JPS60170693A - Connected process of coal liquefaction process and coke preparation process - Google Patents

Connected process of coal liquefaction process and coke preparation process

Info

Publication number
JPS60170693A
JPS60170693A JP2576384A JP2576384A JPS60170693A JP S60170693 A JPS60170693 A JP S60170693A JP 2576384 A JP2576384 A JP 2576384A JP 2576384 A JP2576384 A JP 2576384A JP S60170693 A JPS60170693 A JP S60170693A
Authority
JP
Japan
Prior art keywords
coal
hydrogen
coal liquefaction
coke oven
coke
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.)
Pending
Application number
JP2576384A
Other languages
Japanese (ja)
Inventor
Yoshitaka Hirayama
精孝 平山
Shoichi Oi
大井 章市
Sadao Wasaka
和坂 貞雄
Shigemi Nagayoshi
永吉 繁已
Hidehiko Sugimura
杉村 秀彦
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
MITSUI SEKITAN EKIKA KK
Original Assignee
MITSUI SEKITAN EKIKA KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by MITSUI SEKITAN EKIKA KK filed Critical MITSUI SEKITAN EKIKA KK
Priority to JP2576384A priority Critical patent/JPS60170693A/en
Priority to IN286/CAL/84A priority patent/IN160158B/en
Publication of JPS60170693A publication Critical patent/JPS60170693A/en
Pending legal-status Critical Current

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  • Coke Industry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

PURPOSE:To obtain a liquefied oil under mild reaction conditions simply, by using a saccharide tar as a solvent for coal liquefaction, and coal obtained from solvent purification as an addition agent for preparation of coke for metallurgy. CONSTITUTION:A coke oven gas evolved from the coke oven 1' is partially used as a fuel for the coke oven 1' and the rest is sent to the hydrogen purifying device 2'. The coke oven gas is blended with hydrogen from the coal liquefying process 3' and a hydrocarbon gas by the device 2', purified and as a hydrogen gas rich is hydrogen for coal liquefaction is sent to a coal liquefaction process. A high-calorie gas rich in hydrocarbon gas prepared as a by-product by the device 2' as a fuel is sent to the coke oven 1' or the coal liquefaction process 3'. Crude tar prepared by the oven 1' is directly fed to the process 3'. In the process 3', coal is liquefied in the presence of a solvent for liquefaction and hydrogen, separated into an exhaust gas, a liquefied oil, coal obtained from solvent purification, and an insoluble substance, and the exhaust gas is returned to the device 2'. The coal obtained from solvent purification is sent to the coke oven 1'.

Description

【発明の詳細な説明】 本発明はコークス製造工程で得られる粗タールとコーク
ス炉ガスを石炭液化工程剤および水素として石炭液化工
程で使用するとともに1石炭液化工程で得られる浴剤精
製炭をコークス炉装入炭中に配合して冶金用コークスを
製造することを特徴とする石炭液化工程−コークス製造
工程結合プロセスに関するものである。
Detailed Description of the Invention The present invention uses crude tar and coke oven gas obtained in the coke manufacturing process as a coal liquefaction process agent and hydrogen, and uses purified coal as a bath agent obtained in the coal liquefaction process for coke. The present invention relates to a combined coal liquefaction process and coke production process characterized in that coke for metallurgical use is produced by blending into coal charged in a furnace.

従来から1石炭液化用水素はろ炭液化工程で生fJy、
するン山の一部を循環使用している。したがって。
Conventionally, hydrogen for 1 coal liquefaction is produced in the filtration coal liquefaction process, fJy,
A portion of Mt.Suruun is reused. therefore.

溶剤の糸外への損失を補なうために石炭准化物から筒状
4で溶剤を回収する必要かあり、必然的に放北条件が厳
しくなり1石炭゛牧化工程の運転費や装置費が高くなる
。そこで、溶剤の系外への損失を補な5方法として、不
足分を石油系浴剤で補な5方法(日本国特許第9960
15 彊) 、コークス炉から得られる粗タールで補な
う方法(特開昭58−93787号)等が知られている
。しかし、これらσ)方法においても大部分の溶剤は石
炭液化工程で生by、する油であるため、液化条件が厳
しく 7’、Cることは避けられない。しかも1石炭液
化工程で生成′1−るl/litを多量に浴剤として循
環使用することは装置K効率を考える上でも好ましくな
い。
In order to compensate for the loss of solvent to the outside of the yarn, it is necessary to recover the solvent from the coal mixture in a cylindrical tube 4, which inevitably leads to severe release conditions and lower operating and equipment costs for the coal pasture process. becomes higher. Therefore, there are 5 methods to compensate for the loss of solvent to the outside of the system.
15), a method of supplementing with crude tar obtained from a coke oven (Japanese Unexamined Patent Publication No. 58-93787), etc. are known. However, even in these σ) methods, most of the solvent is oil produced in the coal liquefaction process, so it is unavoidable that the liquefaction conditions are severe. Moreover, it is not preferable to recirculate a large amount of 1-l/lit produced in one coal liquefaction process as a bath agent, considering the efficiency of the apparatus.

