JP4848614B2 - Hydrogen storage method - Google Patents

Description

  The present invention relates to a hydrogen storage method capable of stably storing hydrogen in a relatively light state and in a state close to room temperature and normal pressure, and easily removing the stored hydrogen.

In recent years, a new clean energy system using hydrogen as an energy medium has been proposed as a measure for dealing with global environmental problems associated with CO ₂ emissions. Fuel cells, in particular, are energy conversion technologies that extract the chemical energy generated when hydrogen combines with oxygen into water, and are used as electric energy. Power sources that replace gasoline engines in automobiles, home on-site power generation, and IT As a DC power supply facility, it is attracting attention as one of the most important technologies of the next generation.

  However, the biggest problem with hydrogen fuel lies in its storage and transportation methods.

  That is, conventionally, various methods for storing hydrogen have been proposed, and one of them is a method for storing hydrogen as a gas in a high-pressure gas cylinder. However, although such high-pressure storage is simple, a thick container is required, and therefore the weight of the container is heavy, and the storage and transport efficiency is low. Application is difficult. On the other hand, when hydrogen is stored as a liquid, the storage / transport efficiency is improved as compared with gaseous hydrogen, but high-purity hydrogen is required for the production of liquid hydrogen, and the liquefaction temperature is −252. There is an economical problem such as a low temperature of 6 ° C. and the need for such a special container for ultra-low temperatures. It has also been proposed to use a hydrogen storage alloy, but the weight of the alloy itself is heavy, and there is a problem that the operating temperature for releasing hydrogen is high at a temperature close to 300 ° C. in a lightweight Mg-based hydrogen storage alloy. . Furthermore, the use of porous carbon materials such as carbon nanotubes has also been proposed, but the hydrogen storage has low reproducibility, storage under high pressure conditions, and the production of carbon nanotubes is not easy. There's a problem.

As a novel hydrogen storage method for hydrogen that solves the above-described conventional problems, the applicant of the present invention is a hydrogen that is relatively light and close to normal temperature and normal pressure by bringing hydrogen gas into contact with an organic compound in a pressurized state. And found that it can be easily stored as a hydrogen molecule compound or the like that can be stably held, and previously filed a patent application (Japanese Patent Application No. 2003-24590).
Japanese Patent Application No. 2003-24590

  The hydrogen storage method of Japanese Patent Application No. 2003-24590 is a hydrogen storage method that can stably store hydrogen in a relatively light state and in a state close to normal temperature and normal pressure, and can easily take out the stored hydrogen. Further improvement of hydrogen storage efficiency is desired.

  Accordingly, an object of the present invention is to provide a method for efficiently storing hydrogen in an organic compound.

