JPS58140312A - Stable composition for generating gaseous carbon dioxide - Google Patents
Stable composition for generating gaseous carbon dioxideInfo
- Publication number
- JPS58140312A JPS58140312A JP57020570A JP2057082A JPS58140312A JP S58140312 A JPS58140312 A JP S58140312A JP 57020570 A JP57020570 A JP 57020570A JP 2057082 A JP2057082 A JP 2057082A JP S58140312 A JPS58140312 A JP S58140312A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- composition
- carbonate
- zeolite
- carbon dioxide
- 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
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Carbon And Carbon Compounds (AREA)
Abstract
Description
【発明の詳細な説明】 本発明は安定な炭酸ガス発生組成物に関する。[Detailed description of the invention] FIELD OF THE INVENTION This invention relates to stable carbon dioxide generating compositions.
炭酸塩と酸を混合すると炭酸ガスが発生するととはよく
知られている事実である。この現象は粉末清涼飲料水、
義歯用洗浄鋼或いは風呂水清浄鋼部に使用されている。It is a well-known fact that carbon dioxide gas is produced when carbonates and acids are mixed. This phenomenon occurs in powdered soft drinks,
Used in denture cleaning steel or bath water cleaning steel.
これらの商品は固形の炭酸塩と固形の酸の温合物である
。炭酸ガスの発生する激しさは酸及び炭酸塩の一度が高
い程よい。粉末清涼飲料用粉末ジュース或いは義歯用洗
浄剤の場合、使用する水の量は少ない為に粉末或いは顆
粒同志の混合系でもよく発泡する。しかしながら多量の
水に添加すゐ風呂水清浄剤の如禽紘粉末同志の混合では
発泡性は十分でなく、錠剤で添加するのが好tしい。し
かしながら錠剤の場合、炭酸塩と酸の接触性が^まるの
で長期保存すると発泡性が低下してくる。These products are warm mixtures of solid carbonates and solid acids. The intensity with which carbon dioxide gas is generated is better as the ratio of acid and carbonate is higher. In the case of powdered juice for powdered soft drinks or cleaning agents for dentures, since the amount of water used is small, even a mixed system of powders or granules foams well. However, mixing the powdered bathwater cleanser with a large amount of water does not provide sufficient effervescence, so it is preferable to add it in the form of tablets. However, in the case of tablets, the contact between carbonate and acid decreases, so the effervescence decreases when stored for a long period of time.
本発明者らはかかる!i泡性の低下を防止すべく鋭意検
討し九結果、ゼオライトを添加することによシ解決し得
ることを見い出し本発明に到達し九。The inventors take it! We conducted extensive studies to prevent the deterioration of foamability, and as a result, we discovered that the problem could be solved by adding zeolite, resulting in the present invention.
即ち、本発明は必須成分として、炭酸塩、固形又は粉末
状酸及びゼオライトを含むことを特徴とする安定な炭酸
ガス発生組成物を提供するものである。That is, the present invention provides a stable carbon dioxide gas-generating composition characterized by containing a carbonate, a solid or powdered acid, and a zeolite as essential components.
本発明に使用される炭酸塩としては重炭酸ナトリウム、
重炭酸カリウムが最も好ましいが、炭酸ナトリウム、炭
酸カリウムも使用出来る。Carbonates used in the present invention include sodium bicarbonate,
Potassium bicarbonate is most preferred, but sodium carbonate and potassium carbonate can also be used.
本発明に用いられる酸としては酒石酸、クエン酸、コハ
ク酸、フマール酸、マレイン酸、リンゴ酸等々の有機酸
が挙げられる。本発明において、ゼオライトとしては天
然産出ゼオライト。Examples of acids used in the present invention include organic acids such as tartaric acid, citric acid, succinic acid, fumaric acid, maleic acid, and malic acid. In the present invention, the zeolite is a naturally occurring zeolite.
