JPH0558412B2 - - Google Patents
Info
- Publication number
- JPH0558412B2 JPH0558412B2 JP60074073A JP7407385A JPH0558412B2 JP H0558412 B2 JPH0558412 B2 JP H0558412B2 JP 60074073 A JP60074073 A JP 60074073A JP 7407385 A JP7407385 A JP 7407385A JP H0558412 B2 JPH0558412 B2 JP H0558412B2
- Authority
- JP
- Japan
- Prior art keywords
- methanol
- rectification column
- pressure
- column
- temperature
- 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 - Lifetime
Links
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 108
- 238000000034 method Methods 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 3
- 238000011084 recovery Methods 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000000446 fuel Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/10—Process efficiency
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はメタノール精留塔の塔頂メタノール蒸
気の有する動力を回収する方法に関する。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for recovering power possessed by methanol vapor at the top of a methanol rectification column.
(従来の技術及び発明が解決しようとする問題
点)
水素と酸化炭素を接触反応させて得られる粗メ
タノールは一般に3〜30wt%の水、及び微量の
副生成物、すなわち高級アルコール類、パラフイ
ン、ケトン類、エーテル類等を含むもので、これ
らの混合溶液から化学工業原料用の高純度メタノ
ール、或いは燃料用のメタノールを得ようとする
場合、精留塔により精留し、目的とする純度のメ
タノールを得るのが一般的である。(Prior Art and Problems to be Solved by the Invention) Crude methanol obtained by the catalytic reaction of hydrogen and carbon oxide generally contains 3 to 30 wt% of water and trace amounts of by-products, such as higher alcohols, paraffin, Contains ketones, ethers, etc., and when trying to obtain high-purity methanol for chemical industrial raw materials or methanol for fuel from a mixed solution of these, it is rectified using a rectification column to obtain the desired purity. It is common to obtain methanol.
この場合、特に化学工業原料用のメタノールを
得ようとするときは微量の不純物を除去する必要
があり、その要求される純度は一層厳しくなる傾
向にある。このようなメタノール精留塔の還流比
は燃料用メタノールの場合0.8〜1.2、化学工業原
料用の場合は1〜3であり、精留塔塔頂から留出
する蒸気の有するエネルギーは莫大なものとな
る。 In this case, especially when trying to obtain methanol for use as a raw material for the chemical industry, it is necessary to remove trace amounts of impurities, and the required purity tends to become more stringent. The reflux ratio of such a methanol rectification tower is 0.8 to 1.2 for methanol for fuel use, and 1 to 3 for methanol for chemical industry raw materials, and the energy contained in the steam distilled from the top of the rectification tower is enormous. becomes.
低温の熱源から動力を回収する方法として、ラ
ンキンサイクルを組合せる方法が知られている。 A method of combining Rankine cycles is known as a method of recovering power from a low-temperature heat source.
しかし、メタノール精留塔の塔頂温度は、通常
塔圧が大気圧程度であるため64〜65℃であり、仮
に塔頂圧力を2〜3気圧に高めたとしても塔頂温
度は80〜94℃である。ランキンサイクルはこの程
度の温度の熱源では極めて経済効率が悪く、従つ
てメタノールの精留塔にこの方法を適用すること
は得策ではない。 However, the top temperature of a methanol rectification column is usually 64 to 65 degrees Celsius because the column pressure is around atmospheric pressure, and even if the top pressure was increased to 2 to 3 atm, the top temperature would be 80 to 94 degrees Celsius. It is ℃. The Rankine cycle is extremely inefficient economically with a heat source of this temperature, and therefore it is not a good idea to apply this method to a methanol rectification column.
(問題点を解決するための手段)
本発明は以上の如き欠点を解消し、メタノール
精留塔の塔頂から得られる低温のメタノール蒸気
からエネレギーを回収するもので、メタノール精
留塔を塔頂圧力2〜10気圧(絶対)で操作し、塔
頂から留出するメタノール蒸気を、そのまま、或
いは更に加熱して膨脹タービンに導入し、これを
0.3〜1.5気圧(絶対)に膨脹せしめることにより
タービンを駆動し動力を発生させ、膨脹後のメタ
ノール蒸気は冷却、凝縮させて精留塔塔頂へ還流
する方法である。(Means for Solving the Problems) The present invention solves the above-mentioned drawbacks and recovers energy from low-temperature methanol vapor obtained from the top of a methanol rectification column. It operates at a pressure of 2 to 10 atmospheres (absolute), and the methanol vapor distilled from the top of the column is introduced into the expansion turbine as it is or after further heating.
