JPS583969B2 - Alumina manufacturing method - Google Patents
Alumina manufacturing methodInfo
- Publication number
- JPS583969B2 JPS583969B2 JP55059904A JP5990480A JPS583969B2 JP S583969 B2 JPS583969 B2 JP S583969B2 JP 55059904 A JP55059904 A JP 55059904A JP 5990480 A JP5990480 A JP 5990480A JP S583969 B2 JPS583969 B2 JP S583969B2
- Authority
- JP
- Japan
- Prior art keywords
- solution
- alumina
- separated
- bauxite
- sodalite
- 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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- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Description
【発明の詳細な説明】
本発明は、ボーキサイトをアルミン酸ナトリウム溶液で
処理してアルミナを製造する、いわゆるバイヤー法にお
いて残渣として排出される赤泥を酸化鉄やチタニアのよ
うなアルカリ不溶の成分とソーダライト組成物のような
脱硅生成物とに分離する方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention is a method for treating bauxite with a sodium aluminate solution to produce alumina. The present invention relates to a method for separating desiliconization products such as sodalite compositions.
良く知られでいるように、バイヤー法において多量の赤
泥が排出されるが、現在の処では道路用材料などとして
僅かな量が利用されているに過ぎない。As is well known, a large amount of red mud is discharged in the Bayer process, but only a small amount is currently used as road material.
この理由は赤泥の脱水が困難なこと、取扱いが不便なこ
となどの他に、後出の表1に示す代表的な分析例から明
らかなように赤泥は種々の成分から成っており、何れの
成分の特徴も活かすことができないからである。The reason for this is that red mud is difficult to dehydrate and is inconvenient to handle.As is clear from the representative analysis examples shown in Table 1 below, red mud is composed of various components. This is because it is not possible to take advantage of the characteristics of any of the ingredients.
表1に示された赤泥成分のなかで、R−8102(粘土
型のシリカ)はアルカリ可溶であり、石英質のSiO2
(この量とR−8102量の合計がT一8102)、酸
化鉄および酸化チタンは実質的にアルカリ不溶である。Among the red mud components shown in Table 1, R-8102 (clay-type silica) is alkali-soluble, and quartz-based SiO2
(The sum of this amount and the amount of R-8102 is T-8102), iron oxide and titanium oxide are substantially insoluble in alkali.
従って赤泥をアルカリ可溶分とアルカリ不溶分に巧みに
分離できれば、前者は各種充填剤、軽量骨材、吸着剤な
どとしての応用面が開かれ、一方後者はセメントや製鉄
の副原料、顔料などとしで利用され易くなり、従来廃棄
に種種の問題を生じていた赤泥が有効に活用されること
になる。Therefore, if red mud could be skillfully separated into alkali-soluble and alkali-insoluble components, the former could be used as various fillers, lightweight aggregates, adsorbents, etc., while the latter could be used as an auxiliary raw material for cement and steel manufacturing, and as a pigment. Red mud, which previously had various problems when disposed of, will now be used effectively.
赤泥中の各種成分の分離は、排出後の赤泥を公知の方法
で適宜処理することによって容易に行なうことができる
が、このように別の工程で処理する方法は、経済性を考
慮すれば工業的実施は殆ど不可能なことは明らかである
。The various components in red mud can be easily separated by appropriately treating the discharged red mud using known methods. It is clear that industrial implementation is almost impossible.
一方、バイヤー法はアルカリ側で操業が行われるわけで
あるから、同法の工程の中に上記成分の分離を行なう工
程を巧みに組み込むことができれば、工業的にその分離
を行なうことができる筈である。On the other hand, since the Bayer process is operated on the alkaline side, if the process of separating the above components can be skillfully incorporated into the process of the process, it should be possible to perform the separation industrially. It is.
ボーキサイト中のSi02を予め除く方法としてR−S
iO2含有量の大きなボーキサイトを高温で焼成し、希
薄アルカリ液で溶出除去するLautawerk法が知
られているが、莫大な熱エネルギーと、アルミナの特定
抽出条件を必要とし、通常のボーキサイトに適用するこ
とは経済性から見て不可能である。R-S as a method to remove Si02 from bauxite in advance
The Lautawerk method is known, in which bauxite with a high iO2 content is calcined at high temperature and removed by elution with a dilute alkaline solution, but it requires a huge amount of thermal energy and specific extraction conditions for alumina, so it cannot be applied to ordinary bauxite. is impossible from an economic point of view.
