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  • Physics  (53)
  • AERODYNAMICS
  • 1970-1974  (87)
  • 1970  (87)
  • 1
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Chloromethylbutadiene has been converted to quaternary ammonium and sulfonium monomers which have been polymerized at room temperature. They show a very great tendency to dimerize on heating in water solution. The aqueous quaternary monomer dimerized 25 times as fast as the aqueous sulfonium monomer and nearly 105 times as fast as neat isoprene at 50°C. The quaternary monomer dimerized with itself in a water solution to which 2-hydroxymethylbutadiene has been added as an example of a nonionic diene. The latter monomer did not dimerize rapidly in water, nor did 2-aminomethylbutadiene. The hydrochlorides of 2-aminomethylbutadiene and 2-dimethylaminomethylbutadiene dimerized at rates comparable to that of the sulfonium monomer. Poly 2-chloromethylbutadiene contains reactive chlorine except for the structure resulting from the minor extent of 1,2 addition. Water-soluble derivatives have been made from it with nucleophilic tertiary amines and sulfides. Cationic polymers are substantive to paper pulp, and the sulfonium polymers can be cured in paper to give improved wet strength.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 2103-2108 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Irradiation of terephthalophenone in isopropyl alcohol gave a bright yellow-colored intermediate which decayed rather rapidly. The products were complex and depended upon the mode of irradiation. They ranged from a mixed polymer I to a dimer II. I consisted of about 5 terephthalophenone units capped with hydrogen or isopropyl alcohol radicals or terminated by cyclization. II, the dimer, was capped by hydrogen atoms.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 2703-2711 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Exposure of poly(ethylene terephthalate) to γ-rays results in the formation of radical I, radical II (tentatively), and to an unassigned radical (III) which is responsible for a central peak in the ESR spectrum. It is believed that completely amorphous samples of polymer contain radicals II and III. On heating, the radicals decay, and the relative proportion of radical III increases. The kinetics of the overall decay process were followed by measuring the decrease in peak height with time. After an initially rapid reaction the decay of the radical population conformed to second order kinetics. An Arrhenius plot of the logarithm of specific rate versus 1/T indicated two lines which intersected at 72°C, which is close to the glass transition temperature. The activation energies were 112 kcal/mole above 72° and roughly 25 kcal/mole below 72°C. Reference to reports in the literature suggests that this decay can be explained by long-range movement of the polymer molecules, even in the glassy solid. The decay of radical I in the crystalline regions of an oriented sample was shown to follow first-order kinetics. As the decay occurs at temperatures as low as 100°C (the melting point is about 260°C), it seems that decay by normal physical movement is unlikely. The results might be explained by invoking the hypothesis of chemical migration of free radical sites by hydrogen atom hopping.
    Additional Material: 6 Ill.
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  • 4
    Publication Date: 2019-07-13
    Description: Stability derivatives for bodies of revolution at subsonic and transonic speeds
    Keywords: AERODYNAMICS
    Type: AIAA PAPER 70-190 , AMERICAN INST. OF AERONAUTICS AND ASTRONAUTICS, AEROSPACE SCIENCES MEETING, 8TH; Jan 19, 1970 - Jan 21, 1970; NEW YORK, NY
    Format: text
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  • 5
    Publication Date: 2019-06-27
    Description: Tables of values of integrals for longitudinal and lateral Von Karman turbulence spectra
    Keywords: AERODYNAMICS
    Type: NASA-TM-X-64529
    Format: application/pdf
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  • 6
    Publication Date: 2019-06-27
    Description: Shock-wave shapes and surface pressures on hemisphere and cone cylinders in low density hypersonic flow including ablation
    Keywords: AERODYNAMICS
    Type: NASA-TN-D-5721 , A-3499
    Format: application/pdf
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  • 7
    Publication Date: 2019-07-13
    Description: Supersonic aerodynamic design tools, discussing technological application of high speed computer and limitations
    Keywords: AERODYNAMICS
    Type: AIAA PAPER 68-1018 , ; TROPHYSICAL JOURNAL|AMERICAN INST. OF AERONAUTICS AND ASTRONAUTICS, ANNUAL MEETING AND TECHNICAL DISPLAY, 5TH; Oct 21, 1968 - Oct 24, 1968; PHILADELPHIA, PA
    Format: text
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 89-103 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The theoretical justification for using M[η], or a similar quantity, as a universal calibration parameter in GPC is reviewed. The equation based on this parameter is applied to transform the primary calibration curve, obtained by means of polystyrene samples, into calibration curves for poly-α-methylstyrene, polypropylene, and linear polyethylene. The Mark-Houwink equations for these polymers, as they are used in the transformation, are discussed. The resulting GPC calibration curves are compared with molecular weights and peak elution volumes of fractionated poly-α-methylstyrene and polypropylene. The same comparison is made with samples of polypropylene and polyethylene having very broad molecular weight distributions. The agreement lies within experimental error.
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 47-59 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A simple method of preparing thin uniform films of high polymers has been examined for growing single crystals from solution. Single crystals of polyethylene, polypropylene, polybutene-1, polyacrylonitrile, and cellulose triacetate have been obtained by this method. Different stages of growth reveal different growth features that are also obtained from solutions of these polymers by changing temperature and concentration.
    Additional Material: 19 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 519-528 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Three transitions are detected dilatometrically when partially isotactic poly(propylene oxide) melts. One transition, the temperature of which is independent of the crystallization temperature over a wide range below 60°C, is ascribed to the melting of lamellar crystallites which are limited in thickness by the average isotactic sequence length alone. The other two transitions, the temperatures of which vary with the crystallization temperature, are ascribed to the melting of lamellar crystallites with thickness determined predominantly by three- and two-dimensional primary nucleation acts. The theory of Flory is adapted and applied quantitatively to the melting points of three crystalline fractions of poly(propylene oxide), obtained from a polymer produced via the zinc diethyl and water catalyst system. This method leads to a thermodynamic melting point of isotactic poly(propylene oxide) near 82°C.
    Additional Material: 3 Ill.
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