−万2石炭液化用水素は通常1石炭液化物あるいは石炭
欣北用炭の一部ン原料として1石炭ガス化プラントによ
り製造される。このため、カス化プラントを液化プラン
トに併設して建設する必要があり、ガス化プラントの建
設費、運転費及び高価な石炭液化物を原料とする等によ
って1石炭液化工程体の価格がより高価な−ものとなる
- Hydrogen for coal liquefaction is usually produced in a coal gasification plant as a raw material for coal liquefaction or as a part of coal for coal production. For this reason, it is necessary to construct a cassification plant alongside the liquefaction plant, and the price of one coal liquefaction process becomes more expensive due to the construction and operating costs of the gasification plant and the use of expensive coal liquefaction as raw material. It becomes something.

このよ−うに、従来の石炭液化法では石炭液化用浴剤お
よび水素を確保する7こめに多大な費用を安し1石炭液
化の工業化を著しく阻害する原因となっていた。
As described above, in the conventional coal liquefaction method, the cost of securing a bath agent and hydrogen for coal liquefaction is extremely low, which has significantly hindered the industrialization of coal liquefaction.

本発明者らはこれら石炭液化用浴剤および水素の確保に
安する費用を戦減し、浴剤精製炭の収率の高い、より経
済的な石炭液化法を開発丁べく鋭意研兇を重ねた結果1
石炭液化工程とコークス製造工程とを結@′した本発明
を完成するに至った。
The inventors of the present invention have made extensive efforts to develop a more economical coal liquefaction method that reduces the cost of securing bath agents and hydrogen for coal liquefaction and has a high yield of purified coal for bath agents. Result 1
We have completed the present invention, which combines a coal liquefaction process and a coke production process.

即ち1本発明はコークス製造工程で得られる粗タールな
石炭液化用済剤として石炭液化工程で使用するとともに
、コークス炉カスと石炭液化工程からの排カスとの混合
ガスを精製し石炭液化用水素として石炭紙化工程で使用
し1石炭液化工程で得られる浴剤精製炭の全量または一
部をコークス炉装入炭中に配合使用することを特徴とす
る石炭液化工程−コークス製造工侮紹台プロセスである
That is, 1. The present invention is used in the coal liquefaction process as a crude tarry coal liquefaction agent obtained in the coke manufacturing process, and also purifies the mixed gas of coke oven dregs and waste dregs from the coal liquefaction process to produce hydrogen for coal liquefaction. Coal liquefaction process characterized in that all or part of the bath agent refined coal obtained in the coal liquefaction process is blended into the coal charged in the coke oven. It's a process.

A:発明で用いる祖タールとは、机在−叡に用いられて
いる蚕炉式コークス炉あるいは成型コークス製造時に乾
留炉から得られる分留前のコールタールであり、または
分留後のカールボール油、タレオンート油、アントラセ
ン拙ならひにこれら分留前、後の油の混@物の使用も可
能である・また。
A: The raw tar used in the invention is the coal tar before fractional distillation obtained from the coke oven used in the coke oven or the carbonization furnace during the production of molded coke, or the coal tar after fractional distillation. It is also possible to use a mixture of these oils before and after fractional distillation.

コークス炉カスとは、上記コークス炉および乾留炉から
得られる力・スである。
Coke oven scum is the energy obtained from the above-mentioned coke oven and carbonization furnace.

矢に本発明による石炭&1シ工程とコークス製造工程の
結合組合せ方法の一実施態様を第1図に基′づいて説明
する。
An embodiment of the method for combining the coal and coke production process and the coke production process according to the present invention will be described with reference to FIG.