バイヤー法において、ボーキサイトからのアルミナ抽出
液に対するR−8102の挙動は、次のようであること
が判っている。In the Bayer method, it has been found that the behavior of R-8102 with respect to alumina extract from bauxite is as follows.
すなわち、それは一旦アルミン酸ナトリウム溶液に溶出
するが、溶液中のシリカ濃度が一定値を超えるとソーダ
ライト等の核が発生して、これが種子効果を示し、シリ
カがソーダライトを主成分とする組成物として析出する
ようになる。That is, it is once eluted into a sodium aluminate solution, but when the silica concentration in the solution exceeds a certain value, nuclei such as sodalite are generated, which exhibits a seed effect, and the silica has a composition whose main component is sodalite. It begins to precipitate as a substance.
R−8102のアルミン酸ナトリウム溶液に対する溶解
速度はアルミナと同様であって、抽出液の温度、ソーダ
濃度およびNa20/Al203モル比(以下単にモル
比と称する)が高い程、大きくなるが溶解したR−81
02がソーダライト化合物となって析出する臨界濃度は
、抽出液の温度が低い程、ソーダ濃度が高い程、そして
モル比が低い程高くなり、このような条件では析出速度
も小さくなる。The dissolution rate of R-8102 in a sodium aluminate solution is similar to that of alumina, and the higher the extract temperature, soda concentration, and Na20/Al203 molar ratio (hereinafter simply referred to as molar ratio), the higher the dissolution rate of R-8102, but the rate of dissolution of R-8102 in a sodium aluminate solution increases. -81
The critical concentration at which 02 becomes a sodalite compound and precipitates becomes higher as the temperature of the extract is lower, the soda concentration is higher, and the molar ratio is lower, and under these conditions, the precipitation rate also becomes lower.
従って、原理的にはR−SiO2が溶解するが析出しな
い条件でボーキサイトを抽出液で処理した後濾過し(こ
の工程を以後R−8102溶出工程と称する)、濾滓を
通常のバイヤ一工程へ、また濾液に必要に応じて種子を
添加して溶解しているR一Si02をソーダライト等の
組成物として析出せしめたのち、濾過し(この工程を以
後R−8102析出工程と称し、上記工程と合わせた全
工程を脱硅工程と称する)、濾液を、このプロセスに循
環するようにすれば、R−Si02成分の分離が行われ
るようになる。Therefore, in principle, bauxite is treated with an extract under conditions where R-SiO2 dissolves but does not precipitate, and then filtered (this step is hereinafter referred to as the R-8102 elution step), and the filter cake is sent to the usual Bayer step. In addition, seeds are added to the filtrate as necessary to precipitate the dissolved R-Si02 as a composition such as sodalite, and then filtered (this step is hereinafter referred to as the R-8102 precipitation step, and the above steps are performed). (The entire process including this is called a desiliconization process).If the filtrate is circulated through this process, the R-Si02 component can be separated.
然しなから、このようなプロセスにおいて、R−SiO
2溶出工程でR−8102の析出を避けるためには、例
えば抽出液のソーダ濃度を高くするか、あるいは大量の
抽出液を用いるようにしなければならず、そうなると、
R−SiO2析出工程でのR−Si02の析出が困難と
なる。However, in such a process, R-SiO
2. In order to avoid precipitation of R-8102 in the elution step, it is necessary, for example, to increase the soda concentration of the extract or use a large amount of extract.
Precipitation of R-Si02 in the R-SiO2 precipitation step becomes difficult.
また、このようなピロセスをバイヤ一工程の前工程とし
で組み入れ、その工程内でアルカリ溶液を循環せしめる
と、この工程内の循環液はアルミナで直ちに飽和するの
で、最早ボーキサイト中のアルミナを溶解しなくなり、
その結果ボーキサイト粒子が崩壊しなくなってR−Si
02の溶解量も低下するので、この工程のなかに循環液
からアルミナを抜く工程が必要となって来る。In addition, if such a pyrocess is incorporated as a pre-process of the Bayer 1 process and an alkaline solution is circulated in that process, the circulating liquid in this process will immediately become saturated with alumina, and the alumina in the bauxite will no longer be dissolved. gone,
As a result, bauxite particles no longer disintegrate and R-Si
Since the amount of 02 dissolved also decreases, a step for removing alumina from the circulating fluid becomes necessary during this step.
