JPS61141609A - Production of stable foamable composition - Google Patents

Production of stable foamable composition

Info

Publication number
JPS61141609A
JPS61141609A JP59263626A JP26362684A JPS61141609A JP S61141609 A JPS61141609 A JP S61141609A JP 59263626 A JP59263626 A JP 59263626A JP 26362684 A JP26362684 A JP 26362684A JP S61141609 A JPS61141609 A JP S61141609A
Authority
JP
Japan
Prior art keywords
acid
carbon dioxide
water
dioxide gas
bicarbonate
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
Application number
JP59263626A
Other languages
Japanese (ja)
Other versions
JPH0422197B2 (en
Inventor
Tadao Matsumoto
忠雄 松本
Yasushi Wada
康 和田
Tadaaki Sato
佐藤 忠昭
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP59263626A priority Critical patent/JPS61141609A/en
Publication of JPS61141609A publication Critical patent/JPS61141609A/en
Publication of JPH0422197B2 publication Critical patent/JPH0422197B2/ja
Granted legal-status Critical Current

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  • Cosmetics (AREA)
  • Carbon And Carbon Compounds (AREA)
  • Detergent Compositions (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To obtain a foamable composition having high storability and soluble rapidly in water generating carbon dioxide gas bubbles, by contacting carbon dioxide gas with a water-soluble carbonate, bicarbonate, or with a mixture containing both salts and an organic acid solid at normal temperature, and molding the reaction product. CONSTITUTION:A water-soluble carbonate, bicarbonate, or a mixture containing both salts and an organic acid which is solid at normal temperature is made to contact with carbon dioxide gas, and the product is molded to obtain the objective foamable composition. The carbonate and bicarbonate are sodium or potassium salt, and the organic acid is tartaric acid, oxalic acid, citric acid, succinic acid, malic acid or their mixture.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、保存性がよく、かつ水中で炭酸ガスを発泡し
つつ速やかに溶解する発泡性組成物の製造方法に関する
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for producing a foamable composition that has good storage stability and rapidly dissolves carbon dioxide gas in water while foaming.

〔従来の技術〕[Conventional technology]

炭酸塩または/および重炭酸塩と有機酸とを含む混合物
を打錠または造粒等によって成型して発泡性組成物とす
ることは、洗浄剤、漂白剤、ゾール用殺菌剤、浴剤、風
呂水清浄剤等の製品に適用されている。そしてこれらの
製品は水に投入すると、その成分が反応して炭酸ガスを
発生し、速やかに溶解する利点を有すると同時に、消費
者に快適な使用感を与えるので閤品価値を高める効果が
あり、特に浴剤においては、発生する炭酸ガスの血行促
進効果が積嘆的く利用されている。
Forming a mixture containing a carbonate or/and bicarbonate and an organic acid into an effervescent composition by tabletting or granulation can be used as a detergent, bleach, disinfectant for sol, bath agent, bath salt, etc. It is applied to products such as water purifiers. When these products are added to water, their components react and generate carbon dioxide gas, which has the advantage of quickly dissolving the product. At the same time, it provides consumers with a comfortable feeling of use, which has the effect of increasing the value of the food product. Especially in bath additives, the blood circulation promoting effect of the carbon dioxide gas generated is extensively utilized.

〔発明が解決しようとする間@点〕[While the invention is trying to solve the problem @ point]

しかしながら、炭酸塩または/および重炭酸塩と有機酸
とを共存させると、微量の水分で反応が起きるので、炭
酸ガスの発生により包@荏器の内圧が高まり、容器が膨
れ之り、場合によっては破損を引き起こすことがある。
However, when carbonate and/or bicarbonate coexist with an organic acid, a reaction occurs even with a small amount of water, so the internal pressure of the container increases due to the generation of carbon dioxide gas, causing the container to swell and, in some cases, may cause damage.

