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  • Physics  (21)
  • Wiley-Blackwell  (21)
  • International Union of Crystallography (IUCr)
  • 1980-1984  (21)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2817-2834 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal degradation behavior of poly(1,3-phenylene isophthalamide) and poly(chloro-2,4-phenylene isophthalamide) was investigated with the aid of some appropriate model compounds. The pyrolysis products of these materials were identified by gas chromatography (GC), gas chromatography/Fourier transform infrared spectroscopy (GC/FT-IR), and gas chromatography/mass spectrometry (GC/MS). The residual chars were characterized by IR spectroscopy. Thermogravimetric analysis (TGA) was applied to study the effect of end-group concentration on the degradation characteristics of the two polyamides. Kinetic parameters that describe the thermal degradation of the polyamides were also evaluated by TGA. The results of this investigation suggest that the thermal decomposition of these aromatic polyamides involves homolytic as well as hydrolytic cleavages of the amide units.
    Additional Material: 13 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1523-1537 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Detailed understanding of the mechanism of initiation and chain transfer in BCl3-coinitiated isobutylene polymerization led to the efficient synthesis of symmetric telechelic polyisobutylenes carrying ∼CH2C(CH3)2Cl groups at either end of the molecule Cl-PIB-Cl. The synthesis is based on the use of inifers, i.e., bifunctional initiator-transfer agents that effect controlled initiation and propagation in the absence of chain transfer to a monomer. Specifically, the synthesis of Cl-PIB-Cl was achieved by the p-dicumyl chloride/BCl3/isobutylene/CH2Cl2 system. According to the inifer mechanism each Cl-PIB-Cl contains two terminal tertiary chlorines and one phenyl group at the interior of the chains. The structure of this new symmetric telechelic polymer has been established by detailed characterization studies including a sensitive new gel permeation chromatography (UV plus RI) analysis method, 1H-NMR, kinetic experiments, and chemical derivatization. The Cl-PIB-Cl molecule is a key intermediate for the synthesis of hosts of new materials, e.g., triblock copolymers, α,ω-diolefins, and α,ω-difunctional polymers.
    Additional Material: 4 Ill.
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  • 3
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of a new glassy-rubbery-glassy triblock copolymer poly(α-methylstyrene-b-isobutylene-b-α-methylstyrene) has been demonstrated. The key to the synthesis was the preparation by inifer method of a perfectly bifunctional polyisobutylene which carries tert-chlorine end groups Cl-PIB-Cl. In conjunction with Et2AlCl coinitiator, the telechelic Cl-PIB-Cl molecule initiates the polymerization of α-methylstyrene at both ends of the prepolymer. Triblock composition can be controlled by the judicious selection of synthesis conditions; that is, Cl-PIB-Cl molecular weight, α-methylstyrene concentration, and solvent polarity. Theoretical triblock Mn calculated from Mn of Cl-PIB-Cl and triblock overall composition is in excellent agreement with experimental Mn which indicates negligible homopolymer contamination. Extraction with a series of hydrocarbon solvents reveals broad composition distribution. The stress-strain profile of a triblock is similar to that of a poly(styrene-b-butadiene-b-styrene) thermoplastic elastomer of similar composition.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 1875-1884 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The laser-initiated polymerization of charge-transfer monomer complexes was investigated with a pulsed nitrogen laser and an argon laser. Several donor-acceptor monomer charge-transfer systems were screened for polymerization in different solvents. Polymerization by laser initiation was achieved in two of these systems; that is, 2-vinylnaphthalene/fumaronitrile and 9-vinylanthracene/fumaronitrile. The best polymer yields were obtained with the 2-vinylnaphthalene/fumaronitrile system in sulfolane solvent. The influences on the polymer yield and composition of solvents, varying focal path length, glass conditioning, initiation sources, environment, and monomer feed ratios were evaluated. Infrared (IR) spectral studies, gel permeation chromatography (GPC), and chemical analyses were performed to characterize the polymer products arising from the polymerization of 2-vinylnaphthalene/fumaronitrile in sulfolane. The polymer contained a high percentage of sulfolane (ca. 1/3 mol fraction), presumably arising from solvent transfer to the growing polymer chains during the propagation phase of the polymerization.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2103-2119 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The air oxidation of poly-p-xylylene films was studied at temperatures between 125 and 200°C. The oxidation kinetics were obtained from neutron activation (NA) oxygen analyses and infrared (IR) Spectroscopy. A correlation between the NA oxygen analyses and mechanical properties indicated that the amount of oxygen incorporated into these polymers before a significant degradation mechanical properties is about 1000 ppm for poly(dichloro-p-xylylene) and 5000 ppm for poly(monochloro-p-xylylene) or poly-p-xylylene. The activation energy for the oxidation of these polymers was about 30 kcal/mole. Long-term-use (100,000 hr) temperatures were also estimated for each of the poly-p-xylylenes studied. The 100,000-hr maximum continuous-use temperature is 112°C for poly(dichloro-p-xylylene), 72°C for poly(monochloro-p-xylylene), and 57°C for poly-p-xylylene.
