US2493596A - Process for refining hydrocarbon oils - Google Patents
Process for refining hydrocarbon oils Download PDFInfo
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- US2493596A US2493596A US753579A US75357947A US2493596A US 2493596 A US2493596 A US 2493596A US 753579 A US753579 A US 753579A US 75357947 A US75357947 A US 75357947A US 2493596 A US2493596 A US 2493596A
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- oil
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- impurities
- solvent extraction
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- 239000003921 oil Substances 0.000 title claims description 60
- 229930195733 hydrocarbon Natural products 0.000 title claims description 31
- 150000002430 hydrocarbons Chemical class 0.000 title claims description 31
- 238000000034 method Methods 0.000 title claims description 25
- 239000004215 Carbon black (E152) Substances 0.000 title description 26
- 238000007670 refining Methods 0.000 title description 7
- 239000000126 substance Substances 0.000 claims description 36
- 239000003795 chemical substances by application Substances 0.000 claims description 30
- 239000012535 impurity Substances 0.000 claims description 26
- 238000000638 solvent extraction Methods 0.000 claims description 23
- 239000002904 solvent Substances 0.000 claims description 20
- DAMJCWMGELCIMI-UHFFFAOYSA-N benzyl n-(2-oxopyrrolidin-3-yl)carbamate Chemical compound C=1C=CC=CC=1COC(=O)NC1CCNC1=O DAMJCWMGELCIMI-UHFFFAOYSA-N 0.000 claims description 11
- 230000001376 precipitating effect Effects 0.000 claims description 11
- 239000002480 mineral oil Substances 0.000 claims description 10
- 239000010688 mineral lubricating oil Substances 0.000 claims description 6
- 235000010446 mineral oil Nutrition 0.000 claims description 5
- 239000000470 constituent Substances 0.000 description 14
- 239000000295 fuel oil Substances 0.000 description 11
- 238000011282 treatment Methods 0.000 description 9
- 229910052787 antimony Inorganic materials 0.000 description 8
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 8
- 239000002244 precipitate Substances 0.000 description 7
- 229910052785 arsenic Inorganic materials 0.000 description 6
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 5
- 238000000605 extraction Methods 0.000 description 5
- 150000004820 halides Chemical class 0.000 description 5
- 238000009434 installation Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000011574 phosphorus Substances 0.000 description 5
- 229910052698 phosphorus Inorganic materials 0.000 description 5
- 238000004821 distillation Methods 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 239000010687 lubricating oil Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000010426 asphalt Substances 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- NUMXHEUHHRTBQT-AATRIKPKSA-N 2,4-dimethoxy-1-[(e)-2-nitroethenyl]benzene Chemical compound COC1=CC=C(\C=C\[N+]([O-])=O)C(OC)=C1 NUMXHEUHHRTBQT-AATRIKPKSA-N 0.000 description 1
- 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
- 241000518994 Conta Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- FAPDDOBMIUGHIN-UHFFFAOYSA-K antimony trichloride Chemical compound Cl[Sb](Cl)Cl FAPDDOBMIUGHIN-UHFFFAOYSA-K 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- JMBNQWNFNACVCB-UHFFFAOYSA-N arsenic tribromide Chemical compound Br[As](Br)Br JMBNQWNFNACVCB-UHFFFAOYSA-N 0.000 description 1
- 229940077468 arsenic tribromide Drugs 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 238000011284 combination treatment Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- LIYKJALVRPGQTR-UHFFFAOYSA-M oxostibanylium;chloride Chemical compound [Cl-].[Sb+]=O LIYKJALVRPGQTR-UHFFFAOYSA-M 0.000 description 1
- CFVVSQSFKWLGAX-UHFFFAOYSA-N phenol;propane Chemical compound CCC.OC1=CC=CC=C1 CFVVSQSFKWLGAX-UHFFFAOYSA-N 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- WQYSXVGEZYESBR-UHFFFAOYSA-N thiophosphoryl chloride Chemical compound ClP(Cl)(Cl)=S WQYSXVGEZYESBR-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
- C10G73/00—Recovery or refining of mineral waxes, e.g. montan wax
- C10G73/02—Recovery of petroleum waxes from hydrocarbon oils; Dewaxing of hydrocarbon oils
- C10G73/06—Recovery of petroleum waxes from hydrocarbon oils; Dewaxing of hydrocarbon oils with the use of solvents
-
- 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
- C10G21/00—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
- C10G21/003—Solvent de-asphalting
Definitions
- This invention relates to the art of treating hydrocarbon oils. It pertains more particularly to a process for removing undesirable substances such as ash-forming constituents and/or asphaltic substances from hydrocarbon oils, especially oils of the character of mineral lubricating oils and residual hydrocarbon oils for use as fuel for, e. g., gas turbine installations.
