JP3440293B2 - Foam using incinerated ash slag glass - Google Patents

Foam using incinerated ash slag glass

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Publication number
JP3440293B2
JP3440293B2 JP36333997A JP36333997A JP3440293B2 JP 3440293 B2 JP3440293 B2 JP 3440293B2 JP 36333997 A JP36333997 A JP 36333997A JP 36333997 A JP36333997 A JP 36333997A JP 3440293 B2 JP3440293 B2 JP 3440293B2
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JP
Japan
Prior art keywords
glass
slag glass
foam material
clay
slag
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
JP36333997A
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Japanese (ja)
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JPH11171661A (en
Inventor
千尋 酒井
剛朗 山音
哲 本田
Original Assignee
経済産業大臣
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    • 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
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/62204Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products using waste materials or refuse
    • 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
    • C04B30/00Compositions for artificial stone, not containing binders
    • 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
    • C04B33/00Clay-wares
    • C04B33/02Preparing or treating the raw materials individually or as batches
    • C04B33/13Compounding ingredients
    • 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
    • C04B33/00Clay-wares
    • C04B33/02Preparing or treating the raw materials individually or as batches
    • C04B33/13Compounding ingredients
    • C04B33/132Waste materials; Refuse; Residues
    • C04B33/135Combustion residues, e.g. fly ash, incineration waste
    • 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
    • C04B33/00Clay-wares
    • C04B33/32Burning methods
    • 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
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/62605Treating the starting powders individually or as mixtures
    • C04B35/62625Wet mixtures
    • C04B35/6263Wet mixtures characterised by their solids loadings, i.e. the percentage of solids
    • 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
    • C04B38/00Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/02Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by adding chemical blowing agents
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3201Alkali metal oxides or oxide-forming salts thereof
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    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3205Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
    • C04B2235/3206Magnesium oxides or oxide-forming salts thereof
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    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3205Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
    • C04B2235/3208Calcium oxide or oxide-forming salts thereof, e.g. lime
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    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/36Glass starting materials for making ceramics, e.g. silica glass
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    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/656Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
    • C04B2235/6562Heating rate
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    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/656Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
    • C04B2235/6565Cooling rate
    • 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
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P40/00Technologies relating to the processing of minerals
    • Y02P40/60Production of ceramic materials or ceramic elements, e.g. substitution of clay or shale by alternative raw materials, e.g. ashes
    • 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

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、下水汚泥や都市ゴ
ミの焼却で多量に発生する焼却灰(以下「ゴミ焼却灰」
と称す。)をガラス化したスラグガラスを有効利用して
得られる発泡材に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to incineration ash (hereinafter referred to as "garbage incineration ash"), which is generated in large amounts by incineration of sewage sludge and municipal waste.
Called. The present invention relates to a foam material obtained by effectively using slag glass obtained by vitrifying

【0002】[0002]

【従来の技術】ゴミ焼却灰は多くの都市で大量に発生し
ており、一般的には地中への埋設などで処分されている
が、処分地の不足から、その減容化が望まれている。ま
た、近年盛んにいわれている資源の有効利用や再利用、
あるいは環境汚染の防止のためにも、これらのゴミ焼却
灰の絶対量を低減させる必要がある。
2. Description of the Related Art A large amount of refuse incinerated ash is generated in many cities and is generally disposed of by burying it in the ground. However, due to the shortage of disposal sites, it is desirable to reduce the volume. ing. In addition, the effective use and reuse of resources, which have been prosperous in recent years,
Alternatively, in order to prevent environmental pollution, it is necessary to reduce the absolute amount of these refuse incineration ash.

【0003】従来、ゴミ焼却灰の再利用のために、ゴミ
焼却灰を還元溶融してスラグガラス化することが進めら
れ、スラグガラスの粉砕物から建材等として有効利用可
能な発泡材を製造する試みがなされている。
Conventionally, in order to reuse the refuse incineration ash, reduction and melting of the refuse incineration ash to form a slag glass has been promoted, and a foam material that can be effectively used as a building material or the like is produced from a crushed product of the slag glass. Attempts are being made.

