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  • 1
    ISSN: 1573-0581
    Schlagwort(e): Structure ; morphology ; petrology ; peridotite-basalt
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie , Physik
    Notizen: Abstract The St. Paul F.Z. is a large structural domain made up of multiple transform faults interrupted by several Intra-Transform Ridge (ITR) spreading segments. Two regions were studied in details by submersible: (1) The ITR short (〈20 km in length) segment near 0° 37′N–25° 27′W and 1° N–27° 42′W and (2) The St. Peter and St. Paul's Rocks (SPPR) massif located at 29° 25′W (¡3700 m depth). (1) The short ITR segments consist of a magma starved rift valley with recent volcanic activities at 4700 m depth. A geological profile made along the rift valley wall showed localized volcanics (basalts and dykes) which are believed to overlay and intrude the ultramafics. The geological setting and the high ultramafic/volcanic ratio suggest an extremely low magmatic supply and crustal-mantle uplift during lithospheric stretching and denudation. (2) The St. Peter and St. Paul's Rocks (SPPR) massif consists of a sigmoidal ridge within the active transform zone. The SPPR is divided into two different geological domains called the North and the South Ridges. The North Ridge consists of strongly tectonized fault scarps composed of banded and mylonitized peridotite, sporadic gabbros (3900–2500 m) and metabasalts (2700–1700 m). The South Ridge is less tectonized with undeformed, serpentinized spinel lherzolite (2000–1400 m) and basalts. Extensional motion and denudation accompanied by diapirism affected the South Ridge within a transform domain. Instead, the North Ridge was formed during an important strike-slip and faulting motion resulting in the uplifted portion of the St. Paul F.Z. transverse ridge. There is a regional compositional variation of the volcanics where E-MORBs and alkali basalts are produced on the SPPR massif and are comparable to the adjacent northern segments of the Mid-Atlantic Ridge. On the other hand, N and T- MORBs collected from the eastern part of the St. Paul F.Z. (25° 27′ W IRT) are similar to the volcanics from the southern segments of the MAR. The peridotites exposed in these provinces (SPPR and ITR) are similar in their REE and trace element distribution. Different degrees (3–15%) of partial melting of a mixed composite mantle consisting of spinel and amphibole bearing lherzolite veined with 5–40% clinopyroxenite gave rise to the observed MORBs and alkali basalts.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Earth, moon and planets 77 (1997), S. 189-198 
    ISSN: 1573-0794
    Schlagwort(e): Comets – Hale–Bopp C/1995 O1 ; rotation ; shape ; morphology
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie , Physik
    Notizen: Abstract We present constraints on the spin state of comet Hale-Bopp based on coma morphology. Three cases of rotational states are compatible with near perihelion observations: (1) principal-axis rotation, (2) complex rotational state with a small precessional angle, or (3) complex rotational state with a large ratio between the component periods. For principal axis rotators, images from 1996 (pre-perihelion) are consistent with a rotational angular momentum vector, M, directed at ecliptic longitude and latitude (250°, -5°) while images from late 1997 (post-perihelion) indicate (310°, -40°). This may suggest a change in M. A complex rotational state with small precessional angle requires only a small or no change in M over the active orbital arc. In this case, M is directed near ecliptic longitude and latitude (270°, -20°). A rotationally excited nucleus with a large ratio between component periods requires the nucleus to be nearly spherical. The transformation of dust coma morphology from near-radial jets to bright arcs and then again to near-radial jets is interpreted as a heliocentric and geocentric distance dependent evolutionary sequence. The spiral structures seen in CN filters near perihelion (in contrast to sunward side arcs seen in continuum) can be explained if the precursor of CN molecules (likely sub-micron grains) are emitted from the nucleus at low levels (≈ 10% of the peak daytime emission) during the nighttime. This may be indicative of a nucleus with a CO-rich active area(s).
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Journal of science education and technology 8 (1999), S. 107-121 
    ISSN: 1573-1839
    Schlagwort(e): Computer simulation ; dissection ; anatomy ; morphology ; science education
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Allgemeine Naturwissenschaft , Technik allgemein
    Notizen: Abstract Science teachers, school administrators, educators, and the scientific community are faced with ethical controversies over animal dissection in classrooms. Simulation has been proposed as a way of dealing with this issue. One intriguing previous finding was that use of an interactive videodisc dissection facilitated performance on a subsequent actual dissection. This study examined the prior use of simulation of frog dissection in improving students' actual dissection performance and learning of frog anatomy and morphology. There were three experimental conditions: simulation before dissection (SBD); dissection before simulation (DBS); or dissection-only (DO). Results of the study indicated that students receiving SBD performed significantly better than students receiving DBS or DO on both actual dissection and knowledge of the anatomy and morphology. Students' attitudes toward the use of animals for dissection did not change significantly from pretest to posttest and did not interact with treatment. The genders did not differ in achievement, but males were more favorable towards dissection and computers than were females.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Earth, moon and planets 75 (1996), S. 53-75 
    ISSN: 1573-0794
    Schlagwort(e): Asteroids ; morphology
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie , Physik
    Notizen: Abstract I present new maps, photomosaics and geological interpretations of asteroid 951 Gaspra. Facets and limb concavities suggest a long history of large impacts producing 5 to 7 km diameter craters. Craters 1 to 4 km in diameter date the last facet-forming impact, though it is not clear which facet this formed. These craters are more numerous than previously thought because much of the area seen at high resolution seems to be depleted in these larger craters. Craters in that area probably date the last body-jolting impact. Linear features, probably the surface expressions of deep fractures, form at least two groups with different trends and probably different ages. Previously noted fresh and spectrally distinct materials are concentrated on ridges. One or two dark markings occur on a steep slope seen at high sun. Smooth materials, probably consisting of thicker or more mobile regolith than elsewhere, occur on steep slopes, usually on rotational leading surfaces.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Earth, moon and planets 78 (1997), S. 197-203 
    ISSN: 1573-0794
    Schlagwort(e): Comets ; Hale-Bopp ; dust ; coma ; morphology ; rotation ; period
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie , Physik
    Notizen: Abstract Dust continuum imaging of comet C/1995 O1 (Hale-Bopp) was carried out with the Swedish Vacuum Solar Telescope (SVST)on La Palma in April, 1997. Images were reduced according to standard procedure, aligned, averaged, navigated and enhanced with azimuthal renormalization, rotational derivative, temporal derivative and unsharp masking processing. The rotational period of the nucleus was determined to 11.5 h and the mean projected dust outflow velocity to 0.41 km s−1. Shell envelopes in the sunward side of the coma were separated by a projected distance of ∼15 000–20 000 km and spiralling inwards towards smaller radii in the direction of local evening. Small scale inhomogeneities of size 1 000–2 000 km, interpreted as correlated with variations in dust emission activity, were seen at radii ≤20 000 km. Two overlapping shell systems with a relative lag angle of ∼55° were evident at the time. The north pole of the nucleus was directed towards the Earth. The dust emission pattern is very complex and may be due to several active areas. The shape of the incomplete spiral shell pattern indicates that the angle between the line-of-sight and the rotational axis of the nucleus was not large.
    Materialart: Digitale Medien
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  • 6
    ISSN: 1573-0794
    Schlagwort(e): C/1995 O1 (Hale-Bopp) ; inner-coma ; morphology ; visible ; infrared
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie , Physik
    Notizen: Abstract We present a comparison between images of comet C/1995 O1 (Hale-Bopp) obtained from 12 March to 9 May 1997, with two telescopes of the Observatorio del Teide (IAC, Tenerife, Spain) in visible (Johnson-V filter) and three near-infrared narrowband filters (Brγ (2.166 μm), CO (2.295 μm), and Kcon (2.260 μm)). No significant differences are observed between the images in the three near-infrared bands suggesting that any CO emission is very weak, or produced by an extended flat source. We do not find evidence for the existence of an additional infrared component due to emission by warm dust, or to dust grains of diverse composition and/or size. Visible and infrared images of the same rotational phase look almost identical, supporting the view that the observed jets and shells are mainly dust structures.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    Rheologica acta 35 (1996), S. 369-381 
    ISSN: 1435-1528
    Schlagwort(e): Melt rheology ; linear and non-linear viscoelasticity ; polymer blends ; reinforced polymers ; morphology ; Cox-Merz rule ; aggregation ; percolation
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Abstract Viscoelastic behavior, phase morphology and flow conditions relationships in polymer/rubber blends have been investigated. The importance of such correlations is illustrated on polymethylmethacrylate (PMMA)/rubber blends subjected to different flow conditions both under small and large deformations. In small-amplitude oscillatory shear (the morphology does not change during the flow) the elastic modulus G′ of the concentrated blends shows a secondary plateau, G′ p , in the low frequency region. This solid-like behavior appears for rubber particle contents beyond the percolation threshold concentration (15%). Morphological observations revealed that for concentrations higher than 15%, the particles are dispersed in a three-dimensional network-type structure. In capillary flow it was found that the network-type structure was destroyed and replaced by an alignment of particles in the flow direction. This morphological modification resulted in a decrease in both viscosity and post-extrusion swell of the blends. Morphological observations revealed that the ordered structure in the flow direction was concentrated only in the skin region of the extrudate, where the shear stress is higher than the secondary plateau, G′ p . A simple kinetic mechanism is proposed to explain the observed morphology. Similarly, steady shear measurements performed in the cone-and-plate geometry revealed alignment of particles in the flow direction for shear stress values higher than G′p.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Springer
    Rheologica acta 36 (1997), S. 406-415 
    ISSN: 1435-1528
    Schlagwort(e): Polymer blends ; shear flow ; morphology ; coalescence ; breakup
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Abstract The steady-state morphology of an immiscible polymer blend in shear flow has been investigated by optical microscopy techniques. The blend is composed by poly-isobutylene (PIB) and poly-dimethylsiloxane (PDMS) of comparable viscosity. Experiments were performed by means of a home-made transparent parallel plate device. The two plates can be independently counterrotated, so that sheared droplets of the dispersed phase can be kept fixed with respect to the microscope point of view, and observed for long times. The distribution of drops and their average size were measured directly during flow at different shear rates and for different blend compositions. It was found that the average drop size in steady-state conditions is a decreasing function of the applied shear rate, and does not depend on blend composition for volume fractions up to 10%. Experiments have proved that, in the shear rate range which could be investigated, the stationary morphology is controlled only by coalescence phenomena, droplet breakup playing no role in determining the size of the dispersed phase. More generally, it has been shown that the steady-state morphology is a function not only of the physical parameters of the blend and of the shear rate, but also of the initial conditions applied to the blend. The steady-state results reported in this paper constitute the first direct experimental confirmation of theoretical models which describe the mechanisms of shear-induced drop coalescence.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Springer
    Rheologica acta 36 (1997), S. 406-415 
    ISSN: 1435-1528
    Schlagwort(e): Key words Polymer blends ; shear flow ; morphology ; coalescence ; breakup
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Abstract The steady-state morphology of an immiscible polymer blend in shear flow has been investigated by optical microscopy techniques. The blend is composed by poly-isobutylene (PIB) and poly-dimethylsiloxane (PDMS) of comparable viscosity. Experiments were performed by means of a home-made transparent parallel plate device. The two plates can be independently counter-rotated, so that sheared droplets of the dispersed phase can be kept fixed with respect to the microscope point of view, and observed for long times. The distribution of drops and their average size were measured directly during flow at different shear rates and for different blend compositions. It was found that the average drop size in steady-state conditions is a decreasing function of the applied shear rate, and does not depend on blend composition for volume fractions up to 10%. Experiments have proved that, in the shear rate range which could be investigated, the stationary morphology is controlled only by coalescence phenomena, droplet breakup playing no role in determining the size of the dispersed phase. More generally, it has been shown that the steady-state morphology is a function not only of the physical parameters of the blend and of the shear rate, but also of the initial conditions applied to the blend. The steady-state results reported in this paper constitute the first direct experimental confirmation of theoretical models which describe the mechanisms of shear-induced drop coalescence.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    Springer
    Journal of statistical physics 90 (1998), S. 1413-1427 
    ISSN: 1572-9613
    Schlagwort(e): Computer simulation ; cellular automata ; nonequilibrium forms of growth ; dendrites ; morphology ; nonequilibrium phase transitions
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract Two-dimensional nonequilibrium growth of crystals (quasistable faceted and dendritic) in the presence of a phase separating impurity is studied by computer simulation. It is shown that there is a gradual modification in this system from quasistable faceted growth to the formation of dendrites when the impurity concentration increases. If there is dendritic growth in the presence of a phase-separating impurity, the cyclic changes in the morphology, expressed through the periodic occurrence of tertiary branches of a dendrite, are observed when the phase-separating impurity concentration is raised. This behavior of the morphology is considered as a reentrant nonequilibrium phase transition.
