Effect of solvents on the liquid-phase cracking of thermosetting resins

Citation
Y. Sato et al., Effect of solvents on the liquid-phase cracking of thermosetting resins, ENERG FUEL, 13(2), 1999, pp. 364-368
Citations number
6
Categorie Soggetti
Environmental Engineering & Energy
Journal title
ENERGY & FUELS
ISSN journal
08870624 → ACNP
Volume
13
Issue
2
Year of publication
1999
Pages
364 - 368
Database
ISI
SICI code
0887-0624(199903/04)13:2<364:EOSOTL>2.0.ZU;2-U
Abstract
The effect of solvents on the liquid-phase cracking of thermosetting resins was examined in the presence of tetralin (hydrogen-donor solvent), decalin (nondonor solvent), or petroleum heavy oil with a reaction time of 60 min at 430-450 degrees C in a 200-mL autoclave under 2 MPa of initial nitrogen atmosphere. Epoxy and novolak-type phenol resins, as typical thermosetting resins, showed almost 100 wt % conversion and about an 85 wt % yield of dis tillable oil when an iron oxide-sulfur catalyst and tetralin solvent were u sed. With decalin, the oil yield from epoxy resin decreased to 75 wt %; how ever, the phenol resin gave an extremely low conversion of 30 wt % with an oil yield of 25 wt %. Cracking of a resol-type phenol resin gave only 9 wt % conversion with decalin but increased to 99 wt % with tetralin. ABS and u rethane resin also showed high conversions of more than 90 wt % and oil yie lds of 60-90 wt % with tetralin. In all experimental runs, gas yields were very low at 1-3 wt %, except for the case of urethane foam in which about 2 0 wt % of carbon dioxide was produced. In the oil produced from epoxy and p henol resins, 40-74 wt % of phenol compounds were detected. This indicates that liquid-phase cracking proceeds through simple bond dissociation follow ed by quick hydrogen supply from tetralin without any condensation.