Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS6339538B2 - - Google Patents
[go: Go Back, main page]

JPS6339538B2 - - Google Patents

Info

Publication number
JPS6339538B2
JPS6339538B2 JP57176839A JP17683982A JPS6339538B2 JP S6339538 B2 JPS6339538 B2 JP S6339538B2 JP 57176839 A JP57176839 A JP 57176839A JP 17683982 A JP17683982 A JP 17683982A JP S6339538 B2 JPS6339538 B2 JP S6339538B2
Authority
JP
Japan
Prior art keywords
weight
parts
chloride
coal ash
raw material
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
JP57176839A
Other languages
Japanese (ja)
Other versions
JPS5969462A (en
Inventor
Hiroyuki Matsumura
Taisuke Shibata
Toranosuke Hirokawa
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 Motors Ltd
Original Assignee
Kawasaki Jukogyo 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 Kawasaki Jukogyo KK filed Critical Kawasaki Jukogyo KK
Priority to JP57176839A priority Critical patent/JPS5969462A/en
Publication of JPS5969462A publication Critical patent/JPS5969462A/en
Publication of JPS6339538B2 publication Critical patent/JPS6339538B2/ja
Granted legal-status Critical Current

Links

Classifications

    • 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

Landscapes

  • 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、石炭燃焼時に排出される石炭灰を主
原料として硬化体を製造する方法、詳しくは石炭
灰に消石灰または/および生石灰、ならびに2水
石こう、半水石こうまたは/および型無水石こ
うを添加してなる混合粉体を水とともに混練し、
常温養生によつて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、石油依存度を小さくする
ための石油代替エネルギーの開発が国家的な課題
であり、なかでも石炭エネルギーが一つの柱とし
て注目されている。一次エネルギー源としての石
炭の大量消費に対処するための石炭利用技術の実
用化における課題の一つに、石炭燃焼時に発生す
る多量の石炭灰の処理が挙げられる。 石炭燃焼時には通常、石炭使用量のほぼ10〜20
重量%の石炭灰が発生する。通常の微粉炭燃焼ボ
イラより発生するいわゆる微粉炭燃焼灰は、その
発生場所によつてボトムアツシユ、シンダアツシ
ユおよびフライアツシユに区分され、そのうえフ
ライアツシユが発生量の大部分を占める。従来我
国においては、フライアツシユの一部はセメント
混和材、セメント原料などに再利用されており、
残りは埋立地などにて処分されている。 〔発明が解決しようとする問題点〕 しかしながら、現在の方式による再利用だけで
は、将来発生するであろう膨大な石炭灰量に対応
し得るだけの需要量は期待できず、一方、現行の
石炭灰の埋立地などへの処分については、環境規
制の強化に伴い石炭灰処分用地の確保が難しくな
りつつあり、本格的な石炭火力発電所の稼動の際
には、現状の石炭灰の処分方式および有効利用方
式によつて発生する全ての石炭灰を処理すること
は難しくなる見通しである。また石炭灰の大量処
理技術の検討に際しては、環境汚染がなくかつで
きるだけ再利用を志向することが必要である。こ
れは国産資源に乏しく国土が狭隘な我国において
は、単なる投棄処分ではなく石炭灰を資源として
再利用を図ることが重要となるためである。 本発明は上記の諸点に鑑み、石炭灰を海面埋立
および土地造成のための土盤材、軟弱地盤を対象
とする土盤改良材、ならびに道路建設用路盤材な
どの土木部門に大量に活用すべく、石炭灰を原料
として圧縮強度の大きい土盤状硬化体を製造する
ためになされたもので、石炭灰50〜94重量%、望
ましくは60〜80重量%、消石灰または/および生
石灰(以下、消石灰などと略す)5〜40重量%、
望ましくは15〜30重量%、2水石こう、半水石こ
うまたは/および型無水石こう(以下、2水石
こうなとどと略す)1〜40重量%、望ましくは5
〜20重量%からなる混合粉体を原料とし硬化体を
製造する際に、10〜60重量%の混水量(粉体100
重量%に対して添加する水の重量%)の海水にて
該原料粉体を混練した後、または該混合粉体100
重量部に対して0.1〜3重量部の塩化ナトリウム、
塩化カリウム、塩化マグネシウムからなる群から
選ばれた塩化物、および10〜60重量%の混水量の
水を添加し混練した後、この混練物を型枠または
成形容器を用いて所定の形状のもとで常温養生を
施すことにより、またはこの混練物を直接施工対
象箇所に投入し不定形の状態にて常温養生を施す
ことにより、短かい混練時間で圧縮強度の大きい
土盤状硬化体を製造する方法の提供を目的とする
ものである。 〔問題点を解決するための手段および作用〕 上記目的を達成するために、本願の第1の発明
の石炭灰を主原料とする硬化体の製造方法は、石
炭燃焼時に排出される石炭灰50〜94重量%、消石
灰または/および生石灰5〜40重量%、2水石こ
う、半水石こうまたは/および型無水石こう1
〜40重量%からなる混合粉体を原料として硬化体
を製造する際に、該混合粉体100重量部に対して
0.1〜3重量部の塩化ナトリウム、塩化カリウム、
塩化マグネシウムからなる群から選ばれた塩化
物、および10〜60重量%の混水量の水を添加し混
練し、ついでこの混練物を型枠または成形容器な
どを用いて成形した後、常温にて養生することか
らなつている。 また本願の第2の発明の石炭灰を主原料とする
硬化体の製造方法は、石炭燃焼時に排出される石
炭灰50〜94重量%、消石灰または/および生石灰
5〜40重量%、2水石こう、半水石こうまたは/
および型無水石こう1〜40重量%からなる混合
粉体を原料として硬化体を製造する際に、該混合
粉体100重量部に対して0.1〜3重量部の塩化ナト
リウム、塩化カリウム、塩化マグネシウムからな
る群から選ばれた塩化物、および10〜60重量%の
混水量の水を添加し混練し、ついでこの混練物を
特定の形状に成形することなく、常温にて養生す
ることからなつている。 本発明の方法において、混合粉体100重量部に
対して0.1〜3重量部の塩化ナトリウム、塩化カ
リウム、塩化マグネシウムからなる群から選ばれ
たた塩化物、および10〜60重量%の混水量の水と
して、海水を用いるのが望ましい。 以下、本発明の構成を詳細に説明する。一般
に、石炭灰の代表的性状である成分、組成および
粒度分布は石炭の産地および燃焼時の履歴に大き
く依存する。まず第1に、石炭の産出地によつて
SiO2、Al2O3、CaO、Fe2O3、Na2O、K2Oなどの
成分の配合割合が異なり、第2に我国にて現在発
生する石炭灰は微粉炭燃焼灰が主であり、発生場
所および採取方式によつてそれぞれ粒度分布が異
なる。このため、石炭灰を主原料とし常温養生に
よつて圧縮強度の大きい水和硬化体を製造する際
には、石炭灰の組成および粒度分布によつて水和
硬化体の適正製造条件は微妙に異なる。製造条件
として寄与率が大きい要因は、原料粉体の配合割
合、混練時間および混練温度、常温養生時間であ
る。 常温養生によつて生成する水和硬化体の主成分
は、エトリンガイト(3CaO・Al2O3・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、早期の強度
発現に最も寄与するのはエトリンガイトである。
このため、原料粉体の配合割合は、エトリンガイ
トの生成に最も好都合なものが適切であり、消石
灰などの添加量は5〜40重量%、望ましくは15〜
30重量%、2水石こうなどの添加量は1〜40重量
%、望ましくは5〜20重量%に限定される。また