- the asphaltic substances have the drawback in such fuel oil that they greatly increase the viscosity of the oil, so that in general it is necessary to dilute the oil with a considerable proportion of less viscous and more expensive distillate materials.
- oils particularly mineral lubricating oils, containing asphal'tic substances
- certain combinations of extraction agents which bring about the removal by extraction of the asphaltic substances, for example, with the combination propane-phenol (and/or cresol) or with the aid of a combination such as antimony trichloride-ethyl ether, or even with a solvent extraction proportion of liquefied antimony trichloride.
- Application of solvent extraction forthe removal of asphaltic substances from residual oils in the production of cheap fuels is too expensive to be considered.
- solvent extraction with liquefied antimony trichloride to the refining of more valuable lubricating oils is not entirely satisfactory, particularly from the standpoint of economy. 7
- a further object is to provide aprocess wherein asphaltic substances are more economically removed from hydrocarbon oils.
- Another object is to provide a process for readily, economically and effectively removing ash-forming constituents and/or asphaltic substances from heavier hydrocarbon oils, such as residual hydrocarbon oils.
- Still another object is to provide an improved process for the removal of asphaltic substances from mineral lubricating oils.
- the present invention provides an improved process for refining hydrocarbon oils, particularly residual hydrocarbon oils which contain ash-forming constituents and asphaltic substances and hydrocarbon lubricating oils which contain asphaltic substances, which process comprises treating the impurity-containing oil with an added, small amount of one or more of an agent from the halides, oxyhalides and sulfohalides of antimony, arsenic and phosphorus, which agent does not react with the hydrocarbon oil under the conditions of the treatment, there- 'by precipitating the ash-forming constituents and/or the asphaltic substances, and separating the precipitated impurities from the hydrocarbon oil.
- the separated oil fraction may be advantageously further treated as by a solvent extraction process with a selective solvent such as a phenol, furfural, liquid sulfur dioxide, liquefied antimony trichloride, a sulfolane, etc.
- a selective solvent such as a phenol, furfural, liquid sulfur dioxide, liquefied antimony trichloride, a sulfolane, etc.
- such a small quantity of the treating agent may be used as will suflice to practically completely precipitate the ash-forming constituents, but to leave a part of the asphaltic substances dissolved in the oil.
- Examples of substances which maiy-beusedin accordance with the invention as the treating agent are antimony trichloride, arsenic trichlm ride, arsenic tribromide, phosphorus trichloride, phosphorus sulfochloride, antimony pentach10- ride, antimony oxychloride, etc.
- the quantity by weight in which the-treating agents of the invention are added to the hydrocarbon oil depends on, the quantities of ashforming constituents and asphaltic substances oc. curring in the oil to be purified. amounts of not more than about l% by weight of' the oil .to be thus treated, and in many cases not more than by weight of the oil, efiect the required precipitationiof the impurities and refinement of the oil.
- the precipitation and/or coagulation treat.- ment is not confined to any particular temperature or narrow temperature range. Normal or elevated temperatures may be applied. When applying normal or slightly. elevated temperatures the precipitated ash forming constituents and/or asphaltic substances generally'do not settleout readily in the case of relatively viscous oils but may be easily separated from the oil by centrifugation. If, on theother hand, the precipitation is effected at a temperature of from about 150 C. to 250 0., the precipitates obtained will settle fairly quickly and the oil can be easily separated therefrom-by decantation.
