[0001] Method for refining hydrocarbons used as fuels.
Technical Field
[0002] Heterogeneous catalysis of hydrocarbons, refinement.
Background Art
[0003] Liquid hydrocarbons used as fuel, such as gasoline, gas oil or disel, the jet fuel,
or the kerosene, are toxic and of high flammability. Vapors produced by their evaporation
and substances created when burnt, such as carbon monoxide, nitrous oxides, non-burnt
hidrocarbons, etc., contribute to air pollution. Also, burning these fuels additionally
produce carbon dioxide, a greenhouse gas directly related to global climate change.
[0004] Concerned for environment pollution, Governments have passed legislation aimed to
reduce pollutants from hydrocarbons used as fuels. At present time there is a need
for more efficient refining methods. Prior art teaches well known desulfuration methods
for hydrocarbon fractions with organic sulfur compounds impurities.
[0005] Prior art shows a number of alternative gasoline and diese' refining proceses, such
as direct absorption methods (
US4830733A, NAGT et al., 1989), bio-processing methods (
US5910440A, GROSSMAN et al., 1999), selective oxidation methods (
US3341448A, FORD et al., 1967), and zeolites catalysing methods (
MAXWELL, I. E.; STORK, W. H. J. Hydrocarbon processing with zeolites. Studies in Surface
Science and Catalysis, 2001, vol. 137, p. 747-819).
[0006] However, all prior art methods have inconveniences. For example, many of such methods
only can desulfurize hydrocarbons, but fail at reducing bencenes and harmful aromatic
compounds. Additionally, in practice they also entail high costs that hinder their
continuous use.
[0007] Even if prior art refining do remove some polluting components, fuel loses effectiveness
as such compounds help in its combustion.
[0008] Therefore, a refining and catalysing method that removes polluting agents and provides
benefits at low costs is required.
Summary of the invention
[0009] This invention claims a refining and catalysing method for liquid hydrocarbons used
as fuel that eliminates sulfur, aromatic compounds, bencenes, xylenes, toluenes, and
others, and oxidising available octanes to act as comburent during hydrocarbon combustion
processes, producing better burning and more energy availability for industrial fuel
uses.
[0010] The disclosed method is applicable to mixed fuels in the final hydrocarbon refining
step, i.e., fuels that in current state of the art would be used as final products
available in commerce to consumer public.
[0011] The disclosed method comprises mixing small solid ferrous oxide particles mixed with
water vapor until a heterogeneous mixture is achieved. Said heterogeneous mixture
is then poured into a container with substituted hydrocarbons used as fuel, and are
combined and mixed constantly for a few minutes.
[0012] The result is fuel with a lower hydrocarbon count. In gasoline, cyclic hydrocarbons
count is lower, and in diese' and jet fuel lineal hydrocarbon count is reduced.
[0014] Hence, an emulsion is produced which hydrocarbon refining properties are in-disputable,
as may be appreciated in experimental evidence filed as Drawings in this technical
document.
Technical Problem
[0015] Hydrocarbons used in commerce as fuel carry high concentrations of sulfur, aromatic
compounds, bencenes, xylenes, toluenes, and others. Burning these fuels in internal
combustion engines is not efficient enough to burn them all, and are therefore released
in the atmosphere.
Solution to Problem
[0016] A treatment method for reducing polluting agents in liquid substituted hydrocarbons
used as fuel, comprising blending a heterogeneous mixture of ferrous oxide in water
with said fuel, mixing or combining constantly the solution, allow the mixture to
settle, and removing the aqueous solution of ferrous oxide and water by decantation.
Advantageous Effects of Invention
[0017] The fuel obtained as a result of applying the disclosed method contains a lower count
of polluting compounds with sulfur, aromatic compounds, bencenes, xylenes, toluenes,
and others. Additionally, it increases fuel burning efficiency, since during the chemical
reaction hydrocarbons gain additional oxygen atoms that help as comburent.
Brief Description of Drawings
[0018] Disclosed embodiments and their advantages may be better understood making joint
reference to the following description and attached figures. These figures do not
limit in any way the disclosed compound's advantageous effects of its physicochemical
interactions as catalyzer and refiner that a person having ordinary skill in the art
may find, without departing from the disclosed embodiments' spirit and scope. All
figures are graphics resulting from the analysis of the aforementioned hydrocarbon,
performed by gas chromatography with a flame ionization detector (GC-FID) with MS
Perkin Eimer Clarus 580 MS Clarus SQ 85, column Perkin Eimer Elite 5 MS 30 m x0.32
mm DI 0.25µm, and dicloromethane HPLC grade as control solvent, with an inyector temperature
of 250°C, column temperature 50°C / 12 min, of 6°C / 1 min, and 120°C / 10 min, with
an injection volume of 41, and a mobile Helium phase of 0-8 ml/min. These MS conditions
were performed with ionization energy of 70 eV, a transfer temperature of 180°C, and
an ionization source temperature of 200°C.