常温養生条件は主として処理時間が主な要因であ
る。常温養生では、エトリンガイトが生成し通常
の土木工事に充分耐えうるための数Kg/cm2以上の
圧縮強度を呈するには通常2、3日〜1週間を要
する。 石炭灰の粒度分布も水和硬化体の性状に大きな
影響をおよぼす。一般に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
にしたがつて短かい養生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、また石炭
灰中に含有されるアルミナ(Al2O3)の溶解速度
が消石灰、2水石こうに較べて著しく小さく、エ
トリンガイトの生成速度はアルミナの溶解速度に
依存すると推定できるためである。このように、
水和硬化体の性状は、石炭灰の成分および組成、
他の原料粉体の添加量、混水量、混練方式および
混練時間、ならびに常温養生期間などの製造条件
によつて大きく影響され、水和硬化体の要求特性
にあわせて各製造条件を適切に選定することが必
要である。 本発明は、各原料粉体の適切なる配合割合から
なる混合粉体と海水とを同時に混練することによ
り、または該混合粉体、水溶性の塩化物および水
とを同時に混練することにより、初期強度の大き
い水和硬化体を簡素な混練工程にて、かつ短かい
混練時間のもとで常温養生を施すことによつて製
造することを目的としたものである。 本発明において、混水量を10〜60重量%として
いるが、混水量を少なくすると強度が高くなるが
成形性が悪くなり、混水量が10重量%程度以下で
は成形できなくなる。また混水量を多くすると流
動性が大きくなつて固化し難くなり、混水量60重
量%程度が限度である。したがつて本発明におい
て、望ましい混水量は30〜50重量%である。 また本発明は、混練水として海水またはこれに
類似する水溶液を使用することにより、水和硬化
体の初期強度の増強および常温養生期間の短縮を
目的としたものである。この水和硬化体の強度発
現はエトリンガイトの生成によるものであるが、
NaCl、KCl、MgCl2などの塩の存在によつてエ
トリンガイトの生成速度が増大し、水和硬化体の
強度が大きくなる。 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原料石炭灰は市販フ
ライアツシユであり、組成および性状を第1表に
示す。
[Industrial Application Field] The present invention relates to a method for producing a hardened material using coal ash discharged during coal combustion as a main raw material. A mixed powder obtained by adding / and molded anhydrous gypsum is kneaded with water,
The present invention relates to a method for producing a hydrated material with high mechanical strength by curing at room temperature. [Prior Art] In recent years, the development of alternative energy to petroleum in order to reduce dependence on petroleum has become a national issue in Japan, and coal energy is attracting attention as one of the pillars of energy. One of the challenges in the practical application of coal utilization technology to cope with the large consumption of coal as a primary energy source is the disposal of large amounts of coal ash generated during coal combustion. When burning coal, usually almost 10 to 20 of the coal usage
% coal ash is generated. The so-called pulverized coal combustion ash generated from a typical pulverized coal combustion boiler is classified into bottom ash, cinder ash, and fly ash depending on where it is generated, and the fly ash accounts for the majority of the amount generated. Traditionally in Japan, a portion of fly ash has been reused as cement admixtures, cement raw materials, etc.
The rest is disposed of in landfills. [Problems to be solved by the invention] However, it cannot be expected that the demand for coal ash will be sufficient to cope with the huge amount of coal ash that will be generated in the future by reusing the current method. As for the disposal of ash in landfills, it is becoming difficult to secure land for coal ash disposal due to stricter environmental regulations. It is expected that it will be difficult to dispose of all of the coal ash generated through this and effective utilization methods. Furthermore, when considering mass processing technology for coal ash, it is necessary to aim for reuse as much as possible without causing environmental pollution. This is because in a country with limited domestic resources and limited land, it is important to reuse coal ash as a resource rather than simply dumping it. In view of the above points, the present invention utilizes coal ash in large quantities in the civil engineering sector, such as as a soil material for sea surface reclamation and land reclamation, as a soil improvement material for soft ground, and as a road base material for road construction. This method was developed to produce a hardened clay body with high compressive strength using coal ash as a raw material, and contains 50 to 94% by weight of coal ash, preferably 60 to 80% by weight, slaked lime or/and quicklime (hereinafter referred to as (abbreviated as slaked lime, etc.) 5 to 40% by weight,
Preferably 15 to 30% by weight, 1 to 40% by weight of dihydrate gypsum, hemihydrate gypsum or/and type anhydrous gypsum (hereinafter abbreviated as dihydrate gypsum), preferably 5
