US1962698A - Refining liquid hydrocarbons - Google Patents
Refining liquid hydrocarbons Download PDFInfo
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- US1962698A US1962698A US551166A US55116631A US1962698A US 1962698 A US1962698 A US 1962698A US 551166 A US551166 A US 551166A US 55116631 A US55116631 A US 55116631A US 1962698 A US1962698 A US 1962698A
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- United States
- Prior art keywords
- hydrocarbon
- treatment
- refining
- oil
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- 229930195733 hydrocarbon Natural products 0.000 title description 58
- 150000002430 hydrocarbons Chemical class 0.000 title description 58
- 238000007670 refining Methods 0.000 title description 43
- 239000007788 liquid Substances 0.000 title description 15
- 239000004215 Carbon black (E152) Substances 0.000 description 46
- 239000003795 chemical substances by application Substances 0.000 description 37
- 239000003921 oil Substances 0.000 description 32
- 238000000034 method Methods 0.000 description 22
- 239000000203 mixture Substances 0.000 description 20
- 229920000642 polymer Polymers 0.000 description 20
- 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 16
- 229910052708 sodium Inorganic materials 0.000 description 16
- 239000011734 sodium Substances 0.000 description 16
- 229910052751 metal Inorganic materials 0.000 description 15
- 239000002184 metal Substances 0.000 description 15
- 229910052783 alkali metal Inorganic materials 0.000 description 11
- 150000001340 alkali metals Chemical class 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- 239000006227 byproduct Substances 0.000 description 9
- 239000010802 sludge Substances 0.000 description 8
- 238000001914 filtration Methods 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920002959 polymer blend Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- JGSARLDLIJGVTE-UHFFFAOYSA-N 3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid Chemical compound O=C1N2C(C(O)=O)C(C)(C)SC2C1NC(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 239000002199 base oil Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 229910000286 fullers earth Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/02—Non-metals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G19/00—Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/04—Metals, or metals deposited on a carrier
Definitions
- An object of this invention is to provide a method for refining hydrocarbons by treatment with a metallic substance whereby the treating agent may be economically land substantially completely utilized.
- a further object is to provide such a process which is applicable to the refining of hydrocarbons having relatively high viscosities as well as the lighter hydrocarbons.
- two-stage refining process I mean a process for refining hydrocarbon wherein the hydrocarbon is first treated with a relatively small amount of refining agent whereby the amount of agent added is substantially entirely consumed and the hydrocarbon is only partially refined, first stage treatment) then this partially refined hydrocarbon, after removal of insoluble treatment by-product,
- the novel combination of such processes according to my invention comprises using the mixture of unreacted refining agent and insoluble treatment byproduct resulting from the second stage of a two-stage process as treating agent in a singlestage process and then using the insoluble material recovered from the single-stage process, which material comprises treatment by-products mixed with relatively small amounts of refining (Cl. IBG-23) agent, as treating agent in the first stage of a succeeding two-stage process.
- the drawing is a diagrammatic .representation of one form of my invention, showing the fio'w of materials through the various steps ofl the process.
- the hydrocarbon to be refined is treated by agitating it preferably at a temperature of from F15-275 C., .with a sludge consisting of alkali metal and treatment byproducts from a prior operation.
- the amount of sludge used is so adjusted that by this treatment substantially all the metal is reacted and the hydrocarbon is only partially refined.
- the sludge is then removed and the hydrocarbon isl subjected to the second stage treatment, which consists in treating ⁇ it with a great excess o1' alkali metal. After the desired degree of refinement has been obtained, the refined hydrocarbon is filtered off.
- the remaining sludge, containing a considerable excess of refining agent, is used as treating agent in a single-stage treatment of a fresh batch of hydrocarbon, which treatment consists in agitating the sludge with the hydrocarbon, preferably at 175-2'75u C., until the desired degree of refinement is obtained.
- the ratio of hydrocarbon to sludge in this single stage treatment must be such that there is an excess of alkali metal over that which will react in producing the desired refinement.
- the sludge recovered by filtration from the single stage treatment contains a relatively low proportion of unreacted metal and is used as refining agent in the first stage of the two-stage treatment of fresh hydrocarbon previously described.
- the partially refined oil is treated with excess rening agent, drawn from the refining agent supply (9), in the second-stage treatment (10).
- the mixture passes from this operation to filter II and the refined oil there separated is transmitted to refined oil storage (12).
- the mixture of polymer and unreacted refining agent separated in filter II is sent to the singlestage treatment (1) where it is used to treat fresh oil drawn from the oil supply (6); and the cycle is vthen repeated.
