JPH0735882B2 - Pulverized coal combustion method - Google Patents

Pulverized coal combustion method

Info

Publication number
JPH0735882B2
JPH0735882B2 JP60256350A JP25635085A JPH0735882B2 JP H0735882 B2 JPH0735882 B2 JP H0735882B2 JP 60256350 A JP60256350 A JP 60256350A JP 25635085 A JP25635085 A JP 25635085A JP H0735882 B2 JPH0735882 B2 JP H0735882B2
Authority
JP
Japan
Prior art keywords
pulverized coal
combustion
temperature
flame
burner
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 - Fee Related
Application number
JP60256350A
Other languages
Japanese (ja)
Other versions
JPS62116813A (en
Inventor
俊雄 諏訪
伸明 小林
堯 平野
Original Assignee
日本酸素株式会社
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 日本酸素株式会社 filed Critical 日本酸素株式会社
Priority to JP60256350A priority Critical patent/JPH0735882B2/en
Priority to US07/086,146 priority patent/US4744315A/en
Priority to DE19863690575 priority patent/DE3690575T1/de
Priority to PCT/JP1986/000581 priority patent/WO1987003066A1/en
Priority to DE3690575A priority patent/DE3690575C2/en
Publication of JPS62116813A publication Critical patent/JPS62116813A/en
Publication of JPH0735882B2 publication Critical patent/JPH0735882B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は微粉炭燃焼方法に係り、特にスチールスクラッ
プ溶解用電気炉、アルミニウム,銅等の溶解炉用バーナ
における微粉炭燃焼方法に関するものである。
The present invention relates to a pulverized coal combustion method, and more particularly to a pulverized coal combustion method in an electric furnace for melting steel scrap and a burner for a melting furnace for melting aluminum, copper or the like. .

〔従来の技術〕[Conventional technology]

スチールスクラップ,アルミニウム,銅等の溶解用バー
ナにあっては、大部分は重油等の液体燃料と酸素,酸素
富化空気あるいは空気を使用しており、一部は特開昭59
−115904号公報にみられるように微粉炭と気体燃料の混
焼、もしくは微粉炭と液体燃料の混焼としている。
Most of the burners for melting steel scrap, aluminum, copper, etc. use liquid fuel such as heavy oil and oxygen, oxygen-enriched air or air, and some of them are disclosed in JP-A-59-59.
As disclosed in Japanese Patent Laid-Open No. 115904, co-firing of pulverized coal and gaseous fuel or co-firing of pulverized coal and liquid fuel.

ところで、エネルギーコストの安い微粉炭の燃焼速度は
重油等の液体燃料に比して非常に遅く、スチールスクラ
ッ等の溶解能力がほとんどないため、エネルギーコスト
の高い重油等の液体燃料の使用が大半を占めている。
By the way, the combustion speed of pulverized coal with low energy cost is much slower than that of liquid fuels such as heavy oil, and it has almost no dissolution capacity such as steel scrap, so most of liquid fuels such as heavy oil with high energy cost are used. is occupying.

そして、微粉炭と液体燃焼あるいは微粉炭と気体燃料と
の混焼による場合、スチールスクラップ,アルミニウ
ム,銅等の冷材供給時は、バーナ近傍では炉壁からの輻
射熱が少なく、微粉炭のみでは安定なる火炎が得られ
ず、また消炎することもあるため、バーナ近傍の温度が
高くなるまでは液体燃料や気体燃料の混入割合を多く
し、バーナ近傍の温度が高くなってからこの混入割合を
少なくしている。
When pulverized coal and liquid combustion or mixed combustion of pulverized coal and gas fuel are used, when radiating heat such as steel scrap, aluminum, and copper, radiant heat from the furnace wall is small near the burner, and only pulverized coal is stable. Since a flame may not be obtained and may extinguish, increase the mixing ratio of liquid fuel or gaseous fuel until the temperature near the burner rises, and decrease this mixing ratio after the temperature near the burner rises. ing.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

しかしながら、この微粉炭と液体燃料や気体燃料の混焼
は、重油等の燃焼に比してエネルギーコストは安くなる
ものの、微粉炭専焼と比較した場合にはやはりエネルギ
ーコストは高くなり、かつ微粉炭の混焼バーナは構造が
複雑となる欠点があった。
However, although the energy cost of this pulverized coal and liquid fuel or gas fuel co-firing is lower than that of combustion of heavy oil, the energy cost is also high when compared with pulverized coal exclusive combustion, and The co-firing burner has a drawback that the structure is complicated.

