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  • Polymer and Materials Science  (97)
  • Physics
  • 1980-1984
  • 1960-1964  (97)
  • 1963  (97)
Collection
Publisher
Years
  • 1980-1984
  • 1960-1964  (97)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1991-2002 
    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: Infrared spectra indicate that carboxyl-substituted acrylic copolymers react appreci8bly with a butylated melamine-formaldehyde resin when heated at 120°C. for 30 min., but under these conditions acid catalysis is needed before epoxy- or amido-substituted copolymers will crosslink with the melamine-formaldehyde resin. Two methods have been used to synthesize hydroxyl-substituted acrylic copolymers. First, a glycidyl methacrylate copolymer was reacted with diethplamine. Second, an acrylic acid copolymer was heated under reflux with butylene oxide in the presence of a basic catalyst. This second method was used to esterify a vinyl toluene-acrylic acid-acrylamide copolymer which was subsequently treated with paraformaldehyde. The resulting hydroxy-methylolamido copolymer intercondensed when heated at 120°C. for 30 min., somewhat as did the hydroxy copolymer with melamine-formaldehyde resin blends.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 461-468 
    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 changes in solvent resistance and solution viscosity of polyethylene glycol and polypropylene glycol after heating with dicumyl peroxide at 140°C. are consistent with crosslinking of the former and degradation of the latter. Analytical work showed that in both cases all of the peroxide decomposed could be accounted for acetophenone and cumyl alcohol. In the case of polyethylene glycol, crosslinking results from abstraction of secondary hydrogen atoms and dimerization of the resulting radicals; in the case of polypropylene glycol abstraction of tertiary hydrogen atoms leads to radicals which break down by scission at a C—O bond to give a ketone and a more stable radical. This latter process proceeds with an efficiency of unity.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 2467-2476 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of 3-methylbutene-1 by TiCl3-Al(C2H5)3 catalysts in dilute solution above 80°C. yields a polymer which is contaminated with polyethylene. By using tagged aluminum alkyl, this polyethylene was shown to arise almost wholly by displacement of ethylene from the alkyl by the monomer. This side reaction was shown to be a general one in the polymerization of α-olefins other than propylene at elevated temperatures. Analysis of the gas phase above the reaction showed also that some decomposition of the monomer occurs under these conditions.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 125-138 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of N-vinylcarbazole with the TiCl4-Al(i-Bu)3, TiCl4-AlEt3, TiCl3-Al(i-Bu)3, and the TiCl4-n-BuLi systems was studied. It was found that N-vinylcarbazole undergoes a very facile cationic polymerization with TiCl4, or TiCl3, and that catalyst complexes which contain a low metal alkyl/transition metal halide ratio promote a very rapid cationic polymerization. When the catalyst components are mixed in the presence of monomer, considerable cationic polymerization due to the transition metal halide alone takes place before the reaction between the titanium halide and metal alkyl is complete. Experiments with catalyst components mixed in the absence of monomer have shown that the rate of the reaction is markedly dependent on the ratio of the catalyst components and that each system studied had a characteristic ratio at which the catalytic activity suffered a marked drop. With TiCl3-Al(i-Bu)3 this drop occurred at an Al/Ti ratio of 0.8, with TiCl4-Al(i-Bu)3 at an Al/Ti ratio of 3, and with TiCl4-n-BuLi at a Li/Ti ratio of 1.5. This was interpreted as indicating that at these ratios the surface of the titanium halide becomes completely modified by the metal alkyl so that no N-vinylcarbazole-titanium halide interaction could take place. The per cent reduction of TiCl4 to lower valence states was studied with the n-BuLi-TiCl4 system as a function of the Li/Ti ratio and it was found that the maximum per cent reduction takes place at a Li/Ti ratio of 2. The per cent reduction rapidly decreased to zero at higher Li/Ti ratios. The polymers of N-vinylcarbazole formed with Ziegler-type catalyst systems were examined by x-ray diffraction, by their appearance under a polarizing microscope, by infrared spectroscopy, and by nuclear magnetic resonance. These measurements indicated that only amorphous, atactic polymers were formed.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 1 (1963), S. 461-462 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 14 (1963), S. 257-260 
    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: Organic chromates as corrosion inhibitors in primersResearch has been carried out on the corrosion protection afforded by primers based on alkyd resins or zinc chromates with and without inhibitors (organic chromic acid derivates), using as criteria the solubility of the passivating CrO42- ion, the change in the electro-chemical potential, and direct corrosion tests. The best results were obtained with coatings containing 1.8% chromate anion in the form of 1-methylcyclohexanol-1-chromate.
