JPH02229898A - Bleaching detergent composition - Google Patents

Bleaching detergent composition

Info

Publication number
JPH02229898A
JPH02229898A JP1230776A JP23077689A JPH02229898A JP H02229898 A JPH02229898 A JP H02229898A JP 1230776 A JP1230776 A JP 1230776A JP 23077689 A JP23077689 A JP 23077689A JP H02229898 A JPH02229898 A JP H02229898A
Authority
JP
Japan
Prior art keywords
component
hydrogen peroxide
peroxide
bleaching
weight
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
JP1230776A
Other languages
Japanese (ja)
Inventor
Muneo Aoyanagi
青柳 宗郎
Mutsumi Kuroda
睦 黒田
Hiroyuki Araki
宏幸 荒木
Akio Taguchi
田口 昭男
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 JP1230776A priority Critical patent/JPH02229898A/en
Publication of JPH02229898A publication Critical patent/JPH02229898A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3902Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905Bleach activators or bleach catalysts
    • C11D3/3907Organic compounds
    • C11D3/3917Nitrogen-containing compounds
    • C11D3/3927Quarternary ammonium compounds

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

PURPOSE:To provide the subject composition containing a peroxide, a bleaching activator and a mixture of surfactants such as an alkylbenzenesulfonic acid salt at specific ratios, having high bleaching effect and effective in preventing the redeposition of soiling. CONSTITUTION:The objective composition contains (A) 3-30wt.% of a peroxide capable of forming hydrogen peroxide when dissolved in water, (B) 0.1-30wt.% of a bleaching activator capable of forming an organic peracid having cationic group by reacting with hydrogen peroxide and (C) 10-50wt.% of a surfactant mixture composed of (i) an alkylbenzenesulfonic acid salt, (ii) an alkylsulfuric acid salt and (iii) a polyoxyethylene alkyl ether at weight ratios of the components i, ii and iii falling within the range enclosed by the points (90%, 9%, 1%), (60%, 39%, 1%), (60%, 20%, 20%), (75%, 5%, 20%) and (90%, 5%, 5%) on triangular coordinates.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は特定の漂白活性化剤を含有する漂白洗剤組成物
に関する. 〔従来の技術〕 従来より漂白洗剤には過炭酸ソーダ、過硼酸ソーダなど
の酸素系漂白剤が配合されている。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to bleaching detergent compositions containing specific bleach activators. [Prior Art] Conventionally, bleaching detergents contain oxygen bleaching agents such as sodium percarbonate and sodium perborate.

酸素系漂白剤は塩素系漂白剤にくらべ漂白カが弱《各種
漂白活性化剤が併用されている。代表的な活性化剤とし
て、テトラアセチルエチレンジアミン、アセトキシベン
ゼンスルボン酸ソーダ、イソノナノイルオキシベンゼン
スルボン酸ソーダ、テトラアセチルグリコリルウリル、
グルコースベンタアセテートなどが汎用されている。
Oxygen bleach has weaker bleaching power than chlorine bleach (various bleach activators are used in combination). Typical activators include tetraacetylethylenediamine, sodium acetoxybenzenesulfonate, sodium isononanoyloxybenzenesulfonate, tetraacetylglycolyluril,
Glucose bentaacetate and the like are commonly used.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

