JPH0692332B2 - Pressure distillation method for methanol plant - Google Patents
Pressure distillation method for methanol plantInfo
- Publication number
- JPH0692332B2 JPH0692332B2 JP60167409A JP16740985A JPH0692332B2 JP H0692332 B2 JPH0692332 B2 JP H0692332B2 JP 60167409 A JP60167409 A JP 60167409A JP 16740985 A JP16740985 A JP 16740985A JP H0692332 B2 JPH0692332 B2 JP H0692332B2
- Authority
- JP
- Japan
- Prior art keywords
- distillation
- gas
- column
- heat source
- methanol
- 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
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
-
- 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
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
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プラントの加圧蒸留法に関し、特に
プラントのエネルギ原単位を改善すべくリフオーマ出口
ガスの加圧蒸留プロセスに於いて新規な熱回収技術を適
用した上記蒸留法に関する。Description: TECHNICAL FIELD The present invention relates to a pressure distillation method for a methanol plant, and more particularly to a novel heat treatment in the pressure distillation process of a refiner outlet gas in order to improve the energy consumption rate of the plant. The present invention relates to the above distillation method to which a recovery technique is applied.
(従来の技術) 蒸留プロセスに於けるエネルギ原単位の改善という観点
より、近年、加圧蒸留により多重効用を利用した各種の
プロセスが検討されている(例えば、Ind.Eng.Chem.Pro
cess Des.Dev.1983,22,175-179、特開昭53-112803号公
報、特開昭56-123926号公報等)。(Prior Art) From the viewpoint of improving the energy consumption rate in the distillation process, in recent years, various processes utilizing multiple effects by pressure distillation have been investigated (for example, Ind.Eng.Chem.Pro.
cess Des. Dev. 1983, 22, 175-179, JP-A-53-112803, JP-A-56-123926, etc.).
しかしながら、これらは、蒸留系内のエネルギ原単位に
ついてのみの検討であり、改質ガスの熱エネルギ利用を
考慮したプラント全体のエネルギ原単位を改善するとい
う検討はなされていなかつた。However, these are only studies on the energy intensity of the distillation system, and no study has been made on improving the energy intensity of the entire plant in consideration of the utilization of the heat energy of the reformed gas.
すなわち、加圧蒸留の採用により、加圧精留塔の塔底温
度が高く、改質ガスの廃熱の低温域がプロセスに回収で
きぬ為、その分高温の熱が必要となり、総合的には最適
でない第3図の如きプロセスが利用されることが多かつ
た。なお、第3図中、12は加圧精留塔、13は常圧精留
塔、14は加圧精留塔改質ガスリボイラ、17は加圧精留塔
水蒸気リボイラ、18は加圧精留塔リフラックスコンデン
サである。That is, by adopting the pressure distillation, the bottom temperature of the pressure rectification column is high, and the low temperature region of the waste heat of the reformed gas cannot be recovered in the process. Often a non-optimal process such as FIG. 3 is utilized. In FIG. 3, 12 is a pressure rectification column, 13 is an atmospheric rectification column, 14 is a pressure rectification column reforming gas reboiler, 17 is a pressure rectification column steam reboiler, and 18 is a pressure rectification column. It is a tower reflux condenser.
そしてこの大量の余剰廃熱により、冷却水流量あるいは
エアクーラ・フアン動力が増加し、さらにエネルギ原単
位を低下させる原因ともなつていた。This large amount of excess waste heat also increased the flow rate of cooling water or the power of the air cooler / fan, which also caused a reduction in the energy consumption rate.
