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JPH02212599A - liquid cleaning bleach composition - Google Patents

liquid cleaning bleach composition

Info

Publication number
JPH02212599A
JPH02212599A JP1032080A JP3208089A JPH02212599A JP H02212599 A JPH02212599 A JP H02212599A JP 1032080 A JP1032080 A JP 1032080A JP 3208089 A JP3208089 A JP 3208089A JP H02212599 A JPH02212599 A JP H02212599A
Authority
JP
Japan
Prior art keywords
weight
alkali metal
carbon atoms
alkyl
formula
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
Application number
JP1032080A
Other languages
Japanese (ja)
Other versions
JP2617558B2 (en
Inventor
Kazukuni Tsukuda
一訓 佃
Shiyuuji Takana
周治 高名
Akira Ogasawara
章 小笠原
Yasuhiko Makino
牧野 康彦
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 JP1032080A priority Critical patent/JP2617558B2/en
Priority to MYPI90000151A priority patent/MY105542A/en
Priority to PH39986A priority patent/PH26743A/en
Priority to GB9002531A priority patent/GB2229460B/en
Publication of JPH02212599A publication Critical patent/JPH02212599A/en
Priority to HK57394A priority patent/HK57394A/en
Application granted granted Critical
Publication of JP2617558B2 publication Critical patent/JP2617558B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/94Mixtures with anionic, cationic or non-ionic compounds
    • 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
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • 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
    • C11D3/395Bleaching agents
    • C11D3/3956Liquid compositions
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • C11D1/10Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates thereof
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/92Sulfobetaines ; Sulfitobetaines

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  • Chemical & Material Sciences (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 obtain the title composition excellent both in cleaning and bleaching power and in storage stability by mixing a sulfobetaine ampholytic surface active agent, an amine oxide compound, an alkali metal salt of an alkylsarcosine, an alkali metal salt of hypochlorous acid, and an alkaline substance. CONSTITUTION:The title composition comprises 0.01-10wt.% sulfobetaine ampholytic surface active agent of formula I (wherein R1 is 8-22C alkyl; R2 and R3 are each 1-2C alkyl; n is 2 or 3); 0.1-5wt.% amine oxide compound of formula II (wherein R4 is 8-20C alkyl; R5 and R6 are each 1-3C alkyl); 0.1-6wt.% alkali metal salt of an 8-18C saturated fatty acid or of a 10-18C alkylsarcosine; 0.5-10wt.% alkali metal salt of hypochlorous acid; and 0.1-10wt.% alkaline substance. This composition has moderate viscosity and is excellent both in cleaning and bleaching power and in storage stability.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は洗浄漂白刃及び貯蔵安定性に優れた液体洗浄漂
白剤組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a cleaning bleach blade and a liquid cleaning bleach composition with excellent storage stability.

〔従来の技術及びその課題〕[Conventional technology and its problems]

従来より、次亜塩素酸アルカリ金属塩を主基剤とする洗
浄漂白剤組成物は多く知られている。
BACKGROUND ART Conventionally, many cleaning bleach compositions containing an alkali metal hypochlorite as a main base have been known.

それらの組成物には、洗浄助剤となる界面活性剤として
、次亜塩素酸アルカリ金属塩水溶液に対する溶解性や、
次亜塩素酸アルカリ金属塩水溶液中での有効塩素の安定
性等からポリオキシエチレンアルキルフェニルエーテル
又はアルキルジフェニルエーテルの硫酸化物のアルカリ
金属塩(例えば特開昭52−69415)、パラフィン
スルホネート (例えば特開昭54−148006)等
のアニオン性界面活性剤が使用されてきた。
As a surfactant as a cleaning aid, these compositions have a high solubility in an aqueous solution of alkali metal hypochlorite,
Due to the stability of available chlorine in an aqueous solution of alkali metal hypochlorite, alkali metal salts of sulfates of polyoxyethylene alkylphenyl ethers or alkyldiphenyl ethers (e.g., JP-A-52-69415), paraffin sulfonates (e.g., JP-A-52-69415), Anionic surfactants such as (Sho 54-148006) have been used.

