The effect of red mud on the liquefaction of waste plastics in heavy vacuum gas oil

Citation
J. Yanik et al., The effect of red mud on the liquefaction of waste plastics in heavy vacuum gas oil, ENERG FUEL, 15(1), 2001, pp. 163-169
Citations number
20
Categorie Soggetti
Environmental Engineering & Energy
Journal title
ENERGY & FUELS
ISSN journal
08870624 → ACNP
Volume
15
Issue
1
Year of publication
2001
Pages
163 - 169
Database
ISI
SICI code
0887-0624(200101/02)15:1<163:TEORMO>2.0.ZU;2-F
Abstract
The main aim of this study was to investigate the effect of red mud on the decomposition and dechlorination of waste plastics. Thermal and catalytic d egradation of a mixture of municipal waste plastics (MWP) and heavy vacuum gas oil (HVGO) into fuel oil was carried out by a onestep and a two-step pr ocess. One-step processing was performed at 430 degreesC by stepwise pyroly sis. Red mud (RM) was used as a dechlorination catalyst. In two-step proces sing, degradation in the presence and absence of solid acid catalyst (silic a-alumina, SA1) was carried out at 430 degreesC followed by dechlorination in a flow-type fixed-bed reactor at 350 degreesC over RM. Copyrolysis of MW P with HVGO led to a synergic effect, increasing the liquid yield. TR99300 had a good dechlorination effect in two-step processing, however it was not effective for MWP/HVGO mixture. In both processes, RM was very effective i n the sorption of both inorganic and organic chlorine compounds. Hydrogen c hloride (HCl) formation from the degradation of poly(vinyl chloride) (PVC) in MWP was depressed by RM. In one-step processing, the yield of liquid pro ducts from the degradation of MWP in HVGO was about 70 wt %. The chlorine c ontent of the liquid product was 1127 ppm in the absence of RM, whereas it decreased to the very low level of 90 ppm in the presence of RM. We obtaine d oil having a negligible amount of chlorine using TR99300 and RM in the tw o-step process. The carbon number distribution of liquid products was simil ar in both processes. The liquid hydrocarbons derived from the degradation of MWP/HVGO were distributed in a wide range of carbon number (C-5-C-25) Wi th a big peak at C-9.