(発明が解決しようとする問題点) 本発明は、このような低位の余剰廃熱を有効利用し、エ
ネルギ原単位の改善を図るもので、メタノールプラント
の加圧蒸留プロセスに於て、リフオーマ出口ガスの熱エ
ネルギを有効に利用し、低位の廃熱を減少させることに
より、プラントのエネルギ原単位を改善する方法と提案
するものである。(Problems to be Solved by the Invention) The present invention is intended to improve the energy consumption rate by effectively utilizing such a low-level surplus waste heat. In the pressure distillation process of a methanol plant, the refiner outlet is used. The present invention proposes a method for improving the energy consumption rate of a plant by effectively utilizing the thermal energy of gas and reducing low-level waste heat.
(問題点を解決するための手段) 本発明は、脱硫された炭化水素原料を、水蒸気により、
8気圧以上の圧力にて接触リフオーミングして得られる
炭素酸化物、水素及びメタノールを含むガスを、圧縮機
にて昇圧し、メタノール合成の原料ガス(改質ガス)と
し、かつメタノール合成工程にて生成される8〜30重量
%の水を含む合成粗メタノールが、初留塔にて、その低
沸点副生物が除去され、続いて常圧塔と加圧塔の2塔か
ら構成された精留部により蒸留される如き改質、合成、
及び、蒸留工程よりなるメタノールプロセスに於て、 (1)初留塔の加熱用熱源としては、改質ガスが初留塔
の塔底温度よりも5〜25℃高い温度(すなわち、70〜11
5℃)まで熱回収されるリボイラより賄われ、 (2)加圧精留塔の加熱用熱源としては、改質ガスが該
精留塔の塔底温度よりも5〜25℃高い温度(すなわち、
135〜225℃)まで熱回収されるリボイラ、及び水蒸気を
熱源とするリボイラより賄われ、 (3)常圧精留塔の加熱用熱源としては、加圧精留塔の
塔頂ガスによる多重効用コンデンサ、及び改質ガスが該
精留塔の塔底温度よりも5〜25℃高い温度(すなわち11
0〜150℃)まで熱回収されるリボイラ、及び必要ならば
水蒸気を熱源とするリボイラにより賄われる、 上記のうち少くとも2つを組み合わせ、改質ガスは塔底
温度の高い塔から低い塔へ直列に流れるようにしたこと
を特徴とする、改質ガスの熱エネルギを有効に回収しプ
ラント全体のエネルギ消費量を減少させることのできる
メタノールプラントの加圧蒸留方法に関する。(Means for Solving Problems) The present invention is a method for producing a desulfurized hydrocarbon raw material by steam.
A gas containing carbon oxide, hydrogen and methanol obtained by catalytic reforming at a pressure of 8 atm or more is pressurized by a compressor to be a raw material gas (reforming gas) for methanol synthesis, and in a methanol synthesis step. The low-boiling-point by-product of the synthetic crude methanol containing 8 to 30% by weight of water is removed in the initial distillation column, and then the rectification is composed of two columns, an atmospheric column and a pressure column. Reforming, synthesis, such as distillation by part
In the methanol process including the distillation step, (1) As a heat source for heating the initial distillation column, the reformed gas is at a temperature 5 to 25 ° C. higher than the bottom temperature of the initial distillation column (that is, 70 to 11).
(2) As a heat source for heating the pressurized rectification column, the reformed gas is a temperature 5 to 25 ° C. higher than the bottom temperature of the rectification column (that is, 5 ° C.). ,
It is covered by a reboiler that recovers heat up to 135 to 225 ° C) and a reboiler that uses steam as a heat source. (3) As a heat source for heating the atmospheric rectification column, multiple effects by top gas of the pressurized rectification column The temperature of the condenser and the reformed gas is 5 to 25 ° C. higher than the bottom temperature of the rectification column (that is, 11
It is covered by a reboiler that recovers heat up to 0 to 150 ° C) and, if necessary, a reboiler that uses steam as a heat source. At least two of the above are combined and the reformed gas flows from a tower with a high bottom temperature to a tower with a low bottom temperature. The present invention relates to a pressurized distillation method for a methanol plant capable of effectively recovering the thermal energy of the reformed gas and reducing the energy consumption of the entire plant, which is characterized in that they flow in series.