    Materialart: Digitale Medien
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  • 11
    Digitale Medien
    Digitale Medien
    Springer
    Journal of superconductivity 11 (1998), S. 347-352 
    ISSN: 1572-9605
    Schlagwort(e): Crystal growth ; morphology ; YBCO ; terraced crystals ; step growth
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Elektrotechnik, Elektronik, Nachrichtentechnik , Physik
    Notizen: Abstract The crystal growth and crystal morphology are very important properties of YBa2Cu3O y superconductors. In this work, we approach these problems with polycrystals. Several typical crystal morphologies were observed by scanning electron microscopy, and the terraced crystals with a layer-by-layer structure were found to be the major form for the well-grown YBa2Cu3O y . To interpret the results, a step-growth model was proposed. In this model, each crystal terrace is close-packed with crystal particles in order. And the particles, each consisting of tens of crystal cells, are movable during crystal growth. Particles at edges or margins of small crystals can move to their larger neighboring crystals through diffusion. With this particle diffusion, small crystals vanish and large crystals grow larger. This proposed model is confirmed by experimental observations.
    Materialart: Digitale Medien
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  • 12
    ISSN: 1572-9605
    Schlagwort(e): Nd1Ba2Cu3Oy thin film ; scanning probe microscope ; surface stability ; morphology ; atomic images
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Elektrotechnik, Elektronik, Nachrichtentechnik , Physik
    Notizen: Abstract Recently, superconducting Nd1Ba2Cu3Oy (Ndl23) thin films with high superconducting transition temperature (T c) have been successfully fabricated at our institute employing the standard laser ablation method. In this paper, we report the results of surface characterization of the Nd123 thin films using an ultrahigh vacuum scanning tunneling microscope/spectroscopy (UHV-STM/STS) and an atomic force microscope (AFM) system operated in air. Clear spiral pattern is observed on the surfaces of Nd123 thin films by STM and AFM, suggesting that films are formed by two-dimensional island growth mode. Contour plots of the spirals show that the step heights of the spirals are not always the integer or half-integer number of thec-axis parameter of the structure. This implies that the surface natural termination layer of the films may not be unique. This result is supported byI-V STS measurements. The surface morphology of the Nd123 thin films is compared with that of thec-axis-oriented Y1Ba2Cu3Sy thin films. Surface atomic images of the as-prepared Nd123 thin films are obtained employing both STM and AFM. STS measurements show that most of the surfaces are semiconductive. The results of STS measurements together with the fact that we are able to see the surface atomic images using scanning probe microscopes suggest that exposure to air does not cause serious degradation to the as-prepared surfaces of Nd123 thin films.
    Materialart: Digitale Medien
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  • 13
    Digitale Medien
    Digitale Medien
    Springer
    Interface science 4 (1997), S. 285-302 
    ISSN: 1573-2746
    Schlagwort(e): internal reduction ; metal precipitation ; morphology
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Abstract Metal precipitation occuring during internal reduction of various mixed oxides, such as magnesia or alumina, doped with more noble transition metal oxides, is investigated for different doping contents, reaction temperature and driving forces. The precipitate morphology developing inside the solid oxide matrix and the corresponding orientation relationships between the metal and the oxide phase are analysed by transmission electron microscopy. The evolution of precipitate shape across the reduction scale is interpreted in terms of ageing of the metal inclusions; the various morphologies identified are ascribed to different stages of nucleation, diffusional growth and final equilibration. Precipitate morphology is analysed in terms of diffusion-controlled growth of small metal particles in their local and long range diffusion field. The influence of interfacial energy and related anisotropy is experimentally demonstrated for selected examples. The general role played by these parameters during growth and final equilibration is also discussed. The implications of the elastic strain fields building up during growth of the metal inside the oxide matrix are analysed in view of our experimental results. Shape changes taking place during the growth process are considered to be controlled by local matter transport properties. The influence of the reaction mechanism at an atomic scale and the relative fit of the crystallographic lattices are briefly summarised.
    Materialart: Digitale Medien
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  • 14
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1053-1063 
    ISSN: 0887-6266
    Schlagwort(e): polyethylene ; polypropylene ; supercritical propane ; morphology ; microporosity ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The morphologies of solvent-free, microporous, mechanically self-supporting cylinders of linear polyethylene and isotactic polypropylene, crystallized from solution in supercritical propane, were examined by an SEM technique. The morphology of gels (or foams), obtained with little or no shrinkage from 2% to 35% solutions by weight of polyethylene (99% to 85% porosities), is shown in some detail. Lamellae with very little or considerable mutual organization occur, often in the form of stacks with straight or coiled axes (axialites). Further growth of these can lead to particles with a roughly spherical overall shape and a predominantly radial orientation of the lamellae at the particle surface. Subcooled isotactic polypropylene, on the other hand, crystallizes in the form of perfectly shaped birefringent microspheres of very uniform size. ©1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 20 Ill.
    Materialart: Digitale Medien
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  • 15
    ISSN: 0887-6266
    Schlagwort(e): morphology ; annealing ; UHMWPE gel-film, IR spectral difference ; x-ray diffraction ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: X-ray diffraction of the UHMWPE gel-films has shown that high heating rate annealing of the films causes deformation of the crystallites. The apparent crystal sizes change with the annealing temperature (Ta). With Ta below 110°C, the dimensions of the crystallites in c-axis (Lc) increase associated with the decreasing in a-axis (La) and b-axis (Lb), but the changes are small because of the higher energy barrier. When Ta is raised to 138°C, Lc is nearly doubled its value at 60°C whereas Lb increases and La remains unchanged. IR spectral subtraction was applied to reveal the morphological changes of the gel-films upon annealing. It has been found that bands of the same type of conformation have different sensitivities subject to the thermal treatment at different annealing temperatures. The results can be understood by assuming the changing process being completed through chain segments sliding along the (020) sectors. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 16
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1877-1894 
    ISSN: 0887-6266
    Schlagwort(e): liquid crystals ; crystallization metastable phases ; rates of phase transformation ; morphology ; competition between phases ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The crystallization of the monotropic liquid crystal forming polyether, poly-n-nonyl-4 4′-biphenyl-2-chloroethane, was investigated using DSC calorimetry and polarizing optical microscopy. The principal theme was the nature of crystallization from the nematic liquid crystalline state, which in the monotropic system could be directly compared with the more familiar crystallization from the isotropic melt using one and the same compound. Novel, polarizing optical structures were observed that combine features of both the usual LCPs (fine “grains”) and those of the conventional crystallizeable polymers (spherulites) with differing degrees of prominence of each according to crystallization conditions. The considerations of such structural observations, combined with the calorimetric results and the newly gained information on the kinetics of the crystallization process, reveal an acceleration of the overall crystallization rate at the stage where liquid crystal formation sets in as assessed by calorimetry but not as registered with the polarizing microscope, leading to wider issues regarding the conception of “amorphous crystalline ratio” and its extension to the liquid crystal state. Beyond polymers, the new findings lead to the more general considerations on metastable phases, specifically to their emergence and competition with the phases of ultimate stability. In this respect the present study on a monotropic LCP provides an illustrative example of a more general treatment presented previously. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 17 Ill.
    Materialart: Digitale Medien
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  • 17
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 2281-2287 
    ISSN: 0887-6266
    Schlagwort(e): Ostwald ripening ; polyethylene ; hydrogenated polybutadiene ; blends ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The coarsening in the quiescent melt of the phase-segregated particles of a polymer blend, composed of a narrow molecular weight fraction of an unbranched high-density polyethylene (HDPE) and a highly branched (100 ethyl branches/1000 C atoms) hydrogenated polybutadiene (HPB) was studied. The system was effectively binary, due to the narrow molecular weight and composition distributions of each component. The system was composed of 90 wt % of the HDPE and 10 wt % of the HPB and it formed a two-phase system in the melt at 177°C. The blend was precipitated from xylene solution in order to obtain an initially intimately mixed system. This was the third study in a series of studies of the coarsening of phase-segregated particles in polymer blends. This study was unique in that the system studied was binary in this case while the previous systems were multicomponent. Since the present system was binary, exact thermodynamic calculations of the phase state of this system could be applied with a high level of confidence. The droplet phase particles, which were mainly composed of the HPB, were observed to coarsen on storage in the melt for times of from 5 s to 1 h. At the shortest storage time of 5 s the particles had an average radius of about 0.05 μm and coarsened to about 0.2 μm after 1 h storage in the melt state. Particle dimensions were measured by scanning electron microscopy of n-heptane-etched and gold-coated sections. It was found that the volume of the particles increased linearly with time and that the rate constant of coarsening was Kexp = 1.23 × 10-18 cm3/s and this agreed fairly well with the rate constant calculated from Ostwald ripening theory of Kce = 0.86 × 10-18 cm3/s. In contrast the rate constant for direct particle diffusion and coalescence was Kc = 3.6 × 10-20 cm3/s. Since this was two orders of magnitude smaller than the rate constant for Ostwald ripening, it was concluded that, although the linear increase of volume with time was also consistent with the particle diffusion and coalescence mechanism, this was not a significant contributor to the coarsening mechanism. The major cause for the insignificance of the particle diffusion and coalescence mechanism was the high melt viscosity of the matrix polymers. The application of the Ostwald ripening theory to this system could be made with a high level of confidence because it was binary. It was found that the phase concentration of the droplet phase apparently underwent a rapid increase during the first 1-2 min of storage in the melt, indicating that the system did not reach phase equilibrium (i.e., did not completely phase-segregate) for about 1-2 min. This further indicated that the long-time coarsening regime was not entered until after this length of time. The particle size distributions remained approximately self-similar over the period of coarsening, as predicted by Ostwald ripening theory. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 18
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 2439-2447 
    ISSN: 0887-6266
    Schlagwort(e): morphology ; phase transition ; poly(ether ketone ketone) ; polymorphism ; SAXS ; structure ; time-resolved ; synchrotron x-rays ; WAXD ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Unique crystallization and melting behavior in poly(aryl ether ketone ketone) containing alternated terephthalic and isophthalic moieties were studied by time-resolved synchrotron x-ray methods. Recently, this material has been shown to exhibit three polymorphs (forms I, II, and III). In this work, we further investigated their distinctive thermal properties and found that form I is the dominating and the most thermally stable phase while form II is favored by fast nucleation conditions and is the least stable phase. On the other hand, form III represents a minor intermediate phase that usually coexists with form I and can be transferred from form II and to form I. Structural and morphological changes in form I have been followed by simultaneous wide-angle x-ray diffraction (WAXD)/small-angle x-ray scattering (SAXS) measurements during cold- or melt-crystallization and subsequent melting. In all cases, a larger dimensional change was found in the crystallographic a-axis than the b-axis during heating and cooling. This may be due to the greater lateral stress variation with respect to temperature along the a direction of the primary lamellae which is induced by either the formation of secondary lamellae or the preferential chain-folding direction in poly(aryl ether ketone ketone)s. During the phase transitions of form II ← III in the cold-crystallized specimen and form III ← I in the melt-crystallized samples, lamellar variables (long period, lamellar thickness, and invariant) obtained from SAXS remain almost constant. This indicates that the density distribution in the long spacing is independent of the melting in form II or III. For melt-crystallization, the corresponding changes in unit-cell dimensions and lamellar morphology during the annealing-induced low endotherm are most consistent with the argument that these changes are due to the melting of thin lamellar population. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 11 Ill.
