Method for evaluating the remaining useful life of a hydrocarbon oil

• US 4,764,258 A
• Filed: 12/23/1986
• Issued: 08/16/1988
• Est. Priority Date: 12/23/1986
• Status: Expired due to Term

• Current Assignee: University of Dayton
• Original Assignee: University of Dayton
• Inventors: Kauffman, Robert E.
• Primary Examiner(s): Kaplan, G. L.
• Application Number:
  US06/945,603
• Time in Patent Office: 602 Days
• Field of Search: 436/60, 436/61, 204/1 T
• US Class Current: 205/786
• CPC Class Codes: G01N 33/2888 Lubricating oil characteristics, e.g. deterioration lubricating properties G01N33/30

Abstract

A method is disclosed for measuring the remaining useful life of a hydrocarbon oil containing at least one additive species. An oil sample is mixed with a solvent, a solid substrate, and in some cases an electrolyte to produce an analysis sample. The analysis sample is placed into an electrolytic cell and subjected to a voltammetric analysis, whereby increasing potential is applied to the cell to produce an oxidation reaction and a varying electric current. The current during the voltammetric analysis is measured and recorded. Remaining useful life for the oil is then determined from the oxidation current wave height produced.

Claims

1. A method for measuring the remaining useful life of a hydrocarbon oil containing an oil basestock and at least one additive species, comprising the steps of:

mixing an oil sample with a solvent and a solid substrate to produce an analysis sample wherein said basestock coats said substrate;

permitting said substrate and said basestock coated thereon to settle from said analysis sample;

placing said analysis sample into an electrolytic cell;

applying an electric potential of a first value to said analysis sample to produce an electric current therethrough;

varying said potential from said first value to a second value to produce an oxidation reaction of said additive species within said cell; and

measuring and recording said current during said oxidation reaction.

2. The method as defined in claim 1, wherein said additive species is a substituted phenol antioxidant or an oxidation product of the substituted phenol with antioxidant capacity.

3. The method as defined in claim 2, wherein said solvent is ethanol having an inorganic base added thereto.

4. The method as defined in claim 3, wherein said inorganic base is potasssium hydroxide (KOH).

5. The method as defined in claim 4, wherein said potassium hydroxide is added to said ethanol in an amount of 50 to 100 millimoles per liter of ethanol.

6. The method as defined in claim 2, wherein said solid substrate is sand.

7. The method as defined in claim 6, wherein said sand is added in an amount of at least 2.0 g of sand to 1.0 ml of said oil.

8. The method as defined in claim 2, wherein said first and second potential values are within the range of -1.5 V and +1.5 V.

9. The method as defined in claim 8, wherein said first and second potential values are, respectively, -0.2 V and +0.2 V.

10. The method as defined in claim 9, wherein said potential is varied at a rate of 0.01 V/sec to 30.0 V/sec.

11. The method as defined in claim 9, wherein said potential is varied at a rate of 1.0 V/sec.

12. The method as defined in claim 1, wherein said additive species is a metal-dithiodiphosphate multi-function additive or an oxidation product of the metal-dithiodiphosphate with antioxidant capacity.

13. The method as defined in claim 12, comprising the step of mixing an electrolyte into said analysis sample.

14. The method as defined in claim 13, wherein said solvent contains up to 1 part distilled water per 5 parts of acetone.

15. The method as defined in claim 13, wherein said solvent contains 1 part distilled water per 10 parts of acetone.

16. The method as defined in claim 15, wherein said electrolyte is lithium perchlorate (LiClO₄).

17. The method as defined in claim 16, wherein said lithium perchlorate is added to the 1:

10 water/acetone solution in an amount of 50 to 100 millimoles per liter of solution.

18. The method as defined in claim 12, wherein said solid substrate is sand.

19. The method as defined in claim 12, wherein said substrate is added in an amount of at least 2.0 g substrate to 1.0 ml of said oil.

20. The method as defined in claim 12, wherein said first and second potential values are within the range of -1.5 V and +1.5 V.

21. The method as defined in claim 20, wherein said first and second potential values are, respectively, -0.2 V and +0.9 V.

22. The method as defined in claim 21, wherein said potential is varied at a rate of 0.01 V/sec of 30.0 V/sec.

23. The method as defined in claim 21 wherein said potential is varied at a rate of 1.0 V/sec.

24. The method as defined in claim 1, wherein said electrolytic cell includes a microelectrode, a reference electrode, and an auxiliary electrode.

25. The method as defined in claim 24, wherein said microelectrode is a glassy carbon electrode.

26. Tne method as defined in claim 24, wherein said reference electrode is Ag/AgCl.

27. The method as defined in claim 24, wherein said auxiliary electrode is platinum wire.

28. The method as defined in claim 1, comprising the further step of determining the maximum current produced during said oxidation reaction.

29. A method for measuring the remaining useful life of a hydrocarbon oil containing an oil basestock and at least one substituted phenol antioxidant species or an oxidation product of a substituted phenol with antioxidant capacity, comprising the steps of:

mixing an oil sample with a solvent, an inorganic base and a solid substrate to produce an analysis sample wherein said basestock coats said substrate;

permitting said substrate and said basestock coated thereon to settle from said analysis sample;

placing said analysis sample into an electrolytic cell;

subjecting said analysis sample to a voltammetric analysis, whereby a varying electric current is produced during an oxidation reaction within said cell; and

measuring and recording said current during said voltammetric analysis.

30. The method as defined in claim 29, comprising the further step of determining a maximum current value during said voltammetric analysis.

31. The method as defined in claim 29, comprising the further step of determining a maximum current value during said voltammetric analysis.

32. A method for measuring the remaining useful life of a hydrocarbon oil containing an oil basestock and at least one metal dithiodiphosphate multi-function species or an oxidation product of a metal dithiodiphosphate with antioxidant capacity, comprising the steps of:

mixing an oil sample with a solvent, an electrolyte and a solid substrate to produce an analysis sample wherein said basestock coats said substrate;

permitting said substrate and said basestock coated thereon to settle from said analysis sample;

placing said analysis sample into an electrolytic cell;

subjecting said analysis sample to a voltammetric analysis, whereby a varying electric current is produced during an oxidation reaction within said cell; and

meausring and recording said current during said voltammetric analysis.