EP0238740B1 - Process for improving bright stock raffinate oil production - Google Patents
Process for improving bright stock raffinate oil production Download PDFInfo
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- EP0238740B1 EP0238740B1 EP19860302345 EP86302345A EP0238740B1 EP 0238740 B1 EP0238740 B1 EP 0238740B1 EP 19860302345 EP19860302345 EP 19860302345 EP 86302345 A EP86302345 A EP 86302345A EP 0238740 B1 EP0238740 B1 EP 0238740B1
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- European Patent Office
- Prior art keywords
- oil
- raffinate
- solvent
- extract
- bright stock
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- 238000000034 method Methods 0.000 title claims description 17
- 238000004519 manufacturing process Methods 0.000 title description 13
- 239000003921 oil Substances 0.000 claims description 92
- 239000002904 solvent Substances 0.000 claims description 35
- 239000010687 lubricating oil Substances 0.000 claims description 21
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 20
- 229930195733 hydrocarbon Natural products 0.000 claims description 15
- 239000004215 Carbon black (E152) Substances 0.000 claims description 14
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 14
- 150000002430 hydrocarbons Chemical class 0.000 claims description 11
- 239000001294 propane Substances 0.000 claims description 10
- 238000004064 recycling Methods 0.000 claims description 7
- -1 alkane hydrocarbon Chemical class 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 239000003849 aromatic solvent Substances 0.000 claims description 4
- 238000000638 solvent extraction Methods 0.000 claims description 4
- 230000001747 exhibiting effect Effects 0.000 claims 1
- 238000000605 extraction Methods 0.000 description 24
- 239000007788 liquid Substances 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 238000005292 vacuum distillation Methods 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000002199 base oil Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000011143 downstream manufacturing Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000012208 gear oil Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000010721 machine oil Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
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Classifications
-
- 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
- C10G53/00—Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes
- C10G53/02—Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes plural serial stages only
- C10G53/04—Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes plural serial stages only including at least one extraction step
- C10G53/06—Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes plural serial stages only including at least one extraction step including only extraction steps, e.g. deasphalting by solvent treatment followed by extraction of aromatics
Definitions
- the present invention relates to lube oil manufacture and more specifically, is directed to increased production of Bright Stock raffinate oil.
- Bright Stock raffinate oil is a high-boiling hydrocarbon fraction produced during lube oil manufacture and is well-known in the art.
- a vacuum residuum suitable for lube oil production has been deasphalted by contacting and extracting with a propane solvent
- the propane solvent is stripped off and the resulting extract oil is extracted with an aromatic solvent, such as N-methylpyrrolidone (NMP), to remove aromatic hydrocarbons.
- NMP N-methylpyrrolidone
- the resulting extracted, deasphalted oil phase containing mainly saturated hydrocarbons, is known in the trade as "Bright Stock raffinate oil”.
- This raffinate is subsequently contacted with extracting agents like ketones or alkane hydrocarbon solvents to remove waxy hydrocarbons which are detrimental to lube oil viscosity properties and then subjected to HYDROFINING TM to improve the appearance of the oil and remove sulfur.
- extracting agents like ketones or alkane hydrocarbon solvents to remove waxy hydrocarbons which are detrimental to lube oil viscosity properties and then subjected to HYDROFINING TM to improve the appearance of the oil and remove sulfur.
- the resulting oil is termed "Bright Stock Oil” and is a lubes base stock component from which many lubricating oils, e.g., gear oil, machine oil, automobile engine oil, are made by blending with other lube stock components.
- a current practice in the industry following NMP extraction of deasphalted oil in a lubes process, is to strip off the NMP from the extracted phase and send the residual extract oil, containing mostly aromatics and some dissolved recoverable Bright Stock raffinate oil, to a different process involving a catalytic cracker unit for processing to produce fuel oils.
- Such practice results in a yield debit for Bright Stock raffinate oil in the lube oil process and ultimately the Bright Stock base oil yield. This step is performed primarily because it is believed that recycling said extract oil again through the extraction step would result in a very low recovery of recoverable raffinate which may not be justified in light of the attendant recycling cost and process time required.
- a hydrocarbon feedstock such as a reduced crude, suitable for lube oil production, enters the vacuum distillation zone 10 through line 12. Distillate is shown being withdrawn from zone 10 through lines 14, 16 and 18. Vacuum residuum from zone 10 suitable for lube oil production passes through line 20 and is mixed with an aromatic extract oil (line 40) in line 22 and passed into a first extraction zone, being deasphalting zone 24.
