JP5033829B2 - Digestion gas deoxygenation method and apparatus - Google Patents

Description

  The present invention relates to a digestion gas deoxygenation method and apparatus for removing oxygen remaining in methane gas (hereinafter referred to as “refined gas”) obtained by purifying digestion gas generated by subjecting organic waste to methane fermentation.

Currently, methane fermentation treatment is frequently used to treat organic waste with relatively high water content. The gas generated by this methane fermentation treatment is usually called “digestion gas”, and the components in the digestion gas are about 60% by volume of methane and about 40% by volume of carbon dioxide. Furthermore, sulfur impurities such as 100 to 3000 ppm of hydrogen sulfide (hereinafter referred to as “H ₂ S”) and about 0.3% by volume of oxygen are also included as trace amounts of impurities. This digestion gas is used as a fuel gas. For example, it is a fuel such as a boiler for producing hot water or steam, such as a gas engine for power generation, a gas turbine, or a fuel cell. In recent years, it is highly desired that this digestion gas be further purified and supplied as city gas. However, in order to refine this digestion gas and use it as city gas, it is necessary to remove sulfur impurities such as H ₂ S and oxygen. Moreover, as a technique for removing the organic sulfur compound and oxygen, for example, a technique described in Patent Document 1 is known.

  The technique for removing the organic sulfur compound and oxygen disclosed in Patent Document 1 is as follows. This technique includes a first catalyst containing palladium in a reactor and a second catalyst containing at least one of molybdenum, nickel, or cobalt, and is heated at 300 to 450 ° C. from methane gas containing an organic sulfur compound and oxygen. The organic sulfur compound and oxygen are removed at the same time.

JP 58-215488 A

However, the technology for removing organic sulfur compounds and oxygen disclosed in Patent Document 1 first converts oxygen that inhibits desulfurization of organic sulfur compounds into water vapor on the first catalyst, and then organic sulfur on the second catalyst. The compound is converted to H ₂ S and has the following problems.

1) In a reaction for converting oxygen into water vapor from a methane gas containing an organic sulfur compound and oxygen, and a reaction for converting an organic sulfur compound into H ₂ S, a high temperature of 300 to 450 ° C. is required.
2) The organic sulfur compound in the gas to be treated is converted to H ₂ S and remains in the gas.

An object of the present invention is to purify digestion gas and remove oxygen remaining in the purified gas without requiring a high temperature, and sulfur-based impurities such as H ₂ S do not remain in the purified gas. It is an object of the present invention to provide a digestion gas deoxygenation method and apparatus.

The invention described in claim 1
The digestion gas generated by subjecting the organic waste to methane fermentation is compressed and compressed by a compressor, the pressurized digestion gas is supplied to an absorption tower, and the digestion gas and water pressurized in the absorption tower are supplied. By contacting in a high pressure state, carbon dioxide and sulfur impurities contained in the pressurized digestion gas are dissolved in high pressure water to separate the carbon dioxide and sulfur impurities from the pressurized digestion gas, thereby purifying methane gas. Process,
Adding hydrogen to the purified methane gas (hereinafter referred to as “purified gas”);
Supplying the purified gas to which the hydrogen has been added to a catalyst tower packed with a catalyst, converting oxygen remaining in the purified gas to which the hydrogen has been added by catalytic reaction into water, and removing the oxygen;
Depressurizing the high-pressure water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved, and the carbon dioxide and water from the water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved. A step of separating sulfur impurities;
Supplying oxygen to the separated carbon dioxide and sulfur impurities;
The separated carbon dioxide and sulfur-based impurities and the newly supplied oxygen are supplied to a biological desulfurization tower having a filler layer to which microorganisms that decompose sulfur-based impurities are attached, and the action of the microorganisms is utilized. Decomposing sulfur impurities in a mixed gas in which the carbon dioxide and sulfur impurities and the newly supplied oxygen are mixed;
A digestion gas deoxygenation method characterized by comprising:

Invention of Claim 2 has the process of cooling the refined gas after the oxygen which remains in the refined gas in the invention of Claim 1 converted into water with a heat exchanger. And

The invention according to claim 3 detects the concentration of at least one of methane, carbon dioxide, and H ₂ S in the purified gas at the absorption tower outlet in the invention according to claim 1 or 2. If the concentration of the detected gas is not within the range of the specified value, the purified gas at the outlet of the absorption tower is bypassed to other than the catalyst tower by a flow path switching valve, and the concentration of the detected gas is within the range of the specified value. In this case, the method has a step of supplying the purified gas at the outlet of the absorption tower to the catalyst tower through the flow path switching valve.

The invention according to claim 4 is the invention according to any one of claims 1 to 3 , wherein the hydrogen and the newly supplied oxygen are obtained by electrolyzing water. Features.

The invention according to claim 5 is the invention according to any one of claims 1 to 4 , wherein the catalyst layer space velocity SV of the purified gas to which the hydrogen supplied to the catalyst tower is added is 7, 000h ⁻¹ or less (however, zero is not included).

The invention according to claim 6 is the invention according to any one of claims 1 to 5 , wherein in the step of adding hydrogen to the purified gas, the amount of hydrogen added is the amount of oxygen remaining in the purified gas. The molar ratio is 2 or more.

The invention described in claim 7
A compressor that compresses and pressurizes digestion gas generated by methane fermentation of organic waste;
The digestion gas and water pressurized by the compressor are received and contacted in a high-pressure state to dissolve carbon dioxide and sulfur impurities contained in the pressurized digestion gas in high-pressure water and from the pressurized digestion gas. An absorption tower for separating carbon dioxide and sulfur impurities and purifying methane gas;
Hydrogen supply means for adding hydrogen to the purified methane gas (hereinafter referred to as “purified gas”);
A catalyst tower that receives a purified gas to which hydrogen has been added by the hydrogen supply means, and is filled with a catalyst that converts and removes oxygen remaining in the purified gas to which hydrogen has been added; and
Depressurizing the high-pressure water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved, and the carbon dioxide and water from the water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved. Separation means for separating sulfur impurities;
Oxygen supply means for supplying new oxygen to the separated carbon dioxide and sulfur impurities;
A biological desulfurization tower having a filler layer to which the separated carbon dioxide and sulfur-based impurities and new oxygen supplied from the oxygen supply means are received and microorganisms that decompose the sulfur-based impurities are attached;
A digestion gas deoxygenation apparatus comprising:

The invention described in claim 8 is characterized in that, in the invention described in claim 7 , a heat exchanger for cooling the purified gas exiting from the catalyst tower is provided at the rear stage of the catalyst tower.