The hydrogen storage method according to claim 1 of the present invention is a hydrogen storage method in which hydrogen is taken into a solid substance obtained by cooling after bringing an organic compound in a gaseous state and hydrogen gas into contact with each other, The organic compound is a compound that forms a hydrogen molecule compound upon contact with hydrogen gas, the hydrogen molecule compound is a hydrogen clathrate compound using the organic compound as a host compound, and the organic compound is urea, 1, 1,6,6-tetraphenylhexa-2,4-diyne-1,6-diol, 1,1-bis (2,4-dimethylphenyl) -2-propyn-1-ol, 1,1,4, 4-tetraphenyl-2-butyne-1,4-diol, 1,1,6,6-tetrakis (2,4-dimethylphenyl) -2,4-hexadiyne-1,6-diol, 9,10-diphenyl -9,10-jihi Loanthracene-9,10-diol, 9,10-bis (4-methylphenyl) -9,10-dihydroanthracene-9,10-diol, 1,1,2,2-tetraphenylethane-1,2- Diol, 4-methoxyphenol, 2,4-dihydroxybenzophenone, 4,4′-dihydroxybenzophenone, 2,2′-dihydroxybenzophenone, 2,2 ′, 4,4′-tetrahydroxybenzophenone, 1,1-bis ( 4-hydroxyphenyl) cyclohexane, 4,4′-sulfonylbisphenol, 2,2′-methylenebis (4-methyl-6-tert-butylphenol), 4,4′-ethylidenebisphenol, 4,4′-thiobis (3- Methyl-6-tert-butylphenol), 1,1,3-tris (2-methyl-4-hydroxy-5-t-) Butylphenyl) butane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethylene, 1,1,2,2-tetrakis (3 -Methyl-4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (3-fluoro-4-hydroxyphenyl) ethane, [alpha], [alpha], [alpha] ', [alpha]'-tetrakis (4-hydroxyphenyl) -p Xylene, tetrakis (p-methoxyphenyl) ethylene, 3,6,3 ', 6'-tetramethoxy-9,9'-bi-9H-xanthene, 3,6,3', 6'-tetraacetoxy-9 , 9′-bi-9H-xanthene, 3,6,3 ′, 6′-tetrahydroxy-9,9′-bi-9H-xanthene, gallic acid, methyl gallate, catechin, bis-β-naphthol, α , Α, α ', α'-tetraphenyl-1,1'-biphenyl-2,2'-dimethanol, diphenic acid bisdicyclohexylamide, fumaric acid bisdicyclohexylamide, cholic acid, deoxycholic acid, 1,1,2,2-tetraphenyl Ethane, tetrakis (p-iodophenyl) ethylene, 9,9'-beananthryl, 1,1,2,2-tetrakis (4-carboxyphenyl) ethane, 1,1,2,2-tetrakis (3-carboxyphenyl) Ethane, acetylenedicarboxylic acid, 2,4,5-triphenylimidazole, 1,2,4,5-tetraphenylimidazole, 2-phenylphenanthro [9,10-d] imidazole, 2- (o-cyanophenyl) ) Phenanthro [9,10-d] imidazole, 2- (m-cyanophenyl) phenanthro [9,10- ] Imidazole, 2- (p-cyanophenyl) phenanthro [9,10-d] imidazole, hydroquinone, 2-t-butylhydroquinone, 2,5-di-t-butylhydroquinone, and 2,5-bis (2, It is one or more selected from the group consisting of 4-dimethylphenyl) hydroquinone .

The hydrogen storage method according to claim 2 of the present invention is a hydrogen storage method in which hydrogen is taken into the organic compound by heating the solid organic compound in a hydrogen gas atmosphere and then cooling it. The compound is a compound that forms a hydrogen molecule compound by contact with hydrogen gas, the hydrogen molecule compound is a hydrogen clathrate compound using the organic compound as a host compound, and the organic compound is urea, 1, 1, 6,6-tetraphenylhexa-2,4-diyne-1,6-diol, 1,1-bis (2,4-dimethylphenyl) -2-propyn-1-ol, 1,1,4,4- Tetraphenyl-2-butyne-1,4-diol, 1,1,6,6-tetrakis (2,4-dimethylphenyl) -2,4-hexadiyne-1,6-diol, 9,10-diphenyl-9 , 10-di Droanthracene-9,10-diol, 9,10-bis (4-methylphenyl) -9,10-dihydroanthracene-9,10-diol, 1,1,2,2-tetraphenylethane-1,2- Diol, 4-methoxyphenol, 2,4-dihydroxybenzophenone, 4,4′-dihydroxybenzophenone, 2,2′-dihydroxybenzophenone, 2,2 ′, 4,4′-tetrahydroxybenzophenone, 1,1-bis ( 4-hydroxyphenyl) cyclohexane, 4,4′-sulfonylbisphenol, 2,2′-methylenebis (4-methyl-6-tert-butylphenol), 4,4′-ethylidenebisphenol, 4,4′-thiobis (3- Methyl-6-tert-butylphenol), 1,1,3-tris (2-methyl-4-hydroxy-5-t) -Butylphenyl) butane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethylene, 1,1,2,2-tetrakis ( 3-methyl-4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (3-fluoro-4-hydroxyphenyl) ethane, α, α, α ′, α′-tetrakis (4-hydroxyphenyl)- p-xylene, tetrakis (p-methoxyphenyl) ethylene, 3,6,3 ′, 6′-tetramethoxy-9,9′-bi-9H-xanthene, 3,6,3 ′, 6′-tetraacetoxy- 9,9′-bi-9H-xanthene, 3,6,3 ′, 6′-tetrahydroxy-9,9′-bi-9H-xanthene, gallic acid, methyl gallate, catechin, bis-β-naphthol, α, α, α ' , Α′-tetraphenyl-1,1′-biphenyl-2,2′-dimethanol, diphenic acid bisdicyclohexylamide, fumaric acid bisdicyclohexylamide, cholic acid, deoxycholic acid, 1,1,2,2-tetra Phenylethane, tetrakis (p-iodophenyl) ethylene, 9,9'-bianthryl, 1,1,2,2-tetrakis (4-carboxyphenyl) ethane, 1,1,2,2-tetrakis (3-carboxyphenyl) ) Ethane, acetylenedicarboxylic acid, 2,4,5-triphenylimidazole, 1,2,4,5-tetraphenylimidazole, 2-phenylphenanthro [9,10-d] imidazole, 2- (o-cyano) Phenyl) phenanthro [9,10-d] imidazole, 2- (m-cyanophenyl) phenanthro [9,10 d] imidazole, 2- (p-cyanophenyl) phenanthro [9,10-d] imidazole, hydroquinone, 2-t-butylhydroquinone, 2,5-di-t-butylhydroquinone, and 2,5-bis (2 , 4-Dimethylphenyl) hydroquinone, which is one or more selected from the group consisting of .

