JPS6225620B2 - - Google Patents
Info
- Publication number
- JPS6225620B2 JPS6225620B2 JP56066300A JP6630081A JPS6225620B2 JP S6225620 B2 JPS6225620 B2 JP S6225620B2 JP 56066300 A JP56066300 A JP 56066300A JP 6630081 A JP6630081 A JP 6630081A JP S6225620 B2 JPS6225620 B2 JP S6225620B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- raw
- coal
- producing porous
- pellets
- 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
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B18/00—Use 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
- C04B18/04—Waste materials; Refuse
- C04B18/06—Combustion residues, e.g. purification products of smoke, fumes or exhaust gases
- C04B18/08—Flue dust, i.e. fly ash
- C04B18/085—Pelletizing
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/91—Use of waste materials as fillers for mortars or concrete
Landscapes
- 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)
- Processing Of Solid Wastes (AREA)
Description
本発明は、フライアツシユを主原料とする人工
軽量骨材の製造法に関し、殊にフライアツシユに
対する配合材の粒度構成及び配合比を工夫するこ
とにより軽量且つ吸水性に優れた軽量骨材を製造
できるようにしたものである。
石炭焚きボイラー等から発生するフライアツシ
ユの利用技術として、該フライアツシユを主原料
とする造粒物を焼結して軽量骨材とする技術があ
り、本発明者等は先にその改良法として特願昭55
−112806、特願昭55−175020等を提案している。
即ちフライアツシユには、元来若干の未燃炭素
が含まれているが、必要により可燃性炭素材(石
炭やコークスの微砕物)を加え、水をバインダー
として混練造粒し、生ペレツトとした後、これを
移動火格子上に装入して搬送しながら乾燥・予
熱・着火・焼結・保熱及び冷却を順次行ない人工
軽量骨材とするものである。このようにして得た
軽量骨材(軽量骨材A)は、見掛比重が1.3〜1.5
g/cm3と比較的小さいから建築用軽量骨材として
の有効利用が期待されている。しかしながら膨張
けつ岩を回点転式キルンにより焼成して得られる
汎用の軽量骨材(軽量骨材B:見掛比重1.2〜1.3
g/cm3)に比べると比重が若干大きく、建築用軽
量骨材としての用途を拡大して行く為には軽量骨
材Bに匹敵し得る様な軽量化を達成する必要があ
る。
一方軽量骨材Aの吸水率(24時間浸漬後の吸水
率)は10〜18%であり、軽量骨材Bの吸水率が3
〜6%であるのに比べるとはるかに大きな値を示
しており、温室等における濃園芸用調湿材や施水
材、施肥材等の用途に対しては軽量骨材Bよりも
むしろ適している。しかし、このような用途への
適応性を高めるうえでは吸水率を更に大きくする
ことが望まれる。
以上のように軽量骨材Aは通常の用途では一応
要求品質を満足しているが、一層軽量化し且つ吸
水率を向上させることが強く要望されており、こ
れらの点を満足できればフライアツシユの用途は
更に拡大するものと期待される。殊に石油事情の
悪化に伴なつて石炭焚きは今後益々増加すること
が明白であり、それにつれて激増すると考えられ
るフライアツシユの有効利用分野を拡大しておく
ことは極めて重要なことである。
本発明は、この様な状況のもとで軽量骨材Aを
軽量化すると共に、吸水率を一層向上することが
できる様な製造法の確立を期して鋭意研究の結果
完成されたものであつて、その構成はフライアツ
シユを主原料とし水をバインダーとして混練し、
