scholarly journals Effect of tungsten disulfide nanotubes on crystallization of polylactide under uniaxial deformation and annealing

2021 ◽  
Vol 2 (1) ◽  
Author(s):  
Fausta Loffredo ◽  
Loredana Tammaro ◽  
Tiziana Di Luccio ◽  
Carmela Borriello ◽  
Fulvia Villani ◽  
...  
Keyword(s):  
Biomedical Applications ◽  
Structural Evolution ◽  
Tungsten Disulfide ◽  
Fine Tuning ◽  
Nanocomposite Films ◽  
Uniaxial Deformation ◽  
Scanning Calorimetry ◽  
X Ray ◽  
X Ray Scattering

AbstractTungsten disulfide (WS2) nanotubes (NTs) are examined here as a filler for polylactide (PLA) for their ability to accelerate PLA crystallization and for their promising biocompatibility in relevant to biomedical applications of PLA-WS2 nanocomposites. In this work, we have studied the structural and thermal properties of PLA-WS2 nanocomposite films varying the concentration of WS2 NTs from 0 (neat PLA) to 0.6 wt%. The films were uniaxially drawn at 90 °C and annealed at the same temperature for 3 and 10 min. Using wide angle x-ray scattering, Raman spectroscopy and differential scanning calorimetry, we probed the effects of WS2 NT addition on the structure of the PLA films at various stages of processing (unstretched, stretching, annealing). We found that 0.6 wt% of WS2 induces the same level of crystallinity in as stretched PLA-WS2 as annealing in neat PLA for 10 min. These data provide useful insights into the role of WS2 NTs on the structural evolution of PLA-WS2 composites under uniaxial deformation, and extend their applicability to situations where fine tuning of PLA crystallinity is desirable.

scholarly journals Structural Evolution of LLDPE-LMW/HMW Blend during Uniaxial Deformation as Revealed by In Situ Synchrotron Radiation X-ray Scattering

2020 ◽  
Vol 39 (1) ◽  
pp. 102-112
Author(s):  
Pin-Zhang Chen ◽  
Hao-Yuan Zhao ◽  
Zhi-Jie Xia ◽  
Qian-Lei Zhang ◽  
Dao-Liang Wang ◽  
...  
Keyword(s):  
Synchrotron Radiation ◽  
Structural Evolution ◽  
Uniaxial Deformation ◽  
X Ray ◽  
X Ray Scattering ◽  
Ray Scattering

scholarly journals Interaction of Poly L-Lactide and Tungsten Disulfide Nanotubes Studied by in Situ X-ray Scattering during Expansion of PLLA/WS2NT Nanocomposite Tubes

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1764
Author(s):  
Lison Rocher ◽  
Andrew S. Ylitalo ◽  
Tiziana Di Luccio ◽  
Riccardo Miscioscia ◽  
Giovanni De Filippo ◽  
...  
Keyword(s):  
Extrusion Direction ◽  
Tungsten Disulfide ◽  
Molding Process ◽  
X Ray ◽  
X Ray Scattering ◽  
Polymer Crystals ◽  
Neat Plla ◽  
Tube Expansion ◽  
Ray Scattering

In situ synchrotron X-ray scattering was used to reveal the transient microstructure of poly(L-lactide) (PLLA)/tungsten disulfide inorganic nanotubes (WS2NTs) nanocomposites. This microstructure is formed during the blow molding process (“tube expansion”) of an extruded polymer tube, an important step in the manufacturing of PLLA-based bioresorbable vascular scaffolds (BVS). A fundamental understanding of how such a microstructure develops during processing is relevant to two unmet needs in PLLA-based BVS: increasing strength to enable thinner devices and improving radiopacity to enable imaging during implantation. Here, we focus on how the flow generated during tube expansion affects the orientation of the WS2NTs and the formation of polymer crystals by comparing neat PLLA and nanocomposite tubes under different expansion conditions. Surprisingly, the WS2NTs remain oriented along the extrusion direction despite significant strain in the transverse direction while the PLLA crystals (c-axis) form along the circumferential direction of the tube. Although WS2NTs promote the nucleation of PLLA crystals in nanocomposite tubes, crystallization proceeds with largely the same orientation as in neat PLLA tubes. We suggest that the reason for the unusual independence of the orientations of the nanotubes and polymer crystals stems from the favorable interaction between PLLA and WS2NTs. This favorable interaction leads WS2NTs to disperse well in PLLA and strongly orient along the axis of the PLLA tube during extrusion. As a consequence, the nanotubes are aligned orthogonally to the circumferential stretching direction, which appears to decouple the orientations of PLLA crystals and WS2NTs.