合成ゼオライトいづれ4使用出来るが、好ましくは合成
ゼオライトがよい1本発明で用いられる合成ゼオライト
としては%lC次の(!)式で示されるアル建ノケイ酸
塩が好ましい。Any synthetic zeolite can be used, but synthetic zeolites are preferred.The synthetic zeolites used in the present invention are preferably alkyl silicates represented by the following formula (!).
(M、no)X・ムj20.−(810,)ア
(夏)〔y工0.6〜10
ゼオライトは結晶構造中に結晶水を持つが、本発明で用
いるゼオライトは結晶水を持っていてもよいが、好まし
くは飽和結晶水以下の水分、より好ましくは実質的に水
分を含まないゼオライトがよい。(M, no) X Muj20. -(810,)a
(Summer) [y 0.6 to 10 Zeolite has crystal water in its crystal structure, and the zeolite used in the present invention may have crystal water, but the water content is preferably less than saturated crystal water, and more preferably A zeolite containing substantially no water is preferable.
本発明組成物中の炭酸塩と酸との配合割合は重量比で?
!I−5:5〜!5が好壕しく、!S〜30:s〜70
が更に好ましい。又ゼオライトの配合割合は炭酸塩と酸
の混合物に対しO6S〜50重量慢が好★しく、2〜S
O重量憾が更に好ましい。50重重量上り多く添加して
もさしつかえないが、不溶分が多くな勤好ましくない。What is the weight ratio of carbonate and acid in the composition of the present invention?
! I-5:5~! 5 is a good moat! S~30:s~70
is even more preferable. Also, the blending ratio of zeolite is preferably O6S to 50% by weight relative to the mixture of carbonate and acid, and 2 to S
More preferred is O weight. Although it is acceptable to add more than 50% by weight, it is undesirable because it contains a large amount of insoluble matter.
本発明の組成物には更に必要に応じて**ナトリウム、
トリポリリン酸ナトリウム、ビロリン酸ナトリウム、リ
ン酸ナトリウムの如き無機塩、ポリエチレングリコール
(2000〜20000) 。The composition of the present invention may optionally further include **sodium,
Inorganic salts such as sodium tripolyphosphate, sodium birophosphate, sodium phosphate, polyethylene glycol (2000-20000).
カルボキシメチルセルロース、ヒドロキシエチルセルレ
ースの如き高分子化合物、クエン酸ナトリウム、WA石
酸ナトリウム、コハク酸す″#−1Jウム、マロン駿ナ
トリタナトリウム等々機酸塩、陰イオン性活性剤、非イ
オン性活性剤9両性活性剤、陽イオン性活性剤の如き界
面活性剤、更には少量の香料、顔料、染料等々を任意成
分として添加することが出来る。High molecular compounds such as carboxymethyl cellulose, hydroxyethyl cellulose, sodium citrate, WA sodium chlorate, sodium succinate, sodium marron trita, etc., anionic activators, nonionic Active Agent 9 Surfactants such as amphoteric active agents and cationic active agents, as well as small amounts of fragrances, pigments, dyes, etc., can be added as optional ingredients.
本発明に係る成分の粒度は特に規定するものではないが
、一般には14メツシユ箇(11111を95悌以上通
過する亀のがよく、8oメツシユ篩(177μ3に80
1!以上残るものがよいが。The particle size of the component according to the present invention is not particularly specified, but it is generally good to have particles that pass through a 14-mesh sieve (11111 95 or more), and an 80-mesh sieve (80
1! What remains is better.
80メツシェ篩1oo−通過品でも用いることが出来る
。本発明の組成物は一錠0.5〜Sot好普しくは1〜
1sOfK打錠して風呂水添加剤として用いることが出
来る。It is also possible to use products that pass through a 100-80 Metsche sieve. One tablet of the composition of the invention preferably ranges from 0.5 to 1.
It can be compressed into 1sOfK tablets and used as a bath water additive.
以下11施例において本発明を更に詳細にm@する。The present invention will be described in further detail in the following 11 Examples.
