Study of curative interactions in cis-1,4-polyisoprene. VI. Interaction of some combinations of sulfur, tetramethylthiuram disulfide, and ZnO
| Autor: | W. J. McGill, F. W. H. Kruger |
|---|---|
| Rok vydání: | 1992 |
| Předmět: |
Exothermic reaction
Polymers and Plastics Vulcanization chemistry.chemical_element Liquefaction General Chemistry Tetramethylthiuram disulfide Photochemistry Sulfur Surfaces Coatings and Films law.invention Differential scanning calorimetry chemistry law Polymer chemistry Materials Chemistry Molecule Curing (chemistry) |
| Zdroj: | Journal of Applied Polymer Science. 44:587-592 |
| ISSN: | 1097-4628 0021-8995 |
| DOI: | 10.1002/app.1992.070440404 |
| Popis: | The interaction of curatives in the systems cis-1,4-polyisoprene (IR)–sulfur, IR–sulfur–ZnO, IR–tetramethylthiuram disulphide (TMTD), and IR–sulfur–TMTD were studied. Thermal events observed in the differential scanning calorimetry curing curves characteristic of these systems were explained in terms of the melting/liquefaction of compounds, the evaporation of gases, and the vulcanization process itself. The similarity of the IR–sulfur and IR–sulfur–ZnO curing curves suggested that sulfur and ZnO were unreactive during vulcanization. On heating the IR–TMTD and IR–sulfur–TMTD systems, gases such as Me2NH and CS2 formed easily. Although the maximum crosslink densities in the latter systems were low, the crosslink formation was found to be strongly exothermic. The sulfur efficiency parameter E was estimated for the IR–sulfur–TMTD system and decreased steeply from 37.5 (at 143.2°C) to 16.6 (at 151.0°C). This was taken as evidence that much of the bound sulfur was initially combined in pendent groups. Then E increased dramatically toward the advanced stages of cure, emphasizing the extraordinary inefficient manner in which sulfur was utilized to form crosslinks. |
| Databáze: | OpenAIRE |
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