そしてこのような事帽が発生すると、商品価値が著しく
損なわれるばかりでなく、消費者の1g用をも失墜する
恐れが多分にあつfC,Q炭酸塩あるいは重炭酸塩と有
機#1を混合してしかも安定な製品を得る為には、水分
の混入を徹底的に防ぐことが最も直壁である。そこで製
造時に原料及び工程の管理を厳重に行い、水分の混入を
防ぐことに注意が払われ、更に製造してから消費者が使
用する迄安全に保つ為に密封包装をし、製品の吸湿を防
いでいる。それにも拘わらず、問題は完全には解決され
ていないつ 良く知られている様に、炭酸塩、特に一般に良く用いら
れるナトリウム塩は空気中の水分を吸収して、容易に一
水塩になる。炭酸ナトリウムの一水塩は常温で相対温度
約20%に相当する水蒸気圧を持ち、この水蒸気が製品
中の炭酸塩あるいは重炭酸塩と有機酸との接触点く凝縮
すれば、反応を始めることになる。しかしながら結晶水
を取り除くためには100℃以上に加熱するか、湿度2
0%以下にして放置しなければならないが、このような
対策を取るのは経済的に得策とは言い難い。
If such a problem occurs, not only will the product value be significantly impaired, but there is also a high risk that consumers will lose their interest in 1g. Moreover, in order to obtain a stable product, it is most important to thoroughly prevent the contamination of moisture. Therefore, raw materials and processes are strictly controlled during manufacturing, and attention is paid to preventing moisture from entering the product.Furthermore, after manufacturing, the product is sealed and packaged to keep it safe until it is used by consumers, to prevent moisture absorption. Preventing. Nevertheless, the problem has not been completely solved.As is well known, carbonates, especially the commonly used sodium salts, absorb moisture from the air and easily turn into monohydrates. . Sodium carbonate monohydrate has a water vapor pressure equivalent to about 20% of the relative temperature at room temperature, and if this water vapor condenses at the point of contact between the carbonate or bicarbonate in the product and the organic acid, a reaction will begin. become. However, in order to remove crystal water, it is necessary to heat the water to 100℃ or higher, or to remove it at a humidity of 2.
It is necessary to keep it below 0% and leave it alone, but it is hard to say that it is economically advisable to take such measures.

また重炭酸塩は分解して炭酸塩、炭酸ガス、水を生成し
、紹果的に上記の問題に帰着する。
In addition, bicarbonate decomposes to produce carbonate, carbon dioxide gas, and water, resulting in the above problem.

従って、従来、発泡性組成物を製造する場合には、上記
炭酸塩及び重炭酸塩は勿論、有機酸及びその他の原料中
の水分を完全に取り除くことが必要であり、これがその
製造を煩雑としていた。
Therefore, conventionally, when producing foamable compositions, it is necessary to completely remove the water in the organic acids and other raw materials as well as the carbonates and bicarbonates, which makes the production complicated. there was.

〔問題点を解決するための手段〕[Means for solving problems]

そこで、本発明者らは斯かる問題点を克服すべく鋭意研
究を行つ7t[果、炭酸塩、炭酸ガス及び水の各−分子
から二分子の重炭酸塩が得られることに一層目し、炭酸
塩または/および重炭酸塩と有機酸?:含む混合物に炭
酸ガスを接触させて水を化学的に変化させて系内から水
分を除去し、製品の安定化を図ることに成功し、本発明
を完成した。
Therefore, the inventors of the present invention have conducted intensive research in order to overcome such problems. , carbonates or/and bicarbonates and organic acids? : We succeeded in stabilizing the product by bringing the mixture containing carbon dioxide into contact with it to chemically change the water and remove water from the system, thereby completing the present invention.

従って、本発明は水溶性の炭酸塩または/および重炭酸
塩と常温で固体の有機酸とを含む混合物を炭酸ガスと接
触させ友後、成型することを特徴とする発泡性組成物の
製造方法を提供するものである。
Therefore, the present invention provides a method for producing a foamable composition, which comprises bringing a mixture containing a water-soluble carbonate or/and bicarbonate and an organic acid that is solid at room temperature into contact with carbon dioxide gas, and then molding the mixture. It provides:

本発明において、水溶性の炭酸塩及び重炭酸塩は、それ
ぞれ単独でもまた併用してもよい。これらの対イオンは
ナトリウム、カリウムなどから4ばれる。有機酸として
は常温で固体である酒石酸、蓚酸、クエン酸、コI゛り
酸、リンゴ酸などの中から選ばれたla[または2種以
上のものが使用される。その池の成分としては、実質的
に水分を含まないかあるいは50℃以下、望ましくは1
00℃以下で結晶水を遊離しない有機または無機化合物
が使用される。
In the present invention, water-soluble carbonates and bicarbonates may be used alone or in combination. These counterions include sodium, potassium, and the like. As the organic acid, one selected from tartaric acid, oxalic acid, citric acid, chlorinated acid, malic acid, etc., which are solid at room temperature, or two or more thereof is used. The composition of the pond should be substantially water-free or below 50°C, preferably 1°C.
Organic or inorganic compounds are used that do not liberate water of crystallization at temperatures below 00°C.

