JPS641420B2 - - Google Patents

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Publication number
JPS641420B2
JPS641420B2 JP5321680A JP5321680A JPS641420B2 JP S641420 B2 JPS641420 B2 JP S641420B2 JP 5321680 A JP5321680 A JP 5321680A JP 5321680 A JP5321680 A JP 5321680A JP S641420 B2 JPS641420 B2 JP S641420B2
Authority
JP
Japan
Prior art keywords
fluidized bed
gypsum
ash
coal
bed combustion
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
Application number
JP5321680A
Other languages
Japanese (ja)
Other versions
JPS56149369A (en
Inventor
Hiroyuki Matsumura
Tatsusaburo Nakamura
Taisuke Shibata
Tomoaki Takada
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.)
Kawasaki Heavy Industries Ltd
Original Assignee
Kawasaki Heavy Industries Ltd
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 Kawasaki Heavy Industries Ltd filed Critical Kawasaki Heavy Industries Ltd
Priority to JP5321680A priority Critical patent/JPS56149369A/en
Publication of JPS56149369A publication Critical patent/JPS56149369A/en
Publication of JPS641420B2 publication Critical patent/JPS641420B2/ja
Granted legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B18/00Use of agglomerated or waste materials or refuse as fillers for mortars, concrete or artificial stone; Treatment of agglomerated or waste materials or refuse, specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B18/04Waste materials; Refuse
    • C04B18/06Combustion residues, e.g. purification products of smoke, fumes or exhaust gases
    • C04B18/061Ashes from fluidised bed furnaces
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/91Use of waste materials as fillers for mortars or concrete