When producing a cured product using a mixed powder of ~20% by weight as raw material, the amount of water mixed in is 10~60% by weight (100% by weight of powder).
After kneading the raw material powder in seawater (wt% of water added to wt%), or after kneading the mixed powder
0.1 to 3 parts by weight of sodium chloride,
After adding and kneading a chloride selected from the group consisting of potassium chloride and magnesium chloride and water in an amount of 10 to 60% by weight, the kneaded product is molded into a predetermined shape using a mold or a molding container. By curing at room temperature with or by directly putting this kneaded material into the construction target area and curing at room temperature in an amorphous state, a hardened soil body with high compressive strength can be produced in a short kneading time. The purpose is to provide a method to do so. [Means and effects for solving the problem] In order to achieve the above object, the method for producing a hardened body using coal ash as a main raw material according to the first invention of the present application uses 50% of coal ash discharged during coal combustion. ~94% by weight, slaked lime or/and quicklime 5-40% by weight, dihydrate gypsum, hemihydrate gypsum or/and type anhydrous gypsum 1
When producing a cured body using a mixed powder consisting of ~40% by weight as a raw material, for 100 parts by weight of the mixed powder.
0.1 to 3 parts by weight of sodium chloride, potassium chloride,
A chloride selected from the group consisting of magnesium chloride and water in an amount of 10 to 60% by weight are added and kneaded, then this kneaded product is molded using a mold or a molding container, and then left at room temperature. It comes from taking care of yourself. Further, the method for producing a hardened body using coal ash as a main raw material according to the second invention of the present application includes 50 to 94% by weight of coal ash discharged during coal combustion, 5 to 40% by weight of slaked lime or/and quicklime, and dihydrate gypsum. , hemihydrate gypsum or/
When producing a hardened body using a mixed powder consisting of 1 to 40% by weight of anhydrous gypsum and type anhydrous gypsum as a raw material, 0.1 to 3 parts by weight of sodium chloride, potassium chloride, and magnesium chloride are added to 100 parts by weight of the mixed powder. The method consists of adding and kneading a chloride selected from the group consisting of: and water in an amount of 10 to 60% by weight, and then curing the kneaded product at room temperature without shaping it into a specific shape. . In the method of the present invention, 0.1 to 3 parts by weight of a chloride selected from the group consisting of sodium chloride, potassium chloride, and magnesium chloride and 10 to 60% by weight of water are added to 100 parts by weight of the mixed powder. It is preferable to use seawater as the water. Hereinafter, the configuration of the present invention will be explained in detail. In general, the typical properties of coal ash, such as components, composition, and particle size distribution, greatly depend on the coal's production area and combustion history. First of all, it depends on the place where the coal is produced.
The proportions of ingredients such as SiO 2 , Al 2 O 3 , CaO, Fe 2 O 3 , Na 2 O, K 2 O are different, and secondly, the coal ash currently generated in Japan is mainly pulverized coal combustion ash. Yes, the particle size distribution varies depending on the location and collection method. Therefore, when producing a hydrated material with high compressive strength using coal ash as the main raw material and curing at room temperature, the appropriate manufacturing conditions for the hydrated material may vary depending on the composition and particle size distribution of the coal ash. different. Factors that have a large contribution rate as manufacturing conditions are the mixing ratio of raw material powder, kneading time and kneading temperature, and room temperature curing time. The main component of the hydrated hardened material produced by curing at room temperature is ettringite (3CaO・Al2O33CaSO4