  That is, the present inventor has conducted extensive studies on a method for efficiently storing hydrogen in an organic compound, and as a result, the organic compound in a gaseous state is brought into contact with hydrogen gas and then cooled, or a hydrogen gas atmosphere It is easy and efficient as a hydrogen molecule compound that can hold hydrogen in the organic compound relatively lightly and under conditions close to normal temperature and normal pressure by heating a solid organic compound and then cooling it. It was found that it can be incorporated automatically.

  In the present invention, the organic compound does not include those composed only of carbon atoms such as graphite, carbon nanotubes, fullerenes, and includes organometallic compounds including a metal component.

  In addition, the molecular compound referred to in the present invention is a relatively weak interaction other than a covalent bond, in which two or more kinds of compounds that can exist stably alone are represented by hydrogen bonds and van der Waals forces. And includes hydrates, solvates, addition compounds, inclusion compounds, and the like. Such a hydrogen molecule compound can be formed by a catalytic reaction under pressure between an organic compound that forms a hydrogen molecule compound and hydrogen, and can store hydrogen in a relatively lightweight state close to normal temperature and pressure. In addition, hydrogen can be released from the hydrogen molecular compound by simple heating or the like.

Hydrogen molecular compound according to the present invention is a hydrogen clathrate compound clathrate hydrogen molecules by contact reaction between the organic compound and hydrogen molecules.

  According to the hydrogen storage method of the present invention, hydrogen can be stored under normal temperature and normal pressure conditions, so that a pressure vessel, a low temperature vessel, etc. are unnecessary, and hydrogen is stored and transported in a relatively small and light state. In addition, the stored hydrogen can be easily released and used for various purposes.

  Hereinafter, embodiments of the hydrogen storage method of the present invention will be described in detail.

In the present invention, the organic compound used in the storage of hydrogen, an organic compound except those consisting solely of carbon atoms, Ru der it can store hydrogen by contacting with hydrogen gas under pressure.

