JPS5936793A - Method and apparatus for recovering soda from pulp waste liquor - Google Patents
Method and apparatus for recovering soda from pulp waste liquorInfo
- Publication number
- JPS5936793A JPS5936793A JP14213782A JP14213782A JPS5936793A JP S5936793 A JPS5936793 A JP S5936793A JP 14213782 A JP14213782 A JP 14213782A JP 14213782 A JP14213782 A JP 14213782A JP S5936793 A JPS5936793 A JP S5936793A
- Authority
- JP
- Japan
- Prior art keywords
- soda
- recovery boiler
- waste liquid
- pulp waste
- furnace
- 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
Links
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 title claims description 42
- 239000002699 waste material Substances 0.000 title claims description 26
- 238000000034 method Methods 0.000 title claims description 10
- 238000011084 recovery Methods 0.000 claims description 41
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 38
- 239000007788 liquid Substances 0.000 claims description 24
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 19
- 241001062472 Stokellia anisodon Species 0.000 claims description 14
- 239000000843 powder Substances 0.000 claims description 12
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 9
- 238000002485 combustion reaction Methods 0.000 claims description 9
- 239000011575 calcium Substances 0.000 claims description 8
- 239000000292 calcium oxide Substances 0.000 claims description 8
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 7
- 229910052791 calcium Inorganic materials 0.000 claims description 7
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 18
- 238000009993 causticizing Methods 0.000 description 11
- 239000000126 substance Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000010411 cooking Methods 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 239000003513 alkali Substances 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 235000017550 sodium carbonate Nutrition 0.000 description 3
- 235000019738 Limestone Nutrition 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000012717 electrostatic precipitator Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000006028 limestone Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 239000000463 material Substances 0.000 description 1
Landscapes
- Paper (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は、パルプ廃液ソーダ回収方法及び装置の改善、
特に回、収薬品の苛性化プロセスの合理化対策に関する
。DETAILED DESCRIPTION OF THE INVENTION The present invention provides improvements to pulp waste soda recovery methods and devices;
In particular, it concerns measures to streamline the causticization process for recovered chemicals.
第1図のアルカリパルプ製造工程全示す概略説明図を用
δで従来のアルカリパルグ覗造法を説明する。The conventional alkali pulp production method will be explained using δ, which is a schematic explanatory diagram showing the entire alkali pulp production process shown in FIG.
第1図において、1はパルプ蒸解用、2はパルプ材のブ
ロータンク、Pはパルプ、5は廃液を濃縮するためのエ
バポレータ、4は薬品回収ボイラ(以下回収ボイラと呼
ぶ)、5はスメルト溶解タンク、6は苛性化槽、7はロ
ータリキルン、8は白液タンク、9は電気集塵機である
。In Figure 1, 1 is for pulp cooking, 2 is a blow tank for pulp material, P is for pulp, 5 is an evaporator for concentrating waste liquid, 4 is a chemical recovery boiler (hereinafter referred to as recovery boiler), and 5 is for smelt dissolution. 6 is a causticizing tank, 7 is a rotary kiln, 8 is a white liquor tank, and 9 is an electrostatic precipitator.
パルプ蒸解用の薬品は、蒸解缶1又は苛性化槽6に供給
され、以下ブロータンク2、エバポレータ5、回収ボイ
ラ4、スメルト溶解タンク5、苛性化槽6、白液タンク
8の順にパルプ蒸解薬品循環系統PLを循環する。苛性
化槽6で生成した炭酸カルシウムは、ロータリキルン7
で焼成して酸化カルシウムとし苛性化pJJ16に循不
利用される。又、薬品は上記回収ボイラ4において一部
煙道)う・らダストとなって飛散するlJ(、そのほと
んどは電気集塵機9て回収され、て黒液ラインに戻され
」1記回収ボイラ4に送らね、す熱焼される。Pulp cooking chemicals are supplied to the digester 1 or causticizing tank 6, followed by the blow tank 2, evaporator 5, recovery boiler 4, smelt dissolving tank 5, causticizing tank 6, and white liquor tank 8. It circulates through the circulation system PL. The calcium carbonate produced in the causticizing tank 6 is transferred to the rotary kiln 7.