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Combustion & Propulsion (AREA)
  • Civil Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、燃料である石炭および脱硫剤である
石灰石から構成される流動層における流動層燃焼
の際に発生する石炭灰および使用済脱硫剤からな
る混合粉体を、主原料として硬化体を製造する方
法、詳しくは上記混合粉体を主原料として成形体
を作製し、この成形体を水蒸気で処理することに
より、機械的強度の大きい水和硬化体を製造する
方法に関するものである。 〔従来の技術〕 近年我国においては、1973年の石油危機以来の
国際的な石油供給不安によつて多大なる石油輸入
量の確保が難しくなり、エネルギ需給状態におけ
る石油依存度を小さくするための石油代替エネル
ギの開発が国家的な課題となり、石炭エネルギが
1つの柱としてクローズアツプされている。 石炭を燃料とする際の燃焼方法は、従来微粉炭
燃焼方式が中心であつたが、最近流動層燃焼方式
が注目されている。この流動層燃焼方式は、通常
炉内脱硫方式が採用され、燃料である石炭と、炉
内脱硫のための脱硫剤である石灰石とを投入し、
ボイラ内にて流動層を構成させる方式である。流
動層燃焼方式は、従来の微粉炭燃焼方式に較べ
て、第1に火炉容積が小さくて済み、ボイラ容積
が小さくなること、第2に燃料石炭の品種に関す
る制約が少ないこと、第3に750〜850℃の低温燃
焼が可能であり、灰の凝結に関するトラブルがな
く、サーマルNOxの発生が少ないこと、第4に
伝熱水管表面での総括伝熱係数が大きいこと、な
どの長所を有している。一方、流動層燃焼技術の
実用化の課題として灰処理上の問題がある。流動
層燃焼の際に発生する灰は、いわゆる石炭灰と使
用済脱硫剤とからなり、使用済脱硫剤は脱流生成
物である型無水石こうと、未反応の生石灰とか
ら構成されている。石炭燃焼ガス中の硫黄酸化物
の除去効率、すなわち脱硫率を大きくするため、
通常Ca/Sのモル比が3〜6となるように石灰
石の投入量が設定されており、750〜850℃におけ
る硫黄酸化物との反応により、石灰石が生石灰お
よび型無水石こうとなり、石炭灰とともに排出
される。流動層燃焼灰の発生量は使用石炭の品
種、脱硫率、ボイラの運転条件などにより相当に
異なるが、通常、石炭灰、型無水石こう、生石
灰の発生量はそれぞれ使用石炭量のほぼ15〜20重
量%、1〜10重量%、1〜10重量%である。 従来、我国における発生石炭灰の大部分は微粉
炭燃焼によるものであり、そのうち約10〜20重量
%はフライアツシユとしてセメント混和材、セメ
ント原料などに再利用され、残りは埋立地に廃棄
されていた。しかしながら、セメント原料への再
利用および埋立地への廃棄のいずれにおいても、
将来の石炭灰の大量発生に充分対処し得ることは
期待できないのが現状である。このように微粉炭
燃焼灰においても、石炭灰の処理方法が大きな問
題になりつつあり、流動層燃焼灰についても、石
炭火力発電所などにおける流動層燃焼による本格
的な石炭利用の際に、きわめて多量の流動層燃焼
灰が発生することを考慮すると、流動層燃焼灰と
して、独自の処分方式を確立することが、流動層
燃焼技術の実用化にとつて、きわめて重要な課題
となつている。また流動層燃焼灰の大量処分方式
の確立には、資源としての有効再利用が必須であ
る。これはまず第1に、国産資源の乏しい我国に
おいては、単なる廃棄ではない再利用が、省資
源・省エネルギに直接結びつくこと、第2に、環
境破壊がきわめて少ないことに基づくものであ
る。 従来、特公昭43−21667号公報には、重油焚火
力発電所において石灰石粉末を用いて排ガス中の
SO2を除去した後のダストと、排出石炭灰とを用
いてコンクリートを製造する方法が開示されてい
る。 また特開昭53−1222号公報には、無水石こうに
水酸化カルシウムもしくは酸化カルシウムを加え
て混合したものを第1の原料とし、石炭灰に希硫
酸を加えて混合し乾燥したものを第2の原料とし
て、第1の原料と第2の原料とを混合してセメン
トを製造する方法が開示されている。 〔発明が解決しようとする問題点〕 前記の特公昭43−21667号公報記載の方法にお
いては、混合粉体の割合範囲は示されていない
が、公報第2頁の第1表に示されるように、アツ
シユの割合は配合Aの場合が58.1%{465÷(335
+465)×100}、配合Bの場合が33.3%{306÷
(306+306+306)×100}で、アツシユの割合が比
較的少なく、石炭燃焼時に多量に排出される石炭
灰を処理するのには適していない。また水蒸気で
処理する場合、180℃、10気圧という比較的高温、
高圧の水蒸気を用いている(公報第2頁左欄第17
行)。このようにこの公報記載の方法は、重油焚
火力発電所において脱硫処理した石灰石粉末を有
効利用することを目的としているので、比較的高
温、高圧の水蒸気を使用しても、圧縮強度は40
Kg/cm2、70Kg/cm2(第2頁第2表参照)ときわめ
て低い値にしかならない。 この公報記載の方法においては、上記のよう
に、180℃、10気圧の比較的高温、高圧の蒸気で
養生するものであるから、製造設備としてオート
クレーブが必要であり(公報第2頁左欄17行参
照)、設備が過大となり、連続処理ができないの
でバツチ処理を行わねばならず、石炭灰の大量処
理に不適であり、しかも180℃に維持するための
加熱用エネルギコストが多大となる。 また前記の特開昭53−1222号公報記載の方法に
おいても、混合粉体の割合範囲は示されていない
が、公報第3頁左上欄の実施例に粗粒石炭灰14.9
%、水酸化カルシウム5.0%、無水石こう79.5%
の場合について示され、無水石こうの割合がきわ
めて大きく、石炭灰の割合が少なくなつている。
したがつて石炭燃焼時に多量に排出される石炭灰
を処理するには好ましい方法とは言えない。すな
わち、この公報記載の方法は、無水石こう、水酸
化カルシウム(または酸化カルシウム)、石炭灰、
硫酸を原料とするもので、水和硬化後の2水石こ
うが強度メンバーとなり、石炭灰と硫酸との反応
生成物であるNa2SO4、K2SO4が無水石こうの凝
結促進剤となり、無水石こうが主原料である。一
方、本発明は、石炭灰分、石灰分、石こう分を原
料とするもので、これらの反応生成物(エトリン
ガイト)が強度メンバーとなり、石炭灰が主原料
である。このようにこの公報記載の方法と、本発
明とは強度発現メカニズムが異なつている。また
この公報には成形体を80〜100℃の比較的低温の
常圧水蒸気で処理するという技術的思想は何ら示
唆されていない。 本発明は上記の諸点に鑑みなされたもので、流
動層燃焼灰を土木・建築分野にて資源として大量
に活用すべく、流動層燃焼灰を原料として機械的
強度の大きい水和硬化体を製造する方法を提供す
ることを目的とするものである。 〔問題点を解決するための手段および作用〕 上記の目的を達成するために、本発明の流動層
燃焼灰を主原料とする硬化体の製造方法は、燃料
としての石炭および脱硫剤としての石灰石から構
成される流動層における流動層燃焼の際に発生す
る石炭灰および使用済脱硫剤からなる混合粉体
に、石炭灰分60〜85重量%、石灰分10〜25重量
%、石こう分8〜25重量%の配合割合となるよう
に、生石灰および/または消石灰(以下、生石灰
などという)、ならびに型無水石こう、半水石
こうおよび/または2水石こう(以下、型無水
石こうなどという)を添加・調整し、さらに水を
添加して混練した後、この混練物を型枠または成
形容器を用いて成形し、ついでこの成形体を70〜
100℃の常圧水蒸気で処理するようにしたもので
ある。 本発明の方法において、混水量(粉体100重量
%に対して添加する水の重量%)は、10〜60%、
望ましくは30〜50%である。 以下、本発明の構成を詳細に説明する。一般
に、流動層燃焼灰の代表的性状である成分組成
は、使用する石炭の品種に大きく依存する。まず
第1に、石炭の産出地によつて燃焼残査である
SiO2、Al2O3、CaO、Fe2O3、Na2O、K2Oなどの
成分の配合割合が異なり、第2に、石炭中の硫黄
含有量によつて脱硫生成物である型無水石こう
および未反応の脱硫剤である生石灰の含有量が異
なる。このため流動層燃焼灰を主原料とする水蒸
気処理による高強度の水和硬化体の作製の際に
は、流動層燃焼灰の成分組成によつて、水和硬化
体の適正製造条件は微妙に異なる。主な製造条件
は、必要な際に添加される生石灰などおよび/ま
たは型無水石こうなどの量、流動層燃焼灰の前
処理としての粉砕条件、水蒸気処理条件(温度、
時間)などである。なお水蒸気は、処理装置の強
度などの関係で常圧水蒸気を用いる。 流動層燃焼灰を主原料とする水和硬化体の製造
条件と、水和硬化体の性状との関係は概略つぎの
通りである。水蒸気処理により生成する水和硬化
体の主成分はエトリンガイト(3CaO・AI2O3
3CaSO4・32H2O)、種々の形態のケイ酸カルシ
ウム水和物(XCaO・YSiO2・ZH2O)であるが、
強度メンバーとして最も寄与するものはエトリン
ガイトである。まず原料混合粉体中の型無水石
こう含有量および/または生石灰含有量が少ない
際には、カルシウムモノサルフオアルミネート水
和物(3CaO・Al2O3・CaSO4・12H2O)が主成
分となり、水和硬化体の強度は小さいが、型無
水石こう含有量および/または生石灰含有量が大
きくなるにしたがつて、エトリンガイト量が多く
なり、水和硬化体の強度も大きくなる。さらに
型無水石こうおよび/または生石灰含有量が多く
なると、水蒸気処理時に反応にあずからない遊離
の石こうおよび/または消石灰が生じ、水和硬化
体の強度は低下する。水蒸気処理による水和硬化
体の機械的強度が最も大きくなる最適成分配合
は、生石灰および型無水石こう以外の石炭灰分
60〜85重量%、生石灰分10〜25重量%、型無水
石こう8〜25重量%である。生石灰分および/ま
たは型無水石こう分が最適成分配合より少ない
際には、生石灰分および/または型無水石こう
の添加が必要である。添加の際には、生石灰の代
替として消石灰を用いてもよく、また型無水石
こうの代りに半水石こうまたは/および2水石こ
うを用いてもよい。また流動層燃焼灰の粒度分布
も、水和硬化体の性状に大きな影響を及ぼす。石
炭灰の粒度が小さくなるにしたがつて、すなわち
比表面積が大きくなるにしたがつて、短い処理時
間で水和硬化体は所定の強度を呈する傾向にあ
る。これは流動層燃焼灰を原料とする水蒸気処理
によるエトリンガイトの生成反応は、スルーソル
ーシヨンリアクシヨン(through solution
reaction)であり、エトリンガイトの構成成分の
うちの酸化アルミニウムの溶解度は、他の成分で
ある生石灰、石こうに較べて小さく、エトリンガ
イトの生成速度が、酸化アルミニウムの溶解速度
に依存するためと推定できる。なお消石灰の配合
割合が30重量%を越えると、水蒸気処理後に多く
の消石灰が残り、乾燥雰囲気下では消石灰が炭酸
