US2959539A - Balanced alkali-acid stabilization of fuel oils - Google Patents
Balanced alkali-acid stabilization of fuel oils Download PDFInfo
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- US2959539A US2959539A US593785A US59378556A US2959539A US 2959539 A US2959539 A US 2959539A US 593785 A US593785 A US 593785A US 59378556 A US59378556 A US 59378556A US 2959539 A US2959539 A US 2959539A
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- alkali metal
- oil
- metal hydroxide
- acid
- treated
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- 239000002253 acid Substances 0.000 title claims description 37
- 239000000295 fuel oil Substances 0.000 title description 6
- 230000006641 stabilisation Effects 0.000 title description 2
- 238000011105 stabilization Methods 0.000 title description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 29
- 239000003208 petroleum Substances 0.000 claims description 21
- 150000003839 salts Chemical class 0.000 claims description 20
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 18
- 239000010802 sludge Substances 0.000 claims description 17
- 229910052783 alkali metal Inorganic materials 0.000 claims description 12
- 239000000446 fuel Substances 0.000 claims description 12
- -1 HYDROGEN ATOMS Chemical group 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 11
- 238000009835 boiling Methods 0.000 claims description 10
- 239000003502 gasoline Substances 0.000 claims description 9
- 230000002378 acidificating effect Effects 0.000 claims description 8
- 150000001340 alkali metals Chemical class 0.000 claims description 6
- 239000000470 constituent Substances 0.000 claims description 5
- 239000013049 sediment Substances 0.000 claims description 5
- 239000003921 oil Substances 0.000 description 31
- 239000000243 solution Substances 0.000 description 19
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 11
- 230000007935 neutral effect Effects 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000003518 caustics Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 6
- 239000011368 organic material Substances 0.000 description 5
- 239000002699 waste material Substances 0.000 description 5
- 230000029936 alkylation Effects 0.000 description 4
- 238000005804 alkylation reaction Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000006386 neutralization reaction Methods 0.000 description 4
- 230000003472 neutralizing effect Effects 0.000 description 4
- 150000007530 organic bases Chemical class 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000010771 distillate fuel oil Substances 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 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
- 239000010743 number 2 fuel oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical class [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 125000003396 thiol group Chemical class [H]S* 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- 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
Definitions
- treatment with strong sulfuric acid not only leads to high losses of oil but also presents a waste disposal problem in the acid sludge.
- Caustic treatment even with regeneration presents the problem of disposal of the mixture of phenols and thiophenols together with other organic compounds which are extracted by the caustic solution.
- the present process provides a means whereby treated fuel oils of improved stability can be produced and the only product to be disposed to waste is an aqueous solution of neutral inorganic salts.
- the present process provides for iirst contacting the distillate fuel fraction or other like petroleum fraction boiling above the gasoline range at a temperatnre of about 70 to 180 F. with a solution of strong alkali metal hydroxide of at least 35 weight percent concentration in one or more treating stages at an oil to treating solution ratio of about 4:1 to 30:1.
- the mixture of oil and treating solution is stratied and forms three phases,an upper layer of partially treated oil, an intermediate layer or phase comprising alkali metal salts of the acidic materials present in the charge stock and including alkali metal salts of alkyl phenols or cresols, and alkali metal salts of sulfhydryls including thiophenols, and a bottom layer or phase comprising alkali metal hydroxide solution.
- alkali metal hydroxide concentrations of 35 weight percent or greater the alkali metal salts of the acidic organic material can be separated from the aqueous alkali metal hydroxide solution. Accordingly, the partially treated oil is separated from the other two layers, the organic salt layer is separated from the alkali metal hydroxide solution and the alkali metal hydroxide solution returned to the treating stage.
- the partially treated oil is then mixed With an acid having a free acidity at least equal to about 90 percent '2,959,539' Patented Nov. 8, 19760 Weight sulfuric acid.
- This provides a means for solving the problem of the disposal of spent alkylation sulfuric acid containing at least Weight percent sulfuric acid and other waste acids of similar strength. However, fresh 90 percent or stronger acids can be used.
- the mixture of partially treated oil and acid is stratified to provide an upper layer of twice treated oil and a lower layer of acid sludge.
- the twice treated oil is separated from the acid sludge.
- the twice treated oil is then Washed with dilute aqueous alkali metal hydroxide solution containing about l0 to about 20, preferably about 15, Weight percent alkali metal hydroxide.
- the mixture of twice treated oil and dilute aqueous alkali metal hydroxide solution is stratified and the neutralized twice treated oil separated from the dilute aqueous alkali metal hydroxide solution.
