JP2575963B2 - Manufacturing method of hydraulic material - Google Patents
Manufacturing method of hydraulic materialInfo
- Publication number
- JP2575963B2 JP2575963B2 JP3061679A JP6167991A JP2575963B2 JP 2575963 B2 JP2575963 B2 JP 2575963B2 JP 3061679 A JP3061679 A JP 3061679A JP 6167991 A JP6167991 A JP 6167991A JP 2575963 B2 JP2575963 B2 JP 2575963B2
- Authority
- JP
- Japan
- Prior art keywords
- combustion furnace
- coal ash
- sio
- oxide
- fine particles
- 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 - Fee Related
Links
- 239000000463 material Substances 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000002485 combustion reaction Methods 0.000 claims description 29
- 239000010883 coal ash Substances 0.000 claims description 21
- 239000010419 fine particle Substances 0.000 claims description 21
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 19
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 17
- 239000000292 calcium oxide Substances 0.000 claims description 17
- 239000000112 cooling gas Substances 0.000 claims description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- 239000001301 oxygen Substances 0.000 claims description 10
- 239000000446 fuel Substances 0.000 claims description 9
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 9
- 239000011707 mineral Substances 0.000 claims description 9
- 239000013078 crystal Substances 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 7
- 239000011882 ultra-fine particle Substances 0.000 claims description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000007789 gas Substances 0.000 claims description 6
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 239000002131 composite material Substances 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 239000013618 particulate matter Substances 0.000 claims 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 19
- 238000001816 cooling Methods 0.000 description 15
- 239000007795 chemical reaction product Substances 0.000 description 11
- 239000002893 slag Substances 0.000 description 9
- 239000000428 dust Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 6
- 239000004568 cement Substances 0.000 description 5
- 239000002956 ash Substances 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 4
- 235000019738 Limestone Nutrition 0.000 description 3
- 239000006028 limestone Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000007790 solid phase Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- 239000012159 carrier gas Substances 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003546 flue gas Substances 0.000 description 2
- 239000002440 industrial waste Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000004449 solid propellant Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 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
- C04B7/00—Hydraulic cements
- C04B7/36—Manufacture of hydraulic cements in general
- C04B7/43—Heat treatment, e.g. precalcining, burning, melting; Cooling
- C04B7/44—Burning; Melting
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P40/00—Technologies relating to the processing of minerals
- Y02P40/10—Production of cement, e.g. improving or optimising the production methods; Cement grinding
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、石炭灰より水硬性材料
を製造する方法に関する。The present invention relates to a method for producing a hydraulic material from coal ash.
【0002】[0002]
【従来の技術】代表的な水硬性材料としてはセメントが
あり,その製造方法としては,キルン内で粘土,石灰石
を燃料とともに燃焼,焼成し,焼成物を粉砕微粒化し製
品とする方法が用いられている。2. Description of the Related Art Cement is a typical hydraulic material, and its production method is to burn and burn clay and limestone together with fuel in a kiln, and to pulverize and granulate the burned product into a product. ing.
【0003】[0003]
【発明が解決しようとする課題】セメントは一般に酸化
珪素(SiO2 ),酸化カルシウム(CaO),酸化ア
ルミナ(Al2 O3 )等を主成分として焼成することに
より,C3 S,β−C2S,C2 A(C:CaO,S:
SiO2 ,A:Al2 O3 )等を成分とする平均粒径1
5〜20μ程度の微粒子で,これに水を添加混合するこ
とにより,これらの成分が水酸基と反応し,ポゾラン生
成物を生じて硬化体を生成するものである。これらの成
分比率により各種セメントが製造されているが,製品粒
度又は結晶形に関しては余り関心が払われていない。し
かし,近年コンクリートの高性能化の観点から,製品の
微粒化と,非晶質形指向が検討されている。Generally, cement is fired mainly with silicon oxide (SiO 2 ), calcium oxide (CaO), alumina oxide (Al 2 O 3 ) or the like to obtain C 3 S, β-C 2 S, C 2 A (C: CaO, S:
SiO 2 , A: Al 2 O 3 )
Fine particles of about 5 to 20 μm are added to and mixed with water, and these components react with hydroxyl groups to produce a pozzolan product to form a cured product. Various cements have been produced with these component ratios, but little attention has been paid to the product particle size or crystal form. However, in recent years, from the viewpoint of improving the performance of concrete, refinement of products and orientation of amorphous forms have been studied.