In this method, the methanol vapor is expanded to 0.3 to 1.5 atmospheres (absolute) to drive a turbine and generate power, and the expanded methanol vapor is cooled, condensed, and refluxed to the top of the rectification column.
本発明においてメタノール精留塔の塔頂圧力は
2〜10気圧である。 In the present invention, the top pressure of the methanol rectification column is 2 to 10 atm.
この圧力範囲に相当する塔底圧力は130℃〜183
℃となり、従つて塔頂圧力を10気圧以上とすると
きは温度200℃以下の熱源を蒸留塔塔底熱源とし
て使用することが出来ない。200℃以上の熱源は
本発明方法によるよりもより有利に熱回収するこ
とが出来る。又塔頂圧力、2気圧以下では膨脹タ
ービンの回収動力が小さく有利でない。膨脹ター
ビンにおける膨脹圧力は0.3〜1.5気圧が適当であ
る。これは主に凝縮に要する冷却水温により決め
られる。 The bottom pressure corresponding to this pressure range is 130℃~183℃
Therefore, when the top pressure is 10 atm or more, a heat source with a temperature of 200°C or less cannot be used as the bottom heat source of the distillation column. Heat sources with a temperature of 200° C. or higher can be recovered more advantageously than by the method of the present invention. Moreover, if the tower top pressure is less than 2 atmospheres, the recovery power of the expansion turbine will be small and it will not be advantageous. The appropriate expansion pressure in the expansion turbine is 0.3 to 1.5 atmospheres. This is mainly determined by the cooling water temperature required for condensation.
本発明においては精留塔塔頂蒸気をそのまゝ膨
脹タービンに導いても良いが、これを更に加熱し
た後タービンへ導くことが有効である。加熱温度
は飽和温度より50〜150℃程度過熱した状態とす
るのが好ましい。 In the present invention, the steam at the top of the rectifying column may be directly guided to the expansion turbine, but it is effective to further heat it and then guide it to the turbine. The heating temperature is preferably about 50 to 150°C higher than the saturation temperature.
次に本発明を図面により詳細に説明する。 Next, the present invention will be explained in detail with reference to the drawings.
第1図において原料粗メタノールは流路1から
精留塔2の中段に供給される。塔底にはリボイラ
ー3が設けられ、熱源4により加熱される。塔底
液は流路5を経てリボイラーへ導入され、一部は
流路6を通つて系外へ抜き出される。尚副生成物
の一部は側流路7からメタノール、水を同伴し抜
出される。製品メタノールは塔頂或いは塔頂部よ
り少し下のトレイより液状で流路8を通つて系外
へ抜き出される。塔頂から留出したメタノール蒸
気は、流路9を通つて、過熱器10へ導かれ、熱
源11によつて飽和温度より高く過熱され、12
を経て膨脹タービン13へ導入され膨脹し動力を
発生する。 In FIG. 1, raw material crude methanol is supplied from a flow path 1 to the middle stage of a rectification column 2. A reboiler 3 is provided at the bottom of the tower and heated by a heat source 4. The bottom liquid is introduced into the reboiler through channel 5, and a portion is extracted out of the system through channel 6. A part of the by-product is extracted from the side flow path 7 along with methanol and water. The product methanol is extracted in liquid form from the top of the column or from a tray slightly below the top of the column through a channel 8 to the outside of the system. The methanol vapor distilled from the top of the tower is led to a superheater 10 through a flow path 9, superheated to a temperature higher than the saturation temperature by a heat source 11, and
The fuel is then introduced into the expansion turbine 13 and expanded to generate power.
タービンで発生した動力は軸を介して他に伝達
される。膨脹後のメタノール蒸気は流路14を経
て凝縮器15へ導かれ、冷媒16よつて冷却、凝
縮する。凝縮で液化しなかつた極く微量のガスは
流路17から系外へ抜き出される。液化したメタ
ノールは流路18を通り、再び精留塔頂部へ還流
される。 The power generated by the turbine is transmitted to others via the shaft. The expanded methanol vapor is led to a condenser 15 through a flow path 14, where it is cooled and condensed by a refrigerant 16. The extremely small amount of gas that has not been liquefied by condensation is extracted from the system through the flow path 17. The liquefied methanol passes through the flow path 18 and is refluxed again to the top of the rectification column.