Fig.1 is the graphic result of the GC-FID analysis of a commercially available diese' sample,
in which the X axis show minutes lapsed, and Y axis shows voltage in mV.
Fig.2 is the graphic result of the GC-FID analysis of a commercially available diese' sample,
treated with the claimed compound and method, in which the X axis show minutes lapsed,
and Y axis shows voltage in mV, and the hydrocarbon reduction is acknowledged.
Fig.3 is the graphic result of the GC-FID analysis of a commercially available gasoline
sample, in which the X axis show minutes lapsed, and Y axis shows voltage in V.
Fig.4 is the graphic result of the GC-FID analysis of a commercially available gasoline
sample, treated with the claimed compound and method, in which the X axis show minutes
lapsed, and Y axis shows voltage in mV, and the hydrocarbon reduction is acknowledged.
Fig.5 is the graphic result of the GC-FID analysis of a commercially available jet fuel
sample, in which the X axis show minutes lapsed, and Y axis shows voltage in mV.
Fig.6 is the graphic result of the GC-FID analysis of a commercially available jet fuel
sample, treated with the claimed compound and method, in which the X axis show minutes
lapsed, and Y axis shows voltage in mV, and the hydrocarbon reduction is acknowledged.
Description of Embodiments
[0019] There is a positive need for a method that reduces polutant agents in liquid substituted
hydrocarbonmixtures used as fuels. Prior art teaches a number of refining steps to
convert oil into usable fuels in the industry. However, these fuels still have sulfur
compounds, aromatic compounds, bencenes, xylenes, bencenes, toluenes, and others that
do not burn adequately when used, and it is therefore necessary a better refining
method to reduce fuels' polluting effects.
[0021] The ferrous oxide supersaturated solution is mixed with the fuel. It is well known
that the ferrous oxide supersaturated solution may be used in a proportion of up to
70% of said solution against 30% fuel. However, in the preferred embodiment, the mixture
is done with 10% solution to 90% fuel, that is, 100 liters of ferrous oxide super-saturated
solution for each 1,000 liters of fuel one wishes to refine.
[0022] The supersaturated solution must be mixed by constant fluid blending, either by agitation,
fluid recirculation, or barometric variations. In the preferred embodiment, 1 liter
of this mixture must be mixed for at least one minute.
[0023] The result of said mixing is a hydrocarbon reduction in the final fuel. In [Fig.1]
it is shown a graphic result of gas chromatography of a commercially available diese'
sample. The first spike belongs to the dichloromethane used as control solvent. In
[Fig.2] it is shown a graphic result of gas chromatography of a commercially available
diese' after treatment with the claimed method. As one can appreciate according to
the retention period shown in [Fig.2], the amount of lineal hydrocarbons has been
reduced, which show the refining capabilities of this method.
[0024] In [Fig.3] it is shown the graphic result of gas chromatography of a commercially
available gasoline sample. The firs spike belongs to the dichloromethane used as control
solvent. In [Fig.4] it is shown the graphic result of gas chromatography of a sample
of the same commercially available gasoline after being treated with the claimed method.
As one can appreciate, the quantity of cyclic hydrocarbons has also decreased.
[0025] [Fig.5] belongs to the analysis to commercially available jet fuel, and [Fig.6] to
the analysis of the same jet fuel after being treated with the claimed method. The
results are similar to those of diese' and gasoline.
Industrial Applicability
[0026] This method is applicable to any industry in which fuel is used and there is a desire
to reduce polluting combustion byproducts, and improve fuel efficiency.
Patent references
References other than patents
[0028]
NPL 1: MAXWELL, I. E.; STORK, W. H. J. Hydrocarbon processing with zeolites. Studies in Surface
Science and Catalysis, 2001, vol. 137, p. 747-819
NPL 2: HAMADA, Hideaki, et al. Role of supported metals in the selective reduction of nitrogen
monoxide with hydrocarbons over metal/alumina catalysts. Catalysis today, 1996, vol.
29, no 1, p. 53-57
NPL 3: MARTIN, Scot T. Precipitation and dissolution of iron and manganese oxides. Environmental
Catalysis, 2005, p. 61-81.