JPS6012337B2 - Metal soap manufacturing method - Google Patents

Metal soap manufacturing method

Info

Publication number
JPS6012337B2
JPS6012337B2 JP5511076A JP5511076A JPS6012337B2 JP S6012337 B2 JPS6012337 B2 JP S6012337B2 JP 5511076 A JP5511076 A JP 5511076A JP 5511076 A JP5511076 A JP 5511076A JP S6012337 B2 JPS6012337 B2 JP S6012337B2
Authority
JP
Japan
Prior art keywords
oxide
hydroxide
parts
water
fatty acid
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
JP5511076A
Other languages
Japanese (ja)
Other versions
JPS52138506A (en
Inventor
克己 岩永
建夫 小林
良一 岡戸
茂 勝又
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.)
Adeka Corp
Original Assignee
Asahi Denka Kogyo KK
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 Asahi Denka Kogyo KK filed Critical Asahi Denka Kogyo KK
Priority to JP5511076A priority Critical patent/JPS6012337B2/en
Publication of JPS52138506A publication Critical patent/JPS52138506A/en
Publication of JPS6012337B2 publication Critical patent/JPS6012337B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は金属石けんの製造方法に関する。[Detailed description of the invention] The present invention relates to a method for manufacturing metal soap.

詳しくは本発明は、溶融法による金属石けんの改良製造
方法に関する。
More specifically, the present invention relates to an improved method for manufacturing metal soap by a melting process.

金属石けんの製造法としては一般に複分解法と溶融法が
知られている。
The double decomposition method and the melting method are generally known as methods for producing metal soap.

複分解法とは、まず、ふつうのアルカリ石けんを製造し
てからこれに金属塩の溶液を加え、複分解によって金属
石けんに変換する方法である。
The double decomposition method is a method in which ordinary alkaline soap is first produced, then a metal salt solution is added to it, and the soap is converted into metal soap through double decomposition.

この方法の欠点は、装置が大規模となるわりには生産量
は低く、大量の用水が必要であり、廃水処理の問題を考
慮しなければならないことである。また、溶融法とは、
脂肪酸を、金属酸化物又は金属水酸化物と共に、高温で
加熱処理し、直接反応させる方法である。これによれば
、反応途上の系は著しく増粘し、縄枠が困難となり、生
成物は塊状であり、粉砕に苦慮することになる。反応温
度が高温のために製品の着色もあって品質も低下する。
また、この時熱0Kを添加すると著しく発泡して反応制
御がむずかしい。本発明の目的は、上記欠点の解消され
た金属石けんの製造方法を提供することにある。
The disadvantages of this method are that the production is low despite the large scale of the equipment, that large amounts of water are required, and that wastewater treatment issues must be considered. Also, what is the melting method?
This is a method in which a fatty acid is heat-treated with a metal oxide or metal hydroxide at a high temperature to cause a direct reaction. According to this, the viscosity of the system in the middle of the reaction increases significantly, making it difficult to form a rope frame, and the product is lumpy, making it difficult to crush. Due to the high reaction temperature, the product becomes discolored and its quality deteriorates.
Furthermore, if 0K heat is added at this time, foaming will occur significantly, making reaction control difficult. An object of the present invention is to provide a method for manufacturing metal soap that eliminates the above-mentioned drawbacks.

