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  • Articles  (379)
  • Polymer and Materials Science  (361)
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  • Physics  (379)
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  • Articles  (379)
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  • Wiley-Blackwell  (379)
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  • 1990-1994  (248)
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  • 1
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Secondary ion mass spectrometry has been used to identify the presence of Cu contamination on undoped semiinsulating GaAs wafer surfaces following polishing under certain conditions. The presence of a contaminating species on the wafer surface is indicated by the influence of pre-etch treatments on electrical measurements performed on heat-treated wafers, with and without Si implants. The identification of Cu as a contaminant is confirmed by photoluminescence measurements. With the appropriate wafer preparation process, the level of Cu contamination is below the SIMS detection limit of 〈1 × 1016 atoms cm-3.In the SIMS analysis of the surface-contaminated wafers, the Cu depth profile shape was dependent on the primary beam bombardment energy, suggesting a chemical segregation of Cu out of the altered layer, a redistribution that is known to occur in Si.To quantify the surface concentration of Cu, GaAs wafers were deliberately contaminated with Cu, heat treated and analysed with glow discharge mass spectrometry and SIMS to provide a cross-calibration.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 221 (1994), S. 187-205 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Polyether auf Triazinbasis können mittels phasentransferkatalysierter Polykondensation bei Raumtemperatur und Reaktionszeiten von 1 bis 3 h hergestellt werden. Von mehr als 20 Polyethern wurden Löslichkeiten, Glasübergangstemperaturen, thermogravimetrische Daten, Reißdehnungen, Reißfestigkeiten, Elastizitätsmoduli und Schlagzähigkeiten bestimmt. Von den Polymeren aus 2,4-Dichlor-6-diethylamino-s-triazin und Bisphenol A wurde zusätzlich der Kristallisationsgrad mittels Röntgenweitwinkelstreuung ermittelt. Das Inkrement des 1,3,5-Triazintriylrings wurde bestimmt, so daß die Glastemperaturen einiger Polyether nach van Krevelen berechnet werden konnten.
    Notes: Triazine-based polyethers can be synthesized by phase transfer catalysed interfacial polycondensation at room temperature and reaction times of about 1 to 3 h. In this way, more than 20 polyethers were synthesized and solubilities, glass transition temperatures, thermogravimetric data, elongations at break, tensil strengths, elasticity moduli and impact strengths were determined. In addition, the degree of crystallinity was investigated for the polymer obtained from of 2,4-dichloro-6-diethylamino-s-triazine and bisphenol A by wide angle X-ray diffraction. The increment of the 1,3,5-triazinetriyl ring was determined, which made it possible to calculate the glass transition temperatures of some polyethers according to van Krevelen.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 1011-1024 
    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 curing reaction of tetraglycidyl diaminodiphenyl methane (TGDDM) with diaminodiphenyl sulfone (DDS) has been investigated using differential scanning calorimetry, Fourier transform IR spectroscopy, and ESR spin trapping techniques. A mechanism has been proposed, and the cure kinetics has been obtained at 177°C. The major conclusion is that cure proceeds mainly through chain extension, while crosslinking occurs through the reaction of hydroxyl groups with epoxides, resulting in formation of ether linkages.
    Additional Material: 11 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 2947-2959 
    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: Blends of high density polyethylene (HDPE) and poly(ethylene terephthalate) (PET) exhibit extremely poor mechanical properties owing to the incompatibility of these two polymers. Such blends, however, would result from the reprocessing of certain carbonated beverage bottles. Addition of small amounts of a commercially available triblock copolymer greatly improved the ductility of these incompatible blends, whereas addition of an ethylene-propylene elastomer did not. The results are discussed in terms of phase morphology and interfacial adhesion among the various components.
    Additional Material: 13 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 3607-3610 
    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: Due to the high chain transfer to monomer, the homopolymerization of methacrylamide yields polymers of extremely low molecular weight. On partial alkaline hydrolysis, the viscosities of these polymers in aqueous solution are much inferior to those of partially hydrolyzed polyacrylamide (HPAM). However, polymethacrylamides prepared by room temperature, persulfate-initiated polymerization in the presence of small amounts of N,N′-methylenebisacrylamide demonstrate posthydrolysis reduced viscosities in 0.01% NaCl comparable to typical commercial HPAM materials.
