JPH02279796A - Detergent composition - Google Patents

Detergent composition

Info

Publication number
JPH02279796A
JPH02279796A JP9949789A JP9949789A JPH02279796A JP H02279796 A JPH02279796 A JP H02279796A JP 9949789 A JP9949789 A JP 9949789A JP 9949789 A JP9949789 A JP 9949789A JP H02279796 A JPH02279796 A JP H02279796A
Authority
JP
Japan
Prior art keywords
cleaning
group
alkyl
detergent
carbon atoms
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
JP9949789A
Other languages
Japanese (ja)
Other versions
JPH0668115B2 (en
Inventor
Masaki Tosaka
登坂 正樹
Yasuyuki Fujii
靖之 藤井
Noriyuki Morii
紀行 森井
Katsuhiko Deguchi
勝彦 出口
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 JP1099497A priority Critical patent/JPH0668115B2/en
Priority to MYPI90000546A priority patent/MY105535A/en
Priority to US07/505,480 priority patent/US5096621A/en
Priority to EP19900303840 priority patent/EP0393908A3/en
Publication of JPH02279796A publication Critical patent/JPH02279796A/en
Publication of JPH0668115B2 publication Critical patent/JPH0668115B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the subject compsn. with excellent permeating force and detergency by mixing a nonionic surface active agent with a specified dialkylamine oxide at a specified ratio. CONSTITUTION:A nonionic surface active agent (e.g. polyoxyethylene dodecyl ether) and a dialkylamine oxide of the formula [wherein R1 to 2 are each a 6 to 18C alkyl or alkenyl; R3 is CH2CH2, CH2CH(CH3), CH2CH2CH2; R4 is a 1 to 4C alkyl, hydroxyalkyl, benzyl or H; (n) is 1 to 20] are mixed together at a wt. ratio of 0.01 to 100.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は非イオン性界面活性剤と特定のジアルキルアミ
ンオキサイドを含有し、浸透力に優れ、洗浄力の極めて
良好な洗浄剤組成物に関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a detergent composition containing a nonionic surfactant and a specific dialkylamine oxide, which has excellent penetration power and extremely good detergency. It is.

〔従来の技術) 界面活性剤の基本的な性質として乳化作用、可溶化作用
、分散作用、起泡作用、浸透作用等が挙げられるが、洗
浄剤の一成分として界面活性剤を用いた場合には、これ
らの作用の総合的効果として洗浄力が発現すると考えら
れる。
[Prior art] The basic properties of surfactants include emulsification, solubilization, dispersion, foaming, and penetration. It is thought that detergency is developed as a comprehensive effect of these actions.

これらの作用のうち、浸透作用は、例えば繊維等の洗浄
に際しては繊維が洗浄液で濡れるのを容易にし、繊維間
に付着した汚れに洗浄成分が作用し易くすると考えられ
る。また食器、調理器具等の硬質表面の洗浄に際しては
被洗浄物の濡れ性を改善し、油性汚れを落ち易くするの
みならず、汚れの被洗浄物への再付着を抑制する働きが
あると考えられる。
Among these effects, the penetrating effect is thought to make it easier for the fibers to be wetted with a cleaning liquid when cleaning fibers, etc., and to make it easier for the cleaning ingredients to act on dirt adhering between the fibers. In addition, when cleaning hard surfaces such as tableware and cooking utensils, it is believed that it not only improves the wettability of the object to be cleaned and makes it easier to remove oily stains, but also suppresses the re-adhesion of stains to the object being cleaned. It will be done.

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

浸透作用の強い界面活性剤としては、スルホコハク酸−
’;−2−エチルヘキシルエステルナトリウム塩(商品
名:エアロゾルOT)が有名であるが、このスルホコハ
ク酸−ジー2−エチルヘキシルエステルナトリウム塩は
陰イオン性界面活性剤のため、使用水中の硬度成分の影
響を受けやすく、高硬度の水中では水に難溶のCa塩、
Mg塩を生成するため、強い浸透作用を発揮し得ない。
Sulfosuccinic acid is a surfactant with strong penetrating action.
-2-Ethylhexyl ester sodium salt (product name: Aerosol OT) is famous, but since this sulfosuccinic acid di-2-ethylhexyl ester sodium salt is an anionic surfactant, it is affected by the hardness components in the water used. Ca salt, which is easily susceptible and poorly soluble in water with high hardness,
Because it produces Mg salts, it cannot exhibit strong penetrating action.

