CA2047075A1 - Low pour high vi lubes via co-processing solvent dewaxing - Google Patents
Low pour high vi lubes via co-processing solvent dewaxingInfo
- Publication number
- CA2047075A1 CA2047075A1 CA 2047075 CA2047075A CA2047075A1 CA 2047075 A1 CA2047075 A1 CA 2047075A1 CA 2047075 CA2047075 CA 2047075 CA 2047075 A CA2047075 A CA 2047075A CA 2047075 A1 CA2047075 A1 CA 2047075A1
- Authority
- CA
- Canada
- Prior art keywords
- oil
- boiling
- dewaxing
- point
- low
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/02—Petroleum fractions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G73/00—Recovery or refining of mineral waxes, e.g. montan wax
- C10G73/02—Recovery of petroleum waxes from hydrocarbon oils; Dewaxing of hydrocarbon oils
- C10G73/06—Recovery of petroleum waxes from hydrocarbon oils; Dewaxing of hydrocarbon oils with the use of solvents
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Lubricants (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
High boiling high VI wax isomerates and natural waxy oil distillates can be solvent dewaxed to low pour point under miscible conditions by combining said high boiling high VI stocks with from 5 to 50 LV%
of a lower boiling conventional VI waxy lube oil and co-processing the mixture under conventional solvent dewaxing conditions. The resultant low pour mixture can subsequently be fractionated into high yields of the high boiling high VI component and of the lower boiling, conventional VI component, both components exhibiting low pour points.
High boiling high VI wax isomerates and natural waxy oil distillates can be solvent dewaxed to low pour point under miscible conditions by combining said high boiling high VI stocks with from 5 to 50 LV%
of a lower boiling conventional VI waxy lube oil and co-processing the mixture under conventional solvent dewaxing conditions. The resultant low pour mixture can subsequently be fractionated into high yields of the high boiling high VI component and of the lower boiling, conventional VI component, both components exhibiting low pour points.
Description
~ 17~
Backaround of the Invention Solvent dewaxing of waxy lube oils has long been known. It has also been known that lighter oils, oils of lower boiling point and VI of about 90-105/110 are more miscible in dewaxing solvents of a given composition than are higher boiling-higher VI oils. It is also widely accepted that good yields of dewaxed oils are obtained when the dewaxing procedure is practiced under oil/solvent miscible conditions. To this end, conditions of solvent to oil ratios, dewaxing temperatures and solvent/cosolvent ratios have been adjusted to achieve oil-solvent miscibility at the dewaxing temperature (filter temperature). All too often, however, a compromise must be struck between yield of dewaxed oil and pour point, that is low pour points are achieved at the expense of product yield or conversely high yields are achieved at the price of higher pour point.
U.S. Patent 3,365,390 describes a lube oil production process involving hydrocracking a heavy oil feed, separating hydrocracked wax from a hydrocracked lubricating oil portion of the products and hydroiso-merizing the hydrocracked wax using an active reforming catalyst. An isomerized lubricating oil fraction so produced can be dewaxed separately, to recover ultra high VI isomerized lube oil, or the isomerized lube oil fraction is dewaxed in admixture with a hydrocracXed lubricating oil fraction. When the isomerate is dewaxed in combination with a hydrocracked lube oil fraction the wax recovered is a mixture of hydrocracked wax and isomerized wax and the properties of the - 2 - 2 ~ -~ 7~ 7 ~
recovered lube oil are upgraded due to the presence of the isomerate lube oil portion.
High boiling-high VI wax isomerate and natural waxy oil distillates are difficult to dewax to achieve pour point in the reg-ion of about -20C and lower. Such oils when solvent dewaxed to low tempera-ture typically encounter oil/solvent miscibility problems resulting in poor dewaxed oil yields.
Descri~tion of the Invention It has been discovered that high boiling high VI oils can be solvent dewaxed to low pour point under miscible conditions when using low miscibility dewaxing solvents, e.g. C3-C6 ketone based dewaxing solvents such as methyl ethyl ketone, methyl isobutyl ketone, acetone, etc. and mixtures thereof such as MEK/MIBK by combining a quantity of low boiling conventional VI
waxy oil with the high boiling high VI oil and co-processing the mixture under conventional solvent dewaxing conditions. The addition of the low boiling conventional VI waxy oil to the high boiling high VI
oil permits dewaxing to be conducted under miscible conditions resulting in the production of acceptable yields of low pour point dewaxed oil. It has further been discovered that the low pour point dewaxed oil mixture may be subsequently fractioned into fractions whose specifications are very close to the parent materials in terms of boiling point and VI and that both such fractions possess the low pour point of the mixture. Upon normalization of yields it has been discovered that the yield of the low pour-high boiling-high VI oil fraction achieved by the co-processing procedure is higher than that achieved when the high boiling high VI oil is dewaxed by itself.
Backaround of the Invention Solvent dewaxing of waxy lube oils has long been known. It has also been known that lighter oils, oils of lower boiling point and VI of about 90-105/110 are more miscible in dewaxing solvents of a given composition than are higher boiling-higher VI oils. It is also widely accepted that good yields of dewaxed oils are obtained when the dewaxing procedure is practiced under oil/solvent miscible conditions. To this end, conditions of solvent to oil ratios, dewaxing temperatures and solvent/cosolvent ratios have been adjusted to achieve oil-solvent miscibility at the dewaxing temperature (filter temperature). All too often, however, a compromise must be struck between yield of dewaxed oil and pour point, that is low pour points are achieved at the expense of product yield or conversely high yields are achieved at the price of higher pour point.
