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JPS6041522A - Method and apparatus for purifying gaseous mixture - Google Patents

Method and apparatus for purifying gaseous mixture

Info

Publication number
JPS6041522A
JPS6041522A JP59109789A JP10978984A JPS6041522A JP S6041522 A JPS6041522 A JP S6041522A JP 59109789 A JP59109789 A JP 59109789A JP 10978984 A JP10978984 A JP 10978984A JP S6041522 A JPS6041522 A JP S6041522A
Authority
JP
Japan
Prior art keywords
gas
reactor
purifying
adsorption
gas stream
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
JP59109789A
Other languages
Japanese (ja)
Inventor
ブルクハルト・ハルダー
ベルンハルト・シユトリツカー
カール・クノープラウフ
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.)
Bergwerksverband GmbH
Original Assignee
Bergwerksverband GmbH
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 Bergwerksverband GmbH filed Critical Bergwerksverband GmbH
Publication of JPS6041522A publication Critical patent/JPS6041522A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/0462Temperature swing adsorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2256/00Main component in the product gas stream after treatment
    • B01D2256/10Nitrogen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/402Further details for adsorption processes and devices using two beds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/0407Constructional details of adsorbing systems
    • B01D53/0438Cooling or heating systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Separation Of Gases By Adsorption (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、吸着反応器円の吸着剤層をガ2成分の一部分
を吸着させながら生ガスを貫流させかつ1種以上のガス
成分を吸着剤層の端部から流出させかつ生ガス流を生産
ガスと残余ガス流とに分解する常用の圧力変化吸着技術
によってガス混合物である生ガ2を精製する方法及び装
置に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is directed to an adsorption reactor in which raw gas flows through the adsorbent layer while adsorbing a portion of the two gas components, and one or more gas components are transferred to the adsorbent layer. The present invention relates to a method and apparatus for purifying a gas mixture, raw gas 2, by conventional pressure change adsorption techniques, exiting from the end of the raw gas stream and splitting the raw gas stream into a product gas and a residual gas stream.

従来技術 ガス混合物を精製又は分離しかつその際KUli着剤に
対する循環式の圧力変化吸着技術を利用することに公知
である。この方法は経済的には約−20〜+40℃の温
度範囲で実施することができる、そnというのもこの温
度範囲内でに吸着能力と選択性の間に最良の関係が存在
するからである。
It is known from the prior art to purify or separate gas mixtures and to use cyclic pressure change adsorption techniques on KUli adhesives. The process can be carried out economically in the temperature range of about -20 to +40°C, since it is within this temperature range that the best relationship between adsorption capacity and selectivity exists. be.

平均的作業温度が前記温度範囲からずfるか又は該温度
が限界領域にある場合Kに、大量の吸着剤層が必要とな
る。
If the average working temperature is outside the above-mentioned temperature range or is in the limit range, a large amount of adsorbent layer is required.

従って、最適な温度で作業しない全ての装置のエネルギ
ー需要に膨大である、このことに例えば既に日中と夜間
との一部分高い温度差においても生じ、ましてや例えば
熱帯地方における約60℃及び北極地方における約−8
0℃のような極端な気候帯におけるガス精製の場合Kに
顕著である。
Therefore, the energy demands of all equipment that do not work at optimal temperatures are enormous, and this also occurs, for example, even in already partly high temperature differences between day and night, and even more so, for example, at about 60 °C in the tropics and in the Arctic. Approximately -8
This is especially true for gas purification in extreme climate zones such as 0°C.

極端な気候状況で作動する圧力変化装置を熱絶縁するこ
とに公知である。しかしながら、そf′Lによ扛ば部分
的効果が達成さnるにすぎない、そnというのも吸着さ
nるべきガスに一般に、最適な温度範囲の著しく外にあ
る環境温度で存在するからである。本発明に上記一般的
形式において、第一に絶縁手段を利用する代シに、吸着
反応器を付加的な熱交換媒体を用いて冷却又は加熱する
技術的手段に関する、そnというのもこのために必要な
エネルギーにそn以外において必要な圧縮エネルギーよ
ムもはるかに少なくて済むからである。この方法はもち
ろんのこと熱絶縁との組合せにより、かつ全く特殊には
、熱交換器で包囲さnた吸着反応器が熱絶縁さnており
かつ断熱シールによって包囲さn並びに中間室が残余ガ
2及び/又に生産ガス流によって洗わnることにより改
善さ詐る。そnというのも、後者の手段によnば、予熱
/予冷のために生ガ、2VC導入さfた熱又は冷却エネ
ルギーを一部分なお後で利用することができるからであ
る。
It is known to thermally insulate pressure change devices operating in extreme climatic conditions. However, only a partial effect is achieved when applied to f'L, since the gas to be adsorbed is generally present at ambient temperatures that are significantly outside the optimal temperature range. It is from. It is for this reason that the invention, in the general form described above, firstly relates to technical means of cooling or heating the adsorption reactor with the aid of an additional heat exchange medium, instead of using insulation means. This is because the compression energy required for other than the energy required for is also much smaller. This method, of course, in combination with thermal insulation, and quite specifically, involves an adsorption reactor surrounded by a heat exchanger, thermally insulated and surrounded by a thermally insulating seal, and an intermediate chamber surrounded by a residual gas. 2 and/or improved by washing with a production gas stream. This is because, by means of the latter measure, a portion of the heat or cooling energy introduced for preheating/precooling can still be used later.

