US1771350A - Process of refining hydrocarbon oils - Google Patents
Process of refining hydrocarbon oils Download PDFInfo
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- US1771350A US1771350A US670780A US67078023A US1771350A US 1771350 A US1771350 A US 1771350A US 670780 A US670780 A US 670780A US 67078023 A US67078023 A US 67078023A US 1771350 A US1771350 A US 1771350A
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- Prior art keywords
- oil
- sulfur
- hydrocarbons
- removal
- hydrocarbon
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- Expired - Lifetime
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- 239000003921 oil Substances 0.000 title description 81
- 229930195733 hydrocarbon Natural products 0.000 title description 51
- 150000002430 hydrocarbons Chemical class 0.000 title description 39
- 238000000034 method Methods 0.000 title description 30
- 239000004215 Carbon black (E152) Substances 0.000 title description 25
- 238000007670 refining Methods 0.000 title description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 24
- 239000011593 sulfur Substances 0.000 description 24
- 229910052717 sulfur Inorganic materials 0.000 description 24
- 239000000243 solution Substances 0.000 description 23
- 230000001476 alcoholic effect Effects 0.000 description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 239000002244 precipitate Substances 0.000 description 14
- -1 shale Substances 0.000 description 14
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 13
- 230000001376 precipitating effect Effects 0.000 description 13
- 238000002156 mixing Methods 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 11
- 229940100892 mercury compound Drugs 0.000 description 11
- 150000002731 mercury compounds Chemical class 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000012535 impurity Substances 0.000 description 7
- 239000012260 resinous material Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 235000011121 sodium hydroxide Nutrition 0.000 description 6
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 150000002611 lead compounds Chemical class 0.000 description 5
- 238000001556 precipitation Methods 0.000 description 5
- 239000012429 reaction media Substances 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- 239000005749 Copper compound Substances 0.000 description 4
- 150000001880 copper compounds Chemical class 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 241001376994 Asolene Species 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
- 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 1
- 238000013019 agitation Methods 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009388 chemical precipitation Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 239000011928 denatured alcohol Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 229940046892 lead acetate Drugs 0.000 description 1
- RLJMLMKIBZAXJO-UHFFFAOYSA-N lead nitrate Chemical compound [O-][N+](=O)O[Pb]O[N+]([O-])=O RLJMLMKIBZAXJO-UHFFFAOYSA-N 0.000 description 1
- 239000003077 lignite Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000013547 stew Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 238000004448 titration Methods 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
- 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
- C10G19/02—Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment with aqueous alkaline solutions
- C10G19/06—Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment with aqueous alkaline solutions with plumbites or plumbates
Definitions
- This invention relates to a process for the separation from hydrocarbon oils of a component or components thereof.
- the rocess may serve to separate from a hydrocar on oil or mixture a valuable component thereof which. is desired in a pure state or it may serve to separate from the oil a deleterious ingredient or impurity or it may serve for the separation of both types of components or components which are objectionable in the oil but valuable when separated from it.
- e process of my invention is based upon the chemical precipitation of the ingredient of the oil to be removed therefrom and conslsts generally in treating the oil with the precipitating agent for the ingredient in the presence of a mutual solvent or reaction medium. 4
- hydrocar on oils and under this expression I mean to include hydrocarbon liquids such as crude petroleum and products obtained therefrom such as distillates and products resulting from cracking operations, products of the destructive distillation of coal, shale, lignite and the like such as crude benzol, natural gas, gasolene, etc.
- the hydrocarbon oil to be treated is a asolene or motor spirit such as may be obtalned by the cracking of a crude petroleum oil and that it contains sulfur, un saturated compounds of the olefine series, acetylene hydrocarbons and diolefines.
- Such an oil has at least three objectionable feathose prepared from petrolepletely removed fining or purification of hydrocarbon oils by the removal therefrom of sulfur if present, acetylene hydrocarbons if resent in objectionable quantity, and diole ne hydrocarbons and resinous or resin-forming bodies which tend to produce the gumming action re ferred to without injury to the remaining components of the oil, and particularly the olefine hydrocarbons.
- the impurities may be quickly and easily and com-
- the invention consists generally in treating an oil with a precipitant for an impurity or component to be separated in the presence of a mutual solvent or reaction medium.
- a precipitant for an impurity or component to be separated in the presence of a mutual solvent or reaction medium.
- the invention may e numerous applications without injury to the puride ending upon the'impurity or component to e separated, the nature of the oil under treatment and the selection of precipitating agent and solvent.