- the treating agent used for this purpose may be recovered from the oil by distillation or by shaking the oil with a solvent for the agent, which solvent is at least partially immiscible with the oil.
- the sep: arated solvent solution of the agent may then be separated. by distillation and any of the solvent dissolved in theoil may be separated therefrom by distillation.
- the precipitate When the halides, oxyhalides and sulfohalides of antimony, arsenic and phosphorus'are entrained to any considerable extent by the precipitate separating from the oil, it is in many cases profitable to recover these agents also from the precipitate.
- This may, for example, be effected by distillation under reduced pressure, or the precipitate may be treated with an inert diluent, such as naphtha and/or with a solvent for the agent such as a concentrated aqueous solution of hydrogen chloride, etc..
- the thus p etreated oil may in some case be subjected to a solvent extraction treatment with g a. solvent amount of the same agent, for example, when the agentis antimony chloride.
- a solvent extraction treatment with g a. solvent amount of the same agent, for example, when the agentis antimony chloride.
- the precipitating agent and the selective solvent are not the same, it often is not necessary to remove the precipitating agent remaining in the oil before effecting the solvent extraction unless the solvent is reactive with said agent, which, in general, is not so.
- the agent and solvent are different the small amount of agent dissolved in the oil enhances the selectivity of the solvent toward the various types of hydrocarbons present in the 011.
- both the raflinate phase and the extract phase are liberated of the added substance (solvent) or substances (solvent and agent). It will generally be deemed desirable to recover the solvent and agent separately for the treatment of a fresh quantity of oil.
- solvent substance
- agent substances
- E tdmple II AVenezuelan oil residue-obtained by distilling ff from a Chinese oilthe constituents boiling above about-380 C. (atmospheric pres, sure) and which residue had an asphaltene content of 8.8% by weight, wasthoroughly mixed at .20. C. with 3% byweight of antimony ri. chloride and then was allowed to stand for half an. our.
- h oil was, separated fr m the e ment obtained by de entation, t s ill conta n d 0.5% by weigh of a p e te es and was subse quently xtra ted in ooun s ourrent with 40% by volum o liquefi d ant mony tr ohloride at C. n: pparatus. rovided. vw tl-ithis-1e mix ineand settl ne tenks. The.
- W thout applyin a pretreatment as described above, a similar resultwith a. oo lntercurrent extraction in the same apparatus and under the same onditi ns waso tainede y-when the es? traction had been effected with about 75% by volume of antimony trichloride.
- the combination process represented an economy of 35 volumes of SbC13 extractive solvent out of '75 volumes, for a pretreatment outlay of only three volumes of SbCls.
- the present invention provides an improved process for the removal of ash-forming constituents and/or asphaltic substances from hydrocarbon oils.
- the invention is of particular utility in refining residual hydrocarbon oils so that they may be used advantageously, alone or in mixtures with a content of at least 50% by weight of such residual oils, the rest being made up of, for instance, mineral oil distillates, synthetically prepared ash-free types of oil, benzene, etc., as fuel for operating gas turbine installations.
- the embodiment of the invention wherein a pretreatment as described herein is combined with a subsequent solvent extraction operation has utility as a process of greater economy for the refining and production of lubricating oils.
- a process for removing ash-forming impurities from residual hydrocarbon fuel oils which process comprises treating said impurity containing fuel oils with a minor but impurityprecipitating amount not more than about 10% by weight of a halide agent selected from the group consisting of the trihalides of antimony, arsenic and phosphorus and mixtures thereof, as the active impurity-precipitating agent, under conditions of temperature, time and proportions to precipitate a substantial portion of said ashforming constituents, and separating the resulting precipitated impurities from an improved fuel oil.
