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 PDFInfo
- 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
- Authority
- 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
Links
- 239000002283 diesel fuel Substances 0.000 title claims abstract description 20
- 239000000203 mixture Substances 0.000 title claims abstract description 17
- RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 3
- 125000005843 halogen group Chemical group 0.000 claims abstract description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 claims description 15
- SJEBAWHUJDUKQK-UHFFFAOYSA-N 2-ethylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC=C3C(=O)C2=C1 SJEBAWHUJDUKQK-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 239000008096 xylene Substances 0.000 claims description 7
- 150000003738 xylenes Chemical class 0.000 claims description 7
- 239000001000 anthraquinone dye Substances 0.000 claims description 6
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 5
- 150000004056 anthraquinones Chemical class 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 3
- 239000000975 dye Substances 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 239000003921 oil Substances 0.000 description 15
- 239000000243 solution Substances 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 239000003550 marker Substances 0.000 description 6
- DMBHHRLKUKUOEG-UHFFFAOYSA-N N-phenyl aniline Natural products C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 4
- 239000003502 gasoline Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000004737 colorimetric analysis Methods 0.000 description 2
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 230000002110 toxicologic effect Effects 0.000 description 2
- 231100000027 toxicology Toxicity 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- -1 amino-aryl compound Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000004982 aromatic amines Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000013095 identification testing Methods 0.000 description 1
- 239000004434 industrial solvent Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000941 radioactive substance Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
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
- C10L1/003—Marking, e.g. coloration by addition of pigments
-
- 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
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1857—Aldehydes; 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.
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)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Lubricants (AREA)
Abstract
Description
- 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.
- 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:
- 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.
- 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 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.
- 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.
- 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.
- 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.
- 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 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.
-
Claims (8)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT2031685 | 1985-04-12 | ||
IT20316/85A IT1200452B (en) | 1985-04-12 | 1985-04-12 | DENATURING AND MARKING COMPOSITION, PARTICULARLY SUITABLE FOR DIESEL |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0201368A1 true EP0201368A1 (en) | 1986-11-12 |
EP0201368B1 EP0201368B1 (en) | 1989-07-19 |
Family
ID=11165673
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP86400642A Expired EP0201368B1 (en) | 1985-04-12 | 1986-03-26 | Marking and denaturing composition, particularly suitable for marking and denaturing diesel oil and similar oil products |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0201368B1 (en) |
DE (1) | DE3664476D1 (en) |
IT (1) | IT1200452B (en) |
Cited By (9)
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)
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 |
-
1985
- 1985-04-12 IT IT20316/85A patent/IT1200452B/en active
-
1986
- 1986-03-26 EP EP86400642A patent/EP0201368B1/en not_active Expired
- 1986-03-26 DE DE8686400642T patent/DE3664476D1/en not_active Expired
Patent Citations (5)
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 (14)
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 |
US12031098B2 (en) | 2019-12-03 | 2024-07-09 | Sicpa Holding Sa | Method of marking a petroleum hydrocarbon |
Also Published As
Publication number | Publication date |
---|---|
IT1200452B (en) | 1989-01-18 |
IT8520316A0 (en) | 1985-04-12 |
EP0201368B1 (en) | 1989-07-19 |
DE3664476D1 (en) | 1989-08-24 |
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