【0004】即ち、ゴミ焼却灰から製造されたスラグガ
ラスの粉砕物と粘土及び必要に応じて発泡を促進させる
添加剤を混合し、更に水を添加混練して得られた混練物
を800℃以上の温度域で焼成すると、焼成過程におい
て、含有されるガス物質や酸化還元反応に伴うガス成分
の放出、さらにはガラス相の高温条件下での軟化の促進
によって発泡が始まり、温度の上昇に伴ってこの発泡量
は急激に増加し、発泡材が得られる。この発泡材は、そ
の気泡構造を利用した軽量防音材、断熱材等として有用
である。
That is, a crushed product of slag glass produced from waste incineration ash, clay and, if necessary, an additive that promotes foaming are mixed, and water is added and kneaded to obtain a kneaded product of 800 ° C. or higher. When fired in the temperature range of, the foaming begins in the firing process due to the release of the gas substances contained and the gas components accompanying the redox reaction, and further the promotion of softening of the glass phase under high temperature conditions The foaming amount of the lever increases rapidly, and a foam material is obtained. This foam material is useful as a lightweight soundproofing material, a heat insulating material or the like utilizing the cell structure.

【0005】[0005]

【発明が解決しようとする課題】しかし、このようにス
ラグガラスの粉砕物と粘土の混合物を焼成、発泡する場
合、その発泡量が、場合により大きく異なり、所望の発
泡量、即ち、所望の比重及び気孔率の発泡材を安定して
製造することができないという不具合がある。
However, when the mixture of crushed slag glass and clay is fired and foamed as described above, the foaming amount greatly differs depending on the case, and the desired foaming amount, that is, the desired specific gravity is obtained. In addition, there is a problem that a foam material having a porosity cannot be stably manufactured.

【0006】これは、スラグガラスの原料である汚泥や
都市ゴミの組成が一定でないために、スラグガラスの組
成も発生場所、発生時期等により大きく異なるものとな
り、このために、スラグガラス中の発泡の温度とガラス
の軟化の温度域が大きく異なり、発泡後にガラスが軟化
するタイミングがずれることによる。
This is because the composition of sludge and municipal waste, which are the raw materials of slag glass, is not constant, and the composition of slag glass also greatly differs depending on the place of occurrence, the time of occurrence, etc. This is because the temperature and the softening temperature range of the glass are greatly different, and the timing of softening the glass after foaming is deviated.

【0007】このため、発泡性のよいものでは焼成前の
体積に比べて2倍以上の体積の発泡材を得ることができ
るが、発泡倍率が焼成前の1.5倍以下の著しく小さな
ものが形成される場合も多く、所望の発泡材を工業的に
安定生産することができない状況にある。
For this reason, a foam material having a good foaming property can obtain a foam material having a volume two times or more that of the volume before firing, but a foam material having a remarkably small expansion ratio of 1.5 times or less before firing. In many cases, it is formed, and the desired foam material cannot be industrially stably produced.

【0008】本発明は上記従来の問題点を解決し、発泡
量の安定した発泡材を提供することを目的とする。
An object of the present invention is to solve the above conventional problems and provide a foam material having a stable foaming amount.

【0009】[0009]

【課題を解決するための手段】本発明の焼却灰スラグガ
ラスを用いた発泡材は、ゴミ焼却灰をガラス化して得ら
れるスラグガラスの粉砕物と粘土とを混合し、得られた
混合物を焼成して得られる発泡材において、該混合物に
炭酸ナトリウムを、スラグガラスの粉砕物に対して0.
5〜10.0重量%添加した発泡材であって、該スラグ
ガラスの粉砕物に対する炭酸ナトリウムと粘土との合計
の割合が15.0〜30.0重量%であることを特徴と
する。
The foam material using the incinerated ash slag glass of the present invention is a mixture of crushed slag glass obtained by vitrifying refuse incinerated ash and clay, and firing the resulting mixture. In the foamed material obtained in this way, sodium carbonate was added to the mixture, and the mixture was added to the crushed slag glass in an amount of 0.
A foam material containing 5 to 10.0% by weight of the slag
Sum of sodium carbonate and clay for ground glass
Is 15.0 to 30.0% by weight .

