JPS58176124A - Preparation of calcium hydroxide plate crystal - Google Patents
Preparation of calcium hydroxide plate crystalInfo
- Publication number
- JPS58176124A JPS58176124A JP6005682A JP6005682A JPS58176124A JP S58176124 A JPS58176124 A JP S58176124A JP 6005682 A JP6005682 A JP 6005682A JP 6005682 A JP6005682 A JP 6005682A JP S58176124 A JPS58176124 A JP S58176124A
- Authority
- JP
- Japan
- Prior art keywords
- calcium
- calcium hydroxide
- acid
- aqueous solution
- plate
- 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】
不発明は、粒度の揃った板状水酸化力ルンウム結晶の製
造方法に関し、さらに詳しくは、弱酸又はそのカルシウ
ム塩を含有する水溶液中において酸化カルシウムを水和
反応させることにより、板状の水酸化カルシウム結晶を
製造する方法に関するものである。[Detailed Description of the Invention] The invention relates to a method for producing plate-like hydroxide crystals with uniform particle size, and more specifically, a method for hydrating calcium oxide in an aqueous solution containing a weak acid or its calcium salt. This invention relates to a method for producing plate-shaped calcium hydroxide crystals.
水酸化カルシウムは消石灰の名称で知られ、わが国にお
いては資源的に恵まれていて安価である1こめ、多(の
用途に、例えば農地改良剤、建築における白壁材、公害
対策としての排煙中の亜硫酸ガス回収剤、海水からマグ
ネシウムの資源採集のためのアルカリ源、あるいは漂白
剤やソーダ用、紙バルブ用などの化学工業用として幅広
く用(・られている。Calcium hydroxide is known by the name of slaked lime, and in Japan it is a rich resource and is inexpensive.It is used for many purposes, such as as a farmland improvement agent, as a white wall material in buildings, and in flue gas as a pollution control measure. It is widely used as a sulfur dioxide gas recovery agent, an alkali source for collecting magnesium resources from seawater, and for chemical industry applications such as bleach, soda, and paper valves.
ところで、これらの用途に水酸化カルシウムを用いる場
合、通常、その用途に応じた粒子の太きさや形状を有す
るものが好まれる。例えば、農業用肥料向けには、反応
が遅鈍型の粒子の太き(・ものが望まれ、亜硫酸ガス回
収剤用には、煙道中の酎薄な亜硫酸ガスとの反応を瞬時
にかつ完全に行わせしめる必要があるため、コロイド状
の極めて細い粒子の水酸化カルシウムが使用される。1
だ左官用には可塑性、安定性、保水性や白さが要求され
、これらの性質を得るためには板状であることが必要で
あるといわれている。By the way, when calcium hydroxide is used for these uses, it is usually preferable to use calcium hydroxide having a particle size and shape depending on the use. For example, for agricultural fertilizers, thick particles with a slow reaction are desired, and for sulfur dioxide gas recovery agents, the reaction with dilute sulfur dioxide in the flue is instantaneous and complete. Therefore, colloidal calcium hydroxide in extremely fine particles is used.1
Plasticity, stability, water retention, and whiteness are required for plastering, and it is said that in order to obtain these properties, it is necessary to have a plate shape.
しかしながら、このように水酸化カルシウムはその形状
や粒子の大きさの制御が必要でちるにもかかわらず、従
来そのための十分な考慮が払われているとはいえない。However, although it is necessary to control the shape and particle size of calcium hydroxide, it cannot be said that sufficient consideration has been given to this in the past.
この水酸化カルシウム(凍、通常石灰岩をか焼して生石
灰(Oak)を得、これを乾式法又は湿式法で水和する
ことによって得られており、その反応過程を示すと次の
とおりである。This calcium hydroxide (Oak) is obtained by calcining limestone and hydrating it using a dry or wet method.The reaction process is as follows. .
か焼
0aCO3−一→C!aO+002−−− (1)Oa
O+H2O−→C!a(OH)2 −−−(11)こ
のようにして製造された水酸化カルシウムの粉末は、第
1図の顕微鏡写真から分るように、粒子は固結状態であ
って、粒度も極めて不揃いである。Calcination 0aCO3-1→C! aO+002--- (1) Oa
O+H2O-→C! a(OH)2 ---(11) As can be seen from the micrograph in Figure 1, the calcium hydroxide powder produced in this way has particles in a consolidated state, and the particle size is extremely irregular. It is.
