Analyzer system for strippable hydrocarbon on FCC catalyst

Abstract

A FCC process in which spent catalyst is stripped of hydrocarbon in a stripping zone prior to entering the regenerator. In order to maximize the amount of strippable hydrocarbon removed in the stripping zone with minimal use of stripping gas, a sample of spent catalyst is removed prior to entering the regenerator. The spent catalyst is analyzed for strippable hydrocarbon by conducting the sample to a heated catalyst collection vessel, evacuating the catalyst, collecting the gases from the collection vessel and analyzing the gases for amount of strippable hydrocarbon on the spent catalyst.

Description

FIELD OF THE INVENTION

This invention relates to the catalytic cracking of hydrocarbon feeds. More particularly, strippable hydrocarbons from catalyst exiting the stripper are analyzed to enable real time optimization of stripper performance.

BACKGROUND OF THE INVENTION

Fluidized Catalytic Cracking (FCC) is a well known process for converting heavy hydrocarbon feeds to lighter products. Most FCC units include a reactor and a regenerator in the fluid solids portion of the overall FCC process. The movement of catalyst between the reactor and regenerator represents a cyclical process. Heavy hydrocarbon feed is contacted with hot catalyst in the reactor to produce lighter products. During the cracking process, carbonaceous deposits or coke and other contaminants such as metals are deposited on the catalyst resulting in at least a partial deactivation of the catalyst. The deactivated catalyst is separated from the lighter products and sent to a regenerator. The coke deposits are removed from catalyst particles by burning and the regenerated catalyst recycled to the reactor. Heat from coke combustion is typically used to help maintain the desired temperature in the reactor where additional cracking of feed occurs.

Deactivated catalyst particles sent to the regenerator are first subjected to a stripping process to recover a substantial fraction of absorbed hydrocarbon material. The recovered hydrocarbons from the stripping zone are typically added to the cracked hydrocarbons from the FCC reactor to enhance the yield of total hydrocarbon materials. These recovered hydrocarbonaceous materials are then sent for further processing to desired products. The stripped catalyst is sent to a regenerator.

In order to monitor performance of the stripping zone, it is typical to measure coke on catalyst. Current techniques for measuring coke on catalyst do not, however, differentiate between strippable hydrocarbons and non-volatile coke.

It would be desirable to maximize the yield of strippable hydrocarbon from spent FCC catalyst without using excessive stripping gas such as steam. In order to achieve maximum yield with minimal stripping gas, it would be desirable to have a quick and reliable test for measuring strippable hydrocarbon. For example, setting the preferred stripping steam rate for a given feed composition and process conditions is typically a trial and error procedure relating regenerator conditions to steam rate changes.

SUMMARY OF THE INVENTION

The present invention provides a process for treating a hydrocarbon feed in a FCC unit containing a stripping zone whereby strippable hydrocarbon is separately analyzed from non-volatile coke on catalyst. Accordingly, there is provided a catalytic cracking process in which hydrocarbon feed is contacted with zeolite catalyst under catalytic cracking conditions in a reactor zone, catalyst which is at least partially deactivated and cracked hydrocarbon products are separated in at least one separation zone, separated catalyst is at least partially stripped of strippable hydrocarbon in a stripping zone under stripping conditions, stripped catalyst is contacted with oxidizing gas in a regenerator under regenerating conditions to remove carbonaceous deposits from the at least partially deactivated catalyst and regenerated catalyst is contacted with further hydrocarbon feed wherein the improvement comprises:

(a) removing a sample of at least partially deactivated catalyst prior to the regenerator,

(b) conducting the deactivated catalyst sample to a heated catalyst collection vessel;

(c) evacuating the catalyst collection vessel thereby removing strippable hydrocarbon from the deactivated catalyst,

(d) conducting the stripped hydrocarbon to a heated gas collection vessel,

(e) measuring the amount of strippable hydrocarbon in the gas collection vessel, and

(f) conducting the stripped deactivated catalyst sample back to the deactivated catalyst sent to the regenerator..