【0010】スラグガラスと粘土との混合物を焼成する
ことによる発泡反応機構は次の通りである。
The foaming reaction mechanism by firing the mixture of slag glass and clay is as follows.

【0011】ゴミ焼却灰から製造されたスラグガラス
は、基本的には還元状態での溶解のために、製造された
ガラス内部に酸化鉄(FeO)からなる微小な粒子が多
く含まれている。
The slag glass produced from refuse incineration ash basically contains many fine particles of iron oxide (FeO) inside the produced glass because of its melting in a reduced state.

【0012】このようなものを加熱すると、高温の状態
では2FeO→2Fe+Oの反応が促進され(Feは
更に高温になるとガラス中に溶け込んでしまう)、ガラ
ス内部の微小な粒子の周囲に酸素ガスからなる気泡が多
く形成される。
When such a material is heated, the reaction of 2FeO → 2Fe + O 2 is promoted in a high temperature state (Fe dissolves in the glass at a higher temperature), and oxygen gas is surrounded by minute particles inside the glass. Many bubbles are formed.

【0013】スラグガラスは、850℃以上の高温状態
では軟化が始まり、温度の上昇に伴って粘度は急速に低
下するため、これらの気泡の大きさはガラスの粘度の低
下に伴って急速に増大する。950〜1050℃の温度
域に達すると、ガラスの粘度が急激に低下するので、気
泡が拡大して連続した泡(空間)となる。
The slag glass begins to soften at a high temperature of 850 ° C. or higher and its viscosity rapidly decreases with increasing temperature. Therefore, the size of these bubbles rapidly increases with decreasing glass viscosity. To do. When it reaches the temperature range of 950 to 1050 ° C., the viscosity of the glass sharply decreases, so that the bubbles expand and become continuous bubbles (space).

【0014】また、このような高温の条件下では、混合
された粘土は数100℃で脱水反応によってメタカオリ
ンを形成するが、更に高温条件下ではスラグガラス相と
反応して珪灰石(CaSiO)や準長石(CaAlS
)或は灰長石(CaAlSi)を形成
する。
Under such high temperature conditions, the mixed clay forms metakaolin by dehydration reaction at several 100 ° C., but under higher temperature conditions, it reacts with the slag glass phase and wollastonite (CaSiO 3 ). And quasi-feldspar (CaAlS
i 2 O 7 ) or anorthite (CaAl 2 Si 2 O 8 ) is formed.

【0015】これらは、連続した気泡の壁面を形成し、
更に3次元的なネットワーク構造を形成するが、これら
の骨格が最終製品の強度を保ち、製品に機能を付加して
いる。
These form the wall surface of continuous bubbles,
Further, it forms a three-dimensional network structure, but these skeletons maintain the strength of the final product and add functions to the product.

【0016】そして、この段階にいたって、連続した泡
が等しい粒径分布で存在する発泡材が形成される。
Then, up to this stage, a foam material in which continuous bubbles are present with an equal particle size distribution is formed.

【0017】このようなことから、発泡反応にはスラグ
ガラスの組成が大きく影響することとなるが、前述の如
く、スラグガラスの組成はゴミ焼却灰、即ち、焼却され
た汚泥や都市ゴミの組成により大きく異なるため、従来
においては、発泡量の安定した発泡材を得ることができ
なかった。
From the above, the composition of the slag glass has a great influence on the foaming reaction, but as described above, the composition of the slag glass is the composition of waste incineration ash, that is, the composition of incinerated sludge and municipal waste. However, in the past, it was not possible to obtain a foam material with a stable foaming amount.