また分子内にエステル結合を持つため、耐アルカリ性が
悪いという問題があり、衣料用重質洗剤に通常用いられ
ているアルカリビルダーと併用すると分解する恐れがあ
る。またこれを食器用洗剤等の液体洗浄剤に用いる場合
、水に対する溶解度が低く、液晶を形成し易いため高濃
度の液体組成物が得難いといった欠点があった。このた
め、強い浸透作用の洗浄力への寄与が期待できるにもか
かわらず、洗浄基剤として活用し得なかった。
Furthermore, since it has an ester bond in its molecule, it has a problem of poor alkali resistance, and there is a risk that it will decompose if used in combination with an alkali builder commonly used in heavy-duty laundry detergents. Furthermore, when this is used in liquid cleaning agents such as dishwashing detergents, it has the disadvantage that it has low solubility in water and tends to form liquid crystals, making it difficult to obtain a highly concentrated liquid composition. For this reason, it has not been possible to utilize it as a cleaning base, even though its strong penetrating action can be expected to contribute to cleaning power.

〔課題を解決するための手段〕[Means to solve the problem]

斯かる実情において本発明者らは、浸透性に優れた洗浄
基剤を開発せんと鋭意研究した結果、特定のアルキルア
ミンオキサイドが、スルホコハク酸−ジー2−エチルヘ
キシルエステルナトリウム塩に匹敵する強い浸透力を有
し、特定の非イオン性界面活性剤との組合せにおいて良
好な洗浄力を発揮することを見出し、本発明を完成する
に至った。
Under these circumstances, the present inventors conducted intensive research to develop a cleaning base with excellent permeability, and as a result, a specific alkylamine oxide has a strong permeability comparable to that of sulfosuccinic acid di-2-ethylhexyl ester sodium salt. The present inventors have discovered that they exhibit good detergency when combined with a specific nonionic surfactant, and have completed the present invention.

すなわち本発明は、 (a)非イオン性界面活性剤と、 (b)一般式(I)で表されるジアルキルアミンオキサ
イドを含有し、(a) / (b)重量比が0.01〜
100であることを特徴とする洗浄剤組成物を提供する
ものである。
That is, the present invention contains (a) a nonionic surfactant and (b) a dialkylamine oxide represented by the general formula (I), and the (a) / (b) weight ratio is 0.01 to
The present invention provides a cleaning composition characterized in that:

p。p.

Φ (式中、R+、Rtはそれぞれ炭素数6〜18のアルキ
ル基またはアルケニル基を表し、R1は−CHzCHz
−1−CHzCH(CH+)−1−CHtCHzCH*
−、またはこれらの混合物を表し、R4は炭素数1〜4
のアルキル基、ヒドロキシアルキル基、ベンジル基、ま
たは水素原子を表し、nは1〜20、好ましくは2〜1
0、特に好ましくは2〜5の数を表す。) 本発明に用いられる成分(a)の非イオン性界面活性剤
は成分(b)との相溶性や経済性等が良好なものならば
いずれのものを用いても良(、特に限定されるものでは
ない。(a)成分として好適なも□のを以下に例示する
Φ (In the formula, R+ and Rt each represent an alkyl group or an alkenyl group having 6 to 18 carbon atoms, and R1 is -CHzCHz
-1-CHzCH(CH+)-1-CHtCHzCH*
-, or a mixture thereof, R4 has 1 to 4 carbon atoms
represents an alkyl group, hydroxyalkyl group, benzyl group, or hydrogen atom, and n is 1 to 20, preferably 2 to 1
0, particularly preferably a number from 2 to 5. ) Any nonionic surfactant as component (a) used in the present invention may be used as long as it has good compatibility with component (b) and economical efficiency (although there are no particular limitations). Examples of suitable components as component (a) are shown below.

(I)一般式(n)で表されるポリオキシアルキレンア
ルキルフェニルエーテル。
(I) Polyoxyalkylene alkylphenyl ether represented by general formula (n).

式中、R2は炭素数10〜18のアルキル基またはアル
ケニル基を表し、R3は一般式(I)と同じで、mは3
〜40の数を表す。
In the formula, R2 represents an alkyl group or alkenyl group having 10 to 18 carbon atoms, R3 is the same as in general formula (I), and m is 3
Represents the number ~40.

(2)一般式(II[)で表されるポリオキシアルキレ
ンアルキルエーテル。
(2) Polyoxyalkylene alkyl ether represented by general formula (II[).

