US2034197A - Treatment of hydrocarbon oils - Google Patents
Treatment of hydrocarbon oils Download PDFInfo
- Publication number
- US2034197A US2034197A US582155A US58215531A US2034197A US 2034197 A US2034197 A US 2034197A US 582155 A US582155 A US 582155A US 58215531 A US58215531 A US 58215531A US 2034197 A US2034197 A US 2034197A
- Authority
- US
- United States
- Prior art keywords
- vapors
- treatment
- treating
- gasoline
- solutions
- 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
Links
- 238000011282 treatment Methods 0.000 title description 25
- 229930195733 hydrocarbon Natural products 0.000 title description 12
- 150000002430 hydrocarbons Chemical class 0.000 title description 12
- 239000004215 Carbon black (E152) Substances 0.000 title description 11
- 239000003921 oil Substances 0.000 title description 7
- 239000000243 solution Substances 0.000 description 20
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 8
- 239000005864 Sulphur Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 230000008569 process Effects 0.000 description 8
- 238000009835 boiling Methods 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 238000005336 cracking Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000009471 action Effects 0.000 description 4
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 4
- 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 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000001117 sulphuric acid Substances 0.000 description 3
- 235000011149 sulphuric acid Nutrition 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000012286 potassium permanganate Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- -1 their chromates Chemical class 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000274 adsorptive effect Effects 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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
- C10G19/00—Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment
-
- 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
- C10G27/00—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation
- C10G27/04—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen
- C10G27/06—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen in the presence of alkaline solutions
-
- 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
- C10G27/00—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation
- C10G27/04—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen
- C10G27/12—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen with oxygen-generating compounds, e.g. per-compounds, chromic acid, chromates
Definitions
- This invention relates to the treatment of hydrocarbon oils and refers more particularly to the treatment of low boiling cracked distillates though similar distillates produced by the straight run or non-cracking distillation of crude petroleums may also be treated.
- the invention contemplates treatment of low boiling hydrocarbon vapors by means adapted to controllably reduce their content of undesirable constituents such as the morehighly unsaturated hydrocarbons which increase the gum-forming tendencies of the condensed distillate and some of the sulphur containing hydrocarbon derivatives which have a corrosive action upon metals either before or after their combustion when the distillates which contain them are burned in internal combustion engine cylinders.
- undesirable constituents such as the morehighly unsaturated hydrocarbons which increase the gum-forming tendencies of the condensed distillate and some of the sulphur containing hydrocarbon derivatives which have a corrosive action upon metals either before or after their combustion when the distillates which contain them are burned in internal combustion engine cylinders.
- the more generally used combination of steps employed to produce marketable gasoline by cracking the heavier and less desirable portions of crude petroleums consists in producing first a raw pressure distillate containing a high percentage of gasoline boiling point range fractions, treating this distillate with various chemical re agents such as caustic soda solutions, sulphuric acid of varying strength, sodium plumbite, etc., to reduce unsaturation and sulphur and then rerunning the treated distillate to produce a finished gasoline free from heavy polymerized and condensed reaction products which remain behind in the distillation.
- various chemical re agents such as caustic soda solutions, sulphuric acid of varying strength, sodium plumbite, etc.
- the invention comprises treating hydrocarbon oil vapors, particularly cracked hydrocarbon oil vapors, with solutions of alkali hydroxides containing salts of oxidizing acids.
- solutions of the commoner alkali hydroxides such as those of sodium and potassium and also to employ the more readily available oxidizing salts of sodium and potassium such as their chromates, 5 dichromates, perchromates, manganates, permanganates, nitrates, etc.
- oxidizing salts of sodium and potassium such as their chromates, 5 dichromates, perchromates, manganates, permanganates, nitrates, etc.
- the use of the alkalis and salts mentioned in various combinations adapted to particular treatments will only be limited by their respective solubilities. However, it is preferred to use approximately saturated solutions since under the temperature and pressure conditions under which vapors are generally treated Weaker solutions are rapidly concentrated on account of the evaporation of the solvent.
- the treating solution may be brought into contact with the vapors in a variety of ways, the simplest being to introduce the solution at the top of a bafiied treating tower countercurrent to an ascending stream of vapors, the spent solution and reaction products being withdrawn from the bottom of the tower and the treated vapors further fractionated to produce distillates of the boiling point range desired in the finished gasoline.