The invention according to claim 9 is the invention according to claim 7 or 8 , wherein methane, carbon dioxide, or H ₂ S in the purified gas at the outlet of the absorption tower is between the absorption tower and the catalyst tower. A detection means for detecting the concentration of at least one gas; and a flow path switching valve provided between the detection means and the catalyst tower, wherein the concentration of the gas detected by the detection means is a specified value. If the concentration of the gas detected by the detection means is within a specified value range, the purified gas at the outlet of the absorption tower is bypassed to other than the catalyst tower by the flow path switching valve. The purified gas at the tower outlet is supplied to the catalyst tower by the flow path switching valve.

The invention described in claim 10 is the invention described in any one of claims 7 to 9 , wherein the hydrogen supply means and the oxygen supply means are water electrolysis devices.

The invention according to claim 11 is the invention according to any one of claims 7 to 10 , wherein the catalyst layer space velocity SV of the purified gas to which the hydrogen supplied to the catalyst tower is added is 7, 000h ⁻¹ or less (however, zero is not included).

The invention according to claim 12 is the invention according to any one of claims 7 to 11 , wherein the amount of hydrogen added by the hydrogen supply means is the molar amount of oxygen remaining in the purified gas. The ratio is 2 or more.

As described above, according to the deoxygenation process of engaging Ru digestion gas present invention,
The digestion gas generated by subjecting the organic waste to methane fermentation is compressed and compressed by a compressor, the pressurized digestion gas is supplied to an absorption tower, and the digestion gas and water pressurized in the absorption tower are supplied. By contacting in a high pressure state, carbon dioxide and sulfur impurities contained in the pressurized digestion gas are dissolved in high pressure water to separate the carbon dioxide and sulfur impurities from the pressurized digestion gas, thereby purifying methane gas. Process,
Adding hydrogen to the purified methane gas (hereinafter referred to as “purified gas”);
Supplying the purified gas to which the hydrogen has been added to a catalyst tower packed with a catalyst, converting oxygen remaining in the purified gas to which the hydrogen has been added by catalytic reaction into water, and removing the oxygen;
Depressurizing the high-pressure water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved, and the carbon dioxide and water from the water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved. A step of separating sulfur impurities;
Supplying oxygen to the separated carbon dioxide and sulfur impurities;
The separated carbon dioxide and sulfur-based impurities and the newly supplied oxygen are supplied to a biological desulfurization tower having a filler layer to which microorganisms that decompose sulfur-based impurities are attached, and the action of the microorganisms is utilized. Decomposing sulfur impurities in a gas in which the carbon dioxide and sulfur impurities and the newly supplied oxygen are mixed;
Therefore, the following effects are achieved.
1) hardly exists methane gas in the high-pressure water withdrawn from the absorption Osamuto, since contrary to most of the carbon dioxide and sulfur-based impurities digestion gas is present in the high-pressure water, vacuum high pressure water Thus, the optimum desulfurization can be realized by appropriately adding oxygen according to the amount of H ₂ S contained in the gas without worrying about preventing the explosion of the gas containing carbon dioxide and sulfur impurities generated.
2) In addition, as described in the above 1), the gas containing carbon dioxide, sulfur impurities and oxygen supplied to the biological desulfurization tower contains almost no methane gas, so sulfur impurities such as H ₂ S. Desulfurization with a compact biological desulfurization tower as a removal treatment section can be realized.
Furthermore, according to the method of Claim 4, there exist the following effects.
1) Since hydrogen obtained by electrolysis of water has high purity, there is little mixing of impurities, and the purity of the purified gas can be easily maintained.
2) Moreover, since the oxygen obtained by electrolysis is also highly pure, compared with the case where air is used as an oxygen source for biological desulfurization, the biological desulfurization tower as a removal treatment section for sulfur impurities such as H ₂ S. Desulfurization with a more compact can be realized.
3) When hydrogen is stored in a hydrogen high-pressure vessel (cylinder, etc.), handling of high-pressure hydrogen becomes complicated, whereas hydrogen production by electrolysis does not require storage of high-pressure hydrogen and is safe. high.
4) It is also possible to adjust the hydrogen addition amount by detecting the concentration and controlling the current with respect to the fluctuation of the oxygen concentration in the purified gas.

Further, according to the deoxygenator engagement Ru digestion gas present invention,
A compressor that compresses and pressurizes digestion gas generated by methane fermentation of organic waste;
The digestion gas and water pressurized by the compressor are received and contacted in a high-pressure state to dissolve carbon dioxide and sulfur impurities contained in the pressurized digestion gas in high-pressure water and from the pressurized digestion gas. An absorption tower for separating carbon dioxide and sulfur impurities and purifying methane gas;
Hydrogen supply means for adding hydrogen to the purified methane gas (hereinafter referred to as “purified gas”);
A catalyst tower that receives a purified gas to which hydrogen has been added by the hydrogen supply means, and is filled with a catalyst that converts and removes oxygen remaining in the purified gas to which hydrogen has been added; and
Depressurizing the high-pressure water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved, and the carbon dioxide and water from the water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved. Separation means for separating sulfur impurities;
Oxygen supply means for supplying new oxygen to the separated carbon dioxide and sulfur impurities;
A biological desulfurization tower having a filler layer to which the separated carbon dioxide and sulfur-based impurities and new oxygen supplied from the oxygen supply means are received and microorganisms that decompose the sulfur-based impurities are attached;
Therefore, the following effects are achieved.
1) hardly exists methane gas in the high-pressure water withdrawn from the absorption Osamuto, since contrary to most of the carbon dioxide and sulfur-based impurities digestion gas is present in the high-pressure water, vacuum high pressure water Thus, the optimum desulfurization can be realized by appropriately adding oxygen according to the amount of H ₂ S contained in the gas without worrying about preventing the explosion of the gas containing carbon dioxide and sulfur impurities generated.
2) In addition, as described in the above 1), the gas containing carbon dioxide, sulfur impurities and oxygen supplied to the biological desulfurization tower contains almost no methane gas, so sulfur impurities such as H ₂ S. It is also possible to realize a desulfurization section in which the biological desulfurization tower as the removal treatment section is made compact.
Furthermore, according to the apparatus of Claim 10, there exist the following effects.
1) Since hydrogen obtained by electrolysis of water has high purity, there is little mixing of impurities, and the purity of the purified gas can be easily maintained.
2) Moreover, since the oxygen obtained by electrolysis is also highly pure, compared with the case where air is used as an oxygen source for biological desulfurization, the biological desulfurization tower as a removal treatment section for sulfur impurities such as H ₂ S. Desulfurization with a more compact can be realized.
3) When hydrogen is stored in a hydrogen high-pressure vessel (cylinder, etc.), handling of high-pressure hydrogen becomes complicated, whereas hydrogen production by electrolysis does not require storage of high-pressure hydrogen and is safe. high.
4) It is also possible to adjust the hydrogen addition amount by detecting the concentration and controlling the current with respect to the fluctuation of the oxygen concentration in the purified gas.

