AU640374B2 - Multi-stage wax hydrocracking - Google Patents

Description

OPT DATE 30/1n/91 APPLN. TD 55225 AOJP DATE 05/12/91 P T PCT NUMBER PCT/US90/01893 INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (51) International Patent Classification 5 65/10 (11) International Publication Number: Al (43) International Publication Date: WO 91/15561 17 October 1991 (17.10.91) (21) International Application Number: (22) International Filing Date: PCT/US90/01893 9 April 1990 (09.04.90) FiAL .mEc~zatI lAT I=L L/tLL e.-j.i tit t. t:1rVmtft e Ie n1 T L, 45% 11 IN4 M IM54t i ie. stell tft L -H8c~899Ytff)r I (72) Inventors: NYE, James, R. 107 BalL.ltrae Drive, Elkton, MD 21921 LIPINSKI, John, J. 4 King William Court, Sewell, NJ 08080 SOUDEK, Milos 11919 Briar Forest Drive, Houston, TX 77077 (US).

(74) Agents: HOBBES, Laurence, P. et al.; Mobil Oil Corporation, 3225 Gallows Road, Fairfax, VA 22037 (US).

MU/TiZ oA oR oRCR/AI 3225 ,oe L/ 22 -37 4/ 7 i/el 5/I-/es a/ H4rR/CK (54)Title: MULTI-STAGE WAX HYDROCRACKING (81) Designated States: AT (European patent), AU, BB, BE (European patent), BF (OAPI patent), BG, BJ (OAPI patent), BR, CA, CF (OAPI patent), CG (OAPI patent), CH (European patent), CM (OAPI patent), DE (European patent)*, DK (European patent), ES (European patent), FI, FR (European patent), GA (OAPI patent), GB (European patent), HU, IT (European patent), JP, KP, KR, LK, LU (European patent), MC, MG, ML (OAPI patent), MR (OAPI patent), MW, NL (European patent), NO, RO, SD, SE (European patent), SN (OAPI patent), SU, TD (OAPI patent), TG (OAPI patent).

Published With international search report.

64 0 374 MAKE-UP H 2

VACUUM

GAS OL TO FCC (57) Abstract A process for hydrodewaxing a petroleum or shale oil fraction, petroleum distillate, over a shape selective zeolite in the presence of hydrogen wherein the dewaxing is conducted in at least two stages, (10) and with some of the hydrogen (13) added to first stage effluent Dewaxed feed, and a high octane gasoline byproduct (73) are obtained as products.

See back of page WO 91/15561 PCT/US90/0 1893 -1 MULTI-STAGE WAX HYDROCRACKING The invention relates to wax hydrocracking over shape selective zeolites.

Hydrocarbon conversion processes utilizing crystalline zeolite catalysts have been the subject of extensive investigation during recent years as is clear from both the patent and scientific literature.

Crystalline aluminosilicates have been found to be particularly effective for a wide variety of hydrocarbon conversion processes and have been described and claimed in many patents including U.S. Patent Nos. 3,140,249; 3,140,252; 3,140,251; 3,140,253; and 3,271,418. Aside from serving as general catalysts in hydrocarbon conversion processes, it is also known that the molecular sieve properties of zeolites can be utilized to preferentially convert one molecular species from a mixture of the same with other species.

In a process of this type a zeolite molecular sieve is employed having catalytic activity within its internal pore structure and pore openings such that one component of a feed is capable of entering within the internal pore structure thereof and being converted to the substantial exclusion of another component which, because of its size, is incapable of entering within the pores of the zeolitic material. Shape selective catalytic conversion is also known in the art and is disclosed and claimed in U.S. Patent Nos. 3,140,322; 3,379,640 and 3,395,094.

Although a wide variety of zeolitic materials and particularly crystalline aluminosilicates have been successfully employed in various catalytic conversion processes, nevertheless, these prior art processes, in general, fell into one or two main categories. In one WO 91/15561 PCT/US90!01893 -2 type of conversion process a zeolite was employed which had a pore size sufficiently large to admit the vast majority of components normally found in a charge, i.e., these materials are referred to as large pore size molecular sieves and they are generally stated to have a pore size of from 6 to 13 angstroms and are represented by zeolites X, Y and L. The other type of aluminosilicate was one which had a pore size of approximately 5 angstrom units and it was utilized to preferentially act upon normal paraffins to the substantial exclusion of other molecular species. Thus, by way of considerable over-simplification until recently, there were only two types of aluminosilicates which were available for hydrocarbon processing--those which would admit only normal paraffins and those which would admit all components normally present in a hydrocarbon feed charge. See U.S. Patent No. 3,700,585 and Canadian Patent No. 829,282.

The cracking and/or hydrocracking of petroleum stocks is in general well known and widely practiced. It is known to use various zeolites to catalyze cracking and/or hydrocracking processes.