U.S. Patent 3,365,390 describes a lube oil production process involving hydrocracking a heavy oil feed, separating hydrocracked wax from a hydrocracked lubricating oil portion of the products and hydroiso-merizing the hydrocracked wax using an active reforming catalyst. An isomerized lubricating oil fraction so produced can be dewaxed separately, to recover ultra high VI isomerized lube oil, or the isomerized lube oil fraction is dewaxed in admixture with a hydrocracXed lubricating oil fraction. When the isomerate is dewaxed in combination with a hydrocracked lube oil fraction the wax recovered is a mixture of hydrocracked wax and isomerized wax and the properties of the - 2 - 2 ~ -~ 7~ 7 ~
recovered lube oil are upgraded due to the presence of the isomerate lube oil portion.
High boiling-high VI wax isomerate and natural waxy oil distillates are difficult to dewax to achieve pour point in the reg-ion of about -20C and lower. Such oils when solvent dewaxed to low tempera-ture typically encounter oil/solvent miscibility problems resulting in poor dewaxed oil yields.
Descri~tion of the Invention It has been discovered that high boiling high VI oils can be solvent dewaxed to low pour point under miscible conditions when using low miscibility dewaxing solvents, e.g. C3-C6 ketone based dewaxing solvents such as methyl ethyl ketone, methyl isobutyl ketone, acetone, etc. and mixtures thereof such as MEK/MIBK by combining a quantity of low boiling conventional VI
waxy oil with the high boiling high VI oil and co-processing the mixture under conventional solvent dewaxing conditions. The addition of the low boiling conventional VI waxy oil to the high boiling high VI
oil permits dewaxing to be conducted under miscible conditions resulting in the production of acceptable yields of low pour point dewaxed oil. It has further been discovered that the low pour point dewaxed oil mixture may be subsequently fractioned into fractions whose specifications are very close to the parent materials in terms of boiling point and VI and that both such fractions possess the low pour point of the mixture. Upon normalization of yields it has been discovered that the yield of the low pour-high boiling-high VI oil fraction achieved by the co-processing procedure is higher than that achieved when the high boiling high VI oil is dewaxed by itself.
- 3 - 2~7~
Description of the Figures Fiaure 1 compares the miscibility of heavy, high boiling high VI wax isomerate oil to that of a mixture of said heavy oil with a light oil at a 2/1 ratio in ketone dewaxing solvents of varying propor-tions at different temperatures.
iaure 2 shows the yield of -21-C pour dewaxed oil derived from Fischer-Tropsch isomerate, the yield being normalized to 100 barrels of Fischer-Tropsch isomerate feed to the dewaxer on the basis of both neat Fischer-Tropsch isomerate and a Fischer-Tropsch isomerate/150N blend.
The Invention Heavy, high boiling, high VI waxy oils, be they waxy oils obtained by wax isomerization or conven-tional oils, such as deaspha}ted 600N hydrocracked oil, or Bright Stocks which are immiscible in typical low miscibility dewaxing solvents such as C3-C6 ketones at the low dewaxing temperature used when low pour points of about -21C are sought can be solvent dewaxed to a target pour point of about -21-C and lower, preferably about -24-C, most preferably about -27-C using conven-tional solvents under miscible conditions (e.g. a filter temperature of no less than about -35-C so as to have a pour/filter ~T of about 3-4-C or less) by adding to the heavy, high boiling, high VI waxy oil a quantity of lower boil~ng conventional VI waxy oil distillate and processing this mixture through the solvent dewax-ing process under miscible conditions.
The light lower boiling conventional VI waxy oil added to the heavy, high boiling high VI waxy oil will be such that it can be easily separated from the _ 4 _ 2 ~ ~ 7 ? ,~
heavy oil by distillation, therefore it will be charac-terized by possessing a 90% off point about 50-300F, preferably 50-100F, lower than the 10% off point of the heavy oil. The bulk of the light oil is substan-tially lighter and lower boiling than the bulk of the heavy oil.
The light oil is added to the heavy oil in an amount sufficient to render the mixture miscible in the low miscibility dewaxing solvent used at a filter temperature which permits the waxy oil to possess a pour point of at least -21~C, preferably about -24C, most preferably about -27-C. The amount of added light oil can range between about g to 50% by vol. of the oil mixture, preferably about 20 to 40 vol.%.
The solvent dewaxing process which is bene-fited by operating on the dual component waxy feed stock is any typical solvent dewaxing process including those identified as dilution indirect chilling process-es, pre-dilution direct chilling processes or just direct chilling processes.
Indirect chillinq processes include, for example, scraped surface chilling processes wherein the waxy oil charge is diluted with solvent to produce a solution which is passed through the scraped surface chiller wherein a refrigerant is passed through the outer jacket of the heat exchanger while a rotating scraper blade prevents wax build up in the inner surface of the chiller.
Direct chilling processes can employ either no dilution or predilution of the waxy charge. The waxy charge with or without dilution is then chilled by the injection of cold solvent directly into the waxy charge.
- 5 - ~J~
A preferred embodiment of dilution chilling is the DILCHILL process wherein the waxy charge is passed through a chilling tower divided into stages and cold solvent is injected into a number of said stages.