【0004】一方,石炭灰はセメントの構成成分である
SiO2 ,Al2 O3 を多量に含み,またCaOも少量
であるが若干含んでいて,水硬性材料として利用できる
成分を含有している。[0004] On the other hand, coal ash contains a large amount of SiO 2 and Al 2 O 3 which are constituents of cement, and also contains a small amount of CaO in a small amount, and contains a component usable as a hydraulic material. .
【0005】本発明は,以上の点に着目してなされたも
のであって,石炭焚きボイラ等から多量に発生し産業廃
棄として投棄されている石炭灰を有効に利用して水硬性
の良い水硬性材料を製造する方法を提供しようとするも
のである。The present invention has been made in view of the above points, and effectively utilizes coal ash generated in large quantities from coal-fired boilers and the like and discarded as industrial waste, and has good hydraulicity. It is intended to provide a method for producing a hard material.
【0006】[0006]
【課題を解決するための手段】前記の課題を解決する手
段として,本発明の水硬性材料の製造方法は,次の手段
を採用した。As a means for solving the above-mentioned problems, the method for producing a hydraulic material of the present invention employs the following means.
【0007】(1) 酸化珪素(SiO2 ),酸化アルミ
ナ(Al2 O3 )を等の鉱物物質で構成される石炭灰を
燃料を酸素又は酸素富化空気で燃焼させる2400℃以
上の高温場を形成する燃焼炉内へ供給し,石炭灰中の低
沸点物質であるSiO2 を選択的に気化させる。(1) Coal ash composed of mineral substances such as silicon oxide (SiO 2 ) and alumina oxide (Al 2 O 3 ) is burned with oxygen or oxygen-enriched air as a fuel. fed into the combustion furnace to form a selectively vaporize the SiO 2 which is a low boiling substance in the coal ash.
【0008】(2) 燃焼炉出口部で冷却ガスにより,燃
焼ガス中に含まれる気化されたSiO 2 蒸気を冷却凝結
し,SiO2 成分に富む固体超微粒子を生成させる。(2) Combustion at the outlet of the combustion furnace
Evaporated SiO contained in the firing gas TwoCooling and condensing steam
And SiOTwoIt produces solid ultrafine particles rich in components.
【0009】(3) 酸化カルシウム(CaO)又は炭酸
カルシウム(CaCO3 )の微粒子(たとえば石灰石の
微粒子)を燃焼炉出口部へ供給し燃焼炉から排出される
高温の排ガス中に混合し,成分的にSiO2 ,Al2 O
3 ,SiO又はこれらの複合結晶物の微粒子物質を生成
させる。(3) Fine particles of calcium oxide (CaO) or calcium carbonate (CaCO 3 ) (for example, fine particles of limestone) are supplied to the outlet of the combustion furnace, mixed with high-temperature exhaust gas discharged from the combustion furnace, and subjected to mixing. SiO 2 and Al 2 O
3 , to produce fine particles of SiO or composite crystals thereof.
【0010】(4) 同微粒子物質を冷却した上捕集して
水硬性微粒子を得る。(4) The fine particles are cooled and collected to obtain hydraulic fine particles.
【0011】[0011]
【作用】前項に於いて述べた各階段に於ける作用は下記
の通りである。[Operation] The operation in each step described in the previous section is as follows.