これを転動造粒してられる生ペレツトを移動火核
格子に載せて移送させつつ焼結する多孔性骨材の
製造方法において、前記生ペレツト原料に粒径1
mm以下の粒度分含有率が60〜90重量%である次の
各添加物群
石炭灰:5〜30重量%
粗粉炭:3〜10重量%
有機物含有固形物の磨砕物:1〜30重量%
から選択される1種以上を全原料の無水重量基準
で夫々配合して生ペレツトを転動造粒する点に要
旨を有する。
本発明で用いるフライアツシユは、ボイラー等
で燃焼させる原料微粉炭の品質等により多少の変
動はあるが、325メツシユ以下の粒度のものが約
70重量%(以下単に%ということがある)を占め
る微粉状物であり、又生ペレツトの自燃性を高め
る目的で必要により添加されることのある可燃性
炭素材としては、74μm以下の粒度のものが約70
%を占める微粉炭が好まれる。
本発明では、基本的には上記の成分を主体とす
るのであるが、これに比較的大粒度の石炭灰、粗
粉炭、有機物含有固形物よりなる群から選択され
る1種以上の添加物を所定範囲で添加した組成の
造粒物を焼結することにより、軽量で且つ吸水率
の良好な骨材を得ることができた。
上記3種の添加物は、いずれも1mm以下の粒度
分含有率が60〜90%のものでなければならず、か
かる粒度構成のものを使用することによつて、焼
結ペレツトの気孔率を高め、軽量化、高吸水率化
の両目的を達成することができる。即ち粒径1mm
を越えるものが多すぎると結合力が乏しくなつ
て、造粒することが困難になり、たとえ造粒し得
たとしても焼結時に崩壊し易く歩留りが低下す
る。尚含有率が60%未満であるとこれら粒体の間
に微細なフライアツシユがかみこまれて気孔率を
増大させることができなくなる。
次に上記3種の添加物の個々について配合率設
定の理由等を説明する。
まず石炭灰を添加する場合の配合率は全原料の
無水重量基準(無水生ペレツト基準、以下同じ)
で5〜30%の範囲となる様に選択しなければなら
ず、配合率が30%を越えると石炭灰が粗大粒子で
ある為に結合力が乏しくなつて造粒することが困
難になり、一方5%未満では気孔率向上効果が不
十分で軽量化及び吸水率向上の効果が現れない。
石炭灰の例としては、石炭焚きボイラー等から排
出されるボトムアツシユを前記粒度範囲に粉砕し
たもの或はボイラーのエアヒータやエコノマイザ
近辺から排出されるシンダー灰等が挙げられる。
添加物として石炭灰のみを使用する場合は必要に
応じて微粉炭を配合し、生ペレツトに含まれる内
装炭材量が4〜6%となるように調整することが
望まれる。
次に粗粉炭を添加する場合の配合率は、生ペレ
ツトに対して3〜10%の範囲から選択しなければ
ならず、配合率が10%を越えると石炭灰の場合と
同様、生ペレツトを造粒することが困難になると
共に焼結物の強度が弱くなり、一方3%未満では
焼結物の軽量化、吸水率の向上をはかることがで
きない。粗粉炭の例としては石炭を粗粉砕したも
のが挙げられる。尚粗粉炭は多量の可燃性炭素を
含んでおり、それ自身で生ペレツトに自燃性を与
える作用があるから、微粉炭の併用は必要でない
が、何れにしても生ペレツトに含まれる内装炭材
量が3〜10%となるように配合率を調整するのが
よい。
又有機物含有固形物を添加する場合の配合率は
生ペレツトに対して1〜30%の範囲から選択しな
ければならず配合率が30%を越えると、同様に、
生ペレツトを造粒することが困難になり、一方1
%未満では焼結物の軽量化、吸水率の向上をはか
ることができない。有機物含有固形物の磨砕物の
例としては、パルプ屑、おが屑、木屑、プラスチ
ツク片等を前記粒度に磨砕したものが挙げられ
る。尚有機物含有固物を使用する場合、その可燃
炭素含有率によつては生ペレツトに自燃性を与え
る為に適量の微粉炭を併用する必要があるが、何
れにしても生ペレツトに含まれる内装炭材量が2
〜6%となるように調整することが望まれる。
上記3種の添加物は夫々単独でフライアツシユ
基本組成に配合し得るほか、これらを適当に組み
合わせて配合することもでき、むしろ組み合わせ
によつて本発明の効果を更に高めることができ
る。
本発明は以上のように構成されており、建築用
等の用途に十分適応できる強度を保ちながら、軽
量で且つ吸水性に優れた軽量骨材を提供し得るこ
とになつたもので、建築用以外の用途(前述の様
な園芸裁培用軽量骨材等)に対しても巾広く利用
可能にした意義は頻る大きい。
以下本発明の実施例を説明する。
実施例 1
未燃炭素3%を含むフライアツシユ(粒径44μ
m以下のもの70%含有)に粉砕したボトムアツシ
ユ(粒径1mm以下のもの60%含有)を10%混合
し、該混合物に炭素量が5%となるように通常粒
度の微粉炭を添加し、水を16%加えて約12mmφの
