scholarly journals Characterization of toluene and 2-methylnaphthalene transport separated by syndiotactic polystyrene having various crystalline forms

2013 ◽  
Vol 45 (11) ◽  
pp. 1135-1139 ◽  
Author(s):  
Koichiro Tanigami ◽  
Daisuke Ishii ◽  
Takahiko Nakaoki ◽  
Pieter Stroeve
2006 ◽  
Vol 39 (21) ◽  
pp. 7199-7203 ◽  
Author(s):  
P. Govindaiah ◽  
S. R. Mallikarjuna ◽  
C. Ramesh

Polyhedron ◽  
2009 ◽  
Vol 28 (4) ◽  
pp. 835-843 ◽  
Author(s):  
Manju Rajeswaran ◽  
Thomas N. Blanton ◽  
Ching W. Tang ◽  
William C. Lenhart ◽  
Steven C. Switalski ◽  
...  

1999 ◽  
Vol 14 (6) ◽  
pp. 2644-2654 ◽  
Author(s):  
F. Rajabalee ◽  
V. Métivaud ◽  
D. Mondieig ◽  
Y. Haget ◽  
M. A. Cuevas-Diarte

X-ray diffraction analyses of the pure components n-tricosane and n-pentacosane and of their binary mixed samples have enabled us to characterize the crystalline phases observed at “low temperature.” Contrary to what was announced in literature on the structural behavior of mixed samples in odd-odd binary systems with Δn = 2, the three domains are not all orthorhombic. This work has enabled us to show that two of the domains are, in fact, monoclinic (Aa, Z = 4), and the other one is orthorhombic (Pca21, Z = 4). The conclusions drawn in this work can easily be transposed to other binary systems of n-alkanes.


2015 ◽  
Vol 71 (4) ◽  
pp. 819-828 ◽  
Author(s):  
A. Valmas ◽  
K. Magiouf ◽  
S. Fili ◽  
M. Norrman ◽  
G. Schluckebier ◽  
...  

The primary focus of the present work is the study of the effects that two ligands and the crystallization pH have on the crystalline forms of human insulin. For this purpose, human insulin (HI) was co-crystallized with two distinct phenolic derivatives: the organic ligandsmeta-cresol (m-cresol) and 4-nitrophenol. The formation of polycrystalline precipitates was then followed by means of structural characterization of the individual specimens in terms of unit-cell symmetry and parameters. In both cases, two different polymorphs were identifiedviaX-ray powder diffraction measurements, the first of hexagonal symmetry (R3 space group) at higher pH values and the second of monoclinic symmetry (space groupP21) with unit-cell parametersa= 87.4282 (5),b = 70.5020 (3),c= 48.3180 (4) Å, β = 106.8958 (4)°, the latter of which to our knowledge has never been observed before.


2002 ◽  
Vol 85 (10) ◽  
pp. 2084-2091 ◽  
Author(s):  
Won-Mook Choi ◽  
Cheon-Il Park ◽  
O Ok Park ◽  
Jae-Gon Lim

Author(s):  
J. Bentley ◽  
L. J. Romana ◽  
L. L. Horton ◽  
C. J. McHargue

As part of extensive fundamental studies of ion-implanted ceramics, analytical electron microscopy (AEM) has been used to characterize [0001] single crystal 6H α-silicon carbide implanted at room temperature with 160 keV 57Fe ions to fluences of 1,3, and 6 x 1016 ions/cm2. AEM was performed at 100 kV with a Philips EM400T equipped with a field emission gun, a 6585 STEM unit, an EDAX 9100/70 energy dispersive X-ray spectrometer (EDS), and a Gatan 666 parallel-detection electron energy loss spectrometer (PEELS).A micrograph of a cross-sectioned specimen implanted with 6 × 1016 ions/cm2 is shown in Fig. 1. The implanted region extending to 195 nm from the surface is amorphous, as confirmed by convergent beam electron diffraction (CBED) patterns (insets), and contains iron at levels easily detectable by EDS (Fig. 2). The 15 nm lattice fringes of the edge-on 6H basal planes in the substrate provide an unambiguous depth calibration scale. The transition layer at the end of the ion range exhibits the expected strain contrast. The depth profile of the implanted iron was measured by EDS line scans perpendicular to the implant surface; the mean of three of these scans is shown by the filled symbols in Fig. 3. The integrated iron profile agrees with the expected 6.0 × 1016 ions/cm2 only if the density of the amorphous SiC is equal to that of its crystalline forms, rather than the 20% lower density reported earlier.


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