Patent Application
20170130137
The present invention relates to a production method and a production apparatus for producing a hydrocarbon oil.
Recently, the problem of global warming due to the carbon dioxide emission has become serious. In the industrial world, efforts for low emission and the development of alternative energy have been made and certain effects have been achieved. Meanwhile, the nuclear power generation affected by the Great East Japan Earthquake is practically ceased at present, accordingly fossil fuel has to be used more than ever, and thus the emission of carbon dioxide is accelerated.
Today, meanwhile, there is a problem of environmental destruction caused by energy. It is known that fossil fuel contains a sulfur component, a nitrogen component and a phenol component which generate hazardous gas leading to environmental destruction. It is also an urgent task to take a measure against global warming caused by the generation of CO2. In order to prevent or suppress the environmental destruction, it is effective to reduce the generation of hazardous gas which is generated by use of fossil fuel and to improve the fuel efficiency.
As an invention for improving the fuel efficiency of fuel hydrocarbon from such a viewpoint, there is an invention described in Patent Literature 1 performed by the present inventor. The invention disclosed in Patent Literature 1 is an invention in which an active water prepared by mixing a natural plant composite enzyme in water is allowed to react with an oil, and the reacted water also functions as a fuel due to the hydrolysis reaction of the material oil by an enzyme; thus the invention can improve the fuel efficiency, easily suppresses the generation of hazardous substances, provides a production method and a production apparatus for producing a stable fuel oil, and can contribute to the prevention of the environmental destruction.
Patent Document 1: Japanese Patent Laid-Open No. 2012-72199
However, recently, there have been demanded techniques capable of drastically solving the problem of global warming due to the carbon dioxide emission and the problem of alternative energy due to the depletion of fossil fuel. It has already been clarified that fuel hydrocarbons such as gasoline fraction can be produced from the reaction between hydrogen and carbon dioxide; however, reactions under conditions of high temperature and high pressure are required. For a method for synthesizing a hydrocarbon by using carbon dioxide as a material, without using hydrogen as a material, various attempts as implementation of artificial photosynthesis have been performed. However, fuel hydrocarbons have not yet been efficiently produced.
The present invention, made in light of the above-described problems, has an object of providing a method and an apparatus in which methanol is produced by using a carbon dioxide-containing gas or liquid as a material, without needing the conditions of high temperature and high pressure and without addition of hydrogen, and further fuel hydrocarbons such as light oil and heavy oil are produced in good yields.
The present inventor made a diligent study in order to solve the above-described problem, and consequently succeeded in the production of a hydrocarbon oil increased in the amount than the hydrocarbon oil used as a material by mixing a methanol-containing water, a hydrocarbon oil (fuel hydrocarbon), and a carbon dioxide-containing gas or aqueous solution, at normal temperature without being pressurized.
Specifically, the present invention is as follows.
The method for increasing the amount of a hydrocarbon oil according to the present invention is a method in which water bubbled with air in the presence of a catalyst and methanol are mixed, the obtained liquid mixture and a material hydrocarbon oil are mixed to prepare an emulsion, and the emulsion and a carbon dioxide-containing gas or aqueous solution are brought into contact with each other.
The production method for producing a hydrocarbon oil according to the present invention is a production method in which water bubbled with air in the presence of a catalyst and methanol are mixed, the obtained liquid mixture and a material hydrocarbon oil are mixed to prepare an emulsion, the emulsion and a carbon dioxide-containing gas or aqueous solution are subjected to a contact treatment, and a hydrocarbon oil is collected from the resulting treated product.
In the above-described method for increasing the amount of a hydrocarbon oil or the above-described production method for producing a hydrocarbon oil, the hydrocarbon oil is produced on the basis of the following formulas (1) and (2):
CO2+H2O+CnH2n+2=Cn+1+H2n+4+3/2O2 (1)
CH3OH+CnH2n+2=Cn+1H2n+4+H2O (2)
Here, in the above-described method for increasing the amount of a hydrocarbon oil and the above-described production method for producing a hydrocarbon oil, the catalyst is preferably an enzyme and/or a zeolite or a zeolite-like substance (the catalyst may be a substance supported on a zeolite or a zeolite-like substance), water preferably contains an active species, and the hydrocarbon oil is preferably any one of light oil, heavy oil, heating oil, kerosene, and gasoline.
