JP2000247701A - Production of artificial lightweight aggregate and artificial aggregate - Google Patents
Production of artificial lightweight aggregate and artificial aggregateInfo
- Publication number
- JP2000247701A JP2000247701A JP5341999A JP5341999A JP2000247701A JP 2000247701 A JP2000247701 A JP 2000247701A JP 5341999 A JP5341999 A JP 5341999A JP 5341999 A JP5341999 A JP 5341999A JP 2000247701 A JP2000247701 A JP 2000247701A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- aggregate
- artificial lightweight
- lightweight aggregate
- ash
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000000203 mixture Substances 0.000 claims abstract description 21
- 239000010883 coal ash Substances 0.000 claims abstract description 20
- 239000002956 ash Substances 0.000 claims abstract description 18
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical group [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims abstract description 16
- 230000005484 gravity Effects 0.000 claims abstract description 16
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 15
- 239000004088 foaming agent Substances 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 15
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910010271 silicon carbide Inorganic materials 0.000 claims abstract description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 238000010521 absorption reaction Methods 0.000 claims abstract description 12
- 239000003575 carbonaceous material Substances 0.000 claims abstract description 10
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 239000011230 binding agent Substances 0.000 claims abstract description 7
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 5
- 239000011575 calcium Substances 0.000 claims abstract description 5
- 238000001035 drying Methods 0.000 claims abstract description 4
- 238000010304 firing Methods 0.000 claims description 16
- 238000004056 waste incineration Methods 0.000 claims description 4
- 239000002994 raw material Substances 0.000 abstract description 11
- 239000000047 product Substances 0.000 abstract description 8
- 238000010276 construction Methods 0.000 abstract description 3
- 238000007906 compression Methods 0.000 abstract description 2
- 230000006835 compression Effects 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract description 2
- 238000002156 mixing Methods 0.000 abstract description 2
- 239000012467 final product Substances 0.000 abstract 1
- 239000010881 fly ash Substances 0.000 description 15
- 239000008188 pellet Substances 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 10
- 229910052595 hematite Inorganic materials 0.000 description 10
- 239000011019 hematite Substances 0.000 description 10
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 10
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 239000000571 coke Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 239000000440 bentonite Substances 0.000 description 8
- 229910000278 bentonite Inorganic materials 0.000 description 8
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 8
- 239000007789 gas Substances 0.000 description 6
- 239000000292 calcium oxide Substances 0.000 description 5
- 235000012255 calcium oxide Nutrition 0.000 description 5
- 238000005187 foaming Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000003245 coal Substances 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 239000000567 combustion gas Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 102100033007 Carbonic anhydrase 14 Human genes 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 101000867862 Homo sapiens Carbonic anhydrase 14 Proteins 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- LFYJSSARVMHQJB-QIXNEVBVSA-N bakuchiol Chemical compound CC(C)=CCC[C@@](C)(C=C)\C=C\C1=CC=C(O)C=C1 LFYJSSARVMHQJB-QIXNEVBVSA-N 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- -1 coke are added Chemical compound 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000012254 powdered material Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000013441 quality evaluation Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 238000004017 vitrification Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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
- C04B18/02—Agglomerated materials, e.g. artificial aggregates
- C04B18/027—Lightweight materials
-
- 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)
- Civil Engineering (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Processing Of Solid Wastes (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、ごみ焼却施設など
から発生するごみ焼却灰を主原料とする土木・建築用人
工軽量骨材とその製造する方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an artificial lightweight aggregate for civil engineering and construction mainly using refuse incineration ash generated from a refuse incineration facility or the like, and a method for producing the same.
【0002】[0002]
【従来の技術】ごみ焼却施設などから発生するごみ焼却
灰には、焼却残渣である主灰と排ガス中より捕集した飛
灰とがあり、そのほとんどが廃棄物として埋め立て処分
されている。飛灰には鉛、カドミウムなどの重金属類が
含まれているため、溶融固化、セメント固化、キレート
処理あるいは酸洗浄などの方法により重金属類の溶出防
止処理を施して無害化したあとに埋め立て処分してい
る。2. Description of the Related Art Waste incineration ash generated from waste incineration facilities includes main ash, which is incineration residue, and fly ash collected from exhaust gas, and most of them are landfilled as waste. Since fly ash contains heavy metals such as lead and cadmium, it is treated to prevent leaching of heavy metals by melt solidification, cement solidification, chelate treatment, or acid washing, and is rendered harmless. ing.
【0003】しかし、溶融固化法は処理コストが高く、
またそれ以外の方法は長期信頼性に欠けるという問題が
あり、加えて多くの自治体が最終処分場の確保と残余年
数の延長化に苦慮しているため、飛灰を廃棄物とせず再
資源として有効利用する技術の開発が期待されている。However, the melting and solidification method has a high processing cost,
Other methods have the problem of lack of long-term reliability.In addition, many municipalities are struggling to secure final disposal sites and extend the remaining years, so fly ash is not recycled as waste but as recycled. The development of technology for effective use is expected.
