JPS5811916B2 - Coal liquefaction method - Google Patents
Coal liquefaction methodInfo
- Publication number
- JPS5811916B2 JPS5811916B2 JP674977A JP674977A JPS5811916B2 JP S5811916 B2 JPS5811916 B2 JP S5811916B2 JP 674977 A JP674977 A JP 674977A JP 674977 A JP674977 A JP 674977A JP S5811916 B2 JPS5811916 B2 JP S5811916B2
- Authority
- JP
- Japan
- Prior art keywords
- coal
- mixture
- solvent
- pulverized
- acetic acid
- 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
Links
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】
この発明は高温高圧によらず化学的処理、すなわち、固
体石炭を溶剤により酸化させて石炭液化物を生成するこ
とを特徴とする石炭の液化法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a coal liquefaction method characterized by chemical treatment without high temperature and high pressure, that is, by oxidizing solid coal with a solvent to produce a coal liquefied product.
従来、石炭をガソリン、軽油、ペンゾール、フェノール
などの液化炭化水素の生成物に転化する場合、石炭を高
温高圧下で乾留して石炭タールを抽出し、この石炭ター
ルをタール蒸留装置で蒸留分別することで行われるのが
一般であった。Traditionally, when converting coal into liquefied hydrocarbon products such as gasoline, diesel oil, penzole, and phenol, the coal is carbonized under high temperature and pressure to extract coal tar, and this coal tar is distilled and fractionated using a tar distillation device. It was generally done by
しかし、このような乾留による石炭タールの製造技術は
、装置が大型化すると共に石炭タールの放生率も原料炭
の25%にしかならないために石炭の液化率が著しく低
いものとされ、したがって、固体石炭を液化成生物に転
化することは採算面で極めて不利なものとなる。However, with this technology for producing coal tar by carbonization, the equipment becomes large and the release rate of coal tar is only 25% of coking coal, so the liquefaction rate of coal is considered to be extremely low. Converting coal to liquefied organisms is extremely unprofitable.
また、従来においては上述する高圧乾留法の他に、水素
添加法などがあるが、いずれにおいても高温高圧下の処
理工程を必要とするため、経済性に欠は工業化できない
のが現況である。In addition to the above-mentioned high-pressure carbonization method, conventional methods include hydrogenation methods, but all of these methods require processing steps at high temperatures and high pressures, so they are currently uneconomical and cannot be commercialized.
この発明は原料炭のほとんど(約95%)を石炭液化物
化できるようにした石炭の液化法を提供することを目的
とするものであって、破砕した粒状石炭を所要溶剤内に
所定時間浸漬した後、この溶剤の滲透した粒状石炭を乾
燥させ、次にこの乾燥粒状石炭を所望のメツシュに粉砕
すると共に、この微粉状石炭に溶剤を添加して加熱釜に
て所定温度で所望時間煮詰め、石炭液化物を生成するよ
うにしたものである。The purpose of this invention is to provide a coal liquefaction method that can convert most of the coking coal (approximately 95%) into coal liquefaction. After that, the granular coal in which the solvent has permeated is dried, and then this dry granular coal is crushed into a desired mesh, a solvent is added to the pulverized coal, and the pulverized coal is boiled at a predetermined temperature in a heated pot for a desired period of time to form the coal. It is designed to produce a liquefied product.
ここで石炭液化物と称するのは石炭質を酸化させて液状
にしたものを云う。Here, liquefied coal refers to liquefied coal by oxidizing it.
次にこの発明方法の具体例を説明する。Next, a specific example of this invention method will be explained.
まず、褐炭、亜炭、歴青炭等の原料炭をクラッシャ等に
よって3mm程度の小粒に破砕し、この石炭粒を純水と
水酸ナトリウム及びフェノールの混合溶剤とを約10,
000:1の割合にした溶液中に約50時間程度浸漬す
る。First, raw coal such as lignite, lignite, and bituminous coal is crushed into small particles of about 3 mm using a crusher, and the coal particles are mixed with pure water, a mixed solvent of sodium hydroxide, and phenol for about 10 minutes.
000:1 for about 50 hours.
このとき必要に応じ浸漬中の石炭粒を攪伴する。At this time, the coal particles being immersed are stirred if necessary.
次に溶剤の滲透した石炭粒を溶液中から分離捕取し、こ
れを天日あるいは乾燥装置により乾燥させ、石炭粒の崩
壊が容易となる性質にする。Next, the coal particles that have permeated the solvent are separated and collected from the solution, and dried in the sun or with a drying device to make the coal particles easier to disintegrate.
しかる後、上記乾燥石炭粒を製粉機にかけて約150メ
ツシユの微粉体に生成する。Thereafter, the dried coal particles are milled to produce a fine powder of about 150 mesh.
そして純本釣8kgに対し、酢酸のようなカルボン酸お
よびアセトアルデヒドの合剤とエタノールアミンおよび
酢酸の合剤とを4:3に混合した溶剤を7g添加した溶
液中に上記微粉炭を10kg投入して攪伴混合し、これ
を圧力釜等の加熱釜にて一定温度下で所望時間煮詰める
。Then, 10 kg of the above pulverized coal was added to 8 kg of pure fishing rod into a solution in which 7 g of a solvent made by mixing a mixture of carboxylic acid such as acetic acid and acetaldehyde with a mixture of ethanolamine and acetic acid at a ratio of 4:3 was added. The mixture is stirred and mixed, and the mixture is boiled down at a constant temperature for a desired period of time in a heating pot such as a pressure cooker.
この時の熱処理温度は120℃程であり、かつその熱処
理時間は2時間程である。The heat treatment temperature at this time is about 120° C., and the heat treatment time is about 2 hours.
