Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 179 (1978), S. 2719-2728 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Results of studies on the determination of the initiation rate of the copolymerization reaction of acrylonitrile with methyl methacrylate, initiated by 2,2′-azoisobutyronitrile in N,N-dimethylformamide at 60°C are reported. The inhibition method used was that involving the stable Banfield's radical (N-[1,1-dimethyl-3-(N-oxidophenyliminio)butyl]-N-phenylaminyl oxide).In the case of acrylonitrile an effect of a side reaction of initiation with the stable radical was observed along with a retarding effect due to inhibition reaction products.In the homopolymerization of methyl methacrylate there takes place a slight effect from a side initiation reaction due to the Banfield's radical, the inhibition reaction products not influencing the further course of the polymerization reaction.The overall contribution of the side initiation reaction changes in the copolymerization of acrylonitrile with methyl methacrylate for different comonomer mixtures with their composition, the actual changes being non-additive. The initiation rate depends on the composition of the monomer mixtures and may be described by the following relation: \documentclass{article}\pagestyle{empty}\begin{document}$ R_i = R_{i,{\rm AN}} \cdot X_{{\rm AN}}^{0,66} + R_{{\rm i,MM}} \cdot X_{{\rm MM}}^{{\rm 1,30}}, $\end{document} where Ri, AN=(8,20±0,15).10-7 mol.dm-3.s-1 and Ri, MM=(7,75±0,25).10-7 mol.dm-3.s-1.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 218 (1994), S. 171-182 
    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 radikalische Polymerisation von Styrol in Substanz mit Azoisobutyronitril als Initiator in Gegenwart des stabilen Radikals 4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl und der zwei Petroleumasphalt-Typen D und F wurde untersucht. Es wurde festgestellt, daß die Petroleumasphalte Substanzen enthalten, welche die Polymerisation inhibieren, aber auch solche, die an Initiierungsreaktionen beteiligt sind. Die Unterschiede im kinetischen Verhalten der Asphalte im Vergleich mit stabilen Radikalen werden diskutiert.
    Notes: A study was made of the free radical polymerization of styrene in bulk at 60°C initiated with 2,2′-azoisobutyronitrile in the presence of the stable free radical 4-hydroxy-2,2,6,6-tetramethyl-piperidine-1-oxyl (TMHPO) and two types of petroleum asphalts D and F. It was found that petroleum asphalts contain compounds effective as polymerization inhibitors and that they also include substances taking part in initiation processes. The differences between the kinetics behaviour of asphalts in comparison with stable free radicals were the subject of the discussion.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Static and dynamic molecular properties are obtained from simultaneous elastic and quasielastic light scattering experiments for nine narrowly distributed polystyrene fractions in nine solvents covering the cross-over region from theta to good-solvent conditions. This set of consistent experimental data is compared with theoretical predictions of two renormalization group theories: the first-order ∊-expansion calculations of Oono et al. and second-order calculations within the “renormalized two-parameter” theory of Douglas and Freed. Static properties (the penetration function) are found to be exactly described by the ∊2-order model, while dynamic behavior seems to be in better accord with Oono's ∊1-order calculations. No evidence of draining effects is detected. Solutions with benzene (and partially with toluene) exhibited atypical, nonuniversal behavior. Some features of static and dynamic exponents behavior in the crossover region are also discussed and compared with previously published theoretical predictions.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 28 (1990), S. 467-479 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This work is the continuation of the investigations of changes in the structure of polystyrene initiated by radiation of wavelengths λ ≥ 270 nm in oxygen-free solutions in CCl4 and CHCl3. Coupled integral and quasielastic light scattering techniques have been applied, enabling observations of changes in the molecular weight distribution function w(M). On the basis of the experimental data and application of Saito and Inokuti's theoretical results, it is shown that in the irradiated solutions polystyrene undergoes simultaneous chain scission and crosslinking. The average number of scissions and crosslinks per macromolecule as a function of irradiation time is calculated. The effect of macromolecular mobility on both photochemical processes is also discussed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 1595-1602 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactivity ratios for various acrylonitrile-phenyl acrylate systems have been determined for radical copolymerization at 60°C in dimethylformamide. The values of the ratios calculated by the linear graphical method of Kelen and Tüdös were as follows: r1 = 0.46 ± 0.02 and r2 = 0.36 ± 0.04 for acrylonitrile-phenyl acrylate, r1 = 0.73 ± 0.02 and r2 = 0.80 ± 0.02 for acrylonitrile-p-cresyl acrylate, r1 = 0.33 ± 0.03 and r2 = 0.9 ± 0.02 for acrylonitrile-p-chlorophenyl acrylate, r1 = 0.82 ± 0.03 and r2 = 1.02 ± 0.03 for acrylonitrile-p-bromophenyl acrylate, r1 = 1.12 ± 0.05 and r2 = 1.16 ± 0.05 for acrylonitryle-o-chlorophenyl acrylate, and r1 = 1.26 ± 0.05 and r2 = 0.86 ± 0.05 for acrylonitrile-m-chlorophenyl acrylate. The dependence of reactivities of the monomers upon their chemical structure was discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1177-1187 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Studies of the initiation rate of the copolymerization reaction of acrylonitrile with p-bromophenyl acrylate initiated by azobisisobutyronitrile in dimethylformamide at 60°C are reported. The inhibition method involved use of stable Banfield's radical (N-[1,1-dimethyl 3-(N-oxidophenylimine)butyl]-N-phenylaminyl oxide). In the case of acrylonitrile, a side reaction effect of the initiation with the stable radical was observed along with a retarding effect resulting from inhibition reaction products (2kdf)60AN = 8.2 × 10-4 min-1. During the inhibited homopolymerization of p-bromophenyl acrylate a very strong side initiation reaction effect results from the Banfield radical; the inhibition reaction products do not influence the further course of the polymerization reaction. Side initiation effects of the Banfield radical (BR) increase with increasing concentration of p-bromophenyl acrylate. The overall contribution of the side initiation reaction changes for different comonomer mixtures; with their compositions the actual changes are nonadditive. The inhibition reaction products do not influence the further course of copolymerization. The initiation rate in monomer mixtures depends on their composition and may be described by the following relation: $$ 2k_d f = (2k_d f)_{{\rm AN}} \times X_{{\rm AN}}^{1.1} + (2k_d f)_{{\rm pBrPhA}} \times X_{{\rm pBrPhA}}^{1.7} $$
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 1 (1980), S. 449-456 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 1 (1980), S. 153-160 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 1 (1980), S. 327-331 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 51-63 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactivity ratios for acrylonitrile - vinyl chloroacetate systems have been determined for radical copolymerization at 60°C in dimethylformamide. The values of the ratios calculated by the linear graphical method of Kelen and Tüdös were as follows: r1 = 4.05 ± 0.1 and r2 = 0.001 ± 0.001 for acrylonitrile (AN) - vinyl monochloroacetate (VCAc), r1 = 7.0 ± 0.25 and r2 = 0.05 ± 0.015 for acrylonitrile - vinyl dichloroacetate (VDAc), r1 = 7.13 ± 0.25 and r2 = 0.06 ± 0.015 for acrylonitrile - vinyl trichloroacetate (VTAc). The penultimate model of the copolymerization and the effect of the vinyl chloroacetate structure were discussed.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...