Of particular recent interest has been the use of a novel class of catalysts to assist in the dewaxing of gas oils, lube base stocks, kerosenes and whole crudes, including syncrudes obtained from shale, tar sands and coal hydrogenation. U.S. Patent No. 3,700,585 discloses the use of ZSM-5 type zeolites to efficiently catalyze dewaxing of various petroleum feedstocks.

U.S. Patent No. 3,700,585 discloses and claims the cracking and hydrocracking of paraffinic materials from various hydrocarbon feedstocks by contacting such feedstock with a ZSM-5 zeolite at about 290' to 712'C., WO 91/15561 PCT/US90/01893 -3 to 200 LHSV and with a hydrogen atmosphere in some cases. This patent is based upon work on the dewaxing of gas oils, particularly virgin gas oils, and crudes although its disclosure and claims are applicable to the dewaxing of any mixture of straight chain, slightly branched chain and other configuration hydrocarbons. The catalyst may have a hydrogenation/dehydrogenation component incorporated therein.

Other U.S. patents teaching dewaxing of various petroleum stocks are U.S. Patent No. Re. 28,398; U.S.

Patent Nos. 3,852,189; 3,891,540; 3,894,933; 3,894,938; 3,894,939; 3,926,782; 3,956,102; 3,968,024; 3,980,550; 4,067,797 and 4,192,734.

Catalytic hydrodewaxing can be considered to be a relatively mild, shape selective cracking or hydrocracking process. It is shape selective because of the inherent constraints of the catalyst pore size upon the molecular configurations which are converted. It is mild because the conversions of gas oil feed to lower boiling range products is limited, usually below percent and more usually below 25 percent. It is operative over a wide temperature range but is usually carried out at relatively low temperatures, e.g. start of run temperatures of 270"C are usual.

An advance in hydrodewaxing was disclosed in U.S.

4,446,007 (Smith). Smith recognized that the dewaxing process could be a source of high octane byproduct gasoline, provided that the temperature was raised relatively rapidly to at least 360'C. Rapid temperature increase after startup meant that there was some over dewaxing of the chargestock, but this was not harmful, and indeed even increased the blending value of the heavy fuel produced. More significantly, the byproduct WO 91/15561 PCr/US90/01893 -4 gasoline was both high octane, and relatively low in aromatic content.

Smith observed that during operation, the mild drop in temperature associated with fresh hydrodewaxing catalyst rapidly diminished, and that hydrogen consumption could be reduced, and reactor delta Ts would approach zero, within a month after startup.

Shape selective catalytic hydrodewaxing such as practiced in U.S. 4,446,007, to produce heavy fuel oil product is not usually considered endothermic or exothermic. Usually reactor temperatures at the outlet roughly equal the inlet temperature. Although the process is a catalytic hydrocracking process, some catalytic hydrodewaxing units create hydrogen rather consume it. They can create H 2 because a long chain paraffin is cracked into two or more olefinic fragments.

This makes H 2 The olefins may or may not be saturated before they leave the hydrocracking reaction zone, and this saturation consumes hydrogen.

To summarize, shape selective catalytic hydrodewaxing to produce fuels is an unusual hydrocracking process in that there is not much temperature change through the reactor, there is not much hydrogen consumption, and it is usually conducted in a single stage. "Single stage" means that dewaxing is customarily conducted in one large reactor, or in several reactors in series, with no intermediate heating, cooling, removal of impurities, etc. between reactor beds. This is in contrast to conventional hydrocracking processes, which usually operate in several stages, with one or more quench stages to prevent temperature runaway.

We realized that catalytic dewaxing unit as proposed in U.S. 4,446,007 (Smith), would give an optimum WO 91/15561 PCT/ US90/01893 startup, but not necessarily an optimum operation thereafter. The rapid start-up procedure of Smith solved the problem of making the dewaxing unit an efficient generator of high octane gasoline during startup, but did not solve the problem of working the catalyst to the maximum extent possible or extending the run length. We discovered a way to make the dewaxing unit produce even more high octane gasoline, and/or last for a longer period of time, than had heretofore been thought possible.

In commercial shape-selective dewaxing units, the process is typically operated in the presence of hydrogen to minimize the amount of coke that is deposited on the catalyst. Dewaxing units typically operate with 360 vol

H

2 /vol feed (2000 SCFB H2), and a hydrogen partial pressure of around 2070-6900 kPa (300-1000 psia), with most operating at a total pressure of 3450 kPa (500 psig) with 2800 kPa (400 psia) H 2 partial pressure.

The hydrogen was believed to be of only minor importance in the wax cracking reactions. The hydrogen was thought to minimize to a great extent the amount of coke laydown that occurs on the catalyst.

Operation with more than 360 vol/vol (2000 SCFB) did not significantly extend catalyst lives as compared to operation with 285-360 vol/vol (1600-2000 SCFB), so this is where most commercial catalytic dewaxing units operate.

At 285 vol/vol feed (1600 SCFB) H 2 addition there is an increased rate of coking, but one which many units can tolerate (with the price of a somewhat shortened catalyst life).