- the neutralized twice treated oil is then water washed and separated from the Wash water to provide a treated oil of improved stability with respect 'to at least one of color and sediment.
- the amounts of strong alkali metal hydroxide, i.e., 4050 Baume aqueous sodium hydroxide or potassium hydroxide, of strong acid, e.g., 92-98 weight percent spent sulfuric acid alkylation acid or fresh acid, and dilute, eg. 10-20 weight percent, aqueous sodium or potassium hydroxide employed are such that when the organic salt layer is mixed with acid layer from the acid treat and with aqueous layer from the neutralization step the organic acids and organic bases will be set free, i.e., sprung, and the aqueous solution sen-t to waste will be a substantially neutral solution of inorganic salts, e.g., sodium and/ or potassium sulfates.
- a catalytically cracked No. 2 fuel oil (domestic heating oil having a boiling range of 400 F. to 650 F.) was contacted at 110 F. with 5 volume percent of 50 Baume potassium hydroxide. ratio 20:1.)
- the partiallyl treated oil was separated from the organic salt layer and the aqueous potassium hydroxide layer.
- the partially treated or caustic treated oil was then contacted at F. with 0.4 pound per barrel of caustic treated oil of 93 weight percent spent sulfuric acid alkylation acid.
- the caustic-treated, acid-treated, or twice treated, oil was separated from the acid sludge.
- the twice treated oil was then neutralized with dilute sodium hydroxide, e.g., 15 weight percent aqueous sodium hydroxide.
- the neutralized oil was separated from the aqueous phase and water washed.
- the amount of acid' in the acid sludge is in excess of the amount required to spring the organic constituents from the. organic salt layer but that the amount of free alkali metal hydroxide in the aqueous layer from the neutralization step is suicient to yield a neutral eiuent. Therefore, the amount of sludgev mixed with the organic salt layer is sufficient to provide enough acid ions to react with all ⁇ of the alkali metal in the organic salt layer in accordance with, the equation and the amount of free alkali metal hydroxide in the aqueous layer from the neutralizing step is suicient to neutralize the mixture of organic salt layer and acid sludge.
- a fuel oil of improved stability with respect to color and sediment and at the same time the problem of ⁇ disposing of the organic salt layer and the acid sludge is eliminated.
- the free organic acids, i.e., phenols, etc. and the free organic bases from the acid sludge can be recovered or used as a source of fuel, or used as a ⁇ component of industrial fuels.
- the substantially neutral aqueous solution of neutral salts presents no pollution problem and can be discharged to any sewer or water course.
- aqueous alkaliA metal hydroxide immediately contacting said partially treated oil with a solution containing at ⁇ least weight percent sulfuric acid to obtain twicetreated petroleum fraction and acid sludge; separating twice-treated petroleum fraction from acid sludge; immediately contacting twice-treated petroleum fraction with suicient aqueous alkali metal hydroxide to produce neutralized twice-treated oil; separating neutralized twicetreated oil from aqueous alkali ⁇ metal ⁇ hydroxide; waterwashing said neutralizedV twice-treated petroleum fraction to, produce water-washed, neutralized, twice-treated petroleum fraction; and separating water-washed, neutralized, twice-treated petroleum fraction from washwater, the improvement that comprises mixing the aforesaid alkali metal salts of organic constituents having replaceable acidic hydrogen atoms, 4said acid sludge and said aqueous alkali metal hydroxide from the neutralization of said twice-treated oil in proportions such that a neutral aqueous layer separates from a layer of organic material including said
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Nov. 8, 1960 c. A. DUVAL, JR
BALANCED ALKALI-ACID ST-ABILIZATIN OF FUEL OILS Filed June 25, 1956 @SSG bmw SS QEE -S S United States Patent O M'ce BALANCED ALKALI-ACID STABILIZATION OF FUEL OILS Claiborne A. Duval, Jr., Beaumont, Tex., assignor to Socony Mobil Oil Company, Inc., New York, N.Y., a corporation of New York Filed June 25, 1956, Ser. No. 593,785
6 Claims. (Cl. 208-271) 'Ihe present invention relates to the treatment of petroleum fuel fractions boiling higher than gasoline and, more particularly, to the treatment of distillate fuel oils to produce a distillate fuel oil stable to at least one of color and sediment.
It is well known that the stability of petroleum fuel fractions boiling above the gasoline range can be improved by acid treating, caustic treating, hydrogenation, vapor phase refining or furfural treating. These processes are in some instances costly, in other instances yield products of lower than desired quality or produce waste disposal problems.
