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JPS5834410B2 - Shinjiyou Alpha Agata Hansu Isetsu Kono Seizouhou - Google Patents
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JPS5834410B2 - Shinjiyou Alpha Agata Hansu Isetsu Kono Seizouhou - Google Patents

Shinjiyou Alpha Agata Hansu Isetsu Kono Seizouhou

Info

Publication number
JPS5834410B2
JPS5834410B2 JP13696875A JP13696875A JPS5834410B2 JP S5834410 B2 JPS5834410 B2 JP S5834410B2 JP 13696875 A JP13696875 A JP 13696875A JP 13696875 A JP13696875 A JP 13696875A JP S5834410 B2 JPS5834410 B2 JP S5834410B2
Authority
JP
Japan
Prior art keywords
gypsum
slurry
shinjiyou
seizouhou
isetsu
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
Application number
JP13696875A
Other languages
Japanese (ja)
Other versions
JPS5261197A (en
Inventor
芳雄 金正
幸雄 滝川
敏則 堤
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Chemical Industries Ltd
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 Mitsubishi Chemical Industries Ltd filed Critical Mitsubishi Chemical Industries Ltd
Priority to JP13696875A priority Critical patent/JPS5834410B2/en
Publication of JPS5261197A publication Critical patent/JPS5261197A/en
Publication of JPS5834410B2 publication Critical patent/JPS5834410B2/en
Expired 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
    • C01F11/00Compounds of calcium, strontium, or barium
    • C01F11/46Sulfates
    • C01F11/466Conversion of one form of calcium sulfate to another

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)

Description

【発明の詳細な説明】 本発明は針状α型手水石膏の製造方法に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing acicular α-type hand washing plaster.

石膏には種々の結晶構造があるが、α型半水石膏は強度
の点で優れており、就中、針状α型半水石膏は特殊な用
途、例えば、合成樹脂用充填部り紙力増強剤等の分野で
の利用に適してることが知られている。
Gypsum has various crystal structures, but α-type hemihydrate gypsum is superior in terms of strength. In particular, acicular α-type hemihydrate gypsum is used for special purposes, such as paper strength in filling parts for synthetic resins. It is known that it is suitable for use in fields such as enhancers.

この針状α型半水石膏の製造方法としては、三水石膏と
水とのスラリーを適当な媒晶剤の存在下に加圧下、加熱
処理する方法が知られている。
As a method for producing this acicular α-type hemihydrate gypsum, a method is known in which a slurry of trihydrate gypsum and water is heat-treated under pressure in the presence of a suitable crystallizing agent.

しかしながら、従来公知の方法では、反応に長時間を要
すると共に、反応中にスラリーがゲル状となり易く、そ
のため、工業的実施に当っては攪拌、分離操作等に種々
のトラブルを与えると言う欠点がある。
However, in the conventionally known methods, the reaction takes a long time and the slurry tends to become gel-like during the reaction, which has the disadvantage of causing various troubles in stirring, separation operations, etc. in industrial implementation. be.

本発明者等は上記実情に鑑み、針状α型半水石膏の工業
的有利な製造方法につき種々検討した結果、成る特定の
媒晶剤を組合わせて使用する場合は、短時間にして、し
かも、スラリーがゲル化を呈することなく針状α型半水
石膏を得ることができるという知見を得、本発明を完成
した。
In view of the above circumstances, the present inventors have conducted various studies on industrially advantageous production methods for acicular α-type hemihydrate gypsum, and have found that when using a combination of specific crystal modifiers, Furthermore, the present invention was completed based on the knowledge that acicular α-type hemihydrate gypsum can be obtained without the slurry exhibiting gelation.

すなわち、本発明の要旨は、三水石膏と水よりなるスラ
リーを加圧下、加熱処理してα型半水石膏を製造するに
際し、 (1)クエン酸、酒石酸又はフマル酸のナトリウム塩か
ら選ばれた少なくとも一種の化合物と(2)アルミニウ
ム、鉄又はニッケルの硫酸塩から選ばれた少なくとも一
種の化合物 (但し、クエン酸ナトリウムと硫酸ニッケルとの組合わ
せを除く)とを媒晶剤として、該スラリー中に存在させ
ることを特徴とする針状α型半水石膏の製造方法に存す
る。
That is, the gist of the present invention is that when producing α-type hemihydrate by heat-treating a slurry consisting of gypsum trihydrate and water under pressure, (1) a sodium salt of citric acid, tartaric acid, or fumaric acid is and (2) at least one compound selected from sulfates of aluminum, iron, or nickel (excluding the combination of sodium citrate and nickel sulfate) as a modifier. The invention relates to a method for producing acicular α-type hemihydrate gypsum.

