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JP2006307134A - Method for separating C2 + fraction from light gas containing NOx - Google Patents

Method for separating C2 + fraction from light gas containing NOx Download PDF

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JP2006307134A
JP2006307134A JP2005256506A JP2005256506A JP2006307134A JP 2006307134 A JP2006307134 A JP 2006307134A JP 2005256506 A JP2005256506 A JP 2005256506A JP 2005256506 A JP2005256506 A JP 2005256506A JP 2006307134 A JP2006307134 A JP 2006307134A
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gas
fraction
phase component
demethanizer
methane
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JP4814588B2 (en
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Yoshinori Ota
好則 太田
Tatsuhiko Kushino
達彦 串野
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Mitsubishi Chemical Corp
Research Association of Refinery Integration for Group Operation
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Research Association of Refinery Integration for Group Operation
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    • 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
    • F25J3/0204Processes 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 characterised by the feed stream
    • F25J3/0219Refinery gas, cracking gas, coke oven gas, gaseous mixtures containing aliphatic unsaturated CnHm or gaseous mixtures of undefined nature
    • 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
    • F25J3/0228Processes 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 characterised by the separated product stream
    • F25J3/0233Processes 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 characterised by the separated product stream separation of CnHm with 1 carbon atom or more
    • 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
    • F25J3/0228Processes 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 characterised by the separated product stream
    • F25J3/0238Processes 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 characterised by the separated product stream separation of CnHm with 2 carbon atoms or more
    • 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
    • F25J3/0228Processes 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 characterised by the separated product stream
    • F25J3/0252Processes 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 characterised by the separated product stream separation of hydrogen
    • 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
    • F25J2200/00Processes or apparatus using separation by rectification
    • F25J2200/74Refluxing the column with at least a part of the partially condensed overhead gas
    • 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
    • F25J2205/00Processes or apparatus using other separation and/or other processing means
    • F25J2205/02Processes or apparatus using other separation and/or other processing means using simple phase separation in a vessel or drum
    • F25J2205/04Processes or apparatus using other separation and/or other processing means using simple phase separation in a vessel or drum in the feed line, i.e. upstream of the fractionation step
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
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    • 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
    • F25J2210/00Processes characterised by the type or other details of the feed stream
    • F25J2210/02Multiple feed streams, e.g. originating from different sources
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    • 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
    • F25J2210/00Processes characterised by the type or other details of the feed stream
    • F25J2210/12Refinery or petrochemical off-gas
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    • 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
    • F25J2215/00Processes characterised by the type or other details of the product stream
    • F25J2215/62Ethane or ethylene
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    • F25J2270/00Refrigeration techniques used
    • F25J2270/90External refrigeration, e.g. conventional closed-loop mechanical refrigeration unit using Freon or NH3, unspecified external refrigeration
    • 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
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    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P30/00Technologies relating to oil refining and petrochemical industry
    • Y02P30/40Ethylene production

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  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Mechanical Engineering (AREA)
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  • General Engineering & Computer Science (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Separation By Low-Temperature Treatments (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

【課題】 FCCオフガス等のNOx含有軽質ガスについて、NOxガムの生成・堆積を抑制しながら、C2+留分を分離・回収する。
【解決手段】 水素、メタン及びC2+を含む原料を気相成分と液相成分とに分離する気液分離槽31〜34と、該気相成分を水素留分と低圧メタン留分に分離する水素・低圧メタン分離槽51と、該液相成分を蒸留し、液相成分をC2+留分として分離する脱メタン塔61と、脱メタン塔61の塔頂成分を冷却し、気相成分を高圧メタン留分として、液相成分の一部を中圧メタン留分として分離し、残りを脱メタン塔61に還流する還流槽71と、気液分離槽31〜34からの気相成分を水素留分及び低圧・中圧・高圧メタン留分と熱交換して冷却する深冷熱交換器41とを備えた深冷系1において、NOx含有軽質ガスをNOx含有軽質ガス蒸留塔62に供給して蒸留し、得られた気相成分を脱メタン塔61に供給する。
【選択図】 図2
A for NO x containing light gases such as FCC off-gas, while suppressing the generation and accumulation of the NO x gums, to separate and recover C2 + fraction.
SOLUTION: Gas-liquid separation tanks 31 to 34 for separating a raw material containing hydrogen, methane and C2 + into a gas phase component and a liquid phase component, and hydrogen for separating the gas phase component into a hydrogen fraction and a low pressure methane fraction A low-pressure methane separation tank 51, a demethanizer 61 for distilling the liquid phase component and separating the liquid phase component as a C2 + fraction, a top component of the demethanizer 61 is cooled, and a gas phase component is converted to high pressure methane. As a fraction, a part of the liquid phase component is separated as a medium pressure methane fraction, and the remainder is refluxed to the demethanizer 61, and the gas phase components from the gas-liquid separation tanks 31 to 34 are separated into hydrogen fractions. and in cryogenic system 1 that includes a deep cold heat exchanger 41 for cooling by heat exchange low-medium pressure and high pressure methane fraction, and supplies the NO x containing light gas to NO x containing light gas distillation column 62 The vapor phase component obtained by distillation is supplied to the demethanizer 61.
[Selection] Figure 2

Description

本発明は、石油精製プロセス等のFCC工程において副生するFCCオフガス等のNOx含有軽質ガスから、エチレン、プロピレン等の有用オレフィン留分を含むC2+留分を分離する方法に関する。 The present invention is, from the NO x containing light gases such as FCC off-gas by-produced in the FCC process, such as oil refining process, ethylene, relates to a method of separating the C2 + fraction containing useful olefinic cut such as propylene.

石油精製プロセス等の流動接触分解(Fluid Catalytic Cracking:これを適宜「FCC」という。)工程において副生するFCCオフガスには、エチレン、プロピレン等の有用オレフィン留分を含む炭素数2以上の炭化水素(これを適宜「C2+留分」という。以下の記載では、炭素数n以上の炭化水素を、その下限炭素数nを付して「Cn+留分」と呼ぶものとする。)が含まれている。   The FCC off-gas produced as a by-product in the fluid catalytic cracking (Fluid Catalytic Cracking: this is referred to as “FCC” as appropriate) processes such as petroleum refining processes are hydrocarbons containing 2 or more carbon atoms containing useful olefin fractions such as ethylene and propylene (This is appropriately referred to as “C2 + fraction”. In the following description, hydrocarbons having a carbon number of n or more are referred to as “Cn + fraction” with the lower limit of carbon number n attached thereto). Yes.

具体的に、FCC装置から生成したオフガスは、まず(i)副生ガス回収系において、硫化水素などの不純物が除去されるとともに、C3+留分の一部が分離され、水素含有軽質ガス(水素、メタン、C2+留分等を含む。)となる。続いて(ii)脱水・深冷系において、水素と一部のメタンが分離され、軽質ガス(メタン、C2+留分等を含む。)となる(非特許文献1参照)。本明細書においては、FCC装置から生成したオフガスから上述の(i)副生ガス回収系及び(ii)脱水・深冷系を経て得られる軽質ガスを、「FCCオフガス」というものとする。   Specifically, the off-gas generated from the FCC device is first (i) in the by-product gas recovery system, impurities such as hydrogen sulfide are removed and a part of the C3 + fraction is separated to produce a hydrogen-containing light gas (hydrogen , Methane, C2 + fraction, etc.). Subsequently, (ii) in the dehydration / deep cooling system, hydrogen and a part of methane are separated and become light gas (including methane, C2 + fraction, etc.) (see Non-Patent Document 1). In the present specification, a light gas obtained from the off-gas generated from the FCC apparatus through the above-mentioned (i) by-product gas recovery system and (ii) dehydration / deep cooling system is referred to as “FCC off-gas”.

このFCCオフガスをエチレン製造プラントの圧縮工程に供給することにより、有用オレフィン留分を分離・回収することが提案されている(非特許文献2参照)。   It has been proposed to separate and recover useful olefin fractions by supplying this FCC offgas to the compression process of an ethylene production plant (see Non-Patent Document 2).

「石油精製プロセス」、2003年、(株)講談社発行、(社)石油学会編、p.154“Petroleum Refining Process”, 2003, published by Kodansha, edited by The Japan Petroleum Institute, p. 154 Chemical Engineering、1996年11月、p.133〜135Chemical Engineering, November 1996, p. 133-135

しかしながら、FCCオフガスには、メタンやC2+留分の他に、窒素酸化物(これを適宜「NOx」という。)も含まれている。これをそのままエチレン製造プラントの圧縮工程に供給すると、その後段に設けられる精製工程の深冷系(これは上述した石油精製プロセスに設けられる「脱水・深冷系」とは異なるものである。本明細書において単に「深冷系」と言う場合には、石油精製プロセスの「脱水・深冷系」ではなく、エチレン製造プラントの精製工程の深冷系に代表される本発明の適用対象となる深冷系を指すものとする。)において、NOxが爆発性のあるガム(以下、「NOxガム」と称することがある。)を形成し、これが深冷系に堆積してしまうおそれがある。 However, the FCC off-gas contains nitrogen oxide (this is referred to as “NO x ” as appropriate) in addition to methane and C2 + fraction. If this is supplied as it is to the compression step of the ethylene production plant, it is different from the deep cooling system of the refining process provided in the subsequent stage (this is different from the “dehydration / deep cooling system” provided in the oil refining process described above. In the specification, when simply referring to “deep cooling system”, it is not the “dehydration / deep cooling system” of the petroleum refining process, but the application object of the present invention represented by the deep cooling system of the refining process of the ethylene production plant. is intended to refer to cryogenic system in.), gums NO x is in explosive (hereinafter, may be referred to as "NO x gums".) is formed, possibly this will be deposited in the deep cooling system is there.