カルシウムになり、その際の反応膨張によりヘア
クラツク(ミクロクラツク)が多数発生し、製品
性が劣化する。 水蒸気処理条件は処理温度および処理時間が主
な要因である。一般に水蒸気処理時間が短い際に
は、水和硬化体はカルシウムモノサルフオアルミ
ネート水和物、2水石こう、エトリンガイトの混
合物からなり強度は小さく、水蒸気処理時間が長
くなるにしたがつて、エトリンガイトの生成量が
多くなり強度も大きくなる。水蒸気処理を長時間
にわたり実施しエトリンガイトの生成が終結した
後も水蒸気処理を施すと、エトリンガイトは耐熱
性に欠けるため、無水石こうとカルシウムアルミ
ネート水和物に分解し、水和硬化体の強度は低下
する。 上述の如く流動層燃焼灰を主原料とする水和硬
化体の製造条件は、原料となる流動層燃焼灰の性
状に依存するところが大きく、流動層燃焼灰の成
分組成および粒度分布に対応した最も好適な石炭
灰の粉砕条件、生石灰などおよび/または型無
水石こうの添加量、ならびに水蒸気処理条件(処
理温度、処理時間)を選定することが望ましい。 本発明における原料粉体と水とを混練した後、
型枠などの中で成形される水蒸気処理前の成形体
は、短時間の常温養生ではその強度はあまり大き
くなく、取扱いおよび搬送などの際に欠損などの
生じるおそれがある場合には、必要に応じて、水
蒸気処理前の成形体の作製の際に、突き固めプレ
ス成形などにより機械的強度を大きくしておくこ
とも有用である。 本発明の方法において、常圧水蒸気の温度が70
℃未満の場合は、エトリンガイト生成速度が遅い
ため、生成量が少なく、かつ生成結晶が太くな
り、高強度を発現しないという不都合があり、一
方、100℃を越える場合は、エトリンガイトの成
長よりも分解の方が起こりやすいため、生成した
エトリンガイトの分解が起こり、高強度を発現し
ないという不都合がある。 また石灰のうち、消石灰は硬化体を多孔化して
カサ密度を小さくし、生石灰は硬化体を緻密化し
てカサ密度を大きくする作用・効果を有してい
る。 さらに石こうのうち、半水石こうは溶解度が
0.58(β型)、0.45(α型)(g無水物/100g溶液
at50℃)で、混練物は速やかに硬化が進行する。
なお溶液は、石こう飽和水溶液である2水石こう
は溶解度が0.26(g無水物/100g溶液at50℃)
で、混練物は硬化しない。型無水石こうは溶解
度が0.21(g無水物/100g溶液at50℃)で、本発
明のように、硬化促進剤がない場合は硬化せず、
硬化促進剤が存在する場合は、溶解度が高くなり
徐々に硬化するという作用・効果を有している。
したがつて、石こうの種類により、脱型時の成形
体の強度が異なる。 上記のように、石灰、石こうの作用・効果の違
いにより、石炭灰―石灰―石こう混練物の硬化速
度、硬化体のカサ密度、強度が異なる。このた
め、用途によつて異なる要求品質に対応して、石
灰および石こうを使い分ける。 たとえば、硬化体の圧縮強度に着目すれば、石
こうの溶解度との関係が密接であり、生石灰系で
は、同一石炭灰を用いた場合の硬化体の圧縮強度
は、半水石こう系>2水石こう系>型無水石こ
う系となり、消石灰系では、同一石炭灰を用いた
場合の硬化体の圧縮強度は、半水石こう系>2水
石こう系>型無水石こう系となる。 〔実施例〕 つぎに実施例および比較例について説明する。
実施例および比較例における流動層燃焼灰は、燃
料である石炭中の硫黄量に対するカルシウムの
比、すなわちCa/Sがほぼ3.0となるように石灰
石投入量を調節した際の流動層からの排出灰であ
り、2種類の流動層燃焼灰(A)、(B)を使用し
た。これらの燃焼灰(A)、(B)の組成は第1表
に示す如くであり、また燃焼灰(A)の粉砕後の
性状は第2表に示す如くである。
[Industrial Field of Application] The present invention uses a mixed powder consisting of coal ash and spent desulfurization agent generated during fluidized bed combustion in a fluidized bed consisting of coal as a fuel and limestone as a desulfurization agent. A method of producing a cured body as the main raw material, specifically a method of producing a hydrated body with high mechanical strength by producing a molded body using the above-mentioned mixed powder as the main raw material and treating this molded body with steam. It is related to. [Prior art] In recent years, it has become difficult for Japan to secure a large amount of oil imports due to the international oil supply instability since the oil crisis of 1973, and efforts have been made to increase oil imports in order to reduce the dependence on oil in the energy supply and demand situation. The development of alternative energy has become a national issue, with coal energy being highlighted as one of the pillars of energy. Conventionally, pulverized coal combustion has been the main combustion method when coal is used as fuel, but fluidized bed combustion has recently been attracting attention. This fluidized bed combustion method usually uses an in-furnace desulfurization method, in which coal as a fuel and limestone as a desulfurization agent for in-furnace desulfurization are input.
This method creates a fluidized bed within the boiler. Compared to the conventional pulverized coal combustion method, the fluidized bed combustion method requires firstly a smaller furnace volume, which reduces the boiler volume, secondly, there are fewer restrictions regarding the type of fuel coal, and thirdly, the 750 It has the following advantages: low-temperature combustion of ~850℃ is possible, there are no problems with ash condensation, little thermal NOx is generated, and fourthly, the overall heat transfer coefficient on the surface of the heat transfer water tube is large. ing. On the other hand, there is a problem with ash disposal in the practical application of fluidized bed combustion technology. The ash generated during fluidized bed combustion is composed of so-called coal ash and a spent desulfurization agent, and the spent desulfurization agent is composed of type anhydrous gypsum, which is a deflow product, and unreacted quicklime. In order to increase the removal efficiency of sulfur oxides in coal combustion gas, that is, the desulfurization rate,
Usually, the amount of limestone input is set so that the molar ratio of Ca/S is 3 to 6, and by reaction with sulfur oxides at 750 to 850°C, limestone becomes quicklime and type anhydrous gypsum, and together with coal ash. It is discharged. The amount of fluidized bed combustion ash generated varies considerably depending on the type of coal used, desulfurization rate, boiler operating conditions, etc., but normally, the amount of coal ash, type anhydride, and quicklime generated is approximately 15 to 20 times the amount of coal used. % by weight, 1-10% by weight, 1-10% by weight. Previously, most of the coal ash generated in Japan came from pulverized coal combustion, of which approximately 10 to 20% by weight was reused as fly ash for cement admixtures, cement raw materials, etc., and the rest was disposed of in landfills. . However, in both reuse as cement raw materials and disposal in landfills,