R&0(R30)、H(III ) 式中、R1は炭素数10〜18のアルキル基またはアル
ケニル基を表し、R3は一般式(I) と同じで、mは
3〜40の数を表す。
R&0(R30), H(III) In the formula, R1 represents an alkyl group or alkenyl group having 10 to 18 carbon atoms, R3 is the same as in general formula (I), and m represents a number from 3 to 40.

(3)一般式(IV)または(V)で表される高級脂肪
酸アルカノールアミド。
(3) Higher fatty acid alkanolamide represented by general formula (IV) or (V).

式中、R1は炭素数7〜23のアルキル基またはアルケ
ニル基を表す。
In the formula, R1 represents an alkyl group or an alkenyl group having 7 to 23 carbon atoms.

(4)一般式(Vl)で表されるアルキルグリコシド。(4) Alkyl glycoside represented by general formula (Vl).

Rm(OR*)xG、             (V
l )式中、R1は直鎖または分岐鎖の炭素数8〜18
のアルキル基、アルケニル基またはアルキルフェニル基
を表し、R9は炭素数2〜4のアルキレン基を表し、G
は炭素数5〜6を有する還元糖に由来する残基である。
Rm(OR*)xG, (V
l) In the formula, R1 is a straight chain or branched chain having 8 to 18 carbon atoms.
represents an alkyl group, alkenyl group or alkylphenyl group, R9 represents an alkylene group having 2 to 4 carbon atoms, and G
is a residue derived from a reducing sugar having 5 to 6 carbon atoms.

 Xはその平均値がO〜5、好ましくはO〜2であり、
yはその平均値が1〜10、好ましくは1.1〜3であ
る。炭素数5〜6を有する還元糖としては、グルコース
、ガラクトース、キシロース、マンノース、リキソース
、アラビノース、マルトース、キシロビオース、イソマ
ルトース、セロビオース、ゲンチビオース、ラクトース
、スクロース、ニゲロース、ツラノース、ラフィノース
、ゲンチビオース、メレジトース等が挙げられる。
The average value of X is O~5, preferably O~2,
The average value of y is 1 to 10, preferably 1.1 to 3. Examples of reducing sugars having 5 to 6 carbon atoms include glucose, galactose, xylose, mannose, lyxose, arabinose, maltose, xylobiose, isomaltose, cellobiose, gentibiose, lactose, sucrose, nigerose, turanose, raffinose, gentibiose, melezitose, etc. Can be mentioned.

(5)ポリプロピレングリコールの分子量が1000〜
4000でポリエチレンオキサイド平均付加モル数が1
0〜60のポリプロピレングリコール・ポリエチレンオ
キサイド付加物。
(5) The molecular weight of polypropylene glycol is 1000~
4000, the average number of added moles of polyethylene oxide is 1
0 to 60 polypropylene glycol/polyethylene oxide adduct.

本発明に用いられる成分Φ)のジアルキルアミンオキサ
イドは、単独でも高い浸透力を示すものの、水に対する
溶解度が低く、単独では洗浄力は充分とはいえない。溶
解性の向上には(a)/(ハ)重量比が0.01以上で
あることが必要である。
Although dialkylamine oxide, component Φ) used in the present invention, shows high penetrating power even when used alone, it has low solubility in water and cannot be said to have sufficient detergency when used alone. In order to improve solubility, it is necessary that the weight ratio (a)/(c) is 0.01 or more.

ジアルキルアミンオキサイドは成分(a)を主成分とす
る洗浄剤組成物中に少量含有させただけで強い浸透作用
を現し、洗浄力を向上させるが、(a) / (b)重
量比が100を越えるとその効果は著しく減少し好まし
くない。このため、(a) / (b)重量比は0゜0
1〜100の範囲内、好ましくはo、i〜10の範囲内
にあることが必要である。
Dialkylamine oxide exhibits a strong penetrating action and improves detergency even when contained in a small amount of a detergent composition containing component (a) as the main component, but when the (a)/(b) weight ratio is less than 100, If it exceeds this, the effect will be significantly reduced and this is not preferable. Therefore, the (a) / (b) weight ratio is 0°0
It needs to be within the range of 1 to 100, preferably within the range of o, i to 10.