実施例 1
重炭酸ナトリウムと酒石酸にゼオライト(ゼオライト4
ム;商品名ゼオラム4ム)を種々の量添加し1表1に示
すム〜Gの組成物を得九。これらの組成物を一昼夜(1
4時間)ゼオラム4ムを入れたデシケータ−中に保存し
、その後直ちに517錠に打鋺し丸。この錠剤を小孔を
持つ迷路形アルンピロ包*(外部からの水分の吸湿はし
ないが、内部で発生した炭酸ガスは外部に排出される機
構を持つピロ包鋏、夷願昭56−134804号明細書
参照)に−錠づつ懐填し友。50℃に20日間保存しそ
の炭酸ガス発生量の変化を下記の方法により一定し九。Example 1 Zeolite (zeolite 4) in sodium bicarbonate and tartaric acid
(trade name: Zeolum 4) was added in various amounts to obtain the compositions shown in Table 1. These compositions were kept for a day and night (1
4 hours) Stored in a desiccator containing 4 ml of Zeorum, then immediately punched into 517 tablets. This tablet is packed in a labyrinth-shaped alumpyro capsule with small holes* (pyro capsule scissors with a mechanism that does not absorb moisture from the outside but releases the carbon dioxide gas generated inside, specification number 134804/1986). (Refer to the book) - A friend who fills the pocket with locks one by one. It was stored at 50°C for 20 days, and the changes in the amount of carbon dioxide gas produced were kept constant using the following method.9.
結果を表2に示す。The results are shown in Table 2.
炭酸ガス発生量測定法5200@lの三角フラスコに2
S℃の水道水を添加し、その中に錠剤ヲー錠添加してス
ターラービースで攪拌5分後の発生量を一定しえ、一定
KIIIしては錠剤添加と同時に三角フラスコを500
11j容の注射器状容器とポリエチレン細管で連結され
九ゴム楡で書間し、発生する炭酸ガスを注射器に導入し
、ガスによ勤押し上げられ走置をガス発生量としえ。Method for measuring the amount of carbon dioxide gas produced: 2 in a 5200@l Erlenmeyer flask.
Add tap water at S℃, add the tablets into it, stir with a stirrer bead, keep the amount generated after 5 minutes constant, and at the same time add the tablets, add the Erlenmeyer flask to 500ml.
A syringe-shaped container with a capacity of 11j is connected with a polyethylene thin tube and separated by nine rubber elms, and the generated carbon dioxide gas is introduced into the syringe, and the amount of gas generated is defined as the amount of gas generated.
表 1
表 2
実施例 2
表1K示す各種炭酸ガス発生組成物を調製し丸。その際
ゼオライト21’、Y、Lは夫々500℃の電気炉で常
圧で熱部履し冷却したものを用い、夫々の原料は16メ
ツシユ(11111m)〜80メツシュ10.177■
)の間の粒度品を用いた。ヒれらの組成物を5 fAi
I づつ打錠し、実施例1と同様にアルンピロ包装し
、50CK2(1日間保存しその炭酸ガス斃生量を調定
しえ、結果を表4に示す。Table 1 Table 2 Example 2 Various carbon dioxide gas generating compositions shown in Table 1K were prepared. At that time, zeolites 21', Y, and L were each cooled in a hot section at normal pressure in an electric furnace at 500°C, and the raw materials for each were 16 mesh (11111 m) to 80 mesh 10.177 cm.
) was used. 5 fAi of fillet composition
Tablets were compressed into 50CK2 tablets, packaged in Alumpiro packaging in the same manner as in Example 1, and stored for 1 day to determine the amount of carbon dioxide released. The results are shown in Table 4.