コークス炉1′より出1こコークス炉カスはラインaを
辿って一部はコークス炉の燃料として、残−りは水素精
製装置2′に送られる。水素精製装置2′ではコークス
炉ガスと石炭液化工程3′からラインC乞辿っ−C込ら
れてくる水素と炭化水素ガスを主成分とする排ガスが混
合され、精製されて水素リッチの石炭液化用水素となっ
てラインbを通って石炭液化工程に送られる。また、水
素精製装置2′で副生する炭化水素カスリンチの市カロ
リーガスはラインb′を超って燃料としてコークス炉も
しくは石炭准11Z工程3′に送られる。コークス炉1
′で生成した粗タールはラインdを通って直抜石炭欣化
工程3′に哄粕きれる。ここで徂タールは石炭液化工程
3′で回収訟れる浴剤の一部と混合されて石炭液化用浴
剤として使用することも出来る。(図示ゼすう 石炭液化工程3′では臨青辰、血臨肯炭、褐炭寺の石炭
類が石炭液化用浴剤と水素Q)介在下で液化ぜれ、排カ
ス、7秋化7111.俗剤輔製炭および不浴性wJ賀と
に分l!i11.きれる。分離された排ガスの全短筐1
こはそσS−都はラインCを辿って水素14i製鉄直2
′に戻され、残りは石炭液化用水素の水素濃U調製用ガ
スどし石炭液化工程34′内で循環使用される。
A portion of the coke oven dregs discharged from the coke oven 1' is sent along line a, while a portion thereof is used as fuel for the coke oven, and the remainder is sent to the hydrogen purification device 2'. In the hydrogen refining equipment 2', the coke oven gas, the hydrogen coming from the coal liquefaction process 3' through the line C, and the exhaust gas mainly composed of hydrocarbon gas are mixed and purified to produce hydrogen-rich coal liquefaction. It becomes hydrogen and is sent to the coal liquefaction process through line b. Moreover, the municipal gas of hydrocarbon sludge produced as a by-product in the hydrogen purification apparatus 2' is sent as a fuel to a coke oven or a coal storage 11Z process 3' via a line b'. coke oven 1
The crude tar produced in step ' is passed through line d and sent to the direct coal sludge process 3'. Here, the tar can be mixed with a part of the bath agent recovered in the coal liquefaction step 3' and used as a bath agent for coal liquefaction. (In the illustrated coal liquefaction process 3', Linqingchen, Chilinken coal, and lignite temple coals are liquefied in the presence of a coal liquefaction bath agent and hydrogen Q, and the scum is discharged. Common agent charcoal making and non-bath sex wJ Kato! i11. I can do it. Complete short housing for separated exhaust gas 1
Kohaso σS-Miyako follows line C to Hydrogen 14i Ironworks Direction 2
', and the remainder is recycled and used in the coal liquefaction step 34', where hydrogen for coal liquefaction is mixed with gas for preparing hydrogen-enriched U.

(図示せず)。液化油は’at製品として糸外に払い出
されるが、一部は石炭液化用済剤として循環使用される
ことも出来る。また、浴剤精製炭の全量またはその一部
はラインfを通ってコークス炉1′に送られ、コークス
炉装入炭中に配合されてコークス化ちれる。コークスg
31′で製造畑れ1こ冶金用コークスはラインeを)j
lfi/)て取り出される◎史に、本発明の石炭液化工
程を第2図に基ついて詳細に説明する。
(not shown). The liquefied oil is discharged out of the line as an 'at product, but a portion can also be recycled as a coal liquefaction agent. Further, the entire amount or a portion of the bath agent refined coal is sent to the coke oven 1' through the line f, and is blended into the coal charged in the coke oven to be coked. coke g
31' is the manufacturing field for metallurgical coke (line e))
The coal liquefaction process of the present invention will be explained in detail with reference to FIG. 2.

あらかじめ過当な粒度に粉砕・乾燥された石炭類と石炭
液化用済剤は混合Ilで混合し、スラリー化される。こ
の時の石炭液化用浴剤は全量粗タールを使用することか
好しいが本工程の蒸貿装随11から(ロ)収される循環
酷刑を含む徂タールを用いても差支えない。循環61剤
σ)混合量が50wt%以上になると製品である爵剤製
精炭および液化油σ)収率が低下する0筐た。必要があ
れは妖系化合物寺からなる触媒をスラIJ Igに飽加
しても良い。石炭の処理量を増大するには石炭類/浴剤
の軍址比が大きい万が有利であるが、同時にスラリー粘
度−65上昇してポンプの負荷が増大する。したがって
Coal that has been previously crushed and dried to an appropriate particle size and coal liquefaction agent are mixed in a mixing Il to form a slurry. At this time, it is preferable to use the entire amount of crude tar as the bath agent for coal liquefaction, but it is also possible to use the tar containing cyclic torture collected from the vaporization equipment 11 of this process. When the circulating 61 agent σ) mixture amount exceeds 50 wt%, the yield of the products, ie refined coal and liquefied oil σ), decreases. If necessary, you can saturate Sura IJ Ig with a catalyst consisting of a monster compound temple. In order to increase the throughput of coal, it is advantageous to have a large ratio of coal/bath agent, but at the same time, the viscosity of the slurry increases by -65%, increasing the load on the pump. therefore.

