Riser reaction

In most of today s FCC operations, the desired reactions take place in the riser. In recent years, a number of refiners have modified the FCC unit to eliminate, or severely reduce, post-riser cracking. Quick separation of catalyst from the hydrocarbon vapors at the end of the riser is extremely important in increasing the yield of the desired product. The post-riser reactions produce more gas and coke versus less gasoline and distillate. Presently, there are a number of commercially proven riser disengaging systems offered by the FCC licenser designed to minimize the post-riser cracking of the hydrocarbon vapors. 

An interesting option (Monsanto, Du Pont) involves the use of a riser reaction as shown in Fig. 2.22. The configuration is analogous to a modern FCC unit (see Fig. 2.3). In the riser reactor the (oxidized) catalyst transfers oxygen to the butane substrate giving maleic anhydride. The catalyst is separated from the product in... 

Fresh butane mixed with recycled gas encounters freshly oxidized catalyst at the bottom of the transport-bed reactor and is oxidized to maleic anhydride and CO during its passage up the reactor. Catalyst densities (80 160 kg/m ) in the transport-bed reactor are substantially lower than the catalyst density in a typical fluidized-bed reactor (480 640 kg/m ) (109). The gas flow pattern in the riser is nearly plug flow which avoids the negative effect of backmixing on reaction selectivity. Reduced catalyst is separated from the reaction products by cyclones and is further stripped of products and reactants in a separate stripping vessel. The reduced catalyst is reoxidized in a separate fluidized-bed oxidizer where the exothermic heat of reaction is removed by steam cods. The rate of reoxidation of the VPO catalyst is slower than the rate of oxidation of butane, and consequently residence times are longer in the oxidizer than in the transport-bed reactor. 

Radial density gradients in FCC and other large-diameter pneumatic transfer risers reflect gas—soHd maldistributions and reduce product yields. Cold-flow units are used to measure the transverse catalyst profiles as functions of gas velocity, catalyst flux, and inlet design. Impacts of measured flow distributions have been evaluated using a simple four lump kinetic model and assuming dispersed catalyst clusters where all the reactions are assumed to occur coupled with a continuous gas phase. A 3 wt % conversion advantage is determined for injection feed around the riser circumference as compared with an axial injection design (28). 

The catalytic reactions occur in the vapor phase. Cracking reactions begin as soon as the feed is vaporized. The expanding volume of the vapors that are generated are the main driving force to carry the catalyst up the riser. 

Risers are normally designed for an outlet vapor velocity of 50 ft/sec to 75 ft/sec (15.2 to 22.8 m/sec). The average hydrocarbon residence time is about two seconds (based on outlet conditions). As a consequence of the cracking reactions, a hydrogen-deficient material called coke is deposited on the catalyst, reducing catalyst activity. 

The regenerated catalyst supplies enough energy to heat the feed to the riser outlet temperature, to heat the combustion air to the flue gas temperature, to provide the endothermic heat of reaction, and to compensate for any heat losses to atmosphere. The source of this energy is the burning of coke produced from the reaction. 

In the unit, the heat of reaction is a useful tool. It is an indirect indication of heat balance accuracy. Trending the heat of reaction on a regular basis provides insight into reactions occurring in the riser and the effects of feedstock and catalyst changes. 

Reduction of the catalyst/hydrocarbon time in the riser, coupled with the elimination of post-riser cracking, reduces the saturation of the already produced olefins and allows the refiner to increase the reaction severity. The actions enhance the olefin yields and still operate within the wet gas compressor constraints. Elimination of post-riser residence time (direct connection of the reactor cyclones to the riser) or reducing the temperature in the dilute phase virtually eliminates undesired thermal and nonselective cracking. This reduces dry gas and diolefin yields. 

Riser design. A properly designed riser will help reduce delta coke by reducing the back-mixing of already coked-up catalyst with fresh feed. The back-mixing causes unwanted secondary reactions. 

Post-riser hydrocarbon residence time leads to thermal cracking and non-selective catalytic reactions. These reactions lead to degradation of valuable products, producing dry-gas and coke at the expense of... 

Since the mid-1980s, FCC technology licensors and a number of oil companies have employed a number of RTD s to reduce non-selective post-riser cracking reactions. Two general approaches have been used to reduce post riser cracking. The most widely used approach is direct connection of the cyclones to the riser and on to the reactor vapor line. The second approach is quenching the reactor vapors downstream of the riser-cyclones (rough-cut cyclones). 

Increasing use of riser quench to maximize the reaction mix temperature and to promote maximum vaporization of the feedstiick. 

Riser is a vertical pipe where virtually all FCC reactions take place. 

Figure 7.7b shows the essential features of a refinery catalytic cracker. Large molar mass hydrocarbon molecules are made to crack into smaller hydrocarbon molecules in the presence of a solid catalyst. The liquid hydrocarbon feed is atomized as it enters the catalytic cracking reactor and is mixed with the catalyst particles being carried by a flow of steam or light hydrocarbon gas. The mixture is carried up the riser and the reaction is essentially complete at the top of the riser. However, the reaction is accompanied by the deposition of carbon (coke) on the surface of the catalyst. The catalyst is separated from the gaseous products at the top of the reactor. The gaseous products leave the reactor... 

When a chemical reaction occurs in the system, each of these types of behavior gives rise to a corresponding type of reactor. These range from a fixed-bed reactor (Chapter 21-not a moving-particle reactor), to a fluidized-bed reactor without significant carryover of solid particles, to a fast-fluidized-bed reactor with significant carryover of particles, and ultimately a pneumatic-transport or transport-riser reactor in which solid particles are completely entrained in the rising fluid. The reactors are usually operated commercially with continuous flow of both fluid and solid phases. Kunii and Levenspiel (1991, Chapter 2) illustrate many industrial applications of fluidized beds. 

In the 1970s more-active zeolite catalysts were developed so that the cracking reaction could be conducted in the transport riser. Recently, heavier crude feedstocks have resulted in higher coke production in the cracker. The extra coke causes higher temperatures in the regenerator than are desired. This has resulted in the addition of catalyst cooling to the regeneration step, as shown in Fig. 17-25. 

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