32H 2 O) and various forms of calcium silicate hydrate (xCaO・ySiO 2・zH 2 O), but the one that contributes most to early strength development is ettringite.
For this reason, the appropriate mixing ratio of the raw material powder is the one most favorable for the production of ettringite, and the amount of slaked lime etc. to be added is 5 to 40% by weight, preferably 15 to 40% by weight.
30% by weight, and the amount of dihydrate gypsum added is limited to 1 to 40% by weight, preferably 5 to 20% by weight. Furthermore, the room temperature curing conditions are mainly due to the processing time. When cured at room temperature, it usually takes a few days to a week for ettringite to form and exhibit a compressive strength of several kg/cm 2 or more, which is sufficient to withstand normal civil engineering work. The particle size distribution of coal ash also has a large effect on the properties of the hydrated hardened material. Generally, as the particle size of coal ash becomes smaller, that is, as the specific surface area becomes larger, the hydrated hardened material tends to exhibit a predetermined strength with a shorter curing time. This is because the formation reaction of ettringite is a through solution reaction, and the dissolution rate of alumina (Al 2 O 3 ) contained in coal ash is significantly lower than that of slaked lime and dihydrate gypsum. This is because it can be estimated that the production rate of ettringite depends on the dissolution rate of alumina. in this way,
The properties of the hydrated hardened product are determined by the components and composition of the coal ash,
It is greatly influenced by manufacturing conditions such as the amount of other raw material powders added, amount of water mixed, kneading method and kneading time, and room temperature curing period, and each manufacturing condition must be appropriately selected according to the required characteristics of the hydrated product. It is necessary to. In the present invention, by simultaneously kneading a mixed powder consisting of an appropriate blending ratio of each raw material powder and seawater, or by simultaneously kneading the mixed powder, a water-soluble chloride, and water, the initial The purpose is to produce a hydrated hardened product with high strength through a simple kneading process and by curing at room temperature under a short kneading time. In the present invention, the amount of mixed water is 10 to 60% by weight, but if the amount of mixed water is reduced, the strength will increase, but the moldability will deteriorate, and if the amount of mixed water is less than about 10% by weight, molding will not be possible. In addition, when the amount of mixed water is increased, the fluidity increases and it becomes difficult to solidify, and the amount of mixed water is about 60% by weight as the limit. Therefore, in the present invention, the desirable amount of water to be mixed is 30 to 50% by weight. Further, the present invention aims at increasing the initial strength of the hydrated and hardened product and shortening the room temperature curing period by using seawater or a similar aqueous solution as the kneading water. The strength of this hydrated hardened product is due to the formation of ettringite,
The presence of salts such as NaCl, KCl, MgCl 2 increases the rate of ettringite formation and increases the strength of the hydrated hardened product. Next, Examples and Comparative Examples will be described.
The raw material coal ash in Examples and Comparative Examples is commercially available fly ash, and the composition and properties are shown in Table 1.

