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JPH0323801B2 - - Google Patents
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JPH0323801B2 - - Google Patents

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Publication number
JPH0323801B2
JPH0323801B2 JP56033188A JP3318881A JPH0323801B2 JP H0323801 B2 JPH0323801 B2 JP H0323801B2 JP 56033188 A JP56033188 A JP 56033188A JP 3318881 A JP3318881 A JP 3318881A JP H0323801 B2 JPH0323801 B2 JP H0323801B2
Authority
JP
Japan
Prior art keywords
temperature
furnace
amount
air
approximately
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
Application number
JP56033188A
Other languages
Japanese (ja)
Other versions
JPS57148101A (en
Inventor
Kazuma Kikuoka
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.)
Mitsubishi Power Ltd
Original Assignee
Babcock Hitachi 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 Babcock Hitachi KK filed Critical Babcock Hitachi KK
Priority to JP3318881A priority Critical patent/JPS57148101A/en
Publication of JPS57148101A publication Critical patent/JPS57148101A/en
Publication of JPH0323801B2 publication Critical patent/JPH0323801B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】 この発明は回収ボイラの運転方法に係り、特に
薬品の回収率を高め、かつ硫黄酸化物等の大気汚
染物質の排出量を減少できる回収ボイラの運転方
法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method of operating a recovery boiler, and more particularly to a method of operating a recovery boiler that can increase the recovery rate of chemicals and reduce the amount of air pollutants such as sulfur oxides emitted.

パルプを製造する場合には、木材成分のセルロ
ーズ(繊維)とリグニン(樹脂)を分離してセル
ローズのみを取り出す必要があるが、この場合、
化学的分離を行うためNa2SやNaOH等の薬品を
用いる。蒸解や洗浄等のパルプ工程を経た溶解リ
グニンと上記薬品を含む溶液は黒液と称する廃液
として排出されるが、回収ボイラはこの黒液を燃
焼させて黒液中の無機薬品を還元してNa2Sや
Na2CO3を回収するとともに、パルププロセスお
よび他の機器に必要な蒸気を供給する。
When producing pulp, it is necessary to separate the wood components cellulose (fiber) and lignin (resin) and extract only the cellulose.
Chemicals such as Na 2 S and NaOH are used to perform chemical separation. The solution containing dissolved lignin and the above chemicals after pulping processes such as cooking and washing is discharged as a waste liquid called black liquor, but the recovery boiler burns this black liquor to reduce the inorganic chemicals in the black liquor and convert it into sodium. 2 Sya
It recovers Na 2 CO 3 and supplies the steam needed for the pulp process and other equipment.

回収ボイラの形式はスエーデン式とトムリンソ
ン式(アメリカ式)の二つに大別されるが、この
うちスエーデン式は黒液を細い粒子で炉内に噴霧
して炉内の放射熱により乾燥させ、微粉状の固形
物となつて炉底に落下堆積したものを燃焼させる
ものである。一方トムリンソン式は黒液を粗粒状
態で火炉壁面に向つて噴射し、これにより黒液は
燃焼ガス中を横切る間に一部脱水し、壁面に付着
した後火炉の放射熱により乾燥し、次々と炉底に
落下して堆積し燃焼させるものである。この二つ
の形式のうちスエーデン式は黒液の微粒子を浮遊
させて乾燥させるため燃焼ガス中に相当量の未燃
分(固形分)が含まれ、いわゆる未燃分のキヤリ
ーオーバーが生じこの結果未燃粒子がスラグスク
リーンや過熱器内で二次燃焼を起こし局部的高温
部が生じる。これに伴つて部分的に溶融したスメ
ルトが管群に固く付着してボイラの連続運転を妨
げることになる。またこの形式のボイラは燃焼温
度が比較的低いため排ガス中の大気汚染物質、特
に硫黄酸化物(SOx)の含有濃度が高くなり、か
つ薬品の還元率が低いという問題もある。
Recovery boilers are roughly divided into two types: the Swedish type and the Tomlinson type (American type). Of these, the Swedish type sprays black liquor in fine particles into the furnace and dries it using radiant heat inside the furnace. This is to burn the solid matter that falls to the bottom of the furnace in the form of fine powder. On the other hand, in the Tomlinson method, black liquor is injected in the form of coarse particles toward the furnace wall. As a result, the black liquor is partially dehydrated while passing through the combustion gas, and after adhering to the wall, it dries due to the radiant heat of the furnace. It falls to the bottom of the furnace, accumulates, and burns. Of these two types, the Swedish type suspends black liquor particles and dries them, so a considerable amount of unburned matter (solid matter) is included in the combustion gas, resulting in so-called carry over of unburned matter. Unburnt particles cause secondary combustion in the slag screen and superheater, creating localized high temperature areas. As a result, partially melted smelt adheres firmly to the tube group, interfering with continuous operation of the boiler. Additionally, this type of boiler has a relatively low combustion temperature, resulting in a high concentration of air pollutants, particularly sulfur oxides (SOx), in the exhaust gas, and a low rate of reduction of chemicals.