又、アニオン性界面活性剤以外のものでもカルボベタイ
ン系の両性界面活性剤(例えば英国特許第132908
6号、オランダ国特許第148103号、特開昭60−
33300)などが選択されてきた。これらの界面活性
剤の添加により洗浄液の表面活性化能が改善され、洗浄
力は向上するが、未だに充分とは言い難い。
In addition to anionic surfactants, carbobetaine-based amphoteric surfactants (for example, British Patent No. 132908)
No. 6, Dutch Patent No. 148103, JP-A-60-
33300) etc. have been selected. Although the addition of these surfactants improves the surface activation ability of the cleaning solution and improves the cleaning power, it is still far from being sufficient.

また、従来の液体洗浄漂白剤組成物は粘度が低く、斜面
、垂直面での滞留性が劣るため洗浄剤の洗浄力を十分に
発揮するまでには至っていない。
In addition, conventional liquid cleaning bleach compositions have low viscosity and poor retention on slopes and vertical surfaces, so they have not been able to fully demonstrate the cleaning power of the detergent.

斜面、垂直面での滞留性を向上させるため、次亜塩素酸
アルカリ金属塩を増粘させる種々の手段が講じられてき
た。例えば、アクパルジャイト、モンモリロナイトなど
の水和性アルミニウム、マグネシウムのシリケートを使
用する方法(例えば特開昭57−168999)、セビ
オライト系粘土鉱物を使用する方法(例えば特公昭6l
−21969)などの無機系の増粘剤を使用する方法が
挙げられるが、前者は、有効塩素の保持及び強アルカリ
下での長期保存安定性が良くな(、後者においてはセビ
オライト自体が粘土色(黄土色)を呈しており、外観の
上で好ましくなく、また、長期保存安定性も優れたもの
とはいえない。
In order to improve retention on slopes and vertical surfaces, various measures have been taken to increase the viscosity of alkali metal hypochlorite. For example, a method using hydrated aluminum or magnesium silicates such as acpulgite or montmorillonite (e.g., JP-A-57-168999), a method using seviolite clay minerals (e.g., JP-A-57-168999);
-21969), but the former has poor retention of available chlorine and long-term storage stability under strong alkali (in the latter, Seviolite itself is clay-colored. (ocher color), which is not desirable in terms of appearance, and also cannot be said to have excellent long-term storage stability.

有機系増粘剤としては、ポリビニルアルコール、メチル
セルロース、ポリアクリル酸塩、キサンタンガムなどの
水溶性高分子化合物が一般的に用いられるが、有効塩素
の保持及び長期保存安定性において優れたものとはいえ
ないのが実状である。
Water-soluble polymer compounds such as polyvinyl alcohol, methylcellulose, polyacrylates, and xanthan gum are generally used as organic thickeners, but although they are excellent in terms of effective chlorine retention and long-term storage stability, The reality is that there is no such thing.

C課題を解決するための手段〕 本発明者らは、適度な粘性を存し、次亜塩素酸アルカリ
金属塩の安定性を損なわず、しかも長期間保存において
も外観の安定性に優れた液体洗浄剤を見出すべく鋭意検
討を行った結果、下記の特定成分の組合せによりその目
的を達成できることを見出し、本発明を完成するに至っ
た。
Means for Solving Problem C] The present inventors have developed a liquid that has appropriate viscosity, does not impair the stability of alkali metal hypochlorite, and has excellent appearance stability even during long-term storage. As a result of intensive research to find a cleaning agent, it was discovered that the objective could be achieved by a combination of the following specific components, and the present invention was completed.

即ち本発明は、 (a)−最大 (式中、R+は炭素数8〜22のアルキル基、RZ、 
Riは炭素数1〜2のアルキル基、nは2〜3の整数を
示す。)で表されるスルホベタイン型両性界面活性剤を
0.01〜10重量% (b)−最大   R4RSR,NH3(■)(式中、
R4は炭素数8〜20のアルキル基、R,、R。
That is, the present invention provides (a)-maximum (wherein R+ is an alkyl group having 8 to 22 carbon atoms, RZ,
Ri represents an alkyl group having 1 to 2 carbon atoms, and n represents an integer of 2 to 3. ) 0.01 to 10% by weight of a sulfobetaine type amphoteric surfactant (b) - Maximum R4RSR,NH3(■) (in the formula,
R4 is an alkyl group having 8 to 20 carbon atoms, R,,R.