- a halide agent selected from the group consisting of the trihalides of antimony, arsenic and phosphorus and mixtures thereof, as the active impurity-precipitating agent
- a process for removing ash-forming impurities from residual hydrocarbon fuel oils containing also asphaltic substances comprises treating said impurity-containing fuel oils with a minor but impurity-precipitating amount not more than about 10% by weight of a halide agent selected from the group consisting of the trihalides of antimony, arsenic and phosphorus and mixtures thereof, as the active impurity-precipitating agent, at a temperature up to about 250 C., and with proportions selected to selectively precipitate substantially completely said ash-forming impurities while leaving a substantial portion of the asphaltic substances dissolved in said oil, and separating the resulting precipitated impurities from an improved fuel oil.
- a halide agent selected from the group consisting of the trihalides of antimony, arsenic and phosphorus and mixtures thereof, as the active impurity-precipitating agent
- a process for removing ash-forming impurities from residual hydrocarbon fuel oils containing also asphaltic substances comprises treating said impurity-containing fuel oils with a minor but impurity-precipitatin amount not more than about 10% by weight of antimony trichloride, as the active impurity-precipitating agent, at a temperature up to about 250 C., and with proportions selected to selectively precipitate substantially completely said ash-forming impurities while leaving a substantial portion of the asphaltic substances dissolved in said oil, and separating the resulting precipitated impurities from an improved fuel oil.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Patented Jan. 3, i950 PROCESS FOR REFINING HYDROCARBON OILS Gerrit Hendrik Reman, Amsterdam, Netherlands, assignor to Shell Development Company, San Francisco, Calif., a corporation of Delaware No Drawing. Application June 9, 1947,
Serial No. 753,579
In the Netherlands June 20, 1946 6 Claims.
This invention relates to the art of treating hydrocarbon oils. It pertains more particularly to a process for removing undesirable substances such as ash-forming constituents and/or asphaltic substances from hydrocarbon oils, especially oils of the character of mineral lubricating oils and residual hydrocarbon oils for use as fuel for, e. g., gas turbine installations.
The use of residual hydrocarbon oils, either alone or mixed with, for example, oil distillates, as fuel for, e. g. gas turbineinstallations, is attractive for economical reasons. The ash-forming constituents, however, and to a smaller degree also the asphaltic substances, generally occurring in residual hydrocarbon oils, constitute a drawback to the use of the latter as fuel oil for this purpose. The ash-forming constituents which, it will be understood, are inorganic-containing substances and form non-volatile mineral or inorganic compounds upon combustion, have a fouling effect on the installations in which said oils are used. As a result,'the installation soon begins to operate less smoothly and too soon for economical reasons the operation must be stopped for a thorough cleaning of the installation.
The asphaltic substances have the drawback in such fuel oil that they greatly increase the viscosity of the oil, so that in general it is necessary to dilute the oil with a considerable proportion of less viscous and more expensive distillate materials.
It has already been proposed to refine oils, particularly mineral lubricating oils, containing asphal'tic substances with certain combinations of extraction agents which bring about the removal by extraction of the asphaltic substances, for example, with the combination propane-phenol (and/or cresol) or with the aid of a combination such as antimony trichloride-ethyl ether, or even with a solvent extraction proportion of liquefied antimony trichloride. Application of solvent extraction forthe removal of asphaltic substances from residual oils in the production of cheap fuels is too expensive to be considered. Furthermore, even the application of solvent extraction with liquefied antimony trichloride to the refining of more valuable lubricating oils is not entirely satisfactory, particularly from the standpoint of economy. 7
It is a principal object, therefore, of this invention to provide an improved process for treating heavier hydrocarbon oils. A further object is to provide aprocess wherein asphaltic substances are more economically removed from hydrocarbon oils. Another object is to provide a process for readily, economically and effectively removing ash-forming constituents and/or asphaltic substances from heavier hydrocarbon oils, such as residual hydrocarbon oils. Still another object is to provide an improved process for the removal of asphaltic substances from mineral lubricating oils. These objects will be more clearly understood and other objects will be evident from the detailed description of the invention.
Now, in accordance with the present invention, it has been found that the above and other objects may be realized by a process wherein a heavier hydrocarbon oil which contains undesirable impurities such as ash-forming constituents and/or asphaltic substances is treated with a minor but effective precipitating and/or coagulating amount of a precipitating and/0r coagulating agent for said impurities followed by separation of the resulting precipitated or coagulated matter'together with said agent. In some cases, this treament may be combined with other subsequent treatments to provide advantageous combination treatments or processes wherein the above described treatment is in the nature of a pretreatment.