上記したように、バイヤ一工程を利用して赤泥をR−S
i02含有物とアルカリ不溶性物の二種に分離すること
は実際面で多くの困難があり、従来は工業規模で実施さ
れでいない。As mentioned above, red mud is made into R-S using the Buyer step.
There are many practical difficulties in separating the i02-containing material and the alkali-insoluble material, and it has not been carried out on an industrial scale so far.
本発明は、通常のバイヤー法において排出される赤泥を
、通常のアルミナ生産能率を維持しつつ、アルカリ可溶
部分とアルカリ不溶部分に効果的に分離することを目的
としたものであって、通常のバイヤー法の工程の前段に
脱硅工程を設け、この工程をアルミナ抽出工程と有機的
に結びつけ、赤泥成分の分別とアルミナの抽出とを同時
に行なうことを、その要旨とするものである。The present invention aims to effectively separate red mud discharged in the normal Bayer process into an alkali-soluble portion and an alkali-insoluble portion while maintaining normal alumina production efficiency. The gist of this method is to provide a desiliconization process before the normal Bayer process, organically link this process with the alumina extraction process, and simultaneously perform the separation of red mud components and the extraction of alumina. .
すなわち、本発明方法は、ボーキサイトをアルミン酸ナ
トリウム溶液(以下単に溶液という)で処理して不溶解
残渣を赤泥としで排出し、一方赤泥を分離した溶液から
水酸化アルミニウムを析出せしめ、これを焼成してアル
ミナとし、水酸化アルミニウム分離後の溶液を循環使用
する、いわゆるバイヤー法において、ボーキサイトを溶
液で処理してアルカリ可溶性シリカを溶出せしめ、溶出
したシリカをソーダライト組成物として析出分離する脱
硅工程と、該脱硅処理されたボーキサイトを溶液で処理
してアルミナを抽出する主工程を設け、主工程の水酸化
アルミニウムを分離した溶液と、脱硅工程の析出したソ
ーダライト組成物を分離した溶液の少なくとも一部との
混合溶液を脱硅工程用の溶液とし、残余の溶液を主工程
用の溶液とすることを特徴とするものである。That is, in the method of the present invention, bauxite is treated with a sodium aluminate solution (hereinafter simply referred to as a solution), the insoluble residue is discharged as red mud, and aluminum hydroxide is precipitated from the solution from which the red mud is separated. In the so-called Bayer process, in which alumina is calcined and the solution after separating aluminum hydroxide is recycled, bauxite is treated with a solution to elute alkali-soluble silica, and the eluted silica is precipitated and separated as a sodalite composition. A desiliconization process and a main process of treating the desiliconized bauxite with a solution to extract alumina are provided, and the solution from which aluminum hydroxide is separated in the main process and the sodalite composition precipitated in the desiliconization process are combined. A mixed solution with at least a part of the separated solution is used as a solution for the desiliconization process, and the remaining solution is used as a solution for the main process.
本発明方法を、回分方式の実施態様に基づいて詳細に説
明するが、連続方式による実施も可能であることは言う
までもない。Although the method of the present invention will be explained in detail based on a batch method, it goes without saying that it can also be implemented in a continuous method.
第1図は、本発明方法の一つの実施態様を示した概略の
工程図で、左側の系が脱硅工程、そして右側の系が主工
程である。FIG. 1 is a schematic process diagram showing one embodiment of the method of the present invention, in which the system on the left is the desiliconization process and the system on the right is the main process.
ボーキサイトAは、R−SiO2溶出槽1において、R
−Si02溶出処理を受けた後、濾過機2によって濾液
と濾滓(すなわち脱硅されたボーキサイト)に分離され
る。In the R-SiO2 elution tank 1, bauxite A is
-After undergoing the Si02 elution treatment, the filter is separated into a filtrate and a filter cake (i.e., desiliconized bauxite) by a filter 2.
濾液は次のR−8102析出槽3に送られ、必要に応じ
てソーダライト種子が添加されて溶存しているシリカが
ソーダライト組成物として析出する。The filtrate is sent to the next R-8102 precipitation tank 3, and if necessary, sodalite seeds are added to precipitate the dissolved silica as a sodalite composition.
析出が終った液は濾過機4によってソーダライト組成物
Bと濾液に分離され、濾液は一部を分岐され、残余は貯
槽12に入れられる。The liquid after precipitation is separated into sodalite composition B and a filtrate by a filter 4, a part of the filtrate is branched off, and the remainder is put into a storage tank 12.