WO 91/15561 PCT/US90/01893 -6 Operation with less than 270 vol/vol feed (1500 SCFB) H 2 230-250 vol/vol feed (1300-1400 SCFB) H2 leads to a rapid increase in coke production.

We analyzed the coke distribution in a commercial dewaxing reactor by observing coke burn during catalyst regeneration. We realized that the coke distribution pattern was highly skewed to the front end of the process. This was consistent with other refiners' experience. In the particular unit studied, the catalyst was split between two reactor vessels, 1/3 of the catalyst being in the first reactor and 2/3 of the catalyst being in the second reactor. Both reactors operated in series, and operated as a single stage.

By operating conventionally, with all of the 1$ hydrogen added being added to the first reactor, and none being added intermediate the first and second reactor, the process operated satisfactorily, but not for as long a period as desired. At the end of the first cycle, the first reactor was heavily coked, while the second reactor had less coke. Decoking the first reactor took 100 hours, while the second reactor, which had twice as much catalyst, was decoked in 30 hours.

The first reactor became coked, and lost activity, requiring a much higher temperature to achieve the specification product pour point. Despite the higher temperature the second reactor was never worked as hard as it could have been (based on its low coke content).

We realized that the shape selective dewaxing catalyst in the second reactor had never been pushed to the maxiumum extent possible, at shut down there was still a very low coke level on the catalyst.

We knew that we could extend the cycle length by minimizing coke formation in the first reactor, by WO 91/15561 PCT/US90/01893 -7 increasing hydrogen partial pressure or increasing hydrogen addition rates above the 285-360 vol/vol feed (1600-2000 SCFB). The drawback to such approach was that increasing the pressure increased the capital expense of the plant, while increasing the hydrogen circulation rates increased both the load on the recycle gas compressor and the duty on the fired, recycle gas heaters. This increased both the capital cost of the plant (for a large compressor and associated piping necessary to circulate the hydrogen) and increased the operating expense (recycle gas compression and heating are two of the largest utility expenses in a dewaxing plant).

We could not afford the capital and operating expenses associated with extending run length by merely increasing the unit pressure or increasing the recycle gas circulation rates. We realized an unconventional approach to hydrogen addition was necessary in order to achieve maximum utilization of the shape selective zeolite dewaxing catalyst, and to minimize the cost of H 2 circulation.

Accordingly, the present invention provides in a process for the shape selective catalytic dewaxing of a wax containing feed comprising at least one of atmospheric gas oil and vacuum gas oil by passing the feed with 180 to 890 vol/vol feed (1000 to 5000 SCFB) of hydrogen over a dewaxing catalyst comprising a shape selective zeolite to produce a dewaxed product and wherein the hydrogen is added to retard catalyst aging, the improvement comprising conducting the dewaxing reaction in at least two stages, with a first stage containing at least 20 wt.% of the dewaxing catalyst and at least 20 wt.% of the dewaxing catalyst being in a WO 91/15561 PCr/US90/01893 -8 stage downstream of the first stage, and adding at least a portion of the hydrogen downstream of the first stage reactor.

Figure 1 is a simplified, schematic view of a dewaxing unit of the present invention.

Figure 2 shows days on stream v. temperature of a commercial dewaxing reactor.

The process of our invention involves many aspects which are conventiorial (such as feedstock, dewaxing catalyst, etc.) and some aspects which are new to shape selective catalytic dewaxing (uneven distribution of H 2 recycle). The conventional aspects will be briefly discussed, followed by a more detailed discussion of the multistage, reheating aspects of our invention.

Any waxy material 'hich has heretofore been processed in shape selective catalytic dewaxing processes can be used. This includes gas oils, lube stocks, kerosenes, whole crudes, synthetic crudes, tar sand oils, shale oils, etc. These heavy feeds may be subjected to one or more conventional pretreatment steps, such as hydrotreating, to remove excessive amounts of nitrogen impurities, metals, etc.

The preferred chargestocks are gas oils and vacuum gas oils derived from paraffinic crudes. Gas oils contemplated for use herein will have boiling ranges of 177-454*C (350 850*F), while vacuum gas oils typically have boiling ranges of 260-482" (500 900'F).

Pour points are at least 24°C e.g., typically 24-38°C (75-100F), or more, frequently, 29-32-C (85-90°F), with cloud points perhaps 2.8'C above the pour point.

The feed preferably is slightly heavier, in terms of end point, than the specification end point of the WO 91/15561 PCT/US90/01893 -9 desired product. This is somewhat heavier than the conventional feed (usually an atmospheric gas oil) to shape selective catalytic dewaxing units making fuel oil products. Some light vacuum gas oil, or material boiling in this range, is preferably present in the feed.

The dewaxing process can convert some feeds boiling beyond the diesel or No. 2 fuel oil boiling range into materials boiling within the desired range. The dewaxing process used herein is not an efficient converter of heavy feeds to lighter feeds, and will leave some fractions of the feed (primarily the aromatic and naphthenic fractions) relatively untouched, so although these non-paraffinic materials can be tolerated in the feed, they are not efficiently converted by the shape selective zeolite catalyst. A relatively heavy feed, with product end point specs satisfied by downstream fractionation, maximizes production of more valuable light products from less valuable heavy feed.