(発明の効果)
本発明によればメタノール精留塔塔頂蒸気の有
するエネルギーを効率的に回収することが出来
る。(Effects of the Invention) According to the present invention, the energy possessed by the vapor at the top of the methanol rectification column can be efficiently recovered.
実施例
水20mol%、及び微量の副生成物を含む粗メタ
ノールを予備蒸留塔へ供給し、低沸点の副生成物
を除去した粗メタノールを精留塔へ供給した。Example Crude methanol containing 20 mol % of water and a trace amount of by-products was supplied to a preliminary distillation column, and the crude methanol from which low-boiling-point by-products had been removed was supplied to a rectification column.
精留塔入口に於ける粗メタノールは水22mol%
で、メタノール量として2.605Kg−mol/Hrであ
る。精留塔の塔頂圧力は3.6気圧、塔頂温度100
℃、還流比1.20で操作され、留出メタノール蒸気
量は5730Kg−mol/Hrであり、外に水、エタノ
ール各100molppmを同伴していた。次いで留出蒸
気は過熱器へ導入され、160℃に過熱された後、
圧力調節弁を通つて圧力3.2気圧となり膨脹ター
ビンへ導かれ、タービンを駆動して圧力0.61気
圧、温度74.9℃に膨脹した。この間にタービンの
軸端から6330kw/Hの動力が得られ、それは合
成系の循環動力として利用された。一方タービン
を出たメタノール蒸気は凝縮器へ導入され、冷却
水によつて冷却されて液化し、再び昇圧され塔頂
へ還流された。 Crude methanol at the inlet of the rectification column contains 22 mol% water.
The amount of methanol is 2.605 Kg-mol/Hr. The pressure at the top of the rectification column is 3.6 atm, and the temperature at the top is 100.
℃ and a reflux ratio of 1.20, the amount of distilled methanol vapor was 5730 Kg-mol/Hr, and 100 molppm each of water and ethanol were entrained. The distillate vapor is then introduced into a superheater and heated to 160°C.
Through the pressure control valve, the pressure became 3.2 atmospheres and was led to the expansion turbine, which drove the turbine and expanded to a pressure of 0.61 atmospheres and a temperature of 74.9°C. During this time, 6330kw/H of power was obtained from the shaft end of the turbine, which was used as circulating power for the synthesis system. On the other hand, methanol vapor exiting the turbine was introduced into the condenser, cooled by cooling water, liquefied, pressurized again, and refluxed to the top of the tower.
第1図は本発明プロセスの工程図である。 FIG. 1 is a process diagram of the process of the present invention.
Claims (1)
対)で操作し、塔頂から留出するメタノール蒸気
を、そのまま、或いは更に加熱して膨張タービン
に導入し、これを0.3〜1.5気圧(絶対)に膨張せ
しめることによりタービンを駆動し動力を発生さ
せ、膨張後のメタノール蒸気は冷却、凝縮させて
精留塔塔頂へ還流することを特徴とするメタノー
ル精留塔の動力回収法。1 The methanol rectification column is operated at a top pressure of 2 to 10 atm (absolute), and the methanol vapor distilled from the top of the column is introduced into an expansion turbine as is or after further heating, and is then heated to a pressure of 0.3 to 1.5 atm (absolute). A power recovery method for a methanol rectification column, which is characterized in that the methanol vapor is expanded completely (absolutely) to drive a turbine to generate power, and the expanded methanol vapor is cooled, condensed, and refluxed to the top of the rectification column.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60074073A JPS61233640A (en) | 1985-04-08 | 1985-04-08 | Power recovery method for methanol rectification tower |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60074073A JPS61233640A (en) | 1985-04-08 | 1985-04-08 | Power recovery method for methanol rectification tower |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61233640A JPS61233640A (en) | 1986-10-17 |
| JPH0558412B2 true JPH0558412B2 (en) | 1993-08-26 |
Family
ID=13536634
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60074073A Granted JPS61233640A (en) | 1985-04-08 | 1985-04-08 | Power recovery method for methanol rectification tower |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61233640A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105536279A (en) * | 2015-12-21 | 2016-05-04 | 七台河宝泰隆煤化工股份有限公司 | Rectifying device for methanol |
-
1985
- 1985-04-08 JP JP60074073A patent/JPS61233640A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61233640A (en) | 1986-10-17 |
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