The current situation is that it cannot be expected to be able to adequately deal with future large quantities of coal ash. In this way, the treatment method of pulverized coal combustion ash is also becoming a big issue, and fluidized bed combustion ash is also becoming extremely difficult to deal with when full-scale coal is utilized through fluidized bed combustion in coal-fired power plants. Considering that a large amount of fluidized bed combustion ash is generated, establishing a unique disposal method for fluidized bed combustion ash is an extremely important issue for the practical application of fluidized bed combustion technology. Furthermore, in order to establish a mass disposal system for fluidized bed combustion ash, effective reuse as a resource is essential. This is based, firstly, on the fact that in Japan, where domestically produced resources are scarce, reuse rather than mere disposal directly leads to resource and energy conservation, and secondly, there is extremely little environmental destruction. Previously, Japanese Patent Publication No. 43-21667 describes how limestone powder is used to reduce exhaust gas in heavy oil-fired power plants.
A method of producing concrete using dust after removing SO 2 and exhaust coal ash is disclosed. Furthermore, in JP-A-53-1222, the first raw material is a mixture of anhydrous gypsum and calcium hydroxide or calcium oxide, and the second raw material is a mixture of coal ash and dilute sulfuric acid. A method for producing cement by mixing a first raw material and a second raw material is disclosed. [Problems to be solved by the invention] In the method described in the above-mentioned Japanese Patent Publication No. 43-21667, the ratio range of the mixed powder is not indicated, but as shown in Table 1 on page 2 of the publication, In addition, the ratio of thickness is 58.1% for combination A {465 ÷ (335
+465)×100}, 33.3% for combination B {306÷
(306 + 306 + 306) x 100}, the ratio of ash is relatively small, and it is not suitable for processing coal ash, which is emitted in large quantities during coal combustion. In addition, when processing with steam, the temperature is relatively high at 180℃ and 10 atm.
High-pressure steam is used (No. 17, left column, page 2 of the bulletin)
line). As described above, the method described in this publication aims to effectively utilize desulfurized limestone powder in heavy oil-fired power plants, so even if relatively high temperature and high pressure steam is used, the compressive strength is 40%.
Kg/cm 2 , 70Kg/cm 2 (see Table 2 on page 2), which is an extremely low value. In the method described in this publication, as mentioned above, the curing is performed using relatively high-temperature, high-pressure steam at 180°C and 10 atm, so an autoclave is required as manufacturing equipment (page 2, left column 17 of the publication). (see line), the equipment is too large and continuous processing is not possible, so batch processing has to be performed, making it unsuitable for processing large amounts of coal ash.Moreover, the cost of heating energy to maintain the temperature at 180°C is significant. Also, in the method described in the above-mentioned Japanese Patent Application Laid-open No. 1222-1982, the ratio range of the mixed powder is not indicated, but the example in the upper left column of page 3 of the publication shows coarse coal ash 14.9
%, calcium hydroxide 5.0%, anhydrous gypsum 79.5%
The case is shown in which the proportion of anhydrite is extremely large and the proportion of coal ash is small.
Therefore, it cannot be said to be a preferable method for treating coal ash that is emitted in large quantities during coal combustion. That is, the method described in this publication uses anhydrous gypsum, calcium hydroxide (or calcium oxide), coal ash,
It uses sulfuric acid as a raw material, and dihydrate gypsum after hydration hardening becomes the strength member, and Na 2 SO 4 and K 2 SO 4 , which are reaction products of coal ash and sulfuric acid, act as setting accelerators for anhydrous gypsum. Anhydrous gypsum is the main raw material. On the other hand, the present invention uses coal ash, lime, and gypsum as raw materials, the reaction product of these (ettringite) becomes a strength member, and coal ash is the main raw material. As described above, the method described in this publication and the present invention differ in the strength development mechanism. Moreover, this publication does not suggest any technical concept of treating the molded body with normal pressure steam at a relatively low temperature of 80 to 100°C. The present invention was made in view of the above points, and in