US3016350A - Hydrofining lubricating oil - Google Patents
Hydrofining lubricating oil Download PDFInfo
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- US3016350A US3016350A US741346A US74134658A US3016350A US 3016350 A US3016350 A US 3016350A US 741346 A US741346 A US 741346A US 74134658 A US74134658 A US 74134658A US 3016350 A US3016350 A US 3016350A
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- hydrofining
- lubricating oil
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- 239000010687 lubricating oil Substances 0.000 title claims description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 24
- 239000003054 catalyst Substances 0.000 claims description 20
- 230000008569 process Effects 0.000 claims description 20
- 239000001257 hydrogen Substances 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 15
- 229910052717 sulfur Inorganic materials 0.000 claims description 15
- 239000011593 sulfur Substances 0.000 claims description 15
- 239000003921 oil Substances 0.000 claims description 11
- 238000009835 boiling Methods 0.000 claims description 8
- 239000003208 petroleum Substances 0.000 claims description 6
- 230000006872 improvement Effects 0.000 description 11
- 239000000047 product Substances 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 239000003112 inhibitor Substances 0.000 description 5
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910000428 cobalt oxide Inorganic materials 0.000 description 2
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- KYYSIVCCYWZZLR-UHFFFAOYSA-N cobalt(2+);dioxido(dioxo)molybdenum Chemical compound [Co+2].[O-][Mo]([O-])(=O)=O KYYSIVCCYWZZLR-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
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
- C10G49/00—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00
- C10G49/007—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 in the presence of hydrogen from a special source or of a special composition or having been purified by a special treatment
-
- 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
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/10—Lubricating oil
Definitions
- the present invention is concerned with a process for the hydrofining of hydrocarbons boiling in the lubricating oil boiling range.
- the invention is more particularly concerned with an improved hydrofining process for upgrading and improving the color of petroleum lubricating oils.
- f Hydrofining is a catalytic hydrogen-treating process to improve the quality of a wide range of petroleum stock. The process is primarily used to improve odor, appearance, color, stability, combustion characteristics and other quality factors unique to a given product. Hydrofining is especially important since it minimizes fluctuation in product quality due to, changes in crude source and achieves this with 100% yield of liquid product.
- sulfur acts as a natural inhibitor and is therefore beneficial in lubricating oils used under conditions which favor oxidative reactions.
- various oxygenated materials are formed which may be acidic in nature and act as'further oxidation catalysts or attack alloy. bearings, form polymeric materials which plate out on hot engine parts; or act as a binder in holding together sludge which impairs piston ring performance and plugs oil lines and filters.
- a dewaxed feed oil consisting of hydrocarbon fractions boiling in the lubricating oil boiling range (about 700 F. to 1100 F., at 760 mm. pressure) is introduced into furnace zone 3 by means of feed line 2.
- the lub-ricating oil is heated to a temperature of from -4505S0 F.
- this heated lubricating oil fraction is withdrawn from zone 3 into feed l-ine 4 and introduced into hydrofining reactor zone 6.
- zone 6 Simultaneously' with the introduction of lubricating oil feed into Zone 6, hydrogen is introduced into zone 6 bymeans of line 12 and water is introduced into 'zone' 6'by means of line 5.
- the temperature, pressure, and 'other' operating conditions in zone 6, which will be hereinafter described, are adjusted to secure a hydro fining operation.
- the hydrofin'edproduct is withdrawn from zone 6 by means of line 7, passed through a cooling zone 8 and then introduced into a hydrogen separation zone 9. Hydrogen is removed overhead from separation zone 9 by means of line 10, recompressed in compressor zone 11 and then preferably recycled to zone 6 via'line 12. Fresh hydrogen is added to recycle hydrogen line 12 by means of line 13 and introduced into reactor 6 with the recycle hydrogen.
