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  • Polymer and Materials Science  (66)
  • Crystal Structure  (40)
  • 1995-1999  (40)
  • 1990-1994  (66)
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  • 1
    ISSN: 0935-9648
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 29 (1991), S. 555-570 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Modification of fluorine-containing polymers has recently received much attention due to new chemistries allowing for refunctionalization of these materials, especially their surfaces. In this article results are discussed which demonstrate various interesting modifications (including incorporations of —OH and oxygen comprised functionality) to expanded poly(tetrafluoroethylene) (ePTFE) surfaces. This is effected through the use of low damage, radio frequency glow discharge (RFGD) processes. The low damage conditions, which preserve the original pore structure/morphology of these RFGD treated materials, are supported by Scanning Electron Microscopy (SEM) while the resulting atomic and molecular effects are investigated through other surface analytical methodology. All materials reported in this investigation have been subjected to intensive structural analyses utilizing Electron Spectroscopy for Chemical Analysis (ESCA), Attenuated Total Reflectance Fourier Transform Infrared spectroscopy (ATR-FTIR), and wettability profiles obtained through contact angle measurements using a large series of liquids having varying surface tensions and surface reactive functionality. Through this multitechnique analysis of both expanded PTFE and poly(vinylidene fluoride) (PVDF) treated surfaces, a model is supported which illustrates surfaces possessing both high and low energy regions comprising both oxygen and fluorine functionality in close molecular proximity.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Recent work in our laboratories has fully characterized the surface region of a segmented poly(ether-urethane) (PEU) extending from the air/polymer interfacial region through bulk depths in the micron range. This characterization utilized energy and angle dependent Electron Spectroscopy for Chemical Analysis (ESCA), Attenuated Total Reflectance-Fourier Transform Infrared Spectroscopy (ATR-FTIR), and Comprehensive Wettability Profiling (contact angle using a homologous series of liquids) as defined by Zisman. In this study this same multi-analytical-technique approach is used to elucidate changes in these PEU surfaces induced through an H2O Radio Frequency Glow Discharge (RFGD) plasma. This investigation reports both qualitative and quantitative changes due to the modification treatments as well as the permanency of the changes effected on these surfaces through the plasma treatment. From our analyses, the amount of surface residing polyurethane (hard segment) is observed to increase due to a proposed plasma etching mechanism. Further, the addition of oxygen containing functionality is detected at the modified surfaces unique with respect to the unmodified PEU. These surface modifications which show large increases in wettability, are finally observed to be semi-permanent over a time period of 6 months.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 2141-2149 
    ISSN: 0887-624X
    Schlagwort(e): polyimides ; 4-phenylethynylphthalic anhydride ; thermooxidative stability ; high-temprature MAS NMR ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The synthesis of high glass transition temperature (Tg 〉 300°C), amorphous, soluble, poly-imide oligomers of controlled molecular weight endcapped with 4-phenylethynylphthalic anhydride endcapping agent is described. The 4-phenylethynylphthalic anhydride was employed to afford a higher curing temperature (380-420°C) which widens the processing window compared to unsubstituted acetylene-endcapped polyimides. The polyimides were synthesized via solution imidization techniques, using the ester-acid of various dianhydrides and aromatic diamines. A “ one-pot” procedure utilizing NMP as the solvent and o-dichlo-robenzene as the azeotroping agent reproducibly produced fully imidized, but yet soluble wholly aromatic polyimides. Thermally cured samples were prepared with gel contents of up to 98% that displayed good solvent resistance. Glass transition temperatures comparable to high molecular weight linear analogs were produced. These polyimides also show excellent thermal stability as judged by thermogravimetric analysis (TGA). Model phenylethynyl imide compounds were synthesized and used to follow and elucidate the nature of the products formed from the phenylethynyl curing by using high temperature magic-angle 13C nuclear magnetic resonance (MAS NMR). Preliminary results indicate that the cure reaction can be followed by MAS NMR. However, the nature of the products being formed during the curing process is difficult to determine by the solid-state MAS NMR alone. Differential scanning calorimetry (DSC) data clearly show that the model system does indeed melt and displays a wide window before the strong cure exotherm is observed. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    ISSN: 1042-7147
    Schlagwort(e): interpenetrating polymer networks ; kinetics ; phase separation ; X-ray scattering ; light scattering ; polyurethane ; polystyrene ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Phase separation that takes place during the formation of semi-interpenetrating polymer networks based on crosslinked polyurethane and linear polystyrene was studied by small-angle X-ray scattering and light scattering. The kinetics of the chemical reactions was followed by Fourier transform infrared spectroscopy. The occurrence of broad peaks in the X-ray scattering curves was interpreted in terms of distances between the urethane crosslinks. Small modulations on these curves were assigned to sphere-like structures with a diameter of around 5 nm which might be related to the urethane crosslink regions. Small modulations on the light-scattering curves at the beginning of styrene polymerization were assigned to spheres with diameters of around 4.5 μm, which can be related to the polystyrene-rich phase. These modulations disappear with time, which might indicate an increasing polydispersity of the domain sizes. The final morphology was found to depend on the time at which polymerization of styrene is initiated with respect to the time of gelation of polyurethane.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 6 (1996), S. 239-244 
    ISSN: 1057-9257
    Schlagwort(e): molecular semiconductors ; organic semiconductors ; phthalocyanines ; conductivity ; thermopower ; seebeck effect ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Elektrotechnik, Elektronik, Nachrichtentechnik , Physik
