US3279901A - Distillate fuels - Google Patents
Distillate fuels Download PDFInfo
- Publication number
- US3279901A US3279901A US305859A US30585963A US3279901A US 3279901 A US3279901 A US 3279901A US 305859 A US305859 A US 305859A US 30585963 A US30585963 A US 30585963A US 3279901 A US3279901 A US 3279901A
- Authority
- US
- United States
- Prior art keywords
- water
- alkyl
- carbon atoms
- group
- fuel
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/12—Inorganic compounds
- C10L1/1233—Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof
- C10L1/125—Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/183—Organic compounds containing oxygen containing hydroxy groups; Salts thereof at least one hydroxy group bound to an aromatic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/1881—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
- C10L1/2225—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates hydroxy containing
Definitions
- the additive mixture consists of three ingredients in relative amounts of from 1 to 9 parts by weight of a fatty acid, from 1 to parts by weight of an amine selected from the group consisting of an alkyl polyamine, an alkanol amine, and preferably a mixture of alkanol amines, and from 1 to 8 parts by weight of an alkyl phenol.
- the fatty acids suitable for this invention include those having from 16 to 20 carbon atoms.
- the acid may be saturated, for example, palmitic or s-tearic acid or it may be unsaturated.
- the preferred acids are those which contain '1 (oleic), 2 (linoleic), or 3 (linolenic) double bonds.
- Other suitable acids include palmitoleic, elaidic, eleostearic, licanic, ricinoleic, vaccenic, and punicic. These acids may be substituted or unsubstituted, however, it is preferred that they be unsubstituted.
- the amines that are effective are alkyl polyarnines having from 1 to 3 carbons per amine group.
- Alkyl diamines such as ethylene diamine are preferred.
- Suitable amino alcohols include primary, secondary and tertiary alkyl amino alcohols containing from 2 to 5 carbon atoms per alkyl group.
- the preferred amino alcohols are the primary, secondary and tertiary isopropanol 3,279,901 Patented Oct. 18, 1966 amines, to wit, monoisopropanol amine, d-iisopr-opanol amine, and triisopropanol amine. Economically, mixtures of isopropanol amines are preferred.
- the alkyl phenols for this invention include the monoand polyhydroxy compounds having an alkyl group containing from 8 to 12 carbon atoms.
- the alkyl group saturated or unsaturated, can be branched or straight chained.
- the group may be substituted with halogen groups or the like but is preferably unsubstituted.
- the aryl group, phenyl or naphthyl may be substituted with a halogen or the like, but it is preferably unsubstituted.
- the presence of other alkyl groups on the aryl group will not hinder the performance of a phenol so long as the phenol has at least one alkyl group containing from 8 through 12 carbon atoms.
- the cresols that is, the methylphenols
- the oils in which the additive mixture of this invention may be incorporated are liquid petroleum distillate products boiling in a range between about 75 and about 900 F.
- Such products include gasolines, aviation turbo jet fuels, kerosenes, diesel fuels, transformer oils, turbine oils and heating oils.
- the additives are particularly useful in distillate fuels boiling in a range between about 250 F. and about 750 F.
- Such fuels include turbo jet engine fuels, diesel fuels and heating oils.
- the amount of the additive mixture needed to form the microemulsion will depend upon a variety of factors, for
- the particular additive mixture employed typeof fuel, and the amount of water in the fuel.
- the addition of a small amount of the additive mixture to the distillate equal to from 10% vby weight to 200% the amount of the water in the fuel will form a microernulsion with the water.
- microemulsifyi-ng additive mixture may, in accordance with this invention, be employed in conjunction with a variety of other additives commonly used in fuels.
- Typical additives are rust inhibitors, corrosion inhibitors, antioxidants, dispersants, dyes, dye stabilizers, antistatic agents, and the like. it may be found to be convenient to prepare additive concentr-tae for use in the various types of fuels and thus add all of the additives simultaneous y.
- a fuel oil which is subject to contamination by Water and which is inhibited against formation of large ice crystals which can cause valve and filter plugging, containing: a minor amount of a water microemulsifying addit-ive mixture, sufficient to microemulsify water contamination into said oil, of about 1 to 9 par-ts by weight of C to C fatty acid, about 1 to 8 parts of alkyl phenol wherein said alkyl group has 8 to 12 carbon atoms, and about 1 to 5 parts by weight of an amine selected from the group consisting of alkyl polyamine having 1 to 3 carbon atoms per amine 'group and an alkyl amino alcohol containing 2 to 5 carbon atoms per alkyl group.
