JPS59102819A - Production of aluminum hydroxide having high whiteness - Google Patents
Production of aluminum hydroxide having high whitenessInfo
- Publication number
- JPS59102819A JPS59102819A JP57211005A JP21100582A JPS59102819A JP S59102819 A JPS59102819 A JP S59102819A JP 57211005 A JP57211005 A JP 57211005A JP 21100582 A JP21100582 A JP 21100582A JP S59102819 A JPS59102819 A JP S59102819A
- Authority
- JP
- Japan
- Prior art keywords
- aluminum hydroxide
- mud
- aluminate solution
- salt water
- bayer
- 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.)
- Granted
Links
Landscapes
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Abstract
Description
【発明の詳細な説明】
本発明・は高白色度水酸化アルミニウムの製造方法1こ
係り、詳しくは有機物等の着色物質を含有するアルミン
酸塩液力)らの高白色度水酸化アルミニウムの製造方法
)こ関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing aluminum hydroxide with high whiteness (1), specifically, production of aluminum hydroxide with high whiteness (aluminate liquid containing a coloring substance such as an organic substance). method).
周知の如くバイヤー法又はその改良法(以下バイヤー法
と称す)Iこよるアルミナの製造は、ボーキサイトを通
常180°C以上の温度の熱アルカリ溶液で処理し、ボ
ーキサイト中のアルミナ分を溶解抽出し、得られtこス
ラリーから酸化鉄、rイ酸塩、酸化チタン等の不溶解残
渣を赤泥としで分離し、不溶解残渣を分離した後の清澄
アルミン酸塩液に種子として水酸化アルミニウムを添加
し、通常50〜70′Cの温度範囲で水酸化アルミニウ
ムを分解析出せしめ、析出した水酸化アルミニウムをア
ルミン酸塩液から分離し、分離されtこ水酸化アルミニ
ウムの1部を種子として循環使用し、残余の水酸化アル
ミニウムを製品としで取り出し、池方分解後のアルミン
酸塩液はそのまま、または濃縮した後ボーキサイドの溶
解工程へ循環使用する工程より構成されている。As is well known, the production of alumina using the Bayer method or its modified method (hereinafter referred to as the Bayer method) involves treating bauxite with a hot alkaline solution, usually at a temperature of 180°C or higher, to dissolve and extract the alumina content in the bauxite. From the resulting slurry, undissolved residues such as iron oxide, chloride, titanium oxide, etc. are separated using red mud, and after the undissolved residues have been separated, aluminum hydroxide is added as a seed to the clarified aluminate solution. The precipitated aluminum hydroxide is separated from the aluminate solution, and a part of the separated aluminum hydroxide is recycled as a seed. The remaining aluminum hydroxide is removed as a product, and the aluminate solution after Ikegata decomposition is recycled to the boxide dissolution process either as is or after being concentrated.
ところで通常ボーキサイト中1こはフミン質物質を主体
とする有機物が含有されでおり、これらが溶解工程にお
いで熱アルカリ溶液に溶解又は可溶性塩となってアルミ
ン酸塩液中Iコf8 出する?、=め、また赤泥残渣を
母液から除く際に沈降剤とじて澱粉、合成高分子凝集剤
等が添加されるためlこバイヤ一工程のアルミン酸塩液
中tこ遂次有機物が蓄積されでくる。アルミン酸塩液中
の有機物の形態は高分子の錯体から最終分解生成物まで
種々の形で存在する。By the way, one part of bauxite usually contains organic substances mainly composed of humic substances, and in the dissolution process, these are dissolved in a hot alkaline solution or become soluble salts and released into the aluminate solution. Furthermore, when removing the red mud residue from the mother liquor, starch, synthetic polymer flocculants, etc. are added as precipitants, so organic matter is accumulated in the aluminate solution in the first step. It comes. The organic matter in the aluminate solution exists in various forms, from polymer complexes to final decomposition products.