- a suitable solvent capable .of use with a variety of precipitants is alcohol, either ethyl or methyl alcohol or mixtures thereof or denatured alcohol such as a mixture of ethyl alcohol and acetone.
- T he invention is amply illustrated by the following description of the treatment of a hydrocarbon oil of the motor fuel type referred to.
- the oil is mixed in any suitable manner, for instance, by agitation, with an alcoholic solution of a soluble lead compound, for instance basic lead acetate, lead nitrate, or sodium plumbite, preferably the latter, in quantity chemically equivalent to the sulfur content of the oil.
- a soluble lead compound for instance basic lead acetate, lead nitrate, or sodium plumbite, preferably the latter, in quantity chemically equivalent to the sulfur content of the oil.
- the mixing may be carried out at atmospheric or other suitabletemperature.
- the reaction between the lead and the sulfur content of the oil takes place quickly and completely with the formation of a precipimm which is removed in any suitable way as by filtration or sedimentation and decantation.
- the treatment described has been found to remove the sulfur content of the oil very completely so that not even a trace can be detected by ordinary methods.
- the foregoing step for the removal of the last traces of sulfur from the oil may advantageously be preceded by a treatment of the oil for the removal of the bulk of its sulfur content, for instance, by agitating the 011 with a water solution of a ad compound. If the oil contains a relatively large amount of sulfur a portion of which is removable by the old process a considerable saving in the use of the alcoholic solution for the removal of the last traces of sulfur results.
- the oil from which sulfur has been removed may be treated next for the removal of acetylene hydrocarbons.
- This treatment consists simply in mixing the oil at ordinary atmospheric temperature with an alcoholic solution of a copper compound in quantity just equivalent to the precipitatable acetylene hydrocarbon content thereof and separating the resulting precipitate.
- a su1t able copper containing solution for use in this step may be prepared by suspending a copper salt, such as the-chlorid, nitrate, or acetate, in alcohol and saturating the mixture with ammonia.
- the next step of the complete process for the purification of the oil under consideration is the treatment for the removal of diolefines.
- This step consists in mixing the oil at ordinary or other suitable temperature with an alcoholic solution of a mercury compound for instance mercuric chlorid, nitrate, or acetate, in quantity only suflicient to precipitate the diolefine hydrocarbon content of the oil.
- a mercury compound for instance mercuric chlorid, nitrate, or acetate
- the resulting precipitate which contains the mercury and the diolefines is curdy and preferably is separated from the oil by decantation.
- the next step in the process is for the removal of resinous materials. This is accomplished by treating the oil with an alcoholic solution of caustic soda, for instance by agitating the oil with an alcoholic caustic soda solution at atmospheric temperature, and then adding a relatively small amount of water, agitating, and decanting or otherwise separating the clarified oil.
- the clarified oil may then be washed with water to remove dissolved alcohol therefrom and the alcohol recovered by fractionation of the wash Water and the purified oil is finally steam dis tilled.
- the several precipitates formed may if desired be treated by methods known or obvious to a chemist for the recovery therefrom of the precipitating agents and the precipitated materials.
- the diolefine hydrocarbon removing step if an excess of the mercury precipitating agent is used some of the olefine hydrocarbons in the oil may be destroyed by oxidation or converted into undesirable resinous bodies which, as is stated above, are objectionable, due to their umming action, and must be removed, this 0 jectionable feature being in addition to the loss of valuable olefine hydrocarbons.
- This use of the precipitating agents in quantity only sufficient to accomplish the desired precipitation without contamination of the oil is made possible by the use in accordance with my invention of a mutual solvent or re action medium for the oil and the precipi-' tant because in the presence of such a reaction medium the reaction between the precipitat-.
- ing agent and the component of the oil to be precipitated proceeds to'completion quickly without the use of an excess of reagent,
- the quantities of the reagents necessary in each step are readily determined by'a laboratory titration on a sample of the oil under treatment to the precipitation end point in the known manner.
- the invention is not limited to the removal from a hydrocarbon oil of the particular components heretofore referred to excepting as may be required by *the appended claims.
- the process of my invention may be applied for the removal of any single or any particular group of components, for instance, for the removal of sulfur or acetylene hydrocarbons or diolefines, or resinous matter, or any combination thereof or any other impurity or material in any hydrocarbon oil for the precipitation of which a suitable reagent and reaction medium may be found.