- a fuel oil according to claim 1 wherein said minor amount of additive mixture is equal to from 10% to 200% the amount of water in the distillate.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
United States Patent 3,279,901 DISTILLATE FUELS Max L. Robbins, South Orange, and Darrell W. Brownawell, Scotch Plains, N.J., assignors to Esso Research and Engineering Company, a corporation of Delaware No Drawing. Filed Aug. 30, 1963, Ser. No. 305,859 3 Claims. (Cl. 44-66) This invention concerns an improved petroleum distillate composition and, more particularly, relates to a distillate containing additives which obviate the problems caused by water being entrained in the distillate.
Water normally enters an outdoor fuel tank when the ambient temperature rises. At this time the fuel tank walls are colder than the air; therefore water vapor precipitates and freezes onto the tank walls. When the fuel tank walls warm sufficiently, the ice melts and admixes with the fuel. This entrained water causes many problems; for example, ice formation is a common cause of burner failure in home heating oil installations, where the fuel is stored -outside.- The water in the fuel oil is often dispersed in large droplets. These droplets on freezing form large spherical ice crystals which tend to plug the valve and line leading to the burner. At temperatures where wax has precipitated from the fuel, ice crystals aggravate wax plugging of the valve and line. In addition to the problem of ice formation, water ad heres to impurities in a fuel causing a sticky sludge. This, of course, increases the tfilter plugging tendencies of the fuel oil.
It has now been discovered that the severity of the problem caused by entrained Water can be greatly reduced and in many instances the problem virtually eliminated by employing a particular mixture of additives. The periodic addition of the additives of this invention to -a stored fuel oil causes the formation of a microemulsion. This microemulsion will keep the water fiom settling and collecting on the bottom of the tank. Since the water is microemulsified, on freezing only very small ice crystals will form. These small crystals will not plug the valve or line and will be pumped through the burner where the water will eventually be eliminated. In addition, the additive mixture of this invention separates water that adheres to the sludge, thus breaking up the sludge.
The additive mixture consists of three ingredients in relative amounts of from 1 to 9 parts by weight of a fatty acid, from 1 to parts by weight of an amine selected from the group consisting of an alkyl polyamine, an alkanol amine, and preferably a mixture of alkanol amines, and from 1 to 8 parts by weight of an alkyl phenol.
The fatty acids suitable for this invention include those having from 16 to 20 carbon atoms. The acid may be saturated, for example, palmitic or s-tearic acid or it may be unsaturated. The preferred acids are those which contain '1 (oleic), 2 (linoleic), or 3 (linolenic) double bonds. Other suitable acids include palmitoleic, elaidic, eleostearic, licanic, ricinoleic, vaccenic, and punicic. These acids may be substituted or unsubstituted, however, it is preferred that they be unsubstituted.
The amines that are effective are alkyl polyarnines having from 1 to 3 carbons per amine group. Alkyl diamines such as ethylene diamine are preferred.
Although the above-described alkyl amines are effective in the additive mixture of this invention, it has been discovered that certain amino alcohols and preferably mixtures of these amino alcohols are even more effective. Suitable amino alcohols include primary, secondary and tertiary alkyl amino alcohols containing from 2 to 5 carbon atoms per alkyl group. The preferred amino alcohols are the primary, secondary and tertiary isopropanol 3,279,901 Patented Oct. 18, 1966 amines, to wit, monoisopropanol amine, d-iisopr-opanol amine, and triisopropanol amine. Economically, mixtures of isopropanol amines are preferred.
The alkyl phenols for this invention include the monoand polyhydroxy compounds having an alkyl group containing from 8 to 12 carbon atoms. The alkyl group, saturated or unsaturated, can be branched or straight chained. The group may be substituted with halogen groups or the like but is preferably unsubstituted. Likewise, the aryl group, phenyl or naphthyl, may be substituted with a halogen or the like, but it is preferably unsubstituted. The presence of other alkyl groups on the aryl group will not hinder the performance of a phenol so long as the phenol has at least one alkyl group containing from 8 through 12 carbon atoms. Thus it is seen that the cresols, that is, the methylphenols, may be used to synthesize the alkyl phenols of this invention.
The oils in which the additive mixture of this invention may be incorporated are liquid petroleum distillate products boiling in a range between about 75 and about 900 F. Such products include gasolines, aviation turbo jet fuels, kerosenes, diesel fuels, transformer oils, turbine oils and heating oils. The additives are particularly useful in distillate fuels boiling in a range between about 250 F. and about 750 F. Such fuels include turbo jet engine fuels, diesel fuels and heating oils.
The amount of the additive mixture needed to form the microemulsion will depend upon a variety of factors, for
example, the particular additive mixture employed, typeof fuel, and the amount of water in the fuel. In general, however, the addition of a small amount of the additive mixture to the distillate equal to from 10% vby weight to 200% the amount of the water in the fuel will form a microernulsion with the water.
