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  • 1960-1964  (10)
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Verlag/Herausgeber
Erscheinungszeitraum
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 4 (1964), S. 22-24 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Bicyclo [2.2.1] hepta-2,5-diene, the reaction product of acetylene and cyclopentadiene, and vinyl chloride readily copolymerized by a novel mechanism, to form copolymers containing the nortricyclene group whose softening points rapidly increase with increasing nortricycl one concentration. For each weight per cent copolymerized bicycloheptadiene, the softening point of the vinyl resin is increased about 1°C, making it the most effective comonomer known for this purpose. At the same time increasing nortricyclene concentration disrupts polymer crystallinity, lowers the resin's melting point, and hence its processing temperature, by about 3°C for each weight per cent copolymerized.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 57 (1962), S. 793-799 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Studies of the effect of pressure on comonomer reactivity ratios in the styrene - acrylonitrile and methyl methacrylate - acrylonitrile systems show that the values of r1 and r2 increase in both cases and that the relative activation volumes (ΔV11
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 43 (1960), S. 445-452 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Monomer reactivity ratios have been determined for the copolymerization of methyl methacrylate (M1) and acrylonitrile (M2) catalyzed by alkyl derivatives of lithium, sodium, beryllium, magnesium, boron, aluminum, zinc, and cadmium. Lithium, sodium, beryllium, and magnesium alkyls gave reactivity ratios averaging r1 = 0.34, r2 = 6.7, while alkyls of boron, aluminum, zinc, and cadmium gave r1 = 1.24, r2 = 0.11. These values compare favorably with published reactivity ratios for anionic copolymerization (r1 = 0.25, r2 = 7.9) and free-radical copolymerization (r1 = 1.35, r2 = 0.18). Therefore, alkyl derivatives of groups Ia and IIa metals propagate by an anionic mechanism, while those of groups IIb and IIIa do so by a free-radical mechanism. Confirmatory experiments were run using styrene (M1)-acrylonitrile (M2) solutions. For groups Ia and IIa alkyls the reactivity ratios averaged, r1 = 0.20, r2 = 12.5; and for Groups IIb and IIIa r1 = 0.33, r2 = 0.03. The published values for free-radical catalysts are r1 = 0.41, r2 = 0.04. The formation of free radicals from the groups IIb and IIIa metal alkyls probably arises from oxidation of the metal alkyls by chance traces of oxygen.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 60 (1962), S. S36 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 62 (1962), S. S171 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 67 (1963), S. 219-224 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Eine kürzlich erschienene Theorie von KAWABATA, TSURUTA und FURUKAWA ermöglicht den Vergleich der auf Styrol bezogenen Q-e-Copolymerisationsparameter mit den Konjugationsstabilisierungsenergien, berechnet nach der LCAO-MO-Methode, wobei Äthylen als Bezugsparameter gewählt wurde. Diese Theorie wird an Hand neuerer, auf Äthylen basierender Q-e-Werte nachgeprüft. Während die Übereinstimmung zwischen Theorie und Experiment der auf Äthylen basierenden e-Werte nur mäßig ist und weitere Untersuchungen notwendig macht, werden die auf Äthylen basierenden Q-Werte von der Theorie besser erfaßt. Es werden die Vorteile diskutiert, die bei einem Schema auftreten, das sich nur auf Äthylen als Monomer und Radikal bezieht.
    Notizen: A recent theory by KAWABATA, TSURUTA, and FURUKAWA makes it possible to correlate Q-e values, obtained using styrene as the reference monomer with conjugation stabilization energies calculated from the LCAO-MO method using ethylene as the reference. This theory has been re-examined in light of recently obtained Q-e values based on ethylene. While the agreement between theory and experiment for ethylene-based e values is only fair and indicates the need for further experimentation, quite good agreement is obtained for ethylene-based Q values. The advantages inherent in the use of a scheme based solely on the ethylene monomer and radical are discussed.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 709-713 
    ISSN: 0449-2986
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 2289-2297 
    ISSN: 0449-2951
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: When vinyl chloride - methyl methacrylate copolymers having a uniform chain-to-chain composition, are pyrolyzed at temperatures around 150°C., an intramolecular lactonization occurs forming α-methyl-γ-butyrolactone groups in the polymer backbone concomitant with the quantitative elimination of methyl chloride. This reaction has been shown to be a general reaction for copolymers containing α-substituted γ-haloester groups in their backbone. The formation of the lactone groups in these polymers leads to increased chain rigidity and higher polymer softening points. Advantage has been taken of the gaseous alkyl halide elimination to produce rigid vinyl foams of good compressive strengths.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 1137-1145 
    ISSN: 0449-2951
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Monomer reactivity ratios for the copolymerization of ethylene (M2) with n-butyl acrylate, vinyl chloride, vinyl acetate, and vinyl fluoride have been measured at 1000 atm. The respective values and the experimental temperatures are r1 = 11.9, r2, = 0.03, 70°C.; r1 = 3.6, r2 = 0.24, 90°C.; r1 = 1.08, r2 = 1.07, 90°C.; r1 = 0.16, r2 = 4.39, 160°C. Price Q and e values for ethylene calculated from these reactivity ratios, uncorrected for differences in reaction pressure, are 0.03 and -0.43, respectively. New Q and e values (Q0 and e0) for these four comonomers were calculated on the basis of ethylene rather than styrene as the reference monomer. Assuming that the Q0 and e0 values for ethylene are 1.0 and zero, respectively, the monomer's Q and e0 value are as follows: n-butyl acrylate, 33.3, + 1.02; vinyl chloride, 4.2, + 0.37; vinyl acetate, 0.93, ∼0; vinyl fluoride, 0.25, + 0.6. These Q0 and e0 values give calculated reactivity ratios which are in reasonable agreement with experimental ones. Good agreement is also obtained when the r2 value for the vinyl acetate/ethylene copolymerization is compared with the directly determined rate constant ratio for the addition of an ethyl radical to ethylene and to vinyl acetate, respectively, calculated from previously published data.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 2231-2236 
    ISSN: 0449-2951
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Bicyclo[2.2.1]hepta-2,5-diene, in the presence of free-radical initiators, homopolymerizes to a low molecular weight, soluble polymer containing both 3,5-disubstituted nortricyclene and 5,6-disubstituted bicyclo [2.2.1] hept-2-ene units in the polymer backbone. When the bicycloheptadiene (M2) is copolymerized with vinyl chloride, vinylidene chloride, acrylonitrile, ethyl acrylate, and methyl methacrylate, only the transannular product, 3,5-disubstituted nortricyclene, is found in the high molecular weight copolymers. Reactivity ratios for the above mentioned copolymerizations at 50°C. are: r1 = 0.74, r2 = 0.35; r1 = 1.41, r2 = 0.08; r1 = 0.67, r2 = 0.08; r1 = 3.05, r2 = 0.01; r1 =10.0, r2 = 0; respectively. From these data, the Q and e values for bicyclo[2.2.l]hepta-2,5-diene average 0.09 and -1.04, respectively.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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