- the feed to zone 24 countercurrently contacts a low molecular weight hydrocarbon solvent such as propane, which enters through a line 26, producing a deasphalted lube oil (DAO) solution exiting through line 28 and an asphaltic residue exiting through line 30.
- DAO deasphalted lube oil
- the deasphalted oil after propane stripoff enters a second extraction zone 32, through line 28, where it is countercurrently contacted with an aromatics solvent (for extracting aromatics including benzene, toluene and xylene) such as N-methylpyrrolidone (NMP) or phenol, which enters through upper line 34.
- aromatics solvent for extracting aromatics including benzene, toluene and xylene
- NMP N-methylpyrrolidone
- phenol phenol
- this portion of the extract oil is then passed through line 40 and admixed with the vacuum residuum feed entering from line 20 in the amount of 10-20 LV%, based on said residuum, in line 22 to the deasphalter.
- the added extract oil increases the total LV% of deasphalter feed to the deasphalter.
- the remainder of the extract oil in line 38 is passed to a cat cracker unit or other suitable disposition through line 42.
- the obtained Bright Stock raffinate oil via recycle in line 36 is present in a substantially greater amount based on the same amount of starting vacuum residuum, as deasphalter feed, as compared to that obtained from vacuum residuum not admixed with recycled extract oil in the base case.
- the yield of Bright Stock raffinate oil obtained from vacuum residuum is generally in the range of about 3.3 LV%, based on the residuum.
- Use of extract oil recycle according to the present invention significantly increases the amount of recoverable Bright Stock raffinate oil to values above 3.5 LV%.
- Distillation zone 10 typically comprises a vacuum distillation zone, or vacuum pipestill.
- Distillation zone 10 commonly is a packed or a trayed column.
- the bottoms temperature of zone 10 typically is maintained within the range of about 350 ° to about 450 ° C, while the bottoms pressure is maintained within the range of 5 to about 15 cm Hg.
- the specific conditions employed will be a function of several variables, including the feed utilized, the distillate specifications, and the relative amounts of distillate and bottoms desired.
- the resulting vacuum residuum obtained comprises between about 10 and about 50 weight percent of the total residuum feed in line 12, and has a boiling point (1 atm.) above about 370 ° C.
- Deasphalting zone 24 typically will comprise a contacting zone, preferably a countercurrent contacting zone, in which the hydrocarbon feed entering through line 22 is contacted with a solvent, such as a liquid light alkane hydrocarbon.
- Deasphalting zone 24 preferably includes internals adapted to promote intimate liquid-liquid contacting, such as sieve trays or shed row contactors.
- the extract stream comprising deasphalted oil and a major portion of the solvent, exits the deasphalting zone 24 for further separation of the deasphalted oil from the solvent, with the solvent fraction recirculated via line 40 to deasphalting zone 24 for reuse.
- the preferred solvents generally used for deasphalting include C 2 -Ca alkanes, i.e., ethane, propane, butane, pentane, hexane, heptane and octane, with the most preferred being propane for lube oil processing.
- the operating conditions for deasphalting zone 24 are dependent, in part, upon the solvent utilized, the characteristics of the hydrocarbon feedstock, and the physical properties of the deasphalted oil or asphalt desired.
- the solvent treat typically will range between about 200 liquid-volume percent (LV%) and about 1000 LV% of the residuum feed added to deasphalting zone 24.
- Extraction zone 32 typically comprises a contacting zone, preferably a countercurrent contact zone, in which the hydrocarbon feed entering through line 28 is contacted with an aromatic solvent, such as N-methylpyrrolidone (NMP) furfural or phenol.
- Extraction zone 32 preferably has internals designed to promote intimate liquid-liquid contact.
- the raffinate stream comprising a major portion of the saturates and a small portion of the extraction solvent, exits the extraction zone through line 36 for further separation of the raffinate from the solvent fraction, with the solvent fraction recirculated to extraction zone 32 for reuse.
- the extract stream comprising a major proportion of the aromatics and a major portion of the extraction solvent, exits the extraction zone through line 38 for further separation of the aromatics from the solvent fraction, with the solvent fraction recirculated to extraction zone 32 for reuse.
- the operating conditions for extraction zone 32 are dependent in part, upon the solvent utilized, the characteristics of the hydrocarbon feedstock, and the physical properties of the raffinate oil desired.
