EP0311790A1 - Marked mineral oil product, and process to mark mineral oil products - Google Patents
Marked mineral oil product, and process to mark mineral oil products Download PDFInfo
- Publication number
- EP0311790A1 EP0311790A1 EP88114751A EP88114751A EP0311790A1 EP 0311790 A1 EP0311790 A1 EP 0311790A1 EP 88114751 A EP88114751 A EP 88114751A EP 88114751 A EP88114751 A EP 88114751A EP 0311790 A1 EP0311790 A1 EP 0311790A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- mineral oil
- oil product
- marked
- marking
- color former
- 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.)
- Withdrawn
Links
- 0 CC(C1C2C3C(*)=CC=CC3)=NC(*)=NC1OC1=C2C=CC(*)C1 Chemical compound CC(C1C2C3C(*)=CC=CC3)=NC(*)=NC1OC1=C2C=CC(*)C1 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
Definitions
- Mineral oil products are often colored and marked to indicate quality, in particular to demonstrate that tax-privileged mineral oil products are used illegally. While the dye is directly recognizable by its color, the marking agent is colorless. This can only be made visible by special treatment, so that the type and amount of marking agent can be determined.
- the invention relates to a marked mineral oil product, which is characterized in that the mineral oil product contains at least one color former as a marking agent.
- the marking agent can still be reliably detected in concentrations of 0.5 ppm.
- the mineral oil product labeled according to the invention advantageously contains at least a multiple of the still detectable amount of color former, i.e. expediently about 1 ppm up to 100 ppm, in particular 1 to 50 ppm.
- the marking agent according to the invention can be detected qualitatively and quantitatively.
- the color formers used as marking agents are detected either by shaking the mineral oil product with naphthol-2 or with alcoholic aqueous hydrochloric acid or by immersing a test strip containing an acidic agent in the mineral oil product to be tested.
- the test strip can e.g. B. be prepared by preparing a strip of filter paper with alcoholic aqueous hydrochloric acid. It can also with acidic earth z. B. montmorillonite, coated absorbent papers can be used.
- Color formers are understood to mean compounds which are colorless but form dyes or give colorations in contact with acidic compounds.
- Color formers are known from the production of carbonless carbonless papers. For this application, the color formers are usually applied to the paper in the form of a solution enclosed in microcapsules.
- color formers such.
- Diazarhodamine lactones e.g. those described in DE-OS 22 43 483 and 25 09 793 preferred because of their high reactivity and the high color strength of the dyeings formed with electron acceptors.
- the marked mineral oil products according to the invention are advantageously produced by adding solutions of the color formers (marking mixtures), the marking mixture being added in an amount such that the mineral oil products contain the desired content of marking agent (color formers).
- the marking mixtures contain the color former (s) in dissolved form in a solvent suitable for the intended application, in which the color former should be readily soluble.
- z. B. toluene For the marking of mineral oil products, z. B. toluene, the xylenes, high-boiling aromatics such as Shellsol AB or Solvesso and other solvents compatible with the mineral oil products, such as acetone or mixtures thereof, are well suited.
- the concentration of the color former in the marking mixture is selected such that a stable stock solution is present and that a reliable marking is achieved by metering the marking mixture into the mineral oil product using existing metering devices.
- concentrations of color former in the marking mixtures are advantageously 1 to 20% by weight, generally 5 to 15% by weight, depending on how soluble the color former is in the solvent.
- the invention is further illustrated by the following examples.
- the parts specified are parts by weight and the percentages relate to the weight.
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)
- Color Printing (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
Mineralölprodukte werden häufig zur Kennzeichnung der Qualität, insbesondere zum Nachweis von gesetzeswidrig verwendeten steuerbegünstigten Mineralölprodukten gefärbt und markiert. Während der Farbstoff durch seine Farbe direkt erkennbar ist, ist das Markierungsmittel farblos. Dieses kann nur durch eine besondere Behandlung sichtbar gemacht werden, so daß Art und Menge an Markierungsmittel bestimmt werden können.Mineral oil products are often colored and marked to indicate quality, in particular to demonstrate that tax-privileged mineral oil products are used illegally. While the dye is directly recognizable by its color, the marking agent is colorless. This can only be made visible by special treatment, so that the type and amount of marking agent can be determined.
