US2247927A - Treatment of hydrocarbons - Google Patents
Treatment of hydrocarbons Download PDFInfo
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- US2247927A US2247927A US195361A US19536138A US2247927A US 2247927 A US2247927 A US 2247927A US 195361 A US195361 A US 195361A US 19536138 A US19536138 A US 19536138A US 2247927 A US2247927 A US 2247927A
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- US
- United States
- Prior art keywords
- impurities
- removal
- agent
- compounds
- color
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 150000002430 hydrocarbons Chemical class 0.000 title description 22
- 229930195733 hydrocarbon Natural products 0.000 title description 12
- 239000012535 impurity Substances 0.000 description 31
- 239000003795 chemical substances by application Substances 0.000 description 28
- 239000000203 mixture Substances 0.000 description 17
- 239000000446 fuel Substances 0.000 description 14
- 230000002401 inhibitory effect Effects 0.000 description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 10
- 239000010687 lubricating oil Substances 0.000 description 10
- 239000003208 petroleum Substances 0.000 description 10
- 239000005864 Sulphur Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- 235000011149 sulphuric acid Nutrition 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 239000001117 sulphuric acid Substances 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000010802 sludge Substances 0.000 description 7
- -1 aluminum chloride Chemical class 0.000 description 6
- 230000002378 acidificating effect Effects 0.000 description 5
- 238000002485 combustion reaction Methods 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 3
- OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- PCAXITAPTVOLGL-UHFFFAOYSA-N 2,3-diaminophenol Chemical compound NC1=CC=CC(O)=C1N PCAXITAPTVOLGL-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- TWBPWBPGNQWFSJ-UHFFFAOYSA-N 2-phenylaniline Chemical group NC1=CC=CC=C1C1=CC=CC=C1 TWBPWBPGNQWFSJ-UHFFFAOYSA-N 0.000 description 1
- QPQKUYVSJWQSDY-UHFFFAOYSA-N 4-phenyldiazenylaniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=CC=C1 QPQKUYVSJWQSDY-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical group CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- PONXTPCRRASWKW-KBPBESRZSA-N diphenylethylenediamine Chemical compound C1([C@H](N)[C@@H](N)C=2C=CC=CC=2)=CC=CC=C1 PONXTPCRRASWKW-KBPBESRZSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- ALIFPGGMJDWMJH-UHFFFAOYSA-N n-phenyldiazenylaniline Chemical compound C=1C=CC=CC=1NN=NC1=CC=CC=C1 ALIFPGGMJDWMJH-UHFFFAOYSA-N 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000005120 petroleum cracking Methods 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 229940067157 phenylhydrazine Drugs 0.000 description 1
- BDJXVNRFAQSMAA-UHFFFAOYSA-N quinhydrone Chemical compound OC1=CC=C(O)C=C1.O=C1C=CC(=O)C=C1 BDJXVNRFAQSMAA-UHFFFAOYSA-N 0.000 description 1
- 229940052881 quinhydrone Drugs 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G17/00—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge
- C10G17/02—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge with acids or acid-containing liquids, e.g. acid sludge
- C10G17/04—Liquid-liquid treatment forming two immiscible phases
- C10G17/06—Liquid-liquid treatment forming two immiscible phases using acids derived from sulfur or acid sludge thereof
Definitions
- This invention relates to the treatment of hydrocarbon compounds and mixtures thereof, including motor and heating plant fuels and lubricating oils, to improve them as-to color, composition', properties and characteristics, and more particularly to their treatment for the purpose of removing objectionable impurities therefrom for rendering them more stable in composition and color, and, when the hydrocarbon compounds are lubricating oils, for also reducing the tendency of the oil to sludge or decompose underoperating conditions such as in the crank case of an internal combustion engine.
- sulphur compounds from hydrocarbon compounds and mixtures thereof, including both motor and heating fuels and lubricating oils,
- hydrocarbon compounds may be unsaturated, by various acidic treating agents such as the mineral acids.
- Sulphuric acid is the mineral acid or acidic treating agent most commonly used for this purpose, but anhydrous metallic halides, such as aluminum chloride, are acidic treating agents which have alsobeen used for this purpose.