- Process of purifying a hydrocarbon oil containing sulfur, diolefine hydrocarbons, acetylene hydrocarbons, olefine hydrocarbons and resinous material which comprises removing the bulk of the sulfur by treating the oil with an aqueous solution of a lead compound, removing the last traces of sulfur from the oil by mixing it with an alcoholic solution of a lead compound and separating the resulting precipitate, removing acetylene hydrocarbons from the oil by mixing it with.
- Process of purifying hydrocarbon oils which comprises precipitating sulfur therefrom by treatment thereof with a leadcom pound in the presence of a solvent for said lead compound which is soluble in the oil, precipitating diolefine hydrocarbons by treatment with a mercury compound in quantity not substantially in excess of the quantity necessary to precipitate said diolefines in the presence of a solvent for said mercury compound which is soluble in the oil, and thereafter removing resinous material from the oil by treatment with an alcoholic caustic soda solution and washing with water.
- Process of purifying a hydrocarbon oil containin sulfur, diolefine hydrocarbons, acetylene Iiydrocarbons, olefine hydrocarbons and resinous material which comprises treating the oil for the removal of sulfur compounds therefrom and thereafter removing acetylene hydrocarbons from the oil by mixing it with an alcoholic solution of a copper compound and separating the resulting precipitate, removing diolefine hydrocarbons from the oil by mixing it with an alcoholic solution of a mercury compound and separating the resulting precipitate, and removing resinous material from the oil by treatment with an alcoholic solution of caustic soda and then washing with water.
- Process of purifying hydrocarbon oils which comprises treating the oil for the removal of the sulfur content thereof and thereafter precipitating diolefine hydrocarbons by treatment with a mercury compound in quantity not substantially in excess of the quantity necessary to precipitate said diolefines in the presence of a solvent for said mercury compound which is soluble in the oil, and thereafter removing resinous material from the oil by treatment'with an alcoholic caustic soda solution and washin with water.
- Process of purifying a hydrocarbon oil containing diolefine and acetylene hydrocarbons which comprises removing the acetylene hydrocarbons from the oil by mixing it with an alcoholic solution of a copper compound and separatin the resulting precipitate, and removing the iolefine hydrocarbons from the oil by mixing it with an alcoholic solution of a mercury compound and separating the resulting precipitate.
- step 6 which comprises removin an impurity of the group consisting of su fur, diolefine hydrocarbons and acetylene hydrocarbons by mixing the oil with an'alcoholic solution of a mercury compound andseparating the resulting precipitate.
- step 7 which comprises removing diolefine hydrocarbons by mixing the oil with an alcoholic solution of a mercury compound and separating the resulting precipitate.
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 July 22, 1930 UNITED STATES PATENT OFFICE ALEXANDER S. RAHAGE, OF DETROIT, 'MICHIGAN, .ASSIGNOB, BY MESNE ASSIGNMENTS, TO GYRO PROCESS CORPORATION, A. CORPORATION OF MICHIGAN PROCESS OF REFINING HYDROCARBON OILS No Drawing. Application filed October 25, 1923, Serial No. 670,780. Renewed October 12, 1928.
This invention relates to a process for the separation from hydrocarbon oils of a component or components thereof. The rocess may serve to separate from a hydrocar on oil or mixture a valuable component thereof which. is desired in a pure state or it may serve to separate from the oil a deleterious ingredient or impurity or it may serve for the separation of both types of components or components which are objectionable in the oil but valuable when separated from it.
The commercial application of the process contemplated at present is thepiirification of hydrocarbon mixtures of the motor fuel type and particularly um oils by crac ring distillation processes and containing objectionable impurities such as sulfur and diolefines, and the invention will be illustrated hereinafter with reference to this application of the process, it being understood however that the invention is not limited to the treatment of any particular hydrocarbon oil or to the purification thereof or to the removal of an particular ingredient or ingredients thereo excepting as may be rerp ifired in the appended claims.
e process of my invention is based upon the chemical precipitation of the ingredient of the oil to be removed therefrom and conslsts generally in treating the oil with the precipitating agent for the ingredient in the presence of a mutual solvent or reaction medium. 4
As stated, the process is applicable generally to hydrocar on oils and under this expression I mean to include hydrocarbon liquids such as crude petroleum and products obtained therefrom such as distillates and products resulting from cracking operations, products of the destructive distillation of coal, shale, lignite and the like such as crude benzol, natural gas, gasolene, etc.
