120 research outputs found
Influence of molecular weight on the phase behavior and structure formation of branched side-chain hairy-rod polyfluorene in bulk phase.
We report on an experimental study of the self-organization and phase behavior of hairy-rod Ď -conjugated branched side-chain polyfluorene, poly[9,9-bis(2-ethylhexyl)-fluorene-2,7-diyl]âi.e., poly[2,7â(9,9âbis(2âethylhexyl)fluorene] (PF2â6) âas a function of molecular weight (Mn) . The results have been compared to those of phenomenological theory. Samples for which Mn=3â147 kgâmol were used. First, the stiffness of PF2â6 , the assumption of the theory, has been probed by small-angle neutron scattering in solution. Thermogravimetry has been used to show that PF2â6 is thermally stable over the conditions studied. Second, the existence of nematic and hexagonal phases has been phenomenologically identified for lower and higher Mn (LMW, Mn<Mn* and HMW, Mn>Mn* ) regimes, respectively, based on free-energy argument of nematic and hexagonal hairy rods and found to correspond to the experimental x-ray diffraction (XRD) results for PF2â6 . By using the lattice parameters of PF2â6 as an experimental input, the nematic-hexagonal transition has been predicted in the vicinity of glassification temperature (Tg) of PF2â6 . Then, by taking the orientation parts of the free energies into account the nematic-hexagonal transition has been calculated as a function of temperature and Mn and a phase diagram has been formed. Below Tg of 80 °C only (frozen) nematic phase is observed for Mn<Mn*=104 gâmol and crystalline hexagonal phase for Mn>Mn* . The nematic-hexagonal transition upon heating is observed for the HMW regime depending weakly on Mn , being at 140â165 °C for Mn>Mn* . Third, the phase behavior and structure formation as a function of Mn have been probed using powder and fiber XRD and differential scanning calorimetry and reasonable semiquantitative agreement with theory has been found for MnâĽ3 kgâmol . Fourth, structural characteristics are widely discussed. The nematic phase of LMW materials has been observed to be denser than high-temperature nematic phase of HMW compounds. The hexagonal phase has been found to be paracrystalline in the (ab0) plane but a genuine crystal meridionally. We also find that all these materials including the shortest 10-mer possess the formerly observed rigid five-helix hairy-rod molecular structure
Surfactant induced mesomorphic behaviour of flexible polymers
Conditions for micro phase separated structures based on flexible polymers associated with surfactants have been investigated. Reasonably strong attractive interactions are required to oppose macro phase separation between polymer and surfactant. In order to obtain micro phase separation, additionally a sufficiently strong polar-nonpolar repulsion has to be present. Poly(4-vinyl pyridine), poly(2-vinyl pyridine) and polyamide 6 have been used as model polymers in this work. Associations based on protonation, metal coordination and hydrogen bonding are presented and shown to yield micro phase separation under suitable conditions. In the charged systems, the polar-nonpolar repulsion easily becomes large enough to render micro phase separated structures. In hydrogen bonded (i.e. noncharged) systems a more delicate balance can be achieved in which case an order-disorder transition takes place from a homogeneous state, exhibiting nonetheless a distinct SAXS peak due to characteristic block copolymer-like fluctuations, to a micro phase separated ordered state.</p
MESOMORPHIC STATE OF POLY(VINYLPYRIDINE)-DODECYLBENZENESULFONIC ACID COMPLEXES IN BULK AND IN XYLENE SOLUTION
Theoretically, lyotropic behavior of flexible polymers can be induced by associating the polymers with a large amount of long-tail surfactants leading to bottle-brush type conformations in suitable solvents. To address this and related questions, complexes of poly(2-vinylpyridine) (P2VP) and poly(4-vinylpyridine) (P4VP) with p-dodecylbenzenesulfonic acid (DBSA), characterized by FT-IR, were investigated in the bulk and in xylene, i.e., a good solvent for the alkyl side chains. At a 1:1 molar ratio of vinylpyridine monomer and DBS, the polymers are shown by FT-IR to be almost completely protonated. In the bulk, the complexes form mesomorphic layer structures which have been characterized by polarized optical microscopy and by both wide- and small-angle X-ray scattering. In the xylene solutions, birefringence indicating liquid crystallinity is observed for concentrations of the fully protonated P4VP-(DBSA)(1.0) complex of ca. 50% (w/w) and higher. In contrast, for P2VP(DBSA)(1.0), this is only observed at complex concentrations of ca. 70% (w/w) and higher. The mesomorphic behavior of P4VP(DBSA)(1.0) in xylene was further demonstrated by SAXS
Intermediate segregation type chain length dependence of the long period of lamellar microdomain structures of supramolecular comb-coil diblocks
A characteristic intermediate segregation type chain length dependence of the long period D of the lamellar microdomain structure of a class of comb-coil supramolecules is reported. The supramolecular comb-coil diblock copolymers studied consist of a polystyrene (PS) âcoilâ block and a âcombâ block of poly(4-vinylpyridine) (P4VP) either hydrogen bonded to pentadecyl phenol (PDP) (i.e., P4VP(PDP)-b-PS) or first protonated with methanesulfonic acid (MSA) and then hydrogen bonded to PDP (i.e., P4VP(MSA)(PDP)-b-PS). In both cases we find a scaling D ~ Ntotδ, δ â 0.8, where Ntot denotes the total number of monomers of the P4VP-b-PS backbone. In the case of diblock copolymers this would correspond to a characteristic intermediate segregation regime behavior. Pure PS-b-P4VP, on the other hand, shows the expected strong segregation behavior D ~ Ntotδ, δ â 0.7.