ペレツトに造粒する。尚造粒には傾斜皿型造粒機
を使用した(以下同じ)。該ペレツトをドワイト
ロイド式焼結機に約300mmの厚さとなる様に装入
し16.000Kcal/m2・分の熱量を2分間与えて着火
した後、下方から吸引しつつ自燃により焼結させ
て結ペレツトを得た。
実施例 2
実施例1で用いたのと同様のフライアツシユ
に、シンダー灰(粒径74μ以下のものを30%含有
し、且つ1mm以下のものを80%含有する)を20%
混合し、そこへ内装炭素量を5%となるように微
粉炭を添加混合し、水を約17%添加し約12mmφの
ペレツトに造粒した後、実施例1と同様にして焼
結ペレツトを得た。
実施例 3
実施例1で用いたのと同様のフライアツシユ
に、粗粉砕した石炭(粒径1mm以下のものを70%
含有する)を10%混合し、水を約16%添加して約
12mmφのペレツトに造粒した。該ペレツトをドワ
イトロイド式焼結機に約250mmの厚さとなる様に
装入し、5.000Kcal/m2・分の熱量を2分間与え
て予熱し、16.000Kcal/m2・分の熱量を1分間与
えて着火した後、下方から吸引しつつ自燃により
焼結させて焼結ペレツトを得た。
実施例 4
実施例1で用いたのと同様のフライアツシユに
炭素量が4%となるように微粉炭を加え、更に乾
燥・磨砕したおが屑(粒径1mm以下のものを70%
含有する)を10%添加し水を約20%加えて約12mm
φのペレツトに造粒後、実施例3と同様にして焼
結ペレツトを得た。
比較例
実施例1で用いたのと同様のフライアツシユに
微粉炭(粒径74μm以下のものを67%含有する)
を加え炭素量5%としたものに、水を17%添加し
て約12mmφの生ペレツトを造粒しこれを実施例1
と同様にして焼結させて焼結ペレツトを得た。
上記実施例及び比較例で得た各焼結ペレツトの
見掛比重、吸水率及び圧潰強度を第1表に一括し
て示す。
The present invention relates to a method for producing artificial lightweight aggregate using fly ash as the main raw material, and in particular, by devising the particle size structure and blending ratio of materials mixed with fly ash, it is possible to produce lightweight aggregate with excellent water absorption. This is what I did. As a technology for utilizing fly ash generated from coal-fired boilers, etc., there is a technology to sinter granules made from fly ash as the main raw material to produce lightweight aggregate, and the present inventors have previously filed a patent application for an improved method. Showa 55
-112806, patent application No. 175020, etc. In other words, fly ash originally contains some unburned carbon, but if necessary, combustible carbon material (pulverized coal or coke) is added, water is used as a binder, and the mixture is kneaded and granulated to form raw pellets. This is then charged onto a moving grate and transported while drying, preheating, igniting, sintering, retaining heat, and cooling in order to produce an artificial lightweight aggregate. The lightweight aggregate thus obtained (lightweight aggregate A) has an apparent specific gravity of 1.3 to 1.5.