Moreover, the production apparatus for producing a hydrocarbon oil according to the present invention is an apparatus including: a mixing tank for mixing water bubbled with air in the presence of a catalyst and methanol; an emulsion preparation tank for preparing an emulsion by mixing the liquid mixture contained in the mixing tank and a hydrocarbon oil; and a contact tank for bringing the prepared emulsion and carbon dioxide into contact with each other.
Here, the contact tank is preferably a tank in which the emulsion is exposed to carbon dioxide in the atmosphere, or carbon dioxide recovered from any one of the tanks or a carbon dioxide recovery apparatus or the like, or a carbon dioxide-containing gas or aqueous solution is introduced into the emulsion preparation tank.
According to the present invention, the amount of a fuel hydrocarbon can be increased by at least 10% by mixing methanol-containing water, the fuel hydrocarbon, and carbon dioxide. Accordingly, the present invention can produce a fuel hydrocarbon to be an energy source by using carbon dioxide regarded as a cause for global warming as a material, thus can achieve a similar effect as the use of the carbon in the atmosphere as energy by plants through fixing the carbon in the atmosphere by photosynthesis, and can solve both of the energy problem and the environmental problem regarded as the problems of the whole of the earth by the mankind.
The present invention is directed to the increase of a fuel hydrocarbon as follows: methanol-containing water and a fuel hydrocarbon are mixed into an emulsified state, the methanol/water/fuel hydrocarbon mixed solution in an emulsified state and a carbon dioxide-containing gas or aqueous solution are brought into contact with each other, and thus the amount of the fuel hydrocarbon is increased. The fuel hydrocarbon obtained by the method of the present invention is increased in the amount thereof, as compared with the material fuel hydrocarbon, at least by 10%, preferably by 20%, more preferably by 30%, and furthermore preferably by as large as 40%. For example, the proportion of the increased amount of the produced fuel hydrocarbon is 10% to 100%, preferably 10% to 50% and more preferably 30% to 50% of the amount of the material fuel hydrocarbon.
Accordingly, the present invention allows a fuel hydrocarbon to be produced extremely efficiently.
The present invention includes the following steps (i) to (iii).
(i) A water treatment step of activating water by bubbling water with air in the presence of a catalyst.
(ii) A step of preparing an emulsion by mixing the activated water, a hydrocarbon oil, and methanol.
(iii) A step of bringing the emulsion and carbon dioxide into contact with each other.
Here, instead of performing the mixing step after the water treatment step, and further subsequently performing the reaction step, the water treatment step and the mixing step can also be performed simultaneously, the mixing step and the reaction step can be performed simultaneously, and moreover, the water treatment step, the mixing step, and the reaction step can all also be performed simultaneously.
In the present invention, the reactions in the above-described steps (i) to (iii) are represented by the following formulas (1) and (2).
CO2+H2O+CnH2n+2=Cn+1H2n+4+3/2O2 (1)
CH3OH+CnH2n+2=Cn+1H2n+4+H2O (2)
The above-described formula (1) involving carbon dioxide can be represented by the following chain reactions.
CO2+2H2O→CH3OH+3/2O2 (3)
CH3OH+CnH2n+2→Cn+1H2n+4+H2O (4)
The water used is preferably allowed to be in a state of including active species (such as active oxygen and a hydroxyl radical). In order to allow water to include active species, hydroxyl radical is generated in water, or alternatively in the water treatment step, an enzyme such as lipase is mixed in water, or a zeolite or a zeolite-like substance is included in the reaction system. In addition, water is preferably bubbled with air for a predetermined time of period. For example, in order to activate water so as for the reactions represented by the above-described formulas (1) and (2) to be performed at normal temperature, the bubbling is preferably performed at normal temperature for 72 hours; however, depending on the state of the water as a material, the bubbling time may be appropriately altered. The mixing step is preferably performed so as for the reaction mixture to be uniform.