脱硅されたボーキサイトは、通常のバイヤー法と全く同
様に処理される。The desiliconized bauxite is processed in exactly the same way as the normal Bayer process.
すなわち、蒸煮缶5においてアルミナ溶出処理を受けた
後、シックナー6によって鉄分含有量の高い残渣を含む
泥漿とアルミナ含有量の高い溶液とに分けられる。That is, after being subjected to alumina elution treatment in the steamer 5, it is separated by the thickener 6 into a slurry containing a residue with a high iron content and a solution with a high alumina content.
前者は濾過機7において、鉄分含有量の高い残渣C(従
来の赤泥よりもシリカ分の少ないもの)と濾液に分離さ
れるが、濾液はそのなかの微粒子の回収のため、シツク
ナー6に循環される。The former is separated into a residue C with a high iron content (lower silica content than conventional red mud) and a filtrate in a filter 7, but the filtrate is circulated to a thickener 6 to collect fine particles therein. be done.
アルミナ含有量の高い溶液は、水酸化アルミニウム析出
槽8において、水酸化アルミニウム種子が添加されで、
溶存しているアルミナ分が水酸化アルミニウムとして析
出する。The solution with a high alumina content is prepared by adding aluminum hydroxide seeds in an aluminum hydroxide precipitation tank 8.
Dissolved alumina precipitates as aluminum hydroxide.
析出が終った液はシックナ−9において水酸化アルミニ
ウムを含む泥漿と清澄液に分けられ、前者は濾過機10
によって濾過された後、水酸化アルミニウムはロータリ
ーキルン11によって焼成されてアルミナDとなり、後
者は必要に応じて蒸発濃縮(図示せず)などの処理を受
けた後、貯槽12に入れられる。After the precipitation, the liquid is separated into slurry containing aluminum hydroxide and clear liquid in the thickener 9, and the former is passed through the filter 10.
After filtering, the aluminum hydroxide is fired in a rotary kiln 11 to become alumina D, and the latter is placed in a storage tank 12 after being subjected to treatments such as evaporation and concentration (not shown) as required.
この実施態様において、溶液は次のように循環利用され
る。In this embodiment, the solution is recycled as follows.
すなわち、脱硅工程における濾過機4の濾液(以下脱硅
工程終了液という)の一部は、主工程用の溶液として用
いられ、残余の脱硅工程終了液は、主工程におけるシツ
クナー9の清澄液(以下主工程終了液という)と混合さ
れて脱硅工程用の溶液としで用いられる。That is, a part of the filtrate of the filter 4 in the desiliconization process (hereinafter referred to as the desiliconization process finished liquid) is used as a solution for the main process, and the remaining desiliconization process finished liquid is used for clarification of the thickener 9 in the main process. It is mixed with a liquid (hereinafter referred to as the main process finished liquid) and used as a solution for the desiliconization process.
このような循環利用の仕方をすることによって、脱硅工
程において望ましいモル比を持った溶液を得ることがで
きると共に、脱硅工程でシリヵと同時に溶出したアルミ
ナ分は、主工程におけるアルミナ生産に有効に利用され
るという利点が得られる。By recycling in this way, it is possible to obtain a solution with a desired molar ratio in the desiliconization process, and the alumina that is eluted together with silica in the desiliconization process is effective for alumina production in the main process. This has the advantage of being used for
第2図は、もう一つの実施態様を示したものである。FIG. 2 shows another embodiment.
本態様は、上記第1図に示した実施態様と溶液の循環方
法が異なるのみであるから、工程の説明は省略する。This embodiment differs from the embodiment shown in FIG. 1 above only in the solution circulation method, so a description of the steps will be omitted.
本態様においては、脱硅工程終了液と主工程終了液は貯
槽12において混合され、その一部が主工程用に、また
残余が脱硅工程用に用いられる。In this embodiment, the desiliconization process finished liquid and the main process finished liquid are mixed in the storage tank 12, a part of which is used for the main process and the remainder used for the desiliconization process.
この方法は、溶液の循環操業が容易になるという利点が
あるが、脱硅工程の操業の自由度が減ずるという欠点も
あるので、これを回避するためには脱硅工程終了液の一
部を抜き出して、それを主工程用溶液に加えるようにす
ればよい。This method has the advantage of making it easier to circulate the solution, but it also has the disadvantage of reducing the degree of freedom in the operation of the desiliconization process. All you have to do is extract it and add it to the main process solution.