これに対して、上述の非特許文献2では、アルカリ洗浄や脱水等の手法により、FCCオフガス中のNOxの濃度を100ppb程度まで減少させてから、エチレン製造プラントの圧縮工程に供給するという方策が提案されている。 Measures contrast, in Non-Patent Document 2 described above, by a technique such as alkali washing and dewatered, after decreasing concentrations of the NO x in FCC off-gas to about 100 ppb, of supplying to the compressing process of ethylene production plant Has been proposed.

しかし、FCCオフガスのNOx濃度を低減した場合でも、FCCオフガス中にNOxが僅かでも残存していると、これをエチレン製造プラントの圧縮工程に持ち込んだ場合に、後段の精製工程の深冷系においてNOxガムが生成・堆積するおそれがある。よって、NOxガムの生成・堆積をより確実に抑制しながら、FCCオフガスから有用オレフィン留分を分離・回収する方法が求められていた。 However, even when reduced concentration of NO x FCC offgas, the NO x in FCC off-gas is left, even slightly, when this brought to the compression process of ethylene production plant, the subsequent purification step cryogenic There is a risk that NO x gum is generated and deposited in the system. Therefore, while more reliably suppress the generation and accumulation of the NO x gums, a method of separating and recovering useful olefinic cut from an FCC off-gas has been demanded.

なお、以上の説明においては、石油精製プロセス等のFCCオフガスを有用オレフィン留分を分離・回収する場合を例として説明したが、この場合に限らず、一般にメタン、C2+留分及びNOxを含有するガス(これを適宜「NOx含有軽質ガス」という。)からC2+留分を分離・回収する場合において、同様の課題が広く生じることになる。 In the above description, a case of separating and recovering useful olefinic cut the FCC off-gas and petroleum refining process has been described as an example, not limited to this case, generally containing methane, C2 + fraction and NO x In the case where the C2 + fraction is separated and recovered from the gas to be used (this is referred to as “NO x- containing light gas” as appropriate), the same problem is widely caused.

本発明は、上記課題に鑑みてなされたものである。即ち、本発明の目的は、FCCオフガス等のNOx含有軽質ガスについて、NOxガムの生成・堆積を抑制しながら、C2+留分を分離・回収する方法を提供することにある。 The present invention has been made in view of the above problems. It is an object of the present invention, the NO x containing light gases such as FCC off-gas, while suppressing the generation and accumulation of the NO x gum is to provide a method for separating and recovering C2 + fraction.

本発明者らは鋭意検討の結果、深冷系の気液分離槽における極低温域(約−160℃)の存在が、NOxガムの生成・堆積の原因となっていることに着目した。そして、脱メタン塔の前段に別の蒸留塔(NOx含有軽質ガス蒸留塔)を設け、NOx含有軽質ガスをこのNOx含有軽質ガス蒸留塔で蒸留し、液相成分と気相成分とに分離するとともに、得られた気相成分を深冷系の脱メタン塔に供給するように構成することによって、この極低温域を回避することができ、NOXガムの生成・堆積を抑制しながらC2+留分を分離・回収することが可能になるのを見出して、本発明を完成させた。 As a result of intensive studies, the present inventors have focused on the fact that the existence of a cryogenic temperature region (about −160 ° C.) in the cryogenic gas-liquid separation tank causes the generation and deposition of NO x gum. Then, another distillation column (NO x containing light gas distillation column) provided in front of the demethanizer, and distilled NO x containing light gas in the NO x containing light gas distillation column, a liquid phase component and gaseous component while separated by configured to provide to the demethanizer cryogenic system the gas phase component obtained, it is possible to avoid this extremely low temperature region, to suppress the generation and accumulation of the NO X gum However, it was found that the C2 + fraction could be separated and recovered, and the present invention was completed.

すなわち、本発明の要旨は、メタン、炭素数2以上の炭化水素(以下「C2+」という。)、及び窒素酸化物を含有するガス(以下「NOx含有軽質ガス」という。)から、C2+留分を分離する方法であって、(A)水素、メタン及びC2+を含む原料を供給されて、これを気相成分と液相成分とに分離する気液分離槽と、(B)該気液分離槽により分離された気相成分を、水素留分とメタン留分(以下「低圧メタン留分」という。)とに分離する水素・低圧メタン分離槽と、(C)該気液分離槽により分離された液相成分を蒸留し、液相成分をC2+留分として分離する脱メタン塔と、(D)該脱メタン塔の塔頂成分を冷却し、気相成分をメタン留分(以下「高圧メタン留分」という。)として分離するとともに、液相成分のうち一部をメタン留分(以下「中圧メタン留分」という。)として更に分離し、残りを該脱メタン塔に還流する還流槽と、(E)該気液分離槽により分離された気相成分を、該水素・低圧メタン分離槽により分離された水素留分及び低圧メタン留分、並びに、該還流槽により分離された中圧メタン留分及び高圧メタン留分と熱交換させることにより冷却する深冷熱交換器とを備えた深冷系において、NOx含有軽質ガスをNOx含有軽質ガス蒸留塔に供給して蒸留し、液相成分と気相成分とに分離するとともに、得られた気相成分を該脱メタン塔に供給することにより、NOx含有軽質ガス中のC2+留分を分離するように構成したことを特徴とする、NOx含有軽質ガスからのC2+留分の分離方法に存する(請求項1)。 That is, the gist of the present invention is that C2 + distillation is performed from methane, a hydrocarbon having 2 or more carbon atoms (hereinafter referred to as “C2 +”), and a gas containing nitrogen oxide (hereinafter referred to as “NO x- containing light gas”). (A) a gas-liquid separation tank which is supplied with a raw material containing hydrogen, methane and C2 + and separates it into a gas phase component and a liquid phase component; and (B) the gas-liquid separation method. A hydrogen / low pressure methane separation tank that separates the gas phase component separated by the separation tank into a hydrogen fraction and a methane fraction (hereinafter referred to as “low pressure methane fraction”); and (C) the gas-liquid separation tank. A demethanizer that distills the separated liquid phase component and separates the liquid phase component as a C2 + fraction; and (D) the top component of the demethanizer tower is cooled, and the gas phase component is converted into a methane fraction (hereinafter “ High-pressure methane fraction ”) and a part of the liquid phase components. A further separation as a tan fraction (hereinafter referred to as “medium pressure methane fraction”), the remainder being refluxed to the demethanizer tower, and (E) a gas phase component separated by the gas-liquid separation tank, Chilled heat exchange cooled by heat exchange with the hydrogen and low pressure methane fractions separated by the hydrogen / low pressure methane separation tank, and the medium pressure and high pressure methane fractions separated by the reflux tank In a deep-cooled system equipped with a vessel, the NO x -containing light gas is supplied to a NO x -containing light gas distillation column to be distilled and separated into a liquid phase component and a gas phase component. by supplying the dehydration demethanizer, characterized by being configured to separate the C2 + fraction of the NO x containing light gas, resides in C2 + fraction separation methods from the NO x containing light gas (according Item 1).

本発明によれば、FCCオフガス等のNOx含有軽質ガスをNOx含有軽質ガス蒸留塔で蒸留し、液相成分と気相成分とに分離するとともに、得られた気相成分を深冷系の脱メタン塔に供給するように構成することにより、既存の深冷系の構成を生かしつつ、NOXガムの生成・堆積を抑制しながら、C2+留分を分離することが可能となる。また、NOx含有軽質ガスに含まれるC2+留分を予め取り除いてから脱メタン塔に供給することができるので、脱メタン塔の負荷を低減することが可能になる。また、脱メタン塔に設けられる熱源とNOx含有軽質ガス蒸留塔に設けられる熱源とを異なる温度レベルで制御することができるので、適用するプラントの種類によっては、コストの削減等の効果を得ることも可能になる。 According to the present invention, the NO x containing light gases such as FCC off-gas was distilled NO x containing light gas distillation column, while separated into a liquid phase component and gaseous component, resulting gas phase components of the cryogenic system by configured to supply to the demethanizer, while taking the configuration of an existing cryogenic system, while suppressing the generation and accumulation of the NO X gums, it is possible to separate the C2 + fraction. Further, it is possible to supply to the demethanizer from beforehand remove C2 + fraction contained in NO x containing light gases, it is possible to reduce the load of the demethanizer. Further, it is possible to control the heat source provided in the heat source and the NO x containing light gas distillation column provided demethanizer at different temperature levels, depending on the type of application to the plant, to obtain the effect of reducing such costs It becomes possible.

