US2315935A - Stabilizing heavy fuel oil - Google Patents

Stabilizing heavy fuel oil Download PDF

Info

Publication number
US2315935A
US2315935A US352068A US35206840A US2315935A US 2315935 A US2315935 A US 2315935A US 352068 A US352068 A US 352068A US 35206840 A US35206840 A US 35206840A US 2315935 A US2315935 A US 2315935A
Authority
US
United States
Prior art keywords
sediment
fuel oil
oil
cracking
heavy fuel
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.)
Expired - Lifetime
Application number
US352068A
Inventor
William C Child
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Priority to US352068A priority Critical patent/US2315935A/en
Application granted granted Critical
Publication of US2315935A publication Critical patent/US2315935A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G31/00Refining of hydrocarbon oils, in the absence of hydrogen, by methods not otherwise provided for
    • C10G31/06Refining of hydrocarbon oils, in the absence of hydrogen, by methods not otherwise provided for by heating, cooling, or pressure treatment

Definitions

  • This invention relates to a method of improving heavy fuel oil, particularly cracking coil tar. It is concerned with stabilizing such fuels against sediment formation by a heat digesting treatment carried out under controlled conditions for a proper period, the temperature being held within determined limits related to the time of treatment.
  • pressure still tars or cracking coil tars The residua from pressure still or petroleum cracking units of various types, including those in which petroleum cracked stocks are heated in coils, are known as pressure still tars or cracking coil tars. They are ordinarily sufliciently fluid for flowing through pipes; they generally have suitably high flash points and high 13-. t. u. values, but they frequently contain appreciable percentages of coke-like and asphaltic materials, which are considered colloidally suspended, and which on standing tend to form undesirable sediments that make the oils containing them ill adapted for use as a fuel. This is particularly true when the cracking is intense and maximum yields of light products are desired.
  • the sediment formed in the fuel may be to various extents soluble or insoluble in light oils, such as benzene, naphtha, kerosene or gas oil, but it is very likely to precipitate out during storage or handling, owing to the behavior of carbonaceous bodies often referred to as free carbon, which have a tendency to flock out.
  • light oils such as benzene, naphtha, kerosene or gas oil
  • the object of the present invention is to provide a simple, economical, and efficient method for making a satisfactory reduction in the sediment forming tendency of heavy fuel oils.
  • a more specific object is to stabilize the heavy fuel oils, not only against precipitation of soluble sedi-- ment, but, also, against formation of insoluble sediment; and to accomplish this primarily without having to blend the fuel oil with large amounts of a more expensive light petroleum distillate, which also alters the high heating value characteristics of heavy fuel oil.
  • the light distillates moreover, cannot be employed without certain precautions in blending and selecting them because, in general, they usually tend to precipitate sludges from the pressure distillate tars at ordinary and moderately elevated temperatures, and unless they have a sufficiently high flash point entail the further expense of distilling the blend to obtain the proper flash point.
  • the sediment begins to increase just as cracking begins, hence, the maximum temperature is about 750 F., although it is preferred to restrict the maximum temperature to below 700 F., and particularly to 650 F.