【表】 石炭灰および水和硬化体の試験方法を次に示
す。ブ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、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を使用
した。試験方法は定たわみ法によつた。実施例お
よび比較例においては、常温養生は直射目光をう
けない室内にて実施した。実施例および比較例の
詳細を第2表に示す。 実施例 1 石炭灰85部、消石灰10部、2水石こう5部、海
水40部を同時に混練してスラリーとし、このスラ
リーを室内で7日間常温養生して水和硬化体を得
た。水和硬化体の特性は第2表のごとくであつ
た。 比較例 1 石炭灰85部、消石灰10部、2水石こう5部、水
道水40部を同時に混練してスラリーとし、このス
ラリーを室内で7日間常温養生して水和硬化体を
得た。水和硬化体の特性は第2表のごとくであつ
た。 実施例 2 石炭灰85部、消石灰10部、2水石こう5部、
NaCl1.0部、水道水40部を同時に混練してスラリ
ーとし、このスラリーを室内で7日間常温養生し
て水和硬化体を得た。水和硬化体の特性は第2表
のごとくであつた。 実施例 3 石炭灰85部、消石灰10部、2水石こう5部、
MgCl21.0部、水道水40部を同時に混練してスラ
リーとし、このスラリーを室内で7日間常温養生
して水和硬化体を得た。水和硬化体の特性は第2
表のごとくであつた。 比較例 2 石炭灰85部、消石灰10部、2水石こう5部、
CaCl21.0部、水道水40部を同時に混練してスラリ
ーとし、このスラリーを室内で7日間常温養生し
て水和硬化体を得た。水和硬化体の特性は第2表
のごとくであつた。
[Table] The test methods for coal ash and hydrated hardened bodies are shown below. The Blaine specific surface area was measured using a powder specific surface area measuring instrument SS-100 manufactured by Shimadzu Corporation, using the air permeation method. Bending strength test uses 20×20 as a test piece
For the compressive strength test, a 20 x 20 x 20 (mm) test piece was used as the test piece, and a universal testing machine manufactured by Instron was used as the testing device. The test method was based on the constant deflection method. In the Examples and Comparative Examples, room temperature curing was carried out indoors away from direct sunlight. Details of Examples and Comparative Examples are shown in Table 2. Example 1 85 parts of coal ash, 10 parts of slaked lime, 5 parts of dihydrate gypsum, and 40 parts of seawater were simultaneously kneaded to form a slurry, and this slurry was cured at room temperature for 7 days to obtain a hydrated hardened product. The properties of the hydrated and cured product were as shown in Table 2. Comparative Example 1 85 parts of coal ash, 10 parts of slaked lime, 5 parts of dihydrate gypsum, and 40 parts of tap water were simultaneously kneaded to form a slurry, and this slurry was cured at room temperature for 7 days to obtain a hydrated hardened product. The properties of the hydrated and cured product were as shown in Table 2. Example 2 85 parts of coal ash, 10 parts of slaked lime, 5 parts of dihydrate gypsum,
1.0 part of NaCl and 40 parts of tap water were simultaneously kneaded to form a slurry, and this slurry was cured at room temperature for 7 days to obtain a hydrated hardened product. The properties of the hydrated and cured product were as shown in Table 2. Example 3 85 parts of coal ash, 10 parts of slaked lime, 5 parts of dihydrate gypsum,
1.0 parts of MgCl 2 and 40 parts of tap water were simultaneously kneaded to form a slurry, and this slurry was cured at room temperature for 7 days to obtain a hydrated hardened product. The characteristics of the hydrated hardened product are the second
It was as shown in the table. Comparative Example 2 85 parts of coal ash, 10 parts of slaked lime, 5 parts of dihydrate gypsum,
1.0 part of CaCl 2 and 40 parts of tap water were simultaneously kneaded to form a slurry, and this slurry was cured at room temperature for 7 days to obtain a hydrated hardened product. The properties of the hydrated and cured product were as shown in Table 2.