本発明の洗浄剤組成物は液体、ペースト状、固体、粉末
等の形態をとり得るが、使い易さの点では液体または粉
末状の形態とするのが望ましい。
The cleaning composition of the present invention can take the form of liquid, paste, solid, powder, etc., but from the viewpoint of ease of use, it is preferably in liquid or powder form.

本発明の洗浄剤組成物は主として食器、調理器具等の洗
浄や衣料の洗浄に供されるが、この他にも浴槽、浴室、
床、壁、窓ガラス、家具、便器等の住居回りの洗浄剤等
にも適用することができ、用途は特に限定されない。
The cleaning composition of the present invention is mainly used for cleaning dishes, cooking utensils, etc., and for cleaning clothes, but it can also be used for cleaning bathtubs, bathrooms, etc.
It can also be applied as a cleaning agent for areas around the house such as floors, walls, window glass, furniture, toilet bowls, etc., and the use is not particularly limited.

本発明の洗浄剤組成物には上記の必須成分の他に、目的
とする性能を損なわない範囲で必要に応じて種々の成分
を配合することができ、例えば界面活性剤として、直鎖
アルキルベンゼンスルホン酸塩、ポリオキシエチレンア
ルキルエーテル硫酸塩、アルキル硫酸塩、α−オレフィ
ンスルホン酸塩、アルカンスルホン酸塩、ατスルホ脂
肪酸エステル等の陰イオン性界面活性剤;ベタイン、ス
ルホベタイン等の両性界面活性剤が挙げられる。
In addition to the above-mentioned essential components, the cleaning composition of the present invention may contain various components as necessary within a range that does not impair the desired performance. For example, as a surfactant, linear alkylbenzene sulfone Anionic surfactants such as acid salts, polyoxyethylene alkyl ether sulfates, alkyl sulfates, α-olefin sulfonates, alkanesulfonates, ατ sulfo fatty acid esters; Ampholytic surfactants such as betaine and sulfobetaine can be mentioned.

また、液体洗浄剤に用いられる可溶化剤としては、エタ
ノール、イソプロパツール等の低級アルコール類;エチ
レングリコール、プロピレングリコール、グリセリン、
ソルビトール等の多価アルコール類;p−)ルエンスル
ホン酸塩、m−キシレンスルホン酸塩等の芳香族スルホ
ン酸塩類が挙げられる。更に、ビルグーとしては、硫酸
ナトリウム、縮合リン酸塩、合成ゼオライト、エチレン
ジアミン四酢酸(EDT^)、ニトリロ三酢酸(NTA
)等の硬水軟化剤;ケイ酸塩、炭酸塩、苛性ソーダ、エ
タノールアミン等の無機・有機アルカリ剤;カルボキシ
メチルセルロース、ポリエチレングリコール等の再汚染
防止剤等が挙げられる。
In addition, solubilizing agents used in liquid cleaning agents include lower alcohols such as ethanol and isopropanol; ethylene glycol, propylene glycol, glycerin,
Polyhydric alcohols such as sorbitol; aromatic sulfonates such as p-)luenesulfonate and m-xylenesulfonate. Furthermore, as bilgu, sodium sulfate, condensed phosphate, synthetic zeolite, ethylenediaminetetraacetic acid (EDT^), nitrilotriacetic acid (NTA
), inorganic/organic alkaline agents such as silicates, carbonates, caustic soda, ethanolamine, etc.; recontamination preventive agents such as carboxymethyl cellulose, polyethylene glycol, etc.

その他にも酵素、研磨剤、蛍光染料、着色料、保存料、
香料等を目的に応じて配合することができる。
In addition, enzymes, abrasives, fluorescent dyes, colorants, preservatives,
Flavors and the like can be added depending on the purpose.

〔実施例〕〔Example〕

以下実施例にて本発明の詳細な説明するが、本発明はこ
れらの実施例に限定されるもではない。
The present invention will be described in detail below with reference to Examples, but the present invention is not limited to these Examples.

実施例1 表−1に示す各種組成物を調製し、それぞれの浸透力及
び洗浄力を下記の方法により調べた。
Example 1 Various compositions shown in Table 1 were prepared, and their penetrating power and detergency were examined by the following methods.