【0004】その方法の一つとして本発明者らは先に、
飛灰を主原料として粘結剤や珪砂、陶石および長石など
の組成制御剤、さらにはヘマタイト、炭化珪素などの発
泡剤、コークスなどの還元剤を添加し、ペレット化し、
得たペレットをロータリーキルンで焼成することによっ
て重金属溶出量の少ない土木・建築用人工軽量骨材の製
造方法を見出し、この技術を特開平10−287675
号に開示した。As one of the methods, the present inventors have previously described:
Using fly ash as a main raw material, a binder, a silica sand, a composition controlling agent such as pottery stone and feldspar, a foaming agent such as hematite and silicon carbide, and a reducing agent such as coke are added, and pelletized.
By firing the obtained pellets in a rotary kiln, a method for producing an artificial lightweight aggregate for civil engineering and construction with a small amount of heavy metal elution was found, and this technique was disclosed in JP-A-10-287675.
Issue.
【0005】この方法によれば、飛灰を人工軽量骨材と
して有効利用でき、かつ最終処分場の残余年数の延長に
も貢献できるが、飛灰の性状は焼却施設、設備、燃焼物
および運転状況などで大きく異なるため、用途に応じた
所望の骨材を製造するには添加剤による組成制御が必要
である。このような観点から、さらに本発明者らは組成
制御剤添加についての技術を特願平10−360909
に開示したが、より安価な組成制御剤による製造法につ
いての詳細な検討が必要であった。[0005] According to this method, fly ash can be effectively used as artificial lightweight aggregate and can contribute to the extension of the remaining years of the final disposal site. Since it varies greatly depending on the situation and the like, it is necessary to control the composition with additives in order to produce a desired aggregate according to the application. From such a viewpoint, the present inventors further describe a technique for adding a composition control agent to the present invention by Japanese Patent Application No. 10-360909.
However, a detailed study on a production method using a less expensive composition control agent was required.
【0006】[0006]
【発明が解決しようとする課題】ところで、このように
作製された人工軽量骨材は吸水性が高く、土木・建築材
料として必ずしも十分ではないとの指摘がある。そこで
本発明は、絶乾比重1.0〜1.5g/cm3、一軸圧
縮破壊荷重が30kgf以上で、かつ吸水率が5%以下
の人工軽量骨剤と、これを主原料として焼却灰てより安
価、かつ簡単に製造する方法の提供を目的とする。However, it has been pointed out that the thus produced artificial lightweight aggregate has high water absorption and is not always sufficient as a civil engineering / building material. Therefore, the present invention provides an artificial lightweight skeleton having a bone-dry specific gravity of 1.0 to 1.5 g / cm 3 , a uniaxial compression breaking load of 30 kgf or more, and a water absorption of 5% or less, and incineration ash using this as a main raw material. It is an object of the present invention to provide a cheaper and simpler manufacturing method.
【0007】[0007]
【課題を解決するための手段】本発明者らは上記焼却灰
の有効利用率を高め、絶乾比重が1.0〜1.5g/c
m3で、強度が高く、かつ吸水率が低い骨材を得るため
に鋭意検討した結果、骨材の組成制御剤としてある量の
石炭灰を添加すれば、上記課題を解決し得ることを見出
し本発明を完成するに至った。Means for Solving the Problems The present inventors have increased the effective utilization rate of the above incinerated ash, and have an absolute dry specific gravity of 1.0 to 1.5 g / c.
As a result of intensive studies to obtain an aggregate having a high strength and a low water absorption at m 3 , it was found that the above problem could be solved by adding a certain amount of coal ash as an agent for controlling the composition of the aggregate. The present invention has been completed.
【0008】すなわち上記目的を達成する本第1の発明
は、ごみ焼却灰に、粘結剤、発泡剤、還元剤と、さらに
組成制御剤として石炭灰とを混合し、得られた混合物を
粉砕し、該粉砕物に水を加えて成型し、該成型体を要す
れば乾燥し、次いで焼成して人工軽量骨材を得る方法に
おいて、最終的に得られる人工軽量骨材中のカルシウム
含有量が、酸化物換算で16重量%以下となるように組
成制御する人工軽量骨材の製造方法である。そして好ま
しくは、前記発泡剤として酸化鉄および/または炭化珪
素を用い、前記還元剤として炭材を用いる。That is, the first aspect of the present invention which achieves the above object is to mix a waste incineration ash with a binder, a foaming agent, a reducing agent and coal ash as a composition controlling agent, and pulverize the resulting mixture. Then, water is added to the pulverized material, and the molded body is dried, if necessary, and then fired to obtain an artificial lightweight aggregate. Is a method for producing an artificial lightweight aggregate in which the composition is controlled to be 16% by weight or less in terms of oxide. Preferably, iron oxide and / or silicon carbide is used as the foaming agent, and carbonaceous material is used as the reducing agent.