以下、本発明の実施の形態について詳細に説明するが、本発明は以下の実施の形態に限定されるものではなく、その要旨の範囲内で種々に変更して実施することができる。   Hereinafter, embodiments of the present invention will be described in detail. However, the present invention is not limited to the following embodiments, and various modifications can be made within the scope of the gist of the present invention.

以下の説明では、本発明の実施の形態として、化学プラントの一種であるエチレン製造プラントの精製工程に設けられる、深冷熱交換器及び脱メタン塔を含む系(これを適宜「脱メタン塔まわりの深冷系」或いは単に「深冷系」という。)に対して、本発明を適用した場合を例として説明する。   In the following description, as an embodiment of the present invention, a system including a cryogenic heat exchanger and a demethanizer provided in a purification process of an ethylene production plant that is a kind of chemical plant (this is appropriately referred to as “around the demethanizer tower”). A case where the present invention is applied to “deep cooling system” or simply “deep cooling system”) will be described as an example.

エチレン製造プラントの典型的な構成の例としては、ナフサ等の原料を分解炉にて熱分解する工程(分解工程)と、得られた分解ガスを急冷・精留する工程(急冷工程)と、急冷・精留された分解ガスを圧縮する工程(圧縮工程)と、圧縮された分解ガスを各成分に分離・精製し、主製品であるエチレン、プロピレン等を得る工程(精製工程)とを備えた構成が挙げられる。   As an example of a typical configuration of an ethylene production plant, a process of thermally decomposing raw materials such as naphtha in a cracking furnace (decomposition process), a process of quenching and rectifying the obtained cracked gas (quenching process), It includes a process for compressing the rapidly cooled and rectified cracked gas (compression process) and a process for separating and purifying the compressed cracked gas into its components to obtain ethylene, propylene, etc., which are the main products (purification process) Configuration.

これらのうち、特に精製工程では、先の圧縮工程で圧縮され、水分を完全に除去された分解ガスが、深冷熱交換器にて冷却され、水素留分及び一部のメタン留分(低圧メタン留分)が分離された後、脱メタン塔へフィードされる。脱メタン塔では、塔頂部より残りのメタン留分(中圧メタン留分及び高圧メタン留分)が分離された後、塔底部液は後工程に送られる。後工程では、脱エタン塔、エチレン塔、脱プロパン塔、プロピレン精留塔、脱ブタン塔等の蒸留塔を経由することにより、各成分が分離される。なお、これらの蒸留塔の種類やその順番が異なるプロセスもある。   Of these, particularly in the purification process, the cracked gas that has been compressed in the previous compression process and from which moisture has been completely removed is cooled in a cryogenic heat exchanger, and a hydrogen fraction and a part of the methane fraction (low-pressure methane fraction). The distillate) is separated and fed to a demethanizer tower. In the demethanizer tower, the remaining methane fraction (medium-pressure methane fraction and high-pressure methane fraction) is separated from the top of the tower, and then the liquid at the bottom of the tower is sent to a subsequent process. In the post-process, each component is separated by passing through a distillation tower such as a deethanizer tower, an ethylene tower, a depropanizer tower, a propylene rectification tower, and a debutane tower. There are also processes in which the types and order of these distillation columns are different.

[I.第1実施形態(参考実施形態)]
図1は、本発明に関連する一実施の形態に係るNOx含有軽質ガスからのC2+留分の分離方法を実施するための構成を設けた、エチレンプラントの精製工程における脱メタン塔まわりの深冷系の構成の一例を模式的に示す図である。
[I. First Embodiment (Reference Embodiment)]
FIG. 1 shows the depth around a demethanizer tower in a purification process of an ethylene plant provided with a configuration for carrying out a method for separating a C2 + fraction from a light gas containing NO x according to an embodiment related to the present invention. It is a figure which shows typically an example of a structure of a cold system.

図1に示す深冷系1は、複数の熱交換器21〜25、多段(図では4段)の気液分離槽31〜34、深冷熱交換器41、水素・低圧メタン分離槽51、脱メタン塔61、還流槽71、調節弁81〜88を備えている。   1 includes a plurality of heat exchangers 21 to 25, multistage (four stages in the figure) gas-liquid separation tanks 31 to 34, a cryogenic heat exchanger 41, a hydrogen / low pressure methane separation tank 51, a desorption system. A methane tower 61, a reflux tank 71, and control valves 81 to 88 are provided.

前段(通常は圧縮工程)から送られてくる分解ガスa(以下、この分解ガスaを原料と呼ぶことがある。)は、水素、メタン及び炭素数2以上の炭化水素を含んでいる。この分解ガスaは熱交換器21で冷却され、その一部が凝縮・液化した状態(気液混相流体a’)となって、第1段の気液分離槽31に送られる。   The cracked gas a sent from the previous stage (usually the compression step) (hereinafter, this cracked gas a may be referred to as a raw material) contains hydrogen, methane, and a hydrocarbon having 2 or more carbon atoms. The cracked gas a is cooled by the heat exchanger 21, partly condensed and liquefied (gas-liquid mixed phase fluid a ′), and sent to the first-stage gas-liquid separation tank 31.

第1段の気液分離槽31では、送られてきた気液混相流体a’が液相成分bと気相成分cとに分離され、液相成分bは後述の脱メタン塔61へ送られる(なお、第1段の気液分離槽31から脱メタン塔61への経路上には通常、液相成分bの流量を調節するための流量調節弁81が設けられる。)。一方、気相成分cは深冷熱交換器41に送られて冷却され、更に熱交換器22により冷却され、その一部が凝縮・液化した状態(気液混相流体c’)となって、第2段の気液分離槽32に送られる。   In the first-stage gas-liquid separation tank 31, the gas-liquid mixed phase fluid a ′ sent is separated into a liquid phase component b and a gas phase component c, and the liquid phase component b is sent to a demethanizer tower 61 described later. (Note that a flow control valve 81 for adjusting the flow rate of the liquid phase component b is usually provided on the path from the first-stage gas-liquid separation tank 31 to the demethanizer 61). On the other hand, the gas phase component c is sent to the cryogenic heat exchanger 41 to be cooled, and further cooled by the heat exchanger 22, and a part thereof is condensed and liquefied (gas-liquid mixed phase fluid c ′). It is sent to the two-stage gas-liquid separation tank 32.

第2段の気液分離槽32では、送られてきた気液混相流体c’が液相成分dと気相成分eとに分離され、液相成分dは後述の脱メタン塔61へ送られる(なお、第2段の気液分離槽32から脱メタン塔61への経路上には通常、液相成分dの流量を調節するための流量調節弁82が設けられる。)。一方、気相成分eは深冷熱交換器41に送られて冷却され、更に熱交換器23により冷却され、その一部が凝縮・液化した状態(気液混相流体e’)となって、第3段の気液分離槽33に送られる。   In the second-stage gas-liquid separation tank 32, the gas-liquid mixed phase fluid c ′ sent is separated into the liquid phase component d and the gas phase component e, and the liquid phase component d is sent to the demethanizer tower 61 described later. (Note that a flow rate adjusting valve 82 for adjusting the flow rate of the liquid phase component d is usually provided on the path from the second stage gas-liquid separation tank 32 to the demethanizer 61). On the other hand, the vapor phase component e is sent to the cryogenic heat exchanger 41 to be cooled, and further cooled by the heat exchanger 23, and a part thereof is condensed and liquefied (gas-liquid mixed phase fluid e ′). It is sent to the three-stage gas-liquid separation tank 33.

第3段の気液分離槽33では、送られてきた気液混相流体e’が液相成分fと気相成分gとに分離され、液相成分fは後述の脱メタン塔61へ送られる(なお第3段の気液分離槽33から脱メタン塔61への経路上には通常、液相成分fの流量を調節するための流量調節弁83が設けられる。)。一方、気相成分gは深冷熱交換器41に送られて冷却され、更に熱交換器24により冷却されて、その一部が凝縮・液化した状態(気液混相流体g’)となって、第4段の気液分離槽34に送られる。   In the third-stage gas-liquid separation tank 33, the gas-liquid mixed phase fluid e ′ sent is separated into the liquid phase component f and the gas phase component g, and the liquid phase component f is sent to the demethanizer tower 61 described later. (Note that a flow rate adjusting valve 83 for adjusting the flow rate of the liquid phase component f is usually provided on the path from the third-stage gas-liquid separation tank 33 to the demethanizer 61). On the other hand, the gas phase component g is sent to the cryogenic heat exchanger 41 to be cooled, and further cooled by the heat exchanger 24, and a part thereof is condensed and liquefied (gas-liquid mixed phase fluid g ′), It is sent to the fourth stage gas-liquid separation tank 34.