In those stages into which cold solvent is injected, a high level of agitation is maintained CO that substan-tially instantaneous mixing of the chilling solvent and waxy oil is achieved thereby avoiding detrimental shock chilling. This procedure i8 described in greater detail in U.S. Patent 3,773,650. In an alternate embodiment the waxy oil i8 chilled to a temperature about 35F above the filter temperature in the appara~
tus described above, with chilling down to the filter temperature being performed in a subsequent scraped surface chiller. This embodiment is described in U.S.
Patent 3,775,288.
The low miscibility dewaxing solvents which are typically used in solvent dewaxing processes and which are the same solvents which are used in the process of the present invention include C3-C6 ketones such acetone, methyl ethyl ketone (MEK), methyl isobutyl ketone (MIBK) and mixtures thereof, such as MEK/MIBK.
The heavy high boiling high VI waxy oil can be that material obtained by isomerizing wax either synthetic wax as is obtained from Fischer-Tropsch synthesis or natural wax as i8 obtained by dewaxing hydrocarbon oil8, commonly called slack wax or a natural petroleum material ~uch as hydrocracked oil, deasphalted 600N or, Bright Stock oil. When the waxy oil to be dewaxed is a heavy high boiling high VI wax isomerate, it is preferred that the total fraction of oil boiling in the lube oil boiling range (i.e. about 330-C and above preferably about 370C and above) be the feed to the dewaxing process of the present - 6 - 2~-17~7~
invention, i.e. utilizes the addition of a light oil fraction to facilitate dewaxing under miscible condi-tions. In general heavy-high boiling-high VI materials be they isomerates natural oils, or hydrocracked oils are those materials having a viscosity in the range 6 to 12 cSt 0 100C, preferably 8 to 10 cSt ~ 100C, a mid LV% boiling point of 450 to 5507C, preferably 475 to 525C and a VI of at least 120, preferably at least 140.
The light, lower boiling lower VI oil is one having a viscosity of about 3 to 7 cSt @ 100C, prefer-ably about 4 to 6 cSt ~ 100C, a 90% off point about 0 to 300F, preferably about 50 to 100F, lower than the 10% off point of the heavy oil and a VI of less than about 110, preferably less than about 100.
In the process of the present invention the heavy oil is mixed with a volume of light oil to permit operation of the solvent dewaxing process under miscible conditions at a filter temperature low enough to produce an oil having a pour point of at least -21C.
After processing the mixed oil feed through the solvent dewaxing process the resulting dewaxed oil product is fractionated into fractions corresponding very closely to the original parent materials (i.e. a light oil fraction of conventional VI and a heavy oil fraction of high VI). Each of these fractions possess-es a pour point of at lea~t about -21-C, the pour point of the mixture. The yield of heavy oil of -21C pour obtained by this co-processing technique is higher than that achievable by processing the heavy oil by itself.
The wax which is isomerized may come from any of a number of sources. Synthetic waxes from Fischer-2 ~ :~ 7~ 7~3 Tropsch processes may be used, as may be waxes recov-ered from the solvent or autorefrigerative dewaxing of conventional hydrocarbon oils as well as mixtures of these waxes. Waxes from dewaxing conventional hydro-carbon oils are commonly called slack waxes and usually contain an appreciable amount of oil. The oil content of these slack waxes can range anywhere from 0 to 45%
or more, usually 5 to 30~ oil. For the purposes of this application, the heavy waxes recovered from the dewaxing of Bright Stock and the heavy Fischer-Tropsch waxes are the feeds of choice.
Hydroisomerization may be performed over any of the standard hydroisomerization catalysts which contain a hydrogenation metal selected from Group VIB
and ~roup VIII and mixtures thereof, preferably the Group VIII metals, more preferably the noble Group VIII
metals, most preferably platinum. Metal loading ranges between 0.1 to 5.0 wt% metal, preferably 0.1 to 1.0 wt%
metal, most preferably 0.2 to 0.6 wt% metal.
The hydrogenation metal component is support-ed on a refractory inorganic metal oxide support, preferably alumina or silica-alumina, most preferably the transition aluminas, e.g., gamma alumina. Prefer-ably the support is halogenated. The halogen is usually chlorine or fluorine or mixture thereof, preferably fluorine, with net halogen content in the range 1 to 10 wt%, preferably 2 to 8 wt%.
Isomerization i8 conducted under conditions of temperature between about 250 to 400C, preferably 270-360~C, pressures of 500 to 3000 psi H2, preferably 1000-1500 psi H2, hydrogen gas rates of 1000 to 10,000 SCF/bbl, and a space velocity in the range 0.1-10 v/v/hr, preferably 1-2 v/v/hr.
- ~ - 2~ ~7~ ~
Preferred catalysts are the subject of u.S.
Patent 4,959,337, U. S . Patent 4,906,601 and U.S. Patent 4,900,707.
The use of these catalysts for the production of a lube oil base stock or blending stock by the isomerization of wax is the subject of U.S. Patent 4,929,795, U. S . Patent 4,923,588, and U.S. Patent 4,937,399 respectively.
A most preferred catalyst is the subject of U.S. Patent 4, 906,601. The use of that catalyst for wax isomerization is the subject of U.S. Patent 4,923,588.
That catalyst comprises a noble Group VIII
metal on low fluoride content small particle size refractory metal oxide base. The catalyst is charac-terized by having a fluoride content in the range of 0.1 to up to but less than 2 wt%, preferably 0.1 to 1. 5 wt%, more preferably 0.2 to 1.0 wt%, a particle diame-ter of less than 1/16 inch and a preferred noble Group VIII metal loading in the range of 0.1 to 2.0 wt~. The preferred small particle æupport is 1/20 inch trilobe alumina.
