EP0201368A1 - Marking and denaturing composition, particularly suitable for marking and denaturing diesel oil and similar oil products - Google Patents

Marking and denaturing composition, particularly suitable for marking and denaturing diesel oil and similar oil products Download PDF

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Publication number
EP0201368A1
EP0201368A1 EP86400642A EP86400642A EP0201368A1 EP 0201368 A1 EP0201368 A1 EP 0201368A1 EP 86400642 A EP86400642 A EP 86400642A EP 86400642 A EP86400642 A EP 86400642A EP 0201368 A1 EP0201368 A1 EP 0201368A1
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EP
European Patent Office
Prior art keywords
marking
denaturing
anthraquinone
oil
diesel oil
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.)
Granted
Application number
EP86400642A
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German (de)
French (fr)
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EP0201368B1 (en
Inventor
Carlo Prandi
Alberto Osti
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.)
BASF Italia SpA
Original Assignee
PIGMENTI ITALIA SpA
PIGMENTI ITALIA SpA
BASF Italia SpA
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Publication of EP0201368A1 publication Critical patent/EP0201368A1/en
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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
    • C10L1/003Marking, e.g. coloration by addition of pigments
    • 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
    • C10L1/185Ethers; Acetals; Ketals; Aldehydes; Ketones
    • C10L1/1857Aldehydes; Ketones

Definitions

  • the Invention relates to a marking and denaturing composition, particularly suitable for marking and denaturing diesel oil and similar oil products.
  • U.S. patent 4 209 302 discloses the use of naphtylamine derivatives. However, these compounds do not completely satisfy the requirements herein-above, especially because they can easily be extracted from the marked product.
  • the invention concerns a marking and denaturing composition, particularly suitable for diesel oil and for similar oil products, containing an anthraquinone derivative having the formula: where R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 identical or different, represent a hydrogen atom, a halogen atom or an alkyl, cycloalkyl or arylalkyl radical having from 1 to 12 carbon atoms.
  • Oils products similar to diesel oil are, for example, gasoline, kerosene oil and lamp oil.
  • anthraquinone derivative to be used as a marker can vary within wide limits and the minimum value merely depends upon the identification test. By using the simple and rapid test described herein-after, concentrations as low as 1 to 3 ppm can be used.
  • a greater amount is added, in order to obtain in any case a positive result and also to foresee the case where the marked product is diluted at the time the fraud occurs. From a practical point of view, from 1 to 300 ppm (and preferably 3-50 ppm) can be used.
  • the markers according to the present invention should be prescribed, in particular, when an anthraquinone dye and/or an azoic dye is present; best results are obtained when using said markers or marking compositions in admixture with furfural and/or with other suitable organic solvents, for example xylenes, these xylenes generally acting as a diluent.
  • Example 1 was repeated, by carrying out the test on the same diesel oil, without any admixture of the marking solution, the final bottom layer was light brown.
  • Example 6 was repeated while replacing gasoline by lamp oil to be used for the lighting of fishing boats.
  • the final bottom aqueous layer obtained also presented a deep red color.
  • Example 1 was repeated while modifying the chemical nature of the marker and its concentration; data and results are on table 1.

Abstract

The invention relates to a marking and denaturing composition, particularly suitable for marking and denaturing diesel oil and similar oil products.
The said composition contains an anthraquinone derivative having the formula:
Figure imga0001
where R1, R2, R3, R4, R5, R6, R7 and R8 identical or different, represent a hydrogen atom, a halogen atom or an alkyl, cycloalkyl or arylalkyl radical having from 1 to 12 carbon atoms.