- the conditions of treatment are such that there is a separation of liquid hydrocarbon refiuxes in the tower, these may be separately removed from the tower at a level above the level of the spent aqueous solution or the total liquid products may be withdrawn together and separated outside the tower.
- Treatments may also be conducted by introducing the treating solutions into 'the cracked vapors which are passing downwardly over solid contact reagents such as those of the non-metallic or siliceous type or masses whose action is due 40 essentially to their metallic content.
- solid contact reagents such as those of the non-metallic or siliceous type or masses whose action is due 40 essentially to their metallic content.
- Fuller's earth is an example of the siliceous adsorbent material and crushed rock or porcelain exemplifies any material which may be so used which has no distinctly adsorptive properties but merely acts as a distributing agent. Solutions may be injected into the vapors in such downfiow treatments through atomizing devices such as sprays or nozzles to insure good contact therewith; the choice of downfiow, concurrent treatment being determined to some extent by the amount of condensation which ensues and other factors.
- Suitable treatment may also be effected by bubbling the vapors to be treated through stationary pools of solution, the vapors then passing to fractionating equipment for the production of the final end-product gasoline.
- treatment may be at times sufficient in itself in producing desired treating efifects or it may be employed in conjunction with other treatments.
- it may be applied before or after the use of sulphuric acid in case it is feasible to conduct sulphuric acid treatments by the use of dilute solutions of or solutions containing salts as spacing agents.
- Other treating steps that may be employed in conjunction with the process of the invention may be the use of adsorbent materials to remove polymers, metals or metal oxides to remove sulphur and the use of relatively inert filtering materials to remove entrained particles from the vapors.
- steam may be introduced to lower the rate of evaporation of the solvent, and prevent separation of solids and the possibility of plugging up treating apparatus.
- the effects produced upon hydrocarbon oil vapors by the use of alkali solutions containing oxidizing salts is to produce a polymerizing action upon the gum or resin-forming constituents of the vapors which removes substantially all of the highly unsaturated di and triolefins and also produces a limited desulphurizing effect, the extent of the latter action being determined by the type of sulphur compounds present in the vapors, the composition of the treating solution and the operating conditions.
- the solutions used according to the process of the invention have a sweetening and desulphurizing action which is of value in the treatment of hydrocarbons generally as well as in special cases, such as in the treatment of the lower boiling vapors from stabilizing plants containing large percentages of propane, butane and isobutane.
- vapors of approximate gasoline boiling point range arising from the final fractionator of a cracking plant operating upon a mixture of Mid- Continent residuum and heavy gas oil may be passed upwardly through a treating tower couri tercurrent to a descending solution of potassium permanganate and caustic soda, the solution being substantially saturated with the alkali at the temperature of operation and containing approximately 5% by weight of potassium permanganate.
- a sufficient amount of steam may be introduced with the cracked vapors to inhibit the evaporation of water from the solution and prevent separation of solid salts.
- the amount of treating solution need not be large if proper recycling is practiced and may not exceed one to five percent by volume of gasoline condensed.
- the following tabulation shows a comparison of the properties of the gasoline which would be produced from the plant if no treatment were given the vapors and the gasoline produced by the treatment of the vapors in the manner just described.
- the loss in yield of gasoline may be less than 1% as a result of A greater percentage reduction in sulphur may be noted with hydrocarbon mixtures containing higher sulphur contents such as cracked distillates or vapors from California, Venezuela and Mexican charging stocks. 1
- a process for refining hydrocarbon vapors which comprises treating the vapors with a concentrated aqueous solution of an alkali metal hydroxide containing an alkali metal permanganate.
- a process for refining hydrocarbon vapors which comprises treating the vapors with an aqueous solution substantially saturated with an alkali metal hydroxide and containing a relatively small amount of a permanganate of an alkali metal. 7
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 Mar. 17, 1936 UNITED STATES PATENT OFFICE TREATMENT OF HYDROGARBON OILS ware No Drawing. Application December 19, 1931,
' Serial No. 582,155
2 Claims.
This invention relates to the treatment of hydrocarbon oils and refers more particularly to the treatment of low boiling cracked distillates though similar distillates produced by the straight run or non-cracking distillation of crude petroleums may also be treated.