石炭類/浴剤の重量比は110.5〜l/4が好ましい
The weight ratio of coal/bath agent is preferably 110.5 to 1/4.

また、混合積lでのスラリー粘度を下げる1こめに。Also, to reduce the slurry viscosity in the mixing volume 1.

あらかじめ浴剤な80〜150’cに加温して供給して
もよいし、1だ、混合惜を80〜150℃に加温しても
さしつかえない。
The bath salt may be heated to 80 to 150 degrees Celsius before supplying it, or the mixture may be heated to 80 to 150 degrees Celsius.

以上により調整されたスラリーはスラリーフィードポン
プ2で70城/ cnI 拳G以上、好ましくは100
〜150kg/ca11Gに加圧された埃、あらかじめ
同じ圧力に加圧烙れた水素濃度70VO1%以上のカス
と混合きれる。カス中の水素濃度か70VOI係未滴で
は石炭類の液化時に反応器内の水素分圧が低下し、コー
キング等のトラブルを生じるため好1しくない。水素襄
Ij!i 7 ovo 1%以上のカスケ得るには水素
濃度80VOlチ以上の石炭液化用水素に敵性カス除去
装置6から送られる排カスの一部欠混合し調整すること
が出来る。これにより、水素精製装置Mに送る排カス財
乞制御し、水素和製装置の負荷を軽減することができる
。ついでスラIJ−は加熱炉3に導入され、温度30−
0〜500℃、好ましくは350〜470℃の範囲に加
熱され1反応器4に導びかれる。反応器での滞留時間は
最尚120分間、好1しくは10〜60分間である。以
上の処理により石炭中の七伎物質を十分に石剤中に陪解
さゼた後、気τ佼分醐器5によりカス状生成物を分離す
る。分離したカス状生成物は敵性ガス除去装置6に送ら
れ、硫化水素、炭酸カス等の敵性ガスを除去し、水素画
度を尚めた後、一部は石炭数比用水素製造θ)ために水
素和製装置(第1図2′)に送られ、残りは水素磁度調
製のために石炭液化用浴剤と混合されsP+び反応に洪
される。−万、カス状物質を分離した未浴解石炭、灰、
触媒およびmm石炭からなる石炭浴液は減圧弁7を通し
て減圧きれた後、場合によってはU過器、遠心分離。
The slurry adjusted as above is 70 jo/cnI fist G or more with slurry feed pump 2, preferably 100
Dust pressurized to ~150kg/ca11G can be completely mixed with scum with a hydrogen concentration of 70VO1% or more that has been previously pressurized and heated to the same pressure. If the hydrogen concentration in the waste is less than 70 VOI, the partial pressure of hydrogen in the reactor will decrease during liquefaction of coal, which will cause troubles such as coking, which is not preferable. Hydrogen Ij! i 7 ovo In order to obtain a slag of 1% or more, the waste slag sent from the hostile scum removing device 6 can be partially mixed with hydrogen for coal liquefaction having a hydrogen concentration of 80 VOl or more. Thereby, it is possible to control the amount of waste gas sent to the hydrogen purification device M and reduce the load on the hydrogen purification device. Then, the slurry IJ- is introduced into the heating furnace 3 and the temperature is 30-
It is heated to a temperature in the range of 0 to 500°C, preferably 350 to 470°C, and introduced into one reactor 4. The residence time in the reactor is at most 120 minutes, preferably 10 to 60 minutes. After the Shichiki substance in the coal is sufficiently dissolved in the stone agent through the above-described treatment, the dregs-like product is separated by the ki τ 佼 pulverizer 5. The separated scum-like product is sent to the hostile gas removal device 6, where hostile gases such as hydrogen sulfide and carbonic acid scum are removed and the hydrogen concentration is improved. Then, it is sent to a hydrogenation equipment (Fig. 1, 2'), and the remainder is mixed with a bath agent for coal liquefaction to prepare hydrogen magnetism and subjected to an sP+ reaction. −10,000, unbathed coal from which dregs have been separated, ash,
After the coal bath liquid consisting of the catalyst and mm coal is depressurized through the pressure reducing valve 7, it is subjected to U-filter and centrifugal separation depending on the case.