は炭素数1〜3のアルキル基を示す。)で表されるアミ
ンオキサイド化合物を0.1〜5重景重合C)炭素数8
〜18の飽和脂肪酸または炭素数10〜18のアルキル
サルコシンのアルカリ金属塩を0.1〜6重量% (d)次亜塩素酸アルカリ金属塩を0.5〜10重景%
重合)アルカリ性を呈する物質を0.1〜10重量%含
有することを特徴とする液体洗浄漂白剤組成物を提供す
るものである。
represents an alkyl group having 1 to 3 carbon atoms. ) C) Carbon number 8
0.1 to 6% by weight of an alkali metal salt of ~18 saturated fatty acids or alkylsarcosine having 10 to 18 carbon atoms (d) 0.5 to 10% of an alkali metal salt of hypochlorite
The present invention provides a liquid cleaning bleach composition characterized by containing 0.1 to 10% by weight of a substance exhibiting alkalinity (polymerization).

上記−最大(I)において、R9は炭素数8〜22のア
ルキル基であり、炭素数12〜18のアルキル基が好ま
しい。R,、R,は炭素数1〜2のアルキル基であり、
このうち炭素数1のメチル基が好ましい。nは2〜3の
整数であるが、このうち3のものが好ましい。
In the above-mentioned maximum (I), R9 is an alkyl group having 8 to 22 carbon atoms, preferably an alkyl group having 12 to 18 carbon atoms. R,, R, is an alkyl group having 1 to 2 carbon atoms,
Among these, a methyl group having 1 carbon number is preferred. n is an integer of 2 to 3, preferably 3.

一般式(II)において、R4の炭素数8〜20のアル
キル基としては、オクチル基、デシル基、ドデシル基、
テトラデシル基、ヘキサデシル基、オクタデシル基など
が挙げられる。これらのうち、好ましくはドデシル基及
びテトラデシル基であるが、天然物から誘導された炭素
数の異なるアルキル基の混合物でもかまわない。R,、
R。
In general formula (II), the alkyl group having 8 to 20 carbon atoms for R4 includes an octyl group, a decyl group, a dodecyl group,
Examples include tetradecyl group, hexadecyl group, and octadecyl group. Among these, dodecyl and tetradecyl groups are preferred, but a mixture of alkyl groups having different carbon numbers derived from natural products may also be used. R,,
R.

は炭素数1〜3のアルキル基であり、メチル基、エチル
基、プロピル基などが挙げられるが、これらのうち、好
ましくはメチル基である。
is an alkyl group having 1 to 3 carbon atoms, and examples thereof include a methyl group, an ethyl group, a propyl group, and among these, a methyl group is preferable.

−最大(旧で示されるアミンオキサイド化合物(b)の
具体的な例としては、ラウリルジメチルアミンオキサイ
ド、ミリスチルジメチルアミンオキサイド、ヤシジメチ
ルアミンオキサイドなどが挙げられる。
Specific examples of the amine oxide compound (b) represented by - maximum (old) include lauryl dimethyl amine oxide, myristyl dimethyl amine oxide, and coconut dimethyl amine oxide.

炭素数8〜18の飽和脂肪酸または炭素数10〜18の
アルキルサルコシンのアルカリ金属塩(C)としては、
通常ラウリン酸ナトリウム、ラウリルサルコシン酸ナト
リウムなど、及びそれら2種以上の混合物が用いられる
As the alkali metal salt (C) of a saturated fatty acid having 8 to 18 carbon atoms or an alkylsarcosine having 10 to 18 carbon atoms,
Usually, sodium laurate, sodium lauryl sarcosinate, etc., and mixtures of two or more thereof are used.

次亜塩素酸アルカリ金属塩(d)としては、通常次亜塩
素酸ナトリウムが用いられる。
As the alkali metal hypochlorite salt (d), sodium hypochlorite is usually used.