第4段(最終段)の気液分離槽34では、送られてきた気液混相流体g’が液相成分hと気相成分iとに分離され、液相成分hは後述の脱メタン塔61へ送られる(なお、第4段の気液分離槽34から脱メタン塔61への経路上には通常、液相成分hの流量を調節するための流量調節弁84が設けられる。)。一方、気相成分iは深冷熱交換器41に送られて冷却され、その一部が凝縮・液化した状態(気液混相流体i’)となって、水素・低圧メタン分離槽51に送られる。   In the gas-liquid separation tank 34 in the fourth stage (final stage), the gas-liquid mixed phase fluid g ′ sent is separated into a liquid phase component h and a gas phase component i, and the liquid phase component h is a demethanizer tower described later. (In addition, a flow rate adjusting valve 84 for adjusting the flow rate of the liquid phase component h is usually provided on the path from the fourth stage gas-liquid separation tank 34 to the demethanizer 61). On the other hand, the gas phase component i is sent to the cryogenic heat exchanger 41 to be cooled, and a part thereof is condensed and liquefied (gas-liquid mixed phase fluid i ′) and sent to the hydrogen / low pressure methane separation tank 51. .

水素・低圧メタン分離槽51では、送られてきた気液混相流体i’が液相成分jと気相成分kとに分離される。気相成分j(主に水素からなる。)は、水素留分として深冷熱交換器41に送られ、冷媒として用いられる。一方、液相成分g(主にメタンからなる。)は、流量調節弁85にてフラッシュされて圧力と温度を低下させられた上で、低圧メタン留分として深冷熱交換器41に送られ、やはり冷媒として用いられる。   In the hydrogen / low pressure methane separation tank 51, the gas-liquid mixed phase fluid i ′ sent is separated into a liquid phase component j and a gas phase component k. The gas phase component j (mainly composed of hydrogen) is sent to the cryogenic heat exchanger 41 as a hydrogen fraction and used as a refrigerant. On the other hand, the liquid phase component g (mainly composed of methane) is flushed by the flow control valve 85 to reduce the pressure and temperature, and then sent to the deep heat exchanger 41 as a low-pressure methane fraction. It is also used as a refrigerant.

脱メタン塔61では、気液分離槽31〜34から送られてきた液相成分b,d,f,hが蒸留されるとともに、塔底よりC2+留分lが分離され、後工程ヘとフィードされる。また、脱メタン塔61の塔頂から分離された成分(塔頂成分)mは、塔頂コンデンサ(熱交換器)25に送られて冷却され、その一部が凝縮・液化した状態(気液混相流体m’)となって、還流槽71に送られて気液分離される。分離された液相成分の一部nは、還流液として脱メタン塔61へ還流される(なお、還流槽71から脱メタン塔61への経路上には通常、還流液nの流量を調節するための流量調節弁86が設けられる。)。液相成分の残りo(主にメタンからなる。)は、流量調節弁87でフラッシュされ、圧力と温度を低下させられて、中圧メタン留分として深冷熱交換器41に送られ、冷媒として用いられる。また、還流糟71で分離された気相成分p(主にメタンからなる。)は、高圧メタン留分として深冷熱交換器41に送られ、やはり冷媒として用いられる(なお、還流槽71から深冷熱交換器41への経路上には通常、高圧メタン留分pの流量を調節するための流量調節弁88が設けられる。)。   In the demethanizer 61, the liquid phase components b, d, f, and h sent from the gas-liquid separation tanks 31 to 34 are distilled, and the C2 + fraction l is separated from the bottom of the tower and fed to the subsequent process. Is done. In addition, the component (top component) m separated from the top of the demethanizer 61 is sent to the top condenser (heat exchanger) 25 to be cooled and partially condensed / liquefied (gas-liquid). The mixed phase fluid m ′) is sent to the reflux tank 71 for gas-liquid separation. A part n of the separated liquid phase component is refluxed as a reflux liquid to the demethanizer tower 61 (note that the flow rate of the reflux liquid n is usually adjusted on the path from the reflux tank 71 to the demethanizer tower 61. A flow control valve 86 is provided for this purpose). The remainder o (mainly composed of methane) of the liquid phase component is flushed by the flow rate control valve 87, the pressure and temperature are lowered, and sent to the chilled heat exchanger 41 as an intermediate pressure methane fraction, as a refrigerant. Used. In addition, the gas phase component p (mainly composed of methane) separated in the reflux tank 71 is sent to the chilled heat exchanger 41 as a high-pressure methane fraction, and is also used as a refrigerant (note that it is used as a refrigerant from the reflux tank 71). A flow rate adjusting valve 88 for adjusting the flow rate of the high-pressure methane fraction p is usually provided on the path to the cold heat exchanger 41.)

更に、図1に示す深冷系1には、本実施形態の分離方法を実施するための構成要素として、脱メタン塔61にNOx含有軽質ガス(図中の符号x)を供給する経路が備えられるとともに、その経路上に流量調節弁91及び熱交換器92が設けられる。 Further, the cryogenic system 1 shown in FIG. 1 has a path for supplying NO x -containing light gas (symbol x in the figure) to the demethanizer 61 as a component for carrying out the separation method of the present embodiment. A flow rate adjusting valve 91 and a heat exchanger 92 are provided on the path.

NOx含有軽質ガスとしては、上述の様に、メタン、C2+留分及びNOxを含有するガスであれば、その種類は特に制限されない。例としては、やはり上述の様に、石油精製プロセスのFCCオフガスが挙げられる。 As described above, the NO x -containing light gas is not particularly limited as long as it is a gas containing methane, a C2 + fraction and NO x . An example is FCC off-gas in an oil refining process, again as described above.

外部から供給されたNOx含有軽質ガスは、まず、脱メタン塔61に供給される。好ましくは、NOx含有軽質ガスは、脱メタン塔61の塔内組成とほぼ同じ値になるような位置に供給される。また、脱メタン塔61に供給される前には、脱メタン塔61の供給位置における温度、圧力がほぼ同じ値となるように、NOx含有軽質ガスの圧力・温度が調整される。したがって、NOx含有軽質ガスは、必要に応じて、圧縮機や調節弁91による圧力調整或いは流量調整、及び熱交換器92による冷却もしくは加熱が行なわれる。なお、図1では前述のように、調節弁91及び熱交換器92を備えた例を示しているが、この構成に制限される訳ではない。 The NO x -containing light gas supplied from the outside is first supplied to the demethanizer 61. Preferably, the NO x -containing light gas is supplied to a position where the NOx-containing light gas has almost the same value as the composition in the demethanizer 61. Further, before being supplied to the demethanizer 61, the pressure and temperature of the NO x -containing light gas are adjusted so that the temperature and pressure at the supply position of the demethanizer 61 are substantially the same value. Therefore, the NO x -containing light gas is subjected to pressure adjustment or flow rate adjustment by the compressor or the control valve 91 and cooling or heating by the heat exchanger 92 as necessary. In addition, although the example provided with the control valve 91 and the heat exchanger 92 is shown in FIG. 1 as mentioned above, it is not necessarily restricted to this structure.

具体的に、脱メタン塔61の圧力は通常2.5〜3.5MPaG程度、温度は塔底付近が通常−10℃〜10℃程度、塔頂付近が−110℃〜−90℃程度である。   Specifically, the pressure of the demethanizer 61 is usually about 2.5 to 3.5 MPaG, and the temperature is usually about −10 ° C. to 10 ° C. near the tower bottom and about −110 ° C. to −90 ° C. near the top of the tower. .

圧力・温度の調整後、脱メタン塔61に供給されたNOx含有軽質ガスは、気液分離槽31〜34により得られた液相成分b,d,f,hとともに、脱メタン塔61において蒸留されるとともに、塔底よりC2+留分lが分離される。 After adjusting the pressure and temperature, the NO x -containing light gas supplied to the demethanizer 61 and the liquid phase components b, d, f, and h obtained by the gas-liquid separation tanks 31 to 34 in the demethanizer 61. While being distilled, C2 + fraction l is separated from the bottom of the column.