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  • 19
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1843-1854 
    ISSN: 0887-6266
    Schlagwort(e): crystallization ; DNA ; fractionation ; gel-electrophoresis ; morphology ; phase transition ; SALLS ; sonication ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polydisperse DNA of reasonable molecular weights was prepared from a mammalian source via sonication and fractionation. A method for characterizing the molecular weight using gel electrophoresis is described. Quiescent crystallization was studied in thin films of one of the fractions induced by rapidly changing the hydration state isothermally. We report the occurrence of the semicrystalline nature of DNA. The crystal growth occurring via aggregates is best described as sheaves and spherulites from DNA gels in the relative humidity range (RH) corresponding to A-DNA. These habits exhibit primary nucleation and secondary growth, which closely resemble those of melt-crystallized, synthetic macromolecules and, in a follow-up report, will be shown to be lamellar in nature. Small, needle-like crystals are observed for B-DNA hydration levels, and are unstable at lower hydration levels. A transformation from needle to lamellar crystals can occur, even when the primary nucleation of lamellar forms is otherwise absent at that hydration level, through a cylindrical phase exhibiting selective reflection of colored bands. The hydration level plays, in part, the role of the supercooling in this system and the long-known hysteresis in the formation and dissolution of the A-DNA (crystals) can now be viewed in light of those factors known to operate in semicrystalline systems. A morphological phase diagram is developed and is in accord with the known physical evidence. Because this preparation and these morphological observations are without precedence, substantial detail into methodology is included for this first article in the series. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1843-1854, 1997
    Zusätzliches Material: 10 Ill.
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  • 20
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2169-2175 
    ISSN: 0887-6266
    Schlagwort(e): interfacial tension ; block copolymers ; molecular structure ; polymer interface ; morphology ; interfacial adhesion ; pendant drop method ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The effects of the molecular structure of the styrene-isoprene block copolymer on the interfacial tension, the morphology and the interfacial adhesion of polystyrene/polyisoprene were investigated. A reduction in interfacial tension is observed with the addition of a small amount of copolymer, followed by a leveling off as the copolymer concentration exceeds the critical micelle concentration. The reduction in interfacial tension between polystyrene and polyisoprene is more significant when the isoprene-rich diblock copolymer is added than the cases when the symmetric or styrene-rich diblock copolymer is added. The interfacial tension data seem to be consistent with the phase morphology and the interfacial adhesion: the lower the interfacial tension, the smaller the domain size of dispersed phase and the better the interfacial adhesion. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
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  • 21
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2335-2349 
    ISSN: 0887-6266
    Schlagwort(e): morphology ; polysilanes ; thin film ; chain orientation ; spectroscopy ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The effect of confinement on the crystallinity and chain orientation of ultrathin poly(di-n-hexylsilane) films has been investigated using UV absorption, fluorescence and IR spectroscopies. UV absorption measurements in a series of poly(di-n-hexylsilane) films having thicknesses between 50 and 3500 Å have shown that, for thicknesses less than 500 Å, the polymer backbone disorders and extensive crystallization of the films is hindered irrespective of molecular weight or surface hydrophobicity. Fluorescence studies showed that rapid energy transfer occurs from the disordered chain segments to the crystalline ones. The orientation of both the polymer backbone and side chains was probed with IR absorption and grazing incidence reflection measurements. The side chains are extended, although not completely in the all-trans conformation, with their carbon plane mostly perpendicular to the substrate. The backbone lies extended, with the polymer axis parallel to the plane of the film. The hexyl side-chains disorder in films less than 2000 Å thick and this disordering occurs through the introduction of gauche bonds. Our findings suggest the possibility of using thickness to control the chain organization and morphology of a polymer thin film. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 15 Ill.
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  • 22
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1415-1421 
    ISSN: 0887-6266
    Schlagwort(e): epitaxy ; recrystallization ; high-density polyethylene ; isotactic polypropylene ; morphology ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The recrystallization behavior of high-density polyethylene (HDPE) on the highly oriented isotactic polypropylene (iPP) substrates at temperatures below the melting temperature of HDPE has been investigated by means of transmission electron microscopy. The results obtained by the bright-field observation and the electron diffraction show that upon annealing the HDPE-quenched films on the oriented iPP substrates at temperatures below 125°C, only a small amount of HDPE recrystallizes on the iPP substrate with [001]HDPE//[001]iPP, while annealing the HDPE-quenched films at temperatures above 125°C, all of the HDPE crystallites recrystallize epitaxially on the iPP substrate with [001]HDPE//[101]iPP. © 1997 John Wiley & Sons, Inc. J Polym Sci B: 35: 1415-1421, 1997
    Zusätzliches Material: 9 Ill.
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  • 23
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2271-2280 
    ISSN: 0887-6266
    Schlagwort(e): polymer ; blends ; interface ; morphology ; interfacial tension ; breaking thread ; coalescence ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The breaking thread and the sessile drop methods have been used to evaluate the interfacial tension between a polypropylene (PP) and a polyethylene-terephthalate (PET). An excellent correlation was found between the two. The breaking thread technique was then used to evaluate the interfacial tension of these blends at various levels of a styrene-ethylene butylene-styrene grafted with maleic anhydride (SEBS-g-MA) compatibilizer. In order to evaluate the relative roles of coalescence and interfacial tension in controlling dispersed phase size reduction during compatibilization, the morphology of PP/PET 1/99 and 10/90 blends compatibilized by a SEBS-g-MA were studied and compared. The samples were prepared in a Brabender mixer. For the 10/90 blend, the addition of the compatibilizer leads to a typical emulsification curve, and a decrease in dispersed phase size of 3.4 times is observed. For the 1/99 blend, a 1.7 times reduction in particle size is observed. In the latter case, this decrease can only be attributed to the decrease of the interfacial tension. It is evident from these results that the drop in particle size for the 10/90 PP/PET blend after compatibilization is almost equally due to diminished coalescence and interfacial tension reduction. These results were corroborated with the interfacial tension data in the presence of the copolymer. A direct relationship between the drop in dispersed phase size for the 1/99 PP/PET blend and the interfacial tension reduction was found for this predominantly shear mixing device. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2271-2280, 1997
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 24
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2465-2481 
    ISSN: 0887-6266
    Schlagwort(e): tensile drawing ; morphology ; polybutylene ; terephthalate ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The concept of the drawing of a molecular network has been employed to derive a total network draw ratio from the combination of the two deformations occurring in the production of poly(butylene terephthalate), PBT, fibers by the consecutive processes of melt spinning and cold drawing. The mechanical properties of PBT can then be more readily explained in terms of increases in this total network draw ratio. However, the preorientation and crystallization that occurs in the melt-spinning process can occur at different strain rates and temperatures, depending on the wind up speed employed, on the extensional viscosity of the polymer, and on the variation of the extensional viscosity with temperature. Therefore, for polymers such as poly(butylene terephthalate), which can exist in two crystalline forms, the morphology of the final drawn fiber might be expected to depend on the first melt-spinning stage of the process as well as on the total network draw ratio. In this work, density, birefringence, mechanical measurements, and WAXD measurements, which have been made on the melt-spun fibers and on the drawn fibers, are described. Small differences in some of the drawn yarn mechanical properties at the same overall network draw ratio are related to the crystallinity and in particular to differences in the proportion of the α and β phases present in the drawn yarn. These in turn are related to differences in the temperature and stress during melt spinning and drawing. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2465-2481, 1997
    Zusätzliches Material: 18 Ill.
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  • 25
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1751-1767 
    ISSN: 0887-6266
    Schlagwort(e): nylon 6 ; polypropylene ; morphology ; blends ; compatibilization ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Transmission electron microscopy (TEM) was used to examine the morphology of blends of nylon 6 and polypropylene (PP) containing various maleated polypropylenes (PP-g-MA). The size of the dispersed polypropylene particles decreases as the content of maleic anhydride in the PP-g-MA increases for binary blends of nylon 6 and the maleated polypropylenes. Ternary blends of nylon 6, PP, and PP-g-MA show morphologies that depend on the content of maleic anhydride of the PP-g-MA and on the miscibility of PP and PP-g-MA. Blends where PP and PP-g-MA are immiscible show a bimodal distribution of particle sizes. Miscibility of the PP and PP-g-MA was determined by TEM using a special staining technique. Experimental observations of miscibility were further corroborated by thermodynamic calculations. The morphology of the ternary blends was also found to be dependent on the ratio of PP/PP-g-MA. By changing this ratio it was possible to induce drastic changes of morphology, going from a continuous nylon 6 phase to a continuous PP phase at a fixed composition. The mechanical properties of these blends were found to be dependent on their morphology. ©1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 18 Ill.
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  • 26
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1803-1811 
    ISSN: 0887-6266
    Schlagwort(e): ramp rate ; polyimide ; bending-beam technique ; stress ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The stress in films of semirigid and rigid polyimides (PIs) on silicon (Si) substrate has been measured in situ during curing using a newly modified bending beam apparatus. By using the apparatus, the onset of residual stress in the initially solvent-rich films has also been investigated. The stress characteristics of the PI films are strongly ramp rate dependent. Different ramp rates result in markedly different stress patterns, thermo-mechanical properties, and film morphologies. The residual stress at room temperature after curing is scattered around 23-31 MPa for the films of pyromellitic dianhydride-4,4′-oxydianiline (PMDA-ODA). For pyromellitic dianhydride-p-phenylenediamine (PMDA-PDA), it systematically increases from -6 to 28 MPa for ramp rate increasing from 0.5 to 10°C/min. The residual stress is very low in the slowly cured PMDA-PDA films. However, these films have gone through a very high-stress transient state during curing. The maximum transient stress is comparatively higher in the films of PMDA-PDA than in PMDA-ODA. Slowly cured PMDA-PDA films exhibit high structural ordering, high in-plane anisotropy, and low coefficient of thermal expansion. ©1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 27
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1073-1084 
    ISSN: 0887-6266
    Schlagwort(e): (semi-) interpenetrating polymer networks ; morphology ; phase separation (spinodal) ; gelation (thermoreversible) ; polystyrene/methacrylates ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Morphology control in semi-interpenetrating polymer networks has been achieved by means of a two-step process, separating morphology formation and polymerization/crosslinking. Phase textures formed during spinodal liquid/liquid demixing of a solution of atactic polystyrene in methacrylate monomers were arrested by thermoreversible gelation of the polymer-rich phase as this phase passed its glass transition temperature. The phase separated structure was permanently stabilized by low-temperature crosslinking ultraviolet (UV) polymerization of the methacrylate monomer, and studied by transmission electron microscopy. Thus, it was directly observed how the initial demixing process depended on the initial viscosity of the polymer solution and the mode of quenching. Arrest of the earliest stage of spinodal demixing resulted in separated domains of 0.05-0.08 μm thickness, which were separated by a distance of the spinodal wavelength λ. A cocontinuous network only developed in a relatively late stage of demixing. ©1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Ill.
