JPS58122018A - Treating method of methane fermentation gas - Google Patents

Treating method of methane fermentation gas

Info

Publication number
JPS58122018A
JPS58122018A JP57003595A JP359582A JPS58122018A JP S58122018 A JPS58122018 A JP S58122018A JP 57003595 A JP57003595 A JP 57003595A JP 359582 A JP359582 A JP 359582A JP S58122018 A JPS58122018 A JP S58122018A
Authority
JP
Japan
Prior art keywords
gases
pressure
carbon dioxide
gas
increased
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP57003595A
Other languages
Japanese (ja)
Inventor
Masaru Uno
宇野 優
Satoshi Ihara
井原 郷司
Takeo Tanabe
田辺 武男
Masakatsu Hiraoka
平岡 正勝
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Seika Chemicals Co Ltd
Original Assignee
Seitetsu Kagaku Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Seitetsu Kagaku Co Ltd filed Critical Seitetsu Kagaku Co Ltd
Priority to JP57003595A priority Critical patent/JPS58122018A/en
Priority to CA000401166A priority patent/CA1202576A/en
Priority to DE8282301989T priority patent/DE3272104D1/en
Priority to AT82301989T priority patent/ATE20831T1/en
Priority to EP19820301989 priority patent/EP0083832B1/en
Priority to AU83115/82A priority patent/AU550377B2/en
Priority to MX19282882A priority patent/MX161080A/en
Publication of JPS58122018A publication Critical patent/JPS58122018A/en
Priority to US06/581,208 priority patent/US4581044A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02CCAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
    • Y02C20/00Capture or disposal of greenhouse gases
    • Y02C20/40Capture or disposal of greenhouse gases of CO2

Abstract

PURPOSE:To recover carbon dioxide by applying a pressure swing method utilizing adsorbents. CONSTITUTION:Since the gases generated from a methane fermentation tank 1 contain usually impurities such as gaseous hydrogen sulfide, the gases are passed through a desulfurizing device 2 and are then increased in pressure to necessary pressure by a pressure increasing machine 3. Needless to say, in the case of fermentation gases contg. no hydrogen sulfide or the like, there is no need for any desulfurizing device and the pressure of said gases is increased as it is. The gases increased in pressure are cooled with a cooler 4 to reduce the moisture therein; thereafter, the gases are introduced into an adsorption tower 5 packed therein with adsorbents. The tower is constituted of at least two towers. If the number of the tower increases, the rate of recovery increases as well, but initial costs increase correspondingly; therefore, usually said tower is constituted of 2-6 units. With this pressure swing device, the carbon dioxide in the fermentation gases is adsorbed, and the concn. of methane in the gases is increased. Said gases are fed to the user side through a buffer tank 8. The adsorbed carbon dioxide is evacuated and desorbed by a vacuum pump 6.

Description

【発明の詳細な説明】 本発明はメタン発酵ガスの処理方法に関する。[Detailed description of the invention] The present invention relates to a method for treating methane fermentation gas.

さらに詳しくはメタン発酵法で発生したガス中の炭酸ガ
スをプレッシャースイング法(交互圧力変動法)により
回収する方法に関するものである。
More specifically, the present invention relates to a method for recovering carbon dioxide gas in gas generated by a methane fermentation method using a pressure swing method (alternate pressure fluctuation method).

酵ガスである下水汚泥の消化メタン発酵ガスには通常3
5〜40Vo1%の炭酸ガスが含まれている。
Digested methane fermentation gas from sewage sludge, which is fermentation gas, usually contains 3
Contains 5 to 40 Vo1% carbon dioxide gas.

このため発熱量が低く用途が制限されていた。For this reason, its use was limited due to its low calorific value.

きるものである。It is possible.

本発明者らはこの点に着目し検討を重ねた結果、炭酸ガ
スの除去にプレッシャースイング法を用いることに想到
し本発明に到った。
The present inventors focused on this point and, as a result of repeated studies, came up with the idea of using a pressure swing method to remove carbon dioxide gas, and arrived at the present invention.