表 墨 表 4Front Ink Table 4
Claims (1)
オライトを含むことを特徴とする安定な炭酸ガス発生組
成物。 2、 ゼオライトが実質的に水分を金型ないものである
特許請求の範囲第1項記載の組成物。 5、 固形又は粉末状酸が有機酸である特許請求の範囲
第1項記載の組成物。 4、有機酸が酒石酸、クエン酸、コハク酸、!レイン酸
、フマール駿又はりンゴ酸である特許請求の範囲第5項
記載の組成物。 5、 炭酸塩が重炭酸ナトリウム、重炭酸カリウム、巌
酸ナトリクム又は炭酸カリウムである特許請求の範囲第
1項記載の組成物。 6、 炭酸塩、有機酸及び実質的に水分を會まないゼオ
ライトを含む特許請求の範囲第1項記載の組成物。[Scope of Claims] 1. A stable carbon dioxide gas-generating composition, characterized in that it contains a carbonate, isomorphic or powdered acid, and zeolite as essential components. 2. The composition according to claim 1, wherein the zeolite is substantially free of moisture. 5. The composition according to claim 1, wherein the solid or powdered acid is an organic acid. 4. Organic acids are tartaric acid, citric acid, and succinic acid! The composition according to claim 5, which is leic acid, fumaric acid or malic acid. 5. The composition according to claim 1, wherein the carbonate is sodium bicarbonate, potassium bicarbonate, sodium sulfate, or potassium carbonate. 6. The composition according to claim 1, which contains a carbonate, an organic acid, and a zeolite that does not substantially absorb water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57020570A JPS58140312A (en) | 1982-02-10 | 1982-02-10 | Stable composition for generating gaseous carbon dioxide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57020570A JPS58140312A (en) | 1982-02-10 | 1982-02-10 | Stable composition for generating gaseous carbon dioxide |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58140312A true JPS58140312A (en) | 1983-08-20 |
JPS649241B2 JPS649241B2 (en) | 1989-02-16 |
Family
ID=12030845
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57020570A Granted JPS58140312A (en) | 1982-02-10 | 1982-02-10 | Stable composition for generating gaseous carbon dioxide |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58140312A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0710621A1 (en) * | 1994-11-02 | 1996-05-08 | Rengo Co., Ltd. | Carbon dioxide gas generating compositions |
JP2002501872A (en) * | 1998-02-09 | 2002-01-22 | サウスウエスト・リサーチ・インスティチュート | Silicate containing powder |
WO2004024625A3 (en) * | 2002-09-13 | 2004-07-08 | Ica Trinova Llc | Composition and method for producing carbon dioxide |
JP2009249963A (en) * | 2008-04-09 | 2009-10-29 | Asahi Kasei Construction Materials Co Ltd | Vent pipe embedding apparatus and embedding method |
JP2016141637A (en) * | 2015-01-30 | 2016-08-08 | 関西酵素株式会社 | Compression-molded cosmetic |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11623018B2 (en) | 2020-08-31 | 2023-04-11 | Promethium Limited | Photoactivated semiconductor photocatalytic air purification |
US11612673B2 (en) | 2020-08-31 | 2023-03-28 | Promethium Limited | Photoactivated semiconductor photocatalytic air purification |
-
1982
- 1982-02-10 JP JP57020570A patent/JPS58140312A/en active Granted
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0710621A1 (en) * | 1994-11-02 | 1996-05-08 | Rengo Co., Ltd. | Carbon dioxide gas generating compositions |
JP2002501872A (en) * | 1998-02-09 | 2002-01-22 | サウスウエスト・リサーチ・インスティチュート | Silicate containing powder |
WO2004024625A3 (en) * | 2002-09-13 | 2004-07-08 | Ica Trinova Llc | Composition and method for producing carbon dioxide |
US7347994B2 (en) | 2002-09-13 | 2008-03-25 | Ica Trinova, Llc | Method and composition for attracting arthropods by volatilizing an acid |
US7922992B2 (en) | 2002-09-13 | 2011-04-12 | Ica Trinova, Llc | Composition and method for producing carbon dioxide |
US8709396B2 (en) | 2002-09-13 | 2014-04-29 | Premark Feg L.L.C. | Method and composition for attracting arthropods by volatizing an acid |
JP2009249963A (en) * | 2008-04-09 | 2009-10-29 | Asahi Kasei Construction Materials Co Ltd | Vent pipe embedding apparatus and embedding method |
JP2016141637A (en) * | 2015-01-30 | 2016-08-08 | 関西酵素株式会社 | Compression-molded cosmetic |
Also Published As
Publication number | Publication date |
---|---|
JPS649241B2 (en) | 1989-02-16 |
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