It is explanatory drawing which illustrates typically the whole structure of the deoxidation apparatus of the digestive gas of Embodiment 1 of this invention. It is explanatory drawing which illustrates typically the whole structure of the deoxidation apparatus of the digestive gas of Embodiment 2 of this invention. It is explanatory drawing which illustrates typically the whole structure of the deoxidation apparatus of the digestive gas of Embodiment 3 of this invention. It is explanatory drawing which illustrates typically the whole structure of the deoxidation apparatus of the digestive gas of Embodiment 4 of this invention.

  Embodiments of the present invention will be described below with reference to the accompanying drawings.

(Embodiment 1)
FIG. 1 is an explanatory diagram schematically illustrating the overall configuration of a digestion gas deoxygenation apparatus according to Embodiment 1 for carrying out the digestion gas deoxygenation method of the present invention.

  In FIG. 1, 1 is a mist separator, 2a and 2b are gas compressors, 3 is an absorption tower (scrubber), 4 is a water supply tank, 5 is a water supply pump, 6 is a water electrolysis device as hydrogen supply means, and 7 is Palladium (Pd) catalyst, 8 is a catalyst tower packed with Pd catalyst 7, and 9 is a dehumidifier.

  Next, the operation of the digestion gas deoxygenation apparatus according to the present invention will be described with reference to FIG.

Digestion gas generated by methane fermentation of organic waste such as organic sludge and organic wastewater is removed by mist separator 1 from mist (water) and dust. The components in the digestion gas after passing through the mist separator 1 are about 60% by volume of methane, about 40% by volume of carbon dioxide, about 0.3% by volume of oxygen, and 100 to 100% of H ₂ S as a sulfur impurity. 3000 ppm, other impurities are very small. The digestion gas is compressed by gas compressors 2a and 2b connected in series, and the pressure is increased to a predetermined pressure higher than the atmospheric pressure. The digestion gas pressurized by the gas compressors 2 a and 2 b is introduced into the lower part of the absorption tower 3. On the other hand, from the upper part of the absorption tower 3, it is pumped up by a water supply pump 5 from a water supply tank 4 in which sand filtrate from a sand filtration facility of treated water provided downstream of the final sedimentation basin of the sewage treatment plant is stored. And is supplied in a boosted state. As water used at this time, in addition to using sand filtration water from the sand filtration facility of the treated water provided downstream of the final sedimentation basin of the sewage treatment plant, tap water, well water, or It is also possible to use treated water obtained by treating wastewater such as sewage.

  As described above, the digestion gas is pressurized by the gas compressors 2a and 2b and fed into the absorption tower 3 from the lower part thereof, and the water is boosted by the water replenishment pump 5 and fed into the absorption tower 3 from the upper part thereof. The inside of the absorption tower 3 is kept in a high pressure state satisfying the range of 0.55 to 2.0 MPaG, and the digestion gas and water are brought into contact with each other in the high pressure state satisfying the pressure range in the absorption tower 3. The absorption tower 3 is filled with a packing such as Raschig ring in order to bring the digestion gas and water into sufficient contact.

Sulfur such as carbon dioxide and H ₂ S contained in the digestion gas in a gaseous state by bringing the digestion gas and water into contact with each other at a high pressure satisfying the range of 0.55 to 2.0 MPaG in the absorption tower 3. System impurities are dissolved and absorbed in high-pressure water, while methane gas is taken out from the top of the absorption tower 3 with almost no dissolution in high-pressure water. Further, when purifying methane gas by separating sulfur-based impurities such as carbon dioxide and H ₂ S from the digestion gas, the digestion gas and water are brought into contact in a high pressure state satisfying the range of 0.55 to 2.0 MPaG. Good. The low pressure atmosphere than this range, not carbon dioxide and H _{2 S} sulfur based impurities are sufficiently separated and removed, such as, also, the sulfur-based impurities such as carbon dioxide and H _{2 S} even in the high pressure atmosphere from this range The removal rate is not improved so much, which is not preferable from the viewpoints of operation cost and increase in apparatus cost due to high pressure specifications. In addition, it is more preferable to make digestion gas and water contact in the high pressure state which satisfy | fills the range of 0.7 MPaG or more and less than 1.0 MPaG from the point of a removal rate, an operating cost, and apparatus cost.

In addition, when a siloxane compound is contained in the digestion gas by contacting the digestion gas and water in a high pressure state of 0.55 MPaG or more as described above, the siloxane compound is condensed and separated from the digestion gas. A small amount of siloxane compound remains in the purified gas having a high concentration of methane gas taken out from the top of the absorption tower 3. However, since about 0.3% by volume of oxygen still remains in this purified gas, it cannot be used as city gas as it is. Then, hydrogen (H ₂ ) is added from the water electrolysis device 6 to this purified gas (mainly high-concentration methane gas and the above-mentioned oxygen content), and the purified gas to which this hydrogen is added is filled with the Pd catalyst 7. By feeding into the catalyst tower 8, a catalytic reaction as shown in the following formula (1) proceeds at room temperature, and oxygen (O ₂ ) in the purified gas is removed to, for example, 0.01% by volume or less. .
O ₂ + 2H ₂ → 2H ₂ O ――― Formula (1)

  From the above reaction formula (1), hydrogen needs to have a molar amount twice that of oxygen. Therefore, it is possible to control the oxygen remaining in the purified gas to 0.01% by volume or less by adding hydrogen in a molar ratio of 2 or more with respect to oxygen. The amount of hydrogen added to oxygen is preferably 2 to about 3.3 in molar ratio. Thereby, it is possible to prevent excessive consumption of hydrogen while removing remaining oxygen to a predetermined reference value or less.