従来一般に廃ガス中の炭酸ガスを1収′除去する方法と
しては、アルカリ液、例えばアミン水溶液や炭酸カリウ
ム水溶液で吸収し加熱再生する化学吸収法、加圧水によ
り吸収し減圧放散する水吸収法が知られている。 しか
し前者は再生時に大量の熱エネルギーを必要とし、後者
の場合は物理吸収のため30 kv/cjG!i!度の
^圧にする必要があり、日収コストが高くなるのでメタ
ン発酵ガスには適当でない。 またメタン発酵ガス中の
炭酸がスを除去する方法として、特開昭56−1187
91号公報に、メタン発酵ガスをタンク内で水と接触さ
せ、吸収水をタンク外へ取出して大気中へ放散させる方
法が記載されているが、この方法はar”m したプレ
ッシャースイング法により炭酸ガスを回収する方法を見
出したものである。
Conventionally known methods for removing carbon dioxide gas from waste gas in one yield include the chemical absorption method, which involves absorbing with an alkali solution such as an amine aqueous solution or potassium carbonate aqueous solution and regenerating it by heating, and the water absorption method, which absorbs it with pressurized water and releases it under reduced pressure. It is being However, the former requires a large amount of thermal energy during regeneration, and the latter requires 30 kV/cjG due to physical absorption! i! It is not suitable for methane fermentation gas because it needs to be at a pressure of 30°C and the daily production cost is high. In addition, as a method for removing carbon dioxide from methane fermentation gas, JP-A-56-1187
Publication No. 91 describes a method in which methane fermentation gas is brought into contact with water in a tank, and the absorbed water is taken out of the tank and diffused into the atmosphere. They discovered a way to recover gas.

即ら本発明の要旨は、メタン発酵法で発生したガス中の
炭酸ガスをプレッシャースイング法により回収する方法
である。 本発明の方法によれば吸着圧力も低く、必要
エネルギーも加圧に要する電力だけであり、加圧発酵槽
の場合はこれも必要なく、極めて経済的に炭酸ガスを回
収し得る。
That is, the gist of the present invention is a method for recovering carbon dioxide gas in gas generated by a methane fermentation method using a pressure swing method. According to the method of the present invention, the adsorption pressure is low and the energy required is only the electric power required for pressurization, which is not necessary in the case of a pressurized fermenter, and carbon dioxide gas can be recovered extremely economically.

本発明の方法により炭酸ガスを除去されたメタン発酵ガ
スは昇圧された圧力でプレッシャースイング装置から送
り出されるから、使用するのに有利である。 例えばガ
スエンジンやガスタービン等の熱III閏の燃料として
利用する場合は加圧状態のまま熱機関に使用できるため
過給器付エンジンにそのまま利用できる。
The methane fermentation gas from which carbon dioxide has been removed by the method of the invention is advantageous for use since it is delivered from the pressure swing device at increased pressure. For example, when it is used as a fuel for a heat III engine such as a gas engine or a gas turbine, it can be used in a heat engine in a pressurized state, so it can be used as it is in a supercharged engine.

本発明のプレッシャースイング法の圧力が10に=t/
cdGを超えると装置費が^価になり、これに斗オライ
ド系モレキュラーシープ、シリカゲル、アルミナゲル等
市販の各種吸着剤を使用できるが、カーボンモレキュラ
ーシープを使用すると、吸着剤単位容積あたりの処理能
力が多きく、かつガスの残留水分に対する抵抗性が大き
く、耐用年数が長くなるので他の吸着剤に比べて有利で
ある。
The pressure of the pressure swing method of the present invention is 10 = t/
If it exceeds cdG, the equipment cost will increase, and various commercially available adsorbents such as doo-olide molecular sheep, silica gel, alumina gel, etc. can be used for this, but if carbon molecular sheep is used, the processing capacity per unit volume of adsorbent will be lower. It is advantageous compared to other adsorbents because it has a high resistance to residual moisture in the gas and has a long service life.

メタン発酵槽で発生するガスの濃度は通常35℃程度か
もしくは55℃程度で、いずれも水分飽和の状態である
から、これを少なくとも40℃以下、好ましくは20’
CI!i!度に冷却して水分を減少させるのが望ましい
。 しかし吸着剤の種類によっては更に低温にして脱水
、乾燥する必要があるので、この点に於ても前記のよう
にカーボンモレキュラーシープを使用すると有利である
The concentration of gas generated in a methane fermentation tank is usually around 35°C or 55°C, both of which are saturated with water, so the concentration should be at least 40°C or lower, preferably 20°C.
CI! i! It is desirable to reduce moisture content by cooling to a certain degree. However, depending on the type of adsorbent, it may be necessary to dehydrate and dry it at a lower temperature, so in this respect as well, it is advantageous to use carbon molecular sheep as described above.

以下第一図に示すフローシートに従って本発明を説明す
る。
The present invention will be explained below according to the flow sheet shown in FIG.

メタン発酵槽1から発生したガスは、通常硫化水素ガス
等の不純物を含んでいるため、脱硫器2を通した後昇圧
lll3で必要な圧力に昇圧される。
The gas generated from the methane fermentation tank 1 usually contains impurities such as hydrogen sulfide gas, so after passing through the desulfurizer 2, the gas is boosted to a required pressure in a pressure booster 113.