すなわち、反応系の増粘と発泡を防ぎ、着色のみられな
い良質の製品を得ることのできる金属石けんの製造方法
を提供することにある。本発明の金属石けんの製造法は
、炭素数6なし、し22を有する高級脂肪酸を融点より
5〜20℃高い温度で溶融させ、これに金属元素の酸化
物および/又は金属元素の水酸化物を均一に分散させた
後、水温5〜55℃の水を高級脂肪酸に対し2.5〜4
0モルの割合で添加し、反応せしめることを特徴とする
。本発明の金属石けんの製造法において、用いられる炭
素数6ないし22を有する高級脂肪酸とは、例えばカプ
リン酸、ラウリン酸、ミリスチン酸、パルミチン酸、ス
テアリン酸もべへン酸等の飽和脂肪酸、オレイン酸「ェ
ルカ酸、リノール酸、リノレイン酸等の不飽和脂肪酸「
あるいはこれらの2種以上の酸の混合酸等があげられる
が、工業的にはステアリン酸が最も適当である。
That is, the object of the present invention is to provide a method for producing metal soap that can prevent thickening and foaming of the reaction system and produce a high-quality product that is free from coloration. The method for producing metallic soap of the present invention involves melting a higher fatty acid having 6 to 22 carbon atoms at a temperature 5 to 20°C higher than its melting point, and adding oxides of metal elements and/or hydroxides of metal elements to this. After uniformly dispersing the higher fatty acids, add water at a temperature of 5 to 55°C to
It is characterized in that it is added at a ratio of 0 mol and allowed to react. In the method for producing metallic soap of the present invention, the higher fatty acids having 6 to 22 carbon atoms used include, for example, saturated fatty acids such as capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, etc. Acids: Unsaturated fatty acids such as erucic acid, linoleic acid, linoleic acid, etc.
Alternatively, mixed acids of two or more of these acids may be used, but stearic acid is industrially most suitable.

また、本発明に用いられる金属元素の酸化物、水酸化物
としては、酸化亜鉛、酸化カドミウム、酸化錫、酸化鉛
、酸化鉄、酸化マグネシウム、酸化カルシウム、酸化バ
リウム、水酸化亜鉛「水酸化カドミウム〜水酸化カルシ
ウム、水酸化錫、水酸化バリウム「水酸化マグネシウム
、水酸化鉛をあげることができ「 また目的物として、
種類の異なる金属を二種以上含む金属石けんを得ようと
するときには、必要とする金属酸化物又は金属水酸化物
を混合して使用することもできる。
In addition, the oxides and hydroxides of metal elements used in the present invention include zinc oxide, cadmium oxide, tin oxide, lead oxide, iron oxide, magnesium oxide, calcium oxide, barium oxide, zinc hydroxide, cadmium hydroxide, ~ Calcium hydroxide, tin hydroxide, barium hydroxide ``Magnesium hydroxide, lead hydroxide can be mentioned'' Also, as objects,
When attempting to obtain a metal soap containing two or more different types of metals, the required metal oxides or metal hydroxides may be mixed and used.

上記の脂肪酸は、これを融点より5〜2ぴ○高い温度に
溶融させ擬梓しながらこの中の金属酸化物、水酸化物を
添加して均一に分散させる。
The above-mentioned fatty acids are melted at a temperature 5 to 2 points higher than the melting point, and the metal oxides and hydroxides are added thereto while the mixture is being melted and uniformly dispersed.

次いで、脂肪酸に対して2.5〜40モル好ましくは5
〜20モルの量の水を加えて反応を行なわせ金属石けん
を得る。この時加える水の水温が高いと添加と同時に急
激な発泡が起り、バルク状に固化した石けんが生成して
、反応のコントロールが困難となる。これに対して、本
発明においては、5〜55℃、好ましくは、10〜30
qo、の水温を有する水を脂肪酸に対して大量に添加す
ることを特徴とする。本発明においては発泡はいちじる
しく少なく「生成する金属石けんは微粒状あるいは、小
さな力で極めて容易に粉砕されうる、もろい粒状を程し
、かつ、白色の良好な色調を有するものである。
Then, 2.5 to 40 mol based on fatty acid, preferably 5
The reaction is carried out by adding water in an amount of ~20 moles to obtain a metal soap. If the temperature of the water added at this time is high, rapid foaming will occur upon addition, producing a bulk solidified soap, making it difficult to control the reaction. On the other hand, in the present invention, the temperature is 5 to 55°C, preferably 10 to 30°C.
It is characterized in that a large amount of water having a water temperature of qo is added to the fatty acid. In the present invention, foaming is significantly reduced, and the metal soap produced is in the form of fine particles or brittle particles that can be crushed very easily with small force, and has a good white color.

このように、顕著な発泡抑制効果を持つため、本発明の
方法によれば、連続的な原料供給が可能になり、反応、
乾燥、粉砕が一連の連続的な工程でできるようになる。
As described above, since the method of the present invention has a remarkable foaming suppressing effect, continuous supply of raw materials is possible, and reaction and
Drying and grinding can be done in a series of continuous steps.