このような方法を採れば、第1図における方法と同様の
効果を挙げることができることは明らかである。It is clear that if such a method is adopted, the same effect as the method shown in FIG. 1 can be achieved.
以上述べたことから判るように本発明方法によるときは
、通常の赤泥をソーダライト組成物と鉄分含有量の高い
成分とに容易に分離し得るのみならず、バイヤ一工程に
付加する設備は簡単であって、しかもアルミナ生産能率
には何等影響を与えないという効果を挙げることができ
る。As can be seen from the above, when using the method of the present invention, not only can ordinary red mud be easily separated into a sodalite composition and a component with a high iron content, but also the equipment added to the bayer step can be easily separated. It is simple and has the advantage of not affecting the alumina production efficiency in any way.
本発明方法における脱硅工程の好ましい操業条件は、次
のようである。Preferred operating conditions for the desiliconization step in the method of the present invention are as follows.
1.R−8102溶出条件
(1)后液
Na20濃度 90〜200g/INa20/A
1203モル比 2.0 〜4.0(2)溶液とボーキ
サイトの比 5〜30m3/t(3)反応温度
60〜110℃(4)反応時間
0.5〜10hr2,ソーダライト組成物析出条件
(1)温度 90〜2oo℃(2)反
応時間 0.1〜1ohr上記において
、溶液のモル比および溶液/ボーキサイトの比は、それ
ぞれ大きい程好ましいが、あまり大きくすると工程全体
のバランスが取り難くなるので、生産するアルミナの品
種または生産能率を考慮して、上記範囲で適宜決めれば
よい。1. R-8102 elution conditions (1) Eluate Na20 concentration 90-200g/INa20/A
1203 Molar ratio 2.0 to 4.0 (2) Ratio of solution to bauxite 5 to 30 m3/t (3) Reaction temperature
60-110℃ (4) Reaction time
0.5-10hr2, Sodalite composition precipitation conditions (1) Temperature 90-2oooC (2) Reaction time 0.1-1ohr In the above, the molar ratio of the solution and the ratio of solution/bauxite are preferably as large as possible. If it is too large, it becomes difficult to balance the entire process, so it may be determined as appropriate within the above range, taking into account the type of alumina to be produced or the production efficiency.
なお、本発明方法において、ボーキサイト中のR−Si
02の一部は未溶解のまま主工程へ入り、蒸煮缶の中で
アルミナと共に溶出するが、シリヵ濃度が低いためソー
ダライト組成物としては析出し難いので、この一部は水
酸化アルミニウムと共に析出して製品アルミナを汚染す
ることもある。In addition, in the method of the present invention, R-Si in bauxite
A part of 02 enters the main process undissolved and is eluted with alumina in the steamer, but because the silica concentration is low, it is difficult to precipitate as a sodalite composition, so this part precipitates with aluminum hydroxide. and contaminate the product alumina.
このようなシリカ分を除く必要がある場合には、主工程
の前において、脱硅されたボーキサイトに溶液を加え、
例えば泥漿濃度6oog/1、Na20濃度130g/
l1温度90〜140℃の条件で1〜20hr処理すれ
ば、未溶解のR−Si02は溶解し、ついで、ソーダラ
イト組成物として析出し、これは蒸煮によっても溶解し
ないので、鉄分含有量の高い赤泥とともに排出される。If it is necessary to remove such silica, add a solution to the desiliconized bauxite before the main process.
For example, slurry concentration 6oog/1, Na20 concentration 130g/1
If treated for 1 to 20 hours at a l1 temperature of 90 to 140°C, undissolved R-Si02 will be dissolved and then precipitated as a sodalite composition, which will not dissolve even by steaming, so it will not dissolve even by steaming. It is discharged along with red mud.
以下に本発明方法を回分方式で実施した例を示す。An example in which the method of the present invention was carried out in a batch manner will be shown below.
実施例1
三水和物型ボーキサイト(シーバ鉱)を用い、第1図に
示された工程図に従ってアルミナ生産(但し水酸化アル
ミニウムの焼成は不実施)を行なった。Example 1 Alumina was produced using trihydrate bauxite (sheba ore) according to the process diagram shown in FIG. 1 (however, calcination of aluminum hydroxide was not performed).