一方トムリンソン式のボイラにあつては、炉壁
面で黒液を乾燥させるため、前記の如く未燃粒子
のキヤリーオーバーは殆んど生ぜず、かつ黒液乾
燥の時間を十分とれるので黒液濃度のいかんを問
わず燃焼が良好である。また燃焼部における水分
が少ないので前記スエーデン式に比較して燃焼温
度が高く、この結果SOxの発生量を低く押えるこ
とができると共に薬品の還元率も高い。
On the other hand, in the Tomlinson type boiler, the black liquor is dried on the furnace wall surface, so there is almost no carryover of unburned particles as mentioned above, and there is sufficient time for the black liquor to dry, so the black liquor concentration It burns well regardless of the type of fuel. Furthermore, since there is less moisture in the combustion section, the combustion temperature is higher than that of the Swedish type, and as a result, the amount of SOx generated can be kept low and the reduction rate of chemicals is also high.

この発生の目的は上述したトムリンソン式回収
ボイラの利点を損うことなく、さらに高い還元率
を得、かつSOxの排出量をさらに低減できる回収
ボイラ運転方法を提供することにある。要するに
この発明は黒液を炉壁に粗粒状として吹き付け乾
燥しチヤーとして炉底に落下させチヤーベツトを
形成して燃焼させ薬品を回収する回収ボイラを運
転する方法において、炉底近傍に供給する一次空
気量を全空気供給量の約50%とし、二次空気量を
全空気量の約30%とし、チヤーベツトの温度を約
1000℃乃至1100℃とし、全空気供給量の約20%の
量の三次空気を供給し排ガス中の未燃成分を燃
焼、し二次空気による燃焼ガス温度を約1200℃乃
至1300℃にして運転する回収ボイラの運転方法で
あることを特徴とする。
The purpose of this generation is to provide a recovery boiler operating method that can obtain a higher reduction rate and further reduce SOx emissions without impairing the advantages of the Tomlinson type recovery boiler described above. In short, this invention is a method of operating a recovery boiler in which black liquor is sprayed in the form of coarse particles onto the furnace wall, dried, and dropped to the bottom of the furnace as a char to form a charvet, which is then combusted to recover chemicals. The amount of air supplied is approximately 50% of the total air supply amount, the secondary air amount is approximately 30% of the total air amount, and the temperature of the chartreuse is approximately 50% of the total air supply amount.
The temperature is 1000℃ to 1100℃, and tertiary air is supplied in an amount of about 20% of the total air supply to burn unburned components in the exhaust gas, and the combustion gas temperature due to secondary air is set to about 1200℃ to 1300℃. The method is characterized in that it is a method of operating a recovery boiler.

以下この発明の実施例を添付図面を参考に説明
する。
Embodiments of the present invention will be described below with reference to the accompanying drawings.