  • the time should be at least hour and may go as high as 3 hours without detrimental cracking effects,
  • the initial material may be procured from the conventional types of cracking apparatus, as for example, directly from a separator drum receiving conversion products discharged from a cracking coil, from a flash zone that is connected to a separator drum, or intermediate withdrawal from the separator drum and flashing.
  • the tar may be subjected to the stabilization treatment in a tar pot connected with the cracking unit, or in a drum capable of withstanding pressure, like the autoclaves or closed bombs which were used experimentally.
  • the heat stabilization vessel may be heated internally or externally, or may be in the form of a heating coil which finally passes through a heat exchanger for cooling the stream of heavy oil conducted through the coil.
  • the initial tar may have an A. P. I. gravity below e. g. as low as 3 A. P. I., and as high as A. P. I.. and may have Saybolt i'urol viscosities from to 400 seconds at 122 F. to be made into marketable stabilized bunker fuel oil. Frequently, and more advisably for many uses, the tar should have a gravity of 8 A. P. I. to 14 A. P. I.
  • the stabilized fuel oil may be filtered or centrifuged, or may be doped with various colloidal fixing agents, if desired, but these additional steps, which are costly, are unnecessary for obtaining satisfactory products with the present process.
  • the fuel oil may be blended with any lighter or heavier oil to obtain any specified viscosity or gravity, for, as pointed out, the material treated in accordance with the present invention is not altered substantially with respect to viscosity and gravity.
  • the blending oil may be added as a quenching medium at the end of the stabilization heat treatment, and is preferably an oil of sufficiently high flash point to avoid forming a low flash .point blend.
  • the present treatment is of particular interest for recovering larger yields of higher quality fuel oils from the tarry products made by these processes.
  • the pressure still tar is given a reduction in total sediment even without being blended with a light distillate oil which further lowers the sediment at least partly by dilution or solution.
  • a method for producing a stabilized heavy fuel oil from a pressure still tar of petroleum of substantially the same gravity having a tendency to precipitate excessive quantities of sediment which comprises heating the initial pressure still tar without addition of lighter petroleum distillate oil to a temperature between about 450 F. and 750 F. for a period insufficient to cause cracking, ranging from 4 hour to 3 hours, while maintaining said tar under pressure.
  • the process of producing a stabilized heavy fuel oil which comprises heating a sedimentforming cracking coil tar of petroleum having an A. P. I. gravity in the range of 8 to 14, at a temperature in the range of 450 F. to 650 F. for a period of FA; hour to about 2 hours, under the autogenous pressure developed by vapors of said tar undiluted by a lighter petroleum distillate oil.
  • a method for stabilizing a sediment forming heavy fuel oil which comprises heating a sediment forming cracked residuum of petroleum, containing less than 10% hydrocarbons boiling below 500 F., at a temperature in the range of 450 F. to 750 F., under a pressure of vapors generated by heating said residuum unblended with a lighter distillate oil for a period sufiicient to substantially reduce the sediment forming content of the residuum, but insuflicient to change thePgravity of the residuum by more than 0.2 A.