こnらの有機物はアルミン酸塩液から水酸化アルミニウ
ムを分解析出する工程1こおいで、水酸化アルミニウム
と共沈しでくる。このため析出しrこ水酸化アルミニウ
ムは黄褐色に着色し、プラスチック、紙或は歯磨き用充
填材等の持1こ白色度の要求される用途lこは不向きと
なる。These organic substances co-precipitate with aluminum hydroxide in step 1 of separating and separating aluminum hydroxide from the aluminate solution. For this reason, the precipitated aluminum hydroxide is colored yellowish brown, making it unsuitable for applications that require high whiteness, such as plastics, paper, and toothpaste filling materials.
従前よりアルミン酸塩液中の着色物質を除去する方法が
種々提案され℃いるっ例えば活性炭により吸着除去する
方法、酸素、酸素含有物質で酸化処理する方法、更には
特開昭51−180698号公報1こ見られる如くキー
ゼリットを利用する方法、特開昭54−168799号
公報1こ見られる如<MgおよびCaの酸化物、水酸化
物、炭酸塩、硅・酸塩等を利用する方法等がある。Various methods have been proposed for removing colored substances from aluminate solutions, such as a method of adsorption and removal using activated carbon at ℃, a method of oxidation treatment with oxygen or an oxygen-containing substance, and a method of oxidation treatment with oxygen or an oxygen-containing substance, as well as Japanese Patent Application Laid-Open No. 180698/1983. There are methods using kieserite, as shown in 1, and methods using oxides, hydroxides, carbonates, silica salts, etc. of Mg and Ca, as shown in Japanese Patent Application Laid-open No. 54-168799. be.
これらの方法では高価な処理剤を使用するため処理費用
が嵩み、経済的でないという問題を包含する。These methods involve the problem that they are uneconomical because they use expensive processing agents, resulting in high processing costs.
ハ)たる状況下に鑑み本発明者らは簡便かつ廉価な処理
)こより高白色度の水酸化アルミニウムを取得すべく鋭
意研究を行なった結果、食塩電解工程よりの廃棄物であ
る塩水マッドを用いる場合1こは上記要ヰを満足し、高
白色度の水酸化アルミニウムが取得しうることを見い出
し、本発明を完成しtこ。c) In view of the current situation, the present inventors conducted intensive research to obtain aluminum hydroxide with a high brightness using a simple and inexpensive process. In case 1, we have discovered that it is possible to obtain aluminum hydroxide which satisfies the above requirements and has a high degree of whiteness, and has completed the present invention.
すなりち本発明は、バイヤー法におけるアルミン酸塩液
に塩水マッドを接触せしめ塩水マッドとの反応生成物を
分離除去しtコ後アルミン酸塩液より水酸化アルミニウ
ムを析出させることを特徴とする高白色度水酸化アルミ
ニウムの製造方法を提供するにある。The present invention is characterized by bringing a salt water mud into contact with an aluminate solution in the Bayer process, separating and removing a reaction product with the salt water mud, and precipitating aluminum hydroxide from the aluminate solution after t. The present invention provides a method for producing high whiteness aluminum hydroxide.
以下本発明方法を更tこ詳細に説明する。The method of the present invention will be explained in more detail below.
本発明方法の実施に当って使用する塩水マッドとは食塩
電解工業の塩水精製工程より分離除去されるゲル状残渣
であり、その組成は原料塩中に含有される不純物組成、
更には各具体的な不純物の除去方法により多少異なり、
一義的に定まるものではないが、通常炭酸カルシウム、
水酸化マグネシウム、硫酸カルシウム、硫酸バリウム等
の成分を包含しでいるものであればよく、就中少なくと
も塩水マッド(転体基準)を構成する物質の50重量%
が硫酸カルシウム、炭酸カルシウムおよび水酸化マグネ
シウムよりなりかつ、その組成が硫酸カルシウム30〜
60軍歌%、炭酸カルシウム10〜70重量%、水酸化
マグネシウム5〜20重量%より構成されるものが推奨
される。The salt water mud used in carrying out the method of the present invention is a gel-like residue separated and removed from the salt water purification process of the salt electrolysis industry, and its composition is composed of impurities contained in the raw salt,
Furthermore, it varies somewhat depending on the specific impurity removal method.