当然のことながら硫化水素等を含まない発酵ガスの場合
には脱硫器は不要でありそのまま昇圧する。
Naturally, if the fermentation gas does not contain hydrogen sulfide or the like, a desulfurizer is not necessary and the pressure is increased as is.

1圧されたガスはクーラー4で冷却し水分を下げ’y*
、吸着剤が充填された吸着塔5に導入される。
The gas pressurized to 1 pressure is cooled by cooler 4 to lower the moisture content.
, is introduced into an adsorption tower 5 filled with an adsorbent.

吸着塔は最低2塔より構成される、塔数が多くなれば回
収率も上昇するが、設備費も上るので通常は2〜6塔で
構成される。 本プレッシャースイング装置で発酵ガス
中の炭酸ガスが吸着され、ガス中のメタン濃度が上昇し
、バッファータンク8を通じ7利用側に送られる。 一
方吸着塔5内に吸着された炭酸ガスは真空ポンプ6によ
って減圧脱糖される。
The adsorption tower is composed of at least two towers, and although the recovery rate increases as the number of towers increases, the equipment cost also increases, so it is usually composed of two to six towers. This pressure swing device adsorbs carbon dioxide gas in the fermentation gas, increases the methane concentration in the gas, and sends it to the usage side 7 through the buffer tank 8. On the other hand, the carbon dioxide gas adsorbed in the adsorption tower 5 is desugarized under reduced pressure by the vacuum pump 6.

大気圧[の場合は当然真空ポンプ6は不要である。 脱
着された炭酸ガスは貯槽7を軽て使用に供する。 この
炭酸ガスは用途によりそのまま輸送して使用するか、あ
るいは従来の液化炭酸ガス報造設備に導入され液化炭酸
ガスを親造する。
Naturally, in the case of atmospheric pressure, the vacuum pump 6 is not necessary. The desorbed carbon dioxide makes the storage tank 7 available for light use. Depending on the purpose, this carbon dioxide gas may be transported and used as is, or it may be introduced into conventional liquefied carbon dioxide production equipment to produce liquefied carbon dioxide gas.

以下具体的に本発明の実施態様を説明する。Embodiments of the present invention will be specifically described below.

下水処理工場より発生する下水汚泥の処理のため、婚気
性発酢(いわゆるメタン発酵)により発生するガスはそ
の成分が炭酸ガス30〜35Vo1%残りがメタンでそ
の外に少量の水素、窒素及び酸ガスが除去され、5v0
1%の炭酸ガスを含む^カロリーに精製される。 この
ガスを従来利用されているガスエンジンに利用すると、
炭酸ガスを除去していないメタン発酵ガスに比ベカロリ
ーが5000〜6000KaIl/N−から8000K
cal/N♂に増加し、ガスエンジンの燃料として使用
する場合、その効率が約25%増加した。 一方真空ポ
ンプを用いて70 torrまで減圧lI21された炭
酸ガスは純度99%で得られた。 これは従来の液化炭
酸ガス原料として充分な純度である。
For the treatment of sewage sludge generated from sewage treatment plants, the gas generated by aqueous acid production (so-called methane fermentation) is composed of 30 to 35 volts of carbon dioxide, the remainder being methane, and a small amount of hydrogen, nitrogen, and acid. Gas removed, 5v0
Contains 1% carbon dioxide and is refined into calories. When this gas is used in conventional gas engines,
Compared to methane fermentation gas from which carbon dioxide gas has not been removed, the calories are 5,000 to 6,000 Kal/N- to 8,000 K.
cal/N♂, and its efficiency increased by about 25% when used as fuel for gas engines. On the other hand, carbon dioxide gas whose pressure was reduced to 70 torr using a vacuum pump was obtained with a purity of 99%. This is of sufficient purity as a conventional liquefied carbon dioxide raw material.

この場合の電力は0.15KW/Nf発酵ガスであり、
従来方法に比べ非常に経済的であり、ガスエンジンの効
率向上による電力発生最の約1/3で充分であり、エネ
ルギーバランス上非常に経済的である。
The electric power in this case is 0.15KW/Nf fermentation gas,
It is very economical compared to the conventional method, and only about 1/3 of the electricity generated due to the improved efficiency of the gas engine is sufficient, making it very economical in terms of energy balance.

なお本発明の方法は下水処理汚泥のメタン発酵ガスのみ
ならず、バイオマスシステムなどの炭酸ガスを含むメタ
ンガスの処理に適用することができる。
The method of the present invention can be applied not only to methane fermentation gas from sewage treatment sludge, but also to the treatment of methane gas containing carbon dioxide gas in biomass systems and the like.