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a flow diagram showing the process for measuring strippable hydrocarbon from deactivated FCC catalyst.

FIG. 2 is a plot of heat of combustion of coke as a function of hydrogen to carbon ratio of coke burned in the regenerator.

DETAILED DESCRIPTION OF THE INVENTION

The FCC process of this invention provides a method for utilizing analytical information on the amount of strippable hydrocarbon on deactivated catalyst from the FCC reactor to maximize the recovery of such strippable hydrocarbon in the stripping zone with use of minimal stripping gas instead of burning non-recovered hydrocarbon in the regenerator along with coke on catalyst. The present method allows for increased yield of more valuable product streams as compared to using non-recovered strippable hydrocarbon for its fuel value in the regenerator.

A typical FCC reactor includes a reaction zone containing a riser reactor, a separation zone containing one or more cyclones and a stripping zone. In the reaction zone, hot catalyst particles are contacted with fresh feed to form cracked hydrocarbon products and at least partially deactivated (spent) catalyst, i.e., catalyst on which has been deposited coke and/or coke precursors. Separation of cracked hydrocarbon products from spent catalyst occurs in a separation zone containing cyclones. Spent catalyst then passes to a stripping zone. Conventional feedstocks to an FCC unit are gas oils and vacuum gas oils having initial and end boiling points in the range of 204.degree. C. (400.degree. F.) to 566.degree. C. (1050.degree. F.) and Conradson Carbon contents of about 0 to 2 wt. % based on feedstock. Small amounts (5-15%) of higher boiling fractions can be blended into the conventional feedstocks. However, larger amounts of such higher boiling feeds interfere with FCC operation by producing severe coking and even destruction of the catalytic cracking catalyst by the high levels of Conradson Carbon and metals present in the higher boiling feed.

The catalyst which is used in this invention can be any catalyst which is typically used to catalytically "crack" hydrocarbon feeds. It is preferred that the catalytic cracking catalyst comprise a crystalline tetrahedral framework oxide component. This component is used to catalyze the breakdown of primary products from the catalytic cracking reaction into clean products such as naphtha for fuels and olefins for chemical feedstocks. Preferably, the crystalline tetrahedral framework oxide component is selected from the group consisting of zeolites, tectosilicates, tetrahedral aluminophosphates (ALPOs) and tetrahedral silicoaluminophosphates (SAPOs). More preferably, the crystalline framework oxide component is a zeolite.

Zeolites which can be employed in accordance with this invention include both natural and synthetic zeolites. These zeolites include gmelinite, chabazite, dachiardite, clinoptilolite, faujasite, heulandite, analcite, levynite, erionite, sodalite, cancrinite, nepheline, lazurite, scolecite, natrolite, offretite, mesolite, mordenite, brewsterite, and ferrierite. Included among the synthetic zeolites are zeolites X, Y, A, L. ZK-4, ZK-5, B, E, F, H, J, M, Q, T, W, Z, alpha and beta, ZSM-types and omega.

In general, aluminosilicate zeolites are effectively used in this invention. However, the aluminum as well as the silicon component can be substituted for other framework components. For example, the aluminum portion can be replaced by boron, gallium, titanium or trivalent metal compositions which are heavier than aluminum. Germanium can be used to replace the silicon portion.

The catalytic cracking catalyst used in this invention can further comprise an active porous inorganic oxide catalyst framework component and an inert catalyst framework component. Preferably, each component of the catalyst is held together by attachment with an inorganic oxide matrix component.

The active porous inorganic oxide catalyst framework component catalyzes the formation of primary products by cracking hydrocarbon molecules that are too large to fit inside the tetrahedral oxide component. The active porous inorganic oxide catalyst framework component of this invention is preferably a porous inorganic oxide that cracks a relatively large amount of hydrocarbons into lower molecular weight hydrocarbons as compared to an acceptable thermal blank. A low surface area silica (e.g., quartz) is one type of acceptable thermal blank. The extent of cracking can be measured in any of various ASTM tests such as the MAT (microactivity test, ASTM #D3907-8). Compounds such as those disclosed in Greensfelder, B. S., et al., Industrial and Engineering Chemistry, pp. 2573-83, November 1949, are desirable. Alumina, silica-alumina and silica-alumina-zirconia compounds are preferred.