Description

    BACKGROUND OF THE INVENTION
  • The Invention relates to a marking and denaturing composition, particularly suitable for marking and denaturing diesel oil and similar oil products.
  • There is currently a need for marking oil products (for example fuels or industrial solvents) due to the difference in price at which that same product may be offered for sale. Indeed, as a consequence of different rates of taxation, diesel oils intended e.g. for agricultural purposes, or diesel oils intended for the fishing industry are taxed at a lower rate than diesel oil intended for road vehicles and such a situation is liable to give rise to fiscal fraud, when the product is furnished for purposes different to those provided for by the fiscal regulations. This is in fact why the products are usually marked by means of suitable compounds, which allow an easy identification. An ideal marker or marking composition should exhibit the following features:
    • - a satisfactory stability under conditions of normal use;
    • - no impairing of the physico-chemical features of the petroleum fuel or of the solvent;
    • - a solubility sufficient to allow use in the form of a concentrated solution;
    • - very low chances of being eliminated by means of physical or chemical methods;
    • - possibility of being used in small quantities;
    • - possibility of being identified by means of simple, quick and very sensitive methods;
    • - absence of negative toxicological features.
  • Not all proposed or used marking compositions can completely satisfy such requirements. In fact, the best known markers are:
    • - radioactive substances, requiring particular care, during handling, because of physiological dangers;
    • - metallorganic compounds, generally showing a poor stability during storage;
    • - furfural, which could also be present as traces naturally occurring in the oil cuts, and thus give rise to a positive test due simply to the particular kind of analysis (furfural, moreover, shows poor stability);
    • - diphenylamine, which can be rather easily eliminated; since it is an amino-aryl compound, diphenylamine must be handled in a carefully strictly controlled zone;
    • - primary, secondary or tertiary arylamines, which can easily be extracted by means of diluted acids; as with the case of diphenylamine, their handling is controlled by very strict regulations;
    • - naphthols, which could already be present within the oil cuts and which can easily be eliminated.
  • U.S. patent 4 209 302 discloses the use of naphtylamine derivatives. However, these compounds do not completely satisfy the requirements herein-above, especially because they can easily be extracted from the marked product.
  • The applicant has now found a new marking composition allowing an unexpected and unforeseen reduction of the drawbacks herein-above.
  • DISCLOSURE OF THE INVENTION
  • In its widest form the invention concerns a marking and denaturing composition, particularly suitable for diesel oil and for similar oil products, containing an anthraquinone derivative having the formula:
    Figure imgb0001
    where R1, R2, R3, R4, R5, R6, R7 and R8 identical or different, represent a hydrogen atom, a halogen atom or an alkyl, cycloalkyl or arylalkyl radical having from 1 to 12 carbon atoms.
  • Oils products similar to diesel oil are, for example, gasoline, kerosene oil and lamp oil.
  • The amounts of anthraquinone derivative to be used as a marker can vary within wide limits and the minimum value merely depends upon the identification test. By using the simple and rapid test described herein-after, concentrations as low as 1 to 3 ppm can be used.
  • Generally, a greater amount is added, in order to obtain in any case a positive result and also to foresee the case where the marked product is diluted at the time the fraud occurs. From a practical point of view, from 1 to 300 ppm (and preferably 3-50 ppm) can be used.
  • The advantages inherent within the present anthraquinone derivative having formula (I) are the following:
    • - no counter-indications of toxicological nature;
    • - considerable stability with respect to the oil product to be marked;
    • - difficulty to eliminate the said marker from its solutions within the oil products, by means, for example, of adsorption techniques on active carbons, alumina, decoloring earth or silica gel;
    • - no modification of color of the oil product, whereby the presence within diesel oil can be ascertained only when carrying out a specific test;
    • - it can be identified and determined quantitatively by means of very simple methods that do not require complicated devices and can be carried out by unskilled personnel;
    • - it can be handled either as a solid or as a solution in organic solvents, optionally in admixture with other colored or colorless markers.
  • The markers according to the present invention should be prescribed, in particular, when an anthraquinone dye and/or an azoic dye is present; best results are obtained when using said markers or marking compositions in admixture with furfural and/or with other suitable organic solvents, for example xylenes, these xylenes generally acting as a diluent.
  • As to the mothod of identifying the products it is preferable to operate according to the following method:
    • - 10 cm3 of acetone and 5 cm3 of an aqueous and alkaline solution of sodium dithionite are added to 200 cm3 of marked diesel oil which is thereafter stirred and left to decant for 5-10 minutes, whereby the bottom layer presents a red color characteristic of the anthraquinone derivative according to formula (I).
  • The following examples illustrate the invention, without however in any way limiting its scope.
  • EXAMPLE 1
  • 1 g of 2-ethyl-anthraquinone was added to 100 cm3 of a mixture of xylenes and to 3 cm3 of the solution thus obtained a diesel oil,intended for motorboats, was added until 1 liter volume was obtained, i.e. a solution containing 30 mg/dm3 (30 ppm) of 2-ethyl-anthraquinone. Thereafter, 10 cm3 of acetone and 5 cm3 of an aqueous solution containing 15% by weight of Na2S204 in aqueous NaOH (10% by weight) were added to 200 cm3 of the diesel oil marked as above; after stirring for 20 seconds, the solution was decanted for 10 minutes, thereby obtaining a deep red aqueous layer on the bottom.
  • EXAMPLE 2 (Blank, comparative example)
  • Example 1 was repeated, by carrying out the test on the same diesel oil, without any admixture of the marking solution, the final bottom layer was light brown.
  • EXAMPLE 3
  • 100 cm3 of diesel oil, marked as in example 1, were admixed with 900 cm3 of previously unmarked diesel oil, thus reducing the amount of marker to 3 mg/dm3; the colorimetric test caused formation of a final bottom layer still red,the intensity of which was much lower than that obtained in example 1.
  • EXAMPLE 4
  • 100 cm3 of unmarked diesel oil, 20 cm3 of acetone and 10 cm3 of the dithionite solution of example 1 were added to 100 cm3 of diesel oil marked as in example 1; after stirring and decanting, the bottom phase was collected in a volumetric flask. The absorption intensity, after filtration, was determined at 50 nm (nanometer). A calibration plot allowed to confirm with precision the original marker concentration.
  • EXAMPLE 5
  • 1 g of a composition, obtained by mixing 8 g of 2-ethyl-anthraquinone, 8 g of furfural, 64.8 g of an anthraquinone dye (known according to the COLOR INDEX as "solvent green 33"), and 7.2 g of mixed xylenes, were added to 4 kg of a diesel oil to be used for motorboats, thus obtaining a fuel containing 20 ppm of 2-ethyl-anthraquinone. The colorimetric test of example 1 was carried out on 200 cm3 of the thus marked oil and an aqueous bottom layer presenting a deep red color was obtained.
  • EXAMPLE 6
  • 1 g of 2-ethyl-anthraquinone was added to 100 cm3 of a mixture of xylenes and to 3 cm3 of the thus obtained xylenic solution a gasoline to be used for motorboats in the fishing industry was added until the obtention of a 1 liter volume. The resulting solution contained 30 mg/dm3 of 2-ethyl-anthraquinone. Thereafter, 100 cm3 of virgin (unmarked) diesel oil, 10 cm3 of acetone and 5 cm3 of the dithionite solution of example 1 were added to 100 cm3 of gasoline marked as above; the test was operated as in example 1 and a deep red aqueous layer was obtained on the bottom.
  • EXAMPLE 7
  • Example 6 was repeated while replacing gasoline by lamp oil to be used for the lighting of fishing boats. In this case the final bottom aqueous layer obtained also presented a deep red color.
  • EXAMPLES 8-14
  • Example 1 was repeated while modifying the chemical nature of the marker and its concentration; data and results are on table 1.
    Figure imgb0002