【0018】これに対して、本発明に従って、炭酸ナト
リウム(Na CO )、実用的にはソーダ灰を配合す
ることにより、発泡量を著しく増加させて、発泡量を安
定させることができる。
In contrast, according to the present invention, sodium carbonate
By adding strontium (Na 2 CO 3 ), practically soda ash, it is possible to significantly increase the foaming amount and stabilize the foaming amount.

【0019】即ち、例えば、ソーダ灰は発泡原料中のナ
トリウム成分の増加を促進し、高温条件下でのスラグガ
ラスの粘度を大きく低下させることができ、800℃以
上の一定の温度において、ソーダ灰無添加のものと比較
するとガラスの軟化を大きく進行させることができる。
このために、800℃以上の焼成の過程で発生した気泡
は、ガラス相の軟化に伴い、900℃付近で急激な拡大
を生じて最終的には単独気泡がつながった連続気泡の集
合体となり、高発泡量の発泡材が形成される。
That is, for example, soda ash can promote the increase of the sodium component in the foaming raw material and can greatly reduce the viscosity of the slag glass under high temperature conditions. Compared with the additive-free one, the softening of the glass can be greatly promoted.
For this reason, the bubbles generated in the process of firing at 800 ° C. or higher rapidly expand at around 900 ° C. with the softening of the glass phase, and finally become an aggregate of continuous bubbles in which individual bubbles are connected, A foam material having a high foaming amount is formed.

【0020】炭酸ナトリウムはスラグガラスの粉砕物に
対して0.5〜10.0重量%、好ましくは3.0〜1
0.0重量%、より好ましくは3.0〜5.0重量%と
なるように、スラグガラスの粉砕物に対する粘土との合
計割合で15.0〜30.0重量%となるように添加す
る。
Sodium carbonate is 0.5 to 10.0% by weight, preferably 3.0 to 1 based on the slag glass pulverized product.
0.0 wt%, more preferably 3.0 to 5.0 wt%, so that the total ratio of clay to crushed slag glass is 15.0 to 30.0 wt%
It

【0021】また、焼成は、最高温度950〜1050
℃で行うのが好ましい。
The maximum temperature for firing is 950 to 1050.
It is preferable to carry out at ° C.

【0022】[0022]

【発明の実施の形態】以下に本発明の実施の形態を、本
発明の発泡材の製造手順に従って、詳細に説明するが、
以下の製造方法は本発明の発泡材の製造方法の一例であ
って、本発明の発泡材は、何ら以下の製造方法により製
造されたものに限定されるものではない。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, embodiments of the present invention will be described in detail in accordance with the procedure for producing a foam material of the present invention.
The following manufacturing method is an example of the method for manufacturing the foamed material of the present invention, and the foamed material of the present invention is not limited to that manufactured by the following manufacturing method.

【0023】本発明の発泡材を製造するには、まず、ス
ラグガラスを粉砕し、スラグガラスの粉砕物(以下、単
に「スラグガラス」と称す場合がある。)と粘土とを混
合する。
To produce the foamed material of the present invention, first, slag glass is crushed, and a crushed slag glass material (hereinafter sometimes simply referred to as "slag glass") is mixed with clay.

【0024】本発明において用いるスラグガラスは、ゴ
ミ焼却灰の還元溶融で製造されたものであり、このスラ
グガラスは粒径1.5mm以下に粉砕して使用される。
スラグガラスの粉砕粒径が大き過ぎると混合作業性が悪
く、発泡原料の均一混合物を得ることが困難となるが、
スラグガラスの粒径が過度に小さいと発泡性が悪くな
る。一般に、原料スラグガラスの粒径範囲は、74〜1
500μm、特に250〜1500μmであることが好
ましい。
The slag glass used in the present invention is produced by reduction melting of refuse incineration ash, and this slag glass is crushed to a particle size of 1.5 mm or less before use.
If the crushed particle size of the slag glass is too large, the mixing workability is poor and it becomes difficult to obtain a uniform mixture of foaming raw materials.
If the particle size of the slag glass is too small, the foamability will deteriorate. Generally, the particle size range of the raw slag glass is 74-1.
It is preferably 500 μm, and particularly preferably 250 to 1500 μm.

