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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 6 (1962), S. 94-97 
    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 proton magnetic resonance in the vitrain of Yūbari caking coal and its residue of pyridine extraction has been studied over the range 90 to 423°K. At lower temperature the absorption line consists of a broad component. At higher temperature this component begins to decrease rapidly in the line width and resolves into two components. This rapid narrowing of the absorption line width suggests a glass transition attributed to the molecular motion in coal. The variation of the second moment of the absorption line with temperature reflects the line width variation. From these results some information on the molecular motion and arrangement in coal have been obtained.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 25 (1972), S. 163-169 
    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: Das Brechungsindexinkrement von acht verschieden zusammengesetzten Terpolymeren aus Styrol, Acrylnitril und Methylmethacrylat wurde in Dimethylfoirmamid und in Butanon bestimmt. Aus der infrarotspektroskopisch ermittelten Zusammensetzung der Copolymeren und den Brechungsinkrementen der Homopolymeren wurden die Brechungsinkremente der Terpolymeren berechnet. Das ptrrtielle azeotrope Terpolymere besitzt ein konstantes Brechungsinkrement während der Terpolymerisation, während die aus anderen Monomermischungen erhaltenen Werte sich mit dem Umsatz ändern.
    Notes: The differential refractive index increment was measured for statistical styrene/acrylonitrile/methyl methacrylate terpolymers of eight different compositions in dimethylformamide and in butanone. With the terpolymer composition obtained from infrared absorption and the differential refractive index increments of the homopolymers, the differential refractive index increments of terpolymers are calculated. The partial azeotropic terpolymer gives a constant value in the course of terpolymerization. The differential refractive index increment of a terpolymer synthesized from other monomer feed than the azeotropic composition changes with conversion.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 82 (1979), S. 55-62 
    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: Die Molekulargewichtsabhängigkeit der Depolarisierung wurde für Polystyrol- und Oligostyrollösungen in Butanon gemessen. Drei wesentliche Ergebnisse wurden erhalten: (1)Die Depolarisationen ϱu der Polystyrol- und Oligostyrollösungen in Butanon zeigen ein Minimum bei einer charakteristischen Konzentration im Gegensatz zu einer Styrollösung in Butanon.(2)Das Depolarisationsminimum fällt mit steigendem Polymerisationsgrad des Oligostyrols und erreicht einen konstanten Wert für Polystyrollösungen von ϱu = 0,0148. In den Oligostyrollösungen stimmt die Depolarisation mit einer theoretischen Berechnung überein, während in Polystyrollösungen eine Beeinflussung durch intra- und intermolekulare Wechselwirkung zu beobachten ist.(3)Die der minimalen Depolarisation zuzuordnende Konzentration C* fällt mit P-½ für Polystyrollösungen und fällt mit P- 1 für Oligostyrollösungen. Dies hängt mit der von einer Gauß-Verteilung abweichenden Verteilung der Oligomersegmente zusammen.
    Notes: The molecular weight dependence of depolarization was measured for polystyrene and styrene oligomer solutions in butanone. Three evident results were obtained: (i)the depolarizations ϱu of polystyrene and styrene oligomer solutions in butanone show a minimum value at a characteristic concentration inspite of that the depolarization of a styrene monomer mixture with butanone shows no minimum value.(ii)the minimum value of depolarization ϱu* decreases with the degree of polymerization, P, for styrene oligomer solutions and reaches a constant value for polystyrene solutions, that is ϱu* = 0.0148. In oligomer solutions the depolarization conforms to the theoretical equation, but in polystyrene solutions the depolarization is affected by both intra-and intermolecular interferences.(iii)the characteristic concentration C*, corresponding to the minimum depolarization ϱu*, decreases with P-1/2 for polystyrene solutions and decreases with P-1 for styrene oligomer solutions. This fact is concerned with the deviation from a Gaussian distribution of oligomer segments.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 48 (1975), S. 175-183 
    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: Eine theoretische Gleichung zur Beschreibung der mittels Lichtsteruung gemessenen Abhängigkeit des scheinbaren Molekulargewichts vom Lösungsmittel wurde im Hinblick auf die Heterogenität der Zusammensetzung abgeleitet. Terpolymere mit einem partiellen Azeotrop wurden aus Styrol, Acrylnitril und Methylmethacrylat hergestellt. Die Molenbrüche betrugen in der angegebenen Reihenfolge 0,55; 0, 16; 0,29. Das mittels Lichtstreuung bestimmte Molekulargewicht erwies sich als vom eingesetzten Lösungsmittel unabhängig. Daraus wurde auf eine homogene Zusammensetzung des Terpolymeren geschlossen. Das Verhältnis zwischen dem Molekulargewicht des Terpolymeren und dem Volumenbruch des Fällungsmittels γ in dem Lösungsmittelgemisch am Fällungspunkt in einem Butanon-Methanol-Terpolymer-System folgte, wie experimentelle Untersuchungen zeigten, der Gleichung worin γ0 und b′ Konstanten bedeuten. Zwischen dem Molekulargewicht und der Viskositatszahl [η] des Terpolymeren gelten die folgenden Beziehungen bei 35°C: und
    Notes: A theoretical equation for the dependence of the apparent molecular weight measured by light scattering on the solvent used has been derived with regard to the composition heterogeneity. Terpolymers corresponding to a partial azeotrope were synthesized from styrene, acrylonitrile, and methyl methacrylate with mole fractions of 0.55, 0.16, and 0.29, respectively. The molecular weight measured by light scattering was found to be independent of the solvent used. Therefore the terpolymer was concluded to be apparently homogeneous in composition. The relationship between the molecular weight M of the terpolymer and the volume fraction of the nonsolvent γ in the solvent mixture at the precipitation point in a butanone-methanol-terpolymer system was experimentally proved to follow the equation where γ0 and b′ are constants. Between the molecular weight and the limiting viscosity number [η] of the terpolymer the following relationships are valid at 35°C: and