【0012】(1) の段階では,石炭灰中のSiO2 の
1部気化と気化した後の石炭灰の飛び出し飛散過程を持
たせるもので,SiO2 の気化量と石炭灰からの飛散微
粒子量の割合及び量がコントロールされる。これは燃焼
炉形状,バーナ配置,燃焼量等により調整される。In the step (1), a part of the SiO 2 in the coal ash is vaporized, and the coal ash is leached and scattered after the vaporization. The amount of the vaporized SiO 2 and the amount of the scattered fine particles from the coal ash are provided. Is controlled. This is adjusted by the shape of the combustion furnace, the burner arrangement, the amount of combustion, and the like.
【0013】(2) 〜 (3) の段階では,燃焼炉から排
出されたSiO2 蒸気を冷却ガスにより冷却しSiO2
成分に富む0.1μ以下の超微粒子を生成し,併わせて
CaO又はCaCO3 の微粒子を燃焼炉出口部の高温の
排ガス中に混合して,このCaO又はCaCO3 の微粒
子と前記のSiO2 成分に富む超微粒子と石炭灰からの
飛散微粒子を反応させて,成分的にSiO2 ,Al2 O
3 ,SiO2 又はこれらの複合結晶物の微粒子物質を生
成する。[0013] (2) At the stage of ~ (3), cooling the SiO 2 steam discharged from the combustion furnace by the cooling gas SiO 2
Generates a 0.1μ following ultrafine particles-rich component, a mixture of CaO or CaCO 3 particulate into the hot flue gas of the combustion furnace outlet Te併Align, SiO 2 of the fine particles of the CaO or CaCO 3 reacting the scattering particles from fine particles and coal ash rich component, component to SiO 2, Al 2 O
3 , to produce fine particles of SiO 2 or composite crystals thereof.
【0014】(4) の段階では,前記の微粒子物質を冷
却して,その結晶形の変更を図ると共に,同超微粒子物
質の冷却を行い,捕集する。本段階では冷却ガスの投入
量を調節する等の手段により,反応生成物である超微粒
子物質の冷却速度を変えることにより反応生成物の結晶
形を変化させる。例えば,冷却速度が小さい場合には,
反応生成物は結晶型生成物となる。逆に冷却速度が大き
い場合には非晶質型生成物となる。なお,冷却速度が小
さい場合とは,100℃/min 〜500℃/min で,冷
却速度が大きい場合とは,100℃/sec 〜500℃/
sec 程度である。In the step (4), the above-mentioned fine particle material is cooled to change its crystal form, and the ultra-fine particle material is cooled and collected. In this stage, the crystal form of the reaction product is changed by changing the cooling rate of the ultrafine particle material as the reaction product by means such as adjusting the amount of cooling gas input. For example, if the cooling rate is low,
The reaction product becomes a crystalline product. Conversely, when the cooling rate is high, an amorphous type product is obtained. The case where the cooling rate is low is 100 ° C / min to 500 ° C / min, and the case where the cooling rate is high is 100 ° C / sec to 500 ° C / min.
sec.
【0015】[0015]
【実施例】本発明の一実施例に係る水硬性材料の製造方
法の系統を図1に示す。FIG. 1 shows a system of a method for producing a hydraulic material according to one embodiment of the present invention.
【0016】図1において,1は冷却壁で構成され燃料
を酸素又は酸素富化空気で燃焼して2400℃以上の高
温燃焼場を形成する燃焼炉,2は燃焼炉の後流煙道,3
は石炭灰供給装置,4はCaO含有鉱物質供給装置,5
は粗集じん器,6は精密集じん器,7は燃焼炉2より流
下する溶融スラグ,8はスラグタンク,9は粗集じん器
5と精密集じん器6で捕集された水硬性材料,10は燃
焼炉壁を流下する溶融スラグを示す。In FIG. 1, reference numeral 1 denotes a combustion furnace which is constituted by a cooling wall and burns fuel with oxygen or oxygen-enriched air to form a high-temperature combustion field of 2400 ° C. or higher, 2 denotes a flue gas downstream of the combustion furnace, 3
Is a coal ash feeder, 4 is a CaO-containing mineral feeder, 5
Is a coarse dust collector, 6 is a precision dust collector, 7 is molten slag flowing down from the combustion furnace 2, 8 is a slag tank, 9 is a hydraulic material collected by the coarse dust collector 5 and the precision dust collector 6. , 10 indicate molten slag flowing down the combustion furnace wall.