Any conventional shape selective zeolite which can be used to selectively crack normal paraffins in a heavy hydrocarbon stream can be used herein. More details on suitable zeolites, and their properties are disclosed in U.S. 4,446,007.

As disclosed in U.S. 4,446,007, the preferred zeolites have a Constraint Index of 1-12.

Of the zeolite materials useful in the present process, zeolites ZSM-5, ZSM-11, ZSM-12, ZSM-23, ZSM-38 and ZSM-48 are noted. Zeolite ZSM-5 is preferred.

is described in U.S. Pat. No. 3,702,886 and U.S.

Pat. No. Re 29,948. ZSM-11 is described in U.S. Pat.

No. 3,709,979. ZSM-12 is described in U.S. Pat. No.

3,832,449. ZSM-23 is described in U.S. Pat. No.

WO 91/15561 PCT/US90/01893 4,076,842, while U.S. Pat. Nos. 4,016,245 and 4,046,859, describe ZSM-35 and ZSM-38, respectively.

The conditions in each stage of the catalytic dewaxing reaction zone are broadly within those conditions heretofore found suitable for shape selective catalytic hydrodewaxing. More details of preferred conditions are recited in U.S. 4,446,007 (Smith).

Briefly, the shape selective catalytic dewaxing occurs at temperatures from 316-454*C (600-850'F), at LHSVs ranging from 0.1-10. Preferred conditions include temperature of at least 360*C.

Pressures are usually mild, typically on the order of prior art hydrotreating processes ranging around 790-7000 kPa (100-1000 psig). Operation with 2900 kPa (400 pounds) of hydrogen partial pressure gives good results.

In the process of our invention, higher conversions of feed to lighter products are obtained, relative to what was the norm for prior art shape selective catalytic hydrodewaxing processes. Operation at high temperatures suggested in U.S. 4,446,007 (Smith) converts catalytic dewaxing (CDW) from a process which merely dewaxes and produces some low octane gasoline boiling range byproduct, to a process which not only dewaxes but also efficiently generates high octane gasoline which can be added directly to the refinery blending pool. Even more desirably, the high octane gasoline by-product produced by catalytic dewaxing is relatively low in aromatics.

Accordingly, we prefer to operate with somewhat higher temperatures, and conversions than was heretofore considered the norm. Conversions of at least 15 wt.% of the feed to products boiling in the gasoline and lighter range should be achieved, and most preferably conversions WO 91/15561 PCr/US90/893 -11 of 20-45% of the feed to lighter products should be achieved. Depending on paraffin content of the chargestock, conversions of 30-50 wt.% of the feed, or more, to lighter products are contemplated herein.

Gasoline yields of 20-25 wt.% of the feed may be achieved.

Expressed as wt.% conversions of waxy paraffins in the feed, it is preferred to crack most of the paraffins, more preferably, 75 wt.% of the normal and slightly branched paraffins, with 90+% conversions being possible in some cases.

Expressed as gasoline octane, the overall severity should be enough to produce a gasoline boiling range fraction having an octane number (Research Clear) of or higher, preferably above 91, and most preferably above 92.

The average reactor temperature (weight average bed temperature) will preferably be somewhat higher in our process as compared to the prior art, although the average inlet temperature to the first reactor will not change so mucii. This is because we also prefer to operate with higher temperatures in the second stage, by, heating the first stage effluent. Such heating is preferred, but not essential.

The present invention allows the catalytic dewaxing unit to function very efficiently in terms of recycle hydrogen flow. In somewhat oversimplified terms, once we determine that a significant amount of coking has occurred in the upper or upstream portions of the dewaxing reactor, we prefer to then reduce hydrogen circulation to that portion of the reactor. This is the opposite of what might be considered the conventional reaction to cokiig in a reactor, most operators WO 91/15561 PCT/US90/O1893 -12 would attempt to increase the amount of hydrogen added to a reactor which was known to have a coking or loss of activity problem.

By observing the operation of our catalytic dewaxing unit for several years, we realized that the catalyst in the first portion of the CDW bed served to some extent as a guard reactor. In our unit, the CDW catalyst was contained in two reactors, operating in series. The first bed has one third of the catalyst, with the second reactor containing the remaining two thirds. We could easily check the temperature of the stream exiting the first reactor. There was usually a large temperature drop, and this large temperature drop continued even towards the end of a run, when the unit was no longer able to make product with the desired pour point.

We believed that catalyst in the first bed would continue to function as a guard bed and cracker of the easy to crack waxes even when there was quite a lot of coke on the catalyst, and that the unit would continue to function even when the first unit was relatively starved for hydrogen. By shifting some of the recycle gas from the first to the second reactor, we would not have to send all of the recycle hydrogen through all of the catalyst. By sending only a minimal amount of hydrogen through the first reactor, enough to keep the first reactor from becoming a coker, we could send the hydrogen preferentially to the second reactor where it would do more good.