Although not uniquely determined, usually calcium carbonate,
It is sufficient that it contains components such as magnesium hydroxide, calcium sulfate, barium sulfate, etc., especially at least 50% by weight of the substances constituting the salt water mud (inversion basis).
is composed of calcium sulfate, calcium carbonate and magnesium hydroxide, and its composition is calcium sulfate 30~
It is recommended that the composition be composed of 60% military song, 10 to 70% by weight of calcium carbonate, and 5 to 20% by weight of magnesium hydroxide.
アルミン酸塩液を処理するため1こ添加される塩水マッ
ドの眼は転体基準で該液11に対しで0.059以上、
より好ましくは0.5〜30f/lの範囲で用いられる
。塩水マッドの添加量が0.05g/7+こ満たない場
合には取得される水酸化アルミニウムの白色度に与える
効果が顕著ではなく、801//lを越えで添加しCも
添加Jllこ見合う白色度の向上は見られない。The ratio of the salt water mud added to treat the aluminate solution is 0.059 or more for 11 of the solution based on the conversion standard.
More preferably, it is used in a range of 0.5 to 30 f/l. When the amount of salt water mud added is less than 0.05 g/7+, the effect on the whiteness of the obtained aluminum hydroxide is not significant, and when added in excess of 801//l, the whiteness commensurate with the addition of C. There is no improvement in the level.
本発明方法の実施1こおいで塩水マッドを添加し、処理
するアルミン酸塩液はアルミン酸塩液から水酸化アルミ
ニウムを分解析出する工程以前であればいずこでもよく
例えば、ボーキサイトとアルカリ溶液を混合加熱するア
ルミナ抽出工程、或は不溶解残渣を分離した後のアルミ
ン酸塩液であってもよく、アルミン酸塩液の温度も常温
から通常のバイヤー法1こおけるアルミナの抽出温度ま
で特に制限されるものではない。In step 1 of the method of the present invention, a salt water mud is added and the aluminate solution to be treated can be used anywhere before the step of separating and separating aluminum hydroxide from the aluminate solution. It may be an alumina extraction process that involves mixing and heating, or an aluminate solution after separating the insoluble residue, and the temperature of the aluminate solution is particularly limited from room temperature to the alumina extraction temperature in the usual Bayer process. It is not something that will be done.
尚、アルミン酸塩液と塩水マッドとの接触は攪拌しつつ
5分以上、好ましくは30分〜2時間実施すればよい。The aluminate solution and the salt water mud may be brought into contact with each other while stirring for 5 minutes or more, preferably 30 minutes to 2 hours.
かかる接触処理によりアルミン酸塩液中の着色物質はゲ
ル状沈澱物としで分離されるのでこれらを濾過分離して
除去した後常法により水酸化アルミニウムを分解析出せ
しめればよい。By this contact treatment, the colored substances in the aluminate solution are separated as gel-like precipitates, and after these are removed by filtration, aluminum hydroxide can be separated out by a conventional method.
本発明方法IこおいCゲル状沈澱物の濾過分離を考慮す
れば、不溶解残渣分離前のアルミナ抽出工程1こおいで
塩水マッドを加え、ゲル状沈澱物は赤泥と同時に分離除
去する方法が経済的である。Method I of the present invention Considering the filtration separation of the gelatinous precipitate, it is possible to add salt water mud in the first step of the alumina extraction step before separating the insoluble residue, and to separate and remove the gelatinous precipitate at the same time as the red mud. Economical.
以上詳述しtコ本発明方法jこよれば、食塩電解工業よ
り排出される廃棄物としての塩水マッドを有効利用し、
同等特別の付加的操作を必要とせず簡1fi+こしでか
つ廉価に白色度の優れた水酸化アルミニウムを取得しう
るものであり、その工業的価値は頗る大なるものである
。As detailed above, the method of the present invention effectively utilizes saltwater mud as waste discharged from the salt electrolysis industry,
It is possible to obtain aluminum hydroxide with excellent whiteness easily and inexpensively without requiring any special additional operations, and its industrial value is extremely great.