Thus, treatment with strong sulfuric acid not only leads to high losses of oil but also presents a waste disposal problem in the acid sludge. Caustic treatment even with regeneration presents the problem of disposal of the mixture of phenols and thiophenols together with other organic compounds which are extracted by the caustic solution.
The present process provides a means whereby treated fuel oils of improved stability can be produced and the only product to be disposed to waste is an aqueous solution of neutral inorganic salts.
Broadly stated, the present process provides for iirst contacting the distillate fuel fraction or other like petroleum fraction boiling above the gasoline range at a temperatnre of about 70 to 180 F. with a solution of strong alkali metal hydroxide of at least 35 weight percent concentration in one or more treating stages at an oil to treating solution ratio of about 4:1 to 30:1. The mixture of oil and treating solution is stratied and forms three phases,an upper layer of partially treated oil, an intermediate layer or phase comprising alkali metal salts of the acidic materials present in the charge stock and including alkali metal salts of alkyl phenols or cresols, and alkali metal salts of sulfhydryls including thiophenols, and a bottom layer or phase comprising alkali metal hydroxide solution. At alkali metal hydroxide concentrations of 35 weight percent or greater the alkali metal salts of the acidic organic material can be separated from the aqueous alkali metal hydroxide solution. Accordingly, the partially treated oil is separated from the other two layers, the organic salt layer is separated from the alkali metal hydroxide solution and the alkali metal hydroxide solution returned to the treating stage.
It is Well known that the reaction between an acidic material such as a phenol and an alkali metal hydroxide produces water of reaction at the rate of one mol of water for each acidic hydrogen ion replaced by an alkali metal ion. Consequently, the whole or a part of the separated alkali metal hydroxide solution is concentrated by evaporation of the water so that when mixed with the unconcentrated portion of the separated alkali metal hydroxide solution the resulting caustic solution will have a concentration of at least 35 weight percent alkali metal hydroxide.
The partially treated oil is then mixed With an acid having a free acidity at least equal to about 90 percent '2,959,539' Patented Nov. 8, 19760 Weight sulfuric acid. This provides a means for solving the problem of the disposal of spent alkylation sulfuric acid containing at least Weight percent sulfuric acid and other waste acids of similar strength. However, fresh 90 percent or stronger acids can be used.
The mixture of partially treated oil and acid is stratified to provide an upper layer of twice treated oil and a lower layer of acid sludge. The twice treated oil is separated from the acid sludge. The twice treated oil is then Washed with dilute aqueous alkali metal hydroxide solution containing about l0 to about 20, preferably about 15, Weight percent alkali metal hydroxide. The mixture of twice treated oil and dilute aqueous alkali metal hydroxide solution is stratified and the neutralized twice treated oil separated from the dilute aqueous alkali metal hydroxide solution. The neutralized twice treated oil is then water washed and separated from the Wash water to provide a treated oil of improved stability with respect 'to at least one of color and sediment.
It is to be emphasized that the amounts of strong alkali metal hydroxide, i.e., 4050 Baume aqueous sodium hydroxide or potassium hydroxide, of strong acid, e.g., 92-98 weight percent spent sulfuric acid alkylation acid or fresh acid, and dilute, eg. 10-20 weight percent, aqueous sodium or potassium hydroxide employed are such that when the organic salt layer is mixed with acid layer from the acid treat and with aqueous layer from the neutralization step the organic acids and organic bases will be set free, i.e., sprung, and the aqueous solution sen-t to waste will be a substantially neutral solution of inorganic salts, e.g., sodium and/ or potassium sulfates.
Thus, for example, a catalytically cracked No. 2 fuel oil (domestic heating oil having a boiling range of 400 F. to 650 F.) was contacted at 110 F. with 5 volume percent of 50 Baume potassium hydroxide. ratio 20:1.) The partiallyl treated oil was separated from the organic salt layer and the aqueous potassium hydroxide layer. The partially treated or caustic treated oil was then contacted at F. with 0.4 pound per barrel of caustic treated oil of 93 weight percent spent sulfuric acid alkylation acid. The caustic-treated, acid-treated, or twice treated, oil was separated from the acid sludge.
lThe twice treated oil was then neutralized with dilute sodium hydroxide, e.g., 15 weight percent aqueous sodium hydroxide. The neutralized oil was separated from the aqueous phase and water washed.