そこで、本発明は、スクラップ溶解用電気炉,アルミニ
ウム,銅等の金属の溶解炉用バーナにおいて、特に炉内
バーナ近傍が微粉炭着火に不充分な温度でも、高温(20
00℃以上)でかつ安定した火炎を形成し、充分なる溶解
能力を有する微粉炭専焼が可能な微粉炭燃焼方法を提供
することを目的とする。
Therefore, the present invention provides a scrap melting electric furnace, a burner for melting a metal such as aluminum or copper, and a high temperature (20%) even when the temperature in the vicinity of the burner is insufficient for ignition of pulverized coal.
It is an object of the present invention to provide a pulverized coal combustion method capable of forming a stable flame at a temperature of at least 00 ° C.) and having a sufficient melting ability and capable of pulverized coal combustion alone.

〔問題点を解決するための手段〕[Means for solving problems]

上記目的を達成するため、本発明方法は、80℃以上に予
熱した酸素濃度30%以上の支燃性ガスと300℃以下に予
熱した微粉炭とを燃焼させて微粉炭燃焼火炎を形成し、
該火炎でスチールスクラップ,アルミニウム,銅等の金
属を溶融するにあたり、T=支燃性ガス温度〔℃〕,C=
支燃性ガス中の酸素濃度〔%〕,t=微粉炭温度〔℃〕と
すると、 T≧exp{14.14−1.84・InC−exp(0.01127t−3.44
4)}の条件を満たすように燃焼せしめることを特徴と
するものである。
In order to achieve the above object, the method of the present invention forms a pulverized coal combustion flame by burning a combustion-supporting gas having an oxygen concentration of 30% or more preheated to 80 ° C. or more and pulverized coal preheated to 300 ° C. or less,
When melting metal such as steel scrap, aluminum, and copper with the flame, T = flammable gas temperature [° C], C =
Assuming that the oxygen concentration in the combustion-supporting gas [%], t = pulverized coal temperature [° C], T ≥ exp {14.14-1.84 ・ InC-exp (0.01127t-3.44)
4)} is characterized in that it is burned so as to satisfy the condition.

スチールスクラップ,アルミニウム,銅等の金属の溶解
バーナとしては、重油等の液体燃料の燃焼特性に近い火
炎の形成が要求される。火炎温度としては約2000℃以上
必要となる。またバーナ近傍の雰囲気温度が数百度程度
でも安定かつ高温なる火炎の形成が要求される。
As a melting burner for metals such as steel scrap, aluminum and copper, it is required to form a flame close to the combustion characteristics of liquid fuel such as heavy oil. The flame temperature must be about 2000 ° C or higher. Further, it is required to form a flame that is stable and high even if the ambient temperature near the burner is about several hundred degrees.

ところで、揮発成分約15〜30%,固定炭素45〜60%なる
微粉炭を大気雰囲気中で常温20℃酸素にて燃焼したが火
炎を形成することができなかった。そこで、酸素温度15
0℃,微粉炭温度150℃に予熱したところ、約2000℃の安
定した火炎を得ることができ、支燃性ガス中の酸素濃
度,支燃性ガス予熱温度,微粉炭予熱温度の関係におい
て安定なる火炎形成ゾーンは第1図に示す関係、即ちT
≧exp{14.14−1.84・InC−exp(0.01127t−3.444)}
の関係であることを見出した。
By the way, pulverized coal consisting of about 15 to 30% of volatile components and 45 to 60% of fixed carbon was burned at a normal temperature of 20 ° C. oxygen in an air atmosphere, but a flame could not be formed. Therefore, the oxygen temperature 15
When preheated to 0 ℃ and pulverized coal temperature of 150 ℃, a stable flame of about 2000 ℃ can be obtained and stable in relation to oxygen concentration in combustion-supporting gas, combustion-gas preheating temperature, and pulverized coal preheating temperature. The flame forming zone is as shown in FIG.
≧ exp {14.14-1.84 ・ InC-exp (0.01127t-3.444)}
It was found that there is a relationship.

