US2332793A - Refining of mineral oils - Google Patents
Refining of mineral oils Download PDFInfo
- Publication number
- US2332793A US2332793A US367907A US36790740A US2332793A US 2332793 A US2332793 A US 2332793A US 367907 A US367907 A US 367907A US 36790740 A US36790740 A US 36790740A US 2332793 A US2332793 A US 2332793A
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- Prior art keywords
- acid
- oil
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- water
- solution
- 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
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- 239000002480 mineral oil Substances 0.000 title description 6
- 238000007670 refining Methods 0.000 title description 5
- 239000002253 acid Substances 0.000 description 58
- 239000003921 oil Substances 0.000 description 49
- 239000000470 constituent Substances 0.000 description 26
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical class S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- 239000000243 solution Substances 0.000 description 19
- 238000009835 boiling Methods 0.000 description 12
- 239000010802 sludge Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 239000003208 petroleum Substances 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 8
- 239000000446 fuel Substances 0.000 description 7
- 150000003464 sulfur compounds Chemical class 0.000 description 6
- 230000002378 acidificating effect Effects 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 239000003513 alkali Substances 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- OGNVQLDIPUXYDH-ZPKKHLQPSA-N (2R,3R,4S)-3-(2-methylpropanoylamino)-4-(4-phenyltriazol-1-yl)-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid Chemical compound CC(C)C(=O)N[C@H]1[C@H]([C@H](O)[C@H](O)CO)OC(C(O)=O)=C[C@@H]1N1N=NC(C=2C=CC=CC=2)=C1 OGNVQLDIPUXYDH-ZPKKHLQPSA-N 0.000 description 1
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical compound OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 description 1
- 229940012189 methyl orange Drugs 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 238000000926 separation method Methods 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
- C10G17/00—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge
- C10G17/02—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge with acids or acid-containing liquids, e.g. acid sludge
- C10G17/04—Liquid-liquid treatment forming two immiscible phases
- C10G17/06—Liquid-liquid treatment forming two immiscible phases using acids derived from sulfur or acid sludge thereof
Definitions
- the present invention relates to the refining of mineral oils.
- the invention is more particularly concerned with the refining of petroleum oils boiling in the motor fuel, kerosene, and gas oil boiling ranges, and especially relates to an improved process for the removal of objectionable compounds therefrom, when utilizing as a treating agent a mineral acid such as a sulfuric or an equivalent acid.
- acid treated oils after the removal of the acid sludge, are subjected in an initial stage to a weak acid treatment, and then treated in the secondary stage with a washing solution which preferably comprises water.
- the treated oil isthen neutralized with a suitable alkali, as for example an aqueous caustic solution in order to produce an improved refined product.
- the oil alsofcontains various dissolved sulphonic acid constituents.
- the separated aqueous layer 1 is acidic in nature and contains all of the sulfuric acid constituents and the sludge particles. This acidic aqueous layer also contains someof the sulphonic acid constituents clue tothe fact that these constituents are soluble in acid solutions. However these sulfonic acid constituents arenot soluble in water. As a result these sulfonic constituents are incompletely removed in conventional operations.
- a dilute sulfuric acid solution having a. definite concentration substantially the entire amount of undesirable sulphonic acid constituents are removed with the weak acid solution. These constituents thus are not able to subsequently react with the alkali which cause undesirable emulsions which increase the consumption of the alkali to produce sulphonates.
- the feed oil comprises a cracked distillate boiling in the motor fuel boilin range which contains dissolved therein bjectionable sulfur compounds, as for example mercaptans and related sulfur compounds.
- This oil is introduced into acid treating mixing zone] by means of. feed line 2 in which it is contacted with a suitable acid, which for the purpose of description is taken to'be sulphuric acid.
- The. sulfuric'aci'd is introduced into the system by means of line 3.
- treating zone I may comprise a series of batch units, or may comprise any number of countercurrent'acid treating stages.
- the acid oil is withdrawn from acid treating zone I by means of line 4 and passed serially through settlin'g zones 5 and 6. Acid sludge containing the undesirable sulfur constituents is'withdrawn from the respective units by means of line 1 and 8.
- the acid oil is withdrawn from settling unit 6 by means of line 9 and mixed with a weak acidic so,- lution which-is introduced by'means of line l0.
- The'mixture is passed'to settling zone H from which the weak acid layer, containing dissolved therein sulph'onic acid constituents, is withdrawn by means of line I2.