ここで、従来の技術と本実施形態とを比較すると、上述の非特許文献2に代表される従来の技術では、前段である圧縮工程にNOx含有軽質ガスを導入しているので、前段から送られてくる分解ガスa中にNOxが含有され、これが気液分離槽31〜34及び水素・低圧メタン分離槽51を経由することになる。気液分離槽31〜34及び水素・低圧メタン分離槽51の槽内温度は後段に進むにつれて低温となり、水素・低圧メタン分離槽51(最終段)に至っては、その槽内温度が通常−165℃程度の極低温域となる("Reporton Activities of the NOx in Ethylene Recovery Task Group", D. C. Grenoble, Prepared for Presentation at the 2004 Spring AlChE National Meeting, April 25-29, New Orleans, LA参照)。これに対して、NOxガムは通常温度が低いほど生成しやすくなるため、分解ガスa中にNOxが微量でも存在していれば、水素・低圧メタン分離槽51(最終段)においてNOxガムが生成するおそれがある。 Here, when comparing the conventional technique with this embodiment, in the conventional technique represented by the above-mentioned Non-Patent Document 2, since the NO x- containing light gas is introduced into the compression process which is the previous stage, The cracked gas a sent contains NO x , which passes through the gas-liquid separation tanks 31 to 34 and the hydrogen / low-pressure methane separation tank 51. The in-vessel temperatures of the gas-liquid separation tanks 31 to 34 and the hydrogen / low-pressure methane separation tank 51 become lower as the process proceeds to the subsequent stage, and in the hydrogen / low-pressure methane separation tank 51 (final stage), the in-vessel temperature is usually −165. It becomes extremely low temperature range of about ℃ (see "Reporton Activities of the NOx in Ethylene Recovery Task Group", DC Grenoble, Prepared for Presentation at the 2004 Spring AlChE National Meeting, April 25-29, New Orleans, LA). In contrast, NO x because gum made usually easily generated as the temperature is low, if the NO x during the decomposition gas a is present in trace amounts, NO in the hydrogen-pressure methane separation vessel 51 (the final stage) x There is a risk of gum formation.

これに対して、本実施形態の深冷系1によれば、NOx含有軽質ガスは流量調節弁91及び熱交換器92による圧力・温度の調整後、脱メタン塔61に直接供給されるため、気液分離槽31〜34及び水素・低圧メタン分離槽51(特に極低温域である最終段の水素・低圧メタン分離槽51)を通過することがない。NOxが通過する可能性のある経路中、最も低温となるのは調節弁87でフラッシュされた後の中圧メタンであるが、これは上述した様に通常−140℃〜−120℃程度であり、上記水素・低圧メタン分離槽51と比較して高いため、NOxガムの生成・堆積が大幅に抑制される。従って、本実施形態の深冷系1によれば、NOxガムの生成・堆積を抑制しながらC2+留分を分離・回収することが可能になる。 On the other hand, according to the cryogenic system 1 of the present embodiment, the NO x -containing light gas is directly supplied to the demethanizer 61 after adjusting the pressure and temperature by the flow rate control valve 91 and the heat exchanger 92. The gas-liquid separation tanks 31 to 34 and the hydrogen / low-pressure methane separation tank 51 (particularly, the final stage hydrogen / low-pressure methane separation tank 51 in a cryogenic region) are not passed. In the path through which NO x may pass, the lowest temperature is the medium pressure methane after being flushed by the control valve 87, and this is usually about −140 ° C. to −120 ° C. as described above. In addition, since it is higher than the hydrogen / low pressure methane separation tank 51, the generation and deposition of NO x gum is greatly suppressed. Therefore, according to the cryogenic system 1 of this embodiment, it is possible to separate and recover C2 + fraction while suppressing the generation and accumulation of the NO x gums.

なお、図1の構成においては、NOx含有軽質ガスが脱メタン塔61に供給される経路上に流量調節弁91及び熱交換器92が設けられていたが、NOx含有軽質ガスの種類や脱メタン塔61の分離性能に応じて、これらの構成要素をそれぞれ複数設けたり、配置を変更したり、省略したりしてもよい。また、この経路上に他の構成要素(例えば気液分離槽等)を設けてもよい。以下、この様な変形を加えた実施形態について説明する。 In the arrangement of FIG. 1, although the flow control valve 91 and heat exchanger 92 is provided on a path NO x containing light gas is supplied to the demethanizer 61, the type of the NO x containing light gas Ya Depending on the separation performance of the demethanizer 61, a plurality of these components may be provided, the arrangement may be changed, or the components may be omitted. Moreover, you may provide another component (for example, gas-liquid separation tank etc.) on this path | route. Hereinafter, an embodiment with such a modification will be described.

[II.第2実施形態(本発明の実施の形態)]
図2は、本発明の一実施の形態に係るNOx含有軽質ガスからのC2+留分の分離方法を実施するための構成を設けた、エチレンプラントの精製工程における脱メタン塔まわりの深冷系の構成の一例を模式的に示す図である。図2において、図1と同じ構成要素については同一の符号を付して表わしている。
[II. Second Embodiment (Embodiment of the Present Invention)]
FIG. 2 is a cryogenic system around a demethanizer tower in a purification process of an ethylene plant, which is provided with a configuration for carrying out a method for separating a C2 + fraction from a light gas containing NO x according to an embodiment of the present invention. It is a figure which shows typically an example of a structure of. 2, the same components as those in FIG. 1 are denoted by the same reference numerals.

図2の深冷系1’は、図1の深冷系1と同様、複数の熱交換器21〜25、多段(図では4段)の気液分離槽31〜34、深冷熱交換器41、水素・低圧メタン分離槽51、脱メタン塔61、還流槽71、調節弁81〜88を備えている。これらの機能については図1と同様であるので、その説明は省略する。   2 is a plurality of heat exchangers 21 to 25, multistage (four stages in the figure) gas-liquid separation tanks 31 to 34, and a deep cold heat exchanger 41. , A hydrogen / low pressure methane separation tank 51, a demethanizer 61, a reflux tank 71, and control valves 81-88. Since these functions are the same as those in FIG. 1, the description thereof is omitted.

また、図2の深冷系1’においては、NOx含有軽質ガスが脱メタン塔61に供給される経路上に別の蒸留塔(NOx含有軽質ガス蒸留塔、NOx含有軽質ガスストリッパ)62が設けられる。NOx含有軽質ガスは、まずこのNOx含有軽質ガスストリッパ62に供給されて蒸留される。NOx含有軽質ガスストリッパ62の塔頂より得られた気相成分(主にメタン留分)qは脱メタン塔61に送られて、各気液分離槽31〜34によって得られた液相成分b,d,f,hとともに蒸留される。一方、NOx含有軽質ガスストリッパ62の塔底からはC2+留分rが抜き出され、脱メタン塔61により得られたC2+留分lとともに後工程ヘとフィードされる。 In the cryogenic system 1 ′ of FIG. 2, another distillation column (NO x- containing light gas distillation column, NO x- containing light gas stripper) is provided on the path through which the NO x- containing light gas is supplied to the demethanizer 61. 62 is provided. The NO x -containing light gas is first supplied to the NO x -containing light gas stripper 62 and distilled. The gas phase component (mainly methane fraction) q obtained from the top of the NO x -containing light gas stripper 62 is sent to the demethanizer 61 and the liquid phase components obtained by the gas-liquid separation tanks 31 to 34. Distilled with b, d, f, h. On the other hand, the C2 + fraction r is extracted from the bottom of the NO x -containing light gas stripper 62 and fed to the subsequent process together with the C2 + fraction l obtained by the demethanizer 61.

こうした構成によって、NOx含有軽質ガスに含まれるC2+留分をNOx含有軽質ガスストリッパ62で予め取り除いてから脱メタン塔61に供給することができるので、脱メタン塔の負荷を低減することが可能になる。また、脱メタン塔61に設けられる熱源とNOx含有軽質ガスストリッパ62に設けられる熱源とを異なる温度レベルで制御することができるので、適用するプラントの種類によっては、コストの削減等の効果を得ることも可能になる。 By such configuration, the C2 + fraction contained in NO x containing light gas can be supplied after removing in advance the demethanizer 61 in NO x containing light gas stripper 62, it is possible to reduce the load of the demethanizer It becomes possible. In addition, since the heat source provided in the demethanizer 61 and the heat source provided in the NO x -containing light gas stripper 62 can be controlled at different temperature levels, an effect such as cost reduction can be obtained depending on the type of plant to be applied. It can also be obtained.

[III.第3実施形態(参考実施形態)]
図3は、本発明に関連する一実施の形態に係るNOx含有軽質ガスからのC2+留分の分離方法を実施するための構成を設けた、エチレンプラントの精製工程における脱メタン塔まわりの深冷系の構成の一例を模式的に示す図である。図3において、図1及び図2と同じ構成要素については同一の符号を付して表わしている。
[III. Third Embodiment (Reference Embodiment)]
FIG. 3 shows the depth around the demethanizer tower in the purification process of an ethylene plant provided with a configuration for carrying out a method for separating a C2 + fraction from a light gas containing NO x according to an embodiment related to the present invention. It is a figure which shows typically an example of a structure of a cold system. In FIG. 3, the same components as those in FIGS. 1 and 2 are denoted by the same reference numerals.

図3の深冷系1”は、図2の深冷系1’と同様、複数の熱交換器21〜25、多段(図では4段)の気液分離槽31〜34、深冷熱交換器41、水素・低圧メタン分離槽51、脱メタン塔61、NOx含有軽質ガスストリッパ62、還流槽71、調節弁81〜88を備えている。これらの機能については図1及び図2と同様であるので、その説明は省略する。 3 is similar to the refrigeration system 1 ′ of FIG. 2, a plurality of heat exchangers 21 to 25, multistage (four stages in the figure) gas-liquid separation tanks 31 to 34, and a refrigeration heat exchanger. 41, hydrogen-pressure methane separation tank 51, demethanizer 61, NO x containing light gas stripper 62, a reflux tank 71, and a regulating valve 81 to 88. these features similar to FIG. 1 and FIG. 2 Since there is, explanation is omitted.