Landscapes

  • 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

Patented Apr. 6, 1943 UNITED STABILIZING HEAVY FUEL OIL William 0. Child, Westfield, N. J., assignor to Standard Oil Development Company, a corporation of Delaware No Drawing. Application August 10, 1940, Serial No. 352,068
Claims. (01. 196-75) This invention relates to a method of improving heavy fuel oil, particularly cracking coil tar. It is concerned with stabilizing such fuels against sediment formation by a heat digesting treatment carried out under controlled conditions for a proper period, the temperature being held within determined limits related to the time of treatment.
The residua from pressure still or petroleum cracking units of various types, including those in which petroleum cracked stocks are heated in coils, are known as pressure still tars or cracking coil tars. They are ordinarily sufliciently fluid for flowing through pipes; they generally have suitably high flash points and high 13-. t. u. values, but they frequently contain appreciable percentages of coke-like and asphaltic materials, which are considered colloidally suspended, and which on standing tend to form undesirable sediments that make the oils containing them ill adapted for use as a fuel. This is particularly true when the cracking is intense and maximum yields of light products are desired. The sediment formed in the fuel may be to various extents soluble or insoluble in light oils, such as benzene, naphtha, kerosene or gas oil, but it is very likely to precipitate out during storage or handling, owing to the behavior of carbonaceous bodies often referred to as free carbon, which have a tendency to flock out.
The sediment in a heavy fuel oil gives rise to great difficulties in plugging fuel lines, burners, sticking of valves, etc. thus, making the fuel diflicult to employ and unmarketable. Hence, a number of attempts have been made to counteract the formation of sediment in the heavy fuel oils, for example, removal of the sediment by filtration or centrifuging, by addition of a substance, e. g., rosin, purported to stabilize the colloidal sediment, or by the addition of lighter oils to solubilize part of the sediment but by which the heating value and flash point of the fuel are lowered. It is apparent, however, that such proposed methods alter the character of the fuel oil and are not economically feasible.
The object of the present invention is to provide a simple, economical, and efficient method for making a satisfactory reduction in the sediment forming tendency of heavy fuel oils. A more specific object is to stabilize the heavy fuel oils, not only against precipitation of soluble sedi-- ment, but, also, against formation of insoluble sediment; and to accomplish this primarily without having to blend the fuel oil with large amounts of a more expensive light petroleum distillate, which also alters the high heating value characteristics of heavy fuel oil. The light distillates, moreover, cannot be employed without certain precautions in blending and selecting them because, in general, they usually tend to precipitate sludges from the pressure distillate tars at ordinary and moderately elevated temperatures, and unless they have a sufficiently high flash point entail the further expense of distilling the blend to obtain the proper flash point.
The foregoing objects and advantages have been attained in accordance with the present invention, which is based on my discovery, that when a heavy fuel oil, such as derived from a cracking operation on reduced crudes or gas oils under severe cracking conditions, is heated in a closed container, e. g. a closed bomb, autoclave, or pressure vessel, over certain periods of time at definite temperatures within the range of 450 F. to 750 F., then cooled to below 450 F. an excellent decrease in sediment formation, both of soluble and insoluble kinds, was obtained. In the bomb the fuel oil was heated in the absence of air without substantial distillation.
In no case was more than a trace of coke formed in the bomb at the end of a run, therefore the sediment reduction could not be attributed to settling therein. At temperatures below 650 F. no coke at all was found. The optimum conditions are somewhat difilcult to define, because in all runs made for periods of A; hour to 2 hours at temperatures below 650 F. the sediment reduction was of the same order of magnitude, but the more striking results were obtained in the range of 550 F. to 650 F. with the heating period varying inversely with the temperature and being about 2 hours to hour.
Another indication of the maximum severity of conditions in the heating treatment stabilization, beside that of coking in the bomb and the analytical results of sediment reduction, is that of the constancy in gravity and viscosity of the treated material. proper temperatures of treatment, the sediment reduction was effected with no substantial change in gravity, the variation being at the most only about 0.l A. P. I. to 02 A. P. I., mainly not more than (3.1 A. P. 1.; and the viscosity in Saybolt furol seconds at 122 F. only varied about 0.1 second to about 5 seconds. In effect, these small changes confirm that no substantial cracking nor viscosity breaking occurs in the stabilization treatment.
