JPH05279018A - Production of magnesium hydroxide - Google Patents

Production of magnesium hydroxide

Info

Publication number
JPH05279018A
JPH05279018A JP10178592A JP10178592A JPH05279018A JP H05279018 A JPH05279018 A JP H05279018A JP 10178592 A JP10178592 A JP 10178592A JP 10178592 A JP10178592 A JP 10178592A JP H05279018 A JPH05279018 A JP H05279018A
Authority
JP
Japan
Prior art keywords
digestion reaction
magnesium oxide
digestion
reaction
magnesium hydroxide
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
Application number
JP10178592A
Other languages
Japanese (ja)
Inventor
Kenichi Nakagawa
健一 中川
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP10178592A priority Critical patent/JPH05279018A/en
Publication of JPH05279018A publication Critical patent/JPH05279018A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F5/00Compounds of magnesium
    • C01F5/14Magnesium hydroxide
    • C01F5/16Magnesium hydroxide by treating magnesia, e.g. calcined dolomite, with water or solutions of salts not containing magnesium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

Abstract

PURPOSE:To improve the digestion reaction property, shorten the reaction time, and enhance the reaction rate by improving the digestion method, in a production of magnesium hydroxide by a digestion reaction of calcined magnesium oxide. CONSTITUTION:In a digestion reaction reactor 1, the digestion of the calcined magnesium oxide and water is performed. Also while a magnesium hydroxide layer which is formed on a particle of the calcined magnesium oxide is ground with a surface pulverizing means 2, the digestion reaction is advanced.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は、排液の中和剤や排煙
脱硫用のアルカリ剤などとして有用な水酸化マグネシウ
ムの製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing magnesium hydroxide which is useful as a neutralizing agent for effluent and an alkaline agent for flue gas desulfurization.

【0002】[0002]

【従来の技術】水酸化マグネシウムの製造方法のひとつ
に、マグネサイトなどの炭酸マグネシウム鉱石を比較的
低温でか焼したのち、粗砕機(ハンマ―クラツシヤ)や
微粉砕機(レイモンドミル)などで通常100μm以下
の粒子径に乾式粉砕して得られる、いわゆる軽焼酸化マ
グネシウムを、水で消化反応させる方法がある。
2. Description of the Related Art As one of the methods for producing magnesium hydroxide, after calcining magnesium carbonate ore such as magnesite at a relatively low temperature, it is usually used with a crusher (hammer-crusher) or a fine crusher (Raymond mill). There is a method of subjecting so-called light-burned magnesium oxide obtained by dry pulverization to a particle size of 100 μm or less to a digestion reaction with water.

【0003】[0003]

【発明が解決しようとする課題】しかるに、この方法
は、消化反応の速度が遅く、水の予熱温度をできるだけ
高くしても、5〜16時間という長時間が必要で、しか
もこのように時間をかけても、通常85〜90%程度の
反応率しか得られない。軽焼酸化マグネシウムは、か焼
時の塊状鉱石の大小などでか焼条件が不均一となり、こ
れが原因で消化反応させにくいものが混入してくるため
である。
However, this method has a slow digestion reaction rate and requires a long time of 5 to 16 hours even if the preheating temperature of water is as high as possible. Even if it is applied, a reaction rate of about 85 to 90% is usually obtained. This is because lightly burned magnesium oxide has uneven calcination conditions due to the size of massive ores during calcination, which causes the inclusion of substances that are difficult to undergo a digestion reaction.

【0004】この発明は、上記従来の事情に鑑み、軽焼
酸化マグネシウムの消化方法に改良を加えることによ
り、消化反応性を向上させ、反応時間の短縮と反応率を
高めることを目的としている。
In view of the above-mentioned conventional circumstances, the present invention aims to improve the digestion reactivity by shortening the reaction time and increase the reaction rate by improving the digestion method of light burned magnesium oxide.