アルカリ性を呈する物質(e)としては、水酸化ナトリ
ウム、炭酸ナトリウム、メタ珪酸ナトリウム、三燐酸ナ
トリウムなどが挙げられ、これらのうち、水酸化ナトリ
ウムが好ましい。
Examples of the substance (e) exhibiting alkalinity include sodium hydroxide, sodium carbonate, sodium metasilicate, sodium triphosphate, etc. Among these, sodium hydroxide is preferred.

本発明の液体洗浄漂白剤組成物におけるスルホベタイン
型両性界面活性剤(a)の含有量は0.01〜10重量
%、好ましくは0.03〜5重量%の範囲である。スル
ホベタイン型両性界面活性剤の含有量が0.01重量%
未満になると組成物の保存安定性が悪くなる。また10
重量%を越える含有量は実際上必要としない。
The content of the sulfobetaine type amphoteric surfactant (a) in the liquid cleaning bleach composition of the present invention ranges from 0.01 to 10% by weight, preferably from 0.03 to 5% by weight. Content of sulfobetaine type amphoteric surfactant is 0.01% by weight
When the amount is less than that, the storage stability of the composition deteriorates. 10 more
Contents exceeding % by weight are practically not required.

アミンオキサイド化合物Cb)の含有量は0.1〜5重
量%、好ましくは0.1〜3重量%の範囲である。アミ
ンオキサイド化合物の含有量が0.1重量%未満になる
と組成物の保存安定性が悪くなり、また5重量%を越え
ると次亜塩素酸アルカリ金属塩の安定性が損なわれる。
The content of amine oxide compound Cb) ranges from 0.1 to 5% by weight, preferably from 0.1 to 3% by weight. If the content of the amine oxide compound is less than 0.1% by weight, the storage stability of the composition will deteriorate, and if it exceeds 5% by weight, the stability of the alkali metal hypochlorite will be impaired.

炭素数8〜18の飽和脂肪酸または炭素数10〜18の
アルキルサルコシンのアルカリ金属塩(C)の含有量は
0.1〜6重量%、好ましくは0.1〜4重量%の範囲
である。炭素数8〜18の飽和脂肪酸または炭素数10
〜18のアルキルサルコシンのアルカリ金属塩の含有量
が0.1重量%未満になると粘度が増大せず、6重量%
を越えると粘度が増大しすぎて使用感が損なわれる。
The content of the alkali metal salt (C) of saturated fatty acid having 8 to 18 carbon atoms or alkyl sarcosine having 10 to 18 carbon atoms is in the range of 0.1 to 6% by weight, preferably 0.1 to 4% by weight. Saturated fatty acids with 8 to 18 carbon atoms or 10 carbon atoms
When the content of the alkali metal salt of ~18 alkyl sarcosine is less than 0.1% by weight, the viscosity does not increase and the content is 6% by weight.
If it exceeds this value, the viscosity will increase too much and the feeling of use will be impaired.

次亜塩素酸アルカリ金属塩(イ)の含有量は0.5〜1
0重量%、好ましくは2〜7重量%の範囲である。次亜
塩素酸アルカリ金属塩の含有量が0.5重量%未満にな
ると漂白刃が不足し、10重量%を越える含有量は実際
上必要としない。
The content of alkali metal hypochlorite (a) is 0.5-1
0% by weight, preferably in the range 2-7% by weight. If the content of alkali metal hypochlorite is less than 0.5% by weight, the bleaching blade will be insufficient, and a content exceeding 10% by weight is not actually required.

アルカリ性を呈する物質(e)の含有量は0.1〜10
重量%、好ましくは0.5〜5重量%の範囲である。
The content of the substance exhibiting alkalinity (e) is 0.1 to 10
% by weight, preferably in the range 0.5-5% by weight.

本発明の液体洗浄漂白剤組成物には、更に通常用いられ
るような添加剤、例えば他の界面活性剤、キレート剤、
香料、着色剤などの成分を配合することができる。
The liquid cleaning bleach composition of the present invention may further contain additives such as those commonly used, such as other surfactants, chelating agents,
Components such as fragrances and coloring agents can be added.