また、この熱処理時間は微粉炭の量により変化すること
は勿論である。Moreover, it goes without saying that the heat treatment time varies depending on the amount of pulverized coal.
このように熱処理されると、石炭質は溶剤により酸化さ
れ、かつタール状に変質して石炭の液化物が生成される
のである。When heat-treated in this manner, the coal is oxidized by the solvent and transformed into a tar-like substance, producing a liquefied coal.
また、この石炭液化物に炭化水素生成物に応じて水素等
を添加すれば、軽油、ペンゾール、ナフタリン等の生成
物に転化することが可能となる。Furthermore, if hydrogen or the like is added to this coal liquefied product depending on the hydrocarbon product, it becomes possible to convert it into products such as light oil, penzole, and naphthalene.
以上のようにこの発明法に依れば、従来のような高圧乾
留法と異なり高温高圧を必要とせず、また、使用する装
置自体が非常に簡単なもので事足りることとなり、さら
に、製造工程も極めて簡易なものとされるから、廉価な
る石炭液化処理が達成化されることとなる。As described above, according to the method of this invention, unlike the conventional high-pressure carbonization method, high temperature and high pressure are not required, and the equipment itself used is very simple.Furthermore, the manufacturing process can be reduced. Since it is considered to be extremely simple, inexpensive coal liquefaction treatment will be achieved.
本発明方法の具体的実施例は下記の通りである。Specific examples of the method of the present invention are as follows.
実施例
褐青炭をクラッシャーに依り3mm程度の小粒に破砕し
、これを純水と水酸ナトリウム及びフェノールの混合溶
剤を約10,000:1の割合で混合した溶液中に約5
0時間浸漬した。Example Lignite coal was crushed into small particles of about 3 mm using a crusher, and this was placed in a solution of about 10,000:1 mixed solvent of pure water, sodium hydroxide, and phenol.
It was soaked for 0 hours.
次に、上記石炭粒を取出し天日にてよく乾燥させた後、
製粉機により150メツシュ程度の微粉炭となした。Next, after taking out the coal grains and drying them well in the sun,
The coal was made into pulverized coal of approximately 150 mesh using a flour mill.
純水8kgに対し酢酸およびアセトアルデヒドの合剤に
エタノールアミンおよび酢酸の合剤とを4:3に混合し
てなる溶剤7gを添加した溶液中に、上記微粉炭1.0
kgを投入し攪伴混合し、これを圧力釜にて120℃程
度の温度で約2時間煮詰めた。1.0 g of the above pulverized coal was added to 8 kg of pure water and 7 g of a solvent made by mixing a mixture of acetic acid and acetaldehyde with a mixture of ethanolamine and acetic acid at a ratio of 4:3.
kg was added and mixed with stirring, and the mixture was boiled down in a pressure cooker at a temperature of about 120° C. for about 2 hours.
これに依り9.50kgの油状物が得られ、石炭の液化
率は約95%であった。As a result, 9.50 kg of oil was obtained, and the liquefaction rate of the coal was approximately 95%.
Claims (1)
ェノールの合剤を添加してなる溶剤内に約50時間程度
浸漬する工程、この浸漬工程で溶剤の滲透した粒状石炭
を乾燥する工程、この乾燥粒状石炭を150メツシュ程
度の微粉に粉砕する製粉工程、この微粉炭10kgに対
し、純本釣8kgに酢酸のようなカルボン酸およびアセ
トアルデヒドの合剤とエタノールアミンおよび酢酸との
合剤を4:3の比率で混合した溶剤7gを混合した溶液
中に混入して120℃程度の温度で加熱処理を施して石
炭液化物を生成する加熱工程とからなる石炭の液化法。1 A step of immersing crushed granular coal in a solvent made by adding a mixture of sodium hydroxide and phenol to pure water for about 50 hours, a step of drying the granular coal that has permeated with the solvent during this immersion step, A milling process in which dry granular coal is pulverized into a fine powder of about 150 mesh.For 10 kg of this pulverized coal, 8 kg of pure fishing rod, a mixture of a carboxylic acid such as acetic acid and acetaldehyde, and a mixture of ethanolamine and acetic acid are added to 4: A coal liquefaction method comprising a heating step of mixing 7 g of a solvent mixed at a ratio of 3:3 into a mixed solution and heating the mixture at a temperature of about 120° C. to generate a coal liquefied product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP674977A JPS5811916B2 (en) | 1977-01-26 | 1977-01-26 | Coal liquefaction method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP674977A JPS5811916B2 (en) | 1977-01-26 | 1977-01-26 | Coal liquefaction method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5392805A JPS5392805A (en) | 1978-08-15 |
JPS5811916B2 true JPS5811916B2 (en) | 1983-03-05 |
Family
ID=11646833
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP674977A Expired JPS5811916B2 (en) | 1977-01-26 | 1977-01-26 | Coal liquefaction method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5811916B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01146720U (en) * | 1988-03-10 | 1989-10-11 | ||
JPH0441712Y2 (en) * | 1983-12-23 | 1992-09-30 | ||
JPH0541322Y2 (en) * | 1986-07-04 | 1993-10-19 |
-
1977
- 1977-01-26 JP JP674977A patent/JPS5811916B2/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0441712Y2 (en) * | 1983-12-23 | 1992-09-30 | ||
JPH0541322Y2 (en) * | 1986-07-04 | 1993-10-19 | ||
JPH01146720U (en) * | 1988-03-10 | 1989-10-11 |
Also Published As
Publication number | Publication date |
---|---|
JPS5392805A (en) | 1978-08-15 |
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