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JPS6157550B2 - - Google Patents
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JPS6157550B2 - - Google Patents

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Publication number
JPS6157550B2
JPS6157550B2 JP58132466A JP13246683A JPS6157550B2 JP S6157550 B2 JPS6157550 B2 JP S6157550B2 JP 58132466 A JP58132466 A JP 58132466A JP 13246683 A JP13246683 A JP 13246683A JP S6157550 B2 JPS6157550 B2 JP S6157550B2
Authority
JP
Japan
Prior art keywords
air
heat exchanger
expansion turbine
nitrogen
column
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.)
Expired
Application number
JP58132466A
Other languages
Japanese (ja)
Other versions
JPS6023771A (en
Inventor
Tetsuo Senchi
Takashi Ooyama
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.)
Kobe Steel Ltd
Original Assignee
Kobe Steel 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 Kobe Steel Ltd filed Critical Kobe Steel Ltd
Priority to JP13246683A priority Critical patent/JPS6023771A/en
Priority to BR8403601A priority patent/BR8403601A/en
Priority to IN525/MAS/84A priority patent/IN161955B/en
Publication of JPS6023771A publication Critical patent/JPS6023771A/en
Publication of JPS6157550B2 publication Critical patent/JPS6157550B2/ja
Granted legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
    • F25J3/04Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream for air
    • F25J3/04248Generation of cold for compensating heat leaks or liquid production, e.g. by Joule-Thompson expansion
    • F25J3/04284Generation of cold for compensating heat leaks or liquid production, e.g. by Joule-Thompson expansion using internal refrigeration by open-loop gas work expansion, e.g. of intermediate or oxygen enriched (waste-)streams
    • F25J3/0429Generation of cold for compensating heat leaks or liquid production, e.g. by Joule-Thompson expansion using internal refrigeration by open-loop gas work expansion, e.g. of intermediate or oxygen enriched (waste-)streams of feed air, e.g. used as waste or product air or expanded into an auxiliary column
    • F25J3/04303Lachmann expansion, i.e. expanded into oxygen producing or low pressure column
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
    • F25J3/04Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream for air
    • F25J3/04406Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream for air using a dual pressure main column system
    • F25J3/04412Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream for air using a dual pressure main column system in a classical double column flowsheet, i.e. with thermal coupling by a main reboiler-condenser in the bottom of low pressure respectively top of high pressure column