なお、本発明による液体洗浄漂白剤組成物の粘度は通常
5〜2000cp(B型粘度計、20°C)であり、使
用目的に応じて使い分けが可能である。
The viscosity of the liquid cleaning bleach composition according to the present invention is usually 5 to 2000 cp (B-type viscometer, 20°C), and can be used depending on the purpose of use.

〔実施例〕〔Example〕

次に実施例を挙げ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。
Next, the present invention will be explained with reference to Examples, but the present invention is not limited to these Examples.

1〜2  び     1〜7 表−1に示す組成の各液体洗浄漂白剤組成物を調製し、
それぞれの洗浄力、仕上がり感及び低温安定性を下記の
基準に基づいて評価した。
1-2 and 1-7 Prepare each liquid cleaning bleach composition having the composition shown in Table-1,
The detergency, finish feel, and low-temperature stability of each product were evaluated based on the following criteria.

洗浄力、仕上がり感の評価は、被洗浄面として、水を流
しただけでは落ちない汚れが付着している一般家庭の水
洗トイレを選定し、その水洗便器に評価用液体洗浄漂白
剤30gを塗布し、フラッシュによりすすいだ後の便器
表面の状態をみて行った。
For the evaluation of cleaning power and finish, a general household flush toilet with dirt that cannot be removed by simply flushing was selected as the surface to be cleaned, and 30 g of liquid cleaning bleach for evaluation was applied to the flush toilet. The condition of the toilet bowl surface after rinsing with the flush was examined.

〈洗浄力〉 O:汚れが8割以上落ちる Δ:汚れが2〜5割落ちる ×:汚れがほとんど落ちない 〈仕上がり感〉 ○:すすいだ後、水をはじく部分が2割以上Δ:すすい
だ後、水をはじく部分が2〜5割×:すすいだ後、水を
はじく部分が5割以上く低温安定性〉 評価用液体洗浄漂白剤組成物を一20°C〜+20°C
(1サイクル/日)で30日保存した時の組成物の外観
を観察した。
<Cleaning power> O: More than 80% of dirt is removed Δ: 2-50% of dirt is removed ×: Almost no dirt is removed <Finish feeling> ○: After rinsing, the area that repels water is more than 20% Δ: Rinsed After rinsing, the part that repels water is 20 to 50% ×: After rinsing, the part that repels water is 50% or more.
The appearance of the composition was observed when it was stored for 30 days (1 cycle/day).

O:保存前と変化がない。O: No change from before storage.

Δ:若干分離・沈澱がみられる。Δ: Slight separation/precipitation is observed.

×:分離・沈澱がみられる。×: Separation and precipitation are observed.

これらの評価結果を表−1に示す。These evaluation results are shown in Table-1.

3〜4  び    8〜11 表−2に示す各液体洗浄漂白剤組成物を調製し、それぞ
れの液の粘性(液のたれにくさ)及び仕上がり感につい
て下記の基準に基づいて評価した。
3-4 and 8-11 Each liquid cleaning bleach composition shown in Table 2 was prepared, and the viscosity (difficulty of liquid dripping) and finished feel of each liquid were evaluated based on the following criteria.

この時の被洗浄面としては、実施例1〜2及び比較例1
〜7と同様にして選定した水洗トイレの便器を用いた。
The surfaces to be cleaned at this time were Examples 1 to 2 and Comparative Example 1.
A flush toilet bowl selected in the same manner as in 7 was used.

〈液の粘性(液のたれにくさ)〉 評価用液体洗浄漂白剤を主婦30人に使ってもらい、垂
直面での液のたれにくさについて、5段階評価を行い、
その平均値を求めた。
<Liquid viscosity (difficulty in dripping)> Thirty housewives used the liquid cleaning bleach for evaluation, and evaluated it on a five-point scale regarding the difficulty in dripping on vertical surfaces.
The average value was calculated.