The organic salt layer from the strong caustic treat, the acid sludge from the acid treat and the aqueous phase from the neutralizing treat were mixed.v A layer ofl or-` ganic material including phenols, carboxylic acids, thiophenols, and organic bases together with some entrained oil was separated from an aqueous solution of inorganic salts, i.e., sulfates which was substantially neutral. The results of this caustic-acid treatment of the aforesaid fuel oil are presented in the following tabulation:
1 Held in a. glass bottle for 12 Weeks at 110 F.
(Treating It will be noted that the amount of acid' in the acid sludge is in excess of the amount required to spring the organic constituents from the. organic salt layer but that the amount of free alkali metal hydroxide in the aqueous layer from the neutralization step is suicient to yield a neutral eiuent. Therefore, the amount of sludgev mixed with the organic salt layer is sufficient to provide enough acid ions to react with all` of the alkali metal in the organic salt layer in accordance with, the equation and the amount of free alkali metal hydroxide in the aqueous layer from the neutralizing step is suicient to neutralize the mixture of organic salt layer and acid sludge. Thus, there is produced a fuel oil of improved stability with respect to color and sediment and at the same time the problem of` disposing of the organic salt layer and the acid sludge is eliminated.
The free organic acids, i.e., phenols, etc. and the free organic bases from the acid sludge can be recovered or used as a source of fuel, or used as a` component of industrial fuels. The substantially neutral aqueous solution of neutral salts presents no pollution problem and can be discharged to any sewer or water course.
In controlling the neutralization of the organic salt layer with the acid sludge it has been found that about 60 pounds of acid sludge are required per 100 pounds of organic salt. However,` for practical purposes itis sufcient to draw-off the organic salt layer, mix sufficient acid sludge therewith to produce a mixture which is acid to methyl orange and then to add suicient of the` aqueous solution of the neutralizing treat to make `the mixture neutral. Control by means of a titrating electrode to pH 9 in the first step and to pH 7 with the aqueous solution from the neutralizing step also provides satisfactory results.
The accompanying drawing constitutes a labelled owsheet diagrammatically illustrating the method described above.
I claim:
1. In the method of treating fuel fractions of petroleum oil boiling above the gasoline range which are unstable to at least one of color and sediment which consists essentially of contacting a fuel fraction of petroleum oil boiling above the gasoline range with an aqueous alkali metal hydroxide treating solution having a density of at least 40 Baume, and with an oil-to-treating-solution ratio of about 4:1 to 30:1, to obtain a partially treatedv oil and alkali metal salts of organic constituents of said petroleum fraction having replaceable acidic hydrogen atoms; separating partially treated oil from the aforesaid alkali metal organic salts and aqueous alkali metal hydroxide; separating said alkali metal organic salts from 4. aqueous alkaliA metal hydroxide; immediately contacting said partially treated oil with a solution containing at `least weight percent sulfuric acid to obtain twicetreated petroleum fraction and acid sludge; separating twice-treated petroleum fraction from acid sludge; immediately contacting twice-treated petroleum fraction with suicient aqueous alkali metal hydroxide to produce neutralized twice-treated oil; separating neutralized twicetreated oil from aqueous alkali` metal` hydroxide; waterwashing said neutralizedV twice-treated petroleum fraction to, produce water-washed, neutralized, twice-treated petroleum fraction; and separating water-washed, neutralized, twice-treated petroleum fraction from washwater, the improvement that comprises mixing the aforesaid alkali metal salts of organic constituents having replaceable acidic hydrogen atoms, 4said acid sludge and said aqueous alkali metal hydroxide from the neutralization of said twice-treated oil in proportions such that a neutral aqueous layer separates from a layer of organic material including said organic constituents having replaceable acidic hydrogen; flowing said neutral aqueous layer to a public sewer or water course; and disposing of said layer of organic material in a manner such as not to pollute the local water courses.
2. The method of claim 1 wherein the twice treated oil is neutralized with aqueous alkali metal hydroxide containing 10 to 20 weight percent alkali metal hydroxide.
3. The method of claim 1 wherein the partially treated oil is `treated with spent alkylation acid containing at least 90 weight percent sulfuric acid.
4. The method of claim 1 wherein at least a portion of the aqueous alkali metal hydroxide separated from the partially treated petroleum fraction and the organic salts is concentrated to at least the density of the original aqueous alkali metal hydroxide treating solution.
5. The method of treating fuel fractions of petroleum oil boiling above the gasoline range as set forth and described in claim 1 wherein the layer of organic material is mixed with industrial fuel.
6. The method of treating fuel fractions of petroleum oil boiling above the gasoline range as set forth and described in claim 1 wherein at least one of phenolic materials, carboxylic acids, and organic bases` is separated from said layer of organic material.