【0009】また本第2の発明は本第1の発明によって
得られる人工軽量骨材であり、絶乾比重が1.0〜1.
5g/cm3、一軸圧縮破壊荷重が30kgf以上、か
つ吸水率が5%以下である人工軽量骨材を特徴とするも
のである。The second invention is an artificial lightweight aggregate obtained by the first invention, and has an absolute dry specific gravity of 1.0 to 1.0.
It is characterized by an artificial lightweight aggregate having 5 g / cm 3 , a uniaxial compressive breaking load of 30 kgf or more, and a water absorption of 5% or less.
【0010】[0010]
【発明の実施の形態】以下、本発明の詳細およびその作
用についてさらに具体的に説明する。一般の人工軽量骨
材の原料である粘土や頁岩などの主成分は、シリカ、ア
ルミナ、カルシアなどであり、飛灰の成分もほぼ同様の
ものからなる。そして、人工軽量骨材に機械的強度を持
たせるためには焼成時にペレット内部を半溶融状態にさ
せてガラス化すればよく、また軽量化するためには内部
を溶融させ、適度な粘性低下と同時に揮発成分による気
泡を内部に捕捉すればよい。比重制御はこのような発泡
状態の調整によって行うことができる。BEST MODE FOR CARRYING OUT THE INVENTION The details of the present invention and its operation will be more specifically described below. The main components such as clay and shale, which are the raw materials of general artificial lightweight aggregate, are silica, alumina, calcia, and the like, and the components of fly ash are almost the same. Then, in order to impart mechanical strength to the artificial lightweight aggregate, the inside of the pellet may be made into a semi-molten state at the time of firing and vitrified, and in order to reduce the weight, the inside is melted, and a suitable viscosity reduction and At the same time, air bubbles due to volatile components may be captured inside. Specific gravity control can be performed by adjusting such a foaming state.
【0011】しかしながら、ごみ焼却施設などから発生
するごみ焼却灰は、焼却施設、燃焼物および運転状態な
どによって化学的・物理的性質が異なり、一般の人工軽
量骨材の原料である天然鉱物と比較してシリカやアルミ
ナなどの含有量が低いため、ペレット内部を半溶融状態
にしてガラス化し、機械的強度を持たせることが困難で
ある。However, incineration ash generated from refuse incineration facilities and the like has different chemical and physical properties depending on the incineration facilities, combustion products, operating conditions, and the like, and is incomparable with natural minerals that are raw materials for general artificial lightweight aggregates. Therefore, since the content of silica, alumina, and the like is low, it is difficult to vitrify the inside of the pellet in a semi-molten state and to impart mechanical strength.
【0012】本発明は前記ごみ焼却灰に、粘結剤、発泡
剤、還元剤および組成制御剤とを添加してペレットを
得、焼成して人工軽量骨材を得るに際し、組成制御剤と
して石炭灰を用いることによって、絶乾比重が1.0〜
1.5g/cm3、一軸圧縮破壊荷重(以下、「圧潰強
度」と示す。)が30kgf以上、かつ吸水率が5%以
下の人工軽量骨材を製造できるというものである。According to the present invention, a binder, a foaming agent, a reducing agent and a composition controlling agent are added to the refuse incineration ash to obtain pellets, which are fired to obtain an artificial lightweight aggregate. By using ash, the absolute dry specific gravity is 1.0 to 1.0
An artificial lightweight aggregate having 1.5 g / cm 3 , a uniaxial compressive breaking load (hereinafter, referred to as “crush strength”) of 30 kgf or more, and a water absorption of 5% or less can be produced.
【0013】本発明の対象となる焼却灰は特に限定され
るものでなく、主灰や飛灰、あるいはその混合物を用い
ることができる。また、前記焼却灰の粒度にも特に影響
されない。組成制御剤として石炭灰を用いるが、石炭灰
中のシリカを焼成時のガラス化に寄与させ、骨材の機械
的強度を増加させる。よって、石炭灰の添加量は骨材用
途に応じて必要とされる物性が得られるよう適宜選択す
ればよいが、絶乾比重1.0〜1.5g/cm3の骨材
を得るには、焼成して得られる骨材のカルシウム含有量
が酸化物換算で16重量%以下となるように石炭灰を添
加することが好ましい。16重量%を越えると最適な焼
成温度域が高くなり、かつ焼成可能な温度幅が狭くな
る。[0013] The incineration ash that is the subject of the present invention is not particularly limited, and main ash, fly ash, or a mixture thereof can be used. Also, it is not particularly affected by the particle size of the incinerated ash. Although coal ash is used as a composition control agent, silica in the coal ash contributes to vitrification at the time of firing, and increases the mechanical strength of the aggregate. Therefore, the amount of coal ash to be added may be appropriately selected so as to obtain required physical properties according to the use of the aggregate, but in order to obtain an aggregate having an absolute dry specific gravity of 1.0 to 1.5 g / cm 3. It is preferable to add coal ash so that the calcium content of the aggregate obtained by firing is 16% by weight or less in terms of oxide. If it exceeds 16% by weight, the optimum firing temperature range becomes high and the temperature range in which firing can be performed becomes narrow.