- the hydrofined product, free of hydrogen, is removed from the bottom of zone 9 by means of line 14 and introduced into steam stripper 15. Steam is introduced into stripper 15 by means of line 18 and temperature and pressure-are adapted to effect the removal of hydrogen sulfide and any light or low boiling hydrocarbons by means of line 16. A hydrofined lubricating oil product having a satisfactory color is withdrawn from zone 15 by means of line'17;
- HYDROFINING CONDITIONS Preferred Range Temperature, F 500 450-550. Pressure. p.s.i.g 400 250-1500. Feed ate, v lhr lv 1.0 0.2-4.0. H feed, s.e.f./b 500 10-1000. H2 consumption, s.c.f./b less than 100. Water, lbs/b 2 .25-20.
- phorus or zine compounds to the lubricating oil. These compounds are used in amounts of from 0.1% or less up to 4 Wt. percent.
- a process which would; improve color and protect the natural inhibitors would reduce or elimimate the need for these added inhibitors and therefore be a marked improvement in the art.
- a The object of this invention is to provide the-art with an improved hydrofining process for the improvement of color of lubricating oil. It is also the object of this invention to provide a method of improving the color of lubricating oil without the removal of sulfur.
- either water introduction may be accomplished in several different manners. Either water or steam may be added separately as shown in the drawing o'rfeither may be added 'to the lubricating oil before the oil enters the reactor zone. If steam is used it may be added to the hydrogen before the hydrogen enters the reactor zone.
- water in the present invention it is preferred to use distilled water, although ordinary undistilled water'ean be employed. If steam is used, it need only be at sufficient pressure to enter the system.
- the quantity of water used in the present invention may vary from .25 to 20 pounds of water per barrel of oil, although the preferred amount is about 2 pounds of water per barrel of lubricating oil feed.
- the exact explanation of why the addition of thewater improves the lubricating oil color is. not known. It appears that the water has the effect of making the catalyst more active. Accordingly, a very small quantity'ofwater is operable and the addition of large quantities of water do not seem to interfere with the improvement in color.
- the quantity of water added may be based on the volume percent of water vapor in the hydrogen atmosphere during hydrofining.
- the quantity of water vapor in the hydrogen atmosphere is in the range of about 5 to 50 volume percent.
- the preferred amount is about 40 volume percent.
- 40 volume percent of water in the hydrogen atmosphere would correspond to a water content of approximately 2 to 20 pounds of water per barrel of lubricating oil feed.
- the amount of water shown in the examples which follow is approximately 40 volume percent or 2.2 pounds of water per barrel of lubricating oil feed.
- the catalyst utilized in the present process may comprise known hydrofining catalysts. While the preferred catalyst of the present invention comprises cobalt molyb, date on alumina, or molybdenum sulfide on alumina, the use of a specific hydrofining catalyst is not required or considered essential to the invention. In the preferred cobalt molybdate catalyst, the amount of cobalt oxide is about 1% to 4% and of molybdenumoxide about 12% to 16% based on the weight of the catalyst.
- the molybdenum sulfide on alumina catalyst may consist of about to molybdenum sulfide based on the weight of the catalyst.
- the catalyst may be prepared by any known methods.
- Regeneration of the catalyst may be required periodically depending largely. upon the nature of the feed stock. This regeneration is conveniently carried out at a temperature of about 900 F. with an oxygen containing gas.
- Example I A dewaxed, non-extracted light lubricating oil distillate from Leduc type crude having the following inspections:
- the color of the lube oil product is. materially improved by the addition of. water when hydrofining at a temperature of 500 F.
- Example II In this example, the same type feed and hydrofining conditions as were used in Example I were employed.
- the catalyst used was 131 grams of a catalyst consisting of 14 wt. percent molybdenum oxide, 2.5 wt. percent cobalt oxide and 83.5 wt. percent gamma alumina. 800 cc.
- Example II Water added to each charge Tag Pobinson Color Wt. percent 5 Run No. Sulfur
- the data of Example II clearly show that a marked improvement in lubricating oil color is obtained by the use of water in accord with this invention. Also, the data show that even though a color improvement is obtained at a temperature of 500 F. when using water, it. is ac-v complished with little or no removal of sulfur.