order to utilize fluidized bed combustion ash in large quantities as a resource in the civil engineering and construction fields, the present invention produces a hydrated and hardened body with high mechanical strength using fluidized bed combustion ash as a raw material. The purpose is to provide a method to do so. [Means and effects for solving the problems] In order to achieve the above object, the method for producing a hardened body using fluidized bed combustion ash as a main raw material according to the present invention uses coal as a fuel and limestone as a desulfurization agent. Coal ash content: 60-85% by weight, lime content: 10-25% by weight, and gypsum content: 8-25% by weight. Add and adjust quicklime and/or slaked lime (hereinafter referred to as quicklime, etc.), and molded anhydrous gypsum, hemihydrate gypsum, and/or dihydrate gypsum (hereinafter referred to as molded anhydrous gypsum, etc.) so that the mixing ratio is % by weight. After further adding water and kneading, this kneaded product is molded using a mold or a molding container, and then this molded product is
It is treated with normal pressure steam at 100℃. In the method of the present invention, the amount of mixed water (weight % of water added to 100 weight % of powder) is 10 to 60%,
Desirably it is 30-50%. Hereinafter, the configuration of the present invention will be explained in detail. Generally, the component composition, which is a typical property of fluidized bed combustion ash, largely depends on the type of coal used. First of all, depending on the place where the coal is produced, there are combustion residues.
The blending ratio of components such as SiO 2 , Al 2 O 3 , CaO, Fe 2 O 3 , Na 2 O, K 2 O is different, and secondly, the type of desulfurization product depends on the sulfur content in the coal. The content of anhydrous gypsum and quicklime, which is an unreacted desulfurization agent, differs. For this reason, when producing high-strength hydrated hardened bodies by steam treatment using fluidized bed combustion ash as the main raw material, the appropriate manufacturing conditions for the hydrated hardened bodies may vary depending on the composition of the fluidized bed combustion ash. different. The main manufacturing conditions are the amount of quicklime and/or molded anhydrous gypsum added when necessary, crushing conditions as a pretreatment for fluidized bed combustion ash, and steam treatment conditions (temperature,
time), etc. Note that atmospheric pressure steam is used as the steam due to the strength of the processing equipment. The relationship between the manufacturing conditions of a hydrated and hardened product using fluidized bed combustion ash as the main raw material and the properties of the hydrated and hardened product is roughly as follows. The main component of the hydrated hardened product produced by steam treatment is ettringite (3CaO・AI 2 O 3
3CaSO 4・32H 2 O), various forms of calcium silicate hydrate (XCaO ・YSiO 2・ZH 2 O),
Ettringite contributes the most as a strength member. First, when the content of anhydrous gypsum and/or quicklime in the raw material mixed powder is low, calcium monosulfur aluminate hydrate (3CaO・Al 2 O 3・CaSO 4・12H 2 O) is the main Although the strength of the hydrated hardened product is low, as the anhydrous gypsum content and/or quicklime content increases, the amount of ettringite increases and the strength of the hydrated hardened product also increases. Furthermore, when the content of anhydrous gypsum and/or quicklime increases, free gypsum and/or slaked lime that does not participate in the reaction occurs during steam treatment, and the strength of the hydrated and hardened product decreases. The optimum composition of ingredients that maximizes the mechanical strength of the hydrated hardened product by steam treatment is coal ash other than quicklime and type anhydrous gypsum.
60-85% by weight, quicklime content 10-25% by weight, and type anhydrous gypsum 8-25% by weight. When the quicklime content and/or the type anhydrous gypsum content is less than the optimum component mix, it is necessary to add the quicklime content and/or the type anhydrous gypsum. When adding, slaked lime may be used instead of quicklime, and hemihydrate gypsum or/and dihydrate gypsum may be used instead of type anhydrous gypsum. Furthermore, the particle size distribution of the fluidized bed combustion ash also has a large effect on the properties of the hydrated hardened product. As the particle size of coal ash becomes smaller, that is, as the specific surface area becomes larger, the hydrated hardened body tends to exhibit a certain strength in a shorter treatment time. This is because the reaction of producing ettringite by steam treatment using fluidized bed combustion ash as a raw material is a through solution reaction.