本発明の詳細な説明するに、本発明で適用される三水石
膏としては、例えば、天然石膏、排煙脱硫石膏等が挙げ
られる。
To explain the present invention in detail, examples of the trihydrate gypsum applied in the present invention include natural gypsum, flue gas desulfurization gypsum, and the like.

これらの石膏は、通常、50μ〜80μ程度に均一に粉
砕したのち、水と混合して石膏スラリーとされる。
These gypsums are usually ground to a uniform size of about 50 to 80 microns, and then mixed with water to form a gypsum slurry.

この際の水の量は、通常、石膏に対して2〜100重量
倍、好ましくは、3〜100重量倍の範囲から選ばれる
The amount of water at this time is usually selected from a range of 2 to 100 times the weight of gypsum, preferably 3 to 100 times the weight of gypsum.

このように調整されたスラリーは、通常、オートクレー
ブ等の耐圧容器を使用して攪拌下、1〜8Kf/crt
l Gの加圧下に加熱処理される。
The slurry prepared in this way is usually stirred in a pressure-resistant container such as an autoclave at a rate of 1 to 8 Kf/crt.
Heat treated under pressure of 1 G.

加熱処理温度は、通常、110〜150℃、好ましくは
、120〜130℃であり、処理時間は1〜3時間、好
ましくは、1〜2時間程度である。
The heat treatment temperature is usually 110 to 150°C, preferably 120 to 130°C, and the treatment time is about 1 to 3 hours, preferably about 1 to 2 hours.

本発明では、上述の加熱処理を特定の組合わせの媒晶剤
の存在下に行なうことにより、針状α型半水石膏を得る
のである。
In the present invention, acicular α-type hemihydrate gypsum is obtained by performing the above-mentioned heat treatment in the presence of a specific combination of crystal modifiers.

本発明は媒晶剤としてクエン酸、酒石酸又はフマル酸の
ナトリウム塩と、アルミニウム、鉄又はニッケルの硫酸
塩(但し、クエン酸ナトリウムと硫酸ニッケルとの組合
わせを除く)とを併用使用するものである。
The present invention uses a sodium salt of citric acid, tartaric acid, or fumaric acid together with a sulfate of aluminum, iron, or nickel (excluding the combination of sodium citrate and nickel sulfate) as a crystallizing agent. be.

しかして、これらの媒晶剤の組合わせの好ましい態様と
しては、クエン酸ナトリウムと硫酸アルミニウム、クエ
ン酸ナトリウムと硫酸鉄(特に硫酸第1鉄)、酒石酸ナ
トリウムと硫酸ニッケルが挙げられる。
Preferred combinations of these modifiers include sodium citrate and aluminum sulfate, sodium citrate and iron sulfate (particularly ferrous sulfate), and sodium tartrate and nickel sulfate.

クエン酸ナトリウムと硫酸ニッケルの組合わせの場合は
結晶が柱状となり、目的とする針状α型半水石膏が得ら
れない。
In the case of a combination of sodium citrate and nickel sulfate, the crystals become columnar, and the desired acicular α-type hemihydrate gypsum cannot be obtained.

これらの媒晶剤の石膏に対する添加量は、それぞれ0.
1〜5.0重量宏好ましくは、0.5〜2.0重量袈で
あり、併用割合はほぼ同程度とするのが好ましい。
The amount of each of these crystal modifiers added to the gypsum was 0.
It is 1 to 5.0 weight thick, preferably 0.5 to 2.0 weight thick, and it is preferable that the combined proportions are approximately the same.

これらの媒晶剤は、予め三水石膏中区添※加しても、ス
ラリーの調整後に添加してもよい。
These modifiers may be added to the gypsum trihydrate in advance, or may be added after the slurry is prepared.

加熱処理により生成した針状α型半水石膏は、常法に従
って、沢過、洗浄される。
The acicular α-type hemihydrate gypsum produced by the heat treatment is filtered and washed in a conventional manner.

洗浄後は、通常、90〜150℃の温度で1〜3時間乾
燥され、必要に応じて研磨処理等を施し製品化される。
After washing, it is usually dried at a temperature of 90 to 150° C. for 1 to 3 hours, and if necessary, subjected to polishing treatment or the like to be manufactured into a product.

本発明によれば、特定の媒晶剤を組合わせて使用するこ
とにより、短時間にして、しかも、石膏スラリーのゲル
化現象を呈することなく、針状α型半水石膏を得ること
ができるので、その工業的価値は犬である。
According to the present invention, by using a specific crystal modifier in combination, it is possible to obtain acicular α-type hemihydrate gypsum in a short time and without exhibiting the gelation phenomenon of gypsum slurry. So its industrial value is a dog.