本発明によれば、蒸留系外からの熱負荷を最小とする蒸
留プロセスを採用することが、かならずしもプラントの
エネルギ原単位を最小とすることにはならぬことがわか
る。According to the present invention, it is understood that adopting a distillation process that minimizes the heat load from outside the distillation system does not necessarily minimize the energy consumption rate of the plant.
以下、これを具体例に基き説明する。尚、説明はLS/F
(Light-Split/Heat-integration-forward)のプロセス
に基き行うが、本発明はこのLS/Fのみでなく、あらゆる
加圧蒸留プロセスに対し有効である。Hereinafter, this will be described based on a specific example. The explanation is LS / F
Although it is based on the (Light-Split / Heat-integration-forward) process, the present invention is effective not only for this LS / F but also for any pressure distillation process.
なお、LS/Fとは、加圧塔に供給し、塔頂から製品を抜
き、塔底液をその常圧塔に供給し、その塔頂から製品
を、塔底から水を、中間の段から側流を抜出すようなフ
ロー(第1〜3図参照)をいい、1塔目で軽い成分(製
品)の一部を抜き、熱の受授がプロセス流体の流れに対
して順方向である為、LS/Fと呼ぶ。In addition, LS / F is supplied to the pressure tower, the product is removed from the top of the tower, the bottom liquid is supplied to the atmospheric tower, the product is supplied from the top, and the water is supplied from the bottom to the intermediate stage. A side flow is extracted from the column (see Figs. 1 to 3), and a part of the light component (product) is extracted in the first tower, and the transfer of heat is in the forward direction with respect to the flow of the process fluid. Therefore, it is called LS / F.
(1) 比較される2プロセス(従来法と本発明法) 本発明法と従来法における加圧蒸留に於ける改質ガス熱
量の回収フローを第1図と第2図に示す。(1) Two Processes to be Compared (Conventional Method and Present Invention Method) FIG. 1 and FIG. 2 show recovery flows of the reforming gas heat quantity in the pressure distillation in the present invention method and the conventional method.
第2図は、蒸留系外からの熱負荷の最も少ない(すなわ
ち、蒸留のエネルギ原単位の最も小さい)プロセスにお
けるフローである。この熱回収フローは従来の加圧蒸留
に於いてよく用いられるフローであり、以後これを“従
来法”と称する。FIG. 2 is a flow in the process in which the heat load from the outside of the distillation system is the smallest (that is, the energy intensity of distillation is the smallest). This heat recovery flow is a flow often used in conventional pressure distillation, and will be referred to as "conventional method" hereinafter.
従来法では、加圧精留塔12の熱源はリフオーマ出口ガス
(すなわち改質ガス)と蒸気によりリボイラ14,17によ
り賄われ、常圧精留塔13及び初留塔11の熱源は、多重効
用により、加圧精留塔12のリフラツクスコンデンサ18,1
8より与えられている。In the conventional method, the heat source of the pressurized rectification column 12 is covered by the reboiler outlet gas (that is, reformed gas) and steam by the reboilers 14 and 17, and the heat sources of the atmospheric rectification column 13 and the first distillation column 11 have multiple effects. The refraction condenser 18,1 of the pressure rectification column 12
Given by 8.
第1図は、本発明の一例を示すフローである。本発明法
によれば、精留に必要な熱量は従来法より増えるが、低
位の熱回収が増えるために、プラントのエネルギ消費量
は少くなる。以後これを“本発明法”と称する。FIG. 1 is a flow showing an example of the present invention. According to the method of the present invention, the amount of heat required for rectification is increased as compared with the conventional method, but the energy consumption of the plant is reduced due to the increase of the lower heat recovery. Hereinafter, this is referred to as the “method of the present invention”.