The solubility of aluminum oxide, one of the constituent components of ettringite, is lower than that of other components such as quicklime and gypsum, and it can be assumed that this is because the rate of formation of ettringite depends on the rate of dissolution of aluminum oxide. If the blending ratio of slaked lime exceeds 30% by weight, a large amount of slaked lime will remain after steam treatment, and in a dry atmosphere, the slaked lime will turn into calcium carbonate, and the reaction expansion will generate many hair cracks (microcracks), resulting in poor product quality. deteriorates. Steam treatment conditions are the main factors of treatment temperature and treatment time. Generally, when the steam treatment time is short, the hydrated hardened product consists of a mixture of calcium monosulfo aluminate hydrate, dihydrate gypsum, and ettringite, and its strength is low; The amount of produced increases and the strength also increases. If steam treatment is carried out for a long time and steam treatment is continued even after the formation of ettringite has been completed, ettringite lacks heat resistance, so it decomposes into anhydrous gypsum and calcium aluminate hydrate, and the strength of the hydrated hardened product decreases. descend. As mentioned above, the manufacturing conditions for hydrated hardened products using fluidized bed combustion ash as the main raw material largely depend on the properties of the fluidized bed combustion ash, which is the raw material. It is desirable to select suitable coal ash pulverization conditions, the amount of added quicklime etc. and/or type anhydrous gypsum, and steam treatment conditions (treatment temperature, treatment time). After kneading the raw material powder and water in the present invention,
The strength of the molded product before steam treatment, which is molded in a formwork etc., is not very high after curing at room temperature for a short time, and if there is a risk of damage during handling or transportation, Accordingly, it is also useful to increase the mechanical strength by tamping press molding or the like when producing a molded body before steam treatment. In the method of the present invention, the temperature of atmospheric pressure steam is 70°C.
If the temperature is below 100°C, the rate of ettringite formation is slow, resulting in a small amount of produced crystals and thick crystals that do not exhibit high strength. Since this is more likely to occur, the generated ettringite will be decomposed and high strength will not be developed. Among the limes, slaked lime has the effect of making the hardened body porous and decreasing the bulk density, and quicklime has the effect of making the hardened body dense and increasing the bulk density. Furthermore, among gypsum, hemihydrate gypsum has a low solubility.
0.58 (β type), 0.45 (α type) (g anhydride/100g solution
at 50°C), the kneaded material rapidly hardens.
The solution is a saturated aqueous solution of gypsum dihydrate, which has a solubility of 0.26 (g anhydride/100g solution at 50°C).
Therefore, the kneaded material does not harden. Type anhydrous gypsum has a solubility of 0.21 (g anhydride/100g solution at 50°C), and as in the present invention, it will not harden if there is no hardening accelerator.
When a curing accelerator is present, it has the effect of increasing solubility and gradually curing.
Therefore, the strength of the molded product upon demolding varies depending on the type of gypsum. As mentioned above, the hardening speed of the coal ash-lime-gypsum mixture, bulk density, and strength of the hardened product differ due to the differences in the actions and effects of lime and gypsum. For this reason, lime and gypsum are used depending on the quality required depending on the application. For example, if we focus on the compressive strength of a hardened product, there is a close relationship with the solubility of gypsum; in a quicklime system, the compressive strength of a hardened product using the same coal ash is For slaked lime systems, the compressive strength of the hardened material when using the same coal ash is as follows: hemihydrate gypsum system > dihydrate gypsum system > type anhydrous gypsum system. [Example] Next, Examples and Comparative Examples will be described.
The fluidized bed combustion ash in the examples and comparative examples is the ash discharged from the fluidized bed when the amount of limestone input is adjusted so that the ratio of calcium to the amount of sulfur in the fuel coal, that is, Ca/S, is approximately 3.0. Two types of fluidized bed combustion ash (A) and (B) were used. The compositions of these combustion ashes (A) and (B) are as shown in Table 1, and the properties of the combustion ashes (A) after pulverization are as shown in Table 2.