- the solvent treat will typically range from 100 to 400 LV% of the DAO feed to the extraction zone 32 and contain from 0.5 to 6.0 LV% water.
- Arabian Light Vacuum Resid (residuum) from a vacuum distillation zone and an extract oil derived from an Arabian Light DAO (deasphalted oil) were the deasphalter feed materials utilized during a deasphalting process with propane solvent. Typical properties of the two materials are summarized below in Table 1.
- the extract oil was mixed with the vacuum residuum in a 10-20 LV% based on the residuum, which was in addition to the amount of residuum normally used resulting in a greater LV% of total feed mixture.
- the values in (a) for DAO yield are based on the total vacuum residuum/extract oil deasphalter feed; the values in (b) for raffinate yield are based on the DAO to the extraction unit and the values in (c) for increased raffinate yield, being Bright Stock basestock oil, as a result of the recycle, are based on the total vacuum residuum/extract oil deasphalter feed.
- the deasphalter feedstock mixture was contacted with propane solvent in the deasphalter in a standard procedure.
- the DAO was then extracted with NMP to Bright Stock quality specifications and the appropriate LV% extract oil, after NMP strip off, recycled to the deasphalter and the process repeated.
- the yields for the deasphalting, extraction and overall Bright Stock base oil (raffinate) have been presented graphically in Figures 2(a-c) as a function of added LV% Extract Oil recycle. As seen in Figure 2(a), the DAO yield increases with increasing Extract Oil recycle while the LV% Raffinate yield in (b) based on total extraction yield decreases.
- Example 2 Utilizing the apparatus and general procedure described above in Example 1, a comparative run was made using no recycle versus one using 15 LV% extract oil in the deasphalter/extraction steps.
- the base case run is indicated by numeral 1) and the recycle case as 2).
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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)
Description
- The present invention relates to lube oil manufacture and more specifically, is directed to increased production of Bright Stock raffinate oil.
- Bright Stock raffinate oil is a high-boiling hydrocarbon fraction produced during lube oil manufacture and is well-known in the art. Generally, in the art, after a vacuum residuum suitable for lube oil production has been deasphalted by contacting and extracting with a propane solvent, the propane solvent is stripped off and the resulting extract oil is extracted with an aromatic solvent, such as N-methylpyrrolidone (NMP), to remove aromatic hydrocarbons. The resulting extracted, deasphalted oil phase, containing mainly saturated hydrocarbons, is known in the trade as "Bright Stock raffinate oil". This raffinate is subsequently contacted with extracting agents like ketones or alkane hydrocarbon solvents to remove waxy hydrocarbons which are detrimental to lube oil viscosity properties and then subjected to HYDROFININGTM to improve the appearance of the oil and remove sulfur. The resulting oil is termed "Bright Stock Oil" and is a lubes base stock component from which many lubricating oils, e.g., gear oil, machine oil, automobile engine oil, are made by blending with other lube stock components.
- A current practice in the industry, following NMP extraction of deasphalted oil in a lubes process, is to strip off the NMP from the extracted phase and send the residual extract oil, containing mostly aromatics and some dissolved recoverable Bright Stock raffinate oil, to a different process involving a catalytic cracker unit for processing to produce fuel oils. Such practice results in a yield debit for Bright Stock raffinate oil in the lube oil process and ultimately the Bright Stock base oil yield. This step is performed primarily because it is believed that recycling said extract oil again through the extraction step would result in a very low recovery of recoverable raffinate which may not be justified in light of the attendant recycling cost and process time required.
- An example of the prior art in the area is U.S. Patent No. 2,570,044 which discloses recycling of an aromatic extract oil stream derived from a deasphalted oil to a deasphalter feed during lubes production. This is disclosed as being carried out in order to eliminate the formation of a third phase which tends to foul the deasphalter internals.
- In addition, the patent claims that the overall yield of high Viscosity Index (VI) components is increased relative to a conventional scheme without extract oil recycle. The aforementioned patent also teaches that the quantity of extract oil recycled to prevent asphaltic deposition is from 3 to 25 percent by volume (LV%) based on the reduced crude oil charged to the deasphalting treater tower. Furthermore, it is stated that recycling larger amounts (greater than 25 LV%) of extract oil is not disadvantageous but actually increases the yields of high Viscosity Index (VI) oil.
