JPH04337399A - Liquid bleaching agent composition - Google Patents

Liquid bleaching agent composition

Info

Publication number
JPH04337399A
JPH04337399A JP11027391A JP11027391A JPH04337399A JP H04337399 A JPH04337399 A JP H04337399A JP 11027391 A JP11027391 A JP 11027391A JP 11027391 A JP11027391 A JP 11027391A JP H04337399 A JPH04337399 A JP H04337399A
Authority
JP
Japan
Prior art keywords
bleach
hydrogen peroxide
agent composition
liquid
composition
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.)
Pending
Application number
JP11027391A
Other languages
Japanese (ja)
Inventor
Tatsunori Tamura
辰仙 田村
Muneo Aoyanagi
青柳 宗郎
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 JP11027391A priority Critical patent/JPH04337399A/en
Priority to US08/433,408 priority patent/US5827447A/en
Publication of JPH04337399A publication Critical patent/JPH04337399A/en
Pending legal-status Critical Current

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  • Detergent Compositions (AREA)
  • Treatment Of Fiber Materials (AREA)

Abstract

PURPOSE:To obtain a liquid bleaching agent composition, having transparent appearance and excellent in preservation stability and bleaching power. CONSTITUTION:A transparent liquid bleaching agent composition containing (a) hydrogen peroxide, (b) an anionic surfactant and (c) an amphoteric bleaching activator, reactive with the hydrogen peroxide and producing an organic peracid having a quaternary ammonium group in a specific proportion.

Description

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

【0001】0001

【産業上の利用分野】本発明は液体漂白剤組成物に関し
、更に詳しくは貯蔵安定性に優れ、しかも漂白力の良好
な液体漂白剤組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a liquid bleach composition, and more particularly to a liquid bleach composition having excellent storage stability and good bleaching power.

【0002】0002

【従来の技術】漂白剤には化学的に分類すると塩素系漂
白剤と酸素系漂白剤とに分けられる。また、物理的に分
類すると固体状(粉末)と液体状とに分けられる。
Bleaching agents are chemically classified into chlorine bleaching agents and oxygen bleaching agents. Moreover, when classified physically, it can be divided into solid (powder) and liquid.

【0003】塩素系漂白剤は使用できる繊維に制限があ
り、又色、柄物には使用できず、更に独自のにおいを有
していることなどから、これらの欠点のない酸素系漂白
剤が最近著しく普及しはじめている。
[0003] Chlorine bleach has limitations on the types of fibers that can be used, cannot be used on colored or patterned fabrics, and has a unique odor. It is starting to spread significantly.

【0004】この酸素系漂白剤のうち、固体状のものは
過炭酸ナトリウム、過硼酸ナトリウムが漂白性能及び安
定性などの面から特に利用されており、過酸化水素を使
用した液体状の漂白剤もその簡便性によりかなり普及し
てきている。
[0004] Among these oxygen bleaches, solid ones such as sodium percarbonate and sodium perborate are particularly used from the viewpoint of bleaching performance and stability, and liquid bleaches using hydrogen peroxide are used. It has become quite popular due to its simplicity.

【0005】酸素系漂白剤は塩素系漂白剤にくらべ漂白
力が弱く、各種漂白活性化剤が併用されている。この漂
白活性化剤にはアセトニトリル等に代表されるニトリル
類、グルコースペンタアセテート(GPAC)等に代表
される O−アセチル化物、テトラアセチルエチレンジ
アミン(TAED)等に代表される N−アシル化物、
無水マレイン酸等に代表される酸無水物等が挙げられる
[0005] Oxygen bleaches have weaker bleaching power than chlorine bleaches, and various bleach activators are used in combination. These bleach activators include nitriles such as acetonitrile, O-acetylated products such as glucose pentaacetate (GPAC), N-acylated products such as tetraacetylethylenediamine (TAED), etc.
Examples include acid anhydrides represented by maleic anhydride.

【0006】また、本発明者らの研究の結果、特開昭6
3−233969号公報、特開昭63−315666号
公報、特開昭64−68347 号公報、特開平1−1
90654号公報等に例示されるような過酸化水素と反
応して第4級アンモニウム基を有する有機過酸を生成す
る化合物が漂白活性化剤として極めて優れていることが
見出されている。
[0006] Furthermore, as a result of research by the present inventors,
3-233969, JP 63-315666, JP 64-68347, JP 1-1
It has been found that compounds that react with hydrogen peroxide to produce organic peracids having a quaternary ammonium group, such as those exemplified in Japanese Patent No. 90654, are extremely effective as bleach activators.

