JPH0749100B2 - Method for producing inorganic spherical particles - Google Patents
Method for producing inorganic spherical particlesInfo
- Publication number
- JPH0749100B2 JPH0749100B2 JP63259042A JP25904288A JPH0749100B2 JP H0749100 B2 JPH0749100 B2 JP H0749100B2 JP 63259042 A JP63259042 A JP 63259042A JP 25904288 A JP25904288 A JP 25904288A JP H0749100 B2 JPH0749100 B2 JP H0749100B2
- Authority
- JP
- Japan
- Prior art keywords
- temperature
- cooling
- chamber
- gas
- amount
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B13/00—Oxygen; Ozone; Oxides or hydroxides in general
- C01B13/14—Methods for preparing oxides or hydroxides in general
- C01B13/34—Methods for preparing oxides or hydroxides in general by oxidation or hydrolysis of sprayed or atomised solutions
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/113—Silicon oxides; Hydrates thereof
- C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
- C01B33/18—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof
- C01B33/181—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof by a dry process
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/30—Particle morphology extending in three dimensions
- C01P2004/32—Spheres
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Silicon Compounds (AREA)
- Glanulating (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、無機質粉末原料から球状化粒子を製造する方
法と装置に関し、品質の安定した状態で球状粒子を経済
的に増減産できる方法に関する。TECHNICAL FIELD The present invention relates to a method and an apparatus for producing spheroidized particles from an inorganic powder raw material, and to a method for economically increasing or decreasing the production of spherical particles in a stable quality state. .
従来、例えば封止剤として用いられる溶融シリカ等の無
機質粒子の製造技術として、例えば特開昭62−241541号
公報、及び特開昭62−241542号公報により無機質粉末を
燃料ガス/酸素バーナーへ供給し、その燃焼域で溶融粒
子とした後、連接する冷却域で冷却気体(例えば空気)
を吹き込み急速冷却し、粒子の融着を防止する技術が提
案されている。Conventionally, as a technique for producing inorganic particles such as fused silica used as a sealing agent, for example, JP-A-62-241541 and JP-A-62-241542 provide inorganic powder to a fuel gas / oxygen burner. Then, after forming molten particles in the combustion area, cooling gas (for example, air) in the cooling area connected to it
A technique has been proposed in which the particles are blown and rapidly cooled to prevent fusion of particles.
従来技術において、基準操業に対し増産又は減産の要請
があった場合、品質を高位に保ちつつこれに対処するこ
とは、バーナー負荷の変更可能な狭い範囲内でしかでき
なかった。即ち、これらに使用される燃料ガス/酸素バ
ーナーは、その燃焼速度が大きく、バーナーノズル部流
速が燃焼速度を下回ると逆火現象を生じ、一瞬にしてバ
ーナー溶損トラブルを発生する。このため、燃焼負荷の
変更可能範囲は、約75〜100%と見られている。In the prior art, when there was a demand to increase or decrease the production for the standard operation, it was possible to cope with this while keeping the quality at a high level, only within a narrow range where the burner load could be changed. That is, the fuel gas / oxygen burner used for these has a high burning rate, and when the flow velocity of the burner nozzle portion is lower than the burning rate, a flashback phenomenon occurs, and burner melting damage trouble occurs in an instant. Therefore, the changeable range of the combustion load is considered to be about 75 to 100%.
バーナーへ供給される無機質粉末原料は、容易に増減量
(増減産)できるが、燃焼負荷に対して過度に供給され
ると火炎温度の低下により球状化率が低下し、品質の良
い球状粒子が得られない。The amount of the inorganic powder raw material supplied to the burner can be easily increased / decreased (increased / decreased production), but if it is excessively supplied to the combustion load, the spheroidization rate will decrease due to the decrease in flame temperature, and good quality spherical particles will be produced. I can't get it.
一方、減産の場合、燃焼負荷の低下に比例して粉末原料
の供給量を減量していくが、バーナーの下限値により限
界となる。下限燃料負荷の状態でさらに粉末原料の供給
量を減少させていくと粉末が高温火炎中に長時間滞留す
ることとなり、溶融物同士の融着により粗大化し粗粒比
率が増大する。On the other hand, in the case of production reduction, the supply amount of the powder raw material is reduced in proportion to the reduction of the combustion load, but this is limited by the lower limit value of the burner. If the supply amount of the powder raw material is further reduced under the condition of the lower limit fuel load, the powder will stay in the high temperature flame for a long time, and the fusion of the melts will cause coarsening and increase of the coarse particle ratio.