- Example Ill The lubricating oil feed, catalyst, and hydrofining conditions employed in runs 713 and 714 are the same as those used in Example II, with the exception of the hydrofining temperature, which is noted below. Runs 813 to 816 are repeatedfrom Example II.
- runs No. 713 and No. 714 show that although improvement in color can be obtained. by hydrofining at a temperature of 600 F.,- the use of this relatively high temperature necessarily results in sulfur removal.
- the information obtained from runs No. 813 and No. 814 shows that hydrofining at 500 F. does not remove sulfur, but little color improvement is obtained.
- Runs No. 815 and No. 816 were made by hydrofining at a temperature of 500 F. using water in ace cord with the present invention and color improvement was obtained without sulfur removal.
- a process for upgrading and improving the color of a petroleum lubricating oil which'comprises hydrofining a lubricating oil feed boiling in the range of about 700 F. to 1100 F. at 760 mm. pressure at a temperature of about 450 to 550 F. and pressure of from about 250 to 1500 p.s.i.g'., in contact with a hydrofining catalyst and in the presence of a hydrogen atmosphere containing from about 5 to volume percent of water vapor thereby improving the color of the oil without removing an appreciable quantity of sulfur.
- a process for upgrading and improving the color of petroleum lubricating oil which comprises hydrofining a lubricating oil feed boiling in the range of about 700 F. to 1100 F. at 760 mm. pressure at a temperature of about 450 to 550 F. and pressure of from about 250 to 1500 p.s.i.g., in contact with a hydrofining catalyst and in the presence of added water in quantities ranging from about 0.25 to 20 pounds of water per barrel of lubricating oil feed thereby improving the color of the oil without removing an appreciable quantity of sulfur.
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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
United States PatentQ1 3,016,350 HYDROFINING LUBRICATiNG OIL Roger M. Butler and Robert Kartzmark, Sarnia, Ontario, Canada, assignors to Esso Research and Engineering Company, a corporation of Delaware Filed June 11, 1958, Ser. No. 741,346
8 Claims. (Cl. 208-264) The present invention is concerned with a process for the hydrofining of hydrocarbons boiling in the lubricating oil boiling range. The invention is more particularly concerned with an improved hydrofining process for upgrading and improving the color of petroleum lubricating oils. f Hydrofining is a catalytic hydrogen-treating process to improve the quality of a wide range of petroleum stock. The process is primarily used to improve odor, appearance, color, stability, combustion characteristics and other quality factors unique to a given product. Hydrofining is especially important since it minimizes fluctuation in product quality due to, changes in crude source and achieves this with 100% yield of liquid product.
An unique use of hydrofining is its application to lubricating oils. This process has been successfully applied to most all types of lubricating oil and has been found to possess many advantages over previous lube oil treating techniques. Not only is it possible to control lube quality from varying crude sources but equipment is relatively simple, operation is continuous, and there is no major waste disposal problem.
Prior to the present invention, it was generally believed that it was impossible to obtain an improvement in lubricating oil color without hydrofining at'the relatively high temperature of about 600 F. By hydrofining at this relatively high temperature,-it is impossible to deeolorize the lubricating oil without removing an appreciable quantity of sulfur. 4
l Although the removal or reduction of sulfur content from some lubricating oils is required or advantageous, it is equally true that sulfur acts as a natural inhibitor and is therefore beneficial in lubricating oils used under conditions which favor oxidative reactions. Under these conditions, various oxygenated materials are formed which may be acidic in nature and act as'further oxidation catalysts or attack alloy. bearings, form polymeric materials which plate out on hot engine parts; or act as a binder in holding together sludge which impairs piston ring performance and plugs oil lines and filters.