Landscapes

  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Mechanical Engineering (AREA)
  • Thermal Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • Separation By Low-Temperature Treatments (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は空気を液化して分離する方法に関し、
特に全低圧方式によつて空気を分離し高純度の製
品酸素を経済的に製造する方法に関するものであ
る。 空気を液化して精留することによりN2,O2
Ar等を分離する空気の液化分離装置は種々の分
野で稼動している。この種の空気液化分離装置で
は、原料空気等に対して運転条件に応じた加圧、
減圧操作を施す必要がある為、圧縮機や膨張ター
ビン等の機器の設置が不可欠である。そして空気
液化分離装置は一般に大容量のものが多く運転動
力費が嵩むため、製品酸素の製造コストの低減を
図るには精留効率を向上させると共に、運転動力
費をできる限り節約しなければならないとする産
業上の要請が強く、本発明者等もこの要請に対応
すべく特に膨張タービンについて鋭意検討を行な
つてきた。 従来の全低圧式空気分離による高純度酸素製造
方法(以下単に酸素製造方法という)は、主とし
て第1図に示す様な系統図に従つて行なわれてい
る。 以下の説明中、切換式熱交換器は特許請求の範
囲に記載の「主熱交換器」の一例であつて、例え
ば切替式吸着器を入口側に有する熱交換器等にも
適用可能である。第1図において原料空気は空気
過器1を通して供給され、空気圧縮機2で約5
Kg/cm2Gに圧縮加圧された後、アフタクーラ3で
冷却され、次に導管5により切換式熱交換器6に
導入され、精留塔8で分離精製された戻りガスに
より冷却されると共に、空気中に含まれる水分及
び炭酸ガス等が除去される。この空気は、導管7
を経て精留塔下塔(以下単に下塔という)8bに
導かれる。こうして下塔8bに導入された空気は
上昇ガスとなる一方、該下塔8bの頂部で凝縮し
て得られる還流液(富窒素液)に接触させて粗精
留し、下塔8bの頂部で富液体窒素ガスを得ると
共に、前記還流液は下塔8bの底部で酸素成分約
30〜40%の富酸素液体空気となる。下塔8bで前
述の知く粗精留された液体空気は、管路9を通つ
て液体空気過冷却器10内に導入・冷却された
後、管路11から精留塔上塔(以下単に上塔とい
う)8aの中部へ導かれる。又下塔8bの頂部に
貯留された富窒素液は管路12を通つて液体空気
過冷却器10内に導入・冷却された後、管路13
から上塔8aの上部へ導かれる。一方下塔8b内
を上昇する気体空気の一部は導管14から抜出さ
れた後、切換式熱交換器6の再熱回路15に導入
され、切換式熱交換器6の中間温度を調整した
後、調整弁16を経て、膨張タービン17に送ら
れる。膨張タービン17において約0.32Kg/cm2
に膨張され大気吸込型負荷ブロワーで外部仕事を
とり出すことによつて所要寒冷を得た空気は、導
管18を経て下塔8aに吹込まれる。但し、この
空気は富窒素ガスとして、下塔8bから抜き出さ
れた場合は上塔8aに吹きこまれることなく、不
純窒素ライン21に導入される。 こうして上塔8aで分離精製された酸素、窒
素、不純窒素は、それぞれ導管19,20,21
より抽気されて切換式熱交換器6に送られ、前述
の如く原料空気と熱交換することによつて、常温
まで温度回復を受けた後製品として取り出され、
特に酸素は導管22から図に現われらない圧縮機
により加圧された後、製品酸素として回収され
る。 又第2図に示す系統図は他の従来方法を示すも
のであつて、この従来方法の特徴は、膨張タービ
ン17の駆動時に生じる外部機械的エネルギーの
回収に当つて負荷ブロワ17aの代わりに発電機
17bを直結し、電力回収を図つている点にあ
る。 しかし上記の各従来プロセスにおける膨張ター
ビン17についての、製品酸素を得るための動力
消費原単位(以下O2原単位という)の低減は次
の点で限界があつた。それは動力の節約の仕方が
タービン容量そのものを絞り得るという直接的な
方法ではなく、エネルギー変換回収という非常に
効率の悪い間接的方法に依つているからであり、
又酸素収率増加によるO2原単位の低減について
は全く考慮されていないからである。 そこで本発明者等はO2原単位の効率的な低減
の可能性について種々検討を行なつた。 即ち、空気分離装置系の熱平衡を保つために必
要な寒冷をQ(kcal/h)とし、膨張タービン1
7の流量、断熱落差、及び効率をそれぞれE(N
m3/h)、△iad(kcal/Nm3)、η(%)とする
と、これらの変数は次式を満足しなければならな
い。 Q=E・△iad・η/100 ……(1) (1)式に於いて、Qは装置の生産量が決められれ
ば、ほぼ一意的に決まつてしまうものである。一
方、O2原単位には膨張タービン17の流量Eが
直接的に影響し、Eを低減させることがO2原単
位の低減につながる。それは以下に述べる理由で
説明される。又第5図に示す様にいま第4図に上
塔の気液平衡線、精留操作線を示す。下塔に供給
される原料空気量をA、膨張タービンへ抜き出さ
れるガス量をEとすれば、(A−E)が下塔を上
昇するガスV1となり主蒸化器で、液体酸素を蒸
発させ、上塔下部の上昇ガスV2を製造するため
に利用される。上塔下部では第4図に示されるよ
うに、操作線aと平衡線に規定されて精留が行な
われるため、操作線aは平衡線と離れている方が
精留条件は良くO2原単位は良くなる。操作線a
の傾きは、上塔下部下降液量L2と上昇ガス量V2
との比L2/V2であり、従つてO2原単位をよくす
るにはL2/V2がより小さくなるようにすればよ
い。これはとりもなおさず膨張タービン17の流
量Eをより少なくすることである。本発明ではそ
の手段として、膨張タービン17の入口圧力を、
高めることによつて△iadを増加させ、これによ
つて装置に必要な寒冷Qを確保しつつ、膨張ター
ビンの流量Eを効果的に減少させることに成功し
て完成したものであつてその構成は、主熱交換器
の再熱回路の通過せしめた下塔からの気体空気又
は気体窒素を循環熱交換器に通して昇温した後、
膨張タービンの負荷ブロワにかけて昇圧し、更に
該昇圧空気を前記循環熱交換器に通して冷却した
後、前記膨張タービンに導入する様にした点に要
旨を有するものである。 以下実施例図面に基づき本発明の構成及び作用
効果を説明するが、下記実施例は単に一代表例に
過ぎないものであつて、前・後記の趣旨に沿つて
適宜変更して実施し得ることは言うまでもない。 第3図は本発明の全低圧式空気分離方法の系統
図を示し、第1図及び第2図に夫々示す従来例と
基本的構成は同一であり、同一構成のものには同
一の符号を付し、その説明は省略する。以下本実
施例の特徴とする構成を中心に説明する。 下塔8b内の上昇空気又は窒素の一部は導管1
4から抜出された後、切換式熱交換器6の再熱回
路15に導入され、切換式熱交換器6の中間温度
を調整した後循環熱交換器25に通して常温まで
昇温せしめた後、膨張タービン17の負荷ブロワ
17aにかけて該タービン駆動による外部機械的
エネルギーを回収することにより自らはより圧縮
され昇圧する。次いで該昇圧空気をアフタクーラ
24及び循環熱交換器25に通して冷却した後、
膨張タービン17に導入する。従つて膨張タービ
ン17の入口側空気圧力は従来方法の場合に比べ
て上記機械的エネルギーの回収分だけ増加してい
るので、断熱膨張によつて生じる熱落差△iadも
それ相応に増加する。その結果、タービン流量E
については(1)式を満足し得る範囲内で減少させる
ことができるので、前述した様に上塔8a内の精
留効果が高まり、製品酸素収率は増大する。又膨
張タービン17については小型化も可能である。
従つてこれらの相乗的効果によりO2原単位を著
しく削減することができる。又図示の如く下塔8
b内からの上昇空気は負荷ブロワ17aに導入さ
れる前に循環熱交換器25により適当に昇温され
ているので、負荷ブロワ17aの運転に特に支障
を与えることもなく、又負荷ブロワ17a通過後
の昇圧空気又は窒素はアフタクーラ24内で水冷
が可能となり、循環熱交換器25による降温作用
と相まつて膨張タービン17に供給される空気の
