US1823558A - Purification of tar acid-bearing oils - Google Patents
Purification of tar acid-bearing oils Download PDFInfo
- Publication number
- US1823558A US1823558A US137174A US13717426A US1823558A US 1823558 A US1823558 A US 1823558A US 137174 A US137174 A US 137174A US 13717426 A US13717426 A US 13717426A US 1823558 A US1823558 A US 1823558A
- Authority
- US
- United States
- Prior art keywords
- oil
- tar
- oils
- color
- tar acid
- 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
- 239000003921 oil Substances 0.000 title description 63
- 239000011289 tar acid Substances 0.000 title description 19
- 238000000746 purification Methods 0.000 title description 5
- 239000011269 tar Substances 0.000 description 23
- 238000000034 method Methods 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 20
- 239000002253 acid Substances 0.000 description 18
- 150000007513 acids Chemical class 0.000 description 18
- 239000007864 aqueous solution Substances 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- 238000011282 treatment Methods 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000645 desinfectant Substances 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- 230000001376 precipitating effect Effects 0.000 description 5
- 150000008043 acidic salts Chemical class 0.000 description 4
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 4
- 230000002070 germicidal effect Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000004821 distillation Methods 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PNZVFASWDSMJER-UHFFFAOYSA-N acetic acid;lead Chemical compound [Pb].CC(O)=O PNZVFASWDSMJER-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- MJBPUQUGJNAPAZ-AWEZNQCLSA-N butin Chemical compound C1([C@@H]2CC(=O)C3=CC=C(C=C3O2)O)=CC=C(O)C(O)=C1 MJBPUQUGJNAPAZ-AWEZNQCLSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 229910000286 fullers earth Inorganic materials 0.000 description 2
- 229910001385 heavy metal Inorganic materials 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- MJBPUQUGJNAPAZ-UHFFFAOYSA-N Butine Natural products O1C2=CC(O)=CC=C2C(=O)CC1C1=CC=C(O)C(O)=C1 MJBPUQUGJNAPAZ-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 241001137327 Vireo Species 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 238000010000 carbonizing Methods 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000004058 oil shale Substances 0.000 description 1
- -1 parblack Inorganic materials 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000003079 shale oil Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 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
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/06—Metal salts, or metal salts deposited on a carrier
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10C—WORKING-UP PITCH, ASPHALT, BITUMEN, TAR; PYROLIGNEOUS ACID
- C10C1/00—Working-up tar
- C10C1/20—Refining by chemical means inorganic or organic compounds
Definitions
- the present invention relates to the purification of tar acid-bearing oils, and more particularly to a process for eliminating colorproducing compounds from tar acid-bearing 5 oils containing them.
- Some tar acid-bearing oils (such as low temperature tars, blast furnacetars, vertical retort tars, shale oils and other liquid 'condensates resulting from the distillation of bituminous material under carbonizing conditions mild enoughto preserve the liquid by-products in a substantially primary and undecomposed form) contain certain impurities which render them unsatisfactory or make them undesirable for certain uses.
- the primary object of the present invention is to provide a process for removing color producing compounds of the type referred to from tar acid-bearing oils containing them.
- tar acid-bearing oils of the class described for use in the manufacture of disinfectants, animal dipsand similar products
- the oils have been subjected to washing treatments with aqueous sodium carbonate solution.
- This treatment failsto give even approximately complete removal of the color forming matter except with oils which contain unusually small amounts of such colorproducing bodies.
- washing with dilute caustic soda solution has been employed, but this treatment involves a very considerable loss of the desirable tar acids of-high germicidal.
- Another objectof the present invention is to provide a process by which the color-producing bodies present in such tar acid-bearing oils can be cheaply and completely extracted without also removing valuable tar acids.
- the. process for purifying tar acid-bearing oils forming the subject of the present invention in its preferred form, consists in precipitating the color-producing bodies from the oil by means of a water-solublenon-acidic salt of aheavy metal, parblack, fullers earth, activatedcarbon or the tar acids from a tar acid-bearing oil. No favorable catalysis of secondary reactions with the color-producing compounds appears to takeoplace, and practically none of the desirable and valuable monohydroxy tar acids of high germicidal value are precipitated from theoil.