【0005】[0005]

【課題を解決するための手段】この発明者らは、上記の
目的を達成するため、鋭意検討した結果、まず、軽焼酸
化マグネシウムの消化反応は粒子表面から起こり、これ
に伴い粒子表面に水酸化マグネシウム層が生成して、こ
の層を介した粒子内部への水の拡散が消化反応の律速と
なつているものと考えた。
Means for Solving the Problems The inventors of the present invention have conducted extensive studies in order to achieve the above-mentioned object. As a result, first, the digestion reaction of light-baked magnesium oxide occurs from the particle surface, and the water on the particle surface is accompanied by this. It was considered that the magnesium oxide layer was generated and the diffusion of water into the inside of the particle through this layer was the rate-determining factor for the digestion reaction.

【0006】そこで、上記の拡散を容易にするために、
生成した水酸化マグネシウム層を粒子同志の衝突,分
散,剥離作用などで摩砕する、いわゆる表面粉砕処理を
施しながら、消化反応を進めてみたところ、消化反応性
が格段に向上することを見い出し、この発明を完成する
に至つた。
Therefore, in order to facilitate the above diffusion,
While advancing the digestion reaction while subjecting the generated magnesium hydroxide layer to so-called surface pulverization, in which the particles are crushed by collision, dispersion, peeling action, etc., it was found that the digestion reactivity was significantly improved. This invention has been completed.

【0007】すなわち、この発明は、軽焼酸化マグネシ
ウムの消化反応により水酸化マグネシウムを製造するに
あたり、軽焼酸化マグネシウムの粒子表面に生成する水
酸化マグネシウム層を摩砕しながら消化反応を進めるこ
とを特徴とする水酸化マグネシウムの製造方法に係るも
のである。
That is, according to the present invention, when magnesium hydroxide is produced by a digestion reaction of light-burned magnesium oxide, the digestion reaction is advanced while milling the magnesium hydroxide layer formed on the surface of the particles of light-burned magnesium oxide. The present invention relates to a characteristic method for producing magnesium hydroxide.

【0008】[0008]

【作用】軽焼酸化マグネシウムの粒子表面に生成する水
酸化マグネシウム層は、核となる軽焼酸化マグネシウム
に比べて非常に脆弱なため、容易に摩砕される。粒子表
面層をこのように粉砕処理しながら消化反応を進める
と、粒子表面が常に活性な状態に維持されるため、消化
反応性が飛躍的に向上する。
The magnesium hydroxide layer formed on the surface of the light-burned magnesium oxide particles is much weaker than the light-burned magnesium oxide serving as the core, and is therefore easily ground. When the digestion reaction proceeds while the particle surface layer is pulverized in this way, the particle surface is always kept in an active state, and the digestive reactivity is dramatically improved.

【0009】[0009]

【実施例】以下、この発明の実施例を図面を参考にして
説明する。図1は、この発明の製造方法に適用される装
置の一構成例を示したものである。
Embodiments of the present invention will be described below with reference to the drawings. FIG. 1 shows a structural example of an apparatus applied to the manufacturing method of the present invention.

【0010】図中、1は給水手段1a、軽焼酸化マグネ
シウムの導入手段1b、攪拌機1c、保温機1dが装備
された消化反応槽、2はベンチユリ管からなる表面粉砕
手段、3は攪拌機3aが装備された水酸化マグネシウム
の水スラリ―の貯槽、P1はポンプ、V1,V2はバル
ブである。
In the figure, 1 is a digestion reaction tank equipped with a water supply means 1a, a light burned magnesium oxide introduction means 1b, a stirrer 1c, and a warmer 1d, 2 is a surface crushing means consisting of a bench lily tube, and 3 is a stirrer 3a. Equipped magnesium hydroxide water slurry storage tank, P1 is a pump, V1 and V2 are valves.

【0011】消化反応槽1には、給水手段1aより約3
0〜60℃程度の温水が供給され、ここに導入手段1b
より軽焼酸化マグネシウムを導入して、撹拌機1cによ
り均一な混合撹拌を行つて、消化反応を行わせる。
In the digestion reaction tank 1, about 3 water from the water supply means 1a.
Hot water of about 0 to 60 ° C. is supplied to the introducing means 1b.
A lighter burned magnesium oxide is introduced, and uniform stirring is performed by the stirrer 1c to carry out the digestion reaction.