【0025】スラグガラスと混合する粘土には特に制限
はない。即ち、本発明において、使用する粘土の組成や
品質は、発泡性に殆ど影響しないため、どのような粘土
であっても同様の条件で使用することができる。
The clay mixed with the slag glass is not particularly limited. That is, in the present invention, the composition and quality of the clay used has almost no influence on the foamability, so that any clay can be used under the same conditions.

【0026】粘土の混合割合は、後述の炭酸ナトリウム
と粘土との合計の重量がスラグガラスに対して15.0
〜30.0重量%となるような量とする。粘土の割合が
上記範囲より少いと、発泡材に必要な強度を得ることが
できず、多いと発泡量の大きな発泡材は得られない。
The mixing ratio of clay is such that the total weight of the below-mentioned sodium carbonate and clay is 15.0 with respect to the slag glass.
30.0 shall be the amount such that the weight%. When the proportion of clay is less than the above range, the strength required for the foam material cannot be obtained, and when it is large, a foam material having a large foaming amount cannot be obtained.

【0027】次いで、スラグガラスと粘土との混合物に
炭酸ナトリウムを添加して、十分に均一に撹拌混合す
る。
Then, in a mixture of slag glass and clay
Add sodium carbonate and stir to mix evenly.

【0028】この炭酸ナトリウムの添加量は、多過ぎる
と焼成後に発泡材の周囲に炭酸ナトリウムの析出を生
じ、また、相対的に粘土添加量を減らすこととなり発泡
材に必要な強度を得ることが困難となる。逆に、炭酸ナ
トリウムの添加量が少ないと、発泡性の向上効果が得ら
れない。従って、炭酸ナトリウムはスラグガラスに対し
て0.5〜10.0重量%、好ましくは3.0〜10.
0重量%、より好ましくは3.0〜5.0重量%の範囲
で添加する。
If the amount of sodium carbonate added is too large, precipitation of sodium carbonate will occur around the foam material after firing, and the amount of clay added will be relatively reduced, so that the strength required for the foam material can be obtained. It will be difficult. On the contrary, if the addition amount of sodium carbonate is small, the effect of improving the foamability cannot be obtained. Therefore, sodium carbonate is 0.5 to 10.0% by weight, preferably 3.0 to 10.
0 wt%, more preferably added in a range of 3.0 to 5.0 wt%.

【0029】なお、本発明では、スラグガラスの種類即
ち発泡性の良否にかかわらず、一律の原料配合で同等の
発泡量を得ることができることが特徴であり、従って、
上記ソーダ灰の添加量は用いるスラグガラスの種類にか
かわらず、ほぼ一定とすることができる。
The present invention is characterized in that the same amount of foaming can be obtained by uniformly mixing the raw materials regardless of the type of slag glass, that is, the foamability.
The addition amount of the soda ash can be made substantially constant regardless of the type of slag glass used.

【0030】スラグガラス、粘土及びソーダ灰等の炭酸
ナトリウムを混合した後は、これに水を添加して混練す
る。この水の添加量は、一般に、スラグガラス、粘土及
炭酸ナトリウムの混合物の重量に対して10.0〜2
0.0重量%程度とされる。
Carbonic acid such as slag glass, clay and soda ash
After mixing sodium , water is added to this and kneading is performed. The amount of water added is generally 10.0-2 based on the weight of the mixture of slag glass, clay and sodium carbonate.
It is set to about 0.0% by weight.