In the present invention, a hydrocarbon oil means a substance mainly composed of a hydrocarbon and exhibiting a liquid state under at normal temperature and normal pressure (for example, a temperature of 15° C. and a pressure of 1 atm), and represented by CnH2n+2 or Cn+1H2n+4 (chain saturated hydrocarbon). Here, n is, for example, 1 to 40, and preferably 1 to 20. Examples of such a hydrocarbon oil include, without being limited to: heavy oil, light oil (for example, n=10 to 20), gasoline (for example, n=4 to 10), naphtha, kerosene (for example, n=10 to 15), heating oil (for example, n=9 to 15), and the like.
In the present description, a hydrocarbon oil is also referred to as a “fuel hydrocarbon” or a “fuel oil.” Similarly, the water bubbled with air in the presence of a catalyst may be also referred to as an “enzyme water” or “water.”
The production method for producing a fuel hydrocarbon according to the present invention can be implemented by utilizing, as the production apparatus thereof, the fuel production apparatus disclosed in Japanese Patent Laid-Open No. 2012-72199. In other words,
To a mixing tank 11a, for example, soft water and a zeolite or a zeolite-like substance containing an enzyme powder (for example, EP-10) are fed in a proportion of 1000 liters and 500 g; the soft water, the enzyme powder and zeolite are stirred and mixed for, for example, 72 hours by the air supplied from a blower pump 15. The ratio of the water and the zeolite or zeolite-like substance containing an enzyme powder is preferably, for example, approximately 0.05% (weight ratio) of an enzyme powder with respect to 99.95% (weight ratio) of the soft water. The origin of the enzyme constituting the enzyme powder is not particularly limited; the enzyme may be derived from animal, plant, or microorganism. Preferably, the enzyme contains lipase as a main component, and more preferably is formed of lipase and cellulase. It is more preferable that the enzyme contains 98% (weight ratio) of lipase and 2% (weight ratio) of cellulase. Such an enzyme can be extracted from fruits such as mango, avocado, pineapple, noni, sea buckthorn, and the like. Commercially available enzymes are also be utilized. Preferably, the enzyme powder is obtained by thermally drying such an enzyme and used with improved preservability.
The resultant water mixture is transferred to the next mixing tank 11b by the pump P after a certain time period. During the transfer, impurities are removed by the filter F. In the mixing tank 11b, the water mixture are again stirred and mixed by air supplied from the blower pump 15. This cycle is repeated until being finished in the mixing tank 11d, the water mixture is transferred from the mixing tank 11d to the stabilizing tank 14, and then alcohol is added to the water mixture in the stabilizing tank 14. This alcohol may be, for example, methanol or ethanol, and methanol is preferable. A preferable ratio of the alcohol is, for example, about 5% to 20% (weight ratio) of methanol with respect to the water mixture.
The active water refined with alcohol is taken out from the stabilizing tank 14 by the pump P. During this process, impurities are removed by three filters F. The refined active water which is taken out is transferred to a different appropriate container or stored in an active water tank 22 of a uniformly mixing apparatus 2 shown in
In the present embodiment, the water activated by the water treatment apparatus 1 is activated so as to perform the reactions of the reaction formulas (1) and (2) even at normal temperature when a material oil is added in the reaction step.
The material oil tank 21 is a tank for storing oil used as a material, and feeds the material oil stored therein by a unit of necessary amount into the stirring tanks 23 through a pipe R. The material oil may be, for example, A—heavy oil, B—heavy oil, C—heavy oil, light oil, kerosene or the like. In the present embodiment, A-heavy oil is used.
The active water tank 22 is a tank for storing active water refined by the water treatment apparatus 1, and feeds the active water stored therein by a unit of necessary amount into the stirring tanks 23 through the pipe R.
The stirring tanks 23 are each a tank for producing fuel oil by stirring and thus reacting the fed material oil (for example, A-heavy oil) with the active water. The reaction here is a hydrolysis reaction of the material oil by the enzyme. The ratio of the material oil and the active water to be fed into the stirring tanks 23 may be appropriately adjusted in accordance with the type of the material oil. For example, a preferable ratio is 60% of A-heavy oil and 40% of the active water, 70% of light oil and 30% of the active water, or 70% of kerosene and 30% of the active water.