【0014】石炭灰は火力発電所や石炭焚きボイラ−な
どから発生するものであればよく、特に限定されない
が、例えばフライアッシュとシンダアッシュの混合物で
ある原粉、JISA6201に適合するようなフライア
ッシュ、粗粉、クリンカアッシュを含むすべての石炭灰
を用いることができる。また、石炭灰の粒度も特に限定
されるものではない。また、ある種の石炭灰では未燃カ
−ボンを含むが、このような物を用いると、カーボンが
後述する還元剤としての機能を発揮するため、未燃カ−
ボン量によっては新たに還元剤を添加する必要がないと
いった利点がある。The coal ash is not particularly limited as long as it is generated from a thermal power plant or a coal-fired boiler. For example, the raw powder is a mixture of fly ash and synda ash, and fly ash conforming to JISA6201. All coal ash can be used, including coal, coarse powder and clinker ash. Also, the particle size of the coal ash is not particularly limited. Certain types of coal ash include unburned carbon. However, when such coal is used, the carbon exhibits a function as a reducing agent to be described later.
There is an advantage that it is not necessary to newly add a reducing agent depending on the amount of bon.
【0015】本発明で粘結剤を用いた理由は、加水造粒
後のペレットの成型性と機械的強度を付与するために添
加する。機械的強度が弱いとロータリーキルンでの焼成
の際、ペレットが粉化して製品の収率が低下し、かつ焼
成帯付近でペレット表面に粉化したものが付着したり、
あるいはロータリーキルンの内壁に付着して連続操業に
支障をきたすからである。また粘結剤の種類は特に限定
されないが、例えばベントナイト、水ガラスなどの無機
類、澱粉、糖蜜、リグニン、ポリビニルアルコール、メ
チルセルロース、天然ゴムパルプ廃液などの有機類が挙
げられる。また添加量も特に限定されないが、添加効果
およびコストなどを考慮すると0.5〜10重量%の範
囲が好ましい。The reason for using the binder in the present invention is to add the moldability and mechanical strength of the pellets after the hydration granulation. If the mechanical strength is weak, during firing in a rotary kiln, pellets will be powdered and the product yield will be reduced, and powdered materials will adhere to the pellet surface near the firing zone,
Alternatively, they adhere to the inner wall of the rotary kiln and hinder continuous operation. The type of the binder is not particularly limited, and examples thereof include inorganics such as bentonite and water glass, and organics such as starch, molasses, lignin, polyvinyl alcohol, methylcellulose, and natural rubber pulp waste liquid. The amount of addition is not particularly limited, but is preferably in the range of 0.5 to 10% by weight in consideration of the effect of addition and cost.
【0016】発泡剤と還元剤は、焼成時にペレットの内
部が半溶融状態となったときに、発泡剤と還元剤の作用
によってガスを発生させるために用いる。発生したガス
は気泡としてペレット内部に捕捉され、その量により骨
材の比重が決定される。すなわち、気泡の捕捉量により
比重が調整される。The foaming agent and the reducing agent are used to generate gas by the action of the foaming agent and the reducing agent when the inside of the pellets becomes semi-molten during firing. The generated gas is captured as bubbles in the pellet, and the specific gravity of the aggregate is determined by the amount of the generated gas. That is, the specific gravity is adjusted by the amount of captured bubbles.
【0017】発泡剤や還元剤としては、このような効果
を発揮するものであれば特に限定されないが、本発明で
は発泡剤としては酸化鉄や炭化珪素が、また還元剤とし
ては炭材が好ましく、さらに発泡剤として用いる酸化鉄
としては酸化度の高いヘマタイトが特に好ましい。発泡
剤として用いる酸化鉄の粒度は特に限定されないが、焼
成中の炭材による脱酸素反応を促進するために10μm
以下とすることが好ましい。また、骨材配合原料の全体
に対する好ましいヘマタイトの添加量は、1〜10重量
%である。その理由は1重量%未満では発泡剤としての
効果が少なく、また10重量%を超えて添加しても発泡
による軽量化の効果は増加しないからである。The foaming agent and the reducing agent are not particularly limited as long as they exhibit such effects. In the present invention, the foaming agent is preferably iron oxide or silicon carbide, and the reducing agent is preferably carbonaceous material. Hematite having a high degree of oxidation is particularly preferable as iron oxide used as a foaming agent. The particle size of the iron oxide used as the foaming agent is not particularly limited, but is 10 μm to promote the deoxidation reaction by the carbonaceous material during firing.