液体サイクロンまたは溶剤抽出法等の固敢分離装[同8
に導入り、未浴解石炭、灰および触媒等からなる4浴性
物質を分M1:する。ついで、4浴性物質を分離した石
炭浴液あるいは葦た不浴性物質乞分離しない石炭浴液は
加熱炉9を通して蒸発器]0゛に導入され、液体生成物
と釜残である浴剤精製炭とを回収する。尚、ここで得ら
れる溶剤lVJ製炭中σ)灰分は少ない方が好筐しいが
、li!Ll液分離装置ασ)設備費、運転費の増大お
よび液体生成物と沼剤布製炭σ)回収率低下等をまねく
ため、冶金用コークス製造時に影替を与えない和も即ち
、溶剤精製炭中の灰分が10wt%以下、好筐しくは4
wt%以下になるように4浴性物質を分離するのが良い
。葦た。蒸発器10より191収きれた成体生成物は製
品前として払い出される。あるいは蒸留装置11で精製
しvi環I剤の一部として使用することも出来る。
Solid separation equipment such as liquid cyclone or solvent extraction method [8
A four-bath substance consisting of unbathed cracked coal, ash, catalyst, etc. is separated into M1. Next, the coal bath liquid from which the four-bath substances have been separated or the coal bath liquid from which the non-bath substances have not been separated is introduced into the evaporator through the heating furnace 9, and the liquid product and the residue from the bath are purified. Collect charcoal. Incidentally, it is better to have a lower ash content in the solvent lVJ coal-making σ) obtained here, but li! Ll liquid separator ασ) Increase in equipment costs and operating costs, and decrease in recovery rate of liquid products and charcoal made from slag agent ασ). The ash content is 10wt% or less, preferably 4
It is preferable to separate the four-bath substances so that the amount is less than wt%. Reed. The 191 pieces of mature product collected from the evaporator 10 are discharged as a pre-product. Alternatively, it can be purified in the distillation apparatus 11 and used as part of the vi ring I agent.

−万、倚られた浴剤精製炭の全鼠葦たはそり)一部は同
化装置によって固化されるかあるいはまた固化せずに取
状のitコータス炉に装入する石炭に対して3〜12w
t% になるように配合されコークス化される。
- 1,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,000,0000,000,0000,0 12w
t% and coked.

以上1本発明において注目丁べき点は石炭液化用浴剤を
コークス炉から得られる粗タールで葦かなうことによっ
て従来から必セとしてさたイノn環浴剤の8緘性がほと
んどなく、シタがって石炭を尚Kに水素化分解して多撤
の油を得る必要もなく得られる油はその大部分を製品と
することができる。
As mentioned above, the noteworthy point in the present invention is that by replacing the bath agent for coal liquefaction with coarse tar obtained from a coke oven, there is almost no 8-thickness of the ino-ring bath agent, which has been a necessity in the past. Therefore, it is not necessary to hydrocrack coal to K to obtain a large amount of oil, and most of the obtained oil can be used as a product.

即ち、従来の石炭?&化法に比べてより欅やかな反工6
条件でかつ簡便に操作しうる。また、粗タールと石炭類
の混合スラリーを水砥する1こめに最終製品として得ら
れる浴剤精製炭はいわゆる通常の石炭液化物である浴剤
精製炭と粗タール中のコールタールピッチの水素化物と
の混合物となり、従来の石炭液化法に比べるとその収率
が著しく多いはかりでな(、冶金用コークス製造用ω≦
加剤あるいはニードルコークス、炭素繊維寺の炭素材原
料としても良好である。筐1こ、液化油も比教的軽實で
ありBTX等の化学原料を多、嵐に回収することか可曲
であるとともに、ティーゼルエンジン等の燃料油として
使用することもnJ北である。
i.e. conventional coal? & Anti-technical method 6, which is more attractive than the chemical method
It can be easily operated under certain conditions. In addition, the bath agent refined coal obtained as the final product after grinding the mixed slurry of crude tar and coal with water is a mixture of the bath agent refined coal, which is a so-called ordinary coal liquefied product, and the hydride of coal tar pitch in the crude tar. The yield is significantly higher than that of the conventional coal liquefaction method (for metallurgical coke production ω≦
It is also good as an additive, needle coke, and carbon material raw material for carbon fiber temples. Liquefied oil is also a religious light product, and it is flexible enough to be used to collect chemical raw materials such as BTX, and it is also useful to use it as fuel oil for teasel engines.