【0031】次いで、この混練物を適当な大きさの型枠
に打ち込んで成形した後、焼成炉に入れて焼成する。こ
の成形に当り、型枠の種類や材質、形状、成形時の圧力
等は発泡性には大きく影響しないため、任意の条件を採
用することができる。また、焼成条件としては、昇温速
度はガラスの軟化を進行させ、同時に起こる発泡を促進
させる観点から、遅い方が好ましく、用いたスラグガラ
スの組成や生産効率を考慮して決定されるが、通常の場
合10〜20℃/分が好ましい。また、最高焼成温度は
950〜1050℃が好ましい。この温度が950℃未
満では十分に発泡が進行せず、1050℃を超えると高
温酸化が起こり褐色に変化することと、発泡材自身の軟
化が始まる。また、焼成後の冷却割れを防止するために
急冷却とならないように降温速度5〜50℃/分程度で
焼成後の冷却を行うのが好ましい。なお、使用する焼成
炉は、上記のような焼成条件での焼成が可能なものであ
れば良く、その型式には特に制限はない。また、加熱方
式も電気、ガスのいずれでも良い。
Next, the kneaded product is cast into a mold of an appropriate size to be molded, and then placed in a baking furnace and baked. In this molding, the type and material of the mold, the shape, the pressure during molding, etc. do not significantly affect the foamability, so any conditions can be adopted. Further, as the firing conditions, the heating rate is preferably slower from the viewpoint of promoting softening of the glass and promoting foaming that occurs at the same time, and is determined in consideration of the composition and production efficiency of the slag glass used, Usually, 10 to 20 ° C./minute is preferable. The maximum firing temperature is preferably 950 to 1050 ° C. If this temperature is lower than 950 ° C, foaming does not proceed sufficiently, and if it exceeds 1050 ° C, high-temperature oxidation occurs and the color changes to brown, and the foaming material itself begins to soften. Further, in order to prevent cooling cracks after firing, it is preferable to perform cooling after firing at a temperature lowering rate of about 5 to 50 ° C./min so that rapid cooling does not occur. The firing furnace used is not particularly limited as long as it can fire under the above firing conditions, and its type is not particularly limited. The heating method may be either electric or gas.

【0032】このようにして得られる本発明のスラグガ
ラスを用いた発泡材は、スラグガラスの種類にかかわら
ず、一般的にはスラグガラスに対して3.0〜5.0重
量%程度のソーダ灰の添加で、2.0〜3.9倍の発泡
倍率(焼成前の体積に対する焼成後の体積の割合)を安
定に得ることができ、このため、実用的な発泡材を容易
に工業生産することが可能となる。
The foam material using the slag glass of the present invention thus obtained is generally about 3.0 to 5.0% by weight of soda regardless of the type of slag glass. By adding ash, a foaming ratio of 2.0 to 3.9 times (ratio of the volume after firing to the volume before firing) can be stably obtained. Therefore, a practical foam material can be easily produced in industrial production. It becomes possible to do.

【0033】[0033]

【実施例】以下に実験例、実施例及び比較例を挙げて本
発明をより具体的に説明する。
EXAMPLES The present invention will be described more specifically below with reference to experimental examples, examples and comparative examples.

【0034】実験例1 発泡性が悪いと評価されているスラグガラスを用いて、
粒径と発泡性との関係を調べた。
Experimental Example 1 Using slag glass evaluated to have poor foamability,
The relationship between particle size and foamability was investigated.

【0035】まず、表1に示す粒度分布のスラグガラス
を用い、表1に示す割合でスラグガラスと粘土(木節粘
土)とを混合し、これに更にソーダ灰を混合し、得られ
た混合物に水を添加して混練した。この混練物を型に入
れて成形した後、焼成炉にて昇温速度10℃/分,高温
焼成温度950℃で15分保持,降温速度10℃/分で
焼成した。
First, slag glass having a particle size distribution shown in Table 1 was used, slag glass and clay (Kibushi clay) were mixed in the ratio shown in Table 1, and soda ash was further mixed with the mixture to obtain a mixture. Water was added to and kneaded. This kneaded product was put into a mold to be molded, and thereafter, it was baked at a temperature rising rate of 10 ° C./minute, a high temperature baking temperature of 950 ° C. for 15 minutes, and a temperature decreasing rate of 10 ° C./minute.

【0036】得られた発泡材について、発泡倍率を調
べ、結果を表1に示した。
The expansion ratio of the obtained foamed material was examined, and the results are shown in Table 1.