It is preferable to set the following. The preferred amount of hematite added is 1 to 10% by weight based on the total amount of the aggregate-mixed raw material. The reason is that if it is less than 1% by weight, the effect as a foaming agent is small, and if it exceeds 10% by weight, the effect of lightening by foaming does not increase.
【0018】炭化珪素は、造粒したペレットが加熱によ
り多量の液相を生成するときに、酸化鉄と効率よく反応
してCO、CO2ガスを発生する。これらのガスを液相
内に捕捉してペレットの発泡膨潤を促進する。骨材配合
原料の全体に対する炭化珪素の添加量は、0.1〜1.
0重量%であることが好ましい。0.1重量%未満では
絶乾比重の軽量化に対する効果が十分でなく、また1.
0重量%を超えても軽量効果は増大しないという理由か
らである。When the granulated pellets generate a large amount of liquid phase by heating, silicon carbide efficiently reacts with iron oxide to generate CO and CO 2 gas. These gases are trapped in the liquid phase to promote foam swelling of the pellets. The amount of silicon carbide to be added to the whole of the aggregate compounding raw material is 0.1-1.
It is preferably 0% by weight. If the content is less than 0.1% by weight, the effect of reducing the absolute dry specific gravity is not sufficient.
This is because even if it exceeds 0% by weight, the light weight effect does not increase.
【0019】還元剤としての炭材は、主として焼成中の
ペレット内部の還元度を調整する役割を果す。効果は小
さいが酸化鉄と反応して発泡作用にも寄与する。炭材と
しては、例えば、石炭やコ−クスなどが挙げられる。な
お、炭化珪素の一部を炭材に置き換えたりすることが可
能である。The carbon material as a reducing agent mainly serves to adjust the degree of reduction inside the pellets during firing. Although the effect is small, it reacts with iron oxide and contributes to the foaming action. Examples of the carbon material include coal and coke. Note that a part of silicon carbide can be replaced with a carbon material.
【0020】骨材配合原料の全体に対する炭材の添加量
は、0.2〜10重量%であることが好ましい。0.2
重量%未満では、発泡による軽量化の効果が得られない
からであり、一方10重量%を超えても発泡膨張による
軽量化効果は増加せず、逆に未燃焼の炭材がペレット内
部に残留して人工軽量骨材の強度を低下させる可能性が
ある。It is preferable that the amount of the carbonaceous material to be added to the whole raw material of the aggregate is 0.2 to 10% by weight. 0.2
If the amount is less than 10% by weight, the effect of reducing the weight by foaming cannot be obtained. On the other hand, if the amount exceeds 10% by weight, the effect of reducing the weight by foaming expansion does not increase, and unburned carbonaceous material remains inside the pellet. As a result, the strength of the artificial lightweight aggregate may be reduced.
【0021】各原材料を混合して得た混合物を粉砕する
方法は、混合した骨材配合原料が平均粒径20μm以
下、好ましくは15μm以下まで微粉砕できるものであ
れば良く、例えばポットミル、振動ミル、遊星ミルなど
のボ−ルミル、衝突式のジェット粉砕機、タ−ボ粉砕機
などが挙げられる。The method of pulverizing the mixture obtained by mixing the respective raw materials is not particularly limited as long as the mixed aggregate-mixed raw material can be finely pulverized to an average particle diameter of 20 μm or less, preferably 15 μm or less. And ball mills such as planetary mills, collision type jet pulverizers and turbo pulverizers.
【0022】つぎに得た粉砕物を、必要に応じて湿式混
練するが、採用する混練方法は特に限定されず公知の混
練装置を用いることができる。また成形方法としては、
所定の径になるように成型できるものであればよく、例
えばパンペレタイザーや押出成型機を用いると簡便であ
る。Next, the obtained pulverized product is wet-kneaded as necessary, but the kneading method to be employed is not particularly limited, and a known kneading apparatus can be used. Also, as a molding method,
What is necessary is just to be able to mold to a predetermined diameter, and for example, it is convenient to use a pan pelletizer or an extruder.