- the oil layer, completely free of sulphonic acid constituents, is withdrawn from settling zone II by means of line l3 and mixed with a quantity of water, which is introduced by means'of line 14.
- This mixture is introduc'ed :into settle zone I5 from which the water solution containing dissolved therein'sulfuric acid constituents and sludge particles, is removed by mean of line I 6.
- the treated oil is then removed from settling zone l5 b'y'means of line H and completely sweetened by mixing with a neutralizing agent which is taken to be a sodium hydroxide solution which is introduced into the system by means of line l8.
- the mixture is intr'oducedinto settling zone I9 from which the spent sodium hydroxide solution is Withdrawn by means/of line 20, while the treated oil is withdrawn by means of-line 2
- the process of the present invention may be widely varied.
- the invention essentially comprises subjecting an acid treated oil, after removal of the acid sludge, to a weak acid wash prior to removing the treated acid constituents from the same.
- the invention may be applied in the treatment of any petroleum oil which is refined by the treatment of a sulfuric or an equivalent acid such as an acid or phosphorus and the like
- a sulfuric or an equivalent acid such as an acid or phosphorus and the like
- acid concentrations vary in the range from-about 40% to fuming acids and the amount of acid varies in the range from about 1 lb. to about 30 lbs. of acid per barrel of oil being treated.
- the acid oil after separation of the acid sludge is treated with a quantity of weak acid solution which is adjusted in a manner that the acid concentration is in the rangefrom about 0.5 to 3.0% strength, preferably about 1.5 to 2.5% strength.
- the amount of acid remaining in the acid oil will be sufiicient to secure this concentration.
- the acid concentration in the oil will be in the range from about 0.5 to 3.0%.
- the amount of water addedrin the secondary stage is adjusted in a manner to completely remove the sulfuric acid constituents;
- the amount of neutralizing agent likewise is adjusted in order to completely neutralize'all remaining acid constituents.
- Process for the production of a refined oil product from a feed oil containing objectionable sulfur compounds which comprises contacting said feed oil with sulfuric acid under conditions to form an acid sludge containing the objectionable sulfur compounds, separating the acid sludge from the oil, treating the oil in an initial stage with an added dilute sulfuric acid solution having a concentration in the range from about 0.5% to about 3.0%, separating the dilute sulfuric acid solution and. treating the oil in the secondary stage with water, separating the water, contacting the oil in a tertiary stage with an alkali metal hydroxide solution and separating the treated oil product.
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
O'ct- 1943- E. \c. HERMANN 2,332,793
REFINING OF MINERAL OILS Filed NOV. 30, 1940 Patented Oct. 26, 1943 REFININ'G or MINERAIIOILS Eugene C. Hermann, Westfield, N. J assignor to, Standard Oil Developmentcompany, a corporation of Delaware Application November 20, 1940, Serial No. 367,907
The present invention relates to the refining of mineral oils. The invention is more particularly concerned with the refining of petroleum oils boiling in the motor fuel, kerosene, and gas oil boiling ranges, and especially relates to an improved process for the removal of objectionable compounds therefrom, when utilizing as a treating agent a mineral acid such as a sulfuric or an equivalent acid. In accordance with the present process, acid treated oils, after the removal of the acid sludge, are subjected in an initial stage to a weak acid treatment, and then treated in the secondary stage with a washing solution which preferably comprises water. In accordanc with the preferred modification of the invention, the treated oil isthen neutralized with a suitable alkali, as for example an aqueous caustic solution in order to produce an improved refined product. t
It is well known in the art to refine mineral oils, particularly petroleum oils, by various procedures involving distillation, acid treating, clay treating, and neutralization stages. For example, it iswell known in the art to remove objectionable sulfur and related compounds from petroleum oils, particularly from those petroleum oils boiling in the motor fuel boiling range, by "treating the same with suitable mineral acids. The spent acid solution is removed from the oil which is then washed in orderto remove free acidic constituents. The oil after removal of the washing solvent is completely neutralized by treating the same with an alkali metal treating agent such as an aqueous solution of sodium hydroxide. In these operations the mineral acid usually comprises an acid of sulfur, particularly sulfuric acids of various concentrations. The acid jtreating operation is usually conducted under conditions to secure a maximum removal of the objectionable sulfur compounds and a minimum degradation'of the valuable petroleum oil constituents furic acid. However the acid oil does contain,
small quantities of acidic particlesuaswellas .small quantities of sludge particles. In addition,
the oil alsofcontains various dissolved sulphonic acid constituents.
