Abstract

Fluidized catalytic cracking (FCC) converts hydrocarbons in the presence of a catalyst based on faujasite zeolite (USY and REY). While hydrocarbon is poorly reactive, biomass and its derived compounds are highly functionalized and not suitable to a typical FCC process. To overcome this limitation biomass was first converted into a dense and stable bio-crude composed mainly of ketal-sugar derivatives by using acetone in diluted acid. Here, a representative compound of this bio-crude, 1,2:3,5-di-O-isopropylidene-α-D-xylofuranose (DX) in n-hexane, was converted by USY and a commercial FCC catalyst containing USY, at 500°C, in a fixed bed and fluidized bed reactors, respectively. Faujasite Y is very efficient in converting DX. More than 95% conversion was observed in all tests. Over 60 wt.% was liquid products, followed by gas products and only around 10% or less in coke. The higher the catalyst activity the greater the aromatics in the liquid products and yet higher coke yields were observed. In particular, simulating more practical application conditions: using deactivated catalyst in a fluidized bed reactor, improved green hydrocarbons production (mono-aromatic up to 10 carbons and light hydrocarbon up to eight carbons) and unprecedented lower coke yield (≈5 wt.%) for bio-feeds. The present results further suggest that catalyst will play a primary role to convert the bio-crude into target hydrocarbons and overcome the transition of a non-renewable to a renewable refinery feed.

Highlights

  • Energy needs have been increasing substantially since the industrial revolution due to population growth and goods demand

  • Catalyst Characterization Used in the Fixed Bed Test

  • The thermal treatment in steam at 500◦C slightly reduced both BET and external area compared to the USY precursor

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Summary

Introduction

Energy needs have been increasing substantially since the industrial revolution due to population growth and goods demand. Natural gas, and coal are the main sources for chemicals, fuel and energy production (Smil, 2004; Conti et al, 2016). Among several alternatives to reduce the carbon footprint, the production of green-fuels for typical refinery process can shorten our transition of a non- to a renewable refinery. As a huge ready-to-use structure for fuel products and distribution is available, and requires simple modifications to the fuel-legislation and no adaptation in motors. Simultaneously this avoids building an entire new structure (Goldthau, 2017). The conversion of biomass into regular fuel using a typical refinery is one of the most important issues that chemistry faces (Ragauskas et al, 2006)

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