It is calcined to form calcium oxide and recycled for causticization pJJ16. In addition, some of the chemicals in the recovery boiler 4 (part of the flue) are scattered as dust (most of which is collected by the electrostatic precipitator 9 and returned to the black liquor line). Don't send it, it will be roasted hot.
従来の方法において、アルカ1しくルブ廃液は回収ボイ
ラ4で燃焼する。ここで生成したスメルトは、スメルト
溶解槽5で水に溶解して炭酸ソーダ水溶液をつくる。こ
の炭酸ソーダ゛は、苛性化槽6で、供給されるOa (
OHI 2 (又r、10aOと1(20)と接触させ
て次式のように蒸解薬品である苛性ソーダに苛性化され
る0
Na200. + Ca(OH)2 −+
2NaOH+ CaCO3一方、苛性化槽6で
生成し1cac○3は、ロークリキルン7で焼成してC
aOとし、水で消オロさ什てCa(OH1z ’l:生
成させ苛性化槽6に循環1史用する。In the conventional method, the alkaline waste liquid is combusted in a recovery boiler 4. The smelt produced here is dissolved in water in a smelt dissolving tank 5 to produce a sodium carbonate aqueous solution. This sodium carbonate is Oa (
OHI 2 (also r, 10aO and 1(20) are brought into contact and causticized with caustic soda, which is a cooking chemical, as shown in the following formula: 0 Na200. + Ca(OH)2 −+
2NaOH+ CaCO3 On the other hand, 1cac○3 produced in the causticizing tank 6 is calcined in the rotary kiln 7 and converted to C
aO, quenched with water to produce Ca(OH1z'l), and circulated in the causticizing tank 6 for one cycle.
上記従来法の欠点は、苛性化槽6で生成したCaCO3
スラリをキルン焼成するときの燻4斗1史用本発明は苛
性化槽6で生成するCaCO3スラリーの焼成に2ける
省エネ、Iレギーと回収薬品の苛性化プロセスの合理化
を図9うる)(ノトブ廃液ソーダ回収方法及び装置を提
供することを目的とするもので、回収ボイラのパルプ廃
液燃焼部にCaCO3を主として含む粉末を供給して回
収ボイラ炉内にてQaOを焼成させ、同炉内で焼成され
たOaOの大部分を炉壁を流下するスメルトとともに回
収ボイラ下部のソーダ溶解槽へ導きソーダ及びカルシウ
ムを回収するようにし7たことを要旨とするものである
0
これによシ従来使用していた苛性化装置内のCaCO3
粉末を未焼成のまま回収ボイラ燃焼部に投入できる。従
って、CaCO3焼成手段、例えばロータリキルンを排
除でき燃料費を節減できる0本発明の第1の発明は、ソ
ーダ回収ボイラでパルプ廃液を噴霧燃焼する際に、回収
ボイラのパルプ廃液・燃焼部に炭酸カルシウムを主とし
て含む粉末を供給して回収ボイラ炉内にて酸化カルシウ
ムを焼成させ、同炉内で焼成さhた酸化カルシウムの大
部分を炉壁を流下するスメル1トとともに回収ボイラ下
部のソーダ溶解槽へ導きソーダ及びカルシウム全回収す
ることを特徴とするものであり、第2の発明は、パルプ
廃液を噴霧燃焼するソーダ回収ボイラにおいて、回収ボ
イラのパルプ廃液燃焼部に開口するごとく配設された炭
酸力ルンウムを主として含む粉末の供給口と、回収ボイ
ラ下部に配設さねたソーダ及びカルシウム分を回収する
ソーダ溶解槽とからなることを特徴とするものである0
本発明の方法および装置はエネルギー多消費型産業であ
る紙パルプ工場のバルブ蒸jVr薬品回収ボイラに適用
して有効である0
以下、第2図を参照して本発明を説明する0図において
、10は回収ボイラ本体であり、下部は漏斗状に傾請し
ておりスメルトが流下しやすいように形成ざ力、ている
011は煙道に連がるボイラバンク部、12はパルプ廃
液、′クーテ、15及び14はそれぞれ1次及び2次空
気供給口、15(l″j:炭酸カルシウムを主として含
む粉末例えば石灰石CaCO3、ドロマイトCjaCO
3,MSFCO3等の供給口である。なお、上記粉末は
パルプ廃液供給系統に添加してもよい。16は上記回収
ボイラ10の下部に配設されたソーダ溶解槽、17は同
ソーダ溶解槽16の上部に開口するごとく配設された用
水供給口、18は上記ソーダ溶解槽16に開口するごと
く配設された白液取出し管、19は同白液取出し管18
が接続された白液タンク、20は同白液タンク19に接
続された白液供給管、21は上記ソーダ溶解槽16の下
底に接続された炭酸カルシウムスラリ取出し管である。The disadvantage of the above conventional method is that the CaCO3 generated in the causticizing tank 6
The present invention saves energy in the firing of CaCO3 slurry produced in the causticizing tank 6, and streamlines the causticizing process for the I-reggie and recovered chemicals. The purpose is to provide a waste soda recovery method and device, in which powder containing mainly CaCO3 is supplied to the pulp waste liquid combustion section of a recovery boiler, QaO is fired in the recovery boiler furnace, and QaO is fired in the same furnace. The main purpose of this method is to guide most of the OaO that is produced along with the smelt flowing down the furnace wall to the soda dissolving tank at the bottom of the recovery boiler and recover soda and calcium. CaCO3 in the causticizing equipment