発明が解決しようとする問題点 本発明の課題に、前記欠点を排除しかつ吸着剤量並びに
分離すべき生ガス混合物のための圧縮エネルギーをでき
るだけ少なくした冒頭に記載の形式の方法及び装置を提
供することであった。
SUMMARY OF THE INVENTION It is an object of the invention to provide a method and a device of the type mentioned at the outset, which eliminates the above-mentioned disadvantages and in which the amount of adsorbent and the compression energy for the raw gas mixture to be separated are as low as possible. It was to do.

問題点を解決するだめの手段 前記課題は、前記形式の方嫉において本発明の第1番目
の発明によnば、吸着反応器の温度を熱交換媒体を用い
て一20〜+40℃の温度に保持することによシ解決さ
扛、第2番目の発明によnば、吸着反応器の温度を熱交
換媒体を用いて一20〜+40℃の温度範囲に保持しか
つガス流の一部を吸着反応器と該反応器を包囲スル断熱
シールドとの間に形成さ扛た中空室を貫流させることに
よシ解決される。
Means for Solving the Problems According to the first aspect of the present invention, the above-mentioned problem is solved by adjusting the temperature of the adsorption reactor to a temperature of -20 to +40°C using a heat exchange medium. According to the second invention, the temperature of the adsorption reactor is maintained in the temperature range from -20 to +40 °C by means of a heat exchange medium and a part of the gas stream is The solution is to allow the flow to flow through a hollow chamber formed between an adsorption reactor and an insulating shield surrounding the reactor.

更に装置に関しては、前記形式の装置において、反応器
が熱絶縁層内に埋設さnた冷却蛇管を有し、該蛇管が導
管と接続さtかつ反応器を包囲する中空室と共に断熱シ
ールド内に配置さnていることにより解決さnる。該装
置の有利な実施態様は特許請求の範囲第4項に記載さn
ている。
Further regarding the apparatus, in an apparatus of the type described, the reactor has a cooling coil embedded in a thermally insulating layer, which coil is connected to a conduit and is located in an insulating shield together with a hollow chamber surrounding the reactor. This is solved by placing the An advantageous embodiment of the device is set out in claim 4.
ing.

実施例 空気から窒素を生産する際KFI、例えば作業温度20
℃及び所望の窒素純度999%の場合17パール及び生
産ガ−2300m/hで吸着剤層10.5m”75♂必
要である。空気需要[1200ゴ/hである。平均作業
温度40℃でその他は同じ圧力条件で同じ窒素生産速度
を達成すべきS @ vc B、はとんど2倍の大量(
16,8m3)の吸着が必要でありかつ空気需要にその
際約1845 m’ / hである。床温度20℃でP
SA装置のための全エネルギ=需要1d 194 KW
 であるが、そ扛に対して床温度牛○℃でに310 K
W になる1、吸着容器及び流入空気を20℃に冷:i
g+するためには、エネルギー消費量ば24KWlcf
iる。従って、ガス精製を40℃でなく、20℃で実施
すn、ば、約100 KWのエネルギー利得が達成づf
ることになる。
Examples When producing nitrogen from air, KFI, e.g. working temperature 20
For a desired nitrogen purity of 999% and 17 pearls and a production gas of 2300 m/h, an adsorbent layer of 10.5 m"75♂ is required. Air demand [1200 g/h. should achieve the same nitrogen production rate under the same pressure conditions S @ vc B, is almost twice as large (
16.8 m3) is required and the air demand is approximately 1845 m'/h. P at bed temperature 20℃
Total energy for SA equipment = demand 1d 194 KW
However, the floor temperature for the air is 310 K at ○℃.
1. Cool the adsorption vessel and incoming air to 20°C: i
To achieve g+, energy consumption is 24KWlcf.
iru. Therefore, if gas purification is carried out at 20°C instead of 40°C, an energy gain of about 100 KW can be achieved.
That will happen.

以下に、本発明の別の利点及び実施態様を図面に示した
不利な1実施例につき釘細に説明する。
In the following, further advantages and embodiments of the invention will be explained in more detail with reference to a disadvantageous embodiment shown in the drawing.

