US3293173A

US3293173A - Color improvement of petroleum lubricating oils

Info

Publication number: US3293173A
Application number: US386710A
Authority: US
Inventors: Patrick P Mccall
Original assignee: Exxon Research and Engineering Co
Current assignee: ExxonMobil Technology and Engineering Co
Priority date: 1964-07-31
Filing date: 1964-07-31
Publication date: 1966-12-20
Anticipated expiration: 1983-12-20
Also published as: BE667789A; GB1094940A; NL6509507A; DE1545275A1; NO119955B

Description

P. P. MCcALL 3,293,173

COLOR IMPROVEMENT OF PETROLEUM LUBRICATING OILS Dec. 20, 1966 Filed July 31, 1964 INVENTOR Patrick P. McColl PATENT ATTORNEY stocks.

United States Patent 3,293,173 COLGR IMPRVEMENT F PETRLEUM LUBRICATING OILS Pah-ick P. McCall, Madison rIownship, Middlesex County,

NJ., assigner to Esso Research and Engineering Company, a corporation of Delaware Fiied .luiy 31, 1964, Ser. No. 386,7i0 7 Claims. (Cl. 20S- 264) This invent-ion relates to upgrading and improving the color and stability of petroleum lubricating oil base More particularly, the invention relates to a process wherein unfinished or untreated lubricating oil stocks are first hydroined and then distilled over alkali metal or alkaline earth metal hydroxides.

The treatment of lpetroleum lubricating oil base stocks with aqueous caustic or lime is well yknown in the art. The hydroning of lubricating oils is well known in the art. It is also known to treat certain lubricating oils with excess caustic or lime and then to hydrofne the lubricating oils. Certain raw or untreated lubricating oil stocks can be given a single treatment of either hydrofining or caustic or lime treatment to achieve sufficient improvement in color, color stability, etc., `t-o meet the specifications set down for finished lubricating oil base stocks in certain of the less demanding applications. However, there are other lubricating oil base stocks which need more than one single processing step.

It has been known that petroleum lubricating oil-s can be upgraded by treating them first with excess alkali metal or alkaline earth metal hydroxide, distilling the oil from the treatin-g medium 'and then hydrofining the distilled oil in the presence of hydrogen and a hydrofining catalyst.

It has now been found that petroleum lubricating oils can be upgraded by first hydrofinfing the oil. in the presence of hydrogen and a hydrofining catalyst, and then treating the hydrofined oil with solid alkali metal or alkaline earth metal hydroxide at an elevated temperature and distilling the hydrofined oil over excess alkali metal or alkaline earth metal hydroxide gives an unexpected additional benefit and results in improved oil color and in the greatest degree of color stability irnprovement.

The .figure is a `grap-h representing the results of various treatments `and compares the color stabilities of the products obtained from these treatments.

The petroleum lubricating stocks to be treated are distillates fallin-g within the boiling range of about 650 F. to 900 F., a viscosity in the range of Iabout 36 to 130 S.S.U. at 210 F. The lubricating base stock is preferably one derived from napht'henic base crude oils such as Tia Juana, Coastal, Lagun-illas, etc. However, the invention is not restricted to this class of crude petroleum oils since advantages are also obtained by treating base stocks derived -frorn paraffin base crude oils. The lubricating oils which may be treated according to this invention include transformer oils, spindle oils, machine oils, base stocks -for grease manufacture, and cutting oils.

The lubricating oil stock can be hydrofined under the following condition-s:

The hydrofining catalysts that can be used in the hydrofining step include conventional hydrofining catalyst such as cobalt molybdate on alumina, molybdenum oxide on alumina, nickel sulfide, tungsten sulfied, nickel-cobaltmolybdenum on alumina, iron-cobalt-miolybdenum on alumina. The cobalt molybdate catalyst comprises 2-6 wt. percent of cobalt oxide and y6-15 wt. percent of molybdenum oxide. The catalyst is preferably used in a fixed bed. Regeneration of the catalyst bed to remove carbonaceous deposits is periodically carried out with an 0 oxygen-containing gas such as air or one in which the oxygen content may be lower or higher than in air. The regeneration is carried out at a temperature between about 750 F. and 1000 F.

