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  • 1960-1964  (8)
  • 1945-1949  (1)
  • Chemistry  (9)
Materialart
Erscheinungszeitraum
Jahr
Schlagwörter
  • 1
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 4 (1960), S. 269-276 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The dynamic behavior of elastomers is usually studied in terms of a sinusoidal system. The theoretical and practical limitations of such analysis are discussed. A method which permits calculation of dynamic properties over a wide range of frequencies and forcing functions is described. The theoretical justification and limitations as well as the experimental setup are presented. Using SBR, natural rubber, and butyl, examples of the dynamic responses for various forcing functions are shown. The analogue computer is used to show properties of the above described rubbers which are useful from both the theoretical and application-oriented viewpoints.
    Zusätzliches Material: 23 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 322-330 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: We have found that vulcanizates of MD-551 and butyl rubber at identical crosslink densities have similar properties in low deformation tests at room temperatures. At high extension, the butyl has considerably higher tensile strength which we have associated with crystallization. The MD-551, on the other hand, shows heat stability far superior to that of butyl. It is postulated here that both these differences follow from the nature of the crosslinks in each polymer. The crosslinks in the MD-551 are thought to be both mechanically and chemically more stable than those in butyl. This prevents crystallization on stretching and enhances high temperature stability. Thus far, we have been concerned only with the gum properties of the MD-551. From our previous work, we would expect carbon black to improve the tensile properties of MD-551. Furture work will therefore be concerned with properties of reinforced MD-551. In addition, studies will be made in order to learn more about the crosslinks and how they affect vulcanizate performance.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 62 (1962), S. S145 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 58 (1962), S. 1141-1152 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Sorption of liquids by elastomers is advanced as a means of studying polymer structure. Liquids represent a wider versatility in this regard over vapors since they allow choices of molecular sizes, shapes, and configurational distributions, and thermal effects not available with vapors. Configurations, coiling versus stretched-out molecules, are examined and shown to be of considerable importance in the sorption process. The problem of determination of the concentration dependence is attacked by use of a binary solution as a sorbent or swelling agent. The binary solution is so chosen that one liquid may be considered the solvent and the other liquid a nonsolvent for the particular elastomer. The ternary solution of butyl network - hexane - acetone was used in sorption experiments at 25°C. The total uptake of the binary liquid was measured from zero time to equilibrium in an optical swelling apparatus. Simultaneously, the composition of the binary liquid sorbed at any time was measured in a recording differential refractometer. The two sets of data were combined to calculate the ratio of the two liquids sorbed. The dilution procedure succeeded in varying the apparent activity of the solvent hexane. Preferential sorption of hexane was observed, but significant amounts of the nonsolvent acetone enter the network. The known equilibrium uptake values of hexane from the binary solutions are used to determine the concentration dependence of the diffusion of liquid hexane in a butyl network at 25°C. D0 = 2 × 10-9 cm.2 sec.-1 and a concentration dependence of 10 were obtained by this method. “Activities” for the hexane in the diluted form are calculated for an elastically calibrated network. The activities for the entire concentration range studied agree well with those of a comparable swollen polymer - liquid system such as natural rubber - benzene vapor. Test of the generality of the present method is suggested. Such a test would involve examination of the dependence of the hexane activities so calculated on the nature of the nonsolvent used in the binary liquid.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 29 (1946), S. 1334-1337 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 873-876 
    ISSN: 0449-2986
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 1687-1698 
    ISSN: 0449-2951
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: An examination of the usual terminal and penultimate mechanisms of copolymerization shows that, for a great many comonomer pairs, copolymer composition data are not sufficient to choose one model over the other. The reactivity ratios based on one copolymerization model can be derived from the reactivity ratios of the other model. Predicted copolymer composition, based on both models, will agree with the observed experimental data within the precision of the usual methods used for copolymer analysis. Hypothetical cases and examples from the literature all show this behavior. The literature comonomer systems were α-methylstyrene-acrylonitrile, and styrene with maleic anhydride, citraconic anhydride, and acrylonitrile. Polymer structure, however, predicted by the two mechanisms do differ appreciably in detail. In particular, predictions of the sequential arrangements of the monomers in the copolymers produced are different for the terminal and penultimate mechanisms. It would seem that the development of experimental procedures for determining the sequential arrangement of the comonomers will be necessary before one can easily and definitely distinguish between terminal and penultimate copolymerization models for a particular system.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr 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. 2945-2964 
    ISSN: 0449-2951
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Stereoregular polybutadienes, of both high trans and high cis contents, were isomerized to provide polymers of varying cis-trans content. These isomerizates were used to study structural effects on physical properties. The isomerizations were carried out under photosensitized conditions in benzene solution at 25°C. The reaction was controlled to deliver polymers over the range 0-95% trans content. This range was selected to provide crystalline and semicrystalline polymers whose structures could be examined in terms of sequencing or blocking by established x-ray techniques. Isomer contents were measured accurately by infrared traces. Isomerizations reached an equilibrium of 77% trans regardless of whether the reaction started with high trans or high cis polybutadienes. Intrinsic viscosity was found to increase regularly with trans content in conformity with the larger size of the trans unit. ηsp/c versus c relations were observed to give a complicated form and this subject was deferred for further study. Crystallinity decreased regularly with reduced trans content as the equilibrium of 77% trans was approached. Continued isomerization at the point of equilibrium produced a completely amorphous polymer. The melting temperatures of the crystalline polymers were studied in detail by x-ray camera and counting techniques. These polymers exhibited two crystal forms. One form was stable up to 60°C. and invariant with cis-trans content in the range 80-95% trans. Below 80% trans the melting point of this form decreased with further reduction in trans content. The melting temperature of the other crystal form was dependent on trans content and decreased with decreased trans content until it coincided with the melting temperature of the other form. The distributions of trans and cis units and sequences of them were calculated through construction of matrices of transition probabilities. Copolymer theory was invoked to calculate pseudo reactivity ratios for the trans and cis forms. The melting temperatures of the two crystals were found to follow the predicted curves for random copolymers, although not simultaneously. This behavior is discussed. The crystallinity of the isomerizates of high trans content was found to be similar to block copolymers in spite of the fact that the method of their preparation would require that they be characterized as random. The importance of a crystal transition in this case is stressed along with the general effects due to the amount and type of the noncrystallizable unit.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr 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. 1601-1608 
    ISSN: 0449-2951
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Using normal copolymerization equations we have developed graphical techniques for predicting the amount of crystallinity in ethylene-propylene copolymers.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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