So wird z. B. in der Bundesrepublik Deutschland Heizöl nach § 15, Abs. 2 des Mineralsteuergesetzes und der Rechtsverordnung vom 09.11.1977 mit C.I. Solvent Red 19; C.I. Nr. 26050 oder einem Gemisch aus den Kupplungsprodukten von diazotiertem 4-Aminoazobenzol auf ein Gemisch aus 2-(2′-Ethylhexyamino)-naphthalin und 2-Tridecylaminonaphthalin in Kombination mit Furfurol gekennzeichnet.So z. B. in the Federal Republic of Germany heating oil according to § 15, paragraph 2 of the Mineral Tax Act and the ordinance of November 9, 1977 with C.I. Solvent Red 19; C.I. No. 26050 or a mixture of the coupling products of diazotized 4-aminoazobenzene on a mixture of 2- (2'-ethylhexyamino) naphthalene and 2-tridecylaminonaphthalene in combination with furfural.
Aufgabe der vorliegenden Erfindung war es, ein einfach anwendbares Verfahren zur Markierung von Mineralölprodukten bereitzustellen, wobei in den markierten Produkten das oder die Markierungsmittel einfach und sicher nachgewiesen werden können.It was an object of the present invention to provide an easy-to-use method for marking mineral oil products, the marking product (s) being able to be detected simply and reliably in the marked products.
Die Erfindung betrifft ein markiertes Mineralölprodukt, das dadurch gekennzeichnet ist, daß das Mineralölprodukt mindestens einen Farbbildner als Markierungsmittel enthält.The invention relates to a marked mineral oil product, which is characterized in that the mineral oil product contains at least one color former as a marking agent.
In dem erfindungsgemäß markierten Mineralölprodukt kann das Markierungsmittel noch in Konzentrationen von 0,5 ppm sicher nachgewiesen werden.In the mineral oil product marked according to the invention, the marking agent can still be reliably detected in concentrations of 0.5 ppm.
Das erfindungsgemäß markierte Mineralölprodukt enthält vorteilhafterweise mindestens ein Mehrfaches der noch nachweisbaren Menge an Farbbildner, d.h. zweckmäßigerweise etwa 1 ppm bis zu 100 ppm, insbesondere 1 bis 50 ppm.The mineral oil product labeled according to the invention advantageously contains at least a multiple of the still detectable amount of color former, i.e. expediently about 1 ppm up to 100 ppm, in particular 1 to 50 ppm.
Wird das so markierte Mineralölprodukt mit nicht oder anders gekennzeichnetem Produkt verschnitten, dann ist das erfindungsgemäße Markierungsmittel qualitativ und quantitativ nachweisbar.If the mineral oil product labeled in this way is blended with a product that is not labeled or labeled otherwise, the marking agent according to the invention can be detected qualitatively and quantitatively.
Der Nachweis der als Markierungsmittel verwendeten Farbbildner erfolgt entweder durch Ausschütteln des Mineralölproduktes mit Naphthol-2 oder mit alkoholisch wäßriger Salzsäure oder auch durch Eintauchen eines ein saures Mittel enthaltenden Teststreifens in das zu prüfende Mineralölprodukt. Der Teststreifen kann z. B. durch Präpieren eines Streifens Filterpapier mit alkoholisch wäßriger Salzsäure hergestellt werden. Es können auch mit sauren Erden z. B. Montmorillonit, beschichtete saugfähige Papiere verwendet werden.The color formers used as marking agents are detected either by shaking the mineral oil product with naphthol-2 or with alcoholic aqueous hydrochloric acid or by immersing a test strip containing an acidic agent in the mineral oil product to be tested. The test strip can e.g. B. be prepared by preparing a strip of filter paper with alcoholic aqueous hydrochloric acid. It can also with acidic earth z. B. montmorillonite, coated absorbent papers can be used.