The Pd catalyst 7-layer space velocity (SV) of the purified gas to which hydrogen is added can be changed within a range of 7,000 h ⁻¹ or less (excluding zero), preferably 3,000. It is in the range of ˜6,000 h ⁻¹ . As a result, the amount of Pd catalyst 7 to be used is not unnecessarily increased while removing the remaining oxygen to a predetermined reference value or less. Therefore, the size of the catalyst tower 8 can be suppressed.

The purified gas with reduced oxygen is sent to the dehumidifier 9 and the moisture is sufficiently absorbed and removed, and then connected to the city gas conduit. Moreover, the high pressure water in which sulfur impurities such as carbon dioxide and H ₂ S separated from the digestion gas are dissolved is extracted from the bottom of the absorption tower 3 and supplied to the water treatment facility via the valve V1. As the dehumidifier 9, an adsorption tower using an adsorbent such as molecular sieve can be applied.

Since it is the above structures, in the digestion gas deoxygenation method and apparatus which concern on this invention, there exist the following effects.
1) Since there is a step of previously separating carbon dioxide and sulfur-based impurities in digestion gas using a high-pressure water absorption method and purifying methane gas, it is not necessary to remove sulfur-based impurities and oxygen at the same time. Therefore, when removing oxygen remaining in the purified gas, a method that does not require a high temperature of 300 to 450 ° C. for the catalytic reaction, and can be sufficiently deoxygenated simply by adding hydrogen and proceeding the catalytic reaction at room temperature. realizable.
2) In addition, when the above catalytic reaction is started at room temperature and oxygen is converted to water, the temperature rises to about 100 ° C. due to the heat of reaction, so that the water remains as steam and does not condense in the catalyst tower, Water as a liquid does not adhere to the catalyst in the catalyst tower, and the efficiency of the catalytic reaction does not decrease.
3) In addition, since a very small amount of sulfur-based impurities such as H ₂ S remaining in the methane gas purified by the high-pressure water absorption method is dissolved in water, this very small amount of sulfur-based impurities such as H ₂ S is also present. It can be separated from the purified gas.
4) Moreover, since hydrogen obtained by electrolysis of water has high purity, there is little mixing of impurities, and the purity of the purified gas can be easily maintained.

  The water electrolysis device 6 in the present embodiment can be used as long as it generates hydrogen, and a preferable water electrolysis device includes a water electrolysis hydrogen generation device using a solid polymer electrolyte membrane or the like. It is possible to use a water electrolysis type high purity hydrogen oxygen generator (trade name: HHOG) manufactured by Shinko Environmental Solution Co., Ltd., which generates high purity hydrogen and oxygen. By using this water electrolysis-type high-purity hydrogen oxygen generator, it is not necessary to store hydrogen in advance using a high-pressure hydrogen cylinder, and high-purity hydrogen is required when the power is turned on / off. It is safe to supply only a small amount. Further, it is possible to control the amount of hydrogen by detecting the concentration with respect to fluctuations in the oxygen concentration in the purified gas. Thus, it is possible to control the amount of oxygen remaining in the purified gas. Further, as described later, high-purity oxygen can be supplied at the same time.

  Further, in the present embodiment, a coalescer as a mist separator is not shown before and after the catalyst tower 8, but it is preferable to install a coalescer. By doing so, scattered water can be removed. As the Pd catalyst 7, palladium compounds such as metal palladium, palladium oxide, and palladium hydroxide can be used. Further, any catalyst can be used as long as it has an action of promoting the reaction between oxygen and hydrogen at room temperature, such as platinum. Furthermore, those obtained by supporting these catalyst substances on a carrier such as alumina or zeolite can also be used.

In order to confirm the effects of the present invention, the following laboratory tests were conducted. In FIG. 1, for example, a purified gas in which 0.3% by volume of oxygen to which hydrogen is added remains is supplied to the catalyst tower 8 to advance the catalytic reaction, and the oxygen concentration in the purified gas exiting the catalyst tower 8 is 50 ppm. A test was conducted to find out how much the SV value could be less than (target value: a value that is sufficiently satisfactory even when used as city gas). Since the purified gas when the digestion gas is purified using the absorption tower 3 contains moisture, the test gas is composed of 0.3 vol% oxygen concentration, 0.6 vol% hydrogen concentration, and the remaining methane gas Water was supplied to the gas to be 30 ° C. saturated water content (see Table 1 below). As test conditions, when the SV value ^{3,000h -1, 5,000h -1,} and three levels of 7,000H ^-1, as the feed water was respectively 12μL / min, 21μL / min, and 29 [mu] L / min ( See Table 1 below). In addition, the pressures of the above three levels of test gases (test Nos. 1, 2, and 3) are all 0.9 MPaG (see Table 1 below). These three levels of test gas (test Nos. 1, 2, and 3) were supplied to the catalyst tower 8, and the test no. The oxygen concentration and hydrogen concentration in the test gases 1, 2, and 3 were measured every 1 hour until the total elapsed time reached 6 hours. In addition, after 6 hours, the test No. 1 exiting the catalyst tower 8 occurred. The accumulated moisture content in the test gases 1, 2, and 3 was also measured, and the moisture content converted per unit time was determined (the results are shown in Table 1 below).

As shown in Table 1 above, Test No. 1, 2, and 3 (that is, the SV values are 3,000 h ⁻¹ , 5,000 h ⁻¹ , and 7,000 h ⁻¹ ) in the test gas exiting the catalyst tower 8 until 6 hours have elapsed. The oxygen concentration was 0 ppm, which was less than the target value of 50 ppm (indicated in parentheses). As described above, since the oxygen concentration in the test gas exiting the catalyst tower 8 can be sufficiently less than the target value of 50 ppm even when the SV value = 7,000 h ⁻¹ , oxygen added with hydrogen even in actual operation. This is also a proof that the amount of Pd catalyst 7 to be used does not become unnecessarily large when oxygen is removed from the 0.3% by volume remaining purified gas. That is, it is suggested that the size of the catalyst tower 8 can be suppressed.

In addition, as shown in Table 1 above, Test No. 1, 2, and 3 (that is, the SV values are 3,000 h ⁻¹ , 5,000 h ⁻¹ , and 7,000 h ⁻¹ ) in the test gas exiting the catalyst tower 8 until 6 hours have elapsed. The hydrogen concentration of was also 0 ppm, satisfying the target value of less than 50 ppm. This is proof that the amount of hydrogen added to oxygen in the purified gas can be made 2 in molar ratio even in actual operation. Therefore, consumption of hydrogen more than necessary can be prevented.