In the hydrofining operation, the lubricating oil and 5 hydrogen are contacted with a fixed bed of catalyst in a reactor vessel by continuous downward flow through the vessel. The -oil feed to the reactor vessel is preheated by means of a furnace, heat exchangers or other means to a temperature between about 500 F. to 700 F. The hydrogen may or :may not be preheated. After the hydrofning step has been carried out, the treated lubricating oil `stock is passed to a steam stripping column to remove residual hydrogen and H28.

The stripped lubricating oil is then reheated, vaiporized and `distilled under reduced pressure in a vacuum rerun tower under conditions which result in at least and preferably or more of the oil being taken overhead or as sidestream cuts. During the course of this distillation, a controlled amount of alkali metal or alkaline earth metal hydroxide is introduced and mixed with the oil in such a way as to provide intimate contact between the oil and a dispersion of finely divided particles of solid caustic material. The caustic material ultimately leaves the system as a finely divided solid suspension in the bottom-s Ifrom the vacuum rerun tower.

The desired contact between the oil and the solid caustic material can conveniently be accomplished as follows. The stripped lubricating oil stock is mixed with an aqueous metal hydroxide. An aqueous solution of sodium hydroxide or an aqueous slurry of lime or calcium oxide is preferred as these are the c-heapest. Potassium hydroxide may be used. W'hen using aqueous sodium hydroxide, the concentration of the solution is between about 10 B. and 50 B. which is equivalent to about 7 wt. percent to 50 wt. percent of Sodium hydroxide in Water. A 50 B. aqueous sodium hydroxide is preferred. The amount of sodium hydroxide used is between about .0005 and .0l part by weight per part by weight of lubricating oil, preferably about .006 part by weight per part by weight of the lubricating oil of the preferred concentration of aqueous solution of sodium hydroxide. When using a water slurry of lime or calcium oxide, about twice as much of the lime or calcium hydroxide as sodium hydroxide is used.

The stripped lubricating oil is heated in a preheat furnace and the aqueous solution of sodium hydroxide or aqueous suspension of lime or calcium hydroxide may be introduced -into the :stripped lubricating oil stream before or after but preferably before the heating step in the preheat furnace. Steam is also added to the stripped lubricating oil stream, preferably ahead of the pre-heat furnace. The oil is at a temperature of about F. to 600 F., preferably 500 F., and, after heating, it has a temperature of between about 725 F. and 775 F., preferably 750 F. The time of contact of the oil and metal hydroxide solution above about 700 F. in the preheat furnace is between about 30 and 300 seconds.

The thus treated oil is then separated from the spent metal hydroxide solution by `distillation under reduced pressure in a vacuum rerun tower. The pressure in the rerun tower is between about 75 and 150 mm. Hg abso- A raw Tia Juana lubricating oil distillate of high neutralization number of 0.95 mg. KOH/ g. and high sulfur content (1.8 wt. percent) and having the characteristics given in Table II was hydroiined at 575 F., 800 p.s.i.g. pressure, hydrogen-containing gas (60% by volume H2) used was 500 s.c.f./b. of feed, and the space velocity was 1.0 v./hr./v. (volume of oil per hour per volume of catalyst). The hydroned oil was steam stripped to remove H2 and H28. A portion of this hydroned oil was distilled over 0.25 wt. percent solid NaOH -in .a batch vacuum distillation apparatus at a pressure of about l mm. Hg absolute. About 97 volume present of the lubricating oil feed was recovered.