As one would expect, noble metal isomeriza-tion catalysts are extremely susoeptible to deactiva-tion by the presence of heteroatom compounds (i.e. N, O
or S compound~) in the wax feed 80 care mu~t be exer-cised to remove such heteroatom materials from the wax feed charge6. When dealing with high purity waxes such as synthetic Fischer-Tropsch waxes, such precautions may not be necessary. In such cases, subjecting such waxes to very mild hydrotreating may be sufficient to insure protection for the isomerization catalyst. On the other hand, waxes obtained from natural petroleum -- 9 -- 2 ~ ~ r~ ~ r~ ~3 sources contain quantities of heteroatom compounds as well as appreciable quantities of oil which contain heteroatom compoundsO In such instances the slack waxes should be hydrotreated to reduce the level of heteroatom compounds to levels commonly accepted in the industry as tolerable for feeds to be exposed to isomerization catalysts. Such levels will typically be a N content of about 1 to 5 ppm and a S content of about 1 to 20 ppm, preferably 2 ppm or less nitrogen and 5 ppm or less sulfur. Similarly, such slack waxes prior to hydrotreating should be deoiled to an oil content in the range of 0 to 35% oil, preferably 5 to 25% oil. The hydrotreating step will employ a typical hydrotreating catalyst such as Co/Mo or Ni/Mo on alumina under standard, commercially acceptable condi-tions, e.g., temperature of 280 to 400C, space veloci-ty of 0.1 to 2.0 V/V/hr, pressure of from 500 to 3000 psig H2 and hydrogen gas rates of from 500 to 5000 SCF/bbl.
The present invention will be better under-stood by reference to the following non-limiting examples.
Figure 1 shows how the miscibility of a Fischer-Tropsch 8.7 cSt Q100C isomerate fraction boiling in the 550 to 575C range (about equivalent to a 250N viscosity grade) can be improved about 10C with the addition of 33% of a conventional 150N basestock.
Filtration studies were performed with this combined feedstock and compared with base case evaluation of the neat Fischer-Tropsch 8.7 cSt ~lOO-C wax isomerate. The isomerate was made by isomerizing a Fischer-Tropsch 150 wax as feed over an isomerization catalyst comprising 0.6 Pt/5.6% F/A12O3 at a temperature between 365 to 375C, a pressure of 1000 psig, a H2 flow rate of 7500 - lo - 2~.17~7~
SCF H2/bbl and a LHSV of 1. The dewaxing data are given in Table 1.
In an effort to reach the -21C pour target, solvent composition of the MEK/MIBK system was lowered to 10~ MEK and the dewaxing of 100% Fischer-Tropsch 8.7 cSt QlOO-C wax isomerate was performed at a filter temperature just below miscibility (degrees from miscibility -3). Typical of immiscible dewaxing, the process gave a low pour filter temperature spread and high filter rates. However, as is normally experienced with immiscible dewaxing, the wash efficiency with two liquid phases is very poor and the resulting low yield of 15.7 wt% is unacceptable. Although not measured directly it is calculated, based on typical immiscible isomerate dewaxing data that the product had a VI of about 158, a viscosity at 100C of about 8.0 cSt. It has been observed that on going from miscible dewaxing to immiscible dewaxing a viscoæity decrease is common while VI shows very little change.
Going to miscible dewaxing, as was done in the second case by raising the filtration temperature, raised the yields to acceptable levels but the attain-able pour point was raised to only -lO-C.
Using a blend of conventional 150N oil and Fischer-Tropsch 8.7 cSt ~lOO-C wax isomerate the Pilter temperature can be lowered below the target pour without immiscibility occurring. Low pours ~-21'C) were achieved at good yields. The lower filtration rate of 5.2 m3/M2d is not necessarily cause for concern as plants running 600N stocks are typically designed for filter rates of 4 to 6 m3/m2d and techniques to ; handle these rates are known.
:
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As one might expect, the product from the dewaxer is a mixture of conventional and non-conven-tional lube. Crucial to the process is the successful separation of the light dewaxed oil from the heavy dewaxed oil e.g. the light conventional oil from the heavier isomerate oil. While any separation process (distillation, extraction, membranes, etc.) could be considered, the simplest and most straight forward process is distillation. For that reason low boiling conventional lubes are co-processed with the relatively high boiling isomerate oils. It is interesting to note that this does not imply a wide difference in viscosity grades. Due to the highly paraffinic nature of the isomerate oil it has a much higher boiling point than equivalent viscosity conventional stocks. This differ-ence in the viscosity/boiling point relationship makes the separation of a 5.0 cSt 150N oil and a 8.7 cSt Fischer Tropsch wax isomerate quite feasible as demon-strated in Table 2.
The dewaxed oil product from the co-process-ing was cut into fractions which were then reblended to roughly the same specifications as would be possessed by individually processed dewaxed oil fractions (See Table 2).
Using the 40% to Final Boiling Point blend, a 9.2 cSt, 148 VI, -22C pour product was made, leaving a 102 VI, 4.7 cSt, -22-C pour conventional stock. These specifications are very close to the parent materials.