The control board 24 is a control section for controlling the elements of the apparatus, and executes various types of controls, for example, turns power supply on or off. The pulse adding section 25 vibrates the fuel oil produced in the stirring tanks 23 so that residue is easily removed. The residue is, for example, water which was left unreacted, impurities in the heavy oil, or the like.
The Newton's separation tank 26 stores the fuel oil and drops the residue downward by the force of gravity, and thus extracts the fuel oil remaining in an upper part thereof.
The separation tank 27 further separates the residue from the fuel oil. The precision filter 28 removes the residue from the fuel oil by a filter. The finishing tank 29 stores the produced refined fuel oil. The waste liquid tank 30 stores a waste liquid generated in the pulse adding section 25 and the Newton's separation tank 26.
The pump 44L is connected to a pipe having a suction opening 41L in an upper part thereof. The pump 44L feeds the fuel oil, active water, or active water-oil mixture to the stirrer 43L, and thus generally uniformly circulates the fuel oil, active water, or active water-oil mixture in the stirring space 40.
The pump 44R is connected to a pipe having a suction opening 41R in a lower part thereof. The pump 44R feeds the fuel oil, active water, or active water-oil mixture to the stirrer 43R, and thus generally uniformly circulates the fuel oil, active water, or active water-oil mixture in the stirring space 40. As each of the pumps 44L and 44R, it is preferable to use a 30 to 40 atmospheric pressure pump.
The head 51 has an inflow opening 57 in a part of a side surface thereof, through which the fuel oil, active water, or active water-oil mixture flows to the inside. The inflow opening 57 is a hole running from the outside to the inside of the head 51, and is surrounded by a cylindrical connection cover 55. The connection cover 55 has a thread groove 56 in an inner surface thereof, such that the pipe connected to the pump 44 is attachable thereto.
As shown in
As shown in
In the trailing end section 60 of the stirrer 43, a discharge hole 61 is provided. The stirrer 43 thus structured can stir oil and active water efficiently to cause a decomposing reaction. In more detail, the fuel oil, active water, or active water-oil mixture flowing to the inside through the inflow opening 57 rotates around the central shaft 53 while moving toward the discharge hole 61 with the rotation radius thereof being gradually decreased in a whirlwind manner. During this process, the fuel oil, active water, or active water-oil mixture is stirred by the plurality of pins 63 provided in the stirrer 43. By the rotation in a whirlwind manner, a negative pressure is generated in a lower part of the central axis 53, which allows the fuel oil, active water, or active water-oil mixture to flow to the inside through the inflow opening 53a. Namely, the stirrer 43L shown in
While being stirred in the stirring tank 23 having the stirrer 43 for a predetermined time period (for example, about 15 to 20 minutes), the oil and the active water stirred while moving in a whirlwind manner in the stirrer 43 contact each other 300 to 500 times. Thus, the hydrolysis reaction is promoted, and the molecules become smaller and the specific gravity is decreased.
The partitions 71 are slowly twisted inside like a screw, and vibrates the fuel oil flowing to the inside to promote the reaction. Owing to this, the fuel oil is put into a state where impurities are easily removed.
The filter 81 is provided radially. As shown in
Owing to this structure, the fuel oil flows to the inside through the liquid inflow opening 91 into a first storage section 90a. Impurities thereof are accumulated in a lower part thereof, and the refined fuel oil is stored in an upper part thereof and overflows into a second storage section 90b next to the first storage section 90a. This process is repeated from the first storage section 90a to a fourth storage section 90d, and the resultant clean fuel oil is discharged from the liquid discharge opening 95.
The impurities precipitated in the storage sections 90a to 90d move downward along the inclining plate 96. For this process, the movable plates 94 are opened to allow the impurities to move downward. The movable plates 94 are not opened in the opposite direction and so the impurities do not flow in the opposite direction.