To improve resistance against oxidative degradation, it is common to add certain inhibitors suehas sulfur, phos- T ee ing illustrating diagrammatically a flow plan of one embodiment of the same. Referring specifically to the drawing, a dewaxed feed oil consisting of hydrocarbon fractions boiling in the lubricating oil boiling range (about 700 F. to 1100 F., at 760 mm. pressure) is introduced into furnace zone 3 by means of feed line 2. The lub-ricating oil is heated to a temperature of from -4505S0 F. In accordance with the present invention,- this heated lubricating oil fraction is withdrawn from zone 3 into feed l-ine 4 and introduced into hydrofining reactor zone 6. Simultaneously' with the introduction of lubricating oil feed into Zone 6, hydrogen is introduced into zone 6 bymeans of line 12 and water is introduced into 'zone' 6'by means of line 5. The temperature, pressure, and 'other' operating conditions in zone 6, which will be hereinafter described, are adjusted to secure a hydro fining operation. i
The hydrofin'edproduct is withdrawn from zone 6 by means of line 7, passed through a cooling zone 8 and then introduced into a hydrogen separation zone 9. Hydrogen is removed overhead from separation zone 9 by means of line 10, recompressed in compressor zone 11 and then preferably recycled to zone 6 via'line 12. Fresh hydrogen is added to recycle hydrogen line 12 by means of line 13 and introduced into reactor 6 with the recycle hydrogen.
The hydrofined product, free of hydrogen, is removed from the bottom of zone 9 by means of line 14 and introduced into steam stripper 15. Steam is introduced into stripper 15 by means of line 18 and temperature and pressure-are adapted to effect the removal of hydrogen sulfide and any light or low boiling hydrocarbons by means of line 16. A hydrofined lubricating oil product having a satisfactory color is withdrawn from zone 15 by means of line'17;
' The conditions in the hydrofining reactor are set forth in tabular form' below.
HYDROFINING CONDITIONS Preferred Range Temperature, F 500 450-550. Pressure. p.s.i.g 400 250-1500. Feed ate, v lhr lv 1.0 0.2-4.0. H feed, s.e.f./b 500 10-1000. H2 consumption, s.c.f./b less than 100. Water, lbs/b 2 .25-20.
phorus or zine compounds to the lubricating oil. These compounds are used in amounts of from 0.1% or less up to 4 Wt. percent. A process which would; improve color and protect the natural inhibitors would reduce or elimimate the need for these added inhibitors and therefore be a marked improvement in the art. a The object of this invention is to provide the-art with an improved hydrofining process for the improvement of color of lubricating oil. It is also the object of this invention to provide a method of improving the color of lubricating oil without the removal of sulfur. These and other objects will appear more clearly from the detailed specification and claims which follow.
It has now been found that petroleum lubricating oils can be upgraded, particularly with reference to color improvement, without removing an appreciable quantity of t In the present invention the introduction of either water introduction may be accomplished in several different manners. Either water or steam may be added separately as shown in the drawing o'rfeither may be added 'to the lubricating oil before the oil enters the reactor zone. If steam is used it may be added to the hydrogen before the hydrogen enters the reactor zone. When using water in the present invention, it is preferred to use distilled water, although ordinary undistilled water'ean be employed. If steam is used, it need only be at sufficient pressure to enter the system.
- The quantity of water used in the present invention may vary from .25 to 20 pounds of water per barrel of oil, although the preferred amount is about 2 pounds of water per barrel of lubricating oil feed. The exact explanation of why the addition of thewater improves the lubricating oil color is. not known. It appears that the water has the effect of making the catalyst more active. Accordingly, a very small quantity'ofwater is operable and the addition of large quantities of water do not seem to interfere with the improvement in color.
7 Stated another way. the quantity of water added may be based on the volume percent of water vapor in the hydrogen atmosphere during hydrofining. The quantity of water vapor in the hydrogen atmosphere is in the range of about 5 to 50 volume percent. The preferred amount is about 40 volume percent. When utilizing a continuous hydrofining system with a hydrogen gas rate of 100 to 1000 standard cubic feet per barrel of oil, 40 volume percent of water in the hydrogen atmosphere would correspond to a water content of approximately 2 to 20 pounds of water per barrel of lubricating oil feed. The amount of water shown in the examples which follow is approximately 40 volume percent or 2.2 pounds of water per barrel of lubricating oil feed.