本発明者らは、前述した漂白活性化剤より優れた活性化
効果を示す漂白活性化剤について研究した結果、カチオ
ン基を有する活性化剤であり、しかも過酸化水素と反応
してカチオン基を有する有機過酸を生成する活性化剤が
漂白力を著しく向上することを見い出した。衣類あるい
は汚れの多くは負に帯電しているので、これらの漂白活
性化剤が衣類又は汚れの表面上に吸着あるいは濃縮され
た状態で存在し漂白効率を高めているものと推測される
.しかしながら、さらに研究を続けた結果、カチオン基
を有する漂白活性化剤を配合した漂白洗剤は再汚染の問
題を生ずることが判明した. (課題を解決するための手段〕 本発明者らは、漂白洗剤系にカチオン基を有する漂白活
性化剤を併用すべく鋭意研究した結果、特定の界面活性
剤併用系であれば前述の再汚染の問題を解決できること
を見い出し本発明を完成した. 即ち、本発明は、 (a)  水に溶解して過酸化水素を生成する過酸化物
3〜30重量% (b)  過酸化水素と反応してカチオン基を有する有
機過酸を生成する漂白活性化剤0.1〜30重量% (c)  アルキルベンゼンスルホン酸塩(d)  ア
ルキル硫酸塩 (e)  ポリオキシエチレンアルキルエーテル(c)
 + (d) + (e) = 10 〜50重量%(
c). (d), (e)3成分の配合比は添付図面に
示す三角図表の点A(c成分90%、d成分9%、e成
分1%)、B(c成分60%、d成分39%、e成分1
%)、C(c成分60%、d成分20%、e成分20%
)、D(c成分75%、d成分5%、e成分20%)、
ECc成分90%、d成分5%、e成分5%)で囲まれ
た範囲内にある を含有することを特徴とする漂白洗剤組成物を提供する
ものである. 本発明に用いられる(a)成分の水に溶解して過酸化水
素を生成する過酸化物としては脊機及び無機過酸化水素
付加物である炭酸ナトリウム・過酸化水素付加物(過炭
酸ソーダ)、トリポリリン酸ナトリウム・過酸化水素付
加物、ピロリン酸ナ} IJウム・過酸化水素付加物、
尿素・過酸化水素付加物、又は4NatSO4・2Hz
Oz48Cl等が例示される。又、過ホウ酸ナトリウム
ー水化物、過ホウ酸ナトリウム四水化物、過酸化ナトリ
ウム、過酸化カルシウム等の無機過酸化物も使用できる
。この中でも特に炭酸ナトリウム・過酸化水素付加物、
過ホウ酸ナトリウムー水化物、過ホウ酸ナトリウム四水
化物が好ましい.(a)成分の過酸化物は本発明の組成
物中に3〜30重量%、好ましくは5〜15重量%配合
される。
The present inventors researched a bleach activator that has a superior activation effect than the bleach activators mentioned above, and found that it is an activator that has a cationic group, and that it reacts with hydrogen peroxide to generate a cationic group. It has been found that an activator that generates an organic peracid with a compound of the present invention significantly improves bleaching power. Since most clothing and stains are negatively charged, it is assumed that these bleach activators exist in an adsorbed or concentrated state on the surface of clothing or stains, increasing bleaching efficiency. However, further research revealed that bleach detergents containing bleach activators with cationic groups cause recontamination problems. (Means for Solving the Problems) As a result of intensive research into the use of a bleach activator having a cationic group in a bleach detergent system, the present inventors found that if a system in combination with a specific surfactant is used, the above-mentioned re-contamination can be avoided. The present invention was completed after discovering that the following problems could be solved.That is, the present invention consists of: (a) 3 to 30% by weight of peroxide that dissolves in water to produce hydrogen peroxide; (b) Reacts with hydrogen peroxide. 0.1 to 30% by weight of a bleach activator that produces an organic peracid having a cationic group (c) Alkylbenzene sulfonate (d) Alkyl sulfate (e) Polyoxyethylene alkyl ether (c)
+ (d) + (e) = 10 to 50% by weight (
c). (d), (e) The blending ratios of the three components are points A (90% c component, 9% d component, 1% e component) and B (60% c component, 39% d component) on the triangular diagram shown in the attached drawing. , e component 1
%), C (c component 60%, d component 20%, e component 20%
), D (c component 75%, d component 5%, e component 20%),
The present invention provides a bleaching detergent composition characterized in that it contains 90% of an ECc component, 5% of a d component, and 5% of an e component. Component (a) used in the present invention, a peroxide that dissolves in water to produce hydrogen peroxide, is a sodium carbonate/hydrogen peroxide adduct (soda percarbonate), which is a spinal and inorganic hydrogen peroxide adduct. , sodium tripolyphosphate/hydrogen peroxide adduct, sodium pyrophosphate} IJium/hydrogen peroxide adduct,
Urea/hydrogen peroxide adduct or 4NatSO4/2Hz
Examples include Oz48Cl. Inorganic peroxides such as sodium perborate hydrate, sodium perborate tetrahydrate, sodium peroxide, and calcium peroxide can also be used. Among these, especially sodium carbonate/hydrogen peroxide adducts,
Sodium perborate hydrate and sodium perborate tetrahydrate are preferred. Component (a), peroxide, is blended in the composition of the present invention in an amount of 3 to 30% by weight, preferably 5 to 15% by weight.

本発明に用いられる(b)成分の過酸化水素と反応して
カチオン基を有する有機過酸を生成する漂白活性化剤と
しては、例えば、次のような化合物が挙げられる。
Examples of the bleach activator used in the present invention that reacts with hydrogen peroxide, component (b), to produce an organic peracid having a cationic group include the following compounds.