As the organic compound which forms a hydrogen clathrate compound clathrate of hydrogen molecules, as a multi-molecular host compound, urea, 1,1,6,6-tetraphenyl-hexa-2,4-diyne -1, 6-diol, 1,1-bis (2,4-dimethylphenyl) -2-propyn-1-ol, 1,1,4,4-tetraphenyl-2-butyne-1,4-diol, 1,1 , 6,6-tetrakis (2,4-dimethylphenyl) -2,4-hexadiyne-1,6-diol, 9,10-diphenyl-9,10-dihydroanthracene-9,10-diol, 9,10- Bis (4-methylphenyl) -9,10-dihydroanthracene-9,10-diol, 1,1,2,2-tetraphenylethane-1,2-diol, 4-methoxyphenol, 2,4-dihydroxybenzo F Non, 4,4′-dihydroxybenzophenone, 2,2′-dihydroxybenzophenone, 2,2 ′, 4,4′-tetrahydroxybenzophenone, 1,1-bis (4-hydroxyphenyl) cyclohexane, 4,4′- Sulfonyl bisphenol, 2,2′-methylene bis (4-methyl-6-tert-butylphenol), 4,4′-ethylidene bisphenol, 4,4′-thiobis (3-methyl-6-tert-butylphenol), 1,1 , 3-Tris (2-methyl-4-hydroxy-5-t-butylphenyl) butane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (4 -Hydroxyphenyl) ethylene, 1,1,2,2-tetrakis (3-methyl-4-hydroxyphenyl) ethane, 1,1,2,2-the Trakis (3-fluoro-4-hydroxyphenyl) ethane, α, α, α ′, α′-tetrakis (4-hydroxyphenyl) -p-xylene, tetrakis (p-methoxyphenyl) ethylene, 3,6,3 ′ , 6′-Tetramethoxy-9,9′-bi-9H-xanthene, 3,6,3 ′, 6′-tetraacetoxy-9,9′-bi-9H-xanthene, 3,6,3 ′, 6 '-Tetrahydroxy-9,9'-bi-9H-xanthene, gallic acid, methyl gallate, catechin, bis-β-naphthol, α, α, α', α'-tetraphenyl-1,1'-biphenyl -2,2'-dimethanol, diphenic acid bisdicyclohexylamide, fumaric acid bisdicyclohexylamide, cholic acid, deoxycholic acid, 1,1,2,2-tetraphenylethane, tetrakis (p-iodophenyl) Tylene, 9,9′-bianthryl, 1,1,2,2-tetrakis (4-carboxyphenyl) ethane, 1,1,2,2-tetrakis (3-carboxyphenyl) ethane, acetylenedicarboxylic acid, 2,4 , 5-triphenylimidazole, 1,2,4,5-tetraphenylimidazole, 2-phenylphenanthro [9,10-d] imidazole, 2- (o-cyanophenyl) phenanthro [9,10-d] Imidazole, 2- (m-cyanophenyl) phenanthro [9,10-d] imidazole, 2- (p-cyanophenyl) phenanthro [9,10-d] imidazole, hydroquinone, 2-t-butylhydroquinone, 2,5 - di -t- butyl hydroquinone, and 2,5-bis (2,4-dimethylphenyl) Hidorokino down.

  Among the compounds described above, 1,1-bis (4-hydroxyphenyl) cyclohexane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (4 -Hydroxyphenyl) phenolic host compounds such as ethylene, diphenic acid bis (dicyclohexylamide), amide based host compounds such as fumaric acid bisdicyclohexylamide, 2- (m-cyanophenyl) phenanthro [9,10-d] An imidazole host compound such as imidazole is advantageous in terms of inclusion ability, and in particular, a phenol host compound such as 1,1-bis (4-hydroxyphenyl) cyclohexane is advantageous in terms of easy industrial use. It is.

  These host compounds may be used individually by 1 type, and may use 2 or more types together.

  In the method of claim 1, the form of the organic compound to be used may be any of a solid, a liquid, and a gas under normal temperature and normal pressure, as long as it can be gasified by heating or the like and becomes a solid by cooling. Although there is no limitation, a solid organic compound at normal temperature and pressure is preferable in that it does not require new energy when cooled to a solid state.

  A host compound such as 1,1-bis (4-hydroxyphenyl) cyclohexane described above is known to incorporate various guest molecules to form a crystalline inclusion compound. It is also known that an inclusion compound is formed by direct contact reaction with a guest compound (which may be in a solid, liquid, or gas state). According to the first aspect of the present invention, hydrogen molecules are brought into contact with an organic compound as a host compound in a gaseous state by contacting gas molecules called hydrogen gas in a gaseous state so that the hydrogen molecules can be efficiently incorporated into the clathrate compound to stably store hydrogen. it can.