By the present method of heavy fuel oil sta- It was found that at the bilization, cracking coil tar, or even bottoms of reduced crude tars, having low A. P. I. gravities and containing too much sediment and sludge after a short period of standing to be used as liquid fuels, are greatly improved in lowering of their insoluble solid impurities as shown by the A. S. T. M, tests using the centrifuging (B. S. and W.) andfiltration (Insol.-Sed.') methods, wherein the fuel is treated with a light oil that At above 650 F., and more particularly at from 700 F. to 750 F., the sediment begins to increase just as cracking begins, hence, the maximum temperature is about 750 F., although it is preferred to restrict the maximum temperature to below 700 F., and particularly to 650 F. At the minimum temperatures of about 450 F. the time should be at least hour and may go as high as 3 hours without detrimental cracking effects,
extracts much of the sediment. Furthermore, 1 but, as stated before, the optimum conditions using a more advanced test which detects by :are 500 F. to 650 F. for a period of A hour to filtration, sediment in the viscous oil per se, 2 hours.
i. e. undiluted with light oils, which under prac- It has been observed that heat treatments of tical conditions would not be present since they pressure still tars under incipient cracking conimpair the flash point of the fuel, the :total reditions, as for example, by laboratory methods duction of insoluble sediment which is actually used in determining the effect of cracking conmade can be shown to be obtained by thepresent ditionson sediment formation, are not useful process to a high degree. In this test, known as for stabilizing cracking still tars, because by these the hot filtration sediment test, the straight methods, the still is held at 650 F. to 800 F. for heavy fuel oil, undiluted, is filtered at about a-period of 4 hours to 6 hours, and this treatment 212 F. through a weighed Gooch filter bearing tends to concentrate the bottoms and produce an asbestos mat, and the total amount .of sedimoresediment forming bodies. Similarly, apresment is weighed and determined in percentage sure still .tar passed directly to tar receptacles, of the -oil.f1ltered. To demonstrate the resulting where they undergo substantial flashing or reimprovement from various pressure .still tars ductionby vaporizationand in which .time and stabilized by the treatment illustrated in this temperature are not properly controlled, give invention, the test.data.is.shown in thefollowing rise to anincreasein sedimentforming bodies. table: Hence, it is to be understood that in theheat Temperature .Y-F.. 450 550 Time of run hrs 2 2 Stock Feed Prod. Feed .Prod. Feed Prod Feed Prod.
Gray -344. .L. 13.1 13.1 12.9 13.0 13.1 13.2 13.10 13.0
ssr "115.5312 1 42.4 42.5 42.0 42.3 41.8 41.7 42.0 42.7
13. send wperccnt. 1.2 0. 0 1. 4 0.0 1.2 0.4 1. 2 0.4
Temperature F 600 650 Time of run l1rs 2 M 2 Prod Feed Prod. Feed Prod. Feed Prod.
13. 0 13. 0 12. 3 12. 9 12.8 13. 0 13.1 .43. 0 42. 0 42.5 45. 2 41. 5 43. 0 3s. 1 0.3 1.2 0.3 1.0 0.4 1.4 0.0 0.087 0.139 0. 005 0. 214 0. 111 0. 172 0. 0. 117 1.0-124 .i 0. 103 0. 030 0.081 0. 245 0. 130, 0. 270 0. o. 290 0. 230
Temperature K... 700-740 750 Timeo'irun hrs-; 1 V2 2 Stock Feed Prod Feed Prod. .Feed Prod Feed Prod.
Grav .941. r. 1-. 13-4 13. 0 13. 0 12. 9 13. 0 12.7 13. 0 12. 0
SS]? "visa: 122 50. 7 57.0 43. 0 .30. 0 43. 0 41. 0 43.0 43. 4
B. s. and W- pereer1t 0. 3 1. 4 1.3 0. 0 1. 3 1. 5 1.3 2. 0
111501. sed do 0.109 1 0.109 0. 131 0. 148 0.202 1 0.250 0. 100 1 0. 854
Red.-in insolrsed .;do 0.060 0.033 0.054 ,-0.,694
Sad. by hot 0m "00.--. 0. 120 1 0. 395 0. 20 1 0. 27 0. 23 1 o. 57 0. 20 1 1. 05
1 Increases in sediment denoted.
The data clearly shows the'benefioial effect of stabilization treatment it is desirable .to mainthe heat stabilization treatment and illustrates tain the heavy fuel oil under sufiicient pressure that no substantial cracking accompanied the to-avoid substantial vapor-ization,and more parreduction in sediment, in that no substantial ticularly under the autogenous pressure created change in viscosity or gravity was made, while 7 by vapors of the oil or tar in a closed vesselwiththe total sediment-content was substantially .and out vapor withdrawal. .Any partial pressure permanently-reduced. In theruns madeat above added by the presence of .an inert or reducing 700 as the time .of treatment exceeded /4 gasis permissible, but, ofcourse, it is desirable hour, the sediment forming tendency was .into avoid the presence of oxidizing gases. creased as denoted. 75 The initial pressure still tar, or heavy fuel oil,