Generally described, the present invention provides an improved process for refining hydrocarbon oils, particularly residual hydrocarbon oils which contain ash-forming constituents and asphaltic substances and hydrocarbon lubricating oils which contain asphaltic substances, which process comprises treating the impurity-containing oil with an added, small amount of one or more of an agent from the halides, oxyhalides and sulfohalides of antimony, arsenic and phosphorus, which agent does not react with the hydrocarbon oil under the conditions of the treatment, there- 'by precipitating the ash-forming constituents and/or the asphaltic substances, and separating the precipitated impurities from the hydrocarbon oil. With the application of this treatment to a hydrocarbon lubricating oil fraction, the separated oil fraction may be advantageously further treated as by a solvent extraction process with a selective solvent such as a phenol, furfural, liquid sulfur dioxide, liquefied antimony trichloride, a sulfolane, etc. In that case, the combination of the first or pretreatment operation with the subsequent refining treatment as by solvent extraction materially decreases the amount of selective solvent required in the solvent extraction to an extent that there are realized economies in the overall process over the required solvent extraction when that is used alone without the advantages of the described pretreatment. Thus, when ficient antimony trichloride is utilized alone in the extraction operation to produce an oil railinate of similar quality.
In some applications of the present invention such as to residual hydrocarbon oils, such a small quantity of the treating agent may be used as will suflice to practically completely precipitate the ash-forming constituents, but to leave a part of the asphaltic substances dissolved in the oil.
Examples of substances which maiy-beusedin accordance with the invention as the treating agent are antimony trichloride, arsenic trichlm ride, arsenic tribromide, phosphorus trichloride, phosphorus sulfochloride, antimony pentach10- ride, antimony oxychloride, etc.
The quantity by weight in which the-treating agents of the invention are added to the hydrocarbon oil depends on, the quantities of ashforming constituents and asphaltic substances oc. curring in the oil to be purified. amounts of not more than about l% by weight of' the oil .to be thus treated, and in many cases not more than by weight of the oil, efiect the required precipitationiof the impurities and refinement of the oil.
The precipitation and/or coagulation treat.- ment is not confined to any particular temperature or narrow temperature range. Normal or elevated temperatures may be applied. When applying normal or slightly. elevated temperatures the precipitated ash forming constituents and/or asphaltic substances generally'do not settleout readily in the case of relatively viscous oils but may be easily separated from the oil by centrifugation. If, on theother hand, the precipitation is effected at a temperature of from about 150 C. to 250 0., the precipitates obtained will settle fairly quickly and the oil can be easily separated therefrom-by decantation.
After removal of the precipitated ash-forming constituents and asphaltic-suhstances the treating agent used for this purpose may be recovered from the oil by distillation or by shaking the oil with a solvent for the agent, which solvent is at least partially immiscible with the oil. The sep: arated solvent solution of the agent may then be separated. by distillation and any of the solvent dissolved in theoil may be separated therefrom by distillation.
When the halides, oxyhalides and sulfohalides of antimony, arsenic and phosphorus'are entrained to any considerable extent by the precipitate separating from the oil, it is in many cases profitable to recover these agents also from the precipitate. This may, for example, be effected by distillation under reduced pressure, or the precipitate may be treated with an inert diluent, such as naphtha and/or with a solvent for the agent such as a concentrated aqueous solution of hydrogen chloride, etc.. e
' In the event the foregoing described treatment 'to precipitate impurities is applied to a lubrireating oilfraction such as a hydrocarbon distillate; the thus p etreated oil may in some case be subjected to a solvent extraction treatment with g a. solvent amount of the same agent, for example, when the agentis antimony chloride. In that event the a ent remaining in the l after the first or pretreatment need not b recover d therefromv prior to the solvent extraction. Even V In general,
when the precipitating agent and the selective solvent are not the same, it often is not necessary to remove the precipitating agent remaining in the oil before effecting the solvent extraction unless the solvent is reactive with said agent, which, in general, is not so. In some cases where the agent and solvent are different the small amount of agent dissolved in the oil enhances the selectivity of the solvent toward the various types of hydrocarbons present in the 011.