The impurities moved downward along the inclining plate 96 are transferred from a recovery opening 97 to a recovery section 98 via a valve 99a and are recovered in the recovery section 98. The valve 99a is opened and closed intermittently. When the residue is stored in a certain amount, the valve 99a is opened to allow the residue to be recovered in the recovery section 98 and then is closed. Then, air is discharged via an air discharge valve 99c provided in an upper part of the recovery section 98. The impurities recovered in the recovery section 98 may be taken out via a recovery valve 99b and discarded.
As the stirrer 43, a different type of stirrer 43A as shown in
A fuel oil can be produced by performing the reactions represented by the reaction formulas (1) and (2), by using the above-described water treatment apparatus 1, uniformly mixing apparatus 2 and Newton's separation tank 26.
Hereinafter, the present invention is described more specifically by way of Examples. However, the present invention is not limited to these Examples.
Production Test of Fuel Oil
The present inventor performed a production test of a fuel hydrocarbon by using the above-described apparatuses. The test used the apparatuses described in the above-described embodiment for carrying out the invention, and adopted the methods described in the same embodiment.
<Test Results>
In the present test, light oil was used as a material oil, and as a new oil, a fuel prepared by mixing the material oil and methanol/active water (mixing volume ratio was 370:150) was able to be obtained.
In the present test, the fed substances are as follows.
Compared with this, the total of the overflowed new fuel and the residual amounts in the respective tanks is as follows.
Consequently, the balance of the light oil was +1317.88 kg, the methanol enzyme water balance was −1934.80 kg, the total balance was −616.92 kg, and the increment rate of light oil reached as large as 46.36%.
Additional Test
A similar additional test performed after Example 1 also yielded the following data.
Total substance balance −16.0 kg
Light oil 126.5 kg
Water −117.1 kg
Methanol −25.3 kg
Increment rate of light oil 40.2%
A continuous 9-batch (370 liters of light oil in a batch) production test was performed.
Fed light oil: 2813.85 kg
Produced light oil: 3826.88 kg
Increment rate of light oil: 36%
Fed amount (total: 9768.1 kg)
Preparation of Newton's Tank
Methanol enzyme water (load cell measured value: 7036.0 kg, methanol concentration: 0.786%)
(Items: enzyme water (6980.7 kg), methanol (55.3 kg), light oil (none))
Total amount fed in 1 course (6 batches)
Methanol enzyme water: 868.6 kg ((i) 145.3, (ii) 144.0, (iii) 145.6, (iv) 143.6, (v) 145.2, (vi) 144.9) kg
Light oil: 1863.5 kg (2218.45 l, specific gravity: 0.840) ((i) 310.3, (ii) 310.3, (iii) 311.1, (iv) 310.3, (v) 311.3, (vi) 310.2) kg
(Fundamental preparation: enzyme water 130 kg/130 l, methanol 25.7 kg/32.5 l, light oil 319.2 kg/380 l)
Recovered amount (total: 9608.6 kg)
After completion of the total course of 1 course (6 batches), the masses were measured by manual operations.
Methanol enzyme water: 7092.7 kg
Light oil: 2515.9 kg (2995.12 liters, specific gravity: 0.84)
Mass balance (−159.5 kg)
Fed amount−recovered amount=9768.1 kg−9608.6 kg=−159.5 kg
According to the measurement value of the load cell, the total weight was found to be −140 kg, and hence the substantial mass increase or decrease was approximately 19.5 kg.
Increase or decrease of methanol enzyme water: −811.9 kg (fed amount 7904.6 kg−recovered amount 7092.7 kg)
Increase or decrease of light oil: +652.4 kg (fed amount 1863.5 kg−recovered amount 2515.9 kg, 776.6 liters}
Light oil increment rate: 35.0%
Verification of Test Results
On the basis of the substance balance data of the above-described test results, the carbon source of the light oil increased in amount was verified.
First, by verifying the carbon source of the amount increase of the light oil based on the substance balance data, the following points were clarified from the substance balance data obtained by the production of the new fuel.
1) The decreased amount of methanol alone was not able to elucidate the increased amount of light oil, and thus it was clarified that another carbon source was involved.
