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  • Polymer and Materials Science  (17)
  • Life and Medical Sciences  (4)
  • Chronic antidepressant  (2)
  • 11
    Electronic Resource
    Electronic Resource
    Decomposition kinetics of a phenolic-carbon composite. II. Rate relationships (1971)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 91-103 
    Details
    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 isothermal decomposition of a phenolic resin in a phenolic-carbon cloth composite was measured in air at 0.1 to 0.2 torr over the temperature range 104-718°C. Two decomposition rate relationships are presented that can be used to predict decomposition. One assumes two second-order consecutive rate-controlling reactions, and the other assumes a diffusion-limited second-order reaction. Two rate constants govern each relationship, one being operative during the initial decomposition stages, and the other during the final stages. Evidence is presented to support the applicability of both relationships to predict decomposition over the entire temperature range studied. Arrhenius plots of the rate constants consist of several segments linearly connected. Activation energies and frequency factors computed from these segments cover a broad range of values. The activation energies are used to correlate the temperature ranges with the predominant products formed in these ranges.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1971.070150108
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  • 12
    Electronic Resource
    Electronic Resource
    Functionalized polyacetals, 1. Copolymerization of trioxane with 1,3-dioxep-5-ene and properties of the resulting copolymer (1990)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 191 (1990), S. 99-105 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 1,3,5-Trioxane (1) and 1,3-dioxep-5-ene (2) were copolymerized with BF3OEt2 at 65°C. The products, after base hydrolysis, were characterized by 13C and 1H NMR and were found to assume the chemical structure 4 of a copolymer containing oxymethylene and oxy-2-butenylene units with 4-hydroxy-2-butenyl and methoxy end groups, with the ratio of hydroxy-2-butenylene to methoxy end groups varying with experimental conditions. The copolymer demonstrates crystallinity and thermal stability comparable to poly(trioxane-co-ethylene oxide)s. Copolymer melting point was observed to decrease with increasing comonomer incorporation. The upper limit for incorporation of the comonomer 2 was found to be ca. 4 mol per cent. Viscosity and end group analysis (by 1H NMR) indicate molecular weights in the range of 104 to 105. The comonomeric unit demonstrates the ability to act as both a stopper against unzipping and as a trap for certain degrading agents.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1990.021910108
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  • 13
    Electronic Resource
    Electronic Resource
    Der mechanische Verwendungsbereich von Werkstoffen (1950)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 1 (1950), S. 51-52 
    Details
    ISSN: 0947-5117
    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
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/maco.19500010202
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  • 14
    Electronic Resource
    Electronic Resource
    Kolloidchemisches Praktikum von E. Sauer. 2. Aufl. Verlag für angewandte Wissenschaften. Wiesbaden 1953. XIII, 122 S., geb. DM 9,80 (1954)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 5 (1954), S. 359-359 
    Details
    ISSN: 0947-5117
    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
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/maco.19540050830
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  • 15
    Electronic Resource
    Electronic Resource
    Ultrafine particles (The electrochemical society series). W. E. Kuhn, H. Lamprey und C. Sheer. John Wiley & Sons Ltd., London 1964, 561 Seiten, Preis sh 113/ -  (1964)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 15 (1964), S. 700-701 
    Details
    ISSN: 0947-5117
    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
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/maco.19640150815
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  • 16
    Electronic Resource
    Electronic Resource
    Phasen-Grenzlinien, insbesondere in ihrer Bedeutung für die Korrosion (1951)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 2 (1951), S. 365-367 
    Details
    ISSN: 0947-5117
    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: Phase boundary-lines, especially in their impotance for corrosionTwo phases have a common cleavageplane, whilst three phases touch one another along a boundary line only. Corroesponding to an adsorption in the first case in an adlineation in the second case. Both processes diminish the free energy and herewith the activity of the boundary, so inhibiting the possibilities of corrosion.Local elements, glow cathodes and catalysts consisting of several components are typical systems acting at microscopic boundary-lines. Cavitation is the inverse phenomenon.Macroscopic boundary-lines in partially filled containers, formed by wall, liquor and gaseous phase, are about this especially active, as being mixed with a four-phases-point-system, that results from the heterogeneity of the container wall. Gravity potentials, and electrokinetic potentials have their maximum value in the boundary-lines too.