- these polymerized hydrocarbons have a higher boiling or vaporizing point than is desirable in an internal combustion engine fuel, and therefore are sometimes removed from the desulphurized or treated mixture and discarded, which decreases the yield of marketablefuel obtained from a given quantity of untreated hydrocarbon compounds.
- the polymerization of unpurities removed greatly increased/if the removal action is carried on in the presence of an accelcrating or inhibiting agent or substance.
- uct is obtained, and the impurities removal processes may be performed at higher temperatures not heretofore feasible or desirable.
- Various organic compounds have been found suitable as the accelerating or inhibiting agent, and may be used in the usual methods of removing impurities from hydrocarbon compounds.
- the selection of the accelerating or inhibiting agent depends somewhat upon the exact nature of the impurities to be removed, the degrees of jun satur ation of th hydrocarbon compounds from whichthe-impurities are tobe removed, the
- the amount of the inhibiting agent which it is desirable to use, while varying somewhat with the material to be treated, the impurities to be removed, and the character of the impurities removal agent, is in general less than the molal quantity of the impurities removal agent employed;
- the hydrocarbon compounds to be treated are viscous products
- their treatment maybe facilitated by first reducing their viscosity, either by heating the same first to reduce the viscosity or by mixing therewith the necessary amount of a thin liquid such as, for example, gasoline, which viscosity reducing addition agent, such as gasoline, can be removed readily by volatilization cording to my discovery, a more desirable prodties.
- the inhibiting agent may be added either to the impurities removal agent before the latter is added to the hydrocarbon mixtures, or to the hydrocarbon mixture before the impurities removal agent is added to the hydrocarbon mixture. I prefer to add the inhibiting agent to the hydrocarbon mixture first, and then add the impurities removal agent to this combined mixture, and the improved method of treatment may be of either the continuous or batch type.
- reaction I may be agitated continuously until the reaction is complete.
- the reaction I has found is usually completed within about ten minutes when the acid treatment is used for the removal of sulphur, and within approximately one half hour if a metallic halide is used as the removal agent. After the reaction is complete,
- the combined mixture is left quiescent, whereupon the residue separates out carrying the impurities and the treating agent, which then may it for the market and to remove any viscosity reducing agent.
- the residue may be then disposed of as usual in the industry, or treated for the recovery of any valuable components thereof.
- the acidic impurities removal treatment often required several hours or days in order to geta high percentage of removal of the" impuri-
- the use of the inhibiting agent also speeds up the reaction and makes the removal of "impurities more complete, without undesirable polymerization or alteration of the hydrocarbons. I have found that by the use of the inhibiting agent, the action is more rapid'at the same temperatures, and one may use higher temperatures during the removal reaction in order to speed up the reaction without materially increasing the polymerization of the unsaturated compounds, which polymerization oralteration always heretofore occurred to a very great extent whenever the impurities removal reaction was speeded up by the use of the higher temperatures.
- Removal-of impurities with such an inhibiting agent may be applied to hydrocarbon mixtures in any stage of refinement or in crude form,-and
- the amount of acidic treating agent can be increased to the desired point, impractical otherwise, in order to secure desired refining results.
- quantities of 98% sulphuric acid as 30 pounds per barrel or more can be used successfully and to advantage Without excessive loss of the lubricating material itself.
- lubricating oils intended for use in automotive engine lubrication can be given still greater color stability and resistance to sludging by the admixture with the oil of the desired, and prefercases, but usually a'larger percentage of the quinhydrone is preferred up to a percentage which is soluble in the oil.
- the method of treating petroleum lubricating oils and petroleum motor and heating fuels normally having color instability, a tendency to gum formation and impurities such as sulphur, to stabilize their color, reduce their tendency to gum and sludge formation, to accelerate, and increase the percentage of the removal of some objectionable impurities, and to inhibit polymerization of unsaturated compounds which comprises treating such oils and fuels in the liquid phase at the same time with sulphuric acid and a cyclic amine, in which the amount of the added amine is in general less than approximately the molal quantity of the sulphuric acid which is added.