【0023】次いで得られた成型物は必要に応じて乾燥
したあとに焼成するが、焼成法は特に限定されず、例え
ば連続操業や品質の均一性を勘案すればロータリーキル
ンを用いることが好ましく、所望とする骨材物性に合わ
せて雰囲気を任意に選択できる。例えば、燃焼ガス中の
酸素濃度を3〜12%、焼成帯温度を1000〜130
0℃、前記焼成帯温度での成型体の滞留時間を10〜1
20分となるようにキルンの勾配、回転数、ダムの設置
や内径といったキルン構造などを勘案してロ−タリ−キ
ルン操作することが好ましい。なお、焼成前に必要に応
じて施す乾燥法も特に限定されるものでない。Next, the obtained molded product is fired after drying if necessary, but the firing method is not particularly limited. For example, in consideration of continuous operation and uniformity of quality, it is preferable to use a rotary kiln. The atmosphere can be arbitrarily selected according to the physical properties of the aggregate. For example, the oxygen concentration in the combustion gas is 3 to 12%, and the firing zone temperature is 1000 to 130%.
0 ° C., the residence time of the molded body at the firing zone temperature is 10 to 1
It is preferable to perform a rotary kiln operation in consideration of a kiln structure such as a kiln gradient, a rotation speed, a dam installation, and an inner diameter so as to be 20 minutes. In addition, the drying method applied as needed before firing is not particularly limited.
【0024】[0024]
【実施例】以下の実施例および比較例により、本発明を
さらに詳細に説明する。ただし、本発明は下記実施例に
限定されるものではない。なお、用いたごみ焼却飛灰の
主成分は、SiO2:27.36重量%、Al2O3:1
3.00重量%、Fe2O3:1.51重量%、CaO:
15.70重量%、MgO:3.31重量%、Na
2O:8.70重量%、K2O:7.39重量%のもので
ある。また、組成制御剤として用いた石炭灰の主成分
は、SiO2:56.2重量%、Al2O3:32.1重
量%、Fe2O3:3.57重量%、CaO:0.59重
量%、MgO:1.40重量%、Na2O:0.22重
量%、K2O:0.48重量%である。The present invention will be described in more detail with reference to the following Examples and Comparative Examples. However, the present invention is not limited to the following examples. The main components of the used refuse incineration fly ash were SiO 2 : 27.36% by weight and Al 2 O 3 : 1
3.00 wt%, Fe 2 O 3: 1.51 wt%, CaO:
15.70% by weight, MgO: 3.31% by weight, Na
2 O: 8.70% by weight, K 2 O: 7.39% by weight. The main components of the coal ash used as the composition control agent were: SiO 2 : 56.2% by weight, Al 2 O 3 : 32.1% by weight, Fe 2 O 3 : 3.57% by weight, CaO: 0. 59 wt%, MgO: 1.40 wt%, Na 2 O: 0.22 wt%, K 2 O: 0.48 wt%.
【0025】[実施例1]焼却飛灰47.5重量%、ベ
ントナイト5重量%、ヘマタイト5重量%、コークス2
重量%、炭化珪素0.5重量%および石炭灰40重量%
からなる骨材配合原料を、ボールミルを用いて平均粒径
15μmに混合粉砕した。該粉砕物に水を添加しなが
ら、パンペレタイザーで直径約5〜15mmの球状に造
粒した後、105℃で通風乾燥した。次いで、前記乾燥
骨材を煉瓦内径400mm、長さ6000mmのロータ
リーキルンに供給して、燃焼ガス中の酸素濃度5%、温
度約1,120℃の条件下で焼成した。このようにして
得られた骨材aの品質評価として、比重と吸水率はJI
SA1110に基づいて測定し、圧潰強度は圧潰試験機
によって測定した。なお、前記測定は直径約10mmの
各骨材について行い、その平均値を求めた。表1から分
かる通り、実施例1の骨材aは絶乾比重が1.40g/
cm3、圧潰強度が75kgf、吸水率が0.7%であ
った。なお、骨材中の酸化物換算でのカルシウムは化学
分析の結果7.8重量%であった。Example 1 47.5% by weight of incinerated fly ash, 5% by weight of bentonite, 5% by weight of hematite, coke 2
Wt%, silicon carbide 0.5 wt% and coal ash 40 wt%
Was mixed and ground to an average particle size of 15 μm using a ball mill. While adding water to the pulverized product, the mixture was granulated into a spherical shape having a diameter of about 5 to 15 mm using a pan pelletizer, and then dried at 105 ° C. with ventilation. Next, the dried aggregate was supplied to a rotary kiln having a brick inner diameter of 400 mm and a length of 6000 mm, and was fired under the conditions of an oxygen concentration of 5% in combustion gas and a temperature of about 1,120 ° C. As a quality evaluation of the aggregate a thus obtained, specific gravity and water absorption were determined by JI.
The measurement was performed based on SA1110, and the crushing strength was measured using a crushing tester. In addition, the said measurement was performed about each aggregate about 10 mm in diameter, and the average value was calculated | required. As can be seen from Table 1, the aggregate a of Example 1 has an absolute dry specific gravity of 1.40 g /.
cm 3 , crush strength was 75 kgf, and water absorption was 0.7%. In addition, as a result of a chemical analysis, calcium in the aggregate in terms of oxide was 7.8% by weight.