図面には、常用の圧力変化吸着技術を用いたガ;2混合
物c生ガヌ)の精製装置が略示さnている。この装ji
7iげ圧力変化装置から成り、そのうちの2つの反応器
1及び接続導管2〜4のみが示さ扛ている。反応器に熱
絶縁層10内に埋設さnた蛇管5によって包囲さn、該
蛇管は冷却/加熱装置6と接続さnている。熱帯地方で
に冷却装置が、北極地方では加熱装置が必要である。蛇
管並びに熱絶縁層に熱工学に基づき構成さnている。
The drawing schematically shows an apparatus for the purification of a mixture of raw moths and moths using conventional pressure change adsorption techniques. This outfit
It consists of a 7-meter pressure change device, of which only two reactors 1 and connecting conduits 2 to 4 are shown. The reactor is surrounded by a corrugated tube 5 embedded in a thermally insulating layer 10, which is connected to a cooling/heating device 6. Cooling equipment is required in the tropics and heating equipment is required in the Arctic. The flexible tube and thermal insulation layer are constructed based on thermal engineering.

導管2を経て、コンプレツヤ7により作業圧に補償さn
た空気にまず熱交換器8内で15℃に冷却されかつ循環
式で両者の反応器の一方に導入さnる。生産さnた窒素
は導管3を介して圧力変化装置から流出し、一方約20
℃i有する残余ガスに導管牛を介して断熱/−ルrgと
反応器1の熱絶縁層10との間に形成さnた中空室11
に流入する。
Via the conduit 2, the compressor 7 compensates the working pressure.
The air is first cooled to 15° C. in a heat exchanger 8 and introduced in a circulating manner into one of the two reactors. The produced nitrogen leaves the pressure change device via conduit 3, while about 20
A hollow chamber 11 formed between the thermally insulating layer 10 of the reactor 1 and the thermally insulating layer 10 of the reactor 1 is passed through the conduit to the residual gas having
flows into.

【図面の簡単な説明】[Brief explanation of the drawing]

図面は本発明の精製装置の1実施例の略示系統図である
。 J・・・反応器、2〜牛・・・導管、b・・冷却蛇管、
6・・・冷:IJ /加熱装置、7・・・コンプレツヤ
、81.。 熱交換器、9・・・断熱シールド、1o・・・熱絶縁層
、11・・・中空室 第1頁の続き @発明者 ベルンハルト・シュド ト リツカ− 0発 明 者 カール・クツ−プラウ ドイツ連邦共和
国ボットロープ・ニーベルンゲンヴエーク2
The drawing is a schematic system diagram of one embodiment of the purification apparatus of the present invention. J...Reactor, 2~Cow...Conduit, b...Cooling serpentine pipe,
6...Cold: IJ/heating device, 7...Compress gloss, 81. . Heat exchanger, 9... Heat insulating shield, 1o... Thermal insulation layer, 11... Hollow chamber Continued from page 1 @ Inventor Bernhard Schudt Tritzker 0 Inventor Karl Kutz-Plau Federal Republic of Germany Bottorp Nibelungenveke 2

Claims (1)