More specifically the invention contemplates treatment of low boiling hydrocarbon vapors by means adapted to controllably reduce their content of undesirable constituents such as the morehighly unsaturated hydrocarbons which increase the gum-forming tendencies of the condensed distillate and some of the sulphur containing hydrocarbon derivatives which have a corrosive action upon metals either before or after their combustion when the distillates which contain them are burned in internal combustion engine cylinders.
The more generally used combination of steps employed to produce marketable gasoline by cracking the heavier and less desirable portions of crude petroleums consists in producing first a raw pressure distillate containing a high percentage of gasoline boiling point range fractions, treating this distillate with various chemical re agents such as caustic soda solutions, sulphuric acid of varying strength, sodium plumbite, etc., to reduce unsaturation and sulphur and then rerunning the treated distillate to produce a finished gasoline free from heavy polymerized and condensed reaction products which remain behind in the distillation. Obviously if the necessary chemical treatment could be done upon the vapors prior to their fractionation the treatment could be made continuous along with the operation of the cracking plant, the rerunning step eliminated and a considerable quantity of heat conserved which would add to the overall efiiciency of the operation. Such treatments, however, have met with only partial success commercially owing to the fact that treatments must be conducted at the temperature of the vapors which is usually high enough to cause an undue increase in the reactivity of the vapors with the treating reagents employed. The present invention provides an improvement in vapor phase treating processes which if not always adequate in itself for a complete treatment, furnishes a step which is of great value in connection with other vapor phase chemical treatments.
In one specific embodiment the invention comprises treating hydrocarbon oil vapors, particularly cracked hydrocarbon oil vapors, with solutions of alkali hydroxides containing salts of oxidizing acids.
For economic reasons it is preferred to employ solutions of the commoner alkali hydroxides such as those of sodium and potassium and also to employ the more readily available oxidizing salts of sodium and potassium such as their chromates, 5 dichromates, perchromates, manganates, permanganates, nitrates, etc. The use of the alkalis and salts mentioned in various combinations adapted to particular treatments will only be limited by their respective solubilities. However, it is preferred to use approximately saturated solutions since under the temperature and pressure conditions under which vapors are generally treated Weaker solutions are rapidly concentrated on account of the evaporation of the solvent.
In conducting treatments within the scope of the invention upon Vapors of approximate gasoline boiling point range arising from cracking operations the treating solution may be brought into contact with the vapors in a variety of ways, the simplest being to introduce the solution at the top of a bafiied treating tower countercurrent to an ascending stream of vapors, the spent solution and reaction products being withdrawn from the bottom of the tower and the treated vapors further fractionated to produce distillates of the boiling point range desired in the finished gasoline. When the conditions of treatment are such that there is a separation of liquid hydrocarbon refiuxes in the tower, these may be separately removed from the tower at a level above the level of the spent aqueous solution or the total liquid products may be withdrawn together and separated outside the tower.
Treatments may also be conducted by introducing the treating solutions into 'the cracked vapors which are passing downwardly over solid contact reagents such as those of the non-metallic or siliceous type or masses whose action is due 40 essentially to their metallic content. Fuller's earth is an example of the siliceous adsorbent material and crushed rock or porcelain exemplifies any material which may be so used which has no distinctly adsorptive properties but merely acts as a distributing agent. Solutions may be injected into the vapors in such downfiow treatments through atomizing devices such as sprays or nozzles to insure good contact therewith; the choice of downfiow, concurrent treatment being determined to some extent by the amount of condensation which ensues and other factors.
Suitable treatment may also be effected by bubbling the vapors to be treated through stationary pools of solution, the vapors then passing to fractionating equipment for the production of the final end-product gasoline.
As already stated in the preceding paragraph, treatment may be at times sufficient in itself in producing desired treating efifects or it may be employed in conjunction with other treatments. For example, it may be applied before or after the use of sulphuric acid in case it is feasible to conduct sulphuric acid treatments by the use of dilute solutions of or solutions containing salts as spacing agents. Other treating steps that may be employed in conjunction with the process of the invention may be the use of adsorbent materials to remove polymers, metals or metal oxides to remove sulphur and the use of relatively inert filtering materials to remove entrained particles from the vapors.