- disinfectant emulsions can be prepared from a soap base blend of the oil which will not turn pink, and the purification of the oil can be completed at relatively small expense without materially lowering the value of the disinfectants and the germicidal agents prepared therefrom.
- tar acid-bearing oil is used in the description and claims to include all tar acid containing oils or liquid condensates obtained in the distillation of coal or oil shale.
- the tar acid content of most of such oils, and particularly those obtained by the low temperature distillation of coal often consists almost entirely of compounds, which, while they resemble the, phenols or tar acids of coke oven tar in some of their properties, do not come within the generally accepted definition of a phenol, but are rather hydroxyl derivatives of cyclic hydrocarbons which are nonaromatic in character, having hydrogen and alkvl side chains attached to the aromatic nucleus.
- the method of removing color-producing compounds, including ortho-dihydric tar acids, from an oil containing the same together with other tar acids without substantial removal of the latter from the oil which comprises agitating a mixture of the oil and an aqueous solution of a non-acidic salt of a metal which forms insoluble compounds with ortho-dihydric tar acids, and separating the insoluble compounds thus formed from the residual oil.
- the method of removing color-producing compounds from an oil containing monohvdric tar acids while conserving the content of the latter which comprises agitating the oil for about thirtv minutes at a temperature of about C. with about an equal volume of a 10% aqueous solution of normal lead acetate, separating the aqueous layer from the treated oil. mixing with the latter a small percentage of a filter aid material, and filtering to separate the insoluble metal salt precipitates of the color-producing bodies from the oil filtrate.
- the method of removing color-producing compounds from an oil containing monohvdric tar acids while conserving the content of the latter which comprises agitating the oil with an aqueous solution of a non-acidic salt of a heavy metal, separating the aqueous solution of excess treating agent from the treated oil, and employing the solution thus separated in purifying another batch of oils containing tar acid.
- the method of removing color-producing compounds from an oil containing monohvdric tar acids while conserving the content of the latter which comprises agitating the oils with an aqueous solution of a non-acidic salt of a heavy metal, separating the aqueous layer from the treated oil, mixing with the oil layer a small percentage of a filter aid and filtering to separate the insoluble metal salt precipitates from the oil filtrate.
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)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
Description
Patented Sept. 15, 1931 vireo STATES PATENT OFFICE STEPHEN P. BURKE, OF NEW YORK, N. Y., ASSIGNOB TO OOMBUSTION-UTILITIES CORPORATION, OF NEW YORK, N. Y., A CORPORATION'OF MAINE PURIFICATION OF TAR ACID-BEARING OILS No Drawing.
7 The present invention relates to the purification of tar acid-bearing oils, and more particularly to a process for eliminating colorproducing compounds from tar acid-bearing 5 oils containing them. I I
Some tar acid-bearing oils (such as low temperature tars, blast furnacetars, vertical retort tars, shale oils and other liquid 'condensates resulting from the distillation of bituminous material under carbonizing conditions mild enoughto preserve the liquid by-products in a substantially primary and undecomposed form) contain certain impurities which render them unsatisfactory or make them undesirable for certain uses. One form in which these impurities manifest themselves is in the production of colored compounds when such oils are "used for the manufacture of disinfectants, animal dips, saponified cresol or tar acid'solutions and related products; After exhaustive and thorough investigation of the chemical compositions and properties of these colored compounds their origin has been traced to certain strongly reducing ortho-dihydrictar acids, similar to but not including catechol. Thus one of these bodies has been isolated and identified as a new homologue of catechol comprising 3, 4- or 3, G-dimethyl catechol.