The catalyst utilized in the present process may comprise known hydrofining catalysts. While the preferred catalyst of the present invention comprises cobalt molyb, date on alumina, or molybdenum sulfide on alumina, the use of a specific hydrofining catalyst is not required or considered essential to the invention. In the preferred cobalt molybdate catalyst, the amount of cobalt oxide is about 1% to 4% and of molybdenumoxide about 12% to 16% based on the weight of the catalyst. The molybdenum sulfide on alumina catalyst may consist of about to molybdenum sulfide based on the weight of the catalyst. The catalyst may be prepared by any known methods.
Regeneration of the catalyst may be required periodically depending largely. upon the nature of the feed stock. This regeneration is conveniently carried out at a temperature of about 900 F. with an oxygen containing gas.
The process of the present invention maybe more fully understood by the following examples illustrating the same.
Example I A dewaxed, non-extracted light lubricating oil distillate from Leduc type crude having the following inspections:
Inspection: Feed Gravity, APT 7 25.2 Viscosity 100 F., SUS 122 Tag Robinson Color 1% Aniline point, F.. 170 Sulfur, wt. percent 0.63
was hydrofined in a 2-liter laboratory autoclave using 163' grams of a catalyst consisting of 18 wt. percent molybdenum sulfide and 82 wt. percent gamma alumina. The pressure utilized was 400 p.s.i.g. and the temperature was 500 F. Each run was for a duration 'of five hours and 800 cc. of lubricating oil were charged in eachrun. The results of these runs are as follows:
drofining a lubricating. oil in. accord with the present invention, the color of the lube oil product is. materially improved by the addition of. water when hydrofining at a temperature of 500 F.
Example II In this example, the same type feed and hydrofining conditions as were used in Example I were employed. The catalyst used was 131 grams of a catalyst consisting of 14 wt. percent molybdenum oxide, 2.5 wt. percent cobalt oxide and 83.5 wt. percent gamma alumina. 800 cc.
of lubricating oil were again charged in each run. Care was taken to dry the catalyst and oil before Run No. 810.
cc. Water added to each charge Tag Pobinson Color Wt. percent 5 Run No. Sulfur The data of Example II clearly show that a marked improvement in lubricating oil color is obtained by the use of water in accord with this invention. Also, the data show that even though a color improvement is obtained at a temperature of 500 F. when using water, it. is ac-v complished with little or no removal of sulfur.
Example Ill The lubricating oil feed, catalyst, and hydrofining conditions employed in runs 713 and 714 are the same as those used in Example II, with the exception of the hydrofining temperature, which is noted below. Runs 813 to 816 are repeatedfrom Example II.
- Hydrofin- Tag Fob- Water, cc. ing Teminson penaiture Color Run No.
The information obtained from runs No. 713 and No. 714 shows that although improvement in color can be obtained. by hydrofining at a temperature of 600 F.,- the use of this relatively high temperature necessarily results in sulfur removal. The information obtained from runs No. 813 and No. 814 shows that hydrofining at 500 F. does not remove sulfur, but little color improvement is obtained. Runs No. 815 and No. 816 were made by hydrofining at a temperature of 500 F. using water in ace cord with the present invention and color improvement was obtained without sulfur removal.
The advantage of this invention will be apparent to those skilled in the art. Improved products of superior color characteristics can be obtained in a simple, economical process. The process provides a method of improving color without the removal of sulfur from the feed and thereby protects the natural oxidation inhibitors which are removed in normal hydrofining operation. This improvement is of such a simple nature, it can be added to existing hydrofining equipment with practically no cost.
It is understood that this invention is not limited to the specific examples which have been offered merely as illustrations and that modifications may be made with out departing from the spirit of the invention.
What is claimed is:
1. A process for upgrading and improving the color of a petroleum lubricating oil which'comprises hydrofining a lubricating oil feed boiling in the range of about 700 F. to 1100 F. at 760 mm. pressure at a temperature of about 450 to 550 F. and pressure of from about 250 to 1500 p.s.i.g'., in contact with a hydrofining catalyst and in the presence of a hydrogen atmosphere containing from about 5 to volume percent of water vapor thereby improving the color of the oil without removing an appreciable quantity of sulfur.