本発明法では、初留塔11の加熱用熱源はリフオーマ出口
ガスの廃熱によるリボイラ16により賄われ、加圧精留塔
12は、リボイラ14によるリフオーマ出口ガスの廃筈熱と
リボイラ17による水蒸気をその熱源とし、常圧精留塔13
は、多重効用による加圧精留塔12の塔頂ガス、リフオー
マ出口ガス及び水蒸気によるリボイラ18,15,19によりそ
の熱源が賄われている。なお、第1図中の20は気液分離
器を示している。In the method of the present invention, the heat source for heating the first distillation column 11 is covered by the reboiler 16 by the waste heat of the refumeer outlet gas, and the pressure rectification column is used.
Reference numeral 12 designates an atmospheric pressure rectification column 13 which uses heat generated by the reboiler 14 for exhausting the refumeer outlet gas and steam produced by the reboiler 17 as heat sources.
The heat source is covered by the reboilers 18, 15, and 19 using the overhead gas of the pressurized rectification column 12 with multiple effects, the reformer outlet gas, and steam. In addition, 20 in FIG. 1 has shown the gas-liquid separator.
(2) 総合エネルギ原単位の比較 スチームリフオーマより流出する15気圧の改質ガスの廃
熱を熱源の一部とする2500t/dメタノールのLS/F蒸留プ
ロセスを具体例とし、以下そのエネルギ原単位を、従来
法(第2図)と本発明法(第1図)に基づき比較する。(2) Comparison of total energy intensity A specific example is the LS / F distillation process of 2500 t / d methanol that uses the waste heat of the reformed gas at 15 atm flowing out from the steam reformer as a part of the heat source. The units are compared based on the conventional method (FIG. 2) and the method of the present invention (FIG. 1).
各蒸留塔11〜13のリボイラー14〜17,19熱量及び多重効
用される加圧精留塔12のリフラツクスコンデンサ18熱量
を示したのが第1表である。Table 1 shows the calorific values of the reboilers 14 to 17 and 19 of the distillation columns 11 to 13 and the calorific value of the refraction condenser 18 of the pressure rectification column 12 having multiple effects.
△印は“プロセスに熱を与える(負の消費熱量)”であ
ることを示す。 A mark indicates that "heat is given to the process (negative heat consumption)".
上表より明らかな如く、蒸留系外からの熱負荷、すなわ
ち蒸留のエネルギ消費量だけを比較すると、本発明法よ
りも従来法の蒸留プロセスの方が20.3MMKcal/hだけ優れ
ている。As is clear from the above table, when comparing only the heat load from outside the distillation system, that is, the energy consumption of distillation, the conventional distillation process is superior to the method of the present invention by 20.3 MMKcal / h.
しかしながら各蒸留塔の改質ガス及び水蒸気リボイラ熱
量とプロセスには回収されない改質ガスの余剰エネルギ
を示している第2表より明らかな如く、本発明法では、
改質ガスの低温廃熱が効果的に利用されたことにより、
水蒸気リボイラの熱量は逆に18.7MMKcal/hr少くなつて
いる。さらに、本発明法では、従来、余剰廃熱として回
収されなかつた熱量が39.0MMKcal/hrも少くなり、冷却
水所要量の低下、あるいはエアクーラのフアン動力の低
下をもたらす。However, as is clear from Table 2 which shows the reformed gas and steam reboiler calories of each distillation column and the surplus energy of the reformed gas that is not recovered in the process, in the method of the present invention,
By effectively utilizing the low temperature waste heat of the reformed gas,
On the contrary, the calorific value of the steam reboiler is reduced by 18.7MMKcal / hr. Furthermore, in the method of the present invention, the amount of heat that has not been recovered as excess waste heat in the past is reduced by 39.0 MMKcal / hr, which leads to a decrease in the required amount of cooling water or a decrease in the fan power of the air cooler.