温度特性が適正に維持される。しかし操業条件に
よつてはアフタクーラ24の設置は必ずしもも要
求されるものではない。 (実施例) 製造規模10000Nm3の酸素製造装置について第
1,2図に示す従来方法(,)及び第3図に
示す本発明方法を夫々適用した場合の1例を下記
に示す。
The present invention relates to a method for liquefying and separating air,
In particular, the present invention relates to a method for economically producing high-purity product oxygen by separating air using a completely low-pressure system. By liquefying air and rectifying it, N 2 , O 2 ,
Air liquefaction separation equipment that separates Ar, etc. is in operation in various fields. This type of air liquefaction separation equipment pressurizes the raw air etc. according to the operating conditions.
Since it is necessary to perform pressure reduction operations, it is essential to install equipment such as compressors and expansion turbines. Air liquefaction separation equipment generally has a large capacity and increases operating power costs, so in order to reduce the production cost of product oxygen, it is necessary to improve rectification efficiency and save operating power costs as much as possible. There is a strong industrial demand for this, and the inventors of the present invention have also conducted intensive studies, particularly regarding expansion turbines, in order to meet this demand. A conventional high-purity oxygen production method (hereinafter simply referred to as an oxygen production method) using total low-pressure air separation is mainly carried out according to a system diagram as shown in FIG. In the following explanation, the switching type heat exchanger is an example of the "main heat exchanger" described in the claims, and is also applicable to, for example, a heat exchanger having a switching type adsorber on the inlet side. . In FIG. 1, raw air is supplied through an air filter 1, and an air compressor 2
After being compressed and pressurized to Kg/cm 2 G, it is cooled in an aftercooler 3, then introduced into a switching heat exchanger 6 through a conduit 5, and cooled by the return gas separated and purified in a rectification column 8. , moisture, carbon dioxide, etc. contained in the air are removed. This air flows through conduit 7
It is guided to the lower column of the rectification column (hereinafter simply referred to as the lower column) 8b. The air thus introduced into the lower column 8b becomes a rising gas, while it is brought into contact with the reflux liquid (nitrogen-rich liquid) obtained by condensation at the top of the lower column 8b, and undergoes crude rectification. In addition to obtaining liquid nitrogen-rich gas, the reflux liquid has an oxygen component of about
The result is 30-40% oxygen-enriched liquid air. The liquid air crudely rectified as described above in the lower column 8b is introduced into the liquid air subcooler 10 through a pipe 9 and cooled, and then passed from the pipe 11 to the upper column of the rectification tower (hereinafter simply referred to as You will be led to the middle part of 8a (called the upper tower). Further, the nitrogen-rich liquid stored at the top of the lower column 8b is introduced into the liquid air supercooler 10 through the pipe 12 and cooled, and then passed through the pipe 13.
from there to the upper part of the upper tower 8a. On the other hand, a part of the gaseous air rising in the lower column 8b is extracted from the conduit 14 and then introduced into the reheat circuit 15 of the switching heat exchanger 6, to adjust the intermediate temperature of the switching heat exchanger 6. Thereafter, it is sent to an expansion turbine 17 via a regulating valve 16. Approximately 0.32Kg/cm 2 G in expansion turbine 17