不発明者らは、このような事情に鑑み、固結状態の水酸
化カルシウムの粒子を単に粉砕分級して粒度な揃えるの
ではなく、個々の水酸化カルシウムの結晶の形状や粒子
の大きさを積極的に制御する方法を開発丁べ(鋭意研究
を重ねた結果、弱酸又はそのカルシウム塩を含有する水
溶液中で酸化カルシウムを水和させて水酸化カルシウム
を得る方法が、その目的を達成しうろことを見出し、こ
の知見に基づいて不発明を完成するに至った。In view of these circumstances, the inventors did not simply crush and classify the particles of calcium hydroxide in the solidified state to make the particle size uniform, but instead developed a method to improve the shape and size of individual calcium hydroxide crystals. Development of a method to actively control scales Based on this knowledge, he was able to complete his invention.
すなわち、本発明は、酸化カルシウムの水和反応により
水酸化カルシウムを製造でるに当り、弱酸又はそのカル
シウム塩を含有する水溶液中におし・で、酸化カルシウ
ムを水和させることを特徴とする板状水酸化カルシウム
結晶の製造方法を提供するものである。That is, the present invention provides a plate characterized in that, in producing calcium hydroxide through a hydration reaction of calcium oxide, calcium oxide is hydrated in an aqueous solution containing a weak acid or its calcium salt. The present invention provides a method for producing calcium hydroxide crystals.
不発明方法において原料として用いる酸化力ルンウムは
、炭酸カルシウムを主成分とする石灰岩や貝殻などを熱
分解することにより、また水酸化カルシウムを脱水する
ことによって得られる。この熱分解や脱水の温度は、6
00〜1400℃の範囲が好ましいが、特に1000℃
前後が好適である。Oxidizing runium used as a raw material in the uninvented method can be obtained by thermally decomposing limestone or shells containing calcium carbonate as a main component, or by dehydrating calcium hydroxide. The temperature of this thermal decomposition and dehydration is 6
The range of 00 to 1400°C is preferable, especially 1000°C
The front and rear are preferred.
また、本発明方法において水和反応に用いる水溶液に含
有させる弱酸又はそのカルシウム塩の酸基については、
弱酸であれば特に制限はないが、好ましくは、酢酸、ア
クリル酸、ギ酸、乳酸、酪酸などの有機酸である。In addition, regarding the acid group of the weak acid or its calcium salt contained in the aqueous solution used for the hydration reaction in the method of the present invention,
There are no particular limitations as long as it is a weak acid, but organic acids such as acetic acid, acrylic acid, formic acid, lactic acid, and butyric acid are preferred.
これらの弱酸やそのカルシウム塩の水溶液における濃度
は、0.1〜lO重f#4の範囲が好ましく、特に0.
5〜5重量重量節囲が好適である。The concentration of these weak acids and their calcium salts in an aqueous solution is preferably in the range of 0.1 to 1O f#4, particularly 0.1 to 1O f#4.
A weight range of 5 to 5 is preferred.
不発明方法における酸化カルシウムの使用量は、前記水
溶液100重量部に対して1〜30重量部が適当である
が、さらに好ましべは10〜20重量部の範囲である。The amount of calcium oxide used in the uninvented method is suitably 1 to 30 parts by weight, more preferably 10 to 20 parts by weight, based on 100 parts by weight of the aqueous solution.