【0026】[実施例2〜4および比較例1〜3]焼却
飛灰57.5重量%、ベントナイト5重量%、ヘマタイ
ト5重量%、コ−クス2重量%、炭化珪素0.5重量%
および石炭灰30重量%とした以外は実施例1と同様に
して骨材b(実施例2)を、焼却飛灰32.5重量%、
ベントナイト5重量%、ヘマタイト5重量%、コ−クス
2重量%、炭化珪素0.5重量%および石炭灰55重量
%とした以外は実施例1と同様にして骨材c(実施例
3)を、焼却飛灰67.5重量%、ベントナイト5重量
%、ヘマタイト5重量%、コ−クス2重量%、炭化珪素
0.5重量%および石炭灰20重量%とし、キルン温度
を1080℃とした以外は実施例1と同様にして骨材d
(実施例4)を、焼却飛灰77.5重量%、ベントナイ
ト5重量%、ヘマタイト5重量%、コ−クス2重量%、
炭化珪素0.5重量%および石炭灰10重量%とした以
外は実施例1と同様にして骨材e(比較例1)を、焼却
飛灰77.5重量%、ベントナイト5重量%、ヘマタイ
ト5重量%、コ−クス2重量%、炭化珪素0.5重量%
および石炭灰10重量%とした以外は実施例4と同様に
して骨材f(比較例2)を、焼却飛灰72.5重量%、
ベントナイト5重量%、ヘマタイト5重量%、コ−クス
2重量%、炭化珪素0.5重量%、石炭灰10重量%お
よび生石灰5重量%とした以外は実施例4と同様にして
骨材g(比較例3)を得た。得られた骨材b〜gについ
て実施例1と同様の測定を行い、その評価結果と骨材中
の酸化物換算でのカルシウムの化学分析結果を表1に併
せて示す。Examples 2 to 4 and Comparative Examples 1 to 3 57.5% by weight of incinerated fly ash, 5% by weight of bentonite, 5% by weight of hematite, 2% by weight of coke, 0.5% by weight of silicon carbide
Aggregate b (Example 2) was prepared in the same manner as in Example 1 except that the amount of coal ash was changed to 30% by weight.
Aggregate c (Example 3) was prepared in the same manner as in Example 1 except that 5% by weight of bentonite, 5% by weight of hematite, 2% by weight of coke, 0.5% by weight of silicon carbide and 55% by weight of coal ash were used. 67.5% by weight of incinerated fly ash, 5% by weight of bentonite, 5% by weight of hematite, 2% by weight of coke, 0.5% by weight of silicon carbide and 20% by weight of coal ash, except that the kiln temperature was 1080 ° C. Is the aggregate d in the same manner as in Example 1.
(Example 4) was obtained by incineration fly ash 77.5% by weight, bentonite 5% by weight, hematite 5% by weight, coke 2% by weight,
Aggregate e (Comparative Example 1) was prepared in the same manner as in Example 1 except that silicon carbide was 0.5% by weight and coal ash was 10% by weight, and incinerated fly ash was 77.5% by weight, bentonite was 5% by weight, and hematite was 5%. Wt%, coke 2 wt%, silicon carbide 0.5 wt%
Aggregate f (Comparative Example 2) was prepared in the same manner as in Example 4 except that coal ash was changed to 10% by weight,
Aggregate g (in the same manner as in Example 4 except that 5% by weight of bentonite, 5% by weight of hematite, 2% by weight of coke, 0.5% by weight of silicon carbide, 10% by weight of coal ash and 5% by weight of quicklime) Comparative Example 3) was obtained. The same measurement as in Example 1 was performed for the obtained aggregates b to g, and the evaluation result and the chemical analysis result of calcium in terms of oxide in the aggregate are shown in Table 1.
【0027】表1から分かる通り、実施例の骨材b〜d
は絶乾比重が1.25〜1.45、圧潰強度が30kg
f以上、吸水率が5%以下であるのに対して、比較例の
骨材eはメルトダウンによって骨材化できず、また比較
例の骨材fは圧潰強度が4kgfと低く、さらに比較例
の骨材gは圧潰強度が30kgf以上であるものの、絶
乾比重が1.5を超えるものであった。As can be seen from Table 1, aggregates b to d of the embodiment are shown.
Has a specific gravity of 1.25 to 1.45 and a crushing strength of 30 kg
f and the water absorption is 5% or less, whereas the aggregate e of the comparative example cannot be made into an aggregate by meltdown, and the aggregate f of the comparative example has a crushing strength as low as 4 kgf. The aggregate g had a crushing strength of 30 kgf or more, but an absolute dry specific gravity of more than 1.5.