【0037】表1より、スラグガラスについては細粒部
分が多いと発泡性が悪いことから、発泡倍率の大きい発
泡材を得るためには、細粒部分を分級するのが好ましい
ことがわかる。
It can be seen from Table 1 that the slag glass has poor foamability when there are many fine particles, and therefore it is preferable to classify the fine particles in order to obtain a foam material having a large expansion ratio.

【0038】[0038]

【表1】 [Table 1]

【0039】実施例1〜7,比較例1 実験例1で用いたと同様のスラグガラス(粒径範囲50
0μm以下)及び粘土を用い、表2のソーダ灰添加率と
なるように、表2に示す配合で混合したこと以外は実験
例1と同様にして発泡材を製造し、その発泡倍率を調
べ、結果を表2に示した。
Examples 1 to 7, Comparative Example 1 Slag glass similar to that used in Experimental Example 1 (particle size range 50
0 μm or less) and clay were used to produce a foam material in the same manner as in Experimental Example 1 except that the soda ash addition rate shown in Table 2 was mixed, and the expansion ratio thereof was examined. The results are shown in Table 2.

【0040】表2より、ソーダ灰を添加することによ
り、発泡倍率が著しく高くなり、発泡量が安定すること
がわかる。また、発泡倍率の向上と、ソーダ灰の添加コ
ストを考慮した場合、ソーダ灰の添加量はスラグガラス
に対して3.0〜10.0重量%が好ましいことがわか
る。
From Table 2, it can be seen that the addition of soda ash markedly increases the expansion ratio and stabilizes the expansion amount. Further, when considering the improvement of the expansion ratio and the addition cost of soda ash, it is understood that the addition amount of soda ash is preferably 3.0 to 10.0% by weight with respect to the slag glass.

【0041】[0041]

【表2】 [Table 2]

【0042】実施例8,比較例2 異なる組成のスラグガラスA〜D(粒径範囲500μm
以下)を用い、ソーダ灰を添加した実施例においては下
記配合Iで混合し(スラグガラスに対するソーダ灰添加
率は3重量%)、ソーダ灰を添加しなかった比較例にお
いては下記配合IIで混合したこと以外は実験例1と同様
にして発泡材を製造した。
Example 8 and Comparative Example 2 Slag glasses A to D having different compositions (particle size range: 500 μm)
The following) was used to mix with soda ash in the following formula I (soda ash addition ratio to slag glass was 3% by weight), and in the comparative example without soda ash, the following formula II was mixed. A foam material was manufactured in the same manner as in Experimental Example 1 except that the above was performed.

【0043】 [0043]

【0044】得られた発泡材の発泡倍率を調べ、結果を
表3に示した。
The expansion ratio of the obtained foamed material was examined, and the results are shown in Table 3.

【0045】[0045]

【表3】 [Table 3]

【0046】表3より、ソーダ灰を添加することによ
り、すべてのスラグガラスに対して一律配合で、発泡倍
率を3倍〜4倍の範囲で安定させることができることが
わかる。
From Table 3, it can be seen that by adding soda ash, the expansion ratio can be stabilized in the range of 3 to 4 times with a uniform mixture for all slag glasses.

【0047】[0047]