The unfired powder can be fed into the recovery boiler combustion section. Therefore, the CaCO3 burning means, for example, a rotary kiln, can be eliminated and fuel costs can be saved.The first aspect of the present invention is that when pulp waste liquid is spray-combusted in a soda recovery boiler, carbon dioxide is added to the pulp waste liquid/combustion section of the recovery boiler. Powder containing mainly calcium is supplied and calcium oxide is calcined in the recovery boiler furnace, and most of the calcined calcium oxide in the furnace is dissolved in soda at the bottom of the recovery boiler along with smelt flowing down the furnace wall. The second invention is a soda recovery boiler that sprays and burns pulp waste liquid, and is arranged so as to open into the pulp waste liquid combustion section of the recovery boiler. The method and apparatus of the present invention are characterized by comprising a supply port for powder mainly containing carbonate, and a soda dissolving tank disposed at the bottom of a recovery boiler to recover waste soda and calcium. This invention is effective when applied to a valve steam jVR chemical recovery boiler in a paper and pulp mill, which is an energy-intensive industry.Hereinafter, the present invention will be explained with reference to FIG. 2.In the figure, 10 is the recovery boiler body. , the lower part is tilted in the shape of a funnel and has a tension formed so that the smelt can easily flow down. 011 is the boiler bank part connected to the flue, 12 is the pulp waste liquid, 'coote, 15 and 14 are each 1 Secondary and secondary air supply ports, 15 (l″j: Powder mainly containing calcium carbonate, such as limestone CaCO3, dolomite CjaCO
3. This is the supply port for MSFCO3, etc. Note that the above powder may be added to the pulp waste liquid supply system. 16 is a soda dissolving tank disposed at the bottom of the recovery boiler 10, 17 is a water supply port disposed to open at the top of the soda dissolving tank 16, and 18 is a water supply port disposed to open to the soda dissolving tank 16. The white liquid take-out pipe 19 is the same white liquid take-out pipe 18.
20 is a white liquor supply pipe connected to the white liquor tank 19, and 21 is a calcium carbonate slurry take-out pipe connected to the bottom of the soda dissolving tank 16.
このような構成において、本発明の作用について説明す
る0回収ボイラ10のパルプ廃液燃焼部である炉底部に
は高濃度に濃縮されたアルカリパルプ廃液が、バーナ1
2から微粒状で噴霧され炉底部に供給される1次及び2
次空気供給管15.14から供給される加熱空気で高温
燃焼されスメルト(主としてNa2C03) ’fr:
生成する。この際、図のように炉底部を漏斗状に傾斜さ
せておきスメルトの流り、 f 、[l好にする。。In such a configuration, highly concentrated alkaline pulp waste liquid is stored in the bottom of the furnace, which is the pulp waste liquid combustion part of the zero recovery boiler 10, which will explain the operation of the present invention.