以上のように、本発明法は、従来法と比し、蒸留原単位
だけ比べれば劣つているものの、総合的には改質ガス熱
量を効果的に回収することができ、省エネルギ型のプロ
セスとなつていることがわかる。 As described above, the method of the present invention is inferior to the conventional method when compared with the distillation basic unit, but it is possible to effectively recover the calorific value of the reformed gas as a whole, and an energy-saving process. You can see that
尚、第1図のフローは、本発明に基くプロセスの一例で
あり、蒸留系の加圧度、改質系の圧力や熱回収法によ
り、3つの改質ガスリボイラ14〜16のうちの1つを省く
ことも可能である。The flow of FIG. 1 is an example of the process based on the present invention, and one of the three reformed gas reboilers 14 to 16 is selected depending on the degree of pressurization of the distillation system, the pressure of the reforming system and the heat recovery method. It is also possible to omit.
また、第1図のフローにおいて、改質ガスリボイラ16の
後流側(すなわち、改質ガスの合成系へ至るラインの途
上)に脱気器給水予熱器(図示省略)を設置してもよい
が、該予熱器の熱量は従来法、本発明法において同量
(例えば第1表の場合いずれも15.0MMKcal/hr)であ
る。Further, in the flow of FIG. 1, a deaerator feedwater preheater (not shown) may be installed on the downstream side of the reformed gas reboiler 16 (that is, on the way to the reformed gas synthesis system). The heat quantity of the preheater is the same in the conventional method and the method of the present invention (for example, in the case of Table 1, both are 15.0 MMKcal / hr).
第1図は本発明蒸留プロセスの一例を示すフロー図、第
2図及び第3図は多重効用を利用した加圧蒸留に於いて
従来よく使用されるフローの一例を示す図である。FIG. 1 is a flow chart showing an example of the distillation process of the present invention, and FIGS. 2 and 3 are diagrams showing an example of a flow often used conventionally in pressure distillation utilizing multiple effects.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 守田 和裕 東京都千代田区丸の内2丁目5番1号 三 菱重工業株式会社内 (72)発明者 村山 勝利 新潟県新潟市松浜町3500番地 (72)発明者 橋本 修 新潟県新潟市松浜町3500番地 (56)参考文献 特開 昭53−79807(JP,A) 特開 昭53−112803(JP,A) 特開 昭55−45637(JP,A) 特開 昭56−123926(JP,A) 特公 昭56−16338(JP,B1) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Kazuhiro Morita 2-5-1, Marunouchi, Chiyoda-ku, Tokyo Sanryo Heavy Industries Co., Ltd. (72) Inventor Masaru Murayama 3500 Matsuhama-cho, Niigata-shi, Niigata (72) Inventor Osamu Hashimoto 3500, Matsuhama-cho, Niigata City, Niigata (56) Reference JP-A-53-79807 (JP, A) JP-A-53-112803 (JP, A) JP-A-55-45637 (JP, A) JP-A-SHO 56-123926 (JP, A) JP-B 56-16338 (JP, B1)
Claims (1)
り、8気圧以上の圧力にて接触リフォーミングして得ら
れる炭素酸化物、水素及びメタンを含むガスを、圧縮機
にて昇圧し、メタノール合成の原料ガス(改質ガス)と
し、かつメタノール合成工程にて生成される8〜30重量
%の水を含む合成粗メタノールが、初留塔にて、その低
沸点副生物が除去され、続いて常圧塔と加圧塔の2塔か
ら構成された精留部により蒸留される如き改質、合成、
及び蒸留工程よりなるメタノールプロセスに於て、 (1) 初留塔の加熱用熱源としては、改質ガスが初留
塔の塔底温度よりも5〜25℃高い温度(すなわち、70〜
115℃)まで熱回収されるリボイラにより賄われ、 (2) 加圧精留塔の加熱用熱源としては、改質ガスが
該精留塔の塔底温度よりも5〜25℃高い温度(すなわ
ち、135〜225℃)まで熱回収されるリボイラ、及び水蒸
気を熱源とするリボイラにより賄われ、 (3) 常圧精留塔の加熱用熱源としては、加圧精留塔
の塔頂ガスによる多重効用コンデンサ、及び改質ガスが
該精留塔の塔底温度よりも5〜25℃高い温度(すなわ
ち、110〜150℃)まで熱回収されるリボイラ、及び必要
ならば水蒸気を熱源とするリボイラにより賄われる、 上記のうち少くとも2つを組み合わせ、改質ガスは塔底
温度の高い塔から低い塔へ直列に流れるようにしたこと
を特徴とする、改質ガスの熱エネルギを有効に回収しプ
ラント全体のエネルギ消費量を減少させることのできる
メタノールプラントの加圧蒸留方法。1. A gas containing carbon oxide, hydrogen and methane obtained by contact reforming a desulfurized hydrocarbon raw material with steam at a pressure of 8 atm or more is pressurized with a compressor to produce methanol. The raw crude gas (reforming gas) for synthesis, and synthetic crude methanol containing 8 to 30% by weight of water produced in the methanol synthesis step, had its low boiling point by-products removed in the first distillation column, followed by Reforming, synthesis, such as distillation by a rectification section composed of two columns, an atmospheric pressure column and a pressure column,