- the method of treating petroleum lubricating oils and petroleum motor and heating fuels normally having color instability, a tendency to gum formation and impurities such as sulphur, to stabilize their color, reduce their tendency to gum and sludge formation, to accelerate, and increase the percentage of the removal of some objectionable impurities, and to inhibit polymerization of unsaturated compounds which comprises treating such oils and fuels in the liquid phase at the same time with a mineral'acid and a cyclic amine, to which the amine is added to said oils and fuels at least as early as said acid.
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)
- Lubricants (AREA)
Description
Patented July 1, 1941 UNITED STATES No Drawing. Application March 11, 1938,
7 Serial No. 195,361
S'Claims. (01. 196-31) This inventionrelates to the treatment of hydrocarbon compounds and mixtures thereof, including motor and heating plant fuels and lubricating oils, to improve them as-to color, composition', properties and characteristics, and more particularly to their treatment for the purpose of removing objectionable impurities therefrom for rendering them more stable in composition and color, and, when the hydrocarbon compounds are lubricating oils, for also reducing the tendency of the oil to sludge or decompose underoperating conditions such as in the crank case of an internal combustion engine. Among examples of the impurities which may be readily removed or rendered ,unobjectionable by this invention may be mentioned sulphur, whether in a combined or uncombined condition, gums and gum forming compounds, and unstable hydrocarbon constituen ts.,, Heretofore ithas been common practice to partially remove some undesirable impurities,
including sulphur compounds, from hydrocarbon compounds and mixtures thereof, including both motor and heating fuels and lubricating oils,
some of which hydrocarbon compounds may be unsaturated, by various acidic treating agents such as the mineral acids. Sulphuric acid is the mineral acid or acidic treating agent most commonly used for this purpose, but anhydrous metallic halides, such as aluminum chloride, are acidic treating agents which have alsobeen used for this purpose. v
In the usual refining treatment of certain hydrocarbon mixtures, such, for example, as petroleum compounds and particularly the distillates from petroleum cracking stills, it has been found that the unsaturated hydrocarbons in those mixtures or distillates, that is, hydrocarbons containing less than the maximum amount of hydrogen whichcould be included in the combination,,are,
,to a considerable extent, polymerized into undesirable hydrocarbon compounds, many of which are resinous in character, by the impurities removal agents heretofore employed. Such undesirable compounds when burned in an internal combustion engine are more likely to knock or detonate than are the unsaturated compounds before their polymerization.
Frequently these polymerized hydrocarbons have a higher boiling or vaporizing point than is desirable in an internal combustion engine fuel, and therefore are sometimes removed from the desulphurized or treated mixture and discarded, which decreases the yield of marketablefuel obtained from a given quantity of untreated hydrocarbon compounds. The polymerization of unpurities removed greatly increased/if the removal action is carried on in the presence of an accelcrating or inhibiting agent or substance.
uct is obtained, and the impurities removal processes may be performed at higher temperatures not heretofore feasible or desirable. Various organic compounds have been found suitable as the accelerating or inhibiting agent, and may be used in the usual methods of removing impurities from hydrocarbon compounds.
The selection of the accelerating or inhibiting agent depends somewhat upon the exact nature of the impurities to be removed, the degrees of jun satur ation of th hydrocarbon compounds from whichthe-impurities are tobe removed, the
amount of impuritiesto be removed, and the conditions under which the removal is to be performed. Ingeneral, I have found that anhydrous treating agents yield better results than those in which 'water dilution occurs, and when sulphuric acid is used, I have found that in the presenceof an inhibiting agent, a concentrated sulphuric acid as near as possible to a one hundred percent pure acid yields more satisfactory results than does commercial oil of vitriol acid, which is usually about ninety-five. percent strength.
The amount of the inhibiting agent which it is desirable to use, while varying somewhat with the material to be treated, the impurities to be removed, and the character of the impurities removal agent, is in general less than the molal quantity of the impurities removal agent employed; I
When the hydrocarbon compounds to be treated are viscous products, their treatment maybe facilitated by first reducing their viscosity, either by heating the same first to reduce the viscosity or by mixing therewith the necessary amount of a thin liquid such as, for example, gasoline, which viscosity reducing addition agent, such as gasoline, can be removed readily by volatilization cording to my discovery, a more desirable prodties.
