Structure and properties of halogenated and nonhalogenated soy-based polyols
✍ Scribed by Andrew Guo; Youngjin Cho; Zoran S. Petrović
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 245 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
✦ Synopsis
Four polyols intended for application in polyurethanes were synthesized by oxirane ring opening in epoxidized soybean oil with hydrochloric acid, hydrobromic acid, methanol, and hydrogen. The structures of the polyols were characterized by spectroscopic, chemical, and physical methods. The brominated polyol had 4.1 hydroxy groups, whereas the other three polyols had slightly lower functionality. The densities, viscosities, viscous-flow activation energies, and molecular weights of the polyols decreased in the following order: brominated Ͼ chlorinated Ͼ methoxylated Ͼ hydrogenated. All the polyols were crystalline solids below their melting temperature, displaying multiple melting peaks. The methoxylated polyol was liquid at room temperature, whereas the other three were waxes.
📜 SIMILAR VOLUMES
Polyurethane (PU) anionomers were prepared as aqueous dispersions using dimethylol propionic acid (DMPA) as the stabilizing moiety. The principal diols used were polytetrahydrofuran of molecular weight 1000 (PTHF1000) and cyclohexane dimethanol (CHDM). The diisocyanates used in this study were isoph
Polyurethane elastomers based on polyols such as polycaprolactone diol of molar mass 2000 and polytetramethylene glycol of molar mass 2000; diisocyanantes such as diphenyl methane 4,4 diisocyanate and dicyclohexyl methane 4,4 diisocyanate; and chain extenders such as bisphenol-A, bisphenol-S, bisphe