The inert catalyst framework component densities, strengthens and acts as a protective thermal sink. The inert catalyst framework component used in this invention preferably has a cracking activity that is not significantly greater than the acceptable thermal blank. Kaolin and other clays as well as .alpha.-alumina, titania, zirconia, quartz and silica are examples of preferred inert components.

The inorganic oxide matrix component binds the catalyst components together so that the catalyst product is hard enough to survive interparticle and reactor wall collisions. The inorganic oxide matrix can be made from an inorganic oxide sol or gel which is dried to "glue" the catalyst components together. Preferably, the inorganic oxide matrix will be comprised of oxides of silicon and aluminum. It is also preferred that separate alumina phases be incorporated into the inorganic oxide matrix. Species of aluminum oxyhydroxides .gamma.-alumina, boehmite, diaspore, and transitional aluminas such as .alpha.-alumina, .beta.-alumina, .gamma.-alumina, .delta.-alumina, .epsilon.-alumina, .kappa.-alumina, and .rho.-alumina can be employed. Preferably, the alumina species is an aluminum trihydroxide such as gibbsite, bayerite, nordstrandite, or doyelite.

In conducting the catalytic cracking operation, fresh feed and heated catalyst are contacted in a riser. The temperature employed in the riser ranges from about 750.degree. F. (399.degree. C.) to about 1300.degree. F. (1704.degree. C.), preferably from about 900.degree. F. (482.degree. C.) to about 1050.degree. F. (566.degree. C.), and the pressure employed is one ranging from about 0 psig (101 kPa) to about 150 psig (1136 kPa, preferably from about 0 psig (101 kPa) to about 45 psig (411 kPa). Suitably, catalyst/feed ratios in the cracking zone used to convert the feed to lower boiling products are not more than about 30:1 (wt./wt.), and may range from about 20:1 to about 2:1, preferably from about 4:1 to about 9:1. The catalytic cracking process may be carried out in a fixed bed, moving bed, ebullated bed, slurry, transfer line (dispersed phase) or fluidized bed operation, the latter being preferred. More preferably, the catalytic cracking process is carried out in a hydrocarbon/catalyst suspension traversing a tubular reactor or "riser".

Spent catalyst and cracked hydrocarbon products from the riser which is at least partially within a reactor vessel then enters a separation zone within the reactor vessel. Cracked hydrocarbons vapors and catalyst particles pass into at least one cyclone which substanitally separates catalyst from vapor. The deactivated catalyst from the cyclone(s) is conducted to the base of the reactor vessel which functions as a stripping zone.

In the stripping zone, spent catalyst is contacted with steam. Typical stripping steam rates are 2-5 lbs. (0.91-2.3 kg) per 1,000 lbs (454 kg) of circulating catalyst. The steam strips a sizeable fraction (majority) of absorbed hydrocarbons and any emulsion phase hydrocarbons. These hydrocarbons are then combined with cracked hydrocarbon vapor products from cyclones for downstream separation. Inefficient stripping results in undesirable consequences such as loss of product, reduced efficiency of regenerator operations, catalyst deactivation and incomplete regeneration of spent catalyst.

Stripping efficiency is a function of the amount of steam used for stripping. However, increasing the amount of steam must be balanced against the economics of added steam consumption. Typically, stripping efficiency is determined by hydrogen content of coke burned in the regenerator which is in turn determined from an analysis of the amounts of oxygen, carbon monoxide and carbon dioxide in the regenerator flue gas. However, this method cannot discriminate between coke and strippable hydrocarbon (hydrocarbon carryover) remaining on the spent catalyst as it enters the regenerator. FIG. 2 is a plot of heat of combustion of coke as a function of hydrogen to carbon ratio of coke burned in the regenerator.