To maintain the concentration of the solution at the optimum point steam may be introduced to lower the rate of evaporation of the solvent, and prevent separation of solids and the possibility of plugging up treating apparatus.
In general the effects produced upon hydrocarbon oil vapors by the use of alkali solutions containing oxidizing salts is to produce a polymerizing action upon the gum or resin-forming constituents of the vapors which removes substantially all of the highly unsaturated di and triolefins and also produces a limited desulphurizing effect, the extent of the latter action being determined by the type of sulphur compounds present in the vapors, the composition of the treating solution and the operating conditions. When the vapors contain relatively large amounts of hydrogen sulfide and mercaptans a large amount of desulphurizing may be efiected, while if the sulphur content is due principally to sulphur ethers or thiophene compounds, lesser though very substantial effects upon the reduction of the sulphur content of the vapors may be noted. It may therefore be stated that the solutions used according to the process of the invention have a sweetening and desulphurizing action which is of value in the treatment of hydrocarbons generally as well as in special cases, such as in the treatment of the lower boiling vapors from stabilizing plants containing large percentages of propane, butane and isobutane.
As an example of results obtained by a treatment characteristic of the process of the invention vapors of approximate gasoline boiling point range arising from the final fractionator of a cracking plant operating upon a mixture of Mid- Continent residuum and heavy gas oil may be passed upwardly through a treating tower couri tercurrent to a descending solution of potassium permanganate and caustic soda, the solution being substantially saturated with the alkali at the temperature of operation and containing approximately 5% by weight of potassium permanganate. A sufficient amount of steam may be introduced with the cracked vapors to inhibit the evaporation of water from the solution and prevent separation of solid salts. The amount of treating solution need not be large if proper recycling is practiced and may not exceed one to five percent by volume of gasoline condensed. The following tabulation shows a comparison of the properties of the gasoline which would be produced from the plant if no treatment were given the vapors and the gasoline produced by the treatment of the vapors in the manner just described. The loss in yield of gasoline may be less than 1% as a result of A greater percentage reduction in sulphur may be noted with hydrocarbon mixtures containing higher sulphur contents such as cracked distillates or vapors from California, Venezuela and Mexican charging stocks. 1
The results just cited as typical of those obtainable by the use of the process upon cracked vapors will serve to indicate the value of the process but these results as well as theother descriptive material are only illustrative and the scope of the invention is not to be considered as limited thereto.
I claim as my invention:
1. A process for refining hydrocarbon vapors which comprises treating the vapors with a concentrated aqueous solution of an alkali metal hydroxide containing an alkali metal permanganate.
2. A process for refining hydrocarbon vapors which comprises treating the vapors with an aqueous solution substantially saturated with an alkali metal hydroxide and containing a relatively small amount of a permanganate of an alkali metal. 7
JACQUE C. MORRELL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US582155A US2034197A (en) | 1931-12-19 | 1931-12-19 | Treatment of hydrocarbon oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US582155A US2034197A (en) | 1931-12-19 | 1931-12-19 | Treatment of hydrocarbon oils |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2034197A true US2034197A (en) | 1936-03-17 |
Family
ID=24328061
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US582155A Expired - Lifetime US2034197A (en) | 1931-12-19 | 1931-12-19 | Treatment of hydrocarbon oils |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2034197A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3152070A (en) * | 1961-04-27 | 1964-10-06 | Shell Oil Co | Removal of odor by hydrogenation and oxidation |
| US4049543A (en) * | 1974-03-19 | 1977-09-20 | Ab Nynas-Petroleum | Method for the separation of a mixture of petroleum acids from petroleum distillates containing such a mixture |
-
1931
- 1931-12-19 US US582155A patent/US2034197A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3152070A (en) * | 1961-04-27 | 1964-10-06 | Shell Oil Co | Removal of odor by hydrogenation and oxidation |
| US4049543A (en) * | 1974-03-19 | 1977-09-20 | Ab Nynas-Petroleum | Method for the separation of a mixture of petroleum acids from petroleum distillates containing such a mixture |
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