本発明方法において、上記成分を含む混合物と炭酸ガス
との接触は成型工程の前、例えば混合機中、混合機と成
型機の間に設けた貯槽中、あるいは移送過程で行われる
。接触させる炭酸ガスの量は当該混合物に対し容積で2
倍以上であるのが好ましい。接触の方法は、固体粒子充
填層、移動゛−1流動層の何れでもよい。
In the method of the present invention, the mixture containing the above components is brought into contact with carbon dioxide gas before the molding step, for example, in a mixer, in a storage tank provided between the mixer and the molder, or during the transfer process. The amount of carbon dioxide to be brought into contact with the mixture is 2 by volume.
It is preferable that it is twice or more. The contacting method may be either a solid particle packed bed or a moving 1 fluidized bed.

斯くして炭酸ガスと接触させ九混合物は、打錠、造粒等
の通常の方法によって成型して製品とする。この混合物
は炭酸ガスと接触後成型されるまでは大気からの吸湿を
できるだけ避けるのが好ましく、更に成型した製品は密
封包装して保存する。
The mixture thus brought into contact with carbon dioxide gas is molded into a product by a conventional method such as tableting or granulation. It is preferable to prevent this mixture from absorbing moisture from the atmosphere as much as possible after it comes into contact with carbon dioxide gas and until it is molded, and the molded product is stored in sealed packaging.

〔実施例〕〔Example〕

以下に本発明の実施例及び試験例を示すが、本発明はこ
れらに限定されるものではない。
Examples and test examples of the present invention are shown below, but the present invention is not limited thereto.

実施例1 重炭酸ナトリウム30重量%(以下単に%と示す)、炭
酸ナトリウム20%、コハク酸40%、芒硝6,3%、
?ジエチレングリコール3.5%および香料0.2%か
らなる混合物10KPf:ナウターミキサ−〔ホンカワ
ミクロンm14  Nx−8m、容積30j〕K投入し
た。
Example 1 Sodium bicarbonate 30% by weight (hereinafter simply referred to as %), sodium carbonate 20%, succinic acid 40%, Glauber's salt 6.3%,
? 10 KPf of a mixture consisting of 3.5% diethylene glycol and 0.2% fragrance was charged into a Nauta mixer [Honkawa Micron m14 Nx-8m, volume 30j]K.

ナウターミキサ−の下部に取り付は九ガス吹込ノズルか
ら、純炭酸ガスt 3 Nj/minの流量で吹き込み
ながらlO分間混合した。なお、混合した粉体の見掛比
重は0.8;M/−であった。次にこの粉末を16メツ
シユの篩を用いて篩分けして粗粒を除い友後、打錠機〔
マシーナ■製DC−WD型〕で4Of/鏑になる様に打
錠し、発泡性錠剤をrA!I!!した。これを?リゾロ
ピレン上にアルミ箔を軍ね、さらに?リエチレンテレフ
タレートでラミネ−)L。
Mixing was carried out for 10 minutes while blowing pure carbon dioxide gas at a flow rate of t 3 Nj/min from a gas blowing nozzle attached to the bottom of the Nauta mixer. The apparent specific gravity of the mixed powder was 0.8; M/-. Next, this powder was sieved using a 16-mesh sieve to remove coarse particles, and then pressed into a tablet machine.
Compress the effervescent tablets with a DC-WD model made by Masina ■ to a ratio of 4 of 1/2 to 100%. I! ! did. this? Also, put aluminum foil on top of the lysopyrene? Laminated with polyethylene terephthalate)L.

たフィルムを使った袋に入れ、ヒートシーラーにより完
全密封包装した。
The product was placed in a bag made of plastic film and completely sealed using a heat sealer.

実施例2 実施例1において、純炭酸ガスの吹込流量を25 N/
/minに増加した以外は同様に操作して発泡性錠剤を
調製し、実施例1と同様にして密封包装し念。
Example 2 In Example 1, the flow rate of pure carbon dioxide gas was changed to 25 N/
Effervescent tablets were prepared in the same manner as in Example 1, except that the effervescent tablet was increased to /min, and sealed and packaged in the same manner as in Example 1.

実施例3 実施例1と同じ配合量の原料粉末をナウターミキサーに
より10分間混合した後、打錠機へ移送する前にいった
ん容積30Jの円錐状ホツノ9−に貯えた。その際、貯
えられた粉体層内へ差し込んだ/Qイデを通して、純炭
酸ガスを3Nj/minの流量で30分間吹き込んだ。
Example 3 Raw material powders in the same amount as in Example 1 were mixed for 10 minutes using a Nauta mixer, and then stored in a conical hotpot 9- with a volume of 30 J before being transferred to a tablet press. At that time, pure carbon dioxide gas was blown at a flow rate of 3 Nj/min for 30 minutes through a Qide inserted into the stored powder bed.