【発明の効果】以上詳述した通り、本発明によれば、組
成や条件が大きく変化する汚泥や都市ゴミの焼却灰のス
ラグガラスから、均一な連続した気泡を持ち、発泡量の
安定した発泡材を得ることができ、これにより、廃棄物
の減容化、有効再利用を図ることができる。本発明の発
泡材は、気泡の大きさを容易に調節することによって、
防音効果を持つ吸音材として、或いは断熱材、その他、
住宅用又は産業用建材ないし構築材、充填材等として、
幅広い用途に極めて有用である。
As described in detail above, according to the present invention, the slag glass of incinerated ash of sludge or municipal waste whose composition and conditions are greatly changed has uniform continuous cells and a stable foaming amount. It is possible to obtain a material, which can reduce the volume and effectively reuse the waste. The foam material of the present invention, by easily adjusting the size of the cells,
As a sound absorbing material with soundproofing effect, heat insulating material, etc.
As residential or industrial building materials or construction materials, filling materials, etc.
Very useful for a wide range of applications.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 本田 哲 大阪府大阪市中央区道修町3丁目5番11 号 日本板硝子株式会社内 (56)参考文献 特開 平8−26844(JP,A) 特開 平6−87677(JP,A) 特開 平9−110549(JP,A) 特開 昭48−60114(JP,A) 特開 昭56−96767(JP,A) 作花 済夫 他2名編「ガラスハンド ブック」1981年 8月1日 株式会社朝 倉書店発行 第287.288頁 (58)調査した分野(Int.Cl.7,DB名) C04B 38/00 - 38/10 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Satoshi Honda 3-5-11 Doshomachi, Chuo-ku, Osaka-shi, Osaka, Japan Nippon Sheet Glass Co., Ltd. (56) Reference JP-A-8-26844 (JP, A) Kaihei 6-87677 (JP, A) JP 9-110549 (JP, A) JP 48-60114 (JP, A) JP 56-96767 (JP, A) Sakuo Sakuo and 2 others Volume "Glass Handbook" August 1, 1981, published by Asakura Shoten Co., Ltd. 287.288 pages (58) Fields investigated (Int.Cl. 7 , DB name) C04B 38/00-38/10

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ゴミ焼却灰をガラス化して得られるスラ
グガラスの粉砕物と粘土とを混合し、得られた混合物を
焼成して得られる発泡材において、 該混合物に炭酸ナトリウムを、スラグガラスの粉砕物に
対して0.5〜10.0重量%添加した発泡材であっ
て、 該スラグガラスの粉砕物に対する炭酸ナトリウムと粘土
との合計の割合が15.0〜30.0重量%である こと
を特徴とする焼却灰スラグガラスを用いた発泡材。
1. A slurry obtained by vitrifying refuse incineration ash.
The ground glass is mixed with clay and the resulting mixture is mixed.
In the foam material obtained by firing, Sodium carbonate to the mixtureFor slag glass crushed products
On the other hand, it is a foam material added with 0.5-10.0% by weight.
hand, Sodium carbonate and clay for crushed slag glass
And the total ratio is 15.0 to 30.0% by weight. thing
A foam material using incinerated ash slag glass.
【請求項2】 請求項1において、最高温度950〜1
050℃で焼成することを特徴とする焼却灰スラグガラ
スを用いた発泡材。
2. The method of claim 1] Oite to claim 1, the maximum temperature 950-1
A foam material using incinerated ash slag glass, which is fired at 050 ° C.
【請求項3】 請求項1又は2において、焼成前体積に
対する焼成後体積で表される発泡倍率が2倍以上である
ことを特徴とする焼却灰スラグガラスを用いた発泡材。
3. The method of claim 1 or 2, foam with ash slag glass, characterized in that the expansion ratio represented by the fired volume to the pre-firing volume is more than 2 times.
JP36333997A 1997-12-16 1997-12-16 Foam using incinerated ash slag glass Expired - Lifetime JP3440293B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
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JP3440293B2 true JP3440293B2 (en) 2003-08-25

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Country Link
JP (1) JP3440293B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2825512A1 (en) * 2012-03-13 2015-01-21 Joris Laarman Studio B.V. Ceramic foam
CN105060751B (en) * 2015-07-22 2017-04-26 中钢集团马鞍山矿山研究院有限公司 Preparation method for lightweight heat-preserving fireproof sheet material by utilizing hollow glass microspheres
CN110342956B (en) * 2019-08-21 2021-10-22 山西天合新材料科技有限公司 Low-cost ecological ceramic material with various sound absorption structures and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
作花 済夫 他2名編「ガラスハンドブック」1981年 8月1日 株式会社朝倉書店発行 第287.288頁

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