- the amount of by-product formed and the Viscosity of the hydrocarbon are such that the refining agent is rapidly fouled and is consequently not completely consumed in the first stage of a two-stage treatment.
- This difficulty is avoided by sub-dividing the first stage intov a plurality of treating operations. In each operation a fraction of the amount of refining agent sludge desired in the rst stage is added. After each such fraction has been substantially entirely consumed, insoluble by-product is removed and treatment is continued with the next fraction of refining agent. In this way substantially all of the refining agent is consumed in the first stage treatment.
- barrel is used to designate a unit of 42 gallons.
- Example An acid refined, asphalt base oil was further refined by the process illustrated diagrammatically by the drawing.
- a quantity of insoluble residue, obtained by filtration of the mixture from a previous single-stage treatment of the same oil, containing 18.7% of metallic sodium was mixed with untreated oil in the proportion of 82.25 lbs. of residue. per barrel of oil, corresponding to about 7 lbs. of metallic sodium per barrel of oil and the mixture was agitated at 215-225 C. until tests showed that substantially no metallic sodium remained. This required about 12 hours.
- the mixture was then filtered and the residue, consisting of insoluble polymer and some oil, was discarded.
- the filtrate, consisting of partially refined oil was agitated at 215-225 C., for '7l/2 hours with 24.5 lbs.
- Such dilution may be made at any Characteristics Befflrlt'eat' After treatment Neutralization N o 0.00 0.00 oqior N.P.A..No 2 1 85 Color Saybolt +18 ("Prirne whiteu Sligh oxidation No; 14. 1 1. 7 Steam emulsion N o 200 15 Viscosity at F. 1 50 sec 146 sec. Flush point 325 F 330 F. Fire point 365 370 F. 90
- the hydrocarbon to be refined may be previously treated by any known process; for instance, treatment with sulfuric acid, fullers earth, aluminum chloride, or other known refining agent. Such pre-treatment, preceding refining with metallic refining agent is often desirable because it decreases the amount of Ametal consumed.
- the invention is also not restricted to any particular means of contacting the hydrocarbon with the-refining agent.
- My invention may be used to refine any hydrocarbon material in liquid state, including solutions of hydrocarbons. It is especially adapted for the treatment of petroleum hydrocarbons, regardless of their source or previous treatment.
- lighter grades of such hydrocarbons such as gasoline'and kerosene and is particularly adapted for refining hydrocarbons of relatively-high viscosity, such as lubricating oils.
- oil and hydrocarbon oil mean a liquid hydrocarbon material having an S. U. V. viscosity of 50 seconds or more at F.
- reactive metal is used in the claims to mean a metallic rening agent capable of chemically reacting with the constituents and impurities of the hydrocarbon or hydrocarbon oil treated therewith.
- polymer is used in the claims to designate the insoluble treatment by-products formed during the treatment of a liquid hydrocarbon material with reactive metal, as defined above.
- a cyclic process for refining liquid hydrocarbons comprising treating said liquid With alkali metal-polymer mixture at a temperature above the melting point of the alkali metal until substantially complete consumption of said metal is obtained, removing polymer, completing the reining of said liquid by treating with a fresh supply of the alkali metal in large excess, separating refined liquid, utilizing the recovered metalpolymer mixture for complete refinement of an amount of untreated liquid hydrocarbon insufficient to use up the molten alkali metal in said mixture, separating rened liquid, and utilizing the residual metal-polymer mixture and a new batch of liquid to renew the cycle.
- a process for rening a liquid hydrocarbon comprising agitating a mixture of polymer and alkali metal recovered from a previous rening operation with said hydrocarbon at 10G-275 C. until the metal is substantially entirely consumed,
- a process for rening a liquid hydrocarbon comprising agitating a mixtureof polymer and sodium recovered from a previous refining operation with said hydrocarbon at 10D-275 C. until the sodium is substantially entirely consumed, filtering to remove partially refined hydrocarbon from polymer, agitating said partially refined hydrocarbon with a large excess of sodium at 10U-275 C. until the desired degree of retement is obtained, ltering .to remove a mixture of polymer and unreacted metal from rened hydro- 100 carbon, agitating said separated mixture' at 1D0-275" C.
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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
June 12, 1934.
R. S. VOSE REFINING LIQUID HYDROCARBONS Filed July 16, 1931 r- UPPLY fF//WNG HGH/V7 9: POLY/17E@ POLY/vf? 0mm/90 8 & POLY/Vfl? BEF/N50 /L /2 @5F/M50 o/L 3 Ricwwd IN VEV TOR.