In addition, as shown in Table 1 above, Test No. Per unit time contained in the test gas exiting the catalyst tower 8 at ¹ , 2, and 3 (that is, SV levels of 3,000 h ⁻¹ , 5,000 h ⁻¹ and 7,000 h ⁻¹ ). The converted water amounts were 1.5062 g / h (water recovery rate: 87%), 2.5552 g / h (water recovery rate: 90%), 3.6302 g / h (water recovery rate: 91%), respectively. It was. This is also evidence that an appropriate catalytic reaction corresponding to the SV value has occurred in order to make the oxygen concentration in the test gas exiting the catalyst tower 8 less than the target value of 50 ppm.

(Embodiment 2)
FIG. 2 is an explanatory diagram schematically illustrating the overall configuration of a digestion gas deoxygenation apparatus according to Embodiment 2 for carrying out the digestion gas deoxygenation method of the present invention. In the present embodiment, the same components as those in the first embodiment are given the same numbers, and detailed description thereof is omitted, and only different portions are described in detail.

  In FIG. 2, 20 is a heat exchanger. In the present embodiment, a portion that is greatly different from the first embodiment is that a heat exchanger 20 is installed between the catalyst tower 8 and the dehumidifier 9, and therefore this portion will be described in detail.

  When the deoxygenation reaction proceeds due to the catalytic reaction in the catalyst tower 8, the temperature of the purified gas containing the water exiting the catalyst tower 8 is increased by the heat of reaction. By cooling the purified gas containing moisture whose temperature has been increased by the heat exchanger 20 and lowering the temperature, the moisture adsorption capacity of the dehumidifier 9 in the subsequent stage is increased. Thus, when the moisture adsorption capacity in the dehumidifier 9 is increased, the dehumidifier 9 can be made compact. Further, by reducing the temperature of the purified gas containing the water that has exited the catalyst tower 8, a part of the water in the purified gas is condensed, and the condensed water is provided in a drain trap (see FIG. Since the amount of water in the purified gas introduced into the dehumidifier 9 is also reduced by separating it at a not-shown) and discharging it out of the system, the dehumidifier 9 can be made more compact. In the case where the purified gas with the increased amount of remaining oxygen is deoxygenated by the catalyst tower 8, the amount of heat of reaction becomes higher, so the role played by this configuration (the configuration in which the heat exchanger 20 is added) becomes more important. . In addition, by cooling the purified gas temperature at the outlet of the heat exchanger 20 to be lower than the purified gas temperature at the outlet of the absorption tower 3, more moisture than the moisture generated by the catalytic reaction can be condensed, and the dehumidifier This contributes to further downsizing of 9, which is preferable.

  In the present embodiment, a coalescer as a mist separator is not shown in front of the catalyst tower 8, but it is preferable to install a coalescer. By doing so, scattered water can be removed.

(Embodiment 3)
FIG. 3 is an explanatory view schematically illustrating the overall configuration of a digestion gas deoxygenation apparatus according to Embodiment 3 for carrying out the digestion gas deoxygenation method of the present invention. In the present embodiment, the same components as those in the first embodiment are given the same numbers, and detailed description thereof is omitted, and only different portions are described in detail.

In FIG. 3, 30 is a detection means for detecting the concentration of at least one of methane, carbon dioxide, and H ₂ S, and 40 is a flow path switching valve. In the present embodiment, the part greatly different from the first embodiment is that the detection means 30 for detecting the concentration of at least one of methane, carbon dioxide, and H ₂ S at the outlet of the absorption tower 3 is provided. When the gas concentration that is installed and detected by the detection means 30 is not within the range of the specified value, the gas at the outlet of the absorption tower 3 is bypassed by the flow path switching valve 40 and returned to the mist separator 1. It is a point. Therefore, this part will be described in detail.

At the start of operation of the absorption tower 3, the pressure in the absorption tower 3 has not yet increased, so water cannot be supplied from the upper part of the absorption tower 3 by the water supply pump 5. Therefore, the digestion gas with carbon dioxide and H ₂ S (or siloxane compound depending on the case) remaining from the outlet of the absorption tower 3 comes out. Therefore, if such digested gas with carbon dioxide and H ₂ S (or siloxane compound in some cases) remaining is supplied to the catalyst tower 8 as it is, the catalyst will be deteriorated. However, in the case of having the above-described configuration, if the concentration of the gas detected by the detection means 30 is not within the specified value range, the purified gas at the outlet of the absorption tower 3 (however, the detection means 30 When the concentration of the detected gas is not within the range of the specified value, it is not a purified gas having a predetermined composition, but a digestion gas in which carbon dioxide and H ₂ S (or a siloxane compound in some cases) remain. } Is bypassed by the flow path switching valve 40 and is not supplied to the catalyst tower 8, so that the deterioration of the catalyst can be prevented.

In the present embodiment, the configuration shown in the first embodiment includes the detection means 30 and the flow path switching valve 40 for detecting the concentration of at least one of methane, carbon dioxide, and H ₂ S. Although the example added to is described, it is not necessarily limited to this, and it is naturally possible to add to the configuration shown in the second embodiment.

In the present embodiment, when the concentration of the gas detected by the detection means 30 is not within the range of the specified value, the purified gas at the outlet of the absorption tower 3 (however, the concentration of the gas detected by the detection means 30) Is not in the range of the specified value, it is not a purified gas having a predetermined composition, but carbon dioxide, H ₂ S (or, in some cases, a siloxane compound) remains as a digestion gas}. Although an example in which it is bypassed at 40 and returned to the mist separator 1 has been described, this is only an example and is not necessarily limited thereto.

(Embodiment 4)
FIG. 4 is an explanatory view schematically illustrating the overall configuration of a digestion gas deoxygenation apparatus according to Embodiment 4 for carrying out the digestion gas deoxygenation method of the present invention. In the present embodiment, the same components as those in the first embodiment are given the same numbers, and detailed description thereof is omitted, and only different portions are described in detail. In FIG. 4, 10 is a water circulation pump, 11 is a heat exchanger, 12 is a chiller, 13 is a decompression tank (flushing tank), 14 is a stripping tower (stripping tower), and 15 is mainly a bacterium belonging to the genus Thiobacillus. A filler layer to which aerobic sulfur-oxidizing bacteria are attached, 16 is a biological desulfurization tower containing the filler layer 15, and 17 is a concentration of H ₂ S as a sulfur-based impurity in the digested gas that has passed through the mist separator 1. H ₂ S densitometer.