【0017】図1中の細実線は燃焼を冷却水系,太実線
は燃料系,細一点鎖線は石炭灰供給系,細二点鎖線は酸
素又は富化酸素供給系,太一点鎖線はCaO含有鉱物質
供給系,太破線は冷却ガス供給系の各系統を示す。In FIG. 1, a thin solid line represents a cooling water system for combustion, a thick solid line represents a fuel system, a thin dashed line represents a coal ash supply system, a thin two-dot chain line represents an oxygen or enriched oxygen supply system, and a thick dashed line represents a CaO-containing mineral. The quality supply system and the bold broken lines indicate the respective systems of the cooling gas supply system.
【0018】燃焼炉1に供給される燃料は,石炭等の固
体燃料,又はガス状燃料,液体燃料が用いられ,また燃
料系統と酸素又は酸素富化空気供給系統は複数系統で構
成される。冷却ガスは空気の他,水蒸気,窒素等の不活
性ガスでも良く,かつ,冷却ガスは,燃焼炉後の流煙道
2の数ケ所から段階的に導入されるようになっている。The fuel supplied to the combustion furnace 1 is a solid fuel such as coal, a gaseous fuel, or a liquid fuel. The fuel system and the oxygen or oxygen-enriched air supply system are composed of a plurality of systems. The cooling gas may be an inert gas such as water vapor or nitrogen, in addition to air, and the cooling gas is introduced stepwise from several places in the flue 2 after the combustion furnace.
【0019】図1において,石炭灰は石炭灰供給装置3
から搬送空気により搬送され,燃焼炉1内の2400℃
以上の高温燃焼場へ供給される。供給石炭灰は高温燃焼
場で溶融し,溶融石炭灰中のSiO2 は1部気化し,残
部は冷却炉壁へ捕捉され溶融スラグ10として流下燃焼
炉系外へ溶融スラグ7として,排出スラグタンク8へ排
出される。In FIG. 1, coal ash is supplied to a coal ash supply device 3.
2400 ° C in the combustion furnace 1
It is supplied to the above high-temperature combustion field. The supplied coal ash is melted in the high-temperature combustion field, one part of the SiO 2 in the molten coal ash is vaporized, and the remainder is captured by the cooling furnace wall as molten slag 10 as molten slag out of the downstream combustion furnace system as a discharged slag tank. It is discharged to 8.
【0020】一方,気化SiO2 蒸気と石炭灰空飛出し
た微粒子溶融灰を含む燃焼ガスは,燃焼炉1の上部から
燃焼炉の後流煙道2へ排気され,同煙道2へ導入される
冷却ガスにより,約200℃/sec の冷却速度で順次冷
却され,冷却される段階で,SiO2 蒸気は凝結して
0.1μ以下の固体超微粒子に,また微粒子溶融灰は冷
却固化して数μ以下の微粒子となる。この過程でSiO
2 蒸気は気相−液相−固相へ相変化し,微粒子溶融灰は
液相−固相へと相変化する。On the other hand, the combustion gas containing the vaporized SiO 2 vapor and the fine particle molten ash that has flew out of the coal ash is exhausted from the upper part of the combustion furnace 1 to the flue 2 downstream of the combustion furnace, and introduced into the flue 2. The cooling gas is sequentially cooled at a cooling rate of about 200 ° C./sec. At the cooling stage, the SiO 2 vapor condenses to solid ultrafine particles of 0.1 μ or less, and the fine particle molten ash cools and solidifies. It becomes fine particles of several μ or less. In this process, SiO
(2) The vapor changes its phase from a gas phase to a liquid phase to a solid phase, and the particulate ash changes its phase to a liquid phase to a solid phase.
