Free-Radical Acrylic Polymerization Kinetics at Elevated Temperatures
✍ Scribed by W. Wang; R. A. Hutchinson
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 204 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0930-7516
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Free‐radical acrylic homo‐ and copolymerization kinetics are reviewed, focusing on secondary reactions that impact the polymerization rate and polymer molecular weight (MW) under industrially‐relevant synthesis conditions. Dependent on the monomer type (acrylate, methacrylate, styrene), mechanisms that must be considered include chain‐end depropagation, monomer self‐initiation, formation and reaction of midchain radicals, and incorporation of macromonomers formed by β‐scission of midchain radicals. The relative importance of these reactions varies with temperature and, for copolymerization, monomer composition. A comprehensive treatment of these complexities has been completed for polymerizations conducted up to 180 °C, but further work is required to extend the applicability of the model to even higher temperatures.
📜 SIMILAR VOLUMES
## Abstract Summary: The kinetics of ethene polymerization with metallocene/[Me~2~PhNH]^+^[B(C~6~F~5~)~4~]^−^/Al^__i__^Bu~3~ (ternary systems) and metallocene/methylaluminoxan (MAO) systems respectively has been investigated at 100–140 °C and 7 MPa. Overall, eight different unbridged and __ansa__‐m
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract **Summary:** Living anionic polymerizations are one of the most important methods for the synthesis of well‐defined homo‐ and block copolymers, but these polymerizations are typically carried out at low temperatures, which limits their applications. Deffieux et al. recently reported new