【0007】固体状の組成物の場合には固体状過酸塩と
これらと有機過酸を生成する乾燥粒子としての固体状活
性化剤とを混合することにより、貯蔵安定性が得られる
。これらが貯蔵中に乾燥状態に保たれる限り混合物を洗
濯機等の水中へ投入するまで著しい反応又は活性損失が
起こらない。例えば、浴室内におけるような高湿度環境
においては乾燥漂白剤が湿って活性が低下する。液体過
酸化水素が過酸化物源として用いられるときには乾燥粒
子状漂白剤を得ることは不可能である。
In the case of solid compositions, storage stability is achieved by mixing solid persalts with solid activators as dry particles which form organic peracids. As long as they are kept dry during storage, no significant reaction or activity loss occurs until the mixture is placed in water, such as in a washing machine. For example, in a high humidity environment, such as in a bathroom, dry bleach becomes damp and becomes less active. It is not possible to obtain dry particulate bleach when liquid hydrogen peroxide is used as the peroxide source.

【0008】これまで、液体過酸化水素漂白剤組成物に
ついていくつかの提案がなされてきた。このうち、有機
過酸を生成する漂白活性化剤を利用したものとして特開
昭62−230897号公報には過酸化水素酸性水溶液
中に固体状の漂白活性化剤を分散させた貯蔵安定・低温
活性の組成物が開示されている。しかしこの組成物は透
明ではなく、漂白活性化剤が分散している状態であり、
貯蔵中に漂白活性化剤が沈澱分離してくる。有機過酸を
生成する漂白活性化剤を溶解させた液体漂白剤組成物は
ない。
[0008] Several proposals have been made for liquid hydrogen peroxide bleach compositions. Among these, JP-A No. 62-230897 discloses a method using a bleach activator that generates organic peracid, which is a storage-stable, low-temperature solution in which a solid bleach activator is dispersed in an acidic aqueous solution of hydrogen peroxide. Active compositions are disclosed. However, this composition is not transparent and contains a bleach activator dispersed in it.
During storage, the bleach activator precipitates and separates. There are no liquid bleach compositions with dissolved bleach activators that produce organic peracids.

【0009】[0009]

【発明が解決しようとする課題】従って、漂白活性化剤
を溶解させて透明とし、貯蔵安定性が改善され、より高
漂白力の液体酸素系漂白剤が要求されており、本発明の
目的はそのような液体酸素系漂白剤組成物を提供するこ
とにある。
[Problems to be Solved by the Invention] Therefore, there is a need for a liquid oxygen bleaching agent that dissolves the bleach activator to make it transparent, has improved storage stability, and has higher bleaching power. An object of the present invention is to provide such a liquid oxygen bleach composition.

【0010】0010

【課題を解決するための手段】本発明者らは貯蔵安定性
に優れた透明な液体酸素系漂白剤組成物で、より高漂白
力を有するものを得るべく鋭意研究の結果、アニオン性
界面活性剤と第4級アンモニウム基を有する有機過酸を
生成する両性の漂白活性化剤とを組み合わせることによ
り、漂白活性化剤を均一透明に溶解することができ、し
かも過酸化水素中でも非常に安定化し透明な液体酸素系
漂白剤組成物が得られることを見出し、本発明を完成す
るに至った。
[Means for Solving the Problems] The present inventors have conducted intensive research to obtain a transparent liquid oxygen bleach composition with excellent storage stability and higher bleaching power. By combining the bleach activator with an amphoteric bleach activator that generates an organic peracid having a quaternary ammonium group, the bleach activator can be dissolved uniformly and transparently, and is extremely stable even in hydrogen peroxide. It was discovered that a transparent liquid oxygen bleach composition could be obtained, and the present invention was completed.

【0011】すなわち本発明は、 (a) 過酸化水素                
                         
  0.5〜10重量%(b) アニオン性界面活性剤 (c) 過酸化水素と反応して第4級アンモニウム基を
有する有機過酸を生成する両性の漂白活性化剤を (b
)+(c) = 0.1〜50重量%、 (b)/(c
) =50/1〜1/3(重量比)の範囲で含有してな
る透明な液体漂白剤組成物を提供するものである。
[0011] That is, the present invention provides: (a) hydrogen peroxide;

0.5-10% by weight (b) Anionic surfactant (c) An amphoteric bleach activator that reacts with hydrogen peroxide to produce an organic peracid having a quaternary ammonium group (b)
)+(c) = 0.1-50% by weight, (b)/(c
)=50/1 to 1/3 (weight ratio).