したがって、生産性の高い、また、粉じん公害解消に適
した、経済的な方法といえるのである。なお、反応完了
時に残存する水は、留去、乾燥によって除くことができ
る。本発明の効果は、反応系の増粘と発泡を防ぎ着色の
みられない、良質の金属石けんの製造法を提供したこと
にある。以下「実施例により、さらに詳しく説明するが
、これらは、本発明の範囲を制限するものではない。
Therefore, it can be said to be a highly productive and economical method suitable for eliminating dust pollution. Note that water remaining at the completion of the reaction can be removed by distillation and drying. The effect of the present invention is to provide a method for producing high-quality metal soap that prevents thickening and foaming of the reaction system and does not cause coloring. The following will be described in more detail with reference to Examples, but these are not intended to limit the scope of the present invention.

例中部は全て重量部である。実施例 1 ステアリン酸(SV202、NV201、以下同じ)2
0碇都を反応器に仕込み、加熱「溶融して80℃に調整
する。
All parts in the middle part of the example are by weight. Example 1 Stearic acid (SV202, NV201, same below) 2
Charge 0 Ikarito into a reactor and heat to melt and adjust to 80°C.

これに、酸化カルシウム22部を添加し均一に分散させ
た後、30℃の水200部を徐々に添加する。この時わ
ずかに発泡がみられる。添加後10分間75〜8ぴ0に
加熱燈梓を続けて、反応を終了する。生成した金属石け
んを乾燥し白色細粒状の製品を得る。製品の遊離脂肪較
量は1%である。実施例 2ステアリン酸20の部を反
応器に仕込み、加熱、溶融して80℃に調整する。
After adding 22 parts of calcium oxide and uniformly dispersing it, 200 parts of water at 30°C is gradually added. At this time, slight foaming is observed. After the addition, heating was continued at 75-80°C for 10 minutes to complete the reaction. The produced metallic soap is dried to obtain a white fine granular product. The free fat content of the product is 1%. Example 2 20 parts of stearic acid are charged into a reactor and heated to melt and adjust to 80°C.

これに、酸化マグネシウム18.5部を添加し均一に分
散させた後25午○の水10碇都を徐々に添加する。こ
の時わずかに発泡がみられる。添加後10分間75〜8
0qoに加熱燈拝を続けて、反応を終了する。生成した
金属石けんを乾燥し白色細粒状の製品を得る。製品の遊
離脂肪酸量は0.5%である。実施例 3
‐ ステアリン酸20碇部を反応器に仕込み、加熱、溶融し
て75qoに調整する。
After adding 18.5 parts of magnesium oxide and uniformly dispersing it, 10 parts of 25 ml of water were gradually added. At this time, slight foaming is observed. 75-8 for 10 minutes after addition
Continue heating the lamp to 0qo to complete the reaction. The produced metallic soap is dried to obtain a white fine granular product. The free fatty acid content of the product is 0.5%. Example 3
- Charge 20 parts of stearic acid into a reactor, heat and melt to adjust to 75 qo.

これに水酸化カルシウム27部を添加し均一に分散させ
た後、30℃の水50部を徐々に添加する。この時わず
かに発泡がみられる。添加後10分間75〜80q0に
加熱燈拝を続けて、反応を終了する。生成した金属石け
んを乾燥し白色細粒状の製品を得る。製品の遊離脂肪酸
量は1.3%である。実施例 4 ステアリン酸20碇都を反応器に仕込み、加熱、溶融し
て80午0に調整する。
After adding 27 parts of calcium hydroxide and uniformly dispersing it, 50 parts of water at 30°C is gradually added. At this time, slight foaming is observed. After the addition, heating was continued at 75-80 qO for 10 minutes to complete the reaction. The produced metallic soap is dried to obtain a white fine granular product. The free fatty acid content of the product is 1.3%. Example 4 20 tons of stearic acid was charged into a reactor, heated and melted to adjust the temperature to 80:00.

