1. A method comprising the steps of:
providing a vessel having a substantially chemically inert stationary phase established therein and having at least one vessel inlet;
inputting a precipitant solvent into said vessel through at least one vessel inlet;
inputting a solution into said vessel through at least one vessel inlet;
intentionally precipitating asphaltenes within said vessel and in the presence of said substantially chemically inert stationary phase, wherein said substantially chemically inert stationary phase is substantially chemically inert relative to said asphaltenes;
generating a remnant liquid upon performing said step of intentionally precipitating said asphaltenes;
inputting a material dissolving solvent into said vessel through at least one vessel inlet; and
dissolving at least a portion of said asphaltenes with said material dissolving solvent to generate a dissolved material solution.
2. A method as described in claim 1 wherein said step of inputting a solution into said vessel through at least one vessel inlet comprises the step of inputting a sample into said vessel.
3. A method as described in claim 2 wherein said step of inputting a sample into said vessel through at least one vessel inlet comprises the step of inputting oil into said vessel.
4. A method as described in claim 2 wherein said step of inputting a sample into said vessel through at least one vessel inlet comprises the step of inputting a wax component of oil into said vessel.
5. A method as described in claim 2 wherein said step of inputting a sample into said vessel through at least one vessel inlet comprises the step of inputting an asphaltene into said vessel.
6. A method as described in claim 2 wherein said step of inputting a solution into said vessel through at least one vessel inlet further comprises the step of inputting a sample solvent into said vessel.
7. A method as described in claim 2 wherein said substantially chemically inert stationary phase is also substantially chemically inert relative to said sample.
8. A method as described in claim 1 wherein said step of inputting a solution into said vessel through at least one vessel inlet comprises the step of inputting oil into said vessel.
9. A method as described in claim 1 wherein said step of inputting a precipitant solvent into said vessel through at least one vessel inlet comprises the step of inputting into said vessel a precipitant solvent selected from the group consisting of low polarity solvents, low polarity solvent mixtures, aliphatic solvents, heptane, pentane and isooctane.
10. A method as described in claim 1 wherein said step of generating a remnant liquid comprises the step of generating a remnant solution.
11. A method as described in claim 2 further comprising the step of determining at least one characteristic of said sample.
12. A method as described in claim 11 wherein said step of determining at least one characteristic of said sample comprises the step of using a technique selected from the group consisting of evaporative light scattering, mass spectrometry, optical absorbance, x-ray, conductivity, oxidationreduction, refractive index, polarimetry, atomic spectroscopy, and fluorescence.
13. A method as described in claim 11 wherein said step of determining at least one characteristic of said sample comprises the step of analyzing said remnant liquid.
14. A method as described in claim 11 wherein said step of determining at least one characteristic of said sample comprises the step of determining a weight percentage of asphaltenes.
15. A method as described in claim 11 wherein said step of determining at least one characteristic of said sample comprises the step of analyzing said dissolved material solution.
16. A method as described in claim 11 wherein said step of determining at least one characteristic of said sample comprises the step of determining a mass fraction of heptane asphaltenes soluble in cyclohexane.
17. A method as described in claim 11 wherein said step of determining at least one characteristic of said sample comprises the step of determining at least two characteristics of said sample.
18. A method as described in claim 17 wherein said step of determining at least two characteristics of said sample comprises the step of determining a cyclohexane soluble peak value and a methylene chloride soluble peak value.
19. A method as described in claim 1 wherein said step of inputting a material dissolving solvent comprises the step of inputting a material dissolving solvent selected from the group consisting of solvents having a higher polarity than that of said precipitant solvent, solvent mixtures having a higher polarity than that of said precipitant solvent, naphthenic oils, aromatic oils, ketones, halogenated solvents, cyclohexane, toluene, cyclohexanone, and methylene chloride.
20. A method as described in claim 1 further comprising the step of separating said remnant liquid from said asphaltenes.
21. A method as described in claim 1 further comprising the step of removing said remnant liquid from said vessel.
22. A method as described in claim 20 further comprising the step of replacing said remnant liquid with said material dissolving solvent.
23. A method as described in claim 1 further comprising the step of eluting said dissolved material solution from said vessel.
24. A method as described in claim 1 wherein said step of inputting a material dissolving solvent into said vessel comprises the step of inputting cyclohexane, or a different solvent or solvent mixture with substantially the same polarity as cyclohexane.
25. A method as described in claim 1 wherein said step of dissolving at least a portion of said asphaltenes with said material dissolving solvent comprises the step of dissolving only a first portion of said asphaltenes with said material dissolving solvent.
26. A method as described in claim 25 further comprising the step of inputting a second material dissolving solvent into said vessel through at least one vessel inlet to dissolve at least a second portion of said asphaltenes.
27. A method as described in claim 26 wherein said step of inputting a second material dissolving solvent into said vessel comprises the step of inputting a stronger material dissolving solvent.
28. A method as described in claim 27 wherein said step of inputting a stronger material dissolving solvent into said vessel comprises the step of inputting into said vessel solvent that gradually increases in strength.
29. A method as described in claim 28 wherein said step of inputting into said vessel solvent that gradually increases in strength is performed during continuous solvent flow.
30. A method as described in claim 27 wherein said strengths of said material dissolving solvents do not change in a step gradient fashion.