After the deactivated catalyst is stripped of strippable hydrocarbon, the catalyst is then conducted to a regenerator. Suitable regeneration temperatures include a temperature ranging from about 1100.degree. to about 1500.degree. F. (593.degree. to about 816.degree. C.), and a pressure ranging from about 0 to about 150 psig (101 to about 1136 kPa). The oxidizing agent used to contact the at least partially deactivated (i.e.. coked or spent) catalyst will generally be an oxygen-containing gas such as air, oxygen and mixtures thereof. The at least partially deactivated catalyst is contacted with the oxidizing agent for a time sufficient to remove, by combustion, at least a portion of the carbonaceous deposit and thereby regenerate the catalyst in a conventional manner known in the art.

FIG. 1 shows the stripping zone and analysis zone of this invention. Spent catalyst from cyclone(s) (not shown) is collected as a bed 14 in stripping zone 12 of reactor vessel 11. Steam is admitted to stripping zone 12 through line 15. Stripped hydrocarbon and steam from bed 14 are conducted upwardly through reactor 11 for further separation and processing. Stripped catalyst is conducted from stripping zone 12 to a catalyst regenerator (not shown) through line 16.

Stripped catalyst is removed from line 16 through tap 17. With lower lockhopper valve 22 in the closed position, upper lockhopper valve 21 is opened for a time sufficient to fill the zone 18 between lockhopper valves 21 and 22. Valve 21 is then closed and valve 22 is opened to drop a known volume of catalyst into catalyst collection vessel 23. Vessel 23 is heated by means such as jacket heaters on the shell to promote and maintain volatility of any hydrocarbon remaining on spent catalyst and will typically be at gas pressure less than that in line 16. Valve 22 is closed and valve 24 is opened which allows collection vessel 23 to be evacuated by pump 25. Gases pumped out of vessel 23 are collected in gas collector vessel 26 which is also heated to prevent hydrocarbon condensation. The vacuum pulled on vessel 23 is preferably less than 50 torr. Gas collector 26 will be at pressures of 110 to 310 kPa. Once the desired vacuum on vessel 23 is achieved, valve 24 is closed and valve 27 is opened. This allows gases from gas collector 26 to flow through analyzer 28 and ultimately vented through vent line 31. Valve 29 is then opened to pressurize catalyst collection vessel 23 with inert gas such as steam or nitrogen. Valves 22 and 21 are opened and stripped catalyst is fluidized and blown back into line 16 using gas pressure supplied through valve 29. It is understood that in this step, pressure in vessel 23 is greater than that in line 16.

Analyzer 28 may be any analyzer capable of hydrocarbon analysis under flowing gas conditions, e.g., a gas chromatograph or an infrared spectrometer. Infrared spectrometry is the preferred method of analysis, especially Fourier transform infrared spectrometry. By providing holdup in gas collector 26, the gas flow rate through analyzer 28 need not be metered as the quantity of gas can be calculated knowing the volume, temperature and pressure of gas collector 26. Information from analyzer 28 can be transmitted to steam controller 19 in order that stripping conditions in stripping zone 14 can be optimized for removing the maximum amount of strippable hydrocarbon by adjusting steam addition rate and/or bed height of spent catalyst in stripping zone 14.. This permits the system to operate in on-line mode for continuous operation.

The analyzer system according to the invention is further illustrated by the following example.

EXAMPLE 1

The example illustrates the method for utilizing analytical information on the amount of strippable hydrocarbon on deactivated FCC catalyst to maximize recovery of strippable hydrocarbon. The following table sets forth conditions for stripped catalyst.