これに、酸化亜鉛18.5部を添加し均一分散させた後
、50℃の水13碇郭を徐々に添加する。この時わずか
に発泡がみられる。添加後10分間75〜80℃に加熱
嬢梓を続けて、反応を終了する。生成した金属石けんを
乾燥し白色細粒状の製品を得る。製品の遊離脂肪酸量は
1.4%である。実施例 5 ステァリン酸20礎邦を反応器に仕込み、加熱、溶融し
て70qoに調整する。
After adding 18.5 parts of zinc oxide and uniformly dispersing it, 13 parts of water at 50°C are gradually added. At this time, slight foaming is observed. After the addition, continue heating to 75-80°C for 10 minutes to complete the reaction. The produced metallic soap is dried to obtain a white fine granular product. The free fatty acid content of the product is 1.4%. Example 5 20% stearic acid was charged into a reactor and heated and melted to adjust to 70 qo.

これに、水酸化バリウム7$部を添加し均一に分散させ
た後、50qoの水10戊邦を徐々に添加する。この時
わずかに発泡がみられる。添加後1雌ふ間75〜80℃
に加熱燈拝を続けて、反応を終了する。生成した金属石
けんを乾燥し白色細粒状の製品を得る。製品の遊離脂肪
酸量は1.3%である。実施例 6 ステアリン酸20碇部を反応器に仕込み、加熱、溶融し
て7すのこ調整する。
After adding 7 parts of barium hydroxide and uniformly dispersing it, 10 parts of 50 qo of water were gradually added. At this time, slight foaming is observed. 75-80℃ for 1 female after addition
Continue heating the lamp to complete the reaction. The produced metallic soap is dried to obtain a white fine granular product. The free fatty acid content of the product is 1.3%. Example 6 20 parts of stearic acid was charged into a reactor, heated and melted to prepare 7 grates.

これに、酸化カルシウム24部を添加し均一に分散させ
た後、1oo○の水77部を徐々に添加するご この時
わずかに発泡がみられる。添加後10分間75〜8び0
に加熱燈拝を続けて、反応を終了する。生成した金属石
けんを乾燥し白色細粒状の製品を得る。製品の遊離脂肪
酸量は0.8%である。実施例 7 ステアリン酸20碇部を反応器に仕込み、加熱、溶融し
て80こ0に調整する。
After adding 24 parts of calcium oxide and uniformly dispersing it, 77 parts of 1OO○ water was gradually added, and slight foaming was observed. 75-80 for 10 minutes after addition
Continue heating the lamp to complete the reaction. The produced metallic soap is dried to obtain a white fine granular product. The free fatty acid content of the product is 0.8%. Example 7 20 parts of stearic acid was charged into a reactor and heated to melt and adjust to 80 parts.

これに、酸化マグネシウム35部を添加し均一に分散さ
せた後、500の水35部を徐々に添加する。この時わ
ずかに発泡がみられる。添加後10分間75〜8ぴ0に
加熱蝿洋を続けて、反応を終了する。生成した金属石け
んを乾燥し白色細粒状の製品を得る。製品の遊離脂肪酸
量は0.8%である。比較例 1 ステアリン酸20碇部を反応器に仕込み、加熱溶融して
、80qoに調整する。
To this, 35 parts of magnesium oxide is added and uniformly dispersed, and then 35 parts of 500% water is gradually added. At this time, slight foaming is observed. After the addition, heating was continued for 10 minutes at 75-80°C to complete the reaction. The produced metallic soap is dried to obtain a white fine granular product. The free fatty acid content of the product is 0.8%. Comparative Example 1 20 parts of stearic acid was charged into a reactor, heated and melted, and adjusted to 80 qo.

これに酸化カルシウム24部を添加し、均一に分散させ
た後、7000の熱水77部を徐々に添加すると直ちに
急激な発泡が起り、その体積は原液の5倍に達し、その
後固化する。熱泳の添加後10分間加熱鷹拝を続けて、
反応を終了する。生成した金属石けんは固い塊状であり
、これを乾燥粉砕して製品とする。製品の遊離脂肪酸は
1.2%である。比較例 2 ステアリン酸20碇都を反応器に仕込み、加熱溶融して
、80ooに調整する。
After adding 24 parts of calcium oxide and uniformly dispersing it, 77 parts of 7,000 ml hot water was gradually added to it, and rapid foaming immediately occurred, the volume of which reached five times that of the original solution, and then solidified. After adding the hot water, continue heating the water for 10 minutes.
Terminate the reaction. The produced metallic soap is in the form of a hard lump, which is dried and ground into a product. The free fatty acid content of the product is 1.2%. Comparative Example 2 20 tons of stearic acid was charged into a reactor, heated and melted to adjust to 80 oo.