【0012】本発明に用いられるアニオン性界面活性剤
(b) としては、例えば、直鎖又は分岐鎖アルキル 
(C8〜C18)ベンゼンスルホン酸塩、アルキル又は
アルケニル (C8〜C18)エーテル硫酸塩、アルキ
ル又はアルケニル (C8〜C18)硫酸塩、オレフィ
ン(C12〜C18)スルホン酸塩、アルカンスルホン
酸塩、飽和又は不飽和脂肪酸塩等が挙げられる。
The anionic surfactant (b) used in the present invention includes, for example, straight-chain or branched-chain alkyl
(C8-C18) Benzene sulfonate, alkyl or alkenyl (C8-C18) Ether sulfate, alkyl or alkenyl (C8-C18) sulfate, olefin (C12-C18) sulfonate, alkanesulfonate, saturated or Examples include unsaturated fatty acid salts.

【0013】本発明に用いられる過酸化水素と反応して
第4級アンモニウム基を有する有機過酸を生成する両性
の漂白活性化剤(c) としては、例えば次の構造を有
するものが挙げられる。
[0013] Examples of the amphoteric bleach activator (c) that reacts with hydrogen peroxide to produce an organic peracid having a quaternary ammonium group used in the present invention include those having the following structure. .

【0014】[0014]

【化1】[Chemical formula 1]

【0015】a,b はa =0,b =0であるか、
又はa =1,b =1である。R2,R3はC1〜C
2のアルキル基である。
[0015] Are a and b a = 0, b = 0?
Or a = 1, b = 1. R2 and R3 are C1 to C
2 is an alkyl group.

【0016】連結基は特に限定されるものではないが、
例えば直鎖又は分岐鎖のアルキレン基、シクロアルキレ
ン基、フェニレン基又はアルキレンフェニレン基、オキ
シアルキレン基 (−CH2CH2O−) 、−CpH
2p−(p は1〜12、好ましくは1〜5である)等
である。また、Z は−SO3− 基, −COO− 
基を表す。
[0016] The linking group is not particularly limited, but
For example, linear or branched alkylene group, cycloalkylene group, phenylene group or alkylenephenylene group, oxyalkylene group (-CH2CH2O-), -CpH
2p- (p is 1 to 12, preferably 1 to 5), and the like. Moreover, Z is -SO3- group, -COO-
represents a group.

【0017】これらの漂白活性化剤のうちでも特に望ま
しいのは次の各式で表されるものである。
Among these bleach activators, those represented by the following formulas are particularly desirable.

【0018】[0018]

【化2】[Case 2]

【0019】上記アニオン性界面活性剤(b) 及び過
酸化水素と反応して第4級アンモニウム基を有する有機
過酸を生成する両性の漂白活性化剤(c)は組成物中に
 (b)+(c)総量で 0.1〜50重量%、好まし
くは6〜30重量%配合される。また、(b) 成分と
(c) 成分の重量比は (b)/(c) で50/1
〜1/3、好ましくは10/1〜1/1である。
The above anionic surfactant (b) and an amphoteric bleach activator (c) which reacts with hydrogen peroxide to form an organic peracid having a quaternary ammonium group are present in the composition (b) +(c) The total amount is 0.1 to 50% by weight, preferably 6 to 30% by weight. Also, the weight ratio of component (b) and component (c) is (b)/(c), which is 50/1.
~1/3, preferably 10/1 ~ 1/1.

【0020】本発明の組成物は通常上記(a) 〜(c
) 成分に水を加えてバランスをとり、組成物のpHを
弱酸性ないし酸性(pH6以下、好ましくは 3.5以
下)とするのが望ましい。その他に、増粘剤、香料、色
素、蛍光染料、酵素等を必要に応じ配合してもよい。
[0020] The composition of the present invention usually comprises the above (a) to (c).
) It is desirable to balance the ingredients by adding water to make the pH of the composition weakly acidic to acidic (pH 6 or less, preferably 3.5 or less). In addition, thickeners, fragrances, pigments, fluorescent dyes, enzymes, etc. may be added as necessary.

【0021】[0021]

【実施例】以下実施例にて本発明を説明するが、本発明
はこれらの実施例に限定されるものではない。
[Examples] The present invention will be explained below with reference to Examples, but the present invention is not limited to these Examples.

【0022】実施例1 下記に示す漂白活性化剤を用いて表1に示す各種液体漂
白剤組成物を調製し、それぞれの保存安定性及び漂白効
果を調べた。尚、各組成物のpHは塩酸で3に調整した
。 その結果を表1に示す。
Example 1 Various liquid bleach compositions shown in Table 1 were prepared using the bleach activators shown below, and the storage stability and bleaching effects of each were examined. The pH of each composition was adjusted to 3 with hydrochloric acid. The results are shown in Table 1.