〔発明の効果〕〔Effect of the invention〕

以上説明したように、本発明によれば石炭燃焼
時の排出物である石炭灰、安価な原料である消石
灰または/および生石灰、2水石こう、半水石こ
うまたは/および型無水石こうを使用し、海水
またはこれに類似した水溶液にて混練した後に常
温養生を施すことによつて圧縮強度の大きい水和
硬化体を容易にかつ安価に製造することが可能で
あり、本発明は石炭灰を有効に活用し土木・建築
の分野における埋立、土地造成、道路建設等のた
めの土盤材などの製造に寄与する技術として有益
である。また本発明の方法は、原料粉体と海水ま
たはこれに類似した水溶液とを同時に混練するの
で、工程がきわめて単純化され、かつ混練時間が
短縮され、水和硬化体をより低コストで製造する
ことができるという効果を有している。
As explained above, according to the present invention, coal ash, which is an exhaust product during coal combustion, slaked lime and/or quicklime, which is an inexpensive raw material, dihydrate gypsum, hemihydrate gypsum, and/or type anhydrous gypsum are used, By kneading in seawater or a similar aqueous solution and then curing at room temperature, it is possible to easily and inexpensively produce a hydrated material with high compressive strength. It is useful as a technology that contributes to the production of soil materials for reclamation, land reclamation, road construction, etc. in the fields of civil engineering and construction. Furthermore, since the method of the present invention simultaneously kneads the raw material powder and seawater or a similar aqueous solution, the process is extremely simplified, the kneading time is shortened, and the hydrated hardened product can be produced at a lower cost. It has the effect of being able to