【表】【table】

【表】 流動層燃焼灰の化学的成分としては、X線回折
分析によれば石英(α―SiO2)、型無水石こう
(・CaSO4)、生石灰(CaO)などが認められ
た。 流動層燃焼灰および水和硬化体の試験方法をつ
ぎに示す。プレーン比表面積測定は、島津製作所
製の粉体比表面積測定器SS―100形を使用し、空
気透過法によつた。曲げ強度試験は、試験片とし
て20×20×80(mm)のものを使用し、試験装置と
して丸菱科学製作所製のMKS改良型万能強度試
験機を使用した。試験方法は3点曲げ法によつ
た。圧縮強度試験は、試験片として20×20×20
(mm)のものを使用し、試験装置としてインスト
ロン社製の万能試験機(最大荷量10トン)を使用
した。試験方法は定たわみ速度法によつた。 なお実施例および比較例においては、水蒸気は
常圧水蒸気を使用した。 実施例 1 流動層燃焼灰(A)100部、水50部を混合して
スラリーとし、このスラリーを型枠中に注入して
成形体を得た。この成形体を脱型して密閉容器内
に収納し、80℃の水蒸気と15時間接触させて水和
硬化体を得た。水和硬化体の特性は第3表の如く
であつた。 実施例 2 実施例1において得た成形体を97℃の水蒸気と
15時間接触させた。水和硬化体の特性は第3表の
如くであつた。 比較例 1 実施例1において得た成形体を110℃の水蒸気
と15時間接触させた。水和硬化体の特性は第3表
の如くであつた。 比較例 2 実施例1において得た成形体を60℃の水蒸気と
15時間接触させた。水和硬化体の特性は第3表の
如くであつた。 比較例 3 実施例1において得た成形体を水蒸気処理する
ことなく試験した。結果は第3表の如くであつ
た。 実施例 3 流動層燃焼灰(B)90部、半水石こう10部、水
60部を混合してスラリーとし、このスラリーを型
枠中に注入して成形体を得た。この成形体を脱型
して密閉容器内に収納し、75℃の水蒸気と15時間
接触させて水和硬化体を得た。水和硬化体の特性
は第3表の如くであつた。 比較例 4 流動層燃焼灰(B)100部、水60部を混合して
スラリーとし、このスラリーを型枠中に注入して
成形体を得た。この成形体を脱型して密閉容器内
に収納し、75℃の水蒸気と15時間接触させて水和
硬化体を得た。水和硬化体の特性は第3表の如く
であつた。 比較例 5 流動層燃焼灰(B)50部、半水石こう50部、水
60部を混合してスラリーとし、このスラリーを型
枠中に注入して成形体を得た。この成形体を脱型
して密閉容器内に収納し、75℃の水蒸気と15時間
接触させて水和硬化体を得た。水和硬化体の特性
は第3表の如くであつた。 比較例 6 流動層燃焼灰(B)50部、消石灰40部、半水石
こう10部、水60部を混合してスラリーとし、この
スラリーを型枠中に注入して成形体を得た。この
成形体を脱型して密閉容器内に収納し、75℃の水
蒸気と15時間接触させて水和硬化体を得た。水和
硬化体の特性は第3表の如くであつた。
[Table] According to X-ray diffraction analysis, the chemical components of the fluidized bed combustion ash included quartz (α-SiO 2 ), type anhydrous gypsum (・CaSO 4 ), and quicklime (CaO). The test method for fluidized bed combustion ash and hydrated hardened material is shown below. The plain specific surface area measurement was carried out using a powder specific surface area measuring instrument SS-100 manufactured by Shimadzu Corporation, using the air permeation method. In the bending strength test, a 20 x 20 x 80 (mm) test piece was used, and an MKS improved universal strength testing machine manufactured by Marubishi Kagaku Seisakusho was used as the testing device. The test method was a three-point bending method. Compressive strength test uses 20 x 20 x 20 as a test piece
(mm), and a universal testing machine (maximum load: 10 tons) manufactured by Instron was used as the testing device. The test method was based on the constant deflection rate method. Note that in the Examples and Comparative Examples, atmospheric pressure steam was used as the steam. Example 1 100 parts of fluidized bed combustion ash (A) and 50 parts of water were mixed to form a slurry, and this slurry was poured into a mold to obtain a molded body. This molded body was demolded, stored in a closed container, and brought into contact with steam at 80° C. for 15 hours to obtain a hydrated and cured body. The properties of the hydrated and cured product were as shown in Table 3. Example 2 The molded product obtained in Example 1 was heated with steam at 97°C.
Contact was made for 15 hours. The properties of the hydrated and cured product were as shown in Table 3. Comparative Example 1 The molded article obtained in Example 1 was brought into contact with steam at 110° C. for 15 hours. The properties of the hydrated and cured product were as shown in Table 3. Comparative Example 2 The molded product obtained in Example 1 was heated with steam at 60°C.
Contact was made for 15 hours. The properties of the hydrated and cured product were as shown in Table 3. Comparative Example 3 The molded article obtained in Example 1 was tested without steam treatment. The results were as shown in Table 3. Example 3 Fluidized bed combustion ash (B) 90 parts, hemihydrate gypsum 10 parts, water
60 parts were mixed to form a slurry, and this slurry was poured into a mold to obtain a molded body. This molded body was demolded, stored in a closed container, and brought into contact with steam at 75° C. for 15 hours to obtain a hydrated and cured body. The properties of the hydrated and cured product were as shown in Table 3. Comparative Example 4 100 parts of fluidized bed combustion ash (B) and 60 parts of water were mixed to form a slurry, and this slurry was poured into a mold to obtain a molded body. This molded body was demolded, stored in a closed container, and brought into contact with steam at 75° C. for 15 hours to obtain a hydrated and cured body. The properties of the hydrated and cured product were as shown in Table 3. Comparative example 5 Fluidized bed combustion ash (B) 50 parts, hemihydrate gypsum 50 parts, water
60 parts were mixed to form a slurry, and this slurry was poured into a mold to obtain a molded body. This molded body was demolded, stored in a closed container, and brought into contact with steam at 75° C. for 15 hours to obtain a hydrated and cured body. The properties of the hydrated and cured product were as shown in Table 3. Comparative Example 6 50 parts of fluidized bed combustion ash (B), 40 parts of slaked lime, 10 parts of hemihydrate gypsum, and 60 parts of water were mixed to form a slurry, and this slurry was poured into a mold to obtain a molded body. This molded body was demolded, stored in a closed container, and brought into contact with steam at 75° C. for 15 hours to obtain a hydrated and cured body. The properties of the hydrated and cured product were as shown in Table 3.