    Notes: Zwei Phasen haben eine gemeinsame Grenzfläche, während drei Phasen sich nur entlang einer Grenzlinie berühren. Der Adsorption im ersten Falle entspricht eine Adlineation im zweiten Falle. Beide Vorgänge setzen die freie Energie und damit die Aktivität der Grenze herab, hemmen also Korrosionsmöglichkeiten.Lokalelemente, Glühkathoden und Mehrstoff-Katalysatoren sind typische Systeme, die an mikroskopischen Grenzlinien zur Wirkung kommen. Kavitation bildet die inverse Erscheinung hierzu.Makroskopische Grenzlinien an teilgefüllten Behältern, die durch Wandung, flüssigem Inhalt und gasförmiger Phasegebildet werden, sind darüber hinaus besonders aktiv, da sie von einem Vierphasen-Punktsystem durchsetzt sind, das infolge er heterogenität der Behälterwand resultiert.Gravitationspotentiale und elektrokinetische Potentiale haben ebenfalls in den begrenzenden Linien ihren maximalen Wert.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/maco.19510021004
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  • 17
    Electronic Resource
    Electronic Resource
    Über die Oberflächenenergie fester Werkstoffe (1954)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 5 (1954), S. 208-212 
    Details
    ISSN: 0947-5117
    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: The Surfaces Energy of Stable MaterialsAn explanation of the basic meaning and importance of interfacial surface forces in the building up of materials is followed by an examination of the manysided relations between the surface energy and the other properties of solid materials. The relationships between the tensile strength and other mechanical values, the importance of capillary pressure in active fillers and in separation hardening, the place of synthetic materials in the “Paracher Diagram”, their relation to the specific entropy and others factors are examples of this. Some actual numerical values for surface tension of metals in the solid state, inorganic compounds and synthetic materials are mentioned. However, most of these values depend on empirical methods of calculation.
    Notes: Nach einer Darlegung über die grundsätzliche Bedeutung der Grenzflächenkräfte für den Aufbau der Stoffe wird auf die vielseitigen Bezichungen zwischen Oberflächenenergie und anderen Eigenschaften kompakter Materie eingegangen. Zusammenhänge mit der Zerreißfestigkeit und anderen mechanischen Güteziffern, Bedeutung des Kapillardruckes bei aktiven Füllstoffen und bei der Ausscheidungshärtung, die Lage der Kunststoffe im „Parachor-Diagramm“, ihre Beziehung zur spezifischen Entropie u. a. sind Beispiele hierfür. Ferner werden Zahlenwerte für die Oberflächenspannung im festen Zustand von Metallen, anorganischen Verbindungen und Kunststoffen angeführt, die auf verschiedenen meist empirischen Berechnungsverfahren beruhen.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/maco.19540050603
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  • 18
    Electronic Resource
    Electronic Resource
    Interaction of endothelial cells with a laminin A chain peptide (SIKVAV) in vitro and induction of angiogenic behavior in vivo (1992)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 153 (1992), S. 614-625 
    Details
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Endothelial cells are known to bind to laminin, and two peptides derived from the laminin A (CTFALRGDNP) and B1(CDPGYIGSR) chains block the capillary-like tube formation on a laminin-rich basement membrane matrix, Matrigel. In the present study, we have used various in vitro and in vivo assays to investigate the angiogenic-biologic effects of a third active site in the laminin A chain, CSRARKQAASIKVAVSADR (designated PA22-2) on endothelial cells. The SIKVAV-containing peptide was as active as the YIGSR-containing peptide for endothelial cell attachment but was less active than either the RGD-containing peptide or intact laminin. Endothelial cells seeded on this peptide appeared fibroblastic with many extended processes, unlike the normal cobblestone morphology observed on tissue culture plastic. In addition, in contrast to normal tube formation on Matrigel, short irregular structures formed, some of which penetrated the matrix and sprouting was more apparent. Analysis of endothelial cell conditioned media of cells cultured in the presence of this peptide indicated degradation of the Matrigel and zymograms demonstrated active collagenase IV (gelatinase) at 68 and 62 Kd. A murine in vivo angiogenesis assay and the chick yolk sac/chorioallantoic membrane assays with the peptide demonstrated increased endothelial cell mobilization, capillary branching, and vessel formation. These data suggest that the -SIKVAV-site may play an important role in initiating branching and formation of new capillaries from the parent vessels, a behavior that is observed in vivo in response to tumor growth or in the normal vascular response to injury. © 1992 Wiley-Liss, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jcp.1041530324