即ち、微粉炭はその予熱を300℃以上にすると低温ター
ルが抽出され微粉炭の搬送が困難となり、微粉炭の予熱
は最高300℃、支燃性ガス中の酸素濃度は30℃以上、支
燃性ガス予熱温度は80℃以上の範囲で微粉炭専焼バーナ
を用いて燃焼を行なうと約2000℃以上の火炎が形成でき
ることがわかった。本発明方法はかかる実情に基づき完
成させるに至った。
That is, if the preheat of pulverized coal is higher than 300 ° C, low temperature tar is extracted and it becomes difficult to convey the pulverized coal.The preheating of pulverized coal is up to 300 ° C, the oxygen concentration in the combustion supporting gas is 30 ° C or higher, It was found that a flame of about 2000 ° C or higher can be formed when combustion is performed using a pulverized coal burner with a preheating temperature of the characteristic gas of 80 ° C or higher. The method of the present invention has been completed based on this situation.

〔実施例〕〔Example〕

以下、本発明方法の実施例を示す。 Examples of the method of the present invention will be shown below.

微粉炭(揮発成分15〜30%,固定炭素45〜60%,灰分10
〜20%,粒度200メッシュ以下85%)を260℃に予熱し、
支燃性ガス中の酸素濃度を30〜100%,支燃性ガス温度
を700℃にして、バーナにて微粉炭を大気中で燃焼し、
安定なる火炎を得、その火炎温度を測定した。
Pulverized coal (volatile components 15-30%, fixed carbon 45-60%, ash 10
~ 20%, particle size 200 mesh or less 85%) is preheated to 260 ℃,
The oxygen concentration in the combustion-supporting gas is 30 to 100%, the temperature of the combustion-supporting gas is 700 ° C., and pulverized coal is burned in the atmosphere with a burner.
A stable flame was obtained and the flame temperature was measured.

その結果を第2図に示す。この第2図からもわかる通
り、火炎温度は2000〜2400℃と高温であり、スチールス
クラップ,アルミニウム,銅等の溶解能力も良かった。
The results are shown in FIG. As can be seen from FIG. 2, the flame temperature was as high as 2000 to 2400 ° C, and the ability to dissolve steel scrap, aluminum, copper, etc. was also good.

〔発明の効果〕〔The invention's effect〕

以上のように、酸素濃度30%以上含有する支燃性ガスを
80℃以上に予熱し、かつ微粉炭を最高300℃に予熱し
て、微粉炭を支燃性ガスと燃焼させるにあたり、本発明
方法はT≧exp{14.14−1.84・InC−exp(0.01127t−3.
444)}の条件を満たすように燃焼せしめるから、スチ
ールスクラップ,アルミニウム,銅等の金属の溶解にお
ける、高温なる火炎温度(約2000℃以上),溶解能力が
要求されるバーナにおいて、エネルギーコストの安い微
粉炭の専焼が可能になる。
As described above, the combustion-supporting gas containing 30% or more of oxygen concentration
In preheating to 80 ° C. or higher and preheating pulverized coal to a maximum of 300 ° C. and burning the pulverized coal with the combustion-supporting gas, the method of the present invention is T ≧ exp {14.14−1.84 · InC−exp (0.01127t− 3.
444)} is burned to satisfy the conditions of (444)}, so the energy cost is low in burners that require high flame temperatures (about 2000 ° C or higher) and melting capacity in melting metals such as steel scrap, aluminum, and copper. The pulverized coal can be burned exclusively.