不発明方法において、酸化カルシウムの水和反応によっ
て生成でる水酸化カルシウムの結晶成長速度は速く、反
応開始後τぐにも板状結晶が生成するが、約1日間静置
しておけば、第2図の顕微鏡写真で示されているように
、厚さ0.3μm1板の直径311n 程度の粒度のよ
(揃った板状形を有する結晶粒子が多数生成する。さら
に長時間静置しておくと、この水酸化カルシウムの結晶
はより大きなものとなる。静置している間の温度は0〜
90°Cの範囲が望ましく、特に室温での静置が好適で
ある。このようにして得られた水酸化カルシウムは、そ
の粒子が板状で大きいのでろ過や脱水が容易であり、さ
らに粒子そのものが単結晶体であるため、純度が高くて
不純物を含まない。ま1ころ液はくり返し使用が可能で
あって経済的である。In the uninvented method, the crystal growth rate of calcium hydroxide produced by the hydration reaction of calcium oxide is fast, and plate-like crystals are produced shortly after the reaction starts, but if left standing for about one day, the second crystal will grow. As shown in the micrograph in the figure, a large number of crystal grains with a uniform plate shape are produced, with a particle size of about 311 nm in diameter per plate with a thickness of 0.3 μm. , this calcium hydroxide crystal becomes larger.The temperature while standing is 0~
A temperature in the range of 90°C is desirable, and standing at room temperature is particularly preferred. Calcium hydroxide thus obtained has large, plate-shaped particles, making it easy to filter and dehydrate, and since the particles themselves are single crystals, they are highly pure and do not contain impurities. The roller solution can be used repeatedly and is economical.
不発明方法によって得られる水酸化カルシウムは、左官
用材料として要求されている性質をみたすのみならず、
複合材料のフィラーとしてもその形状特性を利用しうる
。Calcium hydroxide obtained by the uninvented method not only satisfies the properties required as a material for plastering, but also
Its shape characteristics can also be used as a filler for composite materials.
次に実施例によって不発明をさらに詳細に説明する0
実施例1
1電蓄16酢酸カルシウム水溶液Zoo cc中に、炭
酸カルシウムを1000℃で1時間加熱処理して得られ
た酸化カルシウム(生石灰)10.9を入れ、よ(かき
まぜたのち、密栓をして室温で1日間静置した。これを
ろ過、乾燥して得た水酸化カルシウム粉末を走査型電子
顕微鏡で観察したところ、板状結晶で、厚さ0.3μm
1板の直径2.5〜3μmの粒度の揃った結晶であった
。Next, the non-invention will be explained in more detail with reference to examples.0 Example 1 1 Electric storage 16 Calcium oxide (quicklime) obtained by heating calcium carbonate at 1000°C for 1 hour in a calcium acetate aqueous solution Zoo cc 10 After stirring, it was sealed tightly and allowed to stand at room temperature for one day. When the calcium hydroxide powder obtained by filtering and drying was observed with a scanning electron microscope, it was found to be plate-shaped crystals. , thickness 0.3μm
The crystals had a uniform particle size with a diameter of 2.5 to 3 μm per plate.
実施例2
酢酸カルシウムの5重量係水溶液100cc中に、水酸
化カルシウムを1000℃で脱水して得た酸化カルシウ
ム(生石灰)10Iを入れ、かきまぜたのち、90℃で
1日間静置して得た水酸化カルシウム粉末は、厚さ0.
1μm1板の直径約1.5μmの薄板状の結晶であった
。Example 2 10 I of calcium oxide (quicklime) obtained by dehydrating calcium hydroxide at 1000° C. was added to 100 cc of a 5 weight aqueous solution of calcium acetate, stirred, and then allowed to stand at 90° C. for 1 day. Calcium hydroxide powder has a thickness of 0.
It was a thin plate-like crystal with a diameter of about 1.5 μm and one plate of 1 μm.
実施例3
0.5重量幅の酢酸水溶液100cc中に、1400℃
でか焼して得た酸化カルシウム17.9をかきまぜなが
ら投入したのち、0℃で1日間静置後、ろ過、乾燥して
得た水酸化カルシウム粉末は、板の厚さ0.3μm1板
の直径3〜3.5μmの粒度の揃った結晶であった。Example 3 1400°C in 100cc of acetic acid aqueous solution of 0.5 weight range
The calcium hydroxide powder obtained by stirring and adding calcium oxide 17.9% obtained by calcining, allowing it to stand at 0°C for 1 day, filtering and drying the powder, has a thickness of 0.3 μm per plate. The crystals had a uniform particle size of 3 to 3.5 μm in diameter.