In the present embodiment, the part greatly different from that of the first embodiment is the high-pressure water treatment process after separating sulfur-based impurities such as carbon dioxide and H ₂ S from digestion gas using the high-pressure water absorption method. (In particular, a desulfurization step is added), so this part will be described in detail. Further, in the present embodiment, unlike the case of the first embodiment, the water is not boosted by the water replenishment pump 5 and fed from the upper part of the absorption tower 3, but is boosted by the water circulation pump 10 as will be described later. The circulating water thus supplied is supplied from the upper part of the absorption tower 3.

In FIG. 4, high-pressure water in which sulfur impurities such as carbon dioxide and H ₂ S separated from digestion gas are dissolved is extracted from the bottom of the absorption tower 3 and introduced into the vacuum tank 13 through the valve V1. . The pressure in the decompression tank 13 is reduced compared to that in the absorption tower 3. For example, when the pressure in the absorption tower 3 is 0.9 MPaG, the pressure in the decompression tank 13 is 0.3 MPaG. For the purpose of increasing the recovery rate of methane gas, the methane gas slightly dissolved in the high-pressure water from the bottom of the absorption tower 3 is separated and gas compressors 2a, 2b are passed from the top of the decompression tank 13 through the valve V2. It is returned to the intermediate stage of the gas and is joined to the digestion gas from the gas compressor 2a. The water in which sulfur impurities such as carbon dioxide and H ₂ S are dissolved after the methane gas is separated and recovered is introduced from the bottom of the decompression tank 13 to the upper portion of the diffusion tower 14 through the valve V3. Further, as described in the first embodiment, the water generated in the deoxygenation process in the catalyst tower 8 (however, this water remains as steam due to the catalytic reaction heat and does not condense in the catalyst tower). The condensed water is recovered as condensed water by a drain trap (not shown) between the catalyst tower 8 and the dehumidifier, and sulfur-based impurities such as H ₂ S remaining in the purified gas in a trace amount are dissolved in the condensed water. Introduced into the separator 1. In addition, by providing a drain trap between the catalyst tower 8 and the dehumidifier, moisture in the deoxygenated purified gas from the catalyst tower 8 is reduced, so that the dehumidifier downstream of the drain trap is prevented from being enlarged. it can. In addition, in this Embodiment, although the example which introduce | transduces the said condensed water into the mist separator 1 was demonstrated, it is not limited to this, It introduce | transduces into the separator of the discharge side of the compressor 2b which is not shown in figure. Is also possible.

In the stripping tower 14, the water extracted from the decompression tank 13 is introduced from the upper part and depressurized to about atmospheric pressure, and new oxygen necessary for biological desulfurization is supplied from the lower part by the water electrolysis device 6. . By reducing the pressure to about atmospheric pressure and by this oxygen, sulfur-based impurities such as carbon dioxide and H ₂ S dissolved in the water extracted from the vacuum tank 13 are separated from the water. The separated sulfur-based impurities such as carbon dioxide and H ₂ S are mixed with new oxygen supplied from the water electrolysis device 6, and the mixed carbon dioxide, sulfur-based impurities such as H ₂ S and new oxygen are mixed. The mixed gas is introduced into the upper part of the biological desulfurization tower 16. Further, the oxygen supply means for supplying new oxygen necessary for biological desulfurization is not necessarily limited to the water electrolysis apparatus 6, but by using the water electrolysis apparatus, a hydrogen supply means and an oxygen supply means. It is preferable because it can serve as both. In addition, as described above, for example, by using a water electrolysis type high-purity hydrogen oxygen generator (trade name: HHOG) manufactured by Shinko Environmental Solution Co., Ltd., high purity oxygen is required by turning the power ON / OFF. You can supply only the amount you need.

Further, the water from which sulfur impurities such as carbon dioxide and H ₂ S have been expelled is extracted from the bottom of the diffusion tower 14, boosted by the water circulation pump 10, and brine from the chiller 12 by the heat exchanger 11. And is cooled to a predetermined temperature (for example, 7 ° C.) and then supplied to the upper portion of the absorption tower 3. The diffusion tower 14 is filled with a packing such as Raschig ring in order to bring the oxygen and water into sufficient contact.

  Moreover, as the water introduced from the upper part of the biological desulfurization tower 16, the water stored in the water tank 4 or the waste water discharged from the valve V4 can be used. Moreover, when using warm water as water introduced from the upper part of the biological desulfurization tower 16, since the action | operation of the sulfur oxidation bacteria in the biological desulfurization tower 16 mentioned later becomes active by providing the following structures, More preferred. For example, hot water (for example, 30 to 50 ° C.) is produced by heat generated from the compressors 2 a and 2 b, and the hot water is introduced from the upper part of the biological desulfurization tower 16. Specifically, water used for cooling the compressors 2 a and 2 b is introduced from the upper part of the biological desulfurization tower 16. Further, it is preferable to recover the heat generated from the compressors 2a and 2b and warm the biological desulfurization tower 16 using the recovered heat. That is, a cooling means (not shown) for cooling the heat generated from the compressors 2a and 2b with water is provided close to the compressors 2a and 2b. And the heat retention means (not shown) provided in the vicinity of the biological desulfurization tower 16 from the recovery means (not shown) which collected the warm water (for example, 50 ° C. to 60 ° C.) after being cooled by the cooling means. The warm water is heated to about 37 ° C. so that the action of sulfur-oxidizing bacteria in the biological desulfurization tower 16 becomes most active.

Next, a process of decomposing (desulfurizing) sulfur-based impurities such as H ₂ S in a mixed gas composed of carbon dioxide, H ₂ S and other sulfur-based impurities and new oxygen in the biological desulfurization tower 16 will be described. By passing the mixed gas and water introduced from the upper part of the biological desulfurization tower 16 through the filler layer 15 to which aerobic sulfur-oxidizing bacteria mainly including Thiobacillus bacteria are attached, the aerobic sulfur-oxidizing bacteria can function. Utilizing it, H ₂ S in sulfur-based impurities is oxidized and decomposed to change to sulfur (S). Further, this S is oxidized and changed to SO ₄ ²⁻ . Through such a process, sulfur-based impurities such as H ₂ S are finally decomposed and removed from the digestion gas (desulfurization is completed).