- It has been found, in direct contrast to the teaching of the above-identified patent, that for the production of lubes Bright Stock raffinate oil within specifications, there is a distinct range for extract oil recycle being from 10 to 20 LV% based on the total reduced crude feed to the deasphalter. Adding extract oil in excess of 20 LV%, results in a dewaxed raffinate oil Conradson Carbon Residue (CCR) exceeding the equivalent of 1.0 weight percent. This leads to unacceptable Bright Stock Conradson Carbon Residue values exceeding the required specification of <0.7 wt.% with conventional downstream processing. Values of CCR exceeding specification arise due to the high CCR content of Bright Stock extract oil. In addition, it has been found that a substantial deasphalting yield credit results with extract oil recycle accompanied by an extraction yield debit. As a result of the operation of these two features, the maximum yield of high VI oil occurs between 10 and 20 LV% extract oil recycle and adding in excess of 20 LV% actually causes the overall yield to begin to decrease. The subject process is particularly useful in refinery operations being conducted under crude-limited conditions.
- In accordance with this invention there is provided a process for increasing the amount of Bright Stock raffinate oil derived from the solvent extraction of deasphalted lube oil, involving the steps of:
- (a) extracting a vacuum residuum with a low molecular weight alkane hydrocarbon solvent resulting in a deasphalted lube oil and asphaltic residue;
- (b) separating said deasphalted lube oil and said residue;
- (c) separating said hydrocarbon solvent from said deasphalted lube oil;
- (d) extracting said deasphalted lube oil obtained from step (c) with an aromatic solvent resulting in a Bright Stock raffinate oil solution and an extract oil solution, said extract oil solution comprised of dissolved aromatics and recoverable raffinate;
- (e) separating said raffinate oil solution from said extract oil solution obtained from step (d); and
- (f) separating said aromatics solvent from said extract oil solution obtained from step (e); in which said improvement comprises the steps of: (g) recycling said extract oil, from which the aromatics solvent has been removed, obtained from step
- (f), to step (a) and combining said extract oil with said vacuum residuum, in a 10-20 LV%, based on said residuum, prior to said deasphalting;
- (h) repeating step (a);
- (i) repeating step (b);
- Q) repeating step (c);
- (k) extracting said deasphalted oil obtained from step (1) with said aromatics solvent resulting in said Bright Stock raffinate oil and said extract oil, wherein said obtained raffinate is present in a substantially greater amount, based on said vacuum residuum, as compared to said raffinate obtained in step (d).
-
- Figure 1 is a simplified flow diagram illustrating apparatus and connections of one embodiment for practicing the subject invention.
- Figure 2 illustrates three different plots obtained by practice of the subject invention showing the variation, as a function of extract oil recycle in LV%; of:
- (a) the deasphalted oil (DAO) yield based on total deasphalter feed;
- (b) raffinate yield based on total extraction unit feed; and
- (c) raffinate yield based on total deasphalter unit feed.
- Figure 3 is a process schematic diagram showing the increased raffinate yield in using extract oil recycle vs. the base case (no recycle).
- An understanding of the improved process of the invention and details for carrying it out can readily be obtained by referring to Figure 1.
- In Figure 1, a hydrocarbon feedstock such as a reduced crude, suitable for lube oil production, enters the
vacuum distillation zone 10 throughline 12. Distillate is shown being withdrawn fromzone 10 throughlines zone 10 suitable for lube oil production passes throughline 20 and is mixed with an aromatic extract oil (line 40) inline 22 and passed into a first extraction zone, being deasphaltingzone 24. The feed to zone 24 countercurrently contacts a low molecular weight hydrocarbon solvent such as propane, which enters through aline 26, producing a deasphalted lube oil (DAO) solution exiting throughline 28 and an asphaltic residue exiting throughline 30. The deasphalted oil after propane stripoff enters asecond extraction zone 32, throughline 28, where it is countercurrently contacted with an aromatics solvent (for extracting aromatics including benzene, toluene and xylene) such as N-methylpyrrolidone (NMP) or phenol, which enters throughupper line 34. A saturates-rich Bright Stock oil raffinate solution passes out ofzone 32 throughupper line 36 and the extract oil solution, comprised of dissolved extracted aromatics and recoverable raffinate passes out throughlower line 38. After separation of the extraction solvent NMP from a portion of the extract oil solution, this portion of the extract oil is then passed throughline 40 and admixed with the vacuum residuum feed entering fromline 20 in the amount of 10-20 LV%, based on said residuum, inline 22 to the deasphalter. The added extract oil increases the total LV% of deasphalter feed to the deasphalter. The remainder of the extract oil inline 38 is passed to a cat cracker unit or other suitable disposition throughline 42. The obtained Bright Stock raffinate oil via recycle inline 36 is present in a substantially greater amount based on the same amount of starting vacuum residuum, as deasphalter feed, as compared to that obtained from vacuum residuum not admixed with recycled extract oil in the base case. - The yield of Bright Stock raffinate oil obtained from vacuum residuum is generally in the range of about 3.3 LV%, based on the residuum. Use of extract oil recycle according to the present invention, significantly increases the amount of recoverable Bright Stock raffinate oil to values above 3.5 LV%.
