Method of improving the accuracy when quantifying fluorescence markers in fuels

1. A method of quantification of an analyte in a hydrocarbon, the analyte comprising a marking compound, the method comprising:

obtaining a first sample comprising (a) the hydrocarbon and (b) the marking compound;

obtaining a homogeneity inducing material operable to increase the homogeneity of the first sample;

contacting the homogeneity inducing material with an aliquot of the first sample in a volumetric ratio of greater than or equal to about 5:1 to produce a second sample; and

determining an amount of the marking compound in the second sample using an analytical technique.

2. The method of claim 1 further comprising determining whether the first sample is adulterated based on a comparison of an amount of the marking compound in the first sample to a reference standard having a known amount of the marking compound.

3. The method of claim 1 , wherein the analytical technique comprises fluorescence spectroscopy, gas chromatography, mass spectrometry, ultraviolet spectroscopy, high-pressure liquid chromatography, infrared spectroscopy, or a combination thereof.

4. The method of claim 1 , wherein the hydrocarbon comprises gasoline, diesel fuel, biodiesel fuel, kerosene, liquefied petroleum gas, ethanol, or a combination thereof.

5. The method of claim 1 , wherein the marking compound comprises an organic compound having a fluorescence in a wavelength range of from about 600 nm to about 800 nm.

6. The method of claim 5 , wherein the marking compound comprises a phthalocyanine, a violanthrone, an azadipyrromethene, naphthalocyanine, rhodamine, oxazine, coumarin, a cyanine fluorophore, or a combination thereof.

7. The method of claim 1 , wherein the marking compound is not resistant to solvatochromic shifting.

8. The method of claim 1 , wherein the marking compound is present in an amount of from about 1 ppb to about 1000 ppb.

9. The method of claim 1 , wherein the homogeneity inducing material comprises one or more aliphatic hydrocarbons, aromatic hydrocarbons, petroleum distillates, halogenated aliphatic hydrocarbons, halogenated aromatic hydrocarbons, or a combination thereof.

10. The method of claim 1 further comprising determining whether the first sample is adulterated based on a comparison of an amount of the marking compound in the first sample to a reference standard having a known amount of the marking compound;

wherein the analytical technique comprises fluorescence spectroscopy, gas chromatography, mass spectrometry, ultraviolet spectroscopy, high-pressure liquid chromatography, infrared spectroscopy, or a combination thereof; and

wherein the hydrocarbon comprises gasoline, diesel fuel, biodiesel fuel, kerosene, liquefied petroleum gas, ethanol, or a combination thereof.

11. The method of claim 10 , wherein the marking compound (i) comprises an organic compound having a fluorescence in a wavelength range of from about 600 nm to about 800 nm, (ii) comprises a phthalocyanine, a violanthrone, an azadipyrromethene, naphthalocyanine, rhodamine, oxazine, coumarin, a cyanine fluorophore, or a combination thereof, or (iii) is not resistant to solvatochromic shifting; and

wherein the homogeneity inducing material comprises one or more aliphatic hydrocarbons, aromatic hydrocarbons, petroleum distillates, halogenated aliphatic hydrocarbons, halogenated aromatic hydrocarbons, or a combination thereof.

12. A method comprising:

obtaining a first sample comprising (a) a hydrocarbon, (b) a marking compound, and (c) a homogeneity-varying material that reduces a signal intensity of the marking compound measured by a first of at least two differing and independent analytical techniques, wherein the first sample has a degree of homogeneity in a range of from about 0.1 to about 0.4;

contacting a matrix comprising one or more aliphatic hydrocarbons, aromatic hydrocarbons petroleum distillates, halogenated aliphatic hydrocarbons, halogenated aromatic hydrocarbons, or a combination thereof with an aliquot of the first sample in a volumetric ratio of greater than or equal to about 5:1 to produce a second sample, wherein the second sample has a degree of homogeneity in a range of from about 0.8 to about 0.95;

determining an amount of the marking compound in the first sample using a first of the least two differing and independent analytical techniques; and

determining an amount of the marking compound in the second sample using a second of the least two differing and independent analytical techniques,

wherein an agreement between amount of the marking compound determined by the first of the at least two differing and independent analytical techniques and the amount of the marking compound determined by the second of the at least two differing and independent analytical techniques is increased relative to a same method absent the matrix.

13. The method of claim 12 , wherein the homogeneity-varying material comprises one or more refined fuel products, biofuels, fuel additives, oxygenates, common fuel adulterants, or a combination thereof.

14. The method of claim 12 further comprising determining whether the first sample is adulterated based on a comparison of an amount of the marking compound in the first sample to a reference standard having a known amount of the marking compound.

15. The method of claim 12 , wherein the agreement between the at least two differing and independent analytical techniques is increased by at least 5%, relative to a same method absent the matrix.

16. A method comprising:

A obtaining a fuel comprising (a) a fluorescent marking compound and (b) a signal-dampening material which reduces readings obtained via a first of at least two differing and independent analytical techniques, wherein the fuel has a degree of homogeneity in a range of from about 0.1 to about 0.2;

contacting a matrix comprising one or more aliphatic hydrocarbons, aromatic hydrocarbons, petroleum distillates, halogenated aliphatic hydrocarbons, halogenated aromatic hydrocarbons, or a combination thereof with an aliquot of the fuel in a volumetric ratio of greater than or equal to about 5:1 to produce a sample, wherein the sample has a degree of homogeneity of greater than or equal to about 0.8;

determining an amount of the fluorescent marking compound in the sample using the first of the at least two differing and independent analytical techniques; and

determining an amount of the fluorescent marking compound in another aliquot of the fuel using a second of the least two differing and independent analytical techniques,

wherein an agreement between the amount of the fluorescent marking compound determined by the first of the at least two differing and independent analytical techniques and the amount of the fluorescent marking compound determined by the second of the at least two differing and independent analytical techniques is increased relative to a same method absent the matrix.

17. The method of claim 16 , wherein the at least two differing and independent analytical techniques comprise fluorescence spectroscopy and gas chromatography-mass spectrometry.

18. The method of claim 16 further comprising determining an amount of the fluorescent marking compound in the fuel from the amount of the fluorescent marking compound determined by the first of the at least two differing and independent analytical techniques.

19. The method of claim 18 further comprising determining whether the fuel is adulterated based on a comparison of the amount of the fluorescent marking compound in the fuel to a reference standard having a known amount of the marking compound.

20. The method of claim 16 , wherein the agreement between the amount of the fluorescent marking compound determined by the first of the at least two differing and independent analytical techniques and the amount of the fluorescent marking compound determined by the second of the at least two differing and independent analytical techniques is increased by at least about 5%, relative to a same method absent the matrix.