In a methanol process consisting of a distillation step, (1) As a heat source for heating the first distillation column, the reformed gas is at a temperature 5 to 25 ° C higher than the bottom temperature of the first distillation column (that is, 70 to
(2) As a heat source for heating the pressurized rectification column, the reformed gas is 5 to 25 ° C. higher than the bottom temperature of the rectification column (ie , 135 to 225 ° C), and a reboiler that uses steam as a heat source. (3) As a heat source for heating the atmospheric rectification column, multiple gas is used by the top gas of the pressurized rectification column. By the effect condenser, and the reboiler in which the reformed gas is heat-recovered to a temperature 5 to 25 ° C. higher than the bottom temperature of the rectification column (that is, 110 to 150 ° C.), and if necessary, a reboiler using steam as a heat source. It is provided that at least two of the above are combined to allow the reformed gas to flow in series from a tower with a high bottom temperature to a tower with a low bottom temperature, which effectively recovers the thermal energy of the reformed gas. The energy consumption of the entire plant can be reduced. Pressure distillation method methanol plants.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60167409A JPH0692332B2 (en) | 1985-07-31 | 1985-07-31 | Pressure distillation method for methanol plant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60167409A JPH0692332B2 (en) | 1985-07-31 | 1985-07-31 | Pressure distillation method for methanol plant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6229539A JPS6229539A (en) | 1987-02-07 |
| JPH0692332B2 true JPH0692332B2 (en) | 1994-11-16 |
Family
ID=15849157
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60167409A Expired - Lifetime JPH0692332B2 (en) | 1985-07-31 | 1985-07-31 | Pressure distillation method for methanol plant |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0692332B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115671774A (en) * | 2022-10-26 | 2023-02-03 | 中石化南京工程有限公司 | Refining device and method for preparing methanol product by carbon dioxide hydrogenation |
| CN117398709B (en) * | 2023-10-27 | 2026-04-21 | 濮阳市联众兴业化工有限公司 | Distillation column for separating crude alcohol as a byproduct of coal-to-methanol production |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5016338A (en) * | 1973-06-18 | 1975-02-20 | ||
| GB1592949A (en) * | 1976-12-22 | 1981-07-15 | Ici Ltd | Methanol |
| IN148355B (en) * | 1977-03-11 | 1981-01-24 | Ici Ltd | |
| JPS5545637A (en) * | 1978-09-28 | 1980-03-31 | Continental Oil Co | Methanol plant |
| JPS56123926A (en) * | 1980-03-06 | 1981-09-29 | Toyo Eng Corp | Purification of methanol |
-
1985
- 1985-07-31 JP JP60167409A patent/JPH0692332B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6229539A (en) | 1987-02-07 |
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