US2481859A - Diesel fuel - Google Patents

Diesel fuel Download PDF

Info

Publication number
US2481859A
US2481859A US694438A US69443846A US2481859A US 2481859 A US2481859 A US 2481859A US 694438 A US694438 A US 694438A US 69443846 A US69443846 A US 69443846A US 2481859 A US2481859 A US 2481859A
Authority
US
United States
Prior art keywords
fuel
ignition
cetane
diesel
alkyl
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
Application number
US694438A
Inventor
Miller Pharis
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Priority to US694438A priority Critical patent/US2481859A/en
Application granted granted Critical
Publication of US2481859A publication Critical patent/US2481859A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/1811Organic compounds containing oxygen peroxides; ozonides

Definitions

  • This invention relates to improved Diesel fuels and methods for preparing the same. More particularly, this invention relates to the incorporation of a novel type of ignition-promoting agent into a hydrocarbon Diesel fuel stock, such as a gas oil fraction of petroleum origin.
  • Hydrocarbon compounds characterized by aromatic hydrocarbons have poor ignition qualities which give rise to the vibrations manifested by knocking and result in a loss of power.
  • a poor ignition quality in a fuel is most frequently exhibited by an excessiv ignition lag, in other words, an excessive delay between the beginning of fuel injection into the combustion chamber of an engine and the point at which ignition of the injected fuel sets in.
  • normal aliphatic hydrocarbons have good ignition qualities.
  • Normal cetane, in'particular which serves as a standard of high ignition quality in Diesel fuel rating by recommendation of the S.
  • A. E. Volunteer Group forcompression-ignition fuel research has a very short ignition lag.
  • the ignition lag of a fuel consisting of cetane and alphamethyl-naphthalene is shortened very nearly in proportion to the increase in the percentage of cetane by volume in such a blend, and when small amounts of addition agents improve the performance of a fuel in the same respect comparable to the improvement made by an increase of about 5% or more of cetane in a blend with alphamethylmaphthalene, such addition agents have been considered as having commercial significance.
  • R may be hydrogen, alkyl, aryl or alkaryl and R may be alkyl, aryl or alkaryl.
  • Peroxides are well known as ignition promoters but all peroxides heretofore used have the disadvantage t that they are unstable and tend to deteriorate on storage so that Diesel fuels containing these compounds decrease in cetane number upon standing.
  • the peroxide esters of this invention may be prepared by reacting an acid chloride with an alkyl hydroperoxide in the presence of aqueous alkali in the cold.
  • alkyl hydroperoxide for example, tertiary butyl perbenzoate may be preparedby reacting t-butyl hydroperoxide with benzyl chloride in a 30% potassium hydroxide solution at a temperature of 10-20 C.
  • alkyl peresters may be prepared, such as alkyl perfuroate, aikyl perstearate, alkyl peêtcylenate, alkyl percrotonate, alkyl dipersuccinate, alkyl diperadipate, allryl diperphthalate and others.
  • the cetane number of a fuel is the per cent by volume of normal cetane in a blend consisting of normal cetane and alphamethyl naphthalene which gives comparable performance in the test engine and since the ignition lag of such a blend is shortened nearly in proportion to the increase in the volume percentage of the cetane, the cetane number change of a fuel is a measure of its ignition quality improvement when the cetane number change is positive.
  • the proportion of the ignition quality improving agent to be added to the hydrocarbon fuel may range from a fraction of one per cent to the limit of solubility in the fuel but preferably from about .025 to 5%.
  • a gas oil boiling from about 200 F. to 700 F'., or 750 F. or in general having a suitable boiling range for use as a fuel in Diesel type engines may be used as the hydrocarbon fuel under some circumstances, a more narrowly cut fraction such as one distilling from about 400 F. to 600 F. or from 500 F. to 700 F. may be used.
  • the hydrocarbon fuel may be said to have aboiling range above that of gasoline.
  • the e 'lectiveness of the peresters in raising the cetane number of'the fuel and in storage stability is illustrated comparing tests on an unmodified hydrocarbon Diesel oil with tests on samples of the same fuel modified by small amounts of a perester. Comparative tests are also shown of the effect of other types of peroxide ignition promoters.
  • the storage stability was obtained by allowing the fuel containing the promoter to stand over water in rusty iron pets at 125 F. for five weeks and ten weeks and then testing for cetane number and peroxide number.