The primary and secondary components are sprayed in fine particles from 2 and supplied to the bottom of the furnace.
Next, smelt (mainly Na2C03) is burned at high temperature with heated air supplied from air supply pipe 15.14 'fr:
generate. At this time, the bottom of the furnace is tilted in the shape of a funnel as shown in the figure, so that the flow of the smelt is favorable. .
さらに、炉底部に炭酸カルシウムを王として含む粉末、
例えば石灰石CaCO3粉末を供給口15から炉内に噴
射する。炉内で焼成(CaCO3→cao + CO2
)されたCaOの大部分を炉壁を流下するスメルトに乗
せて下部のソーダ溶解槽16に流下させる。ソーダ溶解
槽16内では、用水供給管17からあら刀・じめ供給l
〜である水にスメルト(Na2CO3,Ca0)が溶解
して下記反応を生ずる。Furthermore, powder containing calcium carbonate as the king at the bottom of the furnace,
For example, limestone CaCO3 powder is injected into the furnace from the supply port 15. Calcination in a furnace (CaCO3→cao + CO2
) Most of the dissolved CaO is carried on the smelt flowing down the furnace wall and is caused to flow down into the soda dissolving tank 16 at the bottom. Inside the soda dissolving tank 16, the water is supplied from the water supply pipe 17.
When smelt (Na2CO3, Ca0) is dissolved in water, the following reaction occurs.
Na2003 + OaO+ H2O−) 2NaOH
+ CaCO3とのようにして蒸解薬品であるNaOH
f作る〇一方、ソーダ溶解槽16で生成したNMOHは
白液取出口18力)ら白液タンク19へ導かれ、白液供
給管20から以降第1図に示すようなノくルプ蒸解薬品
循環系統PLへ送られるO又、ソーダ溶解槽16で生成
したO a CO3は炭酸カルシウムスラリ取出口21
から取出される。Na2003 + OaO+ H2O-) 2NaOH
+ NaOH which is a cooking chemical like CaCO3
On the other hand, the NMOH generated in the soda dissolving tank 16 is led to the white liquor tank 19 from the white liquor outlet 18), and from the white liquor supply pipe 20, the NMOH produced in the soda dissolving tank 16 is fed to the white liquor cooking chemicals as shown in Fig. 1. The O a CO3 sent to the circulation system PL and the O a CO3 generated in the soda dissolving tank 16 are sent to the calcium carbonate slurry outlet 21
taken from.
本発明において次のような効果が奏される。The present invention provides the following effects.
(2)本発明方法は、パルプ膠液−を噴霧燃焼するソー
ダ回収ボイラにおいて、回収ボイラのパルプ廃液燃焼部
に炭酸カルシウムを主として含む粉末を供給して回収ボ
イラ炉内にて酸化カルシウム全焼成させるようにし、炉
内で高温を与えて苛性化するようにしたので、従来の方
法に比べ燃料使用量が太きかったロータリキルンによる
加熱が必要でなく、従って燃料費を大幅に節減できる利
点がある。(2) In the method of the present invention, in a soda recovery boiler that sprays and burns pulp glue, powder containing mainly calcium carbonate is supplied to the pulp waste liquid combustion section of the recovery boiler, and calcium oxide is completely burned in the recovery boiler furnace. By applying high temperatures in the furnace to causticize the product, there is no need for heating in a rotary kiln, which requires a large amount of fuel compared to conventional methods, and this has the advantage of significantly reducing fuel costs. be.