A TTORNE Y Patented .lune 12, 'i934 STATES maar 1,962,698 REFINING LIQUID HYDrtooAmsoNs Application July 16, 1931, Serial N0. 551,166
3 Claims.'
This invention relates to the refining of hydrocarbon materials, and more particularly to refining by metallic agents.
Various metals, including the alkali metals,
5 have been used or proposed as rening agents for hydrocarbon materials. During the treatment of hydrocarbons by sodium for example, some polymerization of certain constituents takes place. Some of these polymers may be soluble in the hydrocarbon and cause no difficulty, other polymers however, separate out as more or less sticky, oily masses which contaminate the solid treating agent, such as sodium. For effective treatment with such metals as sodium it is preferable to use considerable excesses of metal at the end of the refining period, this excess of sodium can be removed from the oil mixed with the solid polymer, but the recovery of the metal from the contaminating polymer is diicult.
An object of this invention is to provide a method for refining hydrocarbons by treatment with a metallic substance whereby the treating agent may be economically land substantially completely utilized. A further object is to provide such a process which is applicable to the refining of hydrocarbons having relatively high viscosities as well as the lighter hydrocarbons.
Other objects will be hereinafter apparent.
These objects are accomplished by a novel combination of a two-stage refining process and a single-stage refining process. By two-stage refining process, I mean a process for refining hydrocarbon wherein the hydrocarbon is first treated with a relatively small amount of refining agent whereby the amount of agent added is substantially entirely consumed and the hydrocarbon is only partially refined, first stage treatment) then this partially refined hydrocarbon, after removal of insoluble treatment by-product,
is treated with an excess of refining agent (second stage) until the desired degree of refinement is obtained. By single stage refining process, I mean a single treatment of hydrocarbon material with excess of refining agent until the desired refinement is obtained. The novel combination of such processes according to my invention comprises using the mixture of unreacted refining agent and insoluble treatment byproduct resulting from the second stage of a two-stage process as treating agent in a singlestage process and then using the insoluble material recovered from the single-stage process, which material comprises treatment by-products mixed with relatively small amounts of refining (Cl. IBG-23) agent, as treating agent in the first stage of a succeeding two-stage process.
The drawing is a diagrammatic .representation of one form of my invention, showing the fio'w of materials through the various steps ofl the process.
One method of carrying out my invention will be described with reference to the use'of alkali metal as refining agent. The hydrocarbon to be refined is treated by agitating it preferably at a temperature of from F15-275 C., .with a sludge consisting of alkali metal and treatment byproducts from a prior operation. The amount of sludge used is so adjusted that by this treatment substantially all the metal is reacted and the hydrocarbon is only partially refined. The sludge is then removed and the hydrocarbon isl subjected to the second stage treatment, which consists in treating `it with a great excess o1' alkali metal. After the desired degree of refinement has been obtained, the refined hydrocarbon is filtered off. -The remaining sludge, containing a considerable excess of refining agent, is used as treating agent in a single-stage treatment of a fresh batch of hydrocarbon, which treatment consists in agitating the sludge with the hydrocarbon, preferably at 175-2'75u C., until the desired degree of refinement is obtained. The ratio of hydrocarbon to sludge in this single stage treatment must be such that there is an excess of alkali metal over that which will react in producing the desired refinement. The sludge recovered by filtration from the single stage treatment contains a relatively low proportion of unreacted metal and is used as refining agent in the first stage of the two-stage treatment of fresh hydrocarbon previously described.
The above described process may be more fully understood by reference to the drawing, which shows, by means of arrows, flow of ymaterials 5 through the various steps. The mixture of refined oil, polymer and unreacted treating agent from the single stage treatment (1) is passed to filter III where the refined oil is separated and passed to the refined Voil storage-(3). The polymer, containing unreacted refining agent (4),'ls sent to the first-stage treatment (5), where it is mixed with oil from the oil supply (6). After the first-stage treatment is completed, the mixture is filtered in filter vl2 where the partially refined oil is separated from the insoluble polymer (8), which contains substantially no refining agent and is discarded. The partially refined oil is treated with excess rening agent, drawn from the refining agent supply (9), in the second-stage treatment (10). The mixture passes from this operation to filter II and the refined oil there separated is transmitted to refined oil storage (12). The mixture of polymer and unreacted refining agent separated in filter II is sent to the singlestage treatment (1) where it is used to treat fresh oil drawn from the oil supply (6); and the cycle is vthen repeated.