  As a condition for bringing hydrogen into contact with the organic compound, the condition of the organic compound is not particularly limited as long as it is in a gaseous state. The heating temperature in that case should just be not high temperature which the said organic compound will decompose | disassemble, and there is no restriction | limiting in particular, Generally room temperature-about 300 degreeC are preferable.

  Moreover, as a method of cooling the organic compound gasified by heating etc., the method of naturally cooling at normal temperature may be sufficient, and you may cool rapidly or forcibly using a cooling medium.

On the other hand, the hydrogen condition is not particularly limited as long as hydrogen is in a gaseous state, and may be in a normal temperature, high temperature, or low temperature state. Moreover, there is no restriction | limiting in particular also about the pressure conditions of hydrogen gas, However, It is preferable that it is 1.0 * 10 < ^-10 > -200MPa, Especially 0.1-70MPa.

  Moreover, there is no restriction | limiting in particular about the time which makes the gasified organic compound and hydrogen gas contact, However It is preferable to set it as about 0.01 to 24 hours from surfaces, such as working efficiency.

  In the method of claim 2, a solid organic compound is used.

  The organic compound is preferably a powdered solid from the viewpoint of contact efficiency with hydrogen gas, etc., but is not limited to this, and may be granular or agglomerated, and may be crystalline or amorphous. Any of (amorphous) may be used. When the organic compound is a powdery solid, the particle size is not particularly limited, but in general, it is preferably about 1 mm or less.

  These organic compounds can also be used as an organic compound-containing composite material supported on a porous material. In this case, the porous material supporting the organic compound includes, but is not limited to, intercalation compounds such as clay minerals and montmorillonites in addition to silicas, zeolites and activated carbons. . Such an organic compound-containing composite material is prepared by, for example, dissolving the above-described organic compound in a solvent that can dissolve the organic compound, impregnating the solution in a porous material, drying the solvent, and drying under reduced pressure. Can be manufactured. Although there is no restriction | limiting in particular as the load of the organic compound with respect to a porous material, Usually, it is about 10 to 80 weight% with respect to a porous material.

  In the invention of claim 2, hydrogen molecules are brought into contact with an organic compound as a host compound at a high temperature to cause hydrogen molecules to be efficiently incorporated into the clathrate compound, thereby stably storing hydrogen. it can.

  The heating temperature at the time of bringing hydrogen into contact with the organic compound is not particularly limited as long as the temperature is equal to or lower than the melting point or decomposition temperature of the organic compound.

  Moreover, as a method for cooling the organic compound after heating, a method of natural cooling at room temperature may be used, or a cooling medium may be used to rapidly or forcibly cool the organic compound.

On the other hand, the hydrogen condition is not particularly limited as long as hydrogen is in a gaseous state, and may be in a normal temperature, high temperature, or low temperature state. Moreover, there is no restriction | limiting in particular also about the pressure conditions of hydrogen gas, However, It is preferable that it is 1.0 * 10 < ^-10 > -200MPa, Especially 0.1-70MPa.

  Moreover, there is no restriction | limiting in particular about the time which an organic compound and hydrogen gas contact at high temperature, However, It is preferable to set it as about 0.01 to 24 hours from surfaces, such as working efficiency. Furthermore, it is preferable to set it as about 1 to 7 days about the period left to cool after that.

  In the methods of claim 1 and claim 2, the hydrogen gas to be contacted with the organic compound is preferably a high-purity hydrogen gas. However, as will be described later, when a host compound having a hydrogen selective inclusion ability is used. Alternatively, a mixed gas of hydrogen gas and another gas may be used.

  The hydrogen clathrate compound thus obtained differs depending on the type of host compound used, the contact conditions with hydrogen, etc., but usually clathrates 0.1 to 20 moles of hydrogen molecule per mole of host compound. It is a hydrogen clathrate compound.

  Such a hydrogen clathrate compound stably clathrates hydrogen for a long time at room temperature and normal pressure. In addition, this hydrogen clathrate compound is lighter and easier to handle than hydrogen storage alloys, and is solid, so it can be easily stored and transported in a glass, metal, plastic, or other container. .