第1図はトムリンソン式の黒液燃焼ボイラを示
す。ボイラ本体1にはオツシレータ2が設けてあ
る。オツシレータ2は黒液Lを粗粒状で噴霧し、
噴霧された黒液は火炉を横断して対向する壁面に
付着して炉内の放射熱により乾燥される。壁面で
の乾燥の際に黒液内部には多数の気泡が生じ、乾
燥した多孔質の固形分(チヤー)は順次壁面より
剥れて炉底に落下してチヤーベツト3を形成す
る。チヤーベツト3を形成した固形分はこの炉底
において燃焼する。符号A1は一次空気を示し、
炉底近辺の前後壁および両側壁に形成した空気ノ
ズルより供給される。チヤーベツトの燃焼により
スメルトと称する溶融分が生じ、スメルトスパウ
ト4を経て炉外に排出されNa等有用な物質(薬
品)を回収する。一次空気A1はこれら有用物質
の還元反応に必要な熱量を確保するために供給す
るものであり、このためには少ない空気量で適正
な還元雰囲気を形成し、同時にチヤーベツト3の
温度を高く保持することが必要である。チヤーベ
ツト温度は後述するとおり、約1000℃以上、好ま
しくは約1050℃とすることが必要で、チヤーベツ
ト温度を以上の如く保持し、かつ還元雰囲気とす
るためには一次空気A1は全空気供給量の約50%
とする。火炉下部に形成した還元域を以上の温度
に保持することにより適量のナトリユーム塩が昇
華し、これが炉内ガス中に含まれるSOxと反応し
てナトリユーム化合物を形成する脱硫効果を発揮
する。次式(1)は脱硫の一例を示すものであつて、
SOx例えばSO2はNa2Oと反応してNa2SO4(亡硝)
を生ずる。
Figure 1 shows a Tomlinson type black liquor combustion boiler. The boiler main body 1 is provided with an oscillator 2. The oscillator 2 sprays black liquid L in coarse particles,
The sprayed black liquor crosses the furnace and adheres to the opposing wall surface, where it is dried by the radiant heat inside the furnace. During drying on the wall surface, a large number of air bubbles are generated inside the black liquor, and the dried porous solids (char) are successively peeled off from the wall surface and fall to the bottom of the furnace to form a charbet 3. The solids forming the chartreuse 3 are burned at the bottom of the furnace. The code A 1 indicates primary air,
Air is supplied from air nozzles formed on the front and rear walls and both side walls near the bottom of the furnace. A molten substance called smelt is produced by combustion of the chartreuse, which is discharged from the furnace through a smelt spout 4 to recover useful substances (chemicals) such as Na. Primary air A 1 is supplied to secure the amount of heat necessary for the reduction reaction of these useful substances, and for this purpose it is necessary to form an appropriate reducing atmosphere with a small amount of air and at the same time maintain the temperature of the chamber 3 at a high level. It is necessary to. As will be described later, the temperature of the chamber needs to be approximately 1000℃ or higher, preferably approximately 1050℃, and in order to maintain the temperature of the chamber as above and create a reducing atmosphere, the primary air A1 must be equal to the total air supply amount. Approximately 50% of
shall be. By maintaining the reduction zone formed at the bottom of the furnace at the above temperature, an appropriate amount of sodium salt sublimates, and this reacts with SOx contained in the furnace gas to produce a desulfurization effect to form sodium compounds. The following formula (1) shows an example of desulfurization,
SOx For example, SO 2 reacts with Na 2 O to form Na 2 SO 4 (dead nitrogen)
will occur.

Na2O+SO2+1/2O2→Na2SO4 ……(1) なお発生したNa2SO4はダストとしてボイラ出
口に配置した集塵器により捕集される。
Na 2 O + SO 2 + 1/2O 2 →Na 2 SO 4 ...(1) The generated Na 2 SO 4 is collected as dust by a dust collector placed at the boiler outlet.

第2図は発明者等が確認したチヤーベツト温度
とSO2の発生量の関係を示す。従来チヤーベツト
の温度は約700℃から約900℃の間であり、例えば
チヤーベツト温度が700℃〜800℃の間ではSO2
度が400〜600ppmであるのに対し、チヤーベツト
温度が約1000℃ではSO2濃度は100〜300ppmとな
り最高約1/6、平均して約1/3に低下することを確
認した。但し1100℃以上とすると窒素酸化物
(NOx)の生成量が増大するのでチヤーベツト温
度は前記のとおり1000〜1100℃、好適には1050℃
程度が良い。
FIG. 2 shows the relationship between the chartreuse temperature and the amount of SO 2 generated, as confirmed by the inventors. Conventionally, the temperature of a chartreuse is between about 700°C and about 900°C. For example, when the temperature of the chartreuse is between 700°C and 800°C, the SO 2 concentration is between 400 and 600 ppm, whereas when the temperature of the chartrette is about 1000°C, the SO 2 concentration is It was confirmed that the concentration of 2 was 100 to 300 ppm, with a maximum of about 1/6 and an average decrease of about 1/3. However, if the temperature is higher than 1100°C, the amount of nitrogen oxides (NOx) produced will increase, so the chamber temperature should be 1000 to 1100°C, preferably 1050°C, as mentioned above.
Good condition.