〔発明の効果〕〔Effect of the invention〕

以上説明したように、本発明の方法において
は、原料中の石炭灰配合割合が60〜85重量%と大
きいため、石炭灰を大量に処理することができ、
また70〜100℃の比較的低温の常圧水蒸気養生で
あるので、オープン構造が可能(加圧密閉構造が
不要)で製造設備が簡素化され、連続養生が可能
で石炭灰の大量処理に適しており、しかも蒸気温
度が100℃以下のため、廃蒸気などの低温蒸気が
使用でき、エネルギコストを低減することができ
る。 そして、本発明の方法によれば、石炭を燃料と
する流動層燃焼の際の排出物である流動層燃焼灰
を主原料として、水蒸気処理によつて高強度の水
和硬化体を容易にかつ安価に製造することが可能
であり、本発明の方法は流動層燃焼灰を有効利用
して土木・建築の分野における各種建材および構
造剤の製造に寄与する技術としてきわめて有益で
ある。
As explained above, in the method of the present invention, since the coal ash blending ratio in the raw material is as high as 60 to 85% by weight, a large amount of coal ash can be processed.
In addition, because atmospheric pressure steam curing is performed at a relatively low temperature of 70 to 100°C, an open structure is possible (no pressurized and sealed structure is required), simplifying manufacturing equipment, and continuous curing is possible, making it suitable for large-scale processing of coal ash. Furthermore, since the steam temperature is below 100°C, low-temperature steam such as waste steam can be used, reducing energy costs. According to the method of the present invention, a high-strength hydrated body can be easily produced by steam treatment using fluidized bed combustion ash, which is an exhaust product from fluidized bed combustion using coal as fuel, as a main raw material. It can be produced at low cost, and the method of the present invention is extremely useful as a technology that contributes to the production of various building materials and structural agents in the fields of civil engineering and construction by effectively utilizing fluidized bed combustion ash.

Claims (1)

【特許請求の範囲】[Claims] 1 燃料としての石炭および脱硫剤としての石灰
石から構成される流動層における流動層燃焼の際
に発生する石炭灰および使用済脱硫剤からなる混
合粉体に、石炭灰分60〜85重量%、石灰分10〜25
重量%、石こう分8〜25重量%の配合割合となる
ように、生石灰および/または消石灰、ならびに
型無水石こう、半水石こうおよび/または2水
石こうを添加・調整し、さらに水を添加して混練
した後、この混練物を型枠または成形容器を用い
て成形し、ついでこの成形体を70〜100℃の常圧
水蒸気で処理することを特徴とする流動層燃焼灰
を主原料とする硬化体の製造方法。
1 A mixed powder consisting of coal ash and spent desulfurization agent generated during fluidized bed combustion in a fluidized bed consisting of coal as a fuel and limestone as a desulfurization agent has a coal ash content of 60 to 85% by weight and a lime content. 10-25
Quicklime and/or slaked lime, as well as type anhydrous gypsum, hemihydrate gypsum and/or dihydrate gypsum are added and adjusted to a blending ratio of 8 to 25% by weight and gypsum content, and water is further added. After kneading, this kneaded product is molded using a mold or a molding container, and the molded product is then treated with atmospheric pressure steam at 70 to 100°C.Curing using fluidized bed combustion ash as the main raw material. How the body is manufactured.
JP5321680A 1980-04-21 1980-04-21 Manufacture of hardened body chiefly based on fluidized bed burnt ash Granted JPS56149369A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5321680A JPS56149369A (en) 1980-04-21 1980-04-21 Manufacture of hardened body chiefly based on fluidized bed burnt ash

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5321680A JPS56149369A (en) 1980-04-21 1980-04-21 Manufacture of hardened body chiefly based on fluidized bed burnt ash

Publications (2)

Publication Number Publication Date
JPS56149369A JPS56149369A (en) 1981-11-19
JPS641420B2 true JPS641420B2 (en) 1989-01-11

Family

ID=12936630

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5321680A Granted JPS56149369A (en) 1980-04-21 1980-04-21 Manufacture of hardened body chiefly based on fluidized bed burnt ash

Country Status (1)

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