The optimum proportion of refining agent to use in the second-stage treatment and the amount of hydrocarbon which can be emciently treated in the single-stage treatment will be found to vary somewhat according to the nature of the hydrocarbon being treated and may be determined by trial runs. These quantities also depend on the desired degree of refinement which must be likewise determined. The temperature to be maintained in the various treating operations should be above the melting point of the refining agent. For treating hydrocarbons having relatively high viscosities, for instance lubricating oils, I prefer to maintain the treatment temperature at 17T-275 C.
In some cases the amount of by-product formed and the Viscosity of the hydrocarbon are such that the refining agent is rapidly fouled and is consequently not completely consumed in the first stage of a two-stage treatment. This difficulty is avoided by sub-dividing the first stage intov a plurality of treating operations. In each operation a fraction of the amount of refining agent sludge desired in the rst stage is added. After each such fraction has been substantially entirely consumed, insoluble by-product is removed and treatment is continued with the next fraction of refining agent. In this way substantially all of the refining agent is consumed in the first stage treatment.
, Oils of relatively high viscosity are sometimes difcult to refine because the by-product and the oil tend to form a gelatinous mass which prevents complete utilization of the refining agent and makes it diflicult to recover the refined oil. In such cases, I may dilute the oil with a suitable solvent, for instance, a lighter hydrocarbon such as kerosene. point in the refining process, but I prefer to dilute the oil prior to its treatment. The diluent may be removed from the refined oil by disti1lation.
In the following example the term barrel is used to designate a unit of 42 gallons.
Example An acid refined, asphalt base oil was further refined by the process illustrated diagrammatically by the drawing. A quantity of insoluble residue, obtained by filtration of the mixture from a previous single-stage treatment of the same oil, containing 18.7% of metallic sodium, was mixed with untreated oil in the proportion of 82.25 lbs. of residue. per barrel of oil, corresponding to about 7 lbs. of metallic sodium per barrel of oil and the mixture was agitated at 215-225 C. until tests showed that substantially no metallic sodium remained. This required about 12 hours. The mixture was then filtered and the residue, consisting of insoluble polymer and some oil, was discarded. The filtrate, consisting of partially refined oil, was agitated at 215-225 C., for '7l/2 hours with 24.5 lbs. of metallic sodium per barrelv of oil. The insoluble polymer and unreacted sodium were then filtered oiT from the refined oil. The characteristics of the oil before and after treating by the above twostage treatment are shown in the following table. y The characteristics were determined by the standard methods of the American Society for Testing Materials.
Such dilution may be made at any Characteristics Befflrlt'eat' After treatment Neutralization N o 0.00 0.00 oqior N.P.A..No 2 1 85 Color Saybolt +18 ("Prirne whiteu Sligh oxidation No; 14. 1 1. 7 Steam emulsion N o 200 15 Viscosity at F. 1 50 sec 146 sec. Flush point 325 F 330 F. Fire point 365 370 F. 90
The residue from the above two-stage treatment contained 31% of metallic sodium. It was mixed with a fresh quantity of cillin the proportion of '79 lbs. of residue per barrel of oil, cor- 95 responding to about 24.5 lbs. of metallic sodium per barrel of oil. The mixture was agitated at .m5-225 C. for 12 hours and then filtered. The refined oil thus obtained had the following characteristics: 100
Neutralization No 0.00 Color N. P. A. No 1 Color Saybolt +10 Sligh oxidation No 5.5 Steam emulsion No. 59 Viscosity at 100 F 154 sec. Flash point 325 F. Fire point 370 F.
The residue from the filtration, contained13.5% H0 of metallic sodium and was used as treating agent in the first stage of a succeeding two-stage treatment. v
The hydrocarbon to be refined may be previously treated by any known process; for instance, treatment with sulfuric acid, fullers earth, aluminum chloride, or other known refining agent. Such pre-treatment, preceding refining with metallic refining agent is often desirable because it decreases the amount of Ametal consumed.
My invention is not restricted to the use of alkali metal as refining agent, but may be applied to the use of any metallic refining agent which undergoes chemical reaction with the hydrocarbon during the treating process and which l causes the formation of an insoluble by-product.
The invention is also not restricted to any particular means of contacting the hydrocarbon with the-refining agent.
My invention may be used to refine any hydrocarbon material in liquid state, including solutions of hydrocarbons. It is especially adapted for the treatment of petroleum hydrocarbons, regardless of their source or previous treatment.
It may be used for the lighter grades of such hydrocarbons, such as gasoline'and kerosene and is particularly adapted for refining hydrocarbons of relatively-high viscosity, such as lubricating oils.