By operating in this way, with the first reactor functioning at a reduced, but stable and relatively rapidly coking mode, and with the second reactor with WO 91/15561 PC/US/01893 -13 maximum hydrogen circulation, it is possible to achieve several improvements.

The energy consumed by the recycle gas coimpressor can be reduced, by recycling more of the H 2 through only the second reactor. This will not improve yields or extend run length, but it will save energy, especially at the end of a dewaxing cycle, with no penalty. The coke level on the first reactor will be significantly higher, and there will be a significant coke level on the catalyst in the second reactor, but decoking requires a complete shutdown of the unit and regenerating with air or an oxygen containing gas, so the incremental cost and inconvenience of burning some more coke from the first reactor is trivial in comparison to the value of the energy saved.

In one embodiment of the invention, hydrogen addition to the first stage is reduced to less than 360 vol/vol feed (2000 SCFB), preferably 130-270 vol/vol feed (750-1500 SCFB), and hydrogen addition to the second stage is increased to 50-270 vol/vol feed (300-1500 SCFB) preferably 90-270 vol/vol feed (500-1500 SCFB), after the first stage catalyst contains at least 5.0 wt. coke.

Run lengths can be conveniently extended by heating the H 2 gas which is preferentially sent to the second reactor. Hot hydrogen is an efficient way of getting some heat into the second reactor, and allowing the dewaxing unit to make on spec product despite loss of activity of catalyst in the first reactor. The extension in run length is believed to be due primarily to the heating effect of the hot H 2 gas added to the second reactor, although there may be some beneficial change in the reaction brought about by starving the first reactor WO 91/15561 PCT/US9/01 893 -14 in H 2 while keeping H 2 rates normal or above normal in the second reactor.

Although it is possible to begin distributed

H

2 recycle from day 1, it is believed to be most beneficial to delay the practice of the invention until near the end of cycle. This will extend the life of the catalyst in the first reactor until it has become coke loaded to a point where further coke loading will not harm it any more.

Where sufficient heater capacity exists, it my be beneficial to begin distributed H 2 processing from the start, shifting more of the dewaxing duty to the second reactor. By operating in this way, with significantly reduced hydrogen and slightly reduced temperatures in the first reactor as compared to prior art methods of operating dewaxing reactors, it may be possible to extend even further the cycle lengths achievable in shape selective catalytic dewaxing processes, and/or increase throughputs and/or conversion.

Some of the benefits of distributed hydrogen recycle should be seen when as little as 10 to 20% of the recycle H2 stream is added to the reactor downstream of the first reactor inlet. When the process is operated with 285-360 vil/vol feed (1600-2000 SCFB) H 2 recycle gas to the first reactor (in a two reactor system) 50-270 vol/vol feed (300-1500 SCFB), and preferably 142-214 vol/vol feed (800-1200 SCFB), additional H2 may be added to the second reactor. Preferably 10-50% or more of the total amount of recycle H2 is added only to the second reactor. In one embodiment, the fresh or make-up hydrogen may be added to the first reactor with the fresh feed, while the recycle hydrogen is added only to the second reactor.

WO 91/15561 PC~/US90/01893 Another preferred embodiment involves adding the make-up H 2 only to the second reactor and recycling H 2 only to the first reactor. This will be preferred whenever a relatively low pressure source of H2 is available, such as a Pt reformer. By heating the makeup

H

2 and adding it at a relatively low pressure point (downstream of the first reactor) the capacity of the CDW unit can be increased.

It would be possible to conduct the process in 3, 4, or even more reactor-, but in most instances the benefits to be gained by such an elaborate reactor design will not be offset by the cost associated with the elaborate design.

When a two reactor system is used, the first reactor should contain 25-70% of the total inventory of shape selective zeolite catalysts, while the second reactor should contain 30-75%.

Based on our experimental work with one commercial unit (with about a 1/3-2/3 split between catalyst in the first and second reactors) we believe that in future installations the optimum catalyst loading will be about the same.

For a three reactor system, the first reactor could contain 10-40% of the total catalyst inventory, while the second reactor could contain 20-40%, with the remainder being in the third reactor.

Heat can also be added in many ways to the second reactor. The easiest method for a retrofit is addition of a hot hydrogen stream. Any other conventional means of getting heat into the second stage can be used, e.g., indirect heat exchange, addition of some hot material which is not harmful to the process, or passing the first WO 91/15561 PC/US90/01893 -16 reactor effluent through a fired heater. Such heating of downstream stages is beneficial, but not essential.

The present invention can be better understood with reference to the attached figures. Figure 1 shows a considerably simplified process flow diagram of cne embodiment of the invention, while Figure 2 shows average reactor temperatures versus days on stream during several commercial tests of a dewaxing unit.