    Notizen: By changing the chemical composition of phthalocyanine molecules, the electrical properties of the ensemble in the solid state can be influenced directly. This is shown for phthalocyaninatomanganese (PcMn) as compared with purely divalent central metals and for complexes in which the ligand system has been modified by either electron-withdrawing heteroatoms such as N instead of CH leading to tetrapyridotetraazaporphyrinatozinc (TPyTAPZn) or substituents such as F instead of H leading to hexadecafluorophthalocyaninatozinc (F16PcZn). The accessibility of additional oxidation states of Mn or the stabilisation of frontier orbital states by the ligand leads to a lower ionisation potential and interactions with impurities or dopant molecules are changed. A change in the observed majority carrier (n-type behaviour) is seen even under UHV conditions. Measurements of the thermoelectric power and electrical conductivity are presented of the pure films and after exposure to oxidising ambient. During film growth either island growth or a growth following the Stranski-Krastanov mechanism was observed. The comparison of the temperature dependence of thermopower and electrical conductivity leads to a discussion of the type of majority carriers, their generation as well as their transportation. For the materials investigated in this study the band model fails to explain the observed properties and a localised transport mechanism has to be considered. A transport in localised states close to the Fermi edge is discussed for TPyTAPZn and F16PcZn.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    ISSN: 1042-7147
    Schlagwort(e): LBK films ; alternating layers ; ionenes ; NLO chromophores ; surface plasmon spectroscopy ; X-ray reflection and diffraction ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Langmuir-Blodgett-Kuhn films of ionene polymers and nonlinear optically (NLO) active amphiphiles were investigated using several ultrathin film-sensitive techniques to determine multilayer ordering. Studies involved the formation of “passive-active” AB y-type multilayers of the ionenes and the NLO active amphiphiles. Deposition was possible with the use of an alternate three compartment dipping trough. The multilayer structures and thicknesses were verified by X-ray diffraction and reflection measurements and surface plasmon spectroscopy on a gold-coated glass substrate. Two main factors were determined to be responsible for the formation of stable alternating film architectures, namely electrostatic interaction in the hydrophilic layers and the van der Waals interaction in the hydrophobic layers. The use of ionenes as a class of amphiphilic polymers allowed the preparation of films with excellent optical quality.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 4 (1993), S. 164-171 
    ISSN: 1042-7147
    Schlagwort(e): Polyelectrolytes ; Glass transition ; Conductivity ; NMR ; Dielectric ; Relaxation ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Ionene glasses are considered as being a new class of materials. Their properties have been investigated in detail by thermoanalytical, solid state NMR, and dielectric techniques. The segmental dynamics of these cationic polyelectrolytes, labeled in chosen positions, have been studied with solid state 2H-NMR. Below the glass transition the quaternized ammonium groups in the polymer backbone are essentially static, due to strong Coulomb interactions. The glass transition in these materials is characterized by the softening of a network formed by the N+-cations. However, both the low molecular weight counterions and the organic chain segments linking the ammonium groups are already mobile below Tg. The dynamics of the organic segments in the glassy state can be described as motion between fixed ends. Ionic conductivity in the glassy state is based on thermally activated anion transport. The influence of the flexibility of the organic chain segments and of the type of the anion on the conductivity are discussed. A simple analytic expression is proposed to describe the conductivity behavior in the low frequency limit.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 3 (1994), S. 223-232 
    ISSN: 1057-9257
    Schlagwort(e): CdTe ; ZnTe ; Impurities ; Spin resonance ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Elektrotechnik, Elektronik, Nachrichtentechnik , Physik
    Notizen: We present results of electron paramagnetic resonance (EPR) and optical spectroscopy on different charge states of the transition metal impurity iron in ZnTe and CdTe. We identify the energy level position of the Fe+ acceptor in ZnTe at Ev + 1.7eV and estimate its position in CdTe. Ionisation transitions from Fe+to the conduction and valence bands ar found in both absorption spectroscopy and photo-EPR. Optical intra-defect tracsitions from Fe+ to crystalfield-split excited states ar resolved for the first time. This assignment to Fe2+ is based on optically detected EPR. Application of both far-infrared Fourier transform and EPR spectroscopy allows the determination of the total iron concentration in all charge states.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 2247-2253 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The physical characterization of hydroxypropylcellulose-indomethacin grafts (HPC-IND) is described. Using size-exclusion chromatography (SEC) and serial differential refractive index (dRI) and ultraviolet spectrophotometric (UV) detection methods, it was possible to characterize the chemical substitution of the HPC-IND graft. Using the acid chloride of IND as the reactive intermediate, the HPC-IND graft was synthesized. The amount of IND grafted onto the polymer as a function of the HPC molecular weight (MW) was then quantitatively estimated. It was found that the substitution of IND onto the HPC was not uniform, representing chemical heterogeneity of the first kind. Increasingly higher substitution (of IND to HPC) was observed as the MW decreased (〈250,000 Daltons) for the HPC backbone. Lower, more uniform substitution was observed for the higher molecular weight regions of the HPC (〉250,000 Daltons). Possible contributing factors affecting the observed nonuniform substitution include (1) the chain coiling of the HPC in solution, thus limiting the availability of the pendant hydroxyl groups, (2) nonuniform substitution of the hydroxypropyl moiety onto the cellulose backbone, and (3) steric effects resulting from the incorporation of the bulky aromatic drug molecule onto the backbone HPC.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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