    Notes: Verfolgt wurde der Korrosionsschutzwert von Alkydharz-Grundanstrichen bzw. Grundanstrichen auf Zinkchromatbasis ohne/mit Inhibitoren (organische Derivate der Chromsäure) an Hand des Inlösunggehens des passierenden CrO42--Ions, der Änderung des elektrochemischen Potentials und von direkten Korrosionsversuchen. Beste Ergebnisse zeigten Anstriche, die 1,8% Chromatanion in Form von 1-Methylcyclohexanol-1-Chromat enthalten.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 97-102 
    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: An isotactic polybutene-1 was fractionated, and melting points of several fractions were determined. The fractions were studied by light-scattering and viscosity techniques. The parameters in the Mark-Houwink equation are [η] η 4.73 × 10-5Mw0.80 in heptane at 35°C., [η] = 1.50 × 10-4Mw0.69 in heptane at 60°C., and [η] = 9.49 × 10-5Mw0.73 in decalin at 115°C. The molecular weight range studied was 0.45 × 105 to 0.9 × 106.
    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 7 (1963), S. 545-555 
    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 partial specific volume of wool in water and various organic liquids is determined pyconometrically over the whole range of concentrations during absorption and desorption. Sorption of water in the range 0-2.5% by weight occurs with a constant volume contraction amounting to 36% of the volume of the liquid sorbed. This is due largely to electrostriction of water molecules sorbed on charged groups in the wool. Ethanol sorbed by wool undergoes a rearrangement within the fiber which increases considerably the volume contraction. Volume measurements performed during absorption and desorption indicate reversible behavior with water, n-propanol, isopropanol, and acetone on virgin wool and irreversibility (hysteresis) with n-butanol on virgin wool and with water on supercontracted wool.
    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 7 (1963), S. 451-459 
    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 reactivity ratios in the copolymerizations of N-tert-octyl acrylamide, N-n-octyl acrylamide, and N,N-di-n-butyl acrylamide with styrene and methyl methacrylate have been determined, and the Alfrey-Price Q and e values calculated. The distributed monomer N,N-di-n-butyl acrylamide was found to be more reactive than either N-n-octyl or N-tert-octyl acrylamide, which were of about the same reactivity.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 533-544 
    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: When liquids are sorbed by wool or other textile fibers it is necessary to distinguish between sorbed liquid and liquid held mechanically on the surface and in the interstices between fibers. A method is described by which the latter can be removed by washing the fibers under anhydrous conditions with liquid propane at -78°C. The propane is subsequently distilled off at room temperature leaving the sample of wool containing sorbate. Small corrections are made for loss of sorbate during washing and distillation. The method is accurate to about ±2%. Sorption curves and saturation values are recorded for ethanol, n-propanol, isopropanol, acetone, and n-butanol and initial rates of sorption for n-pentanol, n-hexanol, n-pentane, and benzene. A theory is proposed in which it is postulated that holes of various sizes can be produced by thermal fluctuations and also interactions with the sorbate. A consequence of the theory is that even large molecules can penetrate the fiber if given sufficient time. The experimental values of the initial rate of sorption are interpreted in terms of the volume, shape and ability to form hydrogen bonds of the sorbate molecule. The rate of sorption is very sensitive to quite small modification of the wool fiber. The volume sorption at saturation is found to be constant for water, methanol, ethanol, n-propanol, isopropanol, and n-butanol with a mean value of 34.1 ± 0.7 cm.3/100g.
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