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  • 28
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 47-56 
    ISSN: 0887-6266
    Schlagwort(e): Transcrystallinity ; PTFE fiber/PP composites ; heterogeneous nucleation ; induction time ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Transcrystallization of polypropylene (PP) on the polytetrafluoroethylene (PTFE) fiber was investigated. Both nucleation rate and crystal growth rate were determined by a polarized optical microscope. Based on the theory of heterogeneous nucleation, it has been found that the induction time can correlate well with the nucleation rate in determining the interfacial free energy difference function Δσ. The ratio of Δσ in the bulk matrix to that at the interface is 1.63 which implies the transcrystalline growth is favorable from a thermodynamic point of view. No difference in crystal growth rate of PP has been found in either spherulites or transcrystalline layers. On the basis of regime theory, a transition between regimes II and III was observed at ΔT = 48K. From the morphology studies, it has been found that the thickness of the transcrystalline layer increases with crystallization temperature, from 30 to 120 μm in the temperature range of 110-140°C. The growth of transcrystalline layer is hindered by the spherulites nucleated in the bulk. Moreover, the radius of spherulites adjacent to the transcrystalline layer is much smaller than that distant to the fiber. No significant increase in nucleation density at fiber ends is observed. Effect of internal stresses of fibers on the fiber's nucleating ability is not pronounced. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
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  • 29
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 837-843 
    ISSN: 0887-6266
    Schlagwort(e): polypyrrole ; morphology ; fracture ; permanganic etching ; conducting polymers ; films ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The internal organization within electrochemically polymerized films of the conducting polymers polypyrrole p-toluene sulphonate and polypyrrole sulphate has been examined by scanning electron microscopy (SEM) following transverse fracture and permanganic etching of microtomed cross sections. X-ray scattering studies have shown these two materials to exhibit very different internal ordering: polypyrrole p-toluene sulphonate is thought as being anisotropic, with the counter ions and polypyrrole chains lying down preferentially in the plane of the work electrode, whereas polypyrrole sulphate is considered to be isotropic. Comparison of the internal textures following the two different preparative techniques shows significant differences. Whereas the morphology revealed in transverse fracture surfaces correlates closely with x-ray scattering data, etched surfaces exhibit a morphology that is in good agreement with the direct examination of sections prepared by ultramicrotomy. Despite the apparent contradiction in these two sets of data, a consistent picture of the true morphology (as revealed by permanganic etching) can be deduced and reconciled with the fracture surface micrographs. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 30
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1621-1628 
    ISSN: 0887-6266
    Schlagwort(e): XLPE ; morphology ; aging ; power cable ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The long-term dielectric performance of underground power cable XLPE (cross-linked polyethylene) insulation suffers from poorly understood aging phenomena. A study of the morphological modifications of XLPE due to electrical aging may provide insight for a better understanding of aging mechanisms. The TEM technique has been used to study the XLPE morphology of unaged, laboratory-aged, and field-aged cable samples. A suitable image contrast enhancing and a stabilization of radiation damage were both successfully achieved by staining the sections with ruthenium tetroxide (RuO4), as individual XLPE lamellae were neatly and reproducibly resolved. Image analysis was used to help in the determination of any aging-induced morphological changes. XLPE samples from an unaged cable (D1) has been exposed to a low-energy electron beam, in an attempt to simulate certain conditions thought to occur in electric field-stressed dielectrics. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 31
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1691-1700 
    ISSN: 0887-6266
    Schlagwort(e): polymer ; blend ; interface ; morphology ; diblock copolymer ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Interfacial agents used in the compatibilization of immiscible polymer blends often consist of block copolymers containing at least one segment compatible with each of the two phases of the blend. This work examines the influence of the molecular weight, architecture, and chemical composition of the interfacial agent on its ability to emulsify a polymer blend. The system chosen is a blend containing 80% polystyrene and 20% ethylene-propylene rubber, compatibilized by diblock copolymers of poly(styrene-hydrogenated butadiene). The emulsification curve, which relates the dispersed phase particle size to the concentration of interfacial agent added to the system, was used as a tool to characterize the efficacy of the different interfacial agents. The observed behavior is similar to that of classical emulsions: a rapid drop in phase size at low concentrations of interfacial modifier, followed by a levelling off to an equilibrium diameter value once a “critical” concentration has been reached. For systems compatibilized by symmetrical diblocks (i.e., containing approximately 50% styrene by weight), the volume average particle diameter decreased from 2.7 μm for the unmodified system to about 0.4 μm once interfacial saturation is reached. The critical concentration for emulsification decreased with increasing interfacial agent molecular weight, due to the higher interfacial area occupied by longer molecules; however, this parameter did not affect the equilibrium particle diameter. The asymmetrical diblock copolymer (30% styrene) was found to be less effective than the symmetrical ones over the entire range of concentrations studied (5 to 35% modifier, based on the volume of the minor phase). Asymmetrical diblock copolymers would tend to form micelles, whereas symmetrical copolymers are less constrained at the interface. No significant difference was observed between the emulsifying capability of tapered and pure diblocks of similar composition and molecular weight. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 11 Ill.
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  • 32
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1715-1722 
    ISSN: 0887-6266
    Schlagwort(e): Polymer blends ; spinodal decomposition ; diblock copolymer ; ternary and quaternary models ; scaling ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The dynamics of phase separation in the presence of a diblock copolymer have been studied using ternary and quaternary models of spinodal decomposition. The ternary model treats the block copolymer as a third component that is compatible with each of the mutually incompatible homopolymers. The quaternary model treats the block copolymer as a pair of specially constrained homopolymers. Both models predict core-shell morphologies with the copolymer concentrated at the interface. Both models predict larger domain sizes and less sharp phase boundaries in the early stages of spinodal decomposition. In the late stages, domain sizes are largest for the system of homopolymers without copolymer and smallest when a system containing copolymer is modeled as a quaternary blend. The scaling exponent observed for the quaternary model was s = 0.25 ± 0.02 compared to s ≅ 0.3 for the homopolymers without copolymer and for the ternary model. The quaternary model predicts internal phase separation within a pure diblock copolymer, whenever the corresponding homopolymers are sufficiently incompatible. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 5 Ill.
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  • 33
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2569-2578 
    ISSN: 0887-6266
    Schlagwort(e): polylactide ; membrane formation ; morphology ; crystallization ; liquid-liquid demixing ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The influence of liquid-liquid demixing, solid-liquid demixing, and vitrification on the membrane morphologies obtained from several polylactide-solvent-nonsolvent systems has been investigated. The polymers investigated were the semicrystalline poly-L-lactide (PLLA) and the amorphous poly-DL-lactide (PDLLA). The solvent-nonsolvent systems used were dioxane-water, N-methyl pyrrolidone-water and dioxane-methanol. For each of these systems it was attempted to relate the membrane morphology to the ternary phase diagram at 25°C. It was demonstrated that for the amorphous poly-DL-lactide the intersection of a glass transition and a liquid-liquid miscibility gap in the phase diagram was a prerequisite for the formation of stable membrane structures. For the semicrystalline PLLA a wide variety of morphologies could be obtained ranging from cellular to spherulitical structures. For membrane-forming combinations that show delayed demixing, trends expected on the basis of phase diagrams were in reasonable agreement with the observed membrane morphologies. Only for the rapidly precipitating system PLLA-N-methyl pyrrolidone-water were structures due to liquid-liquid demixing obtained when structures due to solid-liquid demixing were expected. Probably, rapid precipitation conditions promote solid-liquid demixing over liquid-liquid demixing, because the activation energy necessary for liquid-liquid demixing is lower than that for crystallization. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Ill.
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  • 34
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1175-1183 
    ISSN: 0887-6266
    Schlagwort(e): crystallization ; morphology ; chain folding ; lamella ; hydrogen bonding ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Morphologies of solution-grown crystals in systems containing strong and specific intralattice hydrogen bonding (nylons) are compared with systems displaying only van der Waals intracrystal attractions. The latter are shown to produce crystals that clearly mirror the underlying crystallographic symmetry; in the former systems the morphologies are much more complex and disorganized. This difference is discussed in terms of intralattice forces affecting growth rates and chain rearrangement during crystallization. Arguments deriving from differences in lamellar thickening behavior are also used to demonstrate this point. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1175-1183, 1997
    Zusätzliches Material: 3 Ill.
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  • 35
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1889-1899 
    ISSN: 0887-6266
    Schlagwort(e): polymer ; blend ; cocontinuity ; phase inversion ; interface ; morphology ; elasticity ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In this work the level of continuity and cocontinuity for blends of HDPE/PS prepared on a twin-screw extruder have been studied by both morphology and dissolution studies. Addition of SEBS as an interfacial modifier results in a shift of the percolation threshold for dispersed PS to higher concentrations. The region of phase inversion, however, is maintained at 70% PS. The shift in the percolation threshold to higher values is related to reduced elongation of the PS dispersed phase after interfacial compatibilization. These results indicate that an interfacial modifier significantly influences percolation phenomena without shifting the region of phase inversion. Models based on viscosity ratio have failed to predict the region of phase inversion in this study. Elastic effects are shown to be able to describe the basic tendencies. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1889-1899, 1998
    Zusätzliches Material: 7 Ill.
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  • 36
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1769-1780 
    ISSN: 0887-6266
    Schlagwort(e): polymer blends ; liquid crystalline polymer ; microfibers ; viscosity reduction ; rheology ; morphology ; X-ray scattering ; composite materials ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Immiscible blends of thermotropic liquid crystalline polymers (TLCP) and a flexible polymer matrix show viscosity reductions and extensive fiber formation under certain flow conditions. Here we study these phenomena by directly examining the TLCP component's molecular orientation and the dispersed phase morphology. The rheology and morphology of blends of polybutylene terephthalate and a thermotropic copolyester (HX-8000 series, DuPont) at concentrations varying from 5 to 30 wt % of TLCP are characterized. It is found that the blends show viscosity reduction as well as stable fiber formation at shear rates dependent on the TLCP content. Wide-angle X-ray scattering is performed to measure the degree of molecular orientation of the TLCP phase. A deconvolution scheme isolates the scattering from the TLCP in the blends and a molecular model enables extracting an experimental orientation factor. It was found that a highly microfibrillated TLCP phase is coupled with an increase in the TLCP molecular orientation to values close to the pure TLCP at similar processing conditions. Further, the microfibrillated TLCP phase is found to be stable within the testing time. Current hypotheses about fiber formation in immiscible blends are tested against the experimental observations. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1769-1780, 1998
    Zusätzliches Material: 10 Ill.
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  • 37
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2057-2067 
    ISSN: 0887-6266
    Schlagwort(e): PTFE ; fillers ; UV radiation ; degradation ; morphology ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The first part of a series of two, this paper analyzes the degradation of pure and filled PTFE under high energy UV radiation. The polymer morphology is first investigated using differential scanning calorimetry, highlighting the respective nucleating efficiency of TiO2 and CaF2 during polymer crystallization. Then, the various polymers are exposed to excimer laser radiation and observed under an optical microscope. The results indicate that the degradation is closely connected with microstructural parameters. In pure PTFE, scattering by crystallites and reflection on piles of lamellae control the nature and extent of the degradation. In filled PTFE, nature and concentration of fillers are the most important features governing degradation. When absorbing particles are added to PTFE, the damage is restricted to the surface and photothermal processes can modify the degradation from heterogeneous to ablative, depending on the filler content. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2057-2067, 1998
    Zusätzliches Material: 12 Ill.
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  • 38
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1443-1450 
    ISSN: 0887-6266
    Schlagwort(e): poly(ethylene terephthalate) ; STEM ; dark field imaging ; chemical derivatization ; morphology ; semicrystalline ; amorphous ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Important chemical and mechanical properties in semicrystalline polymers are determined by the noncrystalline or nonordered regions. Hence, characterizing these regions is important in developing a morphological model to better define and predict the chemical and mechanical behavior of polymeric materials. With this objective, preferential tagging was accomplished by covalent linking of a heavy element to poly(ethylene terephthalate) (PET). In scanning transmission electron microscopy (STEM), contrast was obtained using a low concentration of thallium (0.4%), the tagging element, thus providing a map of the more accessible regions within the semicrystalline structure. Differential scanning calorimetry (DSC) and wide-angle x-ray scattering (WAXS) were used to characterize the PET film. Elemental analysis using energy dispersive x-ray analysis (EDAX) was used to confirm the presence of the heavy element in the tagged regions. The STEM imaging results were then compared with the characterization results from the DSC and WAXS measurements to gain an understanding of the domains and their size ranges in the semicrystalline microstructure of PET. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1443-1450, 1998
    Zusätzliches Material: 5 Ill.
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  • 39
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2849-2863 
    ISSN: 0887-6266
    Schlagwort(e): nylon oligoamides ; new crystal structure ; morphology ; crystallization ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Three-amide oligomers of nylon 6 and nylon 6 6 have been investigated using electron microscopy (imaging and diffraction), X-ray diffraction, and computational modeling. A new crystal structure has been discovered for the three-amide oligomer of nylon 6. This material crystallizes from chloroform/dodecane solutions into an unfolded crystal form that has progressively sheared hydrogen bonding in two directions between polar (unidirectional) chains. This structure is quite different from the usual room temperature α-phase structure of chain-folded nylon 6 crystals, in which alternatingly sheared hydrogen bonding occurs between chains of opposite polarity in only one direction. The occurrence of this new structure illustrates the extent to which progressively sheared hydrogen bonding is preferred over alternatingly sheared hydrogen bonding. Indeed, the progressive hydrogen bonding scheme occurs in the three-amide nylon 6 material even though it requires a disruption to the lowest potential energy all-trans conformation of the chain backbone, and requires all the chains in each hydrogen-bonded layer to be aligned in the same direction. We believe the presence of chain folding, which necessarily incorporates adjacent chains of opposite polarity into the crystal structure, prevents the formation of this new crystal structure in the nylon 6 polymer. In contrast, the three-amide nylon 6 6 crystal structure is analogous to the polymeric nylon 6 6 α-phase structure, found in both fibers and chain-folded crystals, and consists of progressive hydrogen-bonded sheets which stack with a progressive shear. In both structures, the molecules (≈ 3 nm in length) form smectic C-like layers with well-orchestrated stacking of 2.2 nm to form a three-dimensional crystal. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2849-2863, 1998
    Zusätzliches Material: 10 Ill.