For the purpose of illustration let it be assumed that the hydrocarbon oil to be treated is a asolene or motor spirit such as may be obtalned by the cracking of a crude petroleum oil and that it contains sulfur, un saturated compounds of the olefine series, acetylene hydrocarbons and diolefines. Such an oil has at least three objectionable feathose prepared from petrolepletely removed fining or purification of hydrocarbon oils by the removal therefrom of sulfur if present, acetylene hydrocarbons if resent in objectionable quantity, and diole ne hydrocarbons and resinous or resin-forming bodies which tend to produce the gumming action re ferred to without injury to the remaining components of the oil, and particularly the olefine hydrocarbons.
In processes heretofore employed for the removal of sulfur from hydrocarbon oils, for instance the well known process of Washing the oil with a water solution of a lead'compound, the complete removal of sulfur apparently has been impossible or impracticable, and a substantial and objectionable residue of sulfur is found in oils so refined. Processes have also been devised for the removal of diolefines, for instance, by treatment with sulfuric acid, but this process is objectionable for a number of reasons, among which may be mentioned the incident removal from the oil of valuable olefine hydrocarbons.
By the process of my invention the impurities may be quickly and easily and com- As stated above, the invention consists generally in treating an oil with a precipitant for an impurity or component to be separated in the presence of a mutual solvent or reaction medium. Obviously the invention may e numerous applications without injury to the puride ending upon the'impurity or component to e separated, the nature of the oil under treatment and the selection of precipitating agent and solvent. A suitable solvent capable .of use with a variety of precipitants is alcohol, either ethyl or methyl alcohol or mixtures thereof or denatured alcohol such as a mixture of ethyl alcohol and acetone.
T he invention is amply illustrated by the following description of the treatment of a hydrocarbon oil of the motor fuel type referred to.
For the removal of sulfur the oil is mixed in any suitable manner, for instance, by agitation, with an alcoholic solution of a soluble lead compound, for instance basic lead acetate, lead nitrate, or sodium plumbite, preferably the latter, in quantity chemically equivalent to the sulfur content of the oil.
, The mixing may be carried out at atmospheric or other suitabletemperature. The reaction between the lead and the sulfur content of the oil takes place quickly and completely with the formation of a precipimm which is removed in any suitable way as by filtration or sedimentation and decantation. The treatment described has been found to remove the sulfur content of the oil very completely so that not even a trace can be detected by ordinary methods. The foregoing step for the removal of the last traces of sulfur from the oil may advantageously be preceded by a treatment of the oil for the removal of the bulk of its sulfur content, for instance, by agitating the 011 with a water solution of a ad compound. If the oil contains a relatively large amount of sulfur a portion of which is removable by the old process a considerable saving in the use of the alcoholic solution for the removal of the last traces of sulfur results.
The oil from which sulfur has been removed may be treated next for the removal of acetylene hydrocarbons. This treatment consists simply in mixing the oil at ordinary atmospheric temperature with an alcoholic solution of a copper compound in quantity just equivalent to the precipitatable acetylene hydrocarbon content thereof and separating the resulting precipitate. A su1t able copper containing solution for use in this step may be prepared by suspending a copper salt, such as the-chlorid, nitrate, or acetate, in alcohol and saturating the mixture with ammonia.
The next step of the complete process for the purification of the oil under consideration is the treatment for the removal of diolefines. This step consists in mixing the oil at ordinary or other suitable temperature with an alcoholic solution of a mercury compound for instance mercuric chlorid, nitrate, or acetate, in quantity only suflicient to precipitate the diolefine hydrocarbon content of the oil. The resulting precipitate which contains the mercury and the diolefines is curdy and preferably is separated from the oil by decantation.
The next step in the process is for the removal of resinous materials. This is accomplished by treating the oil with an alcoholic solution of caustic soda, for instance by agitating the oil with an alcoholic caustic soda solution at atmospheric temperature, and then adding a relatively small amount of water, agitating, and decanting or otherwise separating the clarified oil. The clarified oil may then be washed with water to remove dissolved alcohol therefrom and the alcohol recovered by fractionation of the wash Water and the purified oil is finally steam dis tilled.
The several precipitates formed may if desired be treated by methods known or obvious to a chemist for the recovery therefrom of the precipitating agents and the precipitated materials.