In Figure 1, a combined heavy feed, comprising a Heavy Atmospheric Gas Oil (HAGO), Light Vacuum Gas Oil (LVGO) and FCC Intermediate Cycle Oil (ICO) are added via line 4, mixed with makeup H2 rich gas in line 2, and passed through heat exchanger 20 and line 5 into heater 6. The heated feed is charged via line 8 into the first stage reactor 10. The first stage effluent is removed via line 12. The first reactor effluent, within a month after startup, usually is at least 10°C cooler than the feed in line 8. There is a drop in temperature because of the endothermic wax cracking reactions occurring in first stage reactor 10. First stage effluent is heated, by adding hot hydrogen from line 13. The resulting mixture is passed into second stage reactor 15. The dewaxed heavy feed, cracked products and H2 are removed via line 19, passed through heat exchanger 20 and discharged via line 21 into high pressure separator Actually, the figure is quite a simplification of the actual refinery operation. All of the feed, and much of the recycle H2 was charged to a heater and then passed to reactor i. The heater 6 could not handle the load, so we used a separate heater 16, which happened to be available. This second heater was used to heat a portion of the recycle gas and makeup H 2 The material from both heaters entered the first reactor. The first reactor WO 91/15561 PCT/US90/01893 -17 functioned just as it would have with a conventional single heater for the combined stream of oil and recycle and makeup gas. Our unusual heater system (with two heaters instead of the more normal single heater) was then further modified, by the addition of a line equivalent to line 13 shown in Figure 1, to allow us to add hot recycle H 2 directly to the reactor 1 effluent, and thereby heat the feed to the second reactor.

Our actual point of H 2 addition was also somewhat different than that shown in Figure 1, but the difference is not important to the process. The makeup H 2 purity from a Pt reformer varies from day to day because of normal fluctuations of the reformer. The shape selective catalytic dewaxing unit usually cleans up the hydrogen, which is a little unusual for a hydrogen consuming unit.

Thus there is very little difference in hydrogen purity of the makeup H 2 to the dewaxing unit and the H 2 purity of the dewaxing unit recycle gas, so the point of addition of makeup H 2 is not critical. In our plant, the makeup H 2 was added to the recycle H 2 Some of the combined H 2 stream (recycle makeup H 2 was mixed with the oil feed, and the remainder of the combined H 2 was sent to the second heater, to the heater with no oil feed.

High pressure separator 25 operates at a temperature of 16-540C (60-130'F) and pressure of 3700 kPa (525 psig). A hydrogen rich gas stream is withdrawn via line 24 and removed as a fuel gas by-product in line 71, recycled to mix with fresh feed via line 22 or sent via line 23 to heater 16 to produce; the hot hydrogen rich gas in line 13.

Liquid is removed from high pressure separator via line 28 and discharged into low pressure separator WO 91/15561 PCT/US90/01893 -18 operating at a temperature of 16-54°C (60-130"F) and a pressure of 1310-1340 kPa (175-180 psig). A fuel gas stream is removed via line 29. Flashed liquid is removed via line 31 and charged to stabilizer or debutanizer

C

4 and lighter hydrocarbons are removed overhead via line 39, cooled in cooling means not shown, and charged to overhead accumulator 40. The figure is also somewhat simplified re this and other distillation columns, i.e., reflux line, coolers associated with column overhead vapor lines, pumps, etc. have been omitted for clarity.

A fuel gas stream is removed via line 41 while a C3/C 4 rich liquid is discharged via line 72, for further processing in the FCC depropanizer.

Stabilizer 35 is reboiled using conventional reboiler 36. The net bottoms products is removed via line 37, passed through heater 46 and discharged via line 44 into splitter column 45. Gasoline boiling range hydrocarbons are removed overhead via line 47 and discharged into overhead accumulator 55. Gasoline boiling range hydrocarbons are removed via line 73 as a product.

An intermediate boiling range stream is removed from column 45 via line 49 and charged to steam side stripper 50. Light materials are discharged overhead via line 52 and sent back to the main column 45, while a diesel fraction is removed via line 74 as a product.

A bottoms product is withdrawn via line 59 from column 45 and charged to vacuum flash 60. An overhead vapor stream is removed via line 63 and charged to overhead accumulator 55 for recovery of gasoline boiling range components. An intermediate boiling range stream is withdrawn via line 62 and charged to steam side WO 91/15561 PCr/US90/01893 -19 stripper 50, while a vacuum gas oil fraction is withdrawn via line

EXAMPLE

The invention was tested in a commercial dewaxing unit. As is common in all operating commercial units, the unit was being run to make a product, not to generate data. There are always changes in operation, and problems so there is quite a scatter in the data generated by a commercial plant. The commercial test occurred at a refinery which runs heavy paraffinic crudes, with attendant distillate fluidity problems.

The refinery chose shape selective catalytic dewaxing as the most cost effective way of eliminating distillate cold flow problems and improving plant profitability. The refinery had an idle high pressure hydrotreating unit which was built in 1972 to pretreat 2700 m 3 per stream day (17,000 BPSD) of heavy FCC naphtha prior to reforming. For a number of reasons, the unit was mothballed. This unit contained most of the equipment required by the CDW process except for the addition of one major vessel. Changes were made to the piping and reactor internals and the unit pressure was dropped to 3700 kPa (525 psig). Figure 1 is a schematic of the revamped unit.