The air, which has been expanded and obtained the necessary cooling by extracting external work by an atmospheric suction type load blower, is blown into the lower tower 8a through the conduit 18. However, when this air is extracted from the lower column 8b as a nitrogen-rich gas, it is introduced into the impure nitrogen line 21 without being blown into the upper column 8a. The oxygen, nitrogen, and impure nitrogen thus separated and purified in the upper column 8a are transferred to conduits 19, 20, and 21, respectively.
The air is extracted from the air and sent to the switching heat exchanger 6, where it undergoes heat exchange with the raw material air as described above to recover the temperature to room temperature, and then is taken out as a product.
In particular, the oxygen is pressurized from the conduit 22 by a compressor not shown, and then recovered as product oxygen. The system diagram shown in FIG. 2 shows another conventional method, and the feature of this conventional method is that when the external mechanical energy generated when driving the expansion turbine 17 is recovered, power generation is used instead of the load blower 17a. The main point is that it is directly connected to the machine 17b to recover power. However, the reduction in the power consumption unit (hereinafter referred to as O 2 unit) for obtaining product oxygen for the expansion turbine 17 in each of the conventional processes described above has a limit in the following points. This is because power is saved not directly by reducing the turbine capacity itself, but by the very inefficient indirect method of energy conversion and recovery.
Furthermore, the reduction in O 2 basic unit due to an increase in oxygen yield is not considered at all. Therefore, the present inventors conducted various studies on the possibility of efficiently reducing the O 2 basic unit. In other words, the cooling required to maintain the thermal balance of the air separation system is Q (kcal/h), and the expansion turbine 1
7, the flow rate, adiabatic head, and efficiency are respectively expressed as E(N
m 3 /h), Δiad (kcal/Nm 3 ), and η (%), these variables must satisfy the following equation. Q=E・△iad・η/100...(1) In equation (1), Q is almost uniquely determined once the production amount of the equipment is determined. On the other hand, the O 2 basic unit is directly influenced by the flow rate E of the expansion turbine 17, and reducing E leads to a reduction in the O 2 basic unit. The reason for this is explained below. Also, as shown in Fig. 5, Fig. 4 shows the vapor-liquid equilibrium line and rectification operation line of the upper column. If the amount of raw air supplied to the lower tower is A, and the amount of gas extracted to the expansion turbine is E, then (A-E) is the gas V 1 rising up the lower tower, and the main evaporator converts liquid oxygen into It is evaporated and used to produce rising gas V2 at the bottom of the upper column. As shown in Figure 4, in the lower part of the upper column, rectification is performed according to the operating line a and the equilibrium line, so the rectification conditions are better when the operating line a is away from the equilibrium line, and the O 2 source is The units will get better. Operation line a
The slope of is the descending liquid volume L 2 at the bottom of the upper tower and the rising gas volume V 2
Therefore, in order to improve the O 2 consumption rate, L 2 / V 2 should be made smaller. This is primarily to reduce the flow rate E of the expansion turbine 17. In the present invention, as a means for achieving this, the inlet pressure of the expansion turbine 17 is