Surprisingly it has been found that not only is the dewaxing of the heavy oil fraction made easier by the procedure of dewaxing a heavy oil/light oil blend, but also the yield of dewaxed heavy oil is higher. Thus, while 100 barrels of Fischer-Tropsch isomerate can be dewaxed to give 15.7 barrels of -21C pour oil (15.7 LV%, see Table 1), when these same 100 barrels of Fischer-Tropsch isomerates are mixed with 50 barrels of 150N oil (to give a total of 150 barrels of oil to be dewaxed) a total dewaxed oil yield of 49.3% is obtained l74 barrels DW0 based on 150 barrels mixture) and upon fractionation 60% or 44.4 barrels (60% of 74 barrels) is found to constitute the amount of oil having a VI, viscosity and pour corresponding to the 15.7 barrels obtained when the Fischer-Tropsch isomerate was dewaxed by itself. Thus, yield of the premium quality high VI
oil is increased at the same time the dewaxing is made easier (See Figure 2).
This yield increase is much greater than what one would obtain from simply mixing fractions of separately dewaxed FT isomerate and 150N oil. Linear blending of such fractions to give a final product with a ~48 VI would require a mixture of 84 LV% FT
isomerate/16 LV% 150N. This blend would produce a yield of only 18.7% compared to the about 44% of 148 VI
product obtained by co-processing. The oil product obtained by linear blending would also be of different quality. Whereas coprocessing gives a yield of 44.4%
of a 148 VI, 55.21 cSt Q 40-C, 9.19 cSt Q 100C mate-rial, linear blending would produce an 18.7% yield of a 148 VI, 44.78 cSt 0 40-C, 7.9 cSt Q lOO-C product.
Furthermore, coprocessing followed by fractionation produces a light oil of 102 VI and 5 Vis which is obviously superior to the base 150N oil fraction which, when separately dewaxed produced a DW0 of 90 VI and 5 vis .
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Description of the Figures Fiaure 1 compares the miscibility of heavy, high boiling high VI wax isomerate oil to that of a mixture of said heavy oil with a light oil at a 2/1 ratio in ketone dewaxing solvents of varying propor-tions at different temperatures.
iaure 2 shows the yield of -21-C pour dewaxed oil derived from Fischer-Tropsch isomerate, the yield being normalized to 100 barrels of Fischer-Tropsch isomerate feed to the dewaxer on the basis of both neat Fischer-Tropsch isomerate and a Fischer-Tropsch isomerate/150N blend.
The Invention Heavy, high boiling, high VI waxy oils, be they waxy oils obtained by wax isomerization or conven-tional oils, such as deaspha}ted 600N hydrocracked oil, or Bright Stocks which are immiscible in typical low miscibility dewaxing solvents such as C3-C6 ketones at the low dewaxing temperature used when low pour points of about -21C are sought can be solvent dewaxed to a target pour point of about -21-C and lower, preferably about -24-C, most preferably about -27-C using conven-tional solvents under miscible conditions (e.g. a filter temperature of no less than about -35-C so as to have a pour/filter ~T of about 3-4-C or less) by adding to the heavy, high boiling, high VI waxy oil a quantity of lower boil~ng conventional VI waxy oil distillate and processing this mixture through the solvent dewax-ing process under miscible conditions.
The light lower boiling conventional VI waxy oil added to the heavy, high boiling high VI waxy oil will be such that it can be easily separated from the _ 4 _ 2 ~ ~ 7 ? ,~
heavy oil by distillation, therefore it will be charac-terized by possessing a 90% off point about 50-300F, preferably 50-100F, lower than the 10% off point of the heavy oil. The bulk of the light oil is substan-tially lighter and lower boiling than the bulk of the heavy oil.
The light oil is added to the heavy oil in an amount sufficient to render the mixture miscible in the low miscibility dewaxing solvent used at a filter temperature which permits the waxy oil to possess a pour point of at least -21~C, preferably about -24C, most preferably about -27-C. The amount of added light oil can range between about g to 50% by vol. of the oil mixture, preferably about 20 to 40 vol.%.
The solvent dewaxing process which is bene-fited by operating on the dual component waxy feed stock is any typical solvent dewaxing process including those identified as dilution indirect chilling process-es, pre-dilution direct chilling processes or just direct chilling processes.
Indirect chillinq processes include, for example, scraped surface chilling processes wherein the waxy oil charge is diluted with solvent to produce a solution which is passed through the scraped surface chiller wherein a refrigerant is passed through the outer jacket of the heat exchanger while a rotating scraper blade prevents wax build up in the inner surface of the chiller.
Direct chilling processes can employ either no dilution or predilution of the waxy charge. The waxy charge with or without dilution is then chilled by the injection of cold solvent directly into the waxy charge.
- 5 - ~J~
A preferred embodiment of dilution chilling is the DILCHILL process wherein the waxy charge is passed through a chilling tower divided into stages and cold solvent is injected into a number of said stages.
In those stages into which cold solvent is injected, a high level of agitation is maintained CO that substan-tially instantaneous mixing of the chilling solvent and waxy oil is achieved thereby avoiding detrimental shock chilling. This procedure i8 described in greater detail in U.S. Patent 3,773,650. In an alternate embodiment the waxy oil i8 chilled to a temperature about 35F above the filter temperature in the appara~
tus described above, with chilling down to the filter temperature being performed in a subsequent scraped surface chiller. This embodiment is described in U.S.
Patent 3,775,288.
The low miscibility dewaxing solvents which are typically used in solvent dewaxing processes and which are the same solvents which are used in the process of the present invention include C3-C6 ketones such acetone, methyl ethyl ketone (MEK), methyl isobutyl ketone (MIBK) and mixtures thereof, such as MEK/MIBK.
