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Oriented Samples (oriented + sample)
Selected AbstractsGrowth of lead bromide polycrystalline filmsCRYSTAL RESEARCH AND TECHNOLOGY, Issue 10 2004M. Giles Abstract Lead bromide polycrystalline films were grown by the physical vapor deposition method (PVD). Glass 1,x1, in size, uncoated, and coated with Indium Tin Oxide (ITO), was used as substrate and rear contact. The starting material was evaporated at temperatures from 395°C to 530°C under high vacuum atmosphere (6 x 10 -3 Pa) and during 8 days. The substrate temperature was prefixed from 190°C to 220°C. Film thickness yielded values from 40 to 90 ,m. Optical microscopy and scanning electron microscopy (SEM) were performed on the films. Grain size resulted to be from 1.0 to 3.5 ,m. SEM and X-ray diffraction indicate that films grow with a preferred orientation with the (0 0 l) planes parallel to the substrate. The Texture Coefficient (TC) related to the plane (0 0 6) was 7.3. Resistivity values in the order of 1012 ,cm were obtained for the oriented samples, but a strong polarization indicates severe charge transport problems in the films. Film properties were correlated with the growth temperature and with previous results for films of other halides. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Morphology and texture development of uniaxially stretched poly(ethylene naphthalene-2,6-dicarboxylate)JOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007A. Douillard Abstract The texture development of PEN films with different semicrystalline morphologies have been studied by X-ray diffraction. These different structures have been obtained by uniaxially stretching PEN amorphous films at 100 and 160°C (below and above Tg) at different drawing ratios. Samples have also been characterized by DSC to determine the crystallinity ratios, the crystallization, and melting temperatures. To define the orientation of crystallites in the oriented samples, pole figures have been constructed, as a function of temperature and drawing ratio (DR) in the range 1.5,4. In the range from DR = 2 to 4 the orientation is clearly uniplanar-axial. At Tdraw = 100°C the crystallinity shown by DSC analysis is higher than the sample stretched at 160°C. The orientation is also higher when samples are stretched at 100°C. The naphthalene rings mainly stay in the plane of the film with a lower fraction perpendicular to the plane of the film. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 395,401, 2007 [source] Microstructural effects on hot drawing syndiotactic styrene P-methyl styrene copolymerPOLYMER ENGINEERING & SCIENCE, Issue 10 2001R. J. Yan Crystalline syndiotactic styrene/p-methyl styrene copolymer (SPMS) has been oriented by tensile drawing at various temperatures between the glass transition and crystalline melting point. The microstructural changes resulting from drawing have been studied using differential scanning calorimetry (DSC) and wide angle X-ray diffraction (WAXD). WIth increasing draw temperature, both melting temperature and crystalline dimensions of the oriented samples increase. The heat of fusion increases with increasing draw temperature up to ,200°C. It also increases with draw ratio and draw rate, while the crystalline width increases only with draw ratio. THe amorphous fraction shows a clear glass transition, the temperature of which (Tg) increases with draw ratio. However, Tg decreases somewhat with increasing draw temperature. This is interpreted in terms of the stretching of the randomly coiled amorphous phase molecules. [source] 4-Fluorophenylglycine as a Label for 19F NMR Structure Analysis of Membrane-Associated PeptidesCHEMBIOCHEM, Issue 11 2003Sergii Afonin Abstract The non-natural amino acid 4-fluorophenylglycine (4F-Phg) was incorporated into several representative membrane-associated peptides for dual purpose. The 19F-substituted ring is directly attached to the peptide backbone, so it not only provides a well-defined label for highly sensitive 19F NMR studies but, in addition, the D and L enantiomers of the stiff side chain may serve as reporter groups on the transient peptide conformation during the biological function. Besides peptide synthesis, which is accompanied by racemisation of 4F-Phg, we also describe separation of the epimers by HPLC and removal of trifluoroacetic acid. As a first example, 18 different analogues of the fusogenic peptide "B18" were prepared and tested for induction of vesicle fusion; the results confirmed that hydrophobic sites tolerated 4F-Phg labelling. Similar fusion activities within each pair of epimers suggest that the peptide is less structured in the fusogenic transition state than in the helical ground state. In a second example, five doubly labelled analogues of the antimicrobial peptide gramicidin S were compared by using bacterial growth inhibition assays. This cyclic ,-sheet peptide could accommodate both L and D substituents on its hydrophobic face. As a third example, we tested six analogues of the antimicrobial peptide PGLa. The presence of d- 4F-Phg reduced the biological activity of the peptide by interfering with its amphiphilic ,-helical fold. Finally, to illustrate the numerous uses of l- 4F-Phg in 19F NMR spectroscopy, we characterised the interaction of labelled PGLa with uncharged and negatively charged membranes. Observing the signal of the free peptide in an aqueous suspension of unilamellar vesicles, we found a linear saturation behaviour that was dominated by electrostatic attraction of the cationic PGLa. Once the peptide is bound to the membrane, however, solid-state 19F NMR spectroscopy of macroscopically oriented samples revealed that the charge density has virtually no further influence on the structure, alignment or mobility of the peptide. [source] | ||||||||||