く浸透力試験 (I)〉 試験片の作成: 牛脂とナタネ油とを重量比9/1で混合したモデル汚れ
を融点以上(約50°C)に加熱し、バーコーダ−を用
いてステンレスプレート(I5CllX20C11)に
均一に塗布した。この時、塗布面のモデル汚れの厚さは
、プレートを25℃に冷却し、油が固化した状態で20
±3−となるようにした。
Penetration test (I)〉 Preparation of test piece: A model stain made by mixing beef tallow and rapeseed oil at a weight ratio of 9/1 was heated to above the melting point (approximately 50°C), and a stainless steel plate ( I5CllX20C11). At this time, the thickness of the model stain on the applied surface is 20°C when the plate is cooled to 25°C and the oil solidifies.
It was set to be ±3-.

上記のようにして調製した試験片に、図−1のようにオ
シロスコープを接続し、洗剤水溶液を図−1の3の部分
に0.051d滴下して洗剤水溶液が油層を浸透し、ス
テンレスプレートに達するまでの時間を下記の条件で測
定した。
An oscilloscope was connected to the test piece prepared as above as shown in Figure 1, and an aqueous detergent solution was dropped for 0.051 d onto the area marked 3 in Figure 1. The time taken to reach this point was measured under the following conditions.

I主粂止 洗剤濃度? 0.15重量% 使用水の硬度:4°DH 温    度:25 °C く洗浄力試験 (I)〉 JISに3370−1979の4.9「台所用合成洗剤
洗浄力試験法」に準拠し、下記の条件で測定した。
I Main detergent concentration? 0.15% by weight Hardness of water used: 4°DH Temperature: 25°C Detergent power test (I)> Based on JIS 3370-1979 4.9 "Detergent power test method for kitchen synthetic detergents", Measurement was performed under the following conditions.

貫主粂止 洗剤濃度:0.15重量% 使用水の硬度:4°DH 温    度:25 ℃ 洗浄時間810分間 モデル汚れの組成:牛脂/ナタネ油−9/1(重量比) 洗浄力の判定: 洗浄前後の被洗浄物(スライドグラス)の重量変化から
洗浄率を算出した。
Detergent concentration: 0.15% by weight Hardness of water used: 4°DH Temperature: 25°C Cleaning time: 810 minutes Composition of model soil: Beef tallow/rapeseed oil - 9/1 (weight ratio) Judgment of cleaning power: The cleaning rate was calculated from the change in weight of the object to be cleaned (slide glass) before and after cleaning.

これらの結果を表−1に示す。These results are shown in Table-1.

実施例2 表−2に示す組成物を調製し、それぞれの浸透力及び洗
浄力を下記の方法により稠べた。
Example 2 Compositions shown in Table 2 were prepared, and the penetration power and detergency of each composition was determined by the following method.

その結果を表−4に示す。The results are shown in Table 4.

表−2 ジアルキルアミンオキサイドとしては一触式(I)で表
される化合物のR3−R4及びnがそれぞれ表−4に示
すようなものを用いた。
Table 2 As dialkylamine oxides, compounds represented by the monocatalytic formula (I) in which R3-R4 and n are shown in Table 4 were used.

〈浸透力試験 (2)〉 100 dビーカーに洗剤水溶液100 dを入れ、そ
の水面に2CIlX2C11の未精練の乾燥したフェル
トを静かに浮かべ、フェルトがビーカーの底まで沈降す
るのに要する時間を以下の条件で測定した。
<Penetration power test (2)> Pour 100 d of detergent aqueous solution into a 100 d beaker, gently float unrefined dry felt of 2CIlX2C11 on the water surface, and calculate the time required for the felt to settle to the bottom of the beaker as follows. Measured under the following conditions.

皿主粂往 洗剤濃度:O,tS重量% 使用水の硬度:4°OH 温    度;25 °C く洗浄力試験 (2)〉 洗剤水溶液11に表−3に示す組成の人工汚垢を付着さ
せたIOcIIXIOcImの人工汚染布12枚を入れ
、浴比が1/60になるように同一サイズの汚染してい
ない布を更に加え、ターボトメ−ターにて1100rp
で以下の条件にて洗浄した。
Detergent concentration: O, tS wt% Hardness of water used: 4°OH Temperature: 25 °C Cleaning power test (2)> Artificial dirt with the composition shown in Table 3 was attached to detergent aqueous solution 11. Add 12 artificially contaminated cloths of IOcIIXIOcIm, add uncontaminated cloths of the same size so that the bath ratio is 1/60, and heat at 1100 rpm in a turbotometer.
Washing was carried out under the following conditions.