(イ)炉内で焼成された酸化カルシウムの大部分を炉壁
を流下するスメルトとともに回収ボイラ下部のソーダ溶
解槽へ導(ようにしたので、融点の高い一0aOも流動
性の良好なNa2CO3スメルトにのせてソーダ溶解槽
−・流1:さぜることができる。CaCO3の分解反応
は890〜900℃程度の加熱だけで反応が進行するの
で有効にソーダ及びカルシウム分を回収することができ
る。(b) Most of the calcium oxide calcined in the furnace is guided to the soda dissolving tank at the bottom of the recovery boiler together with the smelt flowing down the furnace wall. Soda dissolving tank - Stream 1: Can be stirred.The decomposition reaction of CaCO3 proceeds only by heating to about 890-900°C, so soda and calcium can be effectively recovered.
り)技術的な問題点が少ないので無理のないグロセスで
実施できる。ri) Since there are few technical problems, it can be implemented with reasonable effort.
GTニー)本発明装置は、パルプ廃液を噴霧燃焼するソ
ーダ回収ボイラにおいて、回収ボイラのパルプ廃液燃焼
部に開口するごとく炭酸カルシウムを主として含む粉末
を供給する供給口を配設するとともに、回収ボイラ下部
にソーダ及びカルシウム分を回収するソーダ溶解槽を配
設したので、従来装置に比べてスメルト溶解槽、苛性化
槽、ロークリキルンを排除でき製造コスト(i7低減で
きる利点がある。GT knee) The device of the present invention is a soda recovery boiler that spray-combusts pulp waste liquid, in which a supply port for supplying powder mainly containing calcium carbonate is provided so as to open into the pulp waste liquid combustion section of the recovery boiler, and a supply port is provided in the lower part of the recovery boiler. Since a soda dissolving tank is installed to recover soda and calcium, the smelt dissolving tank, causticizing tank, and rotary kiln can be eliminated compared to conventional equipment, which has the advantage of reducing manufacturing costs (i7).
(6) 回収ボイラの炉構造は、アルカリパルプ廃液回
収ボイラと殆んど同じで技術1i11発吸素は、炉底の
一部に限定される利点がある。(6) The furnace structure of the recovery boiler is almost the same as that of the alkaline pulp waste liquid recovery boiler, and the technology 1i11 has the advantage that the absorption is limited to a part of the bottom of the furnace.
第1図は従来のアルカリパルプ製造工a;+j ’f示
f7ゐ−、−41あ、、□2゜、、い、1゜方よおよび
装置を示す概略図である。
復代辺1人 内 1) 明
昭和58年 2 月 デ 日。
特許庁長官 若杉和夫殿
1、事件の表示
昭和57年特許願第142137号
2、 発明y名称 パルプ廃液ソーダ回収方法及び装置
3、補正をする者
事件との関係 特許出願人
住 所 東京都千代田区丸の自重丁目5番1号i”’
; (62o)三菱重工業株式会社(名 相υ
代表者 矢 野 楓
4!x代理人
住 所 東京都港区虎)門−丁目24番11号第二岡田
ビル 電話(504) 1894番氏 名
弁理士(7179) 内 111
明(ほか1名)
2補正の対象
明細書の「発明の詳細な説明」の欄
a補正の内容FIG. 1 is a schematic diagram showing a conventional alkali pulp manufacturing process a; Fukudaibe 1 person 1) February de, 1981. Commissioner of the Japan Patent Office Kazuo Wakasugi1, Indication of the case Patent Application No. 142137 of 19822, Name of the invention Pulp waste liquid soda recovery method and apparatus 3, Relationship with the person making the amendment Patent applicant address Chiyoda-ku, Tokyo Marunojiju-chome 5-1 i"'
(62o) Mitsubishi Heavy Industries, Ltd. (Name: Souyu Representative: Kaede Yano 4!x Agent address: 2nd Okada Building, 24-11 Toramon-chome, Minato-ku, Tokyo Phone: (504) 1894 Name:
Patent attorney (7179) 111
Akira (and 1 other person) 2. Contents of the amendment in column a of “Detailed Description of the Invention” of the specification subject to the amendment
Claims (1)
る際に、回収ボイラのパルプ廃液燃焼部に炭酸力ルシウ
ノ・を主として含む粉末を供給して回収ボイラ炉内にて
酸化カルシウムを焼成させ、同炉内で焼成された酸化カ
ルシウムの大部分を炉壁全流下するスメルトとともに回
収ボイラ下部のソーダ溶解槽へ導きソーダ及びカルシウ
ム分を回収することを特徴とするパルプ廃液ソー・ダ回
収方法。 (2)バルブ廃液を噴霧燃焼するソーダ回収ボイラにお
いて、回収ボイラのパルプ廃液燃焼部に開口するごとぐ
配設された炭酸カルシウムを主として含む粉末の供給口
と、回収ボイラ下部に配設されたソーダ及びカルシウム
分を回収するソーダ溶解槽と力・らなること全特徴とす