  According to the method of the present invention, as a method of extracting hydrogen from a state in which hydrogen is stored, when stored in a hydrogen pressurized state, the hydrogen can be extracted by reducing the pressure state and heated. But you can take it out. Furthermore, stored hydrogen can also be taken out by performing heating and pressure reduction simultaneously.

In particular, in order to release hydrogen from the aforementioned hydrogen clathrate compound, depending on the type of the host compound, the pressure is reduced to about 1.0 × 10 ^{−2 to} 1.0 × 10 ⁻⁵ MPa from normal pressure or normal pressure. Then, it may be heated to about 30 to 200 ° C., particularly about 40 to 100 ° C., whereby hydrogen can be easily released from the hydrogen clathrate compound and used for various applications.

  The host compound after releasing hydrogen from the hydrogen clathrate compound has a selective clathrate ability of hydrogen and can be effectively reused. Accordingly, by using an organic compound having a hydrogen storage history in which hydrogen is stored in an organic compound by the method of the present invention, and then storage and release operations are performed once or twice or more. By bringing hydrogen into contact with normal pressure or pressurized pressure, hydrogen can be easily and efficiently stored again.

  Hereinafter, the present invention will be described more specifically with reference to Examples and Comparative Examples.

  In the following, 1,1-bis (4-hydroxyphenyl) cyclohexane (hereinafter abbreviated as “BHC”) was used as the organic compound for storing hydrogen. The result of measuring this BHC in the temperature range of room temperature to 250 ° C. with a TG-DTA apparatus (temperature increase rate: 10 ° C./min) is as shown in FIG. As the hydrogen, commercially available high-purity hydrogen of 99.99% or more was used.

Example 1
A simple test apparatus in which a glass container (capacity 100 ml) 1 to which a hydrogen vent pipe 2 is attached as shown in FIG. 1 is placed on a hot plate 3 is used, and an organic compound (BHC) 4 is added to the container 1 approximately. 0.5 g was added, and the bottom of the container 1 was heated by the hot plate 3 while hydrogen was vented through the vent pipe 2 at 200 ml / min.

  When the temperature reached 200 ° C., BHC gradually began to vaporize, contacted with hydrogen in a gaseous state, and was carried upwards mixed with a hydrogen stream. Since the temperature of the BHC carried upward decreases, the solid substance 5 was obtained by solidifying and adhering again on the inner wall surface near the opening above the container 1.

  As a result of measuring the obtained solid substance 5 in a temperature range of room temperature to 250 ° C. with a TG-DTA apparatus (heating rate: 10 ° C./min), the solid material 5 was solid at room temperature to about 80 ° C. as shown in FIG. The release component was found to be 2.45% by weight based on the weight of the material.

  On the other hand, in the TG-DTA analysis result of BHC before being brought into contact with hydrogen, as shown in FIG. 2, no release component is observed between room temperature and 80 ° C.

  From the above results, BHC can take hydrogen by contacting with hydrogen in a gaseous state, and can store hydrogen in the obtained solid substance under normal temperature and pressure conditions. It was found that hydrogen can be released by heating the particulate material.

Example 2
1 L of tedra bag having a capacity of 1 L was charged with 1 L of hydrogen and 0.1 g of BHC and sealed, and this tedra bag was left in a constant temperature bath at 100 ° C. for 30 minutes. After heating, the tedra bag was taken out at room temperature (about 20 ° C.) and left for 3 days.

  As a result of measuring the obtained reactant in a temperature range from room temperature to 250 ° C. with a TG-DTA apparatus (temperature increase rate: 10 ° C./min), as shown in FIG. The release component was found to be 0.4% by weight with respect to the weight of.

  On the other hand, the TG-DTA analysis result of BHC before heating with hydrogen shows no release component at room temperature to 100 ° C. as shown in FIG.

  From the above results, BHC can take in hydrogen by contacting with hydrogen in a heated state, and can store hydrogen in the obtained solid substance under normal temperature and normal pressure conditions. It was found that hydrogen can be released by heating the particulate material.

Comparative Example 1
In Example 2, except that no heating was performed, the tedra bag into which hydrogen and BHC were added was left at room temperature (about 20 ° C.), then BHC was taken out and TG-DTA measurement was performed. As shown in Fig. 4, it was found that almost no release component was observed.