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  • 19
    Electronic Resource
    Electronic Resource
    A diffusivity approach for studying polymer structure (1958)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 28 (1958), S. 129-150 
    Details
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Study of the diffusion in polymers of molecules comparable in size and structure to the segments of the chain molecules is suggested as a means of securing information on structure and molecular friction forces in polymers. A convenient method for measuring the diffusivity in polymers of such compounds tagged with C-14 was devised and used to study the diffusivity of octadecane, octadecanol, stearic acid, and octadecyl stearate for a range of temperatures in polymers including natural rubber, GR-S, polybutadiene, polyisoprene, and polyisobutylene. Diffusivities were independent of concentration for the range used. The diffusivities of straight chain hydrocarbons in natural rubber appear to vary inversely as the molecular weight of the diffusing compound. Evidence was found for association effects in the diffusion of stearic acid in natural rubber. Activation energies for diffusion of the compounds were quite similar in any one polymer and of the same order as reported for low molecular weight hydrocarbons and for viscous flow. Larger differences in activation energies were observed for diffusion in the different polymers. Correlations were observed for the diffusivities of octadecane in a series of polymers with their densities and thermal expansivities, especially the latter. Some study was given to the effect on the diffusivity of octadecane of such parameters as polymer unsaturation, solution viscosity, molecular weight, and crosslink density. The diffusivity of octadecane in natural rubber had a pronounced maximum as a function of crosslink density, coinciding with the maximum in tensile strength. Possible implications of this are discussed. The diffusivities of octadecane in a series of elastomers were studied in relation to the internal frictional losses observed for 60 cps vibrations over a range of temperatures. It was concluded that frictional forces deduced from the diffusivity measurements have some correspondence to high frequency viscoelastic phenomena which involve small units of structure comparable in size to the segments of the polymer molecules.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1958.1202811612
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  • 20
    Electronic Resource
    Electronic Resource
    Kinetics for the tensile strength degradation of nylon and kevlar yarnsPresented as Paper 86-2478 at the AIAA 9th Aerodynamic Deceleration and Balloon Technology Conference, Albuquerque, NM, October 7-9, 1986. (1989)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 37 (1989), S. 2213-2227 
    Details
    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 tensile strength degradation of nylon 66 and Kevlar 29 yarns was studied at elevated temperatures and over a broad range of relative humidities. The degradation rates for nylon are initially slow but increase rapidly, suggesting the depletion of an inhibitor. Kevlar showed no evidence for similar inhibitor action. The effect of relative humidity on degradation can be very large, especially at values in the 90-100% range and at elevated temperatures. Degradation is governed by thermal-oxidative and moisture-induced mechanisms. At the very high humidities and elevated temperatures, the moisture-induced degradation predominates. Rate relationships were developed in which contributions from each mechanism were considered. Calculated degradation from these relationships agrees well with observed degradation over a broad range of temperatures and humidities.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1989.070370813
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