本発明者等の検討によれば、この冷却室内に供給された
冷却気体は球状固化後冷却室下方より後続の系内へ排出
されるが、一部の冷却気体は上方の球状化室へ上昇して
いく。According to the study by the present inventors, the cooling gas supplied into the cooling chamber is discharged into the subsequent system from the lower side of the cooling chamber after spherical solidification, but a part of the cooling gas rises to the upper spherical chamber. I will do it.
そしてこの上昇した冷却気体は、燃料ガス/酸素バーナ
ーにより形成される燃焼火炎に巻き込まれてその火炎温
度を低下させ、無機質粉末原料の溶融効果を下げている
ことが判明した。It has been found that the increased cooling gas is caught in the combustion flame formed by the fuel gas / oxygen burner to lower the flame temperature and lower the melting effect of the inorganic powder raw material.
本発明は、上記の現象から冷却気体の供給量をコントロ
ールするならば、球状化室の火炎温度を自在にコントロ
ールできることに着目し、この冷却気体供給量のコント
ロールによる火炎温度の制御による球状化粒子の増減産
を容易に可能としたものである。The present invention focuses on the fact that the flame temperature in the spheroidizing chamber can be freely controlled if the cooling gas supply amount is controlled from the above phenomenon, and the spheroidized particles by controlling the flame temperature by controlling the cooling gas supply amount. It is possible to easily increase or decrease the production.
本発明は、 (1)球状化室と冷却室を有する竪形炉の球状化室で高
温火炎と無機質粉末原料とを接触させて球状化処理した
後、冷却室内で冷却気体を供給して冷却する無機質球状
粒子の製造方法において、無機質粉末原料の供給量に応
じて冷却用気体の供給量を調整し、高温火炎温度を制御
することを特徴とする無機質球状粒子の製造方法であ
る。The present invention includes (1) a high temperature flame and an inorganic powder raw material are brought into contact with each other in a spheroidizing chamber of a vertical furnace having a spheroidizing chamber and a cooling chamber for spheroidizing treatment, and then a cooling gas is supplied to cool the pulverizing chamber. In the method for producing inorganic spherical particles, the amount of cooling gas supplied is adjusted according to the amount of the inorganic powder raw material supplied to control the high temperature flame temperature.
以下にシリカの球状粒子製造設備を例にとり、本発明を
説明する。The present invention will be described below by taking a facility for producing spherical particles of silica as an example.
球状化率を簡易的に表現する指数として、ガラス化率が
採用されているが、これはガラスの真比重(2.21)と、
石英の真比重(2.65)に着目し製品の真比重(A)より
次式で推算している。The vitrification rate is used as an index that simply expresses the spheroidization rate. This is the true specific gravity of glass (2.21),
Focusing on the true specific gravity of quartz (2.65), it is estimated from the true specific gravity of the product (A) using the following formula.
ガラス比率(%)=(13.3/A−5.02)×100 第1図に、火炎温度と噴射された粒子の温度上昇に関す
る計算結果を示すが、火炎温度はバーナー口より通ざか
るに従いシリカへの伝熱,熱損失や周辺ガスの巻き込み
によって、低下していく。Glass ratio (%) = (13.3 / A-5.02) x 100 Figure 1 shows the calculation results for the flame temperature and the temperature rise of the injected particles. The flame temperature is transmitted to silica as it passes through the burner port. It decreases due to heat, heat loss, and entrainment of surrounding gas.
今、第1図に示すような温度分布の火炎(a)の場合、
溶融化のためには粉体噴射量が200kg/Hの場合適当であ
るが、120kg/Hでは高すぎる、即ち、融点以上に加熱さ
れ粒子同士の合体によって粗粒化を起こす。一方280kg/
Hでは温度が低すぎ融点に達しないことからガラス化率
の低い製品となる。噴射量120kg/Hの場合の理想的な火
炎温度分布としては第1図点線で示す火炎温度bであ
り、溶融が完了する距離で火炎温度が融点まで低下して
きていることが望ましい。Now, in the case of a flame (a) having a temperature distribution as shown in FIG.