9メッシュ以下に紛砕したボーキサイト2tをR−81
02溶出槽に入れ、これにNa20:135、g/x、
モル比2.40の溶液28m3を加えて100℃で2h
r処理し、直ちに加圧葉状濾過機を用いて濾過して、脱
硅ボーキサイト濾液に分離した。R-81 2 tons of bauxite crushed to 9 mesh or less
02 elution tank, and add Na20:135, g/x,
Add 28 m3 of a solution with a molar ratio of 2.40 and heat at 100°C for 2 hours.
Immediately after filtration using a pressurized leaf filter, the product was separated into a desiliconized bauxite filtrate.
モル比2.0となった濾液28m3をR−Si02析出
槽に送り、350メッシュ以下のソーダライト種,子2
00kgを添加しで、140℃でlhr処理したのち、
加圧葉状濾過機で濾過して、ソーダライト組成物正味(
種子添加量を除いた量。28 m3 of the filtrate with a molar ratio of 2.0 was sent to the R-Si02 precipitation tank, and sodalite seeds with a size of 350 mesh or less were added.
After adding 00 kg and performing lhr treatment at 140°C,
Filtered with a pressurized leaf filter to obtain a net sodalite composition (
Amount excluding the amount of seeds added.
以下同じ)152k9を得た。Same hereafter) Obtained 152k9.
この濾液(モル比2.00)28m’のうち14m’.
を主工程に分岐し、脱硅処理されたボーキサイトととも
に蒸煮缶において150℃でlhr処理し、シツクナー
および真空回転型濾過機によってモル比1.50の濾液
と高鉄分の赤泥とに分離した。Of this filtrate (molar ratio 2.00) 28 m', 14 m'.
The mixture was branched into the main process, treated with lhr at 150°C in a steamer together with the desiliconized bauxite, and separated into a filtrate with a molar ratio of 1.50 and red mud with a high iron content using a thickener and a vacuum rotary filter.
上記濾液を析出槽に入れ、これに150メツシユ以下の
水酸化アルミニウム種子1,400kgを添加し、60
℃から50℃まで自然冷却させながら、48hr析出処
理を行なった。The above filtrate was put into a precipitation tank, and 1,400 kg of aluminum hydroxide seeds of 150 mesh or less were added thereto.
The precipitation treatment was carried out for 48 hours while allowing natural cooling from .degree. C. to 50.degree.
析出終了後シツクナーおよび真空回転型濾過機によって
、モル比3.00の濾液14m3と水酸化アルミニウム
正味1,506kg(アルミナ換算985kg)に分離
した。After the precipitation was completed, the mixture was separated into 14 m3 of filtrate with a molar ratio of 3.00 and a net weight of 1,506 kg of aluminum hydroxide (985 kg in terms of alumina) using a thickener and a vacuum rotary filter.
シツクナーから得られた濾液吉、脱硅工程終了液の残り
(モル比2.00)14m3を貯槽において混合し、モ
ル比2、40の溶液28m3を得た。The filtrate obtained from the thickener and 14 m3 of the remaining liquid after the desiliconization process (molar ratio 2.00) were mixed in a storage tank to obtain 28 m3 of a solution with a molar ratio of 2.40.
(脱硅工程用の溶液となる)
本実施例においで得られた高鉄分赤泥の組成を表1に、
ソーダライト組成物の組成を表2に、それぞれ示す。The composition of the high-iron red mud obtained in this example (which becomes a solution for the desiliconization process) is shown in Table 1.
The compositions of the sodalite compositions are shown in Table 2.
実施例2
実施例1と同じボーキサイトを用い、第2図に示された
工程図に従ってアルミナ生産(但し水酸化アルミニウム
の焼成は不実施)を行なった。Example 2 Using the same bauxite as in Example 1, alumina production was carried out according to the process diagram shown in FIG. 2 (however, calcination of aluminum hydroxide was not performed).
9メッシュ以下に粉砕したボーキサイト2tをR−Si
O2溶出槽に入れ、これにモル比2.25の溶液28m
3を加えてIQO℃で2hr処理し、直ちに加圧葉状濾
過機を用いて濾過して、脱硅ボーキサイトと濾液に分離
した。2 tons of bauxite crushed to 9 mesh or less is made into R-Si
Put it in an O2 elution tank and add 28ml of a solution with a molar ratio of 2.25 to it.
3 was added thereto and treated at IQO°C for 2 hours, and immediately filtered using a pressurized leaf filter to separate the desiliconized bauxite and the filtrate.