WO 91/15561 PCT/US90/01893 A typical feedstock is reported below.

TABLE 1 TYPICAL CDW FEEDSTOCK API Gravity Pour Point, *C 29 Aniline Point, 'C 82 K Factor 11.8 Distillation, °C (D-1160) 333 356 371 389 427 29.4 (180) (0.880g/cm 3 (631) (672) (699) (733) (800) Although the operation of the CDW reactor section is similar to a hydrodesulfurizer (HDS), that is, oil and hydrogen are passed over a fixed bed of catalyst, the disposition of the products and by-products is different. The unsaturated light liquid hydrocarbons from the stabilizer are sent to the FCC gas plant for further recovery. The butenes become alkylation feed. Propenes are polymerized. The CDW naphtha is sent directly to gasoline blending.

The distillate product is blended directly to diesel fuel, and the bottoms are recycled to the FCC unit.

Direct blending of CDW naphtha into the gasoline pool is possible because of its high octane number (typically 92 RONC) and low mercaptan level. Table 2 lists the properties of this stream.

Caustic and water washing equipment were added to the unit to handle high mercaptan levels, but the low sulfur crudes run to date have made WO 91/15561 PCT/US9/01893 -21 it unnecessary to use the facilities. If high sulfur crudes are processed, this equipment will have to be activated.

TABLE 2 TYPICAL CDW GASOLINE PRODUCT PFOPERTIES (1) Properties API Gravity Sulfur, wt.% Mercaptans, ppmw Bromine Number 70 0.01 140 (0.70 g/cm 3 Octanes RON-Clear MON-Clear Composition, )Vol.% Paraffins Olefins Naphthenes Aromatics Distillation. *F (D-86) Vol% Vol% Vol% Vol% Vol% Vol% Vol% (115) (130) (155) (180) (220) (275) (300) (325) Derived from waxy crudes Debutanized sample The CDW diesel oil is a blend of side draws from the splitter and the vacuum flash unit. The target pour point is typically -5.6'C but it is adjusted to WO 91/15561 PCT/US90/01 893 -22 meet pool fluidity requirements. The low pour point CDW product is blended with FCC light cycle oil and virgin distillates to meet No. 2 and diesel fuel specifications.

Properties of these three blending stocks are shown on Table 3.

TABLE 3 PROPERTIES OF DIESEL BLENDING COMPONENTS (1) Properties API Gravity (g/cm 3 Sulfur, wt% Nitrogen, ppmw Basic Nitrogen, ppmw Kinematic Vis. 40*C, cs Kinematic Vis. 100*C, cs Flash Point (COC), *C Carbon Residue, wt% Aniline Point, *C Bromine Number Cetane Index

CDW

Distillate 28.0 (0.886) 0.12 250 102 6.92 2.04 66 (150) 0.01 66 (150) 9.0 48

LAGO

35.7 (0.847) 0.08 68 47 3.16 1.26 90 (194) 0.03 69 (156) 0.9 54 28.7 (0.883) 0.10 140 72 2.79 1.13 66 (150) 0.01 52 (125) 12 Fluidity Pour Point, *C Cloud Point, 'C Distillation. 'C (D-86)

IBP

Vol% Distilled Vol% Distilled Vol% Distilled 50 Vol% Distilled Vol% Distilled Vol% Distilled Vol% Distilled

EP

Derived from waxy crudes -23 (-10) -18 (0) -12 (10) -10 (14) -12 -8 (18) (348) (435) (479) (587) (618) (641) (671) (685) (701) (359) (425) (449) (503) (535) (564) (602) (625) (650) 202 210 244 244 267 292 323 335 348 (396) (410) (472) (472) (512) (558) (614) (635) (659) WO 91/15561 PC7F/US90/01893 -23 CDW Catalyst Aqing As shown on Figure 2, the catalyst has an initial high aging rate, but then it lines out to provide a long cycle. The temperature variations on Figure 2 are due to the many shifts in crude quality that the refinery experiences. Variations due to throughput (space velocity) and product pour point have been accounted for by normalizing the data to a pour point of -23*C (minus and a design throughput of 2700 m 3 per stream day (17,000 BPSD). FCC variations as well as crude shifts have not been accounted for in normalizing the data.

When the CDW unit was streamed some downstream fractionation equipment was not ready for operation.

These were commissioned later in the first cycle. The run length for this cycle exceeded six months. The second cycle was cut short due to a scheduled crude unit turn around.

A hot hydrogen reheat line was added before the start of the third cycle. There was also an improvment in virgin feed quality, because of the crude unit modifications. With hot hydrogen reheat, and better feed, the third cycle length was increased to 264 days on stream.