【0012】この消化反応液は、バルブV1を開放し、
ポンプP1によつて循環経路L1を介して所定の滞留時
間で循環させると共に、この経路L1中に配設したベン
チユリ管からなる表面粉砕手段2により、軽焼酸化マグ
ネシウムの粒子表面に生成してくる水酸化マグネシウム
層を摩砕する。
[0012] This digestion reaction liquid opens the valve V1,
The light is circulated by the pump P1 through the circulation path L1 for a predetermined residence time, and is generated on the particle surface of the light-burned magnesium oxide by the surface crushing means 2 composed of a bench lily pipe arranged in the path L1. Grind the magnesium hydroxide layer.

【0013】すなわち、ベンチユリ管に導入された消化
反応液は、その絞り部2aで流速が加速され、粒子同志
ないし壁面との強力な衝突による摩耗,剥離作用を受け
ることにより、粒子表面層の水酸化マグネシウム層が簡
単に削り取られる。
That is, the digestion reaction liquid introduced into the bench lily tube is accelerated in its flow velocity at the narrowed portion 2a thereof, and is subjected to the abrasion and peeling action due to the strong collision with the particles or the wall surface. The magnesium oxide layer is easily scraped off.

【0014】このように摩砕しながら消化反応を進める
と、その反応速度は、従来方法(消化反応槽1内で通常
の撹拌を行いながら消化反応させる方法)に比べて著し
く速くなり、加える動力の強さにより通常1/3〜1/
10程度の短時間で反応が完結する。なお、反応が完結
したかどうかは、粘度上昇や反応熱による昇温の様子を
調べることにより、簡単に確認できる。
When the digestion reaction proceeds while milling in this manner, the reaction rate becomes remarkably faster than the conventional method (method in which the digestion reaction is carried out in the digestion reaction tank 1 while performing normal stirring), and the power to be applied is increased. Usually 1/3 to 1 / depending on the strength of
The reaction is completed in a short time of about 10. Whether or not the reaction is completed can be easily confirmed by examining the state of temperature increase due to viscosity increase or reaction heat.

【0015】このような消化反応により、軽焼酸化マグ
ネシウムは、水酸化マグネシウムの水スラリ―となり、
バルブV2の開放で撹拌機3aを有する貯槽3に導か
れ、撹拌状態で貯蔵される。この水スラリ―は、排液の
中和剤や排煙脱硫用のアルカリ剤などとして、種々の産
業分野にそのまま利用される。
By such a digestion reaction, the light-burned magnesium oxide becomes a water slurry of magnesium hydroxide,
When the valve V2 is opened, it is guided to the storage tank 3 having the stirrer 3a and stored in a stirred state. This water slurry is used as it is in various industrial fields as a neutralizing agent for effluent, an alkaline agent for flue gas desulfurization, and the like.

【0016】なお、上記の例では、表面粉砕手段2とし
て、ベンチユリ管を用いているが、これと同じ作用があ
るオリフイスやノズルであつてもよく、急角度で流れ方
向が変わるスタテイツクミキサ―などを用いてもよい。
また、高速回転羽根ないし刃と固定壁との間で衝突,分
散,剥離作用を示す家庭用のジユ―サ―ミキサ―などを
耐摩耗性の材料構成としたものであつてもよい。
In the above example, a bench lily tube is used as the surface crushing means 2, but an orifice or a nozzle having the same function as this may be used, and a static mixer whose flow direction changes at a steep angle. Etc. may be used.
Further, a household-use mixer having a high-speed rotating blade or blade and collision, dispersion, and peeling action between the fixed wall and the like may be made of a wear-resistant material.

【0017】図2は、この発明の製造方法に適用される
装置の他の構成例を示したもので、図1における循環経
路L1を省いて、表面粉砕手段2を消化反応槽1内に直
接設けたものである。この場合、上記粉砕手段2とし
て、図に示す高速撹拌機、たとえば(株)島崎製作所製
のミクロアジタ―が好ましく用いられる。
FIG. 2 shows another structural example of the apparatus applied to the manufacturing method of the present invention. The circulation path L1 in FIG. 1 is omitted, and the surface crushing means 2 is directly placed in the digestion reaction tank 1. It is provided. In this case, as the crushing means 2, a high-speed stirrer shown in the figure, for example, Micro Agitator manufactured by Shimazaki Seisakusho Co., Ltd. is preferably used.