For melting, a powder injection amount of 200 kg / H is suitable, but 120 kg / H is too high, that is, the particles are heated to a temperature higher than the melting point to cause coarsening due to coalescence of particles. Meanwhile 280 kg /
With H, the temperature is too low to reach the melting point, so the product has a low vitrification rate. The ideal flame temperature distribution when the injection amount is 120 kg / H is the flame temperature b shown by the dotted line in FIG. 1, and it is desirable that the flame temperature be lowered to the melting point at the distance where melting is completed.
溶射バーナーの火炎は、周辺ガスを巻き込みながら拡散
していくが、バーナーより1m地点でおよそ燃焼ガス量の
1〜5倍の周辺ガスを巻き込んでいる事が、調査の結果
判明した。バーナーより1m地点で周辺ガスを燃焼ガス量
の1.5倍巻き込んでいる場合、火炎の熱損失を無視して1
m地点の火炎温度を推定すると、周辺温度が800℃のとき
は火炎温度は1480℃、周辺温度が1200℃のときは火炎温
度は1720℃となり、周辺ガス温度を変化させることによ
って火炎温度を調節できることが判る。周辺ガス温度を
変化させる手段として、冷却室に吹きこむ冷却気体(こ
こでは清浄空気を使用)の量を増減することを検討した
ところ第2図に示す如き結果を得た。As a result of the investigation, it was found that the flame of the thermal spray burner diffuses while entraining the surrounding gas, but entrains 1 to 5 times the amount of the combustion gas around the burner at 1 m from the burner. When surrounding gas is entrained 1.5 times as much as combustion gas at 1m from burner, ignore heat loss of flame and
Estimating the flame temperature at the m point, the flame temperature is 1480 ° C when the ambient temperature is 800 ° C, 1720 ° C when the ambient temperature is 1200 ° C, and the flame temperature is adjusted by changing the ambient gas temperature. I know what I can do. As a means for changing the ambient gas temperature, it was examined to increase or decrease the amount of cooling gas (clean air is used here) blown into the cooling chamber, and the results shown in FIG. 2 were obtained.
この結果を活用すれば、無機質粉末の噴射量の少ない時
には粒子が高温となり合体してえ粗粒化するので、これ
を防ぐために冷却空気流量の増大により火炎温度を下
げ、粉体の噴射量を増大する時には、冷却空気流量を減
少させ火炎温度を上げる事によって品質の安定を図るこ
とができる。If this result is utilized, when the injection amount of the inorganic powder is small, the particles become high temperature and coalesce into coarse particles, so to prevent this, the flame temperature is lowered by increasing the cooling air flow rate, and the injection amount of the powder is reduced. When increasing, it is possible to stabilize the quality by decreasing the cooling air flow rate and raising the flame temperature.
しかしながら、冷却室出口排出ガス量や温度が変動する
と後工程の球状粒子分離設備やガス処理設備の操業が不
安定となる。そこで本発明装置では、別途冷却気体の増
減分に見合った量の気体を冷却室出口配管部へ補給する
ことによってプロセス全体の熱,ガス量バランスをとる
ものである。However, if the amount of exhaust gas or temperature at the outlet of the cooling chamber fluctuates, the operation of the spherical particle separation equipment or gas treatment equipment in the subsequent process becomes unstable. Therefore, in the apparatus of the present invention, the heat and gas amounts of the entire process are balanced by separately replenishing the cooling chamber outlet pipe with an amount of gas corresponding to the increase or decrease of the cooling gas.
第3図に示す本発明の実施態様を示す装置例において、
球状化室1の天井部に設けられた溶射バーナー3より無
機質粉末原料,燃料ガス,酸素が球状化室1へ噴射され
る。球状化室下方に連接せる冷却室2には、冷却気体が
同調節弁6を経て吹き込まれ、球状化室1よりの高温火
炎と溶融粒子を冷却している。球状粒子と燃焼排ガス
は、冷却室2下部より気送管10を通して粒子,ガスの処
理工程へ送られる。この冷却室2の下部には粗粒子の排
出弁8,9が設けられ無機質溶融物や、脱落した耐火物等
を定期的に排出している。In the apparatus example showing the embodiment of the present invention shown in FIG.