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  • 40
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2267-2274 
    ISSN: 0887-6266
    Schlagwort(e): poly(ether ether kotone) ; polyimide ; miscibility ; crystallization ; morphology ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Miscibility and crystallization behavior of solution-blended poly(ether ether ketone)/polyimide (PEEK/PI) blends were investigated by using DSC, optical microscopy and SAXS methods. Two kinds of PIs, YS-30 and PEI-E, which consist of the same diamine but different dianhydrides, were used in this work. The experimental results show that blends of PEEK/YS-30 are miscible over the entire composition range, as all the blends of different compositions exhibit a single glass transition temperature. The crystallization of PEEK was hindered by YS-30 in PEEK/YS-30 blends, of which the dominant morphology is interlamellar. On the other hand, blends of PEEK/PEI-E are immiscible, and the effect of PEI-E on the crystallization behavior of PEEK is weak. The crystallinity of PEEK in the isothermally crystallized PEEK/YS-30 blend specimens decreases with the increase in PI content. But the crystallinity of PEEK in the annealed samples almost keeps unchanged and reaches its maximum value, which is more than 50%. The spherulitic texture of the blends depends on both the blend composition and the molecular structure of the PIs used. The more PI added, the more imperfect the crystalline structure of PEEK. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2267-2274, 1998
    Zusätzliches Material: 9 Ill.
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  • 41
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2961-2970 
    ISSN: 0887-6266
    Schlagwort(e): micelle ; blends ; crystallization ; morphology ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The crystallization, morphology, and crystalline structure of dilute solid solutions of tetrahydrofuran-methyl methacrylate diblock copolymer (PTHF-b-PMMA) in poly(ethylene oxide) (PEO) and PTHF have been studied with differential scanning calorimetry (DSC), X-ray, and optical microscopy. This study provides a new insight into the crystallization behavior of block copolymers. For the dilute PTHF-b-PMMA/PEO system containing only 2 to 7 wt % of PTHF content, crystallization of the PTHF micellar core was detected both on cooling and on heating. Compared the crystallization of the PTHF in the dilute solutions with that in the pure copolymer, it was found that the crystallizability of the PTHF micellar core in the solution is much greater than that of the dispersed PTHF microdomain in the pure copolymer. The stronger crystallizability in the solution was presumably due to a softened PMMA corona formed in the solution of the copolymer with PEO. However, the “soft” micelles formed in the solution (meaning that the glass transition temperatures (Tg) of the micelle is lower than the Tm of the matrix phase) showed almost no effects on the spherulitic morphology of the PEO component, compared with that of the pure PEO sample. In contrast, significant effects of the micelles with a “hard” PMMA core (meaning that the Tg of the core is higher than the Tm of the PTHF homopolymer) on the nucleation, crystalline structure, and spherulitic morphology were observed for the dilute PTHF-b-PMMA/PTHF system. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2961-2970, 1998
    Zusätzliches Material: 9 Ill.
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  • 42
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 637-655 
    ISSN: 0887-6266
    Schlagwort(e): organic-inorganic composites ; sol-gel ; TEOS ; TMOS ; SAXS ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Two morphological models have been proposed to describe small-angle x-ray scattering from organic-inorganic composite (OIC) materials. The first model invokes the idea of a liquid-like arrangement among noninterpenetrating fractal clusters, and the second employs an empirical correlation function that would be expected for a bicontinuous two-phase (B2P) picture with the inorganic portion exhibiting fractal characteristics. Simulated scattering profiles have been generated for direct comparison with experimental data. The samples studied were a triethoxysilane-endcapped bisphenol A epoxide resin (EAS) reacted in the presence of tetraethoxysilane (TEOS) under slightly basic conditions, and a random trimethoxysilane-functionalized copolymer of poly(methyl methacrylate) (MMA-TMS) with added tetramethoxysilane (TMOS), reacted in an acidic medium. Each morphology model qualitatively simulates the broad scattering maximum and limiting high-angle slope commonly seen in SAXS profiles. It is concluded that the inorganic phase in the EAS hybrid exhibits particle-like characteristics at length scales less than approximately 250 Å, and the organic and inorganic components are bicontinuous at larger distances. The MMATMS composite is better described by bicontinuous organic and inorganic phases with a periodic fluctuation of about 40 Å. The scattering maximum arises either from the mean separation of particles or a dominant wavelength in a concentration fluctuation, similar to that observed for spinodal decomposition. In either case, the SAXS peak position is related to the distance between junction points of the crosslinked organic polymer. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 16 Ill.
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  • 43
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 225-232 
    ISSN: 0887-6266
    Schlagwort(e): polyurethane ionomer ; transesterification ; morphology ; phase compatibility ; ionic cluster ; solid-state ionic conductivity ; single ion transport mechanism ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A series of polyether (PTMO, PEO) polyurethane ionomers having different contents of sodium sulfonate groups in the soft segments have been synthesized. The reaction of transesterification was involved in the incorporation of the sodium sulfonate groups in the polyether. The polyurethane ionomers were characterized by means of dynamic mechanical thermal analysis, differential scanning calorimetry, and small-angle x-ray scattering. Solid-state ionic conductivity was also measured. As the ionization level increased, the compatibility of the hard and soft segments increased and the glass transition region of the soft segment became broader. These samples had relatively higher moduli and good film-forming ability. Moreover, this kind of ionomer provides a very promising ionic conductive multiphase polymer with a single ion transport mechanism. © 1997 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Ill.
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  • 44
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2689-2713 
    ISSN: 0887-6266
    Schlagwort(e): homogeneous copolymers ; thermal behavior ; morphology ; DSC ; SAXS ; WAXD ; SALLS ; OM ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The morphology of homogeneous copolymers of ethene and 1-octene synthesized using a V-based Ziegler-Natta catalyst was studied as a function of the short chain branching content (SCBC) and the molar mass. Linear polyethylenes (LPE) were used as reference material. For the linear samples an increase in molar mass results in an increase of the long period and the crystalline lamella thickness. A decrease of cooling rate results in an increase of the melting temperature, the long period and the crystalline lamella thickness and an evolution from spherulitic structures to perfectly stacked lamellae. For the branched samples, increasing the SCBC results in a decrease of the melting and the crystallization temperature, crystallinity, spherulite radius, the long period, and the crystalline lamella thickness. The two latter tend to a limiting value on reaching a SCBC of 20CH3/1000C. On the other hand, an increase of the a axis and to a lesser extent the b axis of the unit cell is observed. Decreasing the cooling rate affects only the crystallinity of the least branched samples. Furthermore decreasing the cooling rate results in smaller spherulites, has a minor influence on the lamellar parameters and reduces the dimensions of the basal plane of the unit cell. Increasing the molar mass of the branched samples results in a drop of the crystallinity, a deterioration of the superstructure, enlarges the amorphous layer thickness and the dimensions of the basal plane. All these observations can be accounted for by the different crystallization regimes being applicable when different molar masses, SCBC and cooling rates are used. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2689-2713, 1997
    Zusätzliches Material: 15 Ill.
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  • 45
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2457-2464 
    ISSN: 0887-6266
    Schlagwort(e): polyamide 6 ; aluminum borate whiskers ; poly(ε-caprolactam) ; crystallinity ; composites ; interphase ; morphology ; wide-angle X-ray scattering ; differential scanning calorimetry ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The influence of aluminum borate whiskers upon the morphology of polyamide 6 was studied by wide-angle X-ray scattering and by differential scanning calorimetry. The whiskers did not promote the formation of either the hexagonal γ or the monoclinic β crystalline phase. A new experimental procedure has been devised for the production of very thin polymer layers on the whiskers. In the procedure, styrene co-acrylonitrile polymer is used as a processing aid and is later extracted. The procedure allows for the generation of polyamide layers less than 30 nm thick. Crystallinity in these thin layers was suppressed. An expression has been developed to characterize the crystallinity gradient in the interphase of the whisker surface. The equation shows that the initial 1.4 nm of polymer is fully amorphous and produces excellent evaluations of the crystallinity gradient to layer thicknesses of 70 nm. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2457-2464, 1997
    Zusätzliches Material: 7 Ill.
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  • 46
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2523-2533 
    ISSN: 0887-6266
    Schlagwort(e): chirality ; morphology ; structure ; crystallization ; defects ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In previous work we have shown that the stable form of syndiotactic polypropylene (sPP) adopts a fully antichiral packing in its crystalline lattice. At the same time, we had also discovered a number of prohibited reflections from crystallographic planes with a c-axis component, indicating distortions or defects along the molecular-chain direction and possible departures from the ideal Ibca unit-cell structure. Three studies that appeared in 1996 have proposed a number of possible minimized structures to explore the energetics of departure from such an ideal Ibca symmetry and to account for the prohibited reflections. Two of the studies were based upon energy minimization of the unit cell using empirical or spectroscopically derived force fields. The third model was based upon Rietveld refinement of the bulk X-ray diffractogram combined with ad hoc choices of space groups selected to reproduce the prohibited reflections, and results in a structure with minimal departures from Ibca. In the present article we examine the structural implications of all these models on various reciprocal-lattice sections of sPP by comparing calculated electron-diffraction patterns for appropriate zones with those we obtained experimentally from single crystals. We find that none of the proposed models fully accounts for the experimental data. One of the energy-minimized models (involving translation along the molecular axis) and the Rietveld-refined structure reproduce some of the observed reflections but are not in agreement with observed intensities and introduce additional unobserved reflections or other artifacts. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2523-2533, 1997
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
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  • 47
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1807-1820 
    ISSN: 0887-6266
    Schlagwort(e): poly(p-oxybenzoate) ; confined thin film melt polymerization ; epitaxy ; mica substrate ; morphology ; crystal structure ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polymerization of p-acetoxybenzoic acid between mica sheets, from both the melt and dilute solution, in a wide range of polymerization temperatures (180-400°C) yields an epitaxial-like overgrowth of PpOBA on the mica cleavage surface. The PpOBA overgrowth forms long rows by lateral aggregation of ribbon crystals situated in three substrate directions rotated by 60°. The c-axes of the PpOBA phase I and II lattices are parallel to the 001 plane of the mica, coinciding with the a-axes of the mica hexagonal structure. The aI- and bII-axes lie predominantly on the mica surface. The surface-orienting effect is tentatively attributed to surface steps and or/polar effects; lattice matching does not occur. The recrystallization of bulk polymer samples previously prepared also leads to ordering between mica like that in melt or solution polymerization. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1807-1820, 1997
    Zusätzliches Material: 12 Ill.
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  • 48
    ISSN: 0887-6266
    Schlagwort(e): poly(methylphenylsiloxane) ; poly(dimethylsiloxane) ; titania ; silica ; composites ; reinforced elastomers ; morphology ; stress-strain isotherms ; scattering intensities ; differential scanning calorimetry ; transmission electron microscopy ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The work reported in the preceding article in this series is extended by consideration of polysiloxane-ceramic composites based on atactic poly(methylphenylsiloxane) (PMPS) elastomers instead of poly(dimethylsiloxane). The former is noncrystallizable because of its stereochemically irregular structure, while the latter is crystallizable. In addition, some composites were prepared by the in situ precipitation of titania instead of silica. The resulting materials were characterized using differential scanning calorimetry, equilibrium stress-strain measurements in elongation, small-angle neutron scattering, and transmission electron microscopy. The moduli of the PMPS elastomers were found to increase significantly with increase in amount of either type of filler, with reinforcing upturns at high elongation in the case of the silica. Because the PMPS elastomers were amorphous, it is obvious that strain-induced crystallization is not required for these upturns in modulus. Titania did not give as good reinforcement as did silica, at least in the case of PMPS. Differences in interactions between the polymer and the two fillers are obviously important in this regard, but differences in particle morphology probably also contribute. Specifically, the titania “particles” were significantly larger than the silica particles when observed in TEM, and appeared to be much more porous. The actual domain size as measured by scattering, however, was only approximately 5% larger. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1191-1200, 1998
    Zusätzliches Material: 9 Ill.