また、図3の深冷系1”においては、第1段の気液分離槽31により得られた液相成分bが、まずNOx含有軽質ガスストリッパ62に供給され、NOx含有軽質ガスと一緒に蒸留される。その後は図2の深冷系1’と同様、NOx含有軽質ガスストリッパ62の塔頂より得られた気相成分(主にメタン留分)qは、脱メタン塔61に送られて、各気液分離槽31〜34によって得られた液相成分b,d,f,hとともに蒸留される。一方、NOx含有軽質ガスストリッパ62の塔底からはC2+留分rが抜き出され、脱メタン塔61により得られたC2+留分lとともに後工程ヘとフィードされる。 In the refrigeration system 1 ″ of FIG. 3, the liquid phase component b obtained by the first-stage gas-liquid separation tank 31 is first supplied to the NO x -containing light gas stripper 62, and the NO x -containing light gas and After that, the vapor phase component (mainly methane fraction) q obtained from the top of the NO x -containing light gas stripper 62 is removed from the demethanizer 61 as in the case of the refrigeration system 1 ′ of FIG. sent to each gas-liquid liquid phase component b obtained by separation tank 31 to 34, d, f, is distilled together with h. on the other hand, from the bottom of the NO x containing light gas stripper 62 C2 + fraction r Is extracted and fed to the subsequent process together with the C2 + fraction l obtained by the demethanizer 61.

こうした構成によって、NOx含有軽質ガスの組成、温度、圧力等の変動に伴う脱メタン塔61及びNOx含有軽質ガスストリッパ62の動作条件の変動を少なくすることができる。即ち、深冷系1”の属するプラント(例えばエチレンプラント)と異なるプラント(例えば石油精製プラント)からNOx含有軽質ガス(例えばFCCオフガス)が供給される状況において、石油精製プラントの都合によりFCCオフガスの供給が停止した場合等でも、エチレンプラント側では、NOx含有軽質ガスストリッパ62に気液分離槽からの液相成分の供給が続けられているので、NOx含有軽質ガスストリッパ62の動作を継続することができる。従って、エチレンプラントが石油精製プラントの運転条件の変動から受ける影響を低減することが可能となる。 By such configuration, the composition of the NO x containing light gases, temperature, can be reduced variations in operating conditions of the demethanizer 61 and NO x containing light gas stripper 62 due to the variation of the pressure and the like. That is, in a situation where NO x containing light gas (for example, FCC offgas) is supplied from a plant (for example, an oil refinery plant) different from the plant (for example, an ethylene plant) to which the cryogenic system 1 ″ belongs, FCC offgas is used for the convenience of the oil refinery plant. even or when the supply is stopped, and so the ethylene plant side, the supply of the liquid phase component from the gas-liquid separation tank NO x containing light gas stripper 62 is continuing, the operation of the NO x containing light gas stripper 62 Therefore, it is possible to reduce the influence of the ethylene plant from fluctuations in the operating conditions of the oil refinery plant.

なお、図3の深冷系1”においては、第1段の気液分離槽31により得られた液相成分bの全部がNOx含有軽質ガスストリッパ62に供給される構成となっていたが、液相成分bの全部ではなく一部のみをNOx含有軽質ガスストリッパ62に供給し、液相成分bの残りについては図1の深冷系1と同様、脱メタン塔61に直接供給するように構成してもよい。また、第1段の気液分離槽31以外の気液分離槽32〜34により得られた液相成分d,f,hをNOx含有軽質ガスストリッパ62に供給するように構成することも可能である。 In the cryogenic system 1 ″ of FIG. 3, the entire liquid phase component b obtained by the first-stage gas-liquid separation tank 31 is supplied to the NO x -containing light gas stripper 62. In addition, only a part of the liquid phase component b, but not all, is supplied to the NO x -containing light gas stripper 62, and the rest of the liquid phase component b is supplied directly to the demethanizer 61 as in the case of the cryogenic system 1 in FIG. may be configured to. the supply liquid phase component d obtained by the gas-liquid separation tank 32 to 34 other than the gas-liquid separation tank 31 of the first stage, f, and h to the NO x containing light gas stripper 62 It is also possible to configure so as to.

[IV.その他]
以上、本発明の実施形態及び関連する実施形態として、図1〜3に示す深冷系1,1’,1”について説明したが、本発明の適用は図1〜3に示す深冷系1,1’,1”に限られるものではなく、その趣旨を超えない限りにおいて任意の深冷系に適用することができる。
[IV. Others]
As described above, as the embodiment of the present invention and related embodiments, the deep cooling system 1, 1 ′, 1 ″ shown in FIGS. 1 to 3 has been described. , 1 ′, 1 ″, and can be applied to any deep cooling system as long as it does not exceed the gist.

例えば、図1〜3では、上述の様に、気液分離槽31〜34が4段の場合について説明したが、気液分離槽の段数が異なっていてもよい。この場合も、前段から送られてくる気液混相流体が各段の気液分離槽において分離され、液相成分は脱メタン塔へと送られる一方で、気相成分は深冷熱交換器(及び熱交換器)によって冷却され、その一部が凝縮・液化した状態(気液混相流体)で、次段の気液分離槽に(最終段の気液分離槽の場合には、水素・低圧メタン分離槽に)送られるように構成される。また、単一段の気液分離槽の場合も同様に、前段から送られてくる気液混相流体である分解ガス(原料)が分離するとともに、液相成分は脱メタン塔へと送られる一方で、気相成分は深冷熱交換器(及び熱交換器)によって冷却され、その一部が凝縮・液化した状態(気液混相流体)で、水素・低圧メタン分離槽に送られるように構成される。   For example, although FIGS. 1-3 demonstrated the case where the gas-liquid separation tanks 31-34 were four steps as mentioned above, the number of stages of a gas-liquid separation tank may differ. Also in this case, the gas-liquid mixed phase fluid sent from the previous stage is separated in the gas-liquid separation tank of each stage, and the liquid phase component is sent to the demethanizer tower, while the gas phase component is sent to the refrigeration heat exchanger (and It is cooled by a heat exchanger, and a part of it is condensed and liquefied (gas-liquid mixed phase fluid), and it is transferred to the next-stage gas-liquid separation tank (in the case of the last-stage gas-liquid separation tank, hydrogen / low-pressure methane) Configured to be sent to a separation tank). Similarly, in the case of a single-stage gas-liquid separation tank, cracked gas (raw material), which is a gas-liquid mixed phase fluid sent from the previous stage, is separated and the liquid phase component is sent to the demethanizer tower. The gas phase component is cooled by a deep cold heat exchanger (and a heat exchanger), and a part of the gas phase component is condensed and liquefied (gas-liquid mixed phase fluid) and is sent to a hydrogen / low pressure methane separation tank. .

なお、気液分離槽の段数が異なる場合も、最終段の気液分離槽の槽内温度(単段の場合にはその槽内温度)は通常−165℃程度の極低温域となる("Report on Activities of the NOx in Ethylene Recovery Task Group", D. C. Grenoble, Prepared for Presentation at the 2004 Spring AlChE National Meeting, April 25-29, New Orleans, LA参照)。従って、本発明の適用により同様の効果を得ることができる。   In addition, even when the number of stages of the gas-liquid separation tank is different, the temperature in the tank of the gas-liquid separation tank in the final stage (in the case of a single stage, the temperature in the tank) is usually an extremely low temperature range of about −165 ° C. (“ Report on Activities of the NOx in Ethylene Recovery Task Group ", DC Grenoble, Prepared for Presentation at the 2004 Spring AlChE National Meeting, April 25-29, New Orleans, LA). Therefore, the same effect can be obtained by applying the present invention.

また、図1〜3では、深冷熱交換器41及び各段の気液分離槽31〜34のまわりに熱交換器21〜24が設けられているが、熱交換器の数や配置等は任意である。例えば、各段の気液分離槽間において、一部の熱交換器が省かれていても良く、複数の熱交換器が設けられていても良い。   Moreover, in FIGS. 1-3, although the heat exchangers 21-24 are provided around the cryogenic heat exchanger 41 and the gas-liquid separation tanks 31-34 of each stage, the number, arrangement | positioning, etc. of a heat exchanger are arbitrary. It is. For example, some heat exchangers may be omitted between the gas-liquid separation tanks of each stage, and a plurality of heat exchangers may be provided.