Determining collagen distribution in articular cartilage using contrast-enhanced micro-computed tomography
Objective: Collagen distribution within articular cartilage (AC) is typically evaluated from histological sections, e.g., using collagen staining and light microscopy (LM). Unfortunately, all techniques based on histological sections are time-consuming, destructive, and without extraordinary effort, limited to two dimensions. This study investigates whether phosphotungstic acid (PTA) and phosphomolybdic acid (PMA), two collagen-specific markers and X-ray absorbers, could (1) produce contrast for AC X-ray imaging or (2) be used to detect collagen distribution within AC. Method: We labeled equine AC samples with PTA or PMA and imaged them with micro-computed tomography (micro-CT) at pre-defined time points 0, 18, 36, 54, 72, 90, 180, 270 h during staining. The micro-CT image intensity was compared with collagen distributions obtained with a reference technique, i.e., Fourier-transform infrared imaging (FTIRI). The labeling time and contrast agent producing highest association (Pearson correlation, BlandeAltman analysis) between FTIRI collagen distribution and micro-CT -determined PTA distribution was selected for human AC. Results: Both, PTA and PMA labeling permitted visualization of AC features using micro-CT in non-calcified cartilage. After labeling the samples for 36 h in PTA, the spatial distribution of X-ray attenuation correlated highly with the collagen distribution determined by FTIRI in both equine (mean +/- S.D. of the Pearson correlation coefficients, r = 0.96 +/- 0.03, n = 12) and human AC (r = 0.82 +/- 0.15, n = 4). Conclusions: PTA-induced X-ray attenuation is a potential marker for non-destructive detection of AC collagen distributions in 3D. This approach opens new possibilities in development of non-destructive 3D histopathological techniques for characterization of OA. (C) 2015 The Authors. Published by Elsevier Ltd and Osteoarthritis Research Society International.Peer reviewe
Local structure study of In_xGa_(1-x)As semiconductor alloys using High Energy Synchrotron X-ray Diffraction
Nearest and higher neighbor distances as well as bond length distributions
(static and thermal) of the In_xGa_(1-x)As (0<x<1) semiconductor alloys have
been obtained from high real-space resolution atomic pair distribution
functions (PDFs). Using this structural information, we modeled the local
atomic displacements in In_xGa_(1-x)As alloys. From a supercell model based on
the Kirkwood potential, we obtained 3-D As and (In,Ga) ensemble averaged
probability distributions. This clearly shows that As atom displacements are
highly directional and can be represented as a combination of and
displacements. Examination of the Kirkwood model indicates that the standard
deviation (sigma) of the static disorder on the (In,Ga) sublattice is around
60% of the value on the As sublattice and the (In,Ga) atomic displacements are
much more isotropic than those on the As sublattice. The single crystal diffuse
scattering calculated from the Kirkwood model shows that atomic displacements
are most strongly correlated along directions.Comment: 10 pages, 12 figure
Polarized luminescence from self-assembled, aligned, and cleaved supramolecules of highly ordered rodlike polymers
Influence of molecular weight on the phase behavior and structure formation of branched side-chain hairy-rod polyfluorene in bulk phase
The chrystallinity of wood and the thickness of cellulose chrystallites in Norway spruce (Picea abies (L.) Karst.) investigated by x-ray diffraction
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