scholarly journals Resonant Inelastic X-ray Scattering on Ferrous and Ferric Bis-imidazole Porphyrin and Cytochromec: Nature and Role of the Axial Methionine–Fe Bond

2014 ◽  
Vol 136 (52) ◽  
pp. 18087-18099 ◽  
Author(s):  
Thomas Kroll ◽  
Ryan G. Hadt ◽  
Samuel A. Wilson ◽  
Marcus Lundberg ◽  
James J. Yan ◽  
...  
Keyword(s):  
X Ray ◽  
X Ray Scattering ◽  
Ray Scattering

scholarly journals Prominent role of oxygen in the multiferroicity ofDyMnO3andTbMnO3: A resonant soft x-ray scattering spectroscopy study

2016 ◽  
Vol 94 (3) ◽  
Author(s):  
S. W. Huang ◽  
J. M. Lee ◽  
Horng-Tay Jeng ◽  
YuCheng Shao ◽  
L. Andrew Wray ◽  
...  
Keyword(s):  
Spectroscopy Study ◽  
X Ray ◽  
X Ray Scattering ◽  
Ray Scattering

Thermotropic behavior of sodium cholesteryl carbonate

2009 ◽  
Vol 24 (1) ◽  
pp. 156-163 ◽  
Author(s):  
Rabkwan Chuealee ◽  
Timothy S. Wiedmann ◽  
Teerapol Srichana
Keyword(s):  
Phase Behavior ◽  
Chemical Structure ◽  
Liquid Crystalline ◽  
Polarized Light ◽  
Wave Number ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
X Ray Scattering ◽  
C Nmr

Sodium cholesteryl carbonate ester (SCC) was synthesized, and its phase behavior was studied. The chemical structure was assessed by solid-state infrared spectroscopy based on vibration analysis. The wave number at 1705 and 1276 cm−1 corresponds to a carbonyl carbonate and O–C–O stretching of SCC, respectively. Molecular structure of SCC was further investigated with 1H and 13C NMR spectroscopy. The chemical shift, for the carbonyl carbonate resonance appeared at 155.5 ppm. A molecular mass of SCC was at m/z of 452. Differential scanning calorimetry (DSC), video-enhanced microscopy (VEM) together with polarized light microscopy, and small-angle x-ray scattering (SAXS) were used to characterize the phase behavior as a function of temperature of SCC. Liquid crystalline phase was formed with SCC. Based on the thermal properties and x-ray diffraction, it appears that SCC forms a structure analogous to the type II monolayer structure observed with cholesterol esters.

Morphological basis for the complex melting behaviour of isotactic polystyrene

e-Polymers ◽  
2002 ◽  
Vol 2 (1) ◽  
Author(s):  
Mahmoud Al-Hussein ◽  
Gert Strobl
Keyword(s):  
Morphological Changes ◽  
Melting Behaviour ◽  
Temperature Dependent ◽  
Molten Material ◽  
Scanning Calorimetry ◽  
Isotactic Polystyrene ◽  
X Ray ◽  
Long Period ◽  
X Ray Scattering ◽  
Increasing Temperature

AbstractTemperature-dependent small-angle X-ray scattering spectroscopy of isothermally cold crystallized isotactic polystyrene revealed considerable morphological reorganization during subsequent heating to the melt. Both the crystalline thickness and the long period increased continuously with increasing temperature before the samples finally melted. The temperature dependence of these changes correlated very well with the melting behaviour observed with differential scanning calorimetry. As the temperature increased during a heating scan, the initial lamellae that formed during isothermal crystallization showed only little reorganization until they started to melt. Then, the molten material recrystallized continuously into increasingly thicker lamellae at increasing temperature until they finally melted. As the crystallization temperature approached the final melting temperature of the recrystallized lamellae, the initial lamellae melted without further recrystallization and no morphological changes were seen in this case.

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