JPS6129999B2 - - Google Patents
Info
- Publication number
- JPS6129999B2 JPS6129999B2 JP53097894A JP9789478A JPS6129999B2 JP S6129999 B2 JPS6129999 B2 JP S6129999B2 JP 53097894 A JP53097894 A JP 53097894A JP 9789478 A JP9789478 A JP 9789478A JP S6129999 B2 JPS6129999 B2 JP S6129999B2
- Authority
- JP
- Japan
- Prior art keywords
- sodium
- cleaning
- ethylene oxide
- weight
- sodium percarbonate
- 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
Links
Landscapes
- Detergent Compositions (AREA)
Description
本発明は新規な洗浄漂白剤組成物、更に詳しく
は過炭酸ナトリウム、炭酸ナトリウムおよび特定
の非イオン活性剤を含有する洗浄漂白剤組成物に
関する。
従来、陶器等の固体表面に頑固に付着した汚れ
は、通常の界面活性剤を主剤とする食器用洗浄剤
では脱落せず十分な洗浄効果が得られないので、
次亜塩素酸ナトリウムのような酸化剤を用いて化
学的に漂白していた。しかしながら次亜塩素酸ナ
トリウムで漂白すると、使用中のみならず特有な
塩素臭が残留し、使用者に不快感を与えることが
少なくなく、斯る欠点のない洗浄漂白剤の開発の
ための研究が行われている。
次亜塩素酸ナトリウムにかわる洗浄漂白剤の基
剤として、過炭酸ナトリウム(Na2CO3・3/2
H2O2)、過ホウ酸ナトリウム(NaBO3・
4H2O2)、過酸化トリポリリン酸ナトリウム
(Na5P3O10・H2O2)、過酸化ピロリン酸ナトリウ
ム(Na4P2O7・2H2O2)、硫酸ナトリウム/塩化
ナトリウム/過酸化水素付加体(4Na2SO2・
2H2O2・NaCl)等の過酸化化合物が提案されて
いるが、就中漂白性能上過炭酸ナトリウムが注目
されている。然し乍ら、過炭酸ナトリウムにアル
カリ剤としての炭酸ナトリウム、更に非イオン活
性剤を併有すれば、これも経時的に異臭を発生し
商品価値を著しく低下させる欠点がある。
そこで、本発明者らはこの過炭酸ナトリウムを
含有する洗浄漂白剤組成物のもつ上記欠点を改善
すべく鋭意検討を行つた結果、過炭酸ナトリウム
および炭酸ナトリウムに平均炭素数12〜22個の直
鎖あるいは分岐鎖を有する長鎖アルコールにエチ
レンオキサイドを平均10モル以上付加させた非イ
オン活性剤を併有すれば異臭の発生のないものが
得られることを見出し、本発明を完成した。
すなわち、本発明は(A)過炭酸ナトリウム、(B)炭
酸ナトリウムおよび(C)上記非イオン活性剤を含有
する異臭の発生しない洗浄漂白剤組成物を提供す
るものである。
本発明は非イオン活性剤においてエチレンオキ
サイドの平均付加モル数が10モル未満のものは経
時的に異臭が発生し、また上記以外のエチレンオ
キサイドを付加した非イオン活性剤、例えばポリ
エチレングリコール脂肪酸エステル、ソルビタン
脂肪酸エステルのエチレンオキサイド付加物等も
経時的に異臭が発生して好ましくない。非イオン
活性剤は洗浄漂白剤組成物に対して0.5〜3重量
%(以下単に%と記載する)、特に1〜2.5%配合
するのが好ましい。0.5%未満では洗浄効果が不
十分であり、また3%をこえる配合では洗浄効果
はこれ以上に増大しないばかりか、却つて配合系
の粘着性が増大し、配合組成物の流動性が低下す
るので好ましくない。
洗浄漂白剤組成物の基剤である過炭酸ナトリウ
ムは組成物に対して70%以下では漂白効果に低下
の傾向が認められるため70〜95%、特に75〜90%
配合するのが好ましい。
また炭酸ナトリウムは過炭酸ナトリウムと相乗
的に漂白作用を改善するが、洗浄漂白剤組成物に
対して5〜30%、特に10〜25%配合するのが好ま
しい。本発明における炭酸ナトリウムのかわりに
その類似化合物である炭酸カリウムを使用する
と、吸湿性が増大し高湿条件下、特に夏期におい
て開封放置すると内容物が固まる欠点がある。
本発明の洗浄漂白剤組成物には上記三成分以外
に必要に応じて過酸化水素の安定化剤、例えばケ
イ酸マグネシウム、硫酸マグネシウム、塩化マグ
ネシウム等の水溶性または水不溶性マグネシウム
塩;トリポリリン酸ナトリウム、ピロリン酸ナト
リウム、オルソリン酸ナトリウム等のリン酸塩;
ケイ酸ナトリウム、硫酸ナトリウム等の無機ビル
ダー;エチレンジアミンテトラ酢酸ナトリウム、
ニトリロトリ酢酸ナトリウム等の有機キレート
剤;更に香料、顔料、染料等を添加配合すること
ができる。
次に実施例を挙げて説明する。尚実施例中の%
はすべて重量%を意味する。
実施例 1
過炭酸ナトリウム 80(%)
炭酸ナトリウム 18
直鎖sec.−アルコール(平均炭素数13)エチレン
オキサイド付加物 2
エチレンオキサイド付加モル数のそれぞれ異な
つた非イオン活性剤と他の成分とを上記の組成の
ように配合してなる組成物を、50℃に20日間密封
保存した後、臭いによる官能的評価を行つた。そ
の結果を表1に示す。
The present invention relates to novel cleaning bleach compositions, and more particularly to cleaning bleach compositions containing sodium percarbonate, sodium carbonate, and certain nonionic activators. Conventionally, stains that stubbornly adhere to solid surfaces such as ceramics cannot be removed using ordinary dishwashing detergents based on surfactants, and sufficient cleaning effects cannot be obtained.
