JPH0335359B2 - - Google Patents

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Publication number
JPH0335359B2
JPH0335359B2 JP56199712A JP19971281A JPH0335359B2 JP H0335359 B2 JPH0335359 B2 JP H0335359B2 JP 56199712 A JP56199712 A JP 56199712A JP 19971281 A JP19971281 A JP 19971281A JP H0335359 B2 JPH0335359 B2 JP H0335359B2
Authority
JP
Japan
Prior art keywords
sodium
zeolite
bleach
aluminum
present
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 - Lifetime
Application number
JP56199712A
Other languages
Japanese (ja)
Other versions
JPS58101199A (en
Inventor
Isamu Katagiri
Junosuke Nakagawa
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 JP19971281A priority Critical patent/JPS58101199A/en
Publication of JPS58101199A publication Critical patent/JPS58101199A/en
Publication of JPH0335359B2 publication Critical patent/JPH0335359B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は水溶液中で次亜塩素酸又は次亜塩素酸
塩を生成する粉末塩素系標白剤の安定化組成物に
関する。 次亜塩素酸又は次亜塩素酸塩を水溶液中で生成
する粉末塩素系漂白剤は、その良好な漂白性能、
殺菌性能の故に、家庭用衣類の漂白、浄化槽、プ
ールの殺菌等の用途に使用されており、これら漂
白剤としてはトリクロルイソシアヌール酸、ジク
ロルイソシアヌール酸、ジクロルイソシアヌール
酸カリウム、ジクロルイソシアヌール酸ナトリウ
ム、ジクロロジメチルヒダントイン、テトラクロ
ログルコルリル或いはサラシ粉等がある。 しかし、これら粉末塩素系漂白剤は、保存時の
安定性に乏しく、分解して塩素ガスを発生する。
その結果、刺激臭、アレルギー等、人体への好ま
しくない影響、および包装容器の腐蝕等の不都合
を生じる。そこで、ジクロルイソシアヌール酸、
ジクロルイソシアヌール酸カリウム、ジクロルイ
ソシアヌール酸ナトリウム等が安定性の点で優れ
ている点から、工業的に大量生産されている。し
かし、これらの物質も尚、安定性は十分でないた
め、特定の香料、メラミン等の安定剤を添加する
提案がなされてきた。しかしながら、これら安定
剤を添加しても尚、塩素系漂白剤の安定化は十分
とはいえず、家庭用漂白剤等、大衆消費者のため
の商品には到庭使用できるものではない。たとえ
ば、これら粉末塩素系漂白剤は粉末状で使用して
もよいが、1回の使用分だけ錠剤にして用いると
便利である。これらの錠剤は一錠一錠をアルミニ
ユウム/ポリエチレンラミネート包装しておけば
外部からの吸湿もなく好ましい。しかしながら余
り長期間保存するとアルミニウムが腐蝕を受け小
孔を生成しその後は安定性を低下する様になる。 本発明者らは粉末塩素系漂白剤の安定化につい
て鋭意検討した結果合成結晶型A型ゼオライトを
添加することにより顕著な安定化効果の得られる
ことを見い出し本発明に到達した。 即ち、本発明はジクロルイソシアヌール酸ナト
リウム、ジクロルイソシアヌール酸カリウム及び
ジクロルイソシアヌール酸からなる群からばれた
1種又は2種以上の粉末塩素系漂白剤と、含成結
晶型A型ゼオライトとを重量比で97/3〜70/30
の割合で含有することを特徴とする粉末塩素系漂
白剤の安定化組成物を提供するものである。 本発明に用いられるA型ゼオライトは合成結晶
型で、次の式で示される骨格構造を持つものであ
る。 6{(Na2O)・(Al2O3)・2(SiO2)} ゼオライトは一般的には結晶水を持ち飽和された
状態で3〜25重量%の水分を持つことになる。こ
の様な含水ゼオライトを用いてもよいが、好まし
くは飽和水和水以下の結晶水、更に好ましくは結
晶水を含まないゼオライトがよい。 本発明組成物中の塩素系漂白剤とA型ゼオライ
トとの重量比率は97/3〜70/30の範囲で選択さ
れる。即ちゼオライトの量が少ないと十分効果が
なく、又多くても無駄になるだけである。本発明
の組成物を製造するに当つては特に限定するもの
ではないが粉末塩素系漂白剤、ゼオライトの粒度
を16meshフルイ通過が95%以上のものを用いる
ことが好ましい。 本発明の組成物には更に必要に応じて、硫酸ナ
トリウム、重炭酸ナトリウム、炭酸ナトリウム、
トリボリリン酸ナトリウム、ピロリン酸ナトリウ
ム、リン酸一ナトリウム、リン酸二ナトリウム、
リン酸三ナトリウムの如き希釈剤としての無機
塩、クエン酸ナトリウム、修酸ナトリウム、酒石
酸ナトリウム、コハク酸ナトリウム、ニトリロト
リ酢酸ナトリウム、エチレンジアミン四酢酸ナト
リウム、ポリエチレングリコール(分子量2000〜
20000)、カルボキシメチルセルロースナトリウム
塩、ヒドロキシエチルセルロース、アルキルベン
ゼンスルホン酸ナトリウム、アルキル硫酸ナトリ
ウム、アルキルスルホン酸ナトリウム、ポリエチ
レングリコールアルキルエーテル、ポリエチレン
グリコールアルキルフエノールエーテル等の有機
酸塩、高分子化合物金属キレート剤、陰イオン性
界面活性剤、非イオン性界面活性剤等々、更には
香料、顔料、染料等々、漂白剤、漂白洗剤、浄化
槽殺菌剤、プール用殺菌剤等の用途に対する製品
をつくるための常用成分を添加することができ
る。 以下、、実施例により本発明を更に詳細に説明す
る。尚、例中の部は重量基準である。 実施例 1
The present invention relates to a composition for stabilizing a powdered chlorine whitening agent that produces hypochlorous acid or hypochlorite in aqueous solution. Powdered chlorine bleach that produces hypochlorous acid or hypochlorite in an aqueous solution has good bleaching performance,
Because of its sterilizing properties, it is used for purposes such as bleaching household clothes, sterilizing septic tanks, and swimming pools. These bleaching agents include trichloroisocyanuric acid, dichloroisocyanuric acid, potassium dichloroisocyanurate, and dichloroisocyanurate. Examples include sodium isocyanurate, dichlorodimethylhydantoin, tetrachloroglucoruril, and salami powder. However, these powdered chlorine bleaches have poor stability during storage and decompose to generate chlorine gas.
As a result, undesirable effects on the human body such as irritating odors and allergies, and inconveniences such as corrosion of packaging containers occur. Therefore, dichloroisocyanuric acid,