Since it is relatively small at g/ cm3 , it is expected to be used effectively as a lightweight aggregate for construction. However, general-purpose lightweight aggregate obtained by firing expanded rock in a rotary kiln (lightweight aggregate B: apparent specific gravity 1.2 to 1.3
g/cm 3 ), and in order to expand its use as a lightweight aggregate for construction, it is necessary to achieve a weight reduction comparable to that of lightweight aggregate B. On the other hand, the water absorption rate of lightweight aggregate A (water absorption rate after 24-hour immersion) is 10 to 18%, and the water absorption rate of lightweight aggregate B is 3.
It shows a much larger value compared to ~6%, and is more suitable than lightweight aggregate B for applications such as a humidity control material for concentrated horticulture, a watering material, and a fertilizing material in greenhouses and the like. However, in order to improve the adaptability to such uses, it is desirable to further increase the water absorption rate. As mentioned above, lightweight aggregate A satisfies the required quality for normal use, but there is a strong demand for further weight reduction and improved water absorption.If these points can be satisfied, fly aggregate use will be possible. It is expected that it will further expand. In particular, as the oil situation worsens, it is clear that coal-fired combustion will increase even more in the future, and it is extremely important to expand the fields in which fly ash can be effectively used, as this is expected to increase dramatically. Under these circumstances, the present invention was completed as a result of intensive research with the aim of establishing a manufacturing method that can reduce the weight of lightweight aggregate A and further improve its water absorption rate. Its composition is made by kneading fly assemblage as the main raw material and water as a binder.
In a method for producing porous aggregate, in which raw pellets obtained by rolling granulation are placed on a moving nuclear grate and sintered while being transferred, the raw pellet raw material has a particle size of 1.
Each of the following additive groups whose particle size content is 60 to 90% by weight: Coal ash: 5 to 30% by weight Coarse pulverized coal: 3 to 10% by weight Ground solids containing organic matter: 1 to 30% by weight The gist is that raw pellets are granulated by rolling by blending one or more selected from the following on the basis of the dry weight of all raw materials. The fly ash used in the present invention may vary slightly depending on the quality of the raw material pulverized coal burned in the boiler, etc., but the particle size of the fly ash used in the present invention is approximately 325 mesh or less.
The combustible carbon material is a fine powder that accounts for 70% by weight (hereinafter simply referred to as %), and may be added as necessary to improve the self-combustibility of raw pellets, with a particle size of 74 μm or less. About 70 things
% of pulverized coal is preferred. In the present invention, the above ingredients are basically the main ingredients, but one or more additives selected from the group consisting of relatively large-grained coal ash, coarse pulverized coal, and organic matter-containing solids are added to these ingredients. By sintering the granules with a composition added in a predetermined range, it was possible to obtain lightweight aggregate with good water absorption. All of the above three types of additives must have a particle size content of 60 to 90% of 1 mm or less, and by using particles with such a particle size composition, the porosity of the sintered pellets can be reduced. It is possible to achieve both the objectives of heightening, weight reduction, and high water absorption. i.e. particle size 1mm
If the amount exceeds too much, the bonding force will be poor and it will be difficult to granulate, and even if granules can be granulated, they will easily collapse during sintering and the yield will decrease. If the content is less than 60%, fine fly ash will be trapped between these particles, making it impossible to increase the porosity. Next, the reasons for setting the blending ratios for each of the above three types of additives will be explained. First, when adding coal ash, the blending ratio is based on the dry weight of all raw materials (based on anhydrous raw pellets, the same applies hereinafter).
If the blending ratio exceeds 30%, the coal ash will be coarse particles and will have poor binding strength, making it difficult to granulate. On the other hand, if it is less than 5%, the effect of improving porosity is insufficient and the effect of reducing weight and improving water absorption rate does not appear.
Examples of coal ash include bottom ash discharged from a coal-fired boiler etc. which is pulverized into the particle size range described above, and cinder ash discharged from the vicinity of the air heater or economizer of the boiler.