31. A method as described in claim 27 wherein said strengths of said material dissolving solvents change in a step gradient fashion.
32. A method as described in claim 25 further comprising the step of inputting increasingly stronger material dissolving solvent into said vessel to dissolve at least a second portion of said asphaltenes and generate a second dissolved material solution.
33. A method as described in claim 32 wherein said step of inputting increasingly stronger material dissolving solvent comprises the step of inputting material dissolving solvent that gradually increases in strength.
34. A method as described in claim 33 wherein said step of step of inputting material dissolving solvent that gradually increases in strength is performed during continuous solvent flow.
35. A method as described in claim 32 where input solvent strengths do not change in a step gradient fashion.
36. A method as described in claim 26 further comprising the step of replacing said dissolved material solution with said second material dissolving solvent.
37. A method as described in claim 26 wherein said step of inputting a second material dissolving solvent into said vessel comprises the step of inputting toluene, or a different solvent or solvent mixture with substantially the same polarity as toluene.
38. A method as described in claim 32 further comprising the steps of analyzing said second dissolved material solution.
39. A method as described in claim 32 wherein said step of inputting increasingly stronger material dissolving solvent into said vessel to dissolve at least a second portion of said asphaltenes comprises the step of inputting increasingly stronger material dissolving solvent into said vessel to dissolve said second and at least a third portion of said asphaltenes.
40. A method as described in claim 39 further comprising the step of generating a third dissolved material solution.
41. A method as described in claim 39 wherein said step of inputting increasingly stronger material dissolving solvent into said vessel comprises the step of inputting methylene chloride or a solvent or solvent mixture with substantially the same polarity as methylene chloride.
42. A method as described in claim 40 further comprising the step of analyzing said third dissolved material solution.
43. A method as described in claim 1 further comprising the step of fractionating said solution into at least two parts.
44. A method as described in claim 1 wherein each of said steps is started in the order in which it appears.
45. A method as described in claim 1 wherein said step of providing a vessel having a substantially chemically inert stationary phase established therein comprises the step of providing a vessel having established therein a stationary phase selected from the group of: oligomers of PTFE, polymers of PTFE, polyphenylene sulfide, fluorinated polymers, silicon polymer and PEEK.
46. A method as described in claim 1 wherein said step of providing a vessel having a substantially chemically inert stationary phase established therein comprises the step of providing a column having a substantially chemically inert stationary phase established therein.
47. A method as described in claim 46 wherein said step of providing a column comprises the step of providing a column that is part of a chromatograph.
48. A method as described in claim 1 wherein said step of providing a vessel having a substantially chemically inert stationary phase established therein comprises the step of providing a batch type vessel having a substantially chemically inert stationary phase established therein.
49. A method as described in claim 1 wherein said step of intentionally precipitating asphaltenes within said vessel comprises the step of intentionally precipitating solid material.
50. A method as described in claim 1 wherein said step of intentionally precipitating a asphaltenes within said vessel comprises the step of intentionally precipitating gel or viscous liquid.
51. A method as described in claim 1 wherein said method is accomplished, at least in part, with a flow system.
52. A method as described in claim 51 wherein said flow system is a continuous flow system.
53. A method as described in claim 1 wherein said step of inputting a precipitant solvent into said vessel through at least one vessel inlet comprises the step of inputting a liquid into said vessel through at least one vessel inlet.
54. A method as described in claim 1 wherein said step of inputting a precipitant solvent into said vessel through at least one vessel inlet comprises the step of inputting gel or viscous liquid.
55. A method as described in claim 1 wherein said method is a method selected from the group consisting of coking onset estimation method, oil processing method; oil fractionating method, oil production method, pipeline fouling related method, hydrotreating, distillation method, vacuum distillation method, atmospheric distillation method, visbreaking method, blending method, asphalt formation method, asphalt extraction method, and asphaltene content of oil measurement method.
56. A method as described in claim 1 wherein said method is an automated method.
The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.
What is claimed is:
1. An isolated nucleic acid molecule comprising a STP2 sequence polymorphism, as part of other than a naturally occurring chromosome.
2. A nucleic acid probe for detection of STP2 locus polymorphisms, comprising a polymorphic sequence listed in Table 4.
3. A nucleic acid probe according to claim 2, wherein said probe is conjugated to a detectable marker.
4. An array of oligonucleotides comprising:
two or more probes for detection of STP2 locus polymorphisms, said probes comprising at least one form of a polymorphic sequence listed in Table 4.
5. A method for detecting in an individual a polymorphism in STP2 metabolism of a substrate, the method comprising:
analyzing the genome of said individual for the presence of at least one STP2 polymorphism listed in Table 4; wherein the presence of said predisposing polymorphism is indicative of an alteration in STP2 expression or activity.
6. A method according to claim 5, wherein said analyzing step comprises detection of specific binding between the genomic DNA of said individual with an array of oligonucleotides comprising:
two or more probes for detection of STP2 locus polymorphisms, said probes comprising at least one form of a polymorphic sequence listed in Table 4.
7. A method according to claim 5, wherein said alteration in STP2 expression is tissue specific.
8. A method according to claim 5, wherein said alteration in STP2 expression is in response to a STP2 modifier.
9. A method according to claim 8, wherein said modifier induces STP2 expression.
10. A method according to claim 8, wherein said modifier inhibits STP2 expression.