モル比2.00となった濾液28m3をR−8102析
出槽に送り、350メッシュ以下のソーダライト種子2
00kgを添加して140℃でlhr処理した後、加圧
葉状濾過機で濾過して、ソーダライト組成物正味144
k9を得た。28 m3 of the filtrate with a molar ratio of 2.00 was sent to the R-8102 precipitation tank, and 2 sodalite seeds of 350 mesh or less were sent to the R-8102 precipitation tank.
00 kg was added and subjected to lhr treatment at 140°C, and then filtered with a pressurized leaf filter to obtain a sodalite composition net of 144 kg.
I got k9.
この溶液(モル比2.00)28mとモル比3.DOの
主工程終了液14m3を貯槽において混合し、モル比2
.25の溶液42m゜を得た。28 m of this solution (molar ratio 2.00) and molar ratio 3. 14 m3 of DO main process finished liquid was mixed in a storage tank, and the molar ratio was 2.
.. A 42 mm solution of No. 25 was obtained.
該溶液のうち、脱硅工程に用いた残りの14m3を脱硅
ボーキサイトとともに蒸煮缶に入れ、140℃でlhr
処理した後、シツクナーおよび真空回転型濾過機によっ
て、モル比1.50の濾液と高鉄分の赤泥とに分離した
。The remaining 14 m3 of the solution used in the desiliconization process was put into a steamer together with the desiliconized bauxite, and heated at 140°C for lhr.
After treatment, it was separated into a filtrate with a molar ratio of 1.50 and a red mud with a high iron content using a thickener and a vacuum rotary filter.
上記濾液を析出槽に入れ、これに150メッシュ以下の
水酸化アルミニウム種子L400kgを添加し、60℃
から50℃まで自然冷却させながら、48hr析出処理
を行なった。The above filtrate was put into a precipitation tank, 400 kg of aluminum hydroxide seeds L of 150 mesh or less were added thereto, and the mixture was heated to 60°C.
The precipitation treatment was carried out for 48 hours while cooling naturally from to 50°C.
析出終了後、シツクナーおよび真空回転型濾過機によっ
て、モル比3.00の濾液14m3と、水酸化アルミニ
ウム正味1,502kg(アルミナ換算982kg)に
分離した。After the precipitation, the mixture was separated into 14 m3 of filtrate with a molar ratio of 3.00 and 1,502 kg of aluminum hydroxide (982 kg in terms of alumina) using a thickener and a vacuum rotary filter.
本実施例によって得られた高鉄分赤泥の組成を表1に、
またソーダライト組成物の組成を表2にそれぞれ示す。The composition of the high iron content red mud obtained in this example is shown in Table 1.
Further, the compositions of the sodalite compositions are shown in Table 2.
以上の実施例から判るように本発明方法によれば、従来
のバイヤ一工程に簡単な設備を付加するだけで、いわゆ
る赤泥をソーダライト組成物と鉄分含有量の多い成分に
容易に分離することができ、しかも実施例において得ら
れた正味の水酸化アルミニウム析出量のボーキサイト量
に対する比は、通常のバイヤー法のそれとほぼ同じであ
るから、生産性においても問題のないことは明らかであ
る。As can be seen from the above examples, according to the method of the present invention, so-called red mud can be easily separated into a sodalite composition and a component with a high iron content by simply adding simple equipment to the conventional buyer process. Moreover, since the ratio of the net amount of aluminum hydroxide precipitated to the amount of bauxite obtained in the examples is almost the same as that of the usual Bayer method, it is clear that there is no problem in terms of productivity.
第1図および第2図は、それぞれ本発明方法の実施態様
を示す概略の工程図である。
図中、l:R−Sin2溶出槽、3:R−SIO2析出
槽、5:蒸煮缶、8:水酸化アルミニウム析出槽をそれ
ぞれ示す。FIG. 1 and FIG. 2 are schematic process diagrams each showing an embodiment of the method of the present invention. In the figure, 1: R-Sin2 elution tank, 3: R-SIO2 precipitation tank, 5: steaming can, 8: aluminum hydroxide precipitation tank, respectively.