An inorganic powder raw material, fuel gas, and oxygen are injected into the spheroidizing chamber 1 from a thermal spray burner 3 provided on the ceiling of the spheroidizing chamber 1. Cooling gas is blown into the cooling chamber 2 connected to the lower side of the spheroidizing chamber through the regulating valve 6 to cool the high temperature flame and the molten particles from the spheroidizing chamber 1. The spherical particles and the combustion exhaust gas are sent from the lower part of the cooling chamber 2 to the particle and gas treatment process through the air feeding pipe 10. Discharge valves 8 and 9 for coarse particles are provided in the lower portion of the cooling chamber 2 to regularly discharge the inorganic molten material, the refractory material and the like that have fallen off.
ここでは、冷却気体として空気が用いられ、ファン4よ
りの空気はフィルターにてダスト除去された後、冷却気
体として調節弁6を経て冷却室2へ吹き込まれる。本発
明装置では、この冷却空気を分岐し、冷却室出口気送管
10と球状粒子が1次分離されるサイクロン11の上流側に
調節弁7を介して供給できるように配管した。冷却空気
流量は、球状化室1を上昇するガス温度を検知する温度
計13によって調節され、無機質粉末原料の噴射量が多い
時には、冷却空気の減量により球状化室温度が高温とさ
れ、逆に粉末原料の噴射量が少ない時には、冷却空気が
増量され球状化室温度が下げられる。Here, air is used as the cooling gas, and the air from the fan 4 is dust-removed by the filter and then blown into the cooling chamber 2 as the cooling gas through the control valve 6. In the device of the present invention, this cooling air is branched and the cooling chamber outlet air feeding pipe is branched.
A piping was provided so that 10 and spherical particles could be supplied through a control valve 7 to the upstream side of a cyclone 11 where primary separation was performed. The flow rate of the cooling air is adjusted by a thermometer 13 that detects the temperature of the gas rising in the spheroidizing chamber 1. When the injection amount of the inorganic powder raw material is large, the spheroidizing chamber temperature is increased due to the reduction of the cooling air, and conversely. When the injection amount of the powder raw material is small, the cooling air is increased and the spheroidizing chamber temperature is lowered.
このようにして粉末原料の融着による粗粒化を防止しな
がら、高ガラス化率の球状製品を安定して得ることがで
きるが、冷却室から排出されるガス量と温度が変動する
ことによって、サイクロンの如き遠心分離装置では、そ
の分離粒子径分布が異なって来ることから本実施例で
は、サイクロン11の入口側へ冷却空気を補給できるよう
にし、調節弁7により冷却空気流量を調節して、サイク
ロン11より分離されてくる粒子径を制御すると共に下工
程における粒子分離やガス処理を容易にした。次に、上
記装置による操業の実施例を示す。In this way, it is possible to stably obtain a spherical product with a high vitrification rate while preventing coarsening due to fusion of the powder raw material, but the amount of gas discharged from the cooling chamber and the temperature change In a centrifugal separator such as a cyclone, the separated particle size distribution is different. Therefore, in this embodiment, cooling air can be supplied to the inlet side of the cyclone 11, and the cooling air flow rate is adjusted by the control valve 7. The particle size of particles separated from the cyclone 11 was controlled, and particle separation and gas treatment in the lower step were facilitated. Next, an example of operation by the above apparatus will be described.
基準操業として、溶射バーナー3へ燃料ガスとしてLNG4
0Nm3/Hと酸素200Nm3/Hが供給され、その高温火炎へ無機
質粉末原料としてのシリカ200kg/Hが溶射された。この
時球状化室温度は、850〜950℃を示しており、冷却室2
に吹きこまれた3000Nm3/Hの冷却空気により溶融化した
シリカの冷却がおこなわれ、球状化したシリカは、気送
管10を通して排出された。As standard operation, LNG4 as fuel gas to the thermal spray burner 3
0 Nm 3 / H and 200 Nm 3 / H of oxygen were supplied, and 200 kg / H of silica as an inorganic powder raw material was sprayed on the high temperature flame. At this time, the spheroidizing chamber temperature is 850 to 950 ° C, and the cooling chamber 2
The fused silica was cooled by 3000 Nm 3 / H of cooling air blown into the glass, and the spherical silica was discharged through a pneumatic tube 10.
