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The inventive technology may involve, in particular embodiments, novel use of a non-porous, high surface energy stationary phase to adsorb, in reversible fashion, the most polar component of a resins fraction of an input hydrocarbon when a mobile phase is passed over the stationary phase. Such rever

The inventive technology may involve, in particular embodiments, novel use of a non-porous, high surface energy stationary phase to adsorb, in reversible fashion, the most polar component of a resins fraction of an input hydrocarbon when a mobile phase is passed over the stationary phase. Such reversible adsorption prevents irreversibly adsorption of such components on active stationary phase(s) downflow of the non-porous, high surface energy stationary phase, thereby conserving stationary phase costs and increasing resolution of resins elutions, and accuracy of hydrocarbon component results. Aspects of the inventive technology may also involve a novel combination of a solubility based asphaltene component fractionating and analysis method and an adsorption chromatography method for separating and/or analyzing saturate, aromatics and resins components of an input hydrocarbon.

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1. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample, said method comprising the steps of: entraining said first hydrocarbon sample into and as part of a first run amount of a first solvent mobile phase, said first solvent mobil

1. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample, said method comprising the steps of: entraining said first hydrocarbon sample into and as part of a first run amount of a first solvent mobile phase, said first solvent mobile phase having a first solvent strength;passing said first run amount of said first solvent mobile phase over a particular bulk quantity of a non-porous, high surface energy stationary phase;reversibly adsorbing resins materials of said first hydrocarbon sample onto said particular bulk quantity of said non-porous, high surface energy stationary phase;passing said first run amount of said first solvent mobile phase over a particular bulk quantity of an active stationary phase;eluting a saturates component of said first hydrocarbon sample;passing a first run amount of a second solvent mobile phase over said particular bulk quantity of said active stationary phase, said second solvent mobile phase having a second solvent strength that is greater than said first solvent strength;eluting an aromatic component of said first hydrocarbon sample;passing a first run amount of a third solvent mobile phase over said particular bulk quantity of said non-porous, high surface energy stationary phase, said third solvent mobile phase having a third solvent strength that is greater than said second solvent strength;eluting a resins component of said first hydrocarbon sample;entraining said second, different hydrocarbon sample into and as part of a second run amount of said first solvent mobile phase;passing said second run amount of said first solvent mobile phase over said particular bulk quantity of said non-porous, high surface energy stationary phase;reversibly adsorbing resins materials of said second, different hydrocarbon sample onto said particular bulk quantity of said non-porous, high surface energy stationary phase;passing said second run amount of said first solvent mobile phase over said particular bulk quantity of said active stationary phase;eluting a saturates component of said second, different hydrocarbon sample;passing a second run amount of said second solvent mobile phase over said particular bulk quantity of said active stationary phase;eluting an aromatic component of said second, different hydrocarbon sample;passing a second run amount of said third solvent mobile phase over said particular bulk quantity of said non-porous, high surface energy stationary phase; andeluting a resins component of said second, different hydrocarbon sample. 2. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 wherein said method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample is a method of successively eluting components of a first crude oil sample and then a second, different crude oil sample. 3. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 wherein said method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample is a method of successively eluting components of a first heavy oil sample and then a second, different heavy oil sample. 4. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 wherein said method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample is a method of successively eluting components of a first opportunity crude oil sample and then a second, different opportunity crude oil sample. 5. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 wherein said method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample is a method of successively eluting components of a first maltenes sample generated from a first oil and then a second, different maltenes sample generated from a second oil. 6. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 further comprising the steps of reversibly adsorbing highly aromatic materials of said first and second, different hydrocarbon samples. 7. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 further comprising the steps of analyzing said saturates, aromatics and resins components of said first and second, different hydrocarbon samples to generate analysis results. 8. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 further comprising the step of solvent flushing said particular bulk quantity of said non-porous, high surface energy stationary phase and said particular bulk quantity of said active stationary phase after performing said step of eluting a resins component of said first hydrocarbon sample but before performing said step of entraining said second, different hydrocarbon sample of a hydrocarbon into and as part of a second run amount of said first solvent mobile phase. 9. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 wherein said step of entraining said first hydrocarbon sample into and as part of a first run amount of a first solvent mobile phase comprises the step of entraining said first hydrocarbon sample into and as part of a first run amount of a mobile phase that comprises a solvent selected from the group consisting of: pentane, hexane, heptane, iso-octane, and trimethylpentane. 10. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 wherein said step of passing said first run amount of said first solvent mobile phase over a particular bulk quantity of a non-porous, high surface energy stationary phase comprises the step of passing said first run amount of said first solvent mobile phase over a particular bulk quantity of a stationary phase that comprises a medium selected from the group consisting of: glass, ceramics and metal. 11. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 wherein said step of passing said first run amount of said first solvent mobile phase over a particular bulk quantity of an active stationary phase comprises the step of passing said first run amount of said first solvent mobile phase over a particular bulk quantity of a stationary phase that comprises a medium selected from the group consisting of: activity enhanced silica and activity enhanced alumina. 12. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 wherein said step of passing a first run amount of a second solvent mobile phase over a particular bulk quantity of an active stationary phase comprises the step of passing a first run amount of a toluene over a particular bulk quantity of an active stationary phase. 13. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 wherein said step of passing a first run amount of a third solvent mobile phase over said particular bulk quantity of said non-porous, high surface energy stationary phase comprises the step of passing a first run amount of methylene chloride:methanol over said particular bulk quantity of said non-porous, high surface energy stationary phase. 14. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 further comprising the step of passing said first run amount of said first solvent mobile phase over a particular bulk quantity of less active stationary phase that is distinct from said particular bulk quantities of said non-porous, high surface energy stationary phase and said active stationary phase, wherein said less active stationary phase is less active than said non-porous, high surface energy stationary phase and said active stationary phase. 15. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 further comprising the step of passing said first run amount of said first solvent mobile phase over a particular bulk quantity of an inert stationary phase. 16. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 15 wherein said inert stationary phase comprises polytetrafluoroethylene. 17. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 15 further comprising the step of precipitating asphaltenes of said first hydrocarbon sample within said inert stationary phase. 18. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 15 further comprising the step of passing at least one asphaltene solvent over said particular bulk quantity of said inert stationary phase. 19. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 18 further comprising the step of eluting an asphaltene component of said first hydrocarbon sample. 20. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 18 further comprising the step of passing said second run amount of said first solvent mobile phase over said particular bulk quantity of an inert stationary phase. 21. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 20 further comprising the step of precipitating asphaltenes of said second, different hydrocarbon sample within said inert stationary phase. 22. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 20 further comprising the step of passing at least one asphaltene solvent over said particular bulk quantity of said inert stationary phase. 23. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 22 further comprising the step of eluting an asphaltene component of said second, different hydrocarbon sample. 24. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 15 further comprising the step of passing said second run amount of said first solvent mobile phase over said particular bulk quantity of said inert stationary phase. 25. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 7 further comprising the step of using said analysis results to improve a process selected from the group consisting of coking onset estimation, oil processing, oil fractionating, oil production, pipeline fouling mitigation, hydrotreating, distillation, vacuum distillation, atmospheric distillation, visbreaking, blending, asphalt formation, asphalt extraction, and asphaltene content of oil measurement. 26. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 7 further comprising the step of using said analysis results to further a processing related goal selected from the group consisting of: increasing distillate yield and quality; displacing high-sulfur fuel oil; boosting propylene output; mitigating fouling and corrosion; and reducing carbon footprint. 27. A method of successively eluting components of a first hydrocarbon sample and then a second, different hydrocarbon sample as described in claim 1 further comprising the step of adding at least one additional material into and as part of at least one of said first run amount of said first solvent mobile phase and said second run amount of said first solvent mobile phase, wherein said additional material is selected from the group consisting of additive and rejuvenator.