【特許請求の範囲】 l Vi着反応器内の吸着剤層をガス成分の一部分を吸
着させなから生ガスを貫流させかつ1種以上のガス成分
を吸着剤層の端部から流出させかつ生ガス流を生産ガス
と残余ガヌ流とに分解する常用の圧力変化吸着技術によ
ってガタ混合物である生ガスを精製する方法において、
吸着反応器の温度を熱交換媒体を用いて一20〜十牛O
℃の温度範囲に保持することを特徴とする、ガタ混合物
を精製する方法2 吸着反応器内の吸着剤層全ガス成分
の一部分を吸着させながら生ガスを貫流させかつ1種以
上のガス成分を吸着剤層の端部から流出させかつ生ガス
流を生産ガヌと残余ガス流とに分解する常用の圧力変化
吸着技術によってガタ混合物である生ガスを精製する方
法において、吸着反応器の温度を熱交換媒体を用いて一
20〜+40℃の温度範囲に保持しかつガヌ流の一部を
吸着反応器と該反応器を包囲−J’−ル断熱シールドと
の間に形成さ扛た中空室を貫流させることを特徴とする
、ガス混合物を精製する方法。 3 吸着反応器内の吸着剤層をガス成分の一部分を吸着
させながら化ガフを貫流させかつ1種以上のガス成分を
吸着剤層の端部から流出させかつ生ガス流を生産ガヌと
残余ガス流とに分解する常用の圧力変化吸着技術によっ
てガス混合物である生ガスを精製する装置において、反
応器(1)が熱絶縁層(10)同に埋設さ扛た冷却蛇管
(5)を有し、該蛇管が導管(2,3,4−)と接続さ
扛かつ反応器(1)を包囲する中空室(11)と共に断
熱シールl” (9)内に配置さ扛ていることを特徴と
する、ガタ混合物を精製する装置。 4、[T熱シールド(9]の外部にコンプレッサ〔7〕
、熱交換器〔8〕及び冷却/加熱装置(6)が配置さし
ている、特許請求の範囲第3項記載の装置。
[Scope of Claims] l An adsorbent layer in a Vi deposition reactor is configured to allow raw gas to flow through it without adsorbing a portion of the gas components, and to allow one or more gas components to flow out from the end of the adsorbent layer and to In a method for purifying raw gas, a gas mixture, by conventional pressure change adsorption techniques in which the gas stream is split into a product gas and a residual gas stream,
Adjust the temperature of the adsorption reactor to 120 to 10 O by using a heat exchange medium.
Method 2 for purifying a gaseous mixture, characterized in that it is maintained in a temperature range of In the process of purifying the raw gas mixture by conventional pressure change adsorption techniques, which exit from the end of the adsorbent bed and decompose the raw gas stream into a product gas stream and a residual gas stream, the temperature of the adsorption reactor is A hollow space formed between the adsorption reactor and the heat-insulating shield surrounding the reactor is maintained at a temperature range of -20 to +40°C using a heat exchange medium and a part of the Ganu flow is absorbed. A method for purifying a gas mixture, characterized in that it flows through a chamber. 3. The adsorbent layer in the adsorption reactor is made to flow through the gas gaff while adsorbing a portion of the gas component, and one or more gas components flow out from the end of the adsorbent layer, and a raw gas stream is produced and the remainder is In an apparatus for purifying a gas mixture, raw gas, by conventional pressure change adsorption techniques, the reactor (1) has a thermally insulating layer (10) and a cooling coil (5) embedded in the thermal insulation layer (10). characterized in that the serpentine tube is connected to the conduits (2, 3, 4-) and arranged in a heat insulating seal (9) together with the hollow chamber (11) surrounding the reactor (1). 4. A compressor [7] outside the T heat shield (9).
4. The device according to claim 3, wherein a heat exchanger [8] and a cooling/heating device (6) are arranged.
JP59109789A 1983-05-31 1984-05-31 Method and apparatus for purifying gaseous mixture Pending JPS6041522A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19833319664 DE3319664A1 (en) 1983-05-31 1983-05-31 Process and apparatus for purifying gas mixtures
DE3319664.8 1983-05-31

Publications (1)

Publication Number Publication Date
JPS6041522A true JPS6041522A (en) 1985-03-05

Family

ID=6200294

Family Applications (2)

Application Number Title Priority Date Filing Date
JP59109789A Pending JPS6041522A (en) 1983-05-31 1984-05-31 Method and apparatus for purifying gaseous mixture
JP1991077936U Pending JPH0499215U (en) 1983-05-31 1991-09-26

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP1991077936U Pending JPH0499215U (en) 1983-05-31 1991-09-26

Country Status (4)

Country Link
JP (2) JPS6041522A (en)
AU (1) AU2872084A (en)
DE (1) DE3319664A1 (en)
ZA (1) ZA844064B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4696681A (en) * 1986-10-01 1987-09-29 The Boc Group, Inc. PSA assembly
US5169413A (en) * 1991-10-07 1992-12-08 Praxair Technology Inc. Low temperature pressure swing adsorption with refrigeration
IT1264106B1 (en) * 1993-03-30 1996-09-10 So Di Bo S P A PURIFIER FOR ACTIVATED CARBON SOLVENTS FOR DRY CLEANING MACHINES WITH INCREASED ABSORPTION.
US5453112A (en) * 1994-02-02 1995-09-26 Praxair Technology, Inc. Pressure swing adsorption heat recovery
FR2834973B1 (en) * 2002-01-18 2005-04-15 Thermagen INSULATION OF A SELF-REFRIGERATING BEVERAGE PACKAGING
TW201043327A (en) * 2009-03-30 2010-12-16 Taiyo Nippon Sanso Corp Pressure swing adsorbing type gas separating method and separation device

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5235173A (en) * 1975-09-13 1977-03-17 Kobe Steel Ltd Cooling method of adsorbent
JPS5745321A (en) * 1980-09-03 1982-03-15 Toshiba Corp Activated carbon adsorb

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2950731C2 (en) * 1979-12-17 1985-09-19 Michael 8000 München Zoche Device for cleaning a gas

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5235173A (en) * 1975-09-13 1977-03-17 Kobe Steel Ltd Cooling method of adsorbent
JPS5745321A (en) * 1980-09-03 1982-03-15 Toshiba Corp Activated carbon adsorb

Also Published As

Publication number Publication date
AU2872084A (en) 1984-12-06
JPH0499215U (en) 1992-08-27
ZA844064B (en) 1985-01-30
DE3319664A1 (en) 1984-12-06

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