In the biological desulfurization tower 16, desulfurization is stably performed when the concentration of H ₂ S as a sulfur-based impurity is constant, and the efficiency is improved. Therefore, as in the present embodiment, the following mechanism is used. It is more preferable to provide it. That is, an H ₂ S concentration meter 17 for measuring the concentration of H ₂ S as a sulfur-based impurity in the digestion gas is provided at a location that has passed through the mist separator 1, and in the mixed gas introduced into the biological desulfurization tower 16. the concentration of H _{2 S} in so as to maintain substantially constant, depending on the concentration of the measured H _{2 S,} to control the amount of oxygen supplied from water electrolysis apparatus 6.

In the above desulfurization process, H ₂ S is oxidized and decomposed, and the changed S tends to adhere to the filler layer 15. Therefore, it is more preferable to provide the following mechanism as in this embodiment. That is, the inside of the biological desulfurization tower 16 is filled with bubbles generated by foaming of carbon dioxide and sulfur impurities such as H ₂ S in high pressure water in which sulfur impurities such as carbon dioxide and H ₂ S extracted from the absorption tower 3 are dissolved. In order to wash S adhering to the material layer 15, high-pressure water supply means (not shown) for supplying this high-pressure water to the biological desulfurization tower 16 may be provided. In this way, the deposit is washed with the bubble-containing water generated by foaming from the high-pressure water, and the deposit consisting of peeled S and the like is drained through the valve V8 together with the water containing SO ₄ ^2- . The mixed gas from which H ₂ S has been decomposed and removed is exhausted through the valve V7. Specifically, the cleaning of the filler layer 15 with the high-pressure water is performed by filling the filler layer 15 with water and then supplying high-pressure water from the bottom of the filler layer 15 and cleaning with bubbles, or by using high-pressure water. Is preferably supplied from under the filler layer 15 and filled with water while the filler layer 15 is washed with bubbles.

  Moreover, in order to maintain the quality of the circulating water supplied to the absorption tower 3, it is desirable to open the valve V4 regularly. Thereby, a part of the circulating water is extracted, and the extracted water is drained. When the amount of circulating water becomes equal to or less than a predetermined amount due to this extraction, the water supply pump 5 opens the valve V5 and supplies the insufficient amount of water from the water supply tank 4. As the water used at this time, as described in the first embodiment, sand filtration water from the sand filtration facility of the treated water provided downstream of the final sedimentation basin of the sewage treatment plant is used. It is also possible to use treated water obtained by treating waste water such as tap water, well water or sewage.

Since it is the above structures, in the digestion gas deoxygenation method and apparatus which concern on this invention, there exist the following effects.
1) In addition to the operational effects of the deoxygenation method and apparatus described in 1) to 4) above, the following operational effects are further exhibited. That is, there is almost no methane gas in the high-pressure water extracted from the absorption tower, and conversely, most of the carbon dioxide and sulfur-based impurities in the digestion gas are present in the high-pressure water. Without worrying about preventing the explosion of the gas containing carbon dioxide and sulfur-based impurities generated in this manner, optimum desulfurization can be realized by appropriately adding oxygen according to the amount of H ₂ S contained in the gas.
2) Moreover, since the mixed gas containing carbon dioxide and sulfur impurities and oxygen supplied to the biological desulfurization tower hardly contains methane gas as described in 1) above, a sulfur system such as H ₂ S is used. Desulfurization in which the biological desulfurization tower as the impurity removal processing unit is made compact can also be realized.
3) Moreover, since hydrogen obtained by electrolysis of water has high purity, there is little contamination with impurities, and the purity of the purified gas can be easily maintained.
4) Moreover, since the oxygen obtained by electrolysis is also highly pure, compared to the case where air is used as an oxygen source for biological desulfurization, the biological desulfurization tower as a removal treatment section for sulfur impurities such as H ₂ S Desulfurization with a more compact can be realized.

  Moreover, in this Embodiment, although the example of the water stored in the water supply tank 4 was demonstrated as water introduce | transduced from the upper part of the biological desulfurization tower 16, it is not necessarily limited to this. For example, waste water discharged from the valve V4 may be introduced from the upper part of the biological desulfurization tower 16. Moreover, you may introduce | transduce the water (for example, 30-50 degreeC) utilized for cooling of compressor 2a, 2b from the upper part of the biodesulfurization tower 16. FIG.

In the present embodiment, the sulfur-based impurities such as carbon dioxide and H ₂ S are separated from the water in which the sulfur-based impurities such as carbon dioxide and H ₂ S extracted from the decompression tank 13 are dissolved. a sulfur-based impurities of carbon dioxide and H _{2 S} or the like is an example has been described for mixing a new oxygen supplied from water electrolysis apparatus 6 is not necessarily limited thereto. For example, vacuum vaporization tower sulfur-based impurities of carbon dioxide and H _{2 S} or the like withdrawn from the tank 13 had a sulfur-based impurities suction hole such carbon dioxide and H _{2 S} in water dissolved (gas-liquid separating means : Atmospheric pressure is released through a suction hole (not shown) to vaporize sulfur-based impurities such as carbon dioxide and H ₂ S into the vaporization tower, and the vaporized carbon-based impurities and sulfur-based impurities such as H ₂ S The new oxygen supplied from the water electrolysis apparatus 6 may be mixed in the vaporization tower. In addition, the new oxygen is not supplied before sulfur-based impurities such as carbon dioxide and H ₂ S are supplied to the biological desulfurization tower 16, but the new oxygen is supplied directly to the biological desulfurization tower 16. It does not matter if it is configured. In the present embodiment, the water electrolysis apparatus is a type that generates hydrogen and oxygen, and has been described with respect to an example in which H ₂ S is biologically decomposed (biodesulfurized) using oxygen. However, the present invention is not necessarily limited thereto, and if the water electrolysis device is a type that generates hydrogen and ozone, it is possible to decompose (desulfurize) H ₂ S using ozone (O ₃ ).

In the present embodiment, the decompression tank 13 is provided in order to increase the recovery rate of methane gas. For example, without providing the decompression tank 13, sulfur-based impurities such as carbon dioxide and H ₂ S are provided from the absorption tower 3. There withdrawn pressure water dissolved, sulfur dioxide and H _{2 S} and the like from water sulfur based impurities dissolved carbon dioxide and H _{2 S} or the like in the vaporization column (gas-liquid separation means) by atmospheric pressure relief, etc. A configuration for separating system impurities is also within the technical scope of the present invention. That is, at least the high-pressure water in which sulfur impurities such as carbon dioxide extracted from the absorption tower 3 and H ₂ S are dissolved is decompressed, and the sulfur carbon such as carbon dioxide extracted from the absorption tower 3 and H ₂ S is extracted. What is necessary is just a separation means having a function of separating sulfur-based impurities such as carbon dioxide and H ₂ S from water in which impurities are dissolved.