Figure 2, cycle 3 thus shows operation with distributed flow of H 2 recycle gas. Cycle 1 and cycle 2 represent prior art dewaxing processes, all the recycle H 2 enters reactor 10. Cycle 3 represents the present invention, namely distributed H 2 recycle. This was achieved by adding 196-214 vol/vol feed (1100-1200 SCFB) of hot, H 2 rich gas to the Rx 1 effluent. This also increased the inlet temperature 3.8 to 19.4*C (7 to depending on charge rate, to the second stage dewaxing reactor WO 91/15561 PCr/US90/0193 -24 The riin effect to be noted in Figure 2, cycle 3 is that from reheating the first reactor effluent, rather than a shift in recycle H 2 distribution. The run did not last long enough to make us want to cut back on H 2 addition rates to the first reactor.

Although the data show quite a lot of scatter, as is to be expected in commercial units, the data nonetheless show that much longer cycle lengths (reduced catalyst aging rates) can be achieved by conducting the dewaxing process in at least two stages, with hot hydrogen addition to the second stage.

Claims (13)

1. A process for the shape selective catalytic dewaxing of a wax containing feed comprising at least one of atmospheric gas oil and vacuum gas oil by passing the feed in admixture with 180 to 890 vol/vol feed (1000 to 5000 SCFB) of hydrogen over a dewaxing catalyst comprising a shape selective zeolite to produce a dewaxed product and wherein the hydrogen is added to retard catalyst aging, characterized by conducting the dewaxing reaction in at least two stages, with a first stage containing at least 20 wt.% of the dewaxing catalyst and in at least one second stage containing at least 20 wt.% of the dewaxing catalyst and adding at least a portion of the hydrogen downstream of the first stage reactor.

2. The process of claim 1 wherein hydrogen is added downstream of the first stage after the first stage catalyst is partially deactivated.

3. The process of claim 1 wherein hydrogen addition to the first stage is reduced to less than 360 vol/vol feed (2000 SCFB) and hydrogen addition to the second stage is increased to 50-270 vol/vol feed (300-1500 SCFB), after the first stage catalyst contains at least 5.j wt.% coke.

4. The process of claim 3 wherein H 2 addition to the first stage is reduced to 130-270 vol/vol feed (750-1500 SCFB) and H 2 addition to the second stage is increased to 90-270 vol/vol feed (500-1500 SCFB). The process of claim 1 wherein at least wt.% of the feed is cracked to gasoline boiling range product having a research clear octane number of at least SUBSTITUTE SHEET IpEANUS P-5120 -26- 14 Rec'd PCT/PTO 2 APR SPF/S9f /01 893

6. The process of claim 1 wherein at least wt.% of the feed is cracked to a gasoline boiling range product having a research clear octane number of at least 92.

7. The process of claim 1 wherein the zeolite is selected from ZSM-5, ZSM-11, ZSM-12, ZSM-23, ZSM-38 and ZSM-48.

8. The process of claim 1 wherein the zeolite is

9. The process of claim 1 wherein the feed has a pour point of at least 240'C A process for the selective cracking of wax in a heavy feed boiling above the gasoline boiling range in admixture with 180 to 890 vol/vol feed (1000-5000 SCFB) hydrogen over a shape selective zeolite wax cracking catalyst at a temperature in excess of 360'C to produce a dewaxed heavy feed and a gasoline boiling range product having a research clear octane number of at least 90 and deactivated catalyst containing coke, characterized by hydrocracking the wax in at least a first stage reaction zone containing at least 20 wt.% of the catalyst and at least a second stage reaction zone containing at least 20 wt.% of the catalyst, and adding at least 10% of the hydrogen to the first stage effluent. SUBS ITUTE SHEET PENUS fW it r J WO 91/15561 PCT/US90/01 893 -27

11. The process of claim 10 wherein hydrogen addition to the first stage is reduced to less than 360 vol/vol feed (2000 SCFB) and hydrogen addition to the second stage is increased to 50-270 vol/vol feed (300-1500 SCFB), after the first stage catalyst contains at least 5.0 wt.% coke.

12. The process of claim 11 wherein H 2 addition to the first stage is reduced to 130-270 vol/vol feed (750-1500 SCFB) and H 2 addition to the second stage is increased to 90-270 vol/vol feed 500-1500 SCFB).

13. The process of claim 10 wherein at least wt.% of the feed is cracked to gasoline boiling range product having a research clear octane number'of at least

14. The process of claim 10 wherein .t least wt.% of the feed is cracked to a gasoline boiling range product having a research clear octane number of at least

92. The process of claim 10 wherein the zeolite is selected from the group consisting of ZSM-5, ZSM-11, ZSM-12, ZSM-23, ZSM-35, ZSM-38 and ZSM-48. 16. The process of claim 10 wherein the catalyst comprises 17. The process of claim 10 wherein the feed has a pour point of at least 24*C 27a- 18. A process according to claim 1 substantially as hereinbefore described with reference to the example. DATED: 16 June 1993 PHILLIPS ORMONDE FITZPATRICK Patent Attorneys For: MOBIL OIL CORPORATION dp (5546h)