They were chemically bleached using oxidizing agents such as sodium hypochlorite. However, when bleaching with sodium hypochlorite, a characteristic chlorine odor remains not only during use but also often causes discomfort to the user, and research is needed to develop a cleaning bleach that does not have such drawbacks. It is being done. Sodium percarbonate (Na 2 CO 3 3/2
H 2 O 2 ), sodium perborate (NaBO 3
4H 2 O 2 ), sodium tripolyphosphate peroxide (Na 5 P 3 O 10・H 2 O 2 ), sodium peroxide pyrophosphate (Na 4 P 2 O 7・2H 2 O 2 ), sodium sulfate/sodium chloride/ Hydrogen peroxide adduct (4Na 2 SO 2
Peroxide compounds such as 2H 2 O 2 .NaCl) have been proposed, but sodium percarbonate is attracting attention because of its bleaching performance. However, if sodium percarbonate, sodium carbonate as an alkali agent, and a nonionic activator are used together, this also has the drawback of generating an unpleasant odor over time and significantly reducing the commercial value. Therefore, the present inventors conducted intensive studies to improve the above-mentioned drawbacks of cleaning and bleaching compositions containing sodium percarbonate, and found that sodium percarbonate and sodium carbonate contain direct carbon atoms with an average carbon number of 12 to 22. The present invention was completed based on the discovery that a nonionic surfactant containing a chain or branched long-chain alcohol with an average of 10 moles or more of ethylene oxide added thereto would produce a product that does not generate off-flavors. That is, the present invention provides a cleaning bleach composition containing (A) sodium percarbonate, (B) sodium carbonate, and (C) the above-mentioned nonionic activator, and which does not generate any off-odor. In the present invention, nonionic surfactants with an average number of moles of ethylene oxide added of less than 10 moles will generate an unpleasant odor over time, and nonionic surfactants with ethylene oxide added other than those mentioned above, such as polyethylene glycol fatty acid esters, Ethylene oxide adducts of sorbitan fatty acid esters are also undesirable because they generate off-flavors over time. The nonionic activator is preferably blended in an amount of 0.5 to 3% by weight (hereinafter simply referred to as %), particularly 1 to 2.5%, based on the cleaning bleach composition. If it is less than 0.5%, the cleaning effect will be insufficient, and if it exceeds 3%, the cleaning effect will not increase any further, and on the contrary, the stickiness of the blended system will increase and the fluidity of the blended composition will decrease. So I don't like it. Sodium percarbonate, which is the base of the cleaning bleach composition, is 70 to 95%, especially 75 to 90%, because if it is less than 70% of the composition, the bleaching effect tends to decrease.