The heavy high boiling high VI waxy oil can be that material obtained by isomerizing wax either synthetic wax as is obtained from Fischer-Tropsch synthesis or natural wax as i8 obtained by dewaxing hydrocarbon oil8, commonly called slack wax or a natural petroleum material ~uch as hydrocracked oil, deasphalted 600N or, Bright Stock oil. When the waxy oil to be dewaxed is a heavy high boiling high VI wax isomerate, it is preferred that the total fraction of oil boiling in the lube oil boiling range (i.e. about 330-C and above preferably about 370C and above) be the feed to the dewaxing process of the present - 6 - 2~-17~7~
invention, i.e. utilizes the addition of a light oil fraction to facilitate dewaxing under miscible condi-tions. In general heavy-high boiling-high VI materials be they isomerates natural oils, or hydrocracked oils are those materials having a viscosity in the range 6 to 12 cSt 0 100C, preferably 8 to 10 cSt ~ 100C, a mid LV% boiling point of 450 to 5507C, preferably 475 to 525C and a VI of at least 120, preferably at least 140.
The light, lower boiling lower VI oil is one having a viscosity of about 3 to 7 cSt @ 100C, prefer-ably about 4 to 6 cSt ~ 100C, a 90% off point about 0 to 300F, preferably about 50 to 100F, lower than the 10% off point of the heavy oil and a VI of less than about 110, preferably less than about 100.
In the process of the present invention the heavy oil is mixed with a volume of light oil to permit operation of the solvent dewaxing process under miscible conditions at a filter temperature low enough to produce an oil having a pour point of at least -21C.
After processing the mixed oil feed through the solvent dewaxing process the resulting dewaxed oil product is fractionated into fractions corresponding very closely to the original parent materials (i.e. a light oil fraction of conventional VI and a heavy oil fraction of high VI). Each of these fractions possess-es a pour point of at lea~t about -21-C, the pour point of the mixture. The yield of heavy oil of -21C pour obtained by this co-processing technique is higher than that achievable by processing the heavy oil by itself.
The wax which is isomerized may come from any of a number of sources. Synthetic waxes from Fischer-2 ~ :~ 7~ 7~3 Tropsch processes may be used, as may be waxes recov-ered from the solvent or autorefrigerative dewaxing of conventional hydrocarbon oils as well as mixtures of these waxes. Waxes from dewaxing conventional hydro-carbon oils are commonly called slack waxes and usually contain an appreciable amount of oil. The oil content of these slack waxes can range anywhere from 0 to 45%
or more, usually 5 to 30~ oil. For the purposes of this application, the heavy waxes recovered from the dewaxing of Bright Stock and the heavy Fischer-Tropsch waxes are the feeds of choice.
Hydroisomerization may be performed over any of the standard hydroisomerization catalysts which contain a hydrogenation metal selected from Group VIB
and ~roup VIII and mixtures thereof, preferably the Group VIII metals, more preferably the noble Group VIII
metals, most preferably platinum. Metal loading ranges between 0.1 to 5.0 wt% metal, preferably 0.1 to 1.0 wt%
metal, most preferably 0.2 to 0.6 wt% metal.
The hydrogenation metal component is support-ed on a refractory inorganic metal oxide support, preferably alumina or silica-alumina, most preferably the transition aluminas, e.g., gamma alumina. Prefer-ably the support is halogenated. The halogen is usually chlorine or fluorine or mixture thereof, preferably fluorine, with net halogen content in the range 1 to 10 wt%, preferably 2 to 8 wt%.
Isomerization i8 conducted under conditions of temperature between about 250 to 400C, preferably 270-360~C, pressures of 500 to 3000 psi H2, preferably 1000-1500 psi H2, hydrogen gas rates of 1000 to 10,000 SCF/bbl, and a space velocity in the range 0.1-10 v/v/hr, preferably 1-2 v/v/hr.
- ~ - 2~ ~7~ ~
Preferred catalysts are the subject of u.S.
Patent 4,959,337, U. S . Patent 4,906,601 and U.S. Patent 4,900,707.
The use of these catalysts for the production of a lube oil base stock or blending stock by the isomerization of wax is the subject of U.S. Patent 4,929,795, U. S . Patent 4,923,588, and U.S. Patent 4,937,399 respectively.
A most preferred catalyst is the subject of U.S. Patent 4, 906,601. The use of that catalyst for wax isomerization is the subject of U.S. Patent 4,923,588.
That catalyst comprises a noble Group VIII
metal on low fluoride content small particle size refractory metal oxide base. The catalyst is charac-terized by having a fluoride content in the range of 0.1 to up to but less than 2 wt%, preferably 0.1 to 1. 5 wt%, more preferably 0.2 to 1.0 wt%, a particle diame-ter of less than 1/16 inch and a preferred noble Group VIII metal loading in the range of 0.1 to 2.0 wt~. The preferred small particle æupport is 1/20 inch trilobe alumina.
