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  • Polymer and Materials Science  (46)
  • Crystal Structure  (20)
  • 1990-1994  (66)
  • 1
    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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  • 2
    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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  • 3
    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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  • 4
    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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  • 5
    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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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 44 (1992), S. 1043-1049 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Urethanes of cellobiose and cellulose-containing uretdione groups are synthesized by the reaction of aliphatic and aromatic diisocyanate uretdiones with the saccharides. The syntheses are performed as a heterogeneous reaction in dimethyl acetamide using dibutyl tin dilaurate as a catalyst, as well as a homogeneous reaction in dimethyl acetamide-lithium chloride. Thus, Semisynthetic prepolymers are formed that offer the reactivity of (blocked) isocyanate groups. To demonstrate their reactivity, ring opening of the uretdiones is performed by the addition of a secondary amine to yield the corresponding ureas.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 1183-1188 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Classically, the one-step synthesis of interpenetrating polymer networks (IPNs) and related materials requires noninterfering polymerization modes to achieve distinct networks, held together by only physical entanglements. For the combination of (meth) acrylic and allylic monomers, both polymerizable by free radicals, a new in situ sequential synthesis for obtaining semi-IPNs is proposed. Using specific initiators that decompose at two different temperatures, refractive index measurements, Fourier transform infrared spectroscopy, and dynamic mechanical analysis have shown that neat species are formed and that the two monomers do not copolymerize. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 28 (1994), S. 1221-1231 
    ISSN: 0021-9304
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin , Technik allgemein
    Notizen: Fiber/matrix interfacial bond strength significantly influences the mechanical behavior of fiber-reinforced polymer (FRP) composites. Interfacial bond strength durability is therefore particularly important in the development of FRP composites for implant applications where diffused moisture may potentially weaken the material over time. In this study, the long-term durability of interfacial bonding in carbon fiber/380 grade polyetheretherketone (C/PEEK) and carbon fiber/polysulfone (C/PSF) composites was investigated after exposure to hygrothermal environments. A single fiber pull-out test was used to quantitatively determine the ultimate bond strength (UBS) of the samples following exposure. Samples were tested at three temperatures (37, 65, and 95°C) for six time periods (0-5000 h) and in two environments (dry and physiologic saline-immersed). A mathematical model based on nth order chemical reaction kinetics was applied to describe the long-term durability of the interface. The results of this study indicate that interfacial bond strengths in C/PSF and C/PEEK (380 grade) composites are significantly decreased by exposure to physiologic saline and are functions of both time and temperature. For each material, the kinetics of degradation analysis predicts further bond strength losses following initial saturation, which then stabilizes at temperature-dependent equilibrium bond strength levels. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In this paper photocurrents of N-isopropylcarbazole (NIPC) derivatives in polycarbonate hosts are reported and compared to data for a benzotriazole derivative (BTA). The carbazole moiety was substituted with both electron donor and acceptor substituents and the photoconductivity was measured as a function of concentration, electrical field, and temperature using the time-of-flight (TOF) technique. The observed increase of the effective mobility of charge carriers at low dopant concentrations upon substitution with a moderate electron acceptor is in contrast to literature data for some other materials. We interpret this increase as being due to an increase in the delocalisation radius of the transport state of the substituted carbazole molecule. The field dependence of the effective mobility shows Poole-Frenkel behaviour, which is attributed to polaron formation. Comparison of the effective mobility of the NIPC derivatives with BTA shows that the size of the molecule plays a decisive role for the absolute value of the effective mobility.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 1237-1248 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Ethyl p-vinylbenzenesulfonate (ESS) for which a new synthesis is described has been copolymerized with vinylcarbazole, styrene, p-methylstyrene and p-bromostyrene in N,N-dimethylformamide at 60°C using azoisobutyronitrile as initiator. Copolymer compositions and copolymerization parameters have been evaluated. Q, e-values for ESS are 4,19 and -0,11. Thermal properties of the copolymers have been investigated by differential scanning calorimetry and thermogravimetric analysis. Polyelectrolytes have been prepared either by polymer analogous hydrolysis of the sulfonic acid esters followed by conversion of the free acids into alkali metal salts or by using the alkylating properties of the esters towards tertiary amines or pyridines to form the appropriate sulfonic acid ammonium or pyridinium salts. The latter method offers the opportunity to synthesize polyelectrolytes with a well defined content of chromophores.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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