【0018】この高速撹拌機は、モ―タ21で高速回転
するシヤフト22の下部先端側に、図3に示すように撹
拌羽根23が装備されて、かつこれを取り囲む固定壁2
4が固定支持筒25に付設されている。消化反応液は、
上記支持筒25の開口部26と下部先端側より吸い込ま
れ、上記羽根23と固定壁24との間で表面粉砕され
て、隙間27から流出する。
In this high-speed agitator, a stirring blade 23 is provided on the lower tip side of a shaft 22 which rotates at a high speed by a motor 21 as shown in FIG.
4 is attached to the fixed support cylinder 25. The digestion reaction solution is
It is sucked from the opening 26 and the lower end side of the support cylinder 25, surface-crushed between the blade 23 and the fixed wall 24, and flows out from the gap 27.

【0019】なお、言うまでもないが、消化反応槽1内
に装備される攪拌機1cは、原料の軽焼酸化マグネシウ
ムや反応生成物である水酸化マグネシウムが槽下部に沈
降しない程度に撹拌混合するための通常の撹拌機であつ
て、上記高速撹拌機2の如き表面粉砕作用を持たないも
のである。
Needless to say, the stirrer 1c provided in the digestion reaction tank 1 is for stirring and mixing the light burned magnesium oxide as a raw material and magnesium hydroxide as a reaction product so as not to settle at the bottom of the tank. This is a normal stirrer, which does not have a surface crushing action like the high speed stirrer 2 described above.

【0020】このようにして消化反応させたのち、ポン
プP2により、撹拌機3aを有する貯槽3に導き、撹拌
状態で貯蔵する。この装置構成によると、循環経路L1
を省けるため、図1の装置構成のものに比べてよりコン
パクトにでき、消化反応装置の小型化や低コスト化に一
層寄与させることができる。
After the digestion reaction is carried out in this manner, it is led to the storage tank 3 having the stirrer 3a by the pump P2 and stored in a stirring state. According to this device configuration, the circulation path L1
Since it can be omitted, it can be made more compact than that of the apparatus configuration of FIG. 1, and can further contribute to downsizing and cost reduction of the digestion reaction apparatus.

【0021】[0021]

【発明の効果】以上のように、この発明では、軽焼酸化
マグネシウムの粒子表面に生成する水酸化マグネシウム
層を摩砕しながら消化反応を進めるものであるため、消
化反応性が著しく向上し、反応時間を従来に比べて格段
に短縮できると共に、100%の反応率を得ることもで
きる。
As described above, according to the present invention, since the digestion reaction is advanced while milling the magnesium hydroxide layer formed on the surface of the particles of light-burned magnesium oxide, the digestion reactivity is remarkably improved, The reaction time can be remarkably shortened as compared with the conventional one, and a reaction rate of 100% can be obtained.

【0022】このため、消化反応に際し、水の予熱温度
をそれほど高くする必要がなく、そのぶん蒸気の消費コ
ストが減り、また消化反応装置を小型化することが可能
で、さらに消化反応の連続化も容易である。また、用い
る軽焼酸化マグネシウムは、粒子径が比較的粗くても良
好な消化反応を期待できるため、粉砕時の動力の低減や
粉砕設備の小型化にも好結果が得られ、また見掛け比重
の低下で長距離輸送での体積が減少し、運賃が安くなる
などの効果も得られる。
Therefore, in the digestion reaction, it is not necessary to raise the preheating temperature of water so much, the consumption cost of steam is reduced accordingly, and the digestion reaction apparatus can be downsized, and the digestion reaction can be continued. Is also easy. In addition, since the light-burned magnesium oxide used can be expected to have a good digestion reaction even if the particle size is relatively coarse, good results can be obtained in reducing the power during pulverization and downsizing the pulverization equipment, and also in terms of apparent specific gravity. As a result, the volume for long-distance transportation will decrease, and the fare will be cheaper.

【図面の簡単な説明】[Brief description of drawings]

【図1】この発明の製造方法に適用する装置の一構成例
を示す概略図である。
FIG. 1 is a schematic view showing one structural example of an apparatus applied to a manufacturing method of the present invention.