-
Distillation zone 10 typically comprises a vacuum distillation zone, or vacuum pipestill.Distillation zone 10 commonly is a packed or a trayed column. The bottoms temperature ofzone 10 typically is maintained within the range of about 350° to about 450°C, while the bottoms pressure is maintained within the range of 5 to about 15 cm Hg. The specific conditions employed will be a function of several variables, including the feed utilized, the distillate specifications, and the relative amounts of distillate and bottoms desired. Typically, the resulting vacuum residuum obtained comprises between about 10 and about 50 weight percent of the total residuum feed inline 12, and has a boiling point (1 atm.) above about 370°C. - The operation of deasphalting zones is well known by those skilled in the art.
Deasphalting zone 24 typically will comprise a contacting zone, preferably a countercurrent contacting zone, in which the hydrocarbon feed entering throughline 22 is contacted with a solvent, such as a liquid light alkane hydrocarbon.Deasphalting zone 24 preferably includes internals adapted to promote intimate liquid-liquid contacting, such as sieve trays or shed row contactors. The extract stream, comprising deasphalted oil and a major portion of the solvent, exits thedeasphalting zone 24 for further separation of the deasphalted oil from the solvent, with the solvent fraction recirculated vialine 40 to deasphaltingzone 24 for reuse. The preferred solvents generally used for deasphalting include C2-Ca alkanes, i.e., ethane, propane, butane, pentane, hexane, heptane and octane, with the most preferred being propane for lube oil processing. The operating conditions fordeasphalting zone 24 are dependent, in part, upon the solvent utilized, the characteristics of the hydrocarbon feedstock, and the physical properties of the deasphalted oil or asphalt desired. The solvent treat typically will range between about 200 liquid-volume percent (LV%) and about 1000 LV% of the residuum feed added todeasphalting zone 24. A discussion of deasphalting operation is presented in Advances in Petroleum Chemistry and Refining, Volume 5, pages 284-291, John Wiley and Sons, New York, New York (1962), the disclosure of which is incorporated by reference. - The operation of lube oil extraction zones is well known to those skilled in the art.
Extraction zone 32 typically comprises a contacting zone, preferably a countercurrent contact zone, in which the hydrocarbon feed entering throughline 28 is contacted with an aromatic solvent, such as N-methylpyrrolidone (NMP) furfural or phenol.Extraction zone 32 preferably has internals designed to promote intimate liquid-liquid contact. The raffinate stream comprising a major portion of the saturates and a small portion of the extraction solvent, exits the extraction zone throughline 36 for further separation of the raffinate from the solvent fraction, with the solvent fraction recirculated toextraction zone 32 for reuse. The extract stream, comprising a major proportion of the aromatics and a major portion of the extraction solvent, exits the extraction zone throughline 38 for further separation of the aromatics from the solvent fraction, with the solvent fraction recirculated toextraction zone 32 for reuse. The operating conditions forextraction zone 32 are dependent in part, upon the solvent utilized, the characteristics of the hydrocarbon feedstock, and the physical properties of the raffinate oil desired. The solvent treat will typically range from 100 to 400 LV% of the DAO feed to theextraction zone 32 and contain from 0.5 to 6.0 LV% water. - To illustrate the present invention, Arabian Light Vacuum Resid (residuum) from a vacuum distillation zone and an extract oil derived from an Arabian Light DAO (deasphalted oil) were the deasphalter feed materials utilized during a deasphalting process with propane solvent. Typical properties of the two materials are summarized below in Table 1.
- The increase in Arabian Light Bright Stock oil production was demonstrated by admixing in the Figure 2 listed LV% proportions, the above-described Arabian Light extract oil stream (40), being the extract from the solvent extraction of an Arabian Light deasphalted oil, with the above-described Arabian Light Vacuum Residuum as a deasphalter feed.