When only coal ash is used as an additive, it is desirable to mix pulverized coal as necessary to adjust the amount of internal carbon material contained in the raw pellets to 4 to 6%. Next, when adding coarse powder coal, the blending ratio must be selected from the range of 3 to 10% based on the raw pellets, and if the blending ratio exceeds 10%, the raw pellets will be added as is the case with coal ash. It becomes difficult to granulate the sintered product and the strength of the sintered product becomes weaker. On the other hand, if the content is less than 3%, it is impossible to reduce the weight of the sintered product or improve its water absorption rate. Examples of coarse pulverized coal include coarsely pulverized coal. Coarse pulverized coal contains a large amount of combustible carbon and has the effect of giving self-combustibility to the raw pellets, so it is not necessary to use pulverized coal together, but in any case, the inner carbon material contained in the raw pellets It is best to adjust the blending ratio so that the amount is 3 to 10%. In addition, when adding organic matter-containing solids, the blending ratio must be selected from the range of 1 to 30% based on the raw pellets, and if the blending ratio exceeds 30%, similarly,
It becomes difficult to granulate raw pellets, while 1
If it is less than %, it is not possible to reduce the weight of the sintered product or improve its water absorption rate. Examples of the ground material containing organic matter include pulp waste, sawdust, wood chips, plastic pieces, etc., ground to the above-mentioned particle size. When using solids containing organic matter, depending on the combustible carbon content, it is necessary to use an appropriate amount of pulverized coal in order to give the raw pellets self-combustibility, but in any case, the interior content of the raw pellets The amount of carbon material is 2
It is desirable to adjust it to ~6%. The three types of additives mentioned above can be incorporated into the fly ash basic composition individually, or they can be incorporated in an appropriate combination.In fact, the effects of the present invention can be further enhanced by the combination. The present invention is configured as described above, and it has become possible to provide a lightweight aggregate that is lightweight and has excellent water absorbency while maintaining sufficient strength for use in construction, etc. It is of great significance to make it widely available for other uses (such as lightweight aggregate for horticultural culture as mentioned above). Examples of the present invention will be described below. Example 1 Fly ash containing 3% unburned carbon (particle size 44μ)
Mix 10% of pulverized bottom ash (containing 60% of particles with a particle size of 1 mm or less) with 70% of particles with a particle size of 1 mm or less, and add pulverized coal of normal particle size to the mixture so that the carbon content is 5%. Add 16% water and granulate into pellets of approximately 12 mmφ. A tilted dish granulator was used for granulation (the same applies hereinafter). The pellets were charged into a Dwight Lloyd sintering machine to a thickness of approximately 300 mm, ignited by applying heat of 16,000 Kcal/m 2 ·min for 2 minutes, and then sintered by self-combustion while suctioning from below. A pellet was obtained. Example 2 In the same fly ash as used in Example 1, 20% cinder ash (containing 30% particles with a particle size of 74μ or less and 80% particles with a particle size of 1 mm or less) was added.
After mixing, pulverized coal was added and mixed so that the internal carbon content was 5%, and about 17% of water was added to form pellets of about 12 mmφ, and then sintered pellets were made in the same manner as in Example 1. Obtained. Example 3 Coarsely crushed coal (70% of which had a particle size of 1 mm or less) was placed in a fly ash similar to that used in Example 1.
Mix 10% of (containing) and add about 16% of water to make approx.
It was granulated into pellets with a diameter of 12 mm. The pellets were charged into a Dwight Lloyd type sintering machine to a thickness of about 250 mm, preheated by applying a heat amount of 5.000 Kcal/ m2・min for 2 minutes, and then heated to a heat value of 16.000 Kcal/ m2・min. After being ignited for a few minutes, the pellets were sintered by self-combustion while suctioning from below to obtain sintered pellets. Example 4 Pulverized coal was added to the same fly ash as used in Example 1 so that the carbon content was 4%, and dried and ground sawdust (70% of which had a particle size of 1 mm or less) was added.