    Additional Material: 15 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 3149-3160 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ring-opening, nucleophilic addition of amine-terminated oligomers to alkenyl azlactones was exploited to prepare reactive, that is, in free radical polymerizations, oligomers that could be used in 100% solids resin systems. Acrylamide-functional oligomers resulted from the reaction that used 2-vinyl-4,4-dimethylazlactone, whereas methacrylamide-functional oligomers were produced with 2-isopropenyl-4,4-dimethylazlactone. The overall reaction took place under mild conditions, for example, a few hours at room temperature, and was particularly free of side reactions. Examination of reaction rates with the two alkenyl azlactones revealed that the 2-vinyl derivative reacted ca. four times faster. The (meth)acrylamide-terminated resins were characterized by IR, NMR, and molecular weight analyses.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 1315-1329 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Laser-initiated polymerization of charge transfer monomer complexes has been investigated using an argon ion laser. The influence of solvents, monomer feed ratio, and irradiation time on the copolymer yield and composition was evaluated. The polymer yield was found to be directly proportional to the irradiation time and the molar concentration of maleic anhydride in the monomer feed. An enhanced rate of polymerization was obtained by substituting electron donating groups in the donor monomer. Polymerization, initiation, and propagation mechanisms, via charge transfer complexes, have been discussed. Comparison of laser-induced polymerization with UV-induced polymerization suggests that laser initiation is an energy-efficient process.
    Additional Material: 8 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 813-820 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly-6-(acryloyloxymethyl)uracil was prepared by radical-catalyzed polymerization of monomeric 6-(acryloyloxymethyl)uracil. The reaction of 6-chloromethyluracil with the potassium salt of polyacrylic acids of molecular weights 5000 and 90,000 gave polymers with both carboxylate groups and 50-70% pendant uraciles. Some inferences concerning the arrangement of uracil groups are drawn from the nuclear magnetic resonance (NMR) spectra of the latter polymers. No interaction between poly(A) and the synthetic polymers could be observed.
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1179-1186 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Vinyl-4,4-disubstituted azlactones were shown to be effective comonomers in free radical addition polymerizations for purposes of subsequently preparing radiation-sensitive materials by attaching an unsaturated nucleophile. The azlactone-functional copolymers could be reacted with amine-, thiol-, and hydroxy-functional nucleophiles over the course of a few hours in solution at room temperature to effect covalent attachment of the nucleophile. The electron beam- and UV-sensitive materials were shown to be useful as photoresist and embossable video disk recording media.
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 1573-1585 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The theoretical relations between 13C NMR line intensities and monad, dyad, and triad populations are given. In some cases only approximations are possible. The relations between monads and dyads also between dyads and triads are given. Some necessary relations between line intensities are given which provide a basis for making corrections for differing Overhauser enhancements. Included in the discussion are three lines which have not previously been discussed.
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