以下、実施例1と同様に篩分け、打錠し、密封包装した
Thereafter, the mixture was sieved, tableted, and sealed in the same manner as in Example 1.

比較例 実施例1において、純炭酸ガスを吹き込まない以外は同
様に操作して発泡性錠剤を調製した。
Comparative Example An effervescent tablet was prepared in the same manner as in Example 1, except that pure carbon dioxide gas was not blown into the tablet.

試験例 実施例1〜3及び比較例でrA製した発泡性錠剤につい
て、その安定性を試験した。
Test Example The effervescent tablets manufactured by rA in Examples 1 to 3 and Comparative Example were tested for stability.

錠剤の安定性を評価する試験方法は、包装品10個を、
50℃の恒温槽内に24時間放置し、その前後の各サン
プルの体積変化を測定し、平均イ直をとり、体積変化の
少ないもの程安定性が高いと判断する方法をとった。こ
の除、体積変化を正確に測定するため電子上皿天秤に水
槽(容積31)′f、のせ、包装された錠剤全水槽に沈
めることにより増加した体積分の水の重量変化を測定す
る方法を使用したうその結果は第1表のとおりであるう *n=l0 〔効 果〕 第1表の安定性試域の結果から明らかな如く、本発明に
より、成型前に炭酸ガスと接触させて得られる発泡性組
成物は、従来法によって得られるものに比較し、保存中
における体積増加が少なく、極めて安定であった。
The test method for evaluating the stability of tablets is to test 10 packaged products by
The sample was left in a constant temperature bath at 50° C. for 24 hours, the volume change of each sample was measured before and after that, the average value was taken, and the smaller the volume change, the higher the stability. In order to accurately measure the change in volume, we used a method of placing a water tank (volume 31)'f on an electronic balance and submerging all the packaged tablets in the water tank to measure the weight change of the increased volume of water. The results of the tests used are shown in Table 1. *n=l0 [Effects] As is clear from the results of the stability test range in Table 1, the present invention allows molding to be brought into contact with carbon dioxide gas before molding. The resulting foamable composition exhibited less volume increase during storage and was extremely stable compared to those obtained by conventional methods.

以上that's all

Claims (1)

【特許請求の範囲】 1、水溶性の炭酸塩または/および重炭酸塩と常温で固
体の有機酸とを含む混合物を炭酸ガスと接触させた後、
成型することを特徴とする発泡性組成物の製造方法。 2 炭酸塩および重炭酸塩がナトリウムまたはカリウム
塩である特許請求の範囲第1項記載の製造方法。 3 有機酸が酒石酸、蓚酸、クエン酸、コハク酸および
リンゴ酸の中から選ばれた1種または2種以上のもので
ある特許請求の範囲第1項記載の製造方法。
[Claims] 1. After contacting a mixture containing a water-soluble carbonate or/and bicarbonate and an organic acid that is solid at room temperature with carbon dioxide gas,
A method for producing a foamable composition, the method comprising molding the composition. 2. The manufacturing method according to claim 1, wherein the carbonate and bicarbonate are sodium or potassium salts. 3. The manufacturing method according to claim 1, wherein the organic acid is one or more selected from tartaric acid, oxalic acid, citric acid, succinic acid, and malic acid.
JP59263626A 1984-12-13 1984-12-13 Production of stable foamable composition Granted JPS61141609A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59263626A JPS61141609A (en) 1984-12-13 1984-12-13 Production of stable foamable composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59263626A JPS61141609A (en) 1984-12-13 1984-12-13 Production of stable foamable composition

Publications (2)

Publication Number Publication Date
JPS61141609A true JPS61141609A (en) 1986-06-28
JPH0422197B2 JPH0422197B2 (en) 1992-04-15

Family

ID=17392130

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59263626A Granted JPS61141609A (en) 1984-12-13 1984-12-13 Production of stable foamable composition

Country Status (1)

Country Link
JP (1) JPS61141609A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015134728A (en) * 2014-01-17 2015-07-27 日本曹達株式会社 Slimicide for piping having traps and slime control method using same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015134728A (en) * 2014-01-17 2015-07-27 日本曹達株式会社 Slimicide for piping having traps and slime control method using same

Also Published As

Publication number Publication date
JPH0422197B2 (en) 1992-04-15

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