In order to remove these materials it has been the practice to treat the acid oil in one or more stages with a washing solution which usually comprises water. The separated aqueous layer 1 is acidic in nature and contains all of the sulfuric acid constituents and the sludge particles. This acidic aqueous layer also contains someof the sulphonic acid constituents clue tothe fact that these constituents are soluble in acid solutions. However these sulfonic acid constituents arenot soluble in water. As a result these sulfonic constituents are incompletely removed in conventional operations. This results in operating difiiculties since the water washed oil in order to completely free the oil of acid and related harmful constituents, is subsequently neutralized with a suitable alkali which usually comprises an aqueous solution of an alkali metal hydroxide. This operation, while producing a product of high quality entirely suitable for utilization in internal combustion engines and the like, does have the disadvantage that the sul' phonic acid constituents react with the alkali to produce sulphonates, which materials act as emulsifying agents, which produce emulsions which are diflicult to break.
These difficulties cannot be readily overcome sinceif a relatively large quantity of water or equivalent'solvent be utilized for the complete removal of the deleterious sulfuric acid and sludge constituents from the acid oil the resulting solution is relatively weak with respect to its acidity andincomplete removal of the sulfonic acid constituents from the oil results. On the other hand'if a relatively small volume of water is employed for treating the acid oil, the acidity is satisfactory with respect to the solvency of the sulfonic acid constituents but incomplete removal of the sulfuric acid and sludge constituents re sults. Furthermore, when employing-a relatively small volume of water per volume of acid oil an appreciable carry-over of undesirable constituents is experienced.
. Ihave now discovered a process by which it is .possible to remove objectionable sulfur and related compounds from mineral oils utilizing a mineral acid, and to completely neutralize the same in an, efficient andeconomical manner. In
accordance with my process, the mineral or pe initial stage with a definite amount of waterunder conditions in which the oil is subjected to a dilute sulfuric acid solution having a. definite concentration. I have found that if thi operation be conducted, substantially the entire amount of undesirable sulphonic acid constituents are removed with the weak acid solution. These constituents thus are not able to subsequently react with the alkali which cause undesirable emulsions which increase the consumption of the alkali to produce sulphonates. The treated oil, after removal of the weak acid solution, is then subjected in a secondary stage to a treatment with a sumcient quantity of water which is *trations, may vary widely.
able for the refining of petroleum oils boiling in the motor fuel and light gas oil boiling range, with which neutralized sulphonic acid constituents function to produce aqueou emulsions in the neutralization stage. 5
Temperature and pressure conditions of the acid treating operation, as well as acid concen- In general, atmospheric temperatures and pressures are employed,
adjusted to substantially completely remove the remaining sulphuric acid constituents. This oil is then removed and completely neutralized by treatment with a suitable alkali metal hydroxide solution to produce a finished product having'an exceptionally high quality. A,
The process of my invention may be readily understood by reference to the attached drawing illustrating modifications of the same. For purposes of description it is assumed that the feed oil comprises a cracked distillate boiling in the motor fuel boilin range which contains dissolved therein bjectionable sulfur compounds, as for example mercaptans and related sulfur compounds. This oil is introduced into acid treating mixing zone] by means of. feed line 2 in which it is contacted witha suitable acid, which for the purpose of description is taken to'be sulphuric acid. The. sulfuric'aci'd is introduced into the system by means of line 3. It is to be understood that treating zone I may comprise a series of batch units, or may comprise any number of countercurrent'acid treating stages. The acid oil is withdrawn from acid treating zone I by means of line 4 and passed serially through settlin'g zones 5 and 6. Acid sludge containing the undesirable sulfur constituents is'withdrawn from the respective units by means of line 1 and 8. The acid oil is withdrawn from settling unit 6 by means of line 9 and mixed with a weak acidic so,- lution which-is introduced by'means of line l0. The'mixture is passed'to settling zone H from which the weak acid layer, containing dissolved therein sulph'onic acid constituents, is withdrawn by means of line I2. The oil layer, completely free of sulphonic acid constituents, is withdrawn from settling zone II by means of line l3 and mixed with a quantity of water, which is introduced by means'of line 14. This mixture is introduc'ed :into settle zone I5 from which the water solution containing dissolved therein'sulfuric acid constituents and sludge particles, is removed by mean of line I 6. The treated oil is then removed from settling zone l5 b'y'means of line H and completely sweetened by mixing with a neutralizing agent which is taken to be a sodium hydroxide solution which is introduced into the system by means of line l8. The mixture is intr'oducedinto settling zone I9 from which the spent sodium hydroxide solution is Withdrawn by means/of line 20, while the treated oil is withdrawn by means of-line 2|.
The process of the present invention may be widely varied. The invention essentially comprises subjecting an acid treated oil, after removal of the acid sludge, to a weak acid wash prior to removing the treated acid constituents from the same. I
The invention may be applied in the treatment of any petroleum oil which is refined by the treatment of a sulfuric or an equivalent acid such as an acid or phosphorus and the like However,
although temperatures in the range below 40 F. to F. andthe' like are also suitable. The acid concentration will depend upon the particular acid'us'ed, the quantity of acid used, th type of feed oil being treated, and the character and con centration of the undesirable sulfur compounds.
In general acid concentrations vary in the range from-about 40% to fuming acids and the amount of acid varies in the range from about 1 lb. to about 30 lbs. of acid per barrel of oil being treated.
The acid oil after separation of the acid sludge is treated with a quantity of weak acid solution which is adjusted in a manner that the acid concentration is in the rangefrom about 0.5 to 3.0% strength, preferably about 1.5 to 2.5% strength. Under certain conditions, providing thequan'tity of water added to the initial stage be relatively low, the amount of acid remaining in the acid oil will be sufiicient to secure this concentration. For example, we have discovered that when treat ing a petroleum oil boiling in the motor fuel boiling range with 5 to 15 lbs. of to 98% of sulfuric acid if l to 5 volumes of water per volume of oil be added in the initial stage, the acid concentration in the oil will be in the range from about 0.5 to 3.0%. g'
The amount of water addedrin the secondary stage is adjusted in a manner to completely remove the sulfuric acid constituents; The amount of neutralizing agent likewise is adjusted in order to completely neutralize'all remaining acid constituents. 1
In order to further illustrate the invention, the following example is given which should not be construed as limiting the same in any manner whatsoever.
Example Various operations were conducted to determine the solubility of sulphonic acids with the following results: I
. Per cent water in mix of 8.6 10.2 15.9.
oil and Water. Methyl orange acidity of 12.2 8.7 6.9.
water phase as cc.s of N/10/5 cc.'s. Nature of water phasc Sulphonic V e r y Incomplete acids well slightly solution of dissolved. murky. sulphonic acids. Sp. gr. of water phase".-. 1.0233 l.0l98 1.0165.
about 3.0% in an initial stage, separating the oil from the dilute acid solution and washing the oil in a secondary stage with water.
2. Process in accordance with claim 1 in which said mineral oil is a petroleum oil boiling in the motor fuel boiling range. a
3. Process for the production of a refined oil product from a feed oil containing objectionable sulfur compounds which comprises contacting said feed oil with sulfuric acid under conditions to form an acid sludge containing the objectionable sulfur compounds, separating the acid sludge from the oil, treating the oil in an initial stage with an added dilute sulfuric acid solution having a concentration in the range from about 0.5% to about 3.0%, separating the dilute sulfuric acid solution and. treating the oil in the secondary stage with water, separating the water, contacting the oil in a tertiary stage with an alkali metal hydroxide solution and separating the treated oil product.
4. Process in accordance with claim 3 in which said petroleum oil boils in the motor fuel boiling range.
EUGENE C. HERMANN.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US367907A US2332793A (en) | 1940-11-30 | 1940-11-30 | Refining of mineral oils |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US367907A US2332793A (en) | 1940-11-30 | 1940-11-30 | Refining of mineral oils |
Publications (1)
Publication Number | Publication Date |
---|---|
US2332793A true US2332793A (en) | 1943-10-26 |
Family
ID=23449103
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US367907A Expired - Lifetime US2332793A (en) | 1940-11-30 | 1940-11-30 | Refining of mineral oils |
Country Status (1)
Country | Link |
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US (1) | US2332793A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2769770A (en) * | 1952-06-14 | 1956-11-06 | Universal Oil Prod Co | Removing arsenic from a naphtha, which is reformed with a noble metal catalyst composite |
US3027318A (en) * | 1962-03-27 | Purification of crude coke |
-
1940
- 1940-11-30 US US367907A patent/US2332793A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3027318A (en) * | 1962-03-27 | Purification of crude coke | ||
US2769770A (en) * | 1952-06-14 | 1956-11-06 | Universal Oil Prod Co | Removing arsenic from a naphtha, which is reformed with a noble metal catalyst composite |
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