In the foregoing description I have referred to the use of the several precipitating agents or chemicals in quantity only sufficient to accomplish the desired precipitation. This is important not only from the standpoint of economy in the use of the reagents and further in that the contamination of the oil with excess of reagent which would make necessary a purifying step for its removal is avoided, but also, particularly in the step for the removal of diolefines, removal or destruction or undesired conversion of the olefine hydrocarbon content of the oil is avoided. For instance in the sulfur removing step if an excess of the lead precipitating agent is employed the excess or some of it will remain in the oil and necessitate a Washing treatment for its removal. In the diolefine hydrocarbon removing step if an excess of the mercury precipitating agent is used some of the olefine hydrocarbons in the oil may be destroyed by oxidation or converted into undesirable resinous bodies which, as is stated above, are objectionable, due to their umming action, and must be removed, this 0 jectionable feature being in addition to the loss of valuable olefine hydrocarbons. This use of the precipitating agents in quantity only sufficient to accomplish the desired precipitation without contamination of the oil is made possible by the use in accordance with my invention of a mutual solvent or re action medium for the oil and the precipi-' tant because in the presence of such a reaction medium the reaction between the precipitat-.
ing agent and the component of the oil to be precipitated proceeds to'completion quickly without the use of an excess of reagent, The quantities of the reagents necessary in each step are readily determined by'a laboratory titration on a sample of the oil under treatment to the precipitation end point in the known manner.
The procedure described in the foregoing speclfic example is preferred for several reasons, among which may be mentioned the fact that if the sulfur and acetylene hydrocarbon content of the oil are not-removed prior to the diolefine hydrocarbon precipitation they will combine with the mercury compound employed in this step, thus producing a composite precipitate from which the several precipitated components are not readily recoverable. The step by step method is systematic and thorough. owever, it is to be understood that the invention is not limited in this respect. Within the scope of my invention several components of the oil may be precipitated simultaneously by a single precipitating agent or by the use of a mixture of the precipitating agents for the several components or the several components may be precipitated successively by the successive addition of the-several precipitating agents without the separation of the individual precipitates formed.
It is further noted that the invention is not limited to the removal from a hydrocarbon oil of the particular components heretofore referred to excepting as may be required by *the appended claims. The process of my invention may be applied for the removal of any single or any particular group of components, for instance, for the removal of sulfur or acetylene hydrocarbons or diolefines, or resinous matter, or any combination thereof or any other impurity or material in any hydrocarbon oil for the precipitation of which a suitable reagent and reaction medium may be found.
In the appended claims reference is made to the mutual solvent or reaction medium as a solvent for the precipitant which is soluble in the oil. The reference to the solubility of the solvent for the precipitant in the oil is intended to cover any condition of miscibility or of mutual solution as between the oil and the solvent for the precipitant.
I claim:
1. Process of purifying a hydrocarbon oil containing sulfur, diolefine hydrocarbons, acetylene hydrocarbons, olefine hydrocarbons and resinous material which comprises removing the bulk of the sulfur by treating the oil with an aqueous solution of a lead compound, removing the last traces of sulfur from the oil by mixing it with an alcoholic solution of a lead compound and separating the resulting precipitate, removing acetylene hydrocarbons from the oil by mixing it with. an alcoholic solution of a copper compound and separating the'resulting precipitate, removing diolefine hydrocarbons from the oil by mixing it with an alcoholic solution of a mercury compound and separating the resulting precipitate, and removing resinous material from the oil by treatment with an alcoholic solution of caustic soda and then washing with water.
2. Process of purifying hydrocarbon oils which comprises precipitating sulfur therefrom by treatment thereof with a leadcom pound in the presence of a solvent for said lead compound which is soluble in the oil, precipitating diolefine hydrocarbons by treatment with a mercury compound in quantity not substantially in excess of the quantity necessary to precipitate said diolefines in the presence of a solvent for said mercury compound which is soluble in the oil, and thereafter removing resinous material from the oil by treatment with an alcoholic caustic soda solution and washing with water.
3. Process of purifying a hydrocarbon oil containin sulfur, diolefine hydrocarbons, acetylene Iiydrocarbons, olefine hydrocarbons and resinous material which comprises treating the oil for the removal of sulfur compounds therefrom and thereafter removing acetylene hydrocarbons from the oil by mixing it with an alcoholic solution of a copper compound and separating the resulting precipitate, removing diolefine hydrocarbons from the oil by mixing it with an alcoholic solution of a mercury compound and separating the resulting precipitate, and removing resinous material from the oil by treatment with an alcoholic solution of caustic soda and then washing with water.
'4. Process of purifying hydrocarbon oils which comprises treating the oil for the removal of the sulfur content thereof and thereafter precipitating diolefine hydrocarbons by treatment with a mercury compound in quantity not substantially in excess of the quantity necessary to precipitate said diolefines in the presence of a solvent for said mercury compound which is soluble in the oil, and thereafter removing resinous material from the oil by treatment'with an alcoholic caustic soda solution and washin with water.