Add 10% of (containing) and add about 20% of water to make about 12mm.
After granulation into pellets of φ, sintered pellets were obtained in the same manner as in Example 3. Comparative example Pulverized coal (containing 67% particles with a particle size of 74 μm or less) was added to the same fly ash as used in Example 1.
was added to make the carbon content 5%, and 17% water was added to make raw pellets of approximately 12mmφ, which were prepared in Example 1.
Sintered pellets were obtained in the same manner as above. Table 1 shows the apparent specific gravity, water absorption rate, and crushing strength of each sintered pellet obtained in the above examples and comparative examples.
【表】
であればよい。
[Table] is fine.
Claims (1)
シユを主原料とし水をバインダーとして混練し、
これを転動造粒して得られる生ペレツトを移動火
格子に載せて移送させつつ焼結する多孔性骨材の
製造方法において、前記生ペレツト原料に、粒径
1mm以下の粒度分含有率が60〜90重量%である下
記の各添加物群から選択される1種以上を全原料
の無水重量基準で夫々配合して転動造粒すること
を特徴とする多孔性骨材の製造方法。 石炭灰:5〜30重量% 粗粉炭:3〜10重量% 有機物含有固形物の磨砕物:1〜30重量% 2 特許請求の範囲第1項において、石炭灰を配
合して造粒した生ペレツトが可燃性炭素分を4〜
6重量%含有するものである多孔性骨材の製造方
法。 3 特許請求の範囲第1項において、粗粉炭を配
合して造粒した生ペレツトが可燃性炭素分を3〜
10重量%含有するものである多孔性骨材の製造方
法。 4 特許請求の範囲第1項において、有機物含有
固形物の磨砕物を配合して造粒した生ペレツトが
可燃性炭素分を2〜6重量%含有するものである
多孔性骨材の製造方法。[Claims] 1. Kneading fly ash generated from a coal-fired boiler etc. as the main raw material and water as a binder,
In a method for producing porous aggregate in which raw pellets obtained by rolling granulation are sintered while being transferred on a moving grate, the raw pellet raw material contains a particle size fraction of 1 mm or less. A method for producing porous aggregates, which comprises blending 60 to 90% by weight of one or more selected from the following additive groups based on the dry weight of the total raw materials and rolling granulation. Coal ash: 5 to 30% by weight Coarse pulverized coal: 3 to 10% by weight Ground material of organic matter-containing solids: 1 to 30% by weight 2. In claim 1, raw pellets granulated by blending coal ash. The combustible carbon content is 4~
A method for producing porous aggregate containing 6% by weight. 3 In claim 1, raw pellets granulated with coarse powdered coal have a combustible carbon content of 3 to 3.
A method for producing porous aggregate containing 10% by weight. 4. The method for producing porous aggregate according to claim 1, wherein the raw pellets granulated by blending the ground material containing organic matter contain 2 to 6% by weight of combustible carbon.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6630081A JPS57183355A (en) | 1981-04-30 | 1981-04-30 | Manufacture of porous aggregate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6630081A JPS57183355A (en) | 1981-04-30 | 1981-04-30 | Manufacture of porous aggregate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57183355A JPS57183355A (en) | 1982-11-11 |
| JPS6225620B2 true JPS6225620B2 (en) | 1987-06-04 |
Family
ID=13311818
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6630081A Granted JPS57183355A (en) | 1981-04-30 | 1981-04-30 | Manufacture of porous aggregate |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57183355A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0717417B2 (en) * | 1986-04-25 | 1995-03-01 | 工業技術院長 | Method for manufacturing lightweight aggregate for concrete |
| GB0320140D0 (en) * | 2003-08-28 | 2003-10-01 | Peskett Anthony | Synthetic stone aggregate |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5669262U (en) * | 1979-10-26 | 1981-06-08 |
-
1981
- 1981-04-30 JP JP6630081A patent/JPS57183355A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57183355A (en) | 1982-11-11 |
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