Rz ?l−(A)T(B) l,−N工(c11■)l−(
0),−C−L  X−   (1)R3      
    0 式(1)中、R+はCl−Il+、特に01〜,4の直
鎖又は分岐のアルキル基、Aは一〇 −  −NHC 
−  −CNH!1 C!1, I Bは−{CHzh ,40CHzCHt}−又は−{O
CRCHアh(mは1〜12、特に1〜5が好ましく、
nは1〜10、特に1〜5が好ましい。)である,a.
bはa=O,b−0であるか、又はa=1,b=1であ
るa Rz+ ”は炭素数1〜3のアルキル基又はヒド
ロキシアルキル基である。lは1〜l2であり、CはO
又は1である。Lは脱M基であり、下記の(イ)〜(夕
)から選ばれる。
Rz? l-(A)T(B) l,-N Engineering (c11 ■) l-(
0), -C-L X- (1) R3
0 In formula (1), R+ is Cl-Il+, especially a linear or branched alkyl group of 01 to 4, and A is 10--NHC
- -CNH! 1 C! 1, IB is -{CHzh,40CHzCHt}- or -{O
CRCHah (m is preferably 1 to 12, particularly preferably 1 to 5,
n is preferably 1 to 10, particularly preferably 1 to 5. ), a.
b is a=O, b-0, or a=1, b=1 a Rz+ '' is an alkyl group or hydroxyalkyl group having 1 to 3 carbon atoms; 1 is 1 to 12; C is O
Or 1. L is a de-M group and is selected from the following (a) to (y).

ル4、RllはC3〜C4のアルキレン基、R,はフェ
ニル基又はC1。〜C3。のアルキル基、YはI1又は
R2 リ金属を表す。) 一般式(1)においてX−は無機又は有機の対イ(力)
−0−R..(ヨ)グリセリン残基,又は (タ)糖誘導体残基 (式中、R4はC,〜C2のアルキル基、Rs.Rhは
H又はC,−Ctのアルキル基、R7はC I− C 
tのアルキR1。:炭素数1〜20のアルキル基 RII+RI+!’炭素数1〜3のアルキル基又はヒド
ロキシアルキル基 l:1〜20 Y : H, COzO,S(hO,COtM又はSO
J (MはH又はアルカリ金属) ? :アニオン(但し、YがCO■e,S■,(E)の
時番よXはない.) R目 ■ Rho  N  GHz  CN X0 (III) Lx R+a+ Rll+ Rlt+ X ’上記と同じR目 R+o+ RII+ Rtz+ X ’上記と同じm:
1〜3 Rz+ R+t+ X :前記と同じ R+3rRI4;炭素数1〜3のアルキル基又はヒドロ
キシアルキル基 n :1〜16 X,Yは上記と同じ 本発明における(b)成分は、これらの例に示されるよ
うに過酸化水素と反応してカチオン基を有する有機過酸
を生成する構造を有していればよく、これらの化合物に
限定されるものではない。(b)成分の漂白活性化剤は
組成物中に0.1〜30重量%、好ましくは2〜15重
量%配合される。
R4, Rll is a C3-C4 alkylene group, and R is a phenyl group or C1. ~C3. an alkyl group, Y represents I1 or R2 metal. ) In general formula (1), X- is an inorganic or organic pair (force)
-0-R. .. (y) Glycerin residue or (t) sugar derivative residue (in the formula, R4 is a C, -C2 alkyl group, Rs.Rh is a H or C, -Ct alkyl group, R7 is a C I- C
alkyl R1 of t. : C1-C20 alkyl group RII+RI+! 'Alkyl group or hydroxyalkyl group having 1 to 3 carbon atoms l: 1 to 20 Y: H, COzO, S (hO, COtM or SO
J (M is H or alkali metal)? : Anion (However, when Y is CO■e, S■, (E), there is no X.) Rth ■ Rho N GHz CN X0 (III) Lx R+a+ Rll+ Rlt+ X 'Same Rth as above R+o+ RII+ Rtz+X'm same as above:
1-3 Rz+ R+t+ X: Same as above R+3rRI4; C1-3 alkyl group or hydroxyalkyl group n: 1-16 The compound is not limited to these compounds as long as it has a structure that reacts with hydrogen peroxide to produce an organic peracid having a cationic group, as shown in FIG. Component (b), a bleach activator, is incorporated in the composition in an amount of 0.1 to 30% by weight, preferably 2 to 15% by weight.