TABLE______________________________________ Case I Case II Case III______________________________________Oil Feed, KB/C 85.5 85.5 85.5Riser Outlet Temp., .degree.F. 1020 1018 1020Riser Pressure, psig 33.2 33.2 33.2Cat Oil Raio 5.51 5.51 5.51Regen Bed Temp., .degree.F. 1322 1322 1322Coke on Regenerated Catalyst (wt. %) 0.08 0.08 0.08Coke on Spent Catalyst (wt. %) 0.8 0.8 0.8Flue Gas Composition, Mol %O.sub.2 0.08 0.08 0.08CO.sub.2 17.0 16.9 17.6CO 1.61 1.61 0.6CO.sub.2 /CO Ratio 10.5 10.5 29.8Stripper Temp., .degree.F. 1013 988 990Stripping Stream Klb/hr 25.0 25.0 28.0Coke Make, wt. % on Feed 3.77 3.94 3.77Spent Coke H/C, wt/wt 0.062 0.065 0.062______________________________________

In all three cases, the FCC unit feed is of constant rate and composition. The riser conditions are the same for all of the cases as is the quality of the regenerated catalyst.

In going from Case I to Case II, the stripper temperature has dropped while the stripping steam rate is unchanged at 25.0 klb/hr (11,340 kg/hr). Conventional measures of stripper performance are unchanged. The measured coke on spent catalyst remains at 0.8 wt. %. The composition of the flue gas from the regenerator is also unchanged.

However, the coke make has increased by nearly 5% due to poorer stripping of the adsorbed hydrocarbons on the spent catalyst. Coke is the least economically desirable product from an FCC unit. The hydrogen/carbon ratio on the spent catalyst has increased indicating that the composition of the coke has changed due to the increased strippable hydrocarbon concentration. Conventional monitoring of unit performance would be extremely slow to indicate the increase in coke make; however, the use of this invention would quickly indicate the change in stripper performance thereby allowing real time optimization.

As stripper temperature is not readily controlled, the most likely optimization step is to increase stripping steam rate as shown in case III. By increasing the stripping steam rate by 3.0 klb/hr (1360 kg/hr), the coke make and composition return to the values of the base case, thereby minimizing the product downgrade to coke.

Claims

1. A catalytic cracking process in which hydrocarbon feed is contacted with zeolite catalyst under catalytic cracking conditions in a reactor zone, catalyst which is at least partially deactivated and cracked hydrocarbon products are separated in at least one separation zone, separated catalyst is at least partially stripped of strippable hydrocarbon in a stripping zone under stripping conditions, stripped catalyst is contacted with oxidizing gas in a regenerator under regenerating conditions to remove carbonaceous deposits from the at least partially deactivated and stripped catalyst and regenerated catalyst is contacted with further hydrocarbon feed wherein the improvement comprises:

(a) removing a sample of at least partially deactivated and stripped catalyst between the stripping zone and the regenerator,

(b) conducting the deactivated and stripped catalyst sample to a heated catalyst collection vessel wherein the vessel is heated to a temperature sufficient to promote and maintain volatility of any hydrocarbon remaining on the deactivated and stripped catalyst at a vacuum of 50 torr;

(c) evacuating the heated catalyst collection vessel to less than 50 torr thereby removing remaining strippable hydrocarbon from the deactivated and stripped catalyst,

(d) conducting the remaining stripped hydrocarbon from step (d) to a heated gas collection vessel maintained at pressures of 110 to 310 kPa,

(e) measuring the amount of strippable hydrocarbon in the gas collection vessel,

(f) conducting the stripped deactivated catalyst sample from step (d) back to the deactivated and stripped catalyst sent to the regenerator,

(g) calculating the amount of remaining strippable hydrocarbon present in the sample,

(h) transmitting the calculated information on the value of remaining strippable hydrocarbon present in the sample to a steam controller in the stripping zone, and

(i) adjusting stripping zone conditions to maximize the removal of strippable hydrocarbon in the stripping zone.

2. The process of claim 1 wherein the amount of strippable hydrocarbon is measured with an infrared spectrometer or a gas chromatograph.

3. The process of claim 2 wherein the infrared spectrometer is a Fourier transform infrared spectrometer.

4. The process of claim 1 wherein the stripping zone conditions are maximized for removal of strippable hydrocarbon by adjusting at least one of steam addition rate and bed height of spent catalyst in the stripping zone.

5. The process of claim 1 wherein the calculation of amount of strippable hydrocarbon occurs in on-line mode for continuous operation.