また、図1〜3では、気液分離槽31〜34により得られた気体成分c,e,g,iが全て単一の深冷熱交換器41により冷却される構成となっているが、複数の深冷熱交換器が設けられて、これらの気体成分c,e,g,iが別個に冷却されるように構成される場合もある。例えば、最終段以外の気液分離槽31〜33により得られた気体成分c,e,gを冷却する第1の深冷熱交換器と、最終段の気液分離槽34により得られた気体成分iを冷却する第2の深冷熱交換器とを、別個独立に設ける構成等が挙げられる。   1 to 3, the gas components c, e, g, and i obtained from the gas-liquid separation tanks 31 to 34 are all cooled by a single deep heat exchanger 41. In other cases, the gas components c, e, g, and i may be separately cooled. For example, a gas component obtained by the first deep-cooling heat exchanger that cools the gas components c, e, and g obtained by the gas-liquid separation tanks 31 to 33 other than the final stage and the gas-liquid separation tank 34 of the final stage. The structure etc. which provide the 2nd deep-cooling heat exchanger which cools i separately independently are mentioned.

なお、複数の深冷熱交換器を設ける場合、全ての深冷熱交換器で同じ組み合わせの冷媒を使用してもよいが、深冷熱交換器毎に使用する冷媒の組み合わせを変える場合もある。例えば、上述したように第1及び第2の深冷熱交換器を設ける場合であれば、第1の深冷熱交換器では水素留分i,低圧メタン留分k,中圧メタン留分o,高圧メタン留分pの全てを冷媒として使用する一方で、第2の深冷熱交換器では水素留分i及び低圧メタン留分kのみを冷媒として使用する、等の構成が挙げられる。   In addition, when providing a several deep-cooling heat exchanger, you may use the same combination of refrigerant | coolants with all the deep-cooling heat exchangers, but the combination of the refrigerant | coolant used for every deep-cooling heat exchanger may be changed. For example, if the first and second deep heat exchangers are provided as described above, in the first deep heat exchanger, the hydrogen fraction i, the low pressure methane fraction k, the medium pressure methane fraction o, the high pressure While all of the methane fraction p is used as a refrigerant, the second cryogenic heat exchanger may be configured to use only the hydrogen fraction i and the low-pressure methane fraction k as the refrigerant.

また、図1〜3では、気液分離槽31〜34により得られた液相成分b,d,f,hが何れも脱メタン塔61又はNOx含有軽質ガスストリッパ62へと直接、送られる構成となっているが、これらの液相成分に熱交換等の処理を行なった後で、脱メタン塔61又はNOx含有軽質ガスストリッパ62へと送るように構成される場合もある。例えば、これらの液相成分b,d,f,hの一部又は全部がまず深冷熱交換器41に送られて、深冷熱交換器41の冷媒として使用された上で、熱交換により加熱されたこれらの成分b,d,f,hが脱メタン塔61又はNOx含有軽質ガスストリッパ62へと送られる構成等が挙げられる。 1 to 3, all of the liquid phase components b, d, f, and h obtained by the gas-liquid separation tanks 31 to 34 are directly sent to the demethanizer 61 or the NO x -containing light gas stripper 62. In some cases, these liquid phase components are subjected to treatment such as heat exchange and then sent to the demethanizer 61 or the NO x -containing light gas stripper 62. For example, some or all of these liquid phase components b, d, f, and h are first sent to the cryogenic heat exchanger 41 and used as a refrigerant in the cryogenic heat exchanger 41, and then heated by heat exchange. In addition, a configuration in which these components b, d, f, and h are sent to the demethanizer 61 or the NO x -containing light gas stripper 62 is exemplified.

更には、上述の水素留分i,低圧メタン留分k,中圧メタン留分o,高圧メタン留分p,気液分離槽31〜34の液相成分b,d,f,h等の他に、別の流体を深冷熱交換器41等の冷媒として使用する構成としても良い。また、この深冷熱交換器41等において、他の流体を併せて冷却する構成としても良い。   Furthermore, in addition to the hydrogen fraction i, the low-pressure methane fraction k, the medium-pressure methane fraction o, the high-pressure methane fraction p, the liquid phase components b, d, f, h of the gas-liquid separation tanks 31 to 34, etc. Moreover, it is good also as a structure which uses another fluid as refrigerant | coolants, such as the deep-cooling heat exchanger 41 grade | etc.,. Moreover, in this deep-cooling heat exchanger 41 grade | etc., It is good also as a structure which cools another fluid collectively.

また、図1〜3では、流量調節弁81〜88等により各メタン留分等の各種流体の流量調整を行なう構成となっているが、これらの流量調節弁の数、配置、調節対象などが適宜変形して実施される場合もある。また、流量調節弁の代わりに液面調節弁等が設けられる場合もある。   Moreover, in FIGS. 1-3, although it has the structure which adjusts the flow volume of various fluids, such as each methane fraction, by the flow control valves 81-88 etc., the number of these flow control valves, arrangement | positioning, the object to be adjusted, etc. In some cases, the method may be appropriately modified. Further, a liquid level control valve or the like may be provided instead of the flow rate control valve.

また、図1〜3では、単一の脱メタン塔61が設けられ、液相成分b,d,f,hは全てこの脱メタン塔61(又はNOx含有軽質ガスストリッパ62)へ送られて蒸留される構成となっているが、複数の脱メタン塔が設けられる場合もある。例えば、図1の構成において、脱メタン塔61の前段に別の脱メタン塔(プレ脱メタン塔)を設け、第1段の気液分離槽31により得られた液相成分bをまずこのプレ脱メタン塔で蒸留し、塔頂から得られた気相成分を脱メタン塔61に送って、他の気液分離槽32〜34によって得られた液相成分d,f,hとともに蒸留する一方で、塔底からC2+留分を抜き出し、これを脱メタン塔61により得られたC2+留分とともに後工程ヘとフィードする構成等が挙げられる。また、図2、図3のように、NOx含有軽質ガスストリッパ62を設ける構成においては、これに加えてプレ脱メタン塔を設けても良く、更にはNOx含有軽質ガスストリッパ62とプレ脱メタン塔とを一体に設けても良い。 1 to 3, a single demethanizer 61 is provided, and all liquid phase components b, d, f, and h are sent to the demethanizer 61 (or the light gas stripper 62 containing NO x ). Although it is configured to be distilled, a plurality of demethanizer towers may be provided. For example, in the configuration of FIG. 1, another demethanizer tower (pre-demethanizer tower) is provided in the front stage of the demethanizer tower 61, and the liquid phase component b obtained by the first-stage gas-liquid separation tank 31 is first added to this pre-methanizer tower 31. While the gas phase component obtained by distillation in the demethanizer tower is sent to the demethanizer tower 61 and distilled together with the liquid phase components d, f, and h obtained by the other gas-liquid separation tanks 32 to 34. Then, a configuration in which a C2 + fraction is extracted from the bottom of the column and is fed to a subsequent process together with the C2 + fraction obtained by the demethanizer 61 is exemplified. In addition, in the configuration in which the NO x -containing light gas stripper 62 is provided as shown in FIGS. 2 and 3, a pre-demethanizer tower may be provided in addition to this, and further, the NO x -containing light gas stripper 62 and the pre-degassing tower may be provided. A methane tower may be provided integrally.

以上のように、エチレンプラントの精製工程における、脱メタン塔まわりの深冷系の構成には、様々な変形例が存在するが、何れの変形例においても、水素,メタン及び炭素数2以上の炭化水素を含む原料を気液分離槽で分離する際に、気相成分を深冷熱交換器によって冷却するとともに、深冷熱交換器の冷媒として、後段で分離された水素留分、低圧メタン留分、中圧メタン留分、高圧メタン留分を用いるように構成されている点では同一である。   As described above, various modifications exist in the structure of the cryogenic system around the demethanizer tower in the refining process of the ethylene plant. In any of these modifications, hydrogen, methane, and a carbon number of 2 or more. When separating the raw material containing hydrocarbons in the gas-liquid separation tank, the vapor phase component is cooled by a deep-cooling heat exchanger, and as a refrigerant of the deep-cooling heat exchanger, a hydrogen fraction and a low-pressure methane fraction separated in the latter stage This is the same in that the medium-pressure methane fraction and the high-pressure methane fraction are used.

そして、以上の何れの変形例においても、深冷系の構成や運転条件、NOx含有軽質ガスの種類等に応じて、適切な変形を加えて本発明を適用すればよい。基本的には、脱メタン塔に対してNOx含有軽質ガスを供給する経路を設ければ、極低温域となる気液分離槽をNOxが通過するのを防ぐことができ、その結果、NOxガムの生成・堆積を抑制しながら、C2+留分を分離・回収することが可能になる。なお、複数段の脱メタン塔が設けられている場合には、何れの脱メタン塔に対してNOx含有軽質ガスを供給する経路を設けてもよい。 In any of the above modifications, the present invention may be applied with appropriate modifications depending on the configuration of the cryogenic system, the operating conditions, the type of the light gas containing NO x , and the like. Basically, if a path for supplying the NO x -containing light gas to the demethanizer tower is provided, it is possible to prevent NO x from passing through the gas-liquid separation tank that is in the extremely low temperature range. while suppressing the generation and accumulation of the NO x gums, it is possible to separate and recover C2 + fraction. When a plurality of demethanizer towers are provided, a route for supplying the NO x -containing light gas to any of the demethanizer towers may be provided.