るパルプ廃液ソーダ回収装置0[Claims] n) When pulp waste liquid is spray-combusted in a soda recovery boiler, powder containing mainly carbonate is supplied to the pulp waste liquid combustion section of the recovery boiler, and calcium oxide is produced in the recovery boiler furnace. Pulp waste liquid soda is characterized in that most of the calcium oxide calcined in the furnace is guided along with smelt flowing down the entire furnace wall to a soda dissolving tank at the bottom of a recovery boiler to recover soda and calcium content. Collection method. (2) In a soda recovery boiler that spray-combusts valve waste liquid, there is a supply port for powder mainly containing calcium carbonate located right at the opening in the pulp waste liquid combustion section of the recovery boiler, and a soda recovery boiler located at the bottom of the recovery boiler. Pulp waste liquid soda recovery equipment 0, which has all the features of a soda dissolving tank and a soda dissolving tank that recovers the calcium content.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14213782A JPS5936793A (en) | 1982-08-18 | 1982-08-18 | Method and apparatus for recovering soda from pulp waste liquor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14213782A JPS5936793A (en) | 1982-08-18 | 1982-08-18 | Method and apparatus for recovering soda from pulp waste liquor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5936793A true JPS5936793A (en) | 1984-02-29 |
Family
ID=15308222
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14213782A Pending JPS5936793A (en) | 1982-08-18 | 1982-08-18 | Method and apparatus for recovering soda from pulp waste liquor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5936793A (en) |
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-
1982
- 1982-08-18 JP JP14213782A patent/JPS5936793A/en active Pending
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|---|---|---|---|---|
| US10355996B2 (en) | 2012-10-09 | 2019-07-16 | Netspeed Systems | Heterogeneous channel capacities in an interconnect |
| US10496770B2 (en) | 2013-07-25 | 2019-12-03 | Netspeed Systems | System level simulation in Network on Chip architecture |
| US10348563B2 (en) | 2015-02-18 | 2019-07-09 | Netspeed Systems, Inc. | System-on-chip (SoC) optimization through transformation and generation of a network-on-chip (NoC) topology |
| US10452124B2 (en) | 2016-09-12 | 2019-10-22 | Netspeed Systems, Inc. | Systems and methods for facilitating low power on a network-on-chip |
| US10564703B2 (en) | 2016-09-12 | 2020-02-18 | Netspeed Systems, Inc. | Systems and methods for facilitating low power on a network-on-chip |
| US10564704B2 (en) | 2016-09-12 | 2020-02-18 | Netspeed Systems, Inc. | Systems and methods for facilitating low power on a network-on-chip |
| US10523599B2 (en) | 2017-01-10 | 2019-12-31 | Netspeed Systems, Inc. | Buffer sizing of a NoC through machine learning |
| US10419300B2 (en) | 2017-02-01 | 2019-09-17 | Netspeed Systems, Inc. | Cost management against requirements for the generation of a NoC |
| US10469337B2 (en) | 2017-02-01 | 2019-11-05 | Netspeed Systems, Inc. | Cost management against requirements for the generation of a NoC |
| US10469338B2 (en) | 2017-02-01 | 2019-11-05 | Netspeed Systems, Inc. | Cost management against requirements for the generation of a NoC |
| US10547514B2 (en) | 2018-02-22 | 2020-01-28 | Netspeed Systems, Inc. | Automatic crossbar generation and router connections for network-on-chip (NOC) topology generation |
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