出願人   親鉄化学工業株式会社 代表者  佐々木 浩 手続補正型 昭和57年2月Zす 1、 特許出願の表示  昭和57年特許願第06My
r号2、 発明の名称    メタン発酵ガスの処理方
法a、 補正をする者 事件との関係    特許出願人 郵便番@    673−01 住 所    兵庫県txtfiiii5MWa 4 
e番地の1名 称    −鉄化学工業株式会社 4、補正命令の日付      自   発1  5、
補正の対象        願書および明細書6、補正
の内容 昭和57年1月12日差出の願書および明S書を別紙の
とおり提出します(浄書につき内容に変更なし)以  
Applicant: Shintetsu Kagaku Kogyo Co., Ltd. Representative: Hiroshi Sasaki Procedural Amended Type February 1980 Zsu1, Indication of Patent Application: 1981 Patent Application No. 06 My
r No. 2, Title of the invention Method for treating methane fermentation gas a, Relationship to the case of the person making the amendment Patent applicant postal code @ 673-01 Address Hyogo prefecture txtfiii5MWa 4
First name of address e - Tetsu Kagaku Kogyo Co., Ltd. 4, Date of amendment order Voluntary 1 5,
Subject of amendment Application and Specification 6, contents of amendment The application and Memorandum S sent on January 12, 1980 are submitted as attached (there are no changes in the contents as they are engravings).
Up

Claims (1)

【特許請求の範囲】 (1)メタン発酵法で発生したガス中の炭酸ガスをプレ
ッシャースイング法により回収する方法。 ;、(2>プレッシャースイング法の畷着圧力が大;負
圧以上10Ka /jG以下である特許請求の範囲(1
)記載の方法。 (1)記載の方法。 シープを用いる特許請求の範囲(1)記載の方法。 (6)発生ガスの温度を40℃以下にして処理する特許
請求の範囲(1)に記載の方法。 (7)脱硫機構を備えたプレッシャースイング法を用い
る特許請求の範fl(1)記載の方法。
[Claims] (1) A method for recovering carbon dioxide gas in gas generated by a methane fermentation method using a pressure swing method. ;, (2> Claims in which the furrowing pressure of the pressure swing method is large; negative pressure or more and 10 Ka/jG or less (1)
) method described. (1) The method described. The method according to claim (1) using sheep. (6) The method according to claim (1), wherein the temperature of the generated gas is reduced to 40° C. or lower. (7) The method according to claim fl(1), which uses a pressure swing method equipped with a desulfurization mechanism.
JP57003595A 1982-01-12 1982-01-12 Treating method of methane fermentation gas Pending JPS58122018A (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
JP57003595A JPS58122018A (en) 1982-01-12 1982-01-12 Treating method of methane fermentation gas
CA000401166A CA1202576A (en) 1982-01-12 1982-04-16 Process for separating carbonic acid gas from methane- rich gas
DE8282301989T DE3272104D1 (en) 1982-01-12 1982-04-19 Process for separating carbonic acid gas from methane-rich gas
AT82301989T ATE20831T1 (en) 1982-01-12 1982-04-19 PROCESS FOR SEPARATION OF DE CO2 FROM A METHANE-RICH GAS.
EP19820301989 EP0083832B1 (en) 1982-01-12 1982-04-19 Process for separating carbonic acid gas from methane-rich gas
AU83115/82A AU550377B2 (en) 1982-01-12 1982-04-29 Separation of carbonic acid gas from methane rich gas
MX19282882A MX161080A (en) 1982-01-12 1982-05-24 PROCEDURE FOR SEPARATING GAS FROM CARBONIC ACID FROM GAS RICH IN METHANE
US06/581,208 US4581044A (en) 1982-01-12 1984-02-21 Process for separating carbonic acid gas from methane-rich gas

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57003595A JPS58122018A (en) 1982-01-12 1982-01-12 Treating method of methane fermentation gas

Publications (1)

Publication Number Publication Date
JPS58122018A true JPS58122018A (en) 1983-07-20

Family

ID=11561821

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57003595A Pending JPS58122018A (en) 1982-01-12 1982-01-12 Treating method of methane fermentation gas

Country Status (1)

Country Link
JP (1) JPS58122018A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100810721B1 (en) 2007-08-29 2008-03-07 (주)대성그린테크 Ds-lrs

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5360394A (en) * 1976-10-15 1978-05-30 Air Prod & Chem Method of purifying hydrogen by selective adsorption

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5360394A (en) * 1976-10-15 1978-05-30 Air Prod & Chem Method of purifying hydrogen by selective adsorption

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100810721B1 (en) 2007-08-29 2008-03-07 (주)대성그린테크 Ds-lrs

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