After the extraction proper has been carried out, both the raflinate phase and the extract phase are liberated of the added substance (solvent) or substances (solvent and agent). It will generally be deemed desirable to recover the solvent and agent separately for the treatment of a fresh quantity of oil. The most suitable meth- To a ol n residue; 1. e. a r idue fr m Venezuelan oil, there was added 3% by weight of SbCh at 200 C. and. the mass was kept at this temperature for half an hour. The oil, formin e pp r l r, w then de nted fr m he pie oipitate which had formed and s t ede SbCIa w covered fro theoil'by first dilu ing h l tt r wi h benz neand then shakin it o t with a hydrochloric. acid s lution. The two liqu d layers thus formed were separat d and he h n zene was distilled off fromthe oil layer. As a re sult of the treatment the ashecontent of the Colon residue was lower d fromv a value of 1 6% by weight to a valueless than 0.01% by weight; the asphaltene content was lowered from 85% by weight to a value of only 0.5% by weigh Practically the same results were obtained by reating another sample of thesame res du with y weight of AsB -s instead of an equal quan ity o 510013, the other conditions. ope ati ns, tc.
being the same.
E tdmple II AVenezuelan oil residue-obtained by distilling ff from a Venezu lan crude oilthe constituents boiling above about-380 C. (atmospheric pres, sure) and which residue had an asphaltene content of 8.8% by weight, wasthoroughly mixed at .20. C. with 3% byweight of antimony ri. chloride and then was allowed to stand for half an. our. h oil was, separated fr m the e ment obtained by de entation, t s ill conta n d 0.5% by weigh of a p e te es and was subse quently xtra ted in ooun s ourrent with 40% by volum o liquefi d ant mony tr ohloride at C. n: pparatus. rovided. vw tl-ithis-1e mix ineand settl ne tenks. The. reffinete phase, aft r b ng freed fr mantimony tr chlorid c n-- sisted of an oil with a ViSCOSity-Esg 17.51, a viso s t d of 97 ands Ce redsonw r on fleme of 0.75.
W thout applyin a pretreatment as described above, a similar resultwith a. oo lntercurrent extraction in the same apparatus and under the same onditi ns waso tainede y-when the es? traction had been effected with about 75% by volume of antimony trichloride.
Thus, the combination process represented an economy of 35 volumes of SbC13 extractive solvent out of '75 volumes, for a pretreatment outlay of only three volumes of SbCls.
Thus, it is seen that the present invention provides an improved process for the removal of ash-forming constituents and/or asphaltic substances from hydrocarbon oils. The invention is of particular utility in refining residual hydrocarbon oils so that they may be used advantageously, alone or in mixtures with a content of at least 50% by weight of such residual oils, the rest being made up of, for instance, mineral oil distillates, synthetically prepared ash-free types of oil, benzene, etc., as fuel for operating gas turbine installations. Furthermore, the embodiment of the invention wherein a pretreatment as described herein is combined with a subsequent solvent extraction operation has utility as a process of greater economy for the refining and production of lubricating oils.
I claim as my invention:
1. In a process for the refinement of mineral lubricating oils which contain impurities of the character of asphaltic substances, wherein the mineral oils are subjected to solvent extraction with a selective solvent for various hydrocarbons present therein, the improvement which comprises preceding said solvent extraction by treating said mineral oil containing the asphaltic substances with a minor but asphalt-precipitating amount up to about by weight of antimony trichloride as sole active precipitating agent under conditions to precipitate at least a substantial portion of said impurities, and separating the resulting precipitated impurities from the oil prior to the solvent extraction operation.