【0023】[0023]

【化3】[Chemical formula 3]

【0024】■保存安定性の評価方法 試料を室温で保存し、保存前後の試料から生成する有機
過酸量を測定し、次式により有効過酸量残存率を算出し
、7日後、80%以上の残存率を示すものを○、80%
未満のものを×とした。
[0024] Storage stability evaluation method: Store the sample at room temperature, measure the amount of organic peracid generated from the sample before and after storage, calculate the effective peracid amount residual rate using the following formula, and after 7 days, it will be 80%. ○ indicates a survival rate of 80% or higher
Those below were marked as ×.

【0025】[0025]

【数1】[Math 1]

【0026】■漂白効果の評価方法 0.8 %の市販洗剤液(pH=10.5)2リットル
に、表1に示す組成の漂白剤組成物を20ccを添加し
、調製した溶液300 mlに紅茶汚染布* を5枚ず
つ20℃, 30分漬け置いた後、水道水ですすぎ、乾
燥させ次式によって漂白率を算出した。尚、反射率は日
本電色性の測色色差計 N−DR 101−DPを用い
て測定した。
■ Method for evaluating bleaching effect 20 cc of the bleach composition shown in Table 1 was added to 2 liters of 0.8% commercially available detergent solution (pH=10.5), and 300 ml of the prepared solution was added. Five black tea contaminated cloths* were soaked at 20°C for 30 minutes, rinsed with tap water, dried, and the bleaching rate was calculated using the following formula. Note that the reflectance was measured using a colorimeter N-DR 101-DP manufactured by Nippon Denchroki.

【0027】[0027]

【数2】[Math 2]

【0028】*紅茶汚染布 日東紅茶(黄色パッケージ)80gを3リットルのイオ
ン交換水にて約15分間煮沸後、糊抜きしたサラシ木綿
でこし、この液に木綿金布#2003布を浸し、約15
分間煮沸する。そのまま火よりおろし、2時間程放置後
、自然乾燥させ、洗液に色のつかなくなるまで水洗し、
脱水、プレス後、8×8cmの試験片とし、実験に供し
た。
*Black tea contaminated cloth After boiling 80 g of Nitto black tea (yellow package) in 3 liters of ion-exchanged water for about 15 minutes, strain it through a desiccated dry cotton cloth, soak a cotton gold cloth #2003 in this liquid, and boil it for about 15 minutes. 15
Boil for minutes. Remove from the heat, leave for about 2 hours, let dry naturally, and wash with water until the washing liquid is no longer colored.
After dehydration and pressing, a test piece of 8 x 8 cm was prepared and used for experiments.

【0029】[0029]

【表1】[Table 1]

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 (a) 過酸化水素                
                         
  0.5〜10重量%(b) アニオン性界面活性剤 (c) 過酸化水素と反応して第4級アンモニウム基を
有する有機過酸を生成する両性の漂白活性化剤を (b
)+(c) = 0.1〜50重量%、 (b)/(c
) =50/1〜1/3(重量比)の範囲で含有してな
る透明な液体漂白剤組成物。
[Claim 1] (a) Hydrogen peroxide

0.5-10% by weight (b) Anionic surfactant (c) An amphoteric bleach activator that reacts with hydrogen peroxide to produce an organic peracid having a quaternary ammonium group (b)
)+(c) = 0.1-50% by weight, (b)/(c
)=50/1 to 1/3 (weight ratio) of a transparent liquid bleach composition.
【請求項2】  組成物のpHが6以下である請求項1
記載の液体漂白剤組成物。
[Claim 2]Claim 1, wherein the pH of the composition is 6 or less.
A liquid bleach composition as described.
JP11027391A 1991-05-15 1991-05-15 Liquid bleaching agent composition Pending JPH04337399A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP11027391A JPH04337399A (en) 1991-05-15 1991-05-15 Liquid bleaching agent composition
US08/433,408 US5827447A (en) 1991-05-15 1992-11-18 Liquid bleaching agent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11027391A JPH04337399A (en) 1991-05-15 1991-05-15 Liquid bleaching agent composition

Publications (1)

Publication Number Publication Date
JPH04337399A true JPH04337399A (en) 1992-11-25

Family

ID=14531508

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11027391A Pending JPH04337399A (en) 1991-05-15 1991-05-15 Liquid bleaching agent composition

Country Status (1)

Country Link
JP (1) JPH04337399A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0670364A4 (en) * 1992-11-18 1996-07-03 Kao Corp Liquid bleach composition.
JP2003089799A (en) * 2001-09-18 2003-03-28 Kao Corp Liquid bleach composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0670364A4 (en) * 1992-11-18 1996-07-03 Kao Corp Liquid bleach composition.
JP2003089799A (en) * 2001-09-18 2003-03-28 Kao Corp Liquid bleach composition

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