Potassium dichloroisocyanurate, sodium dichloroisocyanurate, and the like are industrially produced in large quantities because of their excellent stability. However, since these substances still do not have sufficient stability, proposals have been made to add certain fragrances and stabilizers such as melamine. However, even with the addition of these stabilizers, the stabilization of chlorine bleach is still insufficient, and it cannot be used as a commercial product for mass consumers, such as household bleach. For example, these powdered chlorine bleaches may be used in powder form, but it is convenient to form them into tablets for one-time use. It is preferable for these tablets to be packaged one by one in aluminum/polyethylene laminate to avoid moisture absorption from the outside. However, if the aluminum is stored for too long, it will corrode and form small pores, which will subsequently reduce its stability. The inventors of the present invention have conducted extensive studies on the stabilization of powdered chlorine bleach, and have discovered that a significant stabilizing effect can be obtained by adding synthetic crystalline A-type zeolite, thereby achieving the present invention. That is, the present invention provides one or more powdered chlorine bleaches selected from the group consisting of sodium dichloroisocyanurate, potassium dichloroisocyanurate, and dichloroisocyanuric acid, and a crystal type A-containing bleach. Weight ratio of 97/3 to 70/30 with zeolite
The present invention provides a stabilizing composition for powdered chlorine bleach, characterized in that it contains a powdered chlorine bleach in a proportion of . The A-type zeolite used in the present invention is a synthetic crystal type and has a skeleton structure represented by the following formula. 6 {(Na 2 O)・(Al 2 O 3 )・2(SiO 2 )} Zeolite generally has water of crystallization and has a water content of 3 to 25% by weight in a saturated state. Although such a hydrous zeolite may be used, it is preferable to use a zeolite containing no crystal water, preferably less than saturated water of hydration, and more preferably a zeolite containing no crystal water. The weight ratio of chlorine bleach to type A zeolite in the composition of the present invention is selected within the range of 97/3 to 70/30. That is, if the amount of zeolite is small, it will not be sufficiently effective, and if the amount is large, it will just be wasted. In producing the composition of the present invention, although there are no particular limitations, it is preferable to use a powdered chlorine bleach and a zeolite having a particle size of 95% or more that passes through a 16 mesh sieve. The composition of the present invention may further include sodium sulfate, sodium bicarbonate, sodium carbonate,
Sodium tribolyphosphate, sodium pyrophosphate, monosodium phosphate, disodium phosphate,
Inorganic salts as diluents such as trisodium phosphate, sodium citrate, sodium oxalate, sodium tartrate, sodium succinate, sodium nitrilotriacetate, sodium ethylenediaminetetraacetate, polyethylene glycol (molecular weight from 2000 to
20000), carboxymethyl cellulose sodium salt, hydroxyethyl cellulose, sodium alkylbenzene sulfonate, sodium alkyl sulfate, sodium alkyl sulfonate, organic acid salts such as polyethylene glycol alkyl ether, polyethylene glycol alkyl phenol ether, polymer compound metal chelating agent, anion chemical surfactants, nonionic surfactants, etc., as well as fragrances, pigments, dyes, etc., as well as commonly used ingredients to make products for applications such as bleach, bleach detergent, septic tank disinfectant, pool disinfectant, etc. be able to. Hereinafter, the present invention will be explained in more detail with reference to Examples. Note that parts in the examples are based on weight. Example 1