2) The decrease of the amount of water was clearly observed, and hence a carbon source other than methanol is required; accordingly, it is necessary to consider that a chemical reaction formula (1) (the involvement of carbon dioxide in the reaction consumes water) holds; thus, the carbon dioxide in the air may be safely considered to be a carbon source for the amount increase of light oil.
From the foregoing discussion, a carbon source other than methanol is required, and the involvement of carbon dioxide in the reaction consumes water, and hence it has been shown that the carbon dioxide in the air can be a carbon source for the amount increase of light oil. The result that the production rates of light oil in Examples 1 and 2 are different from each other may be ascribable to the conditions that as can be seen from the formulas (1) to (4), water is a material for the amount increase of light oil, and the production rate is varied, for example, depending on the nature (pH, hardness, turbidity and others) of the water; however, foregoing Examples have verified that approximately 30% or more of the amount increase is possible.
Verification of Carbon Source
In order to investigate whether or not carbon dioxide was a carbon source for the amount increase of light oil, a verification of the introduction of a stable carbon isotope 13C into the hydrocarbon in the light oil was performed according to the following procedures.
1) A PET bottle (vessel 1) having an internal volume of 500 ml was filled with CO2 labeled with 13C and sealed tightly.
2) In the vessel 1, 100 g of a liquid mixture (liquid temperature: 30.5° C.) flowing out from a pulse tank was placed and the vessel was sealed tightly.
3) The vessel was shaken for approximately 5 seconds and then allowed to stand still. During the shaking, it was verified that the vessel 1 was crushed.
4) After 6 days from the completion of the above-described operations, the stable carbon isotope ratio δ13C was measured by using the DELTA V ADVANTAGE of Thermo Fischer Scientific K.K.
This measurement was performed at Isotope Research Institute, Inc. (in Yokohama City Industry-Academia Colloborative Research Center, 1-1-40 Suehiro-cho, Tsurumi-ku, Yokomama, CEO: Akira Hanawa).
According to the results of two runs of analysis (analysis 1 and analysis 2), the stable carbon isotope ratio (δ13C vs PDB) was −26.4(%) in the analysis 1 and −27.8(%) in the analysis 2.
In other words, the result shows that the δ13C of the light oil brought into contact with 13C was higher by 1.4% than the δ13C of the original light oil. This shows that the content of 13C was higher as compared with the original light oil. Consequently, carbon dioxide was demonstrated to be a carbon source for the amount increase of light oil.
As described above, the substance balance in the production of the new fuel and the reaction test using the stable carbon isotope 13C demonstrated that as the carbon source for the amount increase of light oil, not only methanol but also carbon dioxide is involved.
In other words, when the carbon of the carbon dioxide in the atmosphere was used as the carbon source, the carbon was able to be artificially fixed, and it was secondarily shown that a fuel (light oil in the above-described examples) is synthesized (increased in amount) by using such carbon. According to the chemical reaction formulas implemented by the present invention, carbon dioxide was taken and oxygen was released, and thus carbon is converted into an energy source in a form of a fuel; accordingly, it is obvious that there occurs a reaction capable of being safely referred to as an artificial photosynthesis. Surprisingly, the reactions based on the above-described reaction formulas (1) and (2) were implemented, in Examples of the present invention, at normal temperature, without applying a high temperature and a high pressure. Of course, the present invention is not limited only to the case where the reactions based on the reaction formulas (1) and (2) are all performed at normal temperature. For example, by performing some steps under warming or under pressure, in a further shorter time, a high performance methanol or a fuel hydrocarbon can also be produced.
In above-described Examples, carbon dioxide was allowed to react with a fuel (light oil); however, the carbon taken in according to the reaction formula (1) can be utilized as methanol, accordingly, the methanol can be processed into materials of various chemical products or into a fuel itself, and thus the application range of such carbon is wide.
Moreover, recently, a large number of apparatuses for recovering carbon dioxide from burnt gas have been disclosed. At present, the carbon dioxide recovered from such an apparatus is discarded in the earth crust in the deep underground; however, the recovered carbon dioxide can be incorporated into the reaction system of the present invention, thus the effect of carbon circulation is created, combustion is made possible without increasing the amount of carbon dioxide in the atmosphere; in this case, high-concentration carbon dioxide can be allowed to react, and more efficient production of methanol or a fuel can be performed.