実施例4
2重量幅のアクリル酸カルシウム水溶液100cc中に
水酸化カルシウムを1000℃で処理して得た酸化カル
シウム10gを入れ、かきまぜたのち、室温で1日間静
置した。ろ過、乾燥して得られた水酸化カルシウム粉末
は、厚さ0.3μm1板の直径約2.5μmの板状結晶
であった。Example 4 10 g of calcium oxide obtained by treating calcium hydroxide at 1000° C. was added to 100 cc of a 2-weight width calcium acrylate aqueous solution, stirred, and then allowed to stand at room temperature for 1 day. The calcium hydroxide powder obtained by filtration and drying was plate-shaped crystals with a diameter of about 2.5 μm and one plate with a thickness of 0.3 μm.
実施例5
1重量幅のギ酸カルシウム水溶液100cc中に、酸化
カルシウム10Iを入れ、かきまぜたのち、室温で2日
間静置して得た水酸化カルシウムは、板状で厚さ0.3
μm1板の直径2μmの比較的粒度ノ揃った粉末であっ
た。Example 5 Calcium hydroxide obtained by putting 10 I of calcium oxide into 100 cc of calcium formate aqueous solution of 1 weight range, stirring, and leaving it at room temperature for 2 days was plate-shaped with a thickness of 0.3
The powder was relatively uniform in particle size with a diameter of 2 μm per μm plate.
第1図は、走査型電子顕微鏡で観察した市販の水酸カル
シウムの写真であり、第2図は、不発明方法による1重
量幅酢酸カルシウム水溶液を用いて酸化カルシウムを水
和して得た板状水酸化カルシウムの写真である。なお倍
率は10000倍である。
特許出願人 工業技術院長 石 坂 誠 −指定代理
人 工業技術院大阪工業技術試験所長内藤−男Figure 1 is a photograph of commercially available calcium hydroxide observed with a scanning electron microscope, and Figure 2 is a plate obtained by hydrating calcium oxide using a 1-weight width calcium acetate aqueous solution by an uninvented method. This is a photograph of calcium hydroxide. Note that the magnification is 10,000 times. Patent applicant: Makoto Ishizaka, Director of the Agency of Industrial Science and Technology - Designated agent: Naito, Director of the Osaka Institute of Industrial Science and Technology, Agency of Industrial Science and Technology
Claims (1)
を製造するに当り、弱酸又はそのカルシウム塩を含有す
る水溶液中において、酸化カルシウムを水和させろこと
を特徴とてる板状水酸化カルシウム結晶の製造方法。1. Production of plate-shaped calcium hydroxide crystals characterized in that calcium oxide is hydrated in an aqueous solution containing a weak acid or its calcium salt when producing calcium hydroxide by a hydration reaction of calcium oxide. Method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6005682A JPS58176124A (en) | 1982-04-10 | 1982-04-10 | Preparation of calcium hydroxide plate crystal |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6005682A JPS58176124A (en) | 1982-04-10 | 1982-04-10 | Preparation of calcium hydroxide plate crystal |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58176124A true JPS58176124A (en) | 1983-10-15 |
JPS6324939B2 JPS6324939B2 (en) | 1988-05-23 |
Family
ID=13131040
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6005682A Granted JPS58176124A (en) | 1982-04-10 | 1982-04-10 | Preparation of calcium hydroxide plate crystal |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58176124A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010111532A (en) * | 2008-11-05 | 2010-05-20 | Okutama Kogyo Co Ltd | Method for producing planar calcium hydroxide |
BE1018979A4 (en) * | 2008-10-30 | 2011-12-06 | Lhoist Rech Et Dev | DETACHED LIME COMPOSITIONS AND METHOD FOR MANUFACTURING SAME. |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57106521A (en) * | 1980-12-24 | 1982-07-02 | Yahashi Kogyo Kk | Manufacture of light granular slaked lime |
-
1982
- 1982-04-10 JP JP6005682A patent/JPS58176124A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57106521A (en) * | 1980-12-24 | 1982-07-02 | Yahashi Kogyo Kk | Manufacture of light granular slaked lime |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE1018979A4 (en) * | 2008-10-30 | 2011-12-06 | Lhoist Rech Et Dev | DETACHED LIME COMPOSITIONS AND METHOD FOR MANUFACTURING SAME. |
JP2010111532A (en) * | 2008-11-05 | 2010-05-20 | Okutama Kogyo Co Ltd | Method for producing planar calcium hydroxide |
Also Published As
Publication number | Publication date |
---|---|
JPS6324939B2 (en) | 1988-05-23 |
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