Claims
- 1. A method of authenticating a bulk liquid, which consists of introducing into said bulk liquid a chemiluminescent marker substance capable of taking part in a chemiluminescent reaction, withdrawing a sample of said bulk liquid to be authenticated, exposing said sample to conditions required to trigger a chemiluminescence reaction, determining whether a chemilumninescence reaction occurs, and authenticating said bulk liquid based on whether said chemiluminescence reaction occurs.
- 2. A method according to claim 1, wherein said bulk liquid is a mineral oil based product.
- 3. A method according to claim 1, wherein said chemiluminescent marker substance is substantially insoluble in water.
- 4. A method according to claim 1, wherein said chemiluminescent marker substance is present in said bulk liquid in an amount between 0.001 ng/.mu.l and 10 ng/.mu.l.
- 5. A method according to claim 1, wherein the chemiluminescent marker substance is immunologically unbound in said bulk liquid.
- 6. A method according to claim 1, wherein said chemiluminescent marker substance is an acridinium compound capable of undergoing a chemiluminescent reaction and of the general formula: ##STR3## wherein R.sub.1 is a moiety capable of being part of a quaternary nitrogen center selected from the group consisting of alkl, alkenyl, alkynyl, alkoxyl or aryl containing groups,
- R.sub.2 and R.sub.3 may be the same as R.sub.1 or a hydroxyl, carboxyl, amino, substituted amino, or halide group,
- R.sub.4 is a moiety whose chemical reactivity permits the compound to undergo chemilumnescent reaction selected from the group consisting of: ##STR4## and X.sup.- is an anion.
- 7. A method according to claim 2, wherein said bulk liquid is selected from the group consisting of petroleum, diesel oil and lubricating oils.
- 8. A method of detecting subsequent dilution of a sample of bulk liquid which consists of introducing into an undiluted bulk liquid a known amount of a chemiluminescent marker substance, withdrawing a sample of said bulk liquid, initiating a chemiluminescent reaction in said sample, determining characteristics of said reaction, and comparing the characteristics of said reaction with those of a chemiluminescent reaction in the undiluted bulk liquid to determine the extent of dilution of said bulk liquid.
- 9. A method according to claim 8, wherein said bulk liquid is selected from the group consisting of petroleum, diesel oil, and lubricating oils.
- 10. A method according to claim 8, wherein said chemiluminescent marker substance is an acridinium compound capable of undergoing a chemiluminescent reaction and of the general formula: ##STR5## wherein R.sub.1 is a moiety capable of being part of a quaternary nitrogen center selected from the group consisting of alky, alkenyl, alkynyl, alkoxyl or aryl containing groups,
- R.sub.2 and R.sub.3 may be the same as R.sub.1 or a hydroxyl, carboxyl, amino, substituted amino, or halide group,
- R.sub.4 is a moiety whose chemical reactivity permits the compound to undergo chemiluminescent reaction selected from the group consisting of: ##STR6## and X.sup.- is an anion.
- 11. A method of analyzing a bulk liquid to determine the presence or quantity of an additive present in the bulk liquid, said bulk liquid including a predetermined amount of a chemiluminescent marker substance indicating the presence of, or related to the quantity of, said additive, which method consists of withdrawing a sample of said bulk liquid to be identified or analyzed, initiating the chemiluminescent reaction in said sample and observing the characteristics of said reaction to determine the presence or the quantity of said additive.
- 12. A method according to claim 11, wherein said bulk liquid is selected from the group consisting of petroleum, diesel oil, and lubricating oils.
- 13. A method according to claim 11, wherein said chemiluminescent marker substance is an acridinium compound capable of undergoing a chemiluminescent reaction and of the general formula: ##STR7## wherein R.sub.1 is a moiety capable of being part of a quaternary nitrogen center selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxyl or aryl containing groups,
- R.sub.2 and R.sub.3 may be the same as R.sub.1 or a hydroxyl, carboxyl, amino, substituted amino, or halide group,
- R.sub.4 is a moiety whose chemical reactivity permits the compound to undergo chemiluminescent reaction selected from the group consisting of: ##STR8## and X.sup.- is an anion.
Priority Claims (1)
Number |
Date |
Country |
Kind |
9315129.8 |
Jul 1993 |
GBX |
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Parent Case Info
This is a continuation of application Ser. No. 08/277,864 filed on Jul. 20, 1994, now abandoned.
US Referenced Citations (5)
Foreign Referenced Citations (2)
Number |
Date |
Country |
0327163 |
Aug 1989 |
EPX |
0512404A1 |
Nov 1992 |
EPX |
Non-Patent Literature Citations (2)
Entry |
Fleschka et al. Quantitative Analytical Chemistry, 2nd Edition, p. 478, 1982. |
Sax et al. Hawley's Condensed Chemical Dictionary, 11th Edition, p. 17, 1987. |
Continuations (1)
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Number |
Date |
Country |
Parent |
277864 |
Jul 1994 |
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