【0028】 表1 骨 材 絶乾比重 圧潰強度 吸水率 CaO g/cm2 Kgf % 重量% 実施例1 a 1.40 75 0.7 7.8 実施例2 b 1.45 77 0.5 9.3 実施例3 c 1.25 70 0.1 5.6 実施例4 d 1.30 32 3.0 10.8 比較例1 e 比較例2 f 0.64 4 9.6 12.2 比較例3 g 1.72 57 3.2 22.2Table 1 Aggregate Absolute Dry Specific Gravity Crushing Strength Water Absorption CaO g / cm 2 Kgf% wt% Example 1 a 1.40 75 0.7 7.8 Example 2 b 1.45 77 0.5 9. 3 Example 3 c 1.25 70 0.1 5.6 Example 4 d 1.30 32 3.0 10.8 Comparative Example 1 e Comparative Example 2 f 0.64 4 9.6 12.2 Comparative Example 3 g 1.72 57 3.2 22.2
【0029】[0029]
【発明の効果】以上述べた通り本発明は、ごみ焼却灰を
主原料として高強度でかつ吸水率の低い骨材を効率的に
生産することができる。従って、産業廃棄物を埋め立て
て処理することなく、特に土木・建築材料などに再資源
化できることから、環境保全と資源有効利用において極
めて有用なものである。As described above, the present invention can efficiently produce aggregate having high strength and low water absorption by using refuse incineration ash as a main raw material. Therefore, it is extremely useful in environmental conservation and effective use of resources, since industrial waste can be recycled, especially in civil engineering and building materials, without landfill treatment.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 川本 孝次 千葉県市川市中国分3−18−5住友金属鉱 山株式会社中央研究所内 Fターム(参考) 4D004 AA36 BA02 CA04 CA14 CA30 CC03 CC11 CC13 CC17 CC20 DA03 DA10 ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Koji Kawamoto 3-18-5 China, Ichikawa City, Chiba Prefecture F-term in the Central Research Laboratory of Sumitomo Metal Mining Co., Ltd. 4D004 AA36 BA02 CA04 CA14 CA30 CC03 CC11 CC13 CC17 CC20 DA03 DA10
Claims (3)
剤と、さらに組成制御剤として石炭灰とを混合し、得ら
れた混合物を粉砕し、該粉砕物に水を加えて成型し、該
成型体を要すれば乾燥し、次いで焼成して人工軽量骨材
を得る方法において、最終的に得られる人工軽量骨材中
のカルシウム含有量が、酸化物換算で16重量%以下と
なるように組成制御することを特徴とする人工軽量骨材
の製造方法。1. A waste incineration ash is mixed with a binder, a foaming agent, a reducing agent, and a coal ash as a composition controlling agent, and the resulting mixture is pulverized. In the method of drying the molded body if necessary and then firing it to obtain an artificial lightweight aggregate, the calcium content in the finally obtained artificial lightweight aggregate is 16% by weight or less in terms of oxide. A method for producing an artificial lightweight aggregate, characterized in that the composition is controlled so as to be as follows.
化珪素を用い、前記還元剤として炭材を用いる請求項1
記載の方法。2. The method according to claim 1, wherein iron oxide and / or silicon carbide is used as a foaming agent, and carbonaceous material is used as said reducing agent.
The described method.
られる人工軽量骨材であり、絶乾比重が1.0〜1.5
g/cm3、一軸圧縮破壊荷重が30kgf以上、かつ
吸水率が5%以下であることを特徴とする人工軽量骨
材。3. An artificial lightweight aggregate obtained by the method according to claim 1 or 2, having an absolute dry specific gravity of 1.0 to 1.5.
g / cm 3, a uniaxial compressive breaking load of 30 kgf or more, and a water absorption of 5% or less.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004262728A (en) * | 2003-03-04 | 2004-09-24 | Ube Ind Ltd | Method for producing lightweight aggregate from coal ash and sewage sludge incineration ash |
JP2006122726A (en) * | 2004-10-26 | 2006-05-18 | Kawasaki Heavy Ind Ltd | Granules made from papermaking sludge incineration ash, production method and production apparatus thereof |
CN113788637A (en) * | 2021-10-28 | 2021-12-14 | 中建西部建设建材科学研究院有限公司 | Surface-enhanced internal-curing solid waste-based light aggregate and preparation method thereof |
-
1999
- 1999-03-02 JP JP5341999A patent/JP2000247701A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004262728A (en) * | 2003-03-04 | 2004-09-24 | Ube Ind Ltd | Method for producing lightweight aggregate from coal ash and sewage sludge incineration ash |
JP2006122726A (en) * | 2004-10-26 | 2006-05-18 | Kawasaki Heavy Ind Ltd | Granules made from papermaking sludge incineration ash, production method and production apparatus thereof |
CN113788637A (en) * | 2021-10-28 | 2021-12-14 | 中建西部建设建材科学研究院有限公司 | Surface-enhanced internal-curing solid waste-based light aggregate and preparation method thereof |
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