本発明に用いられる(c)成分のアルキルベンゼンスル
ホン酸塩としては、平均炭素数10〜l6のアルキル基
を有する直鎖又は分岐鎖アルキルベンゼンスルホン酸塩
が挙げられ、(d)成分のアルキル硫酸塩としては平均
炭素数10〜20のアルキル基を有するアルキル硫酸塩
が挙げられる。(c),(d)成分の対イオンとしては
ナトリウム、カリウム等のアルカリ金属イオンが挙げら
れる。(e)成分のポリオキンエチレンアルキルエーテ
ルとしては平均炭素数10〜20のアルキル基を存し、
1〜30モルのエチレンオキサイドを付加したポリオキ
シエチレンアルキルエーテルが挙げられる.本発明の組
成物中の(c), (d). (e)成分は前述した配
合比範囲になければならない。この範囲外ではカチオン
性の有機過酸を生成する漂白活性化剤を使用した場合再
汚染防止効果が不十分である. (c). (d), 
(e)成分の配合比の好ましい範囲は、F(c成分85
%、d成分13%、e成分2%)、G (c成分65%
、d成分33%、e成分2%)、H(c成分65%、d
成分20%、e成分15%)、I(c成分75%、d成
分10%、e成分15%) 、J (c成分85%、d
成分10%、e成分5%)で囲まれた範囲である. (
c). (d). (e)成分は本発明の組成物中に総
量で10〜50重量%、好ましくは15〜40重量%配
合される. 本発明の組成物には次の様な漂白洗剤常用成分を必要に
応じて配合し得る。
Examples of the alkylbenzene sulfonate as the component (c) used in the present invention include linear or branched alkylbenzene sulfonates having an alkyl group having an average carbon number of 10 to 16; Examples include alkyl sulfates having an alkyl group having an average carbon number of 10 to 20. Counter ions for components (c) and (d) include alkali metal ions such as sodium and potassium. (e) The polyoxine ethylene alkyl ether has an alkyl group having an average carbon number of 10 to 20,
Examples include polyoxyethylene alkyl ethers to which 1 to 30 moles of ethylene oxide are added. (c), (d) in the composition of the invention. Component (e) must be in the above-mentioned mixing ratio range. Outside this range, if a bleach activator that generates a cationic organic peracid is used, the recontamination prevention effect will be insufficient. (c). (d),
The preferred range of the blending ratio of component (e) is F (component c: 85
%, d component 13%, e component 2%), G (c component 65%
, d component 33%, e component 2%), H (c component 65%, d
component 20%, e component 15%), I (c component 75%, d component 10%, e component 15%), J (c component 85%, d
component (10%, e component 5%). (
c). (d). Component (e) is incorporated in the composition of the present invention in a total amount of 10 to 50% by weight, preferably 15 to 40% by weight. If necessary, the composition of the present invention may contain the following commonly used bleaching detergent ingredients.

即ち、ケイ酸塩、炭酸塩、セスキ炭酸塩、硫酸塩、オル
トリン酸塩、ピロリン酸塩、トリポIJ IJン酸塩、
クエン酸塩、イソクエン酸塩、エチレンジアミン四酢酸
塩、ニトリロトリ酢酸塩、ポリアセタールカルボン酸塩
、ゼオライトなどのビルダー類が普通40〜75重量%
配合される。
i.e. silicates, carbonates, sesquicarbonates, sulfates, orthophosphates, pyrophosphates, trypoIJIJ phosphates,
Usually 40-75% by weight of builders such as citrate, isocitrate, ethylenediaminetetraacetate, nitrilotriacetate, polyacetal carboxylate, zeolite etc.
It is blended.

又、他のア二オン界面活性剤、ノニオン界面活性剤、両
性界面活性剤なども適宜配合し得る。
In addition, other anionic surfactants, nonionic surfactants, amphoteric surfactants, etc. may also be blended as appropriate.