  • This invention makes commercially feasible the preparation of Diesel fuels giving satisfactory engine performance from crude oils, gas oils and residual fuels having low pour points, low A. P. I. gravities and high heat Values, such as those procured from naphthene base, asphalt base or mixed base stocks by the addition of active perester compounds described in small quantities.
  • the burning qualities of gas oils from parafiln crudes are also enhanced by these novel addition agents.
  • Small quantities of the novel addition agents of this invention may be used for adapting various mixtures of hydrocarbons for use as Diesel fuels, including recycle stock from a cracking operation, non-parafllnic extracts, oils from destructive distillations of pyrobituminous and as phaltic materials, mixtures of these with one another or with crude petroleum fractions.
  • Other agents for enhancing various other qualities without detracting substantially from the ignition qualities of the fuel may be admixed, such as, oiliness agents, sludge dispersers, dyes, corrosion inhibitors, anti-oxidants, viscosity improvers, pour depressants and gum solvents. Also other promoters of ignition qualities may be admixed.
  • a fuel for compression ignition engines of the Diesel type consisting essentially of a hydrocarbon fuel which contains from about 025% to 5% of tertiary butyl perbenzoate.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (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 Sept. 13, 1949 I DIESEL FUEL Pharis Miller, Mountainside, N. J., assignor to pment Company, a cor- Standard Oil Develo poration of Delaware No Drawing. Application August 31,1946,
Serial No. 694,438
. 2 Claims. Y i
This invention relates to improved Diesel fuels and methods for preparing the same. More particularly, this invention relates to the incorporation of a novel type of ignition-promoting agent into a hydrocarbon Diesel fuel stock, such as a gas oil fraction of petroleum origin.
In consideration of increasing the power and fuel economy in the operation of compressionignition engines, principally when the hydrocarbon fuel contains insufficient amounts of hydrocarbon compounds recognizable as serving these ends by virtue of their suitable ignition qualities, the additions of various oxygenand nitrogencontaining organic compounds have been proposed.
Hydrocarbon compounds characterized by aromatic hydrocarbons have poor ignition qualities which give rise to the vibrations manifested by knocking and result in a loss of power. A poor ignition quality in a fuel is most frequently exhibited by an excessiv ignition lag, in other words, an excessive delay between the beginning of fuel injection into the combustion chamber of an engine and the point at which ignition of the injected fuel sets in. On the other hand, normal aliphatic hydrocarbons have good ignition qualities. Normal cetane, in'particular, which serves as a standard of high ignition quality in Diesel fuel rating by recommendation of the S. A. E. Volunteer Group forcompression-ignition fuel research, has a very short ignition lag. The ignition lag of a fuel consisting of cetane and alphamethyl-naphthalene is shortened very nearly in proportion to the increase in the percentage of cetane by volume in such a blend, and when small amounts of addition agents improve the performance of a fuel in the same respect comparable to the improvement made by an increase of about 5% or more of cetane in a blend with alphamethylmaphthalene, such addition agents have been considered as having commercial significance.
The novel addition agentsof the present invention are peresters characterized by the following typical structure:
0 R-gOO-R' where R may be hydrogen, alkyl, aryl or alkaryl and R may be alkyl, aryl or alkaryl. Peroxides are well known as ignition promoters but all peroxides heretofore used have the disadvantage t that they are unstable and tend to deteriorate on storage so that Diesel fuels containing these compounds decrease in cetane number upon standing.
The above class of compounds, however, have been found to be remarkably stable in storage and to increase the cetane number of Diesel fuels to which they are added to a point where they can be used in high speed engines.
The peroxide esters of this invention may be prepared by reacting an acid chloride with an alkyl hydroperoxide in the presence of aqueous alkali in the cold. For example, tertiary butyl perbenzoate may be preparedby reacting t-butyl hydroperoxide with benzyl chloride in a 30% potassium hydroxide solution at a temperature of 10-20 C.- Similarly other alkyl peresters may be prepared, such as alkyl perfuroate, aikyl perstearate, alkyl perundecylenate, alkyl percrotonate, alkyl dipersuccinate, alkyl diperadipate, allryl diperphthalate and others.
