction to the determination of the crystallographic structure and the quantitative measurement of the order parameter of ZnSnP2 epitaxial layers. In bulk, ZnSnP2 it is possible to obtain highly ordered distribution of Zn and Sn atoms in the cation sublattice, but epitaxial growth often produces partially ordered layers. The ordered and disordered phases correspond to the chalcopyrite and sphalerite structures and their respective band gaps are 1.66 and 1.24 eV. Since ZnSnP2 is almost lattice-matched to GaAs. it is interesting candidate for optoelectronic applications.Samples used in this work were grown by gas source molecular beam epitaxy on GaAs substrates. Slight variations in growth conditions could be induced to produce partially ordered and disordered structures. Chalcopyrite ordering is determined by the observation of several characteristic reflections identifying the lower symmetry of this structure. For example, reflections from (101), (217) and (611) planes, strictly forbidden for sphalerite, were measured. The quantitative determination of the order parameter could be made by comparing intensities of a carefully chosen set of measured and calculated reflections. We show that while kinematic approximation can be used to model weak superstructure reflections, in the calculation of the strong, low-angle, fundamental reflections used for intensity normalization it is necessary to take into account extinction effects. Order parameters varying from 0 to 30% were obtained.


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