As one would expect, noble metal isomeriza-tion catalysts are extremely susoeptible to deactiva-tion by the presence of heteroatom compounds (i.e. N, O
or S compound~) in the wax feed 80 care mu~t be exer-cised to remove such heteroatom materials from the wax feed charge6. When dealing with high purity waxes such as synthetic Fischer-Tropsch waxes, such precautions may not be necessary. In such cases, subjecting such waxes to very mild hydrotreating may be sufficient to insure protection for the isomerization catalyst. On the other hand, waxes obtained from natural petroleum -- 9 -- 2 ~ ~ r~ ~ r~ ~3 sources contain quantities of heteroatom compounds as well as appreciable quantities of oil which contain heteroatom compoundsO In such instances the slack waxes should be hydrotreated to reduce the level of heteroatom compounds to levels commonly accepted in the industry as tolerable for feeds to be exposed to isomerization catalysts. Such levels will typically be a N content of about 1 to 5 ppm and a S content of about 1 to 20 ppm, preferably 2 ppm or less nitrogen and 5 ppm or less sulfur. Similarly, such slack waxes prior to hydrotreating should be deoiled to an oil content in the range of 0 to 35% oil, preferably 5 to 25% oil. The hydrotreating step will employ a typical hydrotreating catalyst such as Co/Mo or Ni/Mo on alumina under standard, commercially acceptable condi-tions, e.g., temperature of 280 to 400C, space veloci-ty of 0.1 to 2.0 V/V/hr, pressure of from 500 to 3000 psig H2 and hydrogen gas rates of from 500 to 5000 SCF/bbl.
The present invention will be better under-stood by reference to the following non-limiting examples.
Figure 1 shows how the miscibility of a Fischer-Tropsch 8.7 cSt Q100C isomerate fraction boiling in the 550 to 575C range (about equivalent to a 250N viscosity grade) can be improved about 10C with the addition of 33% of a conventional 150N basestock.
Filtration studies were performed with this combined feedstock and compared with base case evaluation of the neat Fischer-Tropsch 8.7 cSt ~lOO-C wax isomerate. The isomerate was made by isomerizing a Fischer-Tropsch 150 wax as feed over an isomerization catalyst comprising 0.6 Pt/5.6% F/A12O3 at a temperature between 365 to 375C, a pressure of 1000 psig, a H2 flow rate of 7500 - lo - 2~.17~7~
SCF H2/bbl and a LHSV of 1. The dewaxing data are given in Table 1.
In an effort to reach the -21C pour target, solvent composition of the MEK/MIBK system was lowered to 10~ MEK and the dewaxing of 100% Fischer-Tropsch 8.7 cSt QlOO-C wax isomerate was performed at a filter temperature just below miscibility (degrees from miscibility -3). Typical of immiscible dewaxing, the process gave a low pour filter temperature spread and high filter rates. However, as is normally experienced with immiscible dewaxing, the wash efficiency with two liquid phases is very poor and the resulting low yield of 15.7 wt% is unacceptable. Although not measured directly it is calculated, based on typical immiscible isomerate dewaxing data that the product had a VI of about 158, a viscosity at 100C of about 8.0 cSt. It has been observed that on going from miscible dewaxing to immiscible dewaxing a viscoæity decrease is common while VI shows very little change.
Going to miscible dewaxing, as was done in the second case by raising the filtration temperature, raised the yields to acceptable levels but the attain-able pour point was raised to only -lO-C.
Using a blend of conventional 150N oil and Fischer-Tropsch 8.7 cSt ~lOO-C wax isomerate the Pilter temperature can be lowered below the target pour without immiscibility occurring. Low pours ~-21'C) were achieved at good yields. The lower filtration rate of 5.2 m3/M2d is not necessarily cause for concern as plants running 600N stocks are typically designed for filter rates of 4 to 6 m3/m2d and techniques to ; handle these rates are known.
:
.: . .
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As one might expect, the product from the dewaxer is a mixture of conventional and non-conven-tional lube. Crucial to the process is the successful separation of the light dewaxed oil from the heavy dewaxed oil e.g. the light conventional oil from the heavier isomerate oil. While any separation process (distillation, extraction, membranes, etc.) could be considered, the simplest and most straight forward process is distillation. For that reason low boiling conventional lubes are co-processed with the relatively high boiling isomerate oils. It is interesting to note that this does not imply a wide difference in viscosity grades. Due to the highly paraffinic nature of the isomerate oil it has a much higher boiling point than equivalent viscosity conventional stocks. This differ-ence in the viscosity/boiling point relationship makes the separation of a 5.0 cSt 150N oil and a 8.7 cSt Fischer Tropsch wax isomerate quite feasible as demon-strated in Table 2.
The dewaxed oil product from the co-process-ing was cut into fractions which were then reblended to roughly the same specifications as would be possessed by individually processed dewaxed oil fractions (See Table 2).
Using the 40% to Final Boiling Point blend, a 9.2 cSt, 148 VI, -22C pour product was made, leaving a 102 VI, 4.7 cSt, -22-C pour conventional stock. These specifications are very close to the parent materials.
Surprisingly it has been found that not only is the dewaxing of the heavy oil fraction made easier by the procedure of dewaxing a heavy oil/light oil blend, but also the yield of dewaxed heavy oil is higher. Thus, while 100 barrels of Fischer-Tropsch isomerate can be dewaxed to give 15.7 barrels of -21C pour oil (15.7 LV%, see Table 1), when these same 100 barrels of Fischer-Tropsch isomerates are mixed with 50 barrels of 150N oil (to give a total of 150 barrels of oil to be dewaxed) a total dewaxed oil yield of 49.3% is obtained l74 barrels DW0 based on 150 barrels mixture) and upon fractionation 60% or 44.4 barrels (60% of 74 barrels) is found to constitute the amount of oil having a VI, viscosity and pour corresponding to the 15.7 barrels obtained when the Fischer-Tropsch isomerate was dewaxed by itself. Thus, yield of the premium quality high VI
oil is increased at the same time the dewaxing is made easier (See Figure 2).