なお一次空気A1は以上の作用を営む外、後述
の二次空気A2と共にチヤーベツト3の形状を台
形に成形する作用の一部も営むものであつて、炉
底に落下した固形分をチヤーベツト上部に吹き上
げ、チヤーベツト全体を整形すると共に燃焼部で
あるチヤーベツト上部に新しい固形分を供給して
燃焼を良好に継続させる。
In addition to performing the above-mentioned functions, the primary air A 1 also performs a part of the function of shaping the chartreuse 3 into a trapezoidal shape together with the secondary air A2 described later, and it collects the solids that have fallen to the bottom of the furnace. The mixture is blown up to the top, shaping the entire chamber, and supplying new solids to the upper portion of the chamber, which is the combustion section, to ensure good continuation of combustion.

次にチヤーベツト3内部での還元作用を効果的
に行うためにはチヤーベツト3の表面温度を高
め、かつ温度分布が均一であることが好ましい。
このためにはチヤーベツト3の形状は第1図の如
く頂部が平坦な略台形に形成し、頂部全体が平均
して燃焼するよう構成する。つまり二次空気A2
の供給によりチヤーは主としてチヤーベツト3の
頂部で燃焼し、この燃焼の熱によりチヤーベツト
3内部に前記の如く約1000℃以上の高温の還元性
雰囲気を形成する。
Next, in order to effectively carry out the reducing action inside the chamber 3, it is preferable that the surface temperature of the chamber 3 is high and that the temperature distribution is uniform.
For this purpose, the shape of the chamber 3 is formed into a substantially trapezoidal shape with a flat top, as shown in FIG. 1, so that the entire top burns evenly. i.e. secondary air A 2
By supplying the char, the char burns mainly at the top of the charvet 3, and the heat of this combustion forms a high-temperature reducing atmosphere of about 1000° C. or higher inside the charvet 3 as described above.

第3図はこの発明に係る運転方法によるボイラ
各部の温度分布を示し、チヤーベツト3の温度
(符号Aで示す)は約1000℃〜1100℃となり、か
つチヤーベツト頂部に位置する二次空気ポート
(符号Bで示す)の温度は約1300℃〜1400℃とな
る。
FIG. 3 shows the temperature distribution of each part of the boiler according to the operating method according to the present invention. (denoted as B) is about 1300°C to 1400°C.

二次空気A2は二次空気ポート5から炉内に流
入し、黒液の乾燥および燃焼を完全に行わせるも
のであるが、150〜200mmAqの比較的高い風圧で
炉内噴射されるのでチヤーベツト3の頂部を平坦
にする作用も営むものである。チヤーベツト3を
以上の形状に形成することによりチヤーベツト温
度を1000℃以上の高温に保持ししかもチヤーベツ
ト内は燃焼用空気と隔離されているため高い還元
性雰囲気が形成でき薬品の還元効率を高めること
になる。二次空気A2はこのため前記風圧で、か
つ供給量は全空気供給量の約30%とするのが好ま
しい。
Secondary air A2 flows into the furnace from the secondary air port 5 and completely dries and burns the black liquor, but since it is injected into the furnace at a relatively high wind pressure of 150 to 200 mmAq, it is difficult to dry the black liquor. It also serves to flatten the top of 3. By forming the chamber 3 in the above shape, the temperature of the chamber can be maintained at a high temperature of 1000°C or more, and since the inside of the chamber is isolated from the combustion air, a highly reducing atmosphere can be formed, increasing the efficiency of reducing chemicals. Become. Therefore, it is preferable that the secondary air A 2 is at the above-mentioned wind pressure and the supply amount is about 30% of the total air supply amount.

A3は三次空気であつて、オツシレータ2の上
方から二次空気A2と同様の約150〜200mmAqの風
圧で供給され、炉内を強力に撹拌しながら炉底か
ら上昇する未燃分を完全に燃焼させる。なお三次
空気A3の供給量は全空気供給量の約20%であり、
かつ三次空気用エアポート(符号cで示す)の温
度は未燃分が再燃焼するため約1000〜1200℃程度
ある。
A 3 is tertiary air, and is supplied from above the oscillator 2 at a wind pressure of about 150 to 200 mmAq, similar to that of the secondary air A 2 , and completely removes unburned matter rising from the bottom of the furnace while strongly stirring the inside of the furnace. burn it. The supply amount of tertiary air A3 is approximately 20% of the total air supply amount,
In addition, the temperature of the tertiary air port (indicated by symbol c) is about 1000 to 1200°C because unburned matter is reburned.