その他ポリビニルアルコール、ポリビニルピロリドン、
カルボキシメチルセルロース、ボリエチレングリコール
、ポリアクリル酸塩などの再汚染防止剤、プロテアーゼ
、エスペラーゼ、リパーゼ、セルラーゼなどの酵素、そ
の他ケーキング防止剤、酸化防止剤、螢光染料、青味付
剤、光活性化漂白剤、香料なども配合される.〔実施例
〕 以下実施例に基づいて本発明を説明するが、本発明はこ
れら実施例に限定されるものではない.尚、実施例にお
いて、漂白率及び再汚染防止能の試験は以下に示す方法
によって行った.く漂白率の試験法〉 洗剤濃度0.083%の洗浄液に下記方法で調製した紅
茶汚染布(8X8cd、5枚)を入れターゴトメーター
で20”C,10分洗浄した後、水洗い、乾燥後、下記
方法により漂白率を求めた。
Others polyvinyl alcohol, polyvinylpyrrolidone,
Recontamination inhibitors such as carboxymethyl cellulose, polyethylene glycol, and polyacrylates, enzymes such as protease, esperase, lipase, and cellulase, other caking inhibitors, antioxidants, fluorescent dyes, blue tinting agents, and photoactivation. Bleach and fragrance are also included. [Examples] The present invention will be described below based on Examples, but the present invention is not limited to these Examples. In the Examples, the bleaching rate and recontamination prevention ability were tested by the methods shown below. Test method for bleaching rate> Put black tea-stained cloth (8 x 8 cd, 5 sheets) prepared in the following method into a cleaning solution with a detergent concentration of 0.083%, wash with a tergotometer at 20"C for 10 minutes, then wash with water and dry. The bleaching rate was determined by the following method.

紅茶汚染布: 日東紅茶(黄色パッケージ)80gを32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
、この液に木綿金巾#2003布を浸し、約15分間煮
沸する。そのまま火よりおろし、2時間程度放置後自然
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、8C11X8C11の試験片とし、実験に供
した.紅茶汚染布の漂白率: 反射率は日本電色工業■製NOR−101DPで460
nmフィルターを使用して測定した。
Tea-contaminated cloth: Boil 80 g of Nitto black tea (yellow package) in 32 ion exchange water for about 15 minutes, strain it through desized dry cotton cloth, soak a #2003 cotton cloth in the liquid, and boil it for about 15 minutes. Remove from the heat, let stand for about 2 hours, then dry naturally. Rinse with water until the washing liquid is no longer colored, dehydrate,
After pressing, it was made into an 8C11 x 8C11 test piece and used for experiments. Bleaching rate of black tea contaminated cloth: Reflectance is 460 for NOR-101DP manufactured by Nippon Denshoku Kogyo ■
Measured using a nm filter.

〈再汚染防止能の試験法〉 (1)試験布 木綿(2003布)を10 X IOCI1に裁断し試
験布とする。
<Test method for anti-recontamination ability> (1) Test cloth Cut cotton (2003 cloth) into 10 x IOCI1 pieces to use as a test cloth.

(2)汚れ 疎水性固体汚れ:カーボンブラック.平均粒径0.1μ 親水性固体汚れ;鹿沼赤玉土,200メッシュのフルイ
にかけた通過品 (3)実験条件 温度;20℃ 硬度;4“DI 洗剤濃度; 0.083% 汚れ;カーボン 0.25g/It 泥     2.5g//! ターゴトメーター10Or. p.mで10分汚染、流
水すすぎ (4)実験方法 12のビーカーに、カーボン及び泥を指定量、サンプリ
ングし、指定濃度に溶かした洗剤液を少しずつ入れ、ガ
ラス棒で分散させ、温度を趨整し、ターゴトメーターの
試料カップに入れ、試験布3枚を投入し、100r.p
.mで10分間汚染させ、流水ですすぎ、プレス乾燥し
、日本電色工業■製NDR−101DPにて再汚染防止
率を求めた. R(0)・・・原布の反射率 R (S)・・・汚染後の反射率 実施例1 下記配合組成を有する漂白洗剤を製造し、漂白率及び再
汚染防止率を求めた.結果を表−1に示す. 〈洗剤配合組成〉 ボリエチレングリコール(MW13QOO)プロテアー
ゼ 水 アルキル硫酸ソーダCCla〜1,)表−1に示す量2
号珪酸ソーダ 炭酸ソーダ 4A型ゼオライト 硫酸ソーダ 過炭酸ソーダ 実施例2 下記配合組成を有する漂白洗剤を製造し、漂白率及び再
汚染防止率を求めた。結果を表−2に示す。
(2) Soil Hydrophobic solid stain: carbon black. Average particle size: 0.1μ Hydrophilic solid stain; Kanuma Akadama clay, passed through a 200 mesh sieve (3) Experimental conditions Temperature: 20°C Hardness: 4"DI Detergent concentration: 0.083% Soil; Carbon 0.25g /It Mud 2.5g//! Contaminate with Tergotometer 10 Or. p.m for 10 minutes, rinse with running water (4) In the beaker of Experimental Method 12, sample the specified amount of carbon and mud, and dissolve the detergent to the specified concentration. Pour the liquid little by little, disperse it with a glass rod, adjust the temperature, put it in the sample cup of the tergotometer, add 3 test cloths, and set it at 100 rpm.
.. The sample was contaminated with water for 10 minutes, rinsed with running water, press dried, and the recontamination prevention rate was determined using NDR-101DP manufactured by Nippon Denshoku Kogyo ■. R(0)...Reflectance of original fabric R(S)...Reflectance after staining Example 1 A bleaching detergent having the following composition was manufactured, and the bleaching rate and re-staining prevention rate were determined. The results are shown in Table 1. <Detergent composition> Polyethylene glycol (MW13QOO) Protease water alkyl sulfate sodium CCla~1,) Amount shown in Table 1 2
Sodium silicate soda Sodium carbonate Type 4A zeolite Sodium sulfate Sodium percarbonate Example 2 A bleaching detergent having the following composition was produced, and the bleaching rate and re-staining prevention rate were determined. The results are shown in Table-2.