2. In a process for the refinement of mineral lubricating oils which contain impurities of the character of asphaltic substances, wherein the mineral oils are subjected to solvent extraction with liquefied antimony trichloride as a selective solvent for various hydrocarbons present therein, the improvement which comprises preceding said solvent extraction by treating said mineral oil containing the asphaltic substances with a minor but asphalt-precipitating amount up to about 10% by weight of antimony trichloride as sole active precipitating agent at a temperature of from about 150 C. to about 250 0., thereby precipitating at least a substantial portion of said impurities, and separating the resulting precipitated impurities from the oil prior to the solvent extraction operation.
3. In a process for the refinement of mineral oils which contain asphaltic substances, wherein the mineral oils are subjected to solvent extraction with a selective solvent for various hydrocarbons present therein, the improvement which comprises preceding said solvent extraction by treating said mineral oil containing the asphaltic substances with a minor but asphalt precipitating amount not more than about 10% by weight of a halide agent selected from the group consisting of the trihalides of antimony, arsenic 6 and phosphorus and mixtures thereof, as the sole active precipitating agent, under conditions to precipitate at least a substantial portion of said asphalt substances, and separating the resulting precipitated asphaltic substances from the oil prior to the solvent extraction operation.
4. A process for removing ash-forming impurities from residual hydrocarbon fuel oils, which process comprises treating said impurity containing fuel oils with a minor but impurityprecipitating amount not more than about 10% by weight of a halide agent selected from the group consisting of the trihalides of antimony, arsenic and phosphorus and mixtures thereof, as the active impurity-precipitating agent, under conditions of temperature, time and proportions to precipitate a substantial portion of said ashforming constituents, and separating the resulting precipitated impurities from an improved fuel oil.
5. A process for removing ash-forming impurities from residual hydrocarbon fuel oils containing also asphaltic substances, which process comprises treating said impurity-containing fuel oils with a minor but impurity-precipitating amount not more than about 10% by weight of a halide agent selected from the group consisting of the trihalides of antimony, arsenic and phosphorus and mixtures thereof, as the active impurity-precipitating agent, at a temperature up to about 250 C., and with proportions selected to selectively precipitate substantially completely said ash-forming impurities while leaving a substantial portion of the asphaltic substances dissolved in said oil, and separating the resulting precipitated impurities from an improved fuel oil.
6. A process for removing ash-forming impurities from residual hydrocarbon fuel oils containing also asphaltic substances, which process comprises treating said impurity-containing fuel oils with a minor but impurity-precipitatin amount not more than about 10% by weight of antimony trichloride, as the active impurity-precipitating agent, at a temperature up to about 250 C., and with proportions selected to selectively precipitate substantially completely said ash-forming impurities while leaving a substantial portion of the asphaltic substances dissolved in said oil, and separating the resulting precipitated impurities from an improved fuel oil.
GERRIT HENDRIK REMAN.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,601,753 Hellthaler Oct. 5, 1926 1,823,558 Burke Sept. 15, 1931 2,176,884 Butz Oct. 24, 1939 2,246,257 Kohn June 1'7, 1941 2,305,248 Fleer et al. Dec. 15, 1942 2,322,083 van der Plas June 15, 1943 2,339,786 Larsen et a1. Jan. 25, 1944
Claims (1)