また、微粉炭の専焼が可能なことで、微粉炭と液体燃料
あるいは気体燃料との混焼バーナに必要な混焼部及び液
体,気体燃料用の装置が不要となり、微粉炭と液体燃
料、微粉炭と気体燃料の混焼バーナに比べコンパクトな
バーナとすることができる。
In addition, since the pulverized coal can be burnt exclusively, the co-firing part and the liquid and gas fuel devices necessary for the co-firing burner of pulverized coal and liquid fuel or gas fuel are not required, and pulverized coal and liquid fuel or pulverized coal The burner can be made more compact than the mixed burner for gaseous fuel.

【図面の簡単な説明】[Brief description of drawings]

第1図は支燃性ガス中の酸素濃度,支燃性ガス予熱温度
及び微粉炭予熱温度と安定なる火炎形成ゾーンの関係を
示すグラフ図、第2図は微粉炭予熱温度260℃,支燃性
ガス予熱温度700℃にした場合の支燃性ガス中の酸素濃
度と火炎温度との関係を示すグラフ図である。
Fig. 1 is a graph showing the relationship between oxygen concentration in combustion-supporting gas, preheating temperature of combustion-supporting gas, pulverized coal preheating temperature, and stable flame formation zone. Fig. 2 is pulverized coal preheating temperature of 260 ℃, combustion-supporting zone. FIG. 6 is a graph showing the relationship between the oxygen concentration in the combustion-supporting gas and the flame temperature when the preheating temperature of the propellant gas is 700 ° C.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】80℃以上に予熱した酸素濃度30%以上の支
燃性ガスと300℃以下に予熱した微粉炭とを燃焼させて
微粉炭燃焼火炎を形成し、該火炎でスチールスクラッ
プ,アルミニウム,銅等の金属を溶融するにあたり、T
=支燃性ガス温度〔℃〕,C=支燃性ガス中の酸素濃度
〔%〕,t=微粉炭温度〔℃〕とすると、 T≧exp{14.14−1.84・InC−exp(0.01127t−3.44
4)}の条件を満たすように燃焼せしめることを特徴と
する微粉炭燃焼方法。
1. A pulverized coal combustion flame is formed by burning a combustion-supporting gas having an oxygen concentration of 30% or more preheated to 80 ° C. or more and pulverized coal preheated to 300 ° C. or less, and steel scrap or aluminum is produced by the flame. When melting metals such as copper, T
= Turn gas temperature [℃], C = Oxygen concentration in fuel gas [%], t = Pulverized coal temperature [℃], T ≧ exp {14.14-1.84 ・ InC-exp (0.01127t- 3.44
4)} Pulverized coal combustion method characterized by burning so as to satisfy the condition of.
JP60256350A 1985-11-15 1985-11-15 Pulverized coal combustion method Expired - Fee Related JPH0735882B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP60256350A JPH0735882B2 (en) 1985-11-15 1985-11-15 Pulverized coal combustion method
US07/086,146 US4744315A (en) 1985-11-15 1986-11-14 Process for burning pulverized coal
DE19863690575 DE3690575T1 (en) 1985-11-15 1986-11-14
PCT/JP1986/000581 WO1987003066A1 (en) 1985-11-15 1986-11-14 Method of combustion of finely divided coal
DE3690575A DE3690575C2 (en) 1985-11-15 1986-11-14 Pulverised coal combustion method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60256350A JPH0735882B2 (en) 1985-11-15 1985-11-15 Pulverized coal combustion method

Publications (2)

Publication Number Publication Date
JPS62116813A JPS62116813A (en) 1987-05-28
JPH0735882B2 true JPH0735882B2 (en) 1995-04-19

Family

ID=17291457

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60256350A Expired - Fee Related JPH0735882B2 (en) 1985-11-15 1985-11-15 Pulverized coal combustion method

Country Status (1)

Country Link
JP (1) JPH0735882B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0563828B1 (en) * 1992-03-27 1999-12-22 Nippon Sanso Corporation Method of melting metals

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56149214U (en) * 1980-04-09 1981-11-10
JPS5824712A (en) * 1981-08-06 1983-02-14 Kobe Steel Ltd Method of blow-in combustion of pulverized coal

Also Published As

Publication number Publication date
JPS62116813A (en) 1987-05-28

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