    Additional Material: 3 Tab.
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  • 6
    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: Five to six million molecular weight polyacrylamide and polymethacrylamides of comparable post-alkaline hydrolysis viscosities were imidized by dissolution and heating in 6N HCl. After alkaline hydrolysis, the imidized polymers demonstrated significantly better retention of viscosity to 2% NaCl than did similar partially hydrolyzed polymers. Viscosities in 0.01% NaCl and resistance to shear were not markedly affected by this modification. It is assumed that this improved performance in brine is the result of chain stiffening due to intrachain imide rings.
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2555-2565 
    ISSN: 0887-6266
    Keywords: in situ molecular composites ; molecular composites ; rigid rod polymer ; molecular modeling ; poly (azomethine) ; epoxy ; glass/epoxy composite ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of rigid rod polymer precursors in a reactive matrix precursor, which is later cured in the mold, constitutes the in situ process. A poly-azomethine (PAM) was used as the rigid rod molecule. The resin used was an epoxy. We discuss the prediction of mechanical properties using micromechanics equations for chopped fiber composites. The chemistry used to synthesize the rigid rod polymer PAM in the epoxy precursor is reviewed. Approaches to better control the cure of these epoxy systems through cure kinetics and cure rheology studies completes the thermoset in situ molecular composite process. There was a 71% increase in tensile modulus in comparison to that of the neat epoxy resin. Molecular modeling simulations and continuum mechanics are used to help understand these findings. PAM/epoxy systems were used as a matrix material in the fabrication of unidirectional glass fiber/(PAM/epoxy) structural composites. © 1994 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 53 (1994), S. 1785-1793 
    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: Di(2-ethylhexyl), di(2-octyl), dihexyl, and dibutyl furan-2,5-dicarboxylate were synthesized from furfural and characterized for their plasticizing abilities toward PVC by dynamic mechanical thermal analysis (DMTA) with di(2-ethylhexyl) phthalate (DOP) as the standard of reference. DMTA gave values for the depression of the glass transition temperature (Tg) per mass fraction of plasticizer, and it also yielded a set of parameters, relative to those for DOP, which describe the compatibility of the furan diesters with PVC. The efficiency in lowering Tg as exhibited by di(2-ethylhexyl) furan-2,5-dicarboxylate is similar to that of its benzenoid analog, DOP, and was determined at 2.41 and 2.45°C per mass % plasticizer, respectively. All four furan diesters were found to be more compatible toward PVC than toward DOP, with dibutyl furan-2,5-dicarboxylate the most highly compatible. © 1994 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 54 (1994), S. 1605-1612 
    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: Additives are commonly formulated into polymers to stabilize them against thermo-oxidative and photo-oxidative degradation. However, the additives themselves undergo degradation in the polymers, especially when the polymers are placed in hostile environments. This study focuses on the degradation of additives in chemical and photo-oxidizing environments; i.e., spas and xenon arc, respectively. HPLC-UV/vis, FT-IR, and GC-MS techniques were utilized to follow the degradation chemistry of the additives. The chemistry was determined for additive degradation by spa chemicals, but the degradation chemistry of benzotriazoles remains elusive due to the insolubility of the resinous degradation products. © 1994 John Wiley & Sons, Inc.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 1137-1147 
    ISSN: 0887-6266
    Keywords: light scattering ; glass transition ; distributions of relaxation times ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Slow relaxing longitudinal density fluctuations in bulk syndiotactic poly (n-butyl methacrylate) [PBMA] were studied by photon correlation spectroscopy as a function of temperature from 70 to 90°C. The shape of the light-scattering relaxation function broadened as the temperature approached the glass transition (Tg = 55°C). The average relaxation time shifted with temperature, consistent with previous studies of PBMA. The relaxation functions were analyzed in terms of a distribution of relaxation rates. The calculated distribution was clearly bimodal and the shape altered with temperature. The higher frequency peak in the distribution corresponds well with previous mechanical and dielectric relaxation studies of the intramolecular relaxation of the acrylate ester side chain. The resolution of the distribution into two modes is due to a well-defined side-chain motion with relaxation strength comparable to the primary glass-rubber relaxation. © 1994 John Wiley & Sons, Inc.
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