Fluid catalytic cracking based

Catalytic Pyrolysis. This should not be confused with fluid catalytic cracking, which is used in petroleum refining (see Catalysts, regeneration). Catalytic pyrolysis is aimed at producing primarily ethylene. There are many patents and research articles covering the last 20 years (84—89). Catalytic research until 1988 has been summarized (86). Almost all catalysts produce higher amounts of CO and CO2 than normally obtained with conventional pyrolysis. This indicates that the water gas reaction is also very active with these catalysts, and usually this leads to some deterioration of the olefin yield. Significant amounts of coke have been found in these catalysts, and thus there is a further reduction in olefin yield with on-stream time. Most of these catalysts are based on low surface area alumina catalysts (86). A notable exception is the catalyst developed in the former USSR (89). This catalyst primarily contains vanadium as the active material on pumice (89), and is claimed to produce low levels of carbon oxides. 

Nowadays, based on the amount of processed material, hydrotreating is the largest process in heterogeneous catalysis. On the basis of catalysts sold per year, hydro-treating ranks third after automotive exhaust and fluid catalytic cracking [R. Prins, V.H.J. de Beer and G.A. Somorjai, Catal. Rev.-Sci. Eng. 31 (1989) 1]. 

Catalytic cracking is a process that is currently performed exclusively over fluidized catalyst beds. The fluid catalytic cracking (FCC) process was introduced in 1942 and at that time replaced the conventional moving bed processes. These early processes were based on acid-treated clays as acidic catalysts. The replacement of the amorphous aluminosilicate catalysts by Faujasite-type zeolites in the early-1960s is regarded as a major improvement in FCC performance. The new acidic catalysts had a remarkable activity and produced substantially higher yields than the old ones. 

A number of mechanistic modeling studies to explain the fluid catalytic cracking process and to predict the yields of valuable products of the FCC unit have been performed in the past. Weekman and Nace (1970) presented a reaction network model based on the assumption that the catalytic cracking kinetics are second order with respect to the feed concentration and on a three-lump scheme. The first lump corresponds to the entire charge stock above the gasoline boiling range, the second... 

Selective Catalytic Reduction (SCR) has been commercially used since the mid 1980s on fired equipment with the hrst application on a boiler in 1976. The first SCR unit installed on a fluid catalytic cracking unit was at Saibu Oil Company in Yamaguchi, Japan in April 1986. Since then, nearly two dozen ECC units have installed SCR units to remove NO from the flue gas and more are slated to be built in the future. Vendors and catalyst suppliers of this technology include Haldor-Topsoe, Mitsubishi Power Systems, Hitachi, Technip, BASE, and Cormetech. 

Figure 13 The apparent flow regime diagram calculated with EMMS-based multiscale CFD and the intrinsic flow regime diagram for the air-FCC system (fluid catalytic cracking particle, dp = 54 m, pp = 930 kg/m3) calculated by using the EMMS model without CFD. The intrinsic flow regime diagram is independent of the riser height (Wang et al., 2008).

In this section we will present some examples of using the EMMS-based multi-scale CFD to solve industrial problems, including fluid catalytic cracking (FCC) and CFB combustion. 

A model for the riser reactor of commercial fluid catalytic cracking units (FCCU) and pilot plants is developed This model is for real reactors and feedstocks and for commercial FCC catalysts. It is based on hydrodynamic considerations and on the kinetics of cracking and deactivation. The microkinetic model used has five lumps with eight kinetic constants for cracking and two for the catalyst deactivation. These 10 kinetic constants have to be previously determined in laboratory tests for the feedstock-catalyst considered. The model predicts quite well the product distribution at the riser exit. It allows the study of the effect of several operational parameters and of riser revampings. 

Y. Huang, G.V. Reklaitis, and V. Venkatasubramanian. A heuristic extended Kalman filter based estimator for fault identification in a fluid catalytic cracking unit. Industrial Engineering Chemistry Research, 42 3361-3371, 2003. 

The scale-up and design configurations of fluid-bed chemical reactors have evolved rapidly and empirically. An example is fluid catalytic cracking (FCC) [13]. The general fluid-bed concepts developed early. However, the correlations describing the various rate processes and other operational phenomena developed slowly because they could not easily be related back to already established data bases developed for other systems in the case of trickle-bed reactors, data developed for packed-bed absorption towers were utilized. 

The manufacture and use of petroleum-based fuels has been a major factor in the growth and content of chemical engineering. Chemical engineers have pioneered advances in separations, catalytic processes such as fluid catalytic cracking, hydroprocessing, and many others. Many of the advances in chemical engineering science have been stimulated by the need for quantitative understanding of these processes. 

Cerqueira and co-workers203 confirmed the appearance of the of the tetrahedral aluminium and phosphorus in AlPO-like crystalline structures both in beta (BEA) and in MOR zeolites treated with phosphoric acid. 31P MAS,27Al MAS and TQM AS NMR spectra permitted the species present in the samples to be assigned. Possibly, besides the the Altet-f species, other Al species are also taking part in the activity and selectivity of the catalysts. The formation of Alocl o P can also contribute to the increase in the activity by preventing further dealumination. Dual zeolite additives have no impact on the quality of naphtha when compared to MFI-based additives, which are used in the fluid catalytic cracking processes. 

The use of molecular sieve catalysts has also become more widespread in the past decade for the production and inter-conversion of olefins from feedstocks other than oxygenates. The addition of a modified ZSM-5 additive to the Y zeolite-based catalyst can substantially increase the amount of propylene produced in a conventional Fluid Catalytic Cracking (FCC) unit. This has become a very valuable modification, particularly in areas where propylene supplies are tight. More recently, a number of processes have been announced for the direct cracking of C4+ olefinic steams to propylene. These processes also use modified ZSM-5 based... 

The use of CeOs-based materials in catalysis has attracted considerable attention in recent years, particularly in applications like environmental catalysis, where ceria has shown great potential. This book critically reviews the most recent advances in the field, with the focus on both fundamental and applied issues. The first few chapters cover structural and chemical properties of ceria and related materials, i.e. phase stability, reduction behaviour, synthesis, interaction with probe molecules (CO. O2, NO), and metal-support interaction — all presented from the viewpoint of catalytic applications. The use of computational techniques and ceria surfaces and films for model catalytic studies are also reviewed. The second part of the book provides a critical evaluation of the role of ceria in the most important catalytic processes three-way catalysis, catalytic wet oxidation and fluid catalytic cracking. Other topics include oxidation-combustion catalysts, electrocatalysis and the use of cerium catalysts/additives in diesel soot abatement technology. 

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