-methylaniline, m-phenylenediamine, p-phenylenediamine, 2.4 diaminophenol, o-aminodiphenyl, methyl-or ethyl-aniline, dimethyl or diethyl aniline, m-toluylenediamine, diphenylethylenediamine, phenylhydrazine, diphenylamine, ben'zidine, aminoazobenzene, and diazoaminobenzene.
The inhibiting agent may be added either to the impurities removal agent before the latter is added to the hydrocarbon mixtures, or to the hydrocarbon mixture before the impurities removal agent is added to the hydrocarbon mixture. I prefer to add the inhibiting agent to the hydrocarbon mixture first, and then add the impurities removal agent to this combined mixture, and the improved method of treatment may be of either the continuous or batch type.
After the hydrocarbon compounds or mixtures thereof have been treated with the impurities removal agent and the inhibiting agent, the
complete mixture may be agitated continuously until the reaction is complete. The reaction I have found is usually completed within about ten minutes when the acid treatment is used for the removal of sulphur, and within approximately one half hour if a metallic halide is used as the removal agent. After the reaction is complete,
'the combined mixture is left quiescent, whereupon the residue separates out carrying the impurities and the treating agent, which then may it for the market and to remove any viscosity reducing agent. The residue may be then disposed of as usual in the industry, or treated for the recovery of any valuable components thereof.
Without the use of the inhibiting agent or material, the acidic impurities removal treatment often required several hours or days in order to geta high percentage of removal of the" impuri- The use of the inhibiting agent also speeds up the reaction and makes the removal of "impurities more complete, without undesirable polymerization or alteration of the hydrocarbons. I have found that by the use of the inhibiting agent, the action is more rapid'at the same temperatures, and one may use higher temperatures during the removal reaction in order to speed up the reaction without materially increasing the polymerization of the unsaturated compounds, which polymerization oralteration always heretofore occurred to a very great extent whenever the impurities removal reaction was speeded up by the use of the higher temperatures.
Removal-of impurities with such an inhibiting agent may be applied to hydrocarbon mixtures in any stage of refinement or in crude form,-and
produces a product which I have found will stand exposure to light more satisfactorilythan' products obtained by similar removal processes without the use of the inhibitor. The removal of sulphur, for example, when accomplished-in the presence of the inhibitor, is more complete for a given amount of the sulphur removing agent than is possible without the use of an inhibitor,
and the inhibitor may be used without any change in the apparatus used heretofore for sulphur removal. The amount of acidic treating agent can be increased to the desired point, impractical otherwise, in order to secure desired refining results. For example, in treating Pennsylvania lubricating oils, such quantities of 98% sulphuric acid as 30 pounds per barrel or more can be used successfully and to advantage Without excessive loss of the lubricating material itself.
When motor fuels, such as gasolines, are treated in accordance with this invention, the resulting product is non-corrosive, lower in gum content, very much more stable as evidenced by the distillation test residues which are relatively light colored, and has better color and color stability. When heavier petroleum products such as lubricating oils are treated in accordance with this invention, the color, non-corrosiveness, tendency to sludge or decompose under operating conditions, particularly under the conditions existing in the crank'cases of internal combustion engines, and the resistance to heat are improved in a similar manner. I have also discovered that lubricating oils intended for use in automotive engine lubrication can be given still greater color stability and resistance to sludging by the admixture with the oil of the desired, and prefercases, but usually a'larger percentage of the quinhydrone is preferred up to a percentage which is soluble in the oil.
In the foregoing description, reference has been made to sulphur-as one of the impurities that may be removed or rendered unobjectionable in accordance with this invention, but it will be understood that the exact composition of the impurities which are found in petroleum hydrocarbons is not definitely known, but sulphur is one of the major impurities found in such petroleum products which can be removed or rendered unobjectionableby this invention. It is also believed that the removal of undesirable nitrogen compounds'is facilitated by this invention.
This application is a continuation in part of my prior and copending application Serial No.
431,990, filed February 27, 1930.
Iclaim as my invention:
1. The-"method of removing impurities from petroleum lubricating oils and motor and petroleum heating fuels, and increasing their color stability and reducing their tendency to'gum and sludge formation, which comprises treating such' oi-ls and fuels at the same timewith concentrated sulphuric acid andan aryl amine.