これに酸化マグネシウム18.5部を添加し、均一に分
散させた後、70こ0の熱水10碇部を徐々に添加する
と直ちに急激な発泡が起り、その体積は原液の5倍に達
し、その後固化する。熱水の添加後1び分間加熱燈拝を
続けて反応を終了する。生成した金属石けんは固い塊状
であり、これを乾燥粉砕して製品とする。製品の遊離脂
肪酸は1.3%である。比較例 3 ステアリン酸20の部を反応器に仕込み、加熱、溶融し
て95℃に調整する。
After adding 18.5 parts of magnesium oxide and uniformly dispersing it, 10 parts of 70% hot water were gradually added, and rapid foaming immediately occurred, the volume of which reached five times that of the original solution. It then solidifies. After adding hot water, heating was continued for 1 minute to complete the reaction. The produced metallic soap is in the form of a hard lump, which is dried and ground into a product. The free fatty acid content of the product is 1.3%. Comparative Example 3 20 parts of stearic acid is charged into a reactor and heated to melt and adjust to 95°C.

これに、酸化カルシウム24部を添加し、均一に分散さ
せた後、1000の冷水13部を添加すると、径4〜5
伽のブロック状の反応物が生成する。これを乾燥、粉砕
して製品とする。製品の遊離脂肪酸は10%である。比
較例 4 ステアリン酸20礎都を反応器に仕込み、加熱溶融して
95午0に調整する。
After adding 24 parts of calcium oxide and uniformly dispersing it, adding 13 parts of 1000 ml of cold water,
A block-shaped reactant is generated. This is dried and crushed to make a product. The free fatty acid content of the product is 10%. Comparative Example 4 20% stearic acid was charged into a reactor, heated and melted to adjust the temperature to 95:00.

Claims (1)

【特許請求の範囲】[Claims] 1 炭素数6ないし22を有する高級脂肪酸を融点より
5〜20℃高い温度で溶融させ、これに酸化亜鉛、酸化
カドミウム、酸化錫、酸化鉛、酸化鉄、酸化マグネシウ
ム、酸化カルシウム、酸化バリウム、水酸化亜鉛、水酸
化カドミウム、水酸化カルシウム、水酸化錫、水酸化バ
リウム、水酸化マグネシウム及び水酸化鉛からなる群よ
り選ばれた1種又は2種以上の金属酸化物又は金属水酸
化物を均一に分散させた後、水温5〜55℃の水で脂肪
酸に対し2.5〜40モルの割合で添加し、反応せしめ
ることを特徴とする金属石けんの製造方法。
1. A higher fatty acid having 6 to 22 carbon atoms is melted at a temperature 5 to 20°C higher than its melting point, and zinc oxide, cadmium oxide, tin oxide, lead oxide, iron oxide, magnesium oxide, calcium oxide, barium oxide, and water are added to this. One or more metal oxides or metal hydroxides selected from the group consisting of zinc oxide, cadmium hydroxide, calcium hydroxide, tin hydroxide, barium hydroxide, magnesium hydroxide, and lead hydroxide are uniformly mixed. 1. A method for producing metal soap, which comprises dispersing the soap in water at a temperature of 5 to 55° C. and adding the fatty acid at a ratio of 2.5 to 40 mol to the fatty acid to cause a reaction.
JP5511076A 1976-05-14 1976-05-14 Metal soap manufacturing method Expired JPS6012337B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5511076A JPS6012337B2 (en) 1976-05-14 1976-05-14 Metal soap manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5511076A JPS6012337B2 (en) 1976-05-14 1976-05-14 Metal soap manufacturing method

Publications (2)

Publication Number Publication Date
JPS52138506A JPS52138506A (en) 1977-11-18
JPS6012337B2 true JPS6012337B2 (en) 1985-04-01

Family

ID=12989601

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5511076A Expired JPS6012337B2 (en) 1976-05-14 1976-05-14 Metal soap manufacturing method

Country Status (1)

Country Link
JP (1) JPS6012337B2 (en)

Also Published As

Publication number Publication date
JPS52138506A (en) 1977-11-18

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