to be stabilized can be treated just after recovery in a cracking unit, or at some time thereafter. The initial material may be procured from the conventional types of cracking apparatus, as for example, directly from a separator drum receiving conversion products discharged from a cracking coil, from a flash zone that is connected to a separator drum, or intermediate withdrawal from the separator drum and flashing. The tar may be subjected to the stabilization treatment in a tar pot connected with the cracking unit, or in a drum capable of withstanding pressure, like the autoclaves or closed bombs which were used experimentally.' The heat stabilization vessel may be heated internally or externally, or may be in the form of a heating coil which finally passes through a heat exchanger for cooling the stream of heavy oil conducted through the coil. The initial tar may have an A. P. I. gravity below e. g. as low as 3 A. P. I., and as high as A. P. I.. and may have Saybolt i'urol viscosities from to 400 seconds at 122 F. to be made into marketable stabilized bunker fuel oil. Frequently, and more advisably for many uses, the tar should have a gravity of 8 A. P. I. to 14 A. P. I.
After the heat stabilization treatment, the stabilized fuel oil may be filtered or centrifuged, or may be doped with various colloidal fixing agents, if desired, but these additional steps, which are costly, are unnecessary for obtaining satisfactory products with the present process. Also, the fuel oil may be blended with any lighter or heavier oil to obtain any specified viscosity or gravity, for, as pointed out, the material treated in accordance with the present invention is not altered substantially with respect to viscosity and gravity. The blending oil may be added as a quenching medium at the end of the stabilization heat treatment, and is preferably an oil of sufficiently high flash point to avoid forming a low flash .point blend.
Since a yield advantage exists in running oils to a low A. P. I. gravity tar with increased intensity of cracking, but which alsoincreases insoluble sediment in the tar, the present treatment is of particular interest for recovering larger yields of higher quality fuel oils from the tarry products made by these processes. By the treatment of the present process, the pressure still tar is given a reduction in total sediment even without being blended with a light distillate oil which further lowers the sediment at least partly by dilution or solution.
The exact mechanism of the stabilization treatment is not understood, but in accordance with the colloidal theory, it appears that the controlled digestion of the tarry oil causes protective asphaltic compounds therein to envelop and disperse the sediment-forming carbonaceous bodies and, therefore, prevents their flocculation.
My invention is not to be limited by any theory or mechanism, nor to any specific example given for the purposes of illustration.
Iclaim:
1. A method for producing a stabilized heavy fuel oil from a pressure still tar of petroleum of substantially the same gravity having a tendency to precipitate excessive quantities of sediment, which comprises heating the initial pressure still tar without addition of lighter petroleum distillate oil to a temperature between about 450 F. and 750 F. for a period insufficient to cause cracking, ranging from 4 hour to 3 hours, while maintaining said tar under pressure.
2. The process of producing a stabilized heavy fuel oil which comprises heating a sedimentforming cracking coil tar of petroleum having an A. P. I. gravity in the range of 8 to 14, at a temperature in the range of 450 F. to 650 F. for a period of FA; hour to about 2 hours, under the autogenous pressure developed by vapors of said tar undiluted by a lighter petroleum distillate oil.
3. The process of producing a stabilized heavy fuel oil which comprises heating a reduced cracking coil tar of petroleum containing less than 10% of hydrocarbons boiling below 500 F. at a temperature in the range of 450 F. to 650 F. for a period of A; hour to about 2 hours without substantial separation of vapors and without addition of a lighter distillate oil, then immediately thereafter cooling said heated tar to below 450 F.
1 4. A method for stabilizing a sediment forming heavy fuel oil which comprises heating a sediment forming cracked residuum of petroleum, containing less than 10% hydrocarbons boiling below 500 F., at a temperature in the range of 450 F. to 750 F., under a pressure of vapors generated by heating said residuum unblended with a lighter distillate oil for a period sufiicient to substantially reduce the sediment forming content of the residuum, but insuflicient to change thePgravity of the residuum by more than 0.2 A. I.
5. A method as described in claim 3, in which the stabilized heavy fuel oil formed by the heat treatment is blended with a lighter oil to form a blend of higher A. P. I. gravity.
WILLIAM C. CHILD.
US352068A 1940-08-10 1940-08-10 Stabilizing heavy fuel oil Expired - Lifetime US2315935A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US352068A US2315935A (en) 1940-08-10 1940-08-10 Stabilizing heavy fuel oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US352068A US2315935A (en) 1940-08-10 1940-08-10 Stabilizing heavy fuel oil