5:液がたれにくい 4:液がややたれにくい 3:どちらともいえない 2:液がややたれやすい 1:液がたれやすい 〈仕上がり感〉 評価用液体洗浄漂白剤を用いて、主婦30人に便器を洗
ってもらい、すすいだ後の仕上がり感、その平均値を求 艷について5段階評価を行い、 めた。
5: The liquid does not drip easily 4: The liquid does not drip easily 3: Neither can be said 2: The liquid tends to drip a little 1: The liquid easily drips <Finish feeling> Using the liquid cleaning bleach for evaluation, 30 housewives were asked The participants were asked to wash the toilet bowl, and the results were evaluated on a five-point scale based on the average quality of the finished product after rinsing.

:仕上がり感が良い(艶が出る) ;やや仕上がり感が良い(やや艶が出る):どちらとも
いえない 二あまり仕上がり感が良くない(あまり艶が出ない) 1:仕上がり感が良くない(艶がでない)これらの評価
結果を表−2に示す。
: Good finish (gloss); Slightly good finish (slightly glossy): Neutral 2. Not very good finish (not very glossy) 1: Poor finish (slightly glossy) The results of these evaluations are shown in Table 2.

〔発明の効果〕〔Effect of the invention〕

本発明によれば、汚れの除去効果はもちろん、洗浄後の
仕上がり効果に優れ、更に使用に際して適度な粘性を有
する液体洗浄漂白剤組成物が得られる。
According to the present invention, a liquid cleaning bleach composition can be obtained which not only has an excellent stain removal effect but also has an excellent finishing effect after washing, and further has an appropriate viscosity when used.

又、本発明によって得られた液体洗浄漂白剤組成物は、
貯蔵安定性にも優れている。
Moreover, the liquid cleaning bleach composition obtained by the present invention is
It also has excellent storage stability.

Claims (1)

【特許請求の範囲】 1、(a)一般式 ▲数式、化学式、表等があります▼( I ) (式中、R_1は炭素数8〜22のアルキル基、R_2
、R_3は炭素数1〜2のアルキル基、nは2〜3の整
数を示す。)で表されるスルホベタイン型両性界面活性
剤を0.01〜10重量% (b)一般式R_4R_5R_6N→O(II)(式中、
R_4は炭素数8〜20のアルキル基、R_5、R_6
は炭素数1〜3のアルキル基を示す。)で表されるアミ
ンオキサイド化合物を0.1〜5重量% (c)炭素数8〜18の飽和脂肪酸または炭素数10〜
18のアルキルサルコシンのアルカリ金属塩を0.1〜
6重量% (d)次亜塩素酸アルカリ金属塩を0.5〜10重量%
(e)アルカリ性を呈する物質を0.1〜10重量%含
有することを特徴とする液体洗浄漂白剤組成物。
[Claims] 1. (a) General formula ▲ Numerical formula, chemical formula, table, etc. ▼ (I) (In the formula, R_1 is an alkyl group having 8 to 22 carbon atoms, R_2
, R_3 represents an alkyl group having 1 to 2 carbon atoms, and n represents an integer of 2 to 3. ) 0.01 to 10% by weight of a sulfobetaine type amphoteric surfactant (b) General formula R_4R_5R_6N→O(II) (in the formula,
R_4 is an alkyl group having 8 to 20 carbon atoms, R_5, R_6
represents an alkyl group having 1 to 3 carbon atoms. ) 0.1 to 5% by weight of an amine oxide compound represented by
18 alkyl sarcosine alkali metal salt from 0.1 to
6% by weight (d) 0.5 to 10% by weight of alkali metal hypochlorite
(e) A liquid cleaning bleach composition characterized by containing 0.1 to 10% by weight of a substance exhibiting alkalinity.
JP1032080A 1989-02-10 1989-02-10 Liquid wash bleach composition Expired - Fee Related JP2617558B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP1032080A JP2617558B2 (en) 1989-02-10 1989-02-10 Liquid wash bleach composition
MYPI90000151A MY105542A (en) 1989-02-10 1990-01-31 Liquid detergent bleaching composition.
PH39986A PH26743A (en) 1989-02-10 1990-02-02 Liquid detergent bleaching composition
GB9002531A GB2229460B (en) 1989-02-10 1990-02-05 Liquid detergent bleaching composition
HK57394A HK57394A (en) 1989-02-10 1994-06-04 Liquid detergent bleaching composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1032080A JP2617558B2 (en) 1989-02-10 1989-02-10 Liquid wash bleach composition