  Further, in the present embodiment, an example in which Thiobacillus bacteria are used as the sulfur-oxidizing bacteria attached to the filler layer 15 has been described, but the present invention is not necessarily limited thereto.

  In addition, although this Embodiment demonstrated the structure added to Embodiment 1, it is not necessarily limited to this, Of course, it can also be set as the structure added to Embodiment 2 or Embodiment 3. It is.

DESCRIPTION OF SYMBOLS 1 Mist separator 2a, 2b Gas compressor 3 Absorption tower 4 Water supply tank 5 Water supply pump 6 Water electrolysis apparatus 7 Pd catalyst 8 Catalyst tower 9 Dehumidifier 10 Water circulation pump 11, 20 Heat exchanger 12 Chiller 13 Pressure reduction tank 14 Dissipation Tower 15 Packing material layer 16 Biodesulfurization tower 17 H ₂ S concentration meter 30 Detection means 40 Flow path switching valve

Claims (12)

The digestion gas generated by subjecting the organic waste to methane fermentation is compressed and compressed by a compressor, the pressurized digestion gas is supplied to an absorption tower, and the digestion gas and water pressurized in the absorption tower are supplied. By contacting in a high pressure state, carbon dioxide and sulfur impurities contained in the pressurized digestion gas are dissolved in high pressure water to separate the carbon dioxide and sulfur impurities from the pressurized digestion gas, thereby purifying methane gas. Process,
Adding hydrogen to the purified methane gas (hereinafter referred to as “purified gas”);
Supplying the purified gas to which the hydrogen has been added to a catalyst tower packed with a catalyst, converting oxygen remaining in the purified gas to which the hydrogen has been added by catalytic reaction into water, and removing the oxygen;
Depressurizing the high-pressure water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved, and the carbon dioxide and water from the water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved. A step of separating sulfur impurities;
Supplying oxygen to the separated carbon dioxide and sulfur impurities;
The separated carbon dioxide and sulfur-based impurities and the newly supplied oxygen are supplied to a biological desulfurization tower having a filler layer to which microorganisms that decompose sulfur-based impurities are attached, and the action of the microorganisms is utilized. Decomposing sulfur impurities in a mixed gas in which the carbon dioxide and sulfur impurities and the newly supplied oxygen are mixed;
A method for deoxidizing digestive gas, comprising: The method for deoxidizing digestion gas according to claim 1 , further comprising a step of cooling the purified gas after the oxygen remaining in the purified gas is converted to water by a heat exchanger. The concentration of at least one of methane, carbon dioxide, and H ₂ S in the purified gas at the outlet of the absorption tower is detected. If the detected gas concentration is not within a specified value range, the absorption is performed. The purified gas at the outlet of the tower is bypassed to other than the catalyst tower by a flow path switching valve, and when the detected gas concentration is within a specified value range, the purified gas at the outlet of the absorption tower is bypassed by the flow path switching valve. deoxygenation method digestion gas according to claim 1 or 2, characterized in that had feeding to the catalyst tower. The method for deoxidizing digestion gas according to any one of claims 1 to 3 , wherein the hydrogen and the newly supplied oxygen are obtained by electrolyzing water. The catalyst layer space velocity SV of the purified gas in which the hydrogen supplied to the catalyst column is added, 7,000H ^-1 or less (zero is not included) of claims 1 to 4, characterized in that it is The method for deoxidizing digestion gas according to any one of the above. In the step of adding hydrogen to the purified gas, relative to the amount of oxygen remaining the amount of hydrogen in the purified gas, any one of claims 1 to 5, characterized in that it has two or more at a molar ratio of 1 The method for deoxidizing digestive gas according to Item. A compressor that compresses and pressurizes digestion gas generated by methane fermentation of organic waste;
The digestion gas and water pressurized by the compressor are received and contacted in a high-pressure state to dissolve carbon dioxide and sulfur impurities contained in the pressurized digestion gas in high-pressure water and from the pressurized digestion gas. An absorption tower for separating carbon dioxide and sulfur impurities and purifying methane gas;
Hydrogen supply means for adding hydrogen to the purified methane gas (hereinafter referred to as “purified gas”);
A catalyst tower that receives a purified gas to which hydrogen has been added by the hydrogen supply means, and is filled with a catalyst that converts and removes oxygen remaining in the purified gas to which hydrogen has been added; and
Depressurizing the high-pressure water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved, and the carbon dioxide and water from the water in which the carbon dioxide and sulfur impurities extracted from the absorption tower are dissolved. Separation means for separating sulfur impurities;
Oxygen supply means for supplying new oxygen to the separated carbon dioxide and sulfur impurities;
A biological desulfurization tower having a filler layer to which the separated carbon dioxide and sulfur-based impurities and new oxygen supplied from the oxygen supply means are received and microorganisms that decompose the sulfur-based impurities are attached;
A digestion gas deoxygenation apparatus comprising: The digestion gas deoxygenation apparatus according to claim 7 , further comprising a heat exchanger for cooling the purified gas exiting from the catalyst tower at a stage subsequent to the catalyst tower. Detecting means for detecting the concentration of at least one of methane, carbon dioxide, and H ₂ S in the purified gas at the outlet of the absorption tower between the absorption tower and the catalyst tower; and the detection means And a flow path switching valve provided between the catalyst towers, and when the concentration of the gas detected by the detection means is not within a specified value range, purified gas at the outlet of the absorption tower is supplied to the flow path switching valve. When the gas concentration detected by the detection means is within the specified range, the purified gas at the outlet of the absorption tower is supplied to the catalyst tower by the flow path switching valve. The digestion gas deoxygenation apparatus according to claim 7 or 8 , wherein the digestion gas deoxygenation apparatus is configured. The digestion gas deoxygenation apparatus according to any one of claims 7 to 9 , wherein the hydrogen supply means and the oxygen supply means are water electrolysis apparatuses. The catalyst layer space velocity SV of the purified gas in which the hydrogen supplied to the catalyst column is added, 7,000H ^-1 or less (zero is not included) of claims 7 to 10, characterized in that it is The digestion gas deoxygenation apparatus of any one of Claims 1. The digestion according to any one of claims 7 to 11 , wherein the amount of hydrogen added by the hydrogen supply means is 2 or more in molar ratio to the amount of oxygen remaining in the purified gas. Gas deoxygenator.

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