By increasing △iad, we succeeded in effectively reducing the flow rate E of the expansion turbine while ensuring the necessary cooling Q for the device. After passing the gaseous air or gaseous nitrogen from the lower tower through the reheating circuit of the main heat exchanger through the circulation heat exchanger and raising the temperature,
The gist is that the pressure is increased by applying it to a load blower of an expansion turbine, and the pressurized air is further cooled by passing through the circulation heat exchanger before being introduced into the expansion turbine. The configuration and effects of the present invention will be explained below based on the drawings of the embodiments. However, the embodiments below are merely representative examples, and the embodiments can be implemented with appropriate changes in accordance with the spirit of the above and below. Needless to say. FIG. 3 shows a system diagram of the all-low-pressure air separation method of the present invention. The basic configuration is the same as that of the conventional example shown in FIGS. 1 and 2, respectively, and the same components are designated by the same reference numerals. and the explanation thereof will be omitted. The following description will focus on the characteristic configuration of this embodiment. A portion of the rising air or nitrogen in the lower tower 8b is transferred to the conduit 1
After being extracted from the heat exchanger 4, it was introduced into the reheat circuit 15 of the switching heat exchanger 6, and after adjusting the intermediate temperature of the switching heat exchanger 6, it was passed through the circulation heat exchanger 25 and raised to room temperature. Thereafter, by applying the load blower 17a of the expansion turbine 17 to recover the external mechanical energy generated by the turbine drive, the expansion turbine 17 is further compressed and the pressure is increased. Then, after cooling the pressurized air by passing it through an aftercooler 24 and a circulation heat exchanger 25,
It is introduced into the expansion turbine 17. Therefore, since the air pressure on the inlet side of the expansion turbine 17 is increased by the recovery of the mechanical energy as compared to the conventional method, the heat drop Δiad caused by the adiabatic expansion also increases accordingly. As a result, the turbine flow rate E
can be reduced within a range that satisfies equation (1), so as mentioned above, the rectification effect in the upper column 8a is enhanced and the product oxygen yield is increased. Furthermore, the expansion turbine 17 can also be made smaller.
Therefore, due to these synergistic effects, the O 2 consumption rate can be significantly reduced. Also, as shown in the diagram, the lower tower 8
Since the rising air from inside b is appropriately heated by the circulation heat exchanger 25 before being introduced into the load blower 17a, it does not particularly hinder the operation of the load blower 17a, and the air passing through the load blower 17a The subsequent pressurized air or nitrogen can be water-cooled in the aftercooler 24, and together with the temperature lowering effect by the circulation heat exchanger 25, the temperature characteristics of the air supplied to the expansion turbine 17 are maintained appropriately. However, installation of the aftercooler 24 is not necessarily required depending on operating conditions. (Example) An example in which the conventional method shown in FIGS. 1 and 2 and the method of the present invention shown in FIG. 3 are applied to an oxygen production apparatus with a production scale of 10,000 Nm 3 is shown below.