また、コークス炉ガスと本発明の石炭液化工程から回収
される排カスとの混合カスを水素和製装置(第1図2′
)で精製することによって1石炭液化工程(第1図3′
〕で必要とする石炭欣化用水素は第1凶ラインby、−
通り十分に補なうことができる。同時に、混合ガスの精
製時に副生するガスは炭化水漏カスを多量に含む茜カロ
リーカスであり第1凶ラインb′を通りコークス炉用燃
料はル・りでなく石炭液化用燃料σ)一部として使用出
来る。特に、鞘蛋なコントロールン必要とする加熱炉ハ
J燃料として使用でき1石炭欧化工程(第1図3′)の
運転操作を1)1」便にするとともに燃料費の動減を+
tiることかできる。
In addition, the mixed scum of coke oven gas and waste sludge recovered from the coal liquefaction process of the present invention was used in a hydrogenation equipment (Fig. 1, 2').
1 coal liquefaction process (Fig. 1 3'
] The hydrogen required for coal conversion is the first line by -
can be fully compensated for. At the same time, the gas that is produced as a by-product during the refining of the mixed gas is red caloric waste that contains a large amount of hydrocarbon residue, and it passes through the first line b' and becomes the fuel for coke ovens, not the coal liquefaction fuel σ)1. It can be used as a part. In particular, heating furnaces that require extensive control can be used as J fuel, making the operation of the 1 coal Europeanization process (Fig. 1 3') easier and reducing fluctuations in fuel costs.
I can say ti.

更に1本発明の痔剤鞘製炭を旧館用コータス製造用除加
ハリとして使用すると、コークス炉に装入する配合灰中
の強粘結炭の一部ン全く粘結性のない非粘結炭と直侠す
ることが出来1強粘結炭の供給が困難な地域にとって非
宮に市川となる。しかも1本発明の石炭欣化工程−コー
クス装這工杜結合プロセスを製鉄所と隣接し10地域に
建設ずれは。
In addition, when the hemorrhoid sheath charcoal of the present invention is used as a removing stiffener for producing coatas for old buildings, a portion of the highly caking coal in the blended ash charged into a coke oven becomes non-caking, with no caking at all. It can be used directly with charcoal, making it ideal for areas where it is difficult to supply strong coking coal. Moreover, the construction of the present invention's coal filtration process and coke coating process in 10 areas adjacent to the steelworks.

本発明の方法で得られる78金用コークスを直接製鉄所
に供給することかでき、より紅硲的な石炭液化プロセス
となる。
The 78-karat gold coke obtained by the method of the present invention can be directly supplied to a steel mill, resulting in a more convenient coal liquefaction process.

以下、央す揚物をあけて本発明を更に具体的にωd明す
るが、これにより本発明は限足されるものではない。
Hereinafter, the present invention will be explained in more detail with reference to fried foods, but the present invention is not limited thereby.

実施例1 撹拌装置のつい1こ0.57万一トクレーブレζ日本顔
瀝青炭50v(無水無灰ベース)とコークス炉より回収
され1こ祖タール1501を入れ水系初圧120 kg
/cnlG ノ加圧下、3℃/ m I nの昇温運度
で450℃葦で昇温し、この温度で撹拌しなから60分
間保持して曲短十し1こ。そ”k* オートクレーブC
液とに分離し1こ。r畝はさらに10皿nHrσ)減圧
下350℃のカットポイントに至る豆で諷圧黒関し液状
生成vIJを回収し、さらに釜残として常温固体の俗剤
精製炭馨得1こ。結果を第1衣に示す。
Example 1 One of the stirrers was charged with 50v of Nippon Kao bituminous coal (anhydrous and ashless base) and 1501 tar recovered from a coke oven, and the initial pressure of the water system was 120 kg.
The temperature was raised to 450°C with a reed at a heating rate of 3°C/min under a pressure of 3°C/cnlG, and held at this temperature for 60 minutes without stirring. So”k* Autoclave C
Separate into liquid and 1 piece. Further, 10 plates (nHrσ) of the beans that reached the cut point of 350°C under reduced pressure were used to collect the liquid product vIJ, which was solid at room temperature, as the residue from the pot. The results are shown in Figure 1.

比較例1 撹拌v= wのつい1こ0.5tオートクレーブに実施
例1で使用と同様(1)日本産a肯炭502(無水無灰
ベース)とあらかじめこの日本産薗肯炭を水添して製造
し1こ循環浴剤1502馨入れて水製初圧120鴎/d
・G の加圧下、3℃/ m l nの昇温速匿で45
0℃”まで昇温し、この温度で撹拌りながら60分間保
持して俗解L1こ。その俵、実施例1と同様に処理して
カス、液状生成物および浴剤鞘製炭を伶だ。結果を第1
表に示す。
Comparative Example 1 A 0.5 t autoclave with stirring v=w was used in the same manner as used in Example 1. 1 bottle of circulating bath agent 1,502 liters is produced and the initial pressure of the water is 120/d.
・45 at a heating rate of 3℃/mln under pressure of G
The bales were heated to 0° C. and held at this temperature for 60 minutes with stirring. The bales were treated in the same manner as in Example 1 to remove the dregs, liquid product, and bath powder sheath charcoal. Results first
Shown in the table.