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  • 49
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 247-252 
    ISSN: 0887-6266
    Schlagwort(e): block copolymers ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Contrast for transmission electron microscopy (TEM) of microphase-separated saturated hydrocarbon diblock copolymers has been obtained using ruthenium tetroxide (RuO4). This technique exploits differences in the rate of transport of the oxidizing stain in rubbery amorphous versus semicrystalline, or glassy, microdomains. Rapid quenching from above the melting (Tm), or glass transition (Tg) temperature is shown to preserve the equilibrium melt morphology in poly(ethylene)-poly(ethyl-ethylene) (PE-PEE), poly(ethylene)-poly(ethylene-propylene) (PE-PEP), and poly(vinylcyclohexane)-poly(ethyl-ethylene) (PVCH-PEE) diblock copolymers; PE melts at 108°C, PVCH is glassy up to about 140°C, while PEE and PEP remain rubbery down to approximately-20°C and -56°C, respectively. Treatment of ultrathin sections of the quenched specimens with RuO4 vapor led to welldefined TEM images, that revealed microdomain type and order. These results are consistent with SANS data taken under equilibrium conditions. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 5 Ill.
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  • 50
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1313-1322 
    ISSN: 0887-6266
    Schlagwort(e): mechanical properties ; morphology ; fracture ; J-integral ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: An adaptation of the fracture toughness test method, the J-integral technique, is described within the general framework of polymer fracture behavior. It is shown that there is a strong interaction between different morphological parameters in the way they affect the fracture behavior of isotactic polypropylene (iPP). The fracture toughness decreases with increasing crystallinity at a fixed spherulite size. The fracture toughness also decreases slightly with increasing spherulite size at a constant crystallinity, but this may not be a pure spherulite size effect. The use of a nucleating agent results in a very fine spherulitic structure but facilitates crack growth and reduces the material toughness beyond the crack initiation stage. This suggests that the material behavior is dictated by the increase in crystallization temperature caused by the presence of the nucleating agent and not by the change in spherulite size. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 13 Ill.
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  • 51
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 707-715 
    ISSN: 0887-6266
    Schlagwort(e): PEEK ; morphology ; transparency ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: We report a processing window in which transparent semicrystalline poly(ether ether ketone) (PEEK) can be produced. The transparent PEEK film reported is 100 μm in thickness and has light transmittance of 54%; while ordinary semicrystalline PEEK film of the same thickness and degree of crystallinity, but produced outside the processing window, is virtually opaque (with the light transmittance close to 0%). First processing conditions for producing the transparent PEEK film are discussed, and second characterization of the transparent PEEK film is detailed. Results suggest that the main processing condition for developing the transparent PEEK film is forming temperature, defined as the highest temperature that the film is exposed to during thermal treatment. Using transmission electron microscopy (TEM), differential scanning calorimetry (DSC), and small-angle x-ray scattering (SAXS), we characterized morphology of the PEEK films. TEM shows that the morphology in the transparent PEEK film has a locally oriented lamellar structure, instead of the commonly observed spherulites or sheaves. DSC results suggest that the new morphology is formed in the melt with a high density of residual crystals that act as nucleating agents during the crystallization process, which is known as a self-seeding effect. SAXS spectra show that specimens with higher forming temperature produce broader diffraction peak at larger Q value that is defined as 4π sin θ/λ. We conclude from the study that the light transmittance enhancement is morphology related, and can be achieved through control of processing conditions. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 9 Ill.
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  • 52
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2843-2851 
    ISSN: 0887-6266
    Schlagwort(e): poly(terephthalic anhydride) ; crystal structure ; single crystals ; morphology ; confined thin film melt polymerization ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Single crystals of poly(terephthalic anhydride) (PTA) have been grown using the confined thin film melt polymerization technique. Thin lamellae (ca. 50 Å) are found for low polymerization temperatures, with thick crystals forming for polymerization at 200°C. Shearing of the material shortly after the initiation of polymerization at 200°C yielded single crystal domains composed of fibrillar texture material; these samples gave [010] zone ED patterns complementing the [001] zone patterns from the unsheared CTFMP samples. A monoclinic, single chain, two repeat unit, unit cell (Pc11) is proposed based on four different electron diffraction zone patterns: a = 6.01 Å, b = 3.945 Å, c = 14.11 Å, α = 106.9°. Simulations, using the Cerius2 program, of the corresponding molecular conformation, packing and electron diffraction (ED) patterns were performed; the ED simulations are in good agreement with the observed patterns. An R-factor of 0.23 is obtained based on a comparison of calculated and observed structure factors for the 39 independent ED reflections observed on the different zone patterns. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 9 Ill.
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  • 53
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 173-185 
    ISSN: 0887-6266
    Schlagwort(e): coagulation ; low dielectric constant ; fiber ; miscibility ; morphology ; solution spinning ; polyimide ; precipitation strength ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Control of the internal morphology of wet-spun fibers from a fluorinated polyimide has been achieved by varying the rate of polymer coagulation through adjustments in nonsolvent/solvent miscibility and precipitation strength of the coagulation bath. Filament internal morphologies ranged from very porous or sponge-like to fully solid. Intermediate structures included fibers containing a spongy core with a nonporous skin, sponge-like fibers containing large voids, and a relatively solid material containing randomly spaced small voids. The cross-sectional shape of the fiber is dependent upon the coagulation process as well as the volume contraction of the initial extrudate. Drawn fibers (3×) retained the original asspun cross-sectional shape and also lost porosity. Mechanical properties of poly(6FDA-4BDAF) fibers have an inverse relationship to filament porosity. Maximum modulus and break strength for drawn fibers is approximately 6 CPa and 200 MPa, respectively. Asspun mechanical properties were dependent upon the processing conditions and have moduli between 0.4-3.0 Gpa and break strengths of 10-160 MPa. A dielectric constant of 2.50 for nonporous films was measured over a frequency range between 1.0 MHz to 1.8 GHz, showing little dispersion. © 1997 John Wiley & Sons, Inc.
    Zusätzliches Material: 6 Ill.
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  • 54
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 293-308 
    ISSN: 0887-6266
    Schlagwort(e): polymer blends ; morphology ; stability ; co-continuity ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The morphological stability of polystyrene high-density polyethylene (PS/PE) blend is investigated in the region of dual-phase continuity. The effect of the addition of a triblock SEBS copolymer to the blends on the stability of these morphologies, is examined. The results show that the morphology of the unmodified blends changes from co-continuous to droplet matrix for PS-rich blends whereas the morphology of a 50/50 blend maintains continuity but coarsened significantly upon annealing at 200°C. In the presence of the copolymer, these morphologies are much more stable. Selective solvent extraction of polystyrene in di-ethyl ether reveals that the level of PS continuity in the 50/50 blend is higher for the unmodified system than for the modified one. Upon annealing, the level of PS continuity significantly increases for the unmodified 50/50 PS/PE blend. The effect of the copolymer content in the blend on the interfacial tension between the two components is also investigated using the breaking thread method. The interfacial tension is found to be reduced from 5.6 to 1.1 mN/m by the addition of 20 parts of the copolymer to the blend. © 1997 John Wiley & Sons, Inc.
    Zusätzliches Material: 14 Ill.
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  • 55
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 415-430 
    ISSN: 0887-6266
    Schlagwort(e): aliphatic polyketone ; ethylene-carbon monoxide copolymer ; PK ; isotactic polypropylene ; injection moulding ; molecular alignment ; morphology ; SCORIM ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: This article relates to an investigation of injection moulding a new commercial polymer, an aliphatic polyketone (PK). A terpolymer and a 30% glass-filled grade were used as study materials together with an isotactic polypropylene that was used as a basis for comparison. Both conventional injection moulding and shear-controlled orientation injection moulding (SCORIM) were employed in processing. Tensile testing was carried out at 80°C as well as at room temperature. Polarized light microscopy and wide-angle x-ray diffraction were used in the characterization of the mouldings. An increase of up to 30% in Young's modulus and 35% in ultimate tensile strength, and a 70-90% increase in strain at peak were gained for the terpolymer (PK) at room temperature, as a result of SCORIM processing. A substantial improvement at 80°C was also recorded for unfilled SCORIM PK mouldings, and is attributed to the pronounced molecular alignment that was induced in SCORIM mouldings, as shown by Debye patterns. It is notable that the SCORIM mouldings of PK exhibit a greater tensile strength at 80°C than the SCORIM mouldings of isotactic polypropylene at 23°C. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys, 35: 415-430, 1997
    Zusätzliches Material: 17 Ill.
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  • 56
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 953-961 
    ISSN: 0887-6266
    Schlagwort(e): ethylene-1-hexene copolymer ; polypropylene ; polymer blend ; miscibility ; crystallization ; morphology ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Morphology and isothermal growth rates of spherulites for the binary blends consisting of an isotactic polypropylene (i-PP) and an ethylene-1-hexene rubber (EHR) were examined as a function of the crystallization temperature ranging from 388 K to 418 K. In this study, two types of EHR's were employed: “ethylene rich” EHR and “1-hexene rich” EHR. The blends of i-PP with the EHR of 51 mol % 1-hexene are miscible in the molten state, whereas the blends with the EHR of 33 mol % 1-hexene are immiscible in the molten state. It is found that the isothermal spherulite growth rate of the miscible i-PP/EHR blends decreases with increasing the EHR fraction, whereas the spherulite growth rate of the immiscible i-PP/EHR blends is independent of the blend composition and is the same as that of the i-PP. Optical microscope observation of the miscible blends crystallized isothermally shows that there are no rubber domains either in the intraspherulitic or in the interspherulitic contact regions. On the other hand, the immiscible i-PP/EHR blends show a phase-separated morphology. Furthermore, the number of tangential lamellae of the miscible i-PP/EHR blends is found to be increased by blending of the EHR, leading to the spherulite with negative birefringence. The sign of birefringence of spherulites is unaffected by the regime transition as well as by the fold surface free energy. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 953-961, 1997
    Zusätzliches Material: 7 Ill.
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  • 57
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1757-1774 
    ISSN: 0887-6266
    Schlagwort(e): polyesters ; crystallization ; melting ; morphology ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The melting behavior of isothermally crystallized PET has been studied using linear heating in a differential scanning calorimeter (DSC). Variables such as crystallization temperature, crystallization time, heating rate, and average molecular weight are the main focus of the study. On the basis of several experimental techniques, a correlation of the melting behavior of PET with the amount of secondary crystallization was found to exist. It was observed that the triple melting of PET is a function of programmable DSC variables such as crystallization temperature, crystallization time, and heating rate. However, in testing the hypothesis that there was a correlation between melting endotherms and secondary crystallization inside spherulites, it was found necessary to use a DSC-independent variable in order to enhance the observed effects. Therefore, on the basis of a crystallization model that involves secondary branching along the edges of parent lamellar structures, it was speculated that an increase in the average molecular weight could affect the triple melting of PET due to an increase of rejected portions of the macromolecules. It was found that the second melting endotherm increased, apparently, at the expense of the third one as the average molecular weight was increased. The second melting endotherm was also found to correlate proportionally with the amount of secondary crystallization inside spherulites. The results support a model of crystallization which basically consists of parent crystals and at least one population of secondary, probably metastable, crystals. This latter structural component must involve excluded portions of the macromolecules that did not crystallize during the isothermal crystallization period of the parent crystals. An increase of molecular weight gives rise to a higher entanglement density which in turn increases the fraction of initially rejected chain sections and therefore the amount of secondary crystallization. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1757-1774, 1997
    Zusätzliches Material: 17 Ill.
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  • 58
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2583-2592 
    ISSN: 0887-6266
    Schlagwort(e): nylon-6 ; ABS ; blends ; morphology ; fracture ; mechanics ; impact ; mechanical properties ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Tensile and impact properties of uncompatibilized nylon-6/ABS blends have been studied over the entire range of compositions. The blends were prepared by extrusion and, subsequently, injection molded into tensile specimens and rectangular plaques. The impact fracture performance was characterized using recently proposed models based on fracture mechanics, for various fracture behaviors. The results showed that nylon-6 breaks in a brittle manner. With the addition of ABS, the blend exhibits the same behavior with a slightly lower impact resistance up to about 60 wt %. A sudden jump in the value of impact fracture energy is observed around 70 wt % ABS with a brittle - ductile transition in the mechanism of fracture. The transition in fracture mechanisms is confirmed through observation of the fracture surfaces by scanning electron microscopy (SEM). Tensile tests showed that the elongation at break increases only slightly between 0 and 50% ABS content, but a significant jump occurs around 70% ABS, reaching a 6-fold increase in comparison to that of the pure components. SEM observation of etched samples shows that a cocontinuous morphology occurs around 70 wt % ABS. The peak observed for the elongation at break and the jump in impact performance, as well as the onset of brittle-ductile transition, are attributed to this morphological effect. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2583-2592, 1997
    Zusätzliches Material: 13 Ill.