【表】【table】

【表】 第1表から明らかな様に、従来方法及び従来
方法におけるタービン流量Eは(タービン流
量/原料空気量)比で約20%であつたものが本発
明方法による場合は約14%となつており、その結
果、膨張タービンのO2原単位は従来方法に比
べて約4.5%減少しており、又従来方法に比べ
て約2.1%減少していることが計算で求められ
る。従つて本発明方法によればランニングコスト
を著しく削減することが可能となり、製品酸素を
より安価に製造できることが明らかである。 尚前述した様に負荷ブロワ17aの出口側と循
環熱交換器25の間にアフタクーラ24を配設す
る場合には逆に該アフタクーラを冷却する為の冷
却水費用分が増加することになるが、この増加分
は上述のO2原単位動力減少分の僅か5〜10%程
度に過ぎないので、たとえアフタクーラを配設し
た場合でもランニングコストの削減効果は十分で
ある。 本発明の空気分離方法は以上の様に構成される
が、要は膨張タービンをいわゆる増圧タービン方
式で駆動すると共に、装置の寒冷を維持し得る範
囲内でタービン流量を積極的に減少せしめて精留
効果即ち製品酸素収率を高めることができるよう
になつた。従つて膨張タービンのO2原単位削減
効果に基づくランニングコストの大巾な節約によ
り、高純度製品酸素はより安価に製造できる様に
なつた。又空気分離装置の運転に要する動力を低
減することによりいわゆる省エネルギー化を図る
ことができるので、エネルギーの節約が強く叫ば
れている今日、こうした面からの産業界に果たす
役割も大きい。
[Table] As is clear from Table 1, the turbine flow rate E in the conventional method and conventional method was approximately 20% (turbine flow rate/feedstock air amount) ratio, but in the method of the present invention, it was approximately 14%. As a result, calculations show that the O 2 consumption rate of the expansion turbine is reduced by about 4.5% compared to the conventional method, and by about 2.1% compared to the conventional method. Therefore, it is clear that according to the method of the present invention, running costs can be significantly reduced and product oxygen can be produced at a lower cost. As mentioned above, when the aftercooler 24 is disposed between the outlet side of the load blower 17a and the circulation heat exchanger 25, the cost of cooling water for cooling the aftercooler will increase. Since this increase is only about 5 to 10% of the above-mentioned reduction in O 2 unit power, the effect of reducing running costs is sufficient even if an aftercooler is provided. The air separation method of the present invention is configured as described above, but the key point is that the expansion turbine is driven by a so-called pressure booster turbine system, and the turbine flow rate is actively reduced within a range that can maintain the cooling of the equipment. It has become possible to increase the rectification effect, that is, the product oxygen yield. Therefore, high-purity product oxygen can now be produced at a lower cost due to significant savings in running costs based on the O 2 consumption reduction effect of expansion turbines. Furthermore, by reducing the power required to operate the air separation device, it is possible to achieve so-called energy saving, so in today's world where there is a strong demand for energy saving, the industry plays a major role in this aspect.

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

第1図及び第2図は従来の酸素製造方法を示す
系統図、第3図は本発明に係る酸素製造方法を例
示する系統図、第4図は上塔についてのX−Y線
図、第5図は精留時の気液状態説明図である。 6……切換式熱交換器、8a……精留塔上塔、
8b……精留塔下塔、17……膨張タービン、1
7a……負荷ブロワ、25……循環熱交換器。
1 and 2 are system diagrams showing the conventional oxygen production method, FIG. 3 is a system diagram illustrating the oxygen production method according to the present invention, and FIG. 4 is an X-Y diagram of the upper column. FIG. 5 is an explanatory diagram of the gas-liquid state during rectification. 6... Switching type heat exchanger, 8a... Rectification column upper column,
8b... Fractionation column lower column, 17... Expansion turbine, 1
7a... Load blower, 25... Circulating heat exchanger.