The manner of employing and testing the pere'sters for their ignition promoting properties is illustrated in the following description.
A number of samples were prepared by dissolving from a fraction of 0.5 to 2% by volume of the compound to be tested in a portion of a 37 octane number Colombian gas oil. Each sample was tested in a C. F. R. type Diesel engine according to the method disclosed in the S. A. E. Journal of June 1936,.page 225. By this test the ignition quality improvement imparted by the addition compound is noted in terms of cetane numbers obtained.
The cetane number of a fuel is the per cent by volume of normal cetane in a blend consisting of normal cetane and alphamethyl naphthalene which gives comparable performance in the test engine and since the ignition lag of such a blend is shortened nearly in proportion to the increase in the volume percentage of the cetane, the cetane number change of a fuel is a measure of its ignition quality improvement when the cetane number change is positive.
The proportion of the ignition quality improving agent to be added to the hydrocarbon fuel may range from a fraction of one per cent to the limit of solubility in the fuel but preferably from about .025 to 5%. A gas oil boiling from about 200 F. to 700 F'., or 750 F. or in general having a suitable boiling range for use as a fuel in Diesel type engines may be used as the hydrocarbon fuel under some circumstances, a more narrowly cut fraction such as one distilling from about 400 F. to 600 F. or from 500 F. to 700 F. may be used. Ordinarily, the hydrocarbon fuel may be said to have aboiling range above that of gasoline.
The e 'lectiveness of the peresters in raising the cetane number of'the fuel and in storage stability is illustrated comparing tests on an unmodified hydrocarbon Diesel oil with tests on samples of the same fuel modified by small amounts of a perester. Comparative tests are also shown of the effect of other types of peroxide ignition promoters. The storage stability was obtained by allowing the fuel containing the promoter to stand over water in rusty iron pets at 125 F. for five weeks and ten weeks and then testing for cetane number and peroxide number.
1 Gram mol. equivalents of active oxygen per 1000 liters of oil.
From the above data it is clear that 1% of the t-butyl perbenzoate is more effective in increasing the cetane number than either t-butyl hydroperoxide or l-hydroxy cyclohexyl-l-hydroperoxide and that furthermore it does not deteriorate in storage as do the other two peroxides.
This invention makes commercially feasible the preparation of Diesel fuels giving satisfactory engine performance from crude oils, gas oils and residual fuels having low pour points, low A. P. I. gravities and high heat Values, such as those procured from naphthene base, asphalt base or mixed base stocks by the addition of active perester compounds described in small quantities. The burning qualities of gas oils from parafiln crudes are also enhanced by these novel addition agents.
Small quantities of the novel addition agents of this invention may be used for adapting various mixtures of hydrocarbons for use as Diesel fuels, including recycle stock from a cracking operation, non-parafllnic extracts, oils from destructive distillations of pyrobituminous and as phaltic materials, mixtures of these with one another or with crude petroleum fractions. Other agents for enhancing various other qualities without detracting substantially from the ignition qualities of the fuel may be admixed, such as, oiliness agents, sludge dispersers, dyes, corrosion inhibitors, anti-oxidants, viscosity improvers, pour depressants and gum solvents. Also other promoters of ignition qualities may be admixed.
The nature and objects of the present invention having been thus described and illustrated, what is claimed as new and useful and is desired to be secured by Letters Patent is:
1. A fuel for compression ignition engines of the Diesel type consisting essentially of a hydrocarbon fuel which contains from about 025% to 5% of tertiary butyl perbenzoate.
2. Composition as defined by claim 1 wherein said hydrocarbon fuel boils in the range from about 200 F. to 750 F.
' PHARIS MILLER.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS ical Society, vol. 68, pages 642-644, April 1, 1946.
US694438A 1946-08-31 1946-08-31 Diesel fuel Expired - Lifetime US2481859A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US694438A US2481859A (en) 1946-08-31 1946-08-31 Diesel fuel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US694438A US2481859A (en) 1946-08-31 1946-08-31 Diesel fuel

