Published Date
July 2015, Vol.79:9–13, doi:10.1016/j.renene.2014.07.040
Selected Papers on Renewable Energy: AFORE 2013
Author
Waste particle board
Polypropylene
Catalytic copyrolysis
Bio-oil
H-beta
HY
For further details log on website :
http://www.sciencedirect.com/science/article/pii/S016523701530070X
July 2015, Vol.79:9–13, doi:10.1016/j.renene.2014.07.040
Selected Papers on Renewable Energy: AFORE 2013
Author
Received 17 March 2014. Accepted 22 July 2014. Available online 10 August 2014.
Highlights
- Catalytic co pyrolysis of waste particle board and polypropylene was performed.
- •HY and H-Beta catalysts produced improved bio-oil quality by catalytic copyrolysis.
- •The water content in bio-oil was reduced significantly by copyrolysis with polypropylene.
- •Ga/H-Beta showed high selectivity to the aromatics.
Abstract
The catalytic copyrolysis of waste particle board (WPB) and polypropylene (PP) was investigated for the first time over HY (5.1), HY (30), H-Beta and Ga/H-Beta catalysts. The catalysts were characterized by BET and NH3-TPD analyses. The catalytic pyrolysis of the WPB increased the production of gas products (CO, CO2, C1–C4) compared to non-catalytic pyrolysis. Acids and levoglucosan, which are the main components of bio-oil produced from non-catalytic pyrolysis, were converted to more valuable aromatics, phenolics, and furans through dehydration, deoxygenation and aromatization. The most abundant products from the copyrolysis of WPB and PP were large-molecular-mass hydrocarbons (≥C10). However, catalytic copyrolysis increased the yields of small-molecular-mass hydrocarbons in the gasoline range, aromatics and phenolics. The water content in bio-oil was reduced significantly by copyrolysis with PP, contributing to the improvement in oil quality. HY (5.1) with the largest number of acid sites showed higher catalytic activity than HY (30) and H-Beta because the decomposition and reforming reactions during catalytic copyrolysis occurred on the acid sites of the catalysts. Ga/H-Beta showed even higher selectivity toward the aromatics than H-Beta despite the smaller quantity of acid sites, suggesting that Ga promoted the dehydrocyclization of the reaction intermediates.
Keywords
- ∗ Corresponding author. School of Environmental Engineering, University of Seoul, Seoul 130-743, South Korea. Tel.: +82 2 6490 2780; fax: +82 2 6490 2859.
For further details log on website :
http://www.sciencedirect.com/science/article/pii/S016523701530070X
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