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 20 (1956), S. 587-590 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 28 (1958), S. 232-232 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 853-872 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinyl-type monomers containing the pyrrole ring, such as 2-vinylpyrrole (2-VPyrr), N-(pyrrol-2-yl)methylacrylamide (PMA), N-methyl, N-(pyrrol-2-yl)methylacrylamide (MPMA), 2-allylpyrrole (2-AP), β-(pyrrol-1-yl)ethyl vinyl ether (PEVE), 2-diallyl-aminomethylpyrrole (DAMP), and 3-(2-pyrrolylmethyleneimino)propene-1 (PIP) were synthesized by various reactions involving characteristic properties of the pyrrole ring. Radical homopolymerizations and copolymerizations of these monomers were studied. In the homopolymerization of conjugated monomers such as 2-VPyrr and PMA, chain transfer to the pyrrole-containing monomer was remarkable but not degradative. The copolymerization parameters, that is, the values of r1, r2, Q1, and e1 of 2-VPyrr, were determined to be 0.066, 0.69, 5.53, and -1.36, respectively in the copolymerization of 2-VPyrr (M1) with MMA (M2). The Q and e values of the monomers containing a heteroaromatic ring such as 2-vinylpyrrole, 2-vinylfuran, and 2-vinylthiophene were evaluated by the molecular orbital theory. The e value of PMA was found to be negative (-0.64) in the copolymerization with styrene, although e for acrylamide derivatives is generally positive. This may be explained by the intermolecular hydrogen bonding between the carbonyl group and NH group of PMA. That is, attraction or polarization of π-electrons in the vinyl group of PMA is weakened by such hydrogen bonding. From the results of copolymerization of 2-AP with various comonomers, the comonomers could be classified into three categories: class a monomers, in which both Q and e values are largely positive, can copolymerize with 2-AP; class b monomers, having small e values, homopolymerize and can not copolymerize with 2-AP; class c monomers, in which both Q and e values are small. The Q and e values of the comonomer must be largely positive in order to permit copolymerization with an allyl-type monomer.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 1747-1756 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of α-amino acid N-carboxy anhydrides (NCAs) initiated by 4-aminoethylimidazole (histamine) was studied in order to synthesize poly(amino acids) containing an imidazole nucleus at the end of polymer chain. On the basis of the kinetical measurements, it was found that the rate of polymerization is proportional to the first order in both NCA and initiator concentrations and that the initiation reaction is predominantly caused by the primary amine with the highest basicity in a histamine molecule. Binding of the histamine fragment to the end of polymer chain was confirmed by elementary analysis, nuclear magnetic resonance spectroscopy, and measuring the number-average molecular weight of the resulting polymers. It was thus possible to prepare poly(amino acids) with a pendant histamine. In addition, the lowering of the number-average degree of polymerization of the polymers prepared was observed under the condition that the initial molar ratio of NCA to histamine was larger. It was caused by the reinitiation of polymerization by the imidazole nucleus at the chain end.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1243-1255 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The copper complexes and the cobalt complex with the ligand of 3-(2-pyrrolylmethyl-enimino)propene-1 (PIP) or p-(2-pyrrolylmethylenimino)styrene (PIS) were synthesized and homopolymerizations and the copolymerization with styrene, acrylonitrile, methyl methacrylate and acrylic acid studied. In the polymerization of chelate monomers, inhibition of radical polymerization by the central metal ion was observed, but the chelate polymer could be obtained only if the initiator was present in higher concentrations in the feed. It is considered that the strength of inhibition depends on the electronic configuration of d-orbitals of the central metal ion. The initiation mechanism of the cupric chelate monomer may be reduction of the metal ion by the redox reaction with a primary radical via the intramolecular electron transfer through the π-conjugated system of the ligand prior to the propagation step. This mechanism was verified by studying the redox reaction of various copper complexes with DPPH. In the system of the copper complex containing PIS and acylic acid the alternating copolymer could be obtained at any mole fraction of monomer mixture in feed.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 1505-1514 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An interpolymer complex was prepared by mixing aqueous solutions of poly(ethylene oxide) (PEO) and of a poly(carboxylic acid), i.e., poly(acrylic acid)(PAA), poly(methacrylic acid)(PMAA), or styrene-maleic acid copolymer(PSMA). The complexation mechanism was discussed on the basis of results of such experimental methods as viscosity, potentiometric titration, and turbidimetry. The hydrogen bond is primarily involved in these complexations, but the influence of hydrophobic interaction on complexation can not be ignored. If the degree of dissociation α of carboxylic acid or the degree of polymerization Pn of PEO was perceptibly changed, a stable complex was obtained at about α 0.1 or Pn(PEO) = 40 for PMAA, 200 for PAA. This fact indicates that more than a definite number of binding sites are necessary for a stable interpolymer complex to be formed and that cooperative interaction among active sites plays an important role in complex formation.
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