【表】 上記組成を有するA〜Eの5種の混合物を夫々
3gづつ錠剤に打錠し、アルミピロ包装に密封し
て20℃の恒温室に6ケ月間保存し、ピロ包装のア
ルミ面に生じる腐蝕を観察した。夫々のサンプル
30ケづつ保存し、1ケ月に3ケづつ任意に取り出
し包装を破り、内側のアルミの腐蝕を観察した。
結果を表1に示す。
[Table] Compress 3g of each of the five mixtures A to E having the above composition into tablets, seal them in aluminum pillow packaging, and store them in a constant temperature room at 20℃ for 6 months. Corrosion was observed. each sample
I stored 30 pieces at a time, and took out 3 pieces every month at will, tore the packaging, and observed the corrosion of the aluminum inside.
The results are shown in Table 1.

【表】 実施施例 2【table】 Implementation example 2

【表】 A型ゼオライトを種々の水分含量に調整して上
記配合組成を有する組成物を作り3g量づつアル
ミピロ包装に密閉しし6ケ月保存した。実施例1
と同様にアルミ面に生じる腐蝕を観察した。 結果を表2に示す。
[Table] A-type zeolite was adjusted to various moisture contents to prepare compositions having the above compositions, which were sealed in aluminum pyropackaging in 3 g portions and stored for 6 months. Example 1
Corrosion occurring on the aluminum surface was observed in the same manner. The results are shown in Table 2.

【表】 実施例 3【table】 Example 3

【表】 上記組成を有するH〜Kの4種の混合物を1錠
30gの量で3ケ打錠し、扁平円柱状の錠剤をつく
つた。これを500c.c.広口ポリエチレンボトルに密
栓して保存した。6ケ月室温保存後に開詮した。
Hは強い塩素の刺激臭があつたがI〜Kはほとん
ど塩素臭はなかつた。 実施例 4
[Table] 1 tablet of a mixture of 4 types of H to K having the above composition
Three 30g tablets were compressed to produce flat cylindrical tablets. This was stored in a 500 c.c. wide-mouth polyethylene bottle with a tightly stopper. It was opened after being stored at room temperature for 6 months.
H had a strong pungent odor of chlorine, but I to K had almost no chlorine odor. Example 4