完全燃焼したガスはスラグスクリーン6、一次
過熱器7a、二次過熱器7b、蒸発水管8、節炭
器9および空気予熱器10を経て系外に排出され
る。また以上の各部における温度を示すと一次過
熱器7aの入口(符号Dで示す)においては約
800℃〜1000℃、二次過熱器7bの入口(符号E
で示す)において約650℃〜700℃、二次過熱器7
bの出口(符号Fで示す)においては約550℃〜
650℃となる。
The completely combusted gas passes through the slag screen 6, the primary superheater 7a, the secondary superheater 7b, the evaporative water pipe 8, the economizer 9, and the air preheater 10, and is discharged to the outside of the system. In addition, the temperature at each part above is approximately
800℃~1000℃, inlet of secondary superheater 7b (code E
) at approximately 650℃ to 700℃, secondary superheater 7
Approximately 550℃~ at the outlet of b (indicated by symbol F)
The temperature will be 650℃.

この発明を実施することによりチヤーベツトの
温度を高く保持できるのでスメトル中の薬品の還
元率を高め、かつSOxの排出量を減少させること
ができる。
By carrying out this invention, the temperature of the chartreuse can be maintained high, thereby increasing the reduction rate of chemicals in the smetol and reducing the amount of SOx discharged.

またチヤーベツト形状を理想的な台形に成形保
持できるのでこの点からも還元率を高めることが
できる。
Furthermore, since the chartreuse can be formed and maintained in an ideal trapezoidal shape, the reduction rate can also be increased from this point of view.

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

第1図はこの発明に係る方法を実施するための
回収ボイラの断面図、第2図はチヤーベツト温度
とSO2の排出量の関係を示す線図、第3図は回収
ボイラの温度分布を示す線図である。 1……回収ボイラ本体、3……チヤーベツト。
Figure 1 is a sectional view of a recovery boiler for carrying out the method according to the present invention, Figure 2 is a diagram showing the relationship between chartreuse temperature and SO 2 emissions, and Figure 3 is a diagram showing the temperature distribution of the recovery boiler. It is a line diagram. 1... recovery boiler body, 3... charbet.

Claims (1)

【特許請求の範囲】[Claims] 1 黒液を粗粒状にして炉壁に吹き付け乾燥しチ
ヤーとして炉底に落下させチヤーベツトを形成し
て燃焼させ薬品を回収する回収ボイラを運転する
方法において、炉底近傍に供給する一次空気量を
全空気供給量の約50%とし、二次空気量を全空気
供給量の約30%とし、チヤーベツトの温度を約
1000℃乃至1100℃とし、全空気供給量の約20%の
量の三次空気を供給して排ガス中の未燃成分を燃
焼し、二次空気による燃焼ガス温度を約1200℃乃
至1300℃にして運転することを特徴とする回収ボ
イラの運転方法。
1. In a method of operating a recovery boiler in which black liquor is made into coarse particles, sprayed onto the furnace wall, dried, and dropped to the bottom of the furnace as a char to form a chervet and burn it to recover chemicals, the amount of primary air supplied to the vicinity of the bottom of the furnace is The amount of secondary air should be approximately 50% of the total air supply, the secondary air amount should be approximately 30% of the total air supply, and the temperature of the Charvet should be approximately 50% of the total air supply.
The temperature is 1000℃ to 1100℃, and tertiary air is supplied in an amount of about 20% of the total air supply to burn unburned components in the exhaust gas, and the combustion gas temperature by secondary air is set to about 1200℃ to 1300℃. A method of operating a recovery boiler, which is characterized by operating a recovery boiler.
JP3318881A 1981-03-10 1981-03-10 Operation of recovery boiler Granted JPS57148101A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3318881A JPS57148101A (en) 1981-03-10 1981-03-10 Operation of recovery boiler

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3318881A JPS57148101A (en) 1981-03-10 1981-03-10 Operation of recovery boiler

Publications (2)

Publication Number Publication Date
JPS57148101A JPS57148101A (en) 1982-09-13
JPH0323801B2 true JPH0323801B2 (en) 1991-03-29

Family

ID=12379507

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3318881A Granted JPS57148101A (en) 1981-03-10 1981-03-10 Operation of recovery boiler

Country Status (1)

Country Link
JP (1) JPS57148101A (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51130301A (en) * 1975-05-08 1976-11-12 Kawasaki Heavy Ind Ltd Air supplying device for reagents recovery boiler
JPS5385531A (en) * 1977-01-07 1978-07-28 Mitsubishi Heavy Ind Ltd Soda recovery boiler

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Publication number Publication date
JPS57148101A (en) 1982-09-13

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