更に付言すれば、本発明が適用可能な深冷系は、エチレン精製プラントの精製工程における脱メタン塔まわりの深冷系に限定されるものではない。水素,メタン及びC2+留分を含む原料を多段気液分離槽で分離する際に、気相成分を深冷熱交換器によって冷却するとともに、深冷熱交換器の冷媒として、後段で分離された水素留分、低圧メタン留分、中圧メタン留分、高圧メタン留分を用いるように構成された深冷系であれば、各種の化学プラントやその他の様々な分野において用いられる任意の深冷系に、本発明を適用することが可能である。   In addition, the deep cooling system to which the present invention can be applied is not limited to the deep cooling system around the demethanizer tower in the purification process of the ethylene purification plant. When the raw material containing hydrogen, methane, and C2 + fraction is separated in the multistage gas-liquid separation tank, the vapor phase component is cooled by the cryogenic heat exchanger, and the hydrogen fraction separated in the latter stage is used as a refrigerant for the cryogenic heat exchanger. Can be used in various chemical plants and other various fields as long as it is configured to use water, low pressure methane fraction, medium pressure methane fraction, and high pressure methane fraction. The present invention can be applied.

本発明の用途は特に限定されず、NOx含有軽質ガスからC2+留分を分離することが求められる各種の分野に適用することが可能であるが、特に、石油精製プロセスのFCC工程において副生するFCCオフガスから、エチレン、プロピレン等の有用オレフィン留分を分離する際に好適に用いられる。 Applications of the present invention is not particularly limited, but can be applied to various fields in which it is required to separate the C2 + fractions from the NO x containing light gases, in particular, by-product in the FCC process of petroleum refining processes It is suitably used when separating useful olefin fractions such as ethylene and propylene from the FCC offgas.

本発明に関連する一実施の形態に係るNOx含有軽質ガスからのC2+留分の分離方法を実施するための構成を設けた、エチレンプラントの精製工程における脱メタン塔まわりの深冷系の構成の一例を模式的に示す図である。Configuration of a cryogenic system around a demethanizer tower in a purification process of an ethylene plant, provided with a configuration for carrying out a method for separating a C2 + fraction from a light gas containing NO x according to an embodiment related to the present invention FIG. 本発明の一実施の形態に係るNOx含有軽質ガスからのC2+留分の分離方法を実施するための構成を設けた、エチレンプラントの精製工程における脱メタン塔まわりの深冷系の構成の一例を模式的に示す図である。An example of a configuration of a cryogenic system around a demethanizer tower in a purification process of an ethylene plant provided with a configuration for carrying out a method for separating a C2 + fraction from a NO x -containing light gas according to an embodiment of the present invention FIG. 本発明に関連する一実施の形態に係るNOx含有軽質ガスからのC2+留分の分離方法を実施するための構成を設けた、エチレンプラントの精製工程における脱メタン塔まわりの深冷系の構成の一例を模式的に示す図である。Configuration of a cryogenic system around a demethanizer tower in a purification process of an ethylene plant, provided with a configuration for carrying out a method for separating a C2 + fraction from a light gas containing NO x according to an embodiment related to the present invention FIG.

符号の説明Explanation of symbols

1 深冷系
21〜25,92 熱交換器
31〜34 多段気液分離槽
41 深冷熱交換器
51 水素・低圧メタン分離槽
61 脱メタン塔
62 NOx含有軽質ガスストリッパ(NOx含有軽質ガス蒸留塔)
71 還流槽
81〜88,91 調節弁
1 deep cooling system 21~25,92 heat exchanger 31-34 multistage gas-liquid separation tank 41 deep cold heat exchanger 51 the hydrogen-pressure methane separation tank 61 demethanizer 62 NO x containing light gas stripper (NO x containing light gas distillation Tower)
71 Reflux tank 81-88, 91 Control valve

Claims (1)

メタン、炭素数2以上の炭化水素(以下「C2+」という。)、及び窒素酸化物を含有するガス(以下「NOx含有軽質ガス」という。)から、C2+留分を分離する方法であって、
(A)水素、メタン及びC2+を含む原料を供給されて、これを気相成分と液相成分とに分離する気液分離槽と、
(B)該気液分離槽により分離された気相成分を、水素留分とメタン留分(以下「低圧メタン留分」という。)とに分離する水素・低圧メタン分離槽と、
(C)該気液分離槽により分離された液相成分を蒸留し、液相成分をC2+留分として分離する脱メタン塔と、
(D)該脱メタン塔の塔頂成分を冷却し、気相成分をメタン留分(以下「高圧メタン留分」という。)として分離するとともに、液相成分のうち一部をメタン留分(以下「中圧メタン留分」という。)として更に分離し、残りを該脱メタン塔に還流する還流槽と、
(E)該気液分離槽により分離された気相成分を、該水素・低圧メタン分離槽により分離された水素留分及び低圧メタン留分、並びに、該還流槽により分離された中圧メタン留分及び高圧メタン留分と熱交換させることにより冷却する深冷熱交換器とを備えた深冷系において、
NOx含有軽質ガスをNOx含有軽質ガス蒸留塔に供給して蒸留し、液相成分と気相成分とに分離するとともに、得られた気相成分を該脱メタン塔に供給することにより、NOx含有軽質ガス中のC2+留分を分離するように構成した
ことを特徴とする、NOx含有軽質ガスからのC2+留分の分離方法。
A method for separating a C2 + fraction from methane, a hydrocarbon having 2 or more carbon atoms (hereinafter referred to as “C2 +”), and a gas containing nitrogen oxides (hereinafter referred to as “NO x- containing light gas”). ,
(A) a gas-liquid separation tank which is supplied with raw materials containing hydrogen, methane and C2 + and separates the raw material into a gas phase component and a liquid phase component;
(B) a hydrogen / low pressure methane separation tank for separating a gas phase component separated by the gas-liquid separation tank into a hydrogen fraction and a methane fraction (hereinafter referred to as “low pressure methane fraction”);
(C) a demethanizer for distilling the liquid phase component separated by the gas-liquid separation tank and separating the liquid phase component as a C2 + fraction;
(D) The top component of the demethanizer tower is cooled, the gas phase component is separated as a methane fraction (hereinafter referred to as “high pressure methane fraction”), and a part of the liquid phase component is separated into a methane fraction ( Hereinafter referred to as “medium pressure methane fraction”), and a reflux tank for refluxing the remainder to the demethanizer tower;
(E) The gas phase component separated by the gas-liquid separation tank is divided into a hydrogen fraction and a low-pressure methane fraction separated by the hydrogen / low-pressure methane separation tank, and a medium-pressure methane fraction separated by the reflux tank. In a cryogenic system equipped with a cryogenic heat exchanger that cools by exchanging heat with a methane fraction and a high-pressure methane fraction,
By supplying the NO x -containing light gas to the NO x -containing light gas distillation column and distilling it, separating it into a liquid phase component and a gas phase component, and supplying the obtained gas phase component to the demethanizer tower, NO x content is characterized by being configured to separate the C2 + fraction lighter gas, NO x C2 + fraction separation methods from containing light gas.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008128542A (en) * 2006-11-20 2008-06-05 Kashima Oil Co Ltd Method for detecting NOx compounds accumulated in a cryogenic separation facility
CN111704521A (en) * 2020-06-22 2020-09-25 中国科学院过程工程研究所 A kind of olefin reaction product quenching treatment system and quenching treatment method
CN114087849A (en) * 2021-11-25 2022-02-25 北京恒泰洁能科技有限公司 Pyrolysis gas cryogenic separation method

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JPS61189233A (en) * 1985-02-15 1986-08-22 Mitsui Eng & Shipbuild Co Ltd Method of purifying hydrocarbon decomposition product
JPH1053774A (en) * 1996-05-08 1998-02-24 Air Prod And Chem Inc Method for recovering olefin from olefin/hydrogen mixture

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61189233A (en) * 1985-02-15 1986-08-22 Mitsui Eng & Shipbuild Co Ltd Method of purifying hydrocarbon decomposition product
JPH1053774A (en) * 1996-05-08 1998-02-24 Air Prod And Chem Inc Method for recovering olefin from olefin/hydrogen mixture

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008128542A (en) * 2006-11-20 2008-06-05 Kashima Oil Co Ltd Method for detecting NOx compounds accumulated in a cryogenic separation facility
CN111704521A (en) * 2020-06-22 2020-09-25 中国科学院过程工程研究所 A kind of olefin reaction product quenching treatment system and quenching treatment method
CN111704521B (en) * 2020-06-22 2021-10-26 中国科学院过程工程研究所 Quenching treatment system and quenching treatment method for olefin reaction product
CN114087849A (en) * 2021-11-25 2022-02-25 北京恒泰洁能科技有限公司 Pyrolysis gas cryogenic separation method

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