皿主矢止 洗剤濃度: 0.15重量% 使用水の硬度:4’DH 温    度:25  °C 洗浄時間;10分間 すすぎ:4”DH硬水にて5分間 人工汚染布の人工汚垢の組成: 表−3 洗浄力の判定; 洗浄力は汚染(インジケーターとしてカーボンブラック
を常法により混入)前の原布及び洗浄前後の汚染布の反
射率を自記色彩計(島津製作所製)にて測定し、次式に
よって洗浄率を求めた0表−4には汚染布12枚の測定
平均値を示した。
Dishwashing detergent concentration: 0.15% by weight Hardness of water used: 4'DH Temperature: 25 °C Washing time: 10 minutes Rinse: 5 minutes with 4''DH hard water Composition of artificial stains on artificially contaminated cloth : Table-3 Judgment of detergency; The detergency was determined by measuring the reflectance of the original cloth before contamination (carbon black was mixed in as an indicator by a conventional method) and the contaminated cloth before and after washing using a self-recording colorimeter (manufactured by Shimadzu Corporation). The cleaning rate was calculated using the following formula. Table 4 shows the average value measured for 12 contaminated cloths.

洗浄率(%)− 実施例3 表−5に示す洗剤(A)(比較品)及び洗剤(B)(本
発明品)を調製し、それぞれの浸透力及び洗浄力を調べ
た。浸透力の評価は浸透力試験(2)と同様に行った。
Cleaning rate (%) - Example 3 Detergent (A) (comparative product) and detergent (B) (inventive product) shown in Table 5 were prepared and their penetrating power and detergent power were examined. The evaluation of the penetration power was performed in the same manner as the penetration power test (2).

それらの結果を表−5に示す。The results are shown in Table 5.

く洗浄力試験 (3)〉 汚染布の調製: 綿/テトロン混紡の白生地を9CI!1X30c11に
裁断し、ワイシャツの襟に縫い付け、成年男子に3日間
着用させた。着用後汚染された布を25°C265%R
Hの室に1ケ月放置した。放置後、汚れの程度が同等で
あり、しかも中心線に対し汚れが左右対称な布を選び、
汚れの対称点で布を半裁し、測定に供した。
Cleaning power test (3)〉 Preparation of contaminated cloth: 9CI of cotton/Tetoron blend white cloth! It was cut into 1x30c11 pieces, sewn onto the collar of a dress shirt, and made to be worn by an adult male for 3 days. After wearing, store contaminated cloth at 25°C, 265%R.
It was left in room H for one month. After leaving it for a while, choose a cloth that has the same degree of dirt and is symmetrical about the center line.
The cloth was cut in half at the symmetrical point of the stain and subjected to measurement.

汚染布の洗浄: 上記のようにして調製された汚染布15枚を1組とし、
50口X 50C11の綿布に縫い付け、45−の評価
用洗浄剤組成物を汚染布に均一に塗布し、10分間放置
後、綿製肌着とを合わせて1kgとし、東芝製洗濯機「
銀河」に移し、水道水を加え全量を30!として水温2
5℃、強反転で10分間洗浄し、5分間の溜すすぎを3
回行った後、乾燥し、洗浄力の判定に供した。
Cleaning of contaminated cloth: A set of 15 contaminated cloths prepared as above was prepared.
50 mouths x 50C11 cotton cloth was sewn, a cleaning agent composition for evaluation of 45- was uniformly applied to the contaminated cloth, and after being left for 10 minutes, the total weight including the cotton underwear was 1 kg, and the washing machine manufactured by Toshiba "
Transfer to "Ginga" and add tap water to make the total volume 30! as water temperature 2
Wash at 5°C for 10 minutes with strong inversion, then rinse with water for 5 minutes for 3 times.
After washing several times, it was dried and the detergency was evaluated.

洗浄力の判定: 洗浄力の判定は、(A)、(B) 2種の洗剤で洗浄し
た半裁布を肉眼による一対比較で評価した。評価は、汚
れの程度を表す10段階のランク付けをした標準汚染布
を基準として行った。
Determination of detergency: Determination of detergency was performed by visual comparison of semi-cut fabrics washed with two types of detergents (A) and (B). The evaluation was performed based on a standard contaminated cloth, which was ranked on a 10-level scale representing the degree of soiling.

洗剤(A)の洗浄力を100とした時の洗剤(B)の洗
浄力の点数(洗浄力指数)で洗浄力を表した0点数の差
は0.5以上で有意の差と見なせる。
The difference between 0 points and 0 points, which expresses the detergent power by the detergent power score (detergent power index) of detergent (B) when the detergent power of detergent (A) is 100, is considered to be a significant difference if it is 0.5 or more.

