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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1295-1307 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ESCA and contact angle measurements were used to characterize the surfaces of Polyethylene and polypropylene films exposed to SF6, CF4, and C2F6 plasmas. None of these gases polymerized in the plasma. However, all plasma treatments grafted fluorinated functionalities directly to the polymer surfaces. SF6 plasmas graft fluorine atoms to a polyolefin surface. CF4 plasmas also react by a mechanism dominated by fluorine atoms, but with some contribution from CFx-radical reactions. Although C2F6 does not polymerize, the mechanism of grafting is still dominated by the reactions of CFx radicals. For all gases studied, the lack of polymerization is attributed to competitive ablation and polymerization reactions occurring under conditions of ion bombardment.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 3343-3348 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ESCA and contact-angle measurements were used to characterize the surfaces of polystyrene films exposed to SF6, CF4, and C2F6 plasmas. SF6 plasmas cause loss of aromaticity in the polystyrene surface region via saturation of the phenyl ring and/or carbon-bond breakage and subsequent fluorination. C2F6 plasmas graft CFx radicals directly to the polystyrene surface without necessarily destroying the aromaticity of the polymer. CF4 plasmas appear to be intermediate in character between SF6 and C2F6 plasmas.
    Additional Material: 1 Ill.
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  • 3
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of complexes between poly(2-vinylpyridine) (P2VPy) and copper chloride was investigated by several techniques, including thermogravimetric analysis and mass spectrometry. P2VPy was selected as the host polymer for two reasons: its ability to form complexes with copper compounds which are soluble in high concentrations, and because it forms essentially no char upon pyrolysis.The decomposition mechanism of P2VPy changes significantly upon complexation with copper compounds. P2VPy was initially thought to be an ideal ligand for the pyrolytic formation of pure copper owing to its low carbon yield upon thermal decomposition. The presence of copper chloride during polymer decomposition alters the decomposition mechanism of the polymer and accounts for significant yields of carbonaceous char. The magnitude of this effect is dependent upon the quantity of copper present. Polymer char yields as high as 41 wt% have been obtained when each pyridine moiety is complexed by CuCl2. Studies based on the model compound Cu(2-picoline)2Cl2 indicate that the diffusion length of released volatiles plays a significant role in the observed decomposition mechanisms.
    Additional Material: 10 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 731-740 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Imidazoles have for some time been recognized as curing agents for epoxy resins. Once the resin and the imidazole compound are mixed there is a relatively short time in which the mixture can be used, since the polymerization (curing) reaction occurs to some extent even at room temperature causing the reaction mixture to thicken. In order to circumvent this problem we have found that imidazoles can be complexed with organo-lanthanide compounds thereby tying up the imidazole and retarding its rate of reaction in the cure of epoxy materials at ambient temperatures. When it is desired to enhance the rate of cure the temperature of the mixture is simply raised. This paper concerns studies of the epoxy cure reaction with the M(THD)3-IM series. M represents the lanthanide metals Eu, Ho, Pr, Dy, Yb, and Gd, and THD is 2,2,6,6-tetramethyl-3,5-heptanedione. Cure reactions were followed by differential scanning calorimetry and in some cases by infrared spectroscopy. We have demonstrated that these organo-lanthanide-imidazole complexes are effective thermally latent curing agents for epoxy resins. At a temperature of 150°C cure is quite rapid. In the course of these studies it has also been determined that there is an inverse correlation between the lanthanide ionic radius in the complex and the temperature at which the cure reaction occurs. Thus the Yb compound, where the imidazole is most strongly bound, cures at the highest temperature and Pr, where imidazole is bound most weakly, at the lowest. Consistent with these facts is the observation that the Yb compound also gives the longest latency period when mixed with epoxy resin.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 16 (1988), S. 191-195 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Protein structure determination of genetically engineered α1-antitrypsin was carried out using the technique of ‘fast atom bombardment (FAB) MAPPING’. CNBr, tryptic and chymotryptic FAB MAPS were produced. The anticipated amino terminal region of the molecule was not mapped at the expected mass, raising the possibility of post-translational modification. A specific experiment was designed to isolate and identify this region by FAB mass spectral screening of high-performance liquid chromatography separated peptides. A signal at m/z 1231 was observed which could not be assigned to any sequence in the molecule using the computer program. Following CNBr treatment, this signal disappeared completely, giving rise to a new signal at m/z 1058. The amino terminus was thus found to be extended by the presence of an N-acetyl methionine residue, and this discovery is the subject of the present paper; another modification within the sequence will be reported elsewhere. Combining the FAB MAPPING data, the overall structural confirmation achieved was 93% of the recombinant α1-antitrypsin molecule.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 56 (1995), S. 1169-1177 
    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 effects of time, temperature, and particulate filler on the tensile behavior of short fiber-reinforced polyphthalamide (PPA) were investigated experimentally. Creep and stress-rupture characteristics and tensile properties before and after isothermal aging were determined. Temperatures ranged from 23 to 150°C and tests lasted up to about 4000 h. Stress-rupture master curves were created, using a WLF-type analysis, which can be used for interpolation with reasonable accuracy. Creep rates were low but were affected by increased moisture absorption in the lowest temperature environment. All properties were affected by chemical degradation of the PPA matrix at the highest temperature. Under most conditions investigated, the mineral filler improved the creep resistance and stiffness of the PPA resin at the expense of strength and ductility. Scanning electron microscopy examinations of fractured specimens indicated that the mineral filler embrittled the matrix and may have damaged the fibers during processing. © 1995 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 10 (1970), S. 1-3 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: An empirical equation is presented which describes polymer solution viscosity, η, over the entire concentration range from a knowledge of intrinsic viscosity, [η], Huggins constant, k′, and bulk flow viscosity of polymer, η0. The equation is: \documentclass{article}\pagestyle{empty}\begin{document}$ \frac{{\eta _{sp}}}{{C[\eta]}} = \exp \left\{{\frac{{{\rm k'[}\eta {\rm]C}}}{{1 - bC}}} \right\} $\end{document} where solution viscosity, η, is contained in ηsp. No arbitrary parameters are invoked since b can be evaluated at bulk polymer (C = polymer density) where everything else is known. The equation accurately portrays the viscosity of polypropylene oxide (PPG 2025) from infinite dilution to bulk polymer in a very good solvent (benzene) and in a somewhat poorer (∼ θ) solvent (methylcyclohexane). The hydrodynamic consequences of the thermodynamic interactions between polymer and solvent are reflected in the constants. This equation should be applicable to other polymer/solvent systems, and thus be immediately useful to those working with concentrated polymer solutions.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 957-957 
    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
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 6 (1972), S. 251-293 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 31 (1991), S. 445-450 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 effects of particle composition and size distribution on the electrical properties of conductive adhesives were studied. Silver-plated glass and silver-plated nickel particles with both narrow (37-44 μm) and broad (〈 44 μm) size distributions were dispersed in an epoxy matrix. In all cases, formulations incorporating narrow particle size distributions required greater concentrations of particles to exceed the percolation threshold for electrical conduction than when broad particle distributions were used. Differences between glass and nickel particles were observed and attributed to the higher density of nickel particles, as well as subtle variations in particle size distributions.
    Additional Material: 9 Ill.
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