例−1 上記基準操業において、シリカ溶射量を200kg/Hより280
kg/Hへ増加させた場合、ガラス化率82〜87%へ低下して
しまい封止剤として不十分なものとなった。そこで冷却
室2へ吹き込まれる冷却空気を3000Nm3/Hから900Nm3/H
まで減少させ、球状化室温度13を850〜900℃より1050〜
1100℃へ上昇させたところ、同一燃焼条件下で製品のガ
ラス化率94〜96%を維持しつつ、シリカ溶射量を240kg/
Hまで増大させる事ができた。Example-1 In the above standard operation, the silica spray amount was 280 from 200 kg / H.
When it was increased to kg / H, the vitrification rate decreased to 82-87%, making it insufficient as a sealant. 900Nm to where the cooling air blown into the cooling chamber 2 from 3000Nm 3 / H 3 / H
Spheroidizing chamber temperature 13 from 850 to 900 ℃ to 1050 to
When the temperature was raised to 1100 ° C, the silica spray amount was 240 kg / while maintaining the vitrification rate of 94-96% of the product under the same combustion conditions.
I was able to increase to H.
これは、従来の燃料LPG1Nm3当たりシリカ溶射量5kgを6k
gへ増大できた事となる。しかし、冷却室2出口ガス量
が減少し、出口ガス温度が350℃より800℃と高温となっ
たので、粒子分離処理の安定運転を継続するためサイク
ロン11の上流側に1500〜2000Nm3/Hの冷却空気を調節弁
7より補給した。This is a conventional fuel LPG 1Nm 3 silica spray amount 5kg 6k
It means that we could increase to g. However, since the outlet gas amount in the cooling chamber 2 decreased and the outlet gas temperature rose to a temperature as high as 350 ° C to 800 ° C, 1500 to 2000 Nm 3 / H upstream of the cyclone 11 in order to continue stable operation of the particle separation process. Cooling air was replenished from the control valve 7.
例−2 一方、シリカの溶射量を200kg/Hより120kg/Hへ40%減量
する場合、次の操業を行った第1段階:まずバーナー
への燃料ガス量の低減がおこなわれ、先に述べた安定操
業の限界燃焼負荷(75%)まで減量された。(この時の
LPGは40Nm3/Hより30Nm3/Hへ、酸素200Nm3/Hより150Nm3/
Hへ減少)、一方冷却空気は3000Nm3/Hより2200Nm3/Hへ
減量され、溶射量は200kg/Hより150kg/Hとなった。第
2段階:シリカの粗粒化を防止しつつさらに溶射量を12
0kg/Hまで減量するため、冷却室2への冷却空気量を220
0Nm3/Hより3100〜3300Nm3/Hした。その結果、球状化室
温度13は600〜700℃となり、製品の粗粒化比率を増大さ
せることなくガラス化率94〜97%の品質を維持すること
ができた。Example-2 On the other hand, when the thermal spraying amount of silica was reduced by 40% from 200 kg / H to 120 kg / H, the following operation was performed: The first stage: First, the fuel gas amount to the burner was reduced. It was reduced to the limit combustion load (75%) for stable operation. (At this time
LPG is to 30Nm 3 / H than 40Nm 3 / H, 150Nm than oxygen 200Nm 3 / H 3 /
Reduced to H), whereas the cooling air is reduced from 3000 Nm 3 / H 2200 nm to 3 / H, the sprayed amount became 150 kg / H than 200 kg / H. Second stage: further increase the spray amount by 12 while preventing coarsening of silica.
In order to reduce the amount to 0 kg / H, the cooling air volume to the cooling chamber 2 is set to 220
It was 3100-3300 Nm 3 / H from 0 Nm 3 / H. As a result, the spheroidizing chamber temperature 13 was 600 to 700 ℃, and the quality of vitrification rate of 94 to 97% could be maintained without increasing the coarsening ratio of the product.
以上の如く本発明によれば、品質の安定した球状粒子を
経済的に増減産できるものである。As described above, according to the present invention, it is possible to economically increase or decrease the production of spherical particles having stable quality.