This yield increase is much greater than what one would obtain from simply mixing fractions of separately dewaxed FT isomerate and 150N oil. Linear blending of such fractions to give a final product with a ~48 VI would require a mixture of 84 LV% FT
isomerate/16 LV% 150N. This blend would produce a yield of only 18.7% compared to the about 44% of 148 VI
product obtained by co-processing. The oil product obtained by linear blending would also be of different quality. Whereas coprocessing gives a yield of 44.4%
of a 148 VI, 55.21 cSt Q 40-C, 9.19 cSt Q 100C mate-rial, linear blending would produce an 18.7% yield of a 148 VI, 44.78 cSt 0 40-C, 7.9 cSt Q lOO-C product.
Furthermore, coprocessing followed by fractionation produces a light oil of 102 VI and 5 Vis which is obviously superior to the base 150N oil fraction which, when separately dewaxed produced a DW0 of 90 VI and 5 vis .
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Claims (9)
1. A method for producing high boiling, high viscosity index dewaxed oils having a pour point of at least -21°C by solvent dewaxing under miscible condi-tions using low miscibility dewaxing solvents, said process involving the step of combining a low boiling conventional VI waxy oil with the high boiling high VI
oil and co-processing the mixture under conventional miscible solvent dewaxing conditions using the low miscibility dewaxing solvent.
oil and co-processing the mixture under conventional miscible solvent dewaxing conditions using the low miscibility dewaxing solvent.
2. The method of claim 1 wherein the high boiling, high VI oil is any natural petroleum oil hydrocracked oil, or oil obtained by the isomerization of wax, said oil having a viscosity in the range 6 to 10 cSt @100°C, a mid LV% boiling point of 450 to 550°C
and a VI of at least about 120.
and a VI of at least about 120.
3. The method of claim 1 wherein the low boiling, conventional VI waxy oil has a viscosity of about 3 to 7 cSt @100°C, a 90% off point about 0 to 300°F lower than the 10% off point of the high boiling, high VI oil and a VI of less than about 110.
4. The method of claim 1, 2 or 3 wherein the amount of low boiling, conventional VI oil added to the high boiling, high VI oil is in the range of between about 5 to 50% by volume.
5. The method of claim 4 wherein the high boiling, high VI oil has a viscosity in the range 8 to 10 cSt @100°C, a mid LV% boiling point of 475 to 525°C
and a VI of at least 140.
and a VI of at least 140.
6. The method of claim 4 wherein the low boiling conventional VI oil has a viscosity of about 4 to 6 cSt @100°C, a 90% off point about 50 to 100°F
lower than the 10% off point of the high boiling, high VI oil and a VI of less than about 100.
lower than the 10% off point of the high boiling, high VI oil and a VI of less than about 100.
7. The method of claim 5 wherein the low boiling conventional VI oil has a viscosity of about 4 to 6 cSt @100°C, a 90% off point about 50 to 100°F
lower than the 10% off point of the high boiling, high VI oil and a VI of less than about 100.
lower than the 10% off point of the high boiling, high VI oil and a VI of less than about 100.
8. The method of claim 1, 2 or 3 wherein the amount of low boiling, conventional VI oil added to the high boiling, high VI oil is in the range of about 20 to 40 vol.%.
9. The method of claim 1, 2 or 3 wherein the low miscibility dewaxing solvent is a C3-C6 ketone and mixtures thereof.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US55977990A | 1990-07-30 | 1990-07-30 | |
| US559,779 | 1990-07-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2047075A1 true CA2047075A1 (en) | 1992-01-31 |
Family
ID=24234991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2047075 Abandoned CA2047075A1 (en) | 1990-07-30 | 1991-07-15 | Low pour high vi lubes via co-processing solvent dewaxing |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP0471461B1 (en) |
| JP (1) | JPH04233996A (en) |
| CA (1) | CA2047075A1 (en) |
| DE (1) | DE69103598T2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4128381A1 (en) * | 1991-08-27 | 1993-03-04 | Mobil Oil Deutschland | CARBURETTOR FUEL ADDITIVE |
| US7655132B2 (en) * | 2004-05-04 | 2010-02-02 | Chevron U.S.A. Inc. | Process for improving the lubricating properties of base oils using isomerized petroleum product |
| SG11201400212XA (en) | 2011-09-21 | 2014-08-28 | Exxonmobil Res & Eng Co | Lubricant base oil hydroprocessing and blending |
| CN114437815B (en) * | 2020-10-30 | 2023-10-10 | 中国石油化工股份有限公司 | Method for preparing bright stock |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3365390A (en) * | 1966-08-23 | 1968-01-23 | Chevron Res | Lubricating oil production |
| DE2625635A1 (en) * | 1976-06-08 | 1977-12-22 | Texaco Development Corp | Lubricating oil with higher viscosity index - by blending hydrofined fraction with fresh oil |
-
1991
- 1991-07-15 CA CA 2047075 patent/CA2047075A1/en not_active Abandoned
- 1991-07-29 DE DE1991603598 patent/DE69103598T2/en not_active Expired - Fee Related
- 1991-07-29 EP EP19910306827 patent/EP0471461B1/en not_active Expired - Lifetime
- 1991-07-30 JP JP19029391A patent/JPH04233996A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE69103598D1 (en) | 1994-09-29 |
| EP0471461A3 (en) | 1992-03-18 |
| EP0471461B1 (en) | 1994-08-24 |
| DE69103598T2 (en) | 1994-12-22 |
| EP0471461A2 (en) | 1992-02-19 |
| JPH04233996A (en) | 1992-08-21 |
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