Publications (1)

Publication Number Publication Date
US2315935A true US2315935A (en) 1943-04-06

Family

ID=23383663

Family Applications (1)

Application Number Title Priority Date Filing Date
US352068A Expired - Lifetime US2315935A (en) 1940-08-10 1940-08-10 Stabilizing heavy fuel oil

Country Status (1)

Country Link
US (1) US2315935A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2417236A (en) * 1945-01-02 1947-03-11 Standard Oil Dev Co Heating oil
US2951037A (en) * 1953-12-30 1960-08-30 British Petroleum Co Reduction of sludge deposition from crude oils
US3006842A (en) * 1958-07-23 1961-10-31 British Petroleum Co Method for reducing sludge deposition of fuel oils
US3027319A (en) * 1954-06-29 1962-03-27 British Petroleum Co Reduction of sludge deposition from crude oils
US3284336A (en) * 1965-06-10 1966-11-08 Oil Shale Corp Method of treating oils derived by thermal treatment of solid carbonaceous materials
US4446002A (en) * 1982-08-05 1984-05-01 Exxon Research And Engineering Co. Process for suppressing precipitation of sediment in unconverted residuum from virgin residuum conversion process
US4488957A (en) * 1981-06-01 1984-12-18 Koa Oil Company, Ltd. Method and apparatus for production of crystallizable carbonaceous material
US4882041A (en) * 1986-03-06 1989-11-21 Delta Projects Inc. Diluent substitution process

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2417236A (en) * 1945-01-02 1947-03-11 Standard Oil Dev Co Heating oil
US2951037A (en) * 1953-12-30 1960-08-30 British Petroleum Co Reduction of sludge deposition from crude oils
US3027319A (en) * 1954-06-29 1962-03-27 British Petroleum Co Reduction of sludge deposition from crude oils
US3006842A (en) * 1958-07-23 1961-10-31 British Petroleum Co Method for reducing sludge deposition of fuel oils
US3284336A (en) * 1965-06-10 1966-11-08 Oil Shale Corp Method of treating oils derived by thermal treatment of solid carbonaceous materials
US4488957A (en) * 1981-06-01 1984-12-18 Koa Oil Company, Ltd. Method and apparatus for production of crystallizable carbonaceous material
US4446002A (en) * 1982-08-05 1984-05-01 Exxon Research And Engineering Co. Process for suppressing precipitation of sediment in unconverted residuum from virgin residuum conversion process
US4882041A (en) * 1986-03-06 1989-11-21 Delta Projects Inc. Diluent substitution process

Similar Documents

Publication Publication Date Title
US4615791A (en) Visbreaking process
US2315935A (en) Stabilizing heavy fuel oil
RU2333932C1 (en) Method of electrochemical cracking of heavy oil products
US2009710A (en) Method of removing ash-forming components from crude petroleum oil
US3284336A (en) Method of treating oils derived by thermal treatment of solid carbonaceous materials
US2762754A (en) Thermal conversion of reduced crudes
EP0090897A2 (en) Delayed coking of a heat-treated ethylene tar
US2199841A (en) Method of treating hydrocarbon mixtures
US2273147A (en) Decolorization of mineral oils
US1966801A (en) Coking hydrocarbon oils
US2048371A (en) Blending of mineral oils and residues
US2246760A (en) Stable fuel oil
US2049000A (en) Manufacture of asphalt and lubricating oils
US1708602A (en) Process for making a fluorescent product
US2049014A (en) Process of improving lubricating oil
US2716085A (en) Adhesive petroleum lubricant
US2200534A (en) Low pour point lubricating oil
US1708563A (en) Process of imparting fluorescence to oil
Savaya et al. Stability of fuel oils produced by visbreaking of vacuum residue
US1721719A (en) Of los
US2315077A (en) Method of treating slack wax
US1859514A (en) Certificate of correction
US2114467A (en) Improved process for separating wax from hydrocarbon oils containing the same
US2218649A (en) Treatment of cracked residuum
US2058696A (en) Process of stabilizing oils