【0021】この冷却ガス導入過程で,数μに微粒化さ
れたCaO含有鉱物質が供給装置4より燃焼炉1の出口
部の後流煙道2へ搬送ガスにより供給される。この搬送
ガスは冷却ガスと供用するようにしてもよい。In this cooling gas introduction process, the CaO-containing mineral matter atomized to several μm is supplied from the supply device 4 to the downstream flue 2 of the outlet of the combustion furnace 1 by a carrier gas. This carrier gas may be used together with the cooling gas.
【0022】供給されたCaO含有鉱物質(たとえば石
灰石)は高温排ガス中に混合され,同排ガス中に存在す
る気相,液相,又は固相状態にあるSiO2 ,及び液
相,固相状態にある微粒子溶融灰と混合しSiO2 ,A
l2 O3 等とCaOとの微粒子反応物を生成する。この
微粒子反応物は,供給されるCaO含有鉱物質の大きさ
数μと平均的に同じ大きさを有する。The supplied CaO-containing mineral substance (eg, limestone) is mixed into the high-temperature exhaust gas, and SiO 2 in the gaseous phase, liquid phase, or solid phase present in the high-temperature exhaust gas, and the liquid phase, solid state mixed with fine molten ash in the SiO 2, a
A particulate reaction product of l 2 O 3 and the like with CaO is generated. This particulate reactant has on average the same size as the several μm of CaO-containing mineral supplied.
【0023】反応生成物は更に冷却ガスにより冷却さ
れ,この冷却速度を適当に設定することにより,反応生
成物の結晶形の相違する水硬性材料が生成される。The reaction product is further cooled by a cooling gas, and by setting this cooling rate appropriately, a hydraulic material having a different crystal form of the reaction product is produced.
【0024】一般に冷却速度を速くすると非晶質に,徐
冷すると結晶形とすることができる。また,水硬性材料
の各成分比は,CaO含有鉱物質の供給量を変化させる
ことにより,任意に調整できる。In general, it can be made amorphous by increasing the cooling rate, and can be made crystalline by slow cooling. The ratio of each component of the hydraulic material can be arbitrarily adjusted by changing the supply amount of the CaO-containing mineral substance.
【0025】以上のように冷却された超微粒子の反応生
成物は,粗集じん器5及び精密集じん器6で捕集され,
超微粒子の水硬性材料9が得られる。The reaction product of the ultra-fine particles cooled as described above is collected by the coarse dust collector 5 and the fine dust collector 6,
An ultrafine hydraulic material 9 is obtained.
【0026】[0026]
【発明の効果】本発明による水硬性材料の製造方法で
は,下記の効果をもつ。The method for producing a hydraulic material according to the present invention has the following effects.
【0027】(1) 産業廃棄物として廃棄処分されてい
る石炭灰を有効に利用することができる。(1) Coal ash discarded as industrial waste can be effectively used.
【0028】(2) 石炭灰は高温場での処理とその後の
冷却により,0.1μ以下の超微粒SiO2 粒子と数μ
以下の微粒子となる。(2) Coal ash is treated in a high temperature field and then cooled to form ultrafine SiO 2 particles of 0.1 μm or less and several μm.
The following fine particles are obtained.
【0029】また,CaO又はCaCO3 の微粒子が供
給されるため,結果的に合成される反応生成物(即ち,
水硬性材料)は,平均的にCaO又はCaCO3 の微粒
子と同大きさの微粒子反応生成物となる。CaO又はC
aCO3 を粉砕して数μとすることは容易であって,こ
の場合には平均的に数μの微粒子反応生成物が生成さ
れ,これは従来のセメントと比較して1オーダ小さいた
め,コンクリートとして使用する場合反応性を活性化す
る効果をもつ。Further, since the fine particles of CaO or CaCO 3 are supplied, the reaction product synthesized as a result (ie,
The hydraulic material) is a fine particle reaction product having the same size as the fine particles of CaO or CaCO 3 on average. CaO or C
It is easy to pulverize aCO 3 to several μm. In this case, a few μm fine particle reaction product is generated on average, which is one order of magnitude smaller than that of conventional cement. When used as an active ingredient, it has the effect of activating the reactivity.