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  • 59
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2825-2833 
    ISSN: 0887-6266
    Schlagwort(e): holographic gratings ; morphology ; functionality ; liquid-gel demixing ; network ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The morphology of transmission gratings with varying Bragg spacings formed using polymer-dispersed liquid crystals were examined using high-resolution scanning electron microscopy and image analysis techniques. The effect on the morphology of small changes in the overall functionality of the prepolymer syrup was observed. An increase in the amount of monofunctional compound resulted in small, nearly spherical domains (〈100 nm in diameter) confined in well-defined lamellae for samples with a 0.49 μm Bragg spacing. A decrease in concentration (an effective increase in monomer functionality) at this Bragg spacing resulted in larger domains (100-200 nm) with much greater distribution of sizes and shapes. The local volume fractions of discrete liquid crystalline (LC) domains was considerably larger in the latter case. An increase in the Bragg spacing to 1.35 μm also resulted in well-defined lamellae of LC domains, although much more coalescence into irregularly shaped individual domains was observed. Surprisingly, the local volume fraction of LC increased in the larger Bragg spacing samples. The morphology results are discussed qualitatively in terms of liquid-gel demixing where the inherent crosslink density and elasticity of the polymeric host must be considered in phase separation processes on the nanoscale. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2825-2833, 1997
    Zusätzliches Material: 6 Ill.
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  • 60
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2551-2562 
    ISSN: 0887-6266
    Schlagwort(e): polytetrafluoroethylene ; virgin powder ; two-stage draw ; morphology ; tensile properties ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polytetrafluoroethylene (PTFE) virgin powder was ultradrawn uniaxially by a two-stage draw. A film, compression molded from powder below the melting temperature (Tm), was initially solid-state coextruded to an extrudate draw ratio (EDR) of 6-20 at an established optimum extrusion temperature of 325°C, near the Tm of 335°C. These extrudates from first draw were found to exhibit the highest ductility at 45-100°C for the second-stage tensile draw, depending on the initial EDR and draw rate. The maximum achievable total draw ratio (DRt, max) was 36-48. Such high ductility of PTFE, far below the Tg (125°C) and Tm, is in sharp contrast to other crystalline polymers that generally exhibit the highest ductility above their Tg and near Tm. The unusual draw characteristics of PTFE was ascribed to the existence of the reversible crystal/crystal transitions around room temperature and the low intermolecular force of this polymer, which leads to a rapid decrease in tensile strength with temperature. The structure and tensile properties of drawn products were sensitive to the initial EDR, although this had no significant influence on DRt,max. The most efficient and highest draw was achieved by the second-stage tensile draw of an extrudate with the highest EDR 20 at 100°C, as evaluated by the morphological and tensile properties as a function of DRt. The efficiency of draw for the cold tensile draw at 100°C was a little lower than that for solid-state coextrusion near the Tm. However, significantly higher tensile modulus and strength along the fiber axis at 24°C of 60 ± 2 GPa and 380 ± 20 MPa, respectively, were achieved by the two-stage draw, because the DRt,max was remarkably higher for this technique than for solid-state coextrusion (DRt,max = 48 vs. 25). The increase in the crystallite size along the fiber axis (D0015), determined by X-ray diffraction, is found to be a useful measure for the development of the morphological continuity along the fiber axis of drawn products.© 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2551-2562, 1998
    Zusätzliches Material: 13 Ill.
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  • 61
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2573-2585 
    ISSN: 0887-6266
    Schlagwort(e): polyethylene ; poly(butylene terephthalate) ; blend ; rheology ; Palierne's model ; morphology ; differential scanning calorimetry ; crystallization ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Crystallization at high supercooling of polybutylene terephthalate (PBT) droplets dispersed in a molten polyethylene (PE) matrix was investigated through rheological and DSC experiments. The Palierne's emulsion model was used as a theoretical framework for studying the viscoelastic behavior of the blends in different ranges of temperature: on the one hand, when the two polymers are molten (T 〉 225°C) and on the other hand, when PBT droplets are at high supercooling in the molten PE matrix (130°C 〈 T 〈 205°C). From rheological experimental evidences it was shown that molten and solidified droplets coexist at high supercooling. The Palierne's model was then successfully adapted to take into account the three phases (molten PE, molten PBT droplets, and solidified PBT droplets). The evolution of the behavior with the temperature is consistent with the growing amount of crystallized droplets. Moreover, a calculation taking into account the droplets size distribution and the number of nuclei is introduced to explain the crystallization behavior of three different blend ratios.© 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2573-2585, 1998
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 62
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2623-2634 
    ISSN: 0887-6266
    Schlagwort(e): interface ; surface tension ; rheological ; morphology ; polymethylmethacrylate ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Impact modifiers with grafted PMMA shell are used to modify polymethylmethacrylate matrix. The composition of the shell is chosen to enhance the interactions at the modifier/matrix interface and to obtain good dispersion of the impact modifier in order to optimize impact strength of the blend. The degree of interactions at the interface is characterized by the interfacial region where the chains of the matrix mix with those of the shell of the modifier. The deviation of the measured viscoelastic behavior of these blends from that predicted by the emulsion models has been attributed to the formation of the network structure due to the association of matrix chains with the shell of the modifier. It is expected that the network structure will decrease with increasing frequency and, as such, the effective volume of the particle is frequency dependent. This study uses the emulsion models to estimate the larger effective volume of the particle and, therefore, the extent of interaction at the interface. In the blends of this study it can be shown that at low modifier levels the solvent swelling of the modifier shell results in stronger interactions with the matrix; this effect is negated by the aggregation of particles at higher modifier loadings. The interaction of core modifier with the PMMA matrix seems to be similar to that of the core-shell modifier. This would not be expected from the calculated interfacial thickness of approximately 4 nm. It is, therefore, proposed that during melt-processing the core modifier surface was altered due to grafting of the matrix PMMA chains during melt-blending to (BA/St) copolymer of the core modifier thus reducing the interfacial tension. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2623-2634, 1998
    Zusätzliches Material: 16 Ill.
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  • 63
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 37 (1995), S. 249-254 
    ISSN: 0959-8103
    Schlagwort(e): poly(ethylene succinate) ; crystallization ; morphology ; electron microscopy ; thermal analysis ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The morphology of melt-crystallized poly(ethylene succinate) (PES) was investigated by optical microscopy and scanning electron microscopy, and the melting behaviour of PES was studied by differential scanning calorimetry (DSC). At low crystallization temperature imperfect crystals were formed which could melt and recrystallize during the DSC scan. Triple melting peaks were observed, and the melting behaviour was strongly dependent on crystallization time and scan rate. It was observed that crystallization at high temperature perfected the crystals (dominant and subsidiary lamellae in the spherulitic structure). Increasing the scan rate reduced the chance for reorganization. However, at high crystallization temperature two melting peaks were observed. The material formed was much more perfect, so that the melting process was not dominated by recrystallization. Accordingly, the cause of dual melting is the existence of two kinds of crystal perfection.
    Zusätzliches Material: 10 Ill.
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  • 64
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 38 (1995), S. 357-362 
    ISSN: 0959-8103
    Schlagwort(e): polyether-copolyester ; morphology ; crystallization behavior ; transparency ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A series of polyether-copolyester segmented copolymers ((PBT-PET)PTMG) based on hard segments of tetramethylene terephthalate-ethylene terephthalate copolyester (PBT-PET) and soft segments of poly(tetramethylene ether)(PTMG) was synthesized. The hard : soft segment weight ratio was 30 : 70 and the mole ratio of PBT : PET was 1 : 10; 1 : 6; 1 : 1; 3 : 1, respectively. Their mechanical properties, morphology, crystallization behavior and optical transparency were investigated and compared with poly(tetramethylene terephthalate)-poly(tetramethylene ether)(PBT-PTMG), as well as with poly(ethylene terephthalate)-poly(tetramethylene ether)(PET-PTMG), consisting of the equivalent composition ratio of hard and soft segments. It was found that the transparency could be improved by introducing a small amount of PBT into PET-PTMG through copolymerization. However, a decrease was observed in the transparency if more PBT was added. This is due to the fact that the copolymerization makes both crystallinity and crystallization rate decrease.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 65
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 38 (1995), S. 367-373 
    ISSN: 0959-8103
    Schlagwort(e): poly(ethylene terephthalate) ; annealing ; thermal behaviour ; morphology ; crystallization ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The influence of annealing conditions on the morphology and melting behaviour of poly(ethylene terephthalate) (PET) was studied. PET annealed under isothermal conditions often shows double melting endotherms depending on the annealing temperature (Ta) and the heating rate of the calorimeter. It was found that the morphological structure and the lower melting peak depend strongly on the annealing temperature, Ta. The increase of the lower melting peak temperature with Ta is due to an increase of the lamellar thickness within the spherulitic structure and to a higher crystallite perfection.
    Zusätzliches Material: 8 Ill.
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  • 66
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 38 (1995), S. 375-380 
    ISSN: 0959-8103
    Schlagwort(e): poly(butylene terephthalate) ; annealing ; thermal behaviour ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A detailed description of the morphology and the complex melting behaviour of poly(butylene terephthalate) (PBT) annealed in the range 80-228°C is presented. Double melting endotherms can be obtained by annealing PBT in a differential scanning calorimeter (DSC). The lower endotherm corresponds to the melting of crystalline material formed at the annealing temperature in addition to some of the crystallized material reorganized during the quenching process. The upper melting endotherm results from the melting of a fraction of the original crystalline material reorganized during the DSC scan. Electron microscopy showed that the spherulitic structure over a wide range of annealing temperature below the melting point is unchanged. At high annealing temperatures, such as 228°C, electron micrographs showed that the narrow high melting peak is associated with the melting of isolated single crystals grown at that temperature.
    Zusätzliches Material: 7 Ill.
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  • 67
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 38 (1995), S. 381-385 
    ISSN: 0959-8103
    Schlagwort(e): poly(vinylidene fluoride) ; crystallization ; thermal behaviour ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The influence of crystallization temperature on the melting behaviour and the morphology of poly(vinylidene fluoride) (PVF2) has been investigated. The DSC endotherms of PVF2 crystallized from the melt show at least two peaks. The peak areas depend on the thermal history of the samples and the heating scan rate. The area of the first peak was found to increase as the crystallization temperature or the scan rate increased. The double peak configuration was attributed to a melting-recrystallization process. Electron microscopy supports these results, for which only one type of lamella was found in the spherulitic structure.
    Zusätzliches Material: 7 Ill.
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  • 68
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 40 (1996), S. 201-205 
    ISSN: 0959-8103
    Schlagwort(e): poly(o-toluidine) ; poly(m-toluidine) ; monomer concentration ; morphology ; polymerization ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Under galvanostatic deposition conditions poly(o-toluidine) exhibits a higher rate of polymerization than poly(m-toluidine). This observation is supported by results obtained by different characterization techniques such as spectrophotometry, scanning electron microscopy and thermogravimetric analysis. The monomer concentration was found to be the predominant parameter in obtaining selectively a conducting salt phase in both cases. However, the morphology of these polymeric films does not reveal any particular relationship with monomer concentration; instead a mixed morphology, i.e. a combination of granules and fibres, is observed. Finally, the thermal stability of poly(m-toluidine) is lower than that of poly(o-toluidine) with a shift of 190°C in the final decomposition temperature.
    Zusätzliches Material: 6 Ill.