Claims (8)

1.- A marking and denaturing composition, particularly suitable for marking and denaturing oil and similar oil products, containing an anthraquinone derivative having the formula:
Figure imgb0003
where R1, R21 R35 R4, R5, R5, R7 and R8 identical or different, represent a hydrogen atom, a halogen atom or an alkyl, cycloalkyl or arylalkyl radical having from 1 to 12 carbon atoms.
2.- Composition according to claim 1, also containing a usual dye for oil products, in particular an azoic dye and/or an anthraquinone dye.
3.- Composition according to claim 1, also containing as a diluent furfural and/or suitable organic solvents, for example xylenes.
4.- A marking and denaturing composition suitable for marking diesel oil, containing 2-ethyl-anthraquinone and preferably further containing a suitable organic solvent as a diluent.
5.- Composition according to claim 4, further containing furfural and/or an anthraquinone dye.
6.- Marked diesel oil containing from 1 to 300 ppm and preferably from 3 to 50 ppm of 2-ethyl-anthraquinone, preferably in admixture with furfural and/or with an anthraquinone dye.
7.- A method for marking and/or denaturing diesel oil or other similar oil product, wherein the anthraquinone derivative of claim 1 is added to the product to be marked and/or denatured, preferably in admixture with furfural, with an anthraquinone dye and with a proper solvent, for example xylenes.
8.- A method according to claim 7, wherein the amount of said anthraquinone derivative is comprised between 1 and 300 ppm, and preferably between 3 and 50 ppm, with respect to the oil product to be marked and/or denatured.
EP86400642A 1985-04-12 1986-03-26 Marking and denaturing composition, particularly suitable for marking and denaturing diesel oil and similar oil products Expired EP0201368B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT20316/85A IT1200452B (en) 1985-04-12 1985-04-12 DENATURING AND MARKING COMPOSITION, PARTICULARLY SUITABLE FOR DIESEL
IT2031685 1985-04-12

Publications (2)

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EP0201368A1 true EP0201368A1 (en) 1986-11-12
EP0201368B1 EP0201368B1 (en) 1989-07-19