In Table II, results are given for caustic distillation only of the Tia luana lubricating oil feed with recovery of 95% by volume of the feed. The treatment was by distillation over solid caustic. The concentration of the caustic and the amount used per part of oil are the same as in the caustic treatment above described in connection with the hydrolining-caustic treating combination of the present invention.

In Table II, results are also given for the reverse combination, that is, the lubricating oil is first caustic treated and then hydroned with a recovery of 95% by volume of treated oil. The caustic treat and hydroiining were the same as given in the hydroiining-caustic treatment of the present invention. i

TABLE II Raw /957 O/957 0/977 Tr 102 Hydra onL7 ono ont(7 Distilfined 1 Cautic Caustic Hydro 1 late Only Distilled -I- Hydrol Caus- Only tic Gravity, API 19. 5 20. 4 19. 7 20 20. 5 Vis/100; F., SSTL..-" l, 944 1, 622 l, 685 1, 635 l, 469 Vis/210 F., 95. l 88. 6 89. 7 88. 2 84. 6 Viscoslty Index. 34 39 37 37 39 Color, ASTM 6. 3. 4 5. 4 3. 3 3. 2 Colorhold, ASTM 2 8 4. 4 5. 9 4. 3 3. 7 Pour Point, F +5 0 -5 -15 -15 1All Hydroning done 575 F., S00 psig., 500 s.c.f./b. ol 60% H2 treat gas, 1 v./v./hr.

2 Color after accelerated aging of oil at 212 F. for 16 hours.

From the above results it will be seen that the combination of steps of iirst hydroiining the lubricating oil distillate stock and then treating or distilling it over solid caustic material produces the maximum improvement in color and color stability. With the present invention, a more stable lubricating oil product is obtained than when the reverse steps are used and hydrotining is the last step. If the caustic treatment comes before the hydroning step, the improvement in stability is nullied. The effects of the two stages are beneficial only when done in the proper order.

It is essential that the caustic treatment or metal hydroxide treatment of the hydroiined lubricating oil stock be with solid metal hydroxide and at a temperature above about 400 F.

Example II Lube oil distillates from Tia I nana 102` crude were subjected to a variety of treatments involving hydroiinring alone, rerunning over caustic alone, rerurming over caustic followed by hydroiining, and hydroiining followed by re- 4 running over caustic. Some but not all of the data is included in Table II. In the iigure, the color stabilities of the products obtained from these treatments are compared. On this graph are plotted the initial colors of the oils immediately after treatment vs. the color obtained on each sample after accelerated aging for 16 hours at 212 F. The data are plotted on logarithmic paper using a scale which is proportional to color-body concentration.

It can be seen that the data fall into two groups: (1) those stocks for which the .iinal treatment was hydroiining either as one step or as the second step; and (2) those stocks for which the nal treatment was rerunning over caustic either as one step or as the second step. In all cases, the caustic-rerun-last stocks showed better color stability than the hydroiined-last stocks. On the average, the caustic-rerun-last stocks increased in color concentration by a factor of 1.25 during the accelerated aging test, significantly less than the hydroned-last stocks, which averaged a 1.65-fold increase. The data from Example l are shown on this graph also, to illustrate their consistency. It is thus apparent that rerunning over caustic leads to better color stability than does hydroiining, and that when the two steps are combined in the proper sequence, namely, hydroi'ining followed by rerunning over caustic, the greatest improvement in color (achieved primarily by the hydroning step) and color stability (achieved primarily by the caustic rerunning step) results.

It is to be understood that the invention is not limited to the specic examples which are included merely as illustrations of the invention and that modifications may be made without departing from the spirit of the invention.

What is claimed is:

1. A process for improving the color and color stability of a petroleum lubricating oil base stock which comprises hydroning the lubricating oil base stock in the presence of a hydroiining catalyst and hydrogen, introducing an aqueous alkaline metal hydroxide into the hydrolined oil, said metal hydroxide being selected from the group consisting of hydroxides of the alkali metals and alkaline earth metals and being used in an amount between .0005 and .01 part by weight per part of oil by weight, heating the resulting mixture of oil and metal hydroxide to a temperature between about 400 F. and 700 F. to vaporize and separate the water from the non-volatile solid metal hydroxide, distilling the oil under vacuum in a vacuum rerun tower in direct contact with the separated solid metal hydroxide to produce a lubricating oil stock of improved color and color stability.