From the above-described description, the present invention can be said to be an epoch-making technique also from the viewpoint of the global environment.
Herein, for the stable carbon isotope ratio (δ13C: delta 13C), some additional remarks are presented. In other words, a direct measurement of the absolute concentration an element or an isotope is extremely difficult, and accordingly, a method for measuring the relative abundance ratios of isotopes is generally adopted. The stable isotope ratio δ is represented in terms of permillage ( 1/1000: permil) by how the stable isotope abundance ratio of a standard substance and the stable isotope abundance ratio of an analysis sample are separated (deviated) from each other. The standard substance of carbon (C) is the belemnite (PDB: Pee Dee Belemnite, the calcium carbonate of the belemnite (a fossil of a squid) produced in the Pee Dee stratum in the North Carolina State, United States of America), the content of 12C being 98.894% and the content of 13C being 1.106%.
Verification of Example 4
In the description until Example 4, it has been theoretically verified that carbon dioxide is the carbon source for the amount increase of the hydrocarbon oil; however, herein, a test was actually performed on the amount increase due to the presence of carbon dioxide. Because of the structure of the apparatus, the structure cannot perfectly shield the carbon dioxide (for example, in the atmosphere), and hence a test was performed on the behavior in the case where carbon dioxide was compulsorily exposed.
<Test Procedure 1>
The liquid mixture flowing out from the pulse tank was sampled in an amount of 50 g, and placed in a 500-ml sealed vessel; and the degree of the amount increase was measured under the following conditions. The measurement was performed after 1 hour from the above-described sampling.
(i) The case where the space in the vessel was filled with air (in the usual case, the concentration of carbon dioxide was approximately 300 ppm)
Amount increase: Approximately 15%
(ii) The case where the space in the vessel was completely filled with carbon dioxide
Amount increase: Approximately 26%
The amount increase found even in (i) is ascribable to the open structure of the interior of the stirring tank/the pulse tank and the reaction mixture is exposed to the atmosphere, and the reaction of the fed methanol. The difference between (i) and (ii) is the concentration of the exposed carbon dioxide; the large amount increase found in (ii) can be ascribable to the high concentration of the carbon dioxide exposed to the liquid mixture and the thereby accelerated reaction.
From the above-described test, after 1 hour, the difference between the amount increases was able to be verified so as to suggest the shortening of the reaction time by the presence of carbon dioxide, and accordingly, a test was performed on the reaction time difference due to the difference in the concentration of carbon dioxide.
<Test Procedure 2>
The liquid mixture flowing out from the pulse tank was sampled in an amount of 50 g, and placed in a 500-ml sealed transparent vessel; and the time course of the amount increase was measured under the following conditions.
The time for approximately 30% of the amount increase: approximately 22 hours
The time for approximately 30% of the amount increase: approximately 90 minutes
From the above-described test results, the possibility of the shortening of the reaction time by positively exposing carbon dioxide was able to be verified.
By using an oxygen detecting tube, it was qualitatively verified whether or not oxygen was actually generated during the reaction as in the chemical reaction formula (1) CO2+H2O+CnH2n+2=Cn+1H2n+4+3/2O2 showing the generation of oxygen.
<Test Procedure>
During the operation of the stirring tank, the gas in the upper portion of the tank was sampled, and the oxygen concentration was measured with an oxygen detecting tube. The same measurement was also performed for the atmosphere (background) in the vicinity of the tank.
Oxygen concentration: Approximately 21%
Oxygen concentration: Approximately 22.5% to 23%
From the results of the test, the generation of oxygen in the above-described chemical reaction formula (1) was able to be verified.
The present invention can be utilized for increasing the amounts of various oils such as A—heavy oil, B—heavy oil, C—heavy oil, light oil, kerosene and the like.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2014-069467 | Mar 2014 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2015/059966 | 3/30/2015 | WO | 00 |