第1衣から1石炭の俗解率は実施で”11と比較例1と
もはeま同じ埴であるが、液体製品の社は本発明の方法
による芙11!I例1の万が浴Aリン俤塚する必要がな
い1こめ者しく多い。また、浴剤iFf’f製炭v)、
i8′!。
The common understanding rate of 1 coal from 1st coating is ``11'' and comparative example 1 are the same clay, but the liquid product company is using the method of the present invention. There are many cases where there is no need to wash the bath salts.
i8′! .

も柑タール中の水飴きれ1こピッチが言1れるため多い
It is also common because one pitch of starch syrup in citrus tar is said to be one pitch.

カスの兜生加、は実施Vlllの力が明らかに多く。Kabutouka of Kasu clearly has a lot of power in implementation.

特にメタン、エタン等が多く党生するため、ガスの黒鍵
が旨く、コークス炉及び石炭数比工程のn源として十分
1使用することができる。
In particular, since a large amount of methane, ethane, etc. are produced, the gas black key is effective and can be used as a source for coke ovens and coal ratio processes.

このように本発明の方法による石炭族化工桟−コークス
装道工程結合プロセスは、液体及び固体製品の収率が渚
しく而<、Lかも市カロリーカスが多量[発生するため
、従来法に比べて者しく紅済的な方法である。
As described above, the combined coal-coke processing process according to the method of the present invention has low yields of liquid and solid products, and generates a large amount of caloric gas compared to the conventional method. This is a very clever and Hongji method.

比較例2 欠施例1で使用したと同様のオートクレーブに日本産g
、f炭s o y (孟水無灰ベース)と浴剤としてコ
ークス炉より回収芒れた粗タール751とあらかじめこ
の日本pr説竹炭を水添して製造した循環浴剤751を
入れスラリー化した後夾施例1と同様にして俗解し1こ
。その結果を第1衣ば示す。
Comparative Example 2 Japanese g was placed in the same autoclave as used in Example 1.
, f charcoal soy (ashless base), crude tar 751 recovered from a coke oven as a bath agent, and circulation bath agent 751, which was previously produced by hydrogenating this Japanese PR theory bamboo charcoal, were added to form a slurry. Similar to Example 1, this is a common interpretation. The results will be shown in the first section.

実施例2 実施例1と同体にして象州芹亜U:官炭ン浴騨した。結
果を第1表に示す。
Example 2 The same product as Example 1 was prepared in Xiangzhou Seriya U: Government Charcoal Bath. The results are shown in Table 1.

実施例3 実施向lで使用しfこと同様のオートクレーブに毅州韮
褐炭50?(無水無灰ベース)とコークス炉より回収で
・れ1こ祖タール150yおよび111!に媒を0.7
5f’入れスラリー化り実施例1と同体にして俗解した
。A力来を第1表に小丁。
Example 3 In the same autoclave used in the practical direction, 50% of Yishu Niraguri brown coal was placed in a similar autoclave. (Anhydrous and ashless base) and recovered from coke ovens.Re1 original tar 150y and 111! medium to 0.7
5f' was added to form a slurry and was commonly understood as the same as Example 1. A Riki is listed in the first table.

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

第1図は本発明の一実施態祿を示すフローシートであり
、第2図は本発明の液化工程の一実施態様を示すフロー
シートである。 図中1′・・・コークス炉、2′・・・水素精製装置、
3′・・・石炭液化装置、a・・・コークス炉カスライ
ン、b・・・水素ライン、b′・・・削性カスライン、
C・・・石炭液化工程排カスラ1ン、d・・・粗タール
ライン、e・・・コークスライン、l・・・混合偲、2
・・・スラリーフィードポンプ。 3・・・加熱炉、4・・・反応器、5・・・気液分離器
、6・・・ば性ガス除去装歯2.7・・・減圧弁、8・
・・li!J液分離装置。
FIG. 1 is a flow sheet showing one embodiment of the present invention, and FIG. 2 is a flow sheet showing one embodiment of the liquefaction process of the present invention. In the figure, 1'...Coke oven, 2'...Hydrogen purification equipment,
3'... Coal liquefaction equipment, a... Coke oven waste line, b... Hydrogen line, b'... Cutting waste line,
C... Coal liquefaction process waste slurry 1 line, d... Crude tar line, e... Coke line, l... Mixing line, 2
...Slurry feed pump. 3... Heating furnace, 4... Reactor, 5... Gas-liquid separator, 6... Rubber gas removal gear 2.7... Pressure reducing valve, 8...
...li! J liquid separation device.