2. The method of treating petroleum lubricating oils and petroleum motor and heating fuels normally having color instability, a tendency to gum formation and impurities such as sulphur, to stabilize their color; reduce their tendency to gum and sludge formation, to accelerate, and increase the percentage of the removal of some objectionable impurities, and to inhibit polymerization of unsaturated compounds which comprises treating such oils and fuels in the liquid phase at the same time with a mineral acid and a cyclic to stabilize their color, reduce their tendency to gum and sludge formation, to accelerate, and increase the percentage of the removal of some objectionable impurities, and to inhibit polymerization of unsaturated compounds which comprises treating such oils and fuels in the liquid phase at the same time with sulphuric acid and a cyclic amine.
4. The method of treating petroleum lubricating oils and petroleum motor and heating fuels normally having color instability, a tendency to gum formation and impurities such as sulphur, to stabilize their color, reduce their tendency to gum and sludge formation, to accelerate, and increase the percentage of the removal of some objectionable impurities, and to inhibit polymerization of unsaturated compounds which comprises treating such oils and fuels in the liquid phase at the same time with sulphuric acid and a cyclic amine, in which the amount of the added amine is in general less than approximately the molal quantity of the sulphuric acid which is added.
5. The method of treating petroleum lubricating oils and petroleum motor and heating fuels normally having color instability, a tendency to gum formation and impurities such as sulphur, to stabilize their color, reduce their tendency to gum and sludge formation, to accelerate, and increase the percentage of the removal of some objectionable impurities, and to inhibit polymerization of unsaturated compounds which comprises treating such oils and fuels in the liquid phase at the same time with a mineral'acid and a cyclic amine, to which the amine is added to said oils and fuels at least as early as said acid.
WILLIAM ALVAH SMITH.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US195361A US2247927A (en) | 1938-03-11 | 1938-03-11 | Treatment of hydrocarbons |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US195361A US2247927A (en) | 1938-03-11 | 1938-03-11 | Treatment of hydrocarbons |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2247927A true US2247927A (en) | 1941-07-01 |
Family
ID=22721130
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US195361A Expired - Lifetime US2247927A (en) | 1938-03-11 | 1938-03-11 | Treatment of hydrocarbons |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2247927A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2462829A (en) * | 1946-05-28 | 1949-02-22 | Griffin Chemical Company | Preparation of oil soluble petroleum sulfonates |
| US2570269A (en) * | 1948-03-25 | 1951-10-09 | Pittsburgh Plate Glass Co | Stabillation of copolymerizable polyester-monomer mixture by means of a salt of a substituted hydrazine |
| US3113433A (en) * | 1962-03-07 | 1963-12-10 | Kohlman John William | Brake system |
| US3265614A (en) * | 1964-01-13 | 1966-08-09 | Petrolite Corp | Removal of sulfur bodies |
| US3309413A (en) * | 1963-03-04 | 1967-03-14 | Howe Baker Eng | Aromatic desulfurization |
| US4201662A (en) * | 1979-04-03 | 1980-05-06 | Phillips Petroleum Company | Process for converting sulfur in hydrocarbon to water soluble form |
-
1938
- 1938-03-11 US US195361A patent/US2247927A/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2462829A (en) * | 1946-05-28 | 1949-02-22 | Griffin Chemical Company | Preparation of oil soluble petroleum sulfonates |
| US2570269A (en) * | 1948-03-25 | 1951-10-09 | Pittsburgh Plate Glass Co | Stabillation of copolymerizable polyester-monomer mixture by means of a salt of a substituted hydrazine |
| US3113433A (en) * | 1962-03-07 | 1963-12-10 | Kohlman John William | Brake system |
| US3309413A (en) * | 1963-03-04 | 1967-03-14 | Howe Baker Eng | Aromatic desulfurization |
| US3265614A (en) * | 1964-01-13 | 1966-08-09 | Petrolite Corp | Removal of sulfur bodies |
| US4201662A (en) * | 1979-04-03 | 1980-05-06 | Phillips Petroleum Company | Process for converting sulfur in hydrocarbon to water soluble form |
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