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  • 1
    ISSN: 0935-9648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 20 (1993), S. 1061-1066 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A GaAs/AlAs superlattice growth by metal-organic chemical vapour deposition is being proposed as the single crystalline multilayer reference material for sputter depth profiling. This material was characterized by transmission electron microscopy experiments, which showed that the interface between GaAs and AlAs is atomically flat. The preliminary depth profiling experiments were carried out by AES and SIMS.The AES experiments were performed using a Perkin-Elmer SAM 660 scanning Auger microprobe and the SIMS experiments were carried out using a VSW multitechnique XPS/SIMS surface analysis system.The AES and SIMS sputter depth profiling experiments proved that the depth resolution was found to be almost constant for each interface when an Ar+ beam was used for sputtering. Therefore the sputtering-induced roughness is very small for this material with Ar+ beam profiling, the depth resolution deteriorated as a function of depth, indicating oxygen ion beam-induced surface roughening.For both AES and SIMS, the depth resolution improved for ion beams with lower kinetic energy and more glancing angles of incidence.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 23 (1995), S. 851-857 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Because the chemical states of the elements in SrTiO3 thin film on Si are reduced by argon ion beam bombardment, it was impossible to sputter depth profile the chemical states of SrTiO3 thin film by argon ion beams. In this paper, it is reported that the undistorted chemical states of Ti and Si at the SrTiO3/Si interface can be determined with oxygen ion beams at the appropriate 70° angle of incidence, with which either metallic Ti is not oxidized or Ti in SrTiO3 is not reduced. Under the sputter depth profiling conditions, the chemical state of Ti at the SrTiO3/Si interface could be successfully characterized and the effects of post-annealing at high temperature on the chemical state of Ti were studied. A significant number of Ti atoms in the metallic state were observed at the SrTiO3/Si interface without any post-annealing but all of them were oxidized to the Ti4+ chemical state after 2 h post-annealing at the temperatures above 600°C under oxygen flow. The dielectric properties of SrTiO3 thin films on Si were well correlated to the oxidation state of Ti and the broadening of the interface SiO2 layer induced by post-annealing at high temperature.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 95-103 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Measurements were taken of the viscoelastic properties of six polymer melts by mean of the Weissenberg rheogoniometer and the Han slit/capillary rheometer. Polymers in vestigated were three high-density polyethylenes of different polydispersity, a low-density polyethylene, a polypropylene, and a polystyrene. The range of shear rates tested was from about 5.0 × 10-3 to 10 sec-1 with the Weissenberg rheogoniometer, from about 10 to 102 sec-1 with the slit rheometer, and from about 102 and 103 with the capillary rheometer: the temperature of measurement was 200°C. The three different apparatuses give consistent results over almost six decades of shear rates, yielding satisfactory correlations of shear viscosity to shear rate and of normal stress difference to shear rate.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 2477-2482 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Careful examination of x-ray diffraction patterns from melt-crystallized nylon 11 films show significant discrepancies with the proposed α-form structure. These discrepancies do not disappear after the samples have been annealed. The temperature dependence of the d spacings of the two strongest peaks show further evidence that the melt-crystallized and solution-cast films (α form) possess different crystal structures. These results suggest a different crystal structure for the melt-crystallized films; this would help explain the rather low piezoelectric response of these films and also the failure to observe a rapid decrease in polarization at the transition temperature.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1755-1765 
    ISSN: 0887-624X
    Keywords: 1-(trifluoromethyl)-2,3,5,6-benzenetetracarboxylic dianhydride ; amide acid ; poly(amic acid) ; isomeric unit ; nuclear magnetic resonance spectroscopy ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two different poly(amic acid)s were synthesized by the polycondensations of 1-(trifluoromethyl)-2,3,5,6-benzenetetracarboxylic dianhydride (CF3DAN) with p-phenylene diamine and benzidine. In addition, an amide acid model compound was prepared from CF3DAN and aniline. Isomeric units in the poly(amic acid)s as well as the amide acid were investigated by 1H and 13C-nuclear magnetic resonance (NMR) spectroscopies. Spectroscopic results indicate that the major isomeric component was a CF3-meta-isomeric unit centered on the aromatic carbon substituted with the trifluoromethyl group. In particular, the amide acid compound was determined to be composed of 80 mol % CF3-meta-isomer and 20 mol % H-meta-isomer. Therefore, for the poly(amic acid)s, the minor isomeric component is speculated to be a H-meta-isomeric unit rather than a para-isomeric unit. The result might result mainly from the strong electron-withdrawable and bulky trifluoromethyl substituent in the CF3DAN monomer. The strong electron withdrawability might significantly enhance the reactivities of the adjacent carbons in the monomer to the nucleophilic attack of the amino nitrogen in the aniline and diamines, and consequently overcome the role of the bulkyness, ultimately leading to the amide acid and poly(amic acid)s rich with the CF3-meta-isomeric unit. In addition, a portion of the imide form was detected in the dried AN-CF3DAM-AN amide acid. Thus, the formation of imide linkage might be involved in a small portion for the dried poly(amic acid)s. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1755-1765, 1998
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 1 (1990), S. 263-273 
    ISSN: 1042-7147
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Small-angle neutron scattering studies have been used to clarify several aspects of the internal structure of latexes and subsequent film formation modes. This paper reviews work both around the world and at Lehigh University on those subjects. Two points have been made clear: (1) The appearance of core-shell phenomena in latexes depends on the size of the polymer chain to that of the latex particle; the phenomenon is most marked when the radius of gyration of the chain is about one fifth as big as the latex radius. (2) Strength build-up during film formation depends on the extent of interdiffusion of the chains. For moderate molecular weights, interdiffusion distances of one radius of gyration yield maximum strength. For both moderate (250,000 g/mol) and high (2,000,000 g/mol) molecular weights, full strength was achieved in two hour's annealing time at 144°C.