Claims (1)

【特許請求の範囲】 1 石炭燃焼時に排出される石炭灰50〜94重量
%、消石灰または/および生石灰5〜40重量%、
2水石こう、半水石こうまたは/および型無水
石こう1〜40重量%からなる混合粉体を原料とし
て硬化体を製造する際に、該混合粉体100重量部
に対して0.1〜3重量部の塩化ナトリウム、塩化
カリウム、塩化マグネシウムからなる群から選ば
れた塩化物、および10〜60重量%の混水量の水を
添加し混練し、ついでこの混練物を型枠または成
形容器などを用いて成形した後、常温にて養生す
ることを特徴とする石炭灰を主原料とする硬化体
の製造方法。 2 混合粉体100重量部に対して0.1〜3重量部の
塩化ナトリウム、塩化カリウム、塩化マグネシウ
ムからなる群から選ばれた塩化物、および10〜60
重量%の混水量の水として、海水を用いる特許請
求の範囲第1項記載の石炭灰を主原料とする硬化
体の製造方法。 3 石炭燃焼時に排出される石炭灰50〜94重量
%、消石灰または/および生石灰5〜40重量%、
2水石こう、半水石こうまたは/および型無水
石こう1〜40重量%からなる混合粉体を原料とし
て硬化体を製造する際に、該混合粉体100重量部
に対して0.1〜3重量部の塩化ナトリウム、塩化
カリウム、塩化マグネシウムからなる群から選ば
れた塩化物、および10〜60重量%の混水量の水を
添加し混練し、ついでこの混練物を特定の形状に
成形することなく、常温にて養生することを特徴
とする石炭灰を主原料とする硬化体の製造方法。 4 混合粉体100重量部に対して0.1〜3重量部の
塩化ナトリウム、塩化カリウム、塩化マグネシウ
ムからなる群から選ばれた塩化物、および10〜60
重量%の混水量の水として、海水を用いる特許請
求の範囲第3項記載の石炭灰を主原料とする硬化
体の製造方法。
[Claims] 1. 50-94% by weight of coal ash discharged during coal combustion, 5-40% by weight of slaked lime or/and quicklime,
When producing a hardened body using a mixed powder consisting of 1 to 40% by weight of dihydrate gypsum, hemihydrate gypsum, or/and type anhydrous gypsum as a raw material, 0.1 to 3 parts by weight per 100 parts by weight of the mixed powder. A chloride selected from the group consisting of sodium chloride, potassium chloride, and magnesium chloride and water in an amount of 10 to 60% by weight are added and kneaded, and then this kneaded product is molded using a mold or a molding container. A method for producing a hardened product using coal ash as a main raw material, which is characterized by curing at room temperature after curing at room temperature. 2. Chloride selected from the group consisting of sodium chloride, potassium chloride, magnesium chloride in an amount of 0.1 to 3 parts by weight per 100 parts by weight of the mixed powder, and 10 to 60 parts by weight
2. A method for producing a hardened body using coal ash as a main raw material according to claim 1, wherein seawater is used as the water in the amount of water mixed in % by weight. 3 50-94% by weight of coal ash discharged during coal combustion, 5-40% by weight of slaked lime or/and quicklime,
When producing a hardened body using a mixed powder consisting of 1 to 40% by weight of dihydrate gypsum, hemihydrate gypsum, or/and type anhydrous gypsum as a raw material, 0.1 to 3 parts by weight per 100 parts by weight of the mixed powder. A chloride selected from the group consisting of sodium chloride, potassium chloride, and magnesium chloride and water in an amount of 10 to 60% by weight are added and kneaded, and then the kneaded product is heated at room temperature without forming it into a specific shape. A method for producing a hardened material using coal ash as a main raw material, which is characterized by curing in a . 4 0.1 to 3 parts by weight of a chloride selected from the group consisting of sodium chloride, potassium chloride, and magnesium chloride per 100 parts by weight of the mixed powder, and 10 to 60 parts by weight
4. The method for producing a hardened body using coal ash as a main raw material according to claim 3, wherein seawater is used as the water in the weight percent water content.
JP57176839A 1982-10-06 1982-10-06 Manufacture of hardened body from coal ash Granted JPS5969462A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57176839A JPS5969462A (en) 1982-10-06 1982-10-06 Manufacture of hardened body from coal ash