Publications (1)

Publication Number Publication Date
US2481859A true US2481859A (en) 1949-09-13

Family

ID=24788825

Family Applications (1)

Application Number Title Priority Date Filing Date
US694438A Expired - Lifetime US2481859A (en) 1946-08-31 1946-08-31 Diesel fuel

Country Status (1)

Country Link
US (1) US2481859A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2618687A (en) * 1950-03-25 1952-11-18 Sperry Prod Inc Amplifier for rail flaw detector mechanisms
EP0467628A1 (en) * 1990-07-16 1992-01-22 Ethyl Petroleum Additives, Inc. Fuel compositions with enhanced combustion characteristics
US5114434A (en) * 1989-02-03 1992-05-19 Atochem Viscoreduced diesel fuels having improved cetane numbers
US5114433A (en) * 1989-03-14 1992-05-19 Atochem Directly distilled diesel fuels having improved cetane numbers
WO2010115900A1 (en) * 2009-04-06 2010-10-14 Bundesanstalt für Materialforschung und -Prüfung (BAM) Fuel and use thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2093008A (en) * 1934-06-29 1937-09-14 Egerton Alfred Charles Glyn Fuel for internal combustion engines
US2296558A (en) * 1938-09-20 1942-09-22 Autoxygen Inc Liquid fuel for internal combustion engines
US2403709A (en) * 1944-03-13 1946-07-09 Shell Dev Production of organic peroxides

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2093008A (en) * 1934-06-29 1937-09-14 Egerton Alfred Charles Glyn Fuel for internal combustion engines
US2296558A (en) * 1938-09-20 1942-09-22 Autoxygen Inc Liquid fuel for internal combustion engines
US2403709A (en) * 1944-03-13 1946-07-09 Shell Dev Production of organic peroxides

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2618687A (en) * 1950-03-25 1952-11-18 Sperry Prod Inc Amplifier for rail flaw detector mechanisms
US5114434A (en) * 1989-02-03 1992-05-19 Atochem Viscoreduced diesel fuels having improved cetane numbers
US5114433A (en) * 1989-03-14 1992-05-19 Atochem Directly distilled diesel fuels having improved cetane numbers
EP0467628A1 (en) * 1990-07-16 1992-01-22 Ethyl Petroleum Additives, Inc. Fuel compositions with enhanced combustion characteristics
US5405417A (en) * 1990-07-16 1995-04-11 Ethyl Corporation Fuel compositions with enhanced combustion characteristics
JP2902167B2 (en) 1990-07-16 1999-06-07 エチル・ペトロリアム・アデイテイブズ・インコーポレーテツド Fuel composition with enhanced combustion characteristics
WO2010115900A1 (en) * 2009-04-06 2010-10-14 Bundesanstalt für Materialforschung und -Prüfung (BAM) Fuel and use thereof

Similar Documents

Publication Publication Date Title
US2280217A (en) Super-diesel fuel
US2228662A (en) Motor fuel
RU2297443C2 (en) Light petroleum fuel
US2912313A (en) Diesel fuel
US2481859A (en) Diesel fuel
US2877102A (en) Diesel oil improvers
US2316011A (en) Fuels for internal combustion engines
US2225879A (en) Diesel fuel ignition promoter
US4294587A (en) Motor fuel
US2268382A (en) Ignition promotor for diesel fuels
US4647292A (en) Gasoline composition containing acid anhydrides
US3988122A (en) Motor fuel composition
US4600408A (en) Gasoline compositions containing carbonates
US5011503A (en) Fuel compositions
US5258049A (en) Diesel fuel composition
US2560602A (en) Fuel composition
US2324779A (en) Motor fuel
US3222146A (en) Glycerol esters in leaded gasoline
US4295861A (en) Motor fuel
US4602919A (en) Gasoline compositions containing malonates
US4740215A (en) Composition for cetane improvement of diesel fuels
RU2605952C1 (en) Alternative motor fuel and production method thereof
US3380815A (en) Cetane improver for diesel fuel oils
US2916366A (en) Motor fuel composition
US4341529A (en) Motor fuel