1. IN A PROCESS FOR THE REFINEMENT OF MINERAL LUBRICATING OILS WHICH CONTAIN IMPURITIES OF THE CHARACTER OF ASPHALTIC SUBSTANCES, WHEREIN THE MINERAL OILS ARE SUBJECTED TO SOLVENT EXTRACTION WITH A SELECTIVE SOLVENT FOR VARIOUS HYDROCARBONS PRESENT THEREIN, THE IMPROVEMENT WHICH COMPRISES PRECEDING SAID SOLVENT EXTRACTION BY TREATING SAID MINERAL OIL CONTAINING THE ASPHALTIC SUBSTANCES WITH A MINOR BUT ASPHALT-PRECIPITATING AMOUNT UP TO ABOUT 10% BY WEIGHT OF ANTIMONY TRICHLORIDE AS SOLE ACTIVE PRECIPITATING AGENT UNDER CONDITIONS TO PRECIPITATE AT LEAST A SUBSTANTIAL PORTION OF SAID IMPURITIES, AND SEPARATING THE RESULTING PRECIPITATED IMPURITIES FROM THE OIL PRIOR TO THE SOLVENT EXTRACTION OPERATION.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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NL2493596X | 1946-06-20 |
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US2493596A true US2493596A (en) | 1950-01-03 |
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US753579A Expired - Lifetime US2493596A (en) | 1946-06-20 | 1947-06-09 | Process for refining hydrocarbon oils |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2588346A (en) * | 1949-10-22 | 1952-03-11 | Houdry Process Corp | Refining gasoline and petroleum oils with aqueous antimony trichloride |
US3483118A (en) * | 1968-04-29 | 1969-12-09 | Universal Oil Prod Co | Hydrorefining a hydrocarbonaceous charge stock with a molten lewis acid and molybdenum sulfide |
US3483117A (en) * | 1968-04-29 | 1969-12-09 | Universal Oil Prod Co | Hydrorefining of metal-containing black oils with a molten lewis acid and a molybdenum halide |
US20080251418A1 (en) * | 2007-04-06 | 2008-10-16 | Manuel Anthony Francisco | Upgrading of petroleum resid, bitumen, shale oil, and other heavy oils by the separation of asphaltenes and/or resins therefrom by electrophilic aromatic substitution |
US9222147B2 (en) | 2012-01-12 | 2015-12-29 | Nichromet Extraction Inc. | Method for selective precipitation of iron, arsenic and antimony |
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US1601753A (en) * | 1926-10-05 | Theqdor hellt-h aler | ||
US1823558A (en) * | 1926-09-22 | 1931-09-15 | Combustion Utilities Corp | Purification of tar acid-bearing oils |
US2176884A (en) * | 1937-09-23 | 1939-10-24 | Atlantic Refining Co | Process for producing an improved lubricating oil |
US2246257A (en) * | 1938-07-02 | 1941-06-17 | Shell Dev | Separation of organic mixtures |
US2305248A (en) * | 1941-11-25 | 1942-12-15 | Shell Dev | Process for the recovery of antimony trichloride |
US2322083A (en) * | 1938-12-12 | 1943-06-15 | Shell Dev | Extraction process |
US2339786A (en) * | 1942-11-30 | 1944-01-25 | Shell Dev | Refining of lubricating oils |
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US1601753A (en) * | 1926-10-05 | Theqdor hellt-h aler | ||
US1823558A (en) * | 1926-09-22 | 1931-09-15 | Combustion Utilities Corp | Purification of tar acid-bearing oils |
US2176884A (en) * | 1937-09-23 | 1939-10-24 | Atlantic Refining Co | Process for producing an improved lubricating oil |
US2246257A (en) * | 1938-07-02 | 1941-06-17 | Shell Dev | Separation of organic mixtures |
US2322083A (en) * | 1938-12-12 | 1943-06-15 | Shell Dev | Extraction process |
US2305248A (en) * | 1941-11-25 | 1942-12-15 | Shell Dev | Process for the recovery of antimony trichloride |
US2339786A (en) * | 1942-11-30 | 1944-01-25 | Shell Dev | Refining of lubricating oils |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2588346A (en) * | 1949-10-22 | 1952-03-11 | Houdry Process Corp | Refining gasoline and petroleum oils with aqueous antimony trichloride |
US3483118A (en) * | 1968-04-29 | 1969-12-09 | Universal Oil Prod Co | Hydrorefining a hydrocarbonaceous charge stock with a molten lewis acid and molybdenum sulfide |
US3483117A (en) * | 1968-04-29 | 1969-12-09 | Universal Oil Prod Co | Hydrorefining of metal-containing black oils with a molten lewis acid and a molybdenum halide |
US20080251418A1 (en) * | 2007-04-06 | 2008-10-16 | Manuel Anthony Francisco | Upgrading of petroleum resid, bitumen, shale oil, and other heavy oils by the separation of asphaltenes and/or resins therefrom by electrophilic aromatic substitution |
US9222147B2 (en) | 2012-01-12 | 2015-12-29 | Nichromet Extraction Inc. | Method for selective precipitation of iron, arsenic and antimony |
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