The primary object of the present invention is to provide a process for removing color producing compounds of the type referred to from tar acid-bearing oils containing them. Heretofore in preparing and refining tar acid-bearing oils of the class described for use in the manufacture of disinfectants, animal dipsand similar products, the oils have been subjected to washing treatments with aqueous sodium carbonate solution. This treatment, however, failsto give even approximately complete removal of the color forming matter except with oils which contain unusually small amounts of such colorproducing bodies. In treating other tar acid-bearing oils, washing with dilute caustic soda solution has been employed, but this treatment involves a very considerable loss of the desirable tar acids of-high germicidal.
value, which areextracted together with the color-forming materials. by the caustic soda Application filed September 22, 1926. Serial No. 137,174.
treatment. Another method has been recent lyproposed for removing these color producing compounds from coal tar distillates and the like, which comprises washing theoils with aqueous solutions of weakly alkaline buffer agents such as calcium hydroxide and ammonium hydroxide. While this latter method of treatingthe'oils has proved to be much more satisfactory than methods now in use in the trade,- it has been found that the action of the alkaline buffer agents is often incomplete in the case of taracid-bearing oils containing appreciably large quantities of color-producing matter. Fractionation of the oilswith rejection of the portion boiling above-230 C. has alsobeen advocated, but since this excludes the larger'portion of the oil, including most of the high boiling tar acids which are the most valuable germicides present in the oils, the method is not commercially feasible.
Another objectof the present invention is to provide a process by which the color-producing bodies present in such tar acid-bearing oils can be cheaply and completely extracted without also removing valuable tar acids.
With these and other objects and features in view the invention consists in the process for purifying tar acid-containing oils hereinafter described and particularly defined in the claims. a
Essentially the. process for purifying tar acid-bearing oils forming the subject of the present invention, in its preferred form, consists in precipitating the color-producing bodies from the oil by means of a water-solublenon-acidic salt of aheavy metal, parblack, fullers earth, activatedcarbon or the tar acids from a tar acid-bearing oil. No favorable catalysis of secondary reactions with the color-producing compounds appears to takeoplace, and practically none of the desirable and valuable monohydroxy tar acids of high germicidal value are precipitated from theoil.
The following procedure isset forth as an example of a satisfactory method of treating tar acid-bearingoilshaving a relatively bid owing-tothe presence of gelatinous lead salts of color-producing impurities original- 1y present in the oil, was mixed with 1% of its weight of a filter-aid (for example bone like) and filtered with suction. The resulting oil filtrate was clear, and a disinfectant prepared from it by means of. rosin soap gave an emuls1on with water which was practically free of red color. The oil may be distilled either before or after treatment if desired, although such distillation is not necessary for the'removal of the color-producing bodies. Without the use of some filter aid such as bone black, fullers earth or the like, experiments have shown that it is extremely difficult to get a complete, separation of the insoluble lead salts of the color-producing-bodies from the oil in which they are suspended. Filtration or centrifuging of the oil has been tried, butin many cases the oil obtained by either of these treatments is not entirely freed ofv the insoluble salts of the color-producing bodies. It has been found desirable to heat the oil during the period of agitation with thetreating agent, forthe reason that since the reaction leading to'the formation of insoluble metal salts takes place in the aqueous phase,the heat increases the solubility of thecolor-forming material in the aqueous phaseand thereby hastens the completion of the reaction and insures the completeness of interaction between the reagent and the color-producing impurities. Once formed, the insoluble metal salts leave the aqueous phase and pass into the oil, where'they remain in suspension. If an excess of the precipitating agent is present in the aqueous solution, the latter may be drawn off and used again for treating another batch of oil, and this process reagent remains in the aqueous solution.
It is not intended by the above description to limit the scope of the present invention to the treatment of oils containing definite compounds, nor to the use of definite proportions of the precipitating agent, nor to the employment of particular temperatures or particular time limitations of agitation, nor to the use of any particular metal salt as a precipitating agent or particular methods of separating the oil and insoluble material@ Any metal salt which gives an insoluble compound on interaction with orthodihydric tar acids of the class referred to may be employed. The process is applicable not only to the treatment of the tars themselves, but also to the treatment of a tar acid fraction alone (unadmixed with hydrocarbon oil), The volume 'of the precipitating agent used is preferably limited to a. slight excess above that required for removing the color-producing impurities.
By employing the process forming the subject matter of the present invention for the purification of tar acid-bearing oil, disinfectant emulsions can be prepared from a soap base blend of the oil which will not turn pink, and the purification of the oil can be completed at relatively small expense without materially lowering the value of the disinfectants and the germicidal agents prepared therefrom.