1 is a schematic cross-sectional view showing a configuration of a test apparatus used in Example 1. FIG. It is a TG-DTA measurement chart of BHC before contacting with hydrogen. In Example 1, it is a TG-DTA measurement chart of the solid substance obtained by reaction of hydrogen and BHC. In Example 2, it is a TG-DTA measurement chart of BHC after contacting with hydrogen. In the comparative example 1, it is a TG-DTA measurement chart of BHC after contacting with hydrogen.

DESCRIPTION OF SYMBOLS 1 Container 2 Vent pipe 3 Hotplate 4 Organic compound 5 Solid substance

Claims (4)

A hydrogen storage method for bringing hydrogen into a solid substance obtained by bringing an organic compound brought into a gaseous state into contact with hydrogen gas and then cooling, wherein the organic compound is in contact with hydrogen gas to form hydrogen molecules. The hydrogen molecule compound is a hydrogen clathrate compound using the organic compound as a host compound, and the organic compound is urea, 1,1,6,6-tetraphenylhexa-2, 4-diyne-1,6-diol, 1,1-bis (2,4-dimethylphenyl) -2-propyn-1-ol, 1,1,4,4-tetraphenyl-2-butyne-1,4 -Diol, 1,1,6,6-tetrakis (2,4-dimethylphenyl) -2,4-hexadiyne-1,6-diol, 9,10-diphenyl-9,10-dihydroanthracene-9,10- Gio 9,10-bis (4-methylphenyl) -9,10-dihydroanthracene-9,10-diol, 1,1,2,2-tetraphenylethane-1,2-diol, 4-methoxyphenol, 2, , 4-dihydroxybenzophenone, 4,4′-dihydroxybenzophenone, 2,2′-dihydroxybenzophenone, 2,2 ′, 4,4′-tetrahydroxybenzophenone, 1,1-bis (4-hydroxyphenyl) cyclohexane, 4, , 4′-sulfonylbisphenol, 2,2′-methylenebis (4-methyl-6-tert-butylphenol), 4,4′-ethylidenebisphenol, 4,4′-thiobis (3-methyl-6-tert-butylphenol) 1,1,3-tris (2-methyl-4-hydroxy-5-tert-butylphenyl) butane, 1,1,2 , 2-tetrakis (4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethylene, 1,1,2,2-tetrakis (3-methyl-4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (3-fluoro-4-hydroxyphenyl) ethane, α, α, α ′, α′-tetrakis (4-hydroxyphenyl) -p-xylene, tetrakis (p-methoxyphenyl) Ethylene, 3,6,3 ′, 6′-tetramethoxy-9,9′-bi-9H-xanthene, 3,6,3 ′, 6′-tetraacetoxy-9,9′-bi-9H-xanthene, 3,6,3 ′, 6′-tetrahydroxy-9,9′-bi-9H-xanthene, gallic acid, methyl gallate, catechin, bis-β-naphthol, α, α, α ′, α′-tetra Phenyl-1,1'-bifu Nyl-2,2′-dimethanol, diphenic acid bisdicyclohexylamide, fumaric acid bisdicyclohexylamide, cholic acid, deoxycholic acid, 1,1,2,2-tetraphenylethane, tetrakis (p-iodophenyl) ethylene, 9,9′-bianthryl, 1,1,2,2-tetrakis (4-carboxyphenyl) ethane, 1,1,2,2-tetrakis (3-carboxyphenyl) ethane, acetylenedicarboxylic acid, 2,4,5 -Triphenylimidazole, 1,2,4,5-tetraphenylimidazole, 2-phenylphenanthro [9,10-d] imidazole, 2- (o-cyanophenyl) phenanthro [9,10-d] imidazole, 2- (m-cyanophenyl) phenanthro [9,10-d] imidazole, 2- (p-cyano Enyl) phenanthro [9,10-d] imidazole, hydroquinone, 2-t-butylhydroquinone, 2,5-di-t-butylhydroquinone, and 2,5-bis (2,4-dimethylphenyl) hydroquinone A hydrogen storage method characterized by being one or more selected from the