【表】 上記の表に示した組成を有するL〜Qの6種の
混合物を夫々3gずつ錠剤に打錠し、アルミピロ
包装に密封して、40℃の恒温室に保存し、ピロ包
装のアルミ面に生ずる腐蝕を観察した。夫々サン
プルを9ケずつ保存し、15日後、30日後、45日後
に3ケずつ任意に取り出し包装を破り、内側のア
ルミの腐蝕を観察した。その結果を上記の表に併
せて示した。 この加速試験は、40℃、45日で20℃、6ケ月の
試験にほぼ相応する。 上表より、合成非晶質ゼオライトを使用した場
合は分解抑止効果はあるが、多量に配合する必要
があるのに対し、本発明で使用する合成結晶型A
型ゼオライトは少量で効果があることがわかる。
また、合成非晶質ゼオライトを使用した場合、打
錠性がよくなかつた。即ち、ある程度の分解抑止
効果を示す組成物O,Pを打錠した錠剤は脆く手
でくだけやすかつた。
[Table] The six mixtures L to Q having the compositions shown in the table above were compressed into tablets of 3 g each, sealed in aluminum pyro packaging, stored in a constant temperature room at 40°C, and placed in aluminum pyro packaging. Corrosion occurring on the surface was observed. Nine samples of each were stored, and after 15, 30, and 45 days, three samples were taken out at will, the packaging was torn, and the corrosion of the aluminum inside was observed. The results are also shown in the table above. This accelerated test is approximately equivalent to a 6-month test at 20°C for 45 days at 40°C. From the table above, it can be seen that when synthetic amorphous zeolite is used, it has the effect of suppressing decomposition, but it needs to be blended in a large amount, whereas synthetic crystal type A used in the present invention
It can be seen that zeolite type is effective in small amounts.
Furthermore, when synthetic amorphous zeolite was used, tableting properties were not good. That is, the tablets obtained by compressing compositions O and P, which exhibit a certain degree of decomposition-inhibiting effect, were brittle and easy to break apart by hand.

Claims (1)

【特許請求の範囲】 1 ジクロルイソシアヌール酸ナトリウム、ジク
ロルイソシアヌール酸カリウム及びジクロルイソ
シアヌール酸からなる群から選ばれた1種又は2
種以上の粉末塩素系漂白剤と、含成結晶型A型ゼ
オライトとを重量比で97/3〜70/30の割合で含
有することを特徴とする粉末塩素系漂白剤の安定
化組成物。 2 A型ゼオライトの水分含量が実質的に0であ
る特許請求の範囲第1項記載の組成物。
[Claims] 1. One or two selected from the group consisting of sodium dichloroisocyanurate, potassium dichloroisocyanurate, and dichloroisocyanuric acid.
1. A stabilized composition for a powdered chlorine bleach, comprising at least one powdered chlorine bleach and a crystal type A zeolite in a weight ratio of 97/3 to 70/30. 2. The composition according to claim 1, wherein the water content of the A-type zeolite is substantially zero.
JP19971281A 1981-12-11 1981-12-11 Stabilizing composition for powder chlorine bleaching agent Granted JPS58101199A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19971281A JPS58101199A (en) 1981-12-11 1981-12-11 Stabilizing composition for powder chlorine bleaching agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19971281A JPS58101199A (en) 1981-12-11 1981-12-11 Stabilizing composition for powder chlorine bleaching agent

Publications (2)

Publication Number Publication Date
JPS58101199A JPS58101199A (en) 1983-06-16
JPH0335359B2 true JPH0335359B2 (en) 1991-05-27

Family

ID=16412350

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19971281A Granted JPS58101199A (en) 1981-12-11 1981-12-11 Stabilizing composition for powder chlorine bleaching agent

Country Status (1)

Country Link
JP (1) JPS58101199A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4389325A (en) * 1982-01-25 1983-06-21 Monsanto Company Chloroisocyanurate compositions
JPS61145169A (en) * 1984-12-18 1986-07-02 Nissan Chem Ind Ltd Storage of solid chlorination agent
JPS6225198A (en) * 1985-07-25 1987-02-03 ユ−ホ−ケミカル株式会社 Bleaching detergent composition
FR2658194B1 (en) * 1990-02-15 1994-05-20 Norsolor Sa PROCESS FOR STORING CHLOROISOCYANURATES.
JP4708776B2 (en) * 2004-12-10 2011-06-22 エステー株式会社 Solid drain pipe cleaning agent and drain pipe cleaning method

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5197608A (en) * 1975-01-24 1976-08-27

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5197608A (en) * 1975-01-24 1976-08-27

Also Published As

Publication number Publication date
JPS58101199A (en) 1983-06-16

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