Publications (2)

Publication Number Publication Date
JPH02212599A true JPH02212599A (en) 1990-08-23
JP2617558B2 JP2617558B2 (en) 1997-06-04

Family

ID=12348902

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1032080A Expired - Fee Related JP2617558B2 (en) 1989-02-10 1989-02-10 Liquid wash bleach composition

Country Status (5)

Country Link
JP (1) JP2617558B2 (en)
GB (1) GB2229460B (en)
HK (1) HK57394A (en)
MY (1) MY105542A (en)
PH (1) PH26743A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994011484A1 (en) * 1992-11-18 1994-05-26 Kao Corporation Liquid bleach composition
US5827447A (en) * 1991-05-15 1998-10-27 Kao Corporation Liquid bleaching agent composition
JP2001504467A (en) * 1996-11-13 2001-04-03 ザ、プロクター、エンド、ギャンブル、カンパニー Disinfection microemulsion
JP2003055698A (en) * 2001-08-10 2003-02-26 Kobayashi Pharmaceut Co Ltd Slime remover
JP2012219267A (en) * 2011-04-07 2012-11-12 Touki Corp Pasty composition of hypochlorite
CN108467804A (en) * 2018-03-27 2018-08-31 珠海市洁丽雅生物科技有限公司 A kind of Medical sterilization detergent

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69201572T2 (en) * 1991-01-11 1995-12-21 Millipore Corp Process for performing highly effective depositions by capillary electrophoresis.
EP0651051A3 (en) * 1993-10-29 1996-02-28 Clorox Co Gelled hypochlorite-based cleaner.
EP0765377B1 (en) * 1994-06-07 2005-10-05 Reckitt Benckiser Inc. Cleaning compositions thickened with n-alkyl-n-acyl amino acids and myristyl/cetyl dimethyl amine oxides
EP0805198A1 (en) * 1996-05-03 1997-11-05 The Procter & Gamble Company Cleaning compositions
WO2007035009A1 (en) 2005-09-23 2007-03-29 Dc Chemical Co., Ltd. Non-aqueous liquid oxygen bleach composition

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56111300A (en) * 1980-02-08 1981-09-02 Hitachi Ltd Jig for inncircuit tester
JPS61123700A (en) * 1984-11-19 1986-06-11 株式会社 大阪製薬 Sterilizing viscous detergent
JPS63108100A (en) * 1986-08-07 1988-05-12 ザ・クロロックス・カンパニ− Thick hypochlorite composition

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU519631B2 (en) * 1977-11-18 1981-12-17 Unilever Ltd. Liquid bleach compositions

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56111300A (en) * 1980-02-08 1981-09-02 Hitachi Ltd Jig for inncircuit tester
JPS61123700A (en) * 1984-11-19 1986-06-11 株式会社 大阪製薬 Sterilizing viscous detergent
JPS63108100A (en) * 1986-08-07 1988-05-12 ザ・クロロックス・カンパニ− Thick hypochlorite composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5827447A (en) * 1991-05-15 1998-10-27 Kao Corporation Liquid bleaching agent composition
WO1994011484A1 (en) * 1992-11-18 1994-05-26 Kao Corporation Liquid bleach composition
JP2001504467A (en) * 1996-11-13 2001-04-03 ザ、プロクター、エンド、ギャンブル、カンパニー Disinfection microemulsion
JP2003055698A (en) * 2001-08-10 2003-02-26 Kobayashi Pharmaceut Co Ltd Slime remover
JP2012219267A (en) * 2011-04-07 2012-11-12 Touki Corp Pasty composition of hypochlorite
CN108467804A (en) * 2018-03-27 2018-08-31 珠海市洁丽雅生物科技有限公司 A kind of Medical sterilization detergent

Also Published As

Publication number Publication date
GB9002531D0 (en) 1990-04-04
MY105542A (en) 1994-10-31
PH26743A (en) 1992-09-28
JP2617558B2 (en) 1997-06-04
HK57394A (en) 1994-06-17
GB2229460A (en) 1990-09-26
GB2229460B (en) 1992-07-15

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