' The term tar acid-bearing oil is used in the description and claims to include all tar acid containing oils or liquid condensates obtained in the distillation of coal or oil shale. The tar acid content of most of such oils, and particularly those obtained by the low temperature distillation of coal, often consists almost entirely of compounds, which, while they resemble the, phenols or tar acids of coke oven tar in some of their properties, do not come within the generally accepted definition of a phenol, but are rather hydroxyl derivatives of cyclic hydrocarbons which are nonaromatic in character, having hydrogen and alkvl side chains attached to the aromatic nucleus.
The preferred form of the invention having been thus described, what is claimed as new 1s: I
1; The method of removing color-produc- Iing compounds from an oil containing mono- 7 producing bodies thereby precipitated from peatedas long as suiiicientprecipitating the residual purified oil. 3. The method of removing color-producmg compounds, including ortho-dihydric tar acids, from an oil containing the same together with other tar acids without substantial removal of the latter from the oil which comprises agitating a mixture of the oil and a non-acidic salt ofa metal which forms insoluble compounds with ortho-dihydric tar acids, and subsequently separating the purified oil and the, insoluble compounds thus formed.
4. The method of removing color-producing compounds, including ortho-dihydric tar acids, from an oil containing the same together with other tar acids without substantial removal of the latter from the oil which comprises agitating a mixture of the oil and an aqueous solution of a non-acidic salt of a metal which forms insoluble compounds with ortho-dihydric tar acids, and separating the insoluble compounds thus formed from the residual oil.
5. The method of removing color-producing compounds from an oil containing monohvdric tar acids while conserving the content of the latter, which comprises agitating the oil for about thirtv minutes at a temperature of about C. with about an equal volume of a 10% aqueous solution of normal lead acetate, separating the aqueous layer from the treated oil. mixing with the latter a small percentage of a filter aid material, and filtering to separate the insoluble metal salt precipitates of the color-producing bodies from the oil filtrate.
6. The method of removing color-producing compounds from an oil containing monohvdric tar acids while conserving the content of the latter, which comprises agitating the oils with an aqueous solution of normal lead acetate.
7. The method of removing color-producing compounds from an oil containing monohvdric tar acids while conserving the content of the latter, which comprises agitating the oil with an aqueous solution of a non-acidic salt of a heavy metal, separating the aqueous solution of excess treating agent from the treated oil, and employing the solution thus separated in purifying another batch of oils containing tar acid.
8. The method of removing color-producing compounds from an oil containing monohvdric tar acids while conserving the content of the latter, which comprises agitating the oils with an aqueous solution of a non-acidic salt of a heavy metal, separating the aqueous layer from the treated oil, mixing with the oil layer a small percentage of a filter aid and filtering to separate the insoluble metal salt precipitates from the oil filtrate.
In testimony whereof I aflix mv signature.
STEPHEN P. BURKE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US137174A US1823558A (en) | 1926-09-22 | 1926-09-22 | Purification of tar acid-bearing oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US137174A US1823558A (en) | 1926-09-22 | 1926-09-22 | Purification of tar acid-bearing oils |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1823558A true US1823558A (en) | 1931-09-15 |
Family
ID=22476133
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US137174A Expired - Lifetime US1823558A (en) | 1926-09-22 | 1926-09-22 | Purification of tar acid-bearing oils |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1823558A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2493596A (en) * | 1946-06-20 | 1950-01-03 | Shell Dev | Process for refining hydrocarbon oils |
| US2588346A (en) * | 1949-10-22 | 1952-03-11 | Houdry Process Corp | Refining gasoline and petroleum oils with aqueous antimony trichloride |
| US2626891A (en) * | 1950-10-06 | 1953-01-27 | Standard Oil Dev Co | Gasoline treating process |
-
1926
- 1926-09-22 US US137174A patent/US1823558A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2493596A (en) * | 1946-06-20 | 1950-01-03 | Shell Dev | Process for refining hydrocarbon oils |
| US2588346A (en) * | 1949-10-22 | 1952-03-11 | Houdry Process Corp | Refining gasoline and petroleum oils with aqueous antimony trichloride |
| US2626891A (en) * | 1950-10-06 | 1953-01-27 | Standard Oil Dev Co | Gasoline treating process |
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