第1図は、バーナーよりの距離と火炎温度及び球状化粒
子温度の関係を示す図、第2図は冷却空気流量と球状化
室周辺ガス温度及び冷却室出口ガス温度の関係を示す
図、第3図は、本発明の実施態様を示す装置例の説明図
である。 1……球状化室、2……冷却室 3……溶射バーナー、4……冷却空気ファン 5……ダストフィルター、6……冷却空気調節弁 7……サイクロン入口空気調節弁 8,9……粗粒子排出弁、10……気送管 11……サイクロン 12……粒子分離及びガス処理を行う下工程 13……球状化室温度計FIG. 1 is a diagram showing the relationship between the distance from the burner and the flame temperature and the spheroidizing particle temperature, and FIG. 2 is a diagram showing the relationship between the cooling air flow rate and the spheroidizing chamber surrounding gas temperature and the cooling chamber outlet gas temperature. FIG. 3 is an explanatory diagram of an example of a device showing an embodiment of the present invention. 1 ... Sphericalizing chamber, 2 ... Cooling chamber 3 ... Thermal spray burner, 4 ... Cooling air fan, 5 ... Dust filter, 6 ... Cooling air control valve, 7 ... Cyclone inlet air control valve, 8, 9 ... Coarse particle discharge valve, 10 ... pneumatic tube 11 ... cyclone 12 ... lower process for particle separation and gas treatment 13 ... spheroidizing chamber thermometer
Claims (1)
室で高温火炎と無機質粉末原料とを接触させて球状化処
理した後、冷却室内で冷却気体を供給して冷却する無機
質球状粒子の製造方法において、無機質粉末原料の供給
量に応じて冷却用気体の供給量を調整し、高温火炎温度
を制御することを特徴とする無機質球状粒子の製造方
法。1. An inorganic substance in which a high temperature flame and an inorganic powder raw material are brought into contact with each other in a spheroidizing chamber of a vertical furnace having a spheroidizing chamber and a cooling chamber to perform spheroidizing treatment, and then a cooling gas is supplied to cool the inorganic substance. In the method for producing spherical particles, the amount of cooling gas supplied is adjusted in accordance with the amount of the inorganic powder raw material supplied to control the high temperature flame temperature.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63259042A JPH0749100B2 (en) | 1988-10-14 | 1988-10-14 | Method for producing inorganic spherical particles |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63259042A JPH0749100B2 (en) | 1988-10-14 | 1988-10-14 | Method for producing inorganic spherical particles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02107516A JPH02107516A (en) | 1990-04-19 |
| JPH0749100B2 true JPH0749100B2 (en) | 1995-05-31 |
Family
ID=17328528
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63259042A Expired - Lifetime JPH0749100B2 (en) | 1988-10-14 | 1988-10-14 | Method for producing inorganic spherical particles |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0749100B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007034551A1 (en) * | 2005-09-22 | 2007-03-29 | Taiyo Nippon Sanso Corporation | Spheroidizig system and its operating method |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5308085B2 (en) * | 2008-07-08 | 2013-10-09 | 電気化学工業株式会社 | Method for producing spherical metal oxide powder |
| JP5469938B2 (en) * | 2009-07-10 | 2014-04-16 | 大陽日酸株式会社 | Manufacturing apparatus and manufacturing method of inorganic spheroidized particles |
| JP6221182B2 (en) * | 2014-10-27 | 2017-11-01 | 大陽日酸株式会社 | Inorganic spheroidized particle manufacturing apparatus and inorganic spheroidized particle manufacturing method |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62241541A (en) * | 1986-04-11 | 1987-10-22 | Nippon Steel Corp | Apparatus for producing and treating spheroidized inorganic particle |
-
1988
- 1988-10-14 JP JP63259042A patent/JPH0749100B2/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007034551A1 (en) * | 2005-09-22 | 2007-03-29 | Taiyo Nippon Sanso Corporation | Spheroidizig system and its operating method |
| JP4806681B2 (en) * | 2005-09-22 | 2011-11-02 | 大陽日酸株式会社 | Spheroidizing device and operation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02107516A (en) | 1990-04-19 |
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