The chief advantage of my invention is that by it a hydrocarbon material may bev refined to practically any desired degree lwith complete utilization, and therefore without waste, of metallic refining agent. A further advantage is that `it affords a means for using the residues from In the specification and claims, the terms oil and hydrocarbon oil mean a liquid hydrocarbon material having an S. U. V. viscosity of 50 seconds or more at F. For the sake of brevity, the term, reactive metal" is used in the claims to mean a metallic rening agent capable of chemically reacting with the constituents and impurities of the hydrocarbon or hydrocarbon oil treated therewith. Likewise, the term polymer is used in the claims to designate the insoluble treatment by-products formed during the treatment of a liquid hydrocarbon material with reactive metal, as defined above.
I claim:
1. A cyclic process for refining liquid hydrocarbons comprising treating said liquid With alkali metal-polymer mixture at a temperature above the melting point of the alkali metal until substantially complete consumption of said metal is obtained, removing polymer, completing the reining of said liquid by treating with a fresh supply of the alkali metal in large excess, separating refined liquid, utilizing the recovered metalpolymer mixture for complete refinement of an amount of untreated liquid hydrocarbon insufficient to use up the molten alkali metal in said mixture, separating rened liquid, and utilizing the residual metal-polymer mixture and a new batch of liquid to renew the cycle.
2. A process for rening a liquid hydrocarbon comprising agitating a mixture of polymer and alkali metal recovered from a previous rening operation with said hydrocarbon at 10G-275 C. until the metal is substantially entirely consumed,
separating partially refined hydrocarbon from polymer, agitating said partially refined hydrocarbon with a large excess of alkali metal at 10G-275 C. until the desired degree of refinement is obtained, separating a mixture of polymer and unreacted metal from refined hydrocarbon, agitating said separated mixture at 1GO-275 C. with an amount of unrened hydrocarbon insuicient to use up said unreacted metal until the desired degree of refinement is obtained, separating a mixture of polymer and unreacted metal from reined hydrocarbon and using the last said mixture to renne partially a fresh quantity of the hydrocarbon.
3. A process for rening a liquid hydrocarbon comprising agitating a mixtureof polymer and sodium recovered from a previous refining operation with said hydrocarbon at 10D-275 C. until the sodium is substantially entirely consumed, filtering to remove partially refined hydrocarbon from polymer, agitating said partially refined hydrocarbon with a large excess of sodium at 10U-275 C. until the desired degree of renement is obtained, ltering .to remove a mixture of polymer and unreacted metal from rened hydro- 100 carbon, agitating said separated mixture' at 1D0-275" C. with an amount of unrened hydrocarbon insufficient to use up said unreacted metal until the desired degree of refinement is obtained, ltering to remove a mixture of polymer and sodium from rened hydrocarbon andusing the last said mixture to refine partially a fresh quan tity of vthe hydrocarbon.` l
RICHARD SHEPARD VOSl-l.v
soy
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US551166A US1962698A (en) | 1931-07-16 | 1931-07-16 | Refining liquid hydrocarbons |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US551166A US1962698A (en) | 1931-07-16 | 1931-07-16 | Refining liquid hydrocarbons |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1962698A true US1962698A (en) | 1934-06-12 |
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ID=24200126
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US551166A Expired - Lifetime US1962698A (en) | 1931-07-16 | 1931-07-16 | Refining liquid hydrocarbons |
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| Country | Link |
|---|---|
| US (1) | US1962698A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2772211A (en) * | 1953-05-28 | 1956-11-27 | Ethyl Corp | Treatment of hydrocarbon stocks with sodium |
| US2773805A (en) * | 1954-02-01 | 1956-12-11 | Exxon Research Engineering Co | Desulfurization of cracked naphthas with formaldehyde and sodium |
| US2927074A (en) * | 1955-07-07 | 1960-03-01 | Kellogg M W Co | Purification of hydrocarbon oils using sodium |
| US3004912A (en) * | 1959-04-13 | 1961-10-17 | Nat Distillers Chem Corp | Desulfurization process utilizing metallic sodium and recycling of sludge |
-
1931
- 1931-07-16 US US551166A patent/US1962698A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2772211A (en) * | 1953-05-28 | 1956-11-27 | Ethyl Corp | Treatment of hydrocarbon stocks with sodium |
| US2773805A (en) * | 1954-02-01 | 1956-12-11 | Exxon Research Engineering Co | Desulfurization of cracked naphthas with formaldehyde and sodium |
| US2927074A (en) * | 1955-07-07 | 1960-03-01 | Kellogg M W Co | Purification of hydrocarbon oils using sodium |
| US3004912A (en) * | 1959-04-13 | 1961-10-17 | Nat Distillers Chem Corp | Desulfurization process utilizing metallic sodium and recycling of sludge |
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