The microemulsifyi-ng additive mixture may, in accordance with this invention, be employed in conjunction with a variety of other additives commonly used in fuels. Typical additives are rust inhibitors, corrosion inhibitors, antioxidants, dispersants, dyes, dye stabilizers, antistatic agents, and the like. it may be found to be convenient to prepare additive concentr-tae for use in the various types of fuels and thus add all of the additives simultaneous y.
In order to demonstrate the efiicacy of the additive mixture, tests were performed with a fuel having the following inspection:
Gravity, API 60 F.) 30.5 Color, Tag-Robinson 12 Pensky-Martens flash, 415 (Clevelandopen cup) Sulfur, wt. percent 0.2 Neutralization No. 0.05 Aniline point, F. ASTM distillation, 10 mm. Hg:
Initial boiling point, F. 318 10% point, F. as 432 50% point, F. 508 point, F. 573 Final boiling point, F. 596 Conradson carbon residue percent 0.04
above-identified fuel. In a series of tests utilizing various weight ratios of the ingredients of the additive mixture the fuel was titrated to .the first water haze to determine the amount of water the system would take up as a microemulsion. The results appear in Table I.
TABLE I.-SURFAOTANT MIXTURE RATIO Tall Oil Mixed Fatty Isopro- N onyl Water, Solution Acid panol Phenol g.
Amine 1 1 1 40. 3 Clear. 2 1 2 22. Do. 2 1 1. 3 Do. 5 2 5 13. 6 Do. 3 1 1 42. 5 Do. 5 1 1 13. 7 Slight haze. 1 2 5 3. 9 D0. 1 1 5 2. 1 Do. 1 5 1 0 Initial haze. 5 1 5 0. 6 Clear.
In the absence of the additive mixture a haze appeared as soon as water was added to the system. However, as is seen from the data appearing in Table I, the additive mixture of this invention was effective in causing a substantial amount of water to be microemulsified in the fuel.
What is claimed is:
1. A fuel oil, which is subject to contamination by Water and which is inhibited against formation of large ice crystals which can cause valve and filter plugging, containing: a minor amount of a water microemulsifying addit-ive mixture, sufficient to microemulsify water contamination into said oil, of about 1 to 9 par-ts by weight of C to C fatty acid, about 1 to 8 parts of alkyl phenol wherein said alkyl group has 8 to 12 carbon atoms, and about 1 to 5 parts by weight of an amine selected from the group consisting of alkyl polyamine having 1 to 3 carbon atoms per amine 'group and an alkyl amino alcohol containing 2 to 5 carbon atoms per alkyl group.
2. A fuel oil according to claim 1 wherein said minor amount of additive mixture is equal to from 10% to 200% the amount of water in the distillate.
3. A fuel oil according to claim 1, wherein said alkyl phenol is nonyl phenol, and said amine is a mixture of isopropanol amines.
References Cited by the Examiner UNITED STATES PATENTS 1,976,886 10/1934 Lier 252-357 2,154,850. 4/1939 K-aufrnann 252356 2,247,106 6/ 1941 Vanderbilt 252-308 2,329,251 9/ 1943 Chen-icek 4466 2,550,981 5/1951 Eberz 4460 3,031,278 4/ 1962 Buckmann 44-6 6 DANIEL E. WYMAN, Primary Examiner.
W. H. CA NNON, Assistant Examiner.
Claims (1)
1. A FUEL OIL, WHICH IS SUBJECT TO CONTAMINATION BY WATER AND WHICH IS INHIBITED AGAINST FORMATION OF LARGE ICE CRYSTALS WHICH CAN CAUSE VALVE AND FILTER PLUGGING, CONTAINING: A MINOR AMOUNT OF A WATER MICROEMULSIFYING ADDITIVE MIXTURE, SUFFICIENT TO MICROEMULSIFY WATER CONTAMINATION INTO SAID OIL, OF ABOUT 1 TO 9 PARTS BY WEIGHT OF C16 C20 FATTY ACID, ABOUT 1 TO 8 PARTS OF ALKYL PHENOL WHEREIN SAID ALKYL GROUP HAS 9 TO 12 CARBON ATOMS, AND ABOUT 1 TO 5 PARTS BY WEIGHT OF AN AMINE SELECTED FROM THE GROUP CONSISTING OF ALKYL POLYAMINE HAVING 1 TO 3 CARBON ATOMS PER AMINE GROUP AND AN ALKYL AMINO ALCOHOL CONTAINING 2 TO 5 CARBON ATOMS PER ALKYL GROUP.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US305859A US3279901A (en) | 1963-08-30 | 1963-08-30 | Distillate fuels |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US305859A US3279901A (en) | 1963-08-30 | 1963-08-30 | Distillate fuels |
Publications (1)
Publication Number | Publication Date |
---|---|
US3279901A true US3279901A (en) | 1966-10-18 |
Family
ID=23182673
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US305859A Expired - Lifetime US3279901A (en) | 1963-08-30 | 1963-08-30 | Distillate fuels |