〈洗剤配合組成〉 アルキル硫酸ソーダ(c+z〜1,)8牛脂脂肪酸ソー
ダ 2号珪酸ソーダ 炭酸ソーダ 4A型ゼオライト 硫酸ソーダ 過炭酸ソーダ 漂白活性化剤(表−2) ポリエチレングリコール(?IW6000)プロテアー
ゼ 水 4.
<Detergent composition> Sodium alkyl sulfate (c+z~1,) 8 Beef tallow fatty acid soda No. 2 Sodium silicate Sodium carbonate 4 A type zeolite Sodium sulfate Sodium percarbonate Bleach activator (Table 2) Polyethylene glycol (?IW6000) Protease water 4 ..

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の(c)、 (d)、 (e)3成分の配合比 を示す三角図である。 FIG. 1 shows (c) of the present invention. (d), (e) Mixing ratio of three components FIG.

Claims (1)

【特許請求の範囲】 1、(a)水に溶解して過酸化水素を生成する過酸化物
3〜30重量% (b)過酸化水素と反応してカチオン基を有する有機過
酸を生成する漂白活性化剤0.1〜30重量% (c)アルキルベンゼンスルホン酸塩 (d)アルキル硫酸塩 (e)ポリオキシエチレンアルキルエーテル(c)+(
d)+(e)=10〜50重量%(c)、(d)、(e
)3成分の配合比は添付図面に示す三角図表の点A(c
成分90%、d成分9%、e成分1%)、B(c成分6
0%、d成分39%、e成分1%)、C(c成分60%
、d成分20%、e成分20%)、D(c成分75%、
d成分5%、e成分20%)、E(c成分90%、d成
分5%、e成分5%)で囲まれた範囲 内にある を含有することを特徴とする漂白洗剤組成物。
[Claims] 1. (a) 3 to 30% by weight of peroxide that dissolves in water to produce hydrogen peroxide (b) Reacts with hydrogen peroxide to produce an organic peracid having a cationic group. Bleach activator 0.1-30% by weight (c) Alkylbenzene sulfonate (d) Alkyl sulfate (e) Polyoxyethylene alkyl ether (c) + (
d) + (e) = 10-50% by weight (c), (d), (e
) The blending ratio of the three components is determined by point A (c) on the triangular diagram shown in the attached drawing.
component 90%, d component 9%, e component 1%), B (c component 6
0%, d component 39%, e component 1%), C (c component 60%
, d component 20%, e component 20%), D (c component 75%,
A bleaching detergent composition, characterized in that it contains within the range of (5% component d, 20% component e) and E (90% component c, 5% component d, 5% component e).
JP1230776A 1988-09-22 1989-09-06 Bleaching detergent composition Pending JPH02229898A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1230776A JPH02229898A (en) 1988-09-22 1989-09-06 Bleaching detergent composition

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP63-237929 1988-09-22
JP23792988 1988-09-22
JP1230776A JPH02229898A (en) 1988-09-22 1989-09-06 Bleaching detergent composition

Publications (1)

Publication Number Publication Date
JPH02229898A true JPH02229898A (en) 1990-09-12

Family

ID=26529531

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1230776A Pending JPH02229898A (en) 1988-09-22 1989-09-06 Bleaching detergent composition

Country Status (1)

Country Link
JP (1) JPH02229898A (en)

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