2. The process defined in claim 1 in which the hy-- drogen feed rate is in the range of 10 to 1000 standard cubic feet per barrel of lubricating oil feed.
3. A process for upgrading and improving the color of petroleum lubricating oil which comprises hydrofining a lubricating oil feed boiling in the range of about 700 F. to 1100 F. at 760 mm. pressure at a temperature of about 450 to 550 F. and pressure of from about 250 to 1500 p.s.i.g., in contact with a hydrofining catalyst and in the presence of added water in quantities ranging from about 0.25 to 20 pounds of water per barrel of lubricating oil feed thereby improving the color of the oil without removing an appreciable quantity of sulfur.
4. The process defined in claim 3 in which the hydrogen feed rate is in the range of 10 to 1000 standard cubic feet per barrel of oil lubricating feed.
6 5. The process defined in claim 4 where the water is added to the lubricating oil feed before hydrofining.
6. The process defined in claim 4 inwhich the water is added to the hydrofining process in the form of steam. 7. The proces defined in claim 6 in which the steam is added to the lubricating oil feed before hydrofining. 8. The process defined in claim 6 in which the steam is added to the hydrogen feed before hydrofining.
References Cited in the file of this patent UNITED STATES PATENTS 2,171,009 Rostin et al Aug. 29, 1939 2,428,532 Schulze et al Oct. 7, 1947 2,706,167 Harper et al Apr. 12, 1955 2,901,423 Herbert etal Aug. 25,- 1959
Claims (1)
1. A PROCESS FOR UPGRADING AND PIMPROVING THE COLOR OF A PETROLEUM LUBRICATING OIL WHICH COMPRISES HYDROFINING A LUBRICATING OIL FEED BOILING IN THE RANGE OF ABOUT 700*F. TO 1100*F. AT 760MM. PRESSURE AT A TEMPERATURE OF ABOUT 450* TO 550*F.AND PRESSURE OF FROM ABOUT 250 TO 1500 P.S.I.G., IN CONTACT WITH A HYDROFINING CATALYST AND IN THE PRESENCE OF A HYDROGEN ATMOSPHERE CONTAINING FROM ABOUT 5 TO 50 VOLUME PERCENT OF WATER VAPOR THEREBY IMPROVING THE COLOR OF THE OIL WITHOUT REMOVING AN APPRECIABLE QUANTITY OF SULFUR.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US741346A US3016350A (en) | 1958-06-11 | 1958-06-11 | Hydrofining lubricating oil |
| GB16212/59A GB846854A (en) | 1958-06-11 | 1959-05-12 | Improvements in hydrofining lubricating oil |
| FR797040A FR1237756A (en) | 1958-06-11 | 1959-06-09 | Improvements in hydrorefining lubricating oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US741346A US3016350A (en) | 1958-06-11 | 1958-06-11 | Hydrofining lubricating oil |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3016350A true US3016350A (en) | 1962-01-09 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US741346A Expired - Lifetime US3016350A (en) | 1958-06-11 | 1958-06-11 | Hydrofining lubricating oil |
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| Country | Link |
|---|---|
| US (1) | US3016350A (en) |
| FR (1) | FR1237756A (en) |
| GB (1) | GB846854A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3132089A (en) * | 1960-12-23 | 1964-05-05 | Union Oil Co | Hydrocracking process with pre-hydrogenation |
| US3227528A (en) * | 1962-03-12 | 1966-01-04 | Hydrocarbon Research Inc | High pressure reaction vessel |
| US3382168A (en) * | 1965-03-01 | 1968-05-07 | Standard Oil Co | Process for purifying lubricating oils by hydrogenation |
| US3501396A (en) * | 1969-04-14 | 1970-03-17 | Universal Oil Prod Co | Hydrodesulfurization of asphaltene-containing black oil |
| US4013637A (en) * | 1975-06-03 | 1977-03-22 | Exxon Research And Engineering Company | Water injection in a hydrodesulfurization process |