【0030】(3) 反応生成物は冷却ガスによる冷却速
度の調整により結晶形を変化できる。特に冷却速度を速
くすることによって,非晶質形とすることができるた
め,これもコンクリートとして使用する場合反応性を活
性化することができる。(3) The crystal form of the reaction product can be changed by adjusting the cooling rate with a cooling gas. In particular, by increasing the cooling rate, an amorphous form can be obtained, so that when it is also used as concrete, the reactivity can be activated.
【図1】本発明の一実施例の系統図である。FIG. 1 is a system diagram of one embodiment of the present invention.
1 燃焼炉 2 後流煙道 3 石炭灰供給装置 4 CaO含有鉱物質供給装置 5 粗集じん器 6 精密集じん器 7 溶融スラグ 8 スラグタンク 9 水硬性材料 10 溶融スラグ REFERENCE SIGNS LIST 1 combustion furnace 2 wake flue 3 coal ash supply device 4 CaO-containing mineral substance supply device 5 coarse dust collector 6 precision dust collector 7 molten slag 8 slag tank 9 hydraulic material 10 molten slag
Claims (1)
成される石炭灰を燃料を酸素又は酸素富空気で燃焼させ
2,400℃以上の高温燃焼場を形成する燃焼炉内へ供
給し,当該石炭灰中の低沸点物質である酸化珪素を選択
的に気化させ,その気化蒸気を燃焼炉出口において冷却
ガスにより冷却,凝結させ,酸化珪素成分に富む固体超
微粒子を生成させるとともに,燃焼炉出口部へ酸化カル
シウム又は炭酸カルシウムの微粒子を供給し同出口部の
高温の排ガス中に混合して成分的に酸化珪素,酸化アル
ミナ,酸化カルシウム又は,これらの複合結晶物の微粒
子物質を生成させ,同微粒子物質を冷却した上捕集する
ことを特徴とする水硬性材料の製造方法。1. A coal ash composed of a mineral substance such as silicon oxide or alumina oxide is supplied to a combustion furnace which forms a high-temperature combustion field of 2,400 ° C. or higher by burning fuel with oxygen or oxygen-rich air, Silicon oxide, which is a low-boiling substance in the coal ash, is selectively vaporized, and the vaporized vapor is cooled and condensed with a cooling gas at a combustion furnace outlet to produce solid ultrafine particles rich in silicon oxide components, and the combustion furnace Fine particles of calcium oxide or calcium carbonate are supplied to the outlet portion and mixed with high-temperature exhaust gas at the outlet portion to form silicon oxide, alumina oxide, calcium oxide, or fine particles of these composite crystals as components, A method for producing a hydraulic material, wherein the particulate matter is cooled and collected.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3061679A JP2575963B2 (en) | 1991-03-26 | 1991-03-26 | Manufacturing method of hydraulic material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3061679A JP2575963B2 (en) | 1991-03-26 | 1991-03-26 | Manufacturing method of hydraulic material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06183796A JPH06183796A (en) | 1994-07-05 |
| JP2575963B2 true JP2575963B2 (en) | 1997-01-29 |
Family
ID=13178191
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3061679A Expired - Fee Related JP2575963B2 (en) | 1991-03-26 | 1991-03-26 | Manufacturing method of hydraulic material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2575963B2 (en) |
-
1991
- 1991-03-26 JP JP3061679A patent/JP2575963B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06183796A (en) | 1994-07-05 |
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