以下、本発明を実施例により更に詳細に説明する。Hereinafter, the present invention will be explained in more detail with reference to Examples.

実施例 三水石膏粉末25S’と水225tjIからなるスラリ
ーに第1表に示した媒晶剤を加え、500−ガラスオー
トクレーブ中で500 rpmで攪拌を行ないながら、
130℃、2.6 Kg/crAGの条件下2時間反応
を行なった。
Example The modifier shown in Table 1 was added to a slurry consisting of 25S' of trihydrate gypsum powder and 225TJI of water, and the mixture was stirred at 500 rpm in a 500-glass autoclave.
The reaction was carried out for 2 hours at 130° C. and 2.6 Kg/crAG.

反応終了後、97’Cで熱r過し、95℃で1時間熱風
乾燥を行なった。
After the reaction was completed, the mixture was heated at 97'C and dried with hot air at 95C for 1 hour.

このようにして得た石膏結晶の結晶構造を示差熱分析し
、また、その結晶形状を光学顕微鏡で観察したところ第
1表に示す結果を得た。
The crystal structure of the gypsum crystal thus obtained was subjected to differential thermal analysis, and the crystal shape was observed using an optical microscope, and the results shown in Table 1 were obtained.

また、製造中、石膏スラリーがゲル状化するということ
はなく、攪拌は始終良好に行なわれ、その後のf過操作
も順調に実施できた。
Further, during production, the gypsum slurry did not gel, stirring was performed well throughout, and the subsequent f-filtering operation was carried out smoothly.

比較例 実施例に於いて、媒晶剤としてクエン酸ナトリウム又は
硫酸ニッケルをそれぞれ単独で使用する他は実施例と同
様にして行なったところ、クエン酸ナトリウム単独使用
の場合は、得られたα型半水石膏は板状であり、また、
硫酸ニッケル単独使用の場合は、得られたα型半水石膏
は針状であつたが、反応の際中、石膏スラリーがゲル化
し、攪拌操作、分離操作が良好に行なわれなかった。
Comparative Example In the example, the same procedure as in the example was carried out except that sodium citrate or nickel sulfate was used alone as a modifier. Gypsum hemihydrate is plate-shaped, and
When nickel sulfate was used alone, the α-type hemihydrate gypsum obtained was acicular, but the gypsum slurry gelled during the reaction, making stirring and separation operations difficult.

Claims (1)

【特許請求の範囲】 1 三水石膏と水よりなるスラリーを加圧下、110〜
150℃で加熱処理してα型半水石膏を製造するに際し
、 (1) クエン酸、酒石酸又はフマル酸のナトリウム
塩から選ばれた少なくとも一種の化合物と(2)アルミ
ニウム、鉄又はニッケルの硫酸塩から選ばれた少なくと
も一種の化合物 (但し、クエン酸す) IJウムと硫酸ニッケルとの組
合わせを除く)とを媒晶剤として、該スラリー中に存在
させることを特徴とする針状α型半水石膏の製造方法。
[Claims] 1. A slurry made of gypsum trihydrate and water is heated under pressure at 110~
When producing α-type hemihydrate gypsum by heat treatment at 150°C, (1) at least one compound selected from sodium salts of citric acid, tartaric acid, or fumaric acid and (2) sulfate of aluminum, iron, or nickel. The acicular α-type semi-semi-acid material is characterized in that at least one compound selected from the following is present in the slurry as a crystal modifier (excluding the combination of citric acid and nickel sulfate). Method of manufacturing hydrogypsum.
JP13696875A 1975-11-14 1975-11-14 Shinjiyou Alpha Agata Hansu Isetsu Kono Seizouhou Expired JPS5834410B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13696875A JPS5834410B2 (en) 1975-11-14 1975-11-14 Shinjiyou Alpha Agata Hansu Isetsu Kono Seizouhou

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13696875A JPS5834410B2 (en) 1975-11-14 1975-11-14 Shinjiyou Alpha Agata Hansu Isetsu Kono Seizouhou

Publications (2)

Publication Number Publication Date
JPS5261197A JPS5261197A (en) 1977-05-20
JPS5834410B2 true JPS5834410B2 (en) 1983-07-26

Family

ID=15187679

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13696875A Expired JPS5834410B2 (en) 1975-11-14 1975-11-14 Shinjiyou Alpha Agata Hansu Isetsu Kono Seizouhou

Country Status (1)

Country Link
JP (1) JPS5834410B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61146718A (en) * 1984-12-15 1986-07-04 Nippon Zeon Co Ltd Aqueous solution of iron compound
JP5535744B2 (en) * 2010-04-22 2014-07-02 株式会社トクヤマ Method for producing resin composition

Also Published As

Publication number Publication date
JPS5261197A (en) 1977-05-20

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