| US4021334A (en) * | 1974-08-08 | 1977-05-03 | Mobil Oil Corporation | Process for manufacture of stabilized lubricating oil with elemental sulfur |
| US20070295647A1 (en) * | 2006-06-22 | 2007-12-27 | Brownscombe Thomas F | Methods for producing a total product with selective hydrocarbon production |
| WO2007149922A1 (en) * | 2006-06-22 | 2007-12-27 | Shell Oil Company | Systems and methods for producing a total product with inorganic salt recovery |
| US20070295645A1 (en) * | 2006-06-22 | 2007-12-27 | Brownscombe Thomas F | Methods for producing a crude product from selected feed |
| US20100032342A1 (en) * | 2008-08-08 | 2010-02-11 | CleanOil Limited | Oil re-refining system and method |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2171099A (en) * | 1936-02-14 | 1939-08-29 | Hartmann-Riis Petter | Electrical control apparatus for heating plants |
| US2428532A (en) * | 1943-05-03 | 1947-10-07 | Phillips Petroleum Co | Catalytic hydrocarbon conversion process in the presence of steam |
| US2706167A (en) * | 1950-06-16 | 1955-04-12 | Sun Oil Co | Process for hydrogenating hydrocarbon oils |
| US2901423A (en) * | 1954-11-25 | 1959-08-25 | Metallgesellschaft Ag | Process for the hydrogenation of hydrocarbons |
-
1958
- 1958-06-11 US US741346A patent/US3016350A/en not_active Expired - Lifetime
-
1959
- 1959-05-12 GB GB16212/59A patent/GB846854A/en not_active Expired
- 1959-06-09 FR FR797040A patent/FR1237756A/en not_active Expired
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2171099A (en) * | 1936-02-14 | 1939-08-29 | Hartmann-Riis Petter | Electrical control apparatus for heating plants |
| US2428532A (en) * | 1943-05-03 | 1947-10-07 | Phillips Petroleum Co | Catalytic hydrocarbon conversion process in the presence of steam |
| US2706167A (en) * | 1950-06-16 | 1955-04-12 | Sun Oil Co | Process for hydrogenating hydrocarbon oils |
| US2901423A (en) * | 1954-11-25 | 1959-08-25 | Metallgesellschaft Ag | Process for the hydrogenation of hydrocarbons |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3132089A (en) * | 1960-12-23 | 1964-05-05 | Union Oil Co | Hydrocracking process with pre-hydrogenation |
| US3227528A (en) * | 1962-03-12 | 1966-01-04 | Hydrocarbon Research Inc | High pressure reaction vessel |
| US3382168A (en) * | 1965-03-01 | 1968-05-07 | Standard Oil Co | Process for purifying lubricating oils by hydrogenation |
| US3501396A (en) * | 1969-04-14 | 1970-03-17 | Universal Oil Prod Co | Hydrodesulfurization of asphaltene-containing black oil |
| US4021334A (en) * | 1974-08-08 | 1977-05-03 | Mobil Oil Corporation | Process for manufacture of stabilized lubricating oil with elemental sulfur |
| US4013637A (en) * | 1975-06-03 | 1977-03-22 | Exxon Research And Engineering Company | Water injection in a hydrodesulfurization process |
| US20070295647A1 (en) * | 2006-06-22 | 2007-12-27 | Brownscombe Thomas F | Methods for producing a total product with selective hydrocarbon production |
| WO2007149922A1 (en) * | 2006-06-22 | 2007-12-27 | Shell Oil Company | Systems and methods for producing a total product with inorganic salt recovery |
| US20070295645A1 (en) * | 2006-06-22 | 2007-12-27 | Brownscombe Thomas F | Methods for producing a crude product from selected feed |
| US20100032342A1 (en) * | 2008-08-08 | 2010-02-11 | CleanOil Limited | Oil re-refining system and method |
| US8088276B2 (en) * | 2008-08-08 | 2012-01-03 | CleanOil Limited | Oil re-refining system and method |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1237756A (en) | 1960-08-05 |
| GB846854A (en) | 1960-08-31 |
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