group consisting of: A hydrogen storage method in which hydrogen is taken into an organic compound by heating a solid organic compound in a hydrogen gas atmosphere and then cooling, wherein the organic compound is brought into contact with hydrogen gas to form a hydrogen molecular compound. The hydrogen molecule compound is a hydrogen clathrate compound using the organic compound as a host compound, and the organic compound is urea, 1,1,6,6-tetraphenylhexa-2,4- Diin-1,6-diol, 1,1-bis (2,4-dimethylphenyl) -2-propyn-1-ol, 1,1,4,4-tetraphenyl-2-butyne-1,4-diol 1,1,6,6-tetrakis (2,4-dimethylphenyl) -2,4-hexadiyne-1,6-diol, 9,10-diphenyl-9,10-dihydroanthracene-9,10-dio 9,10-bis (4-methylphenyl) -9,10-dihydroanthracene-9,10-diol, 1,1,2,2-tetraphenylethane-1,2-diol, 4-methoxyphenol, 2,4-dihydroxybenzophenone, 4,4′-dihydroxybenzophenone, 2,2′-dihydroxybenzophenone, 2,2 ′, 4,4′-tetrahydroxybenzophenone, 1,1-bis (4-hydroxyphenyl) cyclohexane, 4,4′-sulfonylbisphenol, 2,2′-methylenebis (4-methyl-6-tert-butylphenol), 4,4′-ethylidenebisphenol, 4,4′-thiobis (3-methyl-6-tert-butylphenol) ), 1,1,3-tris (2-methyl-4-hydroxy-5-t-butylphenyl) butane, 1,1, 2,2-tetrakis (4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethylene, 1,1,2,2-tetrakis (3-methyl-4-hydroxyphenyl) ethane 1,1,2,2-tetrakis (3-fluoro-4-hydroxyphenyl) ethane, α, α, α ′, α′-tetrakis (4-hydroxyphenyl) -p-xylene, tetrakis (p-methoxyphenyl) ) Ethylene, 3,6,3 ′, 6′-tetramethoxy-9,9′-bi-9H-xanthene, 3,6,3 ′, 6′-tetraacetoxy-9,9′-bi-9H-xanthene 3,6,3 ′, 6′-tetrahydroxy-9,9′-bi-9H-xanthene, gallic acid, methyl gallate, catechin, bis-β-naphthol, α, α, α ′, α′- Tetraphenyl-1,1'-bi Phenyl-2,2′-dimethanol, diphenic acid bisdicyclohexylamide, fumaric acid bisdicyclohexylamide, cholic acid, deoxycholic acid, 1,1,2,2-tetraphenylethane, tetrakis (p-iodophenyl) ethylene, 9,9′-bianthryl, 1,1,2,2-tetrakis (4-carboxyphenyl) ethane, 1,1,2,2-tetrakis (3-carboxyphenyl) ethane, acetylenedicarboxylic acid, 2,4,5 -Triphenylimidazole, 1,2,4,5-tetraphenylimidazole, 2-phenylphenanthro [9,10-d] imidazole, 2- (o-cyanophenyl) phenanthro [9,10-d] imidazole, 2- (m-cyanophenyl) phenanthro [9,10-d] imidazole, 2- (p-sia Phenyl) phenanthro [9,10-d] imidazole, hydroquinone, 2-t-butylhydroquinone, 2,5-di-t-butylhydroquinone, and 2,5-bis (2,4-dimethylphenyl) hydroquinone A hydrogen storage method characterized by being one or more selected from the group consisting of:   3. The hydrogen storage method according to claim 2, wherein the organic compound is supported on a porous material. 4. The organic compound according to claim 1, wherein the organic compound is 1,1-bis (4-hydroxyphenyl) cyclohexane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethane, 1,1. , 2,2-tetrakis (4-hydroxyphenyl) ethylene, diphenic acid bis (dicyclohexylamide), fumaric acid bisdicyclohexylamide, and 2- (m-cyanophenyl) phenanthro [9,10-d] imidazole One or two or more selected hydrogen storage methods.

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