Unter Farbbildner werden Verbindungen verstanden, die farblos sind, jedoch in Kontakt mit sauren Verbindungen Farbstoffe bilden, bzw. Färbungen geben. Farbbildner sind aus der Herstellung von kohlefreien Durchschreibepapieren bekannt. Für diese Anwendung werden die Farbbildner meistens in Form einer in Mikrokapseln eingeschlossenen Lösung auf das Papier aufgebracht. Als Farbbildner kommen z. B. solche aus der Gruppe der Lactone, wie Kristallviolettlacton, der Fluorane wie Fluoranlactone, Rhodaminlactone, Diazarhodaminlactone, der Phthalide, der Spirodipyrane wie Dibenzodipyrane oder Gemische dieser Verbindungen in Betracht. Hinsichtlich der Farbbildner sei auf die folgende Literatur hingewiesen:
DE-OS 16 71 545, 20 24 859, 21 30 845, 21 30 846, 21 55 987, 24 22 899, 22 43 483, 23 23 803, 24 24 935, 22 62 127, 22 02 315, 21 22 997, 21 55 997, 24 30 568, 25 09 793, 26 11 600, 31 14 968 und 33 37 387; JP-A-273/1977; GB-A-20 97 013 und EP-A-10 740.Color formers are understood to mean compounds which are colorless but form dyes or give colorations in contact with acidic compounds. Color formers are known from the production of carbonless carbonless papers. For this application, the color formers are usually applied to the paper in the form of a solution enclosed in microcapsules. As color formers such. B. from the group of lactones, such as crystal violet lactone, fluoranes such as fluoranlactones, rhodamine lactones, diazarhodamine lactones, phthalides, spirodipyrans such as dibenzodipyrans or mixtures of these compounds. With regard to the color formers, reference is made to the following literature:
DE-OS 16 71 545, 20 24 859, 21 30 845, 21 30 846, 21 55 987, 24 22 899, 22 43 483, 23 23 803, 24 24 935, 22 62 127, 22 02 315, 21 22 997 , 21 55 997, 24 30 568, 25 09 793, 26 11 600, 31 14 968 and 33 37 387; JP-A-273/1977; GB-A-20 97 013 and EP-A-10 740.
Als Markierungsmittel sind Diazarhodaminlactone, z.B. die in den DE-OS 22 43 483 und 25 09 793 beschriebenen, wegen ihrer hohen Reaktionsfähigkeit und der hohen Farbstärke der mit Elektronacceptoren gebildeten Färbungen bevorzugt.Diazarhodamine lactones, e.g. those described in DE-OS 22 43 483 and 25 09 793 preferred because of their high reactivity and the high color strength of the dyeings formed with electron acceptors.
Die erfindungsgemäßen markierten Mineralölprodukte werden vorteilhafterweise durch Zugeben von Lösungen der Farbbildner (Markierungsgemische) hergestellt, wobei das Markierungsgemisch in einer Menge zugegeben wird, daß die Mineralölprodukte den gewünschten Gehalt an Markierungsmittel (Farbbildner) enthalten.The marked mineral oil products according to the invention are advantageously produced by adding solutions of the color formers (marking mixtures), the marking mixture being added in an amount such that the mineral oil products contain the desired content of marking agent (color formers).
Die Markierungsgemische enthalten den oder die Farbbildner in gelöster Form in einem für die vorgesehene Anwendung geeigneten Lösungsmittel, in dem der Farbbildner gut löslich sein sollte.The marking mixtures contain the color former (s) in dissolved form in a solvent suitable for the intended application, in which the color former should be readily soluble.
Für die Markierung von Mineralölprodukten sind als Lösungsmittel z. B. Toluol die Xylole, hochsiedende Aromaten wie Shellsol AB oder Solvesso und andere mit den Mineralölprodukten verträgliche Lösungsmittel wie Aceton oder Gemische davon gut geeignet.For the marking of mineral oil products, z. B. toluene, the xylenes, high-boiling aromatics such as Shellsol AB or Solvesso and other solvents compatible with the mineral oil products, such as acetone or mixtures thereof, are well suited.