表 る装置の概略図である。table FIG.

ス テンレスプレート 牛脂−ナタネ油塗布膜 試験水溶液滴 電 極 オシロスコープ 注) *2 ジオクチルポリオキシエチレン(5)アミンオキサイド
CsH+v C自Ill?  N−(CToCH□0)、H↓ 4、
Stainless steel plate beef tallow-rapeseed oil coating film test Aqueous solution droplet electrode oscilloscope Note) *2 Dioctyl polyoxyethylene (5) amine oxide CsH+v Cself Ill? N-(CToCH□0), H↓ 4,

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

Claims (1)

【特許請求の範囲】 1(a)非イオン性界面活性剤と、 (b)下記の一般式( I )で表されるジアルキルアミ
ンオキサイドを含有し、(a)成分と(b)成分の重量
比(a)/(b)が0.01〜100であることを特徴
とする洗浄剤組成物。 ▲数式、化学式、表等があります▼( I ) (式中、R_1、R_2はそれぞれ炭素数6〜18のア
ルキル基またはアルケニル基を表し、R_3は−CH_
2CH_2−、−CH_2CH(CH_3)−、−CH
_2CH_2CH_2−、またはこれらの混合物を表し
、R_4は炭素数1〜4のアルキル基、ヒドロキシアル
キル 基、ベンジル基、または水素原子を表し、 nは1〜20の数を表す。) 2(a)非イオン性界面活性剤が、ポリオキシアルキレ
ンアルキルエーテル、ポリオキシアルキレンアルキルフ
ェニルエーテル、高級脂肪酸アルカノールアミド、アル
キルグリコシド及びポリプロピレングリコール・ポリエ
チレンオキサイド付加物からなる群より選ばれる1種ま
たは2種以上である請求項1記載の洗浄剤組成物。
[Claims] 1. Contains (a) a nonionic surfactant, and (b) a dialkylamine oxide represented by the following general formula (I), the weight of component (a) and component (b) A cleaning composition characterized in that the ratio (a)/(b) is 0.01 to 100. ▲There are mathematical formulas, chemical formulas, tables, etc.▼(I) (In the formula, R_1 and R_2 each represent an alkyl group or an alkenyl group having 6 to 18 carbon atoms, and R_3 is -CH_
2CH_2-, -CH_2CH(CH_3)-, -CH
_2CH_2CH_2-, or a mixture thereof, R_4 represents an alkyl group having 1 to 4 carbon atoms, a hydroxyalkyl group, a benzyl group, or a hydrogen atom, and n represents a number of 1 to 20. ) 2(a) The nonionic surfactant is one selected from the group consisting of polyoxyalkylene alkyl ether, polyoxyalkylene alkylphenyl ether, higher fatty acid alkanolamide, alkyl glycoside, and polypropylene glycol polyethylene oxide adduct, or The cleaning composition according to claim 1, which comprises two or more types.
JP1099497A 1989-04-19 1989-04-19 Cleaning composition Expired - Fee Related JPH0668115B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP1099497A JPH0668115B2 (en) 1989-04-19 1989-04-19 Cleaning composition
MYPI90000546A MY105535A (en) 1989-04-19 1990-04-05 Detergent composition.
US07/505,480 US5096621A (en) 1989-04-19 1990-04-06 Detergent composition containing di-long chain alkyl amine oxides
EP19900303840 EP0393908A3 (en) 1989-04-19 1990-04-10 Detergent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1099497A JPH0668115B2 (en) 1989-04-19 1989-04-19 Cleaning composition

Publications (2)

Publication Number Publication Date
JPH02279796A true JPH02279796A (en) 1990-11-15
JPH0668115B2 JPH0668115B2 (en) 1994-08-31

Family

ID=14248929

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1099497A Expired - Fee Related JPH0668115B2 (en) 1989-04-19 1989-04-19 Cleaning composition

Country Status (1)

Country Link
JP (1) JPH0668115B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008075211A (en) * 2006-09-21 2008-04-03 Dai Ichi Kogyo Seiyaku Co Ltd Detergent for textile

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008075211A (en) * 2006-09-21 2008-04-03 Dai Ichi Kogyo Seiyaku Co Ltd Detergent for textile

Also Published As

Publication number Publication date
JPH0668115B2 (en) 1994-08-31

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