It is preferable to mix them. Sodium carbonate improves the bleaching effect synergistically with sodium percarbonate, but it is preferably added in an amount of 5 to 30%, particularly 10 to 25%, based on the cleaning bleach composition. When potassium carbonate, which is a similar compound thereof, is used in place of sodium carbonate in the present invention, the hygroscopicity increases and the contents tend to harden if left unopened under high humidity conditions, especially in summer. In addition to the above three components, the cleaning bleach composition of the present invention may optionally contain a hydrogen peroxide stabilizer, such as a water-soluble or water-insoluble magnesium salt such as magnesium silicate, magnesium sulfate, or magnesium chloride; sodium tripolyphosphate; , phosphates such as sodium pyrophosphate and sodium orthophosphate;
Inorganic builders such as sodium silicate and sodium sulfate; sodium ethylenediaminetetraacetate,
An organic chelating agent such as sodium nitrilotriacetate; further, fragrances, pigments, dyes, etc. may be added and blended. Next, an example will be given and explained. In addition, % in examples
All values are percentages by weight. Example 1 Sodium percarbonate 80 (%) Sodium carbonate 18 Straight-chain sec.-alcohol (average carbon number 13) Ethylene oxide adduct 2 Nonionic activators with different numbers of added moles of ethylene oxide and other components were prepared as above. After storing the composition in a hermetically sealed manner at 50°C for 20 days, a sensory evaluation based on odor was performed. The results are shown in Table 1.
【表】
実施例 2
一般家庭で長期間使用し茶渋等で汚れた急須を
破砕し、下記組成物0.5%の40℃水溶液に30分間
浸漬する。この表面を柔らかいスポンジで軽くこ
すり、水ですすぎ乾燥した後の汚れの落ち具合い
を判定した。その結果を表2に示す。お浸漬中及
び水洗急須片には塩素臭はもちろん認められなか
つた。[Table] Example 2 A teapot that has been used at home for a long time and is stained with tea stains, etc. is crushed and immersed in a 40°C aqueous solution containing 0.5% of the following composition for 30 minutes. The surface was lightly rubbed with a soft sponge, rinsed with water, and then dried to determine how well the stain had been removed. The results are shown in Table 2. Of course, no chlorine odor was observed in the teapot pieces during soaking or washing.
【表】
(注) ○ 落ちが完全
× 落ちが不完全
実施例 3
過炭酸ナトリウム75%、炭酸ナトリウム23%、
硫酸マグネシウム0.5%、ラウリルアルコールエ
チレンオキサイド平均11モル付加物1.5%よりな
る洗浄漂白剤組成物は50℃にて20日間放置の後も
異臭を認めなかつた。[Table] (Note) ○ Complete fall
× Incomplete removal Example 3 Sodium percarbonate 75%, sodium carbonate 23%,
A cleaning bleach composition consisting of 0.5% magnesium sulfate and 1.5% lauryl alcohol ethylene oxide adduct with an average of 11 moles exhibited no off-odor even after being left at 50°C for 20 days.
Claims (1)
量%、(B)炭酸ナトリウム5〜30重量%及び(C)平均
炭素数12〜22の直鎖または分岐鎖をもつ長鎖アル
コールにエチレンオキサイドを平均10モル以上付
加した非イオン活性剤0.5〜3重量%を含有する
洗浄漂白剤組成物。1. The following essential ingredients: (A) 70-95% by weight of sodium percarbonate, (B) 5-30% by weight of sodium carbonate, and (C) a long-chain alcohol with an average carbon number of 12-22, straight or branched. A cleaning bleach composition containing 0.5 to 3% by weight of a nonionic activator to which 10 moles or more of ethylene oxide is added on average.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9789478A JPS5525435A (en) | 1978-08-11 | 1978-08-11 | Washing and bleaching agent composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9789478A JPS5525435A (en) | 1978-08-11 | 1978-08-11 | Washing and bleaching agent composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5525435A JPS5525435A (en) | 1980-02-23 |
| JPS6129999B2 true JPS6129999B2 (en) | 1986-07-10 |
Family
ID=14204447
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9789478A Granted JPS5525435A (en) | 1978-08-11 | 1978-08-11 | Washing and bleaching agent composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5525435A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6153396A (en) * | 1984-08-22 | 1986-03-17 | 花王株式会社 | Foamable detergent composition |
| JPS62253697A (en) * | 1986-04-02 | 1987-11-05 | 花王株式会社 | Bleaching composition |
-
1978
- 1978-08-11 JP JP9789478A patent/JPS5525435A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5525435A (en) | 1980-02-23 |
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