Die Konzentration des Farbbildners in dem Markierungsgemisch wird so gewählt - daß eine stabile Stammlösung vorliegt und -, daß eine sichere Markierung durch Zudosieren des Markierungsgemisches zum Mineralölprodukt mit vorhandenen Dosiereinrichtungen erreicht wird.The concentration of the color former in the marking mixture is selected such that a stable stock solution is present and that a reliable marking is achieved by metering the marking mixture into the mineral oil product using existing metering devices.
Vorteilhafterweise liegen die Konzentrationen an Farbbildner in den Markierungsgemischen bei 1 bis 20 Gew.%, in der Regel bei 5 bis 15 Gew.%, je nachdem wie löslich der Farbbildner in dem Lösungsmittel ist.The concentrations of color former in the marking mixtures are advantageously 1 to 20% by weight, generally 5 to 15% by weight, depending on how soluble the color former is in the solvent.
Zur Markierung wird dem Mineralölprodukt soviel Gemisch zugegeben, daß das Produkt die angegebenen Mengen an Farbbildner enthält.Sufficient mixture is added to the mineral oil product for marking that the product contains the stated amounts of color former.
Die Erfindung soll durch die folgenden Ausführungsbeispiele zusätzlich erläutert werden. Die angegebenen Teile sind Gewichtsteile und die Prozentangaben beziehen sich auf das Gewicht.The invention is further illustrated by the following examples. The parts specified are parts by weight and the percentages relate to the weight.
- a) Zu 1000 Teilen Mineralöl werden 0,1 Teile des unter c) beschriebenen Markierungsgemischs gegeben und gemischt. Das markierte Mineralöl war farblos. Die Konzentration an Farbbildner beträgt 10 ppm. Ein in diese Lösung getauchter Papierstreifen, der mit alkoholisch-wäßriger 10 %iger Salzsäure imprägniert ist, färbt sich intensiv rot.a) 0.1 part of the marking mixture described under c) is added to 1000 parts of mineral oil and mixed. The marked mineral oil was colorless. The concentration of color former is 10 ppm. A paper strip dipped in this solution, which is impregnated with alcoholic-aqueous 10% hydrochloric acid, turns intensely red.
-
b) Das markierte Mineralöl von a) wurde mit dem 20fachen Volumen nicht markierten Mineralöls verdünnt, d. h. der Gehalt an Farbbildner beträgt jetzt 0,5 ppm.
Auch in diesem Gemisch ist der Farbbildner durch Färbung des oben angegebenen Teststreifens einwandfrei zu erkennen und nachzuweisen.
Bei noch geringeren Konzentrationen an Markierungsmittel, z.B. durch Verdünnen des nach a) erhaltenen markierten Mineralöl mit den 40-fachen Volumen nicht markierten Mineralöls, ist der Nachweis dadurch möglich, daß das zu prüfende Mineralöl mehrmals auf die gleiche Stelle des Teststreifens aufgetropft wird. Vorteilhafterweise verwendet man in diesem Fall als Teststreifen eine mit saurem Clay beschichtete Platte für die Dünnschichtchromatographie.b) The marked mineral oil from a) was diluted with 20 times the volume of unmarked mineral oil, ie the color former content is now 0.5 ppm.
In this mixture, too, the color former can be recognized and detected perfectly by coloring the test strip specified above.
In the case of even lower concentrations of marking agent, for example by diluting the marked mineral oil obtained according to a) with 40 times the volume of unmarked mineral oil, it is possible to prove that the mineral oil to be tested is dripped onto the same area of the test strip several times. In this case, an acid clay-coated plate for thin-layer chromatography is advantageously used as the test strip. -
c) Markierungsgemisch
100 g Lacton der Formel
100 g lactone of the formula
- a) Erdöldestillat (Benzinschnitt) wurde mit den in der Tabelle angegebenen Farbbildner markiert. Es wurden jeweils soviel der nach c) hergestellten Lösung zugegeben, daß das Mineralölprodukt 5 ppm des Markierungsmittels enthielt.a) Petroleum distillate (gasoline cut) was marked with the color formers given in the table. So much of the solution prepared according to c) was added that the mineral oil product contained 5 ppm of the marking agent.
