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Reactor design and optimization for converting crude (and refinery wastes) to chemicals in one step through steam-fluidized catalytic cracking

Problem statement

The direct catalytic cracking from crude oil to chemicals could dominate the petrochemical industry shortly, with less fuel consumption and increasing production of light olefins and aromatics. We aim to simplify the refinery into a unique one-step conversion scheme, targeting the production of the most demanded petrochemicals.

Using a bottom-up holistic approach, we design a catalytic crude-to-chemicals process toward this goal using a bottom-up holistic approach. We investigate advanced reactors with intrinsic kinetic data and controlled hydrodynamics to improve the process. We study the non-linear multiscale phenomena by coupling the hydrodynamics, heat transfer, and reaction kinetics.

We use particle image/tracking velocimetry experiments, kinetic modeling, computational particle fluid dynamic modeling, and optimization approaches to improve operating scenarios and develop innovative reactor prototypes.

We focus on the catalyst, reactor, and process levels for system enhancement and intensification. We are optimizing several state-of-the-art laboratory and pilot-scale units, including a circulating Berty, downer, and multifunctional fluidized bed reactors.

Goals

  • Develop and scale up advanced reactors for converting crude oil to chemicals through fluid catalytic cracking approaching intrinsic kinetics
  • Model process dynamics using reactive particle fluid dynamics coupled with experimental validations
  • Establish a design workflow for short-contact time reactors based on modeling, prototyping, and testing
  • Analyze the novel process developments in fluid catalytic cracking: novel feedstock, process modifications…
C2C-FCC2023

Related People

Related Publications

Effect of the Catalyst Properties in Polypropylene Pyrolysis Waxes Cracking under FCC Conditions

by Arandes, Torre, Azkoiti, Castaño, Bilbao, De Lasa
Catal. Today Year: 2008

Abstract

The catalytic cracking of polyolefin pyrolysis waxes has been studied under conditions that mimic the operation of a catalytic cracking unit (FCC). Two commercial catalysts of different properties were used. Yields and compositions of the lumps (dry gases, LPG, gasoline and coke) were compared with those corresponding to the actual feed in the refinery (vacuum gas-oil). The effect of process operating conditions (temperature and contact time) is significant. Catalyst acidity has a significant effect on conversion (at a temperature around 525 °C) and on yields and compositions of lumps (in the 500–550 °C range). The main effect of increasing catalyst acidity is an increase in coke content on the catalyst by decreasing the yield to dry gases. Due to the higher hydrogen transfer capacity, the gasoline obtained using the catalyst with higher acidity has a higher aromatic (especially C6–C8) and paraffinic content, and lower olefin content, being these two latter fractions less branched. An increase in catalyst acidity leads to a lower yield of light olefins and to an increase in the yield of paraffins.

Keywords

FCC W2C HCE