Claims (1)

【特許請求の範囲】 1、 コークス製造工程で得られる粗タールを石炭液化
用浴剤として石炭液化工程で使用するとともに、コーク
ス炉ガスと石炭液化工程からの排カスとの混合ガスを精
製し石炭液化用水素として石炭液化工程で使用り1石炭
液化工程で得られる浴剤精製炭の全量または一部をコー
クス炉装入炭中に配合使用することを特徴とする石炭液
化工程−コークス製造工程結合プロセス。 2、該石炭液化用水素の全量を該コークス製造工程で得
られる粗タールでまかなうことを特徴とする特許請求の
範囲第1項記載の結合プロセス。 3、該石炭液化用水素中の水素ぴ度が70VOlチ以上
であることを特徴とする特許請求σ)範囲第1項または
第2項記載の結合プロセス。
[Claims] 1. The crude tar obtained in the coke manufacturing process is used as a bath agent for coal liquefaction in the coal liquefaction process, and the mixed gas of coke oven gas and waste residue from the coal liquefaction process is purified to produce coal. Coal liquefaction process-coke production process combination characterized in that all or part of the bath agent refined coal obtained in the coal liquefaction process is used as hydrogen for liquefaction in the coke oven charging coal. process. 2. The combining process according to claim 1, characterized in that the entire amount of hydrogen for the coal liquefaction is provided by crude tar obtained in the coke manufacturing process. 3. The bonding process according to claim 1 or 2, characterized in that the hydrogen purity in the hydrogen for coal liquefaction is 70 VOl or more.
JP2576384A 1984-02-14 1984-02-14 Connected process of coal liquefaction process and coke preparation process Pending JPS60170693A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2576384A JPS60170693A (en) 1984-02-14 1984-02-14 Connected process of coal liquefaction process and coke preparation process
IN286/CAL/84A IN160158B (en) 1984-02-14 1984-04-30

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2576384A JPS60170693A (en) 1984-02-14 1984-02-14 Connected process of coal liquefaction process and coke preparation process

Publications (1)

Publication Number Publication Date
JPS60170693A true JPS60170693A (en) 1985-09-04

Family

ID=12174871

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2576384A Pending JPS60170693A (en) 1984-02-14 1984-02-14 Connected process of coal liquefaction process and coke preparation process

Country Status (2)

Country Link
JP (1) JPS60170693A (en)
IN (1) IN160158B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03243691A (en) * 1990-02-20 1991-10-30 Agency Of Ind Science & Technol Coliquefaction of coal with bituminous material using acid-type iron oxide catalyst
CN112032559A (en) * 2020-07-23 2020-12-04 中国神华煤制油化工有限公司 Coal liquefaction system, pipe network assembly thereof and start-up method

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52132001A (en) * 1976-04-30 1977-11-05 Nippon Kokan Kk <Nkk> Reformation of coal
JPS52134601A (en) * 1976-05-06 1977-11-11 Mitsui Cokes Kogyo Kk Method of producing upgraded coal
JPS5321682A (en) * 1976-08-11 1978-02-28 Yoshinao Katano Liquid tripping cap
JPS5444002A (en) * 1977-09-16 1979-04-07 Nippon Musical Instruments Mfg Regenerated plywood and laminated rectangular timber using same

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52132001A (en) * 1976-04-30 1977-11-05 Nippon Kokan Kk <Nkk> Reformation of coal
JPS52134601A (en) * 1976-05-06 1977-11-11 Mitsui Cokes Kogyo Kk Method of producing upgraded coal
JPS5321682A (en) * 1976-08-11 1978-02-28 Yoshinao Katano Liquid tripping cap
JPS5444002A (en) * 1977-09-16 1979-04-07 Nippon Musical Instruments Mfg Regenerated plywood and laminated rectangular timber using same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03243691A (en) * 1990-02-20 1991-10-30 Agency Of Ind Science & Technol Coliquefaction of coal with bituminous material using acid-type iron oxide catalyst
CN112032559A (en) * 2020-07-23 2020-12-04 中国神华煤制油化工有限公司 Coal liquefaction system, pipe network assembly thereof and start-up method

Also Published As

Publication number Publication date
IN160158B (en) 1987-06-27

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