-
b) Nachweis des Markierungsmittels im Mineralölprodukt (Benzin) 20 ml des markierten Produktes wurden in einer Flasche mit 2 g Silicagel versetzt und das Ganze geschüttelt. Spontan entsteht auf dem vorher farblosen Kieselgel eine intensive Färbung, die deutlich zu erkennen ist. Die Farbe ist abhängig von dem verwendeten Farbbildner.
Nach dem Absetzen des Silicagels ist der Farbeindruck und die Farbstärke deutlich intensiver. Nach dem Absetzen des Silicagels kann die Färbung mit einer Blindprobe verglichen werden.
Auf diese Weise kann die Färbung des Silicagels auch bei dunklen Mineralölprodukten sicher erkannt werden.b) Detection of the marking agent in the mineral oil product (petrol) 20 ml of the marked product were mixed with 2 g of silica gel in a bottle and the whole was shaken. Spontaneously an intense coloration develops on the previously colorless silica gel, which is clearly recognizable. The color depends on the color former used.
After the silica gel has been removed, the color impression and the color strength are significantly more intense. After the silica gel has settled, the staining can be compared with a blank sample.
In this way, the color of the silica gel can be reliably recognized even with dark mineral oil products. - c) Das zur Markierung verwendete Markierungsgemisch wurde durch Lösen von 1 g der in der Tabelle Spalte 1 genannten Farbbildner (Markierungsmittel) in 9 g Toluol hergestellt (10%ige Lösung).c) The marking mixture used for the marking was prepared by dissolving 1 g of the color formers (marking agents) mentioned in the table in column 1 in 9 g of toluene (10% strength solution).
Claims (9)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19873731458 DE3731458A1 (en) | 1987-09-18 | 1987-09-18 | MARKING MIXTURE FOR LABELING MINERAL OIL PRODUCTS AND MARKED MINERAL OIL PRODUCTS |
DE3731458 | 1987-09-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0311790A1 true EP0311790A1 (en) | 1989-04-19 |
Family
ID=6336353
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88114751A Withdrawn EP0311790A1 (en) | 1987-09-18 | 1988-09-09 | Marked mineral oil product, and process to mark mineral oil products |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0311790A1 (en) |
JP (1) | JPH01104692A (en) |
AU (1) | AU606993B2 (en) |
DE (1) | DE3731458A1 (en) |
FI (1) | FI884247A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0438734A1 (en) * | 1990-01-22 | 1991-07-31 | BASF Aktiengesellschaft | Marked mineral oils and process to mark mineral oils by means of basic dyes |
EP0490232A1 (en) * | 1990-12-14 | 1992-06-17 | BASF Aktiengesellschaft | Device for detecting marked mineral oils |
US5882358A (en) * | 1995-06-07 | 1999-03-16 | United Color Manufacturing, Inc. | Colored transmission fluid |
EP1001003A1 (en) * | 1998-11-09 | 2000-05-17 | Morton International, Inc. | Method for invisibly tagging petroleum products using visible dyes |
WO2000059751A1 (en) * | 1999-04-06 | 2000-10-12 | Imperial Chemical Industries Plc | Reservoir combination for flammable fluids |
WO2003078551A2 (en) * | 2002-03-15 | 2003-09-25 | Shell Internationale Research Maatschappij B.V. | Oil composition and method of detecting a marker in an oil composition |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100914259B1 (en) * | 2008-12-15 | 2009-08-27 | 오리엔트화학 (주) | Marker for oil identification using a metal complex dye coloring agent, oil identification method using the marker |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB357179A (en) * | 1930-06-17 | 1931-09-17 | Patent Fuels & Color Corp | Improvements in the art of colouring gasoline or other petroleum distillates |