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57176839A JPS5969462A (en) 1982-10-06 1982-10-06 Manufacture of hardened body from coal ash

Publications (2)

Publication Number Publication Date
JPS5969462A JPS5969462A (en) 1984-04-19
JPS6339538B2 true JPS6339538B2 (en) 1988-08-05

Family

ID=16020729

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57176839A Granted JPS5969462A (en) 1982-10-06 1982-10-06 Manufacture of hardened body from coal ash

Country Status (1)

Country Link
JP (1) JPS5969462A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2711455B2 (en) * 1988-06-27 1998-02-10 株式会社ナカボーテック Backfill for cathodic protection
FR2860789B1 (en) * 2003-10-13 2006-11-24 Rech S Sur Les Materiaux L E R COMPOSITION BASED ON BINDERS CURABLE TO WATER OR AIR AND ITS APPLICATION IN PARTICULAR TO OBTAINING A PRODUCT HAVING THE APPEARANCE AND PROPERTIES OF A NATURAL STONE.

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54143435A (en) * 1978-04-28 1979-11-08 Matsushita Electric Works Ltd Production of inorganic cured body
JPS5924749B2 (en) * 1980-05-02 1984-06-12 川崎重工業株式会社 Method for producing hardened material using coal ash as main raw material

Also Published As

Publication number Publication date
JPS5969462A (en) 1984-04-19

Similar Documents

Publication Publication Date Title
Singh et al. Phosphogypsum—Fly ash cementitious binder—Its hydration and strength development
CN105800979B (en) A kind of good magnesium phosphate cement of water resistance and its application method
CN101367635A (en) All-solid waste low-grade concrete material prepared by using fluidized bed coal-fired sulfur-fixed ash
CN112888664A (en) Coagulation controllable high strength class C fly ash cementitious compositions
KR20240047715A (en) Concrete block composition containing calcium carbonate and manufacturing method thereof
CN109896770A (en) A kind of concrete intensifier
JP6292257B2 (en) Hydrated solidified product using desulfurized slag
CN110615660A (en) Method for preparing pavement rapid repair material by utilizing waste incineration fly ash
JP4663999B2 (en) Soil neutral solidification material and soil neutral solidification improvement method
JPS5953229B2 (en) Method for producing hardened material using coal ash as main raw material
JPS6339538B2 (en)
JP6922448B2 (en) Coal ash composition
JPH0244781B2 (en)
JPS6256097B2 (en)
JPS6324941B2 (en)
JPS6125673B2 (en)
JPS641416B2 (en)
JPS5924749B2 (en) Method for producing hardened material using coal ash as main raw material
JPS5953227B2 (en) Method for producing hardened material using coal ash as main raw material
JPS5953230B2 (en) Method for producing hardened material using coal ash as main raw material
JP2004115291A (en) Solidified body using coal ash, and method of producing the same
JPS641418B2 (en)
JPS641419B2 (en)
JPS641423B2 (en)
JPS641417B2 (en)