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  • 69
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 5 (1995), S. 191-198 
    ISSN: 1057-9257
    Schlagwort(e): TiN ; adhesion ; PVD ; electron shower ; arc ion plating ; sputtering ; wear ; surface ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Elektrotechnik, Elektronik, Nachrichtentechnik , Physik
    Notizen: It has been found that TiN films with high wear resistance and high adhesion can be prepared by electron shower deposition and arc ion plating on glass and austenitic stainless steel (SUS 316) substrates. The high wear resistance is principally explained by the grain size and surface morphology. Fine {100}-faceted crystals (10-150 nm) grew on the surface. The typical morphology of the crystals was triangular pyramidal. The crystallite size was changed by the bias voltage. Faceted crystals produced by arc ion plating were rounded and smoothed by a change in bias, but were unaltered in samples prepared by the electron shower process. The fine faceted surfaces had higher wear resistance than the granularly rounded ones. When TiO2 was formed at the interface of the glass substrate, the adhesion was lowered. The high-adhesion film prepared by electron shower deposition contained a small amount of TiO2 at the interface.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 70
    ISSN: 0959-8103
    Schlagwort(e): polyimide ; m-cresol ; phase structure ; morphology ; phase boundary diagram ; gel/sol transition ; DSC ; polarized light microscopy ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: An organo-soluble aromatic polyimide has been synthesized from 3,3′, 4,4′-bis(phenyltetracarboxylic) dianhydride (BPDA) and 2,2′-bis (trifluoromethyl)-4,4′-diaminobiphenyl (PFMB) via a one-step polymerization in m-cresol. The phase boundary diagram for this system has been established by differential scanning calorimetry, polarized light microscopy (PLM) and wide angle X-ray diffraction (WAXD) experiments. A crystallosolvate form I has been found over the entire concentration region at low temperatures. When the temperature is increased, an isotropic phase has been observed below concentrations of about 40%. In the relatively high concentration region between 45 and 95%, a transition from the crystallosolvate from I to a crystallosolvate form II has been observed. Form II exhibits a different WAXD pattern. In a narrow concentration region between the isotropic and the crystallosolvate form II (40-45%), a biphase behavior has been found. The birefringence of this region may be an indication of a liquid crystalline phase. The BPDA-PFMB polymer crystal has been found in the very high concentration region (〉95%) for temperatures 〉250°C. The morphologies of these phases have been investigated via PLM and transmission electron microscopy. Above the gel/sol transition temperature, the form I shows negative birefringent spherulites consisting of thin lamellae. The form II exhibits a tendency of positive birefringent spherulites. Possible mechanisms of the formation of the metastable phase morphology and their associations with the mechanical gel/sol transition are also discussed.
    Zusätzliches Material: 13 Ill.
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  • 71
    ISSN: 0959-8103
    Schlagwort(e): conducting polymer ; polypyrrole ; poly(heptamethylene p,p′-bibenzoate) ; electrosynthesis ; FTIR ; conductivity ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Polypyrrole-poly(heptamethylene p,p′-bibenzoate) conducting materials, PPy-P7MB/ClO4, were obtained by anodic coupling of pyrrole into a polybibenzoate inert matrix, using perchlorate anions as dopant agent. P7MB is a main-chain liquid crystalline polybibenzoate with adequate mechanical properties and elastic modulus of 1.4GPa at room temperature. The method of synthesis, galvanostatic or potentiostatic electrodeposition, is responsible for differences in the PPy-P7MB/ClO4 films electrochemical response. FTIR spectra show the complex structures of P7MB and the composite conducting material.The conductivity of PPy-P7MB/ClO4 films maintains a relatively high value, σ = 13.74Scm-1, in spite of the insulating effect of polybibenzoate. Film micrographs reveal the typical cauliflower morphology exhibited by polypyrrole and the evolution of film growth with time.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 72
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 39 (1996), S. 55-60 
    ISSN: 0959-8103
    Schlagwort(e): interpenetrating networks ; graft copolymers ; polyurethanes ; allyl novolacs ; dynamic mechanical analysis ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Two series of polyurethane (PU)/allyl novolac resin simultaneous interpenetra ing networks (SINs) were synthesized. The PU components were prepared by reacting 4,4′-diphenyl methane diisocyanate with poly(tetramethylene oxide) (PTMO), whose molecular weight range was 600-700 (for convenience, this polymer was called UT1), 900-1050 (UT2) and 1900-2100 (UT3), respectively. The phenolic resin component was synthesized by substituting the hydroxy groups of the phenolic resin with the allyl group. To prove that the alkene group can be applied as a binding element between the networks to improve the network compatibility, trimethylol propane monoally ether (TMPME) with a double bond was chosen as the PU chain extender in one series of the PU/allyl novolac resin SINs (designated TUT1, TUT2 and TUT3 for different molecular weights of PTMO used as PU soft segments). After a detailed study of the thermal, mechanical, and dynamic properties and morphology, the extent of phase mixing of the graft PU/allyl novolac resin SINs (TUT series SINs) was significantly improved over that of UT series SINs. This result is consistent with the loss tangent shift in dynamic mechanical analysis measurements and with transmission electron microscope micrographs. The mechanical properties of the graft SINs (TUT series) were lower than those of the original SINs (UT series) because TMPME with bulky structure was used as the chain extender of PU.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 73
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 7 (1997), S. 149-156 
    ISSN: 1057-9257
    Schlagwort(e): polyaniline ; synthesis ; surface tension effect ; morphology ; SEM ; ESR ; electrical conductivity ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Elektrotechnik, Elektronik, Nachrichtentechnik , Physik
    Notizen: Polyaniline (PANI) prepared in water or a water-methanol (1:1) mixed solvent by anodic oxidation of aniline hydrochloride at a potential of 0.8 V (and higher) vs. Ag/AgCl appears to form microrods of almost uniform shape and dimensions: a diameter of 0.7 μm and a length of 2-3 μm or more. A surface point contact Pt or Ir electrode has been used as the working electrode to get a better ordering in the product due to the surface tension effect. The structure observed with a scanning electron microscope (SEM) is complex: the sample is highly porous and looks like a coral reef; the average channel diameter is 1.5 and 2.5 μm for narrow and wide channels respectively. The rods appearing in great number in the sample are surprisingly uniform, particularly with respect to the diameter. The electrical conductivity is of the order of 10-1 S cm-1 for most samples examined. The electron spin resonance (ESR) spectra consist of a strong singlet line (g = 2.0030-2.0039, ΔH =;0.12-0.50 mT); similarly, the infrared (IR) spectra show a strong and broad absorption due to electron excitations and electron-lattice interactions, which we have observed previously for many PANI samples examined in our laboratory. © 1997 John Wiley & Sons, Ltd.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 74
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 37 (1995), S. 47-52 
    ISSN: 0959-8103
    Schlagwort(e): poly(butylene terephthalate) ; melting behaviour ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A detailed description of the morphology and the complex melting behaviour of poly(butylene terephthalate) crystallized isothermally from the melt is presented. Triple, double, or single melting endotherms can deliberately be obtained by varying the heating rate in the differential scanning calorimeter (DSC). At low crystallization temperatures, Tc, triple melting endotherms were seen when the specimen was scanned at 10°C/min, while at high Tc a single endotherm was seen. In the case of the triple melting peaks, the first endotherm corresponds to melting of the imperfect crystals formed at the crystallization temperature. The second endotherm originates from melting of the perfect crystals in the initial distribution, and to some recrystallized meterial. The third endotherm is due to melting of the original crystalline material reorganized during the DSC scan. A detailed morphological study of the isothermally crystallized samples by electron microscopy showed that dominant and subsidiary lamellae in the spherulitic structure are related to perfect and imperfect crystals, respectively.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 75
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 41 (1996), S. 227-236 
    ISSN: 0959-8103
    Schlagwort(e): blends ; morphology ; mechanical properties ; electron microscopy ; polypropylene ; ethylene vinyl acetate ; TEM ; SEM ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Several polypropylene-ethylene vinyl acetate (PP/EVA) copolymers with compositions ranging from 90/10 to 10/90 PP/EVA were prepared and characterized in terms of their morphology by transmission and scanning electron microscopy, and their mechanical properties were also studied. The results show a wide range of spatial structures which correlate well to the corresponding measurements of elastic modulus of the blends.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 76
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 7 (1997), S. 195-206 
    ISSN: 1057-9257
    Schlagwort(e): cubic silicon carbide ; morphology ; photoluminescence ; micro-Raman ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Elektrotechnik, Elektronik, Nachrichtentechnik , Physik
    Notizen: Optically transparent cubic SiC crystals were grown via atmospheric-pressure chemical vapour deposition (APCVD) on graphite substrates from methyltrichlorosilane (MTS) in hydrogen in a cold-wall RF induction furnace at temperatures from 1500 to 2000°C. The morphology of the crystals was correlated to substrate temperature, H2/MTS ratio and hydrogen flow. Low-temperature photoluminescence (PL) spectra exhibited a zero-phonon line (2.3787 eV) attributable to an exciton bound to a neutral nitrogen donor, in addition to TA, LA, TO, and LO phonon replicas. The observed broadening and splitting of the PL spectral lines were associated with the morphological habit and internal strain of individual crystallites.Above about 1600°C preferential 〈110〉 growth directions were identified for the majority of the crystals. At intermediate deposition temperatures (1600-1700°C) the dominant morphology consisted of yellow prismatic crystals heavily twinned along {111} and {111¯}. At temperatures of about 1750°C hexagonally shaped {111}-oriented 3C-SiC platelets were formed with alternating {001}/{101} edges. A layer-by-layer growth model was used to rationalise the transition in preferred growth direction from 〈111〉 to 〈101〉 with increasing substrate temperature. © 1997 John Wiley & Sons, Ltd.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 77
    Digitale Medien
    Digitale Medien
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 418-429 
    ISSN: 0142-2421
    Schlagwort(e): AFM ; elastomer ; morphology ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: In order to determine and optimize structure-property relationships in polymer blends, a knowledge of microscopic morphology and physical properties is essential. However, much of this microscopic morphology and physical property information has not been readily available using conventional characterization techniques. In this work, the capability of force modulation atomic force microscopy (AFM) for determining the detailed microstructure and physical properties of industrial polymer blends is evaluated for the first time. When combined with cryogenic facing, force modulation mapping is shown to be a very valuable microcharacterization technique that has a wide range of applicability. The modulus contrast obtained in the analysis of blends and composites allows one to distinguish polymer phases and related morphology with ease and with good specificity. This capability is demonstrated on a variety of filled and unfilled elastomer/plastic and elastomer/elastomer blends. In addition, analyses are successfully performed on a variety of blends containing isobutylene-based polymer that cannot be unambiguously characterized by electron microscopy techniques (isobutylene-based polymers rapidly degrade under electron bombardment). Force modulation mapping is also shown to be quite useful in distinguishing different types of fillers and their distributions in different polymer domains. Moreover, the capability of force modulation mapping for determining microscopic changes in cross-link density is examined. Examples of cross-linking mapping are presented for NR/BIMS, PP/EPDM and BIMS/BR blends. Finally, a semiquantitative calibration of relative force modulation amplitude vs. NR cure state is presented. All of these types of analyses are obtained without a need for the topographical contrast required by conventional AFM techniques and without the need for the complicated and time-consuming etching, staining and cryosectioning (thin films) typically required by electron microscopy techniques. © 1997 John Wiley & Sons, Ltd.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 78
    Digitale Medien
    Digitale Medien
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 837-854 
    ISSN: 0142-2421
    Schlagwort(e): polypyrrole ; toluene sulphonate ; steel ; AFM ; XPS ; morphology ; interface ; corrosion ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: We have characterized electrically conductive polymer, polypyrrole (Ppy), films on mild steel with atomic force microscopy (AFM) and x-ray photoelectron spectroscopy (XPS). The Ppy films were polymerized electrochemically from sodium p-toluene sulphonate (ToS) water-ethanol solution. A very good corrosion protective effect of those films on mild steel has been observed previously. After drying in air, thin Ppy films (∽200 nm) were highly adhesive, whereas thicker films (∽7.5 μm) could easily be peeled off from the metal. All films had a nodular surface structure. Thin films were very smooth and their roughness increased with their thickness. The AFM study of the interface between the metal and the polymer showed areas of different morphology, which suggests that adhesive and cohesive failure of the polymer film occurs. A strong variation of the chemical composition at the interfacial layer was observed. A sulphur-rich layer was formed at the interface, indicating that the counter-anions (ToS) were accumulated on the surface of the metal. High-binding energy iron and imine-type nitrogen were detected in a thin Ppy film. Moreover, thin films were substantially overoxidized. The number of anions incorporated into the Ppy matrix varied as a function of film thickness: the ‘doping level’ was about 30% for thicker films and only 12% for thin ones. Nitrate counter-anion-containing Ppy films were also studied in some cases for comparison. © 1997 John Wiley & Sons, Ltd.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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