Claims (1)
て不溶解残渣を赤泥として排出し、一方赤泥を分離した
溶液から水酸化アルミニウムを析出せしめ、これを焼成
してアルミナを製造する方法において、 ボーキサイトをアルミン酸ナトリウム溶液で処理しで、
アルカリ可溶性シリカを溶出せしめ、溶出したシリカを
ソーダライト組成物として析出分離する脱硅工程と、脱
硅処理されたボーキサイトをアルミン酸ナトリウム溶液
で処理してアルミナを抽出する主工程とを設け、主工程
の析出した水酸化アルミニウムを分離した溶液と、脱硅
工程の析出したソーダライト組成物を分離した溶液の少
なくとも一部との混合溶液を脱硅工程用の溶液とし、残
余の溶液を主工程用の溶液とすることを特徴とするアル
ミナ製造法。 2 主工程の析出した水酸化アルミニウムを分離した溶
液と、脱硅工程の析出したソーダライト組成物を分離し
た溶液の一部との混合溶液を脱硅工程用の溶液とし、後
者の残余の溶液を主工程用の溶液とすることを特徴とす
る特許請求の範囲第1項記載のアルミナ製造法。 3 主工程の析出した水酸化アルミニウムを分離した溶
液と脱硅工程の析出したソーダライト組成物を分離した
溶液とを混合し、その一部を脱硅工程用の、また残余を
主工程用の溶液とすることを特徴とする特許請求の範囲
第1項記載のアルミナ製造法。[Claims] 1. Treating bauxite with a sodium aluminate solution and discharging the undissolved residue as red mud, while precipitating aluminum hydroxide from the solution from which the red mud was separated, and baking this to produce alumina. In the method, bauxite is treated with a sodium aluminate solution,
The main process consists of a desiliconization process in which alkali-soluble silica is eluted and the eluted silica is precipitated and separated as a sodalite composition, and a main process in which the desiliconized bauxite is treated with a sodium aluminate solution to extract alumina. A mixed solution of at least a portion of the solution from which aluminum hydroxide precipitated in the process was separated and the solution from which the precipitated sodalite composition was separated from the desiliconization process is used as the solution for the desiliconization process, and the remaining solution is used in the main process. An alumina manufacturing method characterized by making it into a solution for use. 2 A mixed solution of the solution from which precipitated aluminum hydroxide was separated in the main process and a part of the solution from which the precipitated sodalite composition was separated from the desiliconization process was used as the solution for the desiliconization process, and the remaining solution from the latter was used as the solution for the desiliconization process. 2. The alumina manufacturing method according to claim 1, wherein the alumina is used as a solution for the main process. 3. Mix the solution in which precipitated aluminum hydroxide in the main process was separated and the solution in which the precipitated sodalite composition in the desiliconization process was separated, and use a portion of the solution for the desiliconization process and the remainder for the main process. 2. The method for producing alumina according to claim 1, wherein the alumina production method is made into a solution.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55059904A JPS583969B2 (en) | 1980-05-08 | 1980-05-08 | Alumina manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55059904A JPS583969B2 (en) | 1980-05-08 | 1980-05-08 | Alumina manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56160321A JPS56160321A (en) | 1981-12-10 |
| JPS583969B2 true JPS583969B2 (en) | 1983-01-24 |
Family
ID=13126570
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55059904A Expired JPS583969B2 (en) | 1980-05-08 | 1980-05-08 | Alumina manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS583969B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993020251A1 (en) * | 1992-04-03 | 1993-10-14 | Sumitomo Chemical Company, Limited | Process for producing iron-making material composition comprising bauxite dissolution residue |
| CN105217903A (en) * | 2014-06-26 | 2016-01-06 | 沈阳铝镁设计研究院有限公司 | A kind of equipment configuration method of red-mud settlement and separation washing procedure |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102600791A (en) * | 2012-04-01 | 2012-07-25 | 昆明理工大学 | Granular red mud absorbent and preparation method thereof |
-
1980
- 1980-05-08 JP JP55059904A patent/JPS583969B2/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993020251A1 (en) * | 1992-04-03 | 1993-10-14 | Sumitomo Chemical Company, Limited | Process for producing iron-making material composition comprising bauxite dissolution residue |
| CN105217903A (en) * | 2014-06-26 | 2016-01-06 | 沈阳铝镁设计研究院有限公司 | A kind of equipment configuration method of red-mud settlement and separation washing procedure |
| CN105217903B (en) * | 2014-06-26 | 2017-11-10 | 沈阳铝镁设计研究院有限公司 | A kind of equipment configuration method of red- mud settlement and separation washing procedure |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56160321A (en) | 1981-12-10 |
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