GB361310A (en) * | 1930-06-18 | 1931-11-18 | Howard Ferguson | Improvements in and relating to motor fuels or like combustible liquids |
US1914509A (en) * | 1931-07-24 | 1933-06-20 | Selden Co | Motor fuel |
GB424205A (en) * | 1932-08-17 | 1935-02-18 | John Westley Orelup | Treatment of oils to improve their colour |
GB447469A (en) * | 1934-07-24 | 1936-05-19 | Wilmot And Cassidy Inc | Improvements in or relating to methods of rendering liquid hydrocarbons fluorescent and dyes therefor |
US2046365A (en) * | 1932-02-24 | 1936-07-07 | Wilmot And Cassidy Inc | Process of testing petroleum hydrocarbons |
US2063575A (en) * | 1934-03-31 | 1936-12-08 | Standard Oil Co | Dispersing of phenolphthalein in mineral lubricating oils |
US2392620A (en) * | 1942-08-20 | 1946-01-08 | Standard Oil Co | Identifying petroleum products |
FR2197886A1 (en) * | 1972-09-05 | 1974-03-29 | Basf Ag | |
FR2230632A1 (en) * | 1973-05-22 | 1974-12-20 | Shin Nisso Kako Co Ltd | |
FR2369099A1 (en) * | 1976-10-26 | 1978-05-26 | Ciba Geigy Ag | MATERIAL FOR SENSITIVE RECORDING |
EP0010740A1 (en) * | 1978-11-03 | 1980-05-14 | BASF Aktiengesellschaft | Spirodipyranes and their use as colour formers in copying processes |
EP0077552A1 (en) * | 1981-10-19 | 1983-04-27 | Matsushita Electric Industrial Co., Ltd. | Colored oil |
-
1987
- 1987-09-18 DE DE19873731458 patent/DE3731458A1/en not_active Withdrawn
-
1988
- 1988-09-09 EP EP88114751A patent/EP0311790A1/en not_active Withdrawn
- 1988-09-15 FI FI884247A patent/FI884247A/en not_active IP Right Cessation
- 1988-09-16 JP JP23018488A patent/JPH01104692A/en active Pending
- 1988-09-16 AU AU22357/88A patent/AU606993B2/en not_active Ceased
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB357179A (en) * | 1930-06-17 | 1931-09-17 | Patent Fuels & Color Corp | Improvements in the art of colouring gasoline or other petroleum distillates |
GB361310A (en) * | 1930-06-18 | 1931-11-18 | Howard Ferguson | Improvements in and relating to motor fuels or like combustible liquids |
US1914509A (en) * | 1931-07-24 | 1933-06-20 | Selden Co | Motor fuel |
US2046365A (en) * | 1932-02-24 | 1936-07-07 | Wilmot And Cassidy Inc | Process of testing petroleum hydrocarbons |
GB424205A (en) * | 1932-08-17 | 1935-02-18 | John Westley Orelup | Treatment of oils to improve their colour |
US2063575A (en) * | 1934-03-31 | 1936-12-08 | Standard Oil Co | Dispersing of phenolphthalein in mineral lubricating oils |
GB447469A (en) * | 1934-07-24 | 1936-05-19 | Wilmot And Cassidy Inc | Improvements in or relating to methods of rendering liquid hydrocarbons fluorescent and dyes therefor |
US2392620A (en) * | 1942-08-20 | 1946-01-08 | Standard Oil Co | Identifying petroleum products |
FR2197886A1 (en) * | 1972-09-05 | 1974-03-29 | Basf Ag | |
FR2230632A1 (en) * | 1973-05-22 | 1974-12-20 | Shin Nisso Kako Co Ltd | |
FR2369099A1 (en) * | 1976-10-26 | 1978-05-26 | Ciba Geigy Ag | MATERIAL FOR SENSITIVE RECORDING |
EP0010740A1 (en) * | 1978-11-03 | 1980-05-14 | BASF Aktiengesellschaft | Spirodipyranes and their use as colour formers in copying processes |
EP0077552A1 (en) * | 1981-10-19 | 1983-04-27 | Matsushita Electric Industrial Co., Ltd. | Colored oil |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0438734A1 (en) * | 1990-01-22 | 1991-07-31 | BASF Aktiengesellschaft | Marked mineral oils and process to mark mineral oils by means of basic dyes |