- The extract oil was mixed with the vacuum residuum in a 10-20 LV% based on the residuum, which was in addition to the amount of residuum normally used resulting in a greater LV% of total feed mixture. In Figure 2, the values in (a) for DAO yield are based on the total vacuum residuum/extract oil deasphalter feed; the values in (b) for raffinate yield are based on the DAO to the extraction unit and the values in (c) for increased raffinate yield, being Bright Stock basestock oil, as a result of the recycle, are based on the total vacuum residuum/extract oil deasphalter feed.
- The deasphalter feedstock mixture was contacted with propane solvent in the deasphalter in a standard procedure. The DAO was then extracted with NMP to Bright Stock quality specifications and the appropriate LV% extract oil, after NMP strip off, recycled to the deasphalter and the process repeated. The yields for the deasphalting, extraction and overall Bright Stock base oil (raffinate) have been presented graphically in Figures 2(a-c) as a function of added LV% Extract Oil recycle. As seen in Figure 2(a), the DAO yield increases with increasing Extract Oil recycle while the LV% Raffinate yield in (b) based on total extraction yield decreases. The combination of these effects results in a maximum increase in Raffinate yield, i.e., Bright Stock production as seen in Figure 2(e) in the 10-20 LV% range, and particularly at 15 LV% Extract Oil recycle. Recycle at levels below 10 LV% results in sharply reduced Bright Stock yields, and recycle levels above 20 LV%, renders it difficult to maintain the Bright Stock Conradson Carbon Residue (CCR) quality specification.
-
- Conventional downstream processing (HYDROfining) reduces the dewaxed raffinate oil CCR by 0.3 wt.% which brings the 20 LV% recycle case down to 0.7 wt.% which is equivalent to the Bright Stock CCR specification. Recycling more than 20 LV% extract oil makes it very difficult to meet the Bright Stock CCR specification and is unacceptable in a conventional refinery operation.
- Utilizing the apparatus and general procedure described above in Example 1, a comparative run was made using no recycle versus one using 15 LV% extract oil in the deasphalter/extraction steps. The base case run is indicated by numeral 1) and the recycle case as 2).
- As seen from the results depicted in the flow diagram of Figure 3, starting with 1.0 liquid volume (LV) of vacuum residuum in the base case led to a 34% production of deasphalted oil (DAO), after propane extraction. Subsequent NMP solvent extraction produced 72% yield of raffinate based on the DAO resulting in 0.245 LV raffinate based on starting vacuum residuum as deasphalter feed.
- By contrast, starting with 1.0 LV of vacuum resid, together with 0.175 LV of extract oil, representing a 15 LV% recycle, led to a 41% yield of DAO after deasphalting. Subsequent NMP extraction produced 55% yield of raffinate based on the DAO resulting in 0.265 LV raffinate. This represents an 8.2% increase in production of raffinate based on starting vacuum resid as compared to the base case involving no recycle.
Claims (5)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/648,013 US4592832A (en) | 1984-09-06 | 1984-09-06 | Process for increasing Bright Stock raffinate oil production |
EP19860302345 EP0238740B1 (en) | 1986-03-27 | 1986-03-27 | Process for improving bright stock raffinate oil production |
SG74289A SG74289G (en) | 1986-03-27 | 1989-11-16 | Process for improving bright stock raffinate oil production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP19860302345 EP0238740B1 (en) | 1986-03-27 | 1986-03-27 | Process for improving bright stock raffinate oil production |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0238740A1 EP0238740A1 (en) | 1987-09-30 |
EP0238740B1 true EP0238740B1 (en) | 1989-09-06 |
Family
ID=8195949
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19860302345 Expired EP0238740B1 (en) | 1984-09-06 | 1986-03-27 | Process for improving bright stock raffinate oil production |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0238740B1 (en) |
SG (1) | SG74289G (en) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2570044A (en) * | 1948-12-23 | 1951-10-02 | Phillips Petroleum Co | Propane fractionation of reduced crude oil with recycle of a solvent extract |
FR1060165A (en) * | 1951-07-03 | 1954-03-31 | Edeleanu Gmbh | Process for preparing high viscosity oils |
BE559418A (en) * | 1957-07-16 |
-
1986
- 1986-03-27 EP EP19860302345 patent/EP0238740B1/en not_active Expired
-
1989
- 1989-11-16 SG SG74289A patent/SG74289G/en unknown
Also Published As
Publication number | Publication date |
---|---|
SG74289G (en) | 1990-04-20 |
EP0238740A1 (en) | 1987-09-30 |
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