5. Process of purifying a hydrocarbon oil containing diolefine and acetylene hydrocarbons which comprises removing the acetylene hydrocarbons from the oil by mixing it with an alcoholic solution of a copper compound and separatin the resulting precipitate, and removing the iolefine hydrocarbons from the oil by mixing it with an alcoholic solution of a mercury compound and separating the resulting precipitate.
6. In a process of purifying a hydrocarbon oil the step which comprises removin an impurity of the group consisting of su fur, diolefine hydrocarbons and acetylene hydrocarbons by mixing the oil with an'alcoholic solution of a mercury compound andseparating the resulting precipitate.
7. In a process of purifying a hydrocarbon oil the step which comprises removing diolefine hydrocarbons by mixing the oil with an alcoholic solution of a mercury compound and separating the resulting precipitate.
In testimony whereof, I aflix my signature.
f atmt N0. i.771,350.
CERIIFKQATE 0F CGRRECTION;
July 22, 1930.
ALEXANEEER S. RAMAGE.
it'is hereby certified that the nestze sf the assignee in the above numbered patent was erremiuusiy deem-fixed and specified as "Gyro Process Cerpsration" whereas said name simuid have been described and specified as Gym Process Gnmpany, as stews; by the recerds of assignments in this office; and that the said Letters Pzztsut el e-aid be read with this correction therein that the same may centers: to the; record of the case in the Patent Office.
Signed and sealed this 13th day 0% March, A. D. 1934.
F. M. Hopkins (Seal) Acting Commissioner of Patents.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US670780A US1771350A (en) | 1923-10-25 | 1923-10-25 | Process of refining hydrocarbon oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US670780A US1771350A (en) | 1923-10-25 | 1923-10-25 | Process of refining hydrocarbon oils |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1771350A true US1771350A (en) | 1930-07-22 |
Family
ID=24691839
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US670780A Expired - Lifetime US1771350A (en) | 1923-10-25 | 1923-10-25 | Process of refining hydrocarbon oils |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1771350A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2418183A (en) * | 1944-11-16 | 1947-04-01 | Shell Dev | Prevention of emulsions during extraction of olefins with metal salt solutions |
| US2441400A (en) * | 1943-05-12 | 1948-05-11 | Union Oil Co | Acetylene removal process |
| US2467845A (en) * | 1945-05-12 | 1949-04-19 | Standard Oil Dev Co | Diolefin extraction |
| US2671049A (en) * | 1951-06-30 | 1954-03-02 | Standard Oil Co | Odor improvement of petroleum oils |
| US2744051A (en) * | 1951-08-25 | 1956-05-01 | Universal Oil Prod Co | Treatment of fuel oil with an alkyl pyrrole |
| US2913406A (en) * | 1955-07-27 | 1959-11-17 | Charles O Hoover | Method of preventing corrosion of metallic petroleum refining apparatus and composition therefor |
| US2953611A (en) * | 1955-10-29 | 1960-09-20 | Spengler Gunter | Method and addition compounds for separating olefines from mixtures |
| US2973396A (en) * | 1958-01-30 | 1961-02-28 | Grace W R & Co | Method of purifying diolefins |
-
1923
- 1923-10-25 US US670780A patent/US1771350A/en not_active Expired - Lifetime
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2441400A (en) * | 1943-05-12 | 1948-05-11 | Union Oil Co | Acetylene removal process |
| US2418183A (en) * | 1944-11-16 | 1947-04-01 | Shell Dev | Prevention of emulsions during extraction of olefins with metal salt solutions |
| US2467845A (en) * | 1945-05-12 | 1949-04-19 | Standard Oil Dev Co | Diolefin extraction |
| US2671049A (en) * | 1951-06-30 | 1954-03-02 | Standard Oil Co | Odor improvement of petroleum oils |
| US2744051A (en) * | 1951-08-25 | 1956-05-01 | Universal Oil Prod Co | Treatment of fuel oil with an alkyl pyrrole |
| US2913406A (en) * | 1955-07-27 | 1959-11-17 | Charles O Hoover | Method of preventing corrosion of metallic petroleum refining apparatus and composition therefor |
| US2953611A (en) * | 1955-10-29 | 1960-09-20 | Spengler Gunter | Method and addition compounds for separating olefines from mixtures |
| US2973396A (en) * | 1958-01-30 | 1961-02-28 | Grace W R & Co | Method of purifying diolefins |
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