US5145573A (en) * | 1990-01-22 | 1992-09-08 | Basf Aktiengesellschaft | Marked mineral oils and method of marking mineral oils with basic dyes |
EP0490232A1 (en) * | 1990-12-14 | 1992-06-17 | BASF Aktiengesellschaft | Device for detecting marked mineral oils |
US5882358A (en) * | 1995-06-07 | 1999-03-16 | United Color Manufacturing, Inc. | Colored transmission fluid |
EP1001003A1 (en) * | 1998-11-09 | 2000-05-17 | Morton International, Inc. | Method for invisibly tagging petroleum products using visible dyes |
WO2000059751A1 (en) * | 1999-04-06 | 2000-10-12 | Imperial Chemical Industries Plc | Reservoir combination for flammable fluids |
WO2003078551A2 (en) * | 2002-03-15 | 2003-09-25 | Shell Internationale Research Maatschappij B.V. | Oil composition and method of detecting a marker in an oil composition |
WO2003078551A3 (en) * | 2002-03-15 | 2004-01-15 | Shell Int Research | Oil composition and method of detecting a marker in an oil composition |
Also Published As
Publication number | Publication date |
---|---|
DE3731458A1 (en) | 1989-03-30 |
JPH01104692A (en) | 1989-04-21 |
AU606993B2 (en) | 1991-02-21 |
AU2235788A (en) | 1989-03-23 |
FI884247A (en) | 1989-03-19 |
FI884247A0 (en) | 1988-09-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1671545C2 (en) | Pressure sensitive copier paper | |
DE1809778B2 (en) | COLOR IMAGES FOR PRESSURE SENSITIVE REPRODUCTION PAPER AND THE PROCESS FOR THE PRODUCTION | |
DE2323803B2 (en) | Spirodipyrans and their use as color formers for copying processes | |
EP0256460A2 (en) | Dye mixtures | |
DE2614944A1 (en) | CHROMOGENIC COMPOUNDS | |
DE2307774B2 (en) | THERMO-SENSITIVE TWO-COLOR RECORDING PAPER | |
EP0311790A1 (en) | Marked mineral oil product, and process to mark mineral oil products | |
DE2163658A1 (en) | Pressure sensitive copier paper | |
DE855406C (en) | Process for making records | |
DE1421395A1 (en) | Coatings and impression processes using phenols and colored products thereof | |
DE3116815C2 (en) | ||
DE2556083A1 (en) | PRESSURE SENSITIVE RECORDING MATERIAL | |
DE1561748C3 (en) | Recording material | |
DE2259409A1 (en) | CHROMOGENIC COMPOUND | |
DE3507173A1 (en) | COLOR IMAGE MIXTURES AND PRESSURE SENSITIVE RECORD MATERIAL CONTAINING THESE MIXTURES | |
DE2753816B2 (en) | Solvent mixture and its use in copier papers | |
DE2430568C3 (en) | Spirodipyrans and their use as color formers for pressure-sensitive recording materials | |
DE2640196C2 (en) | Dye solvent preparations for pressure sensitive copier systems | |
DE2314540A1 (en) | CHROMOGENIC BENZOPYRANE COMPOUNDS | |
EP0716743B1 (en) | Method of detecting naphthylamines in mineral oils | |
DE2230225C2 (en) | New quinoxaline spiropyrans and their use as color formers for copying processes | |
DE2509793C2 (en) | Diazarhodamine lactones and their use as color formers for copy processes | |
DE69310114T2 (en) | Solvents containing diisopropylbiphenyl and triisopropylbiphenyl for use in carbonless paper and products using the same | |
DE4010641C2 (en) | Color former mixture for pressure and heat sensitive recording systems | |
DE2702017A1 (en) | PRESSURE-SENSITIVE TRANSPARENCY PAPER |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE FR GB IT |
|
17P | Request for examination filed |
Effective date: 19890331 |
|
17Q | First examination report despatched |
Effective date: 19900326 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN |
|
18W | Application withdrawn |
Withdrawal date: 19910316 |
|
R18W | Application withdrawn (corrected) |
Effective date: 19910316 |