    Additional Material: 11 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 26 (1995), S. 263-268 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Qn the viscosity of glass melts and porous sintered glassesSuspensions of solid phase particles in molten glasses modify their flow behavior and therefore their viscosity. This work deals with the dependence of the effective viscosity (ηeff) of isotropic suspensions on the concentration of the solid phase particles. Independently of the shape of the inclusions the values of the effective viscosities lie between upper [ηeff = ηL (1 - CD)-14 ]and lower bounds [ηeff = ηL (1 - CD)-3], where ηL is the viscosity of the molten glass and CD is the volume fraction of solid inclusions. The lower bound is also valid for the effective viscosity of suspensions containing spherical inclusions.Pores present in a glass matrix affect its flow behavior and consequently its creep and sintering behavior. The effective viscosity of porous glasses (ηP) as a function of the volume fraction of pores, or porosity (P), also varies between and upper [ηP = ηM (1 - P)1.04] and a lower bound [ηP = ηM (1 - P)14], where ηM is the viscosity of the nonporous glass matrix. For spherical porosity the equation is: \documentclass{article}\pagestyle{empty}\begin{document}$${\rm \eta_P = \eta_M(1 - P)^{1.5}}$$\end{document}Measured values for the viscosity of different suspensions as reported in the literature as well as own experimental data on two glass-solid systems are compared with the theoretical values predicted by these equations. In a similar way literature data for the viscosity of porous sintered glasses are compared with the respective equations. In all cases a fair agreement between experiment and theory was found in some cases the agreement was excellent. Therefore the presented equations constitute a reliable approach for the prediction of the viscosity of suspensions and porous sintered glasses and since they do not contain fitting parameters, they are of substantial practical relevance (for a comprehensive english treatment of the matter compare Glastechnische Berichte, Proc. Otto-Schott-Colloquium 1994).
    Notes: Suspensionnen von Festphasenteilchen in Glasschmelzen verändern deren Fließverhalten und damit deren Viskosität. Die vorliegende Arbeit behandelt die Abhängigkeit der effektiven Viskosität (ηeff) isotroper Suspensionnen von der Konzentration der Festphansenteilchen. Unabhängig von deren Form liegen die effektiven Viskositäten zwischen oberen und unteren Grenzwerten, deren Konzentrationsabhängigkeit durch Näherungslösungen gegeben ist: obere Grenzwertgleichung: ηeff = ηL (1 - CD)-14untere Grenzwertgleichung: ηeff = ηL (1 - CD)-3(ηL = Viskosität der Schmelze; CD = Volumenanteil der Festphasenteilchen). Für die effektive Viskosität von Suspensionen mit sphärischen Festphasenteilchen gilt die untere Grenzwertgleichung.Poren in Sintergläsern verändern ebenfalls deren Fließ- und damit Sinter-, Umform- und Kriechverhalten. Die effektive Viskosität poröser Gläser (ηP) als Konzentrationsfunktion ist gegeben durch die Näherungslösungen: obere Grenzwertgleichung: ηP = ηM (1 - P)1.04untere Grenzwertgleichung: ηP = ηM (1 - P)14(ηM = Viskosität des porenfreien Glases; P = Porosität).IM Falle sphärischer Porosität gilt die Viskositätsgleichung \documentclass{article}\pagestyle{empty}\begin{document}$${\rm \eta_P = \eta_M(1 - P)^{1,5}}$$\end{document}Gemessene Werte der Viskosität diverser Suspensionen sowie von Na2O-SiO2-Schmelzen mit dispergierten festen SiO2-Teilchen und Na2O-GeO2-Schmelzen mit dispergierten GeO2-Teilchen werden ebenso mit berechneten Werten verglichen wie die experimentellen Werte der Viskosität von porösen Sintergläsern mit den entsprechenden theoretischen. In allen Fällen wurde hinreichende, vielfach beste Übereinstimmung festgestellt. Die Gleichungen liefern praxisrelevante, verläßliche Aussagen sowohl für Suspensionen wie für poröse Sintergläser.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Advanced Materials 8 (1996), S. 928-932 
    ISSN: 0935-9648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 305-322 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The dynamic mechanical properties of polymeric composites composed of crosslinked poly(n-butyl methacrylate) continuous-phase and crosslinked polystyrene dispersed phase with poly(n-butyl methacrylate) occlusion have been examined. The composite samples were prepared by mixing and swelling of the crosslinked polystyrene particles obtained by emulsifier-free emulsion polymerization, with n-butyl methacrylate and crosslinker, then photopolymerizing at the desired temperature. The composite microstructure was varied by either changing the crosslink density of polystyrene, and temperature of swelling and polymerization, or using different sizes and contents of polystyrene particles. The tan δ peak positions of composite samples are found to be dependent on morphological characteristics as well as the properties of the dispersed phase while the peak height seems to be dependent on the effective volume of dispersed phase composed of polystyrene and poly(n-butyl methacrylate) occlusions. Special attention has been paid to the comparison among composite, homonetworks, and bulk IPN samples that are expected to have the identical structure with the complex dispersed phase of the composite samples. © 1993 John Wiley & Sons, Inc.
    Additional Material: 21 Ill.
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