以下本発明方法を実施例1こよりさらに詳細1こ説明す
る。Hereinafter, the method of the present invention will be explained in more detail than in Example 1.
実施例l
Na20 1251/l でNa2O/Ad203(
モル比)魯
−1,6の組成を有し、有機物(有機質炭素として)2
01 、/ lを含む暗褐色のバイヤー液1こ塩水マッ
ド(CaS0487重量%、CaCO322重量%、M
f(OH)z 10重量%)を転体量基準で第1表1こ
示すごとく添加し、液温70゛Cで1時間攪拌を行ない
、沈殿物全濾過分離した。Example l Na20 1251/l Na2O/Ad203 (
molar ratio) has a composition of -1,6, and organic matter (as organic carbon) 2
01,/l of dark brown Bayer's solution 1 salt water mud (CaS0487 wt%, CaCO322 wt%, M
f(OH)z (10% by weight) was added as shown in Table 1 on the basis of the amount of converted material, stirred for 1 hour at a liquid temperature of 70°C, and the entire precipitate was separated by filtration.
このようにしで得た濾過液の色調を波長600nmの比
色計で光透過率を測定し、その結果を第1表Iこ示す。The color tone of the filtrate thus obtained was measured for light transmittance using a colorimeter with a wavelength of 600 nm, and the results are shown in Table I.
尚比較のため試薬グレードのCaCO3、Ca SO4
、Mf (OH)2及び塩水マッドの組成1こ相当する
混合試薬の調合剤を有機物の除去剤として用いtこ場合
の結果を合せて第1表1こ示す。For comparison, reagent grade CaCO3, CaSO4
, Mf (OH) 2 and a mixed reagent preparation corresponding to the composition of salt water mud were used as the organic matter removing agent.The results in this case are also shown in Table 1.
第 1 表
第1表から明らかび如く、本発明方法におい゛C使用す
る塩水マッドはCa5CJいCaCO3、My(OH)
2の試薬の島々単独添加の効果、更に塩水マットの組成
に相当する調合剤による添加効果の比較1こおいでも著
しい有機物の除去効果が達成される。Table 1 As is clear from Table 1, the salt water mud used in the method of the present invention is Ca5CJ, CaCO3, My(OH).
A comparison of the effect of adding the reagent islands alone in No. 2 and the effect of adding a preparation corresponding to the composition of the salt water mat.Even in the first case, a remarkable effect of removing organic matter was achieved.
実施例2
Na20 125y/# テNa20/A1203(モ
ル比) = 1.6の組成を有し、有機物(有機質炭素
として)20 f/11を含む暗褐色のバイヤー液に第
2表に示す添加剤を所要量添加し、液温220°Cで0
.5時間攪拌処理を行ない、生成したゲル状物質を炉渦
除去した。Example 2 The additives shown in Table 2 were added to a dark brown Bayer's liquid having a composition of Na20 125y/#te Na20/A1203 (molar ratio) = 1.6 and containing organic matter (as organic carbon) 20 f/11. Add the required amount of
.. Stirring treatment was carried out for 5 hours, and the gel-like substance produced was removed by vortexing in the furnace.
このようjこしで得tこバイヤー液の色調を実施例1と
同じ方法1こより測定し、結果を第2表に示す。但し塩
水マッドは実施例1と同じものである。The color tone of the Bayer liquid thus obtained by straining was measured using the same method as in Example 1, and the results are shown in Table 2. However, the salt water mud was the same as in Example 1.
第 2 表
実施例8
実施例2で用いたバイヤー液に第3表に示す組成の添加
剤を加え、液温220℃で0.5時間撹拌を行なった後
ゲル状物質を濾過除去しtこ。Table 2 Example 8 Additives having the composition shown in Table 3 were added to the Bayer liquid used in Example 2, and after stirring at a liquid temperature of 220°C for 0.5 hour, the gel-like substance was removed by filtration. .