Country Status (1)
Country | Link |
---|---|
US (1) | US3279901A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3527581A (en) * | 1966-10-17 | 1970-09-08 | Exxon Research Engineering Co | Microemulsions of water in hydrocarbon fuel for engines |
US5968211A (en) * | 1995-12-22 | 1999-10-19 | Exxon Research And Engineering Co. | Gasoline additive concentrate |
US6277158B1 (en) | 1996-09-12 | 2001-08-21 | Exxon Research And Engineering Company | Additive concentrate for fuel compositions |
EP2343353A3 (en) * | 2006-01-20 | 2011-11-30 | Palox Limited | Uses of emulsifying agents in non-aqueous fuels and oils |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1976886A (en) * | 1926-10-29 | 1934-10-16 | Firm Chemical Works Formerly S | Preparation of wetting agents for use in alkalizing lyes |
US2154850A (en) * | 1937-09-03 | 1939-04-18 | Tide Water Associated Oil Comp | Insecticide |
US2247106A (en) * | 1937-08-13 | 1941-06-24 | Purdue Research Foundation | Fatty acid salts of polyhydroxy amines |
US2329251A (en) * | 1941-01-21 | 1943-09-14 | Universal Oil Prod Co | Treatment of gasoline |
US2550981A (en) * | 1947-07-12 | 1951-05-01 | Petrolite Corp | Method of inhibiting fogs in hydrocarbon products |
US3031278A (en) * | 1958-01-20 | 1962-04-24 | Union Oil Co | Detergent internal combustion engine fuel |
-
1963
- 1963-08-30 US US305859A patent/US3279901A/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1976886A (en) * | 1926-10-29 | 1934-10-16 | Firm Chemical Works Formerly S | Preparation of wetting agents for use in alkalizing lyes |
US2247106A (en) * | 1937-08-13 | 1941-06-24 | Purdue Research Foundation | Fatty acid salts of polyhydroxy amines |
US2154850A (en) * | 1937-09-03 | 1939-04-18 | Tide Water Associated Oil Comp | Insecticide |
US2329251A (en) * | 1941-01-21 | 1943-09-14 | Universal Oil Prod Co | Treatment of gasoline |
US2550981A (en) * | 1947-07-12 | 1951-05-01 | Petrolite Corp | Method of inhibiting fogs in hydrocarbon products |
US3031278A (en) * | 1958-01-20 | 1962-04-24 | Union Oil Co | Detergent internal combustion engine fuel |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3527581A (en) * | 1966-10-17 | 1970-09-08 | Exxon Research Engineering Co | Microemulsions of water in hydrocarbon fuel for engines |
US5968211A (en) * | 1995-12-22 | 1999-10-19 | Exxon Research And Engineering Co. | Gasoline additive concentrate |
US6277158B1 (en) | 1996-09-12 | 2001-08-21 | Exxon Research And Engineering Company | Additive concentrate for fuel compositions |
EP2343353A3 (en) * | 2006-01-20 | 2011-11-30 | Palox Limited | Uses of emulsifying agents in non-aqueous fuels and oils |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2684292A (en) | Fuel oil composition | |
US2553183A (en) | Fuel oil composition | |
US3930810A (en) | Additives for petroleum distillates | |
US2575003A (en) | Fuel oil composition | |
US2736641A (en) | Fuel oil additive | |
US3251664A (en) | Fuel compositions containing branched polyalkylenepolyamines and derivatives thereof | |
US2726942A (en) | Motor fuels | |
US3063819A (en) | Fuel composition | |
US2883277A (en) | Synergistic corrosion inhibiting composition for gasoline | |
US3279901A (en) | Distillate fuels | |
US2632694A (en) | Petroleum distillates containing ammonium mahogany sulfonates and oil soluble carboxylic acids to prevent corrosion | |
US3088815A (en) | Fuel oil | |
US2935389A (en) | Rust inhibited mineral oil compositions | |
US3674450A (en) | Antistatic additive for hydrocarbon fuels | |
US3309181A (en) | Transesterification product | |
US2959915A (en) | Fuel for and method of operating a jet engine | |
US2857333A (en) | Corrosion inhibitors | |
US3150147A (en) | Imidazoline salt of citrimic acid as corrosion inhibitor for hydrocarbon fuel | |
US2791495A (en) | Rust inhibited distillate products | |
US2966458A (en) | Corrosion inhibition and corrosion inhibited hydrocarbon | |
US3056666A (en) | Hydrocarbon fuels stabilized against sediment | |
US3929655A (en) | Additives for hydrocarbonaceous materials | |
US3018173A (en) | Stabilization of hydrocarbons | |
US2961309A (en) | Gasoline composition | |
US3240574A (en) | Stabilization of organic compounds |