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DE (1) DE3664476D1 (en)
IT (1) IT1200452B (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1001003A1 (en) * 1998-11-09 2000-05-17 Morton International, Inc. Method for invisibly tagging petroleum products using visible dyes
EP1323811A2 (en) * 2001-12-20 2003-07-02 Rohm And Haas Company Method for marking hydrocarbons with anthraquinones
WO2005063942A1 (en) * 2003-12-23 2005-07-14 Basf Aktiengesellschaft Power and lubricant additive concentrates containing at least one anthrachinone derivative as a marking substance
US6977177B1 (en) 2004-05-26 2005-12-20 Rohm And Haas Company Method for marking hydrocarbons with substituted anthraquinones
US7157611B2 (en) 2002-07-11 2007-01-02 Rohm And Haas Company Pyrazinoporphyrazines as markers for liquid hydrocarbons
CN1321965C (en) * 2005-07-22 2007-06-20 清华大学 Anthraquinone derivative and its synthesis method
US7635596B2 (en) 2004-12-15 2009-12-22 Rohm And Haas Company Method for monitoring degradation of lubricating oils
US7915048B2 (en) 2003-06-13 2011-03-29 Rohm And Haas Company Method for marking hydrocarbons with substituted anthraquinones
WO2021110526A1 (en) 2019-12-03 2021-06-10 Sicpa Holding Sa Method of marking a petroleum hydrocarbon

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE524604A (en) *
GB361310A (en) * 1930-06-18 1931-11-18 Howard Ferguson Improvements in and relating to motor fuels or like combustible liquids
GB851639A (en) * 1958-09-26 1960-10-19 Exxon Research Engineering Co Improved hydrocarbon oils
US3164449A (en) * 1961-03-01 1965-01-05 Du Pont Anthraquinone dyes for gasoline
DE2702985C2 (en) * 1977-01-26 1979-02-15 Basf Ag, 6700 Ludwigshafen Process for the production of opaque pyranthrone pigments

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE524604A (en) *
GB361310A (en) * 1930-06-18 1931-11-18 Howard Ferguson Improvements in and relating to motor fuels or like combustible liquids
GB851639A (en) * 1958-09-26 1960-10-19 Exxon Research Engineering Co Improved hydrocarbon oils
US3164449A (en) * 1961-03-01 1965-01-05 Du Pont Anthraquinone dyes for gasoline
DE2702985C2 (en) * 1977-01-26 1979-02-15 Basf Ag, 6700 Ludwigshafen Process for the production of opaque pyranthrone pigments

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6274381B1 (en) 1998-11-09 2001-08-14 Rohm And Haas Company Method for invisibly tagging petroleum products using visible dyes
EP1001003A1 (en) * 1998-11-09 2000-05-17 Morton International, Inc. Method for invisibly tagging petroleum products using visible dyes
EP1323811A2 (en) * 2001-12-20 2003-07-02 Rohm And Haas Company Method for marking hydrocarbons with anthraquinones
EP1323811A3 (en) * 2001-12-20 2003-12-03 Rohm And Haas Company Method for marking hydrocarbons with anthraquinones
US6811575B2 (en) 2001-12-20 2004-11-02 Rohm And Haas Company Method for marking hydrocarbons with anthraquinones
US7157611B2 (en) 2002-07-11 2007-01-02 Rohm And Haas Company Pyrazinoporphyrazines as markers for liquid hydrocarbons
US7915048B2 (en) 2003-06-13 2011-03-29 Rohm And Haas Company Method for marking hydrocarbons with substituted anthraquinones
AU2004309053B2 (en) * 2003-12-23 2010-06-10 Basf Aktiengesellschaft Power and lubricant additive concentrates containing at least one anthrachinone derivative as a marking substance
WO2005063942A1 (en) * 2003-12-23 2005-07-14 Basf Aktiengesellschaft Power and lubricant additive concentrates containing at least one anthrachinone derivative as a marking substance
US6977177B1 (en) 2004-05-26 2005-12-20 Rohm And Haas Company Method for marking hydrocarbons with substituted anthraquinones
US7635596B2 (en) 2004-12-15 2009-12-22 Rohm And Haas Company Method for monitoring degradation of lubricating oils
CN1321965C (en) * 2005-07-22 2007-06-20 清华大学 Anthraquinone derivative and its synthesis method
WO2021110526A1 (en) 2019-12-03 2021-06-10 Sicpa Holding Sa Method of marking a petroleum hydrocarbon

Also Published As

Publication number Publication date
DE3664476D1 (en) 1989-08-24
EP0201368B1 (en) 1989-07-19
IT8520316A0 (en) 1985-04-12
IT1200452B (en) 1989-01-18

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