2. A process for improving the color and color stability of petroleum lubricating oil base stock which comprises catalytically hydroiining the oil base stock at a temperature in the range between 500 F. and 700 F. and at a pressure in the range between and 1500 p.s.i.g., steam stripping the hydroined oil, then treating the hydroiined oil with an aqueous metal hydroxide at a temperature between about 400" F. and 700 F., said hydroxide being selected from the group consisting of hydroxides of alkali metals and alkaline earth metals, the amount of aqueous metal hydroxide used being between about .0005 and .01 part by weight per part by weight of oil and the concentration of the aqueous metal hydroxide being between about 7 and 50 B and the time of contact of said hydrotined oil and said metal hydroxide is between about 30 and 300 seconds, distilling the treated oil from the metal hydroxide under reduced pressure in a vacuum rerun tower, during said distillation directly contacting said hydrolined oil with solid metal hydroxide left behind in said vacuum rerun tower to produce a lubricating oil stock of improved color and color stability and recovering said lubricating oil stock of improved color and color stability as a sidestream from said vacuum rerun tower as product.

3. A process according to claim 2 wherein saidvhydroxide comprises sodium hydroxide.

4. A process according to claim 2 wherein said distillation step is carried out under a reduced pressure between 5 about 1 and 150 mm. Hg absolute in said vacuum rerun tower.

5. A process according to claim 2 wherein spent alkaline metal hydroxide is withdrawn in the bottoms oil fraction from the bottom of said vacuum rerun tower.

6. A process for improving color and color stability of a petroleum lubricating oil base stock which comprises hydrofining the lubricating oil base stock in the presence of a hydroning catalyst and hydrogen, then contacting said hydroned oil with an alkaline metal hydroxide, said metal hydroxide being selected from the group consisting of hydroxides of the alkali metals and alkaline earth metals, heating said hydroned oil in said contacting step to a temperature between about 400 F. and 700 F., then distilling said hydroned oil under vacuumV in a vacuum rerun tower in direct contact with said alkaline metal hydroxide to produce a lubricating oil stock of improved color and color stability.

6 7. A process according to claim 6 wherein the time of contacting said hydroned oil and alkaline metal hydroxide tis between about 30 and 300 seconds at a temperature of about 700 F. and the amount of alkaline metal hydroxide is between about .0005 and .01 part by Weight per part by weight of oil feed.

References Cited by the Examiner UNITED STATES PATENTS 1,932,369 10/1933 Guthke 208-215 2,944,014 7/ 1960 Holman 208-264 3,121,678 2/ 1964 Behymer et al 208-212 3,128,155 4/1964 Mattox 208-212 DELBERT E. GANTZ, Primary Examiner. S. P. JONES, Assistant Examiner.

Claims

1. A PROCESS FOR IMPROVING THE COLOR AND COLOR STABILITY OF A PETROLEUM LUBRICATING OIL BASE STOCK WHICH COMPRISES HYDROFINING THE LUBRICATING OIL BASE STOCK IN THE PRESENCE OF A HYDROFINING CATALYST AND HYDROGEN, INTRODUCING AN AQUEOUS ALKALINE METAL HYDROXIDE INTO THE HYDROFINED OIL, SAID METAL HYDROXIDE BEING SELECTED FROM THE GROUP CONSISTING OF HYDROXIDES OF THE ALKALI METALS AND ALKALINE EARTH METALS AND BEING USED IN AN AMOUNT BETWEEN .0005 AND .01 PART BY WEIGHT PER PART OF OIL BY WEIGHT, HEATING