このよう1こしで得たバイヤー液の色調を同様1こ測定
し、得られた結果を第3表1こ示す。The color tone of the Bayer's solution thus obtained was measured once in the same manner, and the results are shown in Table 3.
第 3 表Table 3
Claims (1)
を接触せしめ、塩水マッドとの反応生成物を分離除去し
た後アルミン酸塩液より水酸化アルミニウムを析出させ
ることを特徴とする高白色度水酸化アルミニウムの製造
方法。 2)アルミン酸塩液jこ対し塩水マッド(転体基準)を
0.05g/1以上添加する特許請求の範囲第1項記載
の方法 3)硫酸カルシウム、炭酸マグネシウム及び水酸化マグ
ネシウムの含有量が少なくとも全軍M(転体基準)の5
0重星形以上であってかつ、その組成が硫酸カルシウム
30〜60重量%、炭酸カルシウム10〜70M1に%
、水酸化マグネシウム5〜20重量%よりなる塩水マッ
ドを使用する特許請求の範囲第1項記載の方法。[Scope of Claims] 1) In the Bayer method, the aluminate solution is brought into contact with a salt water mud, and after separating and removing the reaction product with the salt water mud, aluminum hydroxide is precipitated from the aluminate solution. A method for producing high whiteness aluminum hydroxide. 2) The method according to claim 1, in which 0.05 g/1 or more of salt water mud (inversion basis) is added to the aluminate solution 3) The content of calcium sulfate, magnesium carbonate, and magnesium hydroxide is At least 5 of all forces M (transfer standard)
It has a zero double star shape or more, and its composition is 30 to 60% by weight of calcium sulfate and 10 to 70% of calcium carbonate.
2. A method according to claim 1, characterized in that a brine mud comprising 5 to 20% by weight of magnesium hydroxide is used.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57211005A JPS59102819A (en) | 1982-12-01 | 1982-12-01 | Production of aluminum hydroxide having high whiteness |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57211005A JPS59102819A (en) | 1982-12-01 | 1982-12-01 | Production of aluminum hydroxide having high whiteness |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59102819A true JPS59102819A (en) | 1984-06-14 |
JPH032802B2 JPH032802B2 (en) | 1991-01-17 |
Family
ID=16598744
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57211005A Granted JPS59102819A (en) | 1982-12-01 | 1982-12-01 | Production of aluminum hydroxide having high whiteness |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59102819A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4915930A (en) * | 1986-07-31 | 1990-04-10 | Aluminum Company Of America | Process for producing aluminum hydroxide of improved whiteness |
US5624646A (en) * | 1993-10-14 | 1997-04-29 | Aluminum Company Of America | Method for improving the brightness of aluminum hydroxide |
JP2010037188A (en) * | 2008-07-10 | 2010-02-18 | Sumitomo Chemical Co Ltd | Method for preparing decolored aqueous sodium aluminate solution |
CN102976570A (en) * | 2012-11-26 | 2013-03-20 | 中国铝业股份有限公司 | Method for reducing alkali consumption in Bayer production process |
-
1982
- 1982-12-01 JP JP57211005A patent/JPS59102819A/en active Granted
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4915930A (en) * | 1986-07-31 | 1990-04-10 | Aluminum Company Of America | Process for producing aluminum hydroxide of improved whiteness |
US5624646A (en) * | 1993-10-14 | 1997-04-29 | Aluminum Company Of America | Method for improving the brightness of aluminum hydroxide |
JP2010037188A (en) * | 2008-07-10 | 2010-02-18 | Sumitomo Chemical Co Ltd | Method for preparing decolored aqueous sodium aluminate solution |
CN102976570A (en) * | 2012-11-26 | 2013-03-20 | 中国铝业股份有限公司 | Method for reducing alkali consumption in Bayer production process |
Also Published As
Publication number | Publication date |
---|---|
JPH032802B2 (en) | 1991-01-17 |
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