Claims (1)

【特許請求の範囲】[Claims] 1 主熱交換器によつて低温戻りガスと熱交換し
て冷却した原料空気を精留塔下塔に導入して富酸
素液体空気と富窒素ガスに分離すると共に、該下
塔内を上昇する気体空気又は気体窒素の一部を抜
出して前記主熱交換器の再熱回路を通して中間温
度を調整した後、操業に必要な寒冷を発生する膨
張タービンに導入して膨張せしめ、外部仕事を行
なうことによつて、系の熱平衡を成立させる様に
した空気分離方法において、前記再熱回路を通過
してきた気体空気又は気体窒素を循環熱交換器に
通して昇温した後、前記膨張タービンの負荷ブロ
ワにかけて昇圧し、更に該昇圧空気を前記循環熱
交換器に通して冷却した後、前記膨張タービンに
導入することを特徴とする空気分離方法。
1. Feed air cooled by heat exchange with low-temperature return gas in the main heat exchanger is introduced into the lower column of the rectification column and separated into oxygen-enriched liquid air and nitrogen-rich gas, and the gases rise in the lower column. After extracting a portion of the air or gaseous nitrogen and adjusting the intermediate temperature through the reheat circuit of the main heat exchanger, it is introduced into an expansion turbine that generates the refrigeration necessary for operation and is expanded to perform external work. Therefore, in an air separation method that establishes thermal equilibrium in the system, the gaseous air or gaseous nitrogen that has passed through the reheating circuit is passed through a circulation heat exchanger to raise its temperature, and then passed through the load blower of the expansion turbine. An air separation method characterized in that the pressurized air is pressurized, and the pressurized air is further cooled by passing through the circulation heat exchanger and then introduced into the expansion turbine.
JP13246683A 1983-07-20 1983-07-20 Method of separating air Granted JPS6023771A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP13246683A JPS6023771A (en) 1983-07-20 1983-07-20 Method of separating air
BR8403601A BR8403601A (en) 1983-07-20 1984-07-19 AIR SEPARATION PROCESS
IN525/MAS/84A IN161955B (en) 1983-07-20 1984-07-19

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13246683A JPS6023771A (en) 1983-07-20 1983-07-20 Method of separating air

Publications (2)

Publication Number Publication Date
JPS6023771A JPS6023771A (en) 1985-02-06
JPS6157550B2 true JPS6157550B2 (en) 1986-12-08

Family

ID=15082029

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13246683A Granted JPS6023771A (en) 1983-07-20 1983-07-20 Method of separating air

Country Status (3)

Country Link
JP (1) JPS6023771A (en)
BR (1) BR8403601A (en)
IN (1) IN161955B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6237676A (en) * 1985-08-12 1987-02-18 株式会社神戸製鋼所 Nitrogen generator
JPS62102074A (en) * 1985-10-30 1987-05-12 株式会社日立製作所 Gas separation method and device

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3563046A (en) * 1968-01-05 1971-02-16 Hydrocarbon Research Inc Air separatiin process
IT1019710B (en) * 1974-07-12 1977-11-30 Nuovo Pignone Spa PROCESS AND EQUIPMENT FOR THE PRODUCTION OF HIGH PERCENTAGES OF OS SIGEN AND / OR NITROGEN IN THE LIQUID STATE
JPS55162579A (en) * 1979-06-06 1980-12-17 Nippon Oxygen Co Ltd Purity control of oxygen product for liquifying air separator
US4243575A (en) * 1979-07-25 1981-01-06 General Electric Company Filled thermoplastic resin compositions

Also Published As

Publication number Publication date
IN161955B (en) 1988-03-05
JPS6023771A (en) 1985-02-06
BR8403601A (en) 1985-06-25

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