References Cited in the le of this patent UNlTED STATES PATENTS 1,936,210 Retailliau Nov. 21, 1933 1,938,094 Campbell Dec. 5`, 1933' 1,953,336 Campbell Apr. 3, 1934 2,244,164 Lazar June 3, 1941 2,293,253 Galindo ...7-...,. Aug. 18, 1942
Claims (1)
1. IN THE METHOD OF TREATING FUEL FRACTIONS OF PETROLEUM OIL BOILING ABOVE THE GASOLINE RANGE WHICH ARE UNSTABLE TO AT LEAST ONE OF COLOR AND SEDIMENT WHICH CONSISTS ESSENTIALLY OF CONTACTING A FUEL FRACTION OF PETROLEUM OIL BOILING ABOVE THE GASOLINE RANGE WITH AN AQUEOUS ALKALI METAL HYDROXIDE TREATING SOLUTION HAVING A DENSITY OF AT LEAST 40* BAUME AND WITH AN OIL-TO-TREATING-SOLUTION RATIO OF ABOUT 4:1 TO 30:1, TO OBTAIN A PARTIALLY TREATED OIL AND ALKALI METAL SALTS OF ORGANIC CONSTITUENTS OF SAID PETROLEUM FRACTION HAVING REPLACEMENT ACIDIC HYDROGEN ATOMS, SEPARATING PARTIALLY TREATED OIL FROM THE AFORESAID ALKALI METAL ORGANIC SALTS AND AQUEOUS ALKALI METAL HYDROXIDE, SEPARATING SAID ALKALI METAL ORGANIC SALTS FROM AQUEOUS ALKALI METAL HYDROXIDE, IMMEDIATELY CONTACTING SAID PARTIALLY TREATED OIL WITH A SOLUTION CONTAINING AT LEAST 90 WEIGHT PERCENT SULFURIC ACID TO OBTAIN TWICETREATED PETROLEUM FRACTION AND ACID SLUDGE, SEPARATING TWICE-TREATED PETROLEUM FRACTION FROM ACID SLUDGE, IMMEDIATELY CONTACTING TWICE-TREATED PETROLEUM FRACTION WITH SUFFICIENT AQUEOUS ALKALI METAL HYDROXIDE TO PRODUCE
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US593785A US2959539A (en) | 1956-06-25 | 1956-06-25 | Balanced alkali-acid stabilization of fuel oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US593785A US2959539A (en) | 1956-06-25 | 1956-06-25 | Balanced alkali-acid stabilization of fuel oils |
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| Publication Number | Publication Date |
|---|---|
| US2959539A true US2959539A (en) | 1960-11-08 |
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| US593785A Expired - Lifetime US2959539A (en) | 1956-06-25 | 1956-06-25 | Balanced alkali-acid stabilization of fuel oils |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3048218A (en) * | 1958-09-23 | 1962-08-07 | Rubber & Fibre Chemical Corp | Drum drier for evaporating solvent from a solution of unvulcanized rubber |
| US3186934A (en) * | 1961-09-27 | 1965-06-01 | Universal Oil Prod Co | Recovery of acid oils |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1936210A (en) * | 1929-11-11 | 1933-11-21 | Shell Dev | Process of treating cracked petroleum distillates |
| US1938094A (en) * | 1929-04-24 | 1933-12-05 | Sumner E Campbell | Process for decolorizing hydrocarbon distillates |
| US1953336A (en) * | 1931-05-25 | 1934-04-03 | Summer E Campbell | Process of refining oil |
| US2244164A (en) * | 1938-05-23 | 1941-06-03 | Tide Water Associated Oil Comp | Treatment of light petroleum distillates |
| US2293253A (en) * | 1940-01-08 | 1942-08-18 | Tide Water Associated Oil Comp | Handling of acid sludges |
-
1956
- 1956-06-25 US US593785A patent/US2959539A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1938094A (en) * | 1929-04-24 | 1933-12-05 | Sumner E Campbell | Process for decolorizing hydrocarbon distillates |
| US1936210A (en) * | 1929-11-11 | 1933-11-21 | Shell Dev | Process of treating cracked petroleum distillates |
| US1953336A (en) * | 1931-05-25 | 1934-04-03 | Summer E Campbell | Process of refining oil |
| US2244164A (en) * | 1938-05-23 | 1941-06-03 | Tide Water Associated Oil Comp | Treatment of light petroleum distillates |
| US2293253A (en) * | 1940-01-08 | 1942-08-18 | Tide Water Associated Oil Comp | Handling of acid sludges |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3048218A (en) * | 1958-09-23 | 1962-08-07 | Rubber & Fibre Chemical Corp | Drum drier for evaporating solvent from a solution of unvulcanized rubber |
| US3186934A (en) * | 1961-09-27 | 1965-06-01 | Universal Oil Prod Co | Recovery of acid oils |
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