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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 199 (1992), S. 1-6 
    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: Poly(phenylphosphindiylterephthaloyl), ein neues phosphorhaltiges Polymeres, wurde durch Lösungspolykondensation von Dilithium(phenyl)phosphin mit Terephthaloylchlorid bei niedriger Temperatur hergestellt. Es ist in polaren aprotischen Lösungsmitteln löslich; die inhärente Viskosität in DMF bei 30°C beträgt 19 ml/g. Das Polymere wurde mittels Elementaranalyse sowie IR- und 1H-NMR-Spektroskopie charakterisiert. TGA-Messungen ergeben, daß das Polymere in Luft bis 250°C stabil ist; es ist selbstverlöschend.
    Notes: Poly(phenylphosphinediylterephthaloyl), a novel phosphorus-containing polymer, was synthesized by low-temperature solution polycondensation of dilithio(phenyl)-phosphine with terephthaloyl chloride. The resulting polymer is soluble in polar aprotic solvents, having inherent viscosity of 19 ml/g in DMF at 30°C. The polymer was characterized by elemental analysis, IR and 1H-NMR spectroscopy. TGA data show that the polymer is stable up to 250°C in air. The polymer was found to be self-extinguishing.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 185-200 
    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 sulfur vulcanization of NR by a MBT-TMTD mixed accelerator system both in the presence and absence of ZnO and stearic acid with or without DCP has been studied. The rate of decomposition of DCP in the presence of both MBT and TMTD is quite similar to that in the MBT system alone. The reduction in crosslinking due to DCP is dependent mainly on MBT. The decomposition product of TMTD may contribute to it only at the later stage of vulcanization. Though TMTD has no influence on the decomposition rate, it reacts with MBT at least in the initial stage of vulcanization and suppresses the retardation caused by MBT on DCP vulcanization in accordance with the free sulfur decrease, the nature of crosslinking formation both in the presence and absence of DCP, and the methyl iodide treatment of the vulcanizates. The vulcanization process of the MBT-TMTD-S-NR system has been interpreted in terms of both free radical and polar mechanisms. The domination of either of these depends on the dominant amount of either MBT or TMTD in the acclerator ratio. According to the initial high rate of crosslink formation, free sulfur decrease and also the initial additiveness of crosslinking in stocks containing DCP, the vulcanization process of MBT-TMTD-ZnO-St. acid-S-NR system has been explained in terms of an ionic mechanism. The pronounced synergistic nature of such systems has been interpreted by the enhanced activation of MBT-S-ZnO-St. acid complex due to the dithiodicarbamate ion formed in the initial stages of vulcanization, and also by the activation of TMTD accelerated vulcanization due to the mercaptobenzothiazylion.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    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 Schwefelvukanisation von Naturkautschuk mit der binären beshleunigermischung aus 2-Mercaptobenzthiazol (MBT) und Diphenyiguanidin (DPG) sowohl mit als auch ohne ZnO und Stearinsäure wurde mit und ohne Dicumylperoxid (DCP) eingehend untersucht. Dabei zeigte sich, daß die Zersetzungsgeschwindigkeit von DCP in Gegenwart von MBT und DPG derjenigen bei alleinigem Vorhandensein von MBT ganz ähnlich ist. Die verringerte Vernetzung ist nur von MBT abhängig. Obwohl DPG keinen Einfluß auf die Zersetzungsgeschwindigkeit ausübt, reagiert es mit MBT während der Vulkanisation und unterdrückt die von MBT verursachte Verzögerung. In Übereinstimmung mit der Anfangsadditivität der Vernetzung in DCP enthaltenden Systemen, der freien Schwefelabnahme und der Geschwindigkeit der Vernetzung wurde der Vulkanisierungsprozeß des MBT-DPG-S-NR-Systems durch einen durch MSH2NR′R″ induzierten polaren Mechanismus erklärt. In Gemischen, die DCP zusammen mit Schwefel, MBT, DPG, ZnO und Stearinsäure enthalten, ist das Anfangsstadium der Vernetzung additiv, was durch gemischte Reaktionen und durch Methyljodid-Behandlung der Vulkanisate bestätigt wird. Ein Vergleich rnit einzelnen Beschleunigern zeigt deutlich einen synergistischen Effekt. Dies wird von der gesteigerten Reaktivität des MBT-ZnO-Stearinsäure-Komplexes gegenüber DPG verursacht, das durch die Bildung des aktiven Komplexes MSH2NR′R″ auch eine polare Vulkanisation von Naturkautschuk induziert. Bei Anwesenheit von ZnO und Stearinsäure kann DCP die Vernetzungsdichte nicht vergrößern, es unterdrückt aber die bei seiner Abwesenheit deutliche Vernetzungsabnahme.
    Notes: Sulfuration of natural rubber (NR) by the binary accelerator 2-mercaptobenzothiazole (MBT) and diphenylguanidine (DPG) both in presence and in absence of ZnO and stearic acid with or without dicumylperoxide (DCP) was studied in detail. It was observed that the rate of decomposition of DCP in presence of both MBT and DPG is quite similar to that with MBT alone. The reduction of crosslinking depends also on MBT only. Through DPG has no influence on the decomposition rate, it reacts with MBT during the vulcanization process and suppresses the retardation caused by MBT on the DCP vulcanization. In accordance with the initial additiveness of crosslinking in systems containing DCP, the free sulfur decrease, and the rapidity of crosslink formation the vulcanization process of MBT-DPG-S-NR systems was interpreted in terms of a polar mechanism induced by the complex MSH2NR′R″. In mixtures containing DCP together with sulfur, MBT, DPG, ZnO, and stearic acid, the initial stage of crosslinking is additive as indicated by a mixed reaction as well as by a methyl iodide treatment of the vulcanizates. Comparison with single accelerators shows a pronounced synergistic effect. This is because of the enhanced activity of the MBT-ZnO-stearic acid complex due to DPG which also induces polar sulfuration of NR by forming the active complex MSH2NR′R″. In presence of ZnO and stearic acid, DCP cannot increase the net crosslink density but suppresses the reversion so much pronounced in its absence.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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