【図2】この発明の製造方法に適用する装置の他の構成
例を示す概略図である。
FIG. 2 is a schematic view showing another configuration example of an apparatus applied to the manufacturing method of the present invention.

【図3】図2のA−A線断面図である。3 is a cross-sectional view taken along the line AA of FIG.

【符号の説明】[Explanation of symbols]

1 消化反応槽 1a 給水手段 1b 軽焼酸化マグネシウムの導入手段 2 表面粉砕手段(ベンチユリ管、高速撹拌機) 3 水酸化マグネシウムの水スラリ―の貯槽 1 digestion reaction tank 1a water supply means 1b light burned magnesium oxide introduction means 2 surface crushing means (bench lily tube, high speed agitator) 3 magnesium hydroxide water slurry storage tank

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 軽焼酸化マグネシウムの消化反応により
水酸化マグネシウムを製造するにあたり、軽焼酸化マグ
ネシウムの粒子表面に生成する水酸化マグネシウム層を
摩砕しながら消化反応を進めることを特徴とする水酸化
マグネシウムの製造方法。
1. When producing magnesium hydroxide by a digestion reaction of light-burned magnesium oxide, water is characterized in that the digestion reaction proceeds while milling a magnesium hydroxide layer formed on the surface of particles of light-burned magnesium oxide. Method for producing magnesium oxide.
JP10178592A 1992-03-28 1992-03-28 Production of magnesium hydroxide Pending JPH05279018A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10178592A JPH05279018A (en) 1992-03-28 1992-03-28 Production of magnesium hydroxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10178592A JPH05279018A (en) 1992-03-28 1992-03-28 Production of magnesium hydroxide

Publications (1)

Publication Number Publication Date
JPH05279018A true JPH05279018A (en) 1993-10-26

Family

ID=14309842

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10178592A Pending JPH05279018A (en) 1992-03-28 1992-03-28 Production of magnesium hydroxide

Country Status (1)

Country Link
JP (1) JPH05279018A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013079161A (en) * 2011-10-03 2013-05-02 Teijin Engineering Ltd Method for producing magnesium oxide composition, magnesium oxide composition, neutralizing agent for desulfurization, method for desulfurizing flue gas, and apparatus for desulfurizing flue gas
WO2015058236A1 (en) 2013-10-24 2015-04-30 Calix Ltd Process and apparatus for manufacture of hydroxide slurry
EP3012222A4 (en) * 2013-06-19 2017-03-08 Dalian Maritime University Preparation method and device for efficiently preparing magnesium hydroxide
US10603293B2 (en) 2010-01-14 2020-03-31 Crescita Therapeutics Inc. Solid-forming local anesthetic formulations for pain control
CN111116061A (en) * 2019-12-31 2020-05-08 米易东立矿业有限公司 Dry preparation method of nano calcium hydroxide

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10603293B2 (en) 2010-01-14 2020-03-31 Crescita Therapeutics Inc. Solid-forming local anesthetic formulations for pain control
US10751305B2 (en) 2010-01-14 2020-08-25 Crescita Therapeutics Inc. Solid-forming topical formulations for pain control
JP2013079161A (en) * 2011-10-03 2013-05-02 Teijin Engineering Ltd Method for producing magnesium oxide composition, magnesium oxide composition, neutralizing agent for desulfurization, method for desulfurizing flue gas, and apparatus for desulfurizing flue gas
EP3012222A4 (en) * 2013-06-19 2017-03-08 Dalian Maritime University Preparation method and device for efficiently preparing magnesium hydroxide
WO2015058236A1 (en) 2013-10-24 2015-04-30 Calix Ltd Process and apparatus for manufacture of hydroxide slurry
US10358364B2 (en) 2013-10-24 2019-07-23 Calix Ltd Process and apparatus for manufacture of hydroxide slurry
US10800683B2 (en) 2013-10-24 2020-10-13 Calix Ltd Process for manufacture of hydroxide slurry
US11401183B2 (en) 2013-10-24 2022-08-02 Calix Ltd Process for manufacture of hydroxide slurry
CN111116061A (en) * 2019-12-31 2020-05-08 米易东立矿业有限公司 Dry preparation method of nano calcium hydroxide

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