US2088406A - Process of refining mineral oil - Google Patents
Process of refining mineral oil Download PDFInfo
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- US2088406A US2088406A US6189A US618935A US2088406A US 2088406 A US2088406 A US 2088406A US 6189 A US6189 A US 6189A US 618935 A US618935 A US 618935A US 2088406 A US2088406 A US 2088406A
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- oil
- acid
- per cent
- refined
- mixture
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- 238000000034 method Methods 0.000 title description 20
- 239000002480 mineral oil Substances 0.000 title description 19
- 235000010446 mineral oil Nutrition 0.000 title description 14
- 238000007670 refining Methods 0.000 title description 14
- 239000003921 oil Substances 0.000 description 63
- 239000000203 mixture Substances 0.000 description 27
- 239000002253 acid Substances 0.000 description 26
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 24
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 21
- 239000001117 sulphuric acid Substances 0.000 description 21
- 235000011149 sulphuric acid Nutrition 0.000 description 21
- 239000010802 sludge Substances 0.000 description 14
- 235000011007 phosphoric acid Nutrition 0.000 description 13
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 10
- 229960004838 phosphoric acid Drugs 0.000 description 10
- 239000010779 crude oil Substances 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- 125000001931 aliphatic group Chemical group 0.000 description 7
- 239000003153 chemical reaction reagent Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001491 aromatic compounds Chemical class 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- ZXPNHQOWDWPUEH-UHFFFAOYSA-N boric acid;sulfuric acid Chemical compound OB(O)O.OS(O)(=O)=O ZXPNHQOWDWPUEH-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- -1 olefin compounds Chemical class 0.000 description 2
- YXJYBPXSEKMEEJ-UHFFFAOYSA-N phosphoric acid;sulfuric acid Chemical compound OP(O)(O)=O.OS(O)(=O)=O YXJYBPXSEKMEEJ-UHFFFAOYSA-N 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910000286 fullers earth Inorganic materials 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000011221 initial treatment Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 230000000630 rising effect Effects 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
- Crude mineral oils and especially those of the naphthemc type which are obtained from the Gulf coast and mid-continental petroleum fields contain a high percentage of both unsaturated aliphatic and unsaturated aromatic hydrocarbons.
- the formation in mineral oil during use of insoluble gummy and resinous masses (commonly called sludge), and the instability of mineral oil when subjected to heat and exposed to air and light is to be ascribed to the presence in the oil of these unsaturated compounds. It has been the object of refining processes to remove unsaturated compounds as completely as possible.
- Oils of this type although not subject to sludge formation, are easily oxidized on exposure to air and soluble products which are highly acidic and corrosive in nature are formed.
- the acid products form permanent emulsions with the oil and water which may be present. Water may be formed by oxida-, tion or may enter the transformer during. operation.
- Such emulsions hasten electrical breakdown.
- Under-refined oils and over-refined oils because of the formation of sludge and acid products respectively likewise have been found unsuited for other electrical application, for example, as cooling or dielectric media in cables and capacitors.
- An'acid mixture containing the proper amounts of sulphuric acid and phosphoric acid attacks the olefinic constituents preferentially, resulting in a product which contains the minimum of olefinic unsaturation and the desired amount of unsaturated aromatic compounds.
- Fig. 1 of the accompanying drawing graphs are represented showing the relation of sludge formation when crude mineral oils were treated with varying amounts of diiferent refining agents.
- Fig. 2 are represented graphs showing the rate of sludge accumulation in crude oil and in oil refined by various methods.
- the oil is treated with a mixture of sulphuric acid and phosphoric acid
- the procedure preferred is as follows: 5 pounds of an acid mixture composed of approximately per cent commercially concentrated sulphuric acid (for example, sp. gr. 1.84, 96% strength) and approximately 15 per cent crthophosphoric acid (for example, sp. gr. 1.71, 85% strength) is added slowly with continuous agitation to 55 gallons of crude mineral oil.
- the rate of addition is such that the temperature will not rise higher than about 35 C.
- the temperature of the oil-acid mixture should be kept below 25 C.
- the oil-acid mixture is allowed to stand until the resulting sludge is settled out.
- the unsaturated aromatic compounds stabilize the oil against oxidation and sludge formation, reduce to a minimum the soluble acidic products of oxidation, and stabilize the oil against ionization effects when subjected to electric stress which is capable of causing a splitting oil of hydrogen and the polymerization of the hydrocarbon residue with the formation of insoluble waxy materials.
- Fig. 2 represents by difierent graphs the percentage of sludge by weight formed during a given time with different refining agents using an optimum amount as indicated in Fig. 1.
- Graph D represents the sludging characteristics of crude oil
- graph E represents that of oil purified by sulphuric acid (15 lbs. sulphuric acid per 55 gallons of oil)
- graph F represents that of oil purified by a sulphuric acid-boric acid mixture (10 lbs. acid mixture containing 2.7% boric acid per 55 gallons of oil)
- graph G represents the sludging characteristics of oil purified by a sulphuric acidphosphoric acid mixture (5 lbs. acid mixture containing 15% phosphoric acid per 55 gallons of oil).
- Crude oil refined by the sulphuric acidphosphoric acid mixture exhibits superior nonsludging characteristics although smaller amounts of the refining agent were employed.
- the following method was used to determine the sludging characteristics of the various oils represented in the graphsof Figs. 1 and 2.
- 55 cc. of the'oil were placed in a Pyrex test tube containing a copper spiral and heated in an oven at C.
- the test tubes were removed at definite intervals, the oxidized oil was diluted with an equal amount of naphtha and then was centrifuged.
- the sludge obtained was washed by repeated naphtha additions and centrifuged until free from oil, after which the weight of the sludge was determined gravimetrically and expressed in per cent by weight of the original oil.
- crude mineral oil as used herein I mean a non-refined or a semi-refined oil stock which, when treated as herein described, is adapted for use in an electrical insulating or dielectric capacity.
- a method of treating crude mineral oil which comprises agitating the oil at a temperature not substantially exceeding 35 C. with a reagent consisting of about 85. per cent concentrated sulphuric acid and about 15 per cent concentrated phosphoric acid.
- a process of treating crude mineral oil which comprises agitating said oil with a reagent consisting of about 85 per cent concentrated sulphuric acid and about 15 per cent phosphoric acid of about 85 per cent acid strength, said reagent being applied to said oil in the ratio of about 4 to 15 pounds of reagent to about 55 gallons of oil, and suppressing substantial rise in temperature.
- a process of treating crude mineral oil which comprises agitating said oil with a reagent consisting of about 85 per cent concentrated sulphuric acid and about 15 per cent phosphoric acid of about 85 per cent acid strength, said reagent being applied to said oil in the ratio of about 5 pounds of reagent to about 55 gallons of oil, and. preventing the temperature from rising above about 35 C.
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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)
- Organic Insulating Materials (AREA)
Description
July 27, 1937.
Fig.
Fig.2.
F. M. CLARK 2,088,405 PROCESS OE'REFINING MINERAL OIL original Filed May l9, 1934 r A320 Was/yr T/ME IN DflYS Inventor:
Frank M. Clark,
His Attorney.
Patented July 27 1937 rnoonss 0F REFINING MINERAL OIL Frank M. Clark, Pittsfield, Mass, assignor to General Electric Company, a corporation of New York Original application May 19, 1934, Serial No. 726,498. Divided and this application February 12, 1935, Serial No. 6,
6 Claims.
The present invention comprises an improved method of refining mineral oil compositions with the main object in view of producing an oil which is particularly well suited for insulating and dielectric purposes. This application is a division of my prior application Serial No. 726,498, filed May 19, 1934.
Crude mineral oils and especially those of the naphthemc type which are obtained from the Gulf coast and mid-continental petroleum fields contain a high percentage of both unsaturated aliphatic and unsaturated aromatic hydrocarbons. The formation in mineral oil during use of insoluble gummy and resinous masses (commonly called sludge), and the instability of mineral oil when subjected to heat and exposed to air and light is to be ascribed to the presence in the oil of these unsaturated compounds. It has been the object of refining processes to remove unsaturated compounds as completely as possible.
Heretoiore the general practice in the refining of mineral oils has involved initial treatment at high temperatures with concentrated (or fuming) sulphuric acid or else with phosphoric acid. It has also been proposed to associate the sulphuric acid with boric acid.
Although these prior methods are of value in the treatment of certain types of oils, they all possess certain disadvantages. Mineral oils treated in accordance with the previously proposed methods are apt to be either under-refined or over-refined and hence not well suited for use in an insulating or dielectric capacity. For example, under-refined oils contain unsaturated aliphatic hydrocarbons, such as olefin compounds, which by oxidation and polymerization form sludge. When under-refined oil is used in transformers, any sludge which may be formed obstructs the circulation of the oil and reduces the desired cooling effect. A transformer in this condition is easily overheated and caused to fail. Over-refined oils on the other hand contain. substantially no unsaturated compounds. Oils of this type, although not subject to sludge formation, are easily oxidized on exposure to air and soluble products which are highly acidic and corrosive in nature are formed. When such oil is used in a transformer the acid products form permanent emulsions with the oil and water which may be present. Water may be formed by oxida-, tion or may enter the transformer during. operation. Such emulsions hasten electrical breakdown. Under-refined oils and over-refined oils because of the formation of sludge and acid products respectively likewise have been found unsuited for other electrical application, for example, as cooling or dielectric media in cables and capacitors.
When crude oils are refined by treatment with concentrated sulphuric acid alone both aliphatic and aromatic unsaturated compounds are removed. As the sulphuric acid combines with the aliphatic and aromatic unsaturated bodies equal- 1y well, it isvimpossible to remove one type of unsaturated compounds without also removing the other. Transformer oil in use today refined by the sulphuric acid process is a compromise oil. It contains both the sludge-forming and acidproducing compounds. Oils treated with phosphoric acid are subject to practically the same disadvantage. When the sulphuric acid is associated with boric acid the unsaturated aromatic component of the oil is less attacked but likewise the effect of the sulphuric acid on the aliphatic unsaturated components is reduced. As is well known, transformer and other oils used in an insulating and dielectric capacity commonly have a Saybolt universal viscosity at F. not over about 200 seconds, for example, between about 60 and seconds.
In accordance with my present invention I have provided a method of producing a mineral oil which is particularly Well suited for electrical insulating and dielectric purposes. The product resulting from the herein described refining treatment contains less, than one per cent by volume of olefinic (aliphatic) hydrocarbons and about 4 to 8 per cent by. volume of residual unsaturated aromatic hydrocarbons.
In accordance with my invention I have provided a process for purifying and refining crude mineral oilsto produce my improved oil product by the treatment of the crude oil with an acid mixture composed preponderantly of sulphuric acid andcontaining a minor proportion of phosphoric'acid. An'acid mixture containing the proper amounts of sulphuric acid and phosphoric acid attacks the olefinic constituents preferentially, resulting in a product which contains the minimum of olefinic unsaturation and the desired amount of unsaturated aromatic compounds. I
The oil resulting from this treatment is stable, and is particularly adapted for insulating and dielectric purposes. It contains less than one per cent by volume of olefinic (aliphatic) hydrocarbons and about 4 to-8 per cent by volume of unsaturated aromatichydrocarbons.
In Fig. 1 of the accompanying drawing, graphs are represented showing the relation of sludge formation when crude mineral oils were treated with varying amounts of diiferent refining agents. In Fig. 2 are represented graphs showing the rate of sludge accumulation in crude oil and in oil refined by various methods.
When in accordance with my invention the oil is treated with a mixture of sulphuric acid and phosphoric acid, the procedure preferred is as follows: 5 pounds of an acid mixture composed of approximately per cent commercially concentrated sulphuric acid (for example, sp. gr. 1.84, 96% strength) and approximately 15 per cent crthophosphoric acid (for example, sp. gr. 1.71, 85% strength) is added slowly with continuous agitation to 55 gallons of crude mineral oil. The rate of addition is such that the temperature will not rise higher than about 35 C. Preferably the temperature of the oil-acid mixture should be kept below 25 C. The oil-acid mixture is allowed to stand until the resulting sludge is settled out. The supernatant refined oil is separated, Washed with water or with a weak alkaline solution in order to neutralize any free acids left in the oil. A 3 per cent sodium hydroxide solution is preferred for the alkaline wash. Weaker or stronger solutions may be used although the alkaline solution should not be higher than 5 per cent in concentration. The refined oil is dehydrated and then may be subjected to a fullers earth treatment, although the latter treatment is not indispensable.
The oil treated by a properly balanced refining acid mixture as above described is extremely stable and is neither under-refined nor over-refined. An oil which is especially suited for insulating application shows an aliphatic (olefinic) unsaturation of less than 1 per cent and a much larger amount of unsaturated aromatic compounds ranging from 4 to 8 per cent.
The unsaturated aromatic compounds stabilize the oil against oxidation and sludge formation, reduce to a minimum the soluble acidic products of oxidation, and stabilize the oil against ionization effects when subjected to electric stress which is capable of causing a splitting oil of hydrogen and the polymerization of the hydrocarbon residue with the formation of insoluble waxy materials.
In Figure 1 of the drawing, graph A represents characteristics of oil treated with sulphuric acid, graph B represents characteristics of oil treated with the sulphuric acid-boric acid mixture and graph C represents characteristics of oil treated with the sulphuric acid-phosphoric acid mixture in accordance with my invention. The percentage of sludge by weight accumulated on the 35th day was determined and plotted as ordinates, the amount of refining agent being plotted as abscissae. As shown by graph A increased amounts of sulphuric acid produced oil having correspondingly lower sludging characteristics. The best results for the sulphuric acid-boric acid mixture (graph B) were obtained when 10 lbs. of the acid mixture (containing 2.7% boric acid) were used with 55 gallons of crude oil. As shown by the graph C oil refined by treatment with the sulphuric acid-phosphoricacid mixture (containing 15% phosphoric acid) resulted in an oil having lower sludging characteristics than oil refined by either of the other two methods. The best results as shown by this graph were obtained using 5 lbs. of the sulphuric phosphoric acids mixture per 55 gallons of crude oil but, as shown in Fig. 1, effective results are alsolobtained when the oil is treated with the sulphuric-phosphoric acidsmixture in the ratio of about 4 to 15 lbs. of said mixture per 55 gallons of crude oil.
Fig. 2 represents by difierent graphs the percentage of sludge by weight formed during a given time with different refining agents using an optimum amount as indicated in Fig. 1. ,Graph D represents the sludging characteristics of crude oil, graph E represents that of oil purified by sulphuric acid (15 lbs. sulphuric acid per 55 gallons of oil), graph F represents that of oil purified by a sulphuric acid-boric acid mixture (10 lbs. acid mixture containing 2.7% boric acid per 55 gallons of oil), and graph G represents the sludging characteristics of oil purified by a sulphuric acidphosphoric acid mixture (5 lbs. acid mixture containing 15% phosphoric acid per 55 gallons of oil). Crude oil refined by the sulphuric acidphosphoric acid mixture exhibits superior nonsludging characteristics although smaller amounts of the refining agent were employed.
The following method was used to determine the sludging characteristics of the various oils represented in the graphsof Figs. 1 and 2. 55 cc. of the'oil were placed in a Pyrex test tube containing a copper spiral and heated in an oven at C. The test tubes were removed at definite intervals, the oxidized oil was diluted with an equal amount of naphtha and then was centrifuged. The sludge obtained was washed by repeated naphtha additions and centrifuged until free from oil, after which the weight of the sludge was determined gravimetrically and expressed in per cent by weight of the original oil.
By the term crude mineral oil as used herein I mean a non-refined or a semi-refined oil stock which, when treated as herein described, is adapted for use in an electrical insulating or dielectric capacity.
Although I have described my invention setting forth the purification and refinement of crude mineral oils in general using specific proportions of my acid mixture, it will be understood by those skilled in the art that some types of crude. oils may require modifications in the acid ratio. All modifications of my process coming within the true spirit and scope of my invention are meant to be covered in the appended claims.
What I claim as new and desire to secure by Letters Patent of the United States is:
1. A method of refining crude mineral oil which comprises treating the oil at a temperature not substantially exceeding 35 C. with a mixture comprising approximately 85 per cent concentrated sulphuric acid and approximately 15 per cent concentrated phosphoric acid, and removing acidic compounds and uncombined acid.
2. A method of treating crude mineral oil which comprises agitating the oil at a temperature not substantially exceeding 35 C. with a reagent consisting of about 85. per cent concentrated sulphuric acid and about 15 per cent concentrated phosphoric acid.
'3. The method of treating crude mineral oil preparatory to its use for electrical insulating and dielectric purposes which consists in bringing such oil into contact with a mixture of approximately 85 per cent'concentrated sulphuric acid and approximately 15 percent concentrated orthophosphoric acid at a temperature below about '35" C., allowing the-mixture to stand until the resulting sludge settles, removing the supernatant oil and removing acid'and water therefrom.
4. A process of treating crude mineral oil which comprises agitating said oil with a reagent consisting of about 85 per cent concentrated sulphuric acid and about 15 per cent phosphoric acid of about 85 per cent acid strength, said reagent being applied to said oil in the ratio of about 4 to 15 pounds of reagent to about 55 gallons of oil, and suppressing substantial rise in temperature.
5. A process of treating crude mineral oil which comprises agitating said oil with a reagent consisting of about 85 per cent concentrated sulphuric acid and about 15 per cent phosphoric acid of about 85 per cent acid strength, said reagent being applied to said oil in the ratio of about 5 pounds of reagent to about 55 gallons of oil, and. preventing the temperature from rising above about 35 C.
6. The step in a process of refining crude mineral oil for electrical application which comprises treating said oil with an acid mixture consisting of about 85 per cent concentrated sulphuric acid and about 15 per cent orthophosphoric acid of about 85 per cent acid strength, said acid mixture being applied to said oil in the ratio of about 5 pounds of acid mixture to about 55 gallons of oil.
FRANK M. CLARK.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6189A US2088406A (en) | 1934-05-19 | 1935-02-12 | Process of refining mineral oil |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US726498A US2112735A (en) | 1934-05-19 | 1934-05-19 | Mineral oil product |
| US6189A US2088406A (en) | 1934-05-19 | 1935-02-12 | Process of refining mineral oil |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2088406A true US2088406A (en) | 1937-07-27 |
Family
ID=26675300
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US6189A Expired - Lifetime US2088406A (en) | 1934-05-19 | 1935-02-12 | Process of refining mineral oil |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2088406A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2508038A (en) * | 1947-06-13 | 1950-05-16 | Shell Dev | Process of refining hydrocarbons